192 resultados para N2 atmospheres
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In the Bi-based high-T(c) superconductors, three superconducting transition points were observed above the liquid-N2 temperature range. Allotropes of the 2212 phase were found. These allotropes were metastable and can interchange with the 2212 phase, and their T(c)'s vary from approximately 85 to approximately 100 K.
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MoO3/Al2O3 is reduced at least partly by sulfur which is formed from H2S in sulfidation with H2S/N2 mixture. SO2 formation during TPD of MoO3/Al2O3 with presorbed H2S provides evidence for the explanation.
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研究了三甲基硅烷基丙块与五甲基二硅烷基丙块共聚物〔poly(TMSP-co-PMDSP)〕的成膜特点。poly(TMSP-co-PMDSP)膜的气体透过系数分别为:P_(O2):4×10~3~12×10~3,P_(N2):3×10~3~8×10~3和P_(CO2):2×10~4~4×10~4barrer,气体透过稳定性低,透过行为偏离第二Fick定律,过系数下降,其中溶解系数降低的比例远大于扩散系数的增加比例,在含有凝聚性气体的环境里,膜的气体透过出现表面吸附控制的特征。
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本文分别以 KAlF_4:Eu~(2+)和 RbGaF_4:Eu~(2+)为例,讨论了碱金属—镓族复合氟化物中 Eu~(2+)发射中心形成的过程。合成了掺 Eu~(2+)的 AMF_4(A=Na,K,Rb,Cs,M=B,Al,Ga)及 AI_(n2)F_7(A=K,Rb)。Eu~(2+)占据 AMF_4中 A~+格位。AMF_4:Eu~(2+)和 AI_nF_7:Eu~(2+)中,Eu~(2+)发射是锐峰,来源于 f→f 跃迁。Eu~(2+)进入取代格位形成发射中心的过程与中间产物(A_4MF_(?))和激活剂(EuF_2)分解条件有关。由于4f 电子受到良好屏蔽,Eu~(2+)的 f→f 发射峰位置不变。
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The dynamic process of the ionic valence changing from Eu~(2+) to Eu~(3+) in EuF_2 at high temperature has been investigated by ESCA, high,temperature X-ray diffraction, high temperature spectrum, high temperature magnetic Isusceptibility and Mssbauer spectrum. It has been shown that the formed Eu~(3+) exists in different compounds when EuF_2 is heated to high temperature in different atmospheres. In air, Eu~(3+) exists in the form of hexagonal EuOF, in nitrogen, in the form of orthogonal EuF_3 and non-hexa...
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本论文旨在利用free-drift 开放反应系统,保持反应系统温度和二氧化碳分压(pCO2)恒定,研究人工海水中文石、方解石在近溶解、沉淀平衡状态下溶解、沉淀动力学过程,分析pCO2的变化对文石、方解石溶解和沉淀速率及其动力学方程的影响,探讨不同饱和度条件下文石和方解石之间溶解/沉淀速率的关系。 绝大部分实验温度控制在25℃,为了探讨温度对溶解速率及其动力学的影响,小部分实验在15℃环境下进行。根据反应过程中,反应液碳酸盐碱度值随时间的变化,计算文石、方解石的溶解、沉淀速率。通过改变实验中通入CO2/N2混合气体的pCO2(0/300/3000ppm),探讨pCO2 对海洋中碳酸盐沉淀、溶解机制的影响。 在相同的温度、pCO2、饱和度(Ω)条件下,如果Ω < 0.75,文石的溶解速率大于方解石;当Ω > 0.8 时,方解石的溶解速率小于文石。温度和饱和度相同时,pCO2越高,文石和方解石的溶解速率越大,但对沉淀速率没有明显的影响。
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本文依据收集到的392个地面验潮站8个主要分潮(M2、S2、K1、O1、N2、K2、P1及Q1)的调和常数,对现有7个全球大洋潮汐模式的准确度进行了检验,结果显示各模式在深海区域均达到了比较高的准确度,相互之间差别也不大。经验模式GOT00和CSR4.0、同化模式NAO99、反演同化模式TPXO7.0、数值同化模式FES2002和FES2004的M2分潮均方根偏差在3 cm左右,其它分潮(S2、K1、O1、N2、K2、P1及Q1)大约在1~2 cm。本文还依据中国近海18个岛屿的调和常数对其中的5个大洋潮汐模式的准确度进行了检验,结果表明,M2分潮均方根偏差在6~14 cm,明显高于大洋部分的偏差,其中日本国家天文台的潮汐模式NAO99在中国近海的结果相对较准确。 我们利用1992年8月至2008年8月的TOPEX/POSEIDON和JASON-1(T/P-J)卫星高度计资料,对沿卫星轨道的302816个站点进行了14个分潮的潮汐调和分析,得到了全球大洋潮汐的8个主要分潮以及2个气象分潮Sa、Ssa的经验同潮图。