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Pd(II)-Fe(III)液相催化氧化净化磷化氢的研究

Pd(Ⅱ) –Fe(III) Catalyzed Oxidation of Phosphine in Aqueous Solution

中文摘要英文摘要

利用自主筛选的Pd(II)-Fe(III)二元催化体系净化磷化氢,提出催化氧化机理,进行了Pd2+和Fe3+离子浓度、温度、氧含量、磷化氢浓度、气体流速等对Pd(II)-Fe(III)催化体系净化含磷化氢尾气的影响研究。实验结果表明Pd(II)-Fe(III)二元催化体系在低温(22~73℃)、常压条件下存在着协同催化作用,对磷化氢的脱磷效率可在150min内保持100%。并且随氧含量增大、Pd(II)和 Fe(III)浓度增大催化剂稳定性增强。提出的催化氧化机理能合理的解释催化氧化净化过程中的动力学规律,进一步证明了Pd(II)-Fe(III)催化氧化磷化氢是双氧化还原机理。

Using independently screened Pd(II)-Fe(III) as catalyst for aqueous catalytic oxidation of phosphine and putting forward the catalysis mechanism , the effect of factors such as Pd2+ concentration, Fe2+ concentration, temperature, the velocity of inflow, oxygen concentration and phosphine concentration on phosphine purification efficiency was investigated. The results showed that at lower temperature(22-73℃) and under normal pressure, there existed synergistic effect between Pd(II) and Fe(III) and the purification efficiency of phosphine could keep 100% for more then 150min. In addition, when the oxygen concentration in inflow or Pd(II)-Fe(III) concentration in solution increased, catalysis activity of the catalyst would become more steady. It was also showed that the presumed mechanism could reasonably explain the kinetics characteristics and testified the catalytic oxidation depended on double-oxidation and double-reduction process.

宁平、李军燕、瞿广飞

金属元素无机化合物化学工业精细化学工业有机化学工业

催化氧化过渡金属离子磷化氢净化

catalytic oxidationtransition metallic ionphosphinepurification

宁平,李军燕,瞿广飞.Pd(II)-Fe(III)液相催化氧化净化磷化氢的研究[EB/OL].(2008-12-09)[2025-08-16].http://www.paper.edu.cn/releasepaper/content/200812-263.点此复制

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