US3441947A - Thermoplastic recording process - Google Patents
Thermoplastic recording process Download PDFInfo
- Publication number
- US3441947A US3441947A US3441947DA US3441947A US 3441947 A US3441947 A US 3441947A US 3441947D A US3441947D A US 3441947DA US 3441947 A US3441947 A US 3441947A
- Authority
- US
- United States
- Prior art keywords
- layer
- vinyl
- poly
- photoconductive
- copolymer
- 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
Links
- 238000000034 method Methods 0.000 title claims description 36
- 229920001169 thermoplastic Polymers 0.000 title claims description 15
- 239000004416 thermosoftening plastic Substances 0.000 title claims description 15
- 239000010410 layer Substances 0.000 claims description 28
- 239000000463 material Substances 0.000 claims description 23
- 230000005670 electromagnetic radiation Effects 0.000 claims description 9
- 239000013047 polymeric layer Substances 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 7
- 230000003287 optical effect Effects 0.000 claims description 5
- 239000004020 conductor Substances 0.000 claims description 4
- 239000002344 surface layer Substances 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 description 33
- -1 Poly (vinyl acetal Chemical class 0.000 description 29
- 239000007795 chemical reaction product Substances 0.000 description 29
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 29
- 229920002554 vinyl polymer Polymers 0.000 description 24
- 229920000728 polyester Polymers 0.000 description 18
- 239000002253 acid Substances 0.000 description 17
- 238000002844 melting Methods 0.000 description 15
- 230000008018 melting Effects 0.000 description 15
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- 229920000915 polyvinyl chloride Polymers 0.000 description 11
- 239000004800 polyvinyl chloride Substances 0.000 description 11
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 10
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 10
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 10
- 229940117958 vinyl acetate Drugs 0.000 description 10
- 229920001634 Copolyester Polymers 0.000 description 8
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 8
- 229920006163 vinyl copolymer Polymers 0.000 description 8
- 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 7
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 6
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 239000001294 propane Substances 0.000 description 6
- 229920001897 terpolymer Polymers 0.000 description 6
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 5
- 229920000578 graft copolymer Polymers 0.000 description 5
- 230000000306 recurrent effect Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- 235000010290 biphenyl Nutrition 0.000 description 4
- 239000004305 biphenyl Substances 0.000 description 4
- 125000006267 biphenyl group Chemical group 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 125000000623 heterocyclic group Chemical group 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 4
- RNIPJYFZGXJSDD-UHFFFAOYSA-N 2,4,5-triphenyl-1h-imidazole Chemical compound C1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 RNIPJYFZGXJSDD-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 3
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 3
- 229950000688 phenothiazine Drugs 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000001454 recorded image Methods 0.000 description 3
- 239000012815 thermoplastic material Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 2
- YMTYZTXUZLQUSF-UHFFFAOYSA-N 3,3'-Dimethylbisphenol A Chemical compound C1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=CC=2)=C1 YMTYZTXUZLQUSF-UHFFFAOYSA-N 0.000 description 2
- CPHGOBGXZQKCKI-UHFFFAOYSA-N 4,5-diphenyl-1h-imidazole Chemical compound N1C=NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 CPHGOBGXZQKCKI-UHFFFAOYSA-N 0.000 description 2
- PLAZXGNBGZYJSA-UHFFFAOYSA-N 9-ethylcarbazole Chemical compound C1=CC=C2N(CC)C3=CC=CC=C3C2=C1 PLAZXGNBGZYJSA-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- HTVITOHKHWFJKO-UHFFFAOYSA-N Bisphenol B Chemical compound C=1C=C(O)C=CC=1C(C)(CC)C1=CC=C(O)C=C1 HTVITOHKHWFJKO-UHFFFAOYSA-N 0.000 description 2
- 239000004801 Chlorinated PVC Substances 0.000 description 2
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 description 2
