JPH0429840A - Gas permeable packaging material and packaged body therewith - Google Patents
Gas permeable packaging material and packaged body therewithInfo
- Publication number
- JPH0429840A JPH0429840A JP13411990A JP13411990A JPH0429840A JP H0429840 A JPH0429840 A JP H0429840A JP 13411990 A JP13411990 A JP 13411990A JP 13411990 A JP13411990 A JP 13411990A JP H0429840 A JPH0429840 A JP H0429840A
- Authority
- JP
- Japan
- Prior art keywords
- packaging material
- synthetic resin
- film
- breathable
- resin
- Prior art date
- 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.)
- Pending
Links
- 239000005022 packaging material Substances 0.000 title claims abstract description 44
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 30
- 239000000057 synthetic resin Substances 0.000 claims abstract description 30
- 239000011148 porous material Substances 0.000 claims abstract description 27
- 230000035699 permeability Effects 0.000 claims abstract description 26
- 238000000034 method Methods 0.000 claims abstract description 24
- 239000004745 nonwoven fabric Substances 0.000 claims abstract description 21
- -1 polyethylene Polymers 0.000 claims abstract description 21
- 239000000463 material Substances 0.000 claims abstract description 15
- 239000004698 Polyethylene Substances 0.000 claims abstract description 8
- 239000004743 Polypropylene Substances 0.000 claims abstract description 8
- 229920000573 polyethylene Polymers 0.000 claims abstract description 8
- 229920001155 polypropylene Polymers 0.000 claims abstract description 8
- 229920005672 polyolefin resin Polymers 0.000 claims abstract description 7
- 239000000945 filler Substances 0.000 claims abstract description 5
- 229920005989 resin Polymers 0.000 claims description 31
- 239000011347 resin Substances 0.000 claims description 31
- 238000002844 melting Methods 0.000 claims description 26
- 230000008018 melting Effects 0.000 claims description 26
- 239000012982 microporous membrane Substances 0.000 claims description 22
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 12
- 239000007787 solid Substances 0.000 claims description 10
- 238000004806 packaging method and process Methods 0.000 claims description 8
- 229910010272 inorganic material Inorganic materials 0.000 claims description 7
- 239000011147 inorganic material Substances 0.000 claims description 7
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 6
- 229920006026 co-polymeric resin Polymers 0.000 claims description 6
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 6
- 239000000835 fiber Substances 0.000 claims description 6
- 229920000554 ionomer Polymers 0.000 claims description 6
- 238000009987 spinning Methods 0.000 claims description 6
- 229920006122 polyamide resin Polymers 0.000 claims description 5
- 229920006228 ethylene acrylate copolymer Polymers 0.000 claims description 4
- 229920005648 ethylene methacrylic acid copolymer Polymers 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 229920000098 polyolefin Polymers 0.000 claims description 2
- 238000005538 encapsulation Methods 0.000 claims 1
- 238000000605 extraction Methods 0.000 abstract description 2
- 239000010408 film Substances 0.000 description 27
- 238000007789 sealing Methods 0.000 description 11
- 239000004831 Hot glue Substances 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 239000002274 desiccant Substances 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 239000012943 hotmelt Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000001877 deodorizing effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229920003298 Nucrel® Polymers 0.000 description 1
- 229940123973 Oxygen scavenger Drugs 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 108010081750 Reticulin Proteins 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000007791 dehumidification Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
Landscapes
- Bag Frames (AREA)
- Wrappers (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、乾燥剤、脱湿剤、脱酸素剤、鮮度維持剤、脱
臭剤、芳香剤等の新規な包材及びそれからの包体に関す
る。Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a novel packaging material for desiccants, desiccants, oxygen scavengers, freshness-preserving agents, deodorizing agents, fragrances, etc., and packages thereof. .
(従来の技術)
通気性または透湿性を必要とする包材、例えば塩化カル
シウムを脱湿剤とする家庭用品、あるいは食品等の保存
に用いられる脱酸素剤等の包材は、従来、ポリエチレン
、ポリプロピレンなとのポリオレフィン系樹脂に炭酸カ
ルシウム、微細フィラー等の無機質材を混ぜて薄い膜状
に形成し、該無機質材を取り除いた微多孔膜、またはポ
リエチレンなどのポリオレフィン系樹脂のフラッシュ・
スピニング法により得られた網状繊維の積層物を熱ロー
ル圧着させて得られた微多孔を有する不織布状物に、■
球形状又は粉体状ホットメルト接着剤の分散液のコー
テング、あるいは■ 針状物などで孔をあけたホットメ
ルト樹脂製フィルムの熱融着面を包材として使用してい
る。(Prior Art) Packaging materials that require air permeability or moisture permeability, such as household products that use calcium chloride as a desiccant agent, or packaging materials for oxygen absorbers used to preserve foods, etc., have conventionally been made of polyethylene, Microporous membranes made by mixing inorganic materials such as calcium carbonate and fine fillers with polyolefin resins such as polypropylene to form a thin film, and removing the inorganic materials, or flash films made from polyolefin resins such as polyethylene.
A microporous nonwoven fabric obtained by hot roll compression bonding of a laminate of reticular fibers obtained by a spinning method,
Coating with a dispersion of spherical or powdered hot melt adhesive, or (2) The heat-sealing surface of a hot melt resin film with holes made with a needle or the like is used as the packaging material.
■の方法においては、球形状又は粉体状ホットメルト接
着剤の分散液のコーテング後、熱風により乾燥を行うが
、温度、時間、風量の僅がの変動により該ホットメルト
接着剤の溶融程度が異なってくるために、通気性徴多孔
膜もしくは不織布状物の通気性を任意の範囲に規制する
ことは非常に困難である。In method (2), after coating with a dispersion of spherical or powder hot melt adhesive, drying is performed with hot air, but slight fluctuations in temperature, time, and air volume may affect the degree of melting of the hot melt adhesive. Therefore, it is very difficult to control the air permeability of a porous membrane or nonwoven fabric to a desired range.
