Kinetics of phosphate adsorption by iron oxyhydroxides in aqueous systems

The rate of uptake of phosphate onto synthetic Fe(III)- and Fe(II)-derived oxyhydroxides has been studied using reaction conditions similar to those encountered in natural waters. Kinetic analyses were carried out on the adsorption profiles and both first-order and second-order conditional rate constants were obtained. The temperature dependence of some of the rate constants was investigated and corresponding apparent activation energies calculated. Similar experiments and analyses were undertaken using Fe from natural sources and in general the conditional rate constants obtained in seawater were in agreement with the synthetic ones. The results of this study are of value when comparing the time scales of adsorption processes in natural waters with the time scales of mixing and advection.     

Estimation of Fe3+ from electron microprobe analyses: observations on calcic amphibole and chlorite

ABSTRACT Metabasites and metagreywackes from the Pelona and Rand Schists of southern California were analysed using three different electron microprobes. For all three instruments, the estimated Fe³⁺ contents of calcic amphibole, chlorite and epidote are positively correlated. For some samples, there is an additional correlation between high estimated Fe³⁺ and the presence of magnetite. These results imply that microprobe analyses can be used to discern relative differences in Fe³⁺. However, microprobe data and calculations on the sensitivity of the correction procedures to systematic analytical errors indicate that estimated values of Fe³⁺ are not significant in an absolute sense. Thus, estimates of Fe³⁺ are meaningful when comparing samples analysed with a single microprobe, but must be used with caution when comparing analyses obtained on more than one probe.     

Behaviour of iron,manganese, phosphate and humic acid during mixing in a Delaware salt marsh creek

The mixing behaviour of iron, manganese, phosphate and humic acid in a Delaware salt marsh creek was studied using field data, laboratory mixing experiments, and geochemical mass balance equations. Property-salinity diagrams for field data indicated that the removal of iron is 56–70% in the 0–10‰ salinity range. A proposed mechanism of removal is the flocculation of colloidal iron, perhaps with humic acid. Phosphate, however, undergoes 195% addition in the same low salinity region, which may be due to release of phosphate from resuspended sediments. Dissolved manganese is conserved, as is humic acid throughout the salt marsh mixing zone. Within the uncertainty of the data the maximum possible removal of humic acid is 23%.Laboratory mixing experiments that simulated salt marsh mixing along the same salinity gradient as observed in the field (5–25‰) showed only small-scale additions and removals compared to the field results. Such small-scale changes occurred largely at salinities >10‰ in the laboratory experiments, whereas most removals and additions occurred at salinities <10‰ in the field. Mixing studies also showed little difference between prefiltered and unfiltered mixes. The studies suggest that simple mixing of salt marsh waters, with or without suspended material, does not strongly influence the observed behaviour of dissolved constituents in salt marshes, and that other processes (e.g. sediment or intertidal exchange) must dominate their behaviour.     

不同沉淀法处理含铬废水的比较

含铬废水具有有机物含量高,难降解物质浓度高,色度大,悬浮物多,水质、水量变化大,含有微量毒性物质等特点。本文探讨了在不同参数条件下,硫酸亚铁、铁、硫化亚铁三种还原剂对含铬废水处理效果的影响,实验表明:硫酸亚铁具有明显的优越性,在同等条件下其去除率达到99%以上。     

冀南邯邢地区白涧和西石门夕卡岩型铁矿磁铁矿成因矿物学研究

对邯邢地区典型夕卡岩型铁矿床白涧铁矿和西石门铁矿中不同产状的磁铁矿的成分、热电性、爆裂温度及O同位素进行了详细的成因矿物学研究。研究发现：层间矿体具有低Ti、∑REE、爆裂温度、δ18O的特征,热电性系数较小但变化范围大;接触带矿体为高Ti、∑REE、爆裂温度、δ18O的特征,热电性系数较大,变化范围小。白涧铁矿层间矿和西石门铁矿中磁铁矿的REE表现出Eu的正异常,而白涧铁矿接触带矿为负异常。白涧铁矿磁铁矿中单层矿体热电性系数具有中部小、顶底大的特征。综合磁铁矿的成因矿物学研究,以热电性的空间变化规律为基础,建立了该区夕卡岩型铁矿的成因和找矿模型。     

岩石直接剪切试验残余强度浅析

对岩石剪切残余强度进行了浅析,主要以唐山马城铁矿的岩石试验为依据,探讨了岩石剪切峰值强度和残余强度的关系,分析了岩石剪切残余强度的影响因素,为大家了解、利用岩石的剪切残余强度提供了参考意义。     

