To accelerate the kinetics of the oxygen reduction reaction(ORR)in proton exchange membrane fuel cells,ultrafine Pt nanoparticles modified with trace amounts of cobalt were fabricated and decorated on carbon black thr...To accelerate the kinetics of the oxygen reduction reaction(ORR)in proton exchange membrane fuel cells,ultrafine Pt nanoparticles modified with trace amounts of cobalt were fabricated and decorated on carbon black through a strategy involving modified glycol reduction and chemical etching.The obtained Pt36Co/C catalyst exhibits a much larger electrochemical surface area(ECSA)and an improved ORR electrocatalytic activity compared to commercial Pt/C.Moreover,an electrode prepared with Pt36Co/C was further evaluated under H2-air single cell test conditions,and exhibited a maximum specific power density of 10.27 W mgPt^-1,which is 1.61 times higher than that of a conventional Pt/C electrode and also competitive with most state-of-the-art Pt-based architectures.In addition,the changes in ECSA,power density,and reacting resistance during the accelerated degradation process further demonstrate the enhanced durability of the Pt36Co/C electrode.The superior performance observed in this work can be attributed to the synergy between the ultrasmall size and homogeneous distribution of catalyst nanoparticles,bimetallic ligand and electronic effects,and the dissolution of unstable Co with the rearrangement of surface structure brought about by acid etching.Furthermore,the accessible raw materials and simplified operating procedures involved in the fabrication process would result in great cost-effectiveness for practical applications of PEMFCs.展开更多
Terbium can form a ternary complex having a ratio of 1:1:1 with acetylacetone and EDTA. By adding cetyl pyridinium chloride into the above system, a marked enhancement of fluorescence intensity is observed and the ter...Terbium can form a ternary complex having a ratio of 1:1:1 with acetylacetone and EDTA. By adding cetyl pyridinium chloride into the above system, a marked enhancement of fluorescence intensity is observed and the ternary complex becomes more stable than before. For analytical application, the derivative spectrofluorimetric method has high sensitivity and the effect of foreign ions is very low. The optimum conditions were obtained. The calibration graph is linear over 5～100μg/mL.展开更多
The derivative fluorimetric characteristics of Tb—SDS and Tb—SDS—phenanthroline systems have been studied. The optimum conditions were obtained. The 2nd—derivative spectrofluorimetric method in the systems has bee...The derivative fluorimetric characteristics of Tb—SDS and Tb—SDS—phenanthroline systems have been studied. The optimum conditions were obtained. The 2nd—derivative spectrofluorimetric method in the systems has been applied to the determination of trace amounts of terbium, in rare earth ore and their oxides. The results are satisfactory.展开更多
While foraging,animals can form inter-and intra-specific social signaling(i.e.one organism using signals to alert another about danger)networks to avoid similar predators.Honey bee sting alarm pheromones are multi-com...While foraging,animals can form inter-and intra-specific social signaling(i.e.one organism using signals to alert another about danger)networks to avoid similar predators.Honey bee sting alarm pheromones are multi-component blends,for instance isopentyl acetate(IPA),octyl acetate(OA),benzyl acetate(BA),etc.However,the展开更多
A An analytical method using high resolution inductively coupled plasma mass spectrometry （HR-ICP-MS） for rapid simultaneous determination of 24 elements （Be, Mg, A1, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Ge, As, Se, ...A An analytical method using high resolution inductively coupled plasma mass spectrometry （HR-ICP-MS） for rapid simultaneous determination of 24 elements （Be, Mg, A1, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Ge, As, Se, Mo, Ag, Cd, Sn Sb, Ba, Pt, Au, and Pb） in high purity cobalt was described. Sample digestions were performed in closed microwave vessels using HNO3 and HCI. The matrix effects because of the presence of excess HCI and Co were evaluated. The usefulness of high mass resolution for overcoming some spectral interference was demonstrated. The optimum conditions for the determination were tested and discussed. The standard addition method was employed for quantitative analysis. The detection limits were 0.016-1.50 ].tg·g^-1, the recovery ratios were 92.2%-111.2%, and the RSD was less than 3.6%. The method was accurate, quick, and convenient. It was applied to the determination of trace impurities in high purity cobalt with satisfactory results.展开更多
Reagents are optimized for the simultaneous determination of trace amounts of Cu^(2+), Cd^(2+) and Co^(2+) in zinc sulfate solution, which contains an extremely large excess of Zn^(2+). First, the reagents and their d...Reagents are optimized for the simultaneous determination of trace amounts of Cu^(2+), Cd^(2+) and Co^(2+) in zinc sulfate solution, which contains an extremely large excess of Zn^(2+). First, the reagents and their doses for the experiment are selected according to the characteristics of the zinc sulfate solution. Then, the reagent doses are optimized by analyzing the influence of reagent dose on the polarographic parameters(i.e. half-wave potential E_(1/2) and limiting diffusion current I_p). Finally, the optimization results are verified by simultaneously determining trace amounts of Cu^(2+), Cd^(2+) and Co^(2+) in the presence of an extremely large excess of Zn^(2+). The determination results indicate that the optimized reagents exhibit wide linearity, low detection limits, high accuracy and good precision for the simultaneous determination of trace amounts of Cu^(2+), Cd^(2+) and Co^(2+) in the presence of an extremely large excess of Zn^(2+).展开更多
