Commercial Dyes Research Articles

Organic doped red room-temperature afterglow materials based on 2,3,5-triarylfuro[3,2-b]pyridines through Förster-resonance energy transfer

A series of novel 2,3,5-triarylfuro[3,2-b]pyridines are designed and acquired to be used as the guest molecules in organic doped room-temperature phosphorescence (RTP) system. Phenyl(pyridin-2-yl)methanone which can provide the rigid and tight microenvironment is chosen as the host molecule, which enables the two-component doped materials to emit RTP emissions of 0.5–8 s with 41–565 ms phosphorescence lifetimes and 2.9–19.4 % phosphorescence quantum efficiencies through constricting the non-radiative decay of triplet excitons. Furthermore, using commercial dyes Erythrosin B sodium salt and Eosin Y sodium salt as the third component and energy acceptor, the three-component materials emit bright red afterglows of 2 s with delayed lifetimes of 252–286 ms and emission quantum yields of 5.1–5.6 %, which are demonstrated to come from the triplet-to-singlet Förster-resonance energy transfer (FRET) from phosphorescence emission of 2,3,5-triarylfuro[3,2-b]pyridine derivative to fluorescence emission of commercial dye. This work not only provides valuable reference for the development of furo[3,2-b]pyridine-based afterglow materials, but also proves that the strategy of the FRET process provides new possibilities for molecules that can only emit fluorescence to participate in constructing afterglow materials.

Microwave-Assisted Hydrothermal Synthesis of Photocatalytic Truncated-Bipyramidal TiO2/Ti3CN Heterostructures Derived from Ti3CN MXene.

TiO2/MXene heterostructure has garnered significant interest as a photocatalyst due to its large surface area and efficient charge carrier separation at the interface. However, current synthesis methods produce TiO2 without clear crystal faceting and often require complicated postprocessing step, limiting its practical applications. We demonstrate a facile and controlled microwave-assisted hydrothermal synthesis for transforming multilayered Ti3CN MXene to a truncated-bipyramidal TiO2/Ti3CN heterostructure. The resulting TiO2 nanocrystals at the Ti3CN surface exhibited crystalline anatase truncated bipyramids, exposing {001} and {101} facets. We further tailored an indirect optical band gap of the TiO2/Ti3CN heterostructure in the range of 3.17-3.23 eV by varying the hydrothermal synthesis time from 15 min to 5 h at a fixed temperature of 160 °C. Efficient charge separation allowed us to decompose 97% of methylene blue (MB) within 30 min of ultraviolet (UV) light irradiation, ∼3.9-fold faster than the benchmark P25, higher than any other TiO2/MXene heterostructures. With simulated white light, we achieved over 60% efficiency of the dye decomposition within 2 h of irradiation, which resulted in 1.5-fold faster kinetics than P25. We also observed a similar excellent performance of Ti3CN-derived TiO2 in decomposing various persistent synthetic dyes, including commercial textile dye, methyl orange, and rhodamine B. In conclusion, our study provides a strategy for utilizing MXene chemical reactivity to produce highly crystalline optically active TiO2/Ti3CN heterostructure. The developed heterostructure can serve as an efficient photocatalyst for the degradation of organic pollutants.

Characterization of food color additives and evaluation of their acute toxicity in Wistar albino rats

Background and Aim: The use of food dyes can cause certain diseases, such as anemia and indigestion, along with other disorders, tumors, and even cancer. Therefore, this study aimed to determine the chemical nature and toxicity of some commercial dyes locally used in processed foods compared with standard food dyes. Materials and Methods: Three types of standard and commercial food color additives (Sunset Yellow, Tartrazine, and Carmoisine) were extensively examined. The chemical structures and functional groups of the dyes were evaluated by Fourier-transform infrared (FTIR) spectroscopy. The melting temperatures of the dyes were also determined by chemical thermal analysis. The acute toxicity test to evaluate the standard and commercial food color safety was estimated by a range-finding study using 150 Wistar albino rats. Sub-groups were administered one of the three colors under study at doses of 2, 3, 4, and 5 g/kg body weight (BW) orally for 7 days. When no mortality was observed, an additional 15 g/kg BW was administered. Concerning the median lethal dose 50 (LD50), 38 rats were exploited using the up-and-down method. Results: Commercial dyes had lower melting points than standard colors. Regarding the range-finding study, rats receiving different doses of the dyes exhibited no signs of toxicity, no deaths, and no clinical or gross pathological signs throughout the 7 days of the experiment. However, the animals that were dosed with 15 g/kg BW of each dye showed signs of loss of appetite, tachycardia, drowsiness, and eventual death. The LD50 values of the commercial food dyes, particularly Sunset Yellow and Carmoisine, were lower than those of the standard dyes. Conclusion: Commercial food colors were more toxic to rats than standard food colors. Differences were observed between the purity of the standard and commercial dyes, and the latter ones contained different percentages of salt, indicating the occurrence of fraud in commercial markets. Keywords: acute toxicity, food colors, Fourier-transform infrared spectroscopy, lethal dose 50, range-finding study.

