EP2758409A1 - Procédé de production de poudres à base de sels alcalins de silanols - Google Patents

Procédé de production de poudres à base de sels alcalins de silanols

Info

Publication number
EP2758409A1
EP2758409A1 EP12756713.9A EP12756713A EP2758409A1 EP 2758409 A1 EP2758409 A1 EP 2758409A1 EP 12756713 A EP12756713 A EP 12756713A EP 2758409 A1 EP2758409 A1 EP 2758409A1
Authority
EP
European Patent Office
Prior art keywords
hydrolysis
condensation products
water
ome
alcohol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP12756713.9A
Other languages
German (de)
English (en)
Inventor
Michael Stepp
Michael Mueller
Birgit Peschanel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wacker Chemie AG
Original Assignee
Wacker Chemie AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Wacker Chemie AG filed Critical Wacker Chemie AG
Publication of EP2758409A1 publication Critical patent/EP2758409A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0834—Compounds having one or more O-Si linkage
    • C07F7/0836—Compounds with one or more Si-OH or Si-O-metal linkage
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0834—Compounds having one or more O-Si linkage
    • C07F7/0838—Compounds with one or more Si-O-Si sequences

Definitions

  • the invention relates to a process for the preparation of
  • Alkoxyl organosiliconates such as potassium methylsiliconate, have been used for decades for hydrophobing, in particular of
  • Ready-to-use building material mixtures such as cement or gypsum plasters and putties or tile adhesives are mainly delivered as powder in bags or silos to the construction site and only there with the mixing water touched.
  • the ready-to-use building material mixtures such as cement or gypsum plasters and putties or tile adhesives are mainly delivered as powder in bags or silos to the construction site and only there with the mixing water touched.
  • the ready-to-use building material mixtures such as cement or gypsum plasters and putties or tile adhesives
  • Organosiliconates in solid form have proven to be very efficient hydrophobizing additives. Their use is described, for example, in the following documents:
  • US 2567110 describes access to neutral (poly) siloxanes starting from alkali metal (ox) anolates and chlorosilanes.
  • Example 1 describes the preparation of sodium methylsiliconate by reacting a monomethylsiloxane hydrolyzate with one molar equivalent of sodium hydroxide solution in the presence of ethanol. The solid is isolated by distilling off the solvent and then dried at 170 ° C to constant weight. On a technical scale, such a method for solid insulation is not feasible, since in
  • Solvents are present.
  • Alkalisiliconate very much energy for the evaporation of the solvent water is needed, which is the Wirtschaf probability of the process
  • the hydrates are obtained as siliconates by evaporation of the alcohol or by addition
  • Example 1 the preparation of solid
  • alkali metal hydroxide aqueous solution of alkali siliconate, which is stabilized by the addition of up to 10% alcohol or ketone. How the drying of the siliconate takes place is not described. The application of the dried
  • Siliconate for the hydrophobization of gypsum is called.
  • the invention relates to a process for the preparation of powders (P) from salts of silanols, of which
  • Hydrolysis / condensation products or alkoxysilanes together with their hydrolysis / condensation products, wherein the alkoxy group is selected from methoxy, ethoxy, 1-propoxy and 2-propoxy group, hydrolyzed with alkali hydroxide and water,
  • the process differs from the prior art by a stepwise drying process.
  • the prerequisite for carrying out the process is that the alcohol present in the hydrolyzate has a lower boiling point than water, i. is selected from methanol, ethanol, 1-propanol or 2-propanol.