An analytical method using high resolution inductively coupled plasma mass spectrometry （HR-ICP-MS） for rapid simultaneous determination of Be, Mg, Al, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Ge, As, Se, Mo, Ag, Cd, Sn, ...An analytical method using high resolution inductively coupled plasma mass spectrometry （HR-ICP-MS） for rapid simultaneous determination of Be, Mg, Al, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Ge, As, Se, Mo, Ag, Cd, Sn, Sb, Ba, Pt, Au and Pb in high purity cobalt was described. Sample digestions were performed in closed microwave vessels using HNO3 and HCl. The matrix effects due to the presence of excess HCl and Co were evaluated. The usefulness of high mass resolution for overcoming some spectral interference was demonstrated. The optimum conditions for the determination was tested and discussed. Correction for matrix effects, Sc, Rh and Bi were used as internal standards. The detection limits is 0.003-0.57 μg/g, the recovery ratio is 92.2%-111.2%, and the RSD is less than 3.6%. The method is accurate, quick and convenient. It has been applied to the determination of trace impurities in high purity cobalt with satisfactory results.展开更多
Using fewer catalysts to promote the chemical conversion of more substrates is the dream synthesis pursued by synthetic chemists.Achieving highly selective reactions using trace amounts(<1 ppm)of catalysts is rare ...Using fewer catalysts to promote the chemical conversion of more substrates is the dream synthesis pursued by synthetic chemists.Achieving highly selective reactions using trace amounts(<1 ppm)of catalysts is rare and has undoubted practical value.Herein,we designed and synthesized a single-atom Pd-metalated porous organic ligand polymer,denoted as Pd1@POL,and used the polymer to realize the regioselective hydrosilylation of allenes(Pd loading was as low as 0.98 ppm).The synergistic effect of the dispersed catalytic active sites in the catalyst and supports with ligand regulation function can directionally realize the formation of specifically configured hydrosilylation products.The as-fabricated single-atom catalyst(SAC;i.e.,Pd1@POL-5)showed an amazing catalytic efficiency and selectivity for hydrosilylation of allene(turnover number was up to 772,358,which was 200 times higher than previously recorded,and regioselectivity>100:1).The catalyst could be recycled numerous times in a continuous flow system without reductions in activity and selectivity.This work demonstrated the application prospect of the SAC in the synthesis of complex organic compounds and trace amount catalysis,which can lay the foundation for its large-scale and industrialized application in drug synthesis and other fields.展开更多
Quantitative detection of trace small-sized nanoplastics(<100 nm)remains a significant challenge in surface-enhanced Raman scattering(SERS).To tackle this issue,we developed a hydrophobic CuO@Ag nanowire substrate ...Quantitative detection of trace small-sized nanoplastics(<100 nm)remains a significant challenge in surface-enhanced Raman scattering(SERS).To tackle this issue,we developed a hydrophobic CuO@Ag nanowire substrate and introduced a multiplex-feature analysis strategy based on the coffee ring effect.This substrate not only offers high Raman enhancement but also exhibits a high probability of detection(POD),enabling rapid and accurate identification of 50 nm polystyrene nanoplastics over a broad concentration range(1–10−10 wt%).Importantly,experimental results reveal a strong correlation between the coffee ring formation and the concentration of nanoplastic dispersion.By incorporating Raman signal intensity,coffee ring diameter,and POD as combined features,we established a machine learning-based mapping between nanoplastic concentration and coffee ring characteristics,allowing precise predictions of dispersion concentration.The mean squared error of these predictions is remarkably low,ranging from 0.21 to 0.54,representing a 19 fold improvement in accuracy compared to traditional linear regression-based methods.This strategy effectively integrates SERS with wettability modification techniques,ensuring high sensitivity and fingerprinting capabilities,while addressing the limitations of Raman signal intensity in accurately reflecting concentration changes at ultra-low levels,providing a new idea for precise SERS measurements of nanoplastics.展开更多
The technology for green and macro-conversion of solid waste biomass to prepare high-quality activated carbon demands urgent development.This study proposes a technique for synthesizing carbon adsorbents using trace K...The technology for green and macro-conversion of solid waste biomass to prepare high-quality activated carbon demands urgent development.This study proposes a technique for synthesizing carbon adsorbents using trace KOH-catalyzed CO_(2) activation.Comprehensive investigations were conducted on three aspects:physicochemical structure evolution of biochar,mechanistic understanding of trace KOH-facilitated CO_(2) activation processes,and application characteristics for CO_(2) adsorption.Results demonstrate that biochar activated by trace KOH(<10%)and CO_(2) achieves comparable specific surface area(1244.09 m^(2)/g)to that obtained with 100%KOH activation(1425.10 m^(2)/g).The pore structure characteristics(specific surface area and pore volume)are governed by CO and CH4 generated through K-salt catalyzed reactions between CO_(2) and biochar.The optimal CO_(2) adsorption capacities of KBC adsorbent reached 4.70 mmol/g(0℃)and 7.25 mmol/g(25℃),representing the maximum values among comparable carbon adsorbents.The 5%KBC-CO_(2) sample exhibited CO_(2) adsorption capacities of 3.19 and 5.01 mmol/g under respective conditions,attaining current average performance levels.Notably,CO_(2)/N_(2) selectivity(85∶15,volume ratio)reached 64.71 at 0.02 bar with robust cycling stability.Molecular dynamics simulations revealed that oxygen-containing functional groups accelerate CO_(2) adsorption kinetics and enhance micropore storage capacity.This technical route offers simplicity,environmental compatibility,and scalability,providing critical references for large-scale preparation of high-quality carbon materials.展开更多
