JP6093237B2 - フッ素化ポリアミド酸を含有する中間転写部材 - Google Patents
フッ素化ポリアミド酸を含有する中間転写部材 Download PDFInfo
- Publication number
- JP6093237B2 JP6093237B2 JP2013099533A JP2013099533A JP6093237B2 JP 6093237 B2 JP6093237 B2 JP 6093237B2 JP 2013099533 A JP2013099533 A JP 2013099533A JP 2013099533 A JP2013099533 A JP 2013099533A JP 6093237 B2 JP6093237 B2 JP 6093237B2
- Authority
- JP
- Japan
- Prior art keywords
- polyamic acid
- intermediate transfer
- transfer member
- dianhydride
- oxydianiline
- 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 - Fee Related
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- 238000012546 transfer Methods 0.000 title claims description 116
- 229920005575 poly(amic acid) Polymers 0.000 title claims description 90
- 239000010702 perfluoropolyether Substances 0.000 claims description 44
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 claims description 43
- 239000000758 substrate Substances 0.000 claims description 39
- 239000000203 mixture Substances 0.000 claims description 33
- -1 polysiloxane Polymers 0.000 claims description 31
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 claims description 24
- 239000006229 carbon black Substances 0.000 claims description 18
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 claims description 18
- VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 13
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 claims description 12
- JVERADGGGBYHNP-UHFFFAOYSA-N 5-phenylbenzene-1,2,3,4-tetracarboxylic acid Chemical compound OC(=O)C1=C(C(O)=O)C(C(=O)O)=CC(C=2C=CC=CC=2)=C1C(O)=O JVERADGGGBYHNP-UHFFFAOYSA-N 0.000 claims description 12
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 12
- 229920001296 polysiloxane Polymers 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- VQVIHDPBMFABCQ-UHFFFAOYSA-N 5-(1,3-dioxo-2-benzofuran-5-carbonyl)-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(C=2C=C3C(=O)OC(=O)C3=CC=2)=O)=C1 VQVIHDPBMFABCQ-UHFFFAOYSA-N 0.000 claims description 7
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 229920000767 polyaniline Polymers 0.000 claims description 6
- 239000000470 constituent Substances 0.000 claims 1
- 239000010410 layer Substances 0.000 description 32
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 30
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- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
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- 230000000052 comparative effect Effects 0.000 description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
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- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 5
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- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical compound FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 5
- 239000008096 xylene Substances 0.000 description 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 4
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 150000004985 diamines Chemical class 0.000 description 4
