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1.
新疆巴尔鲁克地区石屋岩体主要由石英闪长玢岩、石英闪长岩组成。本文通过锆石U-Pb年代学、岩石地球化学和Sr-Nd-Pb-Hf同位素等研究,探讨其构造背景、岩石成因和成矿意义。LA-ICP-MS锆石U-Pb定年表明:石屋石英闪长玢岩的成岩年龄为322.1±1.5Ma,石英闪长岩的形成年龄为322.4±1.5Ma,二者形成时代为晚石炭世。石屋石英闪长玢岩和石英闪长岩地球化学特征相似,Mg~#为32.4~57.2,轻重稀土分馏较明显且富集轻稀土((La/Yb)N=2.36~6.04),Eu异常不明显,相对富集LILEs等,亏损Nb、Ta、P、Ti等高场强元素。Sr-Nd-Pb-Hf同位素显示:样品具有低的ISr值(0.7036~0.7045),正εNd(t)值(+4.61~+7.03),年轻的tDM1年龄(0.59~0.78Ga),初始铅同位素比值为(~(206)Pb/~(204)Pb)i=18.173~18.450,(~(207)Pb/~(204)Pb)i=15.542~15.562,(~(208)Pb/~(204)Pb)i=37.830~38.036,锆石εHf(t)值为+4.5~+15.3,t_(DM2)=0.36~0.62Ga。综合石屋岩体的地质、地球化学和年代学特征,认为石英闪长玢岩和石英闪长岩源区相同,它们均形成于晚石炭世早期俯冲背景下的岛弧环境,可能是在亏损玄武质岩浆(俯冲板片脱水交代地幔楔产生的上涌岩浆)底侵作用下,新生地壳发生部分熔融,并有部分玄武质岩浆加入,发生混合、侵位的产物。石屋岩体的形成环境及其岩浆演化过程可能有利于区内斑岩型铜矿化,其含矿性值得做进一步评价。  相似文献   

2.
文章对东天山玉海铜钼矿区含矿岩体石英闪长(玢)岩及围岩二长花岗岩的成岩年龄进行研究。LAMC-ICP-MS锆石U-Pb定年结果显示石英闪长(玢)岩形成于(427.80±0.98)Ma,即中志留世;二长花岗岩形成于(318.40±0.66)Ma,即晚石炭世。石英闪长(玢)岩w(SiO_2)为58.30%~64.28%,w(Al2O3)为15.24%~17.36%,w(MgO)为1.73%~4.80%,w(Y)为10.20×10~(-6)~17.40×10~(-6),w(Yb)为1.33×10~(-6)~1.98×10~(-6),石英闪长(玢)岩Sr/Y比值为41.58~79.22,(La/Yb)N为4.19~10.04,为类埃达克岩(adakite-like)。石英闪长(玢)岩具轻稀土元素富集、重稀土元素亏损的配分型式,Eu无异常或正异常,富集大离子亲石元素,亏损高场强元素,具有典型岛弧岩浆岩的特征。Sr-Nd同位素(εNd(t)=+5.4~+7.1,(87Sr/86Sr)i=0.703 59~0.703 83)表明其源区是亏损地幔。通过与土屋-延东斑岩矿床含矿岩体的对比研究,认为玉海石英闪长(玢)岩也形成于岛弧环境,但源区可能是俯冲流体改造过的地幔楔。综合区域早古生代岩浆岩的资料,认为大南湖-头苏泉岛弧带早古生代为不成熟弧环境,与准噶尔洋向南俯冲有关。  相似文献   

