Atomically dispersed Ni electrocatalyst for superior urea-assisted water splitting

Urea oxidation reaction(UOR) has been selected as substitution for oxygen evolution reaction ascribing to its low thermodynamic voltage as well as utilization of nickel as electrocatalyst.Herein,we report the formation of nickel single atoms(Ni-SAs) as exceptional bifunctional electrocatalyst toward UOR and hydrogen evolution reaction(HER) in urea-assisted water splitting.In UOR catalysis,Ni-SAs perform a superior catalytic performance than Ni-NP/NC and Pt/C ascribing to the formation of HOO-Ni-N_(4) structure evidenced by in-situ Raman spectroscopy,corresponding to a boosted mass activity by 175-fold at 1.4 V vs.RHE than Ni-NP/NC.Furthermore,Ni-SAs requires only 450 mV overpotential to obtain HER current density of 500 mA cm^(-2).136 mA cm^(-2) is achieved in urea-assisted water splitting at1.7 V for Ni-SAs,boosted by 5.7 times than Pt/C-IrO_(2) driven water splitting.

Inerting characteristics of entrained atomized water on premixed methane-air flame

A combustion tube experiment platform was designed and used to study the inerting conditions and capacity of entrained atomized water on premixed methane–air flame. The structure of a laminar flame of premixed methane–air gas and the process of interaction between atomized water and flame was recorded, and the rules of combustion velocity, stability and strength rate of laminar flame were experimentally studied. The inerting process and mechanism was analyzed, and the characteristics of inerting premixed methane–air gas within explosion limits by atomized water were acquired. The research results show that: for the premixed methane–air gas with a concentration of 7%, the minimum inerting atomized water flux is 20.8 m L/(m2min); for the premixed methane–air gas with a concentration of 9%, the minimum inerting atomized water flux is 32.9 m L/(m2min); for the premixed methane–air gas with a concentration of 11%, the minimum inerting atomized water flux is 44.6 m L/(m2min). The research results are significant for extinguishing methane flame and inhibiting of methane explosion using atomized water.

High-throughput calculation-based rational design of Fe-doped MoS_(2) nanosheets for electrocatalytic p H-universal overall water splitting

Electrocatalytic water splitting is crucial for H2generation via hydrogen evolution reaction(HER)but subject to the sluggish dynamics of oxygen evolution reaction(OER).In this work,single Fe atomdoped MoS_(2)nanosheets(SFe-DMNs)were prepared based on the high-throughput density functional theory(DFT)calculation screening.Due to the synergistic effect between Fe atom and MoS_(2)and optimized intermediate binding energy,the SFe-DMNs could deliver outstanding activity for both HER and OER.When assembled into a two-electrode electrolytic cell,the SFe-DMNs could achieve the current density of 50 mA cm^(-2)at a low cell voltage of 1.55 V under neutral condition.These results not only confirmed the effectiveness of high-throughput screening,but also revealed the excellent activity and thus the potential applications in fuel cells of SFe-DMNs.

Possibility of utilizing water-atomized Fe-Ni-Mo steel powder as base materials for warm compaction process

Water atomized Fe Ni Mo steel powder, was utilized as base powder for designing powder mixtures for warm pressing. The warm pressing and sintering behaviours of the powder mixtures were studied. The results show that, compared with the pressing at room temperature, the green density gain by warm pressing is within a range of 0.10 0.19 g/cm 3 and reduction in spring back is 30% 40% of the ambient, and maximum green density of 7.32 g/cm 3 at 735 MPa is obtained as the graphite mass fraction is 0.8%. It was found that sintered densities of the compacts were reduced slightly due to releasing of elastic stress stored in the compacts during sintering. The warm pressing of steel powders gives evidence for substituting the traditional double pressing and double sintering process.

