王台山地区韧性剪切带型金矿成因

五台山地区韧性剪切带型金矿分布地晚太古代碰撞造山带中，与世界许多太古宙绿岩带型金矿具有相似的特征。研究表明：成矿流体的δ＾１８ＯＨ２Ｏ＝－２．１‰－４．９‰，δＤ＝－６９－１１２‰，蚀谜面对得起盐矿物的δ＾１３ＣＰＤＢ＝－２．０－１．４‰，δ＾１８ＯＳＭＯＷ－１０．０－２０．０‰，载金黄铁矿的δ＾１４Ｓ＝－３．７－５．６‰。成矿前流体具有一高盐度，成矿期流体以富含ＣＯ２、近似海水的δ＾１８Ｏ和海相     

扬子板块东南大陆边缘上震旦统热水成因硅质岩的地球化学标志

晚震旦世时,在扬子板块东南大陆边缘地带发育一套层状硅质岩建造,岩石化学成分纯净,ＳｉＯ２含量在９０％以上,其它化学成分含量均很低。但Ｆｅ和Ｍｎ相对富集,而Ａｌ,Ｔｉ,Ｍｇ相对贫乏。微量元素含量变化大,大部分微量元素含量相对地壳克拉克值偏低,仅Ｕ,Ａｓ,Ｓｂ,Ａｇ,Ｂａ等富集。岩石的δ＾３０Ｓｉ为０．０‰～０．７‰,δ＾１８Ｏ为２０．２‰～２３．６‰,δ＾３０Ｓｉ和δ＾１８Ｏ值及岩石的形成温度清楚地     

东天山康古尔金矿床成矿流体地球化学特征及其来源

新疆康古尔金矿床是分布于晚古生代火山岩区受脆韧性剪切带控制的蚀变岩型金矿。该矿床成矿流体具有中低温度（３２０～１００℃）、中等ＮａＣｌ质量分数（１１４％～１７０％）、弱还原等特征。包裹体气相成分以Ｈ２Ｏ和ＣＯ２为主,液相成分中富Ｎａ＋、Ｃｌ－,而贫Ｋ＋、Ｆ－。成矿流体δＤ为－４５‰～－６６‰,δ１８Ｏ为－８３４‰～２９８‰,（８７Ｓｒ／８６Ｓｒ）ｉ值为０７０７７～０７１０６,反映了成矿流体由变质水、大气降水和岩浆水混合组成的特点     

等离子体发射光谱法测定重晶石中钡铁和硅

重晶石经Ｎａ２ＣＯ３熔融,水浸取,过滤。沉淀经ＨＣｌ溶解后,用电感耦合等离子体发射光谱法同时测定主成分ＢａＳＯ４和次量成分Ｆｅ２Ｏ３以及滤液中的ＳｉＯ２,结果与部颁标准方法符合。方法精密度好,主量组分ＢａＳＯ４测定的ＲＳＤ（ｎ＝６）为０．２４％,次量组分Ｆｅ２Ｏ３和ＳｉＯ２的ＲＳＤ（ｎ＝６）分别是３．６９％和１．４５％。     

矿物3CaO·3Al_2O_3·BaSO_4形成过程研究

ｅｏｒｅａｎｕ等［１］研究ＣａＯＡｌ２Ｏ３Ｍｘ（ＳＯ４）Ｙ［Ｍ＝Ｍｇ２＋、Ｓｒ２＋、Ｂａ２＋、Ｚｎ２＋、Ｆｅ２＋、Ｆｅ３＋、Ａｌ３］系统中,形成类似于矿物３ＣａＯ·３Ａｌ２Ｏ３·ＣａＳＯ４（硫铝酸钙）的可能性时,报道合成了新矿物３ＣａＯ·３Ａｌ２Ｏ３·ＢａＳＯ４（简写为３ＣＡ·ＢａＳＯ４）;部分学者［２,３］研究过它的胶凝性能等。在有关文献中,研究者制备研究用纯矿物的煅烧条件、获得样品的矿相组成不尽相同。如文献［１］在温度１４００℃保温２４０ｍｉｎ,制备的样品包括铝酸钙（ＣａＯ·Ａｌ２Ｏ３…     

催化还原褪色光度法测定痕量锡

痕量锡在０．０４ｍｏｌ／ＬＨ３ＰＯ４介质中对ＮａＨ２ＰＯ２还原罗丹明Ｂ褪色反应有催化作用,催化程度与Ｓｎ量、温度和加热时间线性相关。基于此,建立了痕量锡的动力学光度分析方法。方法检出限为０．０３４μｇ／Ｌ,线性范围为０～２０μｇ／Ｌ,结合磷酸三丁酯色谱分离,实现了地质样品中痕量Ｓｎ的测定。方法经国家地质标准物质分析验证,结果与标准值相符。对于ｗ（Ｓｎ）为１０－６水平的试样其ＲＳＤ（ｎ＝６）＜６．５％。     

