US3764538A - Electroscopic printing powder - Google Patents
Electroscopic printing powder Download PDFInfo
- Publication number
- US3764538A US3764538A US00123065A US3764538DA US3764538A US 3764538 A US3764538 A US 3764538A US 00123065 A US00123065 A US 00123065A US 3764538D A US3764538D A US 3764538DA US 3764538 A US3764538 A US 3764538A
- Authority
- US
- United States
- Prior art keywords
- resin
- powder
- electroscopic
- centimeters
- percent
- 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.)
- Expired - Lifetime
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- 239000000843 powder Substances 0.000 title claims abstract description 120
- 229920005989 resin Polymers 0.000 claims abstract description 105
- 239000011347 resin Substances 0.000 claims abstract description 105
- 239000000203 mixture Substances 0.000 claims abstract description 95
- 239000002245 particle Substances 0.000 claims abstract description 53
- 229920006122 polyamide resin Polymers 0.000 claims abstract description 34
- 230000000704 physical effect Effects 0.000 claims abstract description 8
- 239000008187 granular material Substances 0.000 claims abstract description 6
- 238000000034 method Methods 0.000 claims description 25
- 238000002844 melting Methods 0.000 claims description 19
- 230000008018 melting Effects 0.000 claims description 18
- 239000000463 material Substances 0.000 claims description 17
- 229920001169 thermoplastic Polymers 0.000 claims description 17
- 239000004416 thermosoftening plastic Substances 0.000 claims description 17
- 150000002148 esters Chemical class 0.000 claims description 16
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 15
- 229930195729 fatty acid Natural products 0.000 claims description 15
- 239000000194 fatty acid Substances 0.000 claims description 15
- -1 polyene fatty acid Chemical class 0.000 claims description 14
- 229920005992 thermoplastic resin Polymers 0.000 claims description 14
- 150000001412 amines Chemical class 0.000 claims description 11
- 238000002156 mixing Methods 0.000 claims description 11
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 10
- 150000005846 sugar alcohols Polymers 0.000 claims description 10
- 239000004952 Polyamide Substances 0.000 claims description 9
- 229920001568 phenolic resin Polymers 0.000 claims description 9
- 229920002647 polyamide Polymers 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 229920006345 thermoplastic polyamide Polymers 0.000 claims description 5
- 230000006872 improvement Effects 0.000 claims description 4
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 claims description 3
- 238000009877 rendering Methods 0.000 claims description 3
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims description 2
- 239000002131 composite material Substances 0.000 claims description 2
- 239000012943 hotmelt Substances 0.000 claims description 2
- 235000020778 linoleic acid Nutrition 0.000 claims description 2
- 239000000155 melt Substances 0.000 abstract description 6
- 239000003086 colorant Substances 0.000 abstract description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 14
- 230000006866 deterioration Effects 0.000 description 9
- 229920005862 polyol Polymers 0.000 description 9
- 150000003077 polyols Chemical class 0.000 description 9
- 239000006229 carbon black Substances 0.000 description 8
- 238000009472 formulation Methods 0.000 description 8
- 239000000049 pigment Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 229910052742 iron Inorganic materials 0.000 description 7
- 239000000975 dye Substances 0.000 description 6
- 229940044600 maleic anhydride Drugs 0.000 description 6
- 238000001228 spectrum Methods 0.000 description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 5
- 230000009471 action Effects 0.000 description 5
- 238000005054 agglomeration Methods 0.000 description 5
- 230000002776 aggregation Effects 0.000 description 5
- 238000000227 grinding Methods 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 235000013350 formula milk Nutrition 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 238000003801 milling Methods 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- CUXYLFPMQMFGPL-UHFFFAOYSA-N (9Z,11E,13E)-9,11,13-Octadecatrienoic acid Natural products CCCCC=CC=CC=CCCCCCCCC(O)=O CUXYLFPMQMFGPL-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 230000009969 flowable effect Effects 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000012815 thermoplastic material Substances 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 1
- OYHQOLUKZRVURQ-UHFFFAOYSA-N 9,12-Octadecadienoic Acid Chemical compound CCCCCC=CCC=CCCCCCCCC(O)=O OYHQOLUKZRVURQ-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- CUXYLFPMQMFGPL-SUTYWZMXSA-N all-trans-octadeca-9,11,13-trienoic acid Chemical compound CCCC\C=C\C=C\C=C\CCCCCCCC(O)=O CUXYLFPMQMFGPL-SUTYWZMXSA-N 0.000 description 1
- CUXYLFPMQMFGPL-FWSDQLJQSA-N alpha-Eleostearic acid Natural products CCCCC=CC=C\C=C\CCCCCCCC(O)=O CUXYLFPMQMFGPL-FWSDQLJQSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000002508 contact lithography Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 238000001739 density measurement Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- IXLCRBHDOFCYRY-UHFFFAOYSA-N dioxido(dioxo)chromium;mercury(2+) Chemical compound [Hg+2].[O-][Cr]([O-])(=O)=O IXLCRBHDOFCYRY-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 235000020610 powder formula Nutrition 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
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
- G03G9/08775—Natural macromolecular compounds or derivatives thereof
-
- 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
- G03G9/08706—Polymers of alkenyl-aromatic compounds
- G03G9/08708—Copolymers of styrene
-
- 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
- G03G9/08742—Binders for toner particles comprising macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/08746—Condensation polymers of aldehydes or ketones
-
- 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
- G03G9/10—Developers with toner particles characterised by carrier 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
- G03G9/10—Developers with toner particles characterised by carrier particles
- G03G9/107—Developers with toner particles characterised by carrier particles having magnetic components
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/001—Electric or magnetic imagery, e.g., xerography, electrography, magnetography, etc. Process, composition, or product
- Y10S430/105—Polymer in developer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/901—Electrodepositable compositions
- Y10S524/902—Electrostatic spray
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/904—Powder coating compositions
Definitions
- 252/62.l X a melt point within the range of 8, whereby devel- 2,940,934 6/1960 Carlson 252/62 1 oped images of substantially improved black density 3,060,051 l0/l962 Johnson et al. 252/62.l X may b f d over d d operating i d 3,093,039 6/1963 Rheinfrank 252/62.l X 3,345,294 10/1967 Cooper 252/62.1 X 15 Claims, No Drawings ELECTROSCOPIC PRINTING POWDER CROSS-REFERENCE TO RELATED APPLICATIONS
- This application is a Continuation of my copending application Ser. No. 692,732, filed Dec. 22, 1967 now abandoned, which in turn is a Continuation-in-Part of the prior copending application Ser. No. 357,743, filed Apr. 6, 1964 now abandoned.
- This invention relates to electroscopic powders of the type useful in rendering visible the latent electrostatic images produced by photoelectrostatic or electrostatic copying. More particularly it relates to improved electroscopic powders for use in automated type photoelectrostaticcopying apparatus.
- an electrostatic charge pattern is created on a charged photoconductive layer, such as zinc oxide or selenium, by exposure to a light pattern.
- a charged photoconductive layer such as zinc oxide or selenium
- Various techniques and devices have been employed to expose the charged surface, such as projection or contact printing methods, fiber optic imaging devices, and various phosphor display devices.
- a latent electrostatic charge image is formed.
- Still other image generating devices are employed that directly deposit a charge pattern corresponding to the graphic subject matter by the use of single or multiple styli.
- the technique of direct imaging may be carried out in the presence of light.
- the technique employed for creating a latent electrostatic charge image it must be rendered visible by development with a suitable resinous, thermoplastic, electroscopic powder and rendered permanent by the application of heat, pressure, solvent vapor or other fixing technique.
- the developed image may be fixed in place on the surface upon which it is formed, or it may be transferred to a new surface and fixed thereon.
- a number of techniques are available and in wide use for carrying out the developing step which brings the electroscopic powder, or toner powder as it is known in the art, into contact with said latent image. These include, for example, powder cascade, powder cloud, and dry magnetic brush development.
- the advancement represented by the improved electroscopic powders of this invention is applicable to all of the foregoing systems where a charge-sensing powder is brought into contact with an electrostatically charged surface for the purpose of producing a visible image.
- the magnetic brush method for developing an electrostatic image involves the use of a mixture of magnetically attractable particles and electroscopic powder. This mixture or developer mix is formed up into a brush-like mass on the surface of a cylindrical roll under the influence of a magnetic field created by magnetic means disposed within said roll.
- the electroscopic powder is held to the magnetically attractable carrier particles by a triboelectric effect which results from frictional contact between the particles. This effect is more fully described in U. S. Pat. No.
- the relative position in the triboelectric series of carrier and electroscopic powder materials will determine the polarity of the charge generated on the electroscopic powder. Hence, particular materials can be selected for either positive or reversal printing.
- the electroscopic powders are mixed with larger carrier particles, such as iron, ferrites, magnetites, cobalt, and nickel.
- the carrier particles align themselves along the lines of magnetic flux provided by the magnetic means so that they stand erect on the surface of the cylinder. In this manner the particles, carrying the electroscopic powder present a uniform and continuous array of developer mix along that portion of the roll which contacts the electrostatic recording member bearing the latent electrostatic image thereon.
