DE2111985A1 - Electrostatographic, liquid developer - Google Patents
Electrostatographic, liquid developerInfo
- Publication number
- DE2111985A1 DE2111985A1 DE19712111985 DE2111985A DE2111985A1 DE 2111985 A1 DE2111985 A1 DE 2111985A1 DE 19712111985 DE19712111985 DE 19712111985 DE 2111985 A DE2111985 A DE 2111985A DE 2111985 A1 DE2111985 A1 DE 2111985A1
- Authority
- DE
- Germany
- Prior art keywords
- developer
- electrostatographic
- dispersion
- carrier liquid
- liquid
- 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.)
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- 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
- G03G9/12—Developers with toner particles in liquid developer mixtures
- G03G9/135—Developers with toner particles in liquid developer mixtures characterised by stabiliser or charge-controlling agents
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/122—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
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- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10M2207/283—Esters of polyhydroxy compounds
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- C10M2207/286—Esters of polymerised unsaturated acids
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
- C10M2219/066—Thiocarbamic type compounds
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
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- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
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- C10M2223/041—Triaryl phosphates
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- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
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Description
Bank Xerox Limited, Rank Xerox House, 338 iuston Road M Iiondon, K.W»19 EnglandBank Xerox Limited, Rank Xerox House, 338 iuston Road M Iiondon, KW »1 9 England
Elektrostatographischer, flüssiger EntwicklerElectrostatographic liquid developer
Die Erfindung betrifft einen elektroatatographiachen, flüssigen Entwickler vw.ä ein Verfahren» xm ein elektroatatisches latentes Bild zu entwickeln*The invention relates to an electroatatographic, liquid developer vw.ä a method » xm to develop an electroatatic latent image *
Blektrodtatographisohe,flüssige Entwickler enthalten im allgemeinen ein elektrisches Isolierdispersionsmedium (eine ülr'ägerflüssigkeit) und einen feinverteilten Toner (i« allgemeinen in Submikronteilchen), der in der Trägerflüssiglcelt dispergiert ist und ein Hgment und ein harzförmigee Material enthält.Blektrodtatographisohe, liquid developers are contained in the generally an electrical insulating dispersion medium (a carrier liquid) and a finely divided toner (generally in submicron particles) that is present in the carrier liquid is dispersed and a hgment and a resinous one Contains material.
Jm allgemeinen muß die !Erägerflüssigkeit einen elektrischenIn general, the liquid must be electric
gptgifisehen Widerstand von nicht weniger als 10 Ohm-cm /bteitses! und geeignete !Erägerflüssigkeiten schließen Cyclo- htxan, i^cahydronaphthalin (beispielsweise Decalin), iso-Kohlenwasserstoff», ohlorfluorierte Kohlenoffe, Kerosin und verschiedene Qualitäten von handelsüblichem öaaolin bzw. Benzin ein.Optimal resistance of not less than 10 ohm-cm / bteites! and suitable carrier fluids include cyclohexane , hydronaphthalene (e.g., decalin), isohydrocarbons, chlorofluorocarbons, kerosene, and various grades of commercially available petrol.
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Pigmente, die für den Toner geeignet sind, schließen ein. Ruß und Phthalocyaninpigmente. Alkydharze und verschiedene Lacke können als Mittel zur Regulierung der ladung verwendet werden.Pigments suitable for the toner include. Carbon black and phthalocyanine pigments. Alkyd resins and various varnishes can be used as a means of regulating the charge will.
