GB1114579A - Inks for ball point pens - Google Patents

Inks for ball point pens

Info

Publication number
GB1114579A
GB1114579A GB3747965A GB3747965A GB1114579A GB 1114579 A GB1114579 A GB 1114579A GB 3747965 A GB3747965 A GB 3747965A GB 3747965 A GB3747965 A GB 3747965A GB 1114579 A GB1114579 A GB 1114579A
Authority
GB
United Kingdom
Prior art keywords
dye
component
formula
copolymer
ink
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
GB3747965A
Inventor
Klaus Gulbins
Guenter Lange
Hans Wilhelm
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik AG
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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB1114579A publication Critical patent/GB1114579A/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
    • C09D11/00Inks
    • C09D11/16Writing inks
    • C09D11/18Writing inks specially adapted for ball-point writing instruments

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

A ball-point pen ink comprises a solution in a high boiling point organic solvent of a coloured copolymer which has been prepared from: (a) an aromatic monoethylenically unsaturated compound and/or (b) an ester of a monoethylenically unsaturated carboxylic acid and (c) a dye bearing an ethylenically unsaturated group, by copolymerization of (a) and/or (b) and (c) component (c) may be replaced by: (c) a monoethylenically unsaturated monomer bearing a reactive group and the copolymer obtained is reacted with: (f) a dye bearing a reactive group complementary to the reactive group borne by component (e). In another modification, component (c) is replaced by: (g) a monoethylinecally unsaturated diazotizable monomer and the copolymer obtained is diazotized and then reacted with (h) a coupling component, to form a polymer dye. The coloured copolymer may contain units of (d) one or more further monomers. The high boiling points solvent has a boiling point of not less than 125 DEG C., those specified being 1,2-propylene carbonate, dicyclohexyl carbonate, diphenyl carbonate, adipate and phthalic esters such as diethyl or di-n-butyl phthalate, methyl glycol, ethyl glycol and benzyl alcohol. Monomer (a) is e.g. styrene or a substituted styrene, for instance p-methyl, p-chloro, o-chloro or p-hydroxystyrene. Specified monomers (b) include ethyl, n-butyl, cyclohexyl, 2-ethylhexyl and stearylacrylates, and methylmethacrylate. Suitable dyes (c) are azo, anthraquinone or triphenylmethane dyes containing a vinyl, acrylyl, acrylylamino, acryloyloxyalkyl or acrylyloxyaryl group. Component (e) may be acrylamide, methacrylamide or a derivative thereof and component (g) may be p-aminostyrene. In the examples, ethyl acrylate or methyl methacrylate are copolymerized with a dye of formula <FORM:1114579/C3/1> in solution in n-butyl acetate using azodiisobutyrodinitril as catalyst. Benzyl alcohol is added to the resulting solution, from which the butyl acetate is then removed by distillation, to yield a red ink. When methyl methacrylate is similarly copolymerized with a dye of formula <FORM:1114579/C3/2> an orange-red ink is obtained, with a dye of formula <FORM:1114579/C3/3> a yellow ink is obtained and with a dye of formula <FORM:1114579/C3/4> a violet ink is obtained.
GB3747965A 1964-09-03 1965-09-02 Inks for ball point pens Expired GB1114579A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB78365A DE1264651B (en) 1964-09-03 1964-09-03 Ballpoint pen pastes

Publications (1)

Publication Number Publication Date
GB1114579A true GB1114579A (en) 1968-05-22

Family

ID=6979847

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3747965A Expired GB1114579A (en) 1964-09-03 1965-09-02 Inks for ball point pens

Country Status (3)

Country Link
BE (1) BE669112A (en)
DE (1) DE1264651B (en)
GB (1) GB1114579A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0396376B1 (en) * 1989-05-02 1994-12-28 BAUSCH &amp; LOMB INCORPORATED Polymerizable dye

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4471079A (en) * 1982-03-04 1984-09-11 Pilot Man-Nen Hitsu Kabushiki Kaisha Aqueous ink
DE4422335A1 (en) 1994-06-27 1996-01-04 Basf Ag Dye preparations

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0396376B1 (en) * 1989-05-02 1994-12-28 BAUSCH &amp; LOMB INCORPORATED Polymerizable dye

Also Published As

Publication number Publication date
DE1264651B (en) 1968-03-28
BE669112A (en) 1966-03-02

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