CA1158090A - One part magnetic toner powder including a fluoroaliphatic surface treatment composition - Google Patents

Abstract

201,417 CAN/JVL

ABSTRACT

A one-part, flowable, dry, electrostatically attractable toner powder comprising (a) particles each comprising a blend of from about 30 to 80 parts by weight thermoplastic binder and, correspondingly, from about 70 to 20 parts by weight magnetically responsive material; and (b) a surface treatment composition comprising 0.1 to 2 parts by weight fluoroaliphatic compound per 100 parts by weight of said particles. The toner powder possesses humidity resistance and improved image quality, particularly in terms of image sharpness.

Description

I1~8~9(~ 201,417 CAN/JVL

Description ONE-PART TONER POWDER COMPOSITION

Technical Field This invention relates to dry powder composi-tions suitable for use in elec~royraphic recording. Moreparticularly, it relates to heat-fusible and pressure-fixable one part toner powders that have a surface treat-ment comprisin~ a fluoroaliphatic compound attached to the surface of the individual toner powder particles.

_ackground Art One-part toner powder formulations ~sometimes known as single- or mono-component toners) are known.
They differ Erom two-part or two component developing powders in that they do no~ utilize a mixture oE carrier particles and toner powder particles to make up the developing powder composition. Rather, one-part toner powders are magnetically responsive and do not utilize a carrier to develop the electrostatic image.
One-part toner powders may he either heat-~usible or pressure-Eixable. ~eat-fusible toner powders are typically fixed after image formation by raising the temperature of the powders to their melting or softening point causing the powder particles to coalesce, flow together and adhere to the substrate. Pressure-fixable toner powders are typically fixed after image for~ation by simply applying pressure to the powder particles causing them to coalesce and adhere to the substrate.
Although both heat-fusible and pressure-ixable toner powders have been widely used and have enjoyed com-30 mercial succe~s, they often suffer from certain disadvan-tages. For example, the images produced wi~h such powders generally have poor resolution. Thus, they lack sharp edge definition and openings in the images, such as in the letters A, a, B, b, D, d, and O, suffer ~rom "fu~zy-fill~

. ., , ' .

~ 1~80g()

-2-ln" ~i.e., ther~ is slgnificant toner deposited in such openings ~herebv rendering the~ indistinct). Addition-ally, there is a substantial deposition oE toner ln non-image areas, i.e., ~ackground, particularly ~ne areas 5 between letters. Consequently, tne resultant photocopies are messy in appearance and frequently are difficult to read.
Additionally, the flow properties and developing characteristics of such one-part toner powders are o~ten 10 adversely affected by conditions of high humidity. Thus, they may resist flow, e.g., by caking or forming clumps, resulting in streaking on the finis~led copy. Such caking or clumping may also cause clogging in the development station leading to poor development and transfer of the toner powder and, consequently, poor copy quality.
The foregoing disadvantages are overcome in the present invention by surface treating the toner powder particles with a composition comprising a fluoroaliphatic compound.
Although the use of fluorochemical materials has been disclosed previously, see U.S. Patents 3,798,167, 4~002r570j 4,073,~80; 4,139,483, 4,198,477; British Patent 2,034,907; and copending U.S. application serial number 84,607 filed October 15, 1979 and now U.S. Patent ~5 4,268,598, applicant is aware of no disclosure of the use of a treatment composition comprising a fluoroaliphatic compound as a surface treatment for a one-part toner powder.
Of the above-mentioned patents, all except the British Patent and the copending United States application disclose the use of fluorochemical materials with two component developing powder compositions. For example, U.S. Patent 3,798,167 discloses the application of a coating of a fluoropolymer, or optionally, a mixture of a fluoropolymer and a modifying resin, to a carrier material. U.S. Patent 4,002,570 discloses a three component developer composition that comprises carrier 1 15809() particles, toner par~icles) ~nd a lubricant comprising a particulate, cross-linked polyvinylidene fluoride. The polyvinylidene fluoride particles are said to lubricate and act as effective photoreceptor cleaning materials. United States Patent 4,073,980 discloses a two component developing composition wherein the carrier particles have a mixture of a perfluoroacid and molybdenum disulfide coated on their surface. United States Patents 4,139,483, and 4,198,477 dis-close tt~o-part developer compositions wherein a fluorinated surface active additive is dispersed throughout, rather than coated on, the binder of the toner portion of the composition.
~luorochemical materials have also been previously utilized with one-part toner powders. Thus, British Patent 2,034,907 A ~published June 11, 1980) discloses a toner powder having a magnetic material distributed throughout a binder resin. A low molecular weight fluorine-containing surface active agent is applied to the surface of the magnetic material before the magnetic material is distributed throughout the binder.
Copending United States applica~ion 84,607, filed October 15, 1979, now United States Patent 4,268,598, describes a mixture of a sulfona-mido surface active material and a toner powder. The resultant mixture has two discrete components, i.e., the surface active material and the toner powder.

