水稻根表铁膜对水稻根吸收铅的影响

采用土-砂联合培养方法诱导水稻根表形成不同数量的铁膜:高铁膜(HP)和低铁膜(LP),探讨铁膜形成的多少对水稻离体根系吸收铅的影响.结果表明,在水稻生长期间,水分显著影响根表形成铁膜的数量.水稻吸收的铅大部分结合在根组织中(平均75%),少部分富集在根表铁膜中(平均25%).与低铁膜相比,高铁膜可以增强铅在水稻根表铁膜和根中的积累,由此可见,铁膜可能在一定程度上促进铅向水稻根内的转运.     

义乌市TSP中3种重金属元素的沉降

测定了义乌市TSP及其中的重金属Fe,Mn和Cu的浓度,通过扫描电镜和降雨冲洗效果分析了含有这3种重金属的颗粒物的粒径,计算了3种重金属的沉降通量。结果表明相对于世界其他城市,义乌市TSP中这3种重金属浓度偏高;绝大部分TSP的半径小于4.5μm;Fe和Mn的湿沉降量大于干沉降量,而Cu以干沉降为主。     

Ni/Fe双金属降解四氯化碳和四氯乙烯的对比试验

以四氯化碳(CT)和四氯乙烯(PCE)为目标污染物,以批试验方法研究Ni/Fe双金属对CT和PCE的还原性脱氯.结果表明:Ni/Fe双金属可有效去除水中的CT和PCE;Ni/Fe双金属对CT和PCE的降解反应均符合准一级反应动力学方程;在相似的反应条件下,Ni/Fe双金属对CT和PCE脱氯的反应速率常数(kobs)之比为1.48和1.67,说明Ni/Fe双金属对CT的脱氯速率要快于对PCE的脱氯速率;Ni/Fe双金属可对PCE完全脱氯,但对CT脱氯过程中产生少量三氯甲烷(TCM).     

含铁化合物对有机氯化物的脱氯处理技术研究

综述了钯 /铁、二硫化铁、硫化铁、三氧化二铁、绿锈等含铁化合物在降解六氯乙烷、四氯化碳、五氯乙烷、四氯乙烷、三氯乙烷、三氯乙烯、四氯乙烯等有机氯化物中的应用以及降解机理     

Dssimilatory Fe(Ⅲ) reduction characteristics of paddy soil extract cultures treated with glucose or fatty acids

Dissimilatory Fe(Ⅲ) reduction is a universal process with irreplaceable biological and environmental importance in anoxic environments. Our knowledge about Fe(Ⅲ) reduction predominantly comes from pure cultures of dissimilatory Fe(Ⅲ) reducing bacteria (DFRB). The objective of this study was to compare the effects of glucose and a selection of short organic acids (citrate, succinate, pyruvate, propionate, acetate, and formate) on Fe(Ⅲ) reduction via the anaerobic culture of three paddy soil solutions with Fe(OH)3 as the sole electron acceptor. The results showed significant differences in Fe(Ⅲ) reduction among the three paddy soil solutions and suhstrate types. Bacteria from the Sichuan paddy soil responded quickly to substrate supply and showed higher Fe(Ⅲ) reducing activity than the other two soil types. Bacteria in the Jiangxi paddy soil culture solution could not use propionate as a source of electrons for Fe(Ⅲ) reduction. Similarly, bacteria in the Jilin paddy soil culture could not use succinate effectively. Pyruvate was readily used by cultures from all three paddy soil solutions, thus indicating that there were some similarities in substrate utilization by bacteria for Fe(Ⅲ) reduction. The use of glucose and citrate as substrate for dissimilatory Fe(Ⅲ) reduction indicates important ecological implications for this type of anoxic respiration.     

地下水中铁、锰的存在形式及去除技术探讨

地下水中铁、锰存在形式复杂 ,铁锰超标产生一定的危害性 ,本文通过研究地下水除铁除锰技术的发展趋势 ,对现有除铁除锰技术进行比较 ,阐明了生物除铁除锰技术的发展前景     

A three-dimensional model for the transportation of Fe and Mn in Arha Reservoir

ＩｎｔｒｏｄｕｃｔｉｏｎＡｒｈａＲｅｓｅｒｖｏｉｒｉｓｌｏｃａｔｅｄｉｎｔｈｅｐｌａｔｅａｕｒｅｇｉｏｎｏｆＳｏｕｔｈｗｅｓｔＣｈｉｎａ.Ｔｈｉｓｒｅｓｅｒｖｏｉｒ,ｗｉｔｈａｖｏｌｕｍｅｏｆ445ｍｉｌｌｉｏｎｍ3,ｗａｓｂｕｉｌｔｉｎ1960ａｎｄｉｓｔｈ?..     

