Biocomposite based on zirconium and amine-grafted walnut shell with antibacterial properties for the removal of Alizarin red in water: batch and column studies.

Recent progress has been made in the application of novel zirconium-loaded amine-grafted walnut shells as multifunctional adsorbents for the remediation of Alizarin red (AR) and bacteria in aqueous solutions. The morphology and functional groups of ACWNS@Zr were studied using Brunauer-Emmett-Teller (BET) techniques, X-ray diffraction (XRD), pH point of zero charges (pHpzc), scanning electron microscopy (SEM), and Fourier transform infrared (FTIR) spectroscopy. Adsorption and regeneration tests were carried out in batch and column mode. The ACWNS@Zr had a Langmuir maximum capacity of 415.5 ± 6.1 mg g-1 at 303 K. The spread plate technique was used to evaluate the adsorbent's antimicrobial properties against Staphylococcus aureus and Escherichia coli. ACWNS@Zr exhibited inhibitory potential towards S. aureus and E. coli in the suspensions by 53.3% and 15.0%, respectively. Electrostatic interaction and complexation interaction could be the key mechanisms governing AR dye removal. Equilibrium isotherms fit Langmuir models better for both batch and column studies, while adsorption kinetics to pseudo-second-order and Thomas models for batch and column studies, respectively. Thermodynamic studies indicated that the adsorption process was endothermic and spontaneous. Furthermore, columns' mass transfer capacity (B) increased as the concentration increased due to the enhanced driving force for AR adsorption onto ACWNS@Zr. Regeneration with NaOH solution of AR-loaded ACWNS@Zr was remarkable.

Efficient removal of 2,4-D from solution using a novel antibacterial adsorbent based on tiger nut residues: adsorption and antibacterial study.

We engineered a tiger nut residue (TNR, a low-cost agricultural waste material) through a facile and simple process to take advantage of the introduced functional groups (cetylpyridinium chloride, CPC) in the removal of 2,4-dichlorophenoxyacetic acid (2,4-D) in batch mode and further investigated its impingement on bacterial growth in a yeast-dextrose broth. The surface characterizations of the adsorbent were achieved through Fourier-transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller method (BET), X-ray diffraction analysis (XRD), and X-ray photoelectron spectroscopy (XPS). The batch adsorption studies revealed that solution pH, adsorbent dose, temperature, and salt affected the adsorptive capacity of TNR-CPC. The equilibrium data were best fitted by Langmuir isotherm model with a maximum monolayer adsorption capacity of 90.2 mg g-1 at 318 K and pH 3. Pseudo-second-order model best fitted the kinetics data for the adsorption process. Physisorption largely mediated the adsorption system with spontaneity and a shift in entropy of the aqueous solid-solute interface reflecting decreased randomness with an exothermic character. TNR-CPC demonstrated a good reusability potential making it highly economical and compares well with other adsorbents for decontamination of 2,4-D. The adsorption of 2,4-D proceeded through a probable trio-mechanism; electrostatic attraction between the carboxylate anion of 2,4-D and the pyridinium cation of TNR-CPC, hydrogen bonding between the hydroxyl (-OH) group inherent in the TNR and the carboxyl groups in 2,4-D and a triggered π-π stacking between the benzene structures in the adsorbate and the adsorbent. TNR-CPC reported about 99% inhibition rate against both gram-positive S. aureus and gram-negative E. coli. It would be appropriate to investigate the potential of TNR-CPC as a potential replacement to the metal oxides used in wastewater treatment for antibacterial capabilities, and its effects against airborne bacteria could also be of interest.

Adsorption performance of modified agricultural waste materials for removal of emerging micro-contaminant bisphenol A: A comprehensive review.

