Advanced applications of hydroxyapatite nanocomposite materials for heavy metals and organic pollutants removal by adsorption and photocatalytic degradation: A review.

This comprehensive review delves into the forefront of scientific exploration, focusing on hydroxyapatite-based nanocomposites (HANCs) and their transformative role in the adsorption of heavy metals (HMs) and organic pollutants (OPs). Nanoscale properties, including high surface area and porous structure, contribute to the enhanced adsorption capabilities of HANCs. The nanocomposites' reactive sites facilitate efficient contaminant interactions, resulting in improved kinetics and capacities. HANCs exhibit selective adsorption properties, showcasing the ability to discriminate between different contaminants. The eco-friendly synthesis methods and potential for recyclability position the HANCs as environmentally friendly solutions for adsorption processes. The review acknowledges the dynamic nature of the field, which is characterized by continuous innovation and a robust focus on ongoing research endeavors. The paper highlights the HANCs' selective adsorption capabilities of various HMs and OPs through various interactions, including hydrogen and electrostatic bonding. These materials are also used for aquatic pollutants' photocatalytic degradation, where reactive hydroxyl radicals are generated to oxidize organic pollutants quickly. Future perspectives explore novel compositions, fabrication methods, and applications, driving the evolution of HANCs for improved adsorption performance. This review provides a comprehensive synthesis of the state-of-the-art HANCs, offering insights into their diverse applications, sustainability aspects, and pivotal role in advancing adsorption technologies for HMs and OPs.

Advances and future perspectives of water defluoridation by adsorption technology: A review.

Fluoride contamination in water sources poses a significant challenge to human health and the environment. In recent years, adsorption technology has emerged as a promising approach for water defluoridation due to its efficiency and cost-effectiveness. This review article comprehensively explores the advances in water defluoridation through adsorption processes. Various adsorbents, including natural and synthetic materials, have been investigated for their efficacy in removing fluoride ions from water. The mechanisms underlying adsorption interactions are elucidated, shedding light on the factors influencing defluoridation efficiency. Moreover, the review outlines the current state of technology, highlighting successful case studies and field applications. Future perspectives in the field of water defluoridation by adsorption are discussed, emphasizing the need for sustainable and scalable solutions. The integration of novel materials, process optimization, and the development of hybrid technologies are proposed as pathways to address existing challenges and enhance the overall efficacy of water defluoridation. This comprehensive assessment of the advances and future directions in adsorption-based water defluoridation provides valuable insights for researchers, policymakers, and practitioners working towards ensuring safe and accessible drinking water for all.

Removal of food dyes using biological materials via adsorption: A review.

It is alarming that synthetic food dyes (FD) are widely used in various industries and that these facilities discharge their wastewater into the environment without treating it. FDs mixed into industrial wastewater pose a threat to the environment and human health. Therefore, removing FDs from wastewater is very important. This review explores the burgeoning field of FD removal from wastewater through adsorption using biological materials (BMs). By synthesizing a wealth of research findings, this comprehensive review elucidates the diverse array of BMs employed, ranging from algae and fungi to agricultural residues and microbial biomass. Furthermore, this review investigates challenges in practical applications, such as process optimization and scalability, offering insights into bridging the gap between laboratory successes and real-world implementations. Harnessing the remarkable adsorptive potential of BMs, this review presents a roadmap toward transformative solutions for FD removal, promising cleaner and safer production practices in the food and beverage industry.

Effective removal of Allura red food dye from water using cross-linked chitosan-diatomite composite beads.

Chitosan (Ch)-diatomite (D) composite beads (Ch-D) were synthesized using epichlorohydrin and tripolyphosphate crosslinkers and then moulded into uniform beads in tripolyphosphate solution. FT-IR and SEM-EDX analyses showed that Ch-D composite adsorbent was successfully synthesized by functionalization of chitosan to Ch-D by hydrogen bonding and electrostatic interactions and improved adsorption capacity for removal of Allura red AC (AR) food dye. The removal rate of AR food dye was found to be 98 % at 25 °C, natural AR dye pH value, 24 h, and at the initial AR dye concentration of 200 mg L-1. The maximum adsorption capacity was found to be 34.7 mg g-1. It was observed that π-π interactions, hydrogen bonds, and electrostatic interactions between the functional groups containing oxygen and amine on the surface of the Ch-D composite and the functional groups of the anionic AR dye, and AR dye adsorption via complexation took place. In light of all this information, the Ch-D composite adsorbent is a promising potential material for the effective treatment of colored pollutants from wastewater.

High-Performance Material for the Effective Removal of Uranyl Ion from Solution: Computationally Supported Experimental Studies.

