IP Library Granted Patent US 9,289,758
Granted Patent B2
US 9,289,758 · App. 14/521,449 · Granted Mar 22, 2016

Processes for producing chlorinated hydrocarbons and methods for recovering polyvalent antimony catalysts therefrom

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Quick Facts
Patent No.
US 9,289,758
App. No.
14/521,449
Granted
Mar 22, 2016
Kind
B2
Abstract

The preparation of chlorinated hydrocarbons, such as pentachloropropanes, such as 1,1,1,2,3-pentachloropropane, from tetrachloropropanes, such as 1,1,1,3-tetrachloropropane, in the presence of a polyvalent antimony compound that includes a pentavalent antimony compound, such as antimony pentachloride, is described. Also described are methods for preparing optionally chlorinated alkenes, such as, tetrachloropropenes, from chlorinated alkanes, such as pentachloropropanes, in the presence of polyvalent antimony compound that includes a pentavalent antimony compound, as well as methods for recovering polyvalent antimony compounds from such processes.

Claims (17)

1. A method of forming an alkene product comprising,

heating a chlorinated alkane substrate in the presence of at least one polyvalent antimony compound comprising at least one pentavalent antimony compound, thereby forming a product comprising said alkene product, wherein

said alkene product optionally has at least one chlorine group covalently bonded thereto, and

said chlorinated alkane substrate and said alkene product each have a carbon backbone structure that is in each case the same.

2. The method of claim 1 , wherein the heating of the chlorinated alkane substrate in the presence of the at least one polyvalent antimony compound is substantially free of iron chloride, iron metal, and/or trialkylphosphate.

3. The method of claim 1 , wherein the heating of the chlorinated alkane substrate in the presence of the at least one polyvalent antimony compound is conducted in the presence of less than about 5 weight percent of iron chloride, iron metal, and/or trialkylphosphate, on a basis of weight of chlorinated alkane substrate.

4. The method of claim 1 , wherein the heating of the chlorinated alkane substrate in the presence of the at least one polyvalent antimony compound is conducted in the presence of less than about 1 weight percent of iron chloride, iron metal, and/or trialkylphosphate, on a basis of weight of chlorinated alkane substrate.

5. The method of claim 1 , wherein the heating of the chlorinated alkane substrate in the presence of the at least one polyvalent antimony compound is conducted in the presence of less than about 0.1 weight percent of iron chloride, iron metal, and/or trialkylphosphate, on a basis of weight of chlorinated alkane substrate.

6. The method of claim 1 , wherein the heating of the chlorinated alkane substrate in the presence of the at least one polyvalent antimony compound comprising a pentavalent antimony compound to thereby form a product comprising said alkene product is conducted in the absence of iron chloride, iron metal, and/or trialkylphosphate.

7. The method of claim 1 , wherein the heating of the chlorinated alkane substrate is conducted in the presence of the at least one polyvalent antimony compound as the sole catalyst present in the reaction.

8. The method of claim 2 , wherein the iron chloride comprises ferric chloride and/or ferrous chloride.

9. The method of claim 1 , wherein the pentavalent antimony compound comprises one or more pentavalent antimony compounds represented by the following Formula (I),

Sb(R 1 ) a (Cl) b   (I)

wherein the sum of a and b is 5, provided that b is at least 2, and

R 1 independently for each a is selected from the group consisting of linear, branched, or cyclic alkyl, and aryl.

10. The method of claim 9 , wherein the pentavalent antimony compound comprises antimony pentachloride.

11. The method of claim 1 , wherein the heating of 1,1,1,3,3-pentachloropropane is carried out in the presence of at least one polyvalent antimony compound comprising at least one pentavalent antimony compound and 1,1,1,2,3-pentachloropropane.

Assignments (8)
MERGER Recorded Aug 9, 2017
From: AXIALL OHIO, INC.
To: EAGLE US 2 LLC
Reel/Frame 043242/0798 →
RELEASE OF SECURITY INTEREST Recorded Sep 18, 2016
From: BARCLAYS BANK PLC, AS COLLATERAL AGENT
To: AXIALL CORPORATION; ROYAL MOULDINGS LIMITED; PLASTIC TRENDS, INC.; AXIALL OHIO, INC.; GEORGIA GULF CORPORATION; EXTERIOR PORTFOLIO, LLC
Reel/Frame 039857/0569 →
SUBSTITUTION OF ADMINISTRATIVE AGENT & ASSIGNMENT OF RIGHTS UNDER CREDIT AGREEMENT AND LOAN DOCUMENTS Recorded Sep 16, 2016
From: GENERAL ELECTRIC COMPANY, AS ADMINISTRATIVE AGENT
To: WELLS FARGO CAPITAL FINANCE, LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 040055/0068 →
RELEASE OF SECURITY INTEREST Recorded Sep 16, 2016
From: WELLS FARGO CAPITAL FINANCE, LLC
To: AXIALL, LLC; ROME DELAWARE CORP.; AXIALL OHIO, INC.; ROYAL GROUP, INC.; GROUPE ROYAL, INC.
Reel/Frame 040057/0826 →
SUBSTITUTION OF ADMINISTRATIVE AGENT AS SUCCESSOR BY MERGER Recorded Sep 15, 2016
From: GENERAL ELECTRIC CAPITAL CORPORATION, AS ADMINISTRATIVE AGENT
To: GENERAL ELECTRIC COMPANY, ADMINISTRATIVE AGENT AS SUCCESSOR BY MERGER
Reel/Frame 040054/0179 →
SECURITY AGREEMENT Recorded Mar 3, 2015
From: AXIALL CORPORATION; ROYAL MOULDINGS LIMITED; PLASTIC TRENDS, INC.; GEORGIA GULF CORPORATION; EXTERIOR PORTFOLIO, LLC; AXIALL OHIO, INC.
To: BARCLAYS BANK PLC, AS COLLATERAL AGENT
Reel/Frame 035121/0600 →
PATENT SECURITY AGREEMENT Recorded Dec 19, 2014
From: AXIALL OHIO, INC.; ROYAL MOULDINGS LIMITED; PLASTIC TRENDS, INC.; AXIALL CORPORATION; ROYAL GROUP, INC.; GROUPE ROYAL, INC.
To: GENERAL ELECTRIC CAPITAL CORPORATION
Reel/Frame 034687/0463 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2014
From: SHERWOOD, SCOTT A.; LESTER, STEPHEN ROBERT
To: AXIALL OHIO, INC.
Reel/Frame 034118/0324 →