JP5667355B2 - グラフェン・ベースの炭素同素体着色剤を含む相変化インク - Google Patents
グラフェン・ベースの炭素同素体着色剤を含む相変化インク Download PDFInfo
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- JP5667355B2 JP5667355B2 JP2009256950A JP2009256950A JP5667355B2 JP 5667355 B2 JP5667355 B2 JP 5667355B2 JP 2009256950 A JP2009256950 A JP 2009256950A JP 2009256950 A JP2009256950 A JP 2009256950A JP 5667355 B2 JP5667355 B2 JP 5667355B2
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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
-
- 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
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/324—Inkjet printing inks characterised by colouring agents containing carbon black
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S977/00—Nanotechnology
- Y10S977/70—Nanostructure
- Y10S977/734—Fullerenes, i.e. graphene-based structures, such as nanohorns, nanococoons, nanoscrolls or fullerene-like structures, e.g. WS2 or MoS2 chalcogenide nanotubes, planar C3N4, etc.
- Y10S977/742—Carbon nanotubes, CNTs
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S977/00—Nanotechnology
- Y10S977/70—Nanostructure
- Y10S977/734—Fullerenes, i.e. graphene-based structures, such as nanohorns, nanococoons, nanoscrolls or fullerene-like structures, e.g. WS2 or MoS2 chalcogenide nanotubes, planar C3N4, etc.
- Y10S977/742—Carbon nanotubes, CNTs
- Y10S977/75—Single-walled
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S977/00—Nanotechnology
- Y10S977/70—Nanostructure
- Y10S977/734—Fullerenes, i.e. graphene-based structures, such as nanohorns, nanococoons, nanoscrolls or fullerene-like structures, e.g. WS2 or MoS2 chalcogenide nanotubes, planar C3N4, etc.
- Y10S977/742—Carbon nanotubes, CNTs
- Y10S977/752—Multi-walled
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S977/00—Nanotechnology
- Y10S977/902—Specified use of nanostructure
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/271950 | 2008-11-17 | ||
| US12/271,950 US8177897B2 (en) | 2008-11-17 | 2008-11-17 | Phase change inks containing graphene-based carbon allotrope colorants |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010121129A JP2010121129A (ja) | 2010-06-03 |
| JP2010121129A5 JP2010121129A5 (enExample) | 2012-11-01 |
| JP5667355B2 true JP5667355B2 (ja) | 2015-02-12 |
Family
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| Application Number | Title | Priority Date | Filing Date |
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Country Status (4)
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| US (1) | US8177897B2 (enExample) |
| JP (1) | JP5667355B2 (enExample) |
| KR (1) | KR101518070B1 (enExample) |
| CN (1) | CN101735685B (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8460451B2 (en) * | 2011-02-23 | 2013-06-11 | 3D Systems, Inc. | Support material and applications thereof |
| US8431217B2 (en) | 2011-09-12 | 2013-04-30 | Xerox Corporation | Core-shell particles and fuser member made therefrom |
| US9452608B2 (en) * | 2012-05-09 | 2016-09-27 | Canon Kabushiki Kaisha | Ink, ink cartridge and ink jet recording method |
| WO2013176494A1 (ko) | 2012-05-23 | 2013-11-28 | 주식회사 엘지화학 | 상변이 잉크 조성물 및 이를 이용한 전도성 패턴 |
| GB201218952D0 (en) * | 2012-10-22 | 2012-12-05 | Cambridge Entpr Ltd | Functional inks based on layered materials and printed layered materials |
| US9302945B2 (en) | 2014-03-07 | 2016-04-05 | Lockheed Martin Corporation | 3-D diamond printing using a pre-ceramic polymer with a nanoparticle filler |
| US9315685B2 (en) * | 2014-04-19 | 2016-04-19 | Xerox Corporation | Process for preparing an aqueous ink jet printing ink |
| US9504158B2 (en) | 2014-04-22 | 2016-11-22 | Facebook, Inc. | Metal-free monolithic epitaxial graphene-on-diamond PWB |
| US9402322B1 (en) | 2015-03-04 | 2016-07-26 | Lockheed Martin Corporation | Metal-free monolithic epitaxial graphene-on-diamond PWB with optical waveguide |
