JPS645553B2 - - Google Patents
Info
- Publication number
- JPS645553B2 JPS645553B2 JP56126576A JP12657681A JPS645553B2 JP S645553 B2 JPS645553 B2 JP S645553B2 JP 56126576 A JP56126576 A JP 56126576A JP 12657681 A JP12657681 A JP 12657681A JP S645553 B2 JPS645553 B2 JP S645553B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- color
- metal
- coloring
- phenyl
- 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
Links
- 239000013522 chelant Substances 0.000 claims description 28
- 229910052751 metal Inorganic materials 0.000 claims description 26
- 239000002184 metal Substances 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 23
- 238000004040 coloring Methods 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 14
- 239000003960 organic solvent Substances 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- -1 spiropyran series Chemical class 0.000 description 27
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 229910021645 metal ion Inorganic materials 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 238000011161 development Methods 0.000 description 6
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 5
- 239000000370 acceptor Substances 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- YTVQIZRDLKWECQ-UHFFFAOYSA-N 2-benzoylcyclohexan-1-one Chemical compound C=1C=CC=CC=1C(=O)C1CCCCC1=O YTVQIZRDLKWECQ-UHFFFAOYSA-N 0.000 description 4
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 4
- 239000002775 capsule Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 125000005594 diketone group Chemical group 0.000 description 4
- PGCYJKDJSLVDGX-UHFFFAOYSA-N dodecane-2,4-dione Chemical compound CCCCCCCCC(=O)CC(C)=O PGCYJKDJSLVDGX-UHFFFAOYSA-N 0.000 description 4
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 4
- 229960004889 salicylic acid Drugs 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- GNPWYHFXSMINJQ-UHFFFAOYSA-N 1,2-dimethyl-3-(1-phenylethyl)benzene Chemical compound C=1C=CC(C)=C(C)C=1C(C)C1=CC=CC=C1 GNPWYHFXSMINJQ-UHFFFAOYSA-N 0.000 description 2
- GPYKJDYMMUIUFG-UHFFFAOYSA-N 1-(2-Furanyl)-1,3-butanedione Chemical compound CC(=O)CC(=O)C1=CC=CO1 GPYKJDYMMUIUFG-UHFFFAOYSA-N 0.000 description 2
- ZKPDXFCMHFRNQC-UHFFFAOYSA-N 1-pyridin-2-ylbutane-1,3-dione Chemical compound CC(=O)CC(=O)C1=CC=CC=N1 ZKPDXFCMHFRNQC-UHFFFAOYSA-N 0.000 description 2
- VZRNDOSIHXJXCH-UHFFFAOYSA-N 2,4-Heptadecanedione Chemical compound CCCCCCCCCCCCCC(=O)CC(C)=O VZRNDOSIHXJXCH-UHFFFAOYSA-N 0.000 description 2
- OFMOAXULFCSTKC-UHFFFAOYSA-N 3,5-dimethylheptane-2,4,6-trione Chemical compound CC(=O)C(C)C(=O)C(C)C(C)=O OFMOAXULFCSTKC-UHFFFAOYSA-N 0.000 description 2
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- VHNFAQLOVBWGGB-UHFFFAOYSA-N benzhydrylbenzene;3h-2-benzofuran-1-one Chemical class C1=CC=C2C(=O)OCC2=C1.C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 VHNFAQLOVBWGGB-UHFFFAOYSA-N 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
- NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical compound C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 150000002085 enols Chemical group 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000007903 gelatin capsule Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- MUYHXSSRXORHIS-UHFFFAOYSA-N 1,1,1,2,2-pentafluoroheptane-3,5-dione Chemical compound CCC(=O)CC(=O)C(F)(F)C(F)(F)F MUYHXSSRXORHIS-UHFFFAOYSA-N 0.000 description 1
- KMIUUDQKENYYMD-UHFFFAOYSA-N 1,8-diphenyloctane-1,3,6,8-tetrone Chemical compound C=1C=CC=CC=1C(=O)CC(=O)CCC(=O)CC(=O)C1=CC=CC=C1 KMIUUDQKENYYMD-UHFFFAOYSA-N 0.000 description 1
- GDVHNOIEAQDUHT-UHFFFAOYSA-N 1-(furan-2-yl)-5-methylhexane-1,3-dione Chemical compound CC(C)CC(=O)CC(=O)C1=CC=CO1 GDVHNOIEAQDUHT-UHFFFAOYSA-N 0.000 description 1
- CKVCCVWLSUKOIG-UHFFFAOYSA-N 1-[4-[4-(3-oxo-3-phenylpropanoyl)phenyl]phenyl]-3-phenylpropane-1,3-dione Chemical group C=1C=CC=CC=1C(=O)CC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)CC(=O)C1=CC=CC=C1 CKVCCVWLSUKOIG-UHFFFAOYSA-N 0.000 description 1
- DBTNGSXXORPPCW-UHFFFAOYSA-N 1-chloro-1,1-difluoroheptane-2,4-dione Chemical compound CCCC(=O)CC(=O)C(F)(F)Cl DBTNGSXXORPPCW-UHFFFAOYSA-N 0.000 description 1
- KLCGMDWRXACELA-UHFFFAOYSA-N 1-cyclopropylbutane-1,3-dione Chemical compound CC(=O)CC(=O)C1CC1 KLCGMDWRXACELA-UHFFFAOYSA-N 0.000 description 1
- CVBUKMMMRLOKQR-UHFFFAOYSA-N 1-phenylbutane-1,3-dione Chemical compound CC(=O)CC(=O)C1=CC=CC=C1 CVBUKMMMRLOKQR-UHFFFAOYSA-N 0.000 description 1
- PWYYHTLZMQHPLP-UHFFFAOYSA-N 1-phenylhexane-1,3,5-trione Chemical compound CC(=O)CC(=O)CC(=O)C1=CC=CC=C1 PWYYHTLZMQHPLP-UHFFFAOYSA-N 0.000 description 1
- WBMJETLNTZLTFE-UHFFFAOYSA-N 1-phenylhexane-1,3-dione Chemical compound CCCC(=O)CC(=O)C1=CC=CC=C1 WBMJETLNTZLTFE-UHFFFAOYSA-N 0.000 description 1
- NKXMBTKMOVMBPH-UHFFFAOYSA-N 1-phenylpentane-1,3-dione Chemical compound CCC(=O)CC(=O)C1=CC=CC=C1 NKXMBTKMOVMBPH-UHFFFAOYSA-N 0.000 description 1
- KFBXUKHERGLHLG-UHFFFAOYSA-N 2,4-Nonanedione Chemical compound CCCCCC(=O)CC(C)=O KFBXUKHERGLHLG-UHFFFAOYSA-N 0.000 description 1
- OEKATORRSPXJHE-UHFFFAOYSA-N 2-acetylcyclohexan-1-one Chemical compound CC(=O)C1CCCCC1=O OEKATORRSPXJHE-UHFFFAOYSA-N 0.000 description 1
- XETGXVFFSABOGK-UHFFFAOYSA-N 2-butanoylcyclohexan-1-one Chemical compound CCCC(=O)C1CCCCC1=O XETGXVFFSABOGK-UHFFFAOYSA-N 0.000 description 1
- MVSJGHNTDUMJJZ-UHFFFAOYSA-N 2-hexanoylcyclohexan-1-one Chemical compound CCCCCC(=O)C1CCCCC1=O MVSJGHNTDUMJJZ-UHFFFAOYSA-N 0.000 description 1
- UYMBCDOGDVGEFA-UHFFFAOYSA-N 3-(1h-indol-2-yl)-3h-2-benzofuran-1-one Chemical class C12=CC=CC=C2C(=O)OC1C1=CC2=CC=CC=C2N1 UYMBCDOGDVGEFA-UHFFFAOYSA-N 0.000 description 1
- BGVBGAIWXAXBLP-UHFFFAOYSA-N 3-Methyl-2,4-nonanedione Chemical compound CCCCCC(=O)C(C)C(C)=O BGVBGAIWXAXBLP-UHFFFAOYSA-N 0.000 description 1
