𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Using the tools of chromatography, mass spectrometry, and automated data processing in the detection of arson

✍ Scribed by Bertsch, Wolfgang ;Zhang, Q. W. ;Holzer, Günther


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
901 KB
Volume
13
Category
Article
ISSN
0935-6304

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The analysis of residual accelerants in fire debris is commonly carried out by a three‐step procedure: sample preparation; separation and detection; and data interpretation. Each of these steps can be optimized individually but successful analysis requires that they are compatible with each other. The isolation of residual accelerant from fire debris requires that several methods are used to cover the range of fueis that are commonly used by arsonists. Since almost all incendiary fires are set with petroleum based fuels such as gasoline or heating oil, analysis is targeted toward hydrocarbons. Capillary column gas chromatography on apolar phases is now the overwhelmingly predominant method of separation. Data interpretation is commonly carried out by visual comparison of chromatograms.

Fire debris analysis presents some unique challenges that are not often encountered in other fields. The analyte may be present at only trace levels and pyrolysis products from building materials or furnishings may dominate chromatographic patterns. Synthetic polymers may act as precursors to hydrocarbons that compete with substances typically found in petroleum based fuels. Exposure to heat and other environmental factors may also generate severe distortions in the chromatographic profiles of accelerants.

Unfortunately, there is no simple solution to these problems. Methods are available to reduce some of the chemical noise introduced by interferences and thus enhance the recognizability of the target substances. Mass spectrometry, in combination with a modern data system, is the most effective approach to filter out unwanted substances. The interpretation of the analytical results is aided by scaling, side‐by‐side comparison, or stacking of chromatograms. An additional advantage of such computerized systems is the possibility of complete automation of the analysis.

In this communication, we look at the interplay of chromatographic resolution, noise reduction by mass spectrometry, and automated data evaluation. Examples from model experiments and from simulated arson samples are presented.


📜 SIMILAR VOLUMES


The resolution of mixtures using data fr
✍ J.Martin Phalp; Alan W. Payne; Willem Windig 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 852 KB

This paper describes the application of self-modeling mixture analysis to automated mass spectral data analysis. The particular method chosen here is SIMPLISMA (Simple to use Interactive Self-Modelling Mixture Analysis). This method requires extensive user-interaction and as such is not applicable t

Comparison of two methods of detection,
✍ B.Edwin Blaisdell; S.C. Gates; F.E. Martin; C.C. Sweeley 📂 Article 📅 1980 🏛 Elsevier Science 🌐 English ⚖ 769 KB

A comparison is made of two different methods, LlANAL and kISSMET, for the analysis of a g.c.-ms. data matrix for the purpose of detecting and determining the metabolic profiles of the substances present. The parameters of the methods and the profiles determined on two different data matrices are co

Combination of liquid chromatography/tan
✍ Christof Van Poucke; Mario Van De Velde; Carlos Van Peteghem 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 152 KB

## Abstract For the detection of anabolic steroid residues in bovine urine, a highly sensitive liquid chromatographic/electrospray ionization tandem mass spectrometric (LC/ESI‐MS/MS) method was developed using both positive and negative ionization. For four compounds the ESI mode was not sensitive