Prelabeling Expansion Single-Molecule Localization Microscopy with Minimal Linkage Error

Expansion microscopy combined with single-molecule localization microscopy (ExSMLM) has a potential for approaching molecular resolution. However, ExSMLM faces multiple challenges such as loss of fluorophores and proteins during polymerization, digestion or denaturation, and an increase in linkage error arising from the distance between the fluorophore and the target molecule. Here, we introduce a trifunctional streptavidin to link the target, fluorophore and gel matrix via a biotinylizable peptide tag. The resultant ExSMLM images of vimentin filaments demonstrated high labeling efficiency and a minimal linkage error of ∼5 nm. Our ExSMLM provides a simple and practical means for fluorescence imaging with molecular resolution.     

Effects of Rare Earth Metal addition on the cavitation erosion-corrosion resistance of super duplex stainless steels

Austenitic stainless steels such as AISI 316L have been used in equipment in which fluid flows at high speeds which can induce cavitation erosion on metallic surfaces due to the collapse of cavities, where the collapse is caused by the sudden change of local pressure within the liquid. Usually AISI 316L is susceptible to cavitation erosion. This research focuses on developing a better material to replace the AISI 316L used in equipment with high speed fluid flow, such as impellers. The effects of Rare Earth Metal (REM) additions on the cavitation erosion-corrosion resistance of duplex stainless steels were studied using metallographic examination, the potentiodynamic anodic polarization test, the tensile test, the X-ray diffraction test and the ultrasonic cavitation erosion test. The experimental alloys were found to have superior mechanical properties due to interstitial solid solution strengthening, by adding high nitrogen (0.4%), as well as by the refinement of phases and grains induced by fine REM oxides and oxy-sulfides. Corrosion resistance decreases in a gentle gradient as the REM content increases. However, REM containing alloys show superior corrosion resistance compared with that of other commercial alloys (SAF 2507, AISI 316L). Owing to their excellent mechanical properties and corrosion resistance, the alloys containing REM have high cavitation erosion-corrosion resistance.     

Effect of Time-Dependent Pinning Pressure on Abnormal Grain Growth: Phase Field Simulation

The effect of the time-dependent pinning pressure of precipitates on abnormal grain growth has been investigated by multiphase field simulation with a simple precipitation model. The application of constant pinning pressure is problematic because it always induces abnormal grain growth or no grain growth, which is not reasonable considering the real situation. To produce time-dependent pinning pressure, both precipitation kinetics and precipitate coarsening kinetics have been considered with two rates: slow and fast. The results show that abnormal grain growth is suppressed at the slow precipitation rate. At the slow precipitation rate, the overall grain growth caused by the low pinning pressure in the early stage indeed plays a role in preventing abnormal grain growth by reducing the mobility advantage of abnormal grains. In addition, the fast precipitate coarsening rate tends to more quickly transform abnormal grain growth into normal grain growth by inducing the active growth of grains adjacent to the abnormal grains in the early stage. Therefore, the present study demonstrates that the time dependence of the pinning pressure of precipitates is a critical factor that determines the grain growth mode.     

Liquid-phase degradation of polyethylene wax over mordenite catalysts with different Si/Al molar ratios

The catalytic liquid-phase degradation of polyethylene wax into fuel oil was studied using mordenite catalysts with various Si/Al molar ratios prepared by dealumination. The total yield of gas and liquid products showed a volcano plot along the Si/Al molar ratio of mordenite. No significant change was observed in the composition of the liquid product for all catalysts used in this study. Fast deactivation was anticipated on the mordenite catalysts with low Si/Al molar ratios such as 5 and 10, due to pore blocking by the carbon deposited on the external surface of the zeolite. A high activity and a long catalyst life were obtained on the mordenite catalyst with a Si/Al molar ratio of 12.     

Estimating Clock Uncertainty for Efficient Duty-Cycling in Sensor Networks

Radio duty cycling has received significant attention in sensor networking literature, particularly in the form of protocols for medium access control and topology management. While many protocols have claimed to achieve significant duty-cycling benefits in theory and simulation, these benefits have often not translated into practice. The dominant factor that prevents the optimal usage of the radio in real deployment settings is time uncertainty between sensor nodes which results in overhead in the form of long packet preambles, guard bands, and excessive control packets for synchronization. This paper proposes an uncertainty-driven approach to duty-cycling, where a model of long-term clock drift is used to minimize the duty-cycling overhead. First, we use long-term empirical measurements to evaluate and analyze in-depth the interplay between three key parameters that influence long-term synchronization: synchronization rate, history of past synchronization beacons, and the estimation scheme. Second, we use this measurement-based study to design a rate-adaptive, energy-efficient long-term time synchronization algorithm that can adapt to changing clock drift and environmental conditions, while achieving application-specific precision with very high probability. Finally, we integrate our uncertainty-driven time synchronization scheme with the BMAC medium access control protocol, and demonstrate one to two orders of magnitude reduction in transmission energy consumption with negligible impact on packet loss rate.     

