FI56646C - Tryckkaensligt kopieringssystem - Google Patents
Tryckkaensligt kopieringssystem Download PDFInfo
- Publication number
- FI56646C FI56646C FI289372A FI289372A FI56646C FI 56646 C FI56646 C FI 56646C FI 289372 A FI289372 A FI 289372A FI 289372 A FI289372 A FI 289372A FI 56646 C FI56646 C FI 56646C
- Authority
- FI
- Finland
- Prior art keywords
- color
- solvent
- generating agent
- acidic
- solvents
- Prior art date
Links
- 239000002904 solvent Substances 0.000 claims description 72
- 239000003795 chemical substances by application Substances 0.000 claims description 34
- 239000007788 liquid Substances 0.000 claims description 19
- 230000002378 acidificating effect Effects 0.000 claims description 17
- -1 ethylphenyl Chemical group 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 230000006835 compression Effects 0.000 claims description 7
- 238000007906 compression Methods 0.000 claims description 7
- WNZQDUSMALZDQF-UHFFFAOYSA-N isobenzofuranone Natural products C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 claims description 7
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 6
- 239000004927 clay Substances 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims description 2
- 235000010290 biphenyl Nutrition 0.000 claims description 2
- 239000004305 biphenyl Substances 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 229920000620 organic polymer Polymers 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- 125000005023 xylyl group Chemical group 0.000 claims description 2
- 230000001235 sensitizing effect Effects 0.000 claims 1
- 239000000975 dye Substances 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 15
- 239000000126 substance Substances 0.000 description 15
- 239000003086 colorant Substances 0.000 description 9
- 238000011161 development Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 239000002775 capsule Substances 0.000 description 8
- 239000003085 diluting agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 6
- 238000005562 fading Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000000376 reactant Substances 0.000 description 4
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 239000000295 fuel oil Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 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 3
- 239000004006 olive oil Substances 0.000 description 3
- 235000008390 olive oil Nutrition 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical compound C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 150000002596 lactones Chemical class 0.000 description 2
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical class COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XLWCIHPMASUXPI-UHFFFAOYSA-N 1,1'-(propane-1,2-diyl)dibenzene Chemical compound C=1C=CC=CC=1C(C)CC1=CC=CC=C1 XLWCIHPMASUXPI-UHFFFAOYSA-N 0.000 description 1
- WSSNQXJVTQOUMV-UHFFFAOYSA-N 1,2-dibenzyl-3,4-dimethylbenzene Chemical group C=1C=CC=CC=1CC1=C(C)C(C)=CC=C1CC1=CC=CC=C1 WSSNQXJVTQOUMV-UHFFFAOYSA-N 0.000 description 1
- WBQIISMZRBZAHJ-UHFFFAOYSA-N 1,2-dibenzyl-3-ethylbenzene Chemical compound C=1C=CC=CC=1CC=1C(CC)=CC=CC=1CC1=CC=CC=C1 WBQIISMZRBZAHJ-UHFFFAOYSA-N 0.000 description 1
- PKQYSCBUFZOAPE-UHFFFAOYSA-N 1,2-dibenzyl-3-methylbenzene Chemical compound C=1C=CC=CC=1CC=1C(C)=CC=CC=1CC1=CC=CC=C1 PKQYSCBUFZOAPE-UHFFFAOYSA-N 0.000 description 1
- ADGBOWGNWOIBSB-UHFFFAOYSA-N 1,2-dibenzyl-3-propan-2-ylbenzene Chemical compound C=1C=CC=CC=1CC=1C(C(C)C)=CC=CC=1CC1=CC=CC=C1 ADGBOWGNWOIBSB-UHFFFAOYSA-N 0.000 description 1
- BJMUOUXGBFNLSN-UHFFFAOYSA-N 1,2-dimethylindole Chemical compound C1=CC=C2N(C)C(C)=CC2=C1 BJMUOUXGBFNLSN-UHFFFAOYSA-N 0.000 description 1
- KRXXWINWRGUIBJ-UHFFFAOYSA-N 1,3,3-trimethyl-2h-indole Chemical compound C1=CC=C2N(C)CC(C)(C)C2=C1 KRXXWINWRGUIBJ-UHFFFAOYSA-N 0.000 description 1
