Abstract
Sorption behavior of strontium ions on manganese oxides obtained by sol–gel technique reduction of KMnO4 by different reagents (H2O2, MnCl2 and polyvinyl alcohol) was studied. Sorption capacity of the most effective sorbent reaches 200 mg g−1 and distribution coefficient Kd (85Sr)—3.67 × 105 cm3 g−1. Ion-exchange and chemisorption mechanism of strontium ions removal by manganese oxides were confirmed by means XRD, FT-IR, N2 adsorption–desorption and SEM–EDX methods. The obtained sorbents are promising for liquid radioactive water treatment from strontium radionuclides.
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Introduction
Radioactive waste contamination of the environment is one of the global ecological problems of our time. This is due to the operation of the nuclear power plants (NPP) and nuclear energy facilities, which leads to the formation of large amounts of liquid radioactive waste (LRW) that require processing and decontamination [1,2,3]. For example, operation of NPP based on the fast neutron reactor with electrical capacity of 600 MW results to annual discharges of radionuclides with waste water in volume 81 000 m3, with a total activity about 3.9 × 1011 Bq [4]. One of the long-living radionuclides included in the LRW and which pose a significant threat to human and living organisms is the radionuclide 90Sr [5, 6]. The half-life of 90Sr isotope is 28.79 years. Chemical properties of Sr2+ are similar to Ca2+ ions, which complicates the task of purification of LRW and requires the development of materials for selective removal of Sr2+ ions from multicomponent aqueous solutions with high salinity.
Adsorption is the most effective and economically feasible method of purification of aqueous solutions containing trace amounts of Sr2+ [7,8,9,10]. In addition, this method allows selectively extract Sr2+ ions and its radionuclides from real polluted aquatic medium and LRW, thereby most effectively minimizing the amount of waste generated. In recent years, polymeric adsorbents functionalized with organic various acids have been used to control adsorption capacity and to provide selective adsorption of Sr2+ ions from aqueous solutions [11,12,13]. At the same time, inorganic sorption materials (zeolites, clays, metal oxides, etc.) have certain advantages over organic ion exchangers when using for treatment of liquid radioactive wastes due to their high chemical (pH range 0–14 and 2–12, respectively) and radiation stability (more than 108 Gray (Gy) and 105–106 Gy, respectively), compatibility with likely immobilization matrices such as cement and selectivity in relation to Sr2+ ions [14,15,16,17]. It is important to note that the selective properties are determined by the nature of the matrix of the sorbent, state of radionuclides in the aquatic environment, nature and concentration of related compounds [18].
High exchange capacity, stability in alkaline media allow to consider manganese oxides with a layered and channel structure as a promising materials for the removal of radioactive metal ions from aqueous media [19]. Moreover, the performance of manganese oxides in comparison with inorganic sorbents (such as zirconium phosphate, titanium phosphate and titanium dioxide, which decreased at dose 2.19 MGy) and organic sorbents (efficiency is significantly reduced by doses of 0.1–1.0 MGy) is maintained up to the irradiation with dose 10 MGy [20]. Manganese oxides have a structure of octahedral molecular sieves (OMS) with tunnels 2 × 2 or 3 × 3, which is formed from octahedra MnO6 [21, 22]. The dimensions of the tunnels of OMS-2 (cryptomelane with ions K+) and OMS-1 (type todorokite with ions Ca2+ or Mg2+) depend on the cations located inside and around of 0.46 and 0.70 nm respectively [23, 24].
According to the reference study of [25], in comparison with other types of organic and inorganic sorbents, manganese oxides are relatively highly selective towards Sr2+ ions in the presence of Na+, Ca2+ and Mg2+ ions. At sorption from solutions, also containing 0.1 M NaNO3 and 0.01 M Ca(NO3)2, Kd values for sorbent MDM [mixed manganese oxides (III, IV)] are 3.5–4.0 × 104 and 1.5–2.1 × 103 cm3 g−1, respectively. The authors [26] studied the sorption of the radionuclide 85Sr and 137Cs from aqueous solutions (in deionized H2O) on synthetic manganese oxides with tunnel structure. For the oxides of cryptomelane type K Csd and K Srd are equal to 7.4 × 103 and > 106 cm3 g−1, and for oxides of the todorokite type values K Csd and K Srd are 5.0 × 104 and > 106 cm3 g−1 respectively. In reference study of [27] the values of Kd for the materials of composition K2xMnxSn3−xS6 (x = 0.5–0.95), or KMS-1 were determined. The value of Kd in distilled water is equal to 1.58 × 105 cm3 g−1. On the background of complex salt composition containing 3.70 Mg2+, 11.14 Ca2+, 9.17 Cs+, 25.96 Na+ and 4.60 mg dm3 Sr2+ affinity of strontium is greater than for other cations mixture (Kd = 1.83 × 104 cm3 g−1).
