JP2015093414A - Air-permeable laminate, and disposable body warmer obtained by using the same - Google Patents
Air-permeable laminate, and disposable body warmer obtained by using the same Download PDFInfo
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- JP2015093414A JP2015093414A JP2013233432A JP2013233432A JP2015093414A JP 2015093414 A JP2015093414 A JP 2015093414A JP 2013233432 A JP2013233432 A JP 2013233432A JP 2013233432 A JP2013233432 A JP 2013233432A JP 2015093414 A JP2015093414 A JP 2015093414A
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- porous film
- nonwoven fabric
- density polyethylene
- breathable
- breathable laminate
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- 230000035699 permeability Effects 0.000 claims abstract description 60
- 239000004745 nonwoven fabric Substances 0.000 claims abstract description 58
- 238000000034 method Methods 0.000 claims abstract description 47
- 239000011148 porous material Substances 0.000 claims abstract description 32
- 239000011256 inorganic filler Substances 0.000 claims abstract description 28
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 28
- 239000000835 fiber Substances 0.000 claims abstract description 26
- 229920001684 low density polyethylene Polymers 0.000 claims abstract description 19
- 239000004702 low-density polyethylene Substances 0.000 claims abstract description 19
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052753 mercury Inorganic materials 0.000 claims abstract description 10
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 10
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 10
- 239000000470 constituent Substances 0.000 claims abstract description 8
- 239000000853 adhesive Substances 0.000 claims description 32
- 230000001070 adhesive effect Effects 0.000 claims description 29
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical group [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 22
- 229920000092 linear low density polyethylene Polymers 0.000 claims description 21
- 239000004707 linear low-density polyethylene Substances 0.000 claims description 21
- 229920005989 resin Polymers 0.000 claims description 17
- 239000011347 resin Substances 0.000 claims description 17
- 238000004898 kneading Methods 0.000 claims description 16
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 11
- 229920000728 polyester Polymers 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 7
- 229920002647 polyamide Polymers 0.000 claims description 7
- 239000004952 Polyamide Substances 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 229920000098 polyolefin Polymers 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000002074 melt spinning Methods 0.000 claims description 2
- 229920005992 thermoplastic resin Polymers 0.000 claims description 2
- 238000005304 joining Methods 0.000 claims 3
- 230000035515 penetration Effects 0.000 abstract 1
- -1 polyethylene terephthalate Polymers 0.000 description 11
- 238000007789 sealing Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 239000002994 raw material Substances 0.000 description 10
- 230000020169 heat generation Effects 0.000 description 9
- 238000010030 laminating Methods 0.000 description 9
- 229920001225 polyester resin Polymers 0.000 description 9
- 239000004645 polyester resin Substances 0.000 description 9
- 239000003963 antioxidant agent Substances 0.000 description 8
- 230000003078 antioxidant effect Effects 0.000 description 8
- 238000009826 distribution Methods 0.000 description 8
- 239000012968 metallocene catalyst Substances 0.000 description 8
- 230000008569 process Effects 0.000 description 8
- 239000004698 Polyethylene Substances 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- 229920000573 polyethylene Polymers 0.000 description 7
- 235000021355 Stearic acid Nutrition 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 6
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 6
- 239000008117 stearic acid Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000004831 Hot glue Substances 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000011800 void material Substances 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000004049 embossing Methods 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 229920006225 ethylene-methyl acrylate Polymers 0.000 description 2
- 239000012943 hotmelt Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920013716 polyethylene resin Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- 239000010455 vermiculite Substances 0.000 description 2
- 229910052902 vermiculite Inorganic materials 0.000 description 2
- 235000019354 vermiculite Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910001868 water Inorganic materials 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- IVORCBKUUYGUOL-UHFFFAOYSA-N 1-ethynyl-2,4-dimethoxybenzene Chemical compound COC1=CC=C(C#C)C(OC)=C1 IVORCBKUUYGUOL-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 206010016322 Feeling abnormal Diseases 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical class [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- BKMNYKYGRHOVEO-UHFFFAOYSA-N [O-2].[Mg+2].O.[Ni]=O Chemical compound [O-2].[Mg+2].O.[Ni]=O BKMNYKYGRHOVEO-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- HHSPVTKDOHQBKF-UHFFFAOYSA-J calcium;magnesium;dicarbonate Chemical compound [Mg+2].[Ca+2].[O-]C([O-])=O.[O-]C([O-])=O HHSPVTKDOHQBKF-UHFFFAOYSA-J 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000010227 cup method (microbiological evaluation) Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009820 dry lamination Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 125000005670 ethenylalkyl group Chemical group 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- OJNCHCKDZDXZKT-UHFFFAOYSA-N magnesium zinc oxygen(2-) hydrate Chemical compound [Mg+2].O.[O-2].[Zn+2].[O-2] OJNCHCKDZDXZKT-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229920001526 metallocene linear low density polyethylene Polymers 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000002459 porosimetry Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 229920006345 thermoplastic polyamide Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
本発明は通気性積層体及びそれを用いた使い捨てカイロに関する。より詳細には、構成成分が良く混練分散された多孔質フィルムを用いることにより、微細孔の分布が均等化され、通気性および透湿性がコントロールされた通気性積層体及びそれを用いた使い捨てカイロに関する。 The present invention relates to a breathable laminate and a disposable body warmer using the same. More specifically, by using a porous film in which the constituent components are well kneaded and dispersed, the breathable laminate in which the distribution of fine pores is made uniform and the breathability and moisture permeability are controlled, and the disposable body warmer using the same About.
現在、カイロ(使い捨てカイロ等)の発熱体を封入する収容袋(袋体)を構成する部材(袋体構成部材)としては、多孔質フィルムと不織布などの通気性基材とを接着してなる通気性の材料(通気材)が知られている。例えば、下記特許文献1には、1軸延伸した多孔質フィルムの片面に補強材が積層された通気性且つ透湿性の積層体が開示され、下記特許文献2には、融点に差のあるA層およびB層の2層の多孔質フィルムからなる袋体構成部材が開示され、下記特許文献3には、不織布と多孔質フィルムとを接着する際の接着剤の塗布量を変えることで通気性の均一化を図ったカイロ用積層体が開示され、下記特許文献4には、多孔質フィルムにポリエステル不織布が積層された通気材からなり、変形しにくく、使用時に違和感のないカイロ用通気材が開示されている。 At present, as a member (bag body constituting member) constituting a storage bag (bag body) enclosing a heating element of a warmer (disposable body warmer, etc.), a porous film and a breathable base material such as a nonwoven fabric are bonded. Breathable materials (breathing materials) are known. For example, the following Patent Document 1 discloses a breathable and moisture-permeable laminate in which a reinforcing material is laminated on one side of a uniaxially stretched porous film, and the following Patent Document 2 discloses an A having a difference in melting point. A bag-constituting member composed of a two-layer porous film consisting of a layer B and a B-layer is disclosed, and the following Patent Document 3 discloses breathability by changing the amount of adhesive applied when bonding a nonwoven fabric and a porous film. A layered body for warmers is disclosed, and the following patent document 4 is made of a breathable material in which a polyester non-woven fabric is laminated on a porous film, and is not easily deformed and does not feel strange when used. It is disclosed.
これらのカイロには、微細な通気孔を有する多孔質フィルムの開孔分布が均等化され、発熱した時の最高温度及び発熱の持続時間などの使い捨てカイロの特性に問題のない袋体が必要とされている。 These warmers require a bag that has a uniform distribution of pores in a porous film having fine ventilation holes and that has no problems with the characteristics of disposable warmers such as the maximum temperature when heat is generated and the duration of heat generation. Has been.
本発明の目的は、使い捨てカイロの袋体構成部材に使用した際に、熱シール性が良く、発熱最高温度および発熱持続時間などの使い捨てカイロの製品特性に優れ、且つ熱シール時のエッジ切れなどが少なく生産性に優れた、不織布と多孔質フィルムとの通気性積層体を提供することである。 The object of the present invention is that when used for a bag component of a disposable body warmer, the heat sealability is good, the product characteristics of the disposable body warmer such as the maximum heat generation temperature and the heat generation duration are excellent, and the edge breaks during heat sealing, etc. It is an object to provide a breathable laminate of a nonwoven fabric and a porous film that has little productivity and excellent productivity.
本発明者らは、鋭意検討した結果、密度および粘性の異なる樹脂を配合すること、および特定の混錬機で樹脂を混錬・溶融することで、製膜加工性が良好となり、延伸ムラを少なく、孔の分散性を向上させることができ、その結果、特定の細孔径および細孔体積を有する、幅および長さ方向の通気性のバラツキが小さく、熱シール性に優れた多孔質フィルムが得られ、この多孔質フィルムを用いることによって上記目的が達成されることを見出だし、本発明を完成させたものである。 As a result of intensive investigations, the inventors have found that film forming workability is improved by blending resins with different densities and viscosities, and kneading and melting the resin with a specific kneading machine, and stretching unevenness. Therefore, a porous film having a specific pore diameter and pore volume, small variation in air permeability in the width and length directions, and excellent heat sealability can be obtained. It was found that the above object was achieved by using this porous film, and the present invention was completed.
