EP0838731A1 - Developer - Google Patents
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- Publication number
- EP0838731A1 EP0838731A1 EP96913736A EP96913736A EP0838731A1 EP 0838731 A1 EP0838731 A1 EP 0838731A1 EP 96913736 A EP96913736 A EP 96913736A EP 96913736 A EP96913736 A EP 96913736A EP 0838731 A1 EP0838731 A1 EP 0838731A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- developer
- intermediate transfer
- transfer medium
- electrostatic latent
- latent image
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
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Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/06—Developing
- G03G13/10—Developing using a liquid developer, e.g. liquid suspension
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/12—Developers with toner particles in liquid developer mixtures
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/12—Developers with toner particles in liquid developer mixtures
- G03G9/125—Developers with toner particles in liquid developer mixtures characterised by the liquid
Definitions
- the present invention relates to a developer used for copiers and laser beam printers.
- the present invention relates to a developer which is used for an image forming method containing the steps of supplying a developer onto an electrostatic latent image on an electrostatic latent image carrier by a developing roller, developing it to obtain a visible image, electrostatically transferring it in contact with an intermediate transfer medium with a silicone rubber layer on the surface, and re-transferring the transferred image on the intermediate transfer medium onto a recording medium.
- the saturation development method In the conventionally adopted saturation development method, development is effected sufficiently till the latent image charges on an electrostatic latent image carrier or electrostatic recording paper are neutralized by toner particles.
- This method has an advantage that if the electrification characteristics of the toner in the developer are controlled, a stable development density can be obtained and is little affected by the temperature change of the printer.
- the saturation development method has a problem that since it takes time for development to reach saturation, the printing speed of the printer cannot be raised.
- Japanese Patent Laid-Open (Kokai) No. 5-273865 proposes to balance the developing time and developing speed using a developing machine with a roller, for developing without reaching saturation, as a method for achieving a higher printing speed.
- the object of the present invention is to provide a developer with its developability little affected by the changes of temperature and process.
- the object can be achieved by the present invention constituted as follows.
- the present invention is a developer, in which coloring particles at least consisting of a resin and a colorant are dispersed in an insulating liquid, characterized by being 4 cst or less in the difference between the kinematic viscosity of the developer at 10°C and that at 50°C, and being 1 cst to 5 cst in kinematic viscosity at 20°C.
- coloring particles mainly consisting of a pigment and a resin are dispersed in an insulating liquid by 0.1 to 10 wt%.
- a preferable amount is 0.5 to 5 wt%.
- the amount of coloring particles dispersed is less than 0.1 wt%, the printing density becomes too low disadvantageously, and if more than 10 wt%, the white ground is contaminated disadvantageously.
- the kinematic viscosity of the developer it is preferable that the difference between the value at 10°C and that at 50°C is 4 cst or less, and more preferable is 3 cst or less. It is preferable that the kinematic viscosity at 20°C is 1 cst to 5 cst, and more preferable is 1.5 cst to 4 cst.
- the kinematic viscosity at 20°C is less than 1 cst, there occurs a problem that when the developer of the non-image area on the electrostatic latent image carrier is attempted to be mechanically removed, for example, by a roller rotating in the reverse direction, the removal efficiency is low because of the low viscosity, causing the developer to remain in the non-image area, to contaminate the white ground. If more than 5 cst, it takes a long time for development, to lower the printing speed of the printer, since the mobility of the coloring particles in the developer declines.
- the developability depends on the mobility of the toner particles in the developer in the image forming method in which the developing time and the developing speed are balanced, for example, by supplying the developer through a developing roller for development. Since the mobility depends on the viscosity of the solvent, the dependence of the kinematic viscosity on temperature results in the dependence of the development density on temperature, and such a problem occurs that the printing density of the prints is affected by temperature.
- the developer of the present invention it is preferable to use a hydrocarbon based solvent with a volume resistivity of 10 14 ⁇ cm or more as the insulating liquid. It is preferable that the solvent has a dry point of 280°C or lower in distillation and an initial boiling point of 180°C or higher, and more preferable are a dry point of 270°C or lower and an initial boiling point of 200°C or higher.
- the solvent is volatilized on the electrostatic latent image carrier to change the developer concentration at the time of the transfer to the intermediate transfer medium, thus destabilizing the transfer, in the image forming method containing the steps of supplying a developer to the electrostatic latent image on the electrostatic latent image carrier by a developing roller, developing it to obtain a visible image, electrostatically transferring it in contact with the intermediate transfer medium with a silicone rubber layer on the surface, and re-transferring the transferred image on the intermediate transfer medium onto the recording medium.
- volume resistivity is less than 10 14 ⁇ cm, the electrophoresis of the toner in the developer is not good, and the latent image cannot be sufficiently developed.
- any solvent other than a hydrocarbon based solvent is not preferable in view of safety, chemical stability, cost, etc.
- Preferable hydrocarbon based solvents include Isopar L and M (produced by Exone Kagaku K.K.), JWS-8947 (produced by Esso Sekiyu K.K.), Isozole 400 (produced by Nippon Sekiyu Kagaku K.K.), NP-LC, NP-HCS and NP-SH (produced by Mitsui Texaco Chemical K.K.), NAS-4 (produced by Nippon Oils and Fats Co., Ltd.), etc. More preferable ones are Isopar M, JWS-8947, Isozole 400, NP-LC, NP-HCS, NP-SH and NAS-4. Further more preferable ones are JWS-8947 and NP-HCS.
- the normal paraffin content of the hydrocarbon based solvent is 70 wt% or more, and more preferable is 80 wt% or more.
- the discharge electrode is liable to be contaminated in the electrophotography to uniformly electrify the electrostatic latent image carrier by corona discharge. This is considered to have relation with the problem of ozone evolution by corona discharge.
- composition of normal paraffins it is preferable that those with 12, 13 and 14 carbon atoms account for 80 wt% or more, and more preferable is 90 wt% or more.
- the normal paraffins with 12, 13 and 14 carbon atoms account for less than 80 wt%, the difference between the initial boiling point and the dry point is widened, and the balance between the stability of the transfer to the intermediate transfer medium and the transferability and fixability onto paper may be lost.
- the ultraviolet light absorbance in a wavelength range of 260 to 350 nm, of the extract obtained by extracting the hydrocarbon based solvent with dimethyl sulfoxide is 0.1 or less.