Adsorption is a widely used method for pollution removal and for the recovery of valuable species. In recent years, the use of metal-organic compounds among the adsorbents used in adsorption studies has increased. In this study, the performance of the water-insoluble Fe complex as a metal organic framework (MOF-Fe-Ta) of water-soluble tannic acid, which is not used as an adsorbent in uranium recovery and removal, was investigated. For the characterization of the new synthesized material, Fourier transform infrared, scanning electron microscopy, and X-ray diffraction analyses were performed. The changes in the adsorption process based on various parameters were investigated and discussed. The point of zero charges value of the adsorbent was found as 5.52. It was noticed that the adsorption increases as the pH increases. Analyzing the effect of concentration on adsorption, we determined which model explained the adsorption better. The monolayer capacity of the adsorbent determined in light of the Langmuir model was reported as 0.347 mol kg-1. The Freundlich constant, namely the ß value obtained in the Freundlich model, which is a measure of surface heterogeneity, was found to be 0.434, and the EDR value, which was found from the Dubinin-Raduskevich model and accepted as a measure of adsorption energy, was 10.3 kJ mol-1. The adsorption was kinetically explained by the pseudo-second-order model and the adsorption rate constant was reported as 0.15 mol-1 kg min-1. The effect of temperature on adsorption was studied; it was emphasized that adsorption was energy consuming, that is, endothermic and ΔH was found as 7.56 kJ mol-1. The entropy of adsorption was positive as 69.3 J mol-1 K-1. As expected, the Gibbs energy of adsorption was negative (-13.1 kJ mol-1 at 25 °C), so adsorption was considered as a spontaneous process. Additionally, the power and mechanism of the interaction between studied adsorbent and adsorbate are explained through density functional theory computations. Computationally obtained data supported the experimental studies.

Synthesis and characterization of chitosan-vermiculite-lignin ternary composite as an adsorbent for effective removal of uranyl ions from aqueous solution: Experimental and theoretical analyses.

Chitosan (Ch), vermiculite (V) and lignin (L) were used as the components of a natural composite adsorbent (Ch-VL) for the removal of the UO22+ ions in aqueous solutions. During the study, we recorded and analyzed the initial UO22+ ion concentration, initial pH, contact time, temperature, and recovery. The recycling performance of the Ch-VL composite was assessed by three sequential adsorption/desorption experiments. Adsorption performance of the Ch-VL composite for UO22+ ions was 600 mg L-1 at pH 4.5 and temperature of 25 °C. Thermodynamic findings, ΔH0:28.1 kJ mol-1, and ΔG0:-14.1 kJ mol-1 showed that adsorption behavior was endothermic and spontaneous. Its maximum adsorption capacity was 0.322 mol kg-1, obtained from the Langmuir isotherm model. The adsorption kinetics indicated that it followed the pseudo-second-order and intraparticle diffusion rate kinetics. The adsorption thermodynamic shown indicated that the UO22+ ion adsorption was both spontaneous and endothermic. The adsorption process was enlightened by FT-IR and SEM-EDX analyses. The study suggested a simple and cost-effective approach for the removal of toxic UO22+ ions from wastewater. To highlight the adsorption mechanism, DFT calculations were performed. Theoretical results are in good agreement with experimental observations.

Treatment of the Allura Red food colorant contaminated water by a novel cyanobacterium Desertifilum tharense.

The biosorption properties of a newly isolated and identified cyanobacterium called Desertifilum tharense were investigated in the current study. Following morphological and molecular identification (16S rRNA sequencing analysis), the food colorant removal potential of this new isolate was determined. Moreover, the isotherm, kinetic, and thermodynamic studies were performed, and also the biosorbent characterization was studied after and before colorant biosorption with Fourier transform infrared and scanning electron microscopy analysis. Additionally, the changes in chlorophyll content of the biosorbent were examined after and before colorant treatment. The newly isolated cyanobacterial biosorbent removed 97% of Allura Red food colorant/dye at 1,500 mg L-1 initial dye concentration successfully at optimal conditions. Langmuir isotherm and pseudo-second-order kinetic models were fitted with the biosorption of the dye. The D-R model showed that the biosorption process occurred physically. The chlorophyll-a content of the biosorbent was negatively affected by the biosorption. The newly isolated and identified cyanobacterium seems to be a successful candidate for use to treat highly dye concentrated wastewaters.

Epichlorohydrin and tripolyphosphate-crosslinked chitosan-kaolin composite for Auramine O dye removal from aqueous solutions: Experimental study and DFT calculations.