Field-and petrographic investigations,together with microanalytical major-and traceelement studies,were carried out on clinopyroxene and amphibole from high-Mg diorite in the subduction-related Chelyabinsk granitic ma...Field-and petrographic investigations,together with microanalytical major-and traceelement studies,were carried out on clinopyroxene and amphibole from high-Mg diorite in the subduction-related Chelyabinsk granitic massif to understand its petrogenesis and source.The clinopyroxene composition(high Mg#,Cr-content,sum of REE and Ti/Eu ratio;depletion in HREE;negative Eu-anomaly)indicates that it formed from a reduced melt derived from a mantle source metasomatized by fluids/melts having crustal affinity.Melt compositions in equilibrium with clinopyroxene and amphibole were calculated using solid/liquid partition coefficients.The high Nb/Y and Zr/Y ratio values of a liquid simulated from clinopyroxene,which appears to have very similar characteristics to sanukitoid melts,indicate a low degree of melting of the mantle source.Melt simulated from amphibole is more evolved and more felsic(dacitic).It displays a geochemical“amphibole fractionation”signature,indicating the peritectic transformation of clinopyroxene to amphibole in the lower crust.Rock textures and major element mineral compositions suggest that further amphibole was precipitated directly from the melt in the middle crust.The results show that the Chelyabinsk highMg diorite was probably formed as a cumulate from sanukitoid-like melt during its ascent and cooling below dacitic liquidus inside the amphibole stability field.展开更多
This work focused on determining the physico-chemical characteristics (pH, carbon and nitrogen) and trace metal elements (TMEs) content (As, Sb, Cd, Hg, Ni, Pb, Cr, Zn) of soils in the Brazzaville city. Soil samples w...This work focused on determining the physico-chemical characteristics (pH, carbon and nitrogen) and trace metal elements (TMEs) content (As, Sb, Cd, Hg, Ni, Pb, Cr, Zn) of soils in the Brazzaville city. Soil samples were taken from a depth of 0 to 20 cm using a hand auger on both banks of five tributaries of the Congo River (Djoué, Mfilou, Mfoa, Tsiémé, Djiri) that flow through the city of Brazzaville. 90 sampling points were defined, with 3 points 250 m apart on the banks and located, for each river, at three sites: upstream, midstream and downstream. Finally, 15 composite samples representative of the study area were taken. The average pH values of the water varied between 6.5 and 7.5. These pH values show that the soils studied are neutral. Total carbon content varied between 0.7% (Djiri) and 1.6% (Djoué). Total nitrogen content ranged from 0.08% (Djiri) to 0.12% (Djoué). TMEs contents varied from 0.5 to 1.8 mg/kg for Sb, from 0.5 to 2.5 mg/kg for As, from 0.1 to 0.18 mg/kg for Cd, from 4.2 to 11.3 mg/kg for Cr, from 0.07 to 0.27 mg/kg for Hg, from 0.7 to 2.4 mg/kg for Ni, from 0 to 158 mg/kg for Pb and from 16 to 105 mg/kg for Zn. The lowest TMEs levels were observed in the soils of the Djiri river, while the highest levels were observed in the soils of the Djoué and Tsiémé rivers. The ANOVA and Bonferroni test did not show significant differences in the means of the parameters measured (p > 0.05). The TMEs levels were below the accepted standards (NF U44-041), with the exception of Pb, which had high levels downstream of the Djoué. According to the pollution index values calculated using soil TME content, the soils on the banks of the Djoué river are considered polluted, while those on the banks of the Tsiémé river are moderately polluted, those on the banks of the Mfoa and Mfilou rivers are slightly polluted, and the soils on the banks of Djiri river are unpolluted.展开更多
Introduction: During pregnancy, the increased demand for all the nutrients required for the development of the foetus means that the maternal stock of trace elements and minerals may become unbalanced if dietary intak...Introduction: During pregnancy, the increased demand for all the nutrients required for the development of the foetus means that the maternal stock of trace elements and minerals may become unbalanced if dietary intake fails to compensate. The aim of this research is to determine the status of trace elements (calcium, copper, magnesium, selenium and zinc) in pregnant women in the city of Kisangani. Methods: We carried out an analytical cross-sectional study of non-pregnant and pregnant women living in Kisangani, from 05 October 2023 to 05 January 2024. Concentrations of trace elements in sera were analysed using an inductively coupled plasma mass spectrophotometer (ICP-MS Agilent 7700X). Statistical analysis of the data was performed using R software version 4.3.0. Results: The mean age was 26.3 ± 6.7 years;the mean copper and magnesium levels in the serum of pregnant women were 12.58 ± 1.13 micromol/l and 1.03 ± 1.03 mmol/l respectively. The medians for calcium and zinc were 1.49 mmol/l and 8.42 micromol/l. The selenium mode was 0.41 micromol/l. Variations in trace element levels in sera of pregnant women were 0.94 - 2.22 mmol/l for calcium;0.31 - 0.78 micromol/l for selenium;and 7.29 - 12.72 micromol/l for zinc;11.04 - 14.99 micromol/l for copper, and 0.082 - 1.05 mmol/l for magnesium. Conclusion: Serum trace element concentrations in pregnant women were lower than those observed in non-pregnant women. Trace element reserves in pregnant women depended on their nutrient status prior to pregnancy, hence, there was an urgent need for trace element balance prior to pregnancy.展开更多
