High capacity and selective adsorption of Congo red by cellulose-based aerogel with mesoporous structure: Adsorption properties and statistical data simulation.

Large quantities of organic dyes are discharged into the environment, causing serious damage to the ecosystem. Therefore, it is urgent to develop inexpensive adsorbents to remove organic dyes. A novel cellulose-based aerogel (MPPA) with 3D porous structure was prepared by using cassava residue (cellulose) as basic construction blocks, doping ferroferric oxide (Fe3O4) for magnetic separation, and applying polyethyleneimine (PEI) as functional material for highly efficient and selective capture of Congo red (CR). MPPA exhibited porous network structure, numerous active capture sites, nontoxicity, high hydrophilicity, and excellent thermal stability. MPPA showed superior adsorption property for CR, with an equilibrium adsorption capacity of 2018.14 mg/g, and still had an adsorption property of 1189.31 mg/g after five recycling procedures. In addition, MPPA has excellent selectivity for CR in four binary dye systems. The adsorption behavior of MPPA on CR was further explored using a multilayer adsorption model, EDR-IDR hybrid model and AOAS model. Electrostatic potential and independent gradient models were used to further verify the possible interaction between MPPA and CR molecules. In conclusion, MPPA is a promising adsorbent in the field of treating anionic dyes.

High-efficient removal of anionic dye from aqueous solution using metal-organic frameworks@chitosan aerogel rich in benzene structure.

With the exponentially increase of dye pollutants, the purification of dye wastewater has been an urgent ecological problem. As a novel type of porous adsorbent, metal-organic frameworks still face challenges in recyclability, agglomeration, and environmentally unfriendly synthesis. Herein, MOF-525 was in-situ growth onto the surface of the chitosan (CS) beads to fabricate MOF-525@CS aerogel. CS was utilized as substrate to uniformly disperse MOF-525, thereby significantly mitigating agglomeration and improving recyclability of MOF-525. The characterization results shown that MOF-525@CS aerogel had a high specific surface area of 103.0 m2·g-1, and MOF-525 was uniformly distributed in the 3D porous structure of CS, and the presence of benzoic acid was detected. The MOF-525@CS aerogel had a remarkable adsorption capacity of 1947 mg·g-1 for Congo red, which is greater than the sum of its parts. MOF-525@CS aerogel also inherited the rapid adsorption ability of MOF-525, removing 80 % of Congo red within 600 min. Such excellent adsorption performance can be attributed to the benzoic acid trapped by CS via CN band to enhance the π-π stacking interactions. Additionally, the utilization of benzoic acid makes the synthesis process of MOF-525@CS aerogel more environmentally friendly. The high-efficient MOF-525@CS aerogel is a competitive candidate for dye pollution adsorption.

Bacterial cellulose microfiber reinforced hollow chitosan beads decorated with cross-linked melamine plates for the removal of the Congo red.

In this epoch, the disposal of multipollutant wastewater inevitably compromises life on Earth. In this study, the inclusion of Bacterial cellulose microfilaments reinforced chitosan adorned with melamine 2D plates creates a unique 3D bead structure for anionic dye removal. The establishment of an imine network between melamine and chitosan, along with the quantity of inter- and intra­hydrogen bonds, boosts the specific surface area to 106.68 m2.g-1. Removal efficiency and in-depth comprehension of synthesized adsorbent characteristics were assessed using batch adsorption experiments and characterization methods. Additionally, pH, adsorbent quantity, time, beginning concentration of solution, and temperature were analyzed and optimized as adsorption essential factors. Owing to the profusion of hydroxyl, amine, imine functional groups and aromatic rings, the synthesized adsorbent intimated an astonishing maximum adsorption capacity of 3168 mg.g-1 in Congo red dye removal at pH 5.5. Based on the kinetic evaluation, pseudo-second-order (R2 = 0.999), pseudo-first-order (R2 = 0.964), and Avrami (R2 = 0.986) models were well-fitted with the kinetic results among the seven investigated models. The isothermal study reveals that the adsorption mechanism predominantly follows the Redlich-Peterson (R2 = 0.996), Koble-Carrigan, and Hill isotherm models (R2 = 0.994). The developed semi-natural sorbent suggests high adsorption capacity, which results from its exceptional structure, presenting promising implications for wastewater treatment.

