US20050221032A1 - Container of biodegradable heat-resistant hard resin molding - Google Patents

Container of biodegradable heat-resistant hard resin molding Download PDF

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Publication number
US20050221032A1
US20050221032A1 US10/515,387 US51538704A US2005221032A1 US 20050221032 A1 US20050221032 A1 US 20050221032A1 US 51538704 A US51538704 A US 51538704A US 2005221032 A1 US2005221032 A1 US 2005221032A1
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United States
Prior art keywords
layer
shaped container
acid polymer
heat
container
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
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US10/515,387
Inventor
Kazuyuki Yamane
Yukichika Kawakami
Tomoaki Sato
Hisanori Tobita
Takehisa Suzuki
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Kureha Corp
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Kureha Corp
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Assigned to KUREHA CHEMICAL INDUSTRY COMPANY, LIMITED reassignment KUREHA CHEMICAL INDUSTRY COMPANY, LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SATO, TOMOAKI, SUZUKI, TAKEHISA, TOBITA, HISANORI, KAWAKAMI, YUKICHIKA, YAMANE, KAZUYUKI
Publication of US20050221032A1 publication Critical patent/US20050221032A1/en
Assigned to KUREHA CORPORATION reassignment KUREHA CORPORATION CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (AKA KUREHA CHEMICAL INDUSTRY COMPANY, LIMITED)
Abandoned legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B1/00Layered products having a general shape other than plane
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered 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
    • B32B27/08Layered 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/36Layered products comprising a layer of synthetic resin comprising polyesters
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D65/00Wrappers or flexible covers; Packaging materials of special type or form
    • B65D65/38Packaging materials of special type or form
    • B65D65/46Applications of disintegrable, dissolvable or edible materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D65/00Wrappers or flexible covers; Packaging materials of special type or form
    • B65D65/38Packaging materials of special type or form
    • B65D65/46Applications of disintegrable, dissolvable or edible materials
    • B65D65/466Bio- or photodegradable packaging materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/716Degradable
    • B32B2307/7163Biodegradable
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2439/00Containers; Receptacles
    • B32B2439/70Food packaging
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A40/00Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
    • Y02A40/90Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in food processing or handling, e.g. food conservation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W90/00Enabling technologies or technologies with a potential or indirect contribution to greenhouse gas [GHG] emissions mitigation
    • Y02W90/10Bio-packaging, e.g. packing containers made from renewable resources or bio-plastics
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1328Shrinkable or shrunk [e.g., due to heat, solvent, volatile agent, restraint removal, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352Polymer or resin containing [i.e., natural or synthetic]

Definitions

  • the present invention relates to a shaped container of a biodegradable, stiff, heat-resistant and rigid resin, suitable as a temporary preservation container for contents, such as food.
  • Polylactic acid and succinic acid-based aliphatic polyesters, etc. have drawn interest as biodegradable resins harmonizable with environment. If they can be used to form a temporary preservation container for food, the container is expected to be disposed without causing garbage by biodegradation thereof after the use, and also expected be composted together with contents such as food after expiry of the relishable period thereof, thus eliminating an operation, such as separation of materials.
  • these resins are inferior in heat resistance, a container made thereof can be softened or deformed when heated for re-warming the food and can sometimes cause overflow of the contents, thus being liable to cause soiling of the surroundings or scald of the user. Further, a container made of these resins is liable to cause oxidative degradation of the contents such as food, due to gas penetration therethrough.
  • polyglycolic acid is known as a crystalline biodegradable resin having a melting point of 180° C. or higher and a high gas-barrier property, but a relatively thick sheet thereof is liable to cause whitening when shaped under heating, so that the see-through of the resultant shaped container is impaired.
  • a glycolic acid polymer as represented by polyglycolic acid has been proposed to form a gas-barrier composite film by lamination with another thermoplastic resin, such as polylactic acid and succinic acid-based aliphatic polyester (Japanese Laid-Open Application (JP-A) 10-80990), but the use thereof as a material for a shaped container of a rigid resin has not been substantially practiced.
  • a principal object of the present invention is to provide a shaped container of rigid resin which is excellent in biodegradability, stiffness and heat resistance and is suitable as a temporary preservation container of contents, such as food. More specifically, the present invention aims at realizing such a shaped container of rigid resin by a laminate composite shaped container including a glycolic acid polymer as an essential component resin layer.
  • a glycolic acid polymer layer is a resin very suited for providing a shaped container of composite rigid resin as mentioned above excellent in biodegradability, stiffness and heat resistance, if it is disposed together with another biodegradable resin layer in an appropriate positional relationship.
  • a shaped container of biodegradable, heat-resistant and rigid resin having a laminate structure including a glycolic acid polymer layer and another biodegradable resin layer, which has been shaped under heating so that said another biodegradable resin layer forms an outer and/or inner layer.
  • glycolic acid polymer layer is extremely suited for providing a composite shaped container having the above-mentioned properties because it has the following advantageous properties compared with other biodegradable resins, such as lactic acid polymers and succinic acid-based aliphatic polyesters. More specifically, (a) glycolic acid polymer is crystalline and particularly its crystallization speed is remarkably rapid. Moreover, accompanying the crystallization thereof, it provides a resin layer exhibiting a remarkably larger stiffness compared with other biodegradable resins. This property is of course remarkably preferable for providing a rigid resin container.
  • the whitening due to roughening during shaping of the glycolic acid polymer layer surface is caused particularly remarkably on its outer surface subjected to a larger degree of deformation, and accordingly a larger degree of whitening-prevention effect can be attained if another biodegradable resin layer is disposed on an outer surface than an inner surface of the glycolic acid polymer layer.
  • a further better whitening-prevention effect can be attained when such another biodegradable resin layer is disposed on both the outer and inner surfaces of the glycolic acid polymer layer.
  • glycolic acid polymer layer forming the shaped container in lamination with another biodegradable resin layer is crystallized to increase its stiffness during the shaping under heating and optionally performed heat-setting treatment, thereby providing a rigid resin shaped container suitable for temporary preservative storage of food.
  • a lactic acid polymer exhibits a very slow crystallization speed, so that the crystallization thereof hardly proceeds during the heat-setting treatment.
  • glycolic acid polymer is caused to have a remarkably increased heat resistance as high as not to cause a substantial deformability in lamination with another bio-degradable resin layer during 1 minute or longer of heating in a microwave heater.
  • a succinic acid-based polyester has a very low melting point (of ca. 100° C.) and also a low crystallinity, thus being poor in both heat resistance and rigidity (or stiffness).