- the ultraviolet light absorbance in a wavelength range of 260 to 350 nm, of the extract obtained by extracting the hydrocarbon based solvent with dimethyl sulfoxide exceeds 0.1, the solvent is colored in long-lime running probably because of the influence of corona discharge, etc., and especially when the solvent is used for a full-color printer, etc., such a problem that colors become turbid may occur. Furthermore, a problem occurs, that an aromatic component considered as an extracted component emits an offensive odor.
- the average particle size of the coloring particles used in the present invention is 0.1 to 2.5 ⁇ m, and more preferable is 0.5 to 2 ⁇ m.
- the latent image on the electrostatic latent image carrier is pressurized. So, if the average particle size is less than 0.1 ⁇ m, the amount of the solvent existing between particles increases, and the strength of the latent image cannot withstand the pressure applied at the time of transfer, and dot tailing in the printing direction occurs. If the average particle size exceeds 2.5 ⁇ m, the particle size of the toner becomes large compared to the pixels, and the image of thin lines, etc. on the prints is coarsened.
- the coloring particles mainly contain a pigment or dye and a resin. Coloring particles with a pigment dispersed in a resin are preferable. It is preferable that the pigment content of the particles is 5 wt% to 30 wt%.
- the pigment content is less than 5 wt%, the tinting strength is insufficient, and if more than 30 wt%, the resin content becomes small, to cause insufficient fixing, lowering the gloss of the prints disadvantageously.
- the resins which can be used here include alkyd resin, styrene resin, phenol resin, acrylic resin, styrene-acrylic resin, polyester resin, rosin modified phenol resin, rosin modified maleic acid resin, etc.
- the use of rosin modified maleic acid resin is preferable.
- pigments and dyes can be used as the pigment or dye.
- Black ones include carbon black (marketed products include #30, #40, #50, MA-7, 11, 100 and 220 produced by Mitsubishi Kasei, Monarch 800, 900, Mogul L, Black Pearls 130, REGAL 330, 400 and 660R produced by Cabot, Raven 1255, 1020 and 1000 produced by Colombian Carbon, etc.), and also carbon black containing alkali blue.
- Yellow ones include C.I. Pigment Yellow - 1, 3, 4, 5, 6, 12, 13, 14, 15, 16, 17, 18, 24, 55, 65, 73, 74, 81, 83, 87, 93, 94, 95, 97, 98, 100, 101, 104, 108, 109, 110, 113, 116, 117, 120, 123, 128, 129, 133, 138, 139, 147, 151, 153, 154, 155, 156, 168, 169, 170, 171, 172 and 173.
- the use of C.I. Pigment Yellow - 12, 13, 14, 17, 81, 95, 109 and 154 is preferable.
- Red ones include C.I. Pigment Red - 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 14, 15, 17, 18, 22, 23, 31, 37, 38, 41, 42, 48 : 1, 48 : 2, 48 : 3, 48 : 4, 49 : 1, 49 : 2, 50 : 1, 52 : 1, 52 : 2, 53 : 1, 54, 57 : 1, 58 : 4, 60 : 1, 63 : 1, 63 : 2, 64 : 1, 65, 66, 67, 68, 81, 83, 88, 90, 90 : 1, 112, 114, 115, 122, 123, 133, 144, 146, 147, 149, 150, 151, 166, 168, 170, 171, 172, 174, 175, 176, 177, 178, 179, 185, 187, 188, 189, 190, 193, 194, 202, 208, 209, 214, 216, 220, 221, 224, 242, 243, 243 : 1, 245, 2
- Blue ones include C.I. Pigment Blue - 1, 2, 9, 14, 15, 16, 17 : 1, 19, 21, 22, 24, 25, 56, 60, 61, 63 and 64, and the use of C.P. Pigment Blue - 15 is preferable.
- Phthalocyanine Green, Oil Violet, Methyl Orange, Methyl Violet, etc. are used.
- the coloring particles mainly contain a pigment and a resin, and polyethylene glycol or polypropylene glycol, etc. can also be added to adjust the softening point.
- the particles can also have a charge controlling agent, a wax, etc. for charge control and dispersibility improvement on their surfaces.
- a resin and a colorant are molten and kneaded with heating using a two-screw extruder or kneader, etc. for coarse grinding, and the mixture is dispersed together with such additives as a charge controlling agent and wax in a hydrocarbon based insulating solvent using a ball mill, vibration mill or attritor, etc., to set the dispersion conditions for obtaining a predetermined particle size and particle size distribution.
- the average particle size of the present invention is measured by using Shimadzu Centrifugal Precipitation Type Particle Size Distribution Measuring Instrument, SA-CP3.
- the viscosities of the developer and the solvent are measured by using a Brookfield viscometer.
- the normal paraffin content was measured by accurately measuring 1.0 g of a sample in a 10 ml measuring flask, adding chloroform (special grade chemical, produced by Kishida Kagaku) to make a 10 ml solution, measuring the solution using Gas Chromatograph HP5890SII (produced by Hewlett Packard) with DB-1 column produced by J&W, and determining the normal paraffin content from the peak area of the peak corresponding to the standard product.
- chloroform special grade chemical, produced by Kishida Kagaku
- the ultraviolet light absorbance in a wavelength range of 260 to 350 nm, of the extract obtained by extracting the hydrocarbon solvent with dimethyl sulfoxide is measured by taking 25 ml of the hydrocarbon solvent, extracting using 5 ml of dimethyl sulfoxide for absorption spectrum, and measuring the ultraviolet light absorbance in a wavelength range of 260 to 350 nm of the extract by an ultraviolet light absorption measuring instrument.
- the developer of the present invention is used to develop an electrostatic latent image formed on an electrostatic latent image carrier, to form an image. It is preferable that the developer is used for an image forming method which contains the steps of supplying a liquid developer onto an electrostatic latent image on an electrostatic latent image carrier by a developing roller, developing it to obtain a visible image, electrostatically transferring it in contact with an intermediate transfer medium with a silicone rubber layer on the surface, and re-transferring the transformed image on the intermediate transfer medium onto a recording medium.
- an image forming method which contains the steps of supplying a liquid developer with coloring particles consisting of a resin and a colorant dispersed in an insulating liquid onto an electrostatic latent image on an electrostatic latent image carrier by a developing roller, developing it to obtain a visible image, transferring it in contact with an intermediate transfer medium with a silicone rubber layer on the surface, and re-transferring the transferred image on the intermediate transfer medium onto a recording medium, and in which the insulating liquid is removed mechanically or electrically on the electrostatic latent image carrier, to keep the solid content of the liquid developer on the electrostatic latent image carrier at 10 to 30 wt% before electrostatic transfer onto the intermediate transfer medium, characterized by being 4 cst or less in the difference between the kinematic viscosity at 10°C of the liquid developer and that at 50°C.
