Development of cobalt-doped alumina hybrids for adsorption of textile effluents

The discharge volume and composition of textile effluents gain scientific concern due to hazardous and biotoxic nature of azo dyes. Azo dyes are non-biodegradable due to its complex molecular structure and recalcitrant nature. Serious attempts have been made to synthesize and develop new materials to combat the environmental problems. The present study is designed for removal of azo dyes (Methyl orange, Congo red and Basic fuchsine) from synthetic aqueous solutions and real textile effluents. For this purpose, cobalt-doped alumina hybrids are synthesized and applied as adsorbents in batch experiment. Two different aluminium precursor (aluminium nitrate and spent aluminium foil) and glucose are mixed following sol–gel method to get hybrids. The synthesized hybrids are characterized for surface and bulk properties using Fourier transform infrared, scanning electron microscopy and energy dispersive X-ray techniques. The characterization of materials under Fourier transform infrared revealed that –OH (3487–3504 cm −1 ), C–H (2935–2985 cm −1 ), Al–O–C (∼1380 cm −1 ), Al–O (∼ 800 cm −1 ), Al–O–Al (659–669 cm −1 ) and Co–O (583–589 cm −1 ) groups participate in the binding of dyes onto the surface of hybrids. Amorphous shaped particles and elemental composition (carbon, aluminium and oxygen) are demonstrated in scanning electron microscopy–energy dispersive X-ray micrograph. Time-dependent batch experiments under identical experimental parameters showed 74% of basic fuchsine, 68% of methyl orange and 85% maximum removal of Congo red onto the surface of cobalt-doped alumina hybrids probably through ion exchange mechanism. The experimental data when treated with adsorption models and isotherms, pseudo-second-order kinetic and Freundlich isotherm are found to be best fitted. The present study accomplishes the successful synthesis of novel and efficient cobalt-doped alumina hybrids provides environmental friendly and economical alternative option to the commercial adsorbents for the treatment of textile effluents

Hybrid mesoporous silicates: a distinct aspect to synthesis and application for decontamination of phenols

Water pollution due to organic compounds is of great concern and efforts are being made to develop efficient adsorbents for remediation of toxic pollutants. The development of new functionalized materials with increased performance is growing to meet the regulatory standards in response to public concerns for environment. In this study, an attempt has been made to investigate the influence of synthesis parameters like the reaction temperature, the surfactant-to-silica ratio and reaction time on the structural and textural properties of novel ordered mesoporous silica hybrids. In order to understand the effect of different synthesis parameters, all the prepared materials were systematically characterized by various analytical, spectroscopic and imaging techniques such as XRD, BET, TG etc. It was deduced from these studies that the synthesis temperature influence greatly the structural order whereas both the P104/Na2SiO3 molar ratio and reaction time found to influence textural properties significantly. However, under optimized experimental condition, we could achieve the functionalized silica hybrids that offers successful incorporation of -Amino, -Glucidoxy, -Methacrylate, -Vinyl and -Phenyl moieties indicated by FTIR peaks at 793 cm−1, 2870 cm−1, 796 cm−1, 1630 cm−1 and 954 cm−1. XRD studies reveal orthorhombic and tetragonal symmetry for the hybrids and these materials were found to be thermally stable due to incorporation of organic moiety in silica matrix. Functionalized silica hybrids then applied as adsorbents demonstrated efficient and comparable removal of 4-aminophenol and p-nitrophenol in 20 min facilitated through organic moiety. Detailed modeling of the sorption using equilibrium and kinetic isotherms has been carried out to get an insight into the transport process. The adsorption isotherms of phenol derivatives are well-fitted with the Langmuir, Freundlich and Temkin Isotherms and the adsorption kinetics follows the pseudo second order model. The modeling confirms that the uptake is a chemisorption process

On the Behavior of Newly Synthesized Functionalized Imidazolium-Based Ionic Liquids for Highly Efficient Extraction and Separation of Pirimicarb from Orchard Real Wastewater

