Removal of Azo Dyes from Water Using Natural Luffa cylindrica as a Non-Conventional Adsorbent.

Reducing high concentrations of pollutants such as heavy metals, pesticides, drugs, and dyes from water is an emerging necessity. We evaluated the use of Luffa cylindrica (Lc) as a natural non-conventional adsorbent to remove azo dye mixture (ADM) from water. The capacity of Lc at three different doses (2.5, 5.0, and 10.0 g/L) was evaluated using three concentrations of azo dyes (0.125, 0.250, and 0.500 g/L). The removal percent (R%), maximum adsorption capacity (Qm), isotherm and kinetics adsorption models, and pH influence were evaluated, and Fourier-transform infrared spectroscopy and scanning electron microscopy were performed. The maximum R% was 70.8% for 10.0 g L-1Lc and 0.125 g L-1 ADM. The Qm of Lc was 161.29 mg g-1. Adsorption by Lc obeys a Langmuir isotherm and occurs through the pseudo-second-order kinetic model. Statistical analysis showed that the adsorbent dose, the azo dye concentration, and contact time significantly influenced R% and the adsorption capacity. These findings indicate that Lc could be used as a natural non-conventional adsorbent to reduce ADM in water, and it has a potential application in the pretreatment of wastewaters.

Enhanced artificial intelligence for electrochemical sensors in monitoring and removing of azo dyes and food colorant substances.

It is necessary to determine whether synthetic dyes are present in food since their excessive use has detrimental effects on human health. For the simultaneous assessment of tartrazine and Patent Blue V, a novel electrochemical sensing platform was developed. As a result, two artificial azo colorants (Tartrazine and Patent Blue V) with toxic azo groups (-NN-) and other carcinogenic aromatic ring structures were examined. With a low limit of detection of 0.06 µM, a broad linear concentration range 0.09µM to 950µM, and a respectable recovery, scanning electron microscopy (SEM) was able to reveal the excellent sensing performance of the suggested electrode for patent blue V. The electrochemical performance of an electrode can be characterized using cyclic and differential pulse voltammetry, and electrochemical impedance spectroscopy. Moreover, the classification model was created by applying binary classification assessment using enhanced artificial intelligence comprises of support vector machine (SVM) and Genetic Algorithm (GA), respectively, a support vector machine and a genetic algorithm, which was then validated using the 50 dyes test set. The best binary logistic regression model has an accuracy of 83.2% and 81.1%, respectively, while the best SVM model has an accuracy of 90.3% for the training group of samples and 81.1% for the test group (RMSE = 0.644, R2 = 0.873, C = 205.41, and = 5.992). According to the findings, Cu-BTC MOF (copper (II)-benzene-1,3,5-tricarboxylate) has a crystal structure and is tightly packed with hierarchically porous nanomaterials, with each particle's edge measuring between 20 and 37 nm. The suggested electrochemical sensor's analytical performance is suitable for foods like jellies, condiments, soft drinks and candies.

QuEChERS sample preparation integrated to dispersive liquid-liquid microextraction based on solidified floating organic droplet for spectrometric determination of sudan dyes: A synergistic approach.

In this project, a synergistic approach has been proposed where a quick, easy, cheap, effective, rugged, and safe (QuEChERS) sample preparation technique was developed for the extraction of sudan III and sudan IV dyes in different spices prior to its dispersive liquid-liquid microextraction based on solidified floating organic droplet (DLLME-SFO). Initially, the sample was extracted by QuEChERS method and then preconcentrated through DLLME-SFO followed by spectrophotometric detection. All the experimental parameters i.e., volume of extraction solvent, pH, acetonitrile to water ratio, temperature, centrifugation rate and time, and sample volume were optimized. Limit of detection (LOD) calculated for sudan III and sudan IV were 0.42 and 0.35 mg/L, respectively. Excellent recoveries were obtained in the range of 98.29-99.88%. After validation through standard addition methodology, the developed QuEChERS@DLLME-SFO method was successfully applied to determine sudan (III-IV) dyes in real spices samples. Integration of QuEChERS and DLLME-SFO was found to be a suitable substitute to eliminate the usage of costly primary secondary amines and other sorbents. The synergistic approach of QuEChERS and DLLME-SFO with the aid of UV/visible spectrophotometry makes it prompt, cost effective technique with excellent analytical figures of merit.

