 SOLID BITUMEN AT AMBIENT TEMPERATURE
专利摘要:
Granules of material that can be used as a road binder or as a sealing binder comprising a core and a coating layer, in which: the core consists of a first composition comprising at least one material chosen from: a bitumen base, a pitch, a clear binder, and - the coating layer consists of a second composition which comprises: • at least one viscosifying compound selected from cellulose ethers, and • at least one anti-caking agent. Process for producing granules of material that can be used as a road binder or as a sealing binder, as well as their use as a road binder, especially for the manufacture of asphalt mixes. Process for manufacturing asphalt from granules of material that can be used as a road binder or as a sealing binder, and a method for transporting and / or storing and / or handling granules. 公开号:FR3065464A1 申请号:FR1753473 申请日:2017-04-21 公开日:2018-10-26 发明作者:Romain Colliat；Yvong HUNG 申请人:Total Marketing Services SA； IPC主号:
专利说明:
Technical area The present invention relates to granules of a solid material at room temperature, usable as a road binder or as a sealing binder, such as a road bitumen, a pitch, a clear binder, a bitumen / polymer composition. The present invention also relates to a process for the preparation of these granules as well as their use as a road binder, in particular for the manufacture of mixes. The present invention also relates to a process for the manufacture of mixes from the granules according to the invention as well as a method of transport and / or storage and / or handling of these bitumen granules at room temperature, in particular at room temperature. high. State of the art The vast majority of bitumen is used in construction, mainly for the manufacture of road pavements or in industry, for example for roofing applications. It is generally in the form of a highly viscous black material, even solid at room temperature, which becomes fluid when heated. In general, bitumen is stored and transported hot, in bulk, in tankers or by ships at high temperatures in the range of 120 ° C to 160 ° C. However, the storage and transport of hot bitumen has certain drawbacks. On the one hand, the transport of hot bitumen in liquid form is considered dangerous and it is very regulated from a regulatory point of view. This mode of transport does not present any particular difficulties when the transport equipment and infrastructure are in good condition. Otherwise, it can become problematic: if the tanker is not sufficiently insulated, the viscosity of the bitumen may increase during a journey that is too long. Bitumen delivery distances are therefore limited. On the other hand, keeping bitumen at high temperatures in tanks or in tankers consumes energy. In addition, keeping the bitumen at high temperatures for a long time can affect the properties of the bitumen and thus change the final performance of the mix. To overcome the problems of transport and storage of hot bitumen, packaging allowing the transport and storage of bitumen at room temperature has been developed. This mode of transport of bitumen in room temperature conditioning represents only a small fraction of the quantities transported in the world, but it corresponds to very real needs for geographic regions of difficult and expensive access by traditional means of transport. As an example of packaging allowing cold transport currently used, mention may be made of the packaging of bitumen at room temperature in metal drums. ICG70142 FR text deposit 2 This means is increasingly questionable from an environmental point of view because the bitumen stored in barrels must be reheated before its use as a road binder. However, this operation is difficult to implement for this type of packaging and the drums constitute waste after use. On the other hand, the storage of bitumen at room temperature in drums leads to losses because the bitumen is very viscous and part of the product remains on the walls of the drum during transfer to the tanks of the asphalt production units. As for the handling and transportation of bituminous products in these drums, they can be difficult and dangerous if specialized equipment for handling drums is not available from carriers or at the place of use of bitumen. Other examples of packaging include bitumens in the form of granules transported and / or stored in bags, often used in places where the ambient temperature is high. These granules have the advantage of being easy to handle. The same difficulty is encountered in the handling, conditioning and storage of pitches and bituminous compositions comprising, clear binders, bitumen / polymer compositions, in particular the stock solutions of bitumen / polymer compositions. US 3,026,568 describes bitumen granules covered with a powdery material, such as limestone powder. However, this type of bitumen in granules does not prevent the creep of the bitumen, especially at high ambient temperature. Application WO 2009/153324 describes bitumen granules coated with a polymeric anti-caking compound, in particular polyethylene. The disadvantage of this coating is that it modifies the properties of the bitumen during its road application. Application WO 2016/016318 describes bitumen granules comprising a chemical additive. These bitumen granules allow the transport and / or storage and / or handling of the bitumen at room temperature without it leaking, as well as the reduction of their adhesion and agglomeration between them. Application WO 2016/198782 describes bitumens that are solid at room temperature in the form of granules comprising a core and a coating layer in which: the core comprises at least one bitumen base and, - the coating layer comprises at least 10% by mass of one or more viscosifying compounds relative to the total mass of the coating layer, and at least one anti-caking compound. The viscosifying compounds illustrated in WO 2016/198782 are based on gelatin. These granules have satisfactory properties of use, however, they have the disadvantage of requiring an additional step after coating the hearts with the coating layer, to allow the formation of a shell around the hearts. In continuation of its work, the Applicant has surprisingly discovered a new composition of granules of solid material at room temperature, which can be used ICG70142 EN text deposit 3 as road binder or as waterproofing binder, such as road bitumen, pitch, bitumen / polymer composition, clear binder, making it possible to avoid and reduce adhesion and agglomeration during their transport and / or storage and / or handling, at high ambient temperature, over long periods and whose properties are preserved over time compared to the granules of the prior art. More specifically, the Applicant has demonstrated that this new composition of granules makes it possible to resist creep under extreme conditions of transport and / or storage and / or handling, under compression conditions, in particular due to storage, on very long periods. Summary of the invention The subject of the invention is granules of material which can be used as a road binder or as a sealing binder comprising a core and a coating layer in which: the core consists of a first composition comprising at least one material chosen from: a bitumen base, a pitch, a clear binder, and - the coating layer consists of a second composition which comprises: • at least one viscosifying compound chosen from cellulose ethers, and • at least one anti-caking agent. The invention also relates to a method for manufacturing granules of material which can be used as a road binder or as a sealing binder, composed of a core and a coating layer of the core, this method comprising: i) the shaping of the heart from a first composition comprising at least one material chosen from: a bitumen base, a pitch, a clear binder, ii) the coating of the heart on all or part of its surface with a second composition comprising at least one viscosifying compound chosen from cellulose ethers and at least one anti-caking agent. The invention also relates to granules of material which can be used as a road binder or as a waterproofing binder, which can be obtained by implementing this process. According to one embodiment of the invention, the cellulose ether is chosen from: methyl cellulose, ethylcellulose, hydroxymethylcellulose hydroxyethylcellulose (HEC), hydroxypropylcellulose (HPC), hydroxyethyl methylcellulose (HEMC) ), hydroxypropyl methylcellulose (HPMC), hydroxybutyl methylcellulose (HBMC), carboxymethylcellulose (CMC), sodium carboxymethylcellulose (Na-CMC), carboxymethylsulfoethylcellulose, hydroxyethylmethylcarboxymethylcellulose. ICG70142 EN text deposit 4 According to a preferred embodiment of the invention, the cellulose ether is chosen from: hydroxyethyl methylcellulose, hydroxypropyl methylcellulose, hydroxybutyl methylcellulose, even more advantageously hydroxypropyl methylcellulose. According to one embodiment of the invention, the second composition comprises at least 10% of one or more anti-caking agents, the percentages being expressed by mass relative to the total mass of the second composition. According to a preferred embodiment of the invention, the second composition comprises: at least 20% of one or more anti-caking agents, better still at least 30%, advantageously at least 40%, even better at least 50% d one or more anti-caking agents, and optionally one or more plasticizing agents, the percentages being expressed by mass relative to the total mass of the second composition. Preferably, the anti-caking compound is chosen from: talc; fines generally less than 125 µm in diameter, such as siliceous fines, with the exception of limestone fines; sand such as Fontainebleau sand; cement ; carbon; wood residues such as lignin, lignosulfonate, powders of coniferous needles, powders of coniferous cones, in particular pine; rice husk ash; glass powder; clays such as kaolin, bentonite, vermiculite; alumina such as alumina hydrates; silica; silica derivatives such as silica fumes, functionalized silica fumes, in particular hydrophobic or hydrophilic silica fumes, fumed silicas, in particular hydrophobic or hydrophilic fumed silicas, silicates, silicon hydroxides and silicon oxides ; plastic powder; lime; hydrated lime; the plaster ; rubber blowing snow; polymer powder, such as styrene-butadiene copolymers (SB), styrene-butadiene-styrene copolymers (SBS) and mixtures of these materials. According to one embodiment of the invention, the first composition has a needle penetration measured at 25 ° C according to standard EN 1426 from 5 to 330 1/10 mm, preferably from 10 to 220 1/10 mm. According to one embodiment of the invention, the bitumen base further comprises at least one chemical additive chosen from: an organic compound, a paraffin, a polyphosphoric acid, an adhesion dope, and their mixtures. According to one embodiment of the invention, the first composition comprising at least one chemical additive has a penetration of 5 to 45 l / 10mm, measured at 25 ° C according to ICG70142 EN text deposit 5 standard EN 1426 and / or a ball and ring softening temperature greater than or equal to 90 ° C, the ball and ring softening temperature being measured according to standard EN 1427. According to a preferred embodiment, the granules of material which can be used as a road binder or as a sealing binder have stability during transport and / or storage and / or handling at a temperature of up to 100 ° C., advantageously of 20 ° C to 90 ° C, preferably from 20 ° C to 80 ° C, more preferably from 40 ° C to 80 ° C, even more preferably from 40 ° C to 60 ° C, for a period greater than or equal to 2 months, preferably greater than or equal to 3 months. According to a preferred embodiment, in the method of the invention, the second composition is applied to the core of the granules in a fluidized air bed device. The invention also relates to the use of the granules defined above as a road binder. According to a preferred embodiment, the use relates to the manufacture of mixes. The invention also relates to a process for the manufacture of mixes comprising at least one road binder and aggregates, the road binder being chosen from the granules defined above, this process comprising at least the steps of: - heating the aggregates at a temperature ranging from 100 ° C to 180 ° C, preferably from 120 ° C to 160 ° C, - mixing of the aggregates with the road binder in a tank such as a kneader or a kneading drum, - obtaining mixes. According to a preferred embodiment, the asphalt manufacturing process does not include a step of heating the road binder before it is mixed with the aggregates. The invention finally relates to a method of transport and / or storage and / or handling of material usable as road binder or as sealing binder, said material being transported and / or stored and / or handled in the form of granules as defined above. detailed description The objectives which the applicant has set for itself have been achieved by developing compositions of material which can be used as a road binder or as a sealing binder, under a ICG70142 EN filing text 6 divided form, having a core / envelope structure, in which the core is based on a first composition and the coating layer gives the overall structure improved properties under extreme conditions of transport and / or storage and / or handling with respect to the granules of material usable as road binder or as sealing binder known from the prior art. A first object of the invention relates to granules of material which can be used as a road binder or as a sealing binder comprising a core and a coating layer in which: - the core consists of a first composition which comprises at least one material chosen from: a bitumen base, a pitch, a clear binder, and, - the coating layer consists of a second composition which comprises: • at least one viscosifying compound chosen from cellulose ethers, and • at least one anti-caking agent. By "high ambient temperature" is meant the temperature resulting from the climatic conditions under which is transported and / or stored and / or handled the material usable as road binder or as waterproofing binder, in particular road bitumen. More specifically, the high ambient temperature is equivalent to the temperature reached during transport and / or storage of the material which can be used as a road binder or as a sealing binder, in particular road bitumen being less than 100 ° C. Advantageously, the high ambient temperature is from 20 ° C to 90 ° C, preferably from 20 ° C to 80 ° C, more preferably from 40 ° C to 80 ° C, even more preferably from 40 ° C to 60 ° C, it being understood that the high ambient temperature implies that no heat input is provided other than that resulting from the climatic conditions. The invention relates to materials which can be used as road binder or as waterproofing binder, in particular bitumens which can be solid when they are subjected to high ambient temperatures, in particular a temperature of up to 100 ° C., advantageously. , from 20 ° C to 90 ° C, preferably from 20 ° C to 80 ° C, more preferably from 40 ° C to 80 ° C, even more preferably from 40 ° C to 60 ° C. By “material which can be used as a road binder or as a sealing binder” is understood within the meaning of the present invention any material capable of being used for this use, and in