Patent US4988600A successfully refreshed from Google Patents.
US4988600A
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Particulate electrophotographic toner material
Assignee: Agfa Gevaert NV
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Filing: 1990-03-13
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Granted: 1991-01-29
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Expires: 2010-03-13
Abstract
Abstract Particulate toner material for use in the development of latent electrostatic images, wherein said particulate toner material is capable of acquiring by triboelectric contact electrification a net positive charge and contains thermoplastic resin(s) as binder in combination with a colorant and a colorless compound capable of imparting a positive charge to the particulate toner material in contact electrification, wherein said colorless compound contains at least one piperidine nucleus substituted with an --NH-acyl group, N-substituted ureido or N-substituted thioureido group.
Inventors
- 👤 Piet Kok
- 👤 Luc J. Vanmaele
- 👤 Serge M. Tavernier
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-03 13:20
CPC Classifications
G; G03; G03G; G03G9/00; G03G9/08; G03G9/097; G03G9/09733; G03G9/09758; G03G9/087; G03G9/08742; G03G9/08768; Y; Y10; Y10S; Y10S430/00; Y10S430/001; Y10S430/104
Claims Analysis
Total Claims: 11
Claim 1
Independent Claim
355 words
Particulate toner material for use in the development of latent electrostatic images, wherein said particulate toner material is capable of acquiring by triboelelectric contact electrification a net positive charge and contains thermoplastic resin(s) as binder in combination with a colorant and a colourless compound capable of imparting a positive charge to the particulate toner material in contact electrification, characterized in that said colourless compound corresponds to the following general Formula (A) or is a polymer consisting essentially of repeating units according to general formula (B) or is an amine-salt or quaternary ammonium derivative thereof: ##STR12## wherein: each of R 1 , R 2 , R 3 and R 4 independently of each other, stands for a 1-6C alkyl group, R 5 represents hydrogen or a 1-5C alkyl group, R 6 represents hydrogen, a 1-12C alkyl group, a 3-12 C alkenyl group, or a 7-12C aralkyl group, m is 1 to 4, and R 7 represents where m is 1 an acyl group, a N-substituted carbamoyl group or a N-substituted thiocarbamoyl group, where m is 2 a carbonyl thiocarbonyl or a diacyl group, a N-substituted dicarbamoyl group or a N-substituted dithiocarbamoyl group, where m is 3 a triacyl group, a N-substituted tricarbamoyl group or a N-substituted trithiocarbamoyl group, and where m is 4 a tetraacyl group, a N-substituted tetracarbamoyl group or a N-substituted tetrathiocarbamoyl group, the N-substituents of said carbamoyl and thiocarbamoyl groups being a hydrocarbon group or a heterocyclic group, and R 8 represents hydrogen an alkyl group or an aralkyl group, or R 7 and Rhu 8 together represent the necessary atoms to close a saturated heterocyclic nitrogen containing ring; ##STR13## wherein: each of R 1 , R 2 , R 3 and R 4 , independently of each other, stands for a 1-6C alkyl group, R 5 represents hydrogen or a 1-5C alkyl group, R 6 represents hydrogen, a 1-12 C alkyl group, a 3-12C alkenyl group, or a 7-12C aralkyl group, each of A and B, independently of each other, represents a 2-12C alkylene group, 7-18 aralkylene group, a 5-12 cycloalkylene group or an arylene group, and n is 2 to 200.
