Obtaining the sulfonamides(SAs)concentrations in the water body and sediment bulk was a prerequisite to reveal their transport and partitioning behavior in sediment-water environments and accurately assess their ecolo...Obtaining the sulfonamides(SAs)concentrations in the water body and sediment bulk was a prerequisite to reveal their transport and partitioning behavior in sediment-water environments and accurately assess their ecological risk.In the present study,the influences of multifactor interactions on the performance of o-DGTs with XAD-18 binding gels were analyzed by central combination experiments and response surfaces analysis,in which the target compounds were 9 SAs.The results indicated that dissolved organic matter(DOM),pH,and suspended particulate matter(SS)had significant effects on the o-DGT sampling,whereas this o-DGT was independent of the ionic strength(IS).Concentning the composite influence of the four factors,the interaction between DOM and SS posed the most significant effect on all 9 SAs compounds.Subsequently,an o-DGT and DIFSmodel was applied to explore the SAs migration between the water-sediments interface.The difference between desorption rate(k_(b))and adsorption rates(k_(f))values suggested that the kinetics of SAs was dominated by adsorption.Moreover,the short-term sediment-water partitioning of SAs was clarified on the basis of distribution coefficient(K_(dl))for the labile SAs,among which the sulfadiazine(SDZ)had the largest labile pool.The ability of sediments to release SAs to the liquid phase as a sink was determined by response time(T_(c)).Among the 9 SAs,the longterm release of soseulfamethoxypyridazine(SMP)from the solid phase of sediments would have a potential risk to the aquatic environment,to which more attention should be paid in the future.展开更多
Polymeric materials,known for their lightweight and strength,are widely used today.However,their non-biodegradable nature poses significant environmental challenges.This research aimed to develop biodegradable films f...Polymeric materials,known for their lightweight and strength,are widely used today.However,their non-biodegradable nature poses significant environmental challenges.This research aimed to develop biodegradable films from fruits and vegetables,using alginate as a binding agent.Using a completely randomized design,seven experimental sets were prepared with carrots,Kimju guava,and Namwa banana peel fibers as the primary materials and alginate as the secondary material at three levels:1.2,1.8,and 2.4 by weight.The solution technique was employed to create the samples.Upon testing mechanical and physical properties,experimental set 3,consisting of 60%guava and 1.8%alginate,emerged as the optimal ratio.This combination exhibited favorable physical properties,including a thickness of 0.26±0.02 mm,meeting the standards for food packaging films.Additionally,the tensile strength was 0.50±0.01 N/m²,and the elongation at break was 55.60±0.44%.Regarding chemical properties,the moisture content of 5.64±0.03%fell within the acceptable range for dried food.Furthermore,a 30-day soil burial test revealed that the sample from experimental set 3 exhibited the highest degradation rate.In conclusion,these findings suggest that guava can be a promising raw material for producing biodegradable plastics suitable for packaging applications.展开更多
Sodium-ion batteries(SIBs)hold great promise for large-scale energy storage in the post-lithium-ion battery era due to their high rate performance and long lifespan,although their sluggish Na^(+) transformation kineti...Sodium-ion batteries(SIBs)hold great promise for large-scale energy storage in the post-lithium-ion battery era due to their high rate performance and long lifespan,although their sluggish Na^(+) transformation kinetics still require improvement.Encouraged by the excellent electrochemical performance of titanium-based anode materials,here,we present a novel titanium vanadate@carbon(TVO@C)material as anode for SIBs.Our TVO@C material is synthesized via a facile coprecipitation method,with the following annealing process in an acetylene atomosphere.The opened ion channel and the oxygen vacancies within TVO@C facilitate the diffusion of Na^(+) ions,reducing their diffusion barrier.Thus,an ultrahigh rate of 100 A g^(-1)and long life of 10,000 cycles have been achieved.Furthermore,the TVO@C electrode exhibits stable performance,not only at room temperature,but also at temperatures as low as 20 C.The TVO@CjjNa_(3)V_(2)(PO_(4))_(3)@C full cells have also achieved stable discharge/charge for 500 cycles.It is believed that this strategy provides new insight into the development of advanced electrodes and provides a new opportunity for constructing novel high rate electrodes.展开更多
Rhizoremediation has emerged as a burgeoning approach for the removal of petroleum hydrocarbons(PHCs)from soil,with a primary emphasis on terrestrial plant systems.However,the mechanism of how soil microbiomes influen...Rhizoremediation has emerged as a burgeoning approach for the removal of petroleum hydrocarbons(PHCs)from soil,with a primary emphasis on terrestrial plant systems.However,the mechanism of how soil microbiomes influence the dissipation of PHCs within a hygrophyte planting system has yet to be fully elucidated.This work concentrated on the potential evolution of soil microbiomes and their effects on PHC dissipation within the Suaeda salsa(L.)Pall.planting system in a pot experiment.Two representative compounds,polycyclic aromatic hydrocarbons(PAHs)and n-alkanes,were used as target PHCs.The findings revealed a significant efficiency in the dissipation of PHCs in soil with Suaeda salsa cultivation,particularly with respect to n-alkanes.The high dissipation efficiency of PHCs was the synergistic result of root accumulation and microbial biodegradation.The key microbes involved in PHC dissipation were revealed,with the dominant phylum Proteobacteria and genus Salinimicrobium.The alterations in microbial diversity and abundance were closely associated with root exudation and PHC exposure.Significant differences in enzyme activities,an indicator of soil health and fertility,were observed between the rhizospheric and non-rhizospheric soils,which was attributed to root exudation.This study offers novel insights into the phytoremediation potential for Suaeda in PHC-contaminated soils and serves as a valuable scientific reference for the phytoremediation of such soils.展开更多
The Cu^(+)/Cu^(0)sites of copper-based catalysts are crucial for enhancing the production of multicarbon(C_(2+))products from electrochemical CO_(2)reduction reaction(eCO_(2)RR).However,the unstable Cu^(+)and insuffic...The Cu^(+)/Cu^(0)sites of copper-based catalysts are crucial for enhancing the production of multicarbon(C_(2+))products from electrochemical CO_(2)reduction reaction(eCO_(2)RR).However,the unstable Cu^(+)and insufficient Cu^(+)/Cu^(0)active sites lead to their limited selectivity and stability for C_(2+)production.Herein,we embedded copper oxide(CuO_(x))particles into porous nitrogen-doped carbon nanofibers(CuO_(x)@PCNF)by pyrolysis of the electrospun fiber film containing ZIF-8 and Cu_(2)O particles.The porous nitrogendoped carbon nanofibers protected and dispersed Cu^(+)species,and its micro porous structure enhanced the interaction between CuO_(x)and reactants during eCO_(2)RR.The obtained CuO_(x)@PCNF created more effective and stable Cu^(+)/Cu^(0)active sites.It showed a high Faradaic efficiency of 62.5%for C_(2+)products in Hcell,which was 2 times higher than that of bare CuO_(x)(~31.1%).Furthermore,it achieved a maximum Faradaic efficiency of 80.7%for C_(2+)products in flow cell.In situ characterization and density functional theory(DFT)calculation confirmed that the N-doped carbon layer protected Cu^(+)from electrochemical reduction and lowered the energy barrier for the dimerization of^(*)CO.Stable and exposed Cu^(+)/Cu^(0)active sites enhanced the enrichment of^(*)CO and promoted the C-C coupling reaction on the catalyst surface,which facilitated the formation of C_(2+)products.展开更多