A novel fluorescent probe for viscosity and polarity detection in real tobacco root cells and biological imaging.

The disruption of lipid droplet function is associated with the pathogenesis of various diseases. Clarifying the response behavior of lipid droplets to the microenvironment at the cellular level is of great significance. Plant lipids not only exist in phospholipids in cell membranes, but also in aromatic essential oils. Monitoring the level of lipid droplets in plant cells using fluorescent probes provides a simple method for screening lipid-rich varieties. We synthesized a polarity-viscosity responsive coumarin fluorescent probe, Cou-CN, which achieved sensitive detection of polarity and viscosity in dilute solution environments by constructing this simple probe with ICT and TICT properties and verifying it using Gaussian computational simulation. Cou-CN exhibited good lipid droplet illumination effects in HepG2 cells with a correlation coefficient of 0.92 compared to the commercial lipid droplet dye BODIPY. Additionally, co-staining the probe with the lipophilic commercial dye Nile Red in tobacco root stem seedling cells resulted in a high correlation coefficient of 0.9.

HYDROTHERMAL SYNTHESIS OF NITROGEN-DOPED CQDS OF RUBUS NIVEUS LEAVES FOR FLUORESCENT pH SENSING AND PHOTOCATALYTIC APPLICATIONS

The development of a fluorescent pH sensor and the treatment of wastewater with nanoparticles are both critical topics. The variation in pH impacts the morphology and subsequent properties of the nanoparticles, which are used for their utilization in various fields and the second one gives a better treatment approach for industrial waste entities. The present study examines the effects of these variables on the biologically produced nitrogen-doped carbon quantum dots (NCQDs). Hydrothermal process was performed for the synthesis of the same by using Rubus-niveus leaf extract as a precursor. The UV-Vis spectroscopy analysis shows absorption spectra in the wide range of 200 nm to 800 nm and shows prominent peaks at 236 nm and 392 nm, respectively. Further, the direct energy band gap of 3.65eV was analysed for NCQDs. The SEM image shows flower-shaped particles, and FT-IR analysis indicates the existence of amide, CHO, N-H, and C-N functional groups. XRD pattern showed that the surface morphology of NCQDs is amorphous in nature. A good response was found in the variation of fluorescence intensity with the pH values, confirming the possibility of NCQDs serving as pH sensors. Rhodamine-B (Rh-B) dye's reaction kinetics was revealed for the purpose of analyzing the potential of NCQDs for the degradation of commercial dyes and found to be followed by pseudo-first order kinetics with the correlation coefficient of 0.80.

Dyeing waters: Does indiscriminate dye use threaten aquatic ecosystems?

Aquatic ecosystem conservation is imperative to reaching global biodiversity and sustainability targets. However, the ecological status of waters has been continuously eroded through mismanagement in the face of existing and emerging anthropogenic stressors, such as pollutants. There has been an emerging trend towards the use of dyes to manage algae and plants as well as to alter aesthetics within various aquatic environments. This artificial colouring has potential ecological implications through reductions in light levels and disruptions to thermoclines (i.e., temperature regime changes with depth). Abiotic regime shifts could in turn drive ecological cascades by depowering primary production, hampering top-down trophic interactions, and affecting evolved animal behaviours. Despite commercial dyes being marketed as acutely non-toxic, very little is known about the chronic effects of these dyes across ecological scales and contexts. We thus call for greater research efforts to understand the ecological consequences of dye usage in aquatic environments, as well as the socio-cultural drivers for its application. This emerging research area could harness approaches such as biological assays, community module experiments, remote sensing, culturomics, and social surveys to elucidate dye effects, trends, and perspectives under a pollution framework. A greater understanding of the potential effects of dye in aquatic ecosystems under relevant contexts would help to inform management decisions and regulation options, while helping to mediate ecocentric and anthropocentric perspectives.

