KR20200057711A - 고강도의 긴 개방 시간을 가진 폴리우레탄 반응성 열 용융물 - Google Patents
고강도의 긴 개방 시간을 가진 폴리우레탄 반응성 열 용융물 Download PDFInfo
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- KR20200057711A KR20200057711A KR1020207008055A KR20207008055A KR20200057711A KR 20200057711 A KR20200057711 A KR 20200057711A KR 1020207008055 A KR1020207008055 A KR 1020207008055A KR 20207008055 A KR20207008055 A KR 20207008055A KR 20200057711 A KR20200057711 A KR 20200057711A
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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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/08—Polyurethanes from polyethers
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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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/06—Polyurethanes from 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
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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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- C08G18/4018—Mixtures of compounds of group C08G18/42 with compounds of group C08G18/48
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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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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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Abstract
화학식 1은:
여기서, m과 n은 각각 짝수의 정수이고; m+n=8이고; m과 n은 각각 2, 4, 또는 6으로부터 독립적으로 선택되고; k는 9 내지 55의 정수이고; 화학식 1의 폴리올은 약 2,000 내지 약 11,000의 수 평균 분자량을 갖는다. 화학식 2, 폴리카프로락톤 폴리올은:
여기서, R1은 1,4'-부탄디올, 1,6'-헥산디올, 또는 에틸렌 글리콜과 같은 개시제이고; p는 0 내지 96의 정수이고; q는 0 내지 96의 정수이고; p+q=16 내지 96이고; 폴리올은 약 2,000 내지 약 11,000의 수 평균 분자량을 갖는다.
Description
Claims (20)
- 폴리이소시아네이트, 적어도 하나의 폴리에테르 폴리올 중합체, 아크릴 중합체, 무기 충전제, 및 하기 화학식 1 또는 화학식 2의 구조를 갖는 폴리에스테르 디올을 포함하는 혼합물의 생성물인 수분 반응성 열 용융 접착제 조성물:
<화학식 1>
(여기서, m과 n은 각각 짝수의 정수이고; m+n=8이고; m과 n은 각각 2, 4, 또는 6으로부터 독립적으로 선택되고; k는 9 내지 55의 정수이고; 화학식 1의 폴리올은 약 2,000 내지 약 11,000의 수 평균 분자량을 갖는다)
<화학식 2>
(여기서, Ri는 개시제이고; p는 0 내지 96의 정수이고; q는 0 내지 96의 정수이고; p+q=16 내지 96이고; 폴리올은 약 2,000 내지 약 11,000의 수 평균 분자량을 갖는다). - 제1항에 있어서, Ri이 1,4'-부탄디올, 1,6'-헥산디올, 에틸렌 글리콜 및 이들의 조합으로부터 선택된 글리콜 개시제의 잔기인 수분 반응성 열 용융 접착제 조성물.
- 제1항 또는 제2항에 있어서, 폴리에스테르 폴리올이 2,000 내지 10,000의 수 평균 분자량을 가지며, 총 접착제 중량을 기준으로 10 내지 35 중량%의 양으로 존재하는 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제3항 중 어느 한 항에 있어서, 상기 폴리에테르 폴리올 중합체가 1,500 내지 6,000의 수 평균 분자량을 가지며, 총 접착제 중량을 기준으로 15 내지 40 중량%의 양으로 존재하는 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제4항 중 어느 한 항에 있어서, 상기 폴리에테르 폴리올 중합체가 적어도 하나의 폴리프로필렌 글리콜을 포함하는 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제5항 중 어느 한 항에 있어서, 상기 아크릴 중합체가 30,000 내지 80,000의 중량 평균 분자량을 가지며, 총 접착제 중량을 기준으로 10 내지 40 중량%의 양으로 존재하는 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제6항 중 어느 한 항에 있어서, 상기 아크릴 중합체가 35 내지 85 ℃의 유리 전이 온도 및 8 미만의 히드록실가를 갖는 것인 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제7항 중 어느 한 항에 있어서, 상기 폴리이소시아네이트가 총 접착제 중량을 기준으로 5 내지 40 중량%의 양으로 존재하는 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제8항 중 어느 한 항에 있어서, 상기 폴리이소시아네이트가 4,4'-메틸렌비스페닐디이소시아네이트를 포함하는 것인 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제9항 중 어느 한 항에 있어서, 상기 무기 충전제가 총 접착제 중량을 기준으로 약 10 내지 50 중량%의 양으로 존재하는 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제10항 중 어느 한 항에 있어서, 상기 무기 충전제가 탄산칼슘을 포함하는 것인 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제11항 중 어느 한 항에 있어서, 추가적 충전제, 가소제, 촉매, 착색제, 레올로지 조절제, 난연제, UV 색소, 나노섬유, 소포제, 점착부여제, 경화 촉매, 항산화제, 접착 촉진제, 안정화제, 틱소트로픽제 및 이들의 혼합물 중 선택된 첨가제를 더 포함하는 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제12항 중 어느 한 항에 있어서, 총 조성물 중량을 기준으로 0.02 내지 0.5 중량%의 2,2'-디모르폴리노디에틸에테르를 추가로 포함하는 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제13항 중 어느 한 항에 있어서, 6 내지 10 분의 개방 시간을 갖는 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제14항 중 어느 한 항에 있어서, 기재에 적용된 후 30 분 이내에 120 psi (평방 인치 당 파운드) 초과의 미처리 강도 (green strength)를 나타내는 수분 반응성 열 용융 접착제 조성물.
