专利摘要:

公开号:ES2772757T9
申请号:ES17176407T
申请日:2015-01-05
公开日:2020-11-24
发明作者:Hans Willi Mainz
申请人:SIG Technology AG;
IPC主号:
专利说明:

[0001] Packaging material, a composite packaging produced from it and a container for the accommodation of packaging material
[0002] The invention relates to a packaging material, in particular packaging wrap, cut-out or a web product rolled into a roll for the manufacture of a packaging, in particular aseptic, consisting essentially of a composite material with at least one layer of cellulose / cardboard, the at least one cellulose / cardboard layer presenting a first sub-zone and at least one second sub-zone, and the at least second sub-zone presenting, in comparison with the first sub-zone, a load of at most half the number-forming units. colonies per gram of cellulose / cardboard of microorganisms or spores, as well as a composite packaging produced from it.
[0003] When, from now on, we speak of "open cutting edges", then this is understood to mean not only the cutting edges that delimit a cut-out or a packaging shell formed from it, but all the "open cellulose areas ", That is, accessible to the surrounding atmosphere, so that in particular cutting edges are also expressed inside perforations such as can be found in beverage containers in the area of fillers to be applied or other auxiliary elements opening.
[0004] The manufacture of composite cardboard / plastic packages takes place either as a so-called "flexible tube forming process" from the roll or from individual scraps of laminated paper / plastic material. In this case, individual cuts are first obtained from a roll of composite material and these are then provided with a watertight longitudinal seam, which is generally produced by folding and sealing the composite material and, if necessary, by gluing. additional top with sealing tape.
[0005] A method is described for the treatment of open cut edges of a packaging wrap, a blank or a web product rolled into a roll of a packaging material, in particular cardboard / plastic composite material, through the placement or introduction of a treatment agent having a sterilizing agent on or within the outer zone of the cutting edges.
[0006] Further processing of packaging casings produced in this way, i.e. closing on one side on the upper or lower side of the subsequent packaging, sterilization, filling and resealing takes place in most cases directly at the filling machine.
[0007] In this case, the shaping of the glass, cleaning and optionally disinfection then take place before the filling material is introduced and the composite packaging is closed and it is finally shaped. Disinfection and filling take place in the case of manufacturing a so-called aseptic composite packaging in the aseptic zone of a filling machine. The shaping of the glass takes place before disinfection or sterilization, the shaping of the glass can also take place outside the aseptic zone. Procedures of this type are described, inter alia, in DE 3235476 A1 and DE 102009029706 A1.
[0008] Regardless of the manufacturing method, the closure of the container generally takes place by pressing and sealing the edges of packaging material, for example by ultrasound, by means of a sonotrode and an anvil. Other methods for closing the container are also known, for example electromagnetic induction or exposure to hot air together with compaction by mechanical pressure.
[0009] Dust in particular has been found to be responsible for germ contamination, so avoiding dust should take priority at all stages. This can take place by suctioning the dust during the manufacture of the packaging wrap and reducing the exposure times of the used cutting blades. Due to the cellulose fibers of used cardboard, however, open cutting edges remain always the "trouble spots" in packaging manufacturing. Productive suction installations, although remedial in most cases, nevertheless load the production process through high energy costs and noise emissions.
[0010] Aseptic packaging means a packaging in which a filling material, in particular food, is introduced under aseptic conditions. The filling machines used for this comprise an aseptic zone, a kind of clean room, in which sterile conditions, free of germs, reign, for which maintenance, the room is closed or for the most part closed except for some openings. The clean room atmosphere formed in it is also under overpressure, through the inlet of sterile air, so that no germ can penetrate from the outside. The packaging material is then transported continuously or discontinuously through the aseptic zone, being sterilized, dried, filled in one or more stages and closed, in successive stages. By machining stage, current machines according to the state of the art, for example a machine of the applicant's 24 series, allow, depending on the packaging format, a machining time of each of the sterilization stations or fill from about 0.6 seconds to about 0.85 seconds.
[0011] The edges of the packaging wrap are cut edges made of laminated material that is otherwise watertight and optionally also has an oxygen barrier. Therefore, there is a risk of the exchange of germs (microorganisms and spores) firstly in the edge area, as a result of which an increase in the germ load of the material can take place and finally contamination cannot be ruled out. of the product during the subsequent filling of the packaging or closing to give the finished container.
[0012] Closing a full container, open on one side, made of composite material poses the risk that, in particular during ultrasonic sealing, dust from the packaging material may be thrown from the open cutting edges and this may contaminate both the aseptic area of the filling machine as the open packages themselves. Vegetative microorganisms are understood to be unicellular organisms that can multiply by cell division, which are suitable for multiplying in the filling material ("product") of a container and in this respect changing the properties of the filling material. Furthermore, the term also encompasses the persistent forms of cellular organisms that can multiply, such as for example their spores.
[0013] These spores are in most cases very resistant to changes in the surrounding environmental conditions. When microorganisms do not find an environment for metabolism and / or for reproduction, some microorganisms have the possibility of becoming a spore stage.
[0014] More precisely, by the term microorganisms in the sense of the present application, eukaryotes and prokaryotes are understood, the eukaryotes having a real cell wall and comprising algae, protozoa, fungi and yeasts, whereas prokaryotes cover the group of bacteria (see "Bergey's Manual of Determinative Bacteriology", 8th edition, Baltimore: Williams & Wilkins, 1974).
