| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 61 | Radiation curable coating compositions for metal | US13976763 | 2011-12-23 | US09856392B2 | 2018-01-02 | Gary Pierce Craun; Kenneth James Gardner; Patricia Miller |
| Various embodiments of radiation curable coating compositions are provided. In one embodiment, a radiation curable coating composition includes a (meth)acrylate functional compound and an adhesion promoting (meth)acrylate compound. The radiation curable coating composition can also include a (meth)acrylate functional compound, a poly(meth)acrylate and a reactive diluent. The (meth)acrylate functional compound can be made from the reaction of a multifunctional isocyanate, a polyol and a hydroxyl functional (meth)acrylate in the presence of a catalyst. | ||||||
| 62 | COMPOSITION COMPRISING CYCLIC SECONDARY AMINE AND METHODS OF COATING DRINKING WATER PIPELINES | US15484260 | 2017-04-11 | US20170218224A1 | 2017-08-03 | Ryan B. Prince; Clinton L. Jones; Stuart E. Fores; Alexander J. Kugel; Cori S. Griesgraber; Mario A. Perez; Dana R. Reed |
| Two-part coating compositions are described comprising an aliphatic cyclic secondary amine and methods of coating surfaces of a (e.g. drinking water) pipeline. | ||||||
| 63 | Composition comprising cyclic secondary amine and methods of coating drinking water pipelines | US14001528 | 2012-02-21 | US09657193B2 | 2017-05-23 | Ryan B. Prince; Clinton L. Jones; Stuart E. Fores; Alexander J. Kugel; Cori S. Apel; Mario A. Perez; Dana R. Reed |
| Two-part coating compositions are described comprising an aliphatic cyclic secondary amine and methods of coating surfaces of a (e.g. drinking water) pipeline. | ||||||
| 64 | POLYCYCLOCARBONATE COMPOUNDS AND POLYMERS AND COMPOSITIONS FORMED THEREFROM | US15299610 | 2016-10-21 | US20170096579A1 | 2017-04-06 | Sebastien Gibanel; Benoit Prouvost |
| Polycyclocarbonate compounds and upgraded molecular weight polymers made from such compounds are provided. The polymers have particular utility in coating compositions, especially for use on food and beverage contact substrates that are formed into or will be formed into containers or container components. | ||||||
| 65 | FURAN-BASED POLYMERIC HYDROCARBON FUEL BARRIER STRUCTURES | US15105936 | 2014-12-18 | US20160311208A1 | 2016-10-27 | Fredrick Nederberg; Richard L. Bell; Jose Maria Torradas |
| Disclosed herein are multilayer structures and articles comprising the multilayer structures. The multilayer structure comprising a hydrocarbon fuel permeation barrier layer comprising furan-based polyester; a structural layer; and a tie layer interposed between the barrier layer and the structural layer, wherein the multilayer structure provides permeation barrier to the hydrocarbon fuel. | ||||||
| 66 | POLYESTER RESIN, RESIN COMPOSITION FOR CAN PAINT, PAINTED METAL PLATE FOR CAN, AND CAN | US14384228 | 2013-02-25 | US20150064378A1 | 2015-03-05 | Tetsuo Kawakusu |
| This invention provides a polyester resin that is capable of forming a coating film having extremely excellent curability, processability, retort resistance, content resistance, and dent resistance, and also provides a resin composition for a coating composition containing the polyester resin. The polyester resin obtained from a polycarboxylic acid component and a polyol component, wherein the polyester resin meets the conditions (i) to iii) described below: (i) among the polycarboxylic acid components constituting the polyester resin, the total copolymerization ratio of terephthalic acid component and 2,6-naphthalenedicarboxylic acid component is 80 mol % or more; (ii) among the polycarboxylic acid components constituting the polyester resin, the copolymerization ratio of 2,6-naphthalenedicarboxylic acid component is 2 to 80 mol %; and (iii) among the polyol components constituting the polyester resin, the total copolymerization ratio of ethylene glycol component and 1,2-propylene-glycol component is 50 mol % or more, wherein the copolymerization ratio of 1,2-propylene-glycol component is excessive relative to the copolymerization ratio of the ethylene glycol component. | ||||||
| 67 | COMPOSITION COMPRISING CYCLIC SECONDARY AMINE AND METHODS OF COATING DRINKING WATER PIPELINES | US14001528 | 2012-02-21 | US20140010956A1 | 2014-01-09 | Ryan B. Prince; Clinton L. Jones; Stuart E. Fores; Alexander J. Kugel; Cori S. Apel; Mario A. Perez; Dana R. Reed |
| Two-part coating compositions are described comprising an aliphatic cyclic secondary amine and methods of coating surfaces of a (e.g. drinking water) pipeline. | ||||||
| 68 | RADIATION CURABLE COATING COMPOSITIONS FOR METAL | US13976803 | 2011-12-23 | US20130280544A1 | 2013-10-24 | Gary Pierce Craun; Kenneth James Gardner; Patricia Miller |
