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GB628150A - New polymerisable materials and polymers thereof - Google Patents

New polymerisable materials and polymers thereof

Info

Publication number
GB628150A
GB628150A GB382647A GB382647A GB628150A GB 628150 A GB628150 A GB 628150A GB 382647 A GB382647 A GB 382647A GB 382647 A GB382647 A GB 382647A GB 628150 A GB628150 A GB 628150A
Authority
GB
United Kingdom
Prior art keywords
products
acrylic
weight
acid
groups
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
GB382647A
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.)
ROY HAMMOND
Imperial Chemical Industries Ltd
Original Assignee
ROY HAMMOND
Imperial Chemical Industries 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 ROY HAMMOND, Imperial Chemical Industries Ltd filed Critical ROY HAMMOND
Priority to GB382647A priority Critical patent/GB628150A/en
Publication of GB628150A publication Critical patent/GB628150A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B26/00Compositions of mortars, concrete or artificial stone, containing only organic binders, e.g. polymer or resin concrete
    • C04B26/02Macromolecular compounds
    • C04B26/04Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C04B26/06Acrylates
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00612Uses not provided for elsewhere in C04B2111/00 as one or more layers of a layered structure

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Polymerizable products are obtained by reacting, under conditions such that polymerization is inhibited, one or more monohydroxy acrylic, including methacrylic and a -haloacrylic, esters with one or more compounds containing 3 or more methylol or alkoxymethyl groups attached ortho and/or para in a hydroxy and/or amino-substituted aromatic ring or to a nitrogen atom attached to a >CO, >CS or >C=N- group or an aromatic nucleus. Polymerization inhibitors which may be present include copper salts, and anhydrous metal halides as described in Specification 456,147. Suitable polymethylol compounds include trimethylol phenol and aniline, hexamethylol melamine, polymethylol polyamides, and their methyl to butyl ethers. The monohydroxy acrylic esters may be prepared from suitable molecular proportions of an acrylic acid or a lower ester, anhydride or acid chloride thereof, and a di- or poly-hydric alcohol or from a salt of the acid and a hydroxychloride, e.g. ethylene chlorhydrin. Alcohols of not more than 4 hydroxy groups, e.g. ethylene glycol, glycerol, pentaerythritol, trimethylene, propylene, and polyethylene glycols are suitable. Polymerization inhibitors, especially polyhydric phenol sulphonic acids as described in Specification 606,685, [Group IV (b)], or mixtures of copper salts or antimony pentachloride together with strong acids as esterification catalysts, may be present. Preferred polymers are obtained from the products if, based on the weight of reactants less their weight of acrylic groups and the weight of by-products, the weight of hydroxyl groups equivalent to acrylic groups is less than 25, preferably less than 17 per cent, and greater than 1.25, preferably greater than 3.5 per cent. The products have the general formula X.(CH2.O.R.(O.A)q)x, where X is an acryl group having hydroxyl and/or amino substituents in ortho and/or para positions or is nitrogen attached to >CO, >CS, >C=N- or an aromatic nucleus, R is an alkyl group, A an acrylic group, q is 1, 2 or 3, and x an integer above 2. Polymerization may be effected in one or more stages, if desired with other compounds having a C=C linkage such as di-(allyl glycollyl) succinate, glycol dimethacrylate, methyl or butyl methacrylate, vinyl chloride or acetate, styrene, maleic anhydride, polyesters of maleic or fumaric acid and dihydric alcohols, dyes, pigments, fillers and the like being present. Low molecular weight compounds may be added to the polymerizable products to give an average molecular weight of 200-500. The products may be used to bond fibrous materials, particularly glass cloth, to give laminated sheets. In an example, hexamethylol melamine is added to b -hydroxyethyl methacrylate and nitric acid, finally heating to 40 DEG C. and neutralizing. The product freed from volatiles is heated to 100 DEG C. with a solution of benzoyl peroxide in butyl methacrylate, giving a hard resin.ALSO:Polymerizable products are obtained by reacting under conditions such that polymerization is inhibited, one or more monohydroxy acrylic, including methacrylic and a -haloacrylic, esters with one or more compounds containing 3 or more methylol or alkoxymethyl groups attached ortho and/or para in a hydroxy and/or amino-substituted aromatic ring or to a nitrogen atom attached to a >CO, >CS or >C=N- group or an aromatic nucleus. Polymerization inhibitors which may be present include copper salts, and anhydrous metal halides as described in Specification 456,147. Suitable polymethylol compounds include trimethylol phenol and aniline, hexamethylol melamine, polymethylol polyamides, and their methyl to butyl ethers. The monohydroxy acrylic esters may be prepared from suitable molecular proportions of an acrylic acid or a lower ester, anhydride or acid chloride thereof, and a di- or poly-hydric alcohol or from a salt of the acid and a hydroxychloride, e.g. ethylene chlorhydrin. Alcohols of not more than 4 hydroxy groups, e.g. ethylene glycol, glycerol, pentaerythritol, trimethylene, propylene, and polyethylene glycols, are suitable. Water or alcohol liberated may be removed from the reaction mixture by azeotroping. Polymerization inhibitors, especially polyhydric phenol sulphonic acids as described in Specification 606,685, or mixtures of copper salts or antimony pentachloride, together with strong acids as esterification catalysts, may be present. Preferred polymers are obtained from the products if, based on the weight of reactants less their weight of acrylic groups and the weight of by-products, the weight of hydroxyl groups equivalent to acrylic groups is less than 25, preferably less than 17 per cent and greater than 1.25, preferably greater than 3.5 per cent. The products have the general formula X.(CH2.O.R.(O.A)q)x, where X is an aryl group having hydroxyl and/or amino substituents in ortho and/or para positions or is nitrogen attached to >CO, >CS, >C=N-or an aromatic nucleus, R is an alkyl group, A an acrylic group, q is 1, 2 or 3, and x an integer above 2. Polymerization may be effected in one or more stages, if desired with other compounds having a C=C linkage such as di-(allyl glycollyl) succinate, glycol dimethacrylate, methyl or butyl methacrylate, vinyl chloride or acetate, styrene, maleic anhydride, polyesters of maleic or fumaric acid and dihydric alcohols, dyes, pigments, fillers, and the like being present. Low molecular weight compounds may be added to the polymerizable products to give an average molecular weight of 200-500. The products may be used to bond fibrous materials, particularly glass cloth, to give laminated sheets. In an example, hexamethylol melamine is added to b -hydroxyethyl methacrylate and nitric acid, finally heating to 40 DEG C. and neutralizing. The product freed from volatiles, is heated to 100 DEG C. with a solution of benzoyl peroxide in butyl methacrylate, giving a hard resin.
GB382647A 1947-02-10 1947-02-10 New polymerisable materials and polymers thereof Expired GB628150A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB382647A GB628150A (en) 1947-02-10 1947-02-10 New polymerisable materials and polymers thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB382647A GB628150A (en) 1947-02-10 1947-02-10 New polymerisable materials and polymers thereof

