scholarly journals Sorption Characteristics of 137Cs and 90Sr into Rembang and Sumedang Soils

2018 ◽  
Vol 16 (3) ◽  
pp. 277 ◽  
Author(s):  
Budi Setiawan ◽  
Yusran Dani ◽  
Nurmaya Arofah
Keyword(s):  
Ionic Strength ◽  
Soil Sample ◽  
Metal Ion ◽  
Solid Phase ◽  
Radioactive Waste Disposal ◽  
Sorption Behavior ◽  
Planning And Design ◽  
Kd Values ◽  
Important Input ◽  
Radionuclide Activity

In order to understand the sorption behavior of 137Cs and 90Sr into soil sample from Rembang and Subang, it is important to estimate the effect of contact time, ionic strength and concentration of metal ion in the solution. For this reason, the interaction of 137Cs and 90Sr with soil sample has been examined. The study performed at trace concentration (~10-8 M) of CsCl and SrCl2, and batch method was used. NaCl has been selected as a representative of the ionic strength with 0.1; 0.5 and 1.0 M concentrations. Concentration of 10-8~10-4 M CsCl and SrCl2 were used for study the effect of Cs and Sr concentrations in solution. Apparent distribution coefficient was used to predict the sorption behavior. The sorption equilibrium of 137Cs and 90Sr into soil was attained after 5 days contacted with Kd value around 3300-4200 mL/g, where Kd was defined as the ratio of number of radionuclide activity absorbed in solid phase per-unit mass to the number of radionuclide activity remains is solution per-unit volume. Presence of NaCl as background salt in the solution affected Kd values due to competition among metal ions into soil samples. Increase of Cs or Sr concentration in solution made Kd value decreased drastically. This information is expected could provide an important input for the planning and design of radioactive waste disposal system in Java Island in the future.

scholarly journals Sorption of Pb2+, Cu2+ and Zn2+ from Aqueous Solution Using a Blended Membrane of Immobilized Karkashi (Sesame Leaves) and Sodium Alginate

2020 ◽  
pp. 21-29
Author(s):  
Ibrahim Maradona ◽  
J. H. Kanus ◽  
M. Suleman Stephen
Keyword(s):  
Aqueous Solution ◽  
Ionic Strength ◽  
Metal Ions ◽  
Sodium Alginate ◽  
Metal Ion ◽  
Vital Role ◽  
Ion Uptake ◽  
Ion Concentration ◽  
Sorption Behavior ◽  
Blended Membrane

Sorption techniques are widely used to remove heavy metal ions from large volume of aqueous solutions, this plays a vital role in controlling environmental pollution. Herein, the sorption of Pb2+, Cu2+ and Zn2+ with blended membrane of sodium alginate (Na-Alg) and immobilized karkashi leaves (IKAL) from aqueous solution was investigated at optimum conditions for effectiveness. Sorption capacities of the membrane for Pb2+, Cu2+ and Zn2+ were found to be 86.80, 40.60 and 39.55% respectively. The sorption behavior with respect to initial pH, ionic strength, temperature, contact time and initial metal ion concentration was investigated for optimum sorption conditions. Maximum sorption was found to occur at pH 3.0 for all the metal ions studied. Results showed that metallic ion uptake by the blended membrane declined with increase in ionic strength. This trend was also observed at an increased temperature of 50ºC for Pb2+, Cu2+ and 40ºC for Zn2+. Increase in initial metal ion concentration led to increase in metal ion uptake. At the end of the chemical remediation, the blended membrane was found to be effective to some extent, with the reaction being exothermic.

scholarly journals Sorption Analysis of 137Cs On Karawang’s Clay Samples

2016 ◽  
Vol 5 (3) ◽  
Author(s):  
Budi Setiawan ◽  
Suci Prihastuti ◽  
Setyo S. Moersidik
Keyword(s):  
Ionic Strength ◽  
Radioactive Waste ◽  
Waste Disposal ◽  
Contact Time ◽  
Freundlich Isotherm ◽  
Radioactive Waste Disposal ◽  
Order Kinetic ◽  
Disposal Facility ◽  
Kd Values ◽  
Assessment Activity

