Search Results (240)

This study investigates the antioxidant, antimicrobial, and antitumor activities of Taraxacum officinale (Dandelion) and Artemisia annua (Sweet Wormwood) extracts, along with their role in the green synthesis of gold (AuNPs) and silver nanoparticles (AgNPs). Bioreduction was achieved using aqueous and ethanolic extracts (100 mg/mL), enabling solvent-dependent comparisons. Nanoparticles were characterized using ultraviolet–visible spectroscopy (UV–Vis), fluorescence spectroscopy, scanning electron microscopy (SEM), dynamic light scattering (DLS), high-resolution transmission electron microscopy (HRTEM), and zeta potential analysis. Each technique revealed complementary aspects of nanoparticle morphology, size, and stability, with UV–Vis indicating aggregation states and DLS confirming solvent-related size variation even at 3–5% ethanol. Gold nanoparticles synthesized from Dandelion showed strong antibacterial activity against Staphylococcus aureus, while silver nanoparticles from both plants were effective against Escherichia coli. Cytotoxicity assays indicated that silver nanoparticles obtained from ethanolic Dandelion extract containing 3% ethanol in aqueous solution (AgNPsE_ETOH3%-D) significantly reduced LoVo (p = 4.58 × 10⁻³) and MDA-MB-231 (p = 7.20 × 10⁻⁵) cell viability, with high selectivity indices (SI), suggesting low toxicity toward normal cells. Gold nanoparticles synthesized from aqueous Dandelion extract (AuNPsEaq-D) also showed favorable SI values (2.16 for LoVo and 8.41 for MDA-MB-231). Although some formulations demonstrated lower selectivity (SI < 1.5), the findings support the therapeutic potential of these biogenic nanoparticles. Further in vivo studies and pharmacokinetic evaluations are required to validate their clinical applicability. Full article

Recent studies have increasingly focused on molecular interactions between small molecules and proteins, especially binding mechanisms and thermodynamics, using multispectroscopic and molecular dynamics approaches. This study elucidated the molecular interaction mechanism between bovine serum albumin (BSA) and trans-resveratrol (Res) through an integrated approach combining multispectroscopic analyses and molecular dynamics simulations. The fluorescence quenching study revealed a static quenching mechanism between BSA and Res, which was further confirmed via ultraviolet–visible (UV-Vis) absorption spectroscopy. In particular, K_SV decreased from 5.01 × 10⁴ M⁻¹ at 298 K to 3.99 × 10⁴ M⁻¹ at 318 K. Furthermore, the calculated K_q values significantly exceeded 1 × 10¹² M⁻¹ s⁻¹. With increasing Res concentration, the peak fluorescence intensities of Tyr and Trp residues both exhibited a blue shift. The α-helix content of the BSA–Res complex was 59.8%, slightly lower than that of BSA (61.3%). Res was found to bind to site I in subdomain IIA of BSA. The molecular dynamics simulation also identified the specific binding of Res to site I of BSA, while thermodynamic studies revealed that the binding process occurs spontaneously and is primarily mediated by hydrogen bonding interactions. These findings not only enrich the theoretical framework of small-molecule–protein interactions but also provide a crucial scientific foundation for the development and utilization of natural products. Full article

This paper presents the synthesis of La₂Ti₂O₇ nanoparticles by the sol–gel method starting from lanthanum nitrate and titanium alkoxide (noted as LTA). Subsequently, the lanthanum titanium oxide nanoparticles are modified with noble metals (platinum) using the chemical impregnation method, followed by a reduction process with NaBH₄. The comparative analysis of the structure and surface characteristics of the nanopowders subjected to thermal treatment at 900 °C is conducted using Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray fluorescence (XRF), ultraviolet-visible (UV–Vis) spectroscopy, as well as specific surface area and porosity measurements. The photocatalytic activity is evaluated in the oxidative photodegradation of ethanol (CH₃CH₂OH) under simulated solar irradiation. The modified sample shows higher specific surfaces areas and improved photocatalytic properties, proving the better conversion of CH₃CH₂OH than the pure sample. The highest conversion of ethanol (29.75%) is obtained in the case of LTA-Pt after 3 h of simulated solar light irradiation. Full article

