RU2593865C2 - Меняющие фазовое состояние чернила, содержащие кристаллические транс-коричные сложные диэфиры и политерпеновые смолы - Google Patents
Меняющие фазовое состояние чернила, содержащие кристаллические транс-коричные сложные диэфиры и политерпеновые смолы Download PDFInfo
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- RU2593865C2 RU2593865C2 RU2012149804/05A RU2012149804A RU2593865C2 RU 2593865 C2 RU2593865 C2 RU 2593865C2 RU 2012149804/05 A RU2012149804/05 A RU 2012149804/05A RU 2012149804 A RU2012149804 A RU 2012149804A RU 2593865 C2 RU2593865 C2 RU 2593865C2
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- Prior art keywords
- esters
- trans
- aryl
- alkyl
- ink
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- PXRCIOIWVGAZEP-UHFFFAOYSA-N Primaeres Camphenhydrat Natural products C1CC2C(O)(C)C(C)(C)C1C2 PXRCIOIWVGAZEP-UHFFFAOYSA-N 0.000 claims description 6
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- ZYPYEBYNXWUCEA-UHFFFAOYSA-N camphenilone Natural products C1CC2C(=O)C(C)(C)C1C2 ZYPYEBYNXWUCEA-UHFFFAOYSA-N 0.000 claims description 6
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Classifications
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/102—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/34—Hot-melt inks
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
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Landscapes
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- Ink Jet (AREA)
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| US13/303,516 | 2011-11-23 | ||
| US13/303,516 US8906150B2 (en) | 2011-04-27 | 2011-11-23 | Phase change inks containing crystalline trans-cinnamic diesters and polyterpene resins |
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| RU2012149804A RU2012149804A (ru) | 2014-05-27 |
| RU2593865C2 true RU2593865C2 (ru) | 2016-08-10 |
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| RU2012149804/05A RU2593865C2 (ru) | 2011-11-23 | 2012-11-22 | Меняющие фазовое состояние чернила, содержащие кристаллические транс-коричные сложные диэфиры и политерпеновые смолы |
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| KR (1) | KR20130057399A (enExample) |
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| CA (1) | CA2795966C (enExample) |
| DE (1) | DE102012220354A1 (enExample) |
| RU (1) | RU2593865C2 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8841055B2 (en) * | 2012-04-04 | 2014-09-23 | Xerox Corporation | Super low melt emulsion aggregation toners comprising a trans-cinnamic di-ester |
| US8778069B2 (en) * | 2012-11-19 | 2014-07-15 | Xerox Corporation | Phase change inks containing oligomeric rosin esters |
| US9074104B2 (en) * | 2013-09-04 | 2015-07-07 | Xerox Corporation | Inks comprising amorphous ureas |
| US10081611B2 (en) * | 2014-11-21 | 2018-09-25 | Archer Daniels Midland Company | Method for acid-catalyzed acylation of the reduction products of 5-hydroxymethyl furfural |
| US9910373B2 (en) | 2015-07-17 | 2018-03-06 | Xerox Corporation | Cold pressure fix toner compositions based on small molecule crystalline and amorphous organic compound mixtures |
| JP6981972B2 (ja) | 2015-10-02 | 2021-12-17 | ザ ケマーズ カンパニー エフシー リミテッド ライアビリティ カンパニー | フッ素化表面効果コーティングにおける疎水性エクステンダー |
| CN114867607B (zh) * | 2019-12-20 | 2023-10-17 | 花王株式会社 | 喷墨墨水 |
| US20220331878A1 (en) * | 2021-04-16 | 2022-10-20 | MetalPrinting Inc. | Three-Dimensional Printing Head Device and Ink |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5173113A (en) * | 1991-03-12 | 1992-12-22 | Topez Company | Composition for ink vehicles and protective coatings |
| US5817169A (en) * | 1996-09-27 | 1998-10-06 | Xerox Corporation | Oxazoline hot melt ink compositions |
| RU2153513C2 (ru) * | 1994-07-14 | 2000-07-27 | Тоунджет Корпорейшн Пти. Лтд. | Твердые чернила для струйного принтера |