In sulfidic anoxic environments,iron sulfides are widespread solid phases that play an important role in the arsenic(As)biogeochemical cycle.This work investigated the transformation process of FeS-As coprecipitates,t...In sulfidic anoxic environments,iron sulfides are widespread solid phases that play an important role in the arsenic(As)biogeochemical cycle.This work investigated the transformation process of FeS-As coprecipitates,the concurrent behavior,and the speciation of associated As under anoxic conditions.The results showed that FeS-As coprecipitates could convert to greigite and pyrite.The transformation degree of the produced solid phases was dependent upon the pH conditions and initial As species.These results showed that the As mobilization was closely associated with the solid phase transformation.The solid phase transformationwent from disordered mackinawite to crystallinemackinawite,then greigite and finally pyrite.The As in the coprecipitates underwent a process of release,fixation,and release again.Both reduction of As(Ⅴ)and oxidation of As(Ⅲ)were observed in the aqueous and solid phases during reactions.Our study may have important implications for further understanding of As behavior and Fe/S cycling thatmay occur under an anoxic environment more comprehensively.展开更多
Particulate levoglucosan is an important tracer for biomass burning emission in ambient air.However,recent studies question its reliability as a biomass burning tracer in Chinesemega cities due to important contributi...Particulate levoglucosan is an important tracer for biomass burning emission in ambient air.However,recent studies question its reliability as a biomass burning tracer in Chinesemega cities due to important contribution from potential non-biomass burning sources,such as cooking.To address this,we examined the dynamic variation and sources of levoglucosan using a chemical ionization mass spectrometer and other advanced instruments during Beijing’s summer of 2021.The average mass concentration of levoglucosan and its isomer(C_(6)H_(10)O_(5))was 0.025±0.014μg/m^(3),constituting 0.55%±0.32%of total organic carbon(OC)in this campaign.Despite cooking emissions contributing significantly to the organic aerosol(OA,20%),levoglucosan and its isomers correlated more strongly with biomass-burning related tracers(R>0.6),black carbon(R=0.72)and less so with cooking-related sources(R=0.3).This indicates that levoglucosan is primarily dominated by biomass-burning emissions rather than cooking in Beijing’s urban areas during summertime.The diurnal variation of levoglucosan concentrations highlighted the importance of daytime and nocturnal biomass burning emissions during polluted periods in Beijing.Using levoglucosan as a tracer to quantify the biomass burning OC(BBOC),we found good agreement on the time series of BBOC between the tracermethod and other independent source apportionmentmethod.This reaffirms the reliability of levoglucosan as a biomass burning tracer.Biomass burning contributed an average of 7%-8%to OC,highlighting its significant impact on Beijing’s summer air quality.Our study enhances understanding of biomass burning influences on ambient aerosol in typical urban areas.展开更多
Pedogenic carbonates, found extensively in arid and semiarid regions, are important in revealing regional climatic and environmental changes as well as the carbon cycle. In addition, stable carbon and oxygen isotopic ...Pedogenic carbonates, found extensively in arid and semiarid regions, are important in revealing regional climatic and environmental changes as well as the carbon cycle. In addition, stable carbon and oxygen isotopic compositions of pedogenic carbonates have been used to rebuild paleoecology (biomass and vegetation) and to estimate paleotemperature and paleoprecipitation during past geological time. By utilizing the stable carbon and oxygen isotopic compositions (δ13C and (δ18O) of secondary nodules in Ustic Vertisols, this study looked into the climatic and environmental changes in the dry valleys of the Yuanmou Basin, Yunnan Province, in southwestern China. The results showed that during the early Holocene, a warm-humid or hot-humid climate existed in the Yuanmou Basin, but since then fluctuations in climate have occurred, with a dry climate prevailing. A highly significant correlation (r = 0.92, n = 9) between δ13C and δ18O values of carbonates illustrated that there had been a continual shifting between cold-humid and warm-dry climates in southwestern China including the Yuanmou Basin since the early Holocene.展开更多
The bottom ash and fly ash from the co-combustion of wood residues and peat at a bubbling fluidised bed boiler（296 MW） contained only quartz（SiO_2）, microcline（KAl Si_3O_8） and albite（NaAlSi_3O_8）. Thus, X-ray...The bottom ash and fly ash from the co-combustion of wood residues and peat at a bubbling fluidised bed boiler（296 MW） contained only quartz（SiO_2）, microcline（KAl Si_3O_8） and albite（NaAlSi_3O_8）. Thus, X-ray powder diffraction（XRD） was not useful for clarifying the difference in the release of associated heavy metals from ash matrices. In order to assess the release of heavy metals from ashes under changing environmental conditions, they were sequentially extracted and fractionated by the BCR-procedure into acid soluble/exchangeable（CH_3COOH）, reducible（NH_2OH-HCl） and oxidizable（H_2O_2/CH_3COONH_4） phases. The CH_3 COOH extractable fraction in conjunction with the total heavy metals concentrations were used to calculate the risk assessment code values for heavy metals leaching from the ash matrix. The leaching studies indicate that the heavy metals in the bottom ash and fly ash are bound to different fractions with different strengths. From the environmental and utilization perspectives, heavy metals in ashes posed different levels of environmental contamination risk. Only As in the bottom ash posed a very high risk. High risk metals were Cd in the bottom ash as well as As, Cd and Se in the fly ash.展开更多