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 2
- 229920002521 macromolecule Polymers 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 229910052757 nitrogen Chemical group 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 229920002382 photo conductive polymer Polymers 0.000 description 2
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 2
- 238000009877 rendering Methods 0.000 description 2
- RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical compound NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 description 1
- SEGOAPVSMIXIQB-UHFFFAOYSA-N 1-ethenyl-3-(2-methyl-1,3-benzoxazol-6-yl)urea Chemical compound CC=1OC2=C(N1)C=CC(=C2)NC(=O)NC=C SEGOAPVSMIXIQB-UHFFFAOYSA-N 0.000 description 1
- UVHXEHGUEKARKZ-UHFFFAOYSA-N 1-ethenylanthracene Chemical compound C1=CC=C2C=C3C(C=C)=CC=CC3=CC2=C1 UVHXEHGUEKARKZ-UHFFFAOYSA-N 0.000 description 1
- HKPZFOCMKOCBJT-UHFFFAOYSA-N 1-phenothiazin-10-ylprop-2-en-1-one Chemical compound C1=CC=C2N(C(=O)C=C)C3=CC=CC=C3SC2=C1 HKPZFOCMKOCBJT-UHFFFAOYSA-N 0.000 description 1
- ZFYKDNCOQBBOST-UHFFFAOYSA-N 1-phenylbut-3-en-1-one Chemical compound C=CCC(=O)C1=CC=CC=C1 ZFYKDNCOQBBOST-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- QXBUYALKJGBACG-UHFFFAOYSA-N 10-methylphenothiazine Chemical compound C1=CC=C2N(C)C3=CC=CC=C3SC2=C1 QXBUYALKJGBACG-UHFFFAOYSA-N 0.000 description 1
- SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 description 1
- QHVBLSNVXDSMEB-UHFFFAOYSA-N 2-(diethylamino)ethyl prop-2-enoate Chemical compound CCN(CC)CCOC(=O)C=C QHVBLSNVXDSMEB-UHFFFAOYSA-N 0.000 description 1
- NNHTUFOCRUBQCF-UHFFFAOYSA-N 2-methyl-1,3-benzoxazol-6-amine Chemical compound C1=C(N)C=C2OC(C)=NC2=C1 NNHTUFOCRUBQCF-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- QWXUDYZXJKDYFG-UHFFFAOYSA-N 4,5-dimethyl-2,3-dihydro-1h-pyrrole Chemical compound CC1=C(C)NCC1 QWXUDYZXJKDYFG-UHFFFAOYSA-N 0.000 description 1
- RSSGMIIGVQRGDS-UHFFFAOYSA-N 4-[(4-hydroxyphenyl)-phenylmethyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)C1=CC=CC=C1 RSSGMIIGVQRGDS-UHFFFAOYSA-N 0.000 description 1
- RUKJCCIJLIMGEP-ONEGZZNKSA-N 4-dimethylaminocinnamaldehyde Chemical compound CN(C)C1=CC=C(\C=C\C=O)C=C1 RUKJCCIJLIMGEP-ONEGZZNKSA-N 0.000 description 1
- PWKBLDFFQPFWKQ-UHFFFAOYSA-N 9H-fluorene-3,6-disulfonic acid Chemical compound C1=CC(=CC=2C3=CC(=CC=C3CC12)S(=O)(=O)O)S(=O)(=O)O PWKBLDFFQPFWKQ-UHFFFAOYSA-N 0.000 description 1
- VOWWYDCFAISREI-UHFFFAOYSA-N Bisphenol AP Chemical compound C=1C=C(O)C=CC=1C(C=1C=CC(O)=CC=1)(C)C1=CC=CC=C1 VOWWYDCFAISREI-UHFFFAOYSA-N 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000004908 Emulsion polymer Substances 0.000 description 1
- 206010073306 Exposure to radiation Diseases 0.000 description 1
- HETCEOQFVDFGSY-UHFFFAOYSA-N Isopropenyl acetate Chemical compound CC(=C)OC(C)=O HETCEOQFVDFGSY-UHFFFAOYSA-N 0.000 description 1
- 239000005041 Mylar™ Substances 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- KYPYTERUKNKOLP-UHFFFAOYSA-N Tetrachlorobisphenol A Chemical compound C=1C(Cl)=C(O)C(Cl)=CC=1C(C)(C)C1=CC(Cl)=C(O)C(Cl)=C1 KYPYTERUKNKOLP-UHFFFAOYSA-N 0.000 description 1
- 125000004036 acetal group Chemical group 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- YMNKUHIVVMFOFO-UHFFFAOYSA-N anthracene-9-carbaldehyde Chemical compound C1=CC=C2C(C=O)=C(C=CC=C3)C3=CC2=C1 YMNKUHIVVMFOFO-UHFFFAOYSA-N 0.000 description 1
- 150000001454 anthracenes Chemical class 0.000 description 1
- WRUAHXANJKHFIL-UHFFFAOYSA-N benzene-1,3-disulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC(S(O)(=O)=O)=C1 WRUAHXANJKHFIL-UHFFFAOYSA-N 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- 150000001716 carbazoles Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N cyclobenzothiazole Natural products C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- WGXGKXTZIQFQFO-CMDGGOBGSA-N ethenyl (e)-3-phenylprop-2-enoate Chemical compound C=COC(=O)\C=C\C1=CC=CC=C1 WGXGKXTZIQFQFO-CMDGGOBGSA-N 0.000 description 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
- WOLATMHLPFJRGC-UHFFFAOYSA-N furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1 WOLATMHLPFJRGC-UHFFFAOYSA-N 0.000 description 1
- 235000010985 glycerol esters of wood rosin Nutrition 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- TWUPWHYFUPQNQD-UHFFFAOYSA-N n-(2-methyl-1,3-benzothiazol-6-yl)prop-2-enamide Chemical compound C1=C(NC(=O)C=C)C=C2SC(C)=NC2=C1 TWUPWHYFUPQNQD-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229960005130 niridazole Drugs 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 1
