JPH0562571B2 - - Google Patents
Info
- Publication number
- JPH0562571B2 JPH0562571B2 JP61146561A JP14656186A JPH0562571B2 JP H0562571 B2 JPH0562571 B2 JP H0562571B2 JP 61146561 A JP61146561 A JP 61146561A JP 14656186 A JP14656186 A JP 14656186A JP H0562571 B2 JPH0562571 B2 JP H0562571B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- vinyl chloride
- chloride resin
- roll
- fine powder
- 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.)
- Expired - Lifetime
Links
- 239000000843 powder Substances 0.000 claims description 41
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 35
- 229920005989 resin Polymers 0.000 claims description 34
- 239000011347 resin Substances 0.000 claims description 34
- 239000004014 plasticizer Substances 0.000 claims description 15
- 229920002472 Starch Polymers 0.000 claims description 14
- 239000008107 starch Substances 0.000 claims description 14
- 235000019698 starch Nutrition 0.000 claims description 14
- 238000004804 winding Methods 0.000 claims description 12
- 238000001125 extrusion Methods 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 239000010445 mica Substances 0.000 claims description 9
- 229910052618 mica group Inorganic materials 0.000 claims description 9
- 238000000465 moulding Methods 0.000 claims description 9
- 238000005507 spraying Methods 0.000 claims description 7
- 239000011342 resin composition Substances 0.000 claims description 6
- 229920002545 silicone oil Polymers 0.000 claims description 5
- 150000002222 fluorine compounds Chemical class 0.000 claims description 2
- 238000000034 method Methods 0.000 description 25
- 230000000181 anti-adherent effect Effects 0.000 description 18
- 230000037303 wrinkles Effects 0.000 description 14
- 239000000454 talc Substances 0.000 description 10
- 229910052623 talc Inorganic materials 0.000 description 10
- 239000000463 material Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 6
- -1 Vinylidene halide compounds Chemical class 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 239000002981 blocking agent Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 238000005755 formation reaction Methods 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- DNUPYEDSAQDUSO-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl benzoate Chemical compound OCCOCCOC(=O)C1=CC=CC=C1 DNUPYEDSAQDUSO-UHFFFAOYSA-N 0.000 description 2
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- ZFOZVQLOBQUTQQ-UHFFFAOYSA-N Tributyl citrate Chemical compound CCCCOC(=O)CC(O)(C(=O)OCCCC)CC(=O)OCCCC ZFOZVQLOBQUTQQ-UHFFFAOYSA-N 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- UDHHXYYEUWKHMF-UHFFFAOYSA-N 6-butoxy-6-oxohexanoic acid Chemical compound CCCCOC(=O)CCCCC(O)=O UDHHXYYEUWKHMF-UHFFFAOYSA-N 0.000 description 1
- QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
- PYGXAGIECVVIOZ-UHFFFAOYSA-N Dibutyl decanedioate Chemical compound CCCCOC(=O)CCCCCCCCC(=O)OCCCC PYGXAGIECVVIOZ-UHFFFAOYSA-N 0.000 description 1
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241000237858 Gastropoda Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 241000519995 Stachys sylvatica Species 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- SHLNMHIRQGRGOL-UHFFFAOYSA-N barium zinc Chemical compound [Zn].[Ba] SHLNMHIRQGRGOL-UHFFFAOYSA-N 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000006084 composite stabilizer Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- UCVPKAZCQPRWAY-UHFFFAOYSA-N dibenzyl benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC=2C=CC=CC=2)C=1C(=O)OCC1=CC=CC=C1 UCVPKAZCQPRWAY-UHFFFAOYSA-N 0.000 description 1
