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121. 发明申请

US20100191001A1 PROCESS FOR CONTROLLED HYDROLYSIS AND CONDENSATION OF EPOXY-FUNCTIONAL ORGANOSILANES AND THE COCONDENSATION THEREOF WITH FURTHER ORGANOFUNCTIONAL ALKOXYSILANES 有权
标题翻译：环氧官能有机物的控制水解和缩合方法及其与有机官能烷氧基化合物的共聚
公开(公告)号：US20100191001A1
公开(公告)日：2010-07-29
申请号：US12673390
申请日：2008-06-17
申请人： Christian Wassmer , Burkhard Standke , Irene Lippert , Peter Jenkner
发明人： Christian Wassmer , Burkhard Standke , Irene Lippert , Peter Jenkner
IPC分类号： C07D303/02 , C07F7/02
CPC分类号： C08G77/08 , C08G77/14
摘要： The present invention relates to a process for performing a controlled hydrolysis and condensation of an epoxy-functional silane of the general formula I R1-SiR′m(OR)3-m (I) in which R1 is a (III) or (IV) group and R, R′ and R″ groups are the same or different and are each hydrogen (H) or a linear, branched or cyclic, optionally substituted alkyl group having from 1 to 6 carbon atoms, A and A′ groups are the same or different and are each a bivalent alkyl group having from 1 to 10 carbon atoms, R2 groups are the same or different and R2 is a linear, branched or cyclic, optionally substituted alkyl group having from 1 to 20 carbon atoms, and m is 0 or 1, and optionally of at least one further organofunctional silane of the general formula II R2-SiR′n(OR)3-n (II) in which R2 is an organofunctional group as already defined above, R′ is methyl, R groups are each independently hydrogen or a linear, branched or cyclic alkyl group having from 1 to 6 carbon atoms and n is 0 or 1, where from 0.001 to ≦5 mol of water is used per mole of alkoxy function of the silanes used, no further hydrolysis or condensation catalyst is used apart from boric acid as the hydrolysis catalyst and condensation component, and the condensates formed in the reaction are based on Si—O—B— and/or Si—O—Si bonds.
摘要翻译：本发明涉及一种通式I R 1 -Si R'm（OR）3-m（I）的环氧官能硅烷进行受控水解和缩合的方法，其中R 1是（III）或（IV ）基团，R，R'和R“基团相同或不同，各自为氢（H）或具有1至6个碳原子的直链，支链或环状，任选取代的烷基，A和A'基团为相同或不同，各自为具有1至10个碳原子的二价烷基，R 2基团相同或不同，并且R 2为具有1至20个碳原子的直链，支链或环状的任选取代的烷基，m为 0或1，以及任选地至少一种另外的通式II的有机官能硅烷R2-SiR'n（OR）3-n（II），其中R2是如上定义的有机官能团，R'是甲基，R 基团各自独立地为氢或具有1至6个碳原子且n为0或1，w的直链，支链或环状烷基这里为0.001至＆lt; nlE;每摩尔使用的硅烷的烷氧基官能度使用5摩尔的水，除了作为水解催化剂和缩合组分的硼酸之外不再使用进一步的水解或缩合催化剂，反应中形成的缩合物基于Si-O-B和/或Si-O-Si键。

122. 发明申请

US20090069464A1 LIQUID VISCOUS PRODUCT BASED ON AN ORGANOFUNCTIONAL SILANE SYSTEM FOR PRODUCING WEATHERING-STABILE PROTECTIVE COATINGS FOR PREVENTING SURFACE SOILING 有权
标题翻译：基于用于生产用于防止表面土壤的耐候性保护涂料的有机硅烷系统的液体粘稠产品
公开(公告)号：US20090069464A1
公开(公告)日：2009-03-12
申请号：US11718442
申请日：2005-09-07
申请人： Burkhard Standke
发明人： Burkhard Standke
IPC分类号： C08L1/02 , C08L83/08 , C08K5/05 , C08K5/3415 , C08K5/3432 , B05D1/28 , B05D1/02
CPC分类号： C09D183/08 , C04B41/009 , C04B41/4961 , C04B2111/25 , C09D4/00 , C04B14/06 , C04B28/02 , C08G77/22
摘要： The present invention relates to a composition comprising an organofunctional silane system, in which fluorinated alkyl groups of the general formula F3C(CF2)r(CH2)s— (Ib) are attached to some of the silicon atoms, and a thickener, to a process for preparing such a composition, and to the use of the composition for preventing surface soiling.
摘要翻译：本发明涉及包含有机官能硅烷体系的组合物，其中通式为F3C（CF2）r（CH2）s-（Ib）的氟化烷基与一些硅原子连接，并且增稠剂与制备这种组合物的方法，以及该组合物用于防止表面污染的用途。