环境水样中痕量Fe3+的测定方法研究

在酸性介质中(pH 5.0),Fe3+能与硫氰酸盐生成稳定的配离子[Fe(SCN)6]3-,该配阴离子能与碱性717型阴离子交换树脂定量交换缔合,形成阴离子交换树脂(R+)--金属离子(Mn+)--硫氰酸盐(SCN-)三元配合缔合体系,其最大吸收波长分别为490 μm,与二元水相最大吸收波长相同,通过制作薄层测定了水中Fe3+含量.本法具有较高的灵敏度ε630Fe3+=2.4×105 L·mol-1·cm-1,测定0.6 μgFe3+6次,RSD=2.7%,实测了水样中,Fe3+含量并与AAS法测定结果比较,Fe3+测定的线性范围0～10 μg/25mL,体系检出限为0.12 μmol/L.     

铁(Ⅲ)-羧酸配合物对水溶性染料的光化学脱色动力学的比较研究

铁-柠檬酸，铁-酒石酸，铁-丁二酸，铁-草酸配合物在高压汞灯（λmax＝313nm，250W）的照射下，能使活性艳红X－3B染料水溶液脱色。染料初始浓度在10mg／L～50mg／L时，染料脱色为动力学一级反应，脱色速率随初始浓度增大而降低。在pH2．0～3．0时铁-柠檬酸，铁-滴石酸，铁-丁二酸的染料溶液脱色效果较佳，在pH4．0时铁-草酸的染料溶液脱色效果最好。铁／羧酸盐配比对染料脱色速率也有影响。     

Second german heavy-metal survey by means of mosses,and comparison of the first and second approach in germany and other european countries

This paper shows the geographic distribution in Germany of iron (Fe), nickel (Ni) and lead (Pb) analyzed in mosses in 1995/96 and compares it with the results of the 1990/91 pilot study within a European moss-monitoring programme. Other elements (As, Cd, Cr, Cu, Ti, V, Zn) are compared on basis of the overall element medians for Germany of the 1990/91 and 1995/96 survey. Samples of Pleurozium schreberi, Scleropodium purum, Hypnum cupressiforme and Hylocomium splendens were taken at a total of 1026 sites. In the 1995/96 monitoring campaign, 95% of the original sites of the 1990/91 study were resampled. The results from 1995/96 display local elevated values and many cases of areas affected by known sources of heavy-metal emissions. The industrialized and urban regions of Germany are shown up clearly by the 1995/96 moss-monitoring results: the Ruhr area, parts of Saarland and Baden-Württemberg, as well as areas in eastern Germany. Relatively low values for many elements were found in large areas of Lower Saxony and Bavaria. A comparison of the results of the 1990/91 and 1995/96 moss-monitoring programmes shows a fall in the concentration of the presented elements (except cadmium, copper and zinc) over the relevant period. Especially in the former GDR, chromium (Cr), iron (Fe), titanium (Ti) and vanadium (V) decreased significantly. This is, firstly, a reflection of the closure of and/or technological improvements to large power plants; secondly it is due to the fact that lignite has given way to other fuels. Vanadium (V) and nickel (Ni), typical constituents of crude oil, also show a decrease in the western part and thus document changes in the type of fuel consumed. The significant fall in lead concentration in 1995/96 as compared to 1990/91 in what used to be East and West Germany probably results from the increasing use of lead-free petrol. A comparison of the median values for 1990/91 and 1995/96 in mosses to the rate of emission of heavy metals in Germany for 1990 and 1995 shows similar trends in the case of elements such as arsenic (As), chromium (Cr), nickel (Ni), and lead (Pb). The comparison of the medians of the elements analyzed for 19 European countries indicates for most of the elements a general tendency to lower values in 1995, except for Lithuania, Netherlands, Portugal, Italy and United Kingdom.