- PUFGCEQWYLJYNJ-UHFFFAOYSA-N didodecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCC PUFGCEQWYLJYNJ-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- BPJZKLBPJBMLQG-KWRJMZDGSA-N propanoyl (z,12r)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OC(=O)CC BPJZKLBPJBMLQG-KWRJMZDGSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- 238000009966 trimming Methods 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
- Winding Of Webs (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Description
「産業上の利用分野」
本発明は、粘着性及び表面外観を改良した軟質
塩化ビニル系フイルムの製造方法に関する。更に
詳しくは従来の粘着性を改良するために粘着防止
微粉末をフイルム表面に散布するために生じる粘
着防止微粉末のフイルム表面へのめり込み、透明
性の低下、アバタ状の発生、ロール巻状物のシワ
及びフシの発生等を改良した粘着性及び表面外観
の良好な軟質塩化ビニル系樹脂フイルムの製造方
法に関するものである。
「従来の技術」
塩化ビニル系樹脂に多量の可塑剤を配合した軟
質塩化ビニル系樹脂フイルムは、一般にはカレン
ダー成形法又は押出成形法によつて連続的に製造
され、フイルムはロール状に巻き取られる。
軟質塩化ビニル系樹脂フイルムは日用雑貨品、
衣類等の包装用、農業用ハウス被覆用等用途は多
岐にわたる。そして、一般に各々の用途に応じ
て、ロール巻状物から巻き戻し、裁断、ウエルダ
ー加工、印刷等のいわゆる二次加工がほどこされ
る。
塩化ビニル系樹脂100重量部に対し、可塑剤を
25重量部以上配合してフイルム化した軟質塩化ビ
ニル系樹脂フイルムは、表面の平滑度が高く、透
明性が良好であるが、フイルム表面が粘着性を示
し、ロール状に巻いた時にフイルム表面同士が付
着しあう。このように表面同士が相互に付着しあ
つたロール状フイルムは、二次加工する際に巻き
戻しにくく、作業性が極めて悪くなるばかりでな
く、場合によつては二次加工により得られた製品
の表面同士が付着しあい、不良品となることもあ
る。
このような問題を排除する方法として、軟質塩
化ビニル系樹脂フイルムをカレンダー成形法又は
押出成形法により連続的に製造し、これをロール
状に巻き取る直前に、フイルム表面にデンプン、
タルク等の粘着防止微粉末を散布する方法が提案
され、実用化されている。
「発明が解決すべき問題点」
一般的に軟質塩化ビニル系樹脂フイルムをカレ
ンダー成形法、又は押出成形法により連続的に製
造し、これをロール状に巻き取る直前に粘着防止
微粉末を散布する方法においては、フイルム温度
が十分に冷却されていないため、散布したデンプ
ン、タルク等の粘着防止微粉末がフイルム表面に
めり込み、フイルム表面が梨地状となり、平滑度
を失ない、透明性が悪くなる傾向があつた。
上記の問題を解決するために、巻き取る時のフ
イルムの温度を低くしてみた結果、巻き取りフイ
ルムにシワが発生したり、巻き取つたフイルムの
ロール巻状物がリンクルと称する波うち(凸凹)
を生じる傾向があつた。
又、カレンダー成形法、押出成形法により連続
的に製造し、これをロール状に巻き取る直前に粘
着防止微粉末を散布した場合、フイルム表面がす
べりやすくなるため、エアーを巻き込み、このエ
アーを巻き込んだ部分がアバタ状になり、外観を
悪くしたり、又巻き硬さがゆるくなり、巻き上が
つたロール巻状フイルムを移送する時や保管時に
打痕が発生する等の傾向があつた。
「問題点を解決するための手段」
本発明者らはかかる状況にあつて、軟質塩化ビ
ニル系樹脂フイルムの表面の平滑性、透明性を失
わず粘着防止剤のフイルム表面へのめり込みやエ
アーの巻き込みによるアバタ状の発生がなく、ロ
ール巻状物にフシ、シワ入り、リンクルの発生が
なく、ロール巻状物の巻きが硬く、打痕のつかな
い、粘着性及び表面外観の良好な軟質塩化ビニル
系樹脂フイルムの製造方法を提供することを目的
として、鋭意検討した結果、本発明を完成するに
至つたものである。
しかして、本発明の要旨とするところは、塩化
ビニル系樹脂100重量部及び可塑剤25〜100重量部
を含む樹脂組成物をカレンダー成形法又は押出成
形法によりフイルム化し、ロール巻状に巻き取
り、冷却し、後にこのロール巻状物を巻き戻し、
少なくともフイルムの片面に粘着防止微粉末を散
布して巻き取ることを特徴とする粘着性及び表面
外観良好な軟質塩化ビニル系樹脂フイルムの製造
方法に存する。
以下、本発明を詳細に説明する。
本発明において塩化ビニル系樹脂とは、ポリ塩
化ビニルおよび塩化ビニルを主体とする共重合体
を意味する。塩化ビニルと共重合しうるモノマー
としては、ビニルエステル類、ビニルエーテル
類、アクリル酸またはメタクリル酸およびこれら
のエステル類、マレイン酸またはフマール酸およ
びこれらのエステル類、ならびに無水マレイン
酸、芳香酸ビニル化合物、ハロゲン化ビニリデン
化合物、アクリロニトリル、メタクロニトリル、
エチレン、プロピレンなどがあげられる。
上記塩化ビニル系樹脂を軟質化するには、樹脂
100重量部に対して、可塑剤25〜100重量部を配合
する。
使用しうる可塑剤としては、ジオクチルフタレ
ート、ジブチルフタレート、ブチルベンジルフタ
レート、ジベンジルフタレート、ジイソデシルフ
タレート、ジドデシルフタレート、ジウデシルフ
タレート等のフタル酸エステル類;アジピン酸ジ
オクチル、アジピン酸−n−ブチル、セバシン酸
ジブチル等の脂肪族二塩基酸エステル類;ペンタ
エリスリトールエステル、ジエチレングリコール
ベンゾエート等のグリコールエステル類;アセチ
ルリシノール酸メチル等の脂肪酸エステル;トリ
クレジルホスフエート、トリキシレニルホスフエ
ート等のりん酸エステル類;エポキシ化大豆油、
エポキシ化アマニ油、ジグリシジルビスフエノー
ルA等のエポキシ化合物;アセチルトリブチルシ
トレート、アセチルトリオクチルシトレート、ト
リ−n−ブチルシトレート等のクエン酸エステル
類、トリアルキルトリメリテート、テトラ−n−
オクチルピロメリテート、ポリプロピレンアジペ
ート、その他ポリエステル系等の種々の構造の可
塑剤があげられる。
塩化ビニル系樹脂には、上記可塑剤のほか、必
要に応じて通常の各種樹脂添加物、例えば安定
剤、滑剤、防曇剤、帯電防止剤、酸化防止剤、紫
外線吸収剤、光安定剤、染料、顔料、充填材、難
燃剤等を配合することができる。
これら樹脂添加物は、通常の配合量、例えば基
体の塩化ビニル系樹脂100重量部当り、10重量部
以下の範囲で選ぶことができる。
塩化ビニル系樹脂の可塑剤、各種樹脂添加物を
配合するには、通常の混合、配合技術、例えばリ
ボンブレンダー、バンバリーミキサー、スーパー
ミキサーその他従来から知られている配合機、混
合機を使用すればよい。
本発明方法では、前記可塑剤の配合された塩化
ビニル系樹脂組成物を、フイルム状とする。前記
塩化ビニル系樹脂組成物をフイルム化するには、
Tダイ法、インフレーシヨン法等の押出成形法、
及びカレンダー成形法の技術が採用される。
フイルムは所望幅に、0.03mm〜1mmの範囲の所
望の厚さにフイルム状に製膜後一旦ロール状に巻
き取る。巻き取り方法は従来公知のものでよく、
例えばセンターワインダー、サーフエスワインダ
ー等によつて巻き取り、ロール状の製品とする。
この時の巻き取り温度はシワが入らない温度で
良いが、好ましくは20℃〜60℃が良い。巻き取り
温度を20℃より低くすると巻き取り時のシワの発
生が生じ易くなり好ましくない。又、巻き取り温
度を60℃より高くするとフイルム巻き戻しが重く
なるので好ましくない。
本発明方法では上記ロール状に巻き取つたフイ
ルムの各部分が均一に冷却固化したのち巻き戻
し、このフイルムの少なくとも片面に粘着防止微
粉末を散布し、再度ロール状に巻き取る。
本発明方法で用いられる粘着防止微粉末は、ジ
ヤガイモ、トウモロコシ、コムギなどの植物から
得られるデンプン微粉末、タルク、四ケイ素雲母
等、従来粘着防止微粉末として使用されているい
ずれのものでも良い。
上記デンプン微粉末、タルク、四ケイ素雲母は
吸湿性があるので、これを表面に散布したフイル
ムを長期間保存しておくと、粒子が吸湿して凝集
する性質があるので、フイルム同士の粘着防止の
機能が低下することがある。この経時変化による
粘着防止機能の低下を防止または抑制する目的
で、デンプン微粉末の表面を、あらかじめ他の物
質で被覆されたものを用いるのが好ましい。
