All of the experimentally known electronic states of the Cr group metal monoxides(Cr O,Mo O,and WO)have been presented in the paper.The optical spectra of the Cr O molecule have been investigated in the gas phase thro...All of the experimentally known electronic states of the Cr group metal monoxides(Cr O,Mo O,and WO)have been presented in the paper.The optical spectra of the Cr O molecule have been investigated in the gas phase through a combination of the laser-induced fluorescence(LIF)excitation and single-vibronic-level(SVL)emission spectroscopy in the supersonic expansion.The rotational constants of the vibronic electronic states,including X^(5)Π_(-1)(v=0–3),B^(5)Π_(-1)(v=0–10),and B~5Π_1(v=1,5),and the vibrational constants of the spin–orbit components X^(5)Π_(-1,0,1)have been obtained.The molecular constants of the Mo O and WO molecules have been summarized by reviewing the previous spectroscopic studies,and a comprehensive energy level diagram of the Cr group metal monoxides has been constructed.By comparing the electronic configurations,bond lengths,and vibrational frequencies of all the transition metal monoxides in the ground electronic state,the significance of the relativistic effect in the bonding of the 5d transition metal monoxides has been discussed.The related spectroscopic data of the Cr O molecule are available at https://doi.org/10.57760/sciencedb.j00113.00085.展开更多
It is challenging to diagnose isolated hyperbilirubinemia with rare and complex etiologies under the constraints of traditional testing conditions.Herein,we present a rare case of coexisting Gilbert syndrome(GS)and er...It is challenging to diagnose isolated hyperbilirubinemia with rare and complex etiologies under the constraints of traditional testing conditions.Herein,we present a rare case of coexisting Gilbert syndrome(GS)and erythropoietic protoporphyria(EPP),which has not been previously documented.CASE SUMMARY We present a rare case of coexisting GS and EPP in a 23-year-old Chinese male with a long history of jaundice and recently found splenomegaly.Serial nonspecific hemolysis screening tests yielded inconsistent results,and investigations for common hemolytic etiologies were negative.However,Levitt’s carbon monoxide breath test,which measures erythrocyte lifespan(the gold-standard marker of hemolysis),demonstrated significant hemolysis,revealing a markedly shortened erythrocyte lifespan of 11 days(normal average 120 days).Genetic testing subsequently confirmed EPP with a homozygous ferrochelatase gene mutation and GS with a heterozygous uridine diphosphate glucuronosyl trans-ferase 1A1 gene mutation.CONCLUSION The rapid,non-invasive Levitt’s carbon monoxide breath test resolved the diagnostic challenge posed by a rare and complex cause of hyperbilirubinemia.展开更多
Chiral carbonyl compounds frequently occur in natural products and pharmaceuticals. Additionally, they serve as important intermediates in organic synthesis. Transition metal-catalyzed asymmetric carbonylative cross-c...Chiral carbonyl compounds frequently occur in natural products and pharmaceuticals. Additionally, they serve as important intermediates in organic synthesis. Transition metal-catalyzed asymmetric carbonylative cross-coupling reactions are among the most straightforward and effective methods for synthesizing chiral carbonyl compounds, including esters, amides, and ketones. The advances in asymmetric carbonylative cross-coupling reactions using various O-, N-, C-, and S-containing nucleophiles or electrophiles over the past decade are summarized.展开更多
Objective:The neurotoxicity of carbon monoxide(CO)to the central nervous system is a key pathogenesis of delayed encephalopathy after acute carbon monoxide poisoning(DEACMP).Our previous study found that retinoic acid...Objective:The neurotoxicity of carbon monoxide(CO)to the central nervous system is a key pathogenesis of delayed encephalopathy after acute carbon monoxide poisoning(DEACMP).Our previous study found that retinoic acid(RA)can suppress the neurotoxic effects of CO.This study further explores,in vivo and in vitro,the molecular mechanisms by which RA alleviates CO-induced central nervous system damage.Methods:A cytotoxic model was established using the mouse hippocampal neuronal cell line HT22 and primary oligodendrocytes exposed to CO,and a DEACMP animal model was established in adult Kunming mice.Cell viability and apoptosis of hippocampal neurons and oligodendrocytes were assessed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide(MTT)assay and Annexin V/propidium iodide(PI)double staining.The transcriptional and protein expression of each gene was detected using real time fluorescence quantitative PCR(RT-qPCR)and Western blotting.Long noncoding RNA(lncRNA)SNHG15 and LINGO-1 were knocked down or overexpressed to observe changes in neurons and oligodendrocytes.In DEACMP mice,SNHG15 or LINGO-1 were knocked down to assess changes in central nervous tissue and downstream protein expression.Results:RA at 10 and 20μmol/L significantly reversed CO-induced apoptosis of hippocampal neurons and oligodendrocytes,downregulation of SNHG15 and LINGO-1,and upregulation of brain-derived neurotrophic factor(BDNF)and tyrosine kinase receptor B(TrkB)(all P<0.05).Overexpression of SNHG15 or LINGO-1 weakened the protective effect of RA against CO-induced cytotoxicity(all P<0.05).Knockdown of SNHG15 or LINGO-1 alleviated CO-induced apoptosis of hippocampal neurons and oligodendrocytes and upregulated BDNF and TrkB expression levels(all P<0.05).Experiments in DEACMP model mice showed that knockdown of SNHG15 or LINGO-1 mitigated central nervous system injury in DEACMP(all P<0.05).Conclusion:RA alleviates CO-induced apoptosis of hippocampal neurons and oligodendrocytes,thereby reducing central nervous system injury and exerting neuroprotective effects.LncRNA SNHG15 and LINGO-1 are key molecules mediating RA induced inhibition of neuronal apoptosis and are associated with the BDNF/TrkB pathway.These findings provide a theoretical framework for optimizing the clinical treatment of DEACMP and lay an experimental foundation for elucidating its molecular mechanisms.展开更多
This study systematically investigated the effects of experimental conditions,crystal phase,and microstructure on the preparation of V_(2)O_(3)for vanadium flow batteries by reducing ammonium metavanadate extracted fr...This study systematically investigated the effects of experimental conditions,crystal phase,and microstructure on the preparation of V_(2)O_(3)for vanadium flow batteries by reducing ammonium metavanadate extracted from waste catalyst.The optimized experimental conditions were determined as follows:the CO reduction temperature was set at 575℃,the reduction time was 1 hour,the CO flow rate was 50 mL/min,and furnace cooling was performed subsequently.Under these conditions,the samples obtained were predominantly composed of single-phase V_(2)O_(3).Microstructural analysis reveals tightly packed grain configurations exhibiting flake-like or block-like morphologies.Significantly,the as-synthesized V_(2)O_(3)demonstrates sufficient purity for fabricating high-performance electrolytes in all-vanadium flow batteries,showing promising electrochemical applicability.展开更多
