High Dye Concentration Research Articles

Bifunctional cationic modification of modal fabric for sustainable in textile dyeing with spent coffee grounds

In order to dye cellulose or regenerated cellulose with natural dyes, toxic metal mordants are generally employed. In response to this issue, the novel bifunctional cationic agent was pretreated to modify modal (regenerated cellulose) fabric prior to dyeing to enhance the fiber-dye affinity. The cationization reaction was carried out using a compound containing bicationic sites, N,N'-(oxybis (ethane-2,1-diyl))bis(3-chloro-2-hydroxy-N,N-dimethylpropan-1-aminium. This unique cationic agent is capable of producing nonvolatile amine and has no odor problem. The successful cationic modification was confirmed through FTIR spectroscopy and zeta potential measurement. The cationized process was optimized at a cationic and sodium hydroxide concentration of 90 and 20 g∙L‒1, respectively, with a duration of 5 h. The modified modal fabric significantly enhanced its dyeability with the extract from spent coffee grounds, resulting in deep brown colors. The cationized sample's color strength was noticeably improved. Cationized samples demonstrated better color fastness to washing than untreated samples. Crock fastness was comparable, except the light fastness at high dye concentrations was slightly lower. By utilizing cationization, it offers a promising and sustainable approach enhancing the dyeing with natural dye for green textile coloration.

Comprehensive analysis of dye adsorption and supramolecular interaction between dyes and cotton fibers in non-aqueous media/less water dyeing system

Cotton textile dyeing consumes large amounts of energy and water and discharges large amount of wastewater and pollutants. Zero or less discharge of the wastewater and contaminants from the cotton textile dyeing has been under high demands from textile industry. Recently, a novel reactive dyeing technology of using a non-aqueous medium with little water (NMLW) was developed for cotton fabrics. However, the use of high concentration of reactive dyes in the system triggers aggregation of the dyes in cotton fibers, influencing the quality of dyed cotton textiles. In this investigation, adsorption, diffusion, and aggregation behavior of reactive dyes in cotton fibers were studied. Compared to traditional water-based dyeing system, cotton fabrics demonstrated superior color depth, as long with higher rates of dye uptake and fixation for reactive dyes. At low dye concentrations, the maximum absorption wavelengths of reactive dyes were unchanged, and complied with the Lambot-Beer law. However, when the dye concentration was excessively high, reactive dyes with different molecular structures, as well as multi-layer dye aggregates with π-π stacking and hydrogen bonding interactions, showed different light absorption spectral characteristics and photophysical properties. Moreover, the dye particle size and dye ionization were influenced by the dye concentration, molecular weight, molecular configuration, etc. Analysis of the molecular dynamics of reactive dyes revealed that the maximum dye aggregation size was predominantly dimer at low dye concentration. However, the dimer ratio significantly decreased, while the trimer ratio increased, and higher-order aggregates were observed at a higher dye concentration. The strength of hydrogen bonds between dye molecules and water molecules, as well as the number of water molecules surrounding dye molecules, was influenced by dye concentration and alkali. This study provides a foundation for understanding the micro-aggregation behavior of reactive dyes and offer guidance for optimizing the dyeing process in practical production settings.

Interaction between the electrochemical properties of powdered activated carbon and the biochemical processes within bacteria in Azo dye biodecolorization: An explanatory mechanism

Drawing on prior reports highlighting the redox mediator properties of powdered activated carbon (PAC), this study was designed to evaluate these properties to enhance the decolorization of azo dye by Klebsiella quasipneumoniae GT7. It was found that the presence of 0.5 % PAC in the medium increased the biodecolorization rate early in incubation. Chemical analysis revealed that dye conversion into aromatic amines occurred in microbial systems both with and without PAC. However, at initial dye concentrations (Cid) of 2 mM or higher, some dye remained on the PAC surface and in the medium. In contrast, the PAC-free system achieved nearly 100 % biodecolorization at all initial dye concentrations. The negative impact of PAC on decolorization efficiency in microbial systems with high initial dye concentrations cannot be solely explained by its redox mediator function. This study used the amphoteric-Donnan model for PAC's electrical double layer (EDL) and Mitchell's chemiosmotic model for bacterial proton motive force (PMF) to explore this. It found that charge storage in PAC's EDL regulates electron transfer fluxes, and proton species enhance the proton motive force across the bacterial membrane. These observations improve the understanding of PAC's role in microbial decolorization and its potential future applications.

