WO2001048064A1 - Procede de sechage et de stockage de resine desoxygenante ou de matiere de conditionnement desoxygenante - Google Patents

Procede de sechage et de stockage de resine desoxygenante ou de matiere de conditionnement desoxygenante Download PDF

Info

Publication number
WO2001048064A1
WO2001048064A1 PCT/JP1999/007316 JP9907316W WO0148064A1 WO 2001048064 A1 WO2001048064 A1 WO 2001048064A1 JP 9907316 W JP9907316 W JP 9907316W WO 0148064 A1 WO0148064 A1 WO 0148064A1
Authority
WO
WIPO (PCT)
Prior art keywords
oxygen
absorbing
packaging material
resin
container
Prior art date
Application number
PCT/JP1999/007316
Other languages
English (en)
Japanese (ja)
Inventor
Yuki Miyazawa
Yoshihiro Kobayashi
Toru Ikeda
Shigenobu Harano
Masao Yamane
Original Assignee
Ajinomoto Co., Inc.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ajinomoto Co., Inc. filed Critical Ajinomoto Co., Inc.
Priority to PCT/JP1999/007316 priority Critical patent/WO2001048064A1/fr
Publication of WO2001048064A1 publication Critical patent/WO2001048064A1/fr

Links

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
    • 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
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/22Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
    • B01J20/26Synthetic macromolecular compounds

Definitions

  • the present invention relates to a method for drying and preserving an oxygen-absorbing resin or an oxygen-absorbing packaging material.
  • the composition of the oxygen absorbent is disclosed in Japanese Patent Publication No. 53-141185, which discloses a combination of reduced iron (main agent) and an oxidation promoter such as calcium chloride.
  • an oxidation promoter such as calcium chloride.
  • some calcium chlorides have water of crystallization, and the existence of hexahydrate, tetrahydrate, dihydrate and monohydrate is known. It has been confirmed from the absorption curve of the differential thermal analysis that the water of crystallization is desorbed by heating and becomes an anhydrous salt (anhydrous) at 200 ° C. according to the present inventors.
  • Calcium chloride is also used as a desiccant, and it is known that not only anhydrous salts but also dihydrates have hygroscopicity.
  • the oxygen-absorbing performance of the resin containing oxygen scavenger was improved by mixing and dispersing calcium chloride as an oxidation promoter in addition to the reduced iron as the main agent as the oxygen scavenger.
  • a resin containing an oxygen-absorbing agent in which it is blended and dispersed, a packaging material containing an oxygen-absorbing agent, and a packaging material containing the oxygen-absorbing agent prepared using the resin are processed.
  • the containers containing oxygen absorbers prepared in this way have improved their own hygroscopicity and, consequently, improved their oxygen absorbing function, they have problems with hygroscopicity during storage of them and the secondary problems associated with them. This has led to the problem of preventing moisture absorption.
  • the storage period is also the same.
  • the deoxygenation ability was reduced during storage, and foaming occurred when the stored packaging material was thermoformed into a container or when the content of the stored container was filled and heat sealed.
  • a so-called self-reactive reaction method in which the minimum amount of water necessary for the start of deoxygenation is retained in a storage bag so that it works even in low-moisture environments.
  • a resin containing an oxygen scavenger which is stored by removing oxygen in the head space, enclosed with the oxygen scavenger sachet, made using this resin It is conceivable to maintain the oxygen-absorbing ability (oxygen absorption performance) of the oxygen-absorbing agent-containing packaging material and the oxygen-absorbing agent-containing container made using this packaging material.
  • the oxygen scavenger sachet is enclosed, the oxygen in the head space is completely removed and the oxygen scavenging ability can be maintained, but on the other hand, the water contained in the oxygen scavenger sachet deoxygenates It migrates to resin-containing resin, etc., which causes foaming during thermoforming after storage.
  • packaging materials with deoxygenation performance reaching the practical range have been developed, no storage method suitable for maintaining their performance and performing stable thermoforming has been found at present. It is.
  • the present invention relates to a deoxidizing resin containing a deoxidizing agent, a deoxidizing packaging material formed by laminating the deoxidizing resin with another material, and a deoxidizing container prepared by processing the packaging material.
  • the purpose of the present invention is to provide a dry preservation method which is effective in preventing defoaming capacity (oxygen absorption capacity) from lowering and preventing foaming during the preparation of packaging materials, heat processing molding of containers, or heat sealing.
  • the present inventors have conducted intensive studies to achieve this object, and as a result, have removed by heating the water of crystallization and other water contained in the metal halide salt used as the oxidation promoter in the oxygen scavenger.
  • the present inventors have found that storage in a dry state can prevent the oxygen-absorbing resin and the oxygen-absorbing wrapping material from deteriorating in oxygen-absorbing ability and prevent foaming during thermal processing and the like, and thus completed the present invention.
  • the present invention provides a deoxidizing resin containing a deoxidizing agent composed of at least iron powder and a metal halide, and a deoxidizing packaging material formed by laminating the deoxidizing resin with another material.
  • This packaging material also includes a laminate of an intermediate product that should be completed by laminating with other (laminated) materials.
  • a deoxidizing container made by processing this deoxidizing packaging material The water of crystallization of the metal halide salt is removed and is substantially anhydrous.
  • the present invention relates to a method for drying and preserving an oxygen-absorbing resin or an oxygen-absorbing packaging material, characterized in that the oxygen-absorbing resin or the oxygen-absorbing packaging material is sealed and stored in a water vapor barrier packaging container together with a desiccant.
  • the oxygen scavenger used in the present invention is composed of at least iron powder (main agent) and a metal halide salt.
  • iron powder a fine particle having an average particle diameter of 7 to 20 / i and an apparent density of 2.3 g / cm 3 or more is preferably used, although the particle diameter is not particularly limited.
  • iron powder include iron powder such as reduced iron powder and sprayed iron powder, as well as iron powder obtained by crushing iron, steel chips, ground iron chips and the like.
  • metal halide examples include alkaline earth metal halides and alkali metal halides.
  • alkali metal halides such as calcium chloride and magnesium chloride are exemplified. These may be used alone, but may be used as a mixture with each other or with a halogenated alkali metal salt such as sodium chloride.
  • the oxygen scavenger is prepared by milling the fine metal powder (main agent) and the metal halide (oxidation accelerator) under an inert atmosphere such as nitrogen using a dry milling method. It is preferable to coat the iron powder while the powder is being coated, or in some cases, to coat the surface of the iron powder with a metal halide salt while grinding both.
  • the mixing ratio of these two is appropriately adjusted depending on the intended use such as the required oxygen absorption rate, but the oxidation promoter can be, for example, 1 to 40 parts by weight per 1 part by weight of the main agent.
