专利摘要:
1467495 Electrophotographic toners XEROX CORP 28 Oct 1974 [2 Nov 1973] 46433/74 Heading C3P [Also in Division G2] Electrophotographic toner compositions comprise (1) an insulating polymeric material or resin and dispersed therein (2) 5 to 20 weight per cent of furnace carbon black having a surface area of 275 to 800 m.<SP>2</SP>/g., an oxygen content of 3 to 10%, a carbon black structure of 70 to 250 c.c./100 g. DBP and a particle size of 5 to 75 mÁ. The polymeric material or resin may be a polymer of an olefin, styrene, acrylate, methacrylate, acrylonitrile, vinyl chloride, vinyl carbazole, vinyl ether, vinyl ketone, vinyl alcohol or fluoroolefin, or a polyamide, polyester, polyurethane, polypeptide, polysulphide, polycarbonate, polyglycol, casein, cellulose or cellulose ester. The toners may be mixed with conventional carriers to form developers, and examples describe toners comprising furnace blacks and styrene/methyl methacrylate copolymers or polyesters, which are blended with polymer coated steel shot to form developers.
公开号:SU753368A3
申请号:SU742057006
申请日:1974-08-28
公开日:1980-07-30
发明作者:Мермельштайн Роберт;А. Критура Джон
申请人:Ксерокс Корпорейшн (Фирма);
IPC主号:
专利说明:

one
The invention relates to the field of electrography, namely to electrographic manifestation.
A known electrographic developing powder containing a pigment dispersed in resin 1.
A disadvantage of the known developing powder is its low quality.
In order to ensure the high quality of the developing powder in the proposed powder, furnace black was used as a pigment, having a specific surface of 275-300, an oxygen content of 3-10%, a structure of 70-250 cm / 100 DBP and a particle size of 5-75 µm, and its concentration is 5-20% by weight of the developing powder.
As a pigment, furnace black can be used, having a specific surface of 450-600, an oxygen content of 4-7%, a structure of 80-125 g of DBP and a particle size of 10-50 microns, and its concentration is 8-14% of the weight of the developer. powder.
As a pigment, soot furnace can also be used.
the specific surface area is 500 MVr, the oxygen content is 5.5%, the structure is 100 g of DBP and the particle size is 30 µm, and its concentration is S 12% by weight of the developer.
According to the conducted studies, in order to ensure a high quality pigment, the soot should have the following parameters - see Table 1.
Table 1
Concentration,% 5-20 8-14 12.0
The specific surface of the surface, m / g 275-800450-600 500.0
Oxygen content,% 3-10 4-75,5
Structure,
cm3 / 100 g DBP 70-250 80-125 100.0
Particle size, 30 microns5-75 10-50 30.0
The soot, named after the above parameters, is connected in a body mounted installation with a corresponding mole, as a result of which a pronounced electrographic detector with the required dielectric properties is obtained.
Particulate dyes can be taught by the kiln method, in which a cylindrical chamber is used, wiped off with a suitable flame. The camera forms a working rector. Natural gases, combusted with air in tangential inlet windows or burners, whirl, creating impact combustion at speeds of the order of 200-400 m / s (600-1200 ft / s).
A hydrocarbon or liquid oil is injected into the high velocity gas zone. Due to the fact that there is an excess of air in the combustion zone, the injection of oil leads to an increase in temperature above the level required for the decomposition of the oil into soot. The reaction products are cooled directly with a water blanket, which is several feet long. Next, the cooled product enters the normal collector equipment, where the separation of soot and its accumulation.
In combination with a carbon black dye, any suitable resin can be used, for example thermoplastics, including polyolefins such as polyethylene and polypropylene; polymers such as polybutadiene, polyisobutylene and polychloroprene; vinyl, polymers, as polytetrafluoroethylene and polyvinylide fluoride, heterocyclic thermoplastics, such as polyamides, polyesters, polypeptides, casein, polyglycols, polysul pigs and polycarbonates; cellophane, such as artificial cellulose, acetate and cellulose nitrate.
