WO1997005529A1 - Toner de fixation par laminage a chaud pour developper des images a charge electrostatique - Google Patents
Toner de fixation par laminage a chaud pour developper des images a charge electrostatique Download PDFInfo
- Publication number
- WO1997005529A1 WO1997005529A1 PCT/JP1996/002133 JP9602133W WO9705529A1 WO 1997005529 A1 WO1997005529 A1 WO 1997005529A1 JP 9602133 W JP9602133 W JP 9602133W WO 9705529 A1 WO9705529 A1 WO 9705529A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- toner
- resin
- weight
- cyclic structure
- polyolefin resin
- 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.)
- Ceased
Links
Classifications
-
- 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
- G03G9/087—Binders for toner particles
-
- 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
- G03G9/087—Binders for toner particles
- G03G9/08784—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
- G03G9/08797—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775 characterised by their physical properties, e.g. viscosity, solubility, melting temperature, softening temperature, glass transition temperature
-
- 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
- G03G9/087—Binders for toner particles
- G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/08704—Polyalkenes
-
- 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
- G03G9/087—Binders for toner particles
- G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/08735—Polymers of unsaturated cyclic compounds having no unsaturated aliphatic groups in a side-chain, e.g. coumarone-indene resins
-
- 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
- G03G9/087—Binders for toner particles
- G03G9/08784—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
- G03G9/08791—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775 characterised by the presence of specified groups or side chains
-
- 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
- G03G9/087—Binders for toner particles
- G03G9/08784—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
- G03G9/08793—Crosslinked polymers
Definitions
- the present invention relates to a heat roller-fixable electrostatic image developing toner, and more specifically, when fixing a dry one-component magnetic toner, a dry one-component non-magnetic toner, a dry two-component toner, and a liquid toner, a toner vent prevention effect.
- the present invention relates to a toner having excellent fixability and transparency and capable of forming a clear image. Background art
- Table 1 shows the general prescription of the toner in the fixed charge type electrostatic image developing type copier and printer.
- One of the main factors to improve the clearness, light transmittance and fixability of the copied image is shown in Table 1.
- a toner is supplied to an electrostatic image on a latent image carrier to obtain a visible image, and the toner image is converted to plain paper or black paper. ⁇ ⁇ It is transferred to a film for ⁇ and fixed.
- styrene-acrylic resin and polyester resin are often used as the binder resin.However, in the former case, the light transmittance and clarity of the toner are not sufficiently obtained, and accordingly, high-quality images are produced. In a situation where it is difficult to obtain, in the latter, light transmittance is obtained, but there is a defect in sharpness because the resin is yellowish. (Unit: wt%)
- An object of the present invention to provide a high-quality fixed-heat roller fixed-type electrostatic image developing copier and a high-quality copy image of a pudding image, that is, excellent fixability, light transmittance, and sharpness.
- An object of the present invention is to provide a toner in a dry two-component system, a dry non-magnetic one-component system, a dry magnetic one-component system, and a liquid toner developer. Disclosure of the invention
- the binder resin contains a polyolefin resin having at least a cyclic structure, i.v. (intrinsic viscosity) ⁇ 0.25 dl / g, HDT (heat distortion temperature!) IN 5 3 4 6 1 1 B) ⁇ 70 ° C and measurement by GPC
- the binder resin contains less than 50% by weight of a polyolefin resin having a cyclic structure having a number average molecular weight of 7500 or more and a weight average molecular weight of 1500 or more in the entire binder resin.
- the binder resin is composed of 1 to 100 parts by weight of a polyolefin resin having a cyclic structure, a polyester resin, an epoxy resin, a polyolefin resin, a vinyl acetate resin, a vinyl acetate copolymer resin, and styrene.
- the polyolefin resin having a cyclic structure is composed of a carboxyl group, And a heating roller fixing type toner for developing an electrostatic image as described in the above item 1 or 2, wherein the toner has at least one functional group selected from a group and an amino group.
- the polyolefin resin having a cyclic structure has a structure crosslinked by an ionomer or a gene, and the heating roller fixed attachment according to the first, second, or third aspect,
- a toner for developing an electrostatic image There is provided a toner for developing an electrostatic image.
