The role of nanoporous carbon materials in catalytic cyclohexane oxidation

被引:28
作者
Andrade, Marta A. [1 ]
Mestre, Ana S. [2 ,3 ]
Carvalho, Ana P. [2 ,3 ]
Pombeiro, Armando J. L. [1 ]
Martins, Luisa M. D. R. S. [1 ]
机构
[1] Univ Lisbon, Ctr Quim Estrutural, IST, P-1049001 Lisbon, Portugal
[2] Univ Lisbon, Fac Ciencias, Ctr Quim & Bioquim, P-1749016 Lisbon, Portugal
[3] Univ Lisbon, Fac Ciencias, Ctr Quim Estrutural, P-1749016 Lisbon, Portugal
关键词
Immobilized catalyst; Oxidation; Cyclohexane; Iron scorpionate; Carbon materials; Activated carbon; ACTIVATED CARBONS; PEROXIDATIVE OXIDATION; SURFACE-CHEMISTRY; II COMPLEX; ADSORPTION; IRON; IRRADIATION; IBUPROFEN; REMOVAL; ALKANES;
D O I
10.1016/j.cattod.2019.07.036
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The C-scorpionate iron(II) complex [FeCl2(Tpm)] [Tpm = kappa(3)-HC(C3H3N2)(3)] was immobilized on three nanoporous carbon supports to produce active, selective and recyclable catalysts for the oxidation of cyclohexane. The influence of the porous carbon supports on the performance of the heterogenized [FeCl2(Tpm)] catalyst was investigated using materials with distinct porosity: microporous (GL50-ox, wet oxidized GL50 Norit sample, and S, sisal-derived activated carbon prepared by chemical activation), and mesoporous (CMK-3) materials. The heterogenized systems exhibited good activity and rather high selectivity to the formation of KA (ketone-alcohol) oil (cyclohexanol and cyclohexanone mixture) from microwave-assisted oxidation of cyclohexane, and allowed their easy recovery and reuse, at least for four consecutive cycles. The most important outcome of this work was the significant self-catalytic activity observed for the pristine carbon materials GL50-ox and CMK-3 towards cyclohexane oxidation under Microwave irradiation, in the absence of the iron complex.
引用
收藏
页码:46 / 55
页数:10
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