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1.
本文采用高压均质结合对辊挤压工艺对天然凹凸棒石进行棒晶解离得到了纯度较高和比表面积较大(133.7 m2/g)的纳米解离凹凸棒石. 进一步通过机械共混法分别将天然凹凸棒石和纳米解离凹凸棒石与硅橡胶生胶复合制备了天然凹凸棒石-硅橡胶和纳米解离凹凸棒石-硅橡胶材料,研究了天然凹凸棒石和纳米解离凹凸棒石对凹凸棒石/硅橡胶复合材料热氧化降解和老化性能的影响. 结果表明,天然凹凸棒石-硅橡胶和纳米解离凹凸棒石-硅橡胶在300 oC热氧老化处理0.5 h后,相比于纯硅橡胶,初始5%失重温度从385 oC提高至396∽399 oC. 系列表征结果表明,天然凹凸棒石和纳米解离凹凸棒石增强了纳米粒子与硅橡胶之间的相互作用从而抑制了纳米颗粒聚集,并且可显著提高硅橡胶侧链Si-CH3的保存率,从而提高了该复合材料的热氧化降解和老化性能. 此外,纳米解离凹凸棒石可大大抑制纳米粒子的长大;因此老化后,纳米解离凹凸棒石-硅橡胶表现出了比硅橡胶(10.6%、7.4%和5.0%)更高的拉伸强度、断裂伸长率和撕裂强度保留率(40.6%、34.9% 和30.1%). 相似文献
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The aim of this work was to evaluate the influence of US on the properties of the fluconazole emulsions prepared using imidazolium-based ILs ([Cn C1im]Br). The effects of the preparation method (mechanical stirring or US), US amplitude, alkyl chain length (of [C12C1im]Br or [C16C1im]Br), and IL concentration on the physicochemical properties were evaluated. Properties such as droplet size, span index, morphology, viscosity encapsulation efficiency, and drug release profile were determined. The results showed that US-prepared emulsions had a smaller droplet size and smaller polydispersity (Span) than those prepared by mechanical stirring. Additionally, the results showed that emulsions prepared with [C16C1im]Br and US had spherical shapes and increased stability compared to emulsions prepared by MS, and also depended on the IL concentration. The emulsion prepared by US at 40% amplitude had increased encapsulation efficiency. US provided a decrease in the viscosity of emulsions containing [C12C1im]Br; however, in general, all emulsions had viscosity close to that of water. Emulsions containing [C16C1im]Br had the lowest viscosities of all the emulsions. The emulsions containing the IL [C16C1im]Br had more controlled release and a lower cumulative percentage of drug release. The IL concentration required to prepare these emulsions was lower than the amount of conventional surfactant required, which highlights the potential synergic effects of ILs and US in preparing emulsions of hydrophobic drugs. 相似文献
3.
In the past decade, big data has become increasingly prevalent in a large number of applications. As a result, datasets suffering from noise and redundancy issues have necessitated the use of feature selection across multiple domains. However, a common concern in feature selection is that different approaches can give very different results when applied to similar datasets. Aggregating the results of different selection methods helps to resolve this concern and control the diversity of selected feature subsets. In this work, we implemented a general framework for the ensemble of multiple feature selection methods. Based on diversified datasets generated from the original set of observations, we aggregated the importance scores generated by multiple feature selection techniques using two methods: the Within Aggregation Method (WAM), which refers to aggregating importance scores within a single feature selection; and the Between Aggregation Method (BAM), which refers to aggregating importance scores between multiple feature selection methods. We applied the proposed framework on 13 real datasets with diverse performances and characteristics. The experimental evaluation showed that WAM provides an effective tool for determining the best feature selection method for a given dataset. WAM has also shown greater stability than BAM in terms of identifying important features. The computational demands of the two methods appeared to be comparable. The results of this work suggest that by applying both WAM and BAM, practitioners can gain a deeper understanding of the feature selection process. 相似文献
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GAO Jian-kui LI Yi-jie ZHANG Qin-nan LIU Bing-wei LIU Jing-bo LING Dong-xiong LI Run-hua WEI Dong-shan 《光谱学与光谱分析》2021,41(11):3347-3351
聚醚醚酮(PEEK)由于其耐热、耐腐蚀、耐辐照、抗疲劳、电绝缘性等优良性能,在许多领域可以代替金属、陶瓷等传统材料而得到广泛应用。特别是随着5G技术的发展和应用,PEEK已经成为5G热门材料。在PEEK材料实际应用中,温度的影响是一个非常重要和关键的因素。主要研究了PEEK太赫兹光谱以及温度对PEEK太赫兹光谱特性的影响。通过利用太赫兹透射光谱技术,同时结合控温装置,在温度从25~300 ℃均匀上升过程中,每间隔5 ℃测试得到PEEK片状样品的太赫兹时域光谱数据,利用光学参数提取算法可以得到PEEK的吸收系数、介电常数等光学参数,进一步得到特定频率下光学常数随温度的变化趋势,从而对材料进行表征和分析。在0.5~4 THz有效光谱范围内,实验结果表明,在常温(25 ℃)下,PEEK在3.5 THz具有一个明显的特征吸收峰。在25~300 ℃这个温度范围内,在1 THz频率下,PEEK的吸收系数、介电常数相对于室温分别有4.38%和5.0%的波动,同时PEEK在常温下在1 THz的介电损耗正切值为2.5×10-3,相比于PMMA和PE等高分子材料,PEEK的介电损耗正切值要低得多,且在升温过程保持相对稳定,表明PEEK在太赫兹频段的光谱特性具有很好的热稳定性和较低的介电损耗。研究结果表明,太赫兹光谱技术可以结合温控装置,通过材料的光学参数对高分子材料热稳定性进行研究和表征,同时还可以得到材料在不同温度下的介电性质。太赫兹光谱技术具有快速、高效、无标记、无损伤等优势,只需要压片就可以对固体样品进行测试,对于研究材料内部缺陷、稳定性以及材料的鉴别等具有很好的研究意义。同时本实验的测试数据可以为PEEK材料在不同温度下5G和6G等高频通信应用提供参考。 相似文献
6.
Divya Kumar Vemuri Rambabu Gundla Naresh Konduru Ravindra Mallavarapu Naresh Kumar Katari 《Biomedical chromatography : BMC》2022,36(6):e5363
Favipiravir finished dosage was approved for emergency use in many countries to treat SARS-CoV-2 patients. A specific, accurate, linear, robust, simple, and stability-indicating HPLC method was developed and validated for the determination of degradation impurities present in favipiravir film-coated tablets. The separation of all impurities was achieved from the stationary phase (Inert sustain AQ-C18, 250 × 4.6 mm, 5-μm particle) and mobile phase. Mobile phase A contained KH2PO4 buffer (pH 2.5 ± 0.05) and acetonitrile in the ratio of 98:2 (v/v), and mobile phase B contained water and acetonitrile in the ratio of 50:50 (v/v). The chromatographic conditions were optimized as follows: flow rate, 0.7 mL/min; UV detection, 210 nm; injection volume, 20 μL; and column temperature, 33°C. The proposed method was validated per the current International Conference on Harmonization Q2 (R1) guidelines. The recovery study and linearity ranges were established from the limit of quantification to 150% optimal concentrations. The method validation results were found to be between 98.6 and 106.2% for recovery and r2 = 0.9995–0.9999 for linearity of all identified impurities. The method precision results were achieved below 5% of relative standard deviation. Forced degradation studies were performed in chemical and physical stress conditions. The compound was sensitive to chemical stress conditions. During the study, the analyte degraded and converted to unknown degradation impurities, and its molecular mass was found using the LC–MS technique and established degradation pathways supported by reaction of mechanism. The developed method was found to be suitable for routine analysis of research and development and quality control. 相似文献
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主动冷却点阵夹层防热结构温度响应计算模型北大核心CSCD 总被引:2,自引:2,他引:0
针对点阵夹层结构主动热防护问题,建立了夹层结构面板和芯体导热与冷却剂对流耦合的非稳态传热理论模型,利用有限体积法离散控制方程并在MATLAB中进行了迭代求解.模型首次考虑了面板与夹芯杆之间的收缩热阻,并利用分离变量法得到了收缩热阻的近似解析解.基于单胞模型和周期性边界条件,模拟得到了模型所需的表面对流传热系数h_(b)和h_(fin).最后,选取多单胞计算工况进行数值模拟和理论模型对比,并讨论了收缩热阻对模型预测精度的影响.结果表明:理论模型能够准确预测夹层结构及内部流体的温度变化,理论与仿真之间的最大误差不超过1%;随着外加热流密度不断增大,忽略收缩热阻使得计算结果造成的误差不断增大;与数值模拟相比,理论模型可显著地减少计算时间并节省计算资源,尤其适用于非均匀、非稳态复杂热载荷下点阵夹层结构的温度响应计算. 相似文献
9.