- GJSGGHOYGKMUPT-UHFFFAOYSA-N phenoxathiine Chemical compound C1=CC=C2OC3=CC=CC=C3SC2=C1 GJSGGHOYGKMUPT-UHFFFAOYSA-N 0.000 description 1
- 229920002006 poly(N-vinylimidazole) polymer Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920002102 polyvinyl toluene Polymers 0.000 description 1
- BGUWFUQJCDRPTL-UHFFFAOYSA-N pyridine-4-carbaldehyde Chemical compound O=CC1=CC=NC=C1 BGUWFUQJCDRPTL-UHFFFAOYSA-N 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H04—ELECTRIC COMMUNICATION TECHNIQUE
- H04N—PICTORIAL COMMUNICATION, e.g. TELEVISION
- H04N5/00—Details of television systems
- H04N5/76—Television signal recording
- H04N5/80—Television signal recording using electrostatic recording
- H04N5/82—Television signal recording using electrostatic recording using deformable thermoplastic recording medium
-
- 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
- G03G13/04—Exposing, i.e. imagewise exposure by optically projecting the original image on a photoconductive recording material
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G16/00—Electrographic processes using deformation of thermoplastic layers; Apparatus therefor
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/022—Layers for surface-deformation imaging, e.g. frost imaging
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/07—Polymeric photoconductive materials
- G03G5/071—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/07—Polymeric photoconductive materials
- G03G5/071—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G5/072—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising pending monoamine groups
- G03G5/073—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising pending monoamine groups comprising pending carbazole groups
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/07—Polymeric photoconductive materials
- G03G5/071—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G5/072—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising pending monoamine groups
- G03G5/0732—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising pending monoamine groups comprising pending alkenylarylamine
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B11/00—Recording on or reproducing from the same record carrier wherein for these two operations the methods are covered by different main groups of groups G11B3/00 - G11B7/00 or by different subgroups of group G11B9/00; Record carriers therefor
- G11B11/16—Recording on or reproducing from the same record carrier wherein for these two operations the methods are covered by different main groups of groups G11B3/00 - G11B7/00 or by different subgroups of group G11B9/00; Record carriers therefor using recording by mechanical cutting, deforming or pressing
- G11B11/18—Recording on or reproducing from the same record carrier wherein for these two operations the methods are covered by different main groups of groups G11B3/00 - G11B7/00 or by different subgroups of group G11B9/00; Record carriers therefor using recording by mechanical cutting, deforming or pressing with reproducing by optical means
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B9/00—Recording or reproducing using a method not covered by one of the main groups G11B3/00 - G11B7/00; Record carriers therefor
- G11B9/08—Recording or reproducing using a method not covered by one of the main groups G11B3/00 - G11B7/00; Record carriers therefor using electrostatic charge injection; Record carriers therefor
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11C—STATIC STORES
- G11C13/00—Digital stores characterised by the use of storage elements not covered by groups G11C11/00, G11C23/00, or G11C25/00
- G11C13/04—Digital stores characterised by the use of storage elements not covered by groups G11C11/00, G11C23/00, or G11C25/00 using optical elements ; using other beam accessed elements, e.g. electron or ion beam
- G11C13/048—Digital stores characterised by the use of storage elements not covered by groups G11C11/00, G11C23/00, or G11C25/00 using optical elements ; using other beam accessed elements, e.g. electron or ion beam using other optical storage elements
Definitions
- This invention relates to novel methods for recording and reproducing information.
