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161.
ZHOU Liuzhu ZHU Yuan GUO Xiaoyong ZHAO Wenwu ZHENG Haiyang Gu Xuejun FANG Li ZHANG Weijun 《中国科学G辑(英文版)》2006,49(2):187-194
Single aerosol particles were measured by matrix-assisted laser desorption/ionization (MALDI) with an aerosol time-of-flight
mass spectrometer (ATOFMS). The inlet to the ATOFMS was coupled with an evaporation/condensation flow cell that allowed matrix
addition by condensation onto the particles. The coated particles entered the ion source through three-stage differentially
pumped capillary inlet and were then ionized by a focused 266 nm Nd:YAG laser. The mass spectra and aerodynamic size of the
single particles can be obtained simultaneously. The on-line matrix addition technique makes it possible to identify biological
aerosols in real-time. 相似文献
162.
用密度泛函B3LYP方法研究了过渡金属钐类卡宾与乙烯的环丙烷化反应的机理。对三种不同的钐的SS试剂CH_3SmCH_2X(其中X=Cl、Br和Ⅰ)分别和CH_2CH_2反应的各反应物、中间体、过渡态和产物构型的全部结构几何参数进行了优化,用内禀反应坐标(IRC)计算和频率分析方法,对过渡态进行了验证。结果表明:CH_3SmCH_2X(其中X=Cl、Br和Ⅰ)与CH_2CH_2环丙烷化反应按亚甲基转移通道(通道A)和卡宾金属化通道(通道B)都可以进行,与锂类卡宾的反应机理相同,只是按亚甲基转移通道(通道A)进行反应较容易一些,而且此反应在较低的温度下就可以发生。 相似文献
163.
在CH_2~+体系的电子基态势能面上运用准经典轨线方法,研究了当碰撞能E=500 me V时,反应物分子的振动激发对H(~2S)+CH~+(X~1Σ~+)→C+(~2P)+H_2(X1_gΣ~+)反应的反应概率、反应截面和立体动力学性质的影响.分别计算了两矢量相关k-j′的P(θ_r)分布,三矢量相关k-k′-j′的P(φr)分布以及反应产物的四个极化微分截面.结果表明,产物分子转动角动量不仅在Y轴方向有取向效应,还定于Y轴的正方向.并且发现,随着振动量子数的增加,对反应体系产物分布的影响就越明显. 相似文献
164.
Yolk–Shell‐Structured Cu/Fe@γ‐Fe2O3 Nanoparticles Loaded Graphitic Porous Carbon for the Oxygen Reduction Reaction 下载免费PDF全文
Meiwen Wang Chao Su Martin Saunders Ji Liang Zongping Shao Shaobin Wang Jian Liu 《Particle & Particle Systems Characterization》2017,34(10)
Core–shell Cu/γ‐Fe2O3@C and yolk–shell‐structured Cu/Fe@γ‐Fe2O3@C particles are prepared by a facile synthesis method using copper oxide as template particles, resorcinol‐formaldehyde as the carbon precursor, and iron nitrate solution as the iron source via pyrolysis. With increasing carbonization temperature and time, solid γ‐Fe2O3 cores are formed and then transformed into Fe@γ‐Fe2O3 yolk–shell‐structured particles via Ostwald ripening under nitrogen gas flow. The composition variations are studied, and the formation mechanism is proposed for the generation of the hollow and yolk–shell‐structured metal and metal oxides. Moreover, highly graphitic carbons can be obtained by etching the metal and metal oxide nanoparticles through an acid treatment. The electrocatalytic activity for oxygen reduction reaction is investigated on Cu/γ‐Fe2O3@C, Cu/Fe@γ‐Fe2O3@C, and graphitic carbons, indicating comparable or even superior performance to other Fe‐based nanocatalysts. 相似文献
165.
采用非接触的色散荧光发射光谱和时间分辨光谱方法,在大气压条件下,对脉冲电晕放电脱除NO的化学反应动力学过程进行了实验研究。在该研究中,首先利用色散荧光发射光谱方法,得到纯NO气体脉冲电晕放电中各活性粒子的色散荧光谱,并对其进行归属,确定了各活性粒子的灵敏指纹跃迁谱线;在此基础上,通过测量NO气体放电过程中所产生的N+,O,N2及NO分子的灵敏指纹跃迁谱线的时间行为特性,研究脉冲电晕放电脱除NO的化学反应机理。实验结果表明:在脉冲电晕放电过程中,NO分子首先与高能电子发生非弹性电离碰撞,变成NO+离子,随后NO+离子发生解离反应,形成N+离子和O原子;N+离子在向阴极运动过程中与电子碰撞结合成激发态N原子,继而和其他激发态N原子结合成为激发态N2;而O原子则应与其它O原子结合成为O2。由此建立了大气压条件下纯NO气体脉冲电晕放电脱除NO的化学反应动力学模型。 相似文献
166.