- the difference between the kinematic viscosity at 10°C of the liquid developer and that at 50°C is more than 4 cst, the solid content of the liquid developer on the electrostatic latent image carrier before electrostatic transfer onto the intermediate transfer medium is not kept in a range of 10 to 30 wt%, and the image trails in the printing direction to degrade the image quality.
- an image forming method which contains the steps of supplying a liquid developer to an electrostatic latent image on an electrostatic latent image carrier by a developing roller, developing it to obtain a visible image, electrostatically transferring it in contact with an intermediate transfer medium with a silicone rubber layer on the surface, re-transferring the transferred image on the intermediate transfer medium onto a recording medium, and providing a liquid removing means for removing the solvent absorbed or acting as a solvent in the silicone rubber layer of the intermediate transfer medium, characterized by using a hydrocarbon based solvent with a dry point of 280°C or lower in distillation and an initial boiling point of 180°C or higher, as the insulating liquid.
- the developer is used for an image forming method, in which a process containing the steps of supplying a liquid developer to an electrostatic latent image on an electrostatic latent image carrier by a developing roller, developing it to obtain a visible image and electrostatically transferring it in contact with an intermediate transfer medium is repeated to form a full color image on the intermediate transfer medium, and in which the full color image on the intermediate transfer medium is re-transferred onto a recording medium.
- in contact with an intermediate transfer medium means that the intermediate transfer medium and the electrostatic latent image carrier contact each other at two or more points without any development effected by the developer.
- the development by the liquid developer occurs and when the visible image is transferred, it can be considered that the intermediate transfer medium and the electrostatic latent image carrier contact each other through the toner image.
- the intermediate transfer medium of the present invention has a silicone rubber layer on a highly heat resistant rubber such as fluorine rubber through an adhesive layer, or a sponge rubber, rubber layer and silicone rubber layer laminated in this order on cloth, etc.
- the printing medium in the present invention is not limited in material, and can be any material such as paper, plastic film, metal, cloth or sheet, etc. which allows ordinary printing.
- rosin modified maleic acid resin FGM-310 produced by Arakawa Kagaku, with an acid value of 108 and a softening point of 120°C
- 400 g of carbon black (MOGUL-L) and 60 g of polyethylene glycol (PEG6000 produced by Sanyo Chemical) were preliminarily mixed by a mixer, and molten and kneaded using a two-screw extruder (at a feed rate of 2 kg/h and at 100°C).
- the obtained kneaded mixture was cooled and coarsely ground to an about 50 ⁇ m coarse powder using a sample mill.
- the developer was 2.9 cst in the kinematic viscosity at 20°C and 2.05 cst in the difference between the kinematic viscosity at 50°C and that at 10°C.
- a Se drum was used as a sensitive element, and development was effected using the obtained developer with the linear speed of the sensitive element set at 120 mm/sec.
- the toner image formed on the sensitive element was transferred onto an intermediate transfer medium stuck on a drum with silicone rubber as the outermost layer, and the toner image on the intermediate transfer medium was transferred onto art paper at a linear pressure of 20 kg with the pressure roller temperature kept at 200°C at a linear speed of 40 mm/sec.
- An image with a printing density of 1.31 free from white ground contamination could be obtained.
- Printing was carried out as described in Example 1, except that a squeeze roller rotating in the reverse direction and a charger were installed as means for removing the solvent from the developer of Example 1 on the sensitive element.
- the printer was stopped during printing and the toner on the sensitive element was collected before transfer.
- the difference of the solid content before drying and that after drying was 21.3 wt%.
- a yellow toner with an average particle size of 1.1 ⁇ m was obtained as described in Example 1, except that 400 g of C.I. Pigment Yellow-13 (Seikafast Yellow 2600 produced by Dainichi Seika) was used instead of carbon black.
- a magenta toner with an average particle size of 1.4 ⁇ m was obtained as described in Example 1, except that 400 g of C.I. Pigment Red-57 : 1 (Seikafast Carmine 6B 1476 produced by Dainichi Seika) was used instead of carbon black.
- a cyan toner with an average particle size of 0.8 ⁇ m was obtained as described in Example 1, except that 400 g of C.I. Pigment Blue - 15 (Chromofine Blue 5187 produced by Dainichi Seika) was used instead of carbon black.
- a Se drum was used as the sensitive element, and the four color developers obtained like this were used for development one after another using developing rollers with the linear speed of the sensitive element set at 120 mm/sec, and the yellow, magenta, cyan and black toners were transferred one by one onto the intermediate transfer medium stuck on a drum and with a silicone rubber as the outermost layer, to form a full color image on the intermediate transfer medium.
- the full color image was transferred onto art paper at a linear pressure of 20 kg at a pressure roll temperature of 200°C at a linear speed of 40 mm/sec.
- rosin modified maleic acid resin FGM-310 produced by Arakawa Kagaku, with an acid value of 108 and a softening point of 120°C
- 400 g of carbon black (MOGUL-L) and 60 g of polyethylene glycol (PEG 6000 produced by Sanyo Chemical) were preliminarily mixed by a mixer and molten and kneaded using a two-screw extruder (at a feed rate of 2 kg/h and 100°C).
- the obtained kneaded mixture was cooled and made into a coarse powder with a particle size of about 50 ⁇ m using a sample mill.
- the developer had a kinematic viscosity of 2.8 cst at 20°C and was 1.93 cst in the difference between the kinematic viscosity ad 50°C and that at 10°C.
- the developer was used for printing as described in Example 1, and an image with a printing density of 1.35 free from white ground contamination could be obtained.
- a liquid black toner with an average particle size of 1.2 ⁇ m and of 4.5 cst in the difference between the kinematic viscosity at 50°C and that at 10°C was produced as described in Example 1, except that Crystol 52 (produced by Esso Sekiyu) was used instead of NP-HCS.
- the toner was used for printing as described in Example 1, except that the linear speed of the pressure roller was 10 mm/sec. At room temperature 20°C, an image with a printing density of 0.85 was obtained. Printing was repeated, and when the temperature of the sensitive element reached 40°C, printing was carried out similarly. It was found that an image with a printing density of 1.23 was obtained and that the dependence of the printing density on temperature was large.
