- Forensic chemistry
Forensic chemistry is the application of
chemistryto law enforcement or the failure of products or processes. Many different analytical methods may be used to reveal what chemical changes occurred during an incident, and so help reconstruct the sequence of events.
One useful method is the gas chromatograph-mass spectrometer (GCMS), which is actually two instruments that are attached. The
gas chromatographis essentially a very hot oven holding a hollow coiled column. A drug sample is diluted in a solvent(e.g.: chloroform, methanol) and is injected into this column, the solventwill evaporate very quickly leaving the drug to travel through the column. Different substances are retained in the column for different amounts of time. The retention time, as compared to a known standard sample using the same method(same column length/polarity, same flow rate, same temperature program), can help to provide a positive identification for the presence of a compound of interest. The column eluentis then fed into a mass spectrometer. A mass spectrometerbombards the eluant with electrons, causing it to fragment into ions. These ions are separated by their mass, commonly with the use of a quadrupole mass analyzeror quadrupole ion trap, and detected by an electron multiplier. This provides a fragmentation pattern, which functions as a sort of fingerprint for each compound, and is compared to a reference sample.
Another instrument used to identify controlled substances is Fourier Transform infrared spectrophotometer (
FTIR). The FTIRrecords the bending and stretching of molecular bonds that are exposed to infrared light. The molecular bonds of all compounds react differently and create unique patterns upon exposure to a beam of infrared light. The unique pattern created is known as the fingerprint for that drug. As with the GCMS the results of the FTIRare compared to a known drug sample, thus producing a definitive identification. Spectroscopy can also help to identify materials used in failed products, especially polymers, additives and fillers. Samples can be taken by dissolution, or by cutting a thin slice using a microtomefrom the specimen under examination. Surfaces can be examined using Attenuated total reflectancespectroscopy, and the method has also been adapted to the optical microscopewith infra-red microspectroscopy.
Forensic chemists usually perform their analytical work in a sterile laboratory decreasing the risk of sample contamination. In order to prevent tampering, forensic chemists must keep track of a chain of custody for each sample. A chain of custody is a document which stays with the evidence at all times. Among other information, contains signatures and identification of all the people involved in transport, storage and analysis of the evidence.
This makes it much more difficult for intentional tampering to occur, it also acts as a detailed record of the location of the evidence at all times for record keeping purposes. It increases the reliability of a forensic chemist's work and increases the strength of the evidence in court.
A distinction is made between destructive and non-destructive analytical methods. Destructive methods involve taking a sample from the object of interest, and so injures the object. Most spectroscopic techniques fall into this category. By contrast, a non-destructive method conserves the integrity of the object, and is generally preferred by forensic examiners. Optical microsocopy cannot injure the sample, so fall into this class.
Polymers for example, can be attacked by aggressive chemicals, and if under load, then cracks will grow by the mechanism of stress corrosion cracking. Perhaps the oldest known example is the ozonecracking of rubbers, where traces of ozone in the atmosphere attack double bondsin the chains of the materials. Elastomers with double bonds in their chains include natural rubber, nitrile rubberand styrene-butadienerubber. They are all highly susceptible to ozone attack, and can cause problems like car fires (from rubber fuel lines) and tyre blow-outs. Nowadays, anti-ozonants are widely added to these polymers, so the incidence of cracking has dropped. However, not all safety-critical rubber products are protected, and since only ppbof ozone will start attack, failures are still occurring.
Another highly reactive gas is
chlorine, which will attack susceptible polymers such as acetal resinand polybutylenepipework. There have been many examples of such pipes and acetal fittings failing in properties in the USA as a result of chlorine-induced cracking. Essentially the gas attacks sensitive parts of the chain molecules (especially secondary, tertiary or allylic carbon atoms), oxidising the chains and ultimately causing chain cleavage. The root cause is traces of chlorine in the water supply, added for its anti-bacterial action, attack occurring even at parts per milliontraces of the dissolved gas.
Most step-growth polymers can suffer
hydrolysisin the presence of water, often a reaction catalysed by acidor alkali. Nylonfor example, will degrade and crack rapidly if exposed to strong acids, a phenomenon well known to those who accidentally spill acid onto their shirts or tights. Polycarbonateis susceptible to alkali hydrolysis, the reaction simply depolymerising the material. Polyestersare prone to degrade when treated with srong acids, and in all these cases, care must be taken to dry the raw materials for processing at high temperatures to prevent the problem occurring.
Many polymers are also attacked by
UV radiationat vulnerable points in their chain structures. Thus polypropylenesuffers severe cracking in sunlightunless anti-oxidants are added. The point of attack occurs at the tertiary carbon atom present in every repeat unit, causing oxidation and finally chain breakage.
Environmental stress cracking
Forensic polymer engineering
Stress corrosion cracking
*Lewis,P R, Gagg, R and Reynolds, K, "Forensic Materials Engineering: Case Studies" CRC Press (2004).
*Lewis, P R and Hainsworth S, "Fuel Line Failure from stress corrosion cracking", Engineering Failure Analysis,13 (2006) 946-962.
* Ezrin, Meyer, "Plastics Failure Guide: Cause and Prevention", Hanser-SPE (1996).
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