Abstract
Titanate nanotubes (TNTs) have been synthesized by a hydrothermal method using rutile TiO2 powder as titanium source. The determination of the structure and morphology was characterized by XRD, FTIR, SEM and TEM. The results indicate that the TNTs successfully synthesized under hydrothermal conditions of 150 °C. The adsorption of Th(IV) on TNTs was studied as a function of contact time, pH values, ionic strength, initial Th(IV) concentration and temperature under ambient conditions by using batch technique. The results indicate that adsorption of Th(IV) on TNTs is strongly dependent on pH values, but weakly dependent on ionic strength; Adsorption kinetics was better described by the pseudo-second-order model. The adsorption isotherms are simulated by Langmuir and Freundlich models well. ΔG°, ΔH° and ΔS° free energy were calculated from experimental data, The results indicate that the adsorption of Th(IV) on TNTs is an endothermic and a spontaneous process, and increases with increasing temperature. The adsorption of Th(IV) on TNTs is mainly dominated by chemical sorption or surface complexation.
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Introduction
Thorium is a naturally radioactive element widely distributed over the earth’s crust. It has been widely used in nuclear fuel industry, alloy, and laboratory investigations [1]. But thorium is long-lived radionuclides with a suite of radioactive daughter products which can pose a human health and ecosystems risk [2]. Therefore, the removal and recovery of thorium from contaminated water is an urgent and essential work. Various methods including chemical precipitation [3], solvent extraction [4], ion exchange [5] and adsorption [6–13] are effective methods to remove thorium from aqueous solution. Among these methods, adsorption is an efficient and convenient method because of its cost effective treatment, easy operation, no chemical reagents needed and no sludge produced [14]. Numerous adsorbents have been used for the removal of thorium from the aqueous solution, such as natural and modified clays [6], carbon materials [7, 8], biosorbents [9], molecular sieves [10], various resins [11] and other specific materials [12, 13].
Recently, Titanate nanotubes has attracted great interest in nuclear waste management because of their large surface area, more surface atom and the surface rich in hydroxyl groups [15]. TNTs not only have exhibited great potential for the adsorption of heavy metal ions Cu(II) [16], Ag(I) [17], Pb(II) [17, 18], Cd(II) [19], Cr(II) [19], As(III) [20], but also have showed high adsorption capacity in the removal of U(VI) [21], Eu(III) [22], 63Ni(II) [23] from aqueous solution. However, the investigation of radionuclides adsorption on TNTs is still scarce, and the adsorption mechanism is still unclear.
Herein, the adsorption of Th(IV) on TNTs was investigated by using batch technique. The objectives of this work was: (1) synthesized and characterized the TNTs; (2) to study the effect of contact time, pH values, ionic strength and temperature on the Th(IV) adsorption on TNTs; (3) to describe Th(IV) adsorption isotherms with Langmuir and Freundlich models; (4) to calculate the thermodynamic parameters of Th(IV) adsorption, such as ΔG°, ΔH° and ΔS°; (5) to evaluate the adsorption mechanism of Th(IV) on TNTs.
Experimental
Reagents and apparatus
All chemical reagents used in the experiments were purchased as analytical reagent grade and used without any further purification. All solutions in this experiment were prepared using Milli-Q deionized water. The stock solution of Th(IV) (1 mg mL−1) was prepared by dissolving 1.1895 g of Th(NO3)4·4H2O in 30 mL (1+2) HCl, and then the solution was transferred into a 500 mL volumetric flask and diluted to the mark with Milli-Q deionized water to produce a Th(IV) stock solution. A 721-E spectrophotometer (Shanghai, China) was used for the determination of the Th(IV). pHS-3C (Shanghai, China) pH meter was used for pH adjustment. The FTIR spectra were carried out using a Nicolet 380 spectrophotometer in pressed KBr pellets (50 mg KBr and 1 mg of TNTs). X-ray powder diffractometry were carried out using an Shimadzu XRD-6000 diffractometer with Cu Kα radiation. Scanning electron microscopy (SEM) images were obtained with a JEOL JSM-6700F. Transmission electron microscopy (TEM) images were obtained with a JEOL JEM-2010.