- 제1항 내지 제15항 중 어느 한 항에 따른 수분 반응성 열 용융 접착제 조성물을 포함하는 제조품.
- 제1항 내지 제15항 중 어느 한 항에 따른 열 용융 접착제를 용융된 형태로 제1 기재에 적용하고, 이어서 제2 기재를 제1 기재상의 접착제와 접촉시키고, 접착제를 냉각시키고 비가역적인 고체 형태로 경화시키는 것을 포함하는, 두 개의 기재를 함께 결합시키는 방법.
- 제1항 내지 제15항 중 어느 한 항에 따른 열 용융 접착제 조성물의 경화된 반응 생성물.
- 607 psi 이상의 항복 강도 및 1415 psi 이상의 인장 강도 중 적어도 하나를 갖는, 제1항 내지 제15항 중 어느 한 항에 따른 열 용융 접착제 조성물의 경화된 반응 생성물.
- 90 ℃에서의 저장 탄성률이 2.59 E+06 이상인, 제1항 내지 제15항 중 어느 한 항에 따른 열 용융 접착제 조성물의 경화된 반응 생성물.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762561786P | 2017-09-22 | 2017-09-22 | |
| US62/561,786 | 2017-09-22 | ||
| PCT/US2018/052121 WO2019060658A1 (en) | 2017-09-22 | 2018-09-21 | LONG-TIME OPEN AND HIGH-RESISTANCE POLYURETHANE REACTIVE THERMOFUSIBLE ADHESIVE |
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| WO2016139966A1 (ja) * | 2015-03-02 | 2016-09-09 | 旭硝子株式会社 | 粉体塗料用組成物、粉体塗料および塗装物品 |
| CA3190003A1 (en) * | 2020-08-14 | 2022-02-17 | Henkel Ag & Co. Kgaa | Polyurethane reactive hot melt with long pot-life under heat |
| AU2022214827A1 (en) * | 2021-01-28 | 2023-08-03 | Henkel Ag & Co. Kgaa | Process of incorporating gelling and phase separation inhibitor into a filled polyurethane reactive hot melt adhesive |
| CA3210665A1 (en) * | 2021-02-03 | 2022-08-11 | Henkel Ag & Co. Kgaa | Thermally stable filled polyurethane reactive hot melt |
| BR112023025740A2 (pt) | 2021-06-30 | 2024-02-27 | Dow Global Technologies Llc | Processo para formar uma composição, composição reticulada, primeira composição, e, artigo |
| CN113861826A (zh) * | 2021-10-22 | 2021-12-31 | 河南城建学院 | 一种环保型聚氨酯防水涂料 |
| KR20240132455A (ko) * | 2022-01-07 | 2024-09-03 | 헨켈 아게 운트 코. 카게아아 | 반응성 핫 멜트 접착제 조성물 및 그의 용도 |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4775719A (en) | 1986-01-29 | 1988-10-04 | H. B. Fuller Company | Thermally stable hot melt moisture-cure polyurethane adhesive composition |
| US5021507A (en) | 1986-05-05 | 1991-06-04 | National Starch And Chemical Investment Holding Corporation | Arcylic modified reactive urethane hot melt adhesive compositions |
| US4808255A (en) | 1987-05-07 | 1989-02-28 | H. B. Fuller Company | Thermally stable reactive hot melt urethane adhesive composition having a thermoplastic polymer, a compatible, curing urethane polyester polyol prepolymer and a tackifying agent |
| GB8810701D0 (en) | 1988-05-06 | 1988-06-08 | Bostik Ltd | Hot-melt polyurethane adhesive compositions |
| GB8826702D0 (en) | 1988-11-15 | 1988-12-21 | Bostik Ltd | Moisture-curing polyurethane hot-melt compositions |
| EP0576453A1 (de) | 1991-03-20 | 1994-01-05 | Henkel Kommanditgesellschaft auf Aktien | Schmelzklebstoff |
| US5866656A (en) | 1995-06-07 | 1999-02-02 | National Starch And Chemical Investment Holding Corporation | Polyurethane hotmelt adhesives with reactive acrylic copolymers |
