GB869801A - Improvements in and relating to pigments comprising sulphonamide-aminotriazine-formaldehyde resins - Google Patents

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

Info

Publication number
GB869801A
GB869801A GB29589/58A GB2958958A GB869801A GB 869801 A GB869801 A GB 869801A GB 29589/58 A GB29589/58 A GB 29589/58A GB 2958958 A GB2958958 A GB 2958958A GB 869801 A GB869801 A GB 869801A
Authority
GB
United Kingdom
Prior art keywords
diamino
resin
triazine
pigment
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
GB29589/58A
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
Publication of GB869801A publication Critical patent/GB869801A/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
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B69/00Dyes not provided for by a single group of this subclass
    • C09B69/10Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/26Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
    • C08G12/34Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds and acyclic or carbocyclic compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

A pigment comprises a dye incorporated with a finely divided thermoplastic resinous co-condensation product of (a) at least one aryl monosulphonamide having two reactive hydrogen atoms attached to N with (b) a diamino-1, 3, 5-triazine or a C-alkyl, aryl or aralkyl derivative thereof, and formaldehyde or with an alkanolmodified methylol derivative of the triazine, the alkanol containing up to eight carbon atoms. The dye may be incorporated into the resin before or after grinding. The sulphonamide and the aminotriazine may be separately combined with formaldehyde before co-condensation. Suitable sulphonamides are o- and p-toluene sulphonamides. Diamino-1, 3, 5-triazines mentioned are 2, 4-diamino-; 2-methyl-4, 6-diamino-; 2(3-hydroxybutyl)-4, 6-diamino-; 2-heptyl-4, 6-diamino-; 2-phenyl-4, 6-diamino-; and 2-benzyl-4, 6-diamino-triazine. If desired the aminotriazine may be introduced as a solution in an alkanol, and modified with the alkanol during the course of condensation. Preferred dyestuffs are fluorescent, e.g. the rhodamines and naphthalimides. In examples mixed o- and p-toluene sulphonamides are treated with paraformaldehyde and the mixture reacted with additional formaldehyde and with (1) 2-phenyl-4, 6-diamino-1, 3, 5-triazine; (2) 2-benzyl-4, 6-diamino-1, 3, 5-triazine, and (3) 2-(b -cyanoethyl)-4, 6-diamino-1, 3, 5-triazine. Examples 4-9 illustrate the introduction of various fluorescent dyestuffs into the molten resins of Examples 1-3. Titanium dioxide, lithopone or chrome yellow or a colourless ultra-violet light absorber such as benzophenone may also be added to the compositions. In Example 10 powdered resin is dyed in a dye-bath. In Example 11 acetone solutions of dye and resin are mixed, the solvent removed and the dyed resin ground. The remaining examples illustrate compositions containing the coloured resins, as follows:-(12) as pigment in an ink vehicle containing alkyd resin, aluminium stearate gel, driers and mineral spirits; (13) as pigment in an ink based on a petroleum solution of styrene-butadiene resin containing methyl dihydroabietate or of polystyrene-cyclised rubber mixture; (15) as a pigment in an alkyd paint; (16) as pigment in a flexible paint based on a xylol solution of chloro-sulphonated polyethylene; (17) as pigment in a plastisol of vinyl chloridevinyl acetate co-polymer with dioctyl phthalate and dioctyl sebacate as plasticizers, and an epoxy resin stabilizer; thinning this composition with naphtha yields an organosol. In Example 18 the coloured resin is dissolved with cellulose butyrate and dioctyl phthalate in methyl ethyl ketone, ethyl acetate and toluene to give a wood-coating composition.
GB29589/58A 1958-06-11 1958-09-16 Improvements in and relating to pigments comprising sulphonamide-aminotriazine-formaldehyde resins Expired GB869801A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US869801XA 1958-06-11 1958-06-11

Publications (1)

Publication Number Publication Date
GB869801A true GB869801A (en) 1961-06-07

Family

ID=22202105

Family Applications (1)

Application Number Title Priority Date Filing Date
GB29589/58A Expired GB869801A (en) 1958-06-11 1958-09-16 Improvements in and relating to pigments comprising sulphonamide-aminotriazine-formaldehyde resins

Country Status (1)

Country Link
GB (1) GB869801A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS516698B1 (en) * 1971-03-03 1976-03-01
US5989453A (en) * 1990-05-11 1999-11-23 Societe Nouvelle De Chimie Industrielle S.A. Process for the manufacture of pigments, especially fluorescent pigments
WO2001098446A1 (en) * 2000-06-19 2001-12-27 Ciba Specialty Chemicals Holding Inc. Fluorescent brightener pigment compositions

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS516698B1 (en) * 1971-03-03 1976-03-01
US5989453A (en) * 1990-05-11 1999-11-23 Societe Nouvelle De Chimie Industrielle S.A. Process for the manufacture of pigments, especially fluorescent pigments
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

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