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101.
102.
Vibration Characteristics of Acoustically Levitated Object with Rigid and Elastic Reflectors
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Levitation stability is a crucial factor that influences acoustic levitation capability. We present two sample-including models for a single-axis acoustic levitator with either a rigid or elastic reflector. Numerical analysis shows that, with the rigid reflector, both the decay time from initial disturbance and the vibration amplitude increase with sample density, which is unfavorable for levitation stability. However, with the elastic reflector, the decay time and the vibration amplitude are greatly reduced by choosing appropriate parameters of the reflector. Experimental results agree well with theoretical predictions, indicating that levitation stability can be remarkably enhanced by replacing the rigid reflector with an elastic reflector. 相似文献
103.
The reactions of CoCl2·6H2O, dppm (bis(diphenylphosphino)methane) and TCNQ (7,7,8,8-tetracyanoquinodimethane), with different ratios of the components, provided three new compounds, [Co(dppmdo)3][TCNQ]21 (dppmdo = P,P′-dioxo-bis(diphenylphosphinyl)methane), [Co(dppmdo)3][(μ-TCNQ)-CoCl3] 2, and [Co(dppmdo)3][(μ-DCBE)-CoCl3] 3 (DCBE = p-dicyanomethyl-benzoic ethyl ester). These products were characterized by IR, UV–Vis and UV–Vis-NIR spectra, X-ray crystallography, magnetic susceptibility measurements and cyclic voltammograms. 1 and 2 reveal low-energy transitions in the near-infrared region, which can be attributed to intra-ligand transitions involving radical anions (TCNQ/TCNQ−). It is interesting to note that, except for the redox potentials which are anodically shifted, indicating that it is easier to reduce TCNQ in 1 and 2 than the free TCNQ molecule, the electrochemistry of compounds 1 and 2 resemble that of the independent organic acceptor TCNQ. The magnetic properties suggest that an amount of electron transfer has occurred from the CoII complex, [Co(dppmdo)3]2+, to the TCNQ− anions in 1; an amount of electron transfer also has occurred from the CoII cation to the TCNQ− anion via a cyanide-bridge in 2; there is a mixture of spin transition of CoII ions and antiferromagnetic coupling between CoII ions in 3. 相似文献
104.
The vapor heat capacities of acetic acid, propionic acid, n-butyric acid at various temperatures under atmospheric pressure were measured with a multicomponent vapor flow calorimeter. The results show that the vapor heat capacities of carboxylic acids are much larger than those of the ideal gases at the same temperature and that the vapor heat capacities decrease with increasing temperature. The effect of association in the vapor phase on the vapor heat capacity was studied. 相似文献
105.
[(PbCl2)0.55(PbO)0.45]1—x(KCl)x系离子导电性研究 总被引:1,自引:0,他引:1
对POGI_2-PbO体系进行KGl掺杂改性研究.实验表明少量KGl掺杂试样可直接在空气中烧结制备.对[(PbCl_2)_(0.55)(PbO)_(0.45)]_(1-x)(KCl)_x(x=0~0.30)的试样进行了电学测试.并做了X射线物相鉴定以确定高电导体系的主相.对0.05≤x≤0.22之间的体系电导率低谷现象进行了解释. 相似文献
106.
