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GB1039871A - Coated inorganic and organic substrate materials - Google Patents

Coated inorganic and organic substrate materials

Info

Publication number
GB1039871A
GB1039871A GB264163A GB264163A GB1039871A GB 1039871 A GB1039871 A GB 1039871A GB 264163 A GB264163 A GB 264163A GB 264163 A GB264163 A GB 264163A GB 1039871 A GB1039871 A GB 1039871A
Authority
GB
United Kingdom
Prior art keywords
siloxane
radical
hydrocarbon radical
oxyalkylene
block
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
GB264163A
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.)
Union Carbide Corp
Original Assignee
Union Carbide Corp
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 Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB1039871A publication Critical patent/GB1039871A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B13/00Oxygen; Ozone; Oxides or hydroxides in general
    • C01B13/14Methods for preparing oxides or hydroxides in general
    • C01B13/145After-treatment of oxides or hydroxides, e.g. pulverising, drying, decreasing the acidity
    • 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
    • C08G77/46Block-or graft-polymers containing polysiloxane sequences containing polyether sequences
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09CTREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C3/00Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
    • C09C3/12Treatment with organosilicon compounds
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/647Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/10Particle morphology extending in one dimension, e.g. needle-like

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Paints Or Removers (AREA)
  • Silicon Polymers (AREA)