Publications (1)

Publication Number Publication Date
GB628150A true GB628150A (en) 1949-08-23

Family

ID=9765659

Family Applications (1)

Application Number Title Priority Date Filing Date
GB382647A Expired GB628150A (en) 1947-02-10 1947-02-10 New polymerisable materials and polymers thereof

Country Status (1)

Country Link
GB (1) GB628150A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2681897A (en) * 1950-10-06 1954-06-22 American Cyanamid Co Surface coating compositions comprising aminoplast resins and a thermoplastic copolymer containing a polymerized hydroxy alkyl ester of an alpha, beta ethylenically unsaturated carboxylic acid
US2819237A (en) * 1953-09-22 1958-01-07 American Cyanamid Co Aqueous dispersions of a copolymer of an ethylenically unsaturated monomer containing a primary hydroxy group and a thermosetting resin forming reaction product
US3304280A (en) * 1962-06-01 1967-02-14 Formica Corp Methyl ethyl ketone solution of a terpolymer of methylmethacrylate, butylacrylate and 2-hydroxyethylmethacrylate
US3539661A (en) * 1966-07-26 1970-11-10 Vianova Kunstharz Ag Process for producing self-curing polymers
US4266053A (en) * 1978-06-21 1981-05-05 Teijin Limited Melamine group-containing (meth)acrylate
US5290893A (en) * 1991-05-20 1994-03-01 Aica Kogyo Co., Ltd. Metharcylate prepolymer containing triazine ring structure, its preparation, and setting composition and resin
DE102008038943A1 (en) 2008-08-11 2010-02-18 Borealis Agrolinz Melamine Gmbh New crosslinkable acrylate resins, useful e.g. to produce crosslinked semi-finished or molded materials for highly stressed parts in automotive, mechanical-, electrical-engineering and electronics, and as crosslinkers in coating resins

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2681897A (en) * 1950-10-06 1954-06-22 American Cyanamid Co Surface coating compositions comprising aminoplast resins and a thermoplastic copolymer containing a polymerized hydroxy alkyl ester of an alpha, beta ethylenically unsaturated carboxylic acid
US2819237A (en) * 1953-09-22 1958-01-07 American Cyanamid Co Aqueous dispersions of a copolymer of an ethylenically unsaturated monomer containing a primary hydroxy group and a thermosetting resin forming reaction product
US3304280A (en) * 1962-06-01 1967-02-14 Formica Corp Methyl ethyl ketone solution of a terpolymer of methylmethacrylate, butylacrylate and 2-hydroxyethylmethacrylate
US3539661A (en) * 1966-07-26 1970-11-10 Vianova Kunstharz Ag Process for producing self-curing polymers
US4266053A (en) * 1978-06-21 1981-05-05 Teijin Limited Melamine group-containing (meth)acrylate
US5290893A (en) * 1991-05-20 1994-03-01 Aica Kogyo Co., Ltd. Metharcylate prepolymer containing triazine ring structure, its preparation, and setting composition and resin
US5296571A (en) * 1991-05-20 1994-03-22 Aica Kogyo Co., Ltd. Methacrylate prepolymer containing triazine ring structure, its preparation, and setting composition and resin
DE102008038943A1 (en) 2008-08-11 2010-02-18 Borealis Agrolinz Melamine Gmbh New crosslinkable acrylate resins, useful e.g. to produce crosslinked semi-finished or molded materials for highly stressed parts in automotive, mechanical-, electrical-engineering and electronics, and as crosslinkers in coating resins

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