~0 Summary of the Invention In accordance with one aspect of the present invention, there is provided a one-part, flowable, dry, electrostatically attractable toner powder comprising (a) particles each comprising a blend of from about 30 to 80 parts by weight thermoplastic binder and, correspondingl~ from about 70 to 20 parts b~ weight magnetically responsive material; and 09(1 ~ b) a layer of a surface treatment composition attached to each of said particles at or near the ou~er surface of said par~icles, said surface treatment composition comprising from about 0.1 to 2 parts by weight fluoro-aliphatic compound per 100 parts by weight of said particles.
According to another aspect of the present invention there is provided a method of electrographic recording comprising: forming a differen-tial image pattern of a one-part, flowable, dry, electrostatically attractable toner powder comprising ~a) particles each comprising a blend of from about 30 to 80 parts by weight thermoplastic binder and, correspondingly, from about 70 to 20 parts by weight magnetically responsive material, and ~b) a surface treatment composition comprising from about 0.1 to 2 parts by weight fluoro-aliphatic compound per 100 parts by weight of said particles, s~aid surface treatment composition being attached to the surface of said particles, thereby adhering said toner powder to said electrostatic image area and thereby develop-ing said electrostatic image area; and fixing said toner powder by means of heat, pressure, or heat and pressure.
According to a further aspect of the present invention there is provided a process of preparing a one-part flowable, dry, electrostatically attractable toner powder comprising: providing a pluTality of particles each ~0 comprising a blend of from about 30 to 80 parts by weight thermoplastic binder and, correspondingly, from about 70 to 20 parts by weight magnetically respon-sive material; providing a surface treatment composition comprising from about 0.1 to 2 parts by weight fluoroaliphatic compound per 100 parts by weight of said particles; mixing said particles and said surface treatment composition together at a ten~erature less than the softening point of said thermoplastic binder for a time sufficient to at least loosely attach said surface treatment composition to the surface of said particles; heating said particles with at-P~

1 1~809() tached surface treatment composition to a temperature of about the glasstransitioll temperature of said thermoplastic binder with continued mixing;
and maintaining said heating with continued mixing ~or a time su~ficient to substantially permanently attach said surface treatment composition to said particles as a layer at or near the outer surface of said particles, thereby providing said toner composition.
The toner powder o the present invention produced ~inal images with sharply defined edges, substantially reduced "fuzzy fill-in'1, and substan-tially reduced background, even in the areas between images. The most preferred toner of the invention virtually eliminates "fuzzy fill-in", and background!
Additionally, the toner of the invention possesses improved flow properties in high humidity conditions. Thus, it does not significantly cake or clump under suel~ conditions and the images produced therefrom have sharp edge definition~
e~hibit reduced "fuzzy fill-in", and reduced background.
Still further, the toner powder of the invention tends to be less sensitive to changes in the size of the developing gap utilized than are the previously known one-part toners. Thus, there generally is less decrease in image density as the gap is widened with the instant toners than with such prior art toners. This permits the use of more generous process conditions and machine ~0 tolerc~nces, such as doctor blade gap, may be relaxed. The toner of the invention also permits the use of smooth surface developer rolls in place of the more ex-pensive rough surface developer rolls.
The toner powder of the invention also possessess a less positive triboelectric characteristic than does a correspondingly non-surface treated toner powder. It is believed that this property accounts at least in part for the ability of the developing powder compositions of the invention to provide such high resolution images.

~4a-~1~81~

Det~iled Descri~tion of the Invent;on The po~der of the present invention preferably comprises essen-tially spherical particles wherein at least 95 number percent of the particles have a maximum dimension in the range of about 4 to 30 microns. Preferably -4b-~, .~ .

the particles each comprise a blend of from about 35 to 45 ~arts by weight thermoplastic binder, and correspondingly, from about 65 to 55 parts by weight .~agnetically respon-sive material. Most pre~erably the particles each com-prise a homogeneous blend of the binder and magneticallyresponsive material.
The surprising improvements in copy quality obtained by using the toner powder oE the invention is the result or treating the surface thereof so that the treat-ment composition is attached to the surface of theindividual particles. Although the exact mechanism of attachment is not completely understood, it is believed that attachment is achieved by at least partially embedding the mixture into the surface of the particles to provide a layer or zone of the treatment around the particles.
The fluoroaliphatic compound useful as the surface treatment composition may be monomeric or polymeric and, preferably, contains in the same molecule both a fluoroaliphatic group and a group which may contain an aliphatic group, an aromatic group, or both and which is attracted to the thermoplastic binder used in the toner powder of the invention. The particular structure of the fluoroaliphatic compound is not critical to the invention.
However, the preferred fluoroaliphatic compound may be represented as RfQm2 where R~ is a fluoroaliphatic group, ~m is a linking group, and Z is a terminal group.
The fluoroaliphatic group, may be generally described as a fluorinated, monovalent, non-aromatic group