The objective of this work is to characterize the specific of distribution coefficient (Kd) values of 137Cs onto Karawang’s clay for radioactive waste disposal facility purpose. Sorption phenomena was affected by contact time, ionic strength and loaded concentration of CsCl.  Experiments were done in a batch method, with initial concentration was 10-8 M CsCl in the experiments of contact time and ionic strength effects. In the CsCl loading experiment, the concentration was varied from 10-8 to 10-4 M CsCl and 137Cs radioactive solution was used as a tracer. The solid-liquid ratio is 10-2 g/mL.  The results shown that obtained Kd values were 21,714 and 4035 mL/g after contacted for 8 days for Sample-1 and 2, respectively. The presence of K+ and Na+ ions in solution had reduced the Kd value Cs-137 where the effect of K+ is greater than Na+ on decreased the value of Kd.  The increasing of CsCl concentrations in solution had reduced the value of Kd.  In both samples of clay were closely fit to Freundlich isotherm and pseudo-second order kinetic model.  The results are very useful as the input of the safety assessment activity of site candidate for radioactive waste disposal facility in the future.

Determination of the complexation properties of a crosslinked poly(acrylic acid) gel with copper(II), nickel(II), and lead(II) in dilute aqueous solution

2001 ◽  
Vol 79 (4) ◽  
pp. 370-376 ◽  
Author(s):  
Catherine Morlay ◽  
Yolande Mouginot ◽  
Monique Cromer ◽  
Olivier Vittori
Keyword(s):  
Aqueous Solution ◽  
Ionic Strength ◽  
Acrylic Acid ◽  
Metal Ion ◽  
Conditional Stability ◽  
Binding Properties ◽  
Complex Species ◽  
Complexing Capacity ◽  
Dilute Aqueous Solution ◽  
Poly Acrylic Acid

The possible removal of copper(II), nickel(II), or lead(II) by an insoluble crosslinked poly(acrylic acid) was investigated in dilute aqueous solution. The binding properties of the polymer were examined at pH = 6.0 or 4.0 with an ionic strength of the medium µ = 0.1 or 1.0 M (NaNO3) using differential pulse polarography as an investigation means. The highest complexing capacity of the polyacid was obtained with lead(II) at pH = 6.0 with µ = 0.1 M, 4.8 mmol Pb(II)/g polymer. The conditional stability constants of the complex species formed were determined using the method proposed by Ruzic assuming that only the 1:1 complex species was formed; for lead(II) at pH = 6.0 and µ = 0.1 M, log K' = 5.3 ± 0.2. It appeared that the binding properties of the polymer increased, depending on the metal ion, in the following order: Ni(II) < Cu(II) < Pb(II). The complexing capacity and log K' values decreased with the pH or with an increase of the ionic strength. These results were in agreement with the conclusions of our previous studies of the hydrosoluble linear analogues. Finally, with the insoluble polymer, the log K' values were comparable to those previously obtained with the linear analogue whereas the complexing capacity values expressed in mmol g-1 were slightly lower.Key words: insoluble crosslinked poly(acrylic acid), copper(II), nickel(II), and lead(II) complexation.

Highly Selective Separation and Enrichment of Phosphopeptides by Uranyl-Salophen Immobilized Silica Gel Material

2015 ◽  
Vol 1095 ◽  
pp. 341-344 ◽  
Author(s):  
Can Hui Xu ◽  
Guang Liang Zhang ◽  
Xin Zhou ◽  
Xi Lin Xiao ◽  
Chang Ming Nie ◽  
...  
Keyword(s):  
Silica Gel ◽  
Metal Ion ◽  
High Selectivity ◽  
Separation Efficiency ◽  
Solid Phase ◽  
Tetradentate Ligand ◽  
Peptide Mixtures ◽  
New Material ◽  
Solid Phase Material