The Removal of Binary Mixture of Dyes by Heterogeneous Fenton Oxidation: Kinetics, Product Identification and Toxicity Assessment.

The removal of mixture of two azo dyes, Acid blue 29 and Ponceau xylidine, was studied by heterogeneous Fenton and Fenton-type processes using hydrogen peroxide and sodium persulphate as oxidants in the presence of and nano and micro- particles as catalysts. The synthesised nano- particles were characterised using analytical techniques viz. FT-IR, TEM, EDX, powder XRD and VSM. We have examined the effects of particle size on the COD removal efficiency and the reusability of the catalyst after optimising pH, and concentrations of catalyst and oxidant. Combination of nano-  and hydrogen peroxide possessed higher COD removal efficiency, which was accelerated in acidic pH and inhibited at pH > 6. Total consumption of hydrogen peroxide confirmed the efficiency of the optimised parameters. The mechanism of the formation of intermediate ions and products are proposed. COD removal and consumption of hydrogen peroxide follow pseudo-first-order kinetics. The toxicity of the solutions was assessed using Aliivibrio fischeri light loss and Escherichia coli growth inhibition assays. Both the assays showed different toxicity levels for the same solution.

Volatile Nitrogenous Compounds from Bacteria: Source of Novel Bioactive Compounds.

Bacteria can produce nitrogenous compounds via both primary and secondary metabolic processes. Many bacterial volatile nitrogenous compounds produced during the secondary metabolism have been identified and reported for their antioxidant, antibacterial, antifungal, algicidal and antitumor activities. The production of these nitrogenous compounds depends on several factors, including the composition of culture media, growth conditions, and even the organic solvent used for their extraction, thus requiring their identification in specific conditions. In this review, we describe the volatile nitrogenous compounds produced by bacteria especially focusing on their antimicrobial activity. We concentrate on azo-compounds mainly pyrazines and pyrrolo-pyridines reported for their activity against several microorganisms. Whenever significant, extraction and identification methods of these compounds are also mentioned and discussed. To the best of our knowledge, this is first review describing volatile nitrogenous compounds from bacteria focusing on their biological activity.

Glutaraldehyde-cross-linked chitosan-alginate composite for organic dyes removal from aqueous solutions.

We present an approach for synthesis of a micro-porous composite of two well-known biopolymers, namely chitosan and alginate, using glutaraldehyde as the cross-linking agent. Alginate and chitosan were pre-treated before being mixed, and the two biopolymers' proportions were also monitored. Chitosan was modified using aniline with the help of formaldehyde crosslinker and then the twizer was further crosslinked with alginate using glutaraldehyde. The synthesized composite, glutaraldehyde cross-linked chitosan-alginate composite [(Cs-F-An)-G-Al] was characterized using spectral techniques and employed as a potential adsorbent for three dyes namely Brilliant green, Methyl orange and Patent Blue V. The pHPZC of the material was 7.5 and the maximum monolayer adsorption capacity (Qmax) was found to be 235.82, 198.09 and 117.34 mg g-1 for BG (at pH 8.0), MO (at pH 6.0) and PBV (at pH 3.0) respectively. It was found that the adsorption process follows a Freundlich adsorption isotherm and pseudo second order kinetics. A thermodynamic study revealed that the process of adsorption was enthalpy-driven and spontaneous in nature. Interestingly, the values of the adsorption capacity obtained in column adsorption method are in close agreement with those obtained in batch adsorption experiments, which shows the potential of the synthesized composite for uptake of dyes.

Nitrate modulation of Bacillus sp. biofilm components: a proposed model for sustainable bioremediation.

The presence of different pollutants in wastewater hinder microbial growth, compromise enzymatic activity or compete for electrons required for bioremediation pathway. Therefore, there is a need to use a single microorganism that is capable of tolerating different toxic compounds and can perform simultaneous bioremediation. In the present study, nitrate reducing bacteria capable of decolorizing azo dye was identified as Bacillus subtillis sp. DN using protein profiling, morphological and biochemical tests X-ray diffraction pattern, Raman spectroscopy and cyclic voltammetry confirm that the bacterium under study possesses membrane-bound nitrate reductase and that is capable of direct electron transfer. The addition of nitrate concentrations (0-50 mM) resulted in increased biofilm formation with variable exopolysaccharides, protein, and eDNA. Fourier Transform Infrared spectrum revealed the presence of a biopolymer at high nitrate concentrations. Effective capacitance and conductivity of the cells grown in different nitrate concentrations suggest changes in the relative position of polar groups, their relative orientation and permeability of cell membrane as detected by dielectric spectroscopy. The increase in biofilm shifted the removal of the azo dye from biodegradation to bioadsorption. Our results indicate that nitrate modulates biofilm components. Bacillus sp. DN granular biofilm can be used for simultaneous nitrate and azo dye removal from wastewater.

