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1.
小秦岭文峪金矿床流体包裹体研究及矿床成因   总被引：5，自引：2，他引：3  
周振菊  蒋少涌  秦艳  赵海香  胡春杰 《岩石学报》2011,27(12):3787-3799
文峪金矿位于小秦岭矿田南部,其产出受脆-韧性剪切带控制,赋矿围岩为太华群变质杂岩.根据脉体穿切关系和矿物交代关系,可以将文峪金矿流体成矿过程分为早、中、晚三个阶段,其热液石英中发育CO2-H2O型、纯CO2型和H2O溶液型三种类型流体包裹体.平阶段石英中原生包裹体主要是CO2-H2O型和纯CO2型,其成分为CO2+H2O±N2±CH4,均一温度集中在290～330℃,盐度为1.02％～9.59％ NaCleqv;中阶段为主成矿阶段,该阶段石英中包含了所有3种类型的包裹体,其中以CO2-H2O型包裹体为主,获得CO2-H2O和水溶液包裹体均一温度集中在250～290℃,盐度为0.02％～12.81％NaCleqv;晚阶段石英仅发育水溶液型包裹体,具有较低的均一温度(114～239℃)和盐度(4.18％～8.95％ NaCleqv).根据CO2-H2O型包裹体计算早、中阶段压力分别为130 ～ 178MPa和85 ～ 150MPa,对应的成矿深度分别为4.7～6.5km和3.1～5.5km.总体而言,文峪金矿的初始流体具有中高温、富CO2、低盐度的变质流体特征,晚成矿阶段流体演化为低温、低盐度水溶液流体,流体的不混溶导致了主成矿期矿质的大量沉淀,文峪金矿为中浅成的造山型矿床.  相似文献   

2.
新疆东天山白山钼矿床流体包裹体研究   总被引：5，自引：3，他引：2  
白山钼矿位于东天山觉罗塔格成矿带东段,是新疆极具代表性的大型-超大型斑岩钼矿.根据矿物共生组合和脉体穿插关系,脉体发育顺序依次为:早期石英-钾长石脉、石英-钾长石-辉钼矿脉、石英-辉钼矿脉、石英-多金属硫化物脉和晚期石英-碳酸盐-萤石脉.早期石英-钾长石脉中主要发育纯CH4包裹体(PC型)、CH4-H2O型包裹体(C1型)和水溶液包裹体(W型),均一温度集中在320 ～420℃,盐度为1.98％ ～ 8.79％ NaCleqv;石英-钾长石-辉钼矿脉中发育含子晶包裹体(S型)和W型包裹体,均一温度集中在260～ 400℃,盐度为1.49％～8.65％ NaCleqv;石英-辉钼矿脉和石英-多金属硫化物脉发育W型、S型和CO2-H2O型包裹体(C2型),均一温度分别为200～ 240℃和140 ～ 240℃,盐度分别为2.14％ ～8.10％ NaCleqv和0.33％～ 10.22％ NaCleqv,不包括不熔子矿物的贡献;晚期石英-碳酸盐-萤石脉只发育W型包裹体,均一温度和盐度明显下降,分别为100～ 160℃和0.17％～4.86％ NaCleqv.估算的石英-钾长石脉体和石英-多金属硫化物脉形成压力分别为105 ～ 221 MPa和15 ～ 285MPa.成矿流体由高温、富碳质、还原的岩浆流体向低温、低盐度、贫碳质的大气降水热液演化.成矿阶段温度下降,早期流体中的CH4还原HMoO4-的高价钼,从而形成辉钼矿,可能是导致成矿物质沉淀的重要因素.  相似文献   

