JPH04177366A - Developer toner composition - Google Patents
Developer toner compositionInfo
- Publication number
- JPH04177366A JPH04177366A JP2307613A JP30761390A JPH04177366A JP H04177366 A JPH04177366 A JP H04177366A JP 2307613 A JP2307613 A JP 2307613A JP 30761390 A JP30761390 A JP 30761390A JP H04177366 A JPH04177366 A JP H04177366A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- color
- toner
- dye
- acid
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims description 17
- 239000002243 precursor Substances 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 8
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 3
- 229920001568 phenolic resin Polymers 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 36
- 239000000975 dye Substances 0.000 description 24
- 239000000843 powder Substances 0.000 description 13
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 12
- 239000003094 microcapsule Substances 0.000 description 9
- -1 p-dimethylaminophenyl Chemical group 0.000 description 9
- 239000001993 wax Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 7
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 6
- 229960004889 salicylic acid Drugs 0.000 description 6
- HCOFMIWUFBMIPV-UHFFFAOYSA-L zinc;2,4-ditert-butyl-6-carboxyphenolate Chemical compound [Zn+2].CC(C)(C)C1=CC(C(O)=O)=C([O-])C(C(C)(C)C)=C1.CC(C)(C)C1=CC(C(O)=O)=C([O-])C(C(C)(C)C)=C1 HCOFMIWUFBMIPV-UHFFFAOYSA-L 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229920003986 novolac Polymers 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
- 229920006243 acrylic copolymer Polymers 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 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
- 150000002148 esters Chemical class 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 1
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- YQTCQNIPQMJNTI-UHFFFAOYSA-N 2,2-dimethylpropan-1-one Chemical group CC(C)(C)[C]=O YQTCQNIPQMJNTI-UHFFFAOYSA-N 0.000 description 1
- BMOUJOURYKCKQF-UHFFFAOYSA-N 2-hydroxy-3-(1-phenylethyl)-5-(2-phenylpropan-2-yl)benzoic acid Chemical compound C=1C(C(C)(C)C=2C=CC=CC=2)=CC(C(O)=O)=C(O)C=1C(C)C1=CC=CC=C1 BMOUJOURYKCKQF-UHFFFAOYSA-N 0.000 description 1
- XOYXRDYXRJQLSN-UHFFFAOYSA-N 2-hydroxy-3-phenyl-5-(1-phenylethyl)benzoic acid Chemical compound C=1C(C(O)=O)=C(O)C(C=2C=CC=CC=2)=CC=1C(C)C1=CC=CC=C1 XOYXRDYXRJQLSN-UHFFFAOYSA-N 0.000 description 1
- YBXZFYBYIPONRP-UHFFFAOYSA-N 2-hydroxy-3-phenyl-5-(2-phenylpropan-2-yl)benzoic acid Chemical compound C=1C(C(O)=O)=C(O)C(C=2C=CC=CC=2)=CC=1C(C)(C)C1=CC=CC=C1 YBXZFYBYIPONRP-UHFFFAOYSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- BOWMELZGMRPCDJ-UHFFFAOYSA-N 3-cyclohexyl-2-hydroxy-5-(1-phenylethyl)benzoic acid Chemical compound C=1C(C2CCCCC2)=C(O)C(C(O)=O)=CC=1C(C)C1=CC=CC=C1 BOWMELZGMRPCDJ-UHFFFAOYSA-N 0.000 description 1
- ICBQZXYBJCJSJW-UHFFFAOYSA-N 3-cyclohexyl-2-hydroxy-5-phenylbenzoic acid Chemical compound OC=1C(C(=O)O)=CC(C=2C=CC=CC=2)=CC=1C1CCCCC1 ICBQZXYBJCJSJW-UHFFFAOYSA-N 0.000 description 1
- NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
- XURABDHWIADCPO-UHFFFAOYSA-N 4-prop-2-enylhepta-1,6-diene Chemical compound C=CCC(CC=C)CC=C XURABDHWIADCPO-UHFFFAOYSA-N 0.000 description 1
- XSHSRHGUKNUUQC-UHFFFAOYSA-N 5-benzyl-3-cyclohexyl-2-hydroxybenzoic acid Chemical compound C=1C(C2CCCCC2)=C(O)C(C(=O)O)=CC=1CC1=CC=CC=C1 XSHSRHGUKNUUQC-UHFFFAOYSA-N 0.000 description 1
- CTEDYBIVIFKMAZ-UHFFFAOYSA-N 5-cyclohexyl-2-hydroxy-3-(1-phenylethyl)benzoic acid Chemical compound C=1C(C2CCCCC2)=CC(C(O)=O)=C(O)C=1C(C)C1=CC=CC=C1 CTEDYBIVIFKMAZ-UHFFFAOYSA-N 0.000 description 1
- GZEPXNUXMPYSOQ-UHFFFAOYSA-N 5-cyclohexyl-2-hydroxybenzoic acid Chemical compound C1=C(O)C(C(=O)O)=CC(C2CCCCC2)=C1 GZEPXNUXMPYSOQ-UHFFFAOYSA-N 0.000 description 1