Carbon monoxide(CO)is a crucial gaseous signaling molecule that regulates various physiological and pathological processes,and may exert an anti-inflammatory and protective role in drug-induced liver injury(DILI).Desp...Carbon monoxide(CO)is a crucial gaseous signaling molecule that regulates various physiological and pathological processes,and may exert an anti-inflammatory and protective role in drug-induced liver injury(DILI).Despite this,understanding the exact relationship between CO and the occurrence and development of DILI remains challenging.Hence,there is an urgent need to develop a reliable and robust tool for the rapid visual detection and assessment of CO in this context.Herein,we presented a novel near-infrared(NIR)fluorescent nanoprobe with aggregation-induced emission(AIE)properties and excited-state intramolecular proton transfer(ESIPT)characteristics for the detection and imaging of CO both in vitro and in vivo.Simultaneously,the nanoprobe enables self-assembly form nanoaggregates in aqueous media with high biocompatible,which can sense CO in situ through the conversion of yellowto-red fluorescence facilitated aggregation-induced dual-color fluorescence.What is more,this nanoprobe shows ratiometric respond to CO,which demonstrates excellent stability,high sensitivity(with a detection limit of 12.5 nmol/L),and superior selectivity.Crucially,this nanoprobe enables the visual detection of exogenous and endogenous CO in living cells and tissues affected by DILI,offering a user-friendly tool for real-time visualization of CO in living system.Hence,it holds great promise in advancing our understanding of CO’s role.展开更多
Cu(I)based CO adsorbents are prone to oxidation and deactivation owing to the sensitivity of Cu^(+) ions to oxygen and moisture in the humid air.In this study,in order to improve its antioxidant performance,hydrophobi...Cu(I)based CO adsorbents are prone to oxidation and deactivation owing to the sensitivity of Cu^(+) ions to oxygen and moisture in the humid air.In this study,in order to improve its antioxidant performance,hydrophobic Cu(I)based adsorbents were fabricated using polytetrafluoroethylene(PTFE)for the hydrophobic modification,effectively avoiding the contact of CuCl active species with moisture,thereby inhibiting the oxidation of the Cu(I)based adsorbents.The successful introduction of PTFE into the activated carbon(AC)carrier significantly improves the hydrophobicity of the adsorbent.The optimal adsorbent CuCl(6)@AC-PTFE(0.10%)with the CuCl loading of 6 mmol·g^(-1)and the PTFE mass concentration of 0.10%exhibits an excellent CO adsorption capacity of 3.61 mmol·g^(-1)(303 K,500 kPa)as well as high CO/CO_(2)and CO/N_(2)adsorption selectivities of 29 and 203(303 K,100 kPa).Particularly,compared with the unmodified adsorbents,the antioxidant performance of modified adsorbent CuCl(6)@AC-PTFE(0.10%)is significantly improved,holding 86%of CO adsorption performance of fresh one after 24 h of exposure to humid air with a relative humidity of 70%,making the fabricated composite a promising adsorbent for CO separation.展开更多
Single carbon products(C1 compounds) are simple but important chemicals in the road towards energy transition.Catalytic conversion of CO_(2) with H_(2)(desirably renewable) can be performed over reducible oxides suppo...Single carbon products(C1 compounds) are simple but important chemicals in the road towards energy transition.Catalytic conversion of CO_(2) with H_(2)(desirably renewable) can be performed over reducible oxides supporting transition metals to obtain products such as CH_(4),CO and MeOH.Oxygen vacancies(O-vacancies),which are inherent defects of reducible metal oxides,play an enormous role in driving the catalytic performance(activity,selectivity,stability) for the desired reactions.Yet,the assessment of O-defects at realistic conditions is often complex.Only few techniques can provide direct evidence for their existence and influence in CO_(2) activation.Among them,electron paramagnetic spectroscopy(EPR),Raman spectroscopy,scanning probe microscopies(SPM) and environmental transmission electron microscopy(ETEM) are nowadays the most informative.In most cases,however,the measurements require reaction conditions far away from CO_(2) valorization applications.Although great efforts have been fruitful in explaining and demonstrating the huge importance of O-vacancies in CO_(2) catalysis,still ambiguous or erroneous interpretations about structure-function correlations involving O-vacancies are found in literature,especially,when information is not properly gathered,e.g.,by O 1s ex-situ X-ray photon spectroscopy(XPS).Moreover,despite the recognized importance of O-vacancies for CO_(2) valorization,critical literature compilations about their effects in thermal processes are scarce.Herein,we attempt to contribute in closing this gap by integrally encompassing representative investigations on the thermo-catalytic production of CH_(4),CO and MeOH.Particularly,we emphasize on the proper selection of assessment tools(direct/indirect) to unambiguously establish structure-function relationships to design optimized O-defective catalysts for the targeted compounds.展开更多
The high hydrogen desorption density(19.6 wt%)of ammonia borane(AB)makes it one of the most promising chemical hydrogen storage materials.Developing cost-effective catalysts is the key for accelerating the hydrolysis ...The high hydrogen desorption density(19.6 wt%)of ammonia borane(AB)makes it one of the most promising chemical hydrogen storage materials.Developing cost-effective catalysts is the key for accelerating the hydrolysis of AB.Herein,we present a straightforward synthesis method for the Cu_(2)O decorated CoO catalyst derived from ZIF-67 precursors using carbothermal shock(~1 s)in air.The obtained results demonstrate that a small amount of Cu_(2)O doping into CoO synergistically enhances AB hydrolysis,resulting in an almost fivefold increase in turnover frequency(TOF=97 molH_(2)molCoO-1min-1at 298 K).Further studies indicated that the incorporation of Cu_(2)O alters the electronic distribution of the surface of catalysts,introducing more oxygen vacancies and increasing the pyridinic nitrogen content.The increased oxygen vacancies effectively enhanced the adsorption and activation ability of active sites for reactants(H_(2)O and AB),while the targeting effect of pyridinic nitrogen enhances the dispersion of the catalyst.Theoretical analysis reveals that CoO plays a key role in the dissociation of H_(2)O,while minor doping with Cu_(2)O substantially reduces the dissociation energy barrier of AB.This research provides a novel strategy for the design and efficient preparation of AB hydrolysis catalysts for efficient hydrogen production.展开更多
The electrochemical carbon dioxide reduction reaction(CO_(2)RR)can convert carbon dioxide into highvalue chemical substances and fuels by utilizing renewable electricity,which can not only complete the carbon cycle bu...The electrochemical carbon dioxide reduction reaction(CO_(2)RR)can convert carbon dioxide into highvalue chemical substances and fuels by utilizing renewable electricity,which can not only complete the carbon cycle but also effectively alleviate the problems of global warming and energy shortage.Nickelbased catalysts hold great promise and unbeatable merits for the electroreduction of carbon dioxide due to their excellent catalytic properties and activity.However,there were few review papers on the application of nickel-based catalysts in carbon dioxide electroreduction.This paper,therefore,presents the current status of research on nickel-based catalysts in carbon dioxide electroreduction categorized by different products.First,the advantages of CO_(2) electroreduction and nickel-based catalysts as well as the basic principles of CO_(2) electroreduction are presented;then the different types of nickel-based catalysts that can convert CO_(2) into different products are described in detail,including their syntheses,performances,and mechanisms.Finally,the common features of nickel-based catalysts towards different carbon dioxide electroreduction products,as well as the outlooks for the development of nickel-based catalysts will be summarized.It is highly expected that this review will help in the future research and development of nickel-based catalysts towards CO_(2) conversion.展开更多
