Maximum Degradation Research Articles

Optimization of waste biomass demineralization through response surface methodology and enhancement of thermochemical and fusion properties

This study examines the impact of leaching with dilute hydrochloric acid solution on the reduction of ash content and the thermal degradation behavior of sugarcane bagasse. Response surface methodology (RSM) was used to statistically design the experiments and investigate the effect of three independent variables: treatment time, solid-to-liquid ratio, and reagent concentration. The leaching conditions were further optimized and experimentally validated for maximum ash reduction for suitability of treated biomass as feedstock for thermochemical conversion technologies. Reagent concentration and treatment time directly affected ash reduction, while the solid-to-liquid ratio inversely influenced it. Concentration had the highest impact, and treatment duration had the least. The maximum 78.2% ash reduction was achieved by treating the biomass with 1 M HCl for 80 min at a solid-to-liquid ratio of 50:1 (wt/vol). This ash reduction also resulted in a 9.82% increase in higher heating value (HHV). Hemicellulose hydrolysis during leaching was observed through chemical composition and Fourier-transform infrared spectroscopy (FTIR). Ash fusion temperatures increased, indicating more thermally stable biomass. Thermogravimetric analysis (TGA) showed elevated maximum degradation temperature and activation energy.

La-supported SnO2–CaO composite catalysts for efficient malachite green degradation under UV–vis light

This study presents the development and optimization of La@SnO2–CaO composite catalysts for efficient photocatalytic degradation of malachite green dye in aqueous solutions under UV–vis light irradiation. The catalysts were prepared via conventional incipient-wetness impregnation and thoroughly characterized using advanced analytical techniques, including X-ray diffraction, Fourier transform infrared spectroscopy, UV–vis diffuse reflectance spectroscopy, N2 adsorption–desorption analysis, and scanning electron microscopy. To optimize photodegradation efficiency, the effects of three independent factors were systematically investigated using response surface methodology: Temperature, pH, and Sn/Ca molar ratio. Our results reveal optimal conditions for maximum dye degradation: pH 7, Sn/Ca molar ratio of 0.33, and a process time of 35 min, resulting in a maximum photodegradation efficiency of 98.80% for malachite green dye. Notably, visible light exhibited a more pronounced effect on dye degradation compared to UV light over time, with visible light achieving 25% greater dye removal after 60 min of illumination. Furthermore, the catalyst showed excellent recyclability, retaining 85% of its initial activity after five consecutive cycles. These findings contribute significantly to the development of sustainable methods for dye removal from wastewater and highlight the potential of La@SnO2–CaO composite catalysts in environmental remediation processes, particularly in treating textile industry effluents.

Research on Soybean Seedling Stage Recognition Based on Swin Transformer

Accurate identification of the second and third compound leaf periods of soybean seedlings is a prerequisite to ensure that soybeans are chemically weeded after seedling at the optimal application period. Accurate identification of the soybean seedling period is susceptible to natural light and complex field background factors. A transfer learning-based Swin-T (Swin Transformer) network is proposed to recognize different stages of the soybean seedling stage. A drone was used to collect images of soybeans at the true leaf stage, the first compound leaf stage, the second compound leaf stage, and the third compound leaf stage, and data enhancement methods such as image rotation and brightness enhancement were used to expand the dataset, simulate the drone’s collection of images at different shooting angles and weather conditions, and enhance the adaptability of the model. The field environment and shooting equipment directly affect the quality of the captured images, and in order to test the anti-interference ability of different models, the Gaussian blur method was used to blur the images of the test set to different degrees. The Swin-T model was optimized by introducing transfer learning and combining hyperparameter combination experiments and optimizer selection experiments. The performance of the optimized Swin-T model was compared with the MobileNetV2, ResNet50, AlexNet, GoogleNet, and VGG16Net models. The results show that the optimized Swin-T model has an average accuracy of 98.38% in the test set, which is an improvement of 11.25%, 12.62%, 10.75%, 1.00%, and 0.63% compared with the MobileNetV2, ResNet50, AlexNet, GoogleNet, and VGG16Net models, respectively. The optimized Swin-T model is best in terms of recall and F1 score. In the performance degradation test of the motion blur level model, the maximum degradation accuracy, overall degradation index, and average degradation index of the optimized Swin-T model were 87.77%, 6.54%, and 2.18%, respectively. The maximum degradation accuracy was 7.02%, 7.48%, 10.15%, 3.56%, and 2.5% higher than the MobileNetV2, ResNet50, AlexNet, GoogleNet, and VGG16Net models, respectively. In the performance degradation test of the Gaussian fuzzy level models, the maximum degradation accuracy, overall degradation index, and average degradation index of the optimized Swin-T model were 94.3%, 3.85%, and 1.285%, respectively. Compared with the MobileNetV2, ResNet50, AlexNet, GoogleNet, and VGG16Net models, the maximum degradation accuracy was 12.13%, 15.98%, 16.7%, 2.2%, and 1.5% higher, respectively. Taking into account various degradation indicators, the Swin-T model can still maintain high recognition accuracy and demonstrate good anti-interference ability even when inputting blurry images caused by interference in shooting. It can meet the recognition of different growth stages of soybean seedlings in complex environments, providing a basis for post-seedling chemical weed control during the second and third compound leaf stages of soybeans.

Synthesis and characterization of Nd‐TiO2 and Nd‐ZnO nanostructures for photocatalytic degradation of textile wastewater

AbstractThis study was executed on textile wastewater degradation using laboratory‐prepared Nd‐TiO2 and Nd‐ZnO nanostructures by sol–gel and hydrothermal ultrasonication methods, respectively. The synthesized nano‐photocatalysts were fully characterized using XRD, FE‐SEM/EDX, FT‐IR, and UV‐DRS. The XRD analysis shows that TiO2 crystalline size with Nd doping is 6.14 nm with only the anatase phase, whereas ZnO is 29.59 nm. DRS spectra show that the energy band gap of the doped TiO2 nanostructure was 3.16 eV, whereas, in the case of the Nd‐ZnO nanostructure, it was 3.19 eV, which further indicates more photocatalytic activity. Photocatalytic application for textile wastewater degradation was tested regarding biological oxygen demand and chemical oxygen demand. The maximum degradation of textile wastewater at dilution 1:9 was observed to be 96% and 91% for Nd‐TiO2 and 89% and 87% for Nd‐ZnO under UV and solar irradiations, respectively, with the optimized catalyst dose of 0.2 g/L (Nd‐TiO2) and 0.3 g/L (Nd‐ZnO) at a pH of 7.52. The recyclability shows a slight decrease in efficiency throughout five cycles. The photocatalytic activity of Nd‐TiO2 was higher due to the favorable band gap and smaller crystallite size. The findings indicate that solar light may be a long‐term, cost‐effective renewable source for large‐scale wastewater treatment.

Exploration of Pristine ZnO and Cobalt Doped ZnO for the Solar Photocatalytic Degradation of Methylene Blue Dye

The ZnO and Co-doped ZnO were prepared by eco-friendly and modest route, including thermal disintegration of zinc oxalate (ZnOx) and cobalt-zinc oxalate (CoZnOx) powders, respectively, from a mechano-chemical method. The process of conversion of metal/s oxalate dihydrate to the pristine ZnO and cobalt-doped ZnO was studied with TG-DTG and FTIR spectroscopy. ZnO and Co-doped ZnO crystallites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Energy dispersive X-ray (EDX), UV–visible and photoluminescence (PL) spectroscopies. Hexagonal Wurtzite crystallite structures of the aforementioned materials were illustrated from XRD data. The surface morphological investigation was done with SEM. EDX study confirms the elemental purity of materials. Chemical bonding information was obtained from FTIR spectra. Optical properties were studied from UV-visible and photoluminescence spectroscopy. Exploration of pristine ZnO and cobalt-doped ZnO for the solar photocatalytic degradation (PCD) of methylene blue dye has been done in a batch photoreactor. The various related parameters such as photocatalyst amount, initial concentration of dye and pH were also examined for maximum degradation efficiency for mentioned dye.