particular: bitumen bases, bitumen / polymer compositions, compositions bitumen additive, pitches, bitumen-polymer mother solutions, clear binders, mother solutions clear-polymer binder, mixtures of these materials in all proportions. By "solid material at high ambient temperature" is meant a material having a solid appearance at high ambient temperature under conditions of transport and / or storage and / or handling. More precisely, the term “solid material at high ambient temperature” means a material which retains its solid appearance throughout the transport and / or ICG70142 EN filing text 7 storage and / or handling at high ambient temperature, i.e. a material which does not flow at a temperature of up to 100 ° C, advantageously from 20 ° C to 90 ° C, preferably from 20 ° C to 80 ° C, more preferably from 40 ° C to 80 ° C, even more preferably from 40 ° C to 60 ° C, under its own weight and more, which does not creep when it is subjected to a temperature up to 100 ° C., advantageously, from 20 ° C. to 90 ° C., preferably from 20 ° C. to 80 ° C., more preferably from 40 ° C. to 80 ° C., even more preferably from 40 ° C to 60 ° C, and to pressure forces from the conditions of transport and / or storage and / or handling. By “bitumen solid at room temperature” is meant a bitumen having a solid appearance at room temperature whatever the transport and / or storage conditions. More specifically, the term solid bitumen at room temperature means a bitumen which retains its solid appearance throughout transport and / or storage at room temperature, that is to say a bitumen which does not flow at room temperature under its own weight and more, which does not creep when subjected to pressure forces from transport and / or storage conditions. By “coating layer covering all in part of the surface of the heart”, it is meant that the coating layer covers at least 90% of the surface of the heart, preferably at least 95% of the surface of the heart, more preferably at least 99% of the surface of the heart. The expression “consists essentially of” followed by one or more characteristics, signifies that can be included in the process or the material of the invention, in addition to the components or steps explicitly listed, components or steps which do not significantly modify the properties and characteristics of the invention. The expression "between X and Y" includes the limits. This expression therefore means that the target interval includes the values X, Y and all the values going from X to Y. The composition according to the invention makes it possible to obtain granules of solid material which can be used as a road binder or as a sealing binder, in particular of bitumen, comprising a coating layer which is resistant to climatic conditions and to transport and / or storage of road binders and / or sealing binders, in particular which is resistant to climatic conditions and to the conditions of transport and / or storage of solid road bitumen, which easily breaks under a mechanical shearing effect, such as for example under the effect of mechanical shearing applied in a tank such as a mixer or a drum-mixer during the manufacture of asphalt. More particularly, the coating layer resists the transport and / or storage of road binders and / or sealing binders, in particular bitumen, at room temperature in “Big Bags” while being brittle under the effect of '' mechanical shear. It allows the release of the bitumen core during the manufacture of asphalt. ICG70142 EN text deposit 8 The core of the granules / first composition: First variant: According to a first variant, the cores of the granules of material which can be used as a road binder or as a sealing binder, are prepared from a first bitumen composition comprising one or more bitumen bases. Preferably, the bitumen granules are prepared from a first bitumen composition comprising: - one or more bitumen bases, from 0.1% to 5% by mass, preferably from 0.5% to 4% by mass, more preferably from 0.5% to 2.5% by mass of at least one chemical additive, the percentages being by mass relative to the total basic bitumen mass. The bitumen base and the chemical additive are as described below. Preferably, the bitumen granules are prepared from a first bitumen composition comprising: - one or more bitumen bases, from 0.1% to 5% by mass, preferably from 0.5% to 4% by mass, more preferably from 0.5% to 2.5% by mass of at least one chemical additive and, - from 0.5% to 20% by mass, preferably from 2% to 20% by mass, more preferably from 4% to 15% by mass of at least one anti-caking agent, the percentages being by mass relative to to the total basic bitumen mass. According to a second preferred embodiment, the hearts of the granules are prepared from a first composition comprising: - one or more bitumen bases, between 0.1% and 5% by mass, preferably between 0.5% and 4% by mass, more preferably between 0.5% and 2.5% by mass of at least one chemical additive, - And between 0.05% and 15% by mass, preferably between 0.1% and 10% by mass, more preferably between 0.5% and 6% by mass of at least one olefinic polymeric adjuvant, the percentages being by mass relative to the total basic bitumen mass. According to a third preferred embodiment, the hearts of the granules are prepared from a first composition comprising: - one or more bitumen bases, between 0.1% and 5% by mass, preferably between 0.5% and 4% by mass, more preferably between 0.5% and 2.5% by mass of at least one chemical additive, - and between 0.05% and 15% by mass, preferably between 0.1% and 10% by mass, more preferably between 0.5% and 6% by mass of at least one polymer, ICG70142 EN text deposit 9 the percentages being by mass relative to the total bitumen base mass. Advantageously, the different embodiments described above for the granules can be combined with one another. Second variant: According to a second variant, the cores of the granules of material which can be used as a road binder or as a sealing binder are prepared from a first composition comprising at least one pitch. According to a first embodiment, the hearts of the granules consist of a first composition based on pitch. According to a second embodiment, the cores of the granules consist of a first composition based on pitch and at least one bitumen base. According to an embodiment of this variant, the first composition comprises at least one pitch having a penetrability at 25 ° C ranging from 0 to 20 1/10 mm, a ball and ring softening temperature (TBA) ranging from 115 ° C to 175 ° C, it being understood that the penetrability is measured according to standard EN 1426 and that the TBA is measured according to standard EN 1427. According to one embodiment of this variant, the first composition comprises: - At least one pitch having a penetration at 25 ° C ranging from 0 to 20 1/10 mm, a softening temperature ball and rings (TBA) ranging from 115 ° C to 175 ° C, it being understood that the penetration is measured according to the EN 1426 standard and that the TBA is measured according to the EN 1427 standard, - at least one bitumen base, and - at least one chemical additive. Third variant: According to a third variant, the granules of material which can be used as a road binder or as a sealing binder, are prepared from a first composition comprising at least one clear binder. Conventional bituminous binders, due to the presence of asphaltenes, are black in color and therefore difficult to color. Colored coatings are more and more used because they allow, among other things, to improve the safety of road users by clearly identifying specific lanes such as pedestrian lanes, bicycle paths, bus lanes. They also make it possible to materialize certain danger zones such as agglomeration entrances or dangerous turns. The colored coatings promote visibility in low light conditions, for example at night or in particular sites such as tunnels. Finally, they simply improve the aesthetic appearance of the road ICG70142 EN urban text deposit 10 and can be used for public places, courtyards of buildings and schools, sidewalks, pedestrian streets, walkways of gardens and parks, parking and rest areas. Consequently, for all the abovementioned applications, it is preferred to use clear synthetic binders, not containing asphaltenes and capable of being colored. According to this variant, the first composition comprises at least one clear binder. Advantageously, the first composition comprises at least one base of clear binder and at least one chemical additive chosen from an organic compound, a paraffin, a polyphosphoric acid and their mixtures. According to one embodiment of the invention, the first composition comprises from 0.1% to 5% by mass, preferably from 0.5% to 4% by mass, more preferably from 0.5% to 2.5% by mass of said chemical additive relative to the total mass of said clear additive binder. According to one embodiment of the invention, the first composition comprises - at least one clear binder base, - between 5% and 30% by mass, preferably between 6% and 28% by mass, more preferably between 7% and 26% by mass of the chemical additive (s) relative to the total mass of the said clear binder base. In this case, the first composition is called a concentrated clear binder. According to a preferred embodiment, the granules are prepared from a first composition comprising: - one or more clear binder bases, - from 30 to 40% of at least one polymer, - from 4 to 6% of at least one compatibilizing agent, - from 3% to 15% of at least one anti-caking agent, the percentages being by mass relative to the total mass of the first composition. The term “clear solid binder when cold and in divided form” means a clear binder solid at room temperature which is packaged in a divided form, that is to say in the form of units distinct from one another, which names granules. The clear binder according to the invention is designated indifferently in the present description "clear binder solid when cold and in divided form" or "clear binder with additives". Preferably, the clear binder is a composition which can be used as a substitute for bitumen-based binders for the preparation, for example of colored bituminous mix. A clear binder is free of asphaltenes and can therefore keep the natural color of the aggregate with which it is mixed or be easily colored with pigments. ICG70142 EN text deposit 11 Bitumen base Advantageously, the core or core of the solid bitumen granules according to the invention is prepared from a first composition, which is a composition of road bitumen, said first composition being prepared by bringing into contact: - one or more bitumen bases, and - optionally at least one chemical additive. Within the meaning of the invention, the terms “bitumen” and “road bitumen” are used, in an equivalent manner and independently of one another. By "bitumen" or "road bitumen" is meant all bituminous compositions consisting of one or more bitumen bases and optionally comprising one or more chemical additives, said compositions being intended for road application. Among the bitumen bases which can be used according to the invention, mention may first of all be made of bitumens of natural origin, those contained in deposits of natural bitumen, natural asphalt or the tar sands and the bitumens obtained from the refining of crude oil. . The bitumen bases according to the invention are advantageously chosen from bitumen bases originating from the refining of crude oil. The bitumen bases can be chosen from bitumen bases or mixtures of bitumen bases originating from the refining of crude oil, in particular bitumen bases containing asphaltenes or pitches. Bitumen bases can be obtained by conventional methods of manufacturing bitumen bases in refineries, in particular by direct distillation and / or vacuum distillation of petroleum. These bitumen bases can optionally be visbreaked and / or deasphalted and / or air rectified. It is common to carry out vacuum distillation of atmospheric residues from the atmospheric distillation of crude oil. This manufacturing process therefore corresponds to the succession of atmospheric distillation and vacuum distillation, the feedstock feeding the vacuum distillation corresponding to atmospheric residues. These vacuum residues from the vacuum distillation tower can also be used as bitumens. It is also common to inject air into a feed usually consisting of distillates and heavy products from vacuum distillation of atmospheric residues from petroleum distillation. This process makes it possible to obtain a blown, or semi-blown or oxidized or air-rectified or partially air-rectified base. The different bitumen bases obtained by the refining processes can be combined with each other to obtain the best technical compromise. The bitumen base can also be a bitumen recycling base. Bitumen bases can be hard grade or soft grade bitumen bases. According to the invention, for the conventional methods of manufacturing bitumen bases, the operation is carried out at manufacturing temperatures between 100 ° C and 200 ° C, preferably between 140 ° C and 200 ° C, more preferably between 140 ° C and 170 ° C, and with stirring for a period of at least 10 minutes, preferably between 30 minutes and 10 hours, more ICG70142 EN text deposit 12 preferably between 1 hour and 6 hours. By manufacturing temperature is meant the temperature for heating the bitumen base (s) before mixing as well as the mixing temperature. The temperature and the duration of the heating vary according to the quantity of bitumen used and are defined by the standard NP EN 12594. According to the invention, the blown bitumens can be manufactured in a blowing unit, by passing a flow of air and / or oxygen through a starting bituminous base. This operation can be carried out in the presence of an oxidation catalyst, for example phosphoric acid. Generally, the blowing is carried out at high temperatures, of the order of 200 to 300 ° C., for relatively long periods typically between 30 minutes and 2 hours, continuously or in batches. The blowing time and temperature are adjusted according to the properties targeted for the blown bitumen and according to the quality of the starting bitumen. Preferably, the bitumen base used to manufacture the granules of the invention has a needle penetration measured at 25 ° C according to standard EN 1426 from 5 to 330 1/10 mm, preferably from 10 to 220 1 / 10 mm. As is well known, the so-called “needle penetration” measurement is carried out by means of a standard test NF EN 1426 at 25 ° C. (P25) · This penetration characteristic is expressed in tenths of a millimeter (dmm or 1 / 10 mm). The needle penetration, measured at 25 ° C, according to the standardized test NF EN 1426, represents the measurement of the penetration into a bitumen sample, after a time of 5 seconds, of a needle whose weight with its support is 100 g. The NF EN 1426 standard replaces the NF T 66-004 approved standard of December 1986 with effect from December 20, 1999 (decision of the Director General of AFNOR on November 20, 1999). The base of clear binder The term “clear binder base” is intended to mean compositions comprising a plasticizing agent, for example an oil of petroleum origin or of vegetable origin, a structuring agent, for example a hydrocarbon resin, and a polymer. The composition of the bases of clear binders determines certain essential properties of