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22-AUGUST-2008 06:13:22 - Forensic polymer engineering This article or section includes a list of references or external links, but its sources remain unclear because it lacks in-text citations. You can improve this article by introducing more precise citations where appropriate. The study of failure in polymeric products is called forensic polymer engineering. The topic includes the fracture of plastic products, or any other reason why such a product fails in service, or fails to meet its specification. The subject focuses on the material evidence from crime or accident scenes, seeking defects in those materials which might explain why an accident occurred, or the source of a specific material to identify a criminal. Many analytical methods used for polymer identification may be used in investigations, the exact set being determined by the nature of the polymer in question, be it thermoset, thermoplastic, elastomeric or composite in nature. One aspect is the analysis of trace evidence such as skid marks on exposed surfaces, where contact between dissimilar materials leaves material traces of one left on the other. Provided the traces can be analyzed successfully, then an accident or crime can often be reconstructed. Contents 1 Methods of analysis 2 Fracture 3 Examples 3.1 Ozone cracking 3.2 Chlorine-induced cracking 3.3 Hydrolysis 3.4 UV degradation 4 See also 5 References 6 External Links Methods of analysis IR spectrum showing carbonyl absorption due to oxidative degradation of polypropylene IR spectrum showing carbonyl absorption due to oxidative degradation of polypropylene Thermoplastics can be analysed using infra-red spectroscopy, UV spectroscopy, as NMR and ESEM. Failed samples can either be dissolved in a suitable solvent and examined directly UV, IR and NMR spectroscopy or as a thin film cast from solvent or cut using microtomy from the solid product. Infra-red spectrosocpy is especially useful for assessing oxidation of polymers, such as the polymer degradation caused by faulty injection moulding. The spectrum shows the characteristic carbonyl group produced by oxidation of polypropylene, which made the product brittle. It was a critical part of a crutch, and when it failed, the user fell and injured herself very seriously. The spectrum was obtained from a thin film cast from a solution of a sample of the plastic taken from the failed forearm crutch. Microtomy is preferable since there are no complications from solvent absorption, and the integrity of the sample is partly preserved. Thermosets, composites and elastomers can often only be examined using microtomy owing to the insoluble nature of these materials. Fracture Fractured products can be examined using fractography, an especially useful method for all broken components using macrophotography and optical microscopy. Although polymers usually possess quite different properties to metals, ceramics and glasses, they are just as susceptible to failure from mechanical overload, fatigue and stress corrosion cracking if products are poorly designed or manufactured. Scanning electron microscopy or ESEM is especially useful for examining fracture surfaces and can also provide elemental analysis of viewed parts of the sample being investigated. It is effectively a technique of microanalysis and valuable for examination of trace evidence. On the other hand, colour rendition is absent in ESEM, and there is no information provided about the way in which those elements are bonded to one another. Specimens will be exposed to a partial vacuum, so any volatiles may be removed, and surfaces may be contaminated by substances used to attach the sample to the mount. Examples Many polymers are attacked by specific chemicals in the environment, and serious problems can arise, including road accidents and personal injury. Polymer degradation leads to sample embrittlement, and fracture under low applied loads. Ozone cracking Ozone cracking in Natural rubber tubing Ozone cracking in Natural rubber tubing 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 ozone cracking of rubbers, where traces of ozone in the atmosphere attack double bonds in the chains of the materials. Elastomers with double bonds in their chains include natural rubber, nitrile rubber and styrene-butadiene rubber. They are all highly susceptible to ozone attack, and can cause problems like vehicle 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 ppb of ozone will start attack, failures are still occurring. Chlorine-induced cracking chlorine attack of acetal resin plumbing joint chlorine attack of acetal resin plumbing joint Another highly reactive gas is chlorine, which will attack susceptible polymers such as acetal resin and polybutylene pipework. 