使用地热能的吸收式制冷系统

吸收式制冷系统可以利用低品位的热源来制冷，相对于常见的蒸汽压缩式制冷系统而言在这方面具有优势。我国是一个地热资源很丰富的国家，为了充分利用这一资源，我们有必要对以地热为热源的吸收式制冷系统进行研究。本文着重分析了使用地热资源的溴化锂吸收式制冷系统。     

Effect of calcination temperature on the characteristics of SO<Emphasis Type="Italic">sk</Emphasis>4/2-/TiO<Subscript>2</Subscript> catalysts for the reduction of NO by NH<Subscript>3</Subscript>

The catalytic activity of sulfated titania (ST) calcined at a variety of temperatures has been investigated for selective catalytic reduction (SCR) of NO by NH₃. The NO removal activity of ST catalyst mainly depends on its sulfur content, indicating critical role of sulfur species on the surface of TiO₂. The role of sulfur is mainly the formation of acid sites on the catalyst surface. The presence of both BrØnsted and Lewis acid sites on the surface of sulfated titania has been identified by IR study with the adsorption of NH₃ and pyridine on ST. The reduction of the intensity of IR bands representing BrØsted acid sites is more pronounced than that revealing Lewis acid sites as the calcination temperature increases. It has been further clarified by IR study of ST500 catalyst evacuated at a variety of temperatures. The NO removal activity also decreases with the increase of the catalyst calcination temperature. It simply reveals that BrØnsted acid sites induced by sulfate on the catalyst surface are primarily responsible for the enhancement of catalytic activity of ST catalyst containing sulfur for NO reduction by NH₃.     

Chlorophyll adsorption on acid-activated clay

An acid-activated clay (Çanakkale montmorillonite from Turkey) was used to adsorb chlorophyll from hexane solutions. The phenomenon seems to be mainly driven by the interaction of chlorophyll with acid sites. The adsorption of chlorophyll on Brönsted acid sites was indicated by a characteristic infrared band for the -OH group at 3671 cm^?1. The variations in the structure of clay mineral and chlorophyll during adsorption have been examined by differential thermal analysis, thermogravimetry and infrared spectroscopy of the activated clay before and after adsorption of chlorophyll. Oxidation of adsorbed chlorophyll was completed at quite a high temperature.     

Vapor Phase Growth of Centimeter-Sized Band Gap Engineered Cesium Lead Halide Perovskite Single-Crystal Thin Films with Color-tunable Stimulated Emission

Single crystal metal halide perovskites thin films are considered to be a promising optical, optoelectronic materials with extraordinary performance due to their low defect densities. However, it is still difficult to achieve large-scale perovskite single-crystal thin films (SCTFs) with tunable bandgap by vapor-phase deposition method. Herein, the synthesis of CsPbCl_3(1–x)Br_3x SCTFs with centimeter size (1 cm × 1 cm) via vapor-phase deposition is reported. The Br composition of CsPbCl_3(1–x)Br_3x SCTFs can be gradually tuned from x = 0 to x = 1, leading the corresponding bandgap to change from 2.29 to 2.91 eV. Additionally, an low-threshold (≈23.9 µJ cm⁻²) amplified spontaneous emission is achieved based on CsPbCl_3(1–x)Br_3x SCTFs at room temperature, and the wavelength is tuned from 432 to 547 nm by varying the Cl/Br ratio. Importantly, the high-quality CsPbCl_3(1–x)Br_3x SCTFs are ideal optical gain medium with high gain up to 1369.8 ± 101.2 cm⁻¹. This study not only provides a versatile method to fabricate high quality CsPbCl_3(1–x)Br_3x SCTFs with different Cl/Br ratio, but also paves the way for further research of color-tunable perovskite lasing.     

政策法制与能源产业推动之探讨——以德国再生能源法为中心

全球传统石化能源耗竭及气候变迁等负面效应日益严重,以永续发展为目标,再生能源之开发利用备受关注,已成为世界各国能源政策的主要施政方针,其中多以立法手段积极推动.综观各国已提出亦或正在施行的政策和措施,皆由订定法令来体现,以法律的形式确立发展目标,再透过具体而明确的强制规范或经济激励措施,进而得其实质成效.德国再生能源法相关法规范即为明证.德国于2000年制定全球首部再生能源优先法(Gesetz fürden Vorrang Erneuerbarer Energien),简称再生能源法(Ernererbare-Energien-Gesetz,EEG),至今已历多次修法.本文将从德国再生能源法制探讨,观其核心固定电价制度(Feed-in Tariff,FIT)与近年修法方向,说明德国再生能源产业发展之背景及现况,希祈能就推动发展再生能源有所帮助.     