123. 发明授权

US07423186B2 Process for preparing alkoxy-pure alkaline earth alkoxides 失效
标题翻译：制备烷氧基 - 纯碱土金属醇盐的方法
公开(公告)号：US07423186B2
公开(公告)日：2008-09-09
申请号：US11010831
申请日：2004-12-13
申请人： Burkhard Standke , Hartwig Rauleder
发明人： Burkhard Standke , Hartwig Rauleder
IPC分类号： C07C41/14
CPC分类号： C07C29/705 , C07C31/28
摘要： The present invention provides a process for preparing a metal-free alkaline earth methanolate by alcoholysis of an alkaline earth ethanolate with methanol.
摘要翻译：本发明提供了一种通过碱土金属醇化物与甲醇的醇解制备无金属碱土金属甲醇的方法。

124. 发明授权

US06767982B2 Continuous manufacturing process for organoalkoxysiloxanes 有权
标题翻译：有机烷氧基硅氧烷的连续制造工艺
公开(公告)号：US06767982B2
公开(公告)日：2004-07-27
申请号：US09987267
申请日：2001-11-14
申请人： Burkhard Standke , Michael Horn
发明人： Burkhard Standke , Michael Horn
IPC分类号： C08G7706
CPC分类号： C08G77/18 , C07F7/0872 , C08G77/06 , C09D4/00 , C09D183/04 , C08G77/04
摘要： A mixture of organoalkoxysiloxanes of formula I: wherein R and R″ are identical or different and are methyl, ethyl, vinyl, n-propyl, i-propyl, &ggr;-chloropropyl, n-butyl, i-butyl, n-pentyl, i-pentyl, n-hexyl, i-hexyl, n-heptyl, i-heptyl, n-octyl, i-octyl, hexadecyl, octadecyl or alkoxy, R′ represents methyl or ethyl, n and m are identical or different and each is 0 or an integer ranging from 1 to 20, on the condition that (n+m)≧2, is prepared by: reacting in a first stage the constituents of (i) an organotrichlorosilane or a mixture of organotrichlorosilanes or a mixture of at least one organotrichlorosilane and tetrachlorosilane, (ii) water and (iii) alcohol, combined in a molar ratio (i):(ii):(iii) of 1:(0.59 to 0.95):(0.5 to 100), at a temperature of 0 to 150° C., which produces hydrogen chloride as a product which is removed from the system and the crude organoalkoxysiloxane product is transferred proportionately to the reaction distillation column of a subsequent second stage after an average dwell time of 0.5 to 180 minutes; and conducting reaction and distillation in the reaction distillation column in a second stage in which volatile constituents are withdrawn from the top of the column and the organoalkoxysiloxane product is withdrawn as a bottom product, wherein the reaction-distillation column is operated at a bottom temperature of 50 to 200° C.
摘要翻译：式I的有机烷氧基硅氧烷的混合物：其中R和R“相同或不同，是甲基，乙基，乙烯基，正丙基，异丙基，γ-氯丙基，正丁基，异丁基，正戊基，正戊基，正己基，异己基，正庚基，异庚基，正辛基，异辛基，十六烷基，十八烷基或烷氧基，R'表示甲基或乙基，n和m相同或不同，在（n + m）> = 2的条件下，为0或1〜20的整数，通过以下步骤制备：在第一阶段中使（i）有机三氯硅烷或有机三氯硅烷的混合物的组分或至少一种有机三氯硅烷和四氯硅烷，（ii）以1：（0.59至0.95）：（0.5至100）的摩尔比（i）：（ii）：（iii）组合的水和（iii）醇，温度为0至150℃，其产生作为从系统中除去的产物的氯化氢，粗有机烷氧基硅氧烷产物按比例转移到随后的第二阶段的反应蒸馏塔af 平均停留时间为0.5至180分钟; 在反应蒸馏塔中的第二阶段进行反应和蒸馏，其中挥发性成分从塔顶排出，有机烷氧基硅氧烷产物作为底部产物排出，其中反应蒸馏塔在底部温度为50℃ 至200℃

