JP2002527564A - ポリマー被覆の炭素生成物及びその他の顔料並びに水性媒質重合法又は溶媒コーティング法によるそれらの製造法 - Google Patents
ポリマー被覆の炭素生成物及びその他の顔料並びに水性媒質重合法又は溶媒コーティング法によるそれらの製造法Info
- Publication number
- JP2002527564A JP2002527564A JP2000575948A JP2000575948A JP2002527564A JP 2002527564 A JP2002527564 A JP 2002527564A JP 2000575948 A JP2000575948 A JP 2000575948A JP 2000575948 A JP2000575948 A JP 2000575948A JP 2002527564 A JP2002527564 A JP 2002527564A
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- carbon product
- modified carbon
- product
- group
- 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.)
- Withdrawn
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 295
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 118
- 229910052799 carbon Inorganic materials 0.000 title claims abstract description 92
- 238000000576 coating method Methods 0.000 title claims abstract description 86
- 238000006116 polymerization reaction Methods 0.000 title claims abstract description 66
- 239000011248 coating agent Substances 0.000 title claims description 77
- 239000002904 solvent Substances 0.000 title claims description 49
- 239000012736 aqueous medium Substances 0.000 title claims description 11
- 238000002360 preparation method Methods 0.000 title abstract description 5
- 239000000049 pigment Substances 0.000 title description 16
- 150000001721 carbon Chemical class 0.000 claims abstract description 243
- 238000000034 method Methods 0.000 claims abstract description 110
- 125000000962 organic group Chemical group 0.000 claims abstract description 108
- 230000008569 process Effects 0.000 claims abstract description 11
- 239000003960 organic solvent Substances 0.000 claims abstract description 9
- 239000006229 carbon black Substances 0.000 claims description 105
- 239000000178 monomer Substances 0.000 claims description 81
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 63
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 48
- -1 sulfophenyl group Chemical group 0.000 claims description 43
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 39
- 239000000203 mixture Substances 0.000 claims description 38
- 150000003839 salts Chemical class 0.000 claims description 37
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 31
- 239000003999 initiator Substances 0.000 claims description 26
- 239000002609 medium Substances 0.000 claims description 24
- 125000003118 aryl group Chemical group 0.000 claims description 22
- 239000006185 dispersion Substances 0.000 claims description 20
- 239000011159 matrix material Substances 0.000 claims description 20
- 239000004594 Masterbatch (MB) Substances 0.000 claims description 17
- 239000004793 Polystyrene Substances 0.000 claims description 16
- 238000001704 evaporation Methods 0.000 claims description 15
- 238000010526 radical polymerization reaction Methods 0.000 claims description 15
- 238000002156 mixing Methods 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 11
- 125000001624 naphthyl group Chemical group 0.000 claims description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 9
- 229920001577 copolymer Polymers 0.000 claims description 9
- 230000008020 evaporation Effects 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 229920000098 polyolefin Polymers 0.000 claims description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- 230000015572 biosynthetic process Effects 0.000 claims description 7
- 125000003010 ionic group Chemical group 0.000 claims description 7
- 239000004417 polycarbonate Substances 0.000 claims description 7
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 6
- 238000001914 filtration Methods 0.000 claims description 6
- 229920002223 polystyrene Polymers 0.000 claims description 6
- 229920005989 resin Polymers 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 6
- 229910052710 silicon Inorganic materials 0.000 claims description 6
- 239000010703 silicon Substances 0.000 claims description 6
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 239000004917 carbon fiber Substances 0.000 claims description 5
- 229910021397 glassy carbon Inorganic materials 0.000 claims description 5
- 229910002804 graphite Inorganic materials 0.000 claims description 5
- 239000010439 graphite Substances 0.000 claims description 5
- 238000011065 in-situ storage Methods 0.000 claims description 5
- 239000010410 layer Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 5
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 5
- 229920000515 polycarbonate Polymers 0.000 claims description 5
- 238000000926 separation method Methods 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- 239000004677 Nylon Substances 0.000 claims description 4
- 239000004952 Polyamide Substances 0.000 claims description 4
- 239000004642 Polyimide Substances 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 4
- 238000004108 freeze drying Methods 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 229920001778 nylon Polymers 0.000 claims description 4
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 4
- 229920002239 polyacrylonitrile Polymers 0.000 claims description 4
- 229920002647 polyamide Polymers 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims description 4
- 229920001721 polyimide Polymers 0.000 claims description 4
- 239000004814 polyurethane Substances 0.000 claims description 4
- 229920002635 polyurethane Polymers 0.000 claims description 4
- 239000004800 polyvinyl chloride Substances 0.000 claims description 4
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 4
- 238000001556 precipitation Methods 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 238000001694 spray drying Methods 0.000 claims description 4
- 125000000626 sulfinic acid group Chemical group 0.000 claims description 4
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- 238000012546 transfer Methods 0.000 claims description 4
- 229920001567 vinyl ester resin Polymers 0.000 claims description 4
