GB958081A - Pressure operative transfer sheets containing treated pigments - Google Patents

Pressure operative transfer sheets containing treated pigments

Info

Publication number
GB958081A
GB958081A GB476262A GB476262A GB958081A GB 958081 A GB958081 A GB 958081A GB 476262 A GB476262 A GB 476262A GB 476262 A GB476262 A GB 476262A GB 958081 A GB958081 A GB 958081A
Authority
GB
United Kingdom
Prior art keywords
solution
pigment
mixed
cetylamine
dispersion
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
GB476262A
Inventor
Raymond Deverell-Smith
Hugh Patrick Dryhurst Paget
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB476262A priority Critical patent/GB958081A/en
Priority to DEJ23131A priority patent/DE1225480B/en
Priority to CH147063A priority patent/CH434529A/en
Priority to FR924073A priority patent/FR1348085A/en
Priority to AT96263A priority patent/AT252965B/en
Publication of GB958081A publication Critical patent/GB958081A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/10Duplicating or marking methods; Sheet materials for use therein by using carbon paper or the like
    • 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
    • C09B67/0001Post-treatment of organic pigments or dyes
    • C09B67/002Influencing the physical properties by treatment with an amine
    • 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
    • C09C3/08Treatment with low-molecular-weight non-polymer organic compounds
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/60Particles characterised by their size
    • C01P2004/61Micrometer sized, i.e. from 1-100 micrometer