- the present inventors have conceived, as a solution, to use a colorless and highly transparent resin in order to solve the above problems.
- examples of such a resin include polycarbonate, polyacrylate, polymer acrylate, and polystyrene. These resins are required for a binder resin, for example, fixing strength, heat response (heat response). It is not known that it is satisfactory in terms of properties, and it is already known that there is a problem in using it as a binder resin.
- the present inventors have conducted various studies to improve this disadvantage, and as a result, have found that the polyolefin resin having a cyclic structure which is colorless and transparent and has a high light transmittance, but which has a high viscosity among polyolefin resins having the cyclic structure. It has been confirmed that the use of a resin containing less than 50% by weight of the entire resin in the binder resin makes it possible to produce a toner that provides high-quality images. The present invention has been completed based on these findings.
- a toner that uses a polyolefin resin with a cyclic structure that satisfies these characteristics as a binder resin has high quality, that is, excellent fixing strength, heat response (heat response) properties, and light transmission, and realizes clear images.
- the characteristics can be exhibited in a color toner.
- the heat roller-fixable electrostatic image developing toner of the present invention is characterized in that the binder resin contains at least a polyolefin resin having a cyclic structure, and iv (intrinsic viscosity) ⁇ 0.25 d1 / g. HDT (heat distortion temperature DIN 5 3 4 6 1-B) ⁇ 70 ° C, and the number average molecular weight is more than 7500 and the weight average molecular weight is more than 1500 It is characterized in that it contains less than 50% by weight of a polyolefin resin having a certain cyclic structure in the whole binder resin.
- the polyolefin resin having a cyclic structure used here is, for example, a one-year-old olefin such as ethylene, propylene or butylene and a double olefin such as cyclohexene or norbornene. It is a copolymer with an alicyclic compound having a bond, is colorless and transparent, and has high light transmittance.
- the polyolefin having a cyclic structure is a polymer obtained by a polymerization method using, for example, a meta-mouth catalyst or a Ziegler catalyst.
- the colorless transparent polyolefin resin having a cyclic structure with high light transmittance used in the present invention has a number average molecular weight of 1,000 to 7,500, preferably 3000 to 7,500, and a weight average molecular weight of 1,000 to 1,000, as measured by the GPC method.
- the polyolefin resin having a low-viscosity cyclic structure has the number average molecular weight Mn, weight average molecular weight Mw, intrinsic viscosity iv, and heat distortion temperature (HDT), it is used as a measure of the degree of dispersion of the molecular weight distribution. Since Mw / Mn is as small as 1 to 2.5, that is, close to monodispersion, it is possible to produce a toner with high heat response and high fixing strength, which is a necessary performance as a toner.
- the characteristic of the polyolefin resin having a cyclic structure according to the present invention is that, for example, in the case of T 745 shown in Table 2 below, the azo pigment permanent rubin F 6B (manufactured by Hoechst) is used. After adding 5% and dispersing it sufficiently in a kneader, it is sheeted with a press machine, and the light transmission measured with a Macbeth densitometer RD 914 (Phil Yuichi SP I red) with visible light of 624 nm. The ratio is 12.0%, while that of styrene-acrylic resin is 7.0% and that of polyester resin is 15.5%. Has excellent transparency and can be used for color toner as well as polyester resin. In addition, the resin has a very low heat of fusion as measured by the DSC method, which can be expected to significantly reduce the energy consumption for fixing.
- the polyolefin resin having a high-viscosity cyclic structure since the polyolefin resin having a high-viscosity cyclic structure has the above-mentioned physical properties, it imparts structural viscosity to the toner as compared with the case of the low-viscosity resin, thereby increasing the viscosity. ⁇ Improves the offset prevention effect and the adhesiveness to paper and film base material.
- a polyolefin resin having a low-viscosity cyclic structure improves the melt fluidity of the toner and satisfies the toner properties that require instantaneous melting and solidification behavior.
