胃肠酸度下中药及补铁制剂中铁活性的影响研究     

刘淑娟  王达成  杨沁羽 《华东地质学院学报》2006,29(2):159-163

在人体胃肠液的酸度条件下,采用正辛醇-水分配体系模拟药物在人体肠胃中的分配情况,研究了中药和补铁制剂中铁的形态及其在人体内的吸收情况,并探讨了中药不同比例的配伍、胃肠酸度及还原性物质的存在对水溶态铁和醇溶态铁的影响。结果表明,药物溶液中的铁形态与药物本身特性和配伍情况有关,酸度及配伍对药物中铁的溶出率和溶液中铁的形态有较大影响,人体对铁的吸收与胃肠酸度和还原性物质的存在有关。  相似文献   

邻苯二酚螯合树脂的合成及水样中铝的测定     

于涛  耿伟  杨枝  曹维鹏 《华东地质学院学报》2006,29(3):265-268

合成并表征了新螯合树脂———邻苯二酚螯合树脂(XAD-2-Catechol),研究了XAD-2-Catechol吸附铝的特性和茜素红-铝的显色反应,在pH4.5的HAc-NaAc缓冲介质中,茜素红和铝(Ⅲ)反应生成红色络合物,λm ax=500 nm,铝的含量在0-50μg/25 mL内符合比耳定律。建立了邻苯二酚螯合树脂分离/富集-茜素红分光光度法测定天然水样中铝的新方法,对水样中铝形态进行测定,结果满意。  相似文献   

环境样品中痕量元素的化学形态分析Ⅰ．分析技术在化学形态分析中的应用   总被引：21，自引：7，他引：21  

何红蓼 李冰杨红霞  倪哲明 《岩矿测试》2005,24(1):51-58

文章介绍了形态分析的基本概念,常用的联用分析技术,如气相色谱原子吸收光谱、气相色谱原子荧光光谱、气相色谱微波诱导等离子体原子发射光谱、气相色谱电感耦合等离子体质谱、高效液相色谱电感耦合等离子体质谱等在环境样品(水、土壤、沉积物)中痕量元素化学形态(价态、金属有机化合物等)分析中的应用,土壤和沉积物中污染元素的顺序提取步骤,以形态分析发展动态。引用文献72篇。  相似文献   

环境样品中痕量元素的化学形态分析Ⅱ．砷汞镉锡铅硒铬的形态分析   总被引：2，自引：6，他引：2  

何红蓼  倪哲明李冰 杨红霞 《岩矿测试》2005,24(2):118-128

环境中元素的生物有效性和毒性依赖于其存在的化学形态。文章依据文献的有关报道介绍砷、汞、镉、锡、铅、硒和铬在环境中的分布、毒性及它们在环境样品如水、土壤、沉积物和生物体中的形态分析方法,包括分析物的保存、提取、分离和检测。引用文献120篇。  相似文献   

Rare earth elements in waters from the albitite-bearing granodiorites of Central Sardinia, Italy   总被引：1，自引：0，他引：1  

Riccardo BiddauRosa Cidu  Franco Frau 《Chemical Geology》2002,182(1):1-14

With the aim of contributing to the knowledge of the geochemical behaviour and mobility of the rare earth element (REE) in the natural water systems, the ground and surface waters of the Ottana-Orani area (Central Sardinia, Italy) were sampled. The study area consists of albititic bodies included in Hercynian granodiorites. The waters have pH in the range of 6.0-8.6, total dissolved solid (TDS) of between 0.1 and 0.6 g/l, and major cation composition dominated by Ca and Na, whereas predominant anions are Cl and/or HCO₃.The pH and the major-element composition of the waters are the factors affecting the concentration of REE in solution. The concentrations of ∑REE+Y in the samples filtered at 0.4 μm vary between 140 and 1600 ng/l, with La of between 14 and 314 ng/l, and Yb of between <6 and 12 ng/l. A negative Ce anomaly, especially marked at high pH, is observed in the groundwaters. The surface waters show lower REE concentrations, which are independent of pH, and negligible Ce anomaly.Speciation calculations, carried out with the EQ3NR computer program, showed that the complexes with the CO₃²⁻ ligand are the dominant REE species at pH in the range of 6.7-8.6. The REE³⁺ ions dominate the speciation at pH <6.7 and only in the light REE (LREE).The relative concentrations of REE in water roughly reflect those in the aquifer host rocks. However, when concentrations of REE in water are normalised relative to the parent rocks, a preferential fractionation of heavy REE (HREE) into the water phase can be observed, suggesting the greater mobility and stability of HREE in aqueous solution.  相似文献   

