共查询到20条相似文献，搜索用时 109 毫秒
1.
2.
海洋上空颗粒物(即海洋气溶胶)体系组成和来源非常复杂,它对于大气颗粒物总数贡献非常大,是大气科学及全球变化领域研究的重要组成部分。与传统离线滤膜采样技术相比,气溶胶质谱技术具有灵敏度高、检测效率高、时空分辨率高等特点,已广泛应用于大气细颗粒物的特征和来源判别研究中。综述比较了目前应用最广泛的气溶胶质谱仪(AMS)和气溶胶飞行时间质谱仪(ATOFMS)在岛屿、沿海城市、近海、开阔大洋及南北极地等区域细颗粒物特征的研究进展。指出2种一起联合使用,可以较为全面地观测海洋气溶胶的粒径、化学组分及混合态的特征,为中国近海的雾霾监测网建设和治理空气污染提供一定的科学依据。 相似文献
3.
页岩含气量的确定是页岩气储层评价和资源量评估的一项基础内容为含气量的确定。在调研国内外文献的基础上,对直接解吸法测定页岩含气量的实验原理和方法及易产生误差的损失气量的确定方法进行讨论分析,结果认为损失时间的长短、损失段的解吸速率以及算法模型的选择对损失气量估算结果有重大影响,要准确确定损失气量需利用更高分辨率解吸测试仪器,正确认识解吸速率随时间,温压条件改变的规律,提出在USBM法的理论基础上利用实验数据分阶段(密闭取心+地面逸散)逐步拟合回归,求取损失气量。 相似文献
4.
5.
6.
独立封存的单个流体包裹体,能够准确地反演被捕获时期的流体信息.激光剥蚀电感耦合等离子体质谱仪（LA-ICP-MS）是单个流体包裹体微区分析的重要手段,展现了原位、实时、高空间分辨率、高灵敏度、高精密度、低检出限、多元素同时检测的优点.单个流体包裹体组成信息的LA-ICP-MS测定技术,在单个流体包裹体选取、激光剥蚀采样方式、气溶胶传输与电离、质谱瞬时信号采集效率、定量校准与内标元素准确测定等方面逐步突破,且该技术应用于成矿元素来源及分配、成矿流体来源及特征、建立成矿模式等方面的研究广泛.因此提高单个流体包裹体分析成功率、降低小体积流体包裹体元素检出限、测定矿石矿物流体包裹体成分等成为该分析技术亟待解决的问题. 相似文献
7.
^40Ar-^39Ar同位素定年法是由K-Ar法发展而来,通过将39K利用快中子辐照衰变成^39Ar,测量40Ar^＊/^39Ar来获得年龄值.经过长期发展,该方法的测试技术逐渐成熟,其中气体提取发展为常规阶段升温法、激光显微探针法以及真空压碎流体包裹体法;气体纯化主要有冷阱去除法、钛泵吸附法、锆铝泵吸附法;气体测试的质谱仪也在灵敏度、分辨率、背景值等技术指标上有很大提高.^40Ar-^39Ar同位素定年法在石油、固体矿产等方面应用广泛,尤其在油气成藏时间、成岩成矿作用时间的热年代学研究等领域. 相似文献
8.
常规取心过程中页岩含气量解吸测定分析及建议 总被引：1，自引：0，他引：1
我国页岩气储层埋深大,普遍采用常规取心方式。根据页岩储层条件及孔隙结构分析,解吸法可以更为准确的测定页岩含气量。统计发现,页岩气与煤层气在累计解吸气量与解吸时间的关系中比较一致,在解吸速率和解吸时间的关系中存在较大差距,因此,采用回归法计算损失气的方法不能在页岩气解吸中盲目使用,需谨慎选择稳定解吸点计算损失气。分析认为,通过三阶温度解吸分步骤计算损失气能够完善整个测定过程;同时,针对不同压力条件地层,损失时间的计算要根据实际储层压力、泥浆压力、大气压力进行计算,保障常规取心过程中损失气及页岩含气量的准确性。 相似文献
9.