Viele Verfahren sind bekannt, um die Tonerteilchen in der ' Trägerflüssigkeit zu dispergieren. Bevor man die Pigmentteilchen in der Trägerflüssigkeit dispergiert, müssen sie erst in feinverteilter Form in dem harzförmigen Material dispergiert sein· Pur diesen Zweck verwendet man verschiedene Vorrichtungen wie Kugelmühlen, Mühlen mit drei Walzen oder Sandmühlen. Dadurch erhält man eine homogene Mischung, die harzförmiges Material und das Pigment enthält und die manchmal als Paste oder.als Konzentrat bezeichnet wird. Eine solche Paste kann anschließend mit der Trägerflüssigkeit verdünnt oder in einem großen Volumen der Trägerflüssigkeit unter Bildung des flüssigen Entwicklers dispergiert werden« Um die Di3persion3Etabilität des verdünnten Entwicklers au erhöhen, kann man andere Zusatzstoffe wie oberflächenaktive Mittel einarbeiten.Many methods are known to disperse the toner particles in the carrier liquid. Before dispersing the pigment particles in the carrier liquid, they must first in finely divided form in the resinous material be dispersed · Pur this purpose using different devices such as ball mills, mills with three rolls or sand mills. This results in a homogeneous mixture that contains the resinous material and the pigment and which is sometimes referred to as a paste or concentrate. Such a paste can then be diluted with the carrier liquid or dispersed in a large volume of the carrier liquid to form the liquid developer. In order to increase the dispersion stability of the diluted developer, other additives such as surface-active agents can be incorporated.
Man erhält so durch recht einfache Verfahren flüssige Entwickler, die eine zufriedenstellende Dispersionsstabilität aufweisen.Liquid developers which have a satisfactory dispersion stability are obtained in this way by quite simple processes exhibit.
Zusätzlich su den oben beschriebenen Verfahren kann konzentrierte Dispersionen wie Druckfarben. Teer oder Pech verwenden, in denen Pigmentteilchen bereits in harzförmigen Trägerstoffen dispergiert sind. Die stabilen, verdünnten Dispersionen können dann hergeeteilt werdsn, indem man einfach die konzentrierte Dispersion in Träger- flüssigkeiten löst, beispielsweise unter Verwendung einer Ultraschallvorrichtung. In addition to the methods described above, concentrated dispersions such as printing inks can be used. Use tar or pitch in which pigment particles are already dispersed in resinous carriers. The stable, dilute dispersions can then be divided up by simply dissolving the concentrated dispersion in carrier liquids, for example using an ultrasonic device.
Ein elektrophotographischer, flüssiger Entwickler muß jedoch andere wichtige Erfordernisse zusätzlich zu der However, an electrophotographic liquid developer has other important requirements in addition to
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Dispersionsstabilität erfüllen, d.h. er sollte eine hohe Widerstandsfähigkeit "besitzen, und die Tonerteilchen sollten eine "bestimmte Ladungspolarität aufweisen, entweder negativ oder positiv.Satisfy dispersion stability, that is, it should have high resistance ", and the toner particles should "have a certain charge polarity, either negative or positive.
Es ist im allgemeinen schwierig, die letztere Eigenschaft, die Ladungspolarität, zu regulieren und die Anzahl der harzförinigen Materialien, die geeignet sind, um die Ladung zu regulieren, ist recht begrenzt. Üblicherweise werden Alkydharze und Leinsamenöl nicht nur als Träger für Pigmente, sondern ebenfalls als geeignete Ladungsreguliermittel verwendet, um den dispergierten Teilchen eine positive Ladung zu verleihen. Versuche haben jedoch gezeigt, daß die Verwendung von Alkydharz oder Leinsamenöl für den vorliegenden Zv/eck, besonders wenn man Druckerschwärzen, Teer oder Pech verwendet, recht zweifelhaft ist.It is generally difficult to regulate the latter property, charge polarity, and the number of resinous materials that are suitable to regulate the charge is quite limited. Usually Alkyd resins and linseed oil are not only used as carriers for pigments, but also as suitable charge control agents used to impart a positive charge to the dispersed particles. Attempts have however showed that the use of alkyd resin or linseed oil for the present case, especially when printing inks, Tar or pitch used is quite doubtful.
