Selective dehydrohalogenation of tertiary halogenated hydrocarbons and removal of tertiary halogenated hydrocarbon impurities from a halogenated hydrocarbon product

Patent metadata

Field	Value
Publication number	US-9745233-B2
Application number	US-201514811244-A
Country	US
Kind code	B2
Filing date	Jul 28, 2015
Priority date	Jun 26, 2009
Publication date	Aug 29, 2017
Grant date	Aug 29, 2017

Abstract

A process for converting tertiary halogenated hydrocarbons in a tertiary halogenated hydrocarbon-containing stream to a corresponding unhalogenated or less-halogenated unsaturated hydrocarbon product with the release of hydrogen halide involves contacting the tertiary halogenated hydrocarbon with a sorbent-type dehydrohalogenation catalyst in a reaction zone and optionally passing a stripping gas through the reaction zone to remove vapor phase reaction products from the reaction zone. A process for removing a tertiary chlorinated hydrocarbon impurity from 1,3-dichloro-1-propene involves contacting a mixture containing the 1,3-dichloro-1-propene and the tertiary chlorinated hydrocarbon impurity with a dehydrochlorination catalyst effective to catalyze a conversion of the tertiary chlorinated hydrocarbon impurity to a corresponding unchlorinated or less-chlorinated unsaturated hydrocarbon and hydrogen chloride and distilling the 1,3-dichloro-1-propene to produce a purified cis-1,3-dichloro-1-propene fraction and a purified trans-1,3-dichloro-1-propene fraction.

First claim

What is claimed is:

1. A method for removing a tertiary halogenated hydrocarbon impurity from a target hydrocarbon compound, comprising:
providing a first mixture comprising a target hydrocarbon compound and a tertiary halogenated hydrocarbon impurity;
contacting the first mixture containing the tertiary halogenated hydrocarbon impurity with a dehydrohalogenation catalyst effective to catalyze a conversion of the tertiary halogenated hydrocarbon impurity to a corresponding unhalogenated or less-halogenated unsaturated hydrocarbon and hydrogen halide, thereby providing a modified mixture; and
distilling the modified mixture to separate and recover a purified target hydrocarbon compound.

2. The method in accordance with claim 1 , wherein the tertiary halogenated hydrocarbon has a boiling point within 5° C. of the boiling point of the target hydrocarbon compound.

3. The method in accordance with claim 1 , wherein the target hydrocarbon compound comprises a halogenated hydrocarbon compound.

4. The method in accordance with claim 1 , wherein said contacting comprises feeding the first mixture containing the tertiary halogenated hydrocarbon impurity into a reactor defining a reaction zone containing the catalyst.

5. The method in accordance with claim 1 , wherein said contacting comprises passing a stripping gas stream through a reaction zone containing the catalyst.

6. The method in accordance with claim 1 :
wherein said feeding comprises feeding a flow stream comprising a liquid mixture including the tertiary halogenated hydrocarbon impurity through the reaction zone at a rate of from 0 to about 4000 weight hourly space velocity (WHSV) or feeding a flow stream comprising a gaseous mixture including the tertiary halogenated hydrocarbon impurity through the reaction zone at a rate of from 0 to about 4000 hr-1 gas hourly space velocity (GHSV);
wherein said contacting comprises contacting the mixture containing the tertiary halogenated hydrocarbon impurity with the dehydrohalogenation catalyst at a temperature of from about 20 to about 200° C. and at a pressure of from about 0.5 to about 50 psia; and
wherein said passing comprises passing the stripping gas stream through the reaction zone at a rate of from 0 to about 4000 hr-1 gas hourly space velocity (GHSV).

7. The method in accordance with claim 1 , wherein the dehydrohalogenation catalyst comprises a sorbent-type dehydrohalogenation catalyst selected from the group consisting of activated alumina, sintered alumina, activated clay, fumed silica, silica gel, magnesium silicate, TiO 2 , Al 2 O 3 , ZrO 2 , AlPO 4 and Al x Si y O z .

8. The method in accordance with claim 7 , wherein the dehydrohalogenation catalyst is doped with a metal.

9. The method in accordance with claim 1 , wherein the conversion is conducted at a temperature of from about 20 to about 150° C.

10. The method in accordance with claim 1 , wherein the conversion is conducted at a pressure of from about 0.5 to about 50 psia.

Assignees

• Dow Agrosciences Llc

Inventors

• Trippeer Michael Lee
• Frank Timothy C
• Au-Yeung Patrick H
• Bronkema Jason L
• Johnston Robin K
• Patel Mukund R
• Holden Bruce S
• Mccabe Terrence
• Hickman Daniel A

Classifications

• C07B2200/09

  Geometrical isomers · CPC title

• C07C17/383

  by distillation · CPC title

• B01D3/009

  in combination with chemical reactions · CPC title

• C07C17/395 Primary

  by treatment giving rise to a chemical modification of at least one compound · CPC title

• B01D3/34

  with one or more auxiliary substances · CPC title