Enhancing the stability of Ni Fe-layered double hydroxide nanosheet array for alkaline seawater oxidation by Ce doping

Electrocatalytic hydrogen production from seawater holds enormous promise for clean energy generation.Nevertheless,the direct electrolysis of seawater encounters significant challenges due to poor anodic stability caused by detrimental chlorine chemistry.Herein,we present our recent discovery that the incorporation of Ce into Ni Fe layered double hydroxide nanosheet array on Ni foam(Ce-Ni Fe LDH/NF)emerges as a robust electrocatalyst for seawater oxidation.During the seawater oxidation process,CeO_(2)is generated,effectively repelling Cl^(-)and inhibiting the formation of Cl O-,resulting in a notable enhancement in the oxidation activity and stability of alkaline seawater.The prepared Ce-Ni Fe LDH/NF requires only overpotential of 390 m V to achieve the current density of 1 A cm^(-2),while maintaining long-term stability for 500 h,outperforming the performance of Ni Fe LDH/NF(430 m V,150 h)by a significant margin.This study highlights the effectiveness of a Ce-doping strategy in augmenting the activity and stability of materials based on Ni Fe LDH in seawater electrolysis for oxygen evolution.

基于单颗粒电感耦合等离子体质谱法测定环境基质水样中纳米银颗粒

采用单颗粒电感耦合等离子体质谱法(SP-ICP-MS)同时测定环境水样中纳米银颗粒(AgNPs)的颗粒浓度、质量浓度和粒径分布,并考察了溶液的pH值、溶解性有机质(DOM)浓度以及离子强度等对AgNPs测定的影响。结果表明:SP-ICP-MS方法对60 nm AgNPs标准溶液的测定结果与标准值一致,准确性较好;pH值(5.0~7.0)、离子强度(≤1 mmol/L)和DOM浓度(≤30 mg/L)对测定结果影响较小;当溶液的pH值≤5.0或离子强度>1 mmol/L时,AgNPs的颗粒浓度和粒径随pH值的下降或离子强度的增强而减小。采用SP-ICP-MS方法测定河水、染料废水、养殖废水3种水样中AgNPs的加标回收率分别为98.1%、83.3%和93.3%,表明该方法在合适的基质条件下可用于快速准确测定环境水样中AgNPs的颗粒浓度、质量浓度和粒径分布。

电热解-塞曼原子吸收光谱法快速测定南药中总汞

建立了热解-塞曼原子吸收光谱法测定南药中总汞的快速分析方法。样品冻干后,利用热解技术直接测定南药固体样品中的汞,并利用塞曼效应对杂质信号进行背景校正,提高了测量的灵敏度。方法检出限为0.96μg·kg^(-1),定量限为3.18μg·kg^(-1),线性范围为0~15ng,线性相关系数r^2=0.9999。对4种标准物质进行分析,相对标准偏差(RSD)为2.4%~4.7%,表明该方法具有较高的准确度和精密度。经对实际样品分析,8种南药样品汞含量为5.22~25.30μg·kg^(-1),加标回收率90.6%~106.6%,RSD为1.1%~5.7%,该测定结果与热分解齐化原子吸收光谱法和微波消解-ICP-MS的检测结果基本一致。该方法准确、可靠,定量限满足《中国药典》(2015版)中的汞限量要求,可用于南药质量控制。

傅立叶变换离子回旋共振质谱用于金属加工助剂中的成分分析

金属加工助剂是金属加工生产过程中必不可少的化工产品,其组成复杂,易形成螯合物干扰成分分析。该文利用傅立叶变换离子回旋共振质谱(Fourier transform ion cyclotron resonance mass spectrometry,FT-ICR MS)技术的高分辨性能,结合电感耦合等离子体质谱(ICP-MS)、红外光谱(IR)和核磁共振谱(NMR)对一种含未知成分的金属加工助剂进行成分分析。结果表明,该金属加工助剂中含有柠檬酸钠、乙二胺四乙酸(EDTA)与金属铋螯合物。该方法简便、准确,适用于含有金属螯合物的金属加工助剂成分的快速鉴定。

傅里叶变换衰减全反射红外光谱分析塑料的润滑剂

研究傅里叶变换衰减全反射红外光谱(ATR-FTIR)在塑料润滑剂分析中的应用。结果表明,通过 ATR-FTIR 法可以快速分析塑料的润滑剂。

Co-doped Ni_(3)S_(2) nanosheet array: A high-efficiency electrocatalyst for alkaline seawater oxidation

Developing efficient and durable oxygen evolution reaction(OER)catalysts holds great promise for green hydrogen production via seawater electrolysis,but remains a challenge.Herein,we report a Co-doped Ni_(3)S_(2) nanosheet array on Ni foam(Co-Ni_(3)S_(2)/NF)as a high-efficiency OER electrocatalyst for seawater.In alkaline conditions,Co-Ni_(3)S_(2)/NF requires an overpotential of only 368 mV to drive 100 mA·cm^(–2),superior to Ni_(3)S_(2)/NF(385 mV).Besides,it exhibits at least 50-h continuous electrolysis.

Enhancing alkaline water oxidation with NiFe alloy-encapsulated nitrogen-doped vertical graphene array

Advancing efficient and affordable electrocatalysts to boost the oxygen evolution reaction(OER)is pivotal for sustainable green hydrogen production.Herein,we propose the fabrication of nickel-iron alloy nanoparticles-encapsulated on N-doped vertically aligned graphene array on carbon cloth(NiFe@NVG/CC)as a highly active three-dimensional(3D)catalyst electrode for OER.In 1 M KOH,such NiFe@NVG/CC demonstrates outstanding catalytic performance,necessitating merely overpotential of 245 mV for achieving a current density of 10 mA·cm^(−2),a remarkably low Tafel slope of 36.2 mV·dec^(−1).Furthermore,density functional theory calculations validate that the incorporate of N species into graphene can reinforce the electrocatalytic activity though reducing the reaction energy barrier during the conversion of*O to*OOH intermediates.The outstanding performance and structural benefits of NiFe@NVG/CC offer valuable insights for the development of innovative and efficient electrocatalysts for water oxidation.

Viscosity reduction of tapioca starch by incorporating with molasses hydrocolloids

As a low cost non-staple food resource,the high-viscosity paste and poor gel-forming ability of tapioca starch limit its industrial application.Herein,molasses hydrocolloids that is a by-product of the sugar refining process was applied as a blending modifier to reduce the viscosity of tapioca starch paste.The test results of paste and rheological properties show that molasses hydrocolloids exhibited a good physical viscosity-reducing effect on tapioca starch paste.The irregular network structure and high K^(+)/Ca^(2+)ion contents of molasses hydrocolloids exerted wrapping,adhesion,barrier,and hydration effects on starch,leading to the reduction of viscosity.The scanning electron microscope images and textural analysis demonstrated that this strategy also improve the structure of tapioca starch gel and enhanced its puncture strength by 75.46%.This work shows the great potential of molasses hydrocolloids as a lowcost and desirable material for the viscosity reduction of tapioca starch.

Ambient electrosynthesis of urea from carbon dioxide and nitrate over Mo_(2)C nanosheet

Electrocatalytic synthesis of urea through C-N bond formation,converting carbon dioxide(CO_(2))and ni-trate(NO_(3)^(-)),presents a promising,less energy-intensive alternative to industrial urea production process.In this communication,we report the application of Mo_(2)C nanosheets-decorated carbon sheets(Mo_(2)C/C)as a highly efficient electrocatalyst for facilitating C-N coupling in ambient urea electrosynthesis.In CO_(2)-saturated 0.2 mol/L Na_(2)SO_(4)solution containing 0.05 mol/L NO_(3)^(-),the Mo_(2)C/C catalyst achieves an impres-sive urea yield of 579.13μg h^(-1)mg^(-1)with high Faradaic efficiency of 44.80%at-0.5 V versus the reversible hydrogen electrode.Further theoretical calculations reveal that the multiple Mo active sites enhance the formation of^(∗)CO and^(∗)NH_(2)intermediates and facilitate their C-N coupling.This research propels the use of Mo_(2)C-based electrodes in electrocatalysis and accentuates the capabilities of binary metal-based catalysts in C-N coupling reactions.

Design and test of a double compression seeder for pre-sowing and seed furrow of wheat in wide-seedling belts

To solve the problem of poor sowing quality due to loose soil in wheat seedbed after land preparation in the Huang-Huaihai region of China,a double compression seeder for pre-sowing and seed furrow of wheat in wide-seedling belts was designed.The machine sowing operation was divided into two processes:pre-sowing compression and seed ditch compression,pre-sowing compression was carried out homogenization of the pre-sowing seed bed that the tractor wheel has crushed,and the seed ditch compression compresses the seeds and soil in the seed ditch,so that the seeds were embedded in the seed ditch soil.By analyzing the kinematics of the pre-planting compression device and the spiral blade in the process of soil levelling and compression,the structure of the equal-difference variable-diameter equal-pitch spiral conveying winch was designed,and the key parameters of the drum spiral blade were determined,and then the height of the spiral blades,the rutting distance and the speed of the compression roller were taken as the test factors,and the soil flatness was used as the index to carry out the discrete element simulation test.The simulation results show that when the spiral blade was 4.85 cm,the rut distance was 37.4 cm,and the rotation speed was 327.16 r/min,the optimal land flatness was 0.18.Finally,field experiments were carried out on the seeder,and the results showed that:the soil bulk density after operation was 22.7%greater than that before sowing(p<0.01),and the soil flatness was 1.9 cm,which was consistent with the simulated results.The use of pre-sowing compression and seed furrow compression methods improved the soil environment of the seed bed,increased the uniformity of the seeding depth,and promoted the root growth of wheat.This study provides equipment support and technical reference for agricultural production in wheat-corn rotation areas in the Huang-Huaihai region of China.

Shellac-coated iron oxide nanoparticles for removal of cadmium(Ⅱ) ions from aqueous solution

This study describes a new effective adsorbent for cadmium removal from aqueous solution synthesized by coating a shellac layer, a natural biodegradable and renewable resin with abundant hydroxyl and carboxylic groups, on the surface of iron oxide magnetic nanoparticles. Transmission Electron Microscopy （TEM） imaging showed shellac-coated magnetic nanoparticle （SCMN） adsorbents had a core-shell structure with a core of 20 nm and shell of 5 nm. Fourier Transform Infrared Spectroscopic analysis suggested the occurrence of reaction between carboxyl groups on the SCMN adsorbent surface and cadmium ions in aqueous solution. Kinetic data were well described by pseudo second-order model and adsorption isotherms were fitted with both Langmuir and Freundlich models with maximum adsorption capacity of 18.80 mg]g. SCMN adsorbents provided a favorable adsorption capacity under high salinity conditions, and cadmium could easily be desorbed using mild organic acid solutions at low concentration.

Antimony salt-promoted cyclization facilitating on-DNA syntheses of dihydroquinazolinone derivatives and its applications

DNA-encoded chemical libraries technology has become a novel approach to finding hit compounds in early drug discovery.The chemical space in a DEL would be expanded to realize its full potential,especially when integrating privileged scaffold dihydroquinazoline that has demonstrated a variety of diverse bioactivities.Driven by the requirement of parallel combinatorial synthesis,we here report a facile synthesis of on-DNA dihydroquinazolinone from aldehyde and anthranilamide.This DNA-compatible reaction was promoted by antimony trichloride,which has been proven to accelerate the reaction and improve conversions.Notably,the broad substrate scope of aldehydes and anthranilamides was explored under the mild reaction condition to achieve moderate-to-excellent conversion yields.We further applied the reaction into on-DNA macrocyclization,obtaining macrocycles embedded dihydroquinazolinone scaffold in synthetically useful conversion yields.

