CH510901A - Procédé pour la formation par électrophorèse d'une image - Google Patents

Procédé pour la formation par électrophorèse d'une image

Info

Publication number: CH510901A
Authority: CH; Switzerland
Prior art keywords: particles; photosensitive; electrodes; phenyl; image
Prior art date: 1964-07-23

Application number

CH1874566A

Other languages

English (en)

French (fr)

Inventor

Yeh Shu-Hsiung

Original Assignee

Xerox Corp

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.)

1964-07-23

Filing date

1966-12-29

Publication date

1971-07-31

1966-12-29 Application filed by Xerox Corp filed Critical Xerox Corp

1971-07-31 Publication of CH510901A publication Critical patent/CH510901A/fr

Links

238000000034 method Methods 0.000 title claims description 16
239000002245 particle Substances 0.000 claims description 50
239000000463 material Substances 0.000 claims description 26
230000000903 blocking effect Effects 0.000 claims description 10
239000000725 suspension Substances 0.000 claims description 8
229920005989 resin Polymers 0.000 claims description 6
239000011347 resin Substances 0.000 claims description 6
230000015572 biosynthetic process Effects 0.000 claims description 4
230000005684 electric field Effects 0.000 claims description 3
238000001962 electrophoresis Methods 0.000 claims description 3
239000007788 liquid Substances 0.000 claims description 3
239000006104 solid solution Substances 0.000 claims description 3
230000003213 activating effect Effects 0.000 claims description 2
239000011248 coating agent Substances 0.000 claims description 2
238000000576 coating method Methods 0.000 claims description 2
230000005670 electromagnetic radiation Effects 0.000 claims description 2
239000011159 matrix material Substances 0.000 claims description 2
239000011162 core material Substances 0.000 claims 1
239000000975 dye Substances 0.000 description 9
-1 polyethylene Polymers 0.000 description 9
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 8
VHQGURIJMFPBKS-UHFFFAOYSA-N 2,4,7-trinitrofluoren-9-one Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=C2C3=CC=C([N+](=O)[O-])C=C3C(=O)C2=C1 VHQGURIJMFPBKS-UHFFFAOYSA-N 0.000 description 7
239000000203 mixture Substances 0.000 description 7
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 6
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical group N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 6
230000035945 sensitivity Effects 0.000 description 5
239000002904 solvent Substances 0.000 description 5
229910052601 baryte Inorganic materials 0.000 description 4
239000010428 baryte Substances 0.000 description 4
239000012876 carrier material Substances 0.000 description 4
229920001577 copolymer Polymers 0.000 description 4
239000011521 glass Substances 0.000 description 4
238000003384 imaging method Methods 0.000 description 4
239000011787 zinc oxide Substances 0.000 description 4
WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 3
CMSGUKVDXXTJDQ-UHFFFAOYSA-N 4-(2-naphthalen-1-ylethylamino)-4-oxobutanoic acid Chemical compound C1=CC=C2C(CCNC(=O)CCC(=O)O)=CC=CC2=C1 CMSGUKVDXXTJDQ-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
239000000370 acceptor Substances 0.000 description 3
239000002253 acid Substances 0.000 description 3
229910052980 cadmium sulfide Inorganic materials 0.000 description 3
230000009965 odorless effect Effects 0.000 description 3
239000005011 phenolic resin Substances 0.000 description 3
