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131.
海洋沉积物中还原性无机硫和活性铁的地球化学过程与沉积物环境质量演变密切相关。本研究利用改进的冷扩散法和盐酸萃取法分别对烟台夹河口北部海域深约4 m的柱状沉积物中的酸性可挥发硫(AVS)、黄铁矿硫(CRS)、元素硫(ES)和活性铁(FeⅡ和FeⅢ)进行了测定,并从地球化学机理方面探讨了硫与铁的分布特征及其耦合机制。结果表明,烟台夹河口北部近海深层柱状沉积物中还原性无机硫以CRS为主,其次是AVS和ES,其中AVS含量垂向分布较均匀,而CRS和ES含量在垂向上呈表层和底层高,中间层低的趋势;活性铁以Fe(Ⅱ)为主,其随深度增加而增加,Fe(Ⅲ)随深度逐渐降低,大部分Fe(Ⅲ)被还原为溶解态的Fe(Ⅱ),并且与硫酸盐还原产生的H_2S相结合生成CRS和ES,导致CRS和ES在柱状沉积物底部积累;同时研究表明,较低的硫化度和矿化度,活性铁不是还原性无机硫累积的限制因子。  相似文献   
132.
2018年1月,利用颗粒物采样器采集武汉市大气PM2.5样品并进行水溶性无机离子(F-、Cl-、NO3-、SO42-、Na+、NH4+、K+、Mg2+、Ca2+)的分析.结果表明,NO3-、SO42-、NH4+是PM2.5中最主要的3种水溶性无机离子,除Mg2+与Ca2+外,PM2.5与WSⅡs (水溶性无机离子)之间的相关性显著,且移动源贡献占主导地位.阴阳离子平衡表明武汉市冬季灰霾期PM2.5呈中性或弱酸性.通过混合单粒子拉格朗日综合轨迹模式模拟并采用分层聚类得出了4种主要的后向气流轨迹及相应的PM2.5和水溶性离子浓度,结果表明区域传输对此次灰霾期影响较大.  相似文献   
133.
坡缕石粘土的磷吸附机制及其铁负载效果研究   总被引:2,自引:0,他引:2  
比较了3种天然坡缕石粘土对不同程度磷污染水体的吸附净化能力,通过等温吸附实验和吸附动力学实验探讨了坡缕石粘土的磷吸附机制,并研究了不同形态铁负载对坡缕石粘土吸附净化磷污染水体性能和机制的影响.结果发现,3种天然坡缕石粘土对不同程度磷污染水体均有一定的吸附净化能力,其中含白云石较多的坡缕石粘土的磷吸附能力最强,吸附等温曲线呈S型,且Freundlich方程(R2=0.977 6)比Langmuir方程(R2=0.924 9)拟合效果更好;准一级方程、冥函数方程、抛物线扩散方程、准二级方程均能较好地模拟坡缕石粘土对磷的吸附动力学过程,说明坡缕石粘土对磷的吸附可能属于不均匀介质的多分子层吸附.此外,不同形态铁负载均能显著增强坡缕石粘土对不同程度磷污染水体的吸附净化能力,吸附等温曲线呈L型,Langmnir方程(Fe2 :R2=0.96,Fe3 :R2=0.967 7)比Freundlich方程(Fe2 :R2=0.965 7,Fe3 :R2=0.936 1)能略好地拟合铁负载坡缕石粘土的磷吸附等温结果,说明铁负载坡缕石粘土的磷吸附过程可能是均匀介质的单分子吸附.适量白云石有助于提高坡缕石粘土的磷吸附净化性能,铁负载可能通过改变坡缕石的表面电荷和吸附活性位点来改变其磷吸附机制,从而提高其磷吸附性能.  相似文献   
134.
西江下游溶解无机碳含量的时空变异特征及其输出通量   总被引:12,自引:0,他引:12  
选取西江下游干支流6个样点进行一个完整水文年度的观测分析,利用基本水文水化学参数来揭示河水溶解无机碳(DIC)含量的时空变异特征,并估算流域DIC输出通量.结果表明,西江下游干支流DIC含量受控于流域地质环境和水热条件,变化于0.74~2.40 mmol/L之间,存在明显的时空变异.干支流DIC含量季节变化模式基本一致,呈现汛期(不包括受洪水影响极强的时段)较高、非汛期较低而洪水期最低的变化特征,流域水热条件的季节变化是其根本原因;河水DIC含量的空间变异基本与流域碳酸盐岩空间分布格局一致,干流DIC含量明显高于支流,且向下游呈减小趋势.西江流域DIC输出通量约4.57×1012g/a,汛期和6月洪水贡献分别达84%和40%.全流域DIC侵蚀通量约12.95 g/(m2·a),在世界各流域中居中上水平.  相似文献   
135.
Removal of Lead,Copper, Zinc and Cadmium from Water Using Phosphate Rock   总被引:2,自引:0,他引:2  
Removal of Pb^2+, Cu^2+, Zn^2+ and Cd^2+ from aqueous solutions by sorption on a natural phosphate rock (FAP) was investigated. The effects of the contact time and initial metal concentration were examined in the batch method. The percentage sorption of heavy metals from solution ranges generally between 50% and 99%. The amount of sorbed metal ions follows the order Cu〉Pb〉Cd〉Zn. Heavy metal immobilization was attributed to both surface complexation of metal ions on the surface of FAP grains and partial dissolution and precipitation of a heavy metal-containing phosphate. The very low desorption ratio of heavy metals further supports the effectiveness of FAP as an alternative and low-cost material to remove toxic Pb^2+, Cu^2+, Zn^2+ and Cd^2+ from polluted waters.  相似文献   
136.
