金属矿物的反应动力学与地球化学意义

概述了动力学实验的技术方法和金属矿物的反应动力学研究进展。动力学实验使用的三种基本化学反应装置是间歇反应器（ＢＲ）、活塞流反应器（ＰＦＲ）和混合流反应器（ＭＦＲ）,确定速率定律的数学方法包括积分法、微分法和混合法,以微分法中的初始速率法应用最广。目前主要研究了水溶液中黄铁矿氧化、黄铁矿和黄铜矿形成、晶质铀矿和磁铁矿溶解的速率定律和反应机理,发现：（１）酸性溶液中黄铁矿的氧化速率对Ｆｅ３＋和Ｏ２浓度呈分数依赖并受表面反应的控制;（２）低于３００℃时黄铁矿不能从溶液中直接成核,而需初始地通过ＦｅＳ先驱物的硫化生成,ＦｅＳ与Ｈ２Ｓ反应形成黄铁矿的速率方程为二级;（３）磁黄铁矿或黄铁矿与Ｃｕ２＋反应均可形成黄铜矿,前者经历了一系列准稳的Ｃｕ Ｆｅ硫化物的中间物,后者的速率方程为表观一级并受表面反应的控制;（４）酸性ｐＨ时磁铁矿的非线性溶解行为可采用表面反应扩散输运耦合的收缩核模型（ＳＣＭ）来描述。有关动力学实验成果完善和深化了对矿床中黄铁矿、黄铜矿的形成机理和风化壳中磁铁矿的稳定性等方面的认识。将来的实验研究将向更多的金属矿物和高温高压领域发展。     

Multi-stage pseudomorphic replacement of garnet during polymetamorphism: 2. Algebraic analysis of mineral assemblages

Chemical relationships among four metapelites have been studied by investigation of mineral and bulk chemistry data and by singular value decomposition analysis of single and composite assemblage matrices. Bulk rock compositions cluster close together in an AFM diagram, all within the intersection space defined by the four sample assemblages. The similarity of bulk compositions normalized on a silica-free, anhydrous basis indicates that sample chemistries differ mainly as a result of inhomogeneous distribution of quartz layers. The existence of mass balance relationships among samples indicates that assemblages also overlap in the Si–Ti–Al–Fe–Mg–Mn–Ca–Na–K multisystem. Analysis of single and composite matrices helps in defining possible mass balances linking sample mineral facies to one another during progressive contact metamorphism. The assemblage in sample A can form as the result of the model reaction 5.000  Ky+0.269 Grt+0.965 Bt+0.314 Pl=0.049 Ilm+1.115 Ms+0.849 Chl+0.306 St and react to assemblage B via reaction 0.97 Chl+0.52 Grt+0.66 Ms+0.14 Ilm+1.26  Ky=0.42 St+0.63 Bt+0.22 Pl coupled with the Ky→And transition. Assemblage B can transform into C by initial progress of Ky+Ilm+Chl+Grt+Ms=And+St+Bt+Pl followed by 0.142 Ilm+0.175 St+1.089 Chl+1.533 Ms+0.003 Grt=5.000 And+1.266 Bt+0.551 Pl Matrix analysis cannot satisfactorily model the C–D transition, because it predicts a net production of staurolite, which is in disagreement with petrographic evidence. All mass balances in the C–D composite matrix indicate net consumption of muscovite; this is integrated with the contrasting evidence of prograde pseudomorphs of muscovite after staurolite, observed in the nodules of sample D, within a model involving the progress of ionic reaction cycles.     