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- 239000007787 solid Substances 0.000 description 4
- 241000721047 Danaus plexippus Species 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 229920006362 Teflon® Polymers 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
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- 125000006159 dianhydride group Chemical group 0.000 description 3
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 3
- 108091008695 photoreceptors Proteins 0.000 description 3
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 3
- UCQABCHSIIXVOY-UHFFFAOYSA-N 3-[4-[4-(3-aminophenoxy)phenyl]phenoxy]aniline Chemical group NC1=CC=CC(OC=2C=CC(=CC=2)C=2C=CC(OC=3C=C(N)C=CC=3)=CC=2)=C1 UCQABCHSIIXVOY-UHFFFAOYSA-N 0.000 description 2
- CCTFMNIEFHGTDU-UHFFFAOYSA-N 3-methoxypropyl acetate Chemical compound COCCCOC(C)=O CCTFMNIEFHGTDU-UHFFFAOYSA-N 0.000 description 2
- IWXCYYWDGDDPAC-UHFFFAOYSA-N 4-[(3,4-dicarboxyphenyl)methyl]phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1CC1=CC=C(C(O)=O)C(C(O)=O)=C1 IWXCYYWDGDDPAC-UHFFFAOYSA-N 0.000 description 2
- 238000004483 ATR-FTIR spectroscopy Methods 0.000 description 2
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
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- 239000004812 Fluorinated ethylene propylene Substances 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004962 Polyamide-imide Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229960001413 acetanilide Drugs 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
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- 229920001973 fluoroelastomer Polymers 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
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- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 description 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- LHENQXAPVKABON-UHFFFAOYSA-N 1-methoxypropan-1-ol Chemical compound CCC(O)OC LHENQXAPVKABON-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
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- CUDYYMUUJHLCGZ-UHFFFAOYSA-N 2-(2-methoxypropoxy)propan-1-ol Chemical compound COC(C)COC(C)CO CUDYYMUUJHLCGZ-UHFFFAOYSA-N 0.000 description 1
- MXPYJVUYLVNEBB-UHFFFAOYSA-N 2-[2-(2-carboxybenzoyl)oxycarbonylbenzoyl]oxycarbonylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OC(=O)C1=CC=CC=C1C(=O)OC(=O)C1=CC=CC=C1C(O)=O MXPYJVUYLVNEBB-UHFFFAOYSA-N 0.000 description 1
- SMDGQEQWSSYZKX-UHFFFAOYSA-N 3-(2,3-dicarboxyphenoxy)phthalic acid Chemical compound OC(=O)C1=CC=CC(OC=2C(=C(C(O)=O)C=CC=2)C(O)=O)=C1C(O)=O SMDGQEQWSSYZKX-UHFFFAOYSA-N 0.000 description 1
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- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
- LXJLFVRAWOOQDR-UHFFFAOYSA-N 3-(3-aminophenoxy)aniline Chemical compound NC1=CC=CC(OC=2C=C(N)C=CC=2)=C1 LXJLFVRAWOOQDR-UHFFFAOYSA-N 0.000 description 1
- ZBMISJGHVWNWTE-UHFFFAOYSA-N 3-(4-aminophenoxy)aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=CC(N)=C1 ZBMISJGHVWNWTE-UHFFFAOYSA-N 0.000 description 1
