Synthetic Strategies of Supported Pd-Based Bimetallic Catalysts for Selective Semi-Hydrogenation of Acetylene: A Review and Perspectives.

Selective semi-hydrogenation of acetylene is an extremely important reaction from both industrial and theoretical perspectives. Palladium, due to its unique chemical and physical properties, is the most active and currently irreplaceable metal for this reaction in industry, but the poor catalytic selectivity towards ethylene is also its inherent shortcoming. Introducing a secondary metal to tune a geometric and electronic structures of Pd nanoparticles and to create a synergistic effect is the most widely used strategy to effectively improve the overall catalytic performance of Pd-based catalysts. Thus, various supported Pd-based bimetallic catalysts for selective semi-hydrogenation of acetylene have been exploited in the past decade. Timely comparison, analysis, and summarizing of various preparation methods may offer a beneficial reference for the subsequent development of such catalysts. In this context, herein, the advances in synthesis strategies of catalysts, including nano-catalysts, single atom alloys (SAAs), as well as bimetallic dual atom catalysts are summarized systematically. Their advantages and disadvantages are comparatively discussed. Finally, future perspectives for the synthetic strategies of supported Pd-based bimetallic catalysts for selective semi-hydrogenation of acetylene are proposed.

Synthesis of Flower-Like Cobalt-Molybdenum Mixed-Oxide Microspheres for Deep Aerobic Oxidative Desulfurization of Fuel.

Flower-like cobalt-molybdenum mixed-oxide microspheres (CoMo-FMs) with hierarchical architecture were successfully synthesized via a hydrothermal process and subsequent calcination step. The characterization results show that CoMo-FMs were assembled from ultrathin mesoporous nanosheets with thicknesses of around 4.0 nm, providing the composite with a large pore volume and a massive surface area. The synthesized CoMo-FMs were employed as catalysts for the aerobic oxidative desulfurization (AODS) of fuel, and the reaction results show that the optimal catalyst (CoMo-FM-2) demonstrated an outstanding catalytic performance. Over CoMo-FM-2, various thiophenic sulfides could be effective removed at 80-110 °C under an atmospheric pressure, and a complete conversion of sulfides could be achieved in at least six consecutive cycles without a detectable change in chemical compositions. Further, the catalytic mechanism was explored by conducting systemic radical trapping and transformation experiments, and the excellent catalytic performance for CoMo-FMs should be mainly due to the synergistic effect of Mo and Co elements.

Design of Pd-Zn Bimetal MOF Nanosheets and MOF-Derived Pd3.9Zn6.1/CNS Catalyst for Selective Hydrogenation of Acetylene under Simulated Front-End Conditions.

Novel zinc-palladium-porphyrin bimetal metal-organic framework (MOF) nanosheets were directly synthesized by coordination chelation between Zn(II) and Pd(II) tetra(4-carboxyphenyl)porphin (TCPP(Pd)) using a solvothermal method. Furthermore, a serial of carbon nanosheets supported Pd-Zn intermetallics (Pd-Zn-ins/CNS) with different Pd: Zn atomic ratios were obtained by one-step carbonization under different temperature using the prepared Zn-TCPP(Pd) MOF nanosheets as precursor. In the carbonization process, Pd-Zn-ins went through the transformation from PdZn (650 °C) to Pd3.9Zn6.1 (~950 °C) then to Pd3.9Zn6.1/Pd (1000 °C) with the temperature increasing. The synthesized Pd-Zn-ins/CNS were further employed as catalysts for selective hydrogenation of acetylene. Pd3.9Zn6.1 showed the best catalytic performance compared with other Pd-Zn intermetallic forms.

2-Bromo-1,6,6-trimethyl-6,7,8,9-tetra-hydro-phenanthro[1,2-b]furan-10,11-dione.

In the title compound, C19H17BrO3, the ring skeleton is located on a crystallographic mirror plane; two C atoms of the cyclo-hexene ring are disordered over the two locations to satisfy the preferred ring conformation. In the crystal, C-H⋯O hydrogen bonds link the mol-ecules into chains along the a axis. π-π stacking inter-actions between benzo-quinone rings, with a centroid-centroid distance of 3.7225 (4) Å, are also observed, which connect the chains into a two-dimensional networkparallel to the ab plane.

Ni -chitosan/carbon nanotube: An efficient biopolymer -inorganic catalyst for selective hydrogenation of acetylene.

This work developed an efficient Ni catalyst based on chitosan for selective hydrogenation of acetylene. The Ni catalyst was prepared by the reaction of the chitosan/carbon nanotube composite with NiSO4 solution. The synthesized Ni-chitosan/carbon nanotube catalyst was characterized by inductively coupled plasma, FTIR, SEM and XRD. The results of FTIR and XRD demonstrated that Ni2+ successfully coordinated with chitosan. The addition of chitosan greatly improved the catalytic performances of Ni-chitosan/carbon nanotube catalyst. Over the Ni-chitosan/carbon nanotube catalyst, both the acetylene conversion and the selectivity to ethylene all achieved 100% at 160 °C and 190 °C, respectively. The catalytic performances of 6 mg Ni-chitosan/carbon nanotube catalyst were even better than that of 400 mg Ni single atom catalyst in literature. Extending the crosslinking time of chitosan and increasing the amount of the crosslinking agent were beneficial to enhance the catalytic effect of Ni-chitosan/carbon nanotube catalyst.