Dynamics of coaxial torsional resonators consisting or segments with different radii,material properties and surrounding media

High-Q torsional resonators constitute the most sensitive transducers for high frequency dynamic viscoelastic measurements of dilute polymer solutions. Most such resonators described in the literature are segmented. Because of the need for torque and torsional displacement transducers the Q-value of the individual segments most often differ, but normally all segments have the same radius.A detailed analysis of the dynamics of such resonators when both the radii, material properties and surrounding media may be different for each segment, is presented. For resonators where all segment lengths equal an integer multiple of a quarter of the torsional wavelength, we find that the Q-value of the resonator as a whole is mainly determined by the Q-value of the segment with the smallest radius. We further find that reduction of the radius of the segment surrounded by polymer solution results in a stronger mechanical coupling between the resonator as a whole and the polymer solution. These findings suggest that the segment radii are important optimization parameters of segmented torsional resonators used to measure the high frequency dynamic viscoelastic properties of e.g. polymer solutions.     

Solvent effects on the n-->pi* electronic transition in formaldehyde: a combined coupled cluster/molecular dynamics study

We present a study of the blueshift of the n-->pi* electronic transition in formaldehyde in aqueous solution using a combined coupled cluster/molecular mechanics model including mutual polarization effects in the Hamiltonian. In addition, we report ground and excited state dipole moments. Configurations are generated from molecular dynamics simulations with two different force fields, one with and one without an explicit polarization contribution. A statistical analysis using 1200 configurations is presented. Effects of explicit polarization contributions are found to be significant. It is found that the main difference in the effects on the excitation energies arises from the fact that the two force fields result in different liquid structures, and thus a different set of configurations is generated for the coupled cluster/molecular mechanics calculations.     

Microfluidic capturing-dynamics of paramagnetic bead suspensions

We study theoretically the capturing of paramagnetic beads by a magnetic field gradient in a microfluidic channel treating the beads as a continuum. Bead motion is affected by both fluidic and magnetic forces. The transfer of momentum from beads to the fluid creates an effective bead-bead interaction that greatly aids capturing. We demonstrate that for a given inlet flow speed a critical density of beads exists above which complete capturing takes place.     

Electro-hydrodynamic propulsion of counter-rotating Pickering drops

Insulating particles or drops suspended in carrier liquids may start to rotate with a constant frequency when subjected to a uniform DC electric field. This is known as the Quincke rotation electro-hydrodynamic instability. A single isolated rotating particle exhibit no translational motion at low Reynolds number, however interacting rotating particles may move relative to one another. Here we present a simple system consisting of two interacting and deformable Quincke rotating particle covered drops, i.e. deformable Pickering drops. The drops attract one another and spontaneously form a counter-rotating pair that exhibits electro-hydrodynamic driven propulsion at low Reynolds number flow.     

Experimental investigation of wake evolution behind a couple of flat discs in a hydrochannel

The decay of a far wake and its turbulent fluctuations behind two thin discs of the same diameter D, oriented normal to the incident flow, have been studied using the Particle Image Velocimetry (PIV). The experimental study was carried out in a water flume (Re ≈ 2·10⁵) with varying distances between the discs (L _х = 4–8D) and their axes shift relative to each other (0, 0.5D and 1D). It is found that the velocity deficit behind two discs depends weakly on L _x , and at L _х > 40D, it becomes indistinguishable from the level of turbulent fluctuations of the incident flow. It is found that the decay of the average velocity deficit and its turbulent fluctuations in a wake of a tandem of discs can be described by the same analytical dependence with exponent–2/3 as for the wake decay of a single disc. However, at the same distance downstream, the value of deficit behind two discs is substantially higher than the corresponding value behind a single disc. Velocity fluctuations in a far wake behind a pair of discs depend weakly on longitudinal dimension L _x , but at the same time, in contrast to the velocity deficit, their level does not differ significantly from the level of fluctuations behind a single disc.     

