A hierarchical porous carbon membrane from polyacrylonitrile/polyvinylpyrrolidone blending membranes:Preparation,characterization and electrochemical capacitive performance

Novel hierarchical porous carbon membranes were fabricated through a simple carbonization procedure of well-defined blending polymer membrane precursors containing the source of carbon polyacrylonitrile （PAN） and an additive of polyvinylpyrrolidone （PVP）, which was prepared using phase inversion method. The as-fabricated materials were further used as the active electrode materials for supercapacitors. The effects of PVP concentration in the casting solution on structure feature and electrochemical capacitive performance of the as-prepared carbon membranes were also studied in detail. As the electrode material for supercapacitor, a high specific capacitance of 278.0 F/g could be attained at a current of 5 mA/cm2 and about 92.90% capacity retention could be maintained after 2000 charge/discharge cycles in 2 mol/L KOH solution with a PVP concentration of 0.3 wt% in the casting solution. The facile hierarchical pore structure preparation method and the good electrochemical capacitive performance make the prepared carbon membrane particularly promising for use in supercapacitor.     

A highly efficient capillary electrophoresis-based method for size determination of water-soluble CdSe/ZnS core-shell quantum dots

This paper describes a highly efficient method for size determination of water-soluble CdSe/ZnS core-shell quantum dots (QDs) by capillary electrophoresis (CE) using polymer additive as sieving medium. The influence of some factors, such as kinds and concentrations of the sieving medium, pH, concentrations of the background electrolyte (BGE) and applied voltage, on the separation of QDs was investigated. Under the optimal separation conditions, four different sized QDs were successfully separated, and the relative standard deviation (RSD) of the migration times for these QDs was below 1.013%. In addition, an equation was fit by taking into account the correlation existing between the electrophoretic mobilities and the sizes of a set of QDs. The feasibility of this equation to measure the sizes of other QDs was confirmed by comparison with the sizes obtained by transmission electron microscopy (TEM) experiment. This work offers a novel method for size determination of QDs, and provides an important reference on the study of QDs based on CE.     

Effect of mobile phase anionic additives on selectivity,efficiency, and sample loading capacity of cationic drugs in reversed-phase liquid chromatography

In the present work, we study the effect of mobile phase anionic additive type and concentration on the selectivity, efficiency, and sample loading capacity of cationic drugs in reversed-phase liquid chromatography (RPLC). The type and concentration of an anionic additive are known to have a strong effect on the absolute retention of cations in RPLC; in contrast they have only a small effect on the selectivity of one cation relative to a second as seen here. This is mainly due to the similarity of the ion pair formation constants between the selected cations. The limiting retention factors of cations (i.e. the retention factor of the fully ion-paired analyte at very high additive concentration) are roughly proportional to their inherent hydrophobicities (i.e. the retention factor of the analyte in the absence of the anionic additive). With a given anion, differences in ion pairing strength between the solutes are required for effective selectivity adjustment. Based on the Wade–Lucy–Carr (W–L–C) kinetic model of overload peaks, the approach we developed in our previous work was used to study the effect of mobile phase anionic additives type and concentration on the limiting plate count (N₀) and sample loading capacity (ω_0.5) of various cationic drugs. Under linear chromatographic conditions, where the analyte exhibits its smallest peak width and thus maximum apparent plate count, the type and concentration of anionic additives have almost no effect on peak width. In comparison to neutral analytes the sorption isotherms of cationic species are very easily overloaded even when many fewer moles of cations as compared to neutrals are injected. We showed that different anionic additives profoundly affect the cations’ “overload profiles” (i.e. plots of plate count versus amount injected) by changing the sample loading capacities. The increase in sample loading capacities with different anions show the same order as the extent of ion pairing between the anions and the basic analytes. The detrimental effect of sample overloading on peak width can be greatly diminished by using either a stronger ion pairing agent or a higher concentration of a given ion pairing agent. Both effects operate by increasing the sample loading capacity, thereby allowing more solute to be injected. We believe that the increase in sample loading capacity described above is due in part to the increase in the number of ion-exchange sites as more anions sorb to the stationary phase. At the same time, the formation of a neutral ion-paired analyte also increases the amount of cation which can be loaded onto the stationary phase by allowing a greater fraction of the analyte to be present in the stationary phase as an electrically neutral (i.e. ion-paired) species.     

