Aqueous phase adsorption of phenothiazine derivative onto zinc oxide doped activated carbon.

Plant-mediated synthesis of nanoparticles is a sustainable approach that has gained widespread scientific acceptance due to its numerous benefits and applications. In this study, a zinc oxide-doped activated carbon (ZAC) derived from palm kernel shells (PKS) was synthesized via a bioreduction route using a water-based extract of Nymphaea lotus leaves as a reducing agent. The synthesized ZAC nanocomposites were characterized using microscopic (TEM, SEM) and spectroscopic (FTIR, EDS, XRD, and UV-Vis) analyses. The adsorptive properties of ZAC and efficiency in scavenging a phenothiazine derivative (methylene blue) from an aqueous solution were investigated. Results reveal that nano-scale ZAC particles were crystalline, exhibited irregular shapes, with an average size of 45 nm, and were highly dispersed. The optimum quantity adsorbed was 248 mg/g at a methylene blue concentration of 140 mg/L for 60 min using 0.02 g/100 mL of ZAC. Adsorption and kinetics data closely aligned with the Freundlich isotherm and the pseudo-second-order model, respectively indicating heterogeneous surface adsorption and chemisorption as the dominant mechanisms. The regeneration study of ZAC shows that over five cycles, thermal regeneration maintained high adsorption capacity with minimal decline and chemical regeneration significantly led to reduction in the adsorption capacity but solvent washing offered a balance between efficacy and structural preservation.

Exploring the superior adsorption capacity of multi-layer graphene/alginate granules for the removal of methylene blue dye from water.

Graphene-based materials are gaining increasing attention towards their use in manufacturing and environmental applications. In this context, multi-layer graphene (MG) has been recently applied for the adsorption of contaminants from water resulting in promising results. However, the extreme lightness of this material often makes it difficult to handle due to its potential dispersion in the surrounding environment as well as to its transport and loss with the effluent. In this study, a novel granular material was synthesized by embedding MG into an alginate matrix, resulting in the so-called granular MG (GMG). This material was tested for the adsorption of methylene blue (MB) from water, which is a typical dye used in textile industries and must be removed from the effluent. GMG materials with different MG contents (5 and 20 %) were compared with MG and a commercial adsorbent to assess their adsorption capacity and the most performing material was selected for in-depth physical and chemical characterization. The structural, surface, kinetic, isotherm, and thermodynamic properties, the pH and temperature dependence, as well as the regeneration and reuse of GMG 5% were investigated through batch adsorption tests under different operating conditions. The study reveals that GMG 5% has a superior adsorption capacity compared to the tested materials and can be considered as a promising alternative to commercial carbon-based materials according to techno-economic considerations.

Adsorption parameters optimization of spent coffee ground biochar for methylene blue removal using response surface methodology.

This study investigates the potential of spent coffee ground biochar (SCGB) as a sustainable and cost-effective adsorbent for the removal of methylene blue (MB), a hazardous dye commonly used in the textile and printing industries. A response surface methodology (RSM) approach with central composite design (CCD) was employed to systematically investigate the effects of key process parameters, including adsorbent dosage, solution pH, contact time and temperature, on MB removal efficiency. The analysis revealed that adsorbent dosage and temperature as critical factors influencing MB removal, with a linear model providing a strong correlation. Optimal conditions for MB removal were determined to be 0.99 g of SCGB, 30 min of contact time, 30 °C temperature, and a solution pH of 7. Under these conditions, MB removal reached 99.99%, with a desirability of 1.000. The experimental results closely matched the predicted values, differing by only 0.02%, thus validating the accuracy of the model. Kinetic studies indicated a rapid adsorption process, well-described by both pseudo-first and pseudo-second order models. Isotherm analysis confirmed the applicability of the Freundlich model, suggesting favorable adsorption with increasing MB concentration. The high adsorption capacity of SCGB is attributed to its carbonaceous and porous structure, highlighting its potential as an effective adsorbent for dye removal in wastewater treatment applications.

Tailoring ZnS nanostructures through precipitation-cum-hydrothermal synthesis for enhanced wastewater purification and antibacterial treatment.

