Search Results (434)

The environmental concerns associated with the excessive use and improper disposal of plastic waste have led to increased interest in chemical recycling methods such as pyrolysis. In this study, waste plastic pyrolysis oil (WPPO) was evaluated as a potential feedstock to produce high-quality feedstock for lubricant base oils through hydroprocessing. WPPO was obtained via the thermal degradation of waste plastic at 400 °C under a nitrogen atmosphere using a 2 t/day pyrolysis reactor. The physicochemical properties of WPPO were analyzed, including the sulfur, chlorine, and metal contents. A series of Pt-supported catalysts based on different acidic supports (SAPO-11, SAPO-34, and Zeolite Y100) was prepared using an incipient wetness impregnation method and characterized by BET, XRD, and TPD techniques. The hydroprocessing reactions were conducted under varying temperature and pressure conditions to evaluate conversion and optimize product selectivity. The catalysts exhibited different surface areas, pore structures, and acidity profiles, which directly impacted their hydroprocessing performance. The results demonstrate that Pt/Y-100 exhibited the best upgrading performance among the tested catalysts, achieving an olefin-to-paraffin conversion of over 88.65% with a dominant paraffinic hydrocarbon distribution in the C15–C25 range under optimal conditions (300 °C and 40 bar). The results demonstrate that the conversion of olefins to paraffins in WPPO can be effectively controlled by tuning the reaction conditions and catalyst. Full article

This comprehensive review provides a consolidated and practically oriented overview of the Friedel–Crafts reaction in pharmaceutical synthesis, bringing together data from 93 peer-reviewed studies published between 1962 and 2025. Through a structured and comparative analysis of the literature retrieved from the Scopus and PubMed databases, this work integrates scattered information into a single, accessible resource, designed to guide researchers in drug discovery and development. The findings identify alkylation and acylation as the dominant Friedel–Crafts transformations, often enabling the synthesis of pharmacologically relevant scaffolds depending on substrate structure and the efficiency and selectivity of the catalytic system. These include compounds with anticancer, anti-inflammatory, and antimicrobial potential. Trends in catalyst and solvent selection highlight both the persistent reliance on classical Lewis acids in chlorinated media and a gradual interest in more sustainable alternatives, although their adoption remains system-dependent. By consolidating 63 years of research into a unified reference, this review underscores the versatility and enduring relevance of Friedel–Crafts methodologies in medicinal chemistry but also offers a data-driven foundation for their optimized and more sustainable application in future pharmaceutical development. Full article

The development of low-temperature, high-efficiency catalysts for the catalytic elimination of chlorinated volatile organic compounds (CVOCs) remains a significant challenge. Investigating the influence mechanism of catalyst physicochemical properties on chlorobenzene oxidation performance and degradation pathways is particularly important. CuO/WO₃ catalysts were developed using a hydrothermal method in this work. The effects of simultaneous or separate addition of ammonium sulphate and ammonium persulphate on the catalytic performance of the CuO/WO₃ series catalysts were investigated. The results showed that the introduction of ammonium sulphate alone can facilitate the formation of CuWO₄, thereby increasing the chemisorbed oxygen concentration of the CuO/WO₃, and making the overall structure of the catalyst looser and increasing the active sites on the catalyst surface. As the optimal catalyst, CuO/WO₃-2 exhibited 55.9% of chlorobenzene conversion and 32.9% of CO₂ selectivity at 500 °C. Interestingly, although the surface acidity in this work seemed to be one of the reasons for promoting the chlorobenzene oxidation, it could be clearly found that the strong solid acidity of WO₃ was actually a key factor in inhibiting the chlorobenzene oxidation. Finally, based on in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) analysis, the primary mechanism for chlorobenzene oxidation on CuO/WO₃ catalysts proceeds through a sequential conversion: chlorobenzene was first transformed into phenolic intermediates, followed by quinone compounds, maleates, aldehydes, bidentate carbonates, and ultimately carbonate species. Full article

