Dye Concentration Research Articles

Sugarcane peel ash as a sorbent for methylene blue

Sugarcane peel waste (SPW) modified by combustion was used as a sorbent for methylene blue (MB) in aqueous medium under the influence of parameters such as pH of the medium, initial MB concentrations, contact time, SPW dosage, and temperature using batch experiments. The microstructure of the adsorbent was analyzed using Fourier infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), and X-ray diffractometer (XRD). The quantity (mg/g) of adsorbed MB increased with increased contact time, rise in dye concentration, as well as the solution pH. Similarly, the temperature of the system improved the sorption effectiveness with maximum sorption capacity of 65.4 and 81.2% at 45 °C and 55 °C for USPW and MSPW, respectively. At an initial MB concentration of 100 mg/L, temperature of 45 °C and 55 °C, pH of 4, and reaction times of 80 and 60 min for unmodified sugarcane peel waste (USPW) and modified sugarcane peel waste (MSPW), respectively, optimal MB adsorption of 22.6 and 33.2 mg g-1, respectively, was achieved.

Preparation of grafted starch‐based cationic flocculants and its removal of reactive and disperse dyes

AbstractIn this paper, a starch‐based flocculant (ADSt) with medium and low temperature solubility and enhanced flocculation effect was synthesized using corn starch, acrylamide, and dimethyldiallyl ammonium chloride as main materials by the ethanol‐alkali method and grafting method. The main mechanism of ADSt's flocculation was electrical neutralization and bridging. The flocculation performance of ADSt was verified by using it along with polymeric aluminum chloride (PAC) as coagulant/flocculant, dispersible dye (dispersible yellow RGFL), and reactive dye (active trimeric blue KN‐G) to simulate dye wastewater. For the dispersed yellow water sample and active emerald blue water sample, the dosage of PAC was 40 and 35 mg/L respectively. When the dosage of ADSt was 10 mg/L with a dye content of 100 mg/L, the decolorization rates for both dyes reached up to 96.2% and 94.4% respectively. The properties of the flocs such as size and two‐dimensional fractal structure were described. The prepared ADSt maintained a good flocculation effect in the pH range of 5–9 due to its excellent water solubility achieved through the ethanol‐alkali preparation process, where its solubility reached 86.7% at 30°C. Overall, the preparation process for ADSt is simple, cost‐effective, while providing an effective solution for treating printing and dyeing wastewater.

Biofabrication of highly effective and easily regenerated CuO nanoparticles as adsorbents for Congo red and malachite green removal

An effective and easily regenerated adsorbent is the one for which scientists are making an effort to explore. In this study, copper oxide nanoparticles (CuO NPs) were synthesized in a green manner from a leaf extract of Moringa stenopetala and used for dye adsorption. XRD, FTIR, and SEM were employed for the characterization of CuO NPs. The crystallite size of the CuO NPs was calculated via Debye–Scherrer equation from the XRD data and was found to be 8.33 nm. The Cu–O bonding bending vibration at 1116 cm− 1 and stretching vibration at 1649 cm− 1 observed from the FTIR data strongly confirmed the formation of CuO NPs. SEM morphology analysis confirmed the formation of nanoparticles with a plate-like morphology and a spherically random orientation. The zero-point charge of CuO NPs was investigated and reported to be at pH 7. The adsorption of dyes on the greenly produced CuO NPs was studied by optimizing different adsorption parameters. The removal efficiencies of the green CuO NPs adsorbent were 99.54% at the optimum conditions (pH, 4; dye concentration, 30 mg/L; amount of adsorbent, 0.25 g; and contact time, 80 min) and 98.33% at the optimum conditions (pH, 11; dye concentration, 20 mg/L; amount of adsorbent, 0.4 g; and contact time, 80 min) for congo red and malachite green, respectively. The adsorption efficiency of the biosynthesized CuO NPs for the mixture of the two dyes was 92.3%. The green synthesized adsorbent was regenerated and able to work effectively for four cycles for the two dyes. The results of the kinetics-type investigation indicate that the adsorption of both dyes by the CuO NPs adsorbent best fits a pseudo-second-order model. The isotherm model-type investigation resulted in the fitting of the Langmuir adsorption isotherm for both the congo red and malachite green dyes.

Synergistic Effect of NiAl-Layered Double Hydroxide and Cu-MOF for the Enhanced Photocatalytic Degradation of Methyl Orange and Antibacterial Properties

This study synthesized NiAl-layered double hydroxide (LDH)/Cu-MOF photocatalyst using a simple impregnation method involving NiAl-LDH and Cu-MOF. The successful synthesis was confirmed through Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), zeta potential measurements, thermogravimetric analysis (TGA), ultraviolet diffuse reflectance spectroscopy (UV-DRS), N2 adsorption at −196 °C, and electrochemical impedance spectroscopy (EIS). Photocatalysts based on NiAl-LDH, Cu-MOF, and NiAl-LDH/Cu-MOF were used to remove methyl orange (MO) dye from contaminated water. The impact of various factors, including pH, dye concentration, and photocatalyst amount, on MO degradation efficiency was assessed. FTIR analysis was conducted both before and after dye degradation. The optimal degradation conditions were a photocatalyst dose of 25 mg and a pH of 3. Kinetic studies indicated that the degradation of MO dye onto NiAl-LDH/Cu-MOF followed a pseudo-first-order and an L–H or Langmuir–Hinshelwood model. The value of R2 = 0.94 confirms the validity of pseudo-first-order and Langmuir–Hinshelwood (L–H) kinetic models for the photocatalytic degradation of MO dye. This study highlights the importance of developing novel photocatalysts with improved degradation efficiency to protect the water environment. Antibacterial activity was also performed with antibacterial sensibility testing by disk diffusion to determine minimal inhibitory and bactericidal concentrations. In short, NiAl-LDH/Cu-MOF can be helpful for various biomedical and industrial applications.

Improvement of electro-Fenton process by using heterogeneous Fe-MIL-88B nanocatalyst and simultaneous rotation of cathode and anode for dye removal

In this study, improvement of the electro-Fenton process using Fe-MIL-88B along with the innovation in the reactor with the simultaneous rotation of the cathodes and anodes was carried out to remove Acid Blue 25. For this purpose, the Fe-MIL-88B nanocatalyst was synthesised by the thermal solvent method and was characterised by FT-IR, EDAX, XRD, and FESEM. For the experiments, an electrochemical cell with a useful volume of 1 L and rotating cathodes and anodes were used and nanoparticles were added to the system as a slurry. To determine the appropriate values of the effective parameters, the OFAT method was used. According to the results, 0.3 g/L Fe-MIL-88B, pH equal to 3, dye concentration of 75 mg/L, a current intensity of 0.228 A, and a rotation velocity of 100 rpm were chosen as suitable values for the process. In optimal conditions, the dye removal efficiency reached to 92.3% after 90 min, which resulted in a 14.5% improvement in the dye removal efficiency compared to the conventional process under the same conditions. Also, after 90 min, the removal efficiencies of 77.08 and 63.63% were obtained for COD and TOC, respectively. The results indicated acceptable decomposition of the effluent into less hazardous compounds.

Nanomodified bamboo (Phyllostachys aurea) biomass: its adsorbent features in the removal of dyes from water under high salinity conditions.

The effluent generated by textile industries is among the most polluting to the environment. Dyes such as methylene blue (MB) and indigo blue (IB) are used in cotton dyeing. This work proposes to evaluate the potential of in natura (BIN) and nanomodified (BNP) bamboo (Phyllostachys aurea) biomass as biosorbents for the removal of MB and IB dyes in an aqueous medium under high salinity conditions. These materials were characterized by Fourier transform infrared (FTIR) and X-ray (XRD) spectroscopies and scanning electron microscopy (SEM) to investigate their morphology and interaction with the dyes and the nanoparticles. The FTIR spectra revealed the existence of hydroxyl and carbonyl groups, ethers, phenols, and aromatic compounds, indicating the presence of a lignocellulosic structure. XRD and SEM analyses confirmed the effectiveness of the nanocomposite synthesis process. The dyes were quantified by ultraviolet-visible spectroscopy (UV/Vis). The material's pH at the point of zero charge (pHPZC) was 5.52 (BIN) and 4.84 (BNP), and the best IB and MB sorption pH were 3.0 and 9.0 for BNP, respectively, employing 30min of contact time. The material sorption capacity (Qexp) was assessed using batch procedures, in which 100-1000mg/L dye concentrations were tested with a 0.5g/L adsorbent dose. The dye's Qexp for BIN and BNP was 25.41 ± 0.58 and 23.42 ± 0.07mg/g (MB) and 84.26 ± 1.1 and 130.81 ± 0.20mg/g (IB), respectively. The kinetic model that best fit BNP experimental data was the pseudo-2nd-order with r2 = 0.99868 (MB) and r2 = 0.99873 (IB), and Freundlich, D-R, and Temkin isotherms best fit the dye sorption data. The bamboo nanomodification facilitates the biosorbent removal from the medium after sorption, enabling large-scale studies and industrial applications-the investigated materials provided promising adsorption features for removing contaminant dyes in saline water.

EDTA‐modified cellulose from sago bark (Metroxylon sagu) for anionic and cationic dyes removal

AbstractThe present research employed ethylenediaminetetraacetic (EDTA) modified cellulose to remove basic violet 10 (BV10) and reactive orange 16 (RO16) dyes. The cellulose was obtained from sago bark which was solid waste of sago starch industries. Sago bark contains 56.86% cellulose so that it can provide significant amount of active site. The optimum condition was examined using batch method investigating some parameters including pH, initial dye concentration, contact time, and thermodynamics. The adsorption capacity of cellulose (Cell) itself was also investigated for the comparison. The characterization of adsorbent showed the presence of ester bond, amine groups and escalating of surface area and pores after EDTA modification. The adsorption capacity of EDTA‐modified cellulose (Cell‐EDTA) was 73.53 mg/g for BV10 and 22.42 mg/g for RO16. The adsorption of both dyes onto Cell‐EDTA followed Langmuir isotherm model and pseudo‐second‐order kinetic model. Thermodynamic parameters indicated that the adsorption process was spontaneous, endothermic and feasible. Desorption studies proved that NaOH was an effective desorbing agent of BV10 and RO16. Based on research, Cell‐EDTA was more favorable in cationic dye, basic violet 10 than anionic dye, reactive orange 16.

A Sustainable Solution for the Adsorption of C.I. Direct Black 80, an Azoic Textile Dye with Plant Stems: Zygophyllum gaetulum in an Aqueous Solution.

The presence of pollutants in water sources, particularly dyes coming by way of the textile industry, represents a major challenge with far-reaching environmental consequences, including increased scarcity. This phenomenon endangers the health of living organisms and the natural system. Numerous biosorbents have been utilized for the removal of dyes from the textile industry. The aim of this study was to optimize discarded Zygophyllum gaetulum stems as constituting an untreated natural biosorbent for the efficient removal of C.I. Direct Black 80, an azo textile dye, from an aqueous solution, thus offering an ecological and low-cost alternative while recovering the waste for reuse. The biosorbent was subjected to a series of characterization analyses: scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET) method, X-ray diffraction (XRD), and infrared spectroscopy (IR) were employed to characterize the biosorbent. Additionally, the moisture and ash content of the plant stem were also examined. The absorption phenomenon was studied for several different parameters including the effect of the absorption time (0 to 360 min), the sorbent mass (3 to 40 g/L), the pH of the solution (3 to 11), the dye concentration (5 to 300 mg/L), and the pH of the zero-charge point (2-12). Thermodynamic studies and desorption studies were also carried out. The results showed that an increase in plant mass from 3 to 40 g/L resulted in a notable enhancement in dye adsorption rates, with an observed rise from 63.96% to 97.08%. The pH at the zero-charge point (pHpzc) was determined to be 7.12. The percentage of dye removal was found to be highest for pH values ≤ 7, with a subsequent decline in removal efficiency as the pH increased. Following an initial increase in the amount of adsorbed dye, equilibrium was reached within 2 h of contact. The kinetic parameters of adsorption were investigated using the pseudo-first-order, pseudo-second-order and Elovich models. The results indicated that the pseudo-first-order kinetic model was the most appropriate for the plant adsorbent. The isotherm parameters were determined using the Langmuir, Frendlich, Temkin, and Dubinin-Radushkevich models. The experimental data were more satisfactory and better fitted using the Langmuir model for the adsorption of dye on the plant. This study demonstrated that Zygophyllum gaetulum stems could be employed as an effective adsorbent for the removal of our organic dye from an aqueous solution.

Physiological and biomolecular interventions in the bio-decolorization of Methylene blue dye by Salvinia molesta D. Mitch

Methylene blue, a cationic dye as a pollutant is discharged from industrial effluent into aquatic bodies. The dye is biomagnified through the food chain and is detrimental to the sustainability of aquatic flora. Despite of number of physico-chemical techniques of dye removal, the use of aquatic flora for bio-adsorption is encouraged. Thus, we used Salvinia molesta D. Mitch in bio-reduction of methylene blue on concentrations of 0, 10, 20, and 30 mg L−1 through 5 days with biosorption kinetics. The dye removal was concentration-dependent, maximized at 2 days with 30 mg L−1 which altered the relative growth rate (44%) of plants. Biosorption recorded 71% capacity at optimum pH (8.0), 24 h reducing major bond energies of amide, hydroxyl groups, etc. Bioaccumulation of dye changed potassium content (446%) under maximum dye concentration modifying tissues for dye sequestration. Reactive oxygen species were altered on dye reduction by oxidase (33%) with redox homeostasis by enzymes. Plants altered the metabolism with over accumulation of polyamines (51%), abscisic acids (448%), and phosphoenolpyruvate carboxylase (83%) on dye reduction. Thus, this study is rationalized with a sustainable approach where aquatic ecosystems can be decontaminated from dye toxicity with the exercise of bioresources like Salvinia molesta D. Mitch as herein.

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

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

Enhanced adsorption of malachite green (MG) dye using RF glow oxygen plasma-modified coconut carbon shell: A sustainable approach for effluent treatment

The textile industry produces dye pollutants that are both harmful and difficult to degrade. This study explores the enhanced adsorption of Malachite Green (MG) dye using coconut carbon shells treated with RF glow oxygen plasma discharge. Plasma treatment improved the surface properties of the adsorbent by introducing oxygen-containing functional groups and increasing surface polarity, which boosted dye adsorption through hydrogen bonding, electrostatic interactions, and π-π stacking. Experimental results revealed that a 10-minute plasma treatment optimally enhanced adsorption capacity by 39 % compared to untreated samples. The Langmuir isotherm model demonstrated a maximum adsorption capacity (qm) of 161 mg/g, surpassing the Freundlich model. At pH 8, using 0.2 g of adsorbent in 50 mL solutions with initial dye concentrations of 25 mg/L and 100 mg/L, the 10-minute plasma-treated samples achieved adsorption capacities of 6.01 mg/g and 23.95 mg/g, respectively, compared to 4.72 mg/g and 17.2 mg/g for the untreated samples. This corresponded to removal efficiencies of 96.12 % and 95.8 % for the treated samples, and 75.6 % and 68.8 % for the untreated samples, after 80 min of contact at 200 rpm. UV–vis spectrophotometry confirmed the reduction in dye concentration after adsorption. FE-SEM analysis revealed that plasma treatment created micro-pores on the coconut carbon shell, enhancing adsorption capacity, while SEM-EDX analysis showed increased oxygen content after 10 min of treatment. FTIR analysis identified additional carbonyl (-C=O) and hydroxyl (-OH) groups, indicating the incorporation of oxygen-containing functional groups due to plasma treatment. Confocal Raman microscopy was also used to analyze the microstructural changes in the samples.

Advanced nano modification of ecofriendly glauconite clay for high efficiency methylene blue dye adsorption

This research focuses on the utilization of nano glauconite clay as an environmentally friendly sorbent for the removal of cationic dyes, particularly Methylene Blue (MB), from polluted water. The glauconite clay was sourced from the El Gidida region of Egypt and subjected to grinding in a laboratory-type ball mill to ensure homogeneity and increase the active sites available for the adsorption process. The resulting ball milled nano clay (BMNC) was characterized using techniques such as X-ray fluorescence (XRF), Fourier transform infrared (FT-IR) spectroscopy, transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD). The concentration of MB dye was monitored using UV–Vis spectroscopy to assess the adsorption capacity of BMNC under various conditions including pH, time, dose, and temperature. The optimal conditions for the adsorption process were determined to be a pH range of 7–8, a contact time of 60 min, and a dose of 200 ppm, resulting in an adsorption capacity of 128 mg/g. This process demonstrated both low cost and high speed. The adsorption mechanism of MB on the BMNC surface was evaluated through kinetics, adsorption isotherms, and thermodynamics. The experimental data indicated an endothermic, spontaneous, and thermodynamically favourable adsorption process, which was further supported by simulated modelling results using Forcite program. The in-silico data aligned well with the experimental findings. Additionally, the study assessed the interference of salts, metal ions, and other dyes on MB adsorption onto BMNC, showing promising results. These findings strongly support the effectiveness of our sorbent substrate under challenging conditions.