  • Glycolic acid polymer has a much higher gas-barrier property compared with not only other biodegradable resins as a matter of course but also EVOH (ethylene-vinyl alcohol copolymer) which is a conventionally used representative gas-barrier resin, as high as ca. 3 times or higher (i.e., ca.
  • Glycolic acid polymer has a biodegradability comparable to or even higher than those of other biodegradable resins such as lactic acid polymers and succinic acid-based aliphatic polyester resins. Accordingly, a shaped container having a laminate structure consisting essentially of these biodegradable resin layers can be disposed without causing garbage, by biodegradation thereof after the use as a temporary preservation container for food, etc., and can also be composed together with contents such as food after expiry of the relishable period thereof.
  • the shaped container of biodegradable, heat-resistant and rigid resin according to the present invention has been completed based on the above-mentioned findings.
  • Glycolic acid polymer is a biodegradable (hydrolysable) and crystalline polyester having a recurring unit represented by a formula (1) below: —(OCH 2 CO)— (1)
  • glycolic acid homopolymer consisting only of the above recurring unit, but another recurring unit can be contained provided that a structure having a main chain which can be cut by biodegradation (or hydrolysis) is preferred.
  • Preferable structures may include ester structures including carboxylic acid esters and carbonic acid esters, and amide structure. Particularly, an aliphatic ester structure is preferred in view of biodegradability. Examples thereof may include the following: —(OCHCH 3 CO)— (2) —(OCH 2 CH 2 CH 2 OCO)— (3) —(OCH 2 CH 2 CH 2 CH 2 CO)— (4) The proportion of such another recurring unit structure is below 50 wt. %, preferably below 30 wt. %, further preferably below 15 wt. % in order to retain the effect of increasing stiffness and heat-resistance due to crystallization.
  • thermoplastic resin in the glycolic acid polymer layer for the purpose of controlling the crystallizability thereof in a relatively small amount (e.g., up to 20 wt. %) within an extent of not adversely affecting the stiffness and heat-resistance.
  • thermoplastic resin it is not impossible to use a general-purpose resin, such as polyethylene, polypropylene, polyvinyl chloride or polystyrene, but in order to increase the content of biodegradable resin, it is preferred to use another biodegradable resin, such as a lactic acid polymer, succinic acid-based aliphatic polyester which is a poly-condensate of succinic acid and ethylene diol or butane diol, polycaprolactone, ⁇ -hydroxyacetic acid polycondensate and Biomax (registered trade mark, available from Du Pont), cellulose or starch.
  • a general-purpose resin such as polyethylene, polypropylene, polyvinyl chloride or polystyrene
  • another biodegradable resin such as a lactic acid polymer, succinic acid-based aliphatic polyester which is a poly-condensate of succinic acid and ethylene diol or butane diol, polycaprolactone, ⁇ -hydroxy
  • biodegradable resins such as a lactic acid polymer, succinic acid-based aliphatic polyester which is a poly-condensate of succinic acid and ethylene diol or butane diol, polycaprolactone, ⁇ -hydroxyacetic acid polyconden sate and Biomax (registered trade mark, available from Du Pont), cellulose or starch, raised above as examples of another biodegradable resin which can be incorporated in the glycolic acid polymer layer.
  • biodegradable resins such as a lactic acid polymer, succinic acid-based aliphatic polyester which is a poly-condensate of succinic acid and ethylene diol or butane diol, polycaprolactone, ⁇ -hydroxyacetic acid polyconden sate and Biomax (registered trade mark, available from Du Pont), cellulose or starch, raised above as examples of another biodegradable resin which can be incorporated in the glycolic acid polymer layer.
  • a layer of lactic acid polymer which has a relatively good heat-resistance is preferred to laminate a layer of lactic acid polymer which has a relatively good heat-resistance.
  • a regrind i.e., recovered and re-pulverized product
  • Such a regrind may comprise biodegradable resins, such as glycolic acid polymer, lactic acid polymer and succinic acid-based polyester, can further contain an adhesive resin in some cases, and can be used within an extent of not remarkably lowering the transparency of the shaped container of the present invention.
  • such another biodegradable resin is disposed as at least an outer layer or an inner layer, preferably as an outer layer, with respect to the glycolic acid polymer layer, but may more preferably be disposed as both an outer and an inner layer so as to provide a structure wherein the glycolic acid polymer layer is sandwiched between a pair of other biodegradable resin layers which can be not identical to each other but most preferably each comprise a lactic acid polymer layer.
  • the resultant shaped container may have a layer structure including at least two layers.
  • Examples of such a layer structure may include: another biodegradable resin/glycolic acid polymer/another biodegradable resin (possibly containing a regrind), and another biodegradable resin/regrind/glycolic acid polymer/another biodegradable resin (possibly containing a regrind).
  • the above-mentioned another biodegradable resin layer can have a two-layer structure of different resins, and in this case, the entire layer structure may comprise, for example, succinic acid-based polyester/lactic acid polymer/glycolic acid polymer/lactic acid polymer, which structure may be provided with easy sealability because the succinic acid-based polyester has a relatively low melting point.
  • an adhesive layer can be inserted, as desired, between layers.
  • the shaped container of the present invention is required to have a thickness (a total thickness of the glycolic acid polymer layer and another biodegradable resin layer) of averagely at least 100 ⁇ m, preferably at least 150 mm, particularly preferably 200 ⁇ m or larger.
  • a thickness a total thickness of the glycolic acid polymer layer and another biodegradable resin layer
  • the container is liable to be warped and the handling thereof is liable to be awkward.
  • the upper limit may be determined principally in view of economical factors and generally 5000 ⁇ m or smaller.
  • the glycolic acid polymer layer has a thickness which is 2-98%, more preferably 5-80% of the total thickness of the glycolic acid polymer layer and another bio-degradable resin layer.
  • the shaped container of the present invention can be composed of only the above-mentioned glycolic acid polymer layer and another biodegradable resin layer, and this is preferred in order to increase the biodegradability of the entire container.
  • an adhesive resin layer in order to enhance the inter-layer bonding strength.
  • the adhesive resin epoxy-modified polyolefin, crosslinked ethylene-vinyl acetate copolymer, etc., may preferably be used.
  • the biodegradability of these resins is inferior to the above-mentioned various biodegradable resins, but the load thereof to the environment can be alleviated due to a small amount thereof because the adhesive layer is used in a small thickness of, e.g., ca. 0.5-30 ⁇ m. If an adhesive resin having a better biodegradability is developed, such an adhesive resin may suitably be used in the present invention, of course.
