JP2555266B2 - Resin composition - Google Patents
Resin compositionInfo
- Publication number
- JP2555266B2 JP2555266B2 JP5291824A JP29182493A JP2555266B2 JP 2555266 B2 JP2555266 B2 JP 2555266B2 JP 5291824 A JP5291824 A JP 5291824A JP 29182493 A JP29182493 A JP 29182493A JP 2555266 B2 JP2555266 B2 JP 2555266B2
- Authority
- JP
- Japan
- Prior art keywords
- evoh
- resin
- composition
- compatibility
- present
- 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
- 239000011342 resin composition Substances 0.000 title claims description 5
- 229920006122 polyamide resin Polymers 0.000 claims description 20
- -1 fatty acid salt Chemical class 0.000 claims description 12
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 11
- 229930195729 fatty acid Natural products 0.000 claims description 11
- 239000000194 fatty acid Substances 0.000 claims description 11
- 229920005989 resin Polymers 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 238000002156 mixing Methods 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 6
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 5
- 230000000737 periodic effect Effects 0.000 claims description 5
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 5
- 238000007127 saponification reaction Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 description 36
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 27
- UFRKOOWSQGXVKV-UHFFFAOYSA-N ethene;ethenol Chemical compound C=C.OC=C UFRKOOWSQGXVKV-UHFFFAOYSA-N 0.000 description 27
- 239000004715 ethylene vinyl alcohol Substances 0.000 description 27
- 239000010410 layer Substances 0.000 description 12
- 238000000465 moulding Methods 0.000 description 12
- 230000000694 effects Effects 0.000 description 10
- 239000007789 gas Substances 0.000 description 10
- 230000004888 barrier function Effects 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 9
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 238000001125 extrusion Methods 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 229920002647 polyamide Polymers 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 5
- 229920005992 thermoplastic resin Polymers 0.000 description 5
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 description 4
- 230000001771 impaired effect Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229920002302 Nylon 6,6 Polymers 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XHALKWMTKWHQLO-UHFFFAOYSA-N 2-tert-butyl-4-(3-tert-butyl-4-hydroxyphenyl)sulfanylphenol Chemical compound C1=C(O)C(C(C)(C)C)=CC(SC=2C=C(C(O)=CC=2)C(C)(C)C)=C1 XHALKWMTKWHQLO-UHFFFAOYSA-N 0.000 description 2
- UFFRSDWQMJYQNE-UHFFFAOYSA-N 6-azaniumylhexylazanium;hexanedioate Chemical compound [NH3+]CCCCCC[NH3+].[O-]C(=O)CCCCC([O-])=O UFFRSDWQMJYQNE-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- 229920000305 Nylon 6,10 Polymers 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- HIAAVKYLDRCDFQ-UHFFFAOYSA-L calcium;dodecanoate Chemical compound [Ca+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O HIAAVKYLDRCDFQ-UHFFFAOYSA-L 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 150000001875 compounds Chemical class 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
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- MEZZCSHVIGVWFI-UHFFFAOYSA-N 2,2'-Dihydroxy-4-methoxybenzophenone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1O MEZZCSHVIGVWFI-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- WZUNUACWCJJERC-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CC)(CO)CO WZUNUACWCJJERC-UHFFFAOYSA-N 0.000 description 1
- JZODKRWQWUWGCD-UHFFFAOYSA-N 2,5-di-tert-butylbenzene-1,4-diol Chemical compound CC(C)(C)C1=CC(O)=C(C(C)(C)C)C=C1O JZODKRWQWUWGCD-UHFFFAOYSA-N 0.000 description 1
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
- XDOLZJYETYVRKV-UHFFFAOYSA-N 7-Aminoheptanoic acid Chemical compound NCCCCCCC(O)=O XDOLZJYETYVRKV-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 229920003189 Nylon 4,6 Polymers 0.000 description 1
- 229920000577 Nylon 6/66 Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- IRSIXPIXVUHQHC-UHFFFAOYSA-N azane;ethene;hexanedioic acid Chemical compound N.N.C=C.OC(=O)CCCCC(O)=O IRSIXPIXVUHQHC-UHFFFAOYSA-N 0.000 description 1
- TZYHIGCKINZLPD-UHFFFAOYSA-N azepan-2-one;hexane-1,6-diamine;hexanedioic acid Chemical compound NCCCCCCN.O=C1CCCCCN1.OC(=O)CCCCC(O)=O TZYHIGCKINZLPD-UHFFFAOYSA-N 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 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 1
- 238000000071 blow moulding Methods 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 238000009820 dry lamination Methods 0.000 description 1
- IAJNXBNRYMEYAZ-UHFFFAOYSA-N ethyl 2-cyano-3,3-diphenylprop-2-enoate Chemical compound C=1C=CC=CC=1C(=C(C#N)C(=O)OCC)C1=CC=CC=C1 IAJNXBNRYMEYAZ-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 1
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-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
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- 150000002888 oleic acid derivatives Chemical class 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000232 polyglycine polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229940031953 sorbitan monopalmitate Drugs 0.000 description 1
- 235000011071 sorbitan monopalmitate Nutrition 0.000 description 1
- 239000001570 sorbitan monopalmitate Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、ポリアミド系樹脂とエ
チレン−酢酸ビニル共重合体鹸化物との相溶性が著しく
改善された組成物に関する。FIELD OF THE INVENTION The present invention relates to a composition in which the compatibility between a polyamide resin and a saponified ethylene-vinyl acetate copolymer is remarkably improved.