Quartz trace elements are extensively employed in studying magmatic evolution,fluid evolution,and metal enrichment.The Bianjiadayuan Ag-Pb-Zn-Sn deposit is a typical magmatichydrothermal system in northeastern China,h...Quartz trace elements are extensively employed in studying magmatic evolution,fluid evolution,and metal enrichment.The Bianjiadayuan Ag-Pb-Zn-Sn deposit is a typical magmatichydrothermal system in northeastern China,however,studies on its complex magmatic-hydrothermal evolution are limited.This study investigates the quartz from the Bianjiadayuan deposit to gain insight into the physicochemical evolution of mineralization using cathodoluminescence(CL)textures and laser ablation-inductively coupled plasma-mass spectrometry(LA-ICP-MS)of quartz.Five types quartz(Q1 to Q5)were identified.From Q1 in quartz porphyry to Q5 in Ag-Pb-Zn veins,the CL intensity and Ti content gradually decreases,and Ge,Ge/Ti,and Al/Ti ratios increase,indicating a temperature decline from magmatic to hydrothermal stages.The Sb content shows an opposite trend to Ti content,correlating positively with Ge content in quartz,suggesting that Sb content could also be temperature-dependent.These trace elements in quartz indicate cooling is critical for Ag mineralization.Furthermore,quartz phenocryst(Q1)from the quartz porphyry shows low Al/Ti(mostly<4)and Ge/Ti ratios(<0.04),suggesting a low degree of magmatic evolution.The Sb content in Q5 from Ag-Pb-Zn-quartz veins(>1 ppm,mostly tens of ppm)is notably higher compared to quartz in other lithologies including Sn-bearing quartz veins(<1 ppm),suggesting that Sb contents can serve as an effective indicator of Ag mineralization.展开更多
It is of great importance to obtain precise trace data,as traces are frequently the sole visible and measurable parameter in most outcrops.The manual recognition and detection of traces on high-resolution three-dimens...It is of great importance to obtain precise trace data,as traces are frequently the sole visible and measurable parameter in most outcrops.The manual recognition and detection of traces on high-resolution three-dimensional(3D)models are relatively straightforward but time-consuming.One potential solution to enhance this process is to use machine learning algorithms to detect the 3D traces.In this study,a unique pixel-wise texture mapper algorithm generates a dense point cloud representation of an outcrop with the precise resolution of the original textured 3D model.A virtual digital image rendering was then employed to capture virtual images of selected regions.This technique helps to overcome limitations caused by the surface morphology of the rock mass,such as restricted access,lighting conditions,and shading effects.After AI-powered trace detection on two-dimensional(2D)images,a 3D data structuring technique was applied to the selected trace pixels.In the 3D data structuring,the trace data were structured through 2D thinning,3D reprojection,clustering,segmentation,and segment linking.Finally,the linked segments were exported as 3D polylines,with each polyline in the output corresponding to a trace.The efficacy of the proposed method was assessed using a 3D model of a real-world case study,which was used to compare the results of artificial intelligence(AI)-aided and human intelligence trace detection.Rosette diagrams,which visualize the distribution of trace orientations,confirmed the high similarity between the automatically and manually generated trace maps.In conclusion,the proposed semi-automatic method was easy to use,fast,and accurate in detecting the dominant jointing system of the rock mass.展开更多
Polyethylene oxide(PEO)-based solid-state polymer electrolytes(SPE)face the challenges of insufficient ionic conductivity and uncontrollable Li dendrite growth.The filler strategy can reinforce anode interface stabili...Polyethylene oxide(PEO)-based solid-state polymer electrolytes(SPE)face the challenges of insufficient ionic conductivity and uncontrollable Li dendrite growth.The filler strategy can reinforce anode interface stability,but at the cost of a large filler content(usually more than 10 wt%).This would increase the granular sensation,gravitational separation risk,and electrolyte membrane roughness with the creation of inhomogeneous Li^(+)transport channels between filler and polymer.Herein,we propose a trace filling strategy to address the above problems by introducing an amphoteric molecule L-Cysteine(LCy)as an eco-friendly and low-cost electrolyte additive.Only trace amount of LCy is required and integrated into PEO to form a homogenous,granule-less SPE with enhanced ionic conductivity and dendrite suppression capability.The ionic conductivity increases to 0.54 mS cm^(-1)at 60℃ after introducing only 1 wt%LCy.The amphotericity of LCy with basic–NH_(2)and acidic–COOH groups can promote the dissociation of Li salt and release more free Li ions through Lewis acid-base synergy,as well as the formation of multiple hydrogen bonds between PEO and LCy.The trace LCy additive swiftly leads to the formation of more ionic conductive interphases at both the anode and cathode sides.The composite SPE enables the stable cycling of Li metal for over 1400 h at 0.2 mA cm^(-2)and sustains a maximum current density up to 1.4 mA cm^(-2)in Li Li symmetric cells.The corresponding all-solid-state Li||FeF_(3)full cells exhibit a high specific capacity up to 567 mA h g^(-1)at 0.2 C and stable cycling performance for at least 700 cycles at 0.5 C with a high capacity retention.The excellent interface compatibility also guarantees the achievement of highcapacity Li-Fe-F conversion reaction even under the thin electrolyte membrane thickness and largerscale pouch cell configuration.展开更多
We investigated the concentrations,vertical distribution,and enrichment status of ten trace metal elements(Cr,Hg,Cu,Pb,Zn,Cd,As,Co,V,and Ni)in sediments of core D04 from the muddy area outside the Oujiang River Estuar...We investigated the concentrations,vertical distribution,and enrichment status of ten trace metal elements(Cr,Hg,Cu,Pb,Zn,Cd,As,Co,V,and Ni)in sediments of core D04 from the muddy area outside the Oujiang River Estuary.In addition to V,As,and Hg,the concentrations of Cr,Cu,Zn,Pb,Cd,Ni and Co were constrained by sediment grain size and organic matter.Al-though the concentrations of trace metals fluctuated during the 5.8–2.5 kyr BP period,overall variations remained relatively stable.However,during the 2.5–0 kyr BP period,the concentrations of Cd,Zn,Cu,Pb,Ni,Ni,and Cr showed an increasing trend within the fluctuations,ultimately reaching relatively high levels.The muddy area was lightly contaminated by heavy metals such as As,Hg,and Cu.The concentrations of Hg,As,and Cu have been continuously increasing since 2.5 kyr BP,indicating clear impacts from fre-quent human activities.展开更多