3 of at least 3 carbon atoms. The alphatic chain may be saturated, unsaturated, straight, branched, or, if sufficiently large, cyclic and may include oxygen or trivalent nitrogen atoms bonded only to carbon atoms. A
fully luorinated group is preferred, but hydrogen or chlorine atoms may be present as .substituents provided that not more than one atom of either is present for every two carbon atoms, and preferably, the group contains at ` 11~80~() least a terminal perfluoromethyl group. While fluoro-aliphatic groups containing a larger number of carbon atoms will function adequately, tho~e containing not more ~han about 20 car~on a~oms are preferLed since larger groups usually represent a less efficient utilization of fluorine than is possible with shorter chains. Fluoro-aliphatic groups containing about 5 to 12 carbon atoms are most preferred.
In the linking group Qm~ m is an integer ~rom 0 to 2, and Q represents a direct bond between Rf and Z when m is zero, or a multifunctional, generally difunctional, linking group such as alkylene, arylene, sulfonamido alkylene, carbonamido alkylene and the like. In some instances more than one R~ group may attach to a single Q
group and in other instances, a single Rf group may be linked to more than one Q group, or may be linked by a single Q group to more than one Z group.
The Z groùp represen~s an anionic, a cationic, a non-ionic or an ampholytic moiety or combinations thereof.
Typical anionic groups would include -CO2M, -SO2M~ -SO3~, -OPOOM, and -OP(OM)2, where M is hydrogen or a metallic ion, such as sodium, potassium, calcium, etc. Typical cationic groups would include -NH2, -NHR, where R is a lower alkyl group such as methyl, ethyl or butyl, -NR3~A~, where Rl is a lower alkyl group or hydrogen and A is an anion, such as iodide, chloride, sulphate, phosphate, hydride, etc. Typical non-ionic groups would include -NR2-~0 and those derived from polyethylene oxide and mixed polye~hylene oxide-polypropylene oxide polyols.
3 Typical mixed or ampholytic groups would include -N(C2H4OH)2~ -N~C2H4NHC2H4NH2~ -N(cH3)2c2H
-N(CH3)(C2H4CO2H)2 -~ O, and the like.
Specific examples of useful ~luoroaliphatic compounds include C8F17Sa2N ( C2H5 ) C2H40CoNH~$1 C8F17S2N ~ C2H5 ) C2H40CONH

., ~

~ 1580g() ~C8~l7so?NHc3Hs~(cH3)3)I3 C8~17S2N(C~3)H

C8F17S2N ( C2H5 ) CH2COOH

Cg~l7SO2NHC2H4NHC2H4NH2 (cgFl7so2N(c~Hs)c2H4o)2pooH

C8Fl7so2w(c2Hs)c2H~opo(oH)2 Other specific examples of useful fluoroaliphatic compounds include CF3C(C2Fs)2C(CF3)-C(CF3)O - ~ SO3M

where M is as described above, available as "MD 31" from ICI, Ltd., (CaF2a+1C2H4O)2P(o)(ONH~), where a is an integer of from A about 5-25, available as "Zony ~ FSP from E. I. duPont deNemours), and CaF2a+lC2H4SCIHCOOM
CH2COOM,~where a and M are as described above available as "Lodyne~ S100 from Ciba-Geigy.
Polymeric fluoroaliphatic compounds are also useful in the invention. For example, the copolymer (95/5 by weight) of CgF17SO2N(C2Hs)C2HsOCOC(CH3~-CH2 and butylacrylate is a useful surface treatment material.
Fluoroaliphatic compounds and methods for their preparation are further described in, for example, United States Patents, 2,559,751; 2,559,749, 2,559,754;
2,559,629; 2,597,702; 2,732,398; 2,759,019; 2,803,615;
f~,o~e ~)~1L

