GB738589A - Improved waxes and compositions containing them - Google Patents

Improved waxes and compositions containing them

Info

Publication number
GB738589A
GB738589A GB20508/52A GB2050852A GB738589A GB 738589 A GB738589 A GB 738589A GB 20508/52 A GB20508/52 A GB 20508/52A GB 2050852 A GB2050852 A GB 2050852A GB 738589 A GB738589 A GB 738589A
Authority
GB
United Kingdom
Prior art keywords
silicon
alcohol
organo
wax
acid
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
GB20508/52A
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.)
Wacker Chemie AG
Original Assignee
Wacker Chemie AG
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
Priority claimed from DEW6533A external-priority patent/DE897158C/en
Application filed by Wacker Chemie AG filed Critical Wacker Chemie AG
Publication of GB738589A publication Critical patent/GB738589A/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
    • C09GPOLISHING COMPOSITIONS; SKI WAXES
    • C09G1/00Polishing compositions
    • C09G1/06Other polishing compositions
    • C09G1/08Other polishing compositions based on wax
    • C09G1/10Other polishing compositions based on wax based on mixtures of wax and natural or synthetic resin
    • C09G1/12Other polishing compositions based on wax based on mixtures of wax and natural or synthetic resin mixtures of wax and silicon-containing polycondensates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • C08L91/06Waxes

Landscapes

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

Abstract

Wax compositions comprise a mixture of a wax and a polymeric hydrocarbon-substituted organo-silicon compound which contains aliphatic radicals having at least 14 carbon atoms, which may contain ether linkages and which are bound to silicon through an -O- or -OCO-bridge. The compounds may be hydrocarbon-substituted organo-silicon compounds, e.g. silicone derivatives, in which have been introduced the residues of higher fatty alcohols or higher fatty acids. The organo-silicon compounds may be prepared by heating a siloxane oil containing alkyl, aryl or aralkyl radicals, silicon-bonded hydrogen or alkoxy or acyloxy groups with a higher alcohol or a higher fatty acid. In examples, an alkyl-siloxane oil containing one SiH group for every two silicon atoms and a methyl-siloxane oil having every eleventh silicon atom bound to a hydrogen atom are heated at 150-250 DEG C. with cetyl alcohol, octadecyl alcohol or a polyethylene oxide containing hydroxyl groups. A catalyst or substance of alkaline or acid reaction may be present, e.g. a sodium alcoholate, zinc chloride or an ansolvo acid. In further examples, an alkyl-silicone oil containing the group -SiOC2H5 and another containing the group -SiOCOCH3 are reacted with cetyl alcohol or octadecyl alcohol. Other organo-silicon compounds may be used, such as silmethylenes or silphenylenes or polysilanes, containing residues of higher alcohols or higher acids.ALSO:Silanes containing the residues of aliphatic alcohols or acids having at least 14 carbon atoms may be prepared by reacting an alkoxysilane or a silane containing a silicon-bonded hydrogen atom with the appropriate alcohol or acid. In an example, cetyl alcohol is refluxed with trimethylbutoxysilane to interchange the butoxy and cetyloxy groups.ALSO:Wax compositions comprise a mixture of a wax and a monomeric or polymeric hydrocarbon-substituted organo-silicon compound which contains aliphatic radicals having at least 14 carbon atoms, which may contain ether linkages and which are bound to silicon through an -O- or -OCO-bridge. The compounds may be hydrocarbon-substituted organo-silicon compounds, e.g. silicone derivatives, in which have been introduced the residues of higher fatty alcohols or higher fatty acids. The waxes specified comprise paraffin wax, ceresin wax, carnauba, candellila, montan and brown wax. The organo-silicon compounds may be prepared by heating a siloxane oil containing alkyl, aryl or aralkyl radicals with a higher alcohol or a higher fatty acid. Hydrogen is evolved and SiH groups are converted into SiOR1 or SiOCOR1 groups, in which R1 represents the residue of the higher alcohol or higher acid. In examples, an alkyl-siloxane oil containing one SiH-group for every two silicon atoms and a methyl-siloxane oil having every eleventh silicon atom bound to a hydrogen atom are reacted with cetyl alcohol, octadecyl alcohol or a polyethylene oxide containing hydroxyl groups. A catalyst or substance of alkaline or acid reaction may be present, e.g. a sodium alcoholate, zinc chloride or an ansolvo acid. Temperatures of 150-250 DEG C. are exemplified. The organo-silicon compounds may also be prepared from silicones containing lower alkoxy groups by reetherification with higher alcohols, or from silicones containing lower acyloxy groups by reaction with higher fatty alcohols, or from alkoxy-silicones by reaction with higher fatty acids. In examples, an alkyl-silicone oil containing the group -SiOC2H5 and another containing the group p -SiOCOCH3 are reacted with cetyl alcohol or octadecyl alcohol. Other organo silicon compounds may be used, such as silmethylenes or silphenylenes or polysilanes, containing residues of higher alcohols or higher acids. The wax compositions may also contain modifying additions such as resins, fatty oils, fatty acids or emulsifying agents. The compositions may be used alone or with other materials as polishes or coating compositions.
GB20508/52A 1951-08-18 1952-08-14 Improved waxes and compositions containing them Expired GB738589A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE1061446X 1951-08-18
DE738589X 1951-08-18
DEW6533A DE897158C (en) 1951-08-18 1951-08-19 Process for improving waxes, paraffins and mixtures of waxy substances

Publications (1)

Publication Number Publication Date
GB738589A true GB738589A (en) 1955-10-19

Family

ID=31191548

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20508/52A Expired GB738589A (en) 1951-08-18 1952-08-14 Improved waxes and compositions containing them

Country Status (2)

Country Link
FR (1) FR1061446A (en)
GB (1) GB738589A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3222200A (en) * 1960-01-08 1965-12-07 Emblem Harold Garton Compositions for imparting water-repellent properties to fibrous materials
US3271305A (en) * 1961-09-01 1966-09-06 Dan River Mills Inc Textile treatments and treated textiles
EP0274100A2 (en) * 1986-12-22 1988-07-13 Wacker Silicones Corporation Sulfur containing organopolysiloxane waxes and a method for preparing the same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3222200A (en) * 1960-01-08 1965-12-07 Emblem Harold Garton Compositions for imparting water-repellent properties to fibrous materials
US3271305A (en) * 1961-09-01 1966-09-06 Dan River Mills Inc Textile treatments and treated textiles
EP0274100A2 (en) * 1986-12-22 1988-07-13 Wacker Silicones Corporation Sulfur containing organopolysiloxane waxes and a method for preparing the same
EP0274100A3 (en) * 1986-12-22 1990-09-12 Wacker Silicones Corporation Sulfur containing organopolysiloxane waxes and a method for preparing the same

Also Published As

Publication number Publication date
FR1061446A (en) 1954-04-12

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