Mixed Dimensional Coupling in Finite Element Stress Analysis

Many analysis models utilize finite elements of reduced dimension. However, to capture stress concentrations at local details, it would be desirable to combine the reduced dimensional element types with higher dimensional elements in a single finite element model. It is therefore important in such cases to integrate into the analyses some scheme for coupling the element types that conforms to the governing equations of the problem. In this paper, a novel method that can correctly couple beams to solids, beams to shells and shells to solids for elastic problems is presented. The approach adopted is to equate the work done on either side of the interface between dimensions, and this leads to multi-point constraint equations, thus providing a relationship among nodal degrees of freedom between the differing element types. Example results show that the proposed technique does not introduce any spurious stresses at the dimensional interfaces. ID="A1" Correspondence and offprint requests to: C. G. Armstrong, School of Mechanical and Manufacturing Engineering, The Queen's University of Belfast, Ashby Building, Stranmillis Road, Belfast BT9 5AH, Northern Ireland. E-mail: c.armstrong@qub.ac.uk     

Thermodynamic properties of the BaO-MnO flux system

Although a great number of works on BaO-bearing fluxes for refining Fe-Cr and Fe-Mn alloys have been carried out, there still remain several unresolved problems on using them in the refining process. The principal aim of the present study is to understand the thermodynamic properties of the BaO-MnO system, which has been shown to be very effective for dephosphorization of Fe-Mn alloys. The activity of manganese oxide in the BaO-MnO flux was measured at 1573 and 1673 K by equilibrating the flux, a Ag-Mn alloy, and a gas mixture of CO and CO₂ as functions of the flux composition and temperature. The influence of BaF₂, which is an effective additive for lowering the melting temperature of the flux, on the thermodynamics of the BaO-MnO system, including the solubility of MnO in the BaO-BaF₂ system, was also investigated.     

Characterization of poly(L-lactide)-block-poly(ethylene oxide)-block-poly(L-lactide) triblock copolymer by liquid chromatography at the critical condition and by MALDI-TOF mass spectrometry

Poly(L-lactide)-block-poly(ethylene oxide)-block-poly(L-lactide) triblock copolymers (PLLA-b-PEO-b-PLLA) were fractionated in terms of the number of LLA units by liquid chromatography at the critical condition (LCCC) of PEO block. The fractionated samples were identified using MALDI-TOF mass spectrometry. The dependence of the LCCC retention of the diblock and triblock copolymers on the degree of polymerization of PLLA block(s) follows Martin's rule very well. Unlike the case of PEO-b-PLLA diblock copolymer reported earlier (Lee, H.; et al. Macromolecules 1999, 32, 4143), however, a splitting of the elution peaks containing the same number of LLA units was found. The peak splitting was ascribed to the different length distributions of PLLA blocks at the two ends of the PEO block. From the relative intensities of the peaks, the split peaks were assigned to different isomeric structures of the PLLA blocks. From these results we conclude that the interaction of the triblock copolymers with the stationary phase is affected by the distribution of the interacting blocks at the two ends of the center PEO block, in addition to the total number of LLA units in the triblock copolymer.     

Effect of MDA-endcapped CTBN on the cure kinetics of epoxy system by autocatalytic cure rate expression

The cure rate of diglycidyl ether of bisphenol A (DGEBA)/4,4-methylene dianiline (MDA) system with or without MDA-endcapped carboxyl-terminated butadiene acrylonitrile (CTBN) rubber was studied by autocatalytic cure rate expression. All the cumulative conversion curves for DGEBA/MDA system with or without MDA-endcapped CTBN (20 phr) showed s-shape and this meant that the two systems followed the typical autocatalytic reaction. The cure rate of the system with MDA-endcapped CTBN (20 phr) was faster than that of the system without MDA-endcapped CTBN (20 phr). The activation energies of k ₁ and k ₂ for DGEBA/MDA system were 54.01 kJ/mol and 44.06 kJ/mol, respectively and those of k ₁ and k ₂ for the system with MDA-endcapped CTBN (20 phr) were 47.71 kJ/mol and 40.95 kJ/mol.