these binders, in particular the plasticity index, the viscosity of the binder, or the color which must be as clear as possible. According to one embodiment of the invention, the clear binder base comprises: - a plasticizing agent, for example a natural or synthetic oil, devoid of asphaltenes, a structuring agent, for example a hydrocarbon or vegetable resin, - a copolymer, - where appropriate, doping agents, or dopes, or adhesion dopes. ICG70142 EN text submission 13 Clear binder compositions are described in the following patent applications and these clear binder compositions can be used as a clear binder base in the present invention. A clear binder comprising hydrogenated white oils comprising at least 60% paraffinic carbons (according to the ASTM D2140 method) and a hydrocarbon resin can be used as the clear binder base, and a hydrocarbon resin, if appropriate in a mixture with ethylene-acetate type copolymers. vinyl (EVA) or low density polyethylene, for example of the EPDM (ethylene-propylene-diene-monomer) type, as described in WO 01/53409. A clear binder comprising an oil with a naphthenic content between 35% and 80% and a hydrocarbon resin, as described in EP 1783174, can be used as the base of the clear binder. A clear binder comprising a synthetic oil, a resin and a polymer of SBS or SIS type can be used as the clear binder base, as described in EP 1473327. A clear binder comprising: - at least one oil of petroleum origin, preferably an aromatic oil comprising aromatic extracts of petroleum residues, obtained by extraction or de-aromatization of distillation residues from petroleum fractions, at least one resin of plant origin, preferably chosen from rosin esters, glycerol esters and rosin esters, pentaerythritol esters and rosin esters, taken alone or as a mixture, and at least one latex, preferably chosen from latexes of acrylic polymers, natural rubber latexes, synthetic rubber latexes, taken alone or as a mixture, as described in WO 2009/150519. As a clear binder base, a clear synthetic binder can be used comprising: - at least one oil of vegetable origin preferably chosen from rapeseed, sunflower, soybean, flax, olive, palm, castor, wood, corn, squash, grapeseed oils , jojoba, sesame, walnut, hazelnut, almond, shea, macadamia, cotton, alfalfa, rye, safflower, peanut, coconut and coconut, and mixtures thereof, at least one resin of petroleum origin, preferably chosen from resins of petroleum hydrocarbon origin resulting from the copolymerization of aromatic, aliphatic, cyclopentadienic petroleum fractions taken alone or as a mixture and, at least one polymer, preferably chosen from styrene and butadiene copolymers, styrene and isoprene copolymers, ethylene / propene / diene terpolymers, polychloroprenes, ethylene and vinyl acetate copolymers, copolymers ICG70142 EN text deposit 14 of ethylene and methyl acrylate, copolymers of ethylene and butyl acrylate, ethylene / methyl acrylate / glycidyl methacrylate, ethylene / butyl acrylate / maleic anhydride terpolymers, atactic polypropylenes, taken alone or in mixtures, the quantity of oil of vegetable origin in the binder being greater than or equal to 10% by mass and the quantity of polymer in the binder being less than or equal to 15% by mass, as described in WO 2010/055491. According to another embodiment of the invention, the clear binder base comprises: (i) a plasticizing agent consisting of an oil containing a total content of paraffinic compounds, measured according to the ASTM D2140 method, of at least 50%, preferably at least 60% by weight, more preferably between 50% and 90%, preferably between 60% and 80%, and (ii) a copolymer based on conjugated diene units and monovinyl aromatic hydrocarbon units, for example based on butadiene unit and styrene units. Preferably, the oil is a synthetic oil obtained from deasphalting unit cuts (or "CAD oil"). Preferably, the oil contains a total content of paraffinic compounds greater than or equal to 50%, preferably greater than or equal to 60% by weight, and a total content of naphthenic compounds less than or equal to 25% by weight, measured according to the ASTM D2140 method. Preferably, the oil contains a total content of paraffinic compounds greater than or equal to 50%, preferably greater than or equal to 60% by weight, a total content of naphthenic compounds less than or equal to 25% by weight, and a total content in aromatic compounds less than or equal to 25% by weight, measured according to the ASTM D2140 method. For example, the oil contains a total content of paraffinic compounds, measured according to the ASTM D2140 method, of between 50% and 90%, preferably between 60% and 80% by weight, a total content of naphthenic compounds of between 5%. and 25% by weight, and a total content of aromatic compounds of between 5% and 25% by weight. Preferably, the oil has an aniline point, measured according to standard ISO2977: 1997, greater than or equal to 80 ° C, preferably greater than or equal to 90 ° C, for example greater than 100 ° C. Preferably, the clear binder base preferably comprises (i) from 40 to 80% by weight of plasticizing agent, (ii) from 18 to 50% by weight of resin, (iii) from 1 to 7% by weight of copolymer; ICG70142 FR text deposit 15 and, (iv) optionally from 0.05% to 0.5% by weight of adhesive dope, for example of amine, relative to the base weight of clear binder. Advantageously, the clear binder base preferably comprises (i) from 40 to 80% by weight of plasticizing agent, (ii) from 18 to 50% by weight of resin, (iii) from 1 to 7% by weight of copolymer ; and, (iv) from 0.05% to 0.5% by weight of adhesive dope, for example of amine, relative to the base weight of clear binder. Advantageously, the clear binder base also comprises (i) from 45% to 70% by weight of plasticizing agent, (ii) from 25 to 50% by weight of resin, (iii) from 1% to 7% by weight of copolymer; and, (iv) optionally 0.1% and 0.3% by weight of adhesive dope, relative to the total weight of clear binder base. Preferably, the clear binder base essentially consists of (i) from 40 to 80% by weight of plasticizing agent, (ii) from 20 to 50% by weight of resin, (iii) from 1 to 7% by weight of copolymer, based on the total base weight of clear binder. Advantageously, the clear binder base essentially consists of (i) from 40 to 80% by weight of plasticizing agent, (ii) from 20 to 50% by weight of resin, (iii) from 1 to 7% by weight of copolymer and (iv) from 0.05% to 0.5% by weight of adhesion dope, relative to the total weight of clear binder base. Advantageously, the clear binder base essentially also consists of (i) from 45% to 70% by weight of plasticizing agent, (ii) from 25 to 50% by weight of resin (iii) from 1% to 7% by weight copolymer; and, (iv) 0.1% and 0.3% by weight of adhesion dope, based on the total weight of clear binder base. Preferably, the copolymer is a copolymer based on styrene and butadiene units which comprises a content by weight of 1-2 butadiene ranging from 5 to 70%. Preferably, the copolymer is advantageously a copolymer based on styrene and butadiene units which comprises a content by weight of 1-2 butadiene ranging from 5 to 70% and a content by weight of 1,2-vinyl group of between 10 and 40 %. For example, said copolymer based on styrene and butadiene units has a weight-average molecular weight of between 10,000 and 500,000, preferably between 50,000 and 200,000, and more preferably between 50,000 and 150,000 daltons. Preferably, a styrene / butadiene block copolymer or styrene / butadiene / styrene block copolymer will be used. ICG70142 EN text deposit 16 The clear binders according to the invention are advantageously characterized in that they have a color index less than or equal to 4, preferably less than or equal to 3, as determined according to the ASTM DH4 scale. In addition, they can advantageously have a softening temperature Ball-Ring temperature determined according to standard NF EN1427 of between 55 ° C and 90 ° C. Preferably, the clear binder usable according to the invention has a penetrability at 25 ° C, measured according to standard NF EN 1426, of between 10 and 220 1/10 mm, preferably between 30 and 100 1/10 mm, more preferably between 40 and 80 1/10 mm. A person skilled in the art can modulate the penetrability of the clear binder usable in the invention, in particular by judiciously choosing the weight ratio [structuring agent / plasticizing agent] in the composition of the clear binder base. Indeed, it is known that an increase in this ratio makes it possible to reduce the penetrability at 25 ° C. The clear binder bases used in the invention can be prepared, for example, according to the following process comprising the steps of: (i) mixing of the plasticizing agent, for example DAO oil, and heating to a temperature of between 140-200 ° C., for example from 10 minutes to 30 minutes, (ii) addition of the structuring agent, by example the hydrocarbon resin, mixing and heating at a temperature between 140-200 ° C, for example from 30 minutes to 2 hours, (iii) addition of the polymer or polymers, for example SB S, mixing and heating at a temperature between 140-200 ° C, for example, from 90 minutes to 3 hours, preferably from 90 minutes to 2 hours 30, (iv) optional addition of a dope of adhesiveness, mixing and heating to a temperature between 140- 200 ° C, for example, from 5 minutes to 20 minutes. The order of steps (i) to (iv) can be changed. According to one embodiment of the invention, the cores of the clear binder granules further comprise at least one coloring agent as described above, such as for example a pigment. In these embodiments, the anti-caking agent and / or the coloring agent will be chosen by a person skilled in the art as a function of the color of the desired clear binder. ICG70142 EN text deposit 17 The pitch According to the French dictionary, "pitch" is understood to mean a residue from the distillation of petroleum tar, petroleum, coal, wood or other organic molecules. The invention relates here to petroleum distillation residues, also called "petroleum pitch". For the purposes of the invention, the terms "pitch", "oil pitch" and "deasphalting pitch" will be used independently of one another. The pitches can be obtained by conventional refinery manufacturing processes. The manufacturing process corresponds to the succession of atmospheric distillation and vacuum distillation. Initially, the crude oil is subjected to distillation at atmospheric pressure, which leads to the production of a gas phase, various distillates and an atmospheric distillate residue. Then, the residue from atmospheric distillation is itself subjected to distillation under reduced pressure, called vacuum distillation, which makes it possible to separate a heavy diesel fuel, various cuts of distillais and a residue of vacuum distillation. This vacuum distillation residue contains “petroleum pitch” in varying concentrations. You can get the "petroleum pitch" by two methods: the era process: The vacuum distillation residue is subjected to a desalphating operation by the addition of an appropriate solvent, such as propane, which thus makes it possible to precipitate the pitch and to separate it from light fractions such as deapphalted oil. 2 nd method: The vacuum distillation residue is subjected to solvent extraction, and more specifically to furfural. This heterocyclic aldehyde has the particularity of selectively solubilizing aromatic and polycyclic compounds. This process thus allows the aromatic extracts to be removed and the "oil pitch" to be recovered. According to one embodiment, the pitch is an oxidized pitch. Preferably, the oxidized pitch according to the invention is obtained by oxidation of a mixture comprising pitch and a diluent, such as a light gasoline, also called "fluxing agent" subjected to an oxidation operation in a blowing tower in presence of a catalyst, at a fixed temperature and at a given pressure. ICG70142 EN text deposit 18 For example, oxidized pitches can be manufactured in a blowing unit, by passing a flow of air and / or oxygen through a starting pitch. This operation can be carried out in the presence of an oxidation catalyst, for example phosphoric acid. Generally, the oxidation is carried out at high temperatures, of the order of 200 to 300 ° C, for relatively long periods typically between 30 minutes and 2 hours, continuously or in batches. The duration and the temperature of oxidation are adjusted according to the properties targeted for the oxidized pitch and according to the quality of the starting pitch. The mechanical qualities of pitches are generally assessed by determining a series of mechanical characteristics by standardized tests, the most widely used of which are the needle penetration expressed in 1/10 mm and the softening point determined by the ball and ring test. , also called ball and ring softening temperature (TBA). According to one embodiment of the invention, the pitch has a needle penetration at 25 ° C from 0 to 20 1/10 mm, preferably from 0 to 15 1/10 mm, more preferably from 0 to 10 1 / 10 mm, it being understood that the penetrability is measured according to standard EN 1426. According to one embodiment of the invention, the pitch has a softening point between 115 ° C and 175 ° C. Among examples of pitches used in the invention, there are pitches having respectively a softening point between 115 ° C and 125 ° C, between 135 and 145 ° C or even between 165 and 175 ° C. The plasticizer By “plasticizing agent” is meant, within the meaning of the invention, a chemical constituent making it possible to thin and reduce the viscosity and the modulus of the binder obtained. In one embodiment of the invention, the plasticizing agent is chosen from oils of petroleum origin, oils of vegetable origin and their mixture. In a preferred embodiment of the invention, the oils of vegetable origin are chosen from rapeseed, sunflower, soybean, linseed, olive, palm, castor, wood, corn, squash, grapeseed, jojoba, sesame, walnut, hazelnut, almond, shea, macadamia, cotton, alfalfa, rye, safflower, peanut, coconut and copra, and mixtures thereof. Preferably, the oils of vegetable origin are chosen from rapeseed, sunflower, linseed, coconut, soybean oils and their mixtures. ICG70142 EN text deposit 19 In a preferred embodiment of the invention, the oils of petroleum origin are chosen from aromatic oils or oils of synthetic origin. Preferably, the aromatic oils comprise aromatic extracts of petroleum residues, obtained by extraction or dearomatization of residues from distillation of petroleum fractions. More preferably, the aromatic oils have a content of aromatic compounds between 30 and 95% by weight, advantageously between 50 and 90% by weight, more advantageously between 60 and 85% by weight (SARA Saturated / Aromatic / Resins / method) Asphaltenes). More preferably, the aromatic oils have a content of saturated compounds of between 1 and 20% by weight, advantageously between 3 and 15% by weight, more advantageously between 5 and 10% by weight (SARA Saturated / Aromatic / Resins / method). Asphaltenes). More preferably, the aromatic oils have a content of resin compounds of between 1 and 10% by weight, advantageously between 3 and 5% by weight, (SARA method: Saturated / Aromatic / Resins / Asphaltenes). In a preferred embodiment of the invention, the oils of synthetic origin are obtained from deasphalting