• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention relates to the use of graphene materials of high aspect ratio and low thickness for the improvement of impact resistance, elongation or fluidity index of thermoplastic materials, mixtures of thermoplastic materials or thermoplastic materials reinforced with other types of loads or fibers. A high ratio and aspect results in an improvement in the polymeric material graphene interface and greater matrix-reinforcement interaction due to the greater contact surface and allowing the polymer chains to exhibit high freedom of movement resulting in improved resistance to impact, elongation or flow rate and in many cases an improvement of 2 or 3 of the aforementioned characteristics. (Machine-translation by Google Translate, not legally binding)
    公开号:ES2725319A1
    申请号:ES201830285
    申请日:2018-03-23
    公开日:2019-09-23
    发明作者:Cordon Julio Gomez；Martinez Javier Perez；Jimenez Luis Otano
    申请人:Avanzare Innovacion Tecnologica S L；
    IPC主号:
    专利说明:

    [0001]
    [0002] USE OF GRAPHENIC MATERIALS OF ELEVATED ASPECT RELATIONSHIP AS ADDITIVES OF THERMOPLASTIC MATERIALS.
    [0003]
    [0004] SECTOR OF THE TECHNIQUE
    [0005]
    [0006] The present invention relates to the use of graphene materials as additives in thermoplastic matrices and which allow to increase at least one of the following characteristics, elongation, flow rate or impact resistance.
    [0007]
    [0008] BACKGROUND OF THE INVENTION
    [0009]
    [0010] Graphene materials are a family of sheet materials, or two-dimensional, of low thickness, between 1 and 10 layers, as described in the editorial article of Professor Bianco (CARBON 65, 2013, 1-6). Six working principles are established and it provides the necessary nomenclature to correctly and systematically define the different graphene materials:
    [0011]
    [0012] - Graphene sheet or monolayer graphene sheet (monolayer): Sheet of a thick atom, hexagonal arrangement where the carbon atoms that compose it show sp2 type bonds.
    [0013] - Graphene microllamine: adapts to the previous definition, and its use is recommended for cases where the lateral size is between 100 nm and 100 pm.
    [0014] - Bilayer / 3-layer graphene: two-dimensional materials composed of 2 or 3 layers.
    [0015] - Multilayer graphene (multilayer): material composed of between 2 and approximately 10 layers of graphene.
    [0016] - Graphene of few layers (fewlayers): material composed of between 2 and 5 layers of graphene.
    [0017] - Graphite nanoparticles or nanolamines: materials with graffiti arrangement that have a dimension smaller than 100 nm (can be the thickness or lateral size).
    [0018] - Exfoliated graphite: Material obtained by a partial exfoliation of graphite or graphite intercalation materials (thermal, mechanical or chemical), with a 3D structure (thickness greater than 10 layers).
    [0019] - Graphene oxide (GO): chemically modified graphene by massive oxidation of the plane; being a single layer material with a high oxygen content. The C / O atomic ratio can be close to 2 (or up to 3).
    [0020] - Multilayer graphene oxide: this name is proposed in the materials in which there is a reaglomeration of the sheets or a complete exfoliation; considering a maximum of 10 sheets.
    [0021] - Graphite oxide: material in which the sheets have been modified and functionalized, increasing the space between them. This material can be partially delaminated to obtain graphene oxide of few layers or fully exfoliated until it reaches graphene oxide. Graphene and graphite oxides are characterized by presenting a diffraction peak of X-ray diffraction different from the rest, (001) compared to (002) of the reduced or pristine ones.
    [0022] - Reduced graphene oxide (rGO): it is the material obtained after applying reduction processes (they can be thermal, chemical, photochemical treatments, by microwaves or microorganisms.
    [0023] - Functionalized graphene materials. For this type of decorations or functionalizations it is proposed to include the type of molecule that functionalizes it. For example: reduced graphene oxide microllamine functionalized with aminopropylsilane.
    [0024]
    [0025] Thus, for example, a reduced graphene oxide with an average number of layers of 7 will be called multilayer reduced graphene oxide and if the average number of layers is between 2 and 5 it will be called a few layers of reduced graphene oxide.