- U. S. Pat. No. 3,003,462 discloses a typical magnetic brush development apparatus wherein the developer mix is deposited in a trough, thereafter is picked up on the periphery of an applicating cylinder having the magnetic means therein, and is formed into a brush in the environment of said magnetic field. As the rotating applicator cylinder carries the developer mix outside the magnetic field, the magnetic brush collapses and developer mix falls back into the reservoir. This cycle of brush formation and collapse is repeated as long as the developer roll rotates.
- Electroscopic powders available heretofore have left much to be desired when used in automated electrostatic copying machines, particularly where the magnetic brush-type apparatus is employed.
- One of the major problems is that of deterioration of the electroscopic powder components of the developer mix.
- One evidence of such deterioration appears in the photoelectrostatic copies which begin to show adherence of the electroscopic powder indiscriminately in both image and non-image areas.
- carrier particles may begin to deposit on the copy sheet as a result of mix deterioration giving the photoelectrostatic copy of a gritty feel.
- Still further problems caused by mix deterioration relate to improper mixing and impairment of the mechanical mixing means of the developer apparatus.
- the automated photoelectrostatic office copying equipment under discussion is designed especially for high production, high quality copying. Equipment of this type is required to produce up to 6000 copies in a typical work day. The deteriorated condition referred to above can take place rapidly. Deterioration of known developer mixes has heretofore necessitated complete and frequent replacement with fresh material.
- Deterioration is caused by physical changes in the electroscopic powder. These physical changes primarily concern the particle size of the powder. The first such change relates to particle size fracture or comminution, and the second relates to agglomeration or clumping of small particles into larger ones.
- Electroscopic powder particles may be split or fractured so that the new fragments do not have the same electroscopic properties as the particles from which they were formed. Each of these fragments is present as a spurious particle which serves only to impair the performance of the developer system.
- Agglomeration or clumping is caused by an increase in mix temperature. This temperature rise may be due to the absorption by the powder of frictional energy developed through impact between the particles as they are mixed and churned within the developer unit. Another source of heat is the high temperature fusing unit within the apparatus.
- the thermoplastic toner particles begin to clump or agglomerate as they reach their softening or tackifying temperature. In a severe condition the agglomerates may occlude some of the iron carrier particles. These clumps, containing both iron and softened electroscopic powder, completely disrupt the developing step.
- triboelectric charge on the electroscopic powder depends upon proper contact between toner and carrier particles. Clumping and agglomeration prevent the proper circulation and blending of toner with the carrier in the developer apparatus. A free-flowing condition is particularly necessary during replenishment when fresh toner is added to a depleted mix. Poor circulation gives rise to a non-uniform powder mixture which produces copies that are unevenly developed. Poor blending of electroscopic powder and iron particles reduces the level of triboelectric charge generated on the powder.
- thermosplastic, resinous toner particles must have certain distinct properties if it is to achieve a practical mix life in a magnetic brush developing apparatus.
- the resin blend should be sharp-melting so that it is converted from discrete, solid pieces to a flowable material over a temperature range not greater than about 50 to 8F. Such a resin blend will flow smoothly onto the paper to form a permanent image and solidify rapidly when removed from the fuser, thus producing an image which will not smear.
- the thermosplasticresin should remain in a solid state at temperatures substantially higher than room temperature so that it does not soften, become tacky, and form cakes, clumps, or agglomerates. Such a divergence of requirements demands that the thermosplastic resin be at once tough and resilient enough to withstand the grinding action in the developer apparatus, yet sufficiently brittle and frangible to permit its reduction to powder on conventional grinding equipment.
- thermoplastic compositions which are tough and infrangible, have excellent electroscopic properties, but cannot be manufactured on conventional milling equipment.
- Other resins which may have excellent electroscopic properties and which may be readily ground to a desired particle size in conventional milling equipment are too brittle or frangible for the magnetic brush apparatus. These are reduced to an inordinate amount of dust and fines by the mixing action of the developer unit.
- the electroscopic powders which constitute this invention comprise a blend of a tough, infrangible synthetic resin with a highly frangible thermosplastic synthetic resin which melts between about C. (158F.) and 165C. (329F.), preferably in the range of 2l3235F., said blend having the critical property of going from discrete particles to flowable material in a range from 5-8F.
- the blend of synthetic thermoplastic resin materials preferably should have a correspondingly high softening point, that is, the thermoplastic particles should remain discrete at temperatures up to F. and not adhere to one another or form agglomerates.
- the preferred average particle size of the electroscopic powder ranges from 4 to 10 microns with the over-all range of particle sizes ranging from 1 micron to 74 microns.
- the invention is directed to a novel thermosplastic resinous electroscopic powder comprising a tough, infrangible resin component, such as a thermoplastic polyamide resin, which is chemically blended with a highly frangible, brittle substance such as a rosinmodified maleic anhydride-polyhydric alcohol resin, an unsaturated co-ester resin such as a diphenol resin esterified with a fatty acid, or a pure non-heat reactive phenolic resin.
- a tough, infrangible resin component such as a thermoplastic polyamide resin
- a highly frangible, brittle substance such as a rosinmodified maleic anhydride-polyhydric alcohol resin
- an unsaturated co-ester resin such as a diphenol resin esterified with a fatty acid, or a pure non-heat reactive phenolic resin.
- the powder blends may optionally include additives such as polyol resins, toluenesulfonamides, or butylated-hydroxy-toluene which enter into the blends as fluxing agents, tending to decrease the melt viscosity of the thermoplastic blend.
- additives such as polyol resins, toluenesulfonamides, or butylated-hydroxy-toluene which enter into the blends as fluxing agents, tending to decrease the melt viscosity of the thermoplastic blend.
- the preferred polyamide resins are produced by the reaction of high molecular weight polyene fatty acids and their esters with an amine.
- an amine By reacting ammonia, a primary or secondary amine, a hydroxyamine or an alkanolamine, with a high molecular weight carboxylic acid or an ester thereof, either saturated or unsaturated, said acid or ester being obtainable by polymerizing at elevated temperature said polyene fatty acid or esters thereof, and in the case of the esters, converting the polymers to the corresponding acid if desired, there are produced the preferred polyamides.
- polyene fatty acids in esterified form are 9,1land/or 9,12-octadecadienoic acid (obtainable from soybean oil and dehydrated castor oil), linoleic acid, alpha and beta-eleostearic acid (obtainable from tung oil).
- the preferred esters are those derived from methanol, ethanol, and propanol.
- Primary or secondary amines may be used such as, for example, methylamine, ethylamine, propylamine, ethylenediamine, tetraamethylenediamine, pentamethylenediamine, piperazine, and diethylenetriamine.
- the class of thermoplastic, polyamide resins is disclosed in U. S. Pat. No. 2,379,413 and sold by the General Mills Company under the trademarks Versamide and Omamid. Other suitable polyamide resins are also available from the Krumbhaar Resin Division of Lawter Chemicals, Inc., under the trademark Polymid.
- the second thermoplastic constituent in the electroscopic powder is extremely frangible but it is sharp melting.
- a suitable frangible constituent may be a rosin-modified phenolic resin, such as those prepared by modifying a phenol formaldehyde resin with the reaction product of maleic anhydride and rosin or a polyhydric alcohol such as glycerol or pentaerythrytol.
- rosin-modified phenolic resins are sold under the trademark Amberol" by Rohm & Hass Company.
- Diphenolic resin materials esterified with a soya fatty acid and certain thermoplastic phenolformaldehyde resins exhibit satisfactory frangible properties.
- esterified diphenolics are available from the Johnson Wax Company Chemical Division of Racine, Wisconsin, and the thermoplastic phenol-formaldehyde resins are available from the Krumbhaar Resin Division of Lawter Chemicals, Inc., and from Nelio Chemicals, Inc., Jacksonville, Florida, as their VBR-800 series resins.
- the blend of infrangible and frangible resins with coloring materials forming the electroscopic powder should be highly infrangible and should have a fracturing value of at least 400 grams-centimeters when measured on a wafer of resin 3.75 cm. in diameter and 0.5 cm. in thickness at 100F. by the falling ball method.
- the resin wafer is subjected to impact by a falling ball and the energy (measured in gram-centimeters) required to just fracture the wafer is measured.
- the infrangible resin component of the resin blend should preferably have a fracturing value of at least 1000 gram-centimeters in the foregoing test while the frangible resin component may have low fracturing values in the range of 100-200 gram-centimeters.
- the resin blend forming the electroscopic powder should not soften or become tacky at temperatures below 130F.
- the softening properties of resins can be measured with a penetrometer by the procedure of A.S.T.M. Standard No. D5-61. By this procedure, it has been found that resin blends which permit a maximum penetration not greater than 1.0 millimeter at 130F. with a standard needle (No. 4103) in a standard Lab- Line" penetrometer (No. 4100) at a force of 100 grams for 5 seconds resist softening and do not clump or agglomerate during use as electroscopic powder.
- the action of the fluxing agent is believed to lower the melting point of the blend without broadening the melting point range.