二溴羟基苯基荧光酮与铁显色反应及应用

在溴化十六烷基三甲铵（ＣＴＭＡＢ）存在下，ｐＨ为７０～７４的Ｎａ２Ｂ４Ｏ７ＫＨ２ＰＯ４缓冲溶液体系中，铁与二溴羟基苯基荧光酮（ＤＢＨ＿ＰＦ）形成１∶３的络合物，其最大吸收波长为６００ｎｍ，表观摩尔吸光系数为１１５×１０５Ｌ·ｍｏｌ－１·ｃｍ－１，铁质量浓度在０～０３２ｍｇ／Ｌ符合比尔定律。该方法经硅质砂岩、石灰岩、石膏标样分析验证，结果与标准值相符，ＲＳＤ（ｎ＝５）小于３１％。     

特种含钛合成材料中主成分的测定

特种含钛合成材料中主成分的测定郎庆勇北京地矿部岩矿测试技术研究所１０００３７采用Ｋ＿２Ｓ＿２Ｏ＿７熔融分解特种含钛合成材料ＢａＴｉＯ＿３和ＳｒＴｉＯ＿３，稀Ｈ＿２ＳＯ＿４浸取。沉淀的ＢａＳＯ＿４和ＳｒＳＯ＿４用于重量法测ＢａＯ和ｓｒＯ；滤液用于Ｈ＿２...     

五台山地区韧性剪切带型金矿成因

五台山地区韧性剪切带型金矿分布于晚太古代碰撞造山带中，与世界许多太古宙绿岩带型金矿具有相似的特征。研究表明：成矿流体的δ１８ＯＨ２Ｏ＝－２．１‰～４．９‰，δＤ＝－６９‰～－１１２‰，蚀变碳酸盐矿物的δ１３ＣＰＤＢ＝－２．０‰～－１．４‰，δ１８ＯＳＭＯＷ＝１０．０‰～２０．０‰；载金黄铁矿的δ３４Ｓ＝－３．７‰～５．６‰。成矿前流体具有中—高盐度，成矿期流体以富含ＣＯ２、近似海水的δ１８Ｏ和海相碳酸盐的δ１３Ｃ值，成矿后流体具有较高的盐度及可变的δ１８ＯＨ２Ｏ、δ１３Ｃ值。这种金矿成矿流体很难与某单一流体源相对应，它反映的多是变质流体与海盆地铁镁质岩石在成岩过程中饱含的热卤水混合的结果。综合有关资料，提出本区韧性剪切带型金矿形成于太古宙末期汇聚型地球动力学背景下的弧－陆、陆－陆碰撞过程中，金矿化作用和分布受碰撞构造边界的大规模逆冲型韧性剪切带控制。     

复杂地质样品中铀,钍等成分X射线荧光光谱分析

本文提出了一种用ＸＲＦ测定复杂地质样品全分析中其它特殊成分的分析方法。本方法采用熔融法制备样片，个别元素采用压片法制样，用散射内标法与经验α系数相结合的方法进行基体效应的校正。各氧化物的测定下限分别为：ＳｒＯ０．００３０％，ＺｒＯ２０．００３０％，ＰｂＯ０．００３６％，ＣｕＯ０．００４２％，ＮｉＯ０．００２７％，ＺｎＯ０．００２１％，Ｃｒ２Ｏ３０．００６９％，ＢａＯ０．００４８Ｋ，Ａｓ２Ｏ３０．００１５％，Ｎｂ２Ｏ５０．００４８％，Ｖ２Ｏ５０．００５１％，ＴｈＯ２０．００３６％，Ｕ３Ｏ８０．００３０％，其分析结果的精密度和准确度较好，能够满足地质研究工作的需要。     

中高含硫量煤中硫的形态分析

利用超声提取、高速离心分离和加入助分散剂等手段，实现了中，高含硫量煤中单质硫，硫酸盐硫，硫化物硫，有机硫等主要形态硫的分步提取和顺序测定。所建分析方法测定了国家一级标样，统样样品和部分有分析结果的样品，其主要形态硫的加和与标准样品参考值，统检样品定值，原样品的总硫分析结果相符，RSD（n=3)为0．80％－4．23％，方法可用于煤中各主要形态硫的测定。     