Bromine, as a strategic fundamental chemical raw material, is crucial for modern industry, but the traditional chlorine displacement method poses safety risks in oilfield brine development and faces challenges like resource depletion and inefficient utilization. Addressing the need for high-concentration bromine brine development in underground oilfields, this study developed an electrochemical oxidation-based chlorine-free bromine extraction technology. Leveraging the standard redox potential difference between Br⁻ and Cl⁻ (0.271 V), the effective potential window for selective Br⁻ oxidation was determined as 1.0–1.52 V (vs. SHE) via linear sweep voltammetry (LSV). Within this window, efficient and preferential oxidation of Br⁻ over Cl⁻ and OH⁻ was achieved. In simulated brine with high chloride and low bromide concentrations, a Br⁻ conversion rate of 92.3% was attained with no Cl₂ generation. The self-designed zero-gap electrolyzer with carbon cloth as the anode reduced the reaction time by over 75% compared to a traditional H-type cell, oxidizing over 90% of Br⁻ within 12 min. Kinetic studies revealed that the reaction follows first-order kinetics, with current intensity positively correlated with Br⁻ concentration. Investigation of coexisting ions revealed that low concentrations of Cl⁻ promote the reaction, while high concentrations exert inhibitory effects. CO₃²⁻ exhibits a weak promoting effect, and Ca²⁺/Mg²⁺ show negligible impact. Notably, organic matter (e.g., ethylene glycol) concentrations exceeding 80 mg/L substantially compromise bromine recovery efficiency. This technology provides a feasible solution for the safe and green development of high-concentration bromine resources and holds significant importance for the upgrading of the bromine chemical industry. Full article

Parkinson’s disease (PD) is a complex neurodegenerative disorder influenced by age, genetic predispositions, and environmental exposures, with a growing global incidence. This review aims to summarize findings from ATSDR Toxicological Profiles, EPA Risk Assessments, and other sources of peer-reviewed literature to examine the potential associations between PD and select metals, pesticides, and chlorinated organic compounds. Additionally, it explores using computational toxicology methods to elucidate the interactions between specific chemicals, associated genes, and their possible roles in PD. A total of 29 substances were identified to be neurotoxic with direct or probable association with PD. Risk of disease onset or symptom exacerbation of PD has been linked to exposures to neurodegenerative metals, pesticides, chlorinated organic compounds, and other environmental toxicants, alongside intrinsic factors such as genetic predisposition and aging. Supporting evidence from neurotoxicological studies directly or possibly associated with PD are summarized in referenced toxicological profiles and EPA risk assessments. Genotoxic endpoints evaluated in exposure-induced neurodegeneration including oxidative stress, DNA strand breaks, mitochondrial dysfunction, impaired DNA repair, and telomere alterations may play a critical role in linking environmental exposures to PD pathogenesis. Although these endpoints represent imperative data gaps between environmental and genetic risk factors for PD, isolating individual substances may not be necessary for prevention, as many co-occur at contaminated sites or within certain occupations. Further research is needed to clarify causal relationships between environmental exposure and genotoxic endpoints seen in neurodegenerative processes that can also be seen in PD for consideration in the development of preventive and therapeutic strategies. Full article

Microbial contamination of table eggs remains an important food safety concern, largely due to the presence of Salmonella spp. on eggshell surfaces and the potential for cross-contamination along the collection, grading, and packing chain. Conventional sanitation practices, including chlorinated-water washing, can reduce surface microbial loads but may also present limitations related to cuticle alteration, process variability, water use, and the risk of recontamination when operational conditions are not tightly controlled. This review synthesizes evidence on non-thermal and selected mild thermal technologies for the surface decontamination of intact table eggs, including ultraviolet-C (UV-C) irradiation, pulsed light, ozone-based treatments (gas and microbubble systems), non-thermal plasma, plasma-activated water, and gas-phase hydroxyl radical processes. For each approach, antimicrobial performance is discussed alongside effects on eggshell integrity, cuticle preservation, and key quality indicators (e.g., Haugh unit, albumen pH, yolk color, and shell strength). Particular attention is given to industrial constraints that influence real-world performance, such as treatment uniformity and shading effects, humidity dependence, line speed, equipment integration, and validation criteria. A shared limitation of surface treatments is their inability to inactivate pathogens that have penetrated shell membranes or contaminated egg contents, underscoring the need to align technology selection with the targeted hazard and the regulatory context. Thus, available data indicate that non-thermal technologies can contribute to reducing eggshell contamination when properly optimized, although broader implementation will depend on standardized operating parameters, robust process validation, and regulatory acceptance within existing egg processing systems. Full article