cuts for distillation under reduced pressure (residue under vacuum, RSV) of crude oil (hereinafter referred to as "CAD oil"). In particular, in a preferred embodiment, the plasticizer consists only of a CAD oil. The contents of paraffinic, naphthenic and aromatic compounds mentioned in the present application are determined according to standard ASTM D2140, in% by weight relative to the weight of the oil. In a specific embodiment, the plasticizing agent is an oil, for example a DAO oil, containing a total content of paraffinic compounds of at least 50% by weight, preferably at least 60% by weight, for example between 50% and 90%, preferably between 60% and 90%, more preferably between 50% and 80% and in particular between 55% and 70% or in particular between 60% and 75%. ICG70142 EN text deposit 20 In a more specific embodiment, the plasticizing agent is an oil, for example a DAO oil, further containing a total content of naphthenic compounds which does not exceed 25%, for example between 5% and 25%, and in particular between 10% and 25%. In a more specific embodiment, the plasticizing agent is an oil, for example a DAO oil, further containing a total aromatic content which does not exceed 25%, for example between 5% and 25%, and particular between 8% and 18%. In a particularly preferred embodiment, the plasticizing agent is an oil, for example a DAO oil, comprising the respective contents: (i) a total content of paraffinic compounds of between 50% and 90%; (ii) a total content of naphthenic compounds of between 5% and 25%, for example between 15% and 25%; and (iii) a total content of aromatic compounds of between 5% and 25%, for example between 10% and 15%. In a more particularly preferred embodiment, the plasticizing agent is an oil, for example a CAD oil, comprising the respective contents: (i) a total content of paraffinic compounds of between 60% and 75%; (ii) a total content of naphthenic compounds of between 5% and 25%, for example between 15% and 25%; and (iii) a total content of aromatic compounds of between 5% and 25%, for example between 10% and 15%. Oils meeting the above characteristics and which can be used for the preparation of the clear binder according to the invention are obtained by the processes for deasphalting of residues under vacuum (RSV) originating from the refining of petroleum, for example by deasphalting using 'a C3 to C6 solvent, preferably propane. These deasphalting processes are well known to those skilled in the art and are described for example in Lee et al 2014, Fuel Processing Technology 119: 204-210: The residues resulting from vacuum distillation (RSV) are separated according to their molecular weight. in the presence of solvent C3 to C6 (for example propane). The oil called DAO (“deasphalted oil”) thus obtained is rich in paraffin, has a very low asphaltene content, has an evaporation temperature between 440 ° C and 750 ° C, and an API gravity much higher than that vacuum residues. The respective levels of paraffinic, naphthenic and aromatic compounds depend to some extent on the nature of the crude oil that produces the CAD oil and the refining process used. A person skilled in the art knows how to determine the respective contents ICG70142 FR text deposit 21 paraffinic, naphthenic and aromatic compounds of a CAD oil for example using the SARA fractionation method also described in Fee et al 2014, Fuel Processing Technology 119: 204-210 and thus select the oil DAO suitable for the preparation of the clear binder according to the invention. In one embodiment, the amount of plasticizer used in the process for preparing the clear binder base is from 40% to 80%, preferably from 45% to 70% by weight relative to the total weight of clear binder base. The structuring agent By "structuring agent" is meant any chemical constituent conferring mechanical properties and satisfactory cohesiveness to said binder. The structuring agent used in the context of the invention is a resin, preferably chosen from resins of hydrocarbon petroleum origin, for example resulting from the copolymerization of aromatic, aliphatic, cyclopentadienic petroleum fractions, taken alone or as a mixture, preferably from aromatic petroleum couples. For example, it may be a polycycloaliphatic thermoplastic resin, for example of the hydrogenated cyclopentadiene homopolymer type, with a low molecular weight. More particularly, the hydrocarbon resin of the cyclopentane type has a softening point (or ball-ring temperature, TB A, according to standard NF T 66-008) greater than 125 ° C, and a Gardner color index (according to standard NF T 20-030) equal to a maximum of 1. Other examples of resins which can be used as a structuring agent include, without being limiting, resins of vegetable origin obtained from plants and / or plants. They can be called harvest, that is to say harvested from the living plant. They can be used as such, we then speak of natural resins or be chemically transformed, we then speak of modified natural resins. Among the crop resins are addictive resins, dammar, natural rosins, modified rosins, rosin esters and metallic resins. These can be taken alone or as a mixture. Among the natural rosins, mention may be made of gemstones and wood rosins, in particular pine, and / or tall oil. These natural rosins can be taken alone or as a mixture. Among the modified rosins, mention may be made of hydrogenated rosins, disproportionated rosins, polymerized rosins and / or maleized rosins. These modified natural rosins can be taken alone or as a mixture, and undergo one or more disproportionation, polymerization and / or maleization treatments. ICG70142 EN text deposit 22 Among the rosin esters, mention may be made of methyl esters of natural rosins, methyl esters of hydrogenated rosins, glycerol esters of natural rosins, glycerol esters of hydrogenated rosins, glycerol esters of disproportionated rosins, esters of glycerol and polymerized rosins, esters of glycerol and maleized rosins, esters of pentaerythritol and natural rosins and esters of pentaerythritol and hydrogenated rosins. These rosin esters can be taken alone or as a mixture and come from rosins having undergone one or more disproportionation, polymerization and / or maleization treatments. The esters of pentaerythritol and natural rosins and the esters of pentaerythritol and hydrogenated rosins are the preferred rosin esters. Among the metallic resins, mention may be made of metallic carboxylates, for example of Ca, Zn, Mg, Ba, Pb, Co, obtained from natural rosins or modified rosins. Preference is given to calcium resins, zinc resins, mixed calcium / zinc resins, taken alone or as a mixture. The weight ratio between the structuring agent and the plasticizing agent used for the preparation of the clear binder is generally understood to be 0.3 to 1.5, for example 0.5 to 1. In a specific embodiment, the amount of structuring agent used in the process for the preparation of the clear binder base is from 25 to 50% by weight relative to the total weight of the clear binder base. The polymer The polymer used in the first composition is a copolymer based on conjugated diene units and monovinyl aromatic hydrocarbon units. Fe conjugated diene is preferably chosen from those comprising from 4 to 8 carbon atoms per monomer, for example butadiene, 2-methyl-1,3-butadiene (isoprene), 2,3-dimethyl-1,3, butadiene, 1,3-pentadiene and 1,2-hexadiene, chloroprene, carboxylated butadiene, carboxylated isoprene, in particular butadiene and isoprene, and mixtures thereof. The aromatic monovinyl hydrocarbon is preferably chosen from styrene, methyl styrene, p-methyl styrene, p-tert-butylstyrene, 2,3 dimethylstyrene, Pa-methyl styrene, vinyl naphthalene, vinyl toluene, vinyl xylene, and the like or mixtures thereof, in particular styrene. More particularly, the polymer consists of one or more copolymers chosen from block copolymers of styrene and butadiene, styrene and isoprene, styrene and chloroprene, styrene and butadiene carboxylate or even styrene and isoprene carboxylated. A preferred copolymer is a copolymer based on butadiene units and ICG70142 FR text deposit 23 styrene such as the styrene / butadiene block copolymer SB or the styrene / butadiene / styrene block copolymer SB S. The copolymer of styrene and conjugated diene, in particular the copolymer of styrene and butadiene, advantageously has a weight content of styrene ranging from 5 to 50%, preferably from 20 to 50%. The copolymer of styrene and conjugated diene, in particular the copolymer of styrene and butadiene, advantageously has a weight content of butadiene (1-2 and 1-4) ranging from 50 to 95%. The copolymer of styrene and conjugated diene, in particular the copolymer of styrene and butadiene, advantageously has a content by weight of 1-2 butadiene ranging from 5 to 70%, preferably from 5 to 50%. The 1-2 butadiene units are the units which result from the polymerization via the 1-2 addition of the butadiene units. The weight-average molecular mass of the copolymer of styrene and of conjugated diene, and in particular that of the copolymer of styrene and of butadiene, can be comprised, for example, between 10,000 and 500,000, preferably between 50,000 and 200,000 and more preferably from 50,000 to 150,000 daltons. In a specific embodiment, the total quantity of polymer used in the process of the invention is from 0.5 to 20% by mass, preferably from 1 to 10%, preferably from 1 to 7%, per example from 2% to 5% relative to the total mass of bitumen base, or of clear binder. In another specific embodiment, the total amount of polymer used in the process of the invention is from 20% to 50% by mass, relative to the total mass of bitumen base, or relative to the total mass clear binder base. In this case, the first composition is called mother solution of bitumen / polymer composition or mother solution of clear binder / polymer composition. It is intended to be transported and stored in concentrated form, then diluted with the desired quantity of bitumen base or clear binder base just before its use as a road binder or as a coating binder. According to the invention, it is possible to form granules of bitumen or clear binder stock solution, so as to facilitate their transport and storage as well as their handling at a high ambient temperature. According to a variant of the invention, the polymer is chosen from micronized polymers. Preferably, according to this variant, the polymer has particles of diameter ranging from 250 to 1000 μιη, preferably of diameter ranging from 400 to 600 μιη. ICG70142 EN text deposit 24 Compatibilizer Preferably, the compatibilizing agent is chosen from waxes, for example animal waxes, vegetable waxes, mineral waxes and their mixtures. Animal and vegetable waxes are mainly composed of mixtures of fatty acid derivatives (fatty acid esters) while mineral waxes are paraffinic derivatives. Adhesive dopes To improve the reciprocal affinity between the binder and the aggregates and to ensure their durability, adhesiveness dopes can also be used in the first composition, in mixture with the other components, in particular the clear binder, or the bitumen base or the pitch. They are, for example, nitrogen-containing surfactant compounds derived from fatty acids (amines, polyamines, alkyl-polymane, etc.). When added to the first composition, the adhesive dopes generally represent between 0.05% and 0.5% by weight relative to the weight of clear binder or bitumen base or pitch. For example, in a specific embodiment, 0.05% to 0.5% of amine will be added, preferably 0.1% to 0.3% of amine relative to the total basic mass of clear binder or base bitumen or pitch. Coloring agents The clear synthetic binder can also comprise one or more coloring agents, such as mineral pigments or organic dyes. The pigments are selected according to the shade, the desired color for the coating. For example, metal oxides such as iron oxides, chromium oxides, cobalt oxides, titanium oxides will be used to obtain the colors red, yellow, gray, blue green or white. The pigments can be added, either in the clear binder or in the mix (in admixture with the aggregates for example) or in an emulsion of the clear binder. The chemical additive The bitumen base, the pitch or the clear binder can also comprise at least one chemical additive chosen from: an organic compound, a paraffin, a polyphosphoric acid and their mixtures. In particular, when the solid material comprises at least one chemical additive, this is in an amount suitable so that its penetrability is preferably 5 to 50 l / 10mm and / or that the ball and ring softening temperature (TBA) is, preferably, superior or ICG70142 FR text deposit 25 equal to 60 ° C, it being understood that the penetrability is measured at 25 ° C according to standard EN 1426 and the TBA according to standard EN 1427. According to a first embodiment of the invention, the chemical additive is an organic compound. Advantageously, the organic compound has a molar mass less than or equal to 2000 gmol ' 1 , preferably a molar mass less than or equal to 1000 gmol' 1 . In this first embodiment, according to a first variant, the organic compound is a compound of general formula (I): Arl-R-Ar2 (I), in which: • Arl and Ar2 independently of one another represent a benzene ring or a system of condensed aromatic rings of 6 to 20 carbon atoms, substituted by at least one hydroxyl group, and • R represents an optionally substituted divalent radical, of which the main chain comprises from 6 to 20 carbon atoms and at least one group chosen from the amide, ester, hydrazide, urea, carbamate, anhydride functions. Preferably, Arl and / or Ar2 are substituted by at least one alkyl group of 1 to 10 carbon atoms, advantageously in one or more positions ortho with respect to the hydroxyl group (s), more preferably Arl and Ar2 are 3,5-dialkyl-4hydroxyphenyl groups, advantageously 3,5-di - / < / 7-butyl-4-hydroxyphenyl groups. Preferably, R is in the para position with respect to a hydroxyl group of Arl and / or Ar2. Advantageously, the compound of formula (I) is 2 ’, 3-bis [(3- [3, 5-di-fe / 7-butyl-4hydroxyphenyl] propionyl)] propionohydrazide. According to a second variant of this first embodiment, the organic compound is a compound of general formula (II): R- (NH) „CONH- (X) m -NHCO (NH)„ - R '(II), in which, -the groups R 'and R ”, identical or different, represent a saturated or unsaturated, linear, branched or cyclic hydrocarbon chain, comprising from 1 to 22 carbon atoms, and optionally comprising heteroatoms such as N, O, S, C5-C24 hydrocarbon rings and / or C4-C24 hydrocarbon heterocycles comprising one or more heteroatoms such as N, O, S, and R ”may be H; the group X represents a hydrocarbon chain, saturated or unsaturated, linear, cyclic or branched, comprising from 1 to 22 carbon atoms, optionally substituted, and optionally comprising heteroatoms, such as N, O, S, C5 hydrocarbon rings -C24 and / or C4-C24 hydrocarbon heterocycles comprising one or more heteroatoms such as N, O, S; ICG70142 FR text deposit - n and m are integers having a value of 0 or 1 independently of each other. According to this variant, when the integer has a value of 0, then the groups R (NH) nCONH and NHCO (NH) n -R 'are covalently linked by a hydrazide bond CONHNHCO. The group R, or the group R ′, then comprises at least one group chosen from: a hydrocarbon chain of at least 4 