| Various embodiments of radiation curable coating compositions are provided. In one embodiment, a radiation curable coating composition includes a (meth)acrylate functional compound and an adhesion promoting (meth)acrylate compound. The radiation curable coating composition can also include a (meth)acrylate functional compound, a poly(meth)acrylate and a reactive diluent. The (meth)acrylate functional compound can be made from the reaction of a multifunctional isocyanate, a polyol and a hydroxyl functional (meth)acrylate in the presence of a catalyst. | ||||||
| 69 | RADIATION CURABLE COATING COMPOSITIONS FOR METAL | US13976763 | 2011-12-23 | US20130273383A1 | 2013-10-17 | Gary Pierce Craun; Kenneth James Gardner; Patricia Miller |
| Various embodiments of radiation curable coating compositions are provided. In one embodiment, a radiation curable coating composition includes a (meth)acrylate functional compound and an adhesion promoting (meth)acrylate compound. The radiation curable coating composition can also include a (meth)acrylate functional compound, a poly(meth)acrylate and a reactive diluent. The (meth)acrylate functional compound can be made from the reaction of a multifunctional isocyanate, a polyol and a hydroxyl functional (meth)acrylate in the presence of a catalyst. | ||||||
| 70 | Cross-linked polyester protective coatings | US11220354 | 2005-09-06 | US20070054140A1 | 2007-03-08 | Peter Mayr; James Robinson; Fritz Altmann |
| The invention relates to protective coating systems derived from a functional polyester resin, a cross-linker and a phenol-formaldehyde resin. Also provided is a method of coating a metal substrate using the protective coating systems to produce a cross-linked protective coating. Further provided is a composite material prepared with the coating system and, in certain embodiments, useful in fabricating metal foodstuffs storage containers. The composite material may be particularly useful in fabricating foodstuffs storage containers and “easy-open” end closures wherein the cross-linked protective coating contacts the foodstuffs. | ||||||
| 71 | Carbamated polyols, and compositions and methods using the same | US10431710 | 2003-05-08 | US20040224109A1 | 2004-11-11 | Paul J. Lynch; Michael T. List; Ron D. Taylor; Kareem Kaleem; Youssef Moussa |
| The present invention is directed to coatings that provide improved retort and tropical decay resistance for use on metal food containers. The coatings generally comprise a carbamated polyol formed by the reaction between a polyol, an alkylene oxide and an alkyl carbamate. A crosslinker reactive with the carbamate functionality is used to react with the carbamate moiety. Methods for improving retort resistance and resistance to tropical decay are also disclosed, as are substrates coated with the present compositions. | ||||||
| 72 | Thermally setting substance mixture and use thereof | US10343848 | 2003-04-10 | US20030181539A1 | 2003-09-25 | Hubert Baumgart; Uwe Meisenburg; Karl-Heinz Joost |
| A heat-curable composition comprising (I) at least one constituent whose molecule comprises on average (A) at least one functional group containing at least one bond which may be activated by means of heat and/or actinic radiation, and/or (B) at least one reactive functional group which is able to undergo thermal crosslinking reactions with groups of its own kind and/or with complementary reactive functional groups, with the proviso that there are always groups (A) and (B) in the composition; said constituent excluding the polyurethane dispersion synthesized from aliphatic polyisocyanates, compounds containing isocyanate-reactive functional groups and containing bonds that may be activated with actinic radiation, low molecular mass aliphatic compounds containing isocyanate-reactive functional groups, compounds containing isocyanate-reactive functional groups and dispersing functional groups, neutralizing agents for the dispersing functional groups, blocking agents for isocyanate groups, and/or compounds containing blocked isocyanate groups, the blocked isocyanate groups being introduced into the polyurethane dispersion by the reaction of the blocking agents with isocyanato-containing polyurethane prepolymers; and (II) from 0.5 to 15% by weight, based on the solids of the heat-curable composition, of at least one CnullC-cleaving initiator. | ||||||
| 73 | Method of coating a packaging container using crosslinkable polyester-polyurethane | US10365064 | 2003-02-12 | US20030152778A1 | 2003-08-14 | Girish G. Parekh; Gregory M. Paulson; Ronald L. Goodwin |
| The present invention provides a method of coating a packaging container with a coating composition having crosslinkable polyester-polyurethane polymer with at least two carbamate sites, and a crosslinker. The method includes coating a generally planar substrate with the coating composition, curing and forming a container or a portion of a container. The present invention also provides a coating composition and coated substrates. | ||||||