- IOXAUPNPMJKSKQ-UHFFFAOYSA-N 1-benzyl-2,3-dimethylbenzene Chemical group CC1=CC=CC(CC=2C=CC=CC=2)=C1C IOXAUPNPMJKSKQ-UHFFFAOYSA-N 0.000 description 1
- VXVRAGONKSWKEZ-UHFFFAOYSA-N 3,3-bis(1,2-dimethylindol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC=C2C(C3(C4=CC=CC=C4C(=O)O3)C3=C(N(C4=CC=CC=C43)C)C)=C(C)N(C)C2=C1 VXVRAGONKSWKEZ-UHFFFAOYSA-N 0.000 description 1
- FNVUVCSZVQWREE-UHFFFAOYSA-N 3,3-bis(2-phenyl-1h-indol-3-yl)-2-benzofuran-1-one Chemical class C12=CC=CC=C2C(=O)OC1(C=1C2=CC=CC=C2NC=1C=1C=CC=CC=1)C(C1=CC=CC=C1N1)=C1C1=CC=CC=C1 FNVUVCSZVQWREE-UHFFFAOYSA-N 0.000 description 1
- ABJAMKKUHBSXDS-UHFFFAOYSA-N 3,3-bis(6-amino-1,4-dimethylcyclohexa-2,4-dien-1-yl)-2-benzofuran-1-one Chemical compound C1=CC(C)=CC(N)C1(C)C1(C2(C)C(C=C(C)C=C2)N)C2=CC=CC=C2C(=O)O1 ABJAMKKUHBSXDS-UHFFFAOYSA-N 0.000 description 1
- KNNGWESDZOFDIV-UHFFFAOYSA-N 3,3-bis[4-(methylamino)phenyl]-2-benzofuran-1-one Chemical compound C1=CC(NC)=CC=C1C1(C=2C=CC(NC)=CC=2)C2=CC=CC=C2C(=O)O1 KNNGWESDZOFDIV-UHFFFAOYSA-N 0.000 description 1
- MLJCAUJSTUJCIN-UHFFFAOYSA-N 3-(1,2-dimethylindol-3-yl)-3-(2-methyl-1h-indol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC=C2C(C3(C4=CC=CC=C4C(=O)O3)C=3C4=CC=CC=C4NC=3C)=C(C)N(C)C2=C1 MLJCAUJSTUJCIN-UHFFFAOYSA-N 0.000 description 1
- LHNYVYZSXVHNDA-UHFFFAOYSA-N 3-(1h-indol-3-yl)-3-phenyl-2-benzofuran-1-one Chemical class C12=CC=CC=C2C(=O)OC1(C=1C2=CC=CC=C2NC=1)C1=CC=CC=C1 LHNYVYZSXVHNDA-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- MQJTWPAGXWPEKU-UHFFFAOYSA-N 3-[4-(dimethylamino)phenyl]-3-(1,2-dimethylindol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC(N(C)C)=CC=C1C1(C=2C3=CC=CC=C3N(C)C=2C)C2=CC=CC=C2C(=O)O1 MQJTWPAGXWPEKU-UHFFFAOYSA-N 0.000 description 1
- OPLBFHRSNKSMKD-UHFFFAOYSA-N 3H-2-benzofuran-1-one 1H-indole Chemical class C1=CC=C2NC=CC2=C1.C1=CC=C2C(=O)OCC2=C1 OPLBFHRSNKSMKD-UHFFFAOYSA-N 0.000 description 1
- RNRINRUTVAFUCG-UHFFFAOYSA-N 5-(dimethylamino)-3,3-bis(1,2-dimethylindol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC=C2C(C3(C=4C5=CC=CC=C5N(C)C=4C)OC(=O)C4=CC=C(C=C43)N(C)C)=C(C)N(C)C2=C1 RNRINRUTVAFUCG-UHFFFAOYSA-N 0.000 description 1
- UJIFZLCSKDRXCZ-UHFFFAOYSA-N 6-(dimethylamino)-3-[4-(dimethylamino)phenyl]-3-(1-methylpyrrol-2-yl)-2-benzofuran-1-one Chemical compound C1=CC(N(C)C)=CC=C1C1(C=2N(C=CC=2)C)C2=CC=C(N(C)C)C=C2C(=O)O1 UJIFZLCSKDRXCZ-UHFFFAOYSA-N 0.000 description 1
- TYIHCISAZQHKHT-UHFFFAOYSA-N 6-(dimethylamino)-3-[4-(dimethylamino)phenyl]-3h-2-benzofuran-1-one Chemical compound C1=CC(N(C)C)=CC=C1C1C2=CC=C(N(C)C)C=C2C(=O)O1 TYIHCISAZQHKHT-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical class CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 206010024769 Local reaction Diseases 0.000 description 1
- 240000002853 Nelumbo nucifera Species 0.000 description 1
- 235000006508 Nelumbo nucifera Nutrition 0.000 description 1
- 235000006510 Nelumbo pentapetala Nutrition 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- ZKURGBYDCVNWKH-UHFFFAOYSA-N [3,7-bis(dimethylamino)phenothiazin-10-yl]-phenylmethanone Chemical group C12=CC=C(N(C)C)C=C2SC2=CC(N(C)C)=CC=C2N1C(=O)C1=CC=CC=C1 ZKURGBYDCVNWKH-UHFFFAOYSA-N 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000006177 alkyl benzyl group Chemical group 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical class CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011981 development test Methods 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 210000002257 embryonic structure Anatomy 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 210000000003 hoof Anatomy 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000011005 laboratory method Methods 0.000 description 1
- 239000010699 lard oil Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 150000007517 lewis acids Chemical class 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