229920000647 polyepoxide Polymers 0.000 description 3
PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 3
229940043267 rhodamine b Drugs 0.000 description 3
239000000243 solution Substances 0.000 description 3
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 2
ASDLSKCKYGVMAI-UHFFFAOYSA-N 9,10-dioxoanthracene-2-carboxylic acid Chemical compound C1=CC=C2C(=O)C3=CC(C(=O)O)=CC=C3C(=O)C2=C1 ASDLSKCKYGVMAI-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
239000004305 biphenyl Substances 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
239000011575 calcium Substances 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
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239000002800 charge carrier Substances 0.000 description 2
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239000003822 epoxy resin Substances 0.000 description 2
PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
229920001568 phenolic resin Polymers 0.000 description 2
239000000049 pigment Substances 0.000 description 2
230000004044 response Effects 0.000 description 2
230000003595 spectral effect Effects 0.000 description 2
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 1
DXBHBZVCASKNBY-UHFFFAOYSA-N 1,2-Benz(a)anthracene Chemical compound C1=CC=C2C3=CC4=CC=CC=C4C=C3C=CC2=C1 DXBHBZVCASKNBY-UHFFFAOYSA-N 0.000 description 1
YNANGXWUZWWFKX-UHFFFAOYSA-N 1,2-bis(4-methoxyphenyl)ethane-1,2-dione Chemical compound C1=CC(OC)=CC=C1C(=O)C(=O)C1=CC=C(OC)C=C1 YNANGXWUZWWFKX-UHFFFAOYSA-N 0.000 description 1
KZPCZVOCQJULBN-UHFFFAOYSA-N 1,3-bis(4-chlorophenyl)imidazolidine Chemical compound C1=CC(Cl)=CC=C1N1CN(C=2C=CC(Cl)=CC=2)CC1 KZPCZVOCQJULBN-UHFFFAOYSA-N 0.000 description 1
WYEYGPJVIZYKNM-UHFFFAOYSA-N 1,3-diphenylimidazolidine Chemical compound C1CN(C=2C=CC=CC=2)CN1C1=CC=CC=C1 WYEYGPJVIZYKNM-UHFFFAOYSA-N 0.000 description 1
YTGSYRVSBPFKMQ-UHFFFAOYSA-N 2,2,2-tribromoacetaldehyde Chemical compound BrC(Br)(Br)C=O YTGSYRVSBPFKMQ-UHFFFAOYSA-N 0.000 description 1
JVTSHOJDBRTPHD-UHFFFAOYSA-N 2,2,2-trifluoroacetaldehyde Chemical compound FC(F)(F)C=O JVTSHOJDBRTPHD-UHFFFAOYSA-N 0.000 description 1
WJCZICXCIDVPOP-UHFFFAOYSA-N 2,3,4,5-tetraphenyl-1,3-dihydropyrazole Chemical compound N1N(C=2C=CC=CC=2)C(C=2C=CC=CC=2)C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 WJCZICXCIDVPOP-UHFFFAOYSA-N 0.000 description 1
IPXSAYARKMFWCP-UHFFFAOYSA-N 2,3,4-triphenyl-1h-pyrrole Chemical compound C=1NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)C=1C1=CC=CC=C1 IPXSAYARKMFWCP-UHFFFAOYSA-N 0.000 description 1
AXSVCKIFQVONHI-UHFFFAOYSA-N 2,3-bis(4-methoxyphenyl)-1-benzofuran-6-ol Chemical compound C1=CC(OC)=CC=C1C1=C(C=2C=CC(OC)=CC=2)C2=CC=C(O)C=C2O1 AXSVCKIFQVONHI-UHFFFAOYSA-N 0.000 description 1
FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 1
QAHMKHHCOXNIHO-UHFFFAOYSA-N 2,4-diphenylquinazoline Chemical compound C1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=CC=C2)C2=N1 QAHMKHHCOXNIHO-UHFFFAOYSA-N 0.000 description 1
LNXVNZRYYHFMEY-UHFFFAOYSA-N 2,5-dichlorocyclohexa-2,5-diene-1,4-dione Chemical compound ClC1=CC(=O)C(Cl)=CC1=O LNXVNZRYYHFMEY-UHFFFAOYSA-N 0.000 description 1
TXWSZJSDZKWQAU-UHFFFAOYSA-N 2,9-dimethyl-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione Chemical compound N1C2=CC=C(C)C=C2C(=O)C2=C1C=C(C(=O)C=1C(=CC=C(C=1)C)N1)C1=C2 TXWSZJSDZKWQAU-UHFFFAOYSA-N 0.000 description 1
AOPZIJQISHFZBN-UHFFFAOYSA-N 2-(4-methoxyphenyl)-1,3-benzothiazole Chemical compound C1=CC(OC)=CC=C1C1=NC2=CC=CC=C2S1 AOPZIJQISHFZBN-UHFFFAOYSA-N 0.000 description 1
KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
XQGDNRFLRLSUFQ-UHFFFAOYSA-N 2H-pyranthren-1-one Chemical class C1=C(C2=C3C4=C56)C=CC3=CC5=C3C=CC=CC3=CC6=CC=C4C=C2C2=C1C(=O)CC=C2 XQGDNRFLRLSUFQ-UHFFFAOYSA-N 0.000 description 1
ZMESCNYFNZEIFB-UHFFFAOYSA-N 3-(4-methoxyphenyl)-5-[2-(4-methoxyphenyl)ethenyl]-2-phenyl-1,3-dihydropyrazole Chemical compound C1=CC(OC)=CC=C1C=CC1=CC(C=2C=CC(OC)=CC=2)N(C=2C=CC=CC=2)N1 ZMESCNYFNZEIFB-UHFFFAOYSA-N 0.000 description 1
YXJBVSMIBWFMCV-UHFFFAOYSA-N 3-(6-amino-1,4-dimethylcyclohexa-2,4-dien-1-yl)-2-phenyl-1-benzofuran-6-ol Chemical compound OC1=CC2=C(C(=C(O2)C2=CC=CC=C2)C2(C(C=C(C=C2)C)N)C)C=C1 YXJBVSMIBWFMCV-UHFFFAOYSA-N 0.000 description 1
GEBZDNUANAGYMF-UHFFFAOYSA-N 3-benzylidenecarbazol-1-amine Chemical compound C1=C2C3=CC=CC=C3N=C2C(N)=CC1=CC1=CC=CC=C1 GEBZDNUANAGYMF-UHFFFAOYSA-N 0.000 description 1
OTLLZASEKLGFMH-UHFFFAOYSA-N 4,5-diphenylimidazol-2-one Chemical compound N=1C(=O)N=C(C=2C=CC=CC=2)C=1C1=CC=CC=C1 OTLLZASEKLGFMH-UHFFFAOYSA-N 0.000 description 1
MLAJDFOBMYBISF-UHFFFAOYSA-N 4,5-diphenylimidazolidin-2-one Chemical compound N1C(=O)NC(C=2C=CC=CC=2)C1C1=CC=CC=C1 MLAJDFOBMYBISF-UHFFFAOYSA-N 0.000 description 1
WEROHEHOBCONLN-UHFFFAOYSA-N 4-(4-phenylquinazolin-2-yl)aniline Chemical compound C1=CC(N)=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=CC=C2)C2=N1 WEROHEHOBCONLN-UHFFFAOYSA-N 0.000 description 1
BLEJLJKBALJKGI-UHFFFAOYSA-N 4-(5,6-diphenyl-1,2,4-triazin-3-yl)aniline Chemical compound C1=CC(N)=CC=C1C(N=C1C=2C=CC=CC=2)=NN=C1C1=CC=CC=C1 BLEJLJKBALJKGI-UHFFFAOYSA-N 0.000 description 1
IAYXCYQZMSGSBL-UHFFFAOYSA-N 4-(7-methoxy-2-phenylquinazolin-4-yl)-n,n-dimethylaniline Chemical compound N=1C2=CC(OC)=CC=C2C(C=2C=CC(=CC=2)N(C)C)=NC=1C1=CC=CC=C1 IAYXCYQZMSGSBL-UHFFFAOYSA-N 0.000 description 1
DAVALMOPPDVYEZ-UHFFFAOYSA-N 4-[[4-(dimethylamino)phenyl]iminomethyl]-3-nitrobenzonitrile Chemical compound C1=CC(N(C)C)=CC=C1N=CC1=CC=C(C#N)C=C1[N+]([O-])=O DAVALMOPPDVYEZ-UHFFFAOYSA-N 0.000 description 1
BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 description 1
VXWYTPFBWXNAJG-UHFFFAOYSA-N 5-(1-methylbenzimidazol-2-yl)-6-methylidenecyclohexa-1,3-diene-1,2-diol Chemical compound CN1C(=NC2=C1C=CC=C2)C2C(C(=C(C=C2)O)O)=C VXWYTPFBWXNAJG-UHFFFAOYSA-N 0.000 description 1
WUMNREMXKHAYJQ-UHFFFAOYSA-N 5-methyl-2,3-diphenyl-1,3-dihydropyrazole Chemical compound N1C(C)=CC(C=2C=CC=CC=2)N1C1=CC=CC=C1 WUMNREMXKHAYJQ-UHFFFAOYSA-N 0.000 description 1
LRSYZHFYNDZXMU-UHFFFAOYSA-N 9h-carbazol-3-amine Chemical compound C1=CC=C2C3=CC(N)=CC=C3NC2=C1 LRSYZHFYNDZXMU-UHFFFAOYSA-N 0.000 description 1
229920003319 Araldite® Polymers 0.000 description 1
UNMYWSMUMWPJLR-UHFFFAOYSA-L Calcium iodide Chemical compound [Ca+2].[I-].[I-] UNMYWSMUMWPJLR-UHFFFAOYSA-L 0.000 description 1
229920000298 Cellophane Polymers 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
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108010010803 Gelatin Proteins 0.000 description 1
240000004343 Indigofera suffruticosa Species 0.000 description 1
235000000177 Indigofera tinctoria Nutrition 0.000 description 1
229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
239000002841 Lewis acid Substances 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
BZORFPDSXLZWJF-UHFFFAOYSA-N N,N-dimethyl-1,4-phenylenediamine Chemical compound CN(C)C1=CC=C(N)C=C1 BZORFPDSXLZWJF-UHFFFAOYSA-N 0.000 description 1
239000000020 Nitrocellulose Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