- RAHISFAHDJEGJO-UHFFFAOYSA-N 6-(dimethylamino)-3-[4-(dimethylamino)phenyl]-3-(2-methyl-1h-indol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC(N(C)C)=CC=C1C1(C=2C3=CC=CC=C3NC=2C)C2=CC=C(N(C)C)C=C2C(=O)O1 RAHISFAHDJEGJO-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000001263 FEMA 3042 Substances 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax 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
- 239000011230 binding agent Substances 0.000 description 1
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000011162 core material Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000009503 electrostatic coating Methods 0.000 description 1
- MFGZXPGKKJMZIY-UHFFFAOYSA-N ethyl 5-amino-1-(4-sulfamoylphenyl)pyrazole-4-carboxylate Chemical compound NC1=C(C(=O)OCC)C=NN1C1=CC=C(S(N)(=O)=O)C=C1 MFGZXPGKKJMZIY-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000012182 japan wax Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 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
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 229940075579 propyl gallate Drugs 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- 239000000473 propyl gallate Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- NBYLLBXLDOPANK-UHFFFAOYSA-M silver 2-carboxyphenolate hydrate Chemical compound C1=CC=C(C(=C1)C(=O)O)[O-].O.[Ag+] NBYLLBXLDOPANK-UHFFFAOYSA-M 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 239000011882 ultra-fine particle Substances 0.000 description 1
- JRBNKLYSGIHONX-UHFFFAOYSA-L zinc;1-carboxynaphthalen-2-olate Chemical compound [Zn+2].C1=CC=C2C(C(=O)O)=C([O-])C=CC2=C1.C1=CC=C2C(C(=O)O)=C([O-])C=CC2=C1 JRBNKLYSGIHONX-UHFFFAOYSA-L 0.000 description 1
- PJLLNWQQWBMNHM-UHFFFAOYSA-L zinc;2,3-ditert-butyl-6-carboxyphenolate Chemical compound [Zn+2].CC(C)(C)C1=CC=C(C(O)=O)C([O-])=C1C(C)(C)C.CC(C)(C)C1=CC=C(C(O)=O)C([O-])=C1C(C)(C)C PJLLNWQQWBMNHM-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Color Printing (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
[産業上の利用分野コ
本発明は、静電転写法に使用することのできる顕色剤ト
ナー組成物に関し、更に詳細には、圧力を加えることで
被記録媒体に定着を行なうことができ、染料または染料
前駆体と反応して十分な発色を得ることのできる顕色剤
トナー組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a developer toner composition that can be used in an electrostatic transfer method. The present invention relates to a developer toner composition that can be fixed and can react with dyes or dye precursors to obtain sufficient color development.
[従来の技術]
従来、顕色剤は水系溶媒中に超微粒子として分散されて
おり、バインダーや添加剤等の調整をされた上で抄紙さ
れた紙に塗布され、顕色剤シートという特殊紙として存
在していた。この顕色剤シートによる画像形成技術は、
特開昭58−88739号公報や特開昭59−3053
7号公報、更には特開昭59−137944号公報等に
開示されている。この画像形成技術とは、互いに隔離さ
れた二つまたはそれ以上の成分が、圧力または温度変化
などのような物理的外力によって隔離を解除され、互い
に反応する事によって光学的な変化、光の吸収領域、あ
るいは吸収強度の変化を起こし、外力に応じた記録がな
されるようなすべての機能を指すものである。[Conventional technology] Conventionally, a color developer is dispersed as ultrafine particles in an aqueous solvent, and after adjusting binders and additives, it is applied to the paper that is made into a special paper called a color developer sheet. existed as. The image forming technology using this color developer sheet is
JP-A-58-88739 and JP-A-59-3053
This method is disclosed in Japanese Patent Application Laid-Open No. 59-137944 and others. This image forming technology involves two or more components isolated from each other being released from isolation by physical external forces such as pressure or temperature changes, and reacting with each other, resulting in optical changes and absorption of light. It refers to all functions that cause changes in area or absorption intensity and are recorded in response to external forces.