The characterization of phosphoproteins requires highly specific methods for the separation and enrichment of phosphopeptides. Here we report a novel metal ion-immobilized solid phase material for the separation and enrichment of phosphopeptides. The material is uranyl-salophen-silica gel (USSG) particles in which salophen is a tetradentate ligand of uranyl ion. In USSG salophen is connected on the surface of silica gel and uranyl is bound on the surface through its coordination with salophen. Phosphopeptides can be selectively retained by USSG because uranyl-salophen can bind phosphate moiety with strong affinity and high selectivity. The new material USSG has been successfully used for the separation of phosphopeptides from peptide mixtures with the separation efficiency of 97.0% to 97.4%.

Comparison between specific surface complexation and Donnan ion-exchange models for describing the adsorption of cations on kraft fibres – literature evidence and EXAFS study of Cu(II) binding

2010 ◽  
Vol 25 (2) ◽  
pp. 178-184 ◽  
Author(s):  
Ola Sundman ◽  
Per Persson ◽  
Lars-Olof Öhman
Keyword(s):  
Ionic Strength ◽  
Ion Exchange ◽  
Metal Ion ◽  
Experimental Conditions ◽  
Cellulose Fibres ◽  
Metal Ion Adsorption ◽  
Literature Evidence ◽  
Trivalent Cations ◽  
Exafs Study ◽  
Low Ionic Strength

Abstract A compilation of the applied experimental conditions when studying metal ion adsorption onto kraft fibres, and the resulting conclusion, revealed that the ionic strength conditions used during the experiments were an important dividing factor. At low ionic strengths, the conclusion has regularly been that the Donnan ion-exchange model could correctly predict the adsorption while, at higher ionic strengths, it has often been concluded that the formation of specific metal-ion fibre complexes must be assumed. To study this apparent influence from the presence of monovalent sodium ions, Cu K-edge EXAFS spectra of Cu2+ ions adsorbed to kraft fibres were collected in media of “0” to 100 mM NaCl. Combined with previous data, these measurements confirmed that at very low ionic strength, the importance of specific interactions between the chemically modified cellulose fibres and the Cu(II) ions significantly decreased. For a detailed description of the adsorption phenomenon, both types of interactions must be considered simultaneously. For most technical and engineering applications, however, the Donnan model can be used at low ionic strength conditions, i.e. I ≲ 10 mM. At higher ionic strengths, though, the inclusion of specific complexes in the model is necessary for correctly describing the adsorption of di- and trivalent cations with strong complex forming properties.

scholarly journals Metal–Organic Frameworks as Key Materials for Solid-Phase Microextraction Devices—A Review

Separations ◽  
2019 ◽  
Vol 6 (4) ◽  
pp. 47 ◽  
Author(s):  
Gutiérrez-Serpa ◽  
Pacheco-Fernández ◽  
Pasán ◽  
Pino
Keyword(s):  
Metal Ion ◽  
Solid Phase Microextraction ◽  
Metal Clusters ◽  
Solid Phase ◽  
Metal Organic Frameworks ◽  
High Chemical ◽  
Current State ◽  
Metal Organic ◽  
Sorbent Materials ◽  
Ordered Porous

Metal–organic frameworks (MOFs) have attracted recently considerable attention in analytical sample preparation, particularly when used as novel sorbent materials in solid-phase microextraction (SPME). MOFs are highly ordered porous crystalline structures, full of cavities. They are formed by inorganic centers (metal ion atoms or metal clusters) and organic linkers connected by covalent coordination bonds. Depending on the ratio of such precursors and the synthetic conditions, the characteristics of the resulting MOF vary significantly, thus drifting into a countless number of interesting materials with unique properties. Among astonishing features of MOFs, their high chemical and thermal stability, easy tuneability, simple synthesis, and impressive surface area (which is the highest known), are the most attractive characteristics that makes them outstanding materials in SPME. This review offers an overview on the current state of the use of MOFs in different SPME configurations, in all cases covering extraction devices coated with (or incorporating) MOFs, with particular emphases in their preparation.

