Microstructure effect in the coupling reactions of polymeric organolithium compounds using chlorosilanes

The most important variable affecting the yield in the coupling reactions of polymeric organolithium compounds with chlorosilane compounds has been investigated through size-exclusion chromatographic (SEC) analysis. The coupling reaction of poly(styryl)lithium with dichlorodimethylsilane as a silane-coupling agent provided 44 wt % of the coupling yield. The coupling yield, depending on the chain end reactivity of active polymers, was not greatly affected. The addition of a Lewis base such as N,N,N′,N′-tetramethylethylenediamine (TMEDA) even after complete polymerization of the dienes in hydrocarbon seems to affect the coupling reaction, resulting in decreasing the yield. The 1,2- or 3,4-enchain contents in the polydiene backbones affected the reduction of the linking efficiency in the coupling of the poly(dienyl)lithiums with chlorosilanes as the linking agent. The linking yields of the active polymers including over 75 mol % of 1,2- or 3,4-enchainment on the polydiene segment were below 20 wt %. The linking yields exhibited a dependence not only on the steric requirement of the chain end, but also the microstructure of the polydiene segment. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1743–1753, 1998     

Details of surface features in aromatic polyamide reverse osmosis membranes characterized by scanning electron and atomic force microscopy

In the present article, some new events on the surface morphology of the aromatic polyamide thin‐film‐composite (TFC) membranes were demonstrated in conjunction with their inherent chemical nature. In addition, the detailed, quantitative understanding of the microscopic surface features was shown to be essential in controlling the water permeability and eventually developing the high performance membranes. The surface roughness and the surface area were mainly affected by the existence or nonexistence of the crosslinking and/or the free amide groups not pertinent to the formation of the hydrogen bonding, which in turn contributed to the water permeability. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 1429–1440, 1999     

Simulation of three-point bending at large deflections by an elastoplastic contact analysis

Three-point bending is simulated by an elaborate numerical procedure based on an elastoplastic, large deflection, contact analysis. A minimization formulation is used, which is equivalent to the incremental form posed as partial differential equations with inequalities. A sequential quadratic programming approach based on the finite-element technique is adopted as a method of solution. To examine the validity of the simulation method, experiments are carried out for specimens that have various widths.Paper was presented at the 1988 SEM Spring Conference on Experimental Mechanics held in Portland, OR on June 5–10.     

s‐Regular cubic graphs as coverings of the complete bipartite graph K3,3

A graph is s‐regular if its automorphism group acts freely and transitively on the set of s‐arcs. An infinite family of cubic 1‐regular graphs was constructed in [10], as cyclic coverings of the three‐dimensional Hypercube. In this paper, we classify the s‐regular cyclic coverings of the complete bipartite graph K_3,3 for each ≥ 1 whose fibre‐preserving automorphism subgroups act arc‐transitively. As a result, a new infinite family of cubic 1‐regular graphs is constructed. © 2003 Wiley Periodicals, Inc. J Graph Theory 45: 101–112, 2004     

Classifying cubic symmetric graphs of order 10p or 10p2

A graph is called s-regular if its automorphism group acts regularly on the set of its s-arcs. In this paper, the s-regular cyclic or elementary abelian coverings of the Petersen graph for each s ⩾ 1 are classified when the fibre-preserving automorphism groups act arc-transitively. As an application of these results, all s-regular cubic graphs of order 10p or 10p ² are also classified for each s ⩾ 1 and each prime p, of which the proof depends on the classification of finite simple groups.     

Shape sensitivity analysis of thin-shell structures

This paper presents explicit formulas for shape sensitivity analysis of thin shell structures. The curvature distribution is the design to be determined. The thin-shell theory employed is the general Koiter model in the Cartesian coordinates. For the shape sensitivity formulation, both the direct differentiation method and the material derivative concept have been used. The two formulations are shown to be equivalent. A computer program based on these formulations has been developed and applied to examples. The shape sensitivity results obtained have been compared to those obtained by finite differencing.     

Synthesis and properties of blue light‐emitting,silicon‐containing,regio‐ and stereoregular conjugated polymers

This article concerns the hydrosilylation polyaddition of 1,4‐bis(dimethylsilyl)benzene ( 1 ) with 4,4′‐diethynylbiphenyl, 2,7‐diethynylfluorene ( 2b ), and 2,6‐diethynylnaphthalene with RhI(PPh₃)₃ catalyst. Trans‐rich polymers with weight‐average molecular weights (M_w's) ranging from 19,000 to 25,000 were obtained by polyaddition in o‐Cl₂C₆H₄ at 150–180 °C, whereas cis‐rich polymers with M_w's from 4300 to 34,000 were obtained in toluene at 0 °C–r.t. These polymers emitted blue light in 4–81% quantum yields. The cis polymers isomerized into trans polymers upon UV irradiation, whereas the trans polymers did not. The device having a layer of polymer trans‐ 3b obtained from 1 and 2b demonstrated electroluminescence without any dopant. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2774–2783, 2004