Removal of uranium(VI) from aqueous solutions and nuclear industry effluents using humic acid-immobilized zirconium-pillared clay

Removal of uranium [U(VI)] from aqueous solutions with humic acid-immobilized zirconium-pillared clay (HA-Zr-PILC) was investigated using a batch adsorption technique. The adsorbent was characterized using XRD, FTIR, SEM, TG/DTG, surface area analyzer and potentiometric titration. The effects of pH, contact time, initial concentration, adsorbent dose, and adsorption isotherm on the removal process were evaluated. A maximum removal of 97.6 ± 2.1 and 94.7 ± 3.3% was observed for an initial concentration of 50 and 100 mg L⁻¹, respectively at pH 6.0 and an adsorbent dose of 2.0 g L⁻¹. Equilibrium was achieved in approximately 180 min. The mechanism for the removal of U(VI) ions by HA-Zr-PILC was based on an ion exchange reaction. The experimental kinetic and isotherm data were analyzed using a second-order kinetic equation and Langmuir isotherm model, respectively. The monolayer adsorption capacity for U(VI) removal was found to be 132.68 ± 5.04 mg g⁻¹. An increase of temperature of the medium caused an increase in metal adsorption. Complete removal (≅100%) of U(VI) from 1.0 L of a simulated nuclear industry effluent sample containing 10.0 mg U(VI) ions was possible with 1.5 g of HA-Zr-PILC. The adsorbent was suitable for repeated use (over 4 cycles) without any noticeable loss of capacity.     

Removal of uranium (VI) from aqueous solution by adsorption of hematite

Hematite, a type of inorganic-sorptive medium, was used for the removal of U (VI) from aqueous solutions. Variables of the batch experiments including solution pH, contact time, initial concentration, temperature, calcium and magnesium ions were studied. The results indicated that the adsorption capacities are strongly affected by the solution pH, contact time and initial concentration. A higher pH favors higher U (VI) removal. The adsorption was also affected by temperature and calcium and magnesium ions, but the effect is very weak. The maximum adsorption capacity (q_m) only increased from 3.36 mg g⁻¹ to 3.54 mg g⁻¹ when the temperature was increased from 293 K to 318 K. A two-stage kinetic behavior was observed in the adsorption of uranium (VI): very rapid initial adsorption in a few minutes, followed by a long period of slower uptake. It was found that an increase in temperature resulted in a higher uranium (VI) loading per unit weight of the sorbent. The adsorption of uranium by hematite had good efficiency, and the equilibrium time of adsorbing uranium (VI) was about 6 h. The isothermal data were fitted with both Langmuir and Freundlich equations, but the data fitted the former better than the latter. The pseudo-first-order kinetic model, pseudo-second-order kinetic model and intraparticle diffusion model were used to describe the kinetic data, but the pseudo-second-order kinetic model was the best. The thermodynamic parameter ΔG⁰ were calculated, the negative ΔG⁰ values of uranium (VI) at different temperatures confirmed the adsorption processes were spontaneous.     

Phosphate removal by activated carbon–silica nanoparticles composite,kaolin, and olive cake

This work aimed to utilize four low-cost materials, namely activated carbon (AC), activated carbon–nanoparticle composite, kaolin, and olive cake, for phosphate removal. Batch mode tests were used to evaluate the performance of the adsorbents. The parameters affecting the adsorption process such as pH, initial concentration, mixing time, dosage, and temperature were studied. The obtained results showed that the removal efficiency of the adsorbents followed the order of: activated carbon–nanosilica > activated carbon > kaolin > olive cake. The addition of silica nanoparticles significantly enhanced the removal efficiency of activated carbon by 18.1% reaching a removal efficiency of 98% at 15wt% nanosilica loading. The adsorption isotherm data fitted well with Langmuir and Redlich–Peterson models with a correlation coefficient of >0.98, which indicates a monolayer homogenous adsorption. The fitness of the kinetic models was ranked as: pseudo-second-order > pseudo-first-order > intraparticle model. The calculated values of ΔH° = 23.4 kJ/mole, ΔS° = 0.11 kJ/mole, and ΔG = ?7.4 to ?11.8 kJ/mole indicated the endothermic and spontaneous nature of adsorption. The positive value of activation energy (17.66 kJ/mole) and the very low value of the sticking probability (2.4 × 10^?4) suggest high indefinite sticking of the phosphate ions to the adsorbent surface. The removal efficiency increased with time, dosage, and temperature, while it decreased with the increase in the initial concentration at an optimum pH of 7. The obtained results buttressed the benefit of using silica nanoparticles to enhance activated carbon capacity for phosphate removal, while kaolin and olive cake provided lower removal.     

