A new criterion for the glass-forming ability of liquids

Based on theoretical calculations using the fragility concept and the nucleation theory for a model glass-forming system, we propose a dimensionless criterion, ?, expressed by T_rg(ΔT_x/T_g)^a, with T_rg, the reduced glass-transition temperature, ΔT_x, the width of the supercooled liquid region when heating a glass, T_g, the glass transition temperature, and a, the exponent. The application of this simple criterion to various glasses, including network, metallic, and molecular glasses (except pure water), indicates an excellent correlation between the critical cooling rate R_c and ? in a Log R_c-? single master plot with a = 0.143.     

Photoinitiator-Free Photopolymerization of Silicon-Containing Maleimides Based on Electron-Donor-Acceptor Systems

Summary: Photocured coatings promise enhanced performance, higher productivity and an improved environmental impact on the favorable reduction or near elimination of volatile organic compounds. Increasing interest in the photocuring industry has been imposed on the “photoinitiator-free photopolymerization [PIFP]” system based on the electron-donor-acceptor [EDA] concept, which commonly employs a mixture of a vinyl ether monomer (donor) and an N-substituted maleimide or bismaleimide monomer (acceptor). The PIFP systems employing silicon-containing maleimides together with vinyl ether monomers were firstly investigated and their photoreactions resulted in quite fast curing comparable to the conventional acrylate- based photocurable systems.     

Use of SDS micelles to stabilize a ternary intermediate in the reaction of ferrioxamine B and 1,10-phenanthroline

Spectrophotometric measurements of the reaction of ferrioxamine B (FeHDFB(+)) with 1,10-phenanthroline (phen) reveal the presence of a ternary intermediate complex in both aqueous solution and an aqueous solution of 0.16 M sodium dodecyl sulfate (SDS). The stoichiometry of the intermediate is Fe(H(2)DFB)(phen)(2+) on the basis of a Schwarzenbach analysis of spectrophotometric data obtained at variable pH and phen concentrations. The ternary complex formation constant for the reaction FeHDFB(+) + H(+) + phen right arrow over left arrow Fe(H(2)DFB)(phen)(2+) is log K = 6.96 in aqueous solution and log K = 8.64 in aqueous 0.16 M SDS. The enhanced stability of Fe(H(2)DFB)(phen)(2+) in micellar solution was analyzed in terms of the pseudophase ion-exchange (PPIE) model of micellar reactions. The association constants for the binding of each reactant to the micellar pseudophase were measured by ultrafiltration. According to PPIE model calculations, the enhanced stability of Fe(H(2)DFB)(phen)(2+) in micellar SDS arises from a proximity effect created by the high local concentrations of reactants in the micellar pseudophase. The calculations also indicate that an inhibitory medium or compartmentalization effect is operative since the observed micellar enhancement is much smaller than predicted by the PPIE model. The micellar stabilization of the Fe(H(2)DFB)(phen)(2+) intermediate and the overall conversion of FeHDFB(+) to Fe(phen)(3)(2+) are discussed as a possible model system for siderophore iron release in microbial organisms.     

Fast and sensitive DNA analysis using changes in the FRET signals of molecular beacons in a PDMS microfluidic channel

A new DNA hybridization analytical method using a microfluidic channel and a molecular beacon-based probe (MB-probe) is described. A stem-loop DNA oligonucleotide labeled with two fluorophores at the 5′ and 3′ termini (a donor dye, TET, and an acceptor dye, TAMRA, respectively) was used to carry out a fast and sensitive DNA analysis. The MB-probe utilized the specificity and selectivity of the DNA hairpin-type probe DNA to detect a specific target DNA of interest. The quenching of the fluorescence resonance energy transfer (FRET) signal between the two fluorophores, caused by the sequence-specific hybridization of the MB-probe and the target DNA, was used to detect a DNA hybridization reaction in a poly(dimethylsiloxane) (PDMS) microfluidic channel. The azoospermia gene, DYS 209, was used as the target DNA to demonstrate the applicability of the method. A simple syringe pumping system was used for quick and accurate analysis. The laminar flow along the channel could be easily controlled by the 3-D channel structure and flow speed. By injecting the MB-probe and target DNA solutions into a zigzag-shaped PDMS microfluidic channel, it was possible to detect their sequence-specific hybridization. Surface-enhanced Raman spectroscopy (SERS) was also used to provide complementary evidence of the DNA hybridization. Our data show that this technique is a promising real-time detection method for label-free DNA targets in the solution phase. Figure FRET-based DNA hybridization detection using a molecular beacon in a zigzag-shaped PDMS microfluidic channel     