さらに、低温、短時間の乾燥では該ホットメルト接着剤
は溶融せず、微多孔膜または不織布状物よりホットメル
ト接着剤が容易に剥離・脱落し、また僅かの昇温にて該
球形状又は粉体状のホットメルト接着剤の形状が崩れ、
微多孔膜もしくは不織布状物の微孔を埋め、通気性を極
端に低下させる。Furthermore, the hot melt adhesive does not melt when drying at a low temperature for a short time, and easily peels off and falls off from the microporous membrane or nonwoven fabric. The powdered hot melt adhesive loses its shape,
It fills the pores of a microporous membrane or non-woven material, drastically reducing its air permeability.
■の方法においては、例えば実願昭55−89576号
に記載されているように、包材強度の補充のために、ホ
ットメルト性有孔フィルムを熱融着させる方法では、フ
ィルムに多数の孔をあけることによりフィルムの強度は
低下し、また、大きな孔をあければ、包材となした後の
熱融着面の強度低下又は包体内の粉剤等の漏れを生じる
。また、フィルムに小孔を少数あければ、微多孔膜もし
くは不織布状物の通気性、透湿性を阻害し、目的とする
包材が得難い。In the method (2), for example, as described in Utility Model Application No. 55-89576, in order to supplement the strength of the packaging material, a hot-melt perforated film is heat-sealed. By making holes, the strength of the film decreases, and if large holes are made, the strength of the heat-sealed surface after being made into a packaging material decreases, or the powder, etc. inside the package may leak. Furthermore, if a small number of pores are formed in the film, the air permeability and moisture permeability of the microporous membrane or nonwoven fabric will be inhibited, making it difficult to obtain the desired packaging material.
(発明が解決しようとする課題)
本発明は、上記従来技術の問題点である、ホットメルト
接着剤(c)による微多孔膜もしくは不織布状物(a)
の通気性低下及び通気性の制御、または小孔、少数孔の
ホットメルト性有孔フィルム(c)による微多孔膜もし
くは不織布状物(a)の通気性低下を解決しようとする
ものである。(Problems to be Solved by the Invention) The present invention solves the problems of the above-mentioned prior art by using a microporous membrane or a nonwoven fabric (a) using a hot melt adhesive (c).
The purpose of this invention is to solve the problem of reducing the air permeability of a microporous membrane or nonwoven fabric (a) due to the hot-melt perforated film (c) having small or few holes.
(課題を解決するための手段)
前記の従来技術の問題点を解決するために、本発明は;
■ (a) 孔径50μ以下で、ガーレ法通気度が0
.1〜10,000秒/ 100 ccである微多孔膜
もしくは不織布状物と、
(b)、(a)より融点が低く、通気性を有する有孔の
合成樹脂製フィルムとの間に、
(c)、(ロ)より融点が低い合成樹脂を部分的に位置
せしめ、(a)と(c)、(c)と0))を接着してな
る(a)、(b)、(c)の一体の通気性包材を提供す
る。また、■ 上記通気性包材の全部又は一部を使用し
、(a)面を外面として内部に固体を包含させ、周囲を
熱融着し、当該固体が漏洩しないようになした通気性包
体をも提供する。(Means for Solving the Problems) In order to solve the problems of the prior art described above, the present invention provides:
.. 1 to 10,000 seconds/100 cc and a perforated synthetic resin film having a lower melting point than (b) and (a) and having air permeability, (c ), (b), where a synthetic resin with a lower melting point than that of (b) is partially placed, and (a) and (c), (c) and 0)) are bonded together (a), (b), and (c). Provides an integrated breathable packaging material. In addition, (1) A breathable packaging using all or part of the above-mentioned breathable packaging material, with the (a) side as the outer surface, containing a solid inside, and heat-sealing the periphery to prevent the solid from leaking. He also provides his body.
さらに、本発明は;
■ 上記微多孔膜もしくは不織布状物(a)が、炭酸カ
ルシウム、微細フィラー等の無機質材をブレンドしてな
るポリエチレン、ポリプロピレン等のポリオレフィン系
樹脂フィルムから該無機質材の除去により得られる微多
孔膜、またはフラッシュ・スピニング法により得られた
ポリオレフィン系繊維の積層物である点にも、また、
■ 上記合成樹脂製フィルム(ト))、合成樹脂(c)
が、ポリエチレン、エチレン−酢酸ビニル系共重合樹脂
、エチレン−アクリレート系共重合樹脂、エチレン−メ
タクリル酸系共重合樹脂、アイオノマー樹脂、ポリアミ
ド樹脂及びこれらの変性樹脂または前記樹脂の2種以上
の混合物からなる群から選ばれた材料である点にも、ま
た
■ 上記合成樹脂(c)が、点状に、又は(a)面に平
行な線状又は格子状に位置している点にも特徴がある。Furthermore, the present invention provides: (1) The microporous membrane or nonwoven fabric material (a) is obtained by removing the inorganic material from a polyolefin resin film such as polyethylene or polypropylene blended with an inorganic material such as calcium carbonate or a fine filler. The microporous membrane obtained is also a laminate of polyolefin fibers obtained by a flash spinning method.
is made from polyethylene, ethylene-vinyl acetate copolymer resin, ethylene-acrylate copolymer resin, ethylene-methacrylic acid copolymer resin, ionomer resin, polyamide resin, modified resins thereof, or mixtures of two or more of the above resins. It is also characterized by the fact that the synthetic resin (c) is arranged in dots, or in the form of lines or grids parallel to the plane (a). be.
以下、本発明の詳細な説明する。The present invention will be explained in detail below.
