Adsorption behaviors of strontium using macroporous silica based hexagonal tungsten oxide

A novel macroporous silica-based hexagonal tungsten oxide (h-WO₃/SiO₂) with exchangeable sodium cations located in hexagonal tunnel structure was synthesized by a facile hydrothermal treatment of sodium tungstate dihydrate with 1 mol/L HCl solution. Utilization of the h-WO₃/SiO₂ adsorbent to remove aqueous strontium was investigated under the condition of various pH values, contact time, the initial concentration of metal ions, salt ion concentration, and coexisting ions. According to the experimental data, Sr²⁺ adsorption equilibrium was achieved within 15 min in acidic solution, and the maximum removal capacity of Sr²⁺ occurred at pH 4. The kinetic adsorption of Sr²⁺ on h-WO₃/SiO₂ was controlled by pseudo second-order model, and the saturated adsorption of Sr²⁺ on h-WO₃/SiO₂ was better described by Langmuir and Redlich-Peterson isotherm models compared with the Freundlich isotherm model. The distribution coefficient of Sr²⁺ was more than 2000 cm³/g in the presence of Ca²⁺, Mg²⁺, La³⁺, and Eu³⁺, indicating that the h-WO₃/SiO₂ showed excellent selectivity towards Sr²⁺ in pH 4.     

Comparative Adsorption of Lead(II) on Flake and Bead‐Types of Chitosan

The adsorption of Pb(II) ions from aqueous solutions by chitosan flakes and beads was studied. The chitosan beads were prepared by casting an acidic chitosan solution into alkaline solution. Experiments were carried out as a function of pH, agitation period and initial concentration of Pb²⁺ ions. The uptake of Pb²⁺ ions from aqueous solution was determined from changes in concentration as measured by atomic absorption spectroscopy. The maximum uptake of Pb²⁺ ions on chitosan beads was greater than that on chitosan flakes. Adsorption isothermal data could be interpreted by the Langmuir equation. The experimental data of the adsorption equilibrium from Pb²⁺ ion solutions correlated well with the Langmuir isotherm equation. SEM analyses were also conducted for visual examination of the chitosan flakes and beads. Physical properties including surface area and average pore diameter were characterized by N₂ adsorption experiment.     

Factors affecting the sorption behavior of Cs<Superscript>+</Superscript> and Sr<Superscript>2+</Superscript> using biosorbent material

In this study, saw dust has been used as precursor for production of low cost activated carbon using potassium hydroxide (KOH) and steam activation technique. The activated carbon was used to remove Cs⁺ and Sr²⁺ ions from aqueous solutions by batch operation, and the extent of adsorption was investigated as a function of solution pH, temperature, shaking time, and initial concentration. The influence of interfering ions was also investigated. The removal of metal ions was pH dependent and the adsorption capacity reaches its maximum 43% and 61.5% at pH 5.0 and 6.0 for Cs⁺ and Sr²⁺ ions, respectively. Thermodynamic studies showed different behaviours where an endothermic, non-spontaneous process was shown for Cs⁺ while an exothermic, spontaneous process was obtained for Sr²⁺. The kinetic data of both ions was described well by pseudo-second order rate equation. The two equilibrium models (Langmuir and Freundlich) have been also applied. Desorption studies indicated that HCl was the most effective desorbing eluent. The investigated adsorbent showed good results towards cesium and strontium removal from aqueous media that could be a promising method due to its low-cost and good efficiency.     

An adsorption study of Sr2+ from saline sources by coconut shell charcoal

The adsorption potential of charcoal for the removal of heavy metal ions is well documented in the literature. However, its exploration for uptake of technologically valuable metal ions such as Sr²⁺ is poorly known. In this work, the batch adsorption study of Sr²⁺ ion from aqueous solution as well as from saline matrix (>3% of NaCl) onto charcoal has been carried out. The experiments were conducted with two charcoals, i.e., our prepared charcoal (coconut shell charcoal) and commercial charcoal. Strontium adsorption has been investigated as a function of its initial concentration, contact time, and varied mass of adsorbent. Equilibrium adsorption data were evaluated for Langmuir and Freundlich isotherm models. The adsorption capacities (mg/g) of Sr²⁺ present in the salt matrix onto coconut shell charcoal and commercial charcoal was found to be 18.4 and 22.2, respectively. Uptake of Sr²⁺ from subsoil brine onto coconut shell charcoal has been successfully demonstrated in this work.     

Synthetic calcium aluminosilicates and their sorption properties with respect to Sr<Superscript>2+</Superscript> ions

Sorption characteristics of synthetic calcium aluminosilicates (CAS) obtained in the multicomponent CaCl₂–AlCl₃–KOH–SiO₂–H₂O system are presented. The isotherms of Sr²⁺ sorption on CAS from aqueous solutions containing no additional salts were measured for Sr²⁺ concentration from 0.5 to 11.1 mmol/L and solid to liquid phase ratio S: L = 1: 100. The maximum sorption capacity of synthetic CAS was determined, the phase distribution constants of Sr²⁺ ions at different S: L ratios were found. The recoveries of Sr²⁺ ions from solutions containing 0.01 mol/L Ca(NO₃)₂ and from a solution simulating water of the Mayak plant sewage pond No. 11 were determined.     

Selective removal of Cd(II), As(III), Pb(II) and Cr(III) ions from water resources using novel 2-anthracene ammonium-based magnetic ionic liquids

Facile synthesis of two 2-anthracene ammonium-based magnetic ionic liquids (MILs), 2-anthracene ammonium tetrachloroferrate (III) ([2A-A]FeCl₄) and 2-anthracene ammonium trichlorocobaltate (II) ([2A-A]CoCl₃) was performed by protonation of 2-aminoanthracene, followed complexation with FeCl₃/CoCl₂. The MILs were tested in the adsorptive removal of Cd²⁺, As³⁺, Pb²⁺ and Cr³⁺ from water sources. Upon treatment with 10 mg dosage of MILs in 10 mL aqueous solution of 50 ppm each of Cd²⁺, As³⁺, Pb²⁺ and Cr³⁺, adsorption capacity (mg/g) in the range of 5.73–55.5 and 23.6–56.8 for [2A-A]FeCl₄ and [2A-A]CoCl₃ respectively were recorded. Thus, the optimization, kinetic and isotherms studies were conducted using the [2A-A]CoCl₃ adsorbent. The [2A-A]CoCl₃ was more effective in pH 7–9, and equilibrium adsorption was achieved after 60 min contact time. The adsorption process proceeded via the Pseudo-second order pathway and the Langmuir isotherm model is the best fit for the adsorption process (with q_max = 227 – 357 mg/g) of all the targeted metal ions. The [2A-A]CoCl₃ adsorbent demonstrated practicality with large distribution and selectivity coefficients of the targeted ions, and up to six times regeneration.     

Preparation of core-shell magnetic Fe3O4@SiO2-dithiocarbamate nanoparticle and its application for the Ni2+, Cu2+ removal

A typical superparamagnetic nanoparticles-based dithiocarbamate absorbent (Fe₃O₄@SiO₂-DTC) with core-shell structure was applied for aqueous solution heavy metal ions Ni²⁺, Cu²⁺ removal.     

Effect of Sr2+ doping on the luminescence properties of YVO4:Eu3+,Sr2+ particles prepared by a solvothermal method

Well-dispersed Eu³⁺ and Sr²⁺ co-doped YVO₄ luminescent particles (YVO₄:Eu³⁺,Sr²⁺) on the submicron scale were prepared by a facile solvothermal method at low temperature. The effect of Sr²⁺ doping on the luminescence of YVO₄:Eu³⁺,Sr²⁺ particles was investigated by fixing the Eu³⁺ doping concentration at 7 mol%. It was found that the luminescence intensity of the as-prepared YVO₄:Eu³⁺,Sr²⁺ particles increased with the Sr²⁺ doping concentration x to reach a two-fold enhancement when x = 5 %, and then decreased for higher x. We also investigated the effect of thermal annealing on the luminescence properties of the YVO₄:Eu³⁺ and YVO₄:Eu³⁺,Sr²⁺ particles. A remarkable enhancement in their luminescence properties was observed after annealing at 900 °C in air for 30 min. It was showed that the annealed YVO₄:Eu³⁺,Sr²⁺ particles exhibited a two-fold stronger emission than the annealed YVO₄:Eu³⁺. This work indicates that Sr²⁺ doping is beneficial to the luminescence enhancement for both the as-prepared and annealed YVO₄:Eu³⁺,Sr²⁺ particles.     

Isotope exchange of strontium and molybdate ions in strontium polymolybdates

The heterogeneous isotopic exchange reactions in strontium polymolybdates of Sr²⁺ and MoO₄ ^2- ions in the strontium nitrate and sodium molybdate solutions have been studied using ⁹⁰Sr and ⁹⁹Mo as tracers. Electrometric methods have been used to study the compositions of strontium molybdates obtained by adding strontium chloride to a progressively acidified solution of sodium molybdate. It has been found that the exchange fraction increases with increasing chain length of strontium polymolybdate. The exchange equilibrium constant (K _ex) has been calculated between 298 and 348 K as well as DG°, DH° and DS°. The results indicate that Sr²⁺ cations have a much higher affinity for exchangers than MoO₄ ^2- anions. By fitting the data to the Dubinin-Radushkevich (D-R) isotherm it has been shown that the exchange capacity (X _m ) for both ions is affected by the ion adsorption process at low temperatures and by the ion exchange process at high temperatures. At high concentrations, the recrystallization process contributes to on the cation exchange but is ineffective on the anion exchange mechanism.     

Tailored functionalized polymer nanoparticles using gamma radiation for selected adsorption of barium and strontium in oilfield wastewater

To improve oil recovery from oilfield wells mineral scales derived by insoluble BaSO₄ and SrSO₄ salts during oil extraction should be diminished. In this work, adsorption selectivity of Barium (Ba²⁺) and Strontium (Sr²⁺) ions associated with saline formation waters was examined for the first time using nano-sized bi-functional polymer blend synthesized by Cobalt-60 (⁶⁰Co) γ-rays, as green technology. A bifunctional polymer formed from poly(acrylonitrile)/(styrene-butadiene rubber) homogenous blend is functionalized by -SO₃H and -COOH terminal groups (termed as SASB). Those functional groups were selected based on systematic calcium (Ca²⁺) ions adsorption studies of carboxylate containing molecules. Main and binary interactive effects of solution pH (3–9), adsorbents dose (1-3 g/L), total dissolved salts (TDS, up to 30 g/L), initial Ba²⁺ and Sr²⁺ concentrations (10-500 mg/L) and temperature (20–50 ^oC) on the adsorption selectivity were examined and optimized using Plackett-Burman factorial design (PBD) combined with multiple regression analysis. The regression statistics revealed the significance of quadratic polynomial model to optimize interactive sorption conditions from salty waters with high accuracy level ($R^2$≈ 0.99) rather than linear and two-way interactive models at 95% confidence level. Interestingly finding, the regression and experimental data proved that the presence of up to 10 g/L TDS from alkali metal ions had a significant effect on the enhancement sorption capacity of Ba²⁺ and Sr²⁺ when using the prepared sorbent. The SASB adsorbent showed higher sorption selectivity with maximum equilibrium capacity ($q_{\mathit{mg}/g}$) of 175.3 mg Ba⁺² and 210.5 mg Sr⁺² per each gram sorbent used in kinetic study. Adsorption kinetics of Ba²⁺ and Sr²⁺ sorption by both adsorbents obey pseudo-first and pseudo-second order kinetics, respectively. In sum, the adsorptive power of SASB sorbent is found to be in reverse order of the electronegativity and the hydration radii of the metal ions.     

Adsorption of strontium ions from aqueous solution using hydrous,amorphous MnO2–ZrO2 composite: a new inorganic ion exchanger

Hydrous, amorphous MnO₂–ZrO₂ composite was prepared as a new inorganic composite material under various conditions for removal of Sr²⁺ ion from aqueous solutions. The physico-chemical characterization was carried out by Fourier transform infrared spectroscopy, X-ray powder diffraction, scanning electron microscopy and thermogravimetry. The maximum sorption capacity for synthesized composite was evaluated as 1.5 meq/g sorbent and batch experiments were carried out as a function of contact time, aqueous phase pH, temperature and initial metal ions concentration of adsorptive solution. The results indicated that under optimal conditions, Sr²⁺ ions could be efficiently removed using MnO₂–ZrO₂ composite from aqueous solutions when pH > 5. The equilibrium isotherms were determined and the sorption data were successfully modeled using Langmuir model. Kinetics of the process was studied by considering a pseudo second-order model. This model predicted chemisorption as the adsorption mechanism. The results of thermodynamic investigation reveal that the adsorption process of the studied ion is entropy driven.     

