The oxidative dehydrogenation （ODH） reactions of ethane and propane were investigated in a catalytic membrane reactor, incorporating oxygen-permeable membranes based upon La2Ni0.9V0.1O4＋δor Ba0.5Sr0.5Co0.8Fe0.2O3-...The oxidative dehydrogenation （ODH） reactions of ethane and propane were investigated in a catalytic membrane reactor, incorporating oxygen-permeable membranes based upon La2Ni0.9V0.1O4＋δor Ba0.5Sr0.5Co0.8Fe0.2O3-δ. As a compromise between the occurrence of a measureable oxygen flux and excessive homogenous gas phase reactions, the measurements were conducted at an intermediate temperature, either at 550 or 650 oC. The results show the dominating role of the oxygen flux across the membrane and available sites at the membrane surface in primary activation of the alkane and, hence, in achieving high alkane conversions. The experimental data of ODH of propane and ethane on both membrane materials can be reconciled on the basis of Mars-van Krevelen mechanism, in which the alkane reacts with lattice oxygen on the membrane surface to produce the corresponding olefin. It is further demonstrated that the oxygen concentration in the gas phase and on the membrane surface is crucial for determining the olefin selectivity.展开更多
The process parameters were optimized for the eleetrodeposition of nickel in an electrolytic membrane reactor. Nickel（Ⅱ） and boric acid concentrations, pH and temperature were varied to evaluate the changes in curr...The process parameters were optimized for the eleetrodeposition of nickel in an electrolytic membrane reactor. Nickel（Ⅱ） and boric acid concentrations, pH and temperature were varied to evaluate the changes in current efficiency and specific energy consumption of nickel electrodeposition. The catholyte was aqueous nickel（Ⅱ） sulfate and boric acid, and the anolyte was sulfuric acid solution. An anionic membrane separated the anolyte from the catholyte while maintained a conductive path between the two compartments. The results indicated that the cathode current efficiency increased with the increase of nickel concentration, pH and boric acid concentration, and decreased with the increase of current density and stirring rate. A maximum current efficiency of 97.15% was obtained under the optimized conditions of electrolyte composition of 40 g/L Ni and 40 g/L boric acid at temperature of 42 ℃ and pH of 6 with a cathode current density of 300 A/m2.展开更多
A recombinant human androgen receptor yeast assay was applied to investigate the occurrence of antiandrogens as well as the mechanism for their removal during gray wastewater and coking wastewater treatment. The membr...A recombinant human androgen receptor yeast assay was applied to investigate the occurrence of antiandrogens as well as the mechanism for their removal during gray wastewater and coking wastewater treatment. The membrane reactor（MBR） system for gray wastewater treatment could remove 88.0% of antiandrogenic activity exerted by weakly polar extracts and 97.3% of that by moderately strong polar extracts, but only 32.5%of that contributed by strong polar extracts. Biodegradation by microorganisms in the MBR contributed to 95.9% of the total removal. After the treatment, the concentration of antiandrogenic activity in the effluent was still 1.05 μg flutamide equivalence（FEQ）/L, 36.2%of which was due to strong polar extracts. In the anaerobic reactor, anoxic reactor, and membrane reactor system for coking wastewater treatment, the antiandrogenic activity of raw coking wastewater was 78.6 mg FEQ/L, and the effluent of the treatment system had only 0.34 mg FEQ/L. The antiandrogenic activity mainly existed in the medium strong polar and strong polar extracts. Biodegradation by microorganisms contributed to at least 89.2%of the total antiandrogenic activity removal in the system. Biodegradation was the main removal mechanism of antiandrogenic activity in both the wastewater treatment systems.展开更多
Heterogeneous catalysts with ultrafine or nano particle size have currently attracted considerable attentions in the chemical and petrochemical production processes, but their large-scale applications remain challengi...Heterogeneous catalysts with ultrafine or nano particle size have currently attracted considerable attentions in the chemical and petrochemical production processes, but their large-scale applications remain challenging because of difficulties associated with their efficient separation from the reaction slurry. A porous ceramic membrane reactor has emerged as a promising method to solve the problem concerning catalysts separation in situ from the reaction mixture and make the production process continuous in heterogeneous catalysis. This article presents a review of the present progress on porous ceramic membrane reactors for heterogeneous catalysis, which covers classification of configurations of porous ceramic membrane reactor, major considerations and some important industrial applications. A special emphasis is paid to major considerations in term of application-oriented ceramic membrane design, optimization of ceramic membrane reactor performance and membrane fouling mechanism. Finally, brief concluding remarks on porous ceramic membrane reactors are given and possible future research interests are also outlined.展开更多
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...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.展开更多