碱煮法:一种制备海洋浮游生物PCR模板DNA的实用方法

介绍了一种制备海洋浮游生物PCR模板DNA的方法——碱煮法。取少量海水样品(40μL)．直接经0．25mol／L艺机NaOH和99℃温育处理裂解细胞,从而得到环境样品总DNA。实验证明,该方法制备的模板DNA可用于细菌核糖体RNA、浮游植物叶绿体rbcL和浮游动物线粒体COI等基因的PCR扩增。但是,在使用通用引物扩增细菌基因时,假阳性很难避免。该法制备的模板DNA适用于扩增非细菌基因或者特异引物界定的细菌基因。该方法较传统制备方法快速、简便,样品需要量减少,适用于浮游生物分子遗传多样性研究。     

Melt migration and melt-rock reaction in the Alpine-Apennine peridotites:Insights on mantle dynamics in extending lithosphere

The compositional variability of the lithospheric mantle at extensional settings is largely caused by the reactive percolation of uprising melts in the thermal boundary layer and in lithospheric environments.The Alpine-Apennine(A-A)ophiolites are predominantly constituted by mantle peridotites and are widely thought to represent analogs of the oceanic lithosphere formed at ocean/continent transition and slow-to ultraslow-spreading settings.Structural and geochemical studies on the A-A mantle peridotites have revealed that they preserve significant compositional and isotopic heterogeneity at variable scale,reflecting a long-lived multi-stage melt migration,intrusion and melt-rock interaction history,occurred at different lithospheric depths during progressive uplift.The A-A mantle peridotites thus constitute a unique window on mantle dynamics and lithosphere-asthenosphere interactions in very slow spreading environments.In this work,we review field,microstructural and chemical-isotopic evidence on the major stages of melt percolation and melt-rock interaction recorded by the A-A peridotites and discuss their consequences in creating chemical-isotopic heterogeneities at variable scales and enhancing weakening and deformation of the extending mantle.Focus will be on three most important stages:(i)old(pre-Jurassic)pyroxenite emplacement,and the significant isotopic modification induced in the host mantle by pyroxenite-derived melts,(ii)melt-peridotite interactions during Jurassic mantle exhumation,i.e.the open-system reactive porous flow at spinel facies depths causing bulk depletion(origin of reactive harzburgites and dunites),and the shallower melt impregnation which originated plagioclase-rich peridotites and an overall mantle refertilization.We infer that migrating melts largely originated as shallow,variably depleted,melt fractions,and acquired Si-rich composition by reactive dissolution of mantle pyroxenes during upward migration.Such melt-rock reaction processes share significant similarities with those documented in modern oceanic peridotites from slow-to ultraslow-spreading environments and track the progressive exhumation of large mantle sectors at shallow depths in oceanic settings where a thicker thermal boundary layer exists,as a consequence of slow-spreading rate.     

现代地球化学的理论思维结构

地球科学和地球化学的进展,不但加深和扩大了对地球的认识和理论成果,同时也总结提炼出了全新的科学思维方法。复杂性理论和系统思维是科学认识论的一次飞跃。现代地球化学建立了较完整的理论和方法体系,给地质科学认知地球提供了依据和支撑。作者论证了系统思维和逻辑演绎法相结合的思维方式,是研究和认识地球复杂巨系统以及推动地球科学理论创新的指导思想,并提出了运用现代地球化学理论构架和方法体系,综合地球科学系统思维与逻辑思维相结合方向的地球化学认知模型,为深入研究地球物质能量系统的行为和解决人类面临的资源、环境和灾害问题提供新的思路。     

分层流体中细长体波浪力的数值计算

利用边界元法计算了层化流体中细长体受到的一阶垂荡波浪力和一阶纵摇波浪力矩，计算了近水面细长体的波浪力及力矩，与水池实验结果相吻合。     

泡沫镍基P-25薄膜光催化降解水中喹啉

为了提高TiO²薄膜的光催化效率和使用稳定性,采用浸渍涂布法将粉体P-25 TiO₂负载在泡沫镍基片上,制备泡沫镍基负载P-25薄膜光催化材料,利用XPS和FE-SEM分析了薄膜的晶相和形貌,并考察了不同条件下P-25薄膜对水中喹啉的降解效能。研究发现：P-25薄膜均匀覆盖泡沫镍基片表面,薄膜呈混晶结构,表面呈现微裂痕。实验表明：增大光照强度和曝气量能够明显提高水中喹啉的光催化降解率;低pH有利于水中喹啉的去除;初始浓度和温度不是光催化反应的主控因子;曝气产生的吹脱、扰动和水力紊流效应对光催化反应的影响不明显。结果显示：不改变水溶液温度和pH条件下,P-25薄膜对水中喹啉有良好的去除效果,并可多次重复使用。     