原子荧光光谱法测定芦荟中砷和硒   总被引：5，自引：1，他引：5       下载免费PDF全文

林章金 《岩矿测试》2003,22(3):237-238

应用AFS 820型双道原子荧光仪测定芦荟中砷和硒,方法检出限分别为As0.51μg/L;Se0.42μg/L。经国家一级植物标准物质分析验证,结果与标准值相符。5次测定相对标准偏差As<2.3%;Se<3.1%。  相似文献   

硒在干酪根中的两种不同赋存状态:TEM证据   总被引：9，自引：0，他引：9  

温汉捷  裘愉卓  刘世荣 《地球化学》2003,32(1):21-28

对拉尔玛Se—Au矿床和渔塘坝硒矿床中干酪根的高分辨透射电镜(TEM)研究表明，两个矿床的Se在干酪根中的赋存状态是截然不同的。前者Se在干酪根中的富集可能主要以有机结合态的形式存在，主要是取代干酪根中的硫；而后者Se在干酪根中的富集主要以超微包体Se的形式吸附在干酪根中。两种不同的赋存状态可能主要取决于干酪根中硫含量的多少以及成矿时氧化还原条件的变化。研究表明，TEM是研究元素在干酪根中赋存状态的有效手段。  相似文献   

Mechanisms of physico-chemical interaction of mercury with river sediments from a gold mining region in Brazil: Relative mobility of mercury species     

R. Melamed  R.C. Villas Bas  G.O. Gonalves  E.C. Paiva 《Journal of Geochemical Exploration》1997,58(2-3)

Mercury accumulation in the food chain, as a consequence of gold recovery in Brazil, has been an issue of concern. Reactions of Hg in the environment are quite complex, and can involve various Hg chemical species. Laboratory experiments were carried out on Hg⁰ solubility, Hg complexation and sorption on river sediments from a gold mining region in Brazil. The reactivity and the mobility of Hg species were considered. Results indicate that methyl mercury is more mobile than ionic mercury, and that the presence of humic acid enhances drastically the solubility of Hg⁰. The soluble complex formed has a relatively lower interaction at the sediment/water interface and is more prone to spread through the aquatic environment.  相似文献   

Mercury mobility at the Carson River Superfund Site, west-central Nevada, USA: Interpretation of mercury speciation data in mill tailings, soils, and sediments     

Paul J. Lechler  Jerry R. Miller  Liang-Chi Hsu  Mario O. Desilets 《Journal of Geochemical Exploration》1997,58(2-3)

The Carson River Superfund Site in west-central Nevada is an area of Hg-contaminated soil, sediment, water, air, and biola resulting from the amalgamation milling of Ag-Au ores of the Comstock lode worked approximately a century ago. In order to develop an understanding of the behavior, transport, and fate of Hg at this site, a technique was developed to estimate the proportions of total, elemental, exchangeable, organic, and sulfide Hg in soils, sediments, and tailings.Results of this analysis performed on active Carson River sediments indicate that Hg is selectively dissolved out of Hg-Au amalgam particles and subsequently adsorbed to fine-grained sediments which are then deposited in downstream, low-energy reaches of the Carson River and Labontan Reservoir. In the relatively more-reducing environment of the reservoir Hg appears to be converted, in large part, to relatively-insoluble HgS.The original elemental form of Hg released to the environment is the chemical form which is still dominant in most highly-contaminated soils, sediments, and tailings. Deeper, more-reducing soil horizons, however, appear to fix a significant portion of the Hg as HgS, analogous to the Lahontan Reservoir example described above. This fixation as HgS is documented to be largely limited to higher-sulfur areas where sulfide minerals from the Comstock ores increase the total sulfur concentrations of contaminated soils, sediments, and tailings.  相似文献   

铜与间氯偶氮安替比林显色反应研究及铜的形态分析     

范华均  谢继云 《岩矿测试》1997,16(1):40-44

在ｐＨ４８的邻苯二甲酸氢钾＿ＮａＯＨ缓冲介质中，Ｃｕ（Ⅱ）与间氯偶氮安替比林形成１∶２的蓝色配合物，其最大吸收峰位于６３０ｎｍ处，表观摩尔吸光系数为４２６×１０４Ｌ·ｍｏｌ－１·ｃｍ－１，Ｃｕ（Ⅱ）的质量浓度在０～２ｍｇ／Ｌ时符合比尔定律。应用该法测定了桃叶及牛肝标样中的铜含量，测定值与标准值一致。结合活性炭分离，建立了铜的形态分析流程，并测定了茶汤中铜的各种主要形态及其分布。  相似文献