Synthesis of TNTs
TNTs were synthesized via a hydrothermal method of 3 g rutile TiO2 nanopowder was mixed with 120 mL 10 mol L−1 NaOH aqueous solution and stirred for 60 min at room temperature. Subsequently heated in a 200 mL Teflon-lined stainless steel autoclave at 150 °C for 48 h, then the reaction vessel was cooled to room temperature and subsequently washed by 0.1 M HCl aqueous solution and Milli-Q deionized water respectively until the pH of rinsing solution was approximately 7.0. The obtained precipitate was dried in a vacuum oven at 90 °C for 12 h and stored in glass bottles until used.
Batch sorption experiments
The adsorption experiments were carried out by batch technique in polyethylene centrifuge tubes under ambient conditions at 298.15 ± 2 K. The stock solution of TNTs and NaClO4 were pre-equilibrated for 4 h before the addition of Th(IV) stock solution. The pH was adjusted to desired values by adding negligible volumes of 0.1 mol L−1 HCl or 0.1 mol L−1 NaOH to achieve the desired pH values. After equilibrium, the pH of the suspension was measured and the samples were centrifuged at 10000 rpm for 30 min to separate the solid and liquid phases. Then the supernatant solution was measured for residual Th(IV) concentration. The concentration of Th(IV) was analyzed by spectrophotometry at 660 nm by using Th(IV) Arsenazo(III) complex [11]. The blank experiments demonstrated that the adsorption of Th(IV) on the polyethylene tube walls was negligible. The amount of adsorbed Th(IV) and distribution coefficient (K d) was estimated from the difference of the Th(IV) concentration in the aqueous before and after the adsorption.
where q (mg g−1) is the amount of Th(IV) adsorbed on TNTs; C 0 (mg mL−1) is the initial concentration of Th(IV) in the solution; C e (mg mL−1) is the concentration of Th(IV) in supernatant after centrifugation; m (g) is the mass of TNTs and V (mL) is the volume of aqueous solution.
Results and discussion
XRD analysis
The X-ray diffraction (XRD) pattern of the sample is shown in Fig. 1. The remarkable diffraction peaks at 2θ = 10.5° is represented interlayer space of TNTs [22, 24], The peaks at 2θ = 28.4°, 24.3° and 48.3° is perhaps the structure of sodium titanate, indicating that the remnant Na+ stabilized the nanotube structures [25].
FTIR analysis
Study of the as-synthesized TNTs was also followed by FTIR in the range between 4000 and 400 cm−1 and the results obtained have been illustrated in Fig. 2. Absorption peak at 400–800 cm−1 can be assigned to the stretching vibration of Ti–O or Ti–O–Ti [26]. A broad and intense band in the region of 3200–3550 cm−1 can be ascribed to O–H stretching vibrations, existence of hydroxyl groups and huge amount of water molecules in the surface and interlayer space. The sharp peak at 1650 cm−1 confirmed the presence of water and can be assigned to H–O–H bending vibrations of water molecules.
SEM and TEM analysis
The morphology of the sample is characterized by SEM and TEM. Figure 3a shows the SEM image of the as-synthesized TNTs, it is indicated that the as-synthesized TNTs are interlaced each other. The nanotube length ranges from several tens to hundreds of nanometers. Figure 3b shows the TEM image of the as-synthesized TNTs, revealing large quantity of tubular materials with narrow size distribution. The tubes are central hollow and open ended. The inner diameter of the TNTs is found to be about 5–7 nm and outer diameter of 9–13 nm.
