| 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 | 包含马来酸酐与不饱和化合物和胺的反应产物的水性涂料组合物 | CN201380047245.3 | 2013-09-19 | CN104937043A | 2015-09-23 | G·P·克劳恩; J·T·拉德马赫; P·格伦 |
| 本发明包括具有取代琥珀酰亚胺化合物的水性涂料组合物，其中取代琥珀酰亚胺化合物具有至少约30mg KOH/g取代琥珀酰亚胺化合物的酸值。取代琥珀酰亚胺化合物可以为包含至少一个非芳族不饱和碳-碳键的不饱和油、衍生自不饱和油的聚合物或其组合与马来酸酐和伯胺的反应产物。 | ||||||
| 2 | 可固化组合物及其涂覆制品的方法及所得制品 | CN93114363.2 | 1993-11-11 | CN1036270C | 1997-10-29 | M·L·古尔德; D·A·格里; M·L·德特罗夫; R·A·希金尼; J·A·拉本 |
| 共反应树脂和含有中心部分和一个以上的非环酸酐部分的聚酐的组合物，经过固化得到具有良好的外部耐久性的涂层。优选的高分子量聚酐含有中心聚合物部分，后者具有不高于25wt%的得自不饱和脂族烃单体的重复单元。在其它优选聚酐中，酸酐部分通过酯部分键合到中心部分上。 | ||||||
| 3 | 聚酐、其制备方法、在防污涂料中的应用及包含聚酐的防污涂料 | CN200480011648.3 | 2004-04-23 | CN100351325C | 2007-11-28 | 阿妮塔·博尔韦; 马里特·达林格; 英厄雷敦·F·艾于克吕斯特; 拉斯洛·拉科什; 西伦·M·内塞特 |
| 本发明涉及通式为-(A)a-(B)b-(C)c-的新聚酐，制备新聚酐的方法，新聚酐在涂料中的应用及包含新聚酐的涂料。 | ||||||
| 4 | 聚酐、其制备方法、在防污涂料中的应用及包含聚酐的防污涂料 | CN200480011648.3 | 2004-04-23 | CN1780885A | 2006-05-31 | 阿妮塔·博尔韦; 马里特·达林格; 英厄雷敦·F·艾于克吕斯特; 拉斯洛·拉科什; 西伦·M·内塞特 |
| 本发明涉及通式为－(A)a－(B)b－(C)c－的新聚酐，制备新聚酐的方法，新聚酐在涂料中的应用及包含新聚酐的涂料。 | ||||||
| 5 | 涂覆制品的方法及所用的聚酐 | CN97102012.4 | 1993-11-11 | CN1167130A | 1997-12-10 | M·L·古尔德; D·A·格里; M·L·德特罗夫 |
| 共反应树脂和含有中心部分和一个以上的非环酸酐部分的聚酐的组合物，经过固化得到具有良好的外部耐久性的涂层。优选的高分子量聚酐含有中心聚合物部分，后者具有不高于25ωt％的得自不饱和脂族烃单体的重复单元。在其它优选聚酐中，酸酐部分通过酯部分键合到中心部分上。 | ||||||
| 6 | 可固化组合物和用于这种组合物的酸酐以及涂覆制品 | CN93114363.2 | 1993-11-11 | CN1087652A | 1994-06-08 | M·L·古尔德; D·A·格里; M·L·德特罗夫; R·A·希金尼; J·A·拉本 |
| 共反应树脂和含有中心部分和一个以上的非环酸酐部分的聚酐的组合物，经过固化得到具有良好的外部耐久性的涂层。优选的高分子量聚酐含有中心聚合物部分，后者具有不高于25wt％的得自不饱和脂族烃单体的重复单元。在其它优选聚酐中，酸酐部分通过酯部分键合到中心部分上。 | ||||||
| 7 | Aqueous Coating Compositions Including The Reaction Product Of Maleic Anhydride With An Unsaturated Compound And An Amine | US14428523 | 2013-09-19 | US20150247061A1 | 2015-09-03 | Gary Pierce Craun; Jude Rademacher; Patricia Geelen |
| The invention includes an aqueous coating composition having a substituted succinimide compound, wherein the substituted succinimide compound has an acid value of at least about 30 mg KOH/g of the substituted succinimide compound. The substituted succinimide compound may be the reaction product of an unsaturated oil comprising at least one non-aromatic unsaturated carbon-carbon bond, a polymer derived from the unsaturated oil, or a combination thereof with maleic anhydride and a primary amine. | ||||||
| 8 | Substrate coated with composition of non-cyclic polyanhydride and polyglycidyl oligomer | US790650 | 1997-01-29 | US5698641A | 1997-12-16 | Michael L. Gould; Marvin L. Dettloff; David A. Grilli; Richard A. Hickner; James A. Rabon |
| A coating composition applied to a substrate wherein the composition contains a solids content of at least about 65 percent by weight and includes a polyanhydride having more than one non-cyclic anhydride moiety, a glycidyl groups-containing oligomer, a catalyst and a surfactant or flow-control agent. | ||||||
| 9 | Quick-hardening coating composition | US820897 | 1992-01-24 | US5225519A | 1993-07-06 | Antonio Tortolina |
| Described is a coating composition comprising at least a polycarbodiimide component having at least two carbodiimide groups per molecule, at least one anhyride component having one or more carboxylic acid anhydride groups per molecule, and a hydroxylic reagent capable of reacting with said anhydride component to generate free carboxylic polyacids, at least one among said components and reagents being a compound suitable for forming films. The composition produces fast cross-linking coatings at low temperatures. | ||||||
