WO2022059592A1 - 積層体及び成形体 - Google Patents

積層体及び成形体 Download PDF

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Publication number
WO2022059592A1
WO2022059592A1 PCT/JP2021/033162 JP2021033162W WO2022059592A1 WO 2022059592 A1 WO2022059592 A1 WO 2022059592A1 JP 2021033162 W JP2021033162 W JP 2021033162W WO 2022059592 A1 WO2022059592 A1 WO 2022059592A1
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Prior art keywords
hydroxybutyrate
poly
resin
coating layer
p3hb
Prior art date
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Ceased
Application number
PCT/JP2021/033162
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English (en)
French (fr)
Japanese (ja)
Inventor
明日香 福留
康則 岡田
徹雄 大倉
健介 村島
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Kaneka Corp
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Kaneka Corp
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Filing date
Publication date
Application filed by Kaneka Corp filed Critical Kaneka Corp
Priority to CN202180063468.3A priority Critical patent/CN116940467B/zh
Priority to EP21869279.6A priority patent/EP4215366A4/en
Priority to US18/245,596 priority patent/US12540438B2/en
Priority to JP2022550510A priority patent/JP7771070B2/ja
Publication of WO2022059592A1 publication Critical patent/WO2022059592A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00—Coated paper; Coating material
    • D21H19/02—Metal coatings
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/10—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of paper or cardboard
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04—Interconnection of layers
    • B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00—Coated paper; Coating material
    • D21H19/10—Coatings without pigments
    • D21H19/12—Coatings without pigments applied as a solution using water as the only solvent, e.g. in the presence of acid or alkaline compounds
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00—Coated paper; Coating material
    • D21H19/10—Coatings without pigments
    • D21H19/14—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/24—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H19/28—Polyesters
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/18—Reinforcing agents
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H25/00—After-treatment of paper not provided for in groups D21H17/00 - D21H23/00
    • D21H25/04—Physical treatment, e.g. heating, irradiating
    • D21H25/06—Physical treatment, e.g. heating, irradiating of impregnated or coated paper
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
    • D21H27/10—Packing paper

