2530-85-0Relevant academic research and scientific papers
A high-quality γ - methyl methacryloxy propyl trimethoxy silane preparation method (by machine translation)
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Paragraph 0031; 0039; 0040, (2018/09/08)
The invention relates to a high-quality γ - methyl methacryloxy propyl trimethoxy silane preparation method, which belongs to the technical field of organic chemistry, this invention has improved the allyl methacrylate silanes with three a oxygen radical hydrogen addition of hydrogen synthesis method, such as compression, excessive use of three a oxygen radical hydrogen silane and anti-feeding mode, γ - methyl through propyl trimethoxy silane preparation method a series of improved, to obtain a high-quality synthetic route, through the above-mentioned improved, compared with the original process, γ - methyl methacryloxy propyl trimethoxy silane is obviously improved yield, basic are kept in a 93% or more, and the rectification of the residual high [...] reduce. (by machine translation)
Process for manufacturing polysiloxane microcapsules that are functionalized and are not very porous
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Page/Page column 4, (2016/09/26)
A method is provided for encapsulating products that can have lipophilic or hydrophilic, including volatile, properties in a polysiloxane membrane that is particularly impervious. A method is also provided for evaluating the imperviousness of capsules. The present method includes the following steps: a) formation of droplets by an emulsion between an oily phase containing the product to be encapsulated and an acidic aqueous phase heated to around 50° C. and in the presence of surfactants; b) addition and hydrolysis of at least one silane in order to obtain a silanol; c) increasing the pH in order to start condensation of the silanol to form a first membrane around the droplets of the product to be encapsulated; d) lowering the pH; e) increasing the pH, optionally preceded by adding a silane, in order to obtain a new condensation of silanol around the droplets of the product to be encapsulated.
Method for preparing organic silicon by passage reaction device
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Paragraph 0050, (2016/10/17)
The invention provides a method for preparing organic silicon by a passage reaction device. Under the condition of main catalysts Z, hydrogen-containing silane X and an unsaturated compound Y are introduced into the passage reaction device; hydrosilylation reaction is performed to prepare the organic silicon, wherein the hydrogen-containing silane X has the structure being HSiRR'Cl, in the formula, R and R' are independently C1 to C16 alkyl or alkoxy; a=1, 2 or 3; b, c and d are respectively and independently 0, 1, 2 or 3; the unsaturated compound Y is a monoene compound or single-alkyne compound; the main catalysts Z are one or several mixed ones of single-component complexes or multi-component complexes of Pt, Pd, Rh, Ru, Cu, Ag, Au or Ir; the passage surface in which reaction flow contacts is subjected to inactivation treatment by an activating agent Z. The problems of long reaction period, poor stability and the like of large-sized reaction equipment are solved; the problem that mixing, pre-reaction and afterreaction are separated and are performed in multi-unit equipment is solved.
COSMETIC TREATMENT METHOD COMPRISING THE APPLICATION OF A COATING BASED ON AN AEROGEL COMPOSITION OF LOW BULK DENSITY
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Paragraph 0070, (2014/02/15)
The present invention relates to a cosmetic treatment method comprising the formation of a coating on keratin fibres characterized in that it comprises: 1) the preparation of an aerogel precursor composition comprising:—at least one organic solvent chosen from acetone, C1-C4 alcohols, C1-C6 alkanes, C1-C4 ethers, which may or may not be perfluorinated, and mixtures thereof and at least one precursor compound that contains:—at least one atom chosen from silicon, titanium, aluminium and zirconium,—at least one hydroxyl or alkoxy function directly attached to the atom chosen from silicon, titanium, aluminium and zirconium by an oxygen atom, and,—optionally an organic group directly attached to the atom chosen from silicon, titanium, aluminium and zirconium by a carbon atom, 2) the removal of the solvent or solvents resulting in the formation of an aerogel composition having a bulk density less than or equal to 0.35 g/cm3, 3) the application to the keratin fibres of the aerogel composition resulting from step 2) or of the aerogel precursor composition resulting from step 1). Advantageously, the molar ratio between the precursor compounds and the solvent is at most 1/20.
