WO2000005313A1 - Hydrophobic modification of chargeable pigment particles - Google Patents
Hydrophobic modification of chargeable pigment particles Download PDFInfo
- Publication number
- WO2000005313A1 WO2000005313A1 PCT/GB1999/002378 GB9902378W WO0005313A1 WO 2000005313 A1 WO2000005313 A1 WO 2000005313A1 GB 9902378 W GB9902378 W GB 9902378W WO 0005313 A1 WO0005313 A1 WO 0005313A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- pigment
- pigment particles
- polar
- suspension
- maleic anhydride
- Prior art date
Links
- 239000000049 pigment Substances 0.000 title claims abstract description 135
- 239000002245 particle Substances 0.000 title claims abstract description 65
- 230000002209 hydrophobic effect Effects 0.000 title claims abstract description 19
- 230000004048 modification Effects 0.000 title description 11
- 238000012986 modification Methods 0.000 title description 11
- 239000000725 suspension Substances 0.000 claims abstract description 64
- 238000000034 method Methods 0.000 claims abstract description 38
- 229920000642 polymer Polymers 0.000 claims abstract description 33
- 239000012454 non-polar solvent Substances 0.000 claims abstract description 21
- 239000002952 polymeric resin Substances 0.000 claims abstract description 18
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 18
- 238000004873 anchoring Methods 0.000 claims abstract description 13
- 239000006229 carbon black Substances 0.000 claims description 25
- -1 aldehydo Chemical group 0.000 claims description 16
- 125000000524 functional group Chemical group 0.000 claims description 14
- 238000003801 milling Methods 0.000 claims description 12
- 239000000178 monomer Substances 0.000 claims description 12
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 9
- 229920001400 block copolymer Polymers 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 5
- 229920000578 graft copolymer Polymers 0.000 claims description 5
- 150000001336 alkenes Chemical class 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 3
- 229930194542 Keto Natural products 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 125000000468 ketone group Chemical group 0.000 claims description 3
- 150000003573 thiols Chemical class 0.000 claims description 3
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 2
- 125000003368 amide group Chemical group 0.000 claims 2
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 125000001261 isocyanato group Chemical group *N=C=O 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- 239000002904 solvent Substances 0.000 description 16
- 238000004062 sedimentation Methods 0.000 description 13
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 12
- 102000029749 Microtubule Human genes 0.000 description 9
- 108091022875 Microtubule Proteins 0.000 description 9
- 210000004688 microtubule Anatomy 0.000 description 9
- 239000011521 glass Substances 0.000 description 6
- 239000011324 bead Substances 0.000 description 5
- 238000005191 phase separation Methods 0.000 description 5
- 239000013049 sediment Substances 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 230000005684 electric field Effects 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000006664 bond formation reaction Methods 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000000412 dendrimer Substances 0.000 description 3
- 229920000736 dendritic polymer Polymers 0.000 description 3
- 238000003795 desorption Methods 0.000 description 3
- 238000005189 flocculation Methods 0.000 description 3
- 230000016615 flocculation Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000976 ink Substances 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229920000141 poly(maleic anhydride) Polymers 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- SVGUNYFQHHUNDJ-UHFFFAOYSA-N (6-fluoro-1-benzothiophen-2-yl)boronic acid Chemical compound C1=C(F)C=C2SC(B(O)O)=CC2=C1 SVGUNYFQHHUNDJ-UHFFFAOYSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-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
- CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 1
- KLBVIRPOVIVOLL-UHFFFAOYSA-N 3-hydroxy-4-[[4-[4-[[2-hydroxy-3-[(2-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]-N-(2-methoxyphenyl)naphthalene-2-carboxamide Chemical compound COc1ccccc1NC(=O)c1cc2ccccc2c(N=Nc2ccc(cc2OC)-c2ccc(N=Nc3c(O)c(cc4ccccc34)C(=O)Nc3ccccc3OC)c(OC)c2)c1O KLBVIRPOVIVOLL-UHFFFAOYSA-N 0.000 description 1
- QDPSGELUBXFKSB-UHFFFAOYSA-N 4-[(4-aminophenyl)diazenyl]naphthalen-1-amine Chemical compound C1=CC(N)=CC=C1N=NC1=CC=C(N)C2=CC=CC=C12 QDPSGELUBXFKSB-UHFFFAOYSA-N 0.000 description 1
- IYHIFXGFKVJNBB-UHFFFAOYSA-N 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonic acid Chemical compound C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S(O)(=O)=O IYHIFXGFKVJNBB-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- BVTJGGGYKAMDBN-UHFFFAOYSA-N Dioxetane Chemical group C1COO1 BVTJGGGYKAMDBN-UHFFFAOYSA-N 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical group 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- HBHZKFOUIUMKHV-UHFFFAOYSA-N chembl1982121 Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O HBHZKFOUIUMKHV-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001687 destabilization Effects 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000009881 electrostatic interaction Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000006355 external stress Effects 0.000 description 1
- 150000002194 fatty esters Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000008040 ionic compounds Chemical class 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- PYUYQYBDJFMFTH-WMMMYUQOSA-N naphthol red Chemical compound CCOC1=CC=CC=C1NC(=O)C(C1=O)=CC2=CC=CC=C2\C1=N\NC1=CC=C(C(N)=O)C=C1 PYUYQYBDJFMFTH-WMMMYUQOSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000001208 nuclear magnetic resonance pulse sequence Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Chemical group 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920001291 polyvinyl halide Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- 230000001360 synchronised effect Effects 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- 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
- 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
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/10—Treatment with macromolecular organic compounds
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/10—Solid density
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/12—Surface area
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/90—Other properties not specified above
Definitions
- the present invention relates to hydrophobic modification of chargeable pigment particles and non-polar suspensions of such pigment particles.
- Stable suspensions of chargeable pigment particles are desirable in certain applications wherein the formation of images (permanent or latent) requires charging or discharging the pigment particles.