Fly ash modified magnetic chitosan-polyvinyl alcohol blend for reactive orange 16 dye removal: Adsorption parametric optimization.

A magnetic biocomposite blend of chitosan-polyvinyl alcohol/fly ash (m-Cs-PVA/FA) was developed by adding fly ash (FA) microparticles into the polymeric matrix of magnetic chitosan-polyvinyl alcohol (m-Cs-PVA). The effectiveness of m-Cs-PVA/FA as an adsorbent to remove textile dye (reactive orange 16, RO16) from aquatic environment was evaluated. The optimum adsorption key parameters and their significant interactions were determined by Box-Behnken Design (BBD). The analysis of variance (ANOVA) indicates the significant interactions can be observed between m-Cs-PVA/FA dose with solution pH, and m-Cs-PVA/FA dose with working temperature. Considering these significant interactions, the highest removal of RO16 (%) was found 90.3% at m-Cs-PVA/FA dose (0.06 g), solution pH (4), working temperature (30 °C), and contact time (17.5 min). The results of adsorption kinetics revealed that the RO16 adsorption was better described by the pseudo-second-order model. The results of adsorption isotherm indicated a multilayer adsorption process as well described by Freundlich model with maximum adsorption capacity of 123.8 mg/g at 30 °C. An external magnetic field can be easily applied to recover the adsorbent (m-Cs-PVA/FA). The results supported that the synthesized m-Cs-PVA/FA presents itself as an effective and promising adsorbent for textile dye with preferable adsorption capacity and separation ability during and after the adsorption process.

New and efficient NiO/chitosan/polyvinyl alcohol nanocomposites as antibacterial and dye adsorptive films.

The development of composite films with enhanced antibacterial and dye decolorization properties for water treatment has attracted a great attention. In this study, nickel oxide/chitosan/polyvinyl alcohol nanocomposite films containing different weight percentage of NiO nanoparticles with a dual functionality, removal of toxic dye and antibacterial properties, were prepared. Methyl orange (MO) was selected as a target pollutant. Additionally, the antimicrobial activity of the films against two Gram positive bacteria (Staphylococcus aureus and Bacillus cereus) and two Gram negative bacteria (Escherichia coli and Salmonella Typhimurium) was studied. The prepared samples were characterized by XRD, HRTEM, FESEM, ATR-FTIR, UV-Vis spectroscopy, and dielectric measurements. The morphological examination proved that the nanocomposite film has more porous structure compared to the unmodified chitosan/PVA. The antimicrobial tests indicated that the modified chitosan/PVA films have higher activity than pure chitosan/PVA toward all the tested pathogenic bacteria. The impact of the NiO amount (0.5, 1.5, 3, and 5 wt%), contact time (0-150 min), and adsorbent dose (40, 80, and 100 mg) on the removal of MO was studied. Dye adsorption results proved that the incorporation of 5 wt% NiO led to more than 2 fold increase in the dye removal percentage in comparison with the unmodified PVA/chitosan film.

Synthesis and characterization of chitosan/polyacrylamide hydrogel grafted poly(N-methylaniline) for methyl red removal.

Chitosan/polyacrylamide hydrogel grafted poly(N-methylaniline) (CS/PACM-gr-PNMA) was good synthesized by chemical oxidative radical polymerization using potassium persulphate (KPS). The obtained polymer samples are characterized using IR and Uv-visible spectroscopy. Both surface properties and thermal stability were studied using XRD, SEM, BET and TGA techniques respectively. The characterized polymeric samples were used as a new sorbent for methyl red (MR). MR as an example of azo-dyes presence as pollutants in industrial wastewater which cause physiological damages was chosen to uptake. The influence of contact time, adsorbent dose, and temperature on the efficiency of CS/PACM-gr-PNMA towards the removal of MR was investigated. The efficacy was equal to 98% through 120 min at room temperature. The obtained data show that, ∆H = -21.478 kJ mol-1, so adsorption process is physically spontaneous and follow Freundlich isotherm. The sorption process of MR on the surface of CS/PACM-gr-PNMA is proceed via the Lagergren pseudo-second order reaction. This confirms the removal mechanism by both chemical and physical adsorption of MR with both unpaired and π electrons present in polymer structure on NH, NH2, and benzene or quinoid units respectively. In addition, it can explain the chemical adsorption type which occurs through sharing between the used adsorbent materials and the dissolved materials beside the physical adsorption.

