Abstract

The ageing effect induced by S-compounds over 2%Pd/CeO 2·2ZrO 2, 2%Pd/LaMnO 3·2ZrO 2 and 2%Pd/BaCeO 3·2ZrO 2 catalysts for CH 4 combustion was investigated; S-compounds are in fact added as odorants in the natural gas network for safety purposes. Pd-based catalysts were prepared by solution combustion synthesis (SCS), starting from metal nitrates/glycine mixtures. Basic characterization (XRD, BET, FESEM analysis), FT–IR studies and catalytic activity tests were performed on powders and after accelerated ageing carried out up to 2 weeks (hydro-thermal treatment at 900 °C under a flow rate with typical domestic boiler exhaust gas composition, 9% CO 2, 18% H 2O, 2% O 2 in N 2, containing also 200 ppmv of SO 2 to emphasize any poisoning effect). Over fresh catalysts, IR analysis of CO adsorption evidenced the formation of highly dispersed Pd metal clusters and Pd ions. With ageing, 2%Pd/CeO 2·2ZrO 2 increased its CH 4 combustion half-conversion temperature ( T 50, regarded as an index of catalytic activity) from 382 °C—recorded for fresh sample—to 421 °C, attained with the same sample aged two weeks. An unexpected improvement was found instead in the overall performance of 2%Pd/LaMnO 3·2ZrO 2 and 2%Pd/BaCeO 3·2ZrO 2: the T 50 in fact lowered from 570 to 450 °C for the first one, and from 512 to 443 °C for the second one, after two weeks ageing. S-hydro-thermal treatment provoked bulk and surface sulfates formation on all aged samples, with a concentration increasing with the exposure time. Prevailing ageing mechanisms seemed to be Pd metallic clusters coalescence, detected over the Ce–Zr system, and surface-bulk sulfates formation, the latter destroying the initial crystallographic structure. In 2%Pd/LaMnO 3·ZrO 2 and 2%Pd/BaCeO 3·ZrO 2 powders the amount of the perovskite phase strongly decreased during ageing, in favor of the formation of bulk sulfate and of oxides.

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.