Definitions

  • the base material layer may be subjected to surface treatment such as corona treatment, frame treatment, and anchor coating treatment. These surface treatments may be performed alone or in combination of a plurality of surface treatments.
  • the coating layer can be formed by applying an aqueous coating liquid to one side or both sides of the base material layer, heating, drying and forming a film. Therefore, when the coating layer is directly laminated on the base material layer without interposing another layer, a part of the aqueous coating liquid permeates the base material layer in the manufacturing process of the laminated body, and the coating layer and the base material layer are laminated.
  • An intermediate layer containing a part of the poly (3-hydroxybutyrate) resin derived from the coating layer and a part of the base material derived from the base material layer can be formed between the two.
  • the coating layer contains at least a poly (3-hydroxybutyrate) resin.
  • the poly (3-hydroxybutyrate) -based resin (hereinafter, also referred to as P3HB-based resin) is an aliphatic polyester resin that can be produced from a microorganism and has 3-hydroxybutyrate as a repeating unit.
  • the P3HB-based resin may be a poly (3-hydroxybutyrate) having only 3-hydroxybutyrate as a repeating unit, or a copolymer of 3-hydroxybutyrate and another hydroxyalkanoate. May be good.
  • the P3HB-based resin may be a mixture of a homopolymer and one or more types of copolymers, or may be a mixture of two or more types of copolymers.
  • the type of copolymerization is not particularly limited, and may be random copolymerization, alternate copolymerization, block copolymerization, graft copolymerization, or the like.
  • P3HB resin examples include poly (3-hydroxybutyrate) (P3HB), poly (3-hydroxybutyrate-co-3-hydroxyhexanoate) (P3HB3HH), and poly (3-hydroxybutyrate-co).
  • -3-Hydroxyvariate) P3HB3HV
  • Poly (3-hydroxybutyrate-co-3-hydroxydecanoate) P3HB3HD
  • Poly (3-hydroxy) Butyrate-co-3-hydroxyvariate-co-3-hydroxyhexanoate) P3HB3HV3HH
  • the melting point and the crystallinity can be changed, and as a result, the physical properties such as the Young rate and the heat resistance can be changed, and the physical properties between polypropylene and polyethylene can be changed.
  • a copolymer of 3-hydroxybutyric acid and 3-hydroxyhexanoic acid from the viewpoint of being able to be imparted and being a plastic that is industrially easy to produce and is physically useful as described above.
  • Certain P3HB3HH is more preferred. Further, P3HB3HH is preferable from the viewpoint that the melting point can be lowered and the molding process at a low temperature becomes possible.
  • the P3HB-based resin preferably contains at least one type of P3HB3HH, and at least two types of poly (3-hydroxybutyrate-co-3-hydroxyhexa) having different content ratios of constituent monomers. Noate) is particularly preferred. It is also preferable to include at least one type of P3HB3HH and P3HB.
  • the microorganism that produces the P3HB-based resin is not particularly limited as long as it is a microorganism that has the ability to produce the P3HB-based resin.
  • a P3HB-producing bacterium Bacillus megaterium, which was discovered in 1925, is the first, and in addition, Cupriavidus necator (former classification: Alcaligenes europhos, Ralstonia eutropha). Examples include natural microorganisms such as Alcaligenes lattice. It is known that P3HB is accumulated in the cells of these microorganisms.
  • Microbial cells obtained by culturing these microorganisms under appropriate conditions and accumulating P3HB3HH in the cells are used.
  • a recombinant microorganism into which various P3HB resin synthesis-related genes have been introduced may be used according to the P3HB resin to be produced, or the culture conditions including the type of substrate may be optimized. good.
  • Microorganism-produced P3HB3HH is a random copolymer.
  • the adjustment of the 3HH unit content ratio can be performed by, for example, selection of bacterial cells, selection of a carbon source as a raw material, blending of P3HB3HH having different 3HH unit content ratios, blending of 3HB homopolymers, and the like.
  • the coating layer may contain one or more resins other than the P3HB resin as long as the effect of the invention is exhibited.
  • resins include aliphatic polyester resins such as polybutylene succinate, polycaprolactone and polylactic acid, and aliphatic polyester resins such as polybutylene adipate terephthalate, polybutylene succinate terephthalate and polybutylene azelate terephthalate.
  • aromatic polyester-based resins The amount of these resins added is preferably 10 parts by weight or less with respect to 100 parts by weight of the P3HB-based resin in order to ensure the biodegradability of the coating layer.
  • the coating layer does not have to contain a resin other than the P3HB-based resin.
  • the coating layer may contain additives usually used in the art as long as the effects of the invention are exhibited.
  • additives include inorganic fillers such as talc, calcium carbonate, mica, silica, titanium oxide, and alumina, used paper such as fir tree, wood flour, and newspaper, and organic fillers such as various starches and cellulose.
  • Colorants such as pigments and dyes, odor absorbers such as activated charcoal and zeolite, fragrances such as vanillin and dextrin, plasticizers, antioxidants, antioxidants, weather resistance improvers, ultraviolet absorbers, crystal nucleating agents, lubricants, etc.
  • the temperature difference between Tma and Tmb is 10 ° C. or higher, preferably 15 ° C. or higher, more preferably 20 ° C. or higher, still more preferably 25 ° C. or higher. If the temperature difference is less than 10 ° C., it may be difficult to achieve the effect that good adhesive strength can be exhibited in a short time after heating even if the resin is heated to a temperature at which it can be sufficiently adhered. be.
  • the upper limit of the temperature difference between Tma and Tmb is not particularly limited, but from the viewpoint of ease of production, it is, for example, 60 ° C. or lower, more preferably 50 ° C. or lower.
  • the peak top temperature of the crystal melting curve in the differential scanning calorimetry is defined as follows.