Sodium chloride, ammonium, potassium, sodium nitrate, aluminum nitrate, potassium chlorate, zirconium sand, silicon sand, methylmetaftaylate, glass, silicon dioxide, flint glass, iron, steel, ferrite, nickel, carborundum are used as the basis of the electrographic developer.
as photoconductive material can be used: sulfur, selenium, zinc sulfide, zinc oxide.
tsinkokadmievy sulfide, zinc oxide, magnesium, cadmium selenide, zinc silicate kaltsievostrontsievy sulfide, cadmium sulfide, trisulfide indium triselenid gallium disulfide, arsenic trisulfide indium triseleni gallium disulfide, arsenic trisulfide, arsenic, triselenid arsenic, antimony trisulfide , cadmium sulfoselenide and mixtures thereof.
Example 1. A control sample is obtained by using a standard xerographic developing powder, consisting of 9 weight.h, channel soot of the Neospectra type Mark t having a specific surface area of 787, oxygen content of 8% and structure of 224 g DBP, 9 weight.h. polyvinyl butyral and 82 parts by weight; styrene-2-butyl methacrylate copolymer with a 65/35 ratio by weight and a molecular weight of at least 40,000. After melting and mixing in a mixer, the composition of the pulp is rolled through the runner drum, cooled, crushed and in a fine state, it is blown through a spray in the form of colored particles (or twist), the average size of which is approximately 5-15 microns. A sample is prepared for electrical testing. For this purpose, discs are prepared by pressing at room temperature under a pressure of 5070 kg / cm2 (41200 psi). The electrical parameters of the samples are determined at a frequency of 1 kHz. The test specimens have the following operating parameters: dielectric constant 4.9; scattering coefficient 0,0170, loss factor 0,083 The developer is prepared from the developing powder described above by using 2 weight parts. it and 98 weight.h. 450 microns polymer steel spherical powder reinforcing. This formulation is kneaded for 5 minutes and placed in a standard industrial copier, in which multi-component development takes place and in which a halftone negative with a solid middle section is obtained. This method allows you to get up to 150,000 copies of good quality with a dashed area, a solid area and semitones.
The dielectric properties of the developing powder are measured using the ATM D-150-65-T program.
Example 2: A developing powder was prepared in accordance with Example 1, except that 9 weight parts were used instead of Mark II II soot. supercarbarian soot having a specific surface area of 4.6 structure 157 CMVIOO g DBP. Dielectric
the properties of this developing powder are as follows: dielectric constant 4.1; scattering coefficient 0,0110, dielectric loss coefficient 0.0450. After evaluation, it is established in the copier that only about 15-250,000 copies can be obtained, after that the copies will have traces of solid particles of the ingredient, the quality of the solid image area on the mines and halftones will dramatically increase, resulting in low-contrast and blurry images. Thus, while the usual channel black used in Example 1 gives positive results, this channel black has significant drawbacks. Consequently, not all virgieshs made of kancings have satisfactory performance.
Example 3. A developing powder was prepared in accordance with Example 1, except that 9 parts by weight of Mark II was used instead of soot from Neospectra carbon black. Pearl-L soot with a specific surface area of 135, oxygen content of 4.2%, structure 69 g DBP. The dielectric properties of this developing powder are as follows: the dielectric constant is 3.5; scattering coefficient 0,0144; dielectric loss coefficient 0,0504. The material is evaluated in a copy machine.
This developing powder only produces about 5,000 copies. Thereafter, the copies will have traces of the developing powder and will be blurred. At the same time, the quality of the solid and half-dark areas of the image decreases, resulting in blurry and low-contrast images. It is thus obvious that developing powders containing furnace soot with parameters different from those proposed in this invention will not have a satisfactory quality.
Example 4. A manufacturer is prepared from 1 weight.h. the developing powder described in Example 1 and 99 parts by weight 100 μm polymer deposited on a ferrite base. This manufacturer is placed in a conventional xerographic machine, in which the magnetic-brushing of hidden images is carried out, a document or an original is used as a test sample.
a density of 1.0 in the solid image (the machine is adjusted so that on the resulting copies it is equal to 1.00 0.05). According to the technical data of the machine, it goes to a steady mode.
after making about 1000 copies, then the next 100 copies are made. At the same time, at each tenth copy, the background or the plan is checked, which is compared with the standard series of images. The maximum background on each copy is recorded and the average of the ten measurements is taken as the average of the maximum background.
The permissible average of the maximum background or background should be less than 0.010. The lower this value, the better the quality of the developing powder. The developing powder considered in this example has an average maximum background value of 0.006. Thus, it is obvious that the developing pores with channel soot used for magnetic brushing may have satisfactory performance.
