Extending the solid solution range of sodium ferric pyrophosphate:Off‐stoichiometric Na_(3)Fe(2.5)(P_(2)O_(7))_(2)as a novel cathode for sodium‐ion batteries

Iron‐based pyrophosphates are attractive cathodes for sodium‐ion batteries due to their large framework,cost‐effectiveness,and high energy density.However,the understanding of the crystal structure is scarce and only a limited candidates have been reported so far.In this work,we found for the first time that a continuous solid solution,Na_(4−α)Fe_(2+α)_(2)(P_(2)O_(7))_(2)(0≤α≤1,could be obtained by mutual substitution of cations at center‐symmetric Na3 and Na4 sites while keeping the crystal building blocks of anionic P_(2)O_(7) unchanged.In particular,a novel off‐stoichiometric Na_(3)Fe(2.5)(P_(2)O_(7))_(2)is thus proposed,and its structure,energy storage mechanism,and electrochemical performance are extensively investigated to unveil the structure–function relationship.The as‐prepared off‐stoichiometric electrode delivers appealing performance with a reversible discharge capacity of 83 mAh g^(−1),a working voltage of 2.9 V(vs.Na^(+)/Na),the retention of 89.2%of the initial capacity after 500 cycles,and enhanced rate capability of 51 mAh g^(−1)at a current density of 1600 mA g^(−1).This research shows that sodium ferric pyrophosphate could form extended solid solution composition and promising phase is concealed in the range of Na_(4−α)Fe_(2+α)_(2)(P_(2)O_(7))_(2),offering more chances for exploration of new cathode materials for the construction of high‐performance SIBs.

Localized wave solutions and interactions of the (2+1)-dimensional Hirota-Satsuma-Ito equation

This paper studies the(2+1)-dimensional Hirota-Satsuma-Ito equation.Based on an associated Hirota bilinear form,lump-type solution,two types of interaction solutions,and breather wave solution of the(2+1)-dimensional Hirota-Satsuma-Ito equation are obtained,which are all related to the seed solution of the equation.It is interesting that the rogue wave is aroused by the interaction between one-lump soliton and a pair of resonance stripe solitons,and the fusion and fission phenomena are also found in the interaction between lump solitons and one-stripe soliton.Furthermore,the breather wave solution is also obtained by reducing the two-soliton solutions.The trajectory and period of the one-order breather wave are analyzed.The corresponding dynamical characteristics are demonstrated by the graphs.

Bifurcations, Analytical and Non-Analytical Traveling Wave Solutions of (2 + 1)-Dimensional Nonlinear Dispersive Boussinesq Equation

For the (2 + 1)-dimensional nonlinear dispersive Boussinesq equation, by using the bifurcation theory of planar dynamical systems to study its corresponding traveling wave system, the bifurcations and phase portraits of the regular system are obtained. Under different parametric conditions, various sufficient conditions to guarantee the existence of analytical and non-analytical solutions of the singular system are given by using singular traveling wave theory. For certain special cases, some explicit and exact parametric representations of traveling wave solutions are derived such as analytical periodic waves and non-analytical periodic cusp waves. Further, two-dimensional wave plots of analytical periodic solutions and non-analytical periodic cusp wave solutions are drawn to visualize the dynamics of the equation.

Efficient removal of Al(Ⅲ)and P507 from high concentration MgCl_(2)solution based on in-situ reaction strategy

For a highly efficient recycling of a wastewater containing a high concentration of MgCl_(2),Al(Ⅲ)and P507 were scheduled to be removed in advance.In this study,the in-situ removal of Al(Ⅲ)and P507 from a high concentration MgCl_(2)solution at different pH values and Al/P molar ratios was investigated.The results showed that P507 formed organic complexes of Al_(x)(OH)_y^(Z+)-P507 at pH of 2.0-4.0.At pH of 4.0-5.0,Al(Ⅲ)precipitated and transferred into Al(OH)_(3)with a flocculent amorphous morphology.Active sites on the Al(OH)_(3)surface enhanced the removal efficiency of P507.At pH of 6.0-6.5,Al(Ⅲ)and Mg(Ⅱ)formed layered crystalline Al(OH)_(3)and MgAl_(2)(OH)_(8with)small pore channels and fewer active sites,resulting in a reduced removal efficiency of P507.When the Al/P molar ratio exceeded 13 and the pH was between 4.0 and 5.0,the removal rates of both Al(Ⅲ)and P507 were higher than98%,while the concentration loss of Mg(Ⅱ)was only 0.2%-0.9%.

CO2 Transformation at Controlled Temperature with Lithium Hydroxide Solution and Metallic Lithium

This paper presents a study on CO2 atmospheric transformation which was reacted directly with lithium hydroxide solution and metallic lithium. This solution was obtained through the reaction between metallic lithium and deionized water where hydrogen is produced and by exposing the metal at ambient conditions. In the transformation process, atmospheric CO2 gas reacts directly with LiOH solution, in both cases, the CO2 transformation kinetics was different. For this purpose, reactions between CO2 and LiOH solution were carried out under controlled temperature and the second process only with metallic lithium, which was exposed at room temperature, however, in these two processes lithium carbonate oxide was formed and identified. According to the results, the efficiency in CO2 transformation is a function of temperature value which was variable until completely obtaining the by-product, its XRD characterization indicated the formation only of Li2CO3 in both procedures. Under laboratory conditions lithium compounds selectively reacted with CO2. In the same way, there is an alternative procedure to obtain LiOH and Li2CO3 for different applications in various areas.

In-situ exsolved ultrafine Ni nanoparticles from CeZrNiO_(2)solid solution for efficient photothermal catalytic CO_(2)reduction by CH4

CO_(2)reduction by CH4(CRM)to produce fuel is of great significance for solar energy storage and eliminating greenhouse gas.Herein,the catalyst of ultrafine Ni nanoparticles supported on CeZrNiO_(2)solid solution(Ni@CZNO)was synthesized by the sol-gel method.High yield of H_(2)and CO(58.0 and 69.8 mmol min^(-1)g^(-1))and excellent durability(50 h)were achieved by photothermal catalytic CRM merely under focused light irradiation.Structural characterization and DFT calculations reveal that CZNO has rich oxygen vacancies that can adsorb and activate CO_(2)to produce reactive oxygen species.Oxygen species are transferred to ultrafine Ni nanoparticles through the rich Ni-CZNO interface to accelerate carbon oxidation,thereby maintaining the excellent catalytic stability of the catalyst.Moreover,the experimental results reveal that light irradiation can not only enhance the photothermal catalytic CRM activity through photothermal conversion and molecular activation,but also improve the stability by increasing the concentration of oxygen vacancies and inhibiting CO disproportionation.

Ligand-free Cs2PdBr6 perovskite microcrystals with narrow bandgap and high photoelectrochemical performance in aqueous solution

The exploration of efficient lead-free perovskite photoelectric active materials to develop high-performance photoelectrochemical(PEC)systems in aqueous solution is crucial to expand their PEC applications.Herein,we successfully constructed a high-performance PEC platform using ligand-free perovskite Cs2PdBr6 microcrystals(MCs)as the photoactive substance.The Cs2PdBr6 MCs showed narrow bandgap,wide absorption range,high electronic mobility and good stability in aqueous solutions.Particularly,the Cs2PdBr6 MCs exhibited an excellent photoresponse,the photocurrent density could reach as high as 98μA/cm^(2)under 10.18 mW/cm^(2)light irradiation in the absence of other electron acceptors.In addition of the extremely wide range of response wavelength,wide pH range and accelerated interfacial carrier transfer,the Cs2PdBr6 MCs demonstrated the significant potential of photocathode active material for applications in PEC sensors and optoelectronic devices.Therefore,this work indicates that Cs2PdBr6 MCs design is a highly efficient way to solve the intrinsic issues of perovskite material,predicting a promising strategy for high performance PEC application in aqueous ambience.

Selective recovery of lead from zinc oxide dust with alkaline Na_2EDTA solution

The selective recovery of lead from the zinc oxide dust using an alkaline Na2EDTA solution was investigated. The effects of temperature, leaching time, Na2EDTA concentration and initial NaOH concentration on the leaching rates of lead and zinc were studied. The following optimized leaching conditions were obtained： liquid-to-solid ratio 5：1 mL/g, stirring speed 650 r/min, Na2EDTA concentration 0.12 mol/L, initial NaOH concentration 0.5 mol/L, leaching temperature 70 ℃, leaching time 120 min. Under the optimized conditions, the average leaching rates of lead, zinc, fluoride and chloride are 89.92%, 0.94%, 62.84% and 90.02%, respectively. The filtrate was used to electrowin lead powders. The average current efficiency of electrowinning is about 93% and lead content is higher than 98% under the conditions of temperature of 60 ℃, current density of 200 A/m2, H3PO4 concentration of 1.5 g/L, and lead ion concentration of above 5 g/L. The consumption of Na2EDTA and the direct current are about respectively 0.218 kg and 0.958 kW·h for per kilogram of lead powder.

Removal of S^(2-) ion from sodium aluminate solutions with sodium ferrite

The synthesis of sodium ferrite and its desulfurization performance in S2 -bearing sodium aluminate solutions were investigated. The thermodynamic analysis shows that the lowest temperature is about 810 K for synthesizing sodium ferrite by roasting the mixture of ferric oxide and sodium carbonate. The results indicate that the formation process of sodium ferrite can be completed at 1173 K for 60 min, meanwhile raising temperature and reducing NazCO3 particle size are beneficial to accelerating the formation of sodium ferrite. Sodium ferrite is an efficient desulfurizer to remove the S2- in aluminate solution, and the desulfurization rate can reach approximately 70% at 373 K for 60 min with the molar ratio of iron to sulfur of 1：1-1.5：1. Furthermore, the desulfurization is achieved by NaFeS2·2H2O precipitation through the reaction of Fe（OH）4 and S^2- in aluminate solution, and the desulfurization efficiency relies on the Fe（OH）4^- generated by dissolving sodium ferrite.

Influence of solution treatment on microstructure and properties of in-situ Mg_2Si/AZ91D composites

The influence of solution treatment on the microstructure and properties of Mg2Si/AZ91D composites fabricated from Mg-SiO2 system via in-situ processing method was investigated.The results show that coarse Chinese script shape Mg2Si phases can be formed by adding SiO2 into AZ91D magnesium alloy with Si content up to 1.5% of the alloy melt.During solution treatment,the morphology and distribution of the coarse Chinese script shape Mg2Si phases are modified.Meanwhile,the β-Mg17Al12 phase is dissolved into the magnesium matrix.With increasing holding time,the coarse Mg2Si phases tend to dissolve,break and spheroidize.After solution treatment at 420 ℃ for 16 h,Mg2Si phases become the finest and relatively well-distributed phase.The tensile strength and elongation are increased by 14.9% and 38.9%,respectively.It is believed that the Mg2Si phases continuously dissolve and break,and finally the spheroidized Mg2Si particles are obtained due to the interface tension of Mg2Si/Mg interface.

Measurements of zinc oxide solubility in sodium hydroxide solution from 25 to 100 °C

The solubility of zinc oxide in sodium hydroxide solution was measured in a closed polytetrafluoroethylene vessel from 25 to 100 ℃. The ZnO solubility was determined by employing the method of isothermal solution saturation. The results show that only ZnO solid exists in the equilibrium state in the low concentration alkali regions, and the solubility of zinc oxide is almost invariable with temperature. With the increase of alkali concentration, equilibrium solid turns from ZnO to NaZn（OH）3 suddenly, this mutation is called invariant point. The alkali concentration of the invariant points increases with increasing temperature, but the solubility of NaZn（OH）3 decreases with increasing alkali concentration at the same temperature. At the same Na2O concentration, the higher the temperature is, the higher the solubility of NaZn（OH）3 is.

