Frederick A. Hohorst
Kansas State University
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Featured researches published by Frederick A. Hohorst.
Environmental Science & Technology | 1982
Lawrence Stein; Frederick A. Hohorst
Although it is generally considered to be inert, radon reacts spontaneously at ambient temperature with a number of fluorine-containing compounds, including dioxygenyl salts, fluoronitrogen salts, and halogen fluoride-metal fluoride complexes. A method for the collection of radon from air, using either dioxygenyl hexafluoroantimonate (O/sub 2//sup +/SbF/sub 6//sup -/) or hexafluoroiodine hexafluoroantimonate (IF/sub 6//sup +/SbF/sub 6//sup -/) reagent, is described. The air is passed though a drying tube and then through a bed of the reagent, which captures radon as a nonvolatile product. In tests with radon-air mixtures containing 45-210000 pCi/L of radon-222, more than 99% of the radon was retained by beds of powders (2.3-3.0 g of compound/cm/sup 2/) and pellets (7.5-10.9 g of compound/cm/sup 2/). The gas mixtures were designed to simulate radon-contaminated atmospheres in underground uranium mines. No dependence of collection efficiency upon radon concentration was observed. The method can be used for the analysis of radon-222 (by measurement of the ..gamma.. emissions of the short-lived daughters, lead-214 and bismuth-214) and the purification of small volumes of air.
Journal of Inorganic and Nuclear Chemistry | 1976
Frederick A. Hohorst; Darryl D. DesMarteau
FLUOROCARBON peroxides can now be obtained in considerable variety by the direct addition of the CF3OOgroup to suitable substrates. We have previously demonstrated the utility of trifluoromethyl hydroperoxide, CF3OOH[1--4], and bis(trifluoromethyl) trioxide, CF3OsCF315-7], in the direct synthesis of novel organic and inorganic peroxides. The reaction of CF303CF3 with alkenes gives rise to an interesting series of compounds of the type, CFsOOCR~R:CR2R4OCF3 and the method is quite general. In order to extend this kind of reaction to related derivatives containing only the peroxide linkage, we have investigated the reactions of fluoroperoxytrifluoromethane, CFsOOF and chloroperoxytrifluoromethane, CF3OOCI[8] with certain alkenes. These reagents can yield peroxides which differ only in the substitution of a fluorine by chlorine and along with the derivatives obtained with CF303CF3, allows one in principle to obtain a related series of peroxides of the general formulas CF3OOCRtR2CR3R4OCF3, CF3OOCRIR2CR3R4F and CF3OOCRMR2CR3R4CI. The addition of CF3OOF and CF3OOC1 to certain alkenes occurs readily at low temperatures according to the general equations
Journal of The Chemical Society, Chemical Communications | 1973
Frederick A. Hohorst; Darryl D. DesMarteau
The addition of bistrifluoromethyl trioxide to chlorotrifluoroethylene at 70° produces the peroxides CF3·O·O·CF2·CFCl·O·CF3 and CF3·O·CF2·CFCl·O·O·CF3.
Journal of the American Chemical Society | 1973
Frederick A. Hohorst; Darryl D. DesMarteau; L. R. Anderson; D. E. Gould; W. B. Fox
Inorganic Chemistry | 1974
Frederick A. Hohorst; Darryl D. DesMarteau
Journal of the American Chemical Society | 1971
Darryl D. DesMarteau; Peter A. Bernstein; Frederick A. Hohorst
Inorganic Chemistry | 1971
Darryl D. DesMarteau; Peter A. Bernstein; Frederick A. Hohorst; Max Eisenberg
Inorganic Chemistry | 1975
Frederick A. Hohorst; Lawrence Stein; Elizabeth. Gebert
Journal of Organic Chemistry | 1974
Frederick A. Hohorst; Joseph V. Paukstelis; Darryl D. DesMarteau
ChemInform | 1974
Frederick A. Hohorst; Darryl D. DesMarteau