| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 21 | PHOTOALIGNMENT OF MATERIALS INCLUDING LIQUID CRYSTALS | US13786904 | 2013-03-06 | US20130333612A1 | 2013-12-19 | Timothy M. Swager; Jason R. Cox |
| Embodiments described herein relate to compositions, devices, and methods for the alignment of certain materials including liquid crystals. In some cases, a photoresponsive material include a moiety capable of undergoing a di-pi-methane rearrangement. Methods described herein may provide chemically and/or thermally stable alignment materials for use in a various technologies, including transistors, luminescent devices, and liquid crystal devices. | ||||||
| 22 | CARBOHYDRATE BINDERS AND MATERIALS MADE THEREWITH | US13696452 | 2011-05-07 | US20130047888A1 | 2013-02-28 | Gert R. Mueller; Charles Fitch Appley; Benedicte Pacorel; Carl A. Hampson |
| A binder comprising a polymeric binder comprising the products of a carbohydrate reactant and nucleophile is disclosed. The binder is useful for consolidating loosely assembled matter, such as fibers. Fibrous products comprising fibers in contact with a carbohydrate reactant and a nucleophile are also disclosed. The binder composition may be cured to yield a fibrous product comprising fibers bound by a cross-linked polymer. Further disclosed are methods for binding fibers with the carbohydrate reactant and polyamine based binder. | ||||||
| 23 | Improved poly(aryletherketone)s and process for making them | US12672244 | 2008-08-08 | US20110224399A1 | 2011-09-15 | Chantal Louis; Satchit Srinivasan; William Gandy |
| Improved poly(aryletherketone)s with superior melt stability, lower gel content and lower color and a new process for their manufacture. | ||||||
| 24 | Bisphenol aryl fluoride AB2 monomer and the hyperbranched polymer therefrom | US10083968 | 2002-02-27 | US06512124B1 | 2003-01-28 | Jong-Beom Baek; Loon-Seng Tan |
| A self-polymerizable AB2 monomer of the formula The resulting AB2 monomer can be polymerized to afford high molecular, low viscosity hyperbranched ether-ketone-imide polymer having repeating units with hydroxyl endgroups. | ||||||
| 25 | Liquid oligomers containing unsaturation | US933811 | 1997-09-19 | US5945489A | 1999-08-31 | Thomas M. Moy; Laurence Dammann; Roman Loza |
| The liquid oligomeric compositions of this invention are made by the Michael addition reaction of acetoacetate functional donor compounds with multifunctional acrylate receptor compounds where the equivalent ratios of multifunctional acrylate to acetoacetate vary from .gtoreq.1:1 to .gtoreq.13.2:1 depending on the functionality of both multifunctional acrylate and acetoacetate. Unuseable gelled or solid oligomer products occur below the claimed ranges. The liquid oligomers of this invention are further crosslinked to make coatings, laminates and adhesives. | ||||||
| 26 | Phenolic-resin-modified natural resin acid esters, a process for their preparation and their use as binder resins in printing inks | US380634 | 1995-01-30 | US5597884A | 1997-01-28 | Albert Bender |
| Phenolic-resin-modified natural resin acid esters, a process for their preparation and their use as binder resins printing inks.Phenolic-resin-modified natural resin acid esters obtained by reaction ofA) natural resins and natural resin acids,B) mononuclear and polynuclear alkylolizable phenols,C) aldehydes and aldehydes acetals,D) aliphatic, cycloaliphatic and araliphatic polyols,E) calcium compounds and/or zinc compounds andF) optionally ethylenically unsaturated hydrocarbon resins,at a temperature of 100.degree. to 250.degree. C., and subsequent removal of the water by azeotropic distillation with an entraining agent at 200.degree. to 300.degree. C. | ||||||
| 27 | Reaction product of olefinically unsaturated compounds with compounds containing active hydrogen, processes for their preparation and 2-component lacquers based thereon | US371517 | 1989-06-26 | US5084536A | 1992-01-28 | Gerhard Brindopke; Gerd Walz; Karl Waldmann; Manfred Schon; Hans-Jerg Kleiner |