- Such applications include liquid toners, ink jet inks using solvents and electrostatic paints.
- the preparation of such suspensions has been documented in literature.
- To stabilize hydrophilic pigments in non-polar solvents, steric barriers are introduced to provide stabilization. Common strategies to do so include the use of ionic surfactants or polymeric dispersants which adsorb on the pigment (e.g., U.S. Patents 5,536,615 and 5,482,809); dendrimers (e.g., U.S.
- Patent 5,558,968 or non-polymeric resins (e.g., U.S. Patent 5,521,046) to modify the pigment surface.
- polymeric dyes U.S. Patents 5,521,271 and 5,563,024
- their inferior lightfastness and weatherability coupled with their relatively high production costs, have restricted their usage.
- Stable suspensions of chargeable pigment particles in non-polar solvents is difficult to prepare, mainly for two reasons.
- chargeable pigment particles contain surface polar functional groups like carboxylic acid.
- these polar functional groups also make the pigment hydrophilic.
- the hydrophilicity of the pigment particles causes them to be attracted to each other rather than to the non-polar solvent, resulting in flocculation and destabilization of the pigment suspension.
- surfactants are used to provide steric stabilization in suspending such particles.
- the polar ends of the surfactants adsorb onto the hydrophilic pigment surface, and the hydrophobic portion is solvated by the non-polar solvent. This mode of weak attachment leads to flocculation and degradation of the non-polar suspension.
- a disadvantage of using physically adsorbed surfactants or dispersants in suspensions is that under external stress, like a high electric field, some of these suspensions or formulations become unstable. This is due to the dissociation or desorption of a surfactant or resin from the pigment particle surface.
- dendrimers that are covalently bonded to pigment surfaces partially addresses the problem of desorption, but the process of assembling such a complex molecular architecture on the pigment surface translates into a lengthy preparation and high production cost.
- a method for making a non-polar suspension of chargeable pigment particles comprising ( 1 ) forming a suspension of pigment particles in a non-polar solvent, wherein the pigment particles are inherently ionic or are chargeable and possess surface anchoring groups on the surface of the pigment particles; and (2) contacting the pigment particles with a polymeric resin comprising a hydrophobic region and a reactive group that reacts with the surface-anchoring groups on the surface of the pigment particle.
- the surface anchoring group and the polymeric resin can form a covalent or hydrogen bonding, preferably a covalent bond.
- the polymeric resin preferably comprises a maleic anhydride group.
- the present invention further provides a non-polar suspension of inherently ionic or chargeable pigment particles having surface-anchoring groups on the surface of the particles.
- the suspension comprises the pigment particles suspended in a non-polar solvent, wherein the pigment particles have on their surface a polymeric resin that comprises a hydrophobic region and a reactive group that reacts with the surface-anchoring groups on the pigment surface.
- the present invention further provides a method of hydrophobically modifying chargeable pigment particles having a first functional group, the method comprising contacting the pigment particles with a polymer having a hydrophobic region and a second functional group in such a way as to form a covalent bond between the first and second functional groups.
- the pigment particles for modification according to the present invention advantageously have two desirable properties: chargeability and susceptibility to being modified.
- Chargeability is imparted by the reactive or functional groups present on the pigment.
- chargeable pigments can be divided into two categories.
- the first category includes pigments that are inherently ionic in character. Examples of this type of pigment include complexes of transitional metals, e.g., iron blue; and ionic compounds, e.g., calcium sulfate. Some pigments contain residual ionic species on their surface, as a result of an inefficient washing process.
- pigments may be used in the present process, since the ionic species on the pigment surface are not bound tightly on the surface, they may be lost or washed off during the process steps, and hence chargeability of such pigments may not be satisfactory and may vary from batch to batch.
- the second category of chargeable pigments includes pigments that are not inherently ionic and yet possess chargeable groups on the surface. These groups include, but are not limited to, carboxylic groups, hydroxyl groups including phenolic hydroxyl groups, alkyl hydroxyl groups, and alkenyl hydroxyl groups, amino groups which may be primary, secondary, tertiary or quaternary ammonium groups, quinoline groups, and other functional groups that contain heteroatoms such as nitrogen, oxygen, or sulfur. Examples of pigments possessing such groups include oxidized carbon black. A particularly suitable oxidized carbon black pigment is FXTM 200 supplied by Degussa Company (Ridgefield Park, NJ).
- oxidized carbon black contains carboxyl, hydroxyl, keto, aldehyde, and/or other chargeable groups.
- pigments include Hansa Yellow, Dinitroaniline Orange, Naphthol Red, Red Lake C, Lith ⁇ l Red, Rubine Red, Dianisidine Blue, Alizarin Lake, and Nickel Azo Yello, which bear hydroxyl groups, and Disperse Yellow 9, Disperse Black 1, and Solvent Brown, which bear amino groups.
- the second property desirable in a pigment is its susceptibility or reactivity to permit surface modification.
- the pigments should possess surface reactive groups such as, carboxylic groups, hydroxyl groups, amino groups, quinoline groups, thiol groups, epoxy groups, or dioxetane groups.
- the polymeric resin used to modify the surface of the pigment preferably should meet two criteria. First, it should have a functional group that can react with the surface anchoring groups of the pigment. Such functional groups include hydroxy, carboxylic acid, carboxy anhydride, thiols, amino, amide, mono or di- substituted amide, isocyanide, isocyanate, and the like.
- Copolymers composed of a reactive polar monomer and a hydrophobic monomer are particularly useful as modifying polymeric resins.
- reactive polar monomers include maleic anhydride, acrylic acid, acrylamide, aldehyde containing monomers, amine or amide containing monomers, hydroxyalkyl acrylates, and epoxy containing monomers.
- Maleic anhydride is a preferred monomer.
- hydrophobic monomers include alkenes such as ethylene, propylene, and butylene, substituted alkenes such as styrene, acrylic esters, vinyl ethers, vinyl alkanes, and vinyl halides. Styrene is a preferred hydrophobic monomer.
