Exploration of the preparation of Cu/TiO2 catalysts by deposition–precipitation with urea for selective hydrogenation of unsaturated hydrocarbons

催化作用 化学 奥斯特瓦尔德成熟 吸附 降水 成核 金属 纳米颗粒 无机化学 尿素 沉积(地质) 化学工程 物理化学 有机化学 古生物学 物理 沉积物 气象学 工程类 生物
作者
Zhao Wang,Dalil Brouri,Sandra Casale,Laurent Delannoy,Catherine Louis
出处
期刊:Journal of Catalysis [Elsevier BV]
卷期号:340: 95-106 被引量:55
标识
DOI:10.1016/j.jcat.2016.05.011
摘要

Deposition–precipitation with urea (DPu) was used to deposit copper on TiO2 and prepare metal Cu/TiO2 catalysts with different Cu loadings from 0.6 to 4.2 wt%. Cu2+ complexes adsorb on TiO2 at pH lower than PZCTiO2 (around 6), i.e., when the titania surface is supposed to be positively charged. To attempt to explain these results, a study on the deposition behavior of Cu2+ was carried out as a function of the pH of the preparation solution and the Cu loading. The samples were characterized by XRD, UV–visible, TPR and electron microscopy leading to a chemical mechanism of copper deposition: the presence of some negatively charged Ti–O sites on the TiO2 surface even at low pH could be responsible for the Cu2+ complex adsorption, but it has not been possible to discard the occurrence of a surface reaction with OHs of titania. In fine, these adsorbed Cu2+ species formed Ti–O–Cu bonding, and were proposed to act as nucleation sites for the formation of Cu2(OH)3NO3 particles onto the support. As DPu proceeded, these particles grew according to Ostwald ripening mechanism, and became unstable and transformed into CuO depending on the final Cu loading and DPu duration. As a result, the size of Cu0 nanoparticles obtained after reduction at 350 °C strongly depends on the Cu loading and the DPu time: very small Cu0 particles (<1 nm) in the low loaded samples (<1 wt% Cu) resulting from the presence of small particles of Cu2(OH)3NO3 after preparation, moderate Cu0 particle size (∼3 nm) in samples initially containing larger particles of Cu2(OH)3NO3 and additional large particles (>10 nm) in samples containing CuO. The Cu catalysts exhibit interesting potential for selective hydrogenation of butadiene at relatively low temperature with good activity and high selectivity. The highest activity and stability were obtained with the samples containing small metal Cu particles, i.e., the samples exempt of CuO after preparation.
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