Hydrate-based gas separation offers a promising approach for coalbed methane recovery,reaching energy conservation and emissions reduction.This study innovatively applied high-gravity technology to enhance hydrate for...Hydrate-based gas separation offers a promising approach for coalbed methane recovery,reaching energy conservation and emissions reduction.This study innovatively applied high-gravity technology to enhance hydrate formation in separating 25%CH_(4)/67%N_(2)/8%O_(2) for achieving rapid and efficient methane recovery.Systematic investigations were conducted at 283.2 K and 3.0 MPa with tetrahydrofuran at a molar concentration of 5.56%and L-tryptophan at a mass concentration of 0.5%additives,first evaluating liquid flow rate effects(0–20 mL/min)on mixed hydrate kinetic performance and separation efficiency,followed by rotating speed optimization(0–1200 r·min^(-1))under the optimal liquid flow rate.The high-gravity system amplified the gas–liquid contact area by~1155 times through cascaded liquid supply and secondary shear effects,methane molecules entered the hydrate phase rapidly under the highest driving force with the significantly intensified mass transfer.Optimal conditions(20 mL/min,600 r·min^(-1))yielded an exceptional initial hydrate growth rate of 58.59 mmol/(mol·h)and methane recovery of 50.76%,about 71.33 and 0.58 times higher than the static system,respectively.Gas chromatography and Raman spectrometer analyses revealed superior methane enrichment in hydrate phase at 90%gas uptake completion,with a concurrent 41.17%reduction in process duration.These findings demonstrate the efficacy of high-gravity-enhanced hydrate technology for coalbed methane separation,offering valuable insights for optimizing clean energy utilization.展开更多
The impregnation method for preparing catalysts often faces challenges such as prolonged preparation times and poor dispersion of active components due to the limited mobility of the impregnation liquid.The rotating p...The impregnation method for preparing catalysts often faces challenges such as prolonged preparation times and poor dispersion of active components due to the limited mobility of the impregnation liquid.The rotating packed bed(RPB)can break the precursor solution into fine droplets,enabling dynamic impregnation of active components onto the surface of activated carbon.This approach facilitates the uniform distribution of active components on the carrier and enhances the stability and performance of the catalyst.In this study,activated carbon catalysts were prepared using high-gravity technology.It was found that the preparation time for Co-MnO_(x)/GAC using the RPB method was reduced by 98%,the catalytic activity increased by 6.62%,and the loadings of active components increased by 13%and 17%,the catalytic activity remained stable after five cycles,with a significantly lower rate of metal dissolution.A suite of complementary analytical techniques demonstrates that Co-MnO_(x)/GAC(RPB)has higher homogeneity and dispersion.X-ray photoelectron spectroscopy(XPS)results indicate that Co(II)and Mn(IV)/Mn(III)are the primary active sites during the catalytic decomposition of ozone,elucidating the mechanism of synergistic catalytic ozonation by dual-active components.Finally,electron paramagnetic resonance(EPR)confirmed that hydroxyl radicals($OH)were the predominant reactive species in the reaction.展开更多
Molten salt reactors,being the only reactor type among Generation Ⅳ advanced nuclear reactors that utilize liquid fuels,offer inherent safety,high-temperature,and low-pressure operation,as well as the capability for ...Molten salt reactors,being the only reactor type among Generation Ⅳ advanced nuclear reactors that utilize liquid fuels,offer inherent safety,high-temperature,and low-pressure operation,as well as the capability for online fuel reprocessing.However,the fuel-salt flow results in the decay of delayed neutron precursors(DNPs)outside the core,causing fluctuations in the effective delayed neutron fraction and consequently impacting the reactor reactivity.Particularly in accident scenarios—such as a combined pump shutdown and the inability to rapidly scram the reactor—the sole reliance on negative temperature feedback may cause a significant increase in core temperature,posing a threat to reactor safety.To address these problems,this paper introduces an innovative design for a passive fluid-driven suspended control rod(SCR)to dynamically compensate for reactivity fluctuations caused by DNPs flowing with the fuel.The control rod operates passively by leveraging the combined effects of gravity,buoyancy,and fluid dynamic forces,thereby eliminating the need for an external drive mechanism and enabling direct integration within the active region of the core.Using a 150 MWt thorium-based molten salt reactor as the reference design,we develop a mathematical model to systematically analyze the effects of key parameters—including the geometric dimensions and density of the SCR—on its performance.We examine its motion characteristics under different core flow conditions and assess its feasibility for the dynamic compensation of reactivity changes caused by fuel flow.The results of this study demonstrate that the SCR can effectively counteract reactivity fluctuations induced by fuel flow within molten salt reactors.A sensitivity analysis reveals that the SCR’s average density exerts a profound impact on its start-up flow threshold,channel flow rate,resistance to fuel density fluctuations,and response characteristics.This underscores the critical need to optimize this parameter.Moreover,by judiciously selecting the SCR’s length,number of deployed units,and the placement we can achieve the necessary reactivity control while maintaining a favorable balance between neutron economy and heat transfer performance.Ultimately,this paper provides an innovative solution for the passive reactivity control in molten salt reactors,offering significant potential for practical engineering applications.展开更多
Laser-induced aerosols,predominantly submicron in size,pose significant environmental and health risks during the decommissioning of nuclear reactors.This study experimentally investigated the removal of laser-generat...Laser-induced aerosols,predominantly submicron in size,pose significant environmental and health risks during the decommissioning of nuclear reactors.This study experimentally investigated the removal of laser-generated aerosol particles using a water spray system integrated with an innovative system for pre-injecting electrically charged mist in our facility.To simulate aerosol generation in reactor decommissioning,a high-power laser was used to irradiate various materials(including stainless steel,carbon steel,and concrete),generating aerosol particles that were agglomerated with injected water mist and subsequently scavenged by water spray.Experimental results demonstrate enhanced aerosol removal via aerosol-mist agglomeration,with charged mist significantly improving particle capture by increasing wettability and size.The average improvements for the stainless steel,carbon steel,and concrete were 40%,44%,and 21%,respectively.The results of experiments using charged mist with different polarities(both positive and negative)and different surface coatings reveal that the dominant polarity of aerosols varies with the irradiated materials,influenced by their crystal structure and electron emission properties.Notably,surface coatings such as ZrO_(2)and CeO_(2)were found to possibly alter aerosol charging characteristics,thereby affecting aerosol removal efficiency with charged mist configurations.The innovative aerosol-mist agglomeration approach shows promise in mitigating radiation exposure,ensuring environmental safety,and reducing contaminated water during reactor dismantling.This study contributes critical knowledge for the development of advanced aerosol management strategies for nuclear reactor decommissioning.The understanding obtained in this work is also expected to be useful for various environmental and chemical engineering applications such as gas decontamination,air purification,and pollution control.展开更多
