聚羟基铝柱撑蒙脱石吸附重金属离子实验研究

利用keggin离子对蒙脱石进行柱撑制得聚羟基铝柱撑蒙脱石,研究柱撑蒙脱石对Cu^2＋,Cd^2＋,Cr^3＋3种重金属离子的吸附。结果表明：未经焙烧的柱撑蒙脱石对Cu^2＋,Cr^3＋离子的吸附性要比原矿好,而经400℃下焙烧的柱撑蒙脱石对Cd^2＋则有更好的吸附性。用腐殖酸对柱撑蒙脱石改性能提高柱撑蒙脱石对3种重金属离子的吸附性能,柱撑蒙脱石对3种重金属离子的吸附量都随pH值的升高而增加。另外还对柱撑蒙脱石对3种重金属离子的吸附动力学进行了研究．发现其动力学吸附过程可用Elovicb方程和一级动力学方程进行较好的拟合。     

花岗岩酸岩作用反应动力学研究

化学刺激能够改善增强型地热系统(EGS)热储层裂隙连通情况、提高裂隙渗透率。本文以EGS热储化学刺激为出发点,开展土酸体系-花岗岩作用实验,总结实验规律,明确了酸岩作用机理,建立多矿物耦合反应动力学模型并获取重要参数。得出以下结论:土酸中HF浓度越高,对花岗岩的溶蚀率和溶蚀速率就越大,但更易产生二次沉淀;酸液中离子的浓度与不同矿物溶蚀存在对应关系,Na⁺和K⁺分别来自于钠长石和伊利石,Al³⁺和硅来自长石类和黏土类矿物,Ca²⁺前期来自方解石,后期受钙长石和氟石影响;土酸-花岗岩反应为双重机制控制下的动力学反应;HF机制下的矿物溶解反应速率常数数量级约为10^-4～10^-5,比中性机制下的矿物的溶解速率提高了约9个数量级。研究结果可以为EGS储层化学刺激工作提供理论支持。     

Hydrogeology of desert springs in the Panamint Range,California, USA: Geologic controls on the geochemical kinetics,flowpaths, and mean residence times of springs

Over 180 springs emerge in the Panamint Range near Death Valley National Park, CA, yet, these springs have received very little hydrogeological attention despite their cultural, historical, and ecological importance. Here, we address the following questions: (1) which rock units support groundwater flow to springs in the Panamint Range, (2) what are the geochemical kinetics of these aquifers, and (3) and what are the residence times of these springs? All springs are at least partly supported by recharge in and flow through dolomitic units, namely, the Noonday Dolomite, Kingston Peak Formation, and Johnnie Formation. Thus, the geochemical composition of springs can largely be explained by dedolomitization: the dissolution of dolomite and gypsum with concurrent precipitation of calcite. However, interactions with hydrothermal deposits have likely influenced the geochemical composition of Thorndike Spring, Uppermost Spring, Hanaupah Canyon springs, and Trail Canyon springs. Faults are important controls on spring emergence. Seventeen of twenty-one sampled springs emerge at faults (13 emerge at low-angle detachment faults). On the eastern side of the Panamint Range, springs emerge where low-angle faults intersect nearly vertical Late Proterozoic, Cambrian, and Ordovician sedimentary units. These geologic units are not present on the western side of the Panamint Range. Instead, springs on the west side emerge where low-angle faults intersect Cenozoic breccias and fanglomerates. Mean residence times of springs range from 33 (±30) to 1,829 (±613) years. A total of 11 springs have relatively short mean residence times less than 500 years, whereas seven springs have mean residence times greater than 1,000 years. We infer that the Panamint Range springs are extremely vulnerable to climate change due to their dependence on local recharge, disconnection from regional groundwater flow (Death Valley Regional Flow System - DVRFS), and relatively short mean residence times as compared with springs that are supported by the DVRFS (e.g., springs in Ash Meadows National Wildlife Refuge). In fact, four springs were not flowing during this campaign, yet they were flowing in the 1990s and 2000s.     

Comparative Studies on Phosphorus Uptake and Growth Kinetics of the Microalga Tetraselmis subcordiformis and the Macroalga Ulva pertusa

Short-term uptake experiments and long-term semicontinuous culture experiments were performed under the condition of phosphorus (P) limitation to estimate and compare the P uptake and growth kinetics of the microalga Tetraselmis subcordiformis and the macroalga Ulva pertusa. Two new parameters, the maximum specific uptake rate (Vm^sp) and the maximal growth efficiency (β), are introduced to achieve uniformity for the comparison of nutrient uptake and growth efficiency between microalgae and macroalgae. T. subcordiformis possesses 3 times lower half saturation uptake constant, 4 times higher maximal growth rate and 20 times higher maximum specific uptake rate than U. pertusa, while U. pertusa possesses 4 times higher maximal growth efficiency than T. subcordiformis.     

STUDY ON KINETICS OF GLUCOSE UPTAKE BY SOME SPECIES OF PLANKTON

The. rates of glucose uptake by some species of plankton were determined by 3H-glucose tracer method. Experimental results indicated that the observed glucose uptake at natural sea water concentrations by Platymonas subcordiformis and Brachionus plicatilis was principally a metabolic process fitted with the Michaelis-Menten equation in the range of adaptive temperatures. Heterotrophic uptake by Platymonas subcordiformis was mainly dependent on diffusion at high glucose levels. The uptake by Brachionus plicatilis showed active transport even at high glucose levels, indicating its high heterotrophic activity. The uptake rate by Anemia salina was lower, and its Vm/K ratio was lower than those of the other two species of plankton.     

