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1.
银洞坡金矿位于桐柏县围山城金银矿带的中部,为一超大型金矿床,伴生银、铅锌。对金矿石中主要成矿阶段流体包裹体进行了详细的岩相学、显微测温及激光拉曼光谱成分研究,结果表明：金矿石中发育气液两相包裹体、富气相包裹体和含CO2三相包裹体,流体成分为H2O NaCl CO2体系,含少量N2、CH4、H2S和H2。流体不混溶是导致矿质沉淀的主要因素。3类包裹体的均一温度为1692～3992 ℃,流体盐度为18%～122%,其中含CO2三相包裹体的盐度明显小于气液两相包裹体的盐度。利用不混溶体系估算得到包裹体的捕获压力为62～1263 MPa,成矿深度为52 km左右。矿石中黄铁矿的δ34S为16‰~33‰,围岩中纹层状黄铁矿的δ34S为33‰～62‰,矿石中的δ34S小于围岩中δ34S值,表明成矿物质中的硫可能来源于地幔硫和围岩硫的混合。 相似文献
2.
《西北地质》2019,(4)
吴家湾金矿是汉阴北部地区的一个重要的金矿床,处于南秦岭石泉神河韧性滑脱逆冲推覆带。对其进行野外地质研究发现,吴家湾金矿赋矿层位为梅子垭组第一岩性段第四岩性层(S1m41),岩性主要为含碳绢云片岩夹硅质岩;控矿构造主要为RFa和RFb 2条顺层韧性剪切带,大致可分辨出S1、S2及S33期构造面理,S0几乎全部被置换,S2期变形与金矿成矿关系密切,金矿体主要于该期形成的韧性剪切带中产出。在地质研究基础上,可将吴家湾金矿区石英脉划分为3期,对流体包裹体的研究表明,包裹体类型以气液两相包裹体为主,纯气相、纯液相及三相包裹体较少见;均一温度范围介于176.8～344.4℃,集中于230～280℃。盐度范围为0.35%～13.51%,集中于2%～10%,成矿流体属于中低温、低盐度流体。流体捕获深度在1.38～3.47km,集中于1.5～2.8km,于中浅部成矿。S2期石英脉流与成矿关系紧密,流体包裹体均一温度主要集中在240～280℃,为主成矿期流体。激光拉曼光谱分析表明气液两相包裹体液相成分以H2O为主,含少量CO2和CH4;气相成分主要为CO2,其次为CH4、N2及H2S;包裹体类型主要为富含CO2的H2O CO2体系包裹体。对汉阴北部不同地区流体包裹体的性质进行对比研究后发现,流体包裹体均一温度为190～260℃,盐度为6%～10%,在这个区间内有利于成矿。 相似文献
3.
通过矿床流体包裹体岩相学、显微测温学和包裹体激光拉曼光谱分析研究成矿流体性质,探讨矿床成因类型。研究结果表明,流体包裹体有气液两相、含纯液相和纯气相包裹体3种类型。气相成分以CO2为主,其次为H2O,总体属CH4-H2O-CO2体系;结合氢氧同位素地球化学特征（δD值为-64.1‰～-124.4‰;δ18O值为1.34‰～-6.96‰）,确定成矿流体是岩浆热液与大气降水的混合流体。含矿硫（δ34S）指示硫主要为深部岩浆来源,并经历了陆壳硫的混染,包裹体均一温度以240℃～270℃区间为主,属中低温热液矿床。 相似文献
4.