Breaking New Grounds: solid-state synthesis of TiO2 – La2O3 – CuO Nanocomposites for degrading Brilliant Green dye under Visible Light

Environmental pollution, particularly from industrial dyes and chemicals, poses a significant threat to ecosystems and human health. Traditional pollution mitigation methods are often inefficient and costly. Photocatalysis has emerged as a promising solution for degrading pollutants using light energy. Titanium dioxide (TiO2) is a widely studied photocatalyst due to its stability, non-toxicity, and strong oxidative power. However, its efficiency is limited by a wide bandgap, restricting absorption to the UV region, and rapid electron-hole recombination. To address these limitations, doping TiO2 with materials like La2O3 and CuO has been explored to enhance its photocatalytic activity under visible light. This study investigates the enhancement of TiO2 nanocomposites by incorporating La2O3 and CuO. X-ray diffraction (XRD) revealed that the nanocomposites retained TiO2's anatase and rutile phases with improved crystallinity. Scanning electron microscopy (SEM) displayed spherical nanoparticles forming agglomerates, typically due to high surface energy. Energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) confirmed the presence of La and Cu in the TiO2 matrix. Fourier-transform infrared (FTIR) spectroscopy identified characteristic vibrational modes of Ti–O, La–O, and Cu–O bonds, suggesting strong chemical interactions between dopants and TiO2 lattice. Ultraviolet-visible (UV-Vis) spectroscopy showed a red shift in absorption spectra with La2O3 and CuO addition, reducing the bandgap energy from 3.23 eV (pure TiO2) to 2.27 eV for the TiO2–0.1La2O3–0.2CuO composite. Photoluminescence (PL) spectroscopy indicated improved charge separation and reduced electron-hole recombination rates in the synthesized nanocomposites. Photocatalytic performance was evaluated by degrading Brilliant Green (BG) dye under visible light. The TiO2–0.1La2O3–0.2CuO (TLC0.2) nanocomposite achieved a maximum dye degradation of over 95% after 204 minutes under optimal conditions (C0 = 17 mg/L and a S/L ratio of 1 g/L). Adding the inorganic agent Na2SO4 to this process significantly enhanced photocatalytic activity, increasing degradation from 56% to 95% after 180 min of visible light irradiation under C0 = 20 mg/L and S/L = 0.5 g/L conditions, as it shows a high stability after six reuse cycles. In conclusion, La2O3 and CuO doping significantly enhance TiO2 nanocomposites' crystalline structure, morphology, optical properties, and photocatalytic efficiency, demonstrating their potential for environmental remediation and solar energy conversion.

Carbon defect induced electron transfer promotes electrocatalytic activation of molecular oxygen to selectively generate singlet oxygen for pollutants removal

This study explored the design of heterojunctions incorporating defective graphene and boron nitride (BN) to activate molecular oxygen (O₂) and degrade sulfamethoxazole (SMX) by establishing efficient electron transport channels. These heterojunction catalysts, designed using theoretical predictions, were synthesized by controlling carbon defect concentration and pyrolysis temperature. The optimized GBN cathode achieved a maximum SMX degradation rate of 0.0252min⁻¹, with a total organic carbon (TOC) removal efficiency of 47.31%. Singlet oxygen (¹O₂) was identified as the primary reactive oxygen species, exhibiting a generation rate of 18.66μMmin⁻¹ and contributing 93.5% to SMX degradation. Results demonstrated that an optimal defect concentration enhances electron transfer, promoting the 2-electron reduction of O₂ to H₂O₂ and facilitating further H₂O₂ activation, thereby accelerating SMX degradation. This work advances the development of non-metallic cathodic catalysts and provides valuable insights into electrochemical degradation mechanisms for organic pollutants.