With rapid economy growth,building energy consumption in China has been gradually increased.The energy consumption and indoor environmental quality of 51 office buildings in Hainan Province,a hot and humid area,were s...With rapid economy growth,building energy consumption in China has been gradually increased.The energy consumption and indoor environmental quality of 51 office buildings in Hainan Province,a hot and humid area,were studied through collection of verified data in site visits and field tests.The result revealed that,electricity accounted for 99.79% of the total energy consumption,natural gas 0.17%,and diesel 0.04%.The air conditioning dominated the energy use with a share of 43.18%,equipment in the particular areas 26.90%,equipment in the office rooms 11.95%,lighting system 8.67%,general service system 7.57%,and miscellaneous items 1.73%.Statistical method including six indicators obtained the energy consumption benchmark with upper limit of 98.31 kW-h/m2 and lower limit of 55.26 kW-h/m2.According to ASHRAE standard(comfortable standard) and GB/T 18883-2002(acceptable standard),the indoor environmental quality of 51 sampled office buildings was classified into three ranks:good,normal and bad.With benchmark of building energy consumption combined with indoor environmental quality,it was found that only 3.92% of sampled buildings can be identified as the best performance buildings with low energy consumption and advanced indoor environmental quality,and the buildings classified into normal level accounted for the maximum ratio.展开更多
The fructose-to-furfural transformation is facing major challenges in the selectivity and high efficiency. Herein, we have developed a simple and effective approach for the selective conversion of fructose to furfural...The fructose-to-furfural transformation is facing major challenges in the selectivity and high efficiency. Herein, we have developed a simple and effective approach for the selective conversion of fructose to furfural using Hβ zeolite modified by organic acids for dealuminization to regulate its textural and acidic properties. It was found that citric acid-dealuminized Hβ zeolite possessed high specific surface areas, wide channels and high Brønsted acid amount, which facilitated the selective conversion of fructose to furfural with a maximum yield of 76.2% at433 K for 1 h in the γ-butyrolactone(GBL)-H_(2)O system, as well as the concomitant formation of 83.0% formic acid. The^(13)C-isotope labelling experiments and the mechanism revealed that the selective cleavage of C1–C2 or C5–C6 bond on fructose was firstly occurred to form pentose or C5 intermediate by weak Brønsted acid, which was then dehydrated to furfural by strong Brønsted acid. Also this dealuminized Hβ catalyst showed the great recycling performance and was active for the conversion of glucose and mannose.展开更多
The complex air pollution driven by both Ozone(O_(3))and fine particulate matter(PM2.5)sig nificantly influences the air quality in the Sichuan Basin(SCB).Understanding the O_(3)for mation during autumn and winter is ...The complex air pollution driven by both Ozone(O_(3))and fine particulate matter(PM2.5)sig nificantly influences the air quality in the Sichuan Basin(SCB).Understanding the O_(3)for mation during autumn and winter is necessary to understand the atmospheric oxidative capacity.Therefore,continuous in-site field observations were carried out during the late summer,early autumn and winter of 2020 in a rural area of Chongqing.The total volatile organic compounds(VOCs)concentration reported by a Proton-Transfer-Reaction Time-of Flight Mass Spectrometry(PTR-ToF-MS)were 13.66±9.75 ppb,5.50±2.64 ppb,and 9.41±5.11 ppb in late summer,early autumn and winter,respectively.The anthropogenic VOCs(AVOCs)and biogenic VOCs(BVOCs)were 8.48±7.92 ppb and 5.18±2.99 ppb in late sum mer,3.31±1.89 ppb and 2.19±0.93 ppb in autumn,and 6.22±3.99 ppb and 3.20±1.27ppb in winter.A zero-dimensional atmospheric box model was employed to investigate the sensitivity of O_(3)-precursors by relative incremental reactivity(RIR).The RIR values of AV OCs,BVOCs,carbon monoxide(CO),and nitrogen oxides(NOx)were 0.31,0.71,0.09,and-0.36 for late summer,0.24,0.59,0.22,and-0.38 for early autumn,and 0.30,0.64,0.33 and-0.70 for winter,and the results showed that the O_(3)formation of sampling area was in the VOC-limited region,and O_(3)was most sensitive to BVOCs(with highest RIR values,>0.6)This study can be helpful in understanding O_(3)formation and interpreting the secondary formation of aerosols in the winter.展开更多
Human exposure to toxic metals is on the increase especially in the developing world;this is compounded by the almost unavoidable application of the metals domestically and industrially and their implication in severa...Human exposure to toxic metals is on the increase especially in the developing world;this is compounded by the almost unavoidable application of the metals domestically and industrially and their implication in several genetic defects, aging and some chronic illnesses including Autism Spectrum Disorders (ASD). This study investigated the concentration of toxic metals (Pb and V) and micro-essential elements (Cu and Se) in children with ASD and controls in Nigeria towards establishing their possible associations with the aetiopathogenesis of ASD. Eight children clinically diagnosed by Paediatric Neurologist and Child Psychiatrist for ASD using DMS-IV and fifteen apparently healthy children (age range 2 - 12 years) were recruited as cases and controls respectively. Plasma levels of Pb, V, Cu and Se were analyzed using Induction ICP-MS. Results were analyzed using students t-test. The mean plasma lead and vanadium levels were (7.92 ± 1.30 μg/dl;1.07 ± 0.22 μg/dl) and (6.83 ± 0.72 μg/dl;2.59 ± 0.48 μg/dl) in children with ASD and in controls respectively. The result showed that blood lead level in ASD was slightly increased but not significant when compared with control (p < 0.433). On the other hand, plasma vanadium concentration in ASD was significantly reduced (1.07 ± 0.22 μg/dl) when compared with control (2.59 ± 0.48 μg/dl) (P < 0.038). Mean plasma copper was similar in all participants (1.98 ± 0.13, 2.23 ± 0.12) but selenium concentrations were significantly reduced (0.37 ± 0.05 mg/L;0.57 ± 0.02 mg/L) in ASD relative to controls respectively. Given the physiological functions of vanadium and selenium, the observed reduced levels of the two elements in children with ASD may account for the speech and other neurological dysfunctions of the brain in ASD.展开更多
The mafic enclaves from Paleoproterozoic domain are considered to be the results of large-scale crust-mantle interaction and magma mixing. In this paper, petrography, mineralogy and geochemistry were jointly used to d...The mafic enclaves from Paleoproterozoic domain are considered to be the results of large-scale crust-mantle interaction and magma mixing. In this paper, petrography, mineralogy and geochemistry were jointly used to determine the origin of the mafic enclaves and their relationship with the host granitoids of the Kan granite-gneiss complex. This study also provides new information on crust-mantle interactions. The mafic enclaves of the Kan vary in shape and size and have intermediate chemical compositions. The diagrams used show a number of similarities in the major elements (and often in the trace elements) between the mafic enclaves and the host granitoids. Geochemical show that the Kan rock are metaluminous, enriched in silica, medium to high-K calc-alkaline I-type granite. The similarities reflect a mixing of basic and acid magma. Mafic enclaves have a typical magmatic structure, which is characterized by magma mixing. The genesis of these rocks is associated with the context of subduction. They result from the mixing of a mafic magma originating from the mantle and linked to subduction, and a granitic magma (type I granite) that arises from the partial melting of the crust.展开更多
