川东北飞仙关组鲕滩气藏天然气运聚效率   总被引：3，自引：1，他引：2  

李吉君  卢双舫  薛海涛  胡国艺  谢增业  徐庆霞 《地球科学》2008,33(4):565-571

设计进行了封闭体系下原油裂解成气的模拟实验, 建立并标定了原油裂解成气及其碳同位素分馏的化学动力学模型, 以罗家寨气田罗家7井为例分别进行了地质应用.生烃动力学研究发现, 飞仙关组古油藏具备“高效气源灶”的特点, 原油在中晚侏罗世172~151Ma约20Ma时期内裂解殆尽, 且原油裂解气的生成与其运聚成藏作用具有良好的时空匹配关系, 由此可促成飞仙关组气藏天然气的高效运聚.碳同位素分馏动力学研究证实甲烷成藏参与率达87%.利用生烃动力学与碳同位素分馏动力学结合的方法对天然气的运聚效率进行探讨是一个新的有效途径.   相似文献   

Combustion Kinetics of Athabasca Bitumen from 1D Combustion Tube Experiments     

Xiaomeng Yang  Ian D. Gates 《Natural Resources Research》2009,18(3):193-211

There are two basic requirements for heavy-oil recovery processes: first, mobilize the bitumen, and second, have a drive mechanism deliver the mobilized bitumen to a production wellbore. In situ combustion has the potential to be an important heavy-oil recovery method. Before design of in situ combustion recovery processes can start, it is necessary as a first step to understand the kinetics of various complex chemical reactions and determine kinetic constants associated with the reactions. Even with modern reservoir simulation capabilities, this is a significant challenge. In this research, an Athabasca bitumen combustion tube experiment, conducted by the ISC Research Group at the University of Calgary, was history matched by using a reservoir thermal simulator to determine a set of kinetic parameters as well as the transport parameters for the system. The main results of the history match was a match of air injection rate, bitumen and gas production volumes, average product gas compositions, temperature profiles along the tube through time, and pressure. Gridding sensitivities were examined to determine if the derived kinetic and transport parameters were dependent on gridblock size. The results revealed that the grid was refined enough to sufficiently capture thermal, mass transfer, and reaction length scales. After this single match was achieved, the same constants were used to successfully predict several other combustion tube experiments. The results suggest that the fuel (coke) for high-temperature oxidation (HTO) originates mainly from low-temperature oxidation (LTO) and not from thermal cracking. This implies that the major control on HTO is upstream oxygen transfer into the LTO region. If LTO does not occur, then a relatively small amount of coke is deposited in the matrix due to thermal cracking and this may be insufficient to start or sustain HTO.  相似文献   

Adsorption kinetics, isotherm, and thermodynamic studies of adsorption of pollutant from aqueous solutions onto humic acid   总被引：1，自引：0，他引：1  

YaJun Wang  HongLang Xiao  Fang Wang 《寒旱区科学》2009,1(4):0372-0379

In the present study,humic acid was used as an adsorbent for the investigation of the adsorption kinetics,isotherms,and thermo-dynamic parameters of hexavalent chromium from aqueous solution at varying pH,temperatures,and concentrations.Adsorption isotherms and equilibrium adsorption capacities were determined by the fittings of the experimental data to three well-known iso-therm models:Langmuir,Freundlich,and Redlich-Peterson.The results showed that the Langmuir and Redlich-Peterson models appear to fit the adsorption better than did the Freundlich adsorption model for the adsorption of chromium onto humic acid.The equilibrium constants were used to calculate thermodynamic parameters such as the change of free energy,enthalpy,and entropy.The derived adsorption constants (logaL) and their temperature dependencies from Langmuir isotherm have been used to calculate the corresponding thermodynamic quantities such as the free energy of adsorption,heat,and entropy of adsorption.The thermo-dynamic data indicate that Cr (VI) adsorption onto humic acid is entropically driven and characterized by physical adsorption.  相似文献   

Comments on “Two-dimensional concentration distribution for mixing-controlled bioreactive transport in steady-state” by O.A. Cirpka and A.J. Valocchi     

Haibing Shao  Florian Centler  Cecilia De Biase  Martin Thullner  Olaf Kolditz 《Advances in water resources》2009