1 lssosn 2,80~,999; ~,915,554; 3,129,254; 3,282,905; 3,39~,182;
3,911,0So; 4,171,282; British Speciications 1,270,662, 1,130,822, and Organic Fluorine Chemis~ry, L~lilas Hudlicky, Plenum Press, ~.Y. (1971).
The fluoroaliphatic compound is preferably blended with one or more other ingredients before being applied to the surface of the particles. Thus, the surface treatment may further comprise from about 0.1 to 2.5, preferably 0.5 to 2.5, parts by weight silicon dioxide per 100 parts by weight particles; from about 0.1 to 2, preferably 0.5 to 1, parts by weight carbon per 100 parts by weight particles; or both.
~lost preferably the treatment composition comprises a mixture of said fluoroaliphatic compound, said silicon dioxide, and said carbon. In ~his instance the treatment composition preferably comprises from about 0.
to 1 part by weight silicon dioxide, 0.4 to 0.7 part by weight fluoroaliphatic compound, and 0.7 to 0.8 part by weight carbon per 100 parts by weight particles when heat-fusing toners are made; and from about 1 to 2.5 parts by weight silicon dioxide, 0.6 to 1.2 parts by weight fluoroaliphatic compound, and 0.7 to 0.8 part by weight carbon per 100 parts by weight particles when pressure-fixing toners are made.
The silicon dioxide useful in the surface treat-ment comprises a powder having an average particle size (i.e., average diameter) smaller than that of the toner powder particles but whose exact size is otherwise not critical to the invention. Preferably the silicon dioxide is a pyrogenic silica in the form of spherical particles having an average diameter in the range of 5 to 50 milli-microns (most preferably in the range of 10 to 20 milli-microns).
Silicon dioxide particles per se are known and may be prepared by, for example, the hydrolysis o~ silicon tetrachloride in an oxygen-hydrogen flame. Py~ogenic silicon dioxide is hydrophilic as prepared. However, it ~ 1~809~
g can be rendered hydrophobic, if desired, by reacting the silanol groues on tne particle surface with chlorosilane.
E~amples of use~ul silicon dioxides include "~erosil~" 20C (a hydrophilic, pyrogenic, white fluffy powder, 99.8% SiO~, average primary particle si~e o, 12 millimicron, bulk density of 200 m2/g, and BET surface area of ~00 ~ 25 m2/G), and "AerosilO" R972 (a hydro-phobic, pyrogenic, white fluffy powder, 98.3% SiO2, average primary particle size of 16 millimicron, bulk density of 60 g/1, and BET surface area of 120 ~ 20 m2/g).
These materials are available from Degussa, Incorporated.
The carbon useful in the surface treatment i5 also a powder whose average particle size (i.e., average diameter~ is smaller than that of the toner powder particles but whose exact size is otherwise not critical to the invention. Particularly useful carbons have an average diameter below about lO0 millimicrons and preferably one below about 40 millimicrons. It is also preferred that the carbon be conductive, i.e., that it have a static electrical conductivity of at least 10-2 reciprocal ohm-cm in a 10,000 v/cm electrical ield.
Static electrical conductivity may be measured as described in U.S. Patent 3,639,245 at column 3, line 47 -column 6, line 46.
E~amples of useful carbon materials include A carbon blacks such as "Vulcan~ XC-72R, a conductive carbon black with a maximum particle size of 30 millimicron sold by Cabot Corporation; "Conducte~" 9S0, maximum particle si~e of 21 millimicron sold by Cities Service; "Rave 1800, maximum particle size of 1~ millimicron sold by Columbia ~hemicals; "Ketjenblackr' EC sold by Noury; and "Thermax" MT sold by R. T. Vanderbilt.
When a conductive carbon is employed in the surface treatment, the resulting ton~r powder preferably has a dynamic conductivity in the range of 2-15 (most preferably 6-9) microamperes (~A) in an electric field of 1,000 D.C. volts. The dynamic conductivity referred to t~d~e ~

..

t 1580g() here is measured according to the technique described hereinafter.
~ he thermoplastic binder useful in the present inven~io~ may be any thermoplastic material although or~anic materials are preferred. ~ost preferably the binder is selected from the group consisting of ~a) waxes that have a melting point in the range of 45C to 150C as measured according to ASTM:D-127, (b) organic resins that have a ring and ball softening point above about 60C as measured according to AST~:E-128, and mixtures of the two.
Waxes useful in the binder include aliphatic waxes (e.g., natural or synthetic), fatty acids and derivatives thereof, metal salts of fatty acids, hydroxylated fatty acids or amides, low molecular weight ethylene homopolymers, or mixtures of such materials.
Other useful waxes include aromatic and polymeric wax~ e materials.
Representative examples of useful aliphatic waxes include paraffin wax, microcrystalline wax, caranauba wax, montan wax, ouricury wax, ceresin wax, candellila wax, and sugar cane wax. Representative examples of useful fatty acids include stearic acid, palmitic acid, and behenic acid. Representative examples of useful metal salts of fatty acids include aluminum stearate, lead stearate, barium stearate, magnesium stearate, zinc stearate, lithium stearate, and zinc palmitate. Representative examples of useful fatty acid derivatives include castor wax (glyceryl tris-12-hydroxy stearate), methyl hydroxystearate (commercially avaiIable A 30 under the trade name "Paracin~l"), ethylene glycol monohydroxy stearate (commercially availabIe under the trade name ~Paracin 15"), and hydroxystearic acid.
Representative examples of useful hydroxylated fatty acids or amides include N(betahydroxyethyl)ricinoleamide (commercially available under the trade name "Flexricin 115"), N,N'ethylene-bis-ricinoleamide (commercially available under the trade name "Flexricin 185"), L158~

