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1.
The elemental composition of high temperature ash (750°C) and forms of S were studied in 25 coal seams from the Escucha Formation (Middle Albian) in the Teruel Mining District, northeast Spain. The principal analytical method was ICP-MS, but ICP-ES was also used in the determination of some trace elements. The analytical data show wide ranges of trace element cotnents among the coal seams studied, even in the vertical profile of a single coal seam. These wide ranges of the trace element concentrations are attributed to both syngenetic and epigenetic processes.When a comparison was made between the average trace element contents of the Teruel Mining District coals, and those of the average content in worldwide coals, the Teruel coals show slightly higher concentrations of Be and U, and lower concentrations of Ba, Cd, Mn, Pb, Sr and Zr. Further, three main groups of trace elements were differentiated on the basis of the inorganic/organic association: (1) trace elements with inorganic affinity; Ba, Ce, Co, Cr, La, Mn, Ni, Rb and Zr. Between these, Ba, Ce, Cr and Rb show a well defined correlation with the clay mineral content, and Co and Ni with pyritic-S content; (2) trace elements with an intermediate (mixed) affinity; As, Cd, Cu, Dy, Er, Eu, Gd, Ge, Ho, Lu, Mo, Nd, Pb, Pr, Sb, Sm, Sr, Tb, Th, Tm, U, Yb and Zn. In this group, As, Cd, Cu, Ge, Mo, Th, U and Zn show a weak trend associated with the mineral matter and Sr with the organic matter; and (3) Be shows an organic affinity. The high mineral matter content (21.3% HTA) of the Teruel coals may account for the great number of elements with inorganic affinity. This classification represents a general trend, but the results show that the affinities of some trace elements (e.g. As, Sb and Zn) may vary from one coal seam to another in the Teruel Mining District. 相似文献
2.
The mineral and inorganic chemical composition of five types of samples from the Pernik subbituminous coals and their products generated from the Pernik preparation plant were studied. They include feed coal, low-grade coal, high-grade coal, coal slime, and host rock. The mineral matter of the coals contains 44 species that belong mainly to silicates, carbonates, sulphates, sulphides, and oxides/hydroxides, and to a lesser extent, chlorides, biogenic minerals, and organic minerals. The detrital minerals are quartz, kaolinite, micas, feldspars, magnetite, cristobalite, spessartine, and amphibole. The authigenic minerals include various sulphides, silicates, oxihydroxides, sulphates, and carbonates. Several stages and substages of formation were identified during the syngenetic and epigenetic mineral precipitations of these coals. The authigenic minerals show the greatest diversity of mineral species as the epigenetic mineralization (mostly sulphides, carbonates, and sulphates) dominates qualitatively and quantitatively. The epigenetic mineralization was a result of complex processes occurring mostly during the late development of the Pernik basin. These processes indicate intensive tectonic, hydrothermal and volcanic activities accompanied by a change from fresh to marine sedimentation environment. Thermally altered organic matter due to some of the above processes was also identified in the basin. Most of the trace elements in the Pernik coals (Mo, Be, S, Zr, Y, Cl, Ba, Sc, Ga, Ag, V, P, Br, Ni, Co, Pb, Ca, and Ti) show an affinity to OM and phases intimately associated with OM. Some of the trace elements (Sr, Ti, Mn, Ba, Pb, Cu, Zn, Co, Cr, Ni, As, Ag, Yb, Sn, Ga, Ge, etc.) are impurities in authigenic and accessory minerals, while other trace elements (La, Ba, Cu, Ce, Sb, Bi, Zn, Pb, Cd, Nd, etc.) occur as discrete phases. Elements such as Sc, Be, Y, Ba, V, Zr, S, Mo, Ti, and Ga exceed Clarke concentrations in all of the coal types studied. It was also found that a number of elements in the Pernik coals (F, V, As, Pb, Mo, Li, Sr, Ti, Ga, Ni, Ge, Cr, Mn, etc.) reveal mobility in water and could have some environmental concerns. 相似文献
3.
The ash yield and concentrations of twenty-four minor and trace elements, including twelve potentially hazardous trace elements were determined in Mukah coal from Sarawak, Malaysia. Comparisons made to the Clarke values show that Mukah coal is depleted in Ag, Ba, Be, Cd, Co, Mn, Ni, Se, U, and V. On the other hand, it is enriched in As, Cr, Cu, Pb, Sb, Th, and Zn. Among the trace elements studied, V and Ba are associated predominantly with the clay minerals. Manganese, Cr, Cu, Th, and Ni are mostly bound within the aluminosilicate, sulphide and/or carbonate minerals in varying proportions, though a portion of these elements are also organically bound. Arsenic, Pb and Sb are mostly organically bound, though some of these elements are also associated with the sulphide minerals. Zinc is associated with both the organic and inorganic contents of the coal. Among the potentially hazardous trace elements, Be, Cd, Co, Mn, Ni, Se, and U may be of little or no health and environmental concerns, whereas As, Cr, Pb, Sb and Th require further examination for their potential health and environmental concerns. Of particular concern are the elements As, Pb and Sb, which are mostly organically bound and hence cannot be removed by physical cleaning technologies. They escape during coal combustion, either released as vapours to the atmosphere or are adsorbed onto the fine fly ash particles. 相似文献
4.
用质子探针和电子探针分别测定盘石山幔源橄揽岩包体中透辉石、橄榄石的微量元素和主量元素丰度;用X-射线荧光光谱法测定包体全岩的主量和微量元素丰度。定量讨论微量元素的分布和分配。其中绝大部分Sr、Zr、Ti、Na赋存在透辉石中,绝大部分Mn、Zn、Ni赋存在橄揽石中,在T=1194-1435K范围,分配系数变化如下:InDOl/CpxZn=1.44-2.19;InDOl/CpxMn=0.21-0.40,InDOl/CpxTi=4.76-5.61,InDOl/CpxNi(平均值)=2.20.透辉石中Ti/Zr=42-103,低于原始地幔值,由地幔隐性交代作用造成。 相似文献
5.
A method is presented for the determination of 15 trace and minor elements (Fe, Ti, V, Cr, Mn, Ni, Cu, Zn, Pb, Sr, Rb, Ba, Zr, Y, Nb) in whole coal, by X-ray fluorescence spectrometry. A Rhanode X-ray tube is used and matrix corrections are derived from the intensity of the rhodium Kα Compton scattered tube line. The calibration is based on synthetic coals made from mixtures of standard rocks with graphite and cellulose, emulating the range of compositions likely to be encountered in bituminous coals. Robust pellets are made from 9 g of coal blended with a powdered binder. Results are presented for a number of standard coals. 相似文献
6.
吉林白山地区原煤微量元素地球化学特征 总被引：2，自引：1，他引：1
对吉林白山地区煤矿主采煤层中的As、B、Ba、Cd、Cu、Hg、Pb、Se、Sr等微量元素进行了分析,结果表明:太原组与山西组由于成煤环境不同,微量元素组成及其质量分数存在一定的差异,太原组原煤中As、B、Hg、Pb、Se、Zn的质量分数明显高于山西组,山西组原煤中Ba、Cr、Cu、Mn、V的质量分数明显高于太原组。白山地区原煤中As、B、Hg、Pb、Se的质量分数明显高于地壳元素平均值,呈富集状态;Co、Cd与地壳平均值接近,其他元素均亏损。与全国煤中微量元素的质量分数平均值相比,As、Ba、Co、Cr、Cu、Hg、Ni、Pb、Se、V、Zn的质量分数高于全国平均值。B、Mn、Sr质量分数低于全国平均值。微量元素赋存状态及相关分析表明,Fe与亲硫有害元素As、Cu、Hg、Pb、Se具有显著相关关系,说明煤中黄铁矿及其他硫化物是许多有害微量元素的重要载体。 相似文献
7.
陕西渭北聚煤区原煤的微量元素组成特征 总被引：4，自引：0，他引：4
对陕西省渭北主要煤田主采煤层中的As、Pb、Hg、Cd、Se、Cu、Sr、Ba、B等微量元素的分析结果表明：渭北原煤中Hg、Se、As、Pb、B含量明显高于地壳平均值，呈富集状态；Co、Cd与地壳平均值接近，Cu、Zn、Sr、Ba等元素均亏损。太原组和山西组由于成煤环境不同，煤质和原煤的微量元素组成特征存在一定的差异。太原组煤的友分和硫分均较山西组煤高，原煤中As、Hg、Se、Pb、Zn、B的合量明显高于山西组原煤，而山西组原煤中V、Cr、Cu、Mn、Ba的含量别明显高于大原组原煤。统计分析表明，As、Hg、Se、Pb、Cu等亲硫元素与铁呈显著的正相关关系，它们的赋存形式可能与煤中黄铁矿有关。 相似文献
8.
