Curvature effect on nanometer-scale surface properties of phospholipid layers

Phospholipid bilayers were formed through liposome fusion on surfaces with different curvatures that were defined with silica spheres deposited on silicon water. Prior to the fusion, the surfaces became hydrophobic with octadecyltrimethoxysilane solution. Using atomic force microscope, surface forces were measured on dipalmitoylphosphatidylcholine (DPPC) layers and dioleoylphosphatidylcholine (DOPC) layers upon the curvature at 25°C. The short-range repulsions were higher at 20 and 100 nm curvatures than other curvatures for the DPPC layer, while they were lower for the DOPC layer. Since it was known that the forces are related to its low mechanical stability of the lipid layer, this opposite behavior was analyzed in terms of stability upon the curvature, which appears to be eventually determined by the correlation between the lipid molecule geometry and the surface curvature.     

Comparative study of pesticide multi-residue extraction in tobacco for gas chromatography-triple quadrupole mass spectrometry

Coacervates made of surfactant aggregates, namely aqueous and reverse micelles and vesicles, were firstly used as solvents in single-drop microextraction (SDME) and proposed for the extraction and concentration of chlorophenols prior to liquid chromatography. The formation of coacervate drops in the needle tip of conventional microsyringes depended on the type of intermolecular forces established between the surfactant headgroups making up the supramolecular aggregates; hydrogen bond interactions were strong enough to permit the formation of spherical drops. Stability of 1-50 microL coacervate drops was achieved by introducing the microsyringe needle tip in a PTFE rod, the end of which had been machined out with a heated flanging-tool to get circular flanges (diameters in the range 3.5-6 mm). The parameters affecting the efficiency of single-drop coacervative microextraction (SDCME) were investigated using vesicular coacervates as a solvent and 2-chlorophenol (CP), 2,4-dichlorophenol (DCP), 2,4,6-trichlorophenol (TCP) and pentachlorophenol (PCP) as model analytes. Coacervative microextraction dynamics fit to the general rate equation of liquid-liquid extraction. The effect of variables such as extraction time, drop volume, stirring rate, pH and temperature, on the extraction of chlorophenols was similar to that described for organic solvent drops. Electrolyte concentrations above 0.1 M caused drop instability. Under the optimum conditions, detection limits were in the range 0.1-0.3 microg L(-1). The relative standard deviation was between 4.3 and 5.6 at 20 microg L(-1) spiked level. The method was applied to the determination of the four chlorophenols in wastewater, superficial water from a reservoir and groundwater and the recoveries were in the range 79 and 106% at 5-20 microg L(-1) spiked level.     

Temperature effect on nanometer-scale physical properties of mixed phospholipid monolayers

Mixed dipalmitoylphosphatidylcholine (DPPC) and dioleoylphosphatidylcholine (DOPC) monolayers have been deposited on mica using Langmuir-Blodgett technique, as a model system for biomembranes. Nanometer-scale surface physical properties were quantitatively characterized with the gradual temperature change using the atomic force microscope. At 25 degrees C, tapping mode imaging revealed the clear phase-separation in the form of microscopic DPPC domain embedded in a DOPC matrix and the obvious step height between the higher DPPC phase and the lower DOPC phase. Surface force measurement made at 25 degrees C in contact mode showed significant contrasts in deformation elasticity, adhesion, and jump-to-surface. These physical property differences were kept below 40 degrees C, while they almost disappeared over 40 degrees C. In addition, the reversibility of the properties for the temperature change was also found.     

Thermodynamic determination of solvation potentials of various metal chlorides by (1,4-dioxane + water) mixtures through EMF measurements

The EMF data of different metal chlorides (2:1 electrolytes) were obtained by using a cell [M_X Hg|MCl₂ (m)|AgCl–Ag] at two temperatures. Stock solutions of metal chlorides (CoCl₂, CuCl₂ and ZnCl₂) were prepared by weight in 1,4-dioxane–aqueous mixtures. There was a significant change in the EMF values with change of metal chloride, its concentration and solvents composition. The standard electrode potential (E°) values of the above cell were calculated from the measured EMF of these mixtures. The standard thermodynamic functions (ΔG°, ΔH° and ΔS°) and respective transfer parameters of MCl₂ from water to 20, 45 and 70% dioxane–water mixtures were also evaluated. Equilibrium dissociation constants (K₁ and K₂) as well as the degrees of dissociation (α₁ and α₂) were obtained by iterative procedures. The data were analyzed in terms of solute–solvent interactions depending on standard and transfer thermodynamic parameters and mean activity coefficients (γ_±) of electrolytes.     

