夹层板方程的变换和四边简支矩形夹层板的变形问题

本文从杜庆华各向同性线性理论出发,经过变换把基本方程简化为相当于一个单层薄板的方程和三个弹性地基上的薄膜方程.指出了杜庆华各向同性线性理论与Hoff和Reissner理论之间的主要差别为相差一个或两个弹性地基上的薄膜方程.导出了均布载荷和集中载荷作用下四边简支板挠度的近似公式,并按几种理论进行了分析比较.此外,提出了1948年Reissner型线性理论有关挠度的边界条件.在夹层板的合成内力的计算中,发现弯矩与单层板的弯短相同.

黄土高原水蚀风蚀交错带不同土地利用类型土壤呼吸季节变化及其环境驱动

water wind erosion crisscross region; soil respiration rate; seasonal changes; land use pattern; soil temperature; soil moisture; 【摘要】 以黄土高原水蚀风蚀交错区神木县六道沟小流域为研究区,采用动态密闭气室法对植物生长季节(2007年5～10月)5种土地利用方式的土壤呼吸速率进行了测定,并结合水热因子,对不同土地利用方式间土壤呼吸速率的差异性以及其和温度、含水量之间的关系进行了分析。结果表明:5种土地利用类型土壤呼吸速率季节性变化均呈现单峰型曲线,与气温变化趋势一致,其7、8月份土壤呼吸速率均显著高于其它月份(P<0.05);生长季节土壤CO2平均释放速率顺序为:长芒草地>苜蓿地>柠条地>农地>沙柳地,草地在生长前期和旺盛期土壤呼吸强度均显著高于农地和灌木林地;除沙柳地和苜蓿地以外,在土壤呼吸与所有温度指标的关系中,与10cm深度的土壤温度相关性最好,且除沙柳地外,其它4种土地利用类型均与之达到显著相关;农地土壤呼吸对温度的响应最敏感(Q10值为2.20),除沙柳地(Q10值为1.48)外,其它4种土地利用类型Q10值均在2.0左右,接近于全球Q10的平均水平;通过Van’t Hoff模型估算,2007年植物整个生长季节(5～10月份),5种土地利用类型土壤呼吸量从高到低依次为:苜蓿地259gC·m-2,长芒草地236gC·m-2,柠条地226...

高压差热分析方法（HP-DTA）研究钙蒙脱石-氯化钙-水体系中的脱水作用

在开放（P_水Hoff线方程：0%: 1np= 15.008 - 7.237 * (1000/T) (0.5M) 0.9%: 1np=14.634-6.781* (1000/T) (1M) 1.8%: 1np = 15.347-7.130 * (1000/T) (2.82M) 5%: 1np = 14.717 - 6.381 * (1000/T) (5.63M) 10%: 1np = 14.270-5.806 * (1000/T) (11.26M) 20%: 1np = 14.580 - 5.831 * (1000/T) (16.9M) 30%: 1np = 14.412 - 5.519 * (1000/T)根据这些等式求出了在不同压力、温度下各种浓度的CaCl_2-H_2O流体的水逸度系数（￡）。由于至目前为止在文献中还没有这方面的实验研究报道，因而无法评价这一新方法所获得的数据的准确性。利用求得的￡值，在本篇论文中建立起了不同浓度的CaCl_2-H_2O流体影响钙蒙脱石脱水温度的热力学模式：TD' = [T_1*T_D*(ΔH_(tw) + ΔH_(sv)~盐）/[T_1*(ΔG + ΔH_(dn)~水）-T_D~* (ΔH_(av)~水-ΔH_(sv)~盐）在0-1M浓度范围内，可以认为ΔH_(dh)~水≈H_(dh)~盐，等式变为：TD' = (TD*ΔH_(dh))/(ΔG + ΔH_(dh)）根据这个模式，能推导出在实验浓度范围内，钙蒙脱石在盐水体系中的脱水温度。通过本次论文的实验研究知道在一般沉积盆地的埋芷条件下，钙蒙脱石矿物不会发生简单的脱水作用。在缺乏K~+和低盐度的环境中，含水相蒙脱石可稳定地存在在一定深度的地壳中因而不可忽略蒙脱石在海洋化学和俯冲带水来源中的作用。在选择处理簇射性废料的回填料（backfill）时，如其它条件相同，则应优先选择钙蒙脱石，而不是蛭石。在石油采矿和勘探工程中，因压力释放所造成的蒙脱石的脱水作用可能是使钻井变大和塌方的可能性原因之一。

Chiral separation of enantiomers of amino acid derivatives by high-performance liquid chromatography on a norvancomycin-bonded chiral stationary phase

A novel norvancomycin-bonded chiral stationary phase (NVC-CSP) was synthesized by using the chiral selector of norvancomycin. The chiral separation of enantiomers of several dansyl-amino acids by high-performance liquid chromatography (HPLC) in the reversed-phase mode is described. The effects of some parameters, such as organic modifier concentration, column temperature, pH and flow rate of the mobile phase, on the retention and enantioselectivity were investigated. The study showed that ionic, as well as hydrophobic interactions were engaged between the analyte and macrocycle in this chromatographic system. Increasing pH of buffers usually improved the chiral resolution for dansyl-alpha-amino-n-butyric acid (Dns-But), dansyl-methionine (Dns-Met) and dansyl-threonine (Dns-Thr), but not for dansyl-glutamic acid (Dns-Glu) which contains two carboxylic groups in its molecular structure. The natural logarithms of selectivity factors (In alpha) of all the investigated compounds depended linearly on the reciprocal of temperature (1/T), most processes of enantioseparation were controlled enthalpically. Interestingly, the process of enantioseparation for dansyl-threonine was enthalpy-controlled at pH of 3.5, while at pH of 7.0, it was entropy-controlled according to thermodynamic parameters Delta(R,S)DeltaHdegrees and Delta(R,S)DeltaSdegrees afforded by Van't Hoff plots. In order to get baseline separation for all the solutes researched, norvancomycin was also used as a chiral mobile phase additive. In combination with the NVC-CSP remarkable increases in enanselectivity were observed for all the compounds, as the result of a "synergistic" effect. (C) 2003 Elsevier B.V. All rights reserved.