The catalyst function was achieved in two regions in an oxygen permeation membrane reactor： H2 dissociated and reacted with lattice oxygen or oxygen ions to form H20 near the membrane surface. The H20 formed could re...The catalyst function was achieved in two regions in an oxygen permeation membrane reactor： H2 dissociated and reacted with lattice oxygen or oxygen ions to form H20 near the membrane surface. The H20 formed could react with the residual CH4 away from the membrane surface area.展开更多
The performance of LiNi/γ-Al2O3 catalysts modified by rare earth metal oxide （La2O3 or CeO2） packed on BCFNO membrane reactor was discussed for the partial oxidation of methane （POM） in coke oven gas （COG） at 8...The performance of LiNi/γ-Al2O3 catalysts modified by rare earth metal oxide （La2O3 or CeO2） packed on BCFNO membrane reactor was discussed for the partial oxidation of methane （POM） in coke oven gas （COG） at 875 ℃. The NiO/γ-Al2O3 catalysts with different amounts of La2O3 and CeO2 were prepared with the same preparation method and under the same condition in order to compare the reaction performance （oxygen permeation, CH4 conversion, H2 and CO selectivity） on the membrane reactor. The results show that the oxygen permeation flux increased significantly with LiNiREOx/γ-Al2O3 （RE = La or Ce） catalysts by adding the element of rare earth especially the Ce during the POM in COG. Such as, the Li15wt%CeO29wt%NiO/γ-Al2O3 catalyst with an oxygen permeation flux of 24.71 ml·cm^-2·min^-1 and a high CH4 conversion was obtained in 875 ℃. The resulted high oxygen permeation flux may be due to the added Ce that inhibited the strong interaction between Ni and Al2O3 to form the NiAl2O4 phase. In addition, the introduction of Ce leads up to an important property of storing and releasing oxygen.展开更多
Ba0.5Sr0.5Co0.8Fe0.1Ni0.1O3δ（BSCFNiO） perovskite oxides were synthesized using a combined EDTA-citrate complexation method,and then pressed into disk and applied in a membrane reactor.The performance of the BSCFNiO...Ba0.5Sr0.5Co0.8Fe0.1Ni0.1O3δ（BSCFNiO） perovskite oxides were synthesized using a combined EDTA-citrate complexation method,and then pressed into disk and applied in a membrane reactor.The performance of the BSCFNiO membrane reactor was studied for partial oxidation of methane over Ni/α-Al 2 O 3 catalyst.The time dependence of oxygen permeation rate and catalytic performance of BSCFNiO membrane during the catalyst initiation stage were investigated at 850 C.In unsteady state,oxygen permeation rate,methane conversion and CO selectivity were closely related to the state of the catalyst.After 300 min from the initial time,the reaction condition reached to steady state and oxygen permeation rate were obtained about 11.7cm 3 cm 2 min 1.Also,the performance of membrane reactor was studied at the temperatures between 750 and 950 C.The results demonstrated good performance for the membrane reactor,as CH 4 conversion and CO selectivity permeation rate reached 98% and 97.5%,respectively,and oxygen permeation rate was about 14.5 cm 3 cm 2 min 1 which was 6.8 times higher than that of air-helium gradient.Characterization of membrane surface by SEM after reaction showed that the original grains disappeared on both surfaces exposed to the air and reaction side,but XRD profile of the polished surface membrane indicated that the membrane bulk preserved the perovskite structure.展开更多
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...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.展开更多
A functional electrocatalytic membrane reactor(ECMR) was performed for the electrocatalytic oxidation of2,2,3,3-tetrafluoro-l-propanol(TFP) into high value-added sodium 2,2,3,3-tetrafluoropropionate(STFP),A computatio...A functional electrocatalytic membrane reactor(ECMR) was performed for the electrocatalytic oxidation of2,2,3,3-tetrafluoro-l-propanol(TFP) into high value-added sodium 2,2,3,3-tetrafluoropropionate(STFP),A computational fluid dynamics(CFD) technique was applied to simulate the hydrodynamic distributions along a tubular ECMR so as to provide guidance for the design and optimization of ECMR Two-dimensional simulation with porous media model was employed to predict the properties of fluid dynamics in ECMR.The experimental investigation was carried to confirm the CFD simulation.Results showed that a uniform distribution of permeate velocity along the tubular reactor with short length and large diameter could be obtained.TFP conversion of97.7%,the selectivity to STFP of 99.9%and current efficiency of 40.1%were achieved from the ECMR with a length of 40 mm and an inside diameter of 53 mm.The simulations were in good agreement with the experimental results.展开更多
Polyaluminum chloride was synthesized with a membrane reactor,in which NaOH was added into AlCl 3 solution through the membrane’s micropores to reduce the NaOH droplets size.The content of the most efficient species ...Polyaluminum chloride was synthesized with a membrane reactor,in which NaOH was added into AlCl 3 solution through the membrane’s micropores to reduce the NaOH droplets size.The content of the most efficient species increased to about 80%.The process characteristics in the reaction （i.e.,flow velocity,pressure drop）,and membrane fouling and cleaning were investigated.The evolution of both flow velocity and pressure drop during the reaction were related to changes in species distribution and solution viscosity.The process characteristics were well interpreted in terms of the Bernoulli equation.After reaction,the membranes were recovered by cleaning with diluted hydrochloride acid.This study is crucial for process design and scale-up of membrane reactors.展开更多
