GB862602A - Organopolysiloxane compositions suitable for use as protective varnishes - Google Patents

Organopolysiloxane compositions suitable for use as protective varnishes

Info

Publication number
GB862602A
GB862602A GB26434/59A GB2643459A GB862602A GB 862602 A GB862602 A GB 862602A GB 26434/59 A GB26434/59 A GB 26434/59A GB 2643459 A GB2643459 A GB 2643459A GB 862602 A GB862602 A GB 862602A
Authority
GB
United Kingdom
Prior art keywords
methyl
ratio
bonded
siloxane
content
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
GB26434/59A
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.)
Rhone Poulenc SA
Original Assignee
Rhone Poulenc SA
Societe des Usines Chimiques Rhone Poulenc SA
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 Rhone Poulenc SA, Societe des Usines Chimiques Rhone Poulenc SA filed Critical Rhone Poulenc SA
Publication of GB862602A publication Critical patent/GB862602A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D183/00Coating compositions based on 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; Coating compositions based on derivatives of such polymers
    • C09D183/04Polysiloxanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04Polysiloxanes
    • C08G77/14Polysiloxanes containing silicon bound to oxygen-containing groups
    • C08G77/16Polysiloxanes containing silicon bound to oxygen-containing groups to hydroxyl groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04Polysiloxanes
    • C08G77/14Polysiloxanes containing silicon bound to oxygen-containing groups
    • C08G77/18Polysiloxanes containing silicon bound to oxygen-containing groups to alkoxy or aryloxy groups
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Silicon Polymers (AREA)
  • Paints Or Removers (AREA)

Abstract

A varnish for protecting painted surfaces comprises by weight (a) 30 to 60% of at least one siloxane having an average R/Si ratio of 1.2 to 1.6 and containing an average of 0.5 to 2.5% of Si-bonded hydroxyl groups, (b) 1 to 25% of a monomeric or polymeric methyl or ethyl silicate, (c) 1 to 20% of at least one organic solvent-soluble titanic or zirconic ester or condensation polymer thereof, (d) 0 to 20% of an organic solvent-soluble organic zinc salt, and (e) at least 15% of a solvent for all the above. The siloxane may contain methyl, ethyl, butyl or phenyl radicals and may also contain -Si.Si- and -Si.CH2.Sigroups. Suitable esters (c) are those derived from alcohols containing from 2 to 18 C atoms, e.g. isopropyl, butyl and octyl titanates. In typical examples: (1) methyl polysilicate and zinc 2-ethylhexoate in white spirit were added to a mixture of a mineral spirit solution of a methyl siloxane resin having a ratio CH3/Si=1.5 and a Si-bonded OH content of 0.3% (by wt.) and a toluene solution of another methyl siloxane resin having a ratio CH3/Si=1.3 and a Si-bonded OH content of 3.2%, and the resulting solution was heated to 80 DEG C. with the subsequent addition of a butyl acetate solution of a butyl polytitanate and further heating until a clear liquid was obtained; (3) the composition was prepared as in (1) except that the siloxane resins were replaced by a methyl phenyl siloxane resin having a ratio C6H5 + CH3/Si=1.5, C6H5/Si=0.3 and a Si-bonded OH content of 0.5% and a methyl siloxane resin having a ratio CH3/Si=1.5, a Si-bonded OH content of 1% and -Si.Sigroups, as described in Specification 736,971.
GB26434/59A 1958-08-05 1959-07-31 Organopolysiloxane compositions suitable for use as protective varnishes Expired GB862602A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR862602X 1958-08-05

Publications (1)

Publication Number Publication Date
GB862602A true GB862602A (en) 1961-03-15

Family

ID=9342898

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26434/59A Expired GB862602A (en) 1958-08-05 1959-07-31 Organopolysiloxane compositions suitable for use as protective varnishes

Country Status (1)

Country Link
GB (1) GB862602A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1244400B (en) * 1962-05-17 1967-07-13 Dow Corning One-component molding compounds that can be stored in the absence of moisture and hardened to elastomers in the air at room temperature
FR2474518A1 (en) * 1980-01-14 1981-07-31 Toray Silicone Co Room temp. curing silicone resin compsn. - giving flexible anti-adhesion coatings, can be stored under anhydrous conditions

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1244400B (en) * 1962-05-17 1967-07-13 Dow Corning One-component molding compounds that can be stored in the absence of moisture and hardened to elastomers in the air at room temperature
FR2474518A1 (en) * 1980-01-14 1981-07-31 Toray Silicone Co Room temp. curing silicone resin compsn. - giving flexible anti-adhesion coatings, can be stored under anhydrous conditions

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