This review systematically summarizes the core advances in the field of trace elements and tumors,and clarifies the dual roles of key elements such as Zn,Cu,Fe,Se,Mn,and Ni in tumorigenesis(e.g.,DNA damage repair),tum...This review systematically summarizes the core advances in the field of trace elements and tumors,and clarifies the dual roles of key elements such as Zn,Cu,Fe,Se,Mn,and Ni in tumorigenesis(e.g.,DNA damage repair),tumor progression(e.g.,tumor microenvironment regulation),and therapeutic response-these elements not only possess tumor-suppressive potential but can also contribute to tumorigenesis.Meanwhile,it confirms the breakthrough value of multi-omics technologies and organoid models in deciphering the“element-cell-tumor”interaction mechanisms,which overcomes the limitations of traditional in vitro experiments and also points out the core directions for subsequent clinical research.展开更多
文摘To accelerate the kinetics of the oxygen reduction reaction(ORR)in proton exchange membrane fuel cells,ultrafine Pt nanoparticles modified with trace amounts of cobalt were fabricated and decorated on carbon black through a strategy involving modified glycol reduction and chemical etching.The obtained Pt36Co/C catalyst exhibits a much larger electrochemical surface area(ECSA)and an improved ORR electrocatalytic activity compared to commercial Pt/C.Moreover,an electrode prepared with Pt36Co/C was further evaluated under H2-air single cell test conditions,and exhibited a maximum specific power density of 10.27 W mgPt^-1,which is 1.61 times higher than that of a conventional Pt/C electrode and also competitive with most state-of-the-art Pt-based architectures.In addition,the changes in ECSA,power density,and reacting resistance during the accelerated degradation process further demonstrate the enhanced durability of the Pt36Co/C electrode.The superior performance observed in this work can be attributed to the synergy between the ultrasmall size and homogeneous distribution of catalyst nanoparticles,bimetallic ligand and electronic effects,and the dissolution of unstable Co with the rearrangement of surface structure brought about by acid etching.Furthermore,the accessible raw materials and simplified operating procedures involved in the fabrication process would result in great cost-effectiveness for practical applications of PEMFCs.
基金Project supported by the National Natural Science Foundation of China
文摘Terbium can form a ternary complex having a ratio of 1:1:1 with acetylacetone and EDTA. By adding cetyl pyridinium chloride into the above system, a marked enhancement of fluorescence intensity is observed and the ternary complex becomes more stable than before. For analytical application, the derivative spectrofluorimetric method has high sensitivity and the effect of foreign ions is very low. The optimum conditions were obtained. The calibration graph is linear over 5～100μg/mL.
基金Project supported by the National Natural Science Foundation of China
文摘The derivative fluorimetric characteristics of Tb—SDS and Tb—SDS—phenanthroline systems have been studied. The optimum conditions were obtained. The 2nd—derivative spectrofluorimetric method in the systems has been applied to the determination of trace amounts of terbium, in rare earth ore and their oxides. The results are satisfactory.
文摘While foraging,animals can form inter-and intra-specific social signaling(i.e.one organism using signals to alert another about danger)networks to avoid similar predators.Honey bee sting alarm pheromones are multi-component blends,for instance isopentyl acetate(IPA),octyl acetate(OA),benzyl acetate(BA),etc.However,the
基金the Natural Science Foundation of Hunan Province, China (No. 05JJ40017).
文摘A An analytical method using high resolution inductively coupled plasma mass spectrometry （HR-ICP-MS） for rapid simultaneous determination of 24 elements （Be, Mg, A1, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Ge, As, Se, Mo, Ag, Cd, Sn Sb, Ba, Pt, Au, and Pb） in high purity cobalt was described. Sample digestions were performed in closed microwave vessels using HNO3 and HCI. The matrix effects because of the presence of excess HCI and Co were evaluated. The usefulness of high mass resolution for overcoming some spectral interference was demonstrated. The optimum conditions for the determination were tested and discussed. The standard addition method was employed for quantitative analysis. The detection limits were 0.016-1.50 ].tg·g^-1, the recovery ratios were 92.2%-111.2%, and the RSD was less than 3.6%. The method was accurate, quick, and convenient. It was applied to the determination of trace impurities in high purity cobalt with satisfactory results.
基金Projects(61533021,61321003,61273185)supported by the National Natural Science Foundation of ChinaProject(2015CX007)supported by the Innovation-driven Plan in Central South University,ChinaProject(13JJ8003)supported by the Joint Fund of Hunan Provincial Natural Science Foundation of China
文摘Reagents are optimized for the simultaneous determination of trace amounts of Cu^(2+), Cd^(2+) and Co^(2+) in zinc sulfate solution, which contains an extremely large excess of Zn^(2+). First, the reagents and their doses for the experiment are selected according to the characteristics of the zinc sulfate solution. Then, the reagent doses are optimized by analyzing the influence of reagent dose on the polarographic parameters(i.e. half-wave potential E_(1/2) and limiting diffusion current I_p). Finally, the optimization results are verified by simultaneously determining trace amounts of Cu^(2+), Cd^(2+) and Co^(2+) in the presence of an extremely large excess of Zn^(2+). The determination results indicate that the optimized reagents exhibit wide linearity, low detection limits, high accuracy and good precision for the simultaneous determination of trace amounts of Cu^(2+), Cd^(2+) and Co^(2+) in the presence of an extremely large excess of Zn^(2+).
基金supported by the Natural Science Foundation of Hunan Province(No.05JJ40017)Education Department of Hunan Province(No.05B064).