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 3
- 229920000106 Liquid crystal polymer Polymers 0.000 claims description 3
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 claims description 3
- 229920000877 Melamine resin Polymers 0.000 claims description 3
- 229920002292 Nylon 6 Polymers 0.000 claims description 3
- 239000004962 Polyamide-imide Substances 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 229920002367 Polyisobutene Polymers 0.000 claims description 3
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 3
- 229920000180 alkyd Polymers 0.000 claims description 3
- 239000003153 chemical reaction reagent Substances 0.000 claims description 3
- 229920002313 fluoropolymer Polymers 0.000 claims description 3
- 239000004811 fluoropolymer Substances 0.000 claims description 3
- 229920000554 ionomer Polymers 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- 239000004816 latex Substances 0.000 claims description 3
- 229920000126 latex Polymers 0.000 claims description 3
- 150000002978 peroxides Chemical group 0.000 claims description 3
- 229920000058 polyacrylate Polymers 0.000 claims description 3
- 229920002312 polyamide-imide Polymers 0.000 claims description 3
- 229920000647 polyepoxide Polymers 0.000 claims description 3
- 229920000570 polyether Polymers 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 229920001195 polyisoprene Polymers 0.000 claims description 3
- 229920006324 polyoxymethylene Polymers 0.000 claims description 3
- 229920006380 polyphenylene oxide Polymers 0.000 claims description 3
- 229920005573 silicon-containing polymer Polymers 0.000 claims description 3
- 229910052709 silver Inorganic materials 0.000 claims description 3
- 239000004332 silver Substances 0.000 claims description 3
- 238000010557 suspension polymerization reaction Methods 0.000 claims description 3
- 229920002725 thermoplastic elastomer Polymers 0.000 claims description 3
- 229920006305 unsaturated polyester Polymers 0.000 claims description 3
- 238000005119 centrifugation Methods 0.000 claims description 2
- 238000007156 chain growth polymerization reaction Methods 0.000 claims description 2
- 229920001568 phenolic resin Polymers 0.000 claims description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims 3
- 125000001453 quaternary ammonium group Chemical group 0.000 claims 3
- 239000004640 Melamine resin Substances 0.000 claims 2
- 239000003822 epoxy resin Substances 0.000 claims 2
- 239000005518 polymer electrolyte Substances 0.000 claims 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 229920002396 Polyurea Polymers 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 238000000151 deposition Methods 0.000 claims 1
- 238000005189 flocculation Methods 0.000 claims 1
- 230000016615 flocculation Effects 0.000 claims 1
- 238000012643 polycondensation polymerization Methods 0.000 claims 1
- 239000002356 single layer Substances 0.000 claims 1
- 238000007155 step growth polymerization reaction Methods 0.000 claims 1
- 239000000047 product Substances 0.000 description 218
- 238000006243 chemical reaction Methods 0.000 description 51
- 150000001875 compounds Chemical class 0.000 description 33
- 239000000243 solution Substances 0.000 description 29
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 26
- 239000003505 polymerization initiator Substances 0.000 description 22
- 229920000638 styrene acrylonitrile Polymers 0.000 description 19
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000012954 diazonium Substances 0.000 description 18
- 150000001989 diazonium salts Chemical class 0.000 description 18
- 229920001897 terpolymer Polymers 0.000 description 18
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 17
- 239000000463 material Substances 0.000 description 16
- 239000002245 particle Substances 0.000 description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 15
- 238000012937 correction Methods 0.000 description 15
- 238000002474 experimental method Methods 0.000 description 15
- 238000001030 gas--liquid chromatography Methods 0.000 description 14
- 238000000113 differential scanning calorimetry Methods 0.000 description 13
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 13
- 238000013341 scale-up Methods 0.000 description 13
- 239000011734 sodium Substances 0.000 description 13
- 239000002253 acid Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 229910052757 nitrogen Chemical group 0.000 description 9
- 238000009864 tensile test Methods 0.000 description 9
- 230000008859 change Effects 0.000 description 8
- 125000000524 functional group Chemical group 0.000 description 8
- 239000012299 nitrogen atmosphere Substances 0.000 description 8
- 241000894007 species Species 0.000 description 8
- 238000011282 treatment Methods 0.000 description 8
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 7
- 150000001450 anions Chemical class 0.000 description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- 238000013329 compounding Methods 0.000 description 6
- 238000009863 impact test Methods 0.000 description 6
- 230000035484 reaction time Effects 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000000010 aprotic solvent Substances 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 229920001971 elastomer Polymers 0.000 description 5
- 238000010556 emulsion polymerization method Methods 0.000 description 5
- 238000000605 extraction Methods 0.000 description 5
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 5
- 238000001746 injection moulding Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000012429 reaction media Substances 0.000 description 5
- 230000002787 reinforcement Effects 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 125000001072 heteroaryl group Chemical group 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 230000002572 peristaltic effect Effects 0.000 description 4
- 238000013001 point bending Methods 0.000 description 4
