Patients with advanced liver cirrhosis and liver failure frequently experience abnormalities in their serum electrolyte levels.In such patients,hyponatremia has been identified as a predictor of poor outcomes.However,...Patients with advanced liver cirrhosis and liver failure frequently experience abnormalities in their serum electrolyte levels.In such patients,hyponatremia has been identified as a predictor of poor outcomes.However,emerging evidence suggests that serum chloride may provide even better prognostic information in similar situations.Hypochloremia,characterised by low serum chloride levels,has been linked to increased mortality,exacerbated organ dysfunction,and higher requirements for renal replacement therapy and vasopressors in various critical conditions,including advanced liver diseases.The pathophysiological mecha-nisms underlying the association between low serum chloride levels and poor outcomes in liver disease appear to involve complex interactions among electro-lyte imbalances,renal function,and systemic hemodynamics.Chloride dysregu-lation can influence renal salt-sensing mechanisms,disrupt acid-base homeostasis,and exacerbate complications such as hepatic encephalopathy and hepatorenal syndrome.This article aims to elucidate the prognostic significance of lower serum chloride levels in patients with advanced liver disease.By reviewing recent literature and analysing clinical data,we seek to establish serum chloride as an underutilised but valuable prognostic marker.Understanding the role of serum chloride in liver disease could enhance prognostic accuracy,refine treatment strategies,and ultimately improve patient outcomes.展开更多
Recycling plastic waste into triboelectric nanogenerators(TENGs)presents a sustainable approach to energy harvesting,self-powered sensing,and environmental remediation.This study investigates the recycling of polyviny...Recycling plastic waste into triboelectric nanogenerators(TENGs)presents a sustainable approach to energy harvesting,self-powered sensing,and environmental remediation.This study investigates the recycling of polyvinyl chloride(PVC)pipe waste polymers into nanofibers(NFs)optimized for TENG applications.We focused on optimizing the morphology of recycled PVC polymer to NFs and enhancing their piezoelectric properties by incorporating ZnO nanoparticles(NPs).The optimized PVC/0.5 wt%ZnO NFs were tested with Nylon-6 NFs,and copper(Cu)electrodes.The Nylon-6 NFs exhibited a power density of 726.3μWcm^(-2)—1.13 times higher than Cu and maintained 90%stability after 172800 cycles,successfully powering various colored LEDs.Additionally,a 3D-designed device was developed to harvest energy from biomechanical movements such as finger tapping,hand tapping,and foot pressing,making it suitable for wearable energy harvesting,automatic switches,and invisible sensors in surveillance systems.This study demonstrates that recycling polymers for TENG devices can effectively address energy,sensor,and environmental challenges.展开更多
BACKGROUND Colorectal cancer(CRC)is the third most common cancer globally,causing over 900000 deaths annually.Risk factors include aging,diet,obesity,sedentary lifestyle,tobacco use,genetic predisposition,and inflamma...BACKGROUND Colorectal cancer(CRC)is the third most common cancer globally,causing over 900000 deaths annually.Risk factors include aging,diet,obesity,sedentary lifestyle,tobacco use,genetic predisposition,and inflammatory bowel disease.Despite current treatments,survival rates for advanced CRC remain low,highlighting the need for better therapeutic strategies.AIM To evaluate both the clinical significance and the pathological implications of the Kinesin family member 14(KIF14)expression within CRC specimens.Additionally,this study aims to investigate the interaction between nitidine chloride(NC)and KIF14,considering their potential as therapeutic targets.METHODS The expression of the KIF14 protein in CRC was analyzed using immunohistochemical staining.The integration of multicenter high-throughput data facilitated the calculation of the standardized mean difference(SMD)for KIF14 mRNA levels.The assessment of clinical and pathological impact was enhanced by analyzing combined receiver operating characteristic curves,along with measures of sensitivity,specificity,and likelihood ratios.Additionally,clustered regularly interspaced short palindromic repeats knockout screening for cell growth and single-cell sequencing were employed to validate the significance of KIF14 expression in CRC.Survival analysis established the prognostic value of KIF14 in CRC.The molecular mechanism of NC against CRC was elucidated through whole-genome sequencing and enrichment analysis,and molecular docking was utilized to explore the targeting affinity between NC and KIF14.RESULTS KIF14 was highly expressed in 208 CRC patients.Data from 17 platforms involving 2436 CRC samples and 1320 noncancerous colorectal tissue controls indicated that KIF14 expression was significantly higher in CRC samples,with an SMD of 1.92(95%CI:1.49-2.35).The area under the curve was 0.94(95%CI:0.92-0.96),with a sensitivity of 0.85(95%CI:0.78-0.90)and a specificity of 0.90(95%CI:0.85-0.93).The positive and negative likelihood ratios were 8.38(95%CI:5.39-13.02)and 0.17(95%CI:0.11-0.26),respectively.At the single-cell level,significant overexpression of KIF14 was observed in CRC cells(P<0.001),with 35 CRC cell lines dependent on KIF14 for growth.The K-M plots demonstrated that KIF14 possesses prognostic value in CRC patients within the GSE71187 and GSE103679 datasets(P<0.05).Binding energy calculations indicated that KIF14 is a potential target for NC(binding energy:10.3 kcal/mol).CONCLUSION KIF14 promotes the growth of CRC cells and acts as an oncogenic factor,potentially serving as a therapeutic target for NC in the treatment of CRC.展开更多
This study aims to develop a chloride diffusion simulation method that considers the hydration microstructure and pore solution properties during the hydration of tricalcium silicate(C3S).The method combines the hydra...This study aims to develop a chloride diffusion simulation method that considers the hydration microstructure and pore solution properties during the hydration of tricalcium silicate(C3S).The method combines the hydration simulation,thermodynamic calculation,and finite element analysis to examine the effects of pore solution,including effect of electrochemical potential,effect of chemical activity,and effect of mechanical interactions between ions,on the chloride effective diffusion coefficient of hydrated C3S paste.The results indicate that the effect of electrochemical potential on chloride diffusion becomes stronger with increasing hydration age due to the increase in the content of hydrated calcium silicate;as the hydration age increases,the effect of chemical activity on chloride diffusion weakens when the number of diffusible elements decreases;the effect of mechanical interactions between ions on chloride diffusion decreases with the increase of hydration age.展开更多
The chloride penetration resistance of cement-based grout materials was improved by nano-silica emulsion.Specimens of mixtures containing different nano-silica particles or emulsions were exposed in sodium chloride so...The chloride penetration resistance of cement-based grout materials was improved by nano-silica emulsion.Specimens of mixtures containing different nano-silica particles or emulsions were exposed in sodium chloride solutions of specific concentrations with different test ages.Hardened properties of the mixes were assessed in terms of weight loss and compressive strength.X-ray diffraction(XRD)and scanning electron microscopy(SEM)of mixes were performed to analysis the phase evolution and microstructure.The results demonstrated that the introduction of nano-SiO_(2) emulsion significantly decreased the compressive strength loss and calcium hydroxide(CH)crystal content of hydration production,and then enhanced the resistance of cement-based grouting materials to chloride ion penetration.This improvement derives from the filling and pozzolanic effects of nano-SiO_(2) particles,which were incorporated via an emulsion and attributed to a well dispersion in grouting matrix.展开更多
