GB650247A - Improvements in and relating to alkyd-polysiloxane resins - Google Patents

Improvements in and relating to alkyd-polysiloxane resins

Info

Publication number
GB650247A
GB650247A GB29237/48A GB2923748A GB650247A GB 650247 A GB650247 A GB 650247A GB 29237/48 A GB29237/48 A GB 29237/48A GB 2923748 A GB2923748 A GB 2923748A GB 650247 A GB650247 A GB 650247A
Authority
GB
United Kingdom
Prior art keywords
acids
oil
alkyd resin
heated
methyl
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
GB29237/48A
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.)
British Thomson Houston Co Ltd
Original Assignee
British Thomson Houston Co 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 British Thomson Houston Co Ltd filed Critical British Thomson Houston Co Ltd
Publication of GB650247A publication Critical patent/GB650247A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08G77/42Block-or graft-polymers containing polysiloxane sequences
    • C08G77/445Block-or graft-polymers containing polysiloxane sequences containing polyester sequences
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/08Polyesters modified with higher fatty oils or their acids, or with resins or resin acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Silicon Polymers (AREA)

Abstract

An alkyd-polysiloxane resin is made by mixing an oil-modified alkyd resin containing free OH groups with an organo-polysiloxane containing silicon-bonded alkoxy radicals and heating the mixture with simultaneous removal of the alkanol formed during the reaction. The organo-polysiloxanes used, which may contain from 0.1 to 2.5 methyl and phenyl radicals per silicon atom, are those described in Specifications 542,655, 544,143, 548,911, 548,912 and 551,649 and those of lower molecular weight such as dibutoxy-tetramethyldisiloxane, dipropoxytetramethylcyclo-trisiloxane and dibutoxytetraphenyldisiloxane, and may be made by heating organoalkoxysilanes, e.g. methyltripropoxy-, methyltributoxy-, dimethyldibutoxy-, tri - isopropylpropoxy-, diethyldihexoxy-, phenyltributoxy-, diphenyldibutoxy- and methylphenyldipentoxysilanes, with an acid catalyst (e.g. in amount of 0.1 to 6.0 per cent by weight) such as glacial acetic acid and sufficient water to remove the alkoxy radicals, or by hydrolysing and alcoholizing an organohalogenosilane with sufficient alcohol and water to remove the halogen but insufficient to complete the hydrolysis. The alkyd resin may be made from one or more polybasic acids, e.g. oxalic, malonic, succinic, glutaric, adipic, tricarballylic, phthalic, isophthalic, terephthalic and 4-chloro-phthalic acids or their anhydrides, and a molar excess of a polyhydric alcohol, e.g. ethylene-, diethylene-, propylene- and trimethylene glycols, glycerine, trimethylolpropane, pentaerythritol, polyallyl alcohol, sorbitol and mannitol, and modified by oils (5 to 80 per cent by weight), in the raw, heated or blown state, e.g. linseed, rapeseed, cottonseed, chinawood, castor (excluding the raw oil), dehydrated castor, soyabean, perilla, oiticica, linseed oil acids, coconut oil fatty acids, ricinoleic acid, glycerides of linoleic and linolenic acids, palmitic, oleic and stearic acids, babassu oil, palm oil, fish oils and fish oil acids such as clupanodonic, and fatty oil acids derived therefrom. In examples, a butoxy phenyl polysiloxane in xylene is heated with an alkyd resin made from (1) glycerine, phthalic anhydride, coconut oil acids and xylene; (2) pentaerythritol, phthalic anhydride, coconut oil acids and xylol, enamels (3) being made therefrom by the addition of xylene and titania; (4) the alkyd resin of (1) was heated with a polysiloxane of the formula <FORM:0650247/IV (a)/1> , where X is an integer >1, prepared from methyltrichloro- and dimethyldichloro-silanes and butanol; the alkyd resin of example (2) is heated with (5) <FORM:0650247/IV (a)/2> and with (6) <FORM:0650247/IV (a)/3> ; (8) the alkyd resin of (2), but containing more pentaerythritol, is heated with <FORM:0650247/IV (a)/4> prepared from dimethyldichlorosilane, butanol and the catalyst FeCl3.6H2O. Other resins, e.g. rosin, shellac, kauri, dammar, coumaroneindene, phenolic or other alkyd resins and mixtures thereof may be added to the compositions. Other solvents, or mixtures thereof, specified are: methyl cyclo-hexanone, methyl isobutyl ketone, mesityl oxide, methyl-n-amyl ketone, di-isobutyl ketone, glycol diacetate, butyl lactate, tetralin, benzene, butanol, benzyl alcohol, nitromethane, 1-nitropropane, 2-nitropropane, the nitrobutanes, the nitropentanes, carbon tetrachloride, pentachlorethane, ethylene dichloride, and the ethyl and butyl ethers of ethylene glycol. Specification 583,754 also is referred to. The Specification as open to inspection under Sect. 91 comprises also using a liquid methyl polysiloxane containing silicon-bonded alkoxy groups as a modifying ingredient in place of oily modifying ingredients employed in alkyd resin manufacture, this, in example (9), phthalic anhydride, pentaerythritol, liquid methyl butoxysiloxane (as in example (8)) and xylene are heated together. This subject-matter does not appear in the Specification as accepted.ALSO:Organoalkoxysilanes, e.g. methyltripropoxysilane, methyltributoxysilane, dimethyldibutoxysilane, tri-isopropylpropoxysilane, diethyldihexoxysilane, phenyltributoxysilane, diphenyldibutoxysilane and methylphenyldipentoxysilane, are made by adding the particular organohalogenosilane to at least an equivalent amount of a primary alcohol.
GB29237/48A 1947-11-22 1948-11-10 Improvements in and relating to alkyd-polysiloxane resins Expired GB650247A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US650247XA 1947-11-22 1947-11-22

Publications (1)

Publication Number Publication Date
GB650247A true GB650247A (en) 1951-02-21

Family

ID=22059836

Family Applications (1)

Application Number Title Priority Date Filing Date
GB29237/48A Expired GB650247A (en) 1947-11-22 1948-11-10 Improvements in and relating to alkyd-polysiloxane resins

Country Status (1)

Country Link
GB (1) GB650247A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE896980C (en) * 1950-08-30 1953-11-16 Siemens Ag Process for the production of burn-in silicone paints
US2686739A (en) * 1951-05-31 1954-08-17 Dow Corning Insulated electrical conductor and method of producing same
US2686740A (en) * 1951-05-31 1954-08-17 Dow Corning Insulated electrical conductor and method of producing same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE896980C (en) * 1950-08-30 1953-11-16 Siemens Ag Process for the production of burn-in silicone paints
US2686739A (en) * 1951-05-31 1954-08-17 Dow Corning Insulated electrical conductor and method of producing same
US2686740A (en) * 1951-05-31 1954-08-17 Dow Corning Insulated electrical conductor and method of producing same

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