This study presents a novel blend of synthesis techniques for shape-controlled ZnS nanoparticles. Zinc sulfide (ZnS) nanoparticles with distinct morphologies cauliflower-like microstructures (∼4.5 µm) and uniform nanospheres (200-700 nm) were synthesized through an innovative blend of precipitation and hydrothermal techniques. Capping with polyvinylpyrrolidone (PVP) significantly decreased crystallite size (3.93 nm-2.36 nm), modulated the band gap (3.57 eV-3.71 eV), and dramatically influenced morphology, highlighting the novelty of shape-controlled synthesis and its impact on optoelectronic and functional properties. X-ray diffraction confirmed crystallinity and revealed the size-controlling influence of PVP. UV-vis spectroscopy suggested potential tuning of optical properties due to band gap widening upon PVP capping. Field-emission scanning electron microscopy (FESEM) unveiled distinct morphologies: cauliflower-like microstructures for ZnS and uniform nanospheres (200-700 nm) for PVP-ZnS. Both structures were composed of smaller spherical nanoparticles, demonstrating the role of PVP in promoting controlled growth and preventing agglomeration. High-resolution transmission electron microscope (HRTEM) images depicted that the majority of nanoparticles maintain a spherical shape, though slight deviations from perfect sphericity can be discerned. Fourier-transform infrared (FTIR) spectroscopy confirmed that successful PVP encapsulation is crucial for shaping nanospheres and minimizing aggregation through steric hindrance. Photocatalytic activity evaluation using methylene blue (MB) dye degradation revealed significantly faster degradation by PVP-ZnS under ultraviolet (UV) irradiation (within 60 min as compared to 120 min for ZnS), showcasing its superior performance. This improvement can be attributed to the smaller size, higher surface area, and potentially optimized band gap of PVP-ZnS. Additionally, PVP-ZnS exhibited promising antibacterial activity against S. aureus and P. aeruginosa, with increased activity at higher nanoparticle concentrations.

Efficient Removal of Methylene Blue Dye from Aqueous Media Using Facilely Synthesized Magnesium Borate/Magnesium Oxide Nanostructures.

Methylene blue dye in water sources can pose health risks to humans, potentially causing methemoglobinemia, a condition that impairs the blood's ability to carry oxygen. Hence, the current study investigates the synthesis of novel magnesium borate/magnesium oxide (Mg3B2O6/MgO) nanostructures and their efficiency in removing methylene blue dye from aqueous media. The nanostructures were synthesized using the Pechini sol-gel method, which involves a reaction between magnesium nitrate hexahydrate and boric acid, with citric acid acting as a chelating agent and ethylene glycol as a crosslinker. This method helps in achieving a homogeneous mixture, which, upon calcination at 600 and 800 °C, yields Mg3B2O6/MgO novel nanostructures referred to as MB600 and MB800, respectively. The characterization of these nanostructures involved techniques like X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, N2 gas analyzer, and field-emission scanning electron microscope (FE-SEM). These analyses confirmed the formation of orthorhombic Mg3B2O6 and cubic MgO phases with distinct features, influenced by the calcination temperature. The mean crystal size of the MB600 and MB800 samples was 64.57 and 79.20 nm, respectively. In addition, the BET surface area of the MB600 and MB800 samples was 74.63 and 64.82 m2/g, respectively. The results indicated that the MB600 sample, with its higher surface area, generally demonstrated better methylene blue dye removal performance (505.05 mg/g) than the MB800 sample (483.09 mg/g). The adsorption process followed the pseudo-second-order model, indicating dependency on available adsorption sites. Also, the adsorption process matched well with the Langmuir isotherm, confirming a homogeneous adsorbent surface. The thermodynamic parameters revealed that the adsorption process was physical, exothermic, and spontaneous. The MB600 and MB800 nanostructures could be effectively regenerated using 6 M HCl and reused across multiple cycles. These findings underscore the potential of these nanostructures as cost-effective and sustainable adsorbents for methylene blue dye removal.

Chitosan extraction from Amanita phalloides: yield, crystallinity, degree of deacetylation, azo dye removal and antibacterial properties.

Chitosan, a biopolymer obtained from chitin, is known for its remarkable adsorption abilities for dyes, drugs, and fats, and its diverse array of antibacterial characteristics. This study explores the extraction and characterization of chitosan from the mycelium of Amanita phalloides. The moisture content, ash content, water binding capacity, fat binding capacity, and degree of deacetylation of the extracted chitosan were determined. The chitosan exhibited a high yield of 70%, crystallinity of 49.07%, a degree of deacetylation of 86%, and potent antimicrobial properties against both Gram-negative and Gram-positive bacteria. The study also examined the adsorption capabilities of chitosan to remove methylene blue (MB) dye by analysing specific factors like pH, reaction time, and MB concentration using the response surface model. The highest degree of MB dye removal was 91.6% at a pH of 6, a reaction time of around 60 min and an initial dye concentration of 16 ppm. This experimental design can be applied for chitosan adsorption of other organic compounds such as dyes, proteins, drugs, and fats.