This review is an attempt to assess the adsorption performance of different green adsorbents derived from agricultural waste materials (AWMs) that were used for the elimination of bisphenol A (BPA) from aqueous matrices. Different processes including grafting, polymerization, activation and chemical treatment have been applied to functionalize and modify agricultural waste materials for the purposes of increasing their adsorptive performances toward BPA. The highest reported adsorption capacity of adsorbent from agricultural waste for the uptake of BPA is the highly microporous carbon adsorbent derived from Argan nut shell (1408 mg g-1). Hydrogen bonding, hydrophobic and π-π interactions were reported in most studies as the main mechanisms governing the adsorption of BPA onto agricultural waste adsorbents. Equilibrium isotherm and kinetic studies for the uptake of BPA onto agricultural waste adsorbents were best described by Langmuir/Freundlich model and pseudo-second order model, respectively. Despite the effective elimination of BPA by various agricultural waste adsorbents, an appropriate selection of elution solvent is important for effective desorption of BPA from spent adsorbent. To date, ethanol, diethyl ether-methanol, methanol-acetic acid, mineral acids and sodium hydroxide are the most eluents applied for desorption of BPA molecules loaded onto AW-adsorbents. Looking toward the future, studies on the agricultural waste adsorbents based on polymers, activated carbons, nanoparticles and highly microporous carbons should be mostly considered by the researchers toward removing BPA. These future studies should be performed both in laboratory, pilot and industrial scales, and also should report the sustainable techniques for disposal of the spent AW-adsorbents after lose their adsorption performance on BPA.

Decontamination of bisphenol A and Congo red dye from solution by using CTAB functionalised walnut shell.

In this research, the eco-friendly cationic surfactant modified walnut shell (WNS-CTAB) was synthesised to enhance the uptake for bisphenol A (BPA) and Congo red (CR) from aqueous solution. The characterisation of WNS-CTAB was performed using Fourier-transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), etc. to know its physiochemical properties. The adsorption equilibrium results were best described by the Langmuir isotherm model, which confirmed the monolayer adsorption of the pollutant molecules onto the adsorbent's surface. The maximum monolayer adsorption quantity of WNS-CTAB was established to be 38.5 mg g-1 for BPA and 104.4 mg g-1 for CR at 303 K, respectively. Pseudo-second-order kinetic models described the adsorption kinetics of both BPA and CR. Furthermore, the intra-particle diffusion was applied to analyse the kinetic results and was established that the rate was not solely controlled by diffusion. The mechanisms associated with BPA and CR adsorption onto the WNS-CTAB may include van der Waals interaction, hydrophobic interaction, and electrostatic force. WNS-CTAB demonstrated a good reusability potential with desorption through three successive adsorption-desorption cycles performed in both experiments. Moreover, in the binary system, the adsorption capacity of BPA witnessed a 66% decrease while CR saw marginal reduction of 8.0 %. This suggests that WNS-CTAB had a higher affinity for binding to CR with higher selectivity as compared with BPA. Therefore, WNS-CTAB has exhibited huge potential to serve as a functional material for practical use in the treatment of wastewater.

Fe3O4 and iminodiacetic acid modified peanut husk as a novel adsorbent for the uptake of Cu (II) and Pb (II) in aqueous solution: Characterization, equilibrium and kinetic study.

The presence of higher concentrations of heavy metals in water affects its quality with a concomitant adverse effect on its users thus their removal is paramount. A novel adsorbent, PN-Fe3O4-IDA derived from the chemical modification of peanut husk (a low-cost agricultural biomass produced in significant quantities globally) using magnetic nanoparticles (Fe3O4) and iminodiacetic acid was utilized for the remediation of heavy metals in aqueous solution. Analytical techniques vis-à-vis the Fourier-Transform Infrared, Scanning Electron Microscope, Brunauer-Emmett-Teller, X-ray photoelectron spectroscopy and X-ray Diffraction were applied for the characterization of PN-Fe3O4-IDA. Results from the characterization studies showed that PN-Fe3O4-IDA possessed a mesoporous structure, a heterogeneous surface and functional groups such as carboxylic acid and a tertiary nitrogen atom which enhanced its adsorption capacities as well as magnetic properties which ensured its easy removal from the solution using a magnet. The maximum uptake of Pb and Cu onto PN-Fe3O4-IDA was 0.36 and 0.75 mmol g-1 (at 318 K) respectively with the chemisorption process being the major reaction pathway for the processes. The synthesized adsorbent exhibits significant adsorption capacity for the selected pollutants as well as some unique features which promotes its use as an adsorbent for wastewater remediation processes.

