JPS631540A - Packaging material for photosensitive material - Google Patents
Packaging material for photosensitive materialInfo
- Publication number
- JPS631540A JPS631540A JP61144758A JP14475886A JPS631540A JP S631540 A JPS631540 A JP S631540A JP 61144758 A JP61144758 A JP 61144758A JP 14475886 A JP14475886 A JP 14475886A JP S631540 A JPS631540 A JP S631540A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- layer
- film
- properties
- light
- 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.)
- Granted
Links
- 239000000463 material Substances 0.000 title claims description 51
- 239000005022 packaging material Substances 0.000 title claims description 33
- 239000010410 layer Substances 0.000 claims description 115
- 229920005989 resin Polymers 0.000 claims description 81
- 239000011347 resin Substances 0.000 claims description 81
- 230000003068 static effect Effects 0.000 claims description 18
- 229920005992 thermoplastic resin Polymers 0.000 claims description 18
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 13
- 239000005977 Ethylene Substances 0.000 claims description 13
- 239000000853 adhesive Substances 0.000 claims description 13
- 230000001070 adhesive effect Effects 0.000 claims description 13
- 239000000314 lubricant Substances 0.000 claims description 13
- 239000004711 α-olefin Substances 0.000 claims description 13
- 239000006229 carbon black Substances 0.000 claims description 10
- 229920006026 co-polymeric resin Polymers 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 7
- 229920000092 linear low density polyethylene Polymers 0.000 claims description 5
- 239000004707 linear low-density polyethylene Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 229920013716 polyethylene resin Polymers 0.000 claims description 4
- 239000012793 heat-sealing layer Substances 0.000 claims description 2
- 229920001038 ethylene copolymer Polymers 0.000 claims 1
- 239000010408 film Substances 0.000 description 60
- 238000000034 method Methods 0.000 description 55
- 239000000047 product Substances 0.000 description 32
- 238000007789 sealing Methods 0.000 description 31
- 229920001684 low density polyethylene Polymers 0.000 description 28
- 239000004702 low-density polyethylene Substances 0.000 description 27
- 230000008569 process Effects 0.000 description 26
- 239000000126 substance Substances 0.000 description 20
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 17
- 229910052751 metal Inorganic materials 0.000 description 14
- 239000002184 metal Substances 0.000 description 14
- 229910052782 aluminium Inorganic materials 0.000 description 13
- 239000000843 powder Substances 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 11
- -1 Polyethylene Polymers 0.000 description 9
- 235000019241 carbon black Nutrition 0.000 description 9
- 229920005672 polyolefin resin Polymers 0.000 description 8
- 239000004698 Polyethylene Substances 0.000 description 7
- 239000002131 composite material Substances 0.000 description 7
- 239000003925 fat Substances 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 239000012790 adhesive layer Substances 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 239000011888 foil Substances 0.000 description 6
- 238000010030 laminating Methods 0.000 description 6
- 238000003475 lamination Methods 0.000 description 6
- 238000004806 packaging method and process Methods 0.000 description 6
- 239000002216 antistatic agent Substances 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 230000005611 electricity Effects 0.000 description 5
- 239000011342 resin composition Substances 0.000 description 5
- 239000002356 single layer Substances 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 4
- 238000005299 abrasion Methods 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000903 blocking effect Effects 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 229920001903 high density polyethylene Polymers 0.000 description 4
- 239000004700 high-density polyethylene Substances 0.000 description 4
- 239000005001 laminate film Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 3
- 239000004594 Masterbatch (MB) Substances 0.000 description 3
- 230000032798 delamination Effects 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 238000003780 insertion Methods 0.000 description 3
- 230000037431 insertion Effects 0.000 description 3
- 229920000554 ionomer Polymers 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000012858 packaging process Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 241000282320 Panthera leo Species 0.000 description 2
- 241000872198 Serjania polyphylla Species 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000011231 conductive filler Substances 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- CGPRUXZTHGTMKW-UHFFFAOYSA-N ethene;ethyl prop-2-enoate Chemical compound C=C.CCOC(=O)C=C CGPRUXZTHGTMKW-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000012847 fine chemical Substances 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 229920001748 polybutylene Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- AFUDNVRZGPHSQO-UHFFFAOYSA-N 2-(2-methylpropylamino)-1,2-diphenylethanol Chemical compound C=1C=CC=CC=1C(NCC(C)C)C(O)C1=CC=CC=C1 AFUDNVRZGPHSQO-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- HKOZMNXUDWJMQE-UHFFFAOYSA-N 3-(2-ethenylphenyl)prop-2-enenitrile Chemical compound C=CC1=CC=CC=C1C=CC#N HKOZMNXUDWJMQE-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
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 241001330002 Bambuseae Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 1
- YQEZLKZALYSWHR-UHFFFAOYSA-N Ketamine Chemical compound C=1C=CC=C(Cl)C=1C1(NC)CCCCC1=O YQEZLKZALYSWHR-UHFFFAOYSA-N 0.000 description 1
- 229920000339 Marlex Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229920003182 Surlyn® Polymers 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000002998 adhesive polymer Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 238000000498 ball milling Methods 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000010382 chemical cross-linking Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 229920003020 cross-linked polyethylene Polymers 0.000 description 1
- 239000004703 cross-linked polyethylene Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 238000009820 dry lamination Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 239000004715 ethylene vinyl alcohol Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- RZXDTJIXPSCHCI-UHFFFAOYSA-N hexa-1,5-diene-2,5-diol Chemical compound OC(=C)CCC(O)=C RZXDTJIXPSCHCI-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000002715 modification method Methods 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000003348 petrochemical agent Substances 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920005670 poly(ethylene-vinyl chloride) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Wrappers (AREA)
- Laminated Bodies (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は写真感光材料に適した包装材料に関するもので
ある。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a packaging material suitable for photographic materials.
写真感光材料用包装材料は種々のタイプのものが広く実
用化されており、その使途に従って様々の性能が要求さ
れている。Various types of packaging materials for photographic materials have been widely put into practical use, and various performances are required depending on the intended use.
光に曝するとその品質価値を失なう写真感光材料用包装
材料としては光を完全に遮断する包装材料が使用される
。この場合、要求される特性としては包装材料スリット
適性、ガスバリャ性、遮光性、防湿性、剛住、物理強度
(破断強度、引裂強度、衝撃穴あけ強友、rルゴテスト
強反、摩耗強度等)、ヒートシール適注(ヒートシール
強度、カットシール性、ホットタック性、夾難物シール
性等)、経時ヒートシール強度、帯電防止性、平面性、
すべり特性などが挙げられる。これらの諸性質を単一の
フィルム材料で兼ねそなえることは非常に困難であり、
従来、一般には第5図に示すようなカーデンブラックや
顔料等を練り込んだ非常に厚手の高圧法分岐状低密度ポ
リエチレン(以後LDPEと表示)樹脂遮光フイルム層
8aの単一層フィルムやLDPE #脂フイルムと紙、
アルミニウム消、セロハン等のフレキシブルシ一ト層と
の複合ラミネートフィルムなどが使用されてきた。複合
ラミネートフィルムの例を第6図に示すが、このものは
防湿性と物理強度を特に要求されるロール状カラー印画
紙製品に使用されているもので、LDPE樹脂遮光フィ
ルム48mに接着層5を介してアルミニウム箔層9を積
層し、さらに接着層5を介してフレキシブルシ一ト層6
を積層し、さらにその上に接着層5を介してLDPE樹
脂遮光フィルム層8&を積層したものである。Packaging materials that completely block light are used as packaging materials for photographic materials that lose their quality value when exposed to light. In this case, the required properties include packaging material slit suitability, gas barrier properties, light shielding properties, moisture proofing properties, rigidity, physical strength (breaking strength, tear strength, impact perforation strength, R Lugo test strength, abrasion strength, etc.), Heat sealing properties (heat sealing strength, cut sealing properties, hot tack properties, impurities sealing properties, etc.), heat sealing strength over time, antistatic properties, flatness,
Examples include slip characteristics. It is extremely difficult to have all of these properties in a single film material.
Conventionally, a very thick high-pressure branched low-density polyethylene (hereinafter referred to as LDPE) resin light-shielding film layer 8a or a single layer film of a very thick high-pressure branched low-density polyethylene (hereinafter referred to as LDPE) resin light-shielding film layer 8a kneaded with carden black, pigments, etc. as shown in FIG. film and paper,
Composite laminate films with flexible sheet layers such as aluminum foil and cellophane have been used. An example of a composite laminate film is shown in Fig. 6, which is used in rolled color photographic paper products that particularly require moisture resistance and physical strength. An aluminum foil layer 9 is laminated through the adhesive layer 5, and a flexible sheet layer 6 is laminated through the adhesive layer 5.
LDPE resin light-shielding film layer 8& is further laminated thereon via an adhesive layer 5.
