H_2辉光放电清洗时轰击器壁的离子能量测量与分析

一、引言 辉光放电是清洗锻炼环流器真空室器壁的有效手段。H_2辉光放电时,氢离子轰击器壁与器壁中的C和O发生化学反应,生成CH_4,H_2O等气体;同时,这些离子提供能量使得吸附在器壁表面的杂质气体脱附,从而被泵出真空室外,达到清洗锻炼的目的。由于辉光放电时,离子轰击的能量较高,会引起一定的溅射沉积。我们在模拟真空室(六通装置)进行了辉光放电,对各种参数下的离子能量进行了测量,从中找出了离子能量与极间电压(阳极与器壁之间的电压)、放电电流、以及气压、离子流密度之间的某些关系。     

预试环中H_2及掺杂甲烷的辉光放电清洗

本文给出了在预试环中产生和维持辉光放电的基本参数、氢气(H_2)及氢气掺杂甲烷(H_2/CH_4)辉光放电清洗过程中的质谱分析结果以及氢气辉光放电清洗处理后的样品表面SIMS(二次离子质谱)结果,并进行了讨论。     

桶式离子源参数计算与实验的比较

在用H_2、D_2和He气体运行的情况下,把桶式离子源的引出电流、放电电流和灯丝电流的计算与TEXTOR装置上的实验结果做了比较。     

大气压射流等离子体放电特性及其灭菌效果

 介绍了一种同轴电极的射流等离子体发生装置,可以直接在大气中将生成的氦气辉光放电射流等离子体喷出进行杀菌消毒,无需反应容器和真空系统,并从电压、频率、流速等方面讨论了该同轴等离子体发生器的放电特性。在稳定的放电条件下,利用实验装置进行了大气压下的等离子体灭菌实验,验证了本装置在等离子体灭菌应用上的可行性和易操作性。灭菌结果表明：在最初的2 min内,细菌减小趋势明显,3 min后细菌几乎全部消亡。     

HL-2M 装置初始等离子体放电阶段的直流辉光放电清洗系统研制

基于 HL-2M 托卡马克初始等离子体放电的工程需求,设计并研制了直流辉光放电清洗系统,包括电 极、馈线、电源、控制以及监测等关键部件和辅助子系统。研制完成后开展了系统装配和工程调试,并投入到首 次等离子体放电。实验结果表明,该直流辉光放电系统运行稳定、可靠,且此辉光放电清洗显著降低了真空室本 底杂质浓度,能满足 HL-2M 装置初始等离子体放电的壁条件需求。     

HL-2A托卡马克装置真空系统

介绍了HL 2A装置真空系统研制。它由真空主抽气系统、抽气偏滤器、直流辉光放电清洗系统组成。主抽气系统提供了装置真空室从大气到高真空、烘烤除气、直流辉光放电清洗所需要的抽气能力。抽气偏滤器初步实现了托卡马克放电过程中边缘粒子的抽运与控制;直流辉光放电清洗系统保证了装置良好的真空器壁条件。介绍了这些系统的初步运行情况,并给出了其测试结果。HL 2A装置首轮物理实验运行时真空室极限真空度达到4.6×10-6Pa,12h总漏放气率为1.8×10-5Pa·m3·s-1。     

HL-2A装置真空系统

现代核聚变实验装置要求的真空系统必须实现以下主要功能：（1）装置真空室的零部件及总体抽空和检漏；（2）真空室的烘烤除气（H2O）；（3）辉光放电清洗和面对等离子体部件的锻炼及原位处理；（4）边缘粒子的抽运与控制；（5）等离子体放电实验运行。     

N2交流辉光放电等离子体喷束的光谱测量及特性研究

建立了一套交流放电产生N2等离子体喷束的装置,该装置可对氮气进行高达15 kV连续放电.采用浓度调制光谱技术对放电辉光光谱进行探测,并对实验中放电电流和光谱信号的关系进行了讨论.沿着束流的轴向探测了不同位置N2等离子体的发射光谱,发现其激发态振动温度随着束流的下降先降低继而升高,并根据实验条件分析了其变化规律和产生机理.研究了束流中N2 /N2比例变化过程,发现随着束流向下两者比例逐渐升高,并结合实验装置进行讨论.     