  • the water content of the oxygen absorbent prepared in this manner is preferably not more than 8,000 ppm from the viewpoint of ensuring dehydration in the next dehydration step, and more preferably not more than 3,000 ppm. Particularly preferred is 0 ppm or less.
  • the preparation of the oxygen-absorbing resin containing the oxygen-absorbing agent that can be prepared in this manner.
  • a polyolefin resin heated and melted using a vented twin-screw extruder or the like is used. After dispersing the oxygen scavenger, it is pelletized to obtain a resin having deoxidizing ability, that is, an oxygen scavenging resin.
  • the mixing ratio of the oxygen scavenger and the polyolefin resin may be any of the compound composition, the masterbatch composition, etc., but the oxygen scavenger is, for example, 0.01 to 0.5 parts by weight per 1 part by weight of the resin. Can be.
  • the present invention will be described by taking, as an example, the case where calcium chloride is used as the metal halide salt (oxidation accelerator) of the oxygen scavenger.
  • calcium chloride concentrates as an aqueous solution, it becomes hexahydrate at about 30 ° C or lower, tetrahydrate at about 30-40 ° C, and dihydrate at about 30-40 ° C. Precipitates.
  • dihydrate is further said to be monohydrate at 175 ° C and anhydrous at about 3 ° C, and is said to be Dictionary)), or it is said that it becomes anhydrous at 200 ° C (Iwanami Shoten Publishing Co., Ltd., published in 1998). In the same way as in the latter dictionary, heating at about 200 ° C or more turns it into an anhydride.
  • the dry storage method of the present invention can be advantageously applied to a deoxidized resin prepared by heating and kneading at 200 ° C. or more.
  • the temperature higher than the crystallization water desorption temperature at which the water of crystallization deviates and shifts to an anhydrous salt by more than 20 ° C is 220 ° C.
  • this is an equilibrium temperature, so it takes time to desorb crystallization water and complete desorption is difficult. It is heating.
  • the upper limit of the heating temperature is a temperature at which the quality of the matrix resin does not deteriorate due to heating.
  • the oxygen absorbing agent of the oxygen scavenger according to the present invention has a sufficient hygroscopic power as long as it has the hygroscopic power of calcium chloride anhydride.
  • a desiccant having substantially the same or higher hygroscopicity as a metal halide anhydride to be sealed in a water vapor barrier-compatible packaging container together with an oxygen-absorbing resin to be dried and stored (Hereinafter, it may be simply referred to as "the desiccant”.)
  • hygroscopicity excess adsorption
  • a substantially equivalent or higher hygroscopicity means that it is substantially equivalent to an anhydrous calcium chloride or magnesium chloride indicated within the range of storage conditions (temperature and humidity) of the deoxidizing resin by an isothermal adsorption (hygroscopic) line.
  • hygroscopic isothermal adsorption
  • Examples of such a desiccant include calcium chloride, magnesium chloride, silica gel, zeolite, synthetic zeolite, activated clay, and the like, which have the above-mentioned hygroscopicity.
  • the above-described free water and adsorbed water are removed by enclosing the oxygen-absorbing resin and the present desiccant in a steam-barrier package and hermetically sealing the package.
  • the dry preservation method of the present invention in this manner, the free water existing in the deoxidizing resin and the free water The adsorbed water on the surface of the resin pellets is removed, preventing a decrease in the deoxidizing capacity during storage.
  • the deoxidizing resin is heated and melted, and this is laminated with other materials to deoxygenate packaging. This makes it possible to prevent foaming during processing into materials, which in turn facilitates the production of such deoxidized packaging materials.
  • the drying and preservation method of the present invention prevents the decrease in oxygen-absorbing ability during storage.
  • processing into packaging materials is possible without foaming.
  • the oxygen-absorbing resin containing the above-described oxygen scavenger is heated and melted at a temperature not lower than the temperature at which the water of crystallization of the metal halide salt contained therein becomes free water, and laminated with another material.
  • the dry storage method of the present invention is applied to the oxygen-absorbing packaging material obtained as described above, the free water derived from the water of crystallization of the metal halide salt and the water adsorbed on the surface of the oxygen-absorbing packaging material are It is removed by the present desiccant.
  • the oxygen-absorbing container obtained by molding such an oxygen-absorbing packaging material when the drying and preservation method of the present invention is applied thereto, adsorbed water adhering to the oxygen-absorbing container becomes the present desiccant. To be removed.
  • the oxygen scavenging container can prevent the oxygen scavenging ability from decreasing during storage.
  • foaming is prevented when the content is filled and then sealed by heat sealing, so that the oxygen-absorbing container package has an impact during distribution. Heat seal strength enough to withstand heat is obtained.
  • the oxygen-absorbing packaging material of the present invention is a film-like or sheet-like packaging material.
  • a film-like thickness is approximately 250 in or less, while a sheet-like thickness is a greater thickness.
  • a deoxidizing container means that there is a risk of quality deterioration due to oxidation.
  • the shape There is no particular limitation on the shape as long as the shape is suitable for filling the container, and the shape may be a cup shape, a tray shape, a bag shape, or the like as appropriate depending on the application.
  • a deoxidizing resin or a deoxidizing packaging material and a desiccant having a moisture absorption substantially equal to or greater than that of a metal halide anhydride of an oxidation promoter are enclosed, and steam barrier packaging is performed.
  • Package in a container a container.
  • a metal can a container of a metal foil laminate such as aluminum foil, a container of an aluminum vapor deposition film laminate, a container of a ceramic vapor deposition film laminate such as sily or alumina are preferably used.