Abstract

A process for making carbon black pigment more oleophilic comprises mixing a watersoluble salt of an amine containing at least one chain of at least 10 carbon atoms with a dispersion of the pigment in an aqueous solution of a carboxylic acid salt which has a deflocculating action on the pigment dispersion. The amine salt may be the hydrochloride or acetate of decylamine, dodecylamine, cetylamine, oleylamine, N-oleylpropylenediamine or a mixture obtained by reduction of the nitriles from carboxylic acid mixtures from natural sources. The carboxylic acid salt may be the alkali metal, ammonium, ethanolamine or triethanolamine salts of stearic, palmitic, oleic, linoleic, myristic or abietic acids, polymers of linoleic acid, rosin, modified rosins or tall oil. 90% of the pigment particles may be less than 2 microns in diameter. The oil may be mineral, animal or vegetable oils. In Examples 1, 3 and 4 an aqueous dispersion of carbon black is mixed with potassium rosinate solution and a solution in acetic acid of a mixture of amines obtained by reduction of the mixed nitriles from tallow fatty acids, and cetylamine or N-olelylpropylene diamine with or without mineral oil. The pigments in dry or paste form, are mixed with mineral oil, toluene, methyl ethyl ketone and a copolymer of vinyl chloride and vinyl acetate, and the resultant composition applied to paper tissues.ALSO:A composition for coating paper tissues to produce waxless carbon papers comprises a mixture of a pigment-oil dispersion with a solution of a copolymer of vinyl chloride and vinyl acetate, which pigment has been made more oleophilic by mixing a water-soluble salt of an amine containing at least one chain of at least 10 carbon atoms with a dispersion of the pigment in an aqueous solution of a carboxylic acid salt which has a deflocculating action on the pigment dispersion. The amine salt may be the hydrochloride or acetate of decylamine, dodecylamine, cetylamine, oleylamine, N-oleylpropylenediamine or a mixture obtained by reduction of the nitriles from carboxylic acid mixtures from natural sources. The carboxylic acid salt may be the alkali metal, ammonium, ethanolamine or triethanolamine salts of stearic, palmitic oleic, linoleic, myrietic or abietic acids, polymers of linoleic acid, rosin, modified rosine or tall oil. The pigment may be carbon black or an organic pigment of the azophthalocyanine, anthraquinone, thioindigoid or polycyclic series. 90% of the pigment particles may be less than 2 microns in diameter. The oil may be mineral, animal or vegetable oils. In Examples 1, 3 and 4 an aqueous dispersion of carbon black is mixed with potassium rosinate solution and a solution in acetic acid of a mixture of amines obtained by reduction of the mixed nitriles from tallow fatty acids, and cetylamine or N-oleylpropylene diamine with or without mineral oil. In Examples 5 and 6 an aqueous paste of copper chlorophthalocyanine is mixed with a solution in potassium hydroxide of dibasic fatty acids obtained by dimerisation of naturally occurring fatty acids containing 18 carbon atoms per molecule and a solution of cetylamine in dilute acetic acid with or without mineral oil. In Example 7 an aqueous paste of Rubine Toner is mixed with sodium dodecyl benzenesulphonate solution, potassium rosinate solution and a solution of cetylamine in acetic acid. The pigments in dry or paste form, are mixed with mineral oil, toluene, methyl ethyl ketone and a copolymer of vinyl chloride and vinyl acetate, and the resultant composition applied to paper tissues.ALSO:A process for making pigments more oleophilic comprises mixing a water-soluble salt of an amine containing at least one chain of at least 10 carbon atoms with a dispersion of a pigment in an aqueous solution of a carboxylic acid salt which has a deflocculating action on the pigment dispersion. The amine salt may be the hydrochloride or acetate of decylamine, dodecylamine, cetylamine, oleylamine, N-oleylpropylenediamine or a mixture obtained by reduction of the nitriles from carboxylic acid mixtures from natural sources. The carboxylic acid salt may be the alkali metal, ammonium, ethanolamine or triethanolamine salts of stearic, palmitic oleic, linoleic, myristic or abietic acids, polymers of linoleic acid, rosin, modified rosins or tall oil. The pigment may be carbon black or an organic pigment of the azo, phthalocyanine, anthraquinone, thioindigoid or polycyclic series, 90% of the pigment particles may be less than 2 microns in diameter. The oil may be mineral, animal or vegetable oils. In Examples 1, 3 and 4, an aqueous dispersion of carbon black is mixed with potassium rosinate solution and a solution in acetic acid of a mixture of amines obtained by reduction of the mixed nitriles from tallow fatty acids, and cetylamine or N-olelylpropylene diamine with or without mineral oil. In Examples 5 and 6 an aqueous paste of copper chlorophthalocyanine is mixed with a solution in potassium hydroxide of dibasic fatty acids obtained by dimerization of naturally occurring fatty acids containing 18 carbon atoms per molecule and a solution of cetylamine in dilute acetic acid with or without mineral oil. In Example 7 an aqucous paste of Rubine Toner is mixed with sodium dodecyl benzenesulphonate solution, potassium rosinate solution and a solution of cetylamine in acetic acid. The pigments in dry or paste form, are mixed with mineral oil, toluene, methyl ethyl ketone and a copolymer of vinyl chloride and vinyl acetate, and the resultant composition applied to paper tissues.ALSO:Waxless carbon papers are prepared by coating paper tissues with a mixture of a pigment-oil dispersion with a solution of a synthetic polymer, which pigment has been made more oleophilic by mixing a water-soluble salt of an amine containing at least one chain of at least 10 carbon atoms with a dispersion of the pigment in an aqueous solution of a carboxylic acid salt which has a deflocculating action on the pigment dispersion. The amine salt may be the hydrochloride or acetate of decylamine, dodecylamine, cetylamine, oleylamine, N-oleyl-propylenediamine or a mixture obtained by reduction of the nitriles from carboxylic acid mixtures from natural sources. The carboxylic acid salt may be the alkali metal, ammonium, ethanolamine or triethanolamine salts of stearic, palmitic oleic, linoleic, myristic or abietic acids, polymers or linoleic acid, rosin, modified rosins or tall oil. The pigment may be carbon black or an organic pigment of the azo, phthalocyanine, anthraquinone, thioindigoid or polycyclic series. 90% of the pigment particles may be less than 2 microns in diameter. The oil may be mineral, animal or vegetable oils. In Examples 1, 3 and 4 an aqueous dispersion of carbon black is mixed with potassium rosinate solution and a solution in acetic acid of a mixture of amines obtained by reduction of the mixed nitriles from tallow fatty acids, and cetylamine or N-olelylpropylene diamine with or without mineral oil. In Examples 5 and 6 an aqueous paste of copper chlorophthalocyanine is mixed with a solution in potassium hydroxide of dibasic fatty acids obtained by dimerisation of naturally occurring fatty acids containing 18 carbon atoms per molecule and a solution of cetylamine in dilute acetic acid with or without mineral oil. In Example 7 an aqueous paste of Rubine Toner is mixed with sodium dodecyl benzenesulphonate solution, potassium rosinate solution and a solution of cetylamine in acetic acid. The pigments in dry or paste form, are mixed with mineral oil, toluene, methyl ethyl ketone and a copolymer of vinyl chloride and vinyl acetate, and the resultant composition applied to paper tissues.
GB476262A 1962-02-07 1962-02-07 Pressure operative transfer sheets containing treated pigments Expired GB958081A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
GB476262A GB958081A (en) 1962-02-07 1962-02-07 Pressure operative transfer sheets containing treated pigments
DEJ23131A DE1225480B (en) 1962-02-07 1963-02-06 Wax-free carbon paper
CH147063A CH434529A (en) 1962-02-07 1963-02-06 Process for making pigments more oleophilic, pigments and use thereof
FR924073A FR1348085A (en) 1962-02-07 1963-02-07 Process to make pigments more oleophilic
AT96263A AT252965B (en) 1962-02-07 1963-02-07 Process for producing a waxless carbon paper