    [0026]
    [0027] Graphene materials have a very high aspect ratio, because their thickness is very low, being between 0.35 nm for a graphene monolayer or a reduced graphene oxide monolayer, to a maximum thickness of 10 nm that could present a multilayer of graphene oxide. The lateral size is usually small, for example for materials produced by exfoliation in liquid medium, such as those developed by Professor Coleman (Nature Materials 2014, 13, 624-630); to very high as for example the graphene material AVA18 in "Application of graphene-based flexible antennas in consumer electronic devices" Materials Today, 2018, doi.org/10.1016/j.mattod.2018.01.007. The aspect ratio is calculated by dividing the average lateral size by the average thickness.
    [0028]
    [0029] As mentioned, there are other related materials of greater thickness such as graphite oxide, which has more than 10 layers, or so-called graphene or graphite nanolamines, which have an average thickness greater than 3.5 nm and So more than 10 layers.
    [0030] In 2014 another publication "Classification Framework for Graphene-Based Materials" appeared. Angew Chem. Int. Ed. 2014, 53, 7714-7718, in which a model is proposed for classification according to three characteristics of the material: Number of layers, Average lateral size, Atomic ratio C / O.
    [0031]
    [0032] The lateral size is the size in the graphene plane. A larger lateral size will produce a better interaction with the matrix. The size measurement, lateral of the graphene material, can be carried out by various techniques, both in powder and in a processed sample, for example in solution. However, this sample processing can alter it avoiding a correct characterization of it. For these reasons the use of laser diffraction of solid samples is a tool for their characterization. Percentiles are used in this type of measure, the D50 percentile being the most common, which refers to the value of the particle size for which 50% of the distribution is of a smaller size.
    [0033]
    [0034] Most studies have shown that adding rigid fillers, such as inorganic filler fillers, results in the decrease of certain mechanical and rheological properties of polymers when they are compared to pure polymer. The properties that usually decrease are usually the flow rate, elongation and impact. This is due to the fact that the loads that, being rigid, give rise to restrictions in the rearrangement of the polymer chains of the matrix and transfer this stiffness to the polymer, resulting in a decrease in elongation and impact resistance, increasing also the viscosity in the molten state, whereby the flow rate decreases.
    [0035]
    [0036] The impact toughness of plastics can be improved by adding impact modifiers. And to improve the flow rate and elongation, plasticizers are used.
    [0037]
    [0038] Plasticizing materials are used to improve elongation, the vast majority of them organic compounds; Handbook of Plasticizers (Third Edition), George Wypych, ISBN: 978-1 895198-97-3; or of natural origin European Polymer Journal 2011, 47, 254-263. Graphene materials, such as graphene oxide or functionalized materials have lubricating characteristics as described for example in CN105112124 or in Tribol Lett 2014, 56, 133 142.
    [0039]
    [0040] Impact modifiers are usually elastic materials that can absorb loads efficiently, usually because they have a long and flexible chain in their structure. In Plastics, Additives and Compounding 2004, 6, 46-49 and in Greco R. (1998) "Impact modifiers: (1) mechanisms and applications in thermoplastics". Pritchard G. (eds) Plastics Additives. Polymer Science and Technology Series, vol 1. 978-94-010-6477-4, are described alternatives for a large number of thermoplastics and the mechanisms associated with the improvement of impact resistance. Examples of formulations of thermoplastic materials with impact modifiers are polymer blends, usually a rigid thermoplastic and an elastomer, with PP-EPDM or HIPS being one of the formulations most used by the industry, which are polystyrene modified with elastomeric materials . Also, mixtures with other polyolefins are used to improve impact resistance. Examples of this type of modification have been described in the literature for decades (Morphological study on the effect of elastomeric impact modifiers in polypropylene systems. Polymer 1979, 20, 37-43, or in CN106832583)
    [0041]
    [0042] Examples of the use of nanomaterials in improving impact both in mixtures and in thermoplastics have also been described. In US6060549A, the use of exfoliated clays for the improvement of mechanical properties including impact resistance is described. Journal of Applied Polymer Science, 2004, 92, 2714-2723 describes the improvement of impact resistance using n-CaCO3 in both PVC and PVC-chlorinated polyethylene.
