Weir quench and processes incorporating the same
US-2015217256-A1 · Aug 6, 2015 · US
US9598334B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9598334-B2 |
| Application number | US-201314429263-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 13, 2013 |
| Priority date | Sep 20, 2012 |
| Publication date | Mar 21, 2017 |
| Grant date | Mar 21, 2017 |
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Processes for the production of chlorinated propenes are provided. The present processes make use of 1,2-dichloropropane, a by-product in the production of chlorohydrin, as a low cost starting material, alone or in combination with 1,2,3-trichloropropane. At least one dehydrochlorination is conducted in the gas phase, and is the first process step. The present processes can also generate anhydrous HCl as a byproduct that can be removed from the process and used as a feedstock for other processes, providing further time and cost savings.
Opening claim text (preview).
The invention claimed is: 1. A process for the production of chlorinated propenes from one or more chlorinated alkanes comprising 1,2-dichloropropane, comprising at least one gas phase dehydrochlorination step that is the first reaction step, wherein the gas phase dehydrochlorination is carried out without the use of a catalyst and at a pressure greater than ambient, wherein the gas phase dehydrochlorination produces one or more monochloropropenes; and wherein the one or more monochloropropenes are separated from the 1,2-dichloropropane, and after separation, the one or more monochloropropenes are subjected to at least one liquid phase chlorination step. 2. The process of claim 1 , wherein the chlorinated propenes comprise dichloropropenes, trichloropropenes, and/or tetrachloropropenes. 3. The process of claim 1 , wherein the one or more chlorinated alkanes further comprise 1,2,3-trichloropropane. 4. The process of claim 1 , comprising at least one additional dehydrochlorination step. 5. The process of claim 4 , wherein at least one additional dehydrochlorination step is conducted in the liquid phase, in the presence of one or more catalysts. 6. The process of claim 4 , wherein at least one additional dehydrochlorination step is conducted in the liquid phase, in the presence of caustic. 7. The process of claim 1 , wherein at least one chlorination step is conducted in the gas phase. 8. The process of claim 1 , wherein at least one chlorination step is conducted in the liquid phase. 9. The process of claim 1 , wherein HC1 is generated as a byproduct. 10. The process of claim 9 , wherein HC1 is recovered as anhydrous HC1. 11. The process of claim 1 , wherein the dehydrochlorination step is conducted at 200° C. or greater. 12. The process of claim 1 , wherein the 1,2-dichloropropane conversion is from 30% to 70%. 13. The process of claim 12 , wherein the 1,2-dichloropropane conversion is from 40% to 60%.
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