Electrochemical treatment on a pilot scale of a mixture with high concentrations of dyes from the tanning/textile industry

Violet LR (VLR), Brown RD (BRD), and Green A (GA) dyes are widely used in the tannery industry for dyeing leather. These types of compounds can be toxic and, in many cases, carcinogenic. In this context, electrochemical oxidation (EO) and electro-Fenton (EF) processes are the most popular electrochemical advanced oxidation processes (EAOPs) to degrade persistent/toxic water pollutants. The efficiency of these processes largely depends on the nature of the electrode materials, among other operation parameters. This study evaluates Ti/IrO2-SnO2-Sb2O and BDD anodes for dye degradation in a pilot plant of 4.0 L of total volume. It was found that DSA IrO2-SnO2-Sb2O performed better than BDD for the discoloration of a mixture of the dyes (kDSA=0.0970 min−1 and kBDD=0.0370 min−1) in a medium containing 50 mM NaCl and 10 mM Na2SO4 (j = 50 mA cm−2, Q=12 L min−1 and pH 3). Such an effect was due to the combined production of heterogeneous •OH at the anode surface by H2O oxidation and reactive chlorinated species in the bulk solution via Cl- oxidation. In addition, •OH quantification showed a higher production by DSA ([BDD(•OH)] = 3,8 × 10-15 M vs [DSA(•OH)] = 6.6 × 10-15 M). The efficiency was enhanced when applying EF (BDD cathode promoting H2O2 production) in the presence of Fe2+ ions under similar experimental conditions. The color was almost totally removed in 50 min with kEF-DSA=0.1584 min−1, while COD was removed by 80 % in 80 min. The EC was 0.082 kWh (g COD)-1. Such results highlight the potential of EO and EF with accessible Ti/IrO2-SnO2-Sb2O anodes as a pretreatment unit within a treatment train for tanning or textile wastewater management.

Efficient removal of high concentration dyes from water by functionalized in-situ N-doped porous biochar derived from waste antibiotic fermentation residue

Using biochar for dye wastewater treatment is attracting interest due to its excellent adsorption properties and low costs. In this work, a novel biochar derived from oxytetracycline fermentation residue (functionalized OFR biochar, FOBC) was investigated as a efficient adsorbent for typical dyes removal. At 25 °C, the maximum adsorption capacity calculated by Langmuir model of FOBC-3-600 for methylene blue (MB), malachite green (MG), and methyl orange (MO) reached 643.97, 617.89, and 521.03 mg/g, respectively. The kinetics and isotherm model fitting showed that the chemisorption and physisorption both occurred during the adsorption process. Dyes were efficiently adsorbed through pore filling, electrostatic attraction, π-π interactions, and surface complexation. And the cycling experiment and environmental risk assessment indicated that the FOBC-3-600 had excellent recyclability and utilization safety. Overall, this study provides a practical method to simultaneously treat the dyeing wastewater and utilize the antibiotic fermentation residue.

Study on Methylene Blue Adsorption Properties of Biochar/Montmorillonite Composites

The textile printing and dyeing industry, as one of the important pillars of the global economy, has become an environmental problem that needs to be solved because of the increasingly serious pollution of dye wastewater generated during its production process. Dye wastewater not only contains high concentrations of organic dyes, but also often accompanied by heavy metal ions, additives and salts and other pollutants, if discharged directly without effective treatment, will seriously pollute the water body, destroying the ecological balance, and affecting the survival and health of human beings and aquatic organisms. In order to deal with the problems of serious pollution, large discharge and high cost of dye wastewater, it is necessary to develop an efficient, economic and environmentally friendly wastewater treatment system. It is particularly important to develop efficient, economical and environmentally friendly wastewater treatment technologies. Adsorption is considered as a promising method for wastewater treatment. In this study, we focused on the development of new and efficient adsorbent materials. Taking methylene blue, a typical dye, as an example, we skillfully composited modified biochar with montmorillonite, a natural mineral material, through pyrolysis and intercalation strategies, and conducted in-depth investigations on the effects of the composites on the adsorption of methylene blue in water, the factors affecting the regeneration performance of the adsorbents, and the thermodynamic characteristics of the adsorption. The effect of the composite material on the adsorption of methylene blue in water, the factors affecting the regeneration performance of the adsorbent and the adsorption thermodynamic characteristics were investigated in depth, with a view to providing certain theoretical and practical references for the effective treatment of dye wastewater.

