Reactive Black Research Articles

Weakly-negatively-charged loose nanofiltration membranes tailored by polyethyleneimine for dye/salt separation

Loose nanofiltration membranes with a weakly negatively charged surface were made from interfacial polymerization between natural hydrophilic polymer carboxylated chitosan (C-CS) and trimesoyl chloride (TMC) firstly and further depositing branched polyethyleneimine (PEI) on top of the surface to tailor the membrane structures and surface charge properties. This kind of membrane was exploited for dye/salt separation in textile wastewater treatment. The effects of contents and molecular weights of PEI on the morphologies, surface charge, hydrophilicity, pore size, and dye/salt separation performance of the membrane were comprehensively investigated. We found that the top layer of PEI with a moderate molecular weight is suitable to form a loose structure for dye/salt separation. The optimized membrane has a comparable high water permeability (44.4 L/m2.h.bar), a low salt rejections (2.6 % for Na2SO4, 7.7 % for NaCl, and 6.8 % for MgCl2), a relatively high dye rejection (96.9 % for Congo Red, 85.4 % for Methyl Blue, 51.1 % for Bromophenol Blue, and 48.3 % for Reactive Black 5), and an extremely high CR/Na2SO4 fractionation ratio (37.27). Moreover, the resultant membrane shows excellent anti-fouling performance after 5 cycles (50 h) of filtration. It maintains a high Congo Red rejection during a 10-day long-term run. This study shows an easy way to fabricate and adjust the properties of loose nanofiltration membranes that work well for dye/salt separation using common and low-cost polymers. It shows promising potential in the application of textile wastewater treatment and resource recovery.

Effect of Beech Sawdust Conditions Modification on the Efficiency of the Sorption of Anionic and Cationic Dyes.

The article presents studies on the effect of the modification method of beech sawdust on the sorption capacity of the anionic dye Reactive Black 5 (RB5) as well as the cationic dye Basic Violet 10 (BV10). In the studies, the pH value, the dose of sawdust activated with epichlorohydrin and the dose of ammonia were determined for the efficiency of the removal of anionic and cationic dyes. In the next phase of the study, the pH and the dose of epichlorohydrin activator on the previously activated sorbent were determined. The modification proposed in the work, which consists in the amination of sawdust in direct reaction with ammonia, increased the efficiency of the sorption of anionic dyes. This reaction increased the positive charge on the surface of the sorbent by introducing -NH2 groups, which led to an increase in the electrostatic attraction between the sorbent and the anionic dye, but to a decrease in the interaction between the sorbent and the cationic dye.

A novel green approach for reactive printing of cotton/cellulosic regenerated blended fabrics using trisodium nitrilotriacetate

Owing to their comfort, handle, and aesthetic characteristics, cotton fabrics will always be the first and primary choice for clothing and apparel. In recent years, regenerated cellulosic fabrics like bamboo, Tencel, and modal fabrics have had many natural advantages. Fabrics based on blending cotton fibres with regenerated cellulosic fibres are considered promising products in textile industry sectors. Use of urea poses ecological problems associated with the high nitrogen content of the printing effluent. Therefore, urea reduction or elimination in reactive dye print pastes is of ecological interest. We report the use of trisodium nitrilotriacetate as a complete substitution of urea and alkali in the conventional reactive printing of cotton/cellulosic regenerated blended fabrics. CI Reactive Black 5 was selected for the present study. Three different print pastes containing urea/alkali, trisodium nitrilotriacetate/alkali and trisodium nitrilotriacetate without alkali were thoroughly investigated. Different factors that may affect the printability of cotton/cellulosic regenerated blended fabrics, such as the concentrations of dye, trisodium nitrilotriacetate, urea, absence or presence of alkali and steaming time in the prints obtained, were evaluated concerning colour strength, dye fixation, dye penetration, levelling, colure, and fastness properties. All printed fabrics using three print pastes obtained excellent to good fastness. The results proved the viability of using TNA as an environmentally friendly approach for urea/alkali-free printing of cellulosics with reactive dyes.

