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1.
贵州水银洞卡林型金矿床金的赋存状态初步研究 总被引：9，自引：0，他引：9
采用电子探针背散射电子图像、波谱和能谱分析技术,对贵州水银洞卡林型金矿床原生富矿石中的含砷黄铁矿Au、As等元素含量及其分布规律进行了系统研究.结果发现有两种金的赋存形式:①不可见金,主要赋存在含砷黄铁矿之中,Au与As之间呈楔形分布关系,推测金以化学结合态金(Au )的形式进入含砷黄铁矿的结构;②显微-次显微自然金颗粒(0.1～6 靘),分布在含砷黄铁矿的边缘.提出含金-砷黄铁矿的形成可能与含Au热液-岩石相互作用过程中含Fe碳酸盐矿物溶解释放Fe有关,含Fe碳酸盐赋矿围岩是形成高品位、大型卡林型金矿床最重要的控制因素之一,与去碳酸盐化有关的碳酸盐脉可能是寻找深部隐伏卡林型金矿体的重要标志. 相似文献
2.
甘肃礼县-岷县成矿带西段寨上金矿床中自然金的发现及成因意义 总被引：4，自引：1，他引：3
位于西秦岭礼(县)-岷(县)成矿带西段的寨上金矿床是近年发现的一个大型微细浸染型金矿。在研究甘肃寨上金矿床物质组分的过程中,采用显微镜观察、电子探针扫描、化学分析等综合分析技术发现了显微自然金颗粒。矿石中的自然金颗粒形态多样,粒度变化较大(5～150μm)。电子探针分析结果显示,自然金中Au=88.23%～92.73%,Ag=7.41%～9.08%,为含银自然金,成色905～926。金的载体矿物有砷黄铁矿、方铅矿、碲汞矿、铁白云石等。金的嵌布类型有粒间金、裂隙金和连生金3种。赋矿围岩中含Fe碳酸盐矿物溶解释放出Fe和溶解Fe的大量硫化物化,可能是寨上金矿床中存在显微可见自然金的最重要因素。 相似文献
3.
4.
甘肃岷县寨上特大型金矿次显微金的赋存状态研究 总被引：4，自引：0，他引：4
寨上金矿是一微细浸染型超大型金矿床。通过光学显微镜、人工重砂、电子探针、扫描电镜等显微测试手段对寨上矿区主要载金矿物进行分析测试得出：黄铁矿、白钨矿是最主要的载金矿物之一,石英、褐铁矿、辉铜矿是次要的载金矿物．方解石、菱铁矿、重晶石等不含金。由于受检测手段所限,在含金黄铁矿、白钨矿、石英等矿物中未发现独立金颗粒,所以寨上金矿次显微金呈微包裹体形式存在于载金矿物中或呈类质同象替代的原子形式存在。通过研究主要载金矿物黄铁矿中Au、As的关系得出：Au与As呈正相关关系;从具有增生环带结构黄铁矿的内核向增生体S、Fe呈对数下降趋势,Au、As呈对数上升趋势。对比沉积期、热液期形成的黄铁矿主量、微量元素得出S、Fe变化不大,微量As呈线性递增,而Au呈线性递减。 相似文献
5.
《矿物学报》2017,(Z1)
广西田林县八渡金矿床主要产于辉绿岩侵入体中,广泛发育乳白色石英网脉,蚀变辉绿岩体即为金矿体,具有硅化、粘土化、碳酸盐化和硫化物化等卡林型金矿热液蚀变特征。本文采用电子探针(EPMA)背散射电子图像(BSE)、波谱(WDS)和能谱(EDS)分析技术,对该矿床原生矿石中含金硫化物显微岩相学结构以及主量和微量元素含量和分布规律进行了系统研究,认为金主要是以不可见化学结合态金(Au+)的形式赋存于含砷黄铁矿和毒砂之中。含金硫化物与热液交代形成的金红石密切共生,并保留含钛铁辉石或钛铁矿等矿物的假象,金红石的形成是辉绿岩中含钛铁辉石或钛铁矿热液蚀变的产物,含金硫化物形成所需要的Fe来自辉绿岩中含钛辉石或钛铁矿等矿物的溶解,Fe的硫化物化过程是导致含金硫化物形成的重要机制。 相似文献
6.