Anakinra-Associated Systemic Amyloidosis.

OBJECTIVE: To describe a 41-year-old woman with a history of neonatal onset multisystem inflammatory disease, on treatment with daily subcutaneous injections of 600 mg of recombinant interleukin-1 receptor antagonist (IL-1Ra) protein, anakinra, since the age of 28, who presented with golf-ball size nodules at the anakinra injection sites, early satiety, new onset nephrotic syndrome in the context of normal markers of systemic inflammation. METHODS: Clinical history and histologic evaluation of biopsies of skin, gastric mucosa, and kidney with Congo-red staining and proteomic evaluation of microdissected Congo red-positive amyloid deposits by liquid chromatography-tandem mass spectrometry. RESULTS: The skin, stomach, and kidney biopsies all showed the presence of Congo red-positive amyloid deposits. Mass spectrometry-based proteomics demonstrated that the amyloid deposits in all sites were of AIL1RAP (IL-1Ra protein)-type. These were characterized by high spectral counts of the amyloid signature proteins (apolipoprotein AIV, apolipoprotein E, and serum amyloid P-component) and the amyloidogenic IL-1Ra protein, which were present in Congo red-positive areas and absent in Congo red-negative areas. The amino acid sequence identified by mass spectrometry confirmed that the amyloid precursor protein was recombinant IL-1Ra (anakinra) and not endogenous wild-type IL-1Ra. CONCLUSION: This is the first report of iatrogenic systemic amyloidosis due to an injectable protein drug, which was caused by recombinant IL1Ra (anakinra).

Nanostructural Design of ZnO Using an Agro-Waste Extract for a Sustainable Process and Its Photocatalytic Activity.

The use of agro-waste extracts (AWEs) as a sustainable medium for developing cost-effective and ecologically friendly nanomaterials has piqued the interest of current researchers. Herein, waste extracts from papaya barks, banana peels, thumba plants, and snail shells were used for synthesizing ZnO nanostructures via a hydrothermal method, followed by calcination at 400 °C. The crystallinity and pure wurtzite phase formation of ZnO nanostructures were confirmed via X-ray diffraction. ZnO nanostructures with various morphologies such as tight sheet-like, spherical, porous sheet-like, and bracket-shaped, comprising small interconnected particles with a highly catalytically active exposed (0001) facet, were observed via field emission scanning electron microscopy and transmission electron microscopy. The formation mechanism of the various morphologies of the ZnO nanostructures was proposed. Ultraviolet-visible spectra showed different absorption band edges of ZnO nanostructures with a bandgap in the range of 3.17-3.27 eV. Photoluminescence studies showed the presence of various defect states such as oxygen and zinc vacancies and oxygen and zinc interstitials on ZnO nanostructures, which are usually observed in traditionally prepared ZnO. The photocatalytic activity of ZnO nanostructures was evaluated under direct sunlight using rhodamine B (RhB) and Congo red (CR) dyes as probe pollutants. Furthermore, prepared ZnO nanostructures could potentially adsorb anionic dyes (e.g., CR) in the absence of light. Superoxide and hydroxide radicals played a vital role in the photocatalytic activity of ZnO. The photocatalyst could be reused for up to three cycles, indicating its stability. Therefore, this study reports the diverse use of AWEs as cost-effective media for nanomaterial synthesis.

Facile synthesis and ultrastrong adsorption of a novel polyacrylamide-modified diatomite/cerium alginate hybrid aerogel for anionic dyes from aqueous environment.

An eco-friendly cationic polyacrylamide (CPAM)-modified diatomite/Ce(III)-crosslinked sodium alginate hybrid aerogel (CPAM-Dia/Ce-SA) was synthesized successfully and characterized by SEM-EDS, XRD, FTIR, UV-Vis and XPS. Adsorption performance, interaction mechanism and reusability of CPAM-Dia/Ce-SA used for the removal of acid blue 113 (AB 113), acid blue 80 (AB 80), acid yellow 117 (AY 117), Congo red (CR) and Direct Green 6 (DG 6) anionic dyes from aqueous media were investigated in detail. The results demonstrate that CPAM-Dia/Ce-SA aerogel is macroscopic polymer hybrid spheres with a particle size of around 1.3 mm, unique undulating mountain-like surface and porous mesostructure, and exhibits outstanding adsorption capacity for anionic dyes and good reusability. The maximum adsorption amounts of AB 113, AB 80, AY 117, CR and DG 6 by CPAM-Dia/Ce-SA were 3008, 1208, 914, 1832 and 1232 mg/g at pH 2.0, 60 min contact time and 25 °C, and corresponding removal efficiency reached individually 97.5, 96.6, 99.7, 99.9 and 98.5 % respectively and were less affected by increasing pH up to 10.0. Dye adsorption behaviour and adsorption processes with spontaneous and exothermic nature were perfectly interpreted by the Langmuir and Pseudo-second-order rate models respectively. Physicochemical and multisite-H-bonding synergies promoted the ultrastrong biosorption of anionic dyes by CPAM-Dia/Ce-SA.

Synthesis of porous calcium-guar gum benzoate nano-biohybrids for sorptive removal of congo red and phosphates from water.

This work aims to develop an eco-sound nano-bio-hybrid sorbent using sustainable materials for sorptive elimination of congo red and phosphates from aquatic environment. An amphipathic biopolymer derivative, high DS guar gum benzoate (GGBN) was used for entrapment of as synthesized calcium carbonate nanoparticles using solvent diffusion nano-precipitation technique. Designer nano-biohybrids were developed upon experimenting with various materials stoichiometry. SEM, XRD and EDX studies confirmed near-uniform impregnation of rhombohedral calcium carbonate crystals throughout the biopolymer matrix. Average pore size distribution and surface area of final product Ca-GGBNC, were estimated from NDLFT and BET methods respectively. Analysis of adsorption findings acquired at study temperature 27 ± 2 °C showed that the maximum adsorption capacity of Ca-GGBNC recorded qmax, 333.33 mg/g for congo red azo dye and that for phosphate was at 500 mg/g. Adsorptive removal was noted and both components followed pseudo second order kinetics. Intra-particle diffusion kinetics investigation disclosed that the boundary layer effect was prominent and the adsorption rates were not solely directed by the diffusion stage. Activation energy, Ea was to be estimated using Arrhenius equation at 56.136 and 47.015 KJ/mol for congo red and phosphates respectively. The calculated thermodynamic parameters(ΔG°, ΔH°, and ΔS°) revealed the spontaneous, feasible and endothermic sorption process. Owing to active surface area, spherical size, functional moiety and porous network, antibacterial properties of nanobiohybrid were persistent and MIC against E. coli and S. aureus were recorded at 200 µg/mL and 350 µg/mL respectively.

A photochemical route in the synthesis and characterization of La2Ti2O7 and La2Ti2O7/AgO films and its evaluation in Congo red degradation and as antibacterial control to Staphylococcus aureus.

In this article, we propose a simple photochemical method to synthesize pure La2Ti2O7 films and La2Ti2O7 films doped with silver at 1.0, 3.0, and 5.0 mol%. After annealing the photo-deposited films at 900 °C, XRD, SEM, and XPS analyses showed the formation of a monoclinic La2Ti2O7 phase and the presence of Ag and AgO in doped samples. Photocatalytic tests for Congo red degradation demonstrated that pure La2Ti2O7 achieved 25.4% degradation, while doped samples reached a maximum of 92.7% degradation. Moreover, increasing silver doping on La2Ti2O7 films significantly reduced the growth of Staphylococcus aureus, indicating potential antibacterial properties. The enhanced photoactivity was attributed to the formation of a type I heterojunction between La2Ti2O7 and AgO, and a degradation mechanism was proposed based on Congo red degradation.

Synthesis and application of manganese-doped zinc oxide as a potential adsorbent for removal of Congo red dye from wastewater.

Synthetic dyes are considered toxic compounds and as such are not easily removed by conventional water treatment processes. This study demonstrated the synthesis of pure and manganese- (Mn), silver- (Ag), and iron- (Fe) doped zinc oxide (ZnO) nanoparticles via the wet chemical route. In particular, it investigated the batch adsorption studies and physiochemical properties of synthesized pure and doped ZnO materials for removing toxic congo red (CR) dye. X-ray diffraction (XRD), Raman spectroscopy, and energy-dispersive X-ray spectroscopy (EDS) confirmed the synthesis of the pure and doped ZnO materials. The batch adsorption investigation revealed adsorption efficiencies of 99.4% for CR dye at an optimal dose of 0.03 g/30 ml for Mn-doped ZnO at a solution pH of 2. The adsorption capacity of each of the synthesized materials was found to be in order Mn-doped ZnO (232.5 mg/g) > Ag-doped ZnO (222.2 mg/g) > pure ZnO (212.7 mg/g) > Fe-doped ZnO (208.3 mg/g). Both pseudo-second-order kinetics model and the Langmuir isotherm model accurately explained the adsorption behaviors of CR dye. As such, Van der Waal interactions, H-bonding, and electrostatic interaction were found to be the adsorption mechanisms responsible for dye removal. In addition, the desorption-regeneration investigation indicated the successful reuse of the exhausted Mn-doped ZnO material for five cycles of CR dye adsorption with an efficiency of 83.1%. Overall, this study has demonstrated that Mn-doped ZnO could be considered a viable adsorbent for the cleanup of dye-contaminated water.

High-efficient and rapid removal of anionic and cationic dyes using a facile synthesized sole adsorbent NiAlFe-layered triple hydroxide (LTH).

It would be extremely momentous to familiarize a low-cost sole adsorbent NiAlFe-layered triple hydroxides (LTHs) having a strong sorption affinity towards both anionic and cationic dyes. Using the urea hydrolysis hydrothermal method LTHs were fabricated and by altering the ratio of participant metal cations the adsorbent was optimized. BET analysis revealed that the optimized LTHs possess an elevated surface area (160.04 m2/g) while TEM and FESEM analysis portrayed the stacked sheets-like 2D morphology. LTHs were employed for the amputation of anionic congo red (CR) and cationic brilliant green (BG) dye. The adsorption study showed that within 20 and 60 min, respectively, maximum adsorption capacities were achieved at 57.47 mg/g and 192.30 mg/g for CR and BG dye. Adsorption isotherm, kinetics, and thermodynamics study revealed that both chemisorptions with physisorptions were the assertive factor for the dye encapsulation. This enhanced adsorption performance of the optimized LTH for the anionic dye is attributed to its inherent anions exchange properties and new bond formation with the adsorbent skeleton. Whereas for the cationic dye, it was because of the formation of strong hydrogen bonds, and electrostatic interaction. Morphological manipulation of LTHs, formulates the optimized adsorbent LTH111, provokes the adsorbent for this elevated adsorption performance. Overall, this study revealed that LTHs have a high potential for the effectual remediation of dyes from wastewater as a sole adsorbent at a low cost.

Facile synthesis and physicochemical characterization of κ-Carrageenan-silver-bentonite based nanocatalytic platform for efficient degradation of anionic azo dyes.

Water pollution due to textile industry effluents is a global concern that warrants versatile research solutions for degrading them, and for a sustainable environment. In the present work, by using the imperative role of nanotechnology, a facile one-pot synthesis has been devised to generate κ-carrageenan capped silver nanocatalyst (CSNC), and was immobilized on 2D bentonite (BT) sheets to generate nanocatalytic platform (BTCSNC) for the degradation of anionic azo dyes. The nanocomposite(s) were physicochemically characterized using UV-Vis, DLS, TEM, FESEM, PXRD, ATR-FTIR, TGA, BET and XPS etc., to obtain insights into the nanocomposite composition, structure, stability, morphology and mechanism of interaction. The obtained CNSC are monodispersed, spherical with a size of 4 ± 2 nm, and were stabilized by the functional groups (-OH, COO‾, and SO3‾) of κ-Crg. The broadening of peak corresponding to basal plane (001) of BT montmorillonite in PXRD spectra established its exfoliation upon addition of CSNC. XPS and ATR-FTIR data evidenced the absence of covalent interactions between CSNC and BT. The catalytic efficiency of CSNC and BTCSNC composites were compared for the degradation of methyl orange (MO) and congo red (CR). The reaction followed a pseudo first order kinetics, and immobilization of CSNC on BT resulted in a 3-4 fold enhancement in degradation rates. The rates achieved for the degradation kinetics are: MO degradation within 14 s (Ka 9.86 ± 2.00 min-1), and CR degradation within 120 s (Ka of 1.24 ± 0.13 min-1). Further, a degradation mechanism has been proposed by analyzing the products identified through LC-MS. The reusability studies of the BTCSNC evidenced the complete activity of the nanocatalytic platform for six cycles, and gravitational separation method for catalyst recycling. In a nutshell, the current study provided an environmentally friendly, sizable, and sustainable nano catalytic platform" for the remediation of industrial wastewater contaminated with hazardous azo dyes".