One-pot synthesis of g-C3N4/N-doped CeO2 nanocomposites and their potential visible light-driven photocatalytic degradation of methylene blue dye.

In the pursuit of efficient photocatalytic materials for environmental applications, a new series of g-C3N4/N-doped CeO2 nanocomposites (g-C3N4/N-CeO2 NCs) was synthesized using a straightforward dispersion method. These nanocomposites were systematically characterized to understand their structural, optical, and chemical properties. The photocatalytic performance of g-C3N4/N-CeO2 NCs was evaluated by investigating their ability to degrade methylene blue (MB) dye, a model organic pollutant. The results demonstrate that the integration of g-C3N4 with N-doped CeO2 NCs reduces the optical energy gap compared to pristine N-doped CeO2, leading to enhanced photocatalytic efficiency. It is benefited from the existence of g-C3N4/N-CeO2 NCs not only in promoting the charge separation and inhibits the fast charge recombination but also in improving photocatalytic oxidation performance. Hence, this study highlights the potential of g-C3N4/N-CeO2 NCs as promising candidates for various photocatalytic applications, contributing to the advancement of sustainable environmental remediation technologies.

Blended Nephelium lappaceum and Durio zibethinus wastes for activated carbon production via microwave-ZnCl2 activation: optimization for methylene blue dye removal.

Herein, this work targets to employ the blended fruit wastes including rambutan (Nephelium lappaceum) peel and durian (Durio zibethinus) seed as a promising precursor to produce activated carbon (RPDSAC). The generation of RPDSAC was accomplished through a rapid and practical procedure (microwave-ZnCl2 activation). To evaluate the adsorptive capabilities of RPDSAC, its efficacy in eliminating methylene blue (MB), a simulated cationic dye, was measured. The Box-Behnken design (BBD) was utilized to optimize the crucial adsorption parameters, namely A: RPDSAC dose (0.02-01 g/100 mL), B: pH (4-10), and C: time (2-6 min). The BBD design determined that the highest level of MB removal (79.4%) was achieved with the condition dosage of RPDSAC at 0.1 g/100 mL, contact time (6 min), and pH (10). The adsorption isotherm data is consistent with the Freundlich concept, and the pseudo-second-order versions adequately describe the kinetic data. The monolayer adsorption capacity (qmax) of RPDSAC reached 120.4 mg/g at 25 °C. Various adsorption mechanisms are involved in the adsorption of MB dye onto the surface of RPDSAC, including π-π stacking, H-bonding, pore filling, and electrostatic forces. This study exhibits the potential of the RPDSAC as an adsorbent for removal of toxic cationic dye (MB) from contaminated wastewater.

Effectiveness of sentinel lymph node biopsy and bilateral pelvic nodal dissection using methylene blue dye in early-stage operable cervical cancer-A prospective study.

OBJECTIVE: To evaluate the effectiveness of methylene blue dye in detecting sentinel lymph nodes (SLNs) in women with early-stage operable (defined as FIGO I-IIA) cervical cancer. It also aims to evaluate procedural challenges and accuracy. METHOD: This prospective study, which focused on 20 women with early-stage cervical cancer, was carried out between June 2016 and December 2017. These patients had SLN mapping with methylene blue dye injections and thorough examinations, including imaging. All patients underwent radical hysterectomy and complete bilateral pelvic lymphadenectomy. No additional investigation was done on the lymph node in cases where a metastasis was found in the first H&E-stained segment of the sentinel node. RESULT: 20 patients were included in the analysis. The median age of the subjects was 53, and 95 % of them had squamous cell carcinoma. 90 % of the time, the identification of SLNs was effective, and 55 SLNs were found, of which 52.7 % were on the right side of the pelvis and 47.3 % on the left. The obturator group had the most nodes, followed by the external and internal iliac groups in descending order of occurrence. Metastasis was detected in 3 patients, resulting in a sensitivity of 100 % and a specificity of 93.75 % for SLN biopsy. Notably, no false-negative SLNs were found. Complications related to methylene blue usage included urine discoloration in 30 % of patients. CONCLUSION: This trial highlights the promising efficacy and safety of methylene blue dye alone for SLN identification in early-stage operable cervical cancer, with a notably higher success rate. Despite limitations like a small sample size, healthcare professionals and researchers can build upon the insights from this study to enhance cervical cancer management.

Application of chemically modified waste tucumã (Astrocaryum aculeatum) seeds in the biosorption of methylene blue: kinetic and thermodynamic parameters.

Dye effluents cause diverse environmental problems. Methylene blue (MB) dye stands out since it is widely used in the textile industry. To reduce the pollution caused by the MB, we developed biosorbents from tucumã seeds, where the in natura seeds were treated with NaOH (BT) and H3PO4 (AT) solutions and characterized by Boehm titration, point of zero charges, FTIR, TGA, BET, and SEM. It was observed that the acid groups predominate on the surface of the three biosorbents. The process was optimized for all biosorbents at pH = 8, 7.5 g/L, 240 min, C0 = 250 mg/L, and 45 ℃. BT was more efficient in removing MB (96.20%; QMax = 35.71 mg/g), while IT and AT removed around 60% in similar conditions. The adsorption process best fits Langmuir and Redlich-Peterson isotherms, indicating a hybrid adsorption process (monolayer and multilayer) and pseudo-second-order kinetics. Thermodynamic data confirmed an endothermic and spontaneous adsorption process, mainly for BT. MB was also recovered through a desorption process with ethanol, allowing the BT recycling and reapplication of the dye. Thus, an efficient and sustainable biosorbent was developed, contributing to reducing environmental impacts.

Removal of Methylene Blue Dye from Aqueous Solutions Using Polymer Inclusion Membrane Containing Calix[4]pyrrole.

The effective purification of aqueous solutions of methylene blue dye was tested using polymer inclusion membranes (PIMs) that contained cellulose triacetate (CTA) as a polymer base, o-nitrophenyl octyl ether (o-NPOE) as a plasticizer, and meso-tetra methyl tetrakis-[methyl-2-(4-acetlphenoxy)] calix[4]pyrrole (KP) as a carrier. Scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy were used to define the microstructure and surface of PIMs. Experimental results showed that, with an increased concentration of methylene blue in an aqueous solution, the removal percentage also increased. Further observation showed that the flux increased with the rise in the source phase pH values from 3 to 10. The carrier and plasticizer content in the membrane significantly influenced the membrane's transport properties. The optimal composition of the membrane in percent by weight for KP was 74% plasticizer; 18% support, and 8% carrier. The maximum MB removal (93.10%) was achieved at 0.10 M HCl solution as the receiving phase. It was shown that the membrane with optimal composition showed good reusability and enabled the easy and spontaneous separation of methylene blue from aqueous solutions.

Neem biomass derived carbon quantum dots synthesized via one step ultrasonification method for ecofriendly methylene blue dye removal.

This article presents a one-step ultrasonication technique for generating biomass carbon dots (BCDs) from neem bark (Azadirachta indica) powder. The BCDs were characterized using modern techniques such as UV-Vis, FTIR, Raman, XRD, HRTEM, FESEM, EDAX, and Zeta potential analyses. Unlike traditional nanocomposite bed systems, this study utilized BCDs as a liquid-phase adsorbent for the regenerative adsorption of the environmentally harmful dye, methylene blue (MB), through an in-situ precipitation reaction. This involved the formation of BCDs-MB adduct via an electrostatic mechanism. The adsorption capacity and percentage of removal were remarkable at 605 mg g-1 and 64.7% respectively, exceeding various solid-based adsorption methods in the literature. The Langmuir isotherm and pseudo-second-order kinetics model provided an excellent fit for this system. The calculated thermodynamic parameter, Gibbs free energy change (ΔG) was negative, indicating a spontaneous, exothermic, and physisorption-based mechanism. The regenerative capacity of our system was further demonstrated by successfully extracting and recovering the MB dye (64%) using ethyl alcohol as the solvent. This method provides an efficient means of recovering valuable cationic organic dye compounds from contaminated environments.

Sn(IV)porphyrin-Incorporated TiO2 Nanotubes for Visible Light-Active Photocatalysis.

