基于DBD 悬浮电极低温等离子体杀菌消毒仪研制

基于介质阻挡放电(DBD)原理,研究设计了一种悬浮电极式的低温等离子体发生设备,产生的等离子体温度较低且对人体安全,可直接接触。用所研制的低温等离子体发生设备对大肠杆菌做了灭活实验,实验结果表明,该设备产生的低温等离子体对大肠杆菌作用10s 以上,在等离子体有效作用区内大肠杆菌杀灭率为100%,表明所研制的低温等离子体发生设备具有很好的杀菌消毒效果。     

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基于介质阻挡放电(DBD)原理,研究设计了一种悬浮电极式的低温等离子体发生设备,产生的等离子体温度较低且对人体安全,可直接接触。用所研制的低温等离子体发生设备对大肠杆菌做了灭活实验,实验结果表明,该设备产生的低温等离子体对大肠杆菌作用10s 以上,在等离子体有效作用区内大肠杆菌杀灭率为100%,表明所研制的低温等离子体发生设备具有很好的杀菌消毒效果。     

水蒸气／氨活化在脉冲电晕脱硫工业中试装置上的应用

脉冲放电等离子体烟气治理技术是利用高压脉冲电源产生的高能电子激活燃煤烟气中的氧气、水蒸气等生成活性物种OH，O，O3等，氧化烟气中的SO2和NOx，并加入氨作为中和剂，生成（NH4）2SO4和NH4NO3肥料的烟气综合治理技术。活化水蒸气／氨能有效地提高脱硫效率和降低能耗。     

等离子体中活性粒子分析及化学动力学机理

利用发射光谱测量技术分析了介质阻挡放电等离子体激励空气产生的主要活性粒子,利用零维等离子体动力学模型模拟了甲烷/空气中放电阶段主要活性粒子的演化规律,并通过敏感性与化学路径分析研究了O原子影响甲烷点火过程的化学动力学机理。研究表明:空气中介质阻挡放电等离子体主要产生N2和O2的激发态粒子,激发态粒子的数密度随着电压的增加而增大;激发态粒子经过一系列物理化学反应最终转化成若干自由基,其中O原子的摩尔分数最大;O原子缩短甲烷点火延迟时间一个量级,原因在于添加O原子后甲基(CH3)的氧化途径由自点火过程中的经O2直接氧化为CH3O和CH2O转变为经HO2和O原子氧化为CH3O和CH2O,由于后者的基元反应速率快,因而明显缩短了点火延迟时间。     

等离子体助燃旋流扩散火焰的光谱分析

介质阻挡放电(DBD)辅助燃烧是等离子体技术领域发展起来的新的应用途径.本文利用CCD相机及光谱仪记录并分析甲烷-空气旋流扩散燃烧火焰形态及特征光谱,研究了等离子体激励的助燃、稳燃机理,分析了不同激励方式对等离子激励效果的影响。实验结果表明,等离子体激励放电会产生大量的自由基及活性基团,如CH,OH,O~+,O原子的各激发态能级及N_2第一正带系等谱线,其中重点分析了加电前后及不同激励方式下O原子(3s~3S~0→3p~5P,λ=777.5 nm)及氮气第一正带系B~3Π_g→A~3∑_u~+粒子(振动带波长为λ=891.2 nm)发射光谱变化,由于氮原子与氧原子均为加速燃烧的重要活性粒子,这些基团的产生使得甲烷更容易发生一系列链式氧化反应。定常激励产生的活性粒子浓度大于未经过等离子体激励及非定常激励下所产生的活性粒子浓度;经过等离子体激励后火焰根部更靠近燃烧器喷嘴底部,说明等离子体激励产生的活性粒子加速了链式反应的进行,缩短了点火迟滞时间.     

Au_(38)团簇上小分子H_2O和O_2共同吸附的第一性原理研究

利用密度泛函理论(DFT)计算的方法,对O_2,H_2O单独吸附和共吸附在Au_(38)团簇上的吸附性质进行了结构,能量和电子分析.计算结果表明,O_2倾向于吸附在edge位,H_2O则倾向于吸附在top位.Au(100)表面较之Au(111)表面更有利于O_2,H_2O的吸附,这与实验结果相符合.H_2O和O_2共吸附研究表明,H_2O的存在促进了O_2的吸附.Mulliken和分态密度(PDOS)分析得出:在共吸附中,H_2O将部分电子转移给了O_2,促进了O_2的活化与解离,并生成了类似H_2O_2的中间态,从而为催化氧化反应提供了O活性物种.     

