催化作用
化学
无机化学
齿合度
钼酸盐
水溶液
钼
高氯酸盐
金属
离子
有机化学
作者
Changxu Ren,Peng Yang,Jiaonan Sun,Eric Bi,Jacob Palmer,Mengqiang Zhu,Yiying Wu,Jinyong Liu
标识
DOI:10.26434/chemrxiv.13107743.v1
摘要
The detection of perchlorate (ClO 4 − ) on and beyond Earth requires ClO 4 − reduction technologies to support water purification and space exploration. However, the reduction of ClO 4 − usually entails either harsh conditions or multi-component enzymatic processes. We developed a heterogeneous Mo−Pd/C catalyst from sodium molybdate to reduce aqueous ClO 4 − into Cl − with 1 atm H 2 at room temperature. Upon hydrogenation by H 2 /Pd, the reduced Mo oxide species and a bidentate nitrogen ligand (1:1 molar ratio) are transformed in situ into oligomeric Mo sites on the carbon support. The turnover number and frequency for oxygen atom transfer from ClO x − substrates reached 3850 and 165 h −1 on each Mo site. This simple bioinspired design yielded a robust water-compatible catalyst for the removal and utilization of ClO 4 − .
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