GB2294939A - Hot melt ink jet printing composition comprising an oligourea - Google Patents
Hot melt ink jet printing composition comprising an oligourea Download PDFInfo
- Publication number
- GB2294939A GB2294939A GB9422477A GB9422477A GB2294939A GB 2294939 A GB2294939 A GB 2294939A GB 9422477 A GB9422477 A GB 9422477A GB 9422477 A GB9422477 A GB 9422477A GB 2294939 A GB2294939 A GB 2294939A
- Authority
- GB
- United Kingdom
- Prior art keywords
- primary
- component
- followed
- hot melt
- secondary monoamine
- 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.)
- Withdrawn
Links
- 239000012943 hotmelt Substances 0.000 title claims abstract description 15
- 239000000203 mixture Substances 0.000 title abstract description 3
- 238000007641 inkjet printing Methods 0.000 title description 7
- 238000002844 melting Methods 0.000 claims abstract description 17
- 230000008018 melting Effects 0.000 claims abstract description 17
- 150000004985 diamines Chemical class 0.000 claims abstract description 9
- 125000005442 diisocyanate group Chemical group 0.000 claims abstract description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 3
- 125000003118 aryl group Chemical group 0.000 claims abstract description 3
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000463 material Substances 0.000 claims description 11
- 239000012948 isocyanate Substances 0.000 claims description 6
- 239000003086 colorant Substances 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 abstract description 2
- 239000000976 ink Substances 0.000 description 14
- 238000000034 method Methods 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 5
- QWDQYHPOSSHSAW-UHFFFAOYSA-N 1-isocyanatooctadecane Chemical compound CCCCCCCCCCCCCCCCCCN=C=O QWDQYHPOSSHSAW-UHFFFAOYSA-N 0.000 description 4
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 2
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 1
- OHVLMTFVQDZYHP-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CN1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O OHVLMTFVQDZYHP-UHFFFAOYSA-N 0.000 description 1
- RQBUVIFBALZGPC-UHFFFAOYSA-N 1-isocyanato-4-(4-isocyanatophenyl)benzene Chemical compound C1=CC(N=C=O)=CC=C1C1=CC=C(N=C=O)C=C1 RQBUVIFBALZGPC-UHFFFAOYSA-N 0.000 description 1
- DDHUNHGZUHZNKB-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diamine Chemical compound NCC(C)(C)CN DDHUNHGZUHZNKB-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- JZUHIOJYCPIVLQ-UHFFFAOYSA-N 2-methylpentane-1,5-diamine Chemical compound NCC(C)CCCN JZUHIOJYCPIVLQ-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- CONKBQPVFMXDOV-QHCPKHFHSA-N 6-[(5S)-5-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-2-oxo-1,3-oxazolidin-3-yl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C[C@H]1CN(C(O1)=O)C1=CC2=C(NC(O2)=O)C=C1 CONKBQPVFMXDOV-QHCPKHFHSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- IXQBIOPGDNZYNA-UHFFFAOYSA-N N=C=O.N=C=O.CC1=CC=CC=C1C1=CC=CC=C1C Chemical compound N=C=O.N=C=O.CC1=CC=CC=C1C1=CC=CC=C1C IXQBIOPGDNZYNA-UHFFFAOYSA-N 0.000 description 1
- SPTUBPSDCZNVSI-UHFFFAOYSA-N N=C=O.N=C=O.COC1=CC=CC=C1C1=CC=CC=C1OC Chemical compound N=C=O.N=C=O.COC1=CC=CC=C1C1=CC=CC=C1OC SPTUBPSDCZNVSI-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- HLJDOURGTRAFHE-UHFFFAOYSA-N isocyanic acid;3,5,5-trimethylcyclohex-2-en-1-one Chemical compound N=C=O.N=C=O.CC1=CC(=O)CC(C)(C)C1 HLJDOURGTRAFHE-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- SZEGKVHRCLBFKJ-UHFFFAOYSA-N n-methyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNC SZEGKVHRCLBFKJ-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- -1 polyoxypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 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
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9422477A GB2294939A (en) | 1994-11-08 | 1994-11-08 | Hot melt ink jet printing composition comprising an oligourea |