  • the oxygen-absorbing resin or oxygen-absorbing packaging material of the present invention is dried and stored, for example, when a so-called self-reactive oxygen-desorbing sachet is used instead of the desiccant, the oxygen-absorbing resin or oxygen-absorbing packaging material is removed. Although oxygen capacity can be maintained, moisture is transferred from the oxygen scavenger sachet to them, and foaming occurs during thermal processing. Further, as another method, the oxygen in the packaging container for packaging the oxygen-absorbing resin or the oxygen-absorbing packaging material is replaced with an inert gas such as nitrogen to prevent a decrease in the oxygen-absorbing ability during storage. Although it is conceivable, this is not only costly, but also poses a danger of suffocation and other problems in work safety.
  • the dry storage method of the oxygen-absorbing resin or the oxygen-absorbing packaging material of the present invention is low in cost and high in safety as compared with other storage methods, and is easily stored. It is possible to prevent a decrease in the deoxidizing ability and a trouble during the thermoforming or heat sealing. Furthermore, when the desiccant used in the dry preservation method of the present invention is stored in a moisture-permeable or moisture-permeable and heat-resistant bag-like container and used, the oxygen-absorbing resin, the oxygen-absorbing packaging material, and the oxygen-absorbing container Is preferred in terms of workability when dried and stored.
  • Such a moisture-permeable bag-like container is preferably made of a polyethylene film, a polypropylene film, a polyester film, pulp, paper, or a nonwoven fabric of polyethylene or polypropylene.
  • silica gel, zeolite, When synthetic zeolite, activated clay, etc. is used as a desiccant the container for storing it is made of polypropylene film, polyester film, pulp, paper, or non-woven fabric of polypropylene that has both moisture permeability and heat resistance. Is preferred.
  • the desiccant stored in these moisture-permeable and heat-resistant bag-like containers can be reused by heating, vacuum heating, drying under reduced pressure, etc., after subjecting the oxygen-absorbing resin or oxygen-absorbing packaging material to dry storage. Because it becomes.
  • the present inventor has a feature that an oxygen-absorbing laminated package characterized in that it can have an outer layer from the outside, and is composed of an oxygen barrier layer / a nip layer / an oxygen absorbing layer / a sealant layer.
  • an oxygen-absorbing laminated packaging material particularly such a packaging material, having an intermediate layer between the nylon layer and the oxygen-absorbing layer, and a multilayer including an oxygen barrier layer on the entire surface.
  • the oxygen-absorbing laminated packaging material of this prior invention can have an outer layer from the outside, and is composed of an oxygen barrier layer / nylon layer / oxygen absorbing layer / sealant layer. Is an oxygen-absorbing laminated packaging material.
  • the outer layer which can be provided on the outside is not particularly limited, and examples thereof include a material such as polyethylene terephthalate [PET].
  • the thickness of the nylon layer can be set to 3 to 40 m, assuming that the thickness of the entire packaging material of the prior invention is about 200 ⁇ m or less.
  • the oxygen barrier layer is not particularly limited, but is preferably a layer containing at least a metal foil such as aluminum or a metal deposition film.
  • the oxygen absorber any of the conventionally known oxygen absorbers can be used.In particular, iron powder is the main agent, and alkali metal halides such as sodium chloride and calcium chloride or alkali metal halides are used. Those which are used as oxidation promoters are preferred from the viewpoint of hygiene and oxygen absorption capacity.
  • the oxygen absorbing layer can be formed by kneading an oxygen absorbing agent with polyolefin or the like.
  • the material of the sealant layer can also be polyolefin, and the heat seal layer is preferably colored white.
  • such a polyolefin is preferably a polypropylene or a polybutylene copolymer having a propylene content of 70% or more.
  • a three-layered voucher has a four-layered structure when the drop impact strength is insufficient.
  • nylon and polyester are used (edited by the Japan Food Industry Association, “New Edition of the Food Industry General Encyclopedia” (1993, published by Korin Co., Ltd.)).
  • the operation and effect are also different from those of the prior invention.
  • nylon is usually applied to the outside of the barrier layer such as aluminum foil, etc., and there is no previous example of the structure applied to the inside in relation to the deoxidized packaging material.
  • the iron-based oxygen scavenger component increases its particle size due to the generation of mackerel as it absorbs oxygen. In other words, iron powder ( ⁇ ) protrudes from the deoxidizing agent layer.
  • Nylon has a moderate flexibility (the expression “having a waist” is used), and particularly has excellent piercing strength. This prevents overhang.
  • the salt of the oxidation promoter of the iron-based oxygen scavenger gradually migrates through the material during heat treatment or changes over time, and corrodes the metal foil.
  • Nylon has the effect of preventing the migration of salt. Large, thus preventing corrosion. For this reason, applying Nylon internally has the effect of preventing the laminating packaging material from peeling over time. This effect is large, and this effect is particularly remarkable in retort packaging materials, but it can also be applied to ordinary dry matter (such as seasoning granules). It is one of the greatest features of the present invention by the present inventor that the nylon has such an effect in the oxygen-absorbing laminated packaging material.
  • the laminated packaging material of the prior invention is that a plywood layer is provided between a gas barrier layer and an oxygen-absorbing layer.
  • the layer configuration is, for example, PET / AL (aluminum) foil / NY (nylon) It is a laminated material of / oxygen absorption layer / searant layer. This can prevent corrosion of aluminum foil (AL foil) due to migration of additives (calcium chloride, sodium chloride, etc.) in the oxygen absorbing layer (using the barrier property of nylon to salt). Also, when the iron powder oxidizes and expands, it can be prevented from contacting the aluminum foil and corroding the aluminum foil or breaking through the aluminum foil (using the high piercing strength of nylon).
  • Such laminates may have an intermediate layer such as polyolefin between the N Y (nylon) layer and the oxygen absorbing layer.
  • the layer structure in this case is, for example, PET / AL foil / N Y / intermediate layer / oxygen absorbing layer / sealant layer.