本発明者は、感光物質用包装材料を改良すべく鋭意研究
を行ない、2層の一軸延伸フィルムを組み合わせること
によって物理強度を向上させたもの(%開昭57−67
54号公報)を既に開示している。また、シート状の発
泡体の両面に一軸分子配向熱可盟性樹脂フィルムを積層
してなる積層フィルムにおいて、シート状発泡体の厚さ
を0.3〜2.0ms、発泡倍率を5〜50倍にし、二
層のー軸分子配向フイルムを分子配向軸が30度以上の
角度で交差する様に発泡体の両面に接着した積Nフィル
ムを既に開示した。(特開昭59−201848号公報
)
〔発明が解決しようとする問題点〕
従来の複合ラミネートフィルムは前述の物理特性を向上
させるべく構成されたものである。しかし、防湿と帯電
防止のためアルミニウム箔を使用しているので重量裂品
やエッジがシャープなロールフィルム製品等では物理特
性は十分とはいえず、包装作業中に裂けたり穴があいた
り、ヒートシール部がはがれるなどの欠点があった。さ
らにカーざンブラック等の遮光性物質を大量に添加する
と物理強度の劣化やヒートシール性の悪化が太きくなり
、添加量は3重量チ前後、トータルフィルム厚さは70
μm以上とする必要があった。このため、包装はカサば
り積層体フィルムの剛度が大きくなり包装作業性が悪化
し且つコスト的にも高価なものとなクていた。The present inventor has conducted extensive research to improve packaging materials for photosensitive materials, and has developed a material with improved physical strength by combining two layers of uniaxially stretched film (%
No. 54) has already been disclosed. In addition, in a laminated film formed by laminating uniaxial molecularly oriented thermoplastic resin films on both sides of a sheet-like foam, the thickness of the sheet-like foam is 0.3 to 2.0 ms, and the expansion ratio is 5 to 50. A laminated N film has already been disclosed in which two layers of -axis molecularly oriented films are adhered to both sides of a foam such that the molecular orientation axes intersect at an angle of 30 degrees or more. (Japanese Unexamined Patent Publication No. 59-201848) [Problems to be Solved by the Invention] Conventional composite laminate films are constructed to improve the above-mentioned physical properties. However, since aluminum foil is used to prevent moisture and static electricity, the physical properties of heavy products and roll film products with sharp edges cannot be said to be sufficient. There were drawbacks such as the seal part peeling off. Furthermore, if a large amount of light-shielding substances such as Carzan Black are added, the physical strength and heat sealability will deteriorate significantly.
It was necessary to make it more than μm. As a result, the packaging becomes bulky and the rigidity of the laminate film increases, resulting in poor packaging workability and high costs.
例えばロール状カラー印画紙の包装に使用されていた第
6図に示す7層構成の積層フィルムでも、防湿と帯電防
止のためアルミニウム箔を使用しているので引裂き強度
や衝撃穴アケ強度、rルゴテスト強度等が不足している
。特開昭59−201848号公報記載の包装材料は引
張強度、グルデテスト強匿、衝撃穴アケ強度等の物理強
度を改善している。For example, even in the seven-layer laminated film shown in Figure 6, which was used to package rolls of color photographic paper, aluminum foil is used to prevent moisture and static electricity. Strength etc. is insufficient. The packaging material described in JP-A-59-201848 has improved physical strengths such as tensile strength, Gourdet test strength, and impact hole damage strength.
しかしこの積層フィルムは厚さが大きく高遮光写真感光
材料用としては帯電防止が不十分な上遮光性や防湿性等
を確保するためのヒートシール適性が悪くさらに自動製
袋適性がなく、ヒートシール面に耐熱フィルムをはさみ
特殊な冷却装置を用いたヒートシーラーで製袋した袋に
製品を挿入、密封包装するため非常に高価な包装となっ
ていた。However, this laminated film is too thick and has insufficient antistatic properties for use in highly light-shielding photosensitive materials, and is not suitable for heat-sealing to ensure light-shielding and moisture-proof properties.Furthermore, it is not suitable for automatic bag making, and is not suitable for heat-sealing. The packaging was extremely expensive because the product was inserted into a bag made with a heat sealer using a special cooling device and a heat-resistant film sandwiched between the sides and then sealed.
本発明は、以上の問題点を改善し、製品挿入性、経時ヒ
−トシール強度、物理強肛、ヒートシール適性、帯電防
止性等の向上を図った安価な写真感光材料用包装材料を
提供することを目的とする。The present invention solves the above-mentioned problems and provides an inexpensive packaging material for photographic materials that improves product insertability, heat-sealing strength over time, physical strength, heat-sealing suitability, antistatic property, etc. The purpose is to
本発明は上記目的を達成するために、
エチレンとα−オレフィンとの共重合体であろ直鎖状低
密度?リエチレン樹脂が30〜99.49重量チ、カー
?ンブラックが0,5〜10重量チそして滑剤が0.0
1〜1.00重量係のヒートシール層であって静摩擦係
数が0.12〜0.37である内層と、熱可塑性樹脂で
形成された中間層と、熱可塑性樹脂で形成され静摩擦係
数が内層より0。05以上大きくかつその絶対値が0.
19以上である外層とから成り、該内層と中間層及び外
層と中間層の接着強度が109/i5m巾以上である同
時多層共押し出し遮光フィルムを具備していることを特
徴とする写真感光材料用包装材料
を構成したものである。In order to achieve the above object, the present invention uses a copolymer of ethylene and α-olefin or a linear low density one. Liethylene resin weighs 30 to 99.49 kg, car? Black is 0.5-10% by weight and lubricant is 0.0
an inner layer that is a heat-sealing layer with a weight coefficient of 1 to 1.00 and a coefficient of static friction of 0.12 to 0.37, an intermediate layer made of a thermoplastic resin, and an inner layer made of a thermoplastic resin and a coefficient of static friction of 0.12 to 0.37. 0.05 or more and its absolute value is 0.05 or more.
19 or more, and a simultaneous multilayer coextruded light-shielding film having an adhesive strength of 109/i5m or more between the inner layer and the intermediate layer and between the outer layer and the intermediate layer. It is made up of packaging materials.
本発明の内層に必須のエチレンとα−オレフィンとの共
重合体である直鎖状低密度ポリエチレン樹脂は、一般に
はL−LDPE樹脂( L1near LovrDen
sity Polyetylane即ち直鎖状低密度ポ
リエチレンの頭文字の略号)と呼ばれる直鎖状低密度?
リエチレン樹脂である。重合プロセスとしては中低圧装
置を用いる気相法、液相法(溶液法)と高圧改良装置を
用いろ高圧改造法等がある。特に低圧法のL−LDPE
樹脂が低コストなので好ましい。The linear low density polyethylene resin which is a copolymer of ethylene and α-olefin which is essential for the inner layer of the present invention is generally L-LDPE resin (L1near LovrDen
Linear low density polyethylene (abbreviation for linear low density polyethylene)
It is polyethylene resin. Polymerization processes include a gas phase method using medium and low pressure equipment, a liquid phase method (solution method), and a high pressure modification method using a high pressure modification equipment. Especially low pressure L-LDPE
Resins are preferred because of their low cost.
具体例を藺品名で示せば、ユニポールとrUFLIN(
UCC社)、ダウレックス(ダウケミカル社)、スク
レアー(デュポンカナダ社)、マーレックス(フィリッ
プス社)、ネオゼックスとウルトゼ,クス(三井石油化
学)、日石リニレックス(日本石油化字)、出光ポリエ
チレンーL(出光石油化学)、スタミレックス( DS
M社)、N′UCポリエチレンーLL (日本二二カー
)などが挙げられる。αーオレフィンとしてはブテンー
1、オクテン−1、ヘキセン−1、4−メチルベンテン
−1、ヘプテン−1などが使用され、その量はポリマー
の0. 5〜15モルチ程度である。密度は、一般に低
、中密度程度とされているが、市販品では0.87〜0
. 9 4 fJ/CM”の範囲内にあるものが多い。Specific examples are Unipol and rUFLIN (
UCC), Dowlex (Dow Chemical), Sclar (DuPont Canada), Marlex (Philips), Neozex and Ultose, Kusu (Mitsui Petrochemical), Nippon Linirex (Nippon Petrochemical), Idemitsu Polyethylene L (Idemitsu Petrochemical), Stamilex (DS
(Company M), N'UC Polyethylene-LL (Nippon 22 Car), etc. As the α-olefin, 1-butene, 1-octene, 1-hexene, 4-methylbentene-1, heptene-1, etc. are used, and the amount thereof is 0.1% of the polymer. It is about 5 to 15 molti. The density is generally considered to be low to medium density, but commercially available products have a density of 0.87 to 0.
.. Many of them are within the range of 94 fJ/CM.
これらのL−LDI’E樹脂の中で、コストと物理強度
とヒートシール強度の点から特に好ましいのは、エチレ
ン含有量が90〜99.5モルチ、αオレ7インt 有
itが0. 5〜lOモルチ、メルトインデックス(以
後Mlと表示)が0.4〜30g/1o分(ASTM
D−1238)密度が0.8 7 0〜0.9 4 0
FCrn3(ASTM D−1505)、αオレフィ
ンの炭素数が6〜8ヶの低圧法の液相法プロセスと気相
法プロセスによるL−LDPE 文脂である。最も好ま
しい代表的な商品名をあげると、エチレンにαオレフィ
ン側鎖として炭素数6ヶの4メチルペンテン−1を用い
たL−LDPE tH脂と1−ては三井石油化学(沫)
のネオゼックスとウルトゼックスがあり、αオレ7イン
側鎖として炭素数8ヶのオクテン−1を用いたL−LD
PE樹脂としてはDSM社のスタミレックスとダウケミ
カル社のダウレックス等がある。(以上3社品共、低圧
法の液相法プロセスによるL−LDPE函脂である。)
低圧法の気相法プロセス品としてはαオレフィン側鎖と
してヘキセンー1を用いたUCCの!IN等がある。Among these L-LDI'E resins, those having an ethylene content of 90 to 99.5 molt and an α ole 7 int of 0.05 are particularly preferred from the viewpoint of cost, physical strength, and heat seal strength. 5-10 molti, melt index (hereinafter referred to as Ml) is 0.4-30 g/10 min (ASTM
D-1238) Density is 0.8 7 0 to 0.9 4 0
FCrn3 (ASTM D-1505), L-LDPE bunsou produced by a low-pressure liquid phase process and a gas phase process in which the alpha olefin has 6 to 8 carbon atoms. The most preferred representative product name is L-LDPE, which uses 4-methylpentene-1 with 6 carbon atoms as the α-olefin side chain in ethylene.
There are Neozex and Urtozex, and L-LD uses octene-1 with 8 carbon atoms as the α-ole7yne side chain.
Examples of PE resins include Stamilex from DSM and Dowlex from Dow Chemical. (All of the above three companies' products are L-LDPE case resin produced by the low-pressure liquid phase process.)