层状复合氢氧化物对硫酸钠的阴离子交换作用

以0.004~0.80 mol.L-1的Na2SO4溶液为交换介质,测定了层状复合氢氧化物(LDH)[Mg4.7Al(OH)11.4]Cl0.96(OH)0.04.7.9H2O在超声条件下的离子交换容量和交换平衡常数。结果显示层间Cl-离子的最大交换容量为1.497 mmol.g-1,OH-离子的最大交换容量为0.026 8 mmol.g-1,交换平衡常数pK值为3.65;固相的XRD、IR及BET-N2表征显示交换反应后SO42-的Td对称性降低,LDH的晶胞参数c和通道高度h增大,结晶度下降,微晶的层间吸附活性降低,微孔吸附容量减小。     

中国北方晚中生代陆相盆地红-黑岩系耦合产出对砂岩型铀矿成矿环境的制约

为研究中国北方陆相盆地红层-黑色岩系对砂岩型铀成矿的制约,文章研究了国内外红-黑岩系与砂岩型铀矿赋存岩层的时空关系,筛选了10万余m岩心钻探资料,选择准噶尔、鄂尔多斯和松辽盆地这3个典型产铀盆地,通过编制盆地钻孔柱状图、典型地区连井剖面图及关键岩层的地球化学测试等方法,对红-黑岩系和砂岩型铀矿的赋存岩层进行了垂向、横向上综合分析与对比。研究发现:北方陆相盆地自西向东铀矿赋存地层的时代由中侏罗世过渡到晚白垩世;晚中生代至少存在6次大规模的富氧红层沉积事件:Ⅰ中侏罗世—晚侏罗世早期(BathonianOxfordian),Ⅱ早白垩世早中期(Berriasian-Barremian),Ⅲ早白垩世中期(Barremian),Ⅳ晚白垩世早期(Cenomanian),Ⅴ晚白垩世中期(Coniacian)和Ⅵ晚白垩世晚期(Campanian)。其中第Ⅰ、Ⅴ和Ⅵ期红层之下沉积了时代相近的黑色层,与之构成"红-黑岩系"的沉积结构,是北方砂岩型铀成矿的3个重要层位。典型盆地内地球化学表明,红层与黑色层的B、Sr和Cu元素含量及Fe~(2+)/Fe~(3+)、B/Ga、Sr/Cu和FeO/MnO比值具有明显的差异,结合黑色岩层中草莓状黄铁矿、碳屑、油斑和红层中碳酸盐岩的发育,认为红层为相对较强氧化环境,黑色层为相对较还原环境。连井剖面资料显示红层、黑色层与砂岩型铀矿空间关系密切,铀矿多产于红层与黑色层之间过渡带上,呈板状矿体赋存于灰色、绿灰色砂岩和细砂岩中。一般红层与黑色层垂向距离超过500 m不利于成矿。晚中生代陆相盆地内耦合产出的黑色岩系和红色岩系是古沉积环境由还原向氧化转变形成的垂向分带,前者为铀矿物质沉淀提供了"障",后者为表生流体溶解铀矿提供了"场"。文章初步提出了红-黑岩系垂向环境变化制约着北方陆相盆地砂岩型铀大规模成矿作用的新认识。这些认识不仅对砂岩型铀矿成矿环境、成矿规律及成矿模式研究具有重要意义,更对目前正在开展的砂岩型铀矿勘查工作具有实践指导意义。