Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userHigh CO2-tolerance oxygen permeation dual-phase membranes Ce0.9Pr0.1O2-{delta}-Pr0.6Sr0.4Fe0.8Al0.2O3-{delta}
490
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
High stability and oxygen permeability are two prominent requirements for the oxygen transport membrane candidates used as industrialization. Herein, we report several composite membranes based on xwt.%Ce0.9Pr0.1O2(CPO)-(100-x)wt.%Pr0.6Sr0.4Fe0.8Al0.2O3(PSFAO) (x = 50, 60 and 75) prepared via a modified Pechini method. Oxygen permeability test reveals that the 60CPO-40PSFAO composition exhibits the highest oxygen permeability. The oxygen permeation flux through the optimal uncoated 0.33 mm-thickness 60CPO-40PSFAO composite can reach 1.03 mL cm-2 min-1 (over the general requirement value of 1 mL cm-2 min-1) in air/He atmosphere at 1000 {deg}C. In situ XRD performance confirms the optimal 60CPO-40PSFAO sample shows excellent stability in CO2-containing atmospheres. The 60CPO-40PSFAO membrane still exhibits simultaneously excellent oxygen permeability and phase stability after operating for over 100 h at air/CO2 condition at 1000 {deg}C, which further indicates that the 60CPO-40PSFAO composite is likely to be used for oxygen supply in CO2 capture
rate research
Read More
A series of composites based on (100-x)wt.%Ce0.9Pr0.1O2-{delta}-xwt.%Pr0.6Ca0.4FeO3-{delta} (x = 25, 40 and 50) doped with the cheap and abundant alkaline earth metal Ca2+ at the A-site has been successfully designed and fabricated. The crystal structure, oxygen permeability, phase and CO2 stability were evaluated. The composition of 60wt.%Ce0.9Pr0.1O2-{delta}-40wt.%Pr0.6Ca0.4FeO3-{delta}(60CPO-40PCFO) possesses the highest oxygen permeability among three studied composites. At 1000 oC, the oxygen permeation fluxes through the 0.3 mm-thickness 60CPO-40PCFO membranes after porous La0.6Sr0.4CoO3-{delta} each to 1.00 mL cm-2 min-1 and 0.62 mL cm-2 min-1 under air/He and air/CO2 gradients, respectively. In situ XRD results demonstrated that the 60CPO-40PCFO sample displayed a perfect structural stability in air as well as CO2-containing atmosphere. Thus, low-cost, Co-free and Sr-free 60CPO-40PCFO has high CO2 stability and is economical and environmental friendly since the expensive and volatile element Co was replaced by Fe and Sr was waived since it easily forms carbonates.
Ceramic dual-phase oxygen transport membranes with the composition of 60wt.% Ce0.9Pr0.1O2-{delta}-40wt.%Pr0.6Sr0.4Fe1-xAlxO3-{delta} (x = 0.05, 0.1, 0.2, 0.3, 0.4, 0.6, 0.8, 1.0) (60CPO-40PSF1-xAxO) based on 60Ce0.9Pr0.1O2-{delta}-40Pr0.6Sr0.4FeO3-{delta} doped Al was successfully synthesized through a modified Pechini method. Crystal structure, surface microtopography and oxygen permeability are investigated systematically. The cell parameters of perovskite phase first increased and then decreased with the increase of Al content, which is related to the radius of the Al3+ and the formation of impurity phase. As x ranges from 0.1 to 0.8, the oxygen permeability of the materials first increases and then decreases, and the maximum value of oxygen permeation rate for 60CPO-40PSF1-xAxO membranes with 0.4mm thickness at 1000 {deg}C is 1.12 mL min-1 cm-2 when x = 0.4. XRD measurements revealed high temperature stability and CO2-tolerant property of the dual-phase composites. The partial replacement of Fe$^{3+}$/Fe$^{4+}$ by Al$^{3+}$ causes the material not only to exhibit good stability, but also to increase the oxygen permeability of the membranes.
Developing good performance and low-cost oxygen permeable membranes for CO2 capture based on the oxy-fuel concept is greatly desirable but challenging. Despite tremendous efforts in exploring new CO2-stable dual-phase membranes, its presence is however still far from meeting the industrial requirements. Here we report a series of new Ca-containing CO2-resistant oxygen transporting membranes with composition 60wt.%Ce0.9Ln0.1O2-40wt.%Ln0.6Ca0.4FeO3(CLnO-LnCFO; Ln = La, Pr, Nd, Sm) synthesized via a Pechini one-pot method. Our results indicate all investigated compounds are composed of perovskite and fluorite phases, while the perovskite phases in the CNO-NCFO and CSO-SCFO membranes after sintering generates Ca-rich and Ca-less two kinds of grains with different morphologies, where the Ca-less small perovskite grains block the transport of oxygen ions and eventually result in poor oxygen permeability. Among our investigated CLnO-LnCFO membranes, CPO-PCFO exhibits the highest oxygen permeability and excellent CO2 stability, which were mainly associated with the improvement in crystal symmetry, non-negligible electronic conductivity of fluorite phase and the enhancement in electronic conductivity of perovskite. Our results establish Ca-containing oxides as candidate material platforms for membrane engineering devices that combine CO2 capture and oxygen separation.
Polymeric membranes, including Polysulfone (PSf) membranes, are routinely used for water treatment. It is known for quite some time that water permeability of above membranes can be improved if one incorporates carbon nanotubes (single-walled, SWCNTs or multi-walled, MWCNTs) in to the membrane and aligns them in direction of flow of water. This paper reports a method of synthesizing polymeric membranes having vertically aligned hollow CNTs embedded in them. This involves mixing of nanomagnetic particles in the dope solution and casting of membrane in presence of moderate magnetic fields. A semi-automatic membrane casting machine which allows casting of membrane in presence magnetic field was designed and fabricated. PSf nanocomposite membranes, having vertically aligned MWCNTSs, were synthesized using above machine. The effect of magnetic field and the exposure time on the water permeation of above membranes was studied. It was seen that water permeability of membrane increases by a factor of 4 when the magnetic field is increased from 0 to 1500 Gauss. There was additional 40% increase in water permeability, when the time for which film was exposed to magnetic field was increased from 5 sec. to 10 sec.
Delta ($delta$) phase comprising polyvinylidene fluoride (PVDF) nanoparticles are fabricated through electrospray technique by applying 0.1 MV/m electric field at ambient temperature and pressure, which is 10$^{3}$ times lower than the typical value, required for $delta$-phase transformation. The X-ray diffraction (XRD) and selected area electron diffraction (SAED) patterns are clearly indicating the $delta$-phase formation. The piezo- and ferro- electric response of the $delta$-PVDF nanoparticles has been demonstrated through scanning probe microscopic technique based on piezoresponse force microscopy (PFM). The vertical piezoelectric response, indicated by d$_{33}$ coefficient, is found $sim$-11 pm/V. Kink propagation model is adopted to justify the $delta$-phase conversion in electrospray system. The electrical response from $delta$-PVDF nanoparticle comprised nanogenerator under the external impacts and acoustic signal indicates that molecular ferroelectric dipoles responsible for piezoelectric responses, are poled in-situ during nanoparticle formation, thus further electrical poling is not necessary.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