  • salts of organosilanols are prepared in the process, wherein in the first step organoalkoxysilanes of the general formula 1 (R x ) a Si (OR 4 ) b (-Si (R 2 ) 3 - c (OR 4 ) c ) d (D or their Hydrolysis / condensation products, or the
  • R 3 is hydrogen, a monovalent unsubstituted or substituted by halogen atoms or NH 2 groups
  • Hydrocarbon radical having 1 to 8 carbon atoms Hydrocarbon radical having 1 to 8 carbon atoms
  • R 4 is methoxy, ethoxy, 1-propoxy or 2-propoxy
  • a is the values 1, 2 or 3 and
  • b, c, d are 0, 1, 2 or 3
  • Oligomers can be used from compounds of general formula 1, or mixtures of these mixed oligomeric siloxanes with monomeric silanes of general formula 1. Where appropriate, existing silanol groups formed by hydrolysis in the compounds of general formula 1 or their oligomers do not interfere.
  • Tetraalkoxysilanes and / or their
  • Organoalkoxysilanes of the general formula 1 and / or their hydrolysis / condensation products are used.
  • R 1 , R 2 may be linear, branched, cyclic, aromatic, saturated or unsaturated. May be C e alkyl, cycloalkyl, aryl, arylalkyl, alkylaryl, which may be substituted by - Examples of amino groups in R 1, R 2 are radicals -NR S R 6 wherein R 5 and R 6 is hydrogen, a radical C -OR 7 , where R 7 is C 1 -C 8 -alkyl, aryl, Arylalkyl, alkylaryl can be. If R s , R 6 are alkyl radicals, non-adjacent CH 2 units may be replaced by groups -O-, -S-, or -NR 3 -. R 5 and R 6 may also be a cycle. R 5 is preferably hydrogen or an alkyl radical having 1 to 6 carbon atoms,
  • R 1 , R 2 in the general formula 1 is preferably a monovalent unsubstituted or substituted by halogen atoms, amino, alkoxy or silyl hydrocarbon radical having 1 to 18 carbon atoms. Particularly preferred are unsubstituted alkyl radicals, cycloalkyl radicals, alkylaryl radicals, arylalkyl radicals and phenyl radicals.
  • the alkyl radicals cycloalkyl radicals, alkylaryl radicals, arylalkyl radicals and phenyl radicals.
  • Hydrocarbon radicals R 1 , R 2 1 to 6 carbon atoms particularly preferred are the methyl, ethyl ⁇ , propyl, 3,3,3-trifluoropropyl, vinyl and phenyl, especially the methyl radical.
  • radicals R 1 , R 2 are:
  • R 1 , R 2 are radicals - ⁇ CH 2 O) n -R 8 , - (CH 2 CH 2 0) m -R 9 , and - (CH 2 CH 2 NH) 0 H, where n, m and o are from 1 to 10, in particular 1, 2, 3 and R 8 , R 9 have the meanings of R 5 , R 6 .
  • R 3 is preferably hydrogen or a
  • R 3 are listed above for R 1 .
  • d is 0.
  • at most at 20 mol%, in particular at most 5 mol% of the compounds of general formula 1 d is 1, 2 or 3.
  • MeSi (OMe) 3 MeSi (OEt) 3 , MeSi (OMe) 2 (OEt), MeSi (OMe) (OEt) 2 ,
  • MeSi (OMe) 3 MeSi (OEt) 3 , (H 3 C) 2 CHCH 2 -Si (OMe) 3 and PhSi (OMe) 3 , where methyltrimethoxysilane or its
  • Hydrolysis / condensation product are particularly preferred.
  • MeCl 2 SiSiMeCl 2 Me 2 Si (OMe) Si (OMe) 3 , Me 2 Si (OMe) Si (OMe) Me 2 ,
  • Me 2 Si (OMe) SiMe 3 Me 2 Si (OMe) SiMe (OMe) 2 .
  • Me 2 Si (OMe) 2i Me 2 Si (OEt) 2 MeSi (OMe) 2 CH 2 CH 2 CH 3
  • Ph-Si (OMe) 2 Me wherein Me 2 Si (OMe) 2 and MeSi (OMe ) 2 CH 2 CH 2 CH 3
  • Me is methyl
  • Et is ethyl
  • Ph is phenyl
  • t-Bu is 2, 2-dimethylpropyl
  • cy-Hex means cyclohexyl
  • hexadecyl means n-hexadecyl.
  • A is preferably 1 or 2. In particular, at least 50%, preferably at least 60%, particularly preferably at least 70% and at most 100%,
  • the alkali hydroxide used is preferably selected from lithium, sodium and potassium hydroxide.
  • the amount of alkali hydroxide is preferably chosen such that the cation to silicon molar ratio is at least 0.2,
  • At least 0.4 more preferably at least 0.5, particularly preferably at least 0.6 and at most 2.0, preferably at most 1.0, particularly preferably at most 0.8, more preferably at most 0, 7.
