Su Penghe, Liu Xiaotong, Chen Ya, Liu Hongchi, Zhu Baolin, Zhang Shoumin, Huang Weiping
College of Chemistry, Nankai University, Tianjin 300071, China.
The Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China.
Nanomaterials (Basel). 2018 Sep 25;8(10):755. doi: 10.3390/nano8100755.
The TiO₂-based nanotubes (TNTs, B⁻TNTs) of different surface acidities and their supported Rh catalysts were designed and synthesized. The catalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectrometer (XPS), tempera⁻ture⁻programmed desorption of ammonia (NH₃⁻TPD), atomic emission spectrometer (ICP), and Brunauer⁻Emmett⁻Tellerv (BET) surface-area analyzers. Images of SEM and TEM showed that the boron-decorated TiO₂ nanotubes (B⁻TNTs) had a perfect multiwalled tubular structure; their length was up to hundreds of nanometers and inner diameter was about 7 nm. The results of NH₃-TPD analyses showed that B⁻TNTs had a stronger acid site compared with TNTs. For Rh/TNTs and Rh/B⁻TNTs, Rh nanoparticles highly dispersed on B⁻TNTs were about 2.79 nm in average diameter and much smaller than those on TNTs, which were about 4.94 nm. The catalytic performances of catalysts for the hydroformylation of 2-methyl-3-butennitrile (2M3BN) were also evaluated, and results showed that the existence of B in Rh/B⁻TNTs had a great influence on the catalytic performance of the catalysts. The Rh/B⁻TNTs displayed higher catalytic activity, selectivity for aldehydes, and stability than the Rh/TNTs.
设计并合成了具有不同表面酸度的二氧化钛基纳米管(TNTs,B⁻TNTs)及其负载的Rh催化剂。采用X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、X射线光电子能谱仪(XPS)、氨程序升温脱附(NH₃⁻TPD)、原子发射光谱仪(ICP)和布鲁瑙尔-埃米特-特勒尔(BET)比表面积分析仪对催化剂进行了表征。SEM和TEM图像表明,硼修饰的二氧化钛纳米管(B⁻TNTs)具有完美的多壁管状结构;其长度可达数百纳米,内径约为7nm。NH₃-TPD分析结果表明,与TNTs相比,B⁻TNTs具有更强的酸性位点。对于Rh/TNTs和Rh/B⁻TNTs,高度分散在B⁻TNTs上的Rh纳米颗粒平均直径约为2.79nm,比TNTs上的(约4.94nm)小得多。还评估了催化剂对2-甲基-3-丁烯腈(2M3BN)氢甲酰化反应的催化性能,结果表明Rh/B⁻TNTs中B的存在对催化剂的催化性能有很大影响。Rh/B⁻TNTs比Rh/TNTs表现出更高的催化活性、对醛的选择性和稳定性。