JP6664336B2 - アミン官能化インターポリマーを含む架橋性ポリマー組成物、それを作製するための方法、及びそれから作製された物品 - Google Patents
アミン官能化インターポリマーを含む架橋性ポリマー組成物、それを作製するための方法、及びそれから作製された物品 Download PDFInfo
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- JP6664336B2 JP6664336B2 JP2016567222A JP2016567222A JP6664336B2 JP 6664336 B2 JP6664336 B2 JP 6664336B2 JP 2016567222 A JP2016567222 A JP 2016567222A JP 2016567222 A JP2016567222 A JP 2016567222A JP 6664336 B2 JP6664336 B2 JP 6664336B2
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- crosslinkable polymer
- ethylene
- functionalized interpolymer
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- 238000000034 method Methods 0.000 title claims description 25
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- 239000004702 low-density polyethylene Substances 0.000 claims description 19
- SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 claims description 14
- YTLYLLTVENPWFT-UPHRSURJSA-N (Z)-3-aminoacrylic acid Chemical compound N\C=C/C(O)=O YTLYLLTVENPWFT-UPHRSURJSA-N 0.000 claims description 13
- -1 2- (t-butylamino) ethyl Chemical group 0.000 claims description 12
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- 125000004432 carbon atom Chemical group C* 0.000 description 7
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- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 6
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- PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 6
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- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 4
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- 229920002799 BoPET Polymers 0.000 description 4
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 4
- 239000005041 Mylar™ Substances 0.000 description 4
- KVOZXXSUSRZIKD-UHFFFAOYSA-N Prop-2-enylcyclohexane Chemical compound C=CCC1CCCCC1 KVOZXXSUSRZIKD-UHFFFAOYSA-N 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 4
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- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 4
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadec-1-ene Chemical compound CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 4
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- 239000000546 pharmaceutical excipient Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- XYXJKPCGSGVSBO-UHFFFAOYSA-N 1,3,5-tris[(4-tert-butyl-3-hydroxy-2,6-dimethylphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C)=C1CN1C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C1=O XYXJKPCGSGVSBO-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000002656 Distearyl thiodipropionate Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 235000019305 distearyl thiodipropionate Nutrition 0.000 description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 3
