Degradation of Tetrachloroethene by Several Co-metabolism Substrates in Groundwater

Tetrachloroethene （PCE） is biodegraded by reductive dechlorination with co-metabolism substrates under anaerobic conditions. By inoculating sludge from an anaerobic pool, a biodegradation test of PCE is conducted in the anaerobic condition. In the test, several substrates including methanol, ethanol, formate, acetate, lactate and glucose, are conducive to the conversion from PCE to TCE and 1,1-DCE. The results show the microbe can be cultivated well under the anaerobic circumstances of mixture of sewage （sludge） and soil with the index of COD after eleven days. Degradation of PCE accords with one order reaction kinetics equation. The sequence of the reaction rate constant is Kacetate 〉Kglucose 〉 Klactate 〉 Kethanol 〉 Kformate 〉 Kmethanol, and acetate is an outstanding co-metabolism substratum whose reaction rate constant is 0.6632d^-1.     

东帝汶海MD98-2172岩芯磁记录与还原成岩作用过程

MD98-2172岩芯位于印度尼西亚穿越流的帝汶通道上.多参数的岩石磁学测量结果表明,该岩芯的磁性矿物组合很好地记录了海洋沉积物中的还原成岩作用过程:0～3.85 m段岩芯以亚铁磁性准单畴(PSD)磁铁矿为主,其含量和粒度基本不随深度而变,受还原成岩作用的影响不明显;3.85～5.35 m段岩芯也以PSD磁铁矿为主,但其含量随深度的增加而快速减少,粒度随深度的增加而变粗,或粗粒磁铁矿的相对含量随深度的增加而增多,处于铁氧化物还原阶段;5.35～15.00 m层段以顺磁性颗粒为主,并出现黄铁矿,处于硫酸盐还原阶段.     

水资源中氯代烃污染物的去除方法

随着工业化的发展。氯代有机溶剂使用越来越广泛。并且难于去除。在20世纪90年代初期，人们就已认识到用Fe^0恢复污染的地下水的潜力。国外正在研究帮使用扔几种还原挥发性氯代烃的还原反应介质，尤其要提高的是双金属反应系统，反应速度快，而且脱Cl中国难解产物少，目前国也只停留在实验室研究阶段，个别做了地上反应器的验证实验，它的脱Cl机理、介质钝化和完全脱Cl问题还有待于进一步研究。     

Magnetic properties of recent sediments in Lake Baikal, Siberia

Mineral magnetic measurements of six ²¹⁰Pb-dated surface cores from different basins of Lake Baikal, Siberia, show temporal records controlled by a range of internal and external processes. With the exception of sediments on the Academician Ridge, there is clear evidence for widespread reductive diagenesis effects on the ferrimagnetic component coupled with neo-formation of paramagnetic iron minerals. Greigite formation, bacterial magnetosome accumulation and turbidite layers may affect the properties of some sediment levels. Concentrations of canted antiferromagnetic minerals (eg. haematite) appear to increase from the 19th century onwards. These minerals are less affected by dissolution processes and probably represent detrital minerals delivered by catchment fluvial processes. The magnetic evidence for recent atmospheric pollution by fossil-fuel combustion processes is weak in all the cores, and supports the findings from studies of spherical carbonaceous particles (SCPs) and heavy metals that pollution is largely restricted to the southern basin. Correlations between recent sediments based on magnetic data may be insecure over long distances or between basins.     

Fe(Ⅱ)/针铁矿复合系统对水中橙黄G的吸附-还原脱色研究

系统研究了Fe(Ⅱ)/针铁矿复合系统对偶氮染料橙黄G(简称OG)的吸附-还原脱色机理,重点考察了反应条件p H值、Fe(Ⅱ)与OG摩尔比对OG还原脱色效果的影响。研究结果表明,矿物表面结合态Fe(Ⅱ)能够有效提高还原脱色反应速率;OG脱色反应非常符合准一级反应动力学方程,速率常数(k)随p H值的升高、亚铁离子吸附量的增加而显著增大;当OG初始浓度为50 mg/L、Fe(Ⅱ)与OG的摩尔比为27.0时,Fe(Ⅱ)/针铁矿复合系统对OG的去除脱色率在弱碱性条件下1 h内可达到100%。该系统对OG去除脱色的高效性是界面吸附与还原协同作用的结果。该研究可为有效应用Fe(Ⅱ)/针铁矿复合系统在缺氧环境中的污染修复提供理论指导。     

山西省落家河铜矿地质特征及矿床成因浅析

落家河矿田位于中条三叉裂谷南东支的落家河构造剥蚀天窗内,该区域位于线性构造和弧形构造的交叉部位,是成矿有利部位.落家河矿区赋矿岩性为新太古界绛县群宋家山组绿泥片岩和变细碧岩.宋家山组一套钠质中基—中酸性火山凝灰岩夹正常沉积钙质副变质岩组成.经变质后的绿片岩层是主要找矿层位,特别是该岩层沿走向或倾向变化大和膨胀部位.硅化...     

