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US4554555A Expired / Lapsed US ⏱️ 0.0 years remaining

Recording method by use of inks

Assignee: Ricoh Co Ltd
•
Filing: 1983-12-09
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Granted: 1985-11-19
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Expires: 2003-12-09
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Abstract

Abstract A recording method by use of an ink is disclosed, in which images are formed by an aqueous ink comprising at least one dye selected from the group consisting of a pyrazolone azo dye, a phthalocyanine sulfonate dye, a xanthene dye and an azo dye on a recording medium containing at least one component selected from the group consisting of a water-soluble metal salt whose metal has an ion valence of 2 or more, an alkyl amine and a quaternary ammonium salt.

Inventors

  • 👤 Tamotsu Aruga
  • 👤 Tadashi Fujii
  • 👤 Kakuji Murakami
  • 👤 Eiichi Akutsu

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 21:14
CPC Classifications
B; B41; B41M; B41M5/00; B41M5/50; B41M5/52; B41M5/5227; B41M5/0023; C; C09; C09B; C09B11/00; C09B11/04; C09B11/10; C09B11/24; C09B63/00; C09B63/005; C09B67/00; C09B67/0071; C09B67/0072; C09B69/00; C09B69/02; C09D; C09D11/00; C09D11/30; C09D11/32; C09D11/328