Chitosan (Ch, a natural polymer) and kaolin (K, a natural mineral) composite (Ch-K) was produced with the help of two crosslinkers, epichlorohydrin and tripolyphosphate, and then moulded into uniform beads in tripolyphosphate solution. The synthesis was proved by the analyses involving FT-IR and SEM-EDX. The beads were then used as the natural adsorbent for removal of the auramine O (AO), a frequently-used industrial dye, in aqueous solutions. Adsorbent performance of the Ch-K composite for AO dye molecules was optimized: 500 mg L-1 at pH 7.5 at 25 °C. The Langmuir model found 0.118 mol kg-1 for the maximum adsorption capacity of the Ch-K and the D-R isotherm model showed that the nature of the adsorption process was physical. Kinetics of the adsorption could be explained by using both IPD (intraparticle diffusion) and PSO (pseudo second order) models. Thermodynamic parameters demonstrated that the behaviour of the adsorption was an endothermic and spontaneous. The activity of the composite adsorbent was recovered (88%) after the five sequential adsorption/desorption cycles. Supported by experimental findings, the results obtained from in silico modeling at M06-2X/6-31+G (d,p) level helped hypothesise a mechanism for the formation of the Ch-K composite, and shed some light onto the adsorption behaviour of AO dye by assuming several favourable intermolecular interactions.

A chitosan-based composite for adsorption of uranyl ions; mechanism, isothems, kinetics and thermodynamics.

The present paper describes a green and cost-effective approach to investigate chitosan-sepiolite (Ch-Sep) composite as an adsorbent for removal of UO22+ ions in aqueous solution. The Ch-Sep composite was prepared as a beads using with two cross-linking agents: tripolyphosphate (TPP) and epichlorohydrin (ECH). Their adsorption properties for the removal of UO22+ ions in aqueous solution by batch experimental conditions were studied. The adsorptive removal processes of UO22+ ions from aqueous solution were evaluated by Langmuir, Freundlich and Dubinin-Radushkevich isotherm models, and was found to be perfectly fit to the Langmuir model (R2 = 0.971). The maximum adsorption capacity was 0.220 mol kg-1 at 25 °C from Langmuir isotherm model. Adsorption energy was 12.1 kJ mol-1 indicating that the adsorption process was chemical. The adsorption kinetics followed the pseudo second order and intra particle diffusion models. The thermodynamics parameters of UO22+ ions removal from aqueous solution was confirmed spontaneous, endothermic and possible at higher temperatures behavior of adsorption process. The adsorption mechanism of UO22+ ions onto Ch-Sep composite beads was investigated by FT-IR and SEM analysis. These findings revealed the effectiveness and potential of the newly synthesized Ch-Sep composite beads for the removal of UO22+ ions.

Bio-sorption of bisphenol a by the dried- and inactivated-lichen (Pseudoevernia furfuracea) biomass from aqueous solutions.

Bisphenol A (BPA), which is known as one of the endocrine-disrupting chemicals (EDCs) with hydrophilic hydroxyl groups and hydrophobic aromatic groups, has been widely used in plastic industries. The chemical waste from the industry is sometimes discharges into lakes and rivers, and then these surface waters can be polluted. So, this article aims to investigate the bio-sorption process of BPA by the inactivated lichen (Pseudoevernia furfuracea) biomass from aqueous solution. At initial, the effect of the variables such as initial BPA concentration, solution pH, temperature, contact time and recovery rate on the bio-sorption process was investigated. From the optimal results, it has been observed that the highest removal efficiency is approximately 64% at a contact time of 3-h, the bio-sorbent concentration of 9 mg/L, initial BPA concentration of 40 mg/L, and agitation speed of 150 rpm at pH 5.0. In explaining the bio-sorption potential of lichen biomass, Langmuir and/or Redlich-Peterson isotherms with two and three parameters, respectively were observed to be better fit with the experimental isotherm data (R2 = 0.982). From equilibrium data based on difference between the measured and predicted results (qe, exp and qe, pre), it was shown that biosorption of BPA could be best described by the pseudo second order kinetic model with minimum sum of square error of 2.61%. In addition, it shows more film diffusion, and partly pore diffusion in linearity region in terms of kinetic sorption behaviors of BPA in the rate-limiting step as well as intra-particle diffusion according to Boyd's kinetic model with better regression coefficient than 0.981 when compared to the other used kinetic models, including Bangham's pore diffusion and Elovich kinetic models (with R2 of 0.958 and 0.929). The thermodynamic studies showed that the biosorption process was spontaneous, and chemically feasible. Therefore, due to be low-cost, eco-friendly character, wide availability and easily accessible, the lichen biomass could be used as a promising bio-sorbent for the removal of BPA from the environment and wastewater effluents.