- the amount of the high-viscosity resin used is 50% or more, the uniform kneading property is extremely reduced, which hinders the toner performance. In other words, clear images with high quality, that is, high fixing strength, and excellent thermal responsiveness cannot be obtained.
- the use ratio of the resin having a cyclic structure in the binder resin to the other resin is 1 to 100, preferably 20 to 90, more preferably 50 to 90 weight by weight of the former. Parts, the latter being from 0 to 99, preferably from 10 to 80, more preferably from 10 to 50 parts by weight. If the former is less than 1 part by weight, it will be difficult to obtain high-quality images.
- metal such as zinc, copper, calcium, etc. may be added to polyolefin resin having a cyclic structure by copolymerization with a gen monomer such as norbornadiene or cyclohexadiene, or to polyolefin resin having a cyclic structure having a carboxyl group introduced therein.
- the heat roller-fixable electrostatic image developing toner of the present invention can improve the fixability by introducing a cross-linked structure by the addition of a coloring agent, a charge controlling agent, and, if necessary, to the binder resin.
- a function-imparting agent or other additives can be added, and the composition can be obtained by a conventionally known method such as kneading, pulverization, classification, and the like. Further, a fluidizing agent and the like are added as necessary.
- coloring agent conventionally known coloring agents such as carbon black, diazoyl, phthalocyanine, quinacridone, carmine, monoazolide, and perylene can be used.
- charge control agent include a nig mouth dye, a fatty acid-modified nig mouth dye, a metal-containing nig mouth dye, a combined metal fatty acid-modified nig mouth dye, a chromium complex of 3,5-di-tert-butylsalicylic acid, Conventionally known compounds such as a quaternary ammonium salt, a triphenylmethane dye, and an azochrome complex can be used.
- a known function-imparting agent preferably a wax having a melting point of 60 to 170 ° C.
- a wax having a melting point of 60 to 170 ° C.
- examples of the wax having the above melting point include carnauba wax, montan wax, glycerin monostearate and the like.
- a fluidizing agent such as colloidal silica, aluminum oxide, and titanium oxide, and a lubricant comprising a fatty acid metal salt such as barium stearate, calcium stearate, and palladium laurate can be added to the toner of the present invention.
- the toner of the present invention can be used as a one-component developer or as a toner of a two-component developer. Further, the toner of the present invention can be used as a one-component magnetic toner by mixing magnetic powder, or can be used as a full-color toner.
- the present invention will be further described below with reference to Examples and Comparative Examples. Will be explained.
- Dry magnetic one-component system dry magnetic one-component system; magnetic powder (manufactured by Titanium Co., Ltd., BL100) 40% by weight, charge control agent (manufactured by Hoechst Co., Ltd., Kobi-Charge NX) 5% by weight, wax (manufactured by Hoechst, Hostus) Evening FE— 2) 2.5% by weight, fumed silica HDK-H 2000) 0.5% by weight, calcium carbonate (manufactured by Shiraishi Calcium Co., Ltd.) 2.0% by weight and binder resin 50% by weight, and mixed at 150 ° C with two rolls. After melt-kneading, the mixture was cooled and solidified, coarsely pulverized, then refined and classified by a jet mill, and adjusted to an average particle size of about 10 m to prepare a toner.
- charge control agent manufactured by Hoechst Co., Ltd., Kobi-Charge NX
- wax manufactured by Hoechst, Hostus
- Liquid toner carbon black (MA-7, manufactured by Mitsubishi Chemical Corporation) as a colorant, 1 part by weight, charge control agent (Hechist, reflex blue: 51) 0.5 part by weight and binder resin was mixed with 40% by weight of 98.5 parts by weight and 60% by weight of an electrolytic solution (Isson H, manufactured by Exxon) and kneaded with a sand mill to prepare a toner.
- charge control agent Hechist, reflex blue: 51
- binder resin was mixed with 40% by weight of 98.5 parts by weight and 60% by weight of an electrolytic solution (Isson H, manufactured by Exxon) and kneaded with a sand mill to prepare a toner.
- the toners of Examples 1 to 27 and Comparative Examples 1 to 6 were prepared using the toner preparation method and the binder resin shown in Table 2 below.