Online process control of acidic texturisation baths with ion chromatography

Etching of silicon with mixtures of hydrofluoric acid and nitric acid is a widely used process in silicon solar cell fabrication. One precondition for an optimized usage of the acidic etching baths is the exact knowledge of the chemical bath composition. In this paper, we investigated a fast and online-capable method for the total analysis of all bath constituents by ion chromatography. The chromatographical system consists of a low-volume injection valve, which injects the concentrated samples directly into the KOH-based eluent. After separation and detection of nitrate and fluoride, a post-column derivatization with sodium molybdate is applied to detect the hexafluorosilicic acid, which enriches in the texturisation bath during the etching process. The results of the presented approach are discussed and compared with already published chromatographical and titration methods found in literature.     

马尔可夫过程H-值可加泛函的向前向后鞅分解

本文研究了马尔可夫H-值可加泛函的向前向后鞅分解.利用Lyons-Meyer-Zheng鞅分解得到了泛函数极限定理所必需的极大不等式和紧性结果,在最小条件限度内得到了马尔可夫过程经验测度的泛函中心极限定理,将该定理从实值情形推广到了希尔伯特值情形.     

Availability of inspected systems subject to shocks – A matrix algorithmic approach

We examine the limiting average availability of a maintained system that deteriorates due to random shock process and as a response to its usage (wear out). System’s failures are not self-announcing, hence, failures must be detected via inspection. We consider randomly occurring shocks that arrive according to a Poisson process and cumulatively damage the system. Two models are considered: in Model 1 the shock and wear out processes are independent of the external environment and in Model 2, the shocks arrival rate, the shock magnitudes and the wear out rate are governed by a random environment which evolves as a Markov process. We obtain the system’s availability for both models.     

Revisiting the shelf life constrained multi-product manufacturing problem

A multi-product manufacturing problem generally consists of the total cost minimization. In case where the shelf life constraint is imposed, various options to deal with the situation are widely discussed in the literature. These options include a reduction in the production rate and cycle time separately, and the simultaneous reduction of production rate and cycle time. When the production rate is decreased, the unit manufacturing cost increases and because of this the inventory holding costs need modification. In the existing literature, this has been ignored in the computation of cost and therefore a revisit to the problem has been justified. The present paper modifies the holding cost and this problem has been reformulated for the basic case. This has also been extended for an inclusion of shortages that are backordered completely or partially.     

条件Erlang分布双参数加法定理的推广

X(m)和Y(k)服从参数(m,λ)和(k,μ)的Erlang分布且相互独立.证明了在X(m)相似文献   

存在不精确数据情况下的环境效率分析

针对环境效率评价问题中存在不精确数据的一类典型问题进行了深入的分析,在回顾现有的不精确数据处理方法以及环境效率评价方法的基础上,基于加性DEA模型,提出一种新的环境效率评价方法.该方法不仅能够求解各个投入/产出数据的最佳精确值,而且能够进一步分析各个决策单元的无效性.通过算例分析对模型及方法的优越性进行了说明,提出的方法克服了现有不精确数据处理方法的局限性,能够有效地处理环境效率分析问题中的不精确数据,得到更为准确的环境管理信息,为环境管理提供更为有效的决策依据.     

Feynman-Kac Formula for Left Continuous Additive Functionals and Extended Kato Class Measures

The perturbation of the generator of a Borel right process by a signed measure is investigated, using probabilistic and analytic potential theoretical methods. We establish a Feynman-Kac formula associated with measures charging no polar set and belonging to an extended Kato class. A main tool of this approach is the validity of a Khas’minskii Lemma for Stieltjes exponentials of positive left continuous additive functionals.