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Surface chemistry related with VAM synthesis on palladium and gold-palladium model catalysts.

机译:在钯和金-钯模型催化剂上与VAM合成有关的表面化学。

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摘要

The acetoxylation of ethylene using palladium-based catalyst is a commercial route for the synthesis of vinyl acetate monomer (VAM) by the following reaction, even though some controversy existed about the mechanism by which this reaction occurs. C2H4+CH3COOH+1/2 O2→C2H3OOCCH3 +H2O The addition of gold into the catalyst improves its activity and selectivity, but the role of Au has not been elucidated. Thus, a full understanding of the role of Au on the catalyst surface is essential to further improve its performance.;The gold-palladium surface alloy model catalysts on Pd(111) and Pd(100) were prepared. The AuPd alloys on Pd(111) and Pd(100) were titrated with CO. CO adsorption was dominated by the geometric effects. CO oxidation was also studied on the alloy surface, and the atomic oxygen was found to be the active species for CO oxidation.;The adsorption properties of ethylene, acetic acid and VAM were strongly affected by the presence of gold on the surface. At high gold coverages, the ethylene adopts a pi-bonded configuration and then transforms to the di-sigma bonded configuration at the gold coverage below 0.5 ML. The acetic acid forms eta 1 species and then forms eta2 species when the gold coverage is below 0.4 ML. The presence of oxygen stabilizes the eta 2 species to 410 K before it decomposes. Vinyl acetate on clean Pd surface adsorbs with vinyl group in a pi-bonded configuration; however, the presence of high coverage gold causes the VAM to adopt a di-sigma bonding configuration. The oxygen was found to have the same effect as gold on VAM adsorption. At low gold coverages (below thetaAu ∼80%), the VAM molecule will completely decompose on Au/Pd(100), while it is stabilized on Au/Pd(111).;Overall, the alloy formed on Pd(111) increases the VAM selectivity due to the stability of VAM on the surface; the alloy formed on Pd(100) surface shows high activity, the selectivity is low due to the complete decomposition of VAM when the thetaAu is below ∼80%, This also confirms the enhanced VAM selectivity for high gold coverage on Au(100).
机译:使用钯基催化剂对乙烯进行乙氧基化是通过以下反应合成乙酸乙烯酯单体(VAM)的商业途径,即使该反应的发生机理存在一些争议。 C2H4 + CH3COOH + 1 / 2O2→C2H3OOCCH3 + H2O向催化剂中添加金可提高其活性和选择性,但尚未阐明Au的作用。因此,充分了解Au在催化剂表面的作用对于进一步提高其性能至关重要。制备了Pd(111)和Pd(100)上的金-钯表面合金模型催化剂。用CO滴定Pd(111)和Pd(100)上的AuPd合金。几何形状决定了CO的吸附。还对合金表面进行了CO氧化研究,发现原子氧是CO氧化的活性物种。;表面上金的存在强烈影响乙烯,乙酸和VAM的吸附性能。在高金覆盖率下,乙烯采用pi键结合构型,然后在低于0.5 ML的金覆盖率下转变为di-sigma键构型。当金的覆盖率低于0.4 ML时,乙酸形成eta 1物种,然后形成eta2物种。氧的存在在分解之前将eta 2物种稳定在410K。干净的Pd表面上的乙酸乙烯酯以pi键结构吸附乙烯基。但是,高覆盖率金的存在会导致VAM采用di-sigma键合配置。发现氧气对金的VAM吸附具有与金相同的作用。在低金覆盖率(低于thetaAu〜80%)下,VAM分子将在Au / Pd(100)上完全分解,而在Au / Pd(111)上稳定;总的来说,在Pd(111)上形成的合金会增加由于表面上VAM的稳定性,VAM选择性高; Pd(100)表面形成的合金表现出高活性,当thetaAu低于〜80%时,由于VAM的完全分解,选择性低,这也证实了Au(100)上高金覆盖率的VAM选择性提高。

著录项

  • 作者

    Li, Zhenjun.;

  • 作者单位

    The University of Wisconsin - Milwaukee.;

  • 授予单位 The University of Wisconsin - Milwaukee.;
  • 学科 Chemistry Physical.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 282 p.
  • 总页数 282
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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