BACKGROUND Hyperphosphatemia(HP)is a common complication in an advanced stage of chronic kidney disease(CKD)and is associated with cardiovascular issues,metabolic bone abnormalities and worsening of secondary hyperpar...BACKGROUND Hyperphosphatemia(HP)is a common complication in an advanced stage of chronic kidney disease(CKD)and is associated with cardiovascular issues,metabolic bone abnormalities and worsening of secondary hyperparathyroidism.Most patients on dialysis require phosphate binders to control HP.Sucroferric oxyhydroxide(SO)(Dynulta^(TM))is a calcium-free,polynuclear iron(III)based oral phosphate binder,for the treatment of HP.In this phase IV,open-label,singlearm,multi-center,12-week,SOLO CKD study evaluated efficacy and safety of Dynulta^(TM)in Indian CKD patients undergoing hemodialysis.AIM To investigate the efficacy,safety and tolerability of SO Chewable Tablet(Dynulta^(TM))in patients with CKD on hemodialysis.METHODS Hyperphosphatemic patients on hemodialysis and fulfilling eligibility criteria were included in the study for at least 12 weeks and received SO 1500 mg chewable tablet per day.The key endpoint was change in mean serum phosphorus levels after 12 weeks.Data were analysed using analysis of variance,Paired test,Wilcoxon test,and post-hoc comparisons,with P<0.05 considered statistically significant,using Graph Pad software.RESULTS A total of 114 patients were enrolled and 94 patients completed the study.The mean±SD serum phosphorous level was reduced from 7.62 mg/dL±2.02 mg/dL at baseline to 5.13 mg/dL±1.88 mg/dL after 12 weeks of treatment.At each follow-up visit,the reduction in mean serum phosphorous levels was statistically significant(P value<0.05)compared to baseline,confirming the efficacy of SO.A total of 33.33%of patients experienced adverse events(AEs).The most frequently reported AEs were pyrexia,nasopharyngitis and headache,which were considered unlikely to be related to the study drug treatment.No serious AEs was reported during the study period and no patients discontinued treatment due to AEs.CONCLUSION This first real-world study in Indian CKD patients on hemodialysis shows SO as a safe,and effective monotherapy for HP,though its small sample size limits generalizability.展开更多
The removal and recovery of low-concentration phosphates from water have become crucial due to the dual challenges of eutrophication and the phosphorus crisis.Herein,we engineered a highly efficient and recyclable pho...The removal and recovery of low-concentration phosphates from water have become crucial due to the dual challenges of eutrophication and the phosphorus crisis.Herein,we engineered a highly efficient and recyclable phosphate trapping agent of La_(2-x)CexO_(2)CO_(3) solid solution.The incorporation of Ce enhances the surface area and surface potential of La_(2-x)CexO_(2)CO_(3),providing abundant adsorption sites for phosphate.Surprisingly,we found that adjusting the Ce proportion affects the carbonate content,thereby influencing the anion-exchange capacity between carbonate and phosphate.Specifically,at 3% Ce content(3%-CeL),the carbonate ratio is maximized,resulting in an optimal sorption capacity(196.4mg P/g)and a rapid removal rate(under 40min)for phosphate,unaffected by interfering ions.Remarkably,3%-CeL achieved nearly 100%phosphate removal efficiency in diverse water samples from sewage treatment plants,rivers,reservoirs,and groundwater.After five adsorption-desorption cycles,the phosphate removal and recovery efficiency of 3%-CeL remained above 90%.Mechanistic studies revealed that 3%Ce content yielded the highest proportion of Ce^(4+)/Ce^(3+),enabling greater carbonate binding for anion-exchange.This study proposes a high-performance phosphate trapping agentwith broad applicability for treating actual waters and provides a new perspective on enhancing low-concentration phosphate removal in La-based materials through manipulating Ce ratio and valence.展开更多
In this study,a phosphate-based conversion coating(PCC)was applied as a precursor before forming silicate-fluoride(SiF)and silicate-phosphate-fluoride(SiPF)based flash-plasma electrolytic oxidation(Flash-PEO)coatings ...In this study,a phosphate-based conversion coating(PCC)was applied as a precursor before forming silicate-fluoride(SiF)and silicate-phosphate-fluoride(SiPF)based flash-plasma electrolytic oxidation(Flash-PEO)coatings on AZ31B magnesium alloy.The main novelty is the successful incorporation of calcium,zinc,manganese and phosphate species into the Flash-PEO coatings via a precursor layer rather than using the electrolyte.The precursor also led to longer lasting and more intense discharges during the PEO process,resulting in increased pore size.Corrosion studies revealed similar short-term performance for all coatings,with impedance modulus at low frequencies above 10^(7)Ωcm^(2),and slightly better performance for the SiPF-based coating.Nonetheless,the enlarged pores in the PEO coatings functionalized with the PCC precursor compromised the effectiveness of self-healing mechanisms by creating diffusion pathways for corrosive species,leading to earlier failure.These phenomena were effectively monitored by recording the open circuit potential during immersion in 0.5 wt.%NaCl solution.In summary,this study demonstrates that conversion coatings are a viable option for the functionalization of PEO coatings on magnesium alloys,as they allow for the incorporation of cationic and other species.However,it is crucial to maintain a small pore size to facilitate effective blockage through self-healing mechanisms.展开更多
The soaring demand for smart portable electronics and electric vehicles is propelling the advancements in high-energy–density lithium-ion batteries.Lithium manganese iron phosphate(LiMn_(x)Fe_(1-x)PO_(4))has garnered...The soaring demand for smart portable electronics and electric vehicles is propelling the advancements in high-energy–density lithium-ion batteries.Lithium manganese iron phosphate(LiMn_(x)Fe_(1-x)PO_(4))has garnered significant attention as a promising positive electrode material for lithium-ion batteries due to its advantages of low cost,high safety,long cycle life,high voltage,good high-temperature performance,and high energy density.Although LiMn_(x)Fe_(1-x)PO_(4)has made significant breakthroughs in the past few decades,there are still facing great challenges in poor electronic conductivity and Li-ion diffusion,manganese dissolution affecting battery cycling performance,as well as low tap density.This review systematically summarizes the reaction mechanisms,various synthesis methods,and electrochemical properties of LiMn_(x)Fe_(1-x)PO_(4)to analyze reaction processes accurately and guide material preparation.Later,the main challenges currently faced are concluded,and the corresponding various modification strategies are discussed to enhance the reaction kinetics and electrochemical performance of LiMn_(x)Fe_(1-x)PO_(4),including multi-scale particle regulation,heteroatom doping,surface coating,as well as microscopic morphology design.Finally,in view of the current research challenges faced by intrinsic reaction processes,kinetics,and energy storage applications,the promising research directions are anticipated.More importantly,it is expected to provide key insights into the development of high-performance and stable LiMn_(x)Fe_(1-x)PO_(4)materials,to achieve practical energy storage requirements.展开更多
Slow-release phosphate materials were prepared by activating insoluble phosphate with organic acid to stabilize high concentrations of Cd and Zn in contaminated smelter soil.The results showed that oxalic acid(0.1 mol...Slow-release phosphate materials were prepared by activating insoluble phosphate with organic acid to stabilize high concentrations of Cd and Zn in contaminated smelter soil.The results showed that oxalic acid(0.1 mol/L)activated tricalcium phosphate(TO-0.1)provided the most efficient stabilization of Cd and Zn.After 30 d treatment,leaching concentrations of Cd and Zn in soil were decreased from 3.17 and 16.60 mg/L to 0.078 and 0.32 mg/L,respectively.The acid-soluble fractions of Cd and Zn were transformed into reducible,oxidizable,and residual fractions.Notably,As mobility in TO-0.1 treated soils did not increase.In addition,acid rain leaching and 150 d of natural aging revealed that the slow-release phosphate material provided long-term stability for the stabilization of Cd and Zn.This study verifies the potential application of slow-release phosphate materials for the remediation of heavy metal contaminated soil at smelting sites.展开更多
