GB529399A - Improvements in or relating to coating film forming and sealing compositions obtained from polymeric derivatives of methacrylic acid - Google Patents

Improvements in or relating to coating film forming and sealing compositions obtained from polymeric derivatives of methacrylic acid

Info

Publication number
GB529399A
GB529399A GB14767/39A GB1476739A GB529399A GB 529399 A GB529399 A GB 529399A GB 14767/39 A GB14767/39 A GB 14767/39A GB 1476739 A GB1476739 A GB 1476739A GB 529399 A GB529399 A GB 529399A
Authority
GB
United Kingdom
Prior art keywords
wax
polymer
esters
methacrylic acid
solution
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
GB14767/39A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB529399A publication Critical patent/GB529399A/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
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/10Homopolymers or copolymers of methacrylic acid esters
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/24Homopolymers or copolymers of amides or imides
    • C09D133/26Homopolymers or copolymers of acrylamide or methacrylamide
    • 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)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

529,399. Synthetic resin compositions. DU PONT DE NEMOURS & CO., E. I. May 17, 1939, No. 14767. Convention date, May 20, 1938. [Class 2 (iii)] Coating, film forming, sealing compositions &c. are obtained by blending together a wax and a polymeric methacrylic acid amide, imide or ester, the wax and the polymer being heated together above the melting point of the wax, and the polymer when it is an ester, being such that the alkyl radical thereof contains more than two carbonatoms. Waxes include those of animal; vegetable, or mineral origin such as carnauba candellila, montan, lanoline, cocabutter, cotton seed, stearin, Japan wax, bayberry, myrtle, mace, palm kernel, beeswax, spermaceti, Chinese insect, mutton tallow, hydrogenated coconut oils, soy bean, paraffin, ceresin, montan, ozokerite. Of the esters of methacrylic acid n-propyl and higher esters are suitable e.g. butyl, cyclohexyl, amino alcohol esters, esters of mixtures of alcohols obtained by the catalytic hydrogenation of carbon oxides at elevated pressure, methacrylic acid esters of alcohols derived by carboxyl hydrogenation of vegetable oils eg. lauryl, myristyl, cetyl and stearyl alcohols. Polymeric amides and imides specified comprise the laurylimide, octylimide, monobutyl amide, dibutyl amide and the mono- and di-higher-alkylamides. Interpolymers or polymeric mixtures may also be used provided the average of the number of carbon atoms in the alkyl groups is greater than 2. Additional components specified comprise natural or synthetic rubbers or their halogen compounds, gutta percha, asphalt, natural and synthetic resins and plasticizers e.g. dicyclohexyl phthalate, phthalates of higher alcohols, cresyl phosphates para toluene sulphonamide, dibutyl phthalates, octadecanediol monocarbamate, stearyl carbamate. The temperatures specified are from 75‹C. upwards but preferably temperatures above the " solution temperature " of the ester, i.e. the temperature at which the paraffinpolymer solution becomes cloudy on cooling. This decreases with increasing molecular weight of the esterified alcohol radical e.g. the solution " temperature for a 40 per cent. polymer solution of propyl methacrylate in paraffin wax is 240‹C. and 170‹C. for butyl methacrylate. 40 parts of n-butyl methacrylate monomer (containing 0.5 per cent. benzoyl peroxide) is mixed with 60 parts of melted paraffin wax (m.p. 57-60‹C. ) and the mixture placed in an oven heated to 100‹C. After three days the layers of polymer and paraffin are heated to 180‹C. and complete solution is obtained. A table of blends of paraffin wax, polymer and additional ingredients is given. The products obtained may be used (1) as coating compositions for cloth, paper, leather, cellulose films, linoleum oil cloth, wall board, stone, cement, bricks &c. wood, glass, metals, wire screens (2) in the form of films and filaments which may be used for wrapping foodstuffs &c. Alternatively the food stuffs may be dipped in the molten products (3) for spraying wood, metal, cans for preserving food &c. and for electric insulation purposes (4) as adhesives or polishes (5) for sizing paper.
GB14767/39A 1938-05-20 1939-05-17 Improvements in or relating to coating film forming and sealing compositions obtained from polymeric derivatives of methacrylic acid Expired GB529399A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US529399XA 1938-05-20 1938-05-20

Publications (1)

Publication Number Publication Date
GB529399A true GB529399A (en) 1940-11-20

Family

ID=21980896

Family Applications (1)

Application Number Title Priority Date Filing Date
GB14767/39A Expired GB529399A (en) 1938-05-20 1939-05-17 Improvements in or relating to coating film forming and sealing compositions obtained from polymeric derivatives of methacrylic acid

Country Status (1)

Country Link
GB (1) GB529399A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3171825A (en) * 1959-06-11 1965-03-02 Western Petrochemical Corp Novel polymerized compositions of a wax, hydrocarbon polymer and a polymeric polar organic compound
US3246963A (en) * 1963-02-01 1966-04-19 Exxon Research Engineering Co Compositions containing wax and either a wax-naphthalene condensation product or certain fumarate ester containing polymers
US4990561A (en) * 1989-01-20 1991-02-05 Shin-Etsu Chemical Co., Ltd. Wax composition and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3171825A (en) * 1959-06-11 1965-03-02 Western Petrochemical Corp Novel polymerized compositions of a wax, hydrocarbon polymer and a polymeric polar organic compound
US3246963A (en) * 1963-02-01 1966-04-19 Exxon Research Engineering Co Compositions containing wax and either a wax-naphthalene condensation product or certain fumarate ester containing polymers
US4990561A (en) * 1989-01-20 1991-02-05 Shin-Etsu Chemical Co., Ltd. Wax composition and preparation method thereof

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