KR20190066024A - 박리지용 또는 박리 필름용 실리콘 조성물 - Google Patents
박리지용 또는 박리 필름용 실리콘 조성물 Download PDFInfo
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- KR20190066024A KR20190066024A KR1020197011850A KR20197011850A KR20190066024A KR 20190066024 A KR20190066024 A KR 20190066024A KR 1020197011850 A KR1020197011850 A KR 1020197011850A KR 20197011850 A KR20197011850 A KR 20197011850A KR 20190066024 A KR20190066024 A KR 20190066024A
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/40—Adhesives in the form of films or foils characterised by release liners
- C09J7/401—Adhesives in the form of films or foils characterised by release liners characterised by the release coating composition
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- B32B27/00—Layered products comprising a layer of synthetic resin
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/06—Preparatory processes
- C08G77/08—Preparatory processes characterised by the catalysts used
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/017—Antistatic agents
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
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- C—CHEMISTRY; METALLURGY
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- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
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- C08L83/04—Polysiloxanes
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- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/10—Block- or graft-copolymers containing polysiloxane sequences
- C08L83/12—Block- or graft-copolymers containing polysiloxane sequences containing polyether sequences
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- C08G77/04—Polysiloxanes
- C08G77/12—Polysiloxanes containing silicon bound to hydrogen
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- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
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- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/46—Block-or graft-polymers containing polysiloxane sequences containing polyether sequences
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- C09J2453/00—Presence of block copolymer
- C09J2453/005—Presence of block copolymer in the release coating
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- C09J2483/00—Presence of polysiloxane
- C09J2483/005—Presence of polysiloxane in the release coating
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| PCT/JP2017/035208 WO2018066448A1 (ja) | 2016-10-06 | 2017-09-28 | 剥離紙用又は剥離フィルム用シリコーン組成物 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| WO2023182805A1 (ko) * | 2022-03-22 | 2023-09-28 | 주식회사 엘지화학 | 이형 조성물 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA3026619C (en) * | 2016-06-28 | 2024-07-02 | Threebond Co., Ltd. | Composition of hardening resin, fuel cell, and sealing method |
| JP6745153B2 (ja) * | 2016-07-11 | 2020-08-26 | 信越ポリマー株式会社 | 導電性離型層形成用塗料及びその製造方法、並びに導電性離型フィルム及びその製造方法 |
| EP3591008B1 (en) * | 2017-03-02 | 2024-08-21 | Dow Toray Co., Ltd. | Curable silicone composition, cured product of same, and optical display |
| JP2021525294A (ja) * | 2018-05-24 | 2021-09-24 | モメンティブ パフォーマンス マテリアルズ インコーポレイテッドMomentive Performance Materials Inc. | オイルブリード自己結合性液体シリコーンゴム組成物 |
| CN112334561B (zh) * | 2018-06-28 | 2023-08-22 | 信越化学工业株式会社 | 用于剥离纸或剥离膜的有机聚硅氧烷组合物 |
| JP7664677B2 (ja) * | 2018-12-25 | 2025-04-18 | 信越化学工業株式会社 | シリコーン剥離剤組成物、剥離紙及び剥離フィルム |
| KR102891962B1 (ko) * | 2019-01-08 | 2025-12-01 | 신에쓰 가가꾸 고교 가부시끼가이샤 | 박리지 또는 박리 필름용 오가노폴리실록산 조성물 |
| KR20220139369A (ko) * | 2020-02-18 | 2022-10-14 | 신에쓰 가가꾸 고교 가부시끼가이샤 | 박리지 또는 박리 필름 제조용 실리콘 조성물, 및 박리지 또는 박리 필름 |
| KR20220011924A (ko) * | 2020-07-22 | 2022-02-03 | 주식회사 엘지화학 | 실리콘계 코팅 조성물 및 이를 포함하는 실리콘계 이형필름 |
| CN112761022B (zh) * | 2020-12-28 | 2022-09-09 | 广东标美硅氟新材料有限公司 | 一种超轻剥离力有机硅离型剂及其制备方法和应用 |