金属硫化物中次显微金的赋存状态已引起人们的重视。张八岭构造带蚀变构造岩型和石英脉型两类金矿金属硫化物中次显微金质子探针分析显示，Au与As、Fe、S、Cu、Pb呈正相关关系，Au以显微包裹体形式存在于金属硫化物中。与蚀变构造岩型金矿相比，晚期的石英脉型金矿可见自然金含量较高，硫化物中显微包裹体金含量较低，可能预示中低温热液金矿中，不仅普遍存在时空分异的金属硫化物中的类质同象金和自然金，还可能存在一定程度的时空分异的自然金和次显微包裹体金。 相似文献
7.
陕西二台子金矿床黄铁矿的演化特征及成因意义 总被引：5，自引：0，他引：5
陕西南部二台子金矿床是迄今我国发现的为数不多的“卡林型”金矿床。矿体产于中泥盆统古道岭组上部含粉砂、泥岩薄层之碳酸盐岩层内的角砾岩带中。角砾成分与含矿围岩一致。角砾岩受后期热液蚀变作用强烈。大多数显微——超显微金赋存于黄铁矿中。黄铁矿成细微粒状浸染分布于角砾岩及蚀变碳酸盐岩中。七十年代初期该矿区曾作 相似文献
8.
西秦岭地区是中国最重要的金矿矿集区之一,除产出少数夕卡岩型金矿床外,几乎所有的其他金矿床都可归并为造山型、卡林型和类卡林型3种类型。研究表明,西秦岭地区中生代花岗岩主要形成于中晚三叠世,而金矿成矿主要集中在晚三叠世,它们都是华北板块与华南板块碰撞导致的秦岭造山作用的产物。西秦岭地区造山型金矿床主要赋存在泥盆系和石炭系一套复杂的构造变形和区域变质的绿片岩相岩中,主要受北西西向脆韧性剪切带控制,成矿元素组合主要为Au-Ag。矿石中含有大量显微自然金、银金矿,明金可见。成矿流体主要为变质流体。由造山作用引起的强烈构造运动为成矿流体提供了运移通道,为矿质沉淀提供了有利的场所。虽然一些造山型金矿床与中酸性岩体相邻,但矿化与岩浆活动不具直接的成因关系。西秦岭地区卡林型金矿床主要产于轻微变质的寒武系至三叠系沉积岩中,明显受地层、岩性和构造控制。金矿床中的金以超显微金和存在于含砷黄铁矿与毒砂晶格中的固溶体金为主。成矿元素组合为Au-As-Hg-Sb-Ba。成矿流体由早期形成的地层水被后期大气降水补给活化形成,也有部分岩浆水或变质水的加入。在伸展背景下大气降水通过循环演化形成了较浅层次的流体系统,导致Au等成矿元素发生沉淀而形成浸染状矿石。西秦岭地区类卡林型金矿床主要产于浅变质沉积岩建造中,受脆韧性剪切带的控制,并形成于花岗岩岩体附近。与造山型、卡林型金矿床最大的不同之处在于,类卡林型金矿床的形成与同时期的岩浆活动有密切的成因关系。矿石中存在显微自然金,载金矿物主要为黄铁矿、含砷黄铁矿和碲化物。成矿热液主要是岩浆水与变质水、建造水的混合流体。与造山型金矿床类似,流体不混溶导致类卡林型金矿床的形成。 相似文献
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10.
位于西秦岭礼(县)—岷(县)成矿带西段的寨上金矿床,是近年发现的一个大型微细浸染型金矿。笔者通过显微镜观察、电子探针和扫描分析等综合分析技术,确认金矿床中矿物组成相当丰富,既有大量硫化物、硫盐、氧化物、硫酸盐、碳酸盐、钨酸盐,又有碲化物、自然金属及多金属互化物。除常见矿物为自然金、黄铁矿、黄铜矿、黝铜矿、方铅矿、闪锌矿、辉锑矿、石英、白钨矿、方解石、菱铁矿、铁白云石和重晶石外,笔者还鉴定出在卡林型金矿床较少见的一些矿物,如硫铜锑矿、车轮矿、辉锑铅矿、辉钼矿、碲汞矿、碲镍矿、Cu-Zn-Ni-Sn-Fe的金属互化物和白钨矿等。矿石中矿物种类较多,组成较复杂以及存在显微自然金,构成寨上金矿床的一大特色。赋矿围岩中含Fe碳酸盐矿物溶解释放Fe以及溶解Fe的大量硫化物化,是寨上金矿床中存在显微可见自然金的最重要因素和金沉淀富集的有利条件。 相似文献
11.