Trace-element data are presented for the first time for any coal seam in India, across a full working section, based on systematically collected channel samples of coal, together with their maceral composition. The trace-element variation curves along the seam profile are presented together with group maceral compositions of Kargali Bottom, Kargali Top, Kargali, Kathara, Uchitdih, Jarangdih Bottom, Jarangdih, and Jarangdih Top seams, East Bokaro coalfield. The Kathara and Uchitdih seams have also been sampled at two other localities and lateral variation in data in their trace-element and maceral compositions is also evaluated.The East Bokaro coals have: Ba and Sr > 1000 ppm; Mn < 450 ppm; Zr < 400 ppm; Ni and V < 250 ppm; Cr < 185 ppm; La < 165 ppm; Cu, Nb, and B < 125 ppm; Pb, Co and Y < 75 ppm; Ga, Sn, Mo, In and Yb < 15 ppm; Ag 2 ppm; and Ge 7 ppm. Petrographically, the coals are dominant in vitrinite (33–97%), rare in exinite (<15%), and semifusinite (0.8–49%) is the dominant inertinite maceral, with variable mineral and shaly matter (11–30%), graphic representation of trace elements versus vitrinite, inertinite, and coal ash indicates the affinity of (a) vitrinite with Cu, Ni, Co, V, Ga and B; (b) inertinite with Nb and B; and (c) coal ash (mineral matter) with Pb, Cu, Ni, La, Mn and Y; Ba, Cr, Sr, Zr, Cu and Ni are of organic as well as inorganic origins.The trend of the variation patterns and average compositions of the different seams are shown to be distinct and different. The variation along the same profile is inferred to be different for different seams of the coalfield.Trace-element data for certain coals of seams from different coalfields in the Gondwana basins of India are presented. There is a wide difference for each of these basins with respect to certain elements. This is suggestive of the proportions of Cu, Ni, V, Y, Ba, Sr, Cr, B, Zr and Ag, characterizing the different Gondwana Basins. 相似文献
9.
用X-荧光光谱测定岩石中低量稀土元素的仪器参数和测定条件,文[1]已作过讨论。本文介绍样品分析所采用的基本校正,谱线重叠校正和背景处理方法,并将这些方法应用于其他少量和痕量元素的测定。基体的吸收校正岩石样品中最重的主元素是铁,镧系元素La～Er的La线和Ti,Sc,Cr,Mn,Fe, 相似文献
10.
煤矸石是我国堆存量最大的工业固体废物,本文应用电感耦合等离子体发射光谱法、逐级化学提取法和相关性分析研究了淮北临涣矿区低硫煤矸石中10种微量元素的含量及赋存状态,并运用风险评价指数法评价其环境效应。结果表明,低硫煤矸石中Ba、Co、Cr、Mn、Ni、Pb、V含量均高于淮北煤和中国煤均值,Mn、V的富集系数大于1,有一定迁移风险。微量元素主要以残渣态和铁锰氧化物结合态存在,两者质量分数之和为68.87%~92.93%,其中Cd、Co、Cr、Cu、Ni、Pb、Zn赋存于硫化物矿物中,V赋存于黏土矿物中,Mn赋存于碳酸盐矿物和硫化物矿物中。10种微量元素对环境的危害性大小为:MnZnNiPbCdCuBaVCrCo,表明低硫煤矸石堆存过程中活性态Mn对生态环境造成危害的可能性最大,由Mn可能引起的煤矸石山周边地区土壤及水体污染应当重视。 相似文献
11.