| 10 | Pretreatment liquid, oil-based ink jet printing ink set, and oil-based ink jet printing method | US15412584 | 2017-01-23 | US09944820B2 | 2018-04-17 | Shigemi Wakabayashi |
| A pretreatment liquid for an oil-based ink contains one of a maleic anhydride resin derivative and an aluminum chelate compound. | ||||||
| 11 | Antimicrobial polyanhydride nanoparticles | US13866520 | 2013-04-19 | US08927024B1 | 2015-01-06 | Bryan Bellaire; Balaji Narasimhan |
| The invention provides compositions and methods to treat microbial infections in animals, to inhibit the replication of microbes in infected cells, and to kill pathogens in infected cells. The methods can include administering to an animal in need of such treatment an effective antimicrobial amount of a composition comprising polyanhydride microparticles or nanoparticles that encapsulate a plurality of antimicrobial agents. The polyanhydride microparticles or nanoparticles can be, for example, copolymers of sebacic anhydride (SA) and 1,6-bis-(p-carboxyphenoxy)hexane (CPH) anhydride, copolymers of 1,8-bis(carboxyphenoxy)-3,6-dioxaoctane (CPTEG) anhydrides and 1,6-bis-(p-carboxyphenoxy)hexane (CPH) anhydride, or various combinations thereof. The microparticles or nanoparticles can accumulate in infected monocytes, dendritic cells, both, or on or in other infected cells, and degrade by surface erosion over a period of time to release the antimicrobial agents, thereby killing or inhibiting the microbes and treating the infection. | ||||||
| 12 | Antimicrobial compositions and methods | US12940872 | 2010-11-05 | US08449916B1 | 2013-05-28 | Bryan Bellaire; Balaji Narasimhan |
| The invention provides compositions and methods to treat microbial infections in animals, to inhibit the replication of microbes in infected cells, and to kill pathogens in infected cells. The methods can include administering to an animal in need of such treatment an effective antimicrobial amount of a composition comprising polyanhydride microparticles or nanoparticles that encapsulate a plurality of antimicrobial agents. The polyanhydride microparticles or nanoparticles can be, for example, copolymers of sebacic anhydride (SA) and 1,6-bis-(p-carboxyphenoxy)hexane (CPH) anhydride, copolymers of 1,8-bis(carboxyphenoxy)-3,6-dioxaoctane (CPTEG) anhydrides and 1,6-bis-(p-carboxyphenoxy)hexane (CPH) anhydride, or various combinations thereof. The microparticles or nanoparticles can accumulate in infected monocytes, dendritic cells, both, or on or in other infected cells, and degrade by surface erosion over a period of time to release the antimicrobial agents, thereby killing or inhibiting the microbes and treating the infection. | ||||||
| 13 | Coating composition of non-cyclic polyanhydride and co-reactant resin | US539138 | 1995-10-04 | US5633020A | 1997-05-27 | Michael L. Gould; David A. Grilli; Marvin L. Dettloff; Richard A. Hickner; James A. Rabon |
| A coating composition with a solids content of at least about 65% by weight comprises a polyanhydride having more than one non-cyclic anhydride moiety, a co-reactant resin such as a glycidyl (meth)acrylate-containing polymer and a latent catalyst wherein the equivalent ratio of epoxy to anhydride is from about 0.8:1 to 1.3:1. | ||||||