- a liquid black toner with a kinematic viscosity of 5.4 cst at 20°C and with an average particle size of 1.2 ⁇ m was produced as described in Example 1, except that Lytol White (produced by Witco) was used instead of NP-HCS.
- the toner was used for printing as described in Example 1.
- the printing density was 0.9, and to achieve the same printing density as achieved in Example 1, the linear speed of the sensitive element had to be lowered to 80 mm/sec, to lower the printing speed.
- a liquid black toner with a kinematic viscosity of 0.73 cst at 20°C and with an average particle size of 2.0 ⁇ m was produced as described in Example 1, except that Nisseki Isozol 200 (produced by Nippon Sekiyu Kagaku) was used instead of NP-HCS.
- the toner was used for printing as described in Example 1. White ground contamination showing a printing density of 0.015 occurred, and good prints could not be obtained.
- the developer of the present invention is small in the fluctuation of developability caused by the changes of temperature and process, and stable prints can be obtained at a high speed.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Liquid Developers In Electrophotography (AREA)
Abstract
A developer, in which coloring particles at least consisting of a resin and
a colorant are dispersed in an insulating liquid, characterized by being 4 cst in
the difference between the kinematic viscosity at 10°C and that at 50°C and 1
cst to 5 cst in the kinematic viscosity at 20°C.
A developer stable against the changes of temperature and process can
be obtained.
Description
The present invention relates to a developer used for copiers and laser
beam printers. Particularly, the present invention relates to a developer
which is used for an image forming method containing the steps of supplying a
developer onto an electrostatic latent image on an electrostatic latent image
carrier by a developing roller, developing it to obtain a visible image,
electrostatically transferring it in contact with an intermediate transfer
medium with a silicone rubber layer on the surface, and re-transferring the
transferred image on the intermediate transfer medium onto a recording
medium.
In the conventionally adopted saturation development method,
development is effected sufficiently till the latent image charges on an
electrostatic latent image carrier or electrostatic recording paper are
neutralized by toner particles. This method has an advantage that if the
electrification characteristics of the toner in the developer are controlled, a
stable development density can be obtained and is little affected by the
temperature change of the printer. However, the saturation development
method has a problem that since it takes time for development to reach
saturation, the printing speed of the printer cannot be raised.
To solve the problem, Japanese Patent Laid-Open (Kokai) No. 5-273865
proposes to balance the developing time and developing speed using a
developing machine with a roller, for developing without reaching saturation,
as a method for achieving a higher printing speed.
However, this method has such problems that the developing speed of
the developer is affected by the temperature change of the printer, to affect the
development density and that a higher printing speed changes the process, to
affect the development density. So, a developer stable against the changes of
temperature and process is demanded.
The object of the present invention is to provide a developer with its
developability little affected by the changes of temperature and process.
The object can be achieved by the present invention constituted as
follows. The present invention is a developer, in which coloring particles at
least consisting of a resin and a colorant are dispersed in an insulating liquid,
characterized by being 4 cst or less in the difference between the kinematic
viscosity of the developer at 10°C and that at 50°C, and being 1 cst to 5 cst in
kinematic viscosity at 20°C.
In the developer of the present invention, coloring particles mainly
consisting of a pigment and a resin are dispersed in an insulating liquid by 0.1
to 10 wt%. A preferable amount is 0.5 to 5 wt%.
If the amount of coloring particles dispersed is less than 0.1 wt%, the
printing density becomes too low disadvantageously, and if more than 10 wt%,
the white ground is contaminated disadvantageously.
As for the kinematic viscosity of the developer, it is preferable that the
difference between the value at 10°C and that at 50°C is 4 cst or less, and more
preferable is 3 cst or less. It is preferable that the kinematic viscosity at 20°C
is 1 cst to 5 cst, and more preferable is 1.5 cst to 4 cst.
If the kinematic viscosity at 20°C is less than 1 cst, there occurs a
problem that when the developer of the non-image area on the electrostatic
latent image carrier is attempted to be mechanically removed, for example, by
a roller rotating in the reverse direction, the removal efficiency is low because
of the low viscosity, causing the developer to remain in the non-image area, to
contaminate the white ground. If more than 5 cst, it takes a long time for
development, to lower the printing speed of the printer, since the mobility of
the coloring particles in the developer declines.
If the difference between the kinematic viscosity at 10°C and that at
50°C is more than 4 cst, the developability depends on the mobility of the toner
particles in the developer in the image forming method in which the
developing time and the developing speed are balanced, for example, by
supplying the developer through a developing roller for development. Since
the mobility depends on the viscosity of the solvent, the dependence of the
kinematic viscosity on temperature results in the dependence of the
development density on temperature, and such a problem occurs that the
printing density of the prints is affected by temperature.
To obtain the developer of the present invention, it is preferable to use a
hydrocarbon based solvent with a volume resistivity of 1014 Ω·cm or more as
the insulating liquid. It is preferable that the solvent has a dry point of 280°C
or lower in distillation and an initial boiling point of 180°C or higher, and more
preferable are a dry point of 270°C or lower and an initial boiling point of
200°C or higher.
If the initial boiling point in distillation is lower than 180°C, the solvent
is volatilized on the electrostatic latent image carrier to change the developer
concentration at the time of the transfer to the intermediate transfer medium,
thus destabilizing the transfer, in the image forming method containing the
steps of supplying a developer to the electrostatic latent image on the
electrostatic latent image carrier by a developing roller, developing it to obtain
a visible image, electrostatically transferring it in contact with the
intermediate transfer medium with a silicone rubber layer on the surface, and
re-transferring the transferred image on the intermediate transfer medium
onto the recording medium.
If the dry point in distillation exceeds 280°C, the energy required for
transfer from the intermediate transfer medium to paper and fixing becomes
large when the solvent is volatilized, and this is unpreferable in view of
equipment constitution.
If the volume resistivity is less than 1014 Ω·cm, the electrophoresis of
the toner in the developer is not good, and the latent image cannot be
sufficiently developed.
The use of any solvent other than a hydrocarbon based solvent is not
preferable in view of safety, chemical stability, cost, etc.
Preferable hydrocarbon based solvents include Isopar L and M (produced
by Exone Kagaku K.K.), JWS-8947 (produced by Esso Sekiyu K.K.), Isozole 400
(produced by Nippon Sekiyu Kagaku K.K.), NP-LC, NP-HCS and NP-SH
(produced by Mitsui Texaco Chemical K.K.), NAS-4 (produced by Nippon Oils
and Fats Co., Ltd.), etc. More preferable ones are Isopar M, JWS-8947, Isozole
400, NP-LC, NP-HCS, NP-SH and NAS-4. Further more preferable ones are
JWS-8947 and NP-HCS.
