Technical Field
[0001] 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.
Background Art
[0002] 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.
[0003] 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.
[0004] 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.
Disclosure of the Invention
[0005] The object of the present invention is to provide a developer with its developability
little affected by the changes of temperature and process.
[0006] 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.
Most Preferred Embodiments of the Invention
[0007] 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%.
[0008] 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.
[0009] 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.
[0010] 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.
[0011] 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.
[0012] To obtain the developer of the present invention, it is preferable to use a hydrocarbon
based solvent with a volume resistivity of 10
14 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.
[0013] 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.
[0014] 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.
[0015] If the volume resistivity is less than 10
14 Ω·cm, the electrophoresis of the toner in the developer is not good, and the latent
image cannot be sufficiently developed.
[0016] The use of any solvent other than a hydrocarbon based solvent is not preferable in
view of safety, chemical stability, cost, etc.
[0017] 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.
[0018] 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.
[0019] 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.
[0020] 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.
[0021] 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.
[0022] 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.
[0023] 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.
[0024] 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.
[0025] 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.
[0026] 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%.
[0027] 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.
[0028] 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.
[0029] 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.
[0030] 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.
[0031] 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.
[0032] 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.
[0033] In addition to the above, Phthalocyanine Green, Oil Violet, Methyl Orange, Methyl
Violet, etc. are used.
[0034] 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.
[0035] Furthermore, the particles can also have a charge controlling agent, a wax, etc.
for charge control and dispersibility improvement on their surfaces.
[0036] 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.
[0037] The average particle size of the present invention is measured by using Shimadzu
Centrifugal Precipitation Type Particle Size Distribution Measuring Instrument, SA-CP3.
[0038] The viscosities of the developer and the solvent are measured by using a Brookfield
viscometer.
[0039] 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.
[0040] 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.
[0041] The image forming method of the present invention is described below.
[0042] 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.
[0043] 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.
[0044] 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.
[0045] 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.
[0046] 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.
[0047] 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.
[0048] 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.
[0049] 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.
[0050] 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.
Example 1
[0051] 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 10
18 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.
[0052] 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.
[0053] 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.
[0054] 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.
[0055] 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.
[0056] 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.
Example 2
[0057] 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.
[0058] 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%.
[0059] 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.
[0060] 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.
Example 3
[0061] 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.
[0062] 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.
[0063] 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.
[0064] 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.
Example 4
[0065] 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 10
16 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.
[0066] 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.
[0067] 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.
[0068] 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.
[0069] 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.
Comparative Example 1
[0070] 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.
[0071] 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.
Comparative Example 2
[0072] 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.
[0073] 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.
Comparative Example 3
[0074] 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.
[0075] 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.
Industrial Applicability
[0076] 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.