Fabrication of Cu_2O@Cu_2O core-shell nanoparticles and conversion to Cu_2O@Cu core-shell nanoparticles in solution

Cu2O@Cu2O core-shell nanoparticles (NPs) were prepared by using solution phase strategy. It was found that Cu2O@Cu2O NPs were easily converted to Cu2O@Cu NPs with the help of polyvinylpyrrolidine (PVP) and excessive ascorbic acid (AA) in air at room temperature, which was an interesting phenomenon. The features of the two kinds of NPs were characterized by XRD, TEM and extinction spectra. Cu2O@Cu NPs with different shell thicknesses showed wide tunable optical properties for the localized surface plasmon (LSP) in metallic Cu. But Cu2O@Cu2O NPs did not indicate this feature. FTIR results reveal that Cu+ ions on the surface of Cu2O shell coordinate with N and O atoms in PVP and are further reduced to metallic Cu by excessive AA and then form a nucleation site on the surface of Cu2O nanocrystalline. PVP binds onto different sites to proceed with the reduction utill all the Cu sources in Cu2O shell are completely assumed.

Synthesis of nanostructured Li_2FeSiO_4/C cathode for lithium-ion battery by solution method

Nanosphere-like Li2FeSiO4/C was synthesized via a solution method using sucrose as carbon sources under a mild condition of time-saving and energy-saving, followed by sintering at high temperatures for crystallization. The amount of carbon in the composite is less than 10% （mass fraction）, and the X-ray diffraction result confirms that the sample is of pure single phase indexed with the orthorhombic Pmn21 space group. The particle size of the Li2FeSiO4/C synthesized at 700 °C for 9 h is very fine and spherical-like with a size of 200 nm. The electrochemical performance of this material, including reversible capacity, cycle number, and charge-discharge characteristics, were tested. The cell of this sample can deliver a discharge capacity of 166 mA-h/g at C/20 rate in the first three cycles. After 30 cycles, the capacity decreases to 158 mA-h/g, and the capacity retention is up to 95%. The results show that this method can prepare nanosphere-like Li2FeSiO4/C composite with good electrochemical performance.

Solution广泛多孔钛涂层长柄假体结合钢丝环扎固定治疗股骨头置换术后VancouverB2型假体周围骨折的中期随访

背景：股骨头置换术后Vancouver B2型假体周围骨折多伴有假体松动，患者年龄大，并存疾病多，骨质条件差，围手术期处理及手术技术难度大，并发症发生率高。 目的：评价Solution广泛多孔钛涂层长柄假体结合钢丝环扎固定治疗股骨头置换术后Vancouver B2型假体周围骨折的中期疗效。 方法：回顾分析2008年1月至2010年12月我科收治的14例股骨头置换术后Vancouver B2型假体周围骨折患者的临床资料，其中男6例，女8例，年龄66-80岁，平均70.3岁。所有患者均采用骨折切开复位钢丝环扎固定结合Solution股骨柄进行翻修手术。末次随访时进行Harris髋关节评分（术前由于骨折未能进行Harris髋关节评分）；术前，术后3、6、12个月及末次随访时摄X线片，用于评价骨折复位及愈合，假体初始固定及中期生存情况。 结果：共16例患者，1例术后3年死于肺癌，1例失访，14例获得随访，随访时间3-5年，平均4.2年。末次随访时Harris评分88.7分。X线显示骨折复位，股骨柄超过骨折远端的固定长度超过5 cm，与股骨压配良好。骨折愈合时间3-6个月，平均（3.8＆#177;1.3）个月。末次随访时未见股骨柄松动、下沉。无感染、深静脉血栓形成和肺栓塞。 结论：Solution股骨柄结合钢丝环扎固定治疗股骨头置换术后Vancouver B2型假体周围骨折中期疗效好，其远期结果有待于进一步的随访。

Solution combustion synthesis of Ni-Y_2O_3 nanocomposite powder

Ni-Y2O3 nanocomposite powder with uniform distribution of fine oxide particles in the metal matrix was successfully fabricated via solution combustion process followed by hydrogen reduction. The combustion behavior was investigated by DTA-TG analysis. The influence of urea to nickel nitrate（U/Ni） ratio on the combustion behavior and morphology evolution of the combusted powder was investigated. The morphological characteristics and phase transformation of the combusted powder and the reduced powder were characterized by FESEM, TEM and XRD. The HRTEM image of Ni-Y2O3 nanocomposite powder indicated that Y2O3 particles with average particle size of about 10 nm dispersed uniformly in the nickel matrix.

Modified (2+1)-dimensional displacement shallow water wave system and its approximate similarity solutions

Recently, a new （2＋1）-dimensional shallow water wave system, the （2＋1）-dlmenslonal displacement shallow water wave system （2DDSWWS）, was constructed by applying the variational principle of the analytic mechanics in the Lagrange coordinates. The disadvantage is that fluid viscidity is not considered in the 2DDSWWS, which is the same as the famous Kadomtsev-Petviashvili equation and Korteweg-de Vries equation. Applying dimensional analysis, we modify the 2DDSWWS and add the term related to the fluid viscidity to the 2DDSWWS. The approximate similarity solutions of the modified 2DDSWWS （M2DDSWWS） is studied and four similarity solutions are obtained. For the perfect fluids, the coefficient of kinematic viscosity is zero, then the M2DDSWWS will degenerate to the 2DDSWWS.

The Travelling Wave Solutions for （2＋1）-dimensional AKNS Equation

Based on the travelling wave method, a(2 + 1)-dimensional AKNS equation is considered. Elliptic solution and soliton solution are presented and it is shown that the soliton solution can be reduced from the elliptic solution. It also proves that the result is consistent with the soliton solution of simplify Hirota bilinear method by Wazwaz and illustrate the solution are right travelling wave solution.

SnO_2-based solid solutions for CH_4 deep oxidation: Quantifying the lattice capacity of SnO_2 using an X-ray diffraction extrapolation method

A series of SnO2‐based catalysts modified by Mn, Zr, Ti and Pb oxides with a Sn/M （M=Mn, Zr, Ti and Pb） molar ratio of 9/1 were prepared by a co‐precipitation method and used for CH4 and CO oxidation. The Mn3＋, Zr4＋, Ti4＋and Pb4＋cations are incorporated into the lattice of tetragonal rutile SnO2 to form a solid solution structure. As a consequence, the surface area and thermal stability of the catalysts are improved. Moreover, the oxygen species of the modified catalysts become easier to be reduced. Therefore, the oxidation activity over the catalysts was improved, except for the one modified by Pb oxide. Manganese oxide demonstrates the best promotional effects for SnO2. Using an X‐ray diffraction extrapolation method, the lattice capacity of SnO2 for Mn2O3 was 0.135 g Mn2O3/g SnO2, which indicates that to form stable solid solution, only 21%Sn4＋cations in the lattice can be maximally replaced by Mn3＋. If the amount of Mn3＋cations is over the capacity, Mn2O3 will be formed, which is not favorable for the activity of the catalysts. The Sn rich samples with only Sn‐Mn solid solution phase show higher activity than the ones with excess Mn2O3 species.

New exact periodic solutions to (2+1)-dimensional dispersive long wave equations

In this paper, we make use of the auxiliary equation and the expanded mapping methods to find the new exact periodic solutions for （2＋1）-dimensional dispersive long wave equations in mathematical physics, which are expressed by Jacobi elliptic functions, and obtain some new solitary wave solutions （m → 1）. This method can also be used to explore new periodic wave solutions for other nonlinear evolution equations.

Separation of ionic liquids from dilute aqueous solutions using the method based on CO_2 hydrates

Ionic liquids （ILs） have been regarded as the potential novel solvents for improved analytical- and process-scale separation methods.The development of methods for the recovery of ILs from aqueous solutions to escape contamination and recycle samples will ultimately govern the viability of ILs in the future industrial applications. Therefore, in this paper a new method for separation of ILs from their dilute aqueous solutions and simultaneously purification of water was proposed on the basis of the CO2 hydrate formation. For illustration, the dilute aqueous solutions with concentrations of ILs ranging from 2× 10^-3 mol% to 2×10^-1 mol% were concentrated. The results show that the separation efficiency is very impressive and that the new method is applicable to aqueous solutions of both hydrophobic and hydrophilic ILs. Compared to the literature separation method based on the supercritical CO2, the new method is applicable to lower concentrations, and more importantly, its operation condition is mild.