摘要:
The invention relates to a method for the treatment of a composition containing inorganic silanes and at least one foreign metal and/or a compound containing a foreign metal, wherein the composition is brought in contact with at least one adsorption agent, and for obtaining the composition, in which the content of foreign metal and/or of a compound containing a foreign metal is reduced, and to a corresponding composition having a reduced foreign metal content, and further to the use of organic resins, activated carbons, silicates, and/or zeolites for the reduction of foreign metals and/or compounds containing foreign metals in compositions of inorganic silanes.
摘要:
The present invention relates to a specific process for preparing organosilane esters of the formula (I) and a composition comprising more than 98% by weight of organosilane esters of the formula (I) and less than 2.0% by weight of at least one hydrocarbon and to the use of such a composition as precursor for producing a layer or film having a dielectric constant of 1
摘要:
A process for preparing epoxysilanes by reacting a hydrogensilane with an allyl glycidyl ether in the presence of a catalyst and working up the crude product obtained, where the catalyst is removed from the crude product and the crude product is subsequently distilled.
摘要:
Particulate magnesium ethoxide having a high coarse particle content can be obtained in a simple and economical manner by the present invention, which provides a process for preparing particulate magnesium ethoxide having a coarse grain content, and includes reacting metallic, optionally activated, magnesium with liquid ethanol under pressure at a temperature above 78° C. The present invention also relates to particulate magnesium ethoxide having a coarse grain content, which contains: 500 &mgr;m.
摘要:
A process for the continuous preparation of 3-halopropylorganosilanes of the general structure RbH3-a-bXaSiCH2CH2CH2Y (III), where: R is CH3, C2H5, C3H7, OCH3, OC2H5 or OC3H7, X is F, Cl, Br or I, Y is F, Cl, Br or I, and a and b are each one of the numbers 0, 1, 2 or 3 and the sum a+b is 1, 2 or 3, comprising reacting, as starting materials, an allyl halide with a silane carrying at least one H atom, wherein the starting materials are present in stoichiometric amounts or one of the starting materials is present in substoichiometric amounts, wherein the reaction carried out is a partial reaction of from 10% to 80%, on a molar basis, of the starting materials, based on either material, when both are present in stoichiometric amounts, or based on the substoichiometric material.
摘要翻译:连续制备通常结构的3-卤代丙基有机硅烷的方法,其中R为CH 3,C 2 H 5,C 3 H 7,OCH 3,OC 2 H 5或OC 3 H 7,X为F,Cl,Br或I,Y为F,Cl,Br或I, 和b分别为数字0,1,2或3中的一个,并且和a + b为1,2或3,包括使烯丙基卤化物与携带至少一个H原子的硅烷作为原料,其中, 原料以化学计量的量存在,或者一种起始原料以亚化学计量的量存在,其中进行的反应是基于摩尔的10%至80%的起始原料的部分反应,基于任一材料 ,当两者都以化学计量的量存在时,或基于亚化学计量的材料。
摘要:
Acyloxysilanes are prepared by a process of reacting an organochlorosilane with an excess of monocarboxylic anhydride at elevated temperature, thereby forming product acyloxysilane and by-product acyl chloride transferring the reaction mixture to the middle inlet of a separation tower having a still pot at its base, removing excess carboxylic anhydride by distillation at the tower top under reduced pressure, removing acyl chloride by-product from the separation tower, uniformly removing acyloxysilane from the tower still pot, and reacting virtually quantitatively the residual acid chloride present in the acyloxysilane removed from the still pot by adding a metal carboxylate to the acyloxysilane and separating the metal chlorides formed from the product.
摘要:
A process for removing residual acidic chlorine from acyloxysilanes, comprises virtually quantitatively reacting metal carboxylates with the acidic chlorine present in the acyloxysilane, and the metal chlorides formed being separated off.
摘要:
The present invention relates to a storage-stable solution of carbonated magnesium methoxide of the formula Mg(CH.sub.3 O).sub.2 (CO.sub.2).sub.n in methanol, and processes for their preparation by reacting metallic magnesium with methanol and CO.sub.2 or reacting magnesium methoxide in methanol with CO.sub.2, wherein the magnesium content of the solution is from 0.1 to 8% by weight, based on the total weight of the solution, and the CO.sub.2 content n is from 1 to 2.2. The present solution is used, inter alia, for the preservation of paper or for the preparation of a catalyst for the polymerization of olefins.
摘要:
The invention involves spherical particles of magnesium alkoxide and a process for their preparation. Specifically, spherical magnesium alkoxide is produced by spray drying of an alcoholic solution of the corresponding carboxylated magnesium alkoxide and subsequent drying and decarboxylation, characterized in that the solution is sprayed via a two-material nozzle with inner atomization, which is operated in the part-load range at 10 to 30% of its capacity, into an inert accompanying gas which is under a pressure of 1.0 to 1.2 bar, has been preheated to 100.degree.-140.degree. C. and is fed cocurrently, after which the resulting finely divided carboxylated magnesium alkoxide is dried and is decarboxylated. The magnesium alkoxide is used for the preparation of a catalyst for the polymerization of .alpha.-olefins.
摘要:
Monoalkylethers of alkyleneglycols and oligoalkyleneglycols are reacted completely with terminally unsaturated alkenyl halides to form terminally mono unsaturated glycolethers as product, wherein initially a complete reaction to the corresponding alcoholate takes place with only one equivalent of alcoholate former, such as alkali metal alcoholate or hydroxide, and two equivalents of glycolmonoether, then the alcoholate is reacted with one equivalent of alkenyl halide, whereupon a mixture of the desired product and the glycolmonoether of the alkali metal halide is filtered or distilled off, then this mixture is reacted with the second equivalent of the alcoholate former, whereupon the recovery of the product takes place by distillation from the reaction mixture and then, after addition of a further equivalent of glycolmonoether to the residue from the product recovery, the reaction of the first and the subsequent steps is repeated.