  • An aluminum pan is filled with 2 to 5 mg of a coating layer separated from the substrate layer, and the temperature is raised from 20 ° C. to 190 ° C. at a rate of 10 ° C./min under a nitrogen stream using a differential scanning calorimeter.
  • the coating layer is melted to obtain a crystal melting curve.
  • the top temperature of the melting point peak existing in the range of 100 to 150 ° C. is Tma
  • the top temperature of the melting point peak existing in the range of 150 to 170 ° C. is Tmb.
  • the total value of the crystal melting enthalpies of all the melting point peaks is set as ⁇ Ha, and multiple melting point peaks are found in the range of 150 to 170 ° C. If it is found, the total value of the crystal melting enthalpies of all those peaks shall be ⁇ Hb.
  • the weight (weight) per unit of the P3HB-based resin in the coating layer is preferably 5 to 100 g / m 2 , more preferably 10 to 50 g / m 2 , and particularly preferably 15 to 30 g / m 2. It is m 2 .
  • the weight per unit of the P3HB-based resin in the coating layer is measured and evaluated by the method described in Examples.
  • the method for manufacturing the laminated body may include the following steps. (A) manufacturing step of water-based coating liquid, (b) feeding step of base material layer, (c) coating step of the water-based coating liquid to the base material layer, (d) drying and film forming step of coating film.
  • step (a) is not particularly limited, but can be performed by the following method. That is, in the step (a), the P3HB-based resin is produced from the microorganism, and the microbial cells containing the P3HB-based resin are crushed in the state of an aqueous dispersion to separate the P3HB-based resin in the cells. Including the process.
  • Control is possible, and treatment can be performed at a low alkali concentration by continuously or intermittently adding alkali, and (iii) a decrease in the molecular weight of the P3HB-based resin can be suppressed, and a high-purity P3HB-based resin can be suppressed. Is separable.
  • the pH of the cell dispersion after addition of alkali is preferably 9 to 13.5. When the pH is 9 or more, the P3HB-based resin tends to be easily separated from the cells, and when the pH is 13.5 or less, the decomposition of the P3HB-based resin tends to be suppressed.
  • the P3HB-based resin can be eluted from the cells by alkaline treatment, the nucleic acid that mainly causes the increase in viscosity can be efficiently crushed, and insoluble substances other than the P3HB-based resin such as cell walls, cell membranes, and insoluble proteins can be sufficiently dispersed.
  • an emulsification disperser for example, a Silberson mixer (manufactured by Silberson), a clear mix (manufactured by MTEC), an Ebara milder (manufactured by Ebara), etc.
  • the temperature conditions for crushing the microbial cells and adding alkali are preferably in the range of room temperature to 50 ° C. If the above temperature condition exceeds 50 ° C., the P3HB-based resin is likely to be decomposed, so that it is preferably around room temperature. In addition, it is not economical because a cooling operation is required to keep the temperature below room temperature.
  • the average particle size of the P3HB-based resin in the aqueous coating liquid is, for example, 0.1 to 50 ⁇ m, preferably 0.5 to 0.5, from the viewpoint of achieving both the productivity of the P3HB-based resin and the uniformity during coating. It is 30 ⁇ m, more preferably 0.8 to 20 ⁇ m.
  • the average particle size is 0.1 ⁇ m or more, the P3HB-based resin can be easily obtained by either the microbial production method or the chemical synthesis method.
  • the average particle size is 50 ⁇ m or less, it is possible to avoid the occurrence of uneven coating.
  • the average particle size of the P3HB-based resin in the aqueous coating liquid is adjusted to a predetermined concentration by using a general-purpose particle size meter such as a Microtrac particle size meter (FRA, manufactured by Nikkiso) and adjusting the aqueous suspension containing the P3HB-based resin to a predetermined concentration.
  • a general-purpose particle size meter such as a Microtrac particle size meter (FRA, manufactured by Nikkiso) and adjusting the aqueous suspension containing the P3HB-based resin to a predetermined concentration.
  • FSA Microtrac particle size meter
  • the aqueous coating liquid does not have to contain an emulsifier, but preferably contains an emulsifier in order to stabilize the coating liquid.
  • the emulsifier include anionic surfactants such as sodium lauryl sulfate and sodium oleate, cationic surfactants such as lauryltrimethylammonium chloride, nonionic surfactants such as glycerin fatty acid ester and sorbitan fatty acid ester, and polyvinyl. Examples thereof include water-soluble polymers such as alcohol and polyvinylpyrrolidone.
  • the amount of the emulsifier added is not particularly limited, but is preferably 1 to 10% by weight based on the solid content of the P3HB resin.
  • the amount of the emulsifier added is 1% by weight or more, the stabilizing effect of the emulsifier tends to be obtained, and when it is 10% by weight or less, the physical properties deteriorate, coloring, etc. due to excessive mixing of the emulsifier into the P3HB resin. It can be avoided.
  • the emulsifier can be added to an aqueous dispersion after crushing and alkaline treatment of microbial cells, centrifugation and washing with water. When washing with methanol, it can be added before or after the solid content concentration of the P3HB resin is adjusted by adding an appropriate amount of water after washing with methanol.
  • steps (b) and (c) are not particularly limited, and can be performed by any method known in the art.
  • the method for manufacturing the laminated body may include (e) a winding step of the laminated body after the step (d).
  • the step (e) is not particularly limited, and may be performed by any method known in the art.
  • the molded body is not particularly limited as long as it includes the laminated body, and is, for example, paper, film, sheet, tube, plate, rod, packaging material (for example, bag), container (for example, bottle container), and parts. And so on.