Hybrid composite beads of chitosan/graphene oxide for dye adsorption: characterizations, kinetic modeling and toxicity study

The current study aimed to the preparation of graphene oxide impregnated chitosan– polyvinyl alcohol hybrid beads (GO/CS-PVA) for the removal of Reactive Black 5 (RB5) dye from wastewater solutions, presenting them as a cost-effective alternative for wastewater treatment. These hybrid beads were fabricated using a dripping technique in an aqueous solution. The surface and structure of the material before and after adsorption process were studied by analyzing FTIR spectroscopy and Scanning electron microscope (SEM) as well as adsorption capacity was also evaluated. The results proved the successful synthesis of GO/CS-PVA beads and elucidated the physical adsorption mechanism of RB5. SEM images revealed uniform spherical beads with a rough surface, approximately 752 μm in diameter. Additionally, the evaluation of adsorption capacity showed that the optimum condition for RB5 adsorption is at pH = 3 while the kinetic investigations revealed that the adsorption process adhered to the pseudo-second-order model, indicating a chemisorption reaction. Furthermore, an increase in temperature from 25 to 65 °C enhanced the maximum adsorption capacity of GO/CS-PVA beads by 34%. The cytotoxic effect of the hybrid as measured on adipose derived stem cells via the MTT assay was negligible. In conclusion, it was proved that the eco-friendly GO/CS-PVA beads adsorbents can efficiently remove RB5 from wastewater in practical applications.

Comparative treatment of textile dye wastewater with chemical coagulants and bacterial exopolysaccharides

Traces of chemical coagulants, such as alum, commonly used in wastewater treatment, remain in the water effluent and also result in secondary sludge that is difficult to treat. On the other hand, Extracellular Polymeric Substances (EPS) are safer and can be used as alternative bio flocculants. A study was hence done to compare the effectiveness of the treatment of Reactive Black 5 (RB5) textile wastewater with chemical coagulants and bacterial EPS. The jar test method was used to treat the wastewater with Alum and Polyferrous Sulphate (PFS) at varied pH (2–10) and respective dose concentrations. EPS was produced by bacteria isolated from cotton gin trash soil collected from Kitui ginnery in Kenya. EPS treatment was done at 30 °C for 72 h. EPS-producing bacteria isolates were identified by molecular analysis. The chemically and EPS-treated wastewater was analyzed for color, Total Dissolved Solids (TDS), and Chemical Oxygen Demand (COD). Respective color and TDS removal capacity by PFS and alum were (86.1% and 42.18%) and (85.1% and 69%) at their optimal conditions of (pH 7 and 100 mg/L) and (pH 7 and 140 mg/L). Similarly, PFS and alum reduced COD by 27.25% and 26.65%. Respective dye removal by YEAK2 −5 and YEPD K2 −2 EPS was 69.1% and 85.7%. However, YEPD K2 −2 and YEAK2 −5 EPS caused a respective rise of TDS by 40.14% and 67.17%. The respective reduction of COD by YEPD K2 −2 and YEAK2 −5 EPS was 56.25% and 54.24%. The chemically and EPS-treated wastewater met the National Environment Management Authority (NEMA) limits. The YEPD K2 −2 and YEAK2 −5 isolates were both identified as Bacillus sp. GC–MS and FTIR analysis results indicated that the two EPS were heteropolysaccharides composed of different sugar derivatives and hydroxyl as the main functional group. The results for treatment of the dye wastewater by Alum, PFS, and EPS were therefore comparable. The bacterial EPS bio flocculants can therefore serve as effective and cleaner substitutes to the alum and PFS chemical coagulants.

