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Elastomeric O-ring seals are used in a wide range of applications due to their excellent elasticity. However, like all polymers, elastomers degrade under the influence of e.g. time, temperature, oxygen, radiation and mechanical stress. Especially in applications where a replacement of seals after a certain time is hard or almost impossible, it is important to know the seal lifetime. Therefore, an extensive ageing programme with elastomers made of EPDM, HNBR and other materials was started with the aim of determining suitable methods for accelerated ageing and lifetime prediction.
In order to determine the lifetime of polymeric parts, the time-temperature superposition principle is commonly used to shift property changes obtained by accelerated ageing at higher temperatures to lower temperatures. If the shift factors yield a straight line in an Arrhenius diagram, a corresponding activation energy can be determined. However, we have found that the shift factors and thus the predicted lifetime depends on the test method that yielded the shifted data. For example, the shift factor between 125 °C and 150 °C ageing temperature was roughly the same (5/5/4.5 respectively) for hardness, density and maximum of loss factor tan measured on HNBR, but different for elongation at break (8) and compression set (2.2, excluding DLO-affected data). A possible explanation might be that while the different oxidation reactions proceed with a fixed activation energy, they have differing impact on the measured properties. For example, hardness is lowered by chain scission reactions, and increases by crosslinking reactions during ageing. As usually both chain scission and crosslinking reactions occur during ageing, the measured hardness increase reflects only the net effect of both reaction types. On the other hand, compression set is influenced additively by both reaction types: chain scission leads to an increase of the remaining deformation, as broken chains lose their recovery potential, and crosslinking reactions during ageing fix the compressed geometry, which also leads to less recovery. Thus, compression set reflects the total number of changes in the network and shows degradation effects much faster, which results in lower shift factors and lower activation energy. This phenomenon was observed for EPDM as well.
In order to verify our hypotheses and to gain further insights, temperature-dependent oxygen consumption measurements are currently being performed and results will be presented at the conference. The shift factors and activation energy determined by oxygen consumption measurements are expected to be close to the values for compression set.
Trapping in T24 steel weld joints – Effects on activation energy for hydrogen diffusion during TDA
(2017)
Failure cases in the past decade exhibited severe cracking in T24 welds and showed that generally hydrogen-assisted cracking (HAC) occurring up to 200°C cannot be excluded. A basic understanding is necessary on how hydrogen diffusion is influenced by the weld process. In this regard, both weld microstructures HAZ and weld metal have particular influence on hydrogen diffusion compared to the base material. In general, hydrogen diffusion at a certain temperature is described by diffusion coefficients representing an effective value of combined lattice diffusion and effects of reversible hydrogen traps. Those traps are typically precipitates, interstitials, grain boundaries and so on. A common approach to describe the trap character and its effect on diffusion is the determination of so-called activation energy. This can be done by respective thermal desorption analysis (TDA) with linear heating. In the present study, different T24 as-welded microstructures (BM, HAZ, WM) were investigated. For that purpose, electrochemically hydrogen charged specimens were analyzed by TDA with linear heating using a mass spectrometer for detection of ultra-low hydrogen amounts. The results showed that typically the as-welded HAZ had higher energy traps than the tempered base material. Nonetheless two important effects were ascertained: (1) it is strictly necessary to monitor the sample temperature due to its great impact on the hydrogen desorption peak temperature and (2) the real heating rate in the specimen vs. the applied heating rate has to be considered. Both influence the calculated activation energy, i.e. the assigned hydrogen trap character (moderate or strong trap), which changed up to a factor of two in terms of the calculated activation energy. This effect can be much more important compared to the microstructure effect itself. Hence, suitable experimental boundary conditions should be mandatory for the determination of hydrogen trap kinetics.
Mechanochemical reactions often result in 100% yields of single products, making purifying procedures obsolete. Mechanochemistry is also a sustainable and eco-friendly method. The ever increasing interest in this method is contrasted by a lack in mechanistic understanding of the mechanochemical reactivity and selectivity. Recent in situ investigations provided direct insight into formation pathways. However, the currently available theories do not predict temperature T as an influential factor. Here, we report the first determination of an apparent activation energy for a mechanochemical reaction. In a temperaturedependent in situ study the cocrystallisation of ibuprofen and nicotinamide was investigated as a model system. These experiments provide a pivotal step towards a comprehensive understanding of milling reaction mechanisms.
Pressure-assisted sintering (PAS) is an established procedure for the production of low-temperature cofired ceramics (LTCC) without lateral shrinkage and minimal shrinkage tolerances for automotive and high-frequency applications. To develop a feasible model for the prediction of densification during that process, master sintering curves (MSCs) for the commercial LTCC DP951 were generated from thermomechanical analysis (TMA) data in the pressure regime from 2 to 500 kPa. Strain mainly related to creep deformation of the LTCC was identified by evaluation of the strain rate and was discarded for the determination of MSC parameters. It was found that no creep occurred at any pressure up to a relative density of 0.9. Different pressure levels can be modeled with the same activation energy of 400 kJ/mol. Densification curves predicted by the model were in good agreement with experimental data. Based on MSCs, the pressure-assisted master sintering surface was compiled to illustrate the influence of pressure on densification. The results show that the MSC approach is a suitable method to feasibly predict the densification of LTCC during PAS.
Wear mechanisms, as adhesion, abrasion, fatigue and tribochemical wear, are complex in their physical and chemical nature. A theoretical description and prediction of wear are in most cases still far from reality. It is, therefore, important to use test rigs before a practical application of a given material combination under tribological loading.
On the other hand, model equations can be helpful for wear description, if a single wear mechanism is dominant.
Under oscillating and continuous sliding contact conditions, equations for wear calculation are presented to describe running-in and stationary wear behaviour of metals and ceramics. By using shear energy density, real area of contact, flash temperature, activation energy and numerical simulations with the method of movable cellular automata (MCA), wear data were calculated and compared to experimental laboratory results.