【0002】[0002]
【従来の技術】エチレン−酢酸ビニル共重合体鹸化物
(以下、EVOHと省略することがある)とポリアミド
系樹脂のブレンド組成物は特徴のある物性を備えてい
る。殊に、各種熱可塑性樹脂とEVOHの多層共押出成
形時に、熱可塑性樹脂層あるいはEVOH層に代えて、
前記ブレンド組成物を使用したり、あるいは熱可塑性樹
脂とEVOH層の中間に前記ブレンド組成物の層を設け
ることによって層間接着力を向上させることができる。
また、前記ブレンド組成物単独を溶融押出成形し、さら
に必要に応じて延伸および/あるいは熱処理して得られ
たフィルム、シートあるいはボトルなどの成形物は気体
遮断性と力学的物性に優れている。このようにポリアミ
ド系樹脂とEVOHのブレンド組成物の特徴は従来も知
られていたが、この組成物は相溶性が良好とはいえず、
押出成形によりフィルム、シート、ボトルなどを成形す
ると、不均一な相分離異物を生じやすく、特に長時間の
運転によりこの異物が増加して外観を著しく損ねること
が知られている。こうして、ポリアミド系樹脂とEVO
Hのブレンド組成物は、その優れた特徴にもかかわらず
押出成形が実用的に全く実施できないか、できても短時
間しか運転できないのが実情であった。2. Description of the Related Art A blend composition of a saponified ethylene-vinyl acetate copolymer (hereinafter sometimes abbreviated as EVOH) and a polyamide resin has characteristic physical properties. In particular, in the multi-layer coextrusion molding of various thermoplastic resins and EVOH, instead of the thermoplastic resin layer or EVOH layer,
The interlayer adhesion can be improved by using the blend composition or by providing a layer of the blend composition between the thermoplastic resin and the EVOH layer.
Further, a molded product such as a film, a sheet or a bottle obtained by subjecting the blend composition alone to melt extrusion molding and further stretching and / or heat-treating as necessary has excellent gas barrier properties and mechanical properties. As described above, the characteristics of the blend composition of the polyamide-based resin and EVOH have been known so far, but this composition cannot be said to have good compatibility,
It is known that when a film, a sheet, a bottle or the like is molded by extrusion molding, a non-uniform phase-separated foreign substance is likely to be generated, and the foreign substance is increased and the appearance is significantly impaired especially when operated for a long time. Thus, polyamide resin and EVO
Despite the excellent characteristics of the H blend composition, extruding cannot be practically performed at all, or it can be operated only for a short time if possible.
【0003】[0003]
【発明が解決しようとする課題】本発明は、このような
相溶性不良を解消するためになされたものであり、外観
美麗な成形物を得ることを目的とする。SUMMARY OF THE INVENTION The present invention has been made in order to eliminate such poor compatibility, and an object of the present invention is to obtain a molded article having a beautiful appearance.
【0004】[0004]
【課題を解決するための手段】上記目的は、(A)ポリ
アミド系樹脂、(B)エチレン単位20〜50モル%、
酢酸ビニル単位の鹸化度96%以上のエチレン−酢酸ビ
ニル共重合体鹸化物および(C)周期律表I族、II族お
よびIII族から選ばれる少なくとも1種の金属の脂肪酸
塩からなり、かつ上記樹脂(A)と上記樹脂(B)との
配合割合が60:40〜99.9:0.1(重量比)で
あり、上記成分(C)を上記樹脂(A)と(B)の重量
の和100部に対し0.00001〜10部含有する樹
脂組成物を提供することによって達成される。この組成
物を用いて成形した場合にはポリアミド系樹脂とEVO
Hの相溶性が顕著に改善され、外観が美しく、かつ層間
接着力の高い共押し出し成形品、あるいは気体遮断性と
力学的物性に優れた成形物が得られる。The above-mentioned objects are (A) poly
Amide resin, (B) ethylene unit 20 to 50 mol%,
Ethylene-vinyl acetate with a degree of saponification of vinyl acetate units of 96% or more
Saponified nyl copolymer and (C) Group I and II of the periodic table
And fatty acids of at least one metal selected from Group III
Consisting of salt and containing the resin (A) and the resin (B)
Mixing ratio is 60: 40-99.9: 0.1 (weight ratio)
Yes, the above component (C) is the weight of the above resins (A) and (B)
Tree containing 0.00001 to 10 parts per 100 parts of sum
This is accomplished by providing a fat composition. When molded using this composition, a polyamide resin and EVO
The compatibility of H is remarkably improved, and a coextruded product having a beautiful appearance and high interlaminar adhesive strength, or a molded product having excellent gas barrier properties and mechanical properties can be obtained.
