| 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 | 涂料组合物和由其制备的可低温固化涂层及其用途 | CN201480052055.5 | 2014-08-07 | CN105555821A | 2016-05-04 | P·霍夫曼; R·克洛普施; M·格罗尼沃尔特; E·维斯林; A·弗洛雷斯-菲圭罗阿; K·米歇尔 |
| 本发明涉及非水性涂料组合物，其包含：至少一种具有至少两个氨基的化合物(A)，和至少一种具有至少两个亚烷基-1,3-二氧戊环-2-酮基团的低聚和/或聚合化合物(B)，其中化合物(B)可使用以下单体得到：至少一种式(I)的单体(B1)，其中R1、R2相互独立地为氢、C1-C6烷基、C1-C4烷氧基-C1-C4烷基、C5-C6环烷基、苯基或苯基-C1-C4烷基；R3为氢、C1-C6烷基、C1-C4烷氧基-C1-C4烷基、C5-C6环烷基、苯基或苯基-C1-C4烷基、R3更特别为氢；R4为氢、C1-C4烷基、CH2COOR8、苯基或苯基-C1-C4烷基；R5、R6相互独立地为氢或C1-C4烷基，或者R5或R6基团中的一个可以为COOR8或CH2COOR8；A为化学键或C1-C4亚烷基，A更特别是C1-C4亚烷基；X为O或NR7；Z为化学键、PO2、SO2或C＝O，Z更特别是C＝O；Y为化学键、CH2或CHCH3；R7如果存在的话为C1-C6烷基；且R8如果存在的话为氢或C1-C6烷基；和各自不同于单体(B1)的至少两种不同共聚单体(B2)和(B3)。本发明进一步提供由这些涂料组合物制备的涂层及其用途。 | ||||||
| 2 | 木质纤维材料粘合法的改进 | CN85102125 | 1985-04-01 | CN85102125A | 1987-01-31 | 查普曼; 詹金 |
| 这一发明是关于纤维板，碎料板和胶合板等复制木制品生产过程中，以可热固的树脂粘合如木头等的木质纤维素材料的一种方法。根据这种方法，制作过程中在木纤维、碎料或薄木片中加进一种产生放热反应的化学物质。在对纤维、碎料或薄木片加压时，那种产生放热反应的化学物质在生产的纤维板，碎料板或胶合板内参与放热反应，提供热。这些热使可热固树脂较其它情况下更快凝固。这一方法的产品也请求专利权。 | ||||||
| 3 | 交联组合物 | CN200480008686.3 | 2004-02-26 | CN100503674C | 2009-06-24 | L-T·W·林; W·雅各布斯三世 |
| 本发明涉及一种交联组合物，包含具有式I结构的化合物：A′-NRA-RD，其中，A′是源自下列基团的部分：线型或环脲、氰尿酸、取代的氰尿酸、线型或环酰胺、甘脲、乙内酰脲、线型或环氨基甲酸酯，以及它们的混合物，或包含式II结构的部分：其中，RA是RD、氢、1-20个碳原子的烷基，或与A’一起形成环化合物；RD是-CHRCORB，其中RB是氢、有1-24个碳原子的烷基、芳基、芳烷基或烷芳基，RC是有1-24个碳原子的烷基、卤化烷基、芳基、芳烷基、卤化芳烷基、烷氧基烷基或烷芳基；A是源自下列基团的部分：线型或环脲、氰尿酸、取代的氰尿酸、线型或环酰胺、甘脲、乙内酰脲、线型或环氨基甲酸酯，以及它们的混合物；B是有n个醛基的多(烷基醛)的残基；n是2-8的整数；RA是RD、氢、1-20个碳原子的烷基，或与A一起形成环状化合物；其中RD是CHRCORB，其中RB是氢、有1-24个碳原子的烷基、芳基、芳烷基或烷芳基，RC是有1-24个碳原子的烷基、卤化烷基、芳基、芳烷基、卤化芳烷基、烷氧基烷基或烷芳基；各基团上的烷基或芳基还可以在其结构中有杂原子。本发明还涉及制备交联组合物的方法，包括使含氨基的氨基化合物；单(烷基醛)和/或多(烷基醛)；和醇反应；所述氨基化合物选自下列：线型或环脲、氰尿酸、取代的氰尿酸、线型或环酰胺、甘脲、乙内酰脲、线型或环氨基甲酸酯，以及它们的混合物。 | ||||||
| 4 | 交联组合物 | CN200480008686.3 | 2004-02-26 | CN1768087A | 2006-05-03 | L-T·W·林; W·雅各布斯三世 |
| 本发明涉及一种交联组合物，包含具有式I结构的化合物：A′－NRA－RD，其中，A′是源自下列基团的部分：线型或环脲、氰尿酸、取代的氰尿酸、线型或环酰胺、甘脲、乙内酰脲、线型或环氨基甲酸酯，以及它们的混合物，或包含式II结构的部分：其中，RA是RD、氢、1－20个碳原子的烷基，或与A′一起形成环化合物；RD是－CHRCORB，其中RB是氢、有1－24个碳原子的烷基、芳基、芳烷基或烷芳基，RC是有1－24个碳原子的烷基、卤化烷基、芳基、芳烷基、卤化芳烷基、烷氧基烷基或烷芳基；A是源自下列基团的部分：线型或环脲、氰尿酸、取代的氰尿酸、线型或环酰胺、甘脲、乙内酰脲、线型或环氨基甲酸酯，以及它们的混合物；B是有n个醛基的多(烷基醛)的残基；n是2－8的整数；RA是RD、氢、1－20个碳原子的烷基，或与A一起形成环状化合物；其中RD是CHRCORB，其中RB是氢、有1－24个碳原子的烷基、芳基、芳烷基或烷芳基，RC是有1－24个碳原子的烷基、卤化烷基、芳基、芳烷基、卤化芳烷基、烷氧基烷基或烷芳基；各基团上的烷基或芳基还可以在其结构中有杂原子。本发明还涉及制备交联组合物的方法，包括使含氨基的氨基化合物；单(烷基醛)和/或多(烷基醛)；和醇反应；所述氨基化合物选自下列：线型或环脲、氰尿酸、取代的氰尿酸、线型或环酰胺、甘脲、乙内酰脲、线型或环氨基甲酸酯，以及它们的混合物。 | ||||||
| 5 | 직물처리 조성물 | KR1019810003562 | 1981-09-23 | KR1019830007949A | 1983-11-09 | 브루노키슬링 |
| 내용없음 | ||||||
| 6 | N-methylol derivative of polycondensate, and preparation and use thereof | JP2576995 | 1995-01-23 | JPH07238167A | 1995-09-12 | UDOOBINFURIITO HENDORIKUSU; RARUFU HAINEN |