It is preferable that the normal paraffin content of the hydrocarbon
based solvent is 70 wt% or more, and more preferable is 80 wt% or more.
If the normal paraffin content in the hydrocarbon based solvent is less
than 70 wt%, the discharge electrode is liable to be contaminated in the
electrophotography to uniformly electrify the electrostatic latent image carrier
by corona discharge. This is considered to have relation with the problem of
ozone evolution by corona discharge.
As for the composition of normal paraffins, it is preferable that those
with 12, 13 and 14 carbon atoms account for 80 wt% or more, and more
preferable is 90 wt% or more.
If the normal paraffins with 12, 13 and 14 carbon atoms account for less
than 80 wt%, the difference between the initial boiling point and the dry point
is widened, and the balance between the stability of the transfer to the
intermediate transfer medium and the transferability and fixability onto paper
may be lost.
Furthermore, it is preferable that the ultraviolet light absorbance in a
wavelength range of 260 to 350 nm, of the extract obtained by extracting the
hydrocarbon based solvent with dimethyl sulfoxide is 0.1 or less.
If the ultraviolet light absorbance in a wavelength range of 260 to 350
nm, of the extract obtained by extracting the hydrocarbon based solvent with
dimethyl sulfoxide exceeds 0.1, the solvent is colored in long-lime running
probably because of the influence of corona discharge, etc., and especially when
the solvent is used for a full-color printer, etc., such a problem that colors
become turbid may occur. Furthermore, a problem occurs, that an aromatic
component considered as an extracted component emits an offensive odor.
It is preferable that the average particle size of the coloring particles
used in the present invention is 0.1 to 2.5 µm, and more preferable is 0.5 to 2
µm.
In the image forming method by using an intermediate transfer medium,
since the electrostatic latent image carrier and the intermediate transfer
medium contact each other when the toner is transferred from the electrostatic
latent image carrier to the intermediate transfer medium, the latent image on
the electrostatic latent image carrier is pressurized. So, if the average
particle size is less than 0.1 µm, the amount of the solvent existing between
particles increases, and the strength of the latent image cannot withstand the
pressure applied at the time of transfer, and dot tailing in the printing
direction occurs. If the average particle size exceeds 2.5 µm, the particle size
of the toner becomes large compared to the pixels, and the image of thin lines,
etc. on the prints is coarsened.
The coloring particles mainly contain a pigment or dye and a resin.
Coloring particles with a pigment dispersed in a resin are preferable. It is
preferable that the pigment content of the particles is 5 wt% to 30 wt%.
If the pigment content is less than 5 wt%, the tinting strength is
insufficient, and if more than 30 wt%, the resin content becomes small, to cause
insufficient fixing, lowering the gloss of the prints disadvantageously.
The resins which can be used here include alkyd resin, styrene resin,
phenol resin, acrylic resin, styrene-acrylic resin, polyester resin, rosin modified
phenol resin, rosin modified maleic acid resin, etc. The use of rosin modified
maleic acid resin is preferable.
As the pigment or dye, general pigments and dyes can be used. Black
ones include carbon black (marketed products include #30, #40, #50, MA-7, 11,
100 and 220 produced by Mitsubishi Kasei, Monarch 800, 900, Mogul L, Black
Pearls 130, REGAL 330, 400 and 660R produced by Cabot, Raven 1255, 1020
and 1000 produced by Colombian Carbon, etc.), and also carbon black
containing alkali blue.
Yellow ones include C.I. Pigment Yellow - 1, 3, 4, 5, 6, 12, 13, 14, 15, 16,
17, 18, 24, 55, 65, 73, 74, 81, 83, 87, 93, 94, 95, 97, 98, 100, 101, 104, 108, 109,
110, 113, 116, 117, 120, 123, 128, 129, 133, 138, 139, 147, 151, 153, 154, 155,
156, 168, 169, 170, 171, 172 and 173. The use of C.I. Pigment Yellow - 12, 13,
14, 17, 81, 95, 109 and 154 is preferable.
Red ones include C.I. Pigment Red - 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 14, 15,
17, 18, 22, 23, 31, 37, 38, 41, 42, 48 : 1, 48 : 2, 48 : 3, 48 : 4, 49 : 1, 49 : 2, 50 : 1,
52 : 1, 52 : 2, 53 : 1, 54, 57 : 1, 58 : 4, 60 : 1, 63 : 1, 63 : 2, 64 : 1, 65, 66, 67, 68, 81,
83, 88, 90, 90 : 1, 112, 114, 115, 122, 123, 133, 144, 146, 147, 149, 150, 151, 166,
168, 170, 171, 172, 174, 175, 176, 177, 178, 179, 185, 187, 188, 189, 190, 193,
194, 202, 208, 209, 214, 216, 220, 221, 224, 242, 243, 243 : 1, 245, 246 and 247.
The use of C.I. Pigment Red - 31, 48 : 3, 57 : 1, 81 and 122 is preferable.
Blue ones include C.I. Pigment Blue - 1, 2, 9, 14, 15, 16, 17 : 1, 19, 21, 22,
24, 25, 56, 60, 61, 63 and 64, and the use of C.P. Pigment Blue - 15 is
preferable.
In addition to the above, Phthalocyanine Green, Oil Violet, Methyl
Orange, Methyl Violet, etc. are used.
The coloring particles mainly contain a pigment and a resin, and
polyethylene glycol or polypropylene glycol, etc. can also be added to adjust the
softening point.
Furthermore, the particles can also have a charge controlling agent, a
wax, etc. for charge control and dispersibility improvement on their surfaces.
To produce the developer of the present invention, a resin and a colorant
are molten and kneaded with heating using a two-screw extruder or kneader,
etc. for coarse grinding, and the mixture is dispersed together with such
additives as a charge controlling agent and wax in a hydrocarbon based
insulating solvent using a ball mill, vibration mill or attritor, etc., to set the
dispersion conditions for obtaining a predetermined particle size and particle
size distribution.
The average particle size of the present invention is measured by using
Shimadzu Centrifugal Precipitation Type Particle Size Distribution Measuring
Instrument, SA-CP3.
The viscosities of the developer and the solvent are measured by using a
Brookfield viscometer.
