Search Results (150)

Supercapacitors, with their remarkable attributes such as including a high power density, an extended cycle life, and inherent safety, have emerged as a major research area for electrochemical energy storage. In this paper, phenylenediamine and glyoxal were used as raw material to prepare p-phenylenediamine glyoxal (PGo) with one single step. p-phenylenediamine glyoxal-ferrocene (PGo-Fc_x, x = 1, 0.3, 0.2, 0.1) composites were synthesized based on a poly-Schiff base. FTIR and XRD results indicated that ferrocene doping preserves the intrinsic PGo framework while inducing grain refinement, as evidenced by the narrowing of the XRD diffraction peaks. SEM observations further revealed distinct morphological evolution. CV (cyclic voltammetry), EIS (electrochemical impedance spectroscopy), and GCD (galvanostatic charge–discharge) were conducted on PGo-Fc_x in order to examine its electrochemical performance. The PGo-Fc_0.3 in PGo-Fc_x electrode material had a specific capacitance of 59.6 F/g at a current density of 0.5 A/g and 36 F/g at a current density of 10 A/g. Notably, even after undergoing 5000 charging–discharging cycles at 10 A/g, the material retained 76.2% of its specific capacitance compared to the initial cycle. Therefore, taking conductive polymers and metal oxide materials for modification can improve the stability and electrochemical performance of supercapacitors. Full article

In recent years, tires have become a prominent concern for researchers and environmentalists in regard to their potential threat of tire-derived pollutants (TDPs) to human health. Among these pollutants, N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD) and its oxidized form, 6PPD-quinone (6PPD-Q), have been of primary interest due their ubiquity in urban environments, and their potential negative effects on human health. This review provides a summary of human health implications of TDPs, including 6PPD and 6PPD-Q. For the methodology, datasets were collected from the literature sources, including sources, formations and ecological effects of these pollutants, and pathways of human exposure and public health significance. Urban soils are key for services including carbon storage, water filtration, and nutrient cycling, underpinning urban ecosystem resilience. Soil degradation through compaction, sealing, and pollution, particularly by pollutants from tire wear, destroys these functions, however. These pollutants disturb the soil microbial communities, leading to a loss of diversity, an increase in pathogenic species, and changes in metabolism, which in turn can impact human health by increasing disease transmission and diseases of the respiratory systems. Incorporating green-infrastructure practices can enhance the ecosystem service potentials of urban soils and contribute to sustainable, climate-resilient urban city development. These findings underscore the pressing need for a coordinated international campaign to study chronic health effects and science informed policy frameworks to address this ubiquitous environmental health concern—an issue that crosses urban water quality, environmental justice, and global management of tire pollution. Full article

Tyre wear particles (TWPs), generated from tyre-road abrasion, are a pervasive and under-regulated environmental pollutant, accounting for a significant share of global microplastic contamination. Recent estimates indicate that 1.3 million metric tons of TWPs are released annually in Europe, dispersing via atmospheric transport, stormwater runoff, and sedimentation to contaminate air, water, and soil. TWPs are composed of synthetic rubber polymers, reinforcing fillers, and chemical additives, including heavy metals such as zinc (Zn) and copper (Cu) and organic compounds like polycyclic aromatic hydrocarbons (PAHs) and N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD). These constituents confer persistence and bioaccumulative potential. While TWP toxicity in aquatic systems is well-documented, its ecological impacts on terrestrial environments, particularly in agricultural soils, remain less understood despite global soil loading rates exceeding 6.1 million metric tons annually. This review synthesizes global research on TWP sources, environmental fate, and ecotoxicological effects, with a focus on soil–plant systems. TWPs have been shown to alter key soil properties, including a 25% reduction in porosity and a 20–35% decrease in organic matter decomposition, disrupt microbial communities (with a 40–60% reduction in nitrogen-fixing bacteria), and induce phytotoxicity through both physical blockage of roots and Zn-induced oxidative stress. Human exposure occurs through inhalation (estimated at 3200 particles per day in urban areas), ingestion, and dermal contact, with epidemiological evidence linking TWPs to increased risks of respiratory, cardiovascular, and developmental disorders. Emerging remediation strategies are critically evaluated across three tiers: (1) source reduction using advanced tyre materials (up to 40% wear reduction in laboratory tests); (2) environmental interception through bioengineered filtration systems (60–80% capture efficiency in pilot trials); and (3) contaminant degradation via novel bioremediation techniques (up to 85% removal in recent studies). Key research gaps remain, including the need for long-term field studies, standardized mitigation protocols, and integrated risk assessments. This review emphasizes the importance of interdisciplinary collaboration in addressing TWP pollution and offers guidance on sustainable solutions to protect ecosystems and public health through science-driven policy recommendations. Full article