| CN105086631A (zh) * | 2015-09-06 | 2015-11-25 | 江南大学 | 光敏碳纳米管的制备方法及紫外光固化导电油墨 |
| CN108795107A (zh) * | 2018-03-24 | 2018-11-13 | 成都迪泰化工有限公司 | 一种石墨烯的改性方法及其产物和uv光固化涂料 |
| CN111647322B (zh) * | 2020-06-27 | 2022-07-22 | 德阳聪源光电科技股份有限公司 | 用于制备柔性发热膜的导电油墨组合物 |
| US12441904B2 (en) | 2020-10-13 | 2025-10-14 | Chasm Advanced Materials, Inc. | Curable carbon nanotube ink and transparent conductive films created using the ink |
| KR20230087579A (ko) * | 2020-10-13 | 2023-06-16 | 캐즘 어드밴스드 머티리얼스, 인크. | 경화성 탄소 나노튜브 잉크 및 잉크를 사용하여 생성된 투명 전도성 필름 |
| US12428301B1 (en) | 2021-03-26 | 2025-09-30 | Alvin T. Rockhill | Graphene composition |
| EP4488341A1 (en) * | 2023-07-05 | 2025-01-08 | Canon Production Printing Holding B.V. | Radiation-curable ink composition, method for preparing the same and method for applying an image onto a recording medium |
| CN117186700B (zh) * | 2023-09-08 | 2025-07-18 | 广州市嵩达新材料科技有限公司 | 一种喷墨打印导电墨水及其制备方法与应用 |
Family Cites Families (77)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1248643B (de) | 1959-03-30 | 1967-08-31 | The Lubrizol Corporation, Cleveland, Ohio (V. St. A.) | Verfahren zur Herstellung von öllöslichen aeylierten Aminen |
| NL124842C (enExample) | 1959-08-24 | |||
| US3381022A (en) | 1963-04-23 | 1968-04-30 | Lubrizol Corp | Polymerized olefin substituted succinic acid esters |
| US3280034A (en) | 1963-07-22 | 1966-10-18 | Monsanto Co | Alkenylsuccinimido alkyl-substituted imidazolidines and related materials |
| US3442808A (en) | 1966-11-01 | 1969-05-06 | Standard Oil Co | Lubricating oil additives |
| BE755392A (fr) | 1969-08-28 | 1971-02-01 | Teletype Corp | Encre et appareil d'impression electrostatique |
| US3996059A (en) | 1971-12-30 | 1976-12-07 | Imperial Chemical Industries Limited | Dispersing agents |
| US3912764A (en) | 1972-09-29 | 1975-10-14 | Cooper Edwin Inc | Preparation of alkenyl succinic anhydrides |
| US4234435A (en) | 1979-02-23 | 1980-11-18 | The Lubrizol Corporation | Novel carboxylic acid acylating agents, derivatives thereof, concentrate and lubricant compositions containing the same, and processes for their preparation |
| US4390369A (en) | 1981-12-17 | 1983-06-28 | Exxon Research And Engineering Co. | Natural wax-containing ink jet inks |
| US4484948A (en) | 1981-12-17 | 1984-11-27 | Exxon Research And Engineering Co. | Natural wax-containing ink jet inks |
| DE3579067D1 (de) | 1984-05-10 | 1990-09-13 | Willett Int Ltd | Verfahren zur beschichtung eines substrates mit thermoplastischen ttinten, und beschichtungszusammensetzung. |
| US5165909A (en) | 1984-12-06 | 1992-11-24 | Hyperion Catalysis Int'l., Inc. | Carbon fibrils and method for producing same |
| DE3583130D1 (de) | 1984-12-31 | 1991-07-11 | Howtek Inc | Verfahren zum farbdrucken mit tintenstrahl. |
| JPS6354476A (ja) | 1986-08-25 | 1988-03-08 | Seiko Epson Corp | 熱溶融性インク |
| US5194638A (en) | 1987-09-18 | 1993-03-16 | Union Camp Corporation | Resinous binders for use in ink compositions for ink jet printing |
| US4830671A (en) | 1987-09-18 | 1989-05-16 | Union Camp Corporation | Ink compositions for ink jet printing |
| US4889560A (en) | 1988-08-03 | 1989-12-26 | Tektronix, Inc. | Phase change ink composition and phase change ink produced therefrom |
| US4889761A (en) | 1988-08-25 | 1989-12-26 | Tektronix, Inc. | Substrates having a light-transmissive phase change ink printed thereon and methods for producing same |
| US5151120A (en) | 1989-03-31 | 1992-09-29 | Hewlett-Packard Company | Solid ink compositions for thermal ink-jet printing having improved printing characteristics |
| US5195430A (en) | 1989-05-24 | 1993-03-23 | Tektronix, Inc. | Dual roller apparatus for pressure fixing sheet material |
| US5006170A (en) | 1989-06-22 | 1991-04-09 | Xerox Corporation | Hot melt ink compositions |
