TY - JOUR
T1 - Surface-selective infiltration of thin-film catalyst into microchannel reactors
AU - Chen, H.
AU - Bednarova, L.
AU - Besser, R. S.
AU - Lee, W. Y.
PY - 2005
Y1 - 2005
N2 - A thin-film Pt/Al2O3 catalyst was synthesized by a sol-gel synthesis method with hydrogen hexachloroplatinate hydrate and aluminum isopropoxide as precursors in a water-based solvent. The catalyst contained ∼5 nm Pt particles dispersed on Al2O3 support, which was mostly amorphous with a specific surface area of 400-450 m2/g and a pore size distribution in the range of 2-8 nm. For uniform infiltration of the solgel catalyst precursor into the microchannel of Si-based reactors, a hydrophobic film was applied to the top surface of the reactors while reactive ion etched microchannel surface of the reactors remained hydrophilic. Under these surface conditions, the catalyst precursor infiltrated selectively into the microchannel without spilling over to the reactor surface. In comparison to other infiltration methods, this surface-selective approach provided an effective means of precisely controlling the amount of catalyst loaded into the reactors and keeping the reactor surface clean for subsequent sealing via anodic bonding. However, as delamination occurred preferentially at the sharp corners of the microchannel, the thickness of the catalyst layer that could be practically incorporated into the reactors was limited to ∼3 μm.
AB - A thin-film Pt/Al2O3 catalyst was synthesized by a sol-gel synthesis method with hydrogen hexachloroplatinate hydrate and aluminum isopropoxide as precursors in a water-based solvent. The catalyst contained ∼5 nm Pt particles dispersed on Al2O3 support, which was mostly amorphous with a specific surface area of 400-450 m2/g and a pore size distribution in the range of 2-8 nm. For uniform infiltration of the solgel catalyst precursor into the microchannel of Si-based reactors, a hydrophobic film was applied to the top surface of the reactors while reactive ion etched microchannel surface of the reactors remained hydrophilic. Under these surface conditions, the catalyst precursor infiltrated selectively into the microchannel without spilling over to the reactor surface. In comparison to other infiltration methods, this surface-selective approach provided an effective means of precisely controlling the amount of catalyst loaded into the reactors and keeping the reactor surface clean for subsequent sealing via anodic bonding. However, as delamination occurred preferentially at the sharp corners of the microchannel, the thickness of the catalyst layer that could be practically incorporated into the reactors was limited to ∼3 μm.
KW - Microchannel reactor
KW - Sol-gel synthesis
KW - Surface-selective infiltration
KW - Thin-film catalyst
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U2 - 10.1016/j.apcata.2005.03.021
DO - 10.1016/j.apcata.2005.03.021
M3 - Article
AN - SCOPUS:19344365609
SN - 0926-860X
VL - 286
SP - 186
EP - 195
JO - Applied Catalysis A: General
JF - Applied Catalysis A: General
IS - 2
ER -