本発明における微多孔膜(a)は、炭酸カルシウム、微
細フィラー等の無機質材などを混入したポリエチレン、
ポリプロピレン等のポリオレフィン系樹脂を常法に従っ
て製膜した後、該無機質材を抽出法などの手段により除
去した、通気性微多孔膜である。The microporous membrane (a) in the present invention includes polyethylene mixed with inorganic materials such as calcium carbonate and fine fillers;
This is an air-permeable, microporous membrane in which a polyolefin resin such as polypropylene is formed into a membrane according to a conventional method, and then the inorganic material is removed by means such as an extraction method.
また、本発明における不織布状物(a)とは、ポリエチ
レン、ポリプロピレン等のポリオレフィン系樹脂を主体
とした樹脂原料からフラッシュ・スピニング法にて得ら
れた三次元網状繊維の積層体を、該樹脂原料の融点近辺
の温度の熱ロールにて、部分的に繊維間を自己融着させ
て得られた通気性不織布状物である。In addition, the nonwoven fabric (a) in the present invention refers to a laminate of three-dimensional network fibers obtained by a flash spinning method from a resin raw material mainly composed of polyolefin resins such as polyethylene and polypropylene. This is an air-permeable nonwoven fabric obtained by partially self-fusing the fibers using a heated roll at a temperature close to the melting point of .
本発明に使用される微多孔膜もしくは不織布状物(a)
は、孔径50μ以下、好ましくは20μ以下である。孔
径が50μより大であると、包材内部の固体が粉剤であ
る場合に漏洩の危険がある。特に、孔径20μ以下の場
合は、粉剤が例えば塩化カルシウムの如き吸湿剤を用い
る時に、吸湿・潮解後、包材よりの液浸出防止に有効と
なり好ましい。Microporous membrane or nonwoven fabric used in the present invention (a)
has a pore diameter of 50μ or less, preferably 20μ or less. If the pore size is larger than 50μ, there is a risk of leakage if the solid inside the packaging material is powder. In particular, when the pore size is 20 μm or less, it is effective in preventing liquid leaching from the packaging material after moisture absorption and deliquescence when the powder uses a moisture absorbent such as calcium chloride.
また、ガーレ法通気度が0.1〜10,000秒/ 1
00 cc、好ましくは1〜5.000秒/100cc
である。0.1秒/ 100 cc以上では、包材内部
の固体が粉剤である場合に漏洩の危険があり、固体が香
料等の液体を含浸させた繊維質の場合も液体の浸出の危
険がある。また、10,000秒/ 100 cc以上
の場合は、通気度が低く、本発明の目的にそぐわない。In addition, the Gurley method air permeability is 0.1 to 10,000 seconds/1
00 cc, preferably 1-5.000 seconds/100cc
It is. At 0.1 seconds/100 cc or more, there is a risk of leakage if the solid inside the packaging material is a powder, and there is also a risk of liquid leaching if the solid is fibrous material impregnated with a liquid such as perfume. In addition, if it is 10,000 seconds/100 cc or more, the air permeability is low and is not suitable for the purpose of the present invention.
本発明における合成樹脂製フィルム(b)または(c)
は、ポリエチレン、エチレン−酢酸ビニル系共重合樹脂
、エチレン−アクリレート系共重合樹脂、エチレン−メ
タクリル系共重合樹脂、アイオノマ−樹脂、ポリアミド
樹脂及びこれらの変性樹脂または前記樹脂の2種以上の
混合物からなる群から選ばれた材料から構成され、粘着
付与剤、可塑剤、酸化防止剤など公知の添加剤を含有し
ていてもよい。Synthetic resin film (b) or (c) in the present invention
is polyethylene, ethylene-vinyl acetate copolymer resin, ethylene-acrylate copolymer resin, ethylene-methacrylic copolymer resin, ionomer resin, polyamide resin, modified resins thereof, or mixtures of two or more of the above resins. It is made of a material selected from the group consisting of: and may contain known additives such as a tackifier, a plasticizer, and an antioxidant.
ここで、これらの変性樹脂とは、ポリエチレン、エチレ
ン−酢酸ビニル系共重合樹脂、エチレンアクリレート系
共重合樹脂、エチレン−メタクリル系共重合樹脂、アイ
オノマー樹脂については、これらの樹脂に他のオレフィ
ン性化合物を(グラフ日共重合したり又は他の共重合性
官能性化合物を(グラフト)共重合したり、官能性化合
物で変性した樹脂であり、あるいはポリアミド樹脂につ
いては、ポリアミドイミドなどのように、他の縮合性モ
ノマーなどを共縮合させて変性した樹脂であり、それ自
体公知のこれらの変性樹脂を包含する。Here, these modified resins include polyethylene, ethylene-vinyl acetate copolymer resin, ethylene acrylate copolymer resin, ethylene-methacrylate copolymer resin, and ionomer resins that contain other olefinic compounds. It is a resin that is copolymerized (grafted) or (grafted) with other copolymerizable functional compounds, or modified with a functional compound, or for polyamide resins, it is a resin that is modified with other copolymerizable functional compounds, such as polyamideimide, etc. It is a resin modified by co-condensing condensable monomers, etc., and includes these modified resins that are known per se.
本発明に使用される合成樹脂フィルム(b)の孔の形成
の方法はとくに制限されないが、針布を用い機械的にあ
けるか、あるいは合成樹脂フィルム(b)の融点以上に
熱せられた針先端に接触・融解させる方法等を挙げるこ
とができ、種々の任意の方法が採用され得る。The method for forming holes in the synthetic resin film (b) used in the present invention is not particularly limited, but may be formed mechanically using a cloth, or by heating the tip of a needle to a temperature higher than the melting point of the synthetic resin film (b). Examples include a method of contacting and melting the material, and various arbitrary methods may be employed.