低温等离子体活化转化煤层甲烷机理的光谱诊断

为了探究低温等离子体活化转化煤层甲烷的机理,采用自制的介质阻挡放电实验系统对体积组成为CH440%、O212%、N248%的模拟煤层甲烷进行等离子体活化转化。采用色谱分析方法对煤层甲烷介质阻挡放电稳定产物进行分析,结果表明低温等离子体活化煤层甲烷的主要产物为CH3OH、CO和CO_2。采用发射光谱原位诊断技术在200~700 nm波长范围内研究了放电气体的发射光谱,检测到O·、CH·、C·、Hα、N2(A3Σ+U)等激发态物种。基于发射光谱原位诊断和气相色谱分析结果,对煤层甲烷活化转化的自由基反应过程进行了推断。同时,明晰了反应气中N2对煤层甲烷活化和主要产物的生成具有促进作用,即N2产生了存活时间更长的亚稳态离子,该亚稳态离子将能量传递给反应气中的O2和CH4,进而加速了煤层甲烷的活化和稳定产物的生成。     

光谱诊断冷等离子体作用下甲烷转化机理的初步研究(英文)

冷等离子体是甲烷无氧活化制C2烃较为有效的技术手段之一,由于等离子体反应体系的复杂性,甲烷无氧活化制C2烃反应机理及过程尚不十分清楚。本文采用发射光谱原位诊断技术对冷等离子体作用下甲烷无氧活化制C2烃反应中若干激发态物种进行诊断研究,在250nm～670nm波长范围内检测到下列激发态物种:CH、C和C2。依据激发态物种检测结果、气相色谱反应产物分析结果及等离子体特性,推断了等离子体作用下甲烷无氧活化制C2烃的自由基反应历程。     

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研究了氮氧源大气压等离子体射流对表面大肠杆菌灭活作用,分析了氮氧源大气压等离子体射流的光谱性质.结果表明,在放电电压为6.8kV,气体流速为4L?min-1,处理3min时,氮氧比为1:4的大气压等离子体射流对大肠杆菌的灭活率达到98.4%,接近氧气源大气压等离子体射流灭菌效果.通过大气压等离子体射流发射光谱(OES)分析了氮氧源大气压等离子体射流中活性物质,进而解释大肠杆菌微生物灭活机理,认为NO-γ、OI、·OH等活性物质在表面大肠杆菌灭活过程中起到了重要作用.这将为大气压氮氧等离子体射流在环境卫生、微生物灭活等方面的应用研究提供实验基础和技术支持.     

陶瓷表面放电光泵浦源放电特性研究

为了提高表面放电光泵浦源的寿命,以Al_2O_3陶瓷作为放电基板,研制了分段表面放电光泵浦源。基于放电电压和电流波形,详细研究了泵浦源的放电周期,放电通道电阻,能量沉积效率和等离子体功率密度。发现泵浦源的放电周期、放电通道电阻和能量沉积效率均随放电间隙长度和混合气体气压的增大而变大,随充电电压的增加而减小;而等离子体功率密度主要取决于充电电压和放电间隙长度,基本不随混合气体气压的改变而变化。在充电电压为26. 8 kV,气压为100 kPa,放电间隙长8 cm的条件下,泵浦源的能量沉积效率约为82%,等离子体功率密度达到了9. 36 MW/cm。实验研究表明:Al_2O_3陶瓷表面放电光泵浦源具有良好的放电特性,较同等条件下聚四氟乙烯表面放电光泵浦源的等离子体功率密度更高,可产生更强的真空紫外辐射,辐射亮度温度大于23 kK。Al_2O_3陶瓷表面放电光泵浦源适用于光泵浦XeF_2气体形成大功率XeF(C-A)蓝绿激光。     

A cold thermionically emitting dusty air plasma formed by radiativeheating of graphite particulates