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB476262A GB958081A (en) 1962-02-07 1962-02-07 Pressure operative transfer sheets containing treated pigments

Publications (1)

Publication Number Publication Date
GB958081A true GB958081A (en) 1964-05-13

Family

ID=9783303

Family Applications (1)

Application Number Title Priority Date Filing Date
GB476262A Expired GB958081A (en) 1962-02-07 1962-02-07 Pressure operative transfer sheets containing treated pigments

Country Status (4)

Country Link
AT (1) AT252965B (en)
CH (1) CH434529A (en)
DE (1) DE1225480B (en)
GB (1) GB958081A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2508383A1 (en) * 1981-06-27 1982-12-31 Pelikan Ag Over-strike ink-ribbon for typewriters - comprises plastic tape coated with polymer contg. dispersion of pigments, etc. in partly aromatic mineral oil
US4515489A (en) * 1981-06-27 1985-05-07 Pelikan Aktiengesellschaft Overstrike ribbon for print wheels
US4544292A (en) * 1982-04-07 1985-10-01 Pelikan Ag Multistrike ribbon
WO1996018456A2 (en) * 1994-12-15 1996-06-20 Cabot Corporation Gel composition containing carbonaceous compound
EP1676889A1 (en) * 2004-12-03 2006-07-05 Toyo Ink Mfg. Co., Ltd. Colored composition

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4599114A (en) * 1985-02-11 1986-07-08 Atkinson George K Treatment of titanium dioxide and other pigments to improve dispersibility

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH199972A (en) * 1937-08-24 1938-09-15 Ringier & Co Aktiengesellschaf Process for the production of non-bleeding and non-smearing carbonless ink films on carriers such as carbonless papers, carbonless forms and the like.
US2852406A (en) * 1954-11-16 1958-09-16 Armour & Co Pigment composition and process for its production

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2508383A1 (en) * 1981-06-27 1982-12-31 Pelikan Ag Over-strike ink-ribbon for typewriters - comprises plastic tape coated with polymer contg. dispersion of pigments, etc. in partly aromatic mineral oil
US4515489A (en) * 1981-06-27 1985-05-07 Pelikan Aktiengesellschaft Overstrike ribbon for print wheels
US4544292A (en) * 1982-04-07 1985-10-01 Pelikan Ag Multistrike ribbon
WO1996018456A2 (en) * 1994-12-15 1996-06-20 Cabot Corporation Gel composition containing carbonaceous compound
WO1996018456A3 (en) * 1994-12-15 1996-08-29 Cabot Corp Gel composition containing carbonaceous compound
US5807494A (en) 1994-12-15 1998-09-15 Boes; Ralph Ulrich Gel compositions comprising silica and functionalized carbon products
US6107350A (en) 1994-12-15 2000-08-22 Cabot Corporation Gel compositions
EP1676889A1 (en) * 2004-12-03 2006-07-05 Toyo Ink Mfg. Co., Ltd. Colored composition
US7156912B2 (en) 2004-12-03 2007-01-02 Toyo Ink Mfg. Co., Ltd. Colored composition
CN100398613C (en) * 2004-12-03 2008-07-02 东洋油墨制造株式会社 Colored composition

Also Published As

Publication number Publication date
DE1225480B (en) 1966-09-22
AT252965B (en) 1967-03-10
CH434529A (en) 1967-04-30

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