用水化学动力学方法分析评价苏锡常地区孔隙Ⅱ承压水超采状态下补给条件的意义

基于孔隙承压水属性,研究了苏锡常地区孔隙Ⅱ承压水超采状态下最大水位埋深期（1994年、1998年）地下水动态（水位、水质）监测资料与水文地质条件。论述水位动态虽能直观反映开采状态下水资源衰竭与水位变化特征,但对补给条件及水动力机制不清楚,则会给超采状态下水文地质条件认识及评价带来视觉上的偏颇。采用水化学动力参数则能很好地反映不同水源补给空间的变化规律,用其常量水化学组分（K+、Na+、Ca2+、Mg2+、Cl-、HCO-3、CO2-3、SO2-4）计算的离子强度（I）、主要离子活度（aHCO-3、aNa+     

无机盐类对干酪根生烃过程的影响

利用岩石热解评价仪（Rock-Eval）和热解气相色谱仪（Py-GC)，对采自东营凹陷和松辽盆地的烃源岩干酪根进行了热模拟实验，探讨了地层水中所存在的无机盐类对生烃过程的影响，求得了不同盐类作用下的反应动力学参数。结果表明，无机盐类对干酪根的热解生烃过程具有不同的影响。其中，氯化盐类具有一定程度的反催化作用，其他盐类表现出正的催化作用。这种催化作用是通过降低热解反应的表观活化能或提高反应的频率因子而表现出来的。最后，对无机盐类的催化作用机制进行了初步探讨，认为电子诱导效应理论可以初步解释无机盐类的催化作用。     

论南方海相层系有效供烃能力的主要控制因素

通过对烃源条件和天然气成藏过程的动力学分析,从高有机质丰度海相碎屑岩层段发育、构造沉积类型特征、高—过成熟阶段烃源灶性质演变形成的气源接替效应以及生烃强度与非构造性散失强度(速率)在地质历史中数量关系等若干方面,探讨了影响中国南方海相层系天然气成藏的有效供烃能力的主要地质-地球化学因素。指出有效供烃效率是烃源岩性质、构造-沉积类型、烃源灶类型及其叠合、生烃强度历史演化和天然气散失速率诸控制要素的综合效应。提出烃源条件分级评价指标,并对南方海相层系的有效供烃能力进行了初步评价。     

电解脱氮除磷技术在海产养殖废水治理中的研究

海产养殖迅速发展造成水域富营养化、赤潮频发,海产养殖废水污染的治理迫在眉睫。为解决此问题将电解脱氮除磷技术应用在海产养殖废水处理中,并探讨电压、pH、极板间距和电解时间对脱氮除磷去除率的影响。结果表明:脱氮除磷的去除率与电压成正相关,与极板间距成负相关。在电压为30V,极板间距10cm,pH为7时,NH_4~+-N、NO_3~--N和TP的去除率达到最大分别为72%、90%、85%。     

高温胁迫对三角褐指藻和纤细角毛藻叶绿素荧光动力学的影响

研究高温胁迫(35~50℃)对三角褐指藻和纤细角毛藻叶绿素荧光动力学的影响。利用调制式叶绿素荧光仪(Wa-ter-PAM)测定了:PSⅡ的最大光能转化效率(Fv/Fm);PSⅡ的潜在活性(Fv/Fo);PSⅡ的实际光能转化效率(ΦPSⅡ=yield);光合电子传递效率(ETR);光化学淬灭(qP)和非光化学淬灭(NPQ)等主要参数。结果表明,与对照组相比,高温胁迫下2种硅藻的叶绿素荧光参数Fv/Fm,Fv/Fo,ΦPSⅡ,ETR和qP均明显降低,并且随着胁迫温度的升高,胁迫时间的延长,下降幅度也逐步增大;NPQ则先升高后下降。另外,还对高温胁迫下2种硅藻的响应机制以及叶绿素荧光技术在筛选耐高温微藻品系中的应用进行了初步探讨。     

同步卫星短弧定轨

同步卫星受到摄动力的影响,它的实际轨道有一点漂移．卫星需要不断的调轨调姿,以保证其正常运行．为了研究卫星在几小时,甚至更短的时间内的轨迹情况,采用短弧段定轨法．用动力学方法进行短弧定轨,分别研究1小时和15分钟定轨并进行比较,目的是为了在同步轨道卫星变轨后,能尽快地为卫星提供精密的预报轨道．此外,在系列短弧定轨后,得到精密轨道系列,为研究轨道变化的力学因素及研究短弧中卫星转发器时延变化规律等提供依据．     

