Hybrid Sorbent Research Articles

Sb(III)-Imprinted Organic-Inorganic Hybrid Sorbent Prepared by Hydrothermal-Assisted Surface Imprinting Technique for Selective Adsorption of Sb(III)

Sb(III)-imprinted organic-inorganic hybrid sorbent was prepared by hydrothermal-assisted surface imprinting technique and was characterized by Fourier transform infrared spectroscopy, scanning electron microscopy coupled to an energy dispersive spectrometer and N2 adsorption/desorption isotherms. Hydrothermal-assisted process can improve the selectivity of the Sb(III)-imprinted hybrid sorbent for Sb(III) due to stable control of temperature and pressure. The Sb(III)-imprinted hybrid sorbent IIS indicated higher selectivity for Sb(III), had high static adsorption capacity of 37.3 mg g–1 for Sb(III), displayed stable adsorption capacity in pH range from 4 to 8, reached an rapid adsorption equilibrium within 30 min. According to the correlation coefficient (r2 > 0.99), the experimental data fitted better the pseudo-second-order kinetic model and Langmuir equilibrium isotherm.

Applications of magnetic hybrid adsorbent derived from waste biomass for the removal of metal ions and reduction of 4-nitrophenol

The use of industrial waste to synthesize materials of technological interest is a rational way to minimize or solve environmental pollution problems. This work investigates the adsorption of cadmium and lead ions by magnetic hybrid adsorbents synthesized using the in natura biomasses coconut mesocarp (CCFe), sawdust (SAFe), and termite nest (TEFe) for the organic phases and magnetic cobalt ferrite as the inorganic phase. The formation of a cobalt ferrite phase was confirmed by XRD. The use of XRD and FTIR analyses revealed the presence of organic matter in the structure of the material. Removal assays performed at different pH values (2.0–8.0) showed the effectiveness of the adsorbent for the removal of Pb2+ at pH 3.0 and Cd2+ at pH 4.0. The adsorption processes showed fast kinetics, with removal of 79–86% of Pb2+ and 49% of Cd2+ within only 5 min, and removal of 92–96% of the metal species at equilibrium. In the case of cadmium, the hybrid sorbents (CCFe, SAFe, and TEFe) showed high removal capacity after three reuse cycles, while the removal of lead decreased from 99% to 40%. The adsorbent matrices saturated with the recovered cadmium and lead ions showed excellent catalytic performance in the reduction of 4-nitrophenol, with 99.9% conversion within 43–56 s. The materials showed high capacities for reuse in three successive reduction cycles. The findings highlight the effectiveness of an industrial symbiosis approach to the development of new technologically important materials.

Sol-gel niobia sorbent with a positively charged octadecyl ligand providing enhanced enrichment of nucleotides and organophosphorus pesticides in capillary microextraction for online HPLC analysis.

A niobia-based sol-gel organic-inorganic hybrid sorbent carrying a positively charged C18 ligand (Nb2 O5 -C18 (+ve)) was synthesized to achieve enhanced enrichment capability in capillary microextraction of organophosphorus compounds (which include organophosphorus pesticides and nucleotides) before their online analysis by high-performance liquid chromatography. The sorbent was designed to simultaneously provide three different types of molecular level interactions: electrostatic, Lewis acid-base, and van der Waals interactions. To understand relative contributions of various molecular level analyte-sorbent interactions in the extraction process, two other sol-gel niobia sorbents were also created: (a) a purely inorganic sol-gel niobia sorbent (Nb2 O5 ) and (b) an organic-inorganic hybrid sol-gel niobia sorbent carrying an electrically neutral-bonded octadecyl ligand (Nb2 O5 -C18 ). The extraction efficiency of the created sol-gel niobia sorbent (Nb2 O5 -C18 (+ve)) was compared with that of analogously designed and synthesized titania-based sol-gel sorbent (TiO2 -C18 (+ve)), taking into consideration that titania-based sorbents present state-of-the-art extraction media for organophosphorus compounds. In capillary microextraction with high-performance liquid chromatography analysis, Nb2 O5 -C18 (+ve) had shown 40-50% higher specific extraction values (a measure of extraction efficiency) over that of TiO2 -C18 (+ve). Compared to TiO2 -C18 (+ve), Nb2 O5 -C18 (+ve) also provided superior analyte desorption efficiency (96vs. 90%) during the online release of the extracted organophosphorus pesticides from the sorbent coating in the capillary microextraction capillary to the chromatographic column using reversed-phase high-performance liquid chromatography mobile phase.