Chloride ions(Cl^(-))have been shown to impact the long-lasting nature of reinforced concrete.However,Cl^(-)that are already bound inside the concrete will not lead to the deterioration of the concrete’s characterist...Chloride ions(Cl^(-))have been shown to impact the long-lasting nature of reinforced concrete.However,Cl^(-)that are already bound inside the concrete will not lead to the deterioration of the concrete’s characteristics.The composition of the cement-based material,including the type of cement and auxiliary materials,greatly influences the ability of the material to bind Cl^(-),and varied components result in varying binding beha-vior of the Cl^(-).Simultaneously,the Cl^(-)binding process in concrete is influenced by both the internal and exterior surroundings,as well as the curing practices.These factors impact the hydration process of the cement and the internal pore structure of the concrete.Currently,mathematical theories and molecular dynamics simulations have increasingly been employed as the prevalent methods for examining the binding behaviors of Cl^(-)in concrete.These techniques are extensively utilized for predicting the lifespan and conducting microscopic studies of reinforced concrete in Cl^(-)settings.This work proposes recommendations for future research based on a summary of experimental and simulation investigations on Cl^(-)binding.Which will offer theoretical guidance for studying the binding of Cl^(-)in cement-based materials.展开更多
By using a newly developed 4-hydroxy picolinohydrazide as the ligand,Cu-catalyzed coupling of(hetero)aryl chlorides with sodium aryl sulfonates proceeded smoothly at 130℃to give a series of biarylsulfones in 53%~96%y...By using a newly developed 4-hydroxy picolinohydrazide as the ligand,Cu-catalyzed coupling of(hetero)aryl chlorides with sodium aryl sulfonates proceeded smoothly at 130℃to give a series of biarylsulfones in 53%~96%yields.This represents the first metal-catalyzed coupling reaction of(hetero)aryl chlorides with sodium aryl sulfonates.Aryl and heteroaryl chlorides bearing either electron-donating or electron-withdrawing groups were applicable for this coupling reaction.展开更多
Herein the use of rare-earth compounds in catalytic reduction systems for the end-group functionalization of carboxyl-terminated low-molecularweight fluoropolymers was explored.Leveraging the high catalytic activity a...Herein the use of rare-earth compounds in catalytic reduction systems for the end-group functionalization of carboxyl-terminated low-molecularweight fluoropolymers was explored.Leveraging the high catalytic activity and selectivity of rare-earth compounds along with no residual impact on polymer product's performance,highly efficient catalytic reduction systems containing sodium borohydride(NaBH_(4))and rare-earth chloride(RECl_(3))were specifically designed for a telechelic carboxyl-terminated liquid fluoroeslastomer,aiming to facilitate the conversion of chainend carboxyl groups into hydroxyl groups and improvement in end-group reactivity.To achieve this,lanthanum chloride(LaCl_(3)),cerium chloride(CeCl_(3)),and neodymium chloride(NdCl_(3))were used separately to form catalytic reduction systems with NaBH_(4).The effects of solvent dosage,reaction temperature,reaction time length,and reductant dosage on carboxylic conversion were investigated,and the molecular chain structure,molecular weight,and functional group content of the raw materials and the products were analyzed and characterized by means of infrared spectroscopy(FTIR),proton nuclear magnetic resonance(^(1)H-NMR),fluorine-19 nuclear magnetic resonance(^(19)F-NMR),gel permeation chromatography(GPC),and chemical titration.Moreover,the catalytic activity and selectivity of the rare-earth chlorides,as well as the corresponding underlying interactions were discussed.Results indicated that the rare-earth-containing catalytic reduction systems studied in this work could efficiently convert the chain-end carboxyl groups into highly active hydroxyl groups,with a highest conversion up to 87.0%and differing catalytic reduction activities ranked as NaBH_(4)/CeCl_(3)>NaBH_(4)/LaCl_(3)>NaBH_(4)/NdCl_(3).Compared with the conventional lithium aluminum hydride(LiAIH_(4))reduction system,the NaBH_(4)/RECl_(3)systems provide multiple advantages such as mild reaction conditions,high conversion ratio with good selectivity,and environmental innocuity,and are potentially applicable as new reduction-catalysis combinations for the synthesis and functionalization of polymer materials.展开更多
In the extraction of potassium from salt lakes,Mg is abundant in the form of bischofite(MgCl_(2)·6H_(2)O),which is not utilized effectively,resulting in the waste of resources and environmental pressure.Anhydrous...In the extraction of potassium from salt lakes,Mg is abundant in the form of bischofite(MgCl_(2)·6H_(2)O),which is not utilized effectively,resulting in the waste of resources and environmental pressure.Anhydrous MgCl_(2) prepared by the dehydration of bischofite is a high-quality raw material for the production of Mg.However,direct calcination of MgCl_(2)·6H_(2)O in industrial dehydration processes leads to a large amount of hydrolysis.The by-products are harmful to the electrolysis process of Mg,causing problems such as sludge formation,low current efficiency,and corrosion in the electrodes.To obtain high-purity anhydrous MgCl_(2),different advanced dehydration processes have been proposed.In this review,we focus on the recent progress of the dehydration process.Firstly,we discuss the molecular structure of MgCl_(2)·6H_(2)O and explain the reason why much hydrolysis occurs in dehydration.Secondly,we introduce the specific dehydration processes,mainly divided into direct dehydration processes and indirect dehydration processes.The direct dehydration processes are classified into gas protection heating and molecular sieve dehydration process.Indirect dehydration processes are classified into thermal dehydration of ammonium carnallite(NH_(4)Cl·MgCl_(2)·6H_(2)O),thermal dehydration of potassium carnallite(KCl·MgCl_(2)·6H_(2)O),thermal decomposition of the[HAE]Cl·MgCl_(2)·6H_(2)O,organic solvent distillation,ionic liquid dehydration process and ammonia complexation process.In the meanwhile,purity of anhydrous MgCl_(2) of each dehydration process,as well as the advantages and disadvantages,is discussed.The characteristics of different processes with a simple economic budget are also given in this paper.Finally,the main challenges are evaluated with suggested directions in the future,aiming to guide the synthesis of high-purity anhydrous MgCl_(2).展开更多
The production of C_(2)H_(3)Cl from CH_(3)Cl(MCTV)represents a promising non-petroleum route for synthesizing C_(2)alkenes from C_(1)molecules.Exploration of new MCTV catalysts is crucial for advancing sustainable che...The production of C_(2)H_(3)Cl from CH_(3)Cl(MCTV)represents a promising non-petroleum route for synthesizing C_(2)alkenes from C_(1)molecules.Exploration of new MCTV catalysts is crucial for advancing sustainable chemical production.In this study,we present NaVO_(3)as a surface-confined coupling center for·CH_(2)Cl radicals,demonstrating its superior performance in the selective coupling of methyl chloride to synthesize vinyl chloride.By incorporating NaVO_(3)onto the surface of CeO_(2),the catalyst enables effective capture of·CH_(2)Cl radicals during the CH_(3)Cl oxidative pyrolysis and their subsequent conversion into C_(2)H_(3)Cl.We experimentally validate the capability of highly dispersed Na-VO_(3)to controllably couple·CH_(2)Cl radicals through in-situ synchrotron-based vacuum ultraviolet photoionization mass spectrometry.The results demonstrate that the dispersion of NaVO_(3)on the catalyst surface has a considerable impact on the reaction efficiency of·CH_(2)Cl radicals and the overall MCTV performance.This discovery holds substantial implications for the controlled C_(1)radical transformation and provides a guidance for the design of catalysts for sustainable production of C_(2)H_(3)Cl.展开更多
