Unlock instant, AI-driven research and patent intelligence for your innovation.

Processes for producing trifluoroiodomethane and trifluoroacetyl iodide

A technology of trifluoroiodomethane and trifluoroacetyl, which is applied in the gas phase field of producing trifluoroiodomethane and trifluoroacetyl iodide, and can solve problems such as process efficiency reduction

Pending Publication Date: 2021-04-30
HONEYWELL INT INC
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Additional steps required for separation and handling make the process less efficient

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Processes for producing trifluoroiodomethane and trifluoroacetyl iodide
  • Processes for producing trifluoroiodomethane and trifluoroacetyl iodide
  • Processes for producing trifluoroiodomethane and trifluoroacetyl iodide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0104] Example 1: Manufacture of trifluoroacetyl iodide at higher reaction temperatures according to Equation 1

[0105]In this example, the production of trifluoroacetyl iodide from hydrogen iodide and trifluoroacetyl chloride at higher temperatures according to Equation 1 as described above is demonstrated. In a series of twenty-three experiments, equimolar amounts of trifluoroacetyl chloride and anhydrous hydrogen iodide were passed through a preheater and heated to a temperature of about 100°C. The heated reactants were passed through a stainless steel tube having a diameter of 3 / 8 inch (9.5 mm) and a length of 6 inches (152 mm). Depending on the experiment, the tubes were heated to a temperature ranging from 200°C to 350°C, and were purged with nitrogen for at least one hour before each experiment to remove any water. In twenty-one experiments, the tubes contained one of several catalysts. In the remaining two experiments, the tubes contained no catalyst. Contact tim...

Embodiment 2

[0114] Example 2: Production of trifluoroacetyl iodide at higher reaction temperatures according to Equation 1

[0115] In this example, the production of trifluoroacetyl iodide from hydrogen iodide and trifluoroacetyl chloride at higher reaction temperatures according to Equation 1 as described above is demonstrated. A flow rate of 8.34 grams / hour of trifluoroacetyl chloride and a flow rate of 14.08 grams / hour of hydrogen iodide were passed through a stainless steel tube 3 / 8 inch (9.5 mm) in diameter and 6 inches (152 mm) in length. The tubes were heated to about 300°C and purged with nitrogen for at least one hour prior to the experiment to remove any water. tube contains Stainless steel catalyst, contact time is about 10 seconds. The process ran continuously for 6.25 hours. The output of the reactor was collected in two dry ice traps, one at about 0°C to -5°C and the other at about -78°C.

[0116] A total of 99.8 g of material was collected and a portion was analyzed...

Embodiment 3

[0117] Example 3: Production of trifluoroacetyl iodide at higher reaction temperatures according to Equation 1

[0118] In this example, the production of trifluoroacetyl iodide from hydrogen iodide and trifluoroacetyl chloride at higher reaction temperatures according to Equation 1 as described above is demonstrated. A flow rate of 5.75 grams / hour of trifluoroacetyl chloride and a flow rate of 13.9 grams / hour of hydrogen iodide were passed through a stainless steel tube having a diameter of 1 / 2 inch (12.7 mm) and a length of 6 inches (152 mm). The tubes were heated to about 250°C and purged with nitrogen for at least one hour prior to the experiment to remove any water. The tube contained 0.5% palladium on alumina support (3.2 mm pellets) catalyst with a contact time of about 15 seconds. The process ran continuously for 5.25 hours. The output of the reactor was collected in two dry ice traps, one at about 0°C to -5°C and the other at about -78°C.

[0119] A total of 89 g...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
diameteraaaaaaaaaa
areaaaaaaaaaaa
Login to View More

Abstract

The present disclosure provides a process for producing trifluoroiodomethane, the process comprising providing a reactant stream comprising hydrogen iodide and at least one trifluoroacetyl halide selected from the group consisting of trifluoroacetyl chloride, trifluoroacetyl fluoride, trifluoroacetyl bromide, and combinations thereof, reacting the reactant stream in the presence of a first catalyst at a first reaction temperature from about 25 DEG C to about 400 DEG C to produce an intermediate product stream comprising trifluoroacetyl iodide, and reacting the intermediate product stream in the presence of a second catalyst at a second reaction temperature from about 200 DEG C to about 600 DEG C to produce a final product stream comprising the trifluoroiodomethane.

Description

technical field [0001] The present disclosure relates to the production of trifluoroiodomethane (CF 3 I) and trifluoroacetyl iodide (CF 3 COI) method. In particular, the present disclosure relates to gas phase processes for the production of trifluoroiodomethane and trifluoroacetyl iodide. Background technique [0002] Trifluoroacetyl iodide (CF 3 COI) is convertible into trifluoroiodomethane (CF 3 I) compounds. Trifluoroiodomethane (CF 3 I) Also known as perfluoromethyl iodide, trifluoromethyl iodide or iodotrifluoromethane, are compounds that are used in commercial applications as, for example, refrigerants or fire extinguishing agents. Trifluoroiodomethane is a low global warming potential molecule with negligible ozone depletion potential. Trifluoroiodomethane can replace substances that are more harmful to the environment. [0003] Methods for the preparation of trifluoroacetyl iodide are known. For example, the article "Reactions of metal salts of acids with h...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C07C17/093C07C17/20C07C17/10C07C17/42C07C19/16B01J21/18
CPCC07C51/60C07C51/64B01J21/18B01J23/745B01J23/755B01J23/866B01J23/862B01J23/883B01J23/8878B01J23/72B01J21/04B01J23/42B01J23/44B01J27/22C07C17/361B01J35/19C07C53/48C07C19/08C07C17/093C07C17/206C07C17/10C07C17/42C07C19/16C07C17/20C07C17/35B01J27/224
Inventor 哈里达桑·K·奈尔格伦·马蒂斯拉吉夫·拉特纳·辛格特里斯·杨王海友赖安·J·赫尔斯拉吉夫·巴纳瓦利
Owner HONEYWELL INT INC