反向VSP透射层析成像法在岩墙松动层检测中的应用

通过实例介绍了反向VSP透射层析成像方法的基本原理、数据采集和资料处理方法。利用该方法在检测岩墙松动层厚度中取得了很好的勘探效果。     

不同酸液条件下叙利亚灰岩溶蚀能力的实验研究

文章根据SY/T 6526-2002《盐酸与碳酸盐岩动态反应速率测定方法》,利用高温高压酸岩反应仪进行了普通盐酸、有机盐酸、胶凝酸、乳化酸和地面交联酸与叙利亚灰岩粉末在两个目的层温度95 ℃和150 ℃下2.0 h的溶蚀实验。结果显示,五种酸液2.0 h的酸溶解率都在90%以上,普通盐酸、有机盐酸的溶蚀能力高于胶凝酸、乳化酸和地面交联酸三种缓速酸;95 ℃下乳化酸和地面交联酸溶解慢、溶解率低,而150 ℃下是地面交联酸和胶凝酸;适当条件下,“多相隔离”对H+抑制作用要比高粘度溶液强,而且随着酸液内部高分子之间链接复杂程度的提高,H+被束缚的程度也增大;温度提高增大了酸溶解率,对乳化酸、地面交联酸和胶凝酸影响比较显著,对普通盐酸和有机盐酸不明显。      

A Preliminary Study on the Present Crustal Stress of Northern South China Sea

<正>The South China Sea(SCS)is the largest marginal sea in West Pacific formed by a combined effect of the Eurasian plate,Pacific plate and India-Australian plate,and is thus considered to be a unique natural laboratory to study oceanic dynamics and tectonic evolutions(Xie et al.,2006;Luan and Zhang,2009).Besides,the SCS contains enormous petroleum resources for its favorable conditions of oil-gas generation,accumulation and preservation.It is therefore imperative to intensively study the marine in-situ     

Adsorption of phenanthrene on Al (oxy)hydroxides formed under the influence of tannic acid

Although there has been substantial research done on adsorption of metals/metalloids by Al (oxy)hydroxides, little is known regarding the adsorption of polyaromatic hydrocarbons (PAHs) on Al (oxy)hydroxides, especially those formed in the presence of organic acid. This paper investigated the adsorption of phenanthrene on Al (oxy)hydroxides formed with initial tannate/Al molar ratios (MRs) 0, 0.001, 0.01, and 0.1 (referred to MR0, MR0.001, MR0.01, and MR0.1, respectively) through batch adsorption experiments and FTIR study. The results showed that Al (oxy)hydroxides were important sorbents for phenanthrene. The adsorption kinetic data were fitted well with the pseudo-second-order equation. According to a modified Freundlich model, the adsorption capacities of Al (oxy)hydroxides followed a descending order of MR0.1 > MR0 ≥ MR0.01 > MR0.001, which was inconsistent with the organic carbon content in the Al (oxy)hydroxides. Adsorption capacity correlated with the specific surface area, micropore area, and micropore diameter of Al (oxy)hydroxides, yet the relationships were not statistically significant (P > 0.05). FTIR results showed that physical interaction was essential in phenanthrene adsorption onto the Al (oxy)hydroxides, which could be explained by an entropy-driven process. Surface hydrophobicity of Al (oxy)hydroxides played a key role in phenanthrene adsorption. Additional π–π electron donor–acceptor interaction of phenanthrene (acting as electron donor) with aromatic ring of tannic acid (electron acceptor) could be also important in phenanthrene adsorption by high MR Al (oxy)hydroxides, yet it needs further study. The findings obtained in the present study are of fundamental significance in understanding the mechanism of immobilization of PAHs in low organic matter but oxide-rich soils.     

点苍山-哀牢山变质杂岩带变沉积岩的变质演化

点苍山-哀牢山变质杂岩带位于青藏高原东南缘大理-元江-元阳-河口一带,出露规模达数百千米,是扬子板块和印支陆块之间的一条重要构造带.该变质杂岩带主要由各类正片麻岩、副片麻岩、大理岩所组成,夹有斜长角闪岩、石榴辉石岩和超镁铁质岩石的透镜体或团块.其中,变沉积岩如含夕线石和蓝晶石的片麻岩类岩石保存了多阶段的矿物组合及异常复杂的矿物相转变关系.详细的岩相学、成因矿物学以及矿物相转变关系分析表明,变沉积岩系经历了早期进变质阶段(M1)、峰期角闪-麻粒岩相变质阶段(M2)、峰后近等温减压(脱水熔融)阶段(M3)以及晚期退变质阶段(M4)的变质演化.其中,M1阶段的稳定矿物组合为石榴石+斜长石+白云母+石英+十字石±蓝晶石±黑云母±钾长石,M2阶段的稳定矿物组合为石榴石+黑云母+蓝晶石/夕线石+斜长石+石英、石榴石+黑云母+斜长石+石英±钾长石±夕线石,M3阶段的共生矿物组合为石榴石+黑云母+夕线石+斜长石+石英,M4阶段的矿物组合为黑云母+白云母+斜长石+石英±钾长石±石榴石等.通过传统GB-GASP温压计和二云母温度计的估算结果,配合P-T视剖面定量计算,确定早期进变质阶段(M1)的温压条件为T=560 ～ 590℃,P=5.5 ～6.3kb,峰期角闪-麻粒岩相阶段(M2)的温压条件为T=720～ 760℃、P=8.0～9.3kb,峰后近等温减压阶段(M3)的温度压力条件为T=640～760℃,P=5.0～7.3kb,晚期退变阶段(M4)的温压条件为T=521～648℃,P=4.0～5.0kb.上述研究结果表明,点苍山-哀牢山变沉积岩记录了典型碰撞造山带型式的顺时针P-T演化轨迹,表明点苍山-哀牢山变质杂岩带的形成与印度板块和欧亚板块之间的俯冲-碰撞存在密切的成因关系.     