- 150000003141 primary amines Chemical class 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- 239000003586 protic polar solvent Substances 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 4
- 238000002411 thermogravimetry Methods 0.000 description 4
- 230000004580 weight loss Effects 0.000 description 4
- VFXXTYGQYWRHJP-UHFFFAOYSA-N 4,4'-azobis(4-cyanopentanoic acid) Chemical compound OC(=O)CCC(C)(C#N)N=NC(C)(CCC(O)=O)C#N VFXXTYGQYWRHJP-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 238000004566 IR spectroscopy Methods 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 3
- 125000000732 arylene group Chemical group 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 230000000977 initiatory effect Effects 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 239000003607 modifier Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 235000005985 organic acids Nutrition 0.000 description 3
- 125000004076 pyridyl group Chemical group 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- ILWJAOPQHOZXAN-UHFFFAOYSA-N 1,3-dithianyl Chemical group [CH]1SCCCS1 ILWJAOPQHOZXAN-UHFFFAOYSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 229940095564 anhydrous calcium sulfate Drugs 0.000 description 2
- 238000010560 atom transfer radical polymerization reaction Methods 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 229920001688 coating polymer Polymers 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 230000001404 mediated effect Effects 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 description 2
- 125000005496 phosphonium group Chemical group 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000011164 primary particle Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000004445 quantitative analysis Methods 0.000 description 2
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000002076 thermal analysis method Methods 0.000 description 2
- 125000000101 thioether group Chemical group 0.000 description 2
- 125000003396 thiol group Chemical group [H]S* 0.000 description 2
- FLOJNXXFMHCMMR-UHFFFAOYSA-N 1,3-dithiolanyl Chemical group [CH]1SCCS1 FLOJNXXFMHCMMR-UHFFFAOYSA-N 0.000 description 1
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
- KLIDCXVFHGNTTM-UHFFFAOYSA-N 2,6-dimethoxyphenol Chemical compound COC1=CC=CC(OC)=C1O KLIDCXVFHGNTTM-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- SCVJRXQHFJXZFZ-KVQBGUIXSA-N 2-amino-9-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purine-6-thione Chemical compound C1=2NC(N)=NC(=S)C=2N=CN1[C@H]1C[C@H](O)[C@@H](CO)O1 SCVJRXQHFJXZFZ-KVQBGUIXSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- QWOVZHUJHAFOJS-UHFFFAOYSA-N 4-amino-2-(4-sulfophenyl)benzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C(C=2C=CC(=CC=2)S(O)(=O)=O)=C1 QWOVZHUJHAFOJS-UHFFFAOYSA-N 0.000 description 1
- UNYIAFAXSZQQOZ-UHFFFAOYSA-N 4-aminobutane-1,3-disulfonic acid Chemical compound NCC(S(O)(=O)=O)CCS(O)(=O)=O UNYIAFAXSZQQOZ-UHFFFAOYSA-N 0.000 description 1
- XRUKRHLZDVJJSX-UHFFFAOYSA-N 4-cyanopentanoic acid Chemical compound N#CC(C)CCC(O)=O XRUKRHLZDVJJSX-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 238000004438 BET method Methods 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 239000004908 Emulsion polymer Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 101001024616 Homo sapiens Neuroblastoma breakpoint family member 9 Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004609 Impact Modifier Substances 0.000 description 1
- 240000004343 Indigofera suffruticosa Species 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical group SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- PPUXIFZWLZSTJT-UHFFFAOYSA-N NC(C=C1C2=CC(S(O)(=O)=O)=CC=C2)=CC(S(O)(=O)=O)=C1O Chemical compound NC(C=C1C2=CC(S(O)(=O)=O)=CC=C2)=CC(S(O)(=O)=O)=C1O PPUXIFZWLZSTJT-UHFFFAOYSA-N 0.000 description 1
- 229910052779 Neodymium Inorganic materials 0.000 description 1
- 102100037013 Neuroblastoma breakpoint family member 9 Human genes 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical class OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 229920001153 Polydicyclopentadiene Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 241000872198 Serjania polyphylla Species 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 101000983338 Solanum commersonii Osmotin-like protein OSML15 Proteins 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 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
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000012935 ammoniumperoxodisulfate Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 235000015241 bacon Nutrition 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000005874 benzothiadiazolyl group Chemical group 0.000 description 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 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
- 238000004040 coloring Methods 0.000 description 1
- 229920000891 common polymer Polymers 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000006258 conductive agent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 208000012839 conversion disease Diseases 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 150000003983 crown ethers Chemical class 0.000 description 1
- YQHLDYVWEZKEOX-UHFFFAOYSA-N cumene hydroperoxide Chemical compound OOC(C)(C)C1=CC=CC=C1 YQHLDYVWEZKEOX-UHFFFAOYSA-N 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- LFINSDKRYHNMRB-UHFFFAOYSA-N diazanium;oxido sulfate Chemical compound [NH4+].[NH4+].[O-]OS([O-])(=O)=O LFINSDKRYHNMRB-UHFFFAOYSA-N 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000001599 direct drying Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-M ethenesulfonate Chemical compound [O-]S(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-M 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229910001448 ferrous ion Inorganic materials 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 238000004442 gravimetric analysis Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000005549 heteroarylene group Chemical group 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000010952 in-situ formation Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 159000000014 iron salts Chemical class 0.000 description 1
