Sorption of Eu(III) on Fe–montmorillonite relevant to geological disposal of HLW

2018 ◽  
Vol 106 (12) ◽  
pp. 971-983 ◽  
Author(s):  
Santosh Chikkamath ◽  
Madhuri A. Patel ◽  
Aishwarya S. Kar ◽  
Vaibhavi Raut ◽  
Bhupendra Singh Tomar ◽  
...  

Abstract Montmorillonite (Mt) is the major clay mineral of bentonite, which is the candidate buffer material in the engineered barrier system for geological disposal of high level waste (HLW). The alteration of Mt due to its interaction with carbon steel (overpack) can produce Fe–Mt. In order to understand the basic properties of Fe–Mt, the sorption studies using Eu(III) are reported here. For this, Fe(III)–Mt was prepared by conventional cation exchange method using FeCl3 with Na–Mt. The obtained Fe(III)–Mt was then reduced to Fe(II)–Mt using ascorbic acid. Both the samples were characterized based on their X-ray diffraction, Fourier transform infrared spectra, cation exchange capacity and specific surface area. The batch sorption studies of Eu(III) were conducted for both Fe(III)–Mt and Fe(II)–Mt as a function of pH (3–10), ionic strength (0.001 M–1 M) and Eu(III) concentration (10−8–10−3 M). The distribution coefficient (Kd) was found to be higher for Fe(III)–Mt compared to Fe(II)–Mt and Na–Mt. The sudden increase in sorption in the pH range 4.5–6 and remaining constant beyond it indicates ion exchange mechanism at pH<4.5, with surface complexation mechanism dominating the sorption at pH>4.5. This is further corroborated by ionic strength dependent sorption data which shows decrease in sorption capacity of Fe–Mt with increasing ionic strength at low pH, but remaining more or less unchanged at higher pH. Eu(III) adsorption isotherm on Fe–Mt increased linearly with [Eu(III)] reaching saturation at 10−5 M and 10−4 M for Fe(III)–Mt and Fe(II)–Mt, respectively. The amount of iron released from Fe–Mt and Fe(II)/Fetotal during sorption were estimated to understand the effect on Eu(III) sorption behaviour by release of interlayer iron in Fe–Mt.

Soil Research ◽  
1979 ◽  
Vol 17 (1) ◽  
pp. 129 ◽  
Author(s):  
GP Gillman

The 'compulsive exchange' method of Bascomb has been modified to allow the determination of cation exchange capacity and anion exchange capacity of soils containing significant quantities of constant potential surfaces. The soil is equilibrated with unbuffered barium chloride solution at an ionic strength approximating that of the soil solution, so that the conditions under which determinations are made are similar to those found in the field. Barium on the exchange complex is then replaced by magnesium when the latter is added as magnesium sulfate, and this is accomplished without altering the solution ionic strength. If desired, exchangeable basic cations can be determined as an additional step in the procedure. Results obtained by the proposed method are compared with other commonly used procedures for determining cation exchange capacity and exchangeable basic cations.


Materials ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1173
Author(s):  
Fotini Martsouka ◽  
Konstantinos Papagiannopoulos ◽  
Sophia Hatziantoniou ◽  
Martin Barlog ◽  
Giorgos Lagiopoulos ◽  
...  

Six pharmaceutical pastes were prepared using chemically modified kaolin and talc powders. Tests were conducted to determine their structural and chemical characteristics as well as their antimicrobial protection, thus rendering them suitable for cosmetic and pharmaceutical uses. Kaolin and talc were treated chemically via the cation exchange method to load the clay particles with copper and zinc ions, two cations well known for their antimicrobial properties. Mineralogical analyses were conducted by using X-ray diffraction (XRD) before and after the modification, confirming the mineralogical purity of the samples. Scanning electron microscopy was also used in conjunction with energy dispersed spectroscopy (SEM-EDS) to obtain chemical mapping images, revealing the dispersion of the added metals upon the clay minerals surfaces. Moreover, chemical analysis has been performed (XRF) to validate the enrichment of the clays with each metal utilizing the cation exchange capacity. All modified samples showed the expected elevated concentration in copper or zinc in comparison to their unmodified versions. From the X-ray photoelectron spectroscopy (XPS), the chemical state of the samples’ surfaces was investigated, revealing the presence of salt compounds and indicating the oxidation state of adsorbed metals. Finally, the resistance of pastes in microbial growth when challenged with bacteria, molds, and yeasts was assessed. The evaluation is based on the European Pharmacopeia (EP) criteria.


Soil Research ◽  
1981 ◽  
Vol 19 (1) ◽  
pp. 93 ◽  
Author(s):  
GP Gillman

The cation exchange capacity of six surface soils from north Queensland and Hawaii has been measured over a range of pH values (4-6) and ionic strength values (0.003-0.05). The results show that for variable charge soils, modest changes in electrolyte ionic strength are as important in their effect on caton exchange capacity as are changes in pH values.


1987 ◽  
Vol 76 (2) ◽  
pp. 221-228 ◽  
Author(s):  
Masanori Takahashi ◽  
Masayuki Muroi ◽  
Atsuyuki Inoue ◽  
Masahiro Aoki ◽  
Makoto Takizawa ◽  
...  

