IP Library Granted Patent US 8,362,192
Granted Patent B2
US 8,362,192 · App. 12/937,849 · Granted Jan 29, 2013

Large scale process for polymerization of DAPBI-containing polyaramid

Inventors: Richard Elena Theodorus Petrus De Vos (Arnhem, NL); Joannes Marinus Surquin (Arnhem, NL); Marlieke Elisabeth Josephine Pepels (Nijmegen, NL)
Assignee: Teijin Aramid B.V.
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Quick Facts
Patent No.
US 8,362,192
App. No.
12/937,849
Granted
Jan 29, 2013
Kind
B2
Abstract

A method for obtaining an aromatic polyamide crumb from an aromatic diamine and an aromatic diacid chloride, which aromatic polyamide comprises 5(6)-amino-2-(p-aminophenyl)benzimidazole terephthalamide units and has a relative viscosity η rel of at least 3, by: (1) adding at least monomers (i)-(iii) in N-methyl pyrrolidone as solvent wherein (i) is 0-30 mole % para-phenylenediamine (PPD), (ii) is 20-50 mole % 5(6)-amino-2-(p-aminophenyl)benzimidazole (DABPI), (iii) is 49.05-50.05 mole % terephthaloyl dichloride (TDC), and optionally calcium chloride to obtain a CaCl 2 /aromatic diamine molar ratio less than 0.5, and an aromatic diamine/aromatic diacid chloride ratio between 0.99 and 1.01; (2) mixing the monomers and the optional calcium chloride to a homogenous mixture having a monomer concentration of 5 to 12 wt %; followed by (3) adding calcium chloride to the homogeneous mixture to obtain a CaC1 2 /aromatic diamine molar ratio 0.6-1.0; and (4) polymerizing the mixture.

Claims (14)

1. A method for obtaining an aromatic polyamide crumb from an aromatic diamine and an aromatic diacid chloride, which aromatic polyamide comprises 5(6)-amino-2-(p-aminophenyl)benzimidazole terephthalamide units and has a relative viscosity η rel of at least 3, comprising:

adding at least monomers (i)-(iii) in N-methyl pyrrolidone as solvent wherein:

i) is 0-30 mole % para-phenylenediamine (PPD);

ii) is 20-50 mole % 5(6)-amino-2-(p-aminophenyl)benzimidazole (DABPI);

iii) is 49.05-50.05 mole % terephthaloyl dichloride (TDC); and optionally calcium chloride to obtain a CaCl 2 /aromatic diamine molar ratio less than 0.5, and an aromatic diamine/aromatic diacid chloride ratio between 0.99 and 1.01;

mixing the monomers and the optional calcium chloride to a homogeneous mixture having a monomer concentration of 5 to 12 wt %, followed by

adding calcium chloride to the homogeneous mixture to obtain a CaCl 2 /aromatic diamine molar ratio of 0.6-1.0; and

polymerizing the mixture in a reactor having a measure capacity of at least 160 L, wherein mole % relates to the molar percentage of the monomers with regard to the total of aromatic diamine and aromatic diacid chloride monomers.

2. The method according to claim 1 wherein the CaCl 2 /aromatic diamine molar ratio in the homogeneous mixture is 0.65-0.85.

3. The method according to claim 2 wherein the CaCl 2 /aromatic diamine molar ratio in the homogeneous mixture is 0.70-0.80.

4. The method according to claim 1 wherein first the aromatic diamines are mixed for 1 to 180 min in N-methyl pyrrolidone wherein the CaCl 2 /aromatic diamine molar ratio is 0, after which the aromatic diacid chlorides are added and mixed for another 1 to 180 min followed by adding calcium chloride to obtain a CaCl 2 /aromatic diamine molar ratio 0.6-1.0.

5. The method according to claim 1 wherein calcium chloride is added as an NMP/CaCl 2 mixture.

6. The method according to claim 1 which is performed in a cylindrical reactor having a measure capacity of at least 160 L, which is equipped with a single mixing gear for use as stirrer and granulator.

7. The method according to claim 1 , wherein first the aromatic diamines are mixed for 3-30 min in N-methyl pyrrolidone wherein the CaC 1 2 /aromatic diamine molar ratio is 0, after which the aromatic diacid chlorides are added and mixed for another 3-30 min, followed by adding calcium chloride to obtain a CaCl 2 /aromatic diamine molar ratio of 0.6-1.0.

Assignments (3)
CHANGE OF ADDRESS Recorded Apr 6, 2012
From: TEIJIN ARAMID B.V.
To: TEIJIN ARAMID B.V.
Reel/Frame 028169/0439 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2012
From: DE VOS, RICHARD ELENA THEODOROUS PETRUS; SURQUIN, JOANNES MARINUS; PEPELS, MARLIEKE ELIZABETH JOSEPHINE
To: TEIJIN TWARON B.V.
Reel/Frame 028006/0869 →
CHANGE OF NAME Recorded Apr 6, 2012
From: TEIJIN TWARON B. V.
To: TEIJIN ARAMID B. V.
Reel/Frame 028007/0970 →
Priority Claims (1)
EP 08007566 · Apr 18, 2008 · regional
Continuity (1)
Related Publication 20110046340A1 · Feb 24, 2011