[0015] In particular in the case of prokaryotes, forms of persistence are known, such as spores for example. These can be found multiplied for example also after heat and / or chemical treatments of raw materials for the manufacture of cardboard raw products precisely in these, since treatment methods of this type either destroy the form that can multiply of the microorganisms or well initiates the transition to spore form.
[0016] As a measure of the number or quantity of the microorganisms contained in a quantity of substance, (for example in the raw cardboard product mentioned), the person skilled in the art knows the expression "colony forming unit per gram" (CFU / g ). Unlike the direct counting of all microorganisms present with a suitable optical medium, the determination of the number of colony-forming units takes place through the directed multiplication of the divisible microorganisms present under suitable culture conditions. In general this occurs up to a colony size that can be counted with the naked eye. In this regard, the fact that exactly one colony is generated is generated from each of the microorganisms that can divide, under the conditions defined above. Individual cases, in which two CFUs are so close together that only a visible colony is formed from them, are then regularly neglected.
[0017] Typical determination procedures in Microbiology are regulated in the ISO 8784-1 of 2005 standard. A reduction in CFU / g is used by the person skilled in the art, therefore, as a measure of the effectiveness of a procedure for the reduction of germs and is often referred to as the sterilization rate. Derived from this, the sterility rate results that can be counted through the number of packages produced.
[0018] From DE 102011111 523 A1 it is already known to treat open cut edges at the top or bottom of a packaging shell of a packaging material by applying a treatment agent containing a sterilizing agent, the sterilizing agent remaining after the application on the cutting edges and penetrating the packaging material. The application takes place in each case by spraying from above, a plurality of packaging shells being folded and flat together. In this known method, the application of the treatment agent on the packaging wrap edges takes place in a specially constructed station in one or more separate process steps immediately before packaging of the packaging wraps in a cardboard box. This procedure is relatively expensive. There is also the danger that it is accidentally sprayed while passing through the container. Furthermore, it has been shown that the outer sides of the packaging wrappers can be rapidly affected. For example, the treating agent can undesirably act on the image printed on the outer side of the packaging wrap and damage it. It can also happen that two packaging wraps stick to each other after being removed from the carton and that, during further processing in the filling machine, can lead to production interruptions.
[0019] A method is described in which at least a part of the treatment agent is not applied directly to the cutting edges, but instead a treatment carrier takes place, which receives the treatment agent, so that an active atmosphere The sterilant that is then fitted acts on the open cutting edges of the packaging wrap, cut-out or web product and effects the desired sterilization.
[0020] In this regard, sterilization to a sufficient depth in the carton can be achieved without influencing the known and proven course of packaging manufacture. The "sufficient depth" is determined in this respect by the manufacturing process used in each case. If the formation of seams takes place by means of ultrasound, then sterilization must take place to about 2 to 3 mm in depth, to reliably rule out that, during the sealing process, contaminated dust is thrown from the open edge. If the seam is closed by means of microwave technology, a depth of a few tenths of a millimeter is also sufficient.
[0021] Preferably, the transfer of the treatment agent or at least a part of the treatment agent takes place indirectly by evaporation and subsequent absorption at the open edge (s).
[0022] For this, the set sterilizing active atmosphere can be separated from the environment by means of a container. In this connection, preferably at least parts of the container, preferably parts of the inner side, are moistened with treatment agent.
[0023] In a further configuration, the container is an outer carton that serves for the storage and / or transport of the packaging wrap (s), the cut-out (s) or the / of the roll (s). In this connection, according to a further configuration, at least sub-areas of an inner side of the outer carton are moistened with a treatment agent.
[0024] In exemplary manufacture of paper / plastic composite packaging material, a carrier layer, generally paper or cardboard, is first coated and the composite material is produced in this manner. The composite material is then embossed before the crease and crease lines are introduced. After these processing steps, the web material is generally available as a product roll and can be further processed. However, prior to treatment according to the described method, preferably first, in a further working step, a cutout of the web material is perforated and laminated into stacks. From these cut-outs, packaging casings open at the top and bottom can then be generated by folding and connecting the side cutting edges (longitudinal seam sealing), which can then be sent to the bottling plants folded and packed flat. . Preferably, the process is carried out in connection with the packaging of the packaging casings and is thus not carried out in the aseptic zone of a filling machine, but rather outside the filling machine. In the event that the packaging wraps or blanks should be manufactured from a web product rolled into a roll, the method may be employed prior to cutting individual blanks to size, namely if the flat front surfaces of the cylindrical roll, which each consisting entirely of an open cutting edge, they are sterilized accordingly.
[0025] In the case where the packages are produced directly from a rolled web product, the front surfaces of the cylindrical roll, each consisting entirely of an open cutting edge, can be correspondingly sterilized.
[0026] It is convenient to provide an incubation time for the sterilizing agent. This is usually in the range of a few minutes to several hours and is sufficient to ensure disinfection of the edges throughout the transport time of the trimmings, packaging wraps or rolled web product to a filling machine. As a general rule, the treatment agent remains permanently in the packaging material. The edge areas of the scrap, packaging wrap or rolled web product remain germ-free for many days to a few months.
[0027] Starting from this, the invention is based on the objective of providing a particularly resource-friendly composite packaging and a packaging material necessary for this.