P-phenylenediamines (PPDs) and their quinone derivatives (PPDQs), emerging pollutants widespread in urban environments, exhibit biotoxicological risks. Epidemiological studies suggest their adverse impacts on intestinal health, yet the underlying mechanisms remain unclear. This study aimed to investigate the potential mechanisms of enterotoxicity induced by 13 PPDs and PPDQs using network toxicology and molecular docking approaches. Through the SuperPred, STITCH, GeneCards, and OMIM databases, 182 potential targets associated with PPD- and PPDQ-induced enterotoxicity were identified. Thirty hub targets, including SRC, EGFR, CASP3, and others, were prioritized using STRING and Cytoscape tools. GO and KEGG enrichment analyses via the DAVID and FUMA databases revealed significant enrichment of core enterotoxicity-related targets in the MAPK signaling pathway and the calcium signaling pathway. Molecular docking with AutoDock confirmed strong binding affinities between PPDs/PPDQs and core targets. These results suggest that PPDs and PPDQs may promote the onset and progression of bowel cancer and intestinal inflammation by modulating cancer cell death, proliferation, and inflammatory signaling pathways. This research provides a theoretical framework for elucidating the molecular mechanisms of PPD- and PPDQ-induced enterotoxicity, offering insights for the prevention of associated diseases. Full article

Free chlorine (FC) plays a crucial role in ensuring the safety of drinking water by effectively inactivating pathogenic microorganisms. However, traditional methods for measuring FC levels often require specialized equipment and laboratory settings, limiting their accessibility and practicality for on-site or point-of-use monitoring. QR Codes are powerful machine-readable patterns that are used worldwide to encode information (i.e., URLs or IDs), but their computer vision features allow QR Codes to act as carriers of other features for several applications. Often, this capability is used for aesthetics, e.g., embedding a logo in the QR Code. In this work, we propose using our technique to build back-compatible Color QR Codes, which can embed dozens of colorimetric references, to assist in the color correction to readout sensors. Specifically, we target two well-known products in the HORECA (hotel/restaurant/café) sector that qualitatively measure chlorine levels in samples of water. The two targeted methods were a BTB strip and a DPD powder. First, the BTB strip was a pH-based indicator distributed by Sensafe^®, which uses the well-known bromothymol blue as a base-reactive indicator; second, the DPD powder was a colorimetric test distributed by Hach^®, which employs diethyl-p-phenylenediamine (DPD) to produce a pink coloration in the presence of free chlorine. Custom Color QR Codes were created for both color palettes and exposed to several illumination conditions, captured with three different mobile devices and tested over different water samples. Results indicate that both methods could be correctly digitized in real-world conditions with our technology, rendering a 88.10% accuracy for the BTB strip measurement, and 84.62% for the DPD powder one. Full article

Vitamins are crucial micro-nutrients for overall well-being, making continuous monitoring essential. There are demands to provide an alternative detection, especially using a portable detection or a point-of-care-testing (POCT) device. One promising approach is employing an in situ electro-polymerised MIP (eMIP), which offers a straightforward polymerisation technique on screen-printed electrodes (SPEs). Here, we report a review based on three databases (PubMed, Scopus, and Web of Science) from 2014 to 2024 using medical subject heading (MeSH) terms “electrochemical polymerisation” OR “electropolymerisation” crossed with the terms “molecularly imprinted polymer” AND “vitamin A” OR “vitamin D” OR “vitamin E” OR “vitamin K” OR “fat soluble vitamin” OR “vitamin B” OR “vitamin C” OR “water soluble vitamin”. The resulting 12 articles covered the detection of vitamins in ascorbic acid, riboflavin, cholecalciferol, calcifediol, and menadione using monomers of catechol (CAT), 3,4-ethylenedioxythiophene (EDOT), o-aminophenol (oAP), o-phenylenediamine (oPD), pyrrole, p-aminophenol (pAP), p-phenylenediamine (pPD), or resorcinol (RES), using common bare electrodes including graphite rod electrode (GRE), glassy carbon electrode (GCE), gold electrode (GE), and screen-printed carbon electrode (SPCE). The most common electrochemical detections were differential pulse voltammetry (DPV) and linear sweep voltammetry (LSV). The imprinting factor (IF) of the eMIP-modified electrodes were from 1.6 to 21.0, whereas the cross-reactivity was from 0.0% to 29.9%. Several types of food and biological samples were tested, such as supplement tablets, poultry and pharmaceutical drugs, soft drinks, beverages, milk, infant formula, human and calf serum, and human plasma. However, more discoveries and development of detection methods needs to be performed, especially for the vitamins that have not been studied yet. This will allow the improvement in the application of eMIPs on portable-based detection and POCT devices. Full article