CO2 absorption and diffusion in ionic liquid [P66614][Triz] modified molecular sieves SBA-15 with various pore lengths

Mesoporous molecular sieves SBA-15 with four pore structures were loaded with an ionic liquid [P66614][Triz] to adsorb CO2 from raw biohythane. The hybrid sorbents of SBA-15 loaded with [P66614][Triz] were characterized by using N2 adsorption analyzer, thermogravimetric analyzer, scanning electron microscopy, and high-resolution transmission electron microscopy. The molecular sieve SBA-15 (with the most probable pore size of 4.3nm) loaded with 50% ionic liquid (IL), which was called SBA-15 (4.3) −50% IL, exhibited the fastest CO2 absorption rate and the shortest equilibrium time, which was approximately one-third of the equilibrium times of the other three hybrid sorbents. An intraparticle diffusion model was used to clarify that SBA-15 (4.3) −50% IL (with the shortest pore length of 120nm) executed a two-stage CO2 absorption process, which reduced the CO2 absorption time. The rate constant kI in the first stage of the CO2 absorption of SBA-15 (4.3) −50% IL was approximately four times as much as those of the other three hybrid sorbents because the cross-section area of its total pores was approximately three times higher than those of the other three hybrid sorbents. Results showed that pore length had significant effect on CO2 absorption performance.

Enhanced CO2 sorption efficiency in amine-functionalised 2D/3D graphene/silica hybrid sorbents.

Owing to the geometrical features of 2D graphene intercalated into 3D mesoporous silica, CO2 sorption increased by 51% and the heat of sorption reduced by up to 27% as compared to a pure 3D mesoporous silica sorbent without graphene. The superior performance of the amine-functionalised 2D/3D hybrid sorbent was attributed to the enhanced porosity and graphene physisorption at the expense of amine chemisorption.

Role of Pectin Substances in the Structural Organization of the Flax Fiber–Montmorillonite Hybrid Sorbent

The degree of immobilization of montmorillonite on flax fiber was determined experimentally, and the effect of the nonadditive increase in the sorption capacity of the biocomponent material was evaluated. Studies of pectin–montmorillonite model systems using methods of laser diffraction, X-ray diffraction, and gas adsorption revealed the formation of associate pairs with an equivalent increase in the pectin particle size, a threefold increase in the interlayer distance in the mineral structure, and a superadditive increase in the pore structure parameters. These effects prove formation of hybrid composites with limited intercalation of pectin polymer chains.

Capsule Phase Microextraction: The Total and Ultimate Sample Preparation Approach

Although analytical instrument has enjoyed unprecedented improvements in recent years, resulting in miniaturization, enhanced sensitivity, robust control systems as well as extended separation and detection capability, analytical and bioanalytical sample preparation still remain as the most challenging and time-consuming step in the analytical workflow. Collection of a representative sample is generally followed by a series of operations, collectively known as sample preparation and often include filtration, centrifugation, protein precipitation, analyte extraction, elution in organic solvent, solvent evaporation, and sample reconstitution. Many of these steps are carried out manually that ultimately prolongs the overall analysis time. Capsule Phase Microextraction (CPME), a green and new generation sample preparation technique, has been developed to streamline current state-of-the-art of sample preparation practices. It exploits the advanced material properties of inorganic-organic hybrid sorbents, integrates the filtration and sample diffusion mechanism into the device, and provides the independence of sample preparation both in the laboratory and in the field without sacrificing the convenience of the analyst and the quality of the analytical data. The article describes the development of CPME and explains its advantageous features to the current and future analytical chemists and separation scientists.

An efficient mercapto-functionalized organic-inorganic hybrid sorbent for selective separation and preconcentration of antimony(iii) in water samples.