In this study,synthetic wastewater containing 110μg/L arsenate(As(V)),0-20 mg/L fulvic acid(FA),and 0-12.3 mg/L phosphate was treated with 3 mg/L Fe3+.The mechanisms of FA and phosphate effects on As(V)removal by fer...In this study,synthetic wastewater containing 110μg/L arsenate(As(V)),0-20 mg/L fulvic acid(FA),and 0-12.3 mg/L phosphate was treated with 3 mg/L Fe3+.The mechanisms of FA and phosphate effects on As(V)removal by ferric chloride were determined using 0.22-10μm pore-size filtration,Zetasizer analysis,and in situ flow through cell ATR-FTIR.The results showed that up to 20mg/L FA had almost no effect on the solubility of ferric hydroxide precipitates and adsorption of As(V)by the precipitates.When FA concentration increased from 0 to 20 mg/L,the adsorption of FA led to higher negative zeta potential of the precipitates and the strong electrostatic repulsion between the precipitates decreased the particle size of ferric hydroxide flocs fromlarger than 10μmto smaller than 1μm.In the presence of 5-20 mg/L FA,46%-63%As(V)was adsorbed onto the flocs with particle size in the range of 0.45-1μm.On the other hand,phosphate did not affect the size of ferric hydroxide flocs and significantly increased the dissolved As(V)concentration because it competed with As(V)for adsorption sites on ferric hydroxide precipitates.The addition of 5mg/L cationic organic flocculant significantly reduced the effect of FA on As(V)removal,but did not reduce the effect of phosphate on As(V)removal.The findings of this study will help develop effective arsenic treatment techniques and predict the mobility of arsenic in the environment.展开更多
This minireview explores the role of acetylcholine and muscarinic receptors in the pathophysiology of schizophrenia and summarizes the latest data on xanomeline/trospium chloride,a novel antipsychotic approved by the ...This minireview explores the role of acetylcholine and muscarinic receptors in the pathophysiology of schizophrenia and summarizes the latest data on xanomeline/trospium chloride,a novel antipsychotic approved by the United States Food and Drug Administration in September 2024.Evidence suggests that cholinergic dysfunction,particularly an imbalance in the expression of the M1 and M4 muscarinic receptors,may contribute to the pathophysiology and symptoms of schizophrenia.Xanomeline/trospium chloride combines xanomeline,an M1 and M4 receptor agonist,with trospium chloride,a non-selective peripheral muscarinic receptor antagonist that reduces peripheral cholinergic side effects.Clinical trials have demonstrated significant reductions in the positive and negative symptoms of schizophrenia,with improvements in Positive and Negati-ve Syndrome Scale scores observed as early as two weeks.A post-hoc analysis of one trial revealed cognitive improvements in patients with baseline cognitive impairment.This medication was generally well-tolerated,with mild-to-moderate gastrointestinal symptoms being the most common adverse events.While these results are promising,further research is needed to better understand its effectiveness and safety in real-world clinical practice,and to define its optimal role in managing this complex psychiatric disorder.展开更多
Salinity tissue tolerance is a key trait that confers adaptive potential in halophytic species.The aim of this study was to understand the mechanistic basis of salinity tissue tolerance in the Oryza coarctata,a haloph...Salinity tissue tolerance is a key trait that confers adaptive potential in halophytic species.The aim of this study was to understand the mechanistic basis of salinity tissue tolerance in the Oryza coarctata,a halophytic wild relative of cultivated rice Oryza sativa,to be then used as novel targets for improving salinity stress tolerance of O.sativa.Salinity led to ~80% decline in mesophyll cell viability in cultivated rice,whereas only 15% reduction was observed in the wild rice.In response to NaCl treatments,mesophyll cells of O.coarctata showed less Na^(+) uptake and better K^(+) retention than cultivated rice.Pharmacological experiments suggested that salinity-induced Na^(+) uptake and K^(+) loss in O.coarctata were mediated by non-selective cation channels(NSCCs) while K^(+) loss in cultivated rice was mediated predominantly by GORK(guard cell outward-rectifying K^(+)) channels.Salt treatment resulted in a depolarization of the plasma membrane(PM) in O.sativa.In contrast,O.coarctata had NaCl dose-dependent hyperpolarization in the mesophyll cells,due to its higher preference for Cl^(-)uptake.This difference in plant ionic relations was partially attributable to differences in transcriptional expression levels of Potassium transporter 1(AKT1),Salt overly sensitive 1(SOS1),Sodium transporter OsHKT1;4,and Chloride channel(OsCLC1).It is concluded that O.coarctata possesses a strong ability to discriminate between Cl^(-)and Na^(+) uptake(a trait lacking in cultivated rice) and use it to maintain negative membrane potential(MP) values without activating H^(+)-ATPase,thus enabling more efficient K^(+) retention in mesophyll with low energy costs.The above traits should be considered as potential targets in the rice breeding program for salt tolerance enhancement.展开更多
Direct electrolysis of seawater offers a transformative technology for sustainable hydrogen production,circumventing the constraint of freshwater scarcity.However,the serious electrode corrosion and competitive chlori...Direct electrolysis of seawater offers a transformative technology for sustainable hydrogen production,circumventing the constraint of freshwater scarcity.However,the serious electrode corrosion and competitive chloride oxidation reactions make oxygen evolution reaction(OER)in seawater extremely challenging.Herein,the low-cost and scalable CoFe layered double hydroxides with Cl^(-)intercalation and decorated with Ce(OH)_(3)(named as CoFe-Cl^(-)/Ce(OH)_(3))catalyst is synthesized via rapid electrodeposition under ambient conditions,which is quickly reconstructed into a CeO_(2)decorated and Cl^(-)intercalated CoFeOOH(CoFeOOH-Cl^(-)/CeO_(2))during OER.Theoretical investigation reveals that Cl^(-)intercalation weakens the adsorption ability of Cl^(-)on Co/Fe atoms and hinders unfavorable coupling with chloride,thereby preventing the chlorine corrosion process and enhancing catalytic stability and activity.The CeO_(2)with hard Lewis acidity preferentially binds to OH-with harder Lewis base to ensure the OH-rich microenvironment around catalyst even under high current operating conditions,thus further enhancing stability and improving OER activity.The functionalized CoFe-Cl^(-)/Ce(OH)_(3)delivers 1000 mA cm^(-2)current density at only 329 mV overpotential with excellent stability for 1000 h under alkaline seawater.Electrochemical experiments elucidate the OER catalytic mechanism in which CeO_(2)serves as a co-catalyst for enriching OH-and CoFeOOH-Cl^(-)is the active species.Our work is a substantial step towards achieving massive and sustainable production of hydrogen fuel from immense seawater.展开更多