Example 5. Conducted analogously to Example 1. A manifesto is prepared from a 10 wt.h. Kiln Cszi, having a specific surface area of 525, an oxygen content of 5.0%, a structure of 105 g DBP, a particle size of 30 μm, and 90 weight parts styrene / 2-butyl-methacrylate acetate copolymer having a 65/35 weight ratio with a molecular weight of 40,000. The dielectric properties of this developing powder are as follows: dielectric constant 4.3, loss factor 0.0400. After checking on a copy machine, as described in Example 1, good copy quality (cohesive area, halftones, shading) is achieved on at least 2,000,000 copies. Thus, it is obvious that the present invention allows to obtain a developing flocker with satisfactory operating parameters, in which furnace soot is used.
Examples 6-19. Experimental developing powders consisting of styrene / p-butyl methacrylate carbon black copolymer are prepared in the same manner as described in example l.Bo in all cases, the size of soot particles should be equal to 30 microns. soot are given in table 2.
Table
Continued table. s
From these examples, it can be seen that if the penetrating powder is obtained according to the method discussed in Example 1, then the optimal dielectric properties of the reader are achieved at high concentrations of CBI and the use of carbon black with a relatively large surface area, high oxygen content and fine structure.
The background or background values given in this table are calculated as the average of 10 trials every 5000 copies obtained with each developing pig. The data show that the minimum value of the average background is obtained when the soot concentration in the bend is about 12%.
Examples 27-29, Preparative powder kits are prepared. For
Examples 2.0-26. Experimental developmental powder sets were prepared using the various amounts of carbon black required, and the properties described in Example 5.
Pa "5th characteristics about the in-. These powders are given in Table. four.
Table 4
This use 12 weight.h. furnace soot having the properties described in example 5, and 88 parts by weight corresponding polymers in the weight ratio indicated above. The average molecular weight of the copolymers ranges from 45-50,000.
The dielectric properties of the resulting powders are shown in Table. five.
The dielectric properties of the considered developing pigs were measured by the method described in example 1, the results of the evaluation of the quality of the magnetic brush development, which were determined according to example 4, are shown in the last column of the table. Thus, it is obvious that the copolymer composition also affects the image quality from the point of view of the background presence on it. Since the dielectric properties of the developing dielectric parameters of the developing powders were measured by the method described in Example 1, while the quality assessment of the magnetic alkaline manifestation was obtained according to the test program described in Example 4. s
It should be noted that the critical parameters considered in the present invention are not only for developing powders made from vinyl resins, these data can also be applied to polyester resins. While the examples given are for specific conditions and materials, any other approach may be used. In addition, the operations described in the description of the invention can be replaced, if necessary, with other h working operations.
Table 5.
This powder depends at the same time on the quality and dispersion of a certain carbon black. It is necessary to take into account in the manufacture of the powder and its viscosity in the melt,
An example is 30-32. Sets of developing powders are prepared. For this, furnace soot is used, applied on a polyester resin base, having properties according to Example 5, except for the data given in Table 6.
Table
权利要求:
Claims (2)
[1]
1. Electrographic developing powder containing pigment dispersed in a resin, characterized in that, in order to ensure high quality of development, furnace soot with a specific surface area of 275-800 MVr, oxygen content of 3-10%, structure is used as pigment 70-250 cm3 / OO g DBP and part size 5-75 µm, and its concentration is 5-20% by weight of the developing powder.
[2]
2. Powder according to claim 1, characterized in that furnace black is used as a pigment, having a specific surface of 450600, an oxygen content of 4-7%, a structure of 80-125 g DBP and a particle size of 10-50 microns, and its concentration is 8 -14% of the weight of 100 cm3 / OO g DBP and particle size
the developing powder, 30 microns, - and its concentration made 3. The powder according to claim 1, about tons of l and h and ss-12% by weight of the developing powder,
u and with the fact that as a pig-sources of information,
The furnace used soot, taken into account in the examination
having a specific surface of 500 m / g, e 1. Patent of the USSR I 499549,
oxygen content of 5.5%, structure G 03 G 9/10, published.l970.