  • the shaped container of the present invention can be directly formed by a melt resin forming method, such as multilayer injection molding, by blow molding (stretch blow molding) of a laminate preform of glycolic acid polymer layer and another biodegradable resin layer formed by such a melt-resin forming method, by direct blow molding, inflation, melt-vacuum forming, or by vacuum forming or deep drawing of a once-formed laminate sheet, as a suitably adoptable technique.
  • the sheet may be pre-heated for 0.5 sec. to 3 min., preferably 1 sec. to 2 min., at 60-120° C., and shaping the sheet so as to fit to a mold by placing the mold under vacuum.
  • the shaping by the melt vacuum forming may be effected by heating at 160-240° C., preferably 170-230° C.
  • the shaped container is provided with increased stiffness and heat-resistance, principally owing to the crystallization of the glycolic acid polymer layer included therein, but can be subjected, as desired, to an additional heat-treatment (heat-setting) for causing further crystallization to increase the stiffness and heat resistance.
  • the heat-treatment is performed at a temperature equal to or higher than a heat-resistant temperature usually required of the shaped container, preferably 100-210° C., more preferably 150-200° C.
  • the heat-treatment time is not particularly restricted but may ordinarily be 1 sec. to 60 min., preferably 2 sec. to 10 min., particularly preferably 5 sec. to 5 min. Heat-treatment for less than 1 sec. may be insufficient in some cases, and a period longer than 60 min. does not provide a substantially different heat-treatment effect but merely results in a longer processing time.
  • the shaped container of the present invention is provided with necessary level of stiffness and heat-resistance.
  • a desirable level of stiffness of the shaped container may be represented by a flexural modulus Ef of at least 100 kg/mm 2 , particularly at least 150 kg/mm 2 as measured in a state where a load is applied from the outer resin layer, and also a factor Ef ⁇ t of at least 1 kg/mm 2 , particularly at least 2 kg/mm, taking the contribution of the thickness t [mm] into consideration.
  • Ef flexural modulus
  • a desired level of heat-resistance of a shaped container of the present invention may be represented by no visible deformation of the container after placing cooked and cooled rice of ca. 180 cm 3 in terms of a dry state volume before the cooking and subjecting the rice in the container to 1 min. of microwave heating at a power of 500 W.
  • the shaped container of the present invention is required to exhibit such a level of whitening resistance as to allow seeing-through of the contents after the shaping under heating. More specifically the shaped container of the present invention is required to exhibit a haze (measured with respect to a cut sheet piece cut out from a side wall of the shaped container according to JIS K6714) of at most 50%, preferably 20. % or below, more preferably 10% or below. If the haze is above 50%, the shaped container is like a frosted glass sheet so that the contents are difficult to judge by seeing-through. In contrast thereto, a haze of 20% or below represents a state of frosted glass sheet not providing a difficulty for determination of the contents, and a haze of 10% or below represents a good see-through of the contents.
  • the thus-obtained rigid resin shaped container of the present invention is extremely suitably used as a temporary preservation container for food which should desirably have heat-resistance, bio-degradability desirable for disposal, stiffness desirable for handling of the container and see-through of the contents, and is also suitably used as a container for medical appliances for which similar properties are desirable, inclusive of heat-resistance for heat-sterilization.
  • the container is shaped into a bottle
  • the bottle is also suitably used as a container for contents, such as a beverage, disliking degradation with oxygen.
  • a regrind of the rigid resin shaped container of the present invention may be utilized, because of its stiffness, for providing chopsticks or tooth picks (though these can be made of young wood lumbered for decreasing the wood population), disposable forks, small blown containers for seasonings, small pouches (which be provided with an easy sealability if laminated with a succinic acid-based polyester), “baran” (i.e., a green sheet provided with a pattern of bamboo leaf), etc., attached to a container for box lunch frequently available in convenience stores, and it becomes possible to compose an entire box lunch set of bio-degradable resins. In this instance, these adjuncts can be poor in transparency.
  • the rigid resin shaped container of the present invention is formed in a shape suitable for accommodating contents, whereas a flat sheet or film having an identical laminate structure can be used as a lid member to be combined with a container of the present invention formed as a bowl or parallelepiped container to form a container accommodating food, etc., capable of microwave heating, by principally utilizing excellent properties, such as gas-barrier property, heat resistance and biodegradability, of the flat sheet or film.
  • such an open bowl or parallel-piped-shaped container of the present invention can also be used in such a manner as to form a temporarily packaged product together with an ordinary food wrapping film, etc., adapted to microwave heating.
  • a container may also be used as a deep-drawn packaging material for storing a stacked sliced ham utilizing its property of heat-resistance, pinhole-resistance or label adhesion, etc., as desired properties. If such a container is required of sealability with a lid material, it is possible to dispose a layer of succinic acid-based polyester outside or inside thereof.
  • the shaped container of the present invention can be combined with a biodegradable film provided separately to provide an entirely biodegradable package.
  • Examples of specific structures thereof may include the following:
  • a shaped container of the present invention together with contents is covered with a bio-degradable film, and the edges of the film are superposed (wrapped) or further sealing the super-posed edges.
  • the sealing may be performed with opposite edges of one inner surface (palm-to-palm sealing) or edges of inner and outer surfaces (envelope sealing or back seaming). (More details of such packaging embodiments are shown in, e.g., JP-A 3-162262 and JP-B 2991526.)
  • the shaped container of the present invention is formed as a container bottom having a flange portion surfaced with a sealable resin, and after contents being placed therein, a lid member comprising a biodegradable film is sealed onto the flange portion of the container bottom to form a package.
  • a lid member comprising a biodegradable film is sealed onto the flange portion of the container bottom to form a package.
  • the package formed in the above-described manner may be passed through a shrink tunnel to shrink the film, thereby providing a beautiful package.
  • the biodegradable (heat-shrinkable) film may have a layer structure of, e.g., lactic acid polymer/glycolic acid polymer/succinic acid-based polyester.
  • An anti-fog agent can be applied on or incorporated in the biodegradable film.
  • Such a biodegradable film may be used instead of a wrapping film (“KUREWRAP”, made by Kureha Chemical Industry Co., Ltd). used in Examples described hereinbelow.
  • the bowl was supported by a jig so as to retain its shape and, in this state, was heat-treated at 120° C. for 1 min. After the heat treatment, the bowl retained its shape even after the jig was removed. The bowl was then placed in an oven at 100° C. but caused no change in outer appearance or shape whereby heat-resistance thereof was confirmed. The bowl exhibited a haze of 10% or below throughout the shaping, heat-treatment and oven-treatment.
