摘要
Electrochemical oxidation reactions of L ascorbic acid(AA) at a copper cobalt hexacyanoferrate modified electrode(CoCuHCF/Pt) in neutral solutions were studied in comparison with that at a bared Pt electrode by in situ FTIR reflection absorption spectroscopy(FTIRRAS). The results indicated that the electrode oxidation of AA at both the electrodes CoCuHCF followed by chemical processes. AA is oxidized to dehydro L ascorbic acid(DHA) followed by a chemical hydration process. At Pt electrode, the DHA underwent hydration reaction to form bicyclic product, which then further was transformed into 2,3 diketogulonic acid and its enol form via an opening of lactone ring. However, at CoCuHCF/Pt electrode, the DHA undergoes ring opening reaction and then degradation reaction.
Electrochemical oxidation reactions of L ascorbic acid(AA) at a copper cobalt hexacyanoferrate modified electrode(CoCuHCF/Pt) in neutral solutions were studied in comparison with that at a bared Pt electrode by in situ FTIR reflection absorption spectroscopy(FTIRRAS). The results indicated that the electrode oxidation of AA at both the electrodes CoCuHCF followed by chemical processes. AA is oxidized to dehydro L ascorbic acid(DHA) followed by a chemical hydration process. At Pt electrode, the DHA underwent hydration reaction to form bicyclic product, which then further was transformed into 2,3 diketogulonic acid and its enol form via an opening of lactone ring. However, at CoCuHCF/Pt electrode, the DHA undergoes ring opening reaction and then degradation reaction.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
2002年第8期1498-1500,共3页
Chemical Journal of Chinese Universities
基金
中国科学技术大学高水平大学建设重点科研项目 (批准号 :KY2 2 16)资助