  • suspensions may also be used in which silanolate salt is undissolved. It is also possible to dry mixtures of alcoholic-aqueous mixtures of different silanolate salts by the process according to the invention, it being possible for one or more alcohols to be present. Step 2 has the aim of maximizing the proportion of
  • step 3 preferably residual alcohol and the existing or during the drying process
  • step 2 optionally water formed by condensation processes, but preferably at the same temperature as in step 2 but removed under reduced pressure. Preferably, this contributes to a residual moisture content in a measurement
  • both steps are under exclusion of oxygen, in particular under one
  • Inertgasatmospreheat for example, from nitrogen, argon, helium, performed, If in the first step organoalkoxysilanes of the general formula 1 are used, the drying or
  • Wall temperature i. the highest temperature with which the mixture to be dried comes into contact, preferably chosen such that thermal decomposition of the reaction mixture within the entire drying time in the steps 2 and 3
  • the drying or wall temperature is preferably selected so that the TMR ad is at least 200%, preferably at least 150%, particularly preferably at least 100% of the drying time. This results in the maximum amount of distillate available in step 2: at higher temperatures, a larger amount of distillate is obtained than at lower temperatures. To achieve a high space-time yield, it is therefore desirable to achieve the highest possible temperature in step 2.
  • the drying or wall temperature is preferably selected so that the TMR ad is at least 200%, preferably at least 150%, particularly preferably at least 100% of the drying time. This results in the maximum amount of distillate available in step 2: at higher temperatures, a larger amount of distillate is obtained than at lower temperatures. To achieve a high space-time yield, it is therefore desirable to achieve the highest possible temperature in step 2.
  • the drying or wall temperature is preferably selected so that the TMR ad is at least 200%, preferably at least 150%, particularly preferably at least 100% of the drying time. This results in the maximum amount of distillate available in step 2: at higher temperatures
  • Wall temperature in step 2 and 3 at least 70 ° C, more preferably at least 90 ° C, in particular at least 100 ° C and preferably at most 200 ° C, more preferably at most 160 ° C, in particular at most 140 ° C, provided that no disturbing thermal decomposition in these Temperatures occurs.
  • the temperature may remain constant during step 2 or it may undergo an ascending or descending gradient, with an increasing gradient being preferred.
  • the achievable degree of drying in step 3 is determined by the
  • the drying or wall temperature preferably moves in the area mentioned for step 2, but it can be higher or lower or go through an ascending or descending gradient.
  • the pressure in step 3 is chosen as low as possible in order to keep the duration of the drying as small as possible and thus to maximize the space-time yield. It is preferably at most 200 hPa, preferably at most 100 hPa, particularly preferably at most 50 hPa,
  • Step 2 is generally particularly preferred at a higher pressure than step 3, preferably at least 500 hPa above the pressure of step 3
  • step 3 at least 700 hPa above the pressure of step 3, especially under the pressure established by inert gas ventilation of the apparatus, i. Overpressure of at most 5 hPa compared to atmospheric pressure carried out.