    [0043]
    [0044] Other fillers, such as nano-clays and silicates of various morphologies are known and used in a wide range of polymers for the improvement of mechanical properties. In Polymer, 2004, 45,2321-2331, it is described for PA6, significant increases in the module using montmorillonite and modifications thereof, although there is a decrease in elongation and impact resistance when increasing the load percentage, which it is attributed to a poor charge-matrix interaction, the dispersion of the particles and the stiffness of the particle; effect that is observed in both micro and nanocomposites. It is necessary to emphasize that the chemistry of the polymer-charge interface is key to obtaining a composite with good mechanical properties.
    [0045]
    [0046] Different graphene or related materials have been used to improve mechanical properties, however, the incorporation of these materials causes a decrease in elongation, for example in POLYM. COMPOS., 2016, 37, 1572-1576; It is described how elongation is lost when incorporating graphene derived materials in a PVC matrix, Polymer 20111, 52, 4001-4010 describes the null effect for very low loads and a drastic decrease when increasing its concentration for composites of PP and in Vacuum 2016, 130, 63-71 a decrease in the flow rate is described in the case of LDPE; in Macromolecular Research 2014, 22, 983-989 when the matrix is polyimide International and in the Journal of Composite Materials 2016, 6, 172-182 polyvinyl alcohol-gelatin. In AIP Conference Proceedings 1914, 150001 (2017); doi: 10.1063 / 1.5016778, is described as the incorporation Some types of graphene materials produce a sharp decrease in both impact resistance and elongation at break.
    [0047]
    [0048] In these materials, the aspect ratio is low and the compatibility and interaction with the matrix very limited, which does not allow for a good dispersion, which results in agglomerates and the loss of properties such as elongation at break, impact resistance and also result in an increase in viscosity and therefore a reduction in the flow rate.
    [0049]
    [0050] OBJECT OF THE INVENTION
    [0051]
    [0052] The object of the present invention is to improve the impact resistance, elongation or fluidity index of thermoplastic materials, mixtures of thermoplastic materials or thermoplastic materials reinforced with other types of fillers or fibers.
    [0053]
    [0054] The invention is based on the use of graphene materials of high aspect ratio as a load of thermoplastic materials so as to at least increase one of the three characteristics: impact resistance, elongation or flow rate
    [0055]
    [0056] The preparation of the composites is based on technologies currently described in the state of the art such as melt mixing, reactive extrusion, in-situ polymerization or solution blending.
    [0057]
    [0058] DESCRIPTION
    [0059]
    [0060] The most common thermoplastic materials are polyolefins such as polyethylene, polypropylene or polybutylene; polyamides, polystyrenes, polylactic acid, thermoplastic polyurethane, polyvinylchloride, polyethylene polyethylene phthalate, polymethyl methacrylate, PTFE, polyoxymethylene, other polyacetals, polycarbonate, polyimides, polyamide imide, polyetherimide, polyether polyether, sulfide Polyacrylonitrile, Vinylidene Polychloride. Also common are the use of mixtures thereof, such as the use of PP-EPDM or the reinforcement thereof by starting fibers such as for example polyamide 6 reinforced with glass fiber or polypropylene with carbon fiber or by fillers such as for example polypropylene with talc or calcium carbonate or polyamides with nano-clays or carbon nanotubes. The use of reinforced mixtures is also very common, such as talc reinforced PP-EPDM
    [0061]
    [0062] In certain industrial applications thermoplastic materials, their mixtures, or reinforced thermoplastics, need an improvement of some characteristics such as elongation at break, to avoid breakage due to stretching or an improvement in impact resistance. For its processability it is necessary to improve the flow rate.
    [0063]
    [0064] Graphene materials are a family of products ranging from pristine graphene to graphene oxide or to functionalized materials thereof.
    [0065]
    [0066] It is essential to take into account the polarity of the polymer and the characteristics of the graphene material we are using.
    [0067]
    [0068] Taking into account the lack of polarity of the carbonaceous graphene skeleton, one option is to work with graphene oxide and its derivatives such as reduced graphene oxide, so that the oxygen positions of the structure provide the material with a certain polarity and, therefore, they improve the compatibility with the matrix. Normally the functional groups are of the type C-OH, COOH, C = O or epoxide.