Immobilization of aminophenylboronic acid on magnetic beads for the direct determination of glycoproteins by matrix assisted laser desorption ionization mass spectrometry

Aminophenylboronic acid (APBA) has been immobilized on magnetic beads for the direct determination of glycoprotein by matrix assisted laser desorption/ionizaton time of flight mass spectrometry (MALDI-TOF-MS). An APBA layer was formed on the surface of carboxylic acid terminated magnetic beads by coupling with carbodiimide and subsequently reacted with an N-hydroxysuccinimide moiety. The immobilized APBA was identified by MALDI-TOF-MS without a matrix. Glycoproteins, such as HbA1c, fibrinogen, or RNase B were separated and desalted using APBA magnetic beads by simply washing the magnetic beads and then separating them by external magnet. Proteins can be identified by direct determination of proteins on beads on MALDI plate and confirmed again by peptide mass finger printing after digestion of proteins on magnetic beads by trypsin. Fluorescence image with a FITC tagging protein using confocal laser microscopy showed the difference of immobilization efficiency between glycoproteins and nonglycoproteins. The methods developed within this work allow the simple treatment and enrichment of glycoproteins as well as direct determination of proteins on beads by MALDI-TOF-MS.     

Properties of as-cast and structurally relaxed Zr-based bulk metallic glasses

We have studied the influence of the arc melting procedure of Nb-containing Zr-based bulk metallic glasses (BMGs) on their thermal and mechanical properties. We found that the strength and plastic strain to failure, determined at room temperature, increases by the addition of a few percentage of Nb into the Zr-based BMGs. High-resolution transmission-electron microscopy results show that the addition of 2 at.% Nb introduces the formation of as-cast nanocrystals. At the same time, thermal analyses indicate an increase in glass forming ability with the small addition of Nb. Contrary to the reported results in other amorphous alloys, we found that the plastic strain increases further after heat-induced structural relaxation in the Zr-based BMGs.     

Bicriteria linear fractional programming

As a step toward the investigation of the multicriteria linear fractional program, this paper provides a thorough analysis of the bicriteria case. It is shown that the set of efficient points is a finite union of linearly constrained sets and the efficient frontier is the image of a finite number of connected line segments of efficient points. A simple algorithm using only one-dimensional parametric linear programming techniques is developed to evaluate the efficient frontier.This research was partially supported by NRC Research Grant No. A4743. The authors wish to thank two anonymous referees for their helpful comments on an earlier draft of this paper.     

High work function of Al-doped zinc-oxide thin films as transparent conductive anodes in organic light-emitting devices

Deposition of Al-doped ZnO (AZO) films with various film thicknesses on glass substrates was performed to investigate the feasibility of using AZO films as anode electrodes in organic light-emitting devices (OLEDs). The electrical resistivity of the AZO films with a 180-nm thickness was 4.085 × 10⁻² Ω cm, and the average optical transmittance in the visible range was 80.2%. The surface work function for the AZO films, determined from the secondary electron emission coefficients obtained with a focused ion beam, was as high as 4.62 eV. These results indicate that AZO films grown on glass substrates hold promise for potential applications as anode electrodes in high-efficiency OLEDs.     

Effective barrier height and work function of Mg:Ag thin films with a low Mg concentration acting as cathodes in high-efficiency organic light emitting devices

Organic molecular-beam deposition (OMBD) of Mg:Ag thin films with a low Mg concentration on tris(8-hydroxyquinolino) aluminum (Alq₃) layers at room temperature was performed to investigate the feasibility of using Mg:Ag thin films as cathode electrodes in organic light-emitting devices (OLEDs). The effective barrier height of the Mg:Ag (5:95) thin films grown on the Alq₃ layers, determined from the current-voltage measurements, was as low as 0.22 eV. The work function of the Mg:Ag (5:95) thin film, determined from the secondary electron emission coefficients obtained by using focused ion beam, was 4.12 eV. These results indicate that Mg:Ag (5:95) thin films with a low Mg concentration grown by using the OMBD method hold promise for potential applications as cathode electrodes in high-efficiency OLEDs.