Ethanol Production from Wet-Exploded Wheat Straw Hydrolysate by Thermophilic Anaerobic Bacterium Thermoanaerobacter BG1L1 in a Continuous Immobilized Reactor

Thermophilic ethanol fermentation of wet-exploded wheat straw hydrolysate was investigated in a continuous immobilized reactor system. The experiments were carried out in a lab-scale fluidized bed reactor (FBR) at 70°C. Undetoxified wheat straw hydrolysate was used (3–12% dry matter), corresponding to sugar mixtures of glucose and xylose ranging from 12 to 41 g/l. The organism, thermophilic anaerobic bacterium Thermoanaerobacter BG1L1, exhibited significant resistance to high levels of acetic acid (up to 10 g/l) and other metabolic inhibitors present in the hydrolysate. Although the hydrolysate was not detoxified, ethanol yield in a range of 0.39–0.42 g/g was obtained. Overall, sugar efficiency to ethanol was 68–76%. The reactor was operated continuously for approximately 143 days, and no contamination was seen without the use of any agent for preventing bacterial infections. The tested microorganism has considerable potential to be a novel candidate for lignocellulose bioconversion into ethanol. The work reported here also demonstrates that the use of FBR configuration might be a viable approach for thermophilic anaerobic ethanol fermentation.     

Controlling Two‐Step Multimode Switching of Dihydroazulene Photoswitches

We present the synthesis and switching studies of systems with two photochromic dihydroazulene (DHA) units connected by a phenylene bridge at either para or meta positions, which correspond to a linear or cross‐conjugated pathway between the photochromes. According to UV/Vis absorption and NMR spectroscopic measurements, the meta‐phenylene‐bridged DHA–DHA exhibited sequential light‐induced ring openings of the two DHA units to their corresponding vinylheptafulvenes (VHFs). Initially, the VHF–DHA species was generated, and, ultimately, after continued irradiation, the VHF–VHF species. Studies in different solvents and quantum chemical calculations indicate that the excitation of DHA–VHF is no longer a local DHA excitation but a charge‐transfer transition that involves the neighboring VHF unit. For the linearly conjugated para‐phenylene‐bridged dimer, electronic communication between the two units is so efficient that the photoactivity is reduced for both the DHA–DHA and DHA–VHF species, and DHA–DHA, DHA–VHF, and VHF–VHF were all present during irradiation. In all, by changing the bridging unit, we can control the degree of stepwise photoswitching.     

Aromaticity‐Controlled Energy Storage Capacity of the Dihydroazulene‐Vinylheptafulvene Photochromic System

Photochemical conversion of molecules into high‐energy isomers that, after a stimulus, return to the original isomer presents a closed‐cycle of light‐harvesting, energy storage, and release. One challenge is to achieve a sufficiently high energy storage capacity. Here, we present efforts to tune the dihydroazulene/vinylheptafulvene (DHA/VHF) couple through loss/gain of aromaticity. Two derivatives were prepared, one with aromatic stabilization of DHA and the second of VHF. The consequences for the switching properties were elucidated. For the first type, sigmatropic rearrangements of DHA occurred upon irradiation. Formation of a VHF complex could be induced by a Lewis acid, but addition of H₂O resulted in immediate regeneration of DHA. For the second type, the VHF was too stable to convert into DHA. Calculations support the results and provide new targets. We predict that by removing one of the two CN groups at C‐1 of the aromatic DHA, the heat storage capacity will be further increased, as will the life‐time of the VHF. Calculations also reveal that a CN group at the fulvene ring retards the back‐reaction, and we show synthetically that it can be introduced regioselectively.     

One-dimensional corrugation of the h-BN monolayer on Fe(110)

We report on a new nanopatterned structure represented by a single atomic layer of hexagonal boron nitride (h-BN) forming long periodic waves on the Fe(110) surface. The growth process and the structure of this system are characterized by X-ray absorption (XAS), core-level photoemission spectroscopy (CL PES), low-energy electron microscopy (LEEM), microbeam low-energy electron diffraction (μLEED), and scanning tunneling microscopy (STM). The h-BN monolayer on Fe(110) is periodically corrugated in a wavy fashion with an astonishing degree of long-range order, periodicity of 2.6 nm, and the corrugation amplitude of ～0.8 ?. The wavy pattern results from a strong chemical bonding between h-BN and Fe in combination with a lattice mismatch in either [111] or [111] direction of the Fe(110) surface. Two primary orientations of h-BN on Fe(110) can be observed corresponding to the possible directions of lattice match between h-BN and Fe(110), with approximately equal area of the boron nitride domains of each orientation.