    [0069]
    [0070] Also the graphene materials produced by liquid phase exfoliation by means of mechanochemical processes or electrochemical exfoliation and these functionalized materials, can be used for the improvement of elongation, impact or improvement of the flow rate in thermoplastic materials. The functional groups are thiols, carboxylic, phosphonic, di or tetrasulfides; amines; chlorosilanes; alkoxysilanes phosphonates, glycols, ammonium, diamines, triamines, tetramanines, sulfosuccinates, aromatic groups, pyridinics, phthalates or sulfates.
    [0071] On the other hand, the improvement of compatibility can be done by introducing functional groups. This functionalization can be covalent and non-covalent depending on the type of link used, and can improve both dispersion and compatibility, achieving a better interface; and therefore, better properties like those described here.
    [0072]
    [0073] The aspect ratio of graphene materials is key, and as discussed will depend on both thickness and lateral size. A high aspect ratio will improve the interaction of the graphene material matrix as there is a greater contact surface.
    [0074]
    [0075] The graphene materials as mentioned are those that have a number of average layers between 1 and 10, these materials are those that have been observed the greatest increase in the mechanical and rheological properties described here. Here it should be noted that these graphene materials have the highest aspect ratio, due to their low thickness. However, for certain materials with higher thicknesses such as those with 1 to 20 sheets of medium thickness, an improvement of these properties has been observed, although not as high as for materials of thickness between 1 and 10 layers of graphene Finally, for thicker materials such as 1 to 30, it observes some improvement in the properties, but the range of the percentages to which they are obtained are much more restricted.
    [0076]
    [0077] The graphene materials of the present invention have an aspect ratio of up to 900,000 and the smallest is that of a material produced by exfoliation in liquid medium that is 100. Its high aspect ratio and low thickness does not hinder the freedom of movement of The polymer chains, which can also have a lubricating effect, which makes it possible to increase some properties such as the flow rate, elongation or impact resistance. Materials with a very high aspect ratio, above 600,000 are very difficult to disperse and process and the necessary load on polymeric materials is low or very low, always less than 2.5%, and in most polymers thermoplastics, less than 0.5%. Graphene materials with an aspect ratio between 300,000 and 900,000 usually have a very low number of layers, between one and three and a very large lateral size, greater than 100 mm. Materials with a lower aspect ratio such as less than 300,000 are easier to work with and disperse graphene materials in the matrix such as that of Example 2 that has a ratio of 70,000, allows to obtain the desired properties at higher load percentages, and it allows to obtain the expected results and the increase of the elongation, the index of fluidity or of the resistance to the impact. Very low aspect ratio materials usually have a very high number of particles, which results in an increase in viscosity and the consequent decrease in the flow rate. Therefore, it is advisable to increase the aspect ratio to 200 and even above 300, a balance between dispersibility-rheology and properties is usually reached.
    [0078]
    [0079] The lateral size of the graphene material used to improve the described characteristics is in the range of 0.05 microns and 300 microns, when the aspect ratios are higher, the optimal lateral size is between 0.1 and 200 microns and in the case of materials derived from graphene oxide, reduced graphene oxide or materials produced by liquid phase exfoliation, the range is restricted to between 0.25 and 150 microns.
    [0080] The graphene materials that can be used for the improvement of elongation, impact resistance or the improvement of the flow rate are graphene oxide, few layers of graphene oxide, multilayer graphene oxide, graphite oxide, reduced graphene oxide, few layers of graphene oxide, reduced, multilayer reduced graphene oxide, reduced graphite oxide, functionalized graphene oxide, few layers of functionalized graphene oxide, functionalized multilayer graphene oxide, functionalized graphite oxide, functionalized reduced graphene oxide, few layers of functionalized graphene oxide, reduced functionalized, oxide of functionalized multilayer reduced graphene, functionalized reduced graphite oxide, or combinations thereof.
