Direct synthesis of hydrocarbons through carbon dioxide hydrogenation was investigated over hybrid catalysts composed of methanol synthesis catalysts (Cu/ZnO/ZrO, and Cu/ZnO/Al,O,) and molecular sieves (H-ZSM-5, SAPO-5 and SAPO-44). It was found that the hybrid catalyst with SAPO-5 or SAP044 was eff
Hydrogenation of carbon dioxide to C1-C7 hydrocarbons via methanol on composite catalysts
β Scribed by Tomoyuki Inui; Kazuichi Kitagawa; Tatsuya Takeguchi; Takashi Hagiwara; Yoshinori Makino
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 595 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0926-860X
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β¦ Synopsis
Hydrocarbon synthesis from C02 and H2, via methanol, was studied. Composite catalysts consisting of a low-temperature methanol synthesis catalyst and typical H-ZSM-5 were adopted. Syngas conversion was studied for comparison. Mixing H-ZSM-5 with the methanol synthesis catalyst promoted methanol conversion to hydrocarbons. It markedly affected the rate of syngas conversion, since the equilibrium between syngas and methanol was shifted. However, the rate of CO2 hydrogenation was not affected. For this reason, it was considered that methanol was formed via CO as the intermediate in C02 hydrogenation on the composite catalyst, and consequently the selectivity to methanol was considerably low. There%re. the effect of H-ZSM-5 was reduced. Nevertheless, hydrocarbons containing 71.8% C~-C7 in addition to 28.2% methane could be obtained on a catalyst of mixed Pd-Na-modified Cu Cr-Zn oxides and the H-ZSM-5.
π SIMILAR VOLUMES
The effect of Pd on a Cu/ZnO/A1203 catalyst for methanol synthesis from CO2/H 2 has been investigated. Activities of impregnated catalysts and physical mixtures were studied in an internal recycle reactor under 5 MPa, 250Β°C and a range of conversions. In all cases, the promotion of methanol producti
Composite catalysts containing zeolites and Na-rich Fe-Cu Fischer-Tropsch catalysts were studied for the hydrogenation of carbon dioxide at 2508C. Sodium migration from the surface of the F-T catalyst to the zeolite via solid-solid reaction seemed to change the acidity of the zeolite and the reducti