山东玲珑金矿床成矿流体地球化学特征 总被引：3，自引：0，他引：3
玲珑金矿床第一成矿阶段与含金黄铁矿共生的石英中主要发育4种类型的原生流体包裹体:Ⅰ气液两相,Ⅱ含CO2三相,ⅢCO2,Ⅳ单液相包裹体。流体包裹体成分激光拉曼光谱分析及测温结果显示:①Ⅰa型包体,气液比10%~15%,均一温度为162.7~235.6℃,w(NaCl)(盐度)为4.65%~7.59%,气相平均摩尔分数为:H2O 96.48%,CO22.4%;②Ⅰb型包体,气液比30%~45%,均一温度266.9~349.2℃,w(NaCl)为10.8%~13.4%,气相平均摩尔分数为H2O 69.75%,CO224.74%;③Ⅱ型含CO2包体,CO2相所占比例为20%~90%,其均一温度为193.5~321.6℃,w(NaCl)2.9%~5.3%,CO2相中,H2O的摩尔分数为27.72%,CO2为70.6%。包裹体成分分析及测温结果综合研究认为,玲珑金矿成矿过程中存在大气降水热液与地幔来源流体的混合作用,前者与从流体中分离出的富CO2流体混合,以不同比例被捕获形成Ⅱ型包体;而与分异出CO2后的CO2不饱和地幔流体混合,被捕获形成Ⅰb型包体。两种流体混合导致的含矿热液物化条件变化对金的沉淀成矿具有重要意义。 相似文献
5.
甘肃花黑滩钼矿床位于北山造山带南带柳园地区,矿体产在花牛山碱长花岗岩与蓟县系平头山组接触带中。热液成矿过程包括早、晚两个阶段,矿物组合分别以石英-多金属硫化物和石英-(碳酸盐)-黄铁矿为标志,矿石矿物主要沉淀于早阶段。早阶段石英中发育富液二相包裹体、富气二相包裹体、含CO2三相包裹体和纯液相流体包裹体,均一温度范围为583~342℃,盐度范围为16.53%~15.67%NaCl,属高温、中等盐度流体。晚阶段石英中发育富液二相包裹体和纯液相流体包裹体,均一温度范围为306~142℃、盐度范围为15.66%~12.62%NaCl。从早阶段演化到晚阶段,流体温度显著降低,盐度变化不明显。矿石硫化物δ34S值大多为正值(1个样品为负值),范围集中于3.3‰~3.9‰,均一化程度较高,暗示矿石硫主要来自岩浆,有少量地层硫的贡献。围岩成矿元素分析表明,成矿物质主要源于花牛山碱长花岗岩。结合地质特征,认为该矿床属高温岩浆热液矿床,与花牛山碱长花岗岩成因联系密切。 相似文献
6.
桃行榴辉岩是苏鲁超高压变质带中段主要榴辉岩体密集分布区之一。流体包裹体研究表明,榴辉岩矿物及高压脉体石英中捕获有五种类型的流体包裹体：在超高压-高压榴辉岩相条件下捕获的N2±CH4包裹体;在榴辉岩发生麻粒岩相叠加变质作用期间被捕获的B型纯CO2液相包裹体;在高压榴辉岩重结晶阶段被捕获的C型CO2-H2O包裹体和D型高盐度水溶液包裹体;超高压岩石折返过程中的最晚阶段（角闪岩相退变质甚至更晚）捕获的E型低盐度水溶液包裹体。利用榴辉岩矿物及高压脉体石英中捕获的流体包裹体类型及期次可以重建超高压变质作用板片折返过程中的流体性状与演化,而石榴石中捕获的纯CO2包裹体为本区榴辉岩相岩石遭受了麻粒岩相叠加提供了佐证。 相似文献
7.