- Table 3 shows the basic physical properties of the polyolefin resin having the cyclic structure used and the names of other resins.
- Example 12 3 50 2-2
- Example 23 III 3 24 7 15.4
- Example 24 III 3 24 8 15.4
- Example 25 III 5 39.4
- Example 11 26
- Example 27 III 5 24 8 15.4 Comparative Example 1 I 7 87
- the toner prepared by the above toner preparation method 1 or 2 was put into a commercially available electrophotographic copying machine (PC100, manufactured by Canon Inc.) to perform a performance test.
- the toner prepared by the toner preparation method 3 was put into a commercially available electrophotographic copying machine (FT40Oi manufactured by Ricoh Company) to perform a performance test.
- Table 4 The results are summarized in Table 4.
- the copy speed and fixing temperature using the toners prepared according to the respective prescriptions were set at 10 sheets / min.1 Samples copied on recycled paper at 10 ° C intervals in the range of 10 to 140 ° C were collected by Sutherland Co., Ltd. Rubbed 10 times with an eraser using an abrasion resistance tester made by Azuma. The load at that time was 40 g / cm z . The print density of the sample was measured with a Macbeth reflection densitometer. When at least one of the measured values at each temperature was less than 65%, X, 65% or more and less than 75%, and X were 75% or more.
- magenta-toner toners prepared according to the prescriptions of Examples and Comparative Examples, sheet-shaped samples having a film thickness of 100 m were prepared.
- the light transmittance of the sheet sample was measured using a spectral filter having a peak at 624 nm.
- the transmittance at 624 nm of less than 8% was X, 8% or more and less than 11% was ⁇ , and 11% or more was ⁇ .
- a predetermined amount of the toner described in Examples and Comparative Examples and a ferrite carrier manufactured by Powder Tech Co., Ltd. are placed in a developer box, and 5 g of the toner-adhered carrier stirred and rubbed for 1 week is weighed. Put it in mineral water, remove the toner adhering to the surface by static electricity, and take out only the carrier magnetic powder by magnet. The magnetic powder is immersed in acetone to dissolve and remove the surface-fused Svent toner, and the change in weight before and after the immersion treatment is 0.2% or less for ⁇ , 0.2 to 0.5% for ⁇ , 0.5 % Or more was defined as X.
- the toner for developing an electrostatic charge image with a hot-opener fixing type contains a polyolefin resin having at least a cyclic structure as a binder resin, and has a high viscosity of the above-mentioned polyolefin resin.
- ⁇ ⁇ ⁇ Since the fin resin content is less than 50% by weight in the whole binder resin, it has excellent fixability, light transmittance and toner spent resistance, and obtains clear high quality images. And its characteristics are exhibited particularly when used in a color toner.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Developing Agents For Electrophotography (AREA)
Description
Claims
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE69632732T DE69632732T2 (de) | 1995-08-02 | 1996-07-29 | Heizwalzen-wärmefixierbare toner für die entwicklung elektrostatisch geladener bilder |
| CA002228506A CA2228506C (en) | 1995-08-02 | 1996-07-29 | Toner for developing electrostatically charged image of heat roller type copier or printer |
