Influence of the Titanium Content in the Ti-MCM-41 Catalyst on the Course of the α-Pinene Isomerization Process
Autor: | Joanna Sreńscek-Nazzal, Jadwiga Tołpa, Zvi C. Koren, Agnieszka Wróblewska, Piotr Miądlicki, Beata Michalkiewicz |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
chemistry.chemical_element
02 engineering and technology 010402 general chemistry lcsh:Chemical technology 01 natural sciences Catalysis isomerization law.invention lcsh:Chemistry Adsorption MCM-41 law Desorption Ti-MCM-41 natural compounds lcsh:TP1-1185 Physical and Theoretical Chemistry Crystallization camphene green chemistry Mesoporous silica 021001 nanoscience & nanotechnology 0104 chemical sciences chemistry lcsh:QD1-999 α-pinene limonene 0210 nano-technology Isomerization Nuclear chemistry Titanium |
Zdroj: | Catalysts, Vol 9, Iss 5, p 396 (2019) Catalysts Volume 9 Issue 5 |
ISSN: | 2073-4344 |
Popis: | Titanium-containing mesoporous silica catalysts with different Ti contents were prepared by the sol&ndash gel method, whereby the molar ratios of silicon to titanium in the crystallization gel amounted to, respectively, 40:1, 30:1, 20:1 and 10:1. The produced Ti-MCM-41 materials were characterized by the following instrumental methods: XRD, UV-Vis, FT-IR, SEM, and XRF. Textural parameters were also determined for these materials by means of the N2 adsorption/desorption method. The activities of these catalysts were investigated in the &alpha pinene isomerization process. The most active catalyst was found to be the material with the molar ratio of Si:Ti equal to 10:1, which contained 12.09 wt% Ti. This catalyst was used in the extended studies on the &alpha pinene isomerization process, and the most favorable conditions for this reaction were found to be temperature of 160 ° C, reaction time of 7 h, with the catalyst composition of 7.5 wt% relative to &alpha pinene. These studies showed that the most active catalyst, at the best reaction conditions, allowed for the attainment of 100% conversion of &alpha pinene over a period of 7 h. After this time the selectivities (in mol%) of the main products were as follows: camphene (35.45) and limonene (21.32). Moreover, other products with lower selectivities were formed: &gamma terpinene (4.38), &alpha terpinene (8.12), terpinolene (11.16), p-cymene (6.61), and &alpha phellandrene (1.58). |
Databáze: | OpenAIRE |
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