  • the polyolefin is also a polypropylene or a polypropylene copolymer having a propylene content of 70% or more, which is the same as described above.
  • the ratio of the thickness of the sealant layer to the thickness of the polyolefin intermediate layer disposed between the nip layer and the oxygen absorbing layer is set to be 1: 0.3 to 1: 2.5.
  • the internal pressure of the oxygen-absorbing layer increases when it is oxidized, and the oxygen-absorbing layer attempts to escape to the inside or outside.
  • the sealant layer is too thin, the oxidation reaction of the oxygen-absorbing layer causes the sealant layer to oxidize. A pinhole is generated at the beginning, and the components of the oxygen absorbing layer are transferred to the contents.
  • the sealant layer is too thick, delamination will occur between the nylon layer and the polyolefin intermediate layer opposite to the sealant layer. Problems can be effectively solved.
  • the oxygen-absorbing packaging material of the prior invention by the present inventor is not only used for making retort descendantss used for making high-quality retort foods, but also as a packaging material. Of course, it can be used for other non-retort bouch applications requiring similar performance.
  • This packaging container is an oxygen-absorbing packaging container characterized in that the entire surface is a multilayer material including an oxygen barrier layer, and at least a part thereof is made of the oxygen-absorbing laminated packaging material described above.
  • the shape is that of a bag.
  • This bag is preferable as a retort pouch (flat bouch, pillow-shaped voucher, standing bouch, etc.), but it is not necessarily limited to a retort pouch, and may be exposed to oxygen or light that does not undergo high-temperature, high-pressure retort treatment. Needless to say, it can be used as a packaging container for foods and other foods that deteriorate in quality. Examples of foods to be contained in the packaging container of the prior invention include foods such as semisolid porridge, solid cooked rice, powdery or granular seasonings, and the like.
  • the oxygen-absorbing laminated packaging material of the prior invention by the present inventor is rarely used for thick packaging materials such as sheets, and is useful for retort enjoyments for retort foods. , That is, about 200 ⁇ m or less.
  • the method for producing a packaging container such as a lettuce voucher using the oxygen-absorbing laminated packaging material of the prior invention is not particularly limited per se, and can be appropriately followed by a conventional method.
  • the oxygen-absorbing packaging material and oxygen-absorbing container to which the dry preservation method of the present invention is applied can be prepared according to the oxygen-absorbing laminated packaging material and the oxygen-absorbing packaging container of the prior invention.
  • a deoxidizing packaging material an oxygen-absorbing laminated packaging material having an oxygen-absorbing layer having a thickness of, for example, 10 to 25 m can be mentioned, and this is particularly preferably used for a retort container. it can.
  • FIG. 1 shows the results of the water content of the oxygen-absorbing resin measured by the Karl Fischer water analysis method immediately after its preparation and after storage in moisture-proof packaging for several days.
  • the solid line is the analysis of the sample immediately after preparation, and the dashed line is the analysis of the sample after several days of storage.
  • the measurement of the water content, the measurement of the oxygen absorption performance, and the evaluation of the film-forming property were performed as follows.
  • test sample deoxygenating resin pellet
  • moisture vaporizer ADP-351 manufactured by Kyoto Electronics Manufacturing Co., Ltd.
  • the moisture was measured using the company's “Karl Fisher Moisture Analyzer MKC-210”.
  • the oxygen-absorbing resin pellet was heated at 180 ° C. under a pressure of 100 kg / cm 2 for 5 minutes to form a sheet of 10 cm ⁇ 10 cm ⁇ 0.5 mm.
  • This sheet Place it in a laminated bag (package container with water vapor barrier) composed of polyethylene terephthalate / A1 foil / polypropylene together with 1 ml of water, adjust the head space air volume to 50 ml, and seal with heat seal. After heating at 66 ° C for 90 minutes, the mixture was allowed to cool for 30 minutes.
  • the oxygen concentration in the head space after heating and cooling was measured by gas chromatography, and the oxygen absorption (oxygen absorption performance) was calculated.
  • Example 1 The state of the film formed by extruding the oxygen-absorbing resin pellet with a thickness of 30 m from a T-die heated to 300 ° C. was observed, and the film forming property was evaluated.
  • Example 1 The state of the film formed by extruding the oxygen-absorbing resin pellet with a thickness of 30 m from a T-die heated to 300 ° C. was observed, and the film forming property was evaluated.
  • Example 3 25 kg of the oxygen-absorbing resin pellet prepared in Example 1 and 50 kg of anhydrous calcium chloride in a desiccant packaged with a moisture-permeable packaging material (polypropylene nonwoven fabric) were mixed with 3 bags of polyethylene / aluminum foil / polyethylene. The bag was placed in a craft paper bag (package container with a water vapor barrier property) and sealed by heat sealing. After storage at room temperature for one month, the physical properties of the deoxygenated resin (water content, oxygen absorption and film forming properties) were evaluated. The results are shown in Table 1 below.
  • Example 3 The results are shown in Table 1 below.
  • Example 4 25 kg of the oxygen-absorbing resin pellet prepared in Example 1 and 50 g of synthetic zeolite (trade name “Zeoram”, manufactured by Tosoh Corporation) are wrapped in a heat- and moisture-permeable packaging material (polypropylene non-woven cloth). The three bags of the desiccant thus obtained were placed in a kraft paper bag containing polyethylene / aluminum foil / polyethylene as an inner bag, and sealed with a heat seal. After storage at room temperature for one month, the physical properties of the deoxidizing resin were evaluated in the same manner as in Example 2. The results are shown in Table 1.
  • Example 4 25 kg of the oxygen-absorbing resin pellet prepared in Example 1 and 50 g of synthetic zeolite (trade name “Zeoram”, manufactured by Tosoh Corporation) are wrapped in a heat- and moisture-permeable packaging material (polypropylene non-woven cloth). The three bags of the desiccant thus obtained were placed in a kraft paper bag containing polyethylene / aluminum foil / polyethylene as an inner bag
