CN104169335B - 离子有机硅的可固化组合物 - Google Patents
离子有机硅的可固化组合物 Download PDFInfo
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- CN104169335B CN104169335B CN201280070542.5A CN201280070542A CN104169335B CN 104169335 B CN104169335 B CN 104169335B CN 201280070542 A CN201280070542 A CN 201280070542A CN 104169335 B CN104169335 B CN 104169335B
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Classifications
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- 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
- C08G77/80—Siloxanes having aromatic substituents, e.g. phenyl side groups
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
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- A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
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- A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
- A61K8/899—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing sulfur, e.g. sodium PG-propyldimethicone thiosulfate copolyol
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- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
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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
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
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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
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- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/392—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing sulfur
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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
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/395—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing phosphorus
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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
- 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
- C08L83/04—Polysiloxanes
- C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
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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
- 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
- C08L83/04—Polysiloxanes
- C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
-
- 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
- C09J183/00—Adhesives based on 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; Adhesives based on derivatives of such polymers
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- C09J183/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen, and oxygen
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/10—General cosmetic use
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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
- C08G77/12—Polysiloxanes containing silicon bound to hydrogen
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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
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
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- Birds (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Dermatology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silicon Polymers (AREA)
- Adhesives Or Adhesive Processes (AREA)
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| PCT/US2012/070953 WO2013103535A1 (en) | 2012-01-04 | 2012-12-20 | Curable compositions of ionic silicones |
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Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US8772422B2 (en) * | 2012-01-04 | 2014-07-08 | Momentive Performance Materials Inc. | Polymer composites of silicone ionomers |
| JP6165775B2 (ja) * | 2012-01-04 | 2017-07-26 | 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 | イオン性シリコーンを含むフリーラジカル重合性組成物 |
| US9746391B2 (en) | 2013-10-30 | 2017-08-29 | Alphinity, Llc | Fluid monitoring device with disposable inner liner with sensor integration |
| EP3094960B1 (en) | 2014-01-17 | 2019-07-31 | Alphinity, LLC | Fluid monitoring assembly with sensor functionality |
| CN103865475B (zh) * | 2014-03-26 | 2016-02-17 | 苏州桐力光电技术服务有限公司 | 一种透明有机硅凝胶粘接剂 |