The presence of pirimicarb compounds as pollutants in orchard wastewater has sparked rising worries about their detrimental impacts on the ecosystem and human health, and their removal is critical for Pakistan’s aquatic environment. It not only contaminates fruit, but it also leaches into the soil and contaminates groundwater. However, there is little data on the effective removal of pirimicarb from orchard wastewater. The main purpose of this study is to create a novel family of functionalized imidazolium-based ionic liquids (ILs) using a simple chemical process, which will be utilized for the first time to extract pirimicarb from orchard wastewater in an efficient, cost-effective, and environmentally acceptable manner. FTIR, SEM, XRD, TGA, BET, and 1H NMR spectroscopy were used to characterize the functionalized samples. The impact of the IL substituent on the separation capacity was studied. In addition, the extraction and separation of pirimicarb from orchard wastewater were investigated under a variety of conditions (time, concentration, and temperature) in order to better understand the adsorption behaviors of distinct ILs in an aqueous solution. The adsorption equilibrium was reached in 30 minutes, and the maximum removal of pirimicarb was achieved utilizing the synthesized [C2im][C3H6NH2]Br-, according to the data. The pseudo-first-order model and the Langmuir model both suit well with the adsorption mechanism of pirimicarb with very good adsorptive capacities. Thermodynamic analyses indicated spontaneous, endothermic, and entropy-driven adsorption processes. The synthesized imidazolium-based ILs have good regeneration capability and recycling at least for six adsorption-desorption runs and have also been used to successfully detect pirimicarb orchard wastewater samples. The superior safety of the proposed method nominates it as a promising future strategy for pollution prevention. Consequently, this work has proven that the pirimicarb adsorption to various imidazolium-based ILs was dependent on the structures of the produced imidazolium-based ILs, which specifies its potential for practical applications in water pollutant removal and environmental remediation

Chemodynamics of Methyl Parathion and Ethyl Parathion: Adsorption Models for Sustainable Agriculture

The toxicity of organophosphate insecticides for nontarget organism has been the subject of extensive research for sustainable agriculture. Pakistan has banned the use of methyl/ethyl parathions, but they are still illegally used. The present study is an attempt to estimate the residual concentration and to suggest remedial solution of adsorption by different types of soils collected and characterized for physicochemical parameters. Sorption of pesticides in soil or other porous media is an important process regulating pesticide transport and degradation. The percentage removal of methyl parathion and ethyl parathion was determined through UV-Visible spectrophotometer at 276 nm and 277 nm, respectively. The results indicate that agricultural soil as compared to barren soil is more efficient adsorbent for both insecticides, at optimum batch condition of pH 7. The equilibrium between adsorbate and adsorbent was attained in 12 hours. Methyl parathion is removed more efficiently (by seven orders of magnitude) than ethyl parathion. It may be attributed to more available binding sites and less steric hindrance of methyl parathion. Adsorption kinetics indicates that a good correlation exists between distribution coefficient (Kd) and soil organic carbon. A general increase in Kd is noted with increase in induced concentration due to the formation of bound or aged residue

Synthesis of a cobalt-based photoluminescent coordination complex to study quenching mechanisms of nitro compounds

<p>A cobalt metal coordination complex was synthesized using the bipyridyl spacer ligand along with a dicarboxylate as secondary ligand. The coordination complex was characterized using FTIR, ¹H NMR, elemental analysis, thermogravimetric analysis, and powder XRD. The structure shown from single-crystal XRD revealed that each Co(II) cation in the cluster can be described as trigonal bipyramidal. Luminescence properties of the complex were investigated using different solvents. The photoluminescence (PL) spectra depicted change in band gap for THF and DCM. The complex was further investigated for ligand-based photoluminescence properties and thus used for sensing of nitro compounds. The static and dynamic quenching mechanism of nitro compounds was identified through the Stern–Volmer model.</p

Synthesis, characterisation and photocatalytic performance of ZnS coupled Ag2S nanoparticles: A remediation model for environmental pollutants

