GB859492A - Preparation of perchloryl fluoride - Google Patents
Preparation of perchloryl fluorideInfo
- Publication number
- GB859492A GB859492A GB35698/58A GB3569858A GB859492A GB 859492 A GB859492 A GB 859492A GB 35698/58 A GB35698/58 A GB 35698/58A GB 3569858 A GB3569858 A GB 3569858A GB 859492 A GB859492 A GB 859492A
- Authority
- GB
- United Kingdom
- Prior art keywords
- perchlorate
- fluorinating agent
- mixture
- reaction temperature
- reaction time
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B7/00—Halogens; Halogen acids
- C01B7/24—Inter-halogen compounds
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B11/00—Oxides or oxyacids of halogens; Salts thereof
- C01B11/24—Oxygen compounds of fluorine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
<PICT:0859492/III/1> perchloryl fluoride gas is produced by interaction of an inorganic perchlorate and a fluorinating agent consisting of a mixture of fluosulphonic acid and antimony pentafluoride. The influence on the yield of increasing the proportion of antimony pentafluoride is shown by the Figure. The perchlorate may be added to the mixture or to either of the constituents before mixing. Ammonium, lithium, sodium, potassium, silver, magnesium, calcium, barium, and nitrosyl perchlorate are specified. Sufficient fluorinating agent to dissolve the perchlorate completely is preferably employed, i.e. not less than about 5 parts of fluorinating agent per part of perchlorate. The reaction temperature may be 70-130 DEG C. and the reaction time 2-24 hours. In continuous operation the reaction temperature is preferably 100-135 DEG C. and the reaction time 1-10 minutes. Examples are given.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US859492XA | 1957-11-07 | 1957-11-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB859492A true GB859492A (en) | 1961-01-25 |
Family
ID=22195035
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB35698/58A Expired GB859492A (en) | 1957-11-07 | 1958-11-06 | Preparation of perchloryl fluoride |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB859492A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2253588A1 (en) * | 2008-03-10 | 2010-11-24 | Central Glass Company, Limited | Method for producing oxygen-containing halogenated fluoride |
-
1958
- 1958-11-06 GB GB35698/58A patent/GB859492A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2253588A1 (en) * | 2008-03-10 | 2010-11-24 | Central Glass Company, Limited | Method for producing oxygen-containing halogenated fluoride |
EP2253588A4 (en) * | 2008-03-10 | 2012-08-01 | Central Glass Co Ltd | Method for producing oxygen-containing halogenated fluoride |
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