合成樹脂フィルム(b)の孔の大きさは特に規定されな
いが、その孔径が大きい場合には、包材となすに当たっ
て、その孔の部分がヒートシール部となる時に、ヒート
シール後の剥離強力の低下を招き易く、また孔径がより
小さければ、目的とする通気性のある包材が得がたい。The size of the pores in the synthetic resin film (b) is not particularly specified, but if the pores are large, the peel strength after heat sealing may be If the pore size is smaller, it is difficult to obtain the intended packaging material with air permeability.
好ましくは0.2〜2mmφが良い。Preferably, the diameter is 0.2 to 2 mm.
さらに、合成樹脂フィルム(b)の孔の大きさは、微多
孔膜もしくは不織布状物(a)のそれより大きくするこ
とが、空気抵抗性及び得られた包材の通気性の点から好
ましい。従って、上記のように機械的にまたは熱融解に
より孔が開けられた有孔の合成樹脂フィルムを好ましく
使用できる。Furthermore, it is preferable that the pore size of the synthetic resin film (b) be larger than that of the microporous membrane or nonwoven material (a) from the viewpoint of air resistance and air permeability of the resulting packaging material. Therefore, a perforated synthetic resin film in which holes are made mechanically or by thermal melting as described above can be preferably used.
また、合成樹脂フィルム(b)の孔数は、少なければ通
気性のある包材が得がたく、多ければ強度に欠け、加工
し難い。好ましくは、1〜10ケ/ crRが良い。Furthermore, if the number of holes in the synthetic resin film (b) is small, it is difficult to obtain a breathable packaging material, and if it is large, it lacks strength and is difficult to process. Preferably, it is 1 to 10 pieces/crR.
合成樹脂フィルム(b)の孔径、孔数は、微多孔膜もし
くは不織布状物(a)の通気度、及び包材となすに当た
って必要とする目的の通気度に従って容易に決定し得る
。The pore diameter and number of pores of the synthetic resin film (b) can be easily determined according to the air permeability of the microporous membrane or nonwoven fabric (a) and the desired air permeability required for use as a packaging material.
合成樹脂製フィルム(ロ)の融点は、微多孔膜もしくは
不織布状物(a)より低く、5℃以上低いのが好ましい
。The melting point of the synthetic resin film (b) is lower than that of the microporous membrane or nonwoven fabric material (a), preferably 5° C. or more lower.
合成樹脂(c)の融点は、合成樹脂製フィルム(b)よ
り低く、5℃以上低いのが好ましい。The melting point of the synthetic resin (c) is lower than that of the synthetic resin film (b), preferably 5° C. or more lower.
本発明は、微多孔膜もしくは不織布状物(a)と合成樹
脂製フィルム(b)の間に、部分的に配置した合成樹脂
(c)を介在させて、(a)と(b)とを直接に接着さ
せないことが必要である。このようにして(a)、(ロ
)、(c)を一体化するには、(c)面を融解するが、
(a)、(ロ)を融解せずに熱融着させるために、各(
a)、(b)、(c)の融点間に5℃以上の温度差を有
することが好ましい。In the present invention, a partially disposed synthetic resin (c) is interposed between a microporous membrane or a non-woven fabric (a) and a synthetic resin film (b) to combine (a) and (b). It is necessary not to bond directly. In order to integrate (a), (b), and (c) in this way, the (c) side must be melted, but
In order to thermally fuse (a) and (b) without melting, each (
It is preferable that there is a temperature difference of 5° C. or more between the melting points of a), (b), and (c).
本発明における通気性包材を包体となすには、(b)面
を内面として内部に固体を包含させて周囲を熱融着させ
る際に、(a)面よりヒートシールバー等により熱圧着
させる場合、(a)面に融解等の損傷を与えず、(a)
、(c)、(b)、(b)、(c)、(a)の順に熱融
着、あるいは(a)、(c)、(b)、(他の素材)の
順に熱融着させる場合にも、微多孔膜もしくは不織布状
物(a)より合成樹脂製フィルムし)の方の融点が10
°C以上低いのがより好ましい。In order to make the breathable packaging material of the present invention into a package, when the surface (b) is the inner surface and the solid is contained inside and the surroundings are heat-sealed, the material is thermally compressed from the surface (a) using a heat seal bar or the like. (a) without causing damage such as melting to the (a) side.
, (c), (b), (b), (c), (a) in this order, or (a), (c), (b), (other materials) in this order. In this case, the melting point of the microporous membrane or nonwoven material (a) is higher than that of the synthetic resin film (a).
It is more preferable that the temperature is lower than °C.
本発明において、(a)と(ロ)間への(c)の部分的
位置付けは、拡布されて走行する(a)面上に粉体(球
形状も含む)である(c)を散布する方法や、アプリケ
ーターにて熱溶融された(c)の圧空により間歇ジェッ
トによる、(a)面または(b)面へのトッド状付与や
その連続噴霧、線状噴霧、あるいはグラビアロールによ
る点状、線状または格子状付与など何れの方法でもよく
、(c)の(a)面または(ロ)面への付与後、(a)
面とΦ)面とが接着しないように、熱風又は熱ローラー
等の適当な熱媒体により(c)表面を熱溶融させ、必要
に応じて圧着するなどして(a)と(c)、(c)と(
ロ)との間の熱接着で(a)、(c)、(b)の一体化
が行われる。In the present invention, the partial positioning of (c) between (a) and (b) means that (c), which is a powder (including spherical shape), is scattered on the surface of (a) that is spread and travels. Methods include applying a tod-like shape to the (a) surface or (b) surface by intermittent jetting using the pressurized air of (c) heated by an applicator, continuous spraying, linear spraying, or dot-like application using a gravure roll, Any method such as linear or grid-like application may be used, and after applying to the (a) side or (b) side of (c), (a)
(a), (c), ( c) and (
(a), (c), and (b) are integrated by thermal bonding between (b) and (b).