CH4-CO2-O-2 reforming to syngas in a never Ba0.5Sr0.5Co0.8Fe0.2O3.delta oxygen-permeable membrane reactor using LiLaNiO/gamma-Al2O3 as catalyst was successfully reported. Excellent reaction performance was achieved wi...CH4-CO2-O-2 reforming to syngas in a never Ba0.5Sr0.5Co0.8Fe0.2O3.delta oxygen-permeable membrane reactor using LiLaNiO/gamma-Al2O3 as catalyst was successfully reported. Excellent reaction performance was achieved with around 92% methane conversion efficiency, 95% CO2 conversion rate, and nearly 8.5mL/min.cm(2) oxygen permeation flux. In contrast to the oxygen permeation model with the presence of large concentration of CO2 (under such condition the oxygen permeation flux deteriorates with time), the oxygen permeation flux is really stable under the CH4CO2-O-2 reforming condition.展开更多
The effects of temperature and pressure on the steam reforming of methane （CH4＋H2O→← 3H2＋CO） were investigated in a membrane reactor （MR） with a hydrogen permeable membrane. The studies used a novel silica-bas...The effects of temperature and pressure on the steam reforming of methane （CH4＋H2O→← 3H2＋CO） were investigated in a membrane reactor （MR） with a hydrogen permeable membrane. The studies used a novel silica-based membrane prepared by using the chemical vapor deposition （CVD） technique with a permeance for H2 of 6.0×10^-8 mol·m^-2.s^-1.Pa^-1 at 923 K. The results in a packed-bed reactor （PBR） were compared to those of the membrane reactor at various temperatures （773-923 K） and pressures （1-20 atm, 101.3-2026.5 kPa） using a commercial Ni/MgAl2O4 catalyst. The conversion of methane was improved significantly in the MR by the countercurrent removal of hydrogen at all temperatures and allowed product yields higher than the equilibrium to be obtained. Pressure had a positive effect on the hydrogen yield because of the increase in driving force for the permeance of hydrogen. The yield of hydrogen increased with pressure and reached a value of 73× 10^-6 mol·g^-1 .s^-1 at 2026.5 kPa and 923 K which was higher by 108% than the value of 35×10^-6 mol·g^-1.s^-1 obtained for the equilibrium yield. The results obtained with the silica-based membrane were similar to those obtained with various other membranes as reported in the literature.展开更多
Provskite-type catalysts, Ln0.6 Sr0.4 FexCo1-x O3 (Ln = Nd,Pr, Gd, Sm, La, 0＜x＜1) and Ln0.8Na0.2CoO3(Ln= La,Gd, Sm) were synthesized, their catalytic properties in the oxidative coupling of methane (OCM) were examin...Provskite-type catalysts, Ln0.6 Sr0.4 FexCo1-x O3 (Ln = Nd,Pr, Gd, Sm, La, 0＜x＜1) and Ln0.8Na0.2CoO3(Ln= La,Gd, Sm) were synthesized, their catalytic properties in the oxidative coupling of methane (OCM) were examined in a fixed-bed reactor. The former group presented higher activity in the OCM, but the main product was carbon dioxide. While the later group showed lower activity but much higher selectivity to C2 hydrocarbons compared with the former. Electrochemical measurements were conducted in a solid oxide membrane reactor with La0.8 Na0.2CoO3 as catalyst. The results showed that methane was oxidized to carbon dioxide and ethane by two parallel reactions. Ethane was oxidized to ethene and carbon dioxide. A fraction of ethene was oxidized deeply to carbon dioxide. The total selectivity to C2 hydrocarbons exceeded 70%. Based on the experimental results, a kinetic model was suggested to describe the reaction results.展开更多
A two-dimensional non-isothermal mathematical model has been developed for the ethane dehydrogenation reaction in a fixed-bed catalytic membrane reactor. Since ethane dehydrogenation is an equilibrium reaction,removal...A two-dimensional non-isothermal mathematical model has been developed for the ethane dehydrogenation reaction in a fixed-bed catalytic membrane reactor. Since ethane dehydrogenation is an equilibrium reaction,removal of produced hydrogen by the membrane shifts the thermodynamic equilibrium to ethylene production.For further displacement of the dehydrogenation reaction, oxidative dehydrogenation method has been used.Since ethane dehydrogenation is an endothermic reaction, the energy produced by the oxidative dehydrogenation method is consumed by the dehydrogenation reaction. The results show that the oxidative dehydrogenation method generated a substantial improvement in the reactor performance in terms of high conversions and signi ficant energy saving. It was also established that the sweep gas velocity in the shell side of the reactor is one of the most important factors in the effectiveness of the reactor.展开更多
Partial oxidation of methane（POM） co-fed with CO_2 to syngas in a novel catalytic BaCo_（0.6）Fe_（0.2）Ta_（0.2）O_（3-δ） oxygen permeable membrane reactor was successfully reported.Adding CO_2 to the partial oxi...Partial oxidation of methane（POM） co-fed with CO_2 to syngas in a novel catalytic BaCo_（0.6）Fe_（0.2）Ta_（0.2）O_（3-δ） oxygen permeable membrane reactor was successfully reported.Adding CO_2 to the partial oxidation of methane reaction not only alters the ratio of CO/H_2,but also increases the oxygen permeation flux and CH_4 conversion.Around 96%CH_4 conversion with more than 93%CO_2 conversion and 100%CO selectivity is achieved,which shows an excellent reaction performance.A steady oxygen permeation flux of 15 mL/（cm^2 min） is obtained during the 100-h operation,which shows good stability as well.展开更多