Removal of food dyes from aqueous solution by chitosan-vermiculite beads.

In this study, Chitosan (Ch)-Vermiculite (V) composite beads material which is a low-cost and naturally effective adsorbent were used for efficient removal of Sunset Yellow FCF (Sy) and Brilliant Blue FCF (Bb) food dyes from aqueous solution. Ch-V composite beads were characterized by using FTIR, SEM, XRD and PZC analysis. The adsorbent properties of Ch-V composite beads for Sy and Bb dyes were evaluated in terms of pH, concentration, kinetic (time) and thermodynamic (temperature) of adsorption. The experimental data presented were obtained from Langmuir, Freundlich and Dubinin-Radushkevich (DR) isotherm models. The maximum adsorption capacity for the Langmuir equation was found to be 0.387 mol kg-1 for Sy and 0.229 mol kg-1 for Bb, respectively. The results showed that the experimental data were better fit the Langmiur model for Sy and the Freundlich model for Bb. Adsorption energies obtained from DR model for Sy and Bb showed that adsorption processes were chemically. The pseudo-second order and intra-particle diffusion models of adsorption kinetics are in accordance with Sy and Bb. As a result of thermodynamic evaluation of Sy and Bb adsorption, it was found that adsorption processes were endothermic, entropy increased and reaction was spontaneous.

Assessment of Pb2+ removal capacity of lichen (Evernia prunastri): application of adsorption kinetic, isotherm models, and thermodynamics.

Biological materials play a significant role in the treatment of heavy metal-contaminated soil and wastewater. In this study, the Pb2+ biosorption potential of lichen Evernia prunastri, extensively available at a forest in Bilecik-Turkey, was investigated at batch-scale level. The optimal conditions were determined and the adsorption isotherms, kinetics, and thermodynamic calculations were also done. In order to have detailed knowledge about metal biosorption, SEM, FTIR, and BET analyses were carried out before and after the biosorption process. The optimal pH was found pH 4 and the maximum metal uptake capacity was found as 0.067 mol kg-1. The results of this study indicate that the lichen was effectively applied to the removal of Pb2+ process as an inexpensive biosorbent from industrial wastewater.

Effective UO22+ removal from aqueous solutions using lichen biomass as a natural and low-cost biosorbent.

The UO22+ biosorption properties of a lichen, Evernia prunastri, from aqueous solutions were investigated. The widely occurring lichen samples were collected from the forest in Bilecik-Turkey. The UO22+ biosorption onto lichen was characterized by FT-IR and SEM-EDX analysis techniques before and after biosorption. The effects of the solution pH, biosorbent dosage, UO22+ concentration, contact time, and temperature on UO22+ biosorption on lichen sample were studied by using the batch method. The isotherm experimental data were described using isotherm models of Langmuir, Freundlich and Dubinin Radushkevich. The maximum UO22+ biosorption capacity of the lichen sample was estimated by the Langmuir equation to be 0.270 mol kg-1. The adsorption energy from the Dubin Radushkevich model was found to be 8.24 kJ mol-1. Kinetic data determined that the biosorption was best described by the pseudo-second-order kinetic model. Thermodynamic findings showed that the biosorption process was endothermic, entropy increased and spontaneous. In conclusion, the lichen appears to be a promising biosorbent for the removal of UO22+ ions from aqueous solutions because of high biosorption capacity, easy usability, low cost, and high reusability performance.

Synthesis and characterization of a composite polymeric material including chelating agent for adsorption of uranyl ions.

In this study, a versatile polymeric material was synthesized by grafting Calcon Carboxylic Acid (CCA), which is known as a chelating agent for some metal ions, to polyacrylamide (PAA) structure. Thus, the adsorptive properties of inert PAA polymer were significantly improved owing to this procedure. The obtained new material, CCA-g-PAA, was characterized by point zero charge (PZC), FTIR, SEM, and UV-VIS-NIR analysis. The adsorption properties of new material were investigated comprehensively and experimental variables were optimized such as pH, temperature, time, and concentration. Experimental data were evaluated by using theoretical adsorption models. The maximum adsorption capacity of material was calculated as 0.079molkg-1 by considering Langmuir equation. The constants calculated from Freundlich and DR model were found as 6.98 and 0.441, respectively. Adsorption kinetic was also explained with pseudo second order and intra particular diffusion models. Experimental studies were showed that adsorption was endothermic and occurred spontaneously. The developed material has important advantages such as reusability, cost-effective synthesis procedure, high adsorption capacity, and selectivity.