Drinking good quality water is essential for better health. It is therefore essential to assess the radiological quality of all water consumed in the District of Abidjan in order to prevent related hazards. Thus, the ...Drinking good quality water is essential for better health. It is therefore essential to assess the radiological quality of all water consumed in the District of Abidjan in order to prevent related hazards. Thus, the objective of this study was to assess the risk of cancer due to the ingestion of alpha and beta emitting radionuclides in the different types of water consumed in the region. A total of 63 water samples with 43 tap water samples, 5 bottled mineral water and 15 sachet water samples was collected and taken to GAEC laboratory for analysis. The low background Gas-less Automatic Alpha/Beta counting system (Canberra iMatic<sup>TM</sup>) was used to determine alpha and beta activity concentrations. Activity concentrations of both gross alpha and gross beta obtained in water sample were respectively lower than the WHO recommended limits of 0.1 Bq/l and 1 Bq/l. Also, the annual effective dose and total equivalent effective dose found in mineral bottled water samples were higher than in other types of water. The assessment of radiological lifetime risk has shown values of cancer risk due to ingestion alpha and beta emitters lower than recommended limit. These results indicate that there is no health hazard associated to consumption of water in the District of Abidjan.展开更多
Understanding the influence of HCl on the NH_(3)-selective catalytic reduction reaction mechanism is crucial for designing highly efficient denitrification catalysts.The formation of chlorate species on the surface of...Understanding the influence of HCl on the NH_(3)-selective catalytic reduction reaction mechanism is crucial for designing highly efficient denitrification catalysts.The formation of chlorate species on the surface of the synthesized SbCeO_(x)catalyst,induced by HCl,significantly enhances low-temperature activity,as evidenced by a 30%increase in NO conversion at 155℃.Furthermore,it improves N_(2)selectivity at high temperatures,with a notable 17%increase observed at 405℃.Both experimental results and density functional theory calculations confirm that chlorate species form at Ce sites.This formation facilitates the creation of oxygen vacancies,boosting the oxygen exchange capacity.It also increases NH_(3)adsorption at the Ce sites,promotes the formation of Sb-OH,and reduces competitive OH adsorption on these sites.Notably,compared with the reaction mechanism without HCl,the presence of chlorate species enhances NH_(3)adsorption and activation,which is vital for subsequent catalytic reactions.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
Monolithic catalysts with excellent O_(3)catalytic decomposition performance were prepared by in situ loading of Co-doped KMn_(8)O_(16)on the surface of nickel foam.The triple-layer structure with Co-doped KMn_(8)O_(1...Monolithic catalysts with excellent O_(3)catalytic decomposition performance were prepared by in situ loading of Co-doped KMn_(8)O_(16)on the surface of nickel foam.The triple-layer structure with Co-doped KMn_(8)O_(16)/Ni6MnO_(8)/Ni foam was grown spontaneously on the surface of nickel foam by tuning the molar ratio of KMnO_(4)to Co(NO_(3))_(2)·6H_(2)O precursors.Importantly,the formed Ni6MnO_(8)structure between KMn_(8)O_(16)and nickel foam during in situ synthesis process effectively protected nickel foam from further etching,which significantly enhanced the reaction stability of catalyst.The optimum amount of Co doping in KMn_(8)O_(16)was available when the molar ratio of Mn to Co species in the precursor solution was 2:1.And the Mn2Co1 catalyst had abundant oxygen vacancies and excellent hydrophobicity,thus creating outstanding O_(3)decomposition activity.The O_(3)conversion under dry conditions and relative humidity of 65%,90%over a period of 5 hr was 100%,94%and 80%with the space velocity of 28,000 hr^(−1),respectively.The in situ constructed Co-doped KMn_(8)O_(16)/Ni foam catalyst showed the advantages of low price and gradual applicability of the preparation process,which provided an opportunity for the design of monolithic catalyst for O_(3)catalytic decomposition.展开更多
Global investment in ethylene(C_(2)H_(4))production via nonpetroleum pathways is rising,highlighting its growing importance in the energy and environmental sectors.The electroreduction of carbon dioxide(CO_(2))to C_(2...Global investment in ethylene(C_(2)H_(4))production via nonpetroleum pathways is rising,highlighting its growing importance in the energy and environmental sectors.The electroreduction of carbon dioxide(CO_(2))to C_(2)H_(4) inflow cells is emerging as a promising technology with broad practical applications.Direct delivery of gaseous CO_(2) to the cathode catalyst layer overcomes mass transfer limitations,enhancing reaction rates and enabling high current density.This review summarizes recent research progress in the electrocatalytic CO_(2) reduction reaction(eCO_(2)RR)for selective C_(2)H_(4) production inflow cells.It outlines the principles of eCO_(2)RR to C_(2)H_(4) and discusses the influence of copper-based catalyst morphology,crystal facet,oxidation state,surface modification strategy,and synergistic effects on catalytic performance.In addition,it highlights the compositional structure of theflow cell,and the selection and optimization of operating conditions,including gas diffusion electrodes,electrolytes,ion exchange membranes,and alternative anode reaction types beyond the oxygen evolution reaction.Finally,advances in machine learning are presented for accelerating catalyst screening and predicting dynamic changes in catalysts during reduction.This comprehensive review serves as a valuable reference for the development of efficient catalysts and the construction of electrolytic devices for the electrocatalytic reduction of CO_(2) to C_(2)H_(4).展开更多
Although the Haber–Bosch process supports the growth of modern agriculture with abundant ammonia and fertilizer production,substantial energy consumption and enormous greenhouse emissions demand an alternative and su...Although the Haber–Bosch process supports the growth of modern agriculture with abundant ammonia and fertilizer production,substantial energy consumption and enormous greenhouse emissions demand an alternative and sustainable approach.Here,we report a novel approach that combines the nonphotosynthetic bacterium Shewanella oneidensis MR-1(S.oneidensis MR-1)with cadmium sulfide(CdS)nanoparticles(NPs)to enable the photosynthesis of ammonium(NH_(4)+)from nitrate(NO_(3)^(-))using photoexcited electrons as donors.The NO_(3)^(-)reduction efficiency reached almost 100%,with an NH_(4)^(+)production selectivity of over 90%.The maximum instantaneous quantum efficiency was 3.01%under light irradiation.The reverse metal-reducing(Mtr)pathway is responsible for the transfer of photoexcited electrons to intracellular compartments.Parallel reaction monitoring analysis illustrated that NO_(3)^(-)to NH_(4)^(+)was produced via the dissimilatory nitrate reduction to ammonium(DNRA)pathway in S.oneidensis MR-1.This study provides a facile strategy for light-driven ambient NH4+synthesis and solar-to-chemical conversion.展开更多
基金supported by the National Natural Science Foundation of China(Nos.21976045 and 22076112)the CAS Key Laboratory of Coastal Environmental Processes and Ecological Remediation(No.2020KFJJ03).