The photothermal pathway for converting carbon dioxide(CO_(2))into hydrocarbons presents an effective and straightforward production for solar fuels.Nonetheless,the rational design of a robust solar-driven catalytic s...The photothermal pathway for converting carbon dioxide(CO_(2))into hydrocarbons presents an effective and straightforward production for solar fuels.Nonetheless,the rational design of a robust solar-driven catalytic system for efficient CO_(2)conversion remains a persistent challenge.In this work,we elaborately construct a multi-shell Au@Rh nanoantenna reactor for photothermal CO_(2)methanation.The plasmonically active multi-shell Au structure serves as“antenna”,and the catalytically active Rh nanoparticles function as“reactor”.The reactor exhibits a superior CH_(4) yield rate and nearly 100% selectivity,in comparison with the other Au structures(single-shell(SS)and nanoparticle)and the kinds of active sites(Ru,Ir,and Co).The well-arranged Au nanoparticles in multi-shell structure provide the collective plasmon-coupled excitation,leading to the strong localized surface plasmon resonance(LSPR)effect.Then,the antenna could convert the wide-spectrum solar energy to high surface temperature and enhanced electric field.The in-situ spectra and theoretical calculation indicate that the CO_(2)methanation reaction in Au@Rh nanoantenna reactor follows the formyl pathway.The strong electron-proton coupling transfer ability of Au@Rh nanoantenna reactor contributes to the complex reaction pathway for CO_(2)methanation.Especially,compared with Au catalyst,both the formation of intermediate and the key transformation from to in Au@Rh nanoantenna reactor were promoted through the adequate supply of proton-electron pair and the strong interaction between Au and Rh sites.The ingenious design for nanoantenna reactor and the new findings in photothermal CO_(2)methanation will inspire the development of mild hydrogenation for boosting CO_(2)-to-fuel conversion.展开更多
The WC/CoCrFeNiAl0.2 high-entropy alloy(HEA)composites were prepared through high-gravity combustion synthesis.The preparation method is presented below.First,using a designed suitable multiphase thermite system,the m...The WC/CoCrFeNiAl0.2 high-entropy alloy(HEA)composites were prepared through high-gravity combustion synthesis.The preparation method is presented below.First,using a designed suitable multiphase thermite system,the molten CoCrFeNiAl0.2 HEA was fabricated using low-cost metal oxides.The molten HEA was subsequently infiltrated into the WC layer to fabricate WC/CoCrFeNiAl0.2 composites in a highgravity field.The porosity of the WC/CoCrFeNiAl0.2 composites was down-regulated,and their compressive yield strength was up-regulated when the high-gravity field was increased from 600g to 1500g because this infiltration process of a HEA melt into the WC layer is driven by centrifugal force.The WC particles in the composites exhibited a gradient distribution along the direction of the centrifugal force,which was attributed to the combined action of the high-gravity field and the temperature gradient field.The Vickers hardness of the sample was down-regulated from 9.53 to 7.41 GPa along the direction of the centrifugal force.展开更多
The degradation and mineralization of aniline （AN） using ozone combined with Fenton reagent （O3/Fenton） in a rotating packed bed （RPB） was proposed in this study, and the process （RPB-O3/Fenton） was compared w...The degradation and mineralization of aniline （AN） using ozone combined with Fenton reagent （O3/Fenton） in a rotating packed bed （RPB） was proposed in this study, and the process （RPB-O3/Fenton） was compared with conventional O3/Fenton in a stirred tank reactor （STR-O3/Fenton） or single ozonation in an RPB （RPB-O3）, Effects of high gravity factor, H2O2 dosage, H2O2 dosing method and initial pH on the AN mineralization efficiency were investigated in the RPB-O3/Fenton process, In addition, the behavior of Fe（Ⅱ） was monitored at different H2O2 dosing methods and pH values. Finally, the optimal operation conditions were determined with high gravity factor of 100, initial pH of 5, Fe（Ⅱ） concentration of 0.8 mmol·L-1 and H2O2 dosage of 2.5 ml. Under these conditions, for aniline wastewater at the volume of I L and concentration of 200 mg· L- 1 ,a fast and thorough decay of AN was conducted in 10 min, and the TOC removal efficiency reached 89% in 60 min. The main intermediates of p-benzoquinone, nitrobenzene, maleic acid and oxalic acid were identified by liquid chromatography/mass spectroscopy （LC/MS）, and the degradation pathways of AN in RPB-O3/Fenton system were proposed based on experimental evidence. It could be envisioned that high-gravity technology combined with O3/Fenton processes would be promising in the rapid and efficient mineralization ofwastewater.展开更多
The nanoparticles of the hydrophobic drug of danazol with narrow size distribution are facilely prepared by controlled high-gravity anti-solvent precipitation （HGAP） process. Intensified micromixing and uniform nucl...The nanoparticles of the hydrophobic drug of danazol with narrow size distribution are facilely prepared by controlled high-gravity anti-solvent precipitation （HGAP） process. Intensified micromixing and uniform nucleation environment are created by the high-gravity equipment （rotating packed bed） in carrying out the anti-solvent precipitation process to produce nanoparticles. The average particle size decreases from 55 μm of the raw danazol to 190 nm of the nanoparticles. The Brunauer-Emmett-Teller （BET） surface area sharply increases from 0.66 m^2·g^-1 to 15.08 m^2·g^-l. Accordingly, the dissolution rate is greatly improved. The molecular state, chemical composition, and crystal form of the danazol nanoparticles remains unchanged after processing according to Fourier transform infrared （FTIR） and X-ray diffraction （XRD）, The high recovery ratio and continuous production capacity are highly appreciated in industry. Therefore, the HGAP method might offer a general and facile platform for mass production of hydrophobic pharmaceutical danazol particles in nanometer range.展开更多
In this study,a practical process for ozonization of benzyl alcohols to ketones and aldehydes in a rotating packed bed(RPB-O3)reactor has been developed.Using 1-phenylethanol as a model reactant,the performance of RPB...In this study,a practical process for ozonization of benzyl alcohols to ketones and aldehydes in a rotating packed bed(RPB-O3)reactor has been developed.Using 1-phenylethanol as a model reactant,the performance of RPB-O3 process in different solvents has been compared with the commonly used stirred tank reactor(STR-O3).Ethyl acetate was the optimum solvent for the conversion of 1-phenylenthanol to acetophenone in RPB-O3 process,with 78%yield after 30 min.In a parallel STR-O3 experiment,the yield of acetophenone was50%.Other experimental variables,i.e.O3 concentration,reaction time,high-gravity factor and liquid flow rate were also optimized.The highest yield of acetophenone was obtained using O3 concentration of 80 mg·L-1,reaction time of 30 min,high gravity factor of 40 and liquid flow rate of 120 L·h-1.Under the optimized reaction conditions,a series of structurally diverse primary and secondary alcohols was oxidized with(19%–92%)yield.The ozonization mechanism was studied by Electron Paramagnetic Resonance(EPR)spectroscopy,monitoring the radical species formed upon self-decomposition of O3.The characteristic quadruple peak with the 1:2:2:1 intensity ratio that corresponds to hydroxyl radicals(·OH)was observed in the electron paramagnetic resonance(EPR)spectrum,indicating an indirect oxidation mechanism of alcohols via·OH radical.展开更多
The study herein investigated the effectiveness of simultaneous use of ozone and hydrogen peroxide(O_3/H_2O_2 process) to degrade o-phenylenediamine(o-PDA) in a simulated wastewater. A rotor–stator reactor(RSR) was e...The study herein investigated the effectiveness of simultaneous use of ozone and hydrogen peroxide(O_3/H_2O_2 process) to degrade o-phenylenediamine(o-PDA) in a simulated wastewater. A rotor–stator reactor(RSR) was employed to create a high-gravity environment in order to enhance ozone-liquid mass transfer rate and possibly improve the degradation rate of o-PDA. The degradation efficiency of o-PDA(η) as well as the overall gas-phase volumetric mass transfer coefficient(KGa) were determined under different operating conditions of H_2O_2 concentration, initial o-PDA concentration, temperature of reaction, initial p H and rotation speed of RSR in attempt to establish the optimal conditions. Chemical oxygen demand reduction rate(rCOD) of wastewater treated at a particular set of conditions was also analyzed. Additionally, the intermediate products of degradation were identified using a gas chromatography-mass spectrometer(GC/MS) to further evaluate the extent of o-PDA degradation as well as establish its possible degradation pathway. Results were validated by comparison with those of sole use of ozone(O_3 process), and it was noted that η, KGa and rCODachieved by O_3/H_2O_2 process was 24.4%,31.6% and 25.2% respectively higher than those of O_3 process, indicating that H_2O_2 can greatly enhance ozonation of o-PDA. This work further demonstrates that an RSR can significantly intensify ozone-liquid mass transfer rate and thus provides a feasible intensification means for the ozonation of o-PDA as well as other recalcitrant organics.展开更多