在模拟含Zn2 废水中加入Mg2 和Al3 ,以NaOH为沉淀剂,研究金属盐水解即时合成层状双氢氧化物(LDH)去除Zn2 的可行性。详细探讨了体系终点pH值、配料中Mg2 /Zn2 摩尔比值及反应温度和时间对Zn2 去除率的影响,结合X射线衍射分析(XRD)探讨了Zn2 去除机理,并与化学沉淀法进行了比较。结果表明,实验条件下只有pH值显著影响Zn2 去除率(p<0.05),在9.0~11.0范围内去除效果最佳,达99%以上。通过XRD分析结合即时合成法特点,废水中Zn2 主要是在晶体生成阶段以Zn-Mg-Al三元LDH化合物形式被去除的。与化学沉淀法相比,即时合成法效果更好,适用pH值范围更广,用来处理含Zn2 废水更具优势。 相似文献
12.
Based on the principle of synthesis, a new method was put forward to dispose Congo Red anion-containing dyestuff from wastewater and its feasibility was also examined. The principle of the method is described as follows： Mg^2＋ and Al^3＋ are hydrolyzed to form Mg/Al-LDH by adding Mg^2＋, Al^3＋ and NaOH in wastewater containing anion dyestuff, which is selectively intercalated with the interlayer of LDH in order to balance positive structural charge. While Mg^2＋ and Al^3＋ are co-precipitated to form LDH, the anion dyestuff in wastewater will be removed by LDH synthesized in-situ, as is confirmed by X-ray diffraction analysis of settlings and chemical analysis of aqueous samples. In this work, we studied the influence of Mg/Al mole ratio, pH value, time and temperature of reaction on the removal of anion dyestuff and the use of Mg and Al. The experimental results showed the maximum removal efficiency of anion dyestuff could be attained when pH value was 9.0, and Mg/Al mol ratio was 2 ： 1, reaction duration was 2 hours, and the effect of temperature was not remarkable, and the removal efficiency could reach 100%. Meanwhile, the Mg and Al added could be made good use of. This technology has the advantage of extraordinary efficiency of wastewater disposal. 相似文献
13.
在模拟含Cu2+废水中加入Mg2+和Al3+,以NaOH为沉淀剂,研究金属盐水解即时合成层状双氢氧化物去除Cu2+的可行性,同时考察了体系终点pH值、配料中Mg/Cu摩尔比值及反应温度和时间对Cu2+去除率的影响,探讨了Cu2+去除机理及层状双氢氧化物形成过程。结果表明,实验条件下体系终点pH值显著影响Cu2+去除率,在pH值8.0~11.0范围内去除效果较好,达99%以上。通过X射线衍射分析结合即时合成法特点,废水中Cu2+主要是在晶核生成阶段以Cu/Mg/Al三元层状双氢氧化物形式被去除;三元层状双氢氧化物的形成由反应体系中Al3+、Cu2+、Mg2+分步水解导致,最适pH值约为9.0。 相似文献
14.
Based on the principle of synthesis, a new method was put forward to dispose Congo Red anion-containing dyestuff from wastewater
and its feasibility was also examined. The principle of the method is described as follows: Mg2+ and Al3+ are hydrolyzed to form Mg/Al-LDH by adding Mg2+, Al3+ and NaOH in wastewater containing anion dyestuff, which is selectively intercalated with the interlayer of LDH in order to
balance positive structural charge. While Mg2+ and Al3+ are co-precipitated to form LDH, the anion dyestuff in wastewater will be removed by LDH synthesized in-situ, as is confirmed by X-ray diffraction analysis of settlings and chemical analysis of aqueous samples. In this work, we studied
the influence of Mg/Al mole ratio, pH value, time and temperature of reaction on the removal of anion dyestuff and the use
of Mg and Al. The experimental results showed the maximum removal efficiency of anion dyestuff could be attained when pH value
was 9.0, and Mg/Al mol ratio was 2: 1, reaction duration was 2 hours, and the effect of temperature was not remarkable, and
the removal efficiency could reach 100%. Meanwhile, the Mg and Al added could be made good use of. This technology has the
advantage of extraordinary efficiency of wastewater disposal.
Foundation item: Project supported by the National Natural Science Foundation of China (40472026). 相似文献
15.
