Dissolution of lead- and lead-arsenic-jarosites at pH 2 and 8 and 20 °C: Insights from batch experiments     

Adrian M.L. Smith  William E. Dubbin  Karen A. Hudson-Edwards 《Chemical Geology》2006,229(4):344-361

Lead- and Pb-As-jarosites are minerals common to acidic, sulphate-rich environments, including weathering zones of sulphide ore deposits and acid rock or acid mine drainage (ARD/AMD) sites, and often form on or near galena. The structures of these jarosites are based on linear tetrahedral-octahedral-tetrahedral (T-O-T) sheets, comprised of slightly distorted FeO₆ octahedra and SO₄²⁻ (-AsO₄³⁻ in Pb-As-jarosites) tetrahedra. To better understand the dissolution mechanisms and products of the break down of Pb- and Pb-As-jarosite, preliminary batch dissolution experiments were conducted on synthetic Pb- and Pb-As-jarosite at pH 2 and 20 °C, to mimic environments affected by ARD/AMD, and at pH 8 and 20 °C, to simulate ARD/AMD environments recently remediated with slaked lime (Ca(OH)₂). All four dissolutions are incongruent. Dissolution of Pb-jarosite at pH 2 yields aqueous Pb, Fe and SO₄²⁻. The pH 8 Pb-jarosite dissolution yields aqueous Pb, SO₄²⁻ and poorly crystalline Fe(OH)₃, which does not appear to resorb Pb or SO₄²⁻, possibly due to the low solution pH (3.44-3.54) at the end of the experiment. The pH 2 and 8 dissolutions of Pb-As-jarosite result in the formation of secondary compounds (poorly crystalline PbSO₄ for pH 2 dissolution; poorly crystalline PbSO₄ and Fe(OH)₃ for pH 8 dissolution), which may act as dissolution inhibitors after 250 to 300 h of dissolution. In the pH 2 dissolution, aqueous Fe, SO₄²⁻ and AsO₄³⁻ also form, and in the pH 8 dissolution, Fe(OH)₃ precipitates then subsequently resorbs aqueous AsO₄³⁻. The dissolutions probably proceed by preferred dissolution of the A- and T-sites, which contain Pb, and SO₄²⁻ and AsO₄³⁻, respectively, rather than Fe, which is sterically remote, within the T-O-T Pb- and Pb-As-jarosite structures. These data provide the foundation necessary for further, more detailed investigations into the dissolution of Pb- and Pb-As-jarosites.  相似文献   

Sorption of P by ferric hydroxide film, cover particles of sediments of Lake Baikal     

Alexander Likhoshvay Mikle Grachev 《中国地球化学学报》2006,25(B08):138-139

We investigated in more detail the adsorption phenomenon which was described earlier. It was clearly established that the hydroxyl apatite was not participated in P adsorption. This phenomenon takes place because of ferric hydroxide film. Modem sediments from the Southem Basin of Lake Baikal were taken and stirred with Baikal water. Carrier-free [^32p]-orthophosphate was added in this system. Similar experiments were made with carrier-free [^35S]-sulphate. Sulphate stayed in supematant completely. The influence of pH on the system with inorganic phosphate was also studied. In low alkali conditions phosphate migrated in supematant, in low acid, in sediments. Baikal sediment was stripped of iron-hydroxous film by treatment with 1% oxalic acid. Investigation of striped sediment shown that phosphate stays in supematant only. Hence, hydroxyl apatite cannot be the phase of the sediments of Lake Baikal which binds phosphate. This all showed by our group before. Now we have found the limit of phosphate sorption in Lake Baikal sediments and the stehiometry of the sorption. The sorption limit of Lake Baikal sediments was studied. An experiment with inorganic ^31P phosphate was made. 0.025% K2HPO4 solution with adding ^32P radioactive mark into it was prepared. 100 μL of mixture of ^31PO4^3- and ^32PO4^3- seven times were added in a ＂Baikal water-Baikal sediment＂ system and blank （100 ml BW only）. Concentrations of inorganic ^31PO4^3- were very low so the bend dot on the diagram was found and sorption limit of sediment was estimated. Baikal sediment stopped assimilating phosphate in the bend dot. The stehiometry of sorption was estimated by supematant-sediment radioactive ratio, which equals 3, that is, three Fe （Ⅲ） atoms associate one PO4^3- anion. The only Fe （Ⅲ） substance which could associate P is -Fe-O-Fe- polymer film. It also dissolves in acid conditions.  相似文献   

Kaolinite – alkali interaction and effects on basic properties     

Puvvadi?Venkata?SivapullaiahEmail author  Manju 《Geotechnical and Geological Engineering》2005,23(5):601-614