In this comment we present a re-analysis of the analytical solution presented by Cirpka and Valocchi for steady-state concentrations of dissolved bioreactive compounds and bacterial biomass in porous media. We discuss the validity range of the analytical solution. In particular, the criterion used to determine the sustainability of biomass is revisited. This re-analysis shows that the ω$\omega$ criterion used by Cirpka and Valocchi is only a necessary but not a sufficient criterion to determine the bioreactive zones. As a consequence, the analytical solution does not provide the exact distribution of compounds throughout the domain, but can serve as upper or lower boundaries for species concentrations at a given location. These conclusions are supported by the simulation results obtained from an established reactive transport model.  相似文献   

Surface selection,adhesion, and retention behavior of marine bacteria on synthetic organic surfaces using self-assembled monolayers and atomic force microscopy     

Chuan Zhao  Thorsten Brinkhoff  Malte Burchardt  Meinhard Simon  Gunther Wittstock 《Ocean Dynamics》2009,59(2):305-315

Adhesion of two marine bacteria Shewanella sp. strain T1 and Pseudoalteromonas sp. strain T8, on differently terminated alkanethiolate self-assembled monolayers on gold was investigated. The selected model surfaces—terminated by CH₃, OH, NH₂, COOH, OH-terminated oligo(ethylene glycol), and methyl-terminated oligo(ethylene glycol)—are characterized by contact angle measurement using water, methylene iodide, 1-bromonaphthalene, and formamide. Surface free energies were calculated. Cell counting of the two bacterial strains on the model surfaces after different times revealed differences between the two strains by at least one order of magnitude. For the different surfaces, the bacteria showed comparably small selectivity. Atomic force microscopy images of adhered bacteria showed very different fingerprints on the different surfaces. Electronic supplementary material  Supplementary material is available in the online version of this article at and is accessible to authorized users.  相似文献   

Performance of A Combination Process of UV/H2O2/Micro‐Aeration for Oxidation of Dichloroacetic Acid in Drinking Water     

WenHai Chu  N. Y. Gao  Y. Deng 《洁净——土壤、空气、水》2009,37(3):233-238

The decomposition of dichloroacetic acid (DCAA) in water using a UV/H₂O₂/micro‐aeration process was investigated in this paper. DCAA cannot be removed by UV radiation, H₂O₂ oxidation or micro‐aeration alone, while UV/H₂O₂/micro‐aeration combination processes have proved effective and can degrade this compound completely. With initial concentrations of about 110 μg/L, more than 95.1% of DCAA can be removed in 180 min under UV intensity of 1048.7 μW/cm², H₂O₂ dosage of 30 mg/L and micro‐aeration flow rate of 2 L/min. However, more than 30 μg/L of DCAA was left after 180 min by UV/H₂O₂ combination process without micro‐aeration with the same UV intensity and H₂O₂ dosage. The effects of applied UV radiation intensity, H₂O₂ dose, initial DCAA concentration and pH on the degradation of DCAA have been examined in this study. Degradation mechanisms of DCAA with hydroxyl radical oxidation have been discussed. The removal rate of DCAA was sensitive to operational parameters. There was a linear relationship between rate constant k and UV intensity and initial H₂O₂ concentration, which indicated that a higher removal capacity can be achieved by improvement of both factors. A newly found nitrogenous disinfection by‐product (N‐DBP)‐DCAcAm, which has the potential to form DCAA, was easier to remove than DCAA by UV/H₂O₂ and UV/H₂O₂/micro‐aeration processes. Finally, a preliminary cost comparison revealed that the UV/H₂O₂/micro‐aeration process was more cost‐effective than the UV/H₂O₂ process in the removal of DCAA from drinking water.  相似文献   

Rice Husk Ash as a Low Cost Adsorbent for the Removal of Methylene Blue and Congo Red in Aqueous Phases     

Anirban K. Chowdhury  Anupam D. Sarkar  Amitava Bandyopadhyay 《洁净——土壤、空气、水》2009,37(7):581-591