| US09/000,330 US7252918B2 (en) | 1995-08-02 | 1996-07-29 | Hot-roller fixing toner for developing electrostatically charged images |
| EP96925122A EP0843223B1 (en) | 1995-08-02 | 1996-07-29 | Hot-roller fixing toner for developing electrostatically charged images |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7/216751 | 1995-08-02 | ||
| JP21675195 | 1995-08-02 | ||
| JP7/354063 | 1995-12-29 | ||
| JP35406395A JP3274052B2 (ja) | 1995-08-02 | 1995-12-29 | 加熱ローラー定着型静電荷像現像用トナー |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1997005529A1 true WO1997005529A1 (fr) | 1997-02-13 |
Family
ID=26521605
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP1996/002133 Ceased WO1997005529A1 (fr) | 1995-08-02 | 1996-07-29 | Toner de fixation par laminage a chaud pour developper des images a charge electrostatique |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7252918B2 (ja) |
| EP (1) | EP0843223B1 (ja) |
| JP (1) | JP3274052B2 (ja) |
| KR (1) | KR100439513B1 (ja) |
| CN (1) | CN1130603C (ja) |
| DE (1) | DE69632732T2 (ja) |
| ES (1) | ES2222482T3 (ja) |
| TW (1) | TW509827B (ja) |
| WO (1) | WO1997005529A1 (ja) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7049040B2 (en) * | 1996-12-26 | 2006-05-23 | Ticona Gmbh | Electrostatically charged image developing toner containing a polyolefin resin having a cyclic structure |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0943891A (ja) * | 1995-08-02 | 1997-02-14 | Hoechst Ind Kk | 電子写真用トナー |
| JPH09185185A (ja) * | 1995-12-29 | 1997-07-15 | Hoechst Ind Kk | 静電荷像現像用コートキャリア |
| JP4174105B2 (ja) | 1998-08-20 | 2008-10-29 | ティコナ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 静電荷像現像用トナー |
| JP3434218B2 (ja) * | 1998-11-02 | 2003-08-04 | ティコナ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 静電荷像現像用トナー |
| JP3449935B2 (ja) * | 1999-01-11 | 2003-09-22 | 株式会社巴川製紙所 | 電子写真用乾式トナー |
| DE19929809A1 (de) | 1999-06-30 | 2001-01-04 | Ticona Gmbh | Kontinuierliches Verfahren zur Herstellung eines amorphen Polyolefins mit breiter Molmassenverteilung und einheitlicher Glastemperatur |
| DE60229330D1 (de) | 2001-07-23 | 2008-11-27 | Ricoh Kk | Ölfreier Toner |
| JP3863744B2 (ja) | 2001-08-31 | 2006-12-27 | 株式会社巴川製紙所 | リサイクルシステム用トナー及びそれを用いたトナーリサイクル式現像方法 |
| JP3880359B2 (ja) | 2001-10-05 | 2007-02-14 | 株式会社巴川製紙所 | オイルレス定着用フルカラートナー |
| JP3942520B2 (ja) | 2002-09-30 | 2007-07-11 | 株式会社巴川製紙所 | 電子写真用トナーおよびそれを使用した画像形成方法 |
| JP4290442B2 (ja) * | 2003-02-28 | 2009-07-08 | 株式会社巴川製紙所 | 電子写真用トナー及びそれを用いた現像方法 |
| KR20050105505A (ko) * | 2003-02-28 | 2005-11-04 | 가부시키가이샤 도모에가와 세이시쇼 | 전자 사진용 현상제 |
| US7979006B2 (en) | 2005-02-28 | 2011-07-12 | Brother Kogyo Kabushiki Kaisha | Image forming apparatus and removable cartridge |
| JP4635645B2 (ja) * | 2005-02-28 | 2011-02-23 | ブラザー工業株式会社 | 画像形成装置及びトナーカートリッジ |
| JP4232747B2 (ja) * | 2005-02-28 | 2009-03-04 | ブラザー工業株式会社 | 画像形成装置 |
| JP4325572B2 (ja) * | 2005-02-28 | 2009-09-02 | ブラザー工業株式会社 | 画像形成装置 |
| JP5880410B2 (ja) * | 2012-11-29 | 2016-03-09 | 富士ゼロックス株式会社 | 静電荷像現像用透明トナー、静電荷像現像剤、トナーカートリッジ、現像剤カートリッジ、プロセスカートリッジ、画像形成装置及び画像形成方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0627714A (ja) * | 1992-04-01 | 1994-02-04 | Xerox Corp | カプセル化トナー組成物の製造法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1367581A (en) * | 1972-01-21 | 1974-09-18 | Int Synthetic Rubber | Polymer treatment process |