- Successful fluxing agents are provided by the group of polyhydric alcohols sold by the Shell Chemical Company under the trademark "Polyol X-450 of the general formula i al-I5 n FORMULATION NO. 1
- EXAMPLE 1 Electroscopic powder formulation is:
- the quantity of polyamide resin called for is heated in a suitable vessel equipped with a conventional impeller type mixer until the resin is just molten so that it can be stirred.
- To the molten polyamide resin is added the Polyol while the mass is being agitated. Agitation continues during the addition of the maleic anhydridepolyhydric alcohol rosin-modified resin. After the maleic anhydride-polyhydric alochol resin is completely melted, the quantityof black dye is added to the batch followed by the addition of the carbon black.
- the batch After the batch has been thoroughly mixed, it is removed from the mixing vessel, cooled, crushed and pulverized to an average particle size ranging from 4 to 10 microns. Understandably there will be particle sizes ranging from under one micron to 50 microns and larger.
- the electroscopic powder is passed through a 200 mesh screen so that the largest particle size possible in such an electroscopic powder would be under 75 microns.
- the softening point of the electroscopic powder was measured by placing a quantity of the electroscopic powders in a constant temperature oven for 12 hours. A series of oven tests, at different temperature levels, revealed that powder produced in Example I remained in particulate form, and did not clump or agglomerate until tested at a 155F. level.
- the melt point of the electroscopic powder was in the range of 2l5-220F. measured in accordance with A.S.T.M. Method No. E28- 5ST.
- the electroscopic powder was combined with iron particles in a ratio of one part powder to 15 parts iron, making a developer mix suitable for developing electrostatic images.
- the developer mix was charged into the developer unit of a photoelectrostatic copier. More than 50,000 copies were developed with this developer mix requiring the periodic addition of fresh electroscopic powder to replace the amount taken out by the making of copies. Otherwise the developer unit did not require servicing such as complete replacement of the charge, or cleaning of the unit to remove clumps or agglomerates.
- the image copies were of uniform density indicating complete and thorough mixing between the carrier and powder. A high image density was maintained throughout the run while non-image areas maintained clean and free of spurious toner deposition. A copy is considered to have proper image density if reflectance density measurements, taken by a standard Photovoltmeter, are above 1.0 units.
- reflectance readings can give a measure of the contrast between the image and non-image areas.
- the non-image area on a processed copy should not measure more than 0.05 Photovolt units. The copies were clean in the non-image areas giving Photovolt reading less than 0.05 units.
- Polyamide resin (Versamide 930) 74% Maleic anhydride-polyhydric alcohol rosin-modified resin (Amberol 800) l9% Nubian resin black dye 5.6% Carbon black pigment (Neo-spectru, Mark ll) l.4%
- Example 2 The ingredients were processed in accordance with the steps set forth for Example 1 above.
- the melting point range and softening point of the above electroscopic powder were 2l3220F. and greater than 140F., respectively. It will be noted that this example incorporates a major percentage of the tough, infrangible polyamide material. Photovolt readings were all above 1.0 units.
- Such an electroscopic formulation finds particular utility in environments where the copying equipment is used for extended periods of time and where there is a high ambient temperature.
- EXAMPLE 3 An electroscopic powder was prepared in accordance with the procedure of Example 1 wherein the electroscopic powder was comprised largely of polyamide material.
- Polyamide resin (Versamide 930) Maleic anhydride-polyhydric alcohol rosin-modified resin (Amberol 800) 7% Nigrosine dye 6% Polyols 8% Carbon black pigment (Nee-spectra, Mark II) 1%
- the melting point range and the softening point of the granular mass were 217-222F. and greater than F., respectively.
- the formulation of Example 3 is suitable for use under high temperature conditions. The inclusion of a fluxing agent tends to lower the melt point slightly and give a more uniform image.
- Polyamide resin (Versamide 930) 33% Polyol (Shell X-450) fluxing agent 9.9% Phenolic Resin (No. K-254 Krumbhaar Chem. Div. of Lawter Chemicals, Inc.) 49.5% Nubian resin black (National Aniline) 6.6% Carbon black pigment (Nee-spectra, Mark II)
- the above formula has substituted for the maleic anhydride rosin-modified resin a phenol-formaldehyde resin which is a highly frangible, sharp melting thermoplastic material.
- the performance of this formulation in respect of print quality and resistance to developer mix deterioration was fully equivalent to that observed in Example 1.
- the melting point range and softening point of the above example were 21 5-220F. and greater than l40F., respectively.
- EXAMPLE 5 The electroscopic powder prepared in this example conformed to the formula set forth in Example 1 above with the exception that a mixture of orthoand para-N- ethyl-toluene-sulfonamides (Santicizer 8, Monsanto Chemical Company) was substituted as a fluxing agent for the polyol (Shell X450). The copy quality obtained was fully equivalent to the copy quality obtained from the formulation of Example 1.
- EXAMPLE 7 This example differs from Example 1 chiefly in the use of lesser percentages of polyamide resin blended with the highly frangible thermoplastic material. It has been found that the addition of polyamide in amounts less than 9 percent by weight in the electrostatic powder formula has little or no effect on improving its resistance to the grinding and milling action present in the developer apparatus.
- Polyamide resin (Versamide 930) 9% Maleic anhydride-polyhydric alcohol rosin-modified resin (Amberol 800) 83.2% Nubian resin black 6% Carbon black (Nee-spectra, Mark II) 1%
- the above composition had a melting point range and softening point of 220-228F. and above 155F., respectively.
- Electroscopic powders formulated with -6 percent polyamide deteriorated after 3,000-5,000 electrostatic prints. Improvements begin to show when the level of 9 percent, and above, of the polyamide thermoplastic synthetic resin is included in the formula.
- a further advantage of the electroscopic powder of this invention is that it does not agglomerate or cake during storage, and therefore remains uniform, ready for use. It is not uncommon for materials in shipment to be exposed to a wide variety of climatic conditions, including extremely high temperatures, which often cause the powder to actually cake into a solid mass in the shipping container. The material of this invention has been found to retain its free-flowing granular consistency, making it ready for use immediately by the operator.
- the discussion'of the electroscopic powder has been limited to the technique of positive printing wherein the triboelectric relationship of the electroscopic powder to the iron carrier particles is such that the particles acquire the necessary positive charge so that they will adhere to the negatively charged electrostatic image on the photoconductive member.
- the advantages provided by the electroscopic powders of this invention may be applied with equal success to the technique of reversal printing as described in co-pendingapplication Ser. No. 221,888 and assigned to the same assignee.
- a developer mix for use in electrostatic printing to develop latent images including charged and uncharged areas of an image-bearing sheet comprising the combination of a. separate granular triboelectrically chargeable carrier particles, and
- a developer powder comprising 1. a coloring agent selected from the group consisting of dyes and pigments, and
- a resin blend having a triboelectric relationship of opposite polarity with respect to said carrier granules and having a sharp melting point within the range of about C. to about 165 C., said resin blend being formed by mixing the resin components in their molten state and being composed of i. an infrangible thermoplastic polyamide resin formed by reacting a high molecular weight polyene fatty acid or ester thereof with an amine said polyamide resin having a fracturing value of at least 1000 gram centimeters, and
- a highly frangible thermoplastic resin having a fracturing value not greater than 200 gram centimeters, said fracturing values being measured by the falling ball method on a wafer of resin maintained at F. and 3.75 centimeters in diameter and 0.5 centimeters in thickness, whereby developed images of substantially improved density can be formed over extended operating periods.
- a developer mix for use in electrostatic printing to develop latent images including charged and uncharged areas of an image-bearing sheet, said developer mix comprising the combination of a. separate granular magnetically attractable carrier particles, and
- a developer powder comprising 1. a coloring agent selected from the group consisting of dyes and pigments, and
- a resin blend having a triboelectric relationship of opposite polarity with respect to said magnetically attractable granules and having a sharp melting point within the range of about 70C. to about C., said resin blend being formed by mixing the resin components in their molten state and being composed of I i. a major portion of an infrangible thermoplastic polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine, and
- An electroscopic powder suitable for developing electrostatic charge images consisting essentially of frangible and infrangible thermoplastic resins combined when in their molten state to form a miscible mixture, said mixture having physical properties which are distinct from either'of the components comprising said mixture, and having a melting range not greater than 8 F., a softening point not less than 130 F.
- said frangible resin constituting 10 to 91 percent by weight of the electroscopic powder and having a fracturing value not greater than 200 grams centimeters
- said infrangible resin being a polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine and constituting to 90 percent by weight of the electroscopic powder and having a fracturing value of at least 1000 gram centimeters, the fracturing value of the resins being measured at 100 F. by the falling ball method on a wafer of resin 3.75 centimeters in diameter and 0.5 centimeters in thickness.
- the electroscopic powder of claim 4 wherein said powder is comprised of from to 50 percent by weight of said polyamide resin and 50 to 90 percent of a maleicanhydride rosin-modified resin.
