SU637099A3 - Electrographic developer - Google Patents

Electrographic developer

Info

Publication number
SU637099A3
SU637099A3 SU731953600A SU1953600A SU637099A3 SU 637099 A3 SU637099 A3 SU 637099A3 SU 731953600 A SU731953600 A SU 731953600A SU 1953600 A SU1953600 A SU 1953600A SU 637099 A3 SU637099 A3 SU 637099A3
Authority
SU
USSR - Soviet Union
Prior art keywords
modified
cycles
turn
quality
layering
Prior art date
Application number
SU731953600A
Other languages
Russian (ru)
Inventor
Е.Джонсон Гордон
Р.Линдблэнд Неро
Х.Шарп Джеймс
Original Assignee
Ксерокс Корпорейшн (Фирма)
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 Ксерокс Корпорейшн (Фирма) filed Critical Ксерокс Корпорейшн (Фирма)
Application granted granted Critical
Publication of SU637099A3 publication Critical patent/SU637099A3/en

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/097Plasticisers; Charge controlling agents
    • G03G9/09783Organo-metallic compounds
    • 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
    • G03G9/08742Binders for toner particles comprising macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds

Description

ку смешивают с носителем. После 15000 циклов, по сравнению с первым примером, качество копий остаетс  хорошим, а на фоторецепторе не наблюдаетс  вредного наслоени  виража.ku mixed with the carrier. After 15,000 cycles, compared to the first example, the copy quality remains good, and there is no harmful layering of the bend on the photoreceptor.

Пример 3. Про витель модифицирован таким же образом, что и в примере 2, добавлением 2,0% фталеврй кислоты, средн   величина частиц которой находитс  в пределах от 0,5-10 мк. После 5000 циклов качество копии, по сравнению с первым примером, лучше с меньшим наслоением виража на фоторецепторе.Example 3. The producer was modified in the same manner as in Example 2 by the addition of 2.0% phthalic acid, the average particle size of which is in the range of 0.5-10 microns. After 5000 cycles, the quality of the copy, as compared with the first example, is better with a smaller stratification of the turn on the photoreceptor.

Пример 4. Про витель модифициролан тем же способом, что во втором примере , добавлением 3,0% изофталевой кислоты , средний размер частиц которой колеблетс  от 0,5 до 10 мк. После 5000 циклов качество копий значительно лучше, чем в первом примере, при гораздо меньшем наслоении виража.Example 4. The producer is modified in the same manner as in the second example, by adding 3.0% isophthalic acid, the average particle size of which ranges from 0.5 to 10 microns. After 5000 cycles, the copy quality is much better than in the first example, with a much smaller layering of the turn.

Пример 5. Про витель модифицирован , как и в-примере 2, добавлением 1,0% соли натри  терефталевой кислоты, и полученной при взаимодействии 2 молей NaOH с 1 молем кислоты. Средние размеры частиц соли колеблютс  от 0,5-10 мк. После 7000 циклов качество копий значительно лучше, чем в первом примере.Example 5. The pro ductor is modified, as in Example 2, by adding 1.0% sodium salt of terephthalic acid, and obtained by reacting 2 moles of NaOH with 1 mole of acid. The average size of salt particles ranges from 0.5-10 microns. After 7000 cycles, the copy quality is significantly better than in the first example.

Пример 6. Про витель модифицирован как и в примере 2, добавлением 0,25% соли кали  изофталевой кислоты. Средний размер частиц соли колеблетс  в пределах от 0,5 до 10 мк. После 7000 циклов качество копий значительно лучше.Example 6. The manufacturer was modified as in example 2 by adding 0.25% potassium salt of isophthalic acid. The average salt particle size ranges from 0.5 to 10 microns. After 7000 cycles, the copy quality is much better.

Пример 7. Про витель модифицирован тем же способом, что в примере 2, добавлением 1,0% соли цинка терефталевой кислоты. Средний размер частиц соли - 0,5-10 мк. После 7000 циклов качество копий значительно лучше, чем в иримере 1.Example 7. The producer was modified in the same way as in Example 2 by adding 1.0% zinc salt of terephthalic acid. The average size of salt particles is 0.5-10 microns. After 7000 cycles, the copy quality is significantly better than in the irimer 1.

