Influence of Al_(2)O_(3)/SiO_(2) Ratio on the Structure and Properties of Na^(+)/K^(+)Ion Exchange Na_(2)O-MgO-Al_(2)O_(3)-SiO_(2) Glasses

In this work,the structure,viscosity and ion-exchange process of Na_(2)O-MgO-Al_(2)O_(3)-SiO_(2) glasses with different Al_(2)O_(3)/SiO_(2) molar ratios were investigated.The results showed that,with increasing Al_(2)O_(3)/SiO_(2) ratio,the simple structural units Q_(1) and Q_(2) transformed into highly aggregated structural units Q_(3) and Q_(4),indicating the increase of polymerization degree of glass network.Meanwhile,the coefficient of thermal expansion decreased from 9.23×10^(-6)℃^(-1) to 8.88×10^(-6)℃^(-1).The characteristic temperatures such as melting,forming,softening and glass transition temperatures increased with the increase of Al_(2)O_(3)/SiO_(2) ratio,while the glasses working temperature range became narrow.The increasing Al_(2)O_(3)/SiO_(2) ratio and prolonging ion-exchange time enhanced the surface compressive stress(CS)and depth of stress layer(DOL).However,the increase of ion exchange temperature increased the DOL and decreased the CS affected by stress relaxation.There was a good linear relationship between stress relaxation and surface compressive stress.Chemical strengthening significantly improved the hardness of glasses,which reached the maximum value of(622.1±10)MPa for sample with Al_(2)O_(3)/SiO_(2) ratio of 0.27 after heat treated at 410℃for 2 h.

Defective layered Mn-based cathode materials with excellent performance via ion exchange for Li-ion batteries

Defective layered Mn-based materials were synthesized by Li/Na ion exchange to improve their electrochemical activity and Coulombic efficiency.The annealing temperature of the Na precursors was important to control the P3-P2 phase transition,which directly affected the structure and electrochemical characteristics of the final products obtained by ion exchange.The O3-Li_(0.78)[Li_(0.25)Fe_(0.075)Mn_(0.675)]O_(δ) cathode made from a P3-type precursor calcined at 700℃ was analyzed using X-ray photoelectron spectrometry and electron paramagnetic resonance.The results showed that the presence of abundant trivalent manganese and defects resulted in a discharge capacity of 230 mAh/g with an initial Coulombic efficiency of about 109%.Afterward,galvanostatic intermittent titration was performed to examine the Li^(+) ion diffusion coefficients,which affected the reversible capacity.First principles calculations suggested that the charge redistribution induced by oxygen vacancies(OV_(s))greatly affected the local Mn coordination environment and enhanced the structural activity.Moreover,the Li-deficient cathode was a perfect match for the pre-lithiation anode,providing a novel approach to improve the initial Coulombic efficiency and activity of Mn-based materials in the commercial application.

Pb(Ⅱ) biosorption using chitosan and chitosan derivatives beads: Equilibrium, ion exchange and mechanism studies

The study examined the adsorption of Pb（II） ions from aqueous solution onto chitosan, chitosan-GLA and chitosan-alginate beads. Several important parameters influencing the adsorption of Pb（II） ions such as initial pH, adsorbent dosage and different initial concentration of Pb（II） ions were evaluated. The mechanism involved during the adsorption process was explored based on ion exchange study and using spectroscopic techniques. The adsorption capacities obtained based on non–linear Langmuir isotherm for chitosan, chitosan-GLA and chitosan-alginate beads in single metal system were 34.98, 14.24 and 60.27 mg/g, respectively. However, the adsorption capacity of Pb（II） ions were reduced in the binary metal system due to the competitive adsorption between Pb（II） and Cu（II） ions. Based on the ion exchange study, the release of Ca2＋, Mg2＋, K＋ and Na＋ ions played an important role in the adsorption of Pb（II） ions by all three adsorbents but only at lower concentrations of Pb（II） ions. Infrared spectra showed that the binding between Pb（II） ions and the adsorbents involved mostly the nitrogen and oxygen atoms. All three adsorbents showed satisfactory adsorption capacities and can be considered as an efficient adsorbent for the removal of Pb（II） ions from aqueous solutions.