  • Example 5 When the weight of the desiccant used for storing the oxygen-absorbing resin in Example 3 was measured, a weight increase of 11 g was recognized.
  • the desiccant contained in the heat-resistant and moisture-permeable packaging material is regenerated by heating at 130 ° C for 2 days under vacuum, and stored in the same manner as in Example 2 using the new deoxidizing resin prepared in Example 1. Later, its physical properties were evaluated. The results are shown in Table 1.
  • Example 6 25 kg of the oxygen-absorbing resin pellet prepared in Example 1 and 50 bags of anhydrous calcium chloride were packaged in a moisture-permeable packing material (polypropylene nonwoven fabric) and 3 bags of a desiccant were deposited on silica-deposited polyethylene terephthalate Z polyethylene. And sealed with a heat seal. After storage at room temperature for one month, the physical properties of the deoxidizing resin were evaluated in the same manner as in Example 2. The results are shown in Table 1.
  • Example 6 25 kg of the oxygen-absorbing resin pellet prepared in Example 1 and 50 bags of anhydrous calcium chloride were packaged in a moisture-permeable packing material (polypropylene nonwoven fabric) and 3 bags of a desiccant were deposited on silica-deposited polyethylene terephthalate Z polyethylene. And sealed with a heat seal. After storage at room temperature for one month, the physical properties of the deoxidizing resin were evaluated in the same manner as in Example 2. The results are shown in Table 1.
  • Polyethylene / aluminum foil / polyethylene were mixed with 25 kg of the oxygen-absorbing resin pellet prepared in Example 7 and 3 bags of desiccant obtained by packing 50 g of anhydrous calcium chloride with a moisture-permeable packaging material (nonwoven polypropylene fabric). It was placed in an inner kraft paper bag and sealed by heat sealing. After storage at room temperature for one month, the dried oxygen-absorbing resin pellets were mixed well with 50 kg of polypropylene resin pellets, and the physical properties were evaluated in the same manner as in Example 2. The results are shown in Table 1. Comparative Example 1
  • Example 2 25 kg of the oxygen-absorbing resin pellet prepared in Example 1 was placed in a kraft paper bag having a polyethylene / aluminum foil / polyethylene inner bag without enclosing a desiccant and sealed with a heat seal. After storage at room temperature for one month, the deoxygenated tree was treated as in Example 2. The physical properties of the fat were evaluated. The results are shown in Table 1. Comparative Example 2
  • Example 2 25 kg of the oxygen-absorbing resin pellet prepared in Example 1 and 3 bags of a self-reactive oxygen absorbent small bag (trade name “Ageless Z-500”, manufactured by Mitsubishi Gas Chemical Co., Ltd.) and polyethylene / A 1 foil / polyethylene inside It was placed in a kraft paper bag and sealed by heat sealing. After storage at room temperature for one month, the physical properties of the deoxidizing resin were evaluated in the same manner as in Example 2. The results are shown in Table 1. Comparative Example 3
  • Example 2 the oxygen-absorbing resin pellets dried and stored in Example 2 were placed between unstretched polypropylene [CPP] (30 jm) and titanium oxide-containing white unstretched polypropylene [CPPw] (30 rn).
  • the deoxidized layer (2) was formed by extruding at 300 ° C from a T-die and sandwich laminating. Subsequently, the CPP surface of the laminate was laminated with a urethane-based adhesive by a usual dry lamination method.
  • Detoxified polyethylene terephthalate [PET] / aluminum foil Deoxygenated laminate by laminating with a urethane-based adhesive using a normal dry laminating method with a stretched nylon (15 mm) nylon surface
  • the obtained oxygen-absorbing packaging material was wound into a roll with a width of 900 mm and a length of 1,000 m ⁇ on a vinyl chloride pipe.
  • Drying agent prepared by packing 50 g of anhydrous calcium chloride with a moisture-permeable packing material (polyethylene non-woven fabric) on both sides of the roll-shaped deoxidizing packing material prepared in Example 9 was placed in each of two bags, and PET / aluminum foil was used. It was packaged with a gum tape using a packaging material made of polypropylene (water vapor barrier property) and stored at room temperature for one month. Was opened one month later, create an inner area that is 3 3 0 cm 2 three-way Shirupauchi, after containing water 1 m 1 in Pauchi, the air amount of dead space to further heat sealed opening 5 0 A four-sided heat seal patch adjusted to ml was prepared.
  • a moisture-permeable packing material polyethylene non-woven fabric
  • Example 1 After storing the roll of the oxygen-absorbing packaging material prepared in Example 9 at room temperature for one month in the same manner as in Example 10 except that no desiccant was used, It was prepared and subjected to oxygen concentration measurement and pressure resistance test in the head space. As a result, the oxygen concentration in the headspace was 6.3%, and the oxygen absorption was 7.8 ml, indicating a decrease in oxygen absorption capacity. In the pressure test, 25 out of 100 bags were broken. Observation of the state of bag breakage revealed that slight foaming was observed in the oxygen-absorbing resin layer in all the heat-sealed portions of the four-side heat sealed pouch.
  • a standing patch was prepared from the deoxidized packaging material prepared in Example 9 (internal area: 330 cm 2 ). Put 2,400 bags of standing pouch and 1 bag of 50 g of anhydrous calcium chloride in a desiccant packed with moisture-permeable packing material (polyethylene non-woven fabric) in a bag made of PET / aluminum foil / polyethylene. And stored at room temperature for 1 month. One month later, the package was opened, 1 ml of water was put in the standing patch, and the opening was heat-sealed to prepare a patch in which the air volume in the head space was adjusted to 50 ml. After the patch was retorted at 121 ° C.
  • Example 12 After storing the standing vouches prepared in the same manner as in Example 11 except that no desiccant was used, the oxygen concentration in the head space was measured in the same manner as in Example 11 after storage as in Example 11 And a pressure test. As a result, the oxygen concentration in the head space was 6.5%, and the oxygen absorption amount was 7.7 ml, indicating a decrease in the oxygen absorption capacity. In the pressure test, 20 bags of 100 bags were broken. When observing the state of bag breakage, slight foaming was observed only in the deoxidized resin layer in the portion that was filled with water in the standing patch and finally heat-sealed.