3.
河南省栾川南泥湖斑岩型钼钨矿床流体包裹体研究   总被引：20，自引：11，他引：9  
杨永飞  李诺  杨艳 《岩石学报》2009,25(10):2550-2562
河南省栾川县南泥湖超大型钼钨矿床形成于秦岭造山带的燕山期大陆碰撞体制,流体成矿过程包括早、中、晚3个阶段,分别以石英+钾长石±辉钼矿±黄铁矿、石英+多金属硫化物±碳酸盐和石英+碳酸盐+萤石组合为标志,矿石矿物主要沉淀于中阶段.早、中阶段石英中可见纯CO_2包裹体、CO_2-H_2O型包裹体、水溶液包裹体和含子晶多相包裹体,但晚阶段萤石中只发育水溶液包裹体.早阶段流体包裹体均一温度集中于350～460℃,盐度为5.68 wt%～17.87 wt% NaCl.eqv.中阶段包裹体均一温度集中在250～380℃,盐度为3.00 wt%～38.16 wt% NaCl.eqv;中阶段多相包裹体中常见石盐、黄铜矿和未知种类的子矿物,指示流体具有沸腾所致的还原性、过饱和特征;盐度相差悬殊的含子晶多相包裹体、富气相水溶液包裹体和富液相水溶液包裹体共存,在相近温度下异相均一,表明流体沸腾的存在.晚阶段流体包裹体均一温度集中在115～265℃,盐度介于0.53 wt%～1.23 wt%NaCl.eqv之间.估算早、中阶段流体捕获压力分别为70～300MPa和30～150MPa,推测成矿深度约为3km.总之,成矿流体具高温、高盐度、高氧逸度、富CO_2的特征;流体沸腾导致CO_2逃逸,氧化性降低,成矿物质沉淀.  相似文献   

4.
新疆阿尔泰塔拉特铁铅锌矿床流体包裹体研究及矿床成因   总被引：4，自引：1，他引：3  
李登峰  张莉  郑义 《岩石学报》2013,29(1):178-190
塔拉特铁铅锌矿位于新疆阿尔泰造山带南缘的阿巴宫多金属成矿带,矿体赋存于克兰盆地下泥盆统康布铁堡组中,为一套海相中酸性火山岩-火山碎屑岩、陆源碎屑沉积岩-碳酸盐岩建造,脉状矿体受阿巴宫大断裂次级断裂控制.根据矿物组合和脉体穿插关系,塔拉特铁铅锌矿可分为4个成矿阶段:矽卡岩,氧化物,硫化物和碳酸盐阶段,后3个阶段均有石英共生.其中,硫化物(方铅矿-闪锌矿±磁黄铁矿±黄铜矿)阶段是铅锌成矿的主要阶段.不同阶段石英中广泛发育流体包裹体,可分为水溶液包裹体(W型)、纯CO2包裹体(PC型)、CO2-NaCl-H2O包裹体(C型)及含子矿物多相包裹体(S型)4类.冷热台显微测温和激光拉曼分析表明,氧化物阶段石英含有4种类型的包裹体,以W型为主,C型和S型包裹体次之,包裹体均一温度介于271～ 426℃,W型和C型盐度范围0.5％～22.4％ NaCleqv,S型包裹体盐度30.5％ ～40.6％ NaCleqv;硫化物阶段的石英流体包裹体为W型、C型和PC型,均一温度为204 ～ 269℃,盐度介于0.2％～15.6％ NaCleqv之间;碳酸盐阶段的矿物只含W型包裹体,均一温度集中在175～211℃之间,盐度为1.1％ ～9.9％ NaCleqv.利用C型包裹体对硫化物阶段成矿压力估算,得到107 ～ 171MPa,对应深度为4～6km.塔拉特铁铅锌矿初始成矿流体具有高温、高盐度、富CO2的特征,但碳酸盐阶段低盐度、贫CO2,流体不混溶和混合作用导致了成矿物质的沉淀.塔拉特铁铅锌矿的地质和成矿流体特征显示其为碰撞造山体制形成的矽卡岩型成矿系统.  相似文献   

