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    无掺杂g-C3N4促进光催化甲苯氧化

    Undoped g-C3N4 boosted photocatalytic oxidation of toluene

    • 摘要: 以O2选择性氧化甲苯转化为高附加值氧化物意义重大且具有挑战。为解决甲苯C(sp3)-H难以活化问题, 成功将无掺杂的g-C3N4应用于甲苯氧化反应, 展现出优异的光催化氧化活性。经二次热剥离处理的g-C3N4, 比表面积显著增大, 可以提供更多的活性位点, 同时促进了光生电子-空穴的有效分离与迁移, 大的比表面积也有利于对甲苯和O2的吸附。经优化后的光催化剂在400~410 nm光照条件下, 以O2为氧化剂, 室温条件反应8 h, 甲苯转化率为65.8%, 苯甲醛和苯甲酸总选择性为86.2%, 甲苯转化速率可达2 056 μmol·(g·h)-1

       

      Abstract: Selective oxidation of toluene into high value-added oxides is significant and challenging with O2.An undoped g-C3N4 was prepared by a simple thermal exfoliation method to solve the difficulty of toluene C(sp3)-H activation, which showed excellent photocatalytic activity.The specific surface area of g-C3N4 was significantly increased after secondary thermal exfoliation treatment, which provides more active sites and promotes the effective separation and migration of photogenerated electron-holes.The large specific surface area is conducive to the adsorption of toluene and O2.The optimized photocatalyst displays 86.2%total selectivity of benzaldehyde and benzoic acid, with 65.8%conversion under 400~410 nm light irradiation for 8 h at room temperature using O2 as oxidant, while the toluene conversion rate is 2 056μmol·(g·h)-1.

       

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