- QHDRKFYEGYYIIK-UHFFFAOYSA-N isovaleronitrile Chemical compound CC(C)CC#N QHDRKFYEGYYIIK-UHFFFAOYSA-N 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 238000011177 media preparation Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229960005141 piperazine Drugs 0.000 description 1
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004597 plastic additive Substances 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920002189 poly(glycerol 1-O-monomethacrylate) polymer Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000867 polyelectrolyte Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- LLBIOIRWAYBCKK-UHFFFAOYSA-N pyranthrene-8,16-dione Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3C=C4C5=CC=CC=C5C(=O)C5=C4C4=C3C2=C1C=C4C=C5 LLBIOIRWAYBCKK-UHFFFAOYSA-N 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 125000001422 pyrrolinyl group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000007717 redox polymerization reaction Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000010512 small scale reaction Methods 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 150000003613 toluenes Chemical class 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/08—Ingredients agglomerated by treatment with a binding agent
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/44—Carbon
- C09C1/48—Carbon black
- C09C1/56—Treatment of carbon black ; Purification
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2002/00—Crystal-structural characteristics
- C01P2002/80—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70
- C01P2002/88—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70 by thermal analysis data, e.g. TGA, DTA, DSC
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/01—Particle morphology depicted by an image
- C01P2004/04—Particle morphology depicted by an image obtained by TEM, STEM, STM or AFM
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
- Y10T428/2998—Coated including synthetic resin or polymer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/30—Self-sustaining carbon mass or layer with impregnant or other layer
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Polymerisation Methods In General (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10411798P | 1998-10-13 | 1998-10-13 | |
| US60/104,117 | 1998-10-13 | ||
| US09/317,706 US6458458B1 (en) | 1998-10-13 | 1999-05-24 | Polymer coated carbon products and other pigments and methods of making same by aqueous media polymerizations or solvent coating methods |
| US09/317,706 | 1999-05-24 | ||
| PCT/US1999/023429 WO2000022051A1 (en) | 1998-10-13 | 1999-10-08 | Polymer coated carbon products and other pigments and methods of making same by aqueous media polymerizations or solvent coating methods |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011278264A Division JP2012072414A (ja) | 1998-10-13 | 2011-12-20 | ポリマー被覆の炭素生成物及びその他の顔料並びに水性媒質重合法又は溶媒コーティング法によるそれらの製造法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002527564A true JP2002527564A (ja) | 2002-08-27 |
| JP2002527564A5 JP2002527564A5 (enExample) | 2006-11-30 |
Family
ID=26801197
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000575948A Withdrawn JP2002527564A (ja) | 1998-10-13 | 1999-10-08 | ポリマー被覆の炭素生成物及びその他の顔料並びに水性媒質重合法又は溶媒コーティング法によるそれらの製造法 |
| JP2011278264A Pending JP2012072414A (ja) | 1998-10-13 | 2011-12-20 | ポリマー被覆の炭素生成物及びその他の顔料並びに水性媒質重合法又は溶媒コーティング法によるそれらの製造法 |
| JP2014266662A Pending JP2015110785A (ja) | 1998-10-13 | 2014-12-26 | ポリマー被覆の炭素生成物及びその他の顔料並びに水性媒質重合法又は溶媒コーティング法によるそれらの製造法 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011278264A Pending JP2012072414A (ja) | 1998-10-13 | 2011-12-20 | ポリマー被覆の炭素生成物及びその他の顔料並びに水性媒質重合法又は溶媒コーティング法によるそれらの製造法 |
| JP2014266662A Pending JP2015110785A (ja) | 1998-10-13 | 2014-12-26 | ポリマー被覆の炭素生成物及びその他の顔料並びに水性媒質重合法又は溶媒コーティング法によるそれらの製造法 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6458458B1 (enExample) |
| EP (1) | EP1124905B1 (enExample) |
| JP (3) | JP2002527564A (enExample) |
| KR (1) | KR100639724B1 (enExample) |
| AT (1) | ATE331000T1 (enExample) |
| AU (1) | AU6421299A (enExample) |
| CA (1) | CA2347093C (enExample) |
| DE (1) | DE69932071T2 (enExample) |
| ES (1) | ES2262344T3 (enExample) |
| WO (1) | WO2000022051A1 (enExample) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005007760A1 (ja) * | 2003-07-23 | 2005-01-27 | Toagosei Co., Ltd. | 水性インク |
| JP2008501814A (ja) * | 2004-06-02 | 2008-01-24 | ユニヴェルシテ パリ セット−デニス ディデロ | 表面改質材料、その製造方法及びその使用 |
| JP2008530306A (ja) * | 2005-02-11 | 2008-08-07 | カーネギー メロン ユニバーシティ | 改質された炭素粒子 |
| JP2008242495A (ja) * | 2001-05-15 | 2008-10-09 | E Ink Corp | 電気泳動粒子 |
| JP2009518459A (ja) * | 2005-10-26 | 2009-05-07 | アルシメール | 絶縁体表面又は半導体表面を修飾する方法、及びこうして得られた生成物 |
| JP2010513647A (ja) * | 2006-12-19 | 2010-04-30 | コミッサリア タ レネルジー アトミーク | 非電気化学的条件下での固体支持体表面への有機フィルムの調製方法、このように得られた固体支持体、および調製キット |
| JP2010254568A (ja) * | 2009-04-24 | 2010-11-11 | Qinghua Univ | Ｃｎｔカプセル及びその製造方法、複合材料体 |
| JP2013119577A (ja) * | 2011-12-06 | 2013-06-17 | Toyota Central R&D Labs Inc | 樹脂複合材料およびその製造方法 |
Families Citing this family (77)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7002728B2 (en) | 1997-08-28 | 2006-02-21 | E Ink Corporation | Electrophoretic particles, and processes for the production thereof |
| US7247379B2 (en) | 1997-08-28 | 2007-07-24 | E Ink Corporation | Electrophoretic particles, and processes for the production thereof |
| EP1157069B1 (en) | 1999-03-05 | 2003-05-07 | Cabot Corporation | Process for preparing colored pigments |
| DE60036866T2 (de) | 1999-03-12 | 2008-07-31 | Cabot Corp., Boston | Kationische pigmente und diese enthaltende wässrige zusammensetzungen |
