BR112014013594B1 - composição adesiva estrutural e substrato revestido - Google Patents
composição adesiva estrutural e substrato revestido Download PDFInfo
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- BR112014013594B1 BR112014013594B1 BR112014013594-0A BR112014013594A BR112014013594B1 BR 112014013594 B1 BR112014013594 B1 BR 112014013594B1 BR 112014013594 A BR112014013594 A BR 112014013594A BR 112014013594 B1 BR112014013594 B1 BR 112014013594B1
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- Prior art keywords
- epoxy
- adduct
- anhydride
- fact
- diacid
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 112
- 239000000758 substrate Substances 0.000 title claims abstract description 12
- 239000000853 adhesive Substances 0.000 title claims description 100
- 230000001070 adhesive effect Effects 0.000 title claims description 100
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- 150000001875 compounds Chemical class 0.000 claims abstract description 76
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 72
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- 150000008064 anhydrides Chemical class 0.000 claims abstract description 37
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- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 42
- 239000000463 material Substances 0.000 description 37
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 21
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- 230000015572 biosynthetic process Effects 0.000 description 17
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- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 9
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- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 7
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- PMMYEEVYMWASQN-DMTCNVIQSA-N Hydroxyproline Chemical compound O[C@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-DMTCNVIQSA-N 0.000 description 5
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 5
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- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/182—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing using pre-adducts of epoxy compounds with curing agents
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
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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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4246—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof polymers with carboxylic terminal groups
- C08G59/4269—Macromolecular compounds obtained by reactions other than those involving unsaturated carbon-to-carbon bindings
- C08G59/4276—Polyesters
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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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
- C08G59/5006—Amines aliphatic
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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
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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
- C09J1/00—Adhesives based on inorganic constituents
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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
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
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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
