Route of electrochemical oxidation of the antibiotic sulfamethoxazole on a mixed oxide anode

The appearance of pharmaceutical compounds and their bioactive transformation products in aquatic environments is becoming an issue of increasing concern. In this study, the electrochemical oxidation of the widely used antibiotic sulfamethoxazole (SMX) was investigated using a commercial mixed oxide...

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Veröffentlicht in:Environmental science and pollution research international 2015-10, Vol.22 (19), p.15004-15015
Hauptverfasser: Hussain, Sajjad, Gul, Saima, Steter, Juliana R., Miwa, Douglas W., Motheo, Artur J.
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container_issue 19
container_start_page 15004
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creator Hussain, Sajjad
Gul, Saima
Steter, Juliana R.
Miwa, Douglas W.
Motheo, Artur J.
description The appearance of pharmaceutical compounds and their bioactive transformation products in aquatic environments is becoming an issue of increasing concern. In this study, the electrochemical oxidation of the widely used antibiotic sulfamethoxazole (SMX) was investigated using a commercial mixed oxide anode (Ti/Ru 0.3 Ti 0.7 O 2 ) and a single compartment filter press-type flow reactor. The kinetics of SMX degradation was determined as a function of electrolyte composition, applied current density, and initial pH. Almost complete (98 %) degradation of SMX could be achieved within 30 min of electrolysis in 0.1 mol L −1 NaCl solution at pH 3 with applied current densities ≥20 mA cm −2 . Nine major intermediates of the reaction were identified by LC-ESI-Q-TOF-MS (e.g., C 6 H 9 NO 2 S ( m / z  = 179), C 6 H 4 NOCl ( m / z  = 141), and C 6 H 6 O 2 ( m / z  = 110)). The degradation followed various routes involving cleavage of the oxazole and benzene rings by hydroxyl and/or chlorine radicals, processes that could occur before or after rupture of the N-S bond, followed by oxidation of the remaining moieties. Analysis of the total organic carbon content revealed that the antibiotic was partially mineralized under the conditions employed and some inorganic ions, including NO 3 − and SO 4 2− , could be identified. The results presented herein demonstrate the efficacy of the electrochemical process using a Ti/Ru 0.3 Ti 0.7 O 2 anode for the remediation of wastewater containing the antibiotic SMX.
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In this study, the electrochemical oxidation of the widely used antibiotic sulfamethoxazole (SMX) was investigated using a commercial mixed oxide anode (Ti/Ru 0.3 Ti 0.7 O 2 ) and a single compartment filter press-type flow reactor. The kinetics of SMX degradation was determined as a function of electrolyte composition, applied current density, and initial pH. Almost complete (98 %) degradation of SMX could be achieved within 30 min of electrolysis in 0.1 mol L −1 NaCl solution at pH 3 with applied current densities ≥20 mA cm −2 . Nine major intermediates of the reaction were identified by LC-ESI-Q-TOF-MS (e.g., C 6 H 9 NO 2 S ( m / z  = 179), C 6 H 4 NOCl ( m / z  = 141), and C 6 H 6 O 2 ( m / z  = 110)). The degradation followed various routes involving cleavage of the oxazole and benzene rings by hydroxyl and/or chlorine radicals, processes that could occur before or after rupture of the N-S bond, followed by oxidation of the remaining moieties. Analysis of the total organic carbon content revealed that the antibiotic was partially mineralized under the conditions employed and some inorganic ions, including NO 3 − and SO 4 2− , could be identified. 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In this study, the electrochemical oxidation of the widely used antibiotic sulfamethoxazole (SMX) was investigated using a commercial mixed oxide anode (Ti/Ru 0.3 Ti 0.7 O 2 ) and a single compartment filter press-type flow reactor. The kinetics of SMX degradation was determined as a function of electrolyte composition, applied current density, and initial pH. Almost complete (98 %) degradation of SMX could be achieved within 30 min of electrolysis in 0.1 mol L −1 NaCl solution at pH 3 with applied current densities ≥20 mA cm −2 . Nine major intermediates of the reaction were identified by LC-ESI-Q-TOF-MS (e.g., C 6 H 9 NO 2 S ( m / z  = 179), C 6 H 4 NOCl ( m / z  = 141), and C 6 H 6 O 2 ( m / z  = 110)). The degradation followed various routes involving cleavage of the oxazole and benzene rings by hydroxyl and/or chlorine radicals, processes that could occur before or after rupture of the N-S bond, followed by oxidation of the remaining moieties. Analysis of the total organic carbon content revealed that the antibiotic was partially mineralized under the conditions employed and some inorganic ions, including NO 3 − and SO 4 2− , could be identified. The results presented herein demonstrate the efficacy of the electrochemical process using a Ti/Ru 0.3 Ti 0.7 O 2 anode for the remediation of wastewater containing the antibiotic SMX.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>26002364</pmid><doi>10.1007/s11356-015-4699-9</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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subjects Anti-Bacterial Agents - chemistry
Antibiotics
Aquatic ecosystems
Aquatic environment
Aquatic Pollution
Aqueous solutions
Atmospheric Protection/Air Quality Control/Air Pollution
Benzene
Chlorine
Drinking water
Earth and Environmental Science
Ecotoxicology
Electrochemistry
Electrodes
Electrolysis
Electrolysis - instrumentation
Electrolytes
Environment
Environmental Chemistry
Environmental Health
Environmental science
Kinetics
Medical research
Organic carbon
Oxidation
Oxidation-Reduction
Oxides - chemistry
Pharmaceuticals
Pollutants
Research Article
Sodium chloride
Studies
Sulfamethoxazole - chemistry
Surface water
Titanium - chemistry
Veterinary medicine
Waste Water - chemistry
Waste Water Technology
Water Management
Water Pollutants, Chemical - chemistry
Water Pollution Control
title Route of electrochemical oxidation of the antibiotic sulfamethoxazole on a mixed oxide anode
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