Properties of hydrogel for adsorbent textile dye waste based cellulose-carboxymethyl sago starch

Abstract The use of a single natural polymer in hydrogel preparations is considered insufficient to produce hydrogels that are more durable, more stable, and stronger. Blends of various natural polymers can improve each sago other’s lack of physicochemical characteristics and produce new properties. This research combines two natural polymers, cellulose and starch. Cellulose isolation from Gracilaria verrucosa seaweed using acid hydrolysis and alkaline autoclaving method produced 14.01% cellulose. This study combined the results of cellulose isolation with carboxymethyl sago starch at 0.09; 0.14 and 0.24 mol/mol AGU. The isolated cellulose-carboxymethyl sago starch has the potential as a hydrogel material with the addition of crosslinkers such as epichlorohydrin (ECH). This study aims to synthesize hydrogels from cellulose-carboxymethyl sago starch with application as a textile dye waste absorbent with a concentration of epichlorohydrin (ECH) at 7.5%. Analysis of carboxymethyl sago starch is degrees of substitution, water-soluble index (WSI), and swelling power (SP). The hydrogel properties are characterized by the degree of swelling, degree of polymerization, FTIR, and SEM, and the hydrogel adsorption ability is characterized by adsorption efficiency using a microplate reader. The research results show that hydrogel can be synthesized optimally by adding carboxymethyl sago starch (CMSS) at 0.24 mol/mol AGU. The results of FTIR analysis are also by chemical measurements (swelling and gel fraction). In contrast, for maximum colour absorption, the addition of carboxymethyl sago starch is 0.09 mol/mol AGU for purple, yellow, and black and 0.14 mol/mol AGU for green color absorption. In conclusion, the adsorption ability of hydrogel in commercial textile dyes is maximum when the carboxymethyl sago starch (CMSS) is added at 0.09 mol/mol AGU with the best adsorption efficiency at purple 86.22%, yellow 77.40%, black 73.70% and at the addition of CMSS 0.14 mol/mol AGU the best adsorption efficiency in green is 73.46%.

A Hydrogen Bonded Non-Porous Organic-Inorganic Framework for Measuring Cysteine in Blood Plasma and Endogenous Cancer Cell.

An imbalance in cysteine (Cys) levels in the cells and plasma has been identified as the risk indicator for various human diseases. The structural similarity of cysteine with its congener homocysteine and glutathione offers challenges in its measurement. Herein, we report a hydrogen-bonded organic-inorganic framework of Cu(II) (HOIF) for the selective detection of cysteine over other biothiols. The non-fluorescent HOIF showed 12-fold green emission in the presence of cysteine. The monomeric unit of HOIF is stabilized via intermolecular hydrogen bonds, resulting in a non-porous network structure. Non-interference from homocysteine, glutathione, and other competitive bio-analytes revealed explicit affinity of HOIF for cysteine. Fluorimetric titration showed a wide working concentration window (650 nM-800 μM) for measuring cysteine in an aqueous medium. The mechanistic investigation involving HRMS, EPR, and UV-vis spectroscopic studies revealed the decomplexation of HOIF with Cys, resulting in a fluorescence turn-on response from the luminescent ligand. Validation using a commercial dye, "Cysteine Green", confirmed the prospect of HOIF for early diagnostic purposes. Utilizing the fluorescence turn-on property of HOIF in the presence of cysteine, we measured cysteine quantitatively in the blood plasma samples. Bio-imaging of endogenous cysteine in cancer cells indicated the ability of HOIF to monitor the intracellular cysteine.

Synthesis and optical properties of tyramine-functionalized boron dipyrromethene dyes for cell bioimaging

Tyramine signaling amplification (TSA) technology is generally applied in immunofluorescence, enzyme-linked immunoassays, in situ hybridization techniques, etc. Successful amplification of fluoresence signals cannot be achieved without excellent fluorescent dyes. BODIPY fluorophore is an ideal probe for cell fluorescence imaging, but pristine BODIPY cannot be direct used in the TSA system. In the paper, the new red-shifted tyramide-conjugated BODIPY (BDP-B/C/D) was synthesized via the Knoevenagel condensation reaction, which based on the tyramide-conjugated BODIPY (BDP-A). The synthesized dyes were combined with tyramine to obtain which could be used as a fluorescent substrate for enzymatic reaction of TSA. By using the selected substrate (BDP-C) in TSA, we found it to be more sensitive than the commercial dye 594 styramide for the detection of low-abundance antigen proteins.