This study aimed to develop polylactic acid (PLA)-based membranes incorporating tramadol (TMD) using air jet spinning (AJS), ensuring stable physicochemical properties and biocompatibility. Two groups were fabricated: 10% PLA membranes (control) and 10% PLA membranes loaded with TMD in an 80:1 ratio (experimental). Characterization included scanning electron microscopy (SEM), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FT-IR), ultraviolet-visible spectroscopy (UV-VIS), and biocompatibility assays with human osteoblasts using resazurin, crystal violet staining, and 5-chloromethylfluorescein diacetate for fluorescence microscopy. SEM revealed a homogeneous, randomly distributed fiber pattern, with diameters under 5 µm and no structural voids. DSC and TGA indicated that TMD was uniformly incorporated, increased the thermal capacity, and slightly lowered the onset and inflection degradation temperatures. FT-IR confirmed the chemical compatibility of TMD with PLA, showing no structural alterations. UV-VIS detected sustained TMD release over 72 h. Biocompatibility tests showed no cytotoxic effects; cell viability and proliferation in TMD-loaded membranes were comparable to controls. Statistical analysis used ANOVA and Wilcoxon tests. 10% PLA membranes loaded with TMD at an 80:1 ratio exhibited stable physicochemical characteristics and favorable biocompatibility, supporting their potential use in drug delivery systems. Full article

This study systematically investigates for the first time the effects of dual-site co-cultivation on spectral characteristics and trace element enrichment in marine-cultured Akoya pearls from Beihai, China. Akoya pearls were cultured over a one-year period, with the final 40-day stage designated as the terminal phase. During this period, two experimental groups of pearl oysters were established: Group Y remained in Beihai for continued local cultivation and harvest, while Group B was transferred to Weihai, Shandong Province, for terminal-stage farming under different thermal conditions. A series of comparative analyses were performed using Fourier-transform infrared (FTIR) spectroscopy, ultraviolet-visible (UV-Vis) spectroscopy, Raman spectroscopy, X-ray fluorescence (XRF), and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The FTIR results revealed distinct differences between the two groups in the distribution of amide and polysaccharide functional groups, particularly around 1643 cm⁻¹ and 1100 cm⁻¹. The UV-Vis spectra of Group B displayed characteristic absorption bands at 430 nm and 460 nm, associated with the organic matrix of the nacre. Raman spectroscopy further indicated a higher abundance of organic-related vibrational features in Group B. Additionally, both XRF and LA-ICP-MS analyses consistently showed significant differences in the concentrations and distributions of trace elements, particularly copper (Cu), cobalt (Co), and zinc (Zn). The findings demonstrate that the dual-site co-cultivation mode significantly impacts both the organic composition and trace element enrichment patterns in seawater Akoya pearls. This research provides valuable references for optimizing environmental parameters in pearl cultivation processes. Full article

Rainwater needs to be recognized as a natural water source for domestic use, but finding viable processes to remove its contaminants is essential. The aim of this work was to compare the UV/H₂O₂ and UV/Fenton-like processes for the oxidation of 3,5-dihydroxybenzoic acid (3,5-DHBA) in rainwater. The reactions were assessed using ultraviolet-visible (UV-Vis) and molecular fluorescence spectroscopies, and the results showed the formation of new and similar chromophoric compounds in both processes, which were subsequently degraded. At environmentally relevant concentrations of chemical oxidants, namely H₂O₂ at 10⁻⁴ M, the chromophoric organic compounds in solution were degraded within 24 h by the UV/H₂O₂ process and within 4 h by the UV/Fenton-like process. However, when the concentration of H₂O₂ was increased by one order of magnitude for the UV/H₂O₂ process (from 10⁻⁴ M to 10⁻³ M), oxidation rates were similar and nearly complete after 4 h for both UV/H₂O₂ and UV/Fenton-like processes. These findings highlight that the presence of more oxidizing agents in the oxidation system improves the synergistic effect, leading to a greater contribution of the free radical oxidation pathway, particularly through hydroxyl radicals. Thus, by increasing the concentration of H₂O₂ in the UV/H₂O₂ process to 10⁻³ M, it was possible to achieve a similar level of oxidation (close to 100% after 4 h, as indicated by a decrease in fluorescence intensity) as the UV/Fenton-like process at environmentally relevant concentrations (10⁻⁴ M), but using fewer chemical reactants, since UV/H₂O₂ process does not require Fe(III) as catalyst and oxidant. Therefore, the UV/H₂O₂ process can be considered a simpler and cleaner process for removing organic contaminants from rainwater. Full article