文摘Obtaining the sulfonamides(SAs)concentrations in the water body and sediment bulk was a prerequisite to reveal their transport and partitioning behavior in sediment-water environments and accurately assess their ecological risk.In the present study,the influences of multifactor interactions on the performance of o-DGTs with XAD-18 binding gels were analyzed by central combination experiments and response surfaces analysis,in which the target compounds were 9 SAs.The results indicated that dissolved organic matter(DOM),pH,and suspended particulate matter(SS)had significant effects on the o-DGT sampling,whereas this o-DGT was independent of the ionic strength(IS).Concentning the composite influence of the four factors,the interaction between DOM and SS posed the most significant effect on all 9 SAs compounds.Subsequently,an o-DGT and DIFSmodel was applied to explore the SAs migration between the water-sediments interface.The difference between desorption rate(k_(b))and adsorption rates(k_(f))values suggested that the kinetics of SAs was dominated by adsorption.Moreover,the short-term sediment-water partitioning of SAs was clarified on the basis of distribution coefficient(K_(dl))for the labile SAs,among which the sulfadiazine(SDZ)had the largest labile pool.The ability of sediments to release SAs to the liquid phase as a sink was determined by response time(T_(c)).Among the 9 SAs,the longterm release of soseulfamethoxypyridazine(SMP)from the solid phase of sediments would have a potential risk to the aquatic environment,to which more attention should be paid in the future.
基金funding from the Environmental Science Program for Academic Excellence and Community Research for Fiscal Year 2024,a financial resource of the Environmental Science and Technology Program,Faculty of Science,Buriram Rajabhat University.Additionally,Buriram Rajabhat University provided a publication budget.
文摘Polymeric materials,known for their lightweight and strength,are widely used today.However,their non-biodegradable nature poses significant environmental challenges.This research aimed to develop biodegradable films from fruits and vegetables,using alginate as a binding agent.Using a completely randomized design,seven experimental sets were prepared with carrots,Kimju guava,and Namwa banana peel fibers as the primary materials and alginate as the secondary material at three levels:1.2,1.8,and 2.4 by weight.The solution technique was employed to create the samples.Upon testing mechanical and physical properties,experimental set 3,consisting of 60%guava and 1.8%alginate,emerged as the optimal ratio.This combination exhibited favorable physical properties,including a thickness of 0.26±0.02 mm,meeting the standards for food packaging films.Additionally,the tensile strength was 0.50±0.01 N/m²,and the elongation at break was 55.60±0.44%.Regarding chemical properties,the moisture content of 5.64±0.03%fell within the acceptable range for dried food.Furthermore,a 30-day soil burial test revealed that the sample from experimental set 3 exhibited the highest degradation rate.In conclusion,these findings suggest that guava can be a promising raw material for producing biodegradable plastics suitable for packaging applications.
基金supported by National Nature Science Foundation of China(22105118)Nature Science Foundation of Shandong Provinces(ZR2021QB095)China Postdoctoral Science Foundation(2020TQ0183 and 2021M701979).
文摘Sodium-ion batteries(SIBs)hold great promise for large-scale energy storage in the post-lithium-ion battery era due to their high rate performance and long lifespan,although their sluggish Na^(+) transformation kinetics still require improvement.Encouraged by the excellent electrochemical performance of titanium-based anode materials,here,we present a novel titanium vanadate@carbon(TVO@C)material as anode for SIBs.Our TVO@C material is synthesized via a facile coprecipitation method,with the following annealing process in an acetylene atomosphere.The opened ion channel and the oxygen vacancies within TVO@C facilitate the diffusion of Na^(+) ions,reducing their diffusion barrier.Thus,an ultrahigh rate of 100 A g^(-1)and long life of 10,000 cycles have been achieved.Furthermore,the TVO@C electrode exhibits stable performance,not only at room temperature,but also at temperatures as low as 20 C.The TVO@CjjNa_(3)V_(2)(PO_(4))_(3)@C full cells have also achieved stable discharge/charge for 500 cycles.It is believed that this strategy provides new insight into the development of advanced electrodes and provides a new opportunity for constructing novel high rate electrodes.
基金financially supported by the National Natural Science Foundation of China(Nos.22176025 and 22136007)the National Key Research and Development Program of China(No.2022YFC3701404)the Petro China Innovation Foundation(No.D2019-5007-0502)。
文摘Rhizoremediation has emerged as a burgeoning approach for the removal of petroleum hydrocarbons(PHCs)from soil,with a primary emphasis on terrestrial plant systems.However,the mechanism of how soil microbiomes influence the dissipation of PHCs within a hygrophyte planting system has yet to be fully elucidated.This work concentrated on the potential evolution of soil microbiomes and their effects on PHC dissipation within the Suaeda salsa(L.)Pall.planting system in a pot experiment.Two representative compounds,polycyclic aromatic hydrocarbons(PAHs)and n-alkanes,were used as target PHCs.The findings revealed a significant efficiency in the dissipation of PHCs in soil with Suaeda salsa cultivation,particularly with respect to n-alkanes.The high dissipation efficiency of PHCs was the synergistic result of root accumulation and microbial biodegradation.The key microbes involved in PHC dissipation were revealed,with the dominant phylum Proteobacteria and genus Salinimicrobium.The alterations in microbial diversity and abundance were closely associated with root exudation and PHC exposure.Significant differences in enzyme activities,an indicator of soil health and fertility,were observed between the rhizospheric and non-rhizospheric soils,which was attributed to root exudation.This study offers novel insights into the phytoremediation potential for Suaeda in PHC-contaminated soils and serves as a valuable scientific reference for the phytoremediation of such soils.
基金supported by the National Natural Science Foundation of China(22222601 and 22076019)the Fundamental Research Funds for the Central Universities(DUT23LAB611).