【0005】本発明においてポリアミド系樹脂として
は、ポリカプラミド(ナイロン−6)、ポリ−ω−アミ
ノヘプタン酸(ナイロン−7)、ポリ−ω−アミノノナ
ン酸(ナイロン−9)、ポリウンデカンアミド(ナイロ
ン−11)、ポリラウリンラクタム(ナイロン−1
2)、ポリエチレンジアミンアジパミド(ナイロン−
2,6)、ポリテトラメチレンアジパミド(ナイロン−
4,6)、ポリヘキサメチレンアジパミド(ナイロン−
6,6)、ポリヘキサメチレンセバカミド(ナイロン−
6,10)、ポリヘキサメチレンドデカミド(ナイロン
−6,12)、ポリオクタメチレンアジパミド(ナイロ
ン−8,6)、ポリデカメチレンアジパミド(ナイロン
−10,6)、ポリデカメチレンセバカミド(ナイロン
−10,8)、あるいは、カプロラクタム/ラウリンラ
クタム共重合体、カプロラクタム/ヘキサメチレンジア
ンモニウムアジペート共重合体、ラウリンラクタム/ヘ
キサメチレンジアンモニウムアジペート共重合体、ヘキ
サメチレンジアンモニウムアジペート/ヘキサメチレン
ジアンモニウムセバケート共重合体、エチレンジアンモ
ニウムアジペート/ヘキサメチレンジアンモニウムアジ
ペート共重合体、カプロラクタム/ヘキサメチレンジア
ンモニウムアジペート/ヘキサメチレンジアンモニウム
セバケート共重合体、などが挙げられる。このなかでは
カプロラクタム/ヘキサメチレンジアンモニウムアジペ
ート共重合体(ナイロン−6/66)が、EVOHとの
ブレンド物の物性がとりわけ優れており、実用的に特に
重要である。In the present invention, as the polyamide resin, polycapramide (nylon-6), poly-ω-aminoheptanoic acid (nylon-7), poly-ω-aminononanoic acid (nylon-9), polyundecane amide (nylon-). 11), polylaurinlactam (nylon-1)
2), polyethylenediamine adipamide (nylon-
2, 6), polytetramethylene adipamide (nylon-
4, 6), polyhexamethylene adipamide (nylon-
6, 6), polyhexamethylene sebacamide (nylon-
6, 10), polyhexamethylene dodecamide (nylon-6,12), polyoctamethylene adipamide (nylon-8,6), polydecamethylene adipamide (nylon-10,6), polydecamethylenese Bacamide (nylon-10,8) or caprolactam / laurinlactam copolymer, caprolactam / hexamethylene diammonium adipate copolymer, laurin lactam / hexamethylene diammonium adipate copolymer, hexamethylene diammonium adipate / hexa Methylene diammonium sebacate copolymer, ethylene diammonium adipate / hexamethylene diammonium adipate copolymer, caprolactam / hexamethylene diammonium adipate / hexamethylene diammonium sebacate copolymer , And the like. Among them, a caprolactam / hexamethylenediammonium adipate copolymer (nylon-6 / 66) is particularly excellent in physical properties of a blend with EVOH, and is particularly important in practical use.
【0006】また、本発明にいうエチレン−酢酸ビニル
共重合体鹸化物(EVOH)(B)とはエチレンと酢酸
ビニルの共重合体中の酢酸ビニル単位を加水分解したも
のであれば任意のものを含むものであるが、ポリアミド
系樹脂との相溶性が不良であるものは比較的エチレン単
位が少なく酢酸ビニル単位の鹸化度(加水分解度)が高
いものである。特に、エチレン単位の含量が20〜50
モル%で、酢酸ビニル単位の鹸化度が96%以上、とり
わけ99%以上のものは酸素などの気体に対する気体遮
断性が熱可塑性樹脂中で最高の水準にあり、かつ、ポリ
オレフィンと複合して用いることにより優れた容器類が
得られることから、本発明の適用対象として特に重要で
ある。[0006] The saponified ethylene-vinyl acetate copolymer (EVOH) (B) referred to in the present invention may be any one obtained by hydrolyzing a vinyl acetate unit in a copolymer of ethylene and vinyl acetate. Those having poor compatibility with the polyamide resin have relatively few ethylene units and high saponification degree (hydrolysis degree) of vinyl acetate units. In particular, the content of ethylene units is 20 to 50.
Mol% having a vinyl acetate unit saponification degree of 96% or more, particularly 99% or more, has the highest gas barrier property against a gas such as oxygen among thermoplastic resins and is used in combination with a polyolefin. As a result, excellent containers can be obtained, which is particularly important as an application target of the present invention.