| JP4851040B2 (ja) | 1999-10-28 | 2012-01-11 | キャボット コーポレイション | インクジェット用インク、インク、および着色顔料を含有するその他の組成物 |
| AU1353501A (en) | 1999-10-28 | 2001-05-08 | Cabot Corporation | Ink jet inks, inks, and other compositions containing colored pigments |
| EP1244906A1 (en) | 1999-12-30 | 2002-10-02 | Cabot Corporation | Sensors with improved properties |
| CN1234780C (zh) | 2000-01-07 | 2006-01-04 | 卡伯特公司 | 连接在颜料上的聚合物和其它基团以及后续反应 |
| WO2001055245A2 (en) | 2000-01-25 | 2001-08-02 | Cabot Corporation | Polymers containing modified pigments and methods of preparing the same |
| WO2001097965A1 (fr) * | 2000-06-19 | 2001-12-27 | Bridgestone Corporation | Adsorbant, son procede d'obtention et ses applications |
| KR100831782B1 (ko) * | 2000-07-06 | 2008-05-27 | 캐보트 코포레이션 | 개질된 안료 생성물을 포함하는 인쇄판 |
| US6929889B2 (en) * | 2000-07-06 | 2005-08-16 | Cabot Corporation | Modified pigment products, dispersions thereof, and compositions comprising the same |
| US6822781B1 (en) | 2000-10-24 | 2004-11-23 | Cabot Corporation | Gyricon displays containing modified particles |
| EP1355998B1 (en) * | 2001-02-02 | 2006-04-05 | Cabot Corporation | Ink compositions comprising salts with polyvalent ions |
| US7230750B2 (en) | 2001-05-15 | 2007-06-12 | E Ink Corporation | Electrophoretic media and processes for the production thereof |
| DE10120821A1 (de) * | 2001-04-27 | 2002-10-31 | Sachtleben Chemie Gmbh | Mit Polyalken beschichtete, poröse Füllstoffe |
| US6712894B2 (en) | 2001-05-09 | 2004-03-30 | Cabot Corporation | Method of producing secure images using inks comprising modified pigment particles |
| US6641653B2 (en) | 2001-07-19 | 2003-11-04 | Cabot Corporation | Ink compositions comprising modified colored pigments and methods for preparing the same |
| KR100437224B1 (ko) * | 2001-08-29 | 2004-06-23 | 주식회사 태평양 | 자외선 산란용 무기/고분자 복합입자 및 그의 제조방법 |
| US20030050361A1 (en) * | 2001-09-05 | 2003-03-13 | Eastman Kodak Company | Ink jet ink composition |
| US6641656B2 (en) | 2001-10-17 | 2003-11-04 | Cabot Corporation | Dispersions comprising modified pigments |
| JP2006503114A (ja) * | 2002-01-07 | 2006-01-26 | キャボット コーポレイション | 改質ピグメント生成物およびそれを含むブラックマトリクス |
| US7001934B2 (en) * | 2002-01-24 | 2006-02-21 | Cabot Coroporation | Inkjet ink systems comprising a gelling agent |
| CN1297597C (zh) * | 2002-03-27 | 2007-01-31 | 卡伯特公司 | 连接一种或多种有机基团到颗粒上的方法 |
| US7173078B2 (en) | 2002-04-12 | 2007-02-06 | Cabot Corporation | Process for preparing modified pigments |
| US6699319B2 (en) | 2002-05-06 | 2004-03-02 | Cabot Corporation | Process for preparing modified pigments |
| US6833026B2 (en) | 2002-05-10 | 2004-12-21 | Cabot Corporation | Modified pigments and process for preparing modified pigments |
| CA2411443A1 (en) * | 2002-11-07 | 2004-05-07 | Formmat Technologies Inc. | Method to produce graphite/polymer composites |
| US6936097B2 (en) * | 2003-04-16 | 2005-08-30 | Cabot Corporation | Modified organic colorants and dispersions, and methods for their preparation |
| US6942724B2 (en) * | 2003-04-16 | 2005-09-13 | Cabot Corporation | Modified organic colorants and dispersions, and methods for their preparation |
| US20050221139A1 (en) * | 2004-03-15 | 2005-10-06 | Hampden-Smith Mark J | Modified carbon products, their use in bipolar plates and similar devices and methods relating to same |
| US20050256225A1 (en) * | 2004-05-11 | 2005-11-17 | Viola Michael S | Aqueous inkjet ink compositions comprising comb-branched copolymers |
| CN101371194B (zh) * | 2004-10-15 | 2012-01-04 | 卡伯特公司 | 高电阻率组合物 |
| JP5086096B2 (ja) * | 2004-12-17 | 2012-11-28 | キャボット コーポレイション | 多層顔料を含むインクジェットインキ |
| US20060144410A1 (en) * | 2004-12-30 | 2006-07-06 | Philip Morris Usa Inc. | Surface-modified activated carbon in smoking articles |
| JP5280846B2 (ja) * | 2005-07-22 | 2013-09-04 | キャボット コーポレイション | 顔料組成物の製造法 |
| KR101338798B1 (ko) | 2005-10-31 | 2013-12-06 | 캐보트 코포레이션 | 변성 착색제, 및 변성 착색제를 포함하는 잉크젯 잉크조성물 |
| CN102304300B (zh) * | 2006-04-03 | 2016-04-27 | 悉尼大学 | 聚合物包封的固体颗粒材料及包含其的离散颗粒 |
| WO2008055244A2 (en) | 2006-10-31 | 2008-05-08 | Sensient Colors Inc. | Modified pigments and methods for making and using the same |
| FR2910006B1 (fr) * | 2006-12-19 | 2009-03-06 | Commissariat Energie Atomique | Procede de preparation d'un film organique a la surface d'un support solide dans des conditions non-electrochimiques, support solide ainsi obtenu et kit de preparation |
| US9725602B2 (en) * | 2006-12-19 | 2017-08-08 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Method for preparing an organic film at the surface of a solid support under non-electrochemical conditions, solid support thus obtained and preparation kit |
| FR2910007B1 (fr) * | 2006-12-19 | 2009-03-06 | Commissariat Energie Atomique | Procede de preparation d'un film organique a la surface d'un support solide dans des conditions non-electrochimiques, support solide ainsi obtenu et kit de preparation |
| WO2008091653A2 (en) * | 2007-01-24 | 2008-07-31 | Cabot Corporation | Process to form modified pigments |
| CN101675130A (zh) * | 2007-02-27 | 2010-03-17 | 卡伯特公司 | 包含多种改性颜料的喷墨油墨组合物 |
| US8133311B2 (en) * | 2007-04-30 | 2012-03-13 | Cabot Corporation | Pigment dipsersions comprising functionalized non-polymeric dispersants |
| CN101855302B (zh) | 2007-08-23 | 2014-10-01 | 森馨颜色公司 | 自分散颜料及制造和使用该自分散颜料的方法 |
| US20090192248A1 (en) * | 2007-12-07 | 2009-07-30 | Palumbo Paul S | Method of preparing a pigment composition |
| US20090155508A1 (en) | 2007-12-14 | 2009-06-18 | Pactiv Corporation | Encapsulated Activated Carbon and the Preparation Thereof |
| WO2009117071A1 (en) * | 2008-03-17 | 2009-09-24 | Cabot Corporation | Modified pigments having reduced phosphate release, and dispersions and inkjet ink compositions therefrom |
| US8129448B2 (en) * | 2008-12-18 | 2012-03-06 | Cabot Corporation | Method of preparing polymer modified pigments |
| JP2012514683A (ja) * | 2009-01-09 | 2012-06-28 | キャボット コーポレイション | 低減された導電率増加を有する改質顔料含有インクジェットインク組成物 |
