共查询到20条相似文献，搜索用时 149 毫秒
1.
一、引言黄钾铁矾是硫化矿床氧化带最发育的矿物之一,以数量而论,它仅次于褐铁矿而居第二位。如果以矾类矿物而论,可以说是矾中之王。一般来说,在硫化矿床氧化带中或多或少都有黄钾铁矾的存在。祁连山金属硫化矿床中的黄钾铁矾是相当发育的,而某些硫化矿床(例如锡铁山、照壁山等)的氧化带中黄钾铁矾的数量占绝对优势,这种情况在苏联乌拉尔等矿床中也同样见到。黄钾铁矾在质纯量多的情况下经煅烧后可以作研磨原料,亦可制造明矾和肥料之用。 相似文献
2.
黄钾铁矾的形成条件研究及其环境意义 总被引：14，自引：0，他引：14
黄钾铁矾的化学合成实验表明,调整合适的pH值及介质浓度,常温常压下可以实现黄钾铁矾的快速形成。影响黄钾铁矾形成的主要因素包括pH值、温度及硫酸铁介质的浓度。常温下,当pH值在2.60~3.10时,24h内即有黄钾铁矾沉淀出现,2d内则有大量黄钾铁矾生成;在90℃左右时,形成黄钾铁矾的溶液pH值范围增大至1.20~3.10,而且在该范围内,pH值越大越利于黄钾铁矾的形成。高硫酸铁浓度有利于黄钾铁矾的形成,硫酸铁浓度较高(大于0.05M)时,形成较纯的黄钾铁矾矿物;而低浓度时,生成的黄钾铁矾常常含有水绿矾及胶体状的红色无定形羟基硫酸铁杂质。黄钾铁矾的沉淀过程可以用来治理矿山及工业废水,去除其中的S、Fe及As、Cr、Hg、Pb等有毒有害元素。常温常压下黄钾铁矾快速形成的实现为在产生酸性废水的矿山废石堆上形成黄钾铁矾类矿物胶体隔离防渗层提供了良好的潜在应用前景。 相似文献
3.
黄钾铁矾类矿物沉淀去除Cr(Ⅵ)的初步研究 总被引：1，自引：0，他引：1
为探讨黄钾铁矾类矿物沉淀对Cr(Ⅵ)的去除效果,利用黄钾铁矾类矿物沉淀对模拟含Cr(Ⅵ)废水进行了初步实验处理,结果表明,黄钾铁矾类矿物沉淀对含Cr(Ⅵ)废水有较好的去除效果,去除率都在70%以上,最高可达85%。黄钾铁矾与黄铵铁矾沉淀对Cr(Ⅵ)的去除率差别不大;溶液酸碱度对去除率有明显影响,在pH值为2.5~3.2时,时间相同,较高的pH值比低pH值的去除率高。黄钾铁矾类矿物的沉淀过程可用来处理矿山及其他工业废水,去除S、Fe和Cr(Ⅵ)等有毒有害元素。 相似文献
4.
5.
氧化亚铁硫杆菌作用下形成的黄钾铁矾的SEM研究 总被引：29，自引：3，他引：26
黄钾铁矾是金属硫化物在酸性条件下氧化形成的主要次生矿物。很多研究表明,金属硫化物矿区广泛发育的氧化亚铁硫杆菌会影响金属硫化物的氧化分解和次生矿物的形成。为讨论氧化亚铁硫杆菌在黄钾铁矾形成过程中的作用,设计了两组平行实验制备黄钾铁矾：一种采用化学方法合成黄钾铁矾,另一种在相同条件下接种氧化亚铁硫杆菌合成黄钾铁矾。利用X-射线衍射仪(XRD)、扫描电子显微镜(SEM)和能谱分析仪(EDS)等技术对两种实验获得的黄钾铁矾进行定性分析和形貌观察。结果表明：在氧化亚铁硫杆菌充分繁殖的条件下,细菌的参与更利于黄钾铁矾的形成;Fe^2+的氧化速率可能是影响黄钾铁矾结晶的主要因素,氧化亚铁硫杆菌通过提高Fe^2+的供应速度促使黄钾铁矾快速结晶,细菌作用下形成的黄钾铁矾结晶程度好于纯化学方法制备的黄钾铁矾。 相似文献
6.