5.
河南王坪西沟铅锌矿床流体包裹体特征和矿床成因类型   总被引：9，自引：6，他引：3  
王坪西沟铅锌矿床隶属于东秦岭外方山钼铅锌多金属成矿区,位于车村-鲁山断裂北侧。矿床赋存于中元古代熊耳群鸡蛋坪组火山岩系中,受断裂控制,呈脉状产出;矿石主要由金属硫化物,少量石英和碳酸盐组成;成矿过程分为早、中、晚三个阶段,分别以石英-黄铁矿组合、金属硫化物和碳酸盐为标志。流体包裹体研究表明,成矿流体为CO2-H2O-NaCl±CaCl,体系,石英或闪锌矿中可见CO2-H2O型、含子晶型和水溶液型三类包裹体,CO2-H2O型包裹体集中在早阶段产出。早、中、晚阶段流体包裹体均一温度分别为280～386℃、180～350℃和120-230℃,从早到晚逐渐降低;盐度分别集中在3％～7％NaCl eqv．、3．55％～17．43％NaCl eqv．和3．06％-13．51％NaCleqv．。含子晶型流体包裹体主要出现在中阶段,子晶为方解石,该阶段为成矿主要阶段,可见CO2-H2O型包裹体与富液相水溶液包裹体共存,均一温度相近,指示流体沸腾,发生CO2的逃逸,成矿物质快速沉淀。总之,王坪西沟铅锌矿床地质特征与造山型矿床一致,成矿机理可由碰撞成岩成矿与流体作用（CMF）模式所解释。  相似文献   

6.
内蒙古车户沟钼铜矿成矿年代学及成矿流体特征研究   总被引：2，自引：1，他引：1  
孟树  闫聪  赖勇  舒启海  孙艺 《岩石学报》2013,29(1):255-269
内蒙古车户沟斑岩钼铜矿床位于西拉木伦钼矿带内.含矿花岗斑岩的LA-ICP-MS锆石U-Pb年龄为251.6±3.2Ma,9件辉钼矿样品Re-Os同位素等时线年龄为250.2±7.2Ma,表明成矿作用发生在早三叠世.车户沟钼铜矿床成矿流体演化可分为矿前阶段、早阶段、中阶段和晚阶段.矿前阶段以斑晶石英+磁铁矿为标志,流体以高温、低盐度、富CO2为特征;早阶段是辉钼矿沉淀的主要阶段,流体包裹体均一温度分布范围为210 ～ 423℃,盐度范围为5.3％ ～45.8％ NaCleqv,部分不同类型不同盐度的包裹体密切共生,但均一温度接近,指示沸腾作用发生;中阶段为黄铜矿沉淀的主要阶段,未见含CO2包裹体,流体包裹体均一温度为210 ～ 391℃,盐度范围为1.7％ ～43.8％ NaCleqv;晚阶段为石英-碳酸盐±黄铁矿脉,只发育富液相水溶液包裹体,均一温度低于260℃,盐度为2.4％～11.4％ NaCleqv.因此,车户沟矿床成矿流体由初始的高温、富CO2,经沸腾作用和CO2逃逸,演化为低温、贫CO2.车户沟氢氧同位素特征早阶段流体(δ18OH2o=5.1‰～5.7‰,δDH2o=-91‰ ～-88‰)属于岩浆热液,中、晚阶段(δ18OH2O=-5.1‰～4.2‰,δDH2O=-105‰～-84‰)介于岩浆水和大气降水之间,指示成矿过程中有大气降水加入.  相似文献   

7.
矿床石英脉中发育3种类型的流体包裹体:C型、PC型及W型包裹体.测温结果显示:早阶段C型包裹体均一温度为340℃～480℃,盐度为6.1％～9.1％NaCleqv;中阶段3种类型的包裹体均发育,均一温度为220℃～460℃,盐度5％～15.2％NaCleqv;晚阶段只发育"W"型包裹体,均一温度为140℃～300℃,盐...  相似文献   

