【摘 要】
:
Double-perovskite type oxide LaSrFeCoO6(LSFCO) was used as oxygen carrier for chemical looping steam methane reforming (CL-SMR) due to its unique structure and reactivity.Two different oxidation routes,steam-oxidation and steam-air-stepwise-oxidation,were
【机 构】
:
Guangdong Key Laboratory of New and Renewable Energy Research and Development, Guangzhou Institute o
论文部分内容阅读
Double-perovskite type oxide LaSrFeCoO6(LSFCO) was used as oxygen carrier for chemical looping steam methane reforming (CL-SMR) due to its unique structure and reactivity.Two different oxidation routes,steam-oxidation and steam-air-stepwise-oxidation,were applied to investigate the recovery behaviors of the lattice oxygen in the oxygen carrier.The characterizations of the oxide were determined by X-ray diffraction (XRD),X-ray photoelectron spectroscopy (XPS),hydrogen temperature-programmed reduction (H2-TPR) and scanning electron microscopy (SEM).The fresh sample LSFCO exhibits a monocrystalline perovskite structure with cubic symmetry and high crystallinity,except for a little impurity phase due to the antisite defect of Fe/Co disorder.The deconvolution distribution of XPS patterns indicated that Co,and Fe are predominantly in an oxidized state (Fe3+ and Fe2+) and (Co2+ and Co3+),while O 1s exists at three species of lattice oxygen,chemisorbed oxygen and physical adsorbed oxygen.The double perovskite structure and chemical composition recover to the original state after the steam and air oxidation,while the Co ion cannot incorporate into the double perovskite structure and thus form the CoO just via individual steam oxidation.In comparison to the two different oxidation routes,the sample obtained by steam-oxidation exhibits even higher CH4 conversion,CO and H2 selectivity and stronger hydrogen generation capacity.
其他文献
An approach to the simultaneous reclamation of carbon and sulfur resources from C02 and H2S has been proposed and effectively implemented with the aid of catalysts.A brief thermodynamic study reveals the potential of direct reduction of C02 with H2S (15:1
Porous nanocarbons with average particle size 20-40 nm were developed using biowaste oil palm leaves as a precursor.Simple pyrolysis was carried out at 700 ℃ under nitrogen atmosphere.Obtained porous nanocarbons showed excellent porous nature along with s
LiNi0.915Co0.075Al0.01O2 (NCA) with Zr(OH)4 coating is demonstrated as high performance cathode material for lithium ion batteries (LIBs).The coated materials are synthesized via a simple dry coating method of NCA with Zr(OH)4 powders,and then characteriz
A series of novel carbon nanofibers (CNFs) based Cu-ZrO2 catalysts were synthesized by deposition precipitation method.To investigate the influence of promoter,catalysts were loaded with 1,2,3 and 4 wt% ZnO and characterized by ICP-OES,HRTEM,BET,N2O chemi
The highly ordered TiO2 nanotubes (NTs) were fabricated by the anodic oxidation method.Their morphology,structure and crystalline phase were characterized by scanning electron microscopy (SEM) and X-ray diffractometer (XRD).The effects of morphology,speci
A series of self-reducing bifunctional Ni-W/SBA-15 catalysts were synthesized using biomass-based carbon source as the reducing agent without conventional further reduction step.The self-reducing catalysts were performed on the hydrogenolysis of cellulose
A composite interlayer comprised of gadolinia doped ceria (GDC) and Co/Fe oxide was prepared and investigated for solid oxide electrolysis cell with yttrium stabilized zirconia (YSZ) electrolyte and La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF) anode.The interlayer was
In terms of the reaction of CO2 reduction to CO with hydrogen,CO2 conversion is very low at low temperature due to the limitation of thermodynamic equilibrium (TE).To overcome this limitation,plasma catalytic reduction of CO2 to CO in a catalyst-filled di
Lithium-sulfur batteries have great potential for high energy applications due to their high capacities,low cost and eco-friendliness.However,the particularly rapid capacity decay owing to the dissolution and diffusion of polysulfide intermediate into the