| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 皮革涂料粘合剂和良好压花性及耐湿弯曲性的涂覆皮革 | CN00101098.0 | 2000-01-19 | CN1229456C | 2005-11-30 | P·M·莱斯科; F·J·欣德勒 |
| 本发明提供了一种含水皮革涂料组合物、以及一种用该含水涂料组合物涂覆皮革的方法。该含水涂料组合物包含一种含水乳液聚合物，该乳液聚合物包含0.4-10%重量的共聚乙酰乙酸酯或乙酰乙酰胺单体且其玻璃化转变温度(Tg)为-20℃至10℃。在另一实施方案中，该含水涂料组合物包含一种含水乳液聚合物，该乳液聚合物包含0.1-6%重量的共聚乙酰乙酸酯或乙酰乙酰胺单体和2-15%重量的共聚羧酸单体且其玻璃化转变温度(Tg)为-40℃至0℃；所述聚合物已与过渡金属氧化物、氢氧化物、或碳酸盐在低于9的pH值下接触，过渡金属的量超过0.20当量/聚合物中的每当量共聚羧酸单体。 | ||||||
| 2 | 皮革涂料粘合剂和良好压花性及耐湿弯曲性的涂覆皮革 | CN200510079145.6 | 2000-01-19 | CN1699490A | 2005-11-23 | P·M·莱斯科; F·J·欣德勒 |
| 本发明提供了一种含水皮革涂料组合物、以及一种用该含水涂料组合物涂覆皮革的方法。该含水涂料组合物包含一种含水乳液聚合物，该乳液聚合物包含0.4－10％重量的共聚乙酰乙酸酯或乙酰乙酰胺单体且其玻璃化转变温度(Tg)为－20℃至10℃。在另一实施方案中，该含水涂料组合物包含一种含水乳液聚合物，该乳液聚合物包含0.1－6％重量的共聚乙酰乙酸酯或乙酰乙酰胺单体和2－15％重量的共聚羧酸单体且其玻璃化转变温度(Tg)为－40℃至0℃；所述聚合物已与过渡金属氧化物、氢氧化物、或碳酸盐在低于9的pH值下接触，过渡金属的量超过0.20当量/聚合物中的每当量共聚羧酸单体。 | ||||||
| 3 | 皮革涂料粘合剂和良好压花性及耐湿弯曲性的涂覆皮革 | CN200510079145.6 | 2000-01-19 | CN100393830C | 2008-06-11 | P·M·莱斯科; F·J·欣德勒 |
| 本发明提供了一种含水皮革涂料组合物、以及一种用该含水涂料组合物涂覆皮革的方法。该含水涂料组合物包含一种含水乳液聚合物，该乳液聚合物包含0.4-10%重量的共聚乙酰乙酸酯或乙酰乙酰胺单体且其玻璃化转变温度(Tg)为-20℃至10℃。在另一实施方案中，该含水涂料组合物包含一种含水乳液聚合物，该乳液聚合物包含0.1-6%重量的共聚乙酰乙酸酯或乙酰乙酰胺单体和2-15%重量的共聚羧酸单体且其玻璃化转变温度(Tg)为-40℃至0℃；所述聚合物已与过渡金属氧化物、氢氧化物、或碳酸盐在低于9的pH值下接触，过渡金属的量超过0.20当量/聚合物中的每当量共聚羧酸单体。 | ||||||
| 4 | 含有稀丙醚单体的可交联分散性树脂粘合剂 | CN03811486.0 | 2003-03-10 | CN1656185A | 2005-08-17 | M·梅尔希奥斯; R·格尔茨曼; S·哈克巴斯; R·皮尔斯 |
| 本发明涉及含水可交联且含有基于乙二醇单烯丙醚的羟基官能团共聚物的粘合剂分散体，制备该分散体的方法和该分散体在涂漆中的应用。 | ||||||
| 5 | 含有氨基甲酸酯和丙烯酰胺官能组分的涂层组合物 | CN95120873.X | 1995-12-20 | CN1064388C | 2001-04-11 | J·D·麦克吉; B·D·巴麦尔; J·W·里福斯 |
| 一种涂层组合物包括含有带有多于一个氨基甲酸酯官能基的化合物的组分，及能与所述氨基甲酸酯基团反应的另一组分，该组分为取代的丙烯酰胺化合物。此组合物在着色加透明复合涂层中用作透明涂层组合物。 | ||||||
| 6 | 皮革涂料粘合剂和良好压花性及耐湿弯曲性的涂覆皮革 | CN00101098.0 | 2000-01-19 | CN1262298A | 2000-08-09 | P·M·莱斯科; F·J·欣德勒 |
| 本发明提供了一种含水皮革涂料组合物、以及一种用该含水涂料组合物涂覆皮革的方法。该含水涂料组合物包含一种含水乳液聚合物,该乳液聚合物包含0.4—10%重量的共聚乙酰乙酸酯或乙酰乙酰胺单体且其玻璃化转变温度(Tg)为－20℃至10℃。在另一实施方案中,该含水涂料组合物包含一种含水乳液聚合物,该乳液聚合物包含0.1—6%重量的共聚乙酰乙酸酯或乙酰乙酰胺单体和2—15%重量的共聚羧酸单体且其玻璃化转变温度(Tg)为－40℃至0℃;所述聚合物已与过渡金属氧化物、氢氧化物、或碳酸盐在低于9的pH值下接触,过渡金属的量超过0.20当量/聚合物中的每当量共聚羧酸单体。 | ||||||
| 7 | 含有氨基甲酸酯和丙烯酰胺功能组分的涂层组合物 | CN95120873.X | 1995-12-20 | CN1133330A | 1996-10-16 | J·D·麦克吉; B·D·巴麦尔; J·W·里福斯 |
| 一种涂层组合物包括含有带有多于一个氨基甲酸酯功能基的化合物的组分，及能与所述氨基甲酸酯基团反应的另一组分，该组分为取代的丙烯酰胺化合物。此组合物在加色透明复合涂层中用作透明涂层组合物。 | ||||||
| 8 | 안정한 신규 수성 하이브리드 결합제 | KR1020147008523 | 2011-10-21 | KR1020140080491A | 2014-06-30 | 왕유이장; 휴지안밍; 무카말라래비 |
| 본 발명은 변형 없이 간단히 가공되는 안정한 신규 콜로이드성 실리카 함유 폴리머성 결합제, 및 합리적이면서 관리가능한 비용으로 더욱 효율적인 오염 저항성/제거 기능을 가지는 신규 코팅 조성물, 특히, 수성 코팅 조성물을 제공한다. | ||||||
