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The ability to tune the surface properties of a polymer film in a simple and effective manner is important for diverse biological, industrial, and environmental applications. In this work, we investigated whether or not the surface free energy of poly(vinyl phenol; PVPh) can be tuned by adjusting the casting solvent and the thermal treatment time, which alters the proportions of intra-and intermolecular hydrogen bonding interactions. Compared to the untreated sample, in tetrahydrofuran (THF) system, the thermal treatment resulted in a lower proportion of intermolecular hydrogen bonds and a concomitant decrease in the surface free energy (from 39.3 to 18.8 mJ/m). In contrast, the thermal treatment in propylene glycol methyl ether acetate (PGMEA) and ethyl-3-ethoxypropionate (EEP) systems increased the proportion of intermolecular hydrogen bonds and the surface free energy of the polymer thin films, from 45.0 to 54.3 mJ/m for PGMEA and from 45.5 to 52.9 mJ/m for EEP. Controlling intermolecular hydrogen-bonding interactions is a unique and easy method for tuning the surface free energies of polymer substances.
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http://dx.doi.org/10.3390/polym12030523 | DOI Listing |
Environ Monit Assess
September 2025
Department of Water Resources Study and Research, Water Research Institute, Tehran, Iran.
Small glaciers situated in high mountainous areas are experiencing notable declines, characterized by unprecedented rates of ice loss in recent years. This study investigates the recent changes in surface elevation and mass loss occurring between 2010 and 2023 within the Alamkouh Glacier over three subperiods, one of the biggest glaciers in Iran and the Middle East. These assessments are derived from a combination of high-resolution LiDAR data in 2010 (with a spatial resolution of 20 cm) and multi-temporal surveys conducted using unmanned aerial vehicles (UAVs) in 2018, 2020, and 2023 (with spatial resolutions varied from 10 to 20 cm).
View Article and Find Full Text PDFDiscov Nano
September 2025
Department of Materials Science and Engineering, National Tsing Hua University, Hsinchu, 30013, Taiwan.
Promoter-assisted chemical vapor deposition (CVD) has emerged as a robust strategy for the low-temperature synthesis of diverse transition metal dichalcogenides (TMDs). In these processes, promoter-induced intermediates facilitate specific reaction pathways, enabling controlled growth via vapor-solid-solid (VSS) or vapor-liquid-solid (VLS) modes. While previous studies have primarily focused on transition metal precursors, growth pathways involving engineered chalcogen-based intermediates remain underexplored due to their volatility and low melting points.
View Article and Find Full Text PDFmSystems
September 2025
Department of Stomatology, Qingdao Women and Children's Hospital Affiliated to Qingdao University, Qingdao, Shandong, China.
Development of dental caries is a dynamic process; yet, there is limited knowledge on microbial differences at various stages of caries at higher resolution. To investigate the shifting microbiome profiles across different caries stages, 30 children were enrolled in this study, including 15 caries-active patients and 15 caries-free individuals. Plaque samples were collected from the buccal surface of caries-free subjects, defined as confident health (CH; = 15).
View Article and Find Full Text PDFSmall
September 2025
Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry, Beijing Normal University, Beijing, 100875, China.
This study presents a novel carbazole derivative functionalized with hydroxy diphosphonic acid groups (HDPACz) as an efficient annealing-free hole transport layer (HTL) through strong bidentate anchoring to indium tin oxide (ITO). Compared to conventional mono-phosphonic acid counterparts, HDPACz demonstrates superior ITO surface coverage and interfacial dipole, effectively modulating the work function of ITO. Theoretical calculations reveal enhanced adsorption energy (-3.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing, 210042, China.
Developing the efficient C─H bond activation carboxylation processes for furoic acid (FA) represents a critical technological challenge in achieving atom-economical synthesis of 2,5-furandicarboxylic acid (FDCA). Despite notable advancements in this field, the inherent contradiction between the high reactivity of furan rings and the chemical inertness of C─H bonds poses substantial technical bottleneck for achieving controllable C─H carboxylation under mild conditions. Herein, we report a high lattice-distorted MnOx catalyst with surface trench-like structures, wherein the Mn-O-conjugated configurations and electron-rich Mn cooperatively drive FA dehydrogenation and carbon radical reduction, inducing the free radical evolution process (FA→carbon-centered FA radical→FA carbanion), then coupled with solvent-polarized CO to accelerate the carboxylation process.
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