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Pt-CeO2-ZrO2/MgO (Pt-CZ/MgO) catalysts with 0.8 wt% Pt, 3.0 wt% CeO2 and 3.0 wt% ZrO2 were prepared by wet impregnation method. Support MgO was obtained using ion exchange resin method or using commercial MgO. XRD, BET, SEM, TEM, DTA-TG and CO2-TPD were used to characterize the catalysts. CH4-CO2 reforming to synthesis gas (syngas) was performed to test the catalytic behavior of the catalysts. The catalyst Pt-CZ/MgO-IE(D) prepared using ion exchange resin exhibits more regular structure, smaller and more unique particle sizes, and stronger basicity than the catalyst Pt-CZ/MgO prepared from commercial MgO. At 1073 K and atmospheric pressure, Pt-CZ/MgO-IE(D) catalyst has a higher activity and greater stability than Pt-CZ/MgO catalyst for CH4-CO2 reforming reaction at high gas hourly space velocity of 36000 mL/(g·h) with a stoichiometric feed of CH4 and CO2. Activity measurement and characterization results demonstrate that modification of the support using ion exchange resin method can promote the surface structural property and stability, therefore enhancing the activity and stability for CH4-CO2 reforming reaction.
Pt-CeO2-ZrO2 / MgO (Pt-CZ / MgO) catalysts with 0.8 wt% Pt, 3.0 wt% CeO2 and 3.0 wt% ZrO2 were prepared by wet impregnation method. . CH 4 -CO 2 reforming to synthesis gas (syngas) was performed to test the catalytic behavior of the catalysts. The catalyst Pt-CZ / MgO-IE (D) prepared using ion exchange resin exhibits more regular structure, smaller and more unique particle sizes, and stronger basicity than the catalyst Pt-CZ / MgO prepared from commercial MgO. At 1073 K and atmospheric pressure, Pt-CZ / MgO-IE (D) catalyst has a higher activity and greater stability than Pt-CZ / MgO catalyst for CH4-CO2 reforming reaction at high gas hourly space velocity of 36000 mL / (g · h) with a stoichiometric feed of CH4 and CO2 Activity measurement and characterization results demonstrate that modification of the support using ion exchange resin method can promote the surface structural property and stability, therefore enhancing the activity and stability for CH4-CO2 reforming reaction.