Selective adsorption of cationic dye by κ-carrageenan-potato starch bio-hydrogel: Kinetics, isotherm, and thermodynamic studies

An eco-friendly κ-carrageenan/potato starch bio-hydrogel is designed for the efficient removal of methylene blue (MB) dye from water. The incorporation of potato starch was successfully confirmed through XRD, FT-IR, and SEM analysis, while TGA highlighted the hydrogel's thermal stability. Batch adsorption experiments demonstrated excellent MB removal efficiency, with a maximum adsorption capacity of 116.1 mg/g under optimal conditions (initial dye concentration: 100 mg/L, contact time: 180 min, temperature: 20 °C, adsorbent dosage: 1.6 g/L, and pH: 11). FT-IR analysis indicated that electrostatic interactions and hydrogen bonding primarily govern the adsorption process. The adsorption followed pseudo-second-order kinetics and fitted well with the Langmuir isotherm model. Thermodynamic studies revealed that the adsorption was exothermic and spontaneous. A key feature of this bio hydrogel is its selective affinity for the cationic dye MB, in a mixture with Acid Orange (AO) and other cationic dyes (Rhodamine B (Rh B) and crystal violet (CV)). The adsorbent also demonstrated impressive reusability, maintaining 93 % of its efficiency after five cycles, highlighting its potential for sustainable and cost-effective water treatment.

Robust regenerable metal-selenide-chitosan photocatalyst for the effective removal of Bromothymol Blue (BB) from wastewater

Water scarcity has been a crucial debate in recent years regarding the critical scenario of water pollution. The water body is continuously contaminated by organic effluents of textile industries, including pigmented dye pollutants. To tackle water bodies contamination, there is a need to develop an eco-friendly and efficient method for removing toxic dyes. Herein, ternary metal selenide nanocomposites of barium nickel selenide (NBSe-NPs) were synthesized by the solvothermal method supported by chitosan microsphere (NBSe-NPs-CM). Recovery of the catalyst was convenient by capping nanoparticles in the microsphere to maintain effective stability, biocompatibility, and well-designed surface coating. FTIR spectrum verified nanocomposite synthesis and chitosan microsphere (NBSe-CM) formation. SEM observations of nanocomposites and NBSe-CM indicated an average size of 13.78 nm and 253 μm, respectively. The presence of barium, nickel, and selenium elements in the NBS-NPs was verified by EDX analysis. The nanocomposites had a crystallite size of 15.73 nm. The photocatalyst exhibited a narrow bandgap of only 1.3 eV based on Tauc's plot. In addition, the synthesized microsphere demonstrated an efficient photocatalytic degradation (97 %) of Bromothymol Blue dye within 100 min under optimized operating conditions (pH of 6.0, dye concentration of 40 ppm, catalyst dosage of 0.25 g). The photocatalysis process followed the pseudo-first-order kinetics. The repeatability studies showed a slight decline in the catalyst's efficiency after four successive cycles. The DFT study shows that the NBSe-CM is energetically stable with more considerable negative binding energy, and the dye molecule interacts more strongly with the NBSe-CM surface. The findings highlight the exceptional characteristics of the newly designed ternary-metal-selenide-containing chitosan-microspheres for degrading dye contaminants from textile effluents.