As a low-pressure gas phase process product, UCC using hexene-1 as the α-olefin side chain! There are IN etc.
L−LDPK樹脂は単独でも他の各種熱可塑性樹脂や各
種添加剤と混合して用いられてもよい。特に物理強度(
引裂き強度や衝撃穴アケ強度等)やヒートシール性(シ
ール強度、ホットタック性、夾雑物シール性等の確保)
等他の樹脂を用いた場合よりすぐれた特性を確保するに
は少くともL−LDPE樹脂を30重量チ含む樹脂組成
とするのが必須である。L−LDPE 71{脂は、異
なったα−オレフィンを有する2種以上のL−LDPE
@脂の混合組成でも良いのは言うまでもない。L-LDPK resin may be used alone or in combination with other various thermoplastic resins and various additives. Especially physical strength (
(tear strength, impact hole resistance, etc.) and heat sealability (ensuring sealing strength, hot tack performance, contaminant sealing performance, etc.)
In order to ensure better properties than when other resins are used, it is essential to have a resin composition containing at least 30 parts by weight of L-LDPE resin. L-LDPE 71 {fat is two or more types of L-LDPE having different α-olefins
It goes without saying that a mixed composition of @fat may also be used.
L−LDPE樹脂と混合してインフレーシ偽ンフィルム
成形性を改善し、物理特性をあまり低下させない樹脂と
してはポリオレフィン系樹脂詩にLDPK樹脂、EvA
樹脂(エチレン・酢酸ビニル共重合体函脂)、EEA樹
脂(エチレン・アクリル酸エチル共重合体樹脂)が好ま
しい。Among the resins that can be mixed with L-LDPE resin to improve the formability of blown film without significantly reducing physical properties are polyolefin resins, LDPK resin, and EvA.
Resin (ethylene/vinyl acetate copolymer resin) and EEA resin (ethylene/ethyl acrylate copolymer resin) are preferred.
内層K必須のカーゴンブラックは、経時ヒートシール強
度維持、遮光性、帯電防止性等を施すためのものであり
、その添加量は0.5〜10重量%である。この添加量
はフィルムの物理強度、フィルム成形性、防湿性、帯電
防止性、フィルム品質の点から限定される。0. 5重
量チ未満では遮光性経時ヒートシール強度維持帯電防止
性が満足できず、10重量チをこすと吸湿性が大きくな
りフィルム成形性が悪化するだり゛で物理強度やヒート
シール性防湿性等の特性が問題Kなる。又写真感光材料
とのこすれに.より摩耗して黒色の粉が多発し、感光材
料に班点状の故障を生じる原因となる。カーボンプラッ
クだけで表面抵抗値を1010Ω以下にするためには導
電性カーボンプラックを添加する必要がある。Cargon black, which is essential in the inner layer K, is used to maintain heat seal strength over time, provide light shielding properties, antistatic properties, etc., and the amount added is 0.5 to 10% by weight. The amount added is limited in terms of the physical strength of the film, film formability, moisture resistance, antistatic property, and film quality. 0. If the weight is less than 5 weight, the light shielding properties, heat sealing strength over time, and antistatic properties will not be satisfied, and if the weight is 10 weight, the hygroscopicity will increase and the film formability will deteriorate. Characteristics are the problem. Also, due to rubbing with photographic materials. As a result of further abrasion, black powder is produced frequently, causing speckle-like failures in the photosensitive material. In order to reduce the surface resistance to 1010Ω or less using carbon plaque alone, it is necessary to add conductive carbon plaque.
導電性カーポンプラックの代表例としてはアセチレンカ
ーボンブラックや変性副生カーゲンブラックであるケッ
チェンカーゴンブラック等がある。各種の導電性物質と
各種のカーボンブラックとブレンドして帯電防止効果を
向上させることも好ましい。Typical examples of conductive carpon black include acetylene carbon black and Ketjen Cargon Black, which is a modified by-product cargen black. It is also preferable to improve the antistatic effect by blending various conductive substances with various carbon blacks.
例えば各種の金属導電性粒子や各種の帯電防止剤{丸茂
秀雄著゛帯電防止剤″(辛書房)に詳細に記載されてい
る。}や金属粉末、峨維状導電性フィラー又は導電性フ
ィラーを液状ポリマー及び/又は溶剤可溶ポリマーでか
ためた物等公知の導電性物質とカーゲンブラックとをブ
レンドすることも好ましい。本発明にはカーボンプラッ
クの中でもP}{5〜9、平均粒子径10〜120mμ
のものが好ましく、特にPl{6〜8、平均粒子径15
〜30mμのオイルファーネスカーボンブラックが分散
性、遮光性確保の点で好ましい。特K写真感光材料用包
装材料としてこのような声及び粒子径のものを使用する
ことによって、カブリの発生が少ない、感光度の増減の
発生が少ない、遮光能力が大きい、写真感光材料に悪影
響を与えず、熱可凰性樹脂フィルムに添加した場合でも
カーデンブラックの塊(ブッ)やフィッシュアイ等のビ
ンホールが発生しにくい等の数々の利点を有する包装材
料を得ることができる。For example, various metal conductive particles, various antistatic agents (described in detail in "Antistatic Agents" by Hideo Marumo (Shin Shobo)), metal powders, fibrous conductive fillers, or conductive fillers. It is also preferable to blend Cargen Black with a known conductive substance such as one hardened with a liquid polymer and/or a solvent-soluble polymer. 10~120mμ
Those with Pl{6 to 8, average particle size 15 are preferable, and in particular
Oil furnace carbon black of ~30 mμ is preferable from the viewpoint of ensuring dispersibility and light-shielding properties. By using materials with such characteristics and particle sizes as packaging materials for special K photographic light-sensitive materials, there will be little fog, little increase or decrease in photosensitivity, high light-shielding ability, and no negative effects on the photographic light-sensitive materials. Even when it is added to a thermoplastic resin film without adding it, it is possible to obtain a packaging material that has a number of advantages, such as being less likely to generate clumps of carden black or bottle holes such as fish eyes.
カー?ンブラックをL−LDPE樹脂に配合する使用形
態としては粉末添加法、ペースト状添加法、潤性添加法
、顆粒状添加法、コン・!ウンド法、マスターパッチ法
等種々あるが、マスターパッチ法がコスト、作業機の汚
染防止等の点で好ましい。car? Forms of use for blending black with L-LDPE resin include powder addition method, paste addition method, moisturizing addition method, granule addition method, and con-! Although there are various methods such as the wind method and the master patch method, the master patch method is preferable in terms of cost and prevention of contamination of working equipment.
公知文献の特公昭40−26196号公報には有機溶媒
に溶解した重合体の溶液中Kカーゴンプ ゛ラックを分
散せしめて、重合体力−ボンプラックのマスターバッチ
をつくる方法を、特公昭43−10362号公報にはカ
ーデンブラックをIリエチレンに分散してマスターパッ
チをつくる方法が示されている。Japanese Patent Publication No. 40-26196, which is a publicly known document, describes a method for preparing a masterbatch of polymer carbon plack by dispersing K cargon plac in a solution of a polymer dissolved in an organic solvent, and Japanese Patent Publication No. 10362/1982 describes a method for preparing a masterbatch of polymer carbon plac. describes a method for preparing a master patch by dispersing carden black in I-lyethylene.
マスターパッチ方法の場合Kは、まずポリオレ7イン樹
脂(好まし< &’!. LDPE . L−L.)P
B , EVA ,EEA . EMA等)に10重量
チ以上、一般には30重i%以上の高密度にカー〆ンブ
ラックを混合してマスターパッチを作る。そして、最終
的に内層中のカーがンブラック量が0. 5〜10重世
係になる様にこのマスターバッチ4レットを計量し、L
−LDPE樹脂又はL−LDPEm脂に添化する熱可塑
性樹脂と混合する。In the case of the master patch method, K is first made of polyolefin resin (preferably <&'!. LDPE. L-L.) P
B, EVA, EEA. A master patch is made by mixing carbon black (e.g. EMA, etc.) at a high density of 10% by weight or more, generally 30% by weight or more. Finally, the amount of carbon black in the inner layer is 0. Weigh out 4 lets of this masterbatch so that it will weigh 5 to 10 times, and
- Mix with a thermoplastic resin to be added to the LDPE resin or L-LDPEm resin.
内層に必須の滑剤は、写真感光材料に悪影響を与えず、
製品挿入適性、ブロッキング防止、フィルム成形性、ハ
クリ帯電防止性等を良くするためのものである。この滑
剤の添加量は静電気防止、製品挿入適性、フィルム成形
性、プロッキング防止、及び添加量が多すぎる場合の写
真感光材料等へのbresdoutによろべと付き発生
、ごみ付着等が発生しないようにするため0.01〜1
. 0重量チである。The lubricant, which is essential for the inner layer, does not have a negative effect on the photographic material.
This is to improve product insertion suitability, blocking prevention, film formability, anti-static properties when peeling off, etc. The amount of this lubricant added is determined to prevent static electricity, suitability for product insertion, film formability, prevention of blocking, and to prevent the occurrence of stickiness, dust adhesion, etc. due to bresdout on photographic materials if the amount added is too large. 0.01 to 1 to
.. It is 0 weight.
写真感光材料K悪影響を与えない市販の代表的滑剤名と
製造メーカー名を以下に記載するが本発明はこれらに限
定されるものではない。The names of typical commercially available lubricants and manufacturers that do not adversely affect photographic light-sensitive materials are listed below, but the present invention is not limited thereto.