主要结果有:(1)各分潮在卫星上升轨道与下降轨道的交叉点(约7000个)相关性分析表明:M2分潮的振幅和迟角的相关系数很高(分别为0.9965和0.9961);S2,K1,O1和Sa分潮也有较好的相关性(相关系数为0.94~0.99);(2)该结果与392地面个验潮站吻合较好,其中M2分潮的振幅、迟角和向量的均方根偏差分别为:1.73 cm,2.340和2.93 cm;S2,K1和O1分潮的振幅、迟角和向量的均方根偏差为1 cm左右,5.250~7.270和1.5~2.1 cm,该精度与最近几年国际上的主要大洋潮汐模式的准确度相近;(3)首次通过卫星资料获得了Sa、Ssa分潮的同潮图。周期为1年的Sa分潮与大洋105个地面站相比,振幅、迟角和向量的均方根偏差分别为1.50 cm、18.360和2.16 cm。在此基础上,进一步分析了构成Sa、Ssa气象分潮的两个主要因素(海水密度以及海面气压)在全球的分布。 在T/P-J等卫星资料无法覆盖到南大洋和北冰洋,本文利用Princeton Ocean Model(POM)进行了数值模拟,模拟结果与162个地面实测站(其中南大洋30个,北冰洋132个)的观测比较一致。基于卫星资料分析的结果和数值模拟结果合并得到了全球大洋的8个主要分潮同潮图。在此基础上通过全球潮汐能量耗散的计算得到潮能通量的分布,并得到全球M2、S2、K1和O1分潮的潮汐能量耗散率为2.431TW、0.401TW、0.336TW和0.176TW。 本文还利用卫星资料对南海潮汐进行了研究,在中国南海,获得了主要的半日潮、全日潮、四分日分潮和长周期分潮(M2,S2,N2,K2,K1,O1,P1,Q1,M4, MS4,Sa, Ssa)的经验同潮图。与南海沿岸94个地面验潮站的数据符合得比较好,M2,S2,K1及O1等4个主要分潮的平均振幅差为2~4 cm,均方根偏差分别是9~11 cm.其它4个主要分潮N2,K2,P1,Q1的平均振幅差为1~2 cm,均方根偏差为2~4 cm。此外,本文还利用卫星高度计资料潮汐分析结果沿卫星轨道进行高通滤波,分离得出中国近海的M2,S2,K1及O1分潮的内潮信息。
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利用X射线衍射仪(XRD)、透射电子显微镜(TEM)、高分辨率透射电子显微镜(HRTEM)、X射线能谱仪(EDS)、选区电子衍射(SAED)、傅立叶红外变换光谱仪(FTIR)、比表面及孔径分析仪(SAA, N2-BET)等手段对来自北太平洋的深海粘土沉积物组份及其CTMAB/DTAB有机复合体进行表征,并对照研究了其对苯胺、苯酚及对氨基苯磺酸溶液的吸附行为。研究结果表明,CTMAB/DTAB有机阳离子随机进入可膨胀类矿物层间并使其有效层间域增大。XRD、HRTEM及FTIR可提供有机分子进入层间的直接证据。HRTEM及SAED研究显示,有机复合体的晶体结构未发生改变,但出现了更多的活性中心。在不同密度堆积状态下,有机阳离子在层间的排列方式存在差异。N2-BET的相关研究表明有机粘土复合体的外比表面积较原土有不同程度的减小,但介孔比表面积和总体积较原土有所增加,且孔径有集中分布的趋势。等温吸附——脱附曲线上的B类滞后回环揭示深海粘土及其有机复合体含有丰富的介孔,且具平行壁狭缝状结构。吸附实验表明,有机复合体的吸附性能较原土有很大提高。在不大于5倍CEC的条件下,深海粘土复合体对实验浓度范围内的有机污染物的去除能力随有机阳离子负载量的增大而加强,且对极性溶液的吸附能力远大于非极性溶液。有机深海粘土沉积物组份对目标污染物吸附性能的提高可归结为因有机相的加入而增强的线性分配作用和大于有效孔径的孔隙的增多而加强的对目标污染物的截留效应。0.34nm可以视为吸附剂(深海粘土)截留具有单个苯环的有机污染物的最小有效孔径。相比较,硅质粘土型有机粘土复合体的环境属性优于含硅质粘土型有机粘土复合体。
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To characterize evapotranspiration (ET) over grasslands on the Qinghai-Tibetan Plateau, we examined ET and its relevant environmental variables in a Kobresia meadow from 2002 to 2004 using the eddy covariance method. The annual precipitation changed greatly, with 554, 706, and 666 mm a(-1) for the three consecutive calendar years. The annual ET varied correspondingly to the annual precipitation with 341, 407, and 426 mm a(-1). The annual ET was, however, constant at about 60% of the annual precipitation. About 85% annual ET occurred during the growing season from May to September, and the averaged ET for this period was 1.90, 2.23, and 2.22 mm/d, respectively for the three consecutive years. The averaged ET was, however, very low (< 0.40 mm/d) during the nongrowing season from October to April. The annual canopy conductance (gc) and the Priestley-Taylor coefficient (a) showed the lowest values in the year with the lowest precipitation. This study first demonstrates that the alpine meadow ecosystem is characterized by a low ratio of annual ET to precipitation and that the interannual variation of ET is determined by annual precipitation.
