SU485608A3 - Электростатографический материал - Google Patents

Электростатографический материал

Info

Publication number: SU485608A3
Authority: SU; USSR - Soviet Union
Prior art keywords: resin; toner; acid; styrene; pigment
Prior art date: 1971-11-11

Application number

SU1847754A

Other languages

English (en)

Russian (ru)

Inventor

Е.Солодар Воррен

Original Assignee

Ксерокс Корпорейшн (Фирма)

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1971-11-11

Filing date

1972-11-10

Publication date

1975-09-25

1972-11-10 Application filed by Ксерокс Корпорейшн (Фирма) filed Critical Ксерокс Корпорейшн (Фирма)

1975-09-25 Application granted granted Critical

1975-09-25 Publication of SU485608A3 publication Critical patent/SU485608A3/ru

Links

239000000463 material Substances 0.000 title claims description 12
229920005989 resin Polymers 0.000 claims description 21
239000011347 resin Substances 0.000 claims description 21
239000002253 acid Substances 0.000 claims description 15
238000000034 method Methods 0.000 claims description 12
239000002245 particle Substances 0.000 claims description 7
-1 that is Substances 0.000 claims description 7
229910052799 carbon Inorganic materials 0.000 claims description 5
229920001577 copolymer Polymers 0.000 claims description 5
239000000049 pigment Substances 0.000 claims description 5
DFYKHEXCUQCPEB-UHFFFAOYSA-N butyl 2-methylprop-2-enoate;styrene Chemical compound C=CC1=CC=CC=C1.CCCCOC(=O)C(C)=C DFYKHEXCUQCPEB-UHFFFAOYSA-N 0.000 claims description 2
229920005990 polystyrene resin Polymers 0.000 claims description 2
239000007787 solid Substances 0.000 claims description 2
UEOIJDKPKBKAGX-UHFFFAOYSA-N 2h-selenopyran Chemical compound C1[Se]C=CC=C1 UEOIJDKPKBKAGX-UHFFFAOYSA-N 0.000 claims 1
230000000712 assembly Effects 0.000 claims 1
238000000429 assembly Methods 0.000 claims 1
150000001768 cations Chemical class 0.000 claims 1
238000010276 construction Methods 0.000 claims 1
239000007921 spray Substances 0.000 claims 1
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 14
125000004432 carbon atom Chemical group C* 0.000 description 13
239000000203 mixture Substances 0.000 description 12
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
238000002844 melting Methods 0.000 description 7
230000008018 melting Effects 0.000 description 7
239000001294 propane Substances 0.000 description 6
239000000243 solution Substances 0.000 description 5
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
229920002554 vinyl polymer Polymers 0.000 description 5
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
150000003254 radicals Chemical class 0.000 description 4
239000001043 yellow dye Substances 0.000 description 4
125000002947 alkylene group Chemical group 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
241000196324 Embryophyta Species 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
229920006026 co-polymeric resin Polymers 0.000 description 2
239000000975 dye Substances 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
239000011147 inorganic material Substances 0.000 description 2
UKWHYYKOEPRTIC-UHFFFAOYSA-N mercury(ii) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000000178 monomer Substances 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
239000004814 polyurethane Substances 0.000 description 2
229920002635 polyurethane Polymers 0.000 description 2
239000012260 resinous material Substances 0.000 description 2
VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
238000005507 spraying Methods 0.000 description 2
PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 2
239000001052 yellow pigment Substances 0.000 description 2
NJVOHKFLBKQLIZ-UHFFFAOYSA-N (2-ethenylphenyl) prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1C=C NJVOHKFLBKQLIZ-UHFFFAOYSA-N 0.000 description 1
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
MNHXWZUNMOPQEX-UHFFFAOYSA-N 2,3-diphenyl-1,3-dihydropyrazole Chemical compound N1C=CC(C=2C=CC=CC=2)N1C1=CC=CC=C1 MNHXWZUNMOPQEX-UHFFFAOYSA-N 0.000 description 1
MZNSQRLUUXWLSB-UHFFFAOYSA-N 2-ethenyl-1h-pyrrole Chemical compound C=CC1=CC=CN1 MZNSQRLUUXWLSB-UHFFFAOYSA-N 0.000 description 1
UJWHLERCFNIFNJ-UHFFFAOYSA-N 4-(ethylamino)phenol Chemical compound CCNC1=CC=C(O)C=C1 UJWHLERCFNIFNJ-UHFFFAOYSA-N 0.000 description 1
RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
101150004109 CYB5R3 gene Proteins 0.000 description 1
101100257033 Caenorhabditis elegans hipr-1 gene Proteins 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
101000708620 Homo sapiens Spermine oxidase Proteins 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
241000600169 Maro Species 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
101100006982 Mus musculus Ppcdc gene Proteins 0.000 description 1
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
206010028980 Neoplasm Diseases 0.000 description 1
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241000282941 Rangifer tarandus Species 0.000 description 1
BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
102100032800 Spermine oxidase Human genes 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
102100030441 Ubiquitin-conjugating enzyme E2 Z Human genes 0.000 description 1
101710192875 Ubiquitin-conjugating enzyme E2 Z Proteins 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000012670 alkaline solution Substances 0.000 description 1
HUMHYXGDUOGHTG-HEZXSMHISA-N alpha-D-GalpNAc-(1->3)-[alpha-L-Fucp-(1->2)]-D-Galp Chemical compound O[C@H]1[C@H](O)[C@H](O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](O[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](O)[C@@H](CO)OC1O HUMHYXGDUOGHTG-HEZXSMHISA-N 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000001273 butane Substances 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
201000011510 cancer Diseases 0.000 description 1
229910002091 carbon monoxide Inorganic materials 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000003086 colorant Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
150000005676 cyclic carbonates Chemical class 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003792 electrolyte Substances 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
150000002085 enols Chemical class 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000000605 extraction Methods 0.000 description 1
210000004709 eyebrow Anatomy 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
239000010436 fluorite Substances 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
210000001035 gastrointestinal tract Anatomy 0.000 description 1
210000003128 head Anatomy 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
238000003384 imaging method Methods 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
238000009413 insulation Methods 0.000 description 1
CVMIVKAWUQZOBP-UHFFFAOYSA-L manganic acid Chemical compound O[Mn](O)(=O)=O CVMIVKAWUQZOBP-UHFFFAOYSA-L 0.000 description 1
229940101209 mercuric oxide Drugs 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
239000011707 mineral Substances 0.000 description 1
150000005673 monoalkenes Chemical class 0.000 description 1
230000035772 mutation Effects 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 1
UMRZSTCPUPJPOJ-KNVOCYPGSA-N norbornane Chemical compound C1C[C@H]2CC[C@@H]1C2 UMRZSTCPUPJPOJ-KNVOCYPGSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
239000011368 organic material Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000003380 propellant Substances 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
210000001187 pylorus Anatomy 0.000 description 1
230000029058 respiratory gaseous exchange Effects 0.000 description 1
229910052711 selenium Inorganic materials 0.000 description 1
239000011669 selenium Substances 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
239000004317 sodium nitrate Substances 0.000 description 1
235000010344 sodium nitrate Nutrition 0.000 description 1
239000010959 steel Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229940110575 tempra Drugs 0.000 description 1
238000001757 thermogravimetry curve Methods 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
230000003612 virological effect Effects 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
238000004383 yellowing Methods 0.000 description 1
239000011787 zinc oxide Substances 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
- G03G9/09—Colouring agents for toner particles
- G03G9/0906—Organic dyes
- G03G9/091—Azo dyes