Biodegradable Acid-Based Fe2MnO4 Nanoparticles for Water Remediation.

This study demonstrated the synthesis of Fe2MnO4 modified by citric acid, a biodegradable acid, using a simple co-precipitation method. Characterization was performed using qualitative analysis techniques such as Fourier-transformed infrared spectroscopy, scanning electron microscopy equipped with energy-dispersive X-ray spectroscopy, X-ray diffraction, selected-area electron diffraction, N2 adsorption-desorption, and zero-point charge. The prepared nanoparticles had a rough and porous surface, and contained oxygenous (-OH, -COOH, etc.) functional groups. The specific surface area and average pore size distribution were 83 m2/g and 5.17 nm, respectively. Net zero charge on the surface of the prepared nanoparticles was observed at pH 7.5. The prepared nanoparticles were used as an adsorbent to remove methylene blue dye from water under various conditions. Using small amounts of the adsorbent (2.0 g/L), even a high concentration of MB dye (60 mg/L) could be reduced by about ~58%. Exothermic, spontaneous, feasible, and monolayer adsorption was identified based on thermodynamics and isotherm analysis. Reusability testing verified the stability of the adsorbent and found that the reused adsorbent performed well for up to three thermal cycles. Comparative analysis revealed that the modified adsorbent outperformed previously reported adsorbents and unmodified Fe2MnO4 in terms of its partition coefficient and equilibrium adsorption capacity under different experimental conditions.

Small-Molecule:Polymer Composites for Transparent Films with Visible Emission.

The analysis of the shift in photoluminescence emission for a blend of polyvinylcarbazole and acrylonitrile derivative compounds is reported. The small-molecule compounds have different functional groups, phenyl, pyridine, or methyl phenyl, attached to an acrylonitrile group. According to the functional group, the blue emission for pure dye shifts to green or yellowish in the blend film. Several PVK:dye ratios from 0:100 to 20:80 were used for film deposition. The film morphology was analyzed by atomic force microscopy; for low dye content, homogeneous films were achieved. However, aggregates of several micrometers are formed on the surface of films with higher dye concentrations. The shift in emission occurs only with PVK, and for a non-conjugated matrix such as polystyrene, the emission remains unchanged. The interaction of dyes with PVK leading to change in emission was also achieved by grinding dye and polymer. Results showed that shifts in emission could come from exciplex formation along with changes in dye intermolecular interactions. The blend films were highly transparent in the visible spectra due to the absorption in the UV region for dye and matrix. The films with ratio PVK: dye ratio 80:20 was used as active layer in OLEDs.

The development of Giant reed biochar for adsorption of Basic Blue 41 and Eriochrome Black T. azo dyes from wastewater

The textile industry is discharging high concentrations of anionic and cationic azo dyes into the nearby environment, which can cause adverse effects on public health, and the aquatic environment. Therefore, this study aimed to develop giant reed biochar and apply for the removal of Basic blue 41 (BB41) and Eriochrome black T (EBT) azo dyes from water. Characterization techniques such as BET surface area analyzer, Fourier-transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and thermal gravimetric analyzer (TGA) were applied for biochar description. The biochar exhibits a high fixed carbon content (80.4%), a low ash content (3.8%), a large surface area (429.0 m2/g), and good thermal stability. High removal efficiencies of BB41 98.6% and EBT 82.5% were recorded at the specific experimental condition. The experimental data were fitted with the Langmuir isotherm model at R2 0.99 for both dyes whereas the adsorption kinetics revealed the pseudo-second-order kinetics at R2∼\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\sim$$\\end{document} 1 and 0.99 for BB41 and EBT, respectively. Furthermore, four regenerations of biochar with adsorption performances of BB41 and EBT dyes were found to be 94.7% and 79.1%, respectively. Finally, this adsorbent can be considered an economically viable material for the removal of synthetic dyes from wastewater systems. In conclusion, the study findings showed that the adsorbent material is promising to apply for water and wastewater treatment but still, the study of adsorption interaction and modifications of the surface functionalities are essential to accommodate multipollutant removal from real water systems.