Adsorption of Ce(Ⅳ) Anionic Nitrato Complexes onto Anion Exchangers and Its Application for Ce(Ⅳ) Separation from Rare Earths(Ⅲ)

Ce （Ⅳ） nitrato complexes were adsorbed on two anion exchangers based on polyvinyl pyridine （PVP） and quatemized PVP incorporated into porous silica matrix. The effect of nitric acid concentration （0.5～6 mol·L^-1） and temperature （278 ～318 K） on Ce（ Ⅳ ） sorption efficiency was investigated. Sorption increased with increasing nitric acid concentration, indicating that [Ce（NO3）6]^2- complex is the main adsorbed Ce（Ⅳ） species. Oxidation of sorbents by adsorbed Ce （ Ⅳ ） species resulting in Ce （ Ⅲ ） release to the solution was observed. Pyridine based anion exchangers exhibited higher oxidation stability compared to the commercial strong base anion exchanger. Ce（ Ⅳ ） reduction was temperature dependent and obeyed pseudo-first-order reaction kinetics. Column separation of Ce （ Ⅳ ） from La （ Ⅲ ） and Y （ Ⅲ ） was carried out from 6 mol·L^-1 nitric acid with PVP based anion exchanger. Reasonable Ce （Ⅳ） breakthrough capacity （0.7 mol·kg^-1 PVP） was achieved. No remarkable decrease of capacity was observed within 3 consequent runs. In contrast, Ce （Ⅲ） leakage due to reduction decreased and breakthrough capacity slightly increased. This effect was more pronounced with increasing temperature. Regeneration with 0.1 mol·L^- 1 nitric acid was successful （recovery 100% ± 4% ） and Ce solution of high purity （ 〉 99.97% ） with respect to La and Y content was gained.

Study on the influence of humic acid of different molecular weight on basic ion exchange resin's adsorption capacity

In this paper, humic acid （HA） was ultra-filtered into different molecular weight sections and was characterized by multielement analysis, UV254/TOC, FT-IR and three-dimensional fluorescence spectrometric. Since humic acids of different molecular weights have different hydrophilic and molecular size, the maximum adsorption capacity of basic ion exchange resins appears on the humic acid whose molecular weight ranges from 6000 to 10,000 Da.

Synthesis, structure characterization, and ion exchange properties of a novel open-framework ecomaterial silicotitanate

A novel open-framework ecomaterial silicotitanate (Na_4Ti_4Si_3O_(10)) wassynthesized by a combination of solgel and hydrothermal methods. The investigation on ion exchangeproperties shows that Na_4Ti_4Si_3O_(10) exhibits high ad-sorption for cesium, i.e., K_d is as highas 60 000 mL/g in neutral solution. The crystal structure of Na_4Ti_4Si_3O_(10) was characterized byX-ray difiraction (XRD), scanning electronic microscope (SEM), transmission electron microscope(TEM), Raman spectrum, differential thermal and thermogravimetric analysis (DTA/TGA), inductivelycoupled plasma (ICP), and X fluorescence analysis. The compound is tetragonal, P4_2, a=b = 0.781 10nm, c = 1.196 45 nm, alpha =beta = gamma = 90 deg, Z = 4, and R^a = 0.041; Na_4Ti_4Si_3O_(10) has athree dimensional framework consisting of Ti-O octahedral clusters and Si-O tetrahedra. The resultsshow that Na_4Ti_4Si_3O_(10) has good chemical stability, thermal stability, and high cesium ionexchange capacity in the whole pH range.

A novel protein refolding method integrating ion exchange chromatography with artificial molecular chaperone

Artificial molecular chaperone （AMC） and ion exchange chromatography （IEC） were integrated, thus a new refolding method, artificial molecular chaperone-ion exchange chromatography （AMC-IEC） was developed. Compared with AMC and IEC, the activity recovery of lysozyme obtained by AMC-IEC was much higher in the investigated range of initial protein concentrations, and the results show that AMC-IEC is very efficient for protein refolding at high concentrations. When the initial concentration of lysozyme is 180 mg/mL, its activity recovery obtained by AMC-IEC is still as high as 76.6%, while the activity recoveries obtained by AMC and IEC are 45.6% and 42.4%, respectively.

Synthesis of Pb-Feldspar by Ion Exchange Reaction and Its Implications

Feldspar and Pb（NO3）2 were mixed and reacted at T=380℃ to synthesize Pb-feldspar. In the XRD （X-ray diffraction） pattern of the product, the d values （crystal lattice spacing） of the five peaks are 0.654, 0.342, 0.332, 0.327 and 0.257 nm. The XPS analysis results show that the binding energy of Pb 4f（7/2） in the feldspar was between 137.81-138.03 eV. Pb^2＋ can replace alkali and alkali earth cations in the feldspar structure through ion exchange reaction to form Pb-feldspar.

Study on the permselectivity of ion exchange membrane

Ion exchange membranes with high permselectivity (the character of separatingcations from anions or anions from cations) and high selectivity (the character of separatingcations or anions of different valencies) are important for electrodialysis process. The Donnanequilibrium theory, based on the equilibrium of ions and no electric field, can not exactly explainthe permselectivity of ion exchange membrane for ED process, since it is impossible to set up a ionexchange equilibrium between membrane and solution and to neglect the influence of electricaldriving force on ions during ED process. A novel model named 'anti-electric potential' isestablished to interpret the permselectivity of ion exchange membrane, according to thedetermination of electric potential between membranes and the variation of elements content insolutions and membranes. The results of experiment prove that the 'anti-electric potential' reallyexists within membranes. As for the selectivity, the results reveal that electric potential andhydration energy have great influence on the concentration and mobility of ions in membranes.

Modelling of graded index waveguide fabricated by ion exchange on Er^(3+) doped glass

A general numerical tool, based on thermal diffusion equation and full-vectorial eigen-mode equation, has been presented for the systematic analysis of graded index channel waveguide fabricated by ion exchange on Er^3＋ doped glass. Finite difference method with full-vectorial formulation （FV-FDM） is applied to solving the full-vectorial modes of graded index channel waveguide for the first time. The coupled difference equations based on magnetic fields in FV-FDM are derived from the Taylor series expansion and accurate formulation of boundary conditions. Hybrid nature of vectorial guided modes for both pump （980 nm） and signal light （1550 nm） are demonstrated by the simulation. Results show that the fabrication parameters of ion exchange, such as channel opening width and time ratio of second step to first step in ion exchange, have large influence on the properties of waveguide. By optimizing the fabrication parameters, maintenance of monomode for signal light and improvement of the gain dynamics can be achieved in Er^3＋ doped waveguide amplifier （EDWA） fabricated by ion exchange technique. This theoretical model is significant for the design and fabrication of EDWA with ion exchange technique. Furthermore, a single polarization EDWA, which operates at wavelength from 1528 nm to 1541 nm for HE polarization, is numerically designed.

Recovery of V_2O_5 from Bayer liquor by ion exchange

A new technology was developed to recover V2O5 from Bayer spent liquor by ion exchange.The experimental results show that in the conditions of 105℃ and 0.20-0.25 mass ratios between CaO in lime and Al2O3 in spent liquor, the precipitation rate of vanadium in Bayer liquor is more than 85%.The vanadium-bearing precipitation is leached by NaHCO3 solution.The leaching rate of vanadium can reach 85% in the conditions of 95℃, 40 g·L-1 of NaHCO3 concentration, and ventilating of CO2.The 201 × 7 type of resin has good adsorption effect on vanadium in the leaching solution.The adsorption rate is more than 94% with the flow rate of 0.09 mL·min-1·g-1 of leaching solution and the temperature of 40-50℃.By using 3 mol·L-1 of NaOH to desorb the saturated resin after adsorption at 40-50℃, a solution with more than 5 g·L-1 of V2O5 can be obtained.After roasting ammonium metavanadate that precipitates from the desorption solution when NH4Cl is added at the temperature of 500-550℃ for 2 h, V2O5 with more than 99% of purity is obtained.

Theoretical Study on the Mass Transfer of Metal Ions in Ion Exchange Process

The kinetics of ion exchange between Ca2+, Mg2+, Co(Ⅱ), Cu(Ⅱ),Ni(Ⅱ), Fe(Ⅲ), y3+ or Sm3+ , respectively, in 0.50 mol/L HC1 and H+ on macrorecticular sulfonic ion exchange resin and the kinetics of the same reactions (M -H exchange) when Mn(Ⅱ) coexisted in resin phase as accelerating ion were studied. The accelerating effect manifested and its rule are consistent with the accelerating effect theory based on the concept concerned with adsorption electrical double layer which has been suggested in a previous paper published.

Weak cation exchange 2 protein chip for detecting differentially expressed brainstem proteins in a rat model of closed traumatic brain injury

BACKGROUND： Studies have reported the combined use of two-dimensional gel electrophoresis and mass spectrometry to detect differentially expressed proteins in the rat brainstem following brain injury. However, the detected differential proteins often exhibit low sensitivity and high relative molecular weight. Although protein chip technology is thought to compensate for these inadequacies, no related studies or results have been reported. OBJECTIVE： To propose the application of weak cation exchange protein chips in combination with mass spectrometry for determining protein expression profiles and characteristics in the brainstem following closed brain injury. DESIGN, TIME AND SETTING： Randomized, controlled, animal experiments utilizing proteomics were performed from June 2007 to December 2008 in the Proteomics Laboratory, Medical College of Chinese People＇s Armed Police Force. MATERIALS： Weak cation exchange 2 protein chip, Ciphergen Proteinchip System （PBS-IIC）. METHODS： A total of 72 rats were randomly assigned to two groups： sham-surgery （n = 12） and injury （n = 60）. A closed traumatic brain injury model caused by falling object was replicated in the injury group, which was then subdivided into five subgroups according to different time points after injury： 4, 8, 12, 24, and 48 hours, with 12 rats in each subgroup. In the sham-surgery group, only the skin was removed and the stainless steel pad was fixed to the skull. MAIN OUTCOME MEASURES： The brain injury rats were sacrificed at 4, 8, 12, 24, and 48 hours after injury, respectively, and the control rats were sacrificed at 24 hours. Pathological changes in the brainstem were determined using hematoxylin-eosin staining, and differential protein expression in the brainstem was detected using a weak cation exchange 2 protein chip and protein chip reader. RESULTS： In the sham-surgery group, cells appeared normal. However, in the brain injury group, some brainstem neurons exhibited pyknosis, with reduced numbers of Nissl bodies in the cytoplasm swollen cell bodies and nuclei, irregular staining in the cytoplasm, and decreased numbers of neurons. Results from weak cation exchange 2 protein chip detection demonstrated that, compared with the sham-surgery group, the expression profiles of 2 proteins were altered in the brainstem of the injury group. At 12, 24, and 48 hours after injury, expression was increased （P 〈 0.01 ）. The mass charge ratio （M/Z） of 7 862 differentially expressed proteins was greater in the sham-surgery group compared with 12 and 24 hours after injury （P 〈 0.05）. CONCLUSION： The combined method of weak cation exchange 2 protein chip and mass spectrometry detected differential protein expression in the brainstem following closed brain injury in the rats, which suggested that closed brain injury induced altered protein expression profiles in the brainstem.

First-principle study of Ba isotopic fractionation during ion exchange processes

The potential utilization and development of the Ba isotope tool depend on an accurateδ^(137/134)Ba determination of the samples.During the chemical purification,whether the adsorption process on the surface of the ionexchange resin could lead to the Ba isotopic fractionation and the degree of fractionation directly influence the accurateδ^(137/134)Ba determination.In the present work,first-principles calculations based on the density functional theory were used to quantify the Ba isotopic equilibrium fractionation factor between the aqueous solution and the resin in the acid leaching process.By constructing and optimizing the geometric configurations of Ba-containing species,Ba(H_(2)O)_(n)^(2+),Ba(H_(2)O)_(n)Cl_(2),Ba(H_(2)O)_(n)(NO_(3))2,and the adsorbed Ba^(2+)on the surface of the resin,extracting the harmonic vibrational frequencies,we finally at 298 K obtained the fractionations,Δ^(137/134)Ba_(soln-ads)=0.07‰,Δ^(137/134)Ba_(Ba(H_(2)O)_(n)Cl_(2)-ads)=0.05‰,andΔ^(137/134)-Ba^(Ba(H_(2)O)_(n)(NO_(3))2-ads)=0.02‰.Overall,there were almost no Ba isotope fractionations during leaching.Although the Ba isotope fractionation can be magnified by the Rayleigh fractionation process in purification,the difference inδ137/134Ba between the initial and final stages did not exceed0.060‰(or 0.045‰)when leaching the standard sample with HCl or HNO_(3),which is equal to or less than the accuracy of Ba isotopic analysis.At a common yield of89.75%,Ba isotopic fractionation induced by incomplete recovery was 0.015‰for HCl(or 0.011‰for HNO_(3)).Finally,if the influence of an incomplete recovery on theδ137/134Ba determination needs to be ignored,the recovery is suggested to be not less than 67%for HCl(or 46%for HNO_(3)).