| PURPOSE: To obtain an N-methylol deriv. of a polycondensate which is useful as an agent for improving the wet fastness properties of dyeings and prints by reacting a specific basic urea compd., a polyamine, and a bifunctional alkylating agent. CONSTITUTION: A basic urea compd. of formula I (wherein X 1 is 2-4C alkylene; R 1 and R 2 are each H, 1-4C alkyl or the like; R 3 and R 4 are each H, 1-4C alkyl, 2-4C hydroxyalkyl or the like; and R 5 is H, 1-4C alkyl, 2-4C hydroxyalkyl or a group of formula II or III), a polyamine of formula IV (wherein X 2 is 2-6C alkylene or the like; R 10 is H or 1-4C alkyl; and R 6 to R 9 are each H, 1-4C alkyl, 2-4C aminoalkyl or the like), and a bifunctional alkylating agent are reacted in a molar ratio of (0.5-2.5):1: (1.0-3.2) in water or a polar org. solvent. The resultant product is reacted with formaldehyde (or a formaldehyde-releasing compd.) in an amt. of 0.5-1.2 mol, based on 1 mol of urea group: -N(R 2)-CO-NH (R 1)- of the product, at 40-130°C at a pH of 8-11. COPYRIGHT: (C)1995,JPO | ||||||
| 7 | JPS6241605B2 - | JP16674782 | 1982-09-27 | JPS6241605B2 | 1987-09-03 | TEODOORU AA BIRUGE; YURUKU BIDOMAA; TEODOORU MEIYAA; URURITSUHI ZURUSAA |
| 8 | Dyeing, printing and fluorescent brightening method of spun fiber | JP27498784 | 1984-12-28 | JPS60155788A | 1985-08-15 | YURUKU HERAA; BURUNO KITSUSHIYURINKU; TEIBORU ROBINSON; SARUBATOORE BARENTEI; PIITAA JIINZU; JIEIMUZU MAACHIN TEIRAA |
| 9 | Treatment of dispersion liquid of capsule | JP10937879 | 1979-08-27 | JPS5633030A | 1981-04-03 | HORIIKE TETSUROU; OKIMOTO SATOYUKI; SHIOZAKI TOMOHARU |
| PURPOSE:To remove the residual formaldehyde without spoiling the capacity of membrane, by adjusting the dispersion liquid of microcapsule having the wall membrane of aldehyde polycondensation resin in alkaline condition and then, heating and stirring after adding the reaction catalyst, such as metal hydroxide. CONSTITUTION:Residual formaldehyde in the dispersion liquid of microcapsule having the wall membrane of aldehyde polycondensation resin whicn is formed by the curing reaction of acid catalyst by using formaldehyde as one component, is heated and stirred in alkaline solution and then, is removed after adding the reaction catalyst, such as metal hydroxides or phosphates. By this method, formaldehyde can be effectively removed by the chemical denaturation treatment without spoiling a superior capacity of the capsule wall membrane. | ||||||
| 10 | Polyaddition product of ammonia and epoxy compound and its denaturing method | JP4576780 | 1980-04-09 | JPS55149318A | 1980-11-20 | FURITSUTSU ERUTOMAN KEMUPUTAA; EBERUHARUTO SHIYUTSUPU; HANSUUUUBUE SHIENKU; EERIHI GURUBINSU |
