从平衡-封闭-静态转向非平衡-开放-动力学研究-热液矿床成因的若干新概念概述

热液金属矿床成因研究过程中,观测与实验始终是密切结合的。上世纪70年代,平衡热力学的实验数据的快速积累,使人们用热力学理论计算可以预测和反演矿石和岩石的成因。但是,没有矿物-水溶液的反应速率数据,又没有与流体力学的结合,搞清楚矿石成因是困难的。七、八十年代,开始研究矿物与水溶液的反应动力学实验。科学家们开始瞄准了从平衡-封闭-静态转向非平衡-开放-动力学研究的这个大方向。1992年我们建立地球化学动力学开放研究实验室。研究高温高压矿物与水反应速率,发现固液的开放体系的自组织现象。实验发现温度影响矿物的各个元素反应速率改变,发现在跨越水临界态时矿物与水反应速率涨落、在近临界的气-液两相不混溶区一些金属进入气相、超临界流体的氧化作用及特别的溶剂性能影响矿物溶解性质。实验证实:临界态区流体与矿石成因有关。水岩相互作用的反应动力学实验温度从低温到550度,揭示矿石的金属来源、迁移、金属与蚀变分带机制。一大批大于300度的矿物与水反应动力学实验在国际界是少有报道的。九十年代,超高压的科学发展,与同步辐射光源的技术进步的结合,使固体地球科学又迈向了地球深内部。我们发展了高温高压流体性质的原位直测(测量850℃水溶液)红外谱,发现深部流体的新性质:气液两相流体的新结构,在临界温度区(300~400℃),水分子氢键网络的破坏受压力影响不大(23MPa~3GPa),同时,出现水的高电导率。研发新仪器为开放-流动-非平衡的反应动力学实验与极端条件下物质性质的直接观测结合,在科学前沿领域开辟了创新道路。     

SAR影像与光学影像的高斯伽玛型边缘强度特征匹配法

提出了一种基于影像边缘强度图描述的SAR影像与光学影像匹配方法。首先对影像进行粗纠正,消除影像之间的尺度和旋转变化;其次,改进相位一致性特征检测方法,提取对影像相干斑噪声稳健的特征点;然后基于高斯伽玛型双边窗口比值算子计算影像边缘强度图,在此基础上构造不变特征描述符;最后联合几何约束条件,实现SAR影像与光学影像匹配。试验结果证明,与现有方法相比,本文方法能够大幅提高SAR影像与光学影像匹配结果中的正确匹配特征数量以及影像配准精度。     

一种四叉树和测地线活动轮廓模型相结合的海陆影像分割方法

海陆影像分割对于后续的海岸线提取、潮间带地形反演、海岸演化状况分析等都具有十分重要的意义。本文在分析了四叉树、测地线活动轮廓(GAC)模型和Canny边缘检测算子等在海陆影像分割中优缺点的基础上,提出了一种四叉树、Canny算子和GAC模型相结合的海陆影像分割方法。该方法综合利用上述各方法的优点,将Canny算子边缘检测结果融入到基于四叉树初分割的GAC模型中,重构边界停止函数,演化水平集方程,实现海陆影像分割。试验结果表明,该方法具有海陆影像分割速度快、精度高、可靠性强和自动化程度高等优点,对于弱边缘以及严重凹陷边缘,都能实现自动和准确分割。     

Reactivity of micas and cap-rock in wet supercritical CO2 with SO2 and O2 at CO2 storage conditions