デンプン微粉末、タルク、四ケイ素雲母の粒子
表面を被覆するのに好ましい物質としては、シリ
コンオイル、フツ素化合物等があげられる。
シリコンオイルの具体例としては、シロキサン
結合を骨格とし、ケイ素原子にメチル基、フエニ
ル基、水酸基等をもつたシリコンオイルであり、
ジメチルポリシロキサン、ジフエニルポリシロキ
サン、メチルフエニルポリシロキサン、ジメチル
ーメチルフエニルポリシロキサン、ジメチルージ
フエニルポリシロキサン、メチルハイドロジエン
ポリシロキサン等があげられる。フツ素系化合物
としては、四フツ化エチレン樹脂のオリゴマー、
末端にアクリレート、メタクリレートなどの官能
基を有するパーフルオロアルキル基を含むフツ素
系化合物があげられる。
デンプン微粉末、タルク、四ケイ素雲母等の粒
子の表面を上記物質で被覆するには、上記シリコ
ンオイル、フツ素系化合物等を溶媒に分散または
溶解し、これにデンプン微粉末を加えて混合し、
溶媒を揮散させればよい。
本発明に従い、フイルム表面の少なくとも片面
に上記デンプン微粉末、タルク、四ケイ素雲母等
の粘着防止微粉末の散布は、カレンダー系列、あ
るいは押出系列で製膜された塩化ビニル系樹脂フ
イルムを一旦長尺広巾のロール巻に巻き取り、フ
イルムの各部分の温度が均一になるよう冷却固化
したのち、このロール巻状のフイルムを巻き戻
し、静電気除去装置によりフイルム表面の静電気
を除去した後とする。
ロール巻状のフイルムを巻き戻す時のフイルム
温度は、デンプン微粉末、タルク、四ケイ素雲母
等の粘着防止微粉末がフイルム表面にめり込み、
粘着防止微粉末がフイルムに凹みを生じさせた
り、フイルムに付着しない温度ならよく、フイル
ムに含まれる可塑剤量により異なるが、好ましく
は10℃〜30℃が良い。フイルム温度が10℃より低
くなるとフイルムの柔軟性がなくなり、両端をト
リムした場合に破れる等のトラブルが生じ易くな
るので好ましくない。
又フイルム温度が30℃より高くなるとフイルム
表面が柔らかくなり、粘着防止剤がフイルムにめ
り込んだり、フイルムに付着し、フイルム外観が
梨地状になり、透明性も悪くなるので好ましくな
い。
又本発明において用いるデンプン微粉末、タル
ク、四ケイ素雲母等の粒子径は1〜30ミクロンの
範囲が好ましい。平均粒子径が1ミクロンより小
さいと、粒子同士が凝集し、ボタ落ちと称する大
きなかたまりとなつてフイルム表面に落下し、フ
イルム表面の平滑性を失うことがあり、好ましく
ない。又平均粒子径が30ミクロンより大きいと、
フイルムをロール巻状にする時フイルムの間にエ
アーの巻き込みが多くなり硬巻にできず、ロール
巻の移送、保管時に打痕を生じる等の問題が発生
し、好ましくない。
フイルム表面へのデンプン微粉末、タルク、四
ケイ素雲母等の粘着防止剤の散布法は、静電気に
よる粒子の帯電を利用した静電ダスター、回転ド
ラムによるスプレー機等の従来から知られている
装置を用いる方法によればよい。
フイルム表面への散布量は、フイルムに配合す
る可塑剤の種類、可塑剤の配合量、フイルムの二
次加工方式等によつて種々選ぶことができ、フイ
ルム1m2あたり0.01〜5グラムの範囲とするのが
好ましい。散布量が0.01g/m2より少ないと、フ
イルム表面の粘着防止効果が少なくなり、5g/
m2より多いとフイルム間がすべり過ぎて十分な硬
巻のロール巻ができなかつたり、二次加工時トラ
ブルが生じることがあり好ましくない。
「発明の効果」
以上のような方法でカレンダー成形法、押出成
形法により製膜された軟質塩化ビニル系樹脂フイ
ルムを長尺広巾のロール巻状に巻き取り、均一に
冷却固化したのち巻き戻し、このフイルムの少な
くとも片面に粘着防止微粉末を散布し、再度ロー
ル巻に巻き取つたフイルムは、従来のカレンダー
成形法、押出成形法により製膜された塩化ビニル
系樹脂フイルムをロール状に巻き取る前に、フイ
ルム粘着防止微粉末を散布したフイルムと比較す
ると、下記に示すような特別に顕著な効果を奏
し、その産業上の利用価値は極めて大である。
(1) 本発明によつて得られた軟質塩化ビニル系樹
脂フイルムは粘着防止微粉末が軟質塩化ビニル
系樹脂フイルムにめり込まず、又フイルム表面
に粘着しないため、フイルムの平滑性が良く、
透明性も極めて良好である。
(2) 本発明方法によれば粘着防止微粉末がフイル
ムにめり込まず、又フイルム表面に粘着しない
ため従来方法と比較し、少量の粘着防止微粉末
の散布により粘着防止効果が生じるため経済
的、衛生的であり、また二次加工後の製品にお
いて粘着防止微粉末による悪影響を防止でき
る。
(3) 本発明によれば粘着防止微粉末がフイルムに
めり込まず、又フイルム表面に粘着しないた
め、特別に粘着防止効果が必要で多量の粘着防
止微粉末を散布した場合にもフイルムの表面外
観への悪影響はない。
(4) 本発明によればロール巻状のフイルム間のエ
アーの巻き込みによるアバタ状の外観不良が生
じず、表面平滑性、透明性が良好なフイルムが
得られる。
(5) 本発明によれば粘着防止微粉末を散布するフ
イルムは均一に冷却固化されているため、従来
法に比較し、大きな張力で巻き取つてもフイル
ムに歪みが生じにくく、巻きの硬いロール巻が
得られるため、ロール巻の移送時、保管時にお
こる打痕(凹み)が生じにくく、フイルムの表
面外観が損なわれない。
(6) 本発明によればフイルム各部が均一に冷却固
化されているため、従来法に比較してシワ(巻
き込みジワ)の発生がない表面外観の良好なフ
イルムが得られる。
(7) 本発明によれば粘着防止微粉末を均一に冷却
固化されたフイルム表面に散布した後、ロール
状に巻き取るため、ロール巻き後のフイルム収
縮がほとんど発生せず、フイルム厚薄部分によ
るロール巻状物のフシ(凸凹)の発生がなく、
ロール巻状物の均一な円筒形が、維持され、ロ
ール巻状物からフイルムを巻き戻した場合の平
滑性(レイフラツト性)が良好である。
以下、本発明を実施例、比較例にもとづいて詳
細に説明するが、本発明はその要旨を越えない限
り、以下の例に限定されるものではない。
実施例 1
ポリ塩化ビニル(=1100) 100重量部
ジオクチルフタレート 第1表に示した通り
バリウム−亜鉛系複合安定剤 2重量部
エポキシ化大豆油 3 〃
よりなる原料、樹脂添加物を秤量した。これらを
スーパーミキサーで10分間攪拌混合した後、170
℃に加熱したロール上で混練し、逆L型カレンダ
ー装置により、幅1000mm、厚さ0.1m/mの透明
な軟質塩化ビニルフイルムに圧延し、フイルム化
した。このフイルムをクーリング装置により45℃
まで冷却したのちワインダー装置により1000mの
長さに、ロール状に巻き取つた。
上記ロール巻きを24時間放置し、フイルム温度
が20℃にてこのロール巻きからフイルムを巻き戻
し、このフイルムの片面に、ドラム方式の微粉末
スプレー機(ニツカ・スプレー装置)で、デンプ
ン微粉末(ニツカ株式会社製AS−100、平均粒子
径15ミクロン)をフイルム1平方m当り0.1g散
布し、フイルム両端を切断後、巾970mm、巻き長
さ100m巻きのロール状に巻き取つた。
実施例 2〜17
実施例1の粘着防止剤の種類、散布量、原反可
塑剤の配合量、原反巻取温度、粘着防止剤散布等
のフイルム温度を第1表のように変化させ、それ
以外は実施例1と同一の方法で16種のロール巻き
を製造した。
比較例 1〜6
実施例1と同一のポリ塩化ビニル系樹脂組成物
を実施例1と同一の方法で混合、混練し、逆L型
カレンダー装置により幅1000m/m、厚さ0.1
m/mの透明な軟質塩化ビニルフイルムに圧延し
た。
カレンダーロールから出たあとのフイルムを、
クーリングロールに接触させてフイルム温度を第
1表に示した種々の温度まで冷却し、第1表に示
した種々の微粉末を第1表に示した散布量に調節
して散布した。このフイルムをワインダーにて
100m長さのロール巻状に巻き取つた。実施例及
び比較例で製造した23種の軟質塩化ビニル系樹脂
フイルムのロール巻きを温度25℃、相対湿度90%
とした雰囲気下で、2週間放置したあと、次の方
法によつてフイルムの粘着性、表面平滑性、透明
性、アバタ発生、シワ発生、フシの発生、レイフ
ラツト性、巻き硬さについて観察評価を実施し
た。第1表に示した評価結果は次の意味を有す
る。
「フイルムの粘着性」
○……粘着性ほとんどなし
△……粘着性若干あり
×……粘着性著しくあり
「表面平滑性」
上の粘着性の評価を行なつたフイルムの表面
を、肉眼で観察した。第1表に示した評価結果
は、次の意味を有する。
○……表面は極めて平滑である
△……表面に粉のめり込みによる若干の凹凸が認
められる