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We measured the net ecosystem CO2 exchange (NEE) in an alpine meadow ecosystem (latitude 37degrees29'-45'N, longitude 101degrees12'-23'E, 3250 m above sea level) on the Qinghai-Tibetan Plateau throughout 2002 by the eddy covariance method to examine the carbon dynamics and budget on this unique plateau. Diurnal changes in gross primary production (GPP) and ecosystem respiration (R-e) showed that an afternoon increase of NEE was highly associated with an increase of R-e. Seasonal changes in GPP corresponded well to changes in the leaf area index and daily photosynthetic photon flux density. The ratio of GPP/R-e was high and reached about 2.0 during the peak growing season, which indicates that mainly autotrophic respiration controlled the carbon dynamics of the ecosystem. Seasonal changes in mean GPP and R-e showed compensatory behavior as reported for temperate and Mediterranean ecosystems, but those of GPP(max) and R-emax were poorly synchronized. The alpine ecosystem exhibited lower GPP (575 g C m(-2) y(-1)) than, but net ecosystem production (78.5 g C m(-2) y(-1)) similar to, that of subalpine forest ecosystems. The results suggest that the alpine meadow behaved as a CO2 sink during the 1-year measurement period but apparently sequestered a rather small amount of C in comparison with similar alpine ecosystems.
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[1] The alpine meadow ecosystem on the Qinghai-Tibetan Plateau may play a significant role in the regional carbon cycle. To assess the CO2 flux and its relationship to environmental controls in the ecosystem, eddy covariance of CO2, H2O, and energy fluxes was measured with an open-path system in an alpine meadow on the plateau at an elevation of 3,250 m. Net ecosystem CO2 influx (Fc) averaged 8.8 g m(-2) day(-1) during the period from August 9 to 31, 2001, with a maximum of 15.9 g m(-2) day(-1) and a minimum of 2.3 g m(-2) day(-1). Daytime Fc averaged 16.7 g m(-2) day(-1) and ranged from 10.4 g m(-2) day(-1) to 21.7 g m(-2) day(-1) during the study period. For the same photosynthetic photon flux density (PPFD), gross CO2 uptake (Gc) was significantly higher on cloudy days than on clear days. However, mean daily Gc was higher on clear days than on cloudy days. With high PPFD, Fc decreased as air temperature increased from 10degreesC to 23degreesC. The greater the difference between daytime and nighttime air temperatures, the more the sink was strengthened. Daytime average water use efficiency of the ecosystem (WUEe) was 8.7 mg (CO2)(g H2O)(-1); WUEe values ranged from 5.8 to 15.3 mg (CO2)(g H2O)(-1). WUEe increased with the decrease in vapor pressure deficit. Daily albedo averaged 0.20, ranging from 0.19 to 0.22 during the study period, and was negatively correlated with daily Fc. Our measurements provided some of the first evidence on CO2 exchange for a temperate alpine meadow ecosystem on the Qinghai-Tibetan Plateau, which is necessary for assessing the carbon budget and carbon cycle processes for temperate grassland ecosystems.