Um die elektrophoretisch^ Wirkung eines Entwicklers zu verbessern, werden oft bestimmte Zusatzstoffe verendet» Es ist wünschenswert, daß sie in der Trägerflüssigkeit löslich sind und daß sie die Eigenschaft besitzen, die Ladung gut zu regulieren, ohne daß der spezifische Widerstand des betreffenden Entwicklers zu stark vermindert wird. Es ist nur eine sehr beschränkte Anzahl von Verbindüngen, die diese Erfordernisse erfüllen, bekannt. Ein typisches Beispiel sind bestimmte metallorganische Verbindungen. To improve the electrophoretic ^ effect of a developer, Certain additives are often used »It is desirable that they be soluble in the carrier liquid and that they have the property of regulating the charge well without affecting the specific resistance of the developer concerned is reduced too much. It is only a very limited number of connections which meet these requirements are known. A typical example are certain organometallic compounds.
Gegenstand der Erfindung ist ein elektrostatographiseher, flüssiger Entwickler, der eine elektrische Isolierträgerflüssigkeit und einen feinverteilten Toner, dispergiert in der Trägerflüssigkeit, und ein harzförmiges Material enthält. Der erfindungsgemäße elektrostatographische, flüssige Entwickler ist dadurch gekennzeichnet, daß er mindestens eine Verbindung, ausgewählt unter Vinyltri-The subject of the invention is an electrostatographic, liquid developer that disperses an electrically insulating carrier liquid and a finely divided toner in the carrier liquid, and a resinous material. The inventive electrostatographic, liquid developer is characterized in that it contains at least one compound selected from vinyl tri-
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äthoxysilan, ^-Glycidoxypropyltrimethoxysilan und ß-(3,^EpoxycyclohexylJ-äthyltrimethoxysilan, enthält.äthoxysilan, ^ -Glycidoxypropyltrimethoxysilan and ß- (3, ^ EpoxycyclohexylJ-äthyltrimethoxysilan contains.
Gagenstand der vorliegenden Erfindung ist ebenfalls ein Verfahren, um ein elektrostatisches latentes Bild zu entwickeln, das darin besteht, daß man -das elektrostatische latente Bild mit dem erfindungsgemäßen Entwickler behandelt. Fee status of the present invention is also a A method of developing an electrostatic latent image which consists of having the electrostatic latent image treated with the developer according to the invention.
Für die meisten Anwendungen ist es wünschenswert, daß der Toner einen farbgebenden Bestandteil enthält (der Ausdruck "Farbe," schließt die Farben schwarz und weiß ein), beispielsweise einen Farbstoff und/oder ein Pigment.For most applications it is desirable that the toner contain a coloring component (the term "Color," includes the colors black and white), for example a dye and / or a pigment.
Verwendet man eine oder mehrere der oben angegebenen drei siliciumorganischen Verbindungen, so ist es möglich, unter geeigneter Kontrolle der Bestandteile und der Anteile einen elektrostatographischen, flüssigen Entwickler herzustellen, der ausreichend hohe elektrische Widerstandsfähigkeit besitzt und nur positiv geladene Tonerteilchen enthält.Using one or more of the three organosilicon compounds mentioned above, it is possible to manufacture an electrostatographic liquid developer, under appropriate control of the ingredients and proportions, the sufficiently high electric resistance has and contains only positively charged toner particles.
Allgemein gesagt gilt, daß siliciumorganische Verbindungen ausreichend polar sind, um sich in Alkohol, Aceton und in einigen Fällen in Wasser zu lösen. Es wurde festgestellt, daß Verbindungen, die in Wasser löslich sind, die spezifische Widerstandsfähigkeit des Entwicklers zu stark erniedrigen und für den vorliegenden Zweck daher nicht geeignet sind.Generally speaking, organosilicon compounds are sufficiently polar to dissolve in alcohol, acetone, and in some cases, water. It was determined, that compounds which are soluble in water increase the specific resistance of the developer and are therefore not suitable for the present purpose.