Application of pre-alloyed powders for diamond tools by ultrahigh pressure water atomization

Copper, iron and cobalt based pre-alloyed powders for diamond tools were prepared by ultrahigh pressure water atomization（UPWA） process. Pre-alloyed powders prepared by different processes including UPWA, conventional water atomization （CWA） and elemental metal mechanical mixing （EMMM） were sintered to segments and then compared in mechanical properties, holding force between matrix and diamond, fracture morphology of blank and sintering diamond section containing matrix. The results showed that the pre-alloyed powder prepared by UPWA exhibits the best mechanical properties including the relative density, the hardness and the bending strength of matrix sinteredsegment. Sintered segments fractography of UPWA pre-alloyed powder indicatesmechanical mosaic strength and chemical bonding force between the pre-alloyed powder and the diamond, leading to the great increase in the holding force between matrix and diamond. The mechanical performance andthe service life of diamond tools were greatly improved by UPWA pre-alloyed powders.

Determination of Ultratrace Amounts of Copper(Ⅱ) in Water Samples by Electrothermal Atomic Absorption Spectrometry After Cloud Point Extraction

A novel approach was developed for the determination of ultratrace amounts of copper in water samples by using electrothermal atomic absorption spectrometry （ETAAS） after cloud point extraction （ CPE ）. 1-（ 2-Pyridylazo ） -2- naphthol was used as the chelating reagent and Triton X-114 as the mieellar-forming surfactant. CPE was conducted in a pH 8. 0 medium at 40 ℃ for 10 rain. After the separation of the phases by contrifugafion, the surfactant-rieh phase was diluted with 1 mL of a methanol solution of 0. 1 mol/L HNO3. Then 20μL of the diluted surfactant-rieh phase was injected into the graphite furnace for atomization in the absence of any matrix modifier. Various experimental conditions that affect the extraction and atomization processes were optimized. A detection limit of 5 ng/L was obtained after preconeentration. The linear dynamic range of the copper mass concentration was found to be 0-2.0 ng/mL, and the relative standard deviation was found to be less than 3. 1% for a sample containing 1.0 ng/mL Cu （ Ⅱ ）. This developed method was successfully applied to the determination of uhratraee amounts of Cu in drinking water, tap water, and seawater samples.

Seepage effects of groundwater and its make-up water on triggering ground subsidence

The functioning mechanism of groundwater and its make-up water in the process of ground subsidence was studied from such three aspects as osmotic corrasion, osmotic pressure effect and concretion effect, As to osmotic corrasion, its forming conditions, mechanical mechanism and process were analyzed, As to osmotic pressure effect, it was mainly studied from hydrostatic pressurizing effect, sop softening effect and negative pressure sealing effect. Through concretion and saturation of soil, the factors of concretion settlement were analyzed. The results showed that both groundwater and its make-up water are important triggering factors to ground subsidence.

Effects of combinatorial water atomization on microstructures and properties of Cu-Sn powder

A couple of additional cooling nozzles were assembled under traditionalatomization nozzles in order to improve the process and produce the powder with fine microstructureand low oxygen. The influence of the process parameters on the properties of the powder wasinvestigated. The results show that finer powders with lower oxygen content and more irregular shapecan be achieved by combinatorial atomizing process comparing with normal one under the sameatomizing pressure.

Speciation of Dissolved Trace Nickel in Environmental Waters by On-Line Sonodigestion-Flow Injection Solid Phase Extraction Coupled to Flame Atomic Absorption Spectrometry

A simple on-line sonodigestion system was successfully used for breakdown organic nickel complexes in environmental waters acidified with diluted nitric acid prior to flow injection total dissolved nickel preconcentration in a microcolumn containing a chelating resin (Chelite Che with iminodiacetic acid groups) and determination by flame atomic absorption spectrometry. For the determination of the dissolved labile nickel fraction, microcolumns packed with the chelating resin were loaded in-situ with the sample without sample pH modification, and once in the laboratory were inserted in the flow injection device where nickel elution-detection was carried out. The performance of the chelating resin was investigated in order to elucidate its behavior in the presence of dissolved nickel species. The results obtained reveal that the resin, at the experimental employed conditions, retained only dissolved free nickel ions and nickel bound to weak complexes (labile fraction). The figures of merit for determinations in both nickel fractions are given and the obtained values are discussed. The speciation scheme is applied to the analysis of nickel in river and seawater samples collected in Galicia (Northwest, Spain). The results of fractionation showed that Ni are mainly in the dissolved labile fraction in river water, while in seawater samples analyzed was mainly present in the organic fraction.

Atomically Dispersed Dual‑Metal Sites Showing Unique Reactivity and Dynamism for Electrocatalysis

The real structure and in situ evolution of catalysts under working conditions are of paramount importance,especially for bifunctional electrocatalysis.Here,we report asymmetric structural evolution and dynamic hydrogen-bonding promotion mechanism of an atomically dispersed electrocatalyst.Pyrolysis of Co/Ni-doped MAF-4/ZIF-8 yielded nitrogen-doped porous carbons functionalized by atomically dispersed Co–Ni dual-metal sites with an unprecedented N8V4 structure,which can serve as an efficient bifunctional electrocatalyst for overall water splitting.More importantly,the electrocatalyst showed remarkable activation behavior due to the in situ oxidation of the carbon substrate to form C–OH groups.Density functional theory calculations suggested that the flexible C–OH groups can form reversible hydrogen bonds with the oxygen evolution reaction intermediates,giving a bridge between elementary reactions to break the conventional scaling relationship.

For more and purer hydrogen-the progress and challenges in water gas shift reaction

The water gas shift(WGS) reaction is a standard reaction that is widely used in industrial hydrogen production and removal of carbon monoxide. The improved catalytic performance of WGS reaction also contributes to ammonia synthesis and other reactions. Advanced catalysts have been developed for both high and low-temperature reactions and are widely used in industry. In recent years, supported metal nanoparticle catalysts have been researched due to their high metal utilization. Low-temperature catalysts have shown promising results, including high selectivity, high shift rates, and higher activity potential. Additionally, significant progress has been made in removing trace CO through the redox reaction in electrolytic cell. This paper reviews the development of WGS reaction catalysts, including the reaction mechanism, catalyst design, and innovative research methods. The catalyst plays a crucial role in the WGS reaction, and this paper provides an instant of catalyst design under different conditions. The progress of catalysts is closely related to the development of advanced characterization techniques.Furthermore, modifying the catalyst surface to enhance activity and significantly increase reaction kinetics is a current research direction. This review goals to stimulate a better understanding of catalyst design, performance optimization, and driving mechanisms, leading to further progress in this field.

Water equivalence of some 3D dosimeters:a theoretical study based on the effective atomic number and effective fast neutron removal cross section

Effective atomic numbers for photon energy absorption(ZPEA_(eff)) and their corresponding electron numbers (NPEA_(eff)), and effective macroscopic removal cross sections of fast neutrons(RR) were calculated for 27 different types of three-dimensional dosimeters, four types of phantom materials, and water. The values of ZPEA_(eff) and NPEA_(eff) were obtained using the direct method for energies ranging from 10 keV to 20 MeV. Results are presented relative to water, for direct comparison over the range of examined energies. The effect of monomers that are used in polymer gel dosimeters on the water equivalence is discussed. The relation between Σ_R and hydrogen content was studied. Micelle gel dosimeters are highly promising because our results demonstrate perfect matching between the effective atomic number, electron density number, and fast neutron attenuation coefficient of water.

Water Repellent Finishing on Cotton Fabric via Atom Transfer Radical Polymerization

In order to enhance the water repellence property of cotton fabric, cotton fabric was grafted using hexafluorobutyl methacrylate( HFMT) monomer via atom transfer radical polymerization( ATRP) method. Water repellent cotton fabric was successfully prepared, and characterized by scanning electron microscopy( SEM),Fourier transform infrared spectroscopy( FTIR), and X-ray photoelectron spectroscopy( XPS). The SEM images of the HFMT-treated cotton displayed significant difference from the untreated one. FT-IR characterization of the HFMTtreated cotton indicated that HFMT was successfully grafted onto the surface of the cotton fabric. XPS analysis indicated that the fluorine element of the HFMT-treated cotton existing on the surface of the cotton fabric. The surface contact angle test as well as the water repellence rating test showed that the water repellence of the HFMTtreated cotton fabric was much better than that of the untreated cotton fabric. The surface contact angle of the HFMT-treated cotton fabric could reach( 132. 4 ± 2. 2) °,and the water repellence rating could achieve grade 3. The washing durability of the HFMT-treated fabric was also investigated. The surface contact angle of the HFMTtreated cotton fabric could reach( 121. 1 ± 2. 1) ° after 20 washing times. Furthermore, the whiteness, air permeability, breaking strength,and breaking elongation of the HFMT-treated cotton fabric decreased slightly compared with the untreated cotton fabric.Finally,cotton fabric with good water repellence property and excellent washing durability could be obtained with little effect on the intrinsic properties of cotton fabric.

Electronic Coupling of Single Atom and FePS_3 Boosts Water Electrolysis

Engineering the electronic structure of surface active sites at the atomic level can be an efficient way to modulate the reactivity of catalysts.Herein,we report the rational tuning of surface electronic structure of FePS_(3) nanosheets(NSs)by anchoring atomically dispersed metal atom.Theoretical calculations predict that the strong electronic coupling effect in single-atom Ni-FePS_(3) facilitates electron aggregation from Fe atom to the nearby Ni-S bond and enhances the electron-transfer of Ni and S sites,which balances the oxygen species adsorption capacity,reinforces water adsorption and dissociation process to accelerate corresponding oxygen evolution reaction(OER)and hydrogen evolution reaction(HER).The optimal Ni-FePS_(3)NSs/C exhibits outstanding electrochemical water-splitting activities,delivering an overpotential of 287 mV at the current density of 10 mA cm^(-2) and a Tafel slope of 41.1 mV dec^(-1) for OER;as well as an overpotential decrease of 219 mV for HER compared with pure FePS_(3)NSs/C.The concept of electronic coupling interaction between the substrate and implanted single active species offers an additional method for catalyst design and beyond.

Determination of Heavy Metals at Sub-ppb Levels in Water by Graphite Furnace Atomic Absorption Spectrometry Using a Direct Introduction Technique after Preconcentration with an Iminodiacetate Extraction Disk

A direct analysis method combining an iminodiacetate extraction disk (IED) with graphite furnace atomic absorption spectrometry was developed for the determination of Co, Ni, Cu, Cd, Sn, Pb, and Bi at sub-ppb levels in water. A 100 mL water sample was adjusted to pH 5.6 with nitric acid and a 1 mol?L–1 ammonium acetate solution, and then passed through an IED (diameter, 47 mm;effective filtering diameter, 35 mm) at a flow rate of 80 - 100 mL?min–1 to preconcentrate seven analytes. The IED was dried at 100?C for 20 min in an electric oven, and 110 - 145 small disks, each 2 mm in diameter, were punched out from the IED. A small disk was introduced into the graphite furnace and atomized according to a heating program. For Cd, Sn, Pb, and Bi measurements, Pd was used as a chemical modifier to enhance the absorbances. Calibration was performed using aqueous standard solutions. The detection limits, corresponding to three times the standard deviation (n = 5) of the blank values, were 0.092 μg·L–1 for Co, 0.12 μg·L–1 for Ni, 0.40 μg·L–1 for Cu, 0.077 μg·L–1 for Cd, 0.92 μg·L–1 for Sn, 0.61 μg·L–1 for Pb, and 0.80 μg·L–1 for Bi with an enrichment factor of 140 using a 100-mL water sample. A spike test for the seven analytes in tap water, rainwater, river water, and mineral drinking water showed quantitative recoveries (93% - 108%).