(1)シリコン系滑剤;各種グレードのジメチルポリシ
ロキサン(信越シリコーン,東
レシリコーン等)
(2)オレイン酸アミド系滑剤:アーモスリップCP(
ライオン,アクゾ).ニュートロン
(日本鞘化),ニュートロン
E−18 (日本精化),アマイドO
(日東化学),アル7口E−10
(日本油脂),ダイヤミッド
0−200 (日本化成),ダイヤミ
ッドG−200 (日本化成)等
(3)エルカ酸アミド系滑剤;アルンローP−10 (
日本油脂)等
(4)ステアリン酸アミド系滑剤;アルフローS−10
(日本油脂),ニュートロン2(日本
精化),ダイヤミッド200(日
本化成)等
(5)ビス脂肪酸アミド系滑剤 ;ピスアマイド(日本
化成),ダイヤミッド200ビス
(日本化成),アーモワックス
DBS (ライオンアクゾ)等
(6)アルキルアミン系滑剤;エレクトロストリッパー
TS−2等がある。(1) Silicone lubricant; various grades of dimethylpolysiloxane (Shin-Etsu Silicone, Toray Silicone, etc.) (2) Oleic acid amide lubricant: Armoslip CP (
Lion, Akzo). Neutron (Nippon Sheath Chemical), Neutron E-18 (Nippon Fine Chemical), Amide O (Nitto Chemical), Al7kuchi E-10 (Nippon Oil & Fats), Diamid 0-200 (Nippon Kasei), Diamid G -200 (Nippon Kasei) etc. (3) Erucic acid amide lubricant; Arunro P-10 (
(4) Stearic acid amide lubricant; Alflo S-10
(NOF), Neutron 2 (Nippon Fine Chemicals), Diamid 200 (Nippon Kasei), etc. (5) Bis fatty acid amide lubricants; Pisamide (Nippon Kasei), Diamid 200 Bis (Nippon Kasei), Armowax DBS ( (6) Alkylamine lubricants; Electro Stripper TS-2, etc.
また、内層は静摩擦係数が0.12〜0.37である。Further, the inner layer has a static friction coefficient of 0.12 to 0.37.
この静摩擦係数は、テストすべきシートの1部を切取り
、これを縦75酎横35mの荷fi 200gのブロッ
クの底面に貼着する。一方、テストすべきシートの1部
を同様に切取って傾斜面に貼着lj 、前記ブロックの
・,・一ト面を傾斜面上に載せ、この傾斜面の傾斜角度
を変化させて、前記ブロックが滑り始めた角度θを読み
取った後tanθとして求めた値である。This coefficient of static friction was determined by cutting out a part of the sheet to be tested and pasting it on the bottom of a block measuring 75 m long and 35 m wide and weighing 200 g. On the other hand, a part of the sheet to be tested is similarly cut out and pasted on an inclined surface, one side of the block is placed on the inclined surface, the inclination angle of this inclined surface is changed, and the This is the value obtained as tanθ after reading the angle θ at which the block started to slide.
靜J$擦係数が0.12未満では写真感光材料が輸送中
に袋の中で動きすぎてスリキズや摩擦力ブリを発生させ
るだけでなく、フィルム成形後の巻取りや積層工程の巻
取り時にすべりすぎて巻き取れなかったり、たけのこ状
に巻姿がなり実用化困難である。If the friction coefficient is less than 0.12, the photographic material will not only move too much in the bag during transportation, causing scratches and frictional brittleness, but will also cause damage during winding after film forming or during the lamination process. It is difficult to put it into practical use because it is too slippery and cannot be rolled up, or it takes on a bamboo shoot shape.
又静摩擦係数が0.37をこえると厚真感光材料の包装
工程で袋に入りに<<、むりして入れようとすると袋が
破れたり、写真感光材料にスリキズや摩擦力ブリを発生
させる。袋の場合は、且つプロッキングしやすくなり、
内層と内層がプロ,キングするだけでなく内層と写真感
光材料が接着し使用不可にすることがある。又輸送工程
中に写真感光材料とのこすれにより摩耗し黒粉が多発し
、この黒粉が写真感光材料の感光層に班点状に付着した
故障が起る。Furthermore, if the static friction coefficient exceeds 0.37, the bag may be torn if the photosensitive material is squeezed into the bag during the packaging process, and the photosensitive material may be scratched or have friction brittleness. In the case of bags, it is easier to block,
Not only can the inner layer be damaged, but the inner layer and the photosensitive material may adhere to each other, making it unusable. In addition, during the transportation process, the photosensitive material is abraded due to rubbing against the photosensitive material, producing a large amount of black powder, and this black powder adheres to the photosensitive layer of the photosensitive material in the form of speckles, resulting in failure.
中間層は、熱可辺性樹脂が単独又は2橿以上混合して形
成されている。この熱可塑性樹脂は内層及び外層との接
着力が10’l/15■巾以上となるような樹脂組成に
して用いられる。内層のL−LDPE樹脂との接着強度
確保、フィルム成形性、カール減少、汎用樹脂で安価等
のため、下記のポリオレフィン樹脂が好ましい。The intermediate layer is formed of a single thermoplastic resin or a mixture of two or more thermoplastic resins. This thermoplastic resin is used in such a resin composition that the adhesive force between the inner layer and the outer layer is 10'l/15cm or more. The following polyolefin resins are preferred because they ensure adhesive strength with the L-LDPE resin of the inner layer, have good film formability, reduce curling, are general-purpose resins and are inexpensive.
(1)低密度ポリエチレン樹脂( LDPE )(2)
中 1 (
!v!DPI)(3冫 高
1 (HDPE)(4)直鎖状低密度z
z ( L−LDPE )(5) エチレン・
グロビレン共重合体樹脂(ランダムあるいはブロック共
重合体樹脂等)(6) エチレン・ブテン1共重合体
樹脂(7) プロピレン
(8) エチレン・プロピレン・プテンl共重合体酎
脂(9) ポリプテン−1{封脂
αQ ポリスチレン樹脂
Oυ ポリメチル・メタクリレート樹脂(6)スチレン
・アクリロニトリル共重合体樹脂(至)ABS樹脂
α◆ ポリプロピレン樹脂
α時 結晶性プロピレンーα−オレフィン共重合体樹脂
(4)変性ポリプロピレン樹脂
αη I ポリエチレン l
α傍 ポリプロピレン・無水マレイン酸グラ7ト共重合
体樹脂
α@塩素化ホリオレフィン樹脂(主として塩素化?リエ
チレ/・樹脂) ( HDPE,LDPE,PEコポリ
マー,アタクチックpp等)
翰 エチレン・酢酸ビニル共重合体樹脂(EVA)a!
υ エチレン系アイオノマー樹脂(エチレンと不飽和酸
との共重合物を金属で架橋した樹脂)
(ハ) ポリ4−メチルベンテン−1樹脂翰 エチレン
・アクリル酸共重合体樹脂( FAA)(ハ) エチレ
ン・アクリル酸メチル共重合体樹脂( EMA )
(ハ) エチレン・アクリル酸エチル共重合体樹脂(
EEA )
(ニ)塩化ビニル・プロピレン共重合体樹脂(イ) エ
チレン番ビニルアルコール樹月旨(ハ)架橋ポリエチレ
ン樹脂(電子線照射架橋、化学的架橋等)
翰 ポリイノプチレン樹脂
(至)エチレンー塩化ビニル共重合体樹脂({1)
1.2−/リブタジニン樹脂等である。(1) Low density polyethylene resin (LDPE) (2)
Junior high school 1 (
! v! DPI) (3rd grade high school)
1 (HDPE) (4) Linear low density z
z (L-LDPE) (5) Ethylene・
Globylene copolymer resin (random or block copolymer resin, etc.) (6) Ethylene-butene-1 copolymer resin (7) Propylene (8) Ethylene-propylene-putene-1 copolymer fat (9) Polybutene-1 {Seal αQ Polystyrene resin Oυ Polymethyl methacrylate resin (6) Styrene-acrylonitrile copolymer resin (to) ABS resin α◆ Polypropylene resin α Crystalline propylene-α-olefin copolymer resin (4) Modified polypropylene resin αη I Polyethylene l α side Polypropylene/maleic anhydride graft copolymer resin α @ chlorinated polyolefin resin (mainly chlorinated polyolefin resin) (HDPE, LDPE, PE copolymer, atactic pp, etc.) Ethylene/vinyl acetate Copolymer resin (EVA) a!
υ Ethylene-based ionomer resin (resin in which a copolymer of ethylene and unsaturated acid is cross-linked with metal) (c) Poly 4-methylbentene-1 resin wire Ethylene-acrylic acid copolymer resin (FAA) (c) Ethylene・Methyl acrylate copolymer resin (EMA) (c) Ethylene/ethyl acrylate copolymer resin (
EEA ) (d) Vinyl chloride/propylene copolymer resin (a) Ethylene vinyl alcohol Jugetsuji (c) Crosslinked polyethylene resin (electron beam irradiation crosslinking, chemical crosslinking, etc.) Polyinoptylene resin (to) Ethylene-vinyl chloride copolymer resin Polymer resin ({1)
1.2-/ributazinine resin, etc.
本発明の中間層はヒートシール性、物理強度、耐摩耗性
、防湿性等に問題があっても内層と外層でカバーされる
。従って上記特性は変化させるか帯電防止性、遮光性の
良好な物質である帯電防止剤や導電性カーデンブラック
のアセチレンカーボンブラックや変性鼠生カーポンプラ
ックであるケッチェンカー〆ンブラックや金属粉末、炭
素峨維、金属繊維、グラファイト、表面を金属化した金
属メッキ7イラー、黒鉛繊fa導電性酸化亜鉛や錫、黒
鉛粉末、炭素質又は黒鉛質のウィスヵー状短繊維、ポリ
アルキレンオキシド系化合物、峨維状チタン酸カリウム
等を用いることができる。これらの帯電防止剤や導電性
粉末や4電性繊維は要求される導電性や用.途等Kより
単独あるいは混合して使用することが出来る。Even if the intermediate layer of the present invention has problems in heat sealability, physical strength, abrasion resistance, moisture resistance, etc., it is covered by the inner layer and the outer layer. Therefore, the above characteristics can be changed by using antistatic agents, which are substances with good antistatic and light-shielding properties, acetylene carbon black, which is conductive carden black, Ketjenker black, which is a modified rat carbon black, metal powder, and carbon thickener. Fibers, metal fibers, graphite, metal plating with a metalized surface, graphite fiber fa conductive zinc oxide or tin, graphite powder, carbonaceous or graphite whisker-like short fibers, polyalkylene oxide compounds, fibrillar Potassium titanate and the like can be used. These antistatic agents, conductive powders, and tetraelectric fibers meet the required conductivity and usage. They can be used alone or in combination.