  • Cooked and cooled rice was placed in the bowl-shaped product of Example 1, and surface-covered with a wrapping film (“KUREWRAP”, made by Kureha Chemical Industry Co., Ltd.), and in this state, was heated for 1 min. in a microwave heater. After the heating, the bowl caused no change in outer appearance or strength and could be taken out together with the heated rice while holding the bowl by hands, so that its heat resistance could be confirmed.
  • KUREWRAP a wrapping film
  • pellet-form polylactic acid (trade name: “LACTY 9030”, made by Shimadzu Seisakusho) was melted in a heat press at 240° C. by preheating for 1 min. and pressing at 5 MPa for 1 min., and then immediately cooled in iced water to form a 300 ⁇ m-thick single layer sheet. After being dried, the thus-obtained sheet was heated at 240° C. and shaped into a 200 ⁇ m-thick bowl by air-pressure forming. The bowl was supported by a jig so as to retain its shape and, in this state, heat-treated at 120° C. for 1 min. As a result, the bowl was softened at 120° C. and resulted in a shape change after the jig was removed.
  • LACTY 9030 pellet-form polylactic acid
  • a bowl of polylactic acid subjected to heat-treatment in the same manner as in Comparative Example 1 was cooled to room temperature while being supported by the jig, whereby the bowl shape could be retained.
  • Cooked and cooled rice was placed in the bowl after cooling, surface-covered with a wrapping film and then heated for 1 min. in a microwave heater. After the heating, the bowl was deformed, and the heated rice overflowed out of the deformed bowl.
  • Polyglycolic acid (melt viscosity: 2000 Pa ⁇ s at 240° C. and a shear rate of 100/s) was melted in a heat press at 240° C. by preheating for 1 min. and pressing at 5 MPa for 1 min., and then immediately cooled in iced water to form a 250 ⁇ m-thick single-layer sheet. After being dried, the thus-obtained sheet was heated at 240° C. and shaped into a 150 ⁇ m-thick bowl by air-pressure forming. The bowl was supported by a jig so as to retain its shape and, in this state, heat-treated at 120° C. for 1 min. The shaped bowl exhibited a haze of 60%.
  • Polyglycolic acid (PGA), polylactic acid (PLA) (trade name: “LACTY 9030”, made by Shimadzu Seisakusho) and ethylene-glycidyl methacrylate copolymer adhesive resin (“BOND FAST EF-E”, made by Sumitomo Kagaku Kogyo K. K.) were extruded through a 5-layer T-die extruder to form a trans-parent multiplayer sheet having a layer structure of PLA/adhesive resin/PGA/adhesive resin/PLA (having thicknesses from the left of 90/10/100/10/90 ⁇ m).
  • the thus-obtained multilayer sheet was heated at 80° C. for 1 min. and then shaped into a 200 ⁇ m-thick bowl by air-pressure forming. After the shaping, the bowl was supported by a jig so as to retain its shape and, in this state, heat-treated at 150° C. for 1 min.
  • cooked and cooled rice was placed and surface-covered with a wrapping film, followed by heating for 1 min. in a microwave heater. After the heating, the bowl caused no change in outer appearance or strength and could be taken out together with the heated rice with hands, thus confirming its heat resistance.
  • the bowl exhibited a haze of 9% after the microwave heating.
  • the 300 ⁇ m-thick multilayer sheet obtained in Example 3 was shaped under vacuum at 100° C. for 2 sec. by using a continuous deep drawing machine, whereby a sufficiently transparent 160 ⁇ m-thick lunch box-shaped container could be formed. Similar vacuum forming was confirmed to be possible by heating in a range of 80-110° C. for 2 sec. After the shaping, the container was supported by a jig so as to retain a rectangular lunch box shape and heat-treated at 150° C. for 1 min. In the lunch box-shaped rigid container after the heat-treatment, cooked and cooled rice was placed and surface-covered with a wrapping film, followed by heating for 1 min. in a microwave heater. After the heating, the lunch box-shaped rigid container caused no change in outer appearance or strength and could be taken out together with the heated rice with hands, thus confirming its heat resistance. The container exhibited a haze of 9% after the microwave heating.
  • the 300 ⁇ m-thick multilayer sheet obtained in Example 3 was examined with respect to melt-vacuum formability. As a result, it was confirmed possible to prepare a 160 ⁇ m-thick lunch box-shaped container by using an infrared heater set at 200° C. while adjusting the heating time. After the shaping, the container was supported by a jig so as to retain the rectangular lunch box shape and heat-treated at 150° C. for 1 min. In the lunch box-shaped rigid container after the heat-treatment, cooked and cooled rice was placed and surface-covered with a wrapping film, followed by heating for 1 min. in a microwave heater. After the heating, the lunch box-shaped rigid container caused no change in outer appearance or strength and could be taken out together with the heated rice with hands, thus confirming its heat resistance. The container exhibited a haze of 9% after the microwave heating.
  • a rigid resin shaped container which has a laminate structure including a glycolic acid polymer layer and another biodegradable resin layer, is excellent in bio-degradability, stiffness and heat-resistance as well as excellent see-through of contents, and is thus suitable as a temporary preservation container for food, etc.

Abstract

A shaped container of biodegradable, heat-resistant and rigid resin having a laminate structure including a glycolic acid polymer layer and another biodegradable resin layer, is formed by shaping under heating so that another biodegradable resin forms an outer and/or inner layer. The container is excellent in biodegradability, stiffness and heat resistance as well as excellent see-through of contents, and is suitable as a temporary preservation container for food, etc.

Description

    TECHNICAL FIELD
  • The present invention relates to a shaped container of a biodegradable, stiff, heat-resistant and rigid resin, suitable as a temporary preservation container for contents, such as food.
  • BACKGROUND ART
  • Polylactic acid and succinic acid-based aliphatic polyesters, etc., have drawn interest as biodegradable resins harmonizable with environment. If they can be used to form a temporary preservation container for food, the container is expected to be disposed without causing garbage by biodegradation thereof after the use, and also expected be composted together with contents such as food after expiry of the relishable period thereof, thus eliminating an operation, such as separation of materials. However, as these resins are inferior in heat resistance, a container made thereof can be softened or deformed when heated for re-warming the food and can sometimes cause overflow of the contents, thus being liable to cause soiling of the surroundings or scald of the user. Further, a container made of these resins is liable to cause oxidative degradation of the contents such as food, due to gas penetration therethrough.