Combatting synthetic dye toxicity through exploring the potential of lignin peroxidase from Pseudomonas fluorescence LiP RL5.

Untreated release of toxic synthetic and colorful dyes is a serious threat to the environment. Every year, several thousand gallons of dyes are being disposed into the water resources without any sustainable detoxification. The accumulation of hazardous dyes in the environment poses a severe threat to the human health, flora, fauna, and microflora. Therefore, in the present study, a lignin peroxidase enzyme from Pseudomonas fluorescence LiP-RL5 has been employed for the maximal detoxification of selected commercially used dyes. The enzyme production from the microorganism was enhanced ~ 20 folds using statistical optimization tool,response surface methodology. Four different combinations (pH, production time, seed age, and inoculum size) were found to be crucial for the higher production of LiP. The crude enzyme showed decolorization action on commonly used commercial dyes such as Crystal violet, Congo red, Malachite green, and Coomassie brilliant blue. Successful toxicity mitigation of these dyes culminated in the improved seed germination in three plant species, Vigna radiate (20-60%), Cicer arietinum (20-40%), and Phaseolus vulgaris (10-25%). The LiP treated dyes also exhibit reduced bactericidal effects against four common resident microbial species, Escherichia coli (2-10mm), Bacillus sp. (4-8mm), Pseudomonas sp. (2-8mm), and Lactobacillus sp. (2-10mm). Therefore, apart from the tremendous industrial applications, the LiP from Pseudomonas fluorescence LiP-RL5 could be a potential biocatalyst for the detoxification of synthetic dyes.

Coupling Nanoscale Precision with Multiscale Imaging: A Multifunctional Near-Infrared Dye for the Brain.

Live imaging of primary neural cells is crucial for monitoring neuronal activity, especially multiscale and multifunctional imaging that offers excellent biocompatibility. Multiscale imaging can provide insights into cellular structure and function from the nanoscale to the millimeter scale. Multifunctional imaging can monitor different activities in the brain. However, this remains a challenge because of the lack of dyes with a high signal-to-background ratio, water solubility, and multiscale and multifunctional imaging capabilities. In this study, we present a neural dye with near-infrared (NIR) emissions (>700 nm) that enables ultrafast staining (in less than 1 min) for the imaging of primary neurons. This dye not only enables multiscale neural live-cell imaging from vesicles in neurites, neural membranes, and single neurons to the whole brain but also facilitates multifunctional imaging, such as the monitoring and quantifying of synaptic vesicles and the changes in membrane potential. We also explore the potential of this NIR neural dye for staining brain slices and live brains. The NIR neural dye exhibits superior binding with neural membranes compared to commercial dyes, thereby achieving multiscale and multifunctional brain neuroimaging. In conclusion, our findings introduce a significant breakthrough in neuroimaging dyes by developing a category of small molecular dyes.

Detection of trace levels of selected allergic chemicals in commercial hair dyes in local market of Jeddah, Saudi Arabia

Hair dyes are now commonly used in Saudi Arabia, and other nations across the world, to cover up grey hairs and/or to modify the natural color of the hair. The principal ingredients of hair dyes are aromatic amines and phenols and which most likely cause allergic reactions, irritated skin, and even cancer in certain cases. Thus, the current study reports the separation and subsequent identification of four chemical constituents namely p-Phenylenediamine (PPD), 3-aminophenol (3AP), resorcinol (RES), and 2-methylresorcinol (2MRS) in 26 commercial hair dyes that represent ten famous brands available in the local market of Jeddah city, Saudi Arabia. High-performance liquid chromatography (HPLC) technique was successfully employed to identify the four chemical compounds using methanol-aqueous solution (10:90 v/v) containing diethanolamine (0.05 %) and ammonium acetate (0.02 M) at pH 5.2 as a proper mobile phase. The column was 150 × 4.6 mm ID and 5 µm Eclipse Plus C18 column and the retention times were 1.26, 3.16, 4.99 and 6.01 min for PPD, 3AP, RES, and 2MRS, respectively. The four standards PPD, 3AP, RES, and 2MRS at 254 nm displayed excellent linear calibration plots in the concentration range 5–100 µg/mL with acceptable correlation coefficients (R2) of 0.9964, 0.9980, 0.9952 and 0.9961, respectively. The low limits of detection (LOD) and quantification (LOQ) based on the standard deviation of the response and the slopes of the plots were found to be equal 7.17, 5.39, 8.33, and 7.47 µg/mL and 23.91, 17.97, 27.75, 24.89 µg/mL for PPD, 3AP, RES, and 2MRS, respectively.