| US6306203B1 (en) * | 1999-09-23 | 2001-10-23 | Xerox Corporation | Phase change inks |
| US6797745B1 (en) * | 1999-09-23 | 2004-09-28 | Xerox Corporation | Hot melt inks containing styrene or terpene polymers |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB953427A (en) | 1959-10-02 | 1964-03-25 | Aspro Nicholas Ltd | New oxazoline derivatives and method for the preparation thereof |
| US3308024A (en) | 1959-10-02 | 1967-03-07 | Aspro Nicholas Ltd | Method of tranquilization |
| US4169836A (en) | 1974-03-27 | 1979-10-02 | Exxon Research & Engineering Co. | Oxazoline containing additive |
| US4153566A (en) | 1974-03-27 | 1979-05-08 | Exxon Research & Engineering Co. | Oxazoline additives useful in oleaginous compositions |
| CH648753A5 (de) * | 1981-07-22 | 1985-04-15 | Givaudan & Cie Sa | Lichtschutzmittel. |
| US5922117A (en) * | 1997-09-23 | 1999-07-13 | Xerox Corporation | Ink compositions containing alcohols |
| US7098163B2 (en) * | 1998-08-27 | 2006-08-29 | Cabot Corporation | Method of producing membrane electrode assemblies for use in proton exchange membrane and direct methanol fuel cells |
| JP2002317155A (ja) * | 2001-04-23 | 2002-10-31 | Nippon Kayaku Co Ltd | エネルギー線硬化型粘着剤組成物および粘着シート |
| DE602004019436D1 (de) * | 2004-12-16 | 2009-03-26 | Agfa Graphics Nv | Verfahren zum Tintenstrahldrucken mit strahlenhärtbarer Tinte bei welchem eine Flüssigkeit zur Kontrolle der Punktgrösse verwendet wird |
| EP1877464B1 (en) * | 2005-03-18 | 2015-05-27 | Battelle Memorial Institute | Resins, low temperature formulations, and coatings derived therefrom |
| US7677713B2 (en) * | 2007-05-30 | 2010-03-16 | Xerox Corporation | Solid ink set incorporating naturally derived materials and processes thereof |
| US8187780B2 (en) * | 2008-10-21 | 2012-05-29 | Xerox Corporation | Toner compositions and processes |
| US8968452B2 (en) * | 2011-04-27 | 2015-03-03 | Xerox Corporation | Phase change inks containing crystalline trans-cinnamic diesters and amorphous isosorbide oligomers |
-
2011
- 2011-11-23 US US13/303,516 patent/US8906150B2/en not_active Expired - Fee Related
-
2012
- 2012-10-29 JP JP2012237493A patent/JP5865233B2/ja not_active Expired - Fee Related
- 2012-11-08 DE DE102012220354A patent/DE102012220354A1/de not_active Ceased
- 2012-11-16 CA CA2795966A patent/CA2795966C/en not_active Expired - Fee Related
- 2012-11-21 KR KR1020120132538A patent/KR20130057399A/ko not_active Withdrawn
- 2012-11-22 RU RU2012149804/05A patent/RU2593865C2/ru not_active IP Right Cessation
- 2012-11-23 CN CN201210482868.0A patent/CN103131259B/zh not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5173113A (en) * | 1991-03-12 | 1992-12-22 | Topez Company | Composition for ink vehicles and protective coatings |
| RU2153513C2 (ru) * | 1994-07-14 | 2000-07-27 | Тоунджет Корпорейшн Пти. Лтд. | Твердые чернила для струйного принтера |
| US5817169A (en) * | 1996-09-27 | 1998-10-06 | Xerox Corporation | Oxazoline hot melt ink compositions |
| US6306203B1 (en) * | 1999-09-23 | 2001-10-23 | Xerox Corporation | Phase change inks |
| US6797745B1 (en) * | 1999-09-23 | 2004-09-28 | Xerox Corporation | Hot melt inks containing styrene or terpene polymers |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2795966C (en) | 2015-09-29 |
| DE102012220354A1 (de) | 2013-05-23 |
| US20130131226A1 (en) | 2013-05-23 |
| KR20130057399A (ko) | 2013-05-31 |
| CA2795966A1 (en) | 2013-05-23 |
| JP2013108073A (ja) | 2013-06-06 |
| RU2012149804A (ru) | 2014-05-27 |
| JP5865233B2 (ja) | 2016-02-17 |
| CN103131259A (zh) | 2013-06-05 |
| US8906150B2 (en) | 2014-12-09 |
| CN103131259B (zh) | 2016-01-20 |
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| HE9A | Changing address for correspondence with an applicant | ||
| MM4A | The patent is invalid due to non-payment of fees |
Effective date: 20181123 |