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- MFTFTIALAXXIMU-UHFFFAOYSA-N 3-[4-[2-[4-(3-aminophenoxy)phenyl]-1,1,1,3,3,3-hexafluoropropan-2-yl]phenoxy]aniline Chemical compound NC1=CC=CC(OC=2C=CC(=CC=2)C(C=2C=CC(OC=3C=C(N)C=CC=3)=CC=2)(C(F)(F)F)C(F)(F)F)=C1 MFTFTIALAXXIMU-UHFFFAOYSA-N 0.000 description 1
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- BEKFRNOZJSYWKZ-UHFFFAOYSA-N 4-[2-(4-aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl]aniline Chemical compound C1=CC(N)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(N)C=C1 BEKFRNOZJSYWKZ-UHFFFAOYSA-N 0.000 description 1
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- GQUSLIBGUTZKJZ-UHFFFAOYSA-N 4-[3-(3,4-dicarboxyphenoxy)phenoxy]phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1OC1=CC=CC(OC=2C=C(C(C(O)=O)=CC=2)C(O)=O)=C1 GQUSLIBGUTZKJZ-UHFFFAOYSA-N 0.000 description 1
- RQZSKJUAUIRPSB-UHFFFAOYSA-N 4-[4-[4-(3,4-dicarboxyphenoxy)phenoxy]phenoxy]phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1OC(C=C1)=CC=C1OC(C=C1)=CC=C1OC1=CC=C(C(O)=O)C(C(O)=O)=C1 RQZSKJUAUIRPSB-UHFFFAOYSA-N 0.000 description 1
- QQGYZOYWNCKGEK-UHFFFAOYSA-N 5-[(1,3-dioxo-2-benzofuran-5-yl)oxy]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(OC=2C=C3C(=O)OC(C3=CC=2)=O)=C1 QQGYZOYWNCKGEK-UHFFFAOYSA-N 0.000 description 1
- JCRLIUMXGPJBFK-UHFFFAOYSA-N 5-phenylbenzene-1,2,3,4-tetracarboxylic acid;dihydrate Chemical compound O.O.OC(=O)C1=C(C(O)=O)C(C(=O)O)=CC(C=2C=CC=CC=2)=C1C(O)=O JCRLIUMXGPJBFK-UHFFFAOYSA-N 0.000 description 1
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- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 238000001157 Fourier transform infrared spectrum Methods 0.000 description 1
- 101000903449 Homo sapiens Bestrophin-1 Proteins 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical class CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
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- 239000001825 Polyoxyethene (8) stearate Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 241000220010 Rhode Species 0.000 description 1
- 101001115232 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 40S ribosomal protein S22-A Proteins 0.000 description 1
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- 101000656770 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 40S ribosomal protein S24-A Proteins 0.000 description 1
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- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
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- 229920004747 ULTEM® 1000 Polymers 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- MRSWDOKCESOYBI-UHFFFAOYSA-N anthracene-2,3,6,7-tetracarboxylic acid Chemical compound OC(=O)C1=C(C(O)=O)C=C2C=C(C=C(C(C(=O)O)=C3)C(O)=O)C3=CC2=C1 MRSWDOKCESOYBI-UHFFFAOYSA-N 0.000 description 1
- GCAIEATUVJFSMC-UHFFFAOYSA-N benzene-1,2,3,4-tetracarboxylic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1C(O)=O GCAIEATUVJFSMC-UHFFFAOYSA-N 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical group C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- BBRLKRNNIMVXOD-UHFFFAOYSA-N bis[4-(3-aminophenoxy)phenyl]methanone Chemical compound NC1=CC=CC(OC=2C=CC(=CC=2)C(=O)C=2C=CC(OC=3C=C(N)C=CC=3)=CC=2)=C1 BBRLKRNNIMVXOD-UHFFFAOYSA-N 0.000 description 1