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Natural fluids with water-salt-gas are often found in every sphere of the Earth, whose physicochemical properties and geochemical behaviors are complicated. To study these properties and behaviors turns out to be one of the challenging issues in geosciences. Traditional approaches mainly depend on experiments and observations. However, it is impossible to obtain a large number of data covering a large T-P space of the Earth by experimental methods in the near future, which will hinder the advance of the theoretical study. Therefore, it is important to model natural fluids by advanced theoretical methods, by which limited experimental data can be extended to a large temperature-pressure-composition space. Physicochemical models developed in this dissertation are not only more accurate, but also extend the applied T-P-m region of the experimental data of the multi-fluid systems by about two times. These models provide the new and accurate theoretical tools for the geochemical research, especially for the water-rock interactions and the study of the fluid inclusions. The main achievements can be summarized as follows: (1) A solubility model on components of natural gases is presented. The solubility model on the systems of CH4-H2O-NaCl, C2H6-H2O-NaCl or N2-H2O-NaCl takes advantage of modern physicochemical theory and methods, and is an improvement over previous models whose prediction and precision are relatively poor. The model can predict not only the gas solubility in liquid phase but also water content in the gas phase. In addition, it can predict gases (methane or nitrogen) solubility in seawater and brine. Isochores can be determined, which are very important in the interpretation of fluid inclusions. (2) A density model on common aqueous salt solutions is developed. The density models with high precision for common aqueous salt solutions (H2O-NaCl, H2O-LiCl, H2O-KCl, H2O-MgCl2, H2O-CaCl2, H2O-SrCl2 or H2O-BaCl2) are absent in the past. Previous density models are limited to the relatively small range of experimental data, and cannot meet the requirement of the study of natural fluids. So a general density model of the above systems is presented by us based on the international standard density model of the water. The model exceeds the other models in both precision and prediction. (3) A viscosity model on common aqueous alkali-chloride solutions is proposed. Dynamic viscosity of water-salt systems, an important physics variable, is widely used in three-dimension simulation of the fluids. But in most cases, due to the lack of viscosity models with a wide T-P range, the viscosity of aqueous salt solutions is replaced by that of the water, giving rise to a relatively large uncertainty. A viscosity model with good prediction for the systems (H2O-NaCl, H2O-LiCl or H2O-KCl) is presented on the base of the international standard viscosity model of water and the density model developed before. (4) Equation of State applied in fluid inclusions. The best Equations of State in the world developed by others or us recently are applied in the study of the fluid inclusions. Phase equilibria and isochores of unitary system (e.g. H2O, CO2, CH4, O2, N2, C2H6 or H2S), binary H2O-NaCl system and ternary H2O-CH4-NaCl system are finished. From these programs and thermodynamic equations of coexisting ores, the physicochemical conditions before or after the deposits form can be determined. To some extent, it is a better tool.