×……表面に粉のめり込み、付着によるかなりの
凹凸が認められる
「透明性」
ロール状物から切り出したフイルムを、光源に
向けてかざし、透明性を肉眼で判定した。第1表
に示した評価結果は次の意味を有する。
○……透明性良好
△……透明性若干劣る
×……透明性劣る
「アバタ発生」
ロール状物から切り出したフイルムの表面のア
バタ発生を目視で観察した。第1表で示した評価
結果は、次の意味を有する。
○……表面は極めて平滑である
△……表面に若干のアバタ状が認められる
×……表面にかなりのアバタ状が認められる
「シワ発生」
ロール巻状物を巻き戻し、フイルム表面にシワ
入りの有無を目視で観察した。
○……シワは入りは認められない
△……若干シワ入りが認められる
×……かなりのシワ入りが認められる
「フシ発生」
ロール巻状物の巻の上から目視で観察し、色目
の均一度及びフシの発生有無を評価した。第1表
に示した評価結果は次の意味を有する。
○……表面の光沢、色調は均一であり、フシの発
生は認められない
△……表面が黒つぽく見える部分と白つぽく見え
る部分が若干ある
×……表面が黒つぽく見える部分と白つぽく見え
る部分があり、フシの発生が認められる
「レイフラツト性」
ロール巻状物を巻き戻し、フイルム表面の波打
ちの有無を目視で観察した。
○……波打ちは認められない
△……若干波打ちが認められる
×……波打ちがかなり多い
「打痕発生……巻き硬さ」
2個の△状の木材の上にロール巻きを2週間放
置し、木材と接触部分のフイルムの凹みを目視で
観察した。
○……凹みはほとんど認められない
△……若干凹みが認められる
×……かなり凹みが認められる
"Industrial Application Field" The present invention relates to a method for producing a soft vinyl chloride film with improved adhesiveness and surface appearance. In more detail, conventional anti-adhesive powders are sprinkled on the film surface to improve adhesion, which causes the anti-adhesive powder to sink into the film surface, reduce transparency, create avatar-like shapes, and roll-like objects. The present invention relates to a method for producing a soft vinyl chloride resin film with improved adhesion and surface appearance, with improved wrinkles and edges. ``Prior art'' Soft vinyl chloride resin films, which are made by blending a large amount of plasticizer with vinyl chloride resin, are generally produced continuously by calendar molding or extrusion molding, and the film is wound into a roll. It will be done. Soft vinyl chloride resin film is used for daily miscellaneous goods,
It has a wide range of uses, including packaging for clothing and covering agricultural greenhouses. In general, the rolled material is subjected to so-called secondary processing such as unwinding, cutting, welding, and printing, depending on the intended use. Add plasticizer to 100 parts by weight of vinyl chloride resin.
A soft vinyl chloride resin film made by blending 25 parts by weight or more has a high surface smoothness and good transparency, but the film surface is sticky and the film surfaces do not stick together when rolled. are attached to each other. Rolled films whose surfaces adhere to each other in this way are difficult to unwind during secondary processing, resulting in extremely poor workability and, in some cases, resulting in poor product quality. The surfaces of the products may adhere to each other, resulting in defective products. As a method to eliminate such problems, a soft vinyl chloride resin film is continuously produced by a calendar molding method or an extrusion molding method, and immediately before being wound into a roll, starch,
A method of dispersing anti-adhesion fine powder such as talc has been proposed and put into practical use. "Problems to be Solved by the Invention" Generally, a soft vinyl chloride resin film is manufactured continuously by a calendar molding method or an extrusion molding method, and an anti-adhesion fine powder is sprinkled just before it is wound into a roll. In this method, the film temperature is not sufficiently cooled, so the dispersed anti-adhesive powder such as starch and talc sinks into the film surface, resulting in a satin-like film surface that does not lose its smoothness and deteriorates transparency. There was a trend. In order to solve the above problem, we lowered the temperature of the film during winding. As a result, wrinkles appeared on the wound film, and the rolled film had undulations (unevenness) called wrinkles. )