文摘An analytical method using high resolution inductively coupled plasma mass spectrometry （HR-ICP-MS） for rapid simultaneous determination of Be, Mg, Al, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Ge, As, Se, Mo, Ag, Cd, Sn, Sb, Ba, Pt, Au and Pb in high purity cobalt was described. Sample digestions were performed in closed microwave vessels using HNO3 and HCl. The matrix effects due to the presence of excess HCl and Co were evaluated. The usefulness of high mass resolution for overcoming some spectral interference was demonstrated. The optimum conditions for the determination was tested and discussed. Correction for matrix effects, Sc, Rh and Bi were used as internal standards. The detection limits is 0.003-0.57 μg/g, the recovery ratio is 92.2%-111.2%, and the RSD is less than 3.6%. The method is accurate, quick and convenient. It has been applied to the determination of trace impurities in high purity cobalt with satisfactory results.
基金the Guangxi Natural Science Foundation of China(No.2021GXNSFFA220005)the central government guides local science and technology development fund projects(No.guike ZY21195014)+1 种基金the National Natural Science Foundation of China(Nos.22061003 and 22161008)the Opening Project of Hunan Engineering Laboratory for Analyse and Drugs Development of Ethnomedicine in Wuling Mountain(No.hgxy2101)for financial support.
文摘Using fewer catalysts to promote the chemical conversion of more substrates is the dream synthesis pursued by synthetic chemists.Achieving highly selective reactions using trace amounts(<1 ppm)of catalysts is rare and has undoubted practical value.Herein,we designed and synthesized a single-atom Pd-metalated porous organic ligand polymer,denoted as Pd1@POL,and used the polymer to realize the regioselective hydrosilylation of allenes(Pd loading was as low as 0.98 ppm).The synergistic effect of the dispersed catalytic active sites in the catalyst and supports with ligand regulation function can directionally realize the formation of specifically configured hydrosilylation products.The as-fabricated single-atom catalyst(SAC;i.e.,Pd1@POL-5)showed an amazing catalytic efficiency and selectivity for hydrosilylation of allene(turnover number was up to 772,358,which was 200 times higher than previously recorded,and regioselectivity>100:1).The catalyst could be recycled numerous times in a continuous flow system without reductions in activity and selectivity.This work demonstrated the application prospect of the SAC in the synthesis of complex organic compounds and trace amount catalysis,which can lay the foundation for its large-scale and industrialized application in drug synthesis and other fields.
基金the National Natural Science Foundation of China(No.12174229 and 22375117)Natural Science Foundation of Shandong Province(No.ZR2022YQ02 and ZR2023MB149)Taishan Scholars Program of Shandong Province(No.tsqn202306152)for financial support.
文摘Quantitative detection of trace small-sized nanoplastics(<100 nm)remains a significant challenge in surface-enhanced Raman scattering(SERS).To tackle this issue,we developed a hydrophobic CuO@Ag nanowire substrate and introduced a multiplex-feature analysis strategy based on the coffee ring effect.This substrate not only offers high Raman enhancement but also exhibits a high probability of detection(POD),enabling rapid and accurate identification of 50 nm polystyrene nanoplastics over a broad concentration range(1–10−10 wt%).Importantly,experimental results reveal a strong correlation between the coffee ring formation and the concentration of nanoplastic dispersion.By incorporating Raman signal intensity,coffee ring diameter,and POD as combined features,we established a machine learning-based mapping between nanoplastic concentration and coffee ring characteristics,allowing precise predictions of dispersion concentration.The mean squared error of these predictions is remarkably low,ranging from 0.21 to 0.54,representing a 19 fold improvement in accuracy compared to traditional linear regression-based methods.This strategy effectively integrates SERS with wettability modification techniques,ensuring high sensitivity and fingerprinting capabilities,while addressing the limitations of Raman signal intensity in accurately reflecting concentration changes at ultra-low levels,providing a new idea for precise SERS measurements of nanoplastics.
基金supported by the National Natural Science Foundation of China(52376103,542B2081).
文摘The technology for green and macro-conversion of solid waste biomass to prepare high-quality activated carbon demands urgent development.This study proposes a technique for synthesizing carbon adsorbents using trace KOH-catalyzed CO_(2) activation.Comprehensive investigations were conducted on three aspects:physicochemical structure evolution of biochar,mechanistic understanding of trace KOH-facilitated CO_(2) activation processes,and application characteristics for CO_(2) adsorption.Results demonstrate that biochar activated by trace KOH(<10%)and CO_(2) achieves comparable specific surface area(1244.09 m^(2)/g)to that obtained with 100%KOH activation(1425.10 m^(2)/g).The pore structure characteristics(specific surface area and pore volume)are governed by CO and CH4 generated through K-salt catalyzed reactions between CO_(2) and biochar.The optimal CO_(2) adsorption capacities of KBC adsorbent reached 4.70 mmol/g(0℃)and 7.25 mmol/g(25℃),representing the maximum values among comparable carbon adsorbents.The 5%KBC-CO_(2) sample exhibited CO_(2) adsorption capacities of 3.19 and 5.01 mmol/g under respective conditions,attaining current average performance levels.Notably,CO_(2)/N_(2) selectivity(85∶15,volume ratio)reached 64.71 at 0.02 bar with robust cycling stability.Molecular dynamics simulations revealed that oxygen-containing functional groups accelerate CO_(2) adsorption kinetics and enhance micropore storage capacity.This technical route offers simplicity,environmental compatibility,and scalability,providing critical references for large-scale preparation of high-quality carbon materials.