Aerated drip irrigation(ADI)is an important practice for promoting soil fertility and crop productivity in greenhouse vegetable production,yet little research has comprehensively investigated its effects on the functi...Aerated drip irrigation(ADI)is an important practice for promoting soil fertility and crop productivity in greenhouse vegetable production,yet little research has comprehensively investigated its effects on the functional traits of carbon(C)-cycling microorganisms.In this study,we sought to assess the potential efficacy of ADI in increasing soil organic C(SOC)by changing soil microbial communities and the expressions of genes associated with C cycling.To this end,we adopted a metagenomic approach to compare the effects of ADI with three dissolved oxygen concentrations(10,15,and 20 mg L^(-1))during a three-season tomato cultivation experiment in northern China.The results revealed that the 10 mg L^(-1)treatment led to a significant increase in the abundance of korA/B genes(associated with the reductive tricarboxylic acid cycle)in the C fixation pathway,whereas the 15 mg L^(-1)treatment increased the abundances of cbbL/R and coxL/S genes associated with the Calvin cycle and carbon monoxide oxidation,respectively.In addition,based on a co-occurrence network analysis,we observed a positive correlation between cbbL and coxS.Interestingly,r-selected microorganisms,such as Proteobacteria and Actinobacteria,characterized by rapid cell multiplication and high biomass production,were identified as the primary contributors to C fixation and were the main predictors of SOC pools.In contrast,the 20 mg L^(-1)treatment was found to adversely influence C fixation,although the enhanced C degradation could be attributed to the extracellular enzymes secreted by K-selected microorganisms.Collectively,our findings indicate that ADI with dissolved oxygen concentrations 15 mg L^(-1)can promote SOC content by altering the life history strategies of r-selected microorganisms and genes associated with C fixation.These findings will provide valuable references for agroecosystem irrigation management,help improve soil fertility,and promote sustainable production.展开更多
The experiment explored the Fe_(2)O_(3) reduction process with H_(2)/CO mixed gas and confirmed a promoting effect from CO when its volume proportion in mixed gas is 20% at 850℃.The ReaxFF molecular dynamics(MD)simul...The experiment explored the Fe_(2)O_(3) reduction process with H_(2)/CO mixed gas and confirmed a promoting effect from CO when its volume proportion in mixed gas is 20% at 850℃.The ReaxFF molecular dynamics(MD)simulation method was used to observe the reduction process and provide an atomic-level explanation.The accuracy of the parameters used in the simulation was verified by the density functional theory(DFT)calculation.The simulation shows that the initial reduction rate of H_(2) is much faster than that of CO(from 800 to 950℃).As the reduction proceeds,cementite,obtained after CO participates in the reduction at 850℃,will appear on the iron surface.Due to the active properties of C atoms in cementite,they are easy to further react with the O atoms in Fe_(2)O_(3).The generation of internal CO may destroy the dense structure of the surface layer,thereby affecting the overall reduction swelling of Fe_(2)O_(3).However,excess CO is detrimental to the reaction rate,mainly because of the poor thermodynamic conditions of CO in the temperature range and the molecular diffusion capacity is not as good as that of H_(2).Furthermore,the surface structures obtained after H_(2) and CO reduction have been compared,and it was found that the structure obtained by CO reduction has a larger surface area,thus promoting the sub sequent reaction of H_(2).展开更多
The Hyperspectral Infrared Atmospheric Sounder-II(HIRAS-II)onboard China’s FungYun(FY)-3F meteorological satellite was launched in August 2023.This study presents the first attempt to retrieve the global carbon monox...The Hyperspectral Infrared Atmospheric Sounder-II(HIRAS-II)onboard China’s FungYun(FY)-3F meteorological satellite was launched in August 2023.This study presents the first attempt to retrieve the global carbon monoxide(CO)column from HIRAS-II/FY-3F spectra based on a newly established full-physics algorithm.The CO global columns derived from the HIRAS-II/FY-3F satellite are compared to measurements from the Infrared Atmospheric Sounding Interferometer(IASI)onboard Europe’s MetopB satellite,as both satellites have the same spectral range with a similar overpass time.The correlation coefficient between the IASI/Metop-B and HIRAS-II/FY-3F CO retrievals is about 0.8.The HIRAS-II/FY-3F satellite can capture well the regions with high CO values,e.g.,Africa,North America,and East Asia.The relative difference in the CO global column between HIRAS-II and IASI is 1.2±13.7(1)%,which is within their combined retrieval uncertainty.The CO plumes from the fire emissions in North America between 18 and 23 July 2024 were observed by the HIRAS-II/FY-3F satellite and consistent with the CAMS(Copernicus Atmosphere Monitoring Service)model simulations.Our results show that the HIRAS-II/FY-3F spectra are of good enough quality to provide quantitative observations of global CO column remote sensing observations.展开更多
Jet ventilation is widely used in the ventilation design of highway and railway tunnels as an important air supply method during tunnel operation and disaster periods.This ventilation method has also been applied for ...Jet ventilation is widely used in the ventilation design of highway and railway tunnels as an important air supply method during tunnel operation and disaster periods.This ventilation method has also been applied for fire control in immersed tunnels.We conduct numerical simulations using computational fluid dynamics(CFD)to study positive ventilation in the upstream and reverse ventilation in the downstream(P-R)for an extra-wide immersed tunnel.The effects of fire source location and jet fan air velocity response strategy on the ceiling temperature decay,carbon monoxide(CO)distribution,and smoke exhaust efficiency were investigated for varying fire source locations.The results show that flames will be tilted to the side of the jet fan with a smaller air velocity.Additionally,the jet fan air velocity should be adjusted based on the relative distance between the fire source and the smoke vent.Among the studied scenarios,the most effective outcome was achieved when the air velocity was adjusted to 25 m/s on the side near the smoke vent.Also in this scenario,the phenomenon of smoke deposition was effectively mitigated and the average smoke exhaust efficiency reached 87%.Moreover,we found that the temperature decay of the tunnel follows an exponential decay law.The temperature decay rate is significantly higher on the side closest to the smoke vent compared to the farther side.This research provides a theoretical basis for smoke control strategies for fires that occur in immersed tunnels.展开更多
In this work,the incorporation of tantalum(Ta)into p-type metal-oxide(SnO_(x))semiconductor film is investigated to improve the electrical characteristics and suppress the fringe effect of thin film transistors(TFTs)....In this work,the incorporation of tantalum(Ta)into p-type metal-oxide(SnO_(x))semiconductor film is investigated to improve the electrical characteristics and suppress the fringe effect of thin film transistors(TFTs).The Ta-doped SnO_(x)(SnO_(x):Ta)film is deposited by radio-frequency(RF)magnetron sputtering with a Sn:Ta(3 at.%)target and thermally annealed at 270℃ for 30 min.Here,we observe that the SnO_(x):Ta film presents increased crystallinity,reduced defect density(3.25×10^(12)cm^(−2)·eV^(−1)),and widened bandgap(1.98 eV),in comparison with the undoped SnO_(x)film.As a result,the SnO_(x):Ta TFTs exhibit a lower off-state current(Ioff),an improved on/off current ratio(2.17×10^(4)),a remarkably decreased subthreshold swing(SS)by 41%,and enhanced device stability.Additionally,by introducing Ta dopants,the fringe effect as well as the impact of channel width-to-length ratio(W/L)on electrical performances of the p-type oxide TFTs can be effectively suppressed.These results shall contribute to further exploration and development of p-type SnO_(x)TFTs.展开更多
To develop efficient catalysts for ambient carbon monoxide(CO)oxidation is significant for indoor air purification and also for many industrial applications.In this work,the catalytic activity for CO oxidation were en...To develop efficient catalysts for ambient carbon monoxide(CO)oxidation is significant for indoor air purification and also for many industrial applications.In this work,the catalytic activity for CO oxidation were enhanced by tuning the metal-support interaction of Ru/CeO_(2)catalysts.A series of Ru/CeO_(2)catalysts were synthesized by an impregnation method with calcination at 100,200,400 and 600℃,respectively,to regulate the Ru-CeO_(2)interaction.We discovered that low temperature calcination(100℃)induced more Ru-O-Ce bonds and stronger Ru-CeO_(2)interaction,while high temperature calcination(≥400℃)caused the agglomeration of Ru species with more Ru-O-Ru bonds and weaker Ru-CeO_(2)interaction,resulting in the lower redox capacity of these catalysts,as well as lower catalytic activity for CO oxidation.Only calcination at moderate 200℃ can induce the moderate interaction between Ru species and CeO_(2)support,which can keep the high dispersion of RuO_(x)species with the high redox capacity,thus leading to complete elimination of 500 ppm CO at room temperature on Ru/Ce-200 catalyst.展开更多
The structure and catalytic desulfurization characteristics of CeO2-TiO2 mixed oxides were investigated by means ofX-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and catalytic activity tests. Acco...The structure and catalytic desulfurization characteristics of CeO2-TiO2 mixed oxides were investigated by means ofX-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and catalytic activity tests. According to the results, a CeO2-TiO2solid solution is formed when the mole ratio of cerium to titanium n（Ce）：n（Ti） is 5：5 or greater, and the most suitable n（Ce）：n（Ti） isdetermined as 7：3, over which the conversion rate of SO2 and the yield of sulfur at 500℃ reach 93% and 99%, respectively.According to the activity testing curve, Ce0.7Ti0.3O2 （n（Ce）：n（Ti）=7：3） without any pretreatment can be gradually activated by reagentgas after about 10 min, and reaches a steady activation status 60 min later. The XPS results of Ce0.7Ti0.3O2 after different time ofSO2＋CO reaction show that CeO2 is the active component that offers the redox couple Ce4＋/Ce3＋ and the labile oxygen vacancies, andTiO2 only functions as a catalyst structure stabilizer during the catalytic reaction process. After 48 h of catalytic reaction at 500℃,Ce0.7Ti0.3O2 still maintains a stable structure without being vulcanized, demonstrating its good anti-sulfur poisoning performance.展开更多
A series of Fe‐Mn/Al2O3 catalysts were prepared and studied for low temperature selective catalytic reduction （SCR） of NO with NH3 in a fixed‐bed reactor. The effects of Fe and Mn on NO conversion and the deactiva...A series of Fe‐Mn/Al2O3 catalysts were prepared and studied for low temperature selective catalytic reduction （SCR） of NO with NH3 in a fixed‐bed reactor. The effects of Fe and Mn on NO conversion and the deactivation of the catalysts were studied. N2 adsorption‐desorption, X‐ray diffraction, transmission electron microscopy, energy dispersive spectroscopy, H2 temperature‐programmed reduction, NH3 temperature‐programmed desorption, X‐ray photoelectron spectroscopy （XPS）, thermal gravimetric analysis and Fourier transform infrared spectroscopy were used to character‐ize the catalysts. The 8Fe‐8Mn/Al2O3 catalyst gave 99%of NO conversion at 150？？ and more than 92.6%NO conversion was obtained in a wide low temperature range of 90–210？？. XPS analysis demonstrated that the Fe3＋was the main iron valence state on the catalyst surface and the addition of Mn increased the accumulation of Fe on the surface. The higher specific surface area, enhanced dispersion of amorphous Fe and Mn, improved reduction properties and surface acidity, lower binding energy, higher Mn4＋/Mn3＋ratio and more adsorbed oxygen species resulted in higher NO conversion for the 8Fe‐8Mn/Al2O3 catalyst. In addition, the SCR activity of the 8Fe‐8Mn/Al2O3 cata‐lyst was only slightly decreased in the presence of H2O and SO2, which indicated that the catalyst had better tolerance to H2O and SO2. The reaction temperature was crucial for the SO2 resistance of catalyst and the decrease of catalytic activity caused by SO2 was mainly due to the sulfate salts formed on the catalyst.展开更多
CO oxidation is probably the most studied reaction in heterogeneous catalysis.This reaction has become a hot topic with the discovery of nanogold catalysts,which are active at low temperatures（at or below room temper...CO oxidation is probably the most studied reaction in heterogeneous catalysis.This reaction has become a hot topic with the discovery of nanogold catalysts,which are active at low temperatures（at or below room temperature）.Au catalysts are the benchmark for judging the activities of other metals in CO oxidation.Pt-group metals（PGMs） that give comparable performances are of particular interest.In this mini-review,we summarize the advances in various PGM（Pt,Pd,Ir,Rh,Ru）catalysts that have high catalytic activities in low-temperature CO oxidation arising from reducible supports or the presence of OH species.The effects of the size of the metal species and the importance of the interface between the metal and the reducible support are covered and discussed in terms of their promotional role in CO oxidation at low temperatures.展开更多
基金the National Key R&D Program of China(Grant No.2022YFA1602500)the National Natural Science Foundation of China(Grant No.12027809)Strategic Priority Research Program of the Chinese Academy of Sciences(Grant No.XDB21030900)。
文摘All of the experimentally known electronic states of the Cr group metal monoxides(Cr O,Mo O,and WO)have been presented in the paper.The optical spectra of the Cr O molecule have been investigated in the gas phase through a combination of the laser-induced fluorescence(LIF)excitation and single-vibronic-level(SVL)emission spectroscopy in the supersonic expansion.The rotational constants of the vibronic electronic states,including X^(5)Π_(-1)(v=0–3),B^(5)Π_(-1)(v=0–10),and B~5Π_1(v=1,5),and the vibrational constants of the spin–orbit components X^(5)Π_(-1,0,1)have been obtained.The molecular constants of the Mo O and WO molecules have been summarized by reviewing the previous spectroscopic studies,and a comprehensive energy level diagram of the Cr group metal monoxides has been constructed.By comparing the electronic configurations,bond lengths,and vibrational frequencies of all the transition metal monoxides in the ground electronic state,the significance of the relativistic effect in the bonding of the 5d transition metal monoxides has been discussed.The related spectroscopic data of the Cr O molecule are available at https://doi.org/10.57760/sciencedb.j00113.00085.