| JP7626204B2 (ja) * | 2021-04-09 | 2025-02-04 | 信越化学工業株式会社 | 付加反応硬化型オルガノポリシロキサン組成物 |
| JPWO2022250125A1 (enExample) * | 2021-05-28 | 2022-12-01 | ||
| JP7784242B2 (ja) * | 2021-05-28 | 2025-12-11 | 日東電工株式会社 | 積層シートおよび剥離フィルム |
| KR20240052958A (ko) | 2021-08-31 | 2024-04-23 | 다우 실리콘즈 코포레이션 | 정전기 방지 실리콘 이형 코팅 및 이의 제조 및 사용 방법 |
| JP2025505111A (ja) * | 2022-01-28 | 2025-02-21 | ダウ シリコーンズ コーポレーション | シリコーン剥離コーティングエマルジョン、その調製方法、及びベーカリー紙への使用 |
| KR20240144465A (ko) * | 2022-05-30 | 2024-10-02 | 도요보 가부시키가이샤 | 실리콘 이형 폴리에스테르 필름, 및 그 제조 방법 |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2636968B2 (ja) | 1990-02-08 | 1997-08-06 | バイエル・アクチエンゲゼルシヤフト | 新規ポリチオフエンの溶液及びその製造方法 |
| JP2002241613A (ja) | 2001-02-20 | 2002-08-28 | Sony Chem Corp | 帯電防止能を有する剥離剤組成物 |
| WO2005052058A1 (ja) | 2003-11-28 | 2005-06-09 | Idemitsu Kosan Co., Ltd. | 導電性ポリアニリン組成物、その製造方法及びそれからなる成形体 |
| JP2006249303A (ja) | 2005-03-11 | 2006-09-21 | Shin Etsu Polymer Co Ltd | 導電性高分子溶液およびその製造方法 |
| JP2007254730A (ja) | 2006-02-24 | 2007-10-04 | Toyo Ink Mfg Co Ltd | 導電性組成物 |
| JP2008045061A (ja) | 2006-08-18 | 2008-02-28 | Shin Etsu Polymer Co Ltd | 導電性固形物ならびにその製造方法、および導電性高分子溶液 |
| JP2011032382A (ja) | 2009-08-03 | 2011-02-17 | Shin Etsu Polymer Co Ltd | 導電性高分子溶液およびその製造方法 |
| JP2016027128A (ja) | 2014-06-26 | 2016-02-18 | 三洋化成工業株式会社 | シリコーン粘着剤用帯電防止剤及び帯電防止性シリコーン粘着剤 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05320625A (ja) * | 1992-05-18 | 1993-12-03 | Marubishi Yuka Kogyo Kk | 帯電防止剤組成物 |
| JP2012157978A (ja) * | 2011-01-28 | 2012-08-23 | Dow Corning Toray Co Ltd | 積層体及びその帯電防止乃至低減方法 |
| JP5794207B2 (ja) * | 2012-06-07 | 2015-10-14 | 信越化学工業株式会社 | 付加硬化型シリコーンエマルジョン組成物及び剥離フィルム |
| JP5852995B2 (ja) * | 2013-07-18 | 2016-02-09 | 藤森工業株式会社 | 帯電防止表面保護フィルムの製造方法、及び帯電防止表面保護フィルム |
| JP6331956B2 (ja) * | 2014-10-17 | 2018-05-30 | 信越化学工業株式会社 | 剥離シート用オルガノポリシロキサン組成物及び剥離シート |
| JP6232454B2 (ja) * | 2015-02-06 | 2017-11-15 | 三洋化成工業株式会社 | シリコーン剥離剤用帯電防止剤及び帯電防止性シリコーン剥離フィルム |
| CN107960100B (zh) * | 2015-04-28 | 2021-04-02 | 信越化学工业株式会社 | 有机硅粘合剂组合物和胶带 |
-
2016
- 2016-10-06 JP JP2016198226A patent/JP2018059001A/ja active Pending
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2017
- 2017-09-28 KR KR1020197011850A patent/KR20190066024A/ko not_active Ceased
- 2017-09-28 US US16/339,897 patent/US20200048508A1/en not_active Abandoned
- 2017-09-28 WO PCT/JP2017/035208 patent/WO2018066448A1/ja not_active Ceased
- 2017-09-28 EP EP17858286.2A patent/EP3524655A4/en not_active Withdrawn
- 2017-09-28 CN CN201780061784.0A patent/CN109863219A/zh active Pending
- 2017-10-05 TW TW106134292A patent/TW201829622A/zh unknown
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2636968B2 (ja) | 1990-02-08 | 1997-08-06 | バイエル・アクチエンゲゼルシヤフト | 新規ポリチオフエンの溶液及びその製造方法 |
| JP2002241613A (ja) | 2001-02-20 | 2002-08-28 | Sony Chem Corp | 帯電防止能を有する剥離剤組成物 |
| WO2005052058A1 (ja) | 2003-11-28 | 2005-06-09 | Idemitsu Kosan Co., Ltd. | 導電性ポリアニリン組成物、その製造方法及びそれからなる成形体 |
| JP2006249303A (ja) | 2005-03-11 | 2006-09-21 | Shin Etsu Polymer Co Ltd | 導電性高分子溶液およびその製造方法 |
| JP2007254730A (ja) | 2006-02-24 | 2007-10-04 | Toyo Ink Mfg Co Ltd | 導電性組成物 |
| JP2008045061A (ja) | 2006-08-18 | 2008-02-28 | Shin Etsu Polymer Co Ltd | 導電性固形物ならびにその製造方法、および導電性高分子溶液 |
| JP2011032382A (ja) | 2009-08-03 | 2011-02-17 | Shin Etsu Polymer Co Ltd | 導電性高分子溶液およびその製造方法 |
| JP2016027128A (ja) | 2014-06-26 | 2016-02-18 | 三洋化成工業株式会社 | シリコーン粘着剤用帯電防止剤及び帯電防止性シリコーン粘着剤 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2023182805A1 (ko) * | 2022-03-22 | 2023-09-28 | 주식회사 엘지화학 | 이형 조성물 |
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|---|---|
| WO2018066448A1 (ja) | 2018-04-12 |
| EP3524655A1 (en) | 2019-08-14 |
| US20200048508A1 (en) | 2020-02-13 |
| CN109863219A (zh) | 2019-06-07 |
| JP2018059001A (ja) | 2018-04-12 |
| EP3524655A4 (en) | 2020-06-03 |
| TW201829622A (zh) | 2018-08-16 |
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