Rochow-Müller反应制备甲基氯硅烷单体工艺的研究进展

Rochow-Müller反应是一种直接合成甲基氯硅烷的方法。由于其原料易得,产物收率高,工艺较易实现,成为有机硅工业单体生产的主流工艺。到目前为止,铜基催化剂仍为Rochow-Müller反应的核心催化剂,催化性能的改善对该工艺的提升具有重大意义。在探索高效催化剂和理解其机理方面已取得相关进展,但由于副产物多,复杂性高,对该反应真实反应路径的追踪仍然较为困难。对Rochow-Müller反应的热力学过程、铜基催化剂及助催化剂的应用、反应机制及动力学过程和工艺条件的影响进行综述讨论。希望这项工作能够准确地反应Rochow-Müller反应催化工艺的最新进展,并可以促进有机硅工业的可持续性发展。     

Alkane cracking reactions in zeolites with coadsorbed metal halides

HY which is loaded with SbF₅, BCl₃, or BF₃ at low coverages, one metal halide molecule per Brønsted acid site, is shown to be active in the isomerization and cracking of n-hexane and n-butane at room temperature. In contrast, NaY with the same metal halide loading shows greatly reduced activity under identical reaction conditions. The cracking reaction was repeated with DY in place of HY, demonstrating deuterium incorporation into the hexane isomer and light alkane products through interaction with the Brønsted site. Flow reactor studies demonstrate that the conversion is not constant as a function of time on stream, going through an induction period, reaching a maximum, at around 400 s, and then decaying to ~1% after 1 h.     

基于普吕克直线的多线结构光视觉传感器标定方法

针对多线结构光系统的快速标定,提出了一种基于普吕克直线的标定方法。传统的线结构光标定方法大多以单点的形式进行提取和坐标系转换,从而获得平面方程。然而单点数量较多会导致操作复杂,不适用于多线结构光的标定。为了解决这个问题,提出了一种新的标定方法,该方法在标定过程中全部采用普吕克矩阵的形式,而不是直接使用点特征。该方法有利于在摄像机坐标系下快速准确地获得光平面方程。同时设计了一种与该方法相对应的用于标定多线结构光的平面标定靶标。为了将一般直线转换为普吕克直线,将图像平面维度延展,定义了一个新的图像空间。为了对普吕克直线的坐标系进行转换,重新表达了基于普吕克直线的透视投影模型。基于普吕克空间中直线与平面的性质,对多条结构光线的普吕克矩阵进行合并即可高效地构造出线性的矩阵方程,从而进一步拟合出结构光平面方程。实验验证了所提方法并证明了校准精度的显著提高,当测试距离为1.8 m时,测量得到的三维点的RMS误差在0.08 mm之内。     

β-环糊精协同乙烯基咪唑离子液体脱除溶剂油中的萘

采用1-乙烯基-3-正丁基溴代咪唑离子液体（[VBIM]Br）为脱除剂,在β-环糊精协同作用下萃取溶剂油中的萘。本实验考察了不同单因素条件在[VBIM]Br离子液体与β-环糊精共同作用下对溶剂油中脱萘率的影响,同时通过响应面法优化脱除工艺条件。实验结果表明：[VBIM]Br离子液体与β-环糊精共同作用下对萘的萃取率比单独利用[VBIM]Br离子液体提高了15%以上,萃取率达到90%以上。离子液体简单回收后,重复使用5次过后,脱除率仍在80%以上。实验通过红外分析和紫外光谱分析了[VBIM]Br离子液体协同β-环糊精脱萘的机理,与[VBIM]Br离子液体协同作用下,β-环糊精对萘存在包合作用,实现了对溶剂油中萘的脱除。     

The Effect of Different Active Sites on the Catalytic Activity of Fe-ZSM-5 Zeolite for N2O Direct Decomposition

Fe-modified ZSM-5 zeolites (Si/Al = 25) were prepared by adopting the liquid ion-exchange method with nitrate and oxalate of iron as Fe precursors and their catalytic performance was studied in the N₂O decomposition reaction. The results of FT-IR and H₂-TPR investigations indicated that (i) part of the iron ions could replace Brönsted acid protons at the straight channel wall (α sites), intersection of straight and sinusoidal channels (β sites), and sinusoidal channel wall (γ sites) within the ZSM-5 zeolite; and (ii) different Fe precursors gave rise to various distributions of α, β, and γ sites. We observed that the Fe-ZSM-5 catalyst prepared with iron oxalate as Fe precursor outperformed the ones prepared with iron nitrate as Fe precursor in the direct decomposition of N₂O. Furthermore, the catalytic activity of iron ions located at the α sites was higher than those of iron ions located at the β and γ sites.