- LSDYQEILXDCDTR-UHFFFAOYSA-N bis[4-(4-aminophenoxy)phenyl]methanone Chemical compound C1=CC(N)=CC=C1OC1=CC=C(C(=O)C=2C=CC(OC=3C=CC(N)=CC=3)=CC=2)C=C1 LSDYQEILXDCDTR-UHFFFAOYSA-N 0.000 description 1
- WKDNYTOXBCRNPV-UHFFFAOYSA-N bpda Chemical compound C1=C2C(=O)OC(=O)C2=CC(C=2C=C3C(=O)OC(C3=CC=2)=O)=C1 WKDNYTOXBCRNPV-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
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- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- STZIXLPVKZUAMV-UHFFFAOYSA-N cyclopentane-1,1,2,2-tetracarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CCCC1(C(O)=O)C(O)=O STZIXLPVKZUAMV-UHFFFAOYSA-N 0.000 description 1
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- 150000002148 esters Chemical class 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
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- 125000001153 fluoro group Chemical group F* 0.000 description 1
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- 238000000227 grinding Methods 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- DOBFTMLCEYUAQC-UHFFFAOYSA-N naphthalene-2,3,6,7-tetracarboxylic acid Chemical compound OC(=O)C1=C(C(O)=O)C=C2C=C(C(O)=O)C(C(=O)O)=CC2=C1 DOBFTMLCEYUAQC-UHFFFAOYSA-N 0.000 description 1
- YTVNOVQHSGMMOV-UHFFFAOYSA-N naphthalenetetracarboxylic dianhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=C2C(=O)OC(=O)C1=C32 YTVNOVQHSGMMOV-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- CLYVDMAATCIVBF-UHFFFAOYSA-N pigment red 224 Chemical compound C=12C3=CC=C(C(OC4=O)=O)C2=C4C=CC=1C1=CC=C2C(=O)OC(=O)C4=CC=C3C1=C42 CLYVDMAATCIVBF-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920003223 poly(pyromellitimide-1,4-diphenyl ether) Polymers 0.000 description 1
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- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000000930 thermomechanical effect Effects 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
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- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
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- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
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- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
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Description
フッ素化ペルフルオロポリエーテル(PFPE)との混合のために選択されるポリアミド酸の例としては、ピロメリト酸二無水物/4,4’−オキシジアニリンのポリアミド酸、ピロメリト酸二無水物/フェニレンジアミンのポリアミド酸、ビフェニルテトラカルボン酸二無水物/4,4’−オキシジアニリンのポリアミド酸、ビフェニルテトラカルボン酸二水物/フェニレンジアミンのポリアミド酸、ベンゾフェノンテトラカルボン酸二水物/4,4’−オキシジアニリンのポリアミド酸、ベンゾフェノンテトラカルボン酸二水物/4,4’−オキシジアニリン/フェニレンジアミンのポリアミド酸、およびこれらに類するもの、ならびにそれらの混合物が挙げられる。
選択される官能化ペルフルオロポリエーテルの例は、カルボン酸官能化ペルフルオロポリエーテル(HOOC−PFPE−COOH)であり、その例は、