すなわち、本発明は以下のとおりである。
(1)不織布と多孔質フィルムとが接合されている通気性積層体であって、該不織布は部分熱圧着率が5〜25%および目付けが15〜50g/m2可塑性長繊維不織布からなり、該多孔質フィルムは、構成成分として直鎖状低密度ポリエチレンを40〜62wt%、低密度ポリエチレンを2〜10wt%および無機充填剤を35〜50wt%含有し、坪量が40〜100g/m2、水銀圧入法によるメディアン径および細孔体積がそれぞれ1μm以下および0.3ml/g以上、並びに10%伸長時の応力が5N/10mm以上の多孔質フィルムであり、王研式透気度が5000〜100000秒/100ccであることを特徴とする通気性積層体。
(2)前記無機充填剤が、50%平均粒径が1〜10μmの炭酸カルシュウムであることを特徴とする前記(1)に記載の通気性積層体。
(3)前記熱可塑性長繊維不織布がポリエステル系繊維、ポリアミド系繊維およびポリオレフィン系繊維から選ばれた少なくとも1種からなることを特徴とする前記(1)または(2)に記載の通気性積層体。
(4)前記多孔質フィルムが、延伸倍率が3〜5倍であることを特徴とする前記(1)〜(3)のいずれか一項に記載の通気性積層体。
(5)前記接合は部分的接合であって、非接合面積率が15〜55%であることを特徴とする前記(1)〜(4)のいずれか一項に記載の通気性積層体。
(6)前記(1)〜(5)のいずれか一項に記載の通気性積層体を袋体構成部材として用いた使い捨てカイロ。
(7)スパンボンド法で熱可塑性樹脂を溶融紡糸して得られた目付15〜50g/m2の部分熱圧着された熱可塑性長繊維不織布と、構成成分として直鎖状低密度ポリエチレンを40〜62wt%、低密度ポリエチレンを2〜10wt%および無機充填剤を35〜50wt%含有する混合樹脂を2軸混練押出機で混合分散させた後、ギヤポンプ付き2軸混錬押出機にて、Tダイ法を用いて溶融成膜した未延伸フィルムを、延伸温度40〜100℃で1軸に3〜5倍延伸し、次いで5〜20%緩和で熱セットして得られた坪量40〜100g/m2の多孔質フィルムとを、接着剤を用い、非接合面積率が15〜55%となるように部分的に接合することを特徴とする通気性積層体の製造方法。
That is, the present invention is as follows.
(1) A breathable laminate in which a nonwoven fabric and a porous film are joined, wherein the nonwoven fabric comprises a partial thermocompression bonding rate of 5 to 25% and a basis weight of 15 to 50 g / m 2 plastic long fiber nonwoven fabric, The porous film contains 40 to 62 wt% of linear low density polyethylene, 2 to 10 wt% of low density polyethylene and 35 to 50 wt% of inorganic filler as constituent components, and has a basis weight of 40 to 100 g / m 2. A porous film having a median diameter and pore volume of 1 μm or less and 0.3 ml / g or more by mercury intrusion method, and a stress at 10% elongation of 5 N / 10 mm or more, respectively. Breathable laminate characterized by ˜100,000 seconds / 100 cc.
(2) The breathable laminate according to (1), wherein the inorganic filler is calcium carbonate having a 50% average particle diameter of 1 to 10 μm.
(3) The breathable laminate according to (1) or (2), wherein the thermoplastic long-fiber nonwoven fabric comprises at least one selected from polyester fibers, polyamide fibers, and polyolefin fibers. .
(4) The breathable laminate according to any one of (1) to (3), wherein the porous film has a draw ratio of 3 to 5 times.
(5) The breathable laminate according to any one of (1) to (4), wherein the bonding is partial bonding, and a non-bonding area ratio is 15 to 55%.
(6) A disposable body warmer using the breathable laminated body according to any one of (1) to (5) as a bag constituting member.
(7) Partially thermocompression-bonded thermoplastic long-fiber nonwoven fabric having a basis weight of 15 to 50 g / m 2 obtained by melt spinning a thermoplastic resin by a spunbond method, and 40 to 40 of linear low-density polyethylene as a constituent component A mixed resin containing 62 wt%, low density polyethylene 2 to 10 wt% and inorganic filler 35 to 50 wt% was mixed and dispersed by a twin screw kneading extruder, and then a T die was added by a twin screw kneading extruder with a gear pump. An unstretched film melt-formed using a method is stretched 3 to 5 times uniaxially at a stretching temperature of 40 to 100 ° C., and then heat-set with 5 to 20% relaxation to obtain a basis weight of 40 to 100 g / A method for producing a breathable laminate, comprising: bonding an m 2 porous film partially using an adhesive so that a non-bonded area ratio is 15 to 55%.
特定の不織布と特定の多孔質フィルムが部分的に接合された本発明の通気性積層体は、袋形状にして、発熱組成物を入れ、貼るカイロに用いた場合、発熱最高温度および発熱持続時間などの調整が良好にでき、使い捨てカイロ包装材などとして好ましく用いることができる。
また、直鎖状低密度ポリエチレン、低密度ポリエチレンおよび無機充填材を含有する混合樹脂を特定の混錬機で混錬・溶融することにより、無機充填材の分散性を向上させることができ、且つ、延伸加工時の延伸ムラも少なく、微細な孔が生じ、細孔体積が大きくでき、好適なヒートシール性が得られ、熱シール時のエッジ切れを少なくできるなどの効果が得られる。
さらに、多孔質フィルム成型時の延伸倍率を3〜5倍に調整することにより、熱シール時のエッジ切れを少なくできる。
The breathable laminate of the present invention, in which a specific nonwoven fabric and a specific porous film are partially bonded, is formed into a bag shape, puts a heat generating composition, and is used as a paste warmer. Etc., and can be preferably used as a disposable warmer packaging material.
Moreover, the dispersibility of the inorganic filler can be improved by kneading and melting the mixed resin containing linear low density polyethylene, low density polyethylene and the inorganic filler with a specific kneading machine, and Further, there is little stretching unevenness at the time of stretching processing, fine pores are generated, the pore volume can be increased, suitable heat sealability can be obtained, and edge breakage at the time of heat sealing can be reduced.
Furthermore, the edge breakage at the time of heat sealing can be reduced by adjusting the stretch ratio at the time of molding the porous film to 3 to 5 times.
本発明の通気性積層体は特定の熱可塑性長繊維不織布と特定の多孔質フィルムとが接合されているものである。本発明の通気性積層体を使い捨てカイロに用いた場合、該多孔質フィルムは、使い捨てカイロの発熱に必要な通気性および透湿性を調整できる微細孔を有している。また、該長繊維不織布は、該多孔質フィルムの保護および補強、並びに製袋加工性の改良などの目的で使用されている。 The breathable laminate of the present invention is obtained by bonding a specific thermoplastic long-fiber nonwoven fabric and a specific porous film. When the air-permeable laminate of the present invention is used in a disposable body warmer, the porous film has fine holes that can adjust the air permeability and moisture permeability necessary for heat generation of the disposable body warmer. Further, the long fiber nonwoven fabric is used for the purpose of protecting and reinforcing the porous film and improving bag-making processability.
本発明に用いる熱可塑性長繊維不織布は、特に限定されないが、比較的薄く、強力および耐摩耗性に優れた、スパンボンド法の長繊維不織布が好ましい。不織布を構成する繊維としては、例えば、ナイロン6、ナイロン66および共重合ポリアミドなどのポリアミド系繊維、ポリエチレンテレフタレート(PET)、ポリブチレンテレフタレート(PBT)および共重合ポリエステルなどのポリエステル系繊維、並びにポリエチレンおよびポリプロピレンなどのポリオレフィン系繊維を用いることができる。また、芯にポリエチレンテレフタレート、鞘にポリエチレンを用いた芯鞘構造などの複合繊維を用いてもよい。 The thermoplastic long-fiber nonwoven fabric used in the present invention is not particularly limited, but a spunbonded long-fiber nonwoven fabric that is relatively thin and excellent in strength and abrasion resistance is preferable. Examples of the fibers constituting the nonwoven fabric include polyamide fibers such as nylon 6, nylon 66 and copolymer polyamide, polyester fibers such as polyethylene terephthalate (PET), polybutylene terephthalate (PBT) and copolymer polyester, polyethylene and Polyolefin fibers such as polypropylene can be used. Alternatively, a composite fiber such as a core-sheath structure using polyethylene terephthalate for the core and polyethylene for the sheath may be used.
本発明に用いる長繊維不織布は、スパンボンド法で製造された不織布が好ましく、部分熱圧着率(エンボス面積率)が5〜25%、好ましくは7〜20%であり、目付が15〜50g/m2、好ましくは20〜40g/m2である。部分熱圧着率が5%未満または目付が15g/m2未満では、強度および耐摩耗強度が低下する、一方、部分熱圧着率が25%を超えるか、または目付が50g/m2を超えると、強度および耐摩耗性は高くなるが、硬い風合いとなるなどの問題がある。 The long-fiber nonwoven fabric used in the present invention is preferably a nonwoven fabric produced by a spunbond method, has a partial thermocompression bonding ratio (embossed area ratio) of 5 to 25%, preferably 7 to 20%, and a basis weight of 15 to 50 g / m 2 , preferably 20 to 40 g / m 2 . When the partial thermocompression bonding rate is less than 5% or the basis weight is less than 15 g / m 2 , the strength and the wear resistance are lowered. On the other hand, when the partial thermocompression bonding rate exceeds 25% or the basis weight exceeds 50 g / m 2. Strength and wear resistance are increased, but there are problems such as a hard texture.
さらに、上記不織布は、エンボス加工が施されたスパンボンド不織布であり、特に、熱エンボスロールによるエンボス加工が施されたスパンボンド不織布であることが好ましい。上記のエンボス加工におけるエンボスの形状は、特に限定されず、例えば長方形や円形などが挙げられる。また、エンボス1個当たりの面積は、特に限定されないが、0.1〜10mm2が好ましく、より好ましくは0.3〜5mm2である。上記面積が0.1mm2未満では、面積が小さすぎて熱融着による強度が得られないため、また10mm2を超えると、エンボス1つ1つの間隔が大きくなるため、耐摩耗強度が低下する。 Furthermore, the nonwoven fabric is a spunbond nonwoven fabric that has been embossed, and is particularly preferably a spunbond nonwoven fabric that has been embossed by a hot embossing roll. The shape of the embossing in the above embossing is not particularly limited, and examples thereof include a rectangle and a circle. Moreover, although the area per emboss is not specifically limited, 0.1-10 mm < 2 > is preferable, More preferably, it is 0.3-5 mm < 2 >. If the area is less than 0.1 mm 2 , the area is too small to obtain the strength by heat fusion, and if it exceeds 10 mm 2 , the distance between each emboss increases, so the wear resistance decreases. .
本発明の通気性積層体における多孔質フィルムは、直鎖状低密度ポリエチレン、低密度ポリエチレンおよび無機充填剤の混合物から構成されることが好ましい。このような構成の多孔質フィルムは、中間モジュラスが向上でき、未延伸フィルムの延伸加工を行うことで多孔質化でき、且つ延伸ムラが減少できるなどの特長を有している。 The porous film in the breathable laminate of the present invention is preferably composed of a mixture of linear low density polyethylene, low density polyethylene and an inorganic filler. The porous film having such a configuration has the advantages that the intermediate modulus can be improved, the porous film can be made porous by stretching the unstretched film, and stretching unevenness can be reduced.