M. Tamzid Rahman T. Kameda S. Kumagai T. Yoshioka 《International Journal of Environmental Science and Technology》2018,15(2):263-272
Health hazards from heavy metal pollution in water systems are a global environmental problem. Of similar concern is sludge that results from wastewater treatment due to unsatisfactory sludge management technology. Therefore, the effectiveness of using Mg–Al-layered double hydroxide in the removal of heavy metals from mine wastewater was tested and compared with that of calcium hydroxide [Ca(OH)2], which is a common treatment method for heavy metal removal. Initially, the mine wastewater contained cations of the heavy metals iron (Fe), zinc (Zn), copper (Cu), and lead (Pb). The Mg–Al-layered double hydroxides were able to remove 371, 7.2, 121, and 0.4 mg/L of these pollutants, respectively, using the co-precipitation method. The removal of these metals is most effective using 0.5 g Mg–Al-layered double hydroxide (Mg/Al molar ratio 4) and 20 min of shaking. Zn was removed by the formation of Zn(NO3)(OH)·H2O and Zn5(NO3)2(OH)8 when LDH, Mg/Al molar ratios of 4 and 2, respectively, were used. Similarly, Fe, Cu, and Pb were removed by the formation of Fe–Al-layered double hydroxide, Cu2(OH)3·NO3 and Pb4(OH)4(NO3)4, respectively. While Ca(OH)2 is also capable of reducing the heavy metal concentrations below the Japanese recommended values, this analysis shows that using 0.5 g Mg–Al-layered double hydroxide is a better treatment condition for mine wastewater, because it generates lower sludge volumes than 0.1 g of Ca(OH)2. The measured sludge volume was 1.5 mL for Mg–Al-layered double hydroxide and 2.5 mL for Ca(OH)2, a nearly twofold further reduction. 相似文献
16.
研究了水滑石(LDH)及其焙烧产物(LDO)吸附脱除水溶液中活性深蓝ST-2GLN的性能。考察了pH值、吸附剂投加量、时间等因素对吸附的影响。结果表明:LDH及LDO对活性深蓝ST-2GLN染料具有良好的脱除效果,室温下,1 g/L的LDH和0.5 g/L的LDO对浓度为100 mg/L的染料的脱色率分别达到96.11%和98.58%。pH值是影响吸附能力的关键因素,吸附剂对溶液pH值有一定缓冲作用。LDH及LDO对活性深蓝ST-2GLN吸附结果均符合Langmuir吸附等温式。饱和吸附后的LDH用高温热解法再生,再生产物吸附性能良好,随再生次数增多,脱色率下降。 相似文献
17.
The primary phases and minerals of the Plombières dumps include typical smelting furnace products such as metallic Fe, Pb, Cu, Zn, Fe-Zn alloys, carbides, phosphides, sulfides of Fe, Zn, Pb, Cu, Mn (alabandite), and FeAs. Spinels, mainly of Fe and Al, are common constituents of the primary assemblage; substitution by Zn, V, Cr, Ti, Mg, and Ca occurs. Primary phases also include the most common Zn-rich fayalite, Zn-rich Ca-Fe silicates, melilite, corundum, and apatite. Most of the Zn is incorporated in iron silicates, ZnO and ZnS. Lead occurs mainly as PbS, metallic lead, and is also present in coal residues. Cadmium is found mainly in metallic zinc and its alloys and in ZnO. The dumps also contain mining wastes composed of pyrite, melnikovite, and iron oxides produced by natural weathering of Zn-Pb ores. Melnikovite and iron oxides are rich in As, Pb, and Zn and possess an increased content of Tl. Leaching tests carried out on the surfaces of polished sections indicate that acid rain (solutions I and II) will mobilize mainly Zn and Cd and, to a much smaller extent, Pb and Sb. Leaching of metals by sulfate-chloride fluids present in the pore network of dumps (solutions III, IV, and V) depends on the pH, which in the dumps is controlled by the proportion of carbonates to sulfides. The more acid fluids leach both sulfides and silicates. 相似文献
18.
