Development and Extension of Seawater Desalination by Reverse Osmosis

Seawater desalination has been people‘s fond dream since ancient times,the dream is now becoming a reality.This paper presents a brief development history of reverse osmosis.Much attention was paid to innovative development in mebranes,modules.equipments and applied technology,including asymmetric and composite membranes,spiral-wound element and hollow fiber module,energy recovery equipments and different technological processes.The extension of reverse osmosis,such as desalination,pre-concentration,integrated processes and nanofiltration,is also briefly mentioned.     

首都圈地区现今断层活动的数学模拟及地震危险性讨论

以首都圈地区现今活动断层上近２０年的位移测量资料为依据，用二维线弹性有限元对该区断层的活动特征进行了拟合，并结合有关资料讨论了该区的地震危险性。结果表明：１９７７－１９８６年间该区主压应力优势方位与华北较一致，约为Ｎ４５°－８０°Ｅ；１９８６－１９９０年其主压应力方向向北偏转，约为Ｎ５°－６０°Ｅ；１９９０年至现在其主压应力又向东偏转，角度大于第一阶段，约为Ｎ８０°－９５°Ｅ。该区的张家口－延庆一带近期有发生中强震的可能；丰镇－阳高－大同地区和凉城－古营盘地区应力较高，也应引起注意。     

Timing of UHP metamorphism in the Hong’an area,western Dabie Mountains,China: evidence from zircon U–Pb age,trace element and Hf isotope composition

The Hong’an area (western Dabie Mountains) is the westernmost terrane in the Qinling-Dabie-Sulu orogen that preserves UHP eclogites. The ages of the UHP metamorphism have not been well constrained, and thus hinder our understanding of the tectonic evolution of this area. LA-ICPMS U–Pb age, trace element and Hf isotope compositions of zircons of a granitic gneiss and an eclogite from the Xinxian UHP unit in the Hong’an area were analyzed to constrain the age of the UHP metamorphism. Most zircons are unzoned or show sector zoning. They have low trace element concentrations, without significant negative Eu anomalies. These metamorphic zircons can be further subdivided into two groups according to their U–Pb ages, and trace element and Lu–Hf isotope compositions. One group with an average age of 239 ± 2 Ma show relatively high and variable HREE contents (527 ≥ Lu_N ≥ 14) and ¹⁷⁶Lu/¹⁷⁷Hf ratios (0.00008–0.000931), indicating their growth prior to a great deal of garnet growth in the late stage of continental subduction. The other group yields an average age of 227 ± 2 Ma, and shows consistent low HREE contents and ¹⁷⁶Lu/¹⁷⁷Hf ratios, suggesting their growth with concurrent garnet crystallization and/or recrystallization. These two groups of age are taken as recording the time of prograde HP to UHP and retrograde UHP–HP stages, respectively. A few cores have high Th/U ratios, high trace element contents, and a clear negative Eu anomaly. These features support a magmatic origin of these zircon cores. The upper intercept ages of 771 ± 86 and 752 ± 70 Ma for the granitic gneiss and eclogite, respectively, indicate that their protoliths probably formed as a bimodal suite in rifting zones in the northern margin of the Yangtze Block. Young Hf model ages (T _DM1) of magmatic cores indicate juvenile (mantle-derived) materials were involved in their protolith formation. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

An experimental study of the grain-scale processes of peridotite melting: implications for major and trace element distribution during equilibrium and disequilibrium melting