The oxidative dehydrogenation of butane to butadiene and butene was studied using a conventional fixed-bed ractor (FBR), inert membrane reactor (IMR) and mixed inert membrane reactor (MIMR). When IMR and MIMR were emp...The oxidative dehydrogenation of butane to butadiene and butene was studied using a conventional fixed-bed ractor (FBR), inert membrane reactor (IMR) and mixed inert membrane reactor (MIMR). When IMR and MIMR were employed, a ceramic membrane modified by partially coating with glaze was used to distribute oxygen to a fixed-bed of 24-V-Mg-O catalyst. The oxygen partial pressure in the catalyst bed could be decreased. The effect of feeding modes and operation conditions were investigated. The selectivity of C4 dehydrogenation products (butene and butadiene) was found to be higher in IMR than in FBR. The feeding mode with 20% of air mixing with butane in MIMR was found to be more efficient than the feeding mode with all air permeating through ceramic membrane. The MIMR gave the most smooth temperature profile along the bed.展开更多
Ethylene,one of the most widely produced building blocks in the petrochemical industry,has received intense attention.Ethylene production,using electrochemical hydrogen pump-facilitated nonoxidative dehydrogenation of...Ethylene,one of the most widely produced building blocks in the petrochemical industry,has received intense attention.Ethylene production,using electrochemical hydrogen pump-facilitated nonoxidative dehydrogenation of ethane(NDE)to ethylene,is an emerging and promising route,promoting the transformation of the ethylene industry from energy-intensive steam cracking process to new electrochemical membrane reactor technology.In this work,the NDE reaction is incorporated into a BaZr_(0.1)Ce_(0.7)Y_(0.1)Yb_(0.1)O_(3-δ)electrolyte-supported protonic ceramic fuel cell membrane reactor to co-generate electricity and ethylene,utilizing the Nb and Cu doped perovskite oxide Pr_(0.6)Sr_(0.4)Fe_(0.8)Nb_(0.1)Cu_(0.1)O_(3-δ)(PSFNCu)as anode catalytic layer.Due to the doping of Nb and Cu,PSFNCu was endowed with high reduction tolerance and rich oxygen vacancies,showing excellent NDE catalytic performance.The maximum power density of the assembled reactor reaches 200 mW cm^(-2)at 750℃,with high ethane conversion(44.9%)and ethylene selectivity(92.7%).Moreover,the nitrous oxide decomposition was first coupled in the protonic ceramic fuel cell membrane reactor to consume the permeated protons.As a result,the generation of electricity,ethylene and decomposition of nitrous oxide can be simultaneously obtained by a single reactor.Specifically,the maximum power density of the cell reaches 208 mW cm^(-2)at 750℃,with high ethane conversion(45.2%),ethylene selectivity(92.5%),and nitrous oxide conversion(19,0%).This multi-win technology is promising for not only the production of chemicals and energy but also greenhouse gas reduction.展开更多
A two-stage catalytic membrane reactor(CMR)that couples CO_(2) splitting with methane oxidation reactions was constructed based on an oxygen-permeable perovskite asymmetric membrane.The asymmetric membrane comprises a...A two-stage catalytic membrane reactor(CMR)that couples CO_(2) splitting with methane oxidation reactions was constructed based on an oxygen-permeable perovskite asymmetric membrane.The asymmetric membrane comprises a dense SrFe_(0.9)Ta_(0.1)O_(3-σ)(SFT)separation layer and a porous Sr_(0.9)(Fe_(0.9)Ta_(0.1))_(0.9)Cu_(0.1)O_(3-σ)(SFTC)catalytic layer.In thefirst stage reactor,a CO_(2) splitting reaction(CDS:2CO_(2)→2CO+O_(2))occurs at the SFTC catalytic layer.Subsequently,the O_(2) product is selectively extracted through the SFT separation layer to the permeated side for the methane combustion reaction(MCR),which provides an extremely low oxygen partial pressure to enhance the oxygen extraction.In the second stage,a Sr_(0.9)(Fe_(0.9)Ta_(0.1))_(0.9)Ni_(0.1)O_(3-σ)(SFTN)catalyst is employed to reform the products derived from MCR.The two-stage CMR design results in a remarkable 35.4%CO_(2) conversion for CDS at 900℃.The two-stage CMR was extended to a hollowfiber configuration combining with solar irradiation.The solar-assisted two-stage CMR can operate stably for over 50 h with a high hydrogen yield of 18.1 mL min^(-1) cm^(-2).These results provide a novel strategy for reducing CO_(2) emissions,suggesting potential avenues for the design of the high-performance CMRs and catalysts based on perovskite oxides in the future.展开更多
In this paper, the effect of water vapor removal on methanol synthesis capacity from syngas in a fixed-bed membrane reactor is studied considering long-term catalyst deactivation. A dynamic heterogeneous one-dimension...In this paper, the effect of water vapor removal on methanol synthesis capacity from syngas in a fixed-bed membrane reactor is studied considering long-term catalyst deactivation. A dynamic heterogeneous one-dimensional mathematical model that is composed of two sides is developed to predict the performance of this configuration. In this configuration, conventional methanol reactor is supported by an aluminasilica composite membrane layer for water vapor removal from reaction zone. To verify the accuracy of the considered model and assumptions, simulation results of the conventional methanol reactor is compared with the industrial plant data under the same process condition. The membrane reactor improves catalyst life time and enhances CO2 conversion to methanol by overcoming the limitation imposed by thermodynamic equilibrium. This configuration has enhanced the methanol production capacity about 4.06% compared with the industrial methanol reactor during the production time.展开更多