- the electroscopic powder of claim 4 wherein said powder is comprised of from 30 to 40 percent polyamide and 40 to 50 percent maleic anhydride rosinmodified resin and from 1 to 10 percent polyhydric alcohol fluxing agents.
- thermoplastic infrangible polyamide resin from 50 to 90 percent of said thermoplastic infrangible polyamide resin and from 5 to 40 percent of a frangible thermoplastic resin component selected from the group consisting of maleic anhydride rosin-modified resin, esterified diphenolic resin, and phenol-formaldehyde resins.
- the electroscopic powder of claim 4 wherein said powder has a particle size range of from 1 micron to 74 microns with an average particle size of from 4 microns to 10 microns.
- a developer mix for use with magnetic brushtype developing apparatus for rendering latent electrostatic charge images visible on electrostatic recording members by applying thereto an electroscopic powder, and subsequently fixing the adhered powder thereto said developer mix comprising a granular electroscopic powder of colored thermoplastic particles mixed with larger magnetically attractable carrier particles each having a charge of opposite polarity, said thermoplastic powder having as one component a polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine heat blended with a second frangible resin component to form a composite electroscopic powder having a fracturing value of at least 400 gram centimeters and said polyamide resin having a fracturing value of at least 1000 gram centimeters.
- the second component is maleic-anhydridepolyhydricalcohol rosin-modified resin in an amount of from 9 to 50 percent by weight of the electroscopic powder.
- the developer mix as claimed in claim 11 wherein the polyamide resin is a reaction product of polymerized linoleic acid and ethylenediamine.
- the developer mix as claimed in claim 10 wherein the electroscopic powder has an average particle size in the range of from 4 microns to 10 microns.
- An improved electrostatic developer mix including carrier particles and colored toner particles, wherein the improvement comprises said toner particles being a hot melt blend of an infrangible thermoplastic resin and a frangible thermoplastic resin wherein physical properties of the resulting blend are distinct from the properties of either of the separate components, said infrangible resin material being a polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine said polyamide resin having a fracturing value of at least 1000 gram centimeters and said frangible material having a fracturing value less than 200 gram centimeters and the fracturing of the blend being at least 400 gram centimeters.
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Abstract
A developer mix for use in electrostatic printing to develop latent images, including charged and uncharged areas of an image bearing sheet said developer mix comprising separate granular carrier particles, and a developer powder comprising a coloring agent and a resin having a triboelectric relationship of opposite polarity with respect to said carrier granules, said resin comprising a blend of resins in which the physical properties of the blend are distinct with respect to the physical properties of the resin components which are heat blended together, the principal resin being a polyamide resin which represents the infrangible resin component, and the completed resin being reduced to a melt point within the range of 8*, whereby developed images of substantially improved black density may be formed over extended operating periods.
Description
O United States Patent [191 1111 3,764,538
Shelffo Oct. 9, 1973 [54] ELECTROSCOPIC PRINTING POWDER 2,867,592 1/1959 Morris et al. 260/18 PN 1 new Loren Show Palatine, 533333 131322 22352335.: .113: 328112 1 2 [73] Assignee: Addressograph-Multigraph Corporation, Cleveland, Ohio Primary Examiner-Norman G. Torchin Assistant Examiner-J. P. Brammer [22] Filed 1971 Att0rneyS0l L. Goldstein [21] Appl. No.: 123,065
Related U.S. Application Data ABSTRACT [63] Continuation of Ser. No. 692,732, Dec. 22, 1967, A developer mix for use in electrostatic printing to den n h h is a n in i n-in-p r f Sen velop latent images, including charged and uncharged 357,743. P" 1 1964, abandoned areas of an image bearing sheet said developer mix comprising separate granular carrier particles, and a [52] U.S. Cl 252/62.1, 260/18, 260/19 developer der comprising a coloring agent and a [51] Int. Cl G03g 9/02 resin having a triboeieciric relationship f opposite [58] Field of Search 252/62.1; 260/18, polarity with respect to Said carrier granules, Said resin 260/18 19 comprising a blend of resins in which the physical properties of the blend are distinct with respect to the [56] References Cited physical properties of the resin components which are UNITED STATES PATENTS heat blended together, the principal resin being a 2,221,776 11 1940 Carlson 252/62.1 x Polyamide resin'whieh represents the infrangible resin 2,297,691 10/1942 Carlson 252/62.1 x mp n nt, an th mpleted resin being reduced to 2,899,335 8/1959 Straughan... 252/62.l X a melt point within the range of 8, whereby devel- 2,940,934 6/1960 Carlson 252/62 1 oped images of substantially improved black density 3,060,051 l0/l962 Johnson et al. 252/62.l X may b f d over d d operating i d 3,093,039 6/1963 Rheinfrank 252/62.l X 3,345,294 10/1967 Cooper 252/62.1 X 15 Claims, No Drawings ELECTROSCOPIC PRINTING POWDER CROSS-REFERENCE TO RELATED APPLICATIONS This application is a Continuation of my copending application Ser. No. 692,732, filed Dec. 22, 1967 now abandoned, which in turn is a Continuation-in-Part of the prior copending application Ser. No. 357,743, filed Apr. 6, 1964 now abandoned.
This invention relates to electroscopic powders of the type useful in rendering visible the latent electrostatic images produced by photoelectrostatic or electrostatic copying. More particularly it relates to improved electroscopic powders for use in automated type photoelectrostaticcopying apparatus.
In photoelectrostatic copying processes, an electrostatic charge pattern is created on a charged photoconductive layer, such as zinc oxide or selenium, by exposure to a light pattern. Various techniques and devices have been employed to expose the charged surface, such as projection or contact printing methods, fiber optic imaging devices, and various phosphor display devices. Upon exposure of the charged layer to light under darkroom conditions, a latent electrostatic charge image is formed.
Still other image generating devices are employed that directly deposit a charge pattern corresponding to the graphic subject matter by the use of single or multiple styli. The technique of direct imaging may be carried out in the presence of light.
Irrespective of the technique employed for creating a latent electrostatic charge image, it must be rendered visible by development with a suitable resinous, thermoplastic, electroscopic powder and rendered permanent by the application of heat, pressure, solvent vapor or other fixing technique. The developed image may be fixed in place on the surface upon which it is formed, or it may be transferred to a new surface and fixed thereon.
A number of techniques are available and in wide use for carrying out the developing step which brings the electroscopic powder, or toner powder as it is known in the art, into contact with said latent image. These include, for example, powder cascade, powder cloud, and dry magnetic brush development. The advancement represented by the improved electroscopic powders of this invention is applicable to all of the foregoing systems where a charge-sensing powder is brought into contact with an electrostatically charged surface for the purpose of producing a visible image.
Further discussion of the improvements represented by this invention will be explained in terms of the magnetic brush type of apparatus, but the novel electroscopic powders disclosed herein can also be used with equal advantage in other developing apparatus and their use is not limited to magnetic brush technique.
The magnetic brush method for developing an electrostatic image involves the use of a mixture of magnetically attractable particles and electroscopic powder. This mixture or developer mix is formed up into a brush-like mass on the surface of a cylindrical roll under the influence ofa magnetic field created by magnetic means disposed within said roll.
The electroscopic powder is held to the magnetically attractable carrier particles by a triboelectric effect which results from frictional contact between the particles. This effect is more fully described in U. S. Pat. No.
2.874,063 dated Feb. 17, 1959. The relative position in the triboelectric series of carrier and electroscopic powder materials will determine the polarity of the charge generated on the electroscopic powder. Hence, particular materials can be selected for either positive or reversal printing. In practice, the electroscopic powders are mixed with larger carrier particles, such as iron, ferrites, magnetites, cobalt, and nickel. The carrier particles align themselves along the lines of magnetic flux provided by the magnetic means so that they stand erect on the surface of the cylinder. In this manner the particles, carrying the electroscopic powder present a uniform and continuous array of developer mix along that portion of the roll which contacts the electrostatic recording member bearing the latent electrostatic image thereon.
U. S. Pat. No. 3,003,462 discloses a typical magnetic brush development apparatus wherein the developer mix is deposited in a trough, thereafter is picked up on the periphery of an applicating cylinder having the magnetic means therein, and is formed into a brush in the environment of said magnetic field. As the rotating applicator cylinder carries the developer mix outside the magnetic field, the magnetic brush collapses and developer mix falls back into the reservoir. This cycle of brush formation and collapse is repeated as long as the developer roll rotates.
Electroscopic powders available heretofore have left much to be desired when used in automated electrostatic copying machines, particularly where the magnetic brush-type apparatus is employed. One of the major problems is that of deterioration of the electroscopic powder components of the developer mix. One evidence of such deterioration appears in the photoelectrostatic copies which begin to show adherence of the electroscopic powder indiscriminately in both image and non-image areas.
Another evidence of mix deterioration is a fall-off or loss in copy density, that is, the developed image appears gray rather than having an intense black color.
Also, carrier particles may begin to deposit on the copy sheet as a result of mix deterioration giving the photoelectrostatic copy of a gritty feel.
Still further problems caused by mix deterioration relate to improper mixing and impairment of the mechanical mixing means of the developer apparatus.