- 238000007306 functionalization reaction Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 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 3
- 239000003921 oil Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 2
- ZNRLMGFXSPUZNR-UHFFFAOYSA-N 2,2,4-trimethyl-1h-quinoline Chemical compound C1=CC=C2C(C)=CC(C)(C)NC2=C1 ZNRLMGFXSPUZNR-UHFFFAOYSA-N 0.000 description 2
- GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 description 2
- XYFRHHAYSXIKGH-UHFFFAOYSA-N 3-(5-methoxy-2-methoxycarbonyl-1h-indol-3-yl)prop-2-enoic acid Chemical compound C1=C(OC)C=C2C(C=CC(O)=O)=C(C(=O)OC)NC2=C1 XYFRHHAYSXIKGH-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-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
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 239000004971 Cross linker Substances 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 2
- 239000003508 Dilauryl thiodipropionate Substances 0.000 description 2
- SGVYKUFIHHTIFL-UHFFFAOYSA-N Isobutylhexyl Natural products CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 description 2
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
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- 230000000052 comparative effect Effects 0.000 description 2
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- 229940069096 dodecene Drugs 0.000 description 2
- LDLDYFCCDKENPD-UHFFFAOYSA-N ethenylcyclohexane Chemical compound C=CC1CCCCC1 LDLDYFCCDKENPD-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 125000000743 hydrocarbylene group Chemical group 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- VKPSKYDESGTTFR-UHFFFAOYSA-N isododecane Natural products CC(C)(C)CC(C)CC(C)(C)C VKPSKYDESGTTFR-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
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- 125000004430 oxygen atom Chemical group O* 0.000 description 2
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
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- ZOKCNEIWFQCSCM-UHFFFAOYSA-N (2-methyl-4-phenylpent-4-en-2-yl)benzene Chemical compound C=1C=CC=CC=1C(C)(C)CC(=C)C1=CC=CC=C1 ZOKCNEIWFQCSCM-UHFFFAOYSA-N 0.000 description 1
- NWRZGFYWENINNX-UHFFFAOYSA-N 1,1,2-tris(ethenyl)cyclohexane Chemical compound C=CC1CCCCC1(C=C)C=C NWRZGFYWENINNX-UHFFFAOYSA-N 0.000 description 1
- NALFRYPTRXKZPN-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane Chemical compound CC1CC(C)(C)CC(OOC(C)(C)C)(OOC(C)(C)C)C1 NALFRYPTRXKZPN-UHFFFAOYSA-N 0.000 description 1
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
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- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- VTFXHGBOGGGYDO-UHFFFAOYSA-N 2,4-bis(dodecylsulfanylmethyl)-6-methylphenol Chemical compound CCCCCCCCCCCCSCC1=CC(C)=C(O)C(CSCCCCCCCCCCCC)=C1 VTFXHGBOGGGYDO-UHFFFAOYSA-N 0.000 description 1
