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GB2222268A - Electrophotographic toner - Google Patents

Electrophotographic toner Download PDF

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Publication number
GB2222268A
GB2222268A GB8916406A GB8916406A GB2222268A GB 2222268 A GB2222268 A GB 2222268A GB 8916406 A GB8916406 A GB 8916406A GB 8916406 A GB8916406 A GB 8916406A GB 2222268 A GB2222268 A GB 2222268A
Authority
GB
United Kingdom
Prior art keywords
toner
polyalkylene
weight
particles
temperature
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.)
Granted
Application number
GB8916406A
Other versions
GB8916406D0 (en
GB2222268B (en
Inventor
Masanori Ichimura
Toru Murakami
Koichi Oyamada
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujifilm Business Innovation Corp
Original Assignee
Fuji Xerox Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Fuji Xerox Co Ltd filed Critical Fuji Xerox Co Ltd
Publication of GB8916406D0 publication Critical patent/GB8916406D0/en
Publication of GB2222268A publication Critical patent/GB2222268A/en
Application granted granted Critical
Publication of GB2222268B publication Critical patent/GB2222268B/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/087Binders for toner particles
    • G03G9/08702Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/08704Polyalkenes

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  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Physics & Mathematics (AREA)
  • Developing Agents For Electrophotography (AREA)