A Study of the Migration and Accumulation Efficiency and the Genesis of Hydrocarbon Natural Gas in the Xujiaweizi Fault Depression

In order to investigate the migration and accumulation efficiency of hydrocarbon natural gas in the Xujiaweizi fault depression, and to provide new evidence for the classification of its genesis, a source rock pyrolysis experiment in a closed system was designed and carried out. Based on this, kinetic models for describing gas generation from organic matter and carbon isotope fractionation during this process were established, calibrated and then extrapolated to geologic conditions by combining the thermal history data of the Xushen-1 Well. The results indicate that the coal measures in the Xujiaweizi fault depression are typical ＂high-efficiency gas sources＂, the natural gas generated from them has a high migration and accumulation efficiency, and consequently a large-scale natural gas accumulation occurred in the area. The highly/over matured coal measures in the Xujiaweizi fault depression generate coaliferous gas with a high δ^13C1 value （〉 -20‰） at the late stage, making the carbon isotope composition of organic alkane gases abnormally heavy. In addition, the mixing and dissipation through the caprock of natural gas can result in the negative carbon isotope sequence （δ^13C1 〉δ^13C2 〉δ^13C3 〉δ^13C4） of organic alkane gases, and the dissipation can also lead to the abnormally heavy carbon isotope composition of organic alkane gases. As for the discovery of inorganic nonhydrocarbon gas reservoirs, it can only serve as an accessorial evidence rather than a direct evidence that the hydrocarbon gas is inorganic. As a result, it needs stronger evidence to classify the hydrocarbon natural gas in the Xujiaweizi fault depression as inorganic gas.     

Calcite Dissolution in Deionized Water from 50℃ to 250℃ at 10 MPa： Rate Equation and Reaction Order

Carbonate minerals and water (or geofluids) reactions are important for modeling of geochemical processes and have received considerable attention over the past decades.The calcite dissolution rates from 50℃to 250℃at 10 MPa in deionized water with a flow rate varying from 0.2 to 5 mL/min were experimentally measured in a continuous flow column pressure vessel reactor.The dissolution began near the equilibrium with c/c_(eq)>0.3 and finally reached the equilibrium at 100℃-250℃,so the corresponding solubility was also determined as 1.87,2.02,2.02 and 1.88×10~(-4)·mol/L at 100℃,150℃,200℃and 250℃respectively,which was first increasing and then switching to decreasing with temperature and the maximum value might occur between 150℃and 200℃.The experimental dissolution rate not only increased with temperature,but also had a rapid increase between 150℃and 200℃at a constant flow rate of 4 mL/min.The measured dissolution rates can be described using rate equations of R=k(1-c/c_(eq))n or R=kc~(-n).In these equations the reaction order n changed with temperature,which indicates that n was a variable rather than a constant,and the activation energy was 13.4 kJ/mol calculated with R=k(1-c/c_(eq))~n or 18.0 k J/mol with R=kc~(-n),which is a little lower than the surface controlled values.The varied reaction order and lower activation energy indicates that calcite dissolution in this study is a complex interplay of diffusion controlled and surface controlled processes.     

OPTIMIZATION IN ORGANIC SYNTHESIS.AN APPROACH TO OBTAINING KINETIC INFORMATION BY SEQUENTIAL RESPONSE SURFACE MODELLING.OUTLINE OF THE PRINCIPLES

A method is presented by which it is possible to estimate the initial rate of chemical reactions when theexperimental conditions are varied according to a response surface design.The method is intended as acomplementary method for analysing data obtained from experiments in synthetic chemistry when theobjective is to optimize the yield of the reaction.Data obtained by simulations have been used to develop the method.From the simulated reactions itis shown that sequential analysis of the chemical yield of the reaction makes it possible to estimate modelswhich describe how the parameters of the response surface of the yield vary over time.The derivativesof these time functions of the response surface parameters can be used to define a rate function whichdescribes how the variations in the experimental conditions influence the rate of the reaction.It is shown how such rate functions can be used to afford reasonable estimates of the initial rates ofthe reaction.The initial reaction rates thus estimated can be used to determine the kinetic order of thereactants and also to provide estimates of the activation energy of the reaction.A thorough discussion of how canonical analysis of the rate function may assist in the elucidation ofreaction mechanisms is given.