Clay Minerals ◽  
2013 ◽  
Vol 48 (2) ◽  
pp. 215-233 ◽  
Author(s):  
R. Dohrmann ◽  
S. Olsson ◽  
S. Kaufhold ◽  
P. Sellin

AbstractBentonites are candidate materials for the encapsulation of radioactive waste. In the ‘Alternative Buffer Material test’ (ABM), compacted ring-shaped blocks of eleven different buffer materials (mainly bentonites) were packed vertically on top of each other with an iron tube as heater in the centre. These buffer materials started with various exchangeable cation populations (ECpopulation). The first ‘ABM package’ was terminated 28 months after installation and the bentonites had been exposed to the maximum temperature (130°C) for about one year. The aim of the present study is first: to describe modification of the cation exchange population, and second to understand the influence of the groundwater on cation exchange at different scales. No significant horizontal variation of any exchangeable cation (EC) was detected between 1 and 7 cm distance from contact with the iron tube. Large total differences of the ECpopulations, however, were observed for the individual blocks after the field experiment (n = 21 blocks) with respect to the composition of the reference materials. The average cation exchange capacity (CEC) values of the analysed bentonites (n = 9 blocks) decreased by 5.5 meq/100 (1.1 – 8.8 meq/100 g) after the experiment. Exchangeable Na+ and Mg2+ decreased on average, whereas Ca2+ increased. This trend was pronounced in the top region of the parcel (upper seven blocks). Although most changes occurred on the large scale of the whole test parcel, small but important changes were also recorded in the vertical direction on the centimetre scale. The observed differences cannot be explained assuming simply that a bentonite reacts only with neighbouring blocks, which would mean that the system was more or less closed. The differences are much larger and the only conclusion from this observation is that the whole package seems to be influenced by the groundwater which was added from a water tank at the experiment site, enabling at least partial equilibration between the different blocks.


Author(s):  
F. B. Okanlawon ◽  
O. O. Awotoye ◽  
P. O. Ogunbamowo

Aims: This study aimed at demonstrating the adsorption capacity as well as the removal of glyphosate and cadmium unto Alfisols. Place and Duration of Study: Research was carried out in Analytical Laboratory of Department of Chemistry, University of Ibadan, Nigeria. The soil sample was collected from an undisturbed forest land, University of Ibadan, Nigeria. Methodology: The soil sample was air dried for 72 hours under ambient temperature and allowed to pass through 2 mm sieve before use. All solutions and soil dispersions were prepared using de-ionised water. The pH, organic carbon, particle size, exchangeable cations, cation exchange capacity, available phosphorus and soil total nitrogen were all analysed for in the soil sample following the standard procedures likewise the cadmium and glyphosate adsorption/adsorbent studied. Results: The pH of the soil is slightly acidic with high total organic carbon, while the cation exchange capacity is on the lower side. The textural class of the soil greatly influences its water retention capacity, thus the soil under study is predominantly sandy. A decrease in the equilibrium adsorption capacity was observed when the adsorbent dose was increased from 0.2 – 0.8 g however, with a sharp increase at a dose of 1 g. An increase in the percentage cadmium removal was observed with increase in pH from 48.80% to a maximum of 91.10% at neutral pH. The result also indicates that increasing the initial concentration of the cadmium ions and glyphosate lead to an increase in the uptake capacity of the soil for both adsorbate. At higher ionic strength of 0.1 M, the peak removal was obtained at initial concentration of 10 ppm which eventually attains equilibrium at other concentration level. Conclusion: Alfisol can therefore concluded to be an adsorbent provided some conditions like a low cadmium concentration, a neutral pH and a higher adsorbent dosage are adhere too. While glyphosate removal, a pH of 5 and higher ionic strength of KNO3. is required.


1988 ◽  
Vol 127 ◽  
Author(s):  
Volker Koss

ABSTRACTThe sorption of nickel in 15 natural sediment-groundwater systems from Gor leben has been modeled using a simple surface complexation model. An apparent constant of nickel sorption has been computed taking into account the bulk cation exchange capacity of the sediment, the analytical composition of the groundwater and experimental sorption data obtained from related systems. The method of determining the prevailing surface complex has been described in detail, using changing properties of the natural systems. Competition from natural groundwater components for sorption sites has been taken into account.The main parameters governing nickel sorption are cation exchange capacity of the sediment, together with ionic strength and pH of the groundwater. The model describes the influence of citrate on sorption and allows one to compare the varying sorption data of similar systems.Computations were performed using the geochemical code MINEQL.


Soil Research ◽  
2002 ◽  
Vol 40 (5) ◽  
pp. 781 ◽  
Author(s):  
M. Escudey ◽  
P. Diaz ◽  
J. E. Förster ◽  
G. Galindo ◽  
C. Pizarro ◽  
...  

The Gaines-Thomas formulation of the Rothmund-Kornfeld equation was used to predict the K-Ca-Mg exchange in variable surface charge soils. Binary and ternary equilibria were carried out at 25°C and at constant ionic strength of 0.050 mol/L. The selectivity sequence K &gt; Ca &gt; Mg was observed in binary isotherms. The experimental ternary isotherms are well described from binary data. When experimental v. calculated equivalent fractions were plotted, slopes between 0.901 and 1.051, and correlations between 0.970 and 0.986, were obtained. The design used assures in volcanic soils that no, or minor, changes in surface charge, cation exchange capacity, and selectivity occur, but the predicted ternary values are restricted to the same binary experimental conditions employed.


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