Überraschenderweise sind die drei obengenannten Verbindungen geeignet,als Mittel» um die Ladung in elektrostatographischen Entwicklern zu regulieren, Verwendung zu finden, da sie in vielen nicht-polaren Lösungsmitteln wie Cyclöhexan, Kerosin, Decahydronaphthalin, Toluol, Xylol und isoparaffinisehen Kohlenwasserstoffen löslich sind.Surprisingly, the three above-mentioned compounds are suitable as a means of increasing the charge in electrostatographic Developers regulate their use, as they can be found in many non-polar solvents such as Cyclohexane, kerosene, decahydronaphthalene, toluene, xylene and isoparaffinic hydrocarbons are soluble.
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Die bemerkenswerte Bedeutung der vorliegenden Erfindung liegt in der Tatsache, daß sie Entwickler, die ganz ausgezeichnet wirken, zur Verfugung stellt und daß es nicht erforderlich ist, komplizierte technische Verfahren anzuwenden, sondern man gibt einfach die oben erwähnten Verbindungen in die Dispersion. Da die erfindungsgemäßen Entwickler nur positiv geladene Toner einschließen, kann man ein entwickeltes Bild mit verbesserter optischer Dichte erhalten, wenn man den erfindungsgemäßen Entwickler verwendet.The remarkable importance of the present invention lies in the fact that they are developers who are quite excellent act, provides and that it is not required is to use complicated technical processes, but simply add the above-mentioned compounds to the dispersion. Since the developers of the present invention include only positively charged toners, one can use a developed one Image with improved optical density obtained using the developer of the present invention.
Durch die vorliegende Erfindung wird es möglich, eine große Vielzahl von harzförmigen Materialien zu verwenden. Harzförmiges Material, das Entwickler liefert, die nicht annehmbar sind, wenn es a,llein verwendet wird, ergibt gute Entwickler zusammen mit den angegebenen siliciumorganischen Verbindungen. Der Fortschritt ist in Bezug auf die elektrophoretischen Wirkungen ausgeprägter als in Bezug auf die Dispersionsstabilität.The present invention enables a wide variety of resinous materials to be used. Resin-shaped Material that provides developers that are unacceptable when used alone make good ones Developer together with the specified organosilicon compounds. The progress is in terms of that electrophoretic effects more pronounced than in relation to the dispersion stability.
Die oben erwähnten Verbindungen können ebenfalls verwendet werden, um die elektrophoretischen Wirkungen von Dispersionen zu verbessern, die aus im Handel erhältlichen Druckerschwärzen, Teer oder Pech hergestellt wurden, um Entwickler mit positiver Polarität zu bilden.The above mentioned compounds can also be used to increase the electrophoretic effects of dispersions made from commercially available printing ink, tar, or pitch to make developers with positive polarity to form.
Wie oben erwähnt, wird durch die vorliegende Erfindung die Anzah^ an Rohmaterialien, die bei elektrostatographischen Entwicklern verwendet werden können, stark vergrößert, und in einigen Pällen wird durch die vorliegende Erfindung die Herstellung des flüssigen Entwicklers, der einen positiv geladenen Toner enthält, vereinfacht.As mentioned above, the present invention increases the number of raw materials used in electrostatographic Developers can be used, greatly enlarged, and in some cases is supported by the present invention simplifies the manufacture of the liquid developer containing a positively charged toner.
Um die Konzentration der siliciumorganischen Verbindungen in dem Entwickler zu bestimmen, muß man die spezifische Widerstandsfähigkeit des entstehenden Entwicklers beachten.About the concentration of the organosilicon compounds To determine in the developer, one must consider the resistivity of the developing developer.