[0028] Regarding a packaging material and a packaging, in particular aseptic, formed from it, the object of the invention is achieved by the fact that the first sub-zone has a load of at least 100 colony-forming units per gram of cellulose / cardboard of microorganisms or spores, because at least one of the second subzones is delimited by an open cut edge or by drilling edges, the at least second subzone presenting, compared to the first subzone, a load of at most half of colony-forming units per gram of cellulose / cardboard of microorganisms or spores, and because a layer of cellulose / cardboard is hydrophilic and has a relative humidity of approximately 5.5% - 8.5%.
[0029] For a more detailed definition of the characteristics mentioned, reference is made to the more detailed explanation below of the determination method established in this case.
[0030] By designing a packaging material with the characteristics according to the invention, it is possible to be able to generate high-quality composite packages that safely protect the filling materials contained therein for a long period of time without having to depend on the material compound has to accumulate in a cellulose / cardboard stratum, presenting a loading of less than 100 CFU / g. Furthermore, it is therefore possible to significantly improve the environmental balance of a composite packaging model. Due to the lower demands of the cellulose / board stratum in terms of its microbial load, board grades that are manufactured with considerably less use of chemicals can be processed.
[0031] In this connection, in a special configuration of the invention, the first sub-zone even has a load of at least 250 CFU / g, preferably at least 500 CFU / g, more preferably at least 1000 CFU / g.
[0032] In this way, the environment is especially taken care of, since the manufacturing process of the usual special cardboard types for beverage boxes is indicated to a considerable extent for the use of polluting chemical products and also the energy demand is high compared to a conventional cardboard manufacture.
[0033] At least one open cutting edge of the respective packaging envelopes has been sufficiently penetrated by the sterilizing agent. This means that the edge areas located on the cutting edges and the edge areas which form at least one second sub-area are reduced to a sufficiently low germ load of at most half.
[0034] The edge zone of a cutting edge is understood to be those zones that are in contact with an open edge or are delimited by an open edge, an edge zone must have at least 0.3 millimeters deep and preferably must have at least 1 , 5 millimeters deep. In order to be able to discard in a particularly safe way contamination of food placed in an aseptic container, it is even preferred that the edge area is up to 2 millimeters thick, preferably even up to 3 millimeters or even up to 5 millimeters thick.
[0035] The area ratio between the first and the at least one second sub-area or in the case of several second sub-areas, the total area of the second sub-areas is preferably from about 8: 1 to about 60: 1. In this regard, the at least one second sub-area always forms a defined shape, preferably an annular surface or a strip shape. The size of the surface depends on the format of the composite (rear) packaging and the width of the edge area that forms the at least one second sub-area, thus, on the penetration depth of the treatment agent (measured from the cutting edge to inside the surface of the packaging material).
[0036] With respect to a given package format or a given type of packaging, the distribution between the first and the at least one second sub-zone forms a repeating pattern. This means that the first and at least one second sub-zone in particular are not randomly distributed in the processing of a bundle, but rather follow a repeating pattern related to type. For example, the surface of a processed composite package can form a rectangle. Except for a single second sub-area, which is formed by an edge area running along one of the four edges, the surface may be filled from the first sub-area. If two second sub-areas are provided for the corresponding type of composite package, these can be formed by edge areas at edges that are opposite each other or that abut each other at right angles. It is also conceivable that the four edge areas delimited by a respective edge form a second sub-area and thus completely frame the first sub-area. If a perforation, for example circular, is provided within the surface formed by the first sub-zone, it is conceivable that a second annular sub-zone limits as an edge zone on or around the edge formed by the perforation. The stratum of this second subzone also repeats regularly within the series of one type of composite pack. Another teaching of the invention provides that the at least one cellulose / cardboard layer has portions of recycled fibers.
[0037] For sensitive applications, for example food packaging, cardboard webs with portions of recycled fibers have not been considered until now, because these webs can exhibit indefinable qualities and amounts of fouling or contamination. By using the process or product, these are ecologically useful and can be practically used worldwide to a sufficient degree and the available resources can also be used for the first time for the protection of foods to be aseptically packed, in particular so the so-called UHT milk.
[0038] Another configuration of the invention provides that the second sub-zone has, compared to the first sub-zone, a load of at most one quarter, preferably one tenth, more preferably one hundredth, of colony-forming units per gram of cellulose / cardboard. . It is even possible that the loading of colony forming units per gram of cellulose / board can take on significantly smaller fractions. Therefore, the risk of contamination of the filling products is further reduced.
[0039] According to a further embodiment of the invention, the edge areas on the cutting edges have a maximum of 10 CFU / g, preferably a maximum of 5 CFU / g and more preferably less than 1 CFU / g. Therefore, extremely good sterilization rates can be achieved. Other than that, particularly in In the case of compounds without aluminum, the useful life of the finished package and the filling products to be protected can also be increased.
[0040] According to the invention, at least one of the second sub-areas is delimited by an open cutting edge or by perforation edges. Preferably, the "edge zone" which occurs along the open cutting edges or perforation edges, which is impregnated with the sterilizing agent, is configured to be at least 0.3 mm thick, in particular 1 , 5 mm thick and particularly preferably at least 2 mm thick.
[0041] In this respect, the second sub-area is preferably delimited in comparison with the first sub-area by an imaginary line which runs essentially parallel to the cutting or drilling edge delimiting the second sub-area.
