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In this study, the removal of a series of acid dyes by hybrid polymer adsorbent was investigated. Textile industry wastewater is mainly consisted of suspended solid particles and organic compounds with complex and nondecomposable structures. Treatment of such wastewaters has received much attention by researchers because of high water consumption and the presence of various chemical compounds, especially dyes. The use of polymers has recently attracted much attention for the treatment of textile wastewaters. According to the literature, hybrid polymers are highly capable of adsorbing dyes. In this research work, polyacrylamide/iron sulfate (PAM-FeSO₄) hybrid polymer was successfully synthesized through solution polymerization of acrylamide with ammonium persulfate and sodium thiosulfate and gradual addition of iron sulfate. The hybrid polymeric adsorbent was then used for removing acidic dyes with different chemical structures.

The effects of various experimental conditions and parameters, such as initial concentrations of dye and adsorbent, on the adsorption capacity of the adsorbent were investigated. The dye concentration was measured by an UV–vis spectrophotometer. The adsorption equilibrium was studied by plotting adsorption isotherms. The experimental data was fitted to Langmuir and Freundlich isotherms.

The adsorption experiments indicated that the PAM-FeSO₄ hybrid polymer has a high adsorption capacity (117.64 mg g⁻¹ for the Orange ІІ and 80.64 mg g⁻¹ for the Sunset Yellow [SY]) when 80 mg of adsorbent was immersed in the dye solution (1 g L⁻¹) with a pH of 11 at 25°C. The analysis of the equilibrium isotherms using the Langmuir and Freundlich isotherms indicated that the Langmuir model fit well to the experimental data.

To the best of the authors’ knowledge, this study is original. The removal of acid dyes such as Sunset Yellow and Methyl Orange using PAM-FeSO₄ hybrid polymer as flocculant was done for the first time.

Methylene blue (MB) is classified as a cationic dye which is widely used as chemical indicator, coloring agent and biological stain. The discharge of this dye to the water streams is harmful to the human beings. For this reason, this study investigated the removal of MB from aqueous solution by hydrogel nanocomposite.

In experimental part, at first, ultraviolet (UV)-curable hydrogel/chitosan nanocomposite, which improves its elasticity by urethane acrylate, was synthesized and characterized by FTIR and SEM analysis. Afterward, the synthesized hydrogel nanocomposite was applied for the removal of MB and the influence of operational condition including nanocomposite loading, dye concentration, contact time and pH of solution was specified. Moreover, isotherm studies as well as kinetics survey were performed.

Langmuir, Freundlich, Brunauer, Emmett and Teller and Tempkin adsorption isotherms were assessed for the analysis of experimental data indicating the Freundlich isotherm was the best fitted one. The adsorption kinetics data was examined indicating the adsorption kinetics appropriate to pseudo-second-order kinetics model.

The predominant water absorption property of the UV-curable hydrogel/chitosan nanocomposite to 8.5 steps and outstanding adsorption capacity for the elimination of MB on hydrogel nanocomposite subscribed that the synthesized hydrogel could be a favorable adsorbent for simultaneous absorption of water and removal of cationic dyes.

The disposal of wastewater containing silver is an environmental concern. Due to the toxicity of silver, treatment of such wastewater is necessary. Real wastewater contains a complex matrix of pollutants. The purpose of this paper is to study the adsorption behavior of silver in single and binary systems (with nickel) onto granular activated carbon.

The effect of silver ions concentration and the mass of adsorbent on the adsorption behavior were analyzed. Five two-parameter isotherms (Langmuir, Elovich, Freundlich, Dubinin–Radushkevich and Temkin) were applied to investigate the adsorption mechanism. Both linear and nonlinear regressions were tested for the first three isotherms. The experimental data were also fitted to Redlich–Petersons, Sips and Toth models.

A direct relationship between the initial silver ion concentration and its adsorption capacity was observed, whereas an inverse relationship between the adsorbent mass and the adsorption capacity was documented. The Langmuir model was found to best-fit the data indicating monolayer adsorption behavior. The maximum uptake was 2,500 mg/g in the single adsorption system. This value decreased to 909 mg/g in the binary system. The adsorption was found to have an exothermic chemical nature.

The study of the silver adsorption in a single system is inaccurate. Real wastewater contains a complex matrix of pollutants. This research gives a clear insight into the adsorption behavior in binary systems.

The purpose of this study was to the synthesis of Fe₃O₄@SiO₂ nanocomposites and using it as an adsorbent for removal of diazinon from aqueous solutions. Structural characteristics of the synthesized magnetic nanocomposite were described by Fourier transform infrared spectroscopy and scanning electron microscopy.