This study employs a plasma-coupled calcium peroxide (CaO₂) system to degrade tetracycline (TC) and remove phosphorus from emergency wastewater in a chemical industry park. The plasma/CaO₂ system achieves optimal performance when the CaO₂ dosage reaches 0.13 g/L. Higher degradation efficiencies of TC were observed at increased discharge voltages, frequencies, and under weakly acidic and weakly alkaline conditions. Variations in discharge voltage and frequency have no significant impact on the phosphorus removal efficiency, but weakly alkaline conditions favor phosphorus removal. The reactive species (·OH, ¹O₂, O₂·⁻) within the plasma/CaO₂ system were identified, and their roles were elucidated using radical scavengers. Subsequently, the degradation process was characterized by measuring changes in total organic carbon (TOC), chemical oxygen demand (COD), and ammonia nitrogen during the reaction, along with three-dimensional fluorescence analysis and ultraviolet-visible spectroscopy (UV-Vis). Eight intermediate products were identified through LC-MS, and two degradation pathways were clarified based on density functional theory. The toxicity analysis of the intermediate products demonstrated that the plasma/CaO₂ system is an efficient, feasible, and environmentally friendly method for the synchronous removal of organic pollutants and phosphorus from emergency wastewater in a chemical industry park. Full article

Background: Breast cancer and chronic bacterial infections are pressing global health issues, and traditional treatments are often hampered by resistance and adverse side effects. This study sought to create silver nanoparticles (AgNPs) through eco-friendly synthesis using Hibiscus rosa sinensis (HRS) flower extract and to assess their antibacterial, antibiofilm, and anticancer properties. Methods: HRS extract functioned as both a reducing and stabilizing agent in the synthesis of AgNPs. The nanoparticles were characterized using ultraviolet–visible spectroscopy (UV–Vis), Fourier-transform infrared (FTIR) spectroscopy, and transmission electron microscopy (TEM). Antibacterial and antibiofilm properties were evaluated against gram-positive (Staphylococcus aureus and Enterococcus faecalis) and gram-negative (Escherichia coli and Pseudomonas aeruginosa) bacteria using agar well diffusion and XTT reduction assays. The cytotoxic effects on MDMB-231 breast cancer cells and normal splenocytes were measured using the MTT assay, whereas fluorescence microscopy was used to observe reactive oxygen species (ROS) production, changes in mitochondrial membrane potential, and caspase-3 activation. Results: The synthesized HRS-AgNPs, primarily ranging from 10 to 50 nm, displayed a distinct surface plasmon resonance (SPR) peak at 428 nm. They exhibit notable antibacterial activity, especially against gram-positive bacteria, and effectively disrupt bacterial biofilms. Cytotoxicity evaluations showed that HRS-AgNPs decreased the viability of MDMB-231 cells in a dose-dependent manner, with minimal toxicity observed in normal splenocytes. The increase in ROS levels, reduction in mitochondrial membrane potential, and heightened caspase-3 activity collectively suggest apoptosis-driven cell death in cancer cells. Conclusions: HRS-AgNPs demonstrated dual functionality, with strong antibacterial and selective anticancer effects. Their environmentally friendly synthesis, stability, and significant biological activities suggest their potential for further development, including in vivo safety and efficacy assessments for clinical applications in treating infections and breast cancer. Full article

Organic violet-blue fluorescent materials have garnered significant interest for a broad spectrum of applications. A series of triazine-based molecules, that is, 2,4,6-tri(9H-carbazol-9-yl)-1,3,5-triazine (TCZT), 2,4,6-tri(1H-indol-1-yl)-1,3,5-triazine (TIDT), and 2,4,6-tris(3,6-di-tert-butyl-9H-carbazol-9-yl)-1,3,5-triazine (TDBCZT), exhibiting violet-blue emission were synthesized via a catalyst-free aromatic nucleophilic substitution reaction. These compounds possess a non-planar and twisted structure with favorable charge-transfer characteristics, demonstrating excellent thermal stability (decomposition temperatures of 370 °C, 384 °C, and 230 °C, respectively). Cyclic voltammetry analysis, combined with time-dependent density functional theory (TD-DFT) calculations at the B3LYP/6-31G(d) level, offered detailed insights into their electronic structures and electrochemical properties. Optical properties were systematically characterized using Ultraviolet–visible (UV–Vis) absorption and photoluminescence (PL) spectroscopy. The compounds exhibited violet-blue luminescence with emission peaks located at 397 nm, 383 nm, and 402 nm in toluene, respectively. In their respective films, the compounds exhibited varying degrees of spectral shifts, with emission peaks at 408 nm, 381 nm, and 369 nm. Moreover, the CIE (Commission Internationale de l’Éclairage) coordinates of TIDT in toluene were (0.155, 0.067), indicative of excellent violet purity. These compounds demonstrated significant two-photon absorption (TPA) properties, with cross-sections of 4.6 GM, 15.3 GM, and 7.4 GM, respectively. Notably, they exhibited large molar absorptivities and substantial photoluminescence quantum yields (PLQYs), suggesting their potential for practical applications as violet-blue fluorescent materials. Full article

