Adsorption of cationic monomeric and gemini surfactants on montmorillonite and adsolubilization of vitamin E

Adsorption of a cationic gemini surfactant (1,2-bis(dodecyldimethylammonio) ethane dibromide, 12-2-12) and the corresponding monomeric surfactant (dodecyltrimethylammonium bromide, DTAB) on montmorillonite has been characterized with a combination of adsorption isotherm, interlayer spacing and FT-IR spectroscopic data. Adsolubilization of vitamin E into the adsorbed surfactant layers has also been studied. The adsorption isotherm data reveal that the adsorption of the two surfactants is driven by the two factors: one is the cation exchange that occurs on the interlayer basal planes and the other is the hydrophobic interaction between hydrocarbon chains of the surfactants. Although the adsorbed amount measured in the saturation region (in mol g(-1)) is almost identical for the two surfactants, the conformation of the intercalated surfactant molecules differs significantly from each other. The adsorption of DTAB results in a lateral bilayer arrangement in the limited interlayer space, whereas 12-2-12 gives a normal bilayer arrangement in the expanded interlayer space. Adsolubilization of vitamin E takes place into the adsorbed surfactant layers, and interestingly, all the vitamin E molecules added in the montmorillonite suspensions are hybridized at lower surfactant concentrations due to the great specific surface area of the clay material. Since the maximum adsolubilization amount is usually obtained just below the critical micelle concentration, the gemini surfactant is deemed to be more efficient than the corresponding monomeric one to achieve the great adsolubilization amount.     

Tradeoffs in granularity and parallelization for a Monte Carlo shower simulation code

The EGS4 code, developed at Stanford Linear Accelerator Center, simulates electron-photon cascading phenomena. The original code is inherently sequential: processing one particle at a time. This paper reports on a series of experiments in parallelizing different versions of EGS4. Our parallel experiments were run on a 30-processor Sequent Balance B21 and a 6-processor Symmetry S27. We have considered the following approaches for parallel execution of this application code:

1. (1) Original sequential version modified for parallel processing: 1 processor;

2. (2) Version 1 run multiprocessed: 1 to 29 processors;

3. (3) Sequential version modified for large-grain parallel processing: 1 procssor;

4. (4) Version 3 run using the Sequent Microtasking Library: 1 to 29 processors.

For each approach, we discuss the relative advantages and disadvantages in the areas of coding effort, understandability and portability, as well as performance, and outline a new parallelization approach we are currently pursuing based on Large-Grain Data Flow techniques.     

Viscoelastic behavior of poly(butyl methacrylate) densely grafted on silica nanoparticles

A series of poly(butyl methacrylate)s (PBMAs) with various molar masses (33 000–270 000 g mol^?1), which were densely grafted on fumed silica nanoparticles (PBMA–SiO₂), were synthesized by surface‐initiated atom transfer radical polymerization. The dynamic viscoelastic behavior of PBMA–SiO₂ was systematically investigated in the solid and molten states with oscillatory strains, and compared to that of a conventional nanocomposite (PBMA/SiO₂). The storage moduli of PBMA–SiO₂ and PBMA/SiO₂ are equivalent in the solid state, whereas the storage modulus of PBMA–SiO₂ is lower than that of PBMA/SiO₂ in the molten state, especially at high silica loading. This is because the formation of a network structure composed of the silica nanoparticles in PBMA–SiO₂ is strongly suppressed by the polymer brushes on the particles. In contrast, even at low silica loading, the PBMA–SiO₂ system exhibits a gel‐like behavior resulting from a steric repulsion between the composite particles, because all of the tethered polymers behave as bound polymers. Copyright © 2011 Society of Chemical Industry     

Enzymatic enrichment of arachidonic acid from Mortierella single-cell oil

An attempt was made to enrich arachidonic acid (AA) from Mortierella single-cell oil, which had an AA content of 25%. The first step involved the hydrolysis of the oil with Pseudomonas sp. lipase. A mixture of 2.5 g oil, 2.5 g water, and 4000 units (U) Pseudomonas lipase was incubated at 40°C for 40 h with stirring at 500 rpm. The hydrolysis was 90% complete after 40 h, and the resulting free fatty acids (FFA) were extracted with n-hexane (AA content, 25%; recovery of AA, 91%). The second step involved the selective esterification of the fatty acids with lauryl alcohol and Candida rugosa lipase. A mixture of 3.5 g fatty acids/lauryl alcohol (1:1, mol/mol), 1.5 g water, and 1000 U Candida lipase was incubated at 30°C for 16 h with stirring at 500 rpm. Under these conditions, 55% of the fatty acids were esterified, and the AA content in the FFA fraction was raised to 51% with a 92% yield. The long-chain saturated fatty acids in the FFA fraction were eliminated as urea adducts. This procedure raised the AA content to 63%. To further elevate the AA content, the fatty acids were esterified again in the same manner with Candida lipase. The repeated esterification raised the AA content to 75% with a recovery of 71% of its initial content.     

