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Effect of calcination temperature on the structure and catalytic performance of copper-ceria mixed oxide catalysts in phenol hydroxylation
被引:80
作者:
Amadine, Othmane
[1
]
Essamlali, Younes
[1
]
Fihri, Aziz
[1
]
Larzek, Mohamed
[3
]
Zahouily, Mohamed
[1
,2
]
机构:
[1] MAScIR Fdn, VARENA Ctr, Rabat Design, Rue Mohamed El Jazouli, Rabat 10100, Morocco
[2] Univ Hassan II Mohammedia, Fac Sci & Tech, URAC 24, Lab Mat Catalyse & Valorisat RessourcesNat, BP 146, Casablanca 20650, Morocco
[3] Mohammed VI Polytech Univ, Lot 660 Hay Moulay Rachid, Ben Guerir 43150, Morocco
来源:
RSC ADVANCES
|
2017年
/
7卷
/
21期
关键词:
INCORPORATED MESOPOROUS MATERIALS;
CO OXIDATION;
HYDROGEN-PEROXIDE;
SELECTIVE OXIDATION;
CUO-CEO2;
CATALYSTS;
TERNARY HYDROTALCITES;
CU/CEO2;
LACTIC-ACID;
NANOPARTICLES;
CU;
D O I:
10.1039/c7ra00734e
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
We report on highly active CuO@ CeO2 catalysts prepared by the surfactant-template method and calcined at different temperatures. Then the obtained catalysts were characterized by means of various analytical techniques. Our findings show that the BET surface area and pore volume of the CuO@ CeO2 catalyst measured by N-2 adsorption-desorption are decreasing with the elevation of calcination temperature. From the results of XRD and XPS, we determined the oxidation state of copper in the copper-ceria mixed oxide catalysts. The CuO@ CeO2 (c)atalysts displayed good catalytic activity for the phenol hydroxylation using H2O2 as an oxidant. Moreover, we found that the catalytic activity is improved for high calcining temperature and the optimum conditions were obtained when the catalyst CuO@ CeO2 is calcined at 800 degrees C, which lead to higher phenol conversion of 54.62% with 92.87% of selectivity for catechol and hydroquinone. More importantly, the catalyst seems to be easily recovered by simple centrifugation. The results of catalyst recycling illustrated that the catalytic activity remained high even after five cycles with slight Cu leaching and slight loss of activity. Finally, a possible mechanism in phenol hydroxylation by H2O2 over CuO@ CeO2 catalyst was also proposed.
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页码:12586 / 12597
页数:12
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