  • steps 2 and 3 are carried out in a single apparatus, e.g. Batch reactor such as agitator or paddle dryer, carried out sequentially, the pressure during the transition from step 2 to step 3 is preferably not abruptly reduced to
  • steps 2 and 3 are each carried out in a separate apparatus, so the transition from one to the other apparatus with a
  • step 2 It may also undergo a pressure gradient from the beginning of the drying in step 2 to the end of the drying in step 3 This procedure is recommended, for example, for an automated time-optimized batch process.
  • a gas eg inert gas such as nitrogen or steam, eg water vapor, is an additional possibility for the drying process both in step 2 and in step 3 accelerate.
  • the process may be run in batch mode, e.g. using a stirred tank or paddle dryer with distillation head, as is common in multi-purpose plants, carried out.
  • direct heating e.g. by means of
  • Microwave heating, firing / hot gas heating it is in the case of indirect heat transfer by heat transfer, for example, water vapor, water, heat transfer oil, procedurally and for reasons of time cheaper if steps 2 and 3 run at the same temperature.
  • a continuous process in a tube reactor or a mixing / delivery unit such as a kneader or a single-screw or twin-screw extruder or a horizontal paddle dryer - preferably with multiple chambers for the various process steps - is also possible and advantageous for large-scale production.
  • a mixing / delivery unit such as a kneader or a single-screw or twin-screw extruder or a horizontal paddle dryer - preferably with multiple chambers for the various process steps - is also possible and advantageous for large-scale production.
  • To avoid foaming is preferably in step 2, in particular in the pressure reduction in step 3 a
  • Antifoam e.g. a silicone oil, a surfactant or a defoamer mixture of fumed silica and
  • defoamer additive is preferably at most 3 wt .-%, more preferably at most 1 wt .-%, in particular at most 0.5 wt .-% based on the starting mixture used in step 2.
  • other additives such as e.g. flow aids,
  • Anti-caking agents are added before, during or after the inventive process.
  • Compacted particles or moldings e.g. Granules, briquettes, and then classified or classified,
  • Formulas is the silicon atom tetravalent. in the following Examples and Comparative Examples, unless stated otherwise, all amounts and
  • Example 1 Inventive three-stage process for
  • step 1 a hydrolyzate H1 analogous to Example 1 in DE 4336600 from one molar equivalent of methyltrimethoxysilane (prepared from 1 molar equivalent of methyltrichlorosilane and 2 * 1.5 molar equivalents of methanol), 0.65 molar equivalents
  • Solid content 42% by weight (determined with the solid-state balance HR73 Halogen Moisture Analyzer from Mettler Toledo at 160 ° C., contains 44.5% by weight of methanol and 13.5% by weight of water according to NMR).
  • TMR ad time to maximum rate
  • Activation energy is calculated for different temperatures, the TMR a d. Accordingly, a TMR ad of> 24 h results at 118 ° C.,> 20 h at 120 ° C. and> 8 h at 130 ° C.
  • hydrolyzate H1 400 g of hydrolyzate H1 are initially introduced into the distillation bridge and 0.12 g of silicone oil AK 100 (commercially available from WACKER CHEMIE AG) are added as defoamer additive.
  • Step 2 the stirrer is set to 230 rpm and the reactor jacket is charged with the heat transfer oil heated to 120 ° C. by means of a thermostat. The contents of the reactor warm up and begin to boil at 71 ° C. During the distillate decrease, the boiling temperature rises to 77 ° C, then the amount of distillate drops. A total of 89.2 g of clear, colorless condensate are collected within 20 minutes, which is loud
  • Methanol content and about 10% of the total water content.