carbon atoms, an aliphatic ring of 3 to 8 atoms, an aliphatic condensed polycyclic system, partially aromatic or entirely aromatic, each cycle comprising 5 or 6 atoms. Still according to this variant, when the integer has a value of 1, then the group R, the group R 'and / or the group X, comprises at least one group chosen from: a hydrocarbon chain of at least 4 carbon atoms , an aliphatic ring of 3 to 8 atoms, an aliphatic condensed polycyclic system, partially aromatic or entirely aromatic, each cycle comprising 5 or 6 atoms. Preferably, the group R and / or R ′ comprises an aliphatic hydrocarbon chain of 4 to 22 carbon atoms, in particular, chosen from the groups C4H9, C5H11, C9H19, C11H23, C12H25, C17H35, C18H37, C21H43, C22H45. Preferably, the group X represents a linear, saturated hydrocarbon chain comprising from 1 to 22 carbon atoms, advantageously X represents a linear, saturated hydrocarbon chain comprising from 1 to 12 carbon atoms, even better from 1 to 4 carbon atoms. Preferably, the group X is chosen from the groups C2H4, C 3 H 6 . Preferably, the group X can also be a cyclohexyl group or a phenyl group, the radicals R- (NH) n CONH- and NHCO (NH) n -R'- can then be in the ortho, meta or para position. Furthermore, the radicals R- (NH) n CONH- and NHCO (NH) n -R'may be in the cis or trans position with respect to each other. In addition, when the radical X is cyclic, this ring can be substituted by other groups than the two main groups R- (NH) „CONH- and -NHCO (NH)„ - R '. Preferably, the group X comprises two cycles of 6 carbons linked by a CH 2 group, these cycles being aliphatic or aromatic. In this case, the group X is a group comprising two aliphatic rings linked by an optionally substituted CH 2 group, for example: Advantageously, according to this variant, the organic compound is a compound of general formula (II) chosen from hydrazide derivatives such as the compounds C5H11-CONHNHCO-C5H11, C9H19-CONH-NHCO-C9H19, C11H23-CONH-NHCO-C11H23, Ci 7 H 35 -CONHNHCO-Ci 7 H 35 , or C21H43-CONH-NHCO-C21H43; diamides such as N, N'3065464 ICG70142 FR ethyleneedi (laurylamide) text deposit of formula C11H23-CONH-CH2-CH2-NHCO-C11H31, N, N'ethylenedi (myristylamide) of formula C13H27-CONH-CH2-CH2-NHCO-C13H27, N, N ' ethylenedi (palmitamide) of formula C15H31-CONH-CH2-CH2-NHCO-C15H31, N, N'ethylenedi (stearamide) of formula C17H35-CONH-CH2-CH2-NHCO-C17H35; - monoamides such as laurylamide of formula C11H23-CONH2, myristylamide of formula C13H27-CONH2, palmitamide of formula C15H31-CONH2, stearamide of formula C17H35-CONH2; . ureide derivatives such as 4,4'-bis (dodecylaminocarbonylamino) diphenylmethane of formula CnHîs-NHCONH-CeH ^ CHj-CeH ^ NHCONH-Cnïc. According to a third variant of this embodiment, the organic compound is a compound of formula (III): (R-NHCO) X -Z- (NHCO-R ') y (III), in which, -R and R ’, identical or different, contain a saturated or unsaturated, linear, branched or cyclic hydrocarbon chain comprising from 1 to 22 carbon atoms, optionally substituted, and optionally comprising heteroatoms, rings and / or heterocycles, - Z represents a tri-functionalized group chosen from the following groups: - x and y are different integers with values varying from 0 to 3 and such that x + y = 3. Preferably, when x is equal to 0 and Z represents Z 2 , the compound of formula (III) is N2, N4, N6-tridecylmelamine having the following formula with R 'representing the group C 9 Hi 9 : HN H NH ICG70142 EN text deposit 28 Other preferred compounds corresponding to formula (III) are such that x is equal to 0, Z represents Z 2 and R ′ represents a saturated, linear hydrocarbon chain of 1 to 22 carbon atoms, preferably of 2 to 18 carbon atoms, preferably 5 to 12 carbon atoms. Other preferred compounds corresponding to formula (III) are such that: y is equal to 0 and Z 5 represents Zi, the compounds then have the formula: with R chosen from the following groups, taken alone or as a mixture: '1 II WW WW WW WW WW Λ (x ô (7 Other preferred compounds corresponding to formula (III) are such that: y is equal to 0, Z 10 represents Zi and R represents a saturated, linear hydrocarbon chain of 1 to 22 carbon atoms, preferably of 8 to 12 carbon atoms. According to a fourth variant of this embodiment, the organic compound is a reaction product of at least one C3-C12 polyol and at least one C2-C12 aldehyde. Among the polyols which can be used, mention may be made of sorbitol, xylitol, mannitol and / or ribitol. Preferably, the polyol is sorbitol. Advantageously, according to this variant, the organic compound is a compound which comprises at least one function of general formula (IV): (IV) With: - x is an integer, -R is chosen from a C1-Cl1 alkyl, alkenyl, aryl or aralkyl radical, optionally substituted by one or more halogen atoms, one or more C1-C6 alkoxy groups. ICG70142 EN text deposit 29 The organic compound is advantageously a derivative of sorbitol. By "sorbitol derivative" is meant any reaction product obtained from sorbitol. In particular, any reaction product obtained by reacting an aldehyde with D-sorbitol. This condensation reaction produces sorbitol acetals, which are derivatives of sorbitol. 1,3: 2,4Di-O-benzylidene-D-sorbitol is obtained by reacting 1 mole of D-sorbitol and 2 moles of benzaldehyde and has the formula: The sorbitol derivatives can thus be all the condensation products of aldehydes, in particular aromatic aldehydes with sorbitol. We will then obtain sorbitol derivatives of general formula: where Ari and Ar 2 are optionally substituted aromatic rings. Among the sorbitol derivatives, other than 1,3: 2,4-Di-O-benzylidene-D-sorbitol, there can be found, for example, 1,3: 2,4: 5,6-tri-O-benzylidene- D-sorbitol, 2,4-mono-O-benzylidene D-sorbitol, l, 3: 2,4-bis (p-methylbenzylidene) sorbitol, l: 3: 2,4-bis (3,4-dimethylbenzylidene) sorbitol, 1,3: 2,4-bis (p-ethylbenzylidene) sorbitol, 1,3: 2,4-bis (p-propylbenzylidene) sorbitol, 1,3: 2,4-bis (p-butylbenzylidene) sorbitol, l, 3: 2,4-bis (p-ethoxylbenzylidene) sorbitol, 1,3: 2,4bis (p-chlorobenzylidene) sorbitol, l: 3: 2,4-bis (p-bromobenzylidene) sorbitol, 1,3: 2,4-Di-Omethylbenzylidene-D-sorbitol, 1,3: 2,4-Di-O-dimethylbenzylidene-D-sorbitol, 1,3: 2,4-Di-O (4-methylbenzylidene) -D-sorbitol , 1,3: 2,4-Di-O- (4,3-dimethylbenzylidene) -D-sorbitol. Preferably, according to this variant, the organic compound is 1,3: 2,4-Di-O-benzylidene-Dsorbitol. According to a fifth variant of this embodiment, the organic compound is a compound of general formula (V): R ”- (COOH) Z (V), in which R” represents a linear or branched, saturated or unsaturated chain comprising from 4 to 68 carbon atoms, preferably from 4 to 54 carbon atoms, more preferably from 4 to 36 carbon atoms and z is an integer varying from 2 to 4. ICG70142 FR text deposit Preferably, the group R "is preferably a saturated linear chain of formula C w H 2w with w an integer varying from 4 to 22, preferably from 4 to 12. According to this variant of the invention, the organic compounds corresponding to formula (V) can be diacids (z = 2), triacids (z = 3) or tetracids (z = 4). The preferred organic compounds according to this variant are diacids with z = 2. Preferably, according to this variant, the diacids have the general formula HOOCCwH 2w -COOH with w an integer varying from 4 to 22, preferably from 4 to 12 and where z = 2 and R = Advantageously, according to this variant, the organic compound is a diacid chosen from adipic acid or 1,6-hexanedioic acid with w = 4, pimelic acid or 1,7heptanedioic acid with w = 5, suberic acid or acid 1,8-octanedioic with w = 6, azelaic acid or 1,9-nonanedioic acid with w = 7, sebacic acid or 1,10decanedioic acid with w = 8, undecanedioic acid with w = 9, l 1,2-dodecanedioic acid with w = 10 or tetradecanedioic acid with w = 12. Advantageously, the diacid is sebacic acid. The diacids may also be dimer diacids of unsaturated fatty acid (s), that is to say dimers formed from at least one unsaturated fatty acid, for example from a single unsaturated fatty acid or from two different unsaturated fatty acids. The diacid dimers of unsaturated fatty acid (s) are conventionally obtained by intermolecular dimerization reaction of at least one unsaturated fatty acid (reaction of Diels Aider for example). Preferably, a single type of unsaturated fatty acid is dimerized. They derive in particular from the dimerization of an unsaturated fatty acid in particular in Cx to C34, in particular in C12 to C22, in particular in Ci6 to C20, and more particularly in Cis. A preferred fatty acid dimer is obtained by dimerization of linoleic acid, which can then be partially or completely hydrogenated. Another preferred fatty acid dimer has the formula HOOC- (CH 2 ) 7CH = CH- (CH 2 ) 7-COOH. Another preferred fatty acid dimer is obtained by dimerization of methyl linoleate. Similarly, fatty acid triacids and fatty acid tetracids can be found, obtained respectively by trimerization and tetramerization of at least one fatty acid. According to a sixth variant of this embodiment, the organic compound is a compound of general formula (VI): Y (VI) ICG70142 EN text deposit 31 in which, - the groups Y and Y 'represent, independently of one another, an atom or group chosen from: H, - (CH 2 ) q-CH 3 , - (CH 2 ) q-NH 2 , - (CH 2 ) q-OH, - (CH 2 ) q-COOH or - (CH 2 ) q -NH- (CH 2 ) q - N, with q an integer varying from 2 to 18, preferably from 2 to 10, preferably from 2 to 4 and p an integer greater than or equal to 2, preferably having a value of 2 or 3. Among the preferred organic compounds corresponding to formula (VI), mention may be made of the following compounds: o HN NH O nh 2 o O NH Preferably, according to this variant, the organic compound of general formula (VI) is: ΓΛ HN. .NOT nh 2 O According to a seventh variant of this embodiment, the organic compound is a compound of general formula (VII): R-NH-CO-CO-NH-R '(VII) in which, R and R', identical or different, represent a saturated or unsaturated hydrocarbon chain, linear, branched or cyclic, comprising from 1 to 22 carbon atoms, preferably from 8 to 12 carbon atoms, optionally substituted, and optionally comprising heteroatoms, rings and / or heterocycles. ICG70142 EN text deposit 32 According to another embodiment of the invention, the chemical additive is a paraffin. The paraffins have chain lengths of 30 to 120 carbon atoms (C30 to C120). The paraffins are advantageously chosen from polyalkylenes. Preferably, according to the invention, polymethylene paraffins and polyethylene paraffins will be used. These paraffins can be of petroleum origin or come from the chemical industry. Advantageously, the paraffins used are synthetic paraffins resulting from the conversion of biomass and / or natural gas. Preferably, these paraffins contain a large proportion of so-called “normal” paraffins, that is to say straight, straight chain, unbranched paraffins (saturated hydrocarbons). Thus, the paraffins can comprise from 50 to 100% of normal paraffins and from 0 to 50% of isoparaffins and / or branched paraffins. More preferably, the paraffins comprise from 85 to 95% of normal paraffins and from 5 to 15% of isoparaffins and / or branched paraffins. Advantageously, the paraffins comprise from 50 to 100% of normal paraffins and from 0 to 50% of isoparaffins. Even more advantageously, the paraffins comprise from 85 to 95% of normal paraffins and from 5 to 15% of isoparaffins. Preferably, the paraffins are polymethylene paraffins. More particularly, the paraffins are synthetic paraffins of polymethylene, for example paraffins resulting from the conversion of synthesis gas by the Fischer-Tropsch process. In the Fischer-Tropsch process, paraffins are obtained by reacting hydrogen with carbon monoxide on a metal catalyst. Fischer-Tropsch synthesis methods are described for example in the publications EP 1 432 778, EP 1 328 607 or EP 0 199 475. According to another embodiment of the invention, the chemical additive is a polyphosphoric acid. The polyphosphoric acids (PPA) which can be used in the invention are described in WO 97/14753. These are compounds of the raw formula PqHrOs in which q, r and s are positive numbers such as: q> 2 and in particular q goes from 3 to 20 or more and that 5q + r-2s = 0. In particular, said polyphosphoric acids can be linear compounds of crude formula P q H ( q + 2) O (3q + i) corresponding to the structural formula: Where q has the definition given above. They can also be products of two-dimensional or three-dimensional structure. All these polyphosphoric acids can be considered as polycondensation products by heating the aqueous metaphosphoric acid. It will not depart from the scope of the invention to combine several different chemical additives such as different organic compounds of formula (I), (II), (III), (V), (VI) and (VII), ICG70142 FR text deposit 33 the reaction products of at least one C3-C12 polyol and at least one C2-C12 aldehyde, in particular those comprising a group of formula (IV), and / or different paraffins and / or different polyphosphoric acids in the material usable as road binder or as waterproofing binder. Advantageously, when a chemical additive is used in the material which can be used as a road binder or as a sealing binder, it is chosen from the compounds of formula (I), the compounds of formula (II), the compounds of formula (V) and mixtures of these compounds. Even more advantageously, when a chemical additive is used in the material which can be used as a road binder or as a sealing binder, it is chosen from: - 2 ’, 3-bis [(3- [3, 5-di - / < / 7-butyl-4-hydroxyphenyl] propionyl)] propionohydrazide, - sebacic acid, - hydrazide derivatives such as: C 5 Hn-CONH-NHCO-C 5 Hn, C 9 Hi 9 -CONH-NHCOC 9 Hi 9 , CiiH 2 3-CONH-NHCO-CiiH 23 , Ci 7 H 35 -CONH-NHCO -Ci 7 H 35 , or C 2 iH 43 -CONHNHCO-C 2 iH 43 ; - diamides such as N, N'-ethylenedi (laurylamide) of formula CnH 23 -CONH-CH 2 CH 2 -NHCO-ChH 3 i, N, N'-ethylenedi (myristylamide) of formula Ci 3 H 2 7 -CONH-CH 2 -CH 2 NHCO-Ci 3 H 27 , the N, N'-ethylenedi (palmitamide) of formula Ci5H 3 i-CONH-CH 2 -CH 2 -NHCOCi 5 H 3 i, leN, N'- ethylenedi (stearamide) of formula Ci7H 35 -CONH-CH 2 -CH 2 -NHCO-Ci7H 3 5; - monoamides such as laurylamide of formula CnH 23 -CONH 2 , myristylamide of formula Ci 3 H 2 7-CONH 2 , palmitamide of formula Ci5H 3 i-CONH 2 , stearamide of formula Ci7H 35 -CONH 2 , and mixtures of these compounds. More preferably, when a chemical additive is used in the material which can be used as a road binder or as a sealing binder, it is chosen from: - 2 ’, 3-bis [(3- [3, 5-di - / < / 7-butyl-4-hydroxyphenyl] propionyl)] propionohydrazide, - sebacic acid, and mixtures of these compounds. According to another preferred embodiment, when a chemical additive is used in the material which can be used as a road binder or as a sealing binder, it is chosen from: - diamides, such as N, N'-ethylenedi (laurylamide) of formula CnH 23 -CONH-CH 2 CH 2 -NHCO-ChH 3 i, N, N'-ethylenedi (myristylamide) of formula Ci 3 H 2 7-CONH-CH 2 -CH 2 NHCO-Ci 3 H 27 , the N, N'-ethylenedi (palmitamide) of formula Ci5H 3 i-CONH-CH 2 -CH 2 -NHCOCi 5 H 3 i, leN, N ' -ethylenedi (stearamide) of formula Ci7H 35 -CONH-CH 2 -CH 2 -NHCO-Ci7H 3 5 - sebacic acid, and mixtures of these compounds. According to one embodiment of the invention, the first composition, comprising a bitumen base, of which the core of the granules is composed, comprises