There was a tendency for this to occur. In addition, if the film is produced continuously using a calendar molding method or an extrusion molding method, and an anti-adhesion fine powder is sprinkled just before winding it into a roll, the surface of the film becomes slippery, so air is drawn in. There was a tendency for the rolled film to become avatar-like, resulting in poor appearance, and for the rolled film to become loose, causing dents to occur when the rolled film was transported or stored. "Means for Solving the Problems" The inventors of the present invention have found that in such a situation, the anti-blocking agent sinks into the film surface and air gets entangled without losing the smoothness and transparency of the surface of the soft vinyl chloride resin film. Soft vinyl chloride that does not cause avatar-like formations, does not cause creases, wrinkles, or wrinkles on rolls, is hard to roll, does not leave dents, and has good adhesiveness and surface appearance. The present invention has been completed as a result of extensive research aimed at providing a method for producing a resin film. Therefore, the gist of the present invention is to form a resin composition containing 100 parts by weight of a vinyl chloride resin and 25 to 100 parts by weight of a plasticizer into a film by a calendar molding method or an extrusion molding method, and then wind it into a roll. , cool and later unwind this roll spool;
The present invention provides a method for producing a soft vinyl chloride resin film with good tack and surface appearance, which comprises scattering anti-adhesion fine powder on at least one side of the film and then winding the film. The present invention will be explained in detail below. In the present invention, the vinyl chloride resin refers to polyvinyl chloride and a copolymer mainly composed of vinyl chloride. Monomers copolymerizable with vinyl chloride include vinyl esters, vinyl ethers, acrylic acid or methacrylic acid and their esters, maleic acid or fumaric acid and their esters, maleic anhydride, aromatic acid vinyl compounds, Vinylidene halide compounds, acrylonitrile, methachronitrile,
Examples include ethylene and propylene. To soften the above vinyl chloride resin, resin
25 to 100 parts by weight of plasticizer is added to 100 parts by weight. Examples of plasticizers that can be used include phthalate esters such as dioctyl phthalate, dibutyl phthalate, butylbenzyl phthalate, dibenzyl phthalate, diisodecyl phthalate, didodecyl phthalate, and diudecyl phthalate; dioctyl adipate, n-butyl adipate, Aliphatic dibasic acid esters such as dibutyl sebacate; glycol esters such as pentaerythritol ester and diethylene glycol benzoate; fatty acid esters such as methyl acetyl ricinoleate; phosphate esters such as tricresyl phosphate and tricylenyl phosphate Class; epoxidized soybean oil,
Epoxy compounds such as epoxidized linseed oil and diglycidyl bisphenol A; citric acid esters such as acetyl tributyl citrate, acetyl trioctyl citrate, tri-n-butyl citrate, trialkyl trimellitate, tetra-n-
Examples include plasticizers with various structures such as octyl pyromellitate, polypropylene adipate, and other polyester-based plasticizers. In addition to the above-mentioned plasticizers, the vinyl chloride resin may contain various usual resin additives as necessary, such as stabilizers, lubricants, antifogging agents, antistatic agents, antioxidants, ultraviolet absorbers, light stabilizers, Dyes, pigments, fillers, flame retardants, etc. can be blended. These resin additives can be selected in the usual amount, for example, within the range of 10 parts by weight or less per 100 parts by weight of the base vinyl chloride resin. To blend the vinyl chloride resin plasticizer and various resin additives, use conventional mixing and blending techniques such as a ribbon blender, Banbury mixer, super mixer, and other conventionally known blenders and mixers. good. In the method of the present invention, the vinyl chloride resin composition containing the plasticizer is formed into a film. To form a film from the vinyl chloride resin composition,
