Edge-effect studies in fiber-reinforced laminates

Experimental and theoretical studies of edge effects in rectangular composite strips under tension are discussed. The objective of the study was to investigate the effect of various parameters, including reinforcement material, fiber orientation and the structure of the reinforcement, on the various quantities which are observed in the vicinity of free edges in multidirectionally reinforced laminates. Of particular interest was the confirmation of theoretical results related to differences in response of graphite- and boron-reinforced laminates. Experiments consisted of moiré measurements of surface-displacement patterns which were compared with theoretical predictions, and examination of failure levels. The experiments were carried out on AVCO 5505 boron and Whitaker 5206 MODMOR II graphite-reinforced angle-ply laminates in which both stacking sequence and fiber orientation were varied parametrically. Moiré techniques were developed which allowed observation of displacements on both the wide surface and along the narrow edge of 1 in.-wide × 16-ply-thick (.085 in.-.105 in.) laminates.     

Convection heat transfer of closely-spaced spheres with surface blowing

A validated computer simulation model has been developed for the analysis of colinear spheres in a heated gas stream. Using the Galerkin finite element method, the steady-state Navier-Stokes and heat transfer equations have been solved describing laminar axisymmetric thermal flow past closely-spaced monodisperse spheres with fluid injection. Of interest are the coupled nonlinear interaction effects on the temperature fields and ultimately on the Nusselt number of each sphere for different free stream Reynolds numbers (20 ≤Re ≤ 200) and intersphere distances (1.5 ≤d _ij ≤ 6.0) in the presence of surface blowing (0 ≤v _b < 0.1). Fluid injection (i.e. blowing) and associated wake effects generate lower average heat transfer coefficients for each interacting sphere when the Reynolds number increases (Re>100). Heat transfer is also reduced at small spacings especially for the second and third sphere. A Nusselt number correlation for each interacting (porous) sphere has been developed based on computer experiments.     

The Trefftz method using fundamental solutions for biharmonic equations

In this paper, the Trefftz method of fundamental solution (FS), called the method of fundamental solution (MFS), is used for biharmonic equations. The bounds of errors are derived for the MFS with Almansi’s fundamental solutions (denoted as the MAFS) in bounded simply connected domains. The exponential and polynomial convergence rates are obtained from highly and finitely smooth solutions, respectively. The stability analysis of the MAFS is also made for circular domains. Numerical experiments are carried out for both smooth and singularity problems. The numerical results coincide with the theoretical analysis made. When the particular solutions satisfying the biharmonic equation can be found, the method of particular solutions (MPS) is always superior to the MFS and the MAFS, based on numerical examples. However, if such singular particular solutions near the singular points do not exist, the local refinement of collocation nodes and the greedy adaptive techniques can be used for seeking better source points. Based on the computed results, the MFS using the greedy adaptive techniques may provide more accurate solutions for singularity problems. Moreover, the numerical solutions by the MAFS with Almansi’s FS are slightly better in accuracy and stability than those by the traditional MFS. Hence, the MAFS with the AFS is recommended for biharmonic equations due to its simplicity.     

Self-assembly and redox modulation of the cavity size of an unusual rectangular iron thiolate aryldiisocyanide metallocyclophane