| US20100227162A1 (en) * | 2009-03-03 | 2010-09-09 | Abhimanyu Onkar Patil | Atom transfer radical polymerization (ATRP) based inorganic polymer structures |
| KR20110135989A (ko) | 2009-04-07 | 2011-12-20 | 센션트 컬러스 엘엘씨 | 자가-분산 입자 및 그의 제조 및 사용 방법 |
| US9644042B2 (en) | 2010-12-17 | 2017-05-09 | Carnegie Mellon University | Electrochemically mediated atom transfer radical polymerization |
| US8435707B2 (en) | 2011-06-16 | 2013-05-07 | Cabot Corporation | Toner additive comprising carbon-silica dual phase particles |
| EP2734583B1 (en) | 2011-07-22 | 2020-03-18 | Cabot Corporation | High resistivity coating compositions having unique percolation behavior, and electrostatic image developing systems and components thereof incorporating same |
| US20140275420A1 (en) | 2011-08-22 | 2014-09-18 | Carnegie Mellon University | Atom transfer radical polymerization under biologically compatible conditions |
| WO2013126745A2 (en) | 2012-02-23 | 2013-08-29 | Carnegie Mellon University | Ligands designed to provide highly active catalyst complexes |
| KR101391825B1 (ko) * | 2012-05-21 | 2014-05-12 | (주)고딘테크 | 그라핀-공중합체 나노복합체 제조 방법 |
| WO2014012597A1 (en) * | 2012-07-20 | 2014-01-23 | Hewlett-Packard Indigo B.V. | Polymerically coated metallic pigment particles, method for providing them and electrostatic inks |
| US20140120339A1 (en) | 2012-10-31 | 2014-05-01 | Cabot Corporation | Porous carbon monoliths templated by pickering emulsions |
| EP2945994B1 (en) | 2013-01-18 | 2018-07-11 | Basf Se | Acrylic dispersion-based coating compositions |
| EP3038836B1 (en) | 2013-08-28 | 2021-10-06 | Hewlett-Packard Development Company, L.P. | Printable recording media |
| TWI519608B (zh) * | 2013-12-27 | 2016-02-01 | 財團法人工業技術研究院 | 混成碳黑、及包含其之塗佈組合物與遮光材料 |
| EP4194087A1 (en) | 2014-04-29 | 2023-06-14 | Archer-Daniels-Midland Company | Catalyst comprising a shaped porous carbon product |
| US11253839B2 (en) | 2014-04-29 | 2022-02-22 | Archer-Daniels-Midland Company | Shaped porous carbon products |
| MX2017000470A (es) * | 2014-07-15 | 2017-03-08 | Imerys Graphite & Carbon Switzerland Ltd | Material carbonoso de superficie hidrofilica modificada. |
| US9982070B2 (en) | 2015-01-12 | 2018-05-29 | Carnegie Mellon University | Aqueous ATRP in the presence of an activator regenerator |
| TWI565655B (zh) * | 2015-09-25 | 2017-01-11 | 財團法人工業技術研究院 | 混成碳黑與塗佈組合物 |
| US10722867B2 (en) | 2015-10-28 | 2020-07-28 | Archer-Daniels-Midland Company | Porous shaped carbon products |
| US10464048B2 (en) | 2015-10-28 | 2019-11-05 | Archer-Daniels-Midland Company | Porous shaped metal-carbon products |
| WO2018132582A1 (en) | 2017-01-12 | 2018-07-19 | Carnegie Mellon University | Surfactant assisted formation of a catalyst complex for emulsion atom transfer radical polymerization processes |
| US11185845B1 (en) | 2017-12-07 | 2021-11-30 | U.S. Government As Represented By The Secretary Of The Army | Water extractable microcapsules of activated carbon, super activated carbon, and other adsorptive and reactive materials |
| JP6796107B2 (ja) * | 2018-05-16 | 2020-12-02 | 旭化成株式会社 | セルロース含有樹脂組成物の製造方法 |
| JP6964646B2 (ja) * | 2018-05-16 | 2021-11-10 | 旭化成株式会社 | セルロース含有樹脂組成物の製造方法 |
| CN108864774B (zh) * | 2018-07-20 | 2020-01-07 | 江南大学 | 一种棉织物染色用反应性自分散纳米炭黑的制备方法 |
| WO2021236586A1 (en) | 2020-05-18 | 2021-11-25 | Archer-Daniels-Midland Company | Processes for the hydrogenolysis of glycerol |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04234467A (ja) * | 1990-08-31 | 1992-08-24 | Xerox Corp | 修飾顔料粒子を含有するインク組成物 |
| JPH093354A (ja) * | 1995-06-14 | 1997-01-07 | Nippon Shokubai Co Ltd | 着色剤組成物 |
| JPH09124969A (ja) * | 1995-10-30 | 1997-05-13 | Mitsubishi Chem Corp | 絶縁性ブラックマトリックス用カーボンブラック |
| JPH09324134A (ja) * | 1996-02-15 | 1997-12-16 | Ricoh Co Ltd | 処理カーボンブラック顔料および該顔料を含有する静電荷像現像用トナー |
| WO1997047691A1 (en) * | 1996-06-14 | 1997-12-18 | Cabot Corporation | Modified carbon products and amphiphilic ions containing compositions |
| JPH1090691A (ja) * | 1996-09-11 | 1998-04-10 | Natoko Paint Kk | 液晶用着色遮光スペーサーおよび液晶表示素子 |
| JPH1095943A (ja) * | 1996-09-24 | 1998-04-14 | Citizen Watch Co Ltd | 水性顔料系記録液 |
| JP2000095987A (ja) * | 1998-07-31 | 2000-04-04 | Hewlett Packard Co <Hp> | 共有結合で付着されたポリマ―をもつ変性巨大分子発色団を含むインクジェット用インク組成物 |
Family Cites Families (62)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2439442A (en) | 1943-02-06 | 1948-04-13 | Cabot Godfrey L Inc | Process of making hydrophilic carbon black |
| US2502254A (en) | 1945-12-07 | 1950-03-28 | Ici Ltd | Manufacture of pigments |
| US2514236A (en) | 1948-03-12 | 1950-07-04 | Ici Ltd | Manufacture of pigments |
| US2867540A (en) | 1955-12-30 | 1959-01-06 | Monsanto Chemicals | Modified carbon black product and process |
| DE1082045B (de) | 1958-01-30 | 1960-05-19 | Hoechst Ag | Faerbung von plastischen Massen |
| GB910309A (en) | 1958-07-22 | 1962-11-14 | Dunlop Rubber Co | Rubber compositions |
| US3043708A (en) | 1958-07-22 | 1962-07-10 | Dunlop Rubber Co | Modified carbon black |
| US3335020A (en) | 1964-03-02 | 1967-08-08 | Huber Corp J M | Modified carbon blacks |
| US3479300A (en) | 1965-10-22 | 1969-11-18 | Cabot Corp | Carbonaceous products |
| US3471439A (en) | 1966-03-10 | 1969-10-07 | Amicon Corp | Reinforcing filler |
| US4014844A (en) | 1970-06-26 | 1977-03-29 | Agence Nationale De Valorisation De La Recherche (Anvar) | Process for grafting polymers on carbon black through free radical mechanism |
| US3755244A (en) | 1971-06-02 | 1973-08-28 | Hercules Inc | Polyolefin pigment dispersions |
| US3884871A (en) | 1973-06-29 | 1975-05-20 | Nl Industries Inc | Process for coating pigment particles with organic polymers |
| GB1589960A (en) | 1977-06-02 | 1981-05-20 | Bayer Ag | Dyestuff formulations |
| GB2036779B (en) | 1978-11-22 | 1983-03-09 | Bayer Ag | Polyether disazo dyestuffs |
| DE2850662A1 (de) | 1978-11-22 | 1980-06-12 | Bayer Ag | Polyaetherfarbstoffe, praeparationen dieser farbstoffe, deren herstellung sowie deren verwendung |