中間転写部材は一般的に、ポリシロキサンポリマーを含むこともできる。本明細書において開示される中間転写部材混合物のために選択されるポリシロキサンポリマーの例としては、BYK ChemicalからBYK(登録商標)333、BYK(登録商標)330(メトキシプロピルアセタートにおける約51重量%)、およびBYK(登録商標)344(80:20比のキシレン:イソブタノールにおける約52.3重量%)として市販されているポリエーテル修飾したポリジメチルシロキサン;BYK(登録商標)−SILCLEAN3710およびBYK(登録商標)3720(メトキシプロパノールにおける約25重量%);BYK ChemicalからBYK(登録商標)310(キシレンにおける約25重量%)およびBYK(登録商標)370(75:11:7:7比のキシレン:アルキルベンゼン:シクロヘキサノン:モノフェニルグリコールにおける約25重量%)として市販されているポリエステル修飾したポリジメチルシロキサン;BYK ChemicalからBYK(登録商標)−SILCLEAN3700(メトキシプロピルアセタートにおける約25重量%)として市販されているポリアクリラート修飾したポリジメチルシロキサン;BYK ChemicalからBYK(登録商標)375(ジ−プロピレングリコールモノメチルエーテルにおける約25重量%)として市販されているポリエステルポリエーテル修飾したポリジメチルシロキサン;およびこれらに類するもの、ならびにそれらの混合物など、公知の好適なポリシロキサンが挙げられる。
任意に、中間転写部材は、例えば中間転写部材の導電性を変更および調整するために、1種類以上の填材を含有してもよい。中間転写部材が単層構造である場合、導電性填材は、本明細書に開示されるフッ素化ポリアミド酸含有混合物中に含まれることができる。しかしながら、中間転写部材が多層構造である場合、導電性填材は、支持基材中、該支持基材上を被覆するポリマー混合物層中、ならびに支持基材およびポリマー混合物層の両方の中など、該部材の1つ以上の層の中に含まれることができる。
所望の場合、任意の放出層は、本明細書に説明されるフッ素化ポリアミド酸層混合物の上など、中間転写部材中に含むことができる。該放出層は、追加的なトナー洗浄を提供することを、および光導電体から中間転写部材へのさらなる顕色した像の転写効率を支援するために含んでもよい。
生成したフッ素化ポリアミド酸および導電性填材成分を含む、本明細書に説明される中間転写部材混合物は、何らかの好適な方法によって中間転写部材へと製剤化することができる。例えば、公知の粉砕過程を使用して、中間転写部材混合物の均一な分散物を得、約125℃〜約400℃、約200℃〜約350℃、または約160℃〜約290℃で、例えば約30分間〜約120分間、または約45分間〜約100分間の好適な時間加熱および硬化させて、カルボン酸官能化ペルフルオロポリエーテルのカルボン酸基とポリアミド酸の間の反応を完了させ、次に、ステンレス鋼基材もしくはそれに類するものなど個々の金属基材上を、公知の画線棒(draw bar)塗布方法もしくは流し塗り方法を使用して被覆することができる。結果として生じる個々のフィルムまたは複数のフィルムは、該フィルムを190℃で30分間、250℃で30分間、および290℃で60分間加熱および硬化させることによって、あるいは中間転写部材混合物を約100℃〜約400℃、約75℃〜約320℃、または約160℃〜約320℃に、約20〜約180分間、約40〜約120分間、または約30〜約60分間などの好適な時間、該基材上に残存しながら加熱することによって一般的に硬化させることによるなど、高温で乾燥させることができる。乾燥および室温(約23℃〜約25℃)への冷却後、該フィルムを該鋼基材から自己放出し、すなわち、該フィルムは何ら外部の支援を用いることなく放出する。結果として生じる中間転写フィルム製品は、例えば約15〜約150ミクロン、約20〜約100ミクロン、または約25〜約80ミクロンの厚さを有することができる。
所望の場合、支持基材を、生成したフッ素化ポリアミド酸含有層の真下など、中間転写部材の中に含むことができる。任意の支持基材は、高い剛性または強度を中間転写部材に提供するために含むことができる。
約16重量固体のN−メチル−2−ピロリドン(NMP)における、初期混合供給量を基にした15:85比のEvonik−DeGussa社から得た特殊カーボンブラック4とIndustrial Summit Technology社(米国ニュージャージー州パーリン)から得ることのできるピロメリト酸二無水物/4,4−オキシジアニリンのポリアミド酸(Pyre−M.L.RC5083(メチル−2−ピロリドンとN,N−ジメチルアセトアミドの溶媒混合物(NMP:DMAc比15:85)における約18〜約19重量%))の混合物を撹拌することによって、被膜組成物を調製した。得られた中間転写部材分散液で厚さ0.5mmのステンレス鋼基材を被覆した後、該混合物を125℃で30分間、190℃で30分間、および320℃で60分間加熱することによって硬化させた。示された比における先の成分から構成された、結果と生じる中間転写部材フィルムは、ステンレス基材から自己放出せず、むしろこの基材に接着した。水中で3分間浸漬した後、得られた中間転写部材フィルムは最終的に、この基材から自己放出した。
ボールミルを使用して撹拌しながら、初期混合物供給量を基にした70:30の重量比で、Industrial Summit Technology社(米国ニュージャージー州パーリン)からPyre−M.L.RC5083の商品名で市販されているピロメリト酸二無水物/4,4−オキシジアニリンのポリアミド酸と、カルボン酸官能化PFPEであるSolvay Solexis製のFLUOROLINK(登録商標)C10との反応から生成されるPFPE修飾したポリアミド酸被膜組成物、および約16重量固体のN−メチル−2−ピロリドンにおけるEvonik−Degussa社から得られる特殊カーボンブラック4を混合することによって調製した。PFPE修飾したポリアミド酸とカーボンブラックとの重量比は約85:15であった。結果として生じる混合物を次に、55℃に4時間加熱した後、約25℃に冷却して、PFPE修飾したポリアミド酸/カーボンブラック被膜を得た。
中間転写部材を、実施例1の過程を反復することによって調製するが、例外は、ポリアミド酸のために、ビフェニルテトラカルボン酸二無水物/4,4’−オキシジアニリンのポリアミド酸(UBE America社から得たU−VARNISH A)、ビフェニルテトラカルボン酸二無水物/フェニレンジアミンのポリアミド酸(HD MicroSystems社から得たPI−2610)、ベンゾフェノンテトラカルボン酸二無水物/4,4’−オキシジアニリンのポリアミド酸(Unitech社から得たRP50)、またはベンゾフェノンテトラカルボン酸二無水物/4,4’−オキシジアニリン/フェニレンジアミンのポリアミド酸(HD MicroSystems社から得たPI−2525)が選択されることである。
高抵抗率メーターを使用して測定された先の実施例1の抵抗率は、約6.4×1010Ω/平方であった。
Claims (18)
- 前記中間転写部材は、疎油性である、請求項1に記載の中間転写部材。
