Since the discovery of surfactant-templated silica by Mobil scientists in 1992, mesostructured silica has been synthesized in various forms including thin films, powders, particles, and fibers. In general, mesostructured silica has potential applications, such as in separation, catalysis, sensors, and fluidic microsystems. In respect to these potential applications, mesostructured silica in the form of thin films is perhaps one of the most promising candidates. The preparation of mesostructured silica films through preferential solvent evaporation-induced self-assembly (EISA) has recently received much attention in the laboratories. However, no amphiphile/silica films with reverse mesophases have ever been made through this EISA procedure. Furthermore, templates employed to date have been either surfactants or poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) triblock copolymers, such as pluronic P-123, both of which are water-soluble and alcohol-soluble. Due to their relatively low molecular weight, the templated silica films with mesoscopic order have been limited to relatively small characteristic length scales. In the present communication, the authors report a novel synthetic method to prepare mesostructured amphiphilic/silica films with regular and reverse mesophases of large characteristic length scales. This method involves evaporation-induced self-assembly (EISA) of amphiphilic polystyrene-block-poly(ethylene oxide) (PS-b-PEO) diblock copolymers. In the present study, the PS-b-PEO diblocks are denoted as, for example, …

The U(l) triangle anomaly is present, as an infra-red divergence, in the six-reggeon triple-regge interaction vertex obtained from a maximally non-planar Feynman diagram in the full triple-regge limit of three-to-three quark scattering.

The TEAM Workshops originated from problems in fusion research. Based on recent observations regarding automotive modeling, the author asks whether TEAM-like workshops, and the accompanying cooperation among modelers, are of value in areas of economic competition.

The coupled-flow phenomenon, electro-osmosis, whereby water flow results from an applied electrical potential gradient, is being used at Lawrence Livermore National Laboratory to induce water flow through deep (25-40 meters below surface) fine-grained sediments. The scoping work described here lays the groundwork for implementation of this technology to remediate solvent-contaminated clayey zones at the LLNL site. The electro-osmotic conductivity (k{sub e}) measured in-situ between two 37 m deep wells, 3 m apart of 2.3 x 10{sup -9} m{sup 2}/s-V is in good agreement with the value determined from bench-top studies on the core extracted from one of the wells of 0.94 {+-} 0.29 x 10{sup -9} m{sup 2}/s-V. Hydraulic conductivity (k{sub h}) of the same core is measured to be 2.03 {+-} 0.36 x 10{sup -10} m/s. Thus, a voltage gradient of 1 V/cm produces an effective hydraulic conductivity of {approx}1 x 10{sup -7} m/s; an increase in conductivity of nearly three orders of magnitude.

The workshop is divided into the following subjects: water quality, air quality, biological impact, hazards, environmental impact evaluation, and land use and socio-economic impact. Individual problems in each subject area are evaluated by the following criteria: probability of occurrence, seriousness of consequences, resource applicability, time urgency for new research, and researchability for new research. Recommended approaches to solution are given for each problem. Minority statements are given in some cases. (MHR)

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Ge nanocrystals are formed in silica by ion beam synthesis and are subsequently exposed by selective HF etching of the silica. Under ambient conditions, the exposed nanocrystals are stable after formation of a protective native oxide shell of no more than a few monolayers. However, under visible laser illumination at room temperature and in the presence of O{sub 2}, the nanocrystals rapidly oxidize. The oxidation rate was monitored by measuring the Raman spectra of the Ge nanocrystals in-situ. The intensity ratio of the anti-Stokes to the Stokes line indicated that no significant laser-induced heating of illuminated nanocrystals occurs. Therefore, the oxidation reaction rate enhancement is due to a photo-chemical process. The oxidation rate varies nearly linearly with the logarithm of the laser intensity, and at constant laser intensity the rate increases with increasing photon energy. These kinetic measurements, along with the power dependencies, are described quantitatively by an electron active oxidation mechanism involving tunneling of optically excited electrons through the forming oxide skin and subsequent transport of oxygen ions to the Ge nanocrystal surface.