This work is devoted to study the mechanism of Sr2+ ions sorption from aqueous solutions onto tunnel manganese oxides obtained by the sol–gel method with the reducing KMnO4 by different reagents—MnCl2, H2O2, PVA. The relationship between the conditions of preparation, physical–chemical and sorption-selective properties of manganese oxides will allow to define general regularities and approaches to the directed synthesis of highly selective sorbents of strontium radionuclides.
Experimental
Manganese oxides synthesis
Sorbents based on manganese oxides were obtained with sol–gel method by reducing KMnO4 in aqueous medium by PVA and inorganic reagents—H2O2 or MnCl2 [28, 29]. To prepare the respective aqueous solutions used distilled water and reagents—KMnO4, H2O2 (30 wt% aqueous solution), MnCl2·4H2O and PVA (fully saponified, state standard 10779-78). All chemicals were of analytical grade and utilized as purchased from Five Oceans (Belarus) without further purification.
To 50 cm3 of 0.1 wt% aqueous solution of KMnO4, various amounts of 1.0 wt% aqueous solution H2O2 (2.2 cm3) and 0.1 wt% aqueous solution MnCl2 (0.4 cm3) solutions were added dropwise with continuous stirring. Molar ratio of KMnO4:H2O2 and KMnO4:MnCl2 equal to 1.00:1.25 and 1.0:1.5, respectively. As a result of getting a dark brown sol with a content of 0.05 wt% MnO2, pH 10.8 and ζ-potential − 21.9 mV (H2O2—reducing agent). In the case of using MnCl2 the content of MnO2 in sol is 0.02 wt%, pH 4.4, ζ-potential − 17.5 mV. Hydrogels were obtained as a result of aging or electrolyte coagulation of sols which were subjected to heat treatment in a laboratory furnace SNOL 7,2/1300 in air at 400 °C for 3 h, the heating rate was 5 °C/min.
Using 0.5 wt% PVA like reducing agent, to 25 cm3 of it, 25 cm3 of KMnO4 solution (0.5 wt%) was added in order to obtain 1.0:1.5 KMnO4/MnCl2 molar ratio.
In the third case, manganese oxide sol was prepared by adding dropwise 0.5 wt% aqueous solution of KMnO4 under vigorous stirring to the 0.5 wt% aqueous PVA solution, the mass ratio of KMnO4:PVA is 1:1. Thus formed colloidal solution is dark brown. The content of MnO2 in sol is 0.33 wt%, pH 10.2, ζ-potential − 25.1 mV. The resulting hydrogel was washed with distilled water, dried in air at room temperature and calcined at 450 °C for 3 h, the heating rate was 5 °C min−1.
Sorption study
Sorption properties of the synthesized sorbents towards Sr2+ ions were studied in static conditions at V/m ratio = 250 cm3 g−1 (V—volume of the solution that contains the sorbed Sr2+ ions (10 cm3); m—mass of the synthesized sorbents (0.04 g) with use of stable strontium ions and 85Sr radionuclide at standard conditions (25 °C, 1 bar). In the first case, sorption of Sr2+ ions was carried out from Sr(NO3)2 solutions [analytical grade, Five Oceans (Belarus)] with concentration of Sr2+ 2000 mg dm−3 and pH 5.6. Concentration of Sr2+ in initial solution and after contact with sorbents (24 h) was defined on atomic absorbing spectrometer AAS Contr AA 300 (Germany). For solution containing radionuclide 85Sr pH value was 5.59. The activity of initial solutions (A0, kBq cm3) and after sorption (Ae, kBq cm3) was carried out on a gamma beta spectrometer of MKS AT1315 (Belarus). For studying of influence of sodium and calcium ions on strontium removal efficiency the aqueous solutions were prepared with addition of 0.1 M NaCl and 0.05 M CaCl2.
Sorption capacity (Q, mg g−1) and distribution coefficient (Kd, cm3 g−1) of 85Sr radionuclide were calculated by the following equations:
where C0 and Ce—initial and equilibrium concentration of Sr2+ ions, mg g−1, respectively, A0 and Ae—initial and equilibrium solutions activity of 85Sr, kBq cm3, respectively, V—volume of solution, dm3, and m—mass of a sorbent, g.
Characterization methods
Measurement of ζ-potential of the dispersed phase of manganese oxide hydrosols was performed at a laser analyzer Zetasizer Nano ZS (Malvern Instruments) at a temperature of 25 ± 0.1 °C.