【0007】更に、本発明の組成物を構成する、周期律
表I族、II族およびIII族から選ばれる少なくとも1種
の金属の脂肪酸塩(C)としては多くの化合物が挙げら
れるが、とりわけマグネシウム、カルシウム、亜鉛など
周期律表II族の金属の脂肪酸塩が特に有効に作用する傾
向が見出されている。脂肪酸の金属(I族、II族あるい
はIII族)塩を構成する脂肪酸としては酢酸、プロピオ
ン酸、酪酸、カプロン酸、カプリル酸、などの低級脂肪
酸、ラウリン酸、ステアリン酸、ミリスチン酸などの高
級脂肪酸が挙げられる。このうち、炭素数が8〜22の
範囲の高級脂肪酸の金属塩、とりわけ、カルシウム塩、
マグネシウム塩、亜鉛塩が本発明の目的に特に好適であ
る。これらの(C)成分は、単独または2種以上混合し
て使用される。Further, as the fatty acid salt (C) of at least one metal selected from Group I, Group II and Group III of the periodic table constituting the composition of the present invention, many compounds can be mentioned. It has been found that fatty acid salts of metals belonging to Group II of the periodic table, such as magnesium, calcium and zinc, tend to work particularly effectively. Fatty acids constituting metal (Group I, Group II or Group III) salts of fatty acids include lower fatty acids such as acetic acid, propionic acid, butyric acid, caproic acid, and caprylic acid; and higher fatty acids such as lauric acid, stearic acid, and myristic acid. Is mentioned. Among these, metal salts of higher fatty acids having 8 to 22 carbon atoms, especially calcium salts,
Magnesium salts and zinc salts are particularly suitable for the purpose of the present invention. These components (C) are used alone or in combination of two or more.
【0008】本発明の組成物を構成するポリアミド系樹
脂(A)とEVOH(B)の組成比はポリアミド系樹脂
(A):EVOH(B)の重量比として60:40〜9
9.9:0.1であり、とりわけ70:30〜99.
7:0.3の範囲のものが好ましい。EVOH(B)が
0.1重量%以下では、ポリアミド系樹脂の気体遮断性
改善の効果が得られず、EVOH(B)が40重量%以
上では、ポリアミド系樹脂の力学的特性、特に強度の低
下が著しい。 Polyamide-based tree constituting the composition of the present invention
The composition ratio of the fat (A) and EVOH (B) is a polyamide resin
(A): EVOH (B) weight ratio 60: 40-9
9.9: 0.1, especially 70: 30-99.
It is preferably in the range of 7: 0.3. EVOH (B)
If less than 0.1% by weight, the gas barrier properties of polyamide resin
The improvement effect cannot be obtained, and EVOH (B) is 40% by weight or less.
Above, the mechanical properties of polyamide-based resin, especially the low strength
The bottom is remarkable.
【0009】また、相溶性を改善する、脂肪酸塩(C)
の添加量は(A)、(B)および(C)成分の種類に応
じて相溶性改良効果が得られ、なおかつ組成物の力学的
物性、透明性、気体遮断性などの諸物性を損なわない範
囲で調整されるが、多くの場合、その量はポリアミド系
樹脂(A)とEVOH(B)の重量の和(A+B)10
0部に対して0.00001〜10部、とりわけ0.0
001〜1部の範囲で用いられる。10部を越えると相
溶性以外の諸物性が損なわれやすく好ましくない場合が
多い。Further, a fatty acid salt (C) for improving the compatibility
Depending on the type of the components (A), (B) and (C), the effect of improving the compatibility can be obtained and the physical properties of the composition such as mechanical properties, transparency and gas barrier properties are not impaired. It is adjusted in the range, but in many cases, the amount is the sum of the weight of the polyamide resin (A) and the EVOH (B) (A + B) 10.
0.00001 to 10 parts, particularly 0.0
It is used in the range of 001 to 1 part. If it exceeds 10 parts, physical properties other than compatibility are likely to be impaired, which is not preferable in many cases.
【0010】また、(C)成分をあらかじめポリアミド
系樹脂および/あるいはEVOHに配合しておく場合に
は使用効果が高い傾向にある。EVOHに配合しておく
例としてはEVOH100部に(C)成分を0.002
〜0.5部配合したものが挙げられる。この配合物0.
5部とポリアミド系樹脂99.5部を添加した組成物の
溶融成形における相溶性改良効果は顕著である。この場
合、ポリアミド系樹脂とEVOHの重量の和100部に
対する(C)成分の量は0.00001〜0.0025
部となる。(C)成分の量が0.00001部より少な
い場合には一般にその効果は小さい。こうして、(C)
成分をEVOHにブレンドした場合にはその添加量は見
かけ上少なくなる場合でも効果は大きいといえる。When the component (C) is previously blended with the polyamide resin and / or EVOH, the use effect tends to be high. As an example of blending in EVOH, the component (C) is added in an amount of 0.002 to 100 parts of EVOH.
~ 0.5 part is included. This formulation 0.
The effect of improving the compatibility in melt molding of a composition containing 5 parts and 99.5 parts of a polyamide resin is remarkable. In this case, the amount of the component (C) is 0.00001 to 0.0025 per 100 parts by weight of the total weight of the polyamide resin and the EVOH.
Department. When the amount of the component (C) is less than 0.00001 parts, the effect is generally small. Thus, (C)
When the components are blended with EVOH, the effect can be said to be large even if the added amount is apparently small.