上述した方法により得られた通気性包材は、(a)を外
面にして、縦型又は横型ピロータイプの包装機又は他の
包装機を使用して、脱臭剤、防虫剤等の薬剤を充填し、
ヒートシールを行う。The breathable packaging material obtained by the above method is filled with chemicals such as deodorizers and insect repellents using a vertical or horizontal pillow type packaging machine or other packaging machine with (a) as the outer surface. death,
Heat seal.
ヒートシールには、バーシール、インパルスシール、超
音波シール等積々の方法が用いられる。A variety of methods are used for heat sealing, including bar sealing, impulse sealing, and ultrasonic sealing.
温度、圧力、時間等のヒートシール条件は、(a)、(
b)、(c)の素材の熱特性により、または本発明の通
気性包材の部分的使用の場合には、他の素材の熱特性な
どをも考慮して、適宜決定され得る。Heat sealing conditions such as temperature, pressure, time, etc. are (a), (
It can be determined as appropriate depending on the thermal properties of the materials b) and (c), or in the case of partial use of the breathable packaging material of the present invention, also taking into consideration the thermal properties of other materials.
このようにして、本発明の通気性包体が得られる。In this way, the breathable packaging of the present invention is obtained.
(作用)
従来方法、即ち(a)と(ロ)が直接に接着してなる通
気性包材の場合、第4図に示されるように、孔部1に接
するa部分のみ通気性となり、全体的には通気性が減少
する。(Function) In the case of the conventional method, that is, in the case of a breathable packaging material made by directly adhering (a) and (b), only the part a in contact with the hole 1 becomes breathable, as shown in FIG. In other words, air permeability decreases.
しかるに、本発明の通気性包材の場合、第1図に示され
るように、a部分とb部分が直接に接しておらずにC部
分を介しているために、b部分の孔部1を通過する気体
はa部分とb部分間を自由に移動し、C部分を除いたa
部分の全面に亘る通気性を享受し得る。However, in the case of the breathable packaging material of the present invention, as shown in FIG. The passing gas moves freely between parts a and b, and
You can enjoy breathability over the entire area.
すなわち、b部分の孔数が少なく、かっ孔径を小さくし
ても、微多孔膜または不織布状物(a)の孔径に比較し
て、例えば機械的または熱融解等の方法によりあけられ
た孔であるために大きく、しかも孔の空気抵抗は低い故
に、本発明の構成からなる包材は、従来方法により得ら
れた包材よりも通気性がある。In other words, even if the number of pores in part b is small and the pore diameter is small, the pores made by mechanical or thermal melting methods, for example, are smaller than the pore diameter of the microporous membrane or nonwoven fabric (a). Because of the large size and low air resistance of the pores, packaging materials constructed according to the invention are more breathable than packaging materials obtained by conventional methods.
次に、この包材を部分的に使用しく第2図)、またはこ
の包材の全部を使用しく第3図)、b面を内面にして固
体を入れ、周囲を熱融着してヒートシール部2を形成す
る。熱融着の際に、周囲のヒートシール部2を圧するこ
とにより微量のCは融解し、全面にある多量のb中に埋
没し、隙間なく内部の固体は封印される。しかも、周囲
のヒートシール部2以外は熱圧着の影響を受けず、本発
明の包材と同様に通気性を有したままである。Next, use this packaging material partially (see Figure 2) or use the entire packaging material (see Figure 3), place the solid with the b side facing inside, and heat seal by heat-sealing the surrounding area. Form part 2. During thermal fusion, a small amount of C is melted by pressing the surrounding heat-sealed portion 2 and is buried in a large amount of B on the entire surface, sealing the solid inside without any gaps. Moreover, the parts other than the surrounding heat-sealed part 2 are not affected by the thermocompression bonding and remain breathable like the packaging material of the present invention.
以下、本発明を実施例及び比較例を挙げて説明するが、
これらは本発明の範囲を制限しない。The present invention will be explained below with reference to Examples and Comparative Examples.
These do not limit the scope of the invention.
(実施例1)
フラッシュ・スピニング法により得られたポリエチレン
の三次元網状繊維の積層体を137°Cの熱ロールにて
熱圧着し、最大孔径7μ、平均孔径3μ、ガーレ法通気
度20秒/ 100 cc、坪量50g/ポ、厚み16
0μ、融点138°Cの不織布状物(a、)(旭化成工
業■製、ルクサーH@)を得た。(Example 1) A laminate of three-dimensional network fibers of polyethylene obtained by the flash spinning method was thermocompressed using a hot roll at 137°C, and the maximum pore diameter was 7μ, the average pore diameter was 3μ, and the Gurley method air permeability was 20 seconds/ 100 cc, basis weight 50g/po, thickness 16
A non-woven fabric (a,) (manufactured by Asahi Kasei Kogyo ■, Luxar H@) was obtained.
ロール状に巻かれた(a、)を拡げ、(al)上にエチ
レン−酢酸ビニル共重合樹脂を主体とした融点85°C
1直径220μの粉状樹脂(c1)(旭化成工業■製、
PAK−X309@)を7g/ITfで散布し、次いで
、エチレン−酢酸ビニル共重合樹脂を主体とした融点9
3°C1厚み25μ、孔径1am+φ、孔数1ケ/dの
フィルム(b、)(三井石油化学工業■製、エバフレッ
クス[F]より作成)を(c+)上に重ね、90°Cに
熱せられた金属ロールとゴムロールの間を通過させ、(
c+)の表面層のみを融解させ、(al)と(c)、(
c3)と(bl)を熱融着させた。The rolled (a,) is spread out, and a layer of ethylene-vinyl acetate copolymer resin (melting point 85°C) is placed on (al).