  • Example 12 Example 12
  • Example 14 25 kg of the oxygen-absorbing resin pellet prepared in Example 12 and 50 g of anhydrous calcium chloride in a desiccant packaged with a moisture-permeable packaging material (polypropylene nonwoven fabric) were mixed with 3 bags of polyethylene / aluminum foil / polyethylene. It was placed in a craft paper bag (steam barrier container) and sealed by heat sealing. After storage at room temperature for one month, the water content of the deoxygenating resin was measured and found to be 250 ppm.
  • a moisture-permeable packaging material polypropylene nonwoven fabric
  • Example 13 The dried oxygen-absorbing resin pellets of Example 13 were extruded at 300 ° C. from a T-die using an extruder on titanium oxide-containing white low-density polyethylene [LD P Ew] (30 m). A deoxygenation layer (20 ⁇ m) was formed to obtain a laminate.
  • the layer structure of this laminate is as follows.
  • the deoxidizing layer (20 m) / LDP Ew (30 m).
  • the PET / aluminum foil stretched nylon (15 zm) laminated with a urethane-based adhesive by a normal dry lamination method and a urethane-based adhesive By dry laminating with the agent, an oxygen-absorbing packaging material as an oxygen-absorbing laminate was obtained.
  • the resulting deoxidized packaging material was wound into a vinyl chloride pipe with a width of 900 mm and a length of 1000 m in a roll.
  • the layer configuration of this laminate is as follows. PET / aluminum foil / stretched nylon (15 m) / deoxidation layer (20 m) / LDPE w (30 m).
  • a roll of oxygen-absorbing wrapping material prepared in Example 14 was placed on both sides with a desiccant packed with 50 g of anhydrous calcium chloride in a moisture-permeable packing material (polyethylene non-woven fabric).
  • PET / aluminum foil / polypropylene It was packaged with a wrapping material (steam barrier property) using gum tape and stored at room temperature for one month.
  • the oxygen concentration of the gas in the patch was measured.
  • the patch after storage for 6 months was visually observed to confirm corrosion of the aluminum foil. The results are shown in Table 2 below. Table 2
  • the deoxidation performance (oxygen absorption performance) is good, and at the same time, the nylon layer is disposed between the aluminum foil, which is a gas barrier layer, and the deoxidizing layer, so that the corrosion of the aluminum foil is reduced.
  • a PET / aluminum foil laminated with a urethane-based adhesive by a usual dry lamination method and dry-laminated with a urethane-based adhesive were used to obtain a deoxidized packaging material as a deoxidized laminate.
  • the obtained oxygen-absorbing packaging material was wound into a vinyl chloride pipe in a roll shape at a width of 900 mm and a length of 1,000 m.
  • the layer structure of this laminate is as follows.
  • Example 16 The same evaluation as in Example 15 was performed for the laminate obtained in Comparative Example 7. The results are also shown in Table 2 above. As shown in this table, the oxygen scavenging ability was good, but the nylon layer was not disposed between the aluminum foil, which is a layer of gas, and the oxygen scavenging layer (oxygen absorbing layer). Temporary corrosion of the aluminum foil was observed.
  • Example 16 The same evaluation as in Example 15 was performed for the laminate obtained in Comparative Example 7. The results are also shown in Table 2 above. As shown in this table, the oxygen scavenging ability was good, but the nylon layer was not disposed between the aluminum foil, which is a layer of gas, and the oxygen scavenging layer (oxygen absorbing layer). Temporary corrosion of the aluminum foil was observed.
  • Example 16 The same evaluation as in Example 15 was performed for the laminate obtained in Comparative Example 7. The results are also shown in Table 2 above. As shown in this table, the oxygen scavenging ability was good, but the nylon layer was not disposed between the aluminum foil,
  • Example 17 An oxygen-absorbing packaging material was obtained in exactly the same manner as in Example 9 except that the thickness of the oxygen-absorbing layer in Example 9 was changed from 2 to 20 m.
  • Example 17 An oxygen-absorbing packaging material was obtained in exactly the same manner as in Example 9 except that the thickness of the oxygen-absorbing layer in Example 9 was changed from 2 to 20 m.
  • Example 9 When the oxygen-absorbing packaging material of Example 16 was used in the same manner as in Example 11, the oxygen concentration was 5.1%, the oxygen absorption amount was 8.3 ml, and the pressure resistance test was all satisfactory. . An opening test was performed from the notch of the standing bouch. But there was no problem. Comparative Example 9
  • Example 9 An oxygen-absorbing packaging material was obtained in exactly the same manner as in Example 9 except that the thickness of the oxygen-absorbing layer in Example 9 was changed from 27 zm to 40 ⁇ m. Comparative Example 1 1
  • Example 17 When the deoxidizing packaging material of Comparative Example 10 was carried out in the same manner as in Example 11, the oxygen concentration was 4.3%, the oxygen absorption amount was 8.7 ml, and all the pressure resistance tests were not problematic. An opening test was conducted from the notch of the standing patch, but it took a considerable amount of force to open.
  • the results of Example 17 and Comparative Example 11 show that even if the thickness of the oxygen-absorbing layer (oxygen-absorbing layer) was doubled, the oxygen-absorbing ability was hardly improved, and the thickness of the oxygen-absorbing layer was 25 / m2. Even with the above thickness, the oxygen scavenger is not effectively used, indicating that the oxygen scavenging ability is hardly improved.
  • the standing patch in Comparative Example 11 had a larger film thickness than that of Example 17, so that the opening property was deteriorated.
  • the oxygen-absorbing packaging material obtained by laminating the same with other materials, and the method for drying and storing an oxygen-absorbing container prepared using this packaging material, Moisture absorption by the metal halide salt used as an accelerator is prevented, which in turn prevents a decrease in the oxygen-absorbing capacity during storage, and furthermore, the oxygen-absorbing resin or the oxygen-absorbing packaging material is used as it is.
  • the oxygen-absorbing resin or the oxygen-absorbing packaging material is used as it is.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Packages (AREA)

