Facile Synthesis of the Polyaniline@Waste Cellulosic Nanocomposite for the Efficient Decontamination of Copper(II) and Phenol from Wastewater.

The existence of heavy metals and organic pollutants in wastewater is a threat to the ecosystem and a challenge for researchers to remove using common technology. Herein, a facile one-step in situ oxidative polymerization synthesis method has been used to fabricate polyaniline@waste cellulosic nanocomposite adsornt, polyaniline-embedded waste tissue paper (PANI@WTP) to remove copper(II) and phenol from the aqueous solution. The structural and surface properties of the synthesized materials were examined by XRD, FTIR, TEM, and a zeta potential analyzer. The scavenging of the Cu(II) and phenol onto the prepared materials was investigated as a function of interaction time, pollutant concentration, and solution pH. Advanced kinetics and isotherms modeling is used to explore the Cu(II) ion and phenol adsorption mechanisms. The synthesized PANI@WTP adsorbent showed a high intake capacity for Cu(II) than phenol, with the maximum calculated adsorption capacity of 605.20 and 501.23 mg g-1, respectively. The Langmuir equilibrium isotherm model is well-fitted for Cu(II) and phenol adsorption onto the PANI@WTP. The superior scavenging capability of the PANI@WTP for Cu(II) and phenol could be explained based on the host-guest interaction forces and large active sites. Moreover, the efficiency of the PANI@WTP for Cu(II) and phenol scavenging was excellent even after the five cycles of regeneration.

A Recent Progress in the Leachate Pretreatment Methods Coupled with Anaerobic Digestion for Enhanced Biogas Production: Feasibility, Trends, and Techno-Economic Evaluation.

Landfill leachate (LFL) treatment is a severe challenge due to its highly viscous nature and various complex pollutants. Leachate comprises various toxic pollutants, including inorganic macro/nano components, xenobiotics, dissolved organic matter, heavy metals, and microorganisms responsible for severe environmental pollution. Various treatment procedures are available to achieve better effluent quality levels; however, most of these treatments are nondestructive, so pollutants are merely transported from one phase to another, resulting in secondary contamination. Anaerobic digestion is a promising bioconversion technology for treating leachate while producing renewable, cleaner energy. Because of its high toxicity and low biodegradability, biological approaches necessitate employing other techniques to complement and support the primary process. In this regard, pretreatment technologies have recently attracted researchers' interest in addressing leachate treatment concerns through anaerobic digestion. This review summarizes various LFL pretreatment methods, such as electrochemical, ultrasonic, alkaline, coagulation, nanofiltration, air stripping, adsorption, and photocatalysis, before the anaerobic digestion of leachate. The pretreatment could assist in converting biogas (carbon dioxide to methane) and residual volatile fatty acids to valuable chemicals and fuels and even straight to power generation. However, the selection of pretreatment is a vital step. The techno-economic analysis also suggested the high economic feasibility of integrated-anaerobic digestion. Therefore, with the incorporation of pretreatment and anaerobic digestion, the process could have high economic viability attributed to bioenergy production and cost savings through sustainable leachate management options.

Fabrication of Polyaniline/Graphene Oxide Nanosheet@ Tea Waste Granules Adsorbent for Groundwater Purification.

The reuse and separation of nanomaterials from an aquatic solution is always challenging and may cause nanotoxicity if not separated completely. Nanomaterial immobilization on the surface of a macro-size material could be an effective approach to developing an efficient composite for groundwater purification. Herein, polyaniline and graphene oxide nanosheet immobilized granular tea waste (PANI/GO@GTW) has been synthesized to remove the anionic and cationic contaminants from groundwater. The synthesized materials were characterized by SEM, XRD, XPS, and FTIR spectroscopies. The optimization of experimental conditions was tested for bromide (Br−) removal from synthetic water. The results revealed that Br− adsorption behavior onto the synthesized materials was as follows: PANI/GO < PANI/GTW < PANI < PANI/GO@GTW. The optimum removal of Br− ions was observed at pH 3 with 90 min of saturation time. Br− adsorption onto PANI/GO@GTW followed the pseudo-first-order kinetic and Langmuir isotherm model, and electrostatic interaction was involved in the adsorption process. The optimum adsorption of Br− onto PANI/GO@GTW was found to be 26.80 m/g. The application of PANI/GO@GTW on real groundwater treatment demonstrated the effective removal of anion pollutants such as F−, Cl−, Br−, NO3−, and PO43−. This study revealed that PANI/GO@GTW successfully reduced Br− concentrations in synthetic and real groundwater and can be used for large-scale applications.

Experimental and Theoretical Studies of Methyl Orange Uptake by Mn-Rich Synthetic Mica: Insights into Manganese Role in Adsorption and Selectivity.