Efficient removal of direct dyes by SA-Er biopolymer gel spheres: Equilibrium isotherms, kinetics and regeneration performance study

Biomass-based adsorbent materials are characterized by their low cost, environmental friendliness, and ease of design and operation. In this study, biomass-based hydrogel microspheres erbium alginate (SA/Er) with high stability and adsorption properties were prepared by a one-step synthesis method. The prepared materials were characterized and analyzed by SEM-EDS, XRD, TGA, FT-IR, UV–Vis, BET-BJH and XPS, and the adsorption performance of SA/Er was investigated for high concentrations of azo dyes in water. The results showed that the adsorption performance of SA/Er on the azo dyes of direct violet N (DV 1) and direct dark green NB (DG 6) with concentrations of 850 mg/L and 1100 mg/L under the optimal conditions was very high, and the adsorption amount could be up to 692 mg/g and 864 mg/g, respectively. The adsorption process was in accordance with the quasi-secondary kinetic model, which was accomplished by physical and chemical adsorption; the Langmuir isothermal model was able to better respond to the adsorption equilibrium, and the adsorption was dominated by the adsorption of surface monolayers; after seven desorption cycles, the removal of both azo dyes by the adsorbent material could reach >79.7 %. Combined with the results of FT-IR, UV–vis and XPS analysis before and after the adsorption, it was revealed that the adsorption of SA/Er with the dye molecules mainly consisted of hydrogen bonding, electrostatic adsorption and surface complexation, which resulted in the significant adsorption effect on the two azo dyes, and the above results can provide a reference for the treatment of dye wastewater.

Establishment of a rapid, cost-effective, and accurate method for assessing insect sperm viability

High-quality sperm cells are crucial to reproductive success for both males and post-mating females in animals. Sperm viability, defined as the proportion of viable sperm cells, is used as a sperm quality index and this method has provided new insights into research on reproductive strategies. Sperm viability has been assessed by fluorescent staining of sperm cells. However, current staining protocols could potentially underestimate viability due to cell damage caused by cell treatments such as high dye concentration and long time for post-mounting. In this study, we established a method that enables rapid sperm viability assessment, has low sperm cell toxicity, and provides precise results regardless of operator expertise, and cost-effective using sperm cells from an ant, Crematogaster osakensis (Hymenoptera). First, to shorten the time for observation of a sufficient number of sperm cells, the volume per field of view was increased by height elevation between the glass slide and the coverslip, thereby we increased the number of sperm cells in a field of view. Second, to reduce sperm cell toxicity, we optimized the minimum dye concentration and incubation time using acridine orange (AO) and Hoechst in addition to SYBR 14 and propidium iodide (PI), which has been used in most previous studies. We determined the optimal protocol to be 1 µg/mL AO and 150 µM PI without incubation. Besides, we automated counting sperm cells with ImageJ software and combined with manual correction for more accurate results. We employed the improved method for sperm samples from mealworm beetles (Tenebrio molitor) and silkmoths (Bombyx mori). This method, established through our study, will advance research on reproductive strategies, including sperm competition and sperm quality maintenance in females.

Film Temperature And Thickness Measurements Of An Impinging Oil Jet For Cooling Of Electric Components Based On Two-Color Laser-Induced Fluorescence.