XRD analysis was carried out by the diffractometer DRON-3 with Cu-Kα-monochromatizing radiation (λ = 0.154184 nm) at reflection angles 2θ from 10 to 80° to identify the phase composition of the sorbents based on manganese oxides used. The processing of diffraction data and phase identification of the samples was carried out using software “PowderX” and “WinXpow” (Version 1.04) and base of X-ray powder standards “JCPDS PDF2” (Version 1.21).
IR spectra of samples were recorded on IR spectrometer with Fourier transmittance Tenzor-27 in the range of 1800–450 cm−1 at room temperature, using a tableting of sorbents powder with potassium bromide.
The adsorption and textural properties of samples were estimated from isotherms of low temperature (− 196 °C) nitrogen physical adsorption–desorption via volumetric on ASAP 2020 MP surface area and porosity analyzer (Micromeritics, United States). The specific surface area was determined by the BET method (ABET). The adsorption cumulative volume (VBJH ads) in the range of pore from 1.7 to 300 nm, the average adsorption diameter (DBJH ads), differential mesopore size distribution (dV/dlogD) calculated by Barrett-Joyner-Halendy method (BJH). Before the analysis samples were held in a vacuum for 1 h at 200 °C and a residual pressure of 133.3 × 10−3 Pa. The samples 1 and 5 were held in a vacuum for 3 h at 80 °C. The relative error in determining the pore volume was ± 1%, for the surface area and for the pore size ± 15%.
The surface morphology and element composition of manganese oxides were studied by means of the scanning electronic microscope of JSM-5610 LV with system of the chemical analysis EDX JED-2201 JEOL (Japan) with a preliminary coating of gold on the samples.
The pH of the reaction mixture and manganese oxides hydrosols was measured using the pH meter HI 221 (HANNA Instruments).
Results and discussion
Sorption properties towards strontium ions
Sorption properties of manganese oxides towards Sr2+ ions at the interface solid/solution substantially depend on the nature of the reducing agent and the conditions of the sorption process. So the sample prepared using H2O2 shows the highest sorption capacity equal to 200 mg g−1 in the absence of background electrolyte (Table 1). The other two manganese oxides samples obtained by reducing of KMnO4 by MnCl2 or PVA have lower capacitive characteristics equal to 70 and 100 mg g−1 respectively.
A similar dependence is observed in the introduction of 0.1 M NaCl to the model solution, when all the samples have almost a threefold decrease in sorption capacity for Sr2+. When take place the sorption from solutions, including the addition of 0.05 M CaCl2, a number of active sorbents based on manganese oxides significantly changes. The high sorption capacity of the sample is obtained using PVA as a reducing agent. On the background of 0.1 M NaCl and 0.05 M CaCl2 this sample demonstrates almost equal to the sorption capacity, about 25–33 mg g−1, while the sorbents obtained using H2O2 or MnCl2 remove in 3–4 times lower Sr2+ amount from Ca2+ containing solutions than Na+ containing (Table 1). This proves a higher selectivity of the manganese oxide synthesized by reducing of KMnO4 by PVA compared with the other samples.
In real conditions low-active liquid radioactive waste contain trace concentrations of radionuclides 85,90Sr (about 10−9–10−13 M). It is obvious that the efficiency of sorption removal of such quantities of Sr2+ may differ significantly from the results obtained during the sorption of stable Sr2+ ions from the solutions with concentration in the range of 10−1–10−4 M. Analysis of the data Table 1 shows that the distribution coefficient of 85Sr for the obtained samples reaches a value of 3.7 × 105 cm3 g−1 with sorption of 85Sr from the solutions without background electrolyte. Such high sorption characteristics of sorbents are quite expected due to absence of the competing ions. The introduction of 0.1 M NaCl is accompanied by a tenfold decrease in the Kd values for 85Sr. The best selective properties (Kd 85Sr = 870 cm3 g−1) on the background of 0.05 M CaCl2 shows a sample obtained using MnCl2. The established differences of the sorption-selective properties of manganese oxides in experiments with stable ions of Sr2+ and radionuclide 85Sr can be interpreted when studying the mechanism of sorption.