Extrusion molding methods such as T-die method and inflation method,
and calendar molding techniques are adopted. The film is formed into a film having a desired width and a desired thickness in the range of 0.03 mm to 1 mm, and is then wound up into a roll. The winding method may be any conventionally known method;
For example, it is wound up using a center winder, a surf-swinder, etc. to form a roll-shaped product. The winding temperature at this time may be a temperature that does not cause wrinkles, but preferably 20°C to 60°C. If the winding temperature is lower than 20°C, wrinkles tend to occur during winding, which is not preferable. Further, it is not preferable to set the winding temperature higher than 60°C because the film becomes difficult to unwind. In the method of the present invention, each portion of the film wound into a roll is uniformly cooled and solidified, and then unwound, an anti-adhesive fine powder is sprinkled on at least one side of the film, and the film is wound again into a roll. The anti-adhesive fine powder used in the method of the present invention may be any of those conventionally used as anti-adhesive powders, such as starch fine powder obtained from plants such as potatoes, corn, and wheat, talc, tetrasilicon mica, etc. The fine starch powder, talc, and tetrasilicon mica mentioned above are hygroscopic, so if a film with these sprinkled on the surface is stored for a long time, the particles will absorb moisture and coagulate, preventing the films from sticking together. function may deteriorate. In order to prevent or suppress the deterioration of the anti-adhesive function due to changes over time, it is preferable to use fine starch powder whose surface is coated with another substance in advance. Preferred substances for coating the particle surfaces of fine starch powder, talc, and tetrasilicon mica include silicone oil and fluorine compounds. A specific example of silicone oil is a silicone oil with a skeleton of siloxane bonds and a silicon atom containing a methyl group, phenyl group, hydroxyl group, etc.
Examples include dimethylpolysiloxane, diphenylpolysiloxane, methylphenylpolysiloxane, dimethyl-methylphenylpolysiloxane, dimethyl-diphenylpolysiloxane, and methylhydrogenpolysiloxane. Examples of fluorine-based compounds include tetrafluoroethylene resin oligomers,
Examples include fluorine-based compounds containing a perfluoroalkyl group having a functional group such as acrylate or methacrylate at the end. In order to coat the surface of particles such as fine starch powder, talc, tetrasilicon mica, etc. with the above substance, the silicone oil, fluorine-based compound, etc. mentioned above is dispersed or dissolved in a solvent, and the fine starch powder is added and mixed. ,
All you have to do is volatilize the solvent. According to the present invention, the anti-adhesive fine powder such as starch fine powder, talc, tetrasilicon mica, etc. is sprinkled on at least one side of the film surface, and once a vinyl chloride resin film formed by a calender series or an extrusion series is made into a long film. The film is wound into a wide roll, cooled and solidified so that the temperature of each part of the film is uniform, and then the roll-shaped film is rewound and the static electricity on the film surface is removed by a static electricity removal device. The temperature of the film when unwinding the roll-shaped film is determined by the fact that fine anti-adhesive powders such as fine starch powder, talc, and tetrasilicon mica sink into the surface of the film.
