Time- and space-resolved spectroscopy of dynamic hohlraum interiors

A dynamic hohlraum is created when an annular z-pinch plasma implodes onto a cylindrical 0.014 g/cc 6-mm-diameter CH₂ foam. The impact launches a radiating shock that propagates toward the axis at 350 μm/ns. The radiation trapped by the tungsten z-pinch plasma forms a 200 eV hohlraum that provides X-rays for indirect drive inertial confinement fusion capsule implosion experiments. We are developing the ability to diagnose the hohlraum interior using emission and absorption spectroscopy of Si atoms added as a tracer to the central portion of the foam. Time- and space-resolved Si spectra are recorded with an elliptical crystal spectrometer viewing the cylindrical hohlraum end-on. A rectangular aperture at the end of the hohlraum restricts the field of view so that the 1D spectrometer resolution corresponds approximately to the hohlraum radial direction. This enables distinguishing between spectra from the unshocked radiation-heated foam and from the shocked foam. Typical spectral lines observed include the Si Lyα with its He-like satellites and the He-like resonance sequence including Heα, Heβ, and Heγ, along with some of their associated Li-like satellites. Work is in progress to infer the hohlraum conditions using collisional–radiative modeling that accounts for the radiation environment and includes both opacity effects and detailed Stark broadening calculations. These 6-mm-scale radiation-heated plasmas might eventually also prove suitable for testing Stark broadening line profile calculations or for opacity measurements.     

Optimization of silica silanization by 3-aminopropyltriethoxysilane

Thin films of 3-aminopropyltriethoxysilane (APTES) are commonly used to promote adhesion between silica substrates and organic or metallic materials with applications ranging from advanced composites to biomolecular lab-on-a-chip. Unfortunately, there is confusion as to which reaction conditions will result in consistently aminated surfaces. A wide range of conflicting experimental methods are used with researchers often assuming the creation of smooth self-assembled monolayers. A range of film morphologies based on the film deposition conditions are presented here to establish an optimized method of APTES film formation. The effect of reaction temperature, solution concentration, and reaction time on the structure and morphology was studied for the system of APTES on silica. Three basic morphologies were observed: smooth thin film, smooth thick film, and roughened thick film.     

Diverse redox-active molecules bearing identical thiol-terminated tripodal tethers for studies of molecular information storage

To examine the effects of molecular structure on charge storage in self-assembled monolayers (SAMs), a family of redox-active molecules has been prepared wherein each molecule bears a tether composed of a tripodal linker with three protected thiol groups for surface attachment. The redox-active molecules include ferrocene, zinc porphyrin, ferrocene-zinc porphyrin, magnesium phthalocyanine, and triple-decker lanthanide sandwich coordination compounds. The tripodal tether is based on a tris[4-(S-acetylthiomethyl)phenyl]-derivatized methane. Each redox-active unit is linked to the methane vertex by a 4,4'-diphenylethyne unit. The electrochemical characteristics of each compound were examined in solution and in SAMs on Au. Redox-kinetic measurements were also performed on the SAMs (with the exception of the magnesium phthalocyanine) to probe (1) the rate of electron transfer in the presence of an applied potential and (2) the rate of charge dissipation after the applied potential is disconnected. The electrochemical studies of the SAMs indicate that the tripodal tether provides a more robust anchor to the Au surface than does a tether with a single site of attachment. However, the electron-transfer and charge-dissipation characteristics of the two tethers are generally similar. These results suggest that the tripodal tether offers superior stability characteristics without sacrificing electrochemical performance.     

Controlled Dispersion and Setting of Cellulose Nanofibril - Carboxymethyl Cellulose Pastes

Cellulose - This work investigated the redispersion and setting behavior of highly loaded (~?18 wt.% solids in water) pastes of cellulose nanofibrils (CNFs) with carboxymethyl cellulose...     