孔隙压力对煤岩基质解吸变形影响的试验研究 总被引：1，自引：0，他引：1
煤层气开采过程中,伴随着煤层气不断地吸附、解吸和渗流,煤体产生变形,极易导致煤和瓦斯突出事故。以晋城天地王坡煤矿为例,通过实验室内试验,模拟煤层气在复杂地层漫长的形成和逐渐开采过程,得到了孔隙压力与解吸量、应变的变化关系,并拟合得出其相应关系表达式,揭示了一些新的规律:(1)初期解吸速度较快,解吸量随时间的增长而不断增加,后期解吸速度减缓,解吸量逐渐趋于稳定;(2)孔隙压力与解吸量、应变呈现抛物线曲线关系,随孔隙压力的升高,吸附和膨胀变形占主导,其值均在增大;(3)存在最小孔隙压力值,随孔隙压力的增大,解吸时间增长,孔隙压力越小,吸附解吸规律越不明显,对于晋城天地王坡煤矿3#煤样,该值在1.0MPa左右;(4)不同加载方式对解吸量和变形量影响较大,先部分加载吸附后全部载荷解吸结果同比加全部载荷吸附解吸结果高13%～77%。试验结果可为煤层气(CBM)抽放安全和煤与瓦斯突出防治提供理论依据。 相似文献
10.
《岩矿测试》2007,26(1):12-12
内容简介：本书全面介绍了电感耦合等离子体质谱（ICP—MS）的仪器结构和基本原理，以四极杆ICP—MS为主，同时对近年来发展的其他类型的ICP—MS仪器进行了简要介绍。以地质应用为主，介绍了几种痕量超痕量元素分析方法及应用。全书共分12章：绪论，包括ICP—MS的起源、现状与发展趋势；ICP—OMS仪器结构和基本原理；ICP—MS分析性能与基本概念；扇形磁场等离子体质谱仪；飞行时间等离子体质谱；激光剥蚀电感耦合等离子体质谱；ICP—MS中的干扰；常用的地质样品处理方法；地质样品中痕量超痕量元素分析；铂族元素分析；同位素比值分析；ICP—MS联用技术在形态分析中的应用。 相似文献
11.
Franck Humbert Guy Libourel Christian France-Lanord Laurent Zimmermann Bernard Marty 《Geostandards and Geoanalytical Research》2000,24(2):255-260
A new installation for the analysis of picomole quantities of nitrogen has been designed and constructed. It permits the simultaneous analysis of N and rare gases extracted from silicates by heating. The extraction procedure involves the use of a CO2 laser as a heater, and the analysis is made by static mass spectrometry using a high sensitivity, high resolution mass spectrometer. Procedural blanks of 2 picomoles N2 (60 picogram N) allow us to analyse routinely N in mg-sized samples such as mantle-derived and meteoritic minerals, and Lunar soil grains. 相似文献
12.
Marek Tulej Andreas Riedo Maike B. Neuland Stefan Meyer Peter Wurz Nicolas Thomas Valentine Grimaudo Pavel Moreno‐García Peter Broekmann Anna Neubeck Magnus Ivarsson 《Geostandards and Geoanalytical Research》2014,38(4):441-466
Performance studies of a microscope‐camera system (MCS) and a laser ablation/ionisation mass spectrometer (LIMS) instrument (referred to here as a laser mass spectrometer or LMS) are presented. These two instruments were designed independently for in situ analysis of solids on planetary surfaces and will be combined to a single miniature instrument suite for in situ chemical and morphological analysis of surface materials on planetary bodies. LMS can perform sensitive chemical (elemental, isotope and molecular) analyses with spatial resolution close to micrometre‐sized grains. It allows for studies with mass resolution (M/ΔM) up to 800 in ablation mode (elemental composition) and up to 1500 in desorption mode (molecular analysis). With an effective dynamic range of at least eight orders of magnitude, sensitive and quantitative measurements can be conducted of almost all elements and isotopes with a concentration larger than a few ppb atoms. Hence, in addition to the major element composition, which is important for the determination of mineralogical constituents of surface materials, trace elements can also be measured to provide information on mineral formation processes. Highly accurate isotope ratio measurements can be used to determine in situ geochronology of sample material and for investigations of various isotope fractionation processes. MCS can conduct optical imagery of mm‐sized objects at several wavelengths with micrometre spatial resolution for the characterisation of morphological surface details and to provide insight into surface mineralogy. Furthermore, MCS can help in the selection of sample surface areas for further mass spectrometric analysis of the chemical composition. Surface auto‐fluorescence measurements and images in polarised light are additional capabilities of the MCS, to identify either fluorescing minerals or organic materials, if present on the analysed surface, for further investigation by LMS. The results obtained by investigations of NIST reference materials, amino acid films and a natural graphite sample embedded in silicate rock are presented to illustrate the performance of the instruments and their potential to deliver chemical information for mineral and organic phases in their geological context. 相似文献
13.