The grain-scale processes of peridotite melting were examined at 1,340°C and 1.5 GPa using reaction couples formed by juxtaposing pre-synthesized clinopyroxenite against pre-synthesized orthopyroxenite or harzburgite in graphite and platinum-lined molybdenum capsules. Reaction between the clinopyroxene and orthopyroxene-rich aggregates produces a melt-enriched, orthopyroxene-free, olivine + clinopyroxene reactive boundary layer. Major and trace element abundance in clinopyroxene vary systematically across the reactive boundary layer with compositional trends similar to the published clinopyroxene core-to-rim compositional variations in the bulk lherzolite partial melting studies conducted at similar P–T conditions. The growth of the reactive boundary layer takes place at the expense of the orthopyroxenite or harzburgite and is consistent with grain-scale processes that involve dissolution, precipitation, reprecipitation, and diffusive exchange between the interstitial melt and surrounding crystals. An important consequence of dissolution–reprecipitation during crystal-melt interaction is the dramatic decrease in diffusive reequilibration time between coexisting minerals and melt. This effect is especially important for high charged, slow diffusing cations during peridotite melting and melt-rock reaction. Apparent clinopyroxene-melt partition coefficients for REE, Sr, Y, Ti, and Zr, measured from reprecipitated clinopyroxene and coexisting melt in the reactive boundary layer, approach their equilibrium values reported in the literature. Disequilibrium melting models based on volume diffusion in solid limited mechanism are likely to significantly underestimate the rates at which major and trace elements in residual minerals reequilibrate with their surrounding melt. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Simple models for dynamic melting in an upwelling heterogeneous mantle column: Analytical solutions

Several lines of evidence suggest that the melt generation and segregation regions of the mantle are heterogeneous, consisting of chemically and lithologically distinct domains of variable size and dimension. Partial melting of such heterogeneous mantle source regions gives rise to a diverse range of basaltic magmas. In order to better assess the role of source heterogeneity during mantle melting, we have undertaken a theoretical study of trace element distribution and fractionation during concurrent melting and melt migration in an upwelling, chemically heterogeneous, two-porosity double lithology melting column. Analytical solutions for the abundance of a trace element in the matrix and channel were obtained under the assumptions that the porosity, melt and solid velocities, and solid-melt partition coefficients are constant and uniform. For simplicity, we neglected diffusion and dispersion in the melt. Chemical source heterogeneities of arbitrary size and shape were integrated into the simple melting models by allowing trace element abundance in the source region to vary as a function of time and space. Concurrent melting and melt migration in an upwelling heterogeneous mantle may be approximated as a quasi-steady state problem in which time-dependent concentration patterns produced by melting of heterogeneous source regions are superimposed on a reference steady-state concentration distribution established by melting of the ambient or background mantle. Chromatographic fractionation is especially important for the matrix melt and solid when chemical heterogeneities are involved during melting and melt migration in the mantle, giving rise to significant phase-shift between two incompatible trace elements in the matrix melt and scattered correlations among incompatible trace elements in residual peridotites. Mixing is the chief mass transfer process in the dunite channel where the chromatographic effect is negligible for most of the incompatible trace elements. The lack of chromatographic fractionation among incompatible trace elements and isotopic ratios in MORB suggests either most MORB are channel melts or mixing in magma conduit and chamber is very efficient such that the phase-shift is averaged out during magma transport and storage processes. Advection brings melt produced by smaller-degree of melting in the deeper part of the melting column to the overlying melting region, increasing the incompatible trace element abundance in the matrix and the channel. This advection-induced self-enrichment is especially important when heterogeneous sources are involved and may account for some of the enriched incompatible trace element patterns observed in residual peridotite that were previously interpreted to be a result of mantle metasomatism. Systematic studies of high-resolution spatially correlated mantle samples may help to constrain the melting history and the size and nature of chemical heterogeneities in the mantle.     

晚三叠世松潘甘孜和川西前陆盆地的物源对比：构造演化和古地理变迁的线索

为了研究龙门山褶皱冲断带两侧的松潘甘孜和川西前陆盆地在大地构造和沉积学方面存在的联系,笔者等分别在松潘甘孜东缘马尔康—理县地区和川西前陆盆地都江堰地区进行了采样和碎屑锆石的LAICPMS UPb定年工作。269颗锆石的定年结果显示,中—晚三叠世拉丁期—诺利期松潘甘孜复理石盆地东缘沉积地层中的碎屑锆石年龄主要集中在250~280 Ma、1800~1900 Ma和2400~2500 Ma、200~245 Ma、400~450 Ma,对应的物源主要为东昆仑岛弧、华北陆块基底、义敦岛弧以及北秦岭。与之相比,川西前陆盆地诺利期—瑞替期的须家河组地层中的碎屑锆石年龄大致主要集中在1800~1900 Ma和2400~2500 Ma、720~850 Ma、950~1200 Ma、400~450 Ma。该统计结果总体上继承了松潘甘孜数据体的特征,揭示出须家河组物源来自西部——松潘甘孜褶皱带的再旋回沉积和龙门山前陆冲断带。     