125. 发明授权

US5468706A Storage-stable solution of a mixture of carbonated magnesium methoxide, carbonated magnesium ethoxide and their carbonated mixed alkoxide in a combination of methanol and ethanol and uses thereof 失效
标题翻译：碳酸化甲醇镁，碳酸化乙醇镁和它们的碳酸化混合醇盐的混合物与甲醇和乙醇的组合的储存稳定溶液及其用途
公开(公告)号：US5468706A
公开(公告)日：1995-11-21
申请号：US167354
申请日：1993-12-15
申请人： Hartwig Rauleder , Burkhard Standke , Hans-Joachim Kotzsch , Reinhold Schork
发明人： Hartwig Rauleder , Burkhard Standke , Hans-Joachim Kotzsch , Reinhold Schork
IPC分类号： C07C29/94 , C07C29/68 , C07C31/30 , C08F4/02 , C08F4/50 , C08F4/60 , C08F4/654 , C08F10/00 , D21H25/02 , D21H25/18 , C07F3/02 , B01J31/12 , D21H17/12
CPC分类号： D21H25/18 , C07C29/68 , C07C31/30 , C08F10/00
摘要： The present invention relates to a storage-stable solution of a mixture of carbonated magnesium methoxide of the formula Mg(CH.sub.3 O).sub.2 (CO.sub.2).sub.n, carbonated magnesium ethoxide of the formula Mg(C.sub.2 H.sub.5 O).sub.2 (CO).sub.2).sub.n and a carbonated mixed alkoxide of the formula Mg(CH.sub.3 O).sub.x (C.sub.2 H.sub.5 O).sub.y (CO.sub.2).sub.n, in which 0
摘要翻译：本发明涉及式Mg（CH 3 O）2（CO 2）n的碳酸化甲醇镁，式Mg（C 2 H 5 O）2（CO）2）n的碳酸化的乙醇镁和碳酸化的甲醇和乙醇的组合，其中0

126. 发明授权

US5107009A Process for the preparation of mercaptosilanes 失效
标题翻译：制备杀虫剂的方法
公开(公告)号：US5107009A
公开(公告)日：1992-04-21
申请号：US738348
申请日：1991-07-31
申请人： Hartwig Rauleder , Claus-Dietrich Seiler , Hans-Joachim Kotzsch , Burkhard Standke
发明人： Hartwig Rauleder , Claus-Dietrich Seiler , Hans-Joachim Kotzsch , Burkhard Standke
IPC分类号： C07F7/18
CPC分类号： C07F7/1892
摘要： Mercaptosilanes are prepared from haloorganylsilyl compounds and an alkali metal hydrogen sulfide in the presence of a polar, aprotic medium.
摘要翻译：巯基硅烷由卤代有机基甲硅烷基化合物和碱金属硫化氢在极性非质子介质存在下制备。

127. 发明授权

US4717562A Pure silver (III) oxide 失效
标题翻译：纯银（III）氧化物
公开(公告)号：US4717562A
公开(公告)日：1988-01-05
申请号：US37970
申请日：1987-04-14
申请人： Martin Jansen , Burkhard Standke
发明人： Martin Jansen , Burkhard Standke
IPC分类号： C25B1/00 , C01G5/00
CPC分类号： C25B1/00
摘要： Silver salts, preferably AgClO.sub.4, AgBF.sub.4, and AgPF.sub.6 are oxidized electrolytically at -15.degree. to +10.degree. C. and a pH between 4.5 and 7.5 with a current density of 40 to 200 A/m.sup.2 to produce pure silver (III) oxide.
摘要翻译：银盐，优选AgClO 4，AgBF 4和AgPF 6在-15℃至+ 10℃下电解氧化，pH在4.5至7.5之间，电流密度为40至200A / m 2，以产生纯的氧化银（III）。

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