| PCT/GB1995/002572 WO1996014364A1 (fr) | 1994-11-08 | 1995-11-01 | Impression a jets d'encre thermofusible |
| AU38103/95A AU3810395A (en) | 1994-11-08 | 1995-11-01 | Hot melt ink jet printing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9422477A GB2294939A (en) | 1994-11-08 | 1994-11-08 | Hot melt ink jet printing composition comprising an oligourea |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB9422477D0 GB9422477D0 (en) | 1995-01-04 |
| GB2294939A true GB2294939A (en) | 1996-05-15 |
Family
ID=10764041
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB9422477A Withdrawn GB2294939A (en) | 1994-11-08 | 1994-11-08 | Hot melt ink jet printing composition comprising an oligourea |
Country Status (3)
| Country | Link |
|---|---|
| AU (1) | AU3810395A (fr) |
| GB (1) | GB2294939A (fr) |
| WO (1) | WO1996014364A1 (fr) |
Cited By (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0816448A1 (fr) * | 1996-06-28 | 1998-01-07 | Tektronix, Inc. | Formulation d'encre à changement de phase en utilisant une résine d'uréthane dérivée d'isocyanate |
| 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 |
| 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 |
| US5782966A (en) * | 1996-06-28 | 1998-07-21 | Tektronix, Inc. | Isocyanate-derived materials for use in phase change ink jet inks |
| US5827918A (en) * | 1996-06-28 | 1998-10-27 | Tektronix, Inc. | Phase change ink formulation using urea and urethane isocyanate-derived resins |
| US5830942A (en) * | 1996-06-28 | 1998-11-03 | Tektronix, Inc. | Phase change ink formulation using a urethane and urethane/urea isocyanate-derived resins |
| US5994453A (en) * | 1996-06-28 | 1999-11-30 | Tektronix, Inc. | Phase change ink formulation containing a combination of a urethane resin, a mixed urethane/urea resin, a mono-amide and a polyethylene wax |
| US6015847A (en) * | 1998-02-13 | 2000-01-18 | Tektronix, Inc. | Magenta phase change ink formulation containing organic sulfonic acid |
| US6018005A (en) * | 1996-06-28 | 2000-01-25 | Tektronix, Inc. | Phase change ink formulation using urethane isocyanate-derived resins and a polyethylene wax |
| US6028138A (en) * | 1996-06-28 | 2000-02-22 | Tektronix, Inc. | Phase change ink formulation using urethane isocyanate-derived resins, a polyethylene wax and toughening agent |
| US6048925A (en) * | 1996-06-28 | 2000-04-11 | Xerox Corporation | Urethane isocyanate-derived resins for use in a phase change ink formulation |
| US6133353A (en) * | 1999-11-11 | 2000-10-17 | 3D Systems, Inc. | Phase change solid imaging material |
| US6180692B1 (en) | 1996-06-28 | 2001-01-30 | Xerox Corporation | Phase change ink formulation with organoleptic maskant additive |
| US6395811B1 (en) | 1999-11-11 | 2002-05-28 | 3D Systems, Inc. | Phase change solid imaging material |
| US6730150B1 (en) | 1996-06-28 | 2004-05-04 | Xerox Corporation | Phase change ink formulation containing a combination of a urethane resin, a mixed urethane/urearesin, a mono-amide and a polyethylene wax |
| EP1514912A2 (fr) | 2003-06-25 | 2005-03-16 | Xerox Corporation | Encres à changement de phase contenant des triamides ramifiés. |
| EP1935950A1 (fr) | 2006-12-18 | 2008-06-25 | Xerox Corporation | Encres de changement de phase contenant des éthers de dialkyle |
| EP1958993A1 (fr) | 2007-02-06 | 2008-08-20 | Xerox Corporation | Encres de changement de phase contenant des composés de colorants |
| EP1961793A1 (fr) | 2007-02-06 | 2008-08-27 | Xerox Corporation | Encres de changement de phase contenant des composés de colorants |
| EP1961794A1 (fr) | 2007-02-06 | 2008-08-27 | Xerox Corporation | Encres de changement de phase contenant des composés de colorants |