Garlic Peel-Based Biochar Prepared under Weak Carbonation Conditions for Efficient Removal of Methylene Blue from Wastewater

Background: Due to it containing cellulose, hemicellulose, and lignin with abundant specific functional groups which could interact with organic dyes, garlic peel (GP) might be used as an efficient biosorbent. The aim of this study is to evaluate the adsorption performances of GP-based bio-adsorbents and obtain optimum preparation conditions. Methods: GP-based bio-adsorbents were prepared by thermal pyrolysis under different temperatures (150–400 °C). The morphologies, chemical states, and surface functional groups of the adsorbents were analyzed by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). Batch experiments were conducted to investigate the adsorption of methylene blue (MB) under various conditions, including contact time, contact temperature, initial dye concentration, and initial pH value. The equilibrium adsorption data were fitted to different kinetic and isothermal models, and the adsorption thermodynamics were also calculated. Significant Findings: The physicochemical properties of the GP-based bio-adsorbents were primarily dominated by the pyrolysis temperature, because their morphologies and surface functional groups of GP-based bio-adsorbents significantly varied with the changes in pyrolysis temperature. The adsorption capacity of GP materials for MB decreased as the pyrolysis temperature increased. At an initial concentration of 50.00 mg L−1, GP150 possessed a higher adsorption capacity of 167.74 mg g−1 toward MB. The possible adsorbate–adsorbent interactions, including electrostatic attraction, hydrogen bonding, and π-π stacking, were recognized. After 10 consecutive adsorption–desorption cycles, GP150 maintained a high removal rate (88%) for MB, demonstrating its excellent adsorption performance, good reusability, and potential application in the treatment of MB-contaminated water.

Diffusion‐Free Intramolecular Triplet–Triplet Annihilation Contributes to the Enhanced Exciton Utilization in OLEDs

AbstractTriplet–triplet annihilation (TTA), or triplet fusion, is a biexcitonic process in which two triplet‐excited molecules can combine their energy to promote one into an excited singlet state. To alleviate the dependence of the TTA rate and yield on triplet diffusion in both solid and solution environments, intramolecular TTA (intra‐TTA) has been recently proposed in conjugated molecular systems able to hold multiple triplet excitons simultaneously. Developing from the previous demonstration of TTA performance enhancement in sensitized upconversion solutions, here similar improvements in triplet harvesting in solid‐state films are reported under electrical excitation in organic light emitting diodes (OLEDs). At low dye concentration and low current densities, the intra‐TTA active OLED shows a +40% improved external quantum efficiency with respect to the reference device, and a TTA spin‐statistical factor f 4DPA of 0.4, close to that determined in fluid solution for the individual chromophore (0.45). These results therefore indicate the utility of this molecular design strategy across a wider range of TTA applications, and with particular utility in the further development of low‐power TTA‐enhanced OLEDs.

Synthesis of TiO2-brookite nanorods and TiO2-Au composites for decomposition of organic dyes in water

This study employed a plasma-liquid interaction technique at room temperature to modify TiO2 nanocrystals in the brookite phase and coat their surface with gold nanoparticles (AuNPs). The technique was further utilized to reduce Au3+ ions to Au0, eliminating the need for chemical agents and reducing reaction time. The resulting TiO2-Au photocatalysts were then tested under visible light to evaluate their ability to degrade the dyes rhodamine 101 (RB101) in water. The findings indicated that the most effective degradation of RB101 molecules occurred at low dye concentrations (10 ppm) and low photocatalyst loadings with a ratio of 4. In comparing two different preparation methods, the TiO2-Au sample created using a micro-plasma process with a direct current (DC) source exhibited higher photocatalytic activity (87 % after 4 hours) compared to the sample created using a plasma jet process with an alternating current (AC) source. This research holds significance for the advancement of photocatalytic materials with potential environmental applications.

Solar driven highly efficient photocatalyst based on Dy2O3 nanorods deposited on reduced graphene oxide nanocomposite for methylene blue dye degradation.

In recent years, the demand for rare earth elements has surged due to their unique characteristics and diverse applications. This investigation focuses on utilizing the rare earth element dysprosium oxide (Dy2O3) for the photocatalytic oxidation of model pollutants under solar light irradiation. A novel RGO-Dy2O3 nanocomposite photocatalyst was developed using a solvothermal approach, Dy2O3 nanorods uniformly deposited onto reduced graphene oxide (RGO) nanosheets. Comprehensive characterization techniques, including Brunner-Emmett-Teller (BET), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FTIR), Raman spectroscopy, high resolution - transmittance electron microscopy (HR-TEM), field emission-electron scanning microscopy (FE-SEM), atomic force microscopy (AFM), electron paramagnetic resonance spectroscopy (EPR), photoluminescence spectroscopy (PL), and electrochemical impedance spectroscopy EIS techniques. The UV-visible diffusive reflectance spectroscopy (UV-Vis-DRS) studies revealed a band gap energy of 3.18eV and a specific surface area of 114 m2/g for the fabricated RGO-Dy2O3 nanocomposite. The RGO-Dy2O3 nanocomposite demonstrated a high photocatalytic degradation efficiency of 98.1% at neutral pH for methylene blue (MB) dye for the dye concentration of 10ppm. The remarkable photocatalytic performance was achieved within 60min under solar light irradiation. Reusability tests demonstrated stability, maintaining over 90% photocatalytic efficiency after three cycles. The EPR spectra and quenching experiments confirmed that photogenerated hydroxyl radicals significantly influence the photodegradation processes. The RGO-Dy2O3 nanocomposite photocatalyst, with its green, easy preparation process and recycling capabilities, presents an ideal choice for various applications. It offers a viable alternative for the photocatalytic degradation of organic dyes in real wastewater, contributing to sustainable environmental remediation.