Description

e -, r", 2 i_ 2,' 6 8 ELECTROPEOTOGRAPHIC TONER
FIELD OF THE INVENTION
The present invention relates to a toner for developing an electrostatic latent image in electrophotography, electrostatic recording and electrostatic printing.
BACKGROUND OF THE INVENTION
In the reproduction of originals by transfer of an electrostatic image, an electrostatic latent image is formed upon a photoreceptor or an electrostatic film. Fine powder, called a toner, comprising a coloring material dispersed in a binder resin is adhered to the latent image to enable it to be seen. The resulting toner image is transferred to a transfer substrate such as paper. The transferred image is then fixed, for example, by applying heat, to thereby obtain a copy. Fixing of the toner image may be effected by solvent treatment or top coating treatment, but thermal fixing is generally employed, in which the toner image is heated to a temperature sufficient to fuse the toner onto the substrate. With the recent increase of copying speed, a so-called heat roll fixing technique is commonly used, comprising passing a substrate having a toner image formed thereon through a pair of rolls composed of a heat roll and a press roll to effect heat pressing.
The heat roll fixing is considered an extremely effective method for toner fixing because it achieves higher thermal efficiency with reduced heat dispersion to rapidly accomplish fixing as compared with other thermal f ixing methods. However, since the heat roll or press roll directly contacts the toner image, a part of the toner on the substrate may to adhere to the roll, which may cause an offset phenomenon.
The offset phenomenon has been dealt with by coating the roll surface with a releasant, such as fluorine-containing resins, and supplying an offset inhibiting liquid, such as silicone oil, to the surface of the coated roll. This countermeasure, though effective to prevent the offset phenomenon, is accompanied by disadvantages, such as requiring an additional apparatus for supplying the offset inhibiting liquid to the roll surface at a constant feed rate, oil leaks may occur, and the offset inhibiting liquid gives off an odor upon heating.
Hence, attempts have recently been made to carry out heat roll fixing without using an offset inhibiting liquid as described, e.g., in JP-B-535549 (the term IIJPB" as used herein means an "examined published Japanese 1 patent application"). Various improvements in toner particles Rr se have also been proposed for the purpose of eliminating the necessity of the offset inhibiting liquid as described, e.g., in JP-B-52-3304, JP-B-5858664, JP-A-56-154740 and JP-A-57-8549 (the term "JP-All as used herein means an 1'unexamined published Japanese patent application").
In cases where use of an offset inhibiting liquid is omitted by incorporating a polyalkylene resin in a toner composition as proposed in the conventional methods as described JP-B-52-3304, the toner_ in which the polyalkylene resin is merely incorporated shows a narrow range of temperature at which fixing is feasible (fixing latitude).
SUMMARY OF THE INVENTION
One object of the present invention is to provide a tone,r which exhibits greater fixing latitude (the term "fixing latitude" means a temperature region between a lowest fixing temperature and a hot offset temperature) than results from merely incorporating a polyalkylene resin during fixing by means of fixing rolls without supplying an offset inhibiting liquid to the roll surface. In other words, the object is to provide a toner which has a broadened fixing temperature range as a result of shifting of the upper limit (high temperature causing 3 - offset) to the higher side (i.e., the upper limit of the offset temperature is shifted to from 200 to 2500C), with the lower limit (lowest fixing temperature: the lowest fixing temperature required for satisfying a desired fixing strength, for example, having the relationship, "cold offset temperature:5 lowest fixing temperature:5 hot offset temperature") being unchanged.
It has now been found that the above object of the present invention can be accomplished by an electrophotographic toner comprising a binder resin, a coloring material and a polyalkylene, wherein the polyalkylene has an average particle volume of 0.05 pM3 or more.
BRIEF DESCRIPTION OF THE DRAWINGS
The present invention will be described by reference to t he accompanying drawing wherein:
Figure 1-(a) schematically illustrates the structure of the toner particle according to this invention; Figure 1-(b) shows a maximum horizontal length of the individual polyalkylene particles in the toner particle of Fig. 1-(a); Figure 2 is a graph of average particle volume of polyalkylene particles on the vertical axis vs. kneading resin temperature on the horizontal axis; and 4 ii, 1 Figure 3 is a graph of average particle volume of polyalkylene particles on the horizontal axis vs. heat roll temperature on the vertical axis.
DETAILED DESCRIPTION OF THE INVENTION
The terminology "average particle volume" as used throughout the specification and claims means a value calculated as described below.
Individual toner particles are embedded in an appropriate binder, e.g., an epoxy resin. One of the particles is cut nearly in the center by a diamond cutter, and the cut surface is sliced off to a thickness of about 0.1 Pm. The slice is photographed by the use of transmission electron microscope (TEM) at a magnification of 15,000. The resulting electron micrograph shows a structure as schematically illustrated in Figure 1-(a), wherein the numeral 1 indicates a toner particle; 2, binder resin; 3, coloring material; and 4, polyalkylene particles. The polyalkylene particles can be easily distinguished by contrast.