The automated photoelectrostatic office copying equipment under discussion is designed especially for high production, high quality copying. Equipment of this type is required to produce up to 6000 copies in a typical work day. The deteriorated condition referred to above can take place rapidly. Deterioration of known developer mixes has heretofore necessitated complete and frequent replacement with fresh material.
Deterioration is caused by physical changes in the electroscopic powder. These physical changes primarily concern the particle size of the powder. The first such change relates to particle size fracture or comminution, and the second relates to agglomeration or clumping of small particles into larger ones.
The forces which operate in the magnetic brush developer exert a grinding or milling action on the developer mix. Electroscopic powder particles may be split or fractured so that the new fragments do not have the same electroscopic properties as the particles from which they were formed. Each of these fragments is present as a spurious particle which serves only to impair the performance of the developer system.
Further attrition of the particulate matter generates excessively small particles referred to as dust or fines that are incapable of discriminating between the charged and uncharged areas. These fines tend to become airborne and create an undesirable condition from a housekeeping standpoint.
Agglomeration or clumping is caused by an increase in mix temperature. This temperature rise may be due to the absorption by the powder of frictional energy developed through impact between the particles as they are mixed and churned within the developer unit. Another source of heat is the high temperature fusing unit within the apparatus. The thermoplastic toner particles begin to clump or agglomerate as they reach their softening or tackifying temperature. In a severe condition the agglomerates may occlude some of the iron carrier particles. These clumps, containing both iron and softened electroscopic powder, completely disrupt the developing step.
These clumps often become deposited in clearances between moving and stationary mechanical parts thereby increasing the powder required to drive the magnetic brush roller. The additional power is dissipated as heat so that the process of agglomeration becomes progressively worse.
Generation of the triboelectric charge on the electroscopic powder depends upon proper contact between toner and carrier particles. Clumping and agglomeration prevent the proper circulation and blending of toner with the carrier in the developer apparatus. A free-flowing condition is particularly necessary during replenishment when fresh toner is added to a depleted mix. Poor circulation gives rise to a non-uniform powder mixture which produces copies that are unevenly developed. Poor blending of electroscopic powder and iron particles reduces the level of triboelectric charge generated on the powder.
The demands placed on electroscopic powders suitable for high speed, continuous automatic electrostatic copying, are exacting and have heretofore not been met. From the foregoing discussion, it is seen that the thermosplastic, resinous toner particles must have certain distinct properties if it is to achieve a practical mix life in a magnetic brush developing apparatus.
The resin blend should be sharp-melting so that it is converted from discrete, solid pieces to a flowable material over a temperature range not greater than about 50 to 8F. Such a resin blend will flow smoothly onto the paper to form a permanent image and solidify rapidly when removed from the fuser, thus producing an image which will not smear. The thermosplasticresin should remain in a solid state at temperatures substantially higher than room temperature so that it does not soften, become tacky, and form cakes, clumps, or agglomerates. Such a divergence of requirements demands that the thermosplastic resin be at once tough and resilient enough to withstand the grinding action in the developer apparatus, yet sufficiently brittle and frangible to permit its reduction to powder on conventional grinding equipment.
Some thermoplastic compositions, which are tough and infrangible, have excellent electroscopic properties, but cannot be manufactured on conventional milling equipment. Other resins which may have excellent electroscopic properties and which may be readily ground to a desired particle size in conventional milling equipment are too brittle or frangible for the magnetic brush apparatus. These are reduced to an inordinate amount of dust and fines by the mixing action of the developer unit.
It is a primary object of this invention to provide an electroscopic powder particularly suitable for use in automated and continuous photoelectrostatic copying machines.
It is an object of this invention to provide an electroscopic developing powder having greatly improved resistance to deterioration in magnetic brush developer apparatus.
It is a further object of this invention to provide an electroscopic developing powder that will fuse in a narrow temperature range below the char point of paper and will resist clumping or agglomeration.
It is a further object of this invention to provide electroscopic developing powder which is resistant to attrition or grinding when used in a magnetic brush developer apparatus.
It is a still further object of this invention to provide an electroscopic developing powder comprised of a blend of thermoplastic resins having suitable frangibility properties and temperature response characteristics that will produce consistently high quality electrostatic copies having a high contrast between image and nonimage areas.
These and other objects are apparent from and are achieved in accordance with the following disclosure.
The electroscopic powders which constitute this invention comprise a blend of a tough, infrangible synthetic resin with a highly frangible thermosplastic synthetic resin which melts between about C. (158F.) and 165C. (329F.), preferably in the range of 2l3235F., said blend having the critical property of going from discrete particles to flowable material in a range from 5-8F. The blend of synthetic thermoplastic resin materials preferably should have a correspondingly high softening point, that is, the thermoplastic particles should remain discrete at temperatures up to F. and not adhere to one another or form agglomerates. The preferred average particle size of the electroscopic powder ranges from 4 to 10 microns with the over-all range of particle sizes ranging from 1 micron to 74 microns.
The invention is directed to a novel thermosplastic resinous electroscopic powder comprising a tough, infrangible resin component, such as a thermoplastic polyamide resin, which is chemically blended with a highly frangible, brittle substance such as a rosinmodified maleic anhydride-polyhydric alcohol resin, an unsaturated co-ester resin such as a diphenol resin esterified with a fatty acid, or a pure non-heat reactive phenolic resin.
The powder blends may optionally include additives such as polyol resins, toluenesulfonamides, or butylated-hydroxy-toluene which enter into the blends as fluxing agents, tending to decrease the melt viscosity of the thermoplastic blend. I
The preferred polyamide resins are produced by the reaction of high molecular weight polyene fatty acids and their esters with an amine. By reacting ammonia, a primary or secondary amine, a hydroxyamine or an alkanolamine, with a high molecular weight carboxylic acid or an ester thereof, either saturated or unsaturated, said acid or ester being obtainable by polymerizing at elevated temperature said polyene fatty acid or esters thereof, and in the case of the esters, converting the polymers to the corresponding acid if desired, there are produced the preferred polyamides. Examples of polyene fatty acids in esterified form are 9,1land/or 9,12-octadecadienoic acid (obtainable from soybean oil and dehydrated castor oil), linoleic acid, alpha and beta-eleostearic acid (obtainable from tung oil). The preferred esters are those derived from methanol, ethanol, and propanol. Primary or secondary amines may be used such as, for example, methylamine, ethylamine, propylamine, ethylenediamine, tetraamethylenediamine, pentamethylenediamine, piperazine, and diethylenetriamine. The class of thermoplastic, polyamide resins is disclosed in U. S. Pat. No. 2,379,413 and sold by the General Mills Company under the trademarks Versamide and Omamid. Other suitable polyamide resins are also available from the Krumbhaar Resin Division of Lawter Chemicals, Inc., under the trademark Polymid.
The second thermoplastic constituent in the electroscopic powder is extremely frangible but it is sharp melting. A suitable frangible constituent may be a rosin-modified phenolic resin, such as those prepared by modifying a phenol formaldehyde resin with the reaction product of maleic anhydride and rosin or a polyhydric alcohol such as glycerol or pentaerythrytol. Such rosin-modified phenolic resins are sold under the trademark Amberol" by Rohm & Hass Company. Diphenolic resin materials esterified with a soya fatty acid and certain thermoplastic phenolformaldehyde resins exhibit satisfactory frangible properties. The esterified diphenolics are available from the Johnson Wax Company Chemical Division of Racine, Wisconsin, and the thermoplastic phenol-formaldehyde resins are available from the Krumbhaar Resin Division of Lawter Chemicals, Inc., and from Nelio Chemicals, Inc., Jacksonville, Florida, as their VBR-800 series resins.
The blend of infrangible and frangible resins with coloring materials forming the electroscopic powder should be highly infrangible and should have a fracturing value of at least 400 grams-centimeters when measured on a wafer of resin 3.75 cm. in diameter and 0.5 cm. in thickness at 100F. by the falling ball method. In this method, as adapted from American Institute of Mining and Metallurgical Engineers, Vol. 87, p. 35, 1930, the resin wafer is subjected to impact by a falling ball and the energy (measured in gram-centimeters) required to just fracture the wafer is measured. The infrangible resin component of the resin blend should preferably have a fracturing value of at least 1000 gram-centimeters in the foregoing test while the frangible resin component may have low fracturing values in the range of 100-200 gram-centimeters.
The resin blend forming the electroscopic powder should not soften or become tacky at temperatures below 130F. The softening properties of resins can be measured with a penetrometer by the procedure of A.S.T.M. Standard No. D5-61. By this procedure, it has been found that resin blends which permit a maximum penetration not greater than 1.0 millimeter at 130F. with a standard needle (No. 4103) in a standard Lab- Line" penetrometer (No. 4100) at a force of 100 grams for 5 seconds resist softening and do not clump or agglomerate during use as electroscopic powder.