METHOD OF PRODUCING A HYDROLYZABLE SILICON-CONTAINING COMPOUND
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Page/Page column 22; 24, (2012/07/14)
The present invention provides a safe, inexpensive, and high yield means of producing a hydrolyzable silicon-containing compound, e.g., an organooxysilane and the like. A compound (A) represented by the general formula R1-O-R2 wherein R1 represents a C4-30, substituted or unsubstituted, tertiary alkyl group or aralkyl group and R2 represents a C1-30, substituted or unsubstituted, monovalent hydrocarbyl group or acyl group, is reacted in the presence of a Lewis acid catalyst with a halosilane (B) represented by the general formula R3mSiX4-m wherein R3 represents the hydrogen atom or a C1-30 substituted or unsubstituted monovalent hydrocarbyl group, X is independently bromine or chlorine, and m represents an integer from 0 to 3.
Practical conversion of chlorosilanes into alkoxysilanes without generating HCl
Wakabayashi, Ryutaro,Sugiura, Yasushi,Shibue, Toshimichi,Kuroda, Kazuyuki
supporting information; experimental part, p. 10708 - 10711 (2011/12/05)
Alcohol-free: A versatile, efficient, and practical synthesis of alkoxysilanes without generation of HCl involves the reaction of chlorosilanes with unsymmetrical ethers in the presence of a Lewis acid (see scheme). The reaction proceeds through selective cleavage of C-O bonds and is superior to conventional processes. Industrially feasible reagents are used and only one by-product results. Copyright
SYSTEM, REACTOR AND PROCESS FOR CONTINUOUS INDUSTRIAL PREPARATION OF 3-METHACRYLOYLOXYPROPYLALKOXYSILANES
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Page/Page column 6-7, (2010/08/03)
The present invention relates to a system, to a reactor and to a process for continuous industrial performance of a reaction wherein allyl methacrylate A is reacted with an HSi compound B in the presence of a catalyst C and optionally of further assistants, and the system is based at least on the combination of reactants (3) for components A (1) and B (2), at least one multielement reactor (5) which, in turn, comprises at least two reactor units in the form of exchangeable pre-reactors (5.1) and at least one further reactor unit (5.3) connected downstream of the pre-reactors, and on a product workup (8).
Some regularities of chlorosilanes etherification
Belyakova,Komarov,Bykovchenko,Ershov,Chernyshev,Storozhenko
body text, p. 1650 - 1655 (2011/05/13)
The influence of reagents, solvent polarity, and temperature on the etherification of chlorosilanes ClCH2SiCl3, VinSiCl 3, PrSiCl3, and Ph3SiCl with ethanol was studied. Influence of reaction temperature on the ratio of the synthesized alkoxysilane and related side-product siloxane is revealed. Use of excess alcohol is shown to increase the content of siloxane. Introduction of FeCl 3 does not affect the synthesis. Solvents are shown to influence the reaction rate: the rate constant increases with increasing ε parameter of the solvent. The rate constant of etherification of chlorosilanes with ethanol falls in the series: ClCH2SiCl3 > VinSiCl3 > PrSiCl3. An explanation of the regularities is suggested.
A METHOD OF MANUFACTURING AN ORGANIC SILICON COMPOUND THAT CONTAINS A METHACRYLOXY GROUP OR AN ACRYLOXY GROUP
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Page/Page column 11, (2008/06/13)
A method of manufacturing an organic silicon compound that contains a methacryloxy group or an acryloxy group, the method being characterized by the fact that manufacturing or conducting purification by distillation is carried out in the presence of a phenothiazine derivative having a molecular weight equal to or higher than 240. And a stable composition comprising an organic silicon compound that contains a methacryloxy group or an acryloxy group and a phenothiazine derivative having a molecular weight equal to or higher than 240 and used in an amount sufficient to stabilize the aforementioned organic silicon compound.
PROCESS FOR PRODUCING ORGANOALKOXYSILANES FROM ORGANIC ACIDS OR CYANATES AND HALOALKYLALKOXYSILANES
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Page/Page column 4, (2010/11/25)
A process for the preparation of organoalkoxysilanes containing one or more organic functional groups derived from organic acids or hydrogen cyanates, by a continuous or batch process utilizing a solid guanidinium salt as a phase transfer catalyst for the reaction between a liquid phase haloalkylalkoxysilane and a solid phase alkali or alkaline earth metal salt or ammonium salt of an organic acid or a metal cyanate.