Bio-Adsorbent for Elimination of Reactive Dye from Aqueous Solution: Kinetic and Statistical Modelling Study

Introduction/Background: The use of various dyes to colour products is a general practice in various industries. The occurrence of these dyes in water, even at small concentrations, is highly noticeable and aesthetically objectionable. In the present study, the applicability of inexpensive and eco-friendly bio-adsorbent has been tested as an alternative substitution of the commercially available activated carbon for the removal of reactive dye from the aqueous solution. Materials and Methods: Bio-adsorbent prepared from pomegranate peel was successfully used to remove the reactive dye (Reactive Black 5) from the aqueous solution. The effects of major parameters such as pH, adsorbent dosage, and contact time on dye removal efficiency were studied. Statistical models were articulated based on selected variables to optimize the decolourisation efficiency of the adsorption process using a full factorial central composite design. Results: Dye removal efficiency of close to 100% was observed at a pH 12 using 1 g adsorbent/ 200 mL dye solution within a contact time of 60 min., yielding a virtually colourless solution. A fixed-bed column study with an initial dye concentration of 100 mg/L at bed depths of 4 cm, 8 cm, and 12 cm yielded a breakthrough time of 300 min, 570 min, and 780 min, respectively. Discussion: Langmuir, Freundlich, and Temkin isotherm models were applied to analyze the sorption equilibrium parameters. The experimental results of the analysis revealed that the Langmuir isotherm fits better than the other isotherms with a linear regression coefficient (R2) of 0.99. The high correlation coefficient (R² > 0.95) and low p-values (< 0.0001) indicate that the model and its terms are significant, making it effective for optimizing operational parameters and accurately predicting the response. Conclusion: The breakthrough curve serves as a tool to evaluate the effectiveness of the prepared adsorbent in real-world applications. The present work not only provides an alternative to commercially available activated carbon for dye wastewater colour removal but also emphasizes the importance of repurposing fruit residues, which could otherwise become environmental pollutants if improperly disposed of.

Catalytic degradation of Reactive Black 5 through peroxymonosulfate activation with Co organic frameworks combined with graphite oxide

The development of high-efficiency catalysts for peroxymonosulfate (PMS) activation is critical for pollutant treatment in environmental applications. In this research, a Co organic framework (CoHHTP) combined with graphene oxide (GO) (CoHHTP/GO) with a 2D structure was prepared for PMS activation to treat the azo dye Reactive Black 5 (RBK5). The combination of CoHHTP and GO via oxygen groups resulted in the high activity of CoHHTP/GO, and almost 100 % performance was achieved within 30 min under various pH, temperature, PMS loading, and catalyst loading conditions. The maximum RBK5 removal efficiency was obtained with a catalyst loading of 3.0 g L−1, PMS loading of 0.5 mM, temperature of 25 °C, and pH of 6 with a pseudo-first-order kinetics k value of 0.1903 min−1. The activation energy of the CoHHTP/GO/PMS/RBK5 system was calculated to be 14.34 kJ mol−1. Meanwhile, radicals and nonradicals, including SO4·−, ·OH, ·O2−, and 1O2, were proven to be generated and involved in RBK5 degradation. Moreover, RBK5 degradation pathways were identified through experimental research and density functional theory calculation.

Kinetics of the decomposition of reactive black 5 on carbon nanostructured adsorbents

Textile industry effluents, containing vast quantities of toxic organic pollutants and synthetic dyes like Reactive Black 5 (RB5), pose a significant environmental threat. RB5 contamination can harm ecosystems and human health, necessitating effective treatment for water recycling and compliance with quality standards. Traditional methods like filtration often fall short in removing dye chemicals. This study examines the efficiency of nanocarbon-based adsorbents in removing RB5 from textile industry effluents. RB5 solutions at concentrations of 10 µM, 30 µM, 60 µM and 100 µM were investigated and characterized using scanning electron microscopy (SEM) and UV-Vis spectrophotometry. Activated carbon (AC) demonstrated the highest degree of RB5 decomposition, outperforming graphene nanoplatelets (GNPs) and graphene oxide (GO) and offering a promising solution for mitigating textile wastewater pollution. Kinetic studies revealed that RB5 adsorption follows a pseudo-second-order model for all adsorbents. The rate constants were determined using PSO kinetics and they were comparable with the rate constants of prior studies, indicating the applicability of the model to the study of the kinetics of similar dye adsorption and decomposition processes.