N(2-hydroxylethyl)~12-hydroxystearami~e (commercially available under the trade name "Paracin 220"), and N,N'-ethylene-bis-12-hydroxystearamide (commercially available under ~h~ trade name "Paracin 285").
Representative examples of ethylene homopolymers include the low molecular weight polvyethylenes such as the Bareco "Polywaxes", e.g., "Polywax~ 655, 1000, and 2000 sold by the Bareco Division of Petrolite Corporation. Other ~thylene homopolymers include oxidized, high density, low molecular weight polyethylenes such as "Polywax" E-2018 and E-2020 sold by Bar~eco Division oE Petrolite Corpora-tion, and the "Epolene~' series of low molecular weight polyethylene resins such as "Epolene" E-14 available ~rom Eastman Chemical Products Incorporated. Representative examples of useful aromatic wax-lilce materials include dicyclohexylphthalate, diphenylphthalate and the "Be S~uar~ series of waxes from thè Bareco Division of Petrolite Corporation, such as "Be Square" 195. The "8e~
Square" waxes are high melting point waxes that consist of paraffins and napthenic hydrocarbons.
Representative organic resins useful as the thermoplastic binder are polyamides, polystyrenes (e.g., 2000 mol. wt.); epoxy resins (e.g.l diglycidyl ether of bisphenol-A such as "Epon~' 1004, commercially available ~5 from Shel~ Chemical Corp); acrylic resins (e.g., "Elvacite 2044, and N-butyl methacrylate commercially available from E. I. duPont deNemours); vinyl resins such as polyvinyl butyral (e.g., "~utva~" ~72-A, commercially available fro~ Monsanto Company), polyvinyl acetate resins 3 ~e.g., "Gelva~' V-100, commercially available from Monsanto Company); vinyl copo~ymers such as vinyl chloride/vinyl acetate (e.g., "VY~H', commercially available from Union Carbide Corp.), ethylene/vinyl acetate copolymersi cellulose esters such as cellulose acetate butyrate (e.g., nEAB-171-25", commercialiy available from Eastman Ch~mical Products, Inc.), cellulose acetate propionate; and cellulose ethers.
t~

11~8~gn When a heat-fusible developing powder is desired, the thermopla~tic binder preferably comprises the organic resin. Most preferably the organic resin is an epoxy resin. However, some wax may also be incorporated into the binder of a heat-fusible toner powder. The wax is added to reduce the temperature necessary to achieve satisfactory fusing of the toner to a desired surface.
Typically the weight ratio of the organic resin to the wax is between about 4:1 and 20:1.
When a pressure fixable developing powder is prepared, the thermoplastic binder comprises either the wax alone or a combination of the wax and the organic resin. When the binder comprises said combination~ the weight ratio of wax to organic resin is between about 1:1 to 50:1, preferably between about 4:1 and 20:1. Most preferably the binder consists essentially of the wax. In either event, the wax preferably is selected from micro-crystalline wax, low molecular weigh~ polyethylene resin, or a combination thereof, while the organic resin, when present, comprises an epoxy resin.
The magnetically responsive material employed in the developing powder composition preferably is homo-geneously distributed throughout the binder. Addition-ally, it preferably has an average major dimension of one micron or less. Representative examples of useful magnetically responsive materials include magnetite, barium ~errite, nickel zinc ferrite, chromium ox~de, nickel oxide, etc.
Other binders useful for pressure-fixable ton~r powders are known. Thus, for example, see U. S. Patent 3,965,022. This patent describes a binder that comprises (a) about 74 to 98 parts by volume of a thermoplastic component that has a softening point of at least about 60C, a 10-second shear creep compliance in the range of about 1 x 10-9 cm2/dyne to 1 x 10-13 cm2/dyne at room temperature, and a "heat deflection temperature" below about 300C, and (b) about 2 to 26 parts by volume of a 5 8 ~

non-volatile component having a principal glass transition temperature below about 0C as measured by differential thermal analysis, and a 10-second shear creep compliance in the range of about 50 cm2/dyne to 8 x 10 8 cm2/dyne at room temperature, said non-volatile component preferably being elastomeric.
Examples of useful -thermoplastic components (i.e., low shear creep compliance materials) and of non-volatile components (i.e., high shear creep compliance materials) are disclosed in U.S. 3,965,022.
Other ingredients may be incorporated onto the particles used in the toner powder of the invention.
Thus, fatty acid amides containing at least about 10 carbon atoms have been found to be useful in reducing the time required to prepare the toner powders. Typically from about 0.05 to 2~ ~y weight of the fatty acid amide is satisfactory. Examples of useful fatty acid amides include erucamide, stearamide, behenamide, oleamide, N,N'-ethylene-bis(tall oil)amide, and N,N'-ethylene-bis-oleamide.
The developing powders of the invention may be readily prepared. Thus, a dry blend of the thermoplastic binder and the magnetically responsive material is obtained by melting the thermoplastic binder, stirring in the magnetically responsive material, preferably until a homogeneous mixture is provided, allowing the mixture to cool, grinding the mixture to form particles, and classifying the resulting solid particles to the desired si2e (i.e., 1 to 40 microns maximum dimension).
The particles, which are irregularly shaped, are then preferably formed into "prespheres" by first aspirating them into a moving gas stream, preferably air, thus creating an aerosol, and directing the aerosol at an angle of about 90 * 5 through a stream of gas, again preferably air, which has been heated to about 450C and 1 ~580~n 600C into a cooling chamber where the now substantially spherical particles settle by gravity as they cool.
The surface treatment composition is then applied to the "prespheres". ~hen the ~reattnent composi-tion contains ingredients (e.g., silicon dioxide and/orcarbon) other than the fluoroaliphatic compound, a mixture of the ingredients is first prepared by charging them to, for example, a "Warin~" blender and mixing for about one-half hour at a medium speed. The resulting preferably homogeneous mixture is fluffy and black.
The prespheres and surface treatment composition are then each added to a blenvder te.g., a twin shell blender Erom "Patterson Kell~") and cold blended a temperature less than the softening point of the thermo-plastic binder (e.g., 2~-30C) until the surface treatment is at least loosely adhered to the prespheres. Typically this is accomplished within three hours. I~ desired, the prespheres may be cold blended with one of the above disclosed fatty acid amides before treating the prespheres with the surface treatment composition.
In either event, the treated prespheres are then "hot7' blended at about the glass transition tamperature of the thermoplastic binder for a time sufficient to substantially permanently attach the treatment composition ~5 to the particles. This is typically accomplished in from two to six hours. Preferably the surface treatment composition is attached as a layer or ~one at or near the surface of the prespheres.
After hot blending, the resultant toner powder is cooled for about one half hour, screened to remove agglomerates, and classified so that 95% by weight of the product is greater than 4 microns average diameter and only 5% by weight is greater than 30 microns average diameter.
The toner powder of the invention is useful in electrographic recording processes where a differential image pattern of the toner is formed and subsequently ,~ P ,6~

