GB980583A - Fluorescent, dyed resinous condensation products - Google Patents

Fluorescent, dyed resinous condensation products

Info

Publication number
GB980583A
GB980583A GB551461A GB551461A GB980583A GB 980583 A GB980583 A GB 980583A GB 551461 A GB551461 A GB 551461A GB 551461 A GB551461 A GB 551461A GB 980583 A GB980583 A GB 980583A
Authority
GB
United Kingdom
Prior art keywords
sulphonamide
dyed
fluorescent
resin
specified
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
GB551461A
Inventor
Edward Tozer
Geoffrey Harry Lloyd-Sherlock
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.)
IND COLOURS Ltd
Original Assignee
IND COLOURS 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 IND COLOURS Ltd filed Critical IND COLOURS Ltd
Priority to GB551461A priority Critical patent/GB980583A/en
Publication of GB980583A publication Critical patent/GB980583A/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
    • C09B67/00Influencing 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
    • C09B67/006Preparation of organic pigments
    • C09B67/0061Preparation of organic pigments by grinding a dyed resin
    • 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
    • C08G12/04Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
    • C08G12/043Condensation 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
    • C08G12/046Condensation 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 one being urea or thiourea

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Fluorescent, dyed and thermoplastic amideformaldehyde resins are produced by a process which comprises adding a fluorescent dye to a resin, produced by co-condensing (a) an aryl sulphonamide having at least two reactive hydrogen atoms, (b) urea, thiourea or an aliphatic compound containing two or more groups in which an amino group is attached to carbonyl, and (c) formaldehyde or a substance generating formaldehyde under the conditions of the condensation, by heating the substances together in the presence of an aliphatic or alicyclic organic base, either during or after the co - condensation. Aryl sulphonamides specified are toluene p-sulphonamide, benzene sulphonamide, a -naphthalene sulphonamide, b - naphthalene sulphonamide and alkylnaphthalene sulphonamides. Compounds specified containing two amino groups attached to carbonyl are succinamide and malonamide, and paraformaldehyde is specified as the substance yielding formaldehyde. Bases specified are hexamethylenetetramine and triethanolamine. In examples resins prepared by heating a mixture of toluene p-sulphonamide, urea and paraformaldehyde with either hexamethylenetetramine or triethanolamine are dyed by adding Azosol Brilliant Yellow 6GF with or without the addition of xanthene type dyes to the molten reaction mixture or warming the powdered resin in an aqueous dye bath containing xanthene type dyes, formic acid and the iso-octyl ether of polyethylene glycol. A dyed resin of the invention is used as pigment in a fluorescent ink suitable for silk screen printing comprising also a long oil alkyd resin based on pentaerythritol, white spirit and a mixture of calcium and cobalt naphthenate. A fluorescent lacquer is obtained by dissolving a dyed resin in diacetone alcohol. Reference has been directed by the Comptroller to Specification 792,616.
GB551461A 1961-02-14 1961-02-14 Fluorescent, dyed resinous condensation products Expired GB980583A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB551461A GB980583A (en) 1961-02-14 1961-02-14 Fluorescent, dyed resinous condensation products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB551461A GB980583A (en) 1961-02-14 1961-02-14 Fluorescent, dyed resinous condensation products

Publications (1)

Publication Number Publication Date
GB980583A true GB980583A (en) 1965-01-13

Family

ID=9797648

Family Applications (1)

Application Number Title Priority Date Filing Date
GB551461A Expired GB980583A (en) 1961-02-14 1961-02-14 Fluorescent, dyed resinous condensation products

Country Status (1)

Country Link
GB (1) GB980583A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0456610A1 (en) * 1990-05-11 1991-11-13 Societe Nouvelle De Chimie Industrielle S.A. A process for the manufacture of pigments
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
WO2004083313A1 (en) * 2003-03-20 2004-09-30 Mca Technologies Gmbh Process for the preparation of fluorescent and non-fluorescent pigments

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0456610A1 (en) * 1990-05-11 1991-11-13 Societe Nouvelle De Chimie Industrielle S.A. A process for the manufacture of pigments
FR2661917A1 (en) * 1990-05-11 1991-11-15 Chimie Indle Sa Ste Nle PIGMENTS, METHOD AND DEVICE FOR MANUFACTURING THE SAME.
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
WO2004083313A1 (en) * 2003-03-20 2004-09-30 Mca Technologies Gmbh Process for the preparation of fluorescent and non-fluorescent pigments

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