间隙绝缘电极辉光放电实验观察

实验研究了ITER H2/He辉光放电壁处理(GDC)系统的电极合理的间隙绝缘参数及标定辉光过程中沉积在电极头部的热负载.进行了H2/He击穿电压特性试验,在ITER GDC预期的壁离子电流密度条件下研究了H2/He辉光放电电压和试验电极上热负荷与压强的关系、试验电极启辉耐受特性、试验电极温度与热负荷的关系以及在不同区...     

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用火花预电离辅助介质阻挡放电装置在大气压空气中实现了均匀的类辉光放电。通过用光谱模拟法和波尔兹曼图解法对N 2 第一负带系B2Σ→X 2Σ(0,0)带发射谱线的分析,对放电过程中N 2 的转动温度进行了诊断。研究了不同频率和放电模式下转动温度的变化规律,对由两种方法计算所得的温度进行了对比。实验结果表明,转动温度会随着外加频率的增加而缓慢的增加;当放电从类辉光模式变到丝状放电模式时,转动温度会有70K左右的升高。     

Variation of microstructure with carbonation in lime and blended pastes

Carbonation, as a reaction of the curing process of both, cement and lime binders, modifies the microstructure. Several microstructure properties, namely porosity, pore size distribution, surface fractal dimension, and specific surface area have been investigated in this study to describe the effect of carbonation on microstructure. Both carbonated and non-carbonated pastes of lime and blended pastes of lime and cement having varying water/binder (W/B) ratios are studied. Results show that carbonation decreases the porosity, but not with the same intensity in all pore size ranges. The highest modification is between 0.03 μm and 0.01 μm in lime pastes and between 0.2 μm and 0.02 μm in 50% lime pastes, while in 80% lime pastes the modification is very small. It is also observed that carbonation is a function of the binder composition but not of the W/B ratio. Moreover, surface fractal dimension decreases during the carbonation process, while the specific surface area varies depending of the binder composition.     

CaO高温分离CO2过程的数值模拟

钙基吸收剂煅烧-碳酸化循环法(CCRs)是一种新兴的分离燃煤锅炉尾部烟气中CO2的方法.CaO与CO2碳酸化反应对于CCRs法的应用起着非常重要的作用.本文采用随机孔隙模型(RPM)对CaO与CO2碳酸化反应过程进行了研究,结果表明,适当提高CaO与CO2碳酸化反应的温度和系统压力,增加CaO吸收剂的初始孔隙率、优化CaO的初始比表面积等措施能够有效提高CaO碳酸化转化率和对CO2的吸收容量.     

Vibrational spectra of α-molybdic acid-MoO3.H2O

Their and Raman spectra of molybdenum trioxide—monohydrate are studied assuming an effective tetrahedral Mo-O coordination and isolated water molecules, although the crystallographic coordination is six-fold with two long Mo-O distances. Based onCt symmetry, the group theoretical analysis has been carried out and a vibrational assignment is proposed. The nature of hydrogen bonding and the librational modes of water molecules are discussed. The factor group splitting forv3, the asymmetric stretching mode of MoO₄ ⁼ ion, is large indicating strong interchain coupling.     

Hydration and carbonation of monoclinic C2S and C3S studied by Raman spectroscopy

We present a micro‐Raman study on the hydration and carbonation of the main silicate phases of Portland cement, i.e. monoclinic dicalcium silicate (C₂S) and monoclinic tricalcium silicate (C₃S). We investigate the reaction products and the loss of crystallinity induced by hydration on these two compounds. In the CO₂‐contaminated pastes we find that calcite, aragonite, and vaterite are inhomogeneously formed. We study sample cross sections to evaluate the maximum depth at which CaCO₃ is formed. We find that carbonation is limited to the first 500–1000 µm from the surface in the C₃S pastes, while in C₂S pastes CaCO₃ is formed well beyond this depth. Our results show the great potential of Raman spectroscopy in the study of the chemistry of cements. Copyright © 2006 John Wiley & Sons, Ltd.     