Gökhan Zengin 《Environmental Earth Sciences》2013,70(7):3031-3041
In this study, the feasibility of using a low-cost adsorbent mixture composed of leonardite (L) and clinoptilolite (C) was evaluated by batch adsorption method using different parameters such as mixing ratio, contact time, pH, temperature, and adsorbent amount for the removal of Zn (II) ions from an aqueous solution. The adsorbents were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and Raman spectroscopy. Additionally, leonardite–clinoptilolite mixture was analyzed by scanning electron microscopy coupled with energy dispersive X-ray. The Zn (II) adsorption along with an unprecedented adsorption capacity of 454.55 mg g?1 for unmodified natural sorbents was obtained by mixing leonardite and clinoptilolite (LC) without any pretreatment at a ratio of 3:1, using 0.1 g of sorbent at a pH 6, for 2 h of contact time. The experimental data showed a good fit for the Langmuir isotherm model. The thermodynamic parameters revealed that the present adsorption process was spontaneous and exothermic in nature (25–50 °C). The kinetic results of the adsorption showed that the Zn (II) adsorption onto the LC follows pseudo-second-order model. The resultant LC mixture has an excellent adsorption capacity of a Zn (II) aqueous solution, and data obtained may form the basis for utilization of LC as an unpretreated low-cost adsorbent for treatment of metalliferous industrial wastewater. 相似文献
19.
Javier Sánchez España Enrique López Pamo Esther Santofimia Pastor Jesús Reyes Andrés Juan Antonio Martín Rubí 《Environmental Geology》2005,49(2):253-266
The geochemical evolution of two acid mine effluents in Tharsis and La Zarza-Perrunal mines (Iberian Pyrite Belt, Huelva, Spain) has been investigated. In origin, these waters present a low pH (2.2 and 3.1) and high concentrations of dissolved sulphate and metals (Fe, Al, Mn, Cu, Zn, As, Cd, Co, Cr, Ni). However, the natural evolution of these acidic waters (which includes the bacterial oxidation of Fe(II) and the subsequent precipitation of Fe(III) minerals) represents an efficient mechanism of attenuation. This self-mitigating process is evidenced by the formation of schwertmannite, which retains most of the iron load and, by sorption, toxic trace elements like As. The later mixing with pristine waters rises the pH and favours the total precipitation of Fe(III) at pH 3.5 and, subsequently, Al compounds at pH 4.5, along with the sorption of trace metals (Mn, Zn, Cu, Cd, Co, Ni) until chemical equilibrium at circumneutral conditions is achieved. 相似文献
20.
Al(III) and Fe(III) binding by humic substances in freshwaters, and implications for trace metal speciation 总被引：2，自引：0，他引：2
Edward Tipping Carlos Rey-Castro Stephen E Bryan John Hamilton-Taylor 《Geochimica et cosmochimica acta》2002,66(18):3211-3224
Published experimental data for Al(III) and Fe(III) binding by fulvic and humic acids can be explained approximately by the Humic Ion-Binding Model VI. The model is based on conventional equilibrium reactions involving protons, metal aquo ions and their first hydrolysis products, and binding sites ranging from abundant ones of low affinity, to rare ones of high affinity, common to all metals. The model can also account for laboratory competition data involving Al(III), Fe(III) and trace elements, supporting the assumption of common binding sites. Field speciation data (116 examples) for Al in acid-to-neutral waters can be accounted for, assuming that 60-70 % (depending upon competition by iron, and the chosen fulvic acid : humic acid ratio) of the dissolved organic carbon (DOC) is due to humic substances, the rest being considered inert with respect to ion binding. After adjustment of the model parameter characterizing binding affinity within acceptable limits, and with the assumption of equilibrium with a relatively soluble form of Fe(OH)3, the model can simulate the results of studies of two freshwater samples, in which concentrations of organically complexed Fe were estimated by kinetic analysis.The model was used to examine the pH dependence of Al and Fe binding by dissolved organic matter (DOM) in freshwaters, by simulating the titration with Ca(OH)2 of an initially acid solution, in equilibrium with solid-phase Al(OH)3 and Fe(OH)3. For the conditions considered, Al, which is present at higher free concentrations than Fe(III), competes significantly for the binding of Fe(III), whereas Fe(III) has little effect on Al binding. The principal form of Al simulated to be bound at low pH is Al3+, AlOH2+ being dominant at pH >6; the principal bound form of Fe(III) is FeOH2+ at all pH values in the range 4-9. Simulations suggest that, in freshwaters, both Al and Fe(III) compete significantly with trace metals (Cu, Zn) for binding by natural organic matter over a wide pH range (4-9). The competition effects are especially strong for a high-affinity trace metal such as Cu, present at low total concentrations (∼1 nM). As a result of these competition effects, high-affinity sites in humic matter may be less important for trace metal binding in the field than they are in laboratory systems involving humic matter that has been treated to remove associated metals. 相似文献