牛庄洼陷沙河街组超压系统发育特征及其演化

东营凹陷牛庄洼陷沙河街组发育有超压系统,这对油气运移和聚集过程有着重要的影响。在对超压系统现今发育特征研究的基础上,本文运用约束下数值模拟方法对牛庄洼陷超压系统的演化规律进行研究,并探讨了超压系统的主要形成机制。牛庄洼陷在沙河街组四段、沙河街组三段的下亚段和中亚段存在着超压系统,最大压力系数可以达到1.8,最大剩余压力超过了20MPa。自沙三段上亚段沉积期开始,超压系统开始发育。到东营组沉积期末,超压系统经历了大约10Ma的泄压过程。自新近系馆陶组沉积期,超压系统再次迅速增压,逐渐接近现今发育状况。上覆地层沙三段上亚段高沉积速率导致了超压系统的形成和早期剩余压力的增加,而水热增压和烃类物质大量生成联合造成超压系统晚期迅速增压。超压系统演化规律揭示出在油气主要运移期研究区古异常流体压力的分布状况,这为进一步开展牛庄洼陷油气运移和聚集过程的动力学研究提供了理论依据。     

库车坳陷东部山前带古近系不同体系域内扇三角洲沉积砂体的对比研究

通过对塔里木盆地库车坳陷南天山山前带克孜勒努尔沟与依奇克里克野外露头沉积相的精细研究,结合山前带大量地震剖面分析与迪那201井、东秋5井等多口钻井测井相和岩心精细描述,将古近系库姆格列木群划分为2个层序。层序2低位域以冲积扇沉积为主,自湖侵体系域始,研究区广泛发育退积与进积型扇三角洲沉积。库姆格列木群层序2湖侵体系域内扇三角洲平原砂体以正韵律沉积为主,砂砾岩占地层厚度的(68.4～87)%;扇三角洲前缘砂体正、反韵律均有分布,砂砾岩占地层的百分比有所降低,为(55.2～77)%。高位体系域内主要发育以反韵律砂体为主的扇三角洲前缘沉积。古近系苏维依组只发育一个层序,其低位体系域的砂体为扇三角洲平原与前缘的分流河道砂体,湖侵体系域内扇三角洲前缘砂体正、反韵律均发育,高位体系域内主要发育扇三角洲前缘沉积,以反韵律砂体为主,正韵律砂体相对较少。对比苏维依组不同体系域内砂体储集性,湖侵域内砂体优于高位域内砂体。扇三角洲沉积体中有利储集砂体首选为湖侵体系域内的扇三角洲前缘水下分流河道和河口坝砂体,次之为低位域扇三角洲前缘(平原)分流河道砂体,最后是高位域内的河口坝及席状砂沉积砂体。特别要指出:低位体系域或者湖侵体系域底部发育的扇三角洲前缘(平原)分流河道砂体(底砂砾岩)被快速湖侵的较厚的暗色泥岩所覆盖,可形成较好储集场所。     

祁连山近期七一冰川融水径流特征分析

利用2006年8月1日-9月30日的实测水文数据,对"七一"冰川融水径流产汇流特征进行了分析,并揭示出该冰川日消融特征.通过对冰川融水量的估算以及径流模数的计算,并与过去的观测结果进行对比,表明近些年来"七一"冰川消融强度和消融量都在增大,而且2006年消融量为近几年观测的最大值.虽然不同年份消融量不一样,但"七一"冰川总的趋势是一直处于萎缩状态,随着全球变暖,"七一"冰川的萎缩可能将继续下去.通过对设立在沿冰川下游方向两个不同的水文断面进行对比分析,结果表明"七一"冰川融水径流在向下游运动过程中有部分水入渗为河谷潜流,观测期内两个相距不到2 km的水文断面间渗漏损耗占近1/3左右.