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GB1471183A - Resin composition - Google Patents

Resin composition

Info

Publication number
GB1471183A
GB1471183A GB2353374A GB2353374A GB1471183A GB 1471183 A GB1471183 A GB 1471183A GB 2353374 A GB2353374 A GB 2353374A GB 2353374 A GB2353374 A GB 2353374A GB 1471183 A GB1471183 A GB 1471183A
Authority
GB
United Kingdom
Prior art keywords
methylol
groups
resin
methylol groups
aminoplast
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
GB2353374A
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.)
Monsanto Co
Original Assignee
Monsanto 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 Monsanto Co filed Critical Monsanto Co
Publication of GB1471183A publication Critical patent/GB1471183A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING 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
    • C09D133/00—Coating 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
    • C09D133/04—Homopolymers or copolymers of esters
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING 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
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04—Homopolymers or copolymers of esters
    • C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • C08L33/08—Homopolymers or copolymers of acrylic acid esters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Paints Or Removers (AREA)
  • Laminated Bodies (AREA)

Abstract

1471183 Powder coating compositions of aminoplasts and hydroxy- or amido-resins MONSANTO CO 28 May 1974 23533/74 Headings C3R and C3P A curable pulverulent resin composition having a sintering temperature of at least 40‹ C. comprises the product of mixing 15-30 p.b.w. of (i) an aminoplast as cross-linking agent with correspondingly 85-70 p.b.w. of (ii) a polymer having alcoholic OH and/or amide groups, wherein the aminoplast (i) has a glass transition temperature of -10‹ to 100‹ C. and is obtained by condensing a methylol- -urea or -aminotriazine having not more than 1 free -NH group per molecule with (a) a C 1-4 aliphatic alcohol and (b) a further alcoholic and/or amido compound of number average molecular less than 500, the molar ratio of methylol compound to reactive groups in (b) being 2 : 1-1 : 2 when (b) is monofunctional, or 2 : 1-1 : 1À5 when (b) is polyfunctional, at least 50% of the methylol groups being condensed with (a) or (b), at least two of them with (a). Preferably the polymer (ii) is of molecular weight 500-10,000 and has a glass transition temperature of 60-100‹ C., and is a polyester of acid number 1-25 and hydroxy number at least 5 or an acrylic copolymer. In Examples 1-9 an MF resin having 5À5 methylol groups (3 methylated) or 5À8 methylol groups (5À5 methylated) per molecule, or a benzoguanamine-formaldehyde resin having 4 methylol groups (2À7 butylated) is condensed i.p.o. citric acid with an equimolar amount of hydrogenated bisphenol A, ethylene glycol, toluenesulphonamide, terephthalamide or benzamide, or with a styrene/allyl alcohol copolymer. In Examples 10, 11, 14 and 15 these are mixed, just above the higher of the two melting points in 3 : 7 or 2 : 8 wt. ratio with a hydroxypolyester from neopentyl glycol, trimethylolethane and isophthalic acid or an acrylic resin from styrene, methyl methacrylate, butyl methacrylate and hydroxyethyl methacrylate or acrylamide, a commercial flow additive and optionally TiO 2 . The cooled products are milled to 20-150 Á and electrostatically sprayed on to steel panels and baked at 175‹ C. for 30 mins.
GB2353374A 1972-12-26 1974-05-28 Resin composition Expired GB1471183A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US31790072A 1972-12-26 1972-12-26

Publications (1)

Publication Number Publication Date
GB1471183A true GB1471183A (en) 1977-04-21

Family

ID=23235740

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2353374A Expired GB1471183A (en) 1972-12-26 1974-05-28 Resin composition

Country Status (4)

Country Link
DE (1) DE2428026A1 (en)
FR (1) FR2273023B3 (en)
GB (1) GB1471183A (en)
NL (1) NL7406796A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002024809A1 (en) * 2000-09-21 2002-03-28 Ppg Industries Ohio, Inc. Aminoplast-based crosslinkers and powder coating compositions containing such crosslinkers
WO2002024799A2 (en) * 2000-09-21 2002-03-28 Ppg Industries Ohio, Inc. Aminoplast-based crosslinkers and powder coating compositions containing such crosslinkers
US6624249B2 (en) 2000-09-21 2003-09-23 Ppg Industries Ohio, Inc. Modified aminoplast crosslinkers and powder coating compositions containing such crosslinkers

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5486530A (en) * 1977-12-21 1979-07-10 Kansai Paint Co Ltd Coating powder composition
AU651007B2 (en) * 1991-10-29 1994-07-07 Courtaulds (Australia) Pty Ltd Solventless coating

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002024809A1 (en) * 2000-09-21 2002-03-28 Ppg Industries Ohio, Inc. Aminoplast-based crosslinkers and powder coating compositions containing such crosslinkers
WO2002024799A2 (en) * 2000-09-21 2002-03-28 Ppg Industries Ohio, Inc. Aminoplast-based crosslinkers and powder coating compositions containing such crosslinkers
WO2002024799A3 (en) * 2000-09-21 2002-08-01 Ppg Ind Ohio Inc Aminoplast-based crosslinkers and powder coating compositions containing such crosslinkers
US6500545B1 (en) 2000-09-21 2002-12-31 Ppg Industries Ohio, Inc. Aminoplast-based crosslinkers and powder coating compositions containing such crosslinkers
US6624249B2 (en) 2000-09-21 2003-09-23 Ppg Industries Ohio, Inc. Modified aminoplast crosslinkers and powder coating compositions containing such crosslinkers
AU2001290999B2 (en) * 2000-09-21 2004-11-18 Ppg Industries Ohio, Inc. Aminoplast-based crosslinkers and powder coating compositions containing such crosslinkers
CN1318486C (en) * 2000-09-21 2007-05-30 Ppg工业俄亥俄公司 Aminoplast-based crosslinkers and powder coating compositions containing such crosslinkers

Also Published As

Publication number Publication date
NL7406796A (en) 1975-11-25
FR2273023B3 (en) 1977-04-08
DE2428026A1 (en) 1976-01-02
FR2273023A1 (en) 1975-12-26

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee