Balmer Hα,Hβ and Hγ Spectral Lines Intensities in High-Power RF Hydrogen Plasmas

Hα（Balmer-alpha）, Hβ （Balmer-beta） and Hγ （Balmer-gamma） spectral line inten- sities in atomic hydrogen plasma are investigated by using a high-power RF source. The intensities of the Hα, Hβ and Hγ spectral lines are detected by increasing the input power （0-6 kW） of ICPs （inductively coupled plasmas）. With the increase of net input power, the intensity of Hα im- proves rapidly （0-2 kW）, and then reaches its dynamic equilibrium; the intensities of Hβ can be divided into three processes： obvious increase （0-2 kW）, rapid increase （2-4 kW）, almost constant （4-6 kW）; while the intensities of Hγ increase very slowly. The energy levels of the excited hydro- gen atoms and the splitting energy levels produced by an obvious Stark effect play an important role in the results.     

Characterization of Crystalline Nanoparticles/Nanorods Synthesized by Atmospheric Plasma Enhanced Chemical Vapor Deposition of Perfluorohexane

A mass of nanoparticles/nanorods were formed on a simultaneously deposited gran- ular film by plasma enhanced chemical vapor deposition （PECVD） of perfluorohexane at atmo- spheric pressure without any catalysts or templates. Scanning electron microscopy （SEM） and X-ray photoelectron spectroscopy （XPS） were used to characterize the morphology and the chem- ical compositions of nanoparticles. The average size of particles is about 100 nm and the length of synthesized nanorods is between 1 μm and 2.5/tm. The analyses of transmission electron microscopy （TEM）, high-resolution transmission electron microscopy （HRTEM）, selected area electron diffraction（SAED） and X-ray diffraction （XRD） reveals that the nanoparticles and nanorods are crystalline.     

The Gas Nucleation Process Study of Anatase TiO2 in Atmospheric Non-Thermal Plasma EnhancedChemical Vapor Deposition简

Abstract The gas phase nucleation process of anatase TiO2 in atmospheric non-thermal plasma enhanced chemical vapor deposition is studied. The particles synthesized in the plasma gas phase at different power density were collected outside of the reactor. The structure of the collected particles has been investigated by field scanning electron microscope （FESEM）, X-ray diffraction （XRD）, high resolution transmission electron microscopy （HRTEM） and selected area electron diffraction （SAED）. The analysis shows that uniform crystalline nuclei with average size of several nanometers have been formed in the scale of micro second through this reactive atmo- spheric plasma gas process. The crystallinity of the nanoparticles increases with power density. The high density of crystalline nanonuclei in the plasma gas phase and the low gas temperature are beneficial to the fast deposition of the 3D porous anatase TiO2 film.     

氨基羟基脲与HNO2氧化还原反应研究

研究了高氯酸介质中氨基羟基脲与HNO₂的还原反应动力学,其动力学方程式为－dc(HNO₂)/dt=kc(HNO2)c^0.25(HSC)c^0.42(H⁺),在1.0℃时反应速率常数k＝(1.05±0.05)(mol/L)^－0.67•s^-1,活化能为(73.1±3.0)kJ/mol。研究了氨基羟基脲浓度、H⁺浓度、硝酸根浓度对氨基羟基脲与HNO₂还原反应速率的影响。结果表明：增加氨基羟基脲浓度和H⁺浓度,HNO₂还原速度增加;高氯酸根浓度对氨基羟基脲还原HNO₂速率基本无影响。     

Comparison of Sterilizing Effect of Nonequilibrium Atmospheric-Pressure He/O2 and Ar/O2 Plasma Jets

The sterilizing effect of the non-equilibrium atmospheric pressure plasma jet by applying it to the Bacillus subtilis spores is invesigated. A stable glow discharge in argon or helium gas fed with active gas （oxygen）, was generated in the coaxial cylindrical reactor powered by the radio-frequency power supply at atmospheric pressure. The experimental results indicated that the efficiency of killing spores by making use of an Ar/O2 plasma jet was much better than with a He/O2 plasma jet. The decimal reduction value of Ar/O2 and He/O2 plasma jets under the same experimental conditions was 4.5 seconds and 125 seconds, respectively. It was found that there exists an optimum oxygen concentration for a certain input power, at which the sterilization efficiency reaches a maximum value. It is believed that the oxygen radicals are generated most efficiently under this optimum condition.     

