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Direct Synthesis of Hydrogen Peroxide from Hydrogen and Oxygen over Pd-supported Metal-Organic Framework Catalysts

机译:钯载金属有机骨架催化剂上的氢氧直接合成过氧化氢

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摘要

Pd-supported metal-organic framework (MOF) catalysts have been applied for the direct synthesis of H2O2 from H-2 and O-2 under intrinsically safe and noncorrosive reaction conditions. The catalytic performance was strongly governed by the properties of the support materials, and the BrOnsted acid sites newly introduced on the organic linkers of MOF were proven to be more effective than the Lewis acid sites on the open metal sites in enhancing the H2O2 formation and suppressing its decomposition. Pd/MIL-101-SO3H was highly efficient in promoting the reaction owing to the contribution from the strong acidity and highly porous nature of the robust MOF support used. The hydrogen peroxide productivity of Pd/MIL-101-SO3H catalyst reached 361mmol H2O2 mmol/Pd/h, which was 2.3 or 1.7 times higher than that of the conventional Pd/HBEA (SAR=25) or Pd/sulfonated resin catalyst, respectively. This result clearly demonstrates the promising potential of MOF as a solid acid support material.
机译:Pd负载的金属有机骨架(MOF)催化剂已被用于在本质安全且无腐蚀的反应条件下由H-2和O-2直接合成H2O2。催化性能受载体材料性能的强烈支配,事实证明,MOF有机连接基上新引入的布朗斯台德酸部位比开放金属部位的路易斯酸部位在增强H2O2形成和抑制方面更有效。它的分解。 Pd / MIL-101-SO3H由于使用的坚固的MOF载体具有强酸性和高度多孔性,因此在促进反应方面非常有效。 Pd / MIL-101-SO3H催化剂的过氧化氢生产率达到361mmol H2O2 mmol / Pd / h,分别是常规Pd / HBEA(SAR = 25)或Pd /磺化树脂催化剂的2.3或1.7倍。该结果清楚地证明了MOF作为固体酸载体材料的潜力。

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