Designing xerogels at the molecular level to overcome volume shrinkage is a promising strategy for carbon xerogels with desirable structure and performance.Here,we design a xerogel with non-shrinkage by introducing Zn...Designing xerogels at the molecular level to overcome volume shrinkage is a promising strategy for carbon xerogels with desirable structure and performance.Here,we design a xerogel with non-shrinkage by introducing ZnCl_(2) into resorcinol-melamine-formaldehyde polymerization.The gel network consisting of micrometer pores and large particles(0.26-1.35μm)is constructed by the coordination of Zn^(2+) with oxygen/nitrogen-containing groups,which is attributed to the structural support of the rigid triazine skeleton with large steric hindrance.Therefore,the reinforced gel network possesses enough strength to withstand capillary forces during atmospheric drying,and special drying and solvent exchange are avoided.The xerogels show non-shrinkage and a short preparation time of 24 h.The resulted activated carbon xerogels with interconnected hierarchically micro-meso-macropores exhibit an optimal specific surface area of 1520 m^(2)/g(through xerogels pyrolysis and the pore-forming of ZnCl_(2)),high adsorption(methylene blue,I-,Cu^(2+),etc.),and repeated adsorption ability.This work provides novel thought for porous nanomaterials with non-shrinkage and desirable structures in adsorption and energy storage.展开更多
Growth of high-quality Nb_(3)Sn thin films for superconducting radiofrequency(SRF)applications using the vapor diffusion method requires a uniform distribution of tin nuclei on the niobium(Nb)surface.This study examin...Growth of high-quality Nb_(3)Sn thin films for superconducting radiofrequency(SRF)applications using the vapor diffusion method requires a uniform distribution of tin nuclei on the niobium(Nb)surface.This study examines the mechanism underlying the observed non-uniform distribution of tin nuclei with tin chloride SnCl_(2).Electron backscatter diffraction(EBSD)analysis was used to examine the correlation between the nucleation behavior and orientation of niobium grains in the substrate.The findings of the density functional theory(DFT)simulation are in good agreement with the experimental results,showing that the non-uniform distribution of tin nuclei is the result of the adsorption energy of SnCl_(2)molecules by varied niobium grain orientations.Further analysis indicated that the surface roughness and grain size of niobium also played significant roles in the nucleation behavior.This study provides valuable insights into enhancing the surface pretreatment of niobium substrates during the growth of Nb_(3)Sn thin films using the vapor diffusion method.展开更多
The authors regret that in 1.2.Instruments section of the article,when describing the principle of TiH300,the original content of“Briefly,ambient HONO was first absorbed by deionized water in a two-channel stripping ...The authors regret that in 1.2.Instruments section of the article,when describing the principle of TiH300,the original content of“Briefly,ambient HONO was first absorbed by deionized water in a two-channel stripping coil.The absorbed liquid nitrite was mixed with sulfanilamide,N-(1-naphthyl)-ethylenediamine dihydrochloride,and hydrogen chloride solution to form the azo dye derivative.”展开更多
Contamination of microplastics(MPs)and their associated plastic additives in the marine environment is a global concern due to their widespread distribution and toxicity to aquatic life.Although polyvinyl chloride(PVC...Contamination of microplastics(MPs)and their associated plastic additives in the marine environment is a global concern due to their widespread distribution and toxicity to aquatic life.Although polyvinyl chloride(PVC)materials are commonly used in aquaculture environments,the potential risks of PVC MPs and the release of their additives in aquatic environments and organisms remain largely unknown.In this study,we investigated the leaching behaviors of phthalate esters(PAEs),including the mass and composition of PAEs in PVC MPs and their leaching kinetics,and evaluated the environmental risks of using PVC canvas in aquaculture activities.It was found that diethyl phthalate(DEP)was the most dominant PAE compound leached from PVC MPs(44.70±7.87 ng/g),followed by dimethyl phthalate(DMP,24.40±1.56 ng/g).The Elovich model was applied to simulate the leaching kinetics,and the simulated curves showed similar logarithmic trends that PAEs rapidly migrated from MPs to the water column at first and followed by a gradual increase over time.The different leaching kinetics of PAEs can be explained by their chemical properties,such as water solubility,molecular weight,and octanol-water partition coefficient.Compounds with lower solubility showed higher leaching coefficients,which are the constants of different PAEs in Elovich equation.Considering the potential joint toxicity of PVC leachates and the importance of food security,it is recommended to use PVC products responsibly and manage plastic waste properly.展开更多
The adsorption properties of a magnesium porphyrin(MgP)molecule on Au(111)surface covered with up to three lay-ers of sodium chloride(NaCl)were investigated by means of first-principles calculations.The most stable ad...The adsorption properties of a magnesium porphyrin(MgP)molecule on Au(111)surface covered with up to three lay-ers of sodium chloride(NaCl)were investigated by means of first-principles calculations.The most stable adsorption configuration of MgP on the NaCl/Au(111)heterosurfaces was found to be at the Cl-top site with a 20°angle between the[110]lattice direction of NaCl and the Mg–N bond of the molecule.Compared with MgP molecule adsorbed on bare Au(111),the inclusion of NaCl lay-ers can lead to a significant decrease in the adsorption energy of the MgP molecule.The exis-tence of NaCl layers also reduced the charge transfer between the molecule and the surface.For heterosurfaces with two or three monolayers of NaCl,the charge transfer was almost com-pletely suppressed.The obtained partial density of states(PDOS)showed that hybridization between the electronic structures of the adsorbed MgP molecule and the metal surface can be significantly suppressed when NaCl layers were added.For the heterosurface with three lay-ers of NaCl,the PDOS around the Fermi level was almost identical with that of the free molecule,suggesting the electronic structure of the MgP molecule was nicely preserved.Influ-ence of the NaCl layers on the electronic structure of the MgP molecule was mainly found for molecular orbitals(MOs)away from the Fermi level as a result of the large band gap of the NaCl layers.展开更多
文摘Patients with advanced liver cirrhosis and liver failure frequently experience abnormalities in their serum electrolyte levels.In such patients,hyponatremia has been identified as a predictor of poor outcomes.However,emerging evidence suggests that serum chloride may provide even better prognostic information in similar situations.Hypochloremia,characterised by low serum chloride levels,has been linked to increased mortality,exacerbated organ dysfunction,and higher requirements for renal replacement therapy and vasopressors in various critical conditions,including advanced liver diseases.The pathophysiological mecha-nisms underlying the association between low serum chloride levels and poor outcomes in liver disease appear to involve complex interactions among electro-lyte imbalances,renal function,and systemic hemodynamics.Chloride dysregu-lation can influence renal salt-sensing mechanisms,disrupt acid-base homeostasis,and exacerbate complications such as hepatic encephalopathy and hepatorenal syndrome.This article aims to elucidate the prognostic significance of lower serum chloride levels in patients with advanced liver disease.By reviewing recent literature and analysing clinical data,we seek to establish serum chloride as an underutilised but valuable prognostic marker.Understanding the role of serum chloride in liver disease could enhance prognostic accuracy,refine treatment strategies,and ultimately improve patient outcomes.