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Pyrite is the most stable iron-sulfide in reduced environment, and plays an important role in geochemical iron-sulfur cycling of sediments. Thus, the presence of pyrite in sediments and rocks is an important indicator of sedimentary environments. Previous studies on the thermal products of pyrite showed that all of the products (e.g., pyrrhotite, magnetite, hematite) have strong capability of carrying remanence. To deepen our understanding of the environmental and paleomagnetic significances of pyrite, the mineral transformation processes of pyrite upon heating were systematically investigated in this study using intergrated rock magnetic experiments (in both argon and air atmospheres) and X-ray diffraction analysis. The room temperature susceptibility of the paramagnetic pyrite is about 2.68×10-5 SI. In argon atmosphere (reducing environment), pyrite was transformed into monoclinic stable single domain (SD) pyrrhotite above 440 C. The corresponding coercive force and remanence coercivity are about 20 mT and 30 mT, respectively. In contrast, in air atmosphere (oxidation environment), the intermediate thermal products of pyrite are magnetite and pyrrhotite, which were quickly further oxidated to SD hematite, which has coercivity of about 1400 mT. In addition, the hematite particles gradually grow from SD to PSD grain size region by multiple heating runs. The transformation processes of pyrite in oxidation atomosphere can be interpreted by three possible pathways: (1) pyrite→magnetite→hematite; (2) pyrite→pyrrhotite→magnetite→hematite; and (3) pyrite→pyrrhotite→hematite. Low-temperature magnetic experiments show no transitions for pyrite. Despite that low-temperature magnetic method is not suitable for identification of pyrite, it is clear in this study that the high-temperature thermomagnetic measurements (e.g., -T and J-T curves) are very sensitive to the presence of pyrite in sediments and rocks. Nevertheless, for the thermal treatment products, low-temperature magnetic measurements showed the 34 K transition of pyrrhotite and the 250 K Morine transition of hematite. Iron-sulfide has also been found on Martian meteorolites by other workers. Therefore, systematic study of rock magnetism of pyrite (and other iron-sulfides) and their products will have great significances for both paleomagnetism and planetary magnetism.
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With the variations of solar activity, solar EUV and X-ray radiations change over different timescales (e.g., from solar cycle variation to solar flare burst). Since solar EUV and X-ray radiations are the primary energy sources for the ionosphere, theirs variations undoubtedly produce significant and complicated effects on the ionosphere. So the variations of solar activity significantly affect the ionosphere. It is essential for both ionospheric theory and applications to study solar activity effects on the ionosphere. The study about solar activity variations of the ionosphere is an important part of the ionospheric climatology. It can enhance the understanding for the basic processes in the ionosphere, ionospheric structure and its change, ionosphere/thermosphere coupling, and so on. As for applications, people need sufficient knowledges about solar activity variations of the ionosphere in order to improve ionospheric models so that more accurate forecast for the ionospheric environments can be made. Presently, the whole image about the modalities of ionospheric solar activity variations is still unknown, and related mechanisms still cannot be well understood. This paper is about the effects of the 11-year change in solar activity to the low- and mid-latitude ionosphere. We use multi-type ionospheric observations and model to investigate solar activity effects on the electron density and ionospheric spatial structure, and we focus on discussing some related mechanisms. The main works are as follows: Firstly, solar activity variations of ionospheric peak electron density (NmF2) around 1400 LT were investigated using ionosonde observations in the 120°E sector. The result shows that the variation trend of NmF2 with F107 depends on latitudes and seasons. There is obvious saturation trend in low latitudes in all seasons; while in middle latitudes, NmF2 increases linearly with F107 in winter but saturates with F107 at higher solar activity levels in the other seasons. We calculated the photochemical equilibrium electron density to discuss the effects induced by the changes of neutral atmosphere and dynamics processes on the solar activity variations of NmF2. We found that: (1) Seasonal variation of neutral atmosphere plays an important role in the seasonal difference of the solar activity variations of NmF2 in middle latitudes. (2) Less [O]/[N2] and higher neutral temperature are important for the saturation