| A 3-component lacquer composed of A) compounds containing at least two R.sup.1 R.sup.2 C.dbd.CR.sup.3 --X groups (I) wherein R.sup.1 denotes hydrogen or a hydrocarbon radical having 1 to 10 carbon atoms, R.sup.2 and R.sup.3 are individually hydrogen, a hydrocarbon radical having 1 to 10 carbon atoms, an ester group containing the radical R.sup.4 of a monohydric alcohol having up to 12 carbon atoms, --CN, --NO.sub.2 or a --CO--NHR.sup.1 or --CO--R.sup.1 group, X is --CO-- which is attached to a further R.sup.1 R.sup.2 C.dbd.CR.sup.3 -- group either directly or via the radical of a polyhydric alcohol or of an amine and B) compounds containing:(a) at least two active H atoms or(b) at least two groups having active H atoms of the type --AH (II) or(c) at least one active H atom and at least one group of the type (II)and A is --CH-- or --NH-- or --S-- and optionally with customary additives and C) at least one catalyst selected from the group consisting of diazabicyclooctane (DABCO), fluorides of quaternary ammonium compounds on their own or as a mixture with alkyl silicates, amidines, tertiary phosphanes of the formula P(CH.sub.2 --Y).sub.3 in which the Ys are identical or different and are --OH, --CH.sub.2 CN or --N(Z).sub.2 in which Z is an alkyl having 1 to 5 carbon atoms, tertiary phosphanes of the formula P(R.sup.4,R.sup.5,R.sup.6) in which R.sup.4, R.sup.5 and R.sup.6 are alkyl of 1 to 12 carbon atoms or a phenyl which is unsubstituted or substituted by at least one alkyl, alkoxy or dialkylamino, each of which has 1 to 4 carbon atoms in the alkyl, and R.sup.4, R.sup.5 and R.sup.6 are identical or different, but at least one of them is phenyl, and aminophosphoranes of the formula (R.sup.7,R.sup.8,R.sup.9) P.dbd.N--C (R.sup.10, R.sup.11,R.sup.12) in which R.sup.7, R.sup.8 and R.sup.9 are identical or different and denote an alkyl having 1 to 12 carbon atoms or a alkoxy or dialkylamino group, each of which has 1 to 4 carbon atoms in the alkyl, and R.sup.10, R.sup.11 and R.sup.12 are identical or different and each represents an alkyl having 1 to 5 carbon atoms or a phenyl. | ||||||
| 28 | Resorcinol-modified phenolic resin binder for reinforced plastics | US577804 | 1990-09-04 | US5075413A | 1991-12-24 | Theodore H. Dailey, Jr. |
| A fire resistant resin for use as a binder in reinforced plastics and a resultant reinforced plastic includes the reaction product of (a) at least one resorcinol component selected from the group consisting of resorcinol and resorcinol formaldehyde novolak resin, and (b) a phenolic resole resin. The reaction may be achieved in the presence of an alkaline catalyst.A method of making a fire resistant resin binder for reinforced plastics and the method of making such reinforced plastics including, (a) at least one resorcinol component selected from the group consisting of resorcinol and resorcinol formaldehyde novolak resin, and (b) a phenolic resole resin. The reaction may be achieved in the presence of an alkaline catalyst. | ||||||
| 29 | Marine paint composition comprising quinone/polyamine polymer | US280141 | 1988-12-05 | US4981946A | 1991-01-01 | Semih Erhan |
| A marine paint composition comprising a polymer of the formula: ##STR1## wherein R is alkyl, monocyclic cycloalkyl, monocyclic heterocyclic, aromatic, siloxy, silyl and the alkyl, alkoxy, carboxyl and amino substituted derivatives thereof, and n is about 70 to 700, and a suitable carrier. | ||||||
| 30 | Reaction product of olefinically unsaturated compounds with compounds containing active hydrogen, processes for their preparation and 2-component lacquers based thereon HOE 85/F O36J | US874688 | 1986-06-16 | US4871822A | 1989-10-03 | Gerhard Brindopke; Gerd Walz; Karl Waldmann; Manfred Schon; Hans-Jerg Kleiner |
| A reaction product of (A) compounds containing at least two R.sup.1 R.sup.2; C.dbd.CR.sup.3 --X groups (I) with (B) compounds which contain(a) at least two active H atoms or(b) at least two groups containing active H atoms of the type --AH-- (II) or(c) at least one active H atom and at least one group of the type (III),or which form the corresponding amount of this group (II), in which, the formula (I),X denotes --CO-- which is attached to a further R.sup.1 R.sup.2 C.dbd.CR.sup.3 group either directly or via the radical of a polyhydric alcohol or of an amine,R.sup.1 denotes hydrogen or a hydrocarbon radical having 1 to 10, preferably 1 to 4, carbon atoms, such as alkyl, phenyl, benzyl or naphthyl,R.sup.2 denotes hydrogen, a hydrocarbon radical having 1 to 10, preferably 1 to 4, carbon atoms, such as alkyl, phenyl, benzyl or naphthyl, an ester group containing the radical R.sup.4 of a monohydric alcohol having up to 12 carbon atoms, --CN, --NO.sub.2 or a CO--NHR.sup.1 or CO--R.sup.1 group, andR.sup.3 has the same meaning as R.sup.2 and is identical with or different