| EP2000514A1 (fr) | 2007-05-30 | 2008-12-10 | Xerox Corporation | Ensemble d'encre solide incorporant des matériaux naturellement dérivés et procédés associés |
| EP2107088A1 (fr) | 2008-04-03 | 2009-10-07 | Xerox Corporation | Encres à changement de phase contenant des cires de Fischer-Tropsch |
| EP2130879A1 (fr) | 2008-06-02 | 2009-12-09 | Xerox Corporation | Pigment par voie humide pour encre ? jet d'encre solide |
| US7749315B2 (en) | 2007-04-04 | 2010-07-06 | Xerox Corporation | Phase change inks containing colorant compounds |
| US7758268B2 (en) | 2005-12-20 | 2010-07-20 | Xerox Corporation | Hand held photochromic marking implement |
| US7811368B2 (en) | 2007-04-04 | 2010-10-12 | Xerox Corporation | Phase change inks containing colorant compounds |
| EP2253680A1 (fr) | 2009-05-18 | 2010-11-24 | Xerox Corporation | Encres de changement de phase pigmentées contenant des dispersants de sel d'ammonium quaternaire à faible poids moléculaire |
| EP2253611A1 (fr) | 2009-05-18 | 2010-11-24 | Xerox Corporation | Dispersants de sel d'ammonium quaternaire à faible poids moléculaire |
| EP2261291A1 (fr) | 2009-06-10 | 2010-12-15 | Xerox Corporation | Encres solides ou en phase avec des propriétés améliorées |
| US7997712B2 (en) | 2007-02-06 | 2011-08-16 | Xerox Corporation | Phase change inks containing colorant compounds |
| US8029861B2 (en) | 2008-09-23 | 2011-10-04 | Xerox Corporation | Ink carriers containing low viscosity functionalized waxes, phase change inks including same, and methods for making same |
| US8123344B2 (en) | 2008-08-04 | 2012-02-28 | Xerox Corporation | Ink carriers containing surface modified nanoparticles, phase change inks including same, and methods for making same |
| US8177897B2 (en) | 2008-11-17 | 2012-05-15 | Xerox Corporation | Phase change inks containing graphene-based carbon allotrope colorants |
| US8348409B2 (en) | 2008-11-17 | 2013-01-08 | Xerox Corporation | Ink jet inks containing nanodiamond black colorants |
| US8360546B2 (en) | 2010-12-22 | 2013-01-29 | Xerox Corporation | Phase change magnetic ink and process for preparing same |
| US8544999B2 (en) | 2010-12-22 | 2013-10-01 | Xerox Corporation | Phase change magnetic ink and process for preparing same |
| US8616693B1 (en) | 2012-11-30 | 2013-12-31 | Xerox Corporation | Phase change ink comprising colorants derived from plants and insects |
| US8647422B1 (en) | 2012-11-30 | 2014-02-11 | Xerox Corporation | Phase change ink comprising a modified polysaccharide composition |
| US8646896B2 (en) | 2011-03-17 | 2014-02-11 | Xerox Corporation | Phase change magnetic ink comprising surfactant coated magnetic nanoparticles and process for preparing same |
| US8657431B2 (en) | 2011-03-17 | 2014-02-25 | Xerox Corporation | Phase change magnetic ink comprising carbon coated magnetic nanoparticles and process for preparing same |
| US8696100B1 (en) | 2012-10-02 | 2014-04-15 | Xerox Corporation | Phase change ink containing synergist for pigment dispersion |
| US8702217B2 (en) | 2011-03-17 | 2014-04-22 | Xerox Corporation | Phase change magnetic ink comprising polymer coated magnetic nanoparticles and process for preparing same |
| US8714724B2 (en) | 2012-10-02 | 2014-05-06 | Xerox Corporation | Phase change inks containing novel synergist |
| US8791202B2 (en) | 2007-09-21 | 2014-07-29 | Xerox Corporation | Phase change ink compositions |
| US8911543B2 (en) | 2012-12-18 | 2014-12-16 | Xerox Corporation | Phenylcyclohexanol derivatives as wax modifiers and gelators |
| US8974047B2 (en) | 2012-11-27 | 2015-03-10 | Xerox Corporation | Phase change ink containing ethylene vinyl acetate |
| US8980406B2 (en) | 2012-08-28 | 2015-03-17 | 3D Systems, Inc. | Color stable inks and applications thereof |
| JP2015120898A (ja) * | 2013-12-06 | 2015-07-02 | ゼロックス コーポレイションＸｅｒｏｘ Ｃｏｒｐｏｒａｔｉｏｎ | 相変化インク用の非晶質材料としてのビス−尿素 |