3.
延边小西南岔金铜矿区早白垩世英云闪长岩的岩石成因   总被引：3，自引：0，他引：3  
李红霞  郭锋  李超文  赵亮 《地球化学》2012,41(6):497-514
锆石U-Pb测年结果表明小西南岔富金铜矿床矿区内的英云闪长岩形成于(112±1)Ma。该英云闪长岩富Na2O和Al2O3,高Sr、LREE(轻稀土元素),低Y、Yb和HREE(重稀土元素)(如Sr=369~774μg/g,(La/Yb)CN=7.5~17.5),具有类似于埃达克质岩石的元素地球化学特征。在同位素组成上具中等放射成因Sr((87Sr/86Sr)i=0.7044~0.7048)、Nd(εNd(t)=+0.5~+1.7)和Hf(εHf(t)=+5.4~+8.6,ΔεHf=2.3~4.2)同位素,高放射成因Pb((206Pb/204Pb)i=18.40~18.60;(207Pb/204Pb)i=15.56~18.60;(208Pb/204Pb)i=38.22~38.36)同位素的特点。结合区域构造背景以及古太平洋板块俯冲历史,笔者倾向认为该岩体可能是玄武质岩浆底侵下地壳部分熔融形成的,而非板片熔融形成的埃达克质岩浆,岩浆源区为石榴子石角闪岩相向角闪岩相过渡的岩石。该岩体侵位的晚古生代((257±3)Ma)镁铁质围岩的角闪石Ar-Ar坪年龄为(110.1±1.5)Ma,与英云闪长岩的侵位时间一致,暗示晚古生代镁铁质侵入岩经历的热液事件与英云闪长岩的侵位作用存在成因联系,区域金铜矿化可能为早白垩世岩浆热液作用下成矿物质富集而形成。  相似文献   

4.
新疆东天山黄山岩体岩石地球化学特征与岩石成因   总被引：1，自引：0，他引：1  
黄山岩体位于东天山北部的土墩-黄山-图拉尔根镁铁-超镁铁质岩带中段,受康古尔塔格-黄山韧性剪切带控制,主要由橄榄岩、橄榄二辉岩、辉石岩、辉长苏长岩、辉长岩以及辉长闪长岩组成.岩石化学组成属拉斑玄武岩系列,普遍富集大离子亲石元素(Rb,Ba,Sr),亏损高场强元素(Nb,Ta,Ti).岩体εNd(t)=+4.1～+9.2,除3件样品εSr(t)为+2.2,+12.5和+15.4,大部分εSr(t)=(-22.5～-4.5),Nd,Sr同位素组成基本属亏损型地幔特征;Pb同住素初始值(206Pb/204Pb)i=18.081～18.413,(207Pb/204Pb)i=15.441～15.513,(208Pb/204Pb)i=37.461 6～37.899,具有MORB亲和性.岩相学及岩石地球化学特征显示岩浆演化过程中主要发生了橄榄石、斜方辉石、单斜辉石和斜长石的分离结晶作用.岩浆演化晚期阶段发生了一定程度的同化混染作用,元素地球化学和Nd,Sr,Pb同位素体系证明,岩浆源区主体由软流圈地幔物质组成,同时也有一定量富集型岩石圈地幔组份加入.黄山岩体是岩石圈根部拆沉加热熔融和软流圈地幔上涌减压熔融的产物,这种地幔动力学机制应该对应于后碰撞伸展环境.  相似文献   

5.
蒙西斑岩铜钼矿含矿斑岩体主要为斜长花岗斑岩。通过对含矿斑岩体地球化学和Sr-Nd-Pb同位素特征的研究,确立斑岩体为过铝质钙碱性系列岩石,富集Rb,Ba,U,K,Pb,Sr等大离子亲石元素,亏损Th,Ta,Nb,Nd,Ti等高场强元素;具低的(87Sr/86Sr)ⅰ值(0.704 65~0.705 37)和相对较高的εNd(t)值(-2.2~6.6),且有较低的初始铅同位素比值(206Pb/204Pb)i=17.13~17.33,(207Pb/204Pb)i=15.47~15.54,(208Pb/204Pb)i=37.11~37.33。上述特征表明其形成于岛弧环境,岩浆物质来源以幔源为主,但也有少量壳源组分参与,岩浆的形成可能与洋壳的俯冲作用有关。东准噶尔琼河坝地区是形成和寻找斑岩型铜矿的有利地区。  相似文献   