- the copolymers can be blocked, graft, random, statistical, or alternate. Block and graft copolymers are further preferred. Block copolymers can be di, tri, tetra, or multiblock.
- An example of a suitable block copolymer is polymaleic anhydride-b/ ⁇ c£-polyethylene (Aldrich Chemical Co., Milwaukee, WI), which is useful, for example, for modifying and suspending carbon black in paraffinic solvents.
- the maleic anhydride functionality can react with the surface groups of the carbon black, particularly the hydroxyl groups to form a covalent bond.
- the polyethylene portion provides suspendability in paraffinic solvents.
- polystyrene-b/ ⁇ cfc-maleic anhydride examples include polystyrene-b/ ⁇ cfc-maleic anhydride; graft polymers such as polyethylene-gr ⁇ /t-polymaleic anhydride; polycycloalkylethylene-gr ⁇ t-polymaleic anhydride, like polycyclohexylethylene-gra/t-maleic anhydride; and polymaleic anhydride-gr t-polyacrylate, like polymaleic anhydride-gr ⁇ t-polymethylacrylate.
- graft polymers such as polyethylene-gr ⁇ /t-polymaleic anhydride; polycycloalkylethylene-gr ⁇ t-polymaleic anhydride, like polycyclohexylethylene-gra/t-maleic anhydride; and polymaleic anhydride-gr t-polyacrylate, like polymaleic anhydride-gr ⁇ t-polymethylacrylate.
- a covalent bond is formed between the reactive groups of the polymer resin and those of the pigment particles.
- the covalent bond formation can be confirmed by methods known to those of ordinary skill in the art, for example, by infrared spectroscopy.
- the formation of a covalent bond formation can be confirmed by the appearance of infrared absorption peaks corresponding to the ester carbonyl and carboxyl carbonyl and the disappearance of the carbonyl peaks due to the anhydride groups.
- the polymer when it is covalently bound to a pigment would not be removed from the pigment by repeated washing with a solvent for the free or unbound polymer. This lack of solubility of the bound polymer can be used as a means for confirming or identifying covalent bond formation.
- the polymer preferably has a molecular weight from about 15,000 to about 200,000, more desirably from about 15,000 to about 100,000. Even higher molecular weight polymers may be employed; however, the amount of polymer needs to be controlled to avoid processing difficulties due to the high viscosities generally expected of high molecular weight polymers.
- the quantity of polymer used would also depend upon factors such as the specific gravity and the surface area of the pigment. Usually the amount of polymer will be from about 1 to about 99 percent, and preferably ranges between about 30 and about 50 percent based on the weight of the pigment.
- the suiface modification would to alter the density of the pigment.
- the density of the modified pigment can be less than that of the pigment itself. This reduction in density is an advantage; it helps in stabilizing suspensions in non-polar solvents by bringing down the density of the pigment close to that of the solvent. Since the density of the surface modifying polymer is generally less than that of heavy or high density pigments, such as titanium dioxide, heavy pigments tend to require more polymer, whereas light pigments, e.g., carbon black, may require a quantity of polymer closer to the low end of this range.
- solvents examples include non-polar, aprotic solvents, such as saturated aliphatic solvents, like Isopar G (Exxon Chemical Co., Houston, TX); saturated cyclic aliphatic solvents like decahydronaphthalene and cyclohexane (both from Aldrich Chemical Co.); mixtures of both aliphatic and cyclic aliphatic solvents like VMP Naphtha (Ashland Chemical Co., Chicago, IL); aromatic solvents like toluene or xylene (both from Aldrich Chemical Co.); and halogenated hydrocarbons like chloroform and dichloroethane (both from Aldrich Chemical Co.).
- non-polar, aprotic solvents such as saturated aliphatic solvents, like Isopar G (Exxon Chemical Co., Houston, TX); saturated cyclic aliphatic solvents like decahydronaphthalene and cyclohexane (both from Aldrich Chemical Co.); mixture
- the preparation of the non-polar suspensions of the present invention involves the following steps: milling and surface modification. Milling may be performed by any known technique, including using a glass jar charged with glass beads, or a media mill.
- the usual milling medium of choice is glass beads. For most applications, glass beads of 2 mm diameter are sufficient. If a smaller particle size is desired, zirconium beads with a diameter less than 1 mm can be used.
- the particle size of the suspended particles can be monitored periodically to determine the desired milling time. Milling can be stopped when no more changes in the particle size occurs. Depending upon the hardness of the pigment, typical milling times range from about one hour to about two hours.
- the final particle size of the pigment particles is controlled by the size of the milling media and the time of milling.
- the modified pigment particles may be recovered, as by filtration, and washed to separate the pigments particles from the suspension medium. Such modified pigment particles may be used as such or resuspended in another suitable non-polar vehicle.
- the stability and chargeability of the pigment suspensions can be determined by any method known to those of ordinary skill in the art.
- a simple way to study suspension stability is by placing the suspension in a graduate cylinder and observing if a phase separation occurs. If the suspension is not stable, phase separation will occur, forming a supernatant layer which is depleted in pigment and leaving a pigment sediment at the bottom of the container. The volumes or the heights of the supernatant and the sediment can be measured.
- one can compare the relative stability of pigment suspensions by (1) observing whether phase separation occurs or not; and (2) comparing the time for the phase separation to happen.
- Another method of measuring suspension stability involves the use of an instrument which provides a quantitative measure of the sedimentation rate, e.g., a BYK Chemie Dynometer Type 191 0 (Silver Spring, MD).
- This method involves measuring the weight of the sediment phase separating out over a given period of time on a sedimentation disk positioned within the suspension with its concave suiface facing upwards.
- a stable suspension would have a sedimentation rate of less than about 15 mg per hour, preferably close to zero mg per hour.
- the chargeability or the ability of the pigment suspension to respond to an external electric field can be determined as follows.
- the direction of migration of particles depends upon their net suiface charge and the polarities of the electrodes.
