Binary catalyst based selective catalytic reduction filter
US-9764287-B2 · Sep 19, 2017 · US
US2021317062A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2021317062-A1 |
| Application number | US-202117219390-A |
| Country | US |
| Kind code | A1 |
| Filing date | Mar 31, 2021 |
| Priority date | Apr 8, 2020 |
| Publication date | Oct 14, 2021 |
| Grant date | — |
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The present disclosure provides a process for making trifluoroacetyl iodide (TFAI) in a liquid phase reaction. Specifically, the present disclosure provides a liquid phase reaction of trifluoroacetyl chloride (TFAC) and hydrogen iodide (HI), with or without a catalyst, to form trifluoroacetyl iodide (TFAI). The reaction may be performed at ambient or elevated temperatures.
Opening claim text (preview).
1 . A process for producing trifluoroacetyl iodide (TFAI) in a liquid phase reaction, the process comprising: providing trifluoroacetyl chloride, hydrogen iodide, and an optional catalyst; reacting the trifluoroacetyl chloride and hydrogen iodide to provide trifluoroacetyl iodide. 2 . The process of claim 1 , wherein in the providing step, the mole ratio of the trifluoroacetyl chloride to the hydrogen iodide is from about 1:10 to about 10:1. 3 . The process of claim 1 , wherein in the providing step, a weight ratio of the catalyst to the trifluoroacetyl chloride may be from about 0.001:1 to about 0.5:1. 4 . The process of claim 1 , wherein the catalyst is selected from the group consisting of silicon carbide, activated carbon, carbon molecular sieves, and combinations thereof. 5 . The process of claim 1 , wherein in the reacting step, the trifluoroacetyl chloride, the hydrogen iodide, and the optional catalyst are at a temperature from 0° C. to 200° C. 6 . A process for producing trifluoroacetyl iodide (TFAI) in a liquid phase reaction, the process comprising: mixing trifluoroacetyl chloride, hydrogen iodide, and an optional catalyst; and heating the trifluoroacetyl chloride, hydrogen iodide, and an optional catalyst to produce trifluoroacetyl iodide and hydrogen chloride. 7 . The process of claim 6 , further including separating the trifluoroacetyl iodide from the hydrogen chloride, trifluoroacetyl chloride, and hydrogen iodide. 8 . The process of claim 6 , wherein the process is a continuous process. 9 . The process of claim 6 , wherein the process is a batch process. 10 . The process of claim 6 , wherein the catalyst is selected from the group consisting of silicon carbide, activated carbon, carbon molecular sieves, and combinations thereof. 11 . The process of claim 6 , wherein in the reacting step, the trifluoroacetyl chloride, the hydrogen iodide, and the optional catalyst are at a temperature from 0° C. to 200° C. 12 . The process of claim 6 , wherein in the reacting step, the trifluoroacetyl chloride, the hydrogen iodide, and the optional catalyst are at a pressure of 5 psig to 500 psig.
Silicon carbide · CPC title
Continuous processes · CPC title
Batch processes · CPC title
Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof · CPC title
Carbon · CPC title
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