  • On the other hand, polyglycolic acid is known as a crystalline biodegradable resin having a melting point of 180° C. or higher and a high gas-barrier property, but a relatively thick sheet thereof is liable to cause whitening when shaped under heating, so that the see-through of the resultant shaped container is impaired. Accordingly, though a glycolic acid polymer as represented by polyglycolic acid has been proposed to form a gas-barrier composite film by lamination with another thermoplastic resin, such as polylactic acid and succinic acid-based aliphatic polyester (Japanese Laid-Open Application (JP-A) 10-80990), but the use thereof as a material for a shaped container of a rigid resin has not been substantially practiced.
  • DISCLOSURE OF INVENTION
  • In view of the above-mentioned circumstances, a principal object of the present invention is to provide a shaped container of rigid resin which is excellent in biodegradability, stiffness and heat resistance and is suitable as a temporary preservation container of contents, such as food. More specifically, the present invention aims at realizing such a shaped container of rigid resin by a laminate composite shaped container including a glycolic acid polymer as an essential component resin layer.
  • According to the inventors' study, it has been found that a glycolic acid polymer layer is a resin very suited for providing a shaped container of composite rigid resin as mentioned above excellent in biodegradability, stiffness and heat resistance, if it is disposed together with another biodegradable resin layer in an appropriate positional relationship.
  • More specifically, according to the present invention, there is provided a shaped container of biodegradable, heat-resistant and rigid resin, having a laminate structure including a glycolic acid polymer layer and another biodegradable resin layer, which has been shaped under heating so that said another biodegradable resin layer forms an outer and/or inner layer.
  • The reason why the glycolic acid polymer layer is extremely suited for providing a composite shaped container having the above-mentioned properties is because it has the following advantageous properties compared with other biodegradable resins, such as lactic acid polymers and succinic acid-based aliphatic polyesters. More specifically, (a) glycolic acid polymer is crystalline and particularly its crystallization speed is remarkably rapid. Moreover, accompanying the crystallization thereof, it provides a resin layer exhibiting a remarkably larger stiffness compared with other biodegradable resins. This property is of course remarkably preferable for providing a rigid resin container. (b) However, because of its crystallinity, if a single layer of glycolic acid polymer is shaped under heating for providing a shaped container by, e.g., deep drawing or blow molding, the shaped container is defectively whitened as described above. As a result of the inventors' further study, however, it has been found that the whitening of the single layer of glycolic acid polymer is principally caused as a result of roughening of the surface at which a tension stress is concentrated, and the whitening can be remarkably alleviated if it is laminated with another biodegradable resin layer thereover and then subjected to shaping under heating. The whitening due to roughening during shaping of the glycolic acid polymer layer surface is caused particularly remarkably on its outer surface subjected to a larger degree of deformation, and accordingly a larger degree of whitening-prevention effect can be attained if another biodegradable resin layer is disposed on an outer surface than an inner surface of the glycolic acid polymer layer. However, a further better whitening-prevention effect can be attained when such another biodegradable resin layer is disposed on both the outer and inner surfaces of the glycolic acid polymer layer. (c) The glycolic acid polymer layer forming the shaped container in lamination with another biodegradable resin layer is crystallized to increase its stiffness during the shaping under heating and optionally performed heat-setting treatment, thereby providing a rigid resin shaped container suitable for temporary preservative storage of food. (In contrast thereto, a lactic acid polymer exhibits a very slow crystallization speed, so that the crystallization thereof hardly proceeds during the heat-setting treatment.) (d) Further, glycolic acid polymer is caused to have a remarkably increased heat resistance as high as not to cause a substantial deformability in lamination with another bio-degradable resin layer during 1 minute or longer of heating in a microwave heater. (Incidentally, a succinic acid-based polyester has a very low melting point (of ca. 100° C.) and also a low crystallinity, thus being poor in both heat resistance and rigidity (or stiffness). (e) Glycolic acid polymer has a much higher gas-barrier property compared with not only other biodegradable resins as a matter of course but also EVOH (ethylene-vinyl alcohol copolymer) which is a conventionally used representative gas-barrier resin, as high as ca. 3 times or higher (i.e., ca. ⅓ or lower in terms of an oxygen transmission co-efficient) as that of EVOH, so that it can provide, e.g., a bottle shaped therefrom, exhibiting a remarkably enhanced effect of preserving the contents in the bottle. (f) Glycolic acid polymer has a biodegradability comparable to or even higher than those of other biodegradable resins such as lactic acid polymers and succinic acid-based aliphatic polyester resins. Accordingly, a shaped container having a laminate structure consisting essentially of these biodegradable resin layers can be disposed without causing garbage, by biodegradation thereof after the use as a temporary preservation container for food, etc., and can also be composed together with contents such as food after expiry of the relishable period thereof.
  • The shaped container of biodegradable, heat-resistant and rigid resin according to the present invention has been completed based on the above-mentioned findings.
  • EMBODIMENTS OF THE INVENTION
  • (Glycolic Acid Polymer)
  • Glycolic acid polymer is a biodegradable (hydrolysable) and crystalline polyester having a recurring unit represented by a formula (1) below:
    —(OCH2CO)—  (1)
  • It is preferred to use glycolic acid homopolymer (PGA) consisting only of the above recurring unit, but another recurring unit can be contained provided that a structure having a main chain which can be cut by biodegradation (or hydrolysis) is preferred.
  • Preferable structures may include ester structures including carboxylic acid esters and carbonic acid esters, and amide structure. Particularly, an aliphatic ester structure is preferred in view of biodegradability. Examples thereof may include the following:
    —(OCHCH3CO)—  (2)
    —(OCH2CH2CH2OCO)—  (3)
    —(OCH2CH2CH2CH2CO)—  (4)
    The proportion of such another recurring unit structure is below 50 wt. %, preferably below 30 wt. %, further preferably below 15 wt. % in order to retain the effect of increasing stiffness and heat-resistance due to crystallization.
  • Further, it is also possible to incorporate another thermoplastic resin in the glycolic acid polymer layer for the purpose of controlling the crystallizability thereof in a relatively small amount (e.g., up to 20 wt. %) within an extent of not adversely affecting the stiffness and heat-resistance.
  • As for such another thermoplastic resin, it is not impossible to use a general-purpose resin, such as polyethylene, polypropylene, polyvinyl chloride or polystyrene, but in order to increase the content of biodegradable resin, it is preferred to use another biodegradable resin, such as a lactic acid polymer, succinic acid-based aliphatic polyester which is a poly-condensate of succinic acid and ethylene diol or butane diol, polycaprolactone, ω-hydroxyacetic acid polycondensate and Biomax (registered trade mark, available from Du Pont), cellulose or starch.