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229960001047 methyl salicylate Drugs 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 125000005506 phthalide group Chemical group 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000001911 terphenyls Chemical class 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 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
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
- B41M5/165—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components characterised by the use of microcapsules; Special solvents for incorporating the ingredients
- B41M5/1655—Solvents
Landscapes
- Color Printing (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19105371A | 1971-10-20 | 1971-10-20 | |
| US19105371 | 1971-10-20 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| FI56646B FI56646B (fi) | 1979-11-30 |
| FI56646C true FI56646C (fi) | 1980-03-10 |
Family
ID=22703943
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI289372A FI56646C (fi) | 1971-10-20 | 1972-10-19 | Tryckkaensligt kopieringssystem |
Country Status (11)
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS604797B2 (ja) * | 1975-05-02 | 1985-02-06 | 呉羽化学工業株式会社 | 感圧複写紙用染料溶剤 |
| US4130299A (en) * | 1977-09-12 | 1978-12-19 | Monsanto Company | Low-odor dye solvents for pressure-sensitive copying systems |
| JPS5634495A (en) * | 1979-08-31 | 1981-04-06 | Kureha Chem Ind Co Ltd | Pressure sensitive copying paper |
| JPS5711085A (en) * | 1980-06-25 | 1982-01-20 | Nippon Petrochem Co Ltd | Recording material |
| IT1136651B (it) * | 1981-06-04 | 1986-09-03 | Caffaro Spa Ind Chim | Solvente per coloranti in carte autocopianti |
| JPS6141593A (ja) * | 1984-08-06 | 1986-02-27 | Nippon Petrochem Co Ltd | 感圧紙染料用溶剤 |
| DE3633116A1 (de) * | 1986-09-30 | 1988-04-07 | Feldmuehle Ag | Druckempfindliches aufzeichnungsmaterial |
| JP2946233B2 (ja) * | 1990-07-10 | 1999-09-06 | 日本石油化学株式会社 | 感圧複写材料 |
| DE4407813C1 (de) * | 1994-03-09 | 1995-10-26 | Feldmuehle Ag Stora | Mikrokapseldispersion |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3016308A (en) * | 1957-08-06 | 1962-01-09 | Moore Business Forms Inc | Recording paper coated with microscopic capsules of coloring material, capsules and method of making |
| GB1053935A (enrdf_load_stackoverflow) * | 1964-08-27 | 1900-01-01 | ||
| DE1960868A1 (de) * | 1968-12-09 | 1970-06-18 | Sandoz Ag | Faerben und Bedrucken von Gebilden aus hydrophoben,organischen Hochpolymeren |
| JPS5016967B1 (enrdf_load_stackoverflow) * | 1971-08-04 | 1975-06-17 |
-
0
- BE BE790321D patent/BE790321A/xx not_active IP Right Cessation
-
1972
- 1972-10-16 ES ES407662A patent/ES407662A1/es not_active Expired
- 1972-10-19 FI FI289372A patent/FI56646C/fi active
- 1972-10-19 CH CH1531172A patent/CH567938A5/xx not_active IP Right Cessation
- 1972-10-19 FR FR7237099A patent/FR2157587A5/fr not_active Expired
- 1972-10-19 IT IT3068072A patent/IT969706B/it active
- 1972-10-19 DE DE19722251350 patent/DE2251350C2/de not_active Expired
- 1972-10-19 SE SE1347472A patent/SE385281B/xx unknown
- 1972-10-19 BR BR732972A patent/BR7207329D0/pt unknown
- 1972-10-19 GB GB4825572A patent/GB1406107A/en not_active Expired
- 1972-10-19 JP JP47104070A patent/JPS4849506A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| FR2157587A5 (enrdf_load_stackoverflow) | 1973-06-01 |
| IT969706B (it) | 1974-04-10 |
| JPS4849506A (enrdf_load_stackoverflow) | 1973-07-12 |
| GB1406107A (en) | 1975-09-17 |
| DE2251350A1 (de) | 1973-04-26 |
| SE385281B (sv) | 1976-06-21 |
| CH567938A5 (enrdf_load_stackoverflow) | 1975-10-15 |
| ES407662A1 (es) | 1976-02-16 |
| FI56646B (fi) | 1979-11-30 |
| BR7207329D0 (pt) | 1973-09-27 |
| DE2251350C2 (de) | 1990-02-15 |
| BE790321A (fr) | 1973-04-19 |
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