The maximum horizontal length of the individual polyalkylene particles was measured by means of an image analyzer 110mnicon 3500 Model", manufactured by Shimazu Seisakusho Ltd. An average horizontal length x is obtained from ten largest measured values xl, x2, x3 .. x10 by equation:
xl + X2 + 13 +... 110 X = Assuming the individual polyalkylene particles to be spheres, an average particle volume y of the ten polyalkylene particles per toner particle can be calculated from the equation:
Y = 413n (x/2 Measurement of the average particle volume of polyalkylene particles y is made for 10 toner particles to obtain yl, y2, y3... i1o, and the average y- can be calculated by equation:
yl+y2+y3+...ylO In the present invention, the average particle volume of the polyalkylene particles should be at least 0.05 VM3. and this value can be adjusted by controlling the temperature during kneading with a binder resin as hereinaf ter described. Preferably, the average particle volume of the polyalkylene particles is in the range of 0.05 11M3 to '50 11M3, and most preferably in the range of from 0.1 VM3 to 5 pM3.
The polyalkylenes which can be used in the present invention preferably include polyethylene having a weight 11 -1 average molecular weight (Mw) of preferably from 1,500 to 6,000 (more preferably from 2,000 to 6,000) and polypropylene having an Mw of preferably from 3,000 to 6,000 (more preferably from 4,000 to 6,000).
The polyalkylenes are used in an amount of preferably from 1 to 20 parts by weight, more preferably from 2 to 15 parts by weight and most preferably from 3 to 12 parts by weight, per 100 parts by weight of the total toner components. Suitable homopolymers and copolymers of the above polyalkylenes can be mixed with a binder resin at kneading step to prepare the toner particles.
The binder resin to be used in the present invention can be selected from among thermoplastic resins without any particular limitation. Examples of usable thermoplastic resins include homopolymers or copolymers of styrenes, e.g., styrene and chlorostyrene; monoolefins, e.g., ethylene, propylene, butylene and isobutylene; vinyl esters, e.g., vinyl acetate, vinyl propionate, vinyl benzoate, and vinyl butyrate; a-methylene aliphatic monocarboxylic acid esters, e.g., methyl acrylate, ethyl acrylate, butyl acrylate, dodecyl acrylate, octyl acrylate, phenyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, and dodecyl methacrylate; vinyl ethers, e.g., vinyl methyl ether, vinyl ethyl ether, and vinyl butyl ether; and vinyl ketones, e.g., vinyl methyl ketone, vinyl hexyl ketone, and vinyl isopropenyl ketone. Typical examples of these binder resins are polystyrene, styrene-alkyl acrylate copolymers, styrene-alkyl methacrylate copoylmers, styrene-acrylonitrile copolymers, styrene- butadiene copolymers, and styrene-maleic anhydride copolymers. In addition, resins used as polyester, polyurethane, epoxy resins, silicone resins, polyamide, and modified resins may also be preferably employed.
The coloring material which can be used in the toner typically may be selected from carbon black, Nigrosine, Aniline Blue, Charchoyl Blue, Chrome Yellow, Ultramarine Blue, du Pont Oil Red, Quinoline Yellow, Methylene blue chloride, Phthalocyanine Blue, Malachite Green oxalate, lamp black, Rose Bengale, C. I. Pigment Red 48:1, C. I. Pigment Red 122, C.I. Pigment Red 57:1, C.I. Pigment Yellow 97, C.I. Pigment Yellow 12, C. I. Pigment Blue 15:1, and C. I. Pigment Blue 15:3.
The binder resin and coloring material to be used in the present invention are not limited to the aboveenumerated examples. If desired, the toner of the present invention may further contain an internal charge control agent or a magnetic powder.
The toner of the present invention can be prepared by melt-kneading the above-described low-molecular weight 1 polyalkylene, binder resin, and coloring material at an temperature of preferably from 130 to 2500C, more preferably from 140 to 2400C and most preferably from 150 to 2300C, cooling the mixture to solidify, and then grinding the solid.
As mentioned above, the average particle volume of the polyalkylene can be adjusted to the desired value by controlling constantly the kneading temperature (i.e., preferably from 130 to 2500C, more preferably from 140 to 2400C and most preferably from 150 to 230OC) while adding a small amount of water and heating a kneading chamber.
The average particle size of the toner is generally less than about 30 pm, preferably from 3 to 20 pm and particularly preferably from 6 to 14 pm.
When the area of the toner particle surface occupied by the polyalkylene is extremely increased by the increase of the average particle volume of the polyalkylene, the flowability of the toner particles tends to be decreased. In this case, the toner particles may be coated with external particles including, for example, silica particles, hydrophobic silica particles, metal oxide particles, polyvinylidene fluoride particles, and methyl polymethacrylate particles to improve the flowability of the toner particles.
An amount of the external particles used is generally from 0.05 to 20 wt% and preferably from 0.1 to 5 wt%,, based on the toner particles, and further the most preferred external particles are silica particles and hydrophobic silica particles.
The toner according to the present invention may be used either alone as a one-component-system developer or in combination with a carrier as a two-component-system developer.