  • (Another Biodegradable Resin)
  • As for a constituent resin of said another biodegradable resin for forming the rigid resin shaped container of the present invention together with the glycolic acid polymer layer it is possible to use biodegradable resins, such as a lactic acid polymer, succinic acid-based aliphatic polyester which is a poly-condensate of succinic acid and ethylene diol or butane diol, polycaprolactone, ω-hydroxyacetic acid polyconden sate and Biomax (registered trade mark, available from Du Pont), cellulose or starch, raised above as examples of another biodegradable resin which can be incorporated in the glycolic acid polymer layer. Among these, it is preferred to laminate a layer of lactic acid polymer which has a relatively good heat-resistance. As an example of such another biodegradable resin, it is also possible to use a regrind (i.e., recovered and re-pulverized product) of a rigid resin shaped container of the present invention. Such a regrind may comprise biodegradable resins, such as glycolic acid polymer, lactic acid polymer and succinic acid-based polyester, can further contain an adhesive resin in some cases, and can be used within an extent of not remarkably lowering the transparency of the shaped container of the present invention.
  • In the shaped container of the present invention, such another biodegradable resin is disposed as at least an outer layer or an inner layer, preferably as an outer layer, with respect to the glycolic acid polymer layer, but may more preferably be disposed as both an outer and an inner layer so as to provide a structure wherein the glycolic acid polymer layer is sandwiched between a pair of other biodegradable resin layers which can be not identical to each other but most preferably each comprise a lactic acid polymer layer. The resultant shaped container may have a layer structure including at least two layers. Examples of such a layer structure may include: another biodegradable resin/glycolic acid polymer/another biodegradable resin (possibly containing a regrind), and another biodegradable resin/regrind/glycolic acid polymer/another biodegradable resin (possibly containing a regrind). The above-mentioned another biodegradable resin layer can have a two-layer structure of different resins, and in this case, the entire layer structure may comprise, for example, succinic acid-based polyester/lactic acid polymer/glycolic acid polymer/lactic acid polymer, which structure may be provided with easy sealability because the succinic acid-based polyester has a relatively low melting point. In any case, an adhesive layer can be inserted, as desired, between layers.
  • (Thickness)
  • In order to be a rigid resin shaped container having a good stiffness after an appropriate degree of heat treatment, the shaped container of the present invention is required to have a thickness (a total thickness of the glycolic acid polymer layer and another biodegradable resin layer) of averagely at least 100 μm, preferably at least 150 mm, particularly preferably 200 μm or larger. Below 100 μm, when the container is caused to receive a relatively heavy food, such as fried food, daily dishes or cooked rice, the container is liable to be warped and the handling thereof is liable to be awkward. The upper limit may be determined principally in view of economical factors and generally 5000 μm or smaller.
  • Further, in order to ensure a necessary stiffness while retaining the whitening prevention effect owing to the lamination, it is preferred the glycolic acid polymer layer has a thickness which is 2-98%, more preferably 5-80% of the total thickness of the glycolic acid polymer layer and another bio-degradable resin layer.
  • (Adhesive Layer)
  • The shaped container of the present invention can be composed of only the above-mentioned glycolic acid polymer layer and another biodegradable resin layer, and this is preferred in order to increase the biodegradability of the entire container. In the case of once forming a multilayer sheet and then shaping the sheet by secondary processing, such as (deep) drawing or blow forming, etc., however, it is possible to insert an adhesive resin layer in order to enhance the inter-layer bonding strength. As the adhesive resin, epoxy-modified polyolefin, crosslinked ethylene-vinyl acetate copolymer, etc., may preferably be used. The biodegradability of these resins is inferior to the above-mentioned various biodegradable resins, but the load thereof to the environment can be alleviated due to a small amount thereof because the adhesive layer is used in a small thickness of, e.g., ca. 0.5-30 μm. If an adhesive resin having a better biodegradability is developed, such an adhesive resin may suitably be used in the present invention, of course.
  • (Shaping Under Heating)
  • The shaped container of the present invention can be directly formed by a melt resin forming method, such as multilayer injection molding, by blow molding (stretch blow molding) of a laminate preform of glycolic acid polymer layer and another biodegradable resin layer formed by such a melt-resin forming method, by direct blow molding, inflation, melt-vacuum forming, or by vacuum forming or deep drawing of a once-formed laminate sheet, as a suitably adoptable technique. According to the vacuum forming, the sheet may be pre-heated for 0.5 sec. to 3 min., preferably 1 sec. to 2 min., at 60-120° C., and shaping the sheet so as to fit to a mold by placing the mold under vacuum. The shaping by the melt vacuum forming may be effected by heating at 160-240° C., preferably 170-230° C.
  • (Heat Treatment)
  • Through the above-mentioned shaping under heating, the shaped container is provided with increased stiffness and heat-resistance, principally owing to the crystallization of the glycolic acid polymer layer included therein, but can be subjected, as desired, to an additional heat-treatment (heat-setting) for causing further crystallization to increase the stiffness and heat resistance. The heat-treatment is performed at a temperature equal to or higher than a heat-resistant temperature usually required of the shaped container, preferably 100-210° C., more preferably 150-200° C.
  • The heat-treatment time is not particularly restricted but may ordinarily be 1 sec. to 60 min., preferably 2 sec. to 10 min., particularly preferably 5 sec. to 5 min. Heat-treatment for less than 1 sec. may be insufficient in some cases, and a period longer than 60 min. does not provide a substantially different heat-treatment effect but merely results in a longer processing time.
  • (Stiffness, Heat Resistance)
  • Through the above-mentioned shaping under heating and optional heat-treatment, the shaped container of the present invention is provided with necessary level of stiffness and heat-resistance.
  • A desirable level of stiffness of the shaped container may be represented by a flexural modulus Ef of at least 100 kg/mm2, particularly at least 150 kg/mm2 as measured in a state where a load is applied from the outer resin layer, and also a factor Ef×t of at least 1 kg/mm2, particularly at least 2 kg/mm, taking the contribution of the thickness t [mm] into consideration. These values can be also measured, e.g., in the case of sheet forming (shaping), by subjecting a sheet before the shaping to a quantity of heat provided to the sheet during the actual shaping under heating and heat-treatment, then subjecting the heated sheet to the flexure test and applying a correction to the measured values corresponding to a thickness reduction after the shaping.
  • A desired level of heat-resistance of a shaped container of the present invention may be represented by no visible deformation of the container after placing cooked and cooled rice of ca. 180 cm3 in terms of a dry state volume before the cooking and subjecting the rice in the container to 1 min. of microwave heating at a power of 500 W.
