我国农民消费问题的分省面板协整模型分析

依据现代消费理论,在符合中国经济现实假设条件下,建立了我国农民消费问题的数理函数。使用1980-2006年的宏观消费数据,通过协整模型分析表明我国农民的边际消费倾向约为0.69;基于Hausman检验的固定效应模型的面板单位根和面板协整对我国30个省份分析结果表明边际消费倾向为0.7;变截距变斜率面板模型表明各省的长期自主消费和长期边际消费倾向差异显著,上海、江苏呈现双高特征,吉林、海南和西藏则呈现双低特征,其他省份则表现为自主消费和边际消费倾向两者此高彼低的特点。差异产生的原因在于消费习惯不同以及收入差异导致的"主动、被动"消费造成的结果,提出了为西部增收以促进消费良性循环的合理的政策建议。     

非参数固定效应Panel Data模型的统计推断

本文主要讨论了非参数固定效应Panel data模型的估计与检验问题,首先我们利用Profile最小二乘方法得到了固定效应与非参数部分的估计;接着基于比较原假设与备择假设下模型拟合的残差平方和的思想针对固定效应的检验问题构造了检验统计量,并给出了计算检验p-值的F分布逼近法。     

‘Model selection for generalized linear models with factor‐augmented predictors’

This paper considers generalized linear models in a data‐rich environment in which a large number of potentially useful explanatory variables are available. In particular, it deals with the case that the sample size and the number of explanatory variables are of similar sizes. We adopt the idea that the relevant information of explanatory variables concerning the dependent variable can be represented by a small number of common factors and investigate the issue of selecting the number of common factors while taking into account the effect of estimated regressors. We develop an information criterion under model mis‐specification for both the distributional and structural assumptions and show that the proposed criterion is a natural extension of the Akaike information criterion (AIC). Simulations and empirical data analysis demonstrate that the proposed new criterion outperforms the AIC and Bayesian information criterion. Copyright © 2009 John Wiley & Sons, Ltd.     

Preparation and adsorption properties of crosslinked polystyrene-supported low-generation diethanolamine-typed dendrimer for metal ions

Two novel chelating resins, polystyrene supported G1.0 diethanolamine-typed dendrimer (PS-DEA) and G2.0 diethanolamine-typed dendrimer (PS-(DEA)₂), were prepared by anchoring low-generations diethanolamine-typed dendrimer into crosslinked polystyrene in this paper. Fourier transform-infrared spectra (FTIR), scanning electron microscopy (SEM) and elemental analysis were employed to character their structures. The results of adsorption for metal ions showed that the resins had good adsorption capacities for Cu²⁺, Ag⁺ and Hg²⁺, especially PS-DEA for Cu²⁺. The adsorption kinetics and adsorption isotherms of PS-DEA for Cu²⁺ and PS-(DEA)₂ for Hg²⁺ were studied. The results showed that the adsorption kinetics of the two resins can be modeled by pseudo second-order rate equation wonderfully and Langmuir and Freundlich equations could well interpret the adsorption of PS-(DEA)₂ for Hg²⁺ and PS-DEA for Cu²⁺, respectively. The adsorption mechanism of the resins for Cu²⁺ was confirmed by X-ray photoelectron spectroscopy (XPS).     

New analytical procedure based on a cellulose bag and ionic exchanger with p-aminobenzoic acid groups for differentiation of labile and inert metal species in aquatic systems

A new procedure was developed for the in situ characterization of the lability of metal species in aquatic systems by using a system equipped with a diffusion membrane and cellulose organomodified with p-aminobenzoic acid groups (DM-Cell-PAB). To this end, the DM-Cell-PAB system was prepared by adding cellulose organomodified with p-aminobenzoic acid groups (Cell-PAB) to pre-purified cellulose bags. After the DM-Cell-PAB system was sealed, it was examined in the laboratory to evaluate the influence of complexation time, mass of exchanger, pH, metal ions (Cu, Cd, Fe, Mn, and Ni), and concentration of organic matter on the relative lability of metal species. It was found that the pH and kinetics strongly influence the process of metal complexation by the DM-Cell-PAB system. At all pH levels, Cd, Mn, and Ni showed lower complexation with Cell-PAB resin than Cu and Fe metals. Note that relative lability of metals complexed to aquatic humic substances (AHS) in the presence of Cell-PAB resin showed the following order: Cu≅Fe≫Ni>Mn=Cd. The results presented here also indicate that increasing the AHS concentration decreases the lability of metal species by shifting the equilibrium to AHS–metal complexes. Our results indicate that the system under study offers an interesting alternative that can be applied to in situ experiments for differentiation of labile and inert metal species in aquatic systems.     