Rational Design of Far-Red to Near-Infrared Emitting Carbon Dots for Ultrafast Lysosomal Polarity Imaging.

Carbon dots (CDs) have been widely studied for their excellent properties. However, most of the prepared CDs only show strong emission in the blue to green region, which greatly limits the application of CDs in the biomedical field. In this report, a new design strategy of long-wavelength CDs was reported. The orange phenyl-CDs with good optical properties and biocompatibility were successfully prepared by changing the substituted group of the o-phenylenediamine and the main emission band of phenyl-CDs was in the far-red region. With the increase of polarity, the wavelength of phenyl-CDs red-shifts and the fluorescence intensity decreases, demonstrating their sensitive polarity response function. In addition, phenyl-CDs can achieve ultrafast target imaging of lysosome within 40 s through clathrin-mediated endocytosis. Finally, phenyl-CDs were successfully applied for monitoring lysosomal polarity induced by drugs, which is helpful in getting a better understanding of the physiological and pathological processes of lysosomes. This report provides an important theoretical basis for the rational design and precise synthesis of long-wavelength fluorescent CDs.

Iminodiacetic acid functionalized magnetic peanut husk for the removal of methylene blue from solution: characterization and equilibrium studies.

A novel adsorbent PN-Fe3O4-IDA was developed by the chemical modification of magnetic peanut husk with iminodiacetic acid (IDA) and its efficacy for the sequestration of cationic dyes assessed using methylene blue (MB) as a model. This modification process enhanced the adsorption capacity of peanut husk as an adsorbent for dye sequestration and at the same time greatly minimized the adverse effects associated with its use in the pristine state. Results from the batch adsorption studies indicated that the uptake of MB onto PN-Fe3O4-IDA increased with MB concentration, contact time, temperature and pH whereas it decreased in the presence of some common salts. The pseudo-second-order kinetic model was observed to best describe the adsorption process which may greatly be influenced by the intra particle diffusion mass transfer. A maximum monolayer adsorption capacity of 43.5 mg g-1 was observed at 313 K according to the Langmuir model. There was good property of regeneration for MB-loaded PN-Fe3O4-IDA. Based on these results, as well as other unique features such as easy separation and preparation under benign environmental conditions, PN-Fe3O4-IDA exhibits great potential for the removal of MB and other cationic pollutants in practical applications with easy separation from solution using external magnet. Graphical abstract.

Uptake of micropollutant-bisphenol A, methylene blue and neutral red onto a novel bagasse-ß-cyclodextrin polymer by adsorption process.

The presence of emerging micropollutants and dyes in water resource has raised global concern about their intense effects to aquatic environments, ecosystem and human health in general. So far, various adsorbents have been suggested for reducing the levels of bisphenol A, methylene blue and neutral red contamination in wastewaters. However, a number of these adsorbents seemed to have low adsorptive capacities and regeneration performances. In view of these, batch experiment was performed to decontaminate these pollutants from aqueous solutions using an optimized bagasse-ß-cyclodextrin polymer (SB-ß-CD). Characterization studies of SB-ß-CD were performed using FTIR, pH point of zero charge, XRD and BET methods. Adsorption of BPA, MB and NR was favored at lower temperature (298 K) and pH of 7.0, 9.0 and 6.0, respectively. The maximum adsorption capacity of BPA, MB and NR at 298 K was 121, 963 and 685 mg g-1, respectively. Hydrogen bonding through host-guest inclusion and electrostatic interactions could respectively attribute to uptake of BPA and MB/NR onto SB-ß-CD. Adsorption kinetics of three pollutants followed pseudo-second-order model. Langmuir and Freundlich models were fitted to describe the adsorption of BPA and MB/NR, respectively. Thermodynamic parameters confirmed the occurrence of physical adsorption which is spontaneous and exothermic in nature. SB-ß-CD loaded with BPA and MB/NR was certainly reused by 75% ethanol and 0.1 mol L-1 HCl solutions, respectively. Novel SB-ß-CD showed better adsorptive capacity and regeneration performances; consequently can offers practical application for removal of BPA, MB and NR from wastewaters.