TY - JOUR
T1 - Sonochemical oxidation of carbon disulfide in aqueous solutions
T2 - Reaction kinetics and pathways
AU - Adewuyi, Yusuf G.
AU - Appaw, Collins
PY - 2002/10/2
Y1 - 2002/10/2
N2 - The kinetics of sonochemical oxidation of CS2 and the effects of process parameters (e.g., concentration, pH, temperature, ultrasonic intensity, irradiation medium, dissolved gas and time, etc.) on the degradation rates and product distributions were studied in a batch reactor at 20 kHz. Sonochemical oxidation was found to decrease with an increase in the solution temperature, and the reaction rate order was dependent on the temperature (T) range studied: zero-order at T ≥ 10°C [with rate constants of (0.66-3.68) × 10-5 M min-1] and first-order at T ≤ 5°C (with rate constants of 0.037-0.266 min-1). From Arrhenius law, k = A exp(EA/RT), the activation energy, EA, for the zero-order degradation of CS2 in the presence of air as the irradiating gas was found to be 7.2 kJ/mol at the higher temperatures compared to 28.7 kJ/mol for the first-order degradation at the lower temperatures. Sonochemical oxidation pathways leading to sulfate formation are discussed. The results of this study suggest that the ultrasonic degradation of CS2 might provide an environmentally conscious method for the control of this hazardous pollutant in industrial wastewater.
AB - The kinetics of sonochemical oxidation of CS2 and the effects of process parameters (e.g., concentration, pH, temperature, ultrasonic intensity, irradiation medium, dissolved gas and time, etc.) on the degradation rates and product distributions were studied in a batch reactor at 20 kHz. Sonochemical oxidation was found to decrease with an increase in the solution temperature, and the reaction rate order was dependent on the temperature (T) range studied: zero-order at T ≥ 10°C [with rate constants of (0.66-3.68) × 10-5 M min-1] and first-order at T ≤ 5°C (with rate constants of 0.037-0.266 min-1). From Arrhenius law, k = A exp(EA/RT), the activation energy, EA, for the zero-order degradation of CS2 in the presence of air as the irradiating gas was found to be 7.2 kJ/mol at the higher temperatures compared to 28.7 kJ/mol for the first-order degradation at the lower temperatures. Sonochemical oxidation pathways leading to sulfate formation are discussed. The results of this study suggest that the ultrasonic degradation of CS2 might provide an environmentally conscious method for the control of this hazardous pollutant in industrial wastewater.
UR - https://www.scopus.com/pages/publications/0037009815
U2 - 10.1021/ie020069a
DO - 10.1021/ie020069a
M3 - Article
SN - 0888-5885
VL - 41
SP - 4957
EP - 4964
JO - Industrial and Engineering Chemistry Research
JF - Industrial and Engineering Chemistry Research
IS - 20
ER -