文摘The Cu^(+)/Cu^(0)sites of copper-based catalysts are crucial for enhancing the production of multicarbon(C_(2+))products from electrochemical CO_(2)reduction reaction(eCO_(2)RR).However,the unstable Cu^(+)and insufficient Cu^(+)/Cu^(0)active sites lead to their limited selectivity and stability for C_(2+)production.Herein,we embedded copper oxide(CuO_(x))particles into porous nitrogen-doped carbon nanofibers(CuO_(x)@PCNF)by pyrolysis of the electrospun fiber film containing ZIF-8 and Cu_(2)O particles.The porous nitrogendoped carbon nanofibers protected and dispersed Cu^(+)species,and its micro porous structure enhanced the interaction between CuO_(x)and reactants during eCO_(2)RR.The obtained CuO_(x)@PCNF created more effective and stable Cu^(+)/Cu^(0)active sites.It showed a high Faradaic efficiency of 62.5%for C_(2+)products in Hcell,which was 2 times higher than that of bare CuO_(x)(~31.1%).Furthermore,it achieved a maximum Faradaic efficiency of 80.7%for C_(2+)products in flow cell.In situ characterization and density functional theory(DFT)calculation confirmed that the N-doped carbon layer protected Cu^(+)from electrochemical reduction and lowered the energy barrier for the dimerization of^(*)CO.Stable and exposed Cu^(+)/Cu^(0)active sites enhanced the enrichment of^(*)CO and promoted the C-C coupling reaction on the catalyst surface,which facilitated the formation of C_(2+)products.
基金supported by the National Key Research and Development Program of China(No.2022YFC3701301)the National Natural Science Foundation of China(Nos.42173063 and 42377251)+1 种基金the Youth Innovation Promotion Association CAS(No.2020200)the Fundamental Research Funds for the Central Universities.
文摘In sulfidic anoxic environments,iron sulfides are widespread solid phases that play an important role in the arsenic(As)biogeochemical cycle.This work investigated the transformation process of FeS-As coprecipitates,the concurrent behavior,and the speciation of associated As under anoxic conditions.The results showed that FeS-As coprecipitates could convert to greigite and pyrite.The transformation degree of the produced solid phases was dependent upon the pH conditions and initial As species.These results showed that the As mobilization was closely associated with the solid phase transformation.The solid phase transformationwent from disordered mackinawite to crystallinemackinawite,then greigite and finally pyrite.The As in the coprecipitates underwent a process of release,fixation,and release again.Both reduction of As(Ⅴ)and oxidation of As(Ⅲ)were observed in the aqueous and solid phases during reactions.Our study may have important implications for further understanding of As behavior and Fe/S cycling thatmay occur under an anoxic environment more comprehensively.
基金supported by the National Key R&D Program of China(Nos.2022YFC3701000 and 2021YFA1601800)the National Natural Science Foundation of China(Nos.42230701 and 42375105)+1 种基金the Foundation for Program of Science and Technology Research(No.2024A1515011937)Guangdong Foundation for Program of Science and Technology Research(No.2023B1212060049).
文摘Particulate levoglucosan is an important tracer for biomass burning emission in ambient air.However,recent studies question its reliability as a biomass burning tracer in Chinesemega cities due to important contribution from potential non-biomass burning sources,such as cooking.To address this,we examined the dynamic variation and sources of levoglucosan using a chemical ionization mass spectrometer and other advanced instruments during Beijing’s summer of 2021.The average mass concentration of levoglucosan and its isomer(C_(6)H_(10)O_(5))was 0.025±0.014μg/m^(3),constituting 0.55%±0.32%of total organic carbon(OC)in this campaign.Despite cooking emissions contributing significantly to the organic aerosol(OA,20%),levoglucosan and its isomers correlated more strongly with biomass-burning related tracers(R>0.6),black carbon(R=0.72)and less so with cooking-related sources(R=0.3).This indicates that levoglucosan is primarily dominated by biomass-burning emissions rather than cooking in Beijing’s urban areas during summertime.The diurnal variation of levoglucosan concentrations highlighted the importance of daytime and nocturnal biomass burning emissions during polluted periods in Beijing.Using levoglucosan as a tracer to quantify the biomass burning OC(BBOC),we found good agreement on the time series of BBOC between the tracermethod and other independent source apportionmentmethod.This reaffirms the reliability of levoglucosan as a biomass burning tracer.Biomass burning contributed an average of 7%-8%to OC,highlighting its significant impact on Beijing’s summer air quality.Our study enhances understanding of biomass burning influences on ambient aerosol in typical urban areas.
基金Project supported by the National Key Basic Research Support Foundation of China (No. G1998040800).
文摘Pedogenic carbonates, found extensively in arid and semiarid regions, are important in revealing regional climatic and environmental changes as well as the carbon cycle. In addition, stable carbon and oxygen isotopic compositions of pedogenic carbonates have been used to rebuild paleoecology (biomass and vegetation) and to estimate paleotemperature and paleoprecipitation during past geological time. By utilizing the stable carbon and oxygen isotopic compositions (δ13C and (δ18O) of secondary nodules in Ustic Vertisols, this study looked into the climatic and environmental changes in the dry valleys of the Yuanmou Basin, Yunnan Province, in southwestern China. The results showed that during the early Holocene, a warm-humid or hot-humid climate existed in the Yuanmou Basin, but since then fluctuations in climate have occurred, with a dry climate prevailing. A highly significant correlation (r = 0.92, n = 9) between δ13C and δ18O values of carbonates illustrated that there had been a continual shifting between cold-humid and warm-dry climates in southwestern China including the Yuanmou Basin since the early Holocene.
文摘The bottom ash and fly ash from the co-combustion of wood residues and peat at a bubbling fluidised bed boiler（296 MW） contained only quartz（SiO_2）, microcline（KAl Si_3O_8） and albite（NaAlSi_3O_8）. Thus, X-ray powder diffraction（XRD） was not useful for clarifying the difference in the release of associated heavy metals from ash matrices. In order to assess the release of heavy metals from ashes under changing environmental conditions, they were sequentially extracted and fractionated by the BCR-procedure into acid soluble/exchangeable（CH_3COOH）, reducible（NH_2OH-HCl） and oxidizable（H_2O_2/CH_3COONH_4） phases. The CH_3 COOH extractable fraction in conjunction with the total heavy metals concentrations were used to calculate the risk assessment code values for heavy metals leaching from the ash matrix. The leaching studies indicate that the heavy metals in the bottom ash and fly ash are bound to different fractions with different strengths. From the environmental and utilization perspectives, heavy metals in ashes posed different levels of environmental contamination risk. Only As in the bottom ash posed a very high risk. High risk metals were Cd in the bottom ash as well as As, Cd and Se in the fly ash.