from 0.1% to 10% by mass, ICG70142 EN text deposit 34 preferably from 0.5% to 5% by mass, more preferably from 0.5% to 2.5% by mass of chemical additive relative to the total mass of the first composition. Olefinic polymer admixture According to one embodiment of the invention, the first composition can also comprise at least one olefinic polymeric adjuvant. The olefinic polymeric adjuvant is preferably selected from the group consisting of (a) ethylene / glycidyl (meth) acrylate copolymers; (b) the ethylene / monomer A / monomer B terpolymers and (c) the copolymers resulting from the grafting of a monomer B onto a polymer substrate. (a) the ethylene / glycidyl (meth) acrylate copolymers are advantageously chosen from random or block, preferably statistical, copolymers of ethylene and of a monomer chosen from glycidyl acrylate and glycidyl methacrylate, comprising from 50% to 99.7% by mass, preferably from 60% to 95% by mass, more preferably 60% to 90% by mass of ethylene. (b) The terpolymers are advantageously chosen from random or block, preferably random, terpolymers of ethylene, of a monomer A and of a monomer B. Fe monomer A is chosen from vinyl acetate and C1 to C6 alkyl acrylates or methacrylates. Fe monomer B is chosen from glycidyl acrylate and glycidyl methacrylate. The ethylene / monomer A / monomer B terpolymers comprise from 0.5% to 40% by mass, preferably from 5% to 35% by mass, more preferably from 10% to 30% by mass of units derived from monomer A and, 0.5% to 15% by mass, preferably 2.5% to 15% by mass of units from monomer B, the remainder being formed from units from ethylene. (c) The copolymers result from the grafting of a monomer B chosen from glycidyl acrylate and glycidyl methacrylate, on a polymer substrate. The polymer substrate consists of a polymer chosen from polyethylenes, in particular low density polyethylenes, polypropylenes, random or block copolymers, preferably statistical, of ethylene and vinyl acetate and random or block copolymers, preferably statistical , ethylene and C1 to C6 alkyl acrylate or methacrylate, comprising from 40% to 99.7% by mass, preferably from 50% to 99% by mass of ethylene. Said graft copolymers comprise from 0.5% to 15% by mass, preferably from 2.5% to 15% by mass of grafted units derived from monomer B. ICG70142 EN text deposit 35 Advantageously, the olefinic polymeric adjuvant is chosen from random terpolymers of ethylene (b), of a monomer A chosen from acrylates or methacrylates of C1-C6 alkyl and of a monomer B chosen from acrylate of glycidyl and glycidyl methacrylate, comprising from 0.5% to 40% by mass, preferably from 5% to 35% by mass, more preferably from 10% to 30% by mass of units derived from monomer A and, from 0, 5% to 15% by mass, preferably from 2.5% to 15% by mass of units originating from monomer B, the remainder being formed from units originating from ethylene. According to one embodiment of the invention, the first composition, comprising the bitumen base, of which the core of the granules is composed, comprises from 0.05% to 15% by mass, preferably from 0.1% to 10% by weight. mass, more preferably from 0.5% to 6% by mass of the olefinic polymeric adjuvant, relative to the total mass of the first composition. According to one embodiment of the invention, the first composition may also comprise other known additives or other known elastomers for bitumen such as the copolymers SB (block copolymer of styrene and butadiene), SB S (copolymer with styrene-butadiene-styrene blocks), SIS (styrene-isoprene-styrene), SBS * (styrene-butadiene-styrene block copolymer in star), SBR (styrene-b-butadiene-rubber), EPDM (modified ethylene propylene diene). These elastomers can also be crosslinked according to any known process, for example with sulfur. Mention may also be made of the elastomers produced from styrene monomers and butadiene monomers allowing crosslinking without crosslinking agent as described in documents WO2007 / 058994, WO2008 / 137394 and by the applicant in patent application WO11 / 013073. According to a particular preferred embodiment, the first composition comprises a combination of the chemical additive of formula (II) and the olefinic polymeric adjuvant described above. We prefer the combination in which the chemical additive is of formula (II) where m = 0, more preferably where m = 0 and n = 0. The combination in which the olefinic polymer adjuvant is chosen from the terpolymers (b) ethylene / monomer A / monomer B described above is also preferred. More preferably, the road bitumen comprises the chemical additive of formula (II) where m = 0, more preferably where m = 0 and n = 0 and the olefinic polymer admixture chosen from terpolymers (b) ethylene / monomer A / monomer B described above. - The coating layer / second composition: According to the invention, the coating layer is obtained by application of a composition comprising: • at least one viscosifying compound chosen from cellulose ethers, and • at least one anti-caking agent on all or part of the surface of the bitumen core. ICG70142 EN text deposit 36 The precursor composition of the coating layer may comprise at least one solvent to facilitate its application. The terms “viscosifier” and “viscosifying compound” are used within the meaning of the invention, in an equivalent manner and independently of one another. By "viscosifier" or "viscosifying compound" is meant a compound which has the property of reducing the fluidity of a liquid or of a composition and therefore of increasing its viscosity. The viscosifier within the meaning of the invention is a material which has a dynamic viscosity greater than or equal to 50 mPa.s' 1 , preferably from 50 mPa.s' 1 to 550 mPa.s' 1 , more preferably from 80 mPa. s ' 1 to 450 mPa.s' 1 , the viscosity being a Brookfield viscosity measured at 65 ° C. The viscosity of a viscosifier according to the invention is measured at 65 ° C. using a Brookfield CAP 2000+ viscometer and at a rotation speed of 750 rpm. The measurement is read after 30 seconds for each temperature. The coating layer is solid at high ambient temperature, in particular at a temperature above 60 ° C. According to one embodiment of the invention, the average thickness of the coating layer is preferably greater than or equal to 20 μm, more preferably from 20 to 200 μm, and even more preferably from 40 to 150 μm, and even more preferably from 50 to 100 μm. The coating layer must be thick enough for it to be continuous. In addition to the cellulose ether compound and the anti-caking agent, the coating layer may optionally comprise one or more compounds chosen from: the other viscosifying compounds, the chemical additives which have been described above, the polymers, the plasticizing agents. , surfactants, ... The coating composition preferably comprises, on the basis of its final composition, from 5 to 40% by weight of plasticizer, in particular from 5 to 25% by weight, with a content by weight of 5 to 20% more preferably . It is possible to use a conventional plasticizer for this in film coating compositions. Among the plasticizing agents, mention may be made of fatty acids, such as, for example, stearic acid, or mixtures of fatty acids, such as the product sold under the brand name Miglyol®. According to a preferred embodiment, the coating layer essentially consists of: • one or more viscosifying compounds chosen from cellulose ethers, and • at least one anti-caking agent. ICG70142 EN text deposit 37 Advantageously, according to this embodiment, the coating layer comprises, or better still consists essentially of: ° one or more cellulose ethers and ° at least 10% of one or more anti-caking agents, the percentages being expressed by mass relative to the total mass of the coating layer. Even more advantageously, according to this embodiment, the coating layer comprises, or better still consists essentially of: ° one or more cellulose ethers and ° at least 20%, more preferably at least 30%, advantageously at least 40% and even more advantageously at least 50% of one or more anti-caking agents, the percentages being expressed by mass relative to the total mass of the coating layer. According to another preferred embodiment, the coating layer essentially consists of: • one or more viscosifying compounds chosen from cellulose ethers, • at least one anti-caking agent, and • at least one plasticizing agent. Advantageously, according to this embodiment, the coating layer comprises, or better still consists essentially of: ° one or more cellulose ethers, ° at least 10% of one or more anti-caking agents, • at least one plasticizing agent, the percentages being expressed by mass relative to the total mass of the coating layer. Even more advantageously, according to this embodiment, the coating layer comprises, or better still consists essentially of: ° one or more cellulose ethers and ° at least 20%, more preferably at least 30%, advantageously at least 40% and even more advantageously at least 50% of one or more anti-caking agents, • at least one plasticizing agent , the percentages being expressed by mass relative to the total mass of the coating layer. Advantageously, the second composition is in the form of a solution or of a dispersion in a solvent. ICG70142 EN text deposit 38 The solvent is advantageously chosen from water and mixtures of water and organic solvents miscible with water such as alcohols, for example ethanol, methanol, glycerol. Preferably, the concentration of material other than the solvent in said solutions and / or dispersions is from 50 g / L to 500 g / L, preferably from 75 g / L to 300 g / L and even more preferably from 100 g / L at 250 g / L. "Cellulose ether Cellulose ether is a cellulose derivative in which some or all of the hydroxyl functions of cellulose have reacted with a chemical reagent to form an ether. Other functionalizations of cellulose are possible in addition to the ether functions. The cellulose ether can be in the form of a salt. Among the cellulose ethers there may be mentioned: methyl cellulose, ethylcellulose, hydroxymethylcellulose hydroxyethylcellulose (HEC), hydroxypropylcellulose (HPC), hydroxyethyl methylcellulose (HEMC), hydroxypropyl methylcellulose (HPMC), hydroxybutyl methylcellulose (HBMC), carboxymethylcellulose (CMC), sodium carboxymethylcellulose (Na-CMC), carboxymethylsulfoethylcellulose, hydroxyethylmethylcarboxymethylcellulose. Advantageously, the cellulose ethers are selected from hydrophilic cellulose ethers. Advantageously, the cellulose ethers are chosen from: hydroxyethyl methylcellulose, hydroxypropyl methylcellulose, hydroxybutyl methylcellulose, even more advantageously hydroxypropyl methylcellulose. »The other viscosifying compounds: Preferably, in addition to the cellulose ethers, the viscosifiers are chosen from: - gelling compounds, preferably of plant or animal origin, such as: gelatin, agar-agar, alginates, starches, modified starches, or gellan gums; polyethylene glycols (PEG) such as PEG having a molecular weight of between 800 g.mol ' 1 and 8000 g.mol' 1 , such as for example a PEG having a molecular weight of 800 g.mol ' 1 (PEG- 800), a PEG having a molecular weight of 1000 g.mol ' 1 (PEG-1000), a PEG having a molecular weight of 1500 g.mol' 1 (PEG-1500), a PEG having a molecular weight of 4000 g .mol ' 1 (PEG-4000) or a PEG having a molecular weight of 6000 g.mol' 1 (PEG-6000); - mixtures of such compounds. Advantageously, in addition to the cellulose ethers, the viscosifiers are chosen from: - gelling compounds, preferably of plant or animal origin, such as: gelatin, agar-agar, alginates, gellan gums; ICG70142 EN text deposit 39 polyethylene glycols (PEG) such as PEG having a molecular weight of between 800 g.mol ' 1 and 8000 g.mol' 1 , such as for example a PEG having a molecular weight of 800 g.mol ' 1 (PEG- 800), a PEG having a molecular weight of 1000 g.mol ' 1 (PEG-1000), a PEG having a molecular weight of 1500 g.mol' 1 (PEG-1500), a PEG having a molecular weight of 4000 g .mol ' 1 (PEG-4000) or a PEG having a molecular weight of 6000 g.mol' 1 (PEG-6000); - mixtures of such compounds. »Anti-caking compounds: The anti-caking compound is of mineral or organic origin. The term “anti-caking agent” or “anti-caking compound” means any compound which limits, reduces, inhibits, delays, the agglomeration and / or the adhesion of the granules to one another during their transport and / or their storage at temperature. ambient and which ensures their fluidity during their handling. More preferably, the anti-caking compound is chosen from: talc; fines, also called fillers, generally of diameter less than 125 μm, such as siliceous fines, with the exception of fine limestones; sand such as Fontainebleau sand; cement ; carbon; wood residues such as lignin, lignosulfonate, powders of coniferous needles, powders of coniferous cones, in particular pine; rice husk ash; glass powder; clays such as kaolin, bentonite, vermiculite; alumina such as alumina hydrates; silica; silica derivatives such as silica fumes, functionalized silica fumes, in particular hydrophobic or hydrophilic silica fumes, fumed silicas, in particular hydrophobic or hydrophilic fumed silicas, silicates, silicon hydroxides and silicon oxides ; plastic powder; lime; hydrated lime; the plaster ; rubber crumb; polymer powder, such as styrene-butadiene copolymers (SB), styrene-butadiene-styrene copolymers (SB S) and mixtures of these materials. Advantageously, the anti-caking agent is chosen from talc; fines generally with a diameter of less than 125 µm with the exception of limestone fines, such as siliceous fines; wood residues such as lignin, lignosulfonate, powders of coniferous needles, powders of coniferous cones, in particular pine; glass powder; sand such as Fontainebleau sand; silica fumes, in particular hydrophobic or hydrophilic silica fumes; and their mixtures. - The granules: Within the meaning of the invention, the term “granules of material usable as road binder or as waterproofing binder” can also be defined as a material usable as road binder or as solid waterproofing binder at room temperature conditioned under a ICG70142 FR text deposit 40 divided form, that is to say in the form of small units called granules or particles, comprising a core based on material usable as road binder or as waterproofing binder and an envelope or shell or coating or coating layer or coating. Preferably, the coating layer covering the granules of material which can be used as a road binder or as a sealing binder according to the invention is continuous. Preferably, the coating layer is applied so that at least 90% of the surface of the core of said granules is covered with the coating layer, preferably at least 95%, more preferably at least 99%. According to one embodiment of the invention, the coating layer covering at least part of the surface of the core of the granules represents from 0.2% to 20% by mass, preferably from 0.5% to 15% by mass , more preferably from 1% to 10% relative to the total mass of the core of the granules. Preferably, the granules of material which can be used as a road binder or as a sealing binder, advantageously of bitumen, according to the invention, can have, within the same population of granules, one or more shapes chosen from a cylindrical, spherical shape. or semi-spherical or ovoid, preferably in a semi-spherical form. The size of the granules is such that the