Erosive Pustular Dermatosis of the Scalp After Excision and Skin Grafting of Scalp Squamous Cell Carcinoma

Introduction:Erosive pustular dermatosis of the scalp(EPDS)is an uncommon condition with unknown etiology.The clinical exclusive diagnosis needs to be differentiated from similar diseases.Case presentation:A 68-year-old woman presented with an eight-month history of a chronic scalp eruption.She had been diagnosed as squamous cell carcinoma by biopsy nine months ago,and had been treated by surgical excision and skin grafting.One month later,she was referred for evaluation of the newly enlarged lesion which was observed at the skin grafting site.She was diagnosed of EPDS based on characteristics of lesions,clinicopathological findings and laboratory data.The condition had clinically improved with systemic steroid therapy and topical tacrolimus for two weeks.Relapses occurred after complete withdrawal of both treatments.After repeating the above therapy and applying topical tacrolimus as maintenance therapy,the condition was well controlled at the one-year follow-up.Discussion:EPDS is an uncommon inflammatory dermatosis with main incidence rate of elderly patients and female predominance.The diagnosis of EPDS cant be made only by histopathological examination,which is helpful for differential diagnosis.Microbiological investigations commonly remain negative.For the high risk of relapse,it is important for clinicians to be aware of maintenance treatment and a long-term management.Conclusion:It should be recognized by clinicians that EPDS is an uncommon and relapse disease,leading to serious cosmetic problems.The treatment lacks evidence-based medicine data,clinician should choose the appropriate therapy according to the condition of patients.

Fe-doped Co_(3)O_(4) nanowire strutted 3D pinewood-derived carbon: A highly selective electrocatalyst for ammonia production via nitrate reduction

Nitrate(NO_(3)^(-)),a nitrogen-containing pollutant,is prevalent in aqueous solutions,contributing to a range of environmental and health-related issues.The electrocatalytic reduction of NO_(3)^(-)holds promise as a sustainable approach to both eliminating NO_(3)^(-)and generating valuable ammonia(NH_(3)).Nevertheless,the reduction reaction of NO_(3)^(-)(NO_(3)^(-)RR),involving 8-electron transfer process,is intricate,necessitating highly efficient electrocatalysts to facilitate the conversion of NO_(3)^(-)to NH_(3).In this study,Fe-doped Co_(3)O_(4) nanowire strutted three-dimensional(3D)pinewood-derived carbon(Fe-Co_(3)O_(4)/PC)is proposed as a high-efficiency NO_(3)^(-)RR electrocatalyst for NH_(3) production.Operating within 0.1 M NaOH containing NO_(3)^(-),Fe-Co_(3)O_(4)/PC demonstrates exceptional performance,obtain an impressively large NH_(3) yield of 0.55 mmol·h^(-1)·cm^(-2) and an exceptionally high Faradaic efficiency of 96.5%at-0.5 V,superior to its Co_(3)O_(4)/PC counterpart(0.2 mmol·h^(-1)·cm^(-2),73.3%).Furthermore,the study delves into the reaction mechanism of Fe-Co_(3)O_(4) for NO_(3)^(-)RR through theoretical calculations.

An amorphous FeMoO_(4) nanorod array enabled high-efficiency oxygen evolution electrocatalysis in alkaline seawater

The development of highly efficient and durable oxygen evolution reaction(OER)catalysts for seawater electrolysis is of great importance for applications.Here,an amorphous FeMoO_(4) nanorod array on Ni foam is reported as a highly active OER electrocatalyst in alkaline seawater,requiring only overpotentials of 303 and 332 mV to achieve 100 and 300 mA·cm^(-2),respectively.Moreover,it shows strong long-term electrochemical durability for at least 50 h.

Cauliflower-like Ni_(3)S_(2) foam for ultrastable oxygen evolution electrocatalysis in alkaline seawater

It is of great importance to design and develop electrocatalysts that are both long-lasting and efficient for seawater oxidation.Herein,a three-dimensional porous cauliflower-like Ni_(3)S_(2) foam on Ni foam(Ni_(3)S_(2) foam/NF)is proposed as a high-performance electrocatalyst for the oxygen evolution reaction in alkaline seawater.The as-synthesis Ni_(3)S_(2) foam/NF achieves exceptional efficacy,achieving a current density of 100 mA·cm^(−2)at mere overpotential of 369 mV.Notably,its electrocatalytic stability extends up to 1000 h at 500 mA·cm^(−2).

Ultrasmall,elementary and highly translational nanoparticle X-ray contrast media from amphiphilic iodinated statistical copolymers

To expand the single-dose duration over which noninvasive clinical and preclinical cancer imaging can be conducted with high sensitivity,and well-defined spatial and temporal resolutions,a facile strategy to prepare ultrasmall nanoparticulate X-ray contrast media(nano-XRCM)as dual-modality imaging agents for positron emission tomography(PET)and computed tomography(CT)has been established.Synthesized from controlled copolymerization of triiodobenzoyl ethyl acrylate and oligo(ethylene oxide)acrylate monomers,the amphiphilic statistical iodocopolymers(ICPs)could directly dissolve in water to afford thermodynamically stable solutions with high aqueous iodine concentrations(>140 mg iodine/mL water)and comparable viscosities to conventional small molecule XRCM.The formation of ultrasmall iodinated nanoparticles with hydrodynamic diameters of ca.10 nm in water was confirmed by dynamic and static light scattering techniques.In a breast cancer mouse model,in vivo biodistribution studies revealed that the64Cu-chelator-functionalized iodinated nano-XRCM exhibited extended blood residency and higher tumor accumulation compared to typical small molecule imaging agents.PET/CT imaging of tumor over 3 days showed good correlation between PET and CT signals,while CT imaging allowed continuous observation of tumor retention even after 10 days post-injection,enabling longitudinal monitoring of tumor retention for imaging or potentially therapeutic effect after a single administration of nano-XRCM.

CoSe_(2)nanowire array enabled highly efficient electrocatalytic reduction of nitrate for ammonia synthesis

The electrocatalytic reduction of nitrate(NO_(3)^(-))not only facilitates the environmentally sustainable production of ammonia(NH_(3))but also purifies water by removing NO_(3)^(-),thereby transforming waste into valuable resources.The process of converting NO_(3)^(-)to NH_(3)is complex,involving eight electron transfers and multiple intermediates,making the choice of electrocatalyst critical.In this study,we report a cobalt selenide(Co Se_(2))nanowire array on carbon cloth(CoSe_(2)/CC)as an effective electrocatalyst for the NO_(3)^(-)to NH_(3)conversion.In an alkaline medium with 0.1 mol/L NO_(3)^(-),CoSe_(2)/CC demonstrates exceptional NH_(3)Faradaic efficiency of 97.6%and a high NH_(3)yield of 517.7μmol h^(-1)cm^(-2)at-0.6 V versus the reversible hydrogen electrode.Furthermore,insights into the reaction mechanism of CoSe_(2)in the electrocatalytic NO_(3)^(-)reduction are elucidated through density functional theory calculations.

Significantly enhanced ion-migration and sodium-storage capability derived by strongly coupled dual interfacial engineering in heterogeneous bimetallic sulfides with densified carbon matrix

The development of highly efficient sodium-ion batteries depends critically on the successful exploitation of advanced anode hosts that is capable of overcoming sluggish reaction kinetics while also withstanding severe structural deformation triggered by the large radius of Na^(+)-insertion.Herein,a hierarchically hybrid material with hetero-Co_(3)S_(4)/NiS hollow nanosphere packaged into a densified N-doped carbonmatrix(Co_(3)S_(4)/NiS@N-C)was designed and fabricated utilizing CoNi-glycerate as the self-sacrifice template,making the utmost of the synergistic effect of hetero-Co_(3)S_(4)/NiS with strong electric field and rich reaction active-sites together with the densified outer-carbon scaffolds with remarkable electronic conductivity and robust mechanical toughness.As anticipated,as-fabricated Co_(3)S_(4)/NiS@N-C anode affords remarkable specific capacity,prolonged cycle lifespan up to 2400 cycles with an only 0.05%fading each cycle at 20.0 A g^(−1),and excellent rate feature(354.9 mAh g^(−1)at 30.0 A g^(−1)),one of the best performances for most existing Co_(3)S_(4)/NiS-based anodes.Ex situ structural characterizations in tandem with theoretical analysis demonstrate the reversible insertion-conversion mechanism of initially proceeding with Na^(+)de-/intercalation and superior heterogeneous interfacial reaction behavior with strong Na^(+)-adsorption ability.Further,sodium-ion full cell and hybrid capacitor based on Co_(3)S_(4)/NiS@N-C anode exhibit impressive electrochemical characteristics on cycling performance and rate capability,showcasing its outstanding feasibility toward practical use.