75336814
类似技术:
公开号 | 公开日 | 专利标题
SU753368A3|1980-07-30|Electrographic developing powder
CA1129701A|1982-08-17|Carrier powder coating process
CA1068461A|1979-12-25|Magnetite electrostatographic carriers
CA1121201A|1982-04-06|Electrostatographic toner composition containinga highly fluorinated surface active additiveproviding positive triboelectric chargingpotential
JPWO2005013012A1|2006-09-28|Toner, toner manufacturing method, two-component developer, and image forming apparatus
US3895125A|1975-07-15|Process of dry development for electrophotography
US4259426A|1981-03-31|Pressure fixable microcapsule toner and electrostatic image developing method
US3969251A|1976-07-13|Developer mixture
US7090955B2|2006-08-15|Black toner, image forming method and image forming apparatus using the toner
EP0686886A1|1995-12-13|Ferrite carrier for electrophotographic developer and developer containing the carrier
US5102769A|1992-04-07|Solution coated carrier particles
JP2005284269A|2005-10-13|Toner, method for producing toner, two component developer, and image forming apparatus
US4288517A|1981-09-08|Toner for electrostatic photography containing resin coated silica particles
US3942979A|1976-03-09|Imaging system
US5314773A|1994-05-24|Black toner for electrophotography
US4963455A|1990-10-16|Developer compositions with suspension polymerized styrene butadiene resins
EP0654152B1|1996-03-20|Positively charged toner for use in electrostatography
EP0004748A2|1979-10-17|Electrostatographic developer mixture and imaging process
US20040087708A1|2004-05-06|Master batch and toner for use in electrophotography
US4164476A|1979-08-14|Developer for latent electrostatic image and process for preparation thereof
US3873325A|1975-03-25|Pressure fixable electroscopic printing powder method
JPH11174740A|1999-07-02|Carrier for developing electrostatic latent image and electrostatic charge image developer and image forming method
KR100302166B1|2001-11-14|Magnetic particles for charging, charging member, charging device, process cartridge, and electrophotographic apparatus
US4019842A|1977-04-26|Apparatus for forming magnetite electrostatographic carriers
US3883440A|1975-05-13|Liquid developer for electrophotograph
同族专利:
公开号 | 公开日
SE398926B|1978-01-23|
NL7414376A|1975-01-31|
JPS5733786B2|1982-07-19|
BE821402A|1975-02-17|
JPS5080137A|1975-06-30|
BR7407148D0|1975-08-26|
FR2250141A1|1975-05-30|
IT1025305B|1978-08-10|
CA1035988A|1978-08-08|
ES431567A1|1977-01-16|
DE2439884A1|1975-05-07|
GB1467495A|1977-03-16|
SE7413518L|1975-05-05|
DE2439884B2|1979-11-15|
FR2250141B1|1984-10-19|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题

JPH0119142B2|1980-05-19|1989-04-10|Tomoegawa Paper Mfg Ltd|
JPH0133822B2|1980-05-19|1989-07-14|Tomoegawa Paper Mfg Ltd|
WO1983002013A1|1981-11-26|1983-06-09|Kishi, Kenichi|Magnetic toner|
JPH0648399B2|1984-02-17|1994-06-22|三田工業株式会社|Method of developing electrostatic image|
DE3439482C2|1984-10-27|1993-06-09|Roehm Gmbh, 6100 Darmstadt, De|
JPS6221183U|1985-06-27|1987-02-07|
JP2769317B2|1986-06-30|1998-06-25|三田工業株式会社|Magnetic brush development|
JPS6385650A|1986-09-30|1988-04-16|Mita Ind Co Ltd|Developing method in electrophotography|
JP2596563B2|1987-09-29|1997-04-02|三田工業株式会社|Toner composition|
JP2602376B2|1991-07-17|1997-04-23|三田工業株式会社|Black toner for electrophotography|
JP2770816B2|1996-06-04|1998-07-02|ミノルタ株式会社|toner|
TWI395760B|2009-06-06|2013-05-11|Swancor Ind Co Ltd|A method of increasing the shelf life of a vinyl ester resin or an unsaturated polyester resin|
US8846283B2|2012-11-28|2014-09-30|Xerox Corporation|Hyperpigmented toner|
WO2014203811A1|2013-06-21|2014-12-24|三菱エンジニアリングプラスチックス株式会社|Crystalline thermoplastic resin composition and molded article|
EP3326224B1|2015-07-17|2019-05-08|Cabot Corporation|Oxidized carbon blacks and applications for lead acid batteries|
法律状态:
优先权:
申请号 | 申请日 | 专利标题
US41252473A| true| 1973-11-02|1973-11-02|
[返回顶部]