In this study, two distinct photocatalysts, namely tin(IV)porphyrin-sensitized titanium dioxide nanotubes (SnP-TNTs) and titanium dioxide nanofibers (TNFs), were synthesized and characterized using various spectroscopic techniques. SnP-TNTs were formed through the hydrothermal reaction of NaOH with TiO2 (P-25) nanospheres in the presence of Sn(IV)porphyrin (SnP), resulting in a transformation into Sn(IV)porphyrin-imbedded nanotubes. In contrast, under similar reaction conditions but in the absence of SnP, TiO2 (P-25) nanospheres evolved into nanofibers (TNFs). Comparative analysis revealed that SnP-TNTs exhibited a remarkable enhancement in the visible light photodegradation of model pollutants compared to SnP, TiO2 (P-25), or TNFs. The superior photodegradation activity of SnP-TNTs was primarily attributed to synergistic effects between TiO2 (P-25) and SnP, leading to altered conformational frameworks, increased surface area, enhanced thermo-chemical stability, unique morphology, and outstanding visible light photodegradation of cationic methylene blue dye (MB dye). With a rapid removal rate of 95% within 100 min (rate constant = 0.0277 min-1), SnP-TNTs demonstrated excellent dye degradation capacity, high reusability, and low catalyst loading, positioning them as more efficient than conventional catalysts. This report introduces a novel direction for porphyrin-incorporated catalytic systems, holding significance for future applications in environmental remediation.

Preoperative localisation of parathyroid adenomas using ultrasound-guided methylene blue dye injection.

Purpose: Primary hyperparathyroidism is mainly caused by parathyroid adenomas. Preoperative imaging can be performed using different imaging modalities, e.g. ultrasound (US), radionuclide scanning, magnetic resonance imaging, and computed tomography, often used in combination. Currently, US-guided blue dyes, especially methylene blue (MB) injection, are used to identify parathyroid tumours. Material and methods: This was a retrospective study of 228 patients. Preoperative ultrasound, scintigraphy, and bio-chemistry were performed on all patients, and fine-needle aspiration procedures were performed on suspected patients. Using preoperative US-G injection with MB dye, target tumours were injected in all cases. Results: A total of 163 patients were female and 65 were male. The mean age was 42.5 years. US was positive in 203 (89%) cases, 25 (11%) were negative, and all had a positive sestamibi scan (100%). US-G needle injections with MB dye of target tumours were successful in all cases. The average diameter of the lesions was 18 mm. All had positive intraoperative identification of parathyroid adenoma and MB staining (100% accuracy, 100% sensitivity, and 100% specificity). Operating time (min ± SD) was 22.7 ± 11.5 minutes, and the success rate was 100%. All were parathyroid adenomas histologically. Intraoperative parathormone hormone decreased in all patients. In postoperative follow-up, all were normocalcaemic with no local or systemic complications. Conclusions: Localisation of small parathyroid adenomas by US-guided blue dye injection is a safe, simple, and useful tool when performing parathyroidectomy with no complications.

Green synthesis of carbon quantum dots from teak leaves biomass for in situ precipitation and regenerative-removal of methylene blue-dye.

The objective of this study was to completely eliminate environmentally harmful cationic organic dye from aqueous solutions using the one-step ultrasonication method, renowned for its energy efficiency, user-friendliness, and minimal requirement for chemical resources, making it particularly suitable for large-scale applications. To achieve effective environmental remediation, we employed carbon dots derived from teak leaf biomass (TBCDs) layered with graphene oxide. We conducted a thorough characterization of the TBCDs using UV-vis spectroscopy (with absorption peaks at λmax = 208 and 276 nm), FTIR spectroscopy (confirming the presence of various functional groups including -OH, -CH, C = O, COO-, C-O-C, and = C-H), Raman spectroscopy (with bands at 1369 cm-1 (D-Band) and 1550 cm-1 (G-Band), and an intensity ratio (ID/IG) = 0.88, indicating structural defects correlated with the sp3 hybridization sites on the TBCDs), XRD analysis (indicating an amorphous nature of particles), HRTEM imaging (showing homogeneous dispersal of TBCDs with typical sizes ranging from 2 to 10 nm), FESEM analysis (showing a flat surface and minuscule particles), and Zeta potential analysis (revealing a surface charge peak at -51.0 mV). Our adsorption experiments yielded significant results, with a substantial 50.1 % removal rate and an impressive adsorption capacity of 735.2 mg g-1. Theoretical adsorption parameters were rigorously analyzed to understand the adsorption behavior, surface interactions, and mechanisms. Among these models, the Langmuir isotherm in conjunction with pseudo-second-order kinetics provided an exceptional fit (with R2 values closer to 1) for our system. The Gibbs free energy (ΔG) was found to be negative at all temperatures, indicating the spontaneity of the reaction. Regarding mechanism, electrostatic attraction ((+ve) MB dye + (- ve) TBCDs), π-π stacking adsorption facilitated by the graphitic structure, formation of multiple hydrogen bonds due to polar functional groups, and a pore-filling mechanism wherein the cationic MB dye fills the pores of TBCDs with graphene oxide layers, forming an adduct were identified. Furthermore, we demonstrated the regenerative capacity of our system by effectively extracting and recovering the MB dye (with a regeneration rate of 77.1%), utilizing ethyl alcohol as the solvent. These findings not only provide valuable insights into the adsorption capabilities of TBCDs but also highlight the potential of our approach in the recovery of expensive cationic organic dye compounds from polluted environments.