【0011】本発明の組成物を得るためのブレンド方法
は特別に制限はなく、3者をドライブレンドする方法、
あるいは(C)成分をポリアミド系樹脂またはEVOH
の全部または一部にあらかじめ配合しておき、それをポ
リアミド系樹脂および/またはEVOHに配合して、前
記(A)、(B)および(C)からなる組成物を得る方
法などが目的に応じて任意に選ばれる。一般には、前述
のようなEVOHに配合しておく方法に加えて、ドライ
ブレンドする方法あるいはあらかじめポリアミド系樹脂
に配合しておく方法を組合せることによりとりわけ顕著
に相溶性改良効果を得ることができる。The blending method for obtaining the composition of the present invention is not particularly limited, and a method of dry-blending the three components,
Alternatively, the component (C) is a polyamide resin or EVOH
Is mixed in advance with all or a part of the above, and is mixed with a polyamide resin and / or EVOH to obtain a composition comprising the above (A), (B) and (C). Selected arbitrarily. In general, in addition to the above-described method of blending with EVOH, a particularly remarkable effect of improving the compatibility can be obtained by combining a method of dry blending or a method of blending in advance with a polyamide resin. .
【0012】本発明において、周期律表I族、II族ある
いはIII族の金属の脂肪酸塩(C)が、ポリアミド系樹
脂とEVOHの溶融成形における相溶性をかくも顕著に
向上させる機構は十分明らかではないが、ポリアミド系
樹脂とEVOHの溶融系におけるレオロジー的効果、不
純物の化学的作用などが複雑に組合わさった状態におい
て(C)成分が有効に作用しているものと推定される。In the present invention, the mechanism by which the fatty acid salt (C) of a metal belonging to Group I, II or III of the Periodic Table significantly improves the compatibility of the polyamide resin and EVOH in melt molding is sufficiently clear. However, it is presumed that the component (C) is effectively acting in a state where the rheological effect and the chemical action of impurities in the molten system of the polyamide resin and EVOH are combined in a complicated manner.
【0013】本発明の樹脂組成物に対しては熱可塑性樹
脂に慣用の他の添加剤を配合することができる。このよ
うな添加剤の例としては、酸化防止剤、紫外線吸収剤、
可塑剤、帯電防止剤、滑剤、着色剤、充填剤、あるいは
他の高分子化合物を挙げることができ、これらを本発明
の作用効果が阻害されない範囲内でブレンドすることが
できる。添加剤の具体的な例としては次の様なものが挙
げられる。The resin composition of the present invention may contain other conventional additives in the thermoplastic resin. Examples of such additives include antioxidants, ultraviolet absorbers,
Plasticizers, antistatic agents, lubricants, coloring agents, fillers, and other high molecular compounds can be used, and these can be blended as long as the effects of the present invention are not impaired. Specific examples of the additives include the following.
【0014】酸化防止剤:2,5−ジ−t−ブチルハイ
ドロキノン、2,6−ジ−t−ブチル−p−クレゾー
ル、4,4′−チオビス−(6−t−ブチルフェノー
ル)、2,2′−メチレン−ビス(4−メチル−6−t
−ブチルフェノール)、オクタデシル−3−(3′,
5′−ジ−t−ブチル−4′−ヒドロキシフェニル)プ
ロピオネート、4,4′−チオビス−(6−t−ブチル
フェノール)等。紫外線吸収剤:エチル−2−シアノ−
3,3−ジフェニルアクリレート、2−(2′−ヒドロ
キシ−5′−メチルフェニル)ベンゾトリアゾール、2
−(2′ヒドロキシ−3′−t−ブチル−5′−メチル
フェニル)−5−クロロベンゾトリアール、2−ヒドロ
キシ−4−メトキシベンゾフェノン、2,2′−ジヒド
ロキシ−4−メトキシベンゾフェノン、2−ヒドロキシ
−4−オクトキシベンゾフェノン等。可塑剤:フタル酸
ジメチル、フタル酸ジブチル、フタル酸ジオクチル、ワ
ックス、流動パラフィン、リン酸エステル等。帯電防止
剤:ペンタエリスリットモノステアレート、ソルビタン
モノパルミテート、硫酸化オレイン酸、ポリエチレンオ
キシド、カーボワックス等。滑剤:エチレンビスステア
ロアミド、ブチルステアレート等。着色剤:カーボブラ
ック、フタロシアニン、キナクリドン、インドリン、ア
ゾ系顔料、酸化チタン、ベンガラ等。充填剤:グラスフ
ァイバー、アスベスト、マイカ、バラストナイト、ケイ
酸カルシウム、ケイ酸アルミニウム、炭酸カルシウム
等。Antioxidants: 2,5-di-t-butylhydroquinone, 2,6-di-t-butyl-p-cresol, 4,4'-thiobis- (6-t-butylphenol), 2,2 '-Methylene-bis (4-methyl-6-t
-Butylphenol), octadecyl-3- (3 ',
5'-di-t-butyl-4'-hydroxyphenyl) propionate, 4,4'-thiobis- (6-t-butylphenol) and the like. UV absorber: Ethyl-2-cyano-
3,3-diphenyl acrylate, 2- (2'-hydroxy-5'-methylphenyl) benzotriazole, 2
-(2'hydroxy-3'-tert-butyl-5'-methylphenyl) -5-chlorobenzotrial, 2-hydroxy-4-methoxybenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone, 2- Hydroxy-4-octoxybenzophenone and the like. Plasticizer: dimethyl phthalate, dibutyl phthalate, dioctyl phthalate, wax, liquid paraffin, phosphate ester and the like. Antistatic agents: pentaerythritol monostearate, sorbitan monopalmitate, sulfated oleic acid, polyethylene oxide, carbowax and the like. Lubricants: ethylene bis stearamide, butyl stearate, etc. Coloring agents: carbo black, phthalocyanine, quinacridone, indoline, azo pigments, titanium oxide, red iron oxide and the like. Filler: glass fiber, asbestos, mica, ballastonite, calcium silicate, aluminum silicate, calcium carbonate, etc.