基金Project(2011BAJ01B05) supported by the National Science and Technology Pillar Program during the Twelfth Five-year Plan Period of China
文摘With rapid economy growth,building energy consumption in China has been gradually increased.The energy consumption and indoor environmental quality of 51 office buildings in Hainan Province,a hot and humid area,were studied through collection of verified data in site visits and field tests.The result revealed that,electricity accounted for 99.79% of the total energy consumption,natural gas 0.17%,and diesel 0.04%.The air conditioning dominated the energy use with a share of 43.18%,equipment in the particular areas 26.90%,equipment in the office rooms 11.95%,lighting system 8.67%,general service system 7.57%,and miscellaneous items 1.73%.Statistical method including six indicators obtained the energy consumption benchmark with upper limit of 98.31 kW-h/m2 and lower limit of 55.26 kW-h/m2.According to ASHRAE standard(comfortable standard) and GB/T 18883-2002(acceptable standard),the indoor environmental quality of 51 sampled office buildings was classified into three ranks:good,normal and bad.With benchmark of building energy consumption combined with indoor environmental quality,it was found that only 3.92% of sampled buildings can be identified as the best performance buildings with low energy consumption and advanced indoor environmental quality,and the buildings classified into normal level accounted for the maximum ratio.
基金supported by Program for National Natural Science Foundation of China(Nos.22178135,21978104 and 22278419)the National Key Research and Development Program of China(No.2021YFC2101601)。
文摘The fructose-to-furfural transformation is facing major challenges in the selectivity and high efficiency. Herein, we have developed a simple and effective approach for the selective conversion of fructose to furfural using Hβ zeolite modified by organic acids for dealuminization to regulate its textural and acidic properties. It was found that citric acid-dealuminized Hβ zeolite possessed high specific surface areas, wide channels and high Brønsted acid amount, which facilitated the selective conversion of fructose to furfural with a maximum yield of 76.2% at433 K for 1 h in the γ-butyrolactone(GBL)-H_(2)O system, as well as the concomitant formation of 83.0% formic acid. The^(13)C-isotope labelling experiments and the mechanism revealed that the selective cleavage of C1–C2 or C5–C6 bond on fructose was firstly occurred to form pentose or C5 intermediate by weak Brønsted acid, which was then dehydrated to furfural by strong Brønsted acid. Also this dealuminized Hβ catalyst showed the great recycling performance and was active for the conversion of glucose and mannose.
基金supported by the National Natural Science Foundation of China(No.42075109)the National Key Research and Development Program of China(No.2018YFC0214001)。
文摘The complex air pollution driven by both Ozone(O_(3))and fine particulate matter(PM2.5)sig nificantly influences the air quality in the Sichuan Basin(SCB).Understanding the O_(3)for mation during autumn and winter is necessary to understand the atmospheric oxidative capacity.Therefore,continuous in-site field observations were carried out during the late summer,early autumn and winter of 2020 in a rural area of Chongqing.The total volatile organic compounds(VOCs)concentration reported by a Proton-Transfer-Reaction Time-of Flight Mass Spectrometry(PTR-ToF-MS)were 13.66±9.75 ppb,5.50±2.64 ppb,and 9.41±5.11 ppb in late summer,early autumn and winter,respectively.The anthropogenic VOCs(AVOCs)and biogenic VOCs(BVOCs)were 8.48±7.92 ppb and 5.18±2.99 ppb in late sum mer,3.31±1.89 ppb and 2.19±0.93 ppb in autumn,and 6.22±3.99 ppb and 3.20±1.27ppb in winter.A zero-dimensional atmospheric box model was employed to investigate the sensitivity of O_(3)-precursors by relative incremental reactivity(RIR).The RIR values of AV OCs,BVOCs,carbon monoxide(CO),and nitrogen oxides(NOx)were 0.31,0.71,0.09,and-0.36 for late summer,0.24,0.59,0.22,and-0.38 for early autumn,and 0.30,0.64,0.33 and-0.70 for winter,and the results showed that the O_(3)formation of sampling area was in the VOC-limited region,and O_(3)was most sensitive to BVOCs(with highest RIR values,>0.6)This study can be helpful in understanding O_(3)formation and interpreting the secondary formation of aerosols in the winter.
文摘Human exposure to toxic metals is on the increase especially in the developing world;this is compounded by the almost unavoidable application of the metals domestically and industrially and their implication in several genetic defects, aging and some chronic illnesses including Autism Spectrum Disorders (ASD). This study investigated the concentration of toxic metals (Pb and V) and micro-essential elements (Cu and Se) in children with ASD and controls in Nigeria towards establishing their possible associations with the aetiopathogenesis of ASD. Eight children clinically diagnosed by Paediatric Neurologist and Child Psychiatrist for ASD using DMS-IV and fifteen apparently healthy children (age range 2 - 12 years) were recruited as cases and controls respectively. Plasma levels of Pb, V, Cu and Se were analyzed using Induction ICP-MS. Results were analyzed using students t-test. The mean plasma lead and vanadium levels were (7.92 ± 1.30 μg/dl;1.07 ± 0.22 μg/dl) and (6.83 ± 0.72 μg/dl;2.59 ± 0.48 μg/dl) in children with ASD and in controls respectively. The result showed that blood lead level in ASD was slightly increased but not significant when compared with control (p < 0.433). On the other hand, plasma vanadium concentration in ASD was significantly reduced (1.07 ± 0.22 μg/dl) when compared with control (2.59 ± 0.48 μg/dl) (P < 0.038). Mean plasma copper was similar in all participants (1.98 ± 0.13, 2.23 ± 0.12) but selenium concentrations were significantly reduced (0.37 ± 0.05 mg/L;0.57 ± 0.02 mg/L) in ASD relative to controls respectively. Given the physiological functions of vanadium and selenium, the observed reduced levels of the two elements in children with ASD may account for the speech and other neurological dysfunctions of the brain in ASD.
文摘The mafic enclaves from Paleoproterozoic domain are considered to be the results of large-scale crust-mantle interaction and magma mixing. In this paper, petrography, mineralogy and geochemistry were jointly used to determine the origin of the mafic enclaves and their relationship with the host granitoids of the Kan granite-gneiss complex. This study also provides new information on crust-mantle interactions. The mafic enclaves of the Kan vary in shape and size and have intermediate chemical compositions. The diagrams used show a number of similarities in the major elements (and often in the trace elements) between the mafic enclaves and the host granitoids. Geochemical show that the Kan rock are metaluminous, enriched in silica, medium to high-K calc-alkaline I-type granite. The similarities reflect a mixing of basic and acid magma. Mafic enclaves have a typical magmatic structure, which is characterized by magma mixing. The genesis of these rocks is associated with the context of subduction. They result from the mixing of a mafic magma originating from the mantle and linked to subduction, and a granitic magma (type I granite) that arises from the partial melting of the crust.