109839/1*12109839/1 * 12
·■ O ·*■· ■ O · * ■
Arbeitet man eine zu geringe Menge ein, so ist die ladungsreguiierende Wirkung nicht ausreichend. Die praktische untere Grenze der Konzentration beträgt ungefähr 0,5 Vol.-$. Die obere Grenze der Konzentration beträgt ungefähr 2 Vol.-#. Über dieser Grenze wird die Widerstandsfähigkeit des Entwicklers im allgemeinen auf solche Weise ernie-. drigt, daß sich ein elektrostatisches latentes Bild schnell bei einem Kontakt mit dem Entwickler entlädt, und in einigen Fällen tritt Koagulation des Toneis auf.If too small an amount is worked in, the charge-regulating amount is Effect not sufficient. The practical lower limit of the concentration is about 0.5 volume percent. The upper limit of the concentration is approximately 2 vol. #. Resistance will be above this limit of the developer in general in such a way. drigt that there is an electrostatic latent image rapidly discharges upon contact with the developer, and in some cases coagulation of the clay occurs.
Die folgenden Beispiele erläutern die Erfindung ohne sie jedoch zu beschränken.The following examples illustrate the invention without it however to restrict.
5 g schwarze Offset-Druckerschwärze "Jet King G process H Black" von der !oyo Ink Manufacturing Co. wurden in 1000 ml Kerosin durch eine Ultraschalldispersionsvorrichfcung dispergiert, Zu der entstehenden Dispersion fügte man 10 g Vinyltriäthoxysilan CH2=CHSi(OC2Hc)3, das bei der Shin-etsu Chemical Ind. unter dem Handelsnamen "KBE IOO3+11 gekauft wurde. Die dispergiarten Rußteilchen wurden positiv geladen und zeigten als elektrostatographischer, · flüssiger Entwickler eine gute Wirkung. Verwendete man diese Dispersion für ein elektrostatographisches latentes Bild, das man hergestellt hatte» indem man eine photoleitfähige Überzugsschicht, die auf einem geerdeten, leitfähigen Substrat lag, auflud und den geladenen Überzug mit einem Bild aus Licht und Schatten belichtete, so erhielt man ein schwarzes Tonerbild, das eine zufriedenstellende optische Dichte zeigte.5 g of black "Jet King G process H Black" offset printing ink from! Oyo Ink Manufacturing Co. were dispersed in 1000 ml of kerosene using an ultrasonic dispersion device. 10 g of vinyltriethoxysilane CH 2 = CHSi (OC 2 Hc) were added to the resulting dispersion. 3 , which was purchased from Shin-etsu Chemical Ind. Under the trade name "KBE 1003 + 11. The dispersible carbon black particles were positively charged and worked well as an electrostatographic liquid developer. When this dispersion was used for an electrostatographic latent image, the prepared "by charging a photoconductive coating layer overlying a grounded conductive substrate and exposing the charged coating to an image of light and shadow, a black toner image exhibiting satisfactory optical density was obtained.
Eine ähnliche Dispersion ohne Vinyltriäthaxysilan enthielt \ ebenfalls positiv geladene lonerteilchen, aber die elektrophoretische 'Wirkung unterschied sich von Ansatz zu Ansatz der ursprünglichen Druckfarbe. Zugabe dor Silanverbiudung verhinderte ein solches Ändern der Eigenschaften.A similar dispersion without Vinyltriäthaxysilan also containing positively charged lonerteilchen, but the electrophoretic 'effect different from batch to batch of the original ink \. Addition of the silane compound prevented such a change in properties.
