化学
电喷雾电离
电离
电喷雾
解吸电喷雾电离
质谱法
离子源
大气压力
化学电离
环境电离
大气压化学电离
分析化学(期刊)
直接电子电离液相色谱-质谱联用界面
电子电离
萃取电喷雾电离
透视图(图形)
流量(数学)
光离子化
飞镖离子源
离子
色谱法
体积流量
标识
DOI:10.1021/jasms.5c00375
摘要
This Account is a personal perspective on the development of the current atmospheric pressure ionization (API) LC/MS techniques. These include atmospheric pressure chemical ionization (APCI), which appeared first, followed by electrospray ionization. Early commercial LC/MS interfaces began to appear in the late 1970s coupled with either electron ionization (EI) or chemical ionization (CI) ion sources, which operated under vacuum. There was an understandable challenge in successfully coupling the HPLC effluent liquid introduction into a vacuum system. The analytical success for the early LC/MS interfaces was slow until John Fenn published his results on the nano flow infusion electrospray analysis with an atmospheric pressure ionization (API) mass spectrometer. Our laboratory was excited about Fenn's report, but we were concerned that the current HPLC techniques operated at mobile phase flow rates much too high for Fenn's electrospray. We commenced studies to increase the ability of electrospray to operate at higher liquid flows by implementing a high flow of nitrogen gas coaxially with the electrospray emitter. This became pneumatically assisted electrospray, which we later called Ion Spray. This technique eventually became commercially available from each mass spectrometer vendor and today is called "electrospray" even though it is actually "Ion Spray".
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