文摘It is challenging to diagnose isolated hyperbilirubinemia with rare and complex etiologies under the constraints of traditional testing conditions.Herein,we present a rare case of coexisting Gilbert syndrome(GS)and erythropoietic protoporphyria(EPP),which has not been previously documented.CASE SUMMARY We present a rare case of coexisting GS and EPP in a 23-year-old Chinese male with a long history of jaundice and recently found splenomegaly.Serial nonspecific hemolysis screening tests yielded inconsistent results,and investigations for common hemolytic etiologies were negative.However,Levitt’s carbon monoxide breath test,which measures erythrocyte lifespan(the gold-standard marker of hemolysis),demonstrated significant hemolysis,revealing a markedly shortened erythrocyte lifespan of 11 days(normal average 120 days).Genetic testing subsequently confirmed EPP with a homozygous ferrochelatase gene mutation and GS with a heterozygous uridine diphosphate glucuronosyl trans-ferase 1A1 gene mutation.CONCLUSION The rapid,non-invasive Levitt’s carbon monoxide breath test resolved the diagnostic challenge posed by a rare and complex cause of hyperbilirubinemia.
文摘Chiral carbonyl compounds frequently occur in natural products and pharmaceuticals. Additionally, they serve as important intermediates in organic synthesis. Transition metal-catalyzed asymmetric carbonylative cross-coupling reactions are among the most straightforward and effective methods for synthesizing chiral carbonyl compounds, including esters, amides, and ketones. The advances in asymmetric carbonylative cross-coupling reactions using various O-, N-, C-, and S-containing nucleophiles or electrophiles over the past decade are summarized.
基金supported by the Natural Science Foundation of Hunan Province(2021JJ31089)the Scientific Research Project of Health Commission of Hunan Province(202203104548),China。
文摘Objective:The neurotoxicity of carbon monoxide(CO)to the central nervous system is a key pathogenesis of delayed encephalopathy after acute carbon monoxide poisoning(DEACMP).Our previous study found that retinoic acid(RA)can suppress the neurotoxic effects of CO.This study further explores,in vivo and in vitro,the molecular mechanisms by which RA alleviates CO-induced central nervous system damage.Methods:A cytotoxic model was established using the mouse hippocampal neuronal cell line HT22 and primary oligodendrocytes exposed to CO,and a DEACMP animal model was established in adult Kunming mice.Cell viability and apoptosis of hippocampal neurons and oligodendrocytes were assessed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide(MTT)assay and Annexin V/propidium iodide(PI)double staining.The transcriptional and protein expression of each gene was detected using real time fluorescence quantitative PCR(RT-qPCR)and Western blotting.Long noncoding RNA(lncRNA)SNHG15 and LINGO-1 were knocked down or overexpressed to observe changes in neurons and oligodendrocytes.In DEACMP mice,SNHG15 or LINGO-1 were knocked down to assess changes in central nervous tissue and downstream protein expression.Results:RA at 10 and 20μmol/L significantly reversed CO-induced apoptosis of hippocampal neurons and oligodendrocytes,downregulation of SNHG15 and LINGO-1,and upregulation of brain-derived neurotrophic factor(BDNF)and tyrosine kinase receptor B(TrkB)(all P<0.05).Overexpression of SNHG15 or LINGO-1 weakened the protective effect of RA against CO-induced cytotoxicity(all P<0.05).Knockdown of SNHG15 or LINGO-1 alleviated CO-induced apoptosis of hippocampal neurons and oligodendrocytes and upregulated BDNF and TrkB expression levels(all P<0.05).Experiments in DEACMP model mice showed that knockdown of SNHG15 or LINGO-1 mitigated central nervous system injury in DEACMP(all P<0.05).Conclusion:RA alleviates CO-induced apoptosis of hippocampal neurons and oligodendrocytes,thereby reducing central nervous system injury and exerting neuroprotective effects.LncRNA SNHG15 and LINGO-1 are key molecules mediating RA induced inhibition of neuronal apoptosis and are associated with the BDNF/TrkB pathway.These findings provide a theoretical framework for optimizing the clinical treatment of DEACMP and lay an experimental foundation for elucidating its molecular mechanisms.
文摘This study systematically investigated the effects of experimental conditions,crystal phase,and microstructure on the preparation of V_(2)O_(3)for vanadium flow batteries by reducing ammonium metavanadate extracted from waste catalyst.The optimized experimental conditions were determined as follows:the CO reduction temperature was set at 575℃,the reduction time was 1 hour,the CO flow rate was 50 mL/min,and furnace cooling was performed subsequently.Under these conditions,the samples obtained were predominantly composed of single-phase V_(2)O_(3).Microstructural analysis reveals tightly packed grain configurations exhibiting flake-like or block-like morphologies.Significantly,the as-synthesized V_(2)O_(3)demonstrates sufficient purity for fabricating high-performance electrolytes in all-vanadium flow batteries,showing promising electrochemical applicability.
