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动态顶空生成和三丙酮三过氧化物蒸气的定量分析。

Dynamic headspace generation and quantitation of triacetone triperoxide vapor.

机构信息

Chemistry Division, U.S. Naval Research Laboratory, Washington, DC 20375, USA.

Nova Research, Inc., Alexandria, VA 22308, USA.

出版信息

J Chromatogr A. 2014 Feb 28;1331:38-43. doi: 10.1016/j.chroma.2014.01.045. Epub 2014 Jan 24.

DOI:10.1016/j.chroma.2014.01.045
PMID:24508355
Abstract

Two methods for quantitation of triacetone triperoxide (TATP) vapor using a programmable temperature vaporization (PTV) inlet coupled to a gas chromatography/mass spectrometer (GC/MS) have been demonstrated. The dynamic headspace of bulk TATP was mixed with clean humid air to produce a TATP vapor stream. Sampling via a heated transfer line to a PTV inlet with a Tenax-TA™ filled liner allowed for direct injection of the vapor stream to a GC/MS for vapor quantitation. TATP was extracted from the vapor stream and subsequently desorbed from the PTV liner for splitless injection on the GC column. Calibration curves were prepared using solution standards with a standard split/splitless GC inlet for quantitation of the TATP vapor. Alternatively, vapor was sampled onto a Tenax-TA™ sample tube and placed into a thermal desorption system. In this instance, vapor was desorbed from the tube and subsequently trapped on a liquid nitrogen cooled PTV inlet. Calibration curves for this method were prepared from direct liquid injection of standards onto samples tube with the caveat that a vacuum is applied to the tube during deposition to ensure that the volatile TATP penetrates into the tube. Vapor concentration measurements, as determined by either GC/MS analysis or mass gravimetry of the bulk TATP, were statistically indistinguishable. Different approaches to broaden the TATP vapor dynamic range, including diluent air flow, sample chamber temperature, sample vial orifice size, and sample size are discussed. Vapor concentrations between 50 and 5400ngL(-1) are reported, with stable vapor generation observed for as long as 60 consecutive hours.

摘要

两种使用程序升温汽化(PTV)进样口与气相色谱/质谱联用仪(GC/MS)定量三乙酰基过氧化物(TATP)蒸气的方法已经得到了证明。将大块 TATP 的动态顶空与清洁的湿空气混合,产生 TATP 蒸气流。通过加热传输线将蒸气流采样到填充 Tenax-TA™的 PTV 进样口,可直接将蒸气流注入 GC/MS 进行蒸气定量。TATP 从蒸气流中提取出来,随后从 PTV 衬管中解吸出来,用于 GC 柱上的不分流注射。通过使用溶液标准品并带有标准分流/不分流 GC 进样口来制备校准曲线,可对 TATP 蒸气进行定量。或者,蒸气被采样到 Tenax-TA™样品管中,并放入热解吸系统中。在这种情况下,蒸气从管中解吸出来,并随后被液氮冷却的 PTV 进样口捕获。从标准品直接注入样品管中制备了该方法的校准曲线,但需要注意的是,在沉积过程中对管施加真空,以确保挥发性 TATP 渗透到管中。通过 GC/MS 分析或大块 TATP 的质量 gravimetry 确定的蒸气浓度测量值在统计学上是不可区分的。讨论了扩大 TATP 蒸气动态范围的不同方法,包括稀释空气流量、样品室温度、样品小瓶孔口尺寸和样品量。报告了 50 至 5400ngL(-1)之间的蒸气浓度,并且观察到长达 60 个连续小时的稳定蒸气生成。

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