The Autler–Townes (AT) doublet, a fundamental manifestation of quantum interference effects, serves as a critical tool for studying the dynamic behavior of Rydberg atoms. Here, we investigate the asymmetry of the Autler–Townes (AT) doublet in the trap-loss fluorescence spectroscopy (TLFS) of cesium (Cs) atoms confined in a magneto-optical trap (MOT) with single-step Rydberg excitation using a 319-nm ultraviolet (UV) laser. A V-type three-level system involving the ground state $6{\mathrm{S}}_{1/2}$ (F = 4), excited state $6{\mathrm{P}}_{3/2}$ (${\mathrm{F}}^{\prime }$ = 5), and Rydberg state ($n{\mathrm{P}}_{3/2}$ (${\mathrm{m}}_{\mathrm{J}}$ = +3/2)) is theoretically modeled to analyze the nonlinear dependence of the AT doublet’s asymmetry and interval on the cooling laser’s detuning. Experiments reveal that as the cooling laser detuning ${\mathsf{\Delta }}_1$ decreases from −15 MHz to −10 MHz, the AT doublet exhibits increasing symmetry, while its interval shows a nonlinear decrease. Theoretical simulations based on the density matrix equation and Lindblad master equation align closely with experimental data, confirming the model’s validity. This study provides insights into quantum interference dynamics in multi-level systems and offers a systematic approach for optimizing precision measurements in cold atom spectroscopy. Full article

Styrene-butadiene-styrene (SBS)-modified asphalt, a widely utilised binder in pavement engineering, is susceptible to ageing due to the coupling effects of thermo-oxidation, ultraviolet radiation, and humidness. Due to the limited availability of high-quality asphalt resources, recycling aged asphalt has emerged as a vital strategy for addressing resource shortages and reducing environmental pollution. This study investigated the effects of thermal-ultraviolet-humidness coupled ageing on the pavement performance of SBS-modified asphalt, with a specific focus on the hot–wet climates of Guangzhou and Chengdu. Beijing’s standard climate serves as a reference for this study. Additionally, industrial animal oil was chosen as a rejuvenator for aged SBS-modified asphalt. The mechanisms underlying hot–wet coupling ageing and regeneration of SBS-modified asphalt were analysed using Fourier Transform Infrared Spectroscopy (FTIR) and Fluorescence Microscopy (FM). The findings indicate that thermal-oxidation and humidness accelerate sulphide formation, resulting in a marked increase in sulfoxide groups and facilitating the migration of lighter components, ultimately leading to asphalt hardening. Under high-temperature and humidness conditions, the butadiene index (BI) of asphalt decreased by 5.96% in Chengdu and 15.78% in Guangzhou compared to Beijing. The sulfoxide index (SI) and aromaticity index (CI) increased by 3.74% and 3.89% in Chengdu, and by 9.39% and 8.54% in Guangzhou, respectively, confirming the exacerbating effect of humidness on ageing. During the regeneration process, industrial animal oil effectively diluted polar molecules in aged asphalt, resulting in reductions in SI by 38.88%, 36.74%, and 37.74%, and in CI by 63.77%, 62.54%, and 63.11% under ageing conditions in Beijing, Guangzhou, and Chengdu, respectively. Rejuvenation is achieved by replenishing lighter components, thereby promoting the aggregation and swelling of the degraded SBS chains. Full article

The polymorphism of the ultraviolet luminescent security ink Orlyum White 520T (N-(2-(4-oxo-4H-benzo[d][3,1]-oxazin-2-yl)phenyl)naphthalene-2-sulfonamide) is revealed, obtaining two new polymorphic forms with enhanced stability. Beyond the known form (lit. mp. 184.8–185.2 °C, Form III, YOCTAO), we succeeded in gaining two new polymorphic forms, Form II and Form I, with higher melting points of 195–196 and 197–198 °C, respectively. Their elemental composition, ¹H and ¹³C NMR spectra have been found to be identical, while their powder XRD patterns and FT-IR spectra are significantly different. Based on the single-crystal structure determination of Form II and redetermination of Form III, we uncover the similarities and differences in their packing arrangement and in their secondary interaction systems, all of which affect the molecular conformations in their crystals. In order to explain their significantly distinguishable melting points, Hirshfeld surface analysis and lattice energy calculations have also been carried out. We have made efforts toward revealing the reproducible conditions under which certain polymorphs are formed. It seems that the solvents or other probable organic contaminations are more likely responsible for the formation, nucleation and growth of crystals of various polymorphic forms, traced by thermogravimetric evolved gas analysis (TG/DTA-EGA-MS). Full article