直鎖状低密度ポリエチレンは、エチレンと炭素数が4〜8のα−オレフィンモノマーとを重合して得られる直鎖状ポリエチレンである。上記直鎖状低密度ポリエチレンに用いられるα−オレフィンモノマーとしては、1−ブテン、1−オクテン、1−ヘキセン、4−メチルペンテン−1が好ましい。上記直鎖状低密度ポリエチレンにおいて、全構成モノマーの繰り返し単位(全ての構成モノマーに起因する繰り返し単位)に対するエチレンモノマーの繰り返し単位(エチレンモノマーに起因する繰り返し単位)の含有量(含有率)は90モル%以上が好ましい。
上記直鎖状低密度ポリエチレンとしては、中でも、より低温におけるヒートシール性向上の観点から、メタロセン系触媒を用いて調製された、いわゆる、メタロセン系直鎖状低密度ポリエチレン(メタロセン系LLDPE)が特に好ましい。
The linear low density polyethylene is a linear polyethylene obtained by polymerizing ethylene and an α-olefin monomer having 4 to 8 carbon atoms. As the α-olefin monomer used in the linear low density polyethylene, 1-butene, 1-octene, 1-hexene and 4-methylpentene-1 are preferable. In the above-mentioned linear low density polyethylene, the content (content ratio) of the ethylene monomer repeating unit (repeating unit derived from ethylene monomer) with respect to the repeating unit of all constituting monomers (repeating unit derived from all constituent monomers) is 90. More than mol% is preferable.
As the linear low-density polyethylene, from the viewpoint of improving heat-sealability at a lower temperature, a so-called metallocene linear low-density polyethylene (metallocene LLDPE) prepared using a metallocene catalyst is particularly used. preferable.
メタロセン触媒の直鎖状低密度ポリエチレンは、密度が0.90〜0.94g/cm3、190℃におけるMFRが1〜15g/10分、融点が101〜125℃の範囲内であることが好ましい。また、密度違いの2種以上を混合することが好ましく、例えば、低密度および低融点の直鎖状低密度ポリエチレンを配合することで、溶液粘度が調整でき、押し出し成形加工性及び製袋加工時のヒートシール性などを向上させることができる。 The metallocene catalyst linear low density polyethylene preferably has a density of 0.90 to 0.94 g / cm 3 , an MFR at 190 ° C. of 1 to 15 g / 10 min, and a melting point of 101 to 125 ° C. . Moreover, it is preferable to mix two or more types having different densities. For example, by blending a low-density and low-melting linear low-density polyethylene, the solution viscosity can be adjusted, and the extrusion processability and the bag making process can be adjusted. It is possible to improve the heat sealability.
前記低密度ポリエチレン、即ち高圧法の低密度ポリエチレンの密度は、0.900〜0.930g/cm3が好ましく、より好ましくは0.910〜0.925g/cm3である。また、高圧法低密度ポリエチレンの190℃におけるMFRは、特に限定されないが、1.0〜3.0g/10分が好ましく、より好ましくは1.5〜2.5g/10分である。
なお、本発明における密度とはJIS K 6922−2及びJIS K 7112に準拠して得られた密度をいうものとする。また、本発明におけるMFRはISO1133(JIS K 7210)に準拠して測定することができる。
The density of the low density polyethylene, that is, the low density polyethylene of the high pressure method is preferably 0.900 to 0.930 g / cm 3 , more preferably 0.910 to 0.925 g / cm 3 . Moreover, although MFR in 190 degreeC of a high pressure method low density polyethylene is not specifically limited, 1.0-3.0 g / 10min is preferable, More preferably, it is 1.5-2.5 g / 10min.
In addition, the density in this invention shall mean the density obtained based on JISK6922-2 and JISK7112. Moreover, MFR in this invention can be measured based on ISO1133 (JISK7210).
本発明に用いられる多孔質フィルムは無機充填剤を含有することが好ましい。該無機充填剤は、延伸により充填剤の周囲にボイド(孔)を発生させることによって、フィルムを多孔質化させる役割を担う。かかる無機充填剤としては、例えば、タルク、シリカ、石粉、ゼオライト、アルミナ、アルミニウム粉末および鉄粉の他、炭酸カルシウム、炭酸マグネシウム、炭酸マグネシウム−カルシウムおよび炭酸バリウム等の炭酸の金属塩、硫酸マグネシウムおよび硫酸バリウム等の硫酸の金属塩、酸化亜鉛、酸化チタンおよび酸化マグネシウム等の金属酸化物、水酸化アルミニウム、水酸化マグネシウム、水酸化ジルコニウム、水酸化カルシウムおよび水酸化バリウム等の金属水酸化物、並びに酸化マグネシウム−酸化ニッケルの水和物および酸化マグネシウム−酸化亜鉛の水和物等の金属水和物(水和金属化合物)などが挙げられる。中でも、炭酸カルシウムおよび硫酸バリウムが好ましい。無機充填剤の形状は、延伸によるボイド(孔)形成の観点から、粒子状が好ましい。即ち、無機充填剤としては炭酸カルシウムからなる無機粒子が好ましい。無機充填剤は飽和脂肪酸処理されたものが好ましく用いられる。 The porous film used in the present invention preferably contains an inorganic filler. The inorganic filler plays a role of making the film porous by generating voids (pores) around the filler by stretching. Examples of such inorganic fillers include talc, silica, stone powder, zeolite, alumina, aluminum powder and iron powder, as well as metal carbonates of carbonates such as calcium carbonate, magnesium carbonate, magnesium carbonate-calcium and barium carbonate, magnesium sulfate and Metal salts of sulfuric acid such as barium sulfate, metal oxides such as zinc oxide, titanium oxide and magnesium oxide, metal hydroxides such as aluminum hydroxide, magnesium hydroxide, zirconium hydroxide, calcium hydroxide and barium hydroxide, and Examples thereof include metal hydrates (hydrated metal compounds) such as magnesium oxide-nickel oxide hydrate and magnesium oxide-zinc oxide hydrate. Of these, calcium carbonate and barium sulfate are preferred. The shape of the inorganic filler is preferably particulate from the viewpoint of forming voids (pores) by stretching. That is, as the inorganic filler, inorganic particles made of calcium carbonate are preferable. As the inorganic filler, those treated with a saturated fatty acid are preferably used.
無機充填剤の粒径としては、粒度分布測定における50%平均粒径(D=50%)で1.0〜10μmが好ましく、さらに好ましくは、2.0〜7.0μm、特に好ましくは2.5〜5.0μmである。粒径がこの範囲にあると、延伸加工でボイド形成性が向上し、フィルムの破れおよび外観不良などが抑制される。粒径が1μm未満では、分散不良が起こりやすく、凝集しやすくなる。一方、10μmを越えると、樹脂に対する添加量を多くできるが、延伸加工時に開孔径が大きくなり、通気性が高くなり、透湿度が低下し、且つ、延伸加工時の無機充填剤の脱落が多くなり、貫通孔が生じやすくなる。 The particle size of the inorganic filler is preferably 1.0 to 10 μm, more preferably 2.0 to 7.0 μm, and particularly preferably 2.50% average particle size (D = 50%) in particle size distribution measurement. 5 to 5.0 μm. When the particle size is in this range, the void-forming property is improved by stretching, and film breakage and poor appearance are suppressed. If the particle size is less than 1 μm, poor dispersion tends to occur and aggregation tends to occur. On the other hand, if it exceeds 10 μm, the amount added to the resin can be increased, but the pore diameter is increased during stretching, the air permeability is increased, the moisture permeability is decreased, and the inorganic filler is largely removed during stretching. It becomes easy to produce a through-hole.
前記無機充填剤の含有量は、フィルム全重量に対して35〜50wt%が好ましく、さらに好ましくは37〜48wt%、特に好ましくは40〜47wt%である。含有量がこの範囲であると、延伸加工時のボイド加工性が良好になり、且つ製膜時の破れおよび外観不良が抑制される。無機充填剤が35%未満ではボイド形成性が低下する。一方、50wt%を越えると、ボイド形成性は良くなるが、透気度が過剰になり、且つ、延伸加工時に無機充填剤の脱落、ピンホール、破れおよび外観不良が生じやすくなる。 The content of the inorganic filler is preferably 35 to 50 wt%, more preferably 37 to 48 wt%, particularly preferably 40 to 47 wt% with respect to the total weight of the film. When the content is within this range, the void processability during stretching is good, and tearing and poor appearance during film formation are suppressed. If the inorganic filler is less than 35%, the void formability is lowered. On the other hand, if it exceeds 50 wt%, the void formability is improved, but the air permeability becomes excessive, and the inorganic filler is likely to fall off, pinholes, tears, and appearance defects during the stretching process.
本発明に用いる多孔質フィルムは、前記ポリエチレン樹脂および無機充填剤の特定範囲に配合することで、目的とするフィルム特性およびヒートシール性が得られる。つまり、直鎖状低密度ポリエチレンが40〜62wt%、高圧法の低密度ポリエチレンが2〜10wt%、無機充填剤が35〜50wt%からなる混合樹脂を2軸混練押出機などで混合分散させて好ましく用いられる。 When the porous film used in the present invention is blended in a specific range of the polyethylene resin and the inorganic filler, desired film characteristics and heat sealability can be obtained. That is, a mixed resin composed of 40 to 62 wt% of linear low density polyethylene, 2 to 10 wt% of high density low density polyethylene, and 35 to 50 wt% of inorganic filler is mixed and dispersed by a twin screw kneading extruder or the like. Preferably used.
本発明で用いる多孔質フィルムには、着色剤、老化防止剤、酸化防止剤、紫外線吸収剤、難燃剤および安定剤などの各種添加剤が、本発明の効果を損なわない範囲内で配合されていてもよい。 In the porous film used in the present invention, various additives such as a colorant, an antioxidant, an antioxidant, an ultraviolet absorber, a flame retardant and a stabilizer are blended within a range not impairing the effects of the present invention. May be.