层状金属硫化物硫化锡钾的制备及其对Sr2+的吸附性能研究

本文用水热法合成了硫化锡钾（KSnS），利用扫描电镜（SEM）、X射线衍射（XRD）仪等对KSnS的形貌和组成进行了表征分析，并通过静态吸附实验分别研究了pH值、接触时间、共存离子和Sr²⁺初始浓度对KSnS吸附Sr²⁺的影响。结果表明，在40 ℃、pH=7.25、Sr²⁺初始浓度为5.5 mg/L的条件下，KSnS对Sr²⁺的吸附平衡时间约为35 min，Sr²⁺去除率为99.62%。吸附反应可操作pH值范围较宽，52+去除率保持在80%以上。溶液中含有K⁺、Na⁺、Ca²⁺和Mg²⁺等共存离子时，二价离子的干扰大于一价离子。KSnS对Sr²⁺的吸附动力学行为可用准二级动力学方程描述，吸附过程属于化学吸附。通过Weber-Morris模型和Boyd模型分析可知，液膜扩散是主导吸附速率的步骤。     

ESR法研究Pt催化N2H4分解机制

采用电子自旋共振谱（ESR）法，研究了酸性条件下•NH₂的转化，HClO₄体系下反应时间对溶液中自由基产生的影响、pH值对N₂H₄断键的影响以及HNO₃中N是否对溶液中的•NH₂有贡献，确定了Pt催化N₂H₄分解的反应机理。结果表明：在酸性条件下•NH₂被DMPO捕捉时反应式为•NH⁺₃+HO-H+DMPO=NH⁺₄+DMPO(•OH)，硝酸在Pt催化N₂H₄体系中不会发生断键产生•NH₂，所产生的•NH₂是由N₂H₄断键形成的；在HClO₄体系中，随着Pt催化N₂H₄反应时间的延长，N₂H₄中N-N断键的趋势逐渐减小，N-H断键的趋势逐渐增大；随pH值的增大，N₂H₄中N-N断键的速率先快速减小，pH>3后缓慢增大；Pt催化N₂H₄分解反应中N-N断键和N-H断键两种方式共存，但N-N断键占优；反应体系中N₂H₄与H^＋浓度之比决定了N-N断键生成•NH₂的速率，而•NH₂与H^＋的浓度又决定了•NH₂转化成产物的速率，这两方面共同决定了N₂H₄分解的速率。     

Simultaneous Oxidization of NOx and SO2 by a New Non-thermal Plasma Reactor Enhanced by Catalyst and Additive

The non-thermal plasma as one of the most promising technologies for removing NOx and SO2 has attrm~ted much attention. In this study, a new plasma reactor combined with catalyst and additive was developed to effectively oxidize and remove NOx and SO2 in the flue gas. The experimental results showed that TiO2 could improve the oxidation efficiency of SO2 in the case of applying plasma while having a negative effect on the oxidation process of NO and NOx. With the addition of NH3, the oxidation rates of NOx, NO and SO2 were slightly increased. However, the effect of adding NH3 on NOx oxidation was negative when the temperature was above 200℃.     