X光光电子能谱法测定胶片中氟,硅和铝的研究

应用Ｘ光光电子能谱法测定了几种彩色胶片表面层中氟的１ｓ能级的结合能；分别比较了水处理前后、溅蚀前后胶片护膜层氟的变化，表明氟化物分布在护膜最表层，是一种易溶于水的氟化物；测定了彩色片护膜层所含硅２ｐ能级的结合能，与自制彩色片护膜层测定结果比较，优质片含一种较多负电性，用与自制片的无机硅不同的硅化物作毛面剂；对溅蚀前后优质片和自产彩色片中的硅铝比变化进行比较，提出优质彩色片Ｆ－４００的护膜层可能是双     

Formation and Evolution of Carbonate Species in Na-Doped Al2O3 and V2O5-Al2O3

A study is carried out by FT-IR spectroscopy of the carbonate species formed upon interaction of CO₂ with alumina and vanadia-alumina catalysts doped with sodium. It is found that the presence of sodium enhances the ability of the catalyst surface to adsorb CO₂, yielding to carbonate formation. The species formed changes in the presence of vanadium, shifting the ν_COO stretching bands towards higher wavenumbers than those recorded in Na-Al₂O₃ systems.     

Structure of the rutile TiO2(011) surface in an aqueous environment

First principles simulations are carried out to investigate the structure and stability of the rutile TiO2(011) surface in contact with liquid water. Whereas this surface exhibits a (2×1) reconstruction in vacuo, our results show that the interaction with water leads to an inversion of the stabilities of the reconstructed and unreconstructed surfaces. This indicates that surface structures determined in vacuo or at low water coverages are not generally representative of those occurring in the aqueous environments typical of most photocatalytic applications of TiO2.     

Dynamical and structural properties of adsorbed water molecules at the TiO2 rutile-(110) surface: interfacial hydrogen bonding probed by ab-initio molecular dynamics

ABSTRACT

Ab-initio molecular dynamics (AIMD) simulations have been carried out to study a range of different and energetically-accessible adsorbed-water configurations and motifs for their vibrational and structural characteristics, in contact with rutile-(110) interfaces at 100?K. The radial pair distribution function between the titanium atoms at the interface and the hydrogen and oxygen atoms in the water monolayer show an orientation of the water molecules parallel to the surface of titania, and with hydrogen atoms pointed in the opposite direction to the surface. In some cases, a distinctive vibrational frequency region between 2500 and 3000?cm^?1 has also been observed, due to a strong dispersion interaction between water molecules. This behaviour is also seen in experimental studies of thin-film water coverage on TiO₂ surfaces.     

管道中CaO颗粒吸收CO2的格子Boltzmann方法模拟

采用格子Boltzmann方法对多孔CaO颗粒与CO₂之间的气固反应过程进行模拟.主要研究在二维矩形截面管道中雷诺数(Re)和孔隙率对单个CaO颗粒吸收CO₂效率的影响.结果表明:增大Re会相应提高CaO颗粒吸收CO₂气体的效率.同时对于同一Re,CaO颗粒吸收CO₂气体的效率随其孔隙率呈非线性变化,这是由于不同孔隙率颗粒固体量和渗透率存在差别因而影响化学反应的速率.     

Infrared Spectra Interpretations of Clay-Adsorbed Water in Relation to the “Anomalous” Water Controversy

Abstract

The nature of surface adsorbed water has been the subject of countless investigations. Much of the discussion has centered around the degree and strength of H-bonding to surface groups and between adjacent water molecules.^1,2 Water condensed into glass or quartz capillaries sometimes has unusual properties. This unusual water has been referred to as “orthowater,”³ “anomalous water,”^4,5,6 and “polywater”^7,8 and was thought by some to be polymers of water formed by specific surface catalysis.^1–3 Several possible structures of “polywater” have been suggested which require formation of symmetrical or very strong H-bonds between water molecules.^4,6,7 Infrared spectra of polywater have been presented^7,8 and the strongest absorption band which appeared at 1595 cm^?1 was assigned to the symmetric O-H-O bond. However, more recent investigations suggest that the observed polywater bands may actually be SO₄ ^2-, -COOH^?, or HCO₃ ^? bands, impurities collected by surface diffusion,⁹ or bands of a HNO₃ solution formed by corona discharge.¹⁰ Other observers^11,12 suggest that polywater may be a hydrosol formed by surface contaminates.