Poly(ethylene glycol)-poly(n-butyl cyanoacrylate)(PEG-PBCA)is a remarkable drug delivery carrier for permeating blood-brain barrier.In this work,a novel high-gravity procedure was reported to intensify Knoevenagel con...Poly(ethylene glycol)-poly(n-butyl cyanoacrylate)(PEG-PBCA)is a remarkable drug delivery carrier for permeating blood-brain barrier.In this work,a novel high-gravity procedure was reported to intensify Knoevenagel condensation-Michael addition polymerization of PEG-PBCA.A series of PEG-PBCA containing different block ratios were synthesized with narrow molecular weight distribution of polydispersity indexes less than 1.1.Furthermore,the reaction time reduced 60%compared to conventional stirred tank reactor process.Chemical structures of as-prepared polymers were characterized.In vitro drug delivery performance was evaluated.The cytotoxicity of PEG-PBCA to brain microvessel endothelial cells(BMVEC)decreases with the extension of the PEG chain and the shortening of the PBCA chain.The polymer cellular uptake to BMVECs was better after improving hydrophilicity by PEG block.Results of bloodbrain barrier permeability demonstrated that medium length of PBCA chain and short PEG chain are favorable for hydrophobic Nile red permeation,while long PEG chain and short PBCA chain are beneficial to delivery water-soluble doxorubicin hydrochloride(Dox).The average apparent permeability coeffi-cient increased 1.7 and 0.25 times than that of raw Nile red and Dox,respectively.High-gravity intensi-fied condensation polymerization should have great potential in brain drug delivery system.展开更多
In this study,high-gravity intensified heterogeneous catalytic ozonation is utilized for treatment of phenol-containing wastewater,and the kinetics of the direct reaction between ozone and phenol in the presence of ex...In this study,high-gravity intensified heterogeneous catalytic ozonation is utilized for treatment of phenol-containing wastewater,and the kinetics of the direct reaction between ozone and phenol in the presence of excess tertiary butanol(TBA)is investigated.It is revealed that the direct reaction between ozone and phenol in the rotating packed bed(RPB)follows the pseudo-first-order kinetics with a reaction rate constant higher than that in the conventional bubbling reactor(BR).Under different conditions of temperature,initial pH,high-gravity factor,and gaseous ozone concentration,the apparent reaction rate constant varies in the range of 0.0160–0.115 min-1.An empirical power-exponential model is established to characterize the effects of these parameters on the direct reaction between ozone and phenol by high-gravity intensified heterogeneous catalytic ozonation.展开更多
In this study,an integrated technology is proposed for the absorption and utilization of CO_(2)in alkanolamine solution for the preparation of BaCO_(3)in a high-gravity environment.The effects of absorbent type,high-g...In this study,an integrated technology is proposed for the absorption and utilization of CO_(2)in alkanolamine solution for the preparation of BaCO_(3)in a high-gravity environment.The effects of absorbent type,high-gravity factor,gas/liquid ratio,and initial BaCl2concentration on the absorption rate and amount of CO_(2)and the preparation of BaCO_(3)are investigated.The results reveal that the absorption rate and amount of CO_(2)follow the order of ethyl alkanolamine(MEA)>diethanol amine(DEA)>N-methyldiethanolamine(MDEA),and thus MEA is the most effective absorbent for CO_(2)absorption.The absorption rate and amount of CO_(2)under high gravity are higher than that under normal gravity.Notably,the absorption rate at 75 min under high gravity is approximately 2 times that under normal gravity.This is because the centrifugal force resulting from the high-speed rotation of the packing can greatly increase gas-liquid mass transfer and micromixing.The particle size of BaCO_(3)prepared in the rotating packed bed is in the range of 57.2—89 nm,which is much smaller than that prepared in the bubbling reactor(>100.3 nm),and it also has higher purity(99.6%)and larger specific surface area(14.119 m^(2)·g^(-1)).It is concluded that the high-gravity technology has the potential to increase the absorption and utilization of CO_(2)in alkanolamine solution for the preparation of BaCO_(3).This study provides new insights into carbon emissions reduction and carbon utilization.展开更多
AbstFeS has an excellent performance in removing heavy metal chromium(Ⅵ)in wastewater due to its good adsorption and reduction.The properties of easy aggregation and oxidization of nano-FeS,however,limit the applicat...AbstFeS has an excellent performance in removing heavy metal chromium(Ⅵ)in wastewater due to its good adsorption and reduction.The properties of easy aggregation and oxidization of nano-FeS,however,limit the applications of FeS in engineering.In this study,one FeS adsorbent supported by Al_(2)O_(3) was prepared using high-gravity technology in IS-RPB(Impinging Stream Rotating Packed Bed)to overcome polymerization and oxidation of nano-FeS.Experimental results showed that FeS was uniformly loaded on the surface and pores of Al_(2)O_(3).The specific surface area of FeS/Al_(2)O_(3) is 125 m2·g^(-1) which is nearly 1.6 times that of pure FeS.The adsorption capacity of FeS/Al_(2)O_(3) for chromium(Ⅵ)is 200 mg·g^(-1),1.4 times that of pure FeS.pH value and ionic strength are strongly correlated with the chromium removal performance of FeS/Al_(2)O_(3).Over 98%of chromium can be removed when pH values of FeS/Al_(2)O_(3) ranged from 4 to 6.Higher adsorption capacity is achieved with higher ionic strength in FeS/Al_(2)O_(3).The FeS/Al_(2)O_(3) maintained more than 95%of the adsorption capacity after being preserved for one month,but only 70%for pure FeS.The removal processes of chromium(Ⅵ)conformes to a pseudo-second-order kinetic model(R2≥0.9986),indicating that the rate-limiting step is a chemical sorption process instead of a mass transfer.展开更多
Small modular reactor(SMR)belongs to the research forefront of nuclear reactor technology.Nowadays,advancement of intelligent control technologies paves a new way to the design and build of unmanned SMR.The autonomous...Small modular reactor(SMR)belongs to the research forefront of nuclear reactor technology.Nowadays,advancement of intelligent control technologies paves a new way to the design and build of unmanned SMR.The autonomous control process of SMR can be divided into three stages,say,state diagnosis,autonomous decision-making and coordinated control.In this paper,the autonomous state recognition and task planning of unmanned SMR are investigated.An operating condition recognition method based on the knowledge base of SMR operation is proposed by using the artificial neural network(ANN)technology,which constructs a basis for the state judgment of intelligent reactor control path planning.An improved reinforcement learning path planning algorithm is utilized to implement the path transfer decision-makingThis algorithm performs condition transitions with minimal cost under specified modes.In summary,the full range control path intelligent decision-planning technology of SMR is realized,thus provides some theoretical basis for the design and build of unmanned SMR in the future.展开更多
Core power is a key parameter of nuclear reactor.Traditionally,the proportional-integralderivative(PID)controllers are used to control the core power.Fractional-order PID(FOPID)controller represents the cutting edge i...Core power is a key parameter of nuclear reactor.Traditionally,the proportional-integralderivative(PID)controllers are used to control the core power.Fractional-order PID(FOPID)controller represents the cutting edge in core power control research.In comparing with the integer-order models,fractional-order models describe the variation of core power more accurately,thus provide a comprehensive and realistic depiction for the power and state changes of reactor core.However,current fractional-order controllers cannot adjust their parameters dynamically to response the environmental changes or demands.In this paper,we aim at the stable control and dynamic responsiveness of core power.Based on the strong selflearning ability of artificial neural network(ANN),we propose a composite controller combining the ANN and FOPID controller.The FOPID controller is firstly designed and a back propagation neural network(BPNN)is then utilized to optimize the parameters of FOPID.It is shown by simulation that the composite controller enables the real-time parameter tuning via ANN and retains the advantage of FOPID controller.展开更多
A radical C−C-coupling reaction of acetonitrile into succinonitrile over hydrophobic TiO_(2) photocatalyst with enhanced catalytic activity was developed.In addition,the usage of a flow reactor further improved the ph...A radical C−C-coupling reaction of acetonitrile into succinonitrile over hydrophobic TiO_(2) photocatalyst with enhanced catalytic activity was developed.In addition,the usage of a flow reactor further improved the photon utilization efficiency for succinonitrile synthesis at room temperature.The space time yield of succinonitrile reached 55.59μmol/(g·h)over hydrophobic TiO_(2) catalyst,which was much higher than that of pristine TiO_(2)(4.23μmol/(g·h)).Mechanistic studies revealed that the hydrophobic modification of TiO_(2) promoted the separation and transfer of photogenerated carriers,as well as suppressed their recombination.Hydrophobic TiO_(2) also enhanced the adsorption of−CH3 of acetonitrile,thus facilitating the activation of C−H bond and the utilization efficiency of photocarriers.展开更多
Based on the service characteristics of fuel elements for molten salt reactors,they need to have a high power density,resistance to coolant infiltration,and excellent thermodynamic properties.To solve the problem of t...Based on the service characteristics of fuel elements for molten salt reactors,they need to have a high power density,resistance to coolant infiltration,and excellent thermodynamic properties.To solve the problem of the graphite used in the fuel element for these reactors being susceptible to molten salt infiltration,carbon black(CB)was added to increase the density of the graphite,and a fuel element(TRISO(tri-structural isotropic)fuel particles were randomly distributed in the modified graphite matrix)was prepared by cold isostatic pressing process.An out-of-pile performance study shows that the densification and pore structure of the modified graphite matrix were improved,as was the resistance to molten salt infiltration.The median pore size of the modified graphite was reduced from 673 to 433 nm and the threshold pressure for molten salt(FLiBe,66%(molar fraction)LiF and 34%BeF_(2))infiltration was increased from 0.88 to 1.37 MPa.The isotropic CB made the graphite matrix less anisotropic,while its thermal conductivity and compressive strength were reduced due to the difficult graphitization of CB.Fuel elements containing 20%(volume fraction)TRISO particles were prepared.Numerical simulations show that the power and temperature distribution of the fuel were in line with the design requirements.The modified graphite matrix had a higher density,smaller pores,a lower anisotropy and a greater resistance to FLiBe infiltration.展开更多
Electrocatalytic carbon dioxide reduction is a promising technology for addressing global energy and environmental crises. However, its practical application faces two critical challenges: the complex and energy-inten...Electrocatalytic carbon dioxide reduction is a promising technology for addressing global energy and environmental crises. However, its practical application faces two critical challenges: the complex and energy-intensive process of separat-ing mixed reduction products and the economic viability of the carbon sources (reactants) used. To tackle these challenges simultaneously, solid-state electrolyte (SSE) reactors are emerging as a promising solution. In this review, we focus on the feasibility of applying SSE for tandem electrochemical CO_(2) capture and conversion. The configurations and fundamental principles of SSE reactors are first discussed, followed by an introduction to its applications in these two specific areas, along with case studies on the implementation of tandem electrolysis. In comparison to conventional H-type cell, flow cell and membrane electrode assembly cell reactors, SSE reactors incorporate gas diffusion electrodes and utilize a solid electro-lyte layer positioned between an anion exchange membrane (AEM) and a cation exchange membrane (CEM). A key inno-vation of this design is the sandwiched SSE layer, which enhances efficient ion transport and facilitates continuous product extraction through a stream of deionized water or humidified nitrogen, effectively separating ion conduction from product collection. During electrolysis, driven by an electric field and concentration gradient, electrochemically generated ions (e.g., HCOO- and CH3COO-) migrate through the AEM into the SSE layer, while protons produced from water oxidation at the anode traverse the CEM into the central chamber to maintain charge balance. Targeted products like HCOOH can form in the middle layer through ionic recombination and are efficiently carried away by the flowing medium through the porous SSE layer, in the absence of electrolyte salt impurities. As CO_(2)RR can generate a series of liquid products, advancements in catalyst discovery over the past several years have facilitated the industrial application of SSE for more efficient chemicals production. Also noteworthy, the cathode reduction reaction can readily consume protons from water, creating a highly al-kaline local environment. SSE reactors are thereby employed to capture acidic CO_(2), forming CO_(3)^(2-) from various gas sources including flue gases. Driven by the electric field, the formed CO_(3)^(2-) can traverse through the AEM and react with protons originating from the anode, thereby regenerating CO_(2). This CO_(2) can then be collected and utilized as a low-cost feedstock for downstream CO_(2) electrolysis. Based on this principle, several cell configurations have been proposed to enhance CO_(2) capture from diverse gas sources. Through the collaboration of two SSE units, tandem electrochemical CO_(2) capture and con-version has been successfully implemented. Finally, we offer insights into the future development of SSE reactors for prac-tical applications aimed at achieving carbon neutrality. We recommend that greater attention be focused on specific aspects, including the fundamental physicochemical properties of the SSE layer, the electrochemical engineering perspective related to ion and species fluxes and selectivity, and the systematic pairing of consecutive CO_(2) capture and conversion units. These efforts aim to further enhance the practical application of SSE reactors within the broader electrochemistry community.展开更多
Liquid-fueled molten-salt reactors have dynamic features that distinguish them from solid-fueled reactors,such that conventional system-analysis codes are not directly applicable.In this study,a coupled dynamic model ...Liquid-fueled molten-salt reactors have dynamic features that distinguish them from solid-fueled reactors,such that conventional system-analysis codes are not directly applicable.In this study,a coupled dynamic model of the Molten-Salt Reactor Experiment(MSRE)is developed.The coupled model includes the neutronics and single-phase thermal-hydraulics modeling of the reactor and validated xenon-transport modeling from previous studies.The coupled dynamic model is validated against the frequency-response and transient-response data from the MSRE.The validated model is then applied to study the effects of xenon and void transport on the dynamic behaviors of the reactor.Plant responses during the unique initiating events such as off-gas system blockages and loss of circulating voids are investigated.展开更多
基金The financial support from the Nature Scientific Foundation of Heilongjiang Province(No.YQ2022E041)the Postdoctoral Research Start-up Funds in Heilongjiang Province(No.2023BSH14)the Basic scientific research project of Heilongjiang Provincial University(No.2024-KYYWF-1090)。
文摘Hydrate-based gas separation offers a promising approach for coalbed methane recovery,reaching energy conservation and emissions reduction.This study innovatively applied high-gravity technology to enhance hydrate formation in separating 25%CH_(4)/67%N_(2)/8%O_(2) for achieving rapid and efficient methane recovery.Systematic investigations were conducted at 283.2 K and 3.0 MPa with tetrahydrofuran at a molar concentration of 5.56%and L-tryptophan at a mass concentration of 0.5%additives,first evaluating liquid flow rate effects(0–20 mL/min)on mixed hydrate kinetic performance and separation efficiency,followed by rotating speed optimization(0–1200 r·min^(-1))under the optimal liquid flow rate.The high-gravity system amplified the gas–liquid contact area by~1155 times through cascaded liquid supply and secondary shear effects,methane molecules entered the hydrate phase rapidly under the highest driving force with the significantly intensified mass transfer.Optimal conditions(20 mL/min,600 r·min^(-1))yielded an exceptional initial hydrate growth rate of 58.59 mmol/(mol·h)and methane recovery of 50.76%,about 71.33 and 0.58 times higher than the static system,respectively.Gas chromatography and Raman spectrometer analyses revealed superior methane enrichment in hydrate phase at 90%gas uptake completion,with a concurrent 41.17%reduction in process duration.These findings demonstrate the efficacy of high-gravity-enhanced hydrate technology for coalbed methane separation,offering valuable insights for optimizing clean energy utilization.
基金supported by the National Natural Science Foundation of China(U23A20676)Key Research&Development Plan of Shanxi Province(202202040201011)+3 种基金Shanxi Scholarship Council of China(2023-128)Small and medium-sized oriented scientific and technological enterprises innovation ability improvement project of Shandong Province(2023TSGC0004)the Graduate Student Innovation Project of Shanxi Province(2023SJ205)Local Funds for Science and Technology Development Guided by the Central Finance(YDZJSX20231A030).
文摘The impregnation method for preparing catalysts often faces challenges such as prolonged preparation times and poor dispersion of active components due to the limited mobility of the impregnation liquid.The rotating packed bed(RPB)can break the precursor solution into fine droplets,enabling dynamic impregnation of active components onto the surface of activated carbon.This approach facilitates the uniform distribution of active components on the carrier and enhances the stability and performance of the catalyst.In this study,activated carbon catalysts were prepared using high-gravity technology.It was found that the preparation time for Co-MnO_(x)/GAC using the RPB method was reduced by 98%,the catalytic activity increased by 6.62%,and the loadings of active components increased by 13%and 17%,the catalytic activity remained stable after five cycles,with a significantly lower rate of metal dissolution.A suite of complementary analytical techniques demonstrates that Co-MnO_(x)/GAC(RPB)has higher homogeneity and dispersion.X-ray photoelectron spectroscopy(XPS)results indicate that Co(II)and Mn(IV)/Mn(III)are the primary active sites during the catalytic decomposition of ozone,elucidating the mechanism of synergistic catalytic ozonation by dual-active components.Finally,electron paramagnetic resonance(EPR)confirmed that hydroxyl radicals($OH)were the predominant reactive species in the reaction.
基金supported by Youth Innovation Promotion Association of Chinese Academy of Sciences(No.2020261)Strategic Priority Research Program of Chinese Academy of Sciences(No.XDA02010000)the Young Potential Program of Shanghai Institute of Applied Physics,Chinese Academy of Sciences(No.SINAP-YXJH-202412).
文摘Molten salt reactors,being the only reactor type among Generation Ⅳ advanced nuclear reactors that utilize liquid fuels,offer inherent safety,high-temperature,and low-pressure operation,as well as the capability for online fuel reprocessing.However,the fuel-salt flow results in the decay of delayed neutron precursors(DNPs)outside the core,causing fluctuations in the effective delayed neutron fraction and consequently impacting the reactor reactivity.Particularly in accident scenarios—such as a combined pump shutdown and the inability to rapidly scram the reactor—the sole reliance on negative temperature feedback may cause a significant increase in core temperature,posing a threat to reactor safety.To address these problems,this paper introduces an innovative design for a passive fluid-driven suspended control rod(SCR)to dynamically compensate for reactivity fluctuations caused by DNPs flowing with the fuel.The control rod operates passively by leveraging the combined effects of gravity,buoyancy,and fluid dynamic forces,thereby eliminating the need for an external drive mechanism and enabling direct integration within the active region of the core.Using a 150 MWt thorium-based molten salt reactor as the reference design,we develop a mathematical model to systematically analyze the effects of key parameters—including the geometric dimensions and density of the SCR—on its performance.We examine its motion characteristics under different core flow conditions and assess its feasibility for the dynamic compensation of reactivity changes caused by fuel flow.The results of this study demonstrate that the SCR can effectively counteract reactivity fluctuations induced by fuel flow within molten salt reactors.A sensitivity analysis reveals that the SCR’s average density exerts a profound impact on its start-up flow threshold,channel flow rate,resistance to fuel density fluctuations,and response characteristics.This underscores the critical need to optimize this parameter.Moreover,by judiciously selecting the SCR’s length,number of deployed units,and the placement we can achieve the necessary reactivity control while maintaining a favorable balance between neutron economy and heat transfer performance.Ultimately,this paper provides an innovative solution for the passive reactivity control in molten salt reactors,offering significant potential for practical engineering applications.
基金financial support from the Nuclear Energy Science&Technology and Human Resource Development Project of the Japan Atomic Energy Agency/Collaborative Laboratories for Advanced Decommissioning Science(No.R04I034)The author Ruicong Xu appreciates the scholarship(financial support)from the China Scholarship Council(CSC,No.202106380073).
文摘Laser-induced aerosols,predominantly submicron in size,pose significant environmental and health risks during the decommissioning of nuclear reactors.This study experimentally investigated the removal of laser-generated aerosol particles using a water spray system integrated with an innovative system for pre-injecting electrically charged mist in our facility.To simulate aerosol generation in reactor decommissioning,a high-power laser was used to irradiate various materials(including stainless steel,carbon steel,and concrete),generating aerosol particles that were agglomerated with injected water mist and subsequently scavenged by water spray.Experimental results demonstrate enhanced aerosol removal via aerosol-mist agglomeration,with charged mist significantly improving particle capture by increasing wettability and size.The average improvements for the stainless steel,carbon steel,and concrete were 40%,44%,and 21%,respectively.The results of experiments using charged mist with different polarities(both positive and negative)and different surface coatings reveal that the dominant polarity of aerosols varies with the irradiated materials,influenced by their crystal structure and electron emission properties.Notably,surface coatings such as ZrO_(2)and CeO_(2)were found to possibly alter aerosol charging characteristics,thereby affecting aerosol removal efficiency with charged mist configurations.The innovative aerosol-mist agglomeration approach shows promise in mitigating radiation exposure,ensuring environmental safety,and reducing contaminated water during reactor dismantling.This study contributes critical knowledge for the development of advanced aerosol management strategies for nuclear reactor decommissioning.The understanding obtained in this work is also expected to be useful for various environmental and chemical engineering applications such as gas decontamination,air purification,and pollution control.
基金supported by the National Natural Science Foundation of China(Nos.92477134 and 52572007)the National Key Research and Development Program of China(No.2023YFB3507700)+1 种基金the Taishan Scholar Project of Shandong Province(No.tsqn202408205)Provincial Natural Science Foundation of Shandong(No.ZR2023ME014).
文摘The photothermal pathway for converting carbon dioxide(CO_(2))into hydrocarbons presents an effective and straightforward production for solar fuels.Nonetheless,the rational design of a robust solar-driven catalytic system for efficient CO_(2)conversion remains a persistent challenge.In this work,we elaborately construct a multi-shell Au@Rh nanoantenna reactor for photothermal CO_(2)methanation.The plasmonically active multi-shell Au structure serves as“antenna”,and the catalytically active Rh nanoparticles function as“reactor”.The reactor exhibits a superior CH_(4) yield rate and nearly 100% selectivity,in comparison with the other Au structures(single-shell(SS)and nanoparticle)and the kinds of active sites(Ru,Ir,and Co).The well-arranged Au nanoparticles in multi-shell structure provide the collective plasmon-coupled excitation,leading to the strong localized surface plasmon resonance(LSPR)effect.Then,the antenna could convert the wide-spectrum solar energy to high surface temperature and enhanced electric field.The in-situ spectra and theoretical calculation indicate that the CO_(2)methanation reaction in Au@Rh nanoantenna reactor follows the formyl pathway.The strong electron-proton coupling transfer ability of Au@Rh nanoantenna reactor contributes to the complex reaction pathway for CO_(2)methanation.Especially,compared with Au catalyst,both the formation of intermediate and the key transformation from to in Au@Rh nanoantenna reactor were promoted through the adequate supply of proton-electron pair and the strong interaction between Au and Rh sites.The ingenious design for nanoantenna reactor and the new findings in photothermal CO_(2)methanation will inspire the development of mild hydrogenation for boosting CO_(2)-to-fuel conversion.
基金financially supported by the National Key R&D Program of China (No. 2017YFB0310303)the National Natural Science Foundation of China (No. 51702332)the Key Laboratory of Cryogenics, TIPC, CAS (Nos. CRYOQN201705 and CRYOQN201507)
文摘The WC/CoCrFeNiAl0.2 high-entropy alloy(HEA)composites were prepared through high-gravity combustion synthesis.The preparation method is presented below.First,using a designed suitable multiphase thermite system,the molten CoCrFeNiAl0.2 HEA was fabricated using low-cost metal oxides.The molten HEA was subsequently infiltrated into the WC layer to fabricate WC/CoCrFeNiAl0.2 composites in a highgravity field.The porosity of the WC/CoCrFeNiAl0.2 composites was down-regulated,and their compressive yield strength was up-regulated when the high-gravity field was increased from 600g to 1500g because this infiltration process of a HEA melt into the WC layer is driven by centrifugal force.The WC particles in the composites exhibited a gradient distribution along the direction of the centrifugal force,which was attributed to the combined action of the high-gravity field and the temperature gradient field.The Vickers hardness of the sample was down-regulated from 9.53 to 7.41 GPa along the direction of the centrifugal force.
基金Supported by the National Natural Science Foundations of China(U1610106)Shanxi Excellent Talent Science and Technology Innovation Project(201705D211011)+1 种基金Specialized Research Fund for Sanjin Scholars Program of Shanxi ProvinceNorth University of China Fund for Distinguished Young Scholars
文摘The degradation and mineralization of aniline （AN） using ozone combined with Fenton reagent （O3/Fenton） in a rotating packed bed （RPB） was proposed in this study, and the process （RPB-O3/Fenton） was compared with conventional O3/Fenton in a stirred tank reactor （STR-O3/Fenton） or single ozonation in an RPB （RPB-O3）, Effects of high gravity factor, H2O2 dosage, H2O2 dosing method and initial pH on the AN mineralization efficiency were investigated in the RPB-O3/Fenton process, In addition, the behavior of Fe（Ⅱ） was monitored at different H2O2 dosing methods and pH values. Finally, the optimal operation conditions were determined with high gravity factor of 100, initial pH of 5, Fe（Ⅱ） concentration of 0.8 mmol·L-1 and H2O2 dosage of 2.5 ml. Under these conditions, for aniline wastewater at the volume of I L and concentration of 200 mg· L- 1 ,a fast and thorough decay of AN was conducted in 10 min, and the TOC removal efficiency reached 89% in 60 min. The main intermediates of p-benzoquinone, nitrobenzene, maleic acid and oxalic acid were identified by liquid chromatography/mass spectroscopy （LC/MS）, and the degradation pathways of AN in RPB-O3/Fenton system were proposed based on experimental evidence. It could be envisioned that high-gravity technology combined with O3/Fenton processes would be promising in the rapid and efficient mineralization ofwastewater.
基金Supported by the National High Technology Research and Development Program of China (2006AA030202)the Talent Training Program of Beijing (2007B022)
文摘The nanoparticles of the hydrophobic drug of danazol with narrow size distribution are facilely prepared by controlled high-gravity anti-solvent precipitation （HGAP） process. Intensified micromixing and uniform nucleation environment are created by the high-gravity equipment （rotating packed bed） in carrying out the anti-solvent precipitation process to produce nanoparticles. The average particle size decreases from 55 μm of the raw danazol to 190 nm of the nanoparticles. The Brunauer-Emmett-Teller （BET） surface area sharply increases from 0.66 m^2·g^-1 to 15.08 m^2·g^-l. Accordingly, the dissolution rate is greatly improved. The molecular state, chemical composition, and crystal form of the danazol nanoparticles remains unchanged after processing according to Fourier transform infrared （FTIR） and X-ray diffraction （XRD）, The high recovery ratio and continuous production capacity are highly appreciated in industry. Therefore, the HGAP method might offer a general and facile platform for mass production of hydrophobic pharmaceutical danazol particles in nanometer range.
基金supported by the Specialized Research Fund for Sanjin Scholars Program of Shanxi Province(201707)Key Research&Development Plan of Shanxi Province(201903D321059)+1 种基金Shanxi Scholarship Council of China(2019032)Shanxi Graduate Education Innovation Project(2019BY106)。
文摘In this study,a practical process for ozonization of benzyl alcohols to ketones and aldehydes in a rotating packed bed(RPB-O3)reactor has been developed.Using 1-phenylethanol as a model reactant,the performance of RPB-O3 process in different solvents has been compared with the commonly used stirred tank reactor(STR-O3).Ethyl acetate was the optimum solvent for the conversion of 1-phenylenthanol to acetophenone in RPB-O3 process,with 78%yield after 30 min.In a parallel STR-O3 experiment,the yield of acetophenone was50%.Other experimental variables,i.e.O3 concentration,reaction time,high-gravity factor and liquid flow rate were also optimized.The highest yield of acetophenone was obtained using O3 concentration of 80 mg·L-1,reaction time of 30 min,high gravity factor of 40 and liquid flow rate of 120 L·h-1.Under the optimized reaction conditions,a series of structurally diverse primary and secondary alcohols was oxidized with(19%–92%)yield.The ozonization mechanism was studied by Electron Paramagnetic Resonance(EPR)spectroscopy,monitoring the radical species formed upon self-decomposition of O3.The characteristic quadruple peak with the 1:2:2:1 intensity ratio that corresponds to hydroxyl radicals(·OH)was observed in the electron paramagnetic resonance(EPR)spectrum,indicating an indirect oxidation mechanism of alcohols via·OH radical.
基金Supported by the National Natural Science Foundation of China(21276013,21676008)Specialized Research Fund for the Doctoral Program of Higher Education of China(20130010110001)
文摘The study herein investigated the effectiveness of simultaneous use of ozone and hydrogen peroxide(O_3/H_2O_2 process) to degrade o-phenylenediamine(o-PDA) in a simulated wastewater. A rotor–stator reactor(RSR) was employed to create a high-gravity environment in order to enhance ozone-liquid mass transfer rate and possibly improve the degradation rate of o-PDA. The degradation efficiency of o-PDA(η) as well as the overall gas-phase volumetric mass transfer coefficient(KGa) were determined under different operating conditions of H_2O_2 concentration, initial o-PDA concentration, temperature of reaction, initial p H and rotation speed of RSR in attempt to establish the optimal conditions. Chemical oxygen demand reduction rate(rCOD) of wastewater treated at a particular set of conditions was also analyzed. Additionally, the intermediate products of degradation were identified using a gas chromatography-mass spectrometer(GC/MS) to further evaluate the extent of o-PDA degradation as well as establish its possible degradation pathway. Results were validated by comparison with those of sole use of ozone(O_3 process), and it was noted that η, KGa and rCODachieved by O_3/H_2O_2 process was 24.4%,31.6% and 25.2% respectively higher than those of O_3 process, indicating that H_2O_2 can greatly enhance ozonation of o-PDA. This work further demonstrates that an RSR can significantly intensify ozone-liquid mass transfer rate and thus provides a feasible intensification means for the ozonation of o-PDA as well as other recalcitrant organics.
基金This work was supported by National Key Research and Development Program of China(2016YFA0201701).
文摘Poly(ethylene glycol)-poly(n-butyl cyanoacrylate)(PEG-PBCA)is a remarkable drug delivery carrier for permeating blood-brain barrier.In this work,a novel high-gravity procedure was reported to intensify Knoevenagel condensation-Michael addition polymerization of PEG-PBCA.A series of PEG-PBCA containing different block ratios were synthesized with narrow molecular weight distribution of polydispersity indexes less than 1.1.Furthermore,the reaction time reduced 60%compared to conventional stirred tank reactor process.Chemical structures of as-prepared polymers were characterized.In vitro drug delivery performance was evaluated.The cytotoxicity of PEG-PBCA to brain microvessel endothelial cells(BMVEC)decreases with the extension of the PEG chain and the shortening of the PBCA chain.The polymer cellular uptake to BMVECs was better after improving hydrophilicity by PEG block.Results of bloodbrain barrier permeability demonstrated that medium length of PBCA chain and short PEG chain are favorable for hydrophobic Nile red permeation,while long PEG chain and short PBCA chain are beneficial to delivery water-soluble doxorubicin hydrochloride(Dox).The average apparent permeability coeffi-cient increased 1.7 and 0.25 times than that of raw Nile red and Dox,respectively.High-gravity intensi-fied condensation polymerization should have great potential in brain drug delivery system.
基金supported by the Fund for Shanxi Province Higher Education“1331 Project”for Improving Quality and Efficiency Construction(nuc2021-006)Key Research&Development Plan of Shanxi Province(201903D321059)+1 种基金Scientific Activities of Selected Returned Overseas Professionals in Shanxi Province(20200004)Transformation and Cultivation Projects of Scientific and Technological Achievements in Universities of Shanxi Province Institutions(2020CG040).
文摘In this study,high-gravity intensified heterogeneous catalytic ozonation is utilized for treatment of phenol-containing wastewater,and the kinetics of the direct reaction between ozone and phenol in the presence of excess tertiary butanol(TBA)is investigated.It is revealed that the direct reaction between ozone and phenol in the rotating packed bed(RPB)follows the pseudo-first-order kinetics with a reaction rate constant higher than that in the conventional bubbling reactor(BR).Under different conditions of temperature,initial pH,high-gravity factor,and gaseous ozone concentration,the apparent reaction rate constant varies in the range of 0.0160–0.115 min-1.An empirical power-exponential model is established to characterize the effects of these parameters on the direct reaction between ozone and phenol by high-gravity intensified heterogeneous catalytic ozonation.
基金supported by Research Project Supported by Horizon Europe Framework Programme(101183092)Shanxi Scholarship Council of China(2023-128)+2 种基金National Natural Science Foundation of China(22208328)Fundamental Research Program of Shanxi Province(20210302124618)Small and mediumsized oriented scientific and technological enterprises innovation ability improvement project of Shandong Province(2023TSGC0004)。
文摘In this study,an integrated technology is proposed for the absorption and utilization of CO_(2)in alkanolamine solution for the preparation of BaCO_(3)in a high-gravity environment.The effects of absorbent type,high-gravity factor,gas/liquid ratio,and initial BaCl2concentration on the absorption rate and amount of CO_(2)and the preparation of BaCO_(3)are investigated.The results reveal that the absorption rate and amount of CO_(2)follow the order of ethyl alkanolamine(MEA)>diethanol amine(DEA)>N-methyldiethanolamine(MDEA),and thus MEA is the most effective absorbent for CO_(2)absorption.The absorption rate and amount of CO_(2)under high gravity are higher than that under normal gravity.Notably,the absorption rate at 75 min under high gravity is approximately 2 times that under normal gravity.This is because the centrifugal force resulting from the high-speed rotation of the packing can greatly increase gas-liquid mass transfer and micromixing.The particle size of BaCO_(3)prepared in the rotating packed bed is in the range of 57.2—89 nm,which is much smaller than that prepared in the bubbling reactor(>100.3 nm),and it also has higher purity(99.6%)and larger specific surface area(14.119 m^(2)·g^(-1)).It is concluded that the high-gravity technology has the potential to increase the absorption and utilization of CO_(2)in alkanolamine solution for the preparation of BaCO_(3).This study provides new insights into carbon emissions reduction and carbon utilization.
基金The present research was under the financial support of Shanxi Provincial Natural Fund(201901D111136).
文摘AbstFeS has an excellent performance in removing heavy metal chromium(Ⅵ)in wastewater due to its good adsorption and reduction.The properties of easy aggregation and oxidization of nano-FeS,however,limit the applications of FeS in engineering.In this study,one FeS adsorbent supported by Al_(2)O_(3) was prepared using high-gravity technology in IS-RPB(Impinging Stream Rotating Packed Bed)to overcome polymerization and oxidation of nano-FeS.Experimental results showed that FeS was uniformly loaded on the surface and pores of Al_(2)O_(3).The specific surface area of FeS/Al_(2)O_(3) is 125 m2·g^(-1) which is nearly 1.6 times that of pure FeS.The adsorption capacity of FeS/Al_(2)O_(3) for chromium(Ⅵ)is 200 mg·g^(-1),1.4 times that of pure FeS.pH value and ionic strength are strongly correlated with the chromium removal performance of FeS/Al_(2)O_(3).Over 98%of chromium can be removed when pH values of FeS/Al_(2)O_(3) ranged from 4 to 6.Higher adsorption capacity is achieved with higher ionic strength in FeS/Al_(2)O_(3).The FeS/Al_(2)O_(3) maintained more than 95%of the adsorption capacity after being preserved for one month,but only 70%for pure FeS.The removal processes of chromium(Ⅵ)conformes to a pseudo-second-order kinetic model(R2≥0.9986),indicating that the rate-limiting step is a chemical sorption process instead of a mass transfer.