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Developing Agents For Electrophotography (AREA)

SU1847754A 1971-11-11 1972-11-10 Электростатографический материал SU485608A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US19794371A	1971-11-11	1971-11-11

Publications (1)

Publication Number	Publication Date
SU485608A3 true SU485608A3 (ru)	1975-09-25

Family

ID=22731372

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU1847754A SU485608A3 (ru)	1971-11-11	1972-11-10	Электростатографический материал

Country Status (18)

Country	Link
AR (1)	AR196210A1 (2)
AT (1)	AT321108B (2)
AU (1)	AU471593B2 (2)
BE (1)	BE791194A (2)
BR (1)	BR7207961D0 (2)
CA (1)	CA986767A (2)
CH (1)	CH578195A5 (2)
CS (1)	CS164219B2 (2)
DD (1)	DD103067A5 (2)
DE (1)	DE2253113A1 (2)
FR (1)	FR2187140A5 (2)
GB (1)	GB1398025A (2)
IL (1)	IL40733A (2)
IT (1)	IT1030527B (2)
NL (1)	NL7215214A (2)
SE (1)	SE383051B (2)
SU (1)	SU485608A3 (2)
ZA (1)	ZA727954B (2)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4035310A (en) *	1975-07-28	1977-07-12	Xerox Corporation	Yellow developer
JPS6188153U (2) *	1984-11-13	1986-06-09
DE19717828A1 (de) *	1997-04-26	1998-10-29	Arnold Prof Dr Wartenberg	Verfahren zur Herstellung von Pigmenten aus Textilfarbstoffen und partikulierter Cellulose und Verwendung dieser Pigmente zur Herstellung von Farben, vorzugsweise von Künstlerfarben