206010070834 Sensitisation Diseases 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
238000005411 Van der Waals force Methods 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
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239000005083 Zinc sulfide Substances 0.000 description 1
ZQRRBZZVXPVWRB-UHFFFAOYSA-N [S].[Se] Chemical compound [S].[Se] ZQRRBZZVXPVWRB-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
WLDHEUZGFKACJH-UHFFFAOYSA-K amaranth Chemical compound [Na+].[Na+].[Na+].C12=CC=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(O)=C1N=NC1=CC=C(S([O-])(=O)=O)C2=CC=CC=C12 WLDHEUZGFKACJH-UHFFFAOYSA-K 0.000 description 1
150000004056 anthraquinones Chemical class 0.000 description 1
IKIBSPLDJGAHPX-UHFFFAOYSA-N arsenic triiodide Chemical compound I[As](I)I IKIBSPLDJGAHPX-UHFFFAOYSA-N 0.000 description 1
159000000009 barium salts Chemical class 0.000 description 1
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
239000012965 benzophenone Substances 0.000 description 1
229950011260 betanaphthol Drugs 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical class FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
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SRPCPRSDICCCRQ-UHFFFAOYSA-N chembl2004385 Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(N=NC3=C4C=CC=CC4=CC=C3O)=CC=C21 SRPCPRSDICCCRQ-UHFFFAOYSA-N 0.000 description 1
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125000001309 chloro group Chemical group Cl* 0.000 description 1
UZDWIWGMKWZEPE-UHFFFAOYSA-K chromium(iii) bromide Chemical compound [Cr+3].[Br-].[Br-].[Br-] UZDWIWGMKWZEPE-UHFFFAOYSA-K 0.000 description 1
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PLYDMIIYRWUYBP-UHFFFAOYSA-N ethyl 4-[[2-chloro-4-[3-chloro-4-[(3-ethoxycarbonyl-5-oxo-1-phenyl-4h-pyrazol-4-yl)diazenyl]phenyl]phenyl]diazenyl]-5-oxo-1-phenyl-4h-pyrazole-3-carboxylate Chemical compound CCOC(=O)C1=NN(C=2C=CC=CC=2)C(=O)C1N=NC(C(=C1)Cl)=CC=C1C(C=C1Cl)=CC=C1N=NC(C(=N1)C(=O)OCC)C(=O)N1C1=CC=CC=C1 PLYDMIIYRWUYBP-UHFFFAOYSA-N 0.000 description 1
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235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
235000019239 indanthrene blue RS Nutrition 0.000 description 1
UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 1
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150000002500 ions Chemical class 0.000 description 1
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229910000464 lead oxide Inorganic materials 0.000 description 1
229910052981 lead sulfide Inorganic materials 0.000 description 1
229940056932 lead sulfide Drugs 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
OTCKOJUMXQWKQG-UHFFFAOYSA-L magnesium bromide Chemical compound [Mg+2].[Br-].[Br-] OTCKOJUMXQWKQG-UHFFFAOYSA-L 0.000 description 1
229910001623 magnesium bromide Inorganic materials 0.000 description 1
LBAIJNRSTQHDMR-UHFFFAOYSA-N magnesium phthalocyanine Chemical compound [Mg].C12=CC=CC=C2C(N=C2NC(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2N1 LBAIJNRSTQHDMR-UHFFFAOYSA-N 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229910001507 metal halide Inorganic materials 0.000 description 1
150000005309 metal halides Chemical class 0.000 description 1
229910052752 metalloid Inorganic materials 0.000 description 1
150000002738 metalloids Chemical class 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
