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安徽月山矿成矿流体中铜,金的迁移形式和沉淀的物理化学条件 总被引：4，自引：0，他引：4
文章基于矿床地质特征和地球化学热力学理论,计算和讨论了安微月山矽卡岩－热液型铜,金矿田成矿流体中成矿物质的迁移形式和沉淀的物理化学条件,两类矿床的主要成矿阶段,成矿流体中铜主要以氯络合物ＣｕＣｌ、ＣｕＣｌ２＾－、ＣｕＣｌ＾２－３,ＣｕＣｌＯＨ,金主要以硫的络合物Ａｕ２（ＨＳ）２Ｓ＾２－,Ａｕ（ＨＳ）２＾－,ＡｕＨＳ、ＡｕＨ３ＳｉＯ４等形式进行迁移,成矿流体中铜沉淀的主要物化条件是降温及氯离子浓度的 相似文献
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金在碱性富硅热液中溶解和迁移的实验研究 总被引：17，自引：3，他引：17
实验测定了金在碱性富硅溶液中的溶解度，并标定了Ａｕ与ＳｉＯ２之间的配合关系Ａｕ＾＋Ｈ２ＳｉＯ＾－４＝ＡｕＨ３ＳｉＯ＾０４在８０￣２５０℃的温度范围内，其平衡常数为ｌｇＫ＝－１．９８８９＋１００８５。１８／Ｔ（Ｔ为绝对温度）各温度下的平衡常数值与Ａｕ－ＨＣｌ－ＳｉＯ２－Ｈ２Ｏ体系中得到的结果一致。它表明溶液在酸性和碱性条件下，ＳｉＯ２均作为配位体，与Ａｕ形成ＡｕＨ３ＳｉＯ＾０４在热液中溶解、迁移。Ａ 相似文献
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重铬酸钾法测定废水COD条件改进的研究 总被引：3，自引：0，他引：3
本提出用ＣｕＳＯ４作催化剂，在Ｈ２ＳＯ４－Ｈ２ＰＯ４溶液中，重铬酸钾回流测定废水ＣＯＤ的方法，实验表明，最佳测定条件为：ＣｕＳＯ４浓度为７×１０＾－２ｍｏｌ．Ｌ＾－１（混酸溶液）：Ｈ２ＳＯ４：Ｈ３ＰＯ４＝５：１（体积比）回流时间２ｈ，通过与标准方法对比，测定结果满意，本方法的优点是：不需用贵重金试剂Ａｇ２ＳＯ４，改用ＣｕＳＯ４作催化剂，精密度高，准确性好，具有一定的实用价值。 相似文献
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黔西南微细浸染型金矿床金,砷共生分异机制初步研究 总被引：3，自引：0，他引：3
黔西南微细浸染型金矿床成矿热液中金可能主要以Ａｕ（ＨＳ）－２及ＡｕＳ－等迁移形式,砷则主要以Ｈ３ＡｓＯ０３形式迁移。随着成矿热液系统物理化学条件的改变,从成矿前阶段、热液主成矿阶段至晚成矿阶段,金、砷络合物在热液中的沉淀经历了共生、初始分离至分离的富集演化阶段。物理化学条件改变是导致金、砷共生分异的重要因素。 相似文献
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紫木凼含砷微细浸染型金矿床金砷成矿过程初步研究 总被引：5，自引：3，他引：2
紫木凼含砷微细浸染型金矿床两个钻孔不同深度金、砷及伴生元素含量变化特征研究结果表明,在矿床深部金与砷密切共生,表现为正相关;而在矿床浅部金与砷关系并不密切,二者不相关或呈负相关,金矿床成矿热液中金可能主要以Ａｕ（ＨＳ）２及ＡｕＳ等形式迁移,砷则主要以Ｈ３ＡｓＯ３形式迁移。随着成矿热液系统物理化学条件的改变,从成矿前阶段、热液主成矿阶段至晚成矿阶段,金、砷络合物在热液中的沉淀经历了共生、初始分离至分 相似文献
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高寒干旱地区金矿氧化带金的次生富集机理 总被引：3，自引：1，他引：2
探讨了高寒干旱气候条件下,金矿氧化带金的迁移形式、方向和次生富集机理。毛细管作用使Ａｕ（Ｓ２Ｏ３）３－２配合物向上迁移至近地表处,该配合物中Ｓ２Ｏ２－３被氧化成ＳＯ２－４,Ａｕ＋岐化或被还原为Ａｕ０富集 相似文献
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硫脲浸取—光度法测定硫化矿中金 总被引：3，自引：0，他引：3
常温下在Ｈ２Ｃ２Ｏ４－Ｈ２ＳＯ４介绍中,用５０ｇ／Ｌ硫脲（Ｔｕ）溶液可完全浸提含金硫化矿中Ａｕ,对金的浸取率可达９９．８％,然后作用ＣＬ－Ｐ２０４萃淋树脂事集含金分解液中Ａｕ（Ｔｕ）２＾＋,结晶紫分光度法测定。方法用于硫化原生矿及含硫浮选精矿中Ａｕ的测定,所得结果与王水分解原子吸收法测定相符,其ＲＳＤ（ｎ＝５）〈３％。 相似文献
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热泉热液金矿化中嗜热微生物——有机质的地球化学作用 总被引：3，自引：0，他引：3
本文主要通过对热泉热液金成矿过程中的热泉水化学成分和组分的分析,得出泉水中金与氮磷硫、氟硅碳两组组分有很好的相关性。嗜热硫酸盐还原菌能使［Ａｕ（ＨＳ）２］－和［Ａｕ（Ｓ２Ｏ３）２］３－都氧化还原成硫化物,从而使金由热水溶液中沉淀。热泉沉积软泥的有机质中的含硫氨基酸、含硫芳烃也起到了一定的聚金作用。 相似文献
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东坪金矿床的围岩蚀变和流体特征 总被引：1，自引：0，他引：1
东坪金矿床围岩蚀变特征、流体包裹体特征与氢氧同位素特征研究表明，成矿流体富集Ｋ＾＋，Ｎａ＾＋，Ａｕ＾＋，Ｃｌ＾－和ＣＯ２、Ｈ２Ｓ成矿溶液以岩浆热液为主，但有天水的混合。金在溶液中以Ａｕ（ＨＳ）＾－２和ＡｕＣｌ＾－２形式存在，构造活动引起的压力突变和流岩反应是引起金沉淀的主要因素。 相似文献
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Gold nuggets (centimetre scale) have formed in a supergene alteration zone on hydrothermal gold deposits, and occur intergrown with quartz and iron oxyhydroxide pseudomorphs after sulphide minerals, and along fractures in quartz and host rocks. The supergene alteration was driven by groundwater-driven water-rock interaction near to a regional unconformity beneath fluvial sediments, and involved clay alteration and oxidation that extended up to 50 m below the unconformity. Oxidation of pyrite and arsenopyrite produced temporary thiosulphate ligands that mobilised microparticulate gold encapsulated in the sulphide minerals. The nuggets have some crystalline form, and internally they consist of anhedral grains, elongated gold plates, and intimate intergrowths of gold and iron oxyhydroxide. Nugget surfaces have further micron scale overgrowths of microparticulate gold, gold plates, and gold crystals. Nuggets were eroded and recycled into nearby proximal Miocene quartz pebble conglomerates, where they concentrated in placers near the basal unconformity. Later recycling transferred gold into Pleistocene fluvial channels. Gold dissolution and redeposition as plates and