基金supported by the research projects AP23486880 from the Ministry of Higher EducationScience of the Republic of Kazakhstan and 111024CRP2010,20122022FD4135 from Nazarbayev University.
文摘Recycling plastic waste into triboelectric nanogenerators(TENGs)presents a sustainable approach to energy harvesting,self-powered sensing,and environmental remediation.This study investigates the recycling of polyvinyl chloride(PVC)pipe waste polymers into nanofibers(NFs)optimized for TENG applications.We focused on optimizing the morphology of recycled PVC polymer to NFs and enhancing their piezoelectric properties by incorporating ZnO nanoparticles(NPs).The optimized PVC/0.5 wt%ZnO NFs were tested with Nylon-6 NFs,and copper(Cu)electrodes.The Nylon-6 NFs exhibited a power density of 726.3μWcm^(-2)—1.13 times higher than Cu and maintained 90%stability after 172800 cycles,successfully powering various colored LEDs.Additionally,a 3D-designed device was developed to harvest energy from biomechanical movements such as finger tapping,hand tapping,and foot pressing,making it suitable for wearable energy harvesting,automatic switches,and invisible sensors in surveillance systems.This study demonstrates that recycling polymers for TENG devices can effectively address energy,sensor,and environmental challenges.
基金Natural Science Foundation of Shandong Province,No.ZR2020QH185Scientific Research Nurturing Fund of The First Affiliated Hospital of Shandong First Medical University&Shandong Provincial Qianfoshan Hospital,No.QYPY2020NSFC0803+2 种基金Guangxi Zhuang Autonomous Region Health Commission Scientific Research Project,No.Z-A20220415Guangxi Medical University Teacher Teaching Ability Development Project,No.2022JFA02Guangxi Medical University Undergraduate Education and Teaching Reform Project,No.2023Y05.
文摘BACKGROUND Colorectal cancer(CRC)is the third most common cancer globally,causing over 900000 deaths annually.Risk factors include aging,diet,obesity,sedentary lifestyle,tobacco use,genetic predisposition,and inflammatory bowel disease.Despite current treatments,survival rates for advanced CRC remain low,highlighting the need for better therapeutic strategies.AIM To evaluate both the clinical significance and the pathological implications of the Kinesin family member 14(KIF14)expression within CRC specimens.Additionally,this study aims to investigate the interaction between nitidine chloride(NC)and KIF14,considering their potential as therapeutic targets.METHODS The expression of the KIF14 protein in CRC was analyzed using immunohistochemical staining.The integration of multicenter high-throughput data facilitated the calculation of the standardized mean difference(SMD)for KIF14 mRNA levels.The assessment of clinical and pathological impact was enhanced by analyzing combined receiver operating characteristic curves,along with measures of sensitivity,specificity,and likelihood ratios.Additionally,clustered regularly interspaced short palindromic repeats knockout screening for cell growth and single-cell sequencing were employed to validate the significance of KIF14 expression in CRC.Survival analysis established the prognostic value of KIF14 in CRC.The molecular mechanism of NC against CRC was elucidated through whole-genome sequencing and enrichment analysis,and molecular docking was utilized to explore the targeting affinity between NC and KIF14.RESULTS KIF14 was highly expressed in 208 CRC patients.Data from 17 platforms involving 2436 CRC samples and 1320 noncancerous colorectal tissue controls indicated that KIF14 expression was significantly higher in CRC samples,with an SMD of 1.92(95%CI:1.49-2.35).The area under the curve was 0.94(95%CI:0.92-0.96),with a sensitivity of 0.85(95%CI:0.78-0.90)and a specificity of 0.90(95%CI:0.85-0.93).The positive and negative likelihood ratios were 8.38(95%CI:5.39-13.02)and 0.17(95%CI:0.11-0.26),respectively.At the single-cell level,significant overexpression of KIF14 was observed in CRC cells(P<0.001),with 35 CRC cell lines dependent on KIF14 for growth.The K-M plots demonstrated that KIF14 possesses prognostic value in CRC patients within the GSE71187 and GSE103679 datasets(P<0.05).Binding energy calculations indicated that KIF14 is a potential target for NC(binding energy:10.3 kcal/mol).CONCLUSION KIF14 promotes the growth of CRC cells and acts as an oncogenic factor,potentially serving as a therapeutic target for NC in the treatment of CRC.
基金Funded by the Natural Science Foundation of Jiangsu Province(No.BK20241529)China Postdoctoral Science Foundation(No.2024M750736)。
文摘This study aims to develop a chloride diffusion simulation method that considers the hydration microstructure and pore solution properties during the hydration of tricalcium silicate(C3S).The method combines the hydration simulation,thermodynamic calculation,and finite element analysis to examine the effects of pore solution,including effect of electrochemical potential,effect of chemical activity,and effect of mechanical interactions between ions,on the chloride effective diffusion coefficient of hydrated C3S paste.The results indicate that the effect of electrochemical potential on chloride diffusion becomes stronger with increasing hydration age due to the increase in the content of hydrated calcium silicate;as the hydration age increases,the effect of chemical activity on chloride diffusion weakens when the number of diffusible elements decreases;the effect of mechanical interactions between ions on chloride diffusion decreases with the increase of hydration age.
基金Funded by a Science and Technology Project from the Ministry of Housing and Urban-Rural Development of the People’s Republic of China(No.2019-K-047)Yangzhou Government-Yangzhou University Cooperative Platform Project for Science and Technology Innovation(No.YZ2020262)。
文摘The chloride penetration resistance of cement-based grout materials was improved by nano-silica emulsion.Specimens of mixtures containing different nano-silica particles or emulsions were exposed in sodium chloride solutions of specific concentrations with different test ages.Hardened properties of the mixes were assessed in terms of weight loss and compressive strength.X-ray diffraction(XRD)and scanning electron microscopy(SEM)of mixes were performed to analysis the phase evolution and microstructure.The results demonstrated that the introduction of nano-SiO_(2) emulsion significantly decreased the compressive strength loss and calcium hydroxide(CH)crystal content of hydration production,and then enhanced the resistance of cement-based grouting materials to chloride ion penetration.This improvement derives from the filling and pozzolanic effects of nano-SiO_(2) particles,which were incorporated via an emulsion and attributed to a well dispersion in grouting matrix.
文摘Chloride ions(Cl^(-))have been shown to impact the long-lasting nature of reinforced concrete.However,Cl^(-)that are already bound inside the concrete will not lead to the deterioration of the concrete’s characteristics.The composition of the cement-based material,including the type of cement and auxiliary materials,greatly influences the ability of the material to bind Cl^(-),and varied components result in varying binding beha-vior of the Cl^(-).Simultaneously,the Cl^(-)binding process in concrete is influenced by both the internal and exterior surroundings,as well as the curing practices.These factors impact the hydration process of the cement and the internal pore structure of the concrete.Currently,mathematical theories and molecular dynamics simulations have increasingly been employed as the prevalent methods for examining the binding behaviors of Cl^(-)in concrete.These techniques are extensively utilized for predicting the lifespan and conducting microscopic studies of reinforced concrete in Cl^(-)settings.This work proposes recommendations for future research based on a summary of experimental and simulation investigations on Cl^(-)binding.Which will offer theoretical guidance for studying the binding of Cl^(-)in cement-based materials.
文摘By using a newly developed 4-hydroxy picolinohydrazide as the ligand,Cu-catalyzed coupling of(hetero)aryl chlorides with sodium aryl sulfonates proceeded smoothly at 130℃to give a series of biarylsulfones in 53%~96%yields.This represents the first metal-catalyzed coupling reaction of(hetero)aryl chlorides with sodium aryl sulfonates.Aryl and heteroaryl chlorides bearing either electron-donating or electron-withdrawing groups were applicable for this coupling reaction.
文摘Herein the use of rare-earth compounds in catalytic reduction systems for the end-group functionalization of carboxyl-terminated low-molecularweight fluoropolymers was explored.Leveraging the high catalytic activity and selectivity of rare-earth compounds along with no residual impact on polymer product's performance,highly efficient catalytic reduction systems containing sodium borohydride(NaBH_(4))and rare-earth chloride(RECl_(3))were specifically designed for a telechelic carboxyl-terminated liquid fluoroeslastomer,aiming to facilitate the conversion of chainend carboxyl groups into hydroxyl groups and improvement in end-group reactivity.To achieve this,lanthanum chloride(LaCl_(3)),cerium chloride(CeCl_(3)),and neodymium chloride(NdCl_(3))were used separately to form catalytic reduction systems with NaBH_(4).The effects of solvent dosage,reaction temperature,reaction time length,and reductant dosage on carboxylic conversion were investigated,and the molecular chain structure,molecular weight,and functional group content of the raw materials and the products were analyzed and characterized by means of infrared spectroscopy(FTIR),proton nuclear magnetic resonance(^(1)H-NMR),fluorine-19 nuclear magnetic resonance(^(19)F-NMR),gel permeation chromatography(GPC),and chemical titration.Moreover,the catalytic activity and selectivity of the rare-earth chlorides,as well as the corresponding underlying interactions were discussed.Results indicated that the rare-earth-containing catalytic reduction systems studied in this work could efficiently convert the chain-end carboxyl groups into highly active hydroxyl groups,with a highest conversion up to 87.0%and differing catalytic reduction activities ranked as NaBH_(4)/CeCl_(3)>NaBH_(4)/LaCl_(3)>NaBH_(4)/NdCl_(3).Compared with the conventional lithium aluminum hydride(LiAIH_(4))reduction system,the NaBH_(4)/RECl_(3)systems provide multiple advantages such as mild reaction conditions,high conversion ratio with good selectivity,and environmental innocuity,and are potentially applicable as new reduction-catalysis combinations for the synthesis and functionalization of polymer materials.
基金funded by Natural Science Foundation of Xinjiang Uygur Autonomous Region(2022D01F60)Tianshan Talents Plan of Xinjiang Uygur Autonomous Region(2022TSYCJC0001)+2 种基金National Natural Science Foundation of China(22368051)Science and Technology Plan Project of Karamay(20232023hjcxrc0038 and 2024hjcxrc0118)Projects of Talents Recruitment of GDUPT(2023rcyj2005)。
文摘In the extraction of potassium from salt lakes,Mg is abundant in the form of bischofite(MgCl_(2)·6H_(2)O),which is not utilized effectively,resulting in the waste of resources and environmental pressure.Anhydrous MgCl_(2) prepared by the dehydration of bischofite is a high-quality raw material for the production of Mg.However,direct calcination of MgCl_(2)·6H_(2)O in industrial dehydration processes leads to a large amount of hydrolysis.The by-products are harmful to the electrolysis process of Mg,causing problems such as sludge formation,low current efficiency,and corrosion in the electrodes.To obtain high-purity anhydrous MgCl_(2),different advanced dehydration processes have been proposed.In this review,we focus on the recent progress of the dehydration process.Firstly,we discuss the molecular structure of MgCl_(2)·6H_(2)O and explain the reason why much hydrolysis occurs in dehydration.Secondly,we introduce the specific dehydration processes,mainly divided into direct dehydration processes and indirect dehydration processes.The direct dehydration processes are classified into gas protection heating and molecular sieve dehydration process.Indirect dehydration processes are classified into thermal dehydration of ammonium carnallite(NH_(4)Cl·MgCl_(2)·6H_(2)O),thermal dehydration of potassium carnallite(KCl·MgCl_(2)·6H_(2)O),thermal decomposition of the[HAE]Cl·MgCl_(2)·6H_(2)O,organic solvent distillation,ionic liquid dehydration process and ammonia complexation process.In the meanwhile,purity of anhydrous MgCl_(2) of each dehydration process,as well as the advantages and disadvantages,is discussed.The characteristics of different processes with a simple economic budget are also given in this paper.Finally,the main challenges are evaluated with suggested directions in the future,aiming to guide the synthesis of high-purity anhydrous MgCl_(2).
