JP2014101510A5 - - Google Patents
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- Publication number
- JP2014101510A5 JP2014101510A5 JP2013231777A JP2013231777A JP2014101510A5 JP 2014101510 A5 JP2014101510 A5 JP 2014101510A5 JP 2013231777 A JP2013231777 A JP 2013231777A JP 2013231777 A JP2013231777 A JP 2013231777A JP 2014101510 A5 JP2014101510 A5 JP 2014101510A5
- Authority
- JP
- Japan
- Prior art keywords
- ink
- present
- group
- unsubstituted
- alkylarylene
- 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.)
- Granted
Links
- -1 trans-cinnamic acid diester Chemical class 0.000 claims 20
- 125000005842 heteroatom Chemical group 0.000 claims 16
- 125000002947 alkylene group Chemical group 0.000 claims 12
- 125000000732 arylene group Chemical group 0.000 claims 12
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 8
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims 7
- 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 claims 7
- 150000002148 esters Chemical class 0.000 claims 7
- 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 claims 7
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims 5
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims 4
- 239000000178 monomer Substances 0.000 claims 4
- 235000002906 tartaric acid Nutrition 0.000 claims 4
- 239000011975 tartaric acid Substances 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 3
- 239000000155 melt Substances 0.000 claims 2
- 230000008023 solidification Effects 0.000 claims 2
- 238000007711 solidification Methods 0.000 claims 2
- ZWVMLYRJXORSEP-LURJTMIESA-N (2s)-hexane-1,2,6-triol Chemical compound OCCCC[C@H](O)CO ZWVMLYRJXORSEP-LURJTMIESA-N 0.000 claims 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 1
- XBGRWNKCSCFCAA-UHDJGPCESA-N OCC1CCC(CO)O1.OC(=O)\C=C\C1=CC=CC=C1 Chemical compound OCC1CCC(CO)O1.OC(=O)\C=C\C1=CC=CC=C1 XBGRWNKCSCFCAA-UHDJGPCESA-N 0.000 claims 1
- IOMZCYWFJSCYQN-UHDJGPCESA-N [2-(hydroxymethyl)furan-3-yl]methanol;(e)-3-phenylprop-2-enoic acid Chemical compound OCC=1C=COC=1CO.OC(=O)\C=C\C1=CC=CC=C1 IOMZCYWFJSCYQN-UHDJGPCESA-N 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 235000010290 biphenyl Nutrition 0.000 claims 1
- 239000004305 biphenyl Substances 0.000 claims 1
- 125000006267 biphenyl group Chemical group 0.000 claims 1
- 229940114081 cinnamate Drugs 0.000 claims 1
- 239000003086 colorant Substances 0.000 claims 1
- 239000000470 constituent Substances 0.000 claims 1
- 238000002425 crystallisation Methods 0.000 claims 1
- 230000008025 crystallization Effects 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- LCKIPSGLXMCAOF-HZPDHXFCSA-N dibenzyl (2r,3r)-2,3-dihydroxybutanedioate Chemical group O=C([C@H](O)[C@@H](O)C(=O)OCC=1C=CC=CC=1)OCC1=CC=CC=C1 LCKIPSGLXMCAOF-HZPDHXFCSA-N 0.000 claims 1
- UXHUJQMSTNOTRT-ZIAGYGMSSA-N dicyclohexyl (2r,3r)-2,3-dihydroxybutanedioate Chemical compound O=C([C@H](O)[C@@H](O)C(=O)OC1CCCCC1)OC1CCCCC1 UXHUJQMSTNOTRT-ZIAGYGMSSA-N 0.000 claims 1
- 150000005690 diesters Chemical class 0.000 claims 1
- 230000001747 exhibiting effect Effects 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 1
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims 1
- SMAKEJNOUFLEEJ-UHFFFAOYSA-N CCC1CCC(CC)CC1 Chemical compound CCC1CCC(CC)CC1 SMAKEJNOUFLEEJ-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/680,271 US8778069B2 (en) | 2012-11-19 | 2012-11-19 | Phase change inks containing oligomeric rosin esters |
| US13/680,271 | 2012-11-19 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014101510A JP2014101510A (ja) | 2014-06-05 |
| JP2014101510A5 true JP2014101510A5 (enExample) | 2016-12-22 |
| JP6157321B2 JP6157321B2 (ja) | 2017-07-05 |
Family
ID=50726711
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013231777A Expired - Fee Related JP6157321B2 (ja) | 2012-11-19 | 2013-11-08 | オリゴマー性ロジンエステルを含有する相変化インク |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US8778069B2 (enExample) |
| JP (1) | JP6157321B2 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9120943B2 (en) * | 2013-10-15 | 2015-09-01 | Xerox Corporation | Bio-renewable phase change inks |
| JP7093150B2 (ja) * | 2018-12-06 | 2022-06-29 | 日本化薬株式会社 | 硬化性樹脂組成物及びその硬化物 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5006170A (en) * | 1989-06-22 | 1991-04-09 | Xerox Corporation | Hot melt ink compositions |
| US5750604A (en) * | 1996-06-28 | 1998-05-12 | Tektronix, Inc. | Phase change ink formulation using a urethane isocyanate-derived resin |
| US5780528A (en) * | 1996-06-28 | 1998-07-14 | Tektronix, Inc. | Isocyanate-derived colored resins for use in phase change ink jet inks |
| US5919839A (en) * | 1996-06-28 | 1999-07-06 | Tektronix, Inc. | Phase change ink formulation using an isocyanate-derived wax and a clear ink carrier base |
| NL1012549C2 (nl) * | 1999-07-09 | 2001-01-10 | Ocu Technologies B V | Inktsamenstelling voor een smeltbare inkt en een werkwijze voor het bedrukken van een substraat met een dergelijke inktsamenstelling. |
| US20030101902A1 (en) * | 2001-12-04 | 2003-06-05 | Ann Reitnauer | Hot melt inks |
| US20080098929A1 (en) * | 2006-10-26 | 2008-05-01 | Xerox Corporation | Phase change inks |
| US20080098930A1 (en) * | 2006-11-01 | 2008-05-01 | Xerox Corporation | Colorant dispersant |
| US9499709B2 (en) * | 2010-03-01 | 2016-11-22 | Xerox Corporation | Oligomeric rosin esters for use in inks |
| US8968452B2 (en) * | 2011-04-27 | 2015-03-03 | Xerox Corporation | Phase change inks containing crystalline trans-cinnamic diesters and amorphous isosorbide oligomers |
| US8465579B2 (en) * | 2011-04-27 | 2013-06-18 | Xerox Corporation | Solid ink compositions comprising crystalline esters of tartaric acid |
| KR101318708B1 (ko) * | 2010-12-15 | 2013-10-16 | 에스케이이노베이션 주식회사 | 폴리프로필렌카보네이트를 이용한 로토그라비아 핫멜트 잉크 조성물 |
| US8906150B2 (en) * | 2011-04-27 | 2014-12-09 | Xerox Corporation | Phase change inks containing crystalline trans-cinnamic diesters and polyterpene resins |
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2012
- 2012-11-19 US US13/680,271 patent/US8778069B2/en not_active Expired - Fee Related
-
2013
- 2013-11-08 JP JP2013231777A patent/JP6157321B2/ja not_active Expired - Fee Related