crystals occurred on the exterior surfaces of placer gold particles, with little change in mass. All groundwater maintained high pH throughout the geological history because there was sufficient calcite in the basement rocks to neutralise any acid generated by pyrite oxidation. Hence, gold mobility in sediments was driven by thiosulphate complexes as for the in situ nuggets, albeit with lower dissolved sulphur concentrations. Despite aridification of the climate in the late Cenozoic, with resulting localised high dissolved chloride concentrations, chloride complexation did not contribute to gold mobility. 相似文献
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Role of hydrogen peroxide and hydroxyl radical in pyrite oxidation by molecular oxygen 总被引：3，自引：0，他引：3
Martin A.A. Schoonen Andrea D. Harrington Daniel R. Strongin 《Geochimica et cosmochimica acta》2010,74(17):4971-3773
Hydrogen peroxide and hydroxyl radical are readily formed during the oxidation of pyrite with molecular oxygen over a wide range of pH conditions. However, pretreatment of the pyrite surface influences how much of the intermediates are formed and their fate. Acid-washed pyrite produces significant amounts of hydrogen peroxide and hydroxyl radical when suspended in air-saturated water. However, the hydrogen peroxide concentration shows an exponential decrease with time. Suspensions made with partially oxidized pyrite yield significantly lower amounts of hydrogen peroxide product. The presence of Fe(III)-oxide or Fe(III)-hydroxide patches facilitates the conversion of hydrogen peroxide to oxygen and water. Hence, the degree to which a pyrite surface is covered with patches of Fe(III)-oxide or Fe(III)-hydroxide patches is an important control on the concentration of hydrogen peroxide in solution.Hydrogen peroxide appears to be an important intermediate in the four-electron transfer from pyrite to molecular oxygen. Addition of catalase, an enzyme that decomposes hydrogen peroxide to water and molecular oxygen, to a pyrite suspension reduces the oxidation rate by 40%. By contrast, hydroxyl radical does not appear to play a significant role in the oxidation mechanism. It is estimated on the basis of a molecular oxygen and sulfate mass balance that 5-6% of the molecular oxygen is consumed without forming sulfate. 相似文献
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Gold grains were studied in 102 till and gravel samples from an area with Au anomalies in the fine fraction of till. The form and size of gold nuggets were studied under the microscope, and the composition of selected grains was determined on a microprobe. The number of visible nuggets per sample was less than 10 per 81. In size, the nuggets were between 0.07 and 1 mm. Most of them were indefinite but flat in form, although idiomorphic gains were also observed. In composition, the gold grains in bedrock differed somewhat from those in till and gravel. Some of the nuggets found in gravel and in till were probably secondary in origin. The possibility that all the grains are not primary is emphasized in the interpretation of geochemical results. 相似文献