Combating dye pollution using cocoa pod husks: a sustainable approach

The adsorptive potential of activated carbon prepared by chemical activation of Cocoa pod husk (CPHAA) to remove Congo red (CR) dye from its aqueous solution was investigated in this study. CPHAA was characterised using Energy Dispersive X-Ray, Scanning Electron Micrograph and Fourier Transform Infrared Spectroscopy techniques. The effects of contact time, initial dye concentration, pH and solution temperature were studied. Equilibrium data were fitted to Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherm models. The equilibrium data were best represented by Langmuir isotherm model, with maximum monolayer adsorption capacity of 43.67 mg/g. The kinetic data were fitted to Pseudo-first-order, Pseudo-second-order, Elovich and Intraparticle diffusion models; the pseudo-second-order kinetic model provided the best correlation. Thermodynamic parameters such as standard enthalpy (ΔH^o), standard entropy (ΔS^o) and standard free energy (ΔG^o) were evaluated. The thermodynamic study showed that the process is endothermic, spontaneous and feasible. The mean free energy of adsorption shows that the mechanism is by physisorption. CPHAA was found to be an effective adsorbent for the removal of CR dye from aqueous solution.     

Behavior and analysis of Cesium adsorption on montmorillonite mineral

The adsorption of Cs by montmorillonite and the effects of experimental conditions on adsorption were investigated by using ¹³⁴Cs as a radioactive tracer. Additionally, the Cs-adsorbed and the modified montmorillonite were analyzed by X-ray Diffractometer System (XRD) and Scanning Electron Microscopy (SEM). The results showed that the adsorption of Cs by montmorillonite was efficient in the initial concentration (C₀) of 30 μg/L Cs nitrate solution with 20 g/L montmorillonite at room temperature. In this condition, more than 98% Cs⁺ ions could be adsorbed at pH 8. The adsorption equilibrium was achieved within 5 min and the relationship between the concentration of Cs⁺ in aqueous solutions and adsorption capacities of Cs⁺ can be described by the Langmuir adsorption isotherm. The adsorption rate would decrease when temperature increase from 0 °C to 50 °C or in presence of coexistent K⁺, Na⁺ and Ca²⁺, while modification by (NH₄)₂SO₄, [Ag(NH₃)₂]⁺, [Cu(NH₃)₄]²⁺ or 450 °C could improve the adsorption abilities of montmorillonite for Cs⁺. However, more than 89% of adsorbed Cs⁺ on montmorillonite could be desorbed by 2 mol/L HNO₃ solutions. The XRD and SEM analysis further showed that the structure of the Cs-adsorbed or modified montmorillonite were different from that of the original one.     

