SE7401593L - - Google Patents

Info

Publication number
SE7401593L
SE7401593L SE7401593A SE7401593A SE7401593L SE 7401593 L SE7401593 L SE 7401593L SE 7401593 A SE7401593 A SE 7401593A SE 7401593 A SE7401593 A SE 7401593A SE 7401593 L SE7401593 L SE 7401593L
Authority
SE
Sweden
Prior art keywords
siloxane
carbon atoms
formula
composition
vinyl
Prior art date
Application number
SE7401593A
Other versions
SE408619B (en
Inventor
G A L Gant
Original Assignee
Dow Corning
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 Dow Corning filed Critical Dow Corning
Publication of SE7401593L publication Critical patent/SE7401593L/xx
Publication of SE408619B publication Critical patent/SE408619B/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D5/00Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
    • B05D5/08Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain an anti-friction or anti-adhesive surface
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D3/00Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
    • B05D3/06Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation
    • B05D3/061Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation using U.V.
    • B05D3/065After-treatment
    • B05D3/067Curing or cross-linking the coating

Abstract

1433461 Vinyl-containing siloxane polymers cured by ultra-violet radiation DOW CORNING CORP 7 Feb 1974 [28 Sept 1973] 05610/74 Headings C3P and C3T [Also in Division B2] The release of adhesive materials from a solid substrate is improved by applying to the substrate a composition comprising (A) a siloxane consisting essentially of 0À5-100 mole per cent of vinyl-containing siloxane units of formula wherein R is a monovalent hydrocarbon or monovalent halogenated hydrocarbon radical which contains 1-30 carbon atoms and n is 0, 1 or 2, any non-vinyl-containing siloxane units present having the formula wherein R<SP>1</SP> is as defined for R and m is 0-3, (B) a siloxane containing at least one siliconbonded hydrogen atom per molecule, the ratio of silicon-bonded vinyl groups in (A) to the silicon-bonded hydrogen groups in (B) being in the range of 1 : 100 to 100 : 1, and (C) a photo- , sensitizer (preferably 0À1-20% by weight), and curing said composition by exposure to ultraviolet light of wavelength less than 3650 Š. R and R<SP>1</SP> are preferably selected from methyl, ethyl, phenyl, chloropropyl and 3,3,3-trifluoropropyl radicals with n and m having average values of about 1 and 2 respectively. Especially preferred (A) is one which is composed of 100 mole per cent of the vinyl-containing siloxane units. Siloxane (B) may have the general formula wherein a is 0-99 (especially 0), b is 1-100, the sum of a and b being 1-100. A preferred composition is (A) a siloxane of vinylmethylsiloxane units and dimethylsiloxane units end-blocked with trimethylsiloxy units or vinyldimethylsiloxy units and (B) a siloxane of general formula wherein b is 1-100. The composition may also contain a mercapto-functional silicone (D) which comprises any silane or siloxane containing at least one mercapto group (HS-) attached to a silicon atom through one or more carbon atoms, which accelerates the cure of the composition. The silane (D) is of formula wherein R<SP>3</SP> is a divalent (p is 1) or trivalent (p is 2) hydrocarbon radical of 1-18 carbon atoms, one bond of which is attached to the silicon atom and the other bonds attached to the mercapto group, q is 1 or 2, R<SP>4</SP> is a monovalent hydrocarbon radical of 1-30 carbon atoms, s is 0-3, and X is a hydrolysable group, the sum of q and s being 1-4. A preferred silane is one in which R<SP>3</SP> is propylene, p is 1, q is 1, s is 0, and X is a methoxy group. The siloxane (D) is of formula wherein R<SP>3</SP> and R<SP>4</SP> are defined as above, v is 0-2, p and q are defined as above, the sum of q and v being 1-3, any other siloxane units present having the general formula wherein Q is a monovalent hydrocarbon or monovalent halogenated hydrocarbon radical of 1-30 carbon atoms, and t is 0-3. A preferred siloxane is one in which R<SP>3</SP> is a propylene radical, p, q and v are 1, R<SP>4</SP> and Q are methyl radicals, and t is 3. The invention also includes a composition for treating a solid substrate to improve its release characteristics, said composition comprising (1) a siloxane consisting essentially of 0À1-100 mole per cent of mercaptofunctional containing siloxane units having the formula wherein R<SP>2</SP> is an alkylene radical, y is 1 or 2, R<SP>5</SP> is a monovalent hydrocarbon or monovalent halogenated hydrocarbon radical of 1-30 carbon atoms, x is 0-2, and the sum of x and y is 1-3, any non-mercapto functional siloxane units present having the formula wherein R<SP>4</SP> is a monovalent hydrocarbon or monovalent halogenated hydrocarbon radical of 1-30 carbon atoms and z is 0-3, and (2) a siloxane consisting essentially of 0À1-100 mole per cent of vinyl-containing siloxane units of formula wherein R is a monovalent hydrocarbon or a monovalent halogenated hydrocarbon radical of 1-30 carbon atoms and n is 0-2, any non- vinyl containing siloxane units present in (2) having the formula wherein R<SP>1</SP> is defined as for R and m is 0-3, the ratio of mercapto groups in (1) to the vinyl groups in (2) being 1 : 100 to 100 : 1, and (3) a photosensitizer, the composition being applied to a substrate and cured with ultra-violet light of wavelength 2537 Š. Preferred compositions are those in which y is 1, R and R<SP>1</SP> contain 1-6 carbon atoms (especially methyl), R<SP>2</SP> is a propylene radical, R<SP>4</SP> and R<SP>5</SP> are methyl radicals, z and m are 2, n is 1, and x is 0 or 1.
SE7401593A 1973-09-28 1974-02-06 WAY TREATED PAPER WITH ULTRAVIOLET LIGHT CURED SILOXAN COMPOSITION TO REDUCE ADHESION SE408619B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US40179273A 1973-09-28 1973-09-28