- thermoplastic tape According to a recently proposed method (W. E. Glenn, Journal of Applied Physics, volume 30, pages 1870-1873, 1959), information is recorded in the form of deformations or ripples in the surface of a thermoplastic tape.
- the information can be detected optically by projecting light through these ripples to form a visible image on a screen.
- the tape consists of a high melting base film coated with a metallic conducting layer which is in turn coated with the low melting thermoplastic material.
- an electron gun information can be written on the surface of the thermoplastic layer in the form of a charge pattern.
- electrostatic forces between the charge pattern and the metallic, conductive layer caused deformations or ripples in the tape surface.
- thermoplastic material freezes these deformations, thus yielding a permanent record of the recorded information.
- a modi- -fied Schlieren optical system is employed to project the recorded information on a screen.
- the tape may be erased for reuse by heating the film above its melting point for a period of time suificient to allow the charge pattern to drain away and to allow the surface tension of the thermoplastic layer to smooth out the deformations.
- thermoplastic recording process will be employed to indicate the process described.
- thermoplastic recordation of information on a photoconductive, polymeric material by effecting the thermoplastic recordation of information on a photoconductive, polymeric material.
- the method of the present invention utilizes a low melting, thermoplastic, photoconductive, polymeric material.
- the tape consists of a high melting base 3,441,947 Patented Apr. 29, 1969 ice film coated with a thin, conductive layer which is in turn coated with a photoconductive polymeric layer.
- the use of a photoconductive, polymeric material enables simpler, more efficient recording apparatus than has been heretofore possible in thermoplastic recording processes.
- a uniform electrostatic charge is placed on the surface of the photoconductive layer of the thermoplastic tape by exposure to a charging device, such as a corona generating device.
- a charging device such as a corona generating device.
- the charge in the exposed areas of the tape is dissipated by virtue of the selective increase in conductivity in these areas.
- the tape then contains an image in the form of a charge pattern.
- the tape is then further processed in the manner according to Glenn by first, heating the tape above the melting point of the photoconductive layer to allow deformations or ripples to form in the surface of the tape; second, cooling the tape to freeze these ripples into a permanent record and third, optically detecting the recorded information in a suitable projection apparatus.
- the method of the present invention constitutes an improvement over the prior art process.
- the method of the present invention merely involves simple charging and exposure operations which can be carried out with simple equipment under atmospheric pressure condition.
- the present method is therefore less expensive, more efiicient and less complicated than the prior art methods.
- Photoconductive polymeric materials useful in the process of the present invention include any macromolecular substance or any mixture of macromolecular substances which on exposure to radiation of suitable wavelength exhibits an increase in conductivity.
- the following classes of polymeric substances have been found to be especially useful:
- Vinyl polymers with acetal groups such as, e.g.,
- A represents a divalent radical such as NHCO, NHCONH or 0C0;
- R represents a hydrogen atom or a substituent of the aromatic nucleus such as methoxy group
- R represents a hydrogen atom or a methyl group, such as, e.g.,
- Poly (4-methacrylyloxy) -stilbene Poly p- N'-vinylureido -stilbene] Poly [4-methoxy-4'- (N-acrylyl -aminostilbene] Copolymer of vinyl acetate and p-(N-vinylureido)-stilbene,
- Y represents an oxygen atom or a sulfur atom
- R represents a hydrogen atom or a methyl group, such as, e.g.,
- A represents a divalent radical such as or a single bond
- Q and Q each represents a hydrogen atom, a methyl radical, a nitro group, a phenyl group, a substituted phenyl group, or form together the atoms necessary to close a ring;
- R represents a hydrogen atom or a methyl group
- A represents a single bond or CH CH OCO;
- Q Q and Q each represents a hydrogen atom or a phenyl nucleus; and
- R represents a hydrogen atom or a methyl group, such 4 as, e.g.,
- Y represents a single bond, 3.