Exploring the potential of a Ephedra alata leaf extract: Phytochemical analysis, antioxidant activity, antibacterial properties, and green synthesis of ZnO nanoparticles for photocatalytic degradation of methylene blue.

Ephedra alata leaf extracts have therapeutic properties and contain various natural compounds known as phytochemicals. This study assessed the phytochemical content and antioxidant effects of a Ephedra alata leaf extract, as well as zinc oxide (ZnO) nanoparticle production. The extract contained phenolic acids, including vanillic acid, chlorogenic acid, gallic acid, p-coumaric acid, vanillin and rutin. Its total phenolic content and total flavonoid content were 48.7 ± 0.9 mg.g-1 and 1.7 ± 0.4 mg.g-1, respectively. The extract displayed a DPPH inhibition rate of 70.5%, total antioxidant activity of 49.5 ± 3.4 mg.g-1, and significant antimicrobial activity toward Gram-positive and negative bacteria. The synthesized ZnO nanoparticles had spherical shape, crystallite size of 25 nm, particle size between 5 and 30 nm, and bandgap energy of 3.3 eV. In specific conditions (90 min contact time, pH 7, and 25°C), these nanoparticles efficiently photodegraded 87% of methylene blue, suggesting potential applications for sustainable water treatment and pollution control.

Comparative study of synthesis methods and pH-dependent adsorption of methylene blue dye on UiO-66 and NH2-UiO-66.

Metal-organic frameworks (MOFs) are highly promising adsorbents with notable properties such as elevated adsorption capacities and versatile surface design capabilities. This study introduces two distinct synthesis methods, one lasting 1 h and the other 24 h, for UiO-66 and NH2-UiO-66. While both methods yield structures with comparable crystallinity and morphology, the adsorption performance of the cationic methylene blue dye varies at different pH levels. Despite the 24 h synthesis time being optimal for maximum adsorption in both MOFs, the relative difference in NH2-UiO-66 adsorption percentage at different times suggests reduced dependency on synthesis time for this property. Notably, NH2-UiO-66 exhibits consistent and effective performance across three pH levels, warranting further investigation into its adsorption kinetics and isotherm. The achievement of high adsorption efficiency coupled with a significantly reduced synthesis time underscores the importance of developing simplified synthetic methods, essential for enhancing the practical applicability of MOFs in diverse applications.

A comparative study on green synthesis and characterization of Mn doped ZnO nanocomposite for antibacterial and photocatalytic applications.

Biological and green synthesis of nanomaterial is a superior choice over chemical and physical methods due to nanoscale attributes implanted in a green chemistry matrix, have sparked a lot of interest for their potential uses in a variety of sectors. This research investigates the growing relevance of nanocomposites manufactured using ecologically friendly, green technologies. The transition to green synthesis correlates with the worldwide drive for environmentally sound procedures, limiting the use of traditional harsh synthetic techniques. Herein, manganese was decorated on ZnO NPs via reducing agent of Withania-extract and confirmed by UV-spectrophotometry with highest peak at 1:2 ratio precursors, and having lower bandgap energy (3.3 eV). XRD showed the sharp peaks and confirms the formation of nanoparticles, having particle size in range of 11-14 nm. SEM confirmed amorphous tetragonal structure while EDX spectroscopy showed the presence of Zn and Mn in all composition. Green synthesized Mn-decorated ZnO-NPs screened against bacterial strains and exhibited excellent antimicrobial activities against gram-negative and gram-positive bacteria. To check further, applicability of synthesized Mn-decorated Zn nanocomposites, their photocatalytic activity against toxic water pollutants (methylene blue (MB) dye) were also investigated and results showed that 53.8% degradation of MB was done successfully. Furthermore, the installation of green chemistry in synthesizing nanocomposites by using plant extract matrix optimizes antibacterial characteristics, antioxidant and biodegradability, helping to build sustainable green Mn decorated ZnO nanomaterial. This work, explains how biologically friendly Mn-doped ZnO nanocomposites can help reduce the environmental impact of traditional packaging materials. Based on these findings, it was determined that nanocomposites derived from biological resources should be produced on a wide scale to eradicate environmental and water contaminants through degradation.