文摘The oxidative dehydrogenation （ODH） reactions of ethane and propane were investigated in a catalytic membrane reactor, incorporating oxygen-permeable membranes based upon La2Ni0.9V0.1O4＋δor Ba0.5Sr0.5Co0.8Fe0.2O3-δ. As a compromise between the occurrence of a measureable oxygen flux and excessive homogenous gas phase reactions, the measurements were conducted at an intermediate temperature, either at 550 or 650 oC. The results show the dominating role of the oxygen flux across the membrane and available sites at the membrane surface in primary activation of the alkane and, hence, in achieving high alkane conversions. The experimental data of ODH of propane and ethane on both membrane materials can be reconciled on the basis of Mars-van Krevelen mechanism, in which the alkane reacts with lattice oxygen on the membrane surface to produce the corresponding olefin. It is further demonstrated that the oxygen concentration in the gas phase and on the membrane surface is crucial for determining the olefin selectivity.
文摘The process parameters were optimized for the eleetrodeposition of nickel in an electrolytic membrane reactor. Nickel（Ⅱ） and boric acid concentrations, pH and temperature were varied to evaluate the changes in current efficiency and specific energy consumption of nickel electrodeposition. The catholyte was aqueous nickel（Ⅱ） sulfate and boric acid, and the anolyte was sulfuric acid solution. An anionic membrane separated the anolyte from the catholyte while maintained a conductive path between the two compartments. The results indicated that the cathode current efficiency increased with the increase of nickel concentration, pH and boric acid concentration, and decreased with the increase of current density and stirring rate. A maximum current efficiency of 97.15% was obtained under the optimized conditions of electrolyte composition of 40 g/L Ni and 40 g/L boric acid at temperature of 42 ℃ and pH of 6 with a cathode current density of 300 A/m2.
基金funded by the National High-Tech Research and Development Program (863 Program) of China (No. 2013AA062705-1)the National Natural Science Funds of China (No. 51308319)
文摘A recombinant human androgen receptor yeast assay was applied to investigate the occurrence of antiandrogens as well as the mechanism for their removal during gray wastewater and coking wastewater treatment. The membrane reactor（MBR） system for gray wastewater treatment could remove 88.0% of antiandrogenic activity exerted by weakly polar extracts and 97.3% of that by moderately strong polar extracts, but only 32.5%of that contributed by strong polar extracts. Biodegradation by microorganisms in the MBR contributed to 95.9% of the total removal. After the treatment, the concentration of antiandrogenic activity in the effluent was still 1.05 μg flutamide equivalence（FEQ）/L, 36.2%of which was due to strong polar extracts. In the anaerobic reactor, anoxic reactor, and membrane reactor system for coking wastewater treatment, the antiandrogenic activity of raw coking wastewater was 78.6 mg FEQ/L, and the effluent of the treatment system had only 0.34 mg FEQ/L. The antiandrogenic activity mainly existed in the medium strong polar and strong polar extracts. Biodegradation by microorganisms contributed to at least 89.2%of the total antiandrogenic activity removal in the system. Biodegradation was the main removal mechanism of antiandrogenic activity in both the wastewater treatment systems.
基金Supported by the National Natural Science Foundation of China （20990222, 21106061）, the National Basic Research Program of China （2009CB623406）, the National Key Science and Technology Program of China （2011BAE07B05） and the Natural Science Foundation of Jiangsu Province, China （BK2010549, BK2009021）.
文摘Heterogeneous catalysts with ultrafine or nano particle size have currently attracted considerable attentions in the chemical and petrochemical production processes, but their large-scale applications remain challenging because of difficulties associated with their efficient separation from the reaction slurry. A porous ceramic membrane reactor has emerged as a promising method to solve the problem concerning catalysts separation in situ from the reaction mixture and make the production process continuous in heterogeneous catalysis. This article presents a review of the present progress on porous ceramic membrane reactors for heterogeneous catalysis, which covers classification of configurations of porous ceramic membrane reactor, major considerations and some important industrial applications. A special emphasis is paid to major considerations in term of application-oriented ceramic membrane design, optimization of ceramic membrane reactor performance and membrane fouling mechanism. Finally, brief concluding remarks on porous ceramic membrane reactors are given and possible future research interests are also outlined.
基金supported by the National High Technology Research and Development Program of China (Grant No. 2006AA11A189)Science and Technology Commission of Shanghai Municipality (Grant Nos. 0952NM01400 and 07DZ12036)
文摘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.