[0042] Preferably, the transmission of the treatment agent takes place indirectly by evaporation and subsequent absorption at the open cutting edge (s) of the packaging material. For this, in particular at least partial areas of the inner side of a container, in particular of an outer carton, are moistened with treatment agent or, however, support elements are used to be inserted or to be removed. to stick in the container as load carriers.
[0043] Loading of all or selected parts of the inner side of the container, in particular of an outer packaging (outer carton or inserted or glued load carrier), with treatment agents, in particular thus a sterilization solution, can be carried out before or after closing the container. The method before closing is preferred.
[0044] In the case of the container, if it is a corrugated cardboard outer carton, it offers the advantage that the absorption of the sterilizing agent by the loaded outer carton flaps takes place in the outer carton along the edges. Top or bottom open side surface cartons of the packaged side surfaces. In contrast to a sterilization of the side surfaces of the package according to DE 102011111 523 A1, the workload, which has already been significantly reduced in any case, can be reduced once again in this respect if the treatment agent is applied to the outer carton packaging outside the direct production line, for example in an adjacent room. In this connection, in some cases, it may even be particularly preferred if the outer carton, for its part present as a folding box, is loaded already before or during unfolding of the outer carton. It is possible to "inoculate" the atmosphere of the container, preferably enclosed by the outer carton, after closing the carton, for example, with a needle, the outer carton having to be pierced once or several times in suitable places, for example For example, in the upper free space. Furthermore, it is conceivable that a load carrier, for example a felt strip, is applied to the inner side of the outer carton before closing and after closing the outer carton it is penetrated with a needle so that the needle You can inject the treatment agent into the load carrier. In this way, the environment is practically unaffected by the active principles contained in the treatment agent.
[0045] To this end, in a further configuration, the container can also comprise a valve. The use of a valve effectively prevents the treatment agent from escaping from the container or from diffusing too much. The valve can be designed as a mechanical one-way valve or as a pierceable and self-closing diaphragm. The provision of a mechanical valve can be particularly advantageous in the case of reusable containers, while a self-closing membrane can also very easily be attached to the container from the outside or the inside and offers sufficient protection at least for a single use.
[0046] Preferably, the treating agent is colored with a suitable colorant. Therefore, the mounting area can be easily determined visually. This can serve for control purposes. If, apart from that, a colorant is used which, together with the sterilizing agent, is absorbed from the open cutting edges of the packaging material from the active sterilizing atmosphere, a treatment carried out can also be verified on the packaging material by a simple visual check. In this case, the depth of penetration of the treatment agent in the edge region can also be recognized. Thus, it is preferable that the dye causes discoloration of the treated edges. A further teaching of the invention provides that the composite package according to the invention is produced from the packaging material according to claims 1 to 7. A load of an outer packaging at a suitable point, for example, the inner sides of the flaps of an outer carton, with a treatment agent containing a sterilizing agent, for example, a peroxide solution, can be made by spraying, dripping and spreading, coating, roll coating, wiping, coating with spatula, stamping (for example, with an "inkjet" process), dipping or steaming. As already mentioned, the loading can also be carried out as an injection. The sterilizing agent can also be applied to the edges of packaging materials to be transported in a container by attaching a strip, insert sheet, or other carrier material loaded with a sterilizing agent.
[0047] In this regard, it may be advantageous if the charge carrier is configured as an accumulator and can be filled with a liquid treatment agent in order to release the treatment agent back into the environment. Porous or cellular storage materials are particularly suitable for this.
[0048] Flat-folded packaging materials packed in a container, in particular an outer carton, are generally transported over a period of several days. Meanwhile, a germ reduction or sterilization of the open cardboard edges and of the container or outer packaging takes place by the absorbed sterilizing agent. In this regard, surprisingly, it has been found that despite very low concentrations of the sterilizing agent, first-rate sterilization rates occur. It is now assumed that the low concentrations of the sterilizing agent can take advantage of the long residence time in the container as an effective exposure time. The active sterilization atmosphere that is set can thus be kept in an effective setting for a long period of several hours or even days. Thus, a long exposure time occurs with low concentration. In this regard, depending on the amount used, the sterilizing agent penetrates up to 2mm or 3mm or even deeper into the edge region or the perforation region of the cardboard. This is important, because the fibers located there in the cellulose / cardboard layer cannot be called stationary and, as a result, the germs located in the fibers are not bound, but can escape with the dust fibers of the cellulose / cardboard layer .
[0049] The action time depends, in each case with respect to a given cardboard grammage and type, the treatment agent used or the additives contained, the dosage, the expected sterilization rate and the ambient temperature.
[0050] An absorption of treatment agent through the cardboard edge is possible, since the cardboard used for the packages to be manufactured is hydrophilic, and in general, as a finished product, has a relative humidity of approximately 5.5% - 8.5%, that is, the humidity of the cardboard is well below the saturation limit resulting from the prevailing environmental conditions and is identical to the equilibrium humidity with the environment.
[0051] The addition of a polar organic solvent exhibiting a lower vapor pressure than the active agent, that is to say in this case the sterilizing agent, acts as an accelerator in this case. Thus, the addition of ethanol to, for example, a peroxide solution enhances the absorbent effect of the cutting edge and increases the penetration of the peroxide into the cardboard. This allows a deeper filtration of the sterilizing agent at the cutting edges, so that with a suitable ratio of sterilizing agent and ethanol, even after a few hours, an edge area of the packaging material can be sterilized. to be treated up to several millimeters.
