When a lithium-ion battery is overcharged, it starts to self-heat because of exothermic reactions occurring within the components of the cell. Separator shutdown is a useful safety feature for preventing thermal runaway reactions in lithium-ion batteries. The polyethylene (PE) separators used here had shutdown temperatures of around 135°C. Because the cell temperature continues to increase before actually beginning to cool even after shutdown, the separator should have a higher meltdown temperature than the shutdown temperature to work as an insulator even above the shutdown temperature. To enhance the meltdown temperature of the separator, in this study, a PE separator was coated with polymers synthesized from various ethylene glycol dimethacrylate monomers. When the separator was coated with polymer synthesized from diethylene glycol dimethacrylate (DEGDMA), its shutdown temperature and meltdown temperature were increased to 142 and 155°C, respectively. Furthermore, a slight increase in the air permeability of the separator was observed when the separator was coated with polymer synthesized from an ethanol solution containing the proper amount of DEGDMA.
Thin-film composite reverse osmosis membranes of polyamides were prepared by interfacial polymerization. Various benzenediamines and poly(aminostyrene) were interfacially reacted with various acyl chlorides to prepare a skin layer of composite membranes. Among the membranes prepared from the structural isomeric monomers of benzenediamines and acyl chlorides, i.e., the same chemical composition but different in the position of functional groups on the aromatic ring, the membrane with the best salt rejection was obtained when the reacting groups forming amide are located at the same position on the aromatic ring. Membranes prepared by interfacially reacting various diamines with trimesoyl chloride revealed that the salt rejection depends on the linear chain structure of polyamides and network formed by crosslinking. Membranes obtained by interfacial polymerization of poly(aminostyrene) with trimesoyl chloride showed higher water flux but lower salt rejection than those obtained by interfacial polymerization of various benzenediamines with trimesoyl chloride. Membranes obtained here showed the typical trade-off behavior between salt rejection and water flux. However, membranes prepared by interfacially reacting trimesoyl chloride with a mixture of poly(aminostyrene) and m-phenylenediamine or a mixture of poly(aminostyrene), m-phenylenediamine, and diaminobenzoic acid showed a performance advantage over usual membranes, i.e., a large positive deviation from the usual trade-off trend.
Nitrogen-doped nano-onions (NNO) were prepared as electrocatalytic materials for the oxygen reduction reaction (ORR). The nano-onions (NO), spherical graphitic material particles, were prepared by pyrolysis of nanodiamonds (ND). Oxidized NO (ONO) was prepared from NO by a modified Hummers’ method, and this was mixed with urea, followed by pyrolysis, resulting in the formation of NNO. The nitrogen content and molar ratio of nitrogen-containing groups in the NNOs were varied by controlling the oxygen content of ONO to explore the effect of nitrogen content on the ORR activity. The formation of NO was confirmed by Raman spectroscopy, X-ray diffraction analysis, and high-resolution transmission electron microscopy. X-ray photoelectron spectroscopy analyses were conducted to confirm the formation of the NNO and the structures of the nitrogen-containing groups in the NNOs. The ORR activities of the NNOs were investigated using a rotating disk electrode. The NNOs showed a higher onset potential than that of NO, and the ORR activity of the NNO could be improved by increasing the number of active sites (nitrogen-containing groups) in the NNO. In addition, the NNO exhibited better long-term stability and resistance toward methanol crossover in the ORR than the platinum-based catalysts.
The applications of dental restorative composite resins containing 2,2 bis [4-(2-hydroxy-3-methacryloyloxy propoxy) phenyl] propane (Bis-GMA), as a base resin, and triethylene glycol dimethacrylate (TEGDMA), as a diluent, are often limited in dentistry due to the relatively large amount of volumetric shrinkage that occurs during the curing reaction. In this study, various new resin matrices were examined for use as dental composites in order to reduce the amount of volumetric shrinkage that occurs in dental composites as a result of curing. Bis-GMA derivatives were synthesized by substituting methyl groups for hydrogen on the phenyl ring. The derivatives of TEGDMA with different chain lengths or reactive groups were also examined. The molecular structural changes in the TEGDMA derivatives were not effective in reducing the level of volumetric shrinkage. The resin matrix containing a Bis-GMA derivative and TEGDMA showed a reduced amount of volumetric shrinkage in proportion to the number of methyl groups on the phenyl rings. Polymerization with a mixture of Bis-GMA, its derivatives and a diluent is a promising strategy for obtaining a polymer with a low amount of volumetric shrinkage. A comparison of the volumetric shrinkage of dental composites containing Bis-GMA, TMBis-GMA (2,2-bis[3,5-dimethyl, 4-(2-hydroxy-3-methacryloyloxy propoxy) phenyl] propane)), and TEGDMA with that prepared from a Bis-GMA and TEGDMA mixture showed that the volumetric shrinkage reduction in the new resin was approximately 50%. Furthermore, the mechanical strength of the former was higher than that of the latter.
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