NO318990B1 - Fremgangsmate for fremstilling av deodorisert harpiks for torrfarge - Google Patents
Fremgangsmate for fremstilling av deodorisert harpiks for torrfarge Download PDFInfo
- Publication number
- NO318990B1 NO318990B1 NO19965626A NO965626A NO318990B1 NO 318990 B1 NO318990 B1 NO 318990B1 NO 19965626 A NO19965626 A NO 19965626A NO 965626 A NO965626 A NO 965626A NO 318990 B1 NO318990 B1 NO 318990B1
- Authority
- NO
- Norway
- Prior art keywords
- molecular weight
- latex
- weight
- parts
- acrylate
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 37
- 229920005989 resin Polymers 0.000 title claims description 22
- 239000011347 resin Substances 0.000 title claims description 22
- 238000002360 preparation method Methods 0.000 title claims description 7
- 239000004816 latex Substances 0.000 claims description 54
- 229920000126 latex Polymers 0.000 claims description 54
- 239000000178 monomer Substances 0.000 claims description 34
- 239000000203 mixture Substances 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 20
- 230000001105 regulatory effect Effects 0.000 claims description 20
- 239000003999 initiator Substances 0.000 claims description 17
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 15
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 claims description 13
- JXXRCDTYFYLOQH-UHFFFAOYSA-N OO.C(C)(C)C(C1=CC=CC=C1)C(C)C Chemical compound OO.C(C)(C)C(C1=CC=CC=C1)C(C)C JXXRCDTYFYLOQH-UHFFFAOYSA-N 0.000 claims description 12
- 238000006116 polymerization reaction Methods 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 10
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 9
- 238000009826 distribution Methods 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- 229920002554 vinyl polymer Polymers 0.000 claims description 7
- 230000002902 bimodal effect Effects 0.000 claims description 6
- 239000003995 emulsifying agent Substances 0.000 claims description 6
- 150000002978 peroxides Chemical class 0.000 claims description 6
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 claims description 4
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims description 4
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical group COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 claims description 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 4
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 4
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 claims description 4
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 claims description 2
- BTOVVHWKPVSLBI-UHFFFAOYSA-N 2-methylprop-1-enylbenzene Chemical compound CC(C)=CC1=CC=CC=C1 BTOVVHWKPVSLBI-UHFFFAOYSA-N 0.000 claims description 2
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 claims description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 claims description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims description 2
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 claims description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 13
- 239000000975 dye Substances 0.000 description 10
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 6
- 230000035943 smell Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 4
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 4
- -1 alkyl allyl sulfonic acid Chemical compound 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
- 239000004159 Potassium persulphate Substances 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 235000019394 potassium persulphate Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 229920006164 aromatic vinyl copolymer Polymers 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000002897 diene group Chemical group 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000006385 ozonation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229940096992 potassium oleate Drugs 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- FZYCEURIEDTWNS-UHFFFAOYSA-N prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=CC=C1.CC(=C)C1=CC=CC=C1 FZYCEURIEDTWNS-UHFFFAOYSA-N 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 238000004260 weight control Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
- G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/08706—Polymers of alkenyl-aromatic compounds
- G03G9/08708—Copolymers of styrene
- G03G9/08711—Copolymers of styrene with esters of acrylic or methacrylic acid
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F6/00—Post-polymerisation treatments
- C08F6/14—Treatment of polymer emulsions
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
- G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Developing Agents For Electrophotography (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Polyesters Or Polycarbonates (AREA)
- Polymerisation Methods In General (AREA)