Simultaneous dehalogenation and oxidation of dichloroacetamide by Cu-modified CoFe-LDH in three-dimensional continuous flow aerated electrocatalytic reactor

Searching for catalysts and degradation systems for synchronous dehalogenation and oxidation of haloacetamides (HAcAms) is pressing. In this study, a novel three-dimensional continuous flow aerated electrocatalytic reactor (3D CFAER) system, which employed Cu-modified CoFe layered double hydroxides (CoFe-LDH) composite/activated carbon as a catalytic particle electrode for the degradation of dichloroacetamide (DCAcAm) was constructed. Under the experiment’s optimal operating parameters, the maximum degradation rate of DCAcAm reached 91.7 %. The superior performance for the degradation of DCAcAm was due to the enhanced electron transfer induced by the modification of Cu in CoFe-LDH. Moreover, Density Functional Theory (DFT) calculations indicated that Cu doping improved the ability of LDH to dissociate water, thereby enhancing its electrocatalytic performance. Scavenger experiments and Electron Paramagnetic Resonance (EPR) results revealed that •OH, O2•– and electrochemical direct dehalogenation were responsible for DCAcAm removal. Additionally, the electrocatalytic stability of the electrode was tested upon repeated use with DCAcAm degradation remaining as high as 81.7 % after five consecutive experiments. More importantly, in 3D CFAER, electrocatalytic treatment lasting 90 min reduced the TOC and COD of the actual chlorine disinfection wastewater by 64.1 % and 74.9 %, respectively. This study provides new theoretical basis and technical support for control of HAcAms.

A multifunctional coconut shell biochar modified by titanium dioxide for heavy metal removal in water/soil and tetracycline degradation

Heavy metals and tetracycline pollute the environment and endanger human health. This work prepared a multifunctional coconut shell biochar (Ti-XBC) through NaHCO3 activation and TiO2 modification. The modified coconut shell biochar was characterized by various methods. Ti-4BC exhibited excellent removal performance for heavy metals. The maximum adsorption capacity of Ti-4BC on Cd2+, Pb2+, Cr3+, and Cr6+ reached 104.2, 136.8, 101.2, 112.4 mg/g in water. The adsorption of Ti-4BC for four metal ions had a competitive effect in the binary metal system. It also reduced the mobility of four heavy metal ions in soil. Density functional theory (DFT) calculations were employed to explain the mechanism of heavy metal removal. Additionally, the degradation performance and mechanism of Ti-4BC towards tetracycline were investigated. The results indicated that the maximum degradation rate was 99.4%. Overall, this work developed a multifunctional material capable of both removing heavy metals and degrading antibiotics, addressing the issue of single-function in biochar. This provided a novel approach for tackling complex and diverse environmental pollution scenarios.

Tiempos de cosecha sobre el valor nutritivo del forraje verde hidropónico de cebada

The aim of this study was to evaluate the effect of harvest days (16, 18, 20 and 22 after germination) on the nutritional value of hydroponic green forage (HGF) of barley in terms of chemical composition: dry matter (DM ), organic matter (OM), crude protein (CP), mineral matter (MM) and neutral detergent fibre (NDF), and the determination of the kinetic parameters of the in situ degradation of DM and CP, using three cattle with fistula rumen. The incubation times were: 0, 6, 12, 24, 48 and 72 hours. The DM and MM were similar (p>0.05) in the cultures, while the highest CP concentration was observed on day 16 and 18 (15.07 and 14.66%, respectively). NDF decreased linearly due to the effect of harvest days. The day factor quadratically influenced the degradation of the soluble fraction (SF) of the DM and PC, estimating 60 and 62.53% as maximum degradation of SF at 17 and 15 days of harvest, respectively. On the contrary, the potentially degradable fraction (PFD) of DM and CP decreased by 15.91 and 12.88% at 19 and 13 days of germination, respectively. The potential degradability of the DM was high and different on days 16 and 18, and with higher and similar values ​​in the effective degradability for the passage rates of 2, 5 and 8%/hour in relation to the other days. The same behaviour was recorded in the CP passage rates. The FVH of barley at 16 and 18 days after germination has a higher CP content, lower indigestible fractions of DM and CP and high effective degradability, which allows these crops to be classified as feeds of high nutritional quality that favour their use as a supplement for ruminants.