DETERMINATION OF ANTIMONY IN WATER SAMPLES BY FLOW-INJECTION HYDRIDE GENERATION ATOMIC ABSORPTION SPECTROMETRY WITH ON-LINE ION-EXCHANGE COLUMN PRECONCENTRATION

On-line ion-exchange separation and preconcentration were combined with flow-injection hydride generation atomic absorption spectrometry (HGAAS) to determine ultra-trace amounts of antimony in water samples. Antimony(Ⅲ) was preconcentrated on a micro-column packed with CPG-8Q chelating ion-exchanger using time-based sample loading and eluted by 4 mol l^(-1) HCl directly into the hydride generation AAS system. A detection limit (3σ) of 0.0015μg l^(-1) Sb(Ⅲ) was obtained on the basis of a 20 fold enrichment and with a sampling frequency of 60h^(-1). The precision was 1.0% r.s.d.(n=11) at the 0.5μg l^(-1) Sb(Ⅲ) level. Recoveries for the analysis of antimony in tap water, snow water and sea water samples were in the range 97-102%.

油水气混合的数字化微量润滑装置

微量润滑装置对油水气量的准确控制及其雾化效果,将直接影响切削冷却效果,进而影响零件加工质量。为改善微量润滑装置的辅助切削效果,研制了一种具有油水气混合的数字化微量润滑装置,有效改善了润滑油雾喷射的连续性和均匀性。基于微量润滑雾化技术,设计开发了数字化微量润滑装置,搭建铣削工艺实验平台,测试新型微量润滑装置的辅助切削效果。结果表明,所研制的油水气混合的数字化微量润滑装置能够明显提高油雾质量和辅助切削效果。

石墨炉原子吸收测定间接空冷机组循环水中的痕量铝

采用石墨炉原子吸收测定SCAL型间接空冷机组循环水中的痕量铝,从石墨炉工作参数、基体改进剂、试剂空白、水样前处理等方面进行了实验条件优选。实验结果表明:石墨炉灰化温度、原子化温度分别为700℃和2 700℃,不加基体改进剂条件下,铝离子标液质量浓度在0~20μg/L范围内标准曲线线性相关系数可达到0.999 8,相对标准偏差小于10%,检测下限为0.5μg/L。采用水样酸化静置1 h后直接测定并与标准加热消解法测定值进行了对比,相对误差小于5.0%,空白值小于0.5μg/L,有效解决了加热消解法空白值高的问题,提高了间接空冷机组循环水中小于10μg/L痕量铝测定的准确性。

基于超声波技术的矿井水井下预处理试验研究

混凝、沉淀(浮升)和过滤是矿井水的预处理方法,但设备占地面积大、耗费时间长、混凝剂与絮凝剂污染等问题一直制约着矿井水井下处理技术的进一步发展。为此,以现场采空区水样与岩样为研究对象,设计了一套基于超声波雾化技术的矿井水井下预处理装置,采用超声波雾化技术进行矿井水澄清与预软化处理,满足井下生产、消防及降尘用水需要。结果表明:(1)该方法可将黑灰色且有大量固体杂质悬浮物的浑浊矿井水澄清,有效去除水中难溶的固体杂质;(2)超声波雾化技术对水的总硬度降低72.24%,Ca^(2+)的质量浓度由试验前的5.33 mg/L降低到0.81 mg/L,Mg^(2+)的质量浓度由5.23 mg/L降低到2.13 mg/L,对pH值的影响较小;(3)经超声波雾化后的采空区水可满足井下消防洒水、喷淋降尘、采煤设备开采过程及冷却水的使用要求。

水浴消解-原子荧光法测定糖厂滤泥中的总砷和总汞

建立了采用水浴消解-原子荧光光度法测定糖厂滤泥中总砷和总汞含量的方法。试验结果表明,在最佳测试条件下,糖厂滤泥样品中总砷、总汞的线性浓度范围分别为0~100μg/L、0~2.00μg/L;总砷、总汞的检出限分别为0.012 mg/kg、0.001 mg/kg;精密度试验(n=9)总砷、总汞的相对标准偏差(RSD)分别为2.4%、3.8%;回收试验总砷、总汞的回收率分别为98.8%~107.9%、98.5%~107.2%。该方法准确度高,其精密度、检出限、回收率均能满足检测的要求,可为广西糖厂滤泥中总砷和总汞的含量测定及安全性评价提供参考。