The growing demand of industries has led to environmental degradation due to excessive release of toxic chemicals. Nanotechnology has developed to combat the impacts integrated with industrial revolution. The present investigation proposes a remediation model for toxic dyes and poly aromatic hydrocarbons by effective use of nanotechnology. For this purpose, zinc sulphide (ZnS), silver sulfide (Ag2S) and bimetallic ZnS-Ag2S are synthesized from a single source precursor and evaluated as potential photocatalytic agents. The synthesized nanoparticles were characterized by a range of techniques like UV–visible, PL, XRD, EDX, TEM and TGA. The results indicated that prepared nanoparticles were crystalline, spherical in shape, possess obvious atomic planes with a size in the range of 6–12 nm.Each of the synthesized material was tested as potential photocatalyst candidate for the degradation of representative azo-dyes (Crystal Violet, Congo Red) and polyaromatic hydrocarbons (Naphthalene, Phenanthrene and Pyrene) under visible light irradiation source. The degradation efficiency of the synthesized nanoparticles was calculated to be more than 70% for Crystal Violet and 80%for Congo Red upon contact with the dye solutions for 50 min and pseudo second order kinetic model was found to be the best fit. The synthesized nanoparticles were also effective in its own significance for the degradation of polyaromatic hydrocarbons. The fragmentation study of polyaromatic hydrocarbons using nanoparticles postulates that phthalic acid pathway is the predominant mechanism for PAHs. It is recommended that environmental compartment with mix pollutants can conveniently be treated with a single material to an appreciable extent. The study offers economical and environment friendly remediation model. Keywords: Single source precursor, Azo-dyes, Poly aromatic hydrocarbons, Environmental remediation, Photocatalysi

Remediation of deltamethrin contaminated cotton fields: residual and adsorption assessment

Pakistan occupies a significant global position in the growing of high quality cotton. The extensive application of pesticides on agricultural products leads to environmental risk due to toxic residues in air, water and soil. This study examined the chemodynamic effect of Deltamethrin on cotton fields. Samples were collected from the cotton fields of D.G. Khan, Pakistan and analyzed for heavy metal speciation patterns. Batch experiments were administered in order to study the adsorption of Deltamethrin in cotton fields. The effect of different factors including pH, adsorbate dose, and adsorbent mass on adsorption were studied. It was observed that in general, adsorption increased with increases in the mass of adsorbate, although the trends were irregular. Residual fractions of deltamethrin in the soil and water of cotton fields were analyzed to assess concentrations of xenobiotics bound to soil particles. Results indicated that such residues are significantly higher in soil samples due to high Koc in comparison to water, indicating the former is an efficient degradation agent. Results from the batch experiment resulted in 95% removal with alkaline pH and an adsorbent-adsorbate ratio of 250:1. These results may be used to environment friendly resource management policies

Development of Ag0.04ZrO2/rGO heterojunction, as an efficient visible light photocatalyst for degradation of methyl orange

Abstract Methyl orange (MO) is mutagenic, poisonous, and carcinogenic in nature, hence, effective methods are required for its degradation. We have synthesized pure ZrO2, Ag-doped ZrO2, and Ag-doped ZrO2/rGO as hybrid photocatalysts by facile hydrothermal method. These photocatalysts were characterized by powder XRD, scanning electron microscopy, EDX, FTIR, photoluminescence, UV–Vis diffuse reflectance (DRS), and Raman spectroscopy. The photodegradation of MO (10 ppm) was studied with pure ZrO2, Ag-doped ZrO2, and Ag-doped ZrO2/rGO (10 mg/100 mL catalyst dosage) photocatalysts at 100 min irradiation time under UV–Visible light. The pH effect and catalyst dosage on photodegradation of MO was investigated. Ag0.04ZrO2/rGO photocatalyst exhibited the maximum photocatalytic degradation of MO (87%) as compared to Ag0.04ZrO2 (60%) and pure ZrO2 (26%). Reusability experiments ensured the excellent stability of photocatalyst after five consecutive experiments. To the best of our knowledge, this is the first report on the facile hydrothermal synthesis of Ag0.04ZrO2/rGO photocatalyst for photocatalytic degradation of methyl orange