The specific chemical and mineral composition of discoid, cake-shaped, and platy ferromanganese nodules (FMNs) from the Chukchi Sea are considered. The main ore components of these FMNs are Fe, Mn, and P. The contents of trace elements (except for Ba and Sr) do not exceed hundredths of percent. Maximum concentrations of most of these elements are specific for the cake-shaped nodules. In general, Mn accumulates most intensely in FMNs. Next (in order of decrease) are Ag(?), Co, and Pb; Sr, Fe, P, Y, and Ca; and Ni, La, Zn, and Cu. As for Ba, Cr, Mg, and K, they do not accumulate in the FMNs. “Dilution” is typical of Si, Al, Na, and Ti. The main ore phases are strengite and amorphous Mn hydroxides. It has been revealed for the first time for the Chukchi Sea that Cu, Zn, Sn, Ni, Pb, W, Bi, Cr, Fe, Ti, Ag, Au, Y, Zr, and La–Nd lanthanides form individual mineral microphases in FMNs: native elements, intermetallic compounds, oxides, and, much more seldom, tungstates, silicates, and phosphates. Accessory ore mineralization is the best pronounced and most diverse in the platy nodules. Though the FMNs from the Chukchi Sea are diagenetic, high-temperature fluids are, most likely, the source of microinclusions of various accessory ore minerals. 相似文献
12.
本文采用四酸溶样ICP6300电感耦合等离子体发射光谱法测试了新疆哈拉奇地区水系沉积物样品中的Li P Ti V Cr Mn Co Ni Cu Zn Sr Y Nb Mo Ba La Pb B W Sn Cd 21种微量元素,明确了该方法测试样品中的Li P Ti V Cr Mn Co Ni Cu Zn Sr Y Nb Mo Ba La 16个元素的检出限、准确度、精密度满足规范（DZ/T0130.2006-2006）要求,而Pb B Cd Sn W5个元素测试质量不能满足规范要求,并对新疆哈拉奇地区水系沉积物采样粒度样品进行了分析测试,验证了该区化探扫面选择10-80目粒度是合适的,但在异常查证工作中要选择10-60目采样粒度更合理。 相似文献
13.
对吉林南部地区煤矿主采煤层中的As、B、Ba、Cd、Cu、Hg、Pb、Se、Sr等微量元素的分析结果表明，太原组与山西组由于成煤环境不同，微量元素组成及含量存在一定的差异：太原组原煤中As、B、Hg、Pb、Se、Zn的含量明显高于山西组，山西组原煤中Ba、Cr、Cu、Mn、V的含量明显高于太原组。吉南煤区原煤中As、B、Hg、Pb、Se明显高于地壳元素平均值，呈富集状态，Co、Cd与地壳平均值接近，其他元素均亏损。与全国煤中微量元素相比，该区原煤中As、Ba、Co、Cr、Cu、Hg、Ni、Pb、Se、V、Zn的含量高于全国平均值，B、Mn、Sr含量低于全国平均值。微量元素赋存状态及相关分析表明，Fe与亲硫有害元素As、Cu、Hg、Pb、Se具有显著相关关系，说明煤中黄铁矿及其他硫化物是许多有害微量元素的重要载体。 相似文献
14.
北山地区植被属戈壁荒漠植被类型，主要植物群落为红沙，红沙中多数元素特别是成矿元素及其伴生元素的含量和变化系数矿区大于背景区，元素含量背景区呈对数正态分布，矿区呈偏对数正态或多峰分布，红沙中的元素组合分类背景区为Au,Cu,Pb,Zn,As,Sb,Mo,V,Mn和Ag,Sn,Sr,Ba及Ti,Cr,Co,Ni,金矿区为Au,Ag,As,Sb,Mo,Mn,Sr和Cu,Pb,Zn,Sn,Ba及Co,Ni,Ti,V,Cr,铜矿区为Cu,Pb,Zn,Mo,Au,Ag,Ba和As,Sb,Sn,Mn及Ti,V,Cr,Co,Ni,Sr，矿区红沙中浓集系数较大的元素多数在矿区岩石中的浓集系统亦较大，金，铜矿床红沙和岩石中的特征元素分别都有Au,Ag,Ag,Sb,Mo,(Mn)和Cu,Pb,(Ba,Ti,Cr)。在金，铜矿床（体上方分别发育有良好的Au和Cu的生物地球化学异常和元素组合及分带，根据红沙的地球化学特征能，判断金或铜矿种类型，并能对掩埋，隐伏金，铜矿床（体）进行定位预测。 相似文献
15.
