TY - JOUR
T1 - Ruthenium catalyst on carbon nanofiber support layers for use in silicon-based structured microreactors, Part II: Catalytic reduction of bromate contaminants in aqueous phase
AU - Thakur, D.B.
AU - Tiggelaar, Roald M.
AU - Weber, Y.
AU - Gardeniers, Johannes G.E.
AU - Lefferts, Leonardus
AU - Seshan, Kulathuiyer
PY - 2011
Y1 - 2011
N2 - Catalyst layers were synthesized inside a structured channel of silicon based microreactor and used to remove bromate contaminants in water. It is demonstrated that Ru/CNF based catalyst is active for bromate reduction, resulting in turn over frequencies (TOFs) higher than conventional powdered catalyst, i.e. activated carbon (AC). This enhanced catalytic performance can be attributed to improve mass transfer properties of entangled CNF layers with macroporous (open) structure, which offer enhanced accessibility to all the Ru active sites in contrast to the poor accessibility of active sites in the case of AC support material.
Although promising catalytic activity of Ru/CNF catalyst was observed for bromate reduction, a continuing deactivation was observed during 5 h time on stream operation. A variety of characterization techniques including TEM, XPS, TPR, ICP probed that in addition to catalyst sintering, formation of catalytically inactive Ru(OH)x phase on catalyst surface was an important reason of this deactivation. Use of higher alcohols proved to be beneficial for achieving stability of Ru/CNF catalyst for bromate reduction, however with reduced levels of overall activity
AB - Catalyst layers were synthesized inside a structured channel of silicon based microreactor and used to remove bromate contaminants in water. It is demonstrated that Ru/CNF based catalyst is active for bromate reduction, resulting in turn over frequencies (TOFs) higher than conventional powdered catalyst, i.e. activated carbon (AC). This enhanced catalytic performance can be attributed to improve mass transfer properties of entangled CNF layers with macroporous (open) structure, which offer enhanced accessibility to all the Ru active sites in contrast to the poor accessibility of active sites in the case of AC support material.
Although promising catalytic activity of Ru/CNF catalyst was observed for bromate reduction, a continuing deactivation was observed during 5 h time on stream operation. A variety of characterization techniques including TEM, XPS, TPR, ICP probed that in addition to catalyst sintering, formation of catalytically inactive Ru(OH)x phase on catalyst surface was an important reason of this deactivation. Use of higher alcohols proved to be beneficial for achieving stability of Ru/CNF catalyst for bromate reduction, however with reduced levels of overall activity
KW - IR-94206
KW - METIS-272993
U2 - 10.1016/j.apcatb.2010.12.004
DO - 10.1016/j.apcatb.2010.12.004
M3 - Article
SN - 0926-3373
VL - 102
SP - 243
EP - 250
JO - Applied catalysis B: environmental
JF - Applied catalysis B: environmental
IS - 1-2
ER -