A fluorescence based two-color detection scheme is used to characterize a jet impingement cooling process relevant for electric and electronic applications. The presented technique enables a simultaneous determination of film temperature and film thickness. The fluorescence signal was generated by the temperature-sensitive fluorescence tracer nile red, which was added to Marlotherm LH, a commercially available heat transfer oil. Suitable band pass filters enable accurate temperature measurements. A preliminary spectral study investigates the influence of dye concentration, temperature and film thickness. At high dye concentrations (up to 37.5 mg/L) reabsorption effects takes place and lead to a spectral shift towards higher wavelengths with increasing film thickness. Low dye concentrations (0.59 mg/L) exhibit no film thickness dependent spectral shift. A film temperature investigation at low dye concentration showed no bias of the intensity ratio due to film thickness, i.e. no additional spectral shift towards lower wavelengths was observed. The investigations on the jet impingement setup revealed an increasing film temperature and decreasing film thickness with increasing solid temperature. The average film temperature increases with increasing solid temperature from 298 K (solid temperature 298 K) to 308 K (solid temperature 398 K). At higher solid temperatures, the film temperature increases with distance to the stagnation zone. The average film thickness decreases with increasing solid temperature from 0.24 mm to 0.17 mm. At high solid temperatures, the film temperature increased with radial distance to the stagnation zone. This behavior is caused by the increasing temperature gradient with increasing solid temperature and decreasing viscosity with increasing film temperature.

Fluorescence Lifetime Measurement For Studying Evaporation Of Bi-Component Droplet

Sprays are essential in engineering applications like evaporators and combustion chambers. Predicting the evaporation of multi-component liquid droplets is complex due to changing composition and properties. Measuring droplet composition is challenging, with limited non-intrusive methods available. Raman spectroscopy faces hurdles like weak signals and interference. Intensity based Laser-Induced Fluorescence (LIF) requires optical models to interpret data due to varying droplet size and position. Fluorescent dyes in liquid mixtures are sensitive to temperature, complicating measurements. Fluorescence lifetime measurements offer a promising alternative, being an absolute quantity less affected by reabsorption. This study develops a novel method using fluorescence lifetime to analyze droplet composition, leveraging Time-Correlated Single Photon Counting (TCSPC) for precise measurements. Factors such as dye concentration, solvent polarity, and temperature sensitivity are investigated. Calibration curves for ethanol-water mixtures correlate fluorescence lifetime with volume fraction. Experimental setups use TCSPC and femtosecond lasers for dye excitation. Results show that fluorescence lifetime decreases linearly with solvent polarity and is influenced by temperature and dye concentration. High dye concentrations cause self-quenching, altering temperature sensitivity. The method was applied to study the evaporation of ethanol-water droplets under acoustic levitation. Findings indicate that evaporation rates slow as the water fraction increases, with initial measurements showing higher water content due to partial evaporation. This research introduces a novel technique for droplet compositional analysis using fluorescence lifetime, providing insights into optimizing measurement accuracy and advancing understanding in engineering and related fields.

Sodium lignosulfonate as an extracting agent of methylene blue dye using a polymer-enhanced ultrafiltration technique

The purpose of this research was to evaluate the efficacy of sodium lignosulfonate (LS) as a dye adsorbent in the removal of methylene blue (MB) from water by polymer-enhanced ultrafiltration. Various parameters were evaluated, such as membrane molecular weight cut-off, pH, LS dose, MB concentration, applied pressure, and the effect of interfering ions. The results showed that the use of LS generated a significant increase in MB removal, reaching an elimination of up to 98.0 % with 50.0 mg LS and 100 mg L−1 MB. The maximum MB removal capacity was 21 g g−1 using the enrichment method. In addition, LS was reusable for up to four consecutive cycles of dye removal-elution. The removal test in a simulated liquid industrial waste from the textile industry was also effective, with a MB removal of 97.2 %. These findings indicate that LS is highly effective in removing high concentrations of MB dye, suggesting new prospects for its application in water treatment processes.