1. Powdered resin (c1) with a diameter of 220μ (manufactured by Asahi Kasei Kogyo ■,
PAK-X309@) was sprayed at 7g/ITf, and then a melting point of 9 containing mainly ethylene-vinyl acetate copolymer resin was applied.
A film (b, ) (manufactured by Mitsui Petrochemical Industries ■, made from Evaflex [F]) with a thickness of 25μ, a pore diameter of 1am + φ, and a number of holes of 1/d was placed on top of (c+) at 3°C and heated to 90°C. Pass it between the metal roll and rubber roll,
By melting only the surface layer of (c+), (al), (c), (
c3) and (bl) were thermally fused.
(比較例1)
実施例1において、(c1)を使用せず、(aI)と(
bl)を重ね、95℃に熱せられた金属ロールとゴムロ
ールの間を通過させ、(al)と(bl)を接着させた
。短時間通過のため、(bl)の孔度化はなかった。(Comparative Example 1) In Example 1, (c1) was not used, and (aI) and (
bl) were stacked and passed between a metal roll and a rubber roll heated to 95°C to bond (al) and (bl). Due to the short time of passage, there was no porosity formation in (bl).
(実施例2)
フラッシュ・スピニング法により得られたポリプロピレ
ンの三次元網状繊維の積層体を160℃の熱ロールにて
熱圧着し、最大孔径10μ、平均孔径5μ、ガーレ法通
気度5秒/ 100 cc、坪量s Og/rd、厚み
220μ、融点165°Cの不織布状物(a、)(旭化
成工業■製、ルクサーP■)を得た。(Example 2) A laminate of three-dimensional network fibers of polypropylene obtained by the flash spinning method was thermocompressed using a hot roll at 160°C, and the maximum pore diameter was 10μ, the average pore diameter was 5μ, and the Gurley method air permeability was 5 seconds/100. A non-woven fabric (a) (manufactured by Asahi Kasei Kogyo ■, Luxar P ■) having a thickness of 220 μm and a melting point of 165° C. was obtained.
分散液状となした融点90°Cのアイオノマー樹脂(c
、)(三井石油化学工業■製、ケミパール■)を、(c
2)上にロータリースクリーンを用いて5IIII11
間隔、巾2mmの斜線状に付与し、90°Cで乾燥した
後のアイオノマー樹脂の厚みは、1゜Oμである。Ionomer resin (c
) (manufactured by Mitsui Petrochemical Industries ■, Chemipearl ■), (c
2) 5III11 using rotary screen on top
The thickness of the ionomer resin after being applied in diagonal lines with a width of 2 mm and dried at 90°C is 1°Oμ.
次いで、エチレン−メタクリル酸共重合樹脂からなる融
点100℃、厚み20μ、孔径0. 3+mnφ、孔数
10ケ/ ctjのフィルム(bz) (三井石油化
学工業■製、ニュクレル■より作成)を(c2)上に重
ね、95゛cの熱風中を通過させ、(c2)の形状を保
持したまま(c2)と(c2)、(c2)と(b2)を
熱融着させた。Next, an ethylene-methacrylic acid copolymer resin having a melting point of 100°C, a thickness of 20μ, and a pore size of 0. A film (bz) with 3 + mnφ and 10 holes/ctj (manufactured by Mitsui Petrochemical Industries ■, made from Nucrel ■) was layered on top of (c2) and passed through hot air at 95°C to form the shape of (c2). While holding them, (c2) and (c2) and (c2) and (b2) were thermally fused.
(比較例2)
実施例2において、(c2)を使用せずに(c2)と(
b2)を重ね、105°cの熱風中を通過させ、(c2
)と(b2)を接着させた。(Comparative Example 2) In Example 2, (c2) and (
b2) and passed through hot air at 105°C, (c2
) and (b2) were adhered.
(実施例3)
ポリプロピレン系樹脂に炭酸カルシウムを混入し製膜後
、炭酸カルシウムを除いた融点160″C1最大孔径2
μ、平均孔径0.6μ、ガーレ法通気度120秒/ 1
00 cc、坪量63g10f、厚み140μの微多孔
膜(c3) (徳山曹達■製、NFシート 5140
■)に、低密度ポリエチレンを主体とした融点95°C
1直径400μの粒状樹脂(c3) (旭化成工業■
製、PAK 0025@)を10g10fで散布し、
次いで、ポリアミド樹脂を主体とした融点110℃、厚
み20μ、孔径O15rI1mφ、孔数4ケ/cT1の
フィルム(b、)を重ね、100°Cに熱せられた金属
ロールとゴムロール間に通過させ、(c3)の表面層の
みを融解し、(a、)と(c3)、(c3)と(bz)
を接着した。(Example 3) After forming a film by mixing calcium carbonate into polypropylene resin, the melting point excluding calcium carbonate was 160″C1, the maximum pore diameter was 2
μ, average pore diameter 0.6μ, Gurley method air permeability 120 seconds/1
00 cc, basis weight 63g10f, thickness 140μ microporous membrane (c3) (manufactured by Tokuyama Soda ■, NF sheet 5140
■) is mainly made of low density polyethylene with a melting point of 95°C.
1 400μ diameter granular resin (c3) (Asahi Kasei Kogyo ■
PAK 0025@) was sprayed at 10g10f,
Next, a film (b,) made mainly of polyamide resin with a melting point of 110°C, a thickness of 20μ, a pore diameter of O15rI1mφ, and a number of holes of 4/cT1 was layered and passed between a metal roll and a rubber roll heated to 100°C. Melting only the surface layer of c3), (a,) and (c3), (c3) and (bz)
was glued.
(比較例3)
実施例3において、(a、)と(bz)を重ね、105
°Cに熱せられた金属ロールとゴムロール間を通過させ
、(c3)と(bz)を接着させた。(Comparative Example 3) In Example 3, (a,) and (bz) were overlapped and 105
It was passed between a metal roll and a rubber roll heated to °C to bond (c3) and (bz) together.
