IP Library Granted Patent US 10,240,282
Granted Patent B2
US 10,240,282 · App. 14/371,760 · Granted Mar 26, 2019

Process for preparing aramid copolymer yarn using a halide acid wash

Inventors: Steven R. Allen (Midlothian, VA); Vlodek Gabara (Richmond, VA); Joseph Lenning Lowery (Midlothian, VA); Christopher William Newton (Richmond, VA); David J. Rodini (Midlothian, VA); Andrew J. Sitter (Mechanicsville, VA)
Assignee: E I DU PONT DE NEMOURS AND COMPANY
D06M11/26D01D10/06D01F6/805
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Quick Facts
Patent No.
US 10,240,282
App. No.
14/371,760
Granted
Mar 26, 2019
Kind
B2
Abstract

The present invention concerns methods for removing sulfur from yarn comprising the steps of: a) contacting never-dried polymeric yarn with an aqueous base, the polymer comprising imidazole groups and said polymer comprising sulfur atoms characterized as being in the form of sulfate anions; b) contacting the yarn with an aqueous acid comprising a halide; and c) rinsing the yarn.

Claims (19)

1. A process for removing sulfur from yarn comprising the steps of:

a) contacting never-dried polymeric yarn with an aqueous base, said polymeric yarn made from polymer comprising imidazole groups and said polymer comprising sulfur atoms in the form of sulfate anions; and subsequently

b) contacting the yarn with an aqueous acid comprising a halide; and

c) rinsing the yarn.

2. The process of claim 1 , further comprising rinsing the yarn after step a) but prior to step b).

3. The process of claim 2 , wherein the rinsing of the yarn in claim 2 is an aqueous rinse.

4. The process of claim 1 , wherein said polymer comprises residues of 5(6)-amino-2-(p-aminophenyl)benzimidazole, aromatic diamine, and aromatic diacid-chloride.

5. The process of claim 4 , wherein said aromatic diacid-chloride is terephthaloyl dichloride.

6. The process of claim 4 , wherein said aromatic diamine is para-phenylenediamine.

7. The process of claim 4 , wherein the molar ratio of 5(6)-amino-2-(p-aminophenyl)benzimidazole to aromatic diamine is in the range of from 30/70 to 85/15.

8. The process of claim 4 wherein the molar ratio of 5(6)-amino-2-(p-aminophenyl)benzimidazole to aromatic diamine is 45/55 to 85/15.

9. The process of claim 1 , wherein the acid comprising a halide is one or more of hydrofluoric acid, hydrochloric acid, hydrobromic acid, hydroiodic acid, or mixtures thereof.

10. The process of claim 9 , wherein said acid comprising a halide is hydrochloric acid.

11. The process of claim 1 , wherein the halide acid is formed from a material that forms a halide-containing acid when in contact with water.

12. The process of claim 1 , wherein in step (c) the yarn is rinsed with water.

13. The process of claim 1 , wherein at least a portion of residual halide anions is removed from the fiber in step c).

14. The process of claim 1 , wherein after step c), the yarn has 3.0 weight percent sulfur or less, based on the weight of the yarn.

15. The process of claim 14 , wherein after step c), the yarn has 2.5 weight percent sulfur or less, based on the weight of the yarn.

16. The process of claim 15 , wherein after step c), the yarn has 1.0 weight percent sulfur or less, based on the weight of the yarn.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2019
From: E. I. DU PONT DE NEMOURS AND COMPANY
To: DUPONT SAFETY & CONSTRUCTION, INC.
Reel/Frame 049585/0450 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2014
From: ALLEN, STEVEN R.; GABARA, VLODEK; LOWERY, JOSEPH LENNING; NEWTON, CHRISTOPHER WILLIAM; RODINI, DAVID J.; SITTER, ANDREW J.
To: E. I. DUPONT DE NEMOURS AND COMPANY
Reel/Frame 033363/0189 →
Continuity (1)
Related Publication 20140331415A1 · Nov 13, 2014