A compatibilizer for low-density polyethylene (LDPE)/poly(ethylene terephthalate) (PET) blends was developed. This compatibilizer consists of amine-functionalized PET, which is blended with maleated polyethylene to form a copolymer. The goal is to use this compatibilizer in the future for recycling plastic waste from the marine environment. Fourier-transform infrared spectroscopy confirmed the successful incorporation of amine groups into PET chains through the addition of p-phenylenediamine in a molten state. An increase in diamine content allowed for the visualization of three bands where PET reacted with the diamine. Differential scanning calorimetry suggested that the polyester chains were grafted onto the maleated polyethylene backbone, with crystallinity increasing up to 2.5% diamine content. Scanning electron microscopy (SEM) images showed that the LDPE/PET blend resulted in a continuous polyethylene matrix with a dispersed polyester phase. The blend compatibilized with modified maleated polyethylene, and functionalized PET exhibited an improved interface. Oscillatory rheology and dynamic mechanical analysis indicated that the developed compatibilizer positively impacted the mechanical properties of the compatibilized LDPE/PET blends. This new approach enables the creation of innovative strategies for enhancing the properties of pre-existing polyolefin/polyester recycled blends. Full article

N-(1,3-dimethylbutyl)-N’-phenyl-p-benzoquinone (6PPD-Q) is an emerging environmental contaminant that is widely distributed in aquatic environments and presents significant toxicological risks to aquatic organisms. As 6PPD-Q is primarily derived from oxidative transformation of the tire antioxidant N-(1,3-dimethylbutyl)-N’-phenyl-p-phenylenediamine (6PPD), its persistence and potential for bioaccumulation in aquatic organisms have raised widespread concerns. This study reviews the environmental sources, spatial distribution, migration, and transformation behaviors of 6PPD-Q, as well as its degradation mechanisms in different environmental media. Additionally, this review systematically explores the toxicological effects of 6PPD-Q on aquatic organisms, including its physiological, biochemical, and molecular impacts on fish, crustaceans, mollusks, and algae, with a focus on potential toxicological mechanisms. Finally, we discuss the limitations of current research on 6PPD-Q and propose key directions for future studies, including long-term ecological risk assessments, mechanisms of bioaccumulation, metabolic pathway analysis, and optimization of pollution control strategies, aiming to provide a scientific basis for the ecological risk assessment and pollution management of 6PPD-Q. Full article

A method for the determination of trace selenium in water enriched by metal–organic−framework material (MIL−125−NH₂) and reversed−phase ultra−high−performance liquid chromatography−diode array detection (UPLC−DAD) was established. The MIL−125−NH₂ material, synthesized by the microwave method, was characterized by SEM, XRD, and FT−IR. The MIL−125−NH₂ material was added to the water sample to enrich the selenium, the enriched selenium was desorbed with dilute HCl, and then the derivative reaction with 0.1 mol·L⁻¹ 4−nitro−o−phenylenediamine was performed to produce piaselenole. After extraction with cyclohexane, the retention time and the spectrogram were qualitatively detected by a liquid chromatography−diode array detector, and the peak area was quantitatively detected. The pH, time, amount of material, extractant, and other conditions of derivation and enrichment were optimized in the experiment, and the methodology was verified under optimized conditions. The results showed that the linear correlation coefficient R² was 0.9998, the detection limit of 0.13 μg·L⁻¹ without enrichment was close to that of the ICP−MS method, the detection limit after 10−fold enrichment was 0.013 μg·L⁻¹, the RSD was 0.7~2.7%, and the recovery was 87.8~102.1%, in the range of 2~1000 μg·L⁻¹. Therefore, the method can be applied for the determination of trace selenium in tap water, river water, mountain spring water, packaged drinking water, and industrial sewage. Full article