本発明における多孔質フィルムは、溶融成膜法によって製造することができる。中でもTダイ法が好ましい。例えば、上記のポリオレフィン系樹脂、無機充填剤、及び、必要に応じて、各種添加剤を、2軸混練押出などで混合分散し、一旦ペレット状にした後、ギヤポンプ付き2軸混錬押出機にて溶融押出して未延伸フィルムを作製し、該未延伸フィルムを、1軸に延伸することにより多孔質化して製造する。 The porous film in the present invention can be produced by a melt film formation method. Of these, the T-die method is preferable. For example, the polyolefin resin, inorganic filler, and if necessary, various additives are mixed and dispersed by biaxial kneading extrusion, etc., once pelletized, and then into a biaxial kneading extruder with a gear pump. Then, an unstretched film is produced by melt extrusion, and the unstretched film is made porous by stretching uniaxially.
本発明で用いる多孔質フィルムの製法における特徴は、無機充填剤含有ポリエチレン系樹脂を一旦ペレット状にした後、ギヤポンプ付き2軸混錬押出機で再度混錬することで、樹脂中の無機充填剤が均一に混ざり、孔の分散性を向上させことができ、且つ、延伸加工することで微細な孔が生じ、細孔体積が大きくでき、好適なヒートシール性が得られ、熱シール時のエッジ切れを少なくできることである。
なお、多孔質フィルムには、充分な接着強度を得るために表面活性処理がなされていてもよく、必要に応じて帯電防止処理などの各種処理が施されていてもよい。
The feature of the method for producing the porous film used in the present invention is that the inorganic filler-containing polyethylene resin is once pelletized and then kneaded again with a twin-screw kneading extruder with a gear pump, so that the inorganic filler in the resin Can be uniformly mixed, the dispersibility of the pores can be improved, and fine pores can be produced by stretching, the pore volume can be increased, and a suitable heat-sealing property can be obtained. It is possible to reduce cutting.
The porous film may be subjected to surface activation treatment in order to obtain sufficient adhesive strength, and may be subjected to various treatments such as antistatic treatment as necessary.
上記多孔質フィルムの成型時において、押出温度は170〜270℃が好ましく、さらに好ましくは180〜260℃、特に好ましくは210〜250℃である。また、未延伸フィルム作製時の引き取り速度は5〜25m/分が好ましく、引き取りロール温度(冷却温度)は10 〜40℃が好ましく、さらに好ましくは20〜30℃である。 At the time of molding the porous film, the extrusion temperature is preferably 170 to 270 ° C, more preferably 180 to 260 ° C, and particularly preferably 210 to 250 ° C. Moreover, 5-25 m / min of the taking-up speed at the time of unstretched film preparation is preferable, 10-40 degreeC is preferable and the take-up roll temperature (cooling temperature) is 20-30 degreeC more preferably.
前記未延伸フィルムを1軸に延伸する方法としては、ロール延伸方式やテンター延伸方式など公知慣用の延伸方式を用いることができる。延伸温度は40〜100℃が好ましく、さらに好ましくは50〜80℃である。尚、カイロ発熱時の通気度の変化、カイロ製袋加工時のヒートシール温度などでの熱収縮を防止するために、5〜20%の緩和状態にて、フィルムの軟化点以上、融点以下の温度でのヒートセットが好ましい。多孔質化と安定成膜の観点から、延伸倍率(単軸方向)は3〜5倍が好ましく、さらに好ましくは3.5〜4.5倍である。
延伸倍率が3倍未満の場合は、微細孔のボイド発生が少なくなり、延伸ムラが発生し、透気度および透湿度がバラツキ、5倍を超えると、透気度および透湿度は高くできるが、無機充填剤の樹脂中からの脱落が発生し、貫通孔も生じ、通気度のバラツキが大きくなり、且つ、フィルムの配向が大きく製袋加工時のエッジ切れが生じやすくなる。
As a method for stretching the unstretched film uniaxially, a known and usual stretching method such as a roll stretching method or a tenter stretching method can be used. The stretching temperature is preferably 40-100 ° C, more preferably 50-80 ° C. In addition, in order to prevent heat shrinkage due to changes in air permeability during heat generation of the warmer, heat seal temperature during the bag making process, etc., in a relaxed state of 5 to 20%, the softening point of the film is equal to or higher than the melting point. Heat setting at temperature is preferred. From the viewpoint of making it porous and forming a stable film, the draw ratio (uniaxial direction) is preferably 3 to 5 times, and more preferably 3.5 to 4.5 times.
When the draw ratio is less than 3 times, the generation of voids in the micropores is reduced, the stretch unevenness occurs, and the air permeability and moisture permeability vary. When the draw ratio exceeds 5 times, the air permeability and moisture permeability can be increased. The inorganic filler is dropped from the resin, through holes are formed, the air permeability varies greatly, the orientation of the film is large, and the edges are easily cut during bag making.
本発明で用いる多孔質フィルムの坪量は40〜100g/m2であり、好ましくは45〜90g/m2、より好ましくは50〜80g/m2である。坪量が40g/m2以上であることにより、また、坪量が100g/m2以下であることにより、通気性、透湿性および製袋加工性が良好になる。坪量が40g/m2未満では、破れが起こり、また外観品位および微細孔のボイド形成性などが低下し、一方100g/m2を超えると、ピンホールはなくなり、外観品位などは良くなるが、硬くなり、ソフト感がなく、使用感が悪くなると共に高い価格になるので好ましくない。 The basis weight of the porous film used in the present invention is 40 to 100 g / m 2 , preferably 45 to 90 g / m 2 , more preferably 50 to 80 g / m 2 . When the basis weight is 40 g / m 2 or more, and when the basis weight is 100 g / m 2 or less, air permeability, moisture permeability, and bag-making processability are improved. If the basis weight is less than 40 g / m 2 , tearing occurs and appearance quality and void formation of fine holes are reduced. On the other hand, if it exceeds 100 g / m 2 , pinholes disappear and appearance quality is improved. It is not preferable because it becomes hard, does not have a soft feeling, becomes unusable and becomes expensive.
本発明に用いる多孔質フィルムは、細孔分布が0.025〜3.0μmの範囲における水銀圧入方による測定において、メディアン径が1.0μm以下、好ましくは0.2〜0.6μm、より好ましくは0.3〜0.5μmである。また、細孔体積は0.30ml/g以上、好ましくは0.40〜0.60ml/g、より好ましくは0.45〜0.60ml/gである。細孔比表面積は5.0m2/g以上が好ましく、さらに好ましくは5.5〜10m2/g、特に好ましくは、6.0〜10m2/gである。この領域の細孔分布測定値のメディアン径、細孔体積および細孔表面積が上記の範囲であると、孔の構成は小さいボイドが多数存在する構成となり、通気性および透湿性のバラツキを小さくできる。従って、使い捨てカイロの小さいサイズにおいても、均等な通気性および透湿性が得られ、カイロの特性の最高発熱温度および発熱持続時間などが良好となる。 The porous film used in the present invention has a median diameter of 1.0 μm or less, preferably 0.2 to 0.6 μm, more preferably, as measured by mercury intrusion in a pore distribution range of 0.025 to 3.0 μm. Is 0.3 to 0.5 μm. The pore volume is 0.30 ml / g or more, preferably 0.40 to 0.60 ml / g, more preferably 0.45 to 0.60 ml / g. The pore specific surface area is preferably 5.0 m 2 / g or more, more preferably 5.5 to 10 m 2 / g, and particularly preferably 6.0 to 10 m 2 / g. When the median diameter, pore volume, and pore surface area of the pore distribution measurement value in this region are in the above ranges, the pore configuration has many small voids, and variation in air permeability and moisture permeability can be reduced. . Therefore, even in the small size of the disposable body warmer, uniform air permeability and moisture permeability can be obtained, and the maximum heat generation temperature and heat generation duration of the body warming characteristics are improved.
本発明に用いる多孔質フィルムの10%伸長時の応力は5N/10mm以上であり、好ましくは6〜15N/10mm、より好ましくは7〜12N/10mmである。10%伸長時の応力が高いことは、多孔質フィルムと不織布とを貼り合わせる際の張力などによるフィルムの伸長が起こり難くなる為、カイロ製品の通気性および透湿性に対する加工操作による影響を少なくできる。 The stress at the time of 10% elongation of the porous film used in the present invention is 5 N / 10 mm or more, preferably 6 to 15 N / 10 mm, more preferably 7 to 12 N / 10 mm. The high stress at 10% elongation makes it difficult for the film to stretch due to tension when the porous film and the nonwoven fabric are bonded to each other, so the influence of processing operations on the air permeability and moisture permeability of the warmer product can be reduced. .
本発明で用いる多孔質フィルムの王研式透気度は500〜15000秒/100ccが好ましく、さらに好ましくは700〜10000秒/100cc、特に好ましくは800〜8000秒/100ccである。また、透湿度は500〜2000g/m2/24hrが好ましく、さらに好ましくは500〜1800g/m2/24hr、特に好ましくは600〜1500g/m2/24hrである。該フィルムの透気度および透湿度がこの範囲であれば、不織布と接着剤で貼り合わせて通気性積層体とした際に、得られる通気性積層体の通気性および透湿性を目的の範囲にすることが可能である。
透気度が500秒/100cc未満または透湿度が500g/m2/24hr未満では、得られた通気性積層体をカイロ製品にした時に、最高温度、安定温度、持続時間などが使用できる範囲外となる場合が生じる。
The Oken type air permeability of the porous film used in the present invention is preferably 500 to 15000 seconds / 100 cc, more preferably 700 to 10000 seconds / 100 cc, and particularly preferably 800 to 8000 seconds / 100 cc. Further, the moisture permeability is preferably from 500~2000g / m 2 / 24hr, more preferably 500~1800g / m 2 / 24hr, particularly preferably 600~1500g / m 2 / 24hr. If the air permeability and moisture permeability of the film are within this range, the breathability and moisture permeability of the resulting breathable laminate will be within the intended ranges when bonded with a nonwoven fabric and an adhesive to form a breathable laminate. Is possible.