Adsorption kinetics and thermodynamics of metal complex acid dyes on silk fabric

This study reports the adsorption phenomena of metal complex acid dyes onto silk fabric. Two commercial metal complex acid dyes namely Bestalan Yellow SF and Bestalan Navy SF were adsorbed onto degummed silk fabric. The functional properties and surface morphology of silk fabric were investigated with FT-IR spectroscopy and FE-SEM respectively. The typical absorption band of C = O stretching was found at 1620 cm−1 indicating amide I structure and C-N stretching as well as N-H bending vibrations were observed at 1510 cm−1 suggesting the β-sheet crystallites of amide I and amide II silk proteins. The effectiveness of degumming performance was confirmed by SEM images. The adsorption of dyes by silk fabric was investigated with respect to pH, initial dye bath concentration, and contact time. It was found that the adsorption of dye onto silk fabric was highly influenced by the dye bath pH, initial dye concentration, and contact time. The higher dye adsorption was observed at acidic dye bath condition (pH = 3.5). The adsorption of dye was also increased with the increase of the initial dye bath concentration. The dyes adsorption reached at equilibrium condition after 80 min. The adsorption isotherm and kinetics were also evaluated based on the experimental results. The adsorption pattern fitted well to the Langmuir adsorption isotherm with high correlation coefficient (R 2>0.97) for both dyes. The kinetic parameters suggested that the pseudo-second-order model is more suitable compare to the pseudo-first-order model considering the higher regression coefficients ( R 2 = ∼ 0.99 ) . The maximum adsorption of Bestalan Yellow SF and Bestalan Navy SF was found to be 232.5 and 222.2 mg/g respectively. The thermodynamic data were studied at 25, 40 and 60 °C. The change of Gibbs free energy of the system was positive indicating the spontaneous nature of the adsorption. The values of ΔH (-4.68 kJ/mole −3.65 kJ/mole) suggested the exothermic environment and the negative values of ΔS (-0.035 and −0.034 kJ/mole/k) advocated the good interaction between the metal complex acid dyes and silk fabric. The Langmuir adsorption model and pseudo-second-order kinetic suggested that the dyeing of metal complex acid dyes on silk fabric was controlled by ion-exchange chemical reaction.

Synthesis, characterization and evaluation of new alternative ruthenium complex for dye sensitized solar cells

For first time, new innovative ruthenium N3-Dye anchored with selenium (Se) and N3 dye anchored with sulphur atoms were synthesized in a good yield. Dyes are applied and evaluated in performance of dye sensitized solar cell. N3–Se dye showed superior photochemical& electrochemical behavior and high rate electron transfer across anode surface than N3–S dye. The better optical and electrochemical activities would make Se-dye a candidate for applications in solar cells. Half life time of N3–S showed a single exponential decay with an average lifetime of 0.8 ns. For N3–Se dye, decay curve was fitted by sum two exponential functions with 75% and 25% counts have 2.5 ns and 30 ns respectively. Solar cells were fabricated and analyzed to determine their solar-to-electric conversion efficiency under standard AM 1.5 sunlight. Commercial N3 dyes showed current density (Jsc) of 17.813 mA cm−2, open circuit potential (Voc) of 0.678 V, filling factor (FF) of 0.607 and conversion efficiencies (η) of 7.3%. Corresponding values for N3–S dye, Jsc 11.2 mA cm−2, Voc 0.650 V, FF 0.681 and η 5%. Se–N3 dye, showed Jsc = 6.670 mA cm−2, Voc = 0.6004 V, FF = 0.77 and η = 3.09%. Long lifetime of N3–Se caused low practical performance.