例えば、光の照射により機械的破壊強度が変化するよう
なマイクロカプセルが任意の媒体上に担持しである感光
感圧記録媒体と顕色剤シートを重ね合わせ、圧力現像す
ることにより機械的破壊強度の異なったマイクロカプセ
ルの選択的清快を起こし、マイクロカプセルに含まれた
無色または僅かに着色した染料または、染料前駆体と反
応して染料を発色せしめうる物質、すなわち、染料受容
体ないしは顕色剤と反応して顕色剤シート上に顕像を形
成するような画像形成系である。この画像形成技術に準
じた形で、任意の記録媒体に画像を形成する手段として
、顕色剤を粉体にして静電的に任意の記録媒体に飛翔さ
せることで任意の記録媒体を基材とした顕色剤シートを
形成し、この顕色剤シート上にマイクロカプセルシート
と重ね合わせて圧力現像することによって、画像を形成
するという技術がある。また、この顕色剤粉体であると
ころの圧力定着性顕色剤トナーは、静電的に任意の記録
媒体上に付着した後、直接マイクロカプセルシートに接
触して、圧力現像装置で加圧されるため、任意の記録媒
体に加圧定着される性能をも持ち合わせ、圧力定着性顕
色剤トナー中に圧力定着成分を含んだ形となっている。For example, by overlapping a photosensitive pressure-sensitive recording medium, in which microcapsules whose mechanical breaking strength changes with light irradiation is supported on an arbitrary medium, and a color developer sheet, and performing pressure development, the mechanical breaking strength can be improved. A substance that selectively clears different microcapsules and reacts with colorless or slightly colored dyes or dye precursors contained in the microcapsules to develop a color, i.e., dye receptor or color developer. This is an image forming system that reacts with a developer to form a developed image on a developer sheet. In accordance with this image forming technology, as a means of forming an image on any recording medium, a color developer is made into powder and electrostatically flung onto any recording medium. There is a technique in which an image is formed by forming a color developer sheet, superimposing a microcapsule sheet on the color developer sheet, and performing pressure development. In addition, this pressure-fixing color developer toner, which is a color developer powder, is electrostatically adhered onto any recording medium, and then directly contacted with the microcapsule sheet and then pressurized with a pressure developing device. Therefore, it also has the ability to be pressure-fixed onto any recording medium, and contains a pressure-fixable component in the pressure-fixable color developer toner.
[発明が解決しようとする課題]
しかしながら、顕色剤を粉体としたとき顕色剤の本来の
特性から顕色剤トナーがべたつくという問題点があった
。これは顕色剤自身が粘着性を持っているためで、粉砕
による従来のトナーの製造法だけでは装置への付着がみ
られることや、顕色剤トナー粉体としての加圧定着性能
や流動性能か不十分であり、繰り返し使用に対して現像
性能や定着性能が不安定であり、トナー担持体やトナー
ケースへの癒着を起こし、保存中に凝集及びケーキ化し
保存安定性が悪かった。さらには、帯電性を悪くする原
因にもなり得た。そこで流動性能を改善しようとした場
合、以下のような別の問題が発生する。[Problems to be Solved by the Invention] However, when the developer is used as a powder, there is a problem that the developer toner becomes sticky due to the inherent characteristics of the developer. This is because the color developer itself is sticky, and if the conventional toner manufacturing method by pulverization is used alone, it may stick to the device, and the pressure fixing performance of the color developer toner powder may be affected. The performance was insufficient, the developing performance and fixing performance were unstable with repeated use, the toner adhered to the toner carrier and the toner case, agglomerated and caked during storage, and the storage stability was poor. Furthermore, it could also become a cause of poor charging properties. If an attempt is made to improve the flow performance, the following problems arise.
例えば、流動性のよい顕色剤は、発色性能に劣っていた
り、流動性はあるものの融点が高い為に、トナー製造工
程の一つ混練が融点の低い樹脂や顕色剤を混合しないと
できなかったり、トナー製造工程の一つ粉砕の時に微粉
の発生量が多く収率が悪かったり、耐候性に問題があっ
たりした。For example, a color developer with good fluidity may have poor coloring performance, or although it has fluidity, it has a high melting point, so kneading, which is one of the steps in the toner manufacturing process, cannot be performed without mixing a resin with a low melting point or a color developer. In some cases, the yield was poor due to a large amount of fine powder generated during pulverization, which is one of the toner manufacturing processes, and there were problems in weather resistance.
本発明は、上述した問題点を解決するためになされたも
のであり、被記録媒体である任意の記録媒体に対して加
圧による定着性が十分に得られると共に、トナーとして
の流動性が確保でき、しかも染料及び染料前駆体との発
色性能がよい顕色剤トナー組成物を提供することを目的
としている。The present invention has been made in order to solve the above-mentioned problems, and it is possible to obtain sufficient fixing properties by pressurization on any recording medium that is a recording medium, and to ensure fluidity as a toner. It is an object of the present invention to provide a color developer toner composition which can be used in combination with dyes and dye precursors and has good color development performance with dyes and dye precursors.