これらの帯電防止剤や導電性物質の種類、形状、大きさ
、添加量は使用目的に応じて適宜選択しうる。ペースレ
ジンも最内層と最外層の樹脂組成に応じて適宜選択し5
るが、物理強度、経済性(安価)等の点から各種ポリオ
レフィン樹脂特に各種ぎりエチレン樹脂、α−オレフィ
ンとの共重合ポリプロピレン樹脂、EEA樹脂、EMA
樹脂、EAA樹脂、EvA樹脂、アイオノマー樹脂、接
着性?リマー等が好ましい。また中間層に市販の導電性
對脂例えば東京インキ(沫)製導電性グラスチック6パ
ピオスタット1、東洋インキ(株)製導電性プラスチッ
クスコンパウンド′゛リオコンダクト1、大日本インキ
化学(株)5導電性プラスチックス“グイエレック”等
を市販ベレットのtま又は他の樹脂とブレンドして用い
ることが好ましい。また、中間層は単一層の他複数層か
らなるよう形成しても.よい。本発明の外層は内層より
静摩擦係数(tanθ)内0,05以上大サく、且つ値
が0.19以上であることが必須であり、中間層との接
着強度が10,9/i5m巾以上であることが必須であ
る。The type, shape, size, and amount of these antistatic agents and conductive substances can be appropriately selected depending on the purpose of use. The pace resin is also selected appropriately depending on the resin composition of the innermost layer and outermost layer5.
However, from the viewpoint of physical strength, economical efficiency (inexpensive), etc., various polyolefin resins, especially ethylene resins, copolypropylene resins with α-olefins, EEA resins, EMA resins, etc.
Resin, EAA resin, EvA resin, ionomer resin, adhesiveness? Rimmer etc. are preferred. In addition, commercially available conductive resins may be used in the intermediate layer, such as conductive glasstic 6 Papiostat 1 manufactured by Tokyo Ink, conductive plastic compound '゛Rioconduct 1 manufactured by Toyo Ink Co., Ltd., and Dainippon Ink Chemical Co., Ltd. 5. It is preferable to use conductive plastics such as "Guierec" by blending them with commercially available pellets or other resins. Also, the intermediate layer may be formed from a single layer or from multiple layers. good. It is essential that the outer layer of the present invention has a coefficient of static friction (tan θ) larger than the inner layer by 0.05 or more and a value of 0.19 or more, and has an adhesive strength of 10.9/i5m or more with the intermediate layer. It is essential that
これらの点から前記中間層と略同種の熱可塑性樹脂を用
いるのが好ましく、前記中間層に用いる各種ポリオレ7
イン樹脂を主成分とすることが好ましい。From these points of view, it is preferable to use substantially the same type of thermoplastic resin as the intermediate layer.
Preferably, the main component is in-resin.
外層にも各種の熱可塑性樹脂や添加剤を混合することが
できるが、静摩擦係数が限定されるので添加量等は制限
される。これは静摩擦係数が内層と同等以下ですべりや
すいとフィルム成形工程、ラミネート工程、製袋工程、
製品包装後の物流工程で種々のトラブルが発生し実用化
が困難である。Although various thermoplastic resins and additives can be mixed in the outer layer, the amount added is limited because the coefficient of static friction is limited. This is because if the coefficient of static friction is equal to or lower than the inner layer and it is slippery, the film forming process, laminating process, bag making process, etc.
Various troubles occur during the logistics process after product packaging, making it difficult to put it into practical use.
本発明の同時多層共押し出しフィルムだけを用いて製造
する時は、外層は内層より5℃以上、好ましくは10℃
以上高い融点を有する熱可塑性樹脂を用いることが好ま
しい。例えば、HDPE樹脂、ポリエステル樹脂、ぼり
プロピレン樹脂、ポリアミド樹脂(各種ナイロン)アク
リル樹脂及び前記ポリオレ7イン樹脂との混合樹脂を用
いることが好ましい。外層Kは耐熱性、遮光性、防湿性
印刷適性、外観等が向上できるので光反射性遮光物質を
添加することも好ましい。When produced using only the simultaneous multilayer coextruded film of the present invention, the outer layer is 5°C or more higher than the inner layer, preferably 10°C.
It is preferable to use a thermoplastic resin having a higher melting point. For example, it is preferable to use HDPE resin, polyester resin, propylene resin, polyamide resin (various types of nylon), acrylic resin, and a mixed resin with the polyolefin resin. It is also preferable to add a light-reflecting light-shielding substance to the outer layer K since heat resistance, light-shielding properties, moisture-proofing properties, printability, appearance, etc. can be improved.
外層は静摩擦係数( tanθ)が内層よりO. O
S以上大きく且つ値が0.19以上である。静摩擦係数
が、このような条件を満たしていない場合Kは、フイル
ム間の滑りのためにフィルム成形工程、ラミネート工程
、製袋工程、裂品包装工程、及び物流工程で種々のトラ
ブルを発生し、実用にならない。The coefficient of static friction (tanθ) of the outer layer is O. O
S or more and the value is 0.19 or more. If the static friction coefficient does not meet these conditions, various troubles will occur in the film forming process, laminating process, bag making process, torn product packaging process, and logistics process due to slippage between the films. It's not practical.
中間層と内層及び外層間の接着強度はLoV15■巾以
上である。接着強度が10J7/15mm巾未満の場合
には、ラミネート工程、製袋工程、ヒートシール工程等
で層間剥離故障が発生する。層間剥離故障を生じた包装
体は遮光性、防湿性、ガスノ々リャ性など、写真感光材
料包装体として必要表機能を失う。The adhesive strength between the intermediate layer, inner layer and outer layer is LoV15 width or more. If the adhesive strength is less than 10J7/15mm width, delamination failure will occur during the lamination process, bag making process, heat sealing process, etc. A package in which delamination occurs loses functions necessary for a photographic material package, such as light-shielding properties, moisture-proofing properties, and gas-repellent properties.
内層、中間層及び外層には、カーゲンブラック以外の遮
光物質を添加してもよい。この遮光物質には光反射性遮
光性物質と光吸収性遮光性物質がある。A light-shielding substance other than Kagen black may be added to the inner layer, intermediate layer, and outer layer. This light-shielding substance includes a light-reflecting light-shielding substance and a light-absorbing light-shielding substance.
光反射性遮光物質としては、金属粉末、金属フレーク、
金属fI&維、白色顔料等が用いられる。金属粉末は金
属を粉末状に形成したものであり、アルミニウム粉末又
はアルミペーストより低揮発物質を除去した物が好まし
い。ここでアルミニウム粉末は溶融アルミニウムをアト
マイズ法、粒化法、回転円盤落下法、蒸発法等Kより粉
末状K形成されたものである。アルミニウム粉末単体で
は不安定であるのでアルミニウム粉末表面を不活性にす
る各種の公知の処理が施される。公知の合成樹脂充填用
金属粉末裂遣方法としては特開昭59−75931号公
報記載の方法等がある。Examples of light-reflecting light-shielding materials include metal powder, metal flakes,
Metal fI & fiber, white pigment, etc. are used. The metal powder is a metal formed into powder, and is preferably one in which less volatile substances are removed than aluminum powder or aluminum paste. Here, the aluminum powder is obtained by forming molten aluminum into powder form by an atomizing method, a granulation method, a rotary disk drop method, an evaporation method, or the like. Since aluminum powder alone is unstable, various known treatments are performed to make the surface of the aluminum powder inert. As a known method for splitting metal powder for filling synthetic resins, there is a method described in JP-A-59-75931.
また前記アルミペーストは、ボールミル法、スタンプミ
ル法又はアトマイズ法等の公知の方法でアルミニウム粉
末を作るときに、ミネラルスピリットと少僅のステアリ
ン酸又はオレイン酸等の高級脂肪酸の存在のもとにペー
スト状に作ったものである。In addition, the aluminum paste is made into a paste in the presence of mineral spirit and a small amount of higher fatty acids such as stearic acid or oleic acid when making aluminum powder by a known method such as a ball mill method, a stamp mill method, or an atomization method. It was made in the shape of
本発明の包装材料は、同時二層共押し出しフイルムだけ
で構成してもよいが、他のフレキシブルシ一ト層を積層
させて複合フィルムとして用いることもできる。The packaging material of the present invention may be composed of only a simultaneous two-layer coextruded film, but it can also be used as a composite film by laminating other flexible sheet layers.
複合フイルムに使用されろ他の7レキシプルシ一ト層と
しては、無延伸及び1軸分子配向、2軸分子配向した各
種の熱可塑性樹脂フイルム、例えば各種ポリエチレン樹
脂、ニチレン共重合体樹脂、ポリプロピレン樹脂、ポリ
塩化ビニル樹脂、ポリ塩化ビニリデン樹脂、ポリアミド
樹脂、ポリカーゲネート樹脂、ポリエステル樹脂などの
公知のフィルム、及びそれらの変性樹脂のフイルムがあ
る。The other seven lexical sheet layers used in the composite film include various non-stretched, uniaxially oriented and biaxially oriented thermoplastic resin films, such as various polyethylene resins, nethylene copolymer resins, polypropylene resins, There are known films of polyvinyl chloride resin, polyvinylidene chloride resin, polyamide resin, polycargenate resin, polyester resin, and films of modified resins thereof.
