scholarly journals Preparation and Oxygen Permeability of BaCo0.7Fe0.2Nb0.1O3-δMembrane Modified by Ce0.8Y0.2O2-δPorous Layer on the Air Side

2013 ◽  
Vol 2013 ◽  
pp. 1-6
Author(s):  
Yuan Qiang ◽  
Zhen Qiang ◽  
Li Rong

BaCo0.7Fe0.2Nb0.1O3−δ(BCFN) dense ceramic membrane with submicron-Ce0.8Y0.2O2−δ(YDC) porous layer was investigated by the partial oxidation of coke oven gas (COG) in hydrogen production. XRD analysis showed this composite had good stability and no chemical reaction at high temperature. SEM and TEM characterization further showed BCFN membrane was uniformly modified by YDC porous layer (about 5~6 μm thickness) formed by the accumulation of relative nanoparticles. At the respective COG flux and air flux of 108 mL/min and 173 mL/min, the oxygen permeation flux of BCFN modified by submicron-YDC porous layer reached 16.62 mL·min−1·cm−2, which was about 23.5% higher than that of pure BCFN membrane. Therefore, submicron-YDC porous layer obviously improved the oxygen permeation flux of BCFN membrane and its stability at 875°C.

2010 ◽  
Vol 154-155 ◽  
pp. 877-881 ◽  
Author(s):  
Hong Wei Cheng ◽  
Xiong Gang Lu ◽  
Da Hai Hu ◽  
Yu Wen Zhang ◽  
Wei Zhong Ding ◽  
...  

The BaCo0.7Fe0.2Nb0.1O3-δ (BCFNO) membranes combined with Ce0.8Re0.2O2-δ (Re=La, Y) layer on the permeation side were used for hydrogen production by partial oxidation reforming of coke oven gas (COG). The Ce0.8Re0.2O2-δ improved the oxygen permeation flux of the membrane by 11–28% at 750 oC. The high oxygen permeation flux achieved using the Ce0.8Re0.2O2-δ surface-coating layer in this work are quite encouraging with a maximum value reaching 19.7 ml/cm2•min at 900 oC, which will be promising surface modification materials in the catalytic partial oxidation reforming of COG.


2010 ◽  
Vol 156-157 ◽  
pp. 1024-1028
Author(s):  
Da Hai Hu ◽  
Xiong Gang Lu ◽  
Hong Wei Cheng ◽  
Wei Zhong Ding

The performance of Ni/SiO2 Catalysts modified by La2O3, ZrO2 and CeO2 were tested in a BaCo0.7Fe0.2Nb0.1O3-δ (BCFNO) membrane reactor by catalytic partial oxidation of coke oven gas (COG) under atmospheric pressure. The results show that the oxygen permeation flux increased dramatically with Ni/RxOy/SiO2 (R = La, Zr or Ce) catalysts by adding the element of rare earth especially the La during the reforming reaction. At optimized reaction conditions, the dense oxygen permeable membrane had an oxygen permeation flux around 16.4 ml/cm2•min and a CH4 conversion of 99.2% have been achieved at 900 oC.


2014 ◽  
Vol 628 ◽  
pp. 319-322
Author(s):  
Zhi Bin Yang

In this paper we found two catalysts exhibit high catalytic activity and stability during the partial oxidation of methane (POM) in Coke oven gas (COG) in BCFNO membrane reactor. Such as the NiO/MgO catalyst, we discussed the COG and air flow rate on the performance of reforming of COG. The results show that the NiO/MgO catalyst exhibits high activity. The experimental result of the CH4 conversion, selectivity of H2 and CO were suited well to the result of thermodynamic analysis. And the LiNiCeO/γ-Al2O3 catalyst, we discussed the LiNiCeO/γ-Al2O3 catalysts with different amount CeO2 in order to compare the reaction performance on the membrane reactor. The results show that the oxygen permeation flux increased significantly with increasing the amount of CeO2 during the POM in COG. Such as, the LiNi15%CeO/γ-Al2O3 catalyst with a oxygen permeation flux of 10.6 ml⋅cm-2⋅min-1 and a 100% CH4 conversion were obtained at 875 oC.