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- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
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- Adhesives Or Adhesive Processes (AREA)
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| PCT/US2012/068378 WO2013086277A2 (en) | 2011-12-09 | 2012-12-07 | Structural adhesive compositions |
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| US20120128499A1 (en) * | 2010-11-19 | 2012-05-24 | Desai Umesh C | Structural adhesive compositions |
| US8796361B2 (en) | 2010-11-19 | 2014-08-05 | Ppg Industries Ohio, Inc. | Adhesive compositions containing graphenic carbon particles |
| US20140150970A1 (en) * | 2010-11-19 | 2014-06-05 | Ppg Industries Ohio, Inc. | Structural adhesive compositions |
| US10294375B2 (en) * | 2011-09-30 | 2019-05-21 | Ppg Industries Ohio, Inc. | Electrically conductive coatings containing graphenic carbon particles |
| US12421118B2 (en) | 2011-09-30 | 2025-09-23 | Ppg Industries Ohio, Inc. | Graphenic carbon particles |
| KR102111816B1 (ko) * | 2012-08-03 | 2020-05-15 | 오씨브이 인텔렉츄얼 캐피탈 엘엘씨 | 개선된 파이버글라스 보강 복합재 |
| CA2903945C (en) * | 2013-03-04 | 2018-05-01 | Nippon Steel & Sumitomo Metal Corporation | Impact-absorbing component |
| SG11201510248YA (en) * | 2013-06-14 | 2016-01-28 | Ppg Ind Ohio Inc | Structural adhesive compositions |
| KR20160034330A (ko) * | 2013-07-24 | 2016-03-29 | 블루 큐브 아이피 엘엘씨 | 경화성 조성물 |
| CN104004482A (zh) * | 2014-06-13 | 2014-08-27 | 江苏悦达新材料科技有限公司 | 一种环氧/有机硅/石墨烯杂化高导热胶粘剂及其制备方法 |
| GB201411586D0 (en) * | 2014-06-30 | 2014-08-13 | Hexcel Composites Ltd | Adhesive composition |
| DE102014226826A1 (de) | 2014-12-22 | 2016-06-23 | Henkel Ag & Co. Kgaa | Epoxidharz-Zusammensetzung |
| US11242427B2 (en) | 2015-10-20 | 2022-02-08 | Ppg Industries Ohio, Inc. | Structural adhesive compositions |
| US10377928B2 (en) | 2015-12-10 | 2019-08-13 | Ppg Industries Ohio, Inc. | Structural adhesive compositions |
| US10351661B2 (en) | 2015-12-10 | 2019-07-16 | Ppg Industries Ohio, Inc. | Method for producing an aminimide |
| CN106118571A (zh) * | 2016-06-28 | 2016-11-16 | 四川东树新材料有限公司 | 风电叶片用含石墨烯结构胶黏剂及其制备方法 |
| CN110072915A (zh) * | 2016-10-28 | 2019-07-30 | 陶氏环球技术有限责任公司 | 具有改善的低温耐冲击性的耐碰撞环氧粘合剂 |
| US11739241B2 (en) | 2017-06-23 | 2023-08-29 | Ddp Specialty Electronic Material Us, Llc | High temperature epoxy adhesive formulations |
| TWI761598B (zh) | 2017-09-20 | 2022-04-21 | 美商片片堅俄亥俄州工業公司 | 雙成份結構之黏著劑及其使用方法 |
| US11732125B2 (en) | 2018-02-09 | 2023-08-22 | Ppg Industries Ohio, Inc. | Coating compositions |
| MX2021003324A (es) | 2018-09-20 | 2021-05-14 | Ppg Ind Ohio Inc | Composicion que contiene tiol. |
| WO2020077333A1 (en) | 2018-10-12 | 2020-04-16 | Ppg Industries Ohio, Inc. | Compositions containing thermally conductive fillers |
| CN112969738B (zh) * | 2018-10-29 | 2025-03-28 | 泽菲罗斯有限公司 | 改进的结构粘结粘合剂 |
| FR3098817A1 (fr) | 2019-07-16 | 2021-01-22 | Ppg Industries Ohio, Inc. | Compositions contenant des charges thermiquement conductrices |
| CN114585701B (zh) * | 2019-08-23 | 2024-04-09 | Ppg工业俄亥俄公司 | 用于改进双组分结构粘合剂的搭接剪切强度和位移的体系和方法 |
| BR112022003302A2 (pt) | 2019-08-23 | 2022-06-21 | Ppg Ind Ohio Inc | Composições de revestimento |
| EP4017897A1 (en) * | 2019-08-23 | 2022-06-29 | PRC-Desoto International, Inc. | Coating compositions |
| EP4017898B1 (en) * | 2019-08-23 | 2026-04-29 | PPG Industries Ohio Inc. | Systems and methods for improved lap shear strength and displacement of two-component structural adhesives |
