pH-triggered polydopamine-decorated nanocellulose membranes for continuously selective separation of organic dyes.

Membrane separation technology has emerged as a powerful tool to separate organic dyes from industrial wastewater. However, continuously selective separation of organic dyes with similar molecular weight remains challenging. Herein, we presented a pH-triggered membrane composed of polydopamine-decorated tunicate-derived cellulose nanofibers (PDA@TCNFs) for selective separation of organic dyes. Such self-supporting membranes with nanoporous structure were fabricated by facile vacuum-assisted filtration of PDA@TCNF suspension. The incorporation of polydopamine not only enhanced the stability of the membranes, but also endowed membranes with excellent pH sensitivity, facilitating the continuously selective separation of organic dyes. These pH-triggered PDA@TCNF membranes could selectively separate Methyl Orange (MO) and Rhodamine B (RB) from the MO/RB mixed solution by switching the pH values. The continuously selective separation of the MO/RB mixed solution was demonstrated, where both MO and RB recovery ratios maintained at ∼99 % during 50 repeated cycles. This work provides a new strategy to develop a pH-triggered sustainable nanocellulose-based membrane for continuously selective separation of mixed dyes.

A novel sponge composite of chitosan-sodium tripolyphosphate-melamine for anionic dye Orange II removal.

Since the potential carcinogenic, toxic and non-degradable dyes trigger serious environmental contamination by improper treatment, developing novel adsorbents remains a major challenge. A novel high efficiency and biopolymer-based environmental-friendly adsorbent, chitosan­sodium tripolyphosphate-melamine sponge (CTS-STPP-MS) composite, was prepared for Orange II removing with chitosan as raw material, sodium tripolyphosphate as cross-linking agent. The composite was carefully characterized by SEM, EDS, FT-IR and XPS. The influence of crosslinking conditions, dosage, pH, initial concentration, contacting time and temperature on adsorption were tested through batch adsorption experiments. CTS-STPP-MS adsorption process was exothermic, spontaneous and agreed with Sips isotherm model accompanying the maximum adsorption capacity as 948 mg∙g-1 (pH = 3). Notably, the adsorption performance was outstanding for high concentration solutions, with a removal rate of 97 % in up to 2000 mg∙L-1 OII solution (100 mg sorbent dosage, 50 mL OII solution, pH = 3, 289.15 K). In addition, the adsorption efficiency yet remained 97.85 % after 5 repeated adsorption-desorption cycles. The driving force of adsorption was attributed to electrostatic attraction and hydrogen bonds which was proved by adsorption results coupled with XPS. Owing to the excellent properties of high-effective, environmental-friendly, easy to separate and regenerable, CTS-STPP-MS composite turned out to be a promising adsorbent in contamination treatment.

An eco-friendly chitosan-genipin/SiO2 composite for reactive orange 16 dye removal: Insights into adsorption statistical modeling and mechanism.

The present work develops an effective bioadsorbent of cross-linked chitosan-genipin/SiO2 adsorbent (CHI-GNP/SiO2). The developed CHI-GNP/SiO2 was employed for the removal of organic dye (reactive orange 16, RO16) from simulated wastewater. The optimization of the fundamental adsorption variables (CHI-GNP/SiO2 dose, time, and pH) via the Box-Behnken design (BBD) was attained for achieving maximal adsorption capacity and high removal efficiency. The good agreement between the Freundlich isotherms and empirical data of RO16 adsorption by CHI-GNP/SiO2 indicates that the adsorption process follows a multilayer adsorption mechanism. The reasonable agreement between the pseudo-second-order model and the kinetic data of RO16 adsorption by CHI-GNP/SiO2 was obtained. The maximum RO16 adsorption capacity (qmax) of CHI-GNP/SiO2 was identified to be 57.1 mg/g. The adsorption capacity of CHI-GNP/SiO2 is attributed to its unique surface properties, including its highly porous structure and the presence of functional groups such as amino and hydroxyl groups. According to the results of this investigation, CHI-GNP/SiO2 has the potential to be an adsorbent for the removal of acidic dyes from wastewater.

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.

Melamine sponges incorporated azo-linked porous organic polymer as adsorbent for extraction and determination of six B vitamins using pipette tip micro solid-phase extraction.

