Differential scanning calorimetric study of the interaction of 2,2′-dibenzothiazole,sulfur, zinc oxide,and stearic acid in the presence of polyisoprene

The interactions between mixtures of 2,2'-dibenzothiazole (MBTS), sulfur, ZnO, and stearic acid were studied by DSC in the presence of polyisoprene (IR). In the absence of ZnO, the onset of vulcanization was at a lower temperature than in its presnece, and the crosslink densities were relatively low. ZnO as well as stearic acid did not influence the consumption of MBTS, but the amount of MBT in the sample after vulcanization increased in the presence of ZnO and still more when ZnO and stearic acid were present—the same applied for the crosslink densities. In view of these results, interaction mechanisms are proposed for the different systems.     

Clotting Phenomena at the Blood-Polymer Interface and Development of Blood Compatible Polymeric Surfaces

In the past two decades many attempts have been made to relate surface and interfacial parameters with the blood compatibility of polymeric surfaces. It is however doubtful if by a single parameter the behaviour of blood on a surface can be predicted. Two major aspects of blood compatibility—the prevention of platelet adhesion and the deactivation of the intrinsic coagulation system are determined by the measure and nature of competitive blood protein adsorption on the foreign surface. The adhesion of blood platelets is promoted by adsorbed fibrinogen and gamma globulin, while adsorbed albumin inhibits platelet adhesion. Heparinised surfaces do not adsorb fibrin and consequently no adhesion of platelets takes place. Other surfaces with low platelet adhesion are the hydrogels, certain block copolyetherurethanes, polyelectrolyte complexes and biolised proteins. Heparinised surfaces of the cationically bonded type inhibit the intrinsic coagulation as well, however this may be due to unstable coatings and heparin leakage. In the authors laboratory a synthetic heparinoid was prepared with the structure - [CH₂ - C(CH₃ NHSO₃ Na - C(H) COONa - CH₂ -] x? with M?_w = (7.5 /pm 1.0) × 10⁵ and an in vivo anticoagulant activity of 50% of heparin. Its coatings on PVC, using tridodecylmethyl-ammonium chloride as a coupling agent, are stable in plasma and salt solutions and provide surfaces which show negligible platelet adhesion and a strong inhibition of the intrinsic coagulation on contact with blood. Similar results were found with polydimethylsiloxane surfaces coated with this heparinoid.     

Wood‐induced backwater effects in lowland streams

Placement of wood in streams has become a common method to increase ecological value in river and stream restoration and is widely used in natural environments. Water managers, however, are often hesitant to introduce wood in channels that drain agricultural and urban areas because of backwater effect concerns. This study aims to better understand the dependence of wood‐induced backwater effects on cross‐sectional area reduction and on discharge variation. A newly developed, one‐dimensional stationary model demonstrates how a reduction in water level over the wood patch significantly increases directly after wood insertion. The water level drop is found to increase with discharge, up to a maximum level. If the discharge increases beyond this maximum, the water level drop reduces to a value that may represent the situation without wood. This reduction predominately depends on the obstruction ratio, calculated as the area covered by wood in the channel cross section divided by the total cross‐sectional area. The model was calibrated with data from a field study in four lowland streams in the Netherlands. The field study showed that morphologic adjustments in the stream and reorientation of the woody material reduced the water level reduction over the patches in time. The backwater effects can thus be reduced by optimizing the location where wood patches are placed and by manipulating the obstruction ratio. The model can function as a generic tool to achieve a stream design with wood that optimizes the hydrological and ecological potential of streams.     

Nanocomposites Based on Polyethylene and Polyhedral Oligomeric Silsesquioxanes, 1 – Microstructure,Thermal and Thermomechanical Properties

Nanocomposites of linear low‐density polyethylene (LLDPE), with three different amounts of polyhedral oligomeric silsesquioxanes (POSS), were prepared through melt‐mixing in a batch‐mixer at 150 °C. The structure of the prepared nanocomposites was studied by X‐ray scattering and optical microscopy. The surface morphology of the nanocomposites was investigated through field‐emission SEM. The thermal properties of the pure LLDPE and nanocomposites were studied by differential scanning calorimeter (DSC). Thermomechanical properties were assessed on a Paar‐Physics MCR501 rheometer using a solid‐state rectangular fixture. Results exhibited a significant improvement in both the storage and loss moduli of the neat LLDPE upon the incorporation of the POSS particles. A substantial improvement in thermal stability was also observed in the high‐temperature region.

