GB740573A - Improvements in or relating to organopolysiloxane adhesive compositions and adhesive tapes - Google Patents

Improvements in or relating to organopolysiloxane adhesive compositions and adhesive tapes

Info

Publication number
GB740573A
GB740573A GB16900/53A GB1690053A GB740573A GB 740573 A GB740573 A GB 740573A GB 16900/53 A GB16900/53 A GB 16900/53A GB 1690053 A GB1690053 A GB 1690053A GB 740573 A GB740573 A GB 740573A
Authority
GB
United Kingdom
Prior art keywords
per cent
grams
composition
resin
sio2
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
Application number
GB16900/53A
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.)
Midland Silicones Ltd
Original Assignee
Midland Silicones Ltd
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 Midland Silicones Ltd filed Critical Midland Silicones Ltd
Publication of GB740573A publication Critical patent/GB740573A/en
Expired legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/46Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes silicones
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38Pressure-sensitive adhesives [PSA]
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04Polysiloxanes

Abstract

An adhesive composition suitable inter alia for making pressure-sensitive tapes (see Group VIII), comprises a mixture of (a) 5 to 70 per cent by weight of a benzene-soluble copolymer resin consisting of SiO2 and R3SiO 1/2 units and from 0 to 0.2 R2SiO units per SiO2 unit, R being alkyl up to three carbon atoms or phenyl and at least 90 per cent of the R radicals being alkyl, and the ratio of R3SiO 1/2 plus R2SiO units to SiO2 units being from 0.6 : 1 to 0.9 : 1, and (b) 95 to 30 per cent of a benzene soluble organosiloxane having a viscosity of at least one million cs. and having the formula Rl2SiO where R1 is methyl or phenyl and at least 90 per cent of the R1 radicals are methyl. The composition may also contain up to 10 per cent by weight of a titanium orthoester or a hydrocarbon-soluble partial hydrolysate thereof, the organic radicals in the ester being aliphatic or hydroxylated aliphatic having less than 20 carbon atoms. The copolymers (a) may be made by the co-hydrolysis of the appropriate chloro- or alkoxy-silanes in the presence of a water-miscible solvent, but are preferably prepared by the process of Specification 706,719. The compositions may contain curing catalysts such as alkyl zirconates and borates, metal alkoxides, metal salts of carboxylic acids and alkoxy silanes such as ethyl silicate, and fillers, e.g. ferric oxide, titanium dioxide and zinc oxide, up to 3 per cent of the composition. The compositions are prepared by mixing the ingredients alone or in a common solvent such as an aromatic or petroleum hydrocarbon solvent. After coating any suitable surface with the composition the composition is cured by air drying or heating at temperatures up to 300 DEG C. The adhesives will adhere to practically any solid surface including fluorocarbon polymers and polyethylene. A typical copolymer (a) was prepared as follows:-450 grams of isopropanol was added to a solution of 432 grams sodium silicate in 864 grams water acidified with 252 grams concentrated hydrochloric acid, followed by 222 grams trimethylchlorosilane and 288 grams hexamethylsiloxane, and the mixture refluxed for half-an-hour. The resulting resin was separated as a toluene solution. The resin had a (CH3)3Si:SiO2 ratio of 0.8. In examples 1, 2, 4 and 5 compositions containing various quantities of resin (a) prepared as above and a high molecular weight dimethylpolysiloxane or phenyl methylpolysiloxane dissolved in a petroleum hydrocarbon solvent were applied to glass tapes. The adhesive strengths were tested either after removing the solvent by air drying or by drying at 250 DEG C. for 5 minutes. In example 4, 2 per cent (of the total polymer weight) of various titanium esters were added. In example 5 various curing catalysts were employed with heat treatment at 150 DEG or 250 DEG C. for five minutes. In example 6 various other backings for adhesive tapes were employed. In example 7 a different resin (a) was employed.
GB16900/53A 1952-07-02 1953-06-18 Improvements in or relating to organopolysiloxane adhesive compositions and adhesive tapes Expired GB740573A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US740573XA 1952-07-02 1952-07-02

Publications (1)

Publication Number Publication Date
GB740573A true GB740573A (en) 1955-11-16

Family

ID=22117434

Family Applications (1)

Application Number Title Priority Date Filing Date
GB16900/53A Expired GB740573A (en) 1952-07-02 1953-06-18 Improvements in or relating to organopolysiloxane adhesive compositions and adhesive tapes

Country Status (2)

Country Link
DE (1) DE941090C (en)
GB (1) GB740573A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1035824B (en) * 1956-10-29 1958-08-07 Licentia Gmbh Use of a silicone resin mixture for the connection of flexible mica laminates
DE970125C (en) * 1956-01-08 1958-08-21 Wacker Chemie Gmbh Bonding of silicone rubber with other materials under pressure and heat
US2979479A (en) * 1957-07-15 1961-04-11 Gen Electric Silicone rubber of improved tear strength
US2999078A (en) * 1961-09-05 Organosiloxane coating composition of
US3176364A (en) * 1959-10-06 1965-04-06 Dritz Arthur Separable fastener

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1074180B (en) * 1960-01-28 Pirmasens Edmund Schneider (Pfalz) Adhesive made from natural or synthetic rubber based on polydiene
CA589294A (en) * 1955-07-13 1959-12-22 L. Marshall Walter Adhesive silicone rubber sheet material and tapes and method of preparing the same
DE1030488B (en) * 1956-04-13 1958-05-22 Patricia Bjerregaard Lavanchy Primer for anchoring customary sticky and pressure-sensitive adhesives on, in particular, hydrophilic substrates, especially for customary adhesive films, adhesive strips and the like. like
DE1263887B (en) * 1957-01-22 1968-03-21 Westinghouse Electric Corp Use of a thermosetting organopolysiloxane resin composition as an adhesive composition in electrical engineering
DE1063228B (en) * 1957-02-11 1959-08-13 Helmut Jedlicka Process for the production of electrical and electronic devices with printed circuits
BE577335A (en) * 1958-04-03
DE1099675B (en) * 1959-04-09 1961-02-16 Guy Joseph Crocker Pressure-sensitive adhesive based on a mixture of a polymer with a tackifying resin
DE1283421B (en) * 1960-03-14 1968-11-21 Wacker Chemie Gmbh Production of protective and insulating coatings on glass, ceramic and plastic vessels, pipes and devices
BR8008995A (en) * 1980-01-28 1981-11-03 Dow Corning SILICON ADHESIVE FORMULATIONS

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE837173C (en) * 1947-03-10 1952-04-21 Rhone Poulenc Sa Process for the production of new water-repellent silicon compounds

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2999078A (en) * 1961-09-05 Organosiloxane coating composition of
DE970125C (en) * 1956-01-08 1958-08-21 Wacker Chemie Gmbh Bonding of silicone rubber with other materials under pressure and heat
DE1035824B (en) * 1956-10-29 1958-08-07 Licentia Gmbh Use of a silicone resin mixture for the connection of flexible mica laminates
US2979479A (en) * 1957-07-15 1961-04-11 Gen Electric Silicone rubber of improved tear strength
US3176364A (en) * 1959-10-06 1965-04-06 Dritz Arthur Separable fastener

Also Published As

Publication number Publication date
DE941090C (en) 1956-04-05

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