Claim 2
Dependent Claim
355 words
Particulate toner material for use in the development of latent electrostatic images, wherein said particulate toner material is capable of acquiring by triboelelectric contact electrification a net positive charge and contains thermoplastic resin(s) as binder in combination with a colorant and a colourless compound capable of imparting a positive charge to the particulate toner material in contact electrification, characterized in that said colourless compound corresponds to the following general Formula (A) or is a polymer consisting essentially of repeating units according to general formula (B) or is an amine-salt or quaternary ammonium derivative thereof: ##STR12## wherein: each of R 1 , R 2 , R 3 and R 4 independently of each other, stands for a 1-6C alkyl group, R 5 represents hydrogen or a 1-5C alkyl group, R 6 represents hydrogen, a 1-12C alkyl group, a 3-12 C alkenyl group, or a 7-12C aralkyl group, m is 1 to 4, and R 7 represents where m is 1 an acyl group, a N-substituted carbamoyl group or a N-substituted thiocarbamoyl group, where m is 2 a carbonyl thiocarbonyl or a diacyl group, a N-substituted dicarbamoyl group or a N-substituted dithiocarbamoyl group, where m is 3 a triacyl group, a N-substituted tricarbamoyl group or a N-substituted trithiocarbamoyl group, and where m is 4 a tetraacyl group, a N-substituted tetracarbamoyl group or a N-substituted tetrathiocarbamoyl group, the N-substituents of said carbamoyl and thiocarbamoyl groups being a hydrocarbon group or a heterocyclic group, and R 8 represents hydrogen an alkyl group or an aralkyl group, or R 7 and Rhu 8 together represent the necessary atoms to close a saturated heterocyclic nitrogen containing ring; ##STR13## wherein: each of R 1 , R 2 , R 3 and R 4 , independently of each other, stands for a 1-6C alkyl group, R 5 represents hydrogen or a 1-5C alkyl group, R 6 represents hydrogen, a 1-12 C alkyl group, a 3-12C alkenyl group, or a 7-12C aralkyl group, each of A and B, independently of each other, represents a 2-12C alkylene group, 7-18 aralkylene group, a 5-12 cycloalkylene group or an arylene group, and n is 2 to 200.
Claim 3
Dependent Claim
31 words
Particulate toner material according to claim 1, wherein said colourless compound is used in amount in the range of 0.5 to 5% by weight with respect to the total toner composition.
Claim 4
Dependent Claim
36 words
Particulate toner material according to claim 1, wherein said colourless compound is dissolved or dispersed in a thermoplastic hinder being a homopolymer or copolymer of styrene wherein the styrene content is at least 50 mole %.
Claim 5
Dependent Claim
66 words
Particulate toner material according to claim 3, wherein said copolymer is selected from the group consisting of styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer, styrene-n-butyl acrylate copolymer, styrene-n-octyl acrylate copolymer, styrene-methyl methacrylate copolymer, styrene-ethyl methacrylate copolymer, styrene-n-butyl methacrylate copolymer, styrene-isobutyl methacrylate copolymer, styrene-n-octyl methacrylate copolymer styrene-heptadecyl methacrylate copolymer, copoly(styrene-butadiene), and a copolymer of styrene including up to 25% by weight of monomer units comprising a dialkylamino group.
Claim 6
Dependent Claim
13 words
Particulate toner material according to claim 1, wherein the colorant is carbon black.
Claim 7
Dependent Claim
38 words
Particulate toner material according to claim 1, wherein the colorant is an organic pigment or dye selected from the group consisting of phthalocyanine dyes, quinacridone dyes, triaryl methane dyes, sulphur dyes, acridine dyes, azo dyes and fluoresceine dyes.
Claim 8
Dependent Claim
17 words
Particulate toner material according to claim 1, wherein the toner particles incorporate a magnetic or magnetizable material.
Claim 9
Dependent Claim
31 words
Particulate toner material according to claim 1, wherein said material is present in admixture with carrier particles suited for use in cascade-, or magnetic brush development of latent electrostatic charge images.
Claim 10
Dependent Claim
37 words
Particulate toner material according to claim 8, wherein said carrier particles are at least 3 times larger in size than the toner particles and have an average grain size in the range of 50 to 1000 microns.
Claim 11
Dependent Claim
22 words
Particulate toner material according to claim 8, wherein the carrier particles are made of iron or steel provided with an oxide skin.
References Cited (Backward Citations)
US4812379A
Cited
US4927792A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1994-01-28 | 1994-07-30 | 1995-01-29 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1998-01-28 | 1998-07-30 | 1999-01-29 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2002-01-28 | 2002-07-30 | 2003-01-29 | $7700.00 | Window Closed / Lapsed |