以上の実施例及び比較例で得られた各包材のガーレ通気
度(秒/ 100 cc)を表にまとめて対比する。The Gurley air permeability (sec/100 cc) of each packaging material obtained in the above Examples and Comparative Examples is summarized in a table and compared.
なお、ガーレ法通気度は、JIS L1096Bに準
じて測定した。Note that the Gurley method air permeability was measured according to JIS L1096B.
(実施例4)
実施例1〜3により得られた通気性包材の(b)面を内
面にして、乾燥剤であるシリカゲル、脱臭剤である活性
炭、脱酸素剤である鉄粉をそれぞれ袋状となした各包材
に充填し、第3図に示す如く、三方のシールを行った。(Example 4) With the (b) side of the air-permeable packaging materials obtained in Examples 1 to 3 facing inside, silica gel as a desiccant, activated carbon as a deodorizer, and iron powder as an oxygen absorber were placed in bags. Each of the shaped packaging materials was filled and sealed on three sides as shown in FIG.
シール条件は、ヒートシールバーを使用し、130°C
で1秒間、他は140℃で1秒間、2.0kg/cdの
圧で行った。Sealing conditions are 130°C using a heat seal bar.
for 1 second at 140° C. and 1 second at 140° C. under a pressure of 2.0 kg/cd.
(c,)、(c2)、(c8)の何れも、それぞれ(b
、)、(b2)、(b、)中に埋没し、隙間なくヒート
シールされた。(c,), (c2), and (c8) are each (b
, ), (b2), and (b,), and were heat-sealed without any gaps.
本発明による通気性包体(実施例)は、従来の方法によ
り得られた包体(比較例)に比較して、速やかな脱湿、
脱臭、脱酸素などが行われ有用であった。The breathable packaging according to the present invention (Example) has faster dehumidification,
It was useful for deodorizing and deoxidizing.
(発明の効果)
本発明においては、微多孔膜もしくは不織布状物(a)
と通気性有孔合成樹脂製フィルム(b)の間に、部分的
に位置させたホットメルト性合成樹脂(c)を介在させ
た構造の包材とすることにより、この(c)部分を存在
させない従来法の包材に比較して、より通気性を向上さ
せることができる。(Effect of the invention) In the present invention, microporous membrane or nonwoven fabric (a)
By using a packaging material with a structure in which a partially positioned hot-melt synthetic resin (c) is interposed between a permeable perforated synthetic resin film (b), this part (c) is Compared to conventional packaging materials that do not allow air permeability, air permeability can be further improved.
第1−1図は、本発明の構成の通気性包材の横断面図で
ある。
第1−2図は、本発明の構成の通気性包材の平面図であ
る。
第2〜3図は、本発明の構成の通気性包材を一部又は全
部用いて作られた通気性包体を示す横断面図である。
第4−1図は、従来法の構成の通気性包材の横断面図で
ある。
第4−2図は、従来法の構成の通気性包材の平面図であ
る。
a:微多孔膜または不織布状物(a)、b:孔部1を有
する通気性の有孔合成樹脂製フィルム(b)、
C:(b)より融点が低い合成樹脂(c)、d:他案材
フィルム、
1:孔部、
2:ヒートシール部、
□□−一」FIG. 1-1 is a cross-sectional view of a breathable packaging material constructed according to the present invention. 1-2 is a plan view of a breathable packaging material constructed according to the present invention. FIGS. 2 and 3 are cross-sectional views showing a breathable packaging made using a part or all of the breathable packaging material according to the present invention. FIG. 4-1 is a cross-sectional view of a breathable packaging material constructed according to a conventional method. FIG. 4-2 is a plan view of an air-permeable packaging material constructed according to a conventional method. a: Microporous membrane or non-woven fabric (a), b: Breathable perforated synthetic resin film having 1 hole (b), C: synthetic resin with a lower melting point than (b) (c), d: Other material film, 1: Hole part, 2: Heat seal part, □□-1"
Claims (5)
1〜10,000秒/100ccである微多孔膜もしく
は不織布状物と、 (b)、(a)より融点が低く、通気性を有する有孔の
合成樹脂製フィルムとの間に、 (c)、(b)より融点が低い合成樹脂を部分的に位置
せしめ、(a)と(c)、(c)と(b)を接着してな
る(a)、(b)、(c)の一体の通気性包材。(1) (a) The pore diameter is 50μ or less and the Gurley method air permeability is 0.
1 to 10,000 seconds/100cc between a microporous membrane or nonwoven material and a perforated synthetic resin film having a lower melting point than (b) and (a) and having air permeability, (c) , a synthetic resin with a lower melting point than that of (b) is partially placed, and (a) and (c), and (c) and (b) are bonded together to form a unitary structure of (a), (b), and (c). Breathable packaging material.
使用し、(a)面を外面として内部に固体を包含させ、
周囲を熱融着し、当該固体が漏洩しないようになした通
気性包体。(2) Using all or part of the breathable packaging material according to claim (1), with the (a) side as the outer surface and a solid contained therein;
A breathable envelope whose surroundings are heat-sealed to prevent the solid from leaking.
(a)が、炭酸カルシウム、微細フィラー等の無機質材
をブレンドしてなるポリエチレン、ポリプロピレン等の
ポリオレフィン系樹脂フィルムから該無機質材の除去に
より得られる微多孔膜、またはフラッシュ・スピニング
法により得られたポリオレフィン系繊維の積層物である
、請求項(1)記載の通気性包材及び請求項(2)記載
の包体。(3) The microporous membrane or nonwoven fabric (a) according to claim (1) is made of a polyolefin resin film such as polyethylene or polypropylene blended with an inorganic material such as calcium carbonate or a fine filler. The breathable packaging material according to claim (1) and the packaging according to claim (2), which are a microporous membrane obtained by removal or a laminate of polyolefin fibers obtained by flash spinning.