Пример 8. Про витель модифицирован тем же способом, что и в примере 2, добавлением соли аммони  терефталевой кислоты. Средний размер частиц соли 0,5- 10 мк. После 7000 циклов качество копий значительно лучше, чем в примере 1, при меньшем наслоении виража.Example 8. The producer was modified in the same manner as in Example 2 by the addition of an ammonium terephthalic acid salt. The average size of salt particles is 0.5-10 microns. After 7000 cycles, the quality of the copies is significantly better than in Example 1, with less turn layering.

Пример 9. Технологический ироыесс, описанный в примере I, но копировальноеExample 9. Technological and technological solutions described in example I, but copying

устройство оборздовано винилкарбазоловым фотопровод шим элементом. Уже после 500 копий, как и в примере 1, наблюдаетс  наслоение виража при заметном ухудшении качества копий.The device is surrounded by a vinylcarbazole photoconductor shim element. Already after 500 copies, as in Example 1, layering of the turn is observed with a noticeable deterioration in the quality of the copies.

Пример 10. Технологический процесс, оиисанный в примере 9, иовтор етс  за исключением того, что нагруженный виражем фотопровод ший элемент, даюший изображение того же состава, и про витель модифицирован добавлением терефталевой кислоты , средний размер частиц которой колеблетс  от 0,5 до Q.MK. Модификаци  образована простым однородным механическим перемешиванием терефталевой кислоты , вз той в количестве 0,29% от веса виража с виражом. После этого вираж и добавку смешивают с носителем. После После 15000 циклов качество копий остаетс  относительно однородным по сравнению с первым примером, а наслоение виража незначительно.Example 10. The technological process described in example 9 is repeated except that the photoconductor loaded with the turn is an image of the same composition and the developer is modified by adding terephthalic acid, the average particle size of which varies from 0.5 to Q. Mk. The modification is formed by simple homogeneous mechanical agitation of terephthalic acid, taken in an amount of 0.29% by weight of the turn with a turn. After that, the turn and the additive is mixed with the carrier. After 15,000 cycles, the quality of the copies remains relatively uniform compared to the first example, and the layering of the bends is negligible.

Опнсываемый электрографический модифицированный про витель обеспечивает длительное сохранение хорошего качества копий, а также минимальное наслоение виража на фотопровод шую поверхность элемента , даюшего зображение.The modified electrophotographic modified developer ensures long-term preservation of good quality of copies, as well as minimal layering of the bend on the photoconductive surface of the element giving the image.

Claims (1)

1. Патент США ЛЬ 3239465, кл. 252-62. I. 1966.1. US patent LI 3239465, cl. 252-62. I. 1966.
SU731953600A 1972-08-03 1973-08-02 Electrographic developer SU637099A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US277542A US3884825A (en) 1972-08-03 1972-08-03 Imaging composition

Publications (1)

Publication Number Publication Date
SU637099A3 true SU637099A3 (en) 1978-12-05

Family

ID=23061309

Family Applications (1)

Application Number Title Priority Date Filing Date
SU731953600A SU637099A3 (en) 1972-08-03 1973-08-02 Electrographic developer

Country Status (11)

