• Bulletin of the Korean Chemical Society
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• v.22 no.5
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• pp.441-442
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• 2001

• Applied Chemistry for Engineering
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• v.9 no.4
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• pp.523-528
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• 1998

The electrochemical characteristics of $V_2O_5$ as working electrode were studied in the cell (1-butene+$O_2$, $V_2O_5{\mid}YSZ{\mid}Ag$, $O_2$) with a YSZ solid electrolyte. The sintering of Ag as a counter electrode was occurred after calcination, and the structure which has the pores of over $3{\mu}m$ was achieved. In particular, the peak of (010) plane of the working electrode on the XRD spectrum which is responsible for selective oxidation appeared after calcination. The major product of 1-butene oxidation over $V_2O_5$ was butadiene. The technique of SEP (solid electrolyte potentiometry) was used to monitor the chemical potential of chemical species adsorbed on the working electrode. Over a wide range of gas compositions of 1-butene and oxygen, open circuit voltage (OCV) exhibited the mixed potential of surface oxygen activity.

• Bulletin of the Korean Chemical Society
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• v.34 no.6
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• pp.1751-1754
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• 2013

3,4-Dihydropyrimidin-2(1H)-ones were efficiently converted into the corresponding pyrimidin-2(1H)-ones in high yields within a short period of time on treatment with aqueous acetonitrile using 1,4-bis(triphenylphosphonium)-2-butene peroxodisulfate. Chemoselective oxidation of 3,4-dihydropyrimidin in the presence of other oxidizable functional groups was also achieved by this reagent.

• Korean Chemical Engineering Research
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• v.53 no.6
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• pp.824-830
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• 2015

The influence of phosphorous precursors, $NH_4H_2PO_4$, $(NH_4)_2HPO_4$, $H_3PO_4$, $(C_2H_5)_3PO_4$, and $P_2O_5$, on the catalytic performance of the $BiFe_{0.65}MoP_{0.1}$ catalysts in the oxidative dehydrogenation of 1-butene to 1,3-butadiene was studied. The catalysts were characterized by XRD, $N_2$-sorption, ICP, SEM and TPRO analyses. It was not observed big difference on the physical properties of catalysts in accordance with used different phosphorous precursors, however, the catalytic performance was largely depended on the nature of the phosphorous precursors. Of various precursors, the $BiFe_{0.65}MoP_{0.1}$ oxide catalyst, which was prepared from a phosphoric acid precursor, showed the best catalytic performance. Conversion and yield to butadiene of the catalyst showed 79.5% and 67.7%, respectively, after 14 h on stream. The cation of phosphorous precursors was speculated to affect the lattice structure of the catalysts during catalyst preparation and this difference was influenced on the re-oxidation ability of the catalysts. Based on the results of TPRO, it was proposed that the catalytic performance could be correlated with re-oxidation ability of the catalysts.