红外碳硫仪测定矿石中高含量硫的探讨

探讨了用红外碳硫测定仪测定矿石中高含量硫需注意的一些影响因素,包括标样的选择、减少天平误差、称样量、样品的充分燃烧以及仪器的稳定性,说明了用红外碳硫仪测定矿石中高含量硫的可行性。     

Quantitative Recovery of Elemental Sulfur and Improved Selectivity in a Chromium-Reducible Sulfur Distillation

Chromium-reducible sulfur (CRS) distillations are intended to recover only reduced inorganic sulfur compounds (RIS) including elemental sulfur. However, the quantitative recovery of elemental sulfur is not ensured in common CRS-distillations. The new method presented here was designed to remedy this deficiency. An increase in ethanol concentration assured the quantitative recovery of elemental sulfur in various forms and, in addition, all other RIS-compounds were quantitatively recovered. Furthermore, the selectivity of the procedure was improved by an additional filtration step to eliminate zinc particles from the Cr(II)-solution. Thus, the recovery of sulfates and organic sulfur compounds was significantly decreased by a factor of up to 35, depending on the compound analysed. Exhaustive testing with a variety of pure phases, rock and soil samples demonstrated the precision and accuracy of the new method. The new protocol eliminated the constraints of previous procedures. The improved distillation efficiency for elemental sulfur ensured the quantitative recovery of all RIS-compounds in a single-step distillation.     

电感耦合等离子体质谱法测定硫时不同形态硫的影响

电感耦合等离子体质谱(ICP-MS)常常被应用于矿石、蛋白质和化石燃料等材料中硫含量的测定。文章综合研究比较了四极杆电感耦合等离子体质谱(Q-ICP-MS)和扇形磁场电感耦合等离子体质谱(SF-ICP-MS)测定硫的灵敏度、检出限及空白干扰。重点考察了两种不同的样品介质(水和2% HNO₃)中不同形态的硫对SF-ICP-MS测定硫信号的影响,并且深入研究了影响的原因。结果表明,硫含量相同但形态不同的含硫阴离子(S^2-、S₂O₃^2-、SO₃^2-、SO₄^2-)在2%的HNO₃介质中的信号比在水介质中的信号稳定,2%的HNO₃更适合于作为ICP-MS测定硫的介质。在2%的HNO₃介质中,S^2-、SO₃^2-中S的ICP-MS测量灵敏度(即标准曲线的斜率)分别为7828 cps/(μg·L^-1)、5528 cps/(μg·L^-1),SO₄^2-和S₂O₃^2-的测量灵敏度分别是为1321 cps/(μg·L^-1)、1299 cps/(μg·L^-1)。S^2-和SO₃^2-的灵敏度分别约为SO₄^2-的6倍和4倍;而S₂O₃^2-的灵敏度与SO₄^2-基本一致。主要原因在于S^2-、SO₃^2-形态的硫在HNO₃介质中形成了气态的H₂S和SO₂,相当于提高了雾化效率,从而使这两种形态硫的灵敏度大幅度提高。     

Sulfur mobility in peat

Lead-210 chronologies, vertical S concentration gradients and δ³⁴S values are presented for 5 Sphagnum-dominated peat bogs located in Central Europe (Rybarenska slat and Ocean Bog; Czech Republic) and the British Isles (Thorne Moors, England; Connemara, Ireland; and Mull, Scotland). Sulfur concentrations were measured in three 40-cm deep peat cores per site, sectioned into 2-cm segments. The coefficient of variation in S concentrations was low across all depths and sites (mean of 16%), indicating a high degree of within-site homogeneity in vertical S patterns. Similar S concentration trends and similar δ³⁴S trends were found at all study sites. With an increasing peat depth, S concentrations first increased and then decreased. S concentrations peaked in layers which were deposited in ca. 1959, 1907, 1945, 1899 and 1799 at Rybarenska slat, Ocean, Thorne Moors, Connemara and Mull, respectively. Atmospheric S deposition peaked in 1972 in the UK and in 1987 in the Czech Republic. Due to downward S mobility in peat, S concentration maxima were found in layers 59 (±19) a older that the year of the actual peak in S input. With an increasing depth, the maturating peat substrate at all sites exhibited first a negative δ³⁴S shift, resulting from dissimilatory bacterial SO₄ reduction, and then a positive δ³⁴S shift, which may be related to advancing S mineralization. Minimum δ³⁴S values were detected in layers which were deposited in ca. 1988, 1982, 1945, 1940 and 1978. A comparison of historical δ³⁴S signatures of atmospheric S in England, measured on archived grain from the Broadbalk experiment (1845–1994), with δ³⁴S values of Thorne Moors peat (1830–1994) also indicated mobility of S in peat. Sulfur mobility in water-logged peat is of concern during the present period of easing industrial pollution because SO₄ released from peatlands may increase the acidity of the output.     

