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21.
22.
CORROSION AND ADHERENCE AT SEA OIL-PLATFORM   总被引:1,自引:0,他引:1  
Measurements of the adhesive corrosion and protective potentials of 3 Bohai Sea oilplatforms under different cathodic protection showed corrosion still occurred on these platforms undertheir designed protective potentials. Preliminary conclusions from indoor experiments on the relation betweenadhesive corrosion and cathodic protection showed adhering organisms caused the corrosion onthese platforms.  相似文献   
23.
含有多重极点的有理真分式展开为部分分式,不需要计算低阶导数。列出被求函数的各阶导数的关系式,画出各阶导数作为节点的信号流图。该图无环路,既直观表现出各高阶导数的相互关系及影响的单向性,也使求节点增益的梅森公式特别简便。该方法将求高阶导数问题简化为代数运算,特别适合于编制成计算机程序  相似文献   
24.
马春玉 《天文学报》1996,37(1):28-34
本文通过数值求解带电粒子与Alfven波湍动相互作用的动力学方程,得到了相对论电子在射电喷流中被加速随时间演化的解.高能电子可以加速到Lorentz因子γy~106,且形成稳态的幂律谱,尽管其谱指数S≈l比观测值小,但粒子加速时间约为1012-1014秒,小于射电斑的寿命107年.粒子能谱指数几乎与Alfven波谱指数和能量损失函数无关.能量损失对加速上限有较大影响.  相似文献   
25.
We carry out numerical simulations of dissipationless major mergers of elliptical galaxies using initial galaxy models that consist of a dark matter haloes and a stellar bulge with properties consistent with the observed fundamental plane. By varying the density profile of the dark matter haloes [standard Navarro, Frenk & White (NFW) profile versus adiabatically contracted NFW profile], the global stellar to dark matter mass ratio and the orbit of the merging galaxies, we are able to assess the impact of each of these factors on the structure of the merger remnant. Our results indicate that the properties of the remnant bulge depend primarily on the angular momentum and energy of the orbit; for a cosmologically motivated orbit, the effective radius and velocity dispersion of the remnant bulge remain approximately on the fundamental plane. This indicates that the observed properties of elliptical galaxies are consistent with significant growth via late dissipationless mergers. We also find that the dark matter fraction within the effective radius of our remnants increases after the merger, consistent with the hypothesis that the tilt of the fundamental plane from the virial theorem is due to a varying dark matter fraction as a function of galaxy mass.  相似文献   
26.
勘查地球化学对异常评价的最大不确定性源于对地球化学景观特性的认识不够。我们应用构造相空间的方法分析了浙江儒岙幅(1:5万)水系沉积物测量的Ag含量数据,揭示了地球化学景观是具有低维吸引子(DZ≈2.9)的混饨系统。这一发现将对勘查地球化学中采样密度的选择、地球化学场模拟、异常评价等根本性问题产生重大影响。  相似文献   
27.
The Late Permian (Wuchiapingian) Alcotas Formation in the SE Iberian Ranges consists of one red alluvial succession where abundant soil profiles developed. Detailed petrographical and sedimentological studies in seven sections of the Alcotas Formation allow six different types of palaeosols, with distinctive characteristics and different palaeogeographical distribution, to be distinguished throughout the South‐eastern Iberian Basin. These characteristics are, in turn, related to topographic, climatic and tectonic controls. The vertical distribution of the palaeosols is used to differentiate the formation in three parts from bottom to top showing both drastic and gradual vertical upwards palaeoenvironmental changes in the sections. Reconstruction of palaeoenvironmental conditions based on palaeosols provides evidence for understanding the events that occurred during the Late Permian, some few millions of years before the well‐known Permian‐Triassic global crisis.  相似文献   
28.
羊蹄子山-磨石山钛矿床的钛矿物主要为锐钛矿、金红石和钛铁矿。锐钛矿化学成分的特点是FeO含量明显比金红石要低;主要X光粉晶谱线为3.518(100)、2.377(14)和1.667(11);晶胞参数a()=3.786,c()=9.513;拉曼光谱谱线(cm-1)为516、395、195和143。金红石的主要X光粉晶谱线为3.250(100)、1.688(40)和2.488(29);晶胞参数为a()=4.595,c()=2.962;拉曼光谱谱线(cm-1)为610和446。钛铁矿的成分特点是富锰贫镁,与攀西地区岩浆型钒钛磁铁矿矿床中的钛铁矿正好相反。所有上述钛(铁)氧化物矿物学特征,进一步说明该矿床是在中元古代在海底与基性火山活动有关的热水沉积后经区域变质和局部又遭受后期热液改造而成。  相似文献   
29.