- the synchronized movement of the particles will generate an impression that the whole microtubule is vibrating periodically between the two electrodes.
- the minimum potential difference, or minimum voltage, across the electrodes needed to cause the particles to migrate would be inversely proportional to the charges induced on or carried by the individual pigment particle.
- Pigment particles that are highly charged or are easily chargeable would require a lower minimum voltage to migrate. Consequently, when compared among a series of samples, the minimum or threshold voltage to cause such changes will give the relative chargeability or suiface charges of the pigment particles.
- the minimum voltage can be measured by methods known to those of ordinary skill in the art.
- a solution of a non-polar suspension is placed in a microtubule, such as the one available from Viprocom Co. in Mountain Lake, NJ.
- the microtubule is then placed between two parallel copper electrodes mounted on an acrylic plate.
- the whole set-up is then placed under a microscope.
- a pulsating voltage with a square wave form is applied across the electrode and changes in the appearance of the tube are noted.
- the minimum voltage that causes migration of the particles is also noted.
- a similar method is described in Y. Hirobe et al., IS&T's Eighth Int'l Congress on Advances in Non-Impact Printing Technologies, page 198 (1992).
- EXAMPLE 1 This Example illustrates a method of modifying oxidized carbon black using a poly(styrene- c ⁇ -maleic anhydride) and a method of preparing a non-polar suspension of the modified oxidized carbon black.
- This Example illustrates a method of modifying oxidized carbon black using a polyethylene- gra/t-maleic anhydride polymer and a method of preparing a non-polar suspension of the modified pigment.
- Example 1 The procedure in Example 1 was followed except that a polyethylene-gr ⁇ /t-maleic anhydride (Aldrich Catalog No. 44240-2) was used as the modifying polymer. Decahydronaphthalene (Koch Chemical, Corpus Christi, TX) was used as the non-polar solvent. A modified pigment and a non- polar suspension were obtained.
- a polyethylene-gr ⁇ /t-maleic anhydride Aldrich Catalog No. 44240-2
- Decahydronaphthalene Koch Chemical, Corpus Christi, TX
- a modified pigment and a non- polar suspension were obtained.
- EXAMPLE 3 This Example illustrates an advantage of using a high molecular weight polymeric resin to modify oxidized carbon black. Thus, for comparative purposes, modification was carried out using a poly(styrene-c ⁇ -maleic anhydride) of a molecular weight lower than that of the polymer employed in Example 1.
- Example 1 The procedure of Example 1 was followed but poly(styrene ⁇ c ⁇ -maleic anhydride) of molecular weight 1 ,900 (Aldrich Catalog No.42650-4) was employed instead of the polymer of MW 200,000, and a modified pigment was obtained.
- the sedimentation rate of a non-polar suspension was measured as follows. The amount of the sediment formed was recorded as a function of time using a BYK Chemie Dynometer Type 191 0 (Silver Spring, MD). The rate was determined by dividing the amount of sediment collected by the elapsed time. The accuracy of measurement is +/- 1.0 mg per hour.
- the sedimentation rates of non-polar suspensions prepared as illustrated in Examples 1 and 3 were measured and the results obtained are set forth in Table 1. Table 1. Sedimentation rates of non-polar suspensions of Examples 1 and 3.
- EXAMPLE 4 This Example illustrates the suitability of the modified pigments of the present invention for preparing stable non-polar suspensions in several non-polar solvents.
- Non-polar suspensions were prepared using the modified pigment of Example 1 in cyclohexane, toluene, and VMP naphtha.
- the suspensions contained 3% by weight of carbon black,
- Two copper strips each with dimensions of 1 cm x 5 cm x 0.012 cm, were mounted end to end onto an acrylic plate.
- the gap between the ends of the strips was about 120 microns.
- the copper strip ends away from the gap were connected to a power supply with a Model 7500 amplifier (Krohn-hite, Avon, MA) and a function generator (Model 95, Wavetek, San Diego, CA).
- a pigment suspension prepared from the modified carbon black in Example 2 in decahydronaphthalene was placed in a Viprocom microtubule which was later placed in the gap between the copper strips. The whole assembly was then placed on the sample stage of a microscope. The function generator delivered a pulsating electric field across the gap. As the pulse sequence was initiated, any change in appearance of the contents of the microtubule was noted. The voltage was increased slowly until a "vibrating motion" was observed in the microtubule. The minimum voltage needed to effect such a change was recorded. It was observed that the pigment was chargeable as shown the vibrating motion of the contents of the microtubule at the minimum voltage. The experiment was repeated with non-polar suspensions containing the pigment of Example 2 in toluene or VMP naphtha, and the minimum voltage to cause a vibrating motion of the microtubule was noted. The results obtained are set forth in Table 3.
- the foregoing shows that the modified pigment of the present invention is chargeable.
- the foregoing further shows that the chargeability of the pigments can be influenced by the suspension medium.
- the modified pigments were more chargeable in a higher dielectric medium (toluene or decahydronaphthalene) than in a lower dielectric medium (VMP naphtha).
- This Example illustrates another advantage of the surface modification of the present invention.
- a polymer that forms a covalent bond with a pigment is superior in modifying the pigment and in providing a stable non-polar suspension compared to a polymer that physically adsorbs and does not form a covalent bond with the pigment.
- a suspension of oxidized carbon black was prepared as in Example 1 except that the poly(styrene-c ⁇ -maleic anhydride) was replaced by a commonly used modifier, SOLOSPERSETM 17940 (Zeneca, Wilmington, DE).
- This modifier is believed to be a block copolymer of polymeric fatty ester containing proprietary anchoring groups with one end of the polymer capable of being adsorbed physically onto the pigment and the other end capable of being solvated by the non-polar solvent.
- the stability of this suspension was compared with that of the non-polar suspension of Example 1. The sedimentation rates were measured and the results obtained are set forth in Table 4.
- a pigment modified with a polymer that formed a covalent bond with the pigment forms a more stable suspension compared to a pigment modified by a polymer that physically adsorbs on the polymer.
