The SnO 2 with a particle size of about 300 nm instead of Ni is used in this study to overcome rapid catalytic deactivation by the formation of a NiAl 2 O 4 spinal structure on the conventional Ni/γ-Al 2 O 3 catalyst and simultaneously impregnated the catalyst with potassium (K). The SnO 2 -K 2 O impregnated Zeolite Y catalyst (SnO 2 -K 2 O/ZY) exhibited significantly higher ethanol reforming reactivity that that achieved with SnO 2 100 and SnO 2 30 wt %/ZY catalysts. The main products from ethanol steam reforming (ESR) over the SnO 2 -K 2 O/ ZY catalyst were H 2 , CO 2 , and CH 4 , with no evidence of any CO molecule formation. The H 2 production and ethanol conversion were maximized at 89% and 100%, respectively, over SnO 2 30 wt %-K 2 O 3.0 wt %/ZY at 600 o C for 1 h at a CH 3 CH 2 OH:H 2 O ratio of 1:1 and a gas hourly space velocity (GHSV) of 12,700 h −1. No catalytic deactivation occurred for up to 73 h. This result is attributable to the easier and weaker of reduction of Sn components and acidities over SnO 2 -K 2 O/ZY catalyst, respectively, than those of Ni/γ-Al 2 O 3 catalysts.
Nanoporous structured tin dioxide (SnO 2 ) is characterized and its application in the photocatalytic destruction of endocrine, Bisphenol A, is examined. Transmission electron microscopy (TEM) reveals irregularly shaped nanopores of size 2.0-4.5 nm. This corresponds to the result of an average nanopore distribution of 4.5 nm, as determined by Barret-Joyner-Halenda (BJH) plot from the isotherm curve. The photoluminescence (PL) curve, corresponding to the recombination between electron and hole, largely decreases in the TiO 2 /nanoporous SnO 2 composite. Finally, a synergy effect between TiO 2 and porous SnO 2 is exhibited in photocatalysis: the photocatalytic destruction of Bisphenol A is improved by combining the nanoporous structured SnO 2 with TiO 2 , and 75% decomposition of 10.0 ppm of Bisphenol A is achieved after 24 h.
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