文摘Field-and petrographic investigations,together with microanalytical major-and traceelement studies,were carried out on clinopyroxene and amphibole from high-Mg diorite in the subduction-related Chelyabinsk granitic massif to understand its petrogenesis and source.The clinopyroxene composition(high Mg#,Cr-content,sum of REE and Ti/Eu ratio;depletion in HREE;negative Eu-anomaly)indicates that it formed from a reduced melt derived from a mantle source metasomatized by fluids/melts having crustal affinity.Melt compositions in equilibrium with clinopyroxene and amphibole were calculated using solid/liquid partition coefficients.The high Nb/Y and Zr/Y ratio values of a liquid simulated from clinopyroxene,which appears to have very similar characteristics to sanukitoid melts,indicate a low degree of melting of the mantle source.Melt simulated from amphibole is more evolved and more felsic(dacitic).It displays a geochemical“amphibole fractionation”signature,indicating the peritectic transformation of clinopyroxene to amphibole in the lower crust.Rock textures and major element mineral compositions suggest that further amphibole was precipitated directly from the melt in the middle crust.The results show that the Chelyabinsk highMg diorite was probably formed as a cumulate from sanukitoid-like melt during its ascent and cooling below dacitic liquidus inside the amphibole stability field.
文摘This work focused on determining the physico-chemical characteristics (pH, carbon and nitrogen) and trace metal elements (TMEs) content (As, Sb, Cd, Hg, Ni, Pb, Cr, Zn) of soils in the Brazzaville city. Soil samples were taken from a depth of 0 to 20 cm using a hand auger on both banks of five tributaries of the Congo River (Djoué, Mfilou, Mfoa, Tsiémé, Djiri) that flow through the city of Brazzaville. 90 sampling points were defined, with 3 points 250 m apart on the banks and located, for each river, at three sites: upstream, midstream and downstream. Finally, 15 composite samples representative of the study area were taken. The average pH values of the water varied between 6.5 and 7.5. These pH values show that the soils studied are neutral. Total carbon content varied between 0.7% (Djiri) and 1.6% (Djoué). Total nitrogen content ranged from 0.08% (Djiri) to 0.12% (Djoué). TMEs contents varied from 0.5 to 1.8 mg/kg for Sb, from 0.5 to 2.5 mg/kg for As, from 0.1 to 0.18 mg/kg for Cd, from 4.2 to 11.3 mg/kg for Cr, from 0.07 to 0.27 mg/kg for Hg, from 0.7 to 2.4 mg/kg for Ni, from 0 to 158 mg/kg for Pb and from 16 to 105 mg/kg for Zn. The lowest TMEs levels were observed in the soils of the Djiri river, while the highest levels were observed in the soils of the Djoué and Tsiémé rivers. The ANOVA and Bonferroni test did not show significant differences in the means of the parameters measured (p > 0.05). The TMEs levels were below the accepted standards (NF U44-041), with the exception of Pb, which had high levels downstream of the Djoué. According to the pollution index values calculated using soil TME content, the soils on the banks of the Djoué river are considered polluted, while those on the banks of the Tsiémé river are moderately polluted, those on the banks of the Mfoa and Mfilou rivers are slightly polluted, and the soils on the banks of Djiri river are unpolluted.
文摘Introduction: During pregnancy, the increased demand for all the nutrients required for the development of the foetus means that the maternal stock of trace elements and minerals may become unbalanced if dietary intake fails to compensate. The aim of this research is to determine the status of trace elements (calcium, copper, magnesium, selenium and zinc) in pregnant women in the city of Kisangani. Methods: We carried out an analytical cross-sectional study of non-pregnant and pregnant women living in Kisangani, from 05 October 2023 to 05 January 2024. Concentrations of trace elements in sera were analysed using an inductively coupled plasma mass spectrophotometer (ICP-MS Agilent 7700X). Statistical analysis of the data was performed using R software version 4.3.0. Results: The mean age was 26.3 ± 6.7 years;the mean copper and magnesium levels in the serum of pregnant women were 12.58 ± 1.13 micromol/l and 1.03 ± 1.03 mmol/l respectively. The medians for calcium and zinc were 1.49 mmol/l and 8.42 micromol/l. The selenium mode was 0.41 micromol/l. Variations in trace element levels in sera of pregnant women were 0.94 - 2.22 mmol/l for calcium;0.31 - 0.78 micromol/l for selenium;and 7.29 - 12.72 micromol/l for zinc;11.04 - 14.99 micromol/l for copper, and 0.082 - 1.05 mmol/l for magnesium. Conclusion: Serum trace element concentrations in pregnant women were lower than those observed in non-pregnant women. Trace element reserves in pregnant women depended on their nutrient status prior to pregnancy, hence, there was an urgent need for trace element balance prior to pregnancy.
基金supported by the National Natural Science Foundation of China(No.42222205)the National Key Research and Development Program of China(No.2017YFC0602403)the Fundamental Research Funds for the Central Universities,CHD(No.300102273301)。
文摘Quartz trace elements are extensively employed in studying magmatic evolution,fluid evolution,and metal enrichment.The Bianjiadayuan Ag-Pb-Zn-Sn deposit is a typical magmatichydrothermal system in northeastern China,however,studies on its complex magmatic-hydrothermal evolution are limited.This study investigates the quartz from the Bianjiadayuan deposit to gain insight into the physicochemical evolution of mineralization using cathodoluminescence(CL)textures and laser ablation-inductively coupled plasma-mass spectrometry(LA-ICP-MS)of quartz.Five types quartz(Q1 to Q5)were identified.From Q1 in quartz porphyry to Q5 in Ag-Pb-Zn veins,the CL intensity and Ti content gradually decreases,and Ge,Ge/Ti,and Al/Ti ratios increase,indicating a temperature decline from magmatic to hydrothermal stages.The Sb content shows an opposite trend to Ti content,correlating positively with Ge content in quartz,suggesting that Sb content could also be temperature-dependent.These trace elements in quartz indicate cooling is critical for Ag mineralization.Furthermore,quartz phenocryst(Q1)from the quartz porphyry shows low Al/Ti(mostly<4)and Ge/Ti ratios(<0.04),suggesting a low degree of magmatic evolution.The Sb content in Q5 from Ag-Pb-Zn-quartz veins(>1 ppm,mostly tens of ppm)is notably higher compared to quartz in other lithologies including Sn-bearing quartz veins(<1 ppm),suggesting that Sb contents can serve as an effective indicator of Ag mineralization.