6.
山东邹平青山下亚组玄武安山岩源区性质及成因   总被引：1，自引：0，他引：1  
本文通过岩石的显微观察、全岩元素地球化学及Sr-Nd-Pb同位素组成等综合研究,参照前人的研究成果,探讨邹平火山岩盆地内青山下亚组玄武安山岩的岩石地球化学性质、物质来源及岩石成因。研究表明,岩石富钠、富镁,具有大离子亲石元素(Rb、Sr、Ba)和轻稀土元素(LREE)富集,高场强元素(Nb、Ta、Ti)相对亏损的地球化学特征。全岩Sr同位素初始比值(87 Sr/86 Sr)i为0.705674~0.705876;全岩Nd同位素初始比值εNd(t)为-10.0~-10.2,Nd同位素二阶段模式年龄T2DM为1.74~1.75Ga;全岩铅同位素初始比值(206Pb/204Pb)i介于16.917~17.095之间,(207Pb/204Pb)i介于15.306~15.396之间,(208Pb/204Pb)i介于36.750~37.208之间;较低的Sr-Nd初始比值及较均一的低放射性铅同位素组成,可能为EMI型富集地幔的部分熔融所致。晚中生代加厚的华北岩石圈发生大规模拆沉作用,拆沉的大陆中下地壳部分熔融形成富硅熔体与古生代岩石圈地幔相互作用形成富集地幔,随后在岩石圈伸展与区域热异常作用下减压部分熔融,形成的玄武安山质岩浆沿着深大构造侵入地壳上部或喷发至地表,形成青山下亚组玄武安山岩,但是岩浆上侵过程中地壳物质混染不强。该研究对深化鲁西地区晚中生代构造-岩浆作用的认识有一定的理论意义。  相似文献   

7.
本文对新县花岗岩岩基进行了系统的锆石U-Pb定年,全岩元素地球化学、Sr-Nd-Pb-Hf同位素测试,研究探讨其成岩年龄、岩石成因、物质来源以及地球化学动力学背景。锆石U-Pb年龄为125.5±1.5Ma,属于早白垩世产物。全岩元素地球化学成分表现为高硅、富碱,贫镁、铁和钙,富集轻稀土元素、大离子亲石元素（Rb、K、Th、U）和Pb,亏损重稀土元素、高场强元素(Nb、Ta、Ti)和Sr、Ba。全岩同位素具有中等略偏高的Sr 初始比值(87Sr/86Sr)i=0.706949~0.707086;低的放射性Pb同位素组成[ (206Pb/204Pb)i=16.611～17.152,(207Pb/204Pb)i=15.304～15.432,(208Pb/204Pb)i=37.316～37.702]; 低的Nd初始比值（εNd(t)=-13.65～-13.51）和老的Nd模式年龄（TDM2=2.12～2.13Ga）。锆石原位Hf同位素具有较低的初始比值（εHf(t)=-22.92～-19.40）和老的Hf二阶段模式年龄（TDM2=2.39~2.61 Ga）。综合以上元素地球化学特征、锆石U-Pb定年结果及Sr-Nd-Pb-Hf同位素组成,新县花岗岩岩基应属于分异的高钾钙碱性I型花岗岩,是化学成分类似于扬子板块北缘新元古代TTG型岩浆岩的扬子下地壳在非加厚下地壳（深度小于35km）环境下部分熔融的产物。  相似文献   