    [0081]
    [0082] The concentration of graphene materials as additives of thermoplastic materials for the improvement of these properties can be between 0.001% and 20% by weight. Depending on the type of thermoplastic matrix, surface chemistry from functionalization or oxidation or reduction processes and the aspect ratio, improvements in impact resistance, flow rate or elongation at lower percentages are obtained; Thus, for example, when the lateral size measured by laser diffraction D50 is above 8 microns from 5%, an increase in melt viscosity and loss of elongation at break and impact resistance is observed. that the best properties are obtained at concentrations between 0.001% and 5%. For materials that have a very high aspect ratio and lateral size D50 greater than 15 microns, and because the interaction with the matrix is very high, it is not necessary that the concentration of the graphene material be so high, so that the improvement of the properties usually observed between 0.001% and 2.5% of concentration in weight, in some cases, in which the ratio and aspect is high, and also the lateral size, it is necessary to work at lower percentages, lower than 0.5%, as can be seen in example 3. As already mentioned, the increase from a percentage of concentration, leads to a decrease in elongation, flow rate or impact resistance, therefore concentrations of high graphene material are not recommended or useful.
    [0083]
    [0084] The preparation of the polymer matrix composite using graphene material can be carried out using techniques described in the state of the art such as by in-situ polymerization, solution mixing, melt mixing or reactive extrusion.
    [0085]
    [0086] The polymerization in situ consists of the mixture of the filler, in this case the graphene material, with the pure monomer, a solution of the latter, or in one of the components. Subsequently, a suitable initiator is added and polymerization begins when heat, a catalyst or radiation is applied. The solution mixture consists of the mixture of the charge by agitation or mechanical shearing in the polymer or prepolymer, previously dissolved. The graphene material can be easily dispersed in a suitable solvent and mixed with the polymer dispersion. This graphene-polymer suspension can be precipitated using a non-solvent for the polymer or by evaporation. The mixture in the molten state consists of the mechanical mixture of the polymer in the molten state and the graphene material in the dry powder state or dispersed in a liquid, such as a plasticizer, water or a solvent, applying high shear conditions.
    [0087] EXAMPLES
    [0088]
    [0089] The processes of melt mixing have been carried out in a twin-screw extruder, operating in a counter-rotating direction. The profile of temperatures, characteristics of the spindles, speed of rotation of the spindles and of the feeders, will depend on the polymer used and also on the grapheic material.
    [0090]
    [0091] Continuous threads are obtained from the extrusion that are cooled and cut to obtain the pellet. The pellet obtained is conditioned if necessary, and prepared from the specimens necessary for each test. According to the tests to be carried out on each specimen, a type of specimen is necessary, with dimensions determined by the standard. These specimens are prepared by pressure injection in closed mold.
    [0092]
    [0093] In the case of the measurement of the fluidity index, an extrusion plastometer is used applying the ASTM D 1238-04 standard.
    [0094] The trials of these examples have been developed in the Graphene Flagship Core 1 European Union H2020 Project under grant agreement No. 696656
    [0095] EXAMPLE 1
    [0096]
    [0097] The graphene material consists of a reduced graphene oxide of few layers (average thickness less than 2 nm) and having a lateral size of 43 microns D50. It is surface functionalized with aminosilane groups. The graphene material is melt mixed with Polyamide 6 Ultramid B3K.
    [0098]
    [0099] Dispersions are prepared at various loading percentages and it is characterized:
    [0100]
    [0101]
    [0102]
    [0103] 0 32 17 6
    [0104] 0.05 55 22 14
    [0105] 0.15 51 21 11
    [0106] 0.25 51 18 9
    [0107] 0.50 55 15 8
    [0108] 0.75 58 14 6
    [0109] 1.50 47 4 4
    [0110]
    [0111] EXAMPLE 2
    [0112]
    [0113] The graphene material consists of a reduced graphene oxide of few layers (average thickness between 1 and 2 nm) and having a lateral size of 71 microns D50. The graphene material is melt mixed with Moplen HP500N Polypropylene.
    [0114] Dispersions are prepared at various loading percentages and it is characterized:
    [0115]
    [0116]
    [0117]
    [0118]
    [0119]
    [0120]
    [0121]
    [0122]
    [0123]
    [0124]
    [0125]
    [0126] EXAMPLE 3
    [0127]
    [0128] The graphene material consists of a reduced graphene oxide of few layers (average thickness between 1 and 2 nm) and having a lateral size of 40 microns D50. The graphene material is melt mixed with Moplen EP540P Polypropylene.