Mechanical enhancement of cellulose nanofibril (CNF) films through the addition of water-soluble polymers

Cellulose - In this work, water-soluble polymers were screened through solution casting and polyvinyl alcohol (PVA) and poly(2-ethyl-2-oxazoline) (PEOX) were found as reinforcement agents for...     

Vocal Parameters of Aerobic Instructors with and without Voice Problems

Aerobic instructors frequently experience vocal fatigue and are at risk for the development of vocal fold pathology. Six female aerobic instructors, three with self-reported voice problems and three without, served as subjects. Measures of vocal function (perturbation and EGG) were obtained before and after a 30-minute exercise session. Results showed that the group with self-reported voice problems had greater amounts of jitter, lower harmonic-to-noise ratios, and less periodicity in sustained vowels overall, but no significant differences in measures of perturbation and EGG were found before and immediately after instruction. Measures of vocal parameters showed that subjects with self-reported voice problems projected with relatively greater vocal intensity and phonated for a greater percentage of time across beginning, middle, and ending periods of aerobic instruction than subjects with no reported voice problems.     

The Best Mixing Time for Random Walks on Trees

We characterize the extremal structures for mixing walks on trees that start from the most advantageous vertex. Let \(G=(V,E)\) be a tree with stationary distribution \(\pi \). For a vertex \(v \in V\), let \(H(v,\pi )\) denote the expected length of an optimal stopping rule from v to \(\pi \). The best mixing time for G is \(\min _{v \in V} H(v,\pi )\). We show that among all trees with \(|V|=n\), the best mixing time is minimized uniquely by the star. For even n, the best mixing time is maximized by the uniquely path. Surprising, for odd n, the best mixing time is maximized uniquely by a path of length \(n-1\) with a single leaf adjacent to one central vertex.     

Optimized mechanical and impact performance of high strength tempo oxidized cellulose nanofibril (TOCNF)—epoxy laminates

Cellulose - In this work, TEMPO cellulose nanofibril (TOCNF) laminates were fabricated using a layup method. Two different TOCNF layers were tested, a neat TOCNF and a TOCNF with polyvinyl alcohol...     

Triple-decker sandwich compounds bearing compact triallyl tripods for molecular information storage applications

The design of redox-active molecules that afford multistate operation and high charge density is essential for molecular information storage applications. Triple-decker sandwich compounds composed of two lanthanide metal ions and three porphyrinic ligands exhibit a large number of oxidation states within a relatively narrow electrochemical window. High charge density requires a small footprint upon tethering triple deckers to an electroactive surface. All triple deckers examined to date for information storage have been tethered via the terminal ligand and have exhibited large footprints (approximately 670 A2). Five new homonuclear (Eu or Ce) triple deckers have been prepared (via statistical or rational methods) to examine the effect of tether attachment site on molecular footprint. Three triple deckers are tethered via the terminal ligand (porphyrin) or central ligand (porphyrin or imidazophthalocyanine), whereas two triple deckers each bear two tethers, one at each terminal ligand. The tether is a compact triallyl tripod. Monolayers of the triple deckers on Si(100) were examined by electrochemical and FTIR techniques. Each triple decker exhibited the expected four resolved voltammetric waves, owing to formation of the mono-, di-, tri-, and tetracations. The electrochemical studies of surface coverage (gamma, obtained by integrating the voltammetric waves) reveal that coverages approaching 10(-10) mol cm(-2), corresponding to a molecular footprint of approximately 170 A2, are readily achieved for all five of the triple deckers. The surface coverage observed for the tripodal functionalized triple deckers is approximately 4-fold higher than that obtained for monopodal-functionalized triple deckers (carbon, oxygen, or sulfur anchor atoms) attached to either Si(100) or Au(111). The fact that similar, relatively high, surface coverages can be achieved regardless of the location (or number) of the tripodal tether indicates that the tripodal functionalization, rather than the location of the tether, is the primary determinant of the packing density.