1 1~80~n fixed by means oE pressure, heat, or heat and pressure.
The diferential image pat~ern may be formed by, for example, forming electrostatic image areas on a photocon-ductive surface ad contacting the image areas with the toner. Alternatively, the differential image pat~ern may be formed by contacting a passive dielectric su~face with the toner; forming the image pattern by, for example, selectively exposing the uniformly toned surface to a stylus which imagewise transmits an electrical potential signal; and magnetically removing toner from uncharged areas. See U.S. Patent 3,816,840 for further description of this process. If desired, the toned image areas may be transferred to another surface prior to fixing.
The present invention is further illustrated by means of the following examples wherein the term "parts"
refers to parts by weight unless otherwise indicated.
In these examples, several physical character-istics of the toner powders were measured. The techniques for measuring these characteristics are described below.
a. Dynamic Conductivity.
This property simulates the electrical conductivity of a toner powder when used in an electro-static copying process. Dynamic conductivity is measured on a test rig t~ at comprises the developing station o~ a A 25 "Secretary III photocopier (available from the 3M
Company) except that the photoconductor drum is replaced by an aluminum drum (12.5 cm dia). The developer roll comprises a stainless steel shell (3.15 cm dia) around an 8 pole circular magnet. ~ doctor blade, a toner hopper, and a lO00 volt power supply are also supplied. The gap between the developer roll and the aluminum drum is set at 0.071 cm, the gap between the doctor blade and the toner hopper at 0.05 cm; and the gap between the toner hopper and the developer roll at 0.125 cm.
To measure conductivity, 16 ml of toner is charged to the hopper, and the test rig is started so that the developer roll and the aluminum drum are driven in f~Zd J~

1 1~8U9() opposing directions with tne developer roll having a sur'ace speed of 61.3 cm/sec and the aluminum drum having a surface speed of 19.5 cm/sec. The test rig is then run for five minutes aft~r which the current passing through toner is measured while the toner is in the development gap and under a 1000 volt potential.
b. ~aximum Dengity (Dmax) This property illustrates the optical output density of an image produced from an original having an optical input density of one. Preferably DmaX is at least one.
~ max is measured by determining the diffuse reflection optical density of the image using a conven-tional diffuse reflection densitometer (e.g., Mac~eth Quanta-Log Diffuse Reflection Densitometer, Model RD-100).
The optical density reading is taken as the DmaX for the toner powder being tested.
c. Density Decay.
This property measures the sensitivity of a toner powder to changes in the size of the development gap. Generally speaking, the density of an image produced from a given toner powder decreases as the siæe of the development gap increases. Thus the larger the gap, the lower the resultant image density. Larger decreases indicate that the toner powder is more sensitive to such changes and, therefore, requires narrower development gaps.
Density decay is measured on a conventional electrographic recording device (e.g., a "Secretary III") as follows. The development gap is reduced to the point at which image densities on an imaged and developed photoconductive surface vary from bands of high and low image density horizontally across said photoconductive surface. The development gap is then opened by turning the adjustment means two full turns from this point. A
copy is produced at this opening and its image density measured using a conventional diffuse reflection densi-0~1~

tometer such as is set Eorth above. The development gap is then ~urther opened by turning the adjustment means ~our additional (to~al o~ six) turns ~rom said point. A
copy is produced at this opening and its image density measured as described above~ The density decay i3 taken as the decrease in image density from the narrower ko the wider o the two development gaps.
d. Contrast (Gamma).
This property is a measure of a toner powder's ability to distinguish between dif~ering image densities on an original and reproduce those differences on a copy.
High contrast values, i.e., greater than 5, indicate the toner powder's inability to distinguish and reproduce the difference between varying image densities.
Contrast is measured according to the following procedure. Copies of an original haviny a range of image densities (i.e., a step wedge) are made on an electro-graphic recording (e.g., a "Secretary III") machine. The output image densities are measured as described above in the DmaX test and plotted against the loglo of the input image densities. The loglo of the input densities are plotted as the horizontal axis and the output densities are plotted as the vertical axis. The contrast (gamma) is taken as the slope of the straight line portion of the plot.

