GB756966A - Improvements in or relating to composition of matter - Google Patents

Improvements in or relating to composition of matter

Info

Publication number
GB756966A
GB756966A GB33476/53A GB3347653A GB756966A GB 756966 A GB756966 A GB 756966A GB 33476/53 A GB33476/53 A GB 33476/53A GB 3347653 A GB3347653 A GB 3347653A GB 756966 A GB756966 A GB 756966A
Authority
GB
United Kingdom
Prior art keywords
silica
isocyanate
finely divided
toluene
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
GB33476/53A
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.)
Columbia Southern Chemical Corp
Original Assignee
Columbia Southern Chemical 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 Columbia Southern Chemical Corp filed Critical Columbia Southern Chemical Corp
Publication of GB756966A publication Critical patent/GB756966A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • C08K9/04Ingredients treated with organic substances
    • 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
    • C09C1/00Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/28Compounds of silicon
    • C09C1/30Silicic acid
    • C09C1/3063Treatment with low-molecular organic compounds
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00Crystal-structural characteristics
    • C01P2002/04Compounds with a limited amount of crystallinty, e.g. as indicated by a crystallinity index
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/50Agglomerated particles
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/60Particles characterised by their size
    • C01P2004/62Submicrometer sized, i.e. from 0.1-1 micrometer
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/60Particles characterised by their size
    • C01P2004/64Nanometer sized, i.e. from 1-100 nanometer
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/12Surface area
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/80Compositional purity
    • C01P2006/82Compositional purity water content
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/90Other properties not specified above

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Nanotechnology (AREA)
  • Composite Materials (AREA)
  • Polymers & Plastics (AREA)
  • Physics & Mathematics (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Materials Engineering (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

Synthetic rubber compositions comprise the product obtained by heating together an organic isocyanate and finely divided silica having an average particle size below 0.1 micron and containing bound water corresponding to the formula H2O(SiO2)x where x is 3 to 85. The synthetic rubber may be a polymer of butadiene - 1,3, isoprene, piperylene, 2,3-dimethyl butadiene, 2-chlorobutadiene-1,3, or a copolymer of these monomers with acrylonitrile, vinyl chloride, vinyl acetate, styrene, methyl methacrylate, methyl alpha-chloracrylate, methyl acrylate or isobutylene. The silica may be made from calcium silicate by treatment with hydrochloric acid (see Group III). Examples describe the use of toluene 2,4-diisocyanate, octodecyl isocyanate, phenyl isocyanate, toluene diisocyanate partially reacted with trimethylol propane, tri-p-phenylisocyanate methane, and methylene bis-(4-phenylisocyanate). The compositions may be vulcanized. Specification 756,857, [Group III], is referred to.ALSO:A finely divided material which may be used as a filler for natural and synthetic rubber (see Groups IV(a) and V) comprises the product obtained by heating together an organic isocyanate, and finely divided silica having an average particle size below 0.1 micron and containing bound water corresponding to the formula H2O(SiO2)x where x is 3 to 85. The silica preferably consists of at least 85 per cent. SiO2, and has a surface area of 25-200 square metres per gram. The silica is preferably made by reacting calcium silicate with hydrochloric acid although hypochlorous acid, hydrobromic acid, nitric acid, nitrous acid and acetic acid may also be used. The resulting product may be calcined at about 600 DEG C. In examples the finely divided silica is treated with toluene 2, 4 - diisocyanate, octadecyl isocyanate, phenyl isocyanate, toluene diisocyanate partially reacted with trimethylol propane, tri-pphenylisocyanate methane, or methylene bis (4-phenylisocyanate) dissolved in carbon tetrochloride and then dried at 105 DEG C. About 0.25 to 20 per cent. by weight of isocyanate based on the silica is normally used. Specification 756,857 is referred to.ALSO:Natural rubber compositions comprise the product obtained by heating together an organic isocyranate, and finely divided silica having an average particle size below 0.1 micron and containing bound water corresponding to the formula H2O (Si O2)x where x is 3 to 85. The silica which preferably contains bound water may be made from calcium silicate by treatment with hydrochloric acid as described in Group III. Many isocyanates are specified and the following are used in examples, toluene 2, 4-diisocyanate, octodecyl isocyanate, phenyl isocyanate, toluene diiscocyanate partially reacted with trimethylol propane, tri-p-phenylisocyanate methane, and methylene bis (4-phenylisocyanate). In Examples XV and XVI one of the above isocyanates was dissolved in carbon tetrachloride and then the solution slurried with finely divided silica, and then the solvent removed at 105 DEG C. The treated silica was then added to a mixture consisting of natural rubber, zinc oxide, sulphur, stearic acid, agerite powder, diorthotol guanidine and benzothiazyl dissulphide. Specification 756,857 [Group III] is referred to.
GB33476/53A 1952-12-10 1953-12-02 Improvements in or relating to composition of matter Expired GB756966A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US756966XA 1952-12-10 1952-12-10

Publications (1)

Publication Number Publication Date
GB756966A true GB756966A (en) 1956-09-12

Family

ID=22127412

Family Applications (1)

Application Number Title Priority Date Filing Date
GB33476/53A Expired GB756966A (en) 1952-12-10 1953-12-02 Improvements in or relating to composition of matter

Country Status (2)

Country Link
DE (1) DE1076649B (en)
GB (1) GB756966A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1103576A1 (en) * 1999-11-23 2001-05-30 The Goodyear Tire & Rubber Company Rubber compositions containing a silica-formamide complex

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR954737A (en) * 1950-01-05
DE953010C (en) * 1951-10-15 1956-11-22 Degussa Filler for rubber and plastic compounds

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1103576A1 (en) * 1999-11-23 2001-05-30 The Goodyear Tire & Rubber Company Rubber compositions containing a silica-formamide complex
US6274655B1 (en) 1999-11-23 2001-08-14 The Goodyear Tire & Rubber Company Rubber compositions containing a silica-formamide complex

Also Published As

Publication number Publication date
DE1076649B (en) 1960-03-03

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