8.
广西横县马山杂岩体位于钦杭成矿带西南段,出露于防城—灵山断裂带的西侧,为一套包括辉长岩、玄武(玢)岩、闪长(玢)岩、二长(斑)岩、普通角闪正长岩、石英正长岩、花岗岩在内的从基性到中、酸性的岩浆岩岩系。文中对其中的中性浅成侵入岩进行研究,获得二长闪长玢岩样品的40Ar/39Ar坪年龄为(153.8±0.6)Ma,表明岩石形成于晚侏罗世。所研究的岩石样品富K、富碱、w(K2O+Na2O)=5.73%~8.54%、K2O/Na2O=0.87~1.76,富集大离子亲石元素Rb、Ba、Th、U和轻稀土元素,无明显的Nb-Ta-Ti负异常,为典型板内钾玄质岩石。其(87Sr/86Sr)i变化范围在0.705 11~0.705 47,εNd(t)变化范围在0.6~1.4,206Pb/204Pb为19.019~19.228,207Pb/204Pb为15.720~15.737,208Pb/204Pb为39.372~39.518,元素和同位素地球化学特征指示岩浆来源于亏损的软流圈地幔(DMM)和富集岩石圈地幔(EMⅡ)两个端员的混合。结合前人对南岭西部侏罗纪岩浆岩的研究成果,认为马山杂岩体的岩浆成分和源区特征反映桂东南在晚侏罗世发生了区域软流圈地幔上涌和岩石圈伸展-减薄作用,这是钦杭带西南段燕山期花岗岩和相关矿床形成的重要的地质构造背景。  相似文献   

9.
对辽东卧龙泉黑云二长花岗岩进行锆石U-Pb定年、岩石地球化学和Sr-Nd-Pb同位素研究,以探讨岩石成因及动力学意义。LA-ICPMS锆石U-Pb定年结果显示卧龙泉岩体侵位时代为早侏罗世(194.0±1.0Ma,MSWD=1.3)。岩石地球化学特征显示,岩石具有高硅(71.49%~72.24%)、富碱(7.58%~7.83%)、贫镁(0.454%~0.497%)特点,属于高钾钙碱性系列,A/CNK值介于1.07~1.10之间,属于弱过铝质I型花岗岩,岩石富集大离子亲石元素(如K、Rb)和轻稀土元素(LREE),亏损高场强元素(如Nb、Ta、P、Ti)。同位素方面,岩石具有高的(87 Sr/86 Sr)i比值(0.71309~0.71410)和低的εNd(t)值(-15.6~-17.6);Pb同位素组成相对均一,(206Pb/204Pb)t为17.751~17.825,(207Pb/204Pb)t为15.542~15.557,(208 Pb/204 Pb)t为38.888~39.203;Sr-Nd-Pb同位素和岩石地球化学表明,卧龙泉岩体由俯冲作用引起的加厚地壳部分熔融形成。结合区域构造演化,认为卧龙泉岩体乃至华北东部侏罗纪花岗质岩浆作用可能形成于古太平洋板块向欧亚大陆俯冲、陆壳挤压和华北板块与西伯利亚板块南北挤压碰撞双重构造环境。  相似文献   

10.
琼河坝矿集区花岗岩体的Sr-Nd,Pb同位素特征及地质意义   总被引：1，自引：0，他引：1  
琼河坝地区在志留纪—泥盆纪频繁的岩浆活动与成矿关系密切。矿集区中花岗岩ΣREE含量23.16×10-6~110.24×10-6,平均值68.19×10-6,总体上稀土含量较低。(La/Yb)N=3.23~10.97平均值为5.74,显示轻、重稀土分馏不明显,且轻稀土元素较重稀土元素富集。蒙西、琼河坝、和尔赛三个花岗岩体Sr-Nd、Pb同位素值很近,表明琼河坝花岗岩具有相近的成因。(87Sr/86Sr)i值为0.704 01~0.704 42,平均值为0.704 19;(143 Nd/144 Nd)i值为0.512 300~0.512 478,平均值为0.512 415;(208Pb/204Pb)i值17.600~17.910,平均值为17.738,(207Pb/204Pb)i值为15.410~15.547,平均值为15.459,(206Pb/204Pb)i值为37.250~38.019平均值为37.534。表现出壳幔混染的特征。εSr(t)值为-0.3~7.8,εNd(t)值为2.9~7.2,为较小的正值,表现出洋壳的特征。花岗岩Al2O3,Sr,Y,Yb和δEu的特征与埃达克岩相近,可能为俯冲洋壳熔融的产物。因此该地区众多铜矿点的出现,应该与埃达克岩有关。  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.
Partition coefficients of Hf,Zr, and REE between zircon,apatite, and liquid   总被引：25，自引：2，他引：25  
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   

14.
《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   

15.
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16.
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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.
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   

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.
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   

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