基金supported by grants from the Human Resources Development program (Grant No.20204010600250)the Training Program of CCUS for the Green Growth (Grant No.20214000000500)by the Korea Institute of Energy Technology Evaluation and Planning (KETEP)funded by the Ministry of Trade,Industry,and Energy of the Korean Government (MOTIE).
文摘It is of great importance to obtain precise trace data,as traces are frequently the sole visible and measurable parameter in most outcrops.The manual recognition and detection of traces on high-resolution three-dimensional(3D)models are relatively straightforward but time-consuming.One potential solution to enhance this process is to use machine learning algorithms to detect the 3D traces.In this study,a unique pixel-wise texture mapper algorithm generates a dense point cloud representation of an outcrop with the precise resolution of the original textured 3D model.A virtual digital image rendering was then employed to capture virtual images of selected regions.This technique helps to overcome limitations caused by the surface morphology of the rock mass,such as restricted access,lighting conditions,and shading effects.After AI-powered trace detection on two-dimensional(2D)images,a 3D data structuring technique was applied to the selected trace pixels.In the 3D data structuring,the trace data were structured through 2D thinning,3D reprojection,clustering,segmentation,and segment linking.Finally,the linked segments were exported as 3D polylines,with each polyline in the output corresponding to a trace.The efficacy of the proposed method was assessed using a 3D model of a real-world case study,which was used to compare the results of artificial intelligence(AI)-aided and human intelligence trace detection.Rosette diagrams,which visualize the distribution of trace orientations,confirmed the high similarity between the automatically and manually generated trace maps.In conclusion,the proposed semi-automatic method was easy to use,fast,and accurate in detecting the dominant jointing system of the rock mass.
基金supported by National Natural Science Foundation of China(52372249 and 52102329)the support from the Program of Shanghai Academic Research Leader(21XD1424400)。
文摘Polyethylene oxide(PEO)-based solid-state polymer electrolytes(SPE)face the challenges of insufficient ionic conductivity and uncontrollable Li dendrite growth.The filler strategy can reinforce anode interface stability,but at the cost of a large filler content(usually more than 10 wt%).This would increase the granular sensation,gravitational separation risk,and electrolyte membrane roughness with the creation of inhomogeneous Li^(+)transport channels between filler and polymer.Herein,we propose a trace filling strategy to address the above problems by introducing an amphoteric molecule L-Cysteine(LCy)as an eco-friendly and low-cost electrolyte additive.Only trace amount of LCy is required and integrated into PEO to form a homogenous,granule-less SPE with enhanced ionic conductivity and dendrite suppression capability.The ionic conductivity increases to 0.54 mS cm^(-1)at 60℃ after introducing only 1 wt%LCy.The amphotericity of LCy with basic–NH_(2)and acidic–COOH groups can promote the dissociation of Li salt and release more free Li ions through Lewis acid-base synergy,as well as the formation of multiple hydrogen bonds between PEO and LCy.The trace LCy additive swiftly leads to the formation of more ionic conductive interphases at both the anode and cathode sides.The composite SPE enables the stable cycling of Li metal for over 1400 h at 0.2 mA cm^(-2)and sustains a maximum current density up to 1.4 mA cm^(-2)in Li Li symmetric cells.The corresponding all-solid-state Li||FeF_(3)full cells exhibit a high specific capacity up to 567 mA h g^(-1)at 0.2 C and stable cycling performance for at least 700 cycles at 0.5 C with a high capacity retention.The excellent interface compatibility also guarantees the achievement of highcapacity Li-Fe-F conversion reaction even under the thin electrolyte membrane thickness and largerscale pouch cell configuration.
基金funded by National Natural Science Foundation of China(No.41706074)Natural Science Foundation of Shandong Province(No.ZR2022 MD114)Geological Environment Investigation and Monitoring of the Coastal Zone in the Yangtze River Estuary(No.DD20242714).
文摘We investigated the concentrations,vertical distribution,and enrichment status of ten trace metal elements(Cr,Hg,Cu,Pb,Zn,Cd,As,Co,V,and Ni)in sediments of core D04 from the muddy area outside the Oujiang River Estuary.In addition to V,As,and Hg,the concentrations of Cr,Cu,Zn,Pb,Cd,Ni and Co were constrained by sediment grain size and organic matter.Al-though the concentrations of trace metals fluctuated during the 5.8–2.5 kyr BP period,overall variations remained relatively stable.However,during the 2.5–0 kyr BP period,the concentrations of Cd,Zn,Cu,Pb,Ni,Ni,and Cr showed an increasing trend within the fluctuations,ultimately reaching relatively high levels.The muddy area was lightly contaminated by heavy metals such as As,Hg,and Cu.The concentrations of Hg,As,and Cu have been continuously increasing since 2.5 kyr BP,indicating clear impacts from fre-quent human activities.
文摘This review systematically summarizes the core advances in the field of trace elements and tumors,and clarifies the dual roles of key elements such as Zn,Cu,Fe,Se,Mn,and Ni in tumorigenesis(e.g.,DNA damage repair),tumor progression(e.g.,tumor microenvironment regulation),and therapeutic response-these elements not only possess tumor-suppressive potential but can also contribute to tumorigenesis.Meanwhile,it confirms the breakthrough value of multi-omics technologies and organoid models in deciphering the“element-cell-tumor”interaction mechanisms,which overcomes the limitations of traditional in vitro experiments and also points out the core directions for subsequent clinical research.