longest average dimension is preferably less than or equal to 50 mm, more preferably from 2 to 30 mm, even more preferably from 3 to 20 mm. The size and shape of the granules can vary depending on the manufacturing process used. For example, the use of a die makes it possible to control the manufacture of granules of a chosen size. A sieving makes it possible to select granules according to their size. Preferably, the granules of material which can be used as a road binder or as a sealing binder, advantageously the bitumen granules, according to the invention have a weight of between 0.1 g and 50 g, preferably between 0.2 g and 10 g, more preferably between 0.2 g and 5 g. Without being linked to theory, the Applicant has unexpectedly discovered that the use of a viscosifying compound of the cellulose ether type and of at least one anti-caking agent according to the invention makes it possible to obtain a coating layer: - which is resistant to climatic conditions and to the conditions of transport and / or extreme storage of solid material usable as road binder or as waterproofing binder, - which breaks easily under a mechanical shearing effect, such as for example under the effect of a mechanical shearing applied in a tank such as a kneader or a drum-kneader during the manufacture of mixes, - which does not require an additional step after its application. More particularly, the coating layer resists the transport and / or storage of the material which can be used as a road binder or as a sealing binder, in particular bitumen, at high ambient temperature, in particular at a temperature above 60 ° C., in " Big ICG70142 EN text deposit 41 Bags "while being brittle under the effect of mechanical shearing. It thus allows the release of the heart during the manufacture of asphalt. According to one embodiment of the invention, the bitumen granules may further comprise one or more other coating layers covering all or part of the coating layer of the solid material usable as road binder or as waterproofing binder, in particular bitumen, according to the invention. - Granules manufacturing process: Another subject of the invention relates to a method for manufacturing granules of solid material which can be used as a road binder or as a sealing binder, in particular bitumen, composed of a core and a coating layer of the core, this method comprising : i) shaping the heart from at least one first composition, ii) coating the heart over all or part of its surface with at least one second composition comprising at least one viscosifying compound chosen from cellulose ethers and at least one anti-caking compound. Step ii) can be carried out by soaking, spraying, co-extrusion, etc. Preferably, step ii) is carried out by a method using a fluidized air bed device. Fa shaping of the core of the granules from a solid material which can be used as a road binder or as a sealing binder, in particular bitumen, can be produced according to any known process, for example according to the manufacturing process described in the document US 3,026,568, WO 2009/153324 or WO 2012/168380. According to a particular embodiment, the shaping of the core of solid material can be carried out by draining, in particular using a drum. Other techniques can be used in the manufacturing process of the core of solid material, in particular molding, pelletizing, extrusion ... The coating of the granules of solid material which can be used as a road binder or as a sealing binder, in particular bitumen, can be done by any known technique, in particular by applying the second material in a fluidized bed process, as described for example in US -5,236,503 or in EP 1 407 814. Preferably, the particles of core of solid material have a longest average dimension ranging from 1 to 30 mm, advantageously from 2 to 20 mm, even more advantageously from 2 to 10 mm. Preferably, during the implementation of the method of the invention, the mass ratio of the coating layer relative to the mass of core, possibly additive, is from 0.05 to 1, advantageously from 0.1 to 0.9, even more advantageously from 0.1 to 0.5. ICG70142 EN text deposit 42 Another object of the invention consists of granules of solid material which can be used as a road binder or as a sealing binder, in particular bitumen, capable of being obtained by implementing the method according to the invention as described below. above. Advantageously, such granules have the properties described above. - Uses of granules: Another object of the invention also relates to the use of the granules according to the invention as a road binder. Fe road binder can be used to manufacture asphalt, in combination with aggregates according to any known process. Preferably, the granules of solid material which can be used as a road binder or as a waterproofing binder, in particular of bitumen, according to the invention, are used for the manufacture of mixes. Bituminous or non-bituminous coated materials are used as materials for the construction and maintenance of pavement bodies and their coating, as well as for the performance of all road works. Mention may be made, for example, of surface coatings, hot mixes, cold mixes, cold cast mixes, severe emulsions, base, bonding, bonding and surface layers, and other combinations of '' a bituminous or non-bituminous binder and road aggregate having particular properties, such as anti-rutting layers, draining asphalt, or asphalts (mixture between a bituminous binder and aggregates of the sand type). Another object of the invention relates to a process for the manufacture of mixes comprising at least one road binder and aggregates, the road binder being chosen from the granules of solid material according to the invention, this process comprising at least the steps of: - heating the aggregates at a temperature ranging from 100 ° C to 180 ° C, preferably from 120 ° C to 160 ° C, - mixing of the aggregates with the road binder in a tank such as a kneader or a kneading drum, - obtaining mixes. Fe process of the invention has the advantage of being able to be implemented without prior step of heating the granules of solid material. The process for manufacturing asphalt mixes according to the invention does not require a step of heating the granules before mixing with the aggregates because, in contact with the hot aggregates, the granules melt. The granules of solid material which can be used as a road binder or as a sealing binder, in particular of bitumen, according to the invention as described above have the advantage of being able to be added directly to the hot aggregates, without having to be melted beforehand. mix with hot aggregates. ICG70142 EN text deposit 43 Preferably, the step of mixing the aggregates and the road binder is carried out with stirring, then the stirring is maintained for at most 5 minutes, preferably at most 2 minutes to allow a homogeneous mixture to be obtained. Fes granules according to the present invention are remarkable in that they allow the transport and / or storage and / or handling of road bitumen at high ambient temperature under extreme conditions, in particular without agglomeration and / or adhesion of the granules of solid material during their transport and / or their storage and / or their handling. Furthermore, the coating layer of the granules breaks under the effect of contact with the hot aggregates and of the shearing and it releases the composition forming the heart. Finally, the presence of the coating layer in the mixture of road binder and aggregates does not degrade the properties of said road bitumen for road application, compared to an uncoated core composition. - Method of transport and / or storage and / or handling of solid material usable as road binder or as coating binder Fes granules obtained by the process of the invention can be transported and / or stored and / or handled in the form of granules of solid material, especially bitumen, solid at room temperature. Fe solid material, including road bitumen, can be transported and / or stored at a high ambient temperature for a period greater than or equal to 2 months, preferably 3 months. Preferably, the high ambient temperature is from 20 ° C to 90 ° C, preferably from 20 ° C to 80 ° C, more preferably from 40 ° C to 80 ° C, even more preferably from 40 ° C to 60 ° C . Fes granules of solid material, especially bitumen, obtained by the process according to the invention have the advantage of retaining their divided form, and therefore of being able to be handled, after storage and / or transport at a high ambient temperature. In particular, they have the capacity to flow under their own weight without leaking, which allows them to be stored in packaging in bags, drums or containers of all shapes and all volumes and then transferred from this packaging to equipment, as site equipment (tank, mixer etc ...). The granules of solid material, in particular of bitumen, are preferably transported and / or stored in bulk in bags of 1 kg to 100 kg or from 500 kg to 1000 kg commonly called in the field of road bitumen "Big Bag". », Said bags preferably being made of hot-melt material. They can also be transported and / or stored in bulk in boxes of 5 kg to 30 kg or in drums of 100 kg to 200 kg. The different embodiments, variants, preferences and advantages described above for each of the objects of the invention apply to all of the objects of the invention and can be taken separately or in combination. ICG70142 FR text deposit 44 Figures: Figure 1: sectional view of the installation with a fluidized air bed Referring to FIG. 1, the installation (10) with a fluidized air bed (12) (also called a granulator) comprises a process chamber (II) with a fluidized air bed (12) in which the cores in one bituminous material (14) are placed and in which an air stream (16) is brought from below to the fluidized bed (12) and through a perforated grid (13) in order to maintain the fluidized bed and in order to dry and / or cool the shells formed around the hearts of bituminous material (14). A precursor composition of the coating layer (18) is then brought to the fluidized bed by means of a spray nozzle (20) opening out from below into the fluidized bed (12). The fluidized bed process chamber (II) (12) also comprises an insert (22) situated above the spray nozzle (20) and in the form of a cylindrical installation part adjustable in height and in diameter and the lower edges (15) of which are adjustably distant from the perforated grid (13) of the bottom of the fluidized bed (12). The filtration chamber (IV) with a fluidized bed (12) comprises several filters (24) making it possible to recycle the fine particles emitted during the implementation of the process. The air flow (16) supplied to the fluidized bed (12) is guided by an incoming air box (I) comprising an incoming air chamber (26). The fluidized air bed granulator (12) thus comprises 4 distinct zones: (I) the inlet air box, (II) the process chamber, (III) the expansion chamber and (IV) the filtration. The area of the fluidized bed formed by the incoming air chamber (26) has an area (28) with a higher flow speed of the air stream (16) applied to the cores of bituminous material (14). The precursor composition of the coating layer (18) is brought into the zone (28) operating at a higher flow rate. The cores of bituminous material (14) coming from the zone (28) with a higher flow speed are brought back to the fluidized bed (12). A part of the bituminous material cores (14) present in the fluidized bed (12) is brought back into the zone (28) at a higher flow speed, so that a circulation of bituminous material cores (14) appears. between the fluidized bed (12) and the area (28). F'invention is illustrated by the following examples given without limitation. Experimental part : In these Examples, the parts and percentages are expressed by weight unless otherwise indicated. ICG70142 EN text deposit 45 Material and method : • Fluidized air bed device: Installation 1: The installation 1 is a fluidized air bed installation used in the process for manufacturing the granules according to the invention. The following examples 1 to 6 were produced in a fluidized air bed granulator sold by the company Glatt under the trade name ProCelF and the cross-section of which is shown in FIG. 1. • Raw materials : The cores of bituminous material used as raw material in the examples below are composed of: Bitumen base (B) - A 50/70 grade bitumen base, noted Bi, having a P25 penetration of 58 1/10 mm and a TBA of 49.6 ° C and commercially available from the TOTAL group under the brand AZALT® Additive: - Al additive of formula (I): sebacic acid - Additive A2 of formula (II): N, N'-ethylenedi (stearamide) sold by the company Croda under the name Crodawax 140 ® Fillers: mineral fillers with a diameter less than or equal to 0.063 mm Preparation of granule cores • Composition: Cl Bitumen base B1 Al 1.5% A2 2.5% Table 1: composition of the bituminous binder constituting the core of the granules The amounts are expressed as a percentage by mass of additive compound relative to the total mass of the composition. ICG70142 EN text deposit 46 • Process: Preparation of the binder base: The bitumen base (Bi) is introduced into a reactor maintained at 160 ° C. with stirring at 300 rpm for two hours. The additives are then introduced into the reactor. Fe content of the reactor is maintained at 160 ° C with stirring at 300 rpm for 1 hour. Preparation of solid binder granules A, General method for the preparation of hearts by binding granules according to the invention The binder composition is heated at 160 ° C for two hours in the oven before being poured into a silicone mold having different spherical holes so as to form the hearts of solid binder. After having observed the solidification of the binder in the mold, the surplus is leveled off with a heated blade with a bunsen burner. After 30 minutes, the solid binder in the form of uncoated granules is removed from the mold and stored in a tray covered with silicone paper. The hearts are then left to cool, binding at room temperature for 10 to 15 minutes. B, General method for the preparation of bitumen cores of the granules according to the invention with an industrial process For the implementation of this method, one can use a device and a method as described in great detail in US Pat. No. 4,279,579. Various models of this device are commercially available from the company Sandvik under the trade name of Rotoform ®. Bitumen granules can also be obtained from the bituminous composition according to the invention poured into the tank of such a device and maintained at a temperature between 130 and 160 ° C. A nozzle or several injection nozzles allow) the transfer of the bitumen composition according to the invention inside the double pastillation drum comprising an external rotary drum, the two drums being equipped with slots, nozzles and orifices allowing the pastillation of bitumen drops through the first fixed drum and orifices having a diameter between 2 and 8 mm from the rotary external drum. The bitumen drops are deposited on the upper face of a horizontal tread, driven by rollers. Bitumen granules were obtained from the bituminous composition C1 poured into the tank of such a device and maintained at a temperature between 130 and 160 ° C. ICG70142 EN text deposit 47 A nozzle or several injection nozzles allows (tent) the transfer of the bituminous composition C1 inside the double pastillation drum comprising an external rotary drum, the two drums being equipped with slots, nozzles and orifices allowing the pastillation of bitumen drops through the first fixed drum and orifices having a diameter between 2 and 8 mm from the external rotary drum. The bitumen drops are deposited on the upper face of a horizontal tread, driven by rollers. Preparation of the coating layer The precursor composition of the coating layer is an aqueous composition comprising: a viscosifying agent: hydropropylmethylcellulose introduced in the form of SEPIFIFM® FP 010 commercially available from the company SEPPIC, and - an anti-caking agent: siliceous fines from FaNoubleau. It is prepared by mixing the components at room temperature in water with the contents of the materials set out in Table 2. Coating of the granules: The bituminous material cores are loaded into the process chamber of the device in FIG. 1, the air flow being in operation. The bituminous material cores are thus fluidized by the air flow injected into the process chamber. Finally, the precursor composition of the coating layer is sprayed into the process chamber through the spray nozzle. Granule load resistance test This test is carried out in order to evaluate the resistance to load of the granules at a temperature of 65 ° C. under a compressive force. Indeed, this test makes it possible to simulate the temperature and compression conditions of the granules one on the other to which they are subjected during transport and / or storage in bulk in bags of 10 to 100 kg or in Big Bags of 500 to 1000 kg or in 200 kg drums and assess their resistance under these conditions. The load resistance test is carried out according to the following protocol: 5 ml of granules are placed in a 20 mF syringe then the piston is placed on the granules as well as a mass of 208 g, representing an applied force as in a Big Bag. Fe everything is placed in the oven at 65 ° C for at least 4 hours. 