C09D11/033

Photocurable ink, ink container, and image forming method

A photocurable ink contains a polymerizable compound and a photopolymerization initiator, and this ink contains a low boiling point solvent having a boiling point of 40 C. to 120 C. at one atmospheric pressure and at least one particle having a surface on which an unsaturated hydrocarbon group is provided.

Photocurable ink, ink container, and image forming method

A photocurable ink contains a polymerizable compound and a photopolymerization initiator, and this ink contains a low boiling point solvent having a boiling point of 40 C. to 120 C. at one atmospheric pressure and at least one particle having a surface on which an unsaturated hydrocarbon group is provided.

THERMAL INKJET DYE SUBLIMATION INKS
20200369899 · 2020-11-26 ·

A thermal inkjet dye sublimation ink consists of a disperse dye colorant dispersion, primary and secondary solvents, a chelating agent, oleth-3-phosphate, additive(s), and water. The colorant dispersion is present in an amount ranging from about 1 wt % actives to about 7 wt % actives. The amount of the primary solvent (glycerol, ethoxylated glycerol, 2-methyl-1,3-propanediol, dipropylene glycol, or combinations thereof) ranges from about 10 wt % to about 22 wt %, and the amount of the secondary solvent ranges from 0 wt % to about 7 wt %. The chelating agent amount ranges from 0 wt % actives to less than 0.1 wt % actives, and the oleth-3-phosphate amount ranges from about 0.1 wt % to about 0.75 wt. The additive is selected from the group consisting of a buffer, a biocide, another surfactant, and combinations thereof.

THERMAL INKJET DYE SUBLIMATION INKS
20200369899 · 2020-11-26 ·

A thermal inkjet dye sublimation ink consists of a disperse dye colorant dispersion, primary and secondary solvents, a chelating agent, oleth-3-phosphate, additive(s), and water. The colorant dispersion is present in an amount ranging from about 1 wt % actives to about 7 wt % actives. The amount of the primary solvent (glycerol, ethoxylated glycerol, 2-methyl-1,3-propanediol, dipropylene glycol, or combinations thereof) ranges from about 10 wt % to about 22 wt %, and the amount of the secondary solvent ranges from 0 wt % to about 7 wt %. The chelating agent amount ranges from 0 wt % actives to less than 0.1 wt % actives, and the oleth-3-phosphate amount ranges from about 0.1 wt % to about 0.75 wt. The additive is selected from the group consisting of a buffer, a biocide, another surfactant, and combinations thereof.

LIGHT-EMITTING LAYER-FORMING INK AND MANUFACTURING METHOD OF ORGANIC EL ELEMENT

Disclosed is a light-emitting layer-forming ink useful in forming an organic light-emitting layer for an organic EL element by a printing process, including a tetralin-based organic solvent, and a solute including an anthracene-based, low molecular material and dissolved at a concentration of 3% or higher and 12% or lower in the tetralin-based organic solvent.

LIGHT-EMITTING LAYER-FORMING INK AND MANUFACTURING METHOD OF ORGANIC EL ELEMENT

Disclosed is a light-emitting layer-forming ink useful in forming an organic light-emitting layer for an organic EL element by a printing process, including a tetralin-based organic solvent, and a solute including an anthracene-based, low molecular material and dissolved at a concentration of 3% or higher and 12% or lower in the tetralin-based organic solvent.

Ink jet recording method and ink jet recording apparatus

An ink jet recording method including the steps of a first recording step for applying a first ink to a recording medium and a second recording step for applying a second ink to the recording medium so as to overlap at least a region provided with the first ink, wherein the first ink is an aqueous ink containing silver particles, the second ink is an aqueous ink containing a dye, a time difference between applications of the first ink and the second ink to the recording medium is 1 sec or more to 7,200 sec or less, and the dye is a predetermined dye.

Ink jet recording method and ink jet recording apparatus

An ink jet recording method including the steps of a first recording step for applying a first ink to a recording medium and a second recording step for applying a second ink to the recording medium so as to overlap at least a region provided with the first ink, wherein the first ink is an aqueous ink containing silver particles, the second ink is an aqueous ink containing a dye, a time difference between applications of the first ink and the second ink to the recording medium is 1 sec or more to 7,200 sec or less, and the dye is a predetermined dye.

Method for obtaining hydrocarbon solvents with boiling point above 300° C. and pour point lower than or equal to −25° C

A method for producing hydrocarbon solvents having a sulfur content of less than 10 ppm, aromatic hydrocarbon content of less than 500 ppm, an initial boiling point higher than or equal to 300 C. and final boiling point lower than or equal to 500 C., for a fraction interval of a maximum of 100 C., and pour point lower than 25 C. according to the standard ASTM D5950, comprising of the following steps of: dewaxing of a hydrocarbon fraction having initial boiling point higher than 300 C. derived from the distillation of a gas oil fraction, hydrodearomatisation of all or part of the dewaxed effluent, in the presence of a catalyst comprising nickel on an alumina base, at a pressure ranging from 60 to 200 bar and a temperature ranging from 80 C. to 250 C., recovery of the dewaxed and dearomatised fraction, distillation in fractions of the dewaxed and dearomatised fraction, recovery of at least one 300 C.+ fraction having pour point lower than 25 C., this fraction having a distillation interval lower than 100 C.

Method for obtaining hydrocarbon solvents with boiling point above 300° C. and pour point lower than or equal to −25° C

A method for producing hydrocarbon solvents having a sulfur content of less than 10 ppm, aromatic hydrocarbon content of less than 500 ppm, an initial boiling point higher than or equal to 300 C. and final boiling point lower than or equal to 500 C., for a fraction interval of a maximum of 100 C., and pour point lower than 25 C. according to the standard ASTM D5950, comprising of the following steps of: dewaxing of a hydrocarbon fraction having initial boiling point higher than 300 C. derived from the distillation of a gas oil fraction, hydrodearomatisation of all or part of the dewaxed effluent, in the presence of a catalyst comprising nickel on an alumina base, at a pressure ranging from 60 to 200 bar and a temperature ranging from 80 C. to 250 C., recovery of the dewaxed and dearomatised fraction, distillation in fractions of the dewaxed and dearomatised fraction, recovery of at least one 300 C.+ fraction having pour point lower than 25 C., this fraction having a distillation interval lower than 100 C.