Micro-nano bubbles in action: AC/TiO2 hybrid photocatalysts for efficient organic pollutant degradation and antibacterial activity

Developing highly active and sustainable photocatalysts is crucial for environmental remediation. This work focuses on the enhanced photocatalytic degradation efficiency of synthetic dyes using TiO2-coated AC hybrid photocatalysts under MNB aeration. The TiO2-coated AC hybrid photocatalyst (HP) was synthesized via a sol-gel method and characterized using XRD, FTIR, SEM, EDS, HR-TEM, and DRS. The study investigated the photocatalytic degradation of three dyes indigo carmine (IC), reactive black 5 (RB5), and methylene blue (MB) in wastewater, with initial dye concentrations ranging from 10 to 100 μM. Under UVA irradiation, the hybrid photocatalyst with MNB aeration (HP + UVA + MNB) achieved the highest degradation efficiencies of 69.09%, 60.06%, and 55.19% for IC, MB, and RB5, respectively. Further analysis showed that the chromophores and complex structures of these dyes were broken into intermediate products. The Langmuir-Hinshelwood kinetic model was used to describe the reaction mechanisms. The HP + UVA + MNB system demonstrated superior photocatalytic degradation activity, making it suitable for operational and environmental applications in dye wastewater treatment. Additionally, the antibacterial properties of AC and HP were tested at 100 μg/mL, showing effectiveness against both Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli.

Photodegradation of RB5 dye with modified zeolites: influence of temperature and UV irradiation

Abstract This study explores the photocatalytic degradation of Reactive Black 5 (RB5) dye using thermally modified natural zeolites, aiming to improve water purification methods. Zeolites were calcined at 250 °C, 350 °C, and 500 °C, and characterized through x–ray diffraction (XRD), Scanning Electron Microscopy (SEM), and Fourier Transform Infrared Spectroscopy (FTIR) to analyze their structural and morphological transformations. The results reveal that calcination significantly enhances the photocatalytic performance, particularly for ZNM500, which exhibited the highest efficiency, reaching a 60% removal rate of RB5. The degradation process follows a pseudo-first-order kinetic model at lower dye concentrations but adheres more closely to the Langmuir–Hinshelwood equation at higher concentrations, emphasizing the role of surface adsorption in catalysis. UV irradiation was a key factor in boosting reaction rates, with shorter wavelengths (254 nm) providing greater energy, leading to more effective dye breakdown by facilitating the generation of reactive hydroxyl radicals (·OH). These findings suggest that thermally modified zeolites, especially ZNM500, represent a promising solution for wastewater treatment, offering an efficient, cost–effective, and environmentally friendly approach to removing synthetic dyes from contaminated water sources.

Preparation of Mn-Ce oxide-loaded Al2O3 by citric acid-assisted impregnation for enhanced catalytic ozonation degradation of dye wastewater

The performance of supported catalysts is significantly affected by the dispersion degree of the active components on the support. In this study, citric acid (CA) was used as a modifier to prepare Al2O3 supported Mn-Ce oxides (Mn-Ce/CA-Al2O3) by the impregnation-calcination method. The characterization results showed that adding citric acid enhanced the dispersion of Mn-Ce oxides on the support, rendering Mn-Ce/CA-Al2O3 with a larger specific surface area and abundant surface hydroxyl groups, thereby providing more reaction sites for catalytic ozonation. The Mn-Ce/CA-Al2O3 exhibited excellent catalytic ozonation performance in degrading Reactive Black 5 (RB5) dye. It achieved nearly complete decolorization of RB5 within 60 min, with a COD removal efficiency of 60%, which was superior to the sole ozonation (30%). Furthermore, the Mn-Ce/CA-Al2O3 system demonstrated significant degradation of RB5 over a wide pH range of 3 to 11. Based on the XPS and EPR analysis results, a preliminary mechanism of catalytic ozonation over the Mn-Ce/CA-Al2O3 was proposed. The redox cycle of Mn3+/Mn4+ and Ce3+/Ce4+ effectively accelerated the electron transfer process, thus promoting the generation of reactive oxygen species (ROS) and improving the degradation of RB5. Meanwhile, the Mn-Ce/CA-Al2O3 exhibited superior catalytic stability and effective treatment capabilities for real dye wastewater.

The Wood-rot Basidiomycete Candolleomyces eurysporus VAST02.52 Produces a Versatile Peroxidase that Catalyses the Biotransformation of α-Pinene to Release Verbenone

Background Versatile peroxidase (VP; EC 1.11.1.16) has recently emerged as a novel peroxidase highly valued in biotechnology due to its exceptional ability to oxidize a diverse range of substrates into value-added products. Objectives To gain insight into the versatile peroxidase system from fungi, this study was designed to purify and characterize a CeuVP from the newly isolated fungus Candolleomyces eurysporus and to investigate its involvement in the biotransformation of plant α-pinene. Materials and methods The fungal isolate was identified by analysis of the internal transcribed spacer region. VP-active protein was purified from liquid culture of C. eurysporus VAST02.52 by using fast protein liquid chromatography. The catalytic properties and stability of enzyme were studied for various substrates, different pH- and temperatures. Moreover, its involvement in the biotransformation of plant α-pinene was assessed by HPLC chromatography. Results CeuVP was successfully purified with 27.3-fold purity and a 20.9% yield by using three steps of anion exchange and size exclusion chromatography. The molecular weight of CeuVP was determined to be 40 kDa by SDS-PAGE electrophoresis. This pure enzyme exhibited optimal activity at pH 4.0 and 35 °C. CeuVP showed the highest specific activity of 231.6 U/mg against ABTS, followed by Mn2+ (205.8 U/mg), veratryl alcohol (112.7 U/mg), cathecol (77.8 U/mg), p-aminophenol (68.9 U/mg), RBBR (56.2 U/mg), 4-methoxyphenol (31.1 U/mg), guaiacol (18.3 U/mg), and Reactive Black 5 (12.9 U/mg). Moreover, CeuVP catalyzed the oxidation of α-pinene derived from the essential oil of Eucalyptus robusta to release verbenone as the sole metabolite after a 7 h incubation. Conclusions Versatile peroxidase ( CeuVP) from C. eurysporus VAST02.52 exhibits the highest specific activity against ABTS while also catalyzing oxidation of various substrates tested. Moreover, this study indicated that CeuVP could be effective in the bioconversion of α-pinene into verbenone, a promising compound with numerous applications in the flavors and fragrances industry.

Modification of polysulfone membranes using magnetite nanoparticles containing sulfonic acid and heteropoly acid groups to improve permeability and antifouling properties

To increase the performance of ultrafiltration membranes, it is necessary to develop new materials. In this study, membrane production was carried out using magnetite nanoparticles functionalized by sulfonic acid and phosphotungstic acid (HPW) to increase permeability and improve antifouling properties. Firstly, Fe3O4@SiO2@NH2-SO3H (FSNS) and Fe3O4@SiO2@NH2-SO3H-HPW (FSNSPW) materials were synthesized. Then, different amounts of the nanoparticles were added to the membrane solutions. While the pure water flux was 164.2 LMH in the bare membranes, it was observed as 202.8 LMH and 195 LMH as a result of adding 0.5 % FSNSPW and FSNS. While Pb removal efficiency was 90 % in the bare membrane, it was measured as 97 % for 0.1 % FSNSPW and 89.6 % for 0.5 % FSNS. Maximum flux recovery ratio is 65.3 % for 0.5 % FSNSPW and 63.4 % for 1 % FSNS. Additionally, the highest Reactive Red 120 dye permeation flux was 72.2 LMH for 0.1 % FSNSPW and 71.9 LMH for 0.1 % FSNS membrane. Additionally, the highest permeation flux of Reactive Black 5 dye solution is 83.3 LMH for 0.5 % FSNSPW and 95 LMH for 0.5 % FSNS membrane. It could be concluded that the presence of the HPW group can improve the performance of the membranes.