The action of the fluxing agent, as an optional component, is believed to lower the melting point of the blend without broadening the melting point range. Successful fluxing agents are provided by the group of polyhydric alcohols sold by the Shell Chemical Company under the trademark "Polyol X-450 of the general formula i al-I5 n FORMULATION NO. 1
(Major percentage of tough, infrangible resin) Polyamide Resin 5090% Frangible resin component (phenollic maleic anhydridepolyhydric alcohol resin) 5-40% Polyols OI0% Nubian resin black l-5% Carbon black pigment (Neo-spectra, Mark III) l-5% FORMULATION NO. 2
(Minor percentage of tough, infrangible resin) Polyamide Resin 9-50% Frangible resin component (Pure phenolics Krumbhaar K-254) 50-90% Polyols O-10% Nubian resin black l-6% Carbon black pigment (Neo-spectra, Mark III) l-2% The following examples are given to illustrate preferred embodiments and process for producing electroscopic powders embodying this invention. It will be understood that this invention is not limited to these examples.
In these examples, all percentages are given on a weight basis.
EXAMPLE 1 Electroscopic powder formulation is:
Synthetic, polyamide, thermoplastic resin (Versamide 930) 33% Polyol (Shell X-450) 9.9% Maleic anhydride-polyhydric alcohol rosin-modified resin (Amberol 800, Rohm & Haas Company) 49.5% Nubian resin black dye 6.6% Carbon black pigment (Neo-spectra, Mark II) l.0%
The quantity of polyamide resin called for is heated in a suitable vessel equipped with a conventional impeller type mixer until the resin is just molten so that it can be stirred. To the molten polyamide resin is added the Polyol while the mass is being agitated. Agitation continues during the addition of the maleic anhydridepolyhydric alcohol rosin-modified resin. After the maleic anhydride-polyhydric alochol resin is completely melted, the quantityof black dye is added to the batch followed by the addition of the carbon black.
After the batch has been thoroughly mixed, it is removed from the mixing vessel, cooled, crushed and pulverized to an average particle size ranging from 4 to 10 microns. Understandably there will be particle sizes ranging from under one micron to 50 microns and larger. As a final step, the electroscopic powder is passed through a 200 mesh screen so that the largest particle size possible in such an electroscopic powder would be under 75 microns.
The softening point of the electroscopic powder was measured by placing a quantity of the electroscopic powders in a constant temperature oven for 12 hours. A series of oven tests, at different temperature levels, revealed that powder produced in Example I remained in particulate form, and did not clump or agglomerate until tested at a 155F. level. The melt point of the electroscopic powder was in the range of 2l5-220F. measured in accordance with A.S.T.M. Method No. E28- 5ST.
The electroscopic powder was combined with iron particles in a ratio of one part powder to 15 parts iron, making a developer mix suitable for developing electrostatic images. The developer mix was charged into the developer unit of a photoelectrostatic copier. More than 50,000 copies were developed with this developer mix requiring the periodic addition of fresh electroscopic powder to replace the amount taken out by the making of copies. Otherwise the developer unit did not require servicing such as complete replacement of the charge, or cleaning of the unit to remove clumps or agglomerates.
The image copies were of uniform density indicating complete and thorough mixing between the carrier and powder. A high image density was maintained throughout the run while non-image areas maintained clean and free of spurious toner deposition. A copy is considered to have proper image density if reflectance density measurements, taken by a standard Photovoltmeter, are above 1.0 units.
Similarly, reflectance readings can give a measure of the contrast between the image and non-image areas. The non-image area on a processed copy should not measure more than 0.05 Photovolt units. The copies were clean in the non-image areas giving Photovolt reading less than 0.05 units.
The copies were not gritty indicating that the carrier particles were being retained in the system and not occluding on the powder.
EXAMPLE 2 Ingredients:
Polyamide resin (Versamide 930) 74% Maleic anhydride-polyhydric alcohol rosin-modified resin (Amberol 800) l9% Nubian resin black dye 5.6% Carbon black pigment (Neo-spectru, Mark ll) l.4%
The ingredients were processed in accordance with the steps set forth for Example 1 above. The melting point range and softening point of the above electroscopic powder were 2l3220F. and greater than 140F., respectively. It will be noted that this example incorporates a major percentage of the tough, infrangible polyamide material. Photovolt readings were all above 1.0 units. Such an electroscopic formulation finds particular utility in environments where the copying equipment is used for extended periods of time and where there is a high ambient temperature.
EXAMPLE 3 An electroscopic powder was prepared in accordance with the procedure of Example 1 wherein the electroscopic powder was comprised largely of polyamide material.
Ingredients:
Polyamide resin (Versamide 930) Maleic anhydride-polyhydric alcohol rosin-modified resin (Amberol 800) 7% Nigrosine dye 6% Polyols 8% Carbon black pigment (Nee-spectra, Mark II) 1% The melting point range and the softening point of the granular mass were 217-222F. and greater than F., respectively. The formulation of Example 3 is suitable for use under high temperature conditions. The inclusion of a fluxing agent tends to lower the melt point slightly and give a more uniform image.
EXAMPLE 4 Ingredients:
Polyamide resin (Versamide 930) 33% Polyol (Shell X-450) fluxing agent 9.9% Phenolic Resin (No. K-254 Krumbhaar Chem. Div. of Lawter Chemicals, Inc.) 49.5% Nubian resin black (National Aniline) 6.6% Carbon black pigment (Nee-spectra, Mark II) The above formula has substituted for the maleic anhydride rosin-modified resin a phenol-formaldehyde resin which is a highly frangible, sharp melting thermoplastic material. The performance of this formulation in respect of print quality and resistance to developer mix deterioration was fully equivalent to that observed in Example 1. The melting point range and softening point of the above example were 21 5-220F. and greater than l40F., respectively.
EXAMPLE 5 EXAMPLE 6 The electroscopic powder prepared in this example conformed to the formula set forth in Example 1 above with the exception that a mixture of orthoand para-N- ethyl-toluene-sulfonamides (Santicizer 8, Monsanto Chemical Company) was substituted as a fluxing agent for the polyol (Shell X450). The copy quality obtained was fully equivalent to the copy quality obtained from the formulation of Example 1.
EXAMPLE 7 This example differs from Example 1 chiefly in the use of lesser percentages of polyamide resin blended with the highly frangible thermoplastic material. It has been found that the addition of polyamide in amounts less than 9 percent by weight in the electrostatic powder formula has little or no effect on improving its resistance to the grinding and milling action present in the developer apparatus.
Polyamide resin (Versamide 930) 9% Maleic anhydride-polyhydric alcohol rosin-modified resin (Amberol 800) 83.2% Nubian resin black 6% Carbon black (Nee-spectra, Mark II) 1% The above composition had a melting point range and softening point of 220-228F. and above 155F., respectively. Electroscopic powders formulated with -6 percent polyamide deteriorated after 3,000-5,000 electrostatic prints. Improvements begin to show when the level of 9 percent, and above, of the polyamide thermoplastic synthetic resin is included in the formula.
All of the foregoing examples when used in the magnetic brush developer of the type described in U. S. Pat. No. 3,003,462 gave consistently dense uniform images. The first copy from a batch of developer mix, and the later copies made after 100 hours of continual use, produced prints having a print density greater than 1.0 Photovolt readings. Reflectance in the non-image area on the developed copy of photoelectrostatic paper was less than 0.05 Photovolt units.
With the developer mix of this invention, the formation of clouds of developer powder or throwout, in the vicinity of the developer mix, is greatly minimized, if not completely prevented. Hence, the areas where such machines are located are kept substantially clean.
A further advantage of the electroscopic powder of this invention is that it does not agglomerate or cake during storage, and therefore remains uniform, ready for use. It is not uncommon for materials in shipment to be exposed to a wide variety of climatic conditions, including extremely high temperatures, which often cause the powder to actually cake into a solid mass in the shipping container. The material of this invention has been found to retain its free-flowing granular consistency, making it ready for use immediately by the operator.
The discussion'of the electroscopic powder has been limited to the technique of positive printing wherein the triboelectric relationship of the electroscopic powder to the iron carrier particles is such that the particles acquire the necessary positive charge so that they will adhere to the negatively charged electrostatic image on the photoconductive member. The advantages provided by the electroscopic powders of this invention may be applied with equal success to the technique of reversal printing as described in co-pendingapplication Ser. No. 221,888 and assigned to the same assignee.
The present invention has been described in great detail, having presented the best mode of formulating the electroscopic powders. Other useful materials and formulations will occur to one skilled in the art over the particular embodiments described herein which are exemplary and not intended to limit the invention, but are intended to cover the invention broadly within the spirit and scope of the appended claims.
What is claimed is:
1. A developer mix for use in electrostatic printing to develop latent images including charged and uncharged areas of an image-bearing sheet, said developer mix comprising the combination of a. separate granular triboelectrically chargeable carrier particles, and
b. a developer powder comprising 1. a coloring agent selected from the group consisting of dyes and pigments, and
2. a resin blend having a triboelectric relationship of opposite polarity with respect to said carrier granules and having a sharp melting point within the range of about C. to about 165 C., said resin blend being formed by mixing the resin components in their molten state and being composed of i. an infrangible thermoplastic polyamide resin formed by reacting a high molecular weight polyene fatty acid or ester thereof with an amine said polyamide resin having a fracturing value of at least 1000 gram centimeters, and
ii. a highly frangible thermoplastic resin having a fracturing value not greater than 200 gram centimeters, said fracturing values being measured by the falling ball method on a wafer of resin maintained at F. and 3.75 centimeters in diameter and 0.5 centimeters in thickness, whereby developed images of substantially improved density can be formed over extended operating periods.