【0015】本発明の組成物を得るための各成分の配合
手段としては、リボンブレンダー、高速ミキサー、コニ
ーダー、ミキシングロール、押出機、インテンシブミキ
サー等が例示される。Examples of the means for compounding the components for obtaining the composition of the present invention include a ribbon blender, a high-speed mixer, a co-kneader, a mixing roll, an extruder, and an intensive mixer.
【0016】本発明の樹脂組成物は、周知の溶融押出成
形機、圧縮成形機、トランスファ成形機、射出成形機、
吹込成形機、熱成形機、回転成形機、ディップ成形機な
どを使用して、フィルム、シート、チューブ、ボトルな
どの任意の成形品に成型することができる。成形に際し
ての押出温度は樹脂の種類、分子量、組成物の配合割合
あるいは押出機の性質などのより適宜選択されるが、多
くの場合170〜350℃の範囲である。The resin composition of the present invention can be prepared by a known melt extrusion molding machine, compression molding machine, transfer molding machine, injection molding machine,
Using a blow molding machine, a thermoforming machine, a rotary molding machine, a dip molding machine, or the like, it can be molded into an arbitrary molded product such as a film, a sheet, a tube, and a bottle. The extrusion temperature during molding is appropriately selected depending on the type and molecular weight of the resin, the compounding ratio of the composition, the properties of the extruder, and the like, but in most cases is in the range of 170 to 350 ° C.
【0017】また、本発明の樹脂組成物は多層材の一層
として使用するとき接着性の点で特異な特長が発揮され
ることは前述したとおりであるが、熱可塑性樹脂層を
P、EVOH層をE、接着性樹脂層をD、本発明の組成
物の層をFとするときE/F/E、F/E/F、F/F
/F(中間層のFはEVOHの含量が多い)、F/D/
E、F/D/E/D/F、P/E/P/F、P/F/D
/E/D/F/P、P/F/D/E/D/Pなどの層構
成をとるとき、層間接着性が高く、相溶性に優れた美麗
な成形物を得ることができる。このような多層成形材に
おいては、本発明のブレンド組成物は多層成形物のスク
ラップで代用することもできる。As described above, when the resin composition of the present invention is used as one layer of a multilayer material, it exhibits a unique feature in terms of adhesiveness. Is E, the adhesive resin layer is D, and the layer of the composition of the present invention is F. E / F / E, F / E / F, F / F
/ F (F in the intermediate layer has a high EVOH content), F / D /
E, F / D / E / D / F, P / E / P / F, P / F / D
When a layer structure such as / E / D / F / P and P / F / D / E / D / P is adopted, a beautiful molded product having high interlayer adhesion and excellent compatibility can be obtained. In such a multilayer molding, the blend composition of the present invention can be replaced with scrap of a multilayer molding.
【0018】多層成形方法としては、一般的にいって樹
脂層の種類に対応する数の押出機を使用し、この押出機
内で溶融された樹脂の流れを重ねあわせた層状態で同時
押出成形するいわゆる共押出成形により実施される。別
の方法として、エキストルージョンコーティング、ドラ
イラミネーションなどの多層成形方法も採用されうる。
また、本発明の組成物の単独成形品、あるいは本発明の
組成物も含む多層成形品を一軸延伸、二軸延伸あるいは
ブロー延伸などの延伸を実施することにより、力学的物
性、気体遮断性などにさらに特長のある物性を有する成
形物を得ることができる。こうして、本発明の組成物で
得られた成形物は、ブレンド組成物が均一で外観が美麗
であるばかりでなく、相溶性が良好で均一であることか
ら強度物性、気体遮断性など多くの優れた特長を有して
おりその工業的意義は大きい。以下、実施例により更に
具体的に説明する。なお、部は重量部を意味している。As a multilayer molding method, generally, a number of extruders corresponding to the type of the resin layer are used, and a flow of the resin melted in the extruder is simultaneously extruded in a superposed layer state. It is performed by so-called coextrusion molding. As another method, a multilayer molding method such as extrusion coating or dry lamination can be adopted.
