Conductometric and volumetric study of copper sulphate in aqueous ethanol solutions at different temperatures

AbstractAn Anton Par Model 55 densimeter was used to measure the densities of copper sulphate solutions in H2O and EtOH–H2O at 298.15K, 303.15K, 308.15K, and 313.15K. The acquired information was used to ascertain the apparent molar volumes, limiting partial molar volumes, and transfer partial molar volumes of copper sulphate. These computed parameters were utilized to decipher the solute–solute and solute–solvent interactions of copper sulphate in an aqueous ethanol solution. The ion solvation behavior of copper sulphate in water and aqueous ethanol over the range of 298.15–313.15K was studied using the electrical conductivity principle. The Kraus–Bray and Shedlovsky models of conductivity were used to analyze the obtained conductance data. From the obtained data, the limiting molar conductance λ°m, association constant KA, energy of activation of the rating process (Ea), and related thermodynamic parameters were determined. The Walden product (λ°mη0) was determined. The standard thermodynamic parameters of association (ΔG°A, ΔH°A) were calculated and discussed. Increased ion–solvent and solvent–solvent interactions are indicated by limiting molar conductance values with an increasing amount of ethanol. The negative ΔG°A values indicate that the association processes in all of the studied systems are spontaneous processes. The negative estimation of (ΔH°A) demonstrates that the association processes is exothermic in nature

Simultaneous Removal of Calconcarboxylic Acid, NH4+ and PO43− from Pharmaceutical Effluent Using Iron Oxide-Biochar Nanocomposite Loaded with Pseudomonas putida

In the current study, the Fe2O3/biochar nanocomposite was synthesized through a self-assembly method, followed by the immobilization of Pseudomonas putida (P. putida) on its surface to produce the P. putida/Fe2O3/biochar magnetic innovative nanocomposite. The synthesized nanocomposite was characterized using different techniques including X-ray diffraction, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and Fourier-transform infrared spectroscopy (FT-IR). Then, the efficiencies of this material to remove calconcarboxylic acid (CCA) organic dye, ammonium ions (NH4+), and phosphate ions (PO43−) from industrial wastewater were analyzed. The removal rates of up to 82%, 95%, and 85% were achieved for CCA dye, PO43−, NH4+, respectively, by the synthesized composite. Interestingly, even after 5 cycles of reuse, the prepared nanocomposite remains efficient in the removal of pollutants. Therefore, the P. putida/Fe3O4/biochar composite was found to be an actual talented nanocomposite for industrial wastewater bioremediation

The Synthesis of Metal–Organic-Framework-Based Ternary Nanocomposite for the Adsorption of Organic Dyes from Aqueous Solutions

In the present study, a ternary magnetic nanocomposite (SiO2/MnFe2O4/ZIF-8) was synthesized via the embedding of the SiO2/MnFe2O4 nanocomposite within the metal–organic framework (ZIF-8). The synthesized nanocomposite was characterized using suitable techniques including FT-IR, XRD, SEM, TEM, VSM, and BET. The nanocomposite showed a high surface area (SBET = 831 m2·g−1) and superparamagnetic behavior (23.7 emu·g−1). All characterization techniques confirmed the successful combination of three nanocomposite parts (MnFe2O4, SiO2, and ZIF-8). The nanocomposite was examined for the adsorption of organic dyes, malachite green (MG) and methyl red (MR), from aqueous solutions. The adsorption conditions including ionic strength, contact time, pH, and adsorbent dosage were optimized by studying their change effect. The SiO2/MnFe2O4/ZIF-8 nanocomposite showed high adsorption capacities (1000.03 and 1111.12 mg/g) for the removal of MG and MR, respectively, from water. The isotherm and kinetics studies indicated that the adsorption of MG and MR dyes on the surface of the SiO2/MnFe2O4/ZIF-8 nanocomposite followed the Langmuir isotherm model and pseudo-second-order kinetic model, suggesting the monolayer chemisorption mechanism. The reusability study of up to five successive cycles indicated the successful reuse of the SiO2/MnFe2O4/ZIF-8 adsorbent for dye removal from wastewater. The comparison of the present adsorbent to the previously reported adsorbents indicated that it is a promising adsorbent for dye adsorption from wastewater and must be investigated in the future for the removal of additional pollutants

Iron Oxide/Chitosan Magnetic Nanocomposite Immobilized Manganese Peroxidase for Decolorization of Textile Wastewater