新疆磁海铁（钴）矿床次火山热液成矿学

磁海铁（钴）矿床颇具特色,以“石榴石－透辉石－磁铁矿”为基本矿石建造;成矿作用发生在早二叠世北山裂陷作用和火成活动晚期,以基性次火山岩浆期后富铁流体的（交代）充填为成矿方式,矿体产于辉绿岩体原生裂隙系统;成矿流体的化学演化具有典型（火山）岩浆期后热深演化特点,形成了一系列热液蚀变其中石榴石透辉石岩有别于传统理解的“夕卡岩”;成矿物质源于碱性玄武岩浆,基性次火山岩浆多次脉动式入侵是矿床形成的必要条件     

航磁梯度数据解释新方法在迁安铁矿勘探中的应用

为更加清晰和准确地利用磁梯度数据获得地质体的分布特征,笔者采用解析信号总水平导数法和梯度欧拉反褶积技术组合实现磁梯度数据的解释,解析信号总水平导数的极值可有效地圈定出矿体的分布范围,梯度欧拉反褶积法可有效地避免背景异常的干扰,从而准确地给出磁性体的位置和深度信息。理论模型证明解析信号水平导数法和梯度欧拉反褶积法的组合可准确地获得磁性体的水平范围和深度。应用于河北迁安地区磁梯度数据的解释,圈定出5个呈条带状分布的较大型铁矿藏,埋深在200~450 m。     

硫酸盐还原菌及异化铁还原菌对 黄钾铁矾还原作用的对比

选取酸性矿坑水环境中常见的次生含铁硫酸盐矿物———黄钾铁矾[KFe3(SO4)2(OH)6]为研究对象,用硫酸盐还原菌 Desulfovibriovulgaris 和异化铁还原菌Shewanellaputrefaciens CN32对其进行还原实验,探讨作为重金属治理潜在材料的 黄钾铁矾的微生物稳定性.实验采用非增长型培养基,在中性、厌氧、30℃的条件下进行.采用湿化学方法测量水溶液及还原产 生的总Fe2+ ,利用X射线衍射(X-raydiffraction,简称XRD)来分析反应后残余固体物质的矿物组成,用扫描电镜(scanning electronicmicroscopy,简称SEM)观察固体残余物的形貌特征.结果表明,没有微生物的参与,黄钾铁矾的稳定性较好.异化铁 还原菌S.putrefaciens CN32和硫酸还原菌D .vulgaris 在营养极其匮乏的中性厌氧条件下均能还原黄钾铁矾晶格中的 Fe3+ ,显示出黄钾铁矾被微生物还原的可能性.S.putrefaciens CN32还原黄钾铁矾晶格中Fe3+ 的最大还原速率和最终Fe3+ 还原率分别为0.001mmol·L-1·h-1和0.37%.与S.putrefaciens CN32不同,D .vulgaris 对黄钾铁矾的还原能力较强,不 含有电子穿梭体(Anthraquinone-2,6-disulfonate,简称AQDS)的实验体系中Fe3+ 的最大还原速率和最终Fe3+ 还原率分别为 0.017mmol·L-1·h-1和16.80%,而添加了AQDS的实验体系的则分别达到了0.026mmol·L-1·h-1和24.30%,这可能与 黄钾铁矾中含有SO42- 有关.D .vulgaris 优先还原黄钾铁矾晶格中的SO42- 产生的H2S是强还原剂,也可促进Fe3+ 的还原, 微生物以及H2S的双重作用可能是导致D .vulgaris 体系中Fe3+ 还原率较高的原因.XRD分析表明,黄钾铁矾经过S.putrefaciens CN32的作用,物相没有发生变化;而经过D .vulgaris 作用后,黄钾铁矾的特征峰消失,固相残余物中出现了菱铁 矿(FeCO3)、蓝铁矿[Fe3(PO4)2·8H2O]等次生矿物.由于培养基中没有添加任何的磷酸盐,因此蓝铁矿的出现可能是由于培 养基中添加的少量酵母浸膏降解后产生的磷酸根与D .vulgaris 还原黄钾铁矾产生的Fe2+ 相互作用的结果.这些认识对深入 理解地球表层铁的生物地球化学循环具有重要意义,为矿山环境重金属的污染治理提供了实验依据.