Further, by performing stretching such as uniaxial stretching, biaxial stretching or blow stretching of a single molded article of the composition of the present invention or a multilayer molded article containing the composition of the present invention, mechanical properties, gas barrier properties, etc. In addition, it is possible to obtain a molded product having more characteristic physical properties. Thus, the molded product obtained from the composition of the present invention not only has a uniform and beautiful appearance of the blend composition, but also has excellent excellent properties such as strength properties and gas barrier properties due to good and uniform compatibility. And its industrial significance is great. Hereinafter, the present invention will be described more specifically by way of examples. Parts mean parts by weight.
【0019】[0019]
【実施例】実施例1 6/66共重合ポリアミド(66成分15%、融点19
8℃)80部、EVOH[エチレン単位の含有量33モ
ル%、鹸化度99.9%、メルトインデックス(190
℃、2160g)1.5g/10分]20部、およびラ
ウリン酸カルシウム0.02部をドライブレンドした
後、直径が40mm、L/D=24、圧縮比3.8のフ
ルフライト型スクリューを有する押出機に仕込み、巾5
50mmのフラットダイを使用して成膜を実施した。成
膜温度は押出機を190°〜240℃、ダイを225℃
とし、厚さが100μのフィルムを引取機にて巻き取
り、6時間の連続運転を実施した。得られたフィルムは
均一、かつ良好な相溶性を示し、相溶不良の相分離異物
は僅かに見られた。得られたフィルムの90mm角の試
験片を二軸延伸試験装置((株)東洋精機製作所製)を
使用して85℃で1分間加温後、5m/minの延伸速
度で縦横ともに3倍に延伸した。延伸は均一に実施さ
れ、この延伸フィルムを木枠に固定して熱風乾燥機中で
110℃で熱処理したところ強度と気体遮断性に優れた
良好なフィルムが得られた。Example 1 6/66 copolymerized polyamide (66 components 15%, melting point 19)
8 ° C.) 80 parts, EVOH [ethylene unit content 33 mol%, saponification degree 99.9%, melt index (190
C., 2160 g) 1.5 g / 10 min] 20 parts, and after dry blending 0.02 part of calcium laurate, extrusion having a diameter of 40 mm, L / D = 24, compression ratio 3.8 full flight type screw Charge the machine, width 5
Film formation was performed using a 50 mm flat die. The film forming temperature is 190 ° to 240 ° C for the extruder and 225 ° C for the die.
The film having a thickness of 100 μm was wound up by a take-up machine, and continuously operated for 6 hours. The obtained film showed uniform and good compatibility, and a little phase-separated foreign matter having poor compatibility was observed. A 90-mm square test piece of the obtained film was heated at 85 ° C. for 1 minute using a biaxial stretching test apparatus (manufactured by Toyo Seiki Seisaku-sho, Ltd.), and then tripled both vertically and horizontally at a stretching speed of 5 m / min. Stretched. Stretching was carried out uniformly, and when this stretched film was fixed to a wooden frame and heat-treated at 110 ° C. in a hot air dryer, a good film having excellent strength and gas barrier properties was obtained.
【0020】比較例1 実施例1において、ラウリン酸カルシウムを混合しない
他は実施例1と同様にしてポリアミドとEVOHの混合
品の製膜を実施した。運転開始後30分頃から実施例1
では見られない不均一な相分離異物が多数観察され、そ
の数は時間経過と共に増大し、得られたフィルムの外観
は極めて不良であった。Comparative Example 1 A film of a mixture of polyamide and EVOH was formed in the same manner as in Example 1 except that calcium laurate was not mixed. Example 1 about 30 minutes after the start of operation
A large number of non-uniform phase-separated foreign matters that could not be observed were observed, the number increased with the passage of time, and the appearance of the obtained film was extremely poor.
【0021】実施例2 実施例1に示した6/66共重合ポリアミド(PA)、
EVOHと各種(C)成分とを第1表に示す割合でドラ
イブレンドした後、実施例1と同様にして押出成膜を実
施した。得られたフィルムの膜面状態の評価を表1に合
わせて示した。Example 2 The 6/66 copolymerized polyamide (PA) shown in Example 1,
After EVOH and various components (C) were dry-blended at the ratios shown in Table 1, extrusion film formation was carried out in the same manner as in Example 1. The evaluation of the film surface state of the obtained film is shown in Table 1.
【0022】[0022]
【表1】 [Table 1]
【0023】注1)膜面状態の評価は次の基準により判
定した。 秀:均一かつ良好な相溶性を示し相分離異物が見られな
い。 優:均一かつ良好な相溶性を示しているが、長時間の成
形において、小さい相分離異物が僅かに見られる。 良:相溶性は良好であるが、一部僅かに相分離異物が見
られる。 可:相溶性に改善効果は見られるが、相分離異物含有量
僅かに見られる。Note 1) The film surface condition was evaluated according to the following criteria. Shu: Shows uniform and good compatibility and shows no phase-separated foreign matter. Excellent: A uniform and good compatibility is shown, but a small amount of phase-separated foreign matter is slightly observed in molding for a long time. Good: The compatibility is good, but some phase-separated foreign matters are slightly observed. Acceptable: The effect of improving compatibility was observed, but the content of phase-separated foreign matters was slightly observed.