Formation of an atmospheric pressure dusty air plasma is explored experimentally in this paper. The plasma is created by seeding an air flow with graphite particles and irradiating the particulates with a focused CO₂ laser beam. The graphite particles are, thus, heated to thermionically emitting temperatures, and average particle temperatures and average particle number densities are measured. The presence of charges is inferred both from these measured quantities using a simple theoretical transient model, and experimentally by applying a dc bias across the irradiated region. It is found that an electron density of ~6.7 × 10⁵ cm^-3 (6.7 × 10¹¹ m^-3) can be produced at steady state in the presence of O₂. This value can be increased to 3.6 × 10⁷ cm^-3 (3.6 × 10¹³ m ^-1) in the ideal case where an electron attachment to O₂ is suppressed and where a lower work function particulate is used     

基于过氧化氢-桑色素化学发光体系的硫化物检测

在pH=9～10范围内,过氧化氢与桑色素溶液混合后可产生较弱的化学发光,表面活性剂十六烷基三甲基溴化铵(CTMAB)和S2-对该体系化学发光有较强的增敏作用,据此建立了H2O2-桑色素-CTMAB化学发光体系测定S2-的新方法,并对该体系的化学发光反应机理进行了研究.在最佳的实验条件下,S2-在(0.9～9.0)×10...     

Fe3O4磁性纳米颗粒的催化性能研究进展

综述了国内外这一领域科研工作者的研究成果,以紫外光谱（UV）和电化学传感器为主要手段阐述了Fe₃O₄MNPs对H₂O₂的催化作用并对Fe₃O₄MNPs利用其催化性质在H₂O₂的检测领域的进一步发展和应用进行了展望。     

Quantitative cleaning characterization of a lithium-fluoride iondiode

An ion source cleaning testbed was created to test plasma-cleaning techniques, and to provide quantitative data on plasma-cleaning protocols prior to implementation on the SABRE accelerator. The testbed was designed to resolve issues regarding the quantity of contaminants absorbed by the anode source (LiF), and the best cleaning methodology. A test chamber was devised containing a duplicate of the SABRE diode. Radio-frequency (RF) power was fed to the anode, which was isolated from ground and thus served as the plasma discharge electrode. RF plasma discharges in 1-3 mtorr of Ar with 10% O₂ were found to provide the best cleaning of the LiF surface. X-ray photoelectron spectroscopy (XPS) showed that the LiF could accrue dozens of monolayers of carbon just by sitting in a 2×10^-5 vacuum for 24 h. Tests of various discharge cleaning protocols indicated that 15 min of an Ar/O₂ discharge was sufficient to reduce this initial 13-45 monolayers of carbon impurities to 2-4 monolayers. Rapid recontamination of the LiF was also observed. Up to ten monolayers of carbon returned in 2 min after termination of the plasma discharge and subsequent pumping back to the 10^-5 torr range. Heating of the LiF also was found to provide anode cleaning. Application of heating combined with plasma cleaning provided the highest cleaning rates     

LaTiO高k栅介质Ge MOS电容电特性及Ti含量优化

采用共反应溅射法将Ti添加到La_2O_3中,制备了LaTiO/Ge金属-氧化物-半导体电容,并就Ti含量对器件电特性的影响进行了仔细研究.由于Ti-基氧化物具有极高的介电常数,LaTiO栅介质能够获得高k值;然而由于界面/近界面缺陷随着Ti含量的升高而增加,添加Ti使界面质量恶化,进而使栅极漏电流增大、器件可靠性降低.因此,为了在器件电特性之间实现协调,对Ti含量进行优化显得尤为重要.就所研究的Ti/La_2O_3比率而言,18.4%的Ti/La_2O_3比率最合适.该比率导致器件呈现出高k值(22.7)、低D_(it)(5.5×10~(11)eV~(-1)·cm~(-2))、可接受的J_g(V_g=1V,J_g=7.1×10~(-3)A·cm~(-2))和良好的器件可靠性.     

Effect of P2O5 addition on the structural and spectroscopic properties of sodium aluminosilicate glass

The structural and spectroscopic properties of Na₂O-Al₂O₃-SiO₂-xP₂O₅ glasses（x = 0 to 7 mol%） are investigated.Both Raman and IR spectra reveal that discrete phosphate species([PO₄]^-3,[PO3O_1/2]^-2) with low polymerization degree can be formed in the silicate glass.These phosphate structures scavenge non-bridging oxygen ions and cations from the silicate network,resulting in an increase of the glass transition temperature.According to the Judd-Ofelt intensity parameters（Ω₂,Ω₄,Ω₆） of Er³⁺.the asymmetry of local environment around Er³⁺ becomes higher,and the bond covalency between Er³⁺ and O^2-decreases after P2O5 is introduced.In the emission spectra,photo-luminescence intensity increases with increasing P₂O₅ concentration and the spectra are inhornogeneously broadened,revealing that the ligand electric field around Er³⁺ is dramatically changed,and the glass matrix becomes disordered.     