Candidozyma auris is an emerging multidrug-resistant yeast that readily contaminates healthcare environments, persisting on dry surfaces and enabling transmission and difficult-to-control outbreaks. A systematic review of environmental hygiene interventions targeting C. auris was conducted, focusing on efficacy against planktonic cells and surface-associated biofilms (including dry-surface biofilms, DSB where available). PubMed and Scopus were searched for English-language records published from 1 January 2017 to 30 September 2025, and study selection followed PRISMA 2020. Thirty-six studies from nine countries met the inclusion criteria. These were predominantly laboratory efficacy evaluations using carrier/suspension or quantitative surface methods reporting log₁₀ Colony Forming Unit (CFU) reductions; only seven studies assessed biofilm-associated C. auris. Across clades I–IV, chlorine-based disinfectants and oxidizing chemistries (hydrogen peroxide/peracetic acid formulations) most consistently achieved high-level reductions (often ≥ 5 log₁₀ CFU) under label-relevant conditions. In contrast, products containing only quaternary ammonium compounds (QACs) frequently underperformed and demonstrated greater variability. No-touch methods, particularly 254 nm ultraviolet-C light (UV-C), provided meaningful adjunctive reductions, but were highly dependent on dose delivery and geometry, and evidence for ozone-based approaches was mixed. Limited data on C. auris DSBs suggest planktonic testing may overestimate real-world conditions and underscore the importance of endpoints, such as transfer prevention and regrowth suppression. Full article

Sulfide-based solid electrolytes are promising for all-solid-state sodium batteries due to their high ionic conductivity and facile processability, but their practical use is limited by moisture sensitivity and poor interfacial stability. To address these issues, Na_3−xPS_4−xM_x (M = F, Cl, Br, I) electrolytes were first synthesized as a preliminary study to evaluate the effect of halogen doping. Chlorine was identified as the most effective dopant and was therefore selected for a systematic investigation of doping concentration. Na_3−xPS_4−xCl_x (x = 0.1–0.3) electrolytes were prepared by solid-state sintering, and the optimum composition was determined to be Na_2.85PS_3.85Cl_0.15, which achieved a high ionic conductivity of 5.5 × 10⁻⁴ S·cm⁻¹ with a reduced activation energy of 33.3 kJ·mol⁻¹. When employed in TiS₂|Na_2.85PS_3.85Cl_0.15|Na₃Sn full cells, the optimized electrolyte enabled high initial capacity, excellent rate capability, and stable long-term cycling. These results highlight the effectiveness of Cl doping concentration control in enhancing both the intrinsic properties of Na₃PS₄-based electrolytes and the overall electrochemical performance of all-solid-state sodium batteries. Full article

Refuse-derived fuel (RDF) presents a viable strategy to concurrently address the challenges of municipal solid waste management and the need for alternative energy. In this context, the present review systematically synthesizes recent advances in RDF preparation, combustion behavior, and efficient utilization technologies. The study examines the full chain of RDF production—including waste selection, mechanical/optical/magnetic sorting, granulation, briquetting, and chemical modification—highlighting how pretreatment technologies influence fuel homogeneity, calorific value, and emissions. The thermochemical conversion characteristics of RDF are systematically analyzed, covering the mechanism differences among slow pyrolysis, fast pyrolysis, flash pyrolysis, pyrolysis mechanisms, catalytic pyrolysis, fragmentation behavior, volatile release patterns, and kinetic modeling using Arrhenius and model-free isoconversional methods (e.g., FWO). Special attention is given to co-firing and high-efficiency combustion technologies, including ultra-supercritical boilers, circulating fluidized beds, and rotary kilns, where fuel quality, ash fusion behavior, slagging, bed agglomeration, and particulate emissions determine operational compatibility. Integrating recent findings, this review identifies the key technical bottlenecks—feedstock variability, chlorine/sulfur release, heavy-metal contaminants, ash-related issues, and the need for standardized RDF quality control. Emerging solutions such as AI-assisted sorting, catalytic upgrading, optimized co-firing strategies, and advanced thermal conversion systems (oxy-fuel, chemical looping, supercritical steam cycles) are discussed within the broader context of carbon reduction and circular economy transitions. Overall, RDF represents a scalable, flexible, and high-value waste-to-energy pathway, and the review provides insights into future research directions, system optimization, and policy frameworks required to support its industrial deployment. Full article

