Corrosion behavior of anodic oxidized TiO<Subscript>2</Subscript> film in seawater

TiO₂ films were formed on metallic titanium substrates by the anodic oxidation method in H₂SO₄ solution under the 80V D.C.. Phase component and microstructure were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Water contact angles on titanium oxide film surface were measured under both dark and sunlight illumination conditions. Corrosion tests were carried out in seawater under different illumination conditions by electrochemistry impedance spectrum (EIS) and polarization curves. The result showed that the TiO₂ film prepared by the anodic oxidation method was anatase with a uniform structure and without obvious pores or cracks on its surface. The average water contact angle of the film was 116.4° in dark, in contrast to an angle of 42.7° under the UV illumination for 2 hours, which demonstrates good hydrophobic property. The anti-corrosion behavior of the TiO₂ film was declining with the extended immersion time. Under dark conditions, however, the hydrophobic TiO₂ film retarded the water infiltrating into the substrate. The impedance changed slowly and the corrosion current density was 2 orders of magnitude lower than that with the film illuminated by sunlight. All of those mentioned above indicate that the TiO₂ film possesses much better performance under dark condition, and it can be applied as an engineering material under dark seawater environment.     

稠油成因研究综述

在阐述稠油地球化学特征基础上,对稠油的成因及其判识的最新研究进展进行了综述,稠油成因类型分原生型和次生型,其中,次生型稠油主要由生物降解、水洗和氧化作用分解、消耗或氧化原油中的烃类组分,使非烃和沥青质含量相对增加,致使原油密度和黏度增大,油质变稠.最后指出了目前稠油成因机制研究中存在的问题以及今后发展的方向.     

Oxidation state of lithospheric mantle along the northeastern margin of the North China Craton: implications for geodynamic processes

Quaternary volcanic rocks in the Kuandian (KD), Longgang (LG), Changbaishan (CBS), Wangqing (WQ), and Jilin (JL) volcanic centres in eastern Liaoning and southern Jilin provinces contain mantle xenoliths of spinel-facies lherzolites and minor harzburgites. Among the study sites, the KD, LG, and CBS volcanic fields are located on the northeastern margin of the North China Craton (NCC), whereas the WQ and JL fields lie on the southern margin of the Xing'an–Mongolia Orogenic Belt (XMOB). The (Fo) components of olivine (Ol) and Cr# (=Cr/(Cr + Al)) of spinel, together with trace element abundance of clinopyroxene, suggest that the subcontinental lithospheric mantle (SCLM) in the study area has undergone a low degree (4–6%) of partial melting. The rocks do not show modal metasomatism, but clinopyroxene grains in selected samples show elevated large ion lithophile element compositions, suggesting that the mantle xenoliths underwent minor cryptic metasomatism by exchange with a silicate melt. Two-pyroxene thermometry yielded equilibration temperatures ranging from 740°C to 1210°C. The corresponding oxygen fugacity (fO₂) was calculated to range from FMQ –2.64 to +0.39 with an average of –0.59 (n?=?53). The oxidation state is comparable to that of abyssal peridotites and the asthenospheric mantle. We failed to discover differences in equilibration temperatures and oxidation state between lherzolites and harzburgites, suggesting that partial melting did not affect fO₂ values. In addition, similar fO₂ of non-metasomatized and metasomatized samples suggest that metasomatism in the region did not affect fO₂. Our data suggest that the present SCLM beneath the northeastern margin of the NCC and the southern margin of the XMOB are very similar and likely formed from a fertile asthenosphere after delamination of an old lithospheric keel below the NCC in response to the west-dipping subduction of the Pacific oceanic plate since early to middle Mesozoic time.     

Weathering mechanisms and their effects on landsliding in pelitic schist

Physical, chemical, and mineralogical analyses of undisturbed drill cores of pelitic schist from a landslide area in Japan clarified the mechanisms of chemical weathering of pelitic schist. Oxidizing surface water percolates downward and reaches an oxidation front, where chlorite is altered to Al‐vermiculite, graphite and pyrite are oxidized and depleted, and goethite precipitates. Oxidation of pyrite also occurs just below the oxidation front, probably by ferric iron. Pyrite oxidation yields sulphuric acid, which penetrates further downward, interacting with and weakening the rocks. In addition to this chemical weakening, stress release and shearing along schistosities form an incipient shear zone, which propagates to a sliding zone that forms the rupture surface of a landslide. Once a sliding zone has developed, it inhibits downward groundwater flow across it because of its low permeability, slowing the downward propagation of the weathering zone until this filtration barrier is broken by landslide movement. Copyright © 2010 John Wiley & Sons, Ltd.     