The air permeability is less than 500 seconds / 100 cc or less than moisture permeability of 500g / m 2 / 24hr, the resulting breathable laminate when Cairo product, outside the range maximum temperature, such as the stable temperature, duration can be used May occur.
本発明において前記不織布と前記多孔質フィルムとを積層する方法としては、接着剤を介して貼り合わせる方法が好ましい。用いる接着剤は、得られる通気性積層体の透気度および透湿度を後述する範囲に制御できるものであれば特に限定されず、不織布と多孔質フィルムの貼り合わせなどに用いられる公知の接着剤を用いることができる。
例えば、ゴム系(天然ゴム、スチレン系エラストマーなど)、ウレタン系(アクリルウレタン系)、ポリオレフィン系(エチレン−酢酸ビニル共重合体(EVA)、エチレン−アクリル酸メチル共重合体(EMA)等)、アクリル系、シリコーン系、ポリエステル系、ポリアミド系、エポキシ系、ビニルアルキルエーテル系およびフッ素系などの公知の接着剤を用いることができる。また、上記接着剤は単独で又は2種以上を組み合わせて用いることができる。上記の中でも、2液型のポリエステル系樹脂およびポリウレタン系樹脂が好ましい。
In the present invention, the method of laminating the nonwoven fabric and the porous film is preferably a method of laminating via an adhesive. The adhesive to be used is not particularly limited as long as the air permeability and moisture permeability of the obtained breathable laminate can be controlled within the ranges described below, and a known adhesive used for bonding a nonwoven fabric and a porous film, etc. Can be used.
For example, rubber-based (natural rubber, styrene-based elastomer, etc.), urethane-based (acrylic urethane-based), polyolefin-based (ethylene-vinyl acetate copolymer (EVA), ethylene-methyl acrylate copolymer (EMA), etc.), Known adhesives such as acrylic, silicone, polyester, polyamide, epoxy, vinyl alkyl ether, and fluorine can be used. Moreover, the said adhesive agent can be used individually or in combination of 2 or more types. Among these, two-component polyester resins and polyurethane resins are preferable.
また、接着剤は、いずれの形態を有している接着剤であってもよく、特に限定されないが、2液型ウレタン樹脂などの反応型樹脂を用いるドライラミネート法などが好ましい。
さらに、熱により溶融させることにより塗工することができ、不織布に対しても直接塗布して接着剤層を形成することができる利点、ヒートシール部ではヒートシール加工によって更に大きな接着力が得られる利点を有することから、ホットメルト型(熱溶融型)接着剤が好適に用いられる。このような接着剤としては、ポリアミド系又はポリエステル系のホットメルト型接着剤が好ましく、熱可塑性ポリアミド系ホットメルト型接着剤、又は、熱可塑性ポリエステル系ホットメルト型接着剤がより好ましい。
Further, the adhesive may be an adhesive having any form, and is not particularly limited, but a dry laminating method using a reactive resin such as a two-component urethane resin is preferable.
Furthermore, it can be applied by melting by heat, and can be applied directly to a non-woven fabric to form an adhesive layer. In the heat-sealed part, a larger adhesive force can be obtained by heat-sealing. Since it has an advantage, a hot melt type (hot melt type) adhesive is preferably used. As such an adhesive, a polyamide-based or polyester-based hot-melt adhesive is preferable, and a thermoplastic polyamide-based hot-melt adhesive or a thermoplastic polyester-based hot-melt adhesive is more preferable.
不織布と多孔質フィルムとの具体的な積層方法としては、接着剤の種類などによっても異なり、特に限定されないが、2液型のポリエステル系樹脂またはウレタン系樹脂等の接着剤をグラビアロールで多孔質フィルム面に塗布した後、積層して接着させるドライラミネートなどが好ましく用いられる。この場合、接着剤の塗布面積が接着強度、通気性および透湿性に影響することから、グラビア版の形状および非接合面積率を考慮する必要がある。例えば、グラビア版は、斜め格子柄などがドクターのかき落し性の点で好ましい。また、不織布とフィルムとの接合面積率が通気性積層体の通気性および透湿性に影響するので、非接合面積率は15〜55%が好ましく、さらに好ましくは20〜50%である。非接合面積率が15%未満では、高い接着力は得られるが、通気性および透気性が低下する。一方、55%を超えると、通気性および透湿性は向上するが、接着力が低下する。
また、ホットメルト型接着剤を用いる場合には、接着剤を不織布上に塗布した後、多孔質フィルムを貼り合わせる方法が好ましく用いられる。ホットメルト型接着剤の塗布方法として用いられる公知慣用の方法を用いることが可能であり、特に限定されないが、例えば、通気性を維持する観点から、スプレー塗布による塗布、ストライプ塗工、ドット塗工が好ましい。
The specific method of laminating the nonwoven fabric and the porous film varies depending on the type of the adhesive and is not particularly limited. However, the adhesive such as a two-component polyester resin or urethane resin is porous with a gravure roll. A dry laminate or the like that is applied to the film surface and then laminated and adhered is preferably used. In this case, since the application area of the adhesive affects the adhesive strength, air permeability and moisture permeability, it is necessary to consider the shape of the gravure plate and the non-bonded area ratio. For example, the gravure plate is preferably a diagonal lattice pattern from the viewpoint of scratching by the doctor. Further, since the bonding area ratio between the nonwoven fabric and the film affects the air permeability and moisture permeability of the air-permeable laminate, the non-bonding area ratio is preferably 15 to 55%, more preferably 20 to 50%. When the non-bonded area ratio is less than 15%, high adhesive strength can be obtained, but air permeability and air permeability are reduced. On the other hand, if it exceeds 55%, the air permeability and moisture permeability are improved, but the adhesive strength is lowered.
Moreover, when using a hot-melt-type adhesive agent, the method of bonding a porous film after apply | coating an adhesive agent on a nonwoven fabric is used preferably. It is possible to use a known and commonly used method used as a hot melt adhesive coating method, and it is not particularly limited. For example, from the viewpoint of maintaining air permeability, application by spray coating, stripe coating, dot coating Is preferred.
接着剤の塗布量(固形分)は、特に限定されないが、袋体形成時のヒートシール部の接着性と経済性の観点から、2〜10g/m2が好ましく、より好ましくは3〜8g/m2である。
また、不織布と多孔質フィルムとの接合強度は1N/25mm以上が好ましく、さらに好ましくは2〜15N/25mm、特に好ましくは3〜15N/25mmである。接合強度が1N/25mm未満の場合は、通気性積層体の取扱い中および製品カイロの使用中などで剥離する場合がある。
Although the application amount (solid content) of the adhesive is not particularly limited, it is preferably 2 to 10 g / m 2 , more preferably 3 to 8 g / m 2 from the viewpoints of adhesiveness and economical efficiency of the heat seal part during bag formation. m 2 .
Further, the bonding strength between the nonwoven fabric and the porous film is preferably 1 N / 25 mm or more, more preferably 2 to 15 N / 25 mm, and particularly preferably 3 to 15 N / 25 mm. When the bonding strength is less than 1 N / 25 mm, peeling may occur during handling of the breathable laminate and use of the product warmer.
本発明の通気性積層体の王研式透気度は5000〜240000秒/100cc、好ましくは7000〜90000秒/100ccであり、透湿度は200〜800g/m2/24hrであることが好ましく、さらに好ましくは300〜750g/m2/24hrである。透気度および透湿度がこの範囲であれば、使い捨てカイロ製品の最高温度、安定温度、持続時間を適正範囲にできるので好ましい。一方、透気度および透湿性がこの範囲外では、使い捨てカイロ製品のこれらの特性を適正範囲にすることが困難である。 OKen ShikiToru air permeability of breathable laminate of the present invention is from 5000 to 240000 seconds / 100 cc, preferably from 7000 to 90000 sec / 100 cc, the moisture permeability is preferably from 200~800g / m 2 / 24hr, More preferably, it is 300-750 g / m < 2 > / 24hr. If the air permeability and moisture permeability are in this range, it is preferable because the maximum temperature, stable temperature, and duration of the disposable body warmer product can be within appropriate ranges. On the other hand, when the air permeability and moisture permeability are out of this range, it is difficult to bring these characteristics of the disposable body warmer products into an appropriate range.
本発明の通気性積層体を用いた使い捨てカイロは、袋体即ち通気性積層体の透気度および透湿度、並びに発熱組成物の充填量および配合などにより、最高温度、安定温度および持続時間の調整が可能である。具体的には、袋体の通気性を小さくすることで、最高温度を下げることができる。また透湿度を小さくすることで、発熱反応を遅延し、持続時間を長くできる。更に、発熱組成物の充填量が少ないと、持続時間が短い使い捨てカイロが得られる。 The disposable body warmer using the breathable laminate of the present invention has a maximum temperature, a stable temperature and a duration depending on the air permeability and moisture permeability of the bag body, that is, the breathable laminate, and the filling amount and blending of the exothermic composition. Adjustment is possible. Specifically, the maximum temperature can be lowered by reducing the air permeability of the bag. Further, by reducing the moisture permeability, the exothermic reaction can be delayed and the duration can be increased. Furthermore, when the filling amount of the exothermic composition is small, a disposable body warmer having a short duration can be obtained.
貼るカイロとしては、袋体の片面に本発明の通気性積層体を用い、他面に非通気性のフィルムまたは、非通気性のフィルムと不織布の積層体を用いる構成にし、非通気性面に粘着性樹脂を塗布し、離型紙を貼り、鉄分、活性炭、バーミキュライト、水および塩類を含有する発熱組成物を袋体に充填して、周囲を封止して得られる。
なお、本発明のカイロの最高温度、安定温度および持続時間の適正範囲は、それぞれ50〜65℃、40〜60℃および8〜15時間とした。
As the warmer to be applied, the breathable laminate of the present invention is used on one side of the bag, and the non-breathable film or the laminate of the non-breathable film and the nonwoven fabric is used on the other side. It is obtained by applying an adhesive resin, pasting a release paper, filling a bag with a heat generating composition containing iron, activated carbon, vermiculite, water and salts, and sealing the periphery.