Investigating the synergistic effects of carbon and glass fibers on the mechanical and thermal properties of phenol‐containing phthalonitrile composites

AbstractThe progressive development of lightweight composites exhibiting desirable thermo‐mechanical properties is an area of growing interest, particularly with the phthalonitrile (PN) based composites, which have shown great potential. However, our understanding of the mechanical and thermal properties of the phenol‐containing phthalonitrile (PN75) resin composites often reveals limitations that make them less suitable for specific structural applications. In this work, we focused on enhancing the mechanical and thermal properties of the PN75 resin through the incorporation of the 4‐aminophthalonitrile (4‐APN), resulting in improved the curing behaviors and increased thermal stability. Our investigation of the short carbon fiber (SCF) and short glass fiber (SGF) reinforced PN75 resin composites revealed that the hybrid SCF/SGF‐based composites at 15 wt% SCF and 15 wt% SGF content exhibited an excellent tensile and the flexural strength. Additionally, the thermogravimetric analysis demonstrated maximum onset degradation and decomposition temperatures at this ratio compared with the neat resin, also we evaluated the interfacial adhesion properties of the SCF/SGF and the PN75 resin composites. These findings contribute to the advancement of polymer composite materials and expand their potential applications across various industries.

Improved mechanical, thermal, and barrier properties of halloysite nanotubes and nanocellulose incorporated PVA-PEO films: For food packaging applications

This work presents a novel polyvinyl alcohol (PVA)-polyethylene oxide (PEO) nanocomposite with halloysite nanotube (HNT)-nanocellulose (NC) hybrid filler to tailor the mechanical, thermal, and barrier properties. PVA-PEO/ HNT-NC nanocomposites are characterized using various analytical techniques such as FTIR, XRD, TGA, DSC, and SEM. The study evaluated the impact of hybrid filler on water vapor transmission rate (WVTR), moisture retention capacity (MRC), peroxide value (POV), and mechanical properties. The simultaneous application of 3 wt% HNT and 5 wt% NC resulted in a 20 % increase in tensile strength and approximately two-fold increase in Young's modulus, with a maximum degradation temperature increase of 22° C and 16° C in the second and third stages, respectively. Compared to the pure blend, the nanocomposite exhibited a 67 % (26.7 ± 0.6 mEq/kg) improvement in oxygen barrier performance, while maintaining a low WVTR and good MRC, demonstrating their suitability for packaging applications.

Optimization of Photocatalytic Degradation of Rhodamine B and Indigo Carmine Dyes Using Eco‐Friendly Kaolinite‐Silver Oxide Quantum Dots Nanocomposite Under Sunlight Irradiation

