JP2006106198A5 - - Google Patents

Info

Publication number

JP2006106198A5

JP2006106198A5 JP2004290438A JP2004290438A JP2006106198A5 JP 2006106198 A5 JP2006106198 A5 JP 2006106198A5 JP 2004290438 A JP2004290438 A JP 2004290438A JP 2004290438 A JP2004290438 A JP 2004290438A JP 2006106198 A5 JP2006106198 A5 JP 2006106198A5

Authority

JP

Japan

Prior art keywords

pigment

pigment yellow

toner according

pigment red

yellow

Prior art date

2004-10-01

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Pending

Links

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• 239000000049 pigment Substances 0.000 claims 49
• 238000004519 manufacturing process Methods 0.000 claims 8
• 150000001451 organic peroxides Chemical class 0.000 claims 7
• 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 claims 5
• 239000000843 powder Substances 0.000 claims 5
• 239000000178 monomer Substances 0.000 claims 4
• 239000002245 particle Substances 0.000 claims 4
• 229920002554 vinyl polymer Polymers 0.000 claims 4
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
• 238000006116 polymerization reaction Methods 0.000 claims 3
• 239000003086 colorant Substances 0.000 claims 2
• VPWFPZBFBFHIIL-UHFFFAOYSA-L disodium 4-[(4-methyl-2-sulfophenyl)diazenyl]-3-oxidonaphthalene-2-carboxylate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC(C)=CC=C1N=NC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 VPWFPZBFBFHIIL-UHFFFAOYSA-L 0.000 claims 2
• 239000000155 melt Substances 0.000 claims 2
• 239000000203 mixture Substances 0.000 claims 2
• 230000000379 polymerizing effect Effects 0.000 claims 2
• 239000011347 resin Substances 0.000 claims 2
• 229920005989 resin Polymers 0.000 claims 2
• 229920002545 silicone oil Polymers 0.000 claims 2
• 229910052717 sulfur Inorganic materials 0.000 claims 2
• 125000004434 sulfur atom Chemical group 0.000 claims 2
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 2
• SOFRHZUTPGJWAM-UHFFFAOYSA-N 3-hydroxy-4-[(2-methoxy-5-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound COc1ccc(cc1N=Nc1c(O)c(cc2ccccc12)C(=O)Nc1cccc(c1)[N+]([O-])=O)[N+]([O-])=O SOFRHZUTPGJWAM-UHFFFAOYSA-N 0.000 claims 1
• COHYTHOBJLSHDF-UHFFFAOYSA-N Indigo Chemical compound N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 claims 1
• 239000012736 aqueous medium Substances 0.000 claims 1
• PZTQVMXMKVTIRC-UHFFFAOYSA-L chembl2028348 Chemical compound [Ca+2].[O-]S(=O)(=O)C1=CC(C)=CC=C1N=NC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 PZTQVMXMKVTIRC-UHFFFAOYSA-L 0.000 claims 1
• 239000003795 chemical substances by application Substances 0.000 claims 1
• 230000009477 glass transition Effects 0.000 claims 1
• 235000019239 indanthrene blue RS Nutrition 0.000 claims 1
• 229940104573 pigment red 5 Drugs 0.000 claims 1
• 239000003505 polymerization initiator Substances 0.000 claims 1
• 239000011164 primary particle Substances 0.000 claims 1
• WPPDXAHGCGPUPK-UHFFFAOYSA-N red 2 Chemical compound C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=2C=3C4=CC=C5C6=CC=C7C8=C(C=9C=CC=CC=9)C9=CC=CC=C9C(C=9C=CC=CC=9)=C8C8=CC=C(C6=C87)C(C=35)=CC=2)C4=C1C1=CC=CC=C1 WPPDXAHGCGPUPK-UHFFFAOYSA-N 0.000 claims 1
• 229910000077 silane Inorganic materials 0.000 claims 1
• -1 silane compound Chemical class 0.000 claims 1
• 238000010558 suspension polymerization method Methods 0.000 claims 1