Delu Li Rongxi Li Zengwu Zhu Xiaoli Wu Futian Liu Bangsheng Zhao Jinghua Cheng Baoping Wang 《中国地球化学学报》2018,37(1):134-150
Using trace elements to reconstruct paleoenvironment is a current hot topic in geochemistry. Through analytical tests of oil yield, ash yield, calorific value, total sulfur, major elements, trace elements, and X-ray diffraction, the quality, mineral content, occurrence mode of elements, and paleoenvironment of the Zhangjiatan oil shale of the Triassic Yanchang Formation in the southern Ordos Basin were studied. The analyses revealed relatively high oil yield (average 6.63%) and medium quality. The mineral content in the oil shale was mainly clay minerals, quartz, feldspar, and pyrite; an illite–smectite mixed layer comprised the major proportion of clay minerals. Compared with marine oil shale in China, the Zhangjiatan oil shale had higher contents of quartz, feldspar, and clay minerals, and lower calcite content. Silica was mainly in quartz and Fe was associated with organic matter, which is different from marine oil shale. The form of calcium varied. Cluster analyses indicated that Fe, Cu, U, V, Zn, As, Cs, Cd, Mo, Ga, Pb, Co, Ni, Cr, Sc, P, and Mn are associated with organic matter while Ca, Na, Sr, Ba, Si, Zr, K, Al, B, Mg, and Ti are mostly terrigenous. Sr/Cu, Ba/Al, V/(V + Ni), U/Th, AU, and δU of oil shale samples suggest the paleoclimate was warm and humid, paleoproductivity of the lake was relatively high during deposition of the shale—which mainly occurred in fresh water—and the paleo-redox condition was dominated by reducing conditions. Fe/Ti ratios of the oil shale samples suggest clear hydrothermal influence in the eastern portion of the study area and less conspicuous hydrothermal influence in the western portion. 相似文献
16.
The Merouane Chott, located in arid southeastern Algeria, experiences annual cycles of filling from September through February
followed by its complete evaporation from February through June. The concentration of 15 trace elements (Li, B, Ti; V, Cr,
Mn, Co, Cu, Ni, Zn, As, Sr, Ba, Pb, Bi, and U) were measured in chott water samples collected from January through June 2003
during the complete evaporation of the lake. The corresponding concentrations of these trace elements in the major external
inputs to this closed basin chott were also obtained. The trace metals show two distinct behaviors. Li, B, Cr, Co, and U tend
to be conserved in the chott waters throughout its evaporation. Much of Cr, Co, and U originated from external sources. It
is likely, therefore, that the concentration of these elements will increase in the chott waters in future years. In contrast,
Ti, Sr, Ba, Zn, Ni, and Pb precipitate continuously during chott evaporation. Of these elements, most of the Sr, Ba, and Zn
originated from outside the chott, and thus it is likely these elements will become increasingly concentrated in the chott
bottom salts with time. V, As, and Cu exhibit intermediate behaviors. These contrasting behaviors are confirmed by analysis
of chott bottom solids. 相似文献
17.
D.A. Spears A.G. Borrego A. Cox R.M. Martinez-Tarazona 《International Journal of Coal Geology》2007,72(3-4):165-176
Laser ablation ICP-MS has been used to produce element profiles from polished coal samples. The elements analysed (V, Ge, Ni, Cu, Zn, Sr and Ba) were those known to have an organic association, with the addition of Al and Fe as controls on the clay and pyrite abundances. The element profiles were compared with the petrography and a statistical analysis was also carried out. Sporinite was found to have low trace element concentrations, inertinite higher concentrations of detrital elements and vitrinite higher concentrations of V, Ge and Al. The relationships between these elements are explored and all are thought to be present in the organic matter and not as minerals. It is thought that these elements became concentrated during diagenesis, with the possibility that some of the Al could be residual. The Cu/Ni ratio in the pyrite is relatively constant, suggesting constant ionic proportions during diagenesis, and possibly a seawater source. 相似文献
18.