JFTBTTPUYRGXDG-UHFFFAOYSA-N methyl violet Chemical compound Cl.C1=CC(=NC)C=CC1=C(C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 JFTBTTPUYRGXDG-UHFFFAOYSA-N 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
239000000178 monomer Substances 0.000 description 1
XLGSXVUJWBCURQ-UHFFFAOYSA-N n-(4-bromophenyl)-1-(2-nitrophenyl)methanimine Chemical compound [O-][N+](=O)C1=CC=CC=C1C=NC1=CC=C(Br)C=C1 XLGSXVUJWBCURQ-UHFFFAOYSA-N 0.000 description 1
KOJOUCAVSDKDPR-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)benzamide Chemical compound C=1C=CC=2C(=O)C3=CC=CC=C3C(=O)C=2C=1NC(=O)C1=CC=CC=C1 KOJOUCAVSDKDPR-UHFFFAOYSA-N 0.000 description 1
DWXAPYADWDBIII-UHFFFAOYSA-N n-[[4-(dimethylamino)phenyl]methylideneamino]benzamide Chemical compound C1=CC(N(C)C)=CC=C1C=NNC(=O)C1=CC=CC=C1 DWXAPYADWDBIII-UHFFFAOYSA-N 0.000 description 1
MSHOEHQTHKGVOD-UHFFFAOYSA-N n-[[4-(dimethylamino)phenyl]methylideneamino]pyridine-4-carboxamide Chemical compound C1=CC(N(C)C)=CC=C1C=NNC(=O)C1=CC=NC=C1 MSHOEHQTHKGVOD-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
150000002979 perylenes Chemical class 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
239000013034 phenoxy resin Substances 0.000 description 1
229920006287 phenoxy resin Polymers 0.000 description 1
OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000139 polyethylene terephthalate Polymers 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920001343 polytetrafluoroethylene Polymers 0.000 description 1
239000004810 polytetrafluoroethylene Substances 0.000 description 1
229920002620 polyvinyl fluoride Polymers 0.000 description 1
239000004065 semiconductor Substances 0.000 description 1
230000008313 sensitization Effects 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
235000011150 stannous chloride Nutrition 0.000 description 1
239000001119 stannous chloride Substances 0.000 description 1
YJPVTCSBVRMESK-UHFFFAOYSA-L strontium bromide Chemical compound [Br-].[Br-].[Sr+2] YJPVTCSBVRMESK-UHFFFAOYSA-L 0.000 description 1
229910001625 strontium bromide Inorganic materials 0.000 description 1
229940074155 strontium bromide Drugs 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
QXKXDIKCIPXUPL-UHFFFAOYSA-N sulfanylidenemercury Chemical compound [Hg]=S QXKXDIKCIPXUPL-UHFFFAOYSA-N 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 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
AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 0.000 description 1
150000003673 urethanes Chemical class 0.000 description 1
KOTVVDDZWMCZBT-UHFFFAOYSA-N vat violet 1 Chemical compound C1=CC=C[C]2C(=O)C(C=CC3=C4C=C(C=5C=6C(C([C]7C=CC=CC7=5)=O)=CC=C5C4=6)Cl)=C4C3=C5C=C(Cl)C4=C21 KOTVVDDZWMCZBT-UHFFFAOYSA-N 0.000 description 1
239000001043 yellow dye Substances 0.000 description 1
239000011592 zinc chloride Substances 0.000 description 1
235000005074 zinc chloride Nutrition 0.000 description 1
229910052984 zinc sulfide Inorganic materials 0.000 description 1
DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G17/00—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process
- G03G17/04—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process using photoelectrophoresis
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/14—Transferring a pattern to a second base
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G15/00—Apparatus for electrographic processes using a charge pattern
- G03G15/01—Apparatus for electrographic processes using a charge pattern for producing multicoloured copies