また、金属被膜加工フイルム(代表的なものはアルミニ
ウム真空蒸着フィルム)、アルミニウム真空蒸着紙、セ
ルローズアセテートフィルム、セロファン、?リビニル
アルコールフイルム、各種の紙、各植の金属ffi(代
表例としてアルミニウム箔)、不織布、ワリフ、穴開き
フィルム及びポリエチレン、ポリスチレン、ポリグロビ
レン、Iリウレタン等の発泡シート等の公知のフレキシ
ブルシ一ト層なども好適である。We also offer metal-coated film (typically aluminum vacuum-deposited film), aluminum vacuum-deposited paper, cellulose acetate film, cellophane, etc. Known flexible sheets such as ribinyl alcohol films, various papers, metal ffi of various types (aluminum foil as a typical example), nonwoven fabrics, warp sheets, perforated films, and foam sheets of polyethylene, polystyrene, polyglobylene, I-urethane, etc. Also suitable are layers.
複合フィルムとする場合には同時二層共押し出しフィル
ムの内層を製品と接する最内層に配置するのが防湿性、
ヒートシール性確保の為に必須である。When making a composite film, placing the inner layer of a simultaneous two-layer coextruded film as the innermost layer in contact with the product is the best way to achieve moisture resistance.
This is essential to ensure heat sealability.
複合フィルムとする方法は公知のあらゆる接着法により
可能であるが特に好ましいのはドライラミネート法とエ
クストルーシ,ンラミ不−ト法である。The composite film can be formed by any known adhesive method, but particularly preferred are the dry lamination method and the extrusion/in-lamination method.
エクストルーションラミネート法に用いられる特に好ま
しい接着剤はより具体的にいえば各種ポリエチレン樹脂
、ポリグロビレン樹脂、ポリプチレン樹脂、などポリオ
レ7イン樹脂からなる重合体及びニチレ,冫共重合体(
( EVA +ER4A + EEA等樹脂の他L−
LDPF.樹脂の如く、ニチレンに一部他のモノマー(
例えばα−オレフィン等))}を共重合させたもの、D
upont社のサーリン、三井ポリケミカル社のハイラ
ミン等のアイオノマー樹脂(イオン性共重合体)や三井
石油化学(株)のアドマー(接着性ポリマー)等がある
。Particularly preferable adhesives used in the extrusion lamination method are, more specifically, polymers made of polyolefin resins such as various polyethylene resins, polyglobylene resins, polybutylene resins, etc.
(EVA + ER4A + EEA and other resins L-
LDPF. Like resin, some other monomers (
For example, copolymerized α-olefin etc.)), D
Examples include ionomer resins (ionic copolymers) such as Surlyn from Upont and Hylamin from Mitsui Polychemicals, and Admer (adhesive polymer) from Mitsui Petrochemicals.
これらの接着剤は積層させようとするフレキシブルシ一
ト層より5°以上融点が低いものであることが好ましい
。この程度の温度差があればフレキシブルシ一トに悪影
響を与えず熱溶融接着を完全に行わせることができる。It is preferable that these adhesives have a melting point 5° or more lower than the flexible sheet layer to be laminated. If there is a temperature difference of this degree, it is possible to completely perform thermal melt bonding without adversely affecting the flexible sheet.
熱可塑性樹脂を用いたエクストルーションラミネート法
Kよる接着層の厚さは、通例6μm〜50μm好ましく
は10μm〜20μmとなるが、コスト、ラミネート速
度、積層体の全厚等に基いて定められるのでこの数値に
は特に限定されない。The thickness of the adhesive layer formed by extrusion lamination method K using thermoplastic resin is usually 6 μm to 50 μm, preferably 10 μm to 20 μm, but it is determined based on cost, lamination speed, total thickness of the laminate, etc. It is not particularly limited to numerical values.
写真感光材料とはハロrン化銀写真感光材料、ジアゾ写
真感光材料、ノアゾ系感光記録材料、感光性樹脂、自己
現像型写真感光材料、拡散転写型写真感光材料などであ
る。The photographic materials include silver halide photographic materials, diazo photographic materials, noazo photosensitive recording materials, photosensitive resins, self-developing photographic materials, and diffusion transfer photographic materials.
なお、本発明の包装材料は上記写真感光材料用はもちろ
ん光Kより変色したり、碩化劣化したりするすべての感
光物質及びチリや静電気により機能障害を起す物質代表
例としてIC用等の包装材料として最適である。The packaging material of the present invention can be used not only for the above-mentioned photographic light-sensitive materials, but also for all light-sensitive materials that discolor or degrade due to light K, as well as materials that cause functional problems due to dust and static electricity, such as IC packaging. It is ideal as a material.
本発明の包装材料を上記の写真感光材料に適用する場合
、1重平袋、2重平袋、角底浸、自立袋、1重ガゼ,ト
袋、2重ガゼット袋、フィルムシ一ト、防湿箱の内貼り
、リーダー紙等公知のあらゆる形態が可能である。When the packaging material of the present invention is applied to the above-mentioned photographic materials, single-layer flat bags, double-layer flat bags, square bottom bags, self-supporting bags, single-layer gusset bags, double-layer gusset bags, film sheets, All known forms such as lining inside a moisture-proof box, leader paper, etc. are possible.
製袋の方法は使用する積層フィルムの性質に応じてヒー
トシール、インノ々ルスシール、超音波シール、高周波
シールなど、従来公知のグラスチックフィルムのシール
法による。なお、また適宜の ゜接着剤、粘着剤などを
使用して裂袋することも可能である。The bag making method is based on conventionally known glass film sealing methods such as heat sealing, innolus sealing, ultrasonic sealing, and high frequency sealing, depending on the properties of the laminated film used. Furthermore, it is also possible to tear the bag using an appropriate adhesive or adhesive.
゛本発明の写真感光材料用包装材料では、内層が遮光性
、裂品挿入性、ブロッキング防止性、剥離帯電防止性、
防湿性、ガスバリャ性に優れている。゛In the packaging material for photographic light-sensitive materials of the present invention, the inner layer has light-shielding properties, breakage insertion properties, anti-blocking properties, peel-off antistatic properties,
Excellent moisture and gas barrier properties.
そして、ヒートシール性(ホットタック性、夾雑物シー
ル性、ヒートシール強度等)に優れているとともに経時
シール強度維持性に優れ、さらに物理強度も非常に優れ
ている。中間層は層間剥離を防止するだけでなく単一層
より内層と外層との接着強度をコントロールすることに
より物理強度を向上させることが出来る。高波長のカー
ゴンブラックを添加した場合は、物理強匣耐摩耗性、フ
イルム成形性、ヒートシール性、防湿性、印刷性、外観
に問題がある樹脂となるしかし、これらの特性は内層と
外層でカバーされるのでカーボンブラック等の帯電防止
遮光′吻質を10重量チ以上中間層に加えて静電防止性
ハクリ帯電防止性、遮光性等を改良できる。又中間層は
写真感光材料に接触しないので物理強度等の特性を向上
する個脂や添加剤で、写真感光材料に有害なものも加え
得る。In addition, it has excellent heat sealing properties (hot tack properties, contaminant sealing properties, heat sealing strength, etc.), excellent ability to maintain sealing strength over time, and further excellent physical strength. The intermediate layer not only prevents delamination but also improves physical strength by controlling the adhesive strength between the inner layer and the outer layer compared to a single layer. If high-wavelength cargoon black is added, the resin will have problems with physical strength, abrasion resistance, film formability, heat sealability, moisture resistance, printability, and appearance. Therefore, antistatic properties, antistatic properties, light blocking properties, etc. can be improved by adding 10% or more of antistatic light blocking material such as carbon black to the intermediate layer. Furthermore, since the intermediate layer does not come into contact with the photographic material, it is possible to add individual fats and additives that improve properties such as physical strength, but which are harmful to the photographic material.
最外層として最内層より0.05以上静摩擦係数を大き
くし、且つ値を0.19以上にすることによりフィルム
成形工程、ラミネート工程謙袋工程、製品包装後の物流
工程等の包装材料間のすべりのために発生する種々のト
ラブルを防止している。By increasing the static friction coefficient of the outermost layer by 0.05 or more than the innermost layer and setting the value to 0.19 or more, slippage between packaging materials during film forming process, laminating process, bagging process, logistics process after product packaging, etc. This prevents various troubles that may occur due to this.
外層に融点の高い熱可望性樹脂を用いたり、各種添加剤
を添加することにより、耐熱性を向上させて自動製袋適
性を向上させる。また反射性遮光物質を添加した場合は
防熱性や遮光性や外観や印刷通性、セーフライト下での
写真感光材料包装工程での表裏識別性等を良化すること
が出来る。By using a thermoplastic resin with a high melting point for the outer layer or adding various additives, heat resistance is improved and suitability for automatic bag making is improved. In addition, when a reflective light-shielding substance is added, it is possible to improve heat insulation, light-shielding properties, appearance, printability, front and back discrimination during the photographic material packaging process under safelight, etc.
本発叩による写真感光材料用包装材料の一実施例を第1
図に基づいて説明する。A first example of a packaging material for photographic light-sensitive materials produced by this punching process is shown in the first example.
This will be explained based on the diagram.
第1図は写真感光材料用包装材料の部分断面図である。FIG. 1 is a partial sectional view of a packaging material for photographic light-sensitive materials.
この例は本発明の最も基本となる層構成のもので、内層
1&、中間層2a及び外層3aの三層から成る同時多層
共押し出しフィルム4aのみから構成されている。This example has the most basic layer structure of the present invention, and is composed only of a simultaneous multilayer coextruded film 4a consisting of three layers: an inner layer 1&, an intermediate layer 2a, and an outer layer 3a.