Offset of prograde hydrothermal alterations by retrograde reactions is evident in sediments from a piston core (PC6, 8 m long) from the Guaymas Basin, Gulf of California. Geochemical and mineralogical analyses of sediments and pore fluids show superimposed geochemical signals that indicate currently active reactions are modifying previously formed secondary solids. Hydrothermal barite was formed in a previously active flow channel between 150 and 250 cm depth. Hydrothermal gypsum is presently dissolving at depths > 780 cm, below which hydrothermal fluid flow is channeled by a secondary dolomite layer. Thermal stress of organic matter generates hydrothermal gas and petroleum having wide ranges of compositions and maturities. A significant amount of hydrothermally generated oil has been transported laterally through a porous debris flow (approx. 240 cm subbottom), overwhelming the indigenous bituminous matter. Water soluble petroleum constituents have disseminated throughout the cored sediments. From 400 to 700 cm depth the immature organic matter continues to experience thermally-enhanced diagenesis, and an even higher thermal stress has occurred at the bottom of the core. Enhanced bacterial degradation of organic matter has led to depletion of pore water sulfate and enrichment of ammonium (NH4+) in both pore fluid and sediment, resulting in formation of NH4+ bearing secondary clay minerals at depths below 780 cm.  相似文献   
137.
离子色谱法同时测定地质样品中氟氯磷硫   总被引:5,自引:0,他引:5  
陈德勋  梁汉文 《岩矿测试》1991,10(3):189-192199
本文研究了离子色谱同时测定地质样品中F~-、Cl~-、PO_4~(3-)、SO_4~(2-)的前处理过程,选择了色谱测定最佳条件。在Na_2CO_3全熔的样品溶液中,加入(NH_4)_2CO_3使Si、Al随大多数金属离子同时沉淀;再用预处理柱除去熔剂引入的大量Na~+及CO_3~(2-)消除其干扰;并在流出液中补加相应试剂与淋洗液相匹配,实现了多种地质样品中F~-、Cl~-、PO_4~(3-)和SO_4~(2-)的测定。方法检出限(3s,μg/ml)分别为F~-0.05、Cl~-0.1、PO_4~(3-)0.3、SO_4~(2-)0.5。测定范围为F~-0.05—3μg/ml,Cl~-0.1—6μg/ml,PO_4~(3-)0.3 —30μg/ml,SO_4~(2-)0.5—30μg/ml。  相似文献   
138.
Cr(III) sorbed at the solid/water interface of latex and hectorite was studied by ESR spectroscopy in the presence of different inorganic ligands. The ESR spectra of the surface obtained in the presence of selenite, phosphate and fluoride can be explained in terms of ternary surface complex formation. This is contrasted by the behaviour of sulfate and selenate ions which were found to have no effect on the ligand field of Cr(III), either in the adsorbed state or in solution.  相似文献   
139.
多元分析法在无机多组份光度分析中的应用   总被引:2,自引:0,他引:2  
倪永年 《岩矿测试》1990,9(3):227-233
本文介绍了一些多元分析法,诸如多元线性回归、主成份分析、因子分析、偏最小二乘、聚类分析等方法的基本原理及各自的特点,并就这些方法的近代进展及在无机多组份光度分析中的应用作了综述。  相似文献   
140.
Water samples were collected from the Truckee River-Pyramid Lake system, the Walker River-Walker Lake system, and the Carson River, all located in eastern California and western Nevada, U.S.A., at three different times (i.e., summer 1991, spring 1992, and autumn 1992) over a two year period. The concentrations of As, Na, Cl, PO4, and pH were measured in these river samples and the associated terminal lakes. Arsenic values ranged from below 13 nmol/kg near Truckee, California to 160 nmol/kg at Nixon, Nevada in the Truckee River, from 40 nmol/kg in the headwaters of both West and East Walker Rivers to 270 nmol/kg below Weber Reservoir on the main branch of the Walker River, and from <27 nmol/kg to 234 nmol/kg for the lower Carson River system. Arsenic concentrations in Steamboat Creek (0.91 mol/kg–1.80 mol/kg) in the Truckee River catchment are above the U.S. EPA drinking water maximum contaminant level of 0.67 mol/kg, as are the As concentrations in both Pyramid Lake (1.33 mol/kg–1.57 mol/kg ) and Walker Lake (13.7 mol/kg–18.7 mol/kg). Sources of As for all three rivers include weathering of As-rich rocks and/or regolith and input of high-As geothermal spring waters, both processes primarily, although not exclusively, adding As to the headwater regions of these rivers. Steamboat Hot Springs (29 mol/kg As 54.5 mol/kg), for example, is identified as a source of As to the Truckee River via Steamboat Creek. The high As concentrations in Pyramid and Walker Lakes are likely due to (1) desorption of arsenate from aquatic particulate matter in these high pH waters (9.0 pH 9.5), (2) limited biologic uptake of arsenate, and (3) evaporative concentration of the lake waters. Evaluation of molar PO4}/As ratios of river waters and geothermal spring waters (e.g., Steamboat Hot Springs), indicates that phosphate is substantially enriched in Steamboat Creek as well as the mid to lower reaches of the Walker and Carson Rivers. These regions of each river are dominated by agricultural interests and, additionally, in the case of Steamboat Creek, residential areas and golf courses. Our data strongly imply that phosphate-rich agricultural return flow has likely added P to these streams and, consequently, increased their respective P:As ratios.  相似文献   
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