2. A developer mix for use in electrostatic printing to develop latent images including charged and uncharged areas of an image-bearing sheet, said developer mix comprising the combination of a. separate granular magnetically attractable carrier particles, and
b. a developer powder comprising 1. a coloring agent selected from the group consisting of dyes and pigments, and
2. a resin blend having a triboelectric relationship of opposite polarity with respect to said magnetically attractable granules and having a sharp melting point within the range of about 70C. to about C., said resin blend being formed by mixing the resin components in their molten state and being composed of I i. a major portion of an infrangible thermoplastic polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine, and
ii. a minor portion of a highly frangible thermoplastic resin having a fracturing value not greater than 200 gram centimeters, the frangibility of the resins being measured by the falling ball method on a wafer of resin maintained at 100 F. and 3.75 centimeters in diameter and 0.5 centimeters in thickness, whereby developed images of substantially improved density can be formed over extended operating periods.
3. A developer mix as defined by claim 2 wherein the frangible resin is a maleic anhydride rosin-modified resin.
4. An electroscopic powder suitable for developing electrostatic charge images, said powder consisting essentially of frangible and infrangible thermoplastic resins combined when in their molten state to form a miscible mixture, said mixture having physical properties which are distinct from either'of the components comprising said mixture, and having a melting range not greater than 8 F., a softening point not less than 130 F. and a melting point below the char point of paper to which it is applied, said frangible resin constituting 10 to 91 percent by weight of the electroscopic powder and having a fracturing value not greater than 200 grams centimeters, and said infrangible resin being a polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine and constituting to 90 percent by weight of the electroscopic powder and having a fracturing value of at least 1000 gram centimeters, the fracturing value of the resins being measured at 100 F. by the falling ball method on a wafer of resin 3.75 centimeters in diameter and 0.5 centimeters in thickness.
5. The electroscopic powder of claim 4 wherein said powder has a melting point in the range of from 215 to 235 F.
6. The electroscopic powder of claim 4 wherein said powder is comprised of from to 50 percent by weight of said polyamide resin and 50 to 90 percent of a maleicanhydride rosin-modified resin.
7. The electroscopic powder of claim 4 wherein said powder is comprised of from 30 to 40 percent polyamide and 40 to 50 percent maleic anhydride rosinmodified resin and from 1 to 10 percent polyhydric alcohol fluxing agents.
8. The electroscopic powder of claim 4 wherein said powder is comprised of from 50 to 90 percent of said thermoplastic infrangible polyamide resin and from 5 to 40 percent of a frangible thermoplastic resin component selected from the group consisting of maleic anhydride rosin-modified resin, esterified diphenolic resin, and phenol-formaldehyde resins.
9. The electroscopic powder of claim 4 wherein said powder has a particle size range of from 1 micron to 74 microns with an average particle size of from 4 microns to 10 microns.
10. A developer mix for use with magnetic brushtype developing apparatus for rendering latent electrostatic charge images visible on electrostatic recording members by applying thereto an electroscopic powder, and subsequently fixing the adhered powder thereto, said developer mix comprising a granular electroscopic powder of colored thermoplastic particles mixed with larger magnetically attractable carrier particles each having a charge of opposite polarity, said thermoplastic powder having as one component a polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine heat blended with a second frangible resin component to form a composite electroscopic powder having a fracturing value of at least 400 gram centimeters and said polyamide resin having a fracturing value of at least 1000 gram centimeters.
11. The developer mix as claimed in claim 10 wherein said polyamide resin is present in an amount of from 50 to percent by weight of said powder. 12. A developer mix as cliamed in claim 10 wherein the second component is maleic-anhydridepolyhydricalcohol rosin-modified resin in an amount of from 9 to 50 percent by weight of the electroscopic powder.
13. The developer mix as claimed in claim 11 wherein the polyamide resin is a reaction product of polymerized linoleic acid and ethylenediamine.
14. The developer mix as claimed in claim 10 wherein the electroscopic powder has an average particle size in the range of from 4 microns to 10 microns.
15. An improved electrostatic developer mix including carrier particles and colored toner particles, wherein the improvement comprises said toner particles being a hot melt blend of an infrangible thermoplastic resin and a frangible thermoplastic resin wherein physical properties of the resulting blend are distinct from the properties of either of the separate components, said infrangible resin material being a polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine said polyamide resin having a fracturing value of at least 1000 gram centimeters and said frangible material having a fracturing value less than 200 gram centimeters and the fracturing of the blend being at least 400 gram centimeters.
v UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,754,538 Dated October 9 1973 Inventoflxi Loren E. Shelffo It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column 3, Line 50, "50 should read "5 Column 7, Line 39, "maintained" should read "remained".
Column 8, Line 61, the numeral "19" after the period is not required.
Column 11, Line 30, after the word "percent" the words "by weight" should be inserted.
Signed and sealed this 2nd day of July 19%.
(SEAL) Attest:
EDWARD M.FLETCHER,JR. Attesting Officer 0. MARSHALL DANN, Commissioner of Patents FORM PC4050 (10-69) uscoMM-Dc 60376P69 UTS. GOVERNMENT PRINTING OFFICE: 1989 O366'335
Claims (16)
- 2. a resin blend having a triboelectric relationship of opposite polarity with respect to said carrier granules and having a sharp melting point within the range of about 70* C. to about 165* C., said resin blend being formed by mixing the resin components in their molten state and being composed of i. an infrangible thermoplastic polyamide resin formed by reacting a high molecular weight polyene fatty acid or ester thereof with an amine said polyamide resin having a fracturing value of at least 1000 gram centimeters, and ii. a highly frangible thermoplastic resin having a fracturing value not greater than 200 gram centimeters, said fracturing values being measured by the falling ball method on a wafer of resin maintained at 100* F. and 3.75 centimeters in diameter and 0.5 centimeters in thickness, whereby developed images of substantially improved density can be formed over extended operating periods.
- 2. A developer mix for use in electrostatic printing to develop latent images including charged and uncharged areas of an image-bearing sheet, said developer mix comprising the combination of a. separate granular magnetically attractable carrier particles, and b. a developer powder comprising
- 2. a resin blend having a triboelectric relationship of opposite polarity with respect to said magnetically attractable granules and having a sharp melting point within the range of about 70*C. to about 165*C., said resin blend being formed by mixing the resin components in their molten state and being composed of i. a major portion of an infrangible thermoplastic polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine, and ii. a minor portion of a highly frangible thermo-plastic resin having a fracturing value not greater than 200 gram centimeters, the frangibility of the resins being measured by the falling ball method on a wafer of resin maintained at 100* F. and 3.75 centimeters in diameter and 0.5 centimeters in thickness, whereby developed images of substantially improved density can be formed over extended operating periods.
- 3. A developer mix as defined by claim 2 wherein the frangible resin is a maleic anhydride rosin-modified resin.
- 4. An electroscopic powder suitable for developing electrostatic charge images, said powder consisting essentially of frangible and infrangible thermoplastic resins combined when in their molten state to form a miscible mixture, said mixture having physical properties which are distinct from either of the components comprising said mixture, and having a melting range not greater than 8* F., a softening point not less than 130* F. and a melting point below the char point of paper to which it is applied, said frangible resin constituting 10 to 91 percent by weight of the electroscopic powder and having a fracturing value not greater than 200 grams centimeters, and said infrangible resin being a polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine and constituting 5 to 90 percent by weight of the electroscopic powder and having a fracturing value of at least 1000 gram centimeters, the fracturing value of the resins being measured at 100* F. by the falling ball method on a wafer of resin 3.75 centimeters in diameter and 0.5 centimeters in thickness.
- 5. The electroscopic powder of claim 4 wherein said powder has a melting point in the range of from 215* to 235* F.
- 6. The electroscopic powder of claim 4 wherein said powder is comprised of from 10 to 50 percent by weight of said polyamide resin and 50 to 90 percent by weight of a maleic anhydride rosin-modified resin.
- 7. The electroscopic powder of claim 4 wherein said powder is comprised of from 30 to 40 percent polyamide and 40 to 50 percent maleic anhydride rosin-modified resin and from 1 to 10 percent polyhydric alcohol fluxing agents.
- 8. The electroscopic powder of claim 4 wherein said powder is comprised of from 50 to 90 percent of said thermoplastic infrangible polyamide resin and from 5 to 40 percent of a frangible thermoplastic resin component selected from the group consisting of maleic anhydride rosin-modified resin, esterified diphenolic resin, and phenol-formaldehyde resins.
- 9. The electroscopic powder of claim 4 wherein said powder has a particle size range of from 1 micron to 74 microns with an average particle size of from 4 microns to 10 microns.
