CN104903102B - 叠层膜 - Google Patents
叠层膜 Download PDFInfo
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- CN104903102B CN104903102B CN201380069404.XA CN201380069404A CN104903102B CN 104903102 B CN104903102 B CN 104903102B CN 201380069404 A CN201380069404 A CN 201380069404A CN 104903102 B CN104903102 B CN 104903102B
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- 239000012528 membrane Substances 0.000 title abstract 2
- 239000005642 Oleic acid Substances 0.000 claims abstract description 51
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims abstract description 51
- 238000006073 displacement reaction Methods 0.000 claims abstract description 41
- -1 dimethyl siloxane3)+The fragment ions Chemical class 0.000 claims description 205
- 239000002344 surface layer Substances 0.000 claims description 176
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- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 87
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- 239000011347 resin Substances 0.000 claims description 77
- 150000002500 ions Chemical class 0.000 claims description 71
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 47
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 47
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 47
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 47
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 47
- 238000000034 method Methods 0.000 claims description 46
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims description 45
- 239000012634 fragment Substances 0.000 claims description 41
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 31
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- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 11
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 10
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 9
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- 238000013532 laser treatment Methods 0.000 description 1
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- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- DCBBWYIVFRLKCD-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-2-methylprop-2-enamide Chemical compound CN(C)CCNC(=O)C(C)=C DCBBWYIVFRLKCD-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
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- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- 229940065472 octyl acrylate Drugs 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000011146 organic particle Substances 0.000 description 1
- SWRXNKAASPLSKC-UHFFFAOYSA-N oxalic acid N-phenylaniline Chemical compound C1(=CC=CC=C1)NC1=CC=CC=C1.C(C(=O)O)(=O)O SWRXNKAASPLSKC-UHFFFAOYSA-N 0.000 description 1
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- 125000005429 oxyalkyl group Chemical group 0.000 description 1
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- 125000002081 peroxide 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
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
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- 230000000379 polymerizing effect Effects 0.000 description 1
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- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
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- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
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- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
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- PCADGSDEFOMDNL-UHFFFAOYSA-N tri(propan-2-yloxy)-(3,3,3-trifluoropropyl)silane Chemical compound CC(C)O[Si](OC(C)C)(OC(C)C)CCC(F)(F)F PCADGSDEFOMDNL-UHFFFAOYSA-N 0.000 description 1
- WEUBQNJHVBMUMD-UHFFFAOYSA-N trichloro(3,3,3-trifluoropropyl)silane Chemical compound FC(F)(F)CC[Si](Cl)(Cl)Cl WEUBQNJHVBMUMD-UHFFFAOYSA-N 0.000 description 1
- 229940087291 tridecyl alcohol Drugs 0.000 description 1
- ZLGWXNBXAXOQBG-UHFFFAOYSA-N triethoxy(3,3,3-trifluoropropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCC(F)(F)F ZLGWXNBXAXOQBG-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 238000004846 x-ray emission Methods 0.000 description 1
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/40—Layered products comprising a layer of synthetic resin comprising polyurethanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
- B32B27/283—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polysiloxanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
- B32B27/285—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polyethers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/75—Printability
Landscapes
- Laminated Bodies (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (5)
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JP2013001516 | 2013-01-09 | ||