8.
道伦达坝矿床位于大兴安岭南段,是一个中型的铜钨锡银矿床。矿体主要产于二叠系砂板岩中的断裂破碎带中,华力西期黑云母花岗岩中的断裂破碎带中亦赋存有矿体。该矿床的成矿过程可划分为4个阶段：石英萤石白云母电气石锡石黑钨矿阶段(Ⅰ阶段)、石英萤石黑钨矿黄铜矿毒砂磁黄铁矿阶段(Ⅱ阶段)、石英萤石黄铜矿黄铁矿磁黄铁矿银矿物阶段(Ⅲ阶段)和方解石萤石黄铁矿阶段(Ⅳ阶段)。道伦达坝矿床主要发育富液两相包裹体(WL型)、富气两相包裹体(WG型)和含子矿物多相包裹体(S型)。Ⅰ和Ⅱ阶段均发育WL型、WG型和S型包裹体,两阶段的均一温度和盐度分别介于309～389 ℃和242～339 ℃、6.2%～46.3% NaCleqv.和5.3%～41.4% NaCleqv.;Ⅲ阶段主要发育WL型和S型包裹体,均一温度介于153～268 ℃,盐度介于3.5%～35.4% NaCleqv.;Ⅳ阶段仅发育WL型包裹体,均一温度介于114～188 ℃,盐度介于2.1%～7.6% NaCleqv.。前两个阶段为中高温、高盐度流体,Ⅲ阶段流体具中低温、高盐度特征,而Ⅳ阶段为低温、低盐度流体。矿床的δ18OH2O值介于-10.0‰～7.2‰,δD值介于-127‰～-81‰,由Ⅰ阶段到Ⅳ阶段,成矿流体由以岩浆流体为主逐渐演化到以大气降水为主,表明道伦达坝矿床初始流体为岩浆热液,后期有大气降水的加入。硫同位素组成(-7.4‰～-1.2‰)表明成矿物质主要来自深源岩浆;铅同位素组成(μ值介于9.3～9.7)暗示成矿物质主要来自造山带物质部分熔融形成的岩浆。流体的多次沸腾和混合是矿质沉淀的主要机制。  相似文献   

9.
岔路口超大型斑岩钼矿床位于大兴安岭北部,是目前中国东北地区最大的钼矿床,矿体赋存于中酸性杂岩体及侏罗系火山-沉积岩内,其中花岗斑岩、石英斑岩、细粒花岗岩与钼矿化关系密切.流体包裹体研究表明,岔路口矿床主要发育富液两相包裹体、富气两相包裹体和含子矿物多相包裹体.花岗斑岩石英斑晶中流体包裹体的形成温度集中在230 ～ 440℃和470～510℃两个温度区间,盐度分别介于0.7％ ～ 53.7％ NaCl eqv和6.2％～61.3％ NaCl eqv两个区间;成矿早阶段钾长石-石英-磁铁矿脉中流体包裹体的形成温度集中在320～440℃、盐度介于4.2％ ～ 52.3％NaCl eqv;成矿中阶段石英-辉钼矿脉和角砾岩中流体包裹体的形成温度集中在260～410℃、盐度介于0.4％～52.3％ NaCleqv;成矿晚阶段石英-萤石-方铅矿-闪锌矿脉中流体包裹体的形成温度集中在170～320℃、盐度介于0.5％ ～ 11.1％ NaCleqv.成矿流体具高温、高盐度及高氧逸度的特征,总体上属于富F的H2O-NaCl±CO2体系.成矿流体的δ 18Ow值为-4.5‰～3.2‰,δDw值为-138‰～-122‰,表明成矿流体为岩浆水与雨水的混合流体.金属硫化物的δ34S值介于-1.9‰～+3.6‰,均值为+1.6‰,表明成矿物质主要来自深源岩浆.多期次的流体沸腾作用是该矿床的主要成矿机制.  相似文献   