采用生物质原料腰果酚和9,10-二氢-9-氧杂-10-膦杂菲-10-氧化物(DOPO)为原料, 合成了一种磷杂菲改性腰果酚多元醇(P-Cardanol-Polyol), 并利用核磁共振氢谱和磷谱对其结构进行了表征. 利用P-Cardanol-Polyol对聚氨酯硬泡(RPUF)进行阻燃改性, 得到一系列阻燃聚氨酯硬泡. 考察了P-Cardanol-Polyol的用量对阻燃聚氨酯硬泡的形貌、 密度、 热导率、 压缩性能、 热稳定性以及阻燃性能的影响. 研究结果表明, P-Cardanol-Polyol对聚氨酯硬泡的密度影响可以忽略不计; 随着P-Cardanol-Polyol的加入, 阻燃聚氨酯硬泡的平均孔径逐渐减小, 热导率也逐渐降低. 未改性聚氨酯硬泡的最大热释放速率和总放热量分别为390 kW/m2和31.9 MJ/m2, 阻燃聚氨酯硬泡则降低至340 kW/m2和24.6 MJ/m2. 此外, 阻燃聚氨酯硬泡的压缩强度比未改性聚氨酯硬泡提升了约13%. 炭层分析结果表明, P-Cardanol-Polyol能够促进聚氨酯硬泡形成连续致密且具有良好抗热氧化性能的炭层, 有利于减少燃烧过程中可燃性气体的逸出, 从而提升阻燃性能. 相似文献
10.
将有机物2,5-二溴对苯二甲酸(H2L1)和2,2′-联吡啶(L2)作为双配体,使用溶剂热法和七水合硫酸锌(ZnSO4·7H2O)、六水合硝酸钴(Co(NO3)2·6H2O)分别反应,得到配合物[Zn(L1)(L2)(H2O)]n(1)和配合物[Co(L1)(L2)(H2O)]n(2)。采用单晶X射线衍射、元素分析、红外光谱、紫外光谱、荧光光谱、热重分析等测试方法对这两种物质进行分析研究。单晶测试结果表明配合物1是单斜晶系,以Zn2+配位连接L2-1与L2形成一维链状结构,各条链在分子间氢键和π…π共轭作用下有规律地堆叠形成三维网络结构。配合物2是三斜晶系,Co1离子和Co1i离子由H2L1上的羧酸氧原子O4和O4i连接,形成双齿螯合的配位结构单元,以Co2+配位连接 L2-1和L2形成二维网格结构,各层在O—H…O分子间氢键和范德瓦耳斯力作用下有规律的堆叠形成三维网络结构。配合物1和2均含有芳香杂环、羧基杂环和氮杂环,具有良好的荧光性质和热稳定性,最大发射波长分别为345 nm和333 nm。 相似文献