Cracking occurred within the plastic jacket (injection molded from an impact-modified, 15% glass-fiber-reinforced PET resin.) of several assemblies used in a transportation application during an engineering testing regimen which involved cyclic thermal shock (exposing the parts to alternating temperatures of -40 and 180 deg C (-40 and 360 deg F)). Prior to molding, the resin had reportedly been dried at 135 deg C (275 deg F). The drying process usually lasted 6 h, but occasionally, the material was dried overnight. Comparison investigation (visual inspection, 20x SEM views, micro-FTIR, and analysis using DSC and TGA) with non-failed parts supported the conclusion that that the failure was via brittle fracture associated with the exertion of stresses that exceeded the strength of the resin as-molded caused by the disparity in the CTEs of the PET jacket and the mating steel sleeve. The drying process had exposed the resin to relatively high temperatures, which caused substantial molecular degradation, thus limiting the part's ability to withstand the stresses. The drying temperature was found to be significantly higher than the recommendation for the PET resin, and the testing itself exposed the parts to temperatures above the recognized limits for PET.

A production lot of plastic wire clips was failing after limited service. The failures were characterized by excessive relaxation of the clips, such that the corresponding wires were no longer adequately secured in the parts. No catastrophic failures had been encountered. Parts representing an older lot, which exhibited satisfactory performance properties, were also available for reference purposes. The clips were specified to be injection molded from an impact-modified grade of nylon 6/6. However, the part drawing did not indicate a specific resin. Investigation included visual inspection, micro-FTIR in the ATR mode, and analysis using DSC. The spectrum representing the reference parts showed a relatively higher level of a hydrocarbon-based impact modifier, while the results obtained on the failed parts showed the presence of an acrylic-based modifier. Also, the reference clip thermogram showed a melting transition attributed to a hydrocarbon-based impact modifier. The conclusion was that the control and failed clips had been produced from two distinctly different resins. It appeared that the material used to produce the failed clips had different viscoelastic properties, which produced a greater predisposition for stress relaxation.

The handle from a consumer product exhibited an apparent surface defect. The handle had been injection molded from a medium viscosity grade ABS resin. The anomalous appearance was objectionable to the assembler of the final product and resulted in a production lot being placed on quality-control hold. Investigation included visual inspection, 24x micrographs, and FTIR in the reflectance mode. The spectrum obtained on the included material was characteristic of polybutadiene, the rubber-modifying agent present in ABS. This supported the conclusion that the inclusion's most likely source was an undispersed gel particle formed during the production of the molding resin.

Components of a latch assembly used in a consumer safety restraint exhibited a relatively high failure rate. The failures were occurring after installation but prior to actual field use when failure could result in severe injury. Cracking occurred within retaining tabs used to secure a metal slide on an older design, whereas newer components showed no signs of failure. The latch assembly components were injection molded from an unfilled commercial grade of a polyacetal copolymer. Investigation of failed parts (including visual inspection, a specially designed proof load test, 59x SEM images, micro-FTIR in the ATR mode, and DSC/TGA/MFR analysis) showed no evidence of contamination or degradation from the molding process. The conclusion was that the parts failed via brittle fracture associated with stress overload. The stress overload was accompanied by severe apparent embrittlement resulting from a relatively high strain rate event and/or significant stress concentration. A relatively sharp corner formed by a retaining tab on the older design was shown to be a primary cause of the failures.

A set of plastic grips from an electric consumer product failed while in service. The grips had been injection molded from a general-purpose grade of ABS resin. The parts had cracked while in use after apparent embrittlement of the material. Investigation (visual inspection, SEM imaging, and micro-FTIR in the ATR mode) showed that the spectrum representing the grip surface contained absorption bands associated with ABS as well as additional bands of significant intensity. A spectral subtraction removed the bands associated with the ABS resin resulting in a very good match with glyceride derivatives of fats and oils. This supported the conclusion that the grips failed via brittle fracture associated with severe chemical attack of the ABS resin. A significant level of glyceride derivatives of fatty acids, known to degrade ABS resins, was found on the part surface.

A plastic bracket exhibited relatively brittle material properties, which ultimately led to catastrophic failure. The part had been injection molded from a medium-viscosity polycarbonate resin and had been in service for a short duration prior to the failure. Investigation (visual inspection and analysis using micro-FTIR in the ATR mode) revealed the spectrum showed changes in the relative intensities of several bands, as compared to the results representing the base material. A spectral subtraction was performed, and the results produced a good match with diphenyl carbonate, which is a common breakdown product produced during the decomposition of polycarbonate. The conclusion was that the most likely cause of the molecular degradation was improper drying and/or exposure to excessive heat during the injection molding process that in turn caused the material degradation.