Abstract: A first aspect is a toner production method in which an organosilicon compound is condensed in a surfactant-containing aqueous medium with a specific surface tension, in which a resin particle is dispersed, to produce a toner having the condensate of the organosilicon compound on the surface of the resin particle, and a second aspect is a toner production method in which an organosilicon compound is condensed in an aqueous medium which has a surfactant and a specific metal salt and in which a resin particle is dispersed, to produce a toner having the condensate of the organosilicon compound on the surface of the resin particle.

Abstract: A toner including: a toner particle including a toner base particle containing a binder resin, and an organosilicon condensate present on a surface of the toner base particle, wherein a charge attenuation constant of the toner is 3.5×10?3 or more to 1.0×100 or less.

Abstract: There is provided a method of manufacturing a toner including a toner particle containing a binder resin, the method including: process 1: preparing a mixed solution including the following components i) to iii) in an aqueous medium: i) a particular silicon compound, ii) a fine particle having a number average particle diameter of 3 nm or more and 500 nm or less, and iii) a toner base particle containing the binder resin; and process 2: adjusting a pH of the mixed solution to 7.0 or more and 12.0 or less to condense the silicon compound, wherein the fine particle has an absolute value of zeta potential of 10.0 mV or more at the pH of the mixed solution of process 1.

Abstract: Provided is a toner that is excellent in development durability and has excellent solid followability even when the amount of the toner in a toner cartridge is small. The toner includes toner particles each having a surface layer containing an organosilicon polymer, in which: the organosilicon polymer includes a siloxane-based polymer having partial structures represented by the following formulae (1) and (2); and in a chart obtained by 29Si-NMR measurement of a tetrahydrofuran-insoluble matter of the toner particles, an area RT3 of a peak assigned to the partial structure represented by the following formula (1) and an area RfT3 of a peak assigned to the partial structure represented by the following formula (2) satisfy the following formula (3). 0.300>(RfT3/RT3)?0.

Abstract: Provided is a toner that is excellent in development durability and has excellent solid followability even when the amount of the toner in a toner cartridge is small. The toner includes toner particles each having a surface layer containing an organosilicon polymer, in which: the organosilicon polymer includes a siloxane-based polymer having partial structures represented by the following formulae (1) and (2); and in a chart obtained by 29Si-NMR measurement of a tetrahydrofuran-insoluble matter of the toner particles, an area RT3 of a peak assigned to the partial structure represented by the following formula (1) and an area RfT3 of a peak assigned to the partial structure represented by the following formula (2) satisfy the following formula (3). 0.300>(RfT3/RT3)?0.

Abstract: A member for electrophotography having a multilayer structure or a single-layer structure, including an outermost layer which satisfies the following A, B and C: A: the outermost layer has perfluoropolyether and a binder resin, and in the outermost layer, the ratio of the number of fluorine atoms to the number of carbon atoms is 0.10 or more and 0.40 or less; B: in a 19F-NMR spectrum of the outermost layer, the relaxation time T2 of a peak derived from CF2 moieties of perfluoropolyether is 13 milliseconds or more at 22° C.; and C: the total sum of the contents of CF3 moieties, CF2 moieties, and CF moieties in the binder resin is 5% by mass or less.

Abstract: A member for electrophotography having a multilayer structure or a single-layer structure, including an outermost layer which satisfies the following A, B and C: A: the outermost layer has perfluoropolyether and a binder resin, and in the outermost layer, the ratio of the number of fluorine atoms to the number of carbon atoms is 0.10 or more and 0.40 or less; B: in a 19F-NMR spectrum of the outermost layer, the relaxation time T2 of a peak derived from CF2 moieties of perfluoropolyether is 13 milliseconds or more at 22° C.; and C: the total sum of the contents of CF3 moieties, CF2 moieties, and CF moieties in the binder resin is 5% by mass or less.