| US20220372207A1 (en) | 2019-09-23 | 2022-11-24 | Ppg Industries Ohio, Inc. | Curable compositions |
| CN114829476B (zh) | 2019-12-11 | 2024-04-12 | Ppg工业俄亥俄公司 | 含有导热填料的组合物 |
| EP4110871A1 (en) | 2020-02-26 | 2023-01-04 | PPG Industries Ohio Inc. | Coated substrates and methods of preparing the same |
| US20230115050A1 (en) | 2020-02-26 | 2023-04-13 | Ppg Industries Ohio, Inc. | Thermally conductive and electrically insulating powder coating compositions |
| KR20220143746A (ko) | 2020-02-26 | 2022-10-25 | 피피지 인더스트리즈 오하이오 인코포레이티드 | 2-층 유전체 코팅 |
| CN115702189A (zh) | 2020-04-15 | 2023-02-14 | Ppg工业俄亥俄公司 | 含有导热填料的组合物 |
| ES3040286T3 (en) | 2020-04-15 | 2025-10-29 | Ppg Ind Ohio Inc | Use of a coating formed from a composition containing thermally conductive fillers to provide a substrate with thermal and fire protection |
| CA3175421A1 (en) | 2020-04-15 | 2021-10-21 | Liang Ma | Compositions containing thermally conductive fillers |
| EP4136162A1 (en) | 2020-04-15 | 2023-02-22 | PPG Industries Ohio Inc. | Compositions containing thermally conductive fillers |
| WO2021211182A1 (en) | 2020-04-15 | 2021-10-21 | Ppg Industries Ohio, Inc. | Compositions containing thermally conductive fillers |
| WO2021211185A1 (en) | 2020-04-15 | 2021-10-21 | Ppg Industries Ohio, Inc. | Compositions containing thermally conductive fillers |
| CA3199506A1 (en) | 2020-12-18 | 2022-06-23 | Corey James DEDOMENIC | Thermally conductive and electrically insulating and/or fire-retardant electrodepositable coating compositions |
| EP4314187A1 (en) | 2021-03-26 | 2024-02-07 | PPG Industries Ohio Inc. | Coating compositions |
| DE102021113089B4 (de) * | 2021-05-20 | 2023-05-11 | Jomoo Kitchen & Bath Deutschland Gmbh | Sanitär-Einrichtung |
| MX2024006742A (es) | 2021-12-02 | 2024-06-19 | Ppg Ind Ohio Inc | Composiciones de revestimiento. |
| CN114752334B (zh) * | 2022-04-11 | 2023-10-20 | 中国航发北京航空材料研究院 | 一种耐湿热贮存稳定的中温固化环氧结构胶膜及制备方法 |
| CA3252345A1 (en) | 2022-06-06 | 2023-12-14 | Ppg Industries Ohio, Inc. | COATING COMPOSITIONS |
| WO2024040260A1 (en) * | 2022-08-19 | 2024-02-22 | Ppg Industries Ohio, Inc. | Coating compositions |
| CN119968411A (zh) | 2022-08-22 | 2025-05-09 | Ppg工业俄亥俄公司 | 涂层组合物 |
| CN116042150A (zh) * | 2022-12-30 | 2023-05-02 | 浙江抟原复合材料有限公司 | 一种lng船围护系统用低温环氧树脂及其制备方法 |
| DE112024002400T5 (de) | 2023-06-01 | 2026-03-12 | Ppg Industries Ohio, Inc. | Zusammensetzungen, die thermisch leitfähige füllstoffe und thermisch expandierbare materialien enthalten |
| WO2025188361A2 (en) | 2023-11-19 | 2025-09-12 | Ppg Industries Ohio, Inc. | Curable compositions |
| WO2025183772A1 (en) | 2024-02-26 | 2025-09-04 | Ppg Industries Ohio, Inc. | Compositions containing a thermally conductive filler and a thermally expandable material |
| WO2025183769A1 (en) | 2024-02-26 | 2025-09-04 | Ppg Industries Ohio, Inc. | Furan-functional and isocyanate-functional compounds and reversibly curable compositions |
| WO2025183770A1 (en) | 2024-02-26 | 2025-09-04 | Ppg Industries Ohio, Inc. | Compositions containing furan-functional and isocyanate-functional compounds and expandable material |
| WO2025183771A1 (en) | 2024-02-26 | 2025-09-04 | Ppg Industries Ohio, Inc. | Compositions containing a thermally conductive filler and a thermally expandable material |