| GB2238792A (en) | 1989-09-07 | 1991-06-12 | Coates Brothers Plc | Polyamides |
| US5221335A (en) | 1990-05-23 | 1993-06-22 | Coates Electrographics Limited | Stabilized pigmented hot melt ink containing nitrogen-modified acrylate polymer as dispersion-stabilizer agent |
| DE4205713C2 (de) | 1992-02-25 | 1994-08-04 | Siegwerk Druckfarben Gmbh & Co | Druckfarbe, Verfahren zu ihrer Herstellung und deren Verwendung |
| US5319030A (en) | 1992-07-23 | 1994-06-07 | Chevron Research And Technology Company | One-step process for the preparation of alkenyl succinic anhydride |
| US5286799A (en) | 1992-07-23 | 1994-02-15 | Chevron Research And Technology Company | Two-step free radical catalyzed process for the preparation of alkenyl succinic anhydride |
| US5385957A (en) | 1992-08-24 | 1995-01-31 | Videojet Systems International, Inc. | Hotmelt ink jet comprising ionomers having melting points from about 50° C. to about 130° or a softening point below about 80° C., and an image-forming agent |
| US5372852A (en) | 1992-11-25 | 1994-12-13 | Tektronix, Inc. | Indirect printing process for applying selective phase change ink compositions to substrates |
| US5389958A (en) | 1992-11-25 | 1995-02-14 | Tektronix, Inc. | Imaging process |
| GB9226772D0 (en) | 1992-12-23 | 1993-02-17 | Coates Brothers Plc | Hot melt ink jet printing |
| GB2280905A (en) | 1993-08-06 | 1995-02-15 | Coates Brothers Plc | Ethylenically unsaturated photoinitiator |
| GB2290793B (en) | 1994-06-20 | 1998-05-06 | Cray Valley Ltd | Powder coating compositions |
| GB2294939A (en) | 1994-11-08 | 1996-05-15 | Coates Brothers Plc | Hot melt ink jet printing composition comprising an oligourea |
| GB2305670A (en) | 1995-09-27 | 1997-04-16 | Coates Brothers Plc | Hot melt ink jet vehicles |
| GB2305928A (en) | 1995-10-06 | 1997-04-23 | Coates Brothers Plc | Coloured hot melt ink jet vehicle |
| US5821205A (en) | 1995-12-01 | 1998-10-13 | Chevron Chemical Company | Polyalkylene succinimides and post-treated derivatives thereof |
| GB9605399D0 (en) | 1996-03-14 | 1996-05-15 | Coates Brothers Plc | Hot melt ink composition |
| US5780528A (en) | 1996-06-28 | 1998-07-14 | Tektronix, Inc. | Isocyanate-derived colored resins for use in phase change ink jet inks |
| US5830942A (en) | 1996-06-28 | 1998-11-03 | Tektronix, Inc. | Phase change ink formulation using a urethane and urethane/urea isocyanate-derived resins |
| US5782966A (en) | 1996-06-28 | 1998-07-21 | Tektronix, Inc. | Isocyanate-derived materials 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 |
| US5783658A (en) | 1996-06-28 | 1998-07-21 | Tektronix, Inc. | Phase change ink formulation using a urethane isocyanate-derived resin and a urethane isocyanate-derived wax |
| US5827918A (en) | 1996-06-28 | 1998-10-27 | Tektronix, Inc. | Phase change ink formulation using urea and urethane isocyanate-derived resins |
| US5750604A (en) | 1996-06-28 | 1998-05-12 | Tektronix, Inc. | Phase change ink formulation using a urethane isocyanate-derived resin |
| AU3471099A (en) * | 1998-04-03 | 1999-10-25 | Cabot Corporation | Modified pigments having improved dispersing properties |
| US6174937B1 (en) | 1999-07-16 | 2001-01-16 | Xerox Corporation | Composition of matter, a phase change ink, and a method of reducing a coefficient of friction of a phase change ink formulation |
| US6309453B1 (en) | 1999-09-20 | 2001-10-30 | Xerox Corporation | Colorless compounds, solid inks, and printing methods |
| US6972304B2 (en) * | 2001-09-07 | 2005-12-06 | Xerox Corporation | Aqueous ink compositions |
| US6906118B2 (en) | 2001-09-07 | 2005-06-14 | Xerox Corporation | Phase change ink compositions |
| AU2002336675C1 (en) | 2001-10-29 | 2008-10-16 | Hyperion Catalysis International, Inc. | Polymer containing functionalized carbon nanotubes |
| US6841590B2 (en) | 2001-12-28 | 2005-01-11 | Sun Chemical Corporation | Hot melt flexographic inks and method of preparing same |