文摘The production of C_(2)H_(3)Cl from CH_(3)Cl(MCTV)represents a promising non-petroleum route for synthesizing C_(2)alkenes from C_(1)molecules.Exploration of new MCTV catalysts is crucial for advancing sustainable chemical production.In this study,we present NaVO_(3)as a surface-confined coupling center for·CH_(2)Cl radicals,demonstrating its superior performance in the selective coupling of methyl chloride to synthesize vinyl chloride.By incorporating NaVO_(3)onto the surface of CeO_(2),the catalyst enables effective capture of·CH_(2)Cl radicals during the CH_(3)Cl oxidative pyrolysis and their subsequent conversion into C_(2)H_(3)Cl.We experimentally validate the capability of highly dispersed Na-VO_(3)to controllably couple·CH_(2)Cl radicals through in-situ synchrotron-based vacuum ultraviolet photoionization mass spectrometry.The results demonstrate that the dispersion of NaVO_(3)on the catalyst surface has a considerable impact on the reaction efficiency of·CH_(2)Cl radicals and the overall MCTV performance.This discovery holds substantial implications for the controlled C_(1)radical transformation and provides a guidance for the design of catalysts for sustainable production of C_(2)H_(3)Cl.
基金financially supported by the New Jersey Department of Environmental ProtectionUS EPA。
文摘In this study,synthetic wastewater containing 110μg/L arsenate(As(V)),0-20 mg/L fulvic acid(FA),and 0-12.3 mg/L phosphate was treated with 3 mg/L Fe3+.The mechanisms of FA and phosphate effects on As(V)removal by ferric chloride were determined using 0.22-10μm pore-size filtration,Zetasizer analysis,and in situ flow through cell ATR-FTIR.The results showed that up to 20mg/L FA had almost no effect on the solubility of ferric hydroxide precipitates and adsorption of As(V)by the precipitates.When FA concentration increased from 0 to 20 mg/L,the adsorption of FA led to higher negative zeta potential of the precipitates and the strong electrostatic repulsion between the precipitates decreased the particle size of ferric hydroxide flocs fromlarger than 10μmto smaller than 1μm.In the presence of 5-20 mg/L FA,46%-63%As(V)was adsorbed onto the flocs with particle size in the range of 0.45-1μm.On the other hand,phosphate did not affect the size of ferric hydroxide flocs and significantly increased the dissolved As(V)concentration because it competed with As(V)for adsorption sites on ferric hydroxide precipitates.The addition of 5mg/L cationic organic flocculant significantly reduced the effect of FA on As(V)removal,but did not reduce the effect of phosphate on As(V)removal.The findings of this study will help develop effective arsenic treatment techniques and predict the mobility of arsenic in the environment.
文摘This minireview explores the role of acetylcholine and muscarinic receptors in the pathophysiology of schizophrenia and summarizes the latest data on xanomeline/trospium chloride,a novel antipsychotic approved by the United States Food and Drug Administration in September 2024.Evidence suggests that cholinergic dysfunction,particularly an imbalance in the expression of the M1 and M4 muscarinic receptors,may contribute to the pathophysiology and symptoms of schizophrenia.Xanomeline/trospium chloride combines xanomeline,an M1 and M4 receptor agonist,with trospium chloride,a non-selective peripheral muscarinic receptor antagonist that reduces peripheral cholinergic side effects.Clinical trials have demonstrated significant reductions in the positive and negative symptoms of schizophrenia,with improvements in Positive and Negati-ve Syndrome Scale scores observed as early as two weeks.A post-hoc analysis of one trial revealed cognitive improvements in patients with baseline cognitive impairment.This medication was generally well-tolerated,with mild-to-moderate gastrointestinal symptoms being the most common adverse events.While these results are promising,further research is needed to better understand its effectiveness and safety in real-world clinical practice,and to define its optimal role in managing this complex psychiatric disorder.
基金supported by the Australian Department of Industry, Innovation and Science (Project AISRF48490) grantIndo-Australian Biotechnology Fund (BT/Indo-Aus/09/03/2015) provided by the Department of Biotechnology, Government of India。
文摘Salinity tissue tolerance is a key trait that confers adaptive potential in halophytic species.The aim of this study was to understand the mechanistic basis of salinity tissue tolerance in the Oryza coarctata,a halophytic wild relative of cultivated rice Oryza sativa,to be then used as novel targets for improving salinity stress tolerance of O.sativa.Salinity led to ~80% decline in mesophyll cell viability in cultivated rice,whereas only 15% reduction was observed in the wild rice.In response to NaCl treatments,mesophyll cells of O.coarctata showed less Na^(+) uptake and better K^(+) retention than cultivated rice.Pharmacological experiments suggested that salinity-induced Na^(+) uptake and K^(+) loss in O.coarctata were mediated by non-selective cation channels(NSCCs) while K^(+) loss in cultivated rice was mediated predominantly by GORK(guard cell outward-rectifying K^(+)) channels.Salt treatment resulted in a depolarization of the plasma membrane(PM) in O.sativa.In contrast,O.coarctata had NaCl dose-dependent hyperpolarization in the mesophyll cells,due to its higher preference for Cl^(-)uptake.This difference in plant ionic relations was partially attributable to differences in transcriptional expression levels of Potassium transporter 1(AKT1),Salt overly sensitive 1(SOS1),Sodium transporter OsHKT1;4,and Chloride channel(OsCLC1).It is concluded that O.coarctata possesses a strong ability to discriminate between Cl^(-)and Na^(+) uptake(a trait lacking in cultivated rice) and use it to maintain negative membrane potential(MP) values without activating H^(+)-ATPase,thus enabling more efficient K^(+) retention in mesophyll with low energy costs.The above traits should be considered as potential targets in the rice breeding program for salt tolerance enhancement.
基金financial support from the National Natural Science Foundation of China(52372173,52072034)。
文摘Direct electrolysis of seawater offers a transformative technology for sustainable hydrogen production,circumventing the constraint of freshwater scarcity.However,the serious electrode corrosion and competitive chloride oxidation reactions make oxygen evolution reaction(OER)in seawater extremely challenging.Herein,the low-cost and scalable CoFe layered double hydroxides with Cl^(-)intercalation and decorated with Ce(OH)_(3)(named as CoFe-Cl^(-)/Ce(OH)_(3))catalyst is synthesized via rapid electrodeposition under ambient conditions,which is quickly reconstructed into a CeO_(2)decorated and Cl^(-)intercalated CoFeOOH(CoFeOOH-Cl^(-)/CeO_(2))during OER.Theoretical investigation reveals that Cl^(-)intercalation weakens the adsorption ability of Cl^(-)on Co/Fe atoms and hinders unfavorable coupling with chloride,thereby preventing the chlorine corrosion process and enhancing catalytic stability and activity.The CeO_(2)with hard Lewis acidity preferentially binds to OH-with harder Lewis base to ensure the OH-rich microenvironment around catalyst even under high current operating conditions,thus further enhancing stability and improving OER activity.The functionalized CoFe-Cl^(-)/Ce(OH)_(3)delivers 1000 mA cm^(-2)current density at only 329 mV overpotential with excellent stability for 1000 h under alkaline seawater.Electrochemical experiments elucidate the OER catalytic mechanism in which CeO_(2)serves as a co-catalyst for enriching OH-and CoFeOOH-Cl^(-)is the active species.Our work is a substantial step towards achieving massive and sustainable production of hydrogen fuel from immense seawater.
基金supported by the National Key Research and Development Program of China(No.2023YFB3711501)the Shanghai Industrial Collaborative Innovation Leading Group Office(No.XTCX-KJ-2023-53)+3 种基金the Fundamental Research Funds for the Central Universities(No.23D110609)the Open Research Fund of Songshan Lake Materials Laboratory(No.2022SLABFN09)the Foundation of State Key Laboratory of Biobased Material and Green Paper-making,Qilu University of Technology,Shandong Academy of Sciences(No.GZKF202231)the Fundamental Research Funds for the Central Universities and Graduate Student Innovation Fund of Donghua University(No.CUSF-DH-d-2022012).
文摘Designing xerogels at the molecular level to overcome volume shrinkage is a promising strategy for carbon xerogels with desirable structure and performance.Here,we design a xerogel with non-shrinkage by introducing ZnCl_(2) into resorcinol-melamine-formaldehyde polymerization.The gel network consisting of micrometer pores and large particles(0.26-1.35μm)is constructed by the coordination of Zn^(2+) with oxygen/nitrogen-containing groups,which is attributed to the structural support of the rigid triazine skeleton with large steric hindrance.Therefore,the reinforced gel network possesses enough strength to withstand capillary forces during atmospheric drying,and special drying and solvent exchange are avoided.The xerogels show non-shrinkage and a short preparation time of 24 h.The resulted activated carbon xerogels with interconnected hierarchically micro-meso-macropores exhibit an optimal specific surface area of 1520 m^(2)/g(through xerogels pyrolysis and the pore-forming of ZnCl_(2)),high adsorption(methylene blue,I-,Cu^(2+),etc.),and repeated adsorption ability.This work provides novel thought for porous nanomaterials with non-shrinkage and desirable structures in adsorption and energy storage.
基金supported by the National Natural Science Foundation of China(No.12175283)Youth Innovation Promotion Association of Chinese Academy of Sciences(2020410)Advanced Energy Science and Technology Guangdong Laboratory(HND20TDSPCD,HND22PTDZD).
文摘Growth of high-quality Nb_(3)Sn thin films for superconducting radiofrequency(SRF)applications using the vapor diffusion method requires a uniform distribution of tin nuclei on the niobium(Nb)surface.This study examines the mechanism underlying the observed non-uniform distribution of tin nuclei with tin chloride SnCl_(2).Electron backscatter diffraction(EBSD)analysis was used to examine the correlation between the nucleation behavior and orientation of niobium grains in the substrate.The findings of the density functional theory(DFT)simulation are in good agreement with the experimental results,showing that the non-uniform distribution of tin nuclei is the result of the adsorption energy of SnCl_(2)molecules by varied niobium grain orientations.Further analysis indicated that the surface roughness and grain size of niobium also played significant roles in the nucleation behavior.This study provides valuable insights into enhancing the surface pretreatment of niobium substrates during the growth of Nb_(3)Sn thin films using the vapor diffusion method.
文摘The authors regret that in 1.2.Instruments section of the article,when describing the principle of TiH300,the original content of“Briefly,ambient HONO was first absorbed by deionized water in a two-channel stripping coil.The absorbed liquid nitrite was mixed with sulfanilamide,N-(1-naphthyl)-ethylenediamine dihydrochloride,and hydrogen chloride solution to form the azo dye derivative.”
基金Supported by the State Key Laboratory of Marine Pollution(SKLMP)in City University of Hong Kong,the Shenzhen Science and Technology Program(No.JCYJ20220530140813030 to Meng YAN)the Innovation and Technology Commission(ITC)of the Hong Kong SAR Government(No.9448002),which provides regular research funding support to SKLMP。
文摘Contamination of microplastics(MPs)and their associated plastic additives in the marine environment is a global concern due to their widespread distribution and toxicity to aquatic life.Although polyvinyl chloride(PVC)materials are commonly used in aquaculture environments,the potential risks of PVC MPs and the release of their additives in aquatic environments and organisms remain largely unknown.In this study,we investigated the leaching behaviors of phthalate esters(PAEs),including the mass and composition of PAEs in PVC MPs and their leaching kinetics,and evaluated the environmental risks of using PVC canvas in aquaculture activities.It was found that diethyl phthalate(DEP)was the most dominant PAE compound leached from PVC MPs(44.70±7.87 ng/g),followed by dimethyl phthalate(DMP,24.40±1.56 ng/g).The Elovich model was applied to simulate the leaching kinetics,and the simulated curves showed similar logarithmic trends that PAEs rapidly migrated from MPs to the water column at first and followed by a gradual increase over time.The different leaching kinetics of PAEs can be explained by their chemical properties,such as water solubility,molecular weight,and octanol-water partition coefficient.Compounds with lower solubility showed higher leaching coefficients,which are the constants of different PAEs in Elovich equation.Considering the potential joint toxicity of PVC leachates and the importance of food security,it is recommended to use PVC products responsibly and manage plastic waste properly.
基金supported by the National Natural Science Foundation of China(No.22373084,No.62201494)Hebei Natural Science Foundation(B2022203007)the Cultivation Project for Basic Research and Innovation of Yanshan University(2024LGZD002).
文摘The adsorption properties of a magnesium porphyrin(MgP)molecule on Au(111)surface covered with up to three lay-ers of sodium chloride(NaCl)were investigated by means of first-principles calculations.The most stable adsorption configuration of MgP on the NaCl/Au(111)heterosurfaces was found to be at the Cl-top site with a 20°angle between the[110]lattice direction of NaCl and the Mg–N bond of the molecule.Compared with MgP molecule adsorbed on bare Au(111),the inclusion of NaCl lay-ers can lead to a significant decrease in the adsorption energy of the MgP molecule.The exis-tence of NaCl layers also reduced the charge transfer between the molecule and the surface.For heterosurfaces with two or three monolayers of NaCl,the charge transfer was almost com-pletely suppressed.The obtained partial density of states(PDOS)showed that hybridization between the electronic structures of the adsorbed MgP molecule and the metal surface can be significantly suppressed when NaCl layers were added.For the heterosurface with three lay-ers of NaCl,the PDOS around the Fermi level was almost identical with that of the free molecule,suggesting the electronic structure of the MgP molecule was nicely preserved.Influ-ence of the NaCl layers on the electronic structure of the MgP molecule was mainly found for molecular orbitals(MOs)away from the Fermi level as a result of the large band gap of the NaCl layers.