Abstract

Inorganic oxide materials, e.g. silica, mica, quartz, sand, tale, diatomaceous earth, clays, asbestos, crystalline zeolites, iron oxides, zinc oxide, aluminium oxide, calcium oxide, chromium oxide, barium oxide and titanium dioxide, and calcium carbonate, are rendered water resistant and antistatic by coating them with a polysiloxane-oxyalkylene block copolymer comprising (a) at least one siloxane block containing at least two siloxane units represented by the formula <FORM:1039871/C1/1> in which R is a monovalent hydrocarbon radical, a halogen-substituted monovalent hydrocarbon radical or a divalent hydrocarbon radical and b is 1, 2 or 3, the siloxane block containing at least one siloxane unit in which at least one R is a divalent hydrocarbon radical and (b) at least one oxyalkylene block containing at least two oxyalkylene groups represented by the formula -R1O- in which R1 is an alkylene radical, the siloxane and oxyalkylene blocks being interconnected by the divalent hydrocarbon radical. Preferably each R radical contains 1-20 carbon atoms, the R radicals being the same or different in any given siloxane group or throughout the siloxane block and the value of b in the various siloxane groups in the siloxane block being the same or different. When R is a monovalent hydrocarbon radical it may be an alkenyl, cyclo alkenyl, alkyl, aryl, aralkyl, alkaryl or cyclo alkyl radical and when R is a divalent hydrocarbon radical it may be an alkylene, arylene or alkarylene radical. The siloxane block may contain organic chain-terminating groups as well as the mono-functional hydrocarbon radicals, e.g. hydroxyl, aryloxy, alkoxy and acyloxy radicals, and one or more siloxane groups having the formula <FORM:1039871/C1/2> in which R is as defined above, e is 0, 1 or 2, f is 1 or 2 and (e + f) is 1, 2 or 3. The radical R1 in the oxyalkylene block may contain 2-10 carbon atoms and the oxyalkylene block may also contain chain-terminating groups, e.g. hydroxy, aryloxy, alkoxy, alkenyl oxy radicals or the glyceroxy group <FORM:1039871/C1/3> The inorganic oxide materials may be in the form of powders or fibres and the copolymer may be applied in the form of an aqueous emulsion or solution in a volatile organic liquid, e.g. ethers, aliphatic, aromatic or halogenated hydrocarbons, or carbon disulphide, and the treated materials then heated at a temperature of 50-200 DEG C. for from 5 minutes to 24 hours. The coating composition may also contain nonionic, anionic or cationic emulsifying agents and curing catalysts, e.g. salts of lead, tin, zinc, copper, zirconium or titanium with lauric, palmitic, oleic stearic, coconut fatty acid or 2-ethylhexoic acid.ALSO:Fabrics, paper, leather and furs are coated with a polysiloxane-oxyalkylene block copolymer comprising (a) at least one siloxane block containing at least two siloxane units represented by the formula <FORM:1039871/B1-B2/1> in which R is a monovalent hydrocarbon radical, a halogen-substituted monovalent hydrocarbon radical or a divalent hydrocarbon radical and b is 1, 2 or 3, the siloxane block containing at least one siloxane unit in which at least one R is a divalent hydrocarbon radical and (b) at least one oxyalkylene block containing at least two oxyalkylene groups represented by the formula -R1O- in which R1 is an alkylene radical, the siloxane and oxyalkylene blocks being interconnected by the divalent hydrocarbon radical. Preferably each R radical contains 1-20 carbon atoms, the R radicals being the same or different in any given siloxane group or throughout the siloxane block and the value of b in the various siloxane groups in the siloxane block being the same or different. When R is a monovalent hydrocarbon radical it may be an alkenyl, cyclo alkenyl, alkyl, aryl aralkyl, alkaryl or cyclo alkyl radical and when R is a divalent hydrocarbon radical it may be an alkylene, arylene or alkarylene radical. The siloxane block may contain organic chain-terminating groups as well as the mono-functional hydrocarbon radicals, e.g. hydroxyl, aryloxy, alkoxy and acyloxy radicals, and one or more siloxane groups having the formula <FORM:1039871/B1-B2/2> in which R is as defined above, e is 0, 1 or 2, f is 1 or 2 and (e + f) is 1, 2 or 3. The radical R1 in the oxyalkylene block may contain 2-10 carbon atoms and the oxyalkylene block may also contain chain-terminating groups, e.g. hydroxy, aryloxy, alkoxy, alkenyl oxy radicals or the glyceroxy group <FORM:1039871/B1-B2/3> Fabrics made from cotton, linen, ramie, hemp, jute, cellulose ether, cellulose acetate, viscose rayon, cuprammonium rayon, glass, asbestos, natural silk, tussore silk, wool, polyamide, acrylic, vinyl, vinylidene, polyester and polyethylene fibres, may be treated. The materials may be coated by immersing, brushing or spraying them with the copolymer in the form of aqueous emulsion of solution in a volatile organic liquid, e.g. ethers, aliphatic, aromatic or halogenated hydrocarbons, or carbon disulphide, and then heating at a temperature of 50-200 DEG C for from 5 minutes to 24 hours. The coating composition may also contain nonionic, anionic or cationic emulsifying agents and curing catalysts, e.g. salts of lead, tin, zinc, copper, zirconium or titanium with lauric, palmitic, oleic, stearic, coconut fatty acid or 2, ethylhexoic acid.ALSO:Textile materials are rendered water repellant, soft, antistatic, soil resistant, crease resistant and dimensionally stable and are lubricated by coating them with a polysiloxane-oxyalkylene block copolymer comprising (a) at least one siloxane block containing at least two siloxane units represented by the formula Rb Si O4-b/2 in which R is a monovalent hydrocarbon radical, a halogen-substituted monovalent hydrocarbon radical or a divalent hydrocarbon radical and b is 1, 2, or 3, the siloxane block containing at least one siloxane unit in which at least one R is a divalent hydrocarbon radical and (b) at least one oxyalkylene block containing at least two oxyalkylene groups represented by the formula -R1O- in which R1 is an alkylene radical, the siloxane and oxyalkylene blocks being interconnected by the divalent hydrocarbon radical. Preferably each R radical contains 1-20 carbon atoms, the R radicals being the same or different in any given siloxane group or throughout the siloxane block and the value of b in the various siloxane groups in the siloxane block being the same or different. When R is a monovalent hydrocarbon radical it may be an alkenyl, cyclo alkenyl, alkyl, aryl, aralkyl, alkaryl or cyclo alkyl radical and when R is a divalent hydrocarbon radical it may be an alkylene, arylene or alkarylene radical. The siloxane block may contain organic chain-terminating groups as well as the mono-functional hydrocarbon radicals, e.g. hydroxyl, aryloxy, alkoxy and acyloxy radicals, and one or more siloxane groups having the formula <FORM:1039871/D1-D2/1> in which R is as defined above, e is 0, 1 or 2, f is 1 or 2 and (e + f) is 1, 2 or 3. The radical R1 in the oxyalkylene block may contain 2-10 carbon atoms and the oxyalkylene block may also contain chain-terminating groups, e.g. hydroxy, aryloxy, alkoxy, alkenyl oxy radicals or the glyceroxy group <FORM:1039871/D1-D2/2> The textile materials, e.g. cotton, linen, ramie, hemp, jute, cellulose ether, cellulose acetate, viscose rayon, cuprammonium rayon, glass, asbestos, natural silk, tussore silk, wool, polyamide, acrylic, vinyl, vinylidene, polyester and polyethylene fibres, may be in the form of filaments, rovings, yarns, mats or cloth. The materials may be coated by immersing, brushing or spraying them with the copolymer in the form of an aqueous emulsion or solution in a volatile organic liquid, e.g. ethers, aliphatic, aromatic or halogenated hydrocarbons, or carbon disulphide, and then heating at a temperature of 50 DEG -200 DEG C. for from 5 minutes to 24 hours. The coating composition may also contain nonionic, anionic or cationic emulsifying agents and curing catalysts, e.g. salts of lead, tin, zinc, copper, zirconium or titanium with lauric, palmitic, oleic, stearic, coconut fatty acid or 2, ethylhexoic acid.
GB264163A 1962-01-24 1963-01-22 Coated inorganic and organic substrate materials Expired GB1039871A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16851462A 1962-01-24 1962-01-24
US16852562A 1962-01-24 1962-01-24