Kinetics of adsorption
The adsorption of Th(IV) on TNTs has been investigated as a function of contact time. As shown in Fig. 4, The amount of adsorbed Th(IV) soars with time increase, and equilibrium is maintained between two phases after about 8 h. The quick adsorption of Th(IV) suggests that chemical adsorption rather than physical adsorption contributes to Th(IV) adsorption on TNTs [10]. 12 h are enough to achieve the adsorption equilibrium in our experiments. In the subsequent experiments, the contact time of 12 h was fixed for adsorption equilibration of Th(IV) on TNTs. In order to investigate the mechanism of adsorption the kinetics of adsorption has to be studied, the pseudo-second-order rate equation was used to simulate the kinetic adsorption [27]:
where k (g mg−1 min−1) is the rate constant of the model, q t (mg g−1) is the amount of Th(IV) on TNTs at contact time t (min), q e (mg g−1) is the equilibrium adsorption capacity. Linear plot feature of (t q −1t ) versus t is shown in Fig. 5. The data was fitted by the pseudo-second-order rate equation with \( y = 0.0054X + 0.039 \). The q e and k values calculated from the slope and intercept were 185.18 mg g−1 and 7.47 × 10−4 g mg−1 min−1, respectively. The regression coefficients (R 2 = 0.99) for the linear plot is very close to 1, which indicates that the experimental data can be described by the pseudo-second-order rate model well.
Effect of initial pH and ionic strength
Figure 6 shows the distribution of Th(IV) as a function of pH values in aqueous solution. We can see that, at pH ≤ 2.5, Th4+ is more than 70 %, Th(OH)3+ is less than 30 %; at pH ≤ 3.0, Th4+ is less than 35 %, Th(OH)3+ is less than 45 %, Th(OH) +3 and Th(OH)4 is less than 0.3 %; at pH ≤ 4.0, Th4+ is less than 2 %, Th(OH)3+ is less than 17 %, Th(OH) 2+2 is less than 54 %, Th(OH)4 and Th(OH) +3 is less than 14 %. At high pH values, Th(OH)4(aq) could form Th(OH)4 precipitation (K sp = 2 × 10−45), which loses one or two water molecule to form ThO(OH)2 (K sp = 5 × 10−24) and ThO2 precipitation. Östhols [28] found that Th(OH)3CO3 − and Th(CO3) 6−5 can be negligible at pH range 2–4.5, while the hydrolysis products and the precipitation at pH > 4 must play an important role in the adsorption of Th(IV). Thereby, Th(OH)3CO3 − and Th(CO3) 6−5 can be negligible at pH ≤ 3 in this experiments.
The adsorption of Th(IV) on TNTs in 0.01 mol L−1 NaClO4 solution as a function of pH is shown in Fig. 7. Adsorption of Th(IV) is strongly dependent on pH values. Adsorption of Th(IV) increases at pH 1–4, and then maintains its maximum level with increasing pH values. The typical pH dependence adsorption was also found for the adsorption of Th(IV) on TiO2 nanoparticles [13]. The variation of pH before and after adsorption was also measured. The pH values of the solution after adsorption changes a little to the acidic region, which indicates that H+ is released during the adsorption. The adsorption of Th(IV) depends on the number of hydroxyl groups on TNTs surfaces and the concentration of hydroxyl groups is controlled by pH. At pH < 7, ≡ TiOH is the primary hydroxyl groups in TNTs [13, 22], and the Th4+,Th(OH)3+ and Th(OH) 2+2 is the predominating species in Th(IV) solution. The exchange reaction of metal cations with the hydroxyls on the surfaces is presumed as:
The positively charged Th4+, Th(OH)3+ and Th(OH) 2+2 species in solution may exchange with −H from ≡TiOH groups of the hydrolyzed TNTs. The H+ is released from TNTs to solution and thus the pH decreases after equilibration. Similar results were also reported for the adsorption of Eu(III) on TNTs [22].
The adsorption of Th(IV) on TNTs at pH 3.0 as a function of NaClO4 concentrations is shown in Fig. 8. As can be seen that the adsorption of Th(IV) decreases a little with increasing NaClO4 concentration. This suggests that Th(IV) adsorption is weakly dependent on ionic strength. The weakly dependence adsorption of Th(IV) onto TNTs on ionic strength and strongly dependence adsorption on pH values indicate that the adsorption mechanism of Th(IV) is chemical adsorption or surface complexation but ion exchange [6, 29]. In general, surface complexation is influenced by pH values, whereas ion exchange is mainly influenced by ionic strength [30, 31].