Adsorption of cationic and anionic dyes onto coffee grounds cellulose/sodium alginate double-network hydrogel beads: Isotherm analysis and recyclability performance.

This work describes the preparation of new eco-friendly adsorbents with a simple method. Gel beads of coffee grounds cellulose (CGC) and sodium alginate (SA) were prepared for wastewater treatment. Upon their synthesis, the physicochemical properties, performances and efficiency were analyzed by means of various structural and morphological characterizations. Kinetic and thermodynamic adsorption approaches evaluated the removal capacity of these beads which reached equilibrium in 20 min for Methylene Blue (MB) and Congo Red (CR). Also, the kinetics shows that the results can be explained by the pseudo-second-order model (PSO). Furthermore, the isotherm assessments showed that Langmuir-Freundlich can fit the adsorption data of both contaminants. Accordingly, the maximum adsorption capacities reached by the Langmuir-Freundlich model are 400.50 and 411.45 mg/g for MB and CR, respectively. It is interesting to note that the bio-adsorption capabilities of MB and CR on bead hydrogels decreased with temperature. Besides, the results of the thermodynamic study evidenced that the bio-adsorption processes are favorable, spontaneous and exothermic. The CGC/SA gel beads are therefore outstanding bio-adsorbents, offering a great adsorptive performance and regenerative abilities.

Fabrication of a corn stalk derived cellulose-based bio-adsorbent to remove Congo red from wastewater: Investigation on its ultra-high adsorption performance and mechanism.

A cellulose-based bio-absorbent with various and plenty of amino groups was successfully prepared from corn stalk to achieve quantitative removal of Congo red from wastewater with wide pH values (5 ≤ pH ≤ 10). The maximum removal amount was 8.0 mmol·g-1 (5572 mg·g-1) under pH = 6.0 and 45 °C, which was obviously higher than reported absorbents. Investigation on dynamic adsorption and recyclability in authentic wastewater found that the removal efficiency of Congo red was >98 % within 180 min and decreased slightly in industrial water after five cycles, denoting this adsorbent with great potential for environmental application. The characterization results proved that 7.58 mmol·g-1 of different amino groups (-NH2, -NH- and -NR2) were introduced on adsorbent surface by two steps of modification and were the major functional groups for adsorption of Congo red. The inferred adsorption mechanism revealed that Congo red could be adsorbed equivalently on the amino groups by strong electrostatic interactions or hydrogen bonds. Different amino groups played different roles in adsorption due to great differences in protonation ability in 5 ≤ pH ≤ 10. The study was expected to high-efficiently remove Congo red from acidic or alkaline wastewater, and offered an alternative strategy for biowaste treatment of corn stalks in a high value-added manner.

Efficient removal of Congo red and methylene blue using biochar from Medulla Tetrapanacis modified by potassium carbonate.

Biochar (BC) prepared from Medulla Tetrapanacis was recognized as having potential in environmental remediation because of its porous texture, abundant chemical surface groups and mineral composition. In this study, a novel modified biochar (KBC) derived from Medulla Tetrapanacis achieved efficient adsorption of Congo red (CR) and methylene blue (MB). Characterization results suggested that the modification had little effect on the group distribution of KBC, but a dramatic expansion of specific surface area was observed on KBC (1180.45 m2/g) compared to BC (198.51 m2/g). KBC exhibited a maximum sorption of 584.17 mg/g for CR and 318.01 mg/g for MB. Kinetic and isotherm studies revealed sorption of CR and MB by KBC was chemosorption, which occurred on the monolayer surface. The comprehensive analysis also provided the basis for the application of KBC to practical production. These outcomes suggested that KBC may become a new option for the effluent treatment.

Utilization of metal industry solid waste as an adsorbent for adsorption of anionic and cationic dyes from aqueous solution through the batch and continuous study.