铝掺杂针铁矿的制备、表征及吸附氟的特性 总被引:1,自引:0,他引:1
水热条件下制备了针铁矿(Goe)和几种铝掺杂针铁矿(Goe-Al_(0.1),Goe-Al_(0.2)和Goe-Al_(0.4)),用X射线衍射(XRD)、扫描电镜(SEM)、氮气物理性吸附、酸碱滴定等手段对样品进行了表征,并研究了它们对氟离子的吸附特性。结果表明,随着铝掺杂量的增加,铝掺杂针铁矿的结晶度不断减弱、颗粒的长度不断减小。4种样品的微孔表面积、孔体积和表面分形度都表现为GoeGoeAl0.1Goe-Al_(0.2)Goe-Al_(0.4),而孔径分布表现为相反的顺序。Goe、Goe-Al_(0.1)、Goe-Al_(0.2)和Goe-Al_(0.4)的电荷零点(PZC)分别为8.2、8.3、8.5和8.7,pH=5.0时它们的表面电荷量分别为0.66、0.83、1.03和1.19 mmol·g~(-1)。准二级动力学模型适合描述4种样品对氟的吸附动力学过程,表明化学吸附是主要作用机制。一位Langmuir模型可较好的拟合等温吸附数据(R2为0.967~0.981),二位Langmuir模型对等温吸附数据的拟合度更高(R2为0.982~0.995),而Freundlich模型的拟合度较低(R2为0.877~0.912)。初始pH=5.0时,Goe、Goe-Al_(0.1)、Goe-Al_(0.2)和Goe-Al_(0.4)对氟的最大吸附容量分别为8.83、10.24、11.72和12.86 mg·g~(-1)。可见,铝掺杂针铁矿对土-水环境中氟的吸附容量高于纯针铁矿。 相似文献
107.
The phase transition of the 5-state dock model has been studied by standard variationalcumulant expansion (VCE) method. We calculated the fiee energy (F) and the internal energy (E) to the fourth order approximation and the specific heat (C) to the third order approximation with the trial action of one variational parameter. The position of the phase transition point given above is in agreement with the results of the Monte Carlo (MC). We also calculated the model to the third order approximation with the trial action of two variational parameters. The comparison of the results for one variational parameter with that for two is given. From this, we can see how the choice of the trial action affects the result and the trial action must be equivalent to the action of the system. All above has shown that the VCE is convergent in the calculation of the 5-state clock model. 相似文献
108.
采用物理喷束淀积技术,制备了聚乙烯咔唑(PVK)与富勒烯C60的组合薄膜系列,通过测量这些组合膜和纯膜的稳态和瞬态光生电压,研究了组合膜光诱导电荷转移性质.发现PVK/C60双层组合膜的光生电压比纯PVK薄膜和PVK与C60均匀混合膜有5个数量级的增强,比纯C60薄膜也有大于一个数量级的增强.实验结果证明:在光激发下,组合膜中两种分子间发生了快速的电子转移,并在PVK/C60界面处产生有效的电荷分离,导致PVK/C60双层组合膜光生电压的显著增强.并通过与ITO/C60/Al结构的瞬态光生电压响应的比较,
关键词: 相似文献
109.
Certain colloidal metals such as.silver (Ag), gold (Au) and copper, (Cu), when properly or assembled, display remarkable enhancement effect to the Raman scattering cross section of adsorbed molecules. This surface-enhanced Raman scattering (SERS) phenomenon has found wide applications in the study of interfacial chemical processes and is a potentially non-invasive technique in molecule-specific analysis. However, the SERS activity of metal colloids depends sensitively on both the synthetic method and the aggregation and assembly procedure, making it difficult to develop SERS into a reliable and quantitative analytical technique. To solve this problem, one needs to develop a substrate with a well-defined adsorption area and SERS activity. One approach to achieve this goal is to assemble a monolayer of uniform colloidal metals onto a well-defined secondary substrate. Here we report our effort in assembling monolayers of uniform Au nanoparticles on the well-defined optical-inactive microparticles in a layer-by-layer (LbL) manner and the use of such assembly as SERS-active substrate. 相似文献
110.
一个对称萘酞菁的LB膜及其二阶非线性光学性质的研究 总被引:1,自引:0,他引:1
用水平提拉法制备了四叔丁基萘酞菁锌的LB膜。利用表面压-面积曲线、紫外-可见吸收光谱、小角X-射线衍射等表征了LB膜的结构,结果表明该化合物可以形成较高质量的具有很好层状结构的多层LB膜,在膜中分子大环平面垂直于基片平面并且以分子平面并不完全重合的H-聚集体存在。采用透射SHG方法测量了相应LB膜的二阶非线性光学性质,结果显示在实验条件下该化合物LB膜的宏观二阶非线性系数以及分子超极化率分别为X 相似文献