蒋家坪矿区高硫煤中有机硫的特性研究

运用煤岩学、煤化学、地球化学等学科的理论与方法,对湖南蒋家坪矿区煤质、煤岩特征和形态硫进行分析,结果显示：所测样品全硫含量为8％～10．1％,其中有机硫含量高达6％,属高有机硫煤;煤样的显微组分以镜质组为主,含量接近80％,惰质组中以丝质体、半丝质体和碎屑惰质体为主,矿物则多以黄铁矿和黏土矿物为主。通过对煤中成煤植物类型、凝胶化程度、镜惰比和氧化指数的研究,认为矿区高硫煤形成于比较潮湿的弱氧化条件下。     

Sulfur Variations in Glasses from Volcanic Rocks: Effect of Melt Composition on Sulfur Solubility

A worldwide data set of major element and sulfur analyses of undegassed lavas, pumices, and melt inclusions from 14 volcanic locations was selected to investigate the compositional effects on sulfur solubility in magmas. We utilized analyses on calc-alkaline, alkaline, and tholeiitic rocks, with a range of 3400 ppm S variation. There is a strong correlation between chemical composition and the sulfur concentration: the less silicic and the more alkaline the rocks are, the more dissolved sulfur they can carry. Also, sulfur concentration is higher in rocks that represent less polymerized melts. Elemental correlations between FeO and S, well-defined for tholeiites, do not hold for alkaline melts. The compositional effects are at least as important as the better-known pressure, temperature, and f(O₂) dependencies.     

Stable Sulfur Isotopic Evidence for Historical Changes of Sulfur Cycling in Estuarine Sediments from Northern Florida

Data on abundance and isotopic composition of porewater and sedimentary sulfur species are reported for relatively uncontaminated and highly contaminated fine-grained anoxic sediments of St. Andrew Bay, Florida. A strong contrast in amount and composition of sedimentary organic matter at the two sites allows a comparative study of the historical effects of increased organic loading on sulfur cycling and sulfur isotopic fractionation. In the contaminated sediments, an increase in organic loading caused increased sedimentary carbon/sulfur ratios and resulted in higher rates of bacterial sulfate reduction, but a lower efficiency of sulfide oxidation. These differences are well reflected in the isotopic composition of dissolved sulfate, sulfide, and sedimentary pyrite. Concentration and isotopic profiles of dissolved sulfate, organic carbon, and total sulfur suggest that the anaerobic decomposition of organic matter is most active in the upper 8cm but proceeds at very slow rates below this depth. The rapid formation of more than 90% of pyrite in the uppermost 2 cm which corresponds to about 3 years of sediment deposition allows the use of pyrite isotopic composition for tracing changing diagenetic conditions. Sediment profiles of the sulfur isotopic composition of pyrite reflect present-day higher rates of bacterial sulfate reduction and lower rates of sulfide oxidation, and record a profound change in the diagenetic cycling of sulfur in the contaminated sediments coincident with urban and industrial development of the St. Andrew Bay area.     

Sulfur isotope ratios of Icelandic rocks

Sulfur isotope ratios have been determined in 27 selected volcanic rocks from Iceland together with their whole rock chemistry. The ³⁴S of analyzed basalts ranges from –2.0 to +0.4 with an average value of –0.8 Tholeiitic and alkaline rocks exhibit little difference in ³⁴S values but the intermediate and acid rocks analyzed have higher ³⁴S values up to +4.2 It is suggested that the overall variation in sulfur isotope composition of the basalts is caused by degassing. The small range of the ³⁴S values and its similarity to other oceanic and continental basalts, suggest that the depleted mantle is homogeneous in its sulfur isotope composition. The ³⁴S of the depleted mantle is estimated to be within the range for undegassed oceanic basalts, –0.5 to +1.0     

莱芜潘西煤矿降低高硫煤含硫量的几点措施

根据目前国内煤炭脱硫技术的发展现状,该文分析研究了潘西煤矿的煤质特征和硫的赋存状态特征。为了降低商品煤中的硫分,潘西煤矿采取了筛选和捡选原煤中黄铁矿结核降低商品煤硫分,上下组煤合理配采降低商品煤硫分,洗选法降低硫分等措施,使煤的质量明显提高,获得了较好的经济效益。