| US6702884B2 (en) | 2001-12-31 | 2004-03-09 | Markem Corporation | Pigmented hot melt inks |
| US6872243B2 (en) | 2002-09-04 | 2005-03-29 | Xerox Corporation | Phase change inks containing gelator additives |
| US6860928B2 (en) | 2002-09-04 | 2005-03-01 | Xerox Corporation | Alkylated urea and triaminotriazine compounds and phase change inks containing same |
| US6811595B2 (en) | 2002-09-04 | 2004-11-02 | Xerox Corporation | Guanidinopyrimidinone compounds and phase change inks containing same |
| US6761758B2 (en) | 2002-09-04 | 2004-07-13 | Xerox Corporation | Alkylated tetrakis(triaminotriazine) compounds and phase change inks containing same |
| US6923533B2 (en) * | 2002-12-09 | 2005-08-02 | Xerox Corporation | Phase change ink imaging component with nano-size filler |
| US6860930B2 (en) | 2003-06-25 | 2005-03-01 | Xerox Corporation | Phase change inks containing branched triamides |
| US6835238B1 (en) * | 2003-06-26 | 2004-12-28 | Xerox Corporation | Phase change inks containing colorant compounds |
| US7097788B2 (en) | 2003-06-30 | 2006-08-29 | The Board Of Trustees Of The University Of Illinois | Conducting inks |
| US6858070B1 (en) | 2003-11-25 | 2005-02-22 | Xerox Corporation | Phase change inks |
| JP4501445B2 (ja) * | 2004-02-06 | 2010-07-14 | 東洋インキ製造株式会社 | カーボンナノチューブ組成物、およびそれを含有するカーボンナノチューブ分散液 |
| US20050196336A1 (en) | 2004-03-05 | 2005-09-08 | Chatterjee Arup K. | Activated graphitic carbon and metal hybrids thereof |
| US20060112858A1 (en) * | 2004-11-12 | 2006-06-01 | Saigon Hi Tech Park | Liquid nano carbon and application products |
| US7220300B2 (en) | 2004-12-04 | 2007-05-22 | Xerox Corporation | Phase change inks containing bis(urea-urethane) compounds |
| US7144450B2 (en) | 2004-12-04 | 2006-12-05 | Xerox Corporation | Phase change inks containing trans-1,2-cyclohexane bis(urea-urethane) compounds |
| US7314949B2 (en) | 2004-12-04 | 2008-01-01 | Xerox Corporation | Trans-1,2-cyclohexane bis(urea-urethane) compounds |
| US7381254B2 (en) | 2005-11-30 | 2008-06-03 | Xerox Corporation | Phase change inks |
| US7714040B2 (en) | 2005-11-30 | 2010-05-11 | Xerox Corporation | Phase change inks containing curable amide gellant compounds |
| US7625956B2 (en) | 2005-11-30 | 2009-12-01 | Xerox Corporation | Phase change inks containing photoinitiator with phase change properties and gellant affinity |
| US7279587B2 (en) | 2005-11-30 | 2007-10-09 | Xerox Corporation | Photoinitiator with phase change properties and gellant affinity |
| US7259275B2 (en) | 2005-11-30 | 2007-08-21 | Xerox Corporation | Method for preparing curable amide gellant compounds |
| JP2008004800A (ja) * | 2006-06-23 | 2008-01-10 | Fujifilm Corp | 回路基板の製造方法及び回路基板 |
| US20080098930A1 (en) * | 2006-11-01 | 2008-05-01 | Xerox Corporation | Colorant dispersant |
| US8962736B2 (en) * | 2007-12-20 | 2015-02-24 | Xerox Corporation | Electrically resistive coatings/layers using soluble carbon nanotube complexes in polymers |
| JPWO2009102077A1 (ja) * | 2008-02-11 | 2011-06-16 | 国立大学法人 東京大学 | カーボンナノチューブゴム組成物、配線、導電性ペースト、電子回路およびその製造方法 |
-
2008
- 2008-11-17 US US12/271,950 patent/US8177897B2/en not_active Expired - Fee Related
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2009
- 2009-11-10 JP JP2009256950A patent/JP5667355B2/ja not_active Expired - Fee Related
- 2009-11-16 CN CN2009101801773A patent/CN101735685B/zh not_active Expired - Fee Related
- 2009-11-16 KR KR1020090110190A patent/KR101518070B1/ko not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2010121129A (ja) | 2010-06-03 |
| US8177897B2 (en) | 2012-05-15 |
| CN101735685B (zh) | 2013-09-25 |
| KR20100055339A (ko) | 2010-05-26 |
| KR101518070B1 (ko) | 2015-05-07 |
| CN101735685A (zh) | 2010-06-16 |
| US20100124611A1 (en) | 2010-05-20 |
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