黄钾铁矾是酸性矿山废水（AMD） 中常见的次生矿物,能有效吸附AMD中Cu、Pb、Zn、Gd、As等重金属元素。不
同条件下形成的黄钾铁矾微形貌不同,其吸附能力也不同。文章通过化学法和微生物法合成了黄钾铁矾,并在粤北大宝山
矿酸性矿山废水中采集了含黄钾铁矾的泥样。利用扫描电镜-能谱分析（SEM） 和X光衍射（XRD）,对三种不同条件下形
成的黄钾铁矾进行鉴定和微形貌特征观察,并分析黄钾铁矾的形成条件。结果表明,常温条件下,pH值2.0~2.5时能够化
学合成黄钾铁矾,其晶体粒径约2~10 μm,且晶形呈板状;而在65℃时,可在pH2.0~3.0之间化学合成黄钾铁矾,但晶形
差。微生物法合成黄钾铁矾pH范围是2.0~5.0,其晶形完好,呈菱面体且晶体大小比较均匀,而约为2~4 μm。酸性矿山废
水中的黄钾铁矾形成的pH值为2.5~3.5,晶形为菱面体形,单个晶体大小多为1~2 μm。根据其形成条件和微形貌特征,文
章推测酸性矿山废水中形成的黄钾铁矾可能是微生物成因。 相似文献
7.
华北克拉通铝(粘)土矿是我国喀斯特型铝(粘)土矿的典型代表,前人针对其物质组成、物质来源、成因机制开展了大量研究,但对其成矿后生改造尚未开展系统研究。本文对嵩箕地区铝(粘)土矿进行了研究,野外剖面显示,含矿岩系由底到顶包括风化壳层、铁质粘土岩、粘土质铝土矿、粘土岩、块状铝土矿层。通过矿物空间穿插关系、X射线衍射、扫描电镜、电子探针分析显示,铝(粘)土矿成矿期主要形成矿物包括硬水铝石、锐钛矿、伊利石、绿泥石等矿物。黄钾铁矾、赤铁矿、针铁矿、高岭石代表了后期改造矿物。矿物垂相分布指示赤铁矿和针铁矿随着深度变浅逐渐减少,硬水铝石在粘土质铝土矿层显著富集,黄钾铁矾广泛分布于铁质粘土岩层和风化壳顶部,穿插于粘土矿物或围绕在硬水铝石周围,以脉状、颗粒状分布,且与伊利石含量呈消长关系。同时,元素地球化学垂相分带显著,大离子亲石元素(Rb、Cs、Ba、Sr)与K2O以及高场强元素(Zr、Hf、Nb、Ta、U、Th)与TiO2显示正相关。铝土矿层中Al2O3明显富集,而SiO2则明显亏损。底板灰... 相似文献
8.
黄钾铁矾是酸性矿山废水（AMD） 中常见的次生矿物，能有效吸附AMD中Cu、Pb、Zn、Gd、As等重金属元素。不
同条件下形成的黄钾铁矾微形貌不同，其吸附能力也不同。文章通过化学法和微生物法合成了黄钾铁矾，并在粤北大宝山
矿酸性矿山废水中采集了含黄钾铁矾的泥样。利用扫描电镜-能谱分析（SEM） 和X光衍射（XRD），对三种不同条件下形
成的黄钾铁矾进行鉴定和微形貌特征观察，并分析黄钾铁矾的形成条件。结果表明，常温条件下，pH值2.0~2.5时能够化
学合成黄钾铁矾，其晶体粒径约2~10 μm，且晶形呈板状；而在65℃时，可在pH2.0~3.0之间化学合成黄钾铁矾，但晶形
差。微生物法合成黄钾铁矾pH范围是2.0~5.0，其晶形完好，呈菱面体且晶体大小比较均匀，而约为2~4 μm。酸性矿山废
水中的黄钾铁矾形成的pH值为2.5~3.5，晶形为菱面体形，单个晶体大小多为1~2 μm。根据其形成条件和微形貌特征，文
章推测酸性矿山废水中形成的黄钾铁矾可能是微生物成因。 相似文献
9.
以广东大宝山铁龙酸性矿山废水(AMD)为研究对象,采集了7个采样点的赭色沉积物样品。利用X射线荧光光谱(XRF)、傅里叶变换红外光谱(FTIR)、X射线粉晶衍射(XRD)和场发射扫描电镜/能谱分析(FESEM/EDS),对AMD中赭色沉积物的矿物相及形貌进行鉴定。现场测定采样点水体物理化学参数(pH/Eh),探讨不同物理化学条件对含铁次生矿物相的影响。结果表明,大宝山铁龙AMD中赭色沉积物的含铁次生矿物主要有施威特曼石、黄钾铁矾、针铁矿、水铁矿等,此外沉积物中还含有七水铁矾、叶绿矾、四水白铁矾、针绿矾、纤铁矾、锡铁山石及羟铝矾等可溶性硫酸盐。施威特曼石具有带骨针棒状、海胆状形貌,针铁矿常呈针状及肾状集合体产出,黄钾铁矾呈六方板状,施威特曼石常可与黄钾铁矾或者针铁矿共生。赭色含铁次生矿物能在AMD较大范围的pH条件下存在,但倾向于Eh高的环境。当pH值增大时,施威特曼石有转变为针铁矿的趋势,并且针铁矿能保存施威特曼石的形貌特征。 相似文献
10.
选取酸性矿坑水环境中常见的次生含铁硫酸盐矿物———黄钾铁矾[KFe3(SO4)2(OH)6]为研究对象,用硫酸盐还原菌
Desulfovibriovulgaris 和异化铁还原菌Shewanellaputrefaciens CN32对其进行还原实验,探讨作为重金属治理潜在材料的
黄钾铁矾的微生物稳定性.实验采用非增长型培养基,在中性、厌氧、30℃的条件下进行.采用湿化学方法测量水溶液及还原产
生的总Fe2+ ,利用X射线衍射(X-raydiffraction,简称XRD)来分析反应后残余固体物质的矿物组成,用扫描电镜(scanning
electronicmicroscopy,简称SEM)观察固体残余物的形貌特征.结果表明,没有微生物的参与,黄钾铁矾的稳定性较好.异化铁
还原菌S.putrefaciens CN32和硫酸还原菌D .vulgaris 在营养极其匮乏的中性厌氧条件下均能还原黄钾铁矾晶格中的
Fe3+ ,显示出黄钾铁矾被微生物还原的可能性.S.putrefaciens CN32还原黄钾铁矾晶格中Fe3+ 的最大还原速率和最终Fe3+
还原率分别为0.001mmol·L-1·h-1和0.37%.与S.putrefaciens CN32不同,D .vulgaris 对黄钾铁矾的还原能力较强,不
含有电子穿梭体(Anthraquinone-2,6-disulfonate,简称AQDS)的实验体系中Fe3+ 的最大还原速率和最终Fe3+ 还原率分别为
0.017mmol·L-1·h-1和16.80%,而添加了AQDS的实验体系的则分别达到了0.026mmol·L-1·h-1和24.30%,这可能与
黄钾铁矾中含有SO42- 有关.D .vulgaris 优先还原黄钾铁矾晶格中的SO42- 产生的H2S是强还原剂,也可促进Fe3+ 的还原,
微生物以及H2S的双重作用可能是导致D .vulgaris 体系中Fe3+ 还原率较高的原因.XRD分析表明,黄钾铁矾经过S.putrefaciens
CN32的作用,物相没有发生变化;而经过D .vulgaris 作用后,黄钾铁矾的特征峰消失,固相残余物中出现了菱铁
矿(FeCO3)、蓝铁矿[Fe3(PO4)2·8H2O]等次生矿物.由于培养基中没有添加任何的磷酸盐,因此蓝铁矿的出现可能是由于培
养基中添加的少量酵母浸膏降解后产生的磷酸根与D .vulgaris 还原黄钾铁矾产生的Fe2+ 相互作用的结果.这些认识对深入
理解地球表层铁的生物地球化学循环具有重要意义,为矿山环境重金属的污染治理提供了实验依据. 相似文献
11.
科克萨依矿床属于区域动力变质热液型金矿。金的赋存形式多样,状态复杂,主要以不规则粒状自然金的形式赋存在石英颗粒裂隙处（裂隙金,51.59%）、石英晶粒间、黄钾铁矾矿物颗粒间、黄铁矿颗粒周边。自然金常附着在残缺细微粒黄铁矿、毒砂的表面。金还与少量的方铅矿、铜蓝伴生,以被包裹的不规则小滴状产出。另外自然金还以鳞片状薄膜状附着在石英脉与绢云母绿泥石片岩的接触面上。 相似文献
12.
13.
The Bereznjakovskoje gold trend, southern Urals, Russia 总被引：2，自引：0，他引：2
B. Lehmann J. Heinhorst U. Hein M. Neumann J. D. Weisser V. Fedesejev 《Mineralium Deposita》1999,34(3):241-249
The East Uralian Zone south of Cheljabinsk consists of a Silurian to Early Carboniferous volcanosedimentary sequence on Proterozoic
basement, intruded by postorogenic Permian granitic rocks. The 7 by 1–2 km Bereznjakovskoje gold trend is hosted by dacitic
to andesitic volcanic-subvolcanic units of Late Devonian age. Epithermal gold mineralization is of the sulfide-rich low-sulfidation
(adularia-sericite) type with the metal spectrum of Au-Ag-As-Sb-Cu-Zn-Pb and a characteristic Te component. Silicic and sericitic
alteration overprints barren propylitic pyrite-rich assemblages in stockworks and shear zones. Precious-metal mineralization
is related to a fahlore-telluride stage overprinting earlier pyrite. Late stage redistribution and weathering liberates gold
from telluride mineral phases with fixation of native gold (high fineness) on vugs and grain boundaries, and in intergrowth
aggregates with supergene jarosite/limonite. Epithermal mineralization formed below the boiling level and is possibly related
to a porphyry system at depth.
Received: 23 February 1998 / Accepted: 12 July 1998 相似文献
14.
Mobilization and attenuation of heavy metals within a nickel mine tailings impoundment near Sudbury, Ontario, Canada 总被引：1，自引：0，他引：1
R. G. McGregor D. W. Blowes J. L. Jambor W. D. Robertson 《Environmental Geology》1998,36(3-4):305-319
The oxidation and the subsequent dissolution of sulfide minerals within the Copper Cliff tailings area have led to the release
of heavy metals such as Fe, Ni, and Co to the tailings pore water. Dissolved concentrations in excess of 10 g/l Fe and 2.2
g/l Ni have been detected within the shallow pore water of the tailings, with increasing depth these concentrations decrease
to or near analytical detection limits. Geochemical modelling of the pore-water chemistry suggests that pH-buffering reactions
are occurring within the shallow oxidized zones, and that secondary phases are precipitating at or near the underlying hardpan
and transition zones. Mineralogical study of the tailings confirmed the presence of goethite, jarosite, gypsum, native sulfur,
and a vermiculite-type clay mineral. Goethite, jarosite, and native sulfur form alteration rims and pseudo-morphs of the sulfide
minerals. Interstitial cements, composed of goethite, jarosite, and gypsum, locally bind the tailings particles, forming hardpan
layers. Microprobe analyses of the goethite indicate that it contains up to 0.6 weight % Ni, suggesting that the goethite
is a repository for Ni. Other sinks detected for heavy metals include jarosite and a vemiculite-type clay mineral which locally
contains up to 1.6 weight % Ni. To estimate the mass and distribution of heavy metals associated with the secondary phases
within the shallow tailings, a series of chemical extractions was completed. The experimental design permitted four fractions
of the tailings to be evaluated independently. These four fractions consisted of a water-soluble, an acid-leachable, and a
reducible fraction, as well as the whole-rock total. Twenty-five percent of the total mass of heavy metals was removed in
the acid-leaching experiments, and 100% of the same components were removed in the reduction experiments. The data suggest
that precipitation/coprecipitation reactions are providing an effective sink for most of the heavy metals released by sulfide
mineral oxidation. In light of these results, potential decommissioning strategies should be evaluated with the recognition
that changing the geochemical conditions may alter the stability of the secondary phases within the shallow tailings.
Received: 9 April 1997 · Accepted: 21 July 1997 相似文献
15.
The upper Amur region comprises weathering crusts (waste mantle developed at copper-nickel sulfide deposits included), which
appreciably hamper the prospecting for such deposits. In order to develop their prospecting criteria, the composition of linear
weathering crusts above a nickeliferous cortlandite dike and barren pyroxenite dike, as well as in the fracture zone above
metamorphic rocks, was investigated. The chemical composition of material in the weathering crust and the mineral composition
of newly formed clay fractions and heavy concentrate were determined. It was established that weathering crust in the nickeliferous
cortlandite dike is characterized by the prevalence of fine jarosite fraction with crystobalite admixture. The heavy concentrate
samples contain jarosite along with a small amount of relict sulfides (pyrite and galena) and native gold. These criteria
can be used in the prospecting for copper-nickel sulfide mineralization in the upper Amur region and other similar regions. 相似文献
16.
Cappadocia Geothermal Province (CGP), central Turkey, consists of nine individual geothermal regions controlled by active regional fault systems. This paper examines the age dating of alteration minerals and the geochemistry (trace elements and isotopes) of the alteration minerals and geothermal waters, to assess the evolution of CGP in relation to regional tectonics. Ar–Ar age data of jarosite and alunite show that the host rocks were exposed to oxidizing conditions near the Earth’s surface at about 5.30 Ma. Based on the δ18O–δD relationhip, water samples had a high altitude meteoric origin. The δ34S values of jarosite and alunite indicate that water samples from the southern part of the study area reached the surface after circulation through volcanic rocks, while northern samples had traveled to the surface after interacting with evaporates at greater depths. REY (rare earth elements and yttrium) diagrams of alteration minerals (especially illite, jarosite and alunite) from rock samples, taken from the same locations as the water samples, display a similar REY pattern to water samples. This suggests that thermal fluids, which reached the surface along a fault zone and caused the mineral alteration in the past, had similar chemical composition to the current geothermal water. The geothermal conceptual model, which defines a volcanically heated reservoir and cap rocks, suggests there are no structural drawbacks to the use of the CGP geothermal system as a resource. However, fluid is insufficient to drive the geothermal system as a result of scanty supply of meteoric water due to evaporation significantly exceeding rainfall. 相似文献
17.
Gold and silver minerals from the Kupol epithermal deposit, Chukotka, were studied. A schematic sequence of mineral formation has been compiled. Specific mineral assemblages have been revealed in jarosite breccias: with native gold, uytenbogaardtite, fischesserite, acanthite, and native sulfur. We considered a possible mechanism of formation of gold and silver sulfides and selenides in volcanogenic deposits: They might have formed during solfatara and postsolfatara processes with the participation of volcanic gases or their condensates and sublimates as well as liquid sulfur (and selenium) and sulfuric hydrotherms produced under the interaction of volcanic gases with meteoric waters. The specific features of the Kupol deposit confirm the solfatara genesis of Au–Ag sulfides and selenides. 相似文献
18.
《Applied Geochemistry》2000,15(8):1219-1244
Arsenian pyrite, formed during Cretaceous gold mineralization, is the primary source of As along the Melones fault zone in the southern Mother Lode Gold District of California. Mine tailings and associated weathering products from partially submerged inactive gold mines at Don Pedro Reservoir, on the Tuolumne River, contain ∼20–1300 ppm As. The highest concentrations are in weathering crusts from the Clio mine and nearby outcrops which contain goethite or jarosite. As is concentrated up to 2150 ppm in the fine-grained (<63 μm) fraction of these Fe-rich weathering products.Individual pyrite grains in albite-chlorite schists of the Clio mine tailings contain an average of 1.2 wt.% As. Pyrite grains are coarsely zoned, with local As concentrations ranging from ∼0 to 5 wt.%. Electron microprobe, transmission electron microscope, and extended X-ray absorption fine-structure spectroscopy (EXAFS) analyses indicate that As substitutes for S in pyrite and is not present as inclusions of arsenopyrite or other As-bearing phases. Comparison with simulated EXAFS spectra demonstrates that As atoms are locally clustered in the pyrite lattice and that the unit cell of arsenian pyrite is expanded by ∼2.6% relative to pure pyrite. During weathering, clustered substitution of As into pyrite may be responsible for accelerating oxidation, hydrolysis, and dissolution of arsenian pyrite relative to pure pyrite in weathered tailings. Arsenic K-edge EXAFS analysis of the fine-grained Fe-rich weathering products are consistent with corner-sharing between As(V) tetrahedra and Fe(III)-octahedra. Determinations of nearest-neighbor distances and atomic identities, generated from least-squares fitting algorithms to spectral data, indicate that arsenate tetrahedra are sorbed on goethite mineral surfaces but substitute for SO4 in jarosite. Erosional transport of As-bearing goethite and jarosite to Don Pedro Reservoir increases the potential for As mobility and bioavailability by desorption or dissolution. Both the substrate minerals and dissolved As species are expected to respond to seasonal changes in lake chemistry caused by thermal stratification and turnover within the monomictic Don Pedro Reservoir. Arsenic is predicted to be most bioavailable and toxic in the reservoir’s summer hypolimnion. 相似文献
19.
Batoul Taghipour Farid Moore Mohammad Ali Mackizadeh 《Chemie der Erde / Geochemistry》2010,70(4):377-384
The Rangan area is part of Cenozoic magmatic belt of central Iran. Eocene volcanic flows and pyroclastic rocks are intruded by a Neogene rhyolitic dome along the major Qom–Zefreh fault. The dome is pervasively hydrothermally altered. The main mineral assemblage is jarosite+barite+pyrite+quartz+sericite. This assemblage indicates acid sulphate or advanced argillic alteration. Sulfur and oxygen isotope data (δ34S & δ18O (SO4)) obtained from jarosite and barite indicate a mixing episode during the evolution of hydrothermal system and reflect the overlapping of two distinct sources of acid sulphate alteration in Rangan, i.e., a magmatic–hydrothermal fluid reacting with steam-heated meteoric water. Considering the position of brittle–ductile transition and major fault movements, jarosite and barite seemingly precipitated from rapid injection of magmatic–hydrothermal fluids into the upper portions of a steam-heated environment. 相似文献
20.
Hydrothermal quartz veins associated with gold and silver mineralization and variable amounts of base metal sulfides have been discovered within an active geothermal system in the Megala Therma area of northern Lesbos. This geothermal system is probably a late evolutionary stage in the formation of this mineralization. The veins are hosted in Upper Miocene volcanic rocks of andesitic composition and consist of quartz, adularia, chlorite, sericite, illite, kaolinite, baryte, small amounts of jarosite and alunite, and native gold, pyrite, galena, sphalerite, chalcopyrite, bornite, chalcocite, covellite and goethite. The principal types of alteration which occur in the studied area are: silicification, propylitization, argillic alteration and potassic, phyllic alteration. 相似文献