| 9 | 알릴 에테르 모노머를 함유하는 가교형 수지 결합제분산액 | KR1020047014779 | 2003-03-10 | KR1020050007443A | 2005-01-18 | 멜키오르스,마르틴; 게르츠만,롤프; 하크바르트,잔드라; 피레스,라울 |
| 본 발명은 에틸렌 글리콜 모노알릴 에테르를 기재로 한 히드록시 관능성 공중합체를 포함하는 가교형 결합제 수분산액, 이의 제조 방법 및 상기 분산액의 코팅 물질에서의 용도에 관한 것이다. | ||||||
| 10 | 카르바메이트작용성성분및아크릴아미드작용성성분을포함하는코팅조성물 | KR1019950053039 | 1995-12-20 | KR100348367B1 | 2005-01-25 | 존디.맥기; 브라이언디.바멜; 존더블유.레푸스 |
| A coating composition including a first component comprising a compound having appended thereto more than one carbamate functional group, and further including a second component reactive with said carbamate groups, which is a substituted acrylamide compound. The composition is useful as a clearcoating composition in a color-plus-clear composite coating. | ||||||
| 11 | 경화성조성물,이의적용방법및폴리(C1-C6알킬아크릴아미도글리콜레이트)관능성중합체의제조방법 | KR1019860009968 | 1986-11-24 | KR1019930004057B1 | 1993-05-19 | 하워드로버트루카스; 로버트제럴드리이즈; 허버트버크하아드; 데이빗드아아서리이 |
| 내용 없음. | ||||||
| 12 | 가죽 코팅 바인더 및 우수한 엠보싱력과 습-유연 내구성을갖는 코팅된 가죽 | KR1020000001459 | 2000-01-13 | KR1020000062458A | 2000-10-25 | 레스코페트리시아마리; 쉰들러프레드릭제임스 |
| 수성가죽코팅조성물및 수성가죽코팅조성물을이용한가죽코팅방법이제공된다. 상기수성코팅조성물은공중합된아세토아세테이트또는아세토아세트아미드단량체 0.4~10중량%를포함하며 -20℃에서 10℃의유리전이온도(Tg)를갖는수성에멀젼중합체를포함한다. 다른구체화에서, 상기수성코팅조성물은공중합된아세토아세테이트또는아세토아세트아미드단량체 0.1~6중량%, 공중합된카르복실산단량체 2~15중량%를포함하며 -40℃에서 0℃의유리전이온도를갖는수성에멀젼중합체를포함한다. 여기서상기중합체는공중합된카르복시산당량당전이금속이 0.20 당량이되도록 pH9 미만에서전이금속산화물, 수산화물또는카보네이트와접촉된다. | ||||||
| 13 | 열경화성조성물, 열잠재성산촉매, 도장마무리방법 및 도장물품, 그리고 성형방법 및 성형품 | KR1019940022292 | 1994-09-06 | KR100156289B1 | 1998-12-01 | 나카네요시노리; 미즈타니히로키; 이시바시하야토; 이시도야마사히로 |
| 본 발명은, (A)1분자속에, 하기의 일반식(1)의 특정의 화합물로 블록화된 카르복실기로 이루어진 작용기 2개이상을 가진 화합물, (B)1분자속에, 상기 작용기와 가열에 의해 화학결합을 형성할 수 있는 반응성 작용기 2개이상을 가진 화합물, 또는 (D)1분자속에 (A)의 블록화된 카르복실기 1개이상과 (B)의 작용기 1개이상을 가진 자체가교형 화합물과, (C)에폭시기를 함유하는 화합물, 특정의 함유황화합물 및 특정의 루이스산으로 이루어진 열잠재성산촉매를 필수성분으로서 함유해서 이루어진 열경화성 조성물, 그에 의한 도장방법 및 도장물품 그리고 성형방법 및 성형품에 관한 것으로, 또 (A) 및 (B), 또는 (D)와 (C)산촉매를 필수성분으로서 함유해서 이루어지고, 또한 휘발성 유기화합물을 희석제로서 실질적으로 사용하지 않는 것을 특징으로 하는 열경화성� �성물, 그에 의한 도장방법 및 도장물품 그리고 성형방법 및 성형품으로서, 화학성능, 물리성능, 또는 내후성, 내오염성등이 뛰어난 경화물을 부여하는 효과를 가진다. | ||||||
| 14 | 도장법 | KR1019870011906 | 1987-10-26 | KR1019950009547B1 | 1995-08-24 | 구와지마데루아끼; 우에노야마가즈오; 다까에마사끼; 오꾸다히데후미 |
| 내용 없음. | ||||||
| 15 | Crosslinkable binder dispersions | US10391169 | 2003-03-18 | US07022760B2 | 2006-04-04 | Martin Melchiors; Rolf Gertzmann; Sandra Grosskopf; Raul Pires |
