Sunjong Lee

Ultra-high-molecular-weight polyethylene membranes are promising materials for semiconductors, medical, and separation processes due to their high chemical resistance and mechanical robustness. However, their inherently low surface energy and chemical inertness impose substantial limitations on surface functionalization and water permeation. In this study, we propose a strategy to introduce an ethylenediaminetetraacetic acid chelating layer by integrating a hydrophilic interlayer formed through tannic acid–3-aminopropyltriethoxysilane coating with a photoacid-induced sol–gel reaction. This approach overcomes the constraints of conventional membranes and enables effective removal of trace metal ions. The optimized membrane (A10T50) exhibits a mean pore diameter of 81.4 nm and maintains a high water flux of 1881 L·m−2·h−1 while achieving approximately 95% Cu(II) removal, corresponding to an adsorption capacity of 1.4 × 10−4 meq·cm−2. Furthermore, the regenerated membranes consistently maintained more than 90% removal efficiency across multiple cycles, while preserving the average area-specific adsorption capacities of 4.39 × 10−4 meq·cm−2 (Al(III)), 2.15 × 10−4 meq·cm−2 (Ni(II)), 1.87 × 10−4 meq·cm−2 (Zn(II)), and 1.45 × 10−4 meq·cm−2 (Cu(II)). These findings demonstrate that photoacid-mediated silanization offers a controllable and scalable route to fabricate metal-ion-chelating ultra-high-molecular-weight polyethylene membranes suitable for ultrapure water polishing applications.

Currently, polypropylene (PP) is used in various products, thus leading to high daily exposure in humans. Thus, it is necessary to evaluate the toxicological effects, biodistribution, and accumulation of PP microplastics in the human body. In this study, administration of two particle sizes of PP microplastics (approximately 5 and 10–50 µm) did not lead to any significant changes in several toxicological evaluation parameters, including body weight and pathological examination, compared with the control group in ICR mice. Therefore, the approximate lethal dose and no-observed-adverse-effect level of PP microplastics in ICR mice were established as ≥2000 mg/kg. Furthermore, we manufactured cyanine 5.5 carboxylic acid (Cy5.5-COOH)-labeled fragmented PP microplastics to monitor real-time in vivo biodistribution. After oral administration of the Cy5.5-COOH-labeled microplastics to the mice, most of the PP microplastics were detected in the gastrointestinal tract and observed to be out of the body after 24 h in IVIS Spectrum CT. Therefore, this study provides a new insight into the short-term toxicity, distribution, and accumulation of PP microplastics in mammals.

The increased use of plastics has led to severe environmental pollution, particularly by microplastics—plastic particles 5 mm or less in diameter. These particles are formed by environmental factors such as weathering and ultraviolet irradiation, thereby making environmental pollution worse. This environmental pollution intensifies human exposure to microplastics via food chains. Despite potential negative effects, few toxicity assessments on microplastics are available. In this study, two sizes of polytetrafluoroethylene (PTFE) microplastics, approximately 5 μm and 10–50 μm, were manufactured and used for single and four-week repeated toxicity and pharmacokinetic studies. Toxicological effects were comprehensively evaluated with clinical signs, body weight, food and water consumption, necropsy findings, and histopathological and clinical-pathological examinations. Blood collected at 15, 30 60, and 120 min after a single administration of microplastics were analyzed by Raman spectroscopy. In the toxicity evaluation of single and four-week repeated oral administration of PTFE microplastics, no toxic changes were observed. Therefore, the lethal dose 50 (LD₅₀) and no-observed-adverse-effect-level (NOAEL) of PTFE microplastics in ICR mice were established as 2000 mg/kg or more. PTFE microplastics were not detected in blood, so pharmacokinetic parameters could not be calculated. This study provides new insight into the long-term toxicity and pharmacokinetics of PTFE microplastics.

The production, use, and waste of plastics increased worldwide, which resulted in environmental pollution and a growing public health problem. In particular, microplastics have the potential to accumulate in humans and mammals through the food chain. However, the toxicity of microplastics is not well understood. In this study, we investigated the toxicity of 10–50 μm polyethylene microplastics following single- and 28-day repeated oral administration (three different doses of microplastics of 500, 1000, and 2000 mg/kg/day) in ICR mice. For the investigation, we administered the microplastics orally for single- and 28-day repeated. Then, the histological and clinical pathology evaluations of the rodents were performed to evaluation of the toxicity test, and Raman spectroscopy was used to directly confirm the presence of polyethylene microplastics. In the single oral dose toxicity experiments, there were no changes in body weight and necropsy of the microplastics-treated group compared with that of controls. However, a histopathological evaluation revealed that inflammation from foreign bodies was evident in the lung tissue from the 28-day repeated oral dose toxicity group. Moreover, polyethylene microplastics were detected in the lung, stomach, duodenum, ileum, and serum by Raman spectroscopy. Our results corroborated the findings of lung inflammation after repeated oral administration of polyethylene microplastics. This study provides evidence of microplastic-induced toxicity following repeated exposure to mice.