Country Link
US (1) US3884825A (en)
JP (1) JPS5410254B2 (en)
BE (1) BE802878A (en)
BR (1) BR7305960D0 (en)
CA (1) CA1009492A (en)
DE (1) DE2326273A1 (en)
FR (1) FR2194992B1 (en)
GB (1) GB1437042A (en)
IT (1) IT991465B (en)
NL (1) NL7310672A (en)
SU (1) SU637099A3 (en)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52113739A (en) * 1976-03-19 1977-09-24 Canon Inc Electrostatically developing toner
JPS52136635A (en) * 1976-05-12 1977-11-15 Toshiba Corp Electrostatic image developing toner
JPS587284Y2 (en) * 1978-04-08 1983-02-08 宇部興産株式会社 angle measuring instrument
US4410617A (en) * 1982-04-12 1983-10-18 Xerox Corporation Colored toner and developer composition
US4411974A (en) * 1982-04-12 1983-10-25 Xerox Corporation Ortho-halo phenyl carboxylic acid charge enhancing additives
US4411975A (en) * 1982-04-12 1983-10-25 Xerox Corporation Para-halo phenyl carboxylic acid charge enhancing additives
US4442189A (en) * 1983-01-26 1984-04-10 Xerox Corporation Toner compositions containing polyanhydride resins
US5162557A (en) * 1988-07-27 1992-11-10 Synthetic Products Company Ruthenium aromatic polycarboxylates
US4963127A (en) * 1988-07-27 1990-10-16 Synthetic Products Company Stannic terephthalate
US5026888A (en) * 1988-07-27 1991-06-25 Synthetic Products Company Ruthenium terephthalate
US5164458A (en) * 1989-04-28 1992-11-17 Synthetic Products Company High performance engineering polymer compositions
US4983688A (en) * 1989-04-28 1991-01-08 Synthetic Products Company Liquid crystal polymer compositions
US5296585A (en) * 1989-04-28 1994-03-22 Synthetic Products Company Polymeric metal terephthalate and isophthalate fibers and method of making
US5176977A (en) * 1991-07-01 1993-01-05 Eastman Kodak Company Nonpolymeric amorphous developer compositions and developing processes
US5358814A (en) * 1993-08-31 1994-10-25 Eastman Kodak Company Toner compositions containing as a negative charge-controlling agent a mixture of ortho-benzoic sulfimide and para-anisic acid
US5358815A (en) * 1993-08-31 1994-10-25 Eastman Kodak Company Toner compositions containing negative charge-controlling additive
US5358817A (en) * 1993-08-31 1994-10-25 Eastman Kodak Company Toner compositions containing as a negative charge-controlling agent the calcium salt of ortho-benzoic sulfimide
US5358818A (en) * 1993-08-31 1994-10-25 Eastman Kodak Company Ortho-benzoic sulfimide as charge-controlling agent
US5358816A (en) * 1993-08-31 1994-10-25 Eastman Kodak Company Zinc salt of ortho-benzoic sulfimide as negative charge-controlling additive for toner and developer compositions
US5332637A (en) * 1993-08-31 1994-07-26 Eastman Kodak Company Electrostatographic dry toner and developer compositions with hydroxyphthalimide

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2940934A (en) * 1953-06-22 1960-06-14 Haloid Xerox Inc Electrostatic developer composition and method therefor
US2893976A (en) * 1957-03-28 1959-07-07 Monsanto Chemicals Color stable blends of styrene polymers and rubbery diene polymers containing azo dyes and terephthalic or isophthalic acid
BE594397A (en) * 1959-09-04
NL286305A (en) * 1961-12-16
US3510338A (en) * 1965-08-06 1970-05-05 Inmont Corp Method of electrostatic printing
US3590000A (en) * 1967-06-05 1971-06-29 Xerox Corp Solid developer for latent electrostatic images
NL7213836A (en) * 1971-10-12 1973-04-16 Electrophotographic dry toner developer - contg fatty acid salt and hydrophobic colloidal silica
ZA763694B (en) * 1975-06-24 1977-08-31 Kenlowe Accessories & Co Ltd An ignition system

Also Published As

Publication number Publication date
GB1437042A (en) 1976-05-26
JPS4960229A (en) 1974-06-11
IT991465B (en) 1975-07-30
FR2194992A1 (en) 1974-03-01
NL7310672A (en) 1974-01-25
DE2326273A1 (en) 1974-02-14
BR7305960D0 (en) 1974-07-25
BE802878A (en) 1973-11-16
FR2194992B1 (en) 1977-05-13
CA1009492A (en) 1977-05-03
US3884825A (en) 1975-05-20
JPS5410254B2 (en) 1979-05-02
AU5890873A (en) 1975-02-06

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