| BR112016025241B8 (pt) | 2014-04-28 | 2022-03-29 | Dow Corning | Composição reticulada, composição cosmética, e, método de formar uma composição reticulada |
| US10597496B2 (en) | 2014-09-19 | 2020-03-24 | Momentive Performance Materials Inc. | Platinum (II) diene complexes for controlled siloxane crosslinking |
| US9839602B2 (en) * | 2014-12-16 | 2017-12-12 | Momentive Performance Materials Inc. | Personal care compositions containing crosslinked silicone polymer networks and their method of preparation |
| US9498409B2 (en) | 2014-12-16 | 2016-11-22 | Momentive Performance Materials Inc. | Cosmetic skin covering sheets and their method of preparation |
| US9801805B2 (en) | 2014-12-16 | 2017-10-31 | Momentive Performance Materials Inc. | Personal care composition comprising silicone network |
| US20160166494A1 (en) * | 2014-12-16 | 2016-06-16 | Momentive Performance Materials Inc. | Cosmetic composition and method of preparation |
| US9744119B2 (en) | 2014-12-16 | 2017-08-29 | Momentive Performance Materials Inc. | Cosmetic composition and method of preparation |
| EP3234424B1 (en) | 2014-12-19 | 2022-03-16 | Repligen Corporation | Encapsulated system for pressurized fluid processes |
| CN107428943A (zh) * | 2015-03-06 | 2017-12-01 | 皇家飞利浦有限公司 | 口腔护理物质的递送 |
| CN104725864A (zh) * | 2015-04-08 | 2015-06-24 | 杭州歌方新材料科技有限公司 | 一种抗菌硅橡胶及其制备方法 |
| WO2016175129A1 (ja) * | 2015-04-28 | 2016-11-03 | 信越化学工業株式会社 | シリコーン粘着剤組成物および粘着テープ |
| CN105086929B (zh) * | 2015-08-10 | 2017-07-18 | 东莞市新星有机硅科技有限公司 | 耐冲击有机硅封装胶的制备方法 |
| KR102117416B1 (ko) * | 2016-09-26 | 2020-06-01 | 닛토덴코 가부시키가이샤 | 점착제 조성물, 점착 시트, 및 광학 부재 |
| EP3555213B1 (en) * | 2016-12-19 | 2022-01-26 | Saint-Gobain Performance Plastics Corporation | Silicone-based composition and article made therefrom |
| CN106519947A (zh) * | 2016-12-30 | 2017-03-22 | 苏州科立盈胶粘材料有限公司 | 基于石墨烯材料的透明抗静电涂层、抗静电功能膜及抗静电功能膜的制备方法 |
| JP6733562B2 (ja) * | 2017-01-20 | 2020-08-05 | 信越化学工業株式会社 | 水性シリコーン分散液、皮膜及び化粧料 |
| JP6395173B1 (ja) * | 2017-03-29 | 2018-09-26 | 三菱電機株式会社 | パワー半導体モジュール |
| WO2018179573A1 (ja) * | 2017-03-29 | 2018-10-04 | 三菱電機株式会社 | パワー半導体モジュール |
| US10314381B1 (en) * | 2017-07-01 | 2019-06-11 | Hanover Premium LLC | Haircutting collar, method of making and using |
| US10344194B2 (en) * | 2017-09-27 | 2019-07-09 | Momentive Performance Materials Inc. | Thermal interface composition comprising ionically modified siloxane |
| CN108079949B (zh) * | 2017-12-27 | 2020-11-13 | 湖南大学 | 利用磁性猪粪生物炭去除水体中铅的方法 |
| CN108144581B (zh) * | 2017-12-27 | 2020-11-13 | 湖南大学 | 碱改性猪粪生物炭及其制备方法和应用 |
| CN108852902B (zh) * | 2018-08-24 | 2021-02-09 | 福州峰禧知识产权服务有限公司 | 一种石墨烯染发剂的制备方法及石墨烯染发剂 |
| EP3886927B1 (en) * | 2018-11-29 | 2023-06-14 | Ethicon, Inc | Low temperature cured silicone lubricious coatings |
| US10632066B1 (en) | 2019-02-01 | 2020-04-28 | The Population Council, Inc. | Method of providing birth control |
| US10918649B2 (en) * | 2019-06-21 | 2021-02-16 | The Population Council, Inc. | System for providing birth control |
| US11529308B2 (en) | 2019-06-21 | 2022-12-20 | The Population Council, Inc. | System for providing birth control |
| CN110694118A (zh) * | 2019-09-23 | 2020-01-17 | 江苏理工学院 | 一种抗菌抗凝血脑室腹腔分流管硅胶管体及其制备方法和应用 |
| CN111019356B (zh) * | 2019-12-20 | 2021-11-23 | 佛山国防科技工业技术成果产业化应用推广中心 | 压力敏感型多孔导电橡胶及其制备方法 |
| GB2592398A (en) * | 2020-02-27 | 2021-09-01 | Copper Clothing Ltd | Antimicrobial material |
| EP3915416A4 (en) * | 2020-03-17 | 2022-11-02 | Wavecompany Co., Ltd. | ADHESIVE SILICONE PATTERN MATERIAL AND CLOTHING WITH IT |
| US11718753B2 (en) | 2020-05-28 | 2023-08-08 | Ethicon, Inc. | Topical skin closure compositions and systems |
| US11518604B2 (en) | 2020-05-28 | 2022-12-06 | Ethicon, Inc. | Systems, methods and devices for aerosol spraying of silicone based topical skin adhesives for sealing wounds |
| US11712229B2 (en) | 2020-05-28 | 2023-08-01 | Ethicon, Inc. | Systems, devices and methods for dispensing and curing silicone based topical skin adhesives |
| US12465577B2 (en) | 2020-05-28 | 2025-11-11 | Ethicon, Inc. | Antimicrobial topical skin closure compositions and systems |
