IP Library Granted Patent US 9,617,201
Granted Patent B2
US 9,617,201 · App. 14/509,123 · Granted Apr 11, 2017

Fixed bed process for clay catalyzed alkylation of aromatic amines

Inventors: Mitchel Cohn (West Haven, CT); Ronald Abbott (New Hartford, CT); Alan B. True (New Haven, CT); Huiyuan Chen (Cheshire, CT)
Assignee: CHEMTURA CORPORATION
C07C209/68C07C211/55C07C211/58Y02P20/582
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,617,201
App. No.
14/509,123
Granted
Apr 11, 2017
Kind
B2
Abstract

Aromatic amines, for example, diarylamines such as diphenylamine, dinaphthylamine, N-phenyl-N-naphthyl amine etc., are alkylated by passing a mixture of the amine and an olefin, though a clay catalyst in a fixed bed reactor system. The process is conveniently run as a continued process, produces an alkylated aromatic amine in excellent purity and provides efficiencies in material and energy use.

Claims (17)

1. A process for alkylating an aromatic amine comprising:

a) loading a tubular fixed bed reactor with an acidic bentonite clay,

b) heating or cooling the reactor at a temperature in a range of from about 140° C. to about 180° C.,

c) pumping through the acidic bentonite clay in the fixed bed reactor a liquid mixture of diphenylamine and a mixture of propylene oligomers comprising tri-propylene and/or tetra-propylene to yield a mixture of alkylated aromatic amines comprising

less than 1% by weight, based on all aromatic amines present, of diphenylamine,

about 15% to about 30%, of mono-alkyldiphenyl amine;

60% to about 80%, di-alkyldiphenyl amine; and

0.5 to about 10% of tri-alkyldiphenyl amine.

2. The process according to claim 1 wherein the mixture of propylene oligomers comprises tri-propylene and the product mixture of alkylated aromatic amines is liquid at room temperature.

3. The process according to claim 1 wherein the mixture of propylene oligomers and the diphenylamine are mixed together before being introduced to the fixed bed reactor through the same feed.

4. The process according to claim 1 wherein the mixture of propylene oligomers and the diphenylamine are introduced to the fixed bed reactor separately through different feeds.

5. The process according to claim 3 wherein the mixture of propylene oligomers and the diphenylamine are mixed together in a vessel and heated at temperatures of from about 40° C. up to the first selected reaction temperature before being introduced to the fixed bed reactor.

6. The process according to claim 1 wherein the mole ratio of propylene oligomers to diphenylamine of from about 2:1 to about 4:1.

7. The process according to claim 1 , wherein the mixture comprising diphenylamine and a mixture of propylene oligomers is pumped through the acidic bentonite clay in the fixed bed reactor, the product mixture is collected at elevated temperature while excess propylene oligomers are continuously stripped out.

8. The process according to claim 7 wherein the excess propylene oligomers are continuously stripped out and fed back into the reactor.

9. The process according to claim 7 wherein the fixed bed reactor is a tube of a shell and tube heat exchanger filled with the acidic bentonite clay where the shell is used to maintain temperature control of the reaction mixture.

10. The process according to claim 9 , wherein the reaction product is fed through heat exchanges as heat exchanger fluid.

Assignments (1)
MERGER AND CHANGE OF NAME Recorded Sep 18, 2018
From: CHEMTURA CORPORATION; LANXESS SOLUTIONS US INC.
To: LANXESS SOLUTIONS US INC.
Reel/Frame 046901/0439 →
Continuity (2)
Provisional Application 61890392 · Oct 14, 2013
Related Publication 20150105588A1 · Apr 16, 2015