Effect of Creep and Aging on the Precipitation Kinetics of an Al–Cu Alloy after One Pass of ECAP

Recent work shows that severe plastic deformation processes such as ECAP or HPT considerably accelerate the precipitation kinetics of Al‐Cu alloys. In this study, the authors analyze how a combination of mechanical load, aging time (and increased plastic strain), and aging temperature affects the precipitation kinetics of an AA2017 alloy after ECAP. After solution annealing, the material is processed by one pass of ECAP (120°‐channel angle) at 140 °C. Compressive creep tests are performed on the initial condition and the ECAP‐deformed material. The resulting microstructures are studied in detail using electron microscopy. To investigate the influence of mechanical loading, interrupted compressive creep tests are performed and compared with aged samples (produced without any mechanical loading at the same temperature and after the same amount of time). By keeping time and load constant in another set of interrupted compressive creep tests, the influence of temperature is investigated. Our study shows that increasing mechanical loading further accelerates the precipitation kinetics. Temperature accelerates the precipitation kinetics as well, but results in coarser precipitates. The authors also find that different creep strains can lead to the formation of two different regions in the microstructure: regions with only a few coarsened θ‐phase precipitates, and regions with numerous, finely dispersed precipitates.     

Identification of Drugs Inducing Phospholipidosis by Novel in vitro Data

Drug‐induced phospholipidosis (PLD) is a lysosomal storage disorder characterized by the accumulation of phospholipids within the lysosome. This adverse drug effect can occur in various tissues and is suspected to impact cellular viability. Therefore, it is important to test chemical compounds for their potential to induce PLD during the drug design process. PLD has been reported to be a side effect of many commonly used drugs, especially those with cationic amphiphilic properties. To predict drug‐induced PLD in silico, we established a high‐throughput cell‐culture‐based method to quantitatively determine the induction of PLD by chemical compounds. Using this assay, we tested 297 drug‐like compounds at two different concentrations (2.5 μM and 5.0 μM ). We were able to identify 28 previously unknown PLD‐inducing agents. Furthermore, our experimental results enabled the development of a binary classification model to predict PLD‐inducing agents based on their molecular properties. This random forest prediction system yields a bootstrapped validated accuracy of 86 %. PLD‐inducing agents overlap with those that target similar biological processes; a high degree of concordance with PLD‐inducing agents was identified for cationic amphiphilic compounds, small molecules that inhibit acid sphingomyelinase, compounds that cross the blood–brain barrier, and compounds that violate Lipinski’s rule of five. Furthermore, we were able to show that PLD‐inducing compounds applied in combination additively induce PLD.     

Acoustophoresis of hollow and core-shell particles in two-dimensional resonance modes

Motivated by the applications of ultrasonic particle manipulation in a biotechnological context, a study on acoustophoresis of hollow and core-shell particles is presented with analytical derivations, numerical simulations and confirming experiments. For a long-wavelength calculation of the acoustic radiation forces, the Gor’kov potential of hollow, air-filled particles and particles with solid or fluid core and shell is derived. The validity as well as the applicable range of the long-wavelength calculation is evaluated with numerical simulations in Comsol Multiphysics^®. The results are experimentally verified in the acoustic field of an intrinsically two-dimensional fluid resonance mode, which allows for a more complex analysis than the common one-dimensional ultrasonic standing waves or their superposition to two-dimensional fields. Experiments were conducted with hollow glass particles (13.9 μm diameter) in a microfluidic chamber of 1.2 mm × 1.2 mm × 0.2 mm on a silicon-based device with piezoelectric excitation around 870 kHz. The described resonance mode is of additional interest for particle trapping and medium exchange on certain particle types, and it reveals a novel approach for particle characterization or separation.     

Graph-regularized 3D shape reconstruction from highly anisotropic and noisy images

Analysis of microscopy images can provide insight into many biological processes. One particularly challenging problem is cellular nuclear segmentation in highly anisotropic and noisy 3D image data. Manually localizing and segmenting each and every cellular nucleus is very time-consuming, which remains a bottleneck in large-scale biological experiments. In this work, we present a tool for automated segmentation of cellular nuclei from 3D fluorescent microscopic data. Our tool is based on state-of-the-art image processing and machine learning techniques and provides a user-friendly graphical user interface. We show that our tool is as accurate as manual annotation and greatly reduces the time for the registration.     

Equilibrium sampling of freely dissolved alkylphenols into a thin film of 1-octanol supported on a hollow fiber membrane