The mobilization, redistribution and fractionation of trace elements during chemical weathering processes have been investigated on a 4.05 m thick terra rossa profile overlying dolomite on the Yunnan-Guizhou Plateau, in Southwest China. In this in situ weathering profile, the ferromanganese concretions and the gibbsite spots coexist in the terra rossa saprolite. The mass-balance evaluation reveals that titanium, Nb and Hf in the terra rossa matrix are conservative elements during chemical weathering compared to Zr. The elements of Li, Sc, V, Cr, Fe, Ga, As, Mo, Cs, Ce, Ta, Tl, Pb and Th in the terra rossa matrix include additions from external sources. Beryllium, Mn, Co, Ni, Cu, Rb, Ba and La are depleted in the shallow parts of the terra rossa profile and enriched in the deep parts. The elements of Zn, Sr, Y, Cd, Sn and U in the terra rossa profile are lost during weathering. Compared to the terra rossa matrix, the ferromanganese concretions are significantly enriched in most trace elements, especially Mn, Co, Cd, Ce, Tl and Pb. In contrast, the gibbsite spots are depleted in all trace elements, except for U. The results regarding specific inter-element relationships indicate that most trace elements have different inter-element relationships in the ferromanganese concretions, the gibbsite spots and the terra rossa matrix. This suggests that the behavior of many trace elements during mobilization and redistribution differs from their behavior during incorporation into secondary mineral phases, especially the Mn and Fe oxides and/or oxyhydroxides in the ferromanganese concretions. It is worthy to note that the fractionation between Ce and Mn occurs under intensive chemical weathering conditions. Correspondingly, beryllium exhibits a similar geochemical behavior as that of rare earth elements (except for Ce) and Y during surface weathering. 相似文献
19.
《International Journal of Coal Geology》2005,61(1-2):87-95
The concentration of trace elements and their distribution in the late Permian coal in the Heshan coal field, Guangxi Autonomous Region, were analysed in this paper. The late Permian coal of the Heshan mining district was developed in a low energy and shallow, confined carbonate platform. Heshan coal is a low volatile bituminous coal characterized by a high sulphur content, ranging between 2.0% and 8.2%. Compared with the worldwide average content of the trace elements in coal, the content of some trace element in the study coal is markedly high (Bi, Ce, Cr, Cs, Cu, Ga, Hf, Sr, Ta, Th, U, V, W, Y, Zr, La, Mo, Nb and Sc).The trace element associations were investigated by means of intracorrelation analysis. Some elements, such as Cl, F and Sr are found in coal in association with the carbonate minerals. V, Cr, Zn, Mo, Ni and As contents in coal vary significantly amongst the coal samples. They are mainly concentrated in the lower part of the coal #4 upper of Suhe and Lilan mines and the coal #4 lower of Dong mine, and these possibly occurring in minerals such as arsenide and sulphide. The content of U in Heshan coal is high and is mainly concentrated at the upper and the lower parts of the coal seam and it is associated with mineral assemblages with Ba, Mo, V, Ni, Zn, Rb and Cr. Furthermore, La and Ce are highly correlated with those found in phosphate minerals and Pb, Sc, Ga, Th, Y and Sn to those in aluminosilicate minerals. The enrichment of some elements such as V, Cr, Zn, Mo, Ni, Rb as well as total sulphur and iron in the lower part of most coal seams might be associated with the formation of soil horizon before the accumulation of peat in the basin. Some other elements such as Cl, F, Sr and Ca are locally concentrated in the top of specific coal seams as a result of the leaching from overlying carbonates. 相似文献
20.
Trace element distribution,Co:Ni ratios and genesis of the big cadia iron-copper deposit,new south wales,australia 总被引：9，自引：0，他引：9
Analyses of pyrite, chalcopyrite and magnetite from the volcanic-hosted Big Cadia stratabound iron-copper deposit in Central Western New South Wales show considerable variation in the minor elements Mn, Ba, Ag, Pb, Zn, Cd, Se, Co and Ni. The preferential concentration of Co and Cd in pyrite, Zn and Ag in chalcopyrite and Mn in magnetite can be attributed to variations in activities of the ions in the hydrothermal fluid at the time of crystallisation of the mineral phases, or in cases such as the concentration of Co in pyrite, dependent on compatible electronic spin states between Co2+ and Fe2+. Trace element concentrations, especially Co and Ni contents and Co:Ni ratios in pyrite (average Co:Ni ratio=17.1) support a volcanic exhalative origin of mineralisation at Big Cadia. Differences in trace element composition such as higher Ni contents in pyrite in contrast with other volcanic-hosted ores may reflect the more basic character of volcanic rocks underlying the Big Cadia deposit. 相似文献