  • the molded product is preferably a packaging material or a container from the viewpoint of measures against marine pollution.
  • the molded body may be the laminated body itself. Further, in one embodiment of the present invention, the laminated body contained in the molded body may be a secondary processed product.
  • the molded body containing the laminated body can be used as various packaging container materials such as shopping bags, various bag making materials, food / confectionery packaging materials, cups, trays, cartons, etc. (in other words,). , Food, cosmetics, electronics, medicine, medicine, etc.), can be suitably used.
  • the laminate contains a coating layer having high adhesion to a substrate and good heat resistance, the laminate is a container for a liquid, particularly a food and drink cup such as instant noodles, instant soup, and coffee. It can be particularly preferably used as a container for warm contents such as delicatessen, lunch box, tray used for microwave oven food and the like.
  • the heat-sealing temperature at the time of heat-sealing the coating layer of the laminate and the paper as the base material is usually 250 ° C. or lower, preferably 250 ° C. or less when both sides are heated using a heat-not-burn heat-sealing tester having a seal bar. Is 240 ° C. or lower, more preferably 220 ° C. or lower. Within the above range, it is possible to prevent the resin from leaching out in the vicinity of the sealing portion, secure an appropriate film thickness of the coating layer, and secure the sealing strength. Further, the lower limit of the heat seal temperature when a heating type heat seal tester having a seal bar is used is usually 120 ° C. or higher, preferably 140 ° C. or higher.
  • the laminate according to the embodiment of the present invention can exhibit good adhesive strength in a short time after heat sealing even if the heat sealing temperature is high, so that the heat sealing temperature is 170 ° C. or higher. It may be 180 ° C. or higher. According to a particularly preferred embodiment, the heat seal temperature may be 190 ° C. or higher.
  • the heat-sealing pressure when heat-sealing the laminate differs depending on the bonding method.
  • the heat-sealing pressure of the laminate is usually 0.1 MPa or more, preferably 0.3 MPa or more when a heat-not-burn heat-sealing tester having a seal bar is used. Within the above range, appropriate adhesion at the sealed portion can be ensured.
  • another molded body for example, fiber, thread, rope, woven fabric, knitted fabric, non-woven fabric, etc.
  • a material different from the molded body is used. It can also be compounded with paper, film, sheet, tube, board, stick, container, bag, part, foam, etc.). These materials are also preferably biodegradable.
  • An aqueous dispersion containing P3HB3HH having a 3-hydroxyhexanoate unit content of 11 mol% and a weight average molecular weight of 260,000 has a 3-hydroxyhexanoate unit content of 0.7 mol% and a weight average molecular weight of 0.7 mol%.
  • An aqueous dispersion containing 350,000 P3HB3HH was blended with a resin base so as to have a 10% by weight composition.
  • An aqueous coating solution was produced using the blended aqueous dispersion.
  • An aqueous dispersion containing P3HB3HH having a 3-hydroxyhexanoate unit content of 11 mol% and a weight average molecular weight of 260,000 has a 3-hydroxyhexanoate unit content of 0.7 mol% and a weight average molecular weight of 0.7 mol%.
  • An aqueous dispersion containing 350,000 P3HB3HH was blended with a resin base so as to have a 5% by weight composition.
  • An aqueous coating solution was produced using the blended aqueous dispersion.
  • a water-based coating liquid was coated on an A3 size base paper having a basis weight of 200 g / m 2 using a slit coater having a coating thickness of 90 ⁇ m, and then heated in an oven at 160 ° C. for 3 minutes to form a coating layer.
  • the basis weight of the resin content was 20 g / m 2 .
  • the obtained coated paper was subjected to a peeling test.
  • aqueous coating solution was obtained using an aqueous dispersion containing P3HB3HH having a content ratio of 3-hydroxyhexanoate units of 6 mol% and a weight average molecular weight of 250,000.
  • An A3 size base paper having a basis weight of 200 g / m 2 was coated with a water-based coating liquid using a slit coater having a coating thickness of 90 ⁇ m, and then heated in an oven at 160 ° C. for 3 minutes to form a coating layer.
  • the basis weight of the resin content was 20 g / m 2 .
  • the obtained coated paper was subjected to a peeling test.
  • aqueous coating liquids used in Examples 1 to 4 and Comparative Example 1 were coated on a PET film using a slit coater having a coating thickness of 90 ⁇ m, and heated at 160 ° C. for 3 minutes to form a coating layer.
  • the coating layer was peeled off from the PET film and subjected to the following differential scanning calorimetry.
  • 2 to 5 mg of the coating layer is filled in an aluminum pan, and the temperature is raised from 20 ° C. to 190 ° C. at a rate of 10 ° C./min under a nitrogen stream using a differential scanning calorimeter to melt the coating layer and melt the crystals. I got a curve.
  • Table 1 shows the results of the peeling test after 2 seconds of heat sealing of Examples 1 and 2 and Comparative Example 1 when the coating layers were crimped to each other, and the values of Tma, Tmb, and ⁇ Hb / ⁇ Ha.
  • Table 2 shows the results of the peeling test of Examples 1 to 4 and Comparative Example 1 after 2 seconds of heat sealing when the coating layer and the paper were crimped, and the values of Tma, Tmb, and ⁇ Hb / ⁇ Ha.
  • the Tma value and the Tmb value are not significantly different from those of Example 1, but the ⁇ Hb / ⁇ Ha values are 0.25 to 0.51 and 0.12 of Example 1. Showed a greater value than.
  • the paper material was destroyed even when the heat temperature at the time of heat seal was 220 ° C (Table 1) or 190 ° C (Table 2), and even at a higher temperature than in Example 1, immediately after the heat seal. The solidification of the resin proceeded rapidly, and good adhesive strength could be exhibited.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Laminated Bodies (AREA)
PCT/JP2021/033162 2020-09-17 2021-09-09 積層体及び成形体 Ceased WO2022059592A1 (ja)