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Electrochemistry (AREA)
Molecular Biology (AREA)
Photoreceptors In Electrophotography (AREA)
Sampling And Sample Adjustment (AREA)
Materials For Photolithography (AREA)

CH1874566A 1964-07-23 1966-12-29 Procédé pour la formation par électrophorèse d'une image CH510901A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US38468064A	1964-07-23	1964-07-23
US518041A US3383993A (en)	1964-07-23	1966-01-03	Photoelectrophoretic imaging apparatus

Publications (1)

Publication Number	Publication Date
CH510901A true CH510901A (fr)	1971-07-31

Family

ID=27010705

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1874566A CH510901A (fr)	1964-07-23	1966-12-29	Procédé pour la formation par électrophorèse d'une image

Country Status (7)

Country	Link
US (1)	US3383993A (de)
AT (1)	AT305765B (de)
CH (1)	CH510901A (de)
DE (1)	DE1522750A1 (de)
FR (1)	FR1507051A (de)
LU (1)	LU52738A1 (de)
NL (1)	NL150926B (de)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3897143A (en) *	1965-05-28	1975-07-29	Xerox Corp	Imaging system
SE336525B (de) *	1966-06-29	1971-07-05	Xerox Corp
US3619054A (en) *	1966-08-09	1971-11-09	Xerox Corp	Oil film imaging apparatus
US3539255A (en) *	1966-09-23	1970-11-10	Xerox Corp	Xerographic recording apparatus
US3546085A (en) *	1967-01-30	1970-12-08	Xerox Corp	Photoelectrophoretic imaging process and suspension
US3535221A (en) *	1967-10-17	1970-10-20	Xerox Corp	Photoelectrophoretic imaging system employing a photoconductor coating for the blocking electrode
US3610748A (en) *	1969-06-25	1971-10-05	Xerox Corp	Photoelectrophoretic imaging system
US3854943A (en) *	1969-07-30	1974-12-17	Xerox Corp	Manifold imaging method and member employing fundamental particles of alpha metal-free phthalocyanine
US3619053A (en) *	1969-09-17	1971-11-09	Xerox Corp	Photoelectrophoretic imaging system
BE756481A (fr) *	1969-09-23	1971-03-22	Xerox Corp	Procede de formation d'image photoelectrophoretique par reflexion
US3881920A (en) *	1969-10-02	1975-05-06	Xerox Corp	Photoelectrophoretic imaging process
USRE28360E (en) *	1969-10-03	1975-03-04		Electrophoretic color display device
US3612758A (en) *	1969-10-03	1971-10-12	Xerox Corp	Color display device
US3690754A (en) *	1969-11-14	1972-09-12	Xerox Corp	Control system for an optical imaging system
US3644035A (en) *	1969-11-14	1972-02-22	Xerox Corp	Flat plate traveling roller imaging system
US3623122A (en) *	1970-06-04	1971-11-23	Horizons Research Inc	Electric recording apparatus employing liquid developer
US3792308A (en) *	1970-06-08	1974-02-12	Matsushita Electric Industrial Co Ltd	Electrophoretic display device of the luminescent type
US3804660A (en) *	1970-08-17	1974-04-16	Commw Of Australia	Dielectric recording on insulator surfaces
US3850630A (en) *	1970-12-01	1974-11-26	Xerox Corp	Xerographic plate containing photoinjection indigold pigments
US3684365A (en) *	1971-07-08	1972-08-15	Varian Associates	Display tube camera system allowing an observer an unobstructed view of the display
CH594921A5 (de) *	1972-10-26	1978-01-31	Gretag Ag
JPS5312187B2 (de) *	1973-03-29	1978-04-27
US3917880A (en) *	1973-06-27	1975-11-04	Xerox Corp	Electrophoretic imaging system
US4175956A (en) *	1978-02-10	1979-11-27	Eastman Kodak Company	Electrophotosensitive materials for migration imaging processes
US4314013A (en) *	1979-04-04	1982-02-02	Xerox Corporation	Particle formation by double encapsulation
US4431721A (en) *	1981-06-29	1984-02-14	Ciba-Geigy Corporation	Use of perylene pigments for photoelectrophoretic imaging
US10254620B1 (en)	2016-03-08	2019-04-09	E Ink Corporation	Encapsulated photoelectrophoretic display
JP6666285B2 (ja) *	2017-03-03	2020-03-13	株式会社東芝	放射線検出器
EP3593340B1 (de)	2017-03-06	2021-11-03	E Ink Corporation	Verfahren zur darstellung von farbbildern
US11404013B2 (en)	2017-05-30	2022-08-02	E Ink Corporation	Electro-optic displays with resistors for discharging remnant charges
WO2018222638A1 (en)	2017-05-30	2018-12-06	E Ink Corporation	Electro-optic displays
EP4343420A3 (de)	2018-05-17	2024-05-01	E Ink Corporation	Verfahren zur herstellung einer piezoelektrophoretischen anzeige
JP7104852B2 (ja)	2018-08-14	2022-07-21	イーインクカリフォルニア，エルエルシー	圧電電気泳動ディスプレイ