10.
新疆萨热阔布金矿床流体包裹体研究及矿床成因   总被引：2，自引：0，他引：2  
新疆萨热阔布金矿床位于阿尔泰造山带南缘克兰火山-沉积盆地内,矿体呈脉状产于康布铁堡组上亚组地层中(D1k2)。不同成矿阶段石英脉中广泛发育流体包裹体,可划分为H2O-CO2包裹体(C型)、纯CO2包裹体(PC型)、水溶液包裹体(W型)及含子矿物多相包裹体(S型)四类。测温结果显示,成矿早阶段主要发育C型和PC型包裹体,均一温度范围为271～446℃,流体盐度介于5.9%～8.4%NaCleqv之间;中阶段主要发育C、PC、W和S型包裹体,均一温度低于早阶段,为236～374℃,流体盐度介于4.8%～15.0%NaCleqv之间;晚阶段主要发育W型包裹体,均一温度范围为139～264℃,流体盐度介于1.1%～6.9%NaCleqv之间。对成矿压力和深度的估算表明,成矿压力为90～330MPa,成矿深度为9～12km。综上所述,萨热阔布金矿成矿流体具有富CO2、中低盐度的变质流体特征,流体沸腾导致了成矿物质的沉淀。结合矿床地质特征,萨热阔布金矿床属于造山型金矿床。  相似文献   

11.
The photoluminescence (PL) spectra, excitation spectra, and PL decay curves of natural, heat-treated, and γ-ray-irradiated thenardites from Ai-Ding Salt Lake, Xinjiang, China, were studied. The natural thenardite under 300 nm excitation showed milk-white luminescence, and the PL spectrum consisted of an extremely broad band with a peak located at approximately 509 nm, spreading over a wide range of UV and visible wavelengths. The excitation spectra, obtained by monitoring the luminescence at 530 nm, consisted of a broad band with a peak located at approximately 235 nm and a flat band spreading over a wide range of UV and visible wavelengths. The PL decay curve of natural thenardite consisted of a fast-decay component with a lifetime of less than 0.1 μs and a slow-decay component with a half-decay time of approximately 0.4 s. The heat treatment of thenardite at 900°C for 20 min reduced the luminescence efficiency to 1/100. The γ-ray irradiation of thenardite reduced the luminescence efficiency to approximately half.  相似文献   

12.
钒钛磁铁矿样品经过氧化钠熔融,盐酸提取,溶液分取稀释后用电感耦合等离子体发射光谱法同时测定其中的V2O5、TiO2、Co、Ni。实验确定过氧化钠的用量为1.5 g,盐酸的用量为10 mL,选择干扰元素较少和背景干扰较小的V、Ti、Co、Ni分析谱线分别为292.4 nm、334.9 nm、230.7 nm、231.6 nm,在稀释因子为10(总稀释因子5000)的条件下进行分析,方法检出限为0.05～0.17μg/g。用国家一级钒钛磁铁矿标准物质GBW 07225(原矿)、钒钛磁铁矿标准物质GBW 07226a(精矿)、钒钛磁铁矿标准物质GBW 07227(尾矿)验证方法精密度和准确度,方法精密度(RSD,n=12)为0.41%～1.91%;除含量较低的Ni和Co外,相对误差(RE,n=4)均小于5%。通过安装氩气加湿器有效地解决了盐分较大带来的影响,在标准系列中加入等量空白溶液,保持基体与试样一致,消除了基体效应。方法分解样品彻底完全,分析流程简单,易于掌握,一次熔样可以同时测定多种元素,可适用于大批量样品分析。  相似文献   

