Abstract:Elemental sulfur recovery from SO2-containing gas streams is highly attractive as it produces a saleable product and no waste to dispose of. However, commercially available schemes are complex and involve multi-stage reactors, such as, most notably in the Resox(reduction of SO2 with coke) and Claus plants(reaction of SO2 with H2S over catalyst). This project will investigate a cerium oxide catalyst for the single-stage selective reduction of SO2 to elemental sulfur by a reductant, such as carbon monoxide. Ceri… Show more
“…However, in the case of 5CuC-100, 5CuC-200 and 5CuC-300, peak temperatures of a peak shifted to lower temperatures from 163 to 156 C and H 2 consumptions of b peak increased from 336 to 349 mmol g À1 cat . Obviously, the lower the peak temperatures of a peak were, the higher the activity of CuO2CeO 2 catalysts in preferential oxidation of CO was [18]. But H 2 consumptions of b peak had a contrary trend with the activity of CuO2CeO 2 catalysts, indicating that b peak played a slight role on the catalytic performance of CuO2CeO 2 catalysts [19].…”
Section: Article In Pressmentioning
confidence: 99%
“…The PROX may be the most suitable method to reduce the amount of carbon monoxide to a level for use in electrochemical fuel cells [5]. The catalysts employed in the PROX include noble and nonnoble metal catalysts, while CuO2CeO 2 catalysts show a catalytic performance as well as, if not better than, noble metal catalysts [6][7][8][9]. Generally, preparation methods have a strong influence on the catalytic performance of CuO2CeO 2 catalysts [9,10].…”
“…However, in the case of 5CuC-100, 5CuC-200 and 5CuC-300, peak temperatures of a peak shifted to lower temperatures from 163 to 156 C and H 2 consumptions of b peak increased from 336 to 349 mmol g À1 cat . Obviously, the lower the peak temperatures of a peak were, the higher the activity of CuO2CeO 2 catalysts in preferential oxidation of CO was [18]. But H 2 consumptions of b peak had a contrary trend with the activity of CuO2CeO 2 catalysts, indicating that b peak played a slight role on the catalytic performance of CuO2CeO 2 catalysts [19].…”
Section: Article In Pressmentioning
confidence: 99%
“…The PROX may be the most suitable method to reduce the amount of carbon monoxide to a level for use in electrochemical fuel cells [5]. The catalysts employed in the PROX include noble and nonnoble metal catalysts, while CuO2CeO 2 catalysts show a catalytic performance as well as, if not better than, noble metal catalysts [6][7][8][9]. Generally, preparation methods have a strong influence on the catalytic performance of CuO2CeO 2 catalysts [9,10].…”
“…12 They concluded that only a small amount of copper is necessary to promote the CO oxidation. The excess of copper forms bulk CuO particles, which contributes little to the catalyst activity.…”
X-ray photoelectron spectroscopy ͑XPS͒, x-ray diffraction ͑XRD͒, and x-ray absorption spectroscopy ͑XAS͒ techniques have been applied to characterize the surface composition and structure of a series of CuO-TiO 2 -CeO 2 catalysts. For a small loading of cerium, ceria was mainly dispersed on the titania surface and a minor amount of CeO 2 crystallite appeared. At higher loading of cerium, the CeO 2 phase increased and the atomic Ce/Ti ratio values were smaller than the nominal composition, as a consequence of cerium agglomeration. This result suggests that only a fraction of cerium can be spread on the titania surface. For titanium-based mixed oxide, we observed that cerium is found as Ce 3ϩ uniquely on the surface. The atomic Cu/͑CeϩTi͒ ratio values showed no influence from cerium concentration on the dispersion of copper, although the copper on the surface was shown to be dependent on the cerium species. For samples with a high amount of cerium, XPS analysis indicated the raise of second titanium species due cerium with spin-orbit components at higher binding energies than those presented by Ti 4ϩ in a tetragonal structure. The structural results obtained by XAS are consistent with those obtained by XRD and XPS.
“…An exponential growth of published reports on gold and the plethora of the reactions it catalyzes has taken place over the last 25 years. This system was soon followed by a detailed structural and kinetic study by Liu and Flytzani-Stephanopoulos [54]. The CO oxidation reaction was first studied on Au/CeO 2 by Hoflund and co-workers [67].…”
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