Functional chitosan/glycidyl methacrylate-based cryogels for efficient removal of cationic and anionic dyes and antibacterial applications.

In this study, we constructed a novel family of chitosan-based cryogels with antibacterial activity to treat different types of dye wastewater. Glycidyl methacrylate (GMA) cross-linked chitosan (CS) cryogels functionalized with negatively and positively molecules were prepared via thermo-crosslinking and freeze-drying methods. These chitosan-based cryogels present a well-defined three-dimensional microporous network structure with ultra-light and high porosity, and have high water absorption ability. For CS/GMA/SMA cryogels, 71.20% of Cationic Yellow X-8GL (CY) can be removed, and the process kinetics well corresponded to the Pseudo-second order model and Freundlich model. The quantity and percent of Reactive Yellow B-4RFN (RY) removal by CS/GMA/DMC cryogel reached at 224.6 mg/g and 96.11%, which closely fitted the Pseudo-second order model and Dubinin-Radushkevich isotherm. Furthermore, the chitosan-based cryogels showed antibacterial efficacies against E. coli and S. aureus. The prepared chitosan-based cryogels with adsorption and antibacterial properties have great potential for the remediation of dyeing wastewater.

3D porous bioadsorbents based on chitosan/alginate/cellulose nanofibers as efficient and recyclable adsorbents of anionic dye.

Natural polysaccharides are attractive materials for fabrication of eco-friendly biodsorbents for efficient water remediation. However, scarcity of adsorbents that possess features of high stability and adsorption capacity at various pH conditions, low-cost, eco-friendly, and recycleability at the same time still remains a great challenge. Herein, porous ionically crosslinked biofoams were prepared by freeze-drying of chitosan (CS)/sodium alginate (SA) complex (CSA). FTIR and XRD were used to characterize the structure of the bioadsorbents. SEM observations revealed that adsorbents have a 3D interconnected porous structure, which is a favorable morphology for dye adsorption. Accordingly, CSA and its nanocomposite containing 15 wt% cellulose nanofibers (CSAC15) exhibited a fast and efficient adsorption behavior with qm values of 2015 and 2297 mg/g for adsorption of the Eriochrome black-T (EBT) anionic dye, respectively, which are quite outstanding among the developed EBT adsorbents in the literature so far. The CSAC15 preserved its stability and high adsorption capacity at various pH solutions. The adsorption of EBT onto the bioadsorbents was well-described with the pseudo-second order kinetics and Freundlich isotherm. The proposed CSAC15 bioadsorbent featured repeated dye removal capability after five cycles of adsorption.

Adsorption, kinetics and thermodynamics studies of methyl orange dye sequestration through chitosan composites films.

Different films comprising pure chitosan (CS) and chitosan coated sodium zeolites composites films designated as CSZ1, CSZ2, CSZ3 and CSZ4 respectively are presented here for the sequestration of MO dye. The as-synthesized films were characterized by using FSESM, XPS XRD, and TGA analysis. The sequestration of methyl orange dye (MO) was studied under various adsorption parameters i.e. pH effect, reaction temperature, catalytic dosage, interaction period, and original dye concentration in batch experiments. The adsorption power of MO dye sequestration in the presence of CSZ3 was 287 mg g-1 higher than the fine CS (201 mg g-1), and lowest for CSZ4 (173 mg g-1). The experimental data is fitted in the pseudo-second order of chemical kinetics. The Freundlich and Langmuir adsorption models were used on behalf of the analysis of experimental data that revealed multilayered adsorption of MO dye. Kinetics, equilibrium and thermodynamic process were discussed in detailed, suggesting the endothermic and spontaneous process of the adsorption of MO dye on the exterior of films. The present work is general for the MO adsorption, however, it can be applied on large scale applications and can be easily adjustable in the water purification assemblies.

Azodyrecins A-C: Azoxides from a Soil-Derived Streptomyces Species.

