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121.
Metallurgical and Materials Transactions B - Basic oxygen furnace (BOF) steel slag is a main byproduct that is produced during the converter steelmaking process. The volume instability and fast...  相似文献   
122.
Neural Processing Letters - This paper discusses the global exponential stability for a class of hybrid non-autonomous neural networks (HNNNs) with Markovian switching, which includes the factors...  相似文献   
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The high cost of noble metal catalysts has been a great bottleneck for the catalyst industry. Using the noble metal at a single-atom level for catalytic applications could dramatically decrease the cost. The impacts of single Pt atoms on the photocatalytic performance of Ag3VO4 have been investigated and reported. In this report, single Pt atoms were anchored on the surface of Ag3VO4 (AVO) as a cocatalyst, and the resultant composite photocatalyst has been studied for photocatalytic H2 production from water driven by visible light. The as-prepared AVO particles are hollow nanospheres in the monoclinic phase with a bandgap of 2.20 eV. The light absorption edge of AVO/Pt is slightly red-shifted compared to that of the pristine AVO, indicating more visible light absorption of AVO/Pt. The XPS peaks of Ag, V, and Pt exhibit a significant shift after AVO and Pt get into contact, suggesting the strong interaction between the surface Ag and V atoms, and single Pt atoms. After 3-h illumination, the photocatalytic H2 evolution amount from AVO/Pt is improved up to 1400 μmol, which is 2.8 times that on the bare AVO. Such efficient photocatalytic H2 evolution on AVO/Pt is still maintained after five reaction cycles. The better photocatalytic performance of AVO/Pt has been attributed to the more efficient visible light utilization and the lower interfacial charge transfer resistance, as demonstrated in the DRS and EIS spectra. The presence of the surface Pt atoms also leads to a higher amount of reactive radicals, which could efficiently promote the surface redox reactions.  相似文献   
125.
Guo  Fan  Ren  Lihong  Jin  Yaochu  Ding  Yongsheng 《Natural computing》2019,18(4):747-756
Natural Computing - The fiber stretching process plays the key role in the process of fiber production and its effects is measured by the stretching ratio. The stretching ratio is determined by the...  相似文献   
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张娜  秦品乐  曾建潮  李启 《计算机应用》2019,39(6):1816-1823
针对在灰度图像着色领域中,传统算法信息提取率不高、着色效果不理想的问题,提出了基于密集神经网络的灰度图像着色算法,以实现改善着色效果,让人眼更好地观察图片信息的目的。利用密集神经网络的信息提取高效性,构建并训练了一个端到端的深度学习模型,对图像中的各类信息及特征进行提取。训练网络时与原图像进行对比,以逐渐减小网络输出结果的信息、分类等各类型的损失。训练完成后,只需向网络输入一张灰度图片,即可生成一张颜色饱满、鲜明逼真的彩色图片。实验结果表明,引入密集网络后,可有效改善着色过程中的漏色、细节信息损失、对比度低等问题,所提算法着色效果较基于VGG网络及U-Net、双流网络结构、残差网络(ResNet)等性能优异的先进着色算法而言取得了显著的改进。  相似文献   
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PEM-based electrolytic air dehumidification is innovative in dehumidification that requires high precision and small space due to its high efficiency, compactness, and cleanness. However, the system dehumidification performance and durability are limited by using commercial Anatase-IrO2 catalysts. In this study, two types of structurally modified OER catalyst materials, ATO-IrO2 and ND-MnO2-IrO2, are developed to improve the performance of the system. System experiments showed that, compared to the commercial catalysts, the use of ATO-IrO2 and ND-MnO2-IrO2 as the anode catalyst can improve the dehumidification performance by 45% and 20%, respectively. Furthermore, in 50-h accelerated aging tests, the attenuation rates of the ATO-IrO2 and ND-MnO2-IrO2 systems are 3% and 8% respectively, which are far lower than the 35% attenuation of commercial catalyst. The results indicate that, as catalysts with a classic core-shell structure, ATO-IrO2 and ND-MnO2-IrO2 still have a significant impact on improving the performance of the electrolytic dehumidification systems.  相似文献   
130.
Artificial nitrogen fixation is emerging as a promising approach for synthesis of ammonia at mild conditions. Inspired by biological nitrogen fixation based on bacteria containing iron, zinc doped Fe2O3 nanoparticles are proposed as an efficient and earth abundant electrocatalyst for converting N2 to NH3. In neutral media, it achieves a maximum Faradaic efficiency (FE) of 10.4% and a large NH3 yield rate of 15.1 μg h?1 mg?1cat. at ?0.5 V vs. reversible hydrogen electrode. This catalyst also exhibits excellent selectivity and stability. Theoretical calculations suggest the reaction follows the associative enzymatic mechanism and it has a barrier of as low as 0.68 eV.  相似文献   
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