A method of producing a toner including the steps of: mixing resin fine particles, an organic solvent, and a resin R with a dispersion medium containing carbon dioxide, to prepare a dispersion of resin R-containing droplets; and removing the organic solvent by flowing carbon dioxide, wherein the resin fine particles contain one or more resins that have a partial structure A, B, and C, and are soluble in chloroform; the SP value of the partial structure A, the resin R, and the partial structure B satisfy particular relationships; a resin A constituted of the partial structure A and a resin B constituted of the partial structure B are soluble in the organic solvent; and a resin C constituted of the partial structure C is insoluble in the organic solvent.

The present invention relates to a water-based ink that contains pigment-containing polyester-based resin particles A, pigment-free polyester-based resin particles B, an organic solvent and water, in which a content of an organic solvent C having a boiling point of not higher than 235 C. in a whole amount of the organic solvent is not less than 90% by mass. The water-based ink of the present invention can be improved in rub fastness, solvent resistance and adhesion to a non-water absorbing printing medium with good balance therebetween, even when printed on the non-water absorbing printing medium.

The present invention relates to a water-based ink that contains pigment-containing polyester-based resin particles A, pigment-free polyester-based resin particles B, an organic solvent and water, in which a content of an organic solvent C having a boiling point of not higher than 235 C. in a whole amount of the organic solvent is not less than 90% by mass. The water-based ink of the present invention can be improved in rub fastness, solvent resistance and adhesion to a non-water absorbing printing medium with good balance therebetween, even when printed on the non-water absorbing printing medium.

Provided is an aromatic branched polycarbonate having a predetermined repeat unit in a main chain and a branched chain, and having one or more kinds of predetermined branched structures in the main chain and the branched chain, wherein ratio of a total amount of substance of the branched structures to an amount of substance of the predetermined repeat unit is in a predetermined numeric range; and containing one or more kinds of predetermined oligomers, wherein a total mass of the oligomers is in a predetermined numeric range, and a ratio of an amount of substance of oligomers having a specific structure to a total amount of substance of the oligomers is in a predetermined numeric range.

Provided is an aromatic branched polycarbonate having a predetermined repeat unit in a main chain and a branched chain, and having one or more kinds of predetermined branched structures in the main chain and the branched chain, wherein ratio of a total amount of substance of the branched structures to an amount of substance of the predetermined repeat unit is in a predetermined numeric range; and containing one or more kinds of predetermined oligomers, wherein a total mass of the oligomers is in a predetermined numeric range, and a ratio of an amount of substance of oligomers having a specific structure to a total amount of substance of the oligomers is in a predetermined numeric range.

A toner is provided. The toner contains a polyester resin. The toner has a glass transition temperature (Tg1st) at first temperature rising of differential scanning calorimetry (DSC) of from 45 C. to 65 C. The toner includes a component insoluble in tetrahydrofuran (THF) having two glass transition temperatures (Tga1st and Tgb1st) at the first temperature rising of DSC, where Tga1st is in a range of 45 C. to 5 C. and Tgb1st is in a range of 45 C. to 70 C. The toner includes a component soluble in THF having a glass transition temperature (Tg2nd) at second temperature rising of DSC of from 40 C. to 65 C.

A toner is provided. The toner contains a polyester resin. The toner has a glass transition temperature (Tg1st) at first temperature rising of differential scanning calorimetry (DSC) of from 45 C. to 65 C. The toner includes a component insoluble in tetrahydrofuran (THF) having two glass transition temperatures (Tga1st and Tgb1st) at the first temperature rising of DSC, where Tga1st is in a range of 45 C. to 5 C. and Tgb1st is in a range of 45 C. to 70 C. The toner includes a component soluble in THF having a glass transition temperature (Tg2nd) at second temperature rising of DSC of from 40 C. to 65 C.

A method of improving flowability of polycarbonate or polyarylate includes mixing the polycarbonate or the polyarylate with a flowability improver including a polyester. The polyester is a polycondensate of monomers including a bisphenol component (B) and a dicarboxylic acid component (C) at a molar ratio satisfying (B):(C)=45:55-55:45. The polyester includes a portion derived from the bisphenol component (B) and the dicarboxylic acid component (C) in an amount of 50 mol % or more.

The present invention relates to compositions containing linear polycarbonate, branched polycarbonate and a small amount of salts of sulfonic acid, sulfonamide or sulfonimide derivatives. The invention likewise relates to the use of branched polycarbonate in a polycarbonate composition for achieving a classification according to UL94 of V-0 at a layer thickness of 2.00 mm.

An electrophotographic photoreceptor includes a conductive substrate, and a lamination type photosensitive layer disposed on the conductive substrate and including a charge generation layer and a charge transport layer, in which the charge transport layer contains a polyester resin (1) having a dicarboxylic acid unit (A) represented by Formula (A) and a diol unit (B) represented by Formula (B), and an amount of a diol represented by Formula (1) in the charge transport layer is 10 ppm or less,

##STR00001## in Formula (A), n.sup.1 represents 1, 2, or 3, n.sup.1 pieces of m.sup.1's each independently represent 0, 1, 2, 3, or 4, m.sup.1 pieces of Ra.sup.1's each independently represent an alkyl group having 1 or more and 10 or less carbon atoms, an aryl group having 6 or more and 12 or less carbon atoms, or an alkoxy group having 1 or more and 6 or less carbon atoms, in Formula (B), Rb.sup.1 and Rb.sup.2 each independently represent a hydrogen atom, an alkyl group having 1 or more and 20 or less carbon atoms, an aryl group having 6 or more and 12 or less carbon atoms, or an aralkyl group having 7 or more and 20 or less carbon atoms, Rb.sup.3, Rb.sup.4, Rb.sup.5, Rb.sup.6, Rb.sup.7, Rb.sup.8, Rb.sup.9, and Rb.sup.10 each independently represent a hydrogen atom, an alkyl group having 1 or more and 10 or less carbon atoms, an aryl group having 6 or more and 12 or less carbon atoms, an aralkyl group having 7 or more and 20 or less carbon atoms, or an alkoxy group having 1 or more and 6 or less carbon atoms, and Rb.sup.1 and Rb.sup.2 may be bonded to each other to form a cyclic alkyl group, in Formula (1), R.sup.1 and R.sup.2 each independently represent a hydrogen atom, an alkyl group having 1 or more and 20 or less carbon atoms, an aryl group having 6 or more and 12 or less carbon atoms, or an aralkyl group having 7 or more and 20 or less carbon atoms, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, R.sup.8, R.sup.9, and R.sup.10 each independently represent a hydrogen atom, an alkyl group having 1 or more and 10 or less carbon atoms, an aryl group having 6 or more and 12 or less carbon atoms, an aralkyl group having 7 or more and 20 or less carbon atoms, or an alkoxy group having 1 or more and 6 or less carbon atoms, and R.sup.1 and R.sup.2 may be bonded to each other to form a cyclic alkyl group.