Improved performance of a biomaterial-based cation exchanger for the adsorption of uranium(VI) from water and nuclear industry wastewater

The amine-modified polyhydroxyethylmethacrylate (poly(HEMA))-grafted biomaterial (tamarind fruit shell, TFS) carrying carboxyl functional groups at the chain end (PGTFS-COOH) was prepared and used as an adsorbent for the removal of uranium(VI) from water and nuclear industry wastewater. FTIR spectral analysis revealed that U(VI) ions and PGTFS-COOH formed a chelate complex. The adsorption process was relatively fast, requiring only 120 min to attain equilibrium. The adsorption kinetic data were best described by the pseudo-second-order equation. The equilibrium adsorption data were correlated with the Sips isotherm model. The maximum U(VI) ions uptake with PGTFS-COOH was estimated to be 100.79 mg/g. The complete removal of 10 mg/L U(VI) from simulated nuclear industry wastewater was achieved by 3.5 g/L PGTFS-COOH. The reusability of the adsorbent was demonstrated over 4 cycles using NaCl (1.0 M) + HCl (0.5 M) solution mixture to de-extract the U(VI). The results show that the PGTFS-COOH tested is very promising for the recovery of U(VI) from water and wastewater.     

Study of Ni adsorption on NKF-6 zeolite

The adsorption of ⁶³Ni from aqueous solutions using NKF-6 zeolite was investigated by a batch technique under ambient conditions. The adsorption was investigated as a function of contact time, pH, ionic strength, foreign ions, humic substances (FA/HA) and temperature. The kinetic adsorption was well described by the pseudo-second-order rate equation. The adsorption of ⁶³Ni on NKF-6 zeolite was strongly dependent on pH and ionic strength, and the adsorption of ⁶³Ni increased with increasing NKF-6 zeolite content. At low pH values, the presence of FA enhanced the adsorption of ⁶³Ni on NKF-6 zeolite, but the presence of HA had no drastic effect. At high pH values, the presence of FA or HA decreased the adsorption of ⁶³Ni on NKF-6 zeolite. The adsorption isotherms were well represented by the Langmuir model. The thermodynamic parameters (i.e., ΔH⁰, ΔS⁰and ΔG⁰) for the adsorption of ⁶³Ni were determined from the temperature dependent isotherms at 293.15, 313.15 and 333.15 °K, respectively, and the results indicate that the adsorption reaction was favored at high temperature. The results suggest that the adsorption process of ⁶³Ni on NKF-6 zeolite is spontaneous and endothermic.     

Taxonomy of groundwater quality using multivariate and spatial analyses in the Tuticorin District,Tamil Nadu,India

A holistic appraisal of the quality of groundwater from the Tuticorin District has been conducted using multivariate statistical and spatial analyses. The objectives of the study were to delineate the spatial and temporal variabilities in groundwater quality and to understand its suitability for human uses. A total of 100 groundwater samples were collected and analyzed for major cations and anions during pre-monsoon and post-monsoon. Water quality index rating was calculated to quantify overall water quality for human consumption. The PRM samples exhibit poor quality in greater percentage when compared with POM due to the dilution after rainfall. Correlation, factor analysis, and plot of the factor scores reflect the seawater intrusion and weathering process. The mineral stability diagrams indicated that the groundwater is in equilibrium with kaolinite and Ca-montmorillonite, whereas Gibbs plot showed that the chemical composition of groundwater in both districts is controlled by the natural weathering processes irrespective of seasons. The major water type identified in this study is the Ca²⁺–Mg²⁺–HCO₃ ^? type, which degrades into predominantly Na⁺–Cl^?–SO₄ ^2? more saline groundwater toward the coast.     

An interlaboratory comparison of nanosilver characterisation and hazard identification: Harmonising techniques for high quality data

