Amine salts of lignosulfonates

• US 4,797,157 A
• Filed: 01/22/1988
• Issued: 01/10/1989
• Est. Priority Date: 10/03/1985
• Status: Expired due to Term

• Current Assignee: Westvaco Corporation (Meadwestvaco Corporation)
• Original Assignee: Westvaco Corporation (Meadwestvaco Corporation)
• Inventors: Davis, James E., DelliColli, Humbert T., Dilling, Peter
• Primary Examiner(s): NOT, DEFINED
• Application Number:
  US07/147,340
• Time in Patent Office: 354 Days
• Field of Search: 106/20, 106/123.1
• US Class Current: 106/31.43
• CPC Class Codes: A01N 25/30 characterised by the surfactants
• CPC Class Codes: C08H 6/00 Macromolecular compounds derived from lignin, e.g. tannins, humic acids
• CPC Class Codes: C09B 67/0086 anionic dispersing agents
• CPC Class Codes: C09D 11/03 characterised by features other than the chemical nature of the binder
• CPC Class Codes: D06P 1/46 using compositions containing natural macromolecular substances or derivatives thereof

Abstract

Disclosed is a method for the production of a sulfomethylated lignin amine salt from the lignin by-product of the black liquor residue of a kraft pulping process and the use of lignin amine salts as additives in other chemical compositions. The lignin amine salt is produced by precipitating lignin from the block liquor and reacting the precipitated lignin slurry with formaldehyde. Thereafter, the lignin slurry is acidified to a pH of about 2 to 3 and water-washed to remove inorganic salts and other impurities therefrom. The washed methylolated lignin is reacted with an organic amine and a sulfur-oxygen-containing compound, such as sulfur dioxide to form the sulfomethylated lignin amine salt.

The sulfomethylated lignin amine salt products are disclosed as an additive in dyestuff and printing ink compositions, as well as a sequestrant in pesticide compositions, with improved results over certain lignin salts heretofore employed as additives in such compositions.

Claims

1. A printing ink composition comprising a printing paste gel and, as an additive therein, a sulfomethylated lignin amine salt prepared according to the steps of:

(a) ionizing the phenol component of a lignin material in alkaline liquid medium;

(b) methylolating the lignin material in the ortho position of the phenol component;

(c) lowering the pH of the liquid to an acid pH to precipitate the methylolated lignin material;

(d) washing the precipitated lignin material with water to remove inorganic salts and residual reactants therefrom; and

(e) reacting the washed, purified methylolated lignin material with an amine compound and a sulfur-oxygen-containing compound in liquid medium to produce sulfomethylated lignin amine salt.

2. The composition as defined in claim 1 wherein the washed, purified methylolated lignin material is reacted with the amine and sulfur-oxygen-containing compound in liquid medium by first adding the amine compound to the lignin in liquid medium at a pH of around 6 to 7, and the sulfur-oxygen-containing compound is thereafter added to the lignin amine composition in sufficient amount to sulfonate the composition and form the lignosulfonated amine salt at a pH of about 6 to 7.

3. The composition as defined in claim 2 wherein the amine is selected from the group consisting of trimethylamine, triethylamine, triethanolamine, diethanolamine, dimethylamine, and monoethanolamine, propylene diamine, cyclohexylamine, diethylene tetramine, tetraethylene, and pentamine.

4. The composition as defined in claim 3 wherein the sulfur-oxygen-containing compound is sulfur dioxide gas.

5. The composition as defined in claim 1 wherein the purified methylolated lignin material is reacted with the amine and sulfur-oxygen-containing compound to form the amine salt by first reacting the amine and sulfur-oxygen-containing compound to form an amine sulfite, and thereafter reacting the amine sulfite with the lignin to form the lignosulfonate amine salt.

6. The composition as defined in claim 1 wherein the sulfur-oxygen-containing compound is added to the amine/methylolated lignin composition at a pH of about 6.3 to 6.5.