Publications (1)

Publication Number Publication Date
GB1039871A true GB1039871A (en) 1966-08-24

Family

ID=26864200

Family Applications (1)

Application Number Title Priority Date Filing Date
GB264163A Expired GB1039871A (en) 1962-01-24 1963-01-22 Coated inorganic and organic substrate materials

Country Status (2)

Country Link
DE (1) DE1444133A1 (en)
GB (1) GB1039871A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2437383A1 (en) * 1978-09-28 1980-04-25 Dow Corning LIME TREATMENT WITH SILOXANES TO IMPROVE ITS FLOW PROPERTIES
FR2439809A1 (en) * 1978-10-25 1980-05-23 Toray Silicone Co IMPROVING AGENT BASED ON ZINC OXIDE AND A SILICON COMPOUND ON ELECTRICAL INSULATORS, PROCESS FOR PRODUCING THE SAME, AND ELECTRICALLY INSULATING COMPOSITION CONTAINING THE SAME
EP0924239A1 (en) * 1997-12-22 1999-06-23 General Electric Company Durable hydrophilic coating for textiles
GB2355453A (en) * 1999-10-20 2001-04-25 Dow Corning Preparing hydrophobic calcium carbonate by surface treating with a siloxane
CN103087551A (en) * 2013-02-04 2013-05-08 道奇威(成都)科技有限公司 Surface modification method for improving hydrophobicity and temperature resistance of calcium carbonate for plastics

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2437383A1 (en) * 1978-09-28 1980-04-25 Dow Corning LIME TREATMENT WITH SILOXANES TO IMPROVE ITS FLOW PROPERTIES
FR2439809A1 (en) * 1978-10-25 1980-05-23 Toray Silicone Co IMPROVING AGENT BASED ON ZINC OXIDE AND A SILICON COMPOUND ON ELECTRICAL INSULATORS, PROCESS FOR PRODUCING THE SAME, AND ELECTRICALLY INSULATING COMPOSITION CONTAINING THE SAME
EP0924239A1 (en) * 1997-12-22 1999-06-23 General Electric Company Durable hydrophilic coating for textiles
US6630415B2 (en) 1997-12-22 2003-10-07 General Electric Company Durable hydrophilic coating for textiles
GB2355453A (en) * 1999-10-20 2001-04-25 Dow Corning Preparing hydrophobic calcium carbonate by surface treating with a siloxane
CN103087551A (en) * 2013-02-04 2013-05-08 道奇威(成都)科技有限公司 Surface modification method for improving hydrophobicity and temperature resistance of calcium carbonate for plastics

Also Published As

Publication number Publication date
DE1444133A1 (en) 1969-10-02

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