The influence of type and amount of clays present in soils on their properties is well understood. The clays exert their influence through large specific surface area and charges on them. Their effect is mostly exhibited through inter particle bonding and subsequent particle associations. The mineralogical influence of soils in water is well documented. However, the change in soil water system because of presence some of the contaminants can greatly influence the soil behaviour. Some of the changes are due to formation of new compounds due to interactions between the soil and pollutant. The paper reports the effect of interaction of kaolinite mineral with alkali on the index properties of soils from which the geotechnical behaviour can be understood. Detailed X-ray diffraction studies have shown that sodium aluminum silicate hydroxide hydrate (NASH) is formed by clay alkali reactions. The type and amount of formation of the compound is influenced by the concentration of alkali solution. While the compound formed is in smaller quantities with 1 N NaOH solution, significantly high quantity is formed with 4 N NaOH solution. Presence of alumina is shown to play a significant role. It was observed that the formation of sodium aluminum silicate hydroxide hydrate is reduced in the presence of alumina. Specific gravity of contaminated clay soil was reduced which confirms the formation of new compounds. Water adsorption and specific surface area of soil are also influenced due to soil alkali interaction. The changes in the free swell and index properties of soil in the presence of alkali have been explained by the changes in soil fabric and the formation of new compound.  相似文献   

阴离子树脂预处理-离子色谱法测定核纯氢氧化锂中阴离子杂质     

李伯平  王志龙  徐静  崔建勇  郭冬发 《铀矿地质》2019,(1):33-37,64

采用氨型弱阴离子交换树脂预先对核纯氢氧化锂溶液转型,消除核纯氢氧化锂溶液中的游离氢氧根基体,转型后的溶液采用阴离子色谱法同时测定杂质氟离子、氯离子和硫酸根离子。该方法获得的氟离子、氯离子和硫酸根离子加标回收率优于90%,对应检出限分别为:5.0μg/g、 11.0μg/g和24.0μg/g。  相似文献   

以碱式氯化镁为前驱体制备棒状氢氧化镁阻燃剂   总被引：1，自引：0，他引：1       下载免费PDF全文

张波  李丽娟  聂峰  曾忠民  宋富根  姬连敏  刘志启  贾旭宏 《盐湖研究》2010,18(2)

氢氧化镁作为一种阻燃剂,由于其无毒无味、绿色环保及高效阻燃性而受到全球的广泛关注。棒状氢氧化镁由于其特殊的形貌,在添加到材料中后有助于改善材料的轴向应力。介绍了一种以碱式氯化镁为前驱体制备棒状氢氧化镁的方法,并对制备的棒状氢氧化镁进行了物理性能表征。  相似文献   

Rare earth element and yttrium compositions of the Paleoproterozoic Yuanjiacun BIF in the Lüliang area and their implications for the Great Oxidation Event(GOE)     

ChangLe Wang  LianChang Zhang  CaiYun Lan  YanPei Dai 《中国科学:地球科学(英文版)》2014,57(10):2469-2485

In China, most Precambrian banded iron formations(BIFs) are situated in the North China Craton. The Yuanjiacun iron deposit, located in the Lüliang area, is arguably the most representative Superior-type BIF. This iron deposit is coherent with the sedimentary rock succession of the Yuanjiacun Formation in the lower Lüliang Group, and was interpreted to be deposited at 2.3–2.1 Ga, based on ages of overlying and underlying volcanic strata. This age overlaps with the time range of the Great Oxidation Event(GOE, 2.4–2.2 Ga). The Yuanjiacun BIF consists mainly of subhedral-xenomorphic magnetite and quartz and rarely other minerals with a lower degree of metamorphism, from greenschist to lower amphibolite facies. The geochemical characteristics of this BIF are similar to those of Superior-type BIFs. Prominent positive La, Y, and Eu anomalies normalized by the Post Archean Australian Shale(PAAS) indicate that the primary chemical precipitate is a result of solutions that represent mixtures of seawater and high-T hydrothermal fluids. The contamination from crustal detritus found is negligible based on low abundances of Al2O3 and TiO2(0.5%) and of trace elements such as Th, Hf, Zr, and Sc(1.5 ppm), as well as the lack of co-variations between Al2O3 and TiO2. In particular, the Yuanjiacun BIF samples do not display significant negative Ce anomalies like those of the Archean iron formations, but rather, the Yuanjiacun BIF samples exhibit prominent positive Ce anomalies, low Y/Ho ratios, and high light to heavy REE((Pr/Yb)SN) ratios, which are essentially consistent with the late Paleoproterozoic(2.0 Ga) BIFs around the world. These characteristics of the Yuanjiacun BIF samples imply that the ancient ocean(2.3–2.1 Ga) was redox-stratified from oxic shallow water to deeper anoxic water. The specific redox conditions of the ancient ocean may be related to the GOE, which gave rise to the oxidation of Ce and Mn in the upper water, and to the presence of a Mn oxide shuttle in the ocean, resulting in varying REE patterns due to the precipitation and dissolution of this Mn oxide shuttle under different redox states. Therefore, the Yuanjiacun BIF appears to have formed near the redoxcline and lower-level reduced marine water.  相似文献