The decarbonylation reaction of ferric carbonyl dicationic [Cp(2)Fe(2)(μ-SEt)(2)(CO)(2)](BF(4))(2) [1(BF(4))(2)] carried out in refluxing acetonitrile affords a binuclear iron-sulfur core complex [Cp(2)Fe(2)(μ-SEt)(2)(CH(3)CN)(2)](BF(4))(2) [2(BF(4))(2)] containing two acetonitrile coordinated ligands. The treatment of 2(BF(4))(2) with 2 equiv of the 1,4-diisocyanobenzene (1,4-CNC(6)H(4)NC) results in the formation of the diisocyanide complex [Cp(2)Fe(2)(μ-SEt)(2)(1,4-CNC(6)H(4)NC)(2)](BF(4))(2) [3(BF(4))(2)]. The rectangular tetranuclear iron thiolate aryldiisocyanide metallocyclophane complex [Cp(4)Fe(4)(μ-SEt)(4)(μ-1,4-CNC(6)H(4)NC)(2)](BF(4))(4) [4(BF(4))(4)] has been synthesized by a self-assembly reaction between equimolar amounts of 2(BF(4))(2) and 1,4-diisocyanobenzene or by a stepwise route involving mixing of a 1:1 molar ratio of complexes 2(BF(4))(2) and 3(BF(4))(2). Chemical reduction of 4(BF(4))(4) by KC(8) was observed to produce the reduction product 4(BF(4))(2). The spectroscopic and electrochemical properties of the iron-sulfur core complexes 1(PF(6))(2), 3(BF(4))(2), 4(BF(4))(4), and 4(BF(4))(2) were determined. Finally, differences between the redox control cavities of rectangular tetranuclear iron thiolate aryldiisocyanide complexes are revealed by a comparison of the X-ray crystallographically determined structures of complexes 4(BF(4))(4) and 4(BF(4))(2).     

SnO2 nanosheets grown on graphene sheets with enhanced lithium storage properties

We demonstrate a new hydrothermal method to directly grow SnO(2) nanosheets on a graphene oxide support that is subsequently reduced to graphene. This unique SnO(2)/graphene hybrid structure exhibits enhanced lithium storage properties with high reversible capacities and good cycling performance.     

Instantaneous room-temperature and highly enantioselective ArTi(O-i-Pr)3 additions to aldehydes

Direct asymmetric additions of ArTi(O-i-Pr)(3) to aldehydes catalyzed by a titanium catalyst of (R)-H(8)-BINOL are reported. The reactions proceed instantaneously at room temperature, affording alcohols in ≥90% ee. Importantly, the ArTi(O-i-Pr)(3) reagent differentiates the ligand effectiveness in an order of H(8)-BINOL > BINOL > TADDOL > diol 3 > disulfonamide 2.     

Large Femtosecond Two-Photon Absorption Cross-Sections of Fullerosome Vesicle Nanostructures Derived from Highly Photoresponsive Amphiphilic C(60)-Light-Harvesting Fluorene Dyad

We demonstrated ultrafast femtosecond nonlinear optical (NLO) absorption characteristics of bilayered fullerosome vesicle nanostructures derived from molecular self-assembly of amphiphilic oligo(ethylene glycolated) C(60)-(light-harvesting diphenylaminofluorene antenna). Fullerene conjugates were designed to enhance photoresponse in a femtosecond time scale by applying an isomerizable periconjugation linker between the C(60) cage and diphenylaminofluorene antenna subunit in an intramolecular contact distance of only < 3.0 ?. Morphology of C(60)(>DPAF-EG(12)C(1))-based fullerosome nanovesicles in H(2)O was characterized to consist of a bilayered shell with a sphere diameter of 20-70 nm and a chromophore shell-width of 9.0-10 nm, fitting well with a head-to-head packing configuration of the molecular length. At the estimated effective nanovesicle concentration as low as 5.5 × 10(-8) MV (molecular molar concentration of 5.0 × 10(-4) M) in H(2)O, two-photon absorption (2PA) phenomena were found to be the dominating photophysical events showing a large molar concentration-insensitive 2PA cross-section value equivalent to 8500 GM in a form of nanovesicles, on average. The observed NLO characteristics led to a sharp trend of efficient light-transmittance intensity reduction at the input laser intensity above 100 GW/cm(2).     

Isolation and identification of beta-hydroxyethylaprophen: a urinary metabolite of aprophen in rats

The metabolism of the anticholinergic drug aprophen was studied in rats after oral administration via stomach intubation. beta-Hydroxyethylaprophen, a major urinary metabolite of aprophen, was isolated and identified by normal-phase high-performance liquid chromatography and electron ionization mass spectrometry. More than 22% of the parent drug was recovered and quantified over a 72-h collection period. Results show that 2,2-diphenylpropionic acid, another major metabolite of aprophen which lacks anticholinergic properties, was also isolated and identified in this study. Experiments are currently underway to synthesize and test the anticholinergic properties of beta-hydroxyethylaprophen in mammals.