岩矿显微组构对水银洞金矿成因的指示

黔西南水银洞金矿为产于上二叠统龙潭组中的超大型、高品位金矿床,矿床由多个金矿体组成.工业金矿体顺层产于龙潭组含煤地层所夹的玄武质、硅质、生物碎屑碳酸盐岩中.对水银洞金矿赋矿地层岩石以及矿石显微组构进行了研究,矿石中主要载金矿物为细粒黄铁矿,具再生边、粒内孔隙、铸模孔隙结构及镶边生物矿化构造、铸模式生物矿化构造,是一典型的具沉积一成岩组构.金矿化与硅化有密切的成因联系,金与SiO2来源于峨嵋山玄武岩的喷溢活动,主要金矿体更多显示与峨嵋山玄武岩准同生特征.矿床为沉积一成岩弱改造成囚金矿床.     

SO4^2-改性铁铝复合层柱粘土的制备及其催化性能研究

由共聚法制得的铁铝复合交联剂交换钠基蒙脱石层间的水合钠离子,再经SO42-改性处理制备了铁铝复合层柱粘土固体超强酸催化剂.利用xRD、FT-IR和BET法对催化剂的结构进行了表征.以乙酸正丁酯的合成反应为探针反应对催化剂的活性进行了测试.通过正交实验确定了铁铝复合交联粘土SO42-改性最佳工艺条件.研究了催化剂对探针反应的选择性及重复使用情况.结果表明:在由实验确定的最佳改性工艺条件下,乙酸的转化率达92.2%,反应中无副产物产生,催化剂具有较好的重复使用性能.     

湖北徐家山锑矿床铅同位素组成与成矿物质来源探讨

徐家山锑矿床位于湖北省通山县境内,矿体赋存于上震旦统灯影组和陡山沱组地层中.对采自该矿的辉锑矿进行了系统的铅同位素测定.结果表明,在徐家山矿区范围内存在两组明显不同的铅同位素组成:A组206Pb/204Pb为18.874～19.288,207Pb/204Pb为 15.708～15.805, 208Pb/204Pb为38.642～39.001, 为高放射性成因铅;B组以低放射性成因铅为特征,其同位素组成206Pb/204Pb为17.882～18.171,207Pb/204Pb为15.555～15.686,208Pb/204Pb为37.950～38.340.对应地,相关参数也明显不同,如单阶段模式年龄,A组为负值或极小的正值,而B组为636～392 Ma.铅同位素组成与某些相关参数(Δγ与Δβ、V1与V2)之间呈明显线性正相关关系.根据铅构造模式和矿石铅同位素的Δγ-Δβ成因分类图解等综合分析,A组辉锑矿的铅主要来源于赋矿围岩--震旦系海相碳酸盐岩,B组主要来源于赋矿围岩的下伏基底碎屑岩--中元古界冷家溪群浅变质岩系.研究结果不支持前人沉积-改造成因的观点,成矿物质是多来源的,部分成矿物质来自基底地层.     

贵州省册亨县百地金矿地质特征及找矿前景

将册亨县百地金矿矿区划分为3个矿段,并简要描述各矿段(体)地质特征及取得的勘查进展情况。初步预测各矿体找矿前景及资源潜力。     

贵州晴隆大厂晚二叠世初期河流相沉积特征——兼论与上下地层接触关系

晚二叠世初期,在晴隆大厂一带,以"大厂层"为基底的山间盆地中,形成了一条自北东流向南西的规模较大的曲流河。该河流微相发育,其沉积物包括河道砾岩、边滩砂屑岩和洪泛平原泥质岩等。这套沉积地层上与上二叠统峨眉山玄武岩下与"大厂层"或局部与中二叠统茅口组接触。此乃峨眉地幔隆起边缘的沉积效应。     

