TY - JOUR
T1 - Kinetics and modeling of the removal of nitric oxide by aqueous sodium persulfate simultaneously activated by temperature and Fe2+
AU - Adewuyi, Yusuf G
AU - Khan, Md A.
AU - Sakyi, Nana Y.
PY - 2014/1/15
Y1 - 2014/1/15
N2 - The chemistry and kinetics of NO removal by aqueous solutions of sodium persulfate (Na2S2O8) simultaneously activated by temperature and Fe2+ were studied in a bubble reactor. Reaction pathways were proposed and a mathematical model utilizing the pseudo-steady-state-approximation technique and film theory of mass transfer were developed. The model was solved numerically using the fourth order Runge-Kutta method in Matlab to obtain species concentrations; correlate experimental data; and estimate mass transfer and kinetic rate parameters. The model was used to investigate the effects of Na2S2O 8 (0.01-0.2 M), Fe2+ (0-0.1 M), gas-phase NO (500-1000 ppm) concentrations and temperatures (23-90 C), and is a follow-up to an experimental study, which demonstrated that Fe2+ activation further improved NO conversion by ∼10% at all temperatures. The model results, which appeared to fit those of the experiments remarkably well, were discussed and predicted kinetic data compared with available literature values. © 2013 American Chemical Society.
AB - The chemistry and kinetics of NO removal by aqueous solutions of sodium persulfate (Na2S2O8) simultaneously activated by temperature and Fe2+ were studied in a bubble reactor. Reaction pathways were proposed and a mathematical model utilizing the pseudo-steady-state-approximation technique and film theory of mass transfer were developed. The model was solved numerically using the fourth order Runge-Kutta method in Matlab to obtain species concentrations; correlate experimental data; and estimate mass transfer and kinetic rate parameters. The model was used to investigate the effects of Na2S2O 8 (0.01-0.2 M), Fe2+ (0-0.1 M), gas-phase NO (500-1000 ppm) concentrations and temperatures (23-90 C), and is a follow-up to an experimental study, which demonstrated that Fe2+ activation further improved NO conversion by ∼10% at all temperatures. The model results, which appeared to fit those of the experiments remarkably well, were discussed and predicted kinetic data compared with available literature values. © 2013 American Chemical Society.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84892706446&origin=inward
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=84892706446&origin=inward
U2 - 10.1021/ie402801b
DO - 10.1021/ie402801b
M3 - Article
SN - 0888-5885
VL - 53
SP - 828
EP - 839
JO - Industrial and Engineering Chemistry Research
JF - Industrial and Engineering Chemistry Research
IS - 2
ER -