The normal paraffin content was measured by accurately measuring 1.0
g of a sample in a 10 ml measuring flask, adding chloroform (special grade
chemical, produced by Kishida Kagaku) to make a 10 ml solution, measuring
the solution using Gas Chromatograph HP5890SII (produced by Hewlett
Packard) with DB-1 column produced by J&W, and determining the normal
paraffin content from the peak area of the peak corresponding to the standard
product.
The ultraviolet light absorbance in a wavelength range of 260 to 350 nm,
of the extract obtained by extracting the hydrocarbon solvent with dimethyl
sulfoxide is measured by taking 25 ml of the hydrocarbon solvent, extracting
using 5 ml of dimethyl sulfoxide for absorption spectrum, and measuring the
ultraviolet light absorbance in a wavelength range of 260 to 350 nm of the
extract by an ultraviolet light absorption measuring instrument.
The image forming method of the present invention is described below.
The developer of the present invention is used to develop an electrostatic
latent image formed on an electrostatic latent image carrier, to form an image.
It is preferable that the developer is used for an image forming method which
contains the steps of supplying a liquid developer onto an electrostatic latent
image on an electrostatic latent image carrier by a developing roller,
developing it to obtain a visible image, electrostatically transferring it in
contact with an intermediate transfer medium with a silicone rubber layer on
the surface, and re-transferring the transformed image on the intermediate
transfer medium onto a recording medium.
For development stable against temperature and process, preferable is
an image forming method which contains the steps of supplying a liquid
developer with coloring particles consisting of a resin and a colorant dispersed
in an insulating liquid onto an electrostatic latent image on an electrostatic
latent image carrier by a developing roller, developing it to obtain a visible
image, transferring it in contact with an intermediate transfer medium with a
silicone rubber layer on the surface, and re-transferring the transferred image
on the intermediate transfer medium onto a recording medium, and in which
the insulating liquid is removed mechanically or electrically on the
electrostatic latent image carrier, to keep the solid content of the liquid
developer on the electrostatic latent image carrier at 10 to 30 wt% before
electrostatic transfer onto the intermediate transfer medium, characterized by
being 4 cst or less in the difference between the kinematic viscosity at 10°C of
the liquid developer and that at 50°C.
If the difference between the kinematic viscosity at 10°C of the liquid
developer and that at 50°C is more than 4 cst, the solid content of the liquid
developer on the electrostatic latent image carrier before electrostatic transfer
onto the intermediate transfer medium is not kept in a range of 10 to 30 wt%,
and the image trails in the printing direction to degrade the image quality.
Furthermore, for development stable against temperature and process,
preferable is an image forming method which contains the steps of supplying a
liquid developer to an electrostatic latent image on an electrostatic latent
image carrier by a developing roller, developing it to obtain a visible image,
electrostatically transferring it in contact with an intermediate transfer
medium with a silicone rubber layer on the surface, re-transferring the
transferred image on the intermediate transfer medium onto a recording
medium, and providing a liquid removing means for removing the solvent
absorbed or acting as a solvent in the silicone rubber layer of the intermediate
transfer medium, characterized by using a hydrocarbon based solvent with a
dry point of 280°C or lower in distillation and an initial boiling point of 180°C
or higher, as the insulating liquid.
If the dry point in distillation exceeds 280°C, it is difficult to remove the
solvent absorbed or acting as a solvent in the silicone rubber layer of the
intermediate transfer medium, and a larger apparatus is required. If the
solvent is accumulated in the silicone rubber layer, the force required for
separating paper from the intermediate transfer medium becomes large, and
paper jam, etc. occur.
Furthermore, it is also preferable that the developer is used for an image
forming method, in which a process containing the steps of supplying a liquid
developer to an electrostatic latent image on an electrostatic latent image
carrier by a developing roller, developing it to obtain a visible image and
electrostatically transferring it in contact with an intermediate transfer
medium is repeated to form a full color image on the intermediate transfer
medium, and in which the full color image on the intermediate transfer
medium is re-transferred onto a recording medium.
In the above description, "in contact with an intermediate transfer
medium" means that the intermediate transfer medium and the electrostatic
latent image carrier contact each other at two or more points without any
development effected by the developer. When the development by the liquid
developer occurs and when the visible image is transferred, it can be
considered that the intermediate transfer medium and the electrostatic latent
image carrier contact each other through the toner image.
The intermediate transfer medium of the present invention has a
silicone rubber layer on a highly heat resistant rubber such as fluorine rubber
through an adhesive layer, or a sponge rubber, rubber layer and silicone rubber
layer laminated in this order on cloth, etc.
The printing medium in the present invention is not limited in material,
and can be any material such as paper, plastic film, metal, cloth or sheet, etc.
which allows ordinary printing.
One thousand five hundred and forty grams of rosin modified maleic acid
resin (FGM-310 produced by Arakawa Kagaku, with an acid value of 108 and a
softening point of 120°C), 400 g of carbon black (MOGUL-L) and 60 g of
polyethylene glycol (PEG6000 produced by Sanyo Chemical) were
preliminarily mixed by a mixer, and molten and kneaded using a two-screw
extruder (at a feed rate of 2 kg/h and at 100°C). The obtained kneaded
mixture was cooled and coarsely ground to an about 50 µm coarse powder using
a sample mill. Two hundred grams of the coarse powder, 110 g of an acrylic
high polymer type charge controlling agent solution (14 wt% in solid content,
produced according to the method described in Example XI of US Patent No.
3900412), 15 g of carnauba wax and 1250 g of petroleum hydrocarbon based
solvent NP-HCS with the following properties (produced by Mitsui Texaco
Chemical, with a volume resistivity of 1018 Ω·cm or more, initial boiling point
of 220°C, dry point of 260°C, normal paraffin content of 98.7 wt%, and
ultraviolet light absorbance peak value of 0.04 (wavelength 260 nm) in a
wavelength range of 260 to 350 nm, of the extract obtained by extracting the
hydrocarbon solvent with dimethyl sulfoxide) were mixed and ground by a
vibration mill for 5 hours, to obtain a liquid toner with an average particle size
of 1.5 µm. The raw solution was diluted by solvent NP-HCS, to have a solid
content of 2 wt%, producing a developer.
The developer was 2.9 cst in the kinematic viscosity at 20°C and 2.05 cst
in the difference between the kinematic viscosity at 50°C and that at 10°C.
