Polyolefin geosynthetics are susceptible to oxidative degradation, which in turn leads to diminished mechanical properties in geotechnical constructions. When using these materials, it is extremely important to determine their durability over time in particularly aggressive conditions. In order to prolong the life of a geosynthetic material, antioxidants are added during the manufacturing process. The function of antioxidants is to prevent polymer oxidation reaction in time. As the antioxidant content is depleted, the polymer becomes less protected towards oxidative attacks. This article describes the aging process of uniaxial (high density polyethylene) HDPE geogrids under the influence of chemical and environmental factors. Evaluations of accelerated aging test of the uniaxial HDPE geogrids were incubated in simulated landfill conditions for a period of 12 months. Three temperatures (25 °C, 45 °C, and 75 °C) were selected for carrying out the aging experiments in aqueous solutions mimicking landfill conditions. The changes observed by differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR) and melt flow index (MFI) correlate with the mechanical properties of the aged geogrid. No significant changes in the FTIR and MFI were observed over the 12 months of accelerated aging tests at none of the three different temperatures. The oxidation induction time (OIT) test showed no antioxidant remaining in the geogrid following eight months of aging test at 75 °C. No significant changes in the influence of accelerated aging tests on the average relative elongation at 25 °C and 45 °C of the tested material were observed. Accelerated aging tests at 75 °C showed that the mean elongation of 12.12% for the sample not subjected to accelerated aging tests (new sample) increased to 19.32% (after 12 months of incubation).

The article presents a technique of differential ion mobility spectrometry (DMS) applicable to the detection and identification of volatile organic compounds (VOCs) from such categories as n-alkanes, alcohols, acetate esters, ketones, botulinum toxin, BTX, and fluoro- and chloro-organic compounds. A possibility of mixture identification using only the DMS spectrometer is analyzed, and several examples are published for the first time. An analysis of different compounds and their mechanisms of fragmentation, influence on effective ion temperature, and high electric field intensity is discussed.