Degradation of antibiotic amoxicillin using 1 x 1 molecular sieve-structured manganese oxide

The kinetics and mechanism ofamoxicillin (AMO) degradation using a 1 x 1 molecular sieve-structured manganese oxide (MnO2) was studied. The presence of the buffer solution (i.e., NaHCO3, NaH2PO4 and KH2PO4) diminished AMO binding to MnO2, thus reducing AMO degradation in the pretest; therefore, all...

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Veröffentlicht in:Environmental technology. - 1998. - 34(2013), 13-16 vom: 17. Juli, Seite 2443-51
1. Verfasser: Kuan, Wen-Hui (VerfasserIn)
Weitere Verfasser: Hu, Ching-Yao, Liu, Bin-Sheng, Tzou, Yu-Min
Format: Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Environmental technology
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Anti-Bacterial Agents Manganese Compounds Oxides Water Pollutants, Chemical manganese oxide 64J2OA7MH3 Amoxicillin 804826J2HU
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520 |a The kinetics and mechanism ofamoxicillin (AMO) degradation using a 1 x 1 molecular sieve-structured manganese oxide (MnO2) was studied. The presence of the buffer solution (i.e., NaHCO3, NaH2PO4 and KH2PO4) diminished AMO binding to MnO2, thus reducing AMO degradation in the pretest; therefore, all other experiments in this study were conducted without the addition of a buffer. Third-order rate constants, second-order on AMO and first-order on MnO2 increased with elevating pH level (2.81-7.23) from 0.54 to 9.17 M(-2) s(-1), and it decreased to 4.27 M(-2) s(-1) at pH 8.53 beyond the pk(a2) of AMO (7.3). The dissolution of the MnO2 suspension with and without AMO exhibited a similar trend; that is, Mn2+ concentration increased with decreasing pH. However, the dissolution of MnO2 with AMO was greater than that without AMO, except for the reaction occurring at pH 8.53, partially indicating that MnO2 acts as an oxidant in AMO degradation. The preliminary chromatogram data display different products with varying pH reaction s, implying that AMO elimination using this 1 x 1 molecular sieve-structured MnO2 is by adsorption as well as oxidative degradation. A complementary experiment indicates that the amount of oxidatively degraded AMO increases substantially from 65.5% at 4 h to 95% at 48 h, whereas the AMO adsorbed onto MnO2 decreases slightly from 4.5% at4 h to 2.4% at 48 h. The oxidative degradation accounted for more AMO removal than adsorption over the whole reaction course, indicating that the oxidative reaction of AMO on MnO2 dominated the AMO removal 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a Anti-Bacterial Agents  |2 NLM 
650 7 |a Manganese Compounds  |2 NLM 
650 7 |a Oxides  |2 NLM 
650 7 |a Water Pollutants, Chemical  |2 NLM 
650 7 |a manganese oxide  |2 NLM 
650 7 |a 64J2OA7MH3  |2 NLM 
650 7 |a Amoxicillin  |2 NLM 
650 7 |a 804826J2HU  |2 NLM 
700 1 |a Hu, Ching-Yao  |e verfasserin  |4 aut 
700 1 |a Liu, Bin-Sheng  |e verfasserin  |4 aut 
700 1 |a Tzou, Yu-Min  |e verfasserin  |4 aut 
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