基金the National Natural Science Foundation of China(Nos.82272067,81974386,22107123 and M-0696)the Natural Science Foundation of Hunan Province(Nos.2021JJ41008,2022JJ80052,2022JJ40656,2023JJ20077)+2 种基金the Key Project of Changsha Science and Technology Plan(No.kh2201059)the Scientific Research Project of Health Commission of Hunan Province(No.B202313057213)the Youth Science Foundation of Xiangya Hospital(No.2022Q16).
文摘Carbon monoxide(CO)is a crucial gaseous signaling molecule that regulates various physiological and pathological processes,and may exert an anti-inflammatory and protective role in drug-induced liver injury(DILI).Despite this,understanding the exact relationship between CO and the occurrence and development of DILI remains challenging.Hence,there is an urgent need to develop a reliable and robust tool for the rapid visual detection and assessment of CO in this context.Herein,we presented a novel near-infrared(NIR)fluorescent nanoprobe with aggregation-induced emission(AIE)properties and excited-state intramolecular proton transfer(ESIPT)characteristics for the detection and imaging of CO both in vitro and in vivo.Simultaneously,the nanoprobe enables self-assembly form nanoaggregates in aqueous media with high biocompatible,which can sense CO in situ through the conversion of yellowto-red fluorescence facilitated aggregation-induced dual-color fluorescence.What is more,this nanoprobe shows ratiometric respond to CO,which demonstrates excellent stability,high sensitivity(with a detection limit of 12.5 nmol/L),and superior selectivity.Crucially,this nanoprobe enables the visual detection of exogenous and endogenous CO in living cells and tissues affected by DILI,offering a user-friendly tool for real-time visualization of CO in living system.Hence,it holds great promise in advancing our understanding of CO’s role.
基金supported by the Natural Science Foundation of Shandong Province(ZR2021MB135)the Major Scientific and Technological Innovation Project of Shandong Province(2021ZDSYS13).
文摘Cu(I)based CO adsorbents are prone to oxidation and deactivation owing to the sensitivity of Cu^(+) ions to oxygen and moisture in the humid air.In this study,in order to improve its antioxidant performance,hydrophobic Cu(I)based adsorbents were fabricated using polytetrafluoroethylene(PTFE)for the hydrophobic modification,effectively avoiding the contact of CuCl active species with moisture,thereby inhibiting the oxidation of the Cu(I)based adsorbents.The successful introduction of PTFE into the activated carbon(AC)carrier significantly improves the hydrophobicity of the adsorbent.The optimal adsorbent CuCl(6)@AC-PTFE(0.10%)with the CuCl loading of 6 mmol·g^(-1)and the PTFE mass concentration of 0.10%exhibits an excellent CO adsorption capacity of 3.61 mmol·g^(-1)(303 K,500 kPa)as well as high CO/CO_(2)and CO/N_(2)adsorption selectivities of 29 and 203(303 K,100 kPa).Particularly,compared with the unmodified adsorbents,the antioxidant performance of modified adsorbent CuCl(6)@AC-PTFE(0.10%)is significantly improved,holding 86%of CO adsorption performance of fresh one after 24 h of exposure to humid air with a relative humidity of 70%,making the fabricated composite a promising adsorbent for CO separation.
基金the financial support from the European Commission through the H2020-MSCA-RISE-2020 BIOALL project(Grant Agreement: 101008058)。
文摘Single carbon products(C1 compounds) are simple but important chemicals in the road towards energy transition.Catalytic conversion of CO_(2) with H_(2)(desirably renewable) can be performed over reducible oxides supporting transition metals to obtain products such as CH_(4),CO and MeOH.Oxygen vacancies(O-vacancies),which are inherent defects of reducible metal oxides,play an enormous role in driving the catalytic performance(activity,selectivity,stability) for the desired reactions.Yet,the assessment of O-defects at realistic conditions is often complex.Only few techniques can provide direct evidence for their existence and influence in CO_(2) activation.Among them,electron paramagnetic spectroscopy(EPR),Raman spectroscopy,scanning probe microscopies(SPM) and environmental transmission electron microscopy(ETEM) are nowadays the most informative.In most cases,however,the measurements require reaction conditions far away from CO_(2) valorization applications.Although great efforts have been fruitful in explaining and demonstrating the huge importance of O-vacancies in CO_(2) catalysis,still ambiguous or erroneous interpretations about structure-function correlations involving O-vacancies are found in literature,especially,when information is not properly gathered,e.g.,by O 1s ex-situ X-ray photon spectroscopy(XPS).Moreover,despite the recognized importance of O-vacancies for CO_(2) valorization,critical literature compilations about their effects in thermal processes are scarce.Herein,we attempt to contribute in closing this gap by integrally encompassing representative investigations on the thermo-catalytic production of CH_(4),CO and MeOH.Particularly,we emphasize on the proper selection of assessment tools(direct/indirect) to unambiguously establish structure-function relationships to design optimized O-defective catalysts for the targeted compounds.
基金financially supported by the National Natural Science Foundation of China(No.52301276)Zhejiang Provincial Natural Science Foundation of China(No.24E010001)+2 种基金Lishui Science and Technology Plan Project(No.2023GYX09)the support of the National Natural Science Foundation of China(52371229)Shanghai High-level Talent start funding
文摘The high hydrogen desorption density(19.6 wt%)of ammonia borane(AB)makes it one of the most promising chemical hydrogen storage materials.Developing cost-effective catalysts is the key for accelerating the hydrolysis of AB.Herein,we present a straightforward synthesis method for the Cu_(2)O decorated CoO catalyst derived from ZIF-67 precursors using carbothermal shock(~1 s)in air.The obtained results demonstrate that a small amount of Cu_(2)O doping into CoO synergistically enhances AB hydrolysis,resulting in an almost fivefold increase in turnover frequency(TOF=97 molH_(2)molCoO-1min-1at 298 K).Further studies indicated that the incorporation of Cu_(2)O alters the electronic distribution of the surface of catalysts,introducing more oxygen vacancies and increasing the pyridinic nitrogen content.The increased oxygen vacancies effectively enhanced the adsorption and activation ability of active sites for reactants(H_(2)O and AB),while the targeting effect of pyridinic nitrogen enhances the dispersion of the catalyst.Theoretical analysis reveals that CoO plays a key role in the dissociation of H_(2)O,while minor doping with Cu_(2)O substantially reduces the dissociation energy barrier of AB.This research provides a novel strategy for the design and efficient preparation of AB hydrolysis catalysts for efficient hydrogen production.