Visualizing preferential flow paths using dye tracer and species diversity theory methods to explore their correlation to soil properties with random forest algorithm

The preferential flow path development is potentially the result of spatial variations in soil properties with soil depth. However, visualizing the evolution of the preferential flow path with soil depth remains a challenge. This paper presents dye tracer and species diversity theory methods for characterizing preferential flow paths. Field dye tracer experiments were performed at three sites (tree, bush, and grass) in the Yellow River Delta wetland and dye distribution diversity indices (Simpson index (Ds), Shannon-Wiener index (H), Margalef index (Dm), and Pielou index (E)) were applied to verify their availability for preferential flow assessment. The results showed that the uniformity of the shallow-infiltrated dye at the tree site, non-uniformity of the shallow-infiltrated dye at the bush site, and deep dye infiltration at the grass site were the three typical infiltration types. The average proportion of dye-stained areas (PDA) gradually decreased with increasing soil depth. The quantitative effects of soil properties on PDA changes were profound, indicating that soil clay content at 0–10 cm depth, soil sand content at 10–20 cm depth, soil drainage capacity at 20–30 cm depth, and soil bulk density at 30–40 cm depth were the most predictive factors controlling PDA changes. Our results also showed that dye-stained patches with extremely high and high dye concentrations were the most distributed; Ds, H, Dm, and E were the highest at the tree site and E was the diversity index with the greatest importance for PDA change. The findings reveal the soil properties controlling the formation of preferential flow paths, which will improve our understanding of water resource management in the vadose zones of coastal wetlands.

Peroxymonosulfate activation by iron-cobalt bimetallic phosphide modified nickel foam for efficient dye degradation

Novel catalysts with multiple active sites and rapid separation are required to effectively activate peroxymonosulfate (PMS) for the removal of organic pollutants from water. Therefore, an integrated catalyst for PMS activation was developed by directly forming Co–Fe Prussian blue analogs on a three-dimensional porous nickel foam (NF), which were subsequently phosphorylated to obtain cobalt-iron bimetallic phosphide (FeCoP@NF). The FeCoP@NF/PMS system efficiently degraded dye wastewater within 20 min. The system exhibited excellent catalytic degradation over a broad pH range and at high dye concentrations due to the presence of unique asymmetrically charged Coa+ and Pb− dual active sites formed by cobalt phosphides within FeCoP@NF. These active sites significantly enhanced the catalytic activity of PMS. The activation mechanism of PMS involves phosphorylation that accelerates electron transfer from FeCoP@NF to PMS, to generate SO4·–, ·OH, O2·–, and 1O2 active species. Three-dimensional FeCoP@NF could be readily recycled and showed good stability for PMS activation. In this study, a highly efficient, stable, and readily recyclable integrated catalyst was developed. This catalyst system effectively resolves the separation and recovery issues associated with conventional powder catalysts and has a wide range of potential applications in wastewater treatment.

Reviewing the effect of aggregates in Rhodamine 6G aqueous solution on fluorescence quantum efficiency

Rhodamines constitute a class of dyes extensively investigated and applied in various contexts, primarily attributed to their high luminescence quantum yield. This study delves into the impact of aggregation on the thermal and optical properties of Rhodamine 6G (R-6G) solutions in distilled water. Examined properties encompass thermal diffusivity (D), temperature coefficient of the refractive index (dn/dT), fluorescence quantum efficiency (η), and energy transfer (ET). These parameters were assessed through thermal lens (TL) and conventional absorption and emission spectroscopic techniques. The dimerization of R-6G solutions was revisited, revealing that an increase in R-6G concentration alters the features of absorption and emission spectra due to dimer formation, resulting in unexpected behavior of η. Consequently, we introduce a novel model for the fraction of absorbed energy converted into heat (φ), which accounts for emissions from both monomers and dimers. Employing this model, we investigate and discuss the concentration-dependent behaviors of η for monomers (ηm) and dimers (ηd). Notably, our findings demonstrate that ηm values necessitate ηd = 0.2, a relatively substantial value that cannot be disregarded. Additionally, applying the Förster theory for dipole–dipole electric ET, we calculate microparameters for ET between monomers (CDD) and monomer–dimer (CDA). Critical ranges for ET in each case are quantified. Microparameter analysis indicates that ET between monomer–monomer and monomer–dimer species of R-6G dissolved in distilled water holds significance, particularly in determining ηm. These results bear significance, especially in scenarios involving high dye concentrations. While applicable to R-6G in water, similar assessments in other media featuring aggregates are encouraged.