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 million traces of the dissolved gas. The chlorine attacks weak parts of a product, and in the case of an acetal resin junction in a water supply system, it was the thread roots which were attacked first, causing a brittle crack to grow. The discolouration on the fracture surface was caused by deposition of carbonates from the hard water supply, so the joint had been in a critical state for many months. When it finally failed, it did so at the worst possible time, at the weekend when no-one was around to sort the problem. The leak flooded computer labs below, and caused substantial damage. Hydrolysis Most step-growth polymers can suffer hydrolysis in the presence of water, often a reaction catalysed by acid or alkali. Nylon for example, will degrade and crack rapidly if exposed to strong acids, a phenomenon well known to ladies who accidentally spill acid onto their tights. Failed fuel pipe at right from road traffic accident Failed fuel pipe at right from road traffic accident The broken fuel pipe shown at right caused a serious accident when diesel fuel poured out from a van onto the road. A following car skidded and the driver was seriously injured when she collided with an oncoming lorry. Scanning electron microscopy or SEM showed that the nylon connector had fractured by stress corrosion cracking due to a small leak of battery acid. Nylon is susceptible to hydrolysis in contact with sulfuric acid, and only a small leak of acid would have sufficed to start a brittle crack in the injection moulded connector by a mechanism known as stress corrosion cracking, or SCC. Close-up of broken fuel pipe Close-up of broken fuel pipe The crack took about 7 days to grow across the diameter of the tube, hence the van driver should have seen the leak well before the crack grew to a critical size. He did not, therefore resulting in the accident. The fracture surface showed a mainly brittle surface with striations indicating progressive growth of the crack across the diameter of the pipe. Once the crack had penetrated the inner bore, fuel started leaking onto the road. Diesel is especially hazardous on road surfaces because it forms a thin oily film which cannot be seen easily by drivers. It is akin to black ice in lubricity, so skids are common when diesel leaks occur. The insurers of the van driver admitted liability and the injured driver was compensated. Polycarbonate is susceptible to alkali hydrolysis, the reaction simply depolymerising the material. Polyesters are 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. UV degradation IR spectrum showing carbonyl absorption due to UV degradation of polyethylene IR spectrum showing carbonyl absorption due to UV degradation of polyethylene Many polymers are also attacked by UV radiation at vulnerable points in their chain structures. Thus polypropylene suffers severe cracking in sunlight unless 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. Polyethylene is also susceptible to UV degradation, especially those variants which are branched polymers such as LDPE. The branch points are tertiary carbon atoms, so polymer degradation starts there and results in chain cleavage, and embrittlement. In the example shown at left, carbonyl groups were easily detected by IR spectroscopy from a cast thin film. The product was a road cone which had cracked in service, and many similar cones also failed because a anti-UV additive had not been used. See also Applied spectroscopy Catastrophic failure Circumstantial evidence Environmental stress cracking Forensic chemistry Forensic electrical engineering Forensic evidence Forensic photography Forensic engineering Forensic materials engineering Forensic science Fractography Ozone cracking Polymer degradation Skid mark Stress corrosion cracking Trace evidence UV degradation References Peter R Lewis and Sarah Hainsworth, Fuel Line Failure from stress corrosion cracking, Engineering Failure Analysis,13 2006 946-962. Lewis, Peter Rhys, Reynolds, K, Gagg, C, Forensic Materials Engineering: Case studies, CRC Press 2004. Wright, D.C., Environmental Stress Cracking of Plastics RAPRA 2001. Ezrin, Meyer, Plastics Failure Guide: Cause and Prevention, Hanser-SPE 1996. External Links Museum of failed products New Forensic course The journal Engineering Failure Analysis Forensic science and engineering Retrieved from http://en..org/wiki/Forensic_polymer_engineering Categories: Forensics | Materials science | PolymersHidden category: Articles lacking in-text citations Views Article Discussion this page History Personal tools Log in / create account Navigation Main page Contents Featured content Current events Random article Search Go Search Interaction Community portal Recent changes Contact Donate to Help Toolbox What links here Related changes Upload file Special pages Printable version Permanent link Cite this page This page was last modified on 23 May 2008, at 04:49. of the GNU Free Documentation License. ® , Inc., a U.S.
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