Influence of heating and laser irradiation on the Raman D band in single-wall carbon nanotubes

Fine structure of the Raman D band in single-wall carbon nanotubes (SWNTs) was investigated by heating and laser irradiation. It is shown that the D band is composed of three components at ～ 1313, 1340, and 1355 cm^? 1, denoted by D₁, D₂, and D₃, respectively. The D₁ and D₂ intensities significantly increase with laser irradiation in air and vacuum, respectively. The D₃ intensity drastically increases with heating in air. From these results, it is suggested that the fine structure of the D band is attributed to different kinds of defects introduced in SWNTs.     

Dielectric properties of Permalloy granular composite materials

Dielectric and electrical properties of Permalloy granular composite materials have been studied considering the application to left-handed meta-materials. Surface oxidized Permalloy particles have high surface electrical resistance; the eddy current effect in the composite structure is suppressed. The electrical conductivity of compacted Permalloy particles increases with increasing temperature and indicates the semiconductive layer formation on the particle. The low frequency ac electrical conductivity of Permalloy composite materials shows a drastic increase in the particle content between 50 and 60 vol.%. Electrical permittivity spectra of Permalloy composites show a non-metallic characteristic and the enhancement of permittivity is observed with increase of Permalloy particle content.     

Vortex Generation in Cyclically Coupled Superfluids and the Kibble-Zurek Mechanism

We study theoretically the generation of cyclic supercurrent among three superfluids coupled by the Josephson Junctions. Depending on the initial relative phases between superfluids, Josephson current flows cyclically through the superfluids to create a quantized vortex. Reducing the coupling strength changes the motion from periodic to chaotic, thus suppressing the cyclic current. Applying this result to the Kibble-Zurek mechanism, the probability of the vortex generation via this mechanism is modified from the simple estimate given by the geodesic rule. We compare our results with the Lancaster, Grenoble and Helsinki experiments.     

Macroscopic Quantum Tunneling of Two-Component Bose-Einstein Condensates

We show theoretically the existence of the metastable state and study the decay through the macroscopic quantum tunneling in two-component Bose-Einstein condensates. The numerical analysis of the coupled Gross-Pitaevskii equations clarifies the metastable states whose configuration preserves or breaks the symmetry of the trapping potential, depending on the interspecies interaction and the particle number. We calculate the tunneling decay rate of the metastable state by using the collective coordinate approximation and the bounce technique. It is found that the macroscopic quantum tunneling is observable in a wide range of the particle number.     

Interactive multiple objective linear programming system implemented on a microcomputer

Linear programming is one of the most widely used Operations Research/Management Science techniques. Recently, multiple objective decision making has been well established as a practical approach to seek a satisfactory solution to a decision making problem. Much attention has been focused on a microcomputer as an economical management tool.

In this paper we propose an interactive goal attainment method using the eigenvector algorithm for solving a multiple objective linear programming problem interactively on microcomputers. In the software package Micro-LPS based on the method proposed, we design a conversational and user-friendly system in which the user commands are involved.     

Chiral alkylated poly(m-phenylene)s: Optical activity and thermal stability of helical structures

Chiral poly[4,6-bis(alkylthio)-1,3-phenylene-alt-2-methyl-1,3-phenylene] was synthesized from 1,3-dibromo-2,6-bis(3-dodecyl-2-methylthio)benzene and 2-methyl-1,3-phenylenebis(pinacol borate) as a precursor of chiral poly(thiaheterohelicene). Circular dichroism (CD) spectra that arise from the poly(1,3-phenylene) backbone inverted according to the chirality of the side chains, which indicated that a helical conformation of the polymer was induced by the interaction between the side chains. The CD intensity of the polymer increased in non-polar solvents such as hexane. The decrease in the molar CD intensity and the broadening of a fluorescence band at higher concentrations suggested that the aggregation of the polymer suppressed the formation of the helical structure. The conformational changes were monitored by the CD and the ¹H NMR spectra at different temperatures. In a good solvent such as dichloromethane, the CD intensity increased, and the ¹H NMR signal of benzene protons shifted to lower fields at low temperatures. In hexane, the CD spectra and the ¹H NMR signals were less dependent on temperatures, as a result of the strong interaction between the chiral alkyl chains in the polymer to freeze the helical conformation.