土著微生物作用下含水层沉积物砷的释放与转化

在原位采集内蒙古河套平原高砷含水层中沉积物和土著微生物的基础上,进行了室内微生物淋滤实验研究。实验过程中,使用了3种水溶液(包括去离子水和2种人工配水)和2种营养条件(包括添加2%葡萄糖和未添加葡萄糖)。结果表明,葡萄糖可强化土著微生物的活性,使得悬浮液pH值明显降低,并增加悬浮液中As质量浓度。配水成分影响悬浮物中As质量浓度。在第9 d之后,添加葡萄糖的样品中存在一定强度的硫酸根还原作用,且这种脱硫酸作用受配水成分的影响较小。研究表明,土著微生物影响下砷的释放和转化过程包括沉积物中As(V)的释放、溶液中As(V)的还原以及沉积物中As(Ⅲ)的释放等。与溶液As(V)相比,As(Ⅲ)更有利于沉积物As的释放。在As释放的过程中,溶液中Fe/Mn含量同时增加,且呈很好的线性相关关系。这意味着土著微生物作用下Fe/Mn氧化物矿物的还原性溶解是导致沉积物As释放的主要原因之一。     

磁性矿物还原成岩作用述评

许多海洋－湖泊环境中的沉积物受到还原成岩作用的影响发生磁性颗粒的溶解和自生现象。根据最近二十多年的研究成果,简要介绍了磁性矿物发生还原作用的基本过程、产物和控制因素,成岩作用对沉积物地球化学和磁学特征的改变,成岩自生亚铁磁性铁硫化物的磁学特征以及成岩作用对古地磁和环境磁学记录的影响。     

纳米镍/铁去除氯代烃影响因素的探讨

氯代烃是地下水中最常检出的有机污染物之一,传统的处理方法去除率很低。近年来随着铁还原技术的发展,纳米铁和纳米双金属也成为一个活跃的研究领域。利用批实验的研究方法以四氯乙烯(PCE)和四氯化碳(CT)为目标污染物,研究纳米镍/铁在去除PCE过程中的影响因素。实验结果表明,在碱性条件下,纳米Ni/Fe对PCE脱氯速率比在酸性和中性条件下脱氯速率更快;纳米Ni/Fe对初始浓度为6·51mg/L的PCE溶液脱氯速率是对初始浓度为20·56mg/L的PCE溶液脱氯速率的1·8倍;对于氯代程度相同的CT和PCE,对CT的脱氯速率明显快于对PCE。     

Dechlorination of trichloroethylene in solution over supported nano zero valent Fe and Cu/Fe bimetal on exfoliated graphite

Degradation of organic halides by reductive dehalogenation promoted by zerovalent metals is a very active research area. The use of nano-sized particles of zero valent iron （ZVI） or bimetallic combinations of ZVI currently attracts the most attention due to their high surface areas and high reactive activity. The introduction of second catalytic metals, such as Pd, Pt, Cu, or Ni, results in an even higher dehalogenation rate. The supported zero-valent iron materials have higher activity and greater flexibility for environmental remediation applications than other forms of ZVI. Nano ZVI supported on micro-scale exfoliated graphite was prepared by using KBH4 as the reducing agent in the H2O/ethanol solution of Fe^2＋ in the laboratory. Then the ethanol solution of Cu^2＋ was added to the fleshly prepared wet supported nano ZVI. The Fe/Cu bimetallic particles supported on the graphite were obtained because of the reduction and deposition of Cu on the Fe surface. The TEM image showed that iron particles were highly dispersed on the surface of graphite. In this study, supported zero valent Cu/Fe bimetallic nanoparticles were used for the dehalogenation of trichloroethylene （TCE） in batch experiments. The dechlorination rate of supported zero valent Fe/Cu bimetallic nanoparticles was greater than the supported nano ZVI. Supported Cu/Fe bimetal with 4 wt% Cu had the fastest dehalogenation rate than that with different content of Cu. When the nana FeO dosage was 5 g/L in the dehalogention system, 8 mg/L of TCE was completely dechlorinated within 4 hours. Increasing or decreasing the FeO dosage, the dechlorination rate could be worse. When the concentration of Fe^2＋ was 0.05 mol/L during the preparation by KBH4 reduction, the nano Cu/Fe particles exhibited the spheral shape with 50-80 nm in size. When the concentration of Fe^2＋ was higher （0.2 mol/L）, the nano particles were the palpus structure and had the poor dehalogenation effect on the TCE.