一类时变需求且存货影响销售率的EOQ模型

从实际背景出发,在R AM P型需求和存货影响销售率条件下,讨论了一类以缺货开始的变质性物品的EOQ模型.给出了模型的求解方案及单位时间内平均利润最大化的两个充分条件,并用数值算例进行了验证.     

光盘阵列系统的一种性能优化方法

提出了一种用低性能驱动器组建高性能光盘阵列系统性能的优化方法。针对传统的低性能光盘驱动器(驱动器内部数据传输率及接口速率均较低),提出了一种新型的数据传输模式。采用此优化方法可以使光盘阵列系统的整体性能得到较大地提高。同时还可以提高系统整体的性价比。     

Kinetic limit of a conservative lattice gas dynamics showing long-range correlations

An anisotropic lattice gas dynamics is investigated for which particles on ^d jump to empty nearest neighbor sites with (fast) rate ^–2 in a specified direction and some particular configuration-dependent rates in the other directions. The model is translation and reflection invariant and is particle conserving. The space coordinate in the fast-rate direction is rescaled by ^–1. It follows that the density field converges in probability, as 0, to the corresponding solution of a nonlinear diffusion-type equation. The microscopic fluctuations about the deterministic macroscopic evolution are determined explicitly and it is found that the stationary fluctuations decay via a power law (1/r ^d ) with the direction dependence of a quadrupole field.     

Relationships between characteristics in periodic Poisson queues

We study single server periodic queues in the day equilibrium conditions. The following characteristics of interest are considered at time of dayt: V^p(t)-the work load, L^p(t)-the number of customers and u^p(t)-the departure rate. We give relationships between E[V^p(t)], E[L^p(t)] and u^p(t). We also prove that E[V^p(t)] < and E[L^p(t)] < provided the second moment of the service time is finite.     

Slow quenching for a one-dimensional kinetic Ising model: Residual energy and domain growth

A one-dimensional kinetic Ising model with Glauber dynamics subjected to a slow continuous quench to zero temperature is studied. For a rather general class of cooling schemes, described by a time-dependent temperatureT(t), the mean domain sizeL(t) is calculated along with the residual energye _res (r) as a function of the cooling rater. If the attempt frequency =₀ exp(–/kT), entering into the transition rates, is temperature dependent (i.e., the barrier is non-zero), the asymptotic growth ofL(t) is given byL()–L(t)~exp[–/kT(t)]. For this case the residual energy exhibits a power-law behaviore _res(r) ~r ^{/2(1 + )} forr small, where =4J/ andJ is the nearest neighbor coupling constant. For =0 and for certain cooling schemes the residual energy is zero andL(t)~t1/2, independent ofr.     

粒径和流速对吸附速率的影响

本文主要考察了吸附剂的粒径大小及动态循环时流速大小对吸附速率的影响，根据膜扩散限制和孔隙扩散限制的理论模型对其影响作了定量描述。     

中国的百岁老人研究Ⅱ.百岁老人的死亡率、生存率和发展趋势

根据全国人口普查资料,用指数函数拟合法计算了中国百岁老人的死亡率和生存率,得出中国人口的最高自然寿限为120岁,并预测到2010年中国百岁老人绝对数将达4万多人,届时每百万人口中将有30位百岁老人,比2000年增加1倍以上。     

椭圆法用于阳极溶出伏安法测定微量银

用新物理量Ｖｏｐ的椭圆法对阳极溶出伏安法分析的含银离子浓度为１０＾５－１０＾－９ｍｏｌ／Ｌ的一系列溶液进行了研究。结果表明：光学方法与电化学方法所得分析结果相同；椭圆法可检测的浓度下限比电化学方法低一个数量级以上。而且测量的相对平均偏差也小于电化学方法。     

杂氮硅三环成环反应的研究

本文报导了与硅原子直接相连的有机基团(R)对杂氮硅三环成环速率的影响。利用气相色谱检测成环反应的产物之一——乙醇的生成速率和数量,并同与硅相连的R基团对成环反应速率的影响作比较。实验结果表明五种杂氮硅三环成环速度顺序为Cl_2CH—>ClCH_2—>ClCH_2CH_2CH_2—>CH_2=CH—>CH_3—,这与理论推断相符。     

Solid-state interactions and drug release of teicoplanin in binary combinations with peracetylated α-, β-, and γ-cyclodextrins

Triacetyl α-cyclodextrin, triacetyl β-cyclodextrin and triacetyl γ-cyclodextrin were tested as possible hydrophobic carriers to prolong the release of hydrophilic teicoplanin (TCP). Physical–chemical characterization of individual components, drug-carrier physical mixtures at 0.5, 0.67 and 0.75 mass fraction of carrier, and the respective interaction products by kneading or evaporative crystallization under microwave irradiation was carried out using differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). In vitro drug release in pH 7.4 phosphate buffer at 37 °C was determined by intrinsic dissolution rate (IDR) measurements on non disintegrating compressed discs. Solid-state interactions of TCP with triacetyl α-cyclodextrin by evaporative crystallization and kneading and with triacetyl β-cyclodextrin by evaporative crystallization (probably resulting in carrier amorphization) were demonstrated. The role of carrier hydrophobicity, carrier mass fraction and preparation method of solid drug-carrier combinations on solid-state drug-carrier interactions and slowing down of TCP release was assessed. Modulation of drug release can be achieved using TCP-triacetyl γ-cyclodextrin combinations at 0.5 mass fraction of carrier.