The appropriate ranges of the maximum temperature, stable temperature, and duration of the warmer of the present invention were 50 to 65 ° C., 40 to 60 ° C., and 8 to 15 hours, respectively.
以下、本発明を実施に基づいて説明するが、本発明はこれらの実施例のみに限定されるものではない。本発明における各特性値の測定方法は以下の通りである。
(1)坪量(g/m2):タテ20cm×ヨコ25cmの試料を任意に3か所切り取り、重量を測定し、その平均値を単位面積当たりの重量に換算して求めた。
(2)厚み(mm):荷重10kpa下で、任意に10か所測定し、平均値を求めた。
Hereinafter, although this invention is demonstrated based on implementation, this invention is not limited only to these Examples. The measuring method of each characteristic value in the present invention is as follows.
(1) Basis weight (g / m 2 ): A sample of length 20 cm × width 25 cm was arbitrarily cut out at three places, the weight was measured, and the average value was calculated by converting the weight per unit area.
(2) Thickness (mm): Ten points were measured arbitrarily under a load of 10 kpa, and an average value was obtained.
(3)10%伸長時の応力(N/10mm):ヨコ方向10mm、タテ方向(MD方向)200mmの試料を任意に3枚採取し、JIS−L−1913に準じて定長引張試験機を用いて、つかみ間隔10cm、引張速度100mm/分で測定し、タテ方向の10%伸長時の応力を3枚の平均値で求めた。 (3) Stress at 10% elongation (N / 10 mm): Three samples of 10 mm in the horizontal direction and 200 mm in the vertical direction (MD direction) are taken arbitrarily, and a constant-length tensile testing machine is used according to JIS-L-1913. It was measured at a grip interval of 10 cm and a tensile speed of 100 mm / min, and the stress at the time of 10% elongation in the vertical direction was obtained as an average value of three sheets.
(4)王研式透気度(秒/100cc):旭精工(株)製KR−1−8−7MRの王研式透気度測定機で測定する(JIS−P−8117に準じる)。測定値は3か所の平均値で示す。
また、透気度変化率はもみモデルテスト前後の変化率として下記の如く求めた。
もみモデルテスト後の測定として、積層体からタテ15cmヨコ15cmの正方形のサンプルを切り取り、引張試験機を用い、つかみ間隔10cm、引張速度10cm/分の条件で、伸長率5%および10%に設定して、タテ方向、ヨコ方向の両方向に10回伸長を繰り返すもみモデルテストを行ない、テスト前後の透気度から次式によって透気度の変化率を求めた。
透気度変化率(%)=[(テスト前−テスト後)/(テスト前)]×100
(4) Oken Air Permeability (sec / 100 cc): Measured with KR-1-8-7MR Oken Air Permeability Measuring Machine manufactured by Asahi Seiko Co., Ltd. (according to JIS-P-8117). The measured value is shown as an average value at three locations.
Further, the air permeability change rate was obtained as follows as the change rate before and after the fir model test.
As a measurement after the fir model test, a square sample of 15 cm in length and 15 cm in width is cut out from the laminate, and stretch rate is set to 5% and 10% using a tensile tester under the conditions of a holding interval of 10 cm and a pulling speed of 10 cm / min. Then, a paddy model test was repeated 10 times in both the vertical and horizontal directions, and the change rate of the air permeability was calculated from the air permeability before and after the test according to the following equation.
Permeability change rate (%) = [(before test−after test) / (before test)] × 100
(5)透湿度(g/m2/24hr):JIS−L−1099に準じてカップ法にて測定する(乾燥剤:塩化カルシュウム 15g)。 (5) moisture permeability (g / m 2 / 24hr) : in accordance with JIS-L-1099 is measured by the cup method (desiccant: calcium chloride 15 g).
(6)細孔分布:水銀圧入法による細孔分布測定を行なう。
島津製作所−マイクロメリテックス社製細孔分布測定装置(9250型)を使用。
試料は、各12.5mm×25mmに裁断し、折り畳み、標準5ccセルに採り、初期圧20kPaの条件で測定した。水銀パラメーターは水銀接触角130度、水銀表面張力485ダイン/cmに設定して測定した。
<メディアン径>:積算細孔分布のY軸の最小値と最大値の中間に相当するX軸値を意味する。
<細孔体積>:測定時の最大圧力までに水銀が圧入された細孔体積の積算値を試料重量で割った値。
<細孔表面積>:細孔形状が幾何学的な円筒であると仮定した細孔の表面積で、測定範囲内における圧力と圧入された水銀量の関係から計算された値。
(6) Pore distribution: The pore distribution is measured by mercury porosimetry.
Uses a pore distribution measuring device (Type 9250) manufactured by Shimadzu Corporation-Micromeritex Corporation.
Each sample was cut into 12.5 mm × 25 mm, folded, taken in a standard 5 cc cell, and measured under conditions of an initial pressure of 20 kPa. Mercury parameters were measured at a mercury contact angle of 130 degrees and a mercury surface tension of 485 dynes / cm.
<Median diameter>: Means an X-axis value corresponding to an intermediate value between the minimum value and the maximum value of the Y-axis of the integrated pore distribution.
<Pore volume>: A value obtained by dividing the integrated value of the pore volume into which mercury has been injected up to the maximum pressure at the time of measurement by the sample weight.
<Pore surface area>: The surface area of a pore assumed to have a geometric cylindrical shape, calculated from the relationship between the pressure in the measurement range and the amount of mercury injected.
(7)部分熱圧着率(エンボス面積比率):不織布の表面を、マイクロスコープ(倍率20倍)により観察し、測定領域(10mm(MD方向)×10mm(TD方向))中のエンボス加工部分の面積の割合(面積%)を計測(計算)し、エンボス面積比率とした(下記式)。
エンボス面積比率(%)=エンボス加工部分の面積(mm2)/100×100
なお、不織布の片面について測定(n=5)を行い、平均値を当該不織布のエンボス面積比率とした。
(7) Partial thermocompression bonding ratio (embossed area ratio): The surface of the nonwoven fabric was observed with a microscope (magnification 20 times), and the embossed part in the measurement region (10 mm (MD direction) × 10 mm (TD direction)) The area ratio (area%) was measured (calculated) and used as the embossed area ratio (the following formula).
Embossed area ratio (%) = area of embossed part (mm 2 ) / 100 × 100
In addition, it measured about the single side | surface of the nonwoven fabric (n = 5), and made the average value the embossed area ratio of the said nonwoven fabric.
(8)接合強度(N/25mm):JIS−K−6854−3のT型剥離に準じる。
幅25mm×長さ200mmの通気性積層体サンプルをタテ方向から3枚採取し、定長引張試験機を用い、引張速度100mm/分、つかみ間隔50mmで剥離強度を測定して、平均値で示す。
(8) Bonding strength (N / 25 mm): Conforms to T-type peeling according to JIS-K-6854-3.
Three samples of a breathable laminate having a width of 25 mm and a length of 200 mm were taken from the vertical direction, and the peel strength was measured at a tensile speed of 100 mm / min and a gripping interval of 50 mm using a constant length tensile tester, and the average value is shown. .
(9)シール強度(N/15mm):熱シール機を用いて、シールバー上下の表面温度を150℃にし、シール幅5mm、圧力2kg/cm2、時間1秒にて通気性積層体サンプルの熱シールを行なった後、タテ方向及びヨコ方向から、幅15mm×長さ100mmの試料を3枚ずつ採取し、定長引張試験機を用い、引張速度300mm/分、つかみ間隔30mmで剥離強度を測定して、平均値で示す。 (9) Seal strength (N / 15 mm): Using a heat sealing machine, the surface temperature above and below the seal bar is set to 150 ° C., the seal width is 5 mm, the pressure is 2 kg / cm 2 , and the time is 1 second. After heat-sealing, three samples each having a width of 15 mm and a length of 100 mm were taken from the vertical direction and the horizontal direction, and using a constant-length tensile tester, the peel strength was measured at a pulling speed of 300 mm / min and a grip interval of 30 mm. Measured and shown as an average value.
(10)カイロの作成:通気性積層体と、不織布および非通気性フィルム(LLDPE70μm)の積層体とから各々幅95mm×長さ130mmの試料を切り取り、内側で多孔質フィルムと非通気性フィルムが合わさるようにして、3方向を熱シールして袋体を作り、該袋体に使い捨てカイロ用発熱組成物(鉄分、活性炭、バーミキュライト、水、塩類を含有する発熱組成物)を40g入れ、JIS−S−4100に準じて、表面温度、持続時間などを測定して、カイロ仕様の評価を行った(熱シール条件:シール幅5mm、温度150℃、時間1秒)。 (10) Preparation of warmers: Samples each having a width of 95 mm and a length of 130 mm are cut from a breathable laminate and a laminate of a nonwoven fabric and a non-breathable film (LLDPE 70 μm), and a porous film and a non-breathable film are formed inside. Make a bag by heat-sealing in three directions, and put 40 g of a heat-generating composition for disposable body warmers (a heat-generating composition containing iron, activated carbon, vermiculite, water and salts) into the bag, and JIS- In accordance with S-4100, surface temperature, duration, etc. were measured to evaluate the warmer specifications (heat seal conditions: seal width 5 mm, temperature 150 ° C., time 1 second).
(11)製袋加工性:上記(11)における製袋加工時の破れ、エッジ切れ、およびシール不良を目視観察し、下記基準で評価した。
○:製袋加工時の破れ、エッジ切れ、シール不良がない。
△:製袋加工時のエッジ切れが少し生じる,程度である。
×:製袋加工時の破れ、エッジ切れ、シール不良が多く発生する。
(11) Bag-making processability: The tear, edge breakage, and seal failure during bag-making process in (11) above were visually observed and evaluated according to the following criteria.
○: No tearing, edge breakage, or sealing failure during bag making.
(Triangle | delta): It is a grade which the edge cut | disconnection at the time of bag making process arises a little.
X: Many tears, edge breaks, and poor seals occur during bag making.