PREPARATION AND CHARACTERIZATION OF ION EXCHANGE MEMBRANES BASED ON POLYVINYLIDENE FLUORIDE

A new ion exchange membrane based on polyvinylidene fluoride (PVDF) and sulfonated poly(styrene-divinylbenzene) was prepared by in-situ polymerization. The incorporation of sulfonic groups into the polyvinylidene fluoride composite membrane was confirmed by infrared spectroscopy (IR), ion exchange capacity (IEC) and energy dispersive X-ray analysis (EDAX). Area resistance, IEC and water uptake of the treated membrane were evaluated. When 20% of the crosslinked membrane was sulfonated at 80degreesC for 22 h, the PVDF ion exchange membrane can attain 0.8 Omega . cm(2) area resistance in NaCl aqueous solution at 25degreesC, IEC is as high as 2.43 millimoles per grain of the wet membrane. The hydrophilicity of PVDF membrane is also significantly improved after treatment. When 60% of crosslinked membrane was sulfonated at 80degreesC for 6 h, water uptake of the treated membrane can attain 64.7%.

Effects of Polar Organic Solvent on Separation of Y(edta)^-/Nd(edta)^- Complexes on Polyacrylic Anion Exchangers

The use of polar organic solvents for the separations of rare earth elements (Ⅲ) is effective especially for their extensive separations despite the solubility limitations. The study shows that polyacrylate anion exchangers, particularly the weakly basic, gel anion exchanger Amberlite IRA 68, can be applied to the separation of rare earth complexes with EDTA in H_2O-methanol and H_2O-ethanol systems. In most cases the determined distribution coefficients of Ln^(3+) complexes with EDTA in mixed media like water-methanol on polyacrylate anion exchangers are larger than those in pure water (media.)

Ion Exchange Reaction between Polycrystalline Na β″-Alumina and LaCl_3

1.IntroductionDunn and Farrington[1]found that theNa ion in Naβ″-alumina single crystal canbe exchanged completely or partially withGd;,Nd;,Eu;,Yb;,Sm;,Tb;,Dy;,Bi;and Pr;ions,but no reports havebeen published about the ion exchange reac-tion between La3+ and Naβ″-alumina.If anion exchanged polycrystalline β″-alumina isavailable and its ionic conductivity is highenough to be applied as a solid electrolyte inthe galvanic cell,it can be used in various

Kinetic Process and Conductivity of Ag^+ Ion Exchange for Polycrystalline Na-β"-Al_2O_3

This paper reports the kinetic process of Ag ion exchange for the polycrystalline Na-β'-Al2O3.The interdiffusion coefficients in the process of Ag+ and Na+ ion exchange have been calculated with an 'one dimensional double side diffusion model'. Microstructures of the samples were observed and analysed by XRD, EMPA, SEM. The results of the conductivity measurements for samples with Na+, Ag+ and Na+-Ag+ mobile ions are presented and explained

STUDY ON THE ELECTROCHEMICAL BEHAVIOR OF ION EXCHANGE MEMBRANE IN PREPARING POTASSIUM CARBONATE

This investigation describes the one step preparation of potassium carbonate by electrolysis of potas-sium chloride solution in electrolyzers with various Nation membranes.Potassium bicarbonate solution wasfed to the cathode compartment,where it was converted into carbonate by reaction with the hydroxideformed at cathode.Because of the low OH^- concentration in the cathode compartment,the back migrationof OH^- through the membrane was almost negligible,resulting in a higher current efficiency,say 90% or more.In this study,electroconductivity,mass transfer,current efficiency and cell voltage were measured.Thefeasibility of the process was discussed and the optimal conditions examined.

Reactive ion exchange synthesis of high pure nano-CeO_2

This paper presents a reactive ion exchange synthesis method of nano-CeO2 with positive cerium preexchanged ion exchange resin as precursor and ( NH4) 2CO3 as precipitant. The resultant precipitate was dried at 100 ℃ for 12 h and then was calcined at 500 K in air. The effects of ion exchange temperature and reaction time on the diameter of CeO2 particle were discussed. The TEM images show that the samples prepared with one step reactive ion exchange method are composed of nano-club with the length about 300 nm.