[0052] Ethanol belongs to the group of polar organic solvents that generally act as accelerators when their vapor pressure is lower than that of the active medium. If the vapor pressure of the added polar organic solvent is greater than that of the active agent, the solvent acts as a retarder. An example of a solvent with a higher vapor pressure is DOWANOL®, a commercial product from the DOW Chemical Company. In general, it can be said that low molecular weight polar organic solvents have low vapor pressure and high molecular weight organic solvents have high vapor pressure.
[0053] Additionally, the sterilizing effect of some sterilizing agents is synergistically enhanced.
[0054] Determination method:
[0055] For a more detailed definition of the characteristics mentioned in the claims, the following determination method is established:
[0056] Determination of colony forming units per gram ( CFU / g)
[0057] The European standard method ISO 8784-1: 2005 and the references cited in these test instructions are selected as the basis for the determination of colony forming units per gram (CFU / g). The test instructions are used in this case to examine the loading per CFU / g of packaging material or composite material of cardboard, plastic and partly aluminum. If deviations from the above test instructions are necessary when carrying out the sampling and determination of the CFU / g of the packaging material, then they are explained below.
[0058] 1.1.1. Sampling and sample preparation
[0059] Samples of packaging material taken cannot be taken by hand. Storage occurs in sterile collection containers, preferably sterile plastic bags. The areas to be examined are cut into pieces with sterile scissors.
[0060] "Area to be examined" is:
[0061] to. The first sub-zone, according to claim 10, which is not an edge zone (sampling at least 10 millimeters away from the open cutting edge)
[0062] b. The second sub-zone or edge zone, according to claim 10, on the open cut edges or the perforation edges of the packaging material (up to a maximum of three millimeters from the open cut edge).
[0063] As a complement to the European standard method ISO 8784-1: 2005, chapter 8 “Preparation of the test material”, a maximum of 3 g of packaging material is used for the first sub-zones. For the second, a maximum of 3 g of packaging material is also used. If not enough material is obtained from a sample fragment, then the second sub-areas of a maximum of 5 identical sample fragments are used together.
[0064] 1.2. Optional determination of the number of surface germs
[0065] There is the possibility that the packaging material samples are contaminated prior to sampling as well as the presence of germs inside, also superficially. An error in the determination of the CFU / g of the packaging material can be prevented by determining the number of surface germs and the number of surface germs is subtracted from the numerical value determined in 1.1. of colony-forming units per gram.
[0066] 1.2.1. Terms and abbreviations
[0067] ml = milliliter
[0068] h = hour
[0069] CFU = colony forming units
[0070] ° C = degree Celsius
[0071] g = gram
[0072] mm = millimeter
[0073] cm = centimeter
[0074] 1.2.2. Required auxiliary means
[0075] Contact Petri dishes (plastic) 05.5 cm (for example Greiner Bio-one 629180) forceps
[0076] Cutter-blade
[0077] Sterile foil bags or aluminum foil
[0078] Sterilizer
[0079] Growing stove
[0080] sterile workbench
[0081] nutrient media: Plate-Count-Agar (for example available as Oxoid # CM 325, Merck # 105463, Difco # 247940)
[0082] 1.2.3. Realization
[0083] 240 cm2 of surface area of packaging material is examined per sample.
[0084] A contact Petri dish has a surface area of 24 cm2. Therefore 10 contact plates per sample have to be prepared to examine the aforementioned surface.
[0085] A quantity of culture medium is added to the sterile Petri dishes such that the agar protrudes above the edge of the Petri dish (curvature), but does not spill over the edge. The prepared cooled contact plates are pressed onto the surface of the packaging material, closed and incubated under the indicated conditions.
[0086] Care must be taken that the sample fragments are touched only with sterile forceps and that the contact plates do not come into contact with the open container edge.
[0087] Petri dishes are placed with the lid down in the culture oven to avoid the formation of condensed water.
[0088] Culture medium: Plate-Count-Agar is used for the number of germs on the surface.
[0089] Incubation: _Incubation of Plate-Count-Agar takes place for 5 days at 30 ° C, with evaluation taking place thereafter.
[0090] 1.2.4. Evaluation
[0091] All colonies on the contact plates of a sample are counted. Results are converted to CFU (colony forming units) / 100 cm2 and documented. The value obtained is converted into the area of the areas to be examined and is subtracted as a numerical value from the value of the colony forming units per gram.
[0092] Examples:
[0093] For the implementation of the process according to the invention, for example, a hydrogen peroxide solution from 3.5% to 50% with or without the addition of
[0094] - evaporation retarder (for example DOWANOL®)
[0095] - agents that reduce surface tension, such as, for example, parts of alcohol (parts of alcohol with retarding agents, surface-active substances such as surfactants, etc.)
[0096] - peracetic acid 3-15%
[0097] - n- or isopropanol
[0098] - other agents with sporicidal action.
[0099] The solution can be treated in a mixture with water or alcohol (ethanol), this can be completely volatilized without toxic residues. Of course, the treatment agent may also have another suitable sterilizing agent as a substitute for the hydrogen peroxide solution.