     

Relationship between magnetic field strength and magnetic-resonance-related acoustic noise levels

The need for better signal-to-noise ratios and resolution has pushed magnetic resonance imaging (MRI) towards high-field MR-scanners for which only little data on MR-related acoustic noise production have been published. The purpose of this study was to validate the theoretical relationship of sound pressure level (SPL) and static magnetic field strength. This is relevant for allowing adequate comparisons of acoustic data of MR systems at various magnetic field strengths. Acoustic data were acquired during various pulse sequences at field strengths of 0.5, 1.0, 1.5 and 2.0 Tesla using the same MRI unit by means of a Helicon rampable magnet. Continuous-equivalent, i.e. time-averaged, linear SPLs and 1/3-octave band frequencies were recorded. Ramping from 0.5 to 1.0 Tesla and from 1.0 to 2.0 Tesla resulted in an SPL increase of 5.7 and 5.2 dB(L), respectively, when averaged over the various pulse sequences. Most of the acoustic energy was in the 1-kHz frequency band, irrespective of magnetic field strength. The relation between field strength and SPL was slightly non-linear, i.e. a slightly less increase at higher field strengths, presumably caused by the elastic properties of the gradient coil encasings. Electronic Publication     

The Role of Target Binding Kinetics in Drug Discovery

Traditionally structure–activity/affinity relationships (SAR) have dominated research in medicinal chemistry. However, structure–kinetics relationships (SKR) can be very informative too. In this viewpoint we explore the molecular determinants of binding kinetics and discuss challenges for future binding kinetics studies. A scheme for future kinetics‐directed drug design and discovery is also proposed.     

Latex derived blends of poly(vinyl acetate) and natural rubber: thermal and mechanical properties

Poly(vinyl acetate) (PVAc) and natural rubber blends (NR) were prepared by low shear blending of the corresponding lattices. Thin films were cast using a doctor blade technique. SEM and DMA confirmed the essential immiscibility of the two polymers. Even when the poly(vinyl acetate) forms the matrix phase, it still contains domains encapsulated by a rubber phase where particles that resemble the original latex are visible. This incomplete droplet coalescence of the poly(vinyl acetate) is attributed to the fact that the rubber latex droplets were an order of magnitude smaller than the poly(vinyl acetate) latex droplets. Tensile testing revealed a nonlinear dependence of tensile strength and elongation on blend composition. Surprisingly good tensile yield strengths were obtained at intermediate to high PVAc contents. Thermogravimetric analysis of degradation in air and nitrogen atmospheres indicated independent degradation of the parent polymers.     

Performance of metal alloys as hydrogen evolution reaction catalysts in a microbial electrolysis cell

H₂ can be produced from organic matter with a microbial electrolysis cell (MEC). To decrease the energy input and increase the H₂ production rate of an MEC, a catalyst is used at the cathode. Platinum is an effective catalyst, but its high costs stimulate searching for alternatives, such as non-noble metal alloys. This study demonstrates that copper sheet coated with nickel-molybdenum, nickel-iron-molybdenum or cobalt-molybdenum alloys have a higher catalytic activity for the hydrogen evolution reaction than nickel cathodes, measured near neutral pH. However, the catalytic activity cannot be fully exploited near neutral pH because of mass transport limitation. The catalytic activity is best exploited at alkaline pH where mass transport is not limiting. This was demonstrated in an MEC with a cobalt-molybdenum coated cathode and anion exchange membrane, which produced 50 m³ H₂ m⁻³ MEC d⁻¹ (at standard temperature and pressure) at an electricity input of 2.5 kWh m⁻³ H₂.