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US3905949A Expired / Lapsed US ⏱️ 0.0 years remaining

Stilbene azo lithium salt dyes

Assignee: EIDP Inc
•
Filing: 1969-08-01
•
Granted: 1975-09-16
•
Expires: 1989-08-01
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Abstract

Abstract Stilbene azo dyes, as lithium salts or mixed lithium and sodium salts wherein the ratio of lithium to sodium is at least 1:2, especially useful for dyeing paper or paper pulp, prepared by condensing a member of the group consisting of the lithium salt of 5-nitro-o-toluenesulfonic acid and the dilithium, monolithium monosodium, and disodium salts of 4,4''-dinitro-2,2''stilbenedisulfonic acid, in an aqueous alkaline medium, at a temperature of from about 20*C. to the boiling temperature of the reaction medium, in the presence of sufficient ionic lithium to provide a ratio of lithium to sodium in the dye of at least 1:2 until formation of said stilbene azo dye is substantially complete, the condensation reaction product optionally being reacted with a reducing agent selected from the group consisting of aliphatic aldehydes, hydroxyaliphatic aldehydes, glycerol, alkanolamines, alkali metal sulfites and alkali metal sulfides to achieve shade variation.

Inventors

  • 👤 Melvin A Perkins
  • 👤 Howard K Urion

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 00:39
CPC Classifications
D; D21; D21H; D21H21/00; D21H21/14; D21H21/28; C; C09; C09B; C09B56/00; C09B56/04; C09B56/06; C09B69/00; C09B69/02