| DE3049180A1 (de) | 1980-12-24 | 1982-07-29 | Cassella Ag, 6000 Frankfurt | Wasserunloesliche monoazofarbstoffe, ihre herstellung und ihre verwendung |
| US4758243A (en) | 1986-05-27 | 1988-07-19 | Milliken Research Corporation | Process for coloring polyester shaped articles |
| US4880857A (en) | 1986-12-17 | 1989-11-14 | Nippon Shokubai Kagaku Kogyo Co., Ltd. | Carbon black-graft polymer, method for production thereof, and use thereof |
| US4871371A (en) | 1988-10-24 | 1989-10-03 | Milliken Research Corporation | Tint compositions useful for providing coloration to aqueous and non-aqueous liquids |
| US4946509A (en) | 1989-05-23 | 1990-08-07 | Sun Chemical Corporation | Diarylide pigment compositions |
| ATE145232T1 (de) | 1990-01-08 | 1996-11-15 | Milliken Res Corp | Zwischenprodukte und farbstoffe mit vermehrt primären hydroxylgruppen enthaltenden poly(oxyalkylen)-resten sowie deren herstellung |
| JPH0428776A (ja) | 1990-05-24 | 1992-01-31 | Mitsubishi Kasei Corp | インクジェット用記録液 |
| JP3004062B2 (ja) | 1991-02-06 | 2000-01-31 | 株式会社日本触媒 | インキ及びインキ用着色剤 |
| CA2050019A1 (en) | 1991-08-27 | 1993-02-28 | John Bery Hines | Colorants and intermediates therefor having branched poly(oxyalkylene) moieties, and their manufacture |
| ZA933185B (en) * | 1992-05-08 | 1994-05-23 | Dick Co Ab | Encapsulated magnetic particles pigments and carbon black compositions and methods related thereto |
| US5298356A (en) | 1992-11-13 | 1994-03-29 | Eastman Kodak Company | Toner composition with elastomeric thermoplastic polymer and process of preparing |
| IL116376A (en) | 1994-12-15 | 2001-03-19 | Cabot Corp | Aqueous ink jet ink compositions containing modified carbon products |
| US5559169A (en) | 1994-12-15 | 1996-09-24 | Cabot Corporation | EPDM, HNBR and Butyl rubber compositions containing carbon black products |
| US5554739A (en) | 1994-12-15 | 1996-09-10 | Cabot Corporation | Process for preparing carbon materials with diazonium salts and resultant carbon products |
| IL116377A (en) | 1994-12-15 | 2003-05-29 | Cabot Corp | Reaction of carbon black with diazonium salts, resultant carbon black products and their uses |
| US5571311A (en) | 1994-12-15 | 1996-11-05 | Cabot Corporation | Ink jet ink formulations containing carbon black products |
| IL116379A (en) | 1994-12-15 | 2003-12-10 | Cabot Corp | Aqueous inks and coatings containing modified carbon products |
| US5807494A (en) | 1994-12-15 | 1998-09-15 | Boes; Ralph Ulrich | Gel compositions comprising silica and functionalized carbon products |
| IL116552A (en) | 1995-01-10 | 2001-09-13 | Cabot Corp | Carbon black compositions, polymer compositions including the carbon black compositions and articles of manufacture including the polymer compositions |
| US5869550A (en) | 1995-05-22 | 1999-02-09 | Cabot Corporation | Method to improve traction using silicon-treated carbon blacks |
| EP0787777A4 (en) * | 1995-06-14 | 2001-10-04 | Nippon Catalytic Chem Ind | GASKET POLYMER CONTAINING SOOT |
| US6017584A (en) | 1995-07-20 | 2000-01-25 | E Ink Corporation | Multi-color electrophoretic displays and materials for making the same |
| US5747559A (en) | 1995-11-22 | 1998-05-05 | Cabot Corporation | Polymeric compositions |
| JPH09292703A (ja) | 1996-04-25 | 1997-11-11 | Mitsubishi Chem Corp | レーザーダイレクト湿し水不要感光性平版印刷版 |
| US5747562A (en) * | 1996-06-14 | 1998-05-05 | Cabot Corporation | Ink and coating compositions containing silicon-treated carbon black |
| US5707432A (en) | 1996-06-14 | 1998-01-13 | Cabot Corporation | Modified carbon products and inks and coatings containing modified carbon products |
| KR100463354B1 (ko) * | 1996-06-14 | 2005-06-16 | 캐보트 코포레이션 | 개질탄소생성물및양친매성이온함유조성물 |
| US6069190A (en) * | 1996-06-14 | 2000-05-30 | Cabot Corporation | Ink compositions having improved latency |
| US6110994A (en) * | 1996-06-14 | 2000-08-29 | Cabot Corporation | Polymeric products containing modified carbon products and methods of making and using the same |
| US5837045A (en) | 1996-06-17 | 1998-11-17 | Cabot Corporation | Colored pigment and aqueous compositions containing same |
| US6103782A (en) * | 1996-07-29 | 2000-08-15 | Marconi Data Systems, Inc. | Method of making dry pigment surface modified with polyethylene coating |
| JPH1053722A (ja) * | 1996-08-12 | 1998-02-24 | Yokohama Rubber Co Ltd:The | ゴム補強用表面処理カーボンブラックの製造方法 |
| AU4737997A (en) | 1996-09-25 | 1998-04-17 | Cabot Corporation | Silica coated carbon blacks |
| US5930026A (en) | 1996-10-25 | 1999-07-27 | Massachusetts Institute Of Technology | Nonemissive displays and piezoelectric power supplies therefor |
| US5919855A (en) | 1997-02-11 | 1999-07-06 | Cabot Corporation | Use of modified carbon black in gas-phase polymerizations |
| US5783614A (en) | 1997-02-21 | 1998-07-21 | Copytele, Inc. | Polymeric-coated dielectric particles and formulation and method for preparing same |
| US5961804A (en) | 1997-03-18 | 1999-10-05 | Massachusetts Institute Of Technology | Microencapsulated electrophoretic display |
| US6017980A (en) * | 1997-03-27 | 2000-01-25 | Cabot Corporation | Elastomeric compounds incorporating metal-treated carbon blacks |
| US6020063A (en) * | 1997-07-31 | 2000-02-01 | Virginia Tech Intellectual Properties, Inc. | Composites of thermosetting resins and carbon fibers having polyhydroxyether sizings |
| US5932633A (en) | 1997-08-22 | 1999-08-03 | Copytele, Inc. | Method for making polymers-coated pigment particles using initiator-treated pigments |
| US5964935A (en) | 1997-08-22 | 1999-10-12 | Copytele, Inc. | Initiator-treated pigment particles and method for preparing same |
| US5990202A (en) | 1997-10-31 | 1999-11-23 | Hewlett-Packard Company | Dual encapsulation technique for preparing ink-jets inks |
| US6057384A (en) | 1997-10-31 | 2000-05-02 | Hewlett-Packard Company | Latex polymer blends for improving the permanence of ink-jet inks |
| US6103380A (en) * | 1998-06-03 | 2000-08-15 | Cabot Corporation | Particle having an attached halide group and methods of making the same |