ABSTRACTIn this work, we present a simple method for the pyrofabrication of a new kaolinite‐ silver oxide quantum dots nanocomposite (Kao‐Ag2O/QDs) that is used for the degradation of rhodamine B (RhB) and indigo carmine (IC) dyes. A homogenous combination of kaolinite and silver nitrate was sintered up to 350 °C to create the extremely effective photocatalyst (Kao‐Ag2O/QDs). Various analytical techniques were employed to characterize the Kao‐Ag2O/QDs photocatalyst such as XRD, FTIR, XPS, SEM–EDX, TEM, DTA/TGA, ZP, BET, and UV–Vis DRS. The degradation of RhB and IC dyes through the photocatalyst was carried out in aqueous solutions utilizing several pH dye solutions and sustainable solar energy in atmosphere conditions. The nanocomposite that was prepared had shown an enhanced specific surface area of 53.3005 m2/g, a pore size of 8.1197 nm, and a total pore volume of 0.216 cm3/g. It also displayed an optical band gap energy of 2.9 eV. The study creates that employing the ideal dose of 2000 and 1500 mg/L of the Kao‐Ag2O/QDs photocatalyst at neutral conditions (pH = 7) resulted a maximum degradation effectiveness of RhB and IC of 91.06 and 93.46% after 90 min, respectively. RhB and IC dyes degradation followed Langmuir first‐order kinetics with a rate constant of 0.0217 and 0.0216 min−1 at pH = 7, respectively. The photocatalytic degradation activity for RhB dye is based on hydroxyl radicals (˙OH) and superoxide radicals (˙O2−), while the mechanism of IC removal is based on superoxide radicals (˙O2−), as revealed by scavenger‐based radical trapping studies. A triple reusability study found that the Kao‐Ag2O photocatalyst is highly stable with degradation efficiencies of RhB and IC dyes from the initial 91.09 to 90.04, 88.54, and 86.27% and from the initial 93.46 to 92.8, 91.4 and 89.32%, respectively. The optimal situations for the parameters were identified by the Box–Behnken design (BBD), which was well matched with photocatalytic degradation tests.

Isolation and degradation characterization of a 1, 4-dioxane-degrading bacterial strain

To address the potential pollution caused by the carcinogen 1, 4-dioxane in aquatic environments, we isolated a highly efficient 1, 4-dioxane-degrading bacterial strain, designated as DXTK-010, from the groundwater contaminated by 1, 4-dioxane. According to the morphological characteristics, the phylogenetic tree established based on the 16S rRNA gene sequence, and the whole genome sequence, we identified DXTK-010 as Aminobacter aminovorans. This strain demonstrated robust degradation capacity within a temperature range of 20 ℃ to 37 ℃ and a pH range of 5.0 to 8.0. Furthermore, single-factor experiments indicated the optimal degradation conditions at 30 ℃ and pH 7.5. Under the optimal conditions, the strain completely degraded 200 mg/L of 1, 4-dioxane within 24 h, achieving a maximum degradation rate of 9.367 mg/(L·h). The Monod equation was adopted to fit the degradation kinetics of 1, 4-dioxane at different initial concentrations, which revealed a maximum specific degradation rate of 0.224 mg 1, 4-dioxane/(mg protein·h), a half-saturation constant (Ks) of 41.350 mg/L, and a cell yield of 0.130 mg protein/(mg 1, 4-dioxane). Whole genome sequencing revealed a circular chromosome and three plasmids within DXTK-010. Functional gene annotation and analysis underscored the significance of the propane monooxygenase gene cluster and alcohol dehydrogenase gene in facilitating the efficient degradation of 1, 4-dioxane by this strain. DXTK-010 outperformed the existing degraders for 1, 4-dioxane, expanding the strain resources for the bioremediation of 1, 4-dioxane pollution. This study provides a theoretical basis for the practical application of DXTK-010 in the remediation of 1, 4-dioxane pollution.

Isolation and Characterization of Novel Cellulose Micro/Nanofibers from Lygeum spartum Through a Chemo-Mechanical Process.

Recent studies have focused on the development of bio-based products from sustainable resources using green extraction approaches, especially nanocellulose, an emerging nanoparticle with impressive properties and multiple applications. Despite the various sources of cellulose nanofibers, the search for alternative resources that replace wood, such as Lygeum spartum, a fast-growing Mediterranean plant, is crucial. It has not been previously investigated as a potential source of nanocellulose. This study investigates the extraction of novel cellulose micro/nanofibers from Lygeum spartum using a two-step method, including both alkali and mechanical treatment as post-treatment with ultrasound, as well as homogenization using water and dilute alkali solution as a solvent. To determine the structural properties of CNFs, a series of characterization techniques was applied. A significant correlation was observed between the Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) results. The FTIR results revealed the elimination of amorphous regions and an increase in the energy of the H-bonding modes, while the XRD results showed that the crystal structure of micro/nanofibers was preserved during the process. In addition, they indicated an increase in the crystallinity index obtained with both methods (deconvolution and Segal). Thermal analysis based on thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) confirmed improvement in the thermal properties of the isolated micro/nanofibers. The temperatures of maximum degradation were 335 °C and 347 °C. Morphological analysis using a scanning electron microscope (SEM) and atomic force microscope (AFM) showed the formation of fibers along the axis, with rough and porous surfaces. The findings indicate the potential of Lygeum spartum as a source for producing high-quality micro/nanofibers. A future direction of study is to use the cellulose micro/nanofibers as additives in recycled paper and to evaluate the mechanical properties of the paper sheets, as well as investigate their use in smart paper.

