TY - JOUR
T1 - Continuous Flow Synthesis and Kinetic Study of Diphenyl Sulfoxide in a Microreactor
AU - Zhang, Hongrui
AU - Xu, Feng
AU - Zhou, Xiang
AU - Chen, Zhiquan
AU - Jiang, Juncheng
AU - Fu, Gang
AU - Ni, Lei
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025
Y1 - 2025
N2 - The oxidation of diphenyl sulfide (DPS) by hydrogen peroxide (H2O2) to synthesize diphenyl sulfoxide (DPSO) is extremely exothermic and has a high thermal risk. When thermal runaway happens, it may lead to equipment damage or even explosions. Therefore, in this work, a microreactor was adopted to reduce reaction thermal risk and process conditions were optimized. Phosphotungstic acid (PTA) was used as the catalyst, and the effects of process conditions, including reaction temperature, residence time, catalyst concentration, and molar ratio on the conversion and yield were systematically investigated. The results showed that the DPSO yield could reach up to 84.3% under the condition of 0.75% catalyst loading, 25 min residence time, 70 °C reaction temperature, and H2O2-DPS molar ratio of 2. Then, apparent reaction kinetics were studied, and a kinetic model was established and validated. By varying the initial concentrations of H2O2 and DPS, the reaction was determined to be of second-order, with an activation energy of 57.5 kJ·mol-1 and a pre-exponential factor of 2.96 × 107 mol-1·L·min-1. Furthermore, the temperature distribution along the microreactor was estimated by combining the thermal equilibrium with the reaction kinetics. The results indicated that in a 1/16 in. microreactor, the reaction was nearly isothermal. Temperature distributions were also predicted for microreactors with different diameters and materials. It was demonstrated that the reaction could be safely scaled up to a 3/8 in. microreactor at a reaction temperature of 55 °C, with the maximum temperature rise remaining below 5 °C and no decline in DPSO yield. This study provided a convenient method to guide the safe sizing-up of the reaction in flow reactors.
AB - The oxidation of diphenyl sulfide (DPS) by hydrogen peroxide (H2O2) to synthesize diphenyl sulfoxide (DPSO) is extremely exothermic and has a high thermal risk. When thermal runaway happens, it may lead to equipment damage or even explosions. Therefore, in this work, a microreactor was adopted to reduce reaction thermal risk and process conditions were optimized. Phosphotungstic acid (PTA) was used as the catalyst, and the effects of process conditions, including reaction temperature, residence time, catalyst concentration, and molar ratio on the conversion and yield were systematically investigated. The results showed that the DPSO yield could reach up to 84.3% under the condition of 0.75% catalyst loading, 25 min residence time, 70 °C reaction temperature, and H2O2-DPS molar ratio of 2. Then, apparent reaction kinetics were studied, and a kinetic model was established and validated. By varying the initial concentrations of H2O2 and DPS, the reaction was determined to be of second-order, with an activation energy of 57.5 kJ·mol-1 and a pre-exponential factor of 2.96 × 107 mol-1·L·min-1. Furthermore, the temperature distribution along the microreactor was estimated by combining the thermal equilibrium with the reaction kinetics. The results indicated that in a 1/16 in. microreactor, the reaction was nearly isothermal. Temperature distributions were also predicted for microreactors with different diameters and materials. It was demonstrated that the reaction could be safely scaled up to a 3/8 in. microreactor at a reaction temperature of 55 °C, with the maximum temperature rise remaining below 5 °C and no decline in DPSO yield. This study provided a convenient method to guide the safe sizing-up of the reaction in flow reactors.
KW - microreactor
KW - oxidation
KW - reaction kinetics
KW - temperature distribution
KW - thermal risk
UR - http://www.scopus.com/inward/record.url?scp=105002797438&partnerID=8YFLogxK
U2 - 10.1021/acs.oprd.5c00018
DO - 10.1021/acs.oprd.5c00018
M3 - 文章
AN - SCOPUS:105002797438
SN - 1083-6160
JO - Organic Process Research and Development
JF - Organic Process Research and Development
ER -