[0100] Table 1 shows 12 application examples. The following fundamental conditions apply to these Examples:
[0101] The evaluation of the CFU / g took place according to the norms and procedures described in the methods. The treated packaging material has as a cardboard layer a cardboard from the company Stora Enso Natura Board with a grammage of 230 g / m2. When not described otherwise, 350 packaging walls were preserved in one container. Containers have the following properties:
[0102] Cardboard box: container made of corrugated cardboard with dimensions width: 60 cm; height: 19 cm; depth: 10.5 cm
[0103] Plastic box: container made of polypropylene with lid with dimensions width: 60 cm; height: 19 cm; depth: 10.5 cm
[0104] Shrink sheet: sheet made of polyolefins with the dimensions width: 1 m; length: 2.5 m; thickness: 20 | jm
[0105] Loaded paper support: DIN A4, cellulose weighing 150 g / m2
[0106] The treatment agent results from the following chemicals:
[0107] H O Solution: Peroxal DS, 35% H2O2 Solution (Food Grade)
[0108] Ethanol: Technical ethanol (99%) denatured with MEK (1%)
[0109] Methanol: Technical methanol (98%)
[0110] Dowanol: 1-Methoxy-propanol-2 from the company Dow
[0111]
[0112] L n:
[0116] In summary, the advantages of the described procedure can be described with the following keywords:
[0117] - treatment agent can be applied in a defined way on the cardboard box flaps.
[0118] - Minimal consumption of sterilizing agent compared to direct spraying of the edges. This clearly reduces the potential for risk and contamination to the working environment.
[0119] - Overloading by direct spray application is avoided.
[0120] - The time until the absorption exchange between the cardboard flap / wall edge or perforation is sufficiently present by means of the transport from the production site to the bottling company (frequently greater than 3 days).
[0121] - The color characterization of the treatment agent on the cardboard box flaps is useful, therefore suitable application and dosage controls are possible.
[0122] - Due to minimal absorption amounts, no detectable residual amounts of sterilizing agent are present, for example residual amounts of peroxide before processing of the packaging material in the filling machine. A health risk is therefore ruled out.
[0123] - No influence from the visible area on the outside of the packaging. In particular, the sales-important printed image of the composite packaging is not attacked, and adjacent packaging wrappers are effectively prevented from sticking together in the feeding process of a filling machine.
[0124] - The treatment agent, in particular the peroxide solution, acts practically exclusively on the open cutting edges, because it is actively absorbed by them. No contamination of the rest of the container.
[0125] The invention is explained in detail below by means of a drawing which describes only exemplary embodiments. In the drawing they show
[0126] Figure 1A a cutout for beverage boxes in top view,
[0127] Figure 1B flat-folded packaging wrap, produced from a cutout according to Figure 1A,
[0128] FIG. 2 a cardboard box for housing a plurality of packaging envelopes with box flaps open at the top in vertical section,
[0129] Figure 3 shows a first embodiment of a cardboard box that is open at the top with flat-folded packaging envelopes that are therein in perspective representation, Figure 4 a second embodiment of a cardboard box that is open at the top with flat-folded packaging wraps located therein in perspective representation, Figure 5 another embodiment of a cardboard box open at the top with flat-folded packaging wraps located therein in perspective view ,
[0130] Figure 6 another example of embodiment of a container in vertical section,
[0131] Figure 7 shows a container to house a roll of packaging material in vertical section and
[0132] Figure 8 shows a corner section of a container with a support element fixed inside.
[0133] In Figure 1A, cutout B produced from a composite laminated material is represented, which presents, above, below and on its right side, three zones 1, 2, 3 for the subsequent production of seams and is also provided with a plurality of grooving and folding lines 4, which facilitate the subsequent unfolding of the finished beverage box and of which only some have been provided in Figure 1A with the reference number 4. A perforation can be seen on the upper side of cutout B round P as a zone of weakness for a filling element to be applied (not shown).
[0134] In Figure 1B a packaging casing S produced from a cut-out B according to Figure 1A is represented, in which the cut-out B was joined in its seam area 3 with a sleeve by sealing a longitudinal seam 6 and it was folded flat with a packaging wrap S. The flat folding takes place for a simple reason, since as a rule the manufacturing of the packaging wraps S takes place in a place other than the subsequent further processing into beverage containers , which takes place in bottling companies in different locations. For this purpose, a plurality of vertically flat folded packaging envelopes S are packed in so-called cardboard boxes 7 and transported to the respective company. The residence time of the packaging wraps S on the cardboard boxes 7 until their opening immediately before the filling machine amounts in most cases to clearly more than three days.
[0135] It has proven to be advantageous that the open container edges which are problematic in terms of contamination are no longer loaded directly with a sterilizing agent on the lower or upper side of the packaging casings S, but such that at least a part of the treatment agent which present the sterilizing agent is applied to a support element, so that the set sterilizing active atmosphere then acts on the open cutting edges and effects the desired sterilization of the edge zones 5 of the edges or annular zones 5 ' of the packaging envelopes S. As a support element a corrugated cardboard box 7 can preferably be used in which the upper and lower flaps 8A and 8B, 8A 'and 8B' are moistened on the inside of the box with a treatment agent, specifically in the area of the arrows not designated in detail in Figure 2.
[0136] In this way, a sterilizing active atmosphere is set in the closed cardboard box 7 in which the treatment agent can penetrate the open cutting edges of the packaging envelopes S, or in which the cardboard material in the region edge or perforation sealed to open cutting edges is encouraged to absorb treatment agent. There, the sterilizing agent penetrates to a degree (a few millimeters) into the cardboard material such that sufficient sterilization is achieved.