Preparation and ion-exchange properties of zirconium tungstoarsenate

A new inorganic ion-exchanger, zirconium tugnstoarsenate, has been synthesized which has been characterized by chemical analysis, thermogravimetry, X-ray and infrared spectroscopy. The ion exchanger has been found to be stable in acids and neutral salt solutions. The K_d values for 30 metal ions have been determined at pH 3–4 which show that the exchanger has high affinity for UO ₂ ²⁺ , ZrO²⁺, Cs⁺ and Tl⁺ ions. The variation of K_d for a number of metal ions as a function of concentration of nitric acid and ammonium nitrate has been investigated to elucidate the probable exchange mechanism and to work out conditions for elution. Some binary separations, viz. Sr²⁺−Cs⁺, Sr²⁺−Rb⁺, Sr²⁺−Y³⁺, Fe³⁺−Al³⁺, Fe³⁺−Zn²⁺ and Zn²⁺−Hg²⁺ in trace amounts have been carried out on the column of the exchanger which demonstrate the utility of the exchanger in radionalytical and analytical chemistry.     

Synthesis and characterization of tin(IV) antimonate and study of its ion-exchange equilibria

Tin(IV) antimonate with different Sb/Sn molar ratios has been prepared. The characterization of the product materials was carried out using X-ray diffraction pattern, themal analysis and infrared spectra. The saturation capacities of sodium and cesium were found to increase with Sb/Sn molar ratios. TheK _d values on thermal treatment of tin(IV) antimonate, as a cation exchanger, have been measured for some heavy metal ions in the temperature range of 50–400 °C. The maximum adsorption of 10^–4M of the metal ions studied was obtained at 400 °C. The selectivity sequence was Eu³⁺>Co²⁺>Sr²⁺>Cs⁺ for the sample heated up to 400 °C. No adsorption was observed on the sample heated at 700 °C because of the formation of SnO₂ and Sb₆O₁₃.     

Microstructure,dielectric and piezoelectric properties of (Pb1−xSrx)Nb1.96Ti0.05O6 ceramics

(Pb_1−xSr_x)Nb_1.96Ti_0.05O₆ with 2 wt% excess PbO (x = 0, 0.02, 0.04, 0.06, 0.08) piezoelectric ceramics with high Curie temperature were fabricated via the conventional solid state reaction method. Effects of Sr²⁺ amount on crystallite structure, microstructure, dielectric and piezoelectric properties were studied. The substitution of Sr²⁺ ions for Pb²⁺ ions is effective to lower sintering temperatures. X-ray diffraction patterns indicate that all ceramics form the single orthorhombic ferroelectric phase. The doping of Sr²⁺ ions facilitates improving densification of the ceramics. Grain size and lattice parameters of the ceramics vary with the change of the Sr²⁺ contents. Both Curie temperature and maximum dielectric constant change with increasing the Sr²⁺ amounts. The dielectric constant data were also studied using the Curie–Weiss law and modified Curie–Weiss law. The ceramic with x = 0.04 possesses excellent piezoelectric and dielectric properties, presenting a high potential to be used in high-temperature applications as piezoelectric transducers.     

Surface characterization and thermodynamics of adsorption of Sr2+, Ce3+, Sm3+, Gd3+, Th4+, UO 2 2+ on activated charcoal from aqueous solution

Surface parameters of the activated charcoal were measured using precise instrumental techniques for dehydration, carbon content, trace metals impurities, anions, bulk, tap and true densities, surface area, pore volume, porosity and average particle diameter. The adsorption of Sr²⁺, Ce³⁺, Sm³⁺, Gd³⁺, Th⁴⁺ and UO ₂ ²⁺ ions on activated charcoal from aqueous solution was studied as a function of temperature. Thermodynamic parameters such as HH ⁰ and S ⁰ were calculated from the slopes and intercepts of the linear variation of lnK ₁ vs. 1/T, whereK ₃ is obtained from Langmuir equation. The results show endothermic heats of adsorption, but negative free energy values indicate that the adsorption process of metal ions on activated charcoal is favored at high temperature. The value of isosteric heat of adsorption, calculated from the Clausius-Clapeyron equation, shows that the surface of the activated charcoal is heterogeneous with respect to activity. A wavelength dispersive x-ray fluorescence spectrometer was used for measuring the concentration of metal ions.     

Biosorption of strontium from aqueous solutions onto spent coffee grounds

A set of experiments was carried out to evaluate the strontium uptake potential of spent coffee grounds (SCG) by batch tests in aqueous medium. Adsorption of Sr²⁺ as a function of contact time and adsorbent dose, pH, particles size, agitation speed, temperature and co-ions presence was investigated. Obtained results revealed that the maximum adsorption took place at pH range of 5–8 and temperature values between 283 and 333 K. Particles size effect was not very significant and agitation speed influenced on the equilibrium time. Competitive adsorption experiments allowed us to classify the negative effect on the Sr²⁺ uptake according to this order Al³⁺ ? Co²⁺ > Mg²⁺ > Ca²⁺ ? Na⁺ > K⁺ > Cs⁺. Kinetic study indicated that the Sr²⁺ uptake was fast and it was well fitted by the pseudo second order reaction model. Adsorption isotherm was well interpreted by Langmuir model. The maximum adsorption capacity was found to be 69.01 mg g^?1 at pH 7, 293 K, particles sizes = 200–400 μm and agitation speed 250 rpm. The thermodynamic study revealed that the process was spontaneous (ΔG ⁰ < 0), exothermic (ΔH ⁰ < 0) with a raised affinity for Sr²⁺ (ΔG ⁰ < 0, ΔS ⁰ > 0) and occurred by physical adsorption (E _a = 8.37 kJ mol^?1). FTIR analysis showed carboxylic acid and amino group presence on SCG surface playing a vital role in Sr²⁺ biosorption.     

Batch and continuous fixed-bed column adsorption of Cs+ and Sr2+ onto montmorillonite–iron oxide composite: Comparative and competitive study

A montmorillonite–iron oxide composite (MIOC) was prepared to assess its effectiveness in the removal of Cs⁺ and Sr²⁺ from aqueous solution. A comparative and competitive adsorption study was conducted in single and binary systems. Used materials have been characterized by X-ray diffraction (XRD) and Infrared spectroscopy. Adsorption of Cs⁺ and Sr²⁺ as a function of contact time and pH was investigated, adsorption data of single metal solutions were well fitted to the Freundlich–Langmuir isotherm models. Equilibrium isotherms for the binary removal of Cs⁺ and Sr²⁺ by MIOC have been analyzed by using non modified and extended Langmuir models with a satisfactory R ² values. Neutral solution pH was found to be favorable for both single and binary systems. The adsorption model analysis revealed that MIOC was more selective for Sr than Cs. The maximum adsorption capacities for individual Cs⁺ and Sr²⁺ solutions were 52.6 and 55.5 mg g^?1, respectively. While the maximum uptakes in the binary system were 41.6 and 47.6 mg g^?1 for Cs⁺ and Sr²⁺, respectively. Column adsorption experiments were carried out at room temperature under the effect of various operating parameters such as bed depth, initial cation concentration and flow rate, Breakthrough curves were well fitted to the Thomas model. Desorption experiments were also conducted to assess the possibility for the reuse of adsorbent and the recovery of cations.     

Adsorption of some hazardous radionuclides on cerium (IV) antimonate

Cerium(IV) antimonate was prepared by dropwise addition of 0.6M antimony pentachloride and 0.6M cerium ammonium nitrate solutions by a molar ratio of Ce/Sb 0.75. Exchange isotherms for H⁺/Co²⁺, H⁺/Cs⁺, H⁺/Zn²⁺, H⁺/Sr²⁺ and H⁺/Eu³⁺ were determined at 25, 40 and 60°C. Besides, it was proved that europium is physically adsorped, while zinc, strontium, cobalt and cesium are chemically adsorbed. Moreover, the heat of adsorption of zinc, strontium, cobalt and cesium on cerium (IV) antimonate was calculated and indicated that cerium(IV) antimonate is of endothermic behavior towards these ions. Also the distribution coefficients of these ions were determined and it was found that the selectivity is in the order: Eu³⁺>Sr²⁺>Cs⁺>Na⁺.     

The state of Cu2+ ions in concentrated aqueous ammonia solutions of copper nitrate

Stabilization of Cu²⁺ ions in concentrated aqueous ammonia solutions of copper nitrate in a wide range of ammonium ion concentrations has been studied by EPR and electronic absorption spectroscopy. Three types of Cu²⁺ associates with different types of orbital ordering have been identified. The ammonium ion concentration in a solution has a decisive effect on the type of orbital ordering of Cu²⁺ ions in associates. In all cases, Cu²⁺ ordering in associates is caused by the existence of bridging OH groups in the axial and equatorial positions of [Cu(NH₃) _n (H₂O)_{6 ? n} ]²⁺ complexes (n < 6). At a high concentration of ammonium ions, weakly bound associates of tetramminecopper with the $d_{x^2 - y^2 }$ ground state are formed. In solutions with low ammonium concentrations, bulky associates with the $d_{y^2 }$ and $d_{x^2 - z^2 }$ ground states and associates of Cu²⁺ ions with the $d_{x^2 - y^2 }$ ground state with hydroxyl groups in the equatorial plane and axial water molecules are formed.