    [0129]
    [0130] Dispersions are prepared at various loading percentages and it is characterized:
    [0131]
    [0132]
    [0133]
    [0134]
    [0135] 0.05% 18 496 37
    [0136] 0.10% 19 383 36
    [0137] 0.15% 18 271 34
    [0138]
    [0139] 0.20% 17 23
    [0140] 0.25% 17 176 20
    [0141] 0.30% 14 121 19
    [0142]
    [0143]
    [0144]
    [0145] EXAMPLE 4
    [0146]
    [0147] The graphene material consists of a graphene oxide of few layers (average thickness of 2 nm) and having a lateral size of 41 microns D50. The graphene material is melt mixed with Polyamide 6 Ultramid B3K.
    [0148]
    [0149] Dispersions are prepared at various loading percentages and it is characterized:
    [0150]
    [0151]
    [0152]
    [0153]
    [0154]
    [0155]
    [0156]
    [0157]
    [0158] EXAMPLE 5
    [0159]
    [0160] The graphene material consists of an AVAPLAT7 pristine multilayer graphene (average thickness of 3 nm) and has a lateral size of 7 microns D50. The graphene material is melt mixed with Polyamide 6 Ultramid B3K.
    [0161]
    [0162] Dispersions are prepared at various loading percentages and it is characterized:
    [0163]
    [0164]
    [0165]
    [0166]
    [0167]
    [0168]
    [0169]
    [0170]
    [0171]
    [0172]
    [0173]
    [0174]
    [0175]
    [0176]
    [0177] EXAMPLE 6
    [0178]
    [0179] The graphene material consists of a reduced graphene oxide of few layers (average thickness of 2 nm) and having a lateral size of 21 microns D50. The graphene material is melt mixed with PLA 2003D.
    [0180]
    [0181] Dispersions are prepared at various loading percentages and it is characterized:
    [0182]
    [0183]
    [0184]
    [0185]
    [0186] 0.025 52 8 0.8
    [0187] 0.05 59 7 0.9
    [0188]
    [0189] 0.25 36 6 0.3
    [0190]
    [0191] EXAMPLE 7
    [0192]
    [0193] The graphene material consists of a reduced graphene oxide of few layers (average thickness of 2 nm) and having a lateral size of 21 microns D50. The graphene material is mixed in solution with TPU Elastolan 688AN
    [0194]
    [0195] The TPU is dissolved in DMF and the necessary amount of the reduced graphene oxide is dispersed, ultrasonic and mechanically stirred and the dispersion is precipitated with methanol and dried for 12 hours in an oven at 80 ° C. The residue is processed by melt mixing by extrusion.
    [0196] Dispersions are prepared at various loading percentages and it is characterized:
    [0197]
    [0198]
    [0199]
    [0200]
    [0201]
    [0202]
    [0203]
    [0204]
    [0205]
    1 16 395
    权利要求:
    Claims (1)
    [0001]
    1 The use of graphene materials of high aspect ratio, as additives of thermoplastic materials and which is characterized in that it comprises at least one of the following characteristics:
    a) Improved impact resistance
    b) Elongation improvement
    c) Improvement of the flow rate
    Graphene materials have an aspect ratio between 100 and 900,000 and more preferably between 200 and 600,000 and even more preferably between 300 and 300,000. Graphene materials have an average number of layers between 1 and 30, more preferably between 1 and 20 and even more preferably between 1 and 10.
    2 The use of graphene materials of high aspect ratio, as additives of thermoplastic materials according to claim 1 and characterized in that it comprises the improvement of impact resistance.
    Graphene materials have an aspect ratio between 100 and 900,000 and more preferably between 200 and 600,000 and even more preferably between 300 and 300,000. Graphene materials have an average number of layers between 1 and 30, more preferably between 1 and 20 and even more preferably between 1 and 10.
    The use of graphene materials of high aspect ratio, as additives of thermoplastic materials according to claim 1 and characterized in that it comprises the improvement of elongation
    Graphene materials have an aspect ratio between 100 and 900,000 and more preferably between 200 and 600,000 and even more preferably between 300 and 300,000. Graphene materials have an average number of layers between 1 and 30, more preferably between 1 and 20 and even more preferably between 1 and 10.
    4 The use of graphene materials of high aspect ratio, as additives of thermoplastic materials according to claim 1 and characterized in that it comprises the improvement of the flow rate.