- 前記ポリアミド酸は、ピロメリト酸二無水物/4,4’−オキシジアニリンのポリアミド酸、およびビフェニルテトラカルボン酸二無水物/4,4’−オキシジアニリンのポリアミド酸からなる群より選択される、請求項1に記載の中間転写部材。
- 前記該官能化ペルフルオロポリエーテルは、下記式により表され、
前記ポリアミド酸は、ピロメリト酸二無水物/4,4’−オキシジアニリンのポリアミド酸、ピロメリト酸二無水物/フェニレンジアミンのポリアミド酸、ビフェニルテトラカルボン酸二無水物/4,4’−オキシジアニリンのポリアミド酸、ビフェニルテトラカルボン酸二無水物/フェニレンジアミンのポリアミド酸、ベンゾフェノンテトラカルボン酸二無水物/4,4’−オキシジアニリンのポリアミド酸、ベンゾフェノンテトラカルボン酸二無水物/4,4’−オキシジアニリン/フェニレンジアミンのポリアミド酸、およびこれらの混合物からなる群から選択される、請求項1に記載の中間転写部材。 - 前記ポリアミド酸は、ピロメリト酸二無水物/4,4’−オキシジアニリンのポリアミド酸であり、
前記該官能化ペルフルオロポリエーテルについて、nは10〜60であり、mは10〜60であり、n/mの比は0.5〜2である、請求項1に記載の中間転写部材。 - 前記ポリアミド酸と前記官能化ペルフルオロポリエーテルの比は、90:10、80:20、70:30、または50;50である、請求項1に記載の中間転写部材。
- 前記ポリアミド酸と前記官能化ペルフルオロポリエーテルの比は、70:30である、請求項1に記載の中間転写部材。
- 前記ポリアミド酸は、約50〜約95重量%の量から選択され、
前記官能化ペルフルオロポリエーテルは、約5〜約50重量%の量から選択され、
これらの合計が約100%である、請求項1に記載の中間転写部材。 - カルボン酸官能化ペルフルオロポリエーテルのカルボン酸基は、加熱によって前記ポリアミド酸と反応する、請求項1に記載の中間転写部材。
- 前記カーボンブラックは、前記中間転写部材の構成成分の合計が100%として、約3〜約40重量%の量で存在する、請求項1に記載の中間転写部材。
- 前記中間転写部材は、約109〜約1013Ω/平方の抵抗率を有する、請求項1に記載の中間転写部材。
- 前記中間転写部材は、フィルムの形態であり、かつ金属基材から自己放出し、約50〜約120°のヘキサデカン接触角を有する、請求項1に記載の中間転写部材。
- 前記中間転写部材は、約55〜約90°のヘキサデカン接触角を有する、請求項1に記載の中間転写部材。
- 前記該官能化ペルフルオロポリエーテルについて、nは10〜60であり、mは10〜60であり、n/mの比は0.5〜2である、請求項14に記載の中間転写部材。
- 前記ポリアミド酸は、ピロメリト酸二無水物/4,4’−オキシジアニリンのポリアミド酸、ピロメリト酸二無水物/フェニレンジアミンのポリアミド酸、ビフェニルテトラカルボン酸二無水物/4,4’−オキシジアニリンのポリアミド酸、ビフェニルテトラカルボン酸二無水物/フェニレンジアミンのポリアミド酸、ベンゾフェノンテトラカルボン酸二無水物/4,4’−オキシジアニリンのポリアミド酸、およびベンゾフェノンテトラカルボン酸二無水物/4,4’−オキシジアニリン/フェニレンジアミンのポリアミド酸からなる群から選択される、請求項14に記載の中間転写部材。
- フッ素化ポリアミド酸と、ポリシロキサンと、カーボンブラックとを含む層を備え、前記フッ素化ポリアミド酸は、ポリアミド酸と官能化ペルフルオロポリエーテルとの反応によって生成され、
前記ポリアミド酸は、ピロメリト酸二無水物/4,4’−オキシジアニリンのポリアミド酸、およびビフェニルテトラカルボン酸二無水物/4,4’−オキシジアニリンのポリアミド酸からなる群より選択され、
前記該官能化ペルフルオロポリエーテルは、カルボン酸終端化ペルフルオロポリエーテルであり、前記カルボン酸官能化ペルフルオロポリエーテルのカルボン酸基は、前記ポリアミド酸と反応し、
前記中間転写部材は、約50〜約90°のヘキサデカン接触角を有する疎油性であり、
前記該官能化ペルフルオロポリエーテルは、下記式により表され、
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JP6738124B2 (ja) * | 2014-12-26 | 2020-08-12 | ヒューレット−パッカード デベロップメント カンパニー エル.ピー.Hewlett‐Packard Development Company, L.P. | 転写搬送装置及び画像形成装置 |
US10125218B2 (en) * | 2016-07-26 | 2018-11-13 | Xerox Corporation | Intermediate transfer members |
US11725079B2 (en) | 2020-07-20 | 2023-08-15 | The Boeing Company | Polyimide compositions and articles incorporating the same |
US11845834B2 (en) | 2020-09-23 | 2023-12-19 | The Boeing Company | Polyamide compositions and articles incorporating the same |
US11697709B2 (en) * | 2020-10-07 | 2023-07-11 | The Boeing Company | Poly(arylene ether) compositions and articles incorporating the same |
US20220206421A1 (en) * | 2020-12-25 | 2022-06-30 | Canon Kabushiki Kaisha | Fixing rotating member, fixing apparatus, electrophotographic image forming apparatus, and method for producing fixing rotating member |
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US5978639A (en) | 1997-05-02 | 1999-11-02 | Bridgestone Corporation | Intermediate transfer member and intermediate transfer device |
US6397034B1 (en) | 1997-08-29 | 2002-05-28 | Xerox Corporation | Fluorinated carbon filled polyimide intermediate transfer components |
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