effect in summer, and the increase of vibrational excited N2 is also important for the saturation effect. (3) Dynamics processes can significantly weaken the increase of NmF2 when solar activity enhances, which is also a necessary factor for the saturation effect. Secondly, solar activity variations of nighttime NmF2 were investigated using ionosonde observations in the 120°E sector. The result shows that the variation trends of NmF2 with F107 in nighttime are different from that in daytime in some cases, and the nighttime variation trends depend on seasons. There is linear increase trend in equinox nighttime, and saturation trend in summer nighttime, while the increase rate of NmF2 with F107 increases when solar activity enhances in winter nighttime (we term it with “amplification trend”). We discussed the possible mechanisms which affect the solar activity variations of nighttime NmF2. The primary conclusions are as follows: (1) In the equatorial ionization anomaly (EIA) crest region, the plasma influx induced by the pre-reversal enhancement (PRE) results in the change of the variation trend between NmF2 and F107 from “saturation” to “linear” after sunset in equinoxes and winter; while the recombination process at the F2-peak is the primary factor that affects the variation trend of NmF2 with F107 in middle latitudes. (2) The recombination coefficient at the F2-peak height reaches its maximum at moderate solar activity level in winter nighttime, which induces NmF2 attenuates more quickly at moderate solar activity level. This is the main reason for the amplification trend. (3) The change of the recombination process at the F2-peak with solar activity depends on the increases of neutral parameters (temperature, density et al.) and the F2-peak height (hmF2). The seasonal differences in the changes of neutral atmosphere and hmF2 with solar activity are the primary reasons for the seasonal difference in the variation trend of nighttime NmF2 with F107. Finally, we investigated the solar activity dependence of the topside ionosphere in low latitudes using ROCSAT-1 satellite (at 600 km altitude) observations. The primary results and conclusions are as follows: (1) Latitudinal distribution of the plasma density is local time, seasonal, and solar activity dependent. In daytime, there is a plasma density peak at the dip equator. The peak is obviously enhanced at high solar activity level, and the strength of the peak strongly depends on seasons. While at sunset, two profound plasma density peaks (double-peak structure) are found in solar maximum equinox months. (2) Local time dependence of the latitudinal distribution is due to the local time variation of the equatorial dynamics processes. Double-peak structure is attributed to the fountain effect induced by strong PRE. Daytime peak enhances with solar activity since the plasma density increases with solar activity more strongly at the dip equator due to the equatorial vertical drift, and its seasonal dependence is mainly due to the seasonal variations of neutral density and the equatorial vertical drift. In the sunset sector, seasonal and solar activity dependences of the latitudinal distribution are related to the seasonal and solar activity variations of PRE. (3) The variation trend of the plasma density with solar activity shows local time, seasonal, and latitudinal differences. That is different from the changeless amplification trend at the DMSP altitude (840 km). Profound saturation effect is found in the dip equator region at equinox sunset. This saturation effect in the topside ionosphere is realated to the increase of PRE with solar activity. Solar activity variation trend of the topside plasma density was discussed quantitatively by Chapman-α function. The result shows that the effect induced by the change of the scale height is dominant at high altitudes; while the variation trend of ROCSAT-1 plasma density with solar activity is suggested to be related to the changes of the peak height, the scale height, and the peak electron density with solar activity.
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瑶岗仙钨矿区地处南岭中段,位于加里东隆起带与印支-燕山凹陷带的交汇地带。为了更深入地研究瑶岗仙钨矿成矿流体的性质和演化,在前人工作的基础上,本文结合流体包裹体的岩相学特征及其产出的构造特征,对瑶岗仙钨矿流体包裹体进行了显微测温和激光拉曼探针分析,从而确定了瑶岗仙钨矿成矿流体的性质,并进一步探讨了其成矿物质来源及成矿机制。 对瑶岗仙石英脉型钨矿床的石英、萤石和矽卡岩型钨矿床中石榴子石流体包裹体的岩相学特征研究表明,与成矿有关的包裹体主要有三类:富液相、富气相和含子晶多相包裹体。脉型钨矿床中石英的包裹体均一温度范围 180℃~300℃,盐度为 0.88~6.45 wt% NaCl;矽卡岩钨矿床中石榴子石包裹体均一温度范围为 190~300 ℃,盐度为 0.1~8.95 wt% NaCl,成矿溶液的密度为 0.70~1.05 g/cm3,说明形成两种类型矿床的流体均属中温、低密度、低盐度流体;两类矿床形成的压力为 32~38 MPa,成矿深度为 1~2 km,因此该矿床是在浅成、低压条件下形成的。激光拉曼探针测试表明,石榴石包裹体的气相成分以 H2O 为主,石英中包裹体的气相成分及其相对含量为 H2O>CO2>CH4>N2>H2S。由此说明,从矽卡岩型白钨矿阶段到石英脉型黑钨矿阶段,成矿流体中不断有 CH4、CO2和H2O 等挥发份的加入,此时的流体是一种介于岩浆与热液之间的过渡性流体,具有上部偏液、下部偏浆的特点。 根据前人的研究结果以及矿脉中花岗岩角砾的发现,泥盆系、寒武系岩层在花岗岩浆侵入过程中发生了混合岩化,成为成矿物质来源的基础,而真正的成矿母岩应该是深部的花岗岩体,由此推测“赋矿花岗岩并非成矿源岩”,很可能来自深部母岩浆中熔离出的流体。而 CH4 等还原组分的含量增多,推测也有可能来自相对是还原环境的地幔过渡带或软流圈中。