Because of its effectiveness in organic pollutant degradation, manganese peroxidase (MnP) enzyme has attracted significant attention in recent years regarding its use for wastewater treatment. Herein, MnP was extracted from Anthracophyllum discolor fungi and immobilized on the surface of magnetic nanocomposite Fe3O4/chitosan. The prepared nanocomposite offered a high surface area for MnP immobilization. The influence of several environmental factors like temperature, pH, as well as storage duration on the activity of the extracted enzyme has been studied. Fourier transmission infrared spectroscopy (FT-IR), scanning electron microscope (SEM), X-ray diffraction (XRD), and transmission electron microscope (TEM) techniques were used for the characterization of the prepared MnP/Fe3O4/chitosan nanocomposite. The efficiencies of the prepared MnP/Fe3O4/chitosan nanocomposite for the elimination of reactive orange 16 (RO 16) and methylene blue (MB) industrial dyes were determined. According to the results, the immobilization of MnP on Fe3O4/chitosan nanocomposite increases its capacity to decolorize MB and RO 16. This nanocomposite allowed the removal of 96% ± 2% and 98% ± 2% of MB and RO 16, respectively. The reusability of the synthesized nanocomposite was studied for five successive cycles showing the ability to retain its efficiency even after five cycles. Thus, the prepared MnP/Fe3O4/chitosan nanocomposite has potential to be a promising material for textile wastewater bioremediation

Effective Heavy Metals Removal from Water Using Nanomaterials: A Review

The discharge of toxic heavy metals including zinc (Zn), nickel (Ni), lead (Pb), copper (Cu), chromium (Cr), and cadmium (Cd) in water above the permissible limits causes high threat to the surrounding environment. Because of their toxicity, heavy metals greatly affect the human health and the environment. Recently, better remediation techniques were offered using the nanotechnology and nanomaterials. The attentions were directed toward cost-effective and new fabricated nanomaterials for the application in water/wastewater remediation, such as zeolite, carbonaceous, polymer based, chitosan, ferrite, magnetic, metal oxide, bimetallic, metallic, etc. This review focused on the synthesis and capacity of various nanoadsorbent materials for the elimination of different toxic ions, with discussion of the effect of their functionalization on the adsorption capacity and separation process. Additionally, the effect of various experimental physicochemical factors on heavy metals adsorption, such as ionic strength, initial ion concentration, temperature, contact time, adsorbent dose, and pH was discussed

Synthesis, Characterization, and Application of Magnetized Lanthanum (III)-Based Metal-Organic Framework for the Organic Dye Removal from Water

A hybrid composite based on metal-organic framework (MOF) was chemically fabricated by embedding the magnetic Fe3O4 nanoparticles within amino-functionalized porous La-MOF (MOF/NH2) to produce a highly efficient and reusable composite of MOF/NH2/Fe3O4. Different proper techniques were used for the characterization of surface morphology and chemical arrangement of the prepared MOF/NH2/Fe3O4 composite. The characterization results using various techniques including Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscope (SEM), Brunauer, Emmett, and Teller analysis (BET), and vibrating sample magnetometer (VSM) approved the successful fabrication of MOF with amino arms on its surface besides the well magnetization using magnetic nanoparticles. The MOF/NH2/Fe3O4 composite showed enhanced adsorption capacity (618 mg/g) toward methyl orange (MO) anionic dye which is higher than many commercial reported adsorbents due to the presence of many types of adsorption sites (NH2 groups and lanthanum sites), large surface area of MOF, and the synergetic effect of magnetic nanoparticles. Moreover, the MOF/NH2/Fe3O4 composite showed selective adsorption of MO dye from dye mixtures owing to the electrostatic attraction. Also, the MOF/NH2/Fe3O4 composite retained over 90% of its efficiency for the dye removal even after six successive cycles. So, the present study provided a practical strategy for the design of functional MOF hybrid composites. Furthermore, due to the adaptability of its architectural form, it is a potential adsorbent material for industrial wastewater treatment uses

