Toner for developing electrostatic latent image
An electrostatic latent image and toner technology, which is applied in the directions of developer, electrography, optics, etc., can solve the problems of particles not easy to peel off, poor image, etc., and achieve the effects of not easy to bad image, good transfer and cleaning
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[0062] [Preparation method of toner for developing electrostatic latent image]
[0063] The toner for developing electrostatic latent images of the present invention can be prepared as follows: after mixing components such as a colorant, a release agent, a charge control agent, and a magnetic powder in a binder resin, a toner mother particle of a desired particle size is prepared to make The external additive adheres to the surface of the obtained toner base particles.
[0064] In the method of preparing toner by blending components such as colorant, release agent, charge control agent, magnetic powder, etc. into the binder resin, if the resulting toner has a particle size of 3 μm or more and less than 10 μm, If the average aspect ratio is 0.820 or more and 0.900 or less, and the average aspect ratio Dn (n is an integer of 3 or more and 9 or less) of the average aspect ratio Dn of particles with a particle size of n μm or more and less than n + 1 μm, the difference between the maxi...
Embodiment
[0100] The following examples illustrate the present invention in more detail. Moreover, the present invention is not limited by the embodiment.
preparation example 1
[0103] 1960 g of propylene oxide adduct of bisphenol A, 780 g of ethylene oxide adduct of bisphenol A, 257 g of dodecenyl succinic anhydride, 770 g of terephthalic acid and 4 g of dibutyl tin oxide were added to the reaction In the container. Next, the inside of the reaction vessel was made into a nitrogen atmosphere, and the inside of the reaction vessel was heated to 235°C while stirring. Next, after performing the reaction at this temperature for 8 hours, the pressure in the reaction vessel was reduced to 8.3 kPa, and the reaction was performed for 1 hour. Then, the reaction mixture was cooled to 180°C, and trimellitic anhydride was added to the reaction vessel to form the desired oxidation. Next, the temperature of the reaction mixture was increased to 210°C at a rate of 10°C / hour, and the reaction was carried out at this temperature. After the reaction, the contents of the reaction vessel were taken out and cooled to obtain a polyester resin.
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