    Graphene materials have an aspect ratio between 100 and 900,000 and more preferably between 200 and 600,000 and even more preferably between 300 and 300,000.
    Graphene materials have an average number of layers between 1 and 30, more preferably between 1 and 20 and even more preferably between 1 and 10.
    The use of graphene materials of high aspect ratio as additives of thermoplastic materials according to claims 1 to 4, wherein the lateral size of the graphene material is in the range of 0.05 microns and 300 microns and more preferably between 0.1 and 200 microns and even more preferably between 0.25 and 150 microns.
    The use of high aspect ratio graphene materials as additives of thermoplastic materials according to claims 1 to 5, wherein the graphene materials are graphene oxide, few layers of graphene oxide, multilayer graphene oxide, graphite oxide, reduced graphene oxide, few layers of graphene oxide, reduced, multilayer reduced graphene oxide, reduced graphite oxide, functionalized graphene oxide, few layers of functionalized graphene oxide, functionalized multilayer graphene oxide, functionalized graphite oxide, oxide of functionalized reduced graphene, few layers of functionalized graphene oxide, reduced functionalized, functionalized multilayer reduced graphene oxide, functionalized reduced graphite oxide, or combinations thereof.
    The use of graphene materials of high aspect ratio as additives of thermoplastic materials according to claims 1 to 6, wherein the graphene materials are pristine or almost-pristine graphene, few layers of pristine or almost-pristine graphene, pristine graphene or multilayer casipristino, produced by liquid phase exfoliation by means of mechanochemical processes or electrochemical exfoliation, being able to be pristine or functionalized.
    The use of graphene materials of high aspect ratio as additives of thermoplastic materials according to claims 1 to 7. In which the functionalization is based on the functional groups are C-OH, epoxide, C = O, thiols, carboxylic, phosphonic , di or tetrasulfides; amines; chlorosilanes; alkoxysilanes phosphonates, glycols, ammonium, diamines, triamines, tetramanines, sulfosuccinates, fluorocarbons, aromatic groups, pyridinics, phthalates or sulfates.
    The use of graphene materials of high aspect ratio as additives of thermoplastic materials according to claims 1 to 8, wherein the concentration of the graphene material is in the range of 0.0001% and 20% by weight and more preferably between 0.001% and 5% by weight and even more preferably between 0.005% and 2.5% by weight.
    The use of graphene materials of high aspect ratio as additives of thermoplastic materials according to claims 1 to 9, wherein the thermoplastic materials they are polyolefins such as polyethylene, polypropylene or polybutylene; polyamides, polystyrenes, polylactic acid, thermoplastic polyurethane, polyvinylchloride, polyester polyethylene phthalate, polymethyl methacrylate, PTFE, polyoxymethylene, other polyacetals, polycarbonate, polyimides, polyamide imide, polyetherimide, polyacrylene ethane, polyurethane ether Polyacrylonitrile, Vinylidene Polychloride, or mixtures thereof or their composites using fillers or fibers and more preferably are polyolefins such as polyethylene, polypropylene or polybutylene; polyamides, polystyrenes or their mixtures or their composites using fillers or fibers.
    11 The preparation of a polymer matrix composite material, using high aspect ratio graphene material according to claims 1 to 10, can be performed using techniques described in the state of the art such as by in-situ polymerization, melt mixing, reactive extrusion or mixing in solution
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    同族专利:
    公开号 | 公开日
    WO2019180292A1|2019-09-26|
    EP3770207A4|2021-12-29|
    ES2725319B2|2020-02-06|
    EP3770207A1|2021-01-27|
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    CN106832583B|2016-01-31|2020-04-24|浙江大学|Impact-resistant polypropylene with high ethylene content and good fluidity and preparation method thereof|CN111187506B|2020-01-15|2021-12-28|青岛科技大学|Method for preparing composite material from graphene nano paste|
    CN111423704B|2020-04-08|2022-02-15|江西师范大学|Polylactic acid stereo complex and preparation method thereof|
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    EP19771072.6A| EP3770207A4|2018-03-23|2019-03-19|Use of high-aspect-ratio graphene materials as additives for thermoplastic materials|
    PCT/ES2019/070182| WO2019180292A1|2018-03-23|2019-03-19|Use of high-aspect-ratio graphene materials as additives for thermoplastic materials|
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