Manganese-containing mica (Mn-mica) was synthesized at 200 °C/96 h using Mn-carbonate, Al-nitrate, silicic acid, and high KOH concentration under hydrothermal conditions. Mn-mica was characterized and tested as a new adsorbent for the removal of methyl orange (MO) dye from aqueous solutions. Compared to naturally occurring mica, the Mn-mica with manganese in the octahedral sheet resulted in enhanced MO uptake by four times at pH 3.0 and 25 °C. The pseudo-second order equation for kinetics and Freundlich equation for adsorption isotherm fitted well to the experimental data at all adsorption temperatures (i.e., 25, 40 and 55 °C). The decrease of Langmuir uptake capacity from 107.3 to 92.76 mg·g-1 within the temperature range of 25-55 °C suggested that MO adsorption is an exothermic process. The role of manganese in MO selectivity and the adsorption mechanism was analyzed via the physicochemical parameters of a multilayer adsorption model. The aggregated number of MO ions per Mn-mica active site ( n ) was superior to unity at all temperatures signifying a vertical geometry and a mechanism of multi-interactions. The active sites number (DM) of Mn-mica and the total removed MO layers (Nt) slightly changed with temperature. The decrease in the MO adsorption capacities (Qsat = n·DM·Nt) from 190.44 to 140.33 mg·g-1 in the temperature range of 25-55 °C was mainly controlled by the n parameter. The results of adsorption energies revealed that MO uptake was an exothermic (i.e., negative ΔE values) and a physisorption process (ΔE < 40 kJ mol -1). Accordingly, the adsorption of MO onto Mn-mica was governed by the number of active sites and the adsorption energy. This study offers insights into the manganese control of the interactions between MO ions and Mn-mica active sites.

Fabrication of Novel Al(OH)3/CuMnAl-Layered Double Hydroxide for Detoxification of Organic Contaminants from Aqueous Solution.

A novel lamellar Al(OH)3/CuMnAl-layered double hydroxide (LDH) nanocomposite was successfully synthesized via the hydrothermal method and tested as a highly efficient adsorbent for the removal of Congo red (CR) dye from aqueous solution. Structural, morphological, and spectroscopic characterization of the Al(OH)3/CuMnAl-LDH nanocomposite were studied by X-ray diffraction, transmission electron microscopy, scanning electron microscopy, Fourier transform infrared spectroscopy, photoluminescence (PL) analysis, and UV-visible spectroscopy analysis techniques. The CR dye adsorption performance of the prepared materials increased with an increase in functionality. The adsorption capacity of the Al(OH)3/CuMnAl-LDH nanocomposite (172 mg/g, pH 7, temp 30 °C) was found to be higher than that of pure Al(OH)3 (32 mg/g, pH 7, temp 30 °C) and CuMnAl-LDH (102 mg/g, pH 7, temp 30 °C). The results revealed that anion exchange and hydrogen bonding are mainly responsible for the adsorption of CR onto the Al(OH)3/CuMnAl-LDH nanocomposite. Moreover, the adsorption of CR in the presence of Cu(II) and NaCl salt showed a synergistic and antagonistic effect while the presence of anionic Cr(VI) ions had no significant effect. The adsorption thermodynamics, isotherm, and kinetics modeling analyses were also conducted to study the interactions between CR molecules and the Al(OH)3/CuMnAl-LDH nanocomposite. The adsorption of CR was found to be endothermic and followed by the pseudo-second-order kinetics and the Langmuir adsorption isotherm model. The developed nanocomposite showed excellent potential for treating industrial wastewater.

Adsorptive removal of antibiotics from water over natural and modified adsorbents.

Various adsorbents including agricultural waste-based adsorbents, nanomaterials and layered double hydroxides have been reviewed for removal of antibiotics from water due to their unique properties. The adsorption mechanism is governed mostly by the affinity of a pollutant to adsorbent materials. However, the main adsorption mechanisms defined in this study for removal of antibiotics are the electrostatic attraction, π-π interaction and hydrogen bonding. The study highlighted the contribution of modification in the adsorption capacity of antibiotics. Some of the most important adsorbents discussed in this review are graphene-based adsorbents, binary layered double hydroxides and magnetic nanoparticles as well as the antibiotics sulfamethoxazole, tetracycline and metronidazole. The key factors for the selection of the suitable materials are the structure, characteristics and other physicochemical parameters such as pH and temperature. However, the most crucial factor is the adsorption capacity. Some of the adsorption kinetics models and isotherms for antibiotic sorption are also highlighted in this study. In addition, the review summarizes the future prospects and recent challenges faced with the adsorption techniques for removal of antibiotics from wastewater. This review will help readers understand the current trend in the adsorptive removal of antibiotics from water.

Iron chelation by polyamidoamine dendrimers: a second-order kinetic model for metal-amine complexation.

This study presents a kinetic model of the chelation of iron ions by generation 4 hydroxyl-terminated polyamidoamine (PAMAM) with ethylenediamine core (G4-OH). The coordination processes of iron ions from ferric chloride, FeCl(3), and ferrous bromide, FeBr(2), to G4-OH dendrimers were analyzed using ultraviolet-visible (UV-vis) spectroscopy, proton nuclear magnetic resonance ((1)H NMR) spectroscopy, and liquid chromatography-mass spectrometry (LC-MS). In the visible region, a charge-transfer was observed when the dendrimer was added to a ferric chloride solution. This phenomenon is a ligand-to-metal charge-transfer (LMCT) between the free electron group of the dendrimer's internal amines and the dehalogenated iron ion that takes 2 h to complete at room temperature. Analysis of potential rate laws and diffusion effects led to a second-order kinetic model for this reaction. By measuring the rate coefficients as a function of temperature (22-37 °C), an apparent activation energy of 41.5 kJ/mol was obtained using the Arrhenius method. The results of this study will fuel research of PAMAM dendrimers for environmental, pharmaceutical, and materials applications.