- 10. A developer mix for use with magnetic brush-type developing apparatus for rendering latent electrostatic charge images visible on electrostatic recording members by applying thereto an electroscopic powder, and subsequently fixing the adhered powder thereto, said developer mix comprising a granular electroscopic powder of colored thermoplastic particles mixed with larger magnetically attractable carrier particles each having a charge of opposite polarity, said thermoplastic powder having as one component a polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine heat blended with a second frangible resin component to form a composite electroscopic powder having a fracturing value of at least 400 gram centimeters and said polyamide resin having a fracturing value of at least 1000 gram centimeters.
- 11. The developer mix as claimed in claim 10 wherein said polyamide resin is present in an amount of from 50 to 90 percent by weight of said powder.
- 12. A developer mix as claimed in claim 10 wherein the second component is maleic-anhydride-polyhydricalcohol rosin-modified resin in an amount of from 9 to 50 percent by weight of the electroscopic powder.
- 13. The developer mix as claimed in claim 11 wherein the polyamide resin is a reaction product of polymerized linoleic acid and ethylenediamine.
- 14. The developer mix as claimed in claim 10 wherein the electroscopic powder has an average particle size in the range of from 4 microns to 10 microns.
- 15. An improved electrostatic developer mix including carrier particles and colored toner particles, wherein the improvement comprises said toner particles being a hot melt blend of an infrangible thermoplastic resin and a frangible thermoplastic resin wherein physical properties of the resulting blend are distinct from the properties of either of the separate components, said infrangible resin material being a polyamide resin formed by reacting a high molecular weight polyene fatty acid or esters thereof with an amine said polyamide resin having a fracturing value of at least 1000 gram centimeters and said frangible material having a fracturing value less than 200 gram centimeters and the fracturing of the blend being at least 400 gram centimeters.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35774364A | 1964-04-06 | 1964-04-06 | |
| US69273267A | 1967-12-22 | 1967-12-22 | |
| US12306571A | 1971-03-10 | 1971-03-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3764538A true US3764538A (en) | 1973-10-09 |
Family
ID=27382909
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00123065A Expired - Lifetime US3764538A (en) | 1964-04-06 | 1971-03-10 | Electroscopic printing powder |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US3764538A (en) |
| GB (1) | GB1108791A (en) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3901695A (en) * | 1964-04-06 | 1975-08-26 | Addressograph Multigraph | Electrophotographic process using polyamide containing developer |
| US4267246A (en) * | 1977-05-17 | 1981-05-12 | Mita Industrial Company Limited | Pressure or heated roller electrophoto image fixing uses halogen or nitrile containing polymer dispersed within resin binder as offset prevent toner |
| US4480023A (en) * | 1983-03-25 | 1984-10-30 | Xerox Corporation | Radiant assist pressure fixing process with polyamide toner compositions |
| US4601966A (en) * | 1985-01-02 | 1986-07-22 | Eastman Kodak Company | Dry, electrographic developer compositions containing polyester-amide toner particles |
| US4845006A (en) * | 1982-09-09 | 1989-07-04 | Konishiroku Photo Industry Co., Ltd. | Toner and process for developing electrostatic latent images |
| US4968574A (en) * | 1980-05-13 | 1990-11-06 | Sekisui Chemical Co., Ltd. | Toner for electrophotography |
| US6406738B1 (en) | 1995-05-09 | 2002-06-18 | Phoqus Limited | Powder coating composition for electrostatic coating of pharmaceutical substrates |
| US20020197388A1 (en) * | 1996-11-13 | 2002-12-26 | Phoqus Limited. | Method and apparatus for the coating of substrates for pharmaceutical use |
| US20030113445A1 (en) * | 2000-02-01 | 2003-06-19 | Martin Trevor Ian | Powder material for electrostatic application to a substrate and electrostatic application of the powder material to a substrate |
| US20030138487A1 (en) * | 1995-05-09 | 2003-07-24 | Phoqus Limited | Powder coating composition for electrostatic coating of pharmaceutical substrates |
| US20070028790A1 (en) * | 2003-06-18 | 2007-02-08 | Phoqus Pharmaceuticals Limited | Method and apparatus for the application of powder material to substrates |
| US20070240976A1 (en) * | 2004-03-31 | 2007-10-18 | Phoqus Pharmaceuticals Limited | Method and Apparatus for the Application of Powder Material to Substrates |
| US20080020147A1 (en) * | 2003-12-30 | 2008-01-24 | Phoqus Pharmaceuticals Limited | Method and Apparatus for the Application of Powder Material to Substrates |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH079546B2 (en) * | 1986-11-17 | 1995-02-01 | 日本合成化学工業株式会社 | Binder for toner |
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| US2221776A (en) * | 1938-09-08 | 1940-11-19 | Chester F Carlson | Electron photography |
| US2297691A (en) * | 1939-04-04 | 1942-10-06 | Chester F Carlson | Electrophotography |
| US2705223A (en) * | 1952-03-11 | 1955-03-29 | Gen Mills Inc | Thermosetting resinous compositions from epoxy resins and polyamides derived from polymeric fat acids |
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Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3901695A (en) * | 1964-04-06 | 1975-08-26 | Addressograph Multigraph | Electrophotographic process using polyamide containing developer |
| US4267246A (en) * | 1977-05-17 | 1981-05-12 | Mita Industrial Company Limited | Pressure or heated roller electrophoto image fixing uses halogen or nitrile containing polymer dispersed within resin binder as offset prevent toner |
| US4968574A (en) * | 1980-05-13 | 1990-11-06 | Sekisui Chemical Co., Ltd. | Toner for electrophotography |
| US4845006A (en) * | 1982-09-09 | 1989-07-04 | Konishiroku Photo Industry Co., Ltd. | Toner and process for developing electrostatic latent images |
| US4480023A (en) * | 1983-03-25 | 1984-10-30 | Xerox Corporation | Radiant assist pressure fixing process with polyamide toner compositions |
| US4601966A (en) * | 1985-01-02 | 1986-07-22 | Eastman Kodak Company | Dry, electrographic developer compositions containing polyester-amide toner particles |
| US20060280943A1 (en) * | 1995-05-09 | 2006-12-14 | Phoqus Pharmaceuticals Limited | Powder coating composition for electrostatic coating of pharmaceutical substrates |
| US6406738B1 (en) | 1995-05-09 | 2002-06-18 | Phoqus Limited | Powder coating composition for electrostatic coating of pharmaceutical substrates |
| US7070656B2 (en) | 1995-05-09 | 2006-07-04 | Phoqus Pharmaceuticals Limited | Electrostatic coating |
| US20030138487A1 (en) * | 1995-05-09 | 2003-07-24 | Phoqus Limited | Powder coating composition for electrostatic coating of pharmaceutical substrates |
| US7008668B2 (en) | 1995-05-09 | 2006-03-07 | Phoqus Pharmaceuticals Limited | Powder coating composition for electrostatic coating of pharmaceutical substrates |
| US20040177809A1 (en) * | 1995-05-09 | 2004-09-16 | Phoqus Limited | Electrostatic coating |
| US20050003074A1 (en) * | 1996-11-13 | 2005-01-06 | Phoqus Pharmaceuticals Limited | Method and apparatus for the coating of substrates for pharmaceutical use |
| US6783768B1 (en) * | 1996-11-13 | 2004-08-31 | Phoqus Pharmaceuticals Limited | Method and apparatus for the coating of substrates for pharmaceutical use |
| US20020197388A1 (en) * | 1996-11-13 | 2002-12-26 | Phoqus Limited. | Method and apparatus for the coating of substrates for pharmaceutical use |
| US7153538B2 (en) | 1996-11-13 | 2006-12-26 | Phoqus Pharmaceuticals Limited | Method and apparatus for the coating of substrates for pharmaceutical use |
| US20030113445A1 (en) * | 2000-02-01 | 2003-06-19 | Martin Trevor Ian | Powder material for electrostatic application to a substrate and electrostatic application of the powder material to a substrate |
| US7285303B2 (en) | 2000-02-01 | 2007-10-23 | Phoqus Pharmaceuticals Limited | Powder material for electrostatic application to a substrate and electrostatic application of the powder material to a substrate |
| US20070028790A1 (en) * | 2003-06-18 | 2007-02-08 | Phoqus Pharmaceuticals Limited | Method and apparatus for the application of powder material to substrates |
| US20080020147A1 (en) * | 2003-12-30 | 2008-01-24 | Phoqus Pharmaceuticals Limited | Method and Apparatus for the Application of Powder Material to Substrates |
| US20070240976A1 (en) * | 2004-03-31 | 2007-10-18 | Phoqus Pharmaceuticals Limited | Method and Apparatus for the Application of Powder Material to Substrates |
| US7732020B2 (en) | 2004-03-31 | 2010-06-08 | Glaxo Group Limited | Method and apparatus for the application of powder material to substrates |
| US20100203256A1 (en) * | 2004-03-31 | 2010-08-12 | Glaxo Group Limited | Method and apparatus for the application of powder material to substrates |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1108791A (en) | 1968-04-03 |
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