Adsorption isotherms
The adsorption isotherm is the equilibrium relationship between the concentration in the fluid phase and the concentration in the sorbent particles at a given temperature and pH. The adsorption isotherm parameters show actually the surface properties and affinity of the sorbent. Langmuir and Freundlich equations are the most frequently used for describing adsorption isotherms.
The Langmuir model assumes that there is no interaction between the adsorbate molecules and the adsorption is localized in a monolayer. The Freundlich equation is an empirical equation employed to describe the heterogeneous systems and is not restricted to the formation of the monolayer. The form of Langmuir isotherm and Freundlich isotherm can be represented by the following equation [32, 33]:
where q m (mg g−1) is the maximum adsorption capacity and b (L mg−1) is the Langmuir adsorption constant that relates to the energy of adsorption; K F (mg1−n g−1 Ln) is the Freundlich constants which are indicators of adsorption capacity, and 1/n represents the degree of adsorption dependence at equilibrium concentration [34].
Figures 9 and 10 demonstrate the fitted resulting diagrams based on Langmuir and Freundlich equations. The slopes and intercepts of the linear Langmuir and Freundlich plots are used to calculate the Langmuir and Freundlich parameters were tabulated in Table 1. The value of R 2 showed that the adsorption isotherms are simulated by Langmuir and Freundlich models well. The value of 1/n indicates a favorable adsorption at 0 < 1/n < 1. The 1/n value of the adsorption of Th(IV) on TNTs is 0.31, which indicates that the adsorption process can be easily taken place [29, 35, 36].
Process thermodynamic parameters
Temperature is an important parameter that dominates the physicochemical behavior of metal ions in the environment. Variation of standard thermodynamic parameters during the adsorption process was evaluated using the following equations [37]:
where ΔS°, ΔH° and T are the standard entropy, standard enthalpy, and temperature in Kelvin, respectively, and R (8.314 J mol−1 K−1) is the gas constant. Thermodynamic parameters (ΔG°, ΔH° and ΔS°) associated with the adsorption of Th(IV) on TNTs were calculated by using this plot of ln K d versus 1/T and Eqs. (8) and (9). The values of thermodynamic parameters for the adsorption of Th(VI) at different temperature were given in Table 2. Table 2 reveals that the value of ΔH° is positive which shows that the adsorption of Th(IV) on TNTs is an endothermic process,and high temperature is advantageous for Th(IV) adsorption onto TNTs. One possible explanation to this positive enthalpy is that the adsorption of Th(IV) can be done in two process: first, the hydration shell surrounding of Th(IV) dehydration to form a single Th(IV) ion, this process needs energy; Then the adsorption of Th(IV) on TNTs by surface complexation, energy will be released in this process; The energy required for the former process exceeds the energy released in the later process, and therefore adsorptions become endothermic [8, 38].
The negative value of ΔG° shows that the adsorption of Th(IV) on TNTs is a spontaneous process. The value of ΔG° becomes more negative at higher temperature, which indicates that more efficient adsorption at higher temperature.
Conclusion
Analysis of the results revealed that the TNTs successfully synthesized under hydrothermal conditions of 150 °C. The adsorption of Th(IV) on TNTs is fast and rate of adsorption can be fitted well by pseudo-second-order kinetic model. The Langmuir isotherm model fits the adsorption data better than the Freundlich model. The adsorption of Th(IV) on TNTs is strongly dependent on pH values, but weakly dependent on ionic strength; The adsorption of Th(IV) on TNTs is an endothermic and a spontaneous process which becomes more favorable at higher temperature. Experimental results provide the evidence that the adsorption of Th(IV) on TNTs may be mainly attributed to chemical adsorption or surface complexation. The results of the experimental studies showed that TNTs have a high potential for application in the removal of Th(IV) from aqueous solution.
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Financial supports from National Natural Science Foundation of China (21203022; 21261001) is acknowledged.
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Liu, J., Luo, M., Yuan, Z. et al. Synthesis, characterization, and application of titanate nanotubes for Th(IV) adsorption. J Radioanal Nucl Chem 298, 1427–1434 (2013). https://doi.org/10.1007/s10967-013-2607-7
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DOI: https://doi.org/10.1007/s10967-013-2607-7