Seal or cap-rock integrity is a safety issue during geological carbon dioxide capture and storage (CCS). Industrial impurities such as SO₂, O₂, and NOx, may be present in CO₂ streams from coal combustion sources. SO₂ and O₂ have been shown recently to influence rock reactivity when dissolved in formation water. Buoyant water-saturated supercritical CO₂ fluid may also come into contact with the base of cap-rock after CO₂ injection. Supercritical fluid-rock reactions have the potential to result in corrosion of reactive minerals in rock, with impurity gases additionally present there is the potential for enhanced reactivity but also favourable mineral precipitation.The first observation of mineral dissolution and precipitation on phyllosilicates and CO₂ storage cap-rock (siliciclastic reservoir) core during water-saturated supercritical CO₂ reactions with industrial impurities SO₂ and O₂ at simulated reservoir conditions is presented. Phyllosilicates (biotite, phlogopite and muscovite) were reacted in contact with a water-saturated supercritical CO₂ containing SO₂, or SO₂ and O₂, and were also immersed in the gas-saturated bulk water. Secondary precipitated sulfate minerals were formed on mineral surfaces concentrated at sheet edges. SO₂ dissolution and oxidation resulted in solution pH decreasing to 0.74 through sulfuric acid formation. Phyllosilicate dissolution released elements to solution with ∼50% Fe mobilized. Geochemical modelling was in good agreement with experimental water chemistry. New minerals nontronite (smectite), hematite, jarosite and goethite were saturated in models. A cap-rock core siltstone sample from the Surat Basin, Australia, was also reacted in water-saturated supercritical CO₂ containing SO₂ or in pure supercritical CO₂. In the presence of SO₂, siderite and ankerite were corroded, and Fe-chlorite altered by the leaching of mainly Fe and Al. Corrosion of micas in the cap-rock was however not observed as the pH was buffered by carbonate dissolution. Ca-sulfate, and Fe-bearing precipitates were observed post SO₂-CO₂ reaction, mainly centered on surface cracks and an illite rich illite-smectite precipitate quantified. Water saturated impure supercritical CO₂ was observed to have reactivity to rock-forming biotite, muscovite and phlogopite mineral separates. In the cap-rock core however carbonates and chlorite were the main reacting minerals showing the importance of assessing actual whole core.     

川东长兴组台缘礁滩相储层纵向非均质性特征及形成机制——以川东宣汉盘龙洞长兴组剖面为例

近几年,随着四川盆地海相碳酸盐岩储层勘探的不断加强,碳酸盐岩储层强的非均质性已成为制约礁滩气藏勘探开发的现实问题。以川东宣汉盘龙洞长兴组典型台缘礁滩剖面为研究对象,通过对典型台缘礁滩野外剖面的精细观察,结合镜下薄片及岩矿资料分析,重点探讨了盘龙洞礁滩储层纵向非均质性特征及成因。剖面上礁滩体垂向上存在很强的旋回性和储层非均质性,其储集岩分布、储层厚度、白云岩化程度、溶蚀作用等受海平面周期性的升降变化影响而呈现周期性变化。礁滩储层非均质性受高能相带、海平面升降变化和建设性成岩作用的共同控制,高能相带控制储层原生孔隙的发育,决定了储层的沉积非均质性,白云岩化和溶蚀作用有利于礁滩体储层的形成,大气淡水淋滤改造对于优化储层具有关键作用,海平面升降变化决定了礁滩体旋回性发育,而建设性成岩作用的选择性改造深化了储层非均质性。     

新疆西昆仑汗铁热克一带侏罗纪沉积相与沉积环境分析

新疆西昆仑汗铁热克一带地处塔里木盆地西南缘,构造上属塔里木盆地与西昆仑造山带的结合部位,侏罗纪地层包括积莎里塔什组、康苏组、扬叶组、塔尔尕组和库孜贡苏组。根据岩性、颜色、粒度分析及沉积相标志等方法,将汗铁热克一带侏罗纪沉积环境与沉积相划分为冲积扇、扇三角洲和湖泊相,其沉积特征为侏罗纪早期快速充填,中期稳定沉降,晚期短暂的沉积间断后充填,并系统分析了研究区在整个侏罗纪沉积环境演化规律。     

压力对辉长岩矿物反应和部分熔融影响的实验研究

本文在高温高压条件下,开展了辉长岩矿物反应与部分熔融实验,利用偏光显微镜与扫描电镜对实验样品微观结构观察,研究实验中的新生矿物与熔体的分布;通过电子探针分析熔体成分特征。实验结果表明,在低压(300MPa)条件下,静压和塑性变形实验样品中,单斜辉石以固体反应方式生成橄榄石,在高压(1300MPa)塑性实验中所有实验样品都没有发现新生矿物颗粒,这与相图中低压条件下斜长石与橄榄石稳定共存,而高压下斜长石-辉石稳定共存相吻合。高压塑性变形条件下,单斜辉石和黑云母首先发生部分熔融,随着温度增高,斜长石逐渐参与熔融,熔体呈薄膜状分布在矿物颗粒边界,熔体成分依赖于参与熔融的矿物成分,表明出现的熔体为非平衡熔融结果。     