第2図も写真感光材料用包装材料の他の例の部分断面図
である。この例は中間層2が多層に形成されており、中
央中間層21とその両側の内側中間層22及び外側中間
層23とから成っている。FIG. 2 is also a partial sectional view of another example of the packaging material for photographic materials. In this example, the intermediate layer 2 is formed in multiple layers, and includes a central intermediate layer 21 and an inner intermediate layer 22 and an outer intermediate layer 23 on both sides thereof.
そして内側中間層22に内層1が、外側中間層23に外
層3が積層されて5層からなる同時多層共押し出しフィ
ルム4&が形成されている。Then, the inner layer 1 is laminated on the inner intermediate layer 22, and the outer layer 3 is laminated on the outer intermediate layer 23, thereby forming a simultaneous multilayer coextruded film 4& consisting of five layers.
第3図も写真感光材料用包装材料の他の例の部分断面図
である。この例は第1図に示す同時多層共押し出しフィ
ルム4aに接着層5を介してフレキシブルシ一ト層6を
積層して形成したものである。FIG. 3 is also a partial sectional view of another example of the packaging material for photographic materials. In this example, a flexible sheet layer 6 is laminated on a simultaneous multilayer coextruded film 4a shown in FIG. 1 with an adhesive layer 5 interposed therebetween.
なお、第4図は比較品の部分断面図であり、本発明の内
層1aと滑剤が無添加以外は同一の{封脂組成で形成さ
れた遮光性L−LDPE *脂層7aのみからなるもの
である。In addition, FIG. 4 is a partial sectional view of a comparison product, which is the same as the inner layer 1a of the present invention except that no lubricant is added {light-shielding L-LDPE formed with a sealant composition *consisting only of a fat layer 7a It is.
次に、本発明品1及び2、比較品l1従来品1及び2の
各特性を比較した結果について説明する。Next, the results of comparing the characteristics of products 1 and 2 of the present invention, comparative product 11, and conventional products 1 and 2 will be described.
本発明品1は第1図の実施例に相当する。内層laは厚
さlOOμmであり、α−オレフィンが4ーメチルベン
テンーlのL−LDPE @脂である三井石油化学(株
)裏ウルトゼックス2021Lが96.33iiチ、フ
ァーネスカ一デンブラックが32&量襲、オレイン酸ア
ミド系滑剤であるライオン・アクゾ(沫)製アーモスリ
ップCDが0.07重量チの樹月旨で形成されている。The product 1 of the present invention corresponds to the embodiment shown in FIG. The inner layer la has a thickness of lOOμm, and the α-olefin is L-LDPE @ fat with 4-methylbentene-l, Mitsui Petrochemical Co., Ltd. Ura Urto Zex 2021L has a thickness of 96.33ii, Furnace Kaden Black has a thickness of 32mm. Armorip CD, manufactured by Lion Akzo, which is an oleic acid amide-based lubricant, is made of 0.07 weight chloride.
中間12aは、厚さ20μmであり、東洋インキ(株)
製導電性プラスチックスリオコンダクトPE COMP
245 8 0 iL量弥、三井石油化学(株)製ウ
ルトゼックス2021L 2 0重量一の樹脂で形成さ
れている。外層3aは、厚さ60μmであり、東洋アル
ミ(株)製アルミペーストを2重量係、三井石油化学(
株)製L−LDPE m脂ウルトゼックス60重量チ、
三井石油化学(株)製}IDPE i]14脂ハイゼッ
クス3300F 3 8重m%の樹脂で形成されている
。The middle layer 12a has a thickness of 20 μm and is manufactured by Toyo Ink Co., Ltd.
Conductive plastic slioconduct PE COMP
It is made of a resin having a weight of 245 80 iL and a weight of 2021L made by Mitsui Petrochemical Co., Ltd. The outer layer 3a has a thickness of 60 μm, and is made of 2 parts of aluminum paste manufactured by Toyo Aluminum Co., Ltd. and Mitsui Petrochemical (Mitsui Petrochemical Co., Ltd.).
Co., Ltd. L-LDPE m fat Urto Zex 60 weight chain,
It is made of Mitsui Petrochemical Co., Ltd. IDPE i] 14-fat HiZEX 3300F 3 8% by weight resin.
本発明品2は第1図の実施例に相当する。内層1aは厚
さが80μmである以外は本発明品1の内層1aと同じ
である。中間層2aは、厚さ20μmであり、大日本イ
ンキ化学(久製導電性プラステックスPE・29170
x量チ、日本ユニカー(株)製EEA樹脂NUC−61
70 (商標登録)30M量チの樹脂で形成されている
。外層3は、厚さ50μmであり、三井石油化学(株)
製HDPE樹脂ハイゼックス33DDF’30重量チL
,− LDPK樹脂ウルトゼックス2021L 7 0
n量チの樹脂で形成されている。比較品1は第4図の例
に相当し、厚さ150μmでL−LDPB樹脂であるα
−オレフィンが1−メチルペンテン−1の三井石油化学
(株)製ウルトゼックス2021L 8 0重量係と日
本ユニカ−(株) % NUCポリエチレン−1101
71 17重量%、三菱化学(株)製ファーネスカー
デンブラック4483M幻%の樹脂で形成されている。The product 2 of the present invention corresponds to the embodiment shown in FIG. The inner layer 1a is the same as the inner layer 1a of the product 1 of the present invention, except that the thickness is 80 μm. The intermediate layer 2a has a thickness of 20 μm and is manufactured by Dainippon Ink Chemical Co., Ltd. (Kyusei Conductive Plastics PE 29170).
x quantity, EEA resin NUC-61 manufactured by Nippon Unicar Co., Ltd.
70 (registered trademark) Made of 30M resin. The outer layer 3 has a thickness of 50 μm and is manufactured by Mitsui Petrochemical Co., Ltd.
Made of HDPE resin HIZEX 33DDF'30 weight Chi L
,-LDPK resin Urto ZEX 2021L 7 0
It is made of n amount of resin. Comparative product 1 corresponds to the example shown in FIG. 4, and has a thickness of 150 μm and is made of L-LDPB resin.
- Ultzex 2021L manufactured by Mitsui Petrochemicals Co., Ltd., whose olefin is 1-methylpentene-1 80 weight section and Nippon Unicar Co., Ltd. % NUC polyethylene-1101
71 17% by weight and Furnace Caden Black 4483M (manufactured by Mitsubishi Chemical Corporation) resin.
従来品Iは第5図の例だ相当し、厚さ150μmで、日
本ユニカー(株)製LDPE樹脂DFD−01197重
量チと三菱化成C株)!Aファーネスカーボンブラック
ス4B(商標登録)3重量チの樹脂で形成されてAる。Conventional product I corresponds to the example shown in Figure 5, has a thickness of 150 μm, and is made of LDPE resin DFD-01197 made by Nippon Unicar Co., Ltd. and Mitsubishi Kasei C Co., Ltd.). A Furnace Carbon Blacks 4B (registered trademark) is made of 3-weight resin.
従来品■は第6図の例に相当し、従来品■と同一樹脂組
成の厚さ52μmのLDPE樹脂遮光フィルム層8mに
厚さ15μmのLDPEエクストルージョン接着層5で
厚さ7μmのアルミニウム箔層9を積層する。そしてフ
レキシブルシ一ト層6としてヒネリ原紙355’/m2
を積層しさらに従来品■と同一樹脂組成の厚さ50μm
のLDPK樹脂遮光フイルム層8aを積層した7層構成
の積層フィルムよりなる包装材料である。Conventional product ■ corresponds to the example shown in Figure 6, and has the same resin composition as conventional product ■, with an 8 m thick LDPE resin light-shielding film layer of 52 μm thick, a 15 μm thick LDPE extrusion adhesive layer 5, and a 7 μm thick aluminum foil layer. Layer 9. And as flexible sheet layer 6, twisted base paper 355'/m2
50 μm thick with the same resin composition as the conventional product ■
This is a packaging material made of a seven-layer laminated film in which LDPK resin light-shielding film layers 8a are laminated.
以上本発明品1.n、比較品1、従来品1,Ifの特性
を比較した結果を第1表に示す。Above are the products of the present invention 1. Table 1 shows the results of comparing the characteristics of Comparative Product 1, Conventional Product 1, and If.
評価は下記による
優・・・非常に優れている 良・・・優れている可・
・・実用限反 改良必要・・・問題あり不可・
・・実用不可
A ヒートシール強度:
フィルム巾15亀のサンプルを2枚重ねて目的のシール
温度で、シール圧力1ゆ/(7n”、シール時間1秒条
件でヒートシールを行い、完全冷却後、シール面を18
0度角度で剥離するのに必要な荷重を求める。単位8/
15w巾、ヒートシール後1ケ月経時した時のヒートシ
ール強度を経時ヒートシール強度とした。The evaluation is as follows: Excellent: Very good Good: Fairly good
・Practical limit resistance Needs improvement ・Problems not possible ・
・・Not practical A Heat-sealing strength: Two samples with a film width of 15 mm are stacked and heat-sealed at the desired sealing temperature with a sealing pressure of 1Y/(7n” and a sealing time of 1 second), and after complete cooling, Seal surface 18
Find the load required to peel off at a 0 degree angle. Unit 8/
The heat sealing strength after 1 month of heat sealing with a width of 15W was defined as the heat sealing strength over time.
B ホットタック性(熱間シール性):160℃でヒー
トシールした直後の2枚の包装材料(巾15m)の開端
を片側45gの荷重で剥離角度22.5度で引張った場
合の熱間剥離距離(CM)により判定。B Hot tack property (hot sealability): Hot peeling when the open end of two packaging materials (width 15 m) immediately after heat sealing at 160°C is pulled at a peeling angle of 22.5 degrees with a load of 45 g on each side. Judging by distance (CM).
