Toyo Ink Manufacturing Company

Toyo Ink Mfg. Co., Ltd.

Hitoshi Maki

Shigeki Kato

Kenji Kitamura

Mikio Hayashi

Yoshimi Kikuchi

Hideto Noguchi

Osamu Shiromaru

Ataru Chiba

Masashi Koide

Masami Shirao

Katsuhiko Sawamura

Masayasu Kawamura

Masatoshi Momose

Shoko Goto

Shinichi Azuma

Yoshio Muramatsu

Motoi Shitaka

A process for the production of a colored resin composition, comprising a step (A) of producing an aqueous slurry of a pigment, a step (B) of producing a melting composition of metallocene type polyolefin containing a dispersant and a solvent, a step (C) of kneading the aqueous slurry obtained in the step (A) with the melting composition obtained in the step (B) and a step (D) of removing the solvent and the water from the kneaded mixture obtained in the step (C), a colored composition obtained in the above process has excellent in pigment dispersibility and high color developing properties, a colored resin molded article obtained from the colored resin composition do not give a physical-properties inhibition of 5% or higher and has a color developing properties.

Process for producing colored resin composition and utilization thereof

A monoazo lake pigment composition containing a monoazo lake pigment obtained from a laked pigment aqueous slurry prepared by conducting coupling of a diazo component obtained by diazotizing an aromatic amine having a soluble group and a coupler component and conducting laking after or simultaneously with the coupling, wherein the laking is carried out in the presence of a water-soluble acrylic polymer in an amount of 0.1 to 40 parts by weight per 100 parts of the above coupler component, and a gravure ink containing the above pigment composition and a gravure ink vehicle.

Monoazo lake pigment composition and gravure ink using the same

Disclosed is a method of producing a disazo pigment, which a coupling reaction is carried out while feeding, into an acidic aqueous solution, a tetrazo aqueous solution containing a tetrazo component of benzidines and a coupler aqueous solution containing a coupling component, wherein the coupling component is a mixture comprising a main component represented by the formula (1): CH,COCH,CONH&mdash;X, wherein X represents a phenyl group optionally having one or the same or different plural substituents selected from the group consisting of a methyl group, methoxy group and chlorine atom; a first additional component represented by the formula (2): CH,COCH,CONH&mdash;Y, wherein Y represents a phenyl group having a substituent selected from the group consisting of &mdash;CONR,group, &mdash;SO,NR,group and &mdash;NHCOR group, and the phenyl group may further have a substituent selected from the group consisting of a methyl group, methoxy group, chlorine atom, &mdash;CONR,group, &mdash;SO,NR,group and &mdash;NHCOR group, and wherein Rs may be the same or different mutually, and represent a hydrogen atom, C1 to C4 alkyl group (the alkyl groups may be mutually connected to form a ring) or C1 to C4 alkylene NR&prime;,, further wherein R's represent a hydrogen atom or C1 to C4 alkyl groups which may be mutually different (the alkyl groups may be mutually connected to form a ring); and, a second additional component represented by the formula (3): CH,COCH,CONH&mdash;Z, wherein Z represents a phenyl group substituted by any one of a carboxyl group or alkali metal salts thereof, hydroxyl group or sulfonic acid group or alkali metal salts thereof, and said phenyl group may further has a substituent selected from the group consisting of a methyl group, methoxy group, chlorine atom, carboxyl group or alkali metal salts thereof, hydroxyl group or sulfonic acid group or alkali metal salts thereof. According to the method, disazo pigments can be obtained which manifest excellent transparency and flowability of the inks produced therefrom, and excellent flushing property and flushing drain coloration resistance in the pigment production process, or excellent dispersibility when ink is formed under dry condition.

Method of producing disazo pigment

A process for producing 2,5-di(arylamino)-3,6-dihydroterephthalic acid dialkyl ester having a high purity from 1,4-cyclohexanedione-2,5-di(carboxylic acid alkyl ester) at high yields for a short period of time; a process for producing quinacridone of which the byproduct content is small, from the above 2,5-di(arylamino)-3,6-dihydroterephthalic acid dialkyl ester; and a process for producing quinacridone of which the particle diameter is adjusted as desired, from the above 2,5-di(arylamino)-3,6-dihydroterephthalic acid dialkyl ester without adding a step of forming a pigment.

Process for the production of 2,5-di(arylamino)-3,6-dihydroterephthalic

A process for the production of an aromatic hydrazo compound, which comprises catalytically reducing an aromatic nitro compound with hydrogen in an alkali metal hydroxide aqueous solution and a hydrogen-donating solvent in the presence of a noble metal catalyst and a quinoid compound cocatalyst at a high temperature under a high pressure, the hydrogen-donating solvent being a cyclic hydrocarbon in which hydrogen atoms are attached to its basic skeleton having 1 to 4 aromatic rings and at least one unsaturated carbon-carbon bond remains.

Process for the production of an aromatic hydrazo compound

A process for the production of a dis-azo pigment having excellent dispersibility, high tinting strength and high masking strength, by a simple method under an improved working environment, which is improved in a drying step and can omit the pulverization step of a conventional process, the present process comprising (a) a first step of forming an aqueous paste or slurry containing a synthesized dis-azo pigment into fine particles under hot air at 100.degree. to 300.degree. C. for a short period of time within 0.5 hour, and at the same time, removing water from the formed fine particles to form a powder, and (b) a second step of keeping the powder under heat at 50.degree. to 150.degree. C. for 0.5 to 10 hours.

Process for the production of dis-azo pigment

A process for producing highly pure 6,13-dihydroquinacridone, which is a suitable intermediate for effectively producing a quinacridone pigment, for a short period of time at high yields, the process comprising providing a cylindrical reactor, providing an atmosphere free of oxygen in the cylindrical reactor, heating the cylindrical reactor so that the temperature of at least a surface of an inner wall of a cylinder of the cylindrical reactor is in the range of from 250.degree. to 400.degree. C., introducing a powder of 2,5-di(arylamino)-3,6-dihydroterephthalic acid dialkyl ester or a mixture of 2,5-di(arylamino)-3,6-dihydroterephthalic acid dialkyl ester with a liquid through a feed port provided in an upper portion of the cylindrical reactor, keeping the powder or the mixture in substantial contact with the inner wall of the cylindrical reactor so that an intramolecular alcohol-elimination reaction of the 2,5-di(arylamino)-3,6-dihydroterephthalic acid dialkyl ester takes place to form 6,13-dihydroquinacridone, and taking out the 6,13-dihydroquinacridone through an outlet provided in a lower portion of the cylindrical reactor.

Process for the production of 6,13-dihydroquinacridones and apparatus

A pigment composition which comprises a phthalocyanine pigment, a phthalocyanine derivative (A) of the formula (1),

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Tokyo, Japan

Hitoshi Maki