The effects of different parameters including pH (2-10), contact time (1-180 min), adsorbent dosage (100-2000 mg L⁻¹) and initial diazinon concentration (0.5–20 mg L⁻¹) on the removal processes were studied. Finally, isotherm and kinetic and of adsorption process of diazinon onto Fe₃O₄@SiO₂ nanocomposites were investigated.

The maximum removal efficiency of diazinon (96%) was found at 180 min with 1000 mg L⁻¹ adsorbent dosage using 0.5 mg L⁻¹ diazinon concentration at pH = 7. The experimental results revealed that data were best fit with the pseudo-second-order kinetic model (R² = 0.971) and the adsorption capacity was 10.90 mg g⁻¹. The adsorption isotherm was accordant to Langmuir isotherm.

In the present study, the magnetic nanocomposites were synthesized and used as an absorbent for the removal of diazinon. The developed method had advantages such as the good ability of Fe₃O₄@SiO₂ nanocomposites to remove diazinon from aqueous solution and the magnetic separation of this absorbent that make it recoverable nanocomposite. The other advantages of these nanocomposites are rapidity, simplicity and relatively low cost.

To treat water pollution, especially the contamination resulted from organic dyes has aroused significant attention around the world, this study aims to prepare the metal organic framework (MOF) materials hybridizing with poly(p-phenylene terephthalamide) (PPTA) by means of a facile refluxing method and to systematically investigate adsorption performance for anionic dye Congo red as target molecule from aqueous solution.

The MOF materials hybridized by PPTA were fabricated by virtue of a facile refluxing method, characterized by thermogravimetric analysis, X-ray powder diffraction, Fourier transform infrared and pore structure.

The results showed that pseudo-second-order kinetic model could better describe the adsorption process for all the four materials, whereas Elovich model also fitted the process for the hybrid materials with PPTA. Adsorption isotherm analyses indicated that Langmuir isotherm could be used to describe the adsorption process. Introduction of appropriate amount of PPTA could enhance the adsorption affinity of the MOF materials for Congo red, and the maximum adsorption capacity could reach as high as 1,053.41 mg/g while that of the MOF material without PPTA was 666.67 mg/g, indicating introduction of PPTA could change the microenvironment of the MOF materials and increase the adsorption sites, leading to high adsorption efficiency.

The microstructure of MOF hybridized materials in detail is the further and future investigation.

This study will provide a method to prepare MOF materials with high efficiency to treat anionic dyes like Congo red from aqueous solution.

Owing to the special characteristics of PPTA and similar to carbon tube, PPTA was introduced into MOF material to increased corresponding water stability. Because of aromatic ring and amide group on the surface of PPTA, the adsorption efficiency of the hybridized MOF material with appropriate amount of PPTA was greatly enhanced.

The purpose of this study is to focus on the preparation of macroporous adsorption resins (MARs) functionalized with carbazole and N-methylimidazole, and adsorption behaviors of (–)-epigallocatechin gallate (EGCG) and caffeine (CAF) on the functionalized MARs.

Based on the Friedel–Crafts and amination reactions, novel MARs functionalized with carbazole and N-methylimidazole were synthesized and characterized by the BET method. Accordingly, adsorption behaviors and structure-activity relationships for EGCG and CAF were studied in detail.

The results showed that pseudosecond-order kinetic model was provided with a better correlation for the adsorption of EGCG and CAF onto L-1 and L-2, and pseudofirst-order kinetic model was the most suitable model to illustrate the adsorption process for EGCG and CAF on L-3. The result indicated that Langmuir, Freundlich, Temkin–Pyzhev and Dubinin–Radushkevich isotherms all could better illustrate the adsorption processes of EGCG and CAF on L-1, L-2 and L-3.

This study provides theoretical guidance and technical support for the efficient separation and purification of EGCG and CAF from waste tea leaves by MARs on a large scale. In addition, the results showed that this novel MARs would provide useful help and be used in large-scale production of active ingredients from natural products in the industry and other fields.

Adsorption kinetic models such as pseudofirst-order, pseudosecond-order and intra-particle diffusion kinetic models, and adsorption isotherm models such as Langmuir, Freundlich, Temkin–Pyzhev and Dubinin–Radushkevich isotherms models were adopted to illustrate the adsorption mechanisms of EGCG and CAF. The main driving forces for MARs with no functional groups were pore sieving effects, p–p conjugation effects and hydrophobic interactions, and the other significant driving forces for MARs functionalized with carbazole and N-methylimidazole were electrostatic interactions, ion-dipole and hydrogen bonding interactions. This study might provide scientific references and useful help for large-scale separating and enriching active ingredients in natural products using the technology of MARs with special functional groups.

The purpose of this paper is to harness the potential of microwave pre-treatment to prepare carbon from locally available Sterculia foetida fruit shells for adsorption of heavy metals, particularly Nickel ions (Ni++), from effluent.

