Polymer Brush Friction in Cylindrical Geometries

Polymer brushes are outstanding lubricants that can strongly reduce wear and friction between surfaces in sliding motion. In recent decades, many researchers have put great effort in obtaining a clear understanding of the origin of the lubricating performance of these brushes. In particular, molecular dynamics simulations have been a key technique in this scientific journey. They have given us a microscopic interpretation of the tribo-mechanical response of brushes and have led to the prediction of their shear-thinning behavior, which has been shown to agree with experimental observations. However, most studies so far have focused on parallel plate geometries, while the brush-covered surfaces might be highly curved in many applications. Here, we present molecular dynamics simulations that are set up to study the friction for brushes grafted on the exterior of cylinders that are moving inside larger cylinders that bear brushes on their interior. Our simulations show that the density distributions for brushes on the interior or exterior of these cylinders are qualitatively different from the density profiles of brushes on flat surfaces. In agreement with theoretical predictions, we find that brushes on the exterior of cylinders display a more gradual decay, while brushes on the interior of cylinders becomes denser compared to flat substrates. When motion is imposed, the density profiles for cylinder-grafted brushes adapt qualitatively differently to the shear motion than observed for the parallel plate geometry: the zone where brushes overlap moves away from its equilibrium position. Surprisingly, and despite all these differences, we observe that the effective viscosity is independent of the radius of the brush-grafted cylinders. The reason for this is that the viscosity is determined by the overlap between the brushes, which turns out to be insensitive to the exact density profiles. Our results provide a microscopic interpretation of the friction mechanism for polymer brushes in cylindrical geometries and will aid the design of effective lubricants for these systems

Presence and risks of polycyclic aromatic hydrocarbons, dioxins and dioxin-like PCBs in dietary plant supplements as elucidated by a combined DR CALUX® bioassay and GC-HRMS based approach

Plant-based dietary supplements may contain undesirable contaminants such as polycyclic aromatic hydrocarbons, dioxins and dioxin-like polychlorinated biphenyls (dl-PCBs) due to the sources of raw materials or processing methods used. The presence of these contaminants in a series of herbal supplements sold on the Ghanaian market for improving sexual performance was examined using the DR CALUX® bioassay in combination with GC-HRMS analysis. Overall, cell responses at 4 and 48 h exposure to extracts prepared without an acid-silica clean-up were relatively higher than the responses obtained from extracts prepared with an acid-silica clean-up. This indicated that the 40 supplements contained only low levels of stable aryl hydrocarbon receptor (AhR) agonists like polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and dl-PCBs, while some contained substantial amounts of less stable AhR-agonists. Ten supplements selected for confirmation with GC-HRMS analysis contained PCDD/Fs and dl-PCBs at levels ranging from 0.01 to 0.19 pg toxic equivalent (TEQ)/g only, while the level of the sum of 4 polycyclic aromatic hydrocarbons (Σ4PAHs) representing less stable AhR agonists, ranged from not detected (ND) to 25.5 ng/g. These concentrations were in line with the responses observed in the DR CALUX® bioassay. The concentration of PCDD/Fs and dl-PCBs corresponded to estimated daily intakes (EDIs) ranging from 0.01 to 1.20 pg TEQ/day, or 0.001 to 0.12 pg TEQ/kg bw/week for a 70 kg bw consumer, which was below the established tolerable weekly intake (TWI) of 2 pg TEQ/kg bw/week, thus indicating low concern for consumers’ health. Similarly, the EDIs based on the detected Σ4PAHs in supplements ranged from 7.2 to 111 ng/day, or 0.1 to 1.6 ng/kg bw/day, which corresponded to MOE values above 10,000, indicating a low health concern

Detection and Characterization of Ignitable Liquid Residues in Forensic Fire Debris Samples by Comprehensive Two-Dimensional Gas Chromatography

This study covers an extensive experimental design that was developed for creating simulated fire debris samples under controlled conditions for the detection and identification of ignitable liquids (IL) residues. This design included 19 different substrates, 45 substrate combinations with and without ignitable liquids, and 45 different ILs from three classes (i.e., white spirit, gasoline, and lamp oil). Chemical analysis was performed with comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GC×GC-TOFMS) for improved separation and compound identification. The enhanced peak capacity offered by GC×GC-TOFMS allowed the use of a target compound list in combination with a simple binary decision model to arrive at quite acceptable results with respect to IL detection (89% true positive and 7% false positive rate) and classification (100% correct white spirit, 79% correct gasoline, and 77% correct lamp oil assignment). Although these results were obtained in a limited set of laboratory controlled fire experiments including only three IL classes, this study confirms the conclusions of other studies that GC×GC-TOFMS can be a powerful tool in the challenging task of forensic fire debris analysis