基金supported by the Natural Science Foundation of China(Grant No.51304082 and 51174133)the Natural Science Foundation of Jiangsu Province,China(Grant No.BK20130462)+1 种基金the Natural Science Foundation of the Jiangsu Higher Education Institutions of China(Grant No.12KJB450001)the Science and Technology Commission of Shanghai Municipality(Grant No.11ZR1412900)
文摘The catalyst function was achieved in two regions in an oxygen permeation membrane reactor： H2 dissociated and reacted with lattice oxygen or oxygen ions to form H20 near the membrane surface. The H20 formed could react with the residual CH4 away from the membrane surface area.
基金supported by the National High Technology Research and Development Program of China (No. 2006AA11A189)Science and Technology Commission of Shanghai Municipality (No. 06DZ12212)+1 种基金National Engineering Research Center of Advanced Steel Technology (NERCAST) (No. 050209)the Innovation Fund for Graduate Studentof Shanghai University (SHUCX0910003)
文摘The performance of LiNi/γ-Al2O3 catalysts modified by rare earth metal oxide （La2O3 or CeO2） packed on BCFNO membrane reactor was discussed for the partial oxidation of methane （POM） in coke oven gas （COG） at 875 ℃. The NiO/γ-Al2O3 catalysts with different amounts of La2O3 and CeO2 were prepared with the same preparation method and under the same condition in order to compare the reaction performance （oxygen permeation, CH4 conversion, H2 and CO selectivity） on the membrane reactor. The results show that the oxygen permeation flux increased significantly with LiNiREOx/γ-Al2O3 （RE = La or Ce） catalysts by adding the element of rare earth especially the Ce during the POM in COG. Such as, the Li15wt%CeO29wt%NiO/γ-Al2O3 catalyst with an oxygen permeation flux of 24.71 ml·cm^-2·min^-1 and a high CH4 conversion was obtained in 875 ℃. The resulted high oxygen permeation flux may be due to the added Ce that inhibited the strong interaction between Ni and Al2O3 to form the NiAl2O4 phase. In addition, the introduction of Ce leads up to an important property of storing and releasing oxygen.
文摘Ba0.5Sr0.5Co0.8Fe0.1Ni0.1O3δ（BSCFNiO） perovskite oxides were synthesized using a combined EDTA-citrate complexation method,and then pressed into disk and applied in a membrane reactor.The performance of the BSCFNiO membrane reactor was studied for partial oxidation of methane over Ni/α-Al 2 O 3 catalyst.The time dependence of oxygen permeation rate and catalytic performance of BSCFNiO membrane during the catalyst initiation stage were investigated at 850 C.In unsteady state,oxygen permeation rate,methane conversion and CO selectivity were closely related to the state of the catalyst.After 300 min from the initial time,the reaction condition reached to steady state and oxygen permeation rate were obtained about 11.7cm 3 cm 2 min 1.Also,the performance of membrane reactor was studied at the temperatures between 750 and 950 C.The results demonstrated good performance for the membrane reactor,as CH 4 conversion and CO selectivity permeation rate reached 98% and 97.5%,respectively,and oxygen permeation rate was about 14.5 cm 3 cm 2 min 1 which was 6.8 times higher than that of air-helium gradient.Characterization of membrane surface by SEM after reaction showed that the original grains disappeared on both surfaces exposed to the air and reaction side,but XRD profile of the polished surface membrane indicated that the membrane bulk preserved the perovskite structure.
基金supported by the National High Technology Research and Development Program of China (Project No. 2006AA11A189)
文摘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.
基金Supported by the National Natural Science Foundation of China(21206119 and21576208)the Program for Changjiang Scholars and Innovative Research Team in University of Ministry of Education of China(IRT13084)
文摘A functional electrocatalytic membrane reactor(ECMR) was performed for the electrocatalytic oxidation of2,2,3,3-tetrafluoro-l-propanol(TFP) into high value-added sodium 2,2,3,3-tetrafluoropropionate(STFP),A computational fluid dynamics(CFD) technique was applied to simulate the hydrodynamic distributions along a tubular ECMR so as to provide guidance for the design and optimization of ECMR Two-dimensional simulation with porous media model was employed to predict the properties of fluid dynamics in ECMR.The experimental investigation was carried to confirm the CFD simulation.Results showed that a uniform distribution of permeate velocity along the tubular reactor with short length and large diameter could be obtained.TFP conversion of97.7%,the selectivity to STFP of 99.9%and current efficiency of 40.1%were achieved from the ECMR with a length of 40 mm and an inside diameter of 53 mm.The simulations were in good agreement with the experimental results.
基金supported by the National Natural Sci-ences Foundation of China(No.50072042,20676016,21076024)
文摘Polyaluminum chloride was synthesized with a membrane reactor,in which NaOH was added into AlCl 3 solution through the membrane’s micropores to reduce the NaOH droplets size.The content of the most efficient species increased to about 80%.The process characteristics in the reaction （i.e.,flow velocity,pressure drop）,and membrane fouling and cleaning were investigated.The evolution of both flow velocity and pressure drop during the reaction were related to changes in species distribution and solution viscosity.The process characteristics were well interpreted in terms of the Bernoulli equation.After reaction,the membranes were recovered by cleaning with diluted hydrochloride acid.This study is crucial for process design and scale-up of membrane reactors.