XRD analysis
Phase and chemical composition are the main factors that influence on the selective properties of manganese oxides towards Sr2+ ions. The initial sorbents obtained using inorganic reducing agents have low crystallinity and consist mainly K1.33Mn8O16 (96–151–8323—number of phase in COD (“Crystallography Open Database”) and β-MnO2 (96–151–4102) oxides with a layered structure (check Fig. 1a, c). After sorption of Sr2+ in the samples is ongoing structuring and the Sr-containing phase Sr0.72Mn8O16 (41–314) is appeared on the X-ray diffractogrammes (Fig. 1b, d). The sorbent obtained by using PVA consists a well-crystallized oxides K1.33Mn8O16 (96–151–8323) and MnO (96–900–6665) with a mixture of K2CO3 (96–210–7220) (soluble in water—110.5 g in 100 g H2O at 25 °C) and KOH (96–153–4406) (Fig. 1e). The formation of the hydroxide occurs in the interaction of KMnO4 with PVA is mainly at the stage of sol obtaining, which completely fails to wash from the hydrogel of the manganese oxide. Further, the high temperature processing of manganese oxide, during thermo-oxidative degradation of PVA oxidation products, is formed K2CO3. For a sorbent obtained using PVA were detected other Sr-containing phase—SrMnO3 (96–152–9599), SrCO3 (96–901–3803) (soluble in water—2 × 10−3 g in 100 g H2O at 25 °C) and SrO (96–110–1041) in contrast with sorbents synthesized with inorganic reducing agents (Fig. 1f).
Thus, if in the case of manganese oxides obtained using inorganic reducing agents we can talk about a predominantly ion-exchange sorption of strontium ions, the sorption mechanism for the sample on the basis of PVA involves mainly chemical interaction with K2CO3 and to a less degree of ion-exchange.
FT-IR analysis
IR spectra of manganese oxides recorded at the 1800–450 cm−1 before and after sorption of Sr2+ ions allow more detailed study of the sorption mechanism and to identify the differences between the samples (Fig. 2). For all samples after sorption, the intensity of absorption band around 1620 cm−1 which is characteristic for stretching vibrations of O–H groups associated with the manganese atoms of the crystal lattice are raised, indicating the course of hydration process. For the sample synthesized using the H2O2, the intensity of the absorption bands at 613 and 473 cm−1 related to the stretching vibrations of Mn–O characteristic of well-crystallized mixtures of phases (β-MnO2 + γ-MnO2) are significantly increases after sorption of Sr2+ ions. In the case of the reducing agent MnCl2 for initial samples and manganese oxides after sorption a clear band of about 655, 610, 530 and 475 cm−1 which are characteristic of valence fluctuations when the Mn–O in the structure of β-MnO2 are observed. Intense bands at 615 and 480 cm−1 inherent to the stretching vibrations of Mn–O phase in SrMnO3 appear in the sample obtained using the PVA after the sorption of Sr2+ ions. At the same time absorption band with low intensity in the area of 1080 cm−1 corresponding to the stretching vibrations of when the Mn3+–O suggests the partial substitution of Mn4+–Mn3+ ions. The absorption band in the region of 770–750 cm−1 is characteristic of manganese oxides with tunnel structure and it is present in the IR-spectra of all samples [30].
N2 adsorption–desorption study
Nitrogen adsorption results indicate essentially distinctions in characteristic signs and features of the measured isotherms, in hysteresis behavior of adsorptive, in the values of pore volume and surface area of manganese oxide porous solids obtained with different reducers (Fig. 3, Table 2). The nitrogen sorption isotherms on manganese oxide obtained with hydrogen peroxide belong, on IUPAC classification, to the Type IV isotherm given by many mesoporous adsorbents. Isotherms of this type have the same overall shape as a normal Type II isotherm, obtained with non-porous or macroporous adsorbents, up to the value of relative pressure p/p0 at which the capillary condensation begins resulting in the hysteresis loop and adsorption growth. The hybrid Type (H1+H2) hysteresis loop given by “peroxide” sample before sorption of Sr2+ ions correlates with texture of adsorbent. The Type H1 loop is associated with narrow pore size distribution of fairly uniform “cylindrical” mesopores (Fig. 3a). The Type H2 loop indicates more complex porous structure in which the effects of percolation and pore blocking are shown. Nitrogen sorption isotherms for two other samples received with MnCl2 and/or PVA don’t exhibit any limiting adsorption at high p/p0 values and can be carried to pseudo-type II isotherm. Such not completely reversible isotherms, according to Kenneth S.W. Sing, are associated with adsorbents containing slit-shape pores and consisting of friable aggregates of platy particles. Their adsorption curve entirely repeats the path of the Type II adsorption isotherm, but desorption branch follows on other way, leading to the hysteresis limited by area of multilayer adsorption.