Willows (genus Salix) are versatile plants with applications in construction, medicine, and biomass fuel in North America. Advances in breeding have improved willow clones for higher yields and pest resistance, but the chemical content and distribution across different plant parts remain poorly understood. This study examined the variation in chemical elements (carbon, hydrogen, nitrogen, sulfur, chlorine, and ash) across six willow clones (India, Jorr, Olof, Otisco, Preble, and Tora) and three tissue types (wood, bark, twigs). We also compared freeze-drying and oven-drying methods to assess their impact on chemical content. Freeze-dried samples generally exhibited higher carbon and hydrogen concentrations than oven-dried samples, with statistically significant differences primarily observed for carbon, while nitrogen showed no overall significant difference between drying methods. Chemical composition varied among clones, although no single clone consistently dominated across all chemical parameters. In contrast, pronounced tissue-type differences were observed: bark had higher nitrogen, carbon, sulfur, chlorine, and ash contents, whereas wood exhibited relatively higher hydrogen concentrations, with twigs showing intermediate values. These findings suggest that accounting for tissue-specific chemical differences can improve the selection and utilization of willow biomass and increase the accuracy of ecological assessments, including carbon storage estimates. The findings of this study indicate that oven-drying should remain in use within the bioenergy sector, whereas freeze-drying ought to become the preferred standard for carbon-accounting protocols. Full article

New arylbenzofuran derivatives were designed, synthesized, and evaluated as potential inhibitors of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). Five hybrid compounds (31–35) feature a 2-phenylbenzofuran core linked via a heptyloxy spacer to an N-methylbenzylamine moiety, to enhance interactions within the active site of BChE. Biological evaluation revealed that brominated derivatives 34 and 35 showed the highest cholinesterases (ChE) inhibition compared to their chlorinated analogs, with compound 34 showing the highest activity for both AChE (IC₅₀ = 27.7 μM) and BChE (IC₅₀ = 0.7 μM). These compounds proved to be non-cytotoxic and demonstrated significant antioxidant activity in SH-SY5Y cells exposed to hydrogen peroxide (H₂O₂), highlighting their potential to mitigate oxidative stress: a key pathological factor in Alzheimer’s disease. Structural activity analysis suggests that bromine substitution at position 7 and the presence of a seven-carbon linker are critical for dual ChE inhibition and selectivity towards BChE. ADMET prediction indicates favorable pharmacokinetic properties, including drug-likeness and oral bioavailability. Overall, these findings highlight the potential of the 2-arylbenzofuran as a promising scaffold for multitarget-directed ligands in Alzheimer’s disease therapy. Full article

The widespread use of antibiotics has led to the persistence of antibiotic-resistant bacteria (ARB) and antibiotic resistance genes (ARGs) in drinking water systems, posing potential public health risks at the point of use. In this study, a residential secondary water supply system (SWSS) in eastern China was investigated over one year to characterize microbial communities, ARB and ARG occurrence, and their associations with water quality in bulk water and biofilms. Culture-based methods, flow cytometry, quantitative PCR, and high-throughput 16S rRNA and ITS sequencing were applied. Although conventional treatment removed 94.8% of total bacteria, significant microbial regrowth occurred during secondary distribution, with the highest heterotrophic plate counts observed in rooftop storage tanks (up to 4718 CFU/mL). ARG concentrations increased along the distribution line, and the class 1 integron intI1 was enriched in downstream locations, indicating enhanced horizontal gene transfer potential. Sulfonamide resistance genes dominated the resistome, accounting for more than 60% of total ARG abundance in water samples. Seasonally, ARG levels were higher in autumn and winter, coinciding with elevated disinfectant residuals and lower temperatures. Chlorine was negatively associated with total bacterial abundance, while positive correlations were observed with the relative abundance of several ARGs when normalized to bacterial biomass, suggesting selective pressure under oxidative stress. Turbidity and bacterial abundance were positively correlated with ARB, particularly sulfonamide-resistant bacteria. Biofilms exhibited more stable microbial communities and provided microhabitats that facilitated microbial persistence. Notably, fungal abundance showed strong positive correlations with multiple ARGs, implying that microbial interactions may indirectly contribute to ARG persistence in SWSSs. These findings highlight the role of secondary distribution conditions, disinfectant pressure, and microbial interactions in shaping resistance risks in residential water supply systems, and provide insights for improving microbial risk management at the point of consumption. Full article