Claims Analysis

Total Claims: 16
Claim 1
Independent Claim 103 words
STILBENE AZO DYE, AS LITHIUM SALT OR MIXED LITHIUM AND SODIUM SALTS WHEREIN THE RATIO OF LITHIUM TO SODIUM IS AT LEAST 1:2 PREPARED BY CONDENSING A MEMBER OF THE GROUP CONSISTING OF THE LITHIUM SALTS OF 5-NITRO-O-TOLUENSULFONIC ACID AND THE DILITHIUM, MONOLITHIUM MONOSODIUM, AND DISODIUM SALTS OF 4,4''-DINITO-2,2''-STILBENEDISULFONIC ACID, IN AN AQUEOUS ALKALINE REACTION MEDIUM, AT A TEMPERATURE OF FROM ABOUT 20*C. TO THE BOILING TEMPERATURE OF THE REACTION MEDIUM, IN THE PRESENCE OF SULFICIENT IONIC LITHIUM TO PROVIDE A RATIO OF LITHIUM TO SODIUM IN THE DYE OF AT LEAST 1:2, UNTIL FORMATION OF SAID STILBENE AZO DYE IS SUBSTANTIALLY COMPLETE.
Claim 2
Dependent Claim 103 words
STILBENE AZO DYE, AS LITHIUM SALT OR MIXED LITHIUM AND SODIUM SALTS WHEREIN THE RATIO OF LITHIUM TO SODIUM IS AT LEAST 1:2 PREPARED BY CONDENSING A MEMBER OF THE GROUP CONSISTING OF THE LITHIUM SALTS OF 5-NITRO-O-TOLUENSULFONIC ACID AND THE DILITHIUM, MONOLITHIUM MONOSODIUM, AND DISODIUM SALTS OF 4,4''-DINITO-2,2''-STILBENEDISULFONIC ACID, IN AN AQUEOUS ALKALINE REACTION MEDIUM, AT A TEMPERATURE OF FROM ABOUT 20*C. TO THE BOILING TEMPERATURE OF THE REACTION MEDIUM, IN THE PRESENCE OF SULFICIENT IONIC LITHIUM TO PROVIDE A RATIO OF LITHIUM TO SODIUM IN THE DYE OF AT LEAST 1:2, UNTIL FORMATION OF SAID STILBENE AZO DYE IS SUBSTANTIALLY COMPLETE.
Claim 3
Dependent Claim 91 words
Stilbene azo dye of claim 1, prepared by condensing the lithium salt of 5-nitro-o-toluenesulfonic acid, in an aqueous reaction medium, in the presence of at least about 0.2 mole, per mole of lithium salt, of a base selected from lithium hydroxide and sodium hydroxide, at a temperature of from about 20*C. to the boiling temperature of the reaction medium, in the presence of sufficient ionic lithium to provide a ratio of lithium to sodium in the dye of at least 1:2, until formation of said stilbene azo dye is substantially complete.
Claim 4
Dependent Claim 121 words
Stilbene azo dye of claim 1, prepared by condensing, in admixture at a weight ratio of 70:30 to 90:10, the lithium salt of 5-nitro-o-toluenesulfonic acid and a member of the group consisting of the dilithium, monolithium monosodium, and disodium salts of 4,4''-dinitro-2,2''-stilbenedisulfonic acid, in an aqueous reaction medium, in the presence of at least about 0.2 mole, per mole of salts in the mixture, of a base selected from lithium hydroxide and sodium hydroxide, at a temperature of from about 20*C. to the boiling temperature of the reaction medium, in the presence of sufficient ionic lithium to provide a ratio of lithium to sodium in the dye of at least 1:2, until formation of said stilbene azo dye is substantially complete.
Claim 5
Dependent Claim 101 words
Stilbene azo dye of claim 1, prepared by condensing a member of the group consisting of the dilithium and monolithium monosodium salts of 4,4''-dinitro-2,2''-stilbenedisulfonic acid, in an aqueous reaction medium, in the presence of at least about 0.2 mole, per mole of stilbene salt, of a base selected from lithium hydroxide and sodium hydroxide, at a temperature of from about 20*C. to the boiling temperature of the reaction medium, in the presence of sufficient ionic lithium to provide a ratio of lithium to sodium in the dye of at least 1:2, until formation of said stilbene azo dye is substantially complete.
Claim 6
Dependent Claim 103 words
Stilbene azo dye, as lithium salt or mixed lithium and sodium salts wherein the ratio of lithium to sodium is at least 1:2, prepared by condensing a member of the group consisting of the lithium salt of 5-nitro-o-toluenesulfonic acid and the dilithium, monolithium monosodium, and disodium salts of 4,4''-dinitro-2,2''-stilbenedisulfonic acid, in an aqueous alkaline reaction medium, at a temperature of from about 20*C. to the boiling temperature of the reaction medium, in the presence of sufficient ionic lithium to provide a ratio of lithium to sodium in the dye of at least 1:2, and thereafter reacting the condensation product with a reducing agent.
Claim 7
Dependent Claim 103 words
Stilbene azo dye, as lithium salt or mixed lithium and sodium salts wherein the ratio of lithium to sodium is at least 1:2, prepared by condensing a member of the group consisting of the lithium salt of 5-nitro-o-toluenesulfonic acid and the dilithium, monolithium monosodium, and disodium salts of 4,4''-dinitro-2,2''-stilbenedisulfonic acid, in an aqueous alkaline reaction medium, at a temperature of from about 20*C. to the boiling temperature of the reaction medium, in the presence of sufficient ionic lithium to provide a ratio of lithium to sodium in the dye of at least 1:2, and thereafter reacting the condensation product with a reducing agent.
Claim 8
Dependent Claim 90 words
Stilbene azo dye of claim 5, prepared by condensing the lithium salt of 5-nitro-o-toluenesulfonic acid, in an aqueous reaction medium, in the presence of at least 0.2 mole, per mole of lithium salt, of a base selected from lithium hydroxide and sodium hydroxide, at a temperature of from about 20*C. to the boiling temperature of the reaction medium, in the presence of sufficient ionic lithium to provide a ratio of lithium to sodium in the dye of at least 1:2, and thereafter reacting the condensation product with a reducing agent.
Claim 9
Dependent Claim 122 words
Stilbene azo dye of claim 5, prepared by condensing, in admixture at a weight ratio of 70:30 to 90:10, the lithium salt of 5-nitro-o-toluenesulfonic acid and a member of the group consisting of the dilithium, monolithium monosodium and disodium salts of 4,4''-dinitro-2,2''-stilbenedisulfonic acid, in an aqueous reaction medium, in the presence of at least about 0.2 mole, per mole of salts in the mixture, of a base selected from lithium hydroxide and sodium hydroxide, at a temperature of from about 20*C. to the boiling temperature of the reaction medium, in the presence of sufficient ionic lithium to provide a ratio of lithium to sodium in the dye of at least 1:2, and thereafter reacting the condensation product with a reducing agent selected.
Claim 10
Dependent Claim 106 words
In a process for preparing stilbene azo dye by means of an alkaline condensation of a salt of 5-nitro-o-toluenesulfonic acid or of 4,4''-dinitro-2,2''Stilbenedisulfonic acid, the improvement which comprises condensing a member of the group consisting of the lithium salt of 5-nitro-o-toluenesulfonic acid and the dilithium, monolithium monosodium, and disodium salts of 4,4''-dinitro-2,2''-stilbenedisulfonic acid, in an aqueous alkaline reaction medium, at a temperature of from about 20*C. to the boiling temperature of the reaction medium, in the presence of sufficient ionic lithium to provide a ratio of lithium tO sodium in the dye of at least 1:2, until formation of said stilbene azo dye is substantially complete.
Claim 11
Dependent Claim 106 words
In a process for preparing stilbene azo dye by means of an alkaline condensation of a salt of 5-nitro-o-toluenesulfonic acid or of 4,4''-dinitro-2,2''Stilbenedisulfonic acid, the improvement which comprises condensing a member of the group consisting of the lithium salt of 5-nitro-o-toluenesulfonic acid and the dilithium, monolithium monosodium, and disodium salts of 4,4''-dinitro-2,2''-stilbenedisulfonic acid, in an aqueous alkaline reaction medium, at a temperature of from about 20*C. to the boiling temperature of the reaction medium, in the presence of sufficient ionic lithium to provide a ratio of lithium tO sodium in the dye of at least 1:2, until formation of said stilbene azo dye is substantially complete.
Claim 12
Dependent Claim 18 words
The process of claim 8 wherein the product of the condensation reaction is reacted with a reducing agent.
Claim 13
Dependent Claim 32 words
The process of claim 8 wherein the alkaline medium is produced by means of 0.2 mole, per mole of salt being condensed, of a base selected from lithium hydroxide and sodium hydroxide.
Claim 14
Dependent Claim 45 words
The process for the preparation of a solubilized stilbene dye which comprises heating 2-methyl-5-nitrobenzenesulfonic acid in aqueous medium at a temperature of about 40* to about 100*C. and in the presence of at least a stoichiometric amount of lithium hydroxide; said 2-methyl-5-nitrobenzene-sulfonic acid being pure.
Claim 15
Dependent Claim 45 words
The process for the preparation of a solubilized stilbene dye which comprises heating 2-methyl-5-nitrobenzenesulfonic acid in aqueous medium at a temperature of about 40* to about 100*C. and in the presence of at least a stoichiometric amount of lithium hydroxide; said 2-methyl-5-nitrobenzene-sulfonic acid being pure.
Claim 16
Dependent Claim 14 words
A process according to claim 11 in which the lithium hydroxide is added incrementally.

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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1978-09-15 1979-03-17 1979-09-16 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1982-09-15 1983-03-17 1983-09-16 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1986-09-15 1987-03-17 1987-09-16 $7700.00 Window Closed / Lapsed

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