[課題を解決するための手段]
この目的を達成するために、本発明の顕色剤トナーは、
染料または染料前駆体と反応して発色させる染料受容体
である顕色剤が芳香族カルボン酸の多価金属塩とフェノ
ールノボラックから構成されている。[Means for Solving the Problems] In order to achieve this object, the developer toner of the present invention has the following features:
A color developer, which is a dye receptor that develops color by reacting with a dye or a dye precursor, is composed of a polyvalent metal salt of an aromatic carboxylic acid and a phenol novolac.
[作用コ
上記の構成を有する本発明によれば、染料受容体である
顕色剤として芳香族のカルボン酸とフェノールノボラッ
クを含有している(例えば、フェノールノボラック10
〜60wt%(重量パーセント)の中に芳香族カルボン
酸が30〜90wt%分散されている)。顕色能を持つ
物質として、2種類混合することでお互いの顕色効果を
補う発色能が得られるため、黒濃度が濃く、イエロー、
マゼンタ、シアンの各単色も明度、彩度の高い発色が得
られる。また、顕色剤トナーの製造上低い温度での溶融
混練が可能となる。[Function] According to the present invention having the above configuration, an aromatic carboxylic acid and a phenol novolac are contained as a color developer which is a dye receptor (for example, a phenol novolac 10
30 to 90 wt% of aromatic carboxylic acid is dispersed in ~60 wt% (weight percent). By mixing two types of substances that have color developing ability, you can obtain color developing ability that complements each other's color developing effect, so black density is deep, yellow,
Each single color of magenta and cyan can also produce colors with high brightness and saturation. Furthermore, it is possible to melt and knead the color developer toner at a low temperature in manufacturing the toner.
また、これら2種類の顕色剤成分と共に、被記録媒体へ
の圧力定着性を付与するために粘着剤やワックス等の軟
質物質を加熱混合する。顕色剤成分と圧力定着成分が一
つに取り込まれた塊を粉砕して、分級する事に依ってト
ナーとしての特性を備えた顕色剤トナーが作られる。In addition, a soft substance such as an adhesive or wax is heated and mixed with these two types of developer components in order to impart pressure fixing properties to the recording medium. By crushing and classifying a mass in which the color developer component and the pressure fixing component are combined, a color developer toner having the characteristics of a toner is produced.
[実施例]
以下、本発明を具体化した一実施例の構成要素について
説明する。[Example] Hereinafter, components of an example embodying the present invention will be described.
本実施例の顕色剤トナーが使われる画像形成系において
、顕色剤と反応する染料及び染料前駆体を含んだ光硬化
性のマイクロカプセルは、内包すれる光硬化性樹脂が、
光の照射量に応じて硬化する量が変化し、機械的破壊強
度が内包された光硬化性樹脂の硬化量に応じて変化する
。マイクロカプセルには、染料受容体である顕色剤との
反応で発色する発色媒体である染料及び染料前駆体が含
まれている。その例としては、クリスタルバイオレット
ラクトン、3−3−ビス(p−ジメチルアミノフェニル
)−フタリド、3− (p−ジメチルアミノフェニル)
−3−(2−メチルインドール−3−イル)−6−シメ
チルアミノフタライドのようなトリアリルメタンフタラ
イド系やメチレンブルーのベンゾイル、アニイゾイル、
ピバロイル等のアシル誘導体系:3−ジエチルアミノ−
7−クロロフルオラン、3−ジエチルアミノ−7−ジベ
ンジルアミノフルオラン、3−ジエチルアミノ−6−メ
チル−7−アニリノフルオラン、3−メチル−シクロへ
キシルアミノ−6−メチル−7−アニリノフルオラン、
3−エチル−p−トリルアミノ−6−メチル−7−アニ
リノフルオランのようなキサンチンフタライド系等のロ
イコ染料があり実用化されている。In the image forming system in which the developer toner of this example is used, the photocurable microcapsules containing the dye and dye precursor that react with the developer are
The amount of curing changes depending on the amount of light irradiation, and the mechanical breaking strength changes depending on the amount of curing of the included photocurable resin. The microcapsules contain a dye and a dye precursor, which are color-forming media that develop color by reaction with a developer, which is a dye receptor. Examples include crystal violet lactone, 3-3-bis(p-dimethylaminophenyl)-phthalide, 3-(p-dimethylaminophenyl)
-3-(2-methylindol-3-yl)-6-dimethylaminophthalide, triallylmethane phthalide, methylene blue benzoyl, anizoyl,
Acyl derivatives such as pivaloyl: 3-diethylamino-
7-chlorofluorane, 3-diethylamino-7-dibenzylaminofluorane, 3-diethylamino-6-methyl-7-anilinofluorane, 3-methyl-cyclohexylamino-6-methyl-7-anilinofluoran Oran,
Leuco dyes such as xanthine phthalide series such as 3-ethyl-p-tolylamino-6-methyl-7-anilinofluorane are available and have been put to practical use.