稠油注蒸汽热采过程中的水化学问题

本文简要论述了稠油注蒸汽采过程中所引发出的水化学问题,指出:在注蒸汽热采过程中,随着蒸汽的注入,将在储层内自注热井向四周逐渐形成一些连续过渡的温、压、pH值和水相状态不同的汽水浸润带,即蒸汽饱和带→蒸汽过热水混合带→过热水带→与储层温压条件相当的热水带,由于各带内状态条件的不同,故各带内所引发出的水-岩作用(包括矿物的溶解与沉淀作用)将是有所不同的,因而对各带内储层孔隙结构的影响程度也将是不同的。文中还扼要地介绍了对此进行水化学研究的方法原理和研究途径。     

Relative-rate study of the gas-phase reaction of hydroxy radicals with difunctional organic nitrates at 298 K and atmospheric pressure

Rate coefficients for the reactions of difunctional nitrates with atmospherically important OH radicals are not currently available in the literature. This study represents the first determination of rate coefficients for a number of C(3) and C(4) carbonyl nitrates and dinitrates with OH radicals in a 38 l glass reaction chamber at 1000 mbar total pressure of synthetic air by 298±2 K using a relative kinetic technique.The following rate coefficients (in units of 10^-12 cm³ molecule^-1 s^-1) were obtained: 1,2-propandiol dinitrate, <0.31; 1,2-butandiol dinitrate, 1.70±0.32; 2,3-butandiol dinitrate, 1.07±0.26; -nitrooxyacetone, <0.43; 1-nitrooxy-2-butanone, 0.91±0.16; 3-nitrooxy-2-butanone, 1.27±0.14; 1,4-dinitrooxy-2-butene, 15.10±1.45; 3,4-dinitrooxy-1-butene, 10.10±0.50.The possible importance of reaction of OH as an atmospheric sink for the compounds compared to other loss processes is considered.     

Peroxy Radical Kinetics Resulting from the OH-Initiated Oxidation of 1,3-Butadiene, 2,3-Dimethyl-1,3-Butadiene and Isoprene

The laser flash photolysis/UV absorption spectrometry technique has been used to investigate the kinetics of the peroxy radical permutation reactions (i.e. self and cross reactions) arising from the OH-initiated oxidation of isoprene (2-methyl-1,3-butadiene), and of the simpler, but related conjugated dienes, 1,3-butadiene and 2,3-dimethyl-1,3-butadiene. The results of the two simpler systems are analysed to provide values of the rate coefficients for the 6 peroxy radical permutation reactions of the three types of isomeric peroxy radical produced in each system (T = 298 K, P = 760 Torr). The rate coefficients are all significantly larger than values estimated previously by extrapolation of structure-reactivity relationships based on the kinetics of a limited dataset of simpler radicals containing similar structural features. The results are discussed in terms of trends in self and cross reaction reactivity of primary, secondary and tertiary peroxy radicals containing combinations of allyl, -hydroxy and -hydroxy functionalities. Since the peroxy radicals formed in these systems are structurally very similar to those formed in the isoprene system, the kinetic parameters derived from the results of the simpler systems are used to assist the assignment of kinetic parameters to the 21 permutation reactions of the six types of isomeric peroxy radical generated in the isoprene system. Kinetic models describing the OH-initiated degradation of all three conjugated dienes to first generation products in the absence of NO_x are recommended, which are also consistent with available end product studies. The model for isoprene is considered to be a further improvement on that suggested previously for its OH-initiated oxidation in the absence of NO_x. The mechanism is further extended to include chemistry applicable to NO_x-present conditions, and calculated product yields are compared with those reported in the literature.     

The Rate-equation for Biogenic Silica Dissolution in Seawater – New Hypotheses

This paper investigates the kinetics of biogenic silica dissolution in seawater, through batch dissolution, where the reaction is observed as the increase in dissolved silicic acid concentration with time. It utilises new data from dissolution of the marine diatom Cyclotella cryptica, and the freshwater diatom C. meneghiniana, as well as literature results. The sum of exponentials form: , is hypothesised as the most general rate equation, with the single exponential form occurring in a minority of cases. The consistency of this behaviour with a near-exponential decay of surface area with time, an appropriate mathematical integration, and surface heterogeneity, is discussed. (Serious errors in some existing integrations are identified.) The rate of dissolution at constant surface area is shown to decrease non-linearly as the ambient concentration of silicic acid increases. A fractional order with respect to silicic acid in the back reaction, close to 0.5, leads to a mechanism in which an intermediate is formed from the surface and an, as yet, unidentified molecule, probably water. Good preliminary fits are found between the model and literature results found using entirely different methods. A parallel treatment of hydrogen ion dependency is suggested. The likely distortion of full reaction curves from exponential behaviour imposed by the back reaction, is considered in detail.     

Molecular iodine reduction by natural and model organic substances in seawater

The reactivity of 2 µM molecular iodine in seawater toward various organic compounds containing aromatic, -keto, amino, olefinic and sugar functional groups was investigated. More detailed studies have been made of the reduction kinetics with salicylic acid, -ketoglutaric acid and the polypeptide oxidized glutathione, particularly to establish whether variation over the pH range 4–9 would provide a similar reduction reactivity or fingerprint to that of molecular iodine added to natural seawater. The data indicates that compounds with only one functional group react with first order kinetics whereas compounds with multiple functional groups show more complex behaviour. Kinetic and thermodynamic modelling indicates that HOI is the main iodine species reacting with organic matter at seawater pH of 8.2. Based on the pH fingerprints, peptides and compounds containing carbonyl or -keto groups are the key reductants of molecular iodine added to seawater. These compounds form C-I and N-I bonds which can allow for a rich organic iodine chemistry in seawater. The model compound results are discussed in relation to oceanic processes.