文摘CH4-CO2-O-2 reforming to syngas in a never Ba0.5Sr0.5Co0.8Fe0.2O3.delta oxygen-permeable membrane reactor using LiLaNiO/gamma-Al2O3 as catalyst was successfully reported. Excellent reaction performance was achieved with around 92% methane conversion efficiency, 95% CO2 conversion rate, and nearly 8.5mL/min.cm(2) oxygen permeation flux. In contrast to the oxygen permeation model with the presence of large concentration of CO2 (under such condition the oxygen permeation flux deteriorates with time), the oxygen permeation flux is really stable under the CH4CO2-O-2 reforming condition.
文摘The effects of temperature and pressure on the steam reforming of methane （CH4＋H2O→← 3H2＋CO） were investigated in a membrane reactor （MR） with a hydrogen permeable membrane. The studies used a novel silica-based membrane prepared by using the chemical vapor deposition （CVD） technique with a permeance for H2 of 6.0×10^-8 mol·m^-2.s^-1.Pa^-1 at 923 K. The results in a packed-bed reactor （PBR） were compared to those of the membrane reactor at various temperatures （773-923 K） and pressures （1-20 atm, 101.3-2026.5 kPa） using a commercial Ni/MgAl2O4 catalyst. The conversion of methane was improved significantly in the MR by the countercurrent removal of hydrogen at all temperatures and allowed product yields higher than the equilibrium to be obtained. Pressure had a positive effect on the hydrogen yield because of the increase in driving force for the permeance of hydrogen. The yield of hydrogen increased with pressure and reached a value of 73× 10^-6 mol·g^-1 .s^-1 at 2026.5 kPa and 923 K which was higher by 108% than the value of 35×10^-6 mol·g^-1.s^-1 obtained for the equilibrium yield. The results obtained with the silica-based membrane were similar to those obtained with various other membranes as reported in the literature.
基金This work was supported supported by the Center Petrochemical Company of China (X599027).
文摘Provskite-type catalysts, Ln0.6 Sr0.4 FexCo1-x O3 (Ln = Nd,Pr, Gd, Sm, La, 0＜x＜1) and Ln0.8Na0.2CoO3(Ln= La,Gd, Sm) were synthesized, their catalytic properties in the oxidative coupling of methane (OCM) were examined in a fixed-bed reactor. The former group presented higher activity in the OCM, but the main product was carbon dioxide. While the later group showed lower activity but much higher selectivity to C2 hydrocarbons compared with the former. Electrochemical measurements were conducted in a solid oxide membrane reactor with La0.8 Na0.2CoO3 as catalyst. The results showed that methane was oxidized to carbon dioxide and ethane by two parallel reactions. Ethane was oxidized to ethene and carbon dioxide. A fraction of ethene was oxidized deeply to carbon dioxide. The total selectivity to C2 hydrocarbons exceeded 70%. Based on the experimental results, a kinetic model was suggested to describe the reaction results.
文摘A two-dimensional non-isothermal mathematical model has been developed for the ethane dehydrogenation reaction in a fixed-bed catalytic membrane reactor. Since ethane dehydrogenation is an equilibrium reaction,removal of produced hydrogen by the membrane shifts the thermodynamic equilibrium to ethylene production.For further displacement of the dehydrogenation reaction, oxidative dehydrogenation method has been used.Since ethane dehydrogenation is an endothermic reaction, the energy produced by the oxidative dehydrogenation method is consumed by the dehydrogenation reaction. The results show that the oxidative dehydrogenation method generated a substantial improvement in the reactor performance in terms of high conversions and signi ficant energy saving. It was also established that the sweep gas velocity in the shell side of the reactor is one of the most important factors in the effectiveness of the reactor.
基金the financial support by Natural Science Foundation of China(Nos.U0834004 and 20936001)the Science-Technology Plan of Guangzhou City(No.2009J1-C511-1)the Fundamental Research Funds for the Central Universities,SCUT(No.2009220038)
文摘Partial oxidation of methane（POM） co-fed with CO_2 to syngas in a novel catalytic BaCo_（0.6）Fe_（0.2）Ta_（0.2）O_（3-δ） oxygen permeable membrane reactor was successfully reported.Adding CO_2 to the partial oxidation of methane reaction not only alters the ratio of CO/H_2,but also increases the oxygen permeation flux and CH_4 conversion.Around 96%CH_4 conversion with more than 93%CO_2 conversion and 100%CO selectivity is achieved,which shows an excellent reaction performance.A steady oxygen permeation flux of 15 mL/（cm^2 min） is obtained during the 100-h operation,which shows good stability as well.
基金Supported by the National Natural Science Foundation of China(No.29776005).