Azoxy compounds belong to a small group of natural products sharing a common functional group with the general structure RN = N+(O-)R. Three new azoxides, azodyrecins A-C (1-3), were isolated from a soil-derived Streptomyces sp. strain P8-A2. The cis-alkenyl unit in 1-3 was found to readily isomerize to the trans-congeners (4-6). The structures of the new compounds were determined by detailed spectroscopic (1D/2D NMR) and HRMS data analysis. Azodyrecins belong to a new class of natural azoxy compounds and are proposed to derive from l-alanine and alkylamines. The absolute configurations of 1-6 were defined by comparison of ECD spectra. While no antimicrobial effects were observed for 1 against Staphylococcus aureus, Vibrio anguillarum, or Candida albicans, azodyrecin B (2) exhibited cytotoxicity against the human leukemia cell line HL-60 with an IC50 value of 2.2 µM.

Efficient carbon interlayed magnetic chitosan adsorbent for anionic dye removal: Synthesis, characterization and adsorption study.

The present paper describes the synthesis of a novel magnetic chitosan (CCF), in which the carbon-Fe3O4 core-shell nanoparticles play the role of magnetic part. The structure, property and morphology of the magnetic CCF were characterized by FT-IR, XRD, EDAX, SEM and BET techniques. Its adsorption performance was investigated for the removal of methyl orange from aqueous solutions by varying experimental conditions. The results showed the fast adsorption of methyl orange in wide pH range of 3-11 and the maximum adsorption capacity was found to be 425 mg g-1 at 45 °C. The results of adsorption kinetics indicated that the adsorption mechanism was better described by the pseudo-second-order equation, whereas pore diffusion is the rate-controlling of adsorption kinetics. Furthermore, among different isotherm models, Langmuir and Sips isotherm models fitted well the equilibrium experimental data at different temperatures revealing the surface heterogeneity of the adsorbents. The adsorbent exhibited high adsorption performance, compared to the some other chitosan adsorbents reported in literatures.

Removal of Brilliant Red dye (Brilliant Red E-4BA) from wastewater using novel Chitosan/SBA-15 nanofiber.

An environmental-friendly adsorbent composed of chitosan nanofibers modified by mesoporous silica sieve (CTS-SBA-15) was synthesized via an electrospinning technique and used to remove of brilliant Red dye from a wastewater solution. Characterization of the synthesized nanofibers using Fourier transform infrared (FT-IR), X-ray diffraction (XRD) and transmission electron microscopy (TEM) analyses revealed that the chitosan nanofibers were effectively modified with mesoporous silica sieve (SBA-15). The effects of some adsorption parameters such as pH, adsorbent dosage, and the time of adsorption process on the dye removal percentage were investigated in detail. Based on the kinetic and thermodynamic studies, the adsorption process obeyed the pseudo-second order and Langmuir models, respectively. The obtained results revealed that the dye removal efficiency of CTS-SBA-15 was about 98% in the presence of 0.03 g of the adsorbent and pH = 7 after 80 min. So, it was found that CTS-SBA-15 can act as inexpensive and efficient adsorbent for the brilliant Red E-4BA elimination from the contaminated water.

Chemical constituents from wetland soil fungus Penicillium oxalicum GY1.

A new azo compound, penoxalin (1), a new isochroman carboxylic acid, penisochroman B (3), two new natural products, penisochroman A (2) and 2,6-dihydroxy-4-[(2R)-2-hydroxyheptyl] benzoic acid (4), together with four known compounds (5-8) were isolated from wetland soil fungus Penicillium oxalicum GY1. All structures were elucidated by extensive NMR spectroscopic evidences together with mass spectrometry. The absolute configuration of penoxalin (1) was determined by calculated ECD spectrum, while the absolute configuration of new natural product penisochroman A (2) was established for the first time by single crystal X-ray diffraction. In addition, all compounds were evaluated for their cytotoxic activity in vitro. 2, 6-Dihydroxy-4-[(2R)-2-hydroxyheptyl] benzoic acid (4) displayed significant cytotoxicity against human esophageal carcinoma cells OE19 with an IC50 value of 5.50 µM.

TiO2 nanoparticles and C-Nanofibers modified magnetic Fe3O4 nanospheres (TiO2@Fe3O4@C-NF): A multifunctional hybrid material for magnetic solid-phase extraction of ibuprofen and photocatalytic degradation of drug molecules and azo dye.