文摘The electrochemical carbon dioxide reduction reaction(CO_(2)RR)can convert carbon dioxide into highvalue chemical substances and fuels by utilizing renewable electricity,which can not only complete the carbon cycle but also effectively alleviate the problems of global warming and energy shortage.Nickelbased catalysts hold great promise and unbeatable merits for the electroreduction of carbon dioxide due to their excellent catalytic properties and activity.However,there were few review papers on the application of nickel-based catalysts in carbon dioxide electroreduction.This paper,therefore,presents the current status of research on nickel-based catalysts in carbon dioxide electroreduction categorized by different products.First,the advantages of CO_(2) electroreduction and nickel-based catalysts as well as the basic principles of CO_(2) electroreduction are presented;then the different types of nickel-based catalysts that can convert CO_(2) into different products are described in detail,including their syntheses,performances,and mechanisms.Finally,the common features of nickel-based catalysts towards different carbon dioxide electroreduction products,as well as the outlooks for the development of nickel-based catalysts will be summarized.It is highly expected that this review will help in the future research and development of nickel-based catalysts towards CO_(2) conversion.
基金financially supported by the National Natural Science Foundation of China(Nos.52379048 and 52079112)the Key Research and Development Program of Shaanxi Province,China(No.2022ZDLNY03-03)the Major Science and Technology Engineering Innovation Project of Shandong Province,China(No.2020CXGC 010808)。
文摘Aerated drip irrigation(ADI)is an important practice for promoting soil fertility and crop productivity in greenhouse vegetable production,yet little research has comprehensively investigated its effects on the functional traits of carbon(C)-cycling microorganisms.In this study,we sought to assess the potential efficacy of ADI in increasing soil organic C(SOC)by changing soil microbial communities and the expressions of genes associated with C cycling.To this end,we adopted a metagenomic approach to compare the effects of ADI with three dissolved oxygen concentrations(10,15,and 20 mg L^(-1))during a three-season tomato cultivation experiment in northern China.The results revealed that the 10 mg L^(-1)treatment led to a significant increase in the abundance of korA/B genes(associated with the reductive tricarboxylic acid cycle)in the C fixation pathway,whereas the 15 mg L^(-1)treatment increased the abundances of cbbL/R and coxL/S genes associated with the Calvin cycle and carbon monoxide oxidation,respectively.In addition,based on a co-occurrence network analysis,we observed a positive correlation between cbbL and coxS.Interestingly,r-selected microorganisms,such as Proteobacteria and Actinobacteria,characterized by rapid cell multiplication and high biomass production,were identified as the primary contributors to C fixation and were the main predictors of SOC pools.In contrast,the 20 mg L^(-1)treatment was found to adversely influence C fixation,although the enhanced C degradation could be attributed to the extracellular enzymes secreted by K-selected microorganisms.Collectively,our findings indicate that ADI with dissolved oxygen concentrations 15 mg L^(-1)can promote SOC content by altering the life history strategies of r-selected microorganisms and genes associated with C fixation.These findings will provide valuable references for agroecosystem irrigation management,help improve soil fertility,and promote sustainable production.
基金financial support from the National Natural Science Foundation of China(Nos.52204335 and 52374319)the National Nature Science Foundation of China(No.52174291)the Central Universities Foundation of China(No.06500170)。
文摘The experiment explored the Fe_(2)O_(3) reduction process with H_(2)/CO mixed gas and confirmed a promoting effect from CO when its volume proportion in mixed gas is 20% at 850℃.The ReaxFF molecular dynamics(MD)simulation method was used to observe the reduction process and provide an atomic-level explanation.The accuracy of the parameters used in the simulation was verified by the density functional theory(DFT)calculation.The simulation shows that the initial reduction rate of H_(2) is much faster than that of CO(from 800 to 950℃).As the reduction proceeds,cementite,obtained after CO participates in the reduction at 850℃,will appear on the iron surface.Due to the active properties of C atoms in cementite,they are easy to further react with the O atoms in Fe_(2)O_(3).The generation of internal CO may destroy the dense structure of the surface layer,thereby affecting the overall reduction swelling of Fe_(2)O_(3).However,excess CO is detrimental to the reaction rate,mainly because of the poor thermodynamic conditions of CO in the temperature range and the molecular diffusion capacity is not as good as that of H_(2).Furthermore,the surface structures obtained after H_(2) and CO reduction have been compared,and it was found that the structure obtained by CO reduction has a larger surface area,thus promoting the sub sequent reaction of H_(2).
基金supported by the FengYun Application Pioneering Project (Grant No. FY-APP-2022.0502)the National Natural Science Foundation of China (42205140)the State Key Laboratory of Atmospheric Environment end Extreme Meteorology (Grant No. 2024QN04)
文摘The Hyperspectral Infrared Atmospheric Sounder-II(HIRAS-II)onboard China’s FungYun(FY)-3F meteorological satellite was launched in August 2023.This study presents the first attempt to retrieve the global carbon monoxide(CO)column from HIRAS-II/FY-3F spectra based on a newly established full-physics algorithm.The CO global columns derived from the HIRAS-II/FY-3F satellite are compared to measurements from the Infrared Atmospheric Sounding Interferometer(IASI)onboard Europe’s MetopB satellite,as both satellites have the same spectral range with a similar overpass time.The correlation coefficient between the IASI/Metop-B and HIRAS-II/FY-3F CO retrievals is about 0.8.The HIRAS-II/FY-3F satellite can capture well the regions with high CO values,e.g.,Africa,North America,and East Asia.The relative difference in the CO global column between HIRAS-II and IASI is 1.2±13.7(1)%,which is within their combined retrieval uncertainty.The CO plumes from the fire emissions in North America between 18 and 23 July 2024 were observed by the HIRAS-II/FY-3F satellite and consistent with the CAMS(Copernicus Atmosphere Monitoring Service)model simulations.Our results show that the HIRAS-II/FY-3F spectra are of good enough quality to provide quantitative observations of global CO column remote sensing observations.
文摘Jet ventilation is widely used in the ventilation design of highway and railway tunnels as an important air supply method during tunnel operation and disaster periods.This ventilation method has also been applied for fire control in immersed tunnels.We conduct numerical simulations using computational fluid dynamics(CFD)to study positive ventilation in the upstream and reverse ventilation in the downstream(P-R)for an extra-wide immersed tunnel.The effects of fire source location and jet fan air velocity response strategy on the ceiling temperature decay,carbon monoxide(CO)distribution,and smoke exhaust efficiency were investigated for varying fire source locations.The results show that flames will be tilted to the side of the jet fan with a smaller air velocity.Additionally,the jet fan air velocity should be adjusted based on the relative distance between the fire source and the smoke vent.Among the studied scenarios,the most effective outcome was achieved when the air velocity was adjusted to 25 m/s on the side near the smoke vent.Also in this scenario,the phenomenon of smoke deposition was effectively mitigated and the average smoke exhaust efficiency reached 87%.Moreover,we found that the temperature decay of the tunnel follows an exponential decay law.The temperature decay rate is significantly higher on the side closest to the smoke vent compared to the farther side.This research provides a theoretical basis for smoke control strategies for fires that occur in immersed tunnels.