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A rare collection of centimetre-scale proximal gold nuggets has been examined in the context of the Late Pleistocene to Holocene eluvial and colluvial sediments in which they occur, in a range of environments from arid temperate to periglacial. Liberation of supergene nuggets from their basement source in fault zones occurred progressively by physical erosion as the host basement rocks were uplifted between middle Miocene and Holocene. The host sediments are made up of poorly sorted angular greenschist facies schist debris. Some nuggets were recycled through several generations of these colluvial deposits, and additional nuggets were liberated to younger sediments during this time. The nuggets did not migrate laterally more than a few tens of metres during this repeated recycling, and were passively elevated vertically with the rising basement on to the crest and slopes of a 1600 m high mountain range. The most recently liberated nuggets retain almost all the morphological features of their supergene origin, including coarse (cm scale) crystal shapes, delicate crystalline internal structure, and imprints of oxidised pyrite crystals. Minor transport in colluvium has caused some abrasion and rounding of gold crystals. Repeated recycling progressively obscured the crystal shapes, although relict crystals are still recognisable on parts of most nuggets. Differential timing of liberation from basement has resulted in a wide range of rounding effects in groups of closely-coexisting nuggets. Variably crystalline gold overgrowths (micron scale) coat abraded surfaces of all or part of most nuggets, commonly intergrown with authigenic smectite clay minerals. These overgrowths developed from alkaline groundwater (pH 7–9) that had undergone extensive chemical interaction with labile minerals in the host colluvium. Abrasion during recycling removed some of the overgrowths, but this was replaced in the new sedimentary hosts. Physical and chemical processes affecting nuggets in these sediments have similarly affected eluvial and colluvial nuggets in a wide range of settings around the world, including Yukon (Canada), California (USA) and arid parts of Australia. 相似文献
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Hydrogen peroxide interference in chemical oxygen demand during ozone based advanced oxidation of anaerobically digested livestock wastewater 总被引：1，自引：1，他引：0
E. Lee M.Sc H. Lee M.Sc. Y. K. Kim Ph.D. K. Sohn M.Sc. K. Lee Ph.D. 《International Journal of Environmental Science and Technology》2011,8(2):381-388
It is known that hydrogen peroxide interferes with chemical oxygen demand analysis by consuming oxidation agents such as potassium dichromate, thus leading to overestimation of the chemical oxygen demand measurements. The objective of the study was to investigate the effects of hydrogen peroxide interference and to determine true chemical oxygen demand values on interpreting treatment performance during ozone-based advanced oxidation of livestock wastewater in which hydrogen peroxide concentration and chemical oxygen demand values are dynamically changing. According to the chemical oxygen demand monitoring data, chemical oxygen demand values were always higher than the initial chemical oxygen demand load when hydrogen peroxide was involved and the treatment performance with ozone alone or ozone/ultraviolet was better than with coupled hydrogen peroxide. The extent of overestimation was proportional to the remaining hydrogen peroxide concentration and the average overestimation ratio in livestock wastewater was in the range of 0.50～0.58 mg per 1 mg of hydrogen peroxide, depending upon the quality of the wastewater treated. True chemical oxygen demand values were estimated by correlating the extent of overestimation with the remaining hydrogen peroxide concentration during treatment. The extent of overestimation decreased to zero gradually as the amount of hydrogen peroxide also approached zero as oxidation proceeded. The corrected chemical oxygen demand values indicated underlying tendency of oxidation, which could not be seen in the original chemical oxygen demand monitoring data. Application of ozone/hydrogen peroxide was more efficient for reducing chemical oxygen demand than ozone alone, as was ozone/hydrogen peroxide/ultraviolet compared to ozone/ultraviolet. When coupled with ozone, ultraviolet irradiation was more efficient than hydrogen peroxide for decreasing chemical oxygen demand during treatment of livestock wastewater. 相似文献
