Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 11Citation - Scopus: 11Effect of Different Acidity Modifications on the Activity and Selectivity on H-Zsm5 Zeolites in N-Butene Isomerization(Springer Verlag, 2014) Kılıç, Emre; Yılmaz, SelahattinH-ZSM-5 was modified by silylation [tetraethylorthosilicate (TEOS) and triaminopropyltriethoxysilane], alkali (NaOH), acid (HCl) and ammoniumhexafluorosilicate (AHFS) treatments. The parent and modified zeolite forms were tested in n-butene isomerization. Modifications affected total acidities, the strength of the acid sites, pore sizes and surface areas of the H-ZSM-5 differently. The modifications decreased the conversion obtained by the parent catalyst. TEOS and alkali modifications did not promote formation of isobutene. Pre-alkali treatment before acid treatment increased selectivity to isobutene from 56.0 to 66.7 %, while conversion changed a little, it dropped from 52 to 50 %. AHFS modification provided the highest enhancement in selectivity to isobutene (87.5 %) for which n-butene conversion was dropped by about 10 % compared to H-ZSM-5. This was attributed to a slight modification of the pore size and to the reduction in strong and weak acid sites and generation of new Lewis acid sites.Article Citation - WoS: 4Citation - Scopus: 4Hzsm-5 and H-Ferrierite Acidity Modification by Silylation and Their Activities in N-Butene Isomerisation(Walter de Gruyter GmbH, 2010) Kılıç, Emre; Yılmaz, SelahattinH-ZSM5 and H-Ferrierite acidities were modified by chemical liquid deposition using tetraethylorthosilicate (TEOS), silicontetratchloride (SiCl4) and triaminopropyltriethoxysilane (3-APTES). All depositions were carried out at room temperature for deposition times of 0.5 and 1 h. Reaction tests were performed in a tubular quartz fixed bed reactor at 375°C for weight hour space velocities of 22 h-1. Surface area and pore volume of the catalysts were decreased upon modifications. The least modification of acidity was achieved by TEOS. However, SiCl4 and 3-APTES deposition modification strongly decreased the number of Bronsted and Lewis acid sites. As the effect of the modification increased, total acidity of the SiCl4 modified catalyst decreased. The catalysts were tested in isomerization of n-butene. Modification decreased the activity of the catalysts, but improvement in selectivity was observed with TEOS deposition. TEOS deposition increased the selectivity of the catalysts; for synthesized H-ZSM5 from 57.95 to 63.74 percent, for commercial H-ZSM5-C from 26.78 to 32.52 percent, and for H-FER from 63.06 to 81.23 percent. However, modification with SiCl4 and 3-APTES decreased both conversion and selectivity of the parent catalysts.