The carrier to be combined with the toner in twocomponent -sys t em developers have an average particle size of up to 500 pm and may be any of known carriers, e.g., iron, nickel, cobalt, iron oxide, ferrite, glass beads, and granular silicon. The surface of the carrier may be coated, e. g., with a fluorine-containing resin, an acrylic resin, a silicone resin, etc.
The toner according to the present invention is useful for development of an electrostatic latent image formed on a photoreceptor comprising an inorganic photoconductive material (e.g., selenium, zinc oxide, cadmium sulfide, or amorphous silicon) or an organic photoconductive material (e. g., a phthalocyanine pigment or a bisazo pigment) or an electrostatic recording material having a dielectric film, e.g., of polyethylene terephthalate. That is, an electrostatic latent image is formed on the photoreceptor through an electrophotographic process of on the electrostatic recording material by use of multistylus, and the toner is adhered to the latent image by magnetic brush development, cascade development or a like developing method to form a toner image. The toner image is transferred to a transfer material, e.g., paper, followed by fixing to obtain a copy. The toner remaining on the surface of the photoreceptor, etc. is cleaned off by various methods, such as blade cleaning, brush-cleaning, web cleaning, and roll cleaning.
The present invention is now illustrated in greater detail by way of the following Examples, but it should be understood that the present invention is not deemed to be limited thereto. In these examples, all the parts are by weight unless otherwise indicated.
EXAMPLE 1
Polypropylene (Mw: 6,000) Styrenen-n-butyl acrylate crosslinked copolymer (65/35 by weight) C.I. Pigment Red 48:1 ("Symuler 10 parts by weight Neothol Red 2BY", produced by Dai-Nippon Ink & Chemicals, Inc.) 6 parts by weight 84 parts by weight Four portions of the above components were each melt-kneaded at different resin temperature of 1400C, - 11 160Cr 1800C, and 2000C, cooled to solidify, finely ground, and then classified to obtain red particles having an average particle size of 12 pm. The kneading temperature for each portion was set by controlling the amount of water added for kneading and the heating temperature of the kneading chamber.
For each portion, to the resulting particles (100 parts) was added 0.5 part of a silica fine powder having an average particle size of 20 pm, and the mixed particles were mixed in V-type mixer (i.e., twin-cylinder mixer) for 10 minutes.
An average particle volume y of the low-molecular polypropylene particles in each of the resulting four kinds of toners was determined. Fig. 2 illustrates the plot of y against the kneading resin temperature (marked with L).
Five parts of each toner were mixed with 95 parts of a steel shot carrier to prepare a developer. Copying was carried out using a copying machine "FX-3870" manufactured by Fuji Xerox Co., Ltd., and the aboveprepared developer. The toner image was transferred to transfer paper and then fixed at varying fixing heat roll temperatures which increased from 160 to 2500C in increments of 511C. The fixing temperature at which the 1 toner was not fixed on the paper and easily rubbed off with an eraser was taken as lowest fixing temperature. The fixing temperature at which the toner was transferred to the heat roll and then transferred to the next transfer paper, i.e., the temperature causing an offset phenomenon was taken as the high offset temperature.
The lowest fixing temperature and high offset temperature were plotted against the average particle volume y of the low-molecular polyalkylene in Fig. 3 (marked with Z1). In Fig. 3, the line 1 indicates the high offset temperature, and the line 2 indicates the lowest fixing temperature.
EXAMPLE 2
Polyester resin obtained from terephthalic acid and 2,2-dimethyl-1,3propanediol (a number average molecular weight:6,000) Carbon black Polypropylene (Mw; 31000) 81 parts by weight parts by weight 9 parts by weight Portions of the above components were each kneaded at different resin temperatures of 9511Cj 10011C, 110,0C 1200C, 1800C, 2000C, and 2200C, ground, and then classified to obtain particles having an average particle size of 12 pm. A silica f ine powder was added to each - 13 portion as an external additive, and each resulting toner was mixed with a steel shot carrier in the same manner as in Example 1 to prepare a developer. Each developer was evaluated in the same manner as in Example 1, and the results obtained are shown in Fig. 3 (marked with 0 EXAMPLE 3 Styrene-n-butyl acrylate copolymer Carbon black Low-moleuclar polyethylene (Mw: 3,000) 79 parts by weight parts by weight 11 parts by weight Portions of the above components were each kneaded at different resin temperatures of 1200C, 1400C, and 16011C. A developer was prepared by using the resulting particles in the same manner as in Example 2 and evaluated in the same manner as in Example 1. The results obtained are shown in Fig. 3 (marked with Cl). '- As is apparent f rom the results shown in Fig. 3, the electrophotographic toner according to the present invention has a difference between the lowest fixing temperature and the high offset temperature, i.e., fixing latitude, of 3011C, or more under a fixing condition of using no offset inhibiting liquid. Even taking possible temperature variation of the fixing heat roll per se into I 4 consideration, the toner of the present invention proved to sufficiently withstand practical use.
While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.
- is -