- This Example illustrates the stability of the modification when a covalent bond is formed between the pigment and the modifying polymer.
- a polyethylene-gra/t-maleic anhydride was used to modify oxidized carbon black as illustrated in Example 2.
- the modified pigment was separated from the solvent by filtration and the filtered pigment was washed with decahydronaphthalene 16 times.
- the washed pigment formed a stable suspension in a non-polar solvent, thereby confirming that the polymer was not removed by the washing.
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU50551/99A AU5055199A (en) | 1998-07-24 | 1999-07-22 | Hydrophobic modification of chargeable pigment particles |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/122,164 | 1998-07-24 | ||
US09/122,164 US6235829B1 (en) | 1998-07-24 | 1998-07-24 | Modification of chargeable pigment particles |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000005313A1 true WO2000005313A1 (en) | 2000-02-03 |
Family
ID=22401091
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB1999/002378 WO2000005313A1 (en) | 1998-07-24 | 1999-07-22 | Hydrophobic modification of chargeable pigment particles |
Country Status (3)
Country | Link |
---|---|
US (1) | US6235829B1 (en) |
AU (1) | AU5055199A (en) |
WO (1) | WO2000005313A1 (en) |
Cited By (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001051566A1 (en) * | 2000-01-07 | 2001-07-19 | Cabot Corporation | Polymers and other groups attached to pigments and subsequent reactions |
WO2001074119A1 (en) * | 2000-03-24 | 2001-10-04 | World Properties, Inc. | Polymeric organic coatings and method of manufacture thereof |
WO2002004210A1 (en) * | 2000-07-06 | 2002-01-17 | Cabot Corporation | Printing plates comprising modified pigment products |
EP1134261A3 (en) * | 2000-03-16 | 2003-10-29 | Degussa AG | Carbon black |
US6641656B2 (en) | 2001-10-17 | 2003-11-04 | Cabot Corporation | Dispersions comprising modified pigments |
US6641653B2 (en) | 2001-07-19 | 2003-11-04 | Cabot Corporation | Ink compositions comprising modified colored pigments and methods for preparing the same |
US6699319B2 (en) | 2002-05-06 | 2004-03-02 | Cabot Corporation | Process for preparing modified pigments |
US6712894B2 (en) | 2001-05-09 | 2004-03-30 | Cabot Corporation | Method of producing secure images using inks comprising modified pigment particles |
US6833026B2 (en) | 2002-05-10 | 2004-12-21 | Cabot Corporation | Modified pigments and process for preparing modified pigments |
US6929889B2 (en) | 2000-07-06 | 2005-08-16 | Cabot Corporation | Modified pigment products, dispersions thereof, and compositions comprising the same |
US7001934B2 (en) | 2002-01-24 | 2006-02-21 | Cabot Coroporation | Inkjet ink systems comprising a gelling agent |
US7537650B2 (en) | 2005-03-30 | 2009-05-26 | Eastman Kodak Company | Aqueous ink of colored ink and colorless ink containing anionic polymer |
WO2010138191A1 (en) | 2009-05-29 | 2010-12-02 | Eastman Kodak Company | Aqueous compositions with improved silicon corrosion characteristics |
WO2011066117A1 (en) | 2009-11-24 | 2011-06-03 | Eastman Kodak Company | Continuous inkjet printer aquous ink composition |
WO2011066091A1 (en) | 2009-11-24 | 2011-06-03 | Eastman Kodak Company | Continuous inkjet printer aqueous ink composition |
WO2011146323A1 (en) | 2010-05-17 | 2011-11-24 | Eastman Kodak Company | Inkjet recording medium and methods therefor |
WO2012030546A1 (en) | 2010-08-31 | 2012-03-08 | Eastman Kodak Company | Inkjet printing fluid |
WO2012030553A2 (en) | 2010-08-31 | 2012-03-08 | Eastman Kodak Company | Recirculating fluid printing system and method |
WO2012087542A2 (en) | 2010-12-20 | 2012-06-28 | Eastman Kodak Company | Inkjet ink composition with jetting aid |
WO2012134783A2 (en) | 2011-03-31 | 2012-10-04 | Eastman Kodak Company | Inkjet printing ink set |
WO2012149324A1 (en) | 2011-04-29 | 2012-11-01 | Eastman Kodak Company | Recirculating inkjet printing fluid, system and method |
WO2013032826A1 (en) | 2011-08-31 | 2013-03-07 | Eastman Kodak Company | Continuous inkjet printing method and fluid set |
WO2013112440A1 (en) | 2012-01-24 | 2013-08-01 | Eastman Kodak Company | Ink having antibacterial and antifungal protection |
WO2013112400A2 (en) | 2012-01-24 | 2013-08-01 | Eastman Kodak Company | Antibacterial and antifungal protection for ink jet image |
WO2013165882A1 (en) | 2012-05-02 | 2013-11-07 | Eastman Kodak Company | Inkjet receiving medium and pre-treatment composition for inkjet printing |
WO2015199983A1 (en) | 2014-06-23 | 2015-12-30 | Eastman Kodak Company | Recirculating inkjet printing fluid |
Families Citing this family (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020147252A1 (en) * | 2001-02-02 | 2002-10-10 | Adams Curtis E. | Ink compositions comprising salts with polyvalent ions |
WO2002093246A1 (en) * | 2001-05-15 | 2002-11-21 | E Ink Corporation | Electrophoretic particles |
WO2003057784A2 (en) * | 2002-01-07 | 2003-07-17 | Cabot Corporation | Modified pigment products and black matrixes comprising same |
US7173078B2 (en) | 2002-04-12 | 2007-02-06 | Cabot Corporation | Process for preparing modified pigments |
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 |