THE COMBINATION OF WASTE PRODUCTS FROM CHITIN AND SAWDUST TO REMOVE ANIONIC AND CATIONIC DYES

The application of the immobilisation method – which consists of immobilising modified sawdust in a carrier, a chitosan gel – enabled the development of a new sorbent. By combining waste products from chitin and sawdust, the properties of both adsorbents were utilised. This paper evaluated the adsorption efficiency of four dyes – Reactive Yellow 84, Reactive Black 8, Basic Violet 10 and Basic Green 4 – on four adsorbents – chitin flakes, chitosan flakes, chitosan beads and sawdust immobilised in chitosan beads. The latter adsorbent showed good adsorption properties for both anionic and cationic dyes. The experimental results showed a relationship between the amount of adsorbed and desorbed dye and the type of adsorbent. Chitin flakes showed the lowest adsorption capacity, regardless of the type of dye. The immobilisation of modified sawdust in chitosan had a particularly positive effect on the binding efficiency of cationic dyes.

Dual Eu3+ and Er3+ doping in ZnO nanoporous 2D frameworks for tuning photocatalytic activity, linear and non-linear optical response

Recent days, the greater attention of research materials are focusing on the porous nano frame structure due to their distinctive properties and high photocatalytic activity. The porous defective materials revealed a significant role in numerous research fields like sensors, catalysts, energy production, magnetic memory storage, bio medical etc. In our work, pure ZnO and 4f shell shielded rare earth metals doped ZnO metal oxide nanomaterials attributed in the photocatalytic dye degradation, non-linear optical and magnetic properties. We were synthesized pure ZnO and ZnO0.1–2xEuxErxHMT0.1–2x (2x = 0.025,0.05,0.075, 0.010 wt%) nanoparticles using a straightforward hydrothermal route. The hexagonal wurtzite structure of ZnO and Eu:Er-doped ZnO (Eu:Er@ZnO) exhibited by PXRD, and the optical bandgap (Eg) range from 3.14 eV to 3.18 eV was determined by Tauc relation (αhγ)2 = 0. The porous nanoplate morphology of as-synthesized materials revealed by HR-SEM and HR-TEM techniques. All synthesized materials exposed weak ferromagnetic property nature by VSM studies. Among all the synthesized materials, the 0.0025 wt% Eu:Er@ZnO nanoparticles exhibited porous nanoplate structures capable of catalyzing the breakdown of reactive black 5 (RB5) dye, achieving a photocatalytic activity of 93.2 % after 65 min of UV light exposure. The dopant concentration significantly influenced this photocatalytic activity, with lower concentrations showing enhanced performance, particularly in acidic conditions. Moreover, all synthesized porous nano-plate materials followed pseudo-first-order kinetics. Additionally, the Z-scan technique was employed to assess the nonlinear optical properties of the synthesized materials using Q-switched nanosecond Nd laser pulses at 532 nm wavelength. The open-aperture Z-scan revealed reverse saturable absorption (RSA) in all samples. The Eu:Er@ZnO porous nano-plates exhibited promising nonlinear absorption characteristics, with a higher nonlinear absorption coefficient ranging from 5.21 to 7.84 × 10−11 m/W and a lower optical limiting threshold between 0.87 and 0.95 × 1012 W/m2.

Macadamia nut residue-derived biochar: An eco-friendly solution for β-naphthol and Reactive Black-5 removal

The generation of liquid waste containing dyes and complex organic compounds is a problem in the textile industries. In this work, we evaluated the use of macadamia nut residue as a precursor of a biochar for the treatment of these effluents through the adsorption process. The macadamia nut endocarp undergoes a sequential treatment involving pyrolysis at 600 °C followed by physical activation with CO2 and H2O vapor at 700 °C. Characterization of the resulting macadamia nut residue-derived biochar (MB) is accomplished through various techniques, including X-ray diffractometry (XRD), thermogravimetric analysis (TGA), scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM-EDS), nitrogen physisorption analysis and the pH at the zero charge point (pHZCP). Performance studies reveal that pH exerts minimal influence on the adsorption phenomenon. The Elovich kinetic model effectively describes the adsorption kinetics for both β-naphthol and Reactive Black 5 (RB5), with adjusted coefficients of determination (R2adj) of 0.99 and 0.94, respectively. Further analysis using the intraparticle diffusion model demonstrates that β-naphthol adsorption kinetics involve multiple mechanisms, while RB5 adsorption is predominantly governed by intraparticle diffusion. Equilibrium adsorption data for both adsorbates fit well with the Sips isothermal model, yielding maximum adsorption capacities of qmax β-naphthol = 15.16 mg∙g−1 and qmax RB5 = 3.08 mg∙g−1 at 55 °C. The adsorption process for both compounds is spontaneous and endothermic, based on the enthalpy values, it can be inferred that the β-naphthol adsorption is governed by weak van der Waals forces, indicating physisorption. As for RB5, the enthalpy value suggests that the phenomenon occurs due to electrostatic interactions between the molecule and the surface groups with higher energy involved. This study highlights the potential of macadamia nut residue biomass as a precursor for biochar, demonstrating its favorable attributes for application as an effective adsorbent material in the removal of organic compounds such as β-naphthol and RB5 from wastewater streams within the textile industry.

A Facile and Rapid Immobilization Method of Titanium Dioxide-Alginate Composite for The Photocatalytic Removal of Reactive Black-5

A facile and rapid approach to immobilize nano-sized titanium dioxide (TiO2) using a renewable biopolymer (i.e. alginate) has been successfully demonstrated. TiO2 exhibits a positively charged surface in acidic environment due to the presence of hydroxyl groups. Meanwhile, alginate polymer is negatively charged at any pH due to the presence of carboxylic group in the polymer chain. The negatively charged alginate polymer and positively charged TiO2 formed composite instantaneously when the alginate polymer was introduced into the TiO2 nanoparticles suspension. The TiO2-alginate (TiO2-A) composite photocatalyst was characterized using thermogravimetric analysis (TGA), field emission-scanning electron microscopy (FE-SEM) coupled with energy dispersive X-ray (EDX) analysis and Fourier Transform Infrared (FTIR). Thermogravimetric analysis indicated that incorporating TiO2 into sodium alginate increases its decomposition temperature due to the stability of TiO2 at elevated temperatures, with the TiO2 content estimated in the composite being 55.6%, lower than the theoretical calculation of 62.8%. FTIR analysis revealed a shift in the peak of the carboxylic group of sodium alginate, suggesting composite formation through electrostatic interactions with TiO2 nanoparticles, while FESEM analysis showed that the TiO2-A composite surface exhibited more pores compared to protonated alginate. The TiO2-A composite was able to remove 90% of the Reactive Black 5 (RB5) in less than 200 min under Ultra-violet (UV) illumination. The optimal pH to remove RB5 was found to be pH 2 due strong electrostatic attraction of negatively charged RB5 on the positive surface of TiO2 nanoparticles. The photocatalyst can be recovered by simple separation method, i.e. gravitational settling, and reused for 10 consecutive cycles with efficiency greater than 90% consistently. The TiO2-A composite is a promising immobilized photocatalyst for practical application in wastewater treatment. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Recent Advances in Utilizing Lignocellulosic Biomass Materials as Adsorbents for Textile Dye Removal: A Comprehensive Review.

This review embarks on a comprehensive journey, exploring the application of lignocellulosic biomass materials as highly effective adsorbents for the removal of textile dyes (cationic and anionic dyes) from wastewater. A literature review and analysis were conducted to identify existing gaps in previous research on the use of lignocellulosic biomass for dye removal. This study investigates the factors and challenges associated with dye removal methods and signifies their uses. The study delves into the pivotal role of several parameters influencing adsorption, such as contact time, pH, concentration, and temperature. It then critically examines the adsorption isotherms, unveiling the equilibrium relationship between adsorbent and dye and shedding light on the mechanisms of their interaction. The adsorption process kinetics are thoroughly investigated, and a detailed examination of the adsorbed rate of dye molecules onto lignocellulosic biomass materials is carried out. This includes a lively discussion of the pseudo-first, pseudo-second, and intra-particle diffusion models. The thermodynamic aspects of the adsorption process are also addressed, elucidating the feasibility and spontaneity of the removal process under various temperature conditions. The paper then dives into desorption studies, providing insights into the regeneration potential of lignocellulosic biomass materials for sustainable reusability. The environmental impact and cost-effectiveness of employing lignocellulosic biomass materials in textiles including Congo Red, Reactive Black 5, Direct Yellow 12, Crystal Violet, Malachite Green, Acid Yellow 99, and others dyes from wastewater treatment are discussed, emphasizing the significance of eco-friendly solutions. In summary, this review brings together a wealth of diverse studies and findings to present a comprehensive overview of lignocellulosic biomass materials as adsorbents for textile cationic and anionic dye removal, encompassing various aspects from influential parameters to kinetics, adsorption isotherms, desorption, and thermodynamics studies. Its scope and other considerations are also discussed along with its benefits. The collective knowledge synthesized in this paper is intended to contribute to the advancement of sustainable and efficient water treatment technologies in the textile industry.