This work reported on the application of mercapto-functionalized silica-supported organic–inorganic hybrid sorbent as a solid phase extraction (SPE) extractant for effective separation and preconcentration of Sb(iii) species in real water samples. The influences of pH, sorbent amounts, flow rates and the concentration of eluent on the adsorption and desorption of Sb(iii) species had been evaluated. The recovery of Sb(iii) species at pH 5 with 100 mg mercapto-functionalized hybrid sorbent at the flow rate of 5.0 mL min−1 was greater than 95% without interference from all of metal ions tested. The trapped Sb(iii) species by extractant was then eluted with 5% HCl solution at the flow rate of 5.0 mL min−1. The proposed procedure permitted large enrichment factors of about 200 and higher for 10 μg L−1 of Sb(iii) species. The merits of analytical figures for the determination of Sb(iii) species were as follows: detection limit (3σ, n = 11), 2 ng L−1; precision, 1.6% (n = 11) for 10 μg L−1 of Sb(iii) species; the linear calibration curve presented in the concentration range of 1.0–200.0 μg L−1. The validity of the proposed procedure was checked by the analysis of standard reference materials. Excellent agreement between the analytical results and the certified values (t-test at 95% confidence level) was found. The mercapto-functionalized hybrid sorbent as a SPE extractant was applied to the determination of Sb(iii) species in various water samples with satisfactory results.

Zinc Ion Removal on Hybrid Pectin-Based Beads Containing Modified Poly(Methyl Methacrylate) Waste.

A new hybrid sorbent in the form of round beads containing modified poly(methyl methacrylate) (PMMA) waste immobilized in pectin and crosslinked with calcium ions was prepared. A previously obtained and characterized powdered poly(methyl methacrylate)–based sorbent was used. Batch and column studies on the new material’s sorption-desorption properties were performed. Two kinetic models (pseudo-first- and pseudo-second-order) and three isotherms (Langmuir, Langmuir bisite and Freundlich) were used to describe the results. Breakthrough and elution curves were also obtained. Nitric, hydrochloric, and sulfuric acid of various concentrations were used in the desorption studies. Higher sorption affinity of zinc(II) ions to hybrid sorbent than to pectin alone, reflected by higher values of the Langmuir and Freundlich model parameters, was observed. The maximum sorption capacities, calculated based on the best-fitted models, were 50.2 mg/g (Langmuir bisite) and 42.2 mg/g (Langmuir) for hybrid and only pectin beads, respectively. The stripping of Zn ions using 0.1 M solutions of mineral acids was similarly effective in the case of both sorbents. The mass balance calculated for the column studies showed about 100% recovery of zinc in a sorption-desorption cycle. By applying the hybrid sorbent under the studied conditions it is possible to purify Zn in water to the level permitted by law and concentrate Zn(II) ions by about 60 times.

Advances in organic-inorganic hybrid sorbents for the extraction of organic and inorganic pollutants in different types of food and environmental samples.

The efficiency of the extraction and removal of pollutants from food and the environment has been an important issue in analytical science. By incorporating inorganic species into an organic matrix, a new material known as an organic-inorganic hybrid material is formed. As it possesses high selectivity, permeability, and mechanical and chemical stabilities, organic-inorganic hybrid materials constitute an emerging research field and have become popular to serve as sorbents in various separaton science methods. Here, we review recent significant advances in analytical solid-phase extraction employing organic-inorganic composite/nanocomposite sorbents for the extraction of organic and inorganic pollutants from various types of food and environmental matrices. The physicochemical characteristics, extraction properties, and analytical performances of sorbents are discussed; including morphology and surface characteristics, types of functional groups, interaction mechanism, selectivity and sensitivity, accuracy, and regeneration abilities. Organic-inorganic hybrid sorbents combined with extraction techniques are highly promising for sample preparation of various food and environmental matrixes with analytes at trace levels.

Tantala-based sol-gel coating for capillary microextraction on-line coupled to high-performance liquid chromatography

