Ciliation and lamellae in crystalline polymers

Molecular cilia, the uncrystallized portions of chains already partly attached to polymer crystals, exert a profound influence on the course of polymeric crystallization with ultimate responsibility for the divergence of adjacent lamellae which leads to spherulitic growth. Their effective size and pressure have been measured, in α-polypropylene, from electron microscopic measurements of the separation and maximum curvature of lamellae in row structures. That cilia exist and extend the effective region occupied by a lamella beyond the geometrical confines of its fold surfaces is important for crystallization theory and may well have implications for the connection of lamellae into networks and for gelation.     

A computational study of x-ray emission from high-Z x-ray sources on the National Ignition Facility laser

We have begun to use 350–500 kJ of 1/3-micron laser light from the National Ignition Facility (NIF) laser to create millimeter-scale, bright multi-keV x-ray sources. In the first set of shots we achieved 15%–18% x-ray conversion efficiency into Xe M-shell (∼1.5–2.5 keV), Ar K-shell (∼3 keV) and Xe L-shell (∼4–5.5 keV) emission (Fournier et al., Phys. Plasmas 17, 082701, 2010), in good agreement with the emission modeled using a 2D radiation-hydrodynamics code incorporating a modern Detailed Configuration Accounting atomic model in non-LTE (Colvin et al., Phys. Plasmas, 17, 073111, 2010). In this paper we first briefly review details of the computational model and comparisons of the simulations with the Ar/Xe NIF data. We then discuss a computational study showing sensitivity of the x-ray emission to various beam illumination details (beam configuration, pointing, peak power, pulse shape, etc.) and target parameters (size, initial density, etc.), and finally make some predictions of how the x-ray conversion efficiency expected from NIF shots scales with atomic number of the emitting plasma.     

Stability of nitrogen-oxygen cages N12O2, N14O2, N14O3, and N16O4

Molecules consisting entirely of nitrogen have been studied extensively for their potential as high energy density materials (HEDM). However, many such molecules are too unstable to serve as practical energy sources. This has prompted many studies of molecules that are mostly nitrogen but which incorporate heteroatoms into the structure to provide additional stability. In the current study, cages of three-coordinate nitrogen are viewed as candidates for stabilization by insertion of oxygen atoms into the nitrogen framework. Cages of N12, N14, and N16 with four-membered rings are studied because four-membered rings have been previously shown to be a destabilizing influence. Insertion of oxygen atoms, which converts N-N bonds to N-O-N bonding groups, relieves ring strain and can potentially result in stable molecules. These molecules are studied by theoretical calculations, using Hartree-Fock and Moller-Plesset (MP3 and MP4) theories, to determine the dissociation energies of the molecules. The primary result of the study is that stable molecules can result from oxygen insertion but that oxygen-oxygen proximity destabilizes the insertion products.     

Interlaboratory comparison of size and surface charge measurements on nanoparticles prior to biological impact assessment

The International Alliance for NanoEHS Harmonization (IANH) organises interlaboratory comparisons of methods used to study the potential biological impacts of nanomaterials. The aim of IANH is to identify and reduce or remove sources of variability and irreproducibility in existing protocols. Here, we present results of the first IANH round robin studies into methods to assess the size and surface charge of suspended nanoparticles. The test materials used (suspensions of gold, silica, polystyrene, and ceria nanoparticles, with [primary] particles sizes between 10?nm and 80?nm) were first analysed in repeatability conditions to assess the possible contribution of between-sample heterogeneity to the between-laboratory variability. Reproducibility of the selected methods was investigated in an interlaboratory comparison between ten different laboratories in the USA and Europe. Robust statistical analysis was used to evaluate within- and between-laboratory variability. It is shown that, if detailed shipping, measurement, and reporting protocols are followed, measurement of the hydrodynamic particle diameter of nanoparticles in predispersed monomodal suspensions using the dynamic light scattering method is reproducible. On the other hand, measurements of more polydisperse suspensions of nanoparticle aggregates or agglomerates were not reproducible between laboratories. Ultrasonication, which is commonly used to prepare dispersions before cell exposures, was observed to further increase variability. The variability of the zeta potential values, which were also measured, indicates the need to define better surface charge test protocols and to identify sources of variability.     

Do intelligent configuration search techniques outperform random search for large molecules?

We compare three global configuration search methods on a scalable model problem to measure relative performance over a range of molecule sizes. Our model problem is a 2-D polymer composed of atoms connected by rigid rods in which all pairs of atoms interact via Lennard–Jones potentials. The global minimum energy can be calculated analytically. The search methods are all hybrids combining a global sampling algorithm with a local refinement technique. The sampling methods are simulated annealing (SA ), genetic algorithms (GA ), and random search. Each of these uses a conjugate gradient (CG ) routine to perform the local refinement. Both GA and SA perform progressively better relative to random search as the molecule size increases. We also test two other local refinement techniques in addition to CG , coupled to random search as the global method. These are simplex followed by CG and simplex followed by block-truncated Newton. For small problems, the addition of the intermediate simplex step improved the performance of the overall hybrid method. © 1992 John Wiley & Sons, Inc.     

PbSe/CdSe and PbSe/CdSe/ZnSe hierarchical nanocrystals and their photoluminescence

Multiple CdSe and ZnSe semiconductor shells were grown on PbSe semiconductor spherical cores with monolayer control. For CdSe shell coating, we found that there was little room to further increase the quantum yields of freshly-made high-quality PbSe nanocrystals that already owned very high initial values because of their good surface status; but there was great improvement for the PbSe nanocrystals with low initial quantum yields because of the poor surface status. Nonetheless, the quantum yield for the latter case could not reach the former's value. Additional ZnSe shells on PbSe/CdSe could further increase the quantum yield and protect the nanocrystals from air oxidation. The observed phenomena in the synthesis of the PbSe/CdSe and PbSe/CdSe/ZnSe core/shell structures were explained through the carrier wave function expansion and the surface polarization.     

Mechanism of transition between cellulose I and cellulose II during mercerization

It is suggested that the transformation from cellulose I to cellulose II during mercerization is the result of a progressive shift of the sheets of cellulose chains within the crystallites of a microfibril from the quarter-staggered relation in cellulose I to complete correspondence in cellulose II. Qualitatively, the results of such a shift would be consistent with the observed increases in lateral disorder, changes in cell dimensions, swelling, changes in infrared absorption, increases in reactivity of hydroxyl groups and especially with changes in the relative intensities of meridional, x-ray diffraction reflections of cellulose fibers. The consequences of such a shift also include variations of the dihedral angle at the glycosidic linkage to provide an opportunity for the conformational changes which have been deduced from Raman and infrared spectra. Such a shift may take place in the transformation of native celluloses with antiparallel structure as well as those with parallel polarity. It is consistent with and is able to explain examples of “memory” of previous treatment in cellulose samples.     

When might silylenes behave more like carbenes? : Sihli,a triplet silylene

Qualitative arguments and preliminary theoretical studies by Harrison suggest that lithiosilylene (SiHLi) may have a triplet electronic ground state. This possibility has been confirmed in the present detailed ab initio quantum mechanical study. Using double-zeta and double-zeta plus polarization basis sets, the different low-lying electronic states of SiHLi have been investigated using self-consistent-field and configuration interaction methods. The triplet ground state potential surface is very flat, with two nearly degenerate minima at θ (HSiLi) values of 137° and 48°, respectively. The lowest singlet state lies ~ 7 kcal higher in energy and is predicted to have an equilibrium bond angle of ~93°, much like the parent silylene SiH₂. Vibrational frequencies are predicted for all stationary points.