The Catalytic Performance of Sol-Gel Alumina Supported Ti-Ce Catalysts for H2S Selective Oxidation to Elemental Sulfur
| Autor: | Nail Yasyerli, Yavuz Yagizatli, H. Mehmet Tasdemir, Sena Yasyerli |
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| Rok vydání: | 2018 |
| Předmět: |
Materials science
General Chemical Engineering chemistry.chemical_element Industrial chemistry 02 engineering and technology 010402 general chemistry 021001 nanoscience & nanotechnology 01 natural sciences Sulfur 0104 chemical sciences Catalysis Cerium chemistry Chemical engineering 0210 nano-technology Titanium Sol-gel |
| Zdroj: | International Journal of Chemical Reactor Engineering. 17 |
| ISSN: | 1542-6580 |
| Popis: | In this study, alumina supported Ti-Ce catalysts (10 % by weight and Ti/Ce molar ratio is 4:1) were prepared by using wet impregnation method and their catalytic activities were tested in H2S selective oxidation to elemental sulfur. The support alumina was synthesized by classical (SGC) and modified (SGM) sol-gel methods. The N2 adsorption-desorption, XRD, XPS, EDS and FTIR techniques were used to characterize the synthesized catalysts. The N2 adsorption-desorption isotherms showed that both catalysts have mesoporous structure. Only γ-Al2O3 crystalline phase together with amorphous structure were observed in the XRD patterns. The pyridine adsorbed FTIR analyzes showed that 10 %Ti-Ce@SGC and 10 %Ti-Ce@SGM catalysts have the same Lewis acidity. The activity tests were carried out at 250 °C and with a stoichiometric feed ratio of O2 to H2S being 0.5 for two different reaction times as 150 and 510 min. Complete conversion of H2S was obtained during 180 min. and 330 min. of reaction time over 10 %Ti-Ce@SGC and 10 %Ti-Ce@SGM, respectively. However, all catalysts showed very high sulfur selectivity. Sulfur deposition was detected over 10 %Ti-Ce@SGC catalyst both 150 and 510 min. of reaction time while it was observed after 510 min. of durability test over 10 %Ti-Ce@SGM catalyst. This can be the reason for the earlier loss of catalytic activity 10 %Ti-Ce@SGC than 10 %Ti-Ce@SGM. |
| Databáze: | OpenAIRE |
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