Assembling-induced redox property adjustment of Fe(III)/Fe(IV) electroredox couple-based commercial dye catholyte via bio-inspired multicoordination sphere construction strategy for stable aqueous redox flow batteries

Redox flow batteries (RFBs) are capable of storing and integrating indirect clean energy. This is due to their scalability, safety, and reliability, as well as their independent decoupling of power and energy. Aqueous organic redox flow batteries (AORFBs) have redox-active materials that are composed of abundant elements, have tunable redox potential, greater solubility, and lower cost. Here We propose the use of an inexpensive commercial dye, naphthol green B (NGB), as a catholyte material for AORFBs. This is the first time that NGB has been utilized in the Fe(III)/Fe(IV) electroredox couple, demonstrating a high redox potential of 0.73 V vs. NHE under neutral conditions. Experimental characterizations and theoretical simulations indicate that hydroxypropyl-β-cyclodextrin (HP-β-CD) can serve as the secondary and outer coordination sphere of NGB, enhancing its electrochemical performance and stability, while also preventing transmembrane crossover. In the NGB/K3Fe(CN)6 test with HP-β-CD symmetric battery, NGB demonstrated excellent electrochemical stability. When used as anolyte with 1,1′-bis(3-sulfonatopropyl)-4,4′-bipyridinium (Spr)2V, the NGB/(Spr)2V AORFB with HP-β-CD demonstrated exceptional cycling performance at current rates ranging from 5 to 30 mA cm−2. It is worth noting that the NGB/(Spr)2V AORFB maintained over 99 % of its total capacity or experienced less than 0.00125 % capacity decay per cycle, with an average Coulombic efficiency of almost 100 % over 800 cycles at 10 mA cm−2. NGB is a novel and superior catholyte that offers multiple options for studying AORFBs and the potential for large-scale energy storage applications.

Estimation for Raw Material Plants of a Henna Product Using LC-High Resolution MS and Multivariate Analysis.

Henna is a plant-based dye obtained from the powdered leaf of the pigmented plant Lawsonia inermis, and has often been used for grey hair dyeing, treatment, and body painting. As a henna product, the leaves of Indigofera tinctoria and Cassia auriculata can be blended to produce different colour variations. Although allergy from henna products attributed to p-phenylenediamine, which is added to enhance the dye, is reported occasionally, raw material plants of henna products could also contribute to the allergy. In this study, we reported that raw material plants of commercial henna products distributed in Japan can be estimated by LC-high resolution MS (LC-HRMS) and multivariate analysis. Principal Component Analysis (PCA) score plot clearly separated 17 samples into three groups [I; henna, II; blended henna primarily comprising Indigofera tinctoria, III; Cassia auriculata]. This grouping was consistent with the ingredient lists of products except that one sample listed as henna was classified as Group III, indicating that its ingredient label may differ from the actual formulation. The ingredients characteristic to Groups I, II, and III by PCA were lawsone (1), indirubin (2), and rutin (3), respectively, which were reported to be contained in each plant as ingredients. Therefore, henna products can be considered to have been manufactured from these plants. This study is the first to estimate raw material plants used in commercial plant-based dye by LC-HRMS and multivariate analysis.

Solvent-assisted salt-free reactive dyeing of cotton fabric

The objective of this study was to establish a solvent-assisted salt-free dyeing method for cotton fabric utilizing commercially available reactive dyes. In this study, the feasibility of substituting water as the dyeing medium with environmentally friendly solvents, specifically ethanol (EtOH), isopropyl alcohol (IPA), and propanol (PrOH), was investigated. Eight commercial reactive dyes, each possessing distinct chemical structures, were examined with various dyeing characteristics including exhaustion, fixation, and fastness properties, in the presence of various alcohols. However, solvent-assisted dyeing exhibited comparable or enhanced color strength (K/S) values, exhaustion, and fixation rates compared to conventional aqueous dyeing. For instance, the RR35 dye demonstrated a substantial increase in K/S values with PrOH, EtOH, and IPA, ranging from 115 to 369% improvement. The substitution of alcohol for water did not affect the wash, rub, and light-color fastness properties, as these properties remained consistently excellent. Solvent-assisted salt-free dyeing of cotton fabrics offers a promising solution to address the environmental impacts of traditional water-based dyeing methods by eliminating the requirement for water and salt. Overall, this study presents a solvent-assisted salt-free dyeing technique and contributes to the field by offering detailed insights into its mechanisms and performance. Our research has the potential to reduce water consumption, eliminate salt usage, and mitigate environmental pollution.

