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Examination of Firearms Review: 2007 to 2010 - Interpol

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sensitivity <strong>of</strong> the method is important. In diesel fuel characterization the Supersonic<br />

GC-MS achieved the ppb -level (ng/ml). Biodiesel samples were also studied but the<br />

analysis was made without pre-treating the samples. The molecular ions <strong>of</strong> the<br />

samples were discovered. The method was found adaptable <strong>to</strong> use in forensic<br />

work. 63 Another type <strong>of</strong> separation capacity is considered when GC-MS is used in<br />

analysing alkylcyclohexanes. The purpose <strong>of</strong> the method was <strong>to</strong> determine whether<br />

the residues found in the fire debris were kerosene, gas oil or plastic based. 64<br />

Another suggested method for the characterization <strong>of</strong> gasoline samples is multidimensional<br />

GC-fourier transform ion cyclotron resonance MS analysis (GC-FT-ICR-<br />

MS). The author <strong>of</strong> the study refers <strong>to</strong> fingerprinting crude oils and refined petroleum<br />

products. Therefore the use <strong>of</strong> chemical ionization, with pro<strong>to</strong>nated reagent ions, can<br />

be used <strong>to</strong> identify the presence <strong>of</strong> co-eluting isomers in gasoline samples. When<br />

necessary, the method includes dimensions that can be added <strong>to</strong> the analysis in<br />

order <strong>to</strong> achieve greater accuracy. 65<br />

A different kind <strong>of</strong> detec<strong>to</strong>r for forensic work, ion mobility spectrometry (IMS), has<br />

been evaluated and developed. An article and a review written about the method, its<br />

his<strong>to</strong>ry, ion source development and applications serve <strong>to</strong> deepen the know-how <strong>of</strong> a<br />

fire analyst. The method is expected <strong>to</strong> play a significant role in ignitable liquid and<br />

66, 67<br />

arson investigations.<br />

In addition <strong>to</strong> the study mentioned in the previous section, there have been two novel<br />

studies made; firstly, an application <strong>of</strong> gas chroma<strong>to</strong>graphy differential mobility<br />

spectrometry (GC-DMS) with two-way classification <strong>of</strong> ignitable liquids in fire debris.<br />

The GC-DMS provides unique pr<strong>of</strong>iles for different ignitable liquids and, combined<br />

with the fuzzy rule building expert system (FuRES) on two-way data objects, the<br />

system was successful in forensic analysis <strong>of</strong> fire debris. Also the method seemed<br />

promising for onsite detection for arson investigation. 68 Secondly, the same writer<br />

has published a comparison <strong>of</strong> different detection methods in order <strong>to</strong> value their<br />

performances in ignitable liquid classification by using gas chroma<strong>to</strong>graphy coupled<br />

with either differential mobility spectrometry or mass spectrometry, GC-DMS and GC-<br />

MS respectively. The comparison <strong>of</strong> the methods was made with projected difference<br />

resolution (PDR) and the results were furthermore verified by FuRES. One-way<br />

datasets were determined in order <strong>to</strong> calculate minimum resolution values. The<br />

results were that MS data achieved higher resolution, but DMS gained more<br />

informative data. The two way (2D-GC) datasets in neat samples demonstrated that<br />

GC-MS would have had smaller prediction errors than DMS in classifying the<br />

ignitable liquids. No statistic difference occurred between the two methods<br />

considering the high resolution values <strong>of</strong> neat and spiked samples, yet with burned<br />

samples a smaller prediction error was obtained with GC-MS. 69<br />

Detection <strong>of</strong> gasoline and paint thinner directly from common household material has<br />

been studied. The analysis method is a direct analysis <strong>of</strong> real time mass<br />

spectrometry (DART). The method does not need sample pre-treatment. Samples<br />

are introduced at atmospheric pressure and placed in<strong>to</strong> a stream <strong>of</strong> exited gas, from<br />

which analytes are desorbed and ionized. The method has been demonstrated <strong>to</strong> be<br />

sensitive and chemical fingerprinting was obtained when samples were analysed<br />

within 1-24 hours after being spiked. Further studies considering matrices and related<br />

effects for detection are proposed. 70 DART is also mentioned in a review article<br />

430

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