Abstract

L'invention concerne un procédé destiné au séchage et au stockage d'une résine désoxygénante ou d'une matière de conditionnement désoxygénante. Ce procédé se caractérise en ce qu'une résine désoxygénante renfermant un agent désoxygénant comprenant de la poudre de fer et un sel haloïde métallique, une matière de conditionnement désoxygénante obtenue par stratification de la résine désoxygénante et d'une autre matière, ou un récipient désoxygénant fabriqué au moyen de cette matière de conditionnement désoxygénante subit un traitement thermique à une température de 20 °C ou plus supérieure à la température de libération de l'eau cristalline du sel haloïde métallique, lequel se trouve à une température impliquant la libération de cette eau cristalline, d'où la formation d'un sel sensiblement anhydre. Ensuite, la matière de conditionnement ou le récipient est stocké dans un état d'étanchéité conjointement avec un agent de séchage présentant une capacité d'absorption d'humidité sensiblement égal ou supérieur à celui du sel anhydre issu du sel haloïde métallique dans un récipient de conditionnement doté de propriétés d'étanchéité à l'humidité. Ce procédé permet d'empêcher sans difficulté que la capacité désoxygénante de cette résine désoxygénante, de cette matière de conditionnement désoxygénante ou de ce récipient désoxygénant ne diminue en cours de stockage. Il permet également de les empêcher de mousser lorsqu'ils sont soumis à une opération de thermoformage ou de thermoscellage.
PCT/JP1999/007316 1999-12-27 1999-12-27 Procede de sechage et de stockage de resine desoxygenante ou de matiere de conditionnement desoxygenante WO2001048064A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PCT/JP1999/007316 WO2001048064A1 (fr) 1999-12-27 1999-12-27 Procede de sechage et de stockage de resine desoxygenante ou de matiere de conditionnement desoxygenante

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP1999/007316 WO2001048064A1 (fr) 1999-12-27 1999-12-27 Procede de sechage et de stockage de resine desoxygenante ou de matiere de conditionnement desoxygenante

Publications (1)

Publication Number Publication Date
WO2001048064A1 true WO2001048064A1 (fr) 2001-07-05

Family

ID=14237703

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP1999/007316 WO2001048064A1 (fr) 1999-12-27 1999-12-27 Procede de sechage et de stockage de resine desoxygenante ou de matiere de conditionnement desoxygenante

Country Status (1)

Country Link
WO (1) WO2001048064A1 (fr)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02203937A (ja) * 1989-02-02 1990-08-13 Sumitomo Chem Co Ltd 自力反応型酸素吸収シートの製造方法
JPH053776A (ja) * 1990-10-15 1993-01-14 Mitsubishi Gas Chem Co Inc 加熱処理食品包装体
WO1996040412A2 (fr) * 1995-06-07 1996-12-19 Amoco Corporation Compositions piegeant l'oxygene
JPH09173831A (ja) * 1995-12-23 1997-07-08 Sony Corp 脱酸素材料及びその製造方法
JPH1028860A (ja) * 1996-07-18 1998-02-03 Sony Corp 脱酸素剤及びその製造方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02203937A (ja) * 1989-02-02 1990-08-13 Sumitomo Chem Co Ltd 自力反応型酸素吸収シートの製造方法
JPH053776A (ja) * 1990-10-15 1993-01-14 Mitsubishi Gas Chem Co Inc 加熱処理食品包装体
WO1996040412A2 (fr) * 1995-06-07 1996-12-19 Amoco Corporation Compositions piegeant l'oxygene
JPH09173831A (ja) * 1995-12-23 1997-07-08 Sony Corp 脱酸素材料及びその製造方法
JPH1028860A (ja) * 1996-07-18 1998-02-03 Sony Corp 脱酸素剤及びその製造方法

Similar Documents

Publication Publication Date Title
JP3171259B2 (ja) 酸素吸収剤
US6596191B2 (en) Oxygen absorbing composition, oxygen absorbing resin composition using the oxygen absorbing composition, and preserving method utilizing these compositions
US6133361A (en) Oxygen-absorbing composition, oxygen-absorbing resin composition, packing material, multi-layered packing, oxygen absorber packet, packing method and preservation method
JP4019339B2 (ja) 炭酸ガス吸収積層体、これを用いた容器及び食品類の保存方法
JPH0826348A (ja) 湿度調節積層袋
JP2003088344A (ja) 酸素吸収及び炭酸ガス吸収多層体
JP3282567B2 (ja) 活性化型酸素吸収剤を含む包装用積層体
WO2001048064A1 (fr) Procede de sechage et de stockage de resine desoxygenante ou de matiere de conditionnement desoxygenante
EP1842794B1 (fr) Emballage de fromage
JP3788057B2 (ja) 脱酸素樹脂組成物、脱酸素包装材料及びこれらを用いる脱酸素容器の乾燥保存方法
JP3246538B2 (ja) 蓋用パッキング
JP4131030B2 (ja) 脱酸素剤組成物、脱酸素剤包装体および物品の保存方法
JP2002052655A (ja) 酸素吸収性多層体及びこれを用いた低水分含有物品の保存方法
US20050034599A1 (en) Oxygen absorber composition, oxygen absorber packaging and oxygen absorption method
JP4085218B2 (ja) 脱酸素剤組成物及び保存方法
JP4174633B2 (ja) 酸素吸収性積層包装材料
JP3376915B2 (ja) 脱酸素性多層体、これを用いた包装容器、及び食品又は医薬品の保存方法
JP2666381B2 (ja) 脱酸素剤用包装フィルム
JP2000142815A (ja) 脱酸素性密封包装容器および保存方法
JP2002284216A (ja) 脱酸素機能を有する蓋
JP4544377B2 (ja) 酸素吸収性多層体
JP3246537B2 (ja) 蓋用パッキング
JP7383897B2 (ja) 炭酸ガス調整積層体と包装体
JPH1044333A (ja) 乾燥食品用包材および乾燥食品の包装方法
WO2023182130A1 (fr) Composition de piégeage d'oxygène, boîtier de piégeage d'oxygène et procédé de fabrication d'un boîtier de piégeage d'oxygène

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): US

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
122 Ep: pct application non-entry in european phase