Nd-Doped Barium Cerate Nano-Sized Catalyst Converts CH4 into CO2 at Lower Temperature Compared to Noble Metal-Based Pd/Al2O3 Catalyst

The present paper describes the synthesis and first application of Nd-doped BaCeO3 nanoparticles as catalyst for the catalytic oxidation of methane (CH4) into CO2. Nd-doped barium cerate BaCeO3 nanoparticles, with the formula BaNdxCe(1-x)O3, have been prepared using a simple sol gel method starting from acetate precursors. The as-prepared nanoparticles have been fully characterized by XRD, TEM, HRTEM and specific surface area measurement. Results confirmed the formation of highly crystallized nano-sized particles with small crystallite size. In-situ FTIR spectroscopy was used to study the catalytic conversion of methane (CH4) into CO2 in the presence of the as-prepared Nd-doped BaCeO3 nanocatalyst. The catalytic properties of such nanocatalysts have been discussed and correlated to Nd-doping rate, crystallite diameter, and specific surface area of the materials. Excellent catalytic properties have been obtained with BaNd0.05Ce0.95O3, such as, superior conversion efficiency, longer catalysis lifetime and lower activation temperature compared to un-doped BaCeO3 catalyst. Interestingly, it was found that BaNd0.05Ce0.95O3 nanocatalyst successfully converts the totality of CH4 present in a mixture of CH4-Air into CO2 at much lower temperature compared to the conventional Pd/Al2O3 catalyst.

Comparative thermal research on tetraazapentalene-derived heat-resistant energetic structures

Organic inner salt structures are ideal backbones for heat-resistant energetic materials and systematic studies towards the thermal properties of energetic organic inner salt structures are crucial to their applications. Herein, we report a comparative thermal research of two energetic organic inner salts with different tetraazapentalene backbones. Detailed thermal decomposition behaviors and kinetics were investigated through differential scanning calorimetry and thermogravimetric analysis (DSC-TG) methods, showing that the thermal stability of the inner salts is higher than most of the traditional heat-resistant energetic materials. Further studies towards the thermal decomposition mechanism were carried out through condensed-phase thermolysis/Fourier-transform infrared (in-situ FTIR) spectroscopy and the combination of differential scanning calorimetry-thermogravimetry-mass spectrometry-Fourier-transform infrared spectroscopy (DSC-TG-MS-FTIR) techniques. The experiment and calculation results prove that the arrangement of the inner salt backbones has great influence on the thermal decompositions of the corresponding energetic materials. The weak N4-N5 bond in “y-” pattern tetraazapentalene backbone lead to early decomposition process and the “z-” pattern tetraazapentalene backbone exhibits more concentrated decomposition behaviors.

Adsorption Properties of Ce5(BDC)7.5(DMF)4 MOF

In this article we report on the spectroscopic and adsorptive studies done on Ce(III)-based MOF possessing, upon desolvation, open metal sites, and a discrete surface area. The Ce-based MOF was synthesized from terephthalic acid linker (H2BDC) and Ce3+ cations by the classical solvothermal method. Preliminary powder X-ray diffraction analysis showed that the obtained materials corresponded to the ones reported by other authors. Spectroscopic techniques, such as XAS and in situ FTIR with probe molecules were used. In situ FTIR spectroscopy confirmed the successful removal of DMF molecules within the pore system at temperatures above 250 °C. Moreover, the use of CO as a probe molecule evidenced the presence of a Ce3+ open metal sites. Detailed volumetric and calorimetric CO2 adsorption studies are also reported.