Abstract

AbstractPromoting the activity of catalyst, achieving high CO2 conversion and increasing light olefins yield are important in CO2 hydrogenation to olefin. Herein, SiO2 was doped in CuO‐ZnO‐ZrO2 to form multi‐oxides of CuO‐ZnO‐ZrO2‐SiO2 by co‐precipitation method, and the multi‐oxides was mixed with SAPO‐34 molecular sieves mechanically to form a composite catalyst of CuO‐ZnO‐ZrO2‐SiO2/SAPO‐34. Compared with CuO‐ZnO‐ZrO2, doping of SiO2 increases the dispersion and thermal stability of metal oxides, provides more sites for CO2 activated, and delays the aggregation of metal particles at higher temperature. Doped SiO2 can also adsorb the water from hydrogenation process to improve the olefins yield and hinder the formation of CO from reverse water gas shift. Thus, under the condition of reaction temperature at 420 °C, pressure of 3.0 MPa, space velocity of 1800 mL gcat−1 h−1, CO2/H2 (molar ratio) of 1 : 3 and the mass ratio of CuO‐ZnO‐ZrO2‐SiO2 (containing 8 % SiO2) to SAPO‐34 of 1 : 1, the direct CO2 hydrogenation to light olefins on CuO‐ZnO‐ZrO2‐SiO2/SAPO‐34 shows that the conversion of CO2 is 53.9 % and the selectivity of light olefins is 52.9 %, while the CO selectivity is only 13.6 %.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.