Polymer foams are used in everyday life for industrial and household applications. However, the time‐releasing ammonia is environmentally harmful that becomes attractive. Here, we introduce a technically advanced synthetic process for the polyvinyl chloride (PVC) foam, in which the emission of ammonia gas is significantly reduced by using the polymeric acids. The PVC foam has processed with azodicarbonamide (ADCA) as a chemical blowing agent after the solid type polymeric acid is mixed as supporting agent. While the characteristic properties such as specific gravity (density) and chromaticity of PVC foams are not critically changed, the reduction of time‐releasing ammonia is up to 85% compared to the PVC foam without polymeric acid. This is attributed to the cell structure with small sub‐cells and lots of connecting channels and the chemically capturing ammonia of polymeric acids.

Self-healing, an autonomous repairing process stimulated by damage, has recently attracted a great deal of attention in the field of medical and mechanical engineering as well as from scientists, due to its valuable potential applications. However, as the self-healing process is mediated by specific functional materials, practical applications have been limited. Here, we introduce a healable homopolymer microcapsule that can self-heal a crack or cleaved part through a photochemical [2 + 2] cycloaddition process. Microcapsules were prepared through photopolymerization and suspension polymerization, each containing 1,1,1-tris (cinnamoyloxymethyl) ethane (TCE) and 1,1-di (cinnamoyloxymethyl) ethane (DCE) monomers, which act as healing materials. TCE and DCE monomers were polymerized into poly (TCE-co-DCE) without a photoinitiator under illumination. The epoxy specimen embedded with microcapsules showed obvious healing performance during illumination after cracking. From the FT-IR spectra for each step of the healing process, the specimen could be repeatedly self-healed through the reversible process of cyclobutane cross-links to the original cinnamate and vice versa. This work shows an alternative approach using homopolymer microcapsules to accomplish the repeatable self-healing of a crack without interface discontinuity, which could be adopted as a healing substance in various paints.

Development of eco-friendly polymer foams is an urgent research topic because of the serious environmental pollution caused by trash heaps and the time-release of harmful gases. Polymer PVC foam using azodicarbonamide as a chemical foaming agent has been highly requested for further improvement due to the residual ammonia gas that continuously leaks out. Here, we demonstrate an effective and costless process for the reduction of releasing ammonia from PVC foams using the overcoat technology of deodorants. We have selected four candidate materials, gelite, zeolite, terra alba, and fumed silica as original materials for the deodorant of ammonia, and they showed an ammonia deodorization rate (ADR) of over 80% without any treatment except the fumed silica. When we over-coated the UV-curing agent mixed deodorants on the PVC foams (thickness ~300 µm), the ADR of the terra alba and zeolite complex foams was remarkably higher than 90%, however, the specific gravity and chromaticity were not changed within 20%. This indicates that our developed process using deodorant layer for ammonia reduction has a high potential for the production of eco-friendly polymer foams.

Recently, the light-matter interaction at nanoscale has attracted great interest from physicists, chemists and material scientists, as it gives peculiar optical properties that couldn’t be observed at the bulk scale. The synthesis and characterization of organic-inorganic heterostructures forming quantum dots, nanowires or nanotubes provide opportunities to understand their photophysical mechanism and to apply optoelecronic devices. Herein, we report a huge enhanced luminescence in a coaxial-like heterostructured poly (3-methylthiophene) (P3MT) with Au. We electrochemically synthesized P3MT nanowires (NWs) on a nanoporous template, and sequentially deposited Au on the surface of P3MT NWs. The diameter of heterostructured P3MT/Au NWs was about 200 nm, where the cladding-shape Au were about 10 nm. The visible range absorbance, with two new absorption peaks of P3MT/Au NWs, was significantly increased compared with that of P3MT NWs. Accordingly, the photoluminescence (PL) of a P3MT/Au NW was enormously increased; up to 170 times compared to that of P3MT NWs. More interestingly, an unexpected enhancement of PL was observed from cross-junction point of P3MT/Au NWs. The abnormal PL properties of P3MT/Au NWs were attributed to the charge transfer and the surface plasmon resonance between the cladding-shape Au and the core-shape P3MT, which resulted in the enhanced quantum yield. This incites us to reconsider the light-matter interaction in polymer-metal hybrid structures applicable for high-performance optoelectronic devices.