JPS6334877B2 - - Google Patents
Info
- Publication number
- JPS6334877B2 JPS6334877B2 JP53139470A JP13947078A JPS6334877B2 JP S6334877 B2 JPS6334877 B2 JP S6334877B2 JP 53139470 A JP53139470 A JP 53139470A JP 13947078 A JP13947078 A JP 13947078A JP S6334877 B2 JPS6334877 B2 JP S6334877B2
- Authority
- JP
- Japan
- Prior art keywords
- reaction
- phosphoric acid
- silyl phosphate
- weight
- silyl
- 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.)
- Expired
Links
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 192
- 238000006243 chemical reaction Methods 0.000 claims description 140
- YIKQLNRXIWIZFA-UHFFFAOYSA-N silyl dihydrogen phosphate Chemical compound OP(O)(=O)O[SiH3] YIKQLNRXIWIZFA-UHFFFAOYSA-N 0.000 claims description 126
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 96
- 239000003054 catalyst Substances 0.000 claims description 59
- 238000000034 method Methods 0.000 claims description 39
- 239000011541 reaction mixture Substances 0.000 claims description 38
- 239000000203 mixture Substances 0.000 claims description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 29
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 11
- 230000035484 reaction time Effects 0.000 claims description 8
- 239000007795 chemical reaction product Substances 0.000 claims description 6
- 239000000376 reactant Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 125000000962 organic group Chemical group 0.000 claims description 4
- 150000002430 hydrocarbons Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 238000004821 distillation Methods 0.000 claims description 2
- 125000004437 phosphorous atom Chemical group 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 239000010703 silicon Substances 0.000 claims description 2
- -1 alkyl silicate Chemical compound 0.000 description 70
- 229920001296 polysiloxane Polymers 0.000 description 60
- 229920005645 diorganopolysiloxane polymer Polymers 0.000 description 38
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 25
- 239000000047 product Substances 0.000 description 24
- 229920000642 polymer Polymers 0.000 description 21
- DDJSWKLBKSLAAZ-UHFFFAOYSA-N cyclotetrasiloxane Chemical compound O1[SiH2]O[SiH2]O[SiH2]O[SiH2]1 DDJSWKLBKSLAAZ-UHFFFAOYSA-N 0.000 description 18
- 230000003472 neutralizing effect Effects 0.000 description 15
- 238000006386 neutralization reaction Methods 0.000 description 13
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 11
- 239000002253 acid Substances 0.000 description 10
- 229920002379 silicone rubber Polymers 0.000 description 9
- 150000007513 acids Chemical class 0.000 description 6
- 238000007792 addition Methods 0.000 description 6
- 239000004945 silicone rubber Substances 0.000 description 6
- 230000007062 hydrolysis Effects 0.000 description 5
- 238000006460 hydrolysis reaction Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 238000011067 equilibration Methods 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 3
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 3
- DJHGAFSJWGLOIV-UHFFFAOYSA-N Arsenic acid Chemical compound O[As](O)(O)=O DJHGAFSJWGLOIV-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 229940000488 arsenic acid Drugs 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 150000001923 cyclic compounds Chemical class 0.000 description 2
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 150000004756 silanes Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- IMAYJYGCQCZYID-UHFFFAOYSA-N 1,3,5,7,9,11-hexaoxa-2,4,6,8,10,12-hexasilacyclododecane Chemical class O1[SiH2]O[SiH2]O[SiH2]O[SiH2]O[SiH2]O[SiH2]1 IMAYJYGCQCZYID-UHFFFAOYSA-N 0.000 description 1
- CCPYCNSBZPTUMJ-UHFFFAOYSA-N 1,3,5,7,9,2,4,6,8,10-pentaoxapentasilecane Chemical class O1[SiH2]O[SiH2]O[SiH2]O[SiH2]O[SiH2]1 CCPYCNSBZPTUMJ-UHFFFAOYSA-N 0.000 description 1
- MFGOFGRYDNHJTA-UHFFFAOYSA-N 2-amino-1-(2-fluorophenyl)ethanol Chemical compound NCC(O)C1=CC=CC=C1F MFGOFGRYDNHJTA-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 206010001488 Aggression Diseases 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- HUCVOHYBFXVBRW-UHFFFAOYSA-M caesium hydroxide Inorganic materials [OH-].[Cs+] HUCVOHYBFXVBRW-UHFFFAOYSA-M 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 150000008282 halocarbons Chemical group 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000010406 interfacial reaction Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920006120 non-fluorinated polymer Polymers 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 1
- 125000005375 organosiloxane group Chemical group 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000548 poly(silane) polymer Polymers 0.000 description 1