Polyethylenimine-Modified Magnetic Chitosan for the Uptake of Arsenic from Water

The removal of heavy metals from water has become a global environmental problem. Various materials have been applied as adsorbent to remove metals from water. In this field, nanomaterials have been gaining increasing interest due to their exceptional properties. In this work, we discuss the synthesis of a core-shell structure nanocomposite by the modification of magnetic chitosan (CS) (Fe3O4/CS) with polyethylenimine (PEI) to produce Fe3O4/CS/PEI composite for the adsorption of arsenic ions (As(V) and As(III)) from aqueous solution. The synthesized materials were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), transmission electron microscope (TEM), and vibrating sample magnetometer (VSM). The results indicated the successful combination of three components of the nanocomposite. The adsorption conditions were optimized by studying the effect of different parameters included pH, contact time, initial concentration, and adsorbent dosage. The optimum adsorption pH was found to be 6.7 while the optimum adsorbent dosage was found to be 2.0 and 1.5 g/L for As(III) and As(V), respectively. The removal efficiency for the uptake of As(III) and As(V) ions over Fe3O4/CS/PEI nanocomposite at optimum conditions was found to be 99.5 and 99.7%, respectively. The experimental results were fitted using Freundlich’s and Langmuir’s isotherms. The data were more fitted to Langmuir isotherm providing a suggestion of monolayer adsorption with maximum adsorption capacity equal to 77.61 and 86.50 mg/g for the removal of As(III) and As(V), respectively. Moreover, linear regression coefficient (R2) indicated that the adsorption of arsenic ions over the synthesized magnetic nanocomposite obeyed pseudo 2nd order suggesting the chemisorption process. The reusability of the nanosorbent for arsenic uptake using sodium hydroxide as eluent was also assessed up to five cycles. Interestingly, Fe3O4/CS/PEI nanocomposite can be considered as a promising adsorbent for As ions’ removal from water and should be tested for the removal of other pollutants

The Application of Nanomaterials for the Electrochemical Detection of Antibiotics: A Review

Antibiotics can accumulate through food metabolism in the human body which may have a significant effect on human safety and health. It is therefore highly beneficial to establish easy and sensitive approaches for rapid assessment of antibiotic amounts. In the development of next-generation biosensors, nanomaterials (NMs) with outstanding thermal, mechanical, optical, and electrical properties have been identified as one of the most hopeful materials for opening new gates. This study discusses the latest developments in the identification of antibiotics by nanomaterial-constructed biosensors. The construction of biosensors for electrochemical signal-transducing mechanisms has been utilized in various types of nanomaterials, including quantum dots (QDs), metal-organic frameworks (MOFs), magnetic nanoparticles (NPs), metal nanomaterials, and carbon nanomaterials. To provide an outline for future study directions, the existing problems and future opportunities in this area are also included. The current review, therefore, summarizes an in-depth assessment of the nanostructured electrochemical sensing method for residues of antibiotics in different systems

The Synthesis of Magnetic Nitrogen-Doped Graphene Oxide Nanocomposite for the Removal of Reactive Orange 12 Dye

Herein, we report the nanofabrication of magnetic calcium ferrite (CaFe2O4) with nitrogen-doped graphene oxide (N-GO) via facile ultrasonication method to produce CaFe2O4/N-GO nanocomposite for the potential removal of reactive orange 12 (RO12) dye from aqueous solution. The successful construction of the nanocomposite was confirmed using different characterization techniques including scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform-infrared spectroscopy (FT-IR), and X-ray diffraction (XRD). The magnetic properties were studied using vibrating sample magnetometer (VSM) indicating ferromagnetic behavior of the synthesized materials that facilitate their separation using an external magnetic field after adsorption treatment. The addition of N-GO to CaFe2O4 nanoparticles enhanced the BET surface area from 24 to 52.93 m2/g as resulted from the N2 adsorption-desorption isotherm. The adsorption of the synthesized nanomaterials is controlled by several parameters (initial concentration of dye, contact time, adsorbent dosage, and pH), and the RO12 dye removal on the surface of CaFe2O4 nanoparticles and CaFe2O4/N-GO nanocomposite was reached through the chemisorption process as indicated from the kinetic study. The adsorption isotherm study indicated that the adsorption process of RO12 dye was best described through the Langmuir isotherm approving the monolayer adsorption. According to the Langmuir model, the maximum adsorption capacity for RO12 was 250 and 333.33 mg/g for CaFe2O4 nanoparticles and CaFe2O4/N-GO nanocomposite, respectively. The adsorption capacity offered by CaFe2O4/N-GO nanocomposite was higher than reported in the literature for adsorbent materials. Additionally, the regeneration study indicated that CaFe2O4/N-GO nanocomposite is reusable and cost-effective adsorbent. Therefore, the nanofabricated CaFe2O4/N-GO hybrid material is a promising adsorbent for water treatment