高功率8 mm波辐照时,大小鼠均产生热应激反应,依次经历平静期、警戒期、相持期和衰竭期。鼠的热痛阈值温度为(43.1±1.8) ℃,这一阈值与鼠的质量、初始温度、辐照功率密度等无关。 辐照3 s时:辐照功率密度为3.5 W/cm2时体表温升为(8.4±1.0) ℃;辐照功率密度为7.0 W/cm2时温升为(21.1±3.0) ℃。实验还测定了警戒期持续时间,结果表明动物应激反应的剧烈程度与警戒期持续时间相关。建立了小鼠警戒期持续时间与小鼠体表面积、有效辐照面积、辐照功率密度之间的关系,并将这一实验结果推广到大鼠。 相似文献
167.
An efficient method for preparation of 4,6 or 5,6 disubstituted 3-aminopyridazines was easily carried out starting from easily available 4-bromo-pyridazine-3,6-dione, and using combination of both amination and Pd(0) cross-coupling reactions under microwave irradiation. 相似文献
168.
Proton and alpha particle spectra have been measured in the 12C+93Nb and 12C+58Ni reactions at E(12C)=40 and 50 MeV and in the 16O + 93Nb reaction at E(16O) =75 MeV. The spectra are compared with the statistical model calculations. The shapes of the calculated spectra are in
agreement with experimental data except for the alpha spectrum in the 12C + 93Nb reaction at 40 MeV. The observed evaporation bump is at ∼2 MeV lower energy compared to the calculated one. This discrepancy
could imply alpha particle emission from a deformed configuration before compound nucleus formation at this near Coulomb barrier
beam energy. 相似文献
169.
Dmitry Zemlyanov Balazs Aszalos-Kiss Detre Teschner Michael Hävecker Robert Schlögl Werner Unterberger Bernhard Klötzer 《Surface science》2006,600(5):983-994
The oxidation of the Pd(1 1 1) surface was studied by in situ XPS during heating and cooling in 3 × 10−3 mbar O2. A number of adsorbed/dissolved oxygen species were identified by in situ XPS, such as the two dimensional surface oxide (Pd5O4), the supersaturated Oads layer, dissolved oxygen and the R 12.2° surface structure.Exposure of the Pd(1 1 1) single crystal to 3 × 10−3 mbar O2 at 425 K led to formation of the 2D oxide phase, which was in equilibrium with a supersaturated Oads layer. The supersaturated Oads layer was characterized by the O 1s core level peak at 530.37 eV. The 2D oxide, Pd5O4, was characterized by two O 1s components at 528.92 eV and 529.52 eV and by two oxygen-induced Pd 3d5/2 components at 335.5 eV and 336.24 eV. During heating in 3 × 10−3 mbar O2 the supersaturated Oads layer disappeared whereas the fraction of the surface covered with the 2D oxide grew. The surface was completely covered with the 2D oxide between 600 K and 655 K. Depth profiling by photon energy variation confirmed the surface nature of the 2D oxide. The 2D oxide decomposed completely above 717 K. Diffusion of oxygen in the palladium bulk occurred at these temperatures. A substantial oxygen signal assigned to the dissolved species was detected even at 923 K. The dissolved oxygen was characterised by the O 1s core level peak at 528.98 eV. The “bulk” nature of the dissolved oxygen species was verified by depth profiling.During cooling in 3 × 10−3 mbar O2, the oxidised Pd2+ species appeared at 788 K whereas the 2D oxide decomposed at 717 K during heating. The surface oxidised states exhibited an inverse hysteresis. The oxidised palladium state observed during cooling was assigned to a new oxide phase, probably the R 12.2° structure. 相似文献
170.
Alain Adenier Eva Cabet-Deliry Sophie Griveau Florence Mercier Christine Vautrin-Ul 《Surface science》2006,600(21):4801-4812
This study investigates the spontaneous grafting of different para-substituted phenyl groups on carbon and metallic surfaces from diazonium salts solutions. Glassy carbon, nickel, zinc and iron plates were allowed to react with an acetonitrile solution of aryldiazonium tetrafluoroborate salt by simple dipping. The surfaces were characterized before and after their immersion by XPS and AFM to evidence the formation of a coating on the different materials. The results are indicative of the presence of substituted phenyl groups on all the investigated surfaces. This study also aims at correlating grafting efficiency with metal reactivities and diazonium salt electronic properties by means of AFM and FT-IRRAS. For this purpose, zinc and nickel were chosen due to their opposite reducing properties and two diazonium salts were selected with electron-donor or -withdrawing para-substituents. The results tend to indicate that redox properties of both partners (diazonium + metal) are of prime importance for grafting to occur. 相似文献