GB960240A - New silicon compounds - Google Patents
New silicon compoundsInfo
- Publication number
- GB960240A GB960240A GB42558/61A GB4255861A GB960240A GB 960240 A GB960240 A GB 960240A GB 42558/61 A GB42558/61 A GB 42558/61A GB 4255861 A GB4255861 A GB 4255861A GB 960240 A GB960240 A GB 960240A
- Authority
- GB
- United Kingdom
- Prior art keywords
- weight
- preparation
- examples
- specified
- oc3h6
- 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
- 150000003377 silicon compounds Chemical class 0.000 title 1
- 229920000642 polymer Polymers 0.000 abstract 5
- -1 alkoxy silanes Chemical class 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 238000002360 preparation method Methods 0.000 abstract 4
- 229920005830 Polyurethane Foam Polymers 0.000 abstract 3
- 150000001298 alcohols Chemical class 0.000 abstract 3
- 238000009835 boiling Methods 0.000 abstract 3
- 239000011496 polyurethane foam Substances 0.000 abstract 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 2
- 229920001400 block copolymer Polymers 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000005702 oxyalkylene group Chemical group 0.000 abstract 2
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 abstract 1
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 239000005046 Chlorosilane Substances 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005639 Lauric acid Substances 0.000 abstract 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001335 aliphatic alkanes Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 239000011230 binding agent Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 150000001896 cresols Chemical class 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 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 abstract 1
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 1
- 239000012948 isocyanate Substances 0.000 abstract 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 abstract 1
- 150000002513 isocyanates Chemical class 0.000 abstract 1
- JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical compound C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 abstract 1
- 229920000570 polyether Polymers 0.000 abstract 1
- 229920001228 polyisocyanate Polymers 0.000 abstract 1
- 239000005056 polyisocyanate Substances 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 229920005604 random copolymer Polymers 0.000 abstract 1
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 abstract 1
- 229910000077 silane Inorganic materials 0.000 abstract 1
- 150000004756 silanes Chemical class 0.000 abstract 1
- 239000000377 silicon dioxide Substances 0.000 abstract 1
- 229920002545 silicone oil Polymers 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 125000003944 tolyl group Chemical group 0.000 abstract 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 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
- 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
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
-
- 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
- C07F7/04—Esters of silicic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
The invention comprises alkoxy silanes of the general formula: Ry Si[(OCnH2n)a (OCmH2m)bX]4-y wherein R is a hydrocarbon radical optionally substituted with chlorine, X is a monovalent radical derived from a compound XH in which H is a hydrogen atom reactive with a cyclic oxide, y is 0, 1 or 2; n is 2, 3 or 4, m is 3 or 4, a is 0 or an integer and b is greater than 4, which are used in the preparation of polyurethane foams. The silanes may be prepared by reacting silica tetrachloride or an appropriate chloro-silane with (a) monohydric alcohols of general formula H(OCnH2n)a (OCmH2m)bX wherei X, a, b, n and m have the values above, in presence of pyridine and acid binding agent, (b) the sodium salt of the above monohydric alcohols, or (c) by ester interchange, e.g. between tetraethoxy silane and a monohydric alcohol as defined above. Specified starting materials are CH3SiCl3, (CH3)2SiCl2; CH3Si(OC2H5)3, (CH3)2Si(OC2H5)2, C6H5SiCl3 and C6H5C2 H4Si(OC2H5)3. R may be straight or branched chain alkyl, cycloalkyl, aryl or aralkyl, substituted or unsubstituted, the same or different and among those specified are methyl, iso-butyl, cyclohexyl, benzyl and tolyl. The compounds XH used to obtain radical X include monohydric aliphatic, cycloaliphatic and arylaliphatic alcohols, phenols, secondary amines, carboxylic acids or mono N-substituted carboxylic amides. Many are specified and include isooctanol, cresols, N:N dialkylethanolamines, N alkyl acetamides, butyric acid and lauric acid. When a above is an integer the copolymers may be random or block copolymers, the oxyalkylene residue of molecular weight of 250 to 3,000 containing at least 50% of oxyalkylene units containing at