Modification of Ni/SiO2 Catalysts by Means of a Novel Plasma Technology

Atmospheric high frequency cold plasma jet was applied to modify Ni/SiO2 catalysts. The catalysts prepared by two different methods with plasma jet were compared with conventional catalysts. BET, XRD, H2-TPD and high-resolution transmission electron microscopy （HRTEM） were used to characterize these catalysts. The results showed that the catalyst prepared with plasma jet had higher nickel dispersion, larger specific surface area and smaller nickel particle size, about 5 nanometres. Detailed analyses revealed that improved structure and characteristic of the plasma catalyst were benefited from the large amount of hydrogen atoms in the plasma jet, by which the catalyst reduction can be easily achieved in shorter period of time at lower temperature, thus avoiding sintering and conglomeration of the active particles and the support. The activity of catalysts was investigated in the methane reforming with CO2. It is shown that the conversions of CH4 and CO2, the yields of H2 and CO were all significantly increased for the plasma catalysts.     

Numerical Investigation of Flow Fields in Inductively Coupled Plasma Wind Tunnels

Numerical simulations of 10 kW and 110 kW inductively coupled plasma （ICP） wind tunnels were carried out to study physical properties of the flow inside the ICP torch and vacuum chamber with air as tile working gas. Two-dimensional compressible axisymmetric Navier- Stokes （N-S） equations that took into account 11 species and 49 chemical reactions of air, were solved. A heat source model was used to describe the heating phenomenon instead of solving the electromagnetic equations. In the vacuum chamber, a four-temperature model was coupled with N-S equations. Numerical results for tile 10 kW ICP wind tunnel are presented and discussed in detail as a representative case. It was found that the plasma flow in the vacuum chamber tended to be in local thermoehemical equilibrium. To study the influence of operation conditions on the flow field, simulations were carried out for different chamber pressures and/or input powers. The computational results for the above two ICP wind tunnels were compared with corresponding experimental data. The computational and experimental results agree well, therefore the flow fields of ICP wind tunnels can be clearly understood.     

Study of chemical kinetics on labeling of 99mTc-N-ethyl-N2S2-Memantine

In this work,a calculation method of chemical kinetics was established for labeling reaction of 99mTc-N-ethyl-N2S2-memantine,a potential NMDA receptor imaging agent prepared in our laboratory.Four groups of vials (3 vials per group) were added with 0.02 mL (1 mg/mL) N-ethyl-N2S2Memantine,0.08 mL (40 mg/mL) GH,0.05 mL (10 mg/mL) EDTA-2Na,0.035 mL (2 mg/mL) SnF2,0.8 mL phosphate buffer(1mol/L,pH 6.5) and 37 MBq Na99mTcO4.The vials were incubated at 70℃,80℃,90℃ or 100℃.Samples were taken with capillary from the vials at 2,5,10,20,30,40 and 60min.Labeling yields were determined by TLC.Order of reaction n,rate constant k,activation energy Ea and half life t1/2 of labeling reaction were calculated with the kinetics software we compiled.Mean labeling yields of 99m Tc-N-ethyl-N2S2-memantine at 2,5,10,20,30,40 and 60min were (1) 13.5,15.7,34.0,64.8,81.9,91.4 and 95.4 at 70℃;(2) 13.2,20.5,40.1,70.0,88.2,94.5 and 95.6 at 80℃;(3) 15.6,22.9,43.7,74.3,87.2,93.4 and 96.1 at 90℃;and (4) 20.5,25.8,45.3,81.1,92.2,95.6 and 96.0 at 100℃.The other parameters were;n =1;k=0.053,0.061,0.063 and 0.076 L/min at 70℃,80℃,90℃ and 100℃,respectively;Ea=12.38 kJ/L;t1/2=13.11,11.45,11.05 and 9.07min at 70℃,80℃,90℃ and 100℃,respectively.The mean labeling yield increased with temperature and time,optimized at 100℃ and 40-60min.The concentration of 99mTc-N-ethyl-N2S2-Memantine was larger than that of Na99mTcO4,so n=1.The k increased with reaction,hence the accelerated reaction rate at higher temperatures.The labeling reaction was not so difficult because of the low Ea.The t1/2 decreased with increasing reaction temperature,hence the acceleration of labeling reaction.     