华南地块西南缘格林威尔期区域构造解析

从构造变形的角度入手,通过观察华南地块西南缘前震旦纪各岩石单元野外露头上的变形特征,运用构造解析方法,识别出不同期次变形构造的形态和位态特征及其在空间上的组合关系,划分变形构造的世代,结合近年来年代学研究成果,确定不同期次变形构造形成时代。研究表明,在华南地块西缘基底岩石单元中,发育格林威尔期的变形构造,其构造形迹东西向展布,该期构造变形的强度,在康滇地区各岩石单元中具有不均匀性,在野外露头上见到的格林威尔期小型紧闭、倒转褶皱主要分布在攀枝花周边的基底岩石单元中,而其南部的滇中地区,同期的褶皱构造相对较弱。根据格林威尔期构造位态特征,推断形成该期变形构造的构造运动方向为南北向的挤压运动。     

阿尔金断裂新生代活动方式及其与柴达木盆地的耦合分析

位于青藏高原北缘的阿尔金左旋走滑断裂是世界上规模最大也是最重要的线性构造之一,其新生代以来的活动方式是限定高原生长机制的重要边界条件.本文在对阿尔金山中不同方向隆起构造进行分析的基础上,综合前人资料论证了阿尔金断裂在晚始新世-中中新世时以基底剪切为主,大规模地表走滑则发生在中中新世以后.对柴达木盆地内近东西向和北西向断裂系统的分布、形态、活动时间进行了详细的分析,发现它们是在不同时间、不同区域、不同控制条件下形成的两套断裂系统,与阿尔金断裂的两阶段活动方式存在很好的耦合关系.柴达木盆地西北侧的沉积和构造特征表明阿尔金山的隆升幅度和范围在中中新世达到最大,随后则逐渐减小,这种变化也与阿尔金断裂从基底剪切到地表走滑的转换非常吻合.     

论地震数值预报——关于我国地震预报研究发展战略的思考

随着中国工业化和社会现代化进程的加快 ,中国城市化进程必将进一步加速。如何减轻地震灾害的问题正变得日益严峻。尽管地震预测是一个举世公认的国际性科学难题 ,但在强化各种减轻地震灾害措施的同时 ,仍须大力推进地震预测研究。为此 ,需要打破长期徘徊在以地震前兆异常监测为基础的经验性预测局面 ,把注意力尽快转向研究以动力学为基础的数值预报。以GPS为代表的空间对地观测技术 ,岩石圈巨型高分辨率宽频带流动地震台阵观测技术以及数值模拟技术已经为地震数值预报研究提供了前所未有的技术基础。以地震数值预报为目标的GPS阵列地壳形变连续观测 ,高分辨率地壳上地幔结构探测 ,地壳动力学 ,地震孕育和破裂过程的理论、模拟试验和实际观测 ,数据同化和计算软件的开发应成为今后研究的重点。现在的问题是 ,需要积极借助数值天气预报的经验 ,强化多学科 ,多部门的组织协调 ,尽早在有条件的地区开展地震动力学数值预报的科学试验。地震数值预报研究必将极大地促进中国地震科学基础研究和地震预报的进一步发展。     

Pretreatment of high strength waste emulsions by combined vibratory shear enhanced process with Fenton oxidation

Pretreatment of waste emulsions with high organic content by a combined process of vibratory shear enhanced process and Fenton’s oxidation prior to biological treatment was investigated. Vibrating membrane had shown good performance in chemical oxygen demand and oil removals and the mitigation of concentration polarization. However, the permeate after filtration processing still contained high content of organics. Thus, additional Fenton oxidation was applied to reduce the organic loading, and improve the biodegradability of the wastewater. The optimal molar ratio of ferrous iron to hydrogen peroxide was 0.05 obtained from the jar-test experiments. Removal of organics was enhanced by increasing hydrogen peroxide dosage, while efficiency of hydrogen peroxide reached maximum of 1.11(w/w) at the hydrogen peroxide dosage of 6.8 g/L. Furthermore, the biological experiments indicated that the high concentration of organics could inhibit microbial activity, which decreased the chemical oxygen demand degradation rates. The adaptive period of the microbe was greatly shortened using Fenton’s reagent at the low dosages. The improvement of the biodegradability could be explained by partial mineralization and chemical transformation of parent organic compounds after Fenton oxidation.