High adsorption capacities for dyes by a pH-responsive sodium alginate/sodium lignosulfonate/carboxylated chitosan/polyethyleneimine adsorbent

Dyes are indispensable for the rapid development of society, but untreated dye wastewater can threaten human health. In this study, an adsorbent (SA/SL/CCS/PEI@MNPs) was synthesized by one-pot method using magnetic nanoparticles (MNPs), sodium alginate (SA), sodium lignosulfonate (SL), carboxylated chitosan (CCS) and polyethyleneimine (PEI). The adsorbent was mesoporous micrometer-sized particles with pore size of 34.92 nm, which was favorable for dynamic column experiments. SA/SL/CCS/PEI@MNPs possessed pH-responsive performance. Under acidic condition, the maximum adsorption capacities for anionic dyes (tartrazine, reactive black-5, indigo carmine) reached >550 mg/g. Under alkaline condition, those for cationic dyes (methylene blue, methyl violet, neutral red) exceeded 1900 mg/g. The function of the various modifiers was investigated. The results indicated that the incorporation of SL, CCS and PEI was able to provide plenty of sulfonate, carboxylate and amino/imine reactive groups so that adsorption capacities of dyes were improved. The adsorption mechanism was explored by FTIR and XPS. At the same time, the adsorption mechanism was more deeply analyzed using molecular dynamics simulations and radial distribution function. It was demonstrated that the dyes adsorption on the SA/SL/CCS/PEI@MNPs was mainly due to electrostatic attraction and π-π interaction. In addition, the adsorbent had good reusability, and the removal still reached over 90 % after five cycles. In conclusion, the adsorbent displayed a broad prospect for the adsorption of organic dyes.

Heterologous expression and characterization of a dye-decolorizing peroxidase from Ganoderma lucidum, and its application in decolorization and detoxifization of different types of dyes.

Dye-decolorizing peroxidases (DyPs) belong to a novel superfamily of heme peroxidases that can oxidize recalcitrant compounds. In the current study, the GlDyP2 gene from Ganoderma lucidum was heterologously expressed in Escherichia coli, and the enzymatic properties of the recombinant GlDyP2 protein were investigated. The GlDyP2 protein could oxidize not only the typical peroxidase substrate ABTS but also two lignin substrates, namely guaiacol and 2,6-dimethoxy phenol (DMP). For the ABTS substrate, the optimum pH and temperature of GlDyP2 were 4.0 and 35°C, respectively. The pH stability and thermal stability of GlDyP2 were also measured; the results showed that GlDyP2 could function normally in the acidic environment, with a T50 value of 51°C. Moreover, compared to untreated controls, the activity of GlDyP2 was inhibited by 1.60 mM of Mg2+, Ni2+, Mn2+, and ethanol; 0.16 mM of Cu2+, Zn2+, methanol, isopropyl alcohol, and Na2EDTA·2H2O; and 0.016 mM of Fe2+ and SDS. The kinetic constants of recombinant GlDyP2 for oxidizing ABTS, Reactive Blue 19, guaiacol, and DMP were determined; the results showed that the recombination GlDyP2 exhibited the strongest affinity and the most remarkable catalytic efficiency towards guaiacol in the selected substrates. GlDyP2 also exhibited decolorization and detoxification capabilities towards several dyes, including Reactive Blue 19, Reactive Brilliant Blue X-BR, Reactive Black 5, Methyl Orange, Trypan Blue, and Malachite Green. In conclusion, GlDyP2 has good application potential for treating dye wastewater.