Synthesis of a Large Diamond Crystal with a Smooth （100） Facet at its Top Through MPCVD

A large diamond crystal up to 500μm in diameter with a smooth(100)facet at its top has been synthesized on Mo substrate through microwave plasma chemical vapor deposition(MPCVD).Its morphology and quality were characterized by scanning electron microscopy(SEM),and the growth mechanism was roughly illustrated from both macroscopic and microscopic viewpoints.It was found that morphological instabilities are a major factor resulting in synthesis of large diamond crystals,moreover,high microwave power density(MPD),high CH4 concentrations,high pressure,high substrate surface temperature and the addition of a small amount of O2 were also necessary for the synthesis of large diamond crystals.     

Fabrication of Titanium Dioxide Thin Films by DBD-CVD Under Atmosphere

Titanium dioxide films were firstly deposited on glass substrate by DBD-CVD （dielectric barrier discharge enhanced chemical vapor deposition） technique. The structure of the films was investigated by X-ray diffraction （XRD）, scanning electron microscopy （SEM）. TiO2 films deposited under atmosphere pressure show preferred orientation, and exhibit columnar-like structure, while TiO2 films deposited under low gas pressure show no preferred orientation. The columnar-like structure with preferred orientation exhibits higher photocatalytic efficiency, since the columnar structure has larger surface area. However, it contributes little to the improvement of hydrophilicity. DBD-CVD is an alternative method to prepare photocatalytic TiO2 for its well-controllable property.     

IMF production and symmetry energy in heavy ion collisions near Fermi energy

The symmetry energy at the time of the production of intermediate mass fragments （IMFs） is studied using experimentally observed IMF multiplicities combined with quantum statistical model calculations （QSM of Hahn and Stfcker）. The ratios of difference in chemical potentials between neutrons and protons relative to the temperature,（μt- μp） /T, and the double ratio temperature, T, were extracted experimentally in the reactions of 64＇7~Zn, 64Ni＋58＇64Ni, 112＇124Sn, 197Au, 232Th at 40A MeV. The extracted （μt- μp） / T scales linearly with Jwv, where fi~v is the asymmetry parameter, （N-Z）/A, of the emitting source and （μt- μp） / T = （11.1 ＋ 1.4）rNN -- 0.21 was derived. The experimentally extracted （μt-μp）/T and the double ratio temperatures are compared with those from the QSM calculations. The temperatures, T, and densities, p, extracted from the （μn - μp） / T values agreed with those from the double ratio thermometer which used the yield ratios of d, t, h and a particles. However the two analyses of the differential chemical potential analysis and the initial temperature analysis end up almost identical relation between T and p. T=5.25±0.75 MeV is evaluated from the （μn -μp） / T analysis, but no density determination was possible. From the extracted T value, the symmetry energy coefficient Esym=14.6±3.5 MeV is determined for the emitting source of T=5.25±0.75 MeV.     

氨基羟基脲与Pu(Ⅳ)的还原动力学研究

研究了氨基羟基脲(HSC)与Pu(Ⅳ)的还原反应动力学,其动力学方程式为：-d_c（Pu(Ⅳ)）/d_t=kc（Pu(Ⅳ））c^1.06（HSC）c^-0.43（H⁺）c^-0.58（NO₃^-）,在22.1℃时反应速率常数k＝(11.8±1.1)（mol/L）^-0.046•s^-1,活化能为(71.0±1.0)kJ/mol。研究了氨基羟基脲浓度、H⁺浓度、硝酸根浓度、Fe³⁺浓度、UO₂²⁺浓度对氨基羟基脲与Pu(Ⅳ)还原反应速率的影响,增加氨基羟基脲浓度,降低H⁺浓度、硝酸根浓度,Pu(Ⅳ)还原速度增加;UO₂²⁺浓度和Fe³⁺浓度对Pu(Ⅳ)还原速度基本无影响。     

