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Microplastics (MPs) in aquatic environments adsorb heavy metals, thereby posing potential environmental risks. However, further research is needed to elucidate the adsorption behavior of different types of MPs for various heavy metals. The aim of this study was to characterize four types of MPs: polypropylene (PP), polyvinyl chloride (PVC), high-density polyethylene (HDPE), and low-density polyethylene (LDPE). Moreover, their Pb 2+ and Cd 2+ adsorption properties were determined to investigate the differences in their capacity to function as heavy metal adsorbents. MPs were characterized via scanning electron microscopy (SEM) using energy dispersive X-ray spectrometer (EDS), Brunauer-Emmett-Teller (BET) analysis, and Fourier transform infrared spectroscopy (FTIR). Adsorption experiment data were analyzed using the Langmuir and Freundlich isotherm models to evaluate the adsorption capacity of the MPs. Based on the results of the adsorption isotherm models and 2D-COS FTIR, the presence of oxygen-containing functional groups, including hydroxyl, carbonyl, and carboxyl groups influences the adsorption process of Pb 2+ and Cd 2+ onto PP and PVC, with the maximum adsorption capacities (Q m ) being 0.759 mg/g and 0.495 mg/g, respectively. Combination of the adsorption isotherm data and characteristics of MPs revealed that the following order of adsorption efficiencies of MPs for each heavy metal: PP > LDPE > PVC > HDPE for Pb 2+ and PP > PVC > LDPE > HDPE for Cd 2+ . The results of this study suggest that MPs, particularly PP and PVC, may serve as vectors for heavy metal transport in aquatic environments, highlighting the need for further research to assess their environmental impact., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Ordered mesoporous aluminum oxide films with porosity ranging between 5% and 37% were synthesized by evaporation-induced self-assembly (EISA) using surfactant templating. To investigate the effects of mesoporous structure on thermal properties, changes in pore structure including pore size, pore distribution, and porosity were monitored as a function of surfactant concentration (Pluronic P-123, poly(ethylene oxide)(20)-poly(propylene oxide)(70)-poly(ethylene oxide)(20)). The ordered mesoporous alumina films were then examined to determine how their morphology influences their thermal properties. These alumina films had a body-centered cubic pore structure or a random-oriented pore structure, depending on the surfactant concentration used, and superior thermal properties were obtained by controlling porosity and pore structure. Therefore, the ordered mesoporous alumina films synthesized in this study can be used as high-temperature thermo-isolating materials., (Copyright 2010 Elsevier Inc. All rights reserved.)

To reduce signal delay in ultra-large-scale integrated circuits, an intermetal dielectric with low dielectric constant is required. Ordered mesoporous silica film is appropriate for use as an intermetal dielectric due to its low dielectric constant and superior mechanical properties. To reduce the dielectric constant, an ordered mesoporous silica film prepared by a tetraethoxysilane/methyltriethoxysilane silica precursor and Brij-76 block copolymer was surface-modified by hexamethyldisilazane (HMDS) treatment. HMDS treatment substituted OH with Si(CH(3))(3) groups on the silica surface. After treatment, ordered mesoporous silica films were calcined at various calcination temperatures, and the calcination temperature to obtain optimal structural, electrical, and mechanical properties was determined to be approximately 300 degrees C.

Organically modified, ordered mesoporous silica films, which can provide hydrophobicity and low polarizability to the framework, were prepared using Brij-76 block copolymer as a template. Due to a fast condensation reaction of the silica precursor, mesostructured silica films were not properly synthesized. To circumvent this problem, a synthesis procedure was modified to provide an enhancement of pore periodicity through the incorporation of methyl ligands on the framework. The micropore volume was reduced, and the pore size was enlarged, as the concentration of the methyl ligands on the framework was increased. A mesophase transition from a two-dimensional hexagonal structure to a body-centered cubic (BCC) structure was observed according to the concentration of incorporated methyl ligands. The mechanical properties of the fabricated films were investigated according to the pore ordering and film density. The mechanical properties of the films with random pore geometry show a positive correlation between film density and elastic modulus. Meanwhile, the mechanical behavior of organically modified mesoporous silica films with periodic pore distribution represents a negative correlation within a certain density range, which is advantageous to the low-k materials. Especially, film with a low micropore volume fraction and BCC pore ordering is more applicable to a low-k material due to low dielectric constant and high mechanical strength.

A new sesquiterpene lactone (1) was isolated with known dihydrochrysanolide derivatives (2 and 3) from the flowers of Chrysanthemum coronarium L., and their structures were identified by spectroscopic data. The stereochemistry of the epimers (1 and 2) was determined from NOESY data and an X-ray crystallographic analysis. The isolated compounds (1-3) were examined for their cytotoxic activity against such human cell lines as A549, PC-3 and HCT-15.