scholarly journals Polyamine-Based Organo-Clays for Polluted Water Treatment: Effect of Polyamine Structure and Content

Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 897 ◽  
Author(s):  
Cinzia Cristiani ◽  
Elena Maria Iannicelli-Zubiani ◽  
Giovanni Dotelli ◽  
Elisabetta Finocchio ◽  
Paola Gallo Stampino ◽  
...  
Keyword(s):  
Hybrid Materials ◽  
Environmental Remediation ◽  
Metal Ion ◽  
Solid Phase ◽  
Nir Spectroscopy ◽  
Linear Structure ◽  
Polluted Water ◽  
Amino Groups ◽  
Metal Ion Removal ◽  
Clay Matrix

Hybrid materials based on clays and polyamines are supposed to be efficient heavy metals sorbents due to the well-known adsorption behaviour of the clay matrix and to the coordination properties of un-protonated amino groups. For this purpose, a montmorillonite clay was modified with three different aliphatic polyamines: L6 and L10 have a linear structure with six and ten amino groups, respectively, while B14 is a branched polyamine with fourteen amino groups. Initial amine concentration was the main parameter investigated and data were fitted with Langmuir and Freundlich models. Interaction mechanisms between clay and amines were deeply investigated by different experimental techniques such as X-ray powder diffraction (XRD), thermal analysis measurements (DTG), Fourier Transform Infrared Spectroscopy (FT-IR) and diffuse reflectance (NIR) spectroscopy. Experimental results showed that the amount of amines efficiently immobilized in the solid phase can be increased by increasing the initial concentration of polyamines in the clay modification process. These data were best fitted by Freundlich model, indicating a presence of surface sites of different nature. In the resulting hybrid materials, neither the accessibility of the NH/NH2 groups of the amines, nor the accessibility of the structural OH of the clay was hindered. Several preliminary tests in La ions’ uptake and release from aqueous solution were also carried out. In the conditions used for this study, total metal ion removal was achieved at sufficiently low linear amine loadings (i.e., 0.45 mmol/gclay for the small L6 amine), suggesting that these hybrid materials are promising for the proposed application in environmental remediation.

An Experimental Approach on the Effect of Rock Alteration on Sorption Behavior

2006 ◽  
Vol 932 ◽  
Author(s):  
Yuichi Niibori ◽  
Yasunori Kasuga ◽  
Hiroaki Yoshikawa ◽  
Kouichi Tanaka ◽  
Osamu Tochiyama ◽  
...  
Keyword(s):  
Silicic Acid ◽  
Experimental Approach ◽  
Solid Phase ◽  
Sorption Behavior ◽  
Flow Paths ◽  
Geological Disposal ◽  
Long Time ◽  
Degree Of Crystallization ◽  
Rock Alteration ◽  
Alkaline Groundwater

ABSTRACTIn the geological disposal of radioactive wastes, cement used for the repository construction alters the condition of groundwater to highly alkaline of pH about 13. Such alkaline groundwater around the repository would alter the surfaces of the rocks in the flow paths to the amorphous phase. Once the surface is altered, it takes a geological period (so much long time) to restore the surface to its former condition. This study examined the sorption behavior of europium (Eu-152 (tracer), Eu-151 (5×10-5 M, carrier) onto some silica minerals with polymeric silicic acid. Polymeric silicic acid also affects the alteration of the solid surface.The results showed that the kinds of silica minerals strongly affect the sorption behavior in the range of 5<pH<8. The main difference was due to the degree of crystallization of the solid phase, the specific surface area and the concentration of polymeric silicic acid. Since the amorphous silica or polymeric silicic acid takes a loose structure, the isoelectric point is high compared to the crystal ones such as opal-CT and cristobalite, which in turn decreases the sorption. The crystalline silica with polymeric silicic acid remarkably decreased the sorption of europium. This suggested that the surface of solid phase was altered by polymeric silicic acid.

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