合成樹脂(c)が、ポリエチレン、エチレン−酢酸ビニ
ル系共重合樹脂、エチレン−アクリレート系共重合樹脂
、エチレン−メタクリル酸系共重合樹脂、アイオノマー
樹脂、ポリアミド樹脂及びこれらの変性樹脂または前記
樹脂の2種以上の混合物からなる群から選ばれた材料で
ある、請求項(1)記載の通気性包材及び請求項(2)
記載の包体。(4) the synthetic resin film (b) according to claim (1);
The synthetic resin (c) is polyethylene, ethylene-vinyl acetate copolymer resin, ethylene-acrylate copolymer resin, ethylene-methacrylic acid copolymer resin, ionomer resin, polyamide resin, modified resins thereof, or two of the above resins. The breathable packaging material according to claim (1) and claim (2), which are made of a material selected from the group consisting of a mixture of more than one species.
Encapsulation as described.
又は(a)面に平行な線状又は格子状に位置している、
請求項(1)記載の通気性包材及び請求項(2)記載の
包体。(5) The synthetic resin (c) according to claim (1) is dotted,
or (a) located in a line or grid pattern parallel to the plane;
The breathable packaging material according to claim (1) and the packaging according to claim (2).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13411990A JPH0429840A (en) | 1990-05-25 | 1990-05-25 | Gas permeable packaging material and packaged body therewith |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13411990A JPH0429840A (en) | 1990-05-25 | 1990-05-25 | Gas permeable packaging material and packaged body therewith |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0429840A true JPH0429840A (en) | 1992-01-31 |
Family
ID=15120908
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13411990A Pending JPH0429840A (en) | 1990-05-25 | 1990-05-25 | Gas permeable packaging material and packaged body therewith |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0429840A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05220880A (en) * | 1992-02-08 | 1993-08-31 | Nidaiki Kk | Plastic composite material |
JPH08230114A (en) * | 1995-03-01 | 1996-09-10 | Kawasaki Steel Corp | Paper machine-made stampable sheet, lightweight stampable sheet molding and lightweight stampable sheet skin-laminated product |
JPH0976390A (en) * | 1995-09-13 | 1997-03-25 | Tokuyama Corp | Laminated film |
JPH10323955A (en) * | 1997-05-27 | 1998-12-08 | Toppan Printing Co Ltd | Sterilizing blister packaging mount and blister package |
JPH11100766A (en) * | 1997-09-22 | 1999-04-13 | Masao Ueda | Air-permeable bag cloth, and its production |
US6306352B1 (en) * | 1997-09-26 | 2001-10-23 | Mitsubishi Gas Chemical Company, Inc. | Oxygen generating materials, carbon dioxide absorbing materials, and transport system and transport method of live fishery products |
JP2002144451A (en) * | 2000-11-09 | 2002-05-21 | Nippon Petrochem Co Ltd | Method for producing package using packaging material reinforced with net-shaped reinforced layer and package made of the packaging material |
JP2008222307A (en) * | 2007-03-08 | 2008-09-25 | Bosung Industry Co Ltd | Breathing container of scent and its manufacturing method |
JP2017058185A (en) * | 2015-09-15 | 2017-03-23 | 大和製衡株式会社 | Weighing apparatus |
JP2018070179A (en) * | 2016-10-25 | 2018-05-10 | 株式会社ニトムズ | Bag-body constituting member, bag body, and throwaway body warmer |
US11509123B2 (en) | 2016-07-25 | 2022-11-22 | Osaka University | Wiring sheet, sheet-shaped system, and structure operation support system |
-
1990
- 1990-05-25 JP JP13411990A patent/JPH0429840A/en active Pending
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05220880A (en) * | 1992-02-08 | 1993-08-31 | Nidaiki Kk | Plastic composite material |
JPH08230114A (en) * | 1995-03-01 | 1996-09-10 | Kawasaki Steel Corp | Paper machine-made stampable sheet, lightweight stampable sheet molding and lightweight stampable sheet skin-laminated product |
JPH0976390A (en) * | 1995-09-13 | 1997-03-25 | Tokuyama Corp | Laminated film |
JPH10323955A (en) * | 1997-05-27 | 1998-12-08 | Toppan Printing Co Ltd | Sterilizing blister packaging mount and blister package |
JPH11100766A (en) * | 1997-09-22 | 1999-04-13 | Masao Ueda | Air-permeable bag cloth, and its production |
US6306352B1 (en) * | 1997-09-26 | 2001-10-23 | Mitsubishi Gas Chemical Company, Inc. | Oxygen generating materials, carbon dioxide absorbing materials, and transport system and transport method of live fishery products |
US6612259B2 (en) | 1997-09-26 | 2003-09-02 | Mitsubishi Gas Chemical Company, Inc. | Oxygen generating materials, carbon dioxide absorbing materials, and transport system and transport method of live fishery products |
JP2002144451A (en) * | 2000-11-09 | 2002-05-21 | Nippon Petrochem Co Ltd | Method for producing package using packaging material reinforced with net-shaped reinforced layer and package made of the packaging material |
JP2008222307A (en) * | 2007-03-08 | 2008-09-25 | Bosung Industry Co Ltd | Breathing container of scent and its manufacturing method |
JP2017058185A (en) * | 2015-09-15 | 2017-03-23 | 大和製衡株式会社 | Weighing apparatus |
US11509123B2 (en) | 2016-07-25 | 2022-11-22 | Osaka University | Wiring sheet, sheet-shaped system, and structure operation support system |
JP2018070179A (en) * | 2016-10-25 | 2018-05-10 | 株式会社ニトムズ | Bag-body constituting member, bag body, and throwaway body warmer |
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