Claims Analysis

Total Claims: 15
Claim 1
Independent Claim 336 words
A recording method which comprises imagewise applying (1) an aqueous ink comprising at least one dye selected from the group consisting of the following dyes (a) through (d) onto (2) a recording medium containing at least one component selected from the group consisting of water soluble metal salts in which the metal has a valence of 2 or more, alkyl amine salts, polyamines and quaternary ammonium salts, whereby to form an image on said recording medium, (a) a pyrazolone azo dye of the following formula I ##STR7## where M + represents Li + , Na + , K + , Cs + , NH 4 + or NR 4 1+ wherein R 1 represents an alkyl group, X 1 represents F, Cl, Br, I or hydrogen, and Y 1 represents hydrogen, an alkyl group or --COO--M + ; (b) a phthalocyanine sulfonate dye of the following formula II ##STR8## where M + is the same as that defined in the formula I, and m m is an integer of 2 to 4; (c) a xanthene dye of the following formula III or IV ##STR9## where M represents Li, Na, K, Cs, NH 4 or NR 4 1 wherein R 1 represents an alkyl group, X 2 represents Br, I or Cl, and Y 2 represents Br, I or Cl; ##STR10## where M is the same as that in the formula III, and R 2 represents hydrogen or an alkyl group; (d) an azo dye of the following formula V or VI ##STR11## where n is an integer of 0 or 1, X 3 represents hydrogen or --NH 2 , Y 3 represents hydrogen or --NHR 1 wherein R 1 represents an alkyl group, Z represents hydrogen, --OH or --COOM, and R 3 represents hydrogen, an alkyl group or --SO 3 M wherein M is the same as that defined in formula III; ##STR12## wherein X 4 represents hydrogen, --SO 3 M or --COOM in which M is the same as that defined in the formula III.
Claim 2
Dependent Claim 336 words
A recording method which comprises imagewise applying (1) an aqueous ink comprising at least one dye selected from the group consisting of the following dyes (a) through (d) onto (2) a recording medium containing at least one component selected from the group consisting of water soluble metal salts in which the metal has a valence of 2 or more, alkyl amine salts, polyamines and quaternary ammonium salts, whereby to form an image on said recording medium, (a) a pyrazolone azo dye of the following formula I ##STR7## where M + represents Li + , Na + , K + , Cs + , NH 4 + or NR 4 1+ wherein R 1 represents an alkyl group, X 1 represents F, Cl, Br, I or hydrogen, and Y 1 represents hydrogen, an alkyl group or --COO--M + ; (b) a phthalocyanine sulfonate dye of the following formula II ##STR8## where M + is the same as that defined in the formula I, and m m is an integer of 2 to 4; (c) a xanthene dye of the following formula III or IV ##STR9## where M represents Li, Na, K, Cs, NH 4 or NR 4 1 wherein R 1 represents an alkyl group, X 2 represents Br, I or Cl, and Y 2 represents Br, I or Cl; ##STR10## where M is the same as that in the formula III, and R 2 represents hydrogen or an alkyl group; (d) an azo dye of the following formula V or VI ##STR11## where n is an integer of 0 or 1, X 3 represents hydrogen or --NH 2 , Y 3 represents hydrogen or --NHR 1 wherein R 1 represents an alkyl group, Z represents hydrogen, --OH or --COOM, and R 3 represents hydrogen, an alkyl group or --SO 3 M wherein M is the same as that defined in formula III; ##STR12## wherein X 4 represents hydrogen, --SO 3 M or --COOM in which M is the same as that defined in the formula III.
Claim 3
Dependent Claim 59 words
A recording method as claimed in claim 1, wherein said water-soluble metal salt is selected from the group consisting of calcium chloride, calcium sulfate, calcium nitrate, magnesium chloride, magnesium sulfate, magnesium nitrate, aluminum chloride, aluminum sulfate, aluminum nitrate, barium chloride, barium nitrate, ferrous chloride, strontium chloride, strontium nitrate, stannous chloride, stannous fluoride, gallium chloride, gallium sulfate and gallium nitrate.
Claim 4
Dependent Claim 43 words
A recording method as claimed in claim 1, wherein said alkyl amine salt is selected from the group consisting of decylamine acetate, undecylamine acetate, dodecylamine acetate, tridecylamine acetate, tetradecylamine acetate, pentadecylamine acetate, hexadecylamine acetate, heptadecylamine acetate, octadecylamine acetate, nonadecylamine acetate and eicosylamine acetate.
Claim 5
Dependent Claim 46 words
A recording method as claimed in claim 1, wherein said polyamine is selected from the group consisting of polyamide polyamine resin, polyamide-polyamine-epichlorohydrin resin, and quaternary cationic bridged polymers prepared by the reaction of the acetic acid salt or hydrochloric acid salt of polydimethylaminoethyl methacrylate and epichlorohydrin.
Claim 6
Dependent Claim 37 words
A recording method as claimed in claim 1, wherein said quaternary ammonium salt is selected from the group consisting of cetyltrimethyl ammonium bromide, cetyltrimethyl ammonium chloride, alkylisoquinolium bromide, alkylisoquinolium chloride, hexadodecyltrimethyl ammonium bromide and hexadodecyltrimethyl ammonium chloride.
Claim 7
Dependent Claim 29 words
A recording method as claimed in claim 1, wherein said pyrazolone azo dye is selected from the group consisting of C.I. Acid Yellow 17 and C.I. Acid Yellow 23.
Claim 8
Dependent Claim 29 words
A recording method as claimed in claim 1, wherein said phthalocyanine sulfonate dye is selected from the group consisting of C.I. Direct Blue 87 and C.I. Acid Blue 249.
Claim 9
Dependent Claim 35 words
A recording method as claimed in claim 1, wherein said xanthene dye is selected from group consisting of C.I. Acid Red 52, C.I., Acid Red 92, C.I. Acid Red 94 and C.I. Acid Red 289.
Claim 10
Dependent Claim 36 words
A recording method as claimed in claim 1, wherein said azo dye is selected from the group consisting of C.I. Acid Red 143, C.I. Acid Red 254, C.I. Acid Red 274 and C.I. Acid Red 260.
Claim 11
Dependent Claim 26 words
A recording method as claimed in claim 2, wherein the content of said water-soluble metal salt in said recording medium is 0.2 g/m 2 or more.
Claim 12
Dependent Claim 26 words
A recording method as claimed in claim 3, wherein the content of said alkyl amine salt in said recording medium is 0.1 g/m 2 or more.
Claim 13
Dependent Claim 24 words
A recording method as claimed in claim 4, wherein the content of said polyamine in said recording medium is 0.1 g/m 2 or more.
Claim 14
Dependent Claim 26 words
A recording method as claimed in claim 5, wherein the content of said quaternary ammonium salt in said recording medium is 0.1 g/m 2 or more.
Claim 15
Dependent Claim 29 words
A recording method as claimed in claim 1 wherein said component of said recording medium is selected from the group consisting of aluminum chloride, calcium chloride and octadecylamine acetate.

References Cited (Backward Citations)

US3932695A Cited
US3870435A Cited
US3906141A Cited
US4142738A Cited
US4382262A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-11-18 1989-05-20 1989-11-19 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-11-18 1993-05-20 1993-11-19 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-11-18 1997-05-20 1997-11-19 $7700.00 Window Closed / Lapsed

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