C 遮光性:
ASA I O Oの写真フィルムを各包装材料を使用
した袋に入れ完全密封後、8万ルックスの光に1時間さ
らし、遮光性を写真フィルムのカブリの程度により検出
、評価する。C. Light-shielding property: A photographic film of ASA IOO is placed in a bag made of each packaging material, completely sealed, and then exposed to light of 80,000 lux for 1 hour, and the light-shielding property is detected and evaluated by the degree of fog on the photographic film.
D 剥離帯電圧:
テストすべき包装材料を巾3. 5 cm ,長さ13
50簡のエンドレスベルトを作り、該エンドレスベルト
状包装材料を荷重5oo9の対向ローラ(上部SUS
tlll−ラ、下部SUS O−ラ)闇に12m/分の
スピードで送ったときの蓄電量をデルトメーターで測定
する。D Peeling voltage: The width of the packaging material to be tested is 3. 5 cm, length 13
A 50-piece endless belt was made, and the endless belt-like packaging material was passed through opposing rollers (upper part made of SUS) with a load of 5oo9.
tllll-ra, lower SUS O-ra) Measure the amount of stored electricity with a deltmeter when sending it into darkness at a speed of 12 m/min.
E 静摩擦係数:
テストすべきシートの1部を切取り、これを縦7 5
m X 3 5■の荷重200gのブロックの底面に貼
着する。一方、テストすべきシートの1部を同様に切取
って傾斜面に貼着し、前記ブロックのシート面を傾斜面
上に載せ、この傾斜面の傾斜角度を変化させて、前記ブ
ロックが滑り始めた角度θを読み取った後tinθとし
て求めた値
例 滑り始めた角度 30度なら靜傘療簗改まtan3
0度= となる15度 # # Fin15度
”I IF 製袋適性:
写真感光材科を包装材料で自動表袋により3方シール袋
に包装した時のビンホール発生しにくさ、ヒートシール
適性、製品挿入性、等より判定。E Static friction coefficient: Cut out a part of the sheet to be tested and cut it lengthwise 7 5
Attach it to the bottom of a block measuring 200 g (m x 3 5 cm) and weighing 200 g. On the other hand, a part of the sheet to be tested is similarly cut out and pasted on an inclined surface, the sheet surface of the block is placed on the inclined surface, and the inclination angle of this inclined surface is changed, and the block begins to slide. An example of the value obtained as tinθ after reading the angle θ.
0 degrees = 15 degrees # # Fin15 degrees"I IF Bag making suitability: Difficulty in generating bottle holes when photosensitive materials are packaged into 3-side seal bags using automatic top bags, suitability for heat sealing, and product Judging from insertability, etc.
G 包装材料取扱い性:
フィルム成形工程、ラミネート工程、製袋工程、物流工
程等のトータル取扱い性より判定〔発明の効果〕
本発明は以上のように構成したので、内層及び外層で物
理強度、防湿性、がスバリャー性、ヒートシール性等を
充分に確保できる。また、中間層は、物理強度等は内層
及び外層が確保するので充分でなくてもよく、帯電防止
物質を多量に添加することができ、帯電防止性を向上さ
せることができる。又、中間層にはこれらの特性を具備
し、安価であるものの、写真感光材料に有害な物質も添
加できる。従って、包装材料全体として、物理強度、帯
電防止性等が良好で、かつ大幅に薄肉化が可能で安価に
提供できる。G. Packaging material handling properties: Judgment based on total handling properties such as film forming process, laminating process, bag making process, logistics process, etc. [Effects of the invention] Since the present invention is configured as described above, physical strength and moisture resistance are achieved in the inner and outer layers. It is possible to ensure sufficient properties such as properties, properties, heat sealability, etc. Further, the intermediate layer does not need to be sufficient because physical strength and the like are ensured by the inner layer and the outer layer, and a large amount of antistatic substance can be added to improve antistatic properties. Further, although the intermediate layer has these characteristics and is inexpensive, it can also contain substances harmful to the photographic material. Therefore, the packaging material as a whole has good physical strength, antistatic properties, etc., can be made significantly thinner, and can be provided at low cost.
第1図から第3図はいずれも本発明の実施例である包装
材料の部分断面図である。第4図は比較品の部分断面図
である。第5図及び第6図は従来の包装材料の部分断面
図である。
1・・・内層、2・・・中間層、3・・・外層、4・・
・同時多層共押し出しフィルム
aは遮光物質を含むことを意味する。
特許出願人 富士写真フイルム株式会社代理人弁理士
田 中 政 浩 ほか1名第1図
第3図
第5図
[7P・
第2図
第4図
第6図1 to 3 are partial cross-sectional views of packaging materials that are embodiments of the present invention. FIG. 4 is a partial sectional view of a comparative product. 5 and 6 are partial cross-sectional views of conventional packaging materials. 1...Inner layer, 2...Middle layer, 3...Outer layer, 4...
- Simultaneous multilayer coextrusion film a means that it contains a light-shielding substance. Patent applicant Fuji Photo Film Co., Ltd. Representative Patent Attorney
Masahiro Tanaka and 1 other person Figure 1 Figure 3 Figure 5 [7P/ Figure 2 Figure 4 Figure 6
Claims (3)
鎖状低密度ポリエチレン樹脂が30〜99.49重量%
、カーボンブラックが0.5〜10重量%そして滑剤が
0.01〜1.00重量%のヒートシール層であって静
摩擦係数が0.12〜0.37である内層と、熱可塑性
樹脂で形成された中間層と、熱可塑性樹脂で形成され静
摩擦係数が内層より0.05以上大きくかつその絶対値
が0.19以上である外層とから成り、該内層と中間層
及び外層と中間層の接着強度が10g/15mm巾以上
である同時多層共押し出し遮光フィルムを具備している
ことを特徴とする写真感光材料用包装材料(1) Linear low density polyethylene resin, which is a copolymer of ethylene and α-olefin, is 30 to 99.49% by weight
, a heat-sealing layer containing 0.5 to 10% by weight of carbon black and 0.01 to 1.00% by weight of a lubricant, and an inner layer having a static friction coefficient of 0.12 to 0.37, and a thermoplastic resin. an outer layer made of a thermoplastic resin and having a coefficient of static friction 0.05 or more larger than the inner layer and an absolute value of 0.19 or more, and the adhesive between the inner layer and the intermediate layer and the outer layer and the intermediate layer. A packaging material for photographic materials characterized by comprising a simultaneous multilayer coextruded light-shielding film having a strength of 10 g/15 mm or more.
数6ケ以上のα−オレフィンとの共重合体樹脂からなる
特許請求の範囲第1項の記載の写真感光材料用包装材料(2) The packaging material for photographic materials as set forth in claim 1, wherein the linear low-density polyethylene resin is a copolymer resin of ethylene and an α-olefin having 6 or more carbon atoms.
はエチレン共重合体樹脂のいずれか1つ以上を30重量
%以上含む特許請求の範囲第1項又は第2項記載の写真
感光材料用包装材料(3) The packaging material for photographic materials according to claim 1 or 2, wherein the thermoplastic resin in the outermost layer contains 30% by weight or more of any one or more of various polyethylene resins or ethylene copolymer resins.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61144758A JPH0629954B2 (en) | 1986-06-23 | 1986-06-23 | Packaging material for photographic light-sensitive material and packaging method for photographic light-sensitive material |
US07/064,654 US4876129A (en) | 1986-06-23 | 1987-06-22 | Packaging material for photographic photosensitive materials |
DE19873720743 DE3720743C2 (en) | 1986-06-23 | 1987-06-23 | Packaging material for light-sensitive photographic materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61144758A JPH0629954B2 (en) | 1986-06-23 | 1986-06-23 | Packaging material for photographic light-sensitive material and packaging method for photographic light-sensitive material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS631540A true JPS631540A (en) | 1988-01-06 |
JPH0629954B2 JPH0629954B2 (en) | 1994-04-20 |
Family
ID=15369711
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61144758A Expired - Fee Related JPH0629954B2 (en) | 1986-06-23 | 1986-06-23 | Packaging material for photographic light-sensitive material and packaging method for photographic light-sensitive material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0629954B2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01316742A (en) * | 1988-06-17 | 1989-12-21 | Fuji Photo Film Co Ltd | Packaging material for photosensitive material |
JPH0244738U (en) * | 1988-09-22 | 1990-03-28 | ||
JPH02278255A (en) * | 1989-04-20 | 1990-11-14 | Fuji Photo Film Co Ltd | Packaging material for photosensitive material |
JPH02278256A (en) * | 1989-04-20 | 1990-11-14 | Fuji Photo Film Co Ltd | Packaging material for photosensitive material |
JPH04124656A (en) * | 1990-09-15 | 1992-04-24 | Takeda Sangyo:Kk | Light shieldable packaging material |
JP2015189133A (en) * | 2014-03-28 | 2015-11-02 | 積水化成品工業株式会社 | Resin expanded sheet for deep draw molding, container, and method of manufacturing these |
-
1986
- 1986-06-23 JP JP61144758A patent/JPH0629954B2/en not_active Expired - Fee Related
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01316742A (en) * | 1988-06-17 | 1989-12-21 | Fuji Photo Film Co Ltd | Packaging material for photosensitive material |
JPH0244738U (en) * | 1988-09-22 | 1990-03-28 | ||
JPH02278255A (en) * | 1989-04-20 | 1990-11-14 | Fuji Photo Film Co Ltd | Packaging material for photosensitive material |
JPH02278256A (en) * | 1989-04-20 | 1990-11-14 | Fuji Photo Film Co Ltd | Packaging material for photosensitive material |
JPH04124656A (en) * | 1990-09-15 | 1992-04-24 | Takeda Sangyo:Kk | Light shieldable packaging material |
JP2015189133A (en) * | 2014-03-28 | 2015-11-02 | 積水化成品工業株式会社 | Resin expanded sheet for deep draw molding, container, and method of manufacturing these |
Also Published As
Publication number | Publication date |
---|---|
JPH0629954B2 (en) | 1994-04-20 |
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