least 3 carbon atoms per unit. Polyurethane foams are prepared by reacting organic polyisocyanates and hydroxyl group containing polymers having at least two hydroxyl groups per molecule in the presence of water preferably 1% to 10% by weight of the hydroxylic polymer and/or a low boiling liquid, said process being carried out in presence of an alkoxyl silane as define above. Hydroxyl group containing polymers specified are polyesters and polyesteramides having molecular weights of 200 to 5,000 and polyethers having molecular weights of 200 to 8,000 containing at least two isocyanate reactive groups. Many examples are given along with their methods of preparation. Low boiling point liquids used in amounts of 1% to 100% by weight based on the hydroxylic polymer are inert towards isocyanates and have boiling points less than 75 DEG C., e.g. fluorinated alkanes. The alcoxysilane is incorporated in amounts of from 0.1% to 5.0% by weight of the hydroxy group containing polymer, and in addition, 0.01% to 2.5% by weight of a block copolymer (MW. 1,000 to 10,000) or a silicone oil may also be added. Examples 1 to 3 describe the preparation of: Si [(OC3H6)8.6 OC8H17]4; CH3Si[(OC3H6)14.1 O.C8H17]3 and CH3Si[(OC2H4)15.5 (OC3H6)11.7OC8H17]3 and Examples 4 to 9 the preparation of polyurethane foams in presence of the products of Examples 1 to 3.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB42558/61A GB960240A (en) | 1961-11-28 | 1961-11-28 | New silicon compounds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB42558/61A GB960240A (en) | 1961-11-28 | 1961-11-28 | New silicon compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB960240A true GB960240A (en) | 1964-06-10 |
Family
ID=10424952
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB42558/61A Expired GB960240A (en) | 1961-11-28 | 1961-11-28 | New silicon compounds |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB960240A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1694366B1 (en) * | 1968-03-16 | 1970-11-12 | Goldschmidt Ag Th | Process for the production of polyurethane foams from polyethers |
| USRE30698E (en) | 1973-01-10 | 1981-08-04 | Castrol Limited | Hydraulic fluids comprising orthosilicate esters |
| EP0162588A1 (en) * | 1984-04-24 | 1985-11-27 | Polyol International B.V. | Preparation of polymer polyols |
-
1961
- 1961-11-28 GB GB42558/61A patent/GB960240A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1694366B1 (en) * | 1968-03-16 | 1970-11-12 | Goldschmidt Ag Th | Process for the production of polyurethane foams from polyethers |
| USRE30698E (en) | 1973-01-10 | 1981-08-04 | Castrol Limited | Hydraulic fluids comprising orthosilicate esters |
| EP0162588A1 (en) * | 1984-04-24 | 1985-11-27 | Polyol International B.V. | Preparation of polymer polyols |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3161614A (en) | Polyfunctional alkoxy endblocked polysiloxanes and their cured compositions | |
| US2846458A (en) | Organosiloxane ethers | |
| US4749766A (en) | Organotin curing catalyst for vulcanizable organopolysiloxanes | |
| US3364160A (en) | Organo-polysiloxane composition convertible at room temperature | |
| US2834748A (en) | Siloxane-oxyalkylene block copolymers | |
| US4554369A (en) | Organosilicon compounds and preparation and use thereof | |
| GB971682A (en) | Polysiloxane isocyanates | |
| US4552942A (en) | Silanes and compositions prepared therefrom | |
| US4020044A (en) | Method of increasing the molecular weight of hydroxyl endblocked polydiorganosiloxanes | |
| GB1265098A (en) | ||
| GB1095928A (en) | Aminoxy-substituted silicon materials | |
| CA1253655A (en) | Stabilized blends of thiofunctional polysiloxane fluids and organopolysiloxane fluids and a process for stabilizing the same | |
| US3338943A (en) | Aminoorganosiloxane-carboxyorganosiloxane copolymers | |
| US2721855A (en) | Air-drying organosilicon compositions containing a titanic acid ester | |
| US4230816A (en) | Thiofunctional polysiloxane polymers | |
| US3455980A (en) | Pentacoordinate silicon complexes of vicinal aliphatic diols | |
| US5786493A (en) | Cyclic silane esters and solvolysis products thereof, and processes for the preparation of the cyclic silane esters and the solvolysis products | |
| US3170941A (en) | Nitrogen-containing spiranes and siloxanes and their preparation | |
| GB960240A (en) | New silicon compounds | |
| US4633002A (en) | Aminofunctional polysiloxane compounds and method of preparation therefor | |
| US3278485A (en) | Non-ionic organopolysiloxanes | |
| GB998992A (en) | Improvements in or relating to organosilicon compositions | |
| US3271360A (en) | Polymeric organosiloxanes | |
| GB1066550A (en) | Process for the manufacture of polyorganosiloxane elastomers | |
| US3287291A (en) | Diorganosiloxanes cured with an alkoxy end-blocked silyl tetraformal |