2012 ◽  
Vol 560-561 ◽  
pp. 959-964 ◽  
Author(s):  
Jong Pyo Kim ◽  
Dae Woong Pyo ◽  
Edoardo Magnone ◽  
Jung Hoon Park

ReBaCo2O5+δ (Re=Pr, Nd, Y) oxides were synthesized by solid state reaction method. The oxygen permeation flux of ReBaCo2O5+δ (Re=Pr, Nd, Y) membranes increased with temperature and oxygen partial pressure and ranked as follow: PrBaCo2O5+δ > NdBaCo2O5+δ > YBaCo2O5+δ. The oxygen permeation response of PrBaCo2O5+δ membrane was fairly stable and no detectable degradation is observed at high temperature under carbon dioxide conditions (CO2 = 500 ppm).


2011 ◽  
Vol 377 (1-2) ◽  
pp. 198-205 ◽  
Author(s):  
S. Baumann ◽  
J.M. Serra ◽  
M.P. Lobera ◽  
S. Escolástico ◽  
F. Schulze-Küppers ◽  
...  

Ceramics ◽  
2019 ◽  
Vol 2 (2) ◽  
pp. 246-259 ◽  
Author(s):  
Cyril Gaudillere ◽  
Julio Garcia-Fayos ◽  
Jorge Plaza ◽  
José M. Serra

An original asymmetric tubular membrane for oxygen production applications was manufactured in a two-step process. A 3 mol% Y2O3 stabilized ZrO2 (3YSZ) porous tubular support was manufactured by the freeze-casting technique, offering a hierarchical and radial-oriented porosity of about 15 µm in width, separated by fully densified walls of about 2 µm thick, suggesting low pressure drop and boosted gas transport. The external surface of the support was successively dip-coated to get a Ce0.8Gd0.2O2−δ – 5mol%Co (CGO-Co) interlayer of 80 µm in thickness and an outer dense layer of La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF) with a thickness of 30 µm. The whole tubular membrane presents both uniform geometric characteristics and microstructure all along its length. Chemical reactivity between each layer was studied by coupling X-Ray Diffraction (XRD) analysis and Energy Dispersive X-Ray spectroscopy (EDX) mapping at each step of the manufacturing process. Cation interdiffusion between different phases was discarded, confirming the compatibility of this tri-layer asymmetric ceramic membrane for oxygen production purposes. For the first time, a freeze-cast tubular membrane has been evaluated for oxygen permeation, exhibiting a value of 0.31 ml·min−1·cm−2 at 1000ºC under air and argon as feed and sweep gases, respectively. Finally, under the same conditions and increasing the oxygen partial pressure to get pure oxygen as feed, the oxygen permeation reached 1.07 ml·min−1·cm−2.


AIChE Journal ◽  
2010 ◽  
Vol 56 (12) ◽  
pp. 3084-3090 ◽  
Author(s):  
Barbara Zydorczak ◽  
Kang Li ◽  
Xiaoyao Tan

2005 ◽  
Vol 885 ◽  
Author(s):  
Hitoshi Takamura ◽  
Masayuki Ogawa ◽  
Yusuke Aizumi ◽  
Atsunori Kamegawa ◽  
Masuo Okada

ABSTRACTThis paper describes preparation and methane reforming characteristics of a proto-type reformer based on a composite-type oxygen permeable membrane. The tape-cast membrane of Sm-doped CeO2 and 15 vol% MnFe2O4 composite was combined with ferric stainless steel separator with a same thermal expansion coefficient. For the reformer module, high CH4 conversion, CO and H2 selectivity of 96%, 84% and 89% were achieved, respectively. Based on C, H and O balances, oxygen permeation flux was found to be 5.7 mu-mol/cm2s. Joule heat caused by the oxygen permeation was estimated to be approximately 17.5 W, and this covered most part of heat required for reforming reactions.


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