60660-58-4Relevant articles and documents
Strong Metal Phosphide–Phosphate Support Interaction for Enhanced Non-Noble Metal Catalysis
Chen, Zemin,Zeng, Xiang,Li, Xinyu,Lv, Zhenxing,Li, Jiong,Zhang, Ying
, (2021/12/24)
Strong metal-support interaction (SMSI) is crucial for supported catalysts in heterogeneous catalysis. Here is the first report on strong metal phosphide-phosphate support interaction (SMPSI). The key to SMPSI is the activation of P species on the support, which leads to simultaneous generation of metal phosphide nanoparticles (NPs) and core–shell nanostructures formed by support migration onto the NPs. The encapsulation state of metal phosphide and charge transfer are identical to those of classical SMSIs and can be optimally regulated. Furthermore, the strong interactions of Co2PL/MnP-3 not only significantly enhance the anti-oxidation and anti-acid capability of non-noble metal but also exhibit excellent catalytic activity and stability toward hydrogenating a wide range of compounds into value-added fine chemicals with 100% selectivity, which is even better than Pd/C and Pt/C. The SMPSI construction can be generally extended to other systems such as Ni2PL/Mn3(PO4)2, Co2PL/LaPO4, and CoPL/CePO4. This study provides a new approach for the rational design of advanced non-noble metal catalysts and introduce a novel paradigm for the strong interaction between NPs and support.
Highly efficient catalytic conversion of cellulose into acetol over Ni-Sn supported on nanosilica and the mechanism study
Liu, Xiaohao,Liu, Xiaodong,Xu, Guangyue,Zhang, Ying,Wang, Chenguang,Lu, Qiang,Ma, Longlong
, p. 5647 - 5656 (2019/11/05)
Selective conversion of cellulose into high value-added C3 chemicals is a great challenge in biorefinery due to the complicated reaction process. In this work, 61.6% yield of acetol was obtained by one pot conversion of cellulose using Ni-Sn/SiO2 catalysts. A series of characterization methods including TEM, STEM-HAADF, EDS, AAS, XRD, XPS, H2-TPR, Py-FTIR, and CO2-TPD were carried out to explore the structure-activity relationship. The strong basicity of the catalysts was a key factor affecting the production of acetol. In addition, catalysts with the hydrothermally stable L-acid sites and no B-acid sites inhibited side reactions and ensured efficient conversion of cellulose into small molecules. Further studies showed that the formation of the Ni3Sn4 alloy significantly promoted the acetol production, and its weak hydrogenation activity inhibited further conversion of acetol. Noninteger valence tin species (Snδ+ and SnOx) were formed both in Ni3Sn4 and Sn/SiO2. These Sn species were the source of basic sites and the active sites for catalyzing cellulose to acetol. Under the synergistic catalysis of Sn/SiO2 and the Ni3Sn4 alloy, cellulose was efficiently converted into acetol. This work provides guidance for the selective conversion of cellulose into C3 products.
Hydrothermally Stable Ruthenium–Zirconium–Tungsten Catalyst for Cellulose Hydrogenolysis to Polyols
Lucas, Martin,Fabi?ovicová, Katarina,Claus, Peter
, p. 612 - 618 (2017/12/28)
In this work, we describe a catalytic material based on a zirconium–tungsten oxide with ruthenium for the hydrogenolysis of microcrystalline cellulose under hydrothermal conditions. With these catalysts, polyols can be produced with high yields. High and stable polyol yields were also achieved in recycling tests. A catalyst with 4.5 wt % ruthenium in total achieved a carbon efficiency of almost 100 %. The prepared Zr-W oxide is mesoporous and largely stable under hydrothermal conditions (493 K and 65 bar hydrogen). Decomposition into the components ZrO2 and WO3 could be observed at temperatures of 1050 K in air.
