Numerous assays were developed to measure the antioxidant activity, but each has limitations and the results obtained by different methods are not always comparable. Popular examples are the DPPH and ABTS assay. Our aim was to study similarities and differences of these two assay regarding the measured antioxidant potentials of 24 phenolic compounds using the same measurement and evaluation methods. This should allow conclusions to be drawn as to whether one of the assays is more suitable for measuring specific subgroups like phenolic acids, flavonols, flavanones, dihydrochalcones or flavanols. The assays showed common trends for the mean values of most of the subgroups. Some dihydrochalcones and flavanones did not react with the DPPH radical in contrast to the ABTS radical, leading to significant differences. Therefore, to determine the antioxidant potential of dihydrochalcone or flavanone-rich extracts, the ABTS assay should be preferred. We found that the results of the flavonoids in the DPPH assay were dependent on the Bors criteria, whereas the structure–activity relationship in the ABTS assay was not clear. For the phenolic acids, the results in the ABTS assay were only high for pyrogallol structures, while the DPPH assay was mainly determined by the number of OH groups.

Plants produce a diverse array of secondary metabolites that are generally nonessential but facilitate ecological interactions. Fruits, vegetables, seeds and nuts can accumulate bioactive secondary metabolites with health-promoting properties, including the potent antioxidant activities of phenolic compounds. Several in vitro assays have been developed to measure the polyphenol content and antioxidant activity of plant extracts, e.g., the simple and highly popular Folin-Ciocalteu (FC) assay. However, the literature contains a number of different descriptions of the assay and it is unclear whether the assay measures the polyphenol content or reducing capacity of the sample. To determine the influence of phenolic structures on the outcome of the FC assay, we tested phenols representing different subgroups (phenolic acids, flavonols, flavanols, dihydrochalcones and flavanones). We observed different results for each reference substance and subgroup. Accordingly, we concluded that the FC assay does not measure the polyphenol content of a sample but determines its reducing capacity instead. Assigning the substances to five structural classes showed that the FC results depend on the number of fulfilled Bors criteria. If a molecule fulfills none of the Bors criteria, the FC results depend on the number of OH groups. We did not find a correlation with other single electron transfer assays (e.g., ABTS and DPPH assays). Furthermore, the FC assay was compatible with all five subgroups and should be preferred over the DPPH assay, which is specific for extracts rich in dihydrochalcones or flavanones.

Increasingly restricted availability and environmental impact of mineral oils have boosted the interest in sustainable lubrication. In this study, the thickening properties of sodium carboxymethyl celluloses (CMCs) were investigated in order to assess their potential as viscosity modifiers in aqueous gear and bearing fluids. The pressure, temperature and shear dependence of viscosity was studied at different concentrations and molecular weights $M_W$. The tribological properties were investigated at different viscosity grades in both sliding and rolling contact, and compared to rapeseed oil and polyethylene glycol 400. The viscosity of the CMC solutions was adjustable to all application-relevant viscosity grades. Viscosity indices were similar or higher compared to the reference fluids and mineral oil. Temporary and permanent viscosity losses increased with $M_W$. Permanent viscosity loss was highest for high $M_W$ derivatives, up to 70%. The pressure-viscosity coefficients $\alpha$ were low and showed a high dependency on shear and concentration. In rolling contact, low $M_W$ CMC showed up to 35% lower friction values compared to high $M_W$, whereas no improvement of lubricating properties was observed in sliding contact. The results suggest that low $M_W$ CMC has great potential as bio-based thickener in aqueous lubrication.

Flexible organic electronic devices are often protected from degradation by encapsulation in multilayered films with very high barrier properties against moisture and oxygen. However, metrology must be improved to detect such low quantities of permeants. We therefore developed a modified ultra-low permeation measurement device based on a constant-flow carrier-gas system to measure both the transient and stationary water vapor permeation through high-performance barrier films. The accumulation of permeated water vapor before its transport to the detector allows the measurement of very low water vapor transmission rates (WVTRs) down to 2 × 10⁻⁵ g m⁻² d⁻¹. The measurement cells are stored in a temperature-controlled chamber, allowing WVTR measurements within the temperature range 23–80 °C. Differences in relative humidity can be controlled within the range 15%–90%. The WVTR values determined using the novel measurement device agree with those measured using a commercially available carrier-gas device from MOCON^®. Depending on the structure and quality of the barrier film, it may take a long time for the WVTR to reach a steady-state value. However, by using a combination of the time-dependent measurement and the finite element method, we were able to estimate the steady-state WVTR accurately with significantly shorter measurement times.