| EP0764670A1 (en) * | 1995-09-25 | 1997-03-26 | Minnesota Mining And Manufacturing Company | Reactive hot-melt adhesive and/or sealing composition |
| JPH1036481A (ja) * | 1996-07-23 | 1998-02-10 | Dainippon Ink & Chem Inc | 一液湿気硬化型ウレタン組成物及び接着剤 |
| US6465104B1 (en) | 1997-12-01 | 2002-10-15 | Henkel Kommanditgesellschaft Auf Aktien | Modified polyurethane hotmelt adhesive |
| US6635722B2 (en) * | 2000-05-02 | 2003-10-21 | Henkel Corporation | Moisture-curable polyurethane hot melt adhesives containing reactive amine catalysts |
| US7025853B2 (en) * | 2002-07-03 | 2006-04-11 | Rohm And Haas Company | Reactive hot-melt adhesive compositions with improved green strength |
| JP2008500406A (ja) * | 2004-05-24 | 2008-01-10 | ナショナル スターチ アンド ケミカル インベストメント ホールディング コーポレーション | 新規な反応性ホットメルト接着剤 |
| JP2007211150A (ja) * | 2006-02-10 | 2007-08-23 | Oshika:Kk | 反応型ホットメルト接着剤組成物 |
| EP1997616B1 (en) | 2007-06-01 | 2009-08-26 | Sika Technology AG | Honeycomb sandwich panels and the use of a two component polyurethane adhesive in the manufacture thereof |
| JP2009286883A (ja) * | 2008-05-29 | 2009-12-10 | Sanyo Chem Ind Ltd | 反応性ホットメルト接着剤 |
| JP5734092B2 (ja) * | 2011-05-24 | 2015-06-10 | ヘンケルジャパン株式会社 | 湿気硬化型ホットメルト接着剤 |
| US9464155B2 (en) | 2012-04-12 | 2016-10-11 | Dic Corporation | Moisture-curable polyurethane hot-melt resin composition, adhesive, and article |
| CN103865465A (zh) | 2012-12-14 | 2014-06-18 | 江苏天顺新材料有限公司 | 汽车车灯用湿固化聚氨酯热熔胶及其制备方法 |
| EP2948487B1 (de) * | 2013-01-25 | 2021-07-28 | Henkel AG & Co. KGaA | Feuchtigkeitshärtende polyurethan-zusammensetzung enthaltend nachhaltig erzeugte rohstoffe |
| JP6196851B2 (ja) * | 2013-09-06 | 2017-09-13 | 積水フーラー株式会社 | 湿気硬化型ホットメルト接着剤 |
| WO2015045635A1 (ja) * | 2013-09-27 | 2015-04-02 | Dic株式会社 | 製本用接着剤 |
| EP2944662B1 (en) | 2014-05-16 | 2018-07-18 | Henkel AG & Co. KGaA | Thermoplastic polyurethane hot melt adhesive |
| JP6343547B2 (ja) * | 2014-10-29 | 2018-06-13 | 積水フーラー株式会社 | 湿気硬化型ホットメルト接着剤 |
| EP3313911A1 (en) * | 2015-06-29 | 2018-05-02 | Basf Se | Reactive hot melt adhesive |
| CA3006685A1 (en) * | 2015-12-18 | 2017-06-22 | Sika Technology Ag | One-part polyurethane adhesive with high green strength |
| WO2017108873A1 (de) | 2015-12-23 | 2017-06-29 | Sika Technology Ag | Polyurethan-schmelzklebstoff auf basis von polyacrylaten mit hohem wärmestand |
| JP2019508529A (ja) * | 2016-01-13 | 2019-03-28 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェンHenkel AG & Co. KGaA | 充填剤を含有する反応性ポリウレタンホットメルト接着剤 |
| CN114616304B (zh) * | 2019-10-30 | 2024-08-20 | 汉高股份有限及两合公司 | 用于低温施加的聚氨酯热熔粘合剂 |
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| US12275869B2 (en) | 2025-04-15 |
| RU2020114213A3 (ko) | 2022-04-29 |
| EP3684873B1 (en) | 2024-05-29 |
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