A sol-gel organic-inorganic hybrid sorbent, consisting of chemically integrated tantalum (V) ethoxide (TaEO) and polypropylene glycol methacrylate (PPGM), was developed for capillary microextraction (CME). The sol-gel sorbent was synthesized within a fused silica capillary through hydrolytic polycondensation of TaEO and chemical incorporation of PPGM into the evolving sol-gel tantala network. A part of the organic-inorganic hybrid sol-gel network evolving in the vicinity of the capillary walls had favorable conditions to get chemically bonded to the silanol groups on the capillary surface forming a surface-bonded coating. The newly developed sol-gel sorbent was employed to isolate and enrich a variety of analytes from aqueous samples for on-line analysis by high-performance liquid chromatography (HPLC) equipped with a UV detector. CME was performed on aqueous samples containing trace concentrations of analytes representing polycyclic aromatic hydrocarbons, ketones, alcohols, amines, nucleosides, and nucleotides. This sol-gel hybrid coating provided efficient extraction with CME-HPLC detection limits ranging from 4.41pM to 28.19 pM. Due to direct chemical bonding between the sol-gel sorbent coating and the fused silica capillary inner surface, this sol-gel sorbent exhibited enhanced solvent stability. The sol-gel tantala-based sorbent also exhibited excellent pH stability over a wide pH range (pH 0–pH 14). Furthermore, it displayed great performance reproducibility in CME-HPLC providing run-to-run HPLC peak area relative standard deviation (RSD) values between 0.23% and 3.83%. The capillary-to-capillary RSD (n=3), characterizing capillary preparation method reproducibility, ranged from 0.24% to 4.11%. The results show great performance consistency and application potential for the sol-gel tantala-PPGM sorbent in various fields including biomedical, pharmaceutical, and environmental areas.

Valorisation of N and P from waste water by using natural reactive hybrid sorbents: Nutrients (N,P,K) release evaluation in amended soils by dynamic experiments

The removal of nutrients (nitrogen (N), phosphorous (P)) from waste water has become a resource recovery option in recent regulations worldwide, as observed in the European Union. Although both of these nutrients could be recovered from the sludge line, >70–75% of the N and P is discharged into the water line. Efforts to improve the nutrient recovery ratios have focused on developing low-cost technologies that use sorption processes. In this study, a natural zeolite (clinoptilolite type) in its potassium (K) form was impregnated with hydrated metal oxides and used to prepare natural hybrid reactive sorbents (HRS) for the simultaneous recovery of ammonium (NH4+) and phosphate (PO43−) from treated urban waste water. Three unfertile soils (e.g., one acidic and two basic) amended with N-P-K charged HRS were leached with deionized water (e.g. to simulate infiltration in the field) at two- and three-day time intervals over 15 different leaching cycles (equivalent to 15 bed volumes). The N-P-K leaching profiles for the three charged hybrid sorbents exhibited continuous nutrient release, with their values dependent on the composition of minerals in the soils. In the basic soil that is rich in illite and calcite, the release of potassium (K+) and ammonium (NH4+) is favoured by-ion exchange with calcium (Ca2+) and accordingly diminishes the release of phosphate (PO43−) due to its limited solubility in saturated calcite solutions (pH8 to 9). The opposite is true for sandy soils that are rich in albite (both acidic and basic), whereas the release of NH4+ and K+ was limited and the values of both ions measured in the leaching solutions were below 1mg/L. Their leaching solutions were poor in Ca2+, and the release of PO43− was higher (up to 12mgP-PO43−/L). The nutrient releases necessary for plant growth were provided continuously and were controlled primarily by the soil mineral dissolution rates fixing the soil aqueous solution composition (e.g. pH and ionic composition; in particular, the presence of calcite is a determinant for nutrient release, especially in alkaline soils). The N-P-K charged HRS sorbents that were used for soil amendment may be an alternative for avoiding nutrient leaching and reaching the goals of soil sustainability in agriculture and reducing the nutrient overloading of surface waters.

Immobilization of in-situ formed Ni(OH)2 nanoparticles in chitosan beads for efficient removal of U(VI) from aqueous solutions

Both metal hydroxides and chitosan have been recognized as effective scavengers for nuclide ions. However, the aggregation of metal hydroxides and the weak mechanical strength of chitosan beads greatly restricts their application. Herein, the in-situ formed Ni(OH)2 nanoparticles was immobilized in chitosan matrix to obtain a novel hybrid sorbent (CSNi) for U(VI) adsorption. The CSNi showed high affinity for U(VI) sorption, with the inner-sphere complexation as the main mechanism. The maximum mono-layer adsorption capacity for U(VI) at 298 K reached 164.2 mg/g. The U(VI) sorption was endothermic and spontaneous, and kinetically followed the pseudo-second-order model. These findings highlight the possibility of using CSNi for efficient removal of U(VI) from wastewater.

