GB893821A - Improvements in or relating to flushed pigments in powder form - Google Patents

Improvements in or relating to flushed pigments in powder form

Info

Publication number
GB893821A
GB893821A GB1946/59A GB194659A GB893821A GB 893821 A GB893821 A GB 893821A GB 1946/59 A GB1946/59 A GB 1946/59A GB 194659 A GB194659 A GB 194659A GB 893821 A GB893821 A GB 893821A
Authority
GB
United Kingdom
Prior art keywords
mixture
pigment
sulfonic acid
flushing agent
water
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
GB1946/59A
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.)
Sandoz AG
Original Assignee
Sandoz 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 Sandoz AG filed Critical Sandoz AG
Publication of GB893821A publication Critical patent/GB893821A/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
    • C09CTREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C3/00Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
    • C09C3/003Flushing

Abstract

A process for the production of pigment compositions comprises mixing an aqueous pigment dispersion with a flushing agent which is solid at normal air temperatures, this flushing agent being an ester of a di- or tri-basic carboxylic acid or an alkylbenzene sulfonic acid amide or a mixture of such esters and/or amides, heating the resulting mixture to a temperature at which said flushing agent liquefies and the water is set free from the dispersion, separating the freed water from the mixture and if desired cooling the resulting flushed pigment mixture to solidify the same and pulverizing the mixture. Suitable flushing agents specified are dicyclohexyl phthalate, a mixture of 2- and 4-methylbenzene-1-sulfonic acid amides, 4-methylbenzene-1-sulfonic acid cyclohexylamide, tricyclohexyl citrate, di-isobutyl tartrate and the glycerin ester of colophony. If desired any water remaining after the separation step can be eliminated by drying in a drying cabinet or by kneading in a vacuum kneading machine. In examples the process is applied to a copper phthalocyanine blue pigment, a copper phthanocyanine green pigment, a chlorinated phthalocyanine green pigment and a red pigment Naphthol AS. Examples are also given of compositions prepared according to the invention containing ethyl cellulose, a vinyl polymer and an acrylic resin. The products may be used in lacquers, printing inks and cellulose acetate fibres.ALSO:A process for the production of pigment compositions comprises mixing an aqueous pigment dispersion with a flushing agent which is solid at normal air temperatures this flushing agent being an ester of a di- or tri-basic carboxylic acid or an alkylbenzene sulfonic acid amide or a mixture of such esters and/or amides, heating the resulting mixture to a temperature at which said flushing agent liquefies and the water is set free from the dispersion, separating the freed water from the mixture and if desired cooling the resulting flushed pigment mixture to solidify the same and pulverizing the mixture. Suitable flushing agents specified are dicyclohexyl phthalate a mixture of 2- and 4-methylbenzene-1-sulfonic acid amides, 4-methylbenzene-1-sulfonic acid cyclohexylamide, tricyclohexyl citrate, di-isobutyl tartrate and the glycerin ester of colophony. If desired any water remaining after the separation step can be eliminated by drying in a drying cabinet or by kneading in a vacuum kneading machine. In examples the process is applied to a copper phthalocyanine blue pigment, a copper phthalocyanine green pigment a chlorinated phthalocyanine green pigment and a red pigment Naphthol AS. Examples are also given of compositions prepared according to the invention containing ethyl cellulose, a vinyl polymer ("Vinylite" VMCH) (Registered Trade Mark) and an acrylic resin. The products may be used in lacquers, printing inks and cellulose acetate fibres.ALSO:A process for the production of pigment compositions comprises mixing an aqueous pigment dispersion with a flushing agent which is solid at normal air temperatures this flushing agent being as ester of a di- or tri-basic carboxylic acid or an alkylbenzene sulfonic acid amide or a mixture of such esters and/or amides, heating the resulting mixture to a temperature at which said flushing agent liquefies and the water is set free from the dispersion, separating the freed water from the mixture and if desired cooling the resulting flushed pigment mixture to solidify the same and pulverising the mixture. Suitable flushing agents specified are dicyclohexyl phthalate a mixture of 2- and 4-methylbenzene-1-sulfonic acid amides, 4-methylbenzene-1-sulfonic acidcyclohexylamide, tricyclohexyl citrate, di-isobutyl tartrate and the glycerin ester of colophony. If desired any water remaining after the separation step can be eliminated by drying in a drying cabinet or by kneading in a vacuum kneading machine. In examples the process is applied to a copper phthalocyanine blue pigment, a copper phthalocyanine green pigment a chlorinated phthalocyanine green pigment and a red pigment Naphthol AS. p Examples are also given of compositions prepared according to the invention containing ethyl cellulose, a vinyl polymer and an acrylic resin. The products may be used in lacquers, printing inks and cellulose acetate fibres.
GB1946/59A 1958-01-20 1959-01-19 Improvements in or relating to flushed pigments in powder form Expired GB893821A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CH1222659X 1958-01-20
CH5483758A CH369243A (en) 1958-01-20 1958-01-20 Process for the production of pigment preparations
CH893821X 1958-01-20

Publications (1)

Publication Number Publication Date
GB893821A true GB893821A (en) 1962-04-11

Family

ID=61198453

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1946/59A Expired GB893821A (en) 1958-01-20 1959-01-19 Improvements in or relating to flushed pigments in powder form

Country Status (3)

Country Link
CH (1) CH369243A (en)
FR (1) FR1222659A (en)
GB (1) GB893821A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4729796A (en) * 1980-10-21 1988-03-08 Hoechst Aktiengesellschaft Process for preparing pigment granules from aqueous suspension of pigment and alkaline solution of resin
US6423376B1 (en) 2000-04-06 2002-07-23 Air Products And Chemicals, Inc. Tartaric acid diesters as biodegradable surfactants
WO2012140647A3 (en) * 2011-04-11 2013-03-28 Yeda Research And Development Co. Ltd Albumin binding probes and drug conjugates thereof

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4729796A (en) * 1980-10-21 1988-03-08 Hoechst Aktiengesellschaft Process for preparing pigment granules from aqueous suspension of pigment and alkaline solution of resin
US6423376B1 (en) 2000-04-06 2002-07-23 Air Products And Chemicals, Inc. Tartaric acid diesters as biodegradable surfactants
US6544591B2 (en) 2000-04-06 2003-04-08 Air Products And Chemicals, Inc. Tartaric acid diesters as biodegradable surfactants
US6585814B2 (en) 2000-04-06 2003-07-01 Air Products And Chemicals, Inc. Tartaric acid diesters as biodegradable surfactants
WO2012140647A3 (en) * 2011-04-11 2013-03-28 Yeda Research And Development Co. Ltd Albumin binding probes and drug conjugates thereof
US9480751B2 (en) 2011-04-11 2016-11-01 Yeda Research And Development Co. Ltd. Albumin binding probes and drug conjugates thereof

Also Published As

Publication number Publication date
CH369243A (en) 1963-05-15
FR1222659A (en) 1960-06-13

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