一方、マイクロカプセルに含有された染料前駆体が、圧
力によって潰れてマイクロカプセルから排出されたとき
、本実施例の顕色剤トナーの主成分である染料受容体の
顕色剤成分と反応して発色する。その顕色剤成分として
は、酸性白土、ベントナイト、アタパルガイド等の天然
粘土鉱物;タンニン酸、没食子酸、プロピル没食子酸エ
ステル等のような有機酸及びそのエステル;フェノール
樹脂、マレイン酸樹脂、フェノール−アセチレン樹脂、
少なくとも1個のヒドロキシ基を有するカルボン酸とホ
ルムアルデヒドとの縮重合物のような酸性ポリマー;サ
リチル酸亜鉛、サリチル酸銀、2−ヒドロキシナフトエ
酸亜鉛、3,5−ジ−t−ブチルサリチル酸亜鉛、3.
5−ジ(α−メチルベンジル)サリチル酸亜鉛のような
芳香族カルボン酸の金属塩;亜鉛、ニッケル等の多価金
属で変性した金属塩変性フェノール樹脂系化合物等かあ
げられる。On the other hand, when the dye precursor contained in the microcapsules is crushed by pressure and discharged from the microcapsules, it reacts with the developer component of the dye receiver, which is the main component of the developer toner of this example. Develops color. The color developer components include natural clay minerals such as acid clay, bentonite, and attapulgide; organic acids and their esters such as tannic acid, gallic acid, and propyl gallate; phenolic resin, maleic acid resin, and phenol-acetylene. resin,
Acidic polymers such as condensates of formaldehyde and carboxylic acids having at least one hydroxy group; zinc salicylate, silver salicylate, zinc 2-hydroxynaphthoate, zinc 3,5-di-t-butylsalicylate; 3.
Examples include metal salts of aromatic carboxylic acids such as zinc 5-di(α-methylbenzyl)salicylate; metal salt-modified phenolic resin compounds modified with polyvalent metals such as zinc and nickel.
中でも本発明においては、フェノールとホルムアルデヒ
ドの縮合物と、サリチル酸なとの芳香族カルボン酸の金
属塩との組合せにおける混合物は、顕色剤を顕色剤トナ
ーの成分とする上でたいへん有効である。フェノールと
ホルムアルデヒドの縮合物の例としてp−フェニルフェ
ノール、p−t−ブチルフェノール、p−オクチルフェ
ノール、ビスフェノールA等とホルムアルデヒドとの縮
合物があげられ、サリチル酸の金属塩の例として3゜5
−ジシクロへキシルサリチル酸、3−シクロへキシル−
5−フェニルサリチル酸、3−シクロへキシル−5−ベ
ンジルサリチル酸、3−シクロへキシル−5−(α−メ
チルベンジル)サリチル酸、3−(ジシクロヘキシル)
サリチル酸、3−(ジシクロヘキシル)−5−メチルサ
リチル酸、3−(ジシクロヘキシル)−5−エチルサリ
チル酸、3−(シンクロヘキシル)−5−t−ブチルサ
リチル酸、3−フェニル−5−(α−メチルベンジル)
サリチル酸、3−フェニル−5−(α、α−ジメチルベ
ンジル)サリチル酸、3−(α−メチルベンジル)−5
−シクロへキシルサリチル酸。Among these, in the present invention, a mixture of a condensate of phenol and formaldehyde in combination with a metal salt of an aromatic carboxylic acid such as salicylic acid is very effective in using a color developer as a component of a color developer toner. . Examples of condensates of phenol and formaldehyde include p-phenylphenol, p-t-butylphenol, p-octylphenol, bisphenol A, etc. and formaldehyde, and examples of metal salts of salicylic acid include 3.5
-dicyclohexylsalicylic acid, 3-cyclohexyl-
5-phenylsalicylic acid, 3-cyclohexyl-5-benzylsalicylic acid, 3-cyclohexyl-5-(α-methylbenzyl)salicylic acid, 3-(dicyclohexyl)
Salicylic acid, 3-(dicyclohexyl)-5-methylsalicylic acid, 3-(dicyclohexyl)-5-ethylsalicylic acid, 3-(synchlohexyl)-5-t-butylsalicylic acid, 3-phenyl-5-(α-methylbenzyl)
Salicylic acid, 3-phenyl-5-(α,α-dimethylbenzyl)salicylic acid, 3-(α-methylbenzyl)-5
- Cyclohexylsalicylic acid.