根据流体包裹体显微观察,均一温度、盐度测定和激光拉曼分析结果,毛坝气藏储层中存在多种类型包裹体,包括气液H20包裹体、烃一H20包裹体、气相烃包裹体、沥青包裹体和含自然硫气液H20包裹体。在含自然硫气液H20包裹体中,自然硫的特征激光拉曼峰值是151．1cm^1～、217．9em^1和473．3cm^1。根据包裹体的产状、分布以及组合特征,可将本区下三叠统储层流体包裹体划分为3期。晚成岩期方解石中气液H20包裹体均一温度变化范围为104～206°c,盐度为4．03％～19．29％NaCl。温度和盐度呈一定的负相关关系,反映随着成岩环境的埋藏深度增加,地层中孔隙水的温度趋于升高,同时烃类与流体中SO42发生热化学还原反应（TSR）,生成H2s和H20,使盐度降低。在区域抬升降温、降压期,由于外来流体的不均匀混合,流体温度、盐度进一步降低（均一温度为31～108℃,盐度为0．35％～4．03％NaCl）,在低温及硫主要以H2s形式存在的条件下,02与H2s反应生成大量自然硫。在自然硫形成过程中,随着温度的降低,pH值趋向于升高,lgf（02）趋向于降低。当温度为100℃时,自然硫在pH=2．9～3．4,lgf（02）=-50．61～-49．92的环境中形成;25℃时,自然硫形成于pH=1．9～6．5,lgf（02）=-69．30～-63．11的环境中。 相似文献
8.
新疆东准噶尔南明水金矿床位于卡拉麦里成矿带东段,矿体受NW—NWW向韧-脆性断裂控制,赋矿围岩为下石炭统姜巴斯套组的浅变质海相火山碎屑-沉积岩。以流体包裹体和氢、氧同位素为研究手段,查明了矿床成矿流体性质、来源及其演化特征与金成矿的关系。其热液成矿过程可划分早、中、晚3个阶段,石英中原生包裹体主要有CO2-H2O包裹体、水溶液包裹体和纯CO2包裹体3种类型。早阶段石英中以CO2-H2O包裹体和纯CO2包裹体为主,均一温度变化于257~339 ℃,盐度为04%~22%;中阶段石英中3种类型包裹体均发育,CO2-H2O包裹体和水溶液包裹体均一温度为196~361 ℃,盐度为04%~60%;晚阶段石英中仅见水溶液包裹体,均一温度相对较低,为174~252 ℃,盐度为14%~32%。由CO2-H2O包裹体计算的早、中阶段捕获压力分别为214~371 MPa、236~397 MPa,对应的成矿深度分别为81~140 km、89~150 km。成矿流体由早、中阶段的CO2-H2O-NaCl±CH4体系演化至晚阶段贫CO2的H2O-NaCl体系,成矿温度和流体密度呈逐渐降低趋势,盐度变化不大。流体包裹体和氢、氧同位素研究表明,主成矿阶段成矿流体主要来源于变质水,CO2-H2O-NaCl流体的不混溶是导致Au富集成矿的重要机制,南明水金矿属于中深成造山型金矿床。 相似文献
9.
张家口朱家洼钼矿床是近年来华北地台北缘中段继内蒙古曹四夭特大型钼矿床之后发现的又一个规模可达大型的钼矿床。钼矿床主要呈半隐伏—隐伏状围绕分布于骆驼山岩体周边。本次对矿区2个钻孔中采集的11件富含辉钼矿的石英矿物,进行了包裹体岩相学、显微测温、包裹体气、液相成分及氢氧分析。结果显示:该矿床流体包裹体可分为4种类型:富液相包裹体、富气相包裹体、含子晶包裹体和富CO2三相包裹体。其中,富CO2三相包裹体分布较少,其余3种类型包裹体常见。含子矿物的包裹体均一温度、盐度分别在400℃和45%NaCl eqv左右;富液相包裹体均一温度平均值为277.43℃,盐度20%NaCl eqv左右;富气包裹体和富CO2包裹体均一温度分别为380℃和30℃;盐度较低,分别为6%NaCl eqv和2.04%NaCl eqv左右。气液相成分分析显示流体体系成分以H2O、Cl-、F-、Na+、K+离子为主,Ca2+,SO42-含量较低,特征离子比值暗示流体来源于岩浆流体。成矿流体总体上属于H2O-NaCl体系。氢氧同位素组成显示,成矿流体主要来源于岩浆水。沸腾作用是辉钼矿沉淀的主要机制。 相似文献
10.
