GB769344A - Improvements in and relating to pigments comprising sulphonamide-melamine-formaldehyde resins - Google Patents

Improvements in and relating to pigments comprising sulphonamide-melamine-formaldehyde resins

Info

Publication number
GB769344A
GB769344A GB32656/54A GB3265654A GB769344A GB 769344 A GB769344 A GB 769344A GB 32656/54 A GB32656/54 A GB 32656/54A GB 3265654 A GB3265654 A GB 3265654A GB 769344 A GB769344 A GB 769344A
Authority
GB
United Kingdom
Prior art keywords
melamine
resin
sulphonamide
toluene
dye
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
GB32656/54A
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.)
Switzer Brothers Inc
Original Assignee
Switzer Brothers Inc
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 Switzer Brothers Inc filed Critical Switzer Brothers Inc
Priority to GB32656/54A priority Critical patent/GB769344A/en
Priority to GB29875/56A priority patent/GB792616A/en
Publication of GB769344A publication Critical patent/GB769344A/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
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/006—Preparation of organic pigments
    • C09B67/0061—Preparation of organic pigments by grinding a dyed resin
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/04—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
    • C08G12/043—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with at least two compounds covered by more than one of the groups C08G12/06 - C08G12/24
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/26—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
    • C08G12/34—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds and acyclic or carbocyclic compounds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Phenolic Resins Or Amino Resins (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

A thermoplastic resin made by co-condensing an aromatic sulphonamide or a C-alkyl derivative thereof having at least two reactive hydrogen atoms attached to N and a formaldehyde condensate of melamine or an alkyl derivative thereof, or an alkanol modified methylol melamine, the melamine condensate containing at least two methylol groups and the amount of same not exceeding 50 per cent by weight of the sulphonamide resin when using a melamine derivative or an alkanol modified melamine, and not exceeding 20 per cent by weight when melamine is used. Specified sulphonamides are o-and p-toluene sulphonamides, benzene sulphonamide or the C-alkyl derivatives thereof. Examples 1 to 6 inclusive describe the preparation of the resin by (1) addition of a partially condensed melamine formaldehyde resin to mixed o- and p-toluene sulphonamides; (2) addition of melamine and formaldehyde to mixed o- and p-toluene sulphonamides; (3) heating together o- and p-toluene sulphonamide, paraformaldehyde and partially condensed melamineformaldehyde resin; (4) adding partially condesned melamineformaldehyde resin to a heated mixture of o- and p-toluene sulphonamide and paraformaldehyde; (5) adding melamine to a heated mixture of o- and p-toluene sulphonamide and formaldehyde; (6) mixing formalin and o- and p-toluene sulphonamide and heating to form a resin to which is added partially condensed melamine-aldehyde resin. The resin, having been ground at temperatures below 100 DEG C., is suitable for use as a pigment with dye or other colouring matter which may be fluorescent, incorporated therein. The dye may be incorporated with the resin: (1) during the cocondensation; (2) by dissolving the resinous product in a solvent, dissolving the dye in the resin solution and then evaporating the solvent; (3) by dissolving the dye in the molten condensation product; (4) by immersing the resinous product in an aqueous dye bath. The resulting pigments may be used as coating compositions or printing inks.
GB32656/54A 1954-11-11 1954-11-11 Improvements in and relating to pigments comprising sulphonamide-melamine-formaldehyde resins Expired GB769344A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB32656/54A GB769344A (en) 1954-11-11 1954-11-11 Improvements in and relating to pigments comprising sulphonamide-melamine-formaldehyde resins
GB29875/56A GB792616A (en) 1954-11-11 1956-10-01 Improvements in and relating to pigments

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB32656/54A GB769344A (en) 1954-11-11 1954-11-11 Improvements in and relating to pigments comprising sulphonamide-melamine-formaldehyde resins
GB29875/56A GB792616A (en) 1954-11-11 1956-10-01 Improvements in and relating to pigments

Publications (1)

Publication Number Publication Date
GB769344A true GB769344A (en) 1957-03-06

Family

ID=62529124

Family Applications (2)

Application Number Title Priority Date Filing Date
GB32656/54A Expired GB769344A (en) 1954-11-11 1954-11-11 Improvements in and relating to pigments comprising sulphonamide-melamine-formaldehyde resins
GB29875/56A Expired GB792616A (en) 1954-11-11 1956-10-01 Improvements in and relating to pigments

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB29875/56A Expired GB792616A (en) 1954-11-11 1956-10-01 Improvements in and relating to pigments

Country Status (1)

Country Link
GB (2) GB769344A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1197183B (en) * 1961-02-02 1965-07-22 Georg Jayme Dr Ing Process for the production of water-resistant organophosphors
US3278486A (en) * 1959-02-17 1966-10-11 Scripto Inc Colored polymeric materials
JPS516698B1 (en) * 1971-03-03 1976-03-01
WO2001098446A1 (en) * 2000-06-19 2001-12-27 Ciba Specialty Chemicals Holding Inc. Fluorescent brightener pigment compositions
WO2007052092A1 (en) * 2005-11-03 2007-05-10 Venuslight Limited Glow in dark composition formula with different after glow colors and methods of processing

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3278486A (en) * 1959-02-17 1966-10-11 Scripto Inc Colored polymeric materials
DE1197183B (en) * 1961-02-02 1965-07-22 Georg Jayme Dr Ing Process for the production of water-resistant organophosphors
JPS516698B1 (en) * 1971-03-03 1976-03-01
WO2001098446A1 (en) * 2000-06-19 2001-12-27 Ciba Specialty Chemicals Holding Inc. Fluorescent brightener pigment compositions
US6936078B2 (en) 2000-06-19 2005-08-30 Ciba Specialty Chemicals Corp. Fluorescent brightener pigment compositions
WO2007052092A1 (en) * 2005-11-03 2007-05-10 Venuslight Limited Glow in dark composition formula with different after glow colors and methods of processing

Also Published As

Publication number Publication date
GB792616A (en) 1958-04-02

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