  • (Whitening)
  • The shaped container of the present invention is required to exhibit such a level of whitening resistance as to allow seeing-through of the contents after the shaping under heating. More specifically the shaped container of the present invention is required to exhibit a haze (measured with respect to a cut sheet piece cut out from a side wall of the shaped container according to JIS K6714) of at most 50%, preferably 20. % or below, more preferably 10% or below. If the haze is above 50%, the shaped container is like a frosted glass sheet so that the contents are difficult to judge by seeing-through. In contrast thereto, a haze of 20% or below represents a state of frosted glass sheet not providing a difficulty for determination of the contents, and a haze of 10% or below represents a good see-through of the contents.
  • (Use)
  • The thus-obtained rigid resin shaped container of the present invention is extremely suitably used as a temporary preservation container for food which should desirably have heat-resistance, bio-degradability desirable for disposal, stiffness desirable for handling of the container and see-through of the contents, and is also suitably used as a container for medical appliances for which similar properties are desirable, inclusive of heat-resistance for heat-sterilization. Further, in case where the container is shaped into a bottle, the bottle is also suitably used as a container for contents, such as a beverage, disliking degradation with oxygen. Further, a regrind of the rigid resin shaped container of the present invention may be utilized, because of its stiffness, for providing chopsticks or tooth picks (though these can be made of young wood lumbered for decreasing the wood population), disposable forks, small blown containers for seasonings, small pouches (which be provided with an easy sealability if laminated with a succinic acid-based polyester), “baran” (i.e., a green sheet provided with a pattern of bamboo leaf), etc., attached to a container for box lunch frequently available in convenience stores, and it becomes possible to compose an entire box lunch set of bio-degradable resins. In this instance, these adjuncts can be poor in transparency.
  • Incidentally, the rigid resin shaped container of the present invention is formed in a shape suitable for accommodating contents, whereas a flat sheet or film having an identical laminate structure can be used as a lid member to be combined with a container of the present invention formed as a bowl or parallelepiped container to form a container accommodating food, etc., capable of microwave heating, by principally utilizing excellent properties, such as gas-barrier property, heat resistance and biodegradability, of the flat sheet or film.
  • However, such an open bowl or parallel-piped-shaped container of the present invention can also be used in such a manner as to form a temporarily packaged product together with an ordinary food wrapping film, etc., adapted to microwave heating. Further, such a container may also be used as a deep-drawn packaging material for storing a stacked sliced ham utilizing its property of heat-resistance, pinhole-resistance or label adhesion, etc., as desired properties. If such a container is required of sealability with a lid material, it is possible to dispose a layer of succinic acid-based polyester outside or inside thereof.
  • The shaped container of the present invention can be combined with a biodegradable film provided separately to provide an entirely biodegradable package. Examples of specific structures thereof may include the following:
  • 1) A shaped container of the present invention together with contents is covered with a bio-degradable film, and the edges of the film are superposed (wrapped) or further sealing the super-posed edges. The sealing may be performed with opposite edges of one inner surface (palm-to-palm sealing) or edges of inner and outer surfaces (envelope sealing or back seaming). (More details of such packaging embodiments are shown in, e.g., JP-A 3-162262 and JP-B 2991526.)
  • 2) The shaped container of the present invention is formed as a container bottom having a flange portion surfaced with a sealable resin, and after contents being placed therein, a lid member comprising a biodegradable film is sealed onto the flange portion of the container bottom to form a package. (Details of this embodiment are shown in, e.g., JP-A 4-72135.)
  • In either of the above-mentioned embodiments 1) and 2), if the biodegradable film is heat-shrinkable, the package formed in the above-described manner may be passed through a shrink tunnel to shrink the film, thereby providing a beautiful package.
  • The biodegradable (heat-shrinkable) film may have a layer structure of, e.g., lactic acid polymer/glycolic acid polymer/succinic acid-based polyester. An anti-fog agent can be applied on or incorporated in the biodegradable film. Such a biodegradable film may be used instead of a wrapping film (“KUREWRAP”, made by Kureha Chemical Industry Co., Ltd). used in Examples described hereinbelow.
  • EXAMPLES
  • Hereinbelow, the present invention will be described more specifically based on Examples and Comparative Examples.
  • Example 1
  • 2 g of pellet form polylactic acid (“LACTY”, made by Shimadzu Seisakusho K.K.) were placed on a 15 cm-dia. and 200 μm-thick amorphous sheet of poly-glycolic acid (exhibiting a melt viscosity of 2000 Pa·s at 240° C. and a shear rate of 100/s), and melted in a heat press at 240° C. by preheating for 1 min. and pressing at 5 MPa for 1 min., followed immediately by cooling in iced water to form a 300 μm-thick transparent laminate sheet. After being dried, the thus-obtained sheet was shaped into a 200 μm-thick bowl with an outer layer of the polylactic acid by air-pressure forming. The bowl was supported by a jig so as to retain its shape and, in this state, was heat-treated at 120° C. for 1 min. After the heat treatment, the bowl retained its shape even after the jig was removed. The bowl was then placed in an oven at 100° C. but caused no change in outer appearance or shape whereby heat-resistance thereof was confirmed. The bowl exhibited a haze of 10% or below throughout the shaping, heat-treatment and oven-treatment.
  • Example 2
  • Cooked and cooled rice was placed in the bowl-shaped product of Example 1, and surface-covered with a wrapping film (“KUREWRAP”, made by Kureha Chemical Industry Co., Ltd.), and in this state, was heated for 1 min. in a microwave heater. After the heating, the bowl caused no change in outer appearance or strength and could be taken out together with the heated rice while holding the bowl by hands, so that its heat resistance could be confirmed.
  • Comparative Example 1
  • 7 g of pellet-form polylactic acid (trade name: “LACTY 9030”, made by Shimadzu Seisakusho) was melted in a heat press at 240° C. by preheating for 1 min. and pressing at 5 MPa for 1 min., and then immediately cooled in iced water to form a 300 μm-thick single layer sheet. After being dried, the thus-obtained sheet was heated at 240° C. and shaped into a 200 μm-thick bowl by air-pressure forming. The bowl was supported by a jig so as to retain its shape and, in this state, heat-treated at 120° C. for 1 min. As a result, the bowl was softened at 120° C. and resulted in a shape change after the jig was removed.
  • Comparative Example 2
  • A bowl of polylactic acid subjected to heat-treatment in the same manner as in Comparative Example 1 was cooled to room temperature while being supported by the jig, whereby the bowl shape could be retained. Cooked and cooled rice was placed in the bowl after cooling, surface-covered with a wrapping film and then heated for 1 min. in a microwave heater. After the heating, the bowl was deformed, and the heated rice overflowed out of the deformed bowl.
  • Comparative Example 3
  • Polyglycolic acid (melt viscosity: 2000 Pa·s at 240° C. and a shear rate of 100/s) was melted in a heat press at 240° C. by preheating for 1 min. and pressing at 5 MPa for 1 min., and then immediately cooled in iced water to form a 250 μm-thick single-layer sheet. After being dried, the thus-obtained sheet was heated at 240° C. and shaped into a 150 μm-thick bowl by air-pressure forming. The bowl was supported by a jig so as to retain its shape and, in this state, heat-treated at 120° C. for 1 min. The shaped bowl exhibited a haze of 60%.
  • Example 3
  • Polyglycolic acid (PGA), polylactic acid (PLA) (trade name: “LACTY 9030”, made by Shimadzu Seisakusho) and ethylene-glycidyl methacrylate copolymer adhesive resin (“BOND FAST EF-E”, made by Sumitomo Kagaku Kogyo K. K.) were extruded through a 5-layer T-die extruder to form a trans-parent multiplayer sheet having a layer structure of PLA/adhesive resin/PGA/adhesive resin/PLA (having thicknesses from the left of 90/10/100/10/90 μm).
  • The thus-obtained multilayer sheet was heated at 80° C. for 1 min. and then shaped into a 200 μm-thick bowl by air-pressure forming. After the shaping, the bowl was supported by a jig so as to retain its shape and, in this state, heat-treated at 150° C. for 1 min. In the bowl-shaped rigid container, cooked and cooled rice was placed and surface-covered with a wrapping film, followed by heating for 1 min. in a microwave heater. After the heating, the bowl caused no change in outer appearance or strength and could be taken out together with the heated rice with hands, thus confirming its heat resistance. The bowl exhibited a haze of 9% after the microwave heating.
  • Example 4
  • The 300 μm-thick multilayer sheet obtained in Example 3 was shaped under vacuum at 100° C. for 2 sec. by using a continuous deep drawing machine, whereby a sufficiently transparent 160 μm-thick lunch box-shaped container could be formed. Similar vacuum forming was confirmed to be possible by heating in a range of 80-110° C. for 2 sec. After the shaping, the container was supported by a jig so as to retain a rectangular lunch box shape and heat-treated at 150° C. for 1 min. In the lunch box-shaped rigid container after the heat-treatment, cooked and cooled rice was placed and surface-covered with a wrapping film, followed by heating for 1 min. in a microwave heater. After the heating, the lunch box-shaped rigid container caused no change in outer appearance or strength and could be taken out together with the heated rice with hands, thus confirming its heat resistance. The container exhibited a haze of 9% after the microwave heating.
  • Example 5
  • The 300 μm-thick multilayer sheet obtained in Example 3 was examined with respect to melt-vacuum formability. As a result, it was confirmed possible to prepare a 160 μm-thick lunch box-shaped container by using an infrared heater set at 200° C. while adjusting the heating time. After the shaping, the container was supported by a jig so as to retain the rectangular lunch box shape and heat-treated at 150° C. for 1 min. In the lunch box-shaped rigid container after the heat-treatment, cooked and cooled rice was placed and surface-covered with a wrapping film, followed by heating for 1 min. in a microwave heater. After the heating, the lunch box-shaped rigid container caused no change in outer appearance or strength and could be taken out together with the heated rice with hands, thus confirming its heat resistance. The container exhibited a haze of 9% after the microwave heating.
  • INDUSTRIAL APPLICABILITY
  • As described above, according to the present invention, there is provided a rigid resin shaped container, which has a laminate structure including a glycolic acid polymer layer and another biodegradable resin layer, is excellent in bio-degradability, stiffness and heat-resistance as well as excellent see-through of contents, and is thus suitable as a temporary preservation container for food, etc.

Claims (14)

1. A shaped container of biodegradable, heat-resistant and rigid resin, having a laminate structure including a glycolic acid polymer layer and another biodegradable resin layer, which has been shaped under heating so that said another biodegradable resin layer forms an outer and/or inner layer.
2. A shaped container according to claim 1, wherein said another biodegradable resin layer is disposed at least as the outer layer outside the glycolic acid polymer layer.
3. A shaped container according to claim 2, wherein said outer layer of another biodegradable resin comprises a lactic acid polymer.
4. A shaped container according to claim 2, further including said another biodegradable resin layer also as an inner layer disposed inside the glycolic acid polymer layer.
5. A shaped container according to claim 4, wherein said inner layer of another biodegradable resin comprises a lactic acid polymer.
6. A shaped container according to 5 claim 1, further including an adhesive layer between the glycolic acid polymer layer and the outer and/or inner biodegradable resin layer.
7. A shaped container according to claim 1, wherein the glycolic acid polymer layer and another biodegradable resin layer have a total thickness of 100-5000 μm, of which the thickness of the glycolic acid polymer layer occupies 2-98%.
8. A shaped container according to claim 1, which has been treated for heat-setting after the shaping under heating.
9. A shaped container according to claim 1, exhibiting a flexural modulus Ef of at least 100 kg/mm2 as measured in a state where a load is applied from the outer resin layer.
10. A shaped container according to claim 9, exhibiting a flexural modulus Ef (as measured in a state where a load is applied to the outer resin layer) and a container thickness t giving a product Ef×t of at least 1 kg/mm.
11. A package, comprising a shaped container of biodegradable, heat-resistant and rigid resin according to claim 1 and a biodegradable film.
12. A package according to claim 11, wherein the biodegradable film is heat-shrinkable.
13. A package according to claim 11 wherein the biodegradable film includes at least one glycolic acid polymer layer.
14. A package according to claim 12, wherein the biodegradable film has a gas-barrier property.
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US20070255013A1 (en) * 2006-04-27 2007-11-01 Becraft Michael L Polymeric blend comprising polylactic acid
US20070254118A1 (en) * 2006-04-27 2007-11-01 Slawomir Opusko Multilayer film comprising polylactic acid
US20080050603A1 (en) * 2004-06-23 2008-02-28 Randall Jed R Branched Polylactic Acid Polymer and Method of Preparing Same
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US20080193787A1 (en) * 2005-03-25 2008-08-14 Resilux Preform For Blowmolding Thereof Into a Container and Process For Manufacturing Thereof
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WO2003099558A1 (en) 2003-12-04
EP1550549A1 (en) 2005-07-06
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AU2003235451B2 (en) 2010-01-21
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ATE521471T1 (en) 2011-09-15
AU2003235451A1 (en) 2003-12-12
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EP1550549B1 (en) 2011-08-24
JPWO2003099558A1 (en) 2005-09-22

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