河北承德黑山铁矿床热液成矿特征及流体包裹体研究 总被引：3，自引：2，他引：1
黑山大型钒钛磁铁矿矿床产于大庙斜长岩杂岩体中,是承德地区最重要的"大庙式"岩浆型铁矿床。笔者在矿区野外地质观察过程中发现,穿插于斜长岩中的铁磷矿脉、磁铁矿硫化物矿脉有热液成矿作用的显示,表明黑山铁矿床成因除传统认为的岩浆期结晶、熔离、矿浆贯入成矿作用外,还有热液期的成矿作用发生。本文对热液成矿期铁磷矿石中磷灰石和矿化蚀变石英中的流体包裹体进行了显微测温和激光拉曼光谱分析。结果表明,磷灰石中原生包裹体可以分为气液两相包裹体、含子矿物包裹体、含液态CO2三相包裹体、单液相、单气相包裹体5类,均一温度主要集中于180～420℃,盐度主要集中于6.2%～38.9%NaCleq,流体包裹体气相成分主要为CO2、N2和CH4,液相成分主要为H2O,固相成分主要为方解石、石盐、白云石及铁氧化物子矿物。石英中流体包裹体类型和成分与磷灰石中的类似,但固相成分未发现石盐和不透明金属子矿物,均一温度变化于149～422℃,盐度变化于5.7%～22.9%NaCleq。成矿流体为CaCl2-NaCl-H2O-CO2体系,均一温度和盐度呈现正相关连续渐变的特征。铁磷矿石的磷灰石中原生包裹体为流体包裹体,盐度高,子矿物种类复杂,组成中富含CO2和CH4等,这些特征显示成矿流体以岩浆热液为主;成矿机理可能与大气降水对岩浆热液的稀释有关。 相似文献
11.
Most sulfide-rich magmatic Ni-Cu-(PGE) deposits form in dynamic magmatic systems by partial melting S-bearing wall rocks with variable degrees of assimilation of miscible silicate and volatile components, and generation of barren to weakly-mineralized immiscible Fe sulfide xenomelts into which Ni-Cu-Co-PGE partition from the magma. Some exceptionally-thick magmatic Cr deposits may form by partial melting oxide-bearing wall rocks with variable degrees of assimilation of the miscible silicate and volatile components, and generation of barren Fe ± Ti oxide xenocrysts into which Cr-Mg-V ± Ti partition from the magma. The products of these processes are variably preserved as skarns, residues, xenoliths, xenocrysts, xenomelts, and xenovolatiles, which play important to critical roles in ore genesis, transport, localization, and/or modification. Incorporation of barren xenoliths/autoliths may induce small amounts of sulfide/chromite to segregate, but incorporation of sulfide xenomelts or oxide xenocrysts with dynamic upgrading of metal tenors (PGE > Cu > Ni > Co and Cr > V > Ti, respectively) is required to make significant ore deposits. Silicate xenomelts are only rarely preserved, but will be variably depleted in chalcophile and ferrous metals. Less dense felsic xenoliths may aid upward sulfide transport by increasing the effective viscosity and decreasing the bulk density of the magma. Denser mafic or metamorphosed xenoliths may also increase the effective viscosity of the magma, but may aid downward sulfide transport by increasing the bulk density of the magma. Sulfide wets olivine, so olivine xenocrysts may act as filter beds to collect advected finely dispersed sulfide droplets, but other silicates and xenoliths may not be wetted by sulfides. Xenovolatiles may retard settling of – or in some cases float – dense sulfide droplets. Reactions of sulfide melts with felsic country rocks may generate Fe-rich skarns that may allow sulfide melts to fractionate to more extreme Cu-Ni-rich compositions. Xenoliths, xenocrysts, xenomelts, and xenovolatiles are more likely to be preserved in cooler basaltic magmas than in hotter komatiitic magmas, and are more likely to be preserved in less dynamic (less turbulent) systems/domain/phases than in more dynamic (more turbulent) systems/domains/phases. Massive to semi-massive Ni-Cu-PGE and Cr mineralization and xenoliths are often localized within footwall embayments, dilations/jogs in dikes, throats of magma conduits, and the horizontal segments of dike-chonolith and dike-sill complexes, which represent fluid dynamic traps for both ascending and descending sulfides/oxides. If skarns, residues, xenoliths, xenocrysts, xenomelts, and/or xenovolatiles are present, they provide important constraints on ore genesis and they are valuable exploration indicators, but they must be included in elemental and isotopic mass balance calculations. 相似文献
12.