Within the FP7 EU project NanoValid a consortium of six partners jointly investigated the hazard of silver nanoparticles (AgNPs) paying special attention to methodical aspects that are important for providing high-quality ecotoxicity data. Laboratories were supplied with the same original stock dispersion of AgNPs. All partners applied a harmonised procedure for storage and preparation of toxicity test suspensions. Altogether ten different toxicity assays with a range of environmentally relevant test species from different trophic levels were conducted in parallel to AgNP characterisation in the respective test media. The paper presents a comprehensive dataset of toxicity values and AgNP characteristics like hydrodynamic sizes of AgNP agglomerates and the share (%) of Ag⁺-species (the concentration of Ag⁺-species in relation to the total measured concentration of Ag). The studied AgNP preparation (20.4 ± 6.8 nm primary size, mean total Ag concentration 41.14 mg/L, 46–68% of soluble Ag⁺-species in stock, 123.8 ± 12.2 nm mean z-average value in dH₂O) showed extreme toxicity to crustaceans Daphnia magna, algae Pseudokirchneriella subcapitata and zebrafish Danio rerio embryos (EC50 < 0.01 mg total Ag/L), was very toxic in the in vitro assay with rainbow trout Oncorhynchus mykiss gut cells (EC50: 0.01–1 mg total Ag/L); toxic to bacteria Vibrio fischeri, protozoa Tetrahymena thermophila (EC50: 1–10 mg total Ag/L) and harmful to marine crustaceans Artemia franciscana (EC50: 10–100 mg total Ag/L). Along with AgNPs, also the toxicity of AgNO₃ was analyzed. The toxicity data revealed the same hazard ranking for AgNPs and AgNO₃ (i.e. the EC50 values were in the same order of magnitude) proving the importance of soluble Ag⁺-species analysis for predicting the hazard of AgNPs. The study clearly points to the need for harmonised procedures for the characterisation of NMs. Harmonised procedures should consider: (i) measuring the AgNP properties like hydrodynamic size and metal ions species in each toxicity test medium at a range of concentrations, and (ii) including soluble metal salt control both in toxicity testing as well as in Ag⁺-species measurements. The present study is among the first nanomaterial interlaboratory comparison studies with the aim to improve the hazard identification testing protocols.     

Chemisorption and Physical Adsorption Roles in Cadmium Biosorption by Chlamydomonas Reinhardtii

Abstract

The aim of this study was to investigate the mechanism of cadmium (Cd) adsorbed by microalgae Chlamydomonas reinhardtii (C.reinhardtii). The kinetic and adsorption isotherm of the process could be well described by mathematical models. Chemical modification experiments and Fourier transform infrared spectra indicated that carboxyl and amine groups were the important functional groups for adsorption of Cd. The maximum contribution of physical adsorption in the overall adsorption process was evaluated as 5.5%. These results indicated that chemisorption was the dominating mechanism of Cd biosorption by C.reinhardtii.     

Americium adsorption on the surface of macrophytic algae

Data are presented on the rates at which americium (Am) deposits upon blade surfaces of three benthic algal species (Ulva rigida, Fucus vesiculosus and Gigartina stellata) following short-term exposures (1–6 h). Am is taken up in direct proportion to the ambient radionuclide concentration in sea water. Uptake by the green alga was 3 to 5 times greater than that for the brown and red species. Experimental evidence indicated that Am accumulation is a passive process and that adsorption takes place mainly on the thin outer organic coating of the seaweed. The Am transport coefficients (0·9–4·1 × 10?⁵ Bq cm?² s?¹ per Bq ml?¹ sea water) are quite similar to that previously found for the naturally occurring α-emitter ²¹⁰Po, but are an order of magnitude lower than a plutonium transport coefficient reported in the literature. Release of labelled extracellular products associated with the algal surface coating is considered to be responsible for the rapid loss of Am observed previously in macroalgae and may in fact serve as a mechanism for transferring Am to filter feeding zooplankton.     

Assessment of El-Salaam underground water for poultry use

Water quality for 13 wells in El-Salaam, in a new city near Cairo, has been investigated. Those wells were dug specifically to provide water for a company specializing in broiler poultry production. The water was analyzed for the following bacteriological parameters: total bacterial counts (10²–10⁴), total coliforms (<1?10²), fecal coliforms (<1?10²) fecal streptococci (<1?10³), aerobic spore formers (10²–10⁴) and total counts for Clostridia (<1?10³) per 100 mL. Chemical parameters such as pH, sulphate, alkalinity, hardness, and pesticides indicate that the water is unacceptable for poultry production. This study illustrates the need for monitoring and maintaining the integrity of groundwater sources at El-Salaam.     