[0137] However, it is also possible that the treatment agent is not applied directly to the surface of the carton 7, but is applied there with the aid of a load carrier or carrier element. For this, for example, only strips 9, as shown in Figure 3, of adhesive tape, felt or other suitable materials can be placed, which are glued on the inside of the cardboard box 7 or in the lower area of the box. cardboard 7. It has been shown that a complete wetting is not necessarily necessary to obtain a sufficient saturation of the atmosphere with a sterilizing agent.
[0138] Figure 4 now shows that it is also possible to place a loose sheet 10 in the cardboard box 7 (below and / or above), the loose sheet 10 having been moistened over its entire surface or also only partially with the necessary amount of agent. treatment.
[0139] In FIG. 5 it is shown that it is also possible to provide a loose sheet 11 with strip-shaped load carriers 12, which is then placed in reverse on the upper open cutting edges of the packaging casings S, before the cardboard box 7 can of course also be placed before the packaging envelopes S are inserted into the cardboard box 7 a correspondingly prepared single sheet on the bottom of the cardboard box 7, to also sterilize the edges lower open cutting edges of the packaging wrappers S.
[0140] In Figure 6 it is seen that the vertical flat folded packaging wraps S can also be transported in an "outer packaging" of a plastic material. A plastic container 13 is clearly seen in vertical section on which a corresponding lid 14 is placed. In the headspace of this outer packaging 7 'a prepared loose sheet 11' is placed which serves as a load carrier, to achieve the necessary sterile atmosphere. For the best closure, the "open" transitions between container 13 and lid 14 can also be closed with an adhesive tape.
[0141] It is not represented that it is also possible to provide not a plurality of vertical and flat-folded packaging wraps with a fixed outer packaging, but for example to surround them with a shrink sheet, previously placing a corresponding intermediate piece of support material on the area of the open cutting edges, to carry out the desired sterilization there.
[0142] Figure 7 shows that it is also possible to treat a roll R wound on a sleeve T of a composite packaging material at its open edges with the method according to the invention. This is advantageous in particular when the width of the roll corresponds exactly to the height of the package, because then both circular surfaces of the roll consist of cutting edges that are open almost over the entire surface. To this end, the roll R, in the illustrated embodiment and in this preferred sense, is surrounded by a two-part shrink cover consisting of a smaller cover part 15 and a larger cover part adapted to the same 16. It is It also recognizes in this case that inserted blades 11 "are present in the area of the open cutting edges to create the desired sterile atmosphere. It is of course also possible in the case of roll material packaging to pack this in shrink foil, as described above, after providing it with load carriers 11 ".
[0143] In Figure 8 it is now represented in the example of the upper left corner of the container of Figure 6, that it is also possible to introduce as a load carrier a somewhat bulky strip 17 of felt material or the like, in this case a loading of strip 17 with treatment agent also after closure of the container. To do this, a needle is pierced through a wall of the container and in this way the strips 17 located inside are soaked with the necessary amount of treatment agent to sufficiently sterilize the flat-folded packaging envelopes S, already finished packaging, in its open cutting edges. For For this, the container can have a prepared channel opening 18. It is also possible, if necessary, that additional strips 17 'can be provided as load carriers in the head space of the container.
权利要求:
Claims (8)
[1]
1. Packaging material, in particular packaging wrap (S), cut-out (B) or a web product rolled into a roll (R) for the manufacture of packaging, in particular aseptic, consisting mainly of a composite material with at least one cellulose / cardboard layer, the at least one cellulose / cardboard layer presenting a first sub-zone and presenting at least one second sub-zone, and the at least one second sub-zone presenting, compared to the first sub-zone, a load of as maximum half of colony forming units per gram of cellulose / cardboard of microorganisms or spores,
characterized by what
the first sub-zone has a load of at least 100 colony-forming units per gram of cellulose / cardboard of microorganisms or spores, because at least one of the second sub-zones is delimited by an open cut edge or by perforation edges, and by that a cellulose / cardboard sheet is hydrophilic and has a relative humidity of approximately 5.5% - 8.5%.
[2]
2. Packaging material according to claim 1,
characterized by what
the first sub-zone has a loading of at least 250 CFU / g, preferably of at least 500 CFU / g, more preferably of at least 1000 CFU / g.
[3]
3. Packaging material according to claims 1 or 2,
characterized by what
The at least one cellulose / cardboard layer has portions of recycled fibers.
[4]
Packaging material according to one of claims 1 to 3,
characterized by what
the second sub-zone has, compared to the first sub-zone, a loading of at most one fourth, preferably one tenth, more preferably one hundredth, of colony-forming units per gram of cellulose / cardboard.
[5]
Packaging material according to one of claims 1 to 4,
characterized by what
the edge areas (5, 5 ') located on the cutting edges have a maximum of 10 CFU / g, preferably a maximum of 5 CFU / g and more preferably less than 1 CFU / g.
[6]
Packaging material according to one of Claims 1 to 5,
characterized by what
the at least one second sub-zone is formed by an edge zone.
[7]
7. Packaging material according to claim 6,
characterized by what
the edge region (5 or 5 ') is configured to be at least 0.3 mm thick, in particular at least 1.5 mm thick, more preferably at least 2 mm thick.