文摘Drinking good quality water is essential for better health. It is therefore essential to assess the radiological quality of all water consumed in the District of Abidjan in order to prevent related hazards. Thus, the objective of this study was to assess the risk of cancer due to the ingestion of alpha and beta emitting radionuclides in the different types of water consumed in the region. A total of 63 water samples with 43 tap water samples, 5 bottled mineral water and 15 sachet water samples was collected and taken to GAEC laboratory for analysis. The low background Gas-less Automatic Alpha/Beta counting system (Canberra iMatic<sup>TM</sup>) was used to determine alpha and beta activity concentrations. Activity concentrations of both gross alpha and gross beta obtained in water sample were respectively lower than the WHO recommended limits of 0.1 Bq/l and 1 Bq/l. Also, the annual effective dose and total equivalent effective dose found in mineral bottled water samples were higher than in other types of water. The assessment of radiological lifetime risk has shown values of cancer risk due to ingestion alpha and beta emitters lower than recommended limit. These results indicate that there is no health hazard associated to consumption of water in the District of Abidjan.
文摘Understanding the influence of HCl on the NH_(3)-selective catalytic reduction reaction mechanism is crucial for designing highly efficient denitrification catalysts.The formation of chlorate species on the surface of the synthesized SbCeO_(x)catalyst,induced by HCl,significantly enhances low-temperature activity,as evidenced by a 30%increase in NO conversion at 155℃.Furthermore,it improves N_(2)selectivity at high temperatures,with a notable 17%increase observed at 405℃.Both experimental results and density functional theory calculations confirm that chlorate species form at Ce sites.This formation facilitates the creation of oxygen vacancies,boosting the oxygen exchange capacity.It also increases NH_(3)adsorption at the Ce sites,promotes the formation of Sb-OH,and reduces competitive OH adsorption on these sites.Notably,compared with the reaction mechanism without HCl,the presence of chlorate species enhances NH_(3)adsorption and activation,which is vital for subsequent catalytic reactions.
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.
基金supported by the National Natural Science Foundation of China (Nos.21876019 and 22276022)the National Key Research and Development Program of China (No.2019YFC1903903).
文摘Monolithic catalysts with excellent O_(3)catalytic decomposition performance were prepared by in situ loading of Co-doped KMn_(8)O_(16)on the surface of nickel foam.The triple-layer structure with Co-doped KMn_(8)O_(16)/Ni6MnO_(8)/Ni foam was grown spontaneously on the surface of nickel foam by tuning the molar ratio of KMnO_(4)to Co(NO_(3))_(2)·6H_(2)O precursors.Importantly,the formed Ni6MnO_(8)structure between KMn_(8)O_(16)and nickel foam during in situ synthesis process effectively protected nickel foam from further etching,which significantly enhanced the reaction stability of catalyst.The optimum amount of Co doping in KMn_(8)O_(16)was available when the molar ratio of Mn to Co species in the precursor solution was 2:1.And the Mn2Co1 catalyst had abundant oxygen vacancies and excellent hydrophobicity,thus creating outstanding O_(3)decomposition activity.The O_(3)conversion under dry conditions and relative humidity of 65%,90%over a period of 5 hr was 100%,94%and 80%with the space velocity of 28,000 hr^(−1),respectively.The in situ constructed Co-doped KMn_(8)O_(16)/Ni foam catalyst showed the advantages of low price and gradual applicability of the preparation process,which provided an opportunity for the design of monolithic catalyst for O_(3)catalytic decomposition.
基金supported by the National Natural Science Foundation of China(22272081 and 51802160)the Startup Foundation for Introducing Talent of NUIST(S8113082001).
文摘Global investment in ethylene(C_(2)H_(4))production via nonpetroleum pathways is rising,highlighting its growing importance in the energy and environmental sectors.The electroreduction of carbon dioxide(CO_(2))to C_(2)H_(4) inflow cells is emerging as a promising technology with broad practical applications.Direct delivery of gaseous CO_(2) to the cathode catalyst layer overcomes mass transfer limitations,enhancing reaction rates and enabling high current density.This review summarizes recent research progress in the electrocatalytic CO_(2) reduction reaction(eCO_(2)RR)for selective C_(2)H_(4) production inflow cells.It outlines the principles of eCO_(2)RR to C_(2)H_(4) and discusses the influence of copper-based catalyst morphology,crystal facet,oxidation state,surface modification strategy,and synergistic effects on catalytic performance.In addition,it highlights the compositional structure of theflow cell,and the selection and optimization of operating conditions,including gas diffusion electrodes,electrolytes,ion exchange membranes,and alternative anode reaction types beyond the oxygen evolution reaction.Finally,advances in machine learning are presented for accelerating catalyst screening and predicting dynamic changes in catalysts during reduction.This comprehensive review serves as a valuable reference for the development of efficient catalysts and the construction of electrolytic devices for the electrocatalytic reduction of CO_(2) to C_(2)H_(4).
基金supported by the National Key Research and Development Project(2019YFA0705804).
文摘Although the Haber–Bosch process supports the growth of modern agriculture with abundant ammonia and fertilizer production,substantial energy consumption and enormous greenhouse emissions demand an alternative and sustainable approach.Here,we report a novel approach that combines the nonphotosynthetic bacterium Shewanella oneidensis MR-1(S.oneidensis MR-1)with cadmium sulfide(CdS)nanoparticles(NPs)to enable the photosynthesis of ammonium(NH_(4)+)from nitrate(NO_(3)^(-))using photoexcited electrons as donors.The NO_(3)^(-)reduction efficiency reached almost 100%,with an NH_(4)^(+)production selectivity of over 90%.The maximum instantaneous quantum efficiency was 3.01%under light irradiation.The reverse metal-reducing(Mtr)pathway is responsible for the transfer of photoexcited electrons to intracellular compartments.Parallel reaction monitoring analysis illustrated that NO_(3)^(-)to NH_(4)^(+)was produced via the dissimilatory nitrate reduction to ammonium(DNRA)pathway in S.oneidensis MR-1.This study provides a facile strategy for light-driven ambient NH4+synthesis and solar-to-chemical conversion.