The temperature may be any temperature at which the anti-adhesive fine powder does not create dents in the film or adhere to the film, and although it varies depending on the amount of plasticizer contained in the film, it is preferably 10°C to 30°C. If the film temperature is lower than 10° C., the film loses its flexibility and tends to cause problems such as tearing when trimming both ends, which is not preferable. Further, if the film temperature is higher than 30°C, the film surface becomes soft, the anti-tack agent sinks into the film or adheres to the film, the film has a satin-like appearance, and the transparency deteriorates, which is undesirable. Further, the particle size of the fine starch powder, talc, tetrasilicon mica, etc. used in the present invention is preferably in the range of 1 to 30 microns. If the average particle diameter is less than 1 micron, the particles may aggregate and fall onto the film surface in large clumps called droplets, which is undesirable since the film surface may lose its smoothness. Also, if the average particle size is larger than 30 microns,
When the film is wound into a roll, a large amount of air is trapped between the films, making it difficult to form a tight roll, and problems such as dents may occur during transport or storage of the roll, which is undesirable. Spraying anti-blocking agents such as fine starch powder, talc, and tetrasilicon mica onto the film surface uses conventionally known equipment such as an electrostatic duster that uses static electricity to charge particles and a spray machine that uses a rotating drum. It depends on the method used. The amount of spraying on the film surface can be selected depending on the type of plasticizer mixed in the film, the amount of plasticizer mixed, the secondary processing method of the film, etc., and is in the range of 0.01 to 5 grams per square meter of film. It is preferable to do so. If the amount of spraying is less than 0.01g/ m2 , the anti-adhesive effect on the film surface will be reduced,
If the amount is more than m 2 , the film may slip too much, making it impossible to form a sufficiently hard roll, or causing trouble during secondary processing, which is undesirable. "Effects of the Invention" A soft vinyl chloride resin film produced by the calendar molding method or extrusion molding method as described above is wound into a long and wide roll, uniformly cooled and solidified, and then unwound. This film is made by scattering anti-adhesive fine powder on at least one side of the film and rewinding it into a roll. In comparison with a film sprinkled with a fine powder to prevent film adhesion, the following effects are particularly remarkable, and its industrial value is extremely great. (1) The soft vinyl chloride resin film obtained by the present invention has good film smoothness because the anti-adhesion fine powder does not sink into the soft vinyl chloride resin film or stick to the film surface.
Transparency is also extremely good. (2) According to the method of the present invention, the anti-adhesive powder does not sink into the film and does not stick to the film surface, so compared to the conventional method, the anti-adhesive effect is produced by dispersing a small amount of the anti-adhesive powder, so it is economical. It is both practical and hygienic, and can prevent the negative effects of anti-adhesion fine powder on products after secondary processing. (3) According to the present invention, the anti-adhesive fine powder does not sink into the film or stick to the film surface, so even if a special anti-adhesive effect is required and a large amount of anti-adhesive fine powder is sprinkled, the film will remain intact. There is no adverse effect on the surface appearance. (4) According to the present invention, a film with good surface smoothness and transparency can be obtained without causing avatar-like appearance defects due to air being trapped between the rolled films. (5) According to the present invention, the film on which the anti-adhesion fine powder is sprinkled is uniformly cooled and solidified, so compared to the conventional method, the film is less likely to be distorted even when wound with a large tension, and the film is rolled with a hard roll. Since a roll is obtained, dents (dents) that occur during transport and storage of the roll are less likely to occur, and the surface appearance of the film is not impaired. (6) According to the present invention, since each part of the film is uniformly cooled and solidified, it is possible to obtain a film with a good surface appearance and no wrinkles (involvement wrinkles) compared to conventional methods. (7) According to the present invention, since the anti-adhesion fine powder is uniformly dispersed on the surface of the film that has been cooled and solidified and is then wound up into a roll, there is almost no shrinkage of the film after rolling, and the film rolls due to thick and thin parts. There is no formation of edges (unevenness) in the rolled material.
The uniform cylindrical shape of the rolled material is maintained, and the smoothness (lay flatness) when the film is unwound from the rolled material is good. Hereinafter, the present invention will be explained in detail based on Examples and Comparative Examples, but the present invention is not limited to the following examples unless it exceeds the gist thereof. Example 1 Polyvinyl chloride (=1100) 100 parts by weight dioctyl phthalate As shown in Table 1, raw materials and resin additives consisting of barium-zinc composite stabilizer 2 parts by weight epoxidized soybean oil 3 were weighed. After stirring and mixing these in a super mixer for 10 minutes,
The mixture was kneaded on rolls heated to 0.degree. C. and rolled into a transparent soft vinyl chloride film with a width of 1000 mm and a thickness of 0.1 m/m using an inverted L-shaped calender. This film is heated to 45℃ using a cooling device.
After being cooled to a temperature of 1,000 m, it was wound into a roll with a length of 1000 m using a winder. The above roll was left to stand for 24 hours, the film was unwound from the roll at a film temperature of 20°C, and fine starch powder ( 0.1 g of AS-100 (manufactured by Nitsuka Corporation, average particle diameter 15 microns) per 1 square meter of film was applied, and after cutting both ends of the film, it was wound into a roll having a width of 970 mm and a winding length of 100 m. Examples 2 to 17 The type of anti-blocking agent in Example 1, the amount of spraying, the blending amount of plasticizer for the fabric, the temperature for winding the fabric, and the film temperature during spraying of the anti-blocking agent were changed as shown in Table 1. Other than that, 16 types of rolls were manufactured in the same manner as in Example 1. Comparative Examples 1 to 6 The same polyvinyl chloride resin composition as in Example 1 was mixed and kneaded in the same manner as in Example 1, and was heated to a width of 1000 m/m and a thickness of 0.1 using an inverted L calender.
It was rolled into a transparent soft vinyl chloride film of m/m. The film after it comes out of the calendar roll,
The film was brought into contact with a cooling roll to cool the film to the various temperatures shown in Table 1, and various fine powders shown in Table 1 were sprayed at the amounts shown in Table 1. Put this film in a winder
It was wound into a roll 100m long. Rolls of 23 types of soft vinyl chloride resin films produced in Examples and Comparative Examples were heated at a temperature of 25°C and a relative humidity of 90%.