3.5−ジ(α−メチルベンジル)サリチル酸、3−(
α−メチルベンジル)−5−(α、α−ジメチルベンジ
ル)サリチル酸、3−(α、α−ジメチルベンジル)−
5−シクロへキシルサリチル酸、3−(α、α−ジメチ
ルベンジル)−5−(α−メチルベンジル)サリチル酸
、3.5−ジー(α、α−ジメチルベンジル)サリチル
酸等のマグネシウム、アルミニウム、カルシウム、マン
ガン、鉄、コバルト、ニッケル、銅、亜鉛、錫の塩が挙
げられる。3.5-di(α-methylbenzyl)salicylic acid, 3-(
α-methylbenzyl)-5-(α,α-dimethylbenzyl)salicylic acid, 3-(α,α-dimethylbenzyl)-
Magnesium, aluminum, calcium, such as 5-cyclohexylsalicylic acid, 3-(α,α-dimethylbenzyl)-5-(α-methylbenzyl)salicylic acid, 3.5-di(α,α-dimethylbenzyl)salicylic acid, These include salts of manganese, iron, cobalt, nickel, copper, zinc, and tin.
これら顕色剤の混合物を粉体化して静電的に任意の媒体
に塗布しようとする場合、顕色剤の粉体特性が影響して
、画像を形成するための記録媒体側に顕色剤が付着して
出力画像に抜けが生じ、確実な被記録媒体への定着がで
きないために染料前駆体である顕色剤に、被記録媒体側
だけに付着する圧力定着性能を付与する。被記録媒体へ
の顕色剤トナーの圧力定着性能は、その構成成分のから
みつき、接着性に関係し、顕色剤との相溶性、接着性の
よいワックス及び粘着剤を混合することにより、圧力定
着性能を高めることができる。例えば、粘着剤として知
られているエチレン−酢酸ビニル共重合体、ポリビニル
エーテル、塩化ビニル−酢酸ビニル共重合体、ポリ塩化
ビニル、ポリアクリル酸エステル、エチレン−エチルア
クリレート共重合体、ポリ酢酸ビニル、ポリビニルブチ
ラール、等があげられる。また、ワックスとしては、カ
ルナバワックス、キャンデリラワックス、ライスワック
ス、ラノリンワックス、ジャパンワックス、密ろうワッ
クス、パラフィンワックス、マイクロクリスタリンワッ
クス、モンタン酸ワックス、ハロゲン化パラフィンワッ
クス、アミドワックス、オシケライトや、ポリエチレン
、ポリプロピレンのようなポリオレフィン類等があげら
れる。When powdering a mixture of these color developers and electrostatically applying it to a desired medium, the powder characteristics of the color developer will affect the color developer's ability to form an image on the side of the recording medium. The dye adheres to the dye, causing defects in the output image and making it impossible to reliably fix it to the recording medium. Therefore, the color developer, which is a dye precursor, is given a pressure fixing ability that allows it to adhere only to the recording medium side. The pressure fixing performance of the color developer toner to the recording medium is related to the entanglement and adhesiveness of its constituent components. Fixing performance can be improved. For example, ethylene-vinyl acetate copolymer, polyvinyl ether, vinyl chloride-vinyl acetate copolymer, polyvinyl chloride, polyacrylic acid ester, ethylene-ethyl acrylate copolymer, polyvinyl acetate, which are known as adhesives, Examples include polyvinyl butyral. In addition, waxes include carnauba wax, candelilla wax, rice wax, lanolin wax, Japan wax, beeswax wax, paraffin wax, microcrystalline wax, montan acid wax, halogenated paraffin wax, amide wax, osikerite, polyethylene, Examples include polyolefins such as polypropylene.
また、必要に応じて第4級アンモニウム塩、アルキルア
ミド、有機錯体、ナフテン酸金属塩、脂肪酸金属塩等の
ような白色の荷電制御剤を混合すること、顕色剤と圧力
定着成分の混合物を芯物質として表面にコーティングを
施したり、球形化処理を行ない、顕色剤トナーの流動性
や帯電安定性を保持させることは本発明の顕色剤トナー
にとって有効な技術である。In addition, if necessary, a white charge control agent such as a quaternary ammonium salt, an alkyl amide, an organic complex, a naphthenic acid metal salt, a fatty acid metal salt, etc. may be mixed, and a mixture of a color developer and a pressure fixing component may be mixed. It is an effective technique for the developer toner of the present invention to maintain the fluidity and charging stability of the developer toner by applying a coating to the surface as a core material or performing a spheroidization treatment.