Genetic differentiation of black saxaul, Haloxylon aphyllum (Chenopodiaceae), along a soil salinity gradient in the Kyzylkum Desert

Populations of Haloxylon àphyllum in the Kyzylkum Desert have been found to be markedly deficient in heterozygotes at a medium level of genetic diversity (P ₉₅ = 0.56, A = 1.67, H _o = 0.14, H _e = 0.28). Spatial genetic differentiation of these populations have been revealed along a soil salinity gradient (from 0 to 0.5 mmol Na⁺/g), with their genetic diversity reaching a maximum (H _o = 0.21?C0.25, H _e = 0.25?C0.27) in areas with a moderate salinity level (0.05?C0.1 mmol Na⁺/g). Locus Got-2 can serve as a marker of this differentiation (Fst_Got-2 = 0.4).     

Influence of Operating Conditions on the Removal Cd Ions from Aqueous Media by Adsorption Using Chlamydomonas Reinhardtii

Chlamydomonas reinhardtii(C.reinhardtii)was used to study adsorption of cadmium(Cd)from aqueous media within various experimental conditions.Results showed that the adsorption process was very fast,with most of the adsorption occurring within30 min of contact time and the equilibrium state was reached in about 60 min.The adsorption ability of the algae increases with the increasing adsorptions sites on cells.Maximum adsorption was observed at the initial Cd concentration of 100 mg/L and pH 6.0.The adsorption was markedly inhibited in the presence of calcium and magnesium ions at 10 mM and the Cd removal efficiency was reduced by 16.54% and 14.99% respectively.This study would be a finding of note with regard to practical wastewater treatment.     

Heavy metal pollution abatement using rock phosphate mineral

The low-grade rock phosphate of Jhabua, Madhya Pradesh (India), was investigated for its possible application in the removal of lead, copper, zinc and cobalt ions from aqueous solutions. Effects of contact time, amount of adsorbent and initial concentration of metal ions were studied. Adsorption of heavy metal ions was found to follow the order: Pb2+ > Cu2+ > Zn2+ > Co2+. The probable mechanism of metal ions removal by rock phosphate was found to be by its dissolutions followed by subsequent precipitation.     

Biosorption of uranium (VI) by immobilized Aspergillus fumigatus beads

Biosorption of uranium (VI) ions by immobilized Aspergillus fumigatus beads was investigated in a batch system. The influences of solution pH, biosorbent dose, U (VI) concentration, and contact time on U (VI) biosorption were studied. The results indicated that the adsorption capacity was strongly affected by the solution pH, the biosorbent dose and initial U (VI) concentration. Optimum biosorption was observed at pH 5.0, biosrobent dose (w/v) 2.5%, initial U (VI) concentration 60 mg L⁻¹. Biosorption equilibrium was established in 120 min. The adsorption process conformed to the Freunlich and Temkin isothermal adsorption models. The dynamic adsorption model conformed to pseudo-second order model.     

Mutagenicity of atmospheric air and snow cover in the city of Syktyvkar estimated by the somatic mutation test inTradescantia (Clone 02) stamen hairs

Genotoxicity of atmospheric air was studied in Syktyvkar for three years (1995–1997) using the test of somatic mutations inTradescantia (clone 02) stamen hairs. The data obtained indicate local air pollution in the city. The tested samples of snowmelt, where Ni⁺ and Zn²⁺ ions were the main pollutants, had a high teratogenic effect on stamen hairs. The somatic mutation rate similar to that in the control group was obtained in the experiment with only one sample, in which the total content of metal ions was the lowest.     