广西大瑶山东南缘侏罗纪埃达克质花岗岩的特征、成因及构造意义

对钦杭结合带西南段大瑶山东南缘的中晚侏罗世埃达克质花岗岩（165~153 Ma）进行了岩石学、地球化学研究,并探讨了埃达克质和TTG岩类的特征属性。岩石SiO₂含量63.76%~72.13%,总体具高Al₂O₃（Al₂O₃≥15%）、低MgO （<3%）,亏损重稀土元素（HREE）、正Eu异常或弱的负Eu异常,低Y （≤18×10^-6）和Yb （≤1.9×10^-6）,高Sr （>300×10^-6）和Sr/Y值（>20）等埃达克岩独特的地球化学特征。结合区域构造演化分析认为,该侏罗纪埃达克质花岗岩形成于陆内伸展构造背景,为大陆板内加厚（隆起区）的下地壳底部岩石部分熔融的产物,属大陆板内环境I型花岗岩。具有类似于低镁安山岩/闪长岩系列（LMA）和镁安山岩/闪长岩系列（MA）两种高压型TTG亚类的属性,为古俯冲增生带下地壳弧型岩石熔融的继承性特征,与中生代古太平洋俯冲板片熔融过程无关,属非俯冲成因的埃达克/TTG岩类。其空间上与大瑶山东南缘早古生代俯冲增生带高度重合,且与早古生代TTG侵入岩组合紧密相邻,提示它们可能源自于早古生代洋壳俯冲带或大陆边缘弧下地壳玄武质岩石的部分熔融,因而具有洋俯冲成因的特征属性。     

Adsorption of Pentachlorophenol onto Oxide and Clay Minerals： Surface Reaction Model and Environmental Implications

The adsorption of pentachlorophenol （PCP） onto quartz, kaolinite, illite, montmorillonite and iron oxides has been investigated by batch equilibrium techniques. The pH-dependent isotherms are curves with peak values, the position of which is at about pH = 5-6 depending on the mineral species. Based on distribution of both speciation of surface hydroxyls on minerals and PCP in solution a surface reaction model involving surface complexation and surface electrostatic attraction is presented to fit the pH-dependent isotherms, and both reaction constants are calculated. The results show that on quartz and phyllosilicate minerals the predominant adsorption reaction is surface complexation, meanwhile both of surface electrostatic attraction and surface complexation are involved on the iron oxide minerals. The reaction constants of surface electrostatic adsorption are usually one to three orders in magnitude, larger than that of surface complexation. The concentration-dependent isotherms can be well fitted by Langmnir equation with the correlation coefficient R〉0.93 for kaolinite and iron oxides. The maximum adsorption is found in the order： hematite 〉 lepidocrocite 〉 goethite 〉 kaolinite 〉 quartz 〉 montmorillonite ≈ illite, which can be interpreted by consideration of both reaction mechanism and surface hydroxyl density. The significant adsorption of PCP onto mineral surfaces suggests that clay and iron oxide minerals will play an important role as HIOCs are adsorbed in laterite or latertoid soil, which is widespread in South China.     

基于分段副产物瞬时选择性的反应器网络综合

针对第三类反应体系的反应器网络综合问题,提出将串联反应以反应物到目的产物的反应步数为依据的新分段策略。通过比较不分段目的产物、不分段目的产物和中间产品、分段副产物和分段目的产物这四种不同的瞬时选择性,提出以分段副产物瞬时选择性为参数,以其对关键组分浓度或转化率的导数为依据选择各阶段最合适的反应器,以目的产物总选择性最大为目标采用遗传算法优化反应器网络。通过三个实例验证了本文所建立方法在解决复杂反应反应器网络综合问题的有效性,且本方法同样适用于简单反应体系。