US7001936B2 (en) * | 2003-07-16 | 2006-02-21 | Lexmark International, Inc. | Pigmented inkjet ink |
US7148268B2 (en) * | 2003-10-24 | 2006-12-12 | Videojet Technologies Inc. | Opaque ink jet ink composition |
US7897658B2 (en) * | 2003-10-28 | 2011-03-01 | Cabot Corporation | Aqueous coating compositions |
US7495042B2 (en) * | 2003-10-28 | 2009-02-24 | Cabot Corporation | Non-aqueous coating compositions |
EP1702014A1 (en) * | 2004-01-06 | 2006-09-20 | Videojet Technologies Inc. | Indelible ink jet ink composition |
US20050256225A1 (en) * | 2004-05-11 | 2005-11-17 | Viola Michael S | Aqueous inkjet ink compositions comprising comb-branched copolymers |
EP1810079B1 (en) * | 2004-10-15 | 2014-08-20 | Cabot Corporation | High resistivity compositions |
EP1833931B1 (en) * | 2004-12-17 | 2012-08-01 | Cabot Corporation | Inkjet inks comprising multi-layer pigments |
US20060162612A1 (en) * | 2005-01-25 | 2006-07-27 | Kabalnov Alexey S | Pigments modified with surface counter-ions |
WO2007014007A2 (en) * | 2005-07-22 | 2007-02-01 | Cabot Corporation | Method of preparing pigment compositions |
US8585816B2 (en) * | 2006-05-16 | 2013-11-19 | Cabot Corporation | Low viscosity, high particulate loading dispersions |
US8728223B2 (en) | 2006-05-16 | 2014-05-20 | Cabot Corporation | Low viscosity, high particulate loading dispersions |
US7785410B2 (en) * | 2006-06-30 | 2010-08-31 | Videojet Technologies Inc. | Ink jet ink composition and method for printing on substrates under conditions of high static electrical charge |
US7947124B2 (en) * | 2006-06-30 | 2011-05-24 | Videojet Technologies Inc. | High electrical resistivity ink jet ink composition |
US7740694B2 (en) * | 2006-06-30 | 2010-06-22 | Videojet Technologies Inc | Ink jet ink composition and method for printing |
US7520926B2 (en) * | 2006-09-15 | 2009-04-21 | Videojet Technologies Inc. | Solvent-based ink composition |
JP2010516860A (en) * | 2007-01-24 | 2010-05-20 | キャボット コーポレイション | Method for producing modified pigments |
JP2011506635A (en) * | 2007-12-07 | 2011-03-03 | キャボット コーポレイション | Method for preparing pigment composition |
US8129448B2 (en) * | 2008-12-18 | 2012-03-06 | Cabot Corporation | Method of preparing polymer modified pigments |
EP2443521A4 (en) * | 2009-06-19 | 2012-11-28 | Cabot Corp | Chemical toners comprising modified pigments |
CN114736533B (en) * | 2022-04-13 | 2023-11-17 | 苏州世名科技股份有限公司 | Surface modified organic pigment, modification method, application and color master batch containing surface modified organic pigment |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1514922A (en) * | 1974-06-19 | 1978-06-21 | Ici Ltd | Siliceous materials |
WO1987005924A1 (en) * | 1986-04-04 | 1987-10-08 | Revertex Limited | Dispersions of solids in organic liquids |
EP0787777A1 (en) * | 1995-06-14 | 1997-08-06 | Nippon Shokubai Co., Ltd. | Carbon black graft polymer, process for the production of the polymer and use thereof |
Family Cites Families (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1046723A (en) | 1963-01-02 | 1966-10-26 | Lajos Csonka | Process for preparing surface treated pigments |
GB1104939A (en) | 1964-06-10 | 1968-03-06 | Laporte Titanium Ltd | Improvements in and relating to the treatment of pigments |
US3398113A (en) | 1964-12-01 | 1968-08-20 | Chemetron Corp | Thermosetting resin pigment composition and process therefor |
CH533670A (en) | 1968-12-05 | 1973-02-15 | Ciba Geigy Ag | Inorganic white pigments containing optical brighteners |
DE2043629A1 (en) | 1970-09-03 | 1972-03-16 | Degussa | Hydrophobicising finely divided oxides - with silazanes in a fluidise bed reactor |
DE2313073C2 (en) | 1973-03-16 | 1984-11-29 | Istvan Prof. Dr. 6600 Saarbruecken Halasz | Process for the chemical modification of surfaces of inorganic solids and their use |
GB1494746A (en) | 1974-08-06 | 1977-12-14 | Ferro Ltd | Coated pigments |
JPS5182317A (en) | 1975-01-17 | 1976-07-19 | Masayoshi Sakakibara | IBUNSANSEIRYUJOKONJOSOSEIBUTSUOYOBISONOSEIHO |
US4160760A (en) | 1977-08-22 | 1979-07-10 | Northwestern University | Process for preparing polyacrylonitrile doped with Prussion blue |
US4277288A (en) | 1978-10-06 | 1981-07-07 | Ciba-Geigy Corporation | Fluidized granulation of pigments using organic granulating assistant |
US4327011A (en) | 1979-11-20 | 1982-04-27 | Century Inks Corporation | Printing ink and vehicle therefor |
JPS59170130A (en) | 1983-03-17 | 1984-09-26 | Daihachi Kagaku Kogyosho:Kk | Plastic or rubber magnet composition |
JPS59170131A (en) | 1983-03-17 | 1984-09-26 | Daihachi Kagaku Kogyosho:Kk | Surface-modified inorganic powder |
DE3334596A1 (en) | 1983-09-24 | 1985-04-18 | Merck Patent Gmbh, 6100 Darmstadt | DISPERSABLE BERLIN BLUE PIGMENT |
JPS6079068A (en) | 1983-10-05 | 1985-05-04 | Kawaken Fine Chem Co Ltd | Method for modifying surface of powdered material having hydrophilic surface |
JPS62267368A (en) | 1986-05-15 | 1987-11-20 | Nippon Oil & Fats Co Ltd | Surface-treating agent for iron oxide-based pigment |
US4755563A (en) | 1986-12-29 | 1988-07-05 | E. I. Du Pont De Nemours And Company | Block copolymer dispersants containing ionic moieties |