A novel azo-linked porous organic polymer (AL-POP) was synthesized from caffeic acid and benzidine via an azo-coupling reaction and characterized by FTIR, SEM-EDS, BET, TGA, XRD and zeta potential analysis. AL-POPs were incorporated into melamine sponges and used for pipette tip micro solid-phase extraction (PT-MSPE) of six types of B vitamins (including thiamine, riboflavin, nicotinamide, pyridoxine, folic acid, and cyanocobalamin). After extraction, the samples were analyzed using high performance liquid chromatography-diode array detection (HPLC-DAD) system. The effect of AL-POP composition on the extraction efficiency (EE) of vitamins was investigated and benzidine to caffeic acid mol ratio of 1.5, 3.35 mmol of NaNO2, and reaction time of 8 h were selected as optimum conditions. The efficiency of the extraction process was improved by optimizing various parameters such as the amount of sorbent, pH and ionic strength of the sample, sample volume, number of sorption and desorption cycles, type of wash solvent, and type and volume of eluent solvent. Linearity (R2≥0.9987), Limit of detection (LOD) (11.88-18.97 ng/mL), limit of quantification (LOQ) (39.62-63.23 ng/mL), and enrichment factor (EF) (1.27-4.31) were obtained using calibration curves plotted under optimum conditions. Recovery values of these six B vitamins in the spiked multivitamin syrup samples varied from 80.01% to 108.35%, with a relative standard deviation (RSD) below 5.44%. Eventually, the optimized method was successfully used to extract and quantify the B vitamins in multivitamin syrup and non-alcoholic beer.

Facile synthesis of amino-modified magnetic covalent organic framework for the efficient extraction and determination of anionic azo dyes in carbonated beverages.

In this work, a novel magnetic covalent organic framework (COF (TpPa-NH2) @ Fe3O4) was prepared via two step by simple solvent method for the extraction of anionic azo dye residues in food. The as-prepared COF (TpPa-NH2) @ Fe3O4 nanocomposite was characterised by scanning electron microscope, transmission electron microscope, Fourier transform-infrared spectroscopy, X-ray diffraction and vibrating sample magnetometer. Before high-performance liquid chromatography with ultraviolet detection (HPLC-UV) determination, it was used as magnetic adsorbent for magnetic solid-phase extraction (MSPE) to extract and pre-concentrate three anionic azo dyes in carbonated beverage samples. The several key extraction and desorption parameters affecting the extraction recovery rate were investigated, including extraction time, pH of the solution, amount of material, adsorption time, elution solvent, pH of elution solvent, type of elution solvent, elution volume and elution time. Under optimised conditions, this method has good linearity between 5 and 500 µg L-1 (correlation coefficient > 0.9986). The limit of detection was 2.3-3.4 µg L-1. The recoveries of the samples were between 87.5 and 96.9%, and the relative standard deviation lower than 4.6%. The developed method has broad application prospects for the analysis of anionic azo dyes in carbonated beverages.

Photocatalytic degradation of Acid Red 18 by synthesized AgCoFe2O4@Ch/AC: Recyclable, environmentally friendly, chemically stable, and cost-effective magnetic nano hybrid catalyst.

Chitosan (Ch) is a linear biodegradable natural carbohydrate polymer and the most appealing biopolymer, such as low-cost biodegradability, biocompatibility, hydrophilicity, and non-toxicity. In this case, Ch was utilized to synthesize AgCoFe2O4@Ch/Activated Carbon (AC) by the modified microwave-assisted co-precipitation method. The physical and chemical structure of magnetic nanocomposites was analyzed and characterized by Field Emission Scanning Electron Microscope (FESEM), Transmission electron microscopy (TEM), X-ray diffraction (XRD), Energy Dispersive Spectroscopy (EDS), Diffuse Reflection Spectroscopy (DRS), Value stream mapping (VSM), Fourier transform spectroscopy (FTIR) and BET. The effects of various parameters on the removal of dye (Acid Red18), including catalyst dose, dye concentration, pH, and time were studied. Results showed that the highest removal efficiencies were 96.68 % and 84 % for the synthetic sample and actual wastewater, respectively, in optimal conditions (pH: 3, the initial dye concentration: 10 mgL-1, the catalyst dose: 0.14 gL-1, time: 50 min). Mineralization, according to the COD analysis, was 89.56 %. Photocatalytic degradation kinetics of Acid Red 18 followed pseudo-first order and Langmuir-Hinshelwood with constants of kc = 0.12 mg L-1 min-1 and KL-H = 0.115 Lmg-1. Synthesized photocatalytic AgCoFe2O4@Ch/AC showed high stability and after five recycling cycles was able to remove the pollutant with an efficiency of 85.6 %. So, the synthesized heterogenous magnetic nanocatalyst AgCoFe2O4@Ch/AC was easily recycled from aqueous solutions and it can be used in the removal of dyes from industries with high efficiency.

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.