| The invention relates to aqueous crosslinkable binder dispersions comprising hydroxy-functional copolymers based on ethylene glycol monoallyl ether, to a process for preparing them and to the use of the dispersions in coating materials. | ||||||
| 16 | Leather coating binder and coated leather having good embossability and wet-flex endurance | US09870576 | 2001-05-31 | US06387291B2 | 2002-05-14 | Patricia Marie Lesko; Frederick James Schindler |
| An aqueous leather coating composition and a method for coating leather with the aqueous coating composition are provided. The aqueous coating composition contains an aqueous emulsion polymer which includes from 0.4% to 10% by weight of a copolymerized acetoacetate or acetoacetamide monomer and has a glass transition temperature from −20° C. to 10° C. In an alternative embodiment the aqueous coating composition contains an aqueous emulsion polymer which includes from 0.1% to 6% by weight of a copolymerized acetoacetate or acetoacetamide monomer and from 2% to 15% by weight of copolymerized carboxylic acid monomer and has a glass transition temperature from −40° C. to 0° C., the polymer having been contacted with a transition metal oxide, hydroxide, or carbonate at a pH less than 9 in an amount greater than 0.20 equivalent of transition metal per equivalent of copolymerized carboxylic acid monomer. | ||||||
| 17 | Leather coating binder and coated leather having good embossability and wet-flex endurance | US09870576 | 2001-05-31 | US20010038085A1 | 2001-11-08 | Patricia Marie Lesko; Frederick James Schindler |
| An aqueous leather coating composition and a method for coating leather with the aqueous coating composition are provided. The aqueous coating composition contains an aqueous emulsion polymer which includes from 0.4% to 10% by weight of a copolymerized acetoacetate or acetoacetamide monomer and has a glass transition temperature from null20null C. to 10null C. In an alternative embodiment the aqueous coating composition contains an aqueous emulsion polymer which includes from 0.1% to 6% by weight of a copolymerized acetoacetate or acetoacetamide monomer and from 2% to 15% by weight of copolymerized carboxylic acid monomer and has a glass transition temperature from null40null C. to 0null C., the polymer having been contacted with a transition metal oxide, hydroxide, or carbonate at a pH less than 9 in an amount greater than 0.20 equivalent of transition metal per equivalent of copolymerized carboxylic acid monomer. | ||||||