13.
Torsion experiments were performed on the Al2SiO5 polymorphs in the sillimanite stability field to determine basic rheological characteristics and the effect of deformation on polymorphic transformation. The experiments resulted in extensive transformation of andalusite and kyanite to sillimanite. No transformation occurred during the hot-press (no deformation) stage of sample preparation, which was carried out at similar P–T conditions and duration as the torsion experiments. Experiments were conducted on fine-grained (< 15 µm) aggregates of natural andalusite, kyanite and sillimanite at 1250 °C, 300 MPa, and a constant shear strain rate of 2 × 10− 4/s to a maximum shear strain of 400%. Electron back-scattered diffraction (EBSD) analysis of the experiments revealed development of lattice-preferred orientations, with alignment of sillimanite and andalusite [001] slightly oblique to the shear plane. The kyanite experiment could not be analyzed using EBSD because of near complete transformation to sillimanite. Very little strain ( 30%) is required to produce widespread transformation in kyanite and andalusite. Polymorphic transformation in andalusite and kyanite experiments occurred primarily along 500 µm wide shear bands oriented slightly oblique and antithetic to the shear plane and dominated by sub-µm (100–150 nm) fibrolitic sillimanite. Shear bands are observed across the entire strain field preserved in the torsion samples. Scanning transmission electron microscope imaging shows evidence for transformation away from shear bands; e.g. fibrolitic rims on relict andalusite or kyanite. Relict grains typically have an asymmetry that is consistent with shear direction. These experimental results show that sillimanite is by far the weakest of the polymorphs, but no distinction can yet be made on the relative strengths of kyanite and andalusite. These observations also suggest that attaining high bulk strain energy in strong materials such as the Al2SiO5 polymorphs is not necessary for triggering transformation. Strain energy is concentrated along grain boundaries, and transformation occurs by a dynamic recrystallization type process. These experiments also illustrate the importance of grain-size sensitive creep at high strains in a system with simultaneous reaction and deformation.  相似文献   

14.
EH pH diagrams have been calculated using the PHREEQC programme in order to establish the predominance fields of Mn, Fe, Co, Ni, Cu and As in bottom waters from the Angola Basin. Predominance fields are presented separately for both aquatic species and solid mineral phases in order to simplify interpretation of the data. The diagrams show significant differences from standard EH pH diagrams for these elements calculated for freshwater at 25 °C and 1 bar which assume an element concentration of 10-6 M. In particular, our diagrams show that Mn2+ and NiCO 3 0 are the predominant aquatic species for Mn and Ni in bottom seawater and FeOOH, Fe2O3, Fe3O4, CoFe2O4, CuFe2O4, CuFeO2, and Ba3 (AsO4)2 the predominant solid phases for Fe, Co, Cu and As, respectively. Mn and Ni are therefore undersaturated and Fe, Co, Cu and As supersaturated in bottom seawater from the Angola Basin. Neither rhodochrosite (MnCO3) nor siderite (FeCO3) can form in this marine environment in equilibrium with seawater. A mixed Mn-Ca carbonate is therefore formed within the pore waters of reducing sediments. The high Ni/Cu ratios in cobalt-rich manganese crusts formed adjacent to the oxygen minimum zone may be explained by the change from Cu2+ to CuCl 3 2- as the dominant aquatic species of Cu in seawater at an EH of +0.48 V.  相似文献   

15.
Otavite, witherite, calcite, strontianite, hydrozincite and hydrocerussite nucleation was induced by CO2 diffusion through a polyethylene membrane into a metal bearing solution. Nucleation and ongoing precipitation was followed at 25 ± 1 °C by the chemical evolution of the solution and the consumption of sodium hydroxide (pH-stat conditions). X-ray diffraction patterns as well as FT-infrared and Raman spectra confirmed the formation of well crystallized solids, except for less crystalline hydrozincite. In several experiments simonkolleite and laurionite precipitated concurrently with hydrozincite and hydrocerussite. The carbonate end-member minerals, smithsonite and cerussite, however were not formed. Carbonate minerals crystallized as spherical aggregates of thin layered otavite, spherical orientated witherite needles, rhombohedral calcite, pseudo-hexagonal strontianite laths, fibrous lumps of hydrozincite and planar hexagonal hydrocerussite crystals. Crystal and aggregate sizes range between 1 and 100 μm. Nucleation occurred at well defined reaction times and distinct critical supersaturation indices (SIcrit). The time for nucleation at constant pH decreased as the initial metal concentration increased for a given solid. The SIcrit values decreased in the order of hydrocerussite (3.2), otavite (2.5), strontianite (1.6), witherite (0.9) and calcite (0.7).  相似文献   

