TY - JOUR
T1 - Insights into the redox kinetics of vanadium substituted heteropoly acids through liquid core waveguide membrane microreactor studies
AU - Ponce, Sebastian
AU - Trabold, Michael
AU - Drochner, Alfons
AU - Albert, Jakob
AU - Etzold, Bastian J.M.
N1 - Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - A liquid core waveguide membrane microreactor is a novel concept that allows in situ spectroscopy to be carried out in an optical microreactor, while enabling a very high gas-to-liquid mass transfer. The potential of this reactor concept to derive kinetics in gas/liquid reactions is demonstrated using the heteropoly acids catalyzed oxidation of biomass to formic acid (the ‘OxFA process’). For vanadium-substituted, Keggin-type heteropoly acids, the kinetics of the reduction and reoxidation step of the catalyst cycle was deduced using in situ UV/Vis spectroscopy. Reduction was studied from 40 to 80 °C: a strong dependency of the reduction kinetics was deduced. In combination with additional cyclic voltammetry and EPR characterization, it can be assumed that two active centers promote this reaction, while the existence and proportions of both types depends on the degree of vanadium substitution. The rapid mass transfer allowed transient response experiments to be carried out for the reoxidation step, which was studied up to 150 °C. Switching from anaerobic to aerobic conditions, an even stronger dependency of the reoxidation kinetics on the degree of vanadium substitution was revealed.
AB - A liquid core waveguide membrane microreactor is a novel concept that allows in situ spectroscopy to be carried out in an optical microreactor, while enabling a very high gas-to-liquid mass transfer. The potential of this reactor concept to derive kinetics in gas/liquid reactions is demonstrated using the heteropoly acids catalyzed oxidation of biomass to formic acid (the ‘OxFA process’). For vanadium-substituted, Keggin-type heteropoly acids, the kinetics of the reduction and reoxidation step of the catalyst cycle was deduced using in situ UV/Vis spectroscopy. Reduction was studied from 40 to 80 °C: a strong dependency of the reduction kinetics was deduced. In combination with additional cyclic voltammetry and EPR characterization, it can be assumed that two active centers promote this reaction, while the existence and proportions of both types depends on the degree of vanadium substitution. The rapid mass transfer allowed transient response experiments to be carried out for the reoxidation step, which was studied up to 150 °C. Switching from anaerobic to aerobic conditions, an even stronger dependency of the reoxidation kinetics on the degree of vanadium substitution was revealed.
KW - Anaerobic aerobic oxidation
KW - Biomass oxidation
KW - Heteropoly acids
KW - Membrane microreactors
KW - Optical microreactors
KW - OxFA process
UR - http://www.scopus.com/inward/record.url?scp=85062722342&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2019.03.103
DO - 10.1016/j.cej.2019.03.103
M3 - Artículo
AN - SCOPUS:85062722342
SN - 1385-8947
VL - 369
SP - 443
EP - 450
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -