Polystyrene nanoparticles pose significant toxicological risks to aquatic ecosystems,yet their impact on zebrafish(Danio rerio)embryonic development,particularly erythropoiesis,remains underexplored.This study used si...Polystyrene nanoparticles pose significant toxicological risks to aquatic ecosystems,yet their impact on zebrafish(Danio rerio)embryonic development,particularly erythropoiesis,remains underexplored.This study used single-cell RNA sequencing to comprehensively evaluate the effects of polystyrene nanoparticle exposure on erythropoiesis in zebrafish embryos.In vivo validation experiments corroborated the transcriptomic findings,revealing that polystyrene nanoparticle exposure disrupted erythrocyte differentiation,as evidenced by the decrease in mature erythrocytes and concomitant increase in immature erythrocytes.Additionally,impaired heme synthesis further contributed to the diminished erythrocyte population.These findings underscore the toxic effects of polystyrene nanoparticles on hematopoietic processes,highlighting their potential to compromise organismal health in aquatic environments.展开更多
Catalyst–support interaction plays a crucial role in improving the catalytic activity of oxygen evolution reaction(OER).Here we modulate the catalyst–support interaction in polyaniline-supported Ni_(3)Fe oxide(Ni_(3...Catalyst–support interaction plays a crucial role in improving the catalytic activity of oxygen evolution reaction(OER).Here we modulate the catalyst–support interaction in polyaniline-supported Ni_(3)Fe oxide(Ni_(3)Fe oxide/PANI)with a robust hetero-interface,which significantly improves oxygen evolution activities with an overpotential of 270 mV at 10 mA cm^(-2)and specific activity of 2.08 mA cm_(ECSA)^(-2)at overpotential of 300 mV,3.84-fold that of Ni_(3)Fe oxide.It is revealed that the catalyst–support interaction between Ni_(3)Fe oxide and PANI support enhances the Ni–O covalency via the interfacial Ni–N bond,thus promoting the charge and mass transfer on Ni_(3)Fe oxide.Considering the excellent activity and stability,rechargeable Zn-air batteries with optimum Ni_(3)Fe oxide/PANI are assembled,delivering a low charge voltage of 1.95 V to cycle for 400 h at 10 mA cm^(-2).The regulation of the effect of catalyst–support interaction on catalytic activity provides new possibilities for the future design of highly efficient OER catalysts.展开更多
The process of disposing of expanded polystyrene (EPS) is by burning it in municipal incinerators. This process gives off EPS microplastics, which can find their way into water, food, blood, and major organ systems. Z...The process of disposing of expanded polystyrene (EPS) is by burning it in municipal incinerators. This process gives off EPS microplastics, which can find their way into water, food, blood, and major organ systems. Zophobas morio larvae are capable of consuming and breaking down EPS within their digestive tracts by minimizing the spread of microplastics. Studies of the consumption of EPS by Z. morio larvae are typically conducted under white or no visible light treatments. This study tested whether the color of visible light influenced the consumption rate of EPS by Z. morio larvae. If Z. morio larvae consume EPS under visible light, then visible light will influence the amount of EPS consumed. If results suggest that the consumption rate is influenced by visible light colors, then Z. morio larvae could be a solution for recycling EPS. This study’s procedure placed Z. morio larvae into 25 jars under one of six visible light treatments of red, yellow, green, blue, white, and no visible light. Each jar contained a pre-weighed block of EPS and six Z. morio larvae. After two weeks, the Z. morio larvae were removed from the jars, and the difference between each pre-weighed EPS block and the weight of the same partially consumed block was recorded in three trials. The data indicates that green and blue visible light treatments resulted in the greatest amount of EPS consumed by Z. morio larvae while the red and yellow had the least amount of EPS consumed by the Z. morio larvae. In conclusion, results indicate that green and blue visible light, compared to the no visible light treatment, could be used to influence the Z. morio larvae to consume more EPS. Green and blue visible light and Z. morio larvae could make the recycling process of EPS more environmentally friendly when used in households or by local environmental organizations.展开更多
Polystyrene(PS)waste was depolymerized using a low-temperature pyrolysis treatment(LTPT)to increase its caking index.The mechanism of caking index modification was revealed by using Fourier transform infrared spectros...Polystyrene(PS)waste was depolymerized using a low-temperature pyrolysis treatment(LTPT)to increase its caking index.The mechanism of caking index modification was revealed by using Fourier transform infrared spectroscopy,thermogravimetric(TG)analysis,pyrolysis-gas chromatography with mass spectrometric detection,and solid-state^(13)C nuclear magnetic resonance spectroscopy.The crucible coal-blending coking tests were carried out using an industrial coal mixture and the treated-PS with the highest caking index(PS300)or raw PS.Some properties of the resultant cokes were also analyzed.It was demonstrated that the caking index of PS dramatically increased by LTPT;however,exceeding 300℃ did not yield any benefit.The caking index increased due to the formation of the caking components,whose molecules are medium in size,caused by LTPT.Additionally,the coke reactivity index of the coke obtained from the mixture containing PS300 decreased by 5.1%relative to that of the coke made from the mixture with PS and the coke strength after reaction index of the former increased by 7.3% compared with that of the latter,suggesting that the ratio of depolymerized PS used for coal-blending coking could increase relative to that of PS.展开更多
Mesoporous carbon supports mitigate platinum(Pt)sulfonic poisoning through nanopore-confined Pt deposition,yet their morphological impacts on oxygen transport remain unclear.This study integrates carbon support morpho...Mesoporous carbon supports mitigate platinum(Pt)sulfonic poisoning through nanopore-confined Pt deposition,yet their morphological impacts on oxygen transport remain unclear.This study integrates carbon support morphology simulation with an enhanced agglomerate model to establish a mathematical framework elucidating pore evolution,Pt utilization,and oxygen transport in catalyst layers.Results demonstrate dominant local mass transport resistance governed by three factors:(1)active site density dictating oxygen flux;(2)ionomer film thickness defining shortest transport path;(3)ionomer-to-Pt surface area ratio modulating practical pathway length.At low ionomer-to-carbon(I/C)ratios,limited active sites elevate resistance(Factor 1 dominant).Higher I/C ratios improve the ionomer coverage but eventually thicken ionomer films,degrading transport(Factors 2–3 dominant).The results indicate that larger carbon particles result in a net increase in local transport resistance by reducing external surface area and increasing ionomer thickness.As the proportion of Pt situated in nanopores or the Pt mass fraction increases,elevated Pt density inside the nanopores exacerbates pore blockage.This leads to the increased transport resistance by reducing active sites,and increasing ionomer thickness and surface area.Lower Pt loading linearly intensifies oxygen flux resistance.The model underscores the necessity to optimize support morphology,Pt distribution,and ionomer content to prevent pore blockage while balancing catalytic activity and transport efficiency.These insights provide a systematic approach for designing high-performance mesoporous carbon catalysts.展开更多
Polymethyl methacrylate(PMMA)is an optically transparent thermoplastic with favorable processing conditions.In this study,a series of plastic scintillators are prepared via thermal polymerization,and the impact of PMM...Polymethyl methacrylate(PMMA)is an optically transparent thermoplastic with favorable processing conditions.In this study,a series of plastic scintillators are prepared via thermal polymerization,and the impact of PMMA content on their transparency and pulse shape discrimination(PSD)ability is investigated.The fabricated samples,comprising a polystyrene(PS)-PMMA matrix,30.0 wt%2,5-diphenyloxazole(PPO),and 0.2 wt%9,10-diphenylanthracene(DPA),exhibit high transparency with transmissivity ranging from 70.0 to 90.0%(above 415.0 nm)and demonstrate excellent n/γdiscrimination capability.Transparency increased with increasing PMMA content across the entire visible light spectrum.However,the PSD performance gradually deteriorated when the aromatic matrix was replaced with PMMA.The scintillator containing 20.0 wt%PMMA demonstrated the best stability concerning PSD properties and relative light yields.展开更多
Nanoplastics exhibit greater environmental biotoxicity than microplastics and can be ingested by humans through major routes such as tap water,bottled water and other drinking water.Nanoplastics present a challenge fo...Nanoplastics exhibit greater environmental biotoxicity than microplastics and can be ingested by humans through major routes such as tap water,bottled water and other drinking water.Nanoplastics present a challenge for air flotation due to their minute particle size,negative surface potential,and similar density to water.This study employed dodecyltrimethylammonium chloride(DTAC)as a modifier to improve conventional air flotation,which significantly enhanced the removal of polystyrene nanoplastics(PSNPs).Conventional air flotation removed only 3.09%of PSNPs,while air flotation modified by dodecyltrimethylammonium chloride(DTAC-modified air flotation)increased the removal of PSNPs to 98.05%.The analysis of the DTAC-modified air flotation mechanism was conducted using a combination of instruments,including a zeta potential analyzer,contact angle meter,laser particle size meter,high definition camera,scanning electron microscope(SEM),energy dispersive spectrometer(EDS)and Fourier transform infrared spectrometer(FTIR).The results indicated that the incorporation of DTAC reversed the electrostatic repulsion between bubbles and PSNPs to electrostatic attraction,significantly enhancing the hydrophobic force in the system.This,in turn,improved the collision adhesion effect between bubbles and PSNPs.The experimental results indicated that even when the flotation time was reduced to 7min,the DTACmodified air flotation still achieved a high removal rate of 96.26%.Furthermore,changes in aeration,pH,and ionic strength did not significantly affect the performance of the modified air flotation for the removal of PSNPs.The removal rate of PSNPs in all three water bodies exceeded 95%.The DTAC-modified air flotation has excellent resistance to interference from complex conditions and shows great potential for practical application.展开更多
Compatibilization is crucial for the blending of immiscible polymers to develop high-performance composites;however,traditional compatibilization by copolymers(pre-made or in-situ generation)suffers from weak interfac...Compatibilization is crucial for the blending of immiscible polymers to develop high-performance composites;however,traditional compatibilization by copolymers(pre-made or in-situ generation)suffers from weak interface anchoring,and inorganic particles have gained extensive attention recently owing to their large interfacial desorption energy,while their low affinity to bulk components is a drawback.In this study,an interfacial atom transfer radical polymerization(ATRP)technique was employed to grow polystyrene(PS)and poly(2-hydroxyethyl methacrylate)(PHEMA)simultaneously on different hemispheres of Br-functionalized SiO_(2) nanoparticles to stabilize a Pickering emulsion,whereby a brush-type Janus nanoparticle(SiO_(2)@JNP)was developed.The polymer brushes were well-characterized,and the Janus feature was validated by transmission electron microscope(TEM)observation of the sole hemisphere grafting of SiO_(2)-PS as a control sample.SiO_(2)@JNP was demonstrated to be an efficient compatibilizer for a PS/poly(methyl methacrylate)(PMMA)immiscible blend,and the droplet-matrix morphology was significantly refined.The mechanical strength and toughness of the blend were synchronously enhanced at a low content SiO_(2)@JNP optimized~0.9 wt%,with the tensile strength,elongation at break and impact strength increased by 17.7%,26.6%and 19.6%,respectively.This enhancement may be attributed to the entanglements between the grafted polymer brushes and individual components that improve the particle-bulk phase affinity and enforce interfacial adhesion.展开更多
Microplastics(MPs)have garnered significant international scrutiny as an emerging environmental pollutant,constituting one of the four principal global environmental threats and posing potential health hazards to huma...Microplastics(MPs)have garnered significant international scrutiny as an emerging environmental pollutant,constituting one of the four principal global environmental threats and posing potential health hazards to humans.However,data on the impact of MPs on the early life of the commercially important fish remain limited.In this study,polystyrene microspheres(PS-MPs)(1 and 5μm)were used to investigate the effects of MPs on the growth,development,and metabolism in early life stages of large yellow croaker Pseudosciaena crocea.Results indicate that MPs were enriched in the gastrointestinal tract and gills of the fish.In addition,PS-MPs(1μm)exhibited no obvious effects on embryo hatching and heart rates,while increased the mortality rate(23.00%vs.control 14.99%)and decreased the body length(4098.61±447.03μm vs.control with 2827.04±254.75μm)of the larvae at the highest exposure concentration(5×10^(4)items/L).Metabolomics analysis revealed that PS-MPs(5μm)induced mild perturbations in phospholipid metabolism,specifically alterations in phosphatidylethanolamine(PE)levels.These changes influenced the cell membranes of juvenile fish,and consequently elicited inflammatory responses,disrupted lipid homeostasis,and affected other critical physiological processes.Ultimately,these effects may avoid the growth retardation and potential mortality.Therefore,PS-MPs could affect negatively the fish health in the early life stage,which has implications for aquatic ecosystems.展开更多
The adsorption kinetics of polystyrene[1-butyl-3-methylimidazolium][bis(2,4,4-trimethylpentyl)phosphinate](PS[C_(4)mim][C272])towards V(V)in acidic leachate was explored under ultrasound.The effects of ultrasonic powe...The adsorption kinetics of polystyrene[1-butyl-3-methylimidazolium][bis(2,4,4-trimethylpentyl)phosphinate](PS[C_(4)mim][C272])towards V(V)in acidic leachate was explored under ultrasound.The effects of ultrasonic power and V(V)concentration on the adsorption performance of PS[C_(4)mim][C272]were investigated.The results showed that ultrasonic radiation significantly shortened the adsorption equilibrium time and improved the adsorption performance of PS[C_(4)mim][C272]compared with the conventional oscillation.At an ultrasonic power of 200 W,the equilibrium adsorption capacity of PS[C_(4)mim][C272]reached its maximum of 311.58 mg/g.The kinetic model fitting results showed that the adsorption process of PS[C_(4)mim][C272]strictly followed the pseudo-second-order kinetic model under ultrasound.Analysis using the shrinking core model and the Weber−Morris model showed that the adsorption process of PS[C_(4)mim][C272]was primarily controlled by intra-particle diffusion mechanism.The adsorption isotherm model study showed that the Langmuir isotherm model could effectively fit the adsorption process of PS[C_(4)mim][C272]under ultrasound.展开更多
Carbon-supported mercury catalysts are extensivelyemployed in calcium carbide-based polyvinyl chloride(PVC)industries,but the usage of mercury-based catalysts can pose an environmental threat due to the release of mer...Carbon-supported mercury catalysts are extensivelyemployed in calcium carbide-based polyvinyl chloride(PVC)industries,but the usage of mercury-based catalysts can pose an environmental threat due to the release of mercury into the surrounding area during the operation period.In this study,a highly active and stable mercury-based catalyst was developed,utilizing the nitrogen atom of the support as the anchor site to enhance the interaction between active sites(HgCl_(2))and the carbon support(N-AC).Thermal loss rate testing and thermogravimetric analysis results demonstrate that,compared to commercial activated carbon,N-doped carbon can effectively increase the heat stability of HgCl_(2).The obtained mercury-based catalysts(HgCl_(2)/N-AC)exhibit significant catalytic performance,achieving 2.5 times the C2H2 conversion of conventional HgCl_(2)/AC catalysts.Experimental analysis combined with theoretical calculations reveals that,contrary to the Eley-Rideal(ER)mechanism of HgCl_(2)/AC,the HgCl_(2)/N-AC catalyst follows the Langmuir-Hinshelwood(LH)adsorption mechanism.The nitrogen sites and HgCl_(2) on the catalyst enhance the adsorption capabilities of the HCl and C2H2,thereby improving the catalytic performance.Based on the modification of the active center by these solid ligands,the loading amount of HgCl_(2) on the catalyst can be further reduced from the current 6.5%to 3%.Considering the absence of successful industrial applications for mercury-free catalysts,and based on the current annual consumption of commercial mercury chloride catalysts in the PVC industry,the widespread adoption of this technology could annually reduce the usage of chlorine mercury by 500 tons,making a notable contribution to mercury compliance,reduction,and emissions control in China.It also serves as a bridge between mercury-free and low-mercury catalysts.Moreover,this solid ligand technology can assist in the application research of mercury-free catalysts.展开更多
Herein,three supported catalysts,CuO/Al_(2)O_(3),CeO_(2)/Al_(2)O_(3),and CuO-CeO_(2)/Al_(2)O_(3),were synthesized by the convenient impregnation method to reveal the effect of CeO_(2)addition on catalytic performance ...Herein,three supported catalysts,CuO/Al_(2)O_(3),CeO_(2)/Al_(2)O_(3),and CuO-CeO_(2)/Al_(2)O_(3),were synthesized by the convenient impregnation method to reveal the effect of CeO_(2)addition on catalytic performance and reaction mechanism for toluene oxidation.Compared with CuO/Al_(2)O_(3),the T_(50)and T_(90)(the temperatures at 50%and 90%toluene conversion,respectively)of CuO-CeO_(2)/Al_(2)O_(3)were reduced by 33 and 39°C,respectively.N_(2)adsorptiondesorption experiment,XRD,SEM,EDS mapping,Raman,EPR,H_(2)-TPR,O_(2)-TPD,XPS,NH_(3)-TPD,Toluene-TPD,and in-situ DRIFTS were conducted to characterize these catalysts.The excellent catalytic performance of CuO-CeO_(2)/Al_(2)O_(3)could be attributed to its strong coppercerium interaction and high oxygen vacancies concentration.Moreover,in-situ DRIFTS proved that CuO-CeO_(2)/Al_(2)O_(3)promoted the conversion of toluene to benzoate and accelerated the deep degradation path of toluene.This work provided valuable insights into the development of efficient and economical catalysts for volatile organic compounds.展开更多
This article analyzes the design of a variable-height simply supported steel truss bridge based on an actual project.It includes its basic situation,introduction to variable-height simply supported steel truss bridges...This article analyzes the design of a variable-height simply supported steel truss bridge based on an actual project.It includes its basic situation,introduction to variable-height simply supported steel truss bridges,key design points of such bridges,and finite element analysis of the design effect.The analysis shows that for such bridges,reasonable main structure design and node design are the keys to determining the overall design idea,and through the reasonable application of the finite element analysis method,the design effect can be scientifically determined,providing a reference for the subsequent structural design of such projects.展开更多
Single-walled carbon nanotubes(SWNTs)with enriched(n,m)species are in high demand for various advanced applications.Since the SWNT structure is largely influenced by the chemistry of the active catalyst during growth ...Single-walled carbon nanotubes(SWNTs)with enriched(n,m)species are in high demand for various advanced applications.Since the SWNT structure is largely influenced by the chemistry of the active catalyst during growth process,exploiting novel catalyst with bias towards specific SWNT chiralities has been challenging.In this work,we introduce a vanadium catalyst supported by mesoporous magnesia(V-MgO)for the selective growth of SWNTs using CO chemical vapor deposition(CVD).At a reaction temperature of 650℃,the(6,5)SWNT content reaches an impressive 67.9%among all semiconducting species,exceeding the selectivity of many commercial SWNT products.Post-CVD analysis reveals that the catalyst transforms into vanadium carbide(VC),which acts as a nucleation site for SWNT growth.Molecular dynamics simulations indicate that the energy at the SWNT-VC interface and the growth kinetics of SWNTs contribute to the chirality selectivity.This research opens up possibilities for the selective synthesis of SWNTs using cost-effective early transition metals,illuminating their future applications in fields such as bioimaging.展开更多
This paper investigates the active traveling wave vibration control of an elastic supported rotating porous aluminium conical shell(CS)under impact loading.Piezoelectric smart materials in the form of micro fiber comp...This paper investigates the active traveling wave vibration control of an elastic supported rotating porous aluminium conical shell(CS)under impact loading.Piezoelectric smart materials in the form of micro fiber composites(MFCs)are used as actuators and sensors.To this end,a metal pore truncated CS with MFCs attached to its surface is considered.Adding artificial virtual springs at two edges of the truncated CS achieves various elastic supported boundaries by changing the spring stiffness.Based on the first-order shear deformation theory(FSDT),minimum energy principle,and artificial virtual spring technology,the theoretical formulations considering the electromechanical coupling are derived.The comparison of the natural frequency of the present results with the natural frequencies reported in previous literature evaluates the accuracy of the present approach.To study the vibration control,the integral quadrature method in conjunction with the differential quadrature approximation in the length direction is used to discretize the partial differential dynamical system to form a set of ordinary differential equations.With the aid of the velocity negative feedback method,both the time history and the input control voltage on the actuator are demonstrated to present the effects of velocity feedback gain,pore distribution type,semi-vertex angle,impact loading,and rotational angular velocity on the traveling wave vibration control.展开更多
Selective hydrogenation of furfural to furfuryl alcohol is a great challenge in the hydrogenation field due to thermodynamic preference for hydrogenation of C=C over C=O.Herein,a novel Al_(2)O_(3)/C-u hybrid catalyst,...Selective hydrogenation of furfural to furfuryl alcohol is a great challenge in the hydrogenation field due to thermodynamic preference for hydrogenation of C=C over C=O.Herein,a novel Al_(2)O_(3)/C-u hybrid catalyst,composed of N-modified dendritic carbon networks supporting Al_(2)O_(3)nanoparticles,was successfully prepared via carbonizing the freeze-dried gel from spontaneous cross-linking of alginate,Al3+and urea.The obtained carbon-supported Al_(2)O_(3)hybrid catalyst has a high ratio (31%) of Al species in pentahedral-coordinated state.The introduction of urea enhances the surface N content,the ratio of pyrrolic N,and specific surface area of catalyst,leading to improved adsorption capacity of C=O and the accessibility of active sites.In the furfural hydrogenation reaction with isopropyl alcohol as hydrogen donor,Al_(2)O_(3)/C-u catalyst achieved a 90%conversion of furfural with 98.0% selectivity to furfuryl alcohol,outperforming that of commercial γ-Al_(2)O_(3).Moreover,Al_(2)O_(3)/C-u demonstrates excellent catalytic stability in the recycling tests attributed to the synergistic effect of abundant weak Lewis acid sites and the anchoring effect of the carbon network on Al_(2)O_(3)nanoparticles.This work provides an innovative and facile strategy for fabrication of carbon-supported Al_(2)O_(3)hybrid catalysts with rich AlVspecies,serving as a high selective hydrogenation catalyst through MPV reaction route.展开更多
The imperative demand for energy paradigm shift toward renewable and sustainable energy sources has intensified interest in proton exchange membrane water electrolysis(PEMWE)as a clean and efficient hydrogen productio...The imperative demand for energy paradigm shift toward renewable and sustainable energy sources has intensified interest in proton exchange membrane water electrolysis(PEMWE)as a clean and efficient hydrogen production technology.However,the practical application of PEMWE is hindered by the scarcity and high cost of iridium(Ir),the state-of-the-art electrocatalyst for the oxygen evolution reaction(OER).To reduce Ir loading without compromising performance,we report a novel hollow Bi_(2)Te_(3)(h-Bi_(2)Te_(3))nanowire as a conductive and acid-tolerant support for Ir-based OER electrocatalysts.The h-Bi_(2)Te_(3) nanowires were synthesized via a two-step wet chemical synthesis involving Te nanowire growth and subsequent Bi incorporation,with controlled hollowness induced by modulating the reducing agent concentration.Ir nanoparticles were uniformly deposited onto h-Bi_(2)Te_(3) via polyol method,forming amorphous and well-dispersed Ir catalytic layers.Ir/h-Bi_(2)Te_(3) catalyst achieved an outstanding OER overpotential of 268 mV at 10 mA/cm^(2),a mass activity of 460 mA/mgIr at 1.55 V(vs.reversible hydrogen electrode(RHE)),and superior stability over 5 h,surpassing commercial IrO_(x)/TiO_(2),commercial Ir black,and Ir/Te benchmarks.The enhanced performance was attributed to the strong metal-support interaction,improved charge transfer,and enlarged electrochemically active surface area.Moreover,Ir/h-Bi_(2)Te_(3) catalyst demonstrated outstanding single-cell performance of 1.811 V at 2.0 A/cm^(2) with extremely low Ir loading(0.1 mgIr/cm^(2))and long-term durability(a cell voltage increase of 36.6 mV during 100 h at 1.0 A/cm^(2)),confirming its strong potential as a practical anode electrocatalyst for PEMWE.This study highlights the promise of morphology-engineered h-Bi_(2)Te_(3) supports for advancing cost-effective and durable PEMWE systems.展开更多
The expandable graphite(EG)modified TiO_(2) nanocomposites were prepared by the high shearmethod using the TiO_(2) nanoparticles(NPs)and EG as precursors,in which the amount of EG doped in TiO_(2) was 10 wt.%.Followed...The expandable graphite(EG)modified TiO_(2) nanocomposites were prepared by the high shearmethod using the TiO_(2) nanoparticles(NPs)and EG as precursors,in which the amount of EG doped in TiO_(2) was 10 wt.%.Followed by the impregnation method,adjusting the pH of the solution to 10,and using the electrostatic adsorption to achieve spatial confinement,the Pt elementswere mainly distributed on the exposed TiO_(2),thus generating the Pt/10EG-TiO_(2)-10 catalyst.The best CO oxidation activity with the excellent resistance to H_(2)O and SO_(2) was obtained over the Pt/10EG-TiO_(2)-10 catalyst:CO conversion after 36 hr of the reaction was ca.85%under the harsh condition of 10 vol.%H_(2)O and 100 ppm SO_(2) at a high gaseous hourly space velocity(GHSV)of 400,000 hr−1.Physicochemical properties of the catalystswere characterized by various techniques.The results showed that the electrostatic adsorption,which riveted the Pt elements mainly on the exposed TiO_(2) of the support surface,reduced the dispersion of Pt NPs on EG and achieved the effective dispersion of Pt NPs,hence significantly improving CO oxidation activity over the Pt/10EG-TiO_(2)-10 catalyst.The 10 wt.%EG doped in TiO_(2) caused the TiO_(2) support to form a more hydrophobic surface,which reduced the adsorption of H_(2)O and SO_(2) on the catalyst,greatly inhibited deposition of the TiOSO_(4) and formation of the PtSO4 species as well as suppressed the oxidation of SO_(2),thus resulting in an improvement in the resistance to H_(2)O and SO_(2) of the Pt/10EG-TiO_(2)-10 catalyst.展开更多
Volatile organic compounds(VOCs)exhausted from industrial processes are the major atmospheric pollutants,which could destroy the ecological environment and make hazards to human health seriously.Catalytic oxidation is...Volatile organic compounds(VOCs)exhausted from industrial processes are the major atmospheric pollutants,which could destroy the ecological environment and make hazards to human health seriously.Catalytic oxidation is regarded as the most competitive strategy for the efficient elimination of low-concentration VOCs.Supported noble metal catalysts are preferred catalysts due to their excellent low-temperature catalytic activity.To further lower the cost of catalysts,single atom catalysts(SAC)have been fabricated and extensively studied for application in VOCs oxidation due to their 100%atom-utilization efficiency and unique catalytic performance.In this review,we comprehensively summarize the recent advances in supported noble metal(e.g.,Pt,Pd,Au,and Ag)catalysts and SAC for VOCs oxidation since 2015.Firstly,this paper focuses on some important influencing factors that affect the activity of supported noble metal catalysts,including particle size,valence state and dispersion of noble metals,properties of the support,metal oxide/ion modification,preparation method,and pretreatment conditions of catalysts.Secondly,we briefly summarize the catalytic performance of SAC for typical VOCs.Finally,we conclude the key influencing factors and provide the prospects and challenges of VOCs oxidation.展开更多
Molybdenum (VI) complex, namely molybdenum dioxobis(2,4-pentanedione) [MoO2(acac)2] used as epoxidation catalyst species, was synthesized and characterized by elemental analysis and infrared spectrum. Polystyrene-supp...Molybdenum (VI) complex, namely molybdenum dioxobis(2,4-pentanedione) [MoO2(acac)2] used as epoxidation catalyst species, was synthesized and characterized by elemental analysis and infrared spectrum. Polystyrene-supported molybdenum dioxobis(2,4-pentanedione) [MoO2(acac)2] for synthesis of epoxycyclohexane was prepared by phase transfer catalysis method. Effects of various factors in synthesis of epoxycyclohexane by reaction of cyclohexene and t-BuOOH in the atmosphere of nitrogen catalyzed by polystyrene-supported MoO2(acac)2 were also investigated. Under the following conditions, n(cyclohexene):n(t-BuOOH)=3.5:l (based on 0.1 mol of t-BuOOH), volume of solvent -10ml, reaction temperature -80℃, reaction time -60min, and mass of molybdenum in the catalyst -2.30×0^(-3)g, the yield of epoxycyclohexane on the basis of t-BuOOH is over 99.5%, and the purity of epoxycyclohexane is about 99.9% by gas chromatogram(GC) analysis.展开更多
基金supported by the Institute for Basic Science (IBS-R022-D1)Global Learning&Academic Research Institution for Master’s/Ph D students and Post-Doc Program of the National Research Foundation of Korea Grant funded by the Ministry of Education (RS-2023-00301938)+1 种基金National Research Foundation of Korea Grant funded by the Korean government (RS-2024-00406152,MSIT)Additional financial support was provided by the 2024 Post-Doc Development Program of Pusan National University,Korea Medical Institute,and KREONET。
文摘Polystyrene nanoparticles pose significant toxicological risks to aquatic ecosystems,yet their impact on zebrafish(Danio rerio)embryonic development,particularly erythropoiesis,remains underexplored.This study used single-cell RNA sequencing to comprehensively evaluate the effects of polystyrene nanoparticle exposure on erythropoiesis in zebrafish embryos.In vivo validation experiments corroborated the transcriptomic findings,revealing that polystyrene nanoparticle exposure disrupted erythrocyte differentiation,as evidenced by the decrease in mature erythrocytes and concomitant increase in immature erythrocytes.Additionally,impaired heme synthesis further contributed to the diminished erythrocyte population.These findings underscore the toxic effects of polystyrene nanoparticles on hematopoietic processes,highlighting their potential to compromise organismal health in aquatic environments.
基金Research Institute for Smart Energy(CDB2)the grant from the Research Institute for Advanced Manufacturing(CD8Z)+4 种基金the grant from the Carbon Neutrality Funding Scheme(WZ2R)at The Hong Kong Polytechnic Universitysupport from the Hong Kong Polytechnic University(CD9B,CDBZ and WZ4Q)the National Natural Science Foundation of China(22205187)Shenzhen Municipal Science and Technology Innovation Commission(JCYJ20230807140402006)Start-up Foundation for Introducing Talent of NUIST and Natural Science Foundation of Jiangsu Province of China(BK20230426).
文摘Catalyst–support interaction plays a crucial role in improving the catalytic activity of oxygen evolution reaction(OER).Here we modulate the catalyst–support interaction in polyaniline-supported Ni_(3)Fe oxide(Ni_(3)Fe oxide/PANI)with a robust hetero-interface,which significantly improves oxygen evolution activities with an overpotential of 270 mV at 10 mA cm^(-2)and specific activity of 2.08 mA cm_(ECSA)^(-2)at overpotential of 300 mV,3.84-fold that of Ni_(3)Fe oxide.It is revealed that the catalyst–support interaction between Ni_(3)Fe oxide and PANI support enhances the Ni–O covalency via the interfacial Ni–N bond,thus promoting the charge and mass transfer on Ni_(3)Fe oxide.Considering the excellent activity and stability,rechargeable Zn-air batteries with optimum Ni_(3)Fe oxide/PANI are assembled,delivering a low charge voltage of 1.95 V to cycle for 400 h at 10 mA cm^(-2).The regulation of the effect of catalyst–support interaction on catalytic activity provides new possibilities for the future design of highly efficient OER catalysts.
文摘The process of disposing of expanded polystyrene (EPS) is by burning it in municipal incinerators. This process gives off EPS microplastics, which can find their way into water, food, blood, and major organ systems. Zophobas morio larvae are capable of consuming and breaking down EPS within their digestive tracts by minimizing the spread of microplastics. Studies of the consumption of EPS by Z. morio larvae are typically conducted under white or no visible light treatments. This study tested whether the color of visible light influenced the consumption rate of EPS by Z. morio larvae. If Z. morio larvae consume EPS under visible light, then visible light will influence the amount of EPS consumed. If results suggest that the consumption rate is influenced by visible light colors, then Z. morio larvae could be a solution for recycling EPS. This study’s procedure placed Z. morio larvae into 25 jars under one of six visible light treatments of red, yellow, green, blue, white, and no visible light. Each jar contained a pre-weighed block of EPS and six Z. morio larvae. After two weeks, the Z. morio larvae were removed from the jars, and the difference between each pre-weighed EPS block and the weight of the same partially consumed block was recorded in three trials. The data indicates that green and blue visible light treatments resulted in the greatest amount of EPS consumed by Z. morio larvae while the red and yellow had the least amount of EPS consumed by the Z. morio larvae. In conclusion, results indicate that green and blue visible light, compared to the no visible light treatment, could be used to influence the Z. morio larvae to consume more EPS. Green and blue visible light and Z. morio larvae could make the recycling process of EPS more environmentally friendly when used in households or by local environmental organizations.
基金supported by the National Natural Science Foundation of China(22308006 and 22278001)the Natural Science Foundation of Anhui Provincial Education Department(KJ2021A0407).
文摘Polystyrene(PS)waste was depolymerized using a low-temperature pyrolysis treatment(LTPT)to increase its caking index.The mechanism of caking index modification was revealed by using Fourier transform infrared spectroscopy,thermogravimetric(TG)analysis,pyrolysis-gas chromatography with mass spectrometric detection,and solid-state^(13)C nuclear magnetic resonance spectroscopy.The crucible coal-blending coking tests were carried out using an industrial coal mixture and the treated-PS with the highest caking index(PS300)or raw PS.Some properties of the resultant cokes were also analyzed.It was demonstrated that the caking index of PS dramatically increased by LTPT;however,exceeding 300℃ did not yield any benefit.The caking index increased due to the formation of the caking components,whose molecules are medium in size,caused by LTPT.Additionally,the coke reactivity index of the coke obtained from the mixture containing PS300 decreased by 5.1%relative to that of the coke made from the mixture with PS and the coke strength after reaction index of the former increased by 7.3% compared with that of the latter,suggesting that the ratio of depolymerized PS used for coal-blending coking could increase relative to that of PS.
基金supported by the Program of Ministry of Science and Technology of China(No.2023YFB2504200)support of Shanghai Rising-Star Program(Grant No.24QB2703200)the Major Science and Technology Projects of Yunnan Province(No.202302AH360001).
文摘Mesoporous carbon supports mitigate platinum(Pt)sulfonic poisoning through nanopore-confined Pt deposition,yet their morphological impacts on oxygen transport remain unclear.This study integrates carbon support morphology simulation with an enhanced agglomerate model to establish a mathematical framework elucidating pore evolution,Pt utilization,and oxygen transport in catalyst layers.Results demonstrate dominant local mass transport resistance governed by three factors:(1)active site density dictating oxygen flux;(2)ionomer film thickness defining shortest transport path;(3)ionomer-to-Pt surface area ratio modulating practical pathway length.At low ionomer-to-carbon(I/C)ratios,limited active sites elevate resistance(Factor 1 dominant).Higher I/C ratios improve the ionomer coverage but eventually thicken ionomer films,degrading transport(Factors 2–3 dominant).The results indicate that larger carbon particles result in a net increase in local transport resistance by reducing external surface area and increasing ionomer thickness.As the proportion of Pt situated in nanopores or the Pt mass fraction increases,elevated Pt density inside the nanopores exacerbates pore blockage.This leads to the increased transport resistance by reducing active sites,and increasing ionomer thickness and surface area.Lower Pt loading linearly intensifies oxygen flux resistance.The model underscores the necessity to optimize support morphology,Pt distribution,and ionomer content to prevent pore blockage while balancing catalytic activity and transport efficiency.These insights provide a systematic approach for designing high-performance mesoporous carbon catalysts.
基金supported by the National Natural Science Foundation of China(No.12027813)the fund of National Innovation Center of Radiation Application of China(Nos.KFZC2020020501,KFZC2021010101).
文摘Polymethyl methacrylate(PMMA)is an optically transparent thermoplastic with favorable processing conditions.In this study,a series of plastic scintillators are prepared via thermal polymerization,and the impact of PMMA content on their transparency and pulse shape discrimination(PSD)ability is investigated.The fabricated samples,comprising a polystyrene(PS)-PMMA matrix,30.0 wt%2,5-diphenyloxazole(PPO),and 0.2 wt%9,10-diphenylanthracene(DPA),exhibit high transparency with transmissivity ranging from 70.0 to 90.0%(above 415.0 nm)and demonstrate excellent n/γdiscrimination capability.Transparency increased with increasing PMMA content across the entire visible light spectrum.However,the PSD performance gradually deteriorated when the aromatic matrix was replaced with PMMA.The scintillator containing 20.0 wt%PMMA demonstrated the best stability concerning PSD properties and relative light yields.
基金supported by Science&Technology Department of Sichuan Province(No.2023YFS0389)Chengdu Technology Innovation Research and Development Project of Chengdu Science and Technology Bureau(No.2022-YF05-00307-SN).
文摘Nanoplastics exhibit greater environmental biotoxicity than microplastics and can be ingested by humans through major routes such as tap water,bottled water and other drinking water.Nanoplastics present a challenge for air flotation due to their minute particle size,negative surface potential,and similar density to water.This study employed dodecyltrimethylammonium chloride(DTAC)as a modifier to improve conventional air flotation,which significantly enhanced the removal of polystyrene nanoplastics(PSNPs).Conventional air flotation removed only 3.09%of PSNPs,while air flotation modified by dodecyltrimethylammonium chloride(DTAC-modified air flotation)increased the removal of PSNPs to 98.05%.The analysis of the DTAC-modified air flotation mechanism was conducted using a combination of instruments,including a zeta potential analyzer,contact angle meter,laser particle size meter,high definition camera,scanning electron microscope(SEM),energy dispersive spectrometer(EDS)and Fourier transform infrared spectrometer(FTIR).The results indicated that the incorporation of DTAC reversed the electrostatic repulsion between bubbles and PSNPs to electrostatic attraction,significantly enhancing the hydrophobic force in the system.This,in turn,improved the collision adhesion effect between bubbles and PSNPs.The experimental results indicated that even when the flotation time was reduced to 7min,the DTACmodified air flotation still achieved a high removal rate of 96.26%.Furthermore,changes in aeration,pH,and ionic strength did not significantly affect the performance of the modified air flotation for the removal of PSNPs.The removal rate of PSNPs in all three water bodies exceeded 95%.The DTAC-modified air flotation has excellent resistance to interference from complex conditions and shows great potential for practical application.
基金financially supported by the National Natural Science Foundation of China(Nos.22172028,21903015,and 22403017)Natural Science Foundation of Fujian Province of China(No.2022J05041)。
文摘Compatibilization is crucial for the blending of immiscible polymers to develop high-performance composites;however,traditional compatibilization by copolymers(pre-made or in-situ generation)suffers from weak interface anchoring,and inorganic particles have gained extensive attention recently owing to their large interfacial desorption energy,while their low affinity to bulk components is a drawback.In this study,an interfacial atom transfer radical polymerization(ATRP)technique was employed to grow polystyrene(PS)and poly(2-hydroxyethyl methacrylate)(PHEMA)simultaneously on different hemispheres of Br-functionalized SiO_(2) nanoparticles to stabilize a Pickering emulsion,whereby a brush-type Janus nanoparticle(SiO_(2)@JNP)was developed.The polymer brushes were well-characterized,and the Janus feature was validated by transmission electron microscope(TEM)observation of the sole hemisphere grafting of SiO_(2)-PS as a control sample.SiO_(2)@JNP was demonstrated to be an efficient compatibilizer for a PS/poly(methyl methacrylate)(PMMA)immiscible blend,and the droplet-matrix morphology was significantly refined.The mechanical strength and toughness of the blend were synchronously enhanced at a low content SiO_(2)@JNP optimized~0.9 wt%,with the tensile strength,elongation at break and impact strength increased by 17.7%,26.6%and 19.6%,respectively.This enhancement may be attributed to the entanglements between the grafted polymer brushes and individual components that improve the particle-bulk phase affinity and enforce interfacial adhesion.
基金Supported by the Pioneer and Leading Goose R&D Program of Zhejiang(No.2023C03130)the National Key R&D Program of China(No.2019YFD0901101)+4 种基金the National Natural Science Foundation of China(No.42076169)the Oceanic Interdisciplinary Program of Shanghai Jiao Tong University(Nos.SL2022ZD203,SL2022MS012)the Zhejiang Provincial Natural Science Founds for Distinguished Young Scientists(No.LR21D060001)the State Key Laboratory of Satellite Ocean Environment Dynamics(No.SOEDZZ1902)the ChinaAPEC Cooperation Fund(No.2029901)。
文摘Microplastics(MPs)have garnered significant international scrutiny as an emerging environmental pollutant,constituting one of the four principal global environmental threats and posing potential health hazards to humans.However,data on the impact of MPs on the early life of the commercially important fish remain limited.In this study,polystyrene microspheres(PS-MPs)(1 and 5μm)were used to investigate the effects of MPs on the growth,development,and metabolism in early life stages of large yellow croaker Pseudosciaena crocea.Results indicate that MPs were enriched in the gastrointestinal tract and gills of the fish.In addition,PS-MPs(1μm)exhibited no obvious effects on embryo hatching and heart rates,while increased the mortality rate(23.00%vs.control 14.99%)and decreased the body length(4098.61±447.03μm vs.control with 2827.04±254.75μm)of the larvae at the highest exposure concentration(5×10^(4)items/L).Metabolomics analysis revealed that PS-MPs(5μm)induced mild perturbations in phospholipid metabolism,specifically alterations in phosphatidylethanolamine(PE)levels.These changes influenced the cell membranes of juvenile fish,and consequently elicited inflammatory responses,disrupted lipid homeostasis,and affected other critical physiological processes.Ultimately,these effects may avoid the growth retardation and potential mortality.Therefore,PS-MPs could affect negatively the fish health in the early life stage,which has implications for aquatic ecosystems.
基金financially supported by the National Natural Science Foundation of China(No.52074204)Key R&D Program of Zhejiang Province,China(No.2022C03061)。
文摘The adsorption kinetics of polystyrene[1-butyl-3-methylimidazolium][bis(2,4,4-trimethylpentyl)phosphinate](PS[C_(4)mim][C272])towards V(V)in acidic leachate was explored under ultrasound.The effects of ultrasonic power and V(V)concentration on the adsorption performance of PS[C_(4)mim][C272]were investigated.The results showed that ultrasonic radiation significantly shortened the adsorption equilibrium time and improved the adsorption performance of PS[C_(4)mim][C272]compared with the conventional oscillation.At an ultrasonic power of 200 W,the equilibrium adsorption capacity of PS[C_(4)mim][C272]reached its maximum of 311.58 mg/g.The kinetic model fitting results showed that the adsorption process of PS[C_(4)mim][C272]strictly followed the pseudo-second-order kinetic model under ultrasound.Analysis using the shrinking core model and the Weber−Morris model showed that the adsorption process of PS[C_(4)mim][C272]was primarily controlled by intra-particle diffusion mechanism.The adsorption isotherm model study showed that the Langmuir isotherm model could effectively fit the adsorption process of PS[C_(4)mim][C272]under ultrasound.
基金supported by the National Key Research and Development Program of China(2024YFC3907904).
文摘Carbon-supported mercury catalysts are extensivelyemployed in calcium carbide-based polyvinyl chloride(PVC)industries,but the usage of mercury-based catalysts can pose an environmental threat due to the release of mercury into the surrounding area during the operation period.In this study,a highly active and stable mercury-based catalyst was developed,utilizing the nitrogen atom of the support as the anchor site to enhance the interaction between active sites(HgCl_(2))and the carbon support(N-AC).Thermal loss rate testing and thermogravimetric analysis results demonstrate that,compared to commercial activated carbon,N-doped carbon can effectively increase the heat stability of HgCl_(2).The obtained mercury-based catalysts(HgCl_(2)/N-AC)exhibit significant catalytic performance,achieving 2.5 times the C2H2 conversion of conventional HgCl_(2)/AC catalysts.Experimental analysis combined with theoretical calculations reveals that,contrary to the Eley-Rideal(ER)mechanism of HgCl_(2)/AC,the HgCl_(2)/N-AC catalyst follows the Langmuir-Hinshelwood(LH)adsorption mechanism.The nitrogen sites and HgCl_(2) on the catalyst enhance the adsorption capabilities of the HCl and C2H2,thereby improving the catalytic performance.Based on the modification of the active center by these solid ligands,the loading amount of HgCl_(2) on the catalyst can be further reduced from the current 6.5%to 3%.Considering the absence of successful industrial applications for mercury-free catalysts,and based on the current annual consumption of commercial mercury chloride catalysts in the PVC industry,the widespread adoption of this technology could annually reduce the usage of chlorine mercury by 500 tons,making a notable contribution to mercury compliance,reduction,and emissions control in China.It also serves as a bridge between mercury-free and low-mercury catalysts.Moreover,this solid ligand technology can assist in the application research of mercury-free catalysts.
基金supported by the Science and Technology Program of Guangzhou,China(No.202002020020)the National Natural Science Foundation of China(Nos.51878292 and 42002035).
文摘Herein,three supported catalysts,CuO/Al_(2)O_(3),CeO_(2)/Al_(2)O_(3),and CuO-CeO_(2)/Al_(2)O_(3),were synthesized by the convenient impregnation method to reveal the effect of CeO_(2)addition on catalytic performance and reaction mechanism for toluene oxidation.Compared with CuO/Al_(2)O_(3),the T_(50)and T_(90)(the temperatures at 50%and 90%toluene conversion,respectively)of CuO-CeO_(2)/Al_(2)O_(3)were reduced by 33 and 39°C,respectively.N_(2)adsorptiondesorption experiment,XRD,SEM,EDS mapping,Raman,EPR,H_(2)-TPR,O_(2)-TPD,XPS,NH_(3)-TPD,Toluene-TPD,and in-situ DRIFTS were conducted to characterize these catalysts.The excellent catalytic performance of CuO-CeO_(2)/Al_(2)O_(3)could be attributed to its strong coppercerium interaction and high oxygen vacancies concentration.Moreover,in-situ DRIFTS proved that CuO-CeO_(2)/Al_(2)O_(3)promoted the conversion of toluene to benzoate and accelerated the deep degradation path of toluene.This work provided valuable insights into the development of efficient and economical catalysts for volatile organic compounds.
文摘This article analyzes the design of a variable-height simply supported steel truss bridge based on an actual project.It includes its basic situation,introduction to variable-height simply supported steel truss bridges,key design points of such bridges,and finite element analysis of the design effect.The analysis shows that for such bridges,reasonable main structure design and node design are the keys to determining the overall design idea,and through the reasonable application of the finite element analysis method,the design effect can be scientifically determined,providing a reference for the subsequent structural design of such projects.
基金financially supported by the Key Basic Research Project of Shandong Province(No.ZR2019ZD49)Taishan Scholar Foundation of Shandong Province(No.tstp20230627)Open Research Fund of State Key Laboratory of Polymer Physics and Chemistry,Changchun Institute of Applied Chemistry,Chinese Academy of Sciences。
文摘Single-walled carbon nanotubes(SWNTs)with enriched(n,m)species are in high demand for various advanced applications.Since the SWNT structure is largely influenced by the chemistry of the active catalyst during growth process,exploiting novel catalyst with bias towards specific SWNT chiralities has been challenging.In this work,we introduce a vanadium catalyst supported by mesoporous magnesia(V-MgO)for the selective growth of SWNTs using CO chemical vapor deposition(CVD).At a reaction temperature of 650℃,the(6,5)SWNT content reaches an impressive 67.9%among all semiconducting species,exceeding the selectivity of many commercial SWNT products.Post-CVD analysis reveals that the catalyst transforms into vanadium carbide(VC),which acts as a nucleation site for SWNT growth.Molecular dynamics simulations indicate that the energy at the SWNT-VC interface and the growth kinetics of SWNTs contribute to the chirality selectivity.This research opens up possibilities for the selective synthesis of SWNTs using cost-effective early transition metals,illuminating their future applications in fields such as bioimaging.
基金Supported by the National Natural Science Foundation of China(Nos.12272056 and 11832002)。
文摘This paper investigates the active traveling wave vibration control of an elastic supported rotating porous aluminium conical shell(CS)under impact loading.Piezoelectric smart materials in the form of micro fiber composites(MFCs)are used as actuators and sensors.To this end,a metal pore truncated CS with MFCs attached to its surface is considered.Adding artificial virtual springs at two edges of the truncated CS achieves various elastic supported boundaries by changing the spring stiffness.Based on the first-order shear deformation theory(FSDT),minimum energy principle,and artificial virtual spring technology,the theoretical formulations considering the electromechanical coupling are derived.The comparison of the natural frequency of the present results with the natural frequencies reported in previous literature evaluates the accuracy of the present approach.To study the vibration control,the integral quadrature method in conjunction with the differential quadrature approximation in the length direction is used to discretize the partial differential dynamical system to form a set of ordinary differential equations.With the aid of the velocity negative feedback method,both the time history and the input control voltage on the actuator are demonstrated to present the effects of velocity feedback gain,pore distribution type,semi-vertex angle,impact loading,and rotational angular velocity on the traveling wave vibration control.
基金China Postdoctoral Science Foundation (2023M733451)Dalian Innovation Team in Key Areas(2020RT06)Engineering Research Center for Key Aromatic Compounds and LiaoNing Key Laboratory,Liaoning Provincial Natural Science Foundation (Doctoral Research Start-up Fund 2024-BSBA-37)。
文摘Selective hydrogenation of furfural to furfuryl alcohol is a great challenge in the hydrogenation field due to thermodynamic preference for hydrogenation of C=C over C=O.Herein,a novel Al_(2)O_(3)/C-u hybrid catalyst,composed of N-modified dendritic carbon networks supporting Al_(2)O_(3)nanoparticles,was successfully prepared via carbonizing the freeze-dried gel from spontaneous cross-linking of alginate,Al3+and urea.The obtained carbon-supported Al_(2)O_(3)hybrid catalyst has a high ratio (31%) of Al species in pentahedral-coordinated state.The introduction of urea enhances the surface N content,the ratio of pyrrolic N,and specific surface area of catalyst,leading to improved adsorption capacity of C=O and the accessibility of active sites.In the furfural hydrogenation reaction with isopropyl alcohol as hydrogen donor,Al_(2)O_(3)/C-u catalyst achieved a 90%conversion of furfural with 98.0% selectivity to furfuryl alcohol,outperforming that of commercial γ-Al_(2)O_(3).Moreover,Al_(2)O_(3)/C-u demonstrates excellent catalytic stability in the recycling tests attributed to the synergistic effect of abundant weak Lewis acid sites and the anchoring effect of the carbon network on Al_(2)O_(3)nanoparticles.This work provides an innovative and facile strategy for fabrication of carbon-supported Al_(2)O_(3)hybrid catalysts with rich AlVspecies,serving as a high selective hydrogenation catalyst through MPV reaction route.
基金supported by the Technology Innovation Program(No.20026415,Development of Membrane Electrode Assembly and Stack Components for PEM Water Electrolysis)funded by the Ministry of Trade,Industry&Energy(MOTIE,Korea)supported by the National Research Foundation of Korea(NRF)grant funded by the Korean government(MSIT)(No.2022M3H4A3A01083536).
文摘The imperative demand for energy paradigm shift toward renewable and sustainable energy sources has intensified interest in proton exchange membrane water electrolysis(PEMWE)as a clean and efficient hydrogen production technology.However,the practical application of PEMWE is hindered by the scarcity and high cost of iridium(Ir),the state-of-the-art electrocatalyst for the oxygen evolution reaction(OER).To reduce Ir loading without compromising performance,we report a novel hollow Bi_(2)Te_(3)(h-Bi_(2)Te_(3))nanowire as a conductive and acid-tolerant support for Ir-based OER electrocatalysts.The h-Bi_(2)Te_(3) nanowires were synthesized via a two-step wet chemical synthesis involving Te nanowire growth and subsequent Bi incorporation,with controlled hollowness induced by modulating the reducing agent concentration.Ir nanoparticles were uniformly deposited onto h-Bi_(2)Te_(3) via polyol method,forming amorphous and well-dispersed Ir catalytic layers.Ir/h-Bi_(2)Te_(3) catalyst achieved an outstanding OER overpotential of 268 mV at 10 mA/cm^(2),a mass activity of 460 mA/mgIr at 1.55 V(vs.reversible hydrogen electrode(RHE)),and superior stability over 5 h,surpassing commercial IrO_(x)/TiO_(2),commercial Ir black,and Ir/Te benchmarks.The enhanced performance was attributed to the strong metal-support interaction,improved charge transfer,and enlarged electrochemically active surface area.Moreover,Ir/h-Bi_(2)Te_(3) catalyst demonstrated outstanding single-cell performance of 1.811 V at 2.0 A/cm^(2) with extremely low Ir loading(0.1 mgIr/cm^(2))and long-term durability(a cell voltage increase of 36.6 mV during 100 h at 1.0 A/cm^(2)),confirming its strong potential as a practical anode electrocatalyst for PEMWE.This study highlights the promise of morphology-engineered h-Bi_(2)Te_(3) supports for advancing cost-effective and durable PEMWE systems.
基金supported by the National Key R&D Program of China (No.2017YFC0210303).
文摘The expandable graphite(EG)modified TiO_(2) nanocomposites were prepared by the high shearmethod using the TiO_(2) nanoparticles(NPs)and EG as precursors,in which the amount of EG doped in TiO_(2) was 10 wt.%.Followed by the impregnation method,adjusting the pH of the solution to 10,and using the electrostatic adsorption to achieve spatial confinement,the Pt elementswere mainly distributed on the exposed TiO_(2),thus generating the Pt/10EG-TiO_(2)-10 catalyst.The best CO oxidation activity with the excellent resistance to H_(2)O and SO_(2) was obtained over the Pt/10EG-TiO_(2)-10 catalyst:CO conversion after 36 hr of the reaction was ca.85%under the harsh condition of 10 vol.%H_(2)O and 100 ppm SO_(2) at a high gaseous hourly space velocity(GHSV)of 400,000 hr−1.Physicochemical properties of the catalystswere characterized by various techniques.The results showed that the electrostatic adsorption,which riveted the Pt elements mainly on the exposed TiO_(2) of the support surface,reduced the dispersion of Pt NPs on EG and achieved the effective dispersion of Pt NPs,hence significantly improving CO oxidation activity over the Pt/10EG-TiO_(2)-10 catalyst.The 10 wt.%EG doped in TiO_(2) caused the TiO_(2) support to form a more hydrophobic surface,which reduced the adsorption of H_(2)O and SO_(2) on the catalyst,greatly inhibited deposition of the TiOSO_(4) and formation of the PtSO4 species as well as suppressed the oxidation of SO_(2),thus resulting in an improvement in the resistance to H_(2)O and SO_(2) of the Pt/10EG-TiO_(2)-10 catalyst.
基金supported by Beijing Natural Science Foundation(No.8244060)China Postdoctoral Science Foundation(No.2023M730143)+3 种基金the National Natural Science Foundation of China(No.22425601)the National Key R&D Program of China(No.2023YFB3810801)Beijing Nova Program(No.20240484659)the R&D Program of Beijing Municipal Education Commission(No.KZ202210005011).
文摘Volatile organic compounds(VOCs)exhausted from industrial processes are the major atmospheric pollutants,which could destroy the ecological environment and make hazards to human health seriously.Catalytic oxidation is regarded as the most competitive strategy for the efficient elimination of low-concentration VOCs.Supported noble metal catalysts are preferred catalysts due to their excellent low-temperature catalytic activity.To further lower the cost of catalysts,single atom catalysts(SAC)have been fabricated and extensively studied for application in VOCs oxidation due to their 100%atom-utilization efficiency and unique catalytic performance.In this review,we comprehensively summarize the recent advances in supported noble metal(e.g.,Pt,Pd,Au,and Ag)catalysts and SAC for VOCs oxidation since 2015.Firstly,this paper focuses on some important influencing factors that affect the activity of supported noble metal catalysts,including particle size,valence state and dispersion of noble metals,properties of the support,metal oxide/ion modification,preparation method,and pretreatment conditions of catalysts.Secondly,we briefly summarize the catalytic performance of SAC for typical VOCs.Finally,we conclude the key influencing factors and provide the prospects and challenges of VOCs oxidation.
基金Supported by the Outstanding Personality Innovation Funds of Henan Province(No.0121001900).
文摘Molybdenum (VI) complex, namely molybdenum dioxobis(2,4-pentanedione) [MoO2(acac)2] used as epoxidation catalyst species, was synthesized and characterized by elemental analysis and infrared spectrum. Polystyrene-supported molybdenum dioxobis(2,4-pentanedione) [MoO2(acac)2] for synthesis of epoxycyclohexane was prepared by phase transfer catalysis method. Effects of various factors in synthesis of epoxycyclohexane by reaction of cyclohexene and t-BuOOH in the atmosphere of nitrogen catalyzed by polystyrene-supported MoO2(acac)2 were also investigated. Under the following conditions, n(cyclohexene):n(t-BuOOH)=3.5:l (based on 0.1 mol of t-BuOOH), volume of solvent -10ml, reaction temperature -80℃, reaction time -60min, and mass of molybdenum in the catalyst -2.30×0^(-3)g, the yield of epoxycyclohexane on the basis of t-BuOOH is over 99.5%, and the purity of epoxycyclohexane is about 99.9% by gas chromatogram(GC) analysis.