Priority Applications (4)

Application Number Priority Date Filing Date Title
CN202180063468.3A CN116940467B (zh) 2020-09-17 2021-09-09 层叠体及成型体
EP21869279.6A EP4215366A4 (en) 2020-09-17 2021-09-09 LAMINATE AND MOLDED BODIES
US18/245,596 US12540438B2 (en) 2020-09-17 2021-09-09 Laminated article and molded article
JP2022550510A JP7771070B2 (ja) 2020-09-17 2021-09-09 積層体及び成形体

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JP2020-156003 2020-09-17
JP2020156003 2020-09-17

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023085375A1 (ja) * 2021-11-12 2023-05-19 株式会社カネカ 積層体、およびその利用
JP7285387B1 (ja) 2023-03-07 2023-06-01 日本製紙株式会社 ヒートシール紙
JP2024000453A (ja) * 2022-06-20 2024-01-05 株式会社カネカ 成形体の製造方法、及び成形体
WO2025057612A1 (ja) 2023-09-11 2025-03-20 株式会社カネカ 積層体の製造方法、及び成形体の製造方法
EP4342669A4 (en) * 2021-05-17 2025-04-16 Kaneka Corporation LAMINATE, PACKAGING MATERIAL AND CONTAINER
JP2025517943A (ja) * 2022-06-30 2025-06-12 シージェイ チェイルジェダン コーポレーション 環境にやさしい積層体及びそれを含む包装材

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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