| EP0976798B1 (en) * | 1998-07-31 | 2004-07-07 | Hewlett-Packard Company, A Delaware Corporation | Covalent attachment of polymers onto macromolecular chromophores by nucleophilic substitution reaction for inkjet printing |
| US6479571B1 (en) | 2000-01-25 | 2002-11-12 | Cabot Corporation | Elastomeric compositions containing polymer coated carbon products and other pigments |
-
1999
- 1999-05-24 US US09/317,706 patent/US6458458B1/en not_active Expired - Lifetime
- 1999-10-08 WO PCT/US1999/023429 patent/WO2000022051A1/en not_active Ceased
- 1999-10-08 JP JP2000575948A patent/JP2002527564A/ja not_active Withdrawn
- 1999-10-08 CA CA002347093A patent/CA2347093C/en not_active Expired - Fee Related
- 1999-10-08 KR KR1020017004653A patent/KR100639724B1/ko not_active Expired - Fee Related
- 1999-10-08 DE DE69932071T patent/DE69932071T2/de not_active Expired - Lifetime
- 1999-10-08 AU AU64212/99A patent/AU6421299A/en not_active Abandoned
- 1999-10-08 EP EP99951860A patent/EP1124905B1/en not_active Expired - Lifetime
- 1999-10-08 AT AT99951860T patent/ATE331000T1/de not_active IP Right Cessation
- 1999-10-08 ES ES99951860T patent/ES2262344T3/es not_active Expired - Lifetime
-
2011
- 2011-12-20 JP JP2011278264A patent/JP2012072414A/ja active Pending
-
2014
- 2014-12-26 JP JP2014266662A patent/JP2015110785A/ja active Pending
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04234467A (ja) * | 1990-08-31 | 1992-08-24 | Xerox Corp | 修飾顔料粒子を含有するインク組成物 |
| JPH093354A (ja) * | 1995-06-14 | 1997-01-07 | Nippon Shokubai Co Ltd | 着色剤組成物 |
| JPH09124969A (ja) * | 1995-10-30 | 1997-05-13 | Mitsubishi Chem Corp | 絶縁性ブラックマトリックス用カーボンブラック |
| JPH09324134A (ja) * | 1996-02-15 | 1997-12-16 | Ricoh Co Ltd | 処理カーボンブラック顔料および該顔料を含有する静電荷像現像用トナー |
| WO1997047691A1 (en) * | 1996-06-14 | 1997-12-18 | Cabot Corporation | Modified carbon products and amphiphilic ions containing compositions |
| JP2000512327A (ja) * | 1996-06-14 | 2000-09-19 | キャボット コーポレイション | 修飾炭素生成物及び両親媒性イオン含有組成物 |
| JPH1090691A (ja) * | 1996-09-11 | 1998-04-10 | Natoko Paint Kk | 液晶用着色遮光スペーサーおよび液晶表示素子 |
| JPH1095943A (ja) * | 1996-09-24 | 1998-04-14 | Citizen Watch Co Ltd | 水性顔料系記録液 |
| JP2000095987A (ja) * | 1998-07-31 | 2000-04-04 | Hewlett Packard Co <Hp> | 共有結合で付着されたポリマ―をもつ変性巨大分子発色団を含むインクジェット用インク組成物 |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008242495A (ja) * | 2001-05-15 | 2008-10-09 | E Ink Corp | 電気泳動粒子 |
| WO2005007760A1 (ja) * | 2003-07-23 | 2005-01-27 | Toagosei Co., Ltd. | 水性インク |
| JP2008501814A (ja) * | 2004-06-02 | 2008-01-24 | ユニヴェルシテ パリ セット−デニス ディデロ | 表面改質材料、その製造方法及びその使用 |
| JP2012102330A (ja) * | 2004-06-02 | 2012-05-31 | Univ Paris 7-Denis Diderot | 表面改質材料、その製造方法及びその使用 |
| JP2008530306A (ja) * | 2005-02-11 | 2008-08-07 | カーネギー メロン ユニバーシティ | 改質された炭素粒子 |
| JP2009518459A (ja) * | 2005-10-26 | 2009-05-07 | アルシメール | 絶縁体表面又は半導体表面を修飾する方法、及びこうして得られた生成物 |
| JP2010513647A (ja) * | 2006-12-19 | 2010-04-30 | コミッサリア タ レネルジー アトミーク | 非電気化学的条件下での固体支持体表面への有機フィルムの調製方法、このように得られた固体支持体、および調製キット |
| JP2010254568A (ja) * | 2009-04-24 | 2010-11-11 | Qinghua Univ | Ｃｎｔカプセル及びその製造方法、複合材料体 |
| JP2013119577A (ja) * | 2011-12-06 | 2013-06-17 | Toyota Central R&D Labs Inc | 樹脂複合材料およびその製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE69932071D1 (de) | 2006-08-03 |
| ATE331000T1 (de) | 2006-07-15 |
| JP2012072414A (ja) | 2012-04-12 |
| WO2000022051A1 (en) | 2000-04-20 |
| JP2015110785A (ja) | 2015-06-18 |
| CA2347093C (en) | 2009-04-07 |
| KR100639724B1 (ko) | 2006-10-30 |
| CA2347093A1 (en) | 2000-04-20 |
| US6458458B1 (en) | 2002-10-01 |
| KR20010085918A (ko) | 2001-09-07 |
| EP1124905B1 (en) | 2006-06-21 |
| AU6421299A (en) | 2000-05-01 |
| DE69932071T2 (de) | 2006-11-23 |
| ES2262344T3 (es) | 2006-11-16 |
| EP1124905A1 (en) | 2001-08-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2002527564A (ja) | ポリマー被覆の炭素生成物及びその他の顔料並びに水性媒質重合法又は溶媒コーティング法によるそれらの製造法 | |
| US6479571B1 (en) | Elastomeric compositions containing polymer coated carbon products and other pigments | |
| EP1040160B1 (en) | Polymeric products containing modified carbon products and methods of making and using the same | |
| US6472471B2 (en) | Polymeric products containing modified carbon products and methods of making and using the same | |
| JP2001521972A (ja) | 結合した安定型フリーラジカルを持つ粒子、重合変性粒子、及びその製造方法 | |
| CN110791121B (zh) | 具有耐光高分散稳定性的杂化有机颜料粉体的制备方法 | |
| CN102510868B (zh) | 在含水碱性条件下可溶的(甲基)丙烯酸酯共聚物的本体聚合 | |
| JP6513335B2 (ja) | 分散剤及び固体粒子分散体 | |
| JPS6128434A (ja) | 分散安定剤とその使用 | |
| CN113549312B (zh) | 一种抗菌阻燃抗静电pc/abs组合物及其制备方法和应用 | |
| KR20200103669A (ko) | 폴리카보네이트 배합물을 개질하는 방법 | |
| JPH044323B2 (enExample) | ||
| CA1309795C (en) | Water soluble polymers | |
| JPH01138271A (ja) | 表面処理された有機顔料の製造方法 | |
| JPS63286470A (ja) | 表面処理されたカ−ボンブラックの製造方法 | |
| BR112020010966A2 (pt) | método para produzir uma composição polimérica, e, dispersão de partículas de poliolefina reticuladas em um meio aquoso | |
| HK1033330B (en) | Polymeric products containing modified carbon products and methods of making and using the same | |
| JPH02105869A (ja) | カーボンブラック | |
| PH26053A (en) | Water soluble polymers and dispersion containing them | |
| MXPA99007403A (en) | Water-based emulsion polymers which resist blocking |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20061004 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20061004 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20100629 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20100929 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20101006 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20101227 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20110823 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20111220 |
|
| A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20120104 |
|
| A761 | Written withdrawal of application |
Free format text: JAPANESE INTERMEDIATE CODE: A761 Effective date: 20120130 |