九龙江河口沉积物中硫酸盐还原与甲烷厌氧氧化:同位素地球化学证据

通过沉积物柱孔隙水中甲烷,SO2-4,Cl-,δc(34S-SO2-4)、δc(13 C-CH4)的垂直分布特征,研究了硫酸盐还原和甲烷厌氧氧化(anaerobic oxidation of methane,简称AOM)过程在九龙江河口沉积物中的分布规律.测定结果显示两个站位(J-A和J-E)间隙水中SO2-4浓度随深...     

川西高原水环境的氧化还原特征初探

从川西高原饮用水赋存的环境-地质条件出发进行研究,较全面的探讨了该区气象、水文、土壤等环境要素对水中氧化还原电位的制约作用。通过对研究区内饮用水赋存环境的一系列环境地质调查与氧化还原电位的现场测试可以得出：（1）该研究区所处特殊的地理位置（青藏高原的东南部-横断山系北段,属川西高山高原区）导致该区具有冬长,无夏,春秋短,气温低,温差大等独有的气象条件;该区主要的构造侵蚀高山地貌类型导致地下水循环具有径流途径短,水力坡度大,水-土间交换作用十分强烈的特点,该区土壤的特点是淋滤作用较强且成弱酸性等,这三个环境要素的特点是直接导致该区饮用水中氧化还原电位值升高的主要原因;（2）由于不同类型水（河水、沟水、泉水、土井水）其与大气接触程度的差异导致其氧化还原值呈现由高到低的趋势,即河水〉沟水〉泉水〉土井水。     

A Study of DMS Oxidation in the Tropics: Comparison of Christmas Island Field Observations of DMS, SO2, and DMSO with Model Simulations

This study reports comparisonsbetween model simulations, based on current sulfurmechanisms, with the DMS, SO₂ and DMSOobservational data reported by Bandy et al.(1996) in their 1994 Christmas Island field study. For both DMS and SO₂, the model results werefound to be in excellent agreement with theobservations when the observations were filtered so asto establish a common meteorological environment. Thisfiltered DMS and SO₂ data encompassedapproximately half of the total sampled days. Basedon these composite profiles, it was shown thatoxidation of DMS via OH was the dominant pathway withno more than 5 to 15% proceeding through Cl atoms andless than 3% through NO₃. This analysis wasbased on an estimated DMS sea-to-air flux of 3.4 ×10⁹ molecs cm^-2 s^-1. The dominant sourceof BL SO₂ was oxidation of DMS, the overallconversion efficiency being evaluated at 0.65 ± 0.15. The major loss of SO₂ was deposition to theocean's surface and scavenging by aerosol. Theresulting combined first order k value was estimated at 1.6 × 10^-5 s^-1. In contrast to the DMSand SO₂ simulations, the model under-predictedthe observed DMSO levels by nearly a factor of 50. Although DMSO instrument measurement problems can notbe totally ruled out, the possibility of DMSO sourcesother than gas phase oxidation of DMS must beseriously considered and should be explored in futurestudies.     

Sulfur Isotopic Study of the Toyoha Deposit, Hokkaido, Japan Comparison between the Earlier-Stage and the Later-Stage Veins

Abstract: The sulfur isotopic ratios (δ³⁴S) of ore minerals from the Toyoha deposit, Hokkaido, one of the largest Pb–Zn–Ag polymetallic vein-type deposits in Japan, were studied. More than 90% of the δ³⁴S values of the studied sulfide minerals collected from the Toyoha deposit range from +5 to +9%, with an average of approximately +7% irrespective of the mineral species, veins, elevations, depth, mineralization stages and mineral assemblages. Relatively uniform δ³⁴S values obtained in this study suggest that the reduced aqueous sulfur species predominated over the oxidized sulfur in the ore solution throughout the mineralization stages. Thus, the source of sulfur for the ore sulfides is postulated to be magmatic.
The temperature obtained from the fluid inclusion study and the temperature of the sulfur isotopic geothermometer are not consistent. This suggests that each mineral precipitated under disequilibrated conditions with respect to the sulfur isotope.
The change in redox conditions presumably encountered between the mineralization stages did not account for the isotopic fluctuations since the isotopic exchanges between the oxidized and reduced aqueous sulfurs are much slower than the rate of oxidation of the ore solution.