Examples 1-16 A series of examples of heat fusible toner powders were prepared. In the examples, 95% by weight of the toner powders were greater than 5 microns average diameter and only 5% by weight were greater than 22 microns average diameter. Examples 1-15 were examples of the invention while Example 16 was a toner powder that was not surface treated.
In each example the prespheres were prepared as described above from 40 parts epoxy resin ("Epon" 1004 ~rom Shell Chemical Company) and 60 parts magnetite.

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Examples l-i~ the prespheres were separately surface treated as described above using different treatment cvmpositions. In example 15 the surface traatment composition ~as cold blended with the prespheres for 15 5 hours prior to hot blending.
The following treatment compositions, with quantities reported as parts, were used:

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~20-The non-surace treated toner powder (Example 1~) was prepared by combining 100 parts o~ the prespheres with 0.6 parts o~ conductive carbon black (Vulcan XC-72R
Erom tAe Cabot Corporation) to form a mixture. The mixture was dry blended at room temperature ~or 3 hours and then hot blended at 65C for about 8 hours. The carbon was then embedded into the prespheres as a layer or ~one at or near the surEace thereof by drawing the particles of the mixture into an air stream at a rate of 36 kg/hr to form an aerosol; directing the aerosol at 90 + 5 into a hot (650C) air stream; allowing the powder to settle; and collectiny the powder by filtration.
About 0.05% by weight SiO2 ("Aerosil" 372, Degussa, Incorporated) was blended with the toner as a separate component to aid its flow properties.
The powders were then used in a heat-fusing copying process in a "Secretary III" copying machine (available from the 3M Company) to provide images on plain paper substrates. The exposure vol~ages are reported in Table 1. The bias voltage was set at -200 DC volts.
The ~urface treatment compositions employed together with the results obtained (i.e., dynamic conductivity of the toner powders, the maximum density (DmaX)~ the density decay, and the image contrast) are given in Table 1.

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1 1~8~9n The toner powders of the invention, i.e., those used in Examples 1-15 provided copies with images that were more sharply defined than were the images provided by ,he toner us~d in Example 16. T'nus the edges o~ the images produced in Examples 1-15 were sharp, ~he openings in the images (letters) had substantially reduced "fuzzy fill-in", and the spaces between the images (background) had substantially reduced blurring caused by undesired toner deposition. Furthermore, the toners used in Examples 1, 2, 7, and 13 produced copies having virtually no "fuzzy fill-in" and virtually no background. The images produced from the toner used in Example 1~, however, had blurry edges, substantial "fuzæy fill-in", and substantial ~ackground.
Additionally, the toners of the invention generally demonstrated less density decay than did the non-surface treated toner used in Example 16. Thus, the toners of the invention generally permit the use of less stringent process conditions such as yap latitude.
The foregoing results are achieved without adversely affecting other physical characteristics of the toner powders. Thus, dynamic conductivity, Dma~, and contrast all remain within acceptable limits.

A pressure-fixable toner powder according to the invention was prepared as described above except that the prespheres were prepared Erom 10 parts "Polywax" 1000 (a low molecular weight, unmodified homopolymer of ethylene having a Mw/Mm of 1.2 from Bareco Division of Petrolite 3 Corporation), 30 parts "Epolene" E-14 (an emulsifiable low molecular weight polyethylene resin from Eastman Chemical Products, Incorporated), and 60 parts Magnetite.
The prespheres were surface treated as described above with a treatment composition comprising 0.6 parts nVulcan" XC-72R, 2.4 parts "Aerosil" 200~ and 1.2 parts C8F17S2N(C2Hs)CH~CH-l ~80g(1 The resulting toner powder ~as used in a cold(room temperature) pr~ssure-fixing copying process to provide images on a plain paper substrate. The exposure voltage was ~ volts. The images on the copie~ produced

5 were sharp, the openings in the images had virtually no "fuzzy fill-in", and there was virtually no background.
The toner powder had a dynamic conduc~ivity of 5.3 A/103V, a Dma~ f 1.47, and a contrast (gamma) of 4.3.

A heat-fusible toner powder according to the invention was prepared as described in Examples 1-14 utilizing the following surface treatment composition:
CgF17SO2NHC2~4~HC2~4NH2 0.6 parts "Aerosil" 200 0.8 parts "Vulcan" XC-72R 0.7 parts The resulting toner powder was used in a heat-fusing copying process in a "Secretary" III copying machine to provide images on plain paper substrates. The exposure voltage was 75 volts and the bias voltage was 200 volts.
The images on the resultant copy were sharply defined, had virtually no "fuzzy fill-in", and the copy had virtually no background. Additionally, the toner powder had a dynamic conductivity of 9.5 A/103V and produced images having a DmaX f 0.62 and a contrast of 0.65. While the DmaX and contrast values of this example are low, it still demonstrates improved edge sharpness, "fuzzy fill-in" and background.