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2 g Channel-Ruß und 50 g Alkydharz, das von der Japan Reichhold Chemical Ind. unter dem Handelsnamen "Beckosol EL· 8002" gekauft war, wurden in einer 500 ml Kugelmühle ungefähr 2 Tage vermischt. Me so hergestellte konzentrierte Paste wurde in 2000 ml isoparaffinischem Lösungsmittel (Isopar H von der Esso Petroleum erhältlich) di~ spergiert. In dieser Dispersion nahm der Hauptteil der Tonerteilchen eine positive Ladung an, aber Teilchen mit negativer Polarität waren ebenfalls vorhanden. Dies ergab ein Tonerbild niedriger Dichte, wenn man die Dispersion zur Entwicklung eines elektrostatischen latenten Bilds mit negativer Polarität verwendete, wobei Haloes bzw. Ringe.und Streifen in den Bildbereichen mit hohem Kontrast auftraten.2 g of Channel carbon black and 50 g of alkyd resin from Japan Reichhold Chemical Ind. Under the trade name "Beckosol EL * 8002 "was purchased in a 500 ml ball mill mixed for about 2 days. The concentrated paste thus prepared was dissolved in 2000 ml of isoparaffinic solvent (Isopar H available from Esso Petroleum) disperses. In this dispersion took the main part of the Toner particles showed a positive charge, but particles with negative polarity were also present. This revealed a low density toner image when using the dispersion to develop an electrostatic latent Image with negative polarity, with haloes or rings and stripes in the image areas with high Contrast occurred.
Einarbeitung von 1 Vol.-$ ß-(3»4-Epoxycyclohexyl)-athyltrimethoxysilan ("KBM3O3" von Shin-etsu Chemical Ind.) in die obige Dispersion eliminierte Teilchen mit negativer Polarität. Wurde diese Dispersion zur Entwicklung eines negativen elektrostatischen latenten Bilds verwendet, so wurde die Anzahl von Haloes und Streifen vermindert "und die Bilddichte wurde erhöht.Incorporation of 1 vol .- $ ß- (3 »4-epoxycyclohexyl) -ethyltrimethoxysilane ("KBM3O3" by Shin-etsu Chemical Ind.) In the above dispersion eliminated particles with negative Polarity. When this dispersion was used to develop a negative electrostatic latent image, so the number of haloes and stripes was decreased "and the image density was increased.
ß-(3»4-Epoxycyclohexyl)-athyltrimethoxysilan.β- (3 »4-epoxycyclohexyl) -ethyltrimethoxysilane.
Eine homogene Paste wurde hergestellt, indem man 200 g S-4-Xaok von der Toyo Ink Manufacturing Co. und 10 g Channel-Ruß auf einer Drei-Walzen-Mühle vermischte. 50 g dieser Paste wurden in 2000 ml Kerosin in einer Ultraschall-A homogeneous paste was prepared by adding 200 g of S-4-Xaok made by Toyo Ink Manufacturing Co. and 10 g Channel carbon black blended on a three-roll mill. 50 g of this paste were in 2000 ml of kerosene in an ultrasonic
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dispersionsvorriehtung dispergiert. Die elektrophoretischen Eigenschaften dieser Dispersion waren stark variierbar, abhängig von den Herstellungsbedingungen, und bei dem obigen Beispiel erhielt man ein sehr unklares Bild mit niedriger Dichte, wenn man die Dispersion zur Entwicklung eines elektrostatischen latenten Bilds mit negativer Polarität verwendete. Wurden 1,5 Vol.-# ^"-Grlycidoxypropyltrimethoxysilan ("KBM 403" von der Shin-etsu Chemical Ind.) zu der Dispersion zugefügt, so verschwand die WirkungsSchwankung, und der Toner hatte eine stabile positive Ladung.Dispersionsvorriehtung dispersed. The electrophoretic properties of this dispersion varied widely depending on the manufacturing conditions, and in the above example, a very unclear, low density image was obtained when the dispersion was used to develop an electrostatic latent image of negative polarity. When 1.5 vol. # ^ "-Grlycidoxypropyltrimethoxysilane (" KBM 403 "from Shin-etsu Chemical Ind.) Was added to the dispersion, the fluctuation in effect disappeared and the toner had a stable positive charge.