A clinical study and laboratory evaluation of the cardiac and hepatic toxic effects of paraphenylenediamine

Introduction Paraphenylenediamine is the main component in many commercial hair dyes, and can produce severe local and systemic toxicity reactions after acute ingestion or dermal absorption. The aim of this study was to assess the factors contributing to morbidity and mortality in cases of acute paraphenylenediamine poisoning, with a focus on evaluating the resultant hepatic and cardiac toxicity. Methods This observational study was conducted on patients with acute paraphenylenediamine poisoning presenting to Sohag University Hospitals, and included a retrospective part from February 2021 to January 2022 and a prospective part from February 2022 to July 2022. Clinical data were extracted and receiver operating characteristic curves created to identify prognostic markers. Results Among 50 eligible patients 39 (78 percent) recovered, and 11 (22 percent) died or had permanent complications. Angioedema and anuria were the most frequent features in complicated cases. By receiver operating characteristic analysis, either an increase in aspartate aminotransferase activity greater than 644 IU/L or alanine aminotransferase activity greater than 798 IU/L, a time delay to presentation of greater than 4.5 hours, and a pH of less than 7.32 were associated with a significant increase in morbidity and mortality. While cardiac enzyme activities, and concentrations of blood urea nitrogen and creatinine increased in most cases, they were not associated with mortality. Discussion Management of patients with paraphenylenediamine poisoning is mainly supportive, as there is no specific antidote. Respiratory failure and kidney failure are the most life threatening complications. Hepatoxicity and cardiotoxicity also occur. The ability to predict the events can help guide patient disposition and care. Conclusion Elevated liver enzyme activities, increased time delay to admission, decreased pH, and the presence of angioedema and anuria can be used as predictors of morbidity and mortality in patients with acute paraphenylenediamine poisoning.

Single-step synthesis of MgAl2O4/MgO nanocomposites from MgAl scraps by thermal plasma technique for bi-functional applications of supercapacitor and waste-water treatment

Plasma-based methods present a highly efficient approach for reclaiming valuable metals and nanoparticles from discarded metal scraps and minerals. In this research, we employed the thermal plasma arc discharge (TPAD) method to synthesize mixed-phase spinal-type magnesium aluminate and magnesium oxide (MgAl2O4/MgO) nanocomposites ranging in size from 10 to 120 nm, using discarded MgAl alloy waste scraps as the primary material. By employing comprehensive characterization techniques such as powder X-ray diffraction (XRD), transmission electron microscopy (TEM), and energy dispersive X-ray analysis (EDS), we successfully confirmed the formation of highly crystalline MgAl2O4/MgO nanocomposites, showcasing a nearly spherical morphology. The surface area of the prepared nanocomposites was investigated using Brunauer-Emmett-Teller (BET) analysis; the values are 51.3 m2g-1. The synthesized MgAl2O4/MgO nanocomposites displayed exceptional photocatalytic activity toward industrial wastewater and commercial dye. Moreover, investigated the storage properties of MgAl2O4/MgO nanocomposites as an electrode material, revealing a good specific capacitance of 379.2 F/g at a current density of 1 A/g, demonstrating pseudocapacitive behavior. These results offer valuable insights into sustainable waste utilization and the development of high-performance nanomaterials for practical applications in various fields.

Highly Efficient, Noble-Metal-Free, Fully Aqueous CO2 Photoreduction Sensitized by a Robust Organic Dye.

The development of efficient, selective, and durable CO2 photoreduction systems presents a long-standing challenge in full aqueous solutions owing to the presence of scarce CO2 and the fierce competition against H2 evolution, which is even more challenging when noble metals are not utilized. Herein, we present the facile decorations of four phosphonic acid groups on a donor-acceptor-type organic dye to obtain a water-soluble photosensitizer (4P-DPAIPN), which succeeds the excellent photophysical and photoredox properties of its prototype, exhibiting long-lived delayed fluorescence (>10 μs) in aqueous solutions. Combining 4P-DPAIPN with a cationic cobalt porphyrin catalyst has accomplished record-high apparent quantum yields of 9.4-17.4% at 450 nm for CO2-to-CO photoconversion among the precedented systems (maximum 13%) in fully aqueous solutions. Remarkable selectivity of 82-93% and turnover number of 2700 for CO production can also be achieved with this noble-metal-free system, outperforming a benchmarking ruthenium photosensitizer and a commercial organic dye under parallel conditions. Such high performances of 4P-DPAIPN can be well maintained under real sunlight. More impressively, no significant decomposition of 4P-DPAIPN was detected during the long-term photocatalysis. Eventually, the photoinduced electron transfer pathways were proposed.