热-水-力-化学耦合作用下Ca0.86Nd0.14Ti0.86Al0.14SiO5固溶体的化学稳定性

以CaCO₃、Nd₂O₃、TiO₂、SiO₂、Al₂O₃为原料,用固相法制备掺钕榍石固溶体（Ca_0.86Nd_0.14Ti_0.86Al_0.14SiO₅）。采用PCT法进行浸泡实验,借助X射线衍射（XRD）、扫描电镜（SEM）、电感耦合等离子体发射光谱（ICP-OES）等分析手段,研究掺钕榍石固溶体在热 水 力 化学（THMC）耦合作用下的化学稳定性。结果表明,在pH值为5～9、温度150～200 ℃、压强0.476～1.554 MPa的耦合作用下,Ca_0.86Nd_0.14Ti_0.86Al_0.14SiO₅固溶体具有良好的化学稳定性;pH值、温度（压力）对Ca_0.86Nd_0.14Ti_0.86Al_0.14SiO₅固溶体中Si⁴⁺、Al³⁺、Nd³⁺的归一化浸出率无明显影响;Ca²⁺在200 ℃（1 554 MPa）时的抗浸出性能较150 ℃时的好;在浸泡初期（1～21 d）Ca²⁺在pH值为9时的抗浸出性能优于pH值为5和7时的,浸泡后期（28、42 d）3种溶液中固溶体的Ca²⁺抗浸出性能趋于一致;Ti⁴⁺在pH值为9时的抗浸出性能较pH值为5和7时的好。     

Yield of H2O2in Gas-Liquid Phase with Pulsed DBD简

Electric discharge in water can generate a large number of oxidants such as ozone, hydrogen peroxide and hydroxyl radicals. In this paper, a non-thermal plasma processing system was established by means of pulsed dielectric barrier discharge in gas-liquid phase. The electrodes of discharge reactor were staggered. The yield of H2O2 was enhanced after discharge. The effects of discharge time, discharge voltage, frequency, initial pH value, and feed gas were investigated. The concentration of hydrogen peroxide and ozone was measured after discharge. The experimental results were fully analyzed. The chemical reaction equations in water were given as much as possible. At last, the water containing Rhodamine B was tested in this system. The degradation rate came to 94.22% in 30 min.     

Dynamic Characteristics of SF_6-N_2-CO_2 Gas Mixtures in DC Discharge Process

Dynamic characteristics of discharge particles are described within the framework of a two-dimensional photoionization-hydrodynamic numerical model for the discharge process of SF6-N2-CO2 gas mixtures at atmospheric pressure, under a uniform DC applied field. The finite difference flux corrected transport （FD-FCT） algorithm is used in the numerical implementation for improving the accuracy and efficiency. Then the tempo-spatial distributions of the gap space electric field and electron velocity are calculated from the microscopic mechanism, and the dynamic behaviors of charged particles are obtained in detail. Meanwhile, the tempo-spatial critical point of the avalanche-to-streamer in this model is discovered, and several microscopic parameters are also investigated. The results showed that the entire gap discharge process can be divided into two phases of avalanche and streamer according to Raether-Meek criterion; the electron density within the discharge channel is lower compared to that of positive and negative ions; space charge effect is a dominant factor for the distortion of spatial electric field, making the discharge channel expand toward both electrodes faster; photoionization provides seed electrons for a secondary electron avalanche, promoting the formation and development speed of the streamer.     

Calculation of Electron Swarm Parameters of SF6/N2 in a Uniform Field Using an Improved Monte Carlo Collision Simulation Method

The electron swarm parameters of SF6/N2 are calculated in the present study using an improved Monte Carlo collision simulation method （MCS）. And some improved sampling techniques are also adopted. The simulation results show that the improved simulation method can provide more accurate results.     

Formation of U2C3 in the reaction of UC2 with UO2

The formation of U₂C₃ by the reaction of UC₂ with UO₂ has been studied by chemical and X-ray analyses at temperatures between 1400 and 1700 °C in vacuo. The reaction is represented by 7 UC₂ + UO₂ → 4 U₂C₃ + 2 CO.