Photoluminescence and photocatalytic activity of sol gel synthesized Mg doped TiO2 nanoparticles

The influence of magnesium doping on the optical properties, structural characteristics, and photocatalytic performance of TiO2 nanoparticles was investigated. Pure and Mg-doped TiO2 nanoparticles with varying weight percentages of magnesium were synthesized via the sol–gel method, followed by calcination at 100 °C for 12 h and annealing at 400 °C for 2 h to promote crystallization. X-ray diffraction (XRD) analyses confirmed the formation of crystalline mixed phases of anatase and rutile TiO2 nanoparticles, exhibiting their crystalline nature upon synthesis. Scanning electron microscopy (SEM) images were employed to study the morphological features of the samples, while energy dispersive spectroscopy (EDS) provided insights into their elemental composition. Photoluminescence (PL) emission spectra revealed ultraviolet (UV) to visible region emission for both pure and doped TiO2 samples. The photocatalytic activity was evaluated by monitoring the degradation of methyl orange under natural sunlight irradiation, elucidating the impact of visible light exposure. Furthermore, investigations were conducted to assess the influence of catalyst loading, initial dye concentration, and pH of the dye solution on the methyl orange removal efficiency. The 3 wt% Mg doped TiO2 exhibited 95 % of decolorization of Methyl Orange. X-ray photoelectron spectroscopy measurements was performed to verify the elemental composition and chemical valence states of each element. The scavenger test in photodegradation mechanism revealed that the main reactive species was superoxide species. The electron species resonance (ESR) measurement demonstrate that the synthesized sample shows the low spin state of Mg2+ in TiO2. The correlation between Mg doping on photocatalytic activity and crystal structure were studied. Theoretical calculations were performed to gain insights into the potential mechanism underlying the tuning of luminescent and photocatalytic properties of Mg-doped TiO2 nanoparticles, enabling a comprehensive discussion.

Bio Dyeing of Nylon 6 Fabrics Using Beetroot and Natural Mordants

AbstractIn this paper, the potential of beetroot as a natural source to dye a synthetic fiber that is, nylon 6 fabric, has been examined. We analyzed the impact of the most important dyeing parameters, such as dyeing temperature, dyeing time, pH of the dye bath, and dye concentration, on the dyeing efficiency of the nylon 6 fabric. We achieved the optimal conditions for nylon dyeing by beetroot at the boiling temperature for 60 min using 100% on the fabric weight (owf) dye under acidic conditions. Also, to attain suitable color fastness, we used four different natural mordants (pomegranate peel, walnut husk, pistachio hull, and Terminalia Chebula) before the dyeing process. We also examined the effect of four commonly used metal mordants on the dyeing efficiency. FTIR, SEM, EDX and TGA were then conducted to justify the presence of mordants and dyes on the substrate. We discovered that pre‐mordanting generated colorful fabrics based on the type of mordants used. Also, various natural mordants could produce different color strengths, such that the walnut husk had the highest color strength among the used mordants. The obtained color fastness against washing of all bio‐mordants was rated as excellent and the light fastness of Terminalia Chebula was surprisingly excellent. Bio‐mordants also exhibited equivalent washing fastness to metal mordants, even surpassing them in terms of light fastness. The EDX spectra also showed peaks corresponding to carbon (C), nitrogen (N), and oxygen (O). Finally, the fabric mordanted with pomegranate peel exhibited very less mass loss, thus indicating thermal stability.