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2839400A (en) *	1953-10-30	1958-06-17	Rca Corp	Electrostatic printing
US2758939A (en) *	1953-12-30	1956-08-14	Rca Corp	Electrostatic printing
US2940847A (en) *	1957-07-03	1960-06-14		None i red
BE614376A (de) *	1961-02-27
NL285527A (de) *	1961-11-15

1965
- 1965-07-22 AT AT254770A patent/AT305765B/de not_active IP Right Cessation
1966
- 1966-01-03 US US518041A patent/US3383993A/en not_active Expired - Lifetime
- 1966-12-29 CH CH1874566A patent/CH510901A/fr not_active IP Right Cessation
- 1966-12-30 FR FR89586A patent/FR1507051A/fr not_active Expired
1967
- 1967-01-03 DE DE19671522750 patent/DE1522750A1/de active Pending
- 1967-01-03 LU LU52738D patent/LU52738A1/xx unknown
- 1967-01-03 NL NL676700090A patent/NL150926B/xx unknown

Also Published As

Publication number	Publication date
DE1522750A1 (de)	1969-10-30
NL150926B (nl)	1976-09-15
AT305765B (de)	1973-03-12
NL6700090A (de)	1967-07-04
LU52738A1 (de)	1967-03-14
FR1507051A (fr)	1967-12-22
US3383993A (en)	1968-05-21

Legal Events

Date	Code	Title	Description
1982-08-31	PL	Patent ceased

Publication	Publication Date	Title
CH510901A (fr)	1971-07-31	Procédé pour la formation par électrophorèse d'une image
US3384566A (en)	1968-05-21	Method of photoelectrophoretic imaging
US4415639A (en)	1983-11-15	Multilayered photoresponsive device for electrophotography
US4264695A (en)	1981-04-28	Electrophotographic photosensitive material with electron donors and electron acceptors
DE2938129C2 (de)	1983-07-14	Elektrophotographisches Aufzeichnungsmaterial
JPH02131243A (ja)	1990-05-21	電子写真感光体
US5055367A (en)	1991-10-08	Imaging members with bichromophoric bisazo perinone photoconductive materials
JPS6242498B2 (de)	1987-09-08
JPS6247054A (ja)	1987-02-28	電子写真用感光体
JPS6334464B2 (de)	1988-07-11
US4370398A (en)	1983-01-25	Electrostatic copying process
JP3176797B2 (ja)	2001-06-18	電子写真用感光体
US3616398A (en)	1971-10-26	A photoelectrophoretic imaging composition containing b-carotene
JPS59125735A (ja)	1984-07-20	電子写真用感光体
JPH0342662B2 (de)	1991-06-27
JPH0342660B2 (de)	1991-06-27
JPS62121460A (ja)	1987-06-02	電子写真感光体
US3776721A (en)	1973-12-04	Manifold imaging
US4108656A (en)	1978-08-22	Photoconductive member having a charge generating pigment and 2,4,7-trinitrothioxanthone as charge transport material
JPH0354341B2 (de)	1991-08-19
US3989860A (en)	1976-11-02	Repair technique for photoreceptors
Weigl et al.	1972	Phthalocyanine-binder photoreceptors for xerography
JPS59170846A (ja)	1984-09-27	積層型電子写真感光体
JPS61144657A (ja)	1986-07-02	電子写真感光体
DE3014002A1 (de)	1980-10-16	Photoempfindliches kompositmaterial fuer elektrophotographische zwecke