14.
稀有气体同位素的激光探针分析:技术与应用 总被引：4，自引：0，他引：4
稀有气体同位素的激光探针分析就是利用激光的集束性和高能性来抽提固体样品中的气体 ,然后将气体净化、分离之后送入质谱计测定其含量和同位素组成。该系统主要由显微监视系统、激光发射系统、位移调节系统、样品处理系统和质谱计组成。薄片样品放入真空样品室后 ,利用显微监视系统可以对薄片进行分析和照相 ,可以对小到 30～ 5 0 μm的微小区域定位分析。该方法的优势主要在于 :(1)系统本底非常低 ;(2 )样品用量较少 ;(3)具有很高的空间分辨率 ;(4 )利用“Q开关” ,可以用作微破裂工具 ;(5 )与熔融法相比 ,分析成本较低。它也有不足之处 :(1)系统的投入成本高 ;(2 )各稀有气体的抽提效率不均一 ,需要校正。 相似文献
15.
The distributions of steroid and triterpenoid hydrocarbons in crude oils and sedimentary rock extracts can be routinely determined by the direct injection of the sample into a gas chromatograph coupled to a mass spectrometer (GC-MS). The mass spectrometer is operated at a resolution of about 2500 (10% valley), and only the ion intensities at selected accurate mass values, diagnostic of the structural types of interest, are monitored throughout the analysis. The distributions, so obtained, find application in the assessment of the source and thermal maturity of crude oil accumulations in the subsurface. This technique eliminates chromatographic separation steps and combines two analyses in one. Thus, more geological samples and reference mixtures may be analyzed in a given time. 相似文献
16.
In 1973 Bill Compston advocated the building of an ion microprobe at the Research School of Earth Sciences (RSES) at the Australian National University (ANU). The commercial ion probes available at this time were too small to have sufficient sensitivity for trace element analysis and too low in mass resolution to avoid molecular interferences. The project commenced in 1974 with the appointment of a former ANU PhD student Steve Clement who had expertise in beam transport theory. To achieve high sensitivity and high mass resolution, beam transport theory indicated that a much larger magnet than in any commercially available mass spectrometer would be required. Clement chose an ion optical design, by Professor Matsuda of Osaka University in 1974, which had the required combination of high mass resolution and high transmission. Clement's job was to produce the detailed scientific designs and machine drawings for the new instrument as well as testing the completed instrument. Clement coined the term SHRIMP-Sensitive High Resolution Ion MicroProbe. By the end of 1977 nearly all the components had been manufactured and the big electromagnet had been successfully tested. In the following year the secondary mass analyzer was assembled and tested using a thermal ionization source and showed great promise with flat-topped peaks at 5000 resolution and 50% transmission with 50 V energy spread. At this stage the machine had far exceeded the specifications for the available commercial ion probes. Continued development during 1981 to the point where the original design specifications were fully realized was time consuming since learning how to use the entirely novel instrument was no simple task; no one else had an instrument like SHRIMP. The application of the instrument to zircon U–Pb geochronology established the necessary operating conditions for measuring Pb isotopic compositions and the elemental ratios Pb/U and U/Zr from 20 μm diameter spots on single zircon grains. Application of this in the early 1980s started a revolution in Precambrian geology by the ability to produce rapidly accurate and precise age determinations on structurally complex zircon samples. 相似文献
17.