Complex-Emulsion synthesis of organo-inorganic amphiphilic sorbents with specific affinity for glucose

Granular organo-inorganic amphiphilic sorbents with specific affinity for glucose were synthesized with the aim of developing selective hemosorbents for efferent therapy of hyperglycemia. The sorbents were prepared in oil/water/oil complex emulsions by copolymerization of 2-hydroxyethyl methacrylate and ethylene glycol dimethacrylate on the surface of selenium nanoparticles stabilized with polyvinylpyrrolidone. The phases were stabilized with excess selenium/polyvinylpyrrolidone nanocomplexes. Optimum synthesis conditions ensuring formation of hybrid sorbents with the physicochemical properties required for performing efficient preparative hemosorption and plasma adsorption processes were found. The specific affinity for glucose was reached by modification of these sorbents via imprinting with template glucose molecules in the surface polymer layer and via introduction of boric acid as an affine ligand into the hybrid matrices.

Fabric Sol–gel Phase Sorptive Extraction Technique: A Review

Since the introduction in 2014 of fabric phase sorptive extraction (FPSE) as a sample preparation technique, it has attracted the attention of many scientists working in the field of separation science. This novel sorbent extraction technique has successfully utilized the benefits of sol–gel derived hybrid sorbents and a plethora of fabric substrates, resulting in a highly efficient, sensitive and green sample pretreatment methodology. The proposed procedure is an easy and efficient pathway to extract target analytes from different matrices providing inherent advantages such as high sample loading capacity and short pretreatment time. The present review mainly focuses on the background and sol–gel chemistry for the preparation of new fabric sorbents as well as on the applications of FPSE for extracting target analytes, from the time that it was first introduced. New modes of FPSE including stir FPSE, stir-bar FPSE, dynamic FPSE, and automated on-line FPSE are also highlighted and commented upon in detail. FPSE has been effectively applied for the determination of various organic and inorganic analytes in different types of environmental and biological samples in high throughput analytical, environmental, and toxicological laboratories.

Column adsorption of Cu(II) by polymer-supported nano-iron oxides in the presence of sulfate: Experimental and mathematical modeling

Abstract Polymer-supported hydrous iron oxides (HFOs) are promising for heavy metals removal from aqueous systems. The ubiquitous inorganic ligands, e.g., sulfate, are expected to exert considerable impacts on pollutants removal by these hybrid sorbents. Herein, we obtained a hybrid sorbent HFO-PS by encapsulating nanosized HFO into macroporous polystyrene (PS) resin. Both batch and column sorption experiments of Cu(II) by HFO-PS were carried out in the presence of sulfate. Obviously, the presence of sulfate is favorable for Cu(II) sorption onto HFO-PS. The performances of column Cu(II) removal were fitted and predicted with Adams–Bohart, Clark, Thomas and BDST models. Thomas model is suggested best-fit to predict the breakthrough curves. Besides, a linear correlation is observed between breakthrough time and column length based on BDST model, which might be useful for predicting the breakthrough time for Cu(II) removal by HFO-PS.

Silica- and germania-based dual-ligand sol-gel organic-inorganic hybrid sorbents combining superhydrophobicity and π-π interaction. The role of inorganic substrate in sol-gel capillary microextraction

Principles of sol-gel chemistry were utilized to create silica- and germania-based dual-ligand surface-bonded sol-gel coatings providing enhanced performance in capillary microextraction (CME) through a combination of ligand superhydrophobicity and π-π interaction. These organic-inorganic hybrid coatings were prepared using sol-gel precursors with bonded perfluorododecyl (PF-C12) and phenethyl (PhE) ligands. Here, the ability of the PF-C12 ligand to provide enhanced hydrophobic interaction was advantageously combined with π-π interaction capability of the PhE moiety to attain the desired sorbent performance in CME. The effect of the inorganic sorbent component on microextraction performance of was explored by comparing microextraction characteristics of silica- and germania-based sol-gel sorbents. The germania–based dual-ligand sol-gel sorbent demonstrated superior CME performance compared to its silica-based counterpart. Thermogravimetric analysis (TGA) of the created silica- and germania-based dual-ligand sol-gel sorbents suggested higher carbon loading on the germania-based sorbent. This might be indicative of more effective condensation of the organic ligand-bearing sol-gel-active chemical species to the germania-based sol-gel network (than to its silica-based counterpart) evolving in the sol solution. The type and concentration of the organic ligands were varied in the sol-gel sorbents to fine-tune extraction selectivity toward different classes of analytes. Specific extraction (SE) values were used for an objective comparison of the prepared sol-gel CME sorbents. The sorbents with higher content of PF-C12 showed remarkable affinity for aliphatic hydrocarbons. Compared to their single-ligand sol-gel counterparts, the dual-ligand sol-gel coatings demonstrated significantly superior CME performance in the extraction of alkylbenzenes, providing up to ∼65.0% higher SE values. The prepared sol-gel CME coatings provided low ng L−1 limit of detections (LOD) (4.2–26.3 ng L−1) for environmentally important analytes including polycyclic aromatic hydrocarbons, ketones and aliphatic hydrocarbons. In CME-GC experiments (n = 5), the capillary-to-capillary RSD value was ∼2.1%; such a low RSD value is indicative of excellent reproducibility of the sol-gel method used for the preparation of these CME coatings. The dual-ligand sol-gel coating provided stable performance in capillary microextraction of analytes from saline samples.