The removal of residual free chlorine ions from industrial wastewater is a critical step toward achieving sustainable and environmentally compliant water reuse. Excess chlorine in sludge collector water causes corrosion of process equipment, inhibits biological treatment, and leads to toxic discharge effects. In this study, an intelligent control strategy was developed for an ion-exchange-based dechlorination process to dynamically regulate chlorine concentration in the effluent stream. A pilot-scale ion-exchange filtration unit, designed with a nominal capacity of 500 L h⁻¹, was constructed using a strong-base anion-exchange resin to selectively adsorb chloride and free chlorine ions. A total of 200 experimental observations were obtained to characterize the nonlinear relationship between inlet flow rate and outlet chlorine concentration under varying operational conditions. Based on these experimental data, an Adaptive Neuro-Fuzzy Inference System (ANFIS) model was developed in MATLABR2025 to simulate and control the ion-exchange process. Two model-optimization techniques, Grid Partition + Hybrid and Subtractive Clustering + Hybrid, were applied. The subtractive clustering approach demonstrated faster convergence and superior accuracy, achieving RMSE = 0.147 mg L⁻¹, MAE = 0.101 mg L⁻¹, and R² = 0.993, outperforming the grid-partition model (RMSE ≈ 0.29, R² ≈ 0.97). The resulting ANFIS model was subsequently integrated into a MATLAB/Simulink-based intelligent control system for real-time regulation of chlorine concentration. A comparative dynamic simulation was performed between the proposed ANFIS controller and a conventional PID (Proportional-Differential-Integral) controller. The results revealed that the ANFIS controller achieved a faster response (rise time ≈ 28 s), lower overshoot (≈6%), and shorter settling time (≈90 s) compared to the PID controller (rise time ≈ 35 s, overshoot ≈ 18%, settling time ≈ 120 s). These improvements demonstrate the ability of the proposed model to adapt to nonlinear process behavior and to maintain stable operation under varying flow conditions. Full article

This study systematically assessed the dietary exposure risks of short-chain and medium-chain chlorinated paraffins (SCCPs and MCCPs) through chicken consumption in China, where these persistent organic pollutants are widely produced and used. As an important component of the Chinese diet, chicken was selected as the research matrix due to its high lipid content and potential for chlorinated paraffin bio-accumulation, while available data on these contaminants in market-sold chicken remains limited. We collected 126 representative commercial chicken samples from eight major provinces and municipalities across China and conducted precise analysis using two-dimensional gas chromatography with electron capture negative ionization mass spectrometry (GC×GC-ECNI/MS). The probabilistic exposure assessment was performed through Monte Carlo simulation, and health risks were characterized using the margin of exposure (MOE) approach. The results revealed mean concentrations of 95.8 ng/g wet weight (range: 9.5–1542.4 ng/g ww) for SCCPs and 156.6 ng/g ww (range: 20.0–1517.9 ng/g ww) for MCCPs in chicken samples, with Jiangsu Province exhibiting significantly higher contamination levels compared to other regions (p < 0.001). The estimated mean dietary exposures through chicken consumption were 32.8 ng/kg bw/d for SCCPs and 52.6 ng/kg bw/d for MCCPs in the general Chinese population. Notably, children aged 3–6 years and the Consumer only showed the highest exposure levels. All calculated MOE values substantially exceeded the risk threshold of 1000, indicating no significant health concerns from current exposure to SCCPs and MCCPs through chicken consumption in China. Full article

Photodynamic therapy (PDT) is an established light-based treatment modality that relies on the activation of photosensitizers to generate reactive oxygen species (ROS) and induce localized cytotoxicity. In recent years, microalgae have emerged as a promising and sustainable source of natural photosensitizers due to their ability to biosynthesize structurally diverse pigments with strong light-harvesting capacity. This review provides a comprehensive, application-oriented analysis of microalgae-derived photosensitizers, focusing on chlorophylls and their derivatives, carotenoids, and phycobiliproteins. Particular attention is given to analytical strategies for pigment extraction, purification, and characterization, as well as to photophysical properties, subcellular localization, and ROS-mediated mechanisms underlying photodynamic activity. Recent advances in the chemical modification of algal pigments, including chlorin-based derivatives and 5-aminolevulinic acid–related systems, are critically discussed in relation to structure–activity relationships and translational performance. The accumulated evidence demonstrates that microalgae-derived pigments and their synthetic analogues can achieve efficient singlet oxygen generation, organelle-specific phototoxicity, and favorable therapeutic selectivity. Taken together, these findings highlight microalgae as a renewable and versatile platform for developing next-generation photosensitizers with broad biomedical potential in oncology, dermatology, and antimicrobial photodynamic therapy. Full article