Adsorption is of significant importance for effluent treatment, especially for the treatment of colored effluent generated from the dyeing and bleaching industries. Low cost adsorbents have gained attention over the decades as a means of achieving very high removal efficiencies to meet effluent discharge standards. The present article reports on batch investigations for color removal from aqueous solutions of Methylene Blue (MB) and Congo Red (CR) using Rice Husk Ash (RHA) as an alternative low cost adsorbent. The performance analysis was carried out as a function of various operating parameters, such as initial concentration of dye, adsorbent dose, contact time, shaker speed, interruption of shaking and ionic concentration. Performance studies revealed that a very high percentage removal of color was achievable for both dyes. The maximum percentage removal of MB was 99.939%, while 98.835% removal was observed for CR. These percentage removals were better than existing systems. Detailed data analysis indicated that adsorption of MB followed the Temkin isotherm, while CR followed the Freundlich isotherm. These isotherms were feasible within the framework of experimentation. Batch kinetic data, on the other hand, indicated that pseudo second order kinetics governed adsorption in both cases. Sensitivity analysis further indicated that the effects of initial dye concentration, shaker speed, pH and ionic strength had no noticeable effect on the percentage dye removal at equilibrium. Batch desorption studies revealed that 50% acetone solution was optimum for CR, while desorption of MB varied directly with acetone concentration.  相似文献   

A Study of the Thermodynamics and Kinetics of Copper Adsorption Using Chemically Modified Rice Husk     

Hasanur Jaman  Debarati Chakraborty  Papita Saha 《洁净——土壤、空气、水》2009,37(9):704-711

The use of rice husk as a low cost adsorbent for the removal of copper from wastewater has been explored in a laboratory scale experiment. The rice husk used for the study was treated with alkali to increase the sorption properties. The influence of metal ion concentration, weight of biosorbent, stirring rates, temperature and pH were also evaluated, and the results are fitted using adsorption isotherm models. From the experimental results it was observed that almost 90–98% of the copper could be removed using treated rice husk. The Langmuir adsorption isotherm, Freundlich isotherm and Tempkin isotherm models were used to describe the distribution of copper between the liquid and solid phases in batch studies, and it was observed that the Langmuir isotherm better represented the adsorption phenomenon. The experimental rate constant, activation energy, Gibbs free energy, enthalpy and entropy of the reaction were calculated in order to determine the mechanism of the sorption process.  相似文献   

Heating rate dependency of petroleum-forming reactions: implications for compositional kinetic predictions     

V. Dieckmann  B. Horsfield  H. J. Schenk 《Organic Geochemistry》2000,31(12)

The generation of bulk petroleum, liquid and gaseous hydrocarbons from the Duvernay Formation was simulated by heating immature kerogens in a closed system (MSSV pyrolysis) at four different heating rates (0.013, 0.1, 0.7 and 5.0 K/min). Using the established parallel reaction kinetic model, temperature and compositional predictions were tested to be suitable for geological conditions by comparing the laboratory results with natural changes in source bitumens and reservoir oil maturity sequences from the Duvernay Formation. In the case of bulk liquid and gaseous hydrocarbons, the above kinetic calculations can be considered valid because their maximum yields are independent of laboratory heating rates. In contrast, the contents of paraffins, aromatics and sulfur compounds show a pronounced heating rate dependence. Extrapolated to geological heating rates, the compositional predictions are consistent with the bulk composition of natural products in the Duvernay-petroleum system showing an increase of paraffinicity and hydrogen content. In contrast to that, the “hump” decreases with decreasing heating rate, a trend which is confirmed by the low amounts of unresolved compounds in natural high maturity products. Because of these heating-rate dependent compositional changes, geological predictions of natural molecular composition by the commonly used kinetic models are not suitable.  相似文献   

煤中有机质二次生烃迟滞性及其反应动力学机制   总被引：25，自引：1，他引：24       下载免费PDF全文

秦勇  张有生 《地球科学》2000,25(3):278-282

采用自然成熟度系列与其预热残渣系列样品相结合方式, 通过热解模拟方法, 对煤中有机质二次生烃迟滞性显现特征和化学反应动力学机制进行了探讨.结果表明: 二次生烃起始成熟度增高, 二次生烃峰位成熟度呈规律性后移, 二次生烃作用“死线”位于R_o=4.0 %左右; 二次生烃峰位成熟度与起始成熟度之差随起始成熟度的增高呈抛物线式演化, 二次生烃的绝对迟滞性和相对迟滞性均呈阶段性演化, 由此可对二次生烃迟滞深度进行预测; 二次生烃半峰宽随起始成熟度呈阶段性演化, 暗示二次生烃起始成熟度位于生油高峰附近的烃源岩, 其生烃量可能相对较大.同时, 原始样品平均活化能的演化经历了4个阶段, 它们与热解生烃量及二次生烃迟滞性的阶段性演化特征高度吻合, 揭示出二次生烃作用严格受控于反应动力学的地球化学机制.   相似文献