- 238000012667 polymer degradation Methods 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 150000007521 triprotic acids Chemical class 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/095—Compounds containing the structure P(=O)-O-acyl, P(=O)-O-heteroatom, P(=O)-O-CN
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
- B01J31/123—Organometallic polymers, e.g. comprising C-Si bonds in the main chain or in subunits grafted to the main chain
- B01J31/124—Silicones or siloxanes or comprising such units
- B01J31/125—Cyclic siloxanes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Silicon Polymers (AREA)
- Catalysts (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/877,053 US4125551A (en) | 1978-02-13 | 1978-02-13 | Process for producing silylphosphates |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54109924A JPS54109924A (en) | 1979-08-29 |
| JPS6334877B2 true JPS6334877B2 (en, 2012) | 1988-07-12 |
Family
ID=25369153
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13947078A Granted JPS54109924A (en) | 1978-02-13 | 1978-11-14 | Manufacture of silylphosphate |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4125551A (en, 2012) |
| JP (1) | JPS54109924A (en, 2012) |
| DE (1) | DE2849108A1 (en, 2012) |
| FR (1) | FR2416898A1 (en, 2012) |
| GB (1) | GB2016492B (en, 2012) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4977289A (en) * | 1987-11-25 | 1990-12-11 | General Electric Company | Catalyst for producing fluorosilicone polymers |
| US4897459A (en) * | 1987-11-25 | 1990-01-30 | General Electric Company | Catalyst for producing fluorosilicone polymers |
| JPH0733505B2 (ja) * | 1989-02-28 | 1995-04-12 | 信越化学工業株式会社 | 撥水処理剤 |
| US5041586A (en) * | 1990-11-29 | 1991-08-20 | Dow Corning Corporation | Method of preparing a silyphosphate mixture, silyphosphate mixture and its use in stabilizing metal silanolates in siloxane polymers |
| CA2103362C (en) * | 1991-06-05 | 2002-04-16 | Achilles Chiotis | Flame retarded gel compositions |
| US5099051A (en) * | 1991-08-16 | 1992-03-24 | Dow Corning Corporation | Siloxanyl-phosphate mixture and its use in stabilizing metal silanolates in siloxane polymers |
| US5922816A (en) * | 1992-06-02 | 1999-07-13 | General Electric Company | Polyester-polycarbonate compositions stabilized against ester-carbonate interchange |
| DE4323183C2 (de) * | 1993-07-10 | 1996-06-05 | Huels Silicone Gmbh | Verfahren zur Herstellung von Silylphosphaten und Siloxanylphosphaten und deren Verwendung |
| JPH07216091A (ja) * | 1994-01-27 | 1995-08-15 | Toray Dow Corning Silicone Co Ltd | シロキサニル・ホスフェートの製造方法 |
| US5710300A (en) * | 1997-04-11 | 1998-01-20 | Dow Corning Corporation | Siloxy phosphonate as stabilizing agent for polydiorganosiloxanes |
| FR2845089B1 (fr) * | 2002-10-01 | 2004-12-10 | Rhodia Chimie Sa | Phosphates de silanoxyle, leur preparation et leur utilisation dans la synthese de polyorganosiloxanes lineaires |
| US8921503B2 (en) * | 2011-03-31 | 2014-12-30 | Akzo Nobel Coatings International B.V. | Foul preventing coating composition |
| DE102014206359A1 (de) * | 2014-04-03 | 2015-10-08 | Evonik Degussa Gmbh | VOC-arme Dialkyl-funktionelle Alkoxysiloxane, Verfahren und deren Verwendung als hydrophobierende Imprägniermittel für mineralische Baustoffe |
| US9868902B2 (en) | 2014-07-17 | 2018-01-16 | Soulbrain Co., Ltd. | Composition for etching |
| JP6580397B2 (ja) * | 2014-07-17 | 2019-09-25 | ソウルブレイン シーオー．， エルティーディー． | エッチング用組成物及びこれを用いた半導体素子の製造方法 |
| CN109503653B (zh) * | 2018-12-25 | 2021-08-24 | 苏州祺添新材料有限公司 | 一种三(三烃基硅基)磷酸酯的合成方法 |
| CN111349243A (zh) * | 2020-04-13 | 2020-06-30 | 新纳奇材料科技江苏有限公司 | 一种单端烷氧基单端乙烯基聚二甲基硅氧烷的制备方法 |
| CN111378135A (zh) * | 2020-04-30 | 2020-07-07 | 新纳奇材料科技江苏有限公司 | 一种低粘度烷氧基封端聚二甲基硅氧烷的制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2951860A (en) * | 1957-11-15 | 1960-09-06 | Dow Corning | Organosilicon hydroxy phosphate esters |
| US3441537A (en) * | 1967-07-12 | 1969-04-29 | Stauffer Chemical Co | Organopolysiloxanes |
| US4008261A (en) * | 1975-01-02 | 1977-02-15 | Dow Corning Corporation | Method of preparing phosphonium siloxanes and products thereof |
-
1978
- 1978-02-13 US US05/877,053 patent/US4125551A/en not_active Expired - Lifetime
- 1978-11-07 GB GB7843464A patent/GB2016492B/en not_active Expired
- 1978-11-11 DE DE19782849108 patent/DE2849108A1/de not_active Withdrawn
- 1978-11-14 JP JP13947078A patent/JPS54109924A/ja active Granted
-
1979
- 1979-02-13 FR FR7903598A patent/FR2416898A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| US4125551A (en) | 1978-11-14 |
| GB2016492A (en) | 1979-09-26 |
| JPS54109924A (en) | 1979-08-29 |
| DE2849108A1 (de) | 1979-08-23 |
| FR2416898B1 (en, 2012) | 1984-06-15 |
| FR2416898A1 (fr) | 1979-09-07 |
| GB2016492B (en) | 1982-10-13 |
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