Evaluation of photocatalytic efficiency of TiO2 applied over cement plaster for mitigating urban air pollutant: TVOC

Photocatalysis emerged as a prominent method for mitigating air pollution stemming from emissions of total volatile organic compounds (TVOCs) in both indoor and outdoor environments. Given the slow degradation rate of certain TVOCs, which pose health risks, including carcinogenicity, there is a pressing need for effective air purification strategies, particularly within built environments where individuals spend substantial amounts of time. This study delves into the efficacy of TiO2 photocatalysis in reducing air pollutants when applied to building surfaces. Cement mortar samples, incorporating varied doses of TiO2 ranging from 7.83E-03 g/cm2 to 4.92E-02 g/cm2, were prepared and examined within batch reactors, both under sunlight exposure and in the absence thereof, to gauge their degradation rates towards TVOCs. Furthermore, surface characterization techniques were employed to explicate the microstructural properties of TiO2-coated plastered samples. The results obtained demonstrated the variation in the rate of degradation from 1.09E-04±0.1 % to 3.1E-4 ± 1.13 % min−1cm−2 for various initial concentrations of total volatile organic compounds (TVOCs) in the range of 600 ppm to 2900 ppm over a period of 100 min. The selected approach demonstrated the maximum degradation rate constant of 5.2E-04 min−1cm−2 corresponding to 15 % of TiO2 dose by weight of cement. These findings underscore the promise of TiO2 in purifying polluted air and advocate for its widespread implementation on building surfaces to enhance air quality.

By-product distribution and cytotoxicity assessment of ZnO-assisted photocatalytic degradation of reactive blue 250 dye

This research examined the effectiveness and feasibility of utilizing ultraviolet (UV) assisted photo-catalysis to treat wastewater effluents from textile production containing reactive blue 250 (RB 250) dye. Molecular oxygen and active species like O2•−, HO2•, H2O2 and •OH play crucial roles in the degradation process. Additionally, the degradation of dyes is influenced by several factors, including dye concentration, duration of UV irradiation, pH levels, concentration of H2O2, and the catalyst. The concentration of H2O2 and catalyst dose for the decolorization was studied at 0.6 mL and 0.5 g respectively. The discoloration was higher at low dye concentration, high H2O2 concentration, acidic conditions and high catalyst concentration. The maximum degradation (97 %) of RB 250 dye was obtained in the presence of zinc oxide nanoparticles within 90 min. The extent of decolorization of the dye was determined by UV–Vis spectroscopy. Fourier transform infrared spectroscopy (FTIR) was employed to analyze the changes in functionalities after degradation. The disappearance of characteristic peaks associated with specific groups within the dye molecule confirmed the extensive degradation of RB 250 dye. LCMS analysis was conducted to examine the intermediates and a mechanistic degradation pathway was subsequently proposed. The cytotoxicity of the irradiated dye samples was evaluated through a hemolytic test both pre and post-treatment. The findings suggest that the UV/H2O2/ZnO treatment represents a promising approach for effectively degrading RB 250 dye.