- Polymerization Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1019950010694A KR0145949B1 (ko) | 1995-05-02 | 1995-05-02 | 탈취된 건식 토너용 수지의 제조방법 |
| PCT/KR1996/000065 WO1996035148A1 (fr) | 1995-05-02 | 1996-05-02 | Procede de preparation d'une resine desodorisee pour poudre de toner |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO965626D0 NO965626D0 (no) | 1996-12-30 |
| NO965626L NO965626L (no) | 1997-02-13 |
| NO318990B1 true NO318990B1 (no) | 2005-05-30 |
Family
ID=19413561
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19965626A NO318990B1 (no) | 1995-05-02 | 1996-12-30 | Fremgangsmate for fremstilling av deodorisert harpiks for torrfarge |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US5852147A (fr) |
| EP (1) | EP0769164B1 (fr) |
| JP (1) | JP2777676B2 (fr) |
| KR (1) | KR0145949B1 (fr) |
| AT (1) | ATE182991T1 (fr) |
| AU (1) | AU678945B2 (fr) |
| BR (1) | BR9606353A (fr) |
| CA (1) | CA2194213C (fr) |
| DE (1) | DE69603562T2 (fr) |
| ES (1) | ES2136987T3 (fr) |
| FI (1) | FI117756B (fr) |
| NO (1) | NO318990B1 (fr) |
| WO (1) | WO1996035148A1 (fr) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3576374B2 (ja) * | 1998-03-18 | 2004-10-13 | 日本カーバイド工業株式会社 | 静電荷像現像用トナーの製造方法 |
| US6258504B1 (en) | 1999-10-13 | 2001-07-10 | Nashua Corporation | Toner containing resin prepared by a combination of emulsion followed by suspension polymerization |
| KR100368203B1 (ko) * | 2000-07-11 | 2003-01-24 | (주)거명 | 토너 바인더 수지 조성물의 제조방법 |
| US6673892B2 (en) | 2002-04-29 | 2004-01-06 | Eastman Chemical Company | Process for reducing residual free radical polymerizable monomer content of polymers |
| US7282552B1 (en) * | 2006-05-16 | 2007-10-16 | Fina Technology, Inc. | Styrene copolymers with a bimodal molecular weight distribution |
| CN101548244B (zh) * | 2006-12-19 | 2011-10-05 | 第一毛织株式会社 | 调色剂及其制备方法 |
| GB0721065D0 (en) * | 2007-10-26 | 2007-12-05 | Fujifilm Imaging Colorants Ltd | Improvements in and relating to toners made from latexes |
| CN104418959B (zh) * | 2013-08-23 | 2016-10-19 | 中国石油化工集团公司 | 一种vae乳液中有机挥发份的处理方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1231013B (de) * | 1964-07-25 | 1966-12-22 | Roehm & Haas Gmbh | Verfahren zur Herstellung von Copolymerisaten |
| US3928498A (en) * | 1973-07-05 | 1975-12-23 | Phillips Petroleum Co | Preformed polymer latex in emulsion polymerization systems |
| GB1594863A (en) * | 1978-03-03 | 1981-08-05 | Int Synthetic Rubber | Emulsion polymerisation process |
| DE3612773A1 (de) * | 1986-04-16 | 1987-10-22 | Roehm Gmbh | Verfahren zur herstellung waermeformbestaendiger formmassen |
| JPH01215846A (ja) * | 1988-02-24 | 1989-08-29 | Mitsubishi Rayon Co Ltd | 塩化ビニル系樹脂組成物 |
| JPH04330459A (ja) * | 1991-05-02 | 1992-11-18 | Konica Corp | トナーおよび画像形成方法 |
| JP3066470B2 (ja) * | 1991-05-08 | 2000-07-17 | 日本エイアンドエル株式会社 | 共重合体ラテックスの製造方法 |
| JP3078629B2 (ja) * | 1991-11-11 | 2000-08-21 | 電気化学工業株式会社 | ゴム変性スチレン−アクリル系樹脂組成物 |
| US5521268A (en) * | 1995-03-29 | 1996-05-28 | Eastman Kodak Company | Odor reduction in toner polymers |
-
1995
- 1995-05-02 KR KR1019950010694A patent/KR0145949B1/ko not_active IP Right Cessation
-
1996
- 1996-05-02 EP EP96912321A patent/EP0769164B1/fr not_active Expired - Lifetime
- 1996-05-02 WO PCT/KR1996/000065 patent/WO1996035148A1/fr active IP Right Grant
- 1996-05-02 AU AU55169/96A patent/AU678945B2/en not_active Ceased
- 1996-05-02 DE DE69603562T patent/DE69603562T2/de not_active Expired - Fee Related
- 1996-05-02 AT AT96912321T patent/ATE182991T1/de active
- 1996-05-02 CA CA002194213A patent/CA2194213C/fr not_active Expired - Fee Related
- 1996-05-02 ES ES96912321T patent/ES2136987T3/es not_active Expired - Lifetime
- 1996-05-02 US US08/765,022 patent/US5852147A/en not_active Expired - Lifetime
- 1996-05-02 JP JP8533192A patent/JP2777676B2/ja not_active Expired - Fee Related
- 1996-05-02 BR BR9606353A patent/BR9606353A/pt not_active IP Right Cessation
- 1996-12-30 NO NO19965626A patent/NO318990B1/no unknown
- 1996-12-31 FI FI965295A patent/FI117756B/fi active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| US5852147A (en) | 1998-12-22 |
| ATE182991T1 (de) | 1999-08-15 |
| NO965626L (no) | 1997-02-13 |
| BR9606353A (pt) | 1997-11-25 |
| FI965295A (fi) | 1997-02-27 |
| ES2136987T3 (es) | 1999-12-01 |
| CA2194213A1 (fr) | 1996-11-07 |
| EP0769164B1 (fr) | 1999-08-04 |
| CA2194213C (fr) | 2000-02-01 |
| JP2777676B2 (ja) | 1998-07-23 |
| NO965626D0 (no) | 1996-12-30 |
| KR0145949B1 (ko) | 1998-12-01 |
| FI117756B (fi) | 2007-02-15 |
| AU678945B2 (en) | 1997-06-12 |
| JPH09510752A (ja) | 1997-10-28 |
| DE69603562D1 (de) | 1999-09-09 |
| EP0769164A1 (fr) | 1997-04-23 |
| DE69603562T2 (de) | 2000-02-17 |
| FI965295A0 (fi) | 1996-12-31 |
| KR960042237A (ko) | 1996-12-21 |
| WO1996035148A1 (fr) | 1996-11-07 |
| AU5516996A (en) | 1996-11-21 |
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