Effects of shot peening and laser remelting on oxygen-permeation treatment of titanium alloy

The influence of surface pre-treatments, shot-peening (SP) and laser remelting (LR), on oxygen permeation behaviors of titanium alloy TC11 was investigated. Optical microscope, SEM with EDAX, XRD, and microhardness tester were employed to characterize the microstructure, composition and hardness of this alloy. The results show that the surface roughness is increased by shot-peening, and the microstructure with fine-grain can be obtained by LR pre-treatment. The pre-treated samples were oxygen-permeated at (810± 10) ℃ for 10 h in atmospheric air. The outer layer consists essentially of TiO2, trace Ti2 N, Ti3Al and Ti3AlN for the SP pre-treatment and thin oxygen solution layer is found in the subsurface layer. As for LR pre-treatment, the outer layer consists mainly of TiO2 and small amounts of TiO, and the inner layer consists of alpha crystals, rich in interstitial atoms. Samples by LR pre-treatment has thicker hardened layer with higher hardness values in comparison with SP pre-treated ones.The boost diffusion of oxygen and hardening mechanisms were discussed based on the experimental results.

Perovskite-type oxygen-permeable membrane BaCo_(0.7)Fe_(0.2)Nb_(0.1)O_(3-δ) for partial oxidation of methane in coke oven gas to hydrogen

Perovskite-type oxygen-permeable membrane reactors of BaCo0.7Fe0.2Nb0.1O3-δ （BCFNO） packed with Ru-based catalyst had high oxygen permeability and could be used for hydrogen production by partial oxidation of methane in coke oven gas （COG）. At 1173 K, 94% of methane conversion, 85% of H2 selectivity, 107% of CO selectivity, and as high as 15.4 mL·cm^-2·min^-1 of oxygen permeation flux were obtained. The BCFNO membrane itself had poor catalytic activity to partial oxidation of CH4 in COG. During continuous operation for 70 h at 1173 K, no degradation of the membrane reaction performance was observed. XRD and SEM characterization also demonstrated that the BCFNO membrane reactor exhibited good stability in partial oxidation of methane in COG.

Performance of a tubular oxygen-permeable membrane reactor for partial oxidation of CH_4 in coke oven gas to syngas

A gas-tight BaCo 0.7 Fe 0.2 Nb 0.1 O 3-δ（BCFNO） tubular membrane was fabricated by hot pressure casting.And a membrane reactor with BCFNO tubular membrane and Ag-based sealant was readily constructed and applied to partial oxidation of CH4 in coke oven gas.At 875 ℃,95% of methane conversion,91% of H 2 and as high as 10 ml cm-2·min-1 of oxygen permeation flux were obtained.There was a good match in the coefficient of thermal expansion between Ag-based alloy and BCFNO membrane materials.The tubular BCFNO membrane reactor packed with Ni-based catalysts exhibited not only high activity but also good stability in hydrogen-enriched coke oven gas（COG） atmosphere.

Methane Aromatization Upgraded by Oxygen-Permeable Membrane Reactor

Recently the CAS Qingdao Institute of Bioenergy and Processes in collaboration with the Leibniz Universit?t Hannover,Forschungszentrum Jülich and Bayer AG has made attempts to carry out methane aromatization reaction in an oxygen-permeable membrane reactor to

Partial oxidation of simulated hot coke oven gas to syngas over Ru-Ni/Mg(Al)O catalyst in a ceramic membrane reactor

Hydrogen amplification from simulated hot coke oven gas （HCOG） was investigated in a BaCo0.7Fe0.2Nb0.1O3-δ （BCFNO） membrane reactor combined with a Ru-Ni/Mg（Al）O catalyst by the partial oxidation of hydrocarbon compounds under atmospheric pressure. Under optimized reaction conditions, the dense oxygen permeable membrane had an oxygen permeation flux around 13.3 ml/（cm^2·min）. By reforming of the toluene and methane, the amount of H2 in the reaction effluent gas was about 2 times more than that of original H2 in simulated HCOG. The Rn-Ni/Mg（Al）O catalyst used in the membrane reactor possessed good catalytic activity and resistance to coking. After the activity test, a small amount of whisker carbon was observed on the used catalyst, and most of them could be removed in the hydrogen-rich atmosphere, implying that the carbon deposition formed on the catalyst might be a reversible process.