Synergistic bioremediation of petroleum-contaminated soil using immobilized consortium of Rhodococcus rhodochrous and Bacillus subtilis laccase

Petroleum-contaminated soil represents a significant environmental and public health challenge on a global scale. Microbial bioremediation has shown potential, yet the role of enzymes in enhancing petroleum degradation remains underexplored. In this study, the synergistic effects of Rhodococcus rhodochrous (R.rh) and Bacillus subtilis-derived laccase (BsLac) was investigated in the remediation of petroleum-contaminated soil. Immobilized R.rh (PSIMRH) and BsLac (ADIMLac) exhibited higher petroleum degradation rates than their free state, achieving 78.3% and 56.3% degradation in liquid systems, respectively. The combined treatment of PSIMRH and ADIMLac demonstrated a synergistic effect on petroleum degradation, achieving 43.6% with a maximum degradation constant of 0.0335 d−1, representing a 202.7% improvement over untreated soil. PSIMRH enhanced petroleum degradation through microbial metabolism, while ADIMLac accelerated the initial breakdown of complex hydrocarbons into simpler, more bioavailable ones via enzymatic oxidation, providing growth substrates for microbes and significantly improving petroleum degradation rates. The microbial analysis revealed an increase abundance of known petroleum-degrading bacterial genera, including Rhodococcus, Lysobacter, Micromonospora, and Streptomyces. However, the presence of BsLac appeared to reduce the competitive advantage of Rhodococcus, promoting the proliferation of indigenous strains like Lysobacter and Streptomyces. These results suggest that enzyme-microbe synergy can enhance the bioremediation process by altering microbial community dynamics and accelerating petroleum degradation. This study attempts to remediate petroleum-contaminated pollution with the combined use of strains and enzymes, providing a new approach for the remediation of other pollution problems.

Evaluating physico-mechanical properties of NaOH-treated natural fibres: Effects of polyolefin

The bottle gourd plant fibres (BGPF) and okra fibres were processed and refined (w/w 6 % NaOH) before being incorporated with polyolefin (polypropylene) for composite fabrication using a blending technique. The polyolefin matrix is used to develop composites with 5 % okra fibres and varying percentages (25, 30, 35 and 40 %) of BGPF. The results indicated that the "35 % BGPF +5 % okra +60 % polypropylene" composition achieved remarkable mechanical properties with tensile strength (26.95 MPa), tensile modulus (3.16 GPa), decreased elongation at break (1.71 %), bending strength (52.53 MPa), bending modulus (3.45 GPa), impact strength (14.25 kJ/m2), and hardness (69 D-shore). Moreover, these composites absorbed minimal water when a specific portion was submerged. The scanning electron microscopy (SEM) test on the composites revealed good fibre adhesion and adherence content between BGPF and okra fibres. Additionally, the thermo-gravimetric analysis and differential scanning calorimetry exhibited weight loss of composites during maximum cellulose degradation (80 %) at 483 °C. In the composites of the fibre-PP matrix, two distinct physical changes were observed indicating glass transition and degradation. However, the mechanical properties decreased after soil degradation. Thus, remarkable properties were achieved for the fibres-fibres and fibres-polyolefin (polypropylene) interfacial interactions.

Saraca asoca-assisted green synthesise of ZnO nanoplatelets for photocatalytic activity and adsorption kinetics

ABSTRACT ZnO nanoplatelets (ZnO NPLs) have been successfully synthesised using microwave-assisted technique (400 W, 180 sec) with the plant extract Saraca-asoca. The surface morphology analysis confirms ZnO’s plate-like nanostructure, leading to the creation of ZnO NPLs. The results show excellent photocatalytic performance (at 125 W for both UV and visible light) and effectiveness against malachite green (MG), methyl orange (MO) and rhodamine B (RhB). Notably, ZnO NPLs break down malachite green (MG) exceptionally well, reaching a maximum degradation efficiency of 92% in under 30 min (UV light). Moreover, ZnO NPLs have been evaluated for MG adsorption characterised by the pseudo-first-order kinetic model, alongside the Freundlich and Langmuir isotherm models. In the Freundlich model, the maximal adsorption capacity is determined to be 331 mg/g. These new faceted ZnO NPLs have a great potential for use in photocatalytic and adsorption processes that aim to reduce aqueous pollutants.