低温等离子体分解N2/O2/NO气氛中NO试验研究

利用自行设计的介质阻挡放电型低温等离子体反应器,研究了NO初始浓度、O₂初始浓度、放电功率、电源频率等因素对NTP转化N₂/O₂/NO气氛中NO的影响规律。研究发现,NO去除率随功率增大而升高,到达一最大值后随功率增大而降低;NO去除率随O₂初始浓度增加而降低,随NO初始浓度增大而减小。相同放电功率下,同一组分中NO去除率随电源频率的增加而降低,因此相同放电功率下降低电源频率可提高NO去除率。O₂初始浓度不高于5%时,NO_x大部分为NO,NO₂和O₃浓度均随放电功率增大而降低,NO₂、O₃生成量随O₂初始浓度升高而增多。     

Electrical conductivity and defect structure of Mg-doped Cr2O3

The electrical conductivity of Cr₂O₃ nominally doped with 2 mol% MgO has been studied by the four point a.c. technique as a function of the oxygen activity (O₂ + Ar, CO + CO₂ and H₂ + H₂O) in the temperature range 400–1200 °C. It is concluded that Cr₂O₃ doped with MgO is an extrinsic conductor and that the dissolved Mg-dopant is compensated by the formation of electron holes at near atmospheric oxygen pressures and by oxygen vacancies (or possibly interstitial chromium ions) at highly reduced oxygen activities (in CO + CO₂ and H₂ + H₂O gas mixtures). In H₂ + H₂O mixtures Mg-doped chromia also dissolves hydrogen as protons and significantly affects the defect structure and electrical conductivity. The defect structure of the oxide under various conditions is discussed.     

O2/CO2气氛下循环流化床煤燃烧SO2排放

在热输入功率50 kW的循环流化床O₂/CO₂燃烧试验装置上研究燃煤SO₂排放特性及石灰石脱硫机理。结果发现,未添加石灰石时,O₂/CO₂气氛下SO₂排放量比相同O₂浓度的空气气氛下低;随着O₂浓度的升高,排放量升高。相同钙硫摩尔比下,O₂/CO₂气氛下石灰石的脱硫机理以直接脱硫为主,脱硫效率比空气气氛下高;随着O₂浓度的增加,石灰石脱硫效率提高。     

Effects of surface treatments and annealing on carbon-based molecular sieve membranes for gas separation

A new method in preparing carbon-based molecular sieve (CMS) membranes for gas separation has been proposed. Carbon-based films are deposited on porous Al₂O₃ disks using hexamethyldisiloxane (HMDSO) by remote inductively coupled plasma (ICP) chemical vapor deposition (CVD). After treating the film with ion bombardment and subsequent pyrolysis at a high temperature, carbon-based molecule sieve membranes can be obtained, exhibiting a very high H₂/N₂ selectivity around 100 and an extremely high permeance of H₂ around 1.5 × 10⁻⁶ mol m⁻² s⁻¹ Pa⁻¹ at 298 K. The O₂/N₂ selectivity could reach 5.4 with the O₂ permeance of 2 × 10⁻⁷ mol m⁻² s⁻¹ Pa⁻¹ at 423 K.

During surface treatments, HMDSO ions were found to be more effective than CH₄, Ar, O₂ and N₂ ions to improve the selectivity and permeance. Short and optimized surface treatment periods were required for high efficiency. Without pyrolysis, surface treatments alone greatly reduced the H₂ and N₂ permeances and had no effect on the selectivity. Besides, without any surface treatment, pyrolysis alone greatly increased the H₂ and N₂ permeances, but had no improvement on the selectivity, owing to the creation of large pores by desorption of carbon. A combination of surface treatment and pyrolysis is necessary for simultaneously enhancing the permeance and the selectivity of CMS membranes, very different from the conventional pore-plugging mechanism in typical CVD.