| 11 | JPS5427312B1 - | JP4607071 | 1971-06-26 | JPS5427312B1 | 1979-09-08 | |
| 12 | Method of making aminoplast dispersion and its use | JP2937876 | 1976-03-19 | JPS51117793A | 1976-10-16 | KUUNO BAAGUNERU; YURUGEN ITSUKU; GERUHARUTO BAREE |
| 13 | JPS50109295A - | JP1226675 | 1975-01-29 | JPS50109295A | 1975-08-28 | |
| 14 | CROSSLINKING COMPOSITION | EP04715054.5 | 2004-02-26 | EP1608691B8 | 2018-06-13 | LIN, Lon-Tang, Wilson; JACOBS, William, III |
| This invention relates to a crosslinking composition comprising a compound having the structure of Formula I: A'-NRA-RD where A' is a moiety derived from the group consisting of linear or cyclic ureas, cyanuric acid, substituted cyanuric acids, linear or cyclic amides, glycolurils, hydantoins, linear or cyclic carbamates and mixtures thereof, or a moiety comprising the structure: where RA is RD, hydrogen, an alkyl of 1 to 20 carbon atoms, or taken together with A' forms a cyclic compound; RD is -CHRC ORB, wherein RB is hydrogen, alkyl, aryl, aralkyl or an alkaryl having from 1 to about 24 carbon atoms and RC is an alkyl, halogenated alkyl, aryl, aralkyl, halogenated aralkyl, alkoxyalkyl or an alkaryl having from 1 to about 24 carbon atoms; A is a moiety derived from the group consisting of linear or cyclic ureas, cyanuric acid, substituted cyanuric acids, linear or cyclic amides, glycolurils, hydantoins, linear or cyclic carbamates and mixtures thereof; B is a residue of a poly(alkylaldehyde) with n aldehyde groups; n is an integer of 2 to about 8; Ra is Rd, hydrogen, an alkyl of 1 to about 20 carbon atoms, or taken together with A forms a cyclic compound; where Rd is CHRcORb or where Rb is hydrogen, alkyl, aryl, aralkyl or an alkaryl having from 1 to about 24 carbon atoms and Rc is an alkyl, halogenated alkyl, aryl, aralkyl, halogenated aralkyl, alkoxyalkyl or an alkaryl having from 1 to about 24 carbon atoms; and where the alkyl or aryl groups in each radical may optionally have heteroatoms in their structure. This invention also relates to a process for producing the crosslinking composition by reacting an amino compound containing amino groups; a mono(alkylaldehyde) and/or a poly(alkylaldehyde), and an alcohol; where said amino compound is selected from the group consisting of: linear or cyclic ureas, cyanuric acid, substituted cyanuric acids, linear or cyclic amides, glycolurils, hydantoins, linear or cyclic carbamates and mixtures thereof. | ||||||
| 15 | High molecular weight amine containing antiozonants | EP93118562.3 | 1993-11-18 | EP0654489A1 | 1995-05-24 | Sturm, Budd Harvey; Kuczkowski, Joseph Andrew; Sandstrom, Paul Harry; Balogh, George Frank |