Geochemical associations of plutonium and γ-emitting radionuclides in caithness soils and marine particulates

Geochemical associations of plutonium and artificial γ-emitting radionuclides have been investigated in soils and marine particulate material from the immediate vicinity of the Dounreay Nuclear Power Development Establishment (DNPDE) Caithness. The artificial radionuclides present in these materials arise from a variety of sources: world-wide nuclear weapons test fallout, direct deposition from atmospheric discharges at DNPD, and the return to land of activity previously discharged to sea (containing contributions from Dounreay and Sellafield). The levels, although sufficient to permit satisfactorily low counting errors, are of negligible radiological significance, the plutonium being more than 1000 times less than the NRPB Generalised Derived Limit (GDL) for well-mixed soil. Sequential leaching using selective extractants was performed to quantify the percentages of each nuclide in the following notional fractions: (a) readily available, (b) exchangeable and bound at specific adsorption sites, (c) chelated as insoluble organic complexes, (d) associated with sesquioxides, and (e) residual. Plutonium was found to be associated mainly with phases (c) and (d), while the γ-emitters present in the marine particulate material showed quite varied distributions. The degree of chemical fixation in the particulates follows the sequence ⁴⁰K¹³⁷Cs¹⁰⁶Ru¹²⁵Sb^239,240Pu¹⁴⁴Ce⁶⁰Co^154,155Eu.     

Cleaning the river Damodar (India): impact of COVID-19 lockdown on water quality and future rejuvenation strategies

Globally, it is established that the partial lockdown system assists to improve the health of the total environment due to inadequate anthropogenic actions in different economic sectors. The ample research on fitness of environment has been proved that the strict imposition of lockdown was the blessings of environment. The river Damodar has historical significance and lifeline for huge population of Jharkhand and West Bengal state of India but in the recent years the water quality has been deteriorated due to untreated industrial effluents and urban sewage. The main objective of this study is to examine the water quality of river Damodar during and prelockdown phase for domestic use and restoration of river ecosystem. A total of eleven (11) effluent discharge sites were selected in prelockdown and during lockdown phase. A new approach of water quality assessment, i.e., water pollution index (WPI) has been applied in this study. WPI is weightage free, unbiased method to analysis of water quality. The result shows that the physical, chemical and heavy elements were found beyond the standard limit in prelockdown period. The cation and anion were arranged in an order of Na²⁺ ?>?K⁺ ?>?Ca²⁺ ?>?Mg²⁺ and Cl^??>?So₄^??>?No₃^??>?F^? in both the sessions. WPI of prelockdown showed that about 100% water samples are of highly polluted. WPI of lockdown period showed that around 90.90% samples improved to ‘good quality’ and 9.10% of samples are of ‘moderately polluted.’ Hypothesis testing by ‘t’ test proved that there was a significant difference (ρ?=?0.05%) in values of each parameter between two periods. Null hypothesis was rejected and indicated the improvement of river water quality statistically. Spatial mapping using Arc GIS 10.4 interpolation (IDW) helps to understand spatial intensity of pollution load in two periods. This research study should be helpful for further management and spatial diagnosis of water resource of river Damodar.

     

The performance of solar powered desiccant dehumidifier in India: an experimental investigation

The regeneration and adsorption of desiccant wheel for producing the dry air was experimentally investigated. The air needed for regeneration was heated in an evacuated tube solar collector with surface area 4.44 m². The desiccant wheel is regenerated at the temperature in the range of 43.9–72.6°C. The regeneration and adsorption performances are affected by the regeneration temperature, wheel rotation, air flow rate (process and regeneration) and ambient conditions. By comparing the adsorption and regeneration performance at different air flow rate and constant rph, it was found that maximum adsorption and regeneration rates are obtained at air flow rate of 210.789 kg/h. Regeneration temperature directly affects the effectiveness of the desiccant wheel. Maximum desiccant wheel effectiveness of regeneration sector and adsorption sector is obtained at air flow rate of 105.394 kg/h. The regeneration performance of desiccant wheel with evacuated tube solar air collector is suitable for the Indian climate.