The pre-treatment methods comprise conventional methods as sun drying and oven drying as well as high intensity microwave drying. Response surface methodology was employed to analyse the optimization of the process. The adsorption behavioural characteristics of the material were established applying adsorption isotherms.

Adsorption of Ni++ was found to be effective in microwave drying at output power of 300 W. It was observed that the maximum adsorption capacity was attained at pH 6; an adsorbent dosage of 0.25 mgml−1 and initial metal ion concentration of 20 ppm with an interactive effect of initial concentration and dosage.

The research puts emphasise on prospecting of novel biomass for carbonization and application of the same for effective adsorption. Available literature on Sterculia foetida is very limited and this work will serve to create database on the amenability of processing.

Water is a vital natural resource without which life on earth would be impossible. Properties of synthetic dyes like high stability and noxious nature make it difficult to remove them from the effluent. This review focuses on the removal of synthetic dyes using nanoparticles (NPs) based on the adsorption principle.

Adsorption technique is widely used to remove synthetic dyes from their aqueous solution for decades. Synthetic dye removal using NPs is promising, less energy-intensive and has become popular in recent years. NPs are in high demand for treating wastewater using the adsorption principle due to their tiny size and vast surface area. To maximise environmental sustainability, the utilisation of green-produced NPs as efficient catalysts for dye removal has sparked attention amongst scientists.

This review has prioritised research and development of optimal dye removal systems that can be used to efficiently remove a large quantity of dye in a short period while safeguarding the environment and producing fewer harmful by-products. The removal efficiency of synthetic dye using different NPs in wastewater treatment varies mostly between 75% to almost 100%. This review will aid in the scaling up of the wastewater treatment process.

There is a lack of research emphasis on the safe disposal of NPs once the reuse efficiency significantly drops. The relevance of cost analysis is equally critical, yet only a few papers discuss cost-related information.

Comprehensive and planned research in this area can aid in the development of long-term wastewater treatment technology to meet the growing need for safe and reliable water emphasising reuse and desorption efficiency of the NPs.

In order to discover a new adsorbent that can be used to purify dye wastewater in the textile and apparel industry, a novel type of graphene oxide/gluten composite material using an improved acid bath coagulation method was synthesized, which can remove methylene blue in an aqueous environment.

After experimentally compounding different ratios of graphene oxide and gluten, the graphene oxide/gluten composite material with 20% graphene oxide content and superlative adsorption effect was chosen. The synthesized material was characterized by different techniques such as FT-IR and SEM, indicating the microstructure of the material and the success of the composite. Various factors were considered, namely, the influence of temperature, dosage, pH and contact time. The isotherms, kinetics and thermodynamic parameters were successively discussed.

The qmax value of 214.29 mg/g of the material was higher compared to the general sorbent, thus, the graphene oxide/gluten composite material was a suitable sorbent for methylene blue removal. Overall, the graphene oxide/gluten composite material can be considered as an effectual and prospective adsorbent to remove methylene blue in the textile and apparel industrial effluent.

Graphene oxide is a potentially excellent sorbent. However, the high dispersibility of GO is detrimental to adsorption, it disperses rapidly in an aqueous solution making separation and recovery difficult. The high load capacity and recyclability of gluten as a colloid make it a suitable carrier for fixing GO. Studies on the combination of GO and GT into composite adsorption material and for the removal of dyes from dyeing wastewater have not been reported. The composite material research on GO and GT can provide new ideas for the research of these kinds of materials and contribute to its wider and convenient application in wastewater treatment.

The purpose of this paper is to focus on the removal of hexavalent chromium [Cr(VI)] from wastewater by using activated carbon-supported Fe catalysts derived from walnut shell prepared using a wetness impregnation process. The different conditions of preparation such as impregnation rate and calcination conditions (temperature and time) were optimized to determine their effects on the catalyst’s characteristics.

The catalyst samples were characterized using thermogravimetric analysis, scanning electron microscopy and Fourier transform infrared spectroscopy. The adsorption of Cr(VI) by using using activated carbon supported Fe catalysts derived from walnut shell as an adsorbent and catalyst was investigated under different adsorption conditions. The parameters studied were contact time, adsorbent dose, solution pH and initial concentrations.

Results showed that higher adsorption capacity and rapid kinetics were obtained when the activated walnut shell was impregnated with Fe at 5 per cent and calcined under N₂ flow at 400°C for 2 h. The adsorption isotherms data were analyzed with Langmuir and Freundlich models. The better fit is obtained with the Langmuir model with a maximum adsorption capacity of 29.67 mg/g for Cr(VI) on Fe5-AWS at pH 2.0.

A comparison of two kinetic models shows that the adsorption isotherms system is better described by the pseudo-first-order kinetic model.