| US9090758B2 (en) | 2012-11-30 | 2015-07-28 | Xerox Corporation | Phase change ink comprising modified naturally-derived colorants |
| US9090777B2 (en) | 2013-04-04 | 2015-07-28 | Xerox Corporation | Low cost process for solid ink using dry flushed pigments |
| US9157002B2 (en) | 2013-07-12 | 2015-10-13 | Xerox Corporation | Phase change ink pigment dispersion process |
| US9657186B2 (en) | 2012-09-13 | 2017-05-23 | 3D Systems, Inc. | Opaque inks and applications thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5006170A (en) * | 1989-06-22 | 1991-04-09 | Xerox Corporation | Hot melt ink compositions |
| JPH05255630A (ja) * | 1992-03-16 | 1993-10-05 | Ricoh Co Ltd | ホットメルトインク組成物及びこれを用いた記録方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62179580A (ja) * | 1986-01-31 | 1987-08-06 | Asahi Chem Ind Co Ltd | ワツクス状組成物 |
| GB9226772D0 (en) * | 1992-12-23 | 1993-02-17 | Coates Brothers Plc | Hot melt ink jet printing |
-
1994
- 1994-11-08 GB GB9422477A patent/GB2294939A/en not_active Withdrawn
-
1995
- 1995-11-01 AU AU38103/95A patent/AU3810395A/en not_active Abandoned
- 1995-11-01 WO PCT/GB1995/002572 patent/WO1996014364A1/fr active Application Filing
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5006170A (en) * | 1989-06-22 | 1991-04-09 | Xerox Corporation | Hot melt ink compositions |
| JPH05255630A (ja) * | 1992-03-16 | 1993-10-05 | Ricoh Co Ltd | ホットメルトインク組成物及びこれを用いた記録方法 |
Cited By (69)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7064230B2 (en) | 1996-06-28 | 2006-06-20 | Xerox Corporation | Phase change ink formulation containing a combination of a urethane resin, a mixed urethane/urearesin, a mono-amide and a polyethylene wax |
| US6180692B1 (en) | 1996-06-28 | 2001-01-30 | Xerox Corporation | Phase change ink formulation with organoleptic maskant additive |
| EP0816449A1 (fr) * | 1996-06-28 | 1998-01-07 | Tektronix, Inc. | Formulation d'encre à changement de phase en utilisant des résines d'urée et d'uréthane dérivées d'isocyanate |
| EP0816446A1 (fr) * | 1996-06-28 | 1998-01-07 | Tektronix, Inc. | Formulation d'encre à changement de phase en utilisant des résines d'uréthane et d'uréthane-urée dérivées d'isocyanate |
| EP0816445A1 (fr) * | 1996-06-28 | 1998-01-07 | Tektronix, Inc. | Matériaux à base d'isocyanate pour l'imprimante à jet d'encre à changement de phase |
| 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 |
| 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 |
| US5782966A (en) * | 1996-06-28 | 1998-07-21 | Tektronix, Inc. | Isocyanate-derived materials for use in phase change ink jet inks |
| US5827918A (en) * | 1996-06-28 | 1998-10-27 | Tektronix, Inc. | Phase change ink formulation using urea and urethane isocyanate-derived resins |
| US6303185B1 (en) | 1996-06-28 | 2001-10-16 | Xerox Corporation | Overcoating of printed substrates |
| US5994453A (en) * | 1996-06-28 | 1999-11-30 | Tektronix, Inc. | Phase change ink formulation containing a combination of a urethane resin, a mixed urethane/urea resin, a mono-amide and a polyethylene wax |
| EP0816448A1 (fr) * | 1996-06-28 | 1998-01-07 | Tektronix, Inc. | Formulation d'encre à changement de phase en utilisant une résine d'uréthane dérivée d'isocyanate |
| US6018005A (en) * | 1996-06-28 | 2000-01-25 | Tektronix, Inc. | Phase change ink formulation using urethane isocyanate-derived resins and a polyethylene wax |
| US6028138A (en) * | 1996-06-28 | 2000-02-22 | Tektronix, Inc. | Phase change ink formulation using urethane isocyanate-derived resins, a polyethylene wax and toughening agent |
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Also Published As
| Publication number | Publication date |
|---|---|
| WO1996014364A1 (fr) | 1996-05-17 |
| GB9422477D0 (en) | 1995-01-04 |
| AU3810395A (en) | 1996-05-31 |
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