1. Preparation of bitumen granules with coating layer Experiments 1 to 6 are carried out in the device 10 represented in FIG. 1 The parameters for carrying out the various experiments are given in table 2 below. The spray pressure (in bars) is 1 to 3 bars. ICG70142 EN text deposit 48 Table 2 Examples 1 2 (Q 3 (Q 4 (*) 5 6 Precursor composition of the coating layer % of agentviscosifier - 10 10 10 7.5 10 % anti-caking agent 20 - - - 12.5 10 Conditions for implementing the process Quantity of heartsfluidized(in g) 1050 937 1305 1107 1123 Quantity of precursor composition sprayed (in g) 1003 407 194 224 1060 1000 Fluidization flow (in m 3 / h) 300 300 280 280 250 250 Product temperature (in ° C) 35 35 35 35 17 17 Flow ofspraying (in g / min) 25.1 22.6 10.8 3.3 15.4 14.1 (*) following the agglomeration of the granules during the process, it was interrupted before 5 having sprayed all of the precursor composition. Examples 1 to 4 are counter-examples. Examples 5 and 6 are examples according to the invention. 2. Bitumen granules obtained The granules obtained in Examples 1 to 6 are then evaluated according to several criteria: 1) obtaining bitumen granules comprising a core and a coating layer, 2) the homogeneity of the coating layer formed, 3) deformation of the granules, 4) the presence of agglomerates, and 5) their resistance to high temperature at 65 ° C. ICG70142 EN text deposit 49 The results are shown in Table 3 below. Table 3 Examples 1 2 3 4 5 6 Granule formation Yes no no no Yes Yes Temperature resistanceambient at 65 ° C - - - - ++ +++ +++: the granules retain their original shape and do not adhere to each other. ++: the granules do not adhere to each other but no longer have their rounded shape. +: the granules adhere slightly to each other. : the granules are agglomerated. • Coating layer comprising exclusively an anti-caking agent (example 1) In Example 1, the precursor composition of the coating layer only comprises an anti-caking agent. It can be seen that the bitumen granules obtained according to Example 1 are not stable at high temperature. The mere presence of an anti-caking agent in the precursor composition of the coating layer does not make it possible to obtain bitumen granules which are stable at high temperature. • Coating layer comprising only a viscosifying agent chosen from cellulose ethers (examples 2, 3, 4) In Examples 2, 3 and 4, the precursor composition of the coating layer exclusively comprises a viscosifying agent chosen from cellulose ethers. The cores and the precursor composition of the coating layer sprayed into the process chamber stick to each other without forming granules. These hearts aggregate and make it impossible to form bitumen granules. The mere presence of a viscosifying agent chosen from cellulose ethers in the precursor composition of the coating layer does not make it possible to obtain well individualized bitumen granules. • Coating layer comprising both a viscosifying agent chosen from cellulose ethers and an anti-caking agent (examples 5 and 6) In Examples 5 and 6, the precursor composition of the coating layer comprises both a viscosifying agent chosen from cellulose ethers and an anti-caking agent. ICG70142 FR text deposit 50 The bitumen granules formed in Examples 5 and 6 have good resistance to conditioning at an ambient temperature of 65 ° C. insofar as they hardly adhere to each other. The granules formed in Example 6 are particularly advantageous in that they retain their initial shape. Thus, the handling and transport / storage of said granules formed by the process according to the invention will be easy insofar as the granules and do not agglomerate with each other at high ambient temperature. ICG70142 EN text deposit 51
权利要求:
Claims (15) [1" id="c-fr-0001] 1. Granules of material which can be used as a road binder or as a waterproofing binder comprising a core and a coating layer, in which: the core consists of a first composition comprising at least one material chosen from: a bitumen base, a pitch, a clear binder, and - the coating layer consists of a second composition which comprises: • at least one viscosifying compound chosen from cellulose ethers, and • at least one anti-caking agent. [2" id="c-fr-0002] 2. Granules according to claim 1 in which the cellulose ether is chosen from: methyl cellulose, ethylcellulose, hydroxymethylcellulose, hydroxyethylcellulose (HEC), hydroxypropylcellulose (HPC), hydroxyethyl methylcellulose (HEMC) , hydroxypropyl methylcellulose (HPMC), hydroxybutyl methylcellulose (HBMC), carboxymethylcellulose (CMC), sodium carboxymethylcellulose (Na-CMC), carboxymethylsulfoethylcellulose, hydroxyethylmethylcarboxymethylcellulose. [3" id="c-fr-0003] 3. Granules according to claim 2 in which the cellulose ether is chosen from: hydroxyethyl methylcellulose, hydroxypropyl methylcellulose, hydroxybutyl methylcellulose, even more advantageously hydroxypropyl methylcellulose. [4" id="c-fr-0004] 4. Granules according to any one of the preceding claims, in which the second composition comprises at least 10% of one or more anti-caking agents, the percentages being expressed by mass relative to the total mass of the second composition. [5" id="c-fr-0005] 5. Granules according to any one of the preceding claims in which the anti-caking compound is chosen from: talc; fines generally less than 125 µm in diameter, such as siliceous fines, with the exception of limestone fines; sand such as Fontainebleau sand; cement ; carbon; wood residues such as lignin, lignosulfonate, powders of coniferous needles, powders of coniferous cones, in particular pine; rice husk ash; glass powder; clays such as kaolin, bentonite, vermiculite; alumina such as alumina hydrates; silica; silica derivatives such as silica fumes, functionalized silica fumes, in particular hydrophobic or hydrophilic silica fumes, fumed silicas, in particular hydrophobic or hydrophilic fumed silicas, silicates, silicon hydroxides and silicon oxides ; plastic powder; lime; hydrated lime; the plaster ; blowing snow ICG70142 FR text deposit 52 of rubber; polymer powder, such as styrene-butadiene copolymers (SB), styrene-butadiene-styrene copolymers (SB S) and mixtures of these materials. [6" id="c-fr-0006] 6. Granules according to any one of the preceding claims in which the first composition has a needle penetration measured at 25 ° C according to standard EN 1426 from 5 to 330 1/10 mm, preferably from 10 to 220 1 / 10 mm. [7" id="c-fr-0007] 7. Granules according to any one of the preceding claims, in which the first composition further comprises at least one chemical additive chosen from: an organic compound, a paraffin, a polyphosphoric acid, an adhesion dope and their mixtures. [8" id="c-fr-0008] 8. A method of manufacturing granules of material usable as a road binder or as a sealing binder composed of a core and a coating layer of the core according to any one of the preceding claims, this method comprising: i) the shaping of the heart from a first composition comprising at least one material chosen from: a bitumen base, a pitch, a clear binder, ii) the coating of the heart on all or part of its surface with a second composition comprising at least one viscosifying compound chosen from cellulose ethers and at least one anti-caking agent. [9" id="c-fr-0009] 9. The method of claim 8 wherein the second composition is applied to the heart of the granules in a fluidized air bed device. [10" id="c-fr-0010] 10. Granules of material which can be used as a road binder or as a sealing binder, capable of being obtained by implementing the method according to claim 8 or according to claim 9. [11" id="c-fr-0011] 11. Granules according to any one of claims 1 to 7 and 10 which have a stability in transport and / or storage and / or handling at a temperature up to 100 ° C, advantageously from 20 ° C to 90 ° C, preferably from 20 ° C to 80 ° C, more preferably from 40 ° C to 80 ° C, even more preferably from 40 ° C to 60 ° C, for a period greater than or equal to 2 months, preferably greater or equal to 3 months. [12" id="c-fr-0012] 12. Use of the granules according to any one of claims 1 to 7, 10 and 11 as a road binder. [13" id="c-fr-0013] 13. Use according to claim 12 for the manufacture of mixes. ICG70142 EN text deposit 53 [14" id="c-fr-0014] 14. Process for the manufacture of mixes comprising at least one road binder and aggregates, the road binder being chosen from the granules according to any one of claims 1 to 7, 10 and 11, this process comprising at least the steps of: heating the aggregates at a temperature ranging from 100 ° C. to 180 ° C., preferably 5 120 ° C to 160 ° C, - mixing of the aggregates with the road binder in a tank such as a kneader or a kneading drum, - obtaining mixes. 15. The method of claim 14, which does not include a step of heating the road binder before it is mixed with the aggregates. 16. Method of transport and / or storage and / or handling of material usable as road binder or as waterproofing binder, said material being transported and / or stored [15" id="c-fr-0015] 15 and / or handled in the form of granules according to any one of claims 1 to 7, 10 and 11. 1/1
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同族专利:
公开号 | 公开日 EP3612616A1|2020-02-26| US20200165458A1|2020-05-28| WO2018193210A1|2018-10-25| FR3065464B1|2019-06-28|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US20110233105A1|2008-08-29|2011-09-29|Billian I.P. Limited|Asphalt pellets| US20160222542A1|2013-09-16|2016-08-04|Commissariat A L'energie Atomique Et Aux Energies Alternatives|Substrate with low-permeability coating for the solidification of silicon| WO2016198782A1|2015-06-09|2016-12-15|Total Marketing Services|Bitumen that is solid at ambient temperature| US3026568A|1958-11-14|1962-03-27|Schuller Services Ltd|Method for producing coated bitumen pellets| EP0012192B1|1978-12-08|1983-01-12|Santrade Ltd.|Device for extruding fluid masses from a container| GB8508613D0|1985-04-02|1985-05-09|British Petroleum Co Plc|Chemical process| US5236503A|1991-10-28|1993-08-17|Glatt Air Techniques, Inc.|Fluidized bed with spray nozzle shielding| FR2739863B1|1995-10-16|1997-11-21|Elf Antar France|PROCESS FOR THE PREPARATION OF BITUMEN / POLYMER COMPOSITIONS WITH REINFORCED MULTIGRADE CHARACTER AND APPLICATION OF THE COMPOSITIONS OBTAINED IN THE PRODUCTION OF BITUMEN / POLYMER BINDERS FOR COATINGS| FR2804125B1|2000-01-24|2002-10-25|Total Raffinage Distribution|BITUMINOUS BINDER, COLORED COMPOSITIONS OBTAINED FROM THIS BINDER AND THEIR APPLICATIONS| US6835756B2|2000-10-13|2004-12-28|Bp Exploration Operating Company Ltd.|Fischer-tropsch synthesis process| ES2271313T5|2001-07-27|2011-01-20|Sasol Technology Limited|WAX PRODUCTION PRODUCED BY FISCHER-TROPSCH SYNTHESIS.| EP1407814B1|2002-09-28|2014-05-07|Glatt Ingenieurtechnik GmbH|Process and apparatus with a fluidised bed apparatus for producing granules| EP1473327A1|2003-05-01|2004-11-03|KRATON Polymers Research B.V.|A colorable composition| EP1783174B1|2005-11-04|2012-03-07|Latexfalt B.V.|Binder composition comprising a low viscosity naphthenic oil for coloured hot-mix asphalt applications| WO2007058994A2|2005-11-14|2007-05-24|Kraton Polymers Research B.V.|Process for preparing a bituminous binder composition| JP5325207B2|2007-05-01|2013-10-23|クレイトン・ポリマーズ・ユー・エス・エル・エル・シー|Bitumen binder composition and method for preparing the same| FR2932487B1|2008-06-12|2010-08-27|Total France|CLEAR SYNTHETIC BINDER EMULSION.| US20110115116A1|2008-06-20|2011-05-19|De Amorim Novais Da Costa Nobrega Joao Miguel|Method for preparing coated binder units| FR2938547B1|2008-11-14|2012-11-16|Total Raffinage Marketing|CLEAR SYNTHETIC BINDER| FR2948677B1|2009-07-29|2011-09-16|Total Raffinage Marketing|PROCESS FOR THE PREPARATION OF BITUMEN / POLYMERIC COMPOSITIONS RETICULATED WITHOUT RETICULATING AGENT| CN103597035B|2011-06-07|2016-03-16|国际壳牌研究有限公司|Prepare the method for coating and bonding agent unit| FR3024456B1|2014-08-01|2016-08-19|Total Marketing Services|BITUMEN GRANULES|US10907353B2|2017-12-15|2021-02-02|Owens Coming Intellectual Capital, LLC|Polymer modified asphalt roofing material| CA3122562A1|2018-12-10|2020-06-18|Owens Corning Intellectual Capital, Llc|Roofing shingle composition| US20220017749A1|2018-12-10|2022-01-20|Total Marketing Services|Bituminous composition solid at ambient temperature| WO2020120314A1|2018-12-10|2020-06-18|Total Marketing Services|Bituminous composition solid at ambient temperature| CN110193893B|2019-06-28|2020-06-23|四川大学|Preparation method of polymer-based spherical powder|
法律状态:
2018-03-22| PLFP| Fee payment|Year of fee payment: 2 | 2018-10-26| PLSC| Search report ready|Effective date: 20181026 | 2020-03-19| PLFP| Fee payment|Year of fee payment: 4 | 2021-04-23| PLFP| Fee payment|Year of fee payment: 5 |
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申请号 | 申请日 | 专利标题 FR1753473|2017-04-21| FR1753473A|FR3065464B1|2017-04-21|2017-04-21|SOLID BITUMEN AT AMBIENT TEMPERATURE|FR1753473A| FR3065464B1|2017-04-21|2017-04-21|SOLID BITUMEN AT AMBIENT TEMPERATURE| PCT/FR2018/050973| WO2018193210A1|2017-04-21|2018-04-18|Bitumen solid at ambient temperature| EP18722687.3A| EP3612616A1|2017-04-21|2018-04-18|Bitumen solid at ambient temperature| US16/606,943| US20200165458A1|2017-04-21|2018-04-18|Bitumen solid at ambient temperature| 相关专利
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