Industrial waste, for instance, textile effluents when released into the ecological system without first being treated or with inappropriate levels of treatment, can lead to serious issues deteriorating the environment and human health. Moreover, solid waste from various industries has also become a major issue due to massive urbanization. For instance, the waste from the metal industry has been rapidly increasing such as Jarosite which has various metals, metal oxides, and silica in its composition. Therefore, Jarosite was utilized as an adsorbent for the adsorption of anionic Congo red (CR) and cationic Methylene blue (MB) dyes from aqueous solutions. The processed adsorbent sample was characterized by BET, XRD, SEM, EDS, FTIR, and XPS techniques. The effects of initial dye concentration, pH, adsorbent dose, temperature, and contact time were examined. The metal industry waste is used as a low-cost abundant adsorbent with great potential for adsorption ability to remove the CR (97.5%) and MB (68.5%) at pH 7, contact time 90 min, adsorbent dose 0.1 g, and initial dye concentration 50 mg/L. The adsorption data followed the adsorption isotherm and Kinetics for both dyes. The removal of both dyes was a physical adsorption process, endothermic and spontaneous reaction. Column adsorption investigation was described by AB (Adams-Bohart) and YN (Yoon-Nelson) models. According to the economic view, the utilization of jarosite for dye removal is a cost-effective approach, because it is collected free of cost from industries. Henceforth, for the first time, toxic metal industry waste was successfully utilized as an adsorbent for wastewater treatment.

Noval green sodium alginate/gellan gum aerogel with 3D hierarchical porous structure for highly efficient and selective removal of Congo red from water.

Rational design of adsorbed materials with three-dimensional (3D) hierarchical porous structure, sustainable, high adsorption capacity, and excellent selective is of great significance in practical applications. Herein, a novel aerogel adsorbed material with 3D hierarchical porous architecture was fabricated by employing naturally abundant sodium alginate (SA)/gellan gum (GG) as basic construction blocks to achieve sustainability as well as applying polyethyleneimine (PEI) as functional material for highly efficient and selective capture of Congo red (CR). The aerogel sorbent exhibited strong microstructure, numerous active adsorption sites and being ultralight. The resulting aerogel adsorbent showed high adsorption capacity (3017.23 mg/g) toward CR, exceedingly most previously reported sorbents. Furthermore, the aerogel adsorbent was accompanied by outstanding selectivity for CR in four binary dye systems. Meanwhile, after 3 cycles, the adsorption capacity decreased by 14.8 %, but still maintained the adsorption capacity of 559.79 mg/g. Therefore, excellent adsorption performance, and superb selectivity prefigures its great prospects for wastewater purification.

Detection and Typing of Renal Amyloidosis by Fluorescence Spectroscopy Using the Environmentally Sensitive Fluorophore K114.

PURPOSE: To demonstrate that spectral analysis using the K114 fluorophore can detect and differentiate AL and AA renal amyloidosis. PROCEDURES: Kidney biopsies from patients with AL amyloidosis, AA amyloidosis, and normal samples with no evident pathology were stained with Congo Red and K114. The specimens were imaged on a spectral confocal microscope. RESULTS: Congo Red displayed homogeneous spectra across the three tissue types while K114 chromatically distinguished between normal tissue, AL amyloid, and AA amyloid. Additionally, Congo Red displayed an increased risk of false positive staining compared to K114. Spectral phasors computed from K114-stained tissue sections quantitatively differentiated the three tissue types. K114-stained amyloid deposits displayed a significantly greater increase in brightness after 50 images acquired in rapid succession compared to normal tissue. Quantitative analysis of intensity changes in the background of diseased tissue also differentiated AL and AA amyloid samples, suggesting widespread amyloid deposition. Both amyloid and the backgrounds of diseased samples red-shifted while normal tissue blue-shifted in response to repeated imaging, supporting this theory. CONCLUSIONS: K114 staining of renal biopsies is a promising technique to detect and differentiate types of renal amyloidosis. Due to the advantages this method has over traditional Congo Red staining, the techniques presented here warrant further development for potential use in clinical settings.

Photocatalytic removal of organic dye using green synthesized zinc oxide coupled cadmium tungstate nanocomposite under natural solar light irradiation.