中国高技术产业的技术创新影响因素:基于面板数据模型的实证检验

利用中国16个高技术行业的面板数据,对高技术行业的技术创新影响因素进行了实证分析,不仅研究了R&D投入对高技术行业技术创新的影响,还考虑了行业融资结构、外资企业研发的技术溢出效应、产权结构、企业规模以及市场集中度等因素的影响作用.     

Single-crystal micro/nanostructures and thin films of lamellar molybdenum oxide by solid-state pyrolysis of organometallic derivatives of a cyclotriphosphazene

The solid-state pyrolysis of organometallic derivatives of a cyclotriphosphazene is demonstrated to be a new, simple and versatile solid-state templating method for obtaining single-crystal micro- and nanocrystals of transition and valve metal oxides. The technique, when applied to Mo-containing organometallics N₃P₃[OC₆H₄CH₂CN·Mo(CO)₅]₆ and N₃P₃[OC₆H₄CH₂CN·Mo(CO)₄ py]₆, results in stand-alone and surface-deposited lamellar MoO₃ single crystals, as determined by electron and atomic force microscopies and X-ray diffraction. The size and morphology of the resulting crystals can be tuned by the composition of the precursor. X-ray photoelectron and infrared spectroscopies indicate that the deposition of highly lamellar MoO₃ directly on an oxidized (400 nm SiO₂) surface or (100) single-crystal silicon surfaces yields a layered uniphasic single-crystal film formed by cluster diffusion on the surface during pyrolysis of the metal-carbonyl derivatives. For MoO₃ in its layered form, this provides a new route to an important intercalation material for high energy density battery materials.     

Cu nanoparticles incorporated polypyrrole modified GCE for sensitive simultaneous determination of dopamine and uric acid

Cu nanoparticles have been electrochemically incorporated polypyrrole film that was used for modification of the glassy carbon electrode surface. The performance of the electrode has been characterized by cyclic voltammetry and atomic force microscopy. The electrode has shown high electrocatalytic activity towards the oxidation of dopamine (DA) and uric acid (UA) simultaneously in a phosphate buffer solution (pH 7.00). The electrocatalytic oxidation currents of UA and DA were found linearly related to concentration over the range 1 × 10⁻⁹ to 1 × 10⁻⁵ M for UA and 1 × 10⁻⁹ to 1 × 10⁻⁷ M for DA using DPVs method. The detection limits were determined as 8 × 10⁻¹⁰ M (s/n = 3) for UA and 8.5 × 10⁻¹⁰ M (s/n = 3) for DA at a signal-to-noise ratio of 3.     

激光诱导铝纳米膜熔化机理的分子动力学模拟

采用耦合一维双温模型的分子动力学方法研究了纳米级的铝膜在飞秒激光辐照下的熔化机制.这种方法不仅能够在原子水平上展现金属膜的各种微观行为,还能有效地描述金属膜的激光能量吸收、传递和金属电子热传导等过程.模拟结果表明,与其它金属相比,铝膜在飞秒激光辐照下的电子温度、晶格温度以及内部压力等呈现出不同的变化.铝膜在较高强度激光辐照下会很快发生全局一致的熔化,这与镍膜上下非均匀的熔化不同.并且由于铝的电子-声子耦合强度较高导致铝膜较镍膜和金膜熔化得更快.模拟结果显示,铝膜的熔化时间与实验测量的超快激光诱导的铝膜熔化时间一致.进而从理论上支持激光诱导的铝膜熔化是一个热力学熔化过程.     

NiCo2O4对H2O2在碱性溶液中电化学还原反应的催化行为

利用溶胶-凝胶法合成纳米NiCo2O4,并利用X射线衍射和透射电镜分析其结构和表面形貌. 结果表明NiCo2O4具有尖晶石结构, 平均粒径约为15 nm. 利用电势线性扫描和恒电势法测定了其对H2O2在碱性溶液中电化学还原反应的催化性能. 发现NiCo2O4对H2O2电化学还原具有高的催化活性和稳定性, 在H2O2浓度低于0.6 mol·L-1时, 其电化学还原反应主要通过直接还原途径进行. 以NiCo2O4为阴极催化剂的Al-H2O2半燃料电池在室温下的开路电压达1.6 V; 在1.0 mol·L-1 H2O2溶液中, 峰值功率密度达209 mW·cm-2, 此时电流密度为220 mA·cm-2.