Publications (2)

Publication Number Publication Date
SE7401593L true SE7401593L (en) 1975-04-01
SE408619B SE408619B (en) 1979-06-25

Family

ID=23589244

Family Applications (1)

Application Number Title Priority Date Filing Date
SE7401593A SE408619B (en) 1973-09-28 1974-02-06 WAY TREATED PAPER WITH ULTRAVIOLET LIGHT CURED SILOXAN COMPOSITION TO REDUCE ADHESION

Country Status (9)

Country Link
JP (2) JPS5348198B2 (en)
AT (1) AT338614B (en)
BE (1) BE812515A (en)
CA (1) CA1019693A (en)
DE (2) DE2409384C3 (en)
FR (1) FR2257736B1 (en)
GB (1) GB1433461A (en)
IT (1) IT1008349B (en)
SE (1) SE408619B (en)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4107390A (en) 1977-12-02 1978-08-15 Dow Corning Corporation Radiation-curable organopolysiloxane coating composition comprising mercaptoalkyl and silacyclopentenyl radicals, method of coating and article therefrom
US4201808A (en) 1978-06-12 1980-05-06 Union Carbide Corporation Radiation curable silicone release compositions
US4293678A (en) 1979-11-26 1981-10-06 Union Carbide Corporation Radiation-curable acrylated epoxy silicone compositions
US4369300A (en) 1979-11-26 1983-01-18 Union Carbide Corporation Acrylated urethane silicone compositions
US4447499A (en) * 1983-05-09 1984-05-08 Dow Corning Corporation Method of coating substrates with polydiorganosiloxanes having lower alkyl substituents to provide release coatings
US5169879A (en) * 1983-10-26 1992-12-08 Dow Corning Corporation Fast ultraviolet radiation curing silicone composition
US4923754A (en) * 1983-10-26 1990-05-08 Dow Corning Corporation Fast ultraviolet radiation curing silicone composition
US4780486A (en) * 1983-10-26 1988-10-25 Dow Corning Corporation Fast ultraviolet radiation curing silicone composition
US5124212A (en) * 1983-10-26 1992-06-23 Dow Corning Corporation Articles prepared from fast ultraviolet radiation curing silicone composition
CA1236248A (en) * 1983-10-26 1988-05-03 Dow Corning Corporation Fast ultraviolet radiation curing silicone composition
US5162389A (en) * 1983-10-26 1992-11-10 Dow Corning Corporation Fast ultraviolet radiation curing silicone composition having a high refractive index
JPS60177029A (en) * 1984-02-21 1985-09-11 Toray Silicone Co Ltd Method for curing organopolysiloxane composition
JPS60153979U (en) * 1984-03-27 1985-10-14 工藤 利彦 Pasting bag for cake writing
EP0184598A1 (en) * 1984-12-06 1986-06-18 Toray Silicone Company Limited Ultraviolet and electron-beam curable polyorganosiloxane composition
JPS61143446A (en) * 1984-12-17 1986-07-01 Dainippon Printing Co Ltd Coating material
JPS61162561A (en) * 1985-01-11 1986-07-23 Toray Silicone Co Ltd Organopolysiloxane composition for forming peelable film
US4595635A (en) * 1985-05-02 1986-06-17 Raychem Corporation Organopolysiloxane materials having decreased surface tack
DE3528271A1 (en) * 1985-08-07 1987-02-12 Ego Dichtstoffwerke Sealing strip and process for its manufacture
JP2657249B2 (en) * 1986-11-25 1997-09-24 東レ・ダウコーニング・シリコーン株式会社 Adhesion improver
GB2198740B (en) * 1986-12-22 1991-08-21 Gen Electric Uv-activation of addition cure silicone coatings
US4831064A (en) * 1986-12-22 1989-05-16 Dow Corning Corporation Organopolysiloxane compositions curable by ultraviolet radiation
JPH0642684U (en) * 1992-03-05 1994-06-07 オリエンタル酵母工業株式会社 Squeeze bag
JPH0616944A (en) * 1992-06-29 1994-01-25 Toray Dow Corning Silicone Co Ltd Organopolysiloxane composition for forming peelable cured coating film

Also Published As

Publication number Publication date
DE2409384C3 (en) 1979-05-31
JPS5415487A (en) 1979-02-05
FR2257736B1 (en) 1976-10-08
AT338614B (en) 1977-09-12
CA1019693A (en) 1977-10-25
JPS5348198B2 (en) 1978-12-27
FR2257736A1 (en) 1975-08-08
JPS5061386A (en) 1975-05-26
AU6527774A (en) 1975-08-07
GB1433461A (en) 1976-04-28
DE2409384B2 (en) 1978-10-05
DE2409384A1 (en) 1975-04-10
DE2462750B1 (en) 1980-01-10
DE2462750C2 (en) 1980-09-04
IT1008349B (en) 1976-11-10
JPS5734318B2 (en) 1982-07-22
BE812515A (en) 1974-09-19
ATA167074A (en) 1976-12-15
SE408619B (en) 1979-06-25

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