Removal of 10-nm contaminant particles from Si wafers using argon bullet particles

Removal of nanometer-sized contaminant particles (CPs) from substrates is essential to successful fabrication of nano scale devices. But the cleaning limit of various current technologies stay around 50 nm. Cryogenic aerosol beam has long been successfully employed to remove CPs down to 50 nm, and supersonic particle beam using particles smaller than 100 nm lowered the limit of cleaning down to 20 nm size. In this study, the particle beam technique that uses nanometer-sized bullet particles moving at supersonic velocity was improved, and successfully employed to remove contaminant particles as small as 10 nm. Ar nano-bullets of about 20–50 nm were generated by gas-phase nucleation, and growth in a supersonic nozzle: appropriate size and velocity of the nano-bullets were obtained by optimizing the Ar/He mixture fraction and nozzle contours. Cleaning efficiency >95% was attained. Nano-bullet velocity was found to be the most important parameter affecting removal of contaminant particles in the 10-nm size range.     

n-Type microcrystalline silicon oxide layer and its application to high-performance back reflectors in thin-film silicon solar cells

Light trapping is a key issue in improving the efficiency of thin-film Si solar cells, and using a back reflector material plays a critical role in improving a cell's light-trapping efficiency. In this study, we developed n-type microcrystalline silicon oxide (n-μc-SiO_x) films that are suitable for use as back reflectors in thin-film silicon solar cells. They exhibit a lower refractive index and lower absorption spectra, especially at long wavelengths of >700 nm, than conventional ZnO:Al materials, which are beneficial for this application. The n-μc-SiO_x films were prepared by the PECVD (plasma-enhanced chemical vapor deposition) method and applied to the fabrication of back reflectors in μc-Si:H solar cells. We also characterized the changes in cell performance with respect to the refractive index, conductivity, and thickness of the n-μc-SiO_x back reflectors. The novel back reflector boosts the total current density by up to 3.0% with the help of the enhanced long-wavelength response. It also improves open circuit voltage (V_oc) and fill factor (FF), which may be attributed to the reduced shunt current caused by the anisotropic electrical characteristics of the n-μc-SiO_x layer. Finally, we could achieve a conversion efficiency for the hydrogenated microcrystalline silicon (μc-Si:H) solar cells of up to 9.3% (V_oc: 0.501 V, J_sc: 27.4 mA/cm², FF: 0.68) using the n-μc-SiO_x back reflector.     

Effect of aminoglycoside on mechanical properties of zwitterionic phospholipid vesicles

The effect of the aminoglycoside (streptomycin) incorporation on the nanomechanical properties of pure dipalmitoylphosphatidylcholine (DPPC) vesicles was studied using atomic force microscope (AFM) on mica surface. The vesicles were prepared by extrusion and adsorbed on the mica surface. The forces, measured between an AFM tip and the vesicle, presented that the breakthrough of the tip into the vesicles occurred two times. Each breakthrough represented each penetration of the tip into each bilayer. Force data prior to the first breakthrough were fitted well with the Hertzian model to estimate Young's modulus and bending modulus of the vesicles. It was found that the Young's modulus and bending modulus were not varied with the incorporation of AGs (streptomycins) up to the 1:1 AG/DPPC vesicle system. This result may suggest that the AGs do not lead to the disruption of DPPC packing.     

Comparison of interfacial properties of electrodeposited single carbon fiber/epoxy composites using tensile and compressive fragmentation tests and acoustic emission

Interfacial and microfailure properties of carbon fiber/epoxy composites were evaluated using both tensile fragmentation and compressive Broutman tests with an aid of acoustic emission (AE). A monomeric and two polymeric coupling agents were applied via the electrodeposition (ED) and the dipping applications. A monomeric and a polymeric coupling agent showed significant and comparable improvements in interfacial shear strength (IFSS) compared to the untreated case under both tensile and compressive tests. Typical microfailure modes including cone-shaped fiber break, matrix cracking, and partial interlayer failure were observed under tension, whereas the diagonal slipped failure at both ends of the fractured fiber exhibited under compression. Adsorption and shear displacement mechanisms at the interface were described in terms of electrical attraction and primary and secondary bonding forces. For both the untreated and the treated cases AE distributions were separated well in tension, whereas AE distributions were rather closely overlapped in compression. It might be because of the difference in molecular failure energies and failure mechanisms between tension and compression. The maximum AE voltage for the waveform of either carbon or large-diameter basalt fiber breakages in tension exhibited much larger than that in compression. AE could provide more likely the quantitative information on the interfacial adhesion and microfailure.     

Determination of 1-deoxynojirimycin in Morus alba L. leaves by derivatization with 9-fluorenylmethyl chloroformate followed by reversed-phase high-performance liquid chromatography

A rapid and reliable method suitable for assays of a large number of Morus alba leaves for 1-deoxynojirimycin (DNJ) has been developed. DNJ in 0.1 g of freeze-dried leaves was double-extracted in 10 mL of aqueous 0.05 M HCl by vortexing for 15 s at room temperature, derivatized with 9-fluorenylmethyl chloroformate (FMOC-Cl), and analyzed by reversed-phase high-performance liquid chromatography (RP-HPLC) equipped with a fluorescence detector. The double extraction recovered > 99% of extractable DNJ from the leaves. Stabilization of FMOC-derivatized DNJ (DNJ-FMOC) was achieved by diluting the reactant with aqueous acetic acid after derivatization. DNJ-FMOC was stable for at least 16 days under acidic conditions at room temperature (24 degrees C). Linearity ranged between 0.3 and 30 microg mL(-1). The intra- and inter-day precision for DNJ-spiked biological samples was between 0.6 and 1.8% and between 3.7 and 4.5%, respectively.