16.
In the Sanandaj-Sirjan zone of metamorphic belt of Iran, the area south of Hamadan city comprises of metamorphic rocks, granitic batholith with pegmatites and quartz veins. Alvand batholith is emplaced into metasediments of early Mesozoic age. Fluid inclusions have been studied using microthermometry to evaluate the source of fluids from which quartz veins and pegmatites formed to investigate the possible relation between host rocks of pegmatites and the fluid inclusion types. Host minerals of fluid inclusions in pegmatites are quartz, andalusite and tourmaline. Fluid inclusions can be classified into four types. Type 1 inclusions are high salinity aqueous fluids (NaCleq >12 wt%). Type 2 inclusions are low to moderate salinity (NaCleq <12 wt%) aqueous fluids. Type 3 and 4 inclusions are carbonic and mixed CO2-H2O fluid inclusions. The distribution of fluid inclusions indicate that type 1 and type 2 inclusions are present in the pegmatites and quartz veins respectively in the Alvand batholith. This would imply that aqueous magmatic fluids with no detectable CO2 were present during the crystallization of these pegmatites and quartz veins. Types 3 and 4 inclusions are common in quartz veins and pegmatites in metamorphic rocks and are more abundant in the hornfelses. The distribution of the different types of fluid inclusions suggests that CO2 fluids generated during metamorphism and metamorphic fluids might also contribute to the formation of quartz veins and pegmatites in metamorphic terrains.  相似文献   

17.
高锰酸盐指数(CODMn)、硝酸根(NO-3)、铵根(NH+4)是判断水体是否受到三氮污染的重要指标。对于测定这三个指标的水样保存方式和时间,地质行业标准和国内外主要国家标准间存在明显差异。地质行业标准规定地下水样品原水室温保存,CODMn和NH+4在3天内测定;NO-3在20天内测定;国家标准和美国标准推荐样品硫酸酸化,避光或冷藏保存,在2~7天内完成CODMn和NO-3和1~7天内完成NH+4测试。为了分析各类标准在样品保存要求上的差异对检测结果的影响,确保检测数据能真实地反映水体污染状况,找寻简便的保存方式,本文在广州地区采集地下水,按照地质行业标准与国家标准进行处理和保存,并在不同时间段对三个指标进行测试。分析验证结果表明:地质行业标准与国家和美国标准关于水样的保存方法均非常可靠。地质行业标准主要针对静态地下水,保存方法相对宽松;国家标准和美国标准适用范围除了地下水,还包括动态的地表水和废水,采样对象成分更为复杂,更不稳定,更容易受外界影响发生变化,故保存条件高于地质标准。在广州地区,采用原水室温避光保存水样,CODMn、NH+4保存时间可为5天,NO-3保存时间可为30天;采用酸化水室温保存水样,CODMn、NO-3和NH+4保存时间可长达30天。这两种方式均比地质行业标准和国家标准推荐的有效时间长,且原水和酸化水室温保存方式相对于冷藏保存方式更为方便。本文提出,如果采集的水样能方便、快速送达实验室,可采用原水保存;如果不能在短时间内送达实验室检测,可采用硫酸酸化保存。  相似文献   