  • Step 3 At 120 ° C jacket temperature, the pressure is gradually reduced by means of a vacuum pump to 5 hPa, while volatile constituents are condensed. The viscous, cloudy
  • Distillation residue from step 1 turns visibly into a white-foamy viscous mass and finally turns into a fine dry powder.
  • the template collects within 30 minutes 144.4 g of clear colorless distillate, which contains 67.6% methanol and 32.4% water by gas chromatographic analysis. This corresponds to approx. 55% of the total methanol content and approx. 87% of the total water content.
  • the solids content is 99.4% (determined with the Festgehaltswaage HR73 Halogen Moisture Analyzer from Mettler Toledo at 160 ° C) and dissolves 50% in water.
  • Example 2 Inventive three-stage process for
  • Distillation bridge 40 g of Kaliumisobutylsiliconat- solution from a) are presented.
  • Step 2 the stirrer is set to 230 rpm and the reactor jacket is charged with the heat carrier oil heated to 120 ° C. The reactor contents warm up and start at
  • Step 3 At 120 ° C jacket temperature, the pressure is reduced by means of a vacuum pump within 30 minutes to 5 hPa, while volatile constituents are condensed. The jelly-like distillation residue from step 2 rapidly turns into individual brittle particles and finally turns into a fine dry powder. After another 30 minutes at 120 ° C
  • thermometer and distillation bridge with template 120 g of hydrolyzate HI according to Example 1 and 0.04 g of silicone oil AK 100 (commercially available
  • Vacuum pump the pressure is reduced so that the temperature of the mixture between 50 ° C and 60 ° C can be maintained.
  • Condensate collects in the original and in the liquid Nitrogen cooled cold trap. After 16 minutes 220 hPa are reached, the mixture cooled to 50 ° C begins to foam, at the same time a sticky wall covering forms, which visibly agglomerates into a large lump, which disintegrates into smaller fragments only after cutting with a spatula Hour at 5 hPa and 120 ° C
  • Solids content is 99.8% (determined by the
  • Solids content 44.3% by weight (determined with the solids balance HR73 Halogen Moisture Analyzer from Mettler Toledo at 160 ° C., contains 42.3% by weight of methanol and 13.4% by weight of water according to NMR) and 0.04 g of silicone oil AK 100 (commercially available from WACKER CHEMIE AG) as an antifoam additive.
  • the flask is heated by an oil bath heated to 50 ° C. through
  • Vacuum pump the pressure is reduced to 5 hPa.
  • Oil bath temperature reached the internal temperature is 5 ° C. From the viscous swamp settle solid wall coverings. After a further 10 minutes, the oil bath has a temperature of 70 ° C and the internal temperature is 10 ° C, the viscous mass wraps around the stirrer, it is stirred for one hour at 120 ° C oil bath temperature and 5 hPa and receives only after extensive mechanical fragmentation with a spatula 57 g of a white, sticky compact solid, the solids content of which is 91.9% (determined with the fixed weight scale HR73 Halogen Moisture Analyzer Mettler Toledo at 160 ° C).
  • Methanol is obviously not condensed and disappears via the exhaust path.
  • thermometer and distillation bridge with template 120 g are analogs
  • Example 1 prepared hydrolyzate Hl and 0.04 g of silicone oil AK 100 (commercially available from WACKER CHEMIE AG) presented as defoamer additive. The piston is heated to 70 ° C
  • Temperature of the mixture is between 50 and 60 ° C. Condensate collects in the receiver and in the liquid nitrogen cooled cold trap. At 200 hPa, the contents start to foam strongly and a wall coating forms. At 50 hPa, the tacky residue contracts around the stirrer shaft. The mixture is stirred for an hour at 120 ° C oil bath temperature and 5 hPa and receives only after extensive mechanical fragmentation with a spatula 56.7 g of a white, sticky, grainy