Accurate sensitive analysis of drug ingredient substances in biological, pharmaceutical and environmental samples and removal of drug ingredient substances in environmental samples owngreat importance for sustaining viability. The realization of these processes using a single material offers significant advantages in terms of cost, time and ease of use. In this study, TiO2 nanoparticles and C-Nanofibers modified magnetic Fe3O4 nanospheres (TiO2@Fe3O4@C-NFs) synthesized as a multifunctional material employing a simple hydrothermal synthesis method. This innovative material was exploited in the magnetic solid-phase extraction (MSPE) method for the preconcentration of ibuprofen and photocatalytic degradation of antibiotics, non-steroidal anti-inflammatory drugs (NSAIDs), and azo dye. To our knowledge, no studies have been previously conducted using the same material as magnetic solid-phase extraction adsorbent and magnetically separable photocatalyst. The characterization of TiO2@Fe3O4@C-NFs was carried out by XRD, FE-SEM, EDX and Raman techniques. The main analytical parameters affecting MSPE performance of ibuprofen such as pH, sorbent amount eluent type and volume and sample volume were optimized. The optimum values of the method were determined at the following parameters: pH 4.0, adsorbent amount 150 mg and eluent 2 mL of acetone. Ibuprofen analysis after MSPE was carried out using a high-performance liquid chromatography diode array detection system (HPLC-DAD). The photocatalytic degradation efficiencies of TiO2@Fe3O4@C-NF hybrid material for probe-analytes reached 80-100% and the complete degradation attained within the range of 8-125 min under UV irradiation. Simple preparation, practical isolation from solutions, high efficiency, reproducibility, and sustainability are the main advantages of the TiO2@Fe3O4@C-NFs for MSPE and photocatalytic degradation applications.

Facile fabrication of Cu(II) coordinated chitosan-based magnetic material for effective adsorption of reactive brilliant red from aqueous solution.

In order to effectively remove reactive brilliant red (RBR) in aqueous solution, a novel Cu(II) coordinated chitosan-based magnetic composite (CTS-Cu@SiO2@Fe3O4) was prepared. The physicochemical properties of the resultant adsorbent were characterized by Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), vibrating sample magnetometer (VSM) thermogravimetric (TG) analysis, scanning electron microscopy (SEM) and N2 adsorption-desorption. The adsorption capacity toward RBR was systematically investigated as a function of contact time, solution pH, initial concentration, ionic strength and temperature. Compared with CTS@SiO2@Fe3O4, CTS-Cu@SiO2@Fe3O4 showed better adsorption performance in removing RBR, reaching a maximum of 880.84 mg/g at pH 4, which confirmed that the coordination of Cu(II) can improve the adsorption capability. The adsorption kinetics of CTS-Cu@SiO2@Fe3O4 was found to follow the pseudo-second-order kinetic model, and the equilibrium adsorption data were well described by the Freundlich isotherm model. Thermodynamic studies indicated that the adsorption process was spontaneous and endothermic. XPS analysis confirmed that the adsorption was mainly controlled by electrostatic interaction between copper/amino cation and RBR anion. Furthermore, regeneration experiments demonstrated that CTS-Cu@SiO2@Fe3O4 can be used repeatedly. In a word, CTS-Cu@SiO2@Fe3O4 can be served as a promising adsorbent for dye wastewater scavenging.

Biosorptive removal of acid orange 74 dye by HCl-pretreated Lemna sp.

Acid orange 74 (AO74) is a chromium-complex monoazo acid dye widely used in the textile industry. Due to being highly toxic and non-biodegradable, it must be removed from polluted water to protect the health of people and the environment. The aim of this study was two-fold: to evaluate the biosorption of AO74 from an aqueous solution by utilizing HCl-pretreated Lemna sp. (HPL), and to examine dye desorption from the plant material. The maximum capacity of AO74 biosorption (64.24 mg g-1) was reached after 4 h at the most adequate pH, which was 2. The biosorption capacity decreased 25% (to 48.18 mg g-1) during the second biosorption/desorption cycle and remained essentially unchanged during the third cycle. The pseudo-second-order kinetics model concurred well with the experimental results of assays involving various levels of pH in the eluent solution and distinct initial concentrations of AO74. NaOH (0.01 M) was the best eluent solution. The Toth isotherm model best described AO74 biosorption equilibrium data. FTIR analysis confirmed the crucial role of HPL proteins in AO74 biosorption. SEM-EDX and CLSM techniques verified the effective biosorption/desorption of the dye during the three cycles. Therefore, HPL has potential for the removal of AO74 dye from wastewaters.