共查询到19条相似文献,搜索用时 62 毫秒
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TRITON是目前国际上顶尖的固体同位素质谱仪之一,测量准确度与分析精度优于0.0005%。由于结构复杂,线路众多,本文仅介绍磁场系统基本组成,并剖析二例典型故障,供同行参考。 相似文献
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微波等离子体炬(microwave plasma torch,MPT)具有功耗低、操作方便、结构简单等优点,与质谱仪联用可快速分析元素。本文报道了一套自制的低功耗微波等离子体炬飞行时间质谱仪(MPT-TOF MS)及进样装置,并考察了维持气流速、载气流速、超截取锥电压、MPT炬焰位置及微波功率对元素检测的影响,系统地研究了该仪器的性能。结果表明,MPT-TOF MS具有耗气量少(氩维持气流速800 mL/min、氩载气流速400 mL/min、氮干燥气流速2 000 mL/min)、离子源功耗低(100 W)的优势,且线性范围覆盖5个数量级,分辨率高,锂、钠、钾、铷和铯元素的检出限分别为0.49、3.05、1.31、0.74、0.34μg/L。该仪器可用于盐湖中锂、钠、钾、铷及铯碱金属元素的快速检测,是电感耦合等离子体质谱(ICP-MS)元素检测方法的补充。 相似文献
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离子阱质谱仪小型化的最新研究进展 总被引:2,自引:1,他引:2
为适应科技发展的需要,质谱议的小型化已成为目前分析仪器发展的一个重要趋势,其中离子阱质谱仪的小型化取得了举世瞩目的成果。离子阱的小型化是通过应用小型真空泵、小型真空系统及较低的射频电压和简化阱结构(从双曲线离子阱到圆柱型离子阱再到矩形离子阱)来实现的。和其他形式的Paul离子阱一样,在外部离子注入模式下,圆柱形离子阱具有较低的捕获效率和较低的储存容量(对于商业尺寸的离子阱只能存储大约500个离子),尤其是在低射频电压工作条件下,阱尺寸减小时更是如此。为克服这些缺点,出现了一种新的离子阱质量分析器一矩形离子阱质量分析器。本文介绍了离子阱质量分析器的小型化原理,对其最新研究进展进行了评述。 相似文献
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László Tőkés 《Mass spectrometry reviews》2017,36(4):520-542
This reminiscing review article is an account of the author's fascination and involvements with mass spectrometry from the perspective of an organic chemist with an interest in natural product chemistry. It covers a period from 1961 through the mid 1990s as mass spectrometry evolved form a novelty technique to become a most widely used analytical technique. Following a brief synopsis of my pathway to mass spectrometry, my research efforts in this field are presented with a focus mainly on evolving principles and technologies which I had personal involvements with. To provide historical perspectives, discussions of these developments are accompanied by brief outlines of the relevant state‐of‐the‐art, shedding light on the technical and conceptual challenges encountered during those early days in mass spectrometry. Examples are presented of my involvements with basic and applied research in mass spectrometry during graduate studies at Stanford University and close to three decade tenure in pharmaceutical research at Syntex Research. My basic research interests focused mainly on principles of electron ionization induced fragmentation mechanisms, with an emphasis on steroids and other model compounds. Extensive deuterium labeling evidence was used to determine the fragmentation mechanisms of the diagnostically significant ions in the spectra of numerous model compounds, uncovering examples of wide‐ranging hydrogen transfers, skeletal rearrangements, methyl and phenyl migrations, stereoselective fragmentations and low and high energy fragmentation processes. Depiction of the industrial research phase of my career includes comments on the pivotal role mass spectrometry played on advancing modern pharmaceutical research. Examples are presented of involvements with instrumental developments and a few select cases of applied research, including studies of bile mechanisms in vertebrates, identification of bisphenol‐A leaching from sterilized polycarbonate containers, high sensitivity TCDD analyses and other projects. Reflecting on my services for the mass spectrometry society, involvements with the co‐founding and 12 year chairing of the Asilomar Conference on Mass Spectrometry and founding of the Bay Area Mass Spectrometry regional MS discussion group, as part of my services for the mass spectrometry community, are presented in some detail. © 2016 Wiley Periodicals, Inc. Mass Spec Rev 36:520–542, 2017 相似文献
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Perspectives for mass spectrometry and functional proteomics 总被引:13,自引:0,他引:13
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The method of crosslinking combined with mass spectrometry is being gradually accepted as a technology enabling detailed structural information on proteins and protein complexes. Intrinsic challenges of the method, which have prevented its widespread use, are being progressively addressed by improvements in mass spectrometry instrumentation capabilities, by the development of new crosslinking reagents, and by the development of specialized software tools for processing of mass spectrometric crosslinking data. This review focuses on recent literature concerning the development of specialized crosslinking reagents and approaches for mass spectrometry‐based applications. Critical features of crosslinking reagents for optimum mass spectrometric performance, such as isotopic coding, cleavability, affinity groups, structure of the linkers, and reactive groups, are assessed. Requirements for the design of crosslinking reagents to make them well suited for mass spectrometric detection and analysis are summarized. © 2010 Wiley Periodicals, Inc. Mass Spec Rev 29:862–876, 2010 相似文献
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Progress in proteomics research has led to a demand for powerful analytical tools with high separation efficiency and sensitivity for confident identification and quantification of proteins, posttranslational modifications, and protein complexes expressed in cells and tissues. This demand has significantly increased interest in capillary electrophoresis‐mass spectrometry (CE‐MS) in the past few years. This review provides highlights of recent advances in CE‐MS for proteomics research, including a short introduction to top‐down mass spectrometry and native mass spectrometry (native MS), as well as a detailed overview of CE methods. Both the potential and limitations of these methods for the analysis of proteins and peptides in synthetic and biological samples and the challenges of CE methods are discussed, along with perspectives about the future direction of CE‐MS. @ 2019 Wiley Periodicals, Inc. Mass Spec Rev 00:1–16, 2019. 相似文献
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