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)

Abstract

L'invention concerne un procédé de production de poudres (P) à base de sels de silanols, de leurs produits d'hydrolyse/de condensation, ou de silanols conjointement avec leurs produits d'hydrolyse/de condensation et de cations qui sont choisis parmi des ions alcalins, dans lesquels le rapport molaire du cation au silicium va de 0,1 à 3, selon lequel, dans une première étape, des alcoxysilanes, leurs produits d'hydrolyse/de condensation, ou des alcoxysilanes conjointement avec leurs produits d'hydrolyse/de condensation, le groupe alcoxy étant choisi parmi un groupe méthoxy, éthoxy, 1-propoxy et 2-propoxy, sont hydrolysés avec de l'hydroxyde alcalin et de l'eau. Dans une deuxième étape, à partir de l'hydrolysat produit dans la première étape, au moins 20 pour cent en poids au total de l'eau et de l'alcool présents dans l'hydrolysat sont éliminés par distillation ; et dans une troisième étape, l'eau et l'alcool restants sont éliminés à une pression plus basse que dans la deuxième étape.
EP12756713.9A 2011-09-21 2012-09-07 Procédé de production de poudres à base de sels alcalins de silanols Withdrawn EP2758409A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102011083109A DE102011083109A1 (de) 2011-09-21 2011-09-21 Verfahren zur Herstellung von Pulvern aus Alkalisalzen von Silanolen
PCT/EP2012/067462 WO2013041385A1 (fr) 2011-09-21 2012-09-07 Procédé de production de poudres à base de sels alcalins de silanols

Publications (1)

Publication Number Publication Date
EP2758409A1 true EP2758409A1 (fr) 2014-07-30

Family

ID=46829749

Family Applications (1)

Application Number Title Priority Date Filing Date
EP12756713.9A Withdrawn EP2758409A1 (fr) 2011-09-21 2012-09-07 Procédé de production de poudres à base de sels alcalins de silanols

Country Status (7)

Country Link
US (1) US20140228589A1 (fr)
EP (1) EP2758409A1 (fr)
JP (1) JP2014530196A (fr)
KR (1) KR20140054285A (fr)
CN (1) CN103827125A (fr)
DE (1) DE102011083109A1 (fr)
WO (1) WO2013041385A1 (fr)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2817256A1 (fr) 2010-11-12 2012-05-18 The General Hospital Corporation Arn non codants associes a polycomb
US9920317B2 (en) 2010-11-12 2018-03-20 The General Hospital Corporation Polycomb-associated non-coding RNAs
DE102011086812A1 (de) 2011-11-22 2013-05-23 Wacker Chemie Ag Verfahren zur Herstellung von Feststoffen aus Alkalisalzen von Silanolen
CN103408575B (zh) * 2013-08-28 2016-06-15 淄博市临淄齐泉工贸有限公司 丙基硅酸盐防水剂的制备方法
DE102014205258A1 (de) 2014-03-20 2015-09-24 Wacker Chemie Ag Verfahren zur Herstellung von Pulvern aus Alkalisalzen von Silanolen
DE102014209583A1 (de) 2014-05-20 2015-11-26 Wacker Chemie Ag Verfahren zur Herstellung von Pulvern aus Alkalisalzen von Silanolen
DE102014212698A1 (de) 2014-07-01 2016-01-07 Wacker Chemie Ag Verfahren zur Herstellung von Siloxanen aus Alkalisalzen von Silanolen
US10100024B2 (en) 2014-07-29 2018-10-16 Evonik Degussa Gmbh Process for the epoxidation of an olefin
WO2016070060A1 (fr) 2014-10-30 2016-05-06 The General Hospital Corporation Procédés de modulation de la répression génique dépendant d'atrx
DE102015204263A1 (de) 2015-03-10 2016-09-15 Wacker Chemie Ag Verfahren zur Herstellung von pulverförmigen Feststoffen aus Alkalisalzen von Silanolen
WO2016149455A2 (fr) 2015-03-17 2016-09-22 The General Hospital Corporation Interactome arn de complexe répressif polycomb 1 (prc1)
HUE045670T2 (hu) * 2015-04-28 2020-01-28 Evonik Degussa Gmbh Eljárás propén epoxidálására
WO2017184231A1 (fr) * 2016-04-20 2017-10-26 Dow Corning Corporation Composition d'alkylsiliconate de lithium, revêtement et procédé pour les produire
ES2895507T3 (es) * 2016-07-27 2022-02-21 Wacker Chemie Ag Procedimiento para la producción de un ácido silícico de precipitación modificado
JP6786716B2 (ja) 2017-04-04 2020-11-18 ワッカー ケミー アクチエンゲゼルシャフトＷａｃｋｅｒ Ｃｈｅｍｉｅ ＡＧ 反応性シロキサンおよびその製造方法
EP3837305B1 (fr) 2018-08-17 2021-11-03 Wacker Chemie AG Compositions d'organopolysiloxanes réticulables
CN112142772B (zh) * 2020-10-12 2023-07-25 江西晨光新材料股份有限公司 一种烷基硅酸盐的合成方法及其应用