The present invention relates to a composition which exhibits antiozonant activity in diene containing rubbers comprising the reaction product of a multi-step process comprising:
|
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| 16 | Dyeing and printing fibres | EP84810651.4 | 1984-12-20 | EP0151370B1 | 1990-03-14 | Heller, Jürg; Kissling, Bruno; Robinson, Tibor; Valenti, Salvatore; Ginns, Peter; Taylor, James Martin |
| 17 | Process for bonding water penetrable cellulosic particles | EP87600007.6 | 1987-05-29 | EP0252867A1 | 1988-01-13 | Markessini, Vergopoulou Efthalia |
A substitute for amino and phenolic resins is disclosed. It is used in the polycondensation of such resins based on formaldehyde for bonding water penetrable cellulosic particles. The substitute comprises an aqueous solution of
This substitute also reduces the free formaldehyde of the resulting board without impairing the other properties thereof. |
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| 18 | Baustoffe,enthaltend ein Polykondensationsprodukt | EP82108240.1 | 1982-09-08 | EP0077904B1 | 1987-08-05 | Bürge, Theodor; Widmer, Jürg; Meyer, Theodor; Sulser, Ulrich |
| 19 | Umsetzungsprodukte und Kondensationsprodukte auf Basis substituierter Propylenharnstoffe, deren Herstellung und Verwendung | EP86109185.8 | 1986-07-04 | EP0210471A2 | 1987-02-04 | Goeckel, Ulrich, Dr.; Petersen, Harro, Dr.; Osterloh, Rolf, Dr.; Schupp, Eberhard, Dr.; Loch, Werner, Dr.; Schwerzel, Thomas, Dr. |
Die Erfindung betrifft Kodensationsprodukte auf Basis substituierter Harnstoffe, deren Umsetzugspro- dukte mit Di-und/oder Polyisocyanaten, Derivaten von Di-und/oder Polycarbonsäuren oder p-substituierten Phenolen und/oder deren Methylolderivaten, deren Herstellung und Verwendung. Diese Kondensationsprodukte enthalten jeweils mindestens zwei cyclische Harnstoffeinheiten und lassen sich entweder durch Umsetzung primärer Di-oder Polyamine mit Harnstoffen und anschließende Reaktion mit überwiegend C-H-aciden Aldehyden oder durch Umsetzung primärer Amine mit lsocyanaten und anschließende Reaktion mit überwiegend C-H-aciden Aldehyden in Gegenwart saurer Katalysatoren herstellen. Diese Kondensationsprodukte und deren Umsetzungsprodukte eignen sich zur Herstellung hitzehärtbarer Überzugsmittel sowie zur Herstellung von Bindemitteln für die kathodische Elektrotauchlackierung. |
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| 20 | Hemiacetals of adducts of acrolein and isocyanuric acid and polymer compositions thereof | EP81305945.8 | 1981-12-18 | EP0055091B1 | 1985-07-31 | Cohen, Saul Mark; LeBlanc, John Roger |
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