文摘Small modular reactor(SMR)belongs to the research forefront of nuclear reactor technology.Nowadays,advancement of intelligent control technologies paves a new way to the design and build of unmanned SMR.The autonomous control process of SMR can be divided into three stages,say,state diagnosis,autonomous decision-making and coordinated control.In this paper,the autonomous state recognition and task planning of unmanned SMR are investigated.An operating condition recognition method based on the knowledge base of SMR operation is proposed by using the artificial neural network(ANN)technology,which constructs a basis for the state judgment of intelligent reactor control path planning.An improved reinforcement learning path planning algorithm is utilized to implement the path transfer decision-makingThis algorithm performs condition transitions with minimal cost under specified modes.In summary,the full range control path intelligent decision-planning technology of SMR is realized,thus provides some theoretical basis for the design and build of unmanned SMR in the future.
文摘Core power is a key parameter of nuclear reactor.Traditionally,the proportional-integralderivative(PID)controllers are used to control the core power.Fractional-order PID(FOPID)controller represents the cutting edge in core power control research.In comparing with the integer-order models,fractional-order models describe the variation of core power more accurately,thus provide a comprehensive and realistic depiction for the power and state changes of reactor core.However,current fractional-order controllers cannot adjust their parameters dynamically to response the environmental changes or demands.In this paper,we aim at the stable control and dynamic responsiveness of core power.Based on the strong selflearning ability of artificial neural network(ANN),we propose a composite controller combining the ANN and FOPID controller.The FOPID controller is firstly designed and a back propagation neural network(BPNN)is then utilized to optimize the parameters of FOPID.It is shown by simulation that the composite controller enables the real-time parameter tuning via ANN and retains the advantage of FOPID controller.
基金supported by the National Key R&D Program of China(2021YFF0500703)Natural Science Foundation of Shanghai(22JC1404200)+3 种基金Program of Shanghai Academic/Technology Research Leader(20XD1404000)Natural Science Foundation of China(U22B20136,22293023)Science and Technology Major Project of Inner Mongolia(2021ZD0042)the Youth Innovation Promotion Association of CAS。
文摘A radical C−C-coupling reaction of acetonitrile into succinonitrile over hydrophobic TiO_(2) photocatalyst with enhanced catalytic activity was developed.In addition,the usage of a flow reactor further improved the photon utilization efficiency for succinonitrile synthesis at room temperature.The space time yield of succinonitrile reached 55.59μmol/(g·h)over hydrophobic TiO_(2) catalyst,which was much higher than that of pristine TiO_(2)(4.23μmol/(g·h)).Mechanistic studies revealed that the hydrophobic modification of TiO_(2) promoted the separation and transfer of photogenerated carriers,as well as suppressed their recombination.Hydrophobic TiO_(2) also enhanced the adsorption of−CH3 of acetonitrile,thus facilitating the activation of C−H bond and the utilization efficiency of photocarriers.
文摘Based on the service characteristics of fuel elements for molten salt reactors,they need to have a high power density,resistance to coolant infiltration,and excellent thermodynamic properties.To solve the problem of the graphite used in the fuel element for these reactors being susceptible to molten salt infiltration,carbon black(CB)was added to increase the density of the graphite,and a fuel element(TRISO(tri-structural isotropic)fuel particles were randomly distributed in the modified graphite matrix)was prepared by cold isostatic pressing process.An out-of-pile performance study shows that the densification and pore structure of the modified graphite matrix were improved,as was the resistance to molten salt infiltration.The median pore size of the modified graphite was reduced from 673 to 433 nm and the threshold pressure for molten salt(FLiBe,66%(molar fraction)LiF and 34%BeF_(2))infiltration was increased from 0.88 to 1.37 MPa.The isotropic CB made the graphite matrix less anisotropic,while its thermal conductivity and compressive strength were reduced due to the difficult graphitization of CB.Fuel elements containing 20%(volume fraction)TRISO particles were prepared.Numerical simulations show that the power and temperature distribution of the fuel were in line with the design requirements.The modified graphite matrix had a higher density,smaller pores,a lower anisotropy and a greater resistance to FLiBe infiltration.
基金This work was supported by the National Key R&D Program of China(2022YFB4102000 and 2022YFA1505100)the NSFC(22472038)the Shanghai Science and Technology Innovation Action Plan(22dz1205500).
文摘Electrocatalytic carbon dioxide reduction is a promising technology for addressing global energy and environmental crises. However, its practical application faces two critical challenges: the complex and energy-intensive process of separat-ing mixed reduction products and the economic viability of the carbon sources (reactants) used. To tackle these challenges simultaneously, solid-state electrolyte (SSE) reactors are emerging as a promising solution. In this review, we focus on the feasibility of applying SSE for tandem electrochemical CO_(2) capture and conversion. The configurations and fundamental principles of SSE reactors are first discussed, followed by an introduction to its applications in these two specific areas, along with case studies on the implementation of tandem electrolysis. In comparison to conventional H-type cell, flow cell and membrane electrode assembly cell reactors, SSE reactors incorporate gas diffusion electrodes and utilize a solid electro-lyte layer positioned between an anion exchange membrane (AEM) and a cation exchange membrane (CEM). A key inno-vation of this design is the sandwiched SSE layer, which enhances efficient ion transport and facilitates continuous product extraction through a stream of deionized water or humidified nitrogen, effectively separating ion conduction from product collection. During electrolysis, driven by an electric field and concentration gradient, electrochemically generated ions (e.g., HCOO- and CH3COO-) migrate through the AEM into the SSE layer, while protons produced from water oxidation at the anode traverse the CEM into the central chamber to maintain charge balance. Targeted products like HCOOH can form in the middle layer through ionic recombination and are efficiently carried away by the flowing medium through the porous SSE layer, in the absence of electrolyte salt impurities. As CO_(2)RR can generate a series of liquid products, advancements in catalyst discovery over the past several years have facilitated the industrial application of SSE for more efficient chemicals production. Also noteworthy, the cathode reduction reaction can readily consume protons from water, creating a highly al-kaline local environment. SSE reactors are thereby employed to capture acidic CO_(2), forming CO_(3)^(2-) from various gas sources including flue gases. Driven by the electric field, the formed CO_(3)^(2-) can traverse through the AEM and react with protons originating from the anode, thereby regenerating CO_(2). This CO_(2) can then be collected and utilized as a low-cost feedstock for downstream CO_(2) electrolysis. Based on this principle, several cell configurations have been proposed to enhance CO_(2) capture from diverse gas sources. Through the collaboration of two SSE units, tandem electrochemical CO_(2) capture and con-version has been successfully implemented. Finally, we offer insights into the future development of SSE reactors for prac-tical applications aimed at achieving carbon neutrality. We recommend that greater attention be focused on specific aspects, including the fundamental physicochemical properties of the SSE layer, the electrochemical engineering perspective related to ion and species fluxes and selectivity, and the systematic pairing of consecutive CO_(2) capture and conversion units. These efforts aim to further enhance the practical application of SSE reactors within the broader electrochemistry community.
基金partly supported by the University of Shanghai for Science and Technology(No.10-24-301-101)。
文摘Liquid-fueled molten-salt reactors have dynamic features that distinguish them from solid-fueled reactors,such that conventional system-analysis codes are not directly applicable.In this study,a coupled dynamic model of the Molten-Salt Reactor Experiment(MSRE)is developed.The coupled model includes the neutronics and single-phase thermal-hydraulics modeling of the reactor and validated xenon-transport modeling from previous studies.The coupled dynamic model is validated against the frequency-response and transient-response data from the MSRE.The validated model is then applied to study the effects of xenon and void transport on the dynamic behaviors of the reactor.Plant responses during the unique initiating events such as off-gas system blockages and loss of circulating voids are investigated.