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 1
- ROHFBIREHKPELA-UHFFFAOYSA-N 2-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]prop-2-enoic acid;methane Chemical compound C.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O ROHFBIREHKPELA-UHFFFAOYSA-N 0.000 description 1
- FDSUVTROAWLVJA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)COCC(CO)(CO)CO FDSUVTROAWLVJA-UHFFFAOYSA-N 0.000 description 1
- JJRDRFZYKKFYMO-UHFFFAOYSA-N 2-methyl-2-(2-methylbutan-2-ylperoxy)butane Chemical compound CCC(C)(C)OOC(C)(C)CC JJRDRFZYKKFYMO-UHFFFAOYSA-N 0.000 description 1
- GAODDBNJCKQQDY-UHFFFAOYSA-N 2-methyl-4,6-bis(octylsulfanylmethyl)phenol Chemical compound CCCCCCCCSCC1=CC(C)=C(O)C(CSCCCCCCCC)=C1 GAODDBNJCKQQDY-UHFFFAOYSA-N 0.000 description 1
- HXIQYSLFEXIOAV-UHFFFAOYSA-N 2-tert-butyl-4-(5-tert-butyl-4-hydroxy-2-methylphenyl)sulfanyl-5-methylphenol Chemical compound CC1=CC(O)=C(C(C)(C)C)C=C1SC1=CC(C(C)(C)C)=C(O)C=C1C HXIQYSLFEXIOAV-UHFFFAOYSA-N 0.000 description 1
- BIISIZOQPWZPPS-UHFFFAOYSA-N 2-tert-butylperoxypropan-2-ylbenzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC=C1 BIISIZOQPWZPPS-UHFFFAOYSA-N 0.000 description 1
- HCILJBJJZALOAL-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)-n'-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyl]propanehydrazide Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)NNC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 HCILJBJJZALOAL-UHFFFAOYSA-N 0.000 description 1
- OGRORDCCINVZKC-UHFFFAOYSA-N 3-[bis(prop-2-enoxy)methoxy]prop-1-ene Chemical compound C=CCOC(OCC=C)OCC=C OGRORDCCINVZKC-UHFFFAOYSA-N 0.000 description 1
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 1
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
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- UQBOJOOOTLPNST-UHFFFAOYSA-N Dehydroalanine Chemical class NC(=C)C(O)=O UQBOJOOOTLPNST-UHFFFAOYSA-N 0.000 description 1
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- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
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- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
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- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- QDHUQRBYCVAWEN-UHFFFAOYSA-N amino prop-2-enoate Chemical class NOC(=O)C=C QDHUQRBYCVAWEN-UHFFFAOYSA-N 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
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Description
本出願は、2014年5月13日に出願された米国仮出願第61/992,338号の利益を主張するものである。
(a)エチレン系ポリマーと、
(b)有機過酸化物と、
(c)少なくとも1種類のアミン含有モノマーを中に組み込んだアミン官能化インターポリマーと、を含む、架橋性ポリマー組成物である。
(a)エチレン系アミン官能化インターポリマーと、
(b)有機過酸化物と、を含む、架橋性ポリマー組成物である。