Preparation of Flower-like Nanosilver Based on Bioderived Caffeic Acid for Raman Enhancement and Dye Degradation.

In this study, a simple, green, and low-cost room temperature synthesis of broccoli-like silver nanoflowers (AgNF) with a particle size of about 300-500 nm was developed using plant-derived caffeic acid as a reducing agent and polyvinylpyrrolidone as a dispersant under ultrasound assistance. The flower clusters covered by small nanocrystals of 20-50 nm significantly enhance the electromagnetic field signals. AgNF was deposited on the surface of silicon wafers as a surface-enhanced Raman spectroscopy sensor for the detection of probe molecules such as rhodamine 6G (R6G) and malachite green with high sensitivity, homogeneity, and reproducibility. AgNF was deposited on cotton fabrics in the form of composites to catalyze the degradation of dye pollutants such as R6G, MG, and methyl orange in the presence of sodium borohydride. 0.1 g of AgNF/cotton fabric could assist 15 mmol/L NaBH4 to achieve over 90% degradation of various dyes as well as a high concentration of dyes in 12 min with good reusability and recyclability. The AgNF synthesized in this work can not only monitor the type and amounts of pollutants (dyes) in wastewater but also catalyze the rapid degradation of dyes, which is expected to be valuable for industrial applications.

Simultaneous film temperature and film thickness measurements for jet impingement applications using two-color laser-induced fluorescence

The study investigates a jet impingement cooling process of a cylindrical geometry relevant for electric and electronic applications. The applied two-color detection technique enables a simultaneous determination of film temperature and film thickness. For this purpose, the heat transfer oil Marlotherm LH was doped with the temperature-sensitive fluorescence tracer nile red. The temperature determination was realized by suitable band pass filters. Preliminary spectral investigations were carried out in terms of varying dye concentration, temperature and film thickness. At high dye concentrations (up to 37.5 mg/L), reabsorption effects lead to a spectral shift toward higher wavelengths with increasing film thickness. Low dye concentrations (0.29 mg/L, 0.59 mg/L) show no film thickness dependent spectral shift. A film temperature investigation at low dye concentration showed no bias of the intensity ratio due to film thickness, i.e., no additional spectral shift toward lower wavelengths was observed. The investigations on the jet impingement setup revealed an increasing film temperature and decreasing film thickness with increasing solid temperature. The average film temperature increases with increasing solid temperature from 298 (solid temperature 298 K) to 308 K (solid temperature 398 K). At higher solid temperatures, the film temperature increases with distance to the stagnation zone. The average film thickness decreases with increasing solid temperature from 0.24 to 0.17 mm. At high solid temperatures, the film temperature increased with radial distance to the stagnation zone. This behavior is caused by the increasing temperature gradient with increasing solid temperature and decreasing viscosity with increasing film temperature.

An excellent photodegradation efficiency of methylene blue and rhodamine B dyes in a series of porphyrinic Aluminum-based MOFs metallated by copper and cobalt metals

A series of Al-porphyrin-based MOF materials have been fabricated through the solvothermal route, denoted as AlPMOF(M). In particular, the AlPMOF(M) materials adopt the unique photoabsorption property in visible light regions, which can effectively degrade organic dyes from wastewater. Noteworthily, Cu-metallated AlPMOF displays an extraordinary photodegradation activity of organic pollutants with a high efficiency of 98% for methylene blue and 96% for rhodamine B after 300 min upon irradiation of visible light at a high initial dye concentration (100 mg L−1). Additionally, each AlPMOF(M) retains the photodegradation efficiency of methylene blue and rhodamine B for at least seven cycles without any considerable decrease in performance. Interestingly, the intermediate products of the photocatalytic decomposition process were interpreted through an ultra-performance liquid chromatography-mass spectrometry procedure. These results prove that AlPMOF(Cu) could be a promising photocatalytic material to remove highly toxic organic contaminants from wastewater.