As a porous crystalline material, covalent organic frameworks (COFs) have attracted significant attention due to their extraordinary features, such as an ordered pore structure and excellent stability. Synthesized through the aldehyde amine condensation reaction, TpPa-1 COFs (Triformylphloroglucinol-p-Phenylenediamine-1 COFs) were blended with cellulose acetate (CA) to form a casting solution. The TpPa-1 COF/CA ultrafiltration membrane was then prepared using the non-solvent-induced phase inversion (NIPS) method. The influence of TpPa-1 COFs content on the hydrophilicity, stability and filtration performance of the modified membrane was studied. Due to the hydrophilic groups in TpPa-1 COFs and the network structure formed by covalent bonds, the modified CA membranes exhibited higher hydrophilicity and lower protein adsorption compared with the pristine CA membrane. The porous crystalline structure of TpPa-1 COFs increased the water permeation path in the CA membrane, improving the permeability of the modified membrane while maintaining an outstanding bovine serum albumin (BSA) rejection. Furthermore, the addition of TpPa-1 COFs reduced protein adsorption on the CA membrane and overcame the trade-off between permeability and selectivity in CA membrane bioseparation applications. This approach provides a sustainable method for enhancing membrane performance while enhancing the application of membranes in protein purification. Full article

Coccidiosis in chickens is a parasitic disease caused by Eimeria species, resulting in significant economic losses to the poultry industry. Among these species, Eimeria tenella is considered the most virulent pathogen, with its infection strongly associated with the apoptotic response of host cells. Eimeria tenella modulates host cell apoptosis in a stage-specific manner, suppressing apoptosis in the early phase to promote its intracellular development and triggering apoptosis in later stages to facilitate parasite egress and disease progression. This study established an in vitro infection model using 60 fifteen-day-old chick embryo cecal epithelial cells and infecting the cells with Eimeria tenella sporozoites at a 1:1 ratio of host cells to sporozoites. The aim was to examine the relationship between parasitic infection and the apoptotic response of host cells in the chick embryo cecal epithelial cells infected with E. tenella. The roles of the mitochondrial permeability transition pore (MPTP) and cytochrome c in intrinsic apoptosis were examined through the application of cyclosporine A (CsA), N, N, N’, N’-tetramethyl-1,4-phenylenediamine (TMPD), and ascorbate (Asc). TUNEL staining, ELISA, and flow cytometry were performed to evaluate apoptotic rates. CsA, TMPD, and Asc significantly (p < 0.01) decreased cytochrome c release, caspase-9 activation, and apoptotic rates from 24 to 120 h post-E. tenella infection. These findings highlight the significance of cytochrome c-mediated, mitochondria-dependent apoptotic pathways in parasitized chick embryo cecal epithelial cells. Full article

Electro-chlorination (E-Cl) is an emerging and promising electrochemical advanced oxidation technology for wastewater treatment with the advantages of high efficiency, deep mineralization, a green process, and easy operation. It was found that the mechanism of pollutant removal by electro-chlorination mainly involves an indirect oxidation process, in which pollutant removal is mainly driven by the intermediate active species, especially RCS and chlorine radicals, with a strong oxidization ability produced at the anodes. In this work, we summarized the principles and pathways of the removal/degradation of pollutants (organic pollutants and ammonia nitrogen) by E-Cl and the major affecting factors including the applied current density, voltage, electrolyte concentration, initial pH value, etc. In the E-Cl system, the DSA and BDD electrodes were the most widely used electrode materials. The flow-through electrode reactor was considered to be the most promising reactor since it had a high porosity and large pore size, which could effectively improve the mass transfer efficiency and electron transfer efficiency of the reaction. Of the many detection methods for chlorine radicals and RCS, electron paramagnetic resonance (EPR) and spectrophotometry with N, N-diethyl-1,4-phenylenediamine sulfate (DPD) as the chromogenic agent were the two most widely used methods. Overall, the E-Cl process had excellent performance and prospects in treating salt-containing wastewater. Full article