Sorption of Sr2+ significantly influences the adsorption and capillary-condensation properties of manganese oxides. So this circumstance considerably affects the properties of xerogel obtained with H2O2. The specific characteristics of surface area and pore volume decrease by 3.3 times after sorption of Sr2 + ions. When using MnCl2 the surface area decreases by 2.9 times after sorption of Sr2+, and in case of PVA the surface area is equal only to 11–24 m2 g−1 and remains poorly developed after sorption of Sr2 + ions. Isotherms of pseudo-type II don’t provide reliable assessment neither specific pore volume, nor pore size distribution. But in the samples received with MnCl2 or with PVA it is possible to record after sorption of Sr2+, first, the decrease in pore volume proportionally to falling surface area, therefore the pore size remains almost invariable (Table 2), and, secondly, the full modification of pore size distribution (Fig. 3b, c). It is undoubted that the displaying Sr2+ sorption in case of the samples obtained with H2O2 and in case of the sample obtained with H2O2 differ one from another. So inclusion of Sr2+ ions into the “peroxide” sample facilitates diffusion of nitrogen molecules in mesopores, and the mean mesopore diameter increases (Table 2). At the same time the pore size distribution of cylindrical mesopores remains uniform after sorption of Sr2+ ions, but pore volume falls (Fig. 3a).
Thus, it should be noted that the growth of the mean mesopore diameter of the “peroxide” sample observed after Sr2+ sorption is obliged to fast loss of surface area in combination with homogeneous “volume shrinkage” of manganese oxide xerogel. Most likely, the positive Sr2+ ions sorbed by ion-exchange with the cations compensating a charge of manganese oxide framework are rather evenly dispersed all over the volume of crystals what SEM–EDX analysis data confirm.
SEM–EDX analysis
The results of SEM–EDX analyses prove that in the case of the manganese oxide obtained by reduction of KMnO4 by H2O2, Sr2+ is distributed uniformly across the surface of the sorbent with the presence of small areas with higher content of Sr2+ component. On the sample obtained with MnCl2 Sr2+ is appeared very weak which indicates about it low content. The highest Sr2+ content determined on the surface of the sorbent is detected in the sample obtained using PVA. In the pictures clearly seen as Sr2+ concentrates on separate sites of manganese oxide surface in the form of individual phases. Combined with the XRD data we can assume that it is the particles of SrCO3 (Fig. 4).
According to the element analysis of the manganese oxides before and after sorption of Sr2+ ions, in all samples observed the expected decrease in the K+ content and identification of Sr2+ in the range of 1.0 at.%. It was revealed that the number of Sr2+ ions in the sample, synthesized using PVA significantly greater than that of manganese oxides obtained with inorganic reducing agents. These results are in a good agreement with the ion-exchange or chemisorption mechanism of strontium uptake onto manganese oxides obtained using either inorganic reducing agent (H2O2, MnCl2), or PVA respectively (Table 3).
Conclusions
The manganese oxides sorbents of Sr2+ ions were synthesized by sol–gel method reducing of KMnO4 by different reagents—H2O2, MnCl2 and PVA. Their sorption characteristics towards stable (Sr2+) and radioactive (85Sr) ions were established. The sorbent obtained using H2O2 as a reducing agent has highest sorption properties (sorption capacity 200 mg g−1 and Kd 85Sr 3.67 × 105 cm3 g−1). Manganese oxide obtained using H2O2 provides the most selective removal of Sr2+ ions in presence of 0.1 M NaCl (sorption capacity 78 mg g−1 and Kd 85Sr 4.74 × 104 cm3 g−1). In presence of 0.05 M CaCl2 sorbent synthesized using PVA has the highest sorption capacity—33 mg g−1 and the sample obtained using MnCl2 has the highest Kd 85Sr—8.70 × 102 cm3 g−1.
On the basis of XRD, FT-IR, N2 adsorption–desorption and SEM–EDX data was proposed a possible mechanism of Sr2+ ion uptake by manganese oxides. In case of manganese oxides obtained with inorganic reducing agents (H2O2 and MnCl2) Sr2+ ions are removed dominantly by ion-exchange mechanism. For samples, obtained using PVA a chemisorption mechanism was proposed. It has been confirmed with the formation of SrMnO3 and SrCO3 while ion-exchange mechanism—with the replacement of K+ and Mn2+ ions in K1.33Mn8O16 on Sr2+. It was shown that obtained sorbents are promising for liquid radioactive water treatment from Sr radionuclides.
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This work was financially supported by the State Program of Scientific Research (grant# 1.05).
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Ivanets, A.I., Prozorovich, V.G., Kouznetsova, T.F. et al. Sorption behavior of 85Sr onto manganese oxides with tunnel structure. J Radioanal Nucl Chem 316, 673–683 (2018). https://doi.org/10.1007/s10967-018-5771-y
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DOI: https://doi.org/10.1007/s10967-018-5771-y