CH2 —CHCH2(CH2)5Si(OCH3)CH 2 —CHCH 2 (CH 2 ) 5 Si (OCH 3 )
^-Glycidoxypropyltrimethoxysilan,^ -Glycidoxypropyltrimethoxysilane,
109839/1612109839/1612
Claims (2)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP45020984A JPS4843157B1 (en) | 1970-03-12 | 1970-03-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2111985A1 true DE2111985A1 (en) | 1971-09-23 |
Family
ID=12042402
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19712111985 Pending DE2111985A1 (en) | 1970-03-12 | 1971-03-12 | Electrostatographic, liquid developer |
Country Status (6)
Country | Link |
---|---|
US (1) | US3729419A (en) |
JP (1) | JPS4843157B1 (en) |
CA (1) | CA963305A (en) |
DE (1) | DE2111985A1 (en) |
FR (1) | FR2084788A5 (en) |
GB (1) | GB1341627A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5208130A (en) * | 1989-07-31 | 1993-05-04 | Spectrum Sciences B.V. | Charge director compositions for liquid developer |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3841893A (en) * | 1970-03-12 | 1974-10-15 | Rank Xerox Ltd | Charge control agents for liquid developers |
US3976808A (en) * | 1973-05-29 | 1976-08-24 | Xerox Corporation | Imaging systems |
US3926825A (en) * | 1973-05-29 | 1975-12-16 | Xerox Corp | Liquid developer composition and process for preparing same |
US4019911A (en) * | 1973-11-19 | 1977-04-26 | Pitney-Bowes, Inc. | Toner compositions |
US3939087A (en) * | 1973-11-19 | 1976-02-17 | Pitney-Bowes, Inc. | Toner compositions containing silane treated fumed silica |
US4059444A (en) * | 1974-03-14 | 1977-11-22 | Xerox Corporation | Liquid development using conductive inks |
US5570173A (en) | 1994-10-31 | 1996-10-29 | Xerox Corporation | Color printer using liquid developer |
US6289191B1 (en) | 1999-11-26 | 2001-09-11 | Xerox Corporation | Single pass, multicolor contact electrostatic printing system |
US6122471A (en) * | 1999-12-08 | 2000-09-19 | Xerox Corporation | Method and apparatus for delivery of high solids content toner cake in a contact electrostatic printing system |
US6256468B1 (en) | 2000-03-13 | 2001-07-03 | Xerox Corporation | Toner cake delivery system having a carrier fluid separation surface |
US6219501B1 (en) | 2000-03-28 | 2001-04-17 | Xerox Corporation | Method and apparatus for toner cake delivery |
US6311035B1 (en) | 2000-06-16 | 2001-10-30 | Xerox Corporation | Reprographic system operable for direct transfer of a developed image from an imaging member to a copy substrate |
US6526244B1 (en) | 2001-11-21 | 2003-02-25 | Xerox Corporation | Hybrid electrophotographic apparatus for custom color printing |
US6682865B2 (en) | 2001-11-21 | 2004-01-27 | Xerox Corporation | Hybrid electrophotographic apparatus for custom color printing |
-
1970
- 1970-03-12 JP JP45020984A patent/JPS4843157B1/ja active Pending
-
1971
- 1971-03-05 US US00121537A patent/US3729419A/en not_active Expired - Lifetime
- 1971-03-11 CA CA107,472A patent/CA963305A/en not_active Expired
- 1971-03-12 DE DE19712111985 patent/DE2111985A1/en active Pending
- 1971-03-12 FR FR7109434A patent/FR2084788A5/fr not_active Expired
- 1971-04-19 GB GB2373371*A patent/GB1341627A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5208130A (en) * | 1989-07-31 | 1993-05-04 | Spectrum Sciences B.V. | Charge director compositions for liquid developer |
Also Published As
Publication number | Publication date |
---|---|
US3729419A (en) | 1973-04-24 |
FR2084788A5 (en) | 1971-12-17 |
CA963305A (en) | 1975-02-25 |
JPS4843157B1 (en) | 1973-12-17 |
GB1341627A (en) | 1973-12-25 |
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