| US11479669B2 (en) | 2020-05-28 | 2022-10-25 | Ethicon, Inc. | Topical skin closure compositions and systems |
| US11589867B2 (en) | 2020-05-28 | 2023-02-28 | Ethicon, Inc. | Anisotropic wound closure systems |
| GB202008978D0 (en) * | 2020-06-12 | 2020-07-29 | Amicoat As | Antimicrobial formulation |
| EP4189155A1 (fr) * | 2020-07-30 | 2023-06-07 | Elkem Silicones France SAS | Procede d'enduction d'un support textile |
| WO2022129348A1 (fr) * | 2020-12-16 | 2022-06-23 | Elkem Silicones France Sas | Composition silicone biocide applicable sur des surfaces |
| US20250051547A1 (en) * | 2022-01-28 | 2025-02-13 | Nano And Advanced Materials Institute Limited | Antimicrobial compositions with enhanced efficacy and prolonged performance lifetime, and preparation method thereof |
| GB2639863A (en) * | 2024-03-25 | 2025-10-08 | Adv Med Solutions Ltd | Silicone polymers comprising active agents |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5532399A (en) * | 1991-10-24 | 1996-07-02 | Wacker-Chemie Gmbh | Process for the preparation or organosilicon compounds carrying sulfur-containing organic radicals |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2968643A (en) | 1958-12-31 | 1961-01-17 | Union Carbide Corp | Sulfo-aralkylsiloxanes and salts thereof |
| US4495340A (en) * | 1983-12-23 | 1985-01-22 | Dow Corning Corporation | Curable masses producing carboxyfunctional silicone coatings |
| US4523002A (en) | 1984-01-04 | 1985-06-11 | General Electric Company | Ionically cross-linked siloxane polymers |
| US4525567A (en) | 1984-01-04 | 1985-06-25 | General Electric Company | Ionically cross-linked siloxane polymers |
| JPH0655898B2 (ja) * | 1989-08-01 | 1994-07-27 | 信越化学工業株式会社 | 硬化性オルガノポリシロキサン組成物 |
| EP0581296A2 (en) | 1992-07-30 | 1994-02-02 | Dow Corning Toray Silicone Co., Ltd. | Ionically conductive organosiloxane polymer compositions |
| JPH06247827A (ja) | 1993-02-22 | 1994-09-06 | Pola Chem Ind Inc | メイクアップ化粧料 |
| JPH06247835A (ja) | 1993-02-22 | 1994-09-06 | Pola Chem Ind Inc | 基礎化粧料 |
| FR2820746A1 (fr) * | 2001-02-09 | 2002-08-16 | Essilor Int | Materiau polymere hydrophile comprenant une matrice reticulee de polyorganosiloxanes et son procede de fabrication |
| WO2005102403A1 (en) * | 2004-04-08 | 2005-11-03 | Dow Corning Corporation | Silicone skin adhesive gels |
| DE602005011330D1 (de) | 2004-12-15 | 2009-01-08 | Dow Corning | Sulfonatfunktionelle organopolysiloxane |
| DE102005057460A1 (de) * | 2005-12-01 | 2007-06-06 | Wacker Chemie Ag | Zu hochfesten Elastomeren vernetzbare ionisch und/oder organometallisch funktionalisierte Siliconpolymere |
| IES20060794A2 (en) | 2006-10-27 | 2008-06-11 | Gerard Francis Hamilton | Lighting apparatus |
| JP5416715B2 (ja) * | 2007-12-21 | 2014-02-12 | ダウ・コーニング・コーポレイション | イオノマー性シリコーン熱可塑性エラストマー |
| DE102008000156A1 (de) * | 2008-01-25 | 2009-07-30 | Wacker Chemie Ag | Durch Bestrahlung aktivierte Hydrosilylierungsreaktionen |
| US8772422B2 (en) * | 2012-01-04 | 2014-07-08 | Momentive Performance Materials Inc. | Polymer composites of silicone ionomers |
| JP6165775B2 (ja) * | 2012-01-04 | 2017-07-26 | 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 | イオン性シリコーンを含むフリーラジカル重合性組成物 |
| US8974775B2 (en) * | 2012-01-04 | 2015-03-10 | Momentive Performance Materials Inc. | Silicone ionomer composition |
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Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US5532399A (en) * | 1991-10-24 | 1996-07-02 | Wacker-Chemie Gmbh | Process for the preparation or organosilicon compounds carrying sulfur-containing organic radicals |
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| KR20140116902A (ko) | 2014-10-06 |
| KR102073565B1 (ko) | 2020-02-05 |
| US8703881B2 (en) | 2014-04-22 |
| US20130171265A1 (en) | 2013-07-04 |
| EP2800775B1 (en) | 2018-04-18 |
| JP6231014B2 (ja) | 2017-11-15 |
| JP2015511969A (ja) | 2015-04-23 |
| EP2800775A1 (en) | 2014-11-12 |
| WO2013103535A1 (en) | 2013-07-11 |
| CN104169335A (zh) | 2014-11-26 |
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