The possible application of magnesium(Mg)in glaucoma surgical treatment has been investigated in our previous work.In this paper,the degradation behavior and biocompatibility of Mg coated with hydroxyapatite(HA)and di...The possible application of magnesium(Mg)in glaucoma surgical treatment has been investigated in our previous work.In this paper,the degradation behavior and biocompatibility of Mg coated with hydroxyapatite(HA)and dicalcium phosphate dihydrate(DCPD)in eye environment were evaluated,and uncoated Mg was used for comparison.It was found that uniform corrosion occurred macroscopically to the coated Mg samples in sodium lactate ringer’s injection(SLRI)as well as in the rabbit eyes.In micro-scale,the corrosion was characterized by local cracking and pitting primarily.Mg and calcium(Ca)were incorporated into the surface corrosion products and a multi-layer structure was formed.Compared to other samples,HA-coated Mg slowed down dramatically the alkalinity of the solution and the ion release of the sample,and exhibited the lowest corrosion rate in SLRI,which was about 0.22 mm/a.In terms of biocompatibility,fibroblasts demonstrated high viability in the HA-coated and DCPD-coated Mg groups(p<0.05)in vitro.In vivo,HA-coated Mg was found to show lower inflammatory response and fibrosis than the other groups did,as indicated by hematoxylin-eosin and immunofluorescence staining.During the degrading process of HA-coated Mg in the rabbits’eyes,no inflammation was found in the anterior chamber,lens,and vitreous body.HA-coated Mg was fully biodegraded fifteen weeks post-operation,and the scleral drainage channel(SDC)was formed without obvious scarring.It is concluded that HA-coated Mg implantation is a promising adjunctive procedure to improve the success rate of trabeculectomy.Statement of significance:Magnesium(Mg)has shown to be a potential biomaterial for ophthalmic implants in our previous work.However,inflammatory response resulted from the low corrosion resistance of Mg is a major concern.It is shown here that Mg coated with different calcium phosphates can improve these properties in varying degrees and keep the scleral drainage channel unobstructed and unscarred.Based on our in vitro and in vivo studies,HA-coated Mg exhibited a better degradation behavior and excellent biocompatibility.The scleral drainage channel still exists and aqueous humor flows out smoothly after the full degradation of the implant.It is concluded that HA-coated Mg is a promising biomaterial to increase the therapeutic efficiency of trabeculectomy for glaucoma.展开更多
Heterotrophic denitrification based on polylactic acid(PLAHD)can remove nitrate effectively,but it is expensive and can't remove phosphate.Autotrophic denitrification based on iron sulfide(ISAD)can simultaneously ...Heterotrophic denitrification based on polylactic acid(PLAHD)can remove nitrate effectively,but it is expensive and can't remove phosphate.Autotrophic denitrification based on iron sulfide(ISAD)can simultaneously remove nitrate and phosphate cost-effectively,but its nitrate rate is slow.So,iron sulfide mineral/polylactic acid mixotrophic biofilter(ISPLAB)was constructed to combine advantages of ISAD and PLAHD.ISPLAB achieved nitrogen and phosphorus removal rates of 98.04%and 94.12%,respectively,at a hydraulic retention time(HRT)of 24 h.The study also revealed that controlling molecular weight(MW)of PLA improved the release of soluble organic matter;adding iron sulfide enhanced the hydrolysis of PLA and precipitated PO_(4)^(3-) of Fe^(2+)/Fe^(3+),thereby facilitated simultaneous nitrogen and phosphorus removal.Microbial community analysis resulted that denitrifying bacterias(Phaeodactylibacter and Methylotenera),sulfur-reducing bacterias(Hyphomicrobium),sulfur-oxidizing bacteria(Denitratisoma),iron-reducing bacteria(Romboutsia)and hydrolyzed bacterias(norank_f_norank_o_1-20 and norank_f_Caldilineaceae)coexisted in the ISPLAB system.Organics and iron sulfide drived the denitrification process in ISPLAB.展开更多
Investigating highly effective electrocatalysts for high-temperature proton exchange membrane fuel cells(HT-PEMFC)requires the resistance to phosphate acid(PA)poisoning at cathodic oxygen reduction reaction(ORR).Recen...Investigating highly effective electrocatalysts for high-temperature proton exchange membrane fuel cells(HT-PEMFC)requires the resistance to phosphate acid(PA)poisoning at cathodic oxygen reduction reaction(ORR).Recent advancements in catalysts have focused on alleviating phosphoric anion adsorption on Pt-based catalysts with modified electronic structure or catalytic interface and developing Fe-N-C based catalysts with immunity of PA poisoning.Fe-N-C-based catalysts have emerged as promising alternatives to Pt-based catalysts,offering significant potential to overcome the characteristic adsorption of phosphate anion on Pt.An overview of these developments provides insights into catalytic mechanisms and facilitates the design of more efficient catalysts.This review begins with an exploration of basic poisoning principles,followed by a critical summary of characterization techniques employed to identified the underlying mechanism of poisoning effect.Attention is then directed to endeavors aimed at enhancing the HT-PEMFC performance by well-designed catalysts.Finally,the opportunities and challenges in developing the anti-PA poisoning strategy and practical HT-PEMFC is discussed.Through these discussions,a comprehensive understanding of PA-poisoning bottlenecks and inspire future research directions is aim to provided.展开更多
Iron phosphate based glass-ceramics with deliberately added Ce as an active nuclide simulant were prepared by microwave sintering.The sintering characteristics,including phases and structural evolution,and chemical du...Iron phosphate based glass-ceramics with deliberately added Ce as an active nuclide simulant were prepared by microwave sintering.The sintering characteristics,including phases and structural evolution,and chemical durability were investigated.XRD showed that NaZr_(2)(PO_(4))_(3) and FePO_(4) became the main crystalline phases of glass-ceramics with increasing sintering temperature.SEM revealed the glass-ceramics compactness increased first and then decreased as sintering temperature increased.Raman spectrum showed that,as sintering temperature increased,the network structure of glass-ceramics changed from mainly containing orthophosphate and pyrophosphate to a single orthophosphate.After immersion for 28 days,LR_(Na),LR_(Zr) and LR_(Ce) of the glass-ceramics prepared at 1000℃ were as low as 3.64×10^(-5),0.25×10^(-9) and 5.70×10^(-9)g/m^(2)/d respectively.The results indicate that iron phosphate based glass-ceramics can be prepared by rapid microwave sintering of glass powders and there is a potential of employing such microwave sintering technique in processing of glass-ceramics nuclear waste form.展开更多
Lithium metal batteries face serious safety challenges caused by flammable organic electrolytes and the growth of lithium dendrite.Trimethyl phosphate(TMP)is a promising alternative for flammable carbonate electrolyte...Lithium metal batteries face serious safety challenges caused by flammable organic electrolytes and the growth of lithium dendrite.Trimethyl phosphate(TMP)is a promising alternative for flammable carbonate electrolyte solvents owing to its nonflammable nature.But the low-concentration TMP-based electrolyte is unstable with the lithium metal anode.Here,a TMP-contained quasisolid electrolyte(PIQSE)with porous polyimide(PI)as supporting skeleton is designed.The cross-linking structure generated by UV curing in PIQSE can lock the reactive TMP solvent to reduce its contact with Li metal.Besides,the PI supporting skeleton with high-temperature resistance can significantly enhance the thermal stability of PIQSE.The combination of PI and TMP prompts the high ionic conductivity and excellent nonflammability of PIQSE.The LiFePO_(4)/Li cell using PIQSE shows superior electrochemical performance in a wide temperature range from-10 to 60°C.Furthermore,the cells with highvoltage cathode of LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)(NCM622)were matched with PIQSE exhibit good cyclic and rate performance.The NCM622/PIQSE/Li pouch cell was also fabricated.It exhibits a high discharge capacity of 182.9mAh.g^(-1),and can stably light up LEDs after folding and shearing tests,demonstrating broad prospects for highly safe energy storage applications.展开更多
Cresyl diphenyl phosphate(CDP),an emerging aryl organophosphate ester(OPE),exhibits potential toxic effects and is frequently found in diverse environmental media,thereby raising concerns about environmental pollution...Cresyl diphenyl phosphate(CDP),an emerging aryl organophosphate ester(OPE),exhibits potential toxic effects and is frequently found in diverse environmental media,thereby raising concerns about environmental pollution.Biodegradation demonstrates substantial potential for CDP removal from the environment.This study investigated the biodegradation mechanisms of CDP using anaerobic activated sludge(AnAS).The biodegradation of 1-mg/L CDP followed a first-order kinetic model with a degradation kinetic constant of 0.943 d^(-1),and the addition of different electron acceptors affected the degradation rate.High-resolution mass spectrometry identified seven transformation products(TPs)of CDP.The pathways of CDP degradation in anaerobic conditions were proposed,with carboxylation products being the most dominant intermediate products.The structure of the anaerobic microbial community at different degradation time points in CDP-amended microcosms was examined.The linear discriminant analysis(LDA)of effect size(LEfSe)potentially underscored the pivotal role of Methyloversatilis in CDP biodegradation.Zebrafish embryotoxicity experiments revealed both lethal and morphogenetic impacts of CDP on zebrafish embryos.The survival rate,hatching rate,and body length indicators of zebrafish embryos underscored the detoxification of CDP and its resultant intermediates by AnAS.This study offers new insights into the fate and biodegradation mechanisms of CDP in wastewater treatment plants.展开更多
The authors regret that due to negligence,the picture was misplaced in the original manuscript,resulting in Fig.6d being incorrectly included.The correct version of Fig.6d is provided below for reference.This error do...The authors regret that due to negligence,the picture was misplaced in the original manuscript,resulting in Fig.6d being incorrectly included.The correct version of Fig.6d is provided below for reference.This error does not affect the conclusions of the study,and we apologize for any confusion it may have caused.展开更多
The interaction mechanism between eggshell calcium and endogenous silica in biomass during biochar modification,and its impact on phosphate adsorption performance and slow-release fertilizer characteristics,remains un...The interaction mechanism between eggshell calcium and endogenous silica in biomass during biochar modification,and its impact on phosphate adsorption performance and slow-release fertilizer characteristics,remains unexplored.This study investigates that high silica content in biomass(>6%)inhibits the decomposition of CaCO_(3)in eggshells during pyrolysis,reducing the formation of active calcium species(CaO and Ca(OH)_(2)),while moderate silica levels(4%-5%)promote the formation of CaSiO_(3),enhancing phosphorus adsorption without hindering Ca^(2+)activation.Adsorption studies reveal that the precipitation of Ca_(5)(PO_(4))_(3)(OH)resulting from the combination of CaO and Ca(OH)_(2)with phosphate is the primary and effective form for phosphorus removal in calcium-modified adsorbents,accompanied by Ca_(3)(PO_(4))_(2)·2H_(2)O precipitation formed by CaSi O_(3).Eggshell calcium-modified corn straw biochar(ECS)exhibited the highest adsorption capacity,reaching 123.3 mg/g,outperforming materials in previous studies.ECS also demonstrated excellent pH adaptability and selective phosphate removal.As a biochar-based phosphorus fertilizer,ECS-P exhibits high phosphorus extractability in formic acid(93.92%)but low water solubility(0.62%),with phosphorus release during the seven-day intermittent leaching experiment remaining between 0.53 to 0.875 mg/L.These results confirm its potential as a phosphorus cycling fertilizer.This study provides fundamental insights into optimizing biomass selection based on silica content for calcium modification,offering an efficient strategy for both phosphate recovery and slow-release fertilizer development.展开更多
The efficient recycling of spent lithium iron phosphate(LiFePO_(4),also referred to as LFP)should convert Fe(Ⅱ)to Fe(Ⅲ),which is key to the extraction of Li and separation of Fe and is not well understood.Herein,we ...The efficient recycling of spent lithium iron phosphate(LiFePO_(4),also referred to as LFP)should convert Fe(Ⅱ)to Fe(Ⅲ),which is key to the extraction of Li and separation of Fe and is not well understood.Herein,we systematically study the oxidation of LiFePO_(4)in the air and in the solution containing oxidants such as H_(2)O_(2)and the effect of oxidation on the leaching behaviors of LFP.In the air,O_(2)breaks down the LFP olivine structure at 550℃for 1 h by oxidizing Fe(Ⅱ)to Fe(Ⅲ)in terms of converting LFP to Li_(3)Fe_(2)(PO_(4))_(3)and Fe_(2)O_(3).After that,Li is leached in 0.5 M sulfuric acid solution and is further recycled as Li_(3)PO_(4)with a Li recovery efficiency of 97.48%.Meanwhile,Fe is recovered as FePO_(4)and Fe_(2)O_(3).Compared with H_(2)SO_(4)-H_(2)O_(2),the air oxidation saves H_(2)O_(2)but increases the leaching efficiency of Fe and H_(2)SO_(4)consumption.The discrepancy of Fe leaching efficiency can be attributed to the different leaching mechanisms involving the solid-to-solid and solid-to-liquid-to-solid conversions.Furthermore,the results of the Everbatt model analysis show that the air roasting-H_(2)SO_(4)leaching method has low emission and potentially high income,which is simple and safe.Overall,this work will deepen the understanding of acid leaching of LFP and favorably stimulate the maturation of the LFP recycling technique.展开更多
The adsorption of phosphate was conducted by the complex of chitosan/polyacrylamide/ferric(CS/PAM/Fe(Ⅲ))prepared.The SEM images and XPS spectra confirmed the successful adsorption of phosphate.The adsorption process ...The adsorption of phosphate was conducted by the complex of chitosan/polyacrylamide/ferric(CS/PAM/Fe(Ⅲ))prepared.The SEM images and XPS spectra confirmed the successful adsorption of phosphate.The adsorption process was studied by varying the influencing aspects like pH,co-existing ions,contact time,and initial phosphate concentration.The experimental results indicate that the adsorptive capacity decreases with the increase of pH.However,it is commendable that there is still a adsorption capacity of more than 5 mg/g when the pH is 8-11.The adsorption kinetics can be accurately described by the pseudo-second-order model and is controlled by both chemisorption and surface diffusion.The adsorption process is a single layer adsorption.This paper proposed that the adsorption mechanism of CS/PAM/Fe(Ⅲ)complex is the joint action of electrostatic attraction and ligand exchange.展开更多
Lithium iron phosphate(LFP)has found many applications in the field of electric vehicles and energy storage systems.However,the increasing volume of end-of-life LFP batteries poses an urgent challenge in terms of envi...Lithium iron phosphate(LFP)has found many applications in the field of electric vehicles and energy storage systems.However,the increasing volume of end-of-life LFP batteries poses an urgent challenge in terms of environmental sustainability and resource management.Therefore,the development and implementation of efficient LFP battery recycling methods are crucial to address these challenges.This article presents a novel,comprehensive evaluation framework for comparing different lithium iron phosphate relithiation techniques.The framework includes three main sets of criteria:direct production cost,electrochemical performance,and environmental impact.Each criterion is scored on a scale of 0–100,with higher scores indicating better performance.The direct production cost is rated based on material costs,energy consumption,key equipment costs,process duration and space requirements.Electrochemical performance is assessed by rate capability and cycle stability.Environmental impact is assessed based on CO_(2)emissions.The framework provides a standardized technique for researchers and industry professionals to objectively compare relithiation methods,facilitating the identification of the most promising approaches for further development and scale-up.The total average score across the three criterion groups for electrochemical,chemical,and hydrothermal relithiation methods was approximately 60 points,while sintering scored 39 points,making it the least attractive relithiation technique.Combining approaches outlined in publications with scores exceeding 60,a relithiation scheme was proposed to achieve optimal electrochemical performance with minimal resource consumption and environmental impact.The results demonstrate the framework’s applicability and highlight areas for future research and optimization in lithium iron phosphate cathode recycling.展开更多
Oseltamivir phosphate(OP),renowned as one of the most effective drugs for influenza treatment,encounters several challenges,including poor stability,difficulty in swallowing,and a bitter taste,thereby limiting its com...Oseltamivir phosphate(OP),renowned as one of the most effective drugs for influenza treatment,encounters several challenges,including poor stability,difficulty in swallowing,and a bitter taste,thereby limiting its compliance,particularly among children.Consequently,this study aimed to devise a novel sustained-release suspension of OP employing an ion exchange resin as a carrier to address these challenges.The OP-drug resin complex(OP-DRC)was synthesized utilizing ion exchange technology,while OP-coated microcapsules(OP-CM)were fabricated via the emulsion-evaporation method.The optimization of the formulation process for the OP sustained-release suspension was achieved through a combination of single-factor experimentation and orthogonal experimental design.Furthermore,the drug release kinetics and pharmacokinetic properties of the sustained-release suspension were thoroughly evaluated both in vitro and in vivo.Scanning electron microscopy(SEM),X-ray diffraction(XRD),and attenuated total reflectance Fourier-transform infrared spectroscopy(ATR-FTIR)analyses confirmed the formation of drug-resin complexes via ionic bonding.The in vitro cumulative release rates were found to be 16%(1 h),53%(6 h),and 84%(24 h),respectively.Notably,the self-made sustained-release suspension exhibited an extended half-life(21.518 h),delayed time to peak concentration(T_(max))(6 h),and reduced maximum plasma concentration(C_(max))(0.397μg/mL)in comparison to commercial granules(half-life=8.466 h;T_(max)=2 h;C_(max)=0.631μg/mL).Additionally,the area under the curve(AUC)indicated that the bioavailability of the self-made OP suspension surpassed that of the commercial OP granules by 101%.These findings underscored the successful development of an oral OP sustained-release suspension characterized by stability,tastelessness,ease of swallowing,convenient administration,and sustained-release properties,thereby potentially enhancing drug compliance among children.展开更多
In order to obtain a more protective phosphate conversion coating with a denser architecture,the nucleation kinetics of phosphate chemical conversion coating on Mg-Gd-Y-Zr magnesium alloy was tuned in this work.A pret...In order to obtain a more protective phosphate conversion coating with a denser architecture,the nucleation kinetics of phosphate chemical conversion coating on Mg-Gd-Y-Zr magnesium alloy was tuned in this work.A pretreatment process was proposed and organic additives were incorporated,which aims at increasing the ionic produce(J_(sp))at the interface for increasingσ,and decreasing the critical ionic product(J_(C,sp)),respectively.Results prove that the pretreatment of bare alloys in a phosphate bath could increase the ion products of MgHPO_(4)/MnHPO_(4).The addition of benzalkonium chloride could neutralize the charges of crystals,and in turn promote the nucleation kinetics.A denser and more protective conversion coating could consequently be obtained.展开更多
Inorganic phosphate(Pi)homeostasis in plants is regulated by inositol pyrophosphates(PP-InsPs),which mediate phosphate starvation responses.While beneficial microorganisms,such as arbuscular mycorrhizal fungi,contribu...Inorganic phosphate(Pi)homeostasis in plants is regulated by inositol pyrophosphates(PP-InsPs),which mediate phosphate starvation responses.While beneficial microorganisms,such as arbuscular mycorrhizal fungi,contribute to phosphate uptake,pathogenic fungi often exploit phosphate metabolism to enhance virulence.However,the exact mechanisms by which pathogens manipulate plant phosphate signaling remain largely unknown.Here,we highlight a recent study by Ulrich Schaffrath and colleagues(Science,2025)revealing that plant pathogenic fungi deploy conserved Nudix hydrolase effectors to hydrolyze PP-InsPs,thereby mimicking phosphate starvation and suppressing host immunity.These findings not only expand our understanding of plantpathogen interactions,but also open new avenues for crop protection and resistance breeding.展开更多
Objective Nicotinamide adenine dinucleotide phosphate(NADPH)oxidases(NOXs)are known as major sources of reactive oxygen species(ROS),yet their role in regulating cellular antioxidative metabolism and ferroptosis is un...Objective Nicotinamide adenine dinucleotide phosphate(NADPH)oxidases(NOXs)are known as major sources of reactive oxygen species(ROS),yet their role in regulating cellular antioxidative metabolism and ferroptosis is unclear.This study assessed the expression and clinical relevance of NOXs across pan-cancer and investigated the role of NOX4 in colorectal cancer progression Methods We analyzed transcriptomic and survival data from The Cancer Genome Atlas(TCGA)for NOXs across 22 types of solid tumors.A CRISPR library targeting NOXs was developed for potential therapeutic target screening in colorectal cancer cells(CRCs).Techniques such as CRISPR-knockout cell lines,1,2-13C-glucose tracing,PI staining,BrdU assays,and coimmunoprecipitation were employed to elucidate the function of NOX4 in CRCs.Results NOX4 emerged as a key therapeutic target for colorectal cancer from TCGA data.CRISPR screening highlighted its essential role in CRC survival,with functional experiments confirming that NOX4 upregulation promotes cell survival and proliferation.The interaction of NOX4 with glucose‑6‑phosphate dehydrogenase(G6PD)was found to enhance the pentose phosphate pathway(PPP),facilitating ROS clearance and protecting CRCs against ferroptosis.Conclusions This study identified NOX4 as a novel ferroptosis suppressor and a therapeutic target for the treatment of colorectal cancer.The findings suggest that a coupling between NADPH oxidase enzyme NOX4 and the PPP regulates ferroptosis and reveal an accompanying metabolic vulnerability for therapeutic targeting in colorectal cancer.展开更多
文摘BACKGROUND Hyperphosphatemia(HP)is a common complication in an advanced stage of chronic kidney disease(CKD)and is associated with cardiovascular issues,metabolic bone abnormalities and worsening of secondary hyperparathyroidism.Most patients on dialysis require phosphate binders to control HP.Sucroferric oxyhydroxide(SO)(Dynulta^(TM))is a calcium-free,polynuclear iron(III)based oral phosphate binder,for the treatment of HP.In this phase IV,open-label,singlearm,multi-center,12-week,SOLO CKD study evaluated efficacy and safety of Dynulta^(TM)in Indian CKD patients undergoing hemodialysis.AIM To investigate the efficacy,safety and tolerability of SO Chewable Tablet(Dynulta^(TM))in patients with CKD on hemodialysis.METHODS Hyperphosphatemic patients on hemodialysis and fulfilling eligibility criteria were included in the study for at least 12 weeks and received SO 1500 mg chewable tablet per day.The key endpoint was change in mean serum phosphorus levels after 12 weeks.Data were analysed using analysis of variance,Paired test,Wilcoxon test,and post-hoc comparisons,with P<0.05 considered statistically significant,using Graph Pad software.RESULTS A total of 114 patients were enrolled and 94 patients completed the study.The mean±SD serum phosphorous level was reduced from 7.62 mg/dL±2.02 mg/dL at baseline to 5.13 mg/dL±1.88 mg/dL after 12 weeks of treatment.At each follow-up visit,the reduction in mean serum phosphorous levels was statistically significant(P value<0.05)compared to baseline,confirming the efficacy of SO.A total of 33.33%of patients experienced adverse events(AEs).The most frequently reported AEs were pyrexia,nasopharyngitis and headache,which were considered unlikely to be related to the study drug treatment.No serious AEs was reported during the study period and no patients discontinued treatment due to AEs.CONCLUSION This first real-world study in Indian CKD patients on hemodialysis shows SO as a safe,and effective monotherapy for HP,though its small sample size limits generalizability.
基金supported by the National Key Research and Development Program of China(Nos.2022YFC3703700,2021YFA0910300,and 2021YFC3200902)the National Natural Science Foundation of China(No.22125606)+1 种基金the Special Project of Ecological Environmental Technology for Carbon Dioxide Emissions Peak and Carbon Neutrality(No.RCEESTDZ-2021-21)China South-to-North Water Diversion Corporation Limited Research Project(No.NSBDZX/SH/KY/2022-001).
文摘The removal and recovery of low-concentration phosphates from water have become crucial due to the dual challenges of eutrophication and the phosphorus crisis.Herein,we engineered a highly efficient and recyclable phosphate trapping agent of La_(2-x)CexO_(2)CO_(3) solid solution.The incorporation of Ce enhances the surface area and surface potential of La_(2-x)CexO_(2)CO_(3),providing abundant adsorption sites for phosphate.Surprisingly,we found that adjusting the Ce proportion affects the carbonate content,thereby influencing the anion-exchange capacity between carbonate and phosphate.Specifically,at 3% Ce content(3%-CeL),the carbonate ratio is maximized,resulting in an optimal sorption capacity(196.4mg P/g)and a rapid removal rate(under 40min)for phosphate,unaffected by interfering ions.Remarkably,3%-CeL achieved nearly 100%phosphate removal efficiency in diverse water samples from sewage treatment plants,rivers,reservoirs,and groundwater.After five adsorption-desorption cycles,the phosphate removal and recovery efficiency of 3%-CeL remained above 90%.Mechanistic studies revealed that 3%Ce content yielded the highest proportion of Ce^(4+)/Ce^(3+),enabling greater carbonate binding for anion-exchange.This study proposes a high-performance phosphate trapping agentwith broad applicability for treating actual waters and provides a new perspective on enhancing low-concentration phosphate removal in La-based materials through manipulating Ce ratio and valence.
基金support of the PID2021-124341OB-C22/AEI/10.13039/501100011033/FEDER,UE(MICIU)J.M.Vega also acknowledges the Grant RYC2021-034384-I funded by MICIU/AEI/10.13039/501100011033 and by“European Union Next Generation EU/PRTR”.
文摘In this study,a phosphate-based conversion coating(PCC)was applied as a precursor before forming silicate-fluoride(SiF)and silicate-phosphate-fluoride(SiPF)based flash-plasma electrolytic oxidation(Flash-PEO)coatings on AZ31B magnesium alloy.The main novelty is the successful incorporation of calcium,zinc,manganese and phosphate species into the Flash-PEO coatings via a precursor layer rather than using the electrolyte.The precursor also led to longer lasting and more intense discharges during the PEO process,resulting in increased pore size.Corrosion studies revealed similar short-term performance for all coatings,with impedance modulus at low frequencies above 10^(7)Ωcm^(2),and slightly better performance for the SiPF-based coating.Nonetheless,the enlarged pores in the PEO coatings functionalized with the PCC precursor compromised the effectiveness of self-healing mechanisms by creating diffusion pathways for corrosive species,leading to earlier failure.These phenomena were effectively monitored by recording the open circuit potential during immersion in 0.5 wt.%NaCl solution.In summary,this study demonstrates that conversion coatings are a viable option for the functionalization of PEO coatings on magnesium alloys,as they allow for the incorporation of cationic and other species.However,it is crucial to maintain a small pore size to facilitate effective blockage through self-healing mechanisms.
基金National Natural Science Foundation of China(52104294)Fundamental Research Funds for the Central Universities(FRF-TP-19-079A1)。
文摘The soaring demand for smart portable electronics and electric vehicles is propelling the advancements in high-energy–density lithium-ion batteries.Lithium manganese iron phosphate(LiMn_(x)Fe_(1-x)PO_(4))has garnered significant attention as a promising positive electrode material for lithium-ion batteries due to its advantages of low cost,high safety,long cycle life,high voltage,good high-temperature performance,and high energy density.Although LiMn_(x)Fe_(1-x)PO_(4)has made significant breakthroughs in the past few decades,there are still facing great challenges in poor electronic conductivity and Li-ion diffusion,manganese dissolution affecting battery cycling performance,as well as low tap density.This review systematically summarizes the reaction mechanisms,various synthesis methods,and electrochemical properties of LiMn_(x)Fe_(1-x)PO_(4)to analyze reaction processes accurately and guide material preparation.Later,the main challenges currently faced are concluded,and the corresponding various modification strategies are discussed to enhance the reaction kinetics and electrochemical performance of LiMn_(x)Fe_(1-x)PO_(4),including multi-scale particle regulation,heteroatom doping,surface coating,as well as microscopic morphology design.Finally,in view of the current research challenges faced by intrinsic reaction processes,kinetics,and energy storage applications,the promising research directions are anticipated.More importantly,it is expected to provide key insights into the development of high-performance and stable LiMn_(x)Fe_(1-x)PO_(4)materials,to achieve practical energy storage requirements.
基金supported by the Natural Science Foundation of Hunan Province,China(No.2024JJ1012)the Postgraduate Innovative Project of Central South University,China(No.2023ZZTS0459)the National Key Research and Development Program of China(No.2019YFC1803605)。
文摘Slow-release phosphate materials were prepared by activating insoluble phosphate with organic acid to stabilize high concentrations of Cd and Zn in contaminated smelter soil.The results showed that oxalic acid(0.1 mol/L)activated tricalcium phosphate(TO-0.1)provided the most efficient stabilization of Cd and Zn.After 30 d treatment,leaching concentrations of Cd and Zn in soil were decreased from 3.17 and 16.60 mg/L to 0.078 and 0.32 mg/L,respectively.The acid-soluble fractions of Cd and Zn were transformed into reducible,oxidizable,and residual fractions.Notably,As mobility in TO-0.1 treated soils did not increase.In addition,acid rain leaching and 150 d of natural aging revealed that the slow-release phosphate material provided long-term stability for the stabilization of Cd and Zn.This study verifies the potential application of slow-release phosphate materials for the remediation of heavy metal contaminated soil at smelting sites.
基金supported by the Natural Science Foundation of Chongqing(Grant No.csts2018jcyjAX0016)Funded by the Senior Medical Talents Program of Chongqing for Young and Middle-aged.
文摘The possible application of magnesium(Mg)in glaucoma surgical treatment has been investigated in our previous work.In this paper,the degradation behavior and biocompatibility of Mg coated with hydroxyapatite(HA)and dicalcium phosphate dihydrate(DCPD)in eye environment were evaluated,and uncoated Mg was used for comparison.It was found that uniform corrosion occurred macroscopically to the coated Mg samples in sodium lactate ringer’s injection(SLRI)as well as in the rabbit eyes.In micro-scale,the corrosion was characterized by local cracking and pitting primarily.Mg and calcium(Ca)were incorporated into the surface corrosion products and a multi-layer structure was formed.Compared to other samples,HA-coated Mg slowed down dramatically the alkalinity of the solution and the ion release of the sample,and exhibited the lowest corrosion rate in SLRI,which was about 0.22 mm/a.In terms of biocompatibility,fibroblasts demonstrated high viability in the HA-coated and DCPD-coated Mg groups(p<0.05)in vitro.In vivo,HA-coated Mg was found to show lower inflammatory response and fibrosis than the other groups did,as indicated by hematoxylin-eosin and immunofluorescence staining.During the degrading process of HA-coated Mg in the rabbits’eyes,no inflammation was found in the anterior chamber,lens,and vitreous body.HA-coated Mg was fully biodegraded fifteen weeks post-operation,and the scleral drainage channel(SDC)was formed without obvious scarring.It is concluded that HA-coated Mg implantation is a promising adjunctive procedure to improve the success rate of trabeculectomy.Statement of significance:Magnesium(Mg)has shown to be a potential biomaterial for ophthalmic implants in our previous work.However,inflammatory response resulted from the low corrosion resistance of Mg is a major concern.It is shown here that Mg coated with different calcium phosphates can improve these properties in varying degrees and keep the scleral drainage channel unobstructed and unscarred.Based on our in vitro and in vivo studies,HA-coated Mg exhibited a better degradation behavior and excellent biocompatibility.The scleral drainage channel still exists and aqueous humor flows out smoothly after the full degradation of the implant.It is concluded that HA-coated Mg is a promising biomaterial to increase the therapeutic efficiency of trabeculectomy for glaucoma.
基金supported by the National Key Research and Development Program of China(No.2021YFC3201505-02)Shenzhen Science and Technology Plan Collaborative Innovation Project-Undertake Major National Science and Technology Projects of China(No.CJGJZD2020061710260200).
文摘Heterotrophic denitrification based on polylactic acid(PLAHD)can remove nitrate effectively,but it is expensive and can't remove phosphate.Autotrophic denitrification based on iron sulfide(ISAD)can simultaneously remove nitrate and phosphate cost-effectively,but its nitrate rate is slow.So,iron sulfide mineral/polylactic acid mixotrophic biofilter(ISPLAB)was constructed to combine advantages of ISAD and PLAHD.ISPLAB achieved nitrogen and phosphorus removal rates of 98.04%and 94.12%,respectively,at a hydraulic retention time(HRT)of 24 h.The study also revealed that controlling molecular weight(MW)of PLA improved the release of soluble organic matter;adding iron sulfide enhanced the hydrolysis of PLA and precipitated PO_(4)^(3-) of Fe^(2+)/Fe^(3+),thereby facilitated simultaneous nitrogen and phosphorus removal.Microbial community analysis resulted that denitrifying bacterias(Phaeodactylibacter and Methylotenera),sulfur-reducing bacterias(Hyphomicrobium),sulfur-oxidizing bacteria(Denitratisoma),iron-reducing bacteria(Romboutsia)and hydrolyzed bacterias(norank_f_norank_o_1-20 and norank_f_Caldilineaceae)coexisted in the ISPLAB system.Organics and iron sulfide drived the denitrification process in ISPLAB.
文摘Investigating highly effective electrocatalysts for high-temperature proton exchange membrane fuel cells(HT-PEMFC)requires the resistance to phosphate acid(PA)poisoning at cathodic oxygen reduction reaction(ORR).Recent advancements in catalysts have focused on alleviating phosphoric anion adsorption on Pt-based catalysts with modified electronic structure or catalytic interface and developing Fe-N-C based catalysts with immunity of PA poisoning.Fe-N-C-based catalysts have emerged as promising alternatives to Pt-based catalysts,offering significant potential to overcome the characteristic adsorption of phosphate anion on Pt.An overview of these developments provides insights into catalytic mechanisms and facilitates the design of more efficient catalysts.This review begins with an exploration of basic poisoning principles,followed by a critical summary of characterization techniques employed to identified the underlying mechanism of poisoning effect.Attention is then directed to endeavors aimed at enhancing the HT-PEMFC performance by well-designed catalysts.Finally,the opportunities and challenges in developing the anti-PA poisoning strategy and practical HT-PEMFC is discussed.Through these discussions,a comprehensive understanding of PA-poisoning bottlenecks and inspire future research directions is aim to provided.
基金Funded by the Key Research and Development Projects of Anhui Province(No.2022a05020026)the Key Technologies R&D Program of CNBM(Nos.2021HX0809,2021HX1011)the Anhui Science and Technology Major Project(No.2021e03020009)。
文摘Iron phosphate based glass-ceramics with deliberately added Ce as an active nuclide simulant were prepared by microwave sintering.The sintering characteristics,including phases and structural evolution,and chemical durability were investigated.XRD showed that NaZr_(2)(PO_(4))_(3) and FePO_(4) became the main crystalline phases of glass-ceramics with increasing sintering temperature.SEM revealed the glass-ceramics compactness increased first and then decreased as sintering temperature increased.Raman spectrum showed that,as sintering temperature increased,the network structure of glass-ceramics changed from mainly containing orthophosphate and pyrophosphate to a single orthophosphate.After immersion for 28 days,LR_(Na),LR_(Zr) and LR_(Ce) of the glass-ceramics prepared at 1000℃ were as low as 3.64×10^(-5),0.25×10^(-9) and 5.70×10^(-9)g/m^(2)/d respectively.The results indicate that iron phosphate based glass-ceramics can be prepared by rapid microwave sintering of glass powders and there is a potential of employing such microwave sintering technique in processing of glass-ceramics nuclear waste form.
基金financially supported by the Natural Science Basic Research Program of Shaanxi Province(No.2024JC-YBQN-0582)the Natural Science Foundation of Shaanxi Provincial Department of Education(No.23JK0702)+1 种基金Scientific Research fund of Xijing University(No.XJ23B05)the Fundamental Research Funds for the Central Universities(No.xzy012024005)。
文摘Lithium metal batteries face serious safety challenges caused by flammable organic electrolytes and the growth of lithium dendrite.Trimethyl phosphate(TMP)is a promising alternative for flammable carbonate electrolyte solvents owing to its nonflammable nature.But the low-concentration TMP-based electrolyte is unstable with the lithium metal anode.Here,a TMP-contained quasisolid electrolyte(PIQSE)with porous polyimide(PI)as supporting skeleton is designed.The cross-linking structure generated by UV curing in PIQSE can lock the reactive TMP solvent to reduce its contact with Li metal.Besides,the PI supporting skeleton with high-temperature resistance can significantly enhance the thermal stability of PIQSE.The combination of PI and TMP prompts the high ionic conductivity and excellent nonflammability of PIQSE.The LiFePO_(4)/Li cell using PIQSE shows superior electrochemical performance in a wide temperature range from-10 to 60°C.Furthermore,the cells with highvoltage cathode of LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)(NCM622)were matched with PIQSE exhibit good cyclic and rate performance.The NCM622/PIQSE/Li pouch cell was also fabricated.It exhibits a high discharge capacity of 182.9mAh.g^(-1),and can stably light up LEDs after folding and shearing tests,demonstrating broad prospects for highly safe energy storage applications.
基金supported by the National Natural Science Foundation of China(Grants No.52270155 and 92047201).
文摘Cresyl diphenyl phosphate(CDP),an emerging aryl organophosphate ester(OPE),exhibits potential toxic effects and is frequently found in diverse environmental media,thereby raising concerns about environmental pollution.Biodegradation demonstrates substantial potential for CDP removal from the environment.This study investigated the biodegradation mechanisms of CDP using anaerobic activated sludge(AnAS).The biodegradation of 1-mg/L CDP followed a first-order kinetic model with a degradation kinetic constant of 0.943 d^(-1),and the addition of different electron acceptors affected the degradation rate.High-resolution mass spectrometry identified seven transformation products(TPs)of CDP.The pathways of CDP degradation in anaerobic conditions were proposed,with carboxylation products being the most dominant intermediate products.The structure of the anaerobic microbial community at different degradation time points in CDP-amended microcosms was examined.The linear discriminant analysis(LDA)of effect size(LEfSe)potentially underscored the pivotal role of Methyloversatilis in CDP biodegradation.Zebrafish embryotoxicity experiments revealed both lethal and morphogenetic impacts of CDP on zebrafish embryos.The survival rate,hatching rate,and body length indicators of zebrafish embryos underscored the detoxification of CDP and its resultant intermediates by AnAS.This study offers new insights into the fate and biodegradation mechanisms of CDP in wastewater treatment plants.
文摘The authors regret that due to negligence,the picture was misplaced in the original manuscript,resulting in Fig.6d being incorrectly included.The correct version of Fig.6d is provided below for reference.This error does not affect the conclusions of the study,and we apologize for any confusion it may have caused.
基金supported by Hebei Key Laboratory of Mineral Resources and Ecological Environment Monitoring(No.HBMREEM202302)Tianjin Key Research and Development Science and Technology Project(Nos.24YFXTHZ00170 and 24YFXTHZ00050)。
文摘The interaction mechanism between eggshell calcium and endogenous silica in biomass during biochar modification,and its impact on phosphate adsorption performance and slow-release fertilizer characteristics,remains unexplored.This study investigates that high silica content in biomass(>6%)inhibits the decomposition of CaCO_(3)in eggshells during pyrolysis,reducing the formation of active calcium species(CaO and Ca(OH)_(2)),while moderate silica levels(4%-5%)promote the formation of CaSiO_(3),enhancing phosphorus adsorption without hindering Ca^(2+)activation.Adsorption studies reveal that the precipitation of Ca_(5)(PO_(4))_(3)(OH)resulting from the combination of CaO and Ca(OH)_(2)with phosphate is the primary and effective form for phosphorus removal in calcium-modified adsorbents,accompanied by Ca_(3)(PO_(4))_(2)·2H_(2)O precipitation formed by CaSi O_(3).Eggshell calcium-modified corn straw biochar(ECS)exhibited the highest adsorption capacity,reaching 123.3 mg/g,outperforming materials in previous studies.ECS also demonstrated excellent pH adaptability and selective phosphate removal.As a biochar-based phosphorus fertilizer,ECS-P exhibits high phosphorus extractability in formic acid(93.92%)but low water solubility(0.62%),with phosphorus release during the seven-day intermittent leaching experiment remaining between 0.53 to 0.875 mg/L.These results confirm its potential as a phosphorus cycling fertilizer.This study provides fundamental insights into optimizing biomass selection based on silica content for calcium modification,offering an efficient strategy for both phosphate recovery and slow-release fertilizer development.
基金supported by the Chilwee Group(No.CWDY-ZH-YJY-202101-001)the Fundamental Research Funds for the Central Universities(No.2042023kf0214)the Starting Funding from Wuhan University.
文摘The efficient recycling of spent lithium iron phosphate(LiFePO_(4),also referred to as LFP)should convert Fe(Ⅱ)to Fe(Ⅲ),which is key to the extraction of Li and separation of Fe and is not well understood.Herein,we systematically study the oxidation of LiFePO_(4)in the air and in the solution containing oxidants such as H_(2)O_(2)and the effect of oxidation on the leaching behaviors of LFP.In the air,O_(2)breaks down the LFP olivine structure at 550℃for 1 h by oxidizing Fe(Ⅱ)to Fe(Ⅲ)in terms of converting LFP to Li_(3)Fe_(2)(PO_(4))_(3)and Fe_(2)O_(3).After that,Li is leached in 0.5 M sulfuric acid solution and is further recycled as Li_(3)PO_(4)with a Li recovery efficiency of 97.48%.Meanwhile,Fe is recovered as FePO_(4)and Fe_(2)O_(3).Compared with H_(2)SO_(4)-H_(2)O_(2),the air oxidation saves H_(2)O_(2)but increases the leaching efficiency of Fe and H_(2)SO_(4)consumption.The discrepancy of Fe leaching efficiency can be attributed to the different leaching mechanisms involving the solid-to-solid and solid-to-liquid-to-solid conversions.Furthermore,the results of the Everbatt model analysis show that the air roasting-H_(2)SO_(4)leaching method has low emission and potentially high income,which is simple and safe.Overall,this work will deepen the understanding of acid leaching of LFP and favorably stimulate the maturation of the LFP recycling technique.
基金Funded by the Provincial Natural Science Foundation for Universities of AnhuiChina(No.KJ2021A0624)+1 种基金the Director's Fund of Anhui Province Advanced Building Materials International Research Center(No.JZCL2207ZR)the Anhui Jianzhu University Talent Introduction and Doctoral Start-up Fund(No.2023QDZ23)。
文摘The adsorption of phosphate was conducted by the complex of chitosan/polyacrylamide/ferric(CS/PAM/Fe(Ⅲ))prepared.The SEM images and XPS spectra confirmed the successful adsorption of phosphate.The adsorption process was studied by varying the influencing aspects like pH,co-existing ions,contact time,and initial phosphate concentration.The experimental results indicate that the adsorptive capacity decreases with the increase of pH.However,it is commendable that there is still a adsorption capacity of more than 5 mg/g when the pH is 8-11.The adsorption kinetics can be accurately described by the pseudo-second-order model and is controlled by both chemisorption and surface diffusion.The adsorption process is a single layer adsorption.This paper proposed that the adsorption mechanism of CS/PAM/Fe(Ⅲ)complex is the joint action of electrostatic attraction and ligand exchange.
基金state assignments of Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry,Russian Academy of Sciences(No.124013000692-4 and 122112100037-4).
文摘Lithium iron phosphate(LFP)has found many applications in the field of electric vehicles and energy storage systems.However,the increasing volume of end-of-life LFP batteries poses an urgent challenge in terms of environmental sustainability and resource management.Therefore,the development and implementation of efficient LFP battery recycling methods are crucial to address these challenges.This article presents a novel,comprehensive evaluation framework for comparing different lithium iron phosphate relithiation techniques.The framework includes three main sets of criteria:direct production cost,electrochemical performance,and environmental impact.Each criterion is scored on a scale of 0–100,with higher scores indicating better performance.The direct production cost is rated based on material costs,energy consumption,key equipment costs,process duration and space requirements.Electrochemical performance is assessed by rate capability and cycle stability.Environmental impact is assessed based on CO_(2)emissions.The framework provides a standardized technique for researchers and industry professionals to objectively compare relithiation methods,facilitating the identification of the most promising approaches for further development and scale-up.The total average score across the three criterion groups for electrochemical,chemical,and hydrothermal relithiation methods was approximately 60 points,while sintering scored 39 points,making it the least attractive relithiation technique.Combining approaches outlined in publications with scores exceeding 60,a relithiation scheme was proposed to achieve optimal electrochemical performance with minimal resource consumption and environmental impact.The results demonstrate the framework’s applicability and highlight areas for future research and optimization in lithium iron phosphate cathode recycling.
基金2023 Nantong Jianghai Talents Project2023 Nantong Social Livelihood Science and Technology Plan+4 种基金2021 Jurong Social Development Science&Technology Program(Grant No.ZA42109)2022 New Drugs and Platform Enhancement Project of the Yangtze Delta Drug Advanced Research InstituteChina Postdoctoral Science Foundation(Grant No.2020M681532)Jiangsu Planned Projects for Postdoctoral Research Funds(Grant No.2020Z209)Natural Science Research Projects of Universities in Jiangsu Province(Grant No.20KJD350001)。
文摘Oseltamivir phosphate(OP),renowned as one of the most effective drugs for influenza treatment,encounters several challenges,including poor stability,difficulty in swallowing,and a bitter taste,thereby limiting its compliance,particularly among children.Consequently,this study aimed to devise a novel sustained-release suspension of OP employing an ion exchange resin as a carrier to address these challenges.The OP-drug resin complex(OP-DRC)was synthesized utilizing ion exchange technology,while OP-coated microcapsules(OP-CM)were fabricated via the emulsion-evaporation method.The optimization of the formulation process for the OP sustained-release suspension was achieved through a combination of single-factor experimentation and orthogonal experimental design.Furthermore,the drug release kinetics and pharmacokinetic properties of the sustained-release suspension were thoroughly evaluated both in vitro and in vivo.Scanning electron microscopy(SEM),X-ray diffraction(XRD),and attenuated total reflectance Fourier-transform infrared spectroscopy(ATR-FTIR)analyses confirmed the formation of drug-resin complexes via ionic bonding.The in vitro cumulative release rates were found to be 16%(1 h),53%(6 h),and 84%(24 h),respectively.Notably,the self-made sustained-release suspension exhibited an extended half-life(21.518 h),delayed time to peak concentration(T_(max))(6 h),and reduced maximum plasma concentration(C_(max))(0.397μg/mL)in comparison to commercial granules(half-life=8.466 h;T_(max)=2 h;C_(max)=0.631μg/mL).Additionally,the area under the curve(AUC)indicated that the bioavailability of the self-made OP suspension surpassed that of the commercial OP granules by 101%.These findings underscored the successful development of an oral OP sustained-release suspension characterized by stability,tastelessness,ease of swallowing,convenient administration,and sustained-release properties,thereby potentially enhancing drug compliance among children.
基金the National Natural Science Foundation of China(No.52201066 and No.U21A2045)LiaoNing Revitalization Talents Program(NO.XLYC2002071)+2 种基金Gratitude is also expressed to the support from the Shanghai Aerospace Science and Technology Innovation Fund(SAST2020-046)the Fundamental Research Funds for the Central Universities(N2224002-21)the Natural Science Foundation of Shanghai(20ZR1424200).
文摘In order to obtain a more protective phosphate conversion coating with a denser architecture,the nucleation kinetics of phosphate chemical conversion coating on Mg-Gd-Y-Zr magnesium alloy was tuned in this work.A pretreatment process was proposed and organic additives were incorporated,which aims at increasing the ionic produce(J_(sp))at the interface for increasingσ,and decreasing the critical ionic product(J_(C,sp)),respectively.Results prove that the pretreatment of bare alloys in a phosphate bath could increase the ion products of MgHPO_(4)/MnHPO_(4).The addition of benzalkonium chloride could neutralize the charges of crystals,and in turn promote the nucleation kinetics.A denser and more protective conversion coating could consequently be obtained.
基金the financial support from China Youth Science Foundation(22207037).
文摘Inorganic phosphate(Pi)homeostasis in plants is regulated by inositol pyrophosphates(PP-InsPs),which mediate phosphate starvation responses.While beneficial microorganisms,such as arbuscular mycorrhizal fungi,contribute to phosphate uptake,pathogenic fungi often exploit phosphate metabolism to enhance virulence.However,the exact mechanisms by which pathogens manipulate plant phosphate signaling remain largely unknown.Here,we highlight a recent study by Ulrich Schaffrath and colleagues(Science,2025)revealing that plant pathogenic fungi deploy conserved Nudix hydrolase effectors to hydrolyze PP-InsPs,thereby mimicking phosphate starvation and suppressing host immunity.These findings not only expand our understanding of plantpathogen interactions,but also open new avenues for crop protection and resistance breeding.
基金supported by the National Natural Science Foundation of China(No.81802917 and No.82102969)the Huai’an Natural Science Research Program(No.HAB202101).
文摘Objective Nicotinamide adenine dinucleotide phosphate(NADPH)oxidases(NOXs)are known as major sources of reactive oxygen species(ROS),yet their role in regulating cellular antioxidative metabolism and ferroptosis is unclear.This study assessed the expression and clinical relevance of NOXs across pan-cancer and investigated the role of NOX4 in colorectal cancer progression Methods We analyzed transcriptomic and survival data from The Cancer Genome Atlas(TCGA)for NOXs across 22 types of solid tumors.A CRISPR library targeting NOXs was developed for potential therapeutic target screening in colorectal cancer cells(CRCs).Techniques such as CRISPR-knockout cell lines,1,2-13C-glucose tracing,PI staining,BrdU assays,and coimmunoprecipitation were employed to elucidate the function of NOX4 in CRCs.Results NOX4 emerged as a key therapeutic target for colorectal cancer from TCGA data.CRISPR screening highlighted its essential role in CRC survival,with functional experiments confirming that NOX4 upregulation promotes cell survival and proliferation.The interaction of NOX4 with glucose‑6‑phosphate dehydrogenase(G6PD)was found to enhance the pentose phosphate pathway(PPP),facilitating ROS clearance and protecting CRCs against ferroptosis.Conclusions This study identified NOX4 as a novel ferroptosis suppressor and a therapeutic target for the treatment of colorectal cancer.The findings suggest that a coupling between NADPH oxidase enzyme NOX4 and the PPP regulates ferroptosis and reveal an accompanying metabolic vulnerability for therapeutic targeting in colorectal cancer.