from the latter, and in formula (II), --AH-- denotes one of the grouping --CH--, --NH-- and --SH, subject to the proviso that reaction products of (A) polyacrylates containing at least two free acrylic acid groups, reaction products of polyisocyanates with acrylic acid esters containing OH groups or reaction products of epoxy resins, with acrylic acid, with (B) diketene or acetoacetic acid esters of hydroxyethyl acrylate or methacrylate are excluded. In the reaction product, component (A) is a Michael acceptor and component (B) is a Michael donor. The product of the invention has the advantage that it is prepared from components which contain no toxic constituents and can therefore be used without special precautionary measures. | ||||||
| 31 | Solvent strippable photosensitive compositions and method of production therefor | US3458312D | 1966-09-19 | US3458312A | 1969-07-29 | SRINIVASAN RANGASWAMY |
| 32 | Resin made from tannin, sulfuric acid, acetone, and potassium cyanide | US2361648 | 1948-04-27 | US2590760A | 1952-03-25 | DA VEIGA VINICIO |
| 33 | Reaction products of acrylonitrile with macromolecular ketones | US52348344 | 1944-02-22 | US2396963A | 1946-03-19 | WALTER MORTENSON CARL |
| 34 | Manufacture of hydroxy-keto compounds having a cyclopentanopolyhydrophenanthrene nucleus | US33301240 | 1940-05-01 | US2363548A | 1944-11-28 | RUPERT OPPENAUER |
| 35 | Pectose resins and method of making same | US61463532 | 1932-05-31 | US1941351A | 1933-12-26 | ADOLF HAWERLANDER |
| 36 | Acetals of cyclic ketones with polyhydric alcohols and process of preparing the same | US59667232 | 1932-03-03 | US1902866A | 1933-03-28 | GEORG KRANZLEIN; EWALD DICKHAUSER; ARTHUR VOSS |
| 37 | LIQUID HIGH SOLIDS BINDER COMPOSITION | US15822102 | 2017-11-24 | US20180142099A1 | 2018-05-24 | Gert MUELLER |
| The invention described herein pertains to formaldehyde free, thermosetting liquid high solids binder compositions having rapid cure times on thermal curing and slow cure times at ambient temperatures so that the uncured binder compositions and products which comprise the uncured binder compositions have improved shelf lives. | ||||||
| 38 | RESIST UNDERLAYER FILM FORMING COMPOSITION FOR LITHOGRAPHY CONTAINING HYDROLYZABLE SILANE HAVING HALOGEN-CONTAINING CARBOXYLIC ACID AMIDE GROUP | US15533237 | 2015-12-04 | US20170322491A1 | 2017-11-09 | Wataru SHIBAYAMA; Kenji TAKASE; Rikimaru SAKAMOTO |
| A resist underlayer film forming composition for lithography that can be used as a hard mask. The composition can improve pattern resolution due to having a trihalogenoacetamide skeleton. A resist underlayer film forming composition for lithography comprising a hydrolyzable silane, a hydrolysis product thereof, a hydrolysis condensate thereof, or a combination thereof as a silane, wherein the hydrolyzable silane comprises a silane having a halogen-containing carboxylic acid amide group. | ||||||
| 39 | CARBOHYDRATE BINDERS AND MATERIALS MADE THEREWITH | US15276283 | 2016-09-26 | US20170015694A1 | 2017-01-19 | Gert R. MUELLER; Charles Fitch APPLEY; Benedicte Pacorel; Carl A. HAMPSON |
| A binder comprising a polymeric binder comprising the products of a carbohydrate reactant and nucleophile is disclosed. The binder is useful for consolidating loosely assembled matter, such as fibers. Fibrous products comprising fibers in contact with a carbohydrate reactant and a nucleophile are also disclosed. The binder composition may be cured to yield a fibrous product comprising fibers bound by a cross-linked polymer. Further disclosed are methods for binding fibers with the carbohydrate reactant and polyamine based binder. | ||||||
| 40 | Carbohydrate binders and materials made therewith | US13696452 | 2011-05-07 | US09493603B2 | 2016-11-15 | Gert R. Mueller; Charles Fitch Appley; Benedicte Pacorel; Carl A. Hampson |
| A binder comprising a polymeric binder comprising the products of a carbohydrate reactant and nucleophile is disclosed. The binder is useful for consolidating loosely assembled matter, such as fibers. Fibrous products comprising fibers in contact with a carbohydrate reactant and a nucleophile are also disclosed. The binder composition may be cured to yield a fibrous product comprising fibers bound by a cross-linked polymer. Further disclosed are methods for binding fibers with the carbohydrate reactant and polyamine based binder. | ||||||
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