Highly efficient adsorption of uranyl ions using hydroxamic acid-functionalized graphene oxide

A chelating matrix prepared by immobilizing N-hydroxyl amine onto graphene oxide functionalized with aspartic acid (GO-HDX) was applied to recover UO2 2+ from their SO4 2− leach liquor. SEM-EDAX, FT-IR, TGA, and XRD instruments, in addition, Raman spectroscopy (IR-Raman), were used to analyze the synthesized GO-HDX. The static extraction technique optimized various physicochemical parameters that impacted the UO2 2+ extraction. The optimal pH, time of contact, initial concentration, GO-HDX dose, temp., foreign ions, and eluting agents were gained. The experimental equilibrium documents were assessed using Langmuir and Freundlich equations. The Langmuir equation model quite fits the investigational adsorption data with a maximum uptake of 277.78 mg/g, and it implied the attending of monolayer coverage of adsorbed molecules. Pseudo-first- and pseudo-second-order analyses were done to inspect the kinetic results. The data indicated that pseudo-second-order kinetics fit all concentrations. The intended thermodynamic factors were ∆G° negative values and ∆H° positive value. The data signified that the UO2 2+ extraction onto GO-HDX was spontaneous adsorption and endothermic at higher temperatures. The regeneration efficiency of GO-HDX was 98% using 1 M HCl.

DE Fluoridation of Domestic Waste Water by using Activated Diatomaceous Earth in fixed Mattress Column Adsorption System

Study aims to eliminate fluoride from treated waste water or ground water through adsorption technique by using Activated Diatomaceous Earth as a sorbent. Study found that there is no change in pH and TDS, but the concentration of Fluoride ions reduced. The most elimination potential of 71.97 mg/kg turned into achieved for activated diatomaceous earth with particle sizes of 0.075-0.425 mm. The absorbance capability of diatomaceous earth (DE) is 20.73% when used as a filtration media. In this analysis, activated diatomaceous earth was used as an adsorbent in a fixed-mattress column adsorption system for DE fluoridation of water. The XRD, BET surface area, FTIR, XRF, Scanning Electron Microscopy (SEM), and pH Point of Zero Charges (pHPZC) evaluation had been executed for adsorbent to explain the mechanisms of absorption and fluoride elimination. The Bradley equation was used to calculate the isothermal data and adsorbent dose. The statistical analyses were performed using Langmuir and Freundlich equations.

Glauconite as a sorbent of 4-nitrophenol

The sorption properties of glauconite from Beloozersk deposits (Saratov region) for 4-nitrophenol (4-NF) have been investigated. The effect of glauconite on pH and 4-nitrophenol structure in solution is estimated. It is shown that glauconite increases pH of aqueous environment to 8 and shifts the equilibrium towards the formation of aci-form 4-NF. The conditions of sorption 4-NF by glauconite are established: the sorption time 20 min, the mass of the sorbent (0.50–1.0) g. The isotherm of sorption by 4-NF glauconite has been obtained; its interpretation is given using the Langmuir and Freundlich equations. The main quantitative sorption characteristics of glauconite such as recovery (R = 64%), distribution coefficient (D = 88) and the Langmuir and Freundlich constants for 4-nitrophenol are calculated. These experiments indicate the potential use of the glauconite from Beloozersk deposits (Saratov region) for 4-NP from various waters.

Synthesis Fe3O4/Talc nanocomposite by coprecipition-ultrasonication method and advances in hexavalent chromium removal from aqueous solution

The Fe3O4/Talc nanocomposite was synthesized by the coprecipitation-ultrasonication method. The reaction was carried out under a inert gas environment. The nanoparticles were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), fourier-transform infrared spectroscopy (FT-IR) and vibrating sample magnetometry techniques (VSM), the surface area of the nanoparticles was determined to be 77.92 m2/g by Brunauer-Emmett-Teller method (BET). The kinetic data showed that the adsorption process fitted with the pseudo-second order model. Batch experiments were carried out to determine the adsorption kinetics and mechanisms of Cr(VI) by Fe3O4/Talc nanocomposite. The adsorption process was found to be highly pH-dependent, which made the material selectively adsorb these metals from aqueous solution. The isotherms of adsorption were also studied using Langmuir and Freundlich equations in linear forms. It is found that the Langmuir equation showed better linear correlation with the experimental data than the Freundlich. The thermodynamics of Cr(VI) adsorption onto the Fe3O4/Talc nanocomposite indicated that the adsorption was exothermic. The reusability study has proven that Fe3O4/Talc nanocomposite can be employed as a low-cost and easy to separate.