基金supported in part by National Key R&D Program of China(Grant No.2022YFE0141500)National Natural Science Foundation of China(Grant Nos.62004065 and 62274059).
文摘In this work,the incorporation of tantalum(Ta)into p-type metal-oxide(SnO_(x))semiconductor film is investigated to improve the electrical characteristics and suppress the fringe effect of thin film transistors(TFTs).The Ta-doped SnO_(x)(SnO_(x):Ta)film is deposited by radio-frequency(RF)magnetron sputtering with a Sn:Ta(3 at.%)target and thermally annealed at 270℃ for 30 min.Here,we observe that the SnO_(x):Ta film presents increased crystallinity,reduced defect density(3.25×10^(12)cm^(−2)·eV^(−1)),and widened bandgap(1.98 eV),in comparison with the undoped SnO_(x)film.As a result,the SnO_(x):Ta TFTs exhibit a lower off-state current(Ioff),an improved on/off current ratio(2.17×10^(4)),a remarkably decreased subthreshold swing(SS)by 41%,and enhanced device stability.Additionally,by introducing Ta dopants,the fringe effect as well as the impact of channel width-to-length ratio(W/L)on electrical performances of the p-type oxide TFTs can be effectively suppressed.These results shall contribute to further exploration and development of p-type SnO_(x)TFTs.
基金supported by the National Natural Science Foundation of China(Nos.22025604 and 22276204)the National Key R&D Program of China(Nos.2023YFC3708401 and 2022YFC3800404).
文摘To develop efficient catalysts for ambient carbon monoxide(CO)oxidation is significant for indoor air purification and also for many industrial applications.In this work,the catalytic activity for CO oxidation were enhanced by tuning the metal-support interaction of Ru/CeO_(2)catalysts.A series of Ru/CeO_(2)catalysts were synthesized by an impregnation method with calcination at 100,200,400 and 600℃,respectively,to regulate the Ru-CeO_(2)interaction.We discovered that low temperature calcination(100℃)induced more Ru-O-Ce bonds and stronger Ru-CeO_(2)interaction,while high temperature calcination(≥400℃)caused the agglomeration of Ru species with more Ru-O-Ru bonds and weaker Ru-CeO_(2)interaction,resulting in the lower redox capacity of these catalysts,as well as lower catalytic activity for CO oxidation.Only calcination at moderate 200℃ can induce the moderate interaction between Ru species and CeO_(2)support,which can keep the high dispersion of RuO_(x)species with the high redox capacity,thus leading to complete elimination of 500 ppm CO at room temperature on Ru/Ce-200 catalyst.
文摘The structure and catalytic desulfurization characteristics of CeO2-TiO2 mixed oxides were investigated by means ofX-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and catalytic activity tests. According to the results, a CeO2-TiO2solid solution is formed when the mole ratio of cerium to titanium n（Ce）：n（Ti） is 5：5 or greater, and the most suitable n（Ce）：n（Ti） isdetermined as 7：3, over which the conversion rate of SO2 and the yield of sulfur at 500℃ reach 93% and 99%, respectively.According to the activity testing curve, Ce0.7Ti0.3O2 （n（Ce）：n（Ti）=7：3） without any pretreatment can be gradually activated by reagentgas after about 10 min, and reaches a steady activation status 60 min later. The XPS results of Ce0.7Ti0.3O2 after different time ofSO2＋CO reaction show that CeO2 is the active component that offers the redox couple Ce4＋/Ce3＋ and the labile oxygen vacancies, andTiO2 only functions as a catalyst structure stabilizer during the catalytic reaction process. After 48 h of catalytic reaction at 500℃,Ce0.7Ti0.3O2 still maintains a stable structure without being vulcanized, demonstrating its good anti-sulfur poisoning performance.
基金supported by the National High Technology Research and Development Program of China (863 Program,2015AA03A401)the National Natural Science Foundation of China (51276039)+1 种基金the Fundamental Research Funds for the Central Universities (020514380020,020514380030)the Postdoctoral Science Foundation of Jiangsu Province,China (1501033A)~~
文摘A series of Fe‐Mn/Al2O3 catalysts were prepared and studied for low temperature selective catalytic reduction （SCR） of NO with NH3 in a fixed‐bed reactor. The effects of Fe and Mn on NO conversion and the deactivation of the catalysts were studied. N2 adsorption‐desorption, X‐ray diffraction, transmission electron microscopy, energy dispersive spectroscopy, H2 temperature‐programmed reduction, NH3 temperature‐programmed desorption, X‐ray photoelectron spectroscopy （XPS）, thermal gravimetric analysis and Fourier transform infrared spectroscopy were used to character‐ize the catalysts. The 8Fe‐8Mn/Al2O3 catalyst gave 99%of NO conversion at 150？？ and more than 92.6%NO conversion was obtained in a wide low temperature range of 90–210？？. XPS analysis demonstrated that the Fe3＋was the main iron valence state on the catalyst surface and the addition of Mn increased the accumulation of Fe on the surface. The higher specific surface area, enhanced dispersion of amorphous Fe and Mn, improved reduction properties and surface acidity, lower binding energy, higher Mn4＋/Mn3＋ratio and more adsorbed oxygen species resulted in higher NO conversion for the 8Fe‐8Mn/Al2O3 catalyst. In addition, the SCR activity of the 8Fe‐8Mn/Al2O3 cata‐lyst was only slightly decreased in the presence of H2O and SO2, which indicated that the catalyst had better tolerance to H2O and SO2. The reaction temperature was crucial for the SO2 resistance of catalyst and the decrease of catalytic activity caused by SO2 was mainly due to the sulfate salts formed on the catalyst.
基金supported by the National Natural Science Foundation of China(21076211,21203181,21576251,21676269)the "Strategic Priority Research Program" of the Chinese Academy of Sciences(XDB17020100)+1 种基金the National Key projects for Fundamental Research and Development of China(2016YFA0202801)Department of Science and Technology of Liaoning Province under contract of 2015020086-101~~
文摘CO oxidation is probably the most studied reaction in heterogeneous catalysis.This reaction has become a hot topic with the discovery of nanogold catalysts,which are active at low temperatures（at or below room temperature）.Au catalysts are the benchmark for judging the activities of other metals in CO oxidation.Pt-group metals（PGMs） that give comparable performances are of particular interest.In this mini-review,we summarize the advances in various PGM（Pt,Pd,Ir,Rh,Ru）catalysts that have high catalytic activities in low-temperature CO oxidation arising from reducible supports or the presence of OH species.The effects of the size of the metal species and the importance of the interface between the metal and the reducible support are covered and discussed in terms of their promotional role in CO oxidation at low temperatures.
