Synthesis and characterization of monodisperse magnetic composite particles for magnetorheological fluid materials

Monodisperse magnetic composite particles (MCP) were prepared and characterized for a study of magnetic field-responsive fluids. Magnetic composite particles used are iron oxide-coated polymer composite particles, which were synthesized through in situ coating of iron oxide onto pre-existing polymer particles by the reduction of ferrous fluids. For a uniform and bulk coating of iron oxide, the porous structure was introduced into the substrate polymer particles through a two-step seeded polymerization method. Moreover, