Abstract
An organic–inorganic ion exchanger namely sodium titanosilicate-polyacrylonitrile (STS-PAN) composite was synthesized and used for the adsorption of 137Cs from a typical aqueous solution. The physicochemical behavior of the ion exchanger was specified with different techniques including Fourier Transform Infrared Spectroscopy (FT-IR), X-ray powder diffraction (XRD), specific surface analysis (BET), thermogravimetry-differential scanning calorimetry (TG-DSC), scanning election microscopy (SEM), X-Ray Fluorescence spectroscopy (XRF) and CHN elemental analysis. The thermal and gamma irradiation stability of the synthesized ion exchanger was investigated. It was observed that the ion exchanger is stable up to 275 °C and against gamma irradiation up to 200 KGy. The effects of pH, contact time, ambient temperature, and presence of various cations on adsorption rate of STS-PAN were also studied and the optimum conditions obtained. In addition, thermodynamic parameters were evaluated during the adsorption. The values of the enthalpy and the Gibbs free energy suggest an endothermic and spontaneous process. Adsorption isotherm in batch experiment showed that the sorption data were successfully fitted with Langmuir model. Finally the adsorption dynamic capacity of the synthesized composite in a columnar experiment as well as its elution was evaluated. The complete breakthrough curve was generated at a feed rate of 15 bed volume per hour and sorbent capacities were obtained at 5 and 100% breakthrough.
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Introduction
There are a number of liquid processes and waste streams at nuclear facilities that require treatment and/or the removal of radioactive contaminants. Cesium and strontium are the most abundant radionuclides in nuclear fission products that are routinely or accidentally released. They have relatively long half-life of about 30 years and are considered as hazardous elements for the environment. Ion exchange technique has become one of the most commonly used treatment methods for such aqueous streams due to its simplicity, selectivity and efficiency. A wide range of materials having different chemical and physical properties, which can be naturally occurring or synthetic, is available for this technique [1–11].
Several inorganic ion exchangers such as zeolites, sodium titanates, silicotitanates, metal oxides and hexacyanoferrates are in use in nuclear sites for the treatment of nuclear wastes. However, the slow mass-transfer rate in column operation has been the impeding factor for extensive applications. On the other hand, the application of organic ion exchange resins to the wastes treatment has been decreased because they possibly release the radionuclides by decomposition of organic binding matrix when disposed underground. These reasons have recently expedited the study on the preparation and the application of organic–inorganic composite ion exchangers for the treatment of various radioactive and industrial waste waters. In composite ion exchanger, inorganic materials are active components to which all the radionuclides are bound and organic materials are simply inert binders. Therefore, contrary to the organic ion exchange resins, even in the case of decomposition of organic binding matrix, no radionuclides are released [12, 13].
Polyacrylonitrile (PAN) is reportedly one of the most favorable organic binders, due to its characteristic features such as excellent pelletizing property, good solubility for organic solvents, strong adhesive forces with inorganic materials and chemical stability [14]. PAN beads are highly porous and can accommodate very high loadings of ion exchange material (5–95%) into the PAN matrix. These highly porous PAN beads exhibit a number of advantages over other granular sorbents. These advantages include significantly improved kinetics and sorbent capacity owing to the increased availability of the sorbent material, easy modification of physico-chemical properties (hydrophilicity, porosity, mechanical strength) and simplified production. Several authors published papers on the use of PAN as a binding polymer for granulating different inorganic cation exchangers [15–18]. Todd et al. used PAN-AMP containing ammonium molybdophosphate granulated with PAN to study the uptake of cesium from concentrated acidic wastes [19]. Also Zn and Cu hexacyanocobaltates was supported on PAN and used successfully for removal of the radioactive cesium from different aqueous solutions [20].
This paper presents the preparative conditions, adsorption properties and analytical applications of sodium titanosilicate-polyacrylonitrile polymeric-inorganic composite material used as a cation exchanger for removal of 137Cs from aqueous solutions.
Experimental
Reagents and apparatus
All the reagents and chemical used were of analytical grade obtained from Merck, Fluka, and Aldrich. Radioactive tracer 137Cs was supplied by Nuclear Science and technology Research Institute of Iran and subsequently used to label the Cs+ solutions of desired concentrations prepared by dilution of 0.1 mol/L Cs+ stock solution.
The infrared spectra was recorded using a Brucker-Vector 22 spectrophotometer; X-ray powder diffractometry was carried out using an 1800 PW Philips diffractometer with CuKα beam in order to determine the structure of the adsorbers. The X-ray source was a rotating anode operating at 40 kV and 30 mA with a copper target and the data were collected between 5 and 70° in 2θ; Brunauer–Emmett–Teller (BET) specific surface area was determined through nitrogen adsorption isotherms using Quantachrome NOVA 2200e system; Scanning electron microscope (SEM) imaging was performed by means of a Philips XL30; thermogravimetry-differential scanning calorimetry (TG-DSC) were carried out on heating the sample up to 800 °C at a heating rate of 10 °C/min in the Argon atmosphere using a DuPont model 951; carbon, hydrogen and nitrogen contents of the composite was determined using an Elementar-Vario ELIII, CHN elemental analyzer; the amount of Na+, K+, Ca2+ and Mg2+ cations was measured by a Perkin Elmer atomic absorption spectrometer (AAS) model 843; The X-Ray Fluorescence Unit (Oxford ED 2000) which is used to determine the amount of titanium and silicon, the radioactivity was counted using a high purity germanium detector gamma spectrometer Ortec model GMX-15185-5 and finally the pH measurement were made with a Schott pH-meter model CG841.
Preparation of composite adsorbent
For sodium titanosilicate preparation, 39 mL of 6 mol/L NaOH solution was added to 6.8 g of tetraethyl orthotitanate 97% and 5.0 g of tetraethyl orthosilicate 99%. The synthesis was carried out under hydrothermal conditions at temperature 150 °C for 5 days. The precipitate was filtered and washed with distilled water then ethanol. The solid was then dried at 100 °C and sieved to size of 224–400 μm.
For composite beads preparation; the weighed amount of sodium titanosilicate powder was mixed with the solvent dimethylsulfoxide (DMSO) and a few drops of Tween-80 surfactant and stirred at 50 °C for 3 h. Then, 2.4 g of polyacrylonitrile powder were added to this solution with stirring at 50 °C for 4 h to obtain homogeneous solution of the composite dope. The dissolved air in the dope was removed by vacuum pump, and the air-free composite dope as described in previous study, was passed through inside the dual nozzle while the compressed air was ejected through the outside annulus of the dual nozzle to adjust the size of the composite beads [21]. The ejected composite beads were then dropped in distilled water, which was used as a gelation agent. Finally, the beads were washed using demineralized water and dried at 50 °C. The bead sizes were varied in the range of 2–3 mm with the air pressure variation.
Experimental procedure
The adsorption experiments have been studied by batch technique. 0.1 g of the prepared composite ion exchanger and 10 mL of the labeled 10−4 mol/L cesium solution of desired pH were shaken with uniform speed using a thermostated shaker bath. pH of the adsorptive solutions was adjusted with the suitable quantity of NaOH and HCl, monitored with a digital pH meter. All experiments were carried out at 25 °C except for the temperature dependence studies where temperature varied from 25–65 °C. Before adding the adsorbent, an aliquot of the bulk solution was withdrawn for the measurement of the initial radioactivity. For the evaluations of distribution coefficient (K d) of cesium as a function of contact time, from 5 to 120 min time intervals were applied. At the end of each time interval, the solution was filtered for phase separation and the radioactivity of supernatant solutions was measured, then K d for adsorbed cesium on the composite was determined from the following equation:
where R o and R e are radioactivity in the initial and equilibrium stages, V the solution volume (mL) and m is the mass of sorbent (g).
Also the same experimental conditions were applied in order to investigate the influence of Na+, K+, Ca2+ and Mg2+ cations on the distribution coefficient (K d) of cesium.
The sorption isotherm experiments were conducted at the temperature of 25 °C and pH 6.0 (±0.1) by batch sorption procedure. 0.1 g of adsorbent was mixed with 10 mL samples of different initial concentration of Cs+ solution and were shaken in order an equilibrium could be achieved.
Results and discussion
Synthesized composit characteristics
Figure 1 depicts XRD patterns of three synthesized materials: (a) Polyacrylonitrile, (b) STS, and (c) STS-PAN. The analysis of X-ray patterns revealed that the XRD data corresponding to the synthetic STS agreed well with previously reported papers [22, 23]. It was also observed that no diffraction peaks can be seen in the pattern of polyacrylonitrile which indicates an amorphous structure but the 2θ values at the peak points of STS-PAN are the same as those in STS, and hence their crystalline structure is very similar. Using the above facts, it was determined that STS-PAN composition has been accurately synthesized.
The IR spectrum of STS-PAN composite is recorded in Fig. 2. The broad band in the region of 2800–3650 cm−1 is due to interstitial water and hydroxyl groups and the sharp peak at 1650 cm−1 corresponds to the bending vibration of water molecules. Absorption peak at 495 cm−1 can be assigned to the bending vibration of Ti–O. The spectrum of the sample shows the characteristic band for –CH2 at 1465 cm−1. The band at 950 cm−1 is assigned to the Si–O–Ti bond stretching vibration in exchanger structure. The bands in the 750 cm−1 region are due to the Si–O vibration in the synthesized composite. Finally, the sharp peak in 2250 cm−1 can be assigned to the nitrile group.
The nitrogen adsorption–desorption studies showed that the BET surface area of sodium titanosilicate—polyacrylonitrile composite is 96.66 m2/g.
Scanning electron microscope (SEM) imaging of the prepared STS-PAN composite bead is shown in Fig. 3. To take SEM photographs, electrons are usually accelerated within a range of 1–30 keV. This image indicates that the pore size of the inner part of the particles was larger than that near the surface. The kinetic of sorption on these adsorber beads must be very fast, since the STS powder which is the active material for adsorption, is found to be dispersed throughout the binding matrix. In other word, this image indicates the structure of synthesized STS is tunnel-shaped with a high adsorption level.
Using a CHN unit, elements of carbon, hydrogen and nitrogen contained in the composite were measured, and XRF spectroscopy was used to determine the amount of titanium and silicon. The results achieved are shown in Table 1.
The TGA-DSC thermal analysis of STS-PAN composite is shown in Fig. 4 which shows decomposition steps. This Figure demonstrates that weight reduction up to 275 °C occurs due to elimination of free water molecules; and above this temperature (275–370 °C); structural collapse of polymers contained in the composite will cause reduction of adsorbent weight. Finally, in temperatures between 370–655 °C, weight reduction is due to release of space lattice water molecules outward and emission of hydrogen cyanide (HCN) gas from the synthesized compound. Therefore, sodium titanosilicate-polyacrylonitrile is stable up to 275 °C.
Stability of STS-PAN against gamma irradiation
Through assessment of IR spectrum of STS-PAN composite, probable variations in the exchanger structure as a result of gamma rays can be predicted. IR spectra of the sample prior to gamma irradiation (100 and 200 KGy doses) and after that were compared.
As it can be seen in Fig. 5, no change is observed among IR spectra of all three samples (a-unpredicted by gamma, b- gamma-irradiated up to 100 KGy, c-gamma-irradiated up to 200 KGy); in the other words, the synthesized composite will be stable against gamma irradiation up to 200 KGy under which no change occurs through the composite’s structure.
Adsorption characteristics
Effect of contact time
Pursuant to the assessment of factors having impact on cesium adsorption, the influence of contact time between cesium solution and STS-PAN on distribution coefficient of cesium was investigated. As it can be seen in Fig. 6, the adsorption rate soars with time increase, and equilibrium is maintained between two phases after about 130 min. In the subsequent experiments, the contact time of 130 min was selected for sorption equilibration of Cs+ on STS-PAN.
Effect of solution initial pH
The effect of pH on the sorption of Cs+ ions from aqueous solutions using the prepared composite material was investigated over the pH range of 1.0–9.0 (Fig. 7). It was observed that the distribution coefficient of cesium continuously increases with increasing pH and the optimum pH value at which the maximum adsorption could be achieved was 6.0. Low distribution coefficient in acidic environments can be attributed to competition of H+ cations with cesium ions for the exchange sites in the adsorbent.