[実施例1]
不織布としては、スパンボンド方式により製造されたポリエステル長繊維不織布(エンボス面積比率11%、目付け25g/m2)を用いた。なお、上記不織布のエンボス1個当たりの面積は1.0mm2である。
メタロセン触媒の直鎖状低密度ポリエチレン(ダウケミカル社製、密度0.915、MFR(190℃)3.5g/10分)49wt%、高圧法の低密度ポリエチレン5wt%、炭酸カルシウム(D=50%、4μm)45wt%、ステアリン酸および酸化防止剤が合計で1wt%からなる樹脂混合物を220℃で溶融混練し、混合原料を得た。得られた混合原料を用い、ギヤポンプ付き2軸混錬押出機により、Tダイ法で溶融押出し、未延伸フィルムを得た。得られた未延伸フィルムを温度60℃で加熱し、延伸倍率4.2倍に延伸加工して、本発明に用いる1軸延伸の坪量60g/m2のポリエチレン系多孔質フィルムを得た。表1に不織布および多孔質フィルムの特性を示す。
[Example 1]
As the non-woven fabric, a polyester long-fiber non-woven fabric manufactured by a spunbond method (embossed area ratio 11%, basis weight 25 g / m 2 ) was used. In addition, the area per emboss of the said nonwoven fabric is 1.0 mm < 2 >.
Metallocene catalyst linear low density polyethylene (Dow Chemical Co., density 0.915, MFR (190 ° C.) 3.5 g / 10 min) 49 wt%, high pressure low density polyethylene 5 wt%, calcium carbonate (D = 50 %, 4 μm) 45 wt%, and a resin mixture consisting of 1 wt% in total of stearic acid and antioxidant was melt kneaded at 220 ° C. to obtain a mixed raw material. The obtained mixed raw material was melt-extruded by a T-die method using a twin-screw kneading extruder with a gear pump to obtain an unstretched film. The obtained unstretched film was heated at a temperature of 60 ° C. and stretched to a stretch ratio of 4.2 times to obtain a polyethylene-based porous film having a basis weight of 60 g / m 2 for uniaxial stretching used in the present invention. Table 1 shows the characteristics of the nonwoven fabric and the porous film.
次いで、これらの不織布と多孔質フィルムとを2液型ポリエステル系樹脂を用い、非接合面積率が19%の斜め格子柄グラビア版で、多孔質フィルム面に接着剤を途布して、ドライラミネート法で貼り合わせ、本発明の通気性積層体を得た。さらに、得られた通気性積層体を用いてカイロを作製し、その評価を行なった。表2に通気性積層体およびカイロの特性を示す。表2から、得られた使い捨てカイロの最高温度、安定温度および持続時間などは適正範囲であることが分かる。 Next, these nonwoven fabrics and porous films are slanted lattice gravure plates with a non-bonded area ratio of 19% using a two-component polyester resin, and an adhesive is spread on the porous film surface to dry laminate. The breathable laminated body of the present invention was obtained by laminating by the method. Furthermore, a warmer was produced using the obtained air-permeable laminate and evaluated. Table 2 shows the characteristics of the breathable laminate and the body warmer. From Table 2, it can be seen that the maximum temperature, the stable temperature, the duration, and the like of the obtained disposable body warmer are in an appropriate range.
[実施例2]
不織布としては、スパンボンド方式により製造されたポリアミド長繊維不織布(エンボス面積比率6%、目付け40g/m2)を用いた。なお、上記不織布のエンボス1個当たりの面積は0.14mm2である。
メタロセン触媒の直鎖状低密度ポリエチレン(ダウケミカル社製、密度0.915、MFR(190℃)3.5g/10分)53wt%、高圧法の低密度ポリエチレン5wt%、炭酸カルシウム(D=50%、4μm)41wt%、ステアリン酸および酸化防止剤が合計で1wt%からなる樹脂混合物を220℃で溶融混練し、混合原料を得た。得られた混合原料を用い、ギヤポンプ付き2軸混錬押出機により、Tダイ法で溶融押出し、未延伸フィルムを得た。得られた未延伸フィルムを温度60℃で加熱し、延伸倍率4.5倍に延伸加工して、本発明に用いる1軸延伸の坪量60g/m2のポリエチレン系多孔質フィルムを得た。表1に不織布および多孔質フィルムの特性を示す。
[Example 2]
As the nonwoven fabric, a polyamide long fiber nonwoven fabric (embossed area ratio 6%, basis weight 40 g / m 2 ) manufactured by a spunbond method was used. In addition, the area per emboss of the said nonwoven fabric is 0.14 mm < 2 >.
Metallocene catalyst linear low density polyethylene (Dow Chemical Co., density 0.915, MFR (190 ° C.) 3.5 g / 10 min) 53 wt%, high pressure low density polyethylene 5 wt%, calcium carbonate (D = 50) %, 4 μm) 41 wt%, and a resin mixture consisting of 1 wt% in total of stearic acid and antioxidant was melt kneaded at 220 ° C. to obtain a mixed raw material. The obtained mixed raw material was melt-extruded by a T-die method using a twin-screw kneading extruder with a gear pump to obtain an unstretched film. The obtained unstretched film was heated at a temperature of 60 ° C. and stretched to a stretch ratio of 4.5 times to obtain a uniaxially stretched polyethylene-based porous film having a basis weight of 60 g / m 2 used in the present invention. Table 1 shows the characteristics of the nonwoven fabric and the porous film.
次いで、これらの不織布と多孔質フィルムとを2液型ポリエステル系樹脂を用い、非接合面積率が42%の斜め格子柄グラビア版で、多孔質フィルム面に接着剤を途布して、ドライラミネート法で貼り合わせ、本発明の通気性積層体を得た。さらに、得られた通気性積層体を用いてカイロを作製し、その評価を行なった。表2に通気性積層体およびカイロの特性を示す。表2から、得られた使い捨てカイロの最高温度、安定温度および持続時間などは適正範囲であることが分かる。 Next, these nonwoven fabrics and porous films are slanted lattice gravure plates with a non-bonded area ratio of 42% using a two-component polyester resin, and an adhesive is spread on the porous film surface to dry laminate. The breathable laminated body of the present invention was obtained by laminating by the method. Furthermore, a warmer was produced using the obtained air-permeable laminate and evaluated. Table 2 shows the characteristics of the breathable laminate and the body warmer. From Table 2, it can be seen that the maximum temperature, the stable temperature, the duration, and the like of the obtained disposable body warmer are in an appropriate range.
[実施例3]
実施例1の不織布と多孔質フィルムとを用いて、下記の如く接合面積の異なる通気性積層体を得た。実施例1と同様の樹脂の2液型ポリエステル系樹脂を用い、非接合面積率が36%の斜め格子柄グラビア版で、多孔質フィルム面に接着剤を途布して、ドライラミネート法で貼り合わせ、本発明の通気性積層体を得た。さらに、得られた通気性積層体を用いてカイロを作製し、その評価を行なった。表2に通気性積層体およびカイロの特性を示す。表2から、得られた使い捨てカイロの最高温度、安定温度および持続時間などは適正範囲であることが分かる。
[Example 3]
Using the nonwoven fabric and porous film of Example 1, breathable laminates having different bonding areas were obtained as follows. Using a two-component polyester resin of the same resin as in Example 1, an oblique lattice pattern gravure plate with a non-bonded area ratio of 36%, and an adhesive is distributed on the porous film surface and pasted by a dry laminate method In addition, a breathable laminate of the present invention was obtained. Furthermore, a warmer was produced using the obtained air-permeable laminate and evaluated. Table 2 shows the characteristics of the breathable laminate and the body warmer. From Table 2, it can be seen that the maximum temperature, the stable temperature, the duration, and the like of the obtained disposable body warmer are in an appropriate range.
[実施例4]
メタロセン触媒の直鎖状低密度ポリエチレン(ダウケミカル社製、密度0.915、MFR(190℃)3.5g/10分)55wt%、高圧法の低密度ポリエチレン3wt%、炭酸カルシウム(D=50%、4μm)41wt%、ステアリン酸および酸化防止剤が合計で1wt%からなる樹脂混合物を220℃で溶融混練し、混合原料を得た。得られた混合原料を用い、ギヤポンプ付き2軸混錬押出機により、Tダイ法で溶融押出し、未延伸フィルムを得た。得られた未延伸フィルムを温度60℃で加熱し、延伸倍率4.5倍に延伸加工して、本発明に用いる1軸延伸の坪量60g/m2のポリエチレン系多孔質フィルムを得た。得られた多孔質フィルムの特性を表1に示す。
[Example 4]
Metallocene catalyst linear low density polyethylene (Dow Chemical Co., density 0.915, MFR (190 ° C.) 3.5 g / 10 min) 55 wt%, high pressure method low density polyethylene 3 wt%, calcium carbonate (D = 50 %, 4 μm) 41 wt%, and a resin mixture consisting of 1 wt% in total of stearic acid and antioxidant was melt kneaded at 220 ° C. to obtain a mixed raw material. The obtained mixed raw material was melt-extruded by a T-die method using a twin-screw kneading extruder with a gear pump to obtain an unstretched film. The obtained unstretched film was heated at a temperature of 60 ° C. and stretched to a stretch ratio of 4.5 times to obtain a uniaxially stretched polyethylene-based porous film having a basis weight of 60 g / m 2 used in the present invention. The properties of the obtained porous film are shown in Table 1.
次いで、得られた多孔質フィルムと実施例2に記載の不織布とを2液型ポリエステル系樹脂を用い、非接合面積率が36%の斜め格子柄グラビア版で、多孔質フィルム面に接着剤を途布して、ドライラミネート法で貼り合わせ、本発明の通気性積層体を得た。さらに、得られた通気性積層体を用いてカイロを作製し、その評価を行なった。表2に通気性積層体およびカイロの特性を示す。表2から、得られた使い捨てカイロの最高温度、安定温度および持続時間などは適正範囲であることが分かる。 Next, the obtained porous film and the nonwoven fabric described in Example 2 were used in a two-part polyester resin, and an oblique lattice pattern gravure plate with a non-bonded area ratio of 36%, and an adhesive was applied to the porous film surface. This was spread and bonded by a dry laminating method to obtain a breathable laminate of the present invention. Furthermore, a warmer was produced using the obtained air-permeable laminate and evaluated. Table 2 shows the characteristics of the breathable laminate and the body warmer. From Table 2, it can be seen that the maximum temperature, the stable temperature, the duration, and the like of the obtained disposable body warmer are in an appropriate range.