18.
We report here a single-crystal polarized-light study of stoppaniite, ideally (Fe,Al,Mg)4(Be6Si12O36)(H2O)2(Na,□), from Capranica (Viterbo). Polarized-light FTIR spectra were collected on an oriented (hk0) section, doubly polished to 15 μm. The spectrum shows two main bands at 3,660 and 3,595 cm−1; the former is strongly polarized for E ⊥c, while the latter is polarized for E //c. A sharp and very intense band at 1,620 cm−1, plus minor features at 4,000 and 3,228 cm−1 are also polarized for E //c. On the basis of literature data and considering the pleochroic behavior of the absorptions, the 3,660 cm−1 band is assigned to the ν3 stretching mode and the 1,620 cm−1 (associated with an overtone 2*ν2 at 3,230 cm−1) band to the ν2 bending mode of “type II” water molecules within the structural channels of the studied beryl. The sharp band at 3,595 cm−1 is not associated with a corresponding ν2 bending mode; thus it is assigned to the stretching vibration of O–H groups in the sample. The minor 4,000 cm−1 feature can be assigned to the combination of the O–H bond parallel to c with a low-frequency metal-oxygen mode such as the Na–O stretching mode. The present results suggest that the interpretation of the FTIR spectrum of Na-rich beryl needs to be carefully reconsidered.  相似文献   

19.
Baghdadite from Fuka, Okayama Prefecture, Japan shows a bright yellow fluorescence under UV (Hg 253.7 nm) excitation. The photoluminescence (PL) spectrum at 300 K consists of one large band near 580 nm and two small UV bands at 318 and 397 nm. The optical excitation spectrum of the bright yellow fluorescence consists of two bands near 220 and 250 nm. The temperature dependence of the PL intensity exhibits linear thermal quenching. To reveal the origin of the bright yellow fluorescence from baghdadite, powder Ca3(Zr,Ti)Si2O9 crystals are synthesized. Synthetic Ca3(Zr,Ti)Si2O9 shows luminescence spectra similar to those of baghdadite, and the intensity of the yellow fluorescence is markedly increased by titanium addition. The origin of the bright yellow fluorescence from baghdadite is ascribed to the existence of titanium.  相似文献   

20.
The high-pressure behavior of a vanadinite (Pb10(VO4)6Cl2, a = b = 10.3254(5), c = 7.3450(4) Å, space group P63/m), a natural microporous mineral, has been investigated using in-situ HP-synchrotron X-ray powder diffraction up to 7.67 GPa with a diamond anvil cell under hydrostatic conditions. No phase transition has been observed within the pressure range investigated. Axial and volume isothermal Equations of State (EoS) of vanadinite were determined. Fitting the P–V data with a third-order Birch-Murnaghan (BM) EoS, using the data weighted by the uncertainties in P and V, we obtained: V 0 = 681(1) Å3, K 0 = 41(5) GPa, and K′ = 12.5(2.5). The evolution of the lattice constants with P shows a strong anisotropic compression pattern. The axial bulk moduli were calculated with a third-order “linearized” BM-EoS. The EoS parameters are: a 0 = 10.3302(2) Å, K 0(a) = 35(2) GPa and K′(a) = 10(1) for the a-axis; c 0 = 7.3520(3) Å, K 0(c) = 98(4) GPa, and K′(c) = 9(2) for the c-axis (K 0(a):K 0(c) = 1:2.80). Axial and volume Eulerian-finite strain (fe) at different normalized stress (Fe) were calculated. The weighted linear regression through the data points yields the following intercept values: Fe a (0) = 35(2) GPa for the a-axis, Fe c (0) = 98(4) GPa for the c-axis and Fe V (0) = 45(2) GPa for the unit-cell volume. The slope of the regression lines gives rise to K′ values of 10(1) for the a-axis, 9(2) for the c-axis and 11(1) for the unit cell-volume. A comparison between the HP-elastic response of vanadinite and the iso-structural apatite is carried out. The possible reasons of the elastic anisotropy are discussed.  相似文献   

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