Highly Efficient Removal of Dye from Water Using Magnetic Carrageenan/Silica Hybrid Nano-adsorbents

The discharge of effluents containing organic dyes extensively used in the industry is a matter of concern because these pollutants can cause harmful effects in the environment and human health. In this work, magnetic iron oxide nanoparticles coated with κ-carrageenan/silica organic/inorganic hybrid shells were synthesized and used as novel adsorbents for the magnetically assisted removal of methylene blue (MB) from water. The kinetics of adsorption was well predicted using the pseudo-second-order equation. These hybrid materials exhibited high adsorption capacity (530 mg/g maximum) that could be ascribed to surfaces enriched with ester sulfate groups due to extensive grafting of κ-carrageenan over the siliceous domains by using a new surface modification method. The sorbents were long-term colloidal stable and could be easily regenerated after rinsing with KCl aqueous solution. The MB removal efficiency over six consecutive adsorption/desorption cycles was above 97%, which demonstrates the reusability potential and robustness of these hybrid sorbents. This is a new type of adsorbent that promises extensive application in the removal of organic dyes from wastewaters using magnetic separation technologies.

Fabric phase sorptive extraction of selected penicillin antibiotic residues from intact milk followed by high performance liquid chromatography with diode array detection.

Fabric phase sorptive extraction (FPSE), a novel sorbent-based microextraction method, was evaluated as a simple and rapid strategy for the extraction of four penicillin antibiotic residues (benzylpenicillin, cloxacillin, dicloxacillin and oxacillin) from cows' milk, without prior protein precipitation. Time-consuming solvent evaporation and reconstitution steps were eliminated successfully from the sample preparation workflow. FPSE utilizes a flexible fabric substrate, chemically coated with sol-gel derived, highly efficient, organic-inorganic hybrid sorbent as the extraction medium. Herein short-chain poly(ethylene glycol) provided optimum extraction sensitivity for the selected penicillins, which were analysed using an RP-HPLC method, validated according to the European Decision 657/2002/EC. The limit of quantitation was 10μg/kg for benzylpenicillin, 20μg/kg for cloxacillin, 25μg/kg dicloxacillin and 30μg/kg oxacillin. These are a similar order of magnitude with those reported in the literature and (with the exception of benzylpenicillin) are less than the maximum residue limits (MRL) set by European legislation.

New polymeric/inorganic hybrid sorbents based on red mud and nanosized magnetite for large scale applications in As(V) removal

Red mud (RM), a waste product generated in the industrial production of aluminium, was recovered for a second use as As(V) adsorbent. RM adsorption properties were compared to those obtained with a nanostructured in-lab synthesized iron oxide, magnetite. Operational problems associated with powdery consistency of raw materials were solved with the synthesis of new polymeric/inorganic hybrid sorbents by dispersing red mud and magnetite in chitosan. The behaviour of raw red mud and magnetite towards As(V) adsorption has been critically compared with that observed for the hybrid materials. pH dependence studies demonstrated that near neutral environments favour As(V) elimination. The sorption kinetics for the iron oxides showed that equilibrium was reached in less than 3h for raw materials and up to 15h for immobilized red mud and magnetite. The amount of arsenic sorbed on the four different sorbents as a function of the equilibrium arsenic concentration has been fitted to a Freundlich isotherm and a multilayer adsorption mechanism is proposed. Finally, continuous flow experiments were developed using chitosan immobilized red mud. Results allowed selecting batch conformation as the most effective for As(V) removal.