Effect of other cations
Change of distribution coefficient values of Cs+ cation along with the tracer was evaluated in the presence of Na+, K+, Ca2+ and Mg2+ cations at 10−4 mol/L concentration added in the form of their nitrates at 298 K. The results (Table 2) indicate that the distribution coefficient of cesium has decreased in the presence of added cations.
Effect of solution temperature
The effect of medium temperature of distribution coefficient with regard to Cs+ cation was examined, while other parameters were kept constant (adsorptive concentration for Cs+ 10−4 mol/L and pH 6.0).
The results obtained in Table 3 reveal that rising of the medium temperature from 298 K to 338 K (from 25 °C to 65 °C), in steps of 10 K (10 °C), brings about positive impact on the magnitude of distribution coefficient. As temperature goes up, the required energy for precipitation of hydrated cations layers is provided, and it also leads to enhancement of cations motion existing in exchanging network and facilitates the interaction. Therefore, the above exchanging process is endothermic.
Process thermodynamic parameters
Variation of standard thermodynamic parameters during the adsorption process was evaluated using the following equations [24]:
where ∆H°, ∆S° and T are the standard enthalpy, standard entropy, and temperature in Kelvin, respectively, and R is the gas constant. Considering the above equation and by drawing Ln K d diagram in terms of 1/T, values of ∆H° and ∆S° are determined. The values of enthalpy and entropy can be obtained from the slope and intercept of linear variation of ln K d with reciprocal temperature (Fig. 8). The standard Gibbs free energy, ∆G°, of specific adsorption was calculated from the well-known equation:
The values of ∆H˚ and ∆G° are presented in Table 4. Table 4 reveals that the value of ∆H˚ is positive and the value of ∆G° is negative which show that the sorption of cesium on synthesized composite is an endothermic and a spontaneous ion-exchanging process.
Adsorption isotherms
The adsorption isotherm is the equilibrium relationship between the concentration in the fluid phase and the concentration in the adsorbent particles at a given temperature and pH. The adsorption isotherm parameters show actually the surface properties and affinity of the sorbent. Some typical isotherm shapes are shown in the literature as arithmetic graphs. In this paper Langmuir and Freundlich models are applied to calculate the sorption data of Cs+ on STS-PAN.
The Langmuir sorption isotherm has been widely used to characterize the adsorption phenomena from solution. The isotherm is valid for monolayer adsorption onto a surface containing a finite number of identical sites. The form of Langmuir isotherm can be represented by the following equation [25]:
where q e is the amount of metal ion sorbed per unit weight of adsorbent (mol/g), C e the equilibrium concentration of the metal ion in the equilibrium solution (mol/L), Q ∘ the monolayer adsorption capacity and b is the constant that relates to the heat of adsorption.
Freundlich isotherm model stipulate that the ratio of solute adsorbed to the solute concentration is a function of the solution. This model allows for several kinds of sorption sites on the solid and represents properly the sorption data at low and intermediate concentrations on heterogeneous surfaces. The model has the following form [26]:
where K F represents the sorption capacity when metal ion equilibrium concentration equals to 1, and 1/n represents the degree of dependence of sorption with equilibrium concentration.
Figure 9 represents the experimental adsorption isotherm of the intended composite and Figs. 10 and 11 demonstrate the fitted resulting diagrams based on Langmuir and Freundlich equations at 25 °C (298 K). The parameters calculated from the slopes and the intercepts, by means of a linear least square fitting method, are summarized in Table 5. Higher correlation coefficient indicates that the cesium adsorption on the synthesized STS-PAN composite is monolayer and the Langmuir model fits the adsorption data better than the Freundlich model over the entire range of adsorptive concentration studied.
Columnar experiments
Breakthrough diagram
In column fixed bed adsorption, the concentrations in the fluid phase and the solid phase change with time as well as with position in the bed. At first time, most of the mass transfer takes place near the inlet of the bed, where the fluid contact fresh adsorbent. If the solid contains no adsorbate at the start, the concentration in fluid drops exponentially with distance essentially to zero before the end of the bed is reached. After a few minutes, the solid near the inlet is nearly saturated, and most of mass transfer takes place further from the inlet.