上述のように、本明細書に記載される架橋性ポリマー組成物の1つの成分は、エチレン系ポリマーである。本明細書で使用されるとき、「エチレン系」ポリマーは、第1級(すなわち、50重量パーセント(「重量%」)を超える)モノマー成分としてエチレンモノマーから調製されるポリマーであるが、他のコモノマーも用いられ得る。「ポリマー」は、同一のまたは異なる種類のモノマーを反応させること(すなわち、重合すること)によって調製される高分子化合物を意味し、ホモポリマー及びインターポリマーを含む。「インターポリマー」は、少なくとも2つの異なる種類のモノマーの重合によって調製されるポリマーを意味する。この一般名称は、コポリマー(通常、2つの異なる種類のモノマーから調製されるポリマーを指すために用いられる)、及び2つを超える異なる種類のモノマーから調製されるポリマー(例えば、ターポリマー(3つの異なる種類のモノマー)及びクオーターポリマー(4つの異なる種類のモノマー))を含む。
架橋性ポリマー組成物の調製は、上記の化合物を配合することを含み得る。例えば、配合は、(1)全ての成分をエチレン系ポリマー中に配合することか、または(2)後述するように浸漬され得る有機過酸化物を除く全ての成分を配合することのいずれかによって行われ得る。架橋性ポリマー組成物の配合は、当業者には既知の標準的な機器によって達成され得る。配合機器の例は、Brabender(商標)、Banbury(商標)、またはBolling(商標)ミキサー等の内部バッチミキサーである。あるいは、Farrel(商標)連続ミキサー、Werner and Pfleiderer(商標)二軸スクリューミキサー、またはBuss(商標)混練連続押出機等の連続一軸または二軸スクリューミキサーが使用され得る。配合は、エチレン系ポリマーの融解温度を超える温度から、エチレン系ポリマーが分解し始める温度までの温度で行われ得る。種々の実施形態において、配合は、100〜200℃または110〜150℃の範囲の温度で行われ得る。
上記の架橋性ポリマー組成物は、架橋エチレン系ポリマーを形成するために、硬化され得るか、または硬化することを可能にされ得る。かかる硬化は、架橋性ポリマー組成物を、175〜260℃の範囲の温度で維持され得る加熱された硬化ゾーン中で高温に供することによって行われ得る。加熱された硬化ゾーンは、加圧蒸気によって加熱され得るか、または加圧窒素ガスによって誘導加熱され得る。その後、架橋ポリマー組成物は、(例えば、周囲温度まで)冷却され得る。
導体及び絶縁層を備えるケーブルは、上記の架橋性ポリマー組成物を用いて調製され得る。「ケーブル」及び「電力ケーブル」は、シース、例えば、絶縁カバー及び/または保護外側ジャケット内の少なくとも1つのワイヤーまたは光ファイバーを意味する。典型的には、ケーブルは、通常、共通の絶縁カバー及び/または保護ジャケット中の共に結合した2つ以上のワイヤーまたは光ファイバーである。シース内部の個々のワイヤーまたはファイバーは、裸であり得るか、カバーされ得るか、または絶縁され得る。組み合わせケーブルは、電線及び光ファイバーの両方を含み得る。典型的なケーブル設計は、米国特許第5,246,783号、同第6,496,629号、及び同第6,714,707号に例示されている。「導体」は、熱、光、及び/または電気を伝導するための1つ以上のワイヤーまたはファイバーを示す。導体は、単一のワイヤー/ファイバーまたは複数のワイヤー/ファイバーであり得、鎖状形態または管状形態であり得る。好適な導体の非限定的な例としては、銀、金、銅、炭素、及びアルミニウム等の金属が挙げられる。導体はまた、ガラスまたはプラスチックのいずれかから作製される光ファイバーであり得る。
ムービングダイレオメータ
Alpha Technologies製のMDR 2000上で、ASTM D5289に記載される方法にそれぞれ従い、182℃でムービングダイレオメータ(「MDR」)試験を行う。硬化可能性を、トルクを記録する間に、182℃に保たれた、溶融した試料上に振動歪みを適用するMDRを使用して決定する。化合物が架橋するにつれ、トルクも増加し、安定した最大トルク、Mhに達する。熱的老化時間(例えば70℃で)の関数としてのMhの比較は、ほぼ周囲条件下の長い保存期間に渡って、硬化可能性を維持する組成物の能力を比較する方法を提供する。
70℃の実験室用オーブン内の、ねじ式キャップの下のMYLAR(商標)フィルムで密封した瓶内で、試料を熱老化させる。適量の材料を、MDR試験のための特定の老化時間の後、瓶から除去し、その後、瓶を再度密封し、さらなる熱老化のためにオーブンに戻す。
十分な量のペレット化された化合物を圧縮成形し、8インチ×8インチ×0.010インチのフレームを満たす。圧縮成形を以下の順番の条件を使用して行う:i)125℃及び125psiで、3分間、ii)125℃及び2500psiで、5分間、iii)焼き入れ−冷却、iv)過剰な水切りを除去し、小片に切断し、さらなるプレス手順を続け、v)125℃及び500psiで、3分間、vi)125℃及び2500psiで、3分間、vii)182℃まで温度を上げ、2500psiで12分間保持し、viii)焼き入れ冷却する。
60−Hzの散逸率を、120℃の温度及び25kV/mmの電気的応力で、試料の架橋したプラークから切断した3インチのディスク上で測定する。これは、Soken製の試料保持器/試験セル、モデルDAC−OBE−7の平らな円形の電極の間に、試料を挿入することによって行われる。温度制御されている油浴を使用して加熱及び循環させる、Solvay Specialty Polymers製のGalden D03ペルフルオロポリエーテルを使用して、試験セルを油で充填する。試料が挿入された1時間後に測定を行い、システムが標的試験温度で熱平衡であることを確実にする。電源を使用して、最大で60Hz、10kVの試験電圧を提供する。Soken製の自動シェーリングブリッジ、モデルDAC−PSC−UAを利用して、Soken製モデルDAC−Cs−102A 1000 pF基準コンデンサで散逸率を測定する。
ASTM D792に従い密度を決定する。
ASTM D1238、条件190℃/2.16kgに従い、メルトインデックス、すなわちI2を測定し、10分当たりに溶出されるグラム数で報告する。
以下の実施例において、下記の材料が用いられる。
以下の方法に従い、対照のエチレンポリマー及び3つのエチレン/アミノアクリレートコポリマーを調製する。
下記の表2に列挙する処方に従い、1つの比較試料(「CS1」)及び3つの試料(「S1−S3」)を調製する。
以下の手順に従い散逸率を決定するために、CS1及びS1〜S3の各々を調製する。実施例2に記載されるように調製した試料の各々を、12ミルのプラーク内にプレスし、上述の通りに架橋する。結果として生じるプラークを、60℃で4日間、真空オーブン内に保存し、架橋反応からの揮発性副生成物を除去する。3−インチのディスクを、プラークから切断し、上記の試験方法に従い散逸率について分析した。結果を下記の表4で提供する。