- sulphur atom or a carbonyl Z represents a carbonyl group or a nitrogen atom substituted by a lower alkyl radical; and R represents a hydrogen atom or a methyl group, such as, e.g.,
- Nitrated terpolymer (vinyl acetate/styrene/maleic anhydride),
- A represents a single bond, or a divalent organic radical such as, e.g.,
- R and R each represents a hydrogen atom or a lower alkyl radical such as, e.g., a methyl radical;
- Z represents a sulphur atom or a single bond;
- Z represents a rnethine group or a nitrogen atom;
- Q and Q together represent the atoms necessary to complete an aromatic nucleus; and
- Q and Q together represent the atoms necessary to complete an aromatic nucleus, such as, e.g.,
- A represents an aromatic nucleus such as, e.g., a benzene nucleus or a heterocyclic nucleus such as a carbazole nucleus;
- B represents an aromatic nucleus such as e.g., a benzene, a naphthalene or anthracene nucleus, or a heterocyclic nucleus such as, e.g., a carbazole, phenothiazine or quinoline nucleus;
- R represents a hydrogen atom or a lower alkyl radical such as, e.g., a methyl radical
- n and m each represents a positive integer from 1 to 2
- Polyesters such as, e.g.,
- Copolyester of terephthalic acid and diphenyl-p,p'-disulphonic acid with 2,2-di(4-hydroxyphenyl)-propane Copolyester of diphenyl-p,p'-disulph0nic acid and diphenyl ether-p,p'-disulphonic acid with 2,2-di(4-hydroxyphenyl)-propane and 2,2-di(4-hydroxyphenyl)-butane
- Copolyester of 2,2-di(4-hydroxy-3,S-dibromophenyl)-propane and 2,2-di(4-hydroxyphenyl)-propane with isophthalic acid isophthalic acid.
- Copolyester of fluorene-3,6-disulphonic acid and diphenylp,p-disulphonic acid with 2,2-di(4-hydroxyphenyl)- propane
- Cellulose-derivatives such as, e.g., Cellulose-aceto-N-phenylcarbamate, Cellulose-acetocinnamate.
- thermoplastic photoconductive polymers may be employed in combination with substances increasing their sensitivity, such substances are, e.g., mentioned in the British patent specifications 964,871-964,875 and 964,877.
- the tape may consist solely of self-supported photoconductive polymeric material or it may consist of the photoconductive polymeric material coated upon a high melting base film such as one sold under the trademark Mylar or Cronar, for example. In either case, it is necessary that the photoconductive polymeric layer be in intimate surface contact with a conductive backing. Any metallic or similar conductor, such as copper or aluminium for example, may be employed. Should the tape comprise a self-supporting photoconductive polymeric material, its thickness should be sufiicient to allow heating of the surface on which information is recorded only to a fraction of the thickness, so that the tape will remain in a selfsupporting state. Unually tapes of a thickness of 10 to p. will suffice.
- Recordation of information can be achieved simply, economically and efiiciently by any method involving exposure of the photoconductive material to a pattern of electro-magnetic radiation rendering the polymer conductive and by bringing about a charge condition of the unexposed areas.
- the recording medium may be uniformly charged by passing thereover a corona generating device. Either a positive or negative electrostatic charge may be laid upon the film. Subsequently, the charged film is image-wise exposed to electromagnetic radiation of suitable wavelength. The radiation struck areas of the photoconductor, being rendered conductive thereby, charge is carried oil. The unexposed areas of the film remain charged.
- the photoconductive film may first be exposed image-wise to electromagnetic radiation, thus rendering the light struck areas conductive and subsequently, uniformly charged with a corona generating device. No charge will be laid down on the conductive, radiation struck areas of the film and an image comparable to that produced by the method described above will occur.
- Reproduction of the recorded image may be accomplished by means of any conventional optical projection system.
- any conventional optical projection system For example, a system based upon the principles of phase diffraction grating whereby visible light, diffracted by the ripples in the photoconductive medium is permitted to shine upon a screen while light which passes through smooth, nondeformed areas of the film is not permitted to shine upon the screen, a visible reproduction of the recorded information is produced.
- the recorded electrostatic latent image in the photoconductive layer should be built up line-wise by exposure, e.g., to a light spot of a flying spot scanner. Such a method will yield a ripple image adapted for reproduction in a phase diffraction system. It is to be understood, however, that any suitable and conventional optical projection system may be employed to reproduce the ripple image.
- thermoplastic layer of the following composition:
- the dried photoconductive layer has a thickness of 1.5 to 2 microns.
- the material is charged by means of a corona generating device and a latent electrostatic record of information is created by selectively carrying otf electric charge from the material using a light spot (flying spot scanner).
- the material is then heated to the melting point of the polymeric material and after the deformations have set in according to the charge pattern, the material is cooled to freeze the deformations.
- Reproduction of the image is accomplished by employing projection apparatus such as that described by W. E. Glenn.