| 18 | Leather coating binder and coated leather having good embossability and wet-flex endurance | US09480204 | 2000-01-10 | US06290866B1 | 2001-09-18 | Patricia Marie Lesko; Frederick James Schindler |
| An aqueous leather coating composition and a method for coating leather with the aqueous coating composition are provided. The aqueous coating composition contains an aqueous emulsion polymer which includes from 0.4% to 10% by weight of a copolymerized acetoacetate or acetoacetamide monomer and has a glass transition temperature from −20° C. to 10° C. In an alternative embodiment the aqueous coating composition contains an aqueous emulsion polymer which includes from 0.1% to 6% by weight of a copolymerized acetoacetate or acetoacetamide monomer and from 2% to 15% by weight of copolymerized carboxylic acid monomer and has a glass transition temperature from −40° C. to 0° C., the polymer having been contacted with a transition metal oxide, hydroxide, or carbonate at a pH less than 9 in an amount greater than 0.20 equivalent of transition metal per equivalent of copolymerized carboxylic acid monomer. | ||||||
| 19 | (Meth)acrylate copolymer based UV-crosslinkable materials | US88736 | 1993-07-08 | US5389699A | 1995-02-14 | Gerd Rehmer; Andreas Boettcher; Michael Portugall |
| UV-crosslinkable materials based on (meth)acrylate copolymers and containing from 0.01 to 10% by weight, based on the copolymer, of copolymerized monomers of the formula I ##STR1## where x is alkyl of 1 to 3 carbon atoms or is phenyl which is unsubstituted or substituted by n Y groups, Y is --H, --CF.sub.3, --O-- alkyl and/or alkyl-COO--, where alkyl in each case is of 1 to 4 carbon atoms, halogen, --CH, --COOH or a non-ortho --OH group, n is from 0 to 4 and Z is a group of the formula ##STR2## where R is H or C.sub.1 -C.sub.4 -alkyl and A is an alkylene, oxaalkylene or polyoxaalkylene radical of 2 to 12 carbon atoms are used as hotmelt adhesives, for coating sheet-like mineral substrates and as surface coatings. | ||||||
| 20 | Benzophenone derivatives and their preparation | US742163 | 1991-08-01 | US5264533A | 1993-11-23 | Gerd Rehmer; Andreas Boettcher; Michael Portugall |
| UV-crosslinkable materials based on (meth)acrylate copolymers and containing special modified unsaturated benzophenone derivatives as copolymerized units are used as hotmelt adhesives, for coating sheet-like mineral substrates and as surface coatings. | ||||||
QQ群二维码
意见反馈
意见反馈