针对兖州煤田下组煤深部开采受奥灰高承压水威胁以及当地大型煤化工企业生产用水量大的现状,在已进行的水文地质勘探及放水试验基础上,评价奥灰富水性,并采用有限差分法进行奥灰疏水降压数值模拟研究,提出水煤共采观点。研究结果表明:兖州煤田深部奥灰水压高,合理布置水煤共采孔,可以实现奥灰水位的有效疏降,疏降中心区水位最大降深可达110 m,突水系数显著下降,提高了下组煤开采的安全性;同时可提供煤化工43200 m3/d的供水量,能达到可持续的、水资源保护性的供水效果,实现下组煤的水煤共采。 相似文献
13.
《Chemical Geology》2007,236(1-2):13-26
We examined the coprecipitation behavior of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides under two different fluoride forming conditions: at < 70 °C in an ultrasonic bath (denoted as the ultrasonic method) and at 245 °C using a Teflon bomb (denoted as the bomb method). In the ultrasonic method, small amounts of Ti, Mo and Sn coprecipitation were observed with 100% Ca and 100% Mg fluorides. No coprecipitation of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides occurred when the sample was decomposed by the bomb method except for 100% Ca fluoride. Based on our coprecipitation observations, we have developed a simultaneous determination method for B, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by Q-pole type ICP-MS (ICP-QMS) and sector field type ICP-MS (ICP-SFMS). 9–50 mg of samples with Zr–Mo–Sn–Sb–Hf spikes were decomposed by HF using the bomb method and the ultrasonic method with B spike. The sample was then evaporated and re-dissolved into 0.5 mol l− 1 HF, followed by the removal of fluorides by centrifuging. B, Zr, Mo, Sn, Sb and Hf were measured by ID method. Nb and Ta were measured by the ID-internal standardization method, based on Nb/Mo and Ta/Mo ratios using ICP-QMS, for which pseudo-FI was developed and applied. When 100% recovery yields of Zr and Hf are expected, Nb/Zr and Ta/Hf ratios may also be used. Ti was determined by the ID-internal standardization method, based on the Ti/Nb ratio from ICP-SFMS. Only 0.053 ml sample solution was required for measurement of all 9 elements. Dilution factors of ≤ 340 were aspirated without matrix effects. To demonstrate the applicability of our method, 4 carbonaceous chondrites (Ivuna, Orgueil, Cold Bokkeveld and Allende) as well as GSJ and USGS silicate reference materials of basalts, andesites and peridotites were analyzed. Our analytical results are consistent with previous studies, and the mean reproducibility of each element is 1.0–4.6% for basalts and andesites, and 6.7–11% for peridotites except for TiO2. 相似文献
14.