[8]
8. Composite packaging, in particular aseptic composite packaging,
characterized by what
It is made from the packaging material according to claims 1 to 7.
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同族专利:
公开号 | 公开日
JP2017507854A|2017-03-23|
US20160332795A1|2016-11-17|
ES2772757T3|2020-07-08|
EP3251958A3|2018-03-14|
US20190144192A1|2019-05-16|
JP6563403B2|2019-08-21|
RU2016132624A|2018-02-14|
US20200255205A1|2020-08-13|
US10696465B2|2020-06-30|
EP3092175B1|2017-12-27|
AU2015205693A2|2016-08-04|
ES2658296T3|2018-03-09|
WO2015104234A1|2015-07-16|
EP3251958A2|2017-12-06|
EP3092175A1|2016-11-16|
CN105939935B|2020-03-13|
RU2016132624A3|2018-07-13|
EP3251958B1|2020-01-29|
EP3251958B9|2020-11-04|
PL3251958T3|2020-05-18|
CN111498174A|2020-08-07|
CN105939935A|2016-09-14|
MX2016008564A|2016-10-03|
DE102014100203A1|2015-07-09|
US10207852B2|2019-02-19|
DE102014100203A9|2015-11-12|
EP3461750A1|2019-04-03|
PL3092175T3|2018-04-30|
AU2015205693A1|2016-07-14|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题

US4061785A|1969-04-26|1977-12-06|Tetsuya Nishino|Method and device for preserving vegetables|
DE3235476C2|1981-11-14|1986-09-11|Jagenberg AG, 4000 Düsseldorf|Method and device for disinfecting packaging material, in particular packaging containers|
BE894957A|1981-11-14|1983-03-01|Jagenberg Ag|METHOD AND DEVICE FOR STERILIZING PACKAGING MATERIAL, IN PARTICULAR, PACKAGING CONTAINERS|
DE3207426C2|1982-03-02|1985-04-04|Hassia Verpackungsmaschinen GmbH, 6479 Ranstadt|Device for the production of containers from thermoplastic film strips|
JPS6080456A|1983-10-12|1985-05-08|Mitsuru Tsuchikura|Deodorant pasturizer mounted in package and corrugated boardbox|
JPH0356222A|1989-07-26|1991-03-11|Toyo Seikan Kaisha Ltd|Dry sterilizing method for germfree filling container|
AU1357097A|1996-02-27|1997-09-16|Tetra Laval Holdings & Finance Sa|Process for sanitizing post-consumer paper fibers and product formed therefrom|
SE511348C2|1996-11-01|1999-09-13|Tetra Laval Holdings & Finance|Collection box with packaging container blanks|
EP1332969B1|2000-07-31|2012-01-18|Tetra Laval Holdings & Finance SA|Method of manufacturing paper packaging container, paper packaging container andweb-shaped packaging material|
CN101014318A|2004-05-03|2007-08-08|威尼特·尚塔拉特|Cleansing and rinse solutions for skin and hair and method of using|
NZ543085A|2005-10-20|2008-03-28|Mercer Technologies Ltd|Method and apparatus for sterilization and vacuum packing in a hospital, laboratory or food processing environment|
DE102009029706A1|2009-06-08|2010-12-09|Sig Technology Ag|Method and device for sterilizing packaging|
DE102011111523B8|2011-08-31|2013-03-28|Sig Technology Ag|Method and device for edge sterilization of packaging material|
US9078435B2|2011-09-08|2015-07-14|Joseph Dunn|Methods for disinfecting or sterilizing articles|GB201205243D0|2012-03-26|2012-05-09|Kraft Foods R & D Inc|Packaging and method of opening|
GB2511559B|2013-03-07|2018-11-14|Mondelez Uk R&D Ltd|Improved Packaging and Method of Forming Packaging|
GB2511560B|2013-03-07|2018-11-14|Mondelez Uk R&D Ltd|Improved Packaging and Method of Forming Packaging|
DE102016209236A1|2016-05-27|2017-11-30|Sig Technology Ag|Method for producing a packaging enveloping container precursor, in particular for a single dimensionally stable food container, with folding over the container precursor|
DE102017131262A1|2017-12-22|2019-07-11|Sig Technology Ag|Container made of packing coats and an outer packaging|
JP6583467B1|2018-03-29|2019-10-02|大日本印刷株式会社|Aseptic filling machine paper container sterilization method|
DE102019110620A1|2019-04-24|2020-10-29|Sig Technology Ag|System for packing several containers on one plate|
WO2021035326A2|2019-08-28|2021-03-04|Shandong Bihai Packaging Materials Co. Ltd.|Processes and equipment to manufacture aseptic carton packages provided with longitudinal joining and sealing side regions and process to manufacture multilayer laminated packaging material used to produce said aseptic carton packages provided with longitudinal joining and sealing side regions|
US20210339519A1|2020-04-30|2021-11-04|Sergio Ribeiro Romeiro|Process to manufacture multilayer laminated packaging material|
法律状态:
优先权:
申请号 | 申请日 | 专利标题
DE102014100203.2A|DE102014100203A1|2014-01-09|2014-01-09|Process for treating the open cut edges of packaging material for the manufacture of cardboard / plastic composite packaging and a packaging material, a composite package produced therefrom and a container for receiving packaging material|
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