| 14 | Rapid curing of the coating composition | JP50793190 | 1990-05-22 | JP3191874B2 | 2001-07-23 | トルトリーナ，アントニオ |
| 15 | USE OF POLYANHYDRIDES IN ANTIFOULING PAINT AND ANTIFOULING PAINT CONTAINING POLYANHYDRIDES | EP04729326.1 | 2004-04-23 | EP1618157B1 | 2007-03-14 | BÖRVE, Anita; DAHLING, Marit; AUKRUST, Inger Reidun F.; RAKOS, Laszlo; NESET, Siren M. |
| The invention concerns novel polyanhydrides with the general formula -(A)a - (B)b - (C)c -, a method for preparation of the novel anhydrides, use of the novel anhydrides in paint and a paint containing the novel anhydrides. | ||||||
| 16 | PRETREATMENT LIQUID, OIL-BASED INK JET PRINTING INK SET, AND OIL-BASED INK JET PRINTING METHOD | US15412584 | 2017-01-23 | US20170210941A1 | 2017-07-27 | Shigemi WAKABAYASHI |
| A pretreatment liquid for an oil-based ink contains one of a maleic anhydride resin derivative and an aluminum chelate compound. | ||||||
| 17 | Aqueous coating compositions including the reaction product of maleic anhydride with an unsaturated compound and an amine | US14428523 | 2013-09-19 | US09469785B2 | 2016-10-18 | Gary Pierce Craun; Jude Rademacher; Patricia Geelen |
| The invention includes an aqueous coating composition having a substituted succinimide compound, wherein the substituted succinimide compound has an acid value of at least about 30 mg KOH/g of the substituted succinimide compound. The substituted succinimide compound may be the reaction product of an unsaturated oil comprising at least one non-aromatic unsaturated carbon-carbon bond, a polymer derived from the unsaturated oil, or a combination thereof with maleic anhydride and a primary amine. | ||||||
| 18 | Substrate coated with composition of non-cyclic polyanhydride and co-reactant resin | US790649 | 1997-01-29 | US5698332A | 1997-12-16 | Michael L. Gould; David A. Grilli; Marvin L. Dettloff; Richard A. Hickner; James A. Rabon |
| A coating composition applied to a substrate, the composition containing a solids content of at least about 65 percent by weight and including a polyanhydride having more than one non-cyclic moiety, a co-reactant resin such as a glycidyl (meth)acrylate-containing polymer, and a latent catalyst, wherein the equivalent ratio of epoxy to anhydride groups is from about 0.8:1 to 1.3:1. | ||||||
| 19 | Coating composition of non-cyclic polyanhydride and glycidyl oligomer | US539137 | 1995-10-04 | US5633330A | 1997-05-27 | Michael L. Gould; David A. Grilli; Marvin L. Dettloff; Richard A. Hickner; James A. Rabon |
| A coating composition with a solids content of at least about 65% by weight comprises a polyanhydride having more than one non-cyclic anhydride moiety, a glycidyl groups-containing oligomer, a catalyst and a surfactant or flow-control agent. | ||||||
| 20 | Polyanhydride containing non-cyclic anhydride moieties | US396458 | 1995-02-28 | US5602274A | 1997-02-11 | Michael L. Gould; David A. Grilli; Marvin L. Dettloff; Richard A. Hickner; James A. Rabon |
| A polyanhydride having a molecular weight of no more than about 2000 is useful in a coating composition with a coreactant resin such as an epoxy resin and comprises:(a) a polyvalent organic moiety;(b) a plurality of ester linkages bonded to the polyvalent organic moiety;(c) divalent organic moieties bonded to the ester linkages; and(d) non-cyclic anhydride moleties bonded to the divalent organic moleties. | ||||||
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