Zinc Adsorption in Relation to Soil Properties, Analysed with Langmuir and Freundlich Models in Soils of Kashmir Valley

The phenomenon of fixation of added zinc in soils considerably affects the availability and efficiency of applied zinc. Pertaining to this situation, different land-use soil samples across the valley were analysed for various physico-chemical properties and adsorption capacities. The results showed that the soils were slightly acidic to alkaline in reaction and differ far and wide in other soil properties. Cation exchange capacity (CEC) of the soils showed little variation between the samples and varied from13.3 to 17.2 cmol(p+) kg-1 with an average value of 15.1 cmol(p+) kg-1of soil. The maximum of zinc adsorption were greatly influenced by soil organic matter, clay content and CEC of the soils. The data was fitted to Langmuir and Freundlich equations and the results yielded that the Freundlich equation showed better fit to the sorption data at higher zinc concentrations. However, both the models were having satisfactory results for the obtained data.

Phosphate sorption indices as affected by the calcareousness of soils

An experiment was carried out to study the effects of calcareousness on phosphate sorption indices of soils using three representative calcareous soils, namely Sara (Aquic Eutrochrept), Gopalpur (Aquic Eutrochrept), and Ishurdi (Aeric Haplaquept) series of Bangladesh. Three non-calcareous soils, namely Belabo (Typic dystrudepts), Sonatala (Aeric Endoaquepts) and Ghatail (Aeric Haplaquept) series were also selected for comparison purposes. Phosphate sorption indices of soils were calculated using Langmuir and Freundlich isotherms. Isotherms were constructed taking one gram of air-dried sieved (< 2 mm) soil into a 50 ml centrifuge tube, and subsequently adding seven initial P concentrations, namely 0, 1, 10, 25, 50, 100 and 150 μg/ml to each centrifuge tube employing a soil/solution ratio of 1 : 20 (w/v). According to the Langmuir equation, the amount of phosphate sorbed followed the order: Sonatala > Ghatail > Sara = Gopalpur > Ishurdi > Belabo. The abundance of amorphous iron rather than the calcareousness was putatively responsible for the high phosphate sorption capacity of soils. Maximum phosphorus buffering capacity (MPBC) of the calcareous soils ranged from 33.4 - 62.8 l/kg. Langmuir and Freundlich equations produced different values for soil P requirements (SPR) at 0.2 and 1.0 mg P/l. Calcareous soils would require 27 - 44 mg P/kg soil to attain 0.2 mg P/l soil solution, which is deemed sufficient for crop growth. The soils would require 32 - 58 mg P/kg soil to reach 1.0 mg P/l soil solution, which is regarded to be safe for soils in terms of susceptibility to P losses. The calculated Langmuir constant b values were higher than the threshold value of 0.07 l/mg for two of the calcareous soils. Therefore, even though the non-calcareous soils sorbed more phosphate, higher bonding energy of P sorption for calcareous soils makes them less vulnerable to loss via surface runoff. Dhaka Univ. J. Biol. Sci. 28(1): 93-110, 2019 (January)

Preparation of alkali-activated fly ash-based geopolymer and their application in the adsorption of copper (II) and zinc (II) ions

Alkali activation of fly ash can a promising alternative of the system to improve adsorption capability of fly ash. In finding the best chemical composition of the activator solution, geopolymer has been synthesized using molar ratios of Na2O/SiO2 0.16, 0.3, and 0.5 (Gr1, Gr3, Gr5). The results indicated that the geopolymer synthesized with a ratio molar of Na2O/SiO2 0.3 (Gr3) improved the adsorption properties of fly ash substantially. Gr3 was characterized by BET, XRD, and FTIR. The batch experiment was conducted at the different duration and initial concentrations. The equilibrium sorption data were fitted for the Langmuir and Freundlich equations. The maximum sorption capacities calculated from Langmuir isotherm was 54 mg g-1 and 47 mg g-1 for Cu (II) and Zn (II) respectively. The kinetic data reveal that the pseudo-second order model was appropriate for a description of the kinetic performance.