| JPS58149060A (ja) * | 1982-03-02 | 1983-09-05 | Nippon Zeon Co Ltd | 電子写真用トナ− |
| US5179171A (en) * | 1985-05-24 | 1993-01-12 | Mitsui Petrochemical Industries, Ltd. | Random copolymer, and process for production thereof |
| US5179156A (en) * | 1987-01-19 | 1993-01-12 | Sumitomo Chemical Company, Limited | Rubber composition |
| JP2520892B2 (ja) * | 1987-02-05 | 1996-07-31 | 三井石油化学工業株式会社 | トナ―用離型剤 |
| JPH087458B2 (ja) * | 1988-02-10 | 1996-01-29 | 富士ゼロックス株式会社 | 乾式トナー |
| US5039766A (en) * | 1988-06-28 | 1991-08-13 | Sumitomo Chemical Company, Limited | Liquid catalyst component, catalyst system containing said component and process for producing ethylene-alpha-olefin copolymer using said catalyst system |
| JPH02184864A (ja) * | 1989-01-12 | 1990-07-19 | Ricoh Co Ltd | 静電写真用現像剤 |
| JPH0754406B2 (ja) * | 1989-11-08 | 1995-06-07 | 株式会社巴川製紙所 | 静電荷像現像用トナー |
| JP2977595B2 (ja) * | 1989-11-20 | 1999-11-15 | 三井化学株式会社 | シンジオタクチックポリプロピレン成形体およびその製造方法 |
| JPH04358159A (ja) * | 1991-06-04 | 1992-12-11 | Toshiba Corp | 電子写真用現像剤 |
| IL107810A0 (en) * | 1992-12-17 | 1994-02-27 | Exxon Chemical Patents Inc | Functionalized polymers and processes for the preparation thereof |
| US5817843A (en) * | 1993-01-29 | 1998-10-06 | Nippon Shokubai Co., Ltd. | Quinizarin compound, method for production thereof, and use therefor |
| DE69509439T2 (de) * | 1994-06-02 | 1999-10-21 | Canon K.K., Tokio/Tokyo | Toner für die Entwicklung elektrostatischer Bilder |
| US5650254A (en) * | 1995-06-26 | 1997-07-22 | Fuji Xerox Co., Ltd, | Image formation process |
-
1995
- 1995-12-29 JP JP35406395A patent/JP3274052B2/ja not_active Expired - Fee Related
-
1996
- 1996-07-29 EP EP96925122A patent/EP0843223B1/en not_active Expired - Lifetime
- 1996-07-29 WO PCT/JP1996/002133 patent/WO1997005529A1/ja not_active Ceased
- 1996-07-29 KR KR10-1998-0700722A patent/KR100439513B1/ko not_active Expired - Fee Related
- 1996-07-29 DE DE69632732T patent/DE69632732T2/de not_active Expired - Lifetime
- 1996-07-29 ES ES96925122T patent/ES2222482T3/es not_active Expired - Lifetime
- 1996-07-29 US US09/000,330 patent/US7252918B2/en not_active Expired - Fee Related
- 1996-07-29 CN CN96196905A patent/CN1130603C/zh not_active Expired - Fee Related
- 1996-08-29 TW TW085110520A patent/TW509827B/zh not_active IP Right Cessation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0627714A (ja) * | 1992-04-01 | 1994-02-04 | Xerox Corp | カプセル化トナー組成物の製造法 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7049040B2 (en) * | 1996-12-26 | 2006-05-23 | Ticona Gmbh | Electrostatically charged image developing toner containing a polyolefin resin having a cyclic structure |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0843223A1 (en) | 1998-05-20 |
| CN1201533A (zh) | 1998-12-09 |
| EP0843223A4 (en) | 1998-10-28 |
| CN1130603C (zh) | 2003-12-10 |
| US7252918B2 (en) | 2007-08-07 |
| KR19990036057A (ko) | 1999-05-25 |
| TW509827B (en) | 2002-11-11 |
| JP3274052B2 (ja) | 2002-04-15 |
| ES2222482T3 (es) | 2005-02-01 |
| KR100439513B1 (ko) | 2004-10-08 |
| JPH09101631A (ja) | 1997-04-15 |
| US20020025485A1 (en) | 2002-02-28 |
| DE69632732D1 (de) | 2004-07-22 |
| DE69632732T2 (de) | 2005-06-30 |
| EP0843223B1 (en) | 2004-06-16 |
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