- FXIUOBFYAGRWJN-UHFFFAOYSA-N 3-ethylnonane-4,6-dione Chemical compound CCCC(=O)CC(=O)C(CC)CC FXIUOBFYAGRWJN-UHFFFAOYSA-N 0.000 description 1
- ZVXPYILZRIEUBN-UHFFFAOYSA-N 3-ethylundecane-4,6-dione Chemical compound CCCCCC(=O)CC(=O)C(CC)CC ZVXPYILZRIEUBN-UHFFFAOYSA-N 0.000 description 1
- GGQOYCFZZZEZMA-UHFFFAOYSA-N 4-ethyl-1-phenyloctane-1,3-dione Chemical compound CCCCC(CC)C(=O)CC(=O)C1=CC=CC=C1 GGQOYCFZZZEZMA-UHFFFAOYSA-N 0.000 description 1
- XVTWRQCEQFDSBK-UHFFFAOYSA-N 5-methyl-1-phenylhexane-1,3-dione Chemical compound CC(C)CC(=O)CC(=O)C1=CC=CC=C1 XVTWRQCEQFDSBK-UHFFFAOYSA-N 0.000 description 1
- NHKKBHCETRALIZ-UHFFFAOYSA-N 6-methyloctane-2,4-dione Chemical compound CCC(C)CC(=O)CC(C)=O NHKKBHCETRALIZ-UHFFFAOYSA-N 0.000 description 1
- KYNSBQPICQTCGU-UHFFFAOYSA-N Benzopyrane Chemical compound C1=CC=C2C=CCOC2=C1 KYNSBQPICQTCGU-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- JPIYZTWMUGTEHX-UHFFFAOYSA-N auramine O free base Chemical class C1=CC(N(C)C)=CC=C1C(=N)C1=CC=C(N(C)C)C=C1 JPIYZTWMUGTEHX-UHFFFAOYSA-N 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000006103 coloring component Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- WTVNFKVGGUWHQC-UHFFFAOYSA-N decane-2,4-dione Chemical compound CCCCCCC(=O)CC(C)=O WTVNFKVGGUWHQC-UHFFFAOYSA-N 0.000 description 1
- FMYKDKIKPGNXOW-UHFFFAOYSA-N decane-3,5,6,8-tetrone Chemical compound CCC(=O)CC(=O)C(=O)CC(=O)CC FMYKDKIKPGNXOW-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- ZONYXWQDUYMKFB-UHFFFAOYSA-N flavanone Chemical compound O1C2=CC=CC=C2C(=O)CC1C1=CC=CC=C1 ZONYXWQDUYMKFB-UHFFFAOYSA-N 0.000 description 1
- FWQHNLCNFPYBCA-UHFFFAOYSA-N fluoran Chemical class C12=CC=CC=C2OC2=CC=CC=C2C11OC(=O)C2=CC=CC=C21 FWQHNLCNFPYBCA-UHFFFAOYSA-N 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- CTHCTLCNUREAJV-UHFFFAOYSA-N heptane-2,4,6-trione Chemical compound CC(=O)CC(=O)CC(C)=O CTHCTLCNUREAJV-UHFFFAOYSA-N 0.000 description 1
- ILPNRWUGFSPGAA-UHFFFAOYSA-N heptane-2,4-dione Chemical compound CCCC(=O)CC(C)=O ILPNRWUGFSPGAA-UHFFFAOYSA-N 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- IVGFBEKIZGJTNX-UHFFFAOYSA-N hexadecane-2,4-dione Chemical compound CCCCCCCCCCCCC(=O)CC(C)=O IVGFBEKIZGJTNX-UHFFFAOYSA-N 0.000 description 1
- NDOGLIPWGGRQCO-UHFFFAOYSA-N hexane-2,4-dione Chemical compound CCC(=O)CC(C)=O NDOGLIPWGGRQCO-UHFFFAOYSA-N 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- XHEGBYNTQVVNCW-UHFFFAOYSA-N icosane-2,4-dione Chemical compound CCCCCCCCCCCCCCCCC(=O)CC(C)=O XHEGBYNTQVVNCW-UHFFFAOYSA-N 0.000 description 1
- 150000004715 keto acids Chemical class 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- SGGOJYZMTYGPCH-UHFFFAOYSA-L manganese(2+);naphthalene-2-carboxylate Chemical compound [Mn+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 SGGOJYZMTYGPCH-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- HKJHYQJXINHVSW-UHFFFAOYSA-N nonadecane-2,4-dione Chemical compound CCCCCCCCCCCCCCCC(=O)CC(C)=O HKJHYQJXINHVSW-UHFFFAOYSA-N 0.000 description 1