At a room temperature of 20°C, a Se drum was used as a sensitive
element, and development was effected using the obtained developer with the
linear speed of the sensitive element set at 120 mm/sec. The toner image
formed on the sensitive element was transferred onto an intermediate transfer
medium stuck on a drum with silicone rubber as the outermost layer, and the
toner image on the intermediate transfer medium was transferred onto art
paper at a linear pressure of 20 kg with the pressure roller temperature kept at
200°C at a linear speed of 40 mm/sec. An image with a printing density of
1.31 free from white ground contamination could be obtained.
After transfer onto the paper, a 200°C metallic roller was kept in contact
with the intermediate transfer medium, to remove the solvent absorbed or
acting as a solvent in the silicone rubber layer.
With the room temperature raised to 30°C, printing was repeated, and
when the temperature of the sensitive element reached 40°C, printing was
effected similarly. An image with a printing density of 1.41 free from white
ground contamination could be obtained. The prints were expanded by a
microscope and examined and it was found that a good image free from dot
tailing with 30 µm smooth thin lines reproduced without being coarsened could
be obtained, and that the prints were not greatly affected by temperature.
In succession, 200 sheets were printed. The change of the printing
density could be kept within 0.2, and good prints could be obtained with good
reproducibility without any problem such as paper jam.
Printing was carried out as described in Example 1, except that a
squeeze roller rotating in the reverse direction and a charger were installed as
means for removing the solvent from the developer of Example 1 on the
sensitive element.
To measure the solid content of the developer on the electrostatic latent
image carrier before electrostatic transfer onto the intermediate transfer
medium, the printer was stopped during printing and the toner on the sensitive
element was collected before transfer. The difference of the solid content
before drying and that after drying was 21.3 wt%.
As a result, an image with a printing density of 1.28 free from white
ground contamination could be obtained. The prints were expanded by a
microscope and examined, and it was found that a good image free from dot
tailing with 30 µm smooth thin lines not coarsened could be obtained, and that
the prints were not greatly affected by temperature.
In succession, 200 sheets were printed. The change of printing density
could be kept within 0.13, and good prints could be obtained with good
reproducibility.
A yellow toner with an average particle size of 1.1 µm was obtained as
described in Example 1, except that 400 g of C.I. Pigment Yellow-13 (Seikafast
Yellow 2600 produced by Dainichi Seika) was used instead of carbon black.
A magenta toner with an average particle size of 1.4 µm was obtained as
described in Example 1, except that 400 g of C.I. Pigment Red-57 : 1 (Seikafast
Carmine 6B 1476 produced by Dainichi Seika) was used instead of carbon
black.
A cyan toner with an average particle size of 0.8 µm was obtained as
described in Example 1, except that 400 g of C.I. Pigment Blue - 15
(Chromofine Blue 5187 produced by Dainichi Seika) was used instead of carbon
black.
At room temperature 20°C, a Se drum was used as the sensitive element,
and the four color developers obtained like this were used for development one
after another using developing rollers with the linear speed of the sensitive
element set at 120 mm/sec, and the yellow, magenta, cyan and black toners
were transferred one by one onto the intermediate transfer medium stuck on a
drum and with a silicone rubber as the outermost layer, to form a full color
image on the intermediate transfer medium. The full color image was
transferred onto art paper at a linear pressure of 20 kg at a pressure roll
temperature of 200°C at a linear speed of 40 mm/sec. As a result, a good
image with a yellow printing density of 1.3, magenta printing density of 1.3,
cyan printing density of 1.5 and black printing density of 1.4 and free from
white ground contamination could be obtained. Furthermore, 500 sheets were
continuously printed, and as a result, it was found that the change of the
printing density could be kept within 0.2, and that the color superimposition
could be reproduced well.
One thousand five hundred and forty grams of rosin modified maleic acid
resin (FGM-310 produced by Arakawa Kagaku, with an acid value of 108 and a
softening point of 120°C), 400 g of carbon black (MOGUL-L) and 60 g of
polyethylene glycol (PEG 6000 produced by Sanyo Chemical) were
preliminarily mixed by a mixer and molten and kneaded using a two-screw
extruder (at a feed rate of 2 kg/h and 100°C). The obtained kneaded mixture
was cooled and made into a coarse powder with a particle size of about 50 µm
using a sample mill. Two hundred grams of the coarse powder, 110 g of an
acrylic high polymer type charge controlling agent solution (with a solid
content of 14 wt%, produced according to the method described in Example XI
of US Patent No. 3900412), 15 g of carnauba wax and 1250 g of petroleum
hydrocarbon based solvent JWS8947 with the following properties (produced
by Esso Sekiyu: with a volume resistivity of 1016 Ω·cm or more, initial boiling
point of 225°C, dry point of 242°C, normal paraffin content of 99.8 wt%, with
the amount of normal paraffins with 12, 13 and 14 carbon atoms accounting for
99.9 wt% in all the normal paraffins, and of 0.03 (wavelength 260 nm) in the
ultraviolet light absorbance peak value in a wavelength range of 260 to 350 nm,
of the extract obtained by extracting the hydrocarbon based solvent with
dimethyl sulfoxide) were mixed, and ground by a vibration mill for 5 hours, to
obtain a liquid toner with an average particle size of 1.5 µm. The raw solution
was diluted by solvent JWS8947 to achieve a solid content of 2 wt%, producing
a developer.
The developer had a kinematic viscosity of 2.8 cst at 20°C and was 1.93
cst in the difference between the kinematic viscosity ad 50°C and that at 10°C.
The developer was used for printing as described in Example 1, and an
image with a printing density of 1.35 free from white ground contamination
could be obtained.
With the room temperature raised to 30°C, printing was repeated, and
when the temperature of the sensitive element reached 40°C, printing was
carried out similarly, to obtain an image with a printing density of 1.42 free
from white ground contamination. The prints were expanded by a microscope
and examined, and it was found that an image free from dot tailing and with 30
µm smooth thin lines not coarsened could be obtained, and that the prints were
not greatly affected by temperature.
In succession, 200 sheets were printed. The change of the printing
density could be kept within 0.16, and good prints could be obtained with good
reproducibility.
A liquid black toner with an average particle size of 1.2 µm and of 4.5 cst
in the difference between the kinematic viscosity at 50°C and that at 10°C was
produced as described in Example 1, except that Crystol 52 (produced by Esso
Sekiyu) was used instead of NP-HCS.
The toner was used for printing as described in Example 1, except that
the linear speed of the pressure roller was 10 mm/sec. At room temperature
20°C, an image with a printing density of 0.85 was obtained. Printing was
repeated, and when the temperature of the sensitive element reached 40°C,
printing was carried out similarly. It was found that an image with a printing
density of 1.23 was obtained and that the dependence of the printing density on
temperature was large.
