电解槽操作无气瓶气相色谱fid

Gad Frishman, Nitzan Tzanani, Aviv Amirav
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引用次数: 6

摘要

一种新的气相色谱系统,基于使用水电解槽作为其唯一的气体来源,设计,建造和测试。电解动力火焰电离检测器(EFID)作为气相色谱检测器,用于广泛的挥发性有机化合物的敏感,碳选择性检测。电解槽操作气相色谱-EFID的概念是基于使用电解槽产生的氧气和氢气混合物在吹扫和捕集取样系统中进行样品解吸和清扫,作为分析柱载气和唯一需要的EFID可燃气体混合物。发现,正如以前发现的那样,具有二甲基聚硅氧烷吸附膜的标准色谱柱可以在高达200°C的氧气下操作。采用基于苯乙烯-二乙烯苯的PoraBOND多孔层开管柱进行气相色谱分离,发现该系统可以在电解产生的氢气和氧气混合物中高达140℃的温度下工作。因此,使用水电解槽可以创建无气瓶的GC-FID系统,具有更强的可运输性和易用性,并且操作成本更低。无气瓶系统的操作证明了快速色谱分离丙酮,乙醇,苯,甲苯和二甲苯(在1分钟的总分析时间内),估计检测限低于1 ppb。证明了人类呼出气体分析在工业卫生和医学诊断应用中的能力。显示了空气中总烃含量分析的附加能力,并讨论了所需的小修改。©2001 John Wiley &儿子,Inc。化学工程学报(英文版),2001
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrolyzer-operated gas-cylinder-free GC-FID

A new gas chromatography system, based on the use of a water electrolyzer as its only source of gases, was designed, built, and tested. An electrolyzer-powered flame ionization detector (EFID) served as the GC detector for the sensitive, carbon-selective detection of a broad range of volatile organic compounds. The concept of electrolyzer-operated GC-EFID is based on the use of the electrolyzer-produced oxygen and hydrogen gas mixture for sample desorption and sweeping in a purge-and-trap sampling system, as the analytical column carrier gas and as the only required EFID combustible gas mixture. It was found, as it has been found previously, that standard columns with dimethyl polysiloxane adsorption film could be operated with oxygen up to 200 °C. A styrene-divinylbenzene–based PoraBOND porous-layer open tubular column was used for the GC separation, and it was found that the system could be operated up to 140 °C with the electrolyzer-produced hydrogen and oxygen gas mixture. Thus, the use of a water electrolyzer enabled the creation of a gas-cylinder-free GC-FID system with enhanced transportability and ease of use and with lower cost of operation. The gas-cylinder-free system operation was demonstrated with fast chromatography separation (under 1-min total analysis time) of acetone, ethanol, benzene, toluene, and xylene with an estimated detection limit below 1 ppb. The capability of exhaled human breath analysis for industrial hygiene and medical diagnostic applications is demonstrated. An additional capability of total hydrocarbon content in air analysis is shown and the required minor modifications are discussed. © 2001 John Wiley & Sons, Inc. Field Analyt Chem Technol 5: 107–115, 2001

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