JP2013-001516 | 2013-01-09 | ||
JP2013-179071 | 2013-08-30 | ||
JP2013179071 | 2013-08-30 | ||
PCT/JP2013/083550 WO2014109177A1 (ja) | 2013-01-09 | 2013-12-16 | 積層フィルム |
Publications (2)
Publication Number | Publication Date |
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CN104903102A CN104903102A (zh) | 2015-09-09 |
CN104903102B true CN104903102B (zh) | 2017-12-19 |
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CN201380069404.XA Active CN104903102B (zh) | 2013-01-09 | 2013-12-16 | 叠层膜 |
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JP (1) | JP6375946B2 (ja) |
KR (1) | KR102281542B1 (ja) |
CN (1) | CN104903102B (ja) |
TW (1) | TWI609784B (ja) |
WO (1) | WO2014109177A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107141226A (zh) * | 2017-06-15 | 2017-09-08 | 温州大学 | 基于1,3‑二[三(羟甲基)甲氨基]丙烷合成六臂引发剂或八臂引发剂的方法 |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6325324B2 (ja) * | 2014-04-15 | 2018-05-16 | リンテック株式会社 | ハードコートフィルム、ハードコート層形成用塗工液およびハードコートフィルムの製造方法 |
JP7143054B2 (ja) * | 2016-03-31 | 2022-09-28 | 大日本印刷株式会社 | 化粧シート及びこれを用いた成型品 |
JP7098268B2 (ja) * | 2016-03-31 | 2022-07-11 | 大日本印刷株式会社 | 化粧シート及びこれを用いた成型品 |
JP6805692B2 (ja) * | 2016-03-31 | 2020-12-23 | 大日本印刷株式会社 | 化粧シート及びこれを用いた成型品 |
KR102291307B1 (ko) * | 2016-09-16 | 2021-08-20 | 다이니폰 인사츠 가부시키가이샤 | 화장 시트 및 화장판 |
CN107043593A (zh) * | 2016-12-30 | 2017-08-15 | 佛山佛塑科技集团股份有限公司 | 一种防油污自修复的塑料薄膜及其涂料 |
CN106800878A (zh) * | 2016-12-30 | 2017-06-06 | 佛山佛塑科技集团股份有限公司 | 一种防油污自修复的塑料薄膜及其涂料 |
JPWO2018128073A1 (ja) * | 2017-01-06 | 2019-11-07 | コニカミノルタ株式会社 | 自己修復膜、自己修復フィルム及び自己修復膜の製造方法 |
KR102118200B1 (ko) | 2017-05-18 | 2020-06-03 | 한양대학교 산학협력단 | 물리적 가교제를 함유하는 자가복원 고분자 네트워크, 이를 위한 조성물, 및 이를 포함하는 광학소자 |
WO2018212511A1 (ko) * | 2017-05-18 | 2018-11-22 | 한양대학교 산학협력단 | 물리적 가교제를 함유하는 자가복원 고분자 네트워크, 이를 위한 조성물, 및 이를 포함하는 광학소자 |
CN111902509B (zh) * | 2018-03-29 | 2022-05-31 | 琳得科株式会社 | 接合用层叠体、接合2个被粘物的方法、以及接合结构体的制造方法 |
KR102164772B1 (ko) * | 2018-04-10 | 2020-10-14 | 주식회사 엘지화학 | 장식 부재 |
US11001719B2 (en) | 2018-09-14 | 2021-05-11 | Rohr, Inc. | Multi-layer coating for a flow surface of an aircraft component |
US20210388490A1 (en) * | 2018-10-23 | 2021-12-16 | Sumitomo Chemical Company, Limited | Laminated body, flexible electronic device, and laminated-body manufacturing method |
CN111892515A (zh) * | 2019-12-29 | 2020-11-06 | 山东远联化工股份有限公司 | 一种脲基螯合剂的生产方法及生产装置 |
JP2023052716A (ja) * | 2020-03-16 | 2023-04-12 | Agc株式会社 | 塗料及び塗膜付き基材 |
JP7495838B2 (ja) * | 2020-07-29 | 2024-06-05 | キヤノン株式会社 | シミュレーション方法、シミュレーション装置、膜形成装置、物品の製造方法及びプログラム |
CN114805422B (zh) * | 2022-05-17 | 2024-08-27 | 山东博苑医药化学股份有限公司 | 一种烷胺釜残回收硅醚的方法 |
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Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3926461B2 (ja) | 1998-02-13 | 2007-06-06 | ナトコ株式会社 | 塗料組成物 |
JP4099769B2 (ja) * | 2003-11-19 | 2008-06-11 | 荒川化学工業株式会社 | メトキシシリル基含有シラン変性ポリイミドシロキサン樹脂の製造法、当該樹脂、当該樹脂組成物、硬化膜および金属箔積層体 |
CN101300294B (zh) * | 2005-09-12 | 2011-09-07 | 东丽株式会社 | 层合薄膜 |
JP2009098654A (ja) * | 2007-09-28 | 2009-05-07 | Dainippon Printing Co Ltd | 光学積層体、偏光板及び画像表示装置 |
JP2009122416A (ja) | 2007-11-15 | 2009-06-04 | Toppan Printing Co Ltd | 光学薄膜フィルム |
CN102421580B (zh) * | 2009-05-12 | 2016-04-20 | 大金工业株式会社 | 转印片及其制造方法 |
JP5476843B2 (ja) * | 2009-08-04 | 2014-04-23 | 大日本印刷株式会社 | 光学積層体、偏光板及び画像表示装置 |
JP2011099744A (ja) | 2009-11-05 | 2011-05-19 | Nippon Paint Co Ltd | 耐指紋性評価方法および耐指紋性被膜 |
US8980432B2 (en) * | 2010-04-27 | 2015-03-17 | Toray Industries, Inc. | Multilayer film and molded body |
EP2711182B1 (en) * | 2011-05-16 | 2021-06-23 | Toray Industries, Inc. | Laminated film and molded body |
WO2013008645A1 (ja) * | 2011-07-11 | 2013-01-17 | 東レ株式会社 | 成形材料、塗料組成物および成形材料の製造方法 |
JP6102735B2 (ja) * | 2012-01-13 | 2017-03-29 | 東レ株式会社 | 成形材料、塗料組成物および成形材料の製造方法 |
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2013
- 2013-12-16 WO PCT/JP2013/083550 patent/WO2014109177A1/ja active Application Filing
- 2013-12-16 CN CN201380069404.XA patent/CN104903102B/zh active Active
- 2013-12-16 JP JP2014509546A patent/JP6375946B2/ja active Active
- 2013-12-16 KR KR1020157017110A patent/KR102281542B1/ko active IP Right Grant
- 2013-12-20 TW TW102147446A patent/TWI609784B/zh active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN107141226A (zh) * | 2017-06-15 | 2017-09-08 | 温州大学 | 基于1,3‑二[三(羟甲基)甲氨基]丙烷合成六臂引发剂或八臂引发剂的方法 |
Also Published As
Publication number | Publication date |
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JP6375946B2 (ja) | 2018-08-22 |
JPWO2014109177A1 (ja) | 2017-01-19 |
TW201429721A (zh) | 2014-08-01 |
KR20150113950A (ko) | 2015-10-08 |
TWI609784B (zh) | 2018-01-01 |
WO2014109177A1 (ja) | 2014-07-17 |
CN104903102A (zh) | 2015-09-09 |
KR102281542B1 (ko) | 2021-07-26 |
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