ANALYSIS OF C4 EXPLOSIVE RESIDUES ON POST BLAST HAIR SAMPLES

2012 ◽  
Vol 57 (1) ◽  
Author(s):  
UMI KALTHOM AHMAD ◽  
NOOR HIDAYAT ABU BAKAR ◽  
SHAIKH ABDUL ADZIZ SHAIKH ABDULLAH

The occurrence of crimes involving high explosives in Malaysia in recent years has warrant the need for the analysis of high explosives in post blast samples, particularly residues that could be found on hairs of victims. This study reports on the detection of post blast residues of C4 explosives on human head hairs. Prior to a simulated explosion, a bundle of hair (200 strands) was tightly bound to a metal hook at each point of several pre–determined distances from the bomb seat. Hair samples containing post blast residues were extracted by ultrasonication using acetonitrile. Two analytes of interest, cyclotrimethylenetrinitramine (RDX) and pentaerythritol tetranitrate (PETN) were successfully separated using gas chromatography with electron capture detector (GC–ECD) on an HP5–MS capillary column. It was found that the amount of explosive residues decreased with increasing distance from the point of blast. At the nearest specified distance of 2.5m, the amount of PETN residues deposited on hair was much less compared to that of RDX residues.

1984 ◽  
Vol 67 (2) ◽  
pp. 295-298
Author(s):  
Barry G Luke ◽  
Jeffrey C Richards ◽  
Ernest F Dawes

Abstract A redesigned fractionation tube has resulted in development of a new, commercial sweep co-distillation unit. It is compact, reliable, costefficient, and permits cleanup of pesticides in up to 10 fat samples simultaneously. Recovery of several organochlorine residues (HCB, ; BHC, lindane, heptachlor epoxide, dieldrin, p,p'-DDE, p,p'-DDD, p,p'-DDT) at ppm and ppb levels in meat (beef) fat are 83-105%, with coefficients of variation between 4 and 6%. Cleaned up extracts are quantitated by gas chromatography using an electron capture detector with a vitreous silica capillary column containing a medium polarity bonded phase.


1971 ◽  
Vol 54 (3) ◽  
pp. 711-712
Author(s):  
Martha Fuzesi

Abstract A gas chromatographic method is described for the quantitative determination of N-butyl-N-ethyl-α,α,α-trifluoro-2,6-dinitro-p-tolindine and α,α,α-trifluoro-2,6-dinitro-N,N-dipropyI-p-toluidine herbicides in formulations. The sample is extracted with benzene, and equal amounts of sample and reference solution in the same concentration range are analyzed by gas chromatography, using an electron capture detector and an SE-30/Diatoport S column. The method has been applied successfully to laboratory-prepared and commercial samples.


2012 ◽  
Vol 134 (4) ◽  
pp. 2424-2429 ◽  
Author(s):  
Shengbing Yu ◽  
Binghui Zhu ◽  
Fen Lv ◽  
Shaoxiao Li ◽  
Weixiong Huang

1991 ◽  
Vol 74 (5) ◽  
pp. 830-835 ◽  
Author(s):  
Dalia M Gilvydis ◽  
Stephen M Walters

Abstract An interlaboratory study of the determination of captan, folpet, and captafol in tomatoes, cucumbers, and apples was conducted by 4 laboratories using wide-bore capillary column gas chromatography with electron capture detection. The 3 fungicides were determined using the Luke et al. multlresidue method modified to Include additional solvent elutlon in the optional Florisll column cleanup step used with this method. The crops were fortified with each fungicide at 3 levels per crop. Mean recoveries ranged from 86.2% for a 25.1 ppm level of captan in apples to 115.4% for a 0.288 ppm level of captafol In apples. Interlaboratory coefficients of variation ranged from 3.4% (24.7 ppm folpet) to 9.7% (0.243 ppm captafol) for tomatoes; from 2.8% (2.0 ppm captafol) to 8.2% (24.8 ppm captan) for cucumbers; and from 1.5% (0.234 ppm folpet) to 22.1% (0.266 ppm captafol) for apples.


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