Claims (5)

  1. An electrophotographic toner comprising a binder resin, a coloring material, and a polyalkylene, wherein said polyalkylene has an average particle volume of 0.05 UM3 or more.
  2. 2. The electrophotographic toner as claimed in claim 1, wherein said polyalkylene is polypropylene having a weight average molecular weight of from 3,000 to 6,000 or polyethylene having a weight average molecular weight of from 1,500 to 6,000.
  3. 3. The elect rophotog raphic toner as claimed in Claim 1, wherein said polyalkylene has an average particle volume of from 0.05 UM3 to 50 UM3.
  4. 4. The elect rophotographi c toner as claimed in claim 1, wherein said polyalkylene is used in an amount of from 1 to 20 parts by weight per 100 parts by weight of the total toner components.
  5. 5. An electrophotogra12hic toner as claimed in claim 19 substantially as hereinbefore described in any one ffif Examples 1 to 3.
    An electrophotographic toner as claimed in claim 1, substantially an hereinbefore described with reference to the accompanying drawings.
    Published 1990 atThePateritOfficp,State House. 6671 High Holborn. London WClR 4TP. Further copies maybe obtainedfrom The PatentOfftceSales Branch, St Mar7 Cray. Orpingtop. Kei-t BR5 33F.D. Prirted by TA.A.liplex techruques Ita. St, Mary Qay. Kent, Con. 1187 z
GB8916406A 1988-07-18 1989-07-18 Electrophotographic toner Expired - Lifetime GB2222268B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63176944A JPH0227363A (en) 1988-07-18 1988-07-18 Toner for electrophotography

Publications (3)

Publication Number Publication Date
GB8916406D0 GB8916406D0 (en) 1989-09-06
GB2222268A true GB2222268A (en) 1990-02-28
GB2222268B GB2222268B (en) 1992-04-22

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GB8916406A Expired - Lifetime GB2222268B (en) 1988-07-18 1989-07-18 Electrophotographic toner

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JP (1) JPH0227363A (en)
DE (1) DE3923784C2 (en)
GB (1) GB2222268B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2336442A (en) * 1998-04-17 1999-10-20 Ricoh Kk Toner

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002156775A (en) * 2000-11-21 2002-05-31 Fujitsu Ltd Color toner for flash fixing

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5147622B2 (en) * 1973-05-31 1976-12-16
JPS5219535A (en) * 1975-08-06 1977-02-14 Ricoh Co Ltd Dry type developing powder
JPS57144565A (en) * 1981-03-02 1982-09-07 Canon Inc Pressure fixable magnetic toner
JPS5945455A (en) * 1982-09-08 1984-03-14 Toshiba Corp Electrophotographic developer
US4556624A (en) * 1984-09-27 1985-12-03 Xerox Corporation Toner compositions with crosslinked resins and low molecular weight wax components
JPH0682226B2 (en) * 1985-12-17 1994-10-19 キヤノン株式会社 Image forming method
JP2504745B2 (en) * 1986-07-08 1996-06-05 三田工業株式会社 Method of manufacturing toner for electrophotography

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2336442A (en) * 1998-04-17 1999-10-20 Ricoh Kk Toner
GB2336442B (en) * 1998-04-17 2000-09-06 Ricoh Kk Multi-color toner set and method of forming multi-color images, using the multi-color toner set
US6180298B1 (en) 1998-04-17 2001-01-30 Ricoh Company, Ltd. Multi-color toner set and method of forming multi-color images, using the multi-color toner set

Also Published As

Publication number Publication date
DE3923784A1 (en) 1990-01-25
GB8916406D0 (en) 1989-09-06
DE3923784C2 (en) 1995-02-09
JPH0227363A (en) 1990-01-30
GB2222268B (en) 1992-04-22

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PCNP Patent ceased through non-payment of renewal fee

Effective date: 20000718