A heat fusible toner according to the invention was prepared as described in Examples 1-14 except that the surface treatment composition was prepared by the following procedure.
A dispersion of a polymeric fluoroaliphatic - 35 compound in solvent was provided. The fluoroaliphatic Og() ~4-compound was a 95/5 by weight copolymer of C8F17SO2N(C2H5~C2H4OCOC(CH3)=CH2 and butyl acrylate.
Sufficient methyl alcohol was added to the dispersion to ~recipi.at2 the pGlymer. The polymer was dried in a vacuum oven. The fluoroaliphatic compound was then ground with a mortar and pestle to reduce it to a relatively fine powder.
The surface treatment composition was then pre-pared as described above by combining 0.6 part fluoro-chemical, 0.8 part "Aerosil" 200, and 0.7 part "Vulcan"XC-72 R.
The resulting toner powder was used in a heat-fusing copying process in a "Secretary" III copying machine to provide images on plain paper substrate. The exposure voltage was 78 volts and the bias voltage was 200 volts.
The images on on the resultant copy were sharply defined, had virtually no "fuzzy fill-in", and the copy had virtually no background. Additionally, the toner powder had a dynamic conductivity of 8~A/103V and produced images having a DmaX of 0.98 and a contrast of 1.53.

Claims (11)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:

1. A one-part, flowable, dry, electrostatically attractable toner powder comprising (a) particles each comprising a blend of from about 30 to 80 parts by weight thermoplastic binder and, correspondingly from about 70 to 20 parts by weight magnetically responsive material; and (b) a layer of a surface treatment composition attached to each of said particles at or near the outer surface of said particles, said surface treat-ment composition comprising from about 0.1 to 2 parts by weight of a monomeric or polymeric fluoroaliphatic compound per 100 parts by weight of said particles.

2. A toner powder in accordance with claim 1 wherein said surface treat-ment composition further comprises from about 0.1 to 2.5 parts by weight silicon dioxide per 100 parts by weight of said particles, said silicon dioxide having an average diameter smaller than said particles.

3. A toner powder in accordance with claim 1 or 2 wherein said surface treatment composition further comprises from about 0.1 to 2 parts by weight carbon per 100 parts by weight of said particles, said carbon having an average diameter smaller than said particles.

4. A toner powder in accordance with claim 1 wherein said fluoroaliphatic compound contains, within a single molecule, both a fluoroaliphatic group and a group which is attracted to said thermoplastic binder.

5. A toner powder in accordance with claim 4 wherein said fluoroaliphatic compound has the formula RfOmZ where Rf is a fluoroaliphatic group, Z is a term-inal group, and Qm is a linking group joining Rf and Z.

6. A toner powder in accordance with claim 5 wherein said fluoroaliphatic compound is selected from the group where M is hydrogen or a metallic ion, and a is an integer of from 5 to 50.

7. A toner powder according to claim 6 wherein said fluoroaliphatic compound is selected from

8. A method of electrostatographic recording comprising:
forming an electrostatic image pattern on a substrate;
rendering said image pattern visible by contacting it with a one-part, flowable, dry, electrostatically attractable toner powder comprising (a) particles each comprising a blend of from about 30 to 80 parts by weight thermoplastic binder and, correspondingly, from about 70 to 20 parts by weight magnetically responsive material, and (b) layer of a surface treatment composition attached to each of said particles at or near the outer surface of said particles, said treatment composition comprising from about 0.1 to 2 parts by weight fluoroaliphatic compound per 100 parts by weight of said particles thereby adhering said toner powder to said electrostatic image pattern and thereby developing said electrostatic image pattern; and fixing said toner powder by means of heat, pressure, or heat and pressure.

9. A method of electrographic recording comprising:
forming a differential image pattern of a one-part, flowable, dry, electrostatically attractable toner powder comprising (a) particles each comprising a blend of from about 30 to 80 parts by weight thermoplastic binder and, correspondingly, from about 70 to 20 parts by weight magnetically responsive material, and (b) a surface treatment composition comprising from about 0.1 to 2 parts by weight fluoroaliphatic compound per 100 parts by weight of said particles, said surface treatment composition being attached to the surface of said particles, thereby adhering said toner powder to said electrostatic image area and thereby developing said electrostatic image area;
and fixing said toner powder by means of heat, pressure, or heat and pressure.

10 . A process of preparing a one-part flowable, dry, electrostatically attractable toner powder comprising:
providing a plurality of particles each comprising a blend of from about 30 to 80 parts by weight thermoplastic binder and, correspondingly, from about 70 to 20 parts by weight magnetically responsive material;
providing a surface treatment composition comprising from about 0.1 to 2 parts by weight fluoroaliphatic compound per 100 parts by weight of said particles;
mixing said particles and said surface treatment composition together at a temperature less than the softening point of said thermoplastic binder for a time sufficient to at least loosely attach said surface treatment composition to the surface of said particles;
heating said particles with attached surface treatment composition to a temperature of about the glass transition temperature of said thermoplastic binder with continued mixing; and maintaining said heating with continued mixing for a time sufficient to substantially permanently attach said surface treatment composition to said particles as a layer at or near the outer surface of said particles, thereby providing said toner composition.

11. A toner powder in accordance with claim 4 wherein said fluoroaliphatic compound is polymeric.