The alpine peatlands in western Sichuan Province are currently experiencing aridification. To understand the effects of aridification on the characteristics of organic carbon release from alpine soils, the soil in the northwest Sichuan Plateau was investigated. Soil columns were incubated under different moisture conditions in situ and in the laboratory, and ultraviolet-visible absorption spectroscopy and three-dimensional fluorescence spectroscopy were used to assess the soil dissolved organic carbon (DOC) levels. The results revealed that (1) the cumulative release of DOC from alpine soil in the northwest Sichuan Plateau decreased with decreasing moisture content. The cumulative release of soil DOC in the laboratory (0–5 cm soil reached 1.93 ± 0.43 g/kg) was greater than that from soil incubated in situ (0–5 cm soil reached 1.40 ± 0.13 g/kg); (2) the cumulative release of DOC in 0–5 cm soil exhibited the greatest response to changes in water content, and the cumulative release of DOC from the 0–5 cm soil layer (1.40 ± 0.13 g/kg) was greater than that from the 5–15 cm soil layer (1.25 ± 0.03 g/kg); and (3) UV-visible absorption spectra and 3D fluorescence spectral characteristics indicated that aridification increases the content of chromophoric dissolved organic matter (CDOM) components with strong hydrophobicity, especially tyrosine components (surface soil increased 39.59~63.31%), in alpine soil DOC. This increase in hydrophobic CDOM components enhances the aromaticity and degree of humification of DOC. Our results revealed that drought inhibits the release of soil DOC, which is unfavorable for the sequestration of organic carbon in alpine soils, potentially resulting in the loss of soil carbon pools and further degradation of alpine ecosystem functions. Full article

This study investigated key factors in the petrochemical industry and evaluated the oxidation performance of ozonation catalytic oxidation for treating phenol-simulated wastewater and actual wastewater spiked with phenol. In simulated phenol wastewater, optimal conditions (ozone dosage of 8 mg/L/min, pH 11, total dissolved solids (TDSs) of 1000 mg/L, and initial phenol concentration of 50 mg/L) yielded a maximum chemical oxygen demand (COD) removal rate of 90.60%. For actual wastewater spiked with phenol under the same conditions, maximum removal rates of phenol, COD, and total organic carbon (TOC) were 65.45%, 63.57%, and 79.65%, respectively. The degradation mechanisms and changes in organic matter during ozonation were analyzed using three-dimensional fluorescence spectroscopy, ultraviolet spectroscopy, and gas chromatography–mass spectrometry (GC-MS). The findings demonstrate that ozonation oxidation is an effective wastewater treatment method, significantly reducing pollutant concentrations and enhancing water quality. Full article

Organic semiconductor materials are interesting due to their application in various organic electronics devices. [1]benzothieno[3,2-b][1]benzothiophene (BTBT) is a widely used building block for the creation of such materials. In this work, three novel solution-processable regioisomeric derivatives of BTBT—2,7-bis(3-octylthiophene-2-yl)BTBT (1), 2,7-bis(4-octylthiophene-2-yl)BTBT (2), and 2,7-bis(5-octylthiophene-2-yl)BTBT (3)—were synthesized and investigated. Their optoelectronic properties were characterized experimentally by ultraviolet–visible and fluorescence spectroscopy, time-resolved fluorimetry, and cyclic voltammetry and studied theoretically by Time-Dependent Density Functional Theory calculations. Their thermal properties were investigated by a thermogravimetric analysis, differential scanning calorimetry, polarizing optical microscopy, and in situ small-/wide-angle X-ray scattering measurements. It was shown that the introduction of alkyl substituents at different positions (3, 4, or 5) of thiophene moieties attached to a BTBT fragment significantly influences the optoelectronic properties, thermal stability, and phase behavior of the materials. Thin films of each compound were obtained by drop-casting, spin-coating and doctor blade techniques and used as active layers for organic field-effect transistors. All the OFETs exhibited p-channel characteristics under ambient conditions, while compound 3 showed the best electrical performance with a charge carrier mobility up to 1.1 cm²·V⁻¹s⁻¹ and current on/off ratio above 10⁷. Full article