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W. J. Zhang M. Zhang F. Xiao L. P. Fang D. S. Wang 《International Journal of Environmental Science and Technology》2014,11(3):731-738
Pretreatment of waste emulsions with high organic content by a combined process of vibratory shear enhanced process and Fenton’s oxidation prior to biological treatment was investigated. Vibrating membrane had shown good performance in chemical oxygen demand and oil removals and the mitigation of concentration polarization. However, the permeate after filtration processing still contained high content of organics. Thus, additional Fenton oxidation was applied to reduce the organic loading, and improve the biodegradability of the wastewater. The optimal molar ratio of ferrous iron to hydrogen peroxide was 0.05 obtained from the jar-test experiments. Removal of organics was enhanced by increasing hydrogen peroxide dosage, while efficiency of hydrogen peroxide reached maximum of 1.11(w/w) at the hydrogen peroxide dosage of 6.8 g/L. Furthermore, the biological experiments indicated that the high concentration of organics could inhibit microbial activity, which decreased the chemical oxygen demand degradation rates. The adaptive period of the microbe was greatly shortened using Fenton’s reagent at the low dosages. The improvement of the biodegradability could be explained by partial mineralization and chemical transformation of parent organic compounds after Fenton oxidation. 相似文献
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It is possible that placer gold retains the trace element composition (`signature') of the parent lode. Laser ablation–inductively coupled plasma–mass spectrometry (LA–ICP–MS) offers sensitive detection limits of 59 elements with sub-millimetre sample spot sizes, ideal for signature analysis of placer. Here, the optimum laser parameters, analytical precision and reproducibility of elemental signatures are determined in placer nuggets by infrared LA–ICP–MS. The highest precision was offered by Q-switched ablation at a relatively low energy level, using Au as an internal standard; these parameters gave median precision values of 33–82% RSD for trace elements in nuggets. In addition to major constituents such as Ag, Cu and Hg, placer from several rivers world-wide commonly contained a wide range of trace elements including, in some cases, unusual REE patterns. At least two distinct signatures could be distinguished in placer from most of the rivers examined, while multiple examples of certain signatures were also seen. Tracking these signatures back to their original tributaries may offer a means of identifying the number and approximate location of deposits within a river watershed, thereby significantly aiding exploration. 相似文献
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论文通过对碱泉子金矿床和文峪金矿床成矿地质背景的认识,得出了两矿床的矿床地质特征都显示了明显的造山型热液金矿床的矿床地质特点。在此基础上对比研究了两矿床的流体包裹体特征及氢氧同位素组成特征。研究结果表明,两矿床的成矿流体均以中温、低盐度、高CO2含量为特征,这些特征也吻合了典型的造山型热液金矿床成矿流体的基本特征;两矿床氢氧同位素组成的数据投影点主要落在变质水与岩浆水的混合区附近、并有向大气降水漂移的趋势。基于以上分析结果,推断出两矿床在成矿机制方面也有很大的相似性,并由此探讨了碱泉子金矿床的成矿机制特点。 相似文献