- IDDOXBGUYHBSKX-UHFFFAOYSA-N octadecane-2,4-dione Chemical compound CCCCCCCCCCCCCCC(=O)CC(C)=O IDDOXBGUYHBSKX-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- TVDDXVUEWIHEHC-UHFFFAOYSA-N octane-2,4,5,7-tetrone Chemical compound CC(=O)CC(=O)C(=O)CC(C)=O TVDDXVUEWIHEHC-UHFFFAOYSA-N 0.000 description 1
- KYWYXJJKXSANGZ-UHFFFAOYSA-N octane-2,4,6-trione Chemical compound CCC(=O)CC(=O)CC(C)=O KYWYXJJKXSANGZ-UHFFFAOYSA-N 0.000 description 1
- GJYXGIIWJFZCLN-UHFFFAOYSA-N octane-2,4-dione Chemical compound CCCCC(=O)CC(C)=O GJYXGIIWJFZCLN-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- HVINKLZTQUQDJO-UHFFFAOYSA-N pentadecane-2,4-dione Chemical compound CCCCCCCCCCCC(=O)CC(C)=O HVINKLZTQUQDJO-UHFFFAOYSA-N 0.000 description 1
- RIPZIAOLXVVULW-UHFFFAOYSA-N pentane-2,4-dione Chemical group CC(=O)CC(C)=O.CC(=O)CC(C)=O RIPZIAOLXVVULW-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001484 phenothiazinyl group Chemical class C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- HNUUPXWCBTYKDR-UHFFFAOYSA-N tetradecane-2,4-dione Chemical compound CCCCCCCCCCC(=O)CC(C)=O HNUUPXWCBTYKDR-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- AYNNSCRYTDRFCP-UHFFFAOYSA-N triazene Chemical compound NN=N AYNNSCRYTDRFCP-UHFFFAOYSA-N 0.000 description 1
- PZMFITAWSPYPDV-UHFFFAOYSA-N undecane-2,4-dione Chemical compound CCCCCCCC(=O)CC(C)=O PZMFITAWSPYPDV-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- B41M5/132—Chemical colour-forming components; Additives or binders therefor
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Color Printing (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56126576A JPS5845085A (ja) | 1981-08-14 | 1981-08-14 | 呈色組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56126576A JPS5845085A (ja) | 1981-08-14 | 1981-08-14 | 呈色組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5845085A JPS5845085A (ja) | 1983-03-16 |
| JPS645553B2 true JPS645553B2 (enrdf_load_stackoverflow) | 1989-01-31 |
Family
ID=14938581
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56126576A Granted JPS5845085A (ja) | 1981-08-14 | 1981-08-14 | 呈色組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5845085A (enrdf_load_stackoverflow) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3345675A4 (en) * | 2015-09-01 | 2019-04-24 | LG Chem, Ltd. | METHOD FOR PRODUCING A WATER TREATMENT MEMBRANE, WATER TREATMENT MEMBRANE MANUFACTURED THEREWITH AND WATER TREATMENT MODULE WITH THE WATER TREATMENT MEMBRANE |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6012956B2 (ja) * | 1978-08-05 | 1985-04-04 | 三菱製紙株式会社 | 感圧記録材料 |
-
1981
- 1981-08-14 JP JP56126576A patent/JPS5845085A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5845085A (ja) | 1983-03-16 |
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