Over a period of 4 years and 4 months, the geopurification installations at Dehesas de Guadix (Granada, Spain) were monitored to determine the impact on soil and groundwater of the controlled discharge of urban wastewater, and also to identify the best indicators of the entry of the recharged water into the aquifer. The installations are located in an area where the climate is Mediterranean sub-arid, with an average precipitation of less than 287 mm/year, and a rate of evapotranspiration that is almost three times greater. The system was controlled by determining the balance of majority nutrients and boron in the soil and in the groundwater, both at the points affected directly by the wastewater discharge and at others. The quantity of mass discharged was relatively large (COD 14,656 g/m2, NO3 85 g/m2, NO2 4 g/m2, NH4 2,425 g/m2, PO4 1,143 g/m2, K 1,531 g/m2, B 63 g/m2). It was observed that the elimination of nutrients within the soil (COD 97.5%, PO4 94.4%, K 59.17%, N total 18.8%, B 12.69%) was very efficient except for the nitrogen, which nevertheless did not reach the groundwater, as it was eliminated at deep levels of the unsaturated zone. Only 12.69% of the boron was removed, and appreciable, increasing amounts of this element did reach the groundwater. Unexpectedly, none of the majority nutrients behaved as a reliable indicator of the impact on groundwater; despite this, the boron and the bicarbonate did clearly reflect the arrival of the recharged water, and are proposed as the best indicators.  相似文献   
30.
Hydrogen sulfide (H2S) is known to catalyze thermochemical sulfate reduction (TSR) by hydrocarbons (HC), but the reaction mechanism remains unclear. To understand the mechanism of this catalytic reaction, a series of isothermal gold-tube hydrous pyrolysis experiments were conducted at 330 °C for 24 h under a constant confining pressure of 24.1 MPa. The reactants used were saturated HC (sulfur-free) and CaSO4 in the presence of variable H2S partial pressures at three different pH conditions. The experimental results showed that the in-situ pH of the aqueous solution (herein, in-situ pH refers to the calculated pH of aqueous solution under the experimental conditions) can significantly affect the rate of the TSR reaction. A substantial increase in the TSR reaction rate was recorded with a decrease in the in-situ pH value of the aqueous solution involved. A positive correlation between the rate of TSR and the initial partial pressure of H2S occurred under acidic conditions (at pH ∼3-3.5). However, sulfate reduction at pH ∼5.0 was undetectable even at high initial H2S concentrations. To investigate whether the reaction of H2S(aq) and occurs at pH ∼3, an additional series of isothermal hydrous pyrolysis experiments was conducted with CaSO4 and variable H2S partial pressures in the absence of HC at the same experimental temperature and pressure conditions. CaSO4 reduction was not measurable in the absence of paraffin even with high H2S pressure and acidic conditions. These experimental observations indicate that the formation of organosulfur intermediates from H2S reacting with hydrocarbons may play a significant role in sulfate reduction under our experimental conditions rather than the formation of elemental sulfur from H2S reacting with sulfate as has been suggested previously (Toland W. G. (1960) Oxidation of organic compounds with aqueous sulphate. J. Am. Chem. Soc.82, 1911-1916).Quantification of labile organosulfur compounds (LSC), such as thiols and sulfides, was performed on the products of the reaction of H2S and HC from a series of gold-tube non-isothermal hydrous pyrolysis experiments conducted at about pH 3 from 300 to 370 °C and a 0.1-°C/h heating rate. Incorporation of sulfur into HC resulted in an appreciable amount of thiol and sulfide formation. The rate of LSC formation positively correlated with the initial H2S pressure. Thus, we propose that the LSC produced from H2S reaction with HC are most likely the reactive intermediates for H2S initiation of sulfate reduction. We further propose a three-step reaction scheme of sulfate reduction by HC under reservoir conditions, and discuss the geological implications of our experimental findings with regard to the effect of formation water and oil chemistry, in particular LSC content.  相似文献   
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