Sustainable production of activated carbon from indigenous Acacia etbaica tree branches employing microwave induced and low temperature activation.

Growing demand for activated carbon as an efficient and cost effective means of treating environmental pollution necessitates the economical production of good quality activated carbon. It is possible if it is done using low cost precursor materials and economical production methods. In the present study, two types of activated carbon were produced from Acacia etbaica tree branches while employing phosphoric acid as an activating agent. The first sample underwent carbonization by microwave irradiation (AC-MWI), while the second sample was carbonised in a furnace (AC-CA). Characterization of the formed activated carbon samples was executed by proximate and ultimate analysis adopting standard ASTM procedures. In addition to the elemental analysis, hardness, bulk density, pH, moisture and ash content, surface morphology, BET specific surface area, pore volume, volatile matter, fixed carbon, and iodine number were determined. Characteristics of both activated carbon samples were compared with the characteristics of activated carbon available in the literature and activated carbon available commercially in the market. The comparison revealed that the characteristics of the produced activated carbon samples was well comparable with the activated carbons produced from other species of Acacia tree and activated carbon available commercially. Results showed that the produced activated carbon demonstrated high activation efficiency of 39.8% and 48.7% for AC-CA and AC-MWI, respectively. Furthermore, AC-MWI has a BET specific surface area higher than that of AC-CA (1065 m2/g and 773 m2/g respectively). It was found that the BET specific surface area and pore volume of AC-MWI was higher by 37.7% and 12.7%, respectively, as compared to the values acquired for AC-CA. Additionally, activated carbon could be produced by microwave irradiation in about 48% less time as compared to traditional low temperature heating. The adsorption study of produced the activated carbon was performed utilising methylene blue (MB) as a contaminant, and the data was fitted to Langmuir, Freundlich, as well as Harkins-Jura isotherm showing comparable correlation. However, Freundlich isotherm was found to be the best to elaborate the MB adsorption on the produced activated carbon. The results confirmed the viability of microwave irradiation in producing good quality activated carbon from Acacia etbaica tree branches, which demonstrated comparable characteristics with commercially available activated carbon. The strategy could be beneficial for the country in order to produce high quality activated carbon and strengthen its self-reliance.

Expermental investigation on adsorption of methylene blue dye from waste water using corncob cellulose-based hydrogel.

Hydrogel from corncob cellulose was synthesized in this investigation. The synthesized Hydrogel was characterized by SEM, XRD, and FTIR instruments. As the results indicate the synthesized hydrogel has required and important features, these suggest the suitability of hydrogel for the adsorption of methylene blue dye (MBD). Three important process variables (dosage, contact time, and initial concentration) with three levels were studied during the adsorption process at 30 °C and neutral pH. The efficiency of hydrogel for adsorption of MBD was determined in each experiment. The experimental results were statistically analyzed and interpreted. The maximum removal efficiency was achieved at 2.22 g/L of dosage, 80.36 min of contact time, and 74.54 mg/L of initial concentration. At this condition, 98.25% of MBD was achieved through experimental tests. Kinetics, isotherm, and thermodynamics studies were performed. Langmuir isotherm is more suitable to describe the adsorption process and the Pseudo second-order kinetic model fits this process. From the thermodynamics studies, all negative values of change in Gibbs free energy (ΔG°), and positive value of change in enthalpy (ΔH°), and change in entropy (ΔS°) indicate that the carried out experimental process is a spontaneous and endothermic. Moreover, the regeneration experiment for adsorbent was performed. The treatment of real textile industry waste water was conducted and the removal efficiency of hydrogel was 64.76%. This removal percentage reduction from sythetic aqueous solution is due to involvement of other pollutants in the real waste water. The synthesized hydrogel adsorbent is suitable up to the third cycle without significant loss in removal efficiency.