A liquid black toner with a kinematic viscosity of 5.4 cst at 20°C and with
an average particle size of 1.2 µm was produced as described in Example 1,
except that Lytol White (produced by Witco) was used instead of NP-HCS.
The toner was used for printing as described in Example 1. At room
temperature 20°C, the printing density was 0.9, and to achieve the same
printing density as achieved in Example 1, the linear speed of the sensitive
element had to be lowered to 80 mm/sec, to lower the printing speed.
A liquid black toner with a kinematic viscosity of 0.73 cst at 20°C and
with an average particle size of 2.0 µm was produced as described in Example 1,
except that Nisseki Isozol 200 (produced by Nippon Sekiyu Kagaku) was used
instead of NP-HCS.
The toner was used for printing as described in Example 1. White
ground contamination showing a printing density of 0.015 occurred, and good
prints could not be obtained.
The developer of the present invention is small in the fluctuation of
developability caused by the changes of temperature and process, and stable
prints can be obtained at a high speed.
Claims (9)
- A developer, in which coloring particles at least comprising a resin and a colorant are dispersed in an insulating liquid, characterized by being 4 cst or less in the difference between the kinematic viscosity at 10°C and that at 50°C and 1 cst to 5 cst in the kinematic viscosity at 20°C.
- A developer, according to claim 1, wherein coloring particles at least comprising a resin and a colorant are dispersed in an insulating liquid, wherein the insulating liquid is a hydrocarbon based solvent with a dry point of 280°C or lower in distillation and an initial boiling point of 180°C or higher.
- A developer, according to claim 2, wherein the insulating liquid is a hydrocarbon based solvent with a dry point of 270°C or lower in distillation and with an initial boiling point of 200°C or higher.
- A developer, according to claim 1 or 2, wherein the insulating liquid is a hydrocarbon based solvent, and the normal paraffin content in the hydrocarbon based solvent is 70 wt% or more.
- A developer, according to claim 4, wherein normal paraffins with 12, 13 and 14 carbon atoms account for 80 wt% or more in all the normal paraffins of the insulating liquid.
- A developer, according to claim 1 or 2, wherein the insulating liquid is a hydrocarbon based solvent, and the ultraviolet light absorbance in a wavelength range of 260 to 350 nm, of the extract obtained by extracting the hydrocarbon based solvent with dimethyl sulfoxide is 0.1 or less.
- A developer, according to claim 1 or 2, which is used for an image forming method containing the steps of supplying a developer onto an electrostatic latent image on an electrostatic latent image carrier, developing it to obtain a visible image, electrostatically transferring it in contact with an intermediate transfer medium with a silicone rubber layer on the surface, and re-transferring the transferred image on the intermediate transfer medium onto a printing medium.
- An image forming method which contains the steps of supplying a liquid developer onto an electrostatic latent image on an electrostatic latent image carrier, developing it for obtaining a visible image, electrostatically transferring it in contact with an intermediate transfer medium with a silicone rubber layer on the surface, and re-transferring the transferred image on the intermediate transfer medium onto a printing medium, and in which the insulating liquid is mechanically or electrically removed from the liquid developer on the electrostatic latent image carrier, to keep the solid content of the liquid developer at 10 to 30 wt% on the electrostatic latent image carrier before electrostatic transfer onto the intermediate transfer medium, characterized by being 4 cst or less in the difference between the kinematic viscosity at 10°C and that at 50°C.
- An image forming method which contains the steps of supplying a liquid developer onto an electrostatic latent image on an electrostatic latent image carrier, developing it for obtaining a visible image, electrostatically transferring it in contact with an intermediate transfer medium with a silicone rubber layer on the surface, re-transferring the transferred image on the intermediate transfer medium onto a printing medium, and providing a liquid removal means for removing the solvent absorbed or acting as a solvent in the silicone rubber layer of the intermediate transfer medium, characterized by using a hydrocarbon based solvent with a dry point of 280°C or lower in distillation and with an initial boiling point of 180°C or higher, as the insulating liquid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP1996/001257 WO1997043697A1 (en) | 1996-05-13 | 1996-05-13 | Developer |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0838731A1 true EP0838731A1 (en) | 1998-04-29 |
Family
ID=14153267
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP96913736A Withdrawn EP0838731A1 (en) | 1996-05-13 | 1996-05-13 | Developer |
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EP (1) | EP0838731A1 (en) |
KR (1) | KR19990028919A (en) |
WO (1) | WO1997043697A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2390726A1 (en) * | 2010-05-27 | 2011-11-30 | Kyocera Mita Corporation | Liquid developer, liquid developing device, and wet image forming method |
EP3343297A4 (en) * | 2015-08-27 | 2019-03-20 | Kao Corporation | Liquid developer |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
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JP5840038B2 (en) * | 2012-03-14 | 2016-01-06 | 花王株式会社 | Liquid developer |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6015063B2 (en) * | 1976-10-26 | 1985-04-17 | オーリン ハント スペシャルティ プロダクツ インコーポレイテッド | Mixed liquid toner for electrophotography |
JPH0219168U (en) * | 1988-07-25 | 1990-02-08 | ||
JPH05273865A (en) * | 1992-03-25 | 1993-10-22 | Toray Ind Inc | Electrophotographic printer |
JPH07175345A (en) * | 1993-02-03 | 1995-07-14 | Toray Ind Inc | Intermediate transfer body and image forming method using that |
-
1996
- 1996-05-13 WO PCT/JP1996/001257 patent/WO1997043697A1/en not_active Application Discontinuation
- 1996-05-13 KR KR1019980700221A patent/KR19990028919A/en not_active Application Discontinuation
- 1996-05-13 EP EP96913736A patent/EP0838731A1/en not_active Withdrawn
Non-Patent Citations (1)
Title |
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See references of WO9743697A1 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2390726A1 (en) * | 2010-05-27 | 2011-11-30 | Kyocera Mita Corporation | Liquid developer, liquid developing device, and wet image forming method |
US8846286B2 (en) | 2010-05-27 | 2014-09-30 | Kyocera Mita Corporation | Liquid developer, liquid developing device, and wet image forming method |
EP3343297A4 (en) * | 2015-08-27 | 2019-03-20 | Kao Corporation | Liquid developer |
US10261433B2 (en) | 2015-08-27 | 2019-04-16 | Kao Corporation | Liquid developer |
Also Published As
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KR19990028919A (en) | 1999-04-15 |
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