- the material is erased by melting the polymeric material above its melting point while exposing it to light. Subsequent, recordations on the erased tape by this same described method, produced excellent images.
- a process for recording optical information on a deformable layer in the form of a relief pattern which comprises electrostatically charging a layer of a thermoplastic photoconductive polymeric layer superimposed upon a layer of conductive material before or after said layer is subjected to electromagnetic radiation to which said photoconductive layer is sensitive in a pattern according to said information to be recorded so as to produce on said layer an electrostatic charge pattern in accordance with the information to be recorded, heating said material to a degree suflicient to soften at least the surface layer of the polymeric said layer whereby said softened surface layer is deformed physically under the influence of the electrostatic forces existing between the charge pattern at the surface of said photoconductive layer and said conductive layer, and cooling said heated layer to fix the deformations therein.
- polymeric layer additionally contains a radiation sensitive substance.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Multimedia (AREA)
- Signal Processing (AREA)
- Photoreceptors In Electrophotography (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1745260A GB964880A (en) | 1960-05-17 | 1960-05-17 | Improvements in or relating to electrostatic recording |
GB2348660A GB964881A (en) | 1960-05-17 | 1960-05-17 | Improvements in or relating to electrostatic records |
Publications (1)
Publication Number | Publication Date |
---|---|
US3441947A true US3441947A (en) | 1969-04-29 |
Family
ID=26252692
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US3441947D Expired - Lifetime US3441947A (en) | 1960-05-17 | 1965-10-07 | Thermoplastic recording process |
Country Status (7)
Country | Link |
---|---|
US (1) | US3441947A (enrdf_load_stackoverflow) |
BE (1) | BE603891A (enrdf_load_stackoverflow) |
DE (1) | DE1424387A1 (enrdf_load_stackoverflow) |
FR (1) | FR1314384A (enrdf_load_stackoverflow) |
GB (2) | GB964881A (enrdf_load_stackoverflow) |
NL (1) | NL264844A (enrdf_load_stackoverflow) |
SE (2) | SE311180B (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4233380A (en) * | 1972-03-17 | 1980-11-11 | Hoechst Aktiengesellschaft | Process for shaping a thermoplastic layer |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2896507A (en) * | 1952-04-16 | 1959-07-28 | Foerderung Forschung Gmbh | Arrangement for amplifying the light intensity of an optically projected image |
US3055006A (en) * | 1961-01-24 | 1962-09-18 | Ibm | High density, erasable optical image recorder |
US3284196A (en) * | 1962-10-11 | 1966-11-08 | Ibm | Apparatus and method for electric recording |
-
0
- NL NL264844D patent/NL264844A/xx unknown
- BE BE603891D patent/BE603891A/xx unknown
-
1960
- 1960-05-17 GB GB2348660A patent/GB964881A/en not_active Expired
- 1960-05-17 GB GB1745260A patent/GB964880A/en not_active Expired
-
1961
- 1961-05-15 SE SE509661A patent/SE311180B/xx unknown
- 1961-05-16 DE DE19611424387 patent/DE1424387A1/de active Pending
- 1961-05-17 FR FR862083A patent/FR1314384A/fr not_active Expired
-
1964
- 1964-11-23 SE SE1412764A patent/SE315312B/xx unknown
-
1965
- 1965-10-07 US US3441947D patent/US3441947A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2896507A (en) * | 1952-04-16 | 1959-07-28 | Foerderung Forschung Gmbh | Arrangement for amplifying the light intensity of an optically projected image |
US3055006A (en) * | 1961-01-24 | 1962-09-18 | Ibm | High density, erasable optical image recorder |
US3284196A (en) * | 1962-10-11 | 1966-11-08 | Ibm | Apparatus and method for electric recording |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4233380A (en) * | 1972-03-17 | 1980-11-11 | Hoechst Aktiengesellschaft | Process for shaping a thermoplastic layer |
Also Published As
Publication number | Publication date |
---|---|
FR1314384A (fr) | 1963-01-11 |
BE603891A (enrdf_load_stackoverflow) | 1900-01-01 |
SE315312B (enrdf_load_stackoverflow) | 1969-09-29 |
DE1424387A1 (de) | 1969-01-16 |
SE311180B (enrdf_load_stackoverflow) | 1969-06-02 |
GB964880A (en) | 1964-07-22 |
NL264844A (enrdf_load_stackoverflow) | 1900-01-01 |
GB964881A (en) | 1964-07-22 |
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