DE3726048A1 (en) | 1987-08-06 | 1989-02-16 | Bayer Ag | THERMOSTABLE IRON OXID PIGMENTS, METHOD FOR THE PRODUCTION AND USE THEREOF |
JP2691438B2 (en) | 1989-01-16 | 1997-12-17 | 大日精化工業株式会社 | Method for producing colored spherical polymer particles |
DE4002008A1 (en) | 1990-01-24 | 1991-07-25 | Henkel Kgaa | OLEFINICALLY UNSATURATED ADDUCTS OF PROPYLENE TO MULTIPLE UNSATURATED FATTY ACIDS OR. FATTY ACID ESTERS, METHOD FOR THEIR PRODUCTION AND THEIR USE |
CA2048183A1 (en) | 1990-07-31 | 1992-02-01 | Stephen P. Dashe | High opacity solid marking composition |
FR2673838B1 (en) | 1991-03-14 | 1995-03-03 | Oreal | COSMETIC COMPOSITIONS CONTAINING A DISPERSION OF SOLID PARTICLES WITH A SURFACE COATED WITH A CATIONIC POLYMER. |
JP3006640B2 (en) | 1992-02-05 | 2000-02-07 | 戸田工業株式会社 | Manufacturing method of granular hematite particle powder |
JP3037521B2 (en) | 1992-11-04 | 2000-04-24 | 三菱鉛筆株式会社 | Cosmetics |
US5428099A (en) * | 1993-05-19 | 1995-06-27 | Exxon Chemical Patents Inc. | Method to control carbon black distribution in elastomer blends |
JP3411342B2 (en) | 1993-08-06 | 2003-05-26 | 東京瓦斯株式会社 | Fluororesin composition containing filler or pigment |
JPH07165986A (en) | 1993-12-15 | 1995-06-27 | Tokyo Gas Co Ltd | Zinc oxide pigment for fluorine-based resin and fluorine-based resin composition |
US5501732A (en) | 1994-02-28 | 1996-03-26 | E. I. Du Pont De Nemours And Company | Process for preparing silanized TiO2 pigments using a media mill |
US5434038A (en) | 1994-03-31 | 1995-07-18 | Eastman Kodak Company | Photographic image display material |
US5482809A (en) | 1994-06-16 | 1996-01-09 | Minnesota Mining And Manufacturing Company | Liquid toners from soluble polymeric dispersants with reactive groups |
US5521271A (en) | 1994-09-29 | 1996-05-28 | Minnesota Mining And Manufacturing Company | Liquid toners with hydrocarbon solvents |
JP3653110B2 (en) | 1994-10-13 | 2005-05-25 | チタン工業株式会社 | Scale-like iron oxide pigment showing good dispersibility and dispersion stability, method for producing the same, and resin composition or organic solvent composition containing the pigment |
GB2294037B (en) | 1994-10-14 | 1998-06-24 | Tioxide Group Services Ltd | Treated titanium dioxide or zinc oxide particles |
US5558968A (en) | 1995-01-26 | 1996-09-24 | Hewlett-Packard Company | Dendrimeric toner particles for liquid electrophotography |
US5521046A (en) | 1995-03-13 | 1996-05-28 | Olin Corporation | Liquid colored toner compositions with fumed silica |
US5536615A (en) | 1995-07-05 | 1996-07-16 | Xerox Corporation | Liquid developers and toner aggregation processes |
-
1998
- 1998-07-24 US US09/122,164 patent/US6235829B1/en not_active Expired - Fee Related
-
1999
- 1999-07-22 WO PCT/GB1999/002378 patent/WO2000005313A1/en active Application Filing
- 1999-07-22 AU AU50551/99A patent/AU5055199A/en not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1514922A (en) * | 1974-06-19 | 1978-06-21 | Ici Ltd | Siliceous materials |
WO1987005924A1 (en) * | 1986-04-04 | 1987-10-08 | Revertex Limited | Dispersions of solids in organic liquids |
EP0787777A1 (en) * | 1995-06-14 | 1997-08-06 | Nippon Shokubai Co., Ltd. | Carbon black graft polymer, process for the production of the polymer and use thereof |
Cited By (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6723783B2 (en) | 2000-01-07 | 2004-04-20 | Cabot Corporation | Polymers and other groups attached to pigments and subsequent reactions |
US7893152B2 (en) | 2000-01-07 | 2011-02-22 | Cabot Corporation | Polymers and other groups attached to pigments and subsequent reactions |
WO2001051566A1 (en) * | 2000-01-07 | 2001-07-19 | Cabot Corporation | Polymers and other groups attached to pigments and subsequent reactions |
EP1134261A3 (en) * | 2000-03-16 | 2003-10-29 | Degussa AG | Carbon black |
US6555255B2 (en) * | 2000-03-24 | 2003-04-29 | World Properties, Inc. | Polymeric organic coatings and method of manufacture thereof |
GB2377819A (en) * | 2000-03-24 | 2003-01-22 | World Properties Inc | Polymeric organic coatings and method of manufacture thereof |
GB2377819B (en) * | 2000-03-24 | 2004-06-09 | World Properties Inc | Polymeric organic coatings and method of manufacture thereof |
WO2001074119A1 (en) * | 2000-03-24 | 2001-10-04 | World Properties, Inc. | Polymeric organic coatings and method of manufacture thereof |
US7794902B2 (en) | 2000-07-06 | 2010-09-14 | Cabot Corporation | Printing plates comprising modified pigment products |
WO2002004210A1 (en) * | 2000-07-06 | 2002-01-17 | Cabot Corporation | Printing plates comprising modified pigment products |
US7258956B2 (en) | 2000-07-06 | 2007-08-21 | Cabot Corporation | Printing plates comprising modified pigment products |
US6929889B2 (en) | 2000-07-06 | 2005-08-16 | Cabot Corporation | Modified pigment products, dispersions thereof, and compositions comprising the same |
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 |
US6641656B2 (en) | 2001-10-17 | 2003-11-04 | Cabot Corporation | Dispersions comprising modified pigments |
US7001934B2 (en) | 2002-01-24 | 2006-02-21 | Cabot Coroporation | Inkjet ink systems comprising a gelling agent |
US6699319B2 (en) | 2002-05-06 | 2004-03-02 | Cabot Corporation | Process for preparing modified pigments |
