GB711374A - Improvements in and relating to methods for improving the adhesion of organopolysiloxanes to solid surfaces - Google Patents
Improvements in and relating to methods for improving the adhesion of organopolysiloxanes to solid surfacesInfo
- Publication number
- GB711374A GB711374A GB23473/51A GB2347351A GB711374A GB 711374 A GB711374 A GB 711374A GB 23473/51 A GB23473/51 A GB 23473/51A GB 2347351 A GB2347351 A GB 2347351A GB 711374 A GB711374 A GB 711374A
- Authority
- GB
- United Kingdom
- Prior art keywords
- coating
- group
- organopolysiloxane
- butoxytriethoxysilane
- silicate
- 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
- 229920001296 polysiloxane Polymers 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 2
- 239000007787 solid Substances 0.000 title abstract 2
- 239000011248 coating agent Substances 0.000 abstract 6
- 238000000576 coating method Methods 0.000 abstract 6
- -1 isooctyl decyl Chemical group 0.000 abstract 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 abstract 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- RJMRIDVWCWSWFR-UHFFFAOYSA-N methyl(tripropoxy)silane Chemical compound CCCO[Si](C)(OCCC)OCCC RJMRIDVWCWSWFR-UHFFFAOYSA-N 0.000 abstract 2
- HWEIUHIKNYRKGA-UHFFFAOYSA-N tert-butyl triethyl silicate Chemical compound CCO[Si](OCC)(OCC)OC(C)(C)C HWEIUHIKNYRKGA-UHFFFAOYSA-N 0.000 abstract 2
- NJHMXNLHQBCHNJ-UHFFFAOYSA-N 2-chloroethoxy(trihydroxy)silane Chemical compound C(CCl)O[Si](O)(O)O NJHMXNLHQBCHNJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004342 Benzoyl peroxide Substances 0.000 abstract 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- 239000005046 Chlorosilane Substances 0.000 abstract 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 abstract 1
- 239000004965 Silica aerogel Substances 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 1
- 229910008046 SnC14 Inorganic materials 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
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000002877 alkyl aryl 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
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 235000019400 benzoyl peroxide Nutrition 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
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- ROQBUFODTIIROY-UHFFFAOYSA-N butyl triethyl silicate Chemical compound CCCCO[Si](OCC)(OCC)OCC ROQBUFODTIIROY-UHFFFAOYSA-N 0.000 abstract 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical class Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 abstract 1
- PQXURBRJSIVVTH-UHFFFAOYSA-N dibutyl diethyl silicate Chemical compound CCCCO[Si](OCC)(OCC)OCCCC PQXURBRJSIVVTH-UHFFFAOYSA-N 0.000 abstract 1
- GQUUKQQWGMHLQK-UHFFFAOYSA-N ditert-butyl diethyl silicate Chemical compound CCO[Si](OCC)(OC(C)(C)C)OC(C)(C)C GQUUKQQWGMHLQK-UHFFFAOYSA-N 0.000 abstract 1
- FYIPWZRORZGZGS-UHFFFAOYSA-N ditert-butyl diphenyl silicate Chemical compound C=1C=CC=CC=1O[Si](OC(C)(C)C)(OC(C)(C)C)OC1=CC=CC=C1 FYIPWZRORZGZGS-UHFFFAOYSA-N 0.000 abstract 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 239000003517 fume Substances 0.000 abstract 1
- 229910052736 halogen Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- HLXDKGBELJJMHR-UHFFFAOYSA-N methyl-tri(propan-2-yloxy)silane Chemical compound CC(C)O[Si](C)(OC(C)C)OC(C)C HLXDKGBELJJMHR-UHFFFAOYSA-N 0.000 abstract 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 150000001282 organosilanes Chemical class 0.000 abstract 1
- 125000005375 organosiloxane group Chemical group 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 abstract 1
- 239000004408 titanium dioxide Substances 0.000 abstract 1
- 125000003944 tolyl group Chemical group 0.000 abstract 1
- GYZQBXUDWTVJDF-UHFFFAOYSA-N tributoxy(methyl)silane Chemical compound CCCCO[Si](C)(OCCCC)OCCCC GYZQBXUDWTVJDF-UHFFFAOYSA-N 0.000 abstract 1
- YSOYYQBKBBPTED-UHFFFAOYSA-N triethyl 2-methylbutan-2-yl silicate Chemical compound C(C)(C)(CC)O[Si](OCC)(OCC)OCC YSOYYQBKBBPTED-UHFFFAOYSA-N 0.000 abstract 1
- ZEOPCIFVJGABLT-UHFFFAOYSA-N trihydroxy(2-methoxyethoxy)silane Chemical compound COCCO[Si](O)(O)O ZEOPCIFVJGABLT-UHFFFAOYSA-N 0.000 abstract 1
- 125000005023 xylyl group Chemical group 0.000 abstract 1
- 239000011787 zinc oxide Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/24—Coatings containing organic materials
- C03C25/40—Organo-silicon compounds
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US711374XA | 1950-10-14 | 1950-10-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB711374A true GB711374A (en) | 1954-06-30 |
Family
ID=22099472
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB23473/51A Expired GB711374A (en) | 1950-10-14 | 1951-10-09 | Improvements in and relating to methods for improving the adhesion of organopolysiloxanes to solid surfaces |
Country Status (2)
| Country | Link |
|---|---|
| BE (1) | BE506400A (enrdf_load_stackoverflow) |
| GB (1) | GB711374A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4215165A (en) * | 1978-07-17 | 1980-07-29 | Chemische Werke Huls Aktiengesellschaft | Method for coating of glass surfaces |
| US4268554A (en) * | 1977-10-13 | 1981-05-19 | Rainer Gras | Process for the coating of glass surfaces |
| US4828588A (en) * | 1988-04-01 | 1989-05-09 | University Of Cincinnati | Process for preparation of heterogeneous polysiloxane membrane and membrane produced |
-
0
- BE BE506400D patent/BE506400A/xx unknown
-
1951
- 1951-10-09 GB GB23473/51A patent/GB711374A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4268554A (en) * | 1977-10-13 | 1981-05-19 | Rainer Gras | Process for the coating of glass surfaces |
| US4215165A (en) * | 1978-07-17 | 1980-07-29 | Chemische Werke Huls Aktiengesellschaft | Method for coating of glass surfaces |
| US4828588A (en) * | 1988-04-01 | 1989-05-09 | University Of Cincinnati | Process for preparation of heterogeneous polysiloxane membrane and membrane produced |
Also Published As
| Publication number | Publication date |
|---|---|
| BE506400A (enrdf_load_stackoverflow) |
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