GB795894A - Alkoxysilylpropylamines - Google Patents
AlkoxysilylpropylaminesInfo
- Publication number
- GB795894A GB795894A GB135756A GB135756A GB795894A GB 795894 A GB795894 A GB 795894A GB 135756 A GB135756 A GB 135756A GB 135756 A GB135756 A GB 135756A GB 795894 A GB795894 A GB 795894A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mono
- mols
- ammonia
- water
- amine
- 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
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 9
- -1 siloxanes Chemical class 0.000 abstract 5
- 229910021529 ammonia Inorganic materials 0.000 abstract 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000003365 glass fiber Substances 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 239000000463 material Substances 0.000 abstract 2
- 229920001296 polysiloxane Polymers 0.000 abstract 2
- 239000000376 reactant Substances 0.000 abstract 2
- 229910000077 silane Inorganic materials 0.000 abstract 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 abstract 1
- KSCAZPYHLGGNPZ-UHFFFAOYSA-N 3-chloropropyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)CCCCl KSCAZPYHLGGNPZ-UHFFFAOYSA-N 0.000 abstract 1
- MWZXHAXMAVEYGN-UHFFFAOYSA-N 3-triethoxysilyl-n,n-bis(3-triethoxysilylpropyl)propan-1-amine Chemical class CCO[Si](OCC)(OCC)CCCN(CCC[Si](OCC)(OCC)OCC)CCC[Si](OCC)(OCC)OCC MWZXHAXMAVEYGN-UHFFFAOYSA-N 0.000 abstract 1
- 239000000539 dimer Substances 0.000 abstract 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 239000002990 reinforced plastic Substances 0.000 abstract 1
- 150000004756 silanes Chemical class 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Silicon Polymers (AREA)
Abstract
Fibrous glass material is sized or finished by applying thereto a solution obtained by adding an alkoxysilylpropylamine having the formula: <FORM:0795894/IV (b)/1> where R is an alkly group, R1 is a hydrogen atom or an alkyl or aryl group, and x and y are each 0, 1 or 2, to water or to aqueous organic mixtures. In solution, the silanes are converted to aminopropylpolysiloxanes. The treated glass fibres are particularly useful for the preparation of reinforced plastics, e.g. laminates.ALSO:The invention comprises alkoxysilylpropylamines of the formula <FORM:0795894/IV (a)/1> where R is an alkyl group, R1 is a hydrogen atom or an alkyl or aryl group, and x and y are each 0, 1 or 2. They are prepared by reacting ammonia with a gamma-chloropropylalkoxysilane at a temperature of at least 90 DEG C. and at superatmospheric pressure. The products are mixtures of mono-, bis- and tris-amines, the proportion of monoamine being greater with greater mol. fractions of ammonia in the reactants. The proportion of reactants may vary from about 1 to 20 mols. of ammonia per mol. of silane. The compounds are hydrolysable to siloxanes which form clear, stable solutions in water or in aqueous organic mixtures which are useful as sizes for fibrous glass material. The compounds may also be reacted with compounds containing methylol groups and the products subsequently hydrolysed. In the examples: (1) gamma - chloropropyltriethoxy silane (0.3 mols.) is heated with ammonia (3.0 mols.) at 100 DEG C. under autogenous pressure, and a fraction of the product is identified as mono-(triethoxysilylpropyl)amine; (2) the mono-, bis-and tris-(triethoxysilylpropyl)amines are identified after a similar reaction as in (1); (3) 50 per cent yield of the mono-amine is obtained using 20 mols. of liquid ammonia per mol. of silane; (4) the mono-amine is hydrolysed in water and the polysiloxane is obtained in glassy and in powder form, both of which form clear solutions in water. The Specification also discloses an aminopropylmethyl polysiloxane and a dimer of aminopropyldialkyl siloxane.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB135756A GB795894A (en) | 1956-01-16 | 1956-01-16 | Alkoxysilylpropylamines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB135756A GB795894A (en) | 1956-01-16 | 1956-01-16 | Alkoxysilylpropylamines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB795894A true GB795894A (en) | 1958-06-04 |
Family
ID=22151494
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB135756A Expired GB795894A (en) | 1956-01-16 | 1956-01-16 | Alkoxysilylpropylamines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB795894A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4374237A (en) | 1981-12-21 | 1983-02-15 | Union Carbide Corporation | Silane-containing isocyanate-terminated polyurethane polymers |
-
1956
- 1956-01-16 GB GB135756A patent/GB795894A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4374237A (en) | 1981-12-21 | 1983-02-15 | Union Carbide Corporation | Silane-containing isocyanate-terminated polyurethane polymers |
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