In this work, zinc oxide coupled cadmium tungstate (ZnO-CT) was prepared as a nano-photocatalyst through a green synthesis route using lemon leaf extract and characterized based on diverse microscopic and spectroscopic techniques. To explore the applicabilties of the prepared nanocomposite (NC), its photocatalytic activity has been investigated against Congo red (CR) dye under natural solar light irradiation conditions. ZnO- CT nano-photocatalyst showcases 97% photocatalytic degradation of the CR after 90 min of natural solar light irradiation with quantum yield of 1.16 × 10-8 molecules photon-1. The ZnO-CT NC has shown the enhanced photocatalytic degradation performance against CR when compared to its pristine forms (e.g., ZnO (70%) or CT (44%)). According to the free radical trapping and quenching experiments, the photocatalytic activity of ZnO-CT NC appears to be driven efficiently by superoxide and hydroxyl radicals. The photocatalytic degradation kinetics for CR dye was also studied using the pseudo-first-order, diffusional, and Singh models. The high photocatalytic activity of ZnO-CT NC can be accounted for by the presence of electron-withdrawing functional groups like acids (-COOH) and aldehydes (-CHO) on its surface which helped maintain the prolonged recombination of charge carriers and enhanced stability of ZnO-CT (with moderately low leaching rate of cadmium ions (∼2-5%)).

Chitosan functionalized bismuth oxychloride/zinc oxide nanocomposite for enhanced photocatalytic degradation of Congo red.

The industrial discharge of dye pollutant contaminated wastewater is the major cause of water and soil pollution. Photocatalysis is a promising and green remediation technology, which has received widespread attention in the remediation of hazardous dyes from aqueous environment and convert them into harmless compounds. Herein, we report the synthesis of chitosan (CS) functionalized bismuth oxychloride/zinc oxide (BiOCl/ZnO) nanocomposite by a modified hydrothermal route. The physiochemical characterization revealed that the synthesized nanocomposite have crystalline, agglomerated spherical along with rod shaped morphology and size range from 35 to 160 nm. FTIR peaks at 825, 727, 662 and 622 cm-1 specified the presence of BiO and ZnO bonds, whereas peak at 1635 cm-1 revealed the existence of amine groups which confirms the presence of CS in the synthesized CS-BiOCl/ZnO nanocomposite. Catalytic property of synthesized nanocomposite was evaluated by the degradation of Congo red (CR) under UV-light irradiation. CR dye degradation percentage was found to be 93 % within a short period of 40 min by utilizing UV-light. Furthermore, reusability of CS-BiOCl/ZnO photocatalyst was also investigated, and it remained significant photocatalytic activity after three consecutive cycles. Hence, the results obtained in this study revealed that CS-BiOCl/ZnO nanocomposite can be used as a potential photocatalyst to remediate organic pollutants in various industries.

A magnetically recyclable lignin-based bio-adsorbent for efficient removal of Congo red from aqueous solution.

It has been always attractive to design a sustainable bio-derived adsorbent based on industrial waste lignin for removing organic dyes from water. However, existing adsorbent strategies often lead to the difficulties in adsorbent separation and recycling. Herein, we report a novel magnetically recyclable bio-adsorbent of Mg(OH)2/Fe3O4/PEI functionalized enzymatic lignin (EL) composite (EL-PEI@Fe3O4-Mg) for removing Congo red (CR) by Mannish reaction and hydrolysis-precipitation. The Mg(OH)2 and PEI functionalized EL on the surface act as active sites for the removal of CR, while the Fe3O4 allows for the easy separation under the help of a magnet. As-obtained EL-PEI@Fe3O4-Mg forms flower-like spheres and has a relatively lager surface area of 24.8 m2 g-1 which is 6 times that of EL. The EL-PEI@Fe3O4-Mg exhibits a relatively high CR adsorption capacity of 74.7 mg g-1 which is 15 times that of EL when initial concentration is around 100 mg L-1. And it can be easily separated from water by applying an external magnetic field. Moreover, EL-PEI@Fe3O4-Mg shows an excellent anti-interference capability according to the results of pH values and salt ions influences. Importantly, EL-PEI@Fe3O4-Mg possesses a good reusability and a removal efficiency of 92 % for CR remains after five consecutive cycles. It is illustrated that electrostatic attraction, π-π interaction and hydrogen binding are primary mechanisms for the removal of CR onto EL-PEI@Fe3O4-Mg. This work provides a novel sustainable strategy for the development of highly efficient, easy separable, recyclability bio-derived adsorbents for removing organic dyes, boosting the efficient utilization of industrial waste lignin.