After leaving the film for two weeks in an atmosphere of carried out. The evaluation results shown in Table 1 have the following meanings. "Film tackiness" ○... Almost no tackiness △... Slight tackiness ×... Significant tackiness "Surface smoothness" Observe with the naked eye the surface of the film that was evaluated for tackiness above. did. The evaluation results shown in Table 1 have the following meanings. ○...Surface is extremely smooth △...Slight unevenness is observed on the surface due to powder penetration ×..."Transparency" where considerable unevenness is observed on the surface due to powder penetration and adhesion Film cut from a roll-shaped material was held up to a light source and its transparency was judged visually. The evaluation results shown in Table 1 have the following meanings. ○...Good transparency △...Slightly poor transparency ×...Poor transparency "Avatar generation" The appearance of avatars on the surface of the film cut out from the roll was visually observed. The evaluation results shown in Table 1 have the following meanings. ○...Surface is extremely smooth △...Slight avatar-like appearance is observed on the surface ×...Significant avatar-like appearance is observed on the surface ``Wrinkle generation'' When the rolled material is rewound, wrinkles appear on the film surface. The presence or absence of was visually observed. ○...No wrinkles are observed △...Some wrinkles are observed ×...Severe wrinkles are observed "Furrying" Visually observe from the top of the roll to check the uniformity of the color. The occurrence or non-occurrence of snails was evaluated. The evaluation results shown in Table 1 have the following meanings. ○...The gloss and color tone of the surface are uniform, and there are no spots observed.△...There are some areas where the surface looks black and some areas where it looks white.×...There are some areas where the surface looks black and white. "Lay flat property" where there are white spots and formation of wrinkles is observed.The rolled material was rewound and the presence or absence of waviness on the film surface was visually observed. ○... No waving △... Slight waving ×... Quite a lot of waving ``Hatting occurred...Rolling hardness'' Rolls were left on two △-shaped pieces of wood for two weeks. The dents in the film at the parts that came into contact with the wood were visually observed. ○...Almost no dents are observed △...Some dents are observed ×...Significant dents are observed
【表】【table】
Claims (1)
100重量部を含む樹脂組成物をカレンダー成形法
又は押出成形法によりフイルム化し、ロール巻状
に巻き取り、冷却し、後にこのロール巻状物を巻
き戻し、少なくともフイルムの片面に粘着防止微
粉末を散布して巻き取ることを特徴とする粘着性
及び表面外観良好な軟質塩化ビニル系樹脂フイル
ムの製造方法。 2 樹脂組成物をカレンダー成形法又は押出成形
法によりフイルム化した際の巻き取り温度が20℃
〜60℃であることを特徴とする特許請求の範囲第
1項記載の粘着性及び表面外観良好な軟質塩化ビ
ニル系樹脂フイルムの製造方法。 3 冷却したロール巻状物を巻戻す時のフイルム
の温度が10〜30℃であることを特徴とする特許請
求の範囲第1項記載の粘着性及び表面外観の良好
な軟質塩化ビニル系樹脂フイルムの製造方法。 4 粘着防止微粉末がシリコンオイル、フツ素化
合物によつて表面処理されたデンプン微粉末又は
四ケイ素雲母であることを特徴とする特許請求の
範囲第1項記載の粘着性及び表面外観の良好な軟
質塩化ビニル系樹脂フイルムの製造方法。 5 粘着防止微粉末の平均粒子径が1〜30ミクロ
ンであり、フイルム1m2当りの散布量が0.01〜5
gであることを特徴とする特許請求の範囲第1項
又は第4項記載の粘着性及び表面外観の良好な軟
質塩化ビニル系樹脂フイルムの製造方法。[Claims] 1. 100 parts by weight of vinyl chloride resin and 25 to 25 parts by weight of plasticizer
A resin composition containing 100 parts by weight is formed into a film by calender molding or extrusion molding, wound into a roll, cooled, and then unwound and coated with anti-adhesion fine powder on at least one side of the film. A method for producing a soft vinyl chloride resin film with good adhesiveness and good surface appearance, which comprises spraying and winding. 2 The winding temperature when the resin composition is made into a film by calendar molding or extrusion molding is 20°C.
A method for producing a soft vinyl chloride resin film with good tackiness and good surface appearance according to claim 1, wherein the temperature is 60°C. 3. A soft vinyl chloride resin film with good adhesiveness and surface appearance according to claim 1, characterized in that the temperature of the film when unwinding the cooled roll is 10 to 30°C. manufacturing method. 4. Good adhesion and surface appearance as set forth in claim 1, wherein the anti-adhesion fine powder is silicone oil, starch fine powder surface-treated with a fluorine compound, or tetrasilicon mica. A method for producing a soft vinyl chloride resin film. 5. The average particle diameter of the anti-adhesion fine powder is 1 to 30 microns, and the amount of spraying per 1 m2 of film is 0.01 to 5.
5. A method for producing a flexible vinyl chloride resin film with good adhesiveness and surface appearance according to claim 1 or 4, characterized in that: g.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61146561A JPS633932A (en) | 1986-06-23 | 1986-06-23 | Manufacture of soft vinyl chloride resin film with favorable tackiness and surface appearance |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61146561A JPS633932A (en) | 1986-06-23 | 1986-06-23 | Manufacture of soft vinyl chloride resin film with favorable tackiness and surface appearance |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS633932A JPS633932A (en) | 1988-01-08 |
JPH0562571B2 true JPH0562571B2 (en) | 1993-09-08 |
Family
ID=15410457
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61146561A Granted JPS633932A (en) | 1986-06-23 | 1986-06-23 | Manufacture of soft vinyl chloride resin film with favorable tackiness and surface appearance |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS633932A (en) |
-
1986
- 1986-06-23 JP JP61146561A patent/JPS633932A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS633932A (en) | 1988-01-08 |
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EXPY | Cancellation because of completion of term |