0
- BE BE791194D patent/BE791194A/xx unknown
1972
- 1972-10-12 CA CA153,741A patent/CA986767A/en not_active Expired
- 1972-10-30 DE DE2253113A patent/DE2253113A1/de active Pending
- 1972-11-03 IL IL40733A patent/IL40733A/en unknown
- 1972-11-06 CS CS7477A patent/CS164219B2/cs unknown
- 1972-11-07 SE SE7214376A patent/SE383051B/xx unknown
- 1972-11-07 CH CH1620872A patent/CH578195A5/xx not_active IP Right Cessation
- 1972-11-09 GB GB5180472A patent/GB1398025A/en not_active Expired
- 1972-11-09 DD DD166851A patent/DD103067A5/xx unknown
- 1972-11-09 IT IT7231473A patent/IT1030527B/it active
- 1972-11-09 AT AT955072A patent/AT321108B/de not_active IP Right Cessation
- 1972-11-10 AU AU48758/72A patent/AU471593B2/en not_active Expired
- 1972-11-10 ZA ZA727954A patent/ZA727954B/xx unknown
- 1972-11-10 NL NL7215214A patent/NL7215214A/xx unknown
- 1972-11-10 SU SU1847754A patent/SU485608A3/ru active
- 1972-11-10 FR FR7240056A patent/FR2187140A5/fr not_active Expired
- 1972-11-13 AR AR245103A patent/AR196210A1/es active
- 1972-11-13 BR BR7961/72A patent/BR7207961D0/pt unknown

Also Published As

Publication number	Publication date
CA986767A (en)	1976-04-06
CH578195A5 (2)	1976-07-30
BR7207961D0 (pt)	1973-09-27
GB1398025A (en)	1975-06-18
IL40733A (en)	1976-06-30
BE791194A (fr)	1973-05-10
FR2187140A5 (2)	1974-01-11
AU4875872A (en)	1974-05-16
AU471593B2 (en)	1976-04-29
DE2253113A1 (de)	1973-05-17
IL40733A0 (en)	1973-01-30
DD103067A5 (2)	1974-01-05
AT321108B (de)	1975-03-10
IT1030527B (it)	1979-04-10
ZA727954B (en)	1973-07-25
NL7215214A (2)	1973-05-15
SE383051B (sv)	1976-02-23
CS164219B2 (2)	1975-11-07
AR196210A1 (es)	1973-12-10

Publication	Publication Date	Title
Colby et al.	1990	Two-parameter scaling for polymers in θ solvents
TW407149B (en)	2000-10-01	Polymerizable diketooyrrolopyrroles and polymers prepared therewith
US4973539A (en)	1990-11-27	Toner and developer compositions with crosslinked liquid crystalline resins
DE3604827A1 (de)	1987-08-20	Elektrophotographische toner
US2807910A (en)	1957-10-01	Soil conditioning with polyquaternary ammonium compounds
SU485608A3 (ru)	1975-09-25	Электростатографический материал
US4464452A (en)	1984-08-07	Developer compositions containing diaryl sulfonimides
EP0570908A1 (en)	1993-11-24	Electrophotographic photosensitive member, and electrophotographic apparatus and device unit employing the same
DE2630784A1 (de)	1977-02-03	Monomere mit elektronenakzeptorgruppen - herstellungsverfahren und verwendung
JPS6155657A (ja)	1986-03-20	静電荷像現像用トナ−
DE112010003905T5 (de)	2012-11-22	Bindemittelharz für Toner
DE69220619T2 (de)	1998-01-15	Ladungskontrollmittel und Toner zur Entwicklung elektrostatischer Bilder
DE69521662T2 (de)	2002-07-11	Calixarene als Ladungsstabilisatoren und Toner
DE2155905A1 (de)	1972-05-31	Verfahren zur Herstellung eines cokri st allinen Pyryliumfarbstoff-Polymerisat-Komplexes
JPH02244161A (ja)	1990-09-28	ロジン改質スチレンアクリル樹脂からなるトナー組成物
SU654195A3 (ru)	1979-03-25	Материал дл про влени электростатографических изображений
CA1272824A (en)	1990-08-14	Thermoplastic moulding compositions with flame- resistant properties
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