[実施例5]
メタロセン触媒の直鎖状低密度ポリエチレン(ダウケミカル社製、密度0.915、MFR(190℃)3.5g/10分)54wt%、高圧法の低密度ポリエチレン5wt%、炭酸カルシウム(D=50%、7μm)40wt%、ステアリン酸および酸化防止剤が合計で1wt%からなる混合樹脂を220℃で溶融混練し、混合原料を得た。得られた混合原料を用い、ギヤポンプ付き2軸混錬押出機により、Tダイ法で溶融押出し、未延伸フィルムを得た。得られた未延伸フィルムを温度60℃で加熱し、延伸倍率4.5倍に延伸加工して、本発明に用いる1軸延伸の坪量70g/m2のポリエチレン系多孔質フィルムを得た。得られた多孔質フィルムの特性を表1に示す。
[Example 5]
Metallocene catalyst linear low density polyethylene (Dow Chemical Co., density 0.915, MFR (190 ° C.) 3.5 g / 10 min) 54 wt%, high pressure low density polyethylene 5 wt%, calcium carbonate (D = 50) %, 7 μm) 40 wt%, a mixed resin consisting of 1 wt% in total of stearic acid and antioxidant was melt kneaded at 220 ° C. to obtain a mixed raw material. The obtained mixed raw material was melt-extruded by a T-die method using a twin-screw kneading extruder with a gear pump to obtain an unstretched film. The obtained unstretched film was heated at a temperature of 60 ° C. and stretched to a stretch ratio of 4.5 times to obtain a uniaxially stretched polyethylene-based porous film having a basis weight of 70 g / m 2 used in the present invention. The properties of the obtained porous film are shown in Table 1.
次いで、得られた多孔質フィルムと実施例1に記載の不織布とを2液型ポリエステル系樹脂を用い、非接合面積率が52%の斜め格子柄グラビア版で、多孔質フィルム面に接着剤を途布して、ドライラミネート法で貼り合わせ、本発明の通気性積層体を得た。さらに、得られた通気性積層体を用いてカイロを作製し、その評価を行なった。表2に通気性積層体およびカイロの特性を示す。表2から、得られた使い捨てカイロの最高温度、安定温度および持続時間などは適正範囲であることが分かる。 Next, the obtained porous film and the nonwoven fabric described in Example 1 were used in a two-part polyester resin, and an oblique lattice pattern gravure plate having a non-bonded area ratio of 52%, and an adhesive was applied to the porous film surface. This was spread and bonded by a dry laminating method to obtain a breathable laminate of the present invention. Furthermore, a warmer was produced using the obtained air-permeable laminate and evaluated. Table 2 shows the characteristics of the breathable laminate and the body warmer. From Table 2, it can be seen that the maximum temperature, the stable temperature, the duration, and the like of the obtained disposable body warmer are in an appropriate range.
本発明の通気性積層体は、多孔質フィルムと不織布を適切な接着面積率で接合し、透気度を特定範囲にすることで、使い捨てカイロに用いた場合、最高温度、安定温度、持続時間が適正範囲にでき、使い捨てカイロの製品化ができ、且つ、製袋加工時の破れ、エッジ切れ、シール不良などなく、収率よく製品が得られた。 The breathable laminate of the present invention has a maximum temperature, a stable temperature, and a duration when used in a disposable body warmer by bonding a porous film and a nonwoven fabric with an appropriate adhesion area ratio and making the air permeability within a specific range. Can be made into an appropriate range, and a disposable hand warmer can be commercialized, and the product is obtained in high yield without tearing, edge breakage, and defective sealing during bag making.
[比較例1]
メタロセン触媒の直鎖状低密度ポリエチレン(ダウケミカル社製、密度0.915、MFR(190℃)3.5g/10分)62wt%、高圧法の低密度ポリエチレン5wt%、炭酸カルシウム(D=50%、4μm)32wt%、ステアリン酸および酸化防止剤が合計で1wt%からなる混合樹脂を220℃で溶融混練し、混合原料とした以外は実施例1と同様の方法で多孔質フィルムを得た。得られた多孔質フィルムの特性を表1に示す。
次いで、得られた多孔質フィルムと実施例1に記載の不織布とを2液型ポリエステル系樹脂を用い、非接合面積率が52%の斜め格子柄グラビア版で、多孔質フィルム面に接着剤を途布して、ドライラミネート法で貼り合わせ、通気性積層体を得た。さらに、得られた通気性積層体を用いてカイロを作製し、その評価を行なった。表2に通気性積層体およびカイロの特性を示す。表2から、非接合面積率を多くしても、使い捨てカイロとしての通気性が低く、最高温度、安定温度が低く、カイロの適正外の特性となったことが分かる。
[Comparative Example 1]
Linear low density polyethylene of metallocene catalyst (Dow Chemical Co., density 0.915, MFR (190 ° C.) 3.5 g / 10 min) 62 wt%, high density low density polyethylene 5 wt%, calcium carbonate (D = 50 %, 4 μm) A porous film was obtained in the same manner as in Example 1 except that a mixed resin consisting of 32 wt%, stearic acid and antioxidant in total 1 wt% was melt kneaded at 220 ° C. to obtain a mixed raw material. . The properties of the obtained porous film are shown in Table 1.
Next, the obtained porous film and the nonwoven fabric described in Example 1 were used in a two-part polyester resin, and an oblique lattice pattern gravure plate having a non-bonded area ratio of 52%, and an adhesive was applied to the porous film surface. It spread and bonded together by the dry lamination method, and the air permeable laminated body was obtained. Furthermore, a warmer was produced using the obtained air-permeable laminate and evaluated. Table 2 shows the characteristics of the breathable laminate and the body warmer. From Table 2, it can be seen that even if the non-bonded area ratio is increased, the air permeability as a disposable warmer is low, the maximum temperature and the stable temperature are low, and the characteristics are not appropriate for the warmer.
[比較例2]
メタロセン触媒の直鎖状低密度ポリエチレン(ダウケミカル社製、密度0.915、MFR(190℃)3.5g/10分)41wt%、高圧法の低密度ポリエチレン5wt%、炭酸カルシウム(D=50%、4μm)53wt%、ステアリン酸および酸化防止剤が合計で1wt%からなる混合樹脂を220℃で溶融混練し、混合原料とした以外は実施例1と同様の方法で多孔質フィルムを得た。得られた多孔質フィルムの特性を表1に示す。
次いで、得られた多孔質フィルムと実施例1に記載の不織布とを2液型ポリエステル系樹脂を用い、グラビア方式で多孔質フィルム面に接着剤を途布して、非接合面積率が19%の斜め格子柄グラビア版で、多孔質フィルム面に接着剤を途布して、ドライラミネート法で貼り合わせ、通気性積層体を得た。さらに、得られた通気性積層体を用いてカイロを作製し、その評価を行なった。表2に通気性積層体およびカイロの特性を示す。表1および表2から、多孔質フィルムの開孔が多くなり、エッジ切れやすいものとなり、使い捨てカイロの製袋加工適正が得られなかったことが分かる。
[Comparative Example 2]
Linear low density polyethylene of metallocene catalyst (Dow Chemical Co., density 0.915, MFR (190 ° C.) 3.5 g / 10 min) 41 wt%, high density low density polyethylene 5 wt%, calcium carbonate (D = 50 %, 4 μm) A porous film was obtained in the same manner as in Example 1 except that a mixed resin consisting of 53 wt% and stearic acid and an antioxidant totaling 1 wt% was melt kneaded at 220 ° C. to obtain a mixed raw material. . The properties of the obtained porous film are shown in Table 1.
Subsequently, the obtained porous film and the nonwoven fabric described in Example 1 were used with a two-component polyester resin, an adhesive was distributed on the porous film surface by a gravure method, and the non-bonded area ratio was 19%. With an oblique lattice pattern gravure plate, an adhesive was spread on the surface of the porous film and bonded by a dry laminating method to obtain a breathable laminate. Furthermore, a warmer was produced using the obtained air-permeable laminate and evaluated. Table 2 shows the characteristics of the breathable laminate and the body warmer. From Tables 1 and 2, it can be seen that the pores of the porous film are increased and the edges are easily cut off, and the bag making process suitability of the disposable body warmer cannot be obtained.
[比較例3]
高圧法の低密度ポリエチレン添加しない樹脂配合であること、および、未延伸フィルムを延伸倍率5.5倍で延伸加工したこと以外は実施例5と同様に行って多孔質フィルムを得、次いで得られた多孔質フィルムを用いて実施例5と同様に通気性積層体および使い捨てカイロを得た。表1および表2に多孔質フィルム、通気性積層体およびカイロの特性を示す。多孔質フィルムとしては、延伸加工時において無機充填剤の脱落が多く、製袋加工時にはエッジ切れが多く発生し、得られた使い捨てカイロは最高温度がより高く、膨らみが生じるなど問題があった。
[Comparative Example 3]
A porous film was obtained in the same manner as in Example 5 except that the resin composition was not added with low-density polyethylene in the high-pressure method and that the unstretched film was stretched at a stretch ratio of 5.5. Using the porous film, a breathable laminate and a disposable body warmer were obtained in the same manner as in Example 5. Tables 1 and 2 show the characteristics of the porous film, the air-permeable laminate, and the body warmer. As for the porous film, there are many problems such that the inorganic filler is often dropped during the stretching process, the edge breakage occurs frequently during the bag making process, and the obtained disposable warmer has a higher maximum temperature and bulges.
本発明の通気性積層体は、使い捨てカイロの袋体構成部材に使用した際に、熱シール性が良く、発熱最高温度および発熱持続時間などの使い捨てカイロの製品特性に優れ、且つ熱シール時のエッジ切れなどが少なく生産性に優れており、使い捨てカイロの袋体構成部材として有用である。 The breathable laminate of the present invention has good heat sealability when used as a bag component of a disposable body warmer, is excellent in the product characteristics of the disposable body warmer such as the maximum heat generation temperature and the heat generation duration time, and when heat sealed. There are few edge breaks etc. and it is excellent in productivity, and it is useful as a bag body structural member of a disposable body warmer.
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