Phosphorus sorption characteristics of some representative soils of south India

Studies were conducted to investigate P sorption characteristics of representative soils from ten locations of alfisol and ultisol of India using Langmuir and Freundlich equations. The P sorption maxima (b) of soils derived from Langmuir equation in alfisol varied from 520.6 to 574.7 ?g g-1 and ultisol varied from 561.6 to 678.1 ?g g-1. The maximum phosphorus buffering capacity (MPBC) in alfisol ranged from 80.7 to 180.2 ml ?g-1 and ultisol ranged from 162.1 to 284.4 ml ?g-1. Phosphorus sorption maxima was significantly correlated with clay (r2=0.70), Al (r2= 0.73) and Fe (r2=0.81) forms, MPBC (r2=0.67) and Freundlich constants (r2=0.82). The standard P requirement (SPR) to maintain 0.2 mg l-1 P in soil solution for alfisol ranged from 15.62 to 27.62 mg kg-1 and ultisol from 41.98 to 46.35 mg kg-1. The SPR (0.2 mg l-1) was significantly correlated with binding strength coefficient (r2= 0.97) and binding strength coefficient supporting the fact that energy coefficient of a soil is an important index for planning P management strategies. Among the two soil orders in order to maintain optimum P concentration in soil solution for crop growth, ultisol will be required to supply with more P fertilizer as compared to alfisol.SAARC J. Agri., 13(1): 14-26 (2015)

Adsorption Studies of Nickel(II) Metal Ions Uptake Using Fe3O4 Magnetic Nanoadsorbent

In the present study, Fe3O4 magnetic nanoparticles (MNPs) synthesized in-housed using co-precipitation method was applied for the treatment of aqueous solutions contaminated by Ni(II) ions. Experimental results indicated that at 25ºC, the optimum pH value for Ni(II) removal was pH 6.0 and an adsorbent dose of 60.0 mg. The adsorption capacity of Fe3O4 nanoparticles for Ni(II) is 20.54 mg g−1. Adsorption kinetic rates were found to be fast; total equilibrium was achieved after 180 min. Kinetic experimental data fitted very well the pseudo-second order equation and the value of adsorption rate constants was calculated to be 0.004 and 0.0008 g mg−1 min at 5 and 40 mg L−1 initial Ni(II) concentrations, respectively. The equilibrium isotherms were evaluated in terms of maximum adsorption capacity and adsorption affinity by the application of Langmuir and Freundlich equations. The maximum monolayer capacity obtained from the Langmuir isotherm was 24.57 mg g−1 for Ni(II). Results indicate that the Langmuir model fits adsorption isotherm data better than the Freundlich model.

Synthesis and CO2 sorption of silica particles, kinetics and thermodynamics

Spherical ordered mesoporous silica particles with radially oriented mesopores were successfully prepared by using non-ionic amphiphilic di-block co-polymers CnH2n+1-(EO)x-OH as template and tetraorthosilicate (TEOS) as silica precursor. The synthesized mesoporous silica materials were characterized by XRD, N2 adsorption-desorption and SEM techniques. CO2 adsorption at 0 °C was evaluated by a volumetric method, and the CO2 sorption behavior was described by applying both Langmuir and Freundlich equations. Results indicate a high adsorption capacity of CO2 (5-9 mmol/g), depending essentially on the porous texture of the materials. An adsorption kinetic model was proposed to describe the adsorption of CO2 over template-free mesoporous siliceous materials. A good agreement with experimental data was found.