The Paraná volcanic province is a window into mantle and crustal processes in the Cretaceous. The variability and complexity of this province can be determined through the study of minerals. An integrated study of zircon from Paraná lavas (one high-Ti basalt, one low-Ti andesite, one high-Ti rhyodacite and one high-Ti andesite sill) was achieved using backscattered electron imaging, sensitive high resolution ion microprobe (SHRIMP-IIe) for U-Pb geochronology, and laser ablation inductively coupled mass spectrometer (LA-ICPMS) to determine the Lu-Hf isotopes and the trace-element compositions. U-Pb-Hf and trace-element data indicate that zircon crystallized from the magma at approximately 134 Ma. This South American large igneous province originated from the mantle and was contaminated by crust either in the mantle or during ascent and crystallization of magma. Contaminant continental crust had Precambrian age. Trace elements point to a new compositional field for zircon, different from other types of provinces. Examination of volcanic zircon improves our understanding of age and contamination of the Paraná volcanics. 相似文献
18.
A Merchantek LUV266 TM petrographic ultraviolet (UV) laser microprobe has been used in conjunction with a Finnigan MAT ELEMENT TM high resolution ICP double-focusing mass spectrometer (HR-ICP-MS) for solid microsampling and geochemical analysis. This new configuration for laser ablation has the advantage of coupling the high sensitivity and fast scanning technology applied in the ELEMENT with the ablation efficiency of a UV laser. Optimisation of the configuration on the synthetic NIST SRM 612 glass standard reference material using Q-switched UV laser energy of 2 mJ and a 5 Hz repetition rate demonstrates: (1) a linear element response factor throughout the mass spectrum, suggesting limited fractionation during laser ablation; (2) a high sensitivity and very low background noise for most elements of interest; (3) limits of detection ranging from 3 ng g-1 for Sc to 300 pg g-1 for U; (4) a flat topped peak shape suitable for precise isotopic measurements; and (5) a flat bottomed crater geometry which permits progressive ablation for the analysis of thin sections. Average precision and accuracy estimates based on replicate analyses of synthetic NIST standard reference material and USGS BCR-2G glasses are below 10% for most elements. 相似文献
19.
三种方法测试岩溶水样氢氧同位素的对比研究 总被引：1，自引：0，他引：1
通过高温热转换元素-同位素比值质谱法（TC/EA-IRMS）、多用途气体制备仪-同位素比值质谱法（GasbenchⅡ-IRMS）以及激光光谱法对岩溶水样进行对比检测,其结果显示:对于氢同位素,TC/EA-IRMS的精密度达到0.3 ‰,激光光谱法的精密度达到0.1 ‰,均优于GasbenchⅡ-IRMS的精密度1.4 ‰;对于氧同位素,GasbenchⅡ-IRMS的精密度达到0.02 ‰,激光光谱法的精密度达到0.04 ‰,优于TC/EA-IRMS的精密度0.16 ‰。使用激光光谱法测定岩溶水样的氢氧同位素,所需要的样品量少,精密度高,能够满足岩溶区样品的高精度测试要求。 相似文献
20.
Yu Liu Qiu‐Li Li Guo‐Qiang Tang Xian‐Hua Li 《Geostandards and Geoanalytical Research》2020,44(3):421-437
A combined geochronological and geochemical investigation for the same domain of zircon provides valuable information on timing and genesis, particularly in the case of multi‐growth metamorphic zircon. A high spatial resolution concurrent analytical method for zircon U‐Pb age and rare earth element content was successfully achieved in this study, using a multi‐collector secondary ion mass spectrometer (SIMS) at a ~ 8 μm diameter scale. Special instrument parameters were employed, including a high mass resolution of approximately 15000 applied to replace the previous energy filter method, and a dynamic multi‐collector mode used to reduce the measurement time to 18 min per analysis. Six zircon reference materials yielded precise and accurate 206Pb/238U ages, which are comparable to those obtained by the ordinary mono‐collector method, but with 2–3 times higher spatial resolution. All zircon grains measured in this study showed enriched heavy‐REE (HREE) contents consistent with previously reported values determined by LA and solution ICP‐MS methods. The light‐REE (LREE) mass fractions measured using both SIMS and LA‐ICP‐MS methods in this study, although with quite different volume, show consistent results within uncertainties. 相似文献