製造された顕色剤トナーを静電塗布装置に充填して、被
記録媒体である普通紙に静電転写をすると、トナーケー
ス内では流動性が良く、普通紙上に均一な塗布を施すこ
とができた。また、普通紙上に形成された画像の表面は
べたつきのない、原稿の黒色と差を感じることの無い黒
発色をもつ画像を形成することができた。When the manufactured color developer toner is filled into an electrostatic coating device and electrostatically transferred onto plain paper, which is a recording medium, it has good fluidity in the toner case and can be applied uniformly onto the plain paper. did it. Furthermore, the surface of the image formed on plain paper was not sticky, and an image with a black color that was indistinguishable from the black of the original could be formed.
[実験例1]
3.5−ジ−t−ブチルサリチル酸亜鉛・・・ 100
重量部
p−t−ブチルフェノールと
ホルムアルデヒドとの縮合物 ・・・ 60重量部エチ
レン−アクリル共重合体 ・・・ 30重量部ポリエ
チレンワックス ・・・ 20重量部潤滑剤
・・・ 5重量部上記顕色剤
トナー組成物において、p−t−ブチルフェノールとホ
ルムアルデヒドとの縮合物は、原料の時点で樹脂塊であ
り、3.5−ジ−t−ブチルサリチル酸亜鉛、ポリエチ
レンワックス、エチレン−アクリル共重合体、潤滑剤は
粉体である為、これらをヘンシェルミキサーによって乾
式でp−t−ブチルフェノールとホルムアルデヒドとの
縮合物を解砕しながら、粉体混合する。次にニーグーに
よって100℃で、融点の高い3,5−ジーt−ブチル
サリチル酸亜鉛の周りにp−t−ブチルフェノールとホ
ルムアルデヒドとの縮合物を主とした残りの成分をコー
ティングするような形で溶融混練し、常温で冷却固化す
る。引き出されて塊状にできた顕色剤トナー組成物は、
粗粉砕機で粉砕されて1.5mm以下の粒子にする。こ
れを気流式ジェットミルで微粉砕する。粉砕してできあ
がった粉体は、非常に細かい数μmの粉体から数百μm
の粉体まで含まれている。非常に細かい粉体と非常に粗
い粉体を気流式の分級機で分級してカットする。こうし
て平均粒径10μm前後の顕色剤トナーの粉体ができる
。この顕色剤組成物を使った顕色剤トナーを静電転写法
に依って被記録媒体に定着して、黒の発色をさせると黒
濃度1.86の発色が得られた。[Experiment Example 1] Zinc 3.5-di-t-butylsalicylate... 100
Part by weight Condensate of pt-butylphenol and formaldehyde 60 parts by weight Ethylene-acrylic copolymer 30 parts by weight Polyethylene wax 20 parts by weight Lubricant
... 5 parts by weight In the above color developer toner composition, the condensate of pt-butylphenol and formaldehyde is a resin lump at the time of raw material, and zinc 3,5-di-t-butylsalicylate, polyethylene Since the wax, ethylene-acrylic copolymer, and lubricant are powders, they are mixed into powders using a Henschel mixer while dryly crushing the condensate of pt-butylphenol and formaldehyde. Next, the remaining components, mainly consisting of a condensate of pt-butylphenol and formaldehyde, are melted at 100°C by a Niegoo so that the remaining components, mainly consisting of a condensate of pt-butylphenol and formaldehyde, are coated around zinc 3,5-di-t-butylsalicylate, which has a high melting point. Knead, cool and solidify at room temperature. The developer toner composition that has been drawn out and formed into a lump is
It is ground into particles of 1.5 mm or less using a coarse grinder. This is pulverized using an air jet mill. The resulting powder is extremely fine, ranging from a few micrometers in size to hundreds of micrometers in size.
Contains even powder. Very fine powder and very coarse powder are classified and cut using an air classifier. In this way, a developer toner powder having an average particle size of about 10 μm is produced. When a developer toner using this developer composition was fixed on a recording medium by an electrostatic transfer method to develop a black color, a color with a black density of 1.86 was obtained.