3つの追加の試料(S4−S6)を、CS1のプレブレンド(過酸化物を含有しない)の一部を使用することによって調製し、S1及びS2のプレブレンドを希釈する。この希釈を、二本ロール機(0.4mmのギャップ、20rpm、約6分間の混合時間、115℃のロール温度、その間、材料を角から切断し、約10回、ロールの中心へ供給する)上で行い、表5の配合物を得る。
下記の表7に列挙する処方に従い、1つの比較試料(「CS2」)及び3つの試料(「S7−S9」)を調製する。
Claims (13)
- (a)エチレン系ポリマーと、
(b)有機過酸化物と、
(c)少なくとも1種類のアミン含有モノマーを中に組み込んだアミン官能化インターポリマーと、
を含む、架橋性ポリマー組成物であって、
前記アミン官能化インターポリマーはエチレンと、2−(ジエチルアミノ)エチルメタクリレート、2−(ジメチルアミノ)エチルメタクリレート、2−(t−ブチルアミノ)エチルメタクリレート及びこれらの混合物から成る群から選択されるアミノアクリレートモノマーの共重合より調製されるエチレン/アミノアクリレートコポリマーであり、
前記アミン含有モノマーは、アミン官能化インターポリマーの調製において用いられるアミン含有モノマー及びオレフィン系モノマーの総合重量に基づいて、0.5〜10重量%の範囲である、
架橋性ポリマー組成物。 - 前記アミン官能化インターポリマーが、前記架橋性ポリマー組成物の1グラム当たり0.1〜200マイクロモルのアミンの範囲のモルアミン含有量をもたらすために十分な量で存在する、請求項1に記載の架橋性ポリマー組成物。
- 少なくとも1つの酸性成分をさらに含む、請求項1に記載の架橋性ポリマー組成物。
- 抗酸化剤をさらに含み、前記抗酸化剤が前記酸性成分の源である、請求項3に記載の架橋性ポリマー組成物。
- 前記エチレン系ポリマーが、前記架橋性ポリマー組成物の全重量に基づいて、50〜99重量パーセントの範囲の量で存在し、前記有機過酸化物が、前記架橋性ポリマー組成物の全重量に基づいて、0.1〜5重量パーセントの範囲の量で存在し、前記アミン官能化インターポリマーが、前記架橋性ポリマー組成物の全重量に基づいて、0.1〜5重量パーセントの範囲の量で存在する、請求項1〜4のいずれか1項に記載の架橋性ポリマー組成物。
- 前記架橋性ポリマー組成物が、前記架橋性ポリマー組成物の調製直後に架橋され、182℃のムービングダイレオメータによる最大トルク(in−lbs)として測定されるとき、初期硬化可能性(CP0)を有し、前記架橋性ポリマー組成物が、70℃で14日間、前記架橋性ポリマー組成物を老化させた後に架橋され、182℃のムービングダイレオメータによる最大トルク(in−lbs)として測定されるとき、熱老化硬化可能性CP14を有し、前記架橋性ポリマー組成物が、少なくとも0.6のCP14とCP0との比を有する、請求項1〜5のいずれか1項に記載の架橋性ポリマー組成物。
- 請求項1〜6のいずれか1項に記載の架橋性ポリマー組成物から調製される、架橋物品。
- 導電性コアと、
前記導電性コアを少なくとも部分的に囲むポリマー層と、を備え、前記ポリマー層の少なくとも一部が、請求項7に記載の架橋物品を含む、被覆導体。 - (a)0.5〜10重量%の少なくとも1種類のアミン含有モノマーを中に組み込んだエチレン系アミン官能化インターポリマーであって、
前記アミン官能化インターポリマーはエチレンと、2−(ジエチルアミノ)エチルメタクリレート、2−(ジメチルアミノ)エチルメタクリレート、2−(t−ブチルアミノ)エチルメタクリレート及びこれらの混合物から成る群から選択されるアミノアクリレートモノマーの共重合より調製されるエチレン/アミノアクリレートコポリマーである、
エチレン系アミン官能化インターポリマー、および
(b)有機過酸化物を含む、
架橋性ポリマー組成物。 - 前記エチレン系アミン官能化インターポリマーが、前記架橋性ポリマー組成物の1グラム当たり0.1〜200マイクロモルのアミンの範囲のモルアミン含有量をもたらすために十分な量で存在する、請求項9に記載の架橋性ポリマー組成物。
- 前記エチレン系アミン官能化インターポリマーが、前記架橋性ポリマー組成物の全重量に基づいて、1〜99重量パーセントの範囲の量で存在し、前記有機過酸化物が、前記架橋性ポリマー組成物の全重量に基づいて、0.1〜5重量パーセントの範囲の量で存在する、請求項9または10に記載の架橋性ポリマー組成物。
- 導電性コアと、
前記導電性コアを少なくとも部分的に囲むポリマー層と、を備え、前記ポリマー層の少なくとも一部が、請求項9〜11のいずれか1項に記載の架橋性ポリマー組成物から調製される架橋ポリマー組成物を含む、被覆導体。 - 前記エチレン系ポリマーが低密度ポリエチレンである、請求項1に記載の架橋ポリマー組成物。
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CA2948260A1 (en) | 2015-11-19 |
EP3143084B1 (en) | 2019-09-18 |
CN106507676A (zh) | 2017-03-15 |
TW201546152A (zh) | 2015-12-16 |
EP3143084A1 (en) | 2017-03-22 |
WO2015175106A1 (en) | 2015-11-19 |
KR20170010312A (ko) | 2017-01-26 |
US10619034B2 (en) | 2020-04-14 |
TWI666255B (zh) | 2019-07-21 |
US20170101528A1 (en) | 2017-04-13 |
KR102366000B1 (ko) | 2022-02-23 |
US11685823B2 (en) | 2023-06-27 |
JP2017516896A (ja) | 2017-06-22 |
CA2948260C (en) | 2022-07-12 |
US20200181375A1 (en) | 2020-06-11 |
CN106507676B (zh) | 2019-12-10 |
MX2016014677A (es) | 2017-07-17 |
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