文摘The oxidative dehydrogenation of butane to butadiene and butene was studied using a conventional fixed-bed ractor (FBR), inert membrane reactor (IMR) and mixed inert membrane reactor (MIMR). When IMR and MIMR were employed, a ceramic membrane modified by partially coating with glaze was used to distribute oxygen to a fixed-bed of 24-V-Mg-O catalyst. The oxygen partial pressure in the catalyst bed could be decreased. The effect of feeding modes and operation conditions were investigated. The selectivity of C4 dehydrogenation products (butene and butadiene) was found to be higher in IMR than in FBR. The feeding mode with 20% of air mixing with butane in MIMR was found to be more efficient than the feeding mode with all air permeating through ceramic membrane. The MIMR gave the most smooth temperature profile along the bed.
基金funding from the National Key R&D Program of China(2020YFB1505603)the Natural Science Foundation of China(22075086,22138005,22141001)the Guangdong Basic and Applied Basic Research Foundation(2019A1515011512,2020A1515011157,2021A1515010172,2022A1515010980)。
文摘Ethylene,one of the most widely produced building blocks in the petrochemical industry,has received intense attention.Ethylene production,using electrochemical hydrogen pump-facilitated nonoxidative dehydrogenation of ethane(NDE)to ethylene,is an emerging and promising route,promoting the transformation of the ethylene industry from energy-intensive steam cracking process to new electrochemical membrane reactor technology.In this work,the NDE reaction is incorporated into a BaZr_(0.1)Ce_(0.7)Y_(0.1)Yb_(0.1)O_(3-δ)electrolyte-supported protonic ceramic fuel cell membrane reactor to co-generate electricity and ethylene,utilizing the Nb and Cu doped perovskite oxide Pr_(0.6)Sr_(0.4)Fe_(0.8)Nb_(0.1)Cu_(0.1)O_(3-δ)(PSFNCu)as anode catalytic layer.Due to the doping of Nb and Cu,PSFNCu was endowed with high reduction tolerance and rich oxygen vacancies,showing excellent NDE catalytic performance.The maximum power density of the assembled reactor reaches 200 mW cm^(-2)at 750℃,with high ethane conversion(44.9%)and ethylene selectivity(92.7%).Moreover,the nitrous oxide decomposition was first coupled in the protonic ceramic fuel cell membrane reactor to consume the permeated protons.As a result,the generation of electricity,ethylene and decomposition of nitrous oxide can be simultaneously obtained by a single reactor.Specifically,the maximum power density of the cell reaches 208 mW cm^(-2)at 750℃,with high ethane conversion(45.2%),ethylene selectivity(92.5%),and nitrous oxide conversion(19,0%).This multi-win technology is promising for not only the production of chemicals and energy but also greenhouse gas reduction.
基金supported by the National Key Research and Development Program of China(2022YFE0101600)the National Natural Science Foundation of China(U23A20117)+2 种基金the Natural Science Foundation of Jiangsu Province(BK20220002,BE2022024)the Leading Talents Program of Zhejiang Province(2024C03223)Topnotch Academic Programs Project of Jiangsu Higher Education Institutions(TAPP).
文摘A two-stage catalytic membrane reactor(CMR)that couples CO_(2) splitting with methane oxidation reactions was constructed based on an oxygen-permeable perovskite asymmetric membrane.The asymmetric membrane comprises a dense SrFe_(0.9)Ta_(0.1)O_(3-σ)(SFT)separation layer and a porous Sr_(0.9)(Fe_(0.9)Ta_(0.1))_(0.9)Cu_(0.1)O_(3-σ)(SFTC)catalytic layer.In thefirst stage reactor,a CO_(2) splitting reaction(CDS:2CO_(2)→2CO+O_(2))occurs at the SFTC catalytic layer.Subsequently,the O_(2) product is selectively extracted through the SFT separation layer to the permeated side for the methane combustion reaction(MCR),which provides an extremely low oxygen partial pressure to enhance the oxygen extraction.In the second stage,a Sr_(0.9)(Fe_(0.9)Ta_(0.1))_(0.9)Ni_(0.1)O_(3-σ)(SFTN)catalyst is employed to reform the products derived from MCR.The two-stage CMR design results in a remarkable 35.4%CO_(2) conversion for CDS at 900℃.The two-stage CMR was extended to a hollowfiber configuration combining with solar irradiation.The solar-assisted two-stage CMR can operate stably for over 50 h with a high hydrogen yield of 18.1 mL min^(-1) cm^(-2).These results provide a novel strategy for reducing CO_(2) emissions,suggesting potential avenues for the design of the high-performance CMRs and catalysts based on perovskite oxides in the future.
文摘In this paper, the effect of water vapor removal on methanol synthesis capacity from syngas in a fixed-bed membrane reactor is studied considering long-term catalyst deactivation. A dynamic heterogeneous one-dimensional mathematical model that is composed of two sides is developed to predict the performance of this configuration. In this configuration, conventional methanol reactor is supported by an aluminasilica composite membrane layer for water vapor removal from reaction zone. To verify the accuracy of the considered model and assumptions, simulation results of the conventional methanol reactor is compared with the industrial plant data under the same process condition. The membrane reactor improves catalyst life time and enhances CO2 conversion to methanol by overcoming the limitation imposed by thermodynamic equilibrium. This configuration has enhanced the methanol production capacity about 4.06% compared with the industrial methanol reactor during the production time.