| WO2026059637A2 (en) | 2024-09-03 | 2026-03-19 | Ppg Industries Ohio, Inc. | Coating compositions and solvent-assisted degradable coatings formed therefrom |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3816365A (en) * | 1968-09-12 | 1974-06-11 | Ciba Geigy Ag | Adducts,containing epoxide groups,from polyglycidyl compounds and acid polyesters of aliphatic-cycloaliphatic dicarboxylic acids,process for their manufacture and use |
| US4668736A (en) * | 1984-07-18 | 1987-05-26 | Minnesota Mining And Manufacturing Company | Fast curing epoxy resin compositions |
| EP0305331A3 (de) * | 1987-08-25 | 1991-05-08 | Ciba-Geigy Ag | Epoxidflexibilisatoren |
| US5070119A (en) * | 1990-09-28 | 1991-12-03 | Ppg Industries, Inc. | Flexible intumescent coating composition |
| DE4317470C2 (de) * | 1993-05-26 | 2001-06-07 | Henkel Kgaa | Thermisch vernetzbarer Heißsiegel-Klebstoff und dessen Verwendung |
| JPH07309929A (ja) * | 1994-05-16 | 1995-11-28 | Dainippon Ink & Chem Inc | エポキシ樹脂及びその製造方法 |
| US7071258B1 (en) * | 2002-10-21 | 2006-07-04 | Nanotek Instruments, Inc. | Nano-scaled graphene plates |
| KR20040061909A (ko) * | 2002-12-31 | 2004-07-07 | 주식회사 금강고려화학 | 내후성 및 기계적 물성이 우수한 에폭시-폴리에스테르수지 조성과 분체 도료 조성물 |
| JP2006008730A (ja) * | 2004-06-22 | 2006-01-12 | Kyoeisha Chem Co Ltd | 油膜被覆鋼材と発泡した硬化エポキシ樹脂充填材との接着性の増強剤 |
| ES2691528T3 (es) * | 2006-07-31 | 2018-11-27 | Henkel Ag & Co. Kgaa | Composiciones adhesivas basadas en resina epoxi curable |
| BRPI0809752B1 (pt) * | 2007-04-11 | 2017-05-16 | Dow Global Technologies Inc | "adesivo estrutural de um componente e método" |
| KR20100059818A (ko) * | 2007-07-26 | 2010-06-04 | 헨켈 코포레이션 | 경화성 에폭시 수지계 접착제 조성물 |
| CN102102001B (zh) * | 2010-12-03 | 2013-04-17 | 烟台德邦科技有限公司 | 一种高导热石墨烯基环氧树脂胶粘剂及其制备方法 |
-
2011
- 2011-12-09 US US13/315,518 patent/US20120129980A1/en not_active Abandoned
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2012
- 2012-12-07 RU RU2014127905/04A patent/RU2595040C2/ru active
- 2012-12-07 EP EP12809911.6A patent/EP2788397A2/en active Pending
- 2012-12-07 SG SG11201403003SA patent/SG11201403003SA/en unknown
- 2012-12-07 WO PCT/US2012/068378 patent/WO2013086277A2/en not_active Ceased
- 2012-12-07 CA CA2858186A patent/CA2858186C/en active Active
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- 2012-12-07 IN IN4651DEN2014 patent/IN2014DN04651A/en unknown
- 2012-12-07 AU AU2012347650A patent/AU2012347650B2/en not_active Ceased
- 2012-12-07 MX MX2014006899A patent/MX380981B/es unknown
- 2012-12-07 CN CN201280067282.6A patent/CN104053694B/zh active Active
- 2012-12-07 KR KR1020147018721A patent/KR101684752B1/ko active Active
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| KR101684752B1 (ko) | 2016-12-08 |
| MX2014006899A (es) | 2015-05-15 |
| CN104053694A (zh) | 2014-09-17 |
| CA2858186A1 (en) | 2013-06-13 |
| RU2595040C2 (ru) | 2016-08-20 |
| MX380981B (es) | 2025-03-12 |
| US20120129980A1 (en) | 2012-05-24 |
| BR112014013594A8 (pt) | 2017-06-13 |
| CN104053694B (zh) | 2016-08-17 |
| CA2858186C (en) | 2016-06-07 |
| RU2014127905A (ru) | 2016-02-10 |
| AU2012347650A1 (en) | 2014-06-26 |
| EP2788397A2 (en) | 2014-10-15 |
| AU2012347650B2 (en) | 2015-09-17 |
| WO2013086277A3 (en) | 2013-08-15 |
| IN2014DN04651A (https=) | 2015-04-03 |
| SG11201403003SA (en) | 2014-07-30 |
| KR20140101838A (ko) | 2014-08-20 |
| WO2013086277A2 (en) | 2013-06-13 |
| BR112014013594A2 (pt) | 2017-06-13 |
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Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 07/12/2012, OBSERVADAS AS CONDICOES LEGAIS. |