Hirokazu Fujimaki 《Contributions to Mineralogy and Petrology》1986,94(1):42-45
Concentration ratios of Hf, Zr, and REE between zircon, apatite, and liquid were determined for three igneous compositions: two andesites and a diorite. The concentration ratios of these elements between zircon and corresponding liquid can approximate the partition coefficient. Although the concentration ratios between apatite and andesite groundmass can be considered as partition coefficients, those for the apatite in the diorite may deviate from the partition coefficients. The HREE partition coefficients between zircon and liquid are very large (100 for Er to 500 for Lu), and the Hf partition coefficient is even larger. The REE partition coefficients between apatite and liquid are convex upward, and large (D=10–100), whereas the Hf and Zr partition coefficients are less than 1. The large differences between partition coefficients of Lu and Hf for zircon-liquid and for apatite-liquid are confirmed. These partition coefficients are useful for petrogenetic models involving zircon and apatite. 相似文献
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17.
The distribution of Cu, Co, As and Fe was studied downstream from mines and deposits in the Idaho Cobalt Belt (ICB), the largest Co resource in the USA. To evaluate potential contamination in ecosystems in the ICB, mine waste, stream sediment, soil, and water were collected and analyzed for Cu, Co, As and Fe in this area. Concentrations of Cu in mine waste and stream sediment collected proximal to mines in the ICB ranged from 390 to 19,000 μg/g, exceeding the USEPA target clean-up level and the probable effect concentration (PEC) for Cu of 149 μg/g in sediment; PEC is the concentration above which harmful effects are likely in sediment dwelling organisms. In addition concentrations of Cu in mine runoff and stream water collected proximal to mines were highly elevated in the ICB and exceeded the USEPA chronic criterion for aquatic organisms of 6.3 μg/L (at a water hardness of 50 mg/L) and an LC50 concentration for rainbow trout of 14 μg/L for Cu in water. Concentrations of Co in mine waste and stream sediment collected proximal to mines varied from 14 to 7400 μg/g and were highly elevated above regional background concentrations, and generally exceeded the USEPA target clean-up level of 80 μg/g for Co in sediment. Concentrations of Co in water were as high as in 75,000 μg/L in the ICB, exceeding an LC50 of 346 μg/L for rainbow trout for Co in water by as much as two orders of magnitude, likely indicating an adverse effect on trout. Mine waste and stream sediment collected in the ICB also contained highly elevated As concentrations that varied from 26 to 17,000 μg/g, most of which exceeded the PEC of 33 μg/g and the USEPA target clean-up level of 35 μg/g for As in sediment. Conversely, most water samples had As concentrations that were below the 150 μg/L chronic criterion for protection of aquatic organisms and the USEPA target clean-up level of 14 μg/L. There is abundant Fe oxide in streams in the ICB and several samples of mine runoff and stream water exceeded the chronic criterion for protection of aquatic organisms of 1000 μg/L for Fe. There has been extensive remediation of mined areas in the ICB, but because some mine waste remaining in the area contains highly elevated Cu, Co, As and Fe, inhalation or ingestion of mine waste particulates may lead to human exposure to these elements. 相似文献
18.
E. M. Prasolov S. A. Sergeev B. V. Belyatsky E. S. Bogomolov K. A. Gruzdov I. N. Kapitonov R. Sh. Krymsky V. O. Khalenev 《Geochemistry International》2018,56(1):46-64
This paper reports the first results of a study of 11 isotope systems (3He/4He, 40Ar/36Ar, 34S/32S, 65Cu/63Cu, 62Ni/60Ni, 87Sr/86Sr, 143Nd/144Nd, 206–208Pb/204Pb, Hf–Nd, U–Pb, and Re–Os) in the rocks and ores of the Cu–Ni–PGE deposits of the Norilsk ore district. Almost all the results were obtained at the Center of Isotopic Research of the Karpinskii All-Russia Research Institute of Geology. The use of a number of independent genetic isotopic signatures and comprehensive isotopic knowledge provided a methodic basis for the interpretation of approximately 5000 isotopic analyses of various elements. The presence of materials from two sources, crust and mantle, was detected in the composition of the rocks and ores. The contribution of the crustal source is especially significant in the paleofluids (gas–liquid microinclusions) of the ore-forming medium. Crustal solutions were probably a transport medium during ore formation. Air argon is dominant in the ores, which indicates a connection between the paleofluids and the atmosphere. This suggests intense groundwater circulation during the crystallization of ore minerals. The age of the rocks and ores of the Norilsk deposits was determined. The stage of orebody formation is restricted to a narrow age interval of 250 ± 10 Ma. An isotopic criterion was proposed for the ore-bearing potential of mafic intrusions in the Norilsk–Taimyr region. It includes several interrelated isotopic ratios of various elements: He, Ar, S, and others. 相似文献
19.
