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11.
锂离子电池(LIB)是日常生活中最常见的便携式储能设备。然而,传统的锂离子电池多使用液态电解质(LE),存在易泄漏、易燃易爆且有毒等危险,其安全性日益受到关注。与LE相比,凝胶聚合物电解质(GPE)安全性更好且其电化学性能最接近LE,成为近年来电解质方面的研究重点。本文综述了近年来国内外GPE在LIB方面的研究进展,总结了传统聚合物基质采用交联、共聚或共混改性以提高电解质电化学性能及改善安全性方面的研究,并介绍了可再生、可降解的高分子材料在LIB方面的应用,旨在为研究功能性更强的GPE及高性能电极材料的研究提供参考。 相似文献
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In this article, isocyanate was adopted to modify Y2O3 powder for the purpose of preparing transparent Y2O3 ceramics via gel casting. The modification could enhance the hydration resistance of Y2O3 powder through the steric hindrance effect. The coating mechanism can be proved by the infrared spectrum of the surface-modified Y2O3 powder. Modification could not only prevent Y2O3 particles from reacting with water, but also prevents agglomeration between particles. The viscosity of the slurry with a solid content of 52.7 vol% is only 0.48 Pa·s at the shear rate of 100 s−1, which is suitable for preparing high-density compacts by gel casting. The transmittance of the sample (1840°C × 8 h, 1 mm thickness) at 1100 nm reaches 75%. The microstructure of the sintered body is dense with the average grain size of 6.5 μm without obvious impurities nor pores. Five mol% ZrO2-doped Y2O3 transparent ceramic fairing with the diameter of 5 cm without defects was successfully fabricated by gel casting (52.7 vol% solid volume) and vacuum sintering (1840°C × 8 h). 相似文献
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Irshad Ahmad Shazia Shukrullah Muhammad Yasin Naz Muhammad Athar Rasheed Mukhtar Ahmad Ejaz Ahmed Muhammad Shoaib Akhtar N.R. Khalid Abid Hussain Sadia Khalid 《International Journal of Hydrogen Energy》2021,46(53):26711-26724
CNTs were decorated onto Sr doped ZnO nanoparticles to construct an efficient photocatalyst via a facile sol-gel method. The as-fabricated Sr doped ZnO/CNTs with recyclability exhibits Sr and CNTs content dependent hydrogen evolution activit under visible light illumination. The Sr doped ZnO/CNTs photocatalyst shows the highest hydrogen evolution rate of 2732.2 μmolh?1g?1, which is 33.7 and 2.83 times higher than pure ZnO and Sr doped ZnO photocatalysts, respectively. The improved hydrogen evolution activity of Sr doped ZnO/CNTs is primarily assigned to high surface area, Sr doping and construction of heterojunction, which can extend the light absorption, decrease the optical band gap and improve the charge separation. Moreover, the underlying photocatalytic mechanism is proposed on the basis of Mott-Schottky study and explains the interfacial charge transfer process from ZnO to CNTs and Sr. This work open new strategies to synthesize CNTs based nanocomposite for hydrogen evolution. 相似文献
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《Ceramics International》2021,47(24):34836-34844
Bone defects accompanied by infection or inflammation can significantly delay the healing process. To simultaneously achieve controlled release of local antibiotics for infection control and bone healing, bone-implantable delivery systems have been considered as a promising strategy. This study aims to improve drug loading capacity of bone-implantable delivery systems by introducing hollow structure mesoporous bioactive glass nanospheres (HMBGs) through a sol–gel process. Particularly, such core–shell bimodal-porous structured nanoparticles were prepared through a sacrificing template using cetyltrimethylammonium bromide (CTAB) as surfactant. It was found that varying the amount of CTAB during the synthesis process is a simple and effective approach for tuning the particle size, morphology, and structure of HMBGs. For in vitro drug release, HMBGs could sustain storage and release of vancomycin hydrochloride (VAN) via diffusion-controlled mechanism, thereby inhibiting the bacteria growth in the subsequent bacterial study. Moreover, HMBGs incorporated with VAN provided a biomimetic microenvironment favored by cell adhesion and proliferation. These findings support the compatibility of HMBG nanoparticles with antibiotics and their potential application in the treatment of infectious bone defects. 相似文献
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Zhongbo Guan Yayan Wang Xiuxin Yu Yuanhui Shen Dongrong He Zhongli Tang Wenbin Li Donghui Zhang 《International Journal of Hydrogen Energy》2021,46(1):683-696
A dual-reflux pressure swing adsorption (DR-PSA) process was proposed and simulated to initially separate the blue coal gas, aiming to capture carbon dioxide (CO2) and enrich hydrogen (H2), simultaneously. With a feed flow rate of 7.290 slpm, a light product reflux flow rate of 0.505 slpm and the heavy product reflux flow rate of 3.68 slpm, the developed DR-PSA process could capture CO2 up to 64.01% with a recovery of 99.60% and enrich H2 up to 34.66% with a recovery of 97.63% from the blue coal gas (36.2% N2/28.5% H2/13.9% CO/12.7% CO2/8.7% CH4). In addition, in order to optimize the process, the effects of various operating parameters on the DR-PSA process performance in terms of product purity and recovery were discussed in detail, including the feed position, the light product reflux ratio and the heavy product reflux ratio. Moreover, the dynamic distribution behaviors of pressure, temperature and gas-solid concentration were presented to explain and evaluate the process separation performance in depth under different operating conditions. 相似文献
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Making of a layered composite using two biopolymer gels with regularly aligned voids in the inner layer is described in this article. Calcium alginate constituted the inner layer, within which voids of 500 μm diameter were embedded in monolayer or in multiple layers using a fluidic device for bubbling. The chitosan without any additional crosslinker was used to form the outer layer. The layered structure enabled compartmentalization of drug hold-up, and differential release rates. These aspects were reviewed using bovine serum albumin and vitamin B12 as model solutes. The presence of voids at the inner layer of alginate increased the uptake, raising the level of absorptivity to more than 4000%. The composite film could hold two solutes at a time. The one, held inside the alginate layer started releasing only after 1 h of dipping in the release media. The adhesive strength between layers and the response of the composite film to compressive deformation are studied here. The effect of single or multiple layers of voids in the inner layer is reviewed. The slowing of degradation rate due to chitosan-encapsulation is experimentally determined. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47599. 相似文献
19.
Novel molecularly imprinted polymer nanofibers (MIP‐NFs) were prepared for the adsorption of bisphenol A (BPA) in a water sample using the sol–gel process and the electrospinning technique. The effects of a number of synthesis parameters on the adsorption efficiency were investigated. The successful removal of BPA from MIP‐NFs was studied using UV–visible spectroscopy. The prepared MIP‐NFs were characterized by Fourier transform infrared, field emission SEM, TEM and energy dispersive X‐ray analysis. The results showed that the required molar ratio of 3‐aminopropyltriethoxysilane (APTES) to BPA was 15:1, which indicates a good performance in the rebinding test. Likewise, the molar ratio of APTES:acid:water was 1:2:9. The nylon 6 polymer solution, with a concentration of 12 wt%, showed a maximum adsorption capacity for BPA due to a decrease in the nanofiber diameter and an increase in the accessible sites. Furthermore, the maximum adsorption capacity of BPA was achieved at pH 7. Concerning the binding of BPA on MIP‐NFs, the experimental data matched well with the pseudo‐second‐order kinetics data and the Sips isotherm model. The saturated binding capacity for MIP‐NFs was predicted to be 115.1 mg g?1, which was more than twice as high as that for non‐imprinted polymer nanofibers (46.82 mg g?1). The results obtained in this study confirmed that the prepared MIP‐NFs showed considerable binding specificity for BPA in comparison with similar structural compounds such as phenol, naphthol and Naphthol AS, in aqueous solution. The binding capacity of MIP‐NFs remained almost constant after five cycles of reuse. The real sample analysis indicated that MIP‐NFs could be utilized as a useful sorbent material for the extraction of BPA from a water sample. 相似文献
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