In this stage also 0.2 g of STS-PAN composite was put in glass tubes with 0.8 cm diameter and 60 cm long. Then 200 mL of effluent containing Cs+ together with tracer, with 50 ppm concentration was passed through the tube. The concentration gradient, A i/A f, becomes S-shaped versus time, where A i is Cs effluent activity (Bq/mL) and A f is Cs feed activity (Bq/mL). Cesium breakthrough curve was generated from columnar test A i/A f, by plotting the number of bed volumes (BV) of feed processed against the percent breakthrough A i/A f × 100%. The region where most of the change in concentration occurs is called the mass transfer zone, and the limits are often taken as A i/A f, equal to 0.95 to 0.05.
Solutions were made using water sample taken from river near capital city of Iran, Tehran. Table 6 represents the analytical results of its water. It is noteworthy that this river is seasonal, so during the other seasons has little water or is even dry.
Figure 12 shows breakthrough curve on STS-PAN composite. To provide an estimate of dynamic capacity, a second order kinetic equation was fit to the data set to obtain a relationship for Cs effluent concentration as function of throughput volume. This equation for Cs concentration was then substituted into following relationship for dynamic capacity (DC):
where υ is volume at specified breakthrough, and M is mass of STS-PAN sorbent (g dry). Dynamic capacity estimated was then obtained by evaluating the integral numerically with upper limit values corresponding to approximately 5 and 100% Cs breakthrough. Adsorption dynamic capacity of the synthesized composite in 5 and 100% breakthrough conditions, as well as efficiency of the adsorbent column are presented in the following Table 7. Though the structure of synthesized adsorbent is tunnel-shaped with a very high adsorption level, it is observed that cesium adsorption rate is not so high on the synthesized adsorbent, which this phenomenon is due to high reluctance of sodium ion contained in the adsorbent structure to interact with cesium ion contained in the solution. Due to high contamination of 137Cs ion, practically higher than 5% saturation is used. Sorbent capacities at a flow rate of 15 BV/hr were determined to 9.80 and 22.06 mg Cs/g STS-PAN 5 and 100% Cs breakthrough, respectively. The efficiency formula of adsorbent column is:
where area 1 is the area above the curve from A f/A i = 0% till A f/A i = 5%, and area 2 is the area above the curve from A f/A i = 5% to A f/A i = 100%, the obtained efficiency is approximately about 44.42%.
Elution diagram
For elution studies, a glass column containing 0.2 g of the prepared composite on a glass wool support was loaded with a solution of 10−4 mol/L containing 137Cs tracer. Desorption with 0.1 mol/L HCl solution was carried out at a flow rate of 0.5 mL/min at 25 °C. Fractions of 10 mL were analyzed for 137Cs activity. Figures 13 shows elution curve of cesium from STS-PAN composite with 0.1 normal HCL solution. As it can be seen about 85% of the adsorbed Cs was eluted with 50 mL eluent. This confirms the difficulties are not encountered in eluting cesium from STS-PAN composite.
Conclusions
The studies showed that the synthesized composite have crystalline structure and was thermally stable, resistant to gamma irradiation of up to 200 KGy. The adsorption properties showed that the adsorption of cesium is directly depended upon the contact time, temperature and pH of the media used, and as these controlling parameters increase, the adsorption of cesium ions for the ion exchanger, increase. The equilibrium data obtained in this study accorded excellently with the Langmuir adsorption isotherm over the entire concentration range investigated. The values of ∆G˚, ∆H˚ and ∆S˚ prove that the sorption of cesium on STS-PAN is an endothermic and a spontaneous process. The overall results indicate the possibility of using the synthesized composite for efficient removal of 137Cs from aqueous solutions. Furthermore, its spherical shape allows it to be used successfully in column separation processes. Complete breakthrough curve was generated at feed rate of 15 BV/hr and sorbent capacities were determined to be approximately 9.80 and 22.06 mg Cs/g STS-PAN, 5 and 100% Cs breakthrough, respectively. In this case the column efficiency was 44.42%. Finally, the elution result confirms that the STS-PAN has good elution characteristic.
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Saberi, R., Nilchi, A., Rasouli Garmarodi, S. et al. Adsorption characteristic of 137Cs from aqueous solution using PAN-based sodium titanosilicate composite. J Radioanal Nucl Chem 284, 461–469 (2010). https://doi.org/10.1007/s10967-010-0499-3
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DOI: https://doi.org/10.1007/s10967-010-0499-3