The dielectric constants and dielectric loss values of 4 Ca-containing minerals were determined at 1 MHz using a two-terminal method and empirically determined edge corrections. The results are: vesuvianitel κ′ a=9.93 tan δ=0.006 κ′ c=9.79 tan δ=0.005 vesuvianitel κ′ a=10.02 tan δ=0.002 κ′ c=9.85 tan δ=0.003 zoisite1 κ′ a =10.49 tan δ=0.0006 κ′ b =15.31 tan δ=0.0008 κ′ c=9.51 tan δ=0.0008 zoisite2 κ′ a =10.55 tan δ=0.0011 κ′ b =15.45 tan δ=0.0013 κ′ c=9.39 tan δ=0.0008 epidote κ′ 11= 9.52 tan δ=0.0008 κ′ 22=17.1 tan δ=0.0009 κ′ 33= 9.37 tan δ=0.0006 fluorapatite1 κ′ a =10.48 tan δ=0.0008 κ′ c = 8.72 tan δ=0.0114 fluorapatite2 κ′ a =10.40 tan δ=0.0010 κ′ c=8.26 tan δ=0.0178 The deviation (δ) between measured dielectric polarizabilities as determined from the Clausius-Mosotti equation and those calculated from the sum of oxide polarizabilities according to α D (mineral)=∑ α D (oxides) for vesuvianite is ～ 0.5%. The large deviations of epidote and zoisite from the additivity rule with Δ=+ 10.1 and + 11.7%, respectively, are attributed to “rattling” Ca ions. The combined effects of both a large F thermal parameter and possible F-ion conductivity in fluorapatite are believed to be responsible for Δ=+2–3%. Although variation of oxygen polarizability with oxygen molar volume (Vo) is believed to affect the total polarizabilities, the variation of Vo in these Ca minerals is too small to observe the effect. 相似文献
20.
Geochemistry and petrology of selected coal samples from Sumatra, Kalimantan, Sulawesi, and Papua, Indonesia 总被引：4，自引：1，他引：3
Harvey E. Belkin Susan J. Tewalt James C. Hower J.D. Stucker J.M.K. O'Keefe 《International Journal of Coal Geology》2009,77(3-4):260-268
Indonesia has become the world's largest exporter of thermal coal and is a major supplier to the Asian coal market, particularly as the People's Republic of China is now (2007) and perhaps may remain a net importer of coal. Indonesia has had a long history of coal production, mainly in Sumatra and Kalimantan, but only in the last two decades have government and commercial forces resulted in a remarkable coal boom. A recent assessment of Indonesian coal-bed methane (CBM) potential has motivated active CBM exploration. Most of the coal is Paleogene and Neogene, low to moderate rank and has low ash yield and sulfur (generally < 10 and < 1 wt.%, respectively). Active tectonic and igneous activity has resulted in significant rank increase in some coal basins. Eight coal samples are described that represent the major export and/or resource potential of Sumatra, Kalimantan, Sulawesi, and Papua. Detailed geochemistry, including proximate and ultimate analysis, sulfur forms, and major, minor, and trace element determinations are presented. Organic petrology and vitrinite reflectance data reflect various precursor flora assemblages and rank variations, including sample composites from active igneous and tectonic areas. A comparison of Hazardous Air Pollutants (HAPs) elements abundance with world and US averages show that the Indonesian coals have low combustion pollution potential. 相似文献