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Efficient removal and recovery of copper by liquid phase catalytic hydrogenation using highly active and stable carbon-coated Pt catalyst supported on carbon nanotube

机译:使用负载在碳纳米管上的高活性和稳定的碳包覆Pt催化剂通过液相催化氢化有效去除和回收铜

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摘要

In this work, we coated carbon nanotubes (CNT) supported Pt catalyst by conductive carbon layers (labelled as Pt/CNT@C) and the catalyst was further functionalized by surface oxidation (denoted as Pt/CNT@Oxi-C). The textural properties of the catalysts were extensively characterized and liquid phase catalytic hydrogenation reduction of Cu2+ was conducted. Results showed that Pt particles of Pt/CNT@C and Pt/CNT@Oxi-C were completely embedded beneath carbon overcoatings. Furthermore, contrary to Pt/CNT no CO chemisorption was observed on both Pt/CNT@C and Pt/CNT@Oxi-C, indicative of the absence of exposed Pt particles in carboncoated Pt/CNT. Effective Cu2+ reduction and metallic Cu deposition by catalytic hydrogenation were achieved on catalyst surface. Surface oxidation of Pt/CNT@C resulted in increased surface wetting and functionality content, leading to noticeable enhancement in catalytic activity for Cu2+ reduction. Additionally, Cu2+ reduction on Pt/CNT@Oxi-C proceeded through the Langmuir-Hinshelwood model, suggesting that the reduction of Cu2+ adsorbed on catalyst surface was the rate-determining step. Carbonization of overcoatings exhibited a volcano-type relationship between carbonization temperature and catalytic activity of Pt/CNT@C for Cu2+ reduction. As for catalyst reuse, Pt/CNT lost 92 % of initial activity after five consecutive reaction cycles, whereas Pt/CNT@Oxi-C maintained a high catalytic activity without remarkable deactivation.
机译:在这项工作中,我们通过导电碳层(标记为Pt / CNT @ C)涂覆了碳纳米管(CNT)负载的Pt催化剂,并且该催化剂通过表面氧化进一步功能化(表示为Pt / CNT @ Oxi-C)。广泛表征了催化剂的质构性质,并进行了液相催化加氢还原Cu2 +。结果表明,Pt / CNT @ C和Pt / CNT @ Oxi-C的Pt颗粒完全被碳覆盖层覆盖。此外,与Pt / CNT相反,在Pt / CNT @ C和Pt / CNT @ Oxi-C上均未观察到CO化学吸附,表明在碳涂层的Pt / CNT中不存在暴露的Pt颗粒。通过催化加氢在催化剂表面实现了有效的Cu 2+还原和金属Cu沉积。 Pt / CNT @ C的表面氧化导致表面润湿性和官能度含量增加,从而导致Cu2 +还原的催化活性显着增强。另外,通过Langmuir-Hinshelwood模型进行了Pt / CNT @ Oxi-C上Cu2 +的还原,这表明吸附在催化剂表面的Cu2 +的还原是决定速率的步骤。外涂层的碳化显示出碳化温度与Pt / CNT @ C催化Cu2 +还原活性之间的火山型关系。至于催化剂的再利用,Pt / CNT在连续五个反应循环后损失了92%的初始活性,而Pt / CNT @ Oxi-C则保持了较高的催化活性而没有明显的失活。

著录项

  • 来源
    《Journal of Hazardous Materials》 |2020年第15期|121745.1-121745.10|共10页
  • 作者

  • 作者单位

    Nanjing Univ State Expt Teaching Demonstrat Ctr Environm Sci & Sch Environm State Key Lab Pollut Control & Resource Reuse Nanjing 210023 Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Liquid phase catalytic hydrogenation; Cu2+; Carbon nanotube supported Pt; Coated catalysts;

    机译:液相催化加氢;Cu 2+;碳纳米管负载的铂涂层催化剂;

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