| 74 | Process for the preparation of an N-alkyl or N-aryl carbamoyl derivative | US09815268 | 2001-03-23 | US20020028932A1 | 2002-03-07 | Jacobus A. Loontjens; Bartholomeus J.M. Plum |
| The invention relates to a process for the preparation of an N-alkyl or N-aryl carbamoyl derivative in which an amine is contacted with a carbonic acid derivative according to the general formula: 1 where fragments X in the form of XH are a lactam, oxime, imide or triazole. In particular the invention relates to the preparation of a blocked isocyanate according to a process in which no isocyanate is used. The invention also relates to the use of the N-alkyl or N-aryl carbamoyl derivative prepared according to the process according to the invention in a coating. | ||||||
| 75 | Method for improving physical characteristics of cured container coatings subjected to steam processing | US575197 | 1995-12-20 | US5665433A | 1997-09-09 | Youssef Moussa; Kareem K. Kaleem |
| A method for improving physical characteristics of cured container coatings subjected to steam processing is described herein. The method comprises applying a coating composition including a first component which is a carbamate functional compound and a second component which is a compound having a plurality of functional groups that are reactive with said carbamate group(s) on the carbamate functional compound. The coating composition is baked to form a cured film on the container. The container is filled and subjected to steam processing conditions suitable for food and beverage processing. | ||||||
| 76 | Controlling the rate of diamine curing agents in polyurethane cements | US722629 | 1985-04-12 | US4554299A | 1985-11-19 | Paul E. Liggett |
| A method for preparing a polyurethane which has good long term flexibility, solvent resistance and resistance to hydrolysis, said method comprising mixing three components just prior to curing said components comprising a prepolymer solution, a cement solution and a crosslinking solution, said crosslinking solution comprising a solvent, an aromatic diamine and the ketimine of an aliphatic diamine. | ||||||
| 77 | Fuel and hydrolysis resistant polyurethane | US588598 | 1984-03-12 | US4487913A | 1984-12-11 | Daniel A. Chung |
| A polyester polyurethane compound is formed by reacting trans-1,4-cyclohexanediisocyanate with a mixed polyester. The mixed polyester can be the copolymerization condensation product of an aliphatic dicarboxylic acid or an aromatic dicarboxylic acid, or a separate physical blend thereof reacted with a polyol. The polyurethane can also contain small amounts of non-extractable epoxies and carbodiimides. The urethane has very good hydrolytic stability in comparison with prior art polyurethane systems and also very good fuel resistance and anti-icing resistance. A preferred area of use is an aircraft fuel tanks and anti-icing components. | ||||||
| 78 | Sulfuric acid-resistant polyurethane composition and method of preparation | US665215 | 1976-03-09 | US4021414A | 1977-05-03 | Jeffrey W. Saracsan |
| A polyurethane composition, resistant to sulfuric acid, prepared by reacting 2,2'-diaminodisulfide with an isocyanate-terminated prepolymer, itself prepared by reacting, in the presence of a 2,6-dialkylated para cresol, at least one polymeric polyol with a diphenyl methane diisocyanate. | ||||||
| 79 | フランベースのポリマー炭化水素燃料バリア構造 | JP2016541262 | 2014-12-18 | JP2017501906A | 2017-01-19 | フレドリック・ネダーバーグ; リチャード・エル・ベル; ホセ・マリア・トラダス |
| 多層構造およびその多層構造を含む物品が、本明細書において開示される。その多層構造は、フランベースのポリエステルを含む炭化水素燃料透過バリア層;構造層;およびバリア層と構造層の間に置かれる結合層;を含み、炭化水素燃料に対する透過バリアを提供する。 | ||||||
| 80 | Metal base material for coating composition | JP2004526304 | 2003-08-01 | JP4648000B2 | 2011-03-09 | エム． オブライエン，ロバート; サード ジョージ ケー． バートリー，ザ; ジー． パレカー，ギリシュ; イー． フックス，ポール; エム． ポールソン，グレゴリー; イー． ラードン，ダニエル |
| The present invention provides novel packaging articles, e.g., food and beverage cans. Preferred cans typically comprise a body portion and an end portion, wherein at least one of the body and end portions are aluminum and are coated on at least one major surface with a coating composition of the present invention. Suitable coating compositions of the present invention comprise: one or more polyester resins, wherein at least one of the polyester resins has a glass transition temperature ("T g ") less than about 50°C, and wherein the polyester resin is formed by the reaction of one or more polyacid molecules and one or more polyol molecules; and a crosslinker. Preferred compositions are substantially free of mobile BPA and aromatic glycidyl ether compounds, e.g., BADGE, BFDGE and epoxy novalacs (e.g., NOGE) and more preferred compositions are also substantially free of bound BPA and aromatic glycidyl ether compounds. In more preferred embodiments (e.g., alcoholic beverage cans), the polyol molecules used to make the polyester resin are substantially free of NPG. The present invention also provides a method of making such cans. | ||||||
QQ群二维码
意见反馈
意见反馈