中国开辟区不利开采地形类型及其分布

利用1998年"大洋一号"调查船近海底作业所获的深拖海底电视和照相系统资料,对中国开辟区不利开采地形类型及其分布特征进行了研究,并对海底地形的坡度进行了计算,结果表明:(1)中国开辟区东、西两区海底的东向坡和西向坡是均衡分布的。东、西两区海底地形坡度的分布特征明显不同,东区海底地形坡度以0～15°为主,而西区坡度大于3°的地形则很少。坡度大于5°的地形主要分布于坡脚处,特别是坡度超过15°的地形总是出现在水深变化的转折点处。(2)研究区不利开采地形可分为坡度为5～15°和大于15°两种类型,东区地形坡度大于5°的不利开采地形比西区多14%,东区坡度大于15°的地形为3.6%,比西区(仅为1.4%)多,东、西两区都有少量坡度近90°的地形出现,并且这种地形在东区所占比率比西区大,说明东区断崖、陡坎和断裂沟槽比西区多,地形也更为复杂多变。     

南海尖峰海山多金属结壳地球化学

南海尖峰海山多金属结壳富含30多种元素,其锰铁矿物主要由钡镁锰矿,δ-MnO_2和FeOOH·xH_2O组成。与其它海区的结壳相比,尖峰海山结壳富含Cu、Ni、Ba、Zn、Pb等元素,而Co、Ti、稀土元素(REE)、Sr等元素相对较贫。研究表明,HREE亏损,具明显的Ce正异常,较明显的Tb正异常和Yb负异常。这是氧化弱碱性海洋环境所致。结壳是水成作用的产物,它的形成受南海独特的古海洋环境所控制,海底火山热液作用,可能也是影响因素之一。     

地形坡度对多金属结核分布的控制作用

选取我国东太平洋多金属结核开辟区内的一个区域作为研究区,利用人工神经网络中应用最为广泛的BP网络,建立控制多金属结核分布的地质因素与多金属结核分布之间的映射关系,探讨地形坡度对多金属结核分布的控制作用.结果表明,在经度、纬度、水深、坡度四个因素中,坡度对结核分布影响程度最大;多金属结核主要分布于坡度小于5°的地方;当坡度小于5°时,丰度与地形坡度呈正相关,品位与地形坡度呈负相关,丰度与品位呈负相关;品位与坡度似呈指数关系,坡度增大,品位降低.     

On the relevance of iron adsorption to container materials in small-volume experiments on iron marine chemistry: Fe-aided assessment of capacity, affinity and kinetics

Iron chemistry in seawater has been extensively studied in the laboratory, mostly in small-volume sample bottles. However, little has been reported about iron wall sorption in these bottles. In this paper, radio-iron ⁵⁵Fe was used to assess iron wall adsorption, both in terms of capacity, affinity and kinetics. Various bottle materials were tested. Iron sorption increased from polyethylene/polycarbonate to polymethylmetacrylate (PMMA)/high-density polyethylene/polytetrafluoroethylene to glass/quartz, reaching equilibrium in a 25–70 h period. PMMA was studied in more detail: ferric iron (Fe(III)) adsorbed on the walls of the bottles, whereas ferrous iron (Fe(II)) did not. Considering that in seawater the inorganic iron pool mostly consists of ferric iron, the wall will be a factor that needs to be considered in bottle experiments.The present data indicate that for PMMA with specific surface (S)-to-volume (V) ratio S/V, both iron capacity (42 ± 16 × 10^− 9 mol/m² or 1.7 × 10^− 9 mol/L recalculated for the S/V-specific PMMA bottles used) and affinity (log K_Fe'W = 11.0 ± 0.3 m²/mol or 12.4 ± 0.3 L/mol, recalculated for the S/V-specific PMMA bottles used) are of similar magnitude as the iron capacity and -affinity of the natural ligands in the presently used seawater and thus cannot be ignored.Calculation of rate constants for association and dissociation of both Fe'L (iron bound to natural occurring organic ligands) and Fe'W (iron adsorbed on the wall of vessels) suggests that the two iron complexes are also of rather similar kinetics, with rate constants for dissociation in the order of 10 ⁻⁴–10^− 5 L/s and rate constants for association in the order of 10⁸ L/(mol s). This makes that iron wall sorption should be seriously considered in small-volume experiments, both in assessments of shorter-term dynamics and in end-point observations in equilibrium conditions. Therefore, the present data strongly advocate making use of iron mass balances throughout in experiments in smaller volume set-ups on marine iron (bio) chemistry.