【0024】[0024]
【発明の効果】ポリアミド系樹脂とEVOHとの相溶性
が顕著に改善され、さらに得られた成形物は外観が美し
く、気体遮断性も優れている。According to the present invention, the compatibility between the polyamide resin and EVOH is remarkably improved, and the obtained molded product has a beautiful appearance and excellent gas barrier properties.
フロントページの続き (56)参考文献 特開 昭60−23159(JP,A) 特開 昭54−63150(JP,A) 特開 昭53−118449(JP,A) 特開 昭59−20345(JP,A) 特開 昭59−207956(JP,A) 特開 昭54−54167(JP,A) 特開 昭54−100442(JP,A) 特開 昭50−100144(JP,A) 特開 昭52−73984(JP,A) 特開 昭54−87783(JP,A) 特開 昭56−86949(JP,A) 特開 昭52−15544(JP,A) 「新版プラスチック配合剤」阿部嘉長 編(株)大成社刊(S59.1.30)P. 284〜285Continuation of front page (56) Reference JP-A-60-23159 (JP, A) JP-A-54-63150 (JP, A) JP-A-53-118449 (JP, A) JP-A-59-20345 (JP , A) JP 59-207956 (JP, A) JP 54-54167 (JP, A) JP 54-100442 (JP, A) JP 50-100144 (JP, A) JP 52-73984 (JP, A) JP 54-87783 (JP, A) JP 56-86949 (JP, A) JP 52-15544 (JP, A) "New edition plastic compounding agent" Yoshinori Abe Edited by Taiseisha Co., Ltd. (S59. 1.30) P. 284-285
Claims (1)
ン単位20〜50モル%、酢酸ビニル単位の鹸化度96
%以上のエチレン−酢酸ビニル共重合体鹸化物および
(C)周期律表I族、II族およびIII族から選ばれる少
なくとも1種の金属の脂肪酸塩からなり、かつ上記樹脂
(A)と上記樹脂(B)との配合割合が60:40〜9
9.9:0.1(重量比)であり、上記成分(C)を上
記樹脂(A)と(B)の重量の和100部に対し0.0
0001〜10部含有する樹脂組成物。1. A (A) polyamide resin, (B) a saponification degree of 20 to 50 mol% of ethylene units and a vinyl acetate unit of 96.
% Or more of a saponified ethylene-vinyl acetate copolymer and (C) a fatty acid salt of at least one metal selected from Group I, Group II and Group III of the periodic table, and the above resin
The mixing ratio of (A) and the resin (B) is 60: 40-9.
9.9: 0.1 (weight ratio), and the amount of the component (C) is 0.0 based on 100 parts by weight of the resins (A) and (B).
A resin composition containing 0001 to 10 parts.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5291824A JP2555266B2 (en) | 1993-10-01 | 1993-11-22 | Resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5291824A JP2555266B2 (en) | 1993-10-01 | 1993-11-22 | Resin composition |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4237686A Division JPH0651817B2 (en) | 1992-08-12 | 1992-08-12 | Resin composition |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6293066A Division JP2588688B2 (en) | 1994-11-28 | 1994-11-28 | Resin composition |
JP1161696A Division JP2604572B2 (en) | 1996-01-26 | 1996-01-26 | Resin composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH06212038A JPH06212038A (en) | 1994-08-02 |
JP2555266B2 true JP2555266B2 (en) | 1996-11-20 |
Family
ID=17773895
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5291824A Expired - Lifetime JP2555266B2 (en) | 1993-10-01 | 1993-11-22 | Resin composition |
Country Status (1)
Country | Link |
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JP (1) | JP2555266B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JP4642170B2 (en) * | 1999-04-06 | 2011-03-02 | 日本合成化学工業株式会社 | Resin composition and laminate |
CN104072864A (en) * | 2014-05-29 | 2014-10-01 | 安徽海纳川塑业科技有限公司 | Heat-resistant light pipe material |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5418693B2 (en) * | 1974-01-08 | 1979-07-10 | ||
JPS5215544A (en) * | 1975-07-29 | 1977-02-05 | Nippon Synthetic Chem Ind Co Ltd:The | Process for producing molded articles based on flame-retarded resins |
JPS54100442A (en) * | 1978-01-25 | 1979-08-08 | Mitsubishi Petrochem Co Ltd | Self-extinguishing resin composition |
JPS6023159A (en) * | 1983-07-12 | 1985-02-05 | カルプ工業株式会社 | packaging material |
-
1993
- 1993-11-22 JP JP5291824A patent/JP2555266B2/en not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
---|
「新版プラスチック配合剤」阿部嘉長編(株)大成社刊(S59.1.30)P.284〜285 |
Also Published As
Publication number | Publication date |
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JPH06212038A (en) | 1994-08-02 |
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