A new negligible depletion extraction procedure was proposed for equilibrium sampling of 4-tert-octylphenol (OP) and 4-nonylphenol (NP) into a thin film of 1-octanol supported on a hollow fiber membrane. This thin liquid film extraction technique was directed at the determination of (1) freely dissolved concentrations, (2) distribution coefficients to 1-octanol (D(ow)), and (3) binding to dissolved organic matter (DDOC). The sampling device was prepared by dipping pieces of polypropylene microporous hollow fiber membrane (10-mm length, 30-microm wall thickness, 240-microm inner diameter) into 1-octanol for a few seconds to impregnate the pores of the hollow fiber wall. After stirring in 100 mL of sample solution for 24 h, the sampling device was harvested and desorbed with 30 microL of methanol, of which 20 microL was injected for HPLC analysis. With the measured D(ow) of a chemical and its equilibrium concentration in the 1-octanol sampling phase (C(octanol)), the freely dissolved concentration (Cfree) was calibrated based on Cfree = C(octanol)/D(ow). Measured log Dow values of OP (4.32 +/- 0.06) and NP (4.79 +/- 0.02) were independent of the chemical concentration, only minimally affected by the environmentally relevant pH, buffering capacity, and salinity of samples, and agreed well with reported values. Log DDOC values of OP (4.89 +/- 0.43) and NP (5.14 +/- 0.37), determined in Aldrich humic acid solution, agreed with reported partition coefficients to organic carbon (log Koc) for particles in river water and effluent wastewater. Short equilibration times and high enrichment factors were obtained for both analytes due to the high surface to volume ratio of the new sampler. The technique was successfully applied to determine Cfree of OP and NP in real water samples and to study their association with humic acids and bovine albumin.     

Nanoparticle traffic on helical tracks: thermophoretic mass transport through carbon nanotubes

Using molecular dynamics simulations, we demonstrate and quantify thermophoretic motion of solid gold nanoparticles inside carbon nanotubes subject to wall temperature gradients ranging from 0.4 to 25 K/nm. For temperature gradients below 1 K/nm, we find that the particles move "on tracks" in a predictable fashion as they follow unique helical orbits depending on the geometry of the carbon nanotubes. These findings markedly advance our knowledge of mass transport mechanisms relevant to nanoscale applications.     

Long-term and long-range migration of radioactive fallout in a Karst system

Mountainous areas are often covered by little evolved soils from which deposited radionuclides can potentially leak into the vadose zone. In the Swiss Jura mountains, we observed unusual isotopic ratios of nuclear weapon test (NWTs) fallout with an apparent loss of NWTs plutonium relative to 13?Cs of Chernobyl origin in thinner soils. Here, we studied the karstic watershed of a vauclusian spring to determine the residence times of plutonium, 2?1Am, and ??Sr deposited by global fallout and their respective mobility in carbonaceous soils. The results show that ??Sr is washed most efficiently from the watershed with a residence time of several hundred years. The estimated plutonium residence time is more than 10 times higher (in the range of 5000-10,000 years), and the 2?1Am residence time is double that of plutonium. The spring water 2?1Am/23?+2??Pu isotopic ratio is lower (0.12 - 0.28) than found in watershed soils (0.382 ± 0.077). Similar differences are found in aquatic mosses (2?1Am/23?+2??Pu isotopic ratio 0.05-0.12), which are permanently submerged in spring waters. In contrast to plutonium, ??Sr is leached from these mosses with 0.5M HCl, demonstrating that strontium is probably associated with calcium carbonate precipitations on the mosses. The higher plutonium to americium isotopic ratio found in the samples of spring water and mosses at the outlet of the karst shows that plutonium mobility is enhanced.     

Piezoresistive properties of PEDOT:PSS

Recent market studies mention the necessity to include sensors in the design of organic electronic devices in order to broaden the range of applications. It is therefore essential to identify potential organic mechanical sensor materials and to develop processes and methods to structure them and characterize their piezoresistive properties. Furthermore, it is also essential for organic electronic devices to know the change of resistance upon bending of flexible substrates. A material widely used in organic electronics is the complex of the intrinsically conductive polymer poly(3,4-ethylenedioxythiophene) and polystyrene sulfonate acid (PEDOT/PSS). In this paper first the fabrication of a polyimide (PI) membrane with integrated PEDOT/PSS strain gauges is presented. Upon a pressure difference the membrane is deflected and the resulting changes in resistance of the sensor elements are recorded. By applying a membrane mechanics model the resistance changes can be linked to the strain in the membrane and then the plane strain gauge factor k_PS for PEDOT/PSS of 0.48±0.07 at 36.6±3% rH can be determined.     

Passive dosing of soil invertebrates with polycyclic aromatic hydrocarbons: limited chemical activity explains toxicity cutoff

The partitioning of organic soil pollutants into soil organisms is driven by their chemical activity, which normally does not exceed that of the pure pollutant. Passive dosing with the silicone poly(dimethylsiloxane) (PDMS) was used to initiate and maintain the maximum chemical activity of 10 polycyclic aromatic hydrocarbons (PAHs) in toxicity tests with the springtail Folsomia candida. The test animals could move freely on the PDMS saturated with PAHs, resulting in direct contact and exposure to saturated air. After 7 days, springtail lethality correlated neither with the octanol-water partition coefficients of the PAHs nor with their molecular size, but with their melting point All low-melting PAHs (T(M) < or = 110 degrees C) caused 100% lethality, whereas all high-melting PAHs (TM > or = 180 degrees C) caused no significant lethality. The lethality was successfully fitted to one chemical activity response curve for all PAHs tested, with effective chemical activity causing 50% lethality (Ea-50) of 0.058. It was also fitted to the PAH concentration in the PDMS, resulting in an EC(PDMS)-50 of 8.7 mM. Finally, the combined exposure to anthracene and pyrene was described by the sum of chemical activities causing lethality, in good agreement with the chemical activity-response curve obtained.