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91.
92.
回顾了锦纶发展简史,综述了国内锦纶生产现状,并论述了我国锦纶生产发展方向,必须大力发展原料工业;加快老企业的设备改造;使其达到规模经济,大力发展差别化、高附加值、功能性纤维。同时,提出了锦纶各品种的发展趋向。 相似文献
93.
94.
煤岩配煤技术的发展与现状 总被引:3,自引:0,他引:3
煤岩学在炼焦配煤技术上的应用,使炼焦配煤手段更有效,使焦炭质量预测在生产上应用成为可能,为定性的经验配煤技术跃变到定量的科学配煤技术创造了条件。夏皮洛煤岩配煤技术是目前较好的配煤方法,其相关系数可达0.93;国内许多学者在煤岩配煤方面也做了大量研究工作,有些相关系数达0.98。目前虽然各种方法存在一定局限性,但随着计算机和图像处理技术的发展,煤岩学在指导配煤技术方面将有新的突破。 相似文献
95.
96.
Chang Yang Chengyin Liu Ning Wu Xiang Wu Yidong Li Zhiying Wang 《Neural computing & applications》2014,25(7-8):1741-1754
Collaboration representation-based classification (CRC) was proposed as an alternative approach to the sparse representation method with similar efficiency. The CRC is essentially a competition scheme for the training samples to compete with each other in representing the test sample, and the training class with the minimum representation residual from the test sample wins the competition in the classification. However, the representation error is usually calculated based on the Euclidean distance between a test sample and the weighted sum of all the same-class samples. This paper exploits alternative methods of calculating the representation error in the CRC methods to reduce the representation residual in a more optimal way, so that the sample classes compete with each other in a closer range to represent the test sample. A large number of face recognition experiments on three face image databases show that the CRC methods with optimized presentation residual achieve better performance than the original CRC, and the maximum improvement in classification accuracy is up to 12 %. 相似文献
97.
茜素红(ARS)是葸醌类化合物中茜草素型的一种,被广泛应用于电化学、光谱学等领域的研究。在酸性溶液中,茜素红主要在260 nm和422 nm处出现明显的吸收峰,而在碱性溶液中吸收峰移动到272 nm和556 nm。为了分析不同溶液环境对茜素红吸收峰波长的影响,本研究在杂化密度泛函方法B3LYP/6-311+(d)水平上优化了ARS分子在酸、碱性情况时的稳定基态构型,并采用含时密度泛函(time-dependent density functional theory,TD-DFT)方法模拟了ARS分子的电子吸收光谱。计算结果与实验得到的紫外可见吸收光谱相吻合,说明密度泛函理论用来研究茜素红的紫外可见光谱是有效可靠的。通过计算还确定了每个吸收峰对应的各个电子跃迁的贡献率以及Mulliken电荷分布。该理论与实验的结合研究为茜草素型化合物的进一步应用、分子设计、药物构效关系和化学反应规律的研究提供了重要的参考依据。 相似文献
98.
Possible use of methylbenzenes as electrolyte additives for improving the overcharge tolerances of Li-ion batteries 总被引:1,自引:0,他引:1
Based on the voltammetric behaviour of a series of methyl-substituted benzenes in 1M LiPF6/EC-DMC electrolyte, xylene was selected and tested as an electrolyte additive for overcharge protection of Li-ion batteries. From the overcharge curves, CV behaviour and SEM observations of the cells in the presence of xylene, it was found that the additive can polymerize at the overcharged voltage to form a dense layer of isolating polymer film at the cathode surface, which blocks off further oxidation of the electroactive material and electrolyte and, therefore, improves the overcharge tolerance of the Li-ion battery. In addition, the xylene additive has shown only a slight influence on the cycling behaviour. 相似文献
99.
本文从酸度系数着手,证实了K2O-CaO-Al4O久-SiO2系统中存在自释釉组成,限定了其组成范围,0.67%<K2O<1.28%,10.64%<CaO<13.62%,11.53%<Al4O3<15.32%,72.73%<SiO2<74.04%,并讨论了自释釉瓷的性能。 相似文献
100.
In this research, the kinetics for synthesizing 4-acetylphenyl benzoate (R*COOR) from benzoylation of sodium 4-acetylphenoxide via third-liquid phase-transfer catalysis was investigated. The reaction rate was observed to be strongly dependent on agitation speeds in the third-phase catalytic reaction. By forming the third-liquid phase, the observed reaction can be greatly enhanced to give a product yield of 100% in a duration of 3 min at 20 °C and 200 rpm. If a third-liquid phase was not formed in the liquid–liquid system, the reaction rate is very slow and the product yield is only 2% in 3 min at 20 °C. The reaction conducted in third-liquid phase-transfer catalytic system is faster than that in LLPTC system by 25–28 times. The amount of catalytic intermediate (QOR) in the third-liquid phase was about 50% of the catalyst initially added and kept about 30% of it remained after 1 min, and only small amounts of a catalytic intermediate residing in the organic phase were observed during the reaction using methyl t-butyl ether as the solvent. The concentration of catalytic intermediate slightly decreased with increasing reaction time, while the molar ratio of QOR to benzyl tri-n-butylammonium cation in the third-liquid phase remained almost constant after 1 min and increased with increasing agitation speeds. The experimental results were well described by the pseudo-first-order kinetics. The present work shows an effective method to synthesize 4-acetylphenyl benzoate. 相似文献