[実験例2]
p−t−ブチルフェノールとホルムアルデヒドとの縮合
物をp−フェニルフェノールとホルムアルデヒドとの縮
合物に変えて同様の操作で10μm前後の顕色剤トナー
を製造して静電転写法に依って被記録媒体に転写、定着
して、黒濃度を測定すると1.59の濃度であった。p
−フェニルフェノールとホルムアルデヒドとの縮合物を
混合するよりもp−t−ブチルフェノールとホルムアル
デヒドとの縮合物を3.5−ジ−t−ブチルサリチル酸
亜鉛に混合した方が濃い発色が得られる。[Experimental Example 2] A developer toner of around 10 μm was produced in the same manner by changing the condensate of p-t-butylphenol and formaldehyde to a condensate of p-phenylphenol and formaldehyde, and used in the electrostatic transfer method. Therefore, when the image was transferred and fixed onto a recording medium and the black density was measured, the density was 1.59. p
- A darker color can be obtained by mixing a condensate of pt-butylphenol and formaldehyde with zinc 3,5-di-t-butylsalicylate than by mixing a condensate of phenylphenol and formaldehyde.
[実験例3コ
実験例1の組成比を逆にした場合のp−t−ブチルフェ
ノールとホルムアルデヒドとの縮合物100重量部に対
して3.5−ジ−t−ブチルサリチル酸亜鉛60重量部
について、同様な操作で顕色剤トナーを製造し、静電転
写、感光感圧記録媒体との圧力現像を経て黒を発色させ
たときの濃度は、1.65であった。実験例1と組成比
を逆にするだけで濃度が下がる。3.5〜ジーt−ブチ
ルサリチル酸亜鉛の組成比を多くした方が黒濃度が高い
。[Experimental Example 3] Regarding 60 parts by weight of zinc 3.5-di-t-butylsalicylate for 100 parts by weight of the condensate of pt-butylphenol and formaldehyde when the composition ratio of Experimental Example 1 was reversed, A color developer toner was produced in the same manner, and the density when black was developed through electrostatic transfer and pressure development with a photosensitive and pressure sensitive recording medium was 1.65. The concentration can be reduced simply by reversing the composition ratio from Experimental Example 1. 3.5~The higher the composition ratio of zinc di-t-butylsalicylate, the higher the black density.
[実験例4]
実験例3のp−t−ブチルフェノールとホルムアルデヒ
ドとの縮合物をp−フェニルフェノールとホルムアルデ
ヒドとの縮合物に変えて同様な実験を行なうと、発色し
たときの濃度は1.42となった。組成比を変えた実験
においてもp−t−ブチルフェノールとホルムアルデヒ
ドとの縮合物より発色濃度が劣る。[Experimental Example 4] When a similar experiment was carried out by changing the condensate of p-t-butylphenol and formaldehyde in Experimental Example 3 to a condensate of p-phenylphenol and formaldehyde, the concentration when color was developed was 1.42. It became. Even in experiments with different composition ratios, the color density was inferior to that of the condensate of pt-butylphenol and formaldehyde.
以上4つの実験例をまとめたのが図面に示す表である。The above four experimental examples are summarized in the table shown in the drawing.
[発明の効果]
以上詳述したことから明らかなように、本発明によれば
、静電転写方式による良好な飛翔や転写を行なうことが
でき、しかも黒発色の十分な顕色剤トナー組成物が得ら
れるという産業上者しい効果を奏する。[Effects of the Invention] As is clear from the detailed description above, according to the present invention, a developer toner composition that can perform good flight and transfer by an electrostatic transfer method and has sufficient black color development can be obtained. This has the advantageous effect of being industrially superior.
図面は4つの実験例をまとめた表を表す図である。 The drawing is a diagram showing a table summarizing four experimental examples.
Claims (1)
容体である顕色剤と、圧力定着成分とを含有した顕色剤
トナー組成物において、 前記顕色剤が芳香族カルボン酸の多価金属塩とフェノー
ル−ホルムアルデヒド樹脂とから構成されていることを
特徴とする顕色剤トナー組成物。[Scope of Claims] 1. A developer toner composition containing a developer which is a dye receptor that develops color by reacting with a dye or a dye precursor, and a pressure fixing component, wherein the developer is aromatic. 1. A color developer toner composition comprising a polyvalent metal salt of a group carboxylic acid and a phenol-formaldehyde resin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2307613A JPH04177366A (en) | 1990-11-13 | 1990-11-13 | Developer toner composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2307613A JPH04177366A (en) | 1990-11-13 | 1990-11-13 | Developer toner composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04177366A true JPH04177366A (en) | 1992-06-24 |
Family
ID=17971143
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2307613A Pending JPH04177366A (en) | 1990-11-13 | 1990-11-13 | Developer toner composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04177366A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1057103C (en) * | 1997-12-31 | 2000-10-04 | 刘宗来 | Graft copolymer of modified phenolic resin and metallic carboxylate |
-
1990
- 1990-11-13 JP JP2307613A patent/JPH04177366A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1057103C (en) * | 1997-12-31 | 2000-10-04 | 刘宗来 | Graft copolymer of modified phenolic resin and metallic carboxylate |
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