US6911073B2 (en) | 2002-05-06 | 2005-06-28 | Cabot Corporation | Process for preparing modified pigments |
US6916367B2 (en) | 2002-05-10 | 2005-07-12 | Cabot Corporation | Modified pigments and process for preparing modified pigments |
US6833026B2 (en) | 2002-05-10 | 2004-12-21 | Cabot Corporation | Modified pigments and process for preparing modified pigments |
US7537650B2 (en) | 2005-03-30 | 2009-05-26 | Eastman Kodak Company | Aqueous ink of colored ink and colorless ink containing anionic polymer |
US7655083B2 (en) | 2005-03-30 | 2010-02-02 | Eastman Kodak Company | Printing ink jet image with ink of cationic colorant and colorless ink of anionic polymer |
WO2010138191A1 (en) | 2009-05-29 | 2010-12-02 | Eastman Kodak Company | Aqueous compositions with improved silicon corrosion characteristics |
WO2011066117A1 (en) | 2009-11-24 | 2011-06-03 | Eastman Kodak Company | Continuous inkjet printer aquous ink composition |
WO2011066091A1 (en) | 2009-11-24 | 2011-06-03 | Eastman Kodak Company | Continuous inkjet printer aqueous ink composition |
WO2011146323A1 (en) | 2010-05-17 | 2011-11-24 | Eastman Kodak Company | Inkjet recording medium and methods therefor |
WO2012030553A2 (en) | 2010-08-31 | 2012-03-08 | Eastman Kodak Company | Recirculating fluid printing system and method |
WO2012030546A1 (en) | 2010-08-31 | 2012-03-08 | Eastman Kodak Company | Inkjet printing fluid |
WO2012087542A2 (en) | 2010-12-20 | 2012-06-28 | Eastman Kodak Company | Inkjet ink composition with jetting aid |
WO2012134783A2 (en) | 2011-03-31 | 2012-10-04 | Eastman Kodak Company | Inkjet printing ink set |
WO2012149324A1 (en) | 2011-04-29 | 2012-11-01 | Eastman Kodak Company | Recirculating inkjet printing fluid, system and method |
WO2013032826A1 (en) | 2011-08-31 | 2013-03-07 | Eastman Kodak Company | Continuous inkjet printing method and fluid set |
WO2013112440A1 (en) | 2012-01-24 | 2013-08-01 | Eastman Kodak Company | Ink having antibacterial and antifungal protection |
WO2013112400A2 (en) | 2012-01-24 | 2013-08-01 | Eastman Kodak Company | Antibacterial and antifungal protection for ink jet image |
WO2013165882A1 (en) | 2012-05-02 | 2013-11-07 | Eastman Kodak Company | Inkjet receiving medium and pre-treatment composition for inkjet printing |
WO2015199983A1 (en) | 2014-06-23 | 2015-12-30 | Eastman Kodak Company | Recirculating inkjet printing fluid |
Also Published As
Publication number | Publication date |
---|---|
AU5055199A (en) | 2000-02-14 |
US6235829B1 (en) | 2001-05-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6235829B1 (en) | Modification of chargeable pigment particles | |
Laible et al. | Formation of chemically bound polymer layers on oxide surfaces and their role in colloidal stability | |
US3532662A (en) | Process of making dispersions of pigments coated with a polymer containing polar groups in liquids | |
US5545504A (en) | Ink jettable toner compositions and processes for making and using | |
US7005225B2 (en) | Organosol including amphipathic copolymeric binder having crystalline material, and use of the organosol to make dry tones for electrographic applications | |
KR100449707B1 (en) | Liquid ink comprising surface-treated colorant and manufacturing method thereof | |
JP3774839B2 (en) | Dispersion composition and method for producing the same | |
KR100454477B1 (en) | Liquid Ink with Gel Organosol | |
US7135264B2 (en) | Organosol including amphipathic copolymeric binder and use of the organosol to make dry toners for electrographic applications | |
KR20050088342A (en) | Disperse color material and process for producing the same, water-color ink employing it, ink tank, inkjet recorder, inkjet recording method and inkjet recorded image | |
CA1290892C (en) | Process for preparing particles having monodisperse particle size | |
AU6512890A (en) | Colored metallic pigments | |
WO1991004293A9 (en) | Colored metallic pigments | |
DE602005000577T2 (en) | Process for coating particles | |
US7105263B2 (en) | Dry toner comprising encapsulated pigment, methods and uses | |
US4599291A (en) | Electrostatographic suspension developer of block copolymer reacted with mercaptan | |
US4885191A (en) | Pigment coated with polycyanoacrylate and a process for coating pigments | |
JPS6010263A (en) | Improved liquid electrophoretic developer | |
EP1621587A1 (en) | Aqueous dispersion and process for production thereof | |
US4719164A (en) | Liquid electrostatographic suspension developer comprises pigment coated with polycyanoacrylate inner shell and additional shell of copolymer | |
US4284700A (en) | Polymer coated transition metal powder as electrostatic image toner | |
US7018768B2 (en) | Organosols comprising a chromophore, methods and uses | |
EP0022639B1 (en) | Electrostatographic toner composition and electrostatographic developer composition | |
JPH06167832A (en) | Electrophotographic toner | |
JP2609153B2 (en) | Liquid developer for electrostatic photography |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT UA UG UZ VN YU ZA ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GH GM KE LS MW SD SL SZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
122 | Ep: pct application non-entry in european phase |