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2438055A (en) 1947-01-10 1948-03-16 Corning Glass Works Preparation of salts of monoorgano silanols
US2567110A (en) 1947-07-12 1951-09-04 Corning Glass Works Organopolysiloxanes prepared by the reaction of salts of silanols with halosilanes
BE520244A (fr) 1952-05-27
NL127074C (fr) 1963-05-31
EP0015366B2 (fr) * 1979-03-05 1990-12-05 Th. Goldschmidt AG Procédé de préparation de solutions aqueuses d'organosiliconates de métaux alcalins
DE4336600C1 (de) 1993-10-27 1994-10-20 Nuenchritz Chemie Gmbh Verfahren zur kontinuierlichen Herstellung wäßriger Alkali-Alkylsiliconatlösungen
DE102008035623A1 (de) * 2008-07-31 2010-02-04 Evonik Degussa Gmbh Verfahren zur Herstellung von Organosilanen
DE102010031624A1 (de) 2010-07-21 2012-01-26 Wacker Chemie Ag Wasserlösliche Organosiliconatpulver

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2013041385A1 *

Also Published As

Publication number Publication date
KR20140054285A (ko) 2014-05-08
CN103827125A (zh) 2014-05-28
DE102011083109A1 (de) 2013-03-21
JP2014530196A (ja) 2014-11-17
WO2013041385A1 (fr) 2013-03-28
US20140228589A1 (en) 2014-08-14

Similar Documents

Publication Publication Date Title
EP2758409A1 (fr) Procédé de production de poudres à base de sels alcalins de silanols
EP2782919B1 (fr) Procédé de production de matières solides à partir de sels alcalins de silanols
EP2596001B1 (fr) Poudres de siliconates organiques solubles dans l'eau
EP0776935B1 (fr) Composés siliciques à bas poids moléculaire, procédé pour leur préparation et leur emploi dans les compositions d'organopolysiloxan réticulables
WO2013127774A1 (fr) Matières réticulables à base de composés organosiliciés
EP2852599A1 (fr) Procédé de production de matières solides à partir de sels alcalins de silanols
EP3164407A1 (fr) Procédé de production de siloxanes à partir de sels alcalins de silanols
US7576169B2 (en) Facile synthesis of polyhedral silsesquioxane anions and use thereof
DE4317978A1 (de) Organosiliciumreste aufweisende Phosphazene, Verfahren zu deren Herstellung und deren Verwendung
DE3518878C2 (fr)
EP0672702B1 (fr) Procédé de préparation d'organopolysiloxanes ayant des groupes de organoxy
WO2015176977A1 (fr) Procédé de préparation de poudres constituées de sels alcalins de silanols par séchage par pulvérisation
EP3221385B1 (fr) Procédé de préparation de siloxanols à partir de sels métalliques de silanols
EP3119788A1 (fr) Procédé de préparation de poudres constituées de sels alcalins de silanols
EP3497149B1 (fr) Siloxanes réactifs et leurs procédés de préparation
EP4175962B1 (fr) Procédé de synthèse d'aminosiloxanes contenant des groupes alcoxy
EP4107210B1 (fr) Silicates d'alkyle
EP3268325A1 (fr) Procédé de fabrication de matières solides pulvérulentes à partir de sels alcalins de silanols

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20140318

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20141009

DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20150220