کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
44545 | 46041 | 2006 | 11 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Hydrogen production by partial oxidation of methanol over gold catalysts supported on TiO2-MOx (M = Fe, Co, Zn) composite oxides Hydrogen production by partial oxidation of methanol over gold catalysts supported on TiO2-MOx (M = Fe, Co, Zn) composite oxides](/preview/png/44545.png)
Hydrogen production by partial oxidation of methanol (POM) has been investigated over Au/TiO2-MOx (M = Fe, Co and Zn) catalysts in the temperature range of 423–548 K. The catalysts were characterized by ICP, BET, XRD, TEM and XPS analyses. The XRD analysis confirms the desired structure and phase purity of Fe2O3, Co3O4, ZnO and TiO2 samples and the presence of gold in these materials. TEM observations show that the gold particles are stabilized against sintering during calcination and after catalytic tests, in the presence of MOx in Au/TiO2 catalysts. The XPS analysis detects the existence of metallic gold (Au0), non-metallic gold (Auδ+) and Au2O3 species in the uncalcined catalyst samples both before and after reaction, and the existence of metallic gold (Au0) and Au2O3 species in the calcined catalyst samples. The catalytic activity of Au/TiO2 for the POM reaction to produce hydrogen is improved by using additional support (MOx), probably due to a combination of factors, such as increasing the mobility of the lattice oxygen, maintaining the adequate oxidation state of the active gold particles and controlling the sintering of gold particles. Therefore, MOx can act as a structural promoter and/or as a cocatalyst. The most active catalyst is Au/TiO2-Fe2O3. Although Fe2O3 in Au/TiO2 catalysts increases the catalytic activity, a surfeit of Fe2O3 lowers the activity for hydrogen formation. Calcination of the catalyst samples results in a decrease of the catalytic activity. The sample dried at 373 K in air exhibits the highest activity for POM reaction. Both methanol conversion and hydrogen selectivity are increased with increase in reaction temperature. The reaction pathway is suggested to consist of consecutive methanol combustion, partial oxidation, steam reforming and decomposition. CO produced by methanol decomposition and/or by reverse water gas shift is subsequently transformed into CO2 and H2 by the water gas shift and/or CO oxidation.
Journal: Applied Catalysis A: General - Volume 302, Issue 2, 11 April 2006, Pages 157–167