(1) Background: N-(1,3-Dimethylbutyl)-N′-phenyl-p-phenylenediamine-quinone (6PPDQ), as a newly discovered environmental toxin, has been found more frequently in our living conditions. The literature reports that damage to the reproductive and cardiovascular system is associated with exposure to 6PPDQ. However, the relationship between 6PPDQ and cancer still requires more investigation. This research aims to investigate the association between 6PPDQ and prostate cancer. (2) Methods and Results: Based on the data retrieved from the Pharmmapper, CTD, SEA, SwissTargetPrediction, GeneCard, and OMIM databases, we summarized 239 potential targets utilizing the Venn tool. Through the STRING network database and Cytoscape software, we constructed a PPI network and confirmed ten core targets, including IGF1R, PIK3R1, PTPN11, EGFR, SRC, GRB2, JAK2, SOS1, KDR, and IRS1. We identified the potential pathways through which 6PPDQ acts on these core targets using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses. Ultimately, through molecular docking methods, 6PPDQ binds closely with these ten core targets. These findings indicate that 6PPDQ may influence the proteins related to prostate cancer and may be linked to prostate cancer via several known signaling pathways. (3) Conclusions: This article employs innovative network toxicology to elucidate the prostate carcinogenic effects of 6PPDQ through its modulation of specific vital genes and signaling pathways, thereby establishing a foundational platform for future investigations into the impact of 6PPDQ on prostate cancer and potentially other tumors. Full article

Hexavalent chromium, one of the heavy metal pollutants in water, harms the ecological environment and human health. In this work, an aniline-p-phenylenediamine copolymer has been prepared by chemical oxidative polymerization to remove the hexavalent chromium (Cr(VI)) from wastewater. The results show that when the initial Cr(VI) concentration is 1.5 mg·L⁻¹, the removal percentage (RP%) of Cr(VI) could reach 94.84% after 180 s of treatment. The RP% of Cr(VI) increases with the dosage of copolymers and decreases with an increase in the initial Cr(VI) concentration. Additionally, the RP% of Cr(VI) removal reaches a maximum of 97.70% with a pH value of 1.0. The Cr(VI) removal kinetics of the copolymers follows a pseudo-first-order chemical reaction model. The X-ray photoelectron spectroscopy (XPS) results demonstrate that the Cr(VI) removal mechanism by the aniline-p-phenylenediamine copolymer is a redox reaction. The positive value of ΔH° and negative value of ΔG° affirm that the Cr(VI) removal process by aniline-p-phenylenediamine copolymer is endothermic, thermodynamically achievable, and spontaneous. Full article

The early diagnosis of tumorigenesis is crucial for clinical treatment, but the resolution and sensitivity of conventional short-wavelength biomarkers are not ideal because of the complicated interference in living tissue. Herein, a nicotinamide adenine dinucleotide (NAD⁺)-responsive probe with deep-red emissive ratiometric fluorescence was synthetized as a promising target for energy metabolism patterns during tumorigenesis. Interestingly, the solvents H₃PO₄ and 2,2′-dithiodibenzoic acid enhanced the red emission (640 and 680 nm) of o-phenylenediamine-based carbon dots (CDs), leading to the formation of a nanoscale graphite-like skeleton covered with -P=O, -CONH-, -COOH and -NH₂ on their surfaces. Meanwhile, this method exhibited high sensitivity to the discriminating target NAD⁺, with a detection limit of 63 μM due to the inner filter effect and fluorescence resonance energy transfer process between NAD⁺ and CDs, which is superior to the reported capillary electrophoresis and liquid chromatographic detection methods (the reported detection limit was about 0.2 mM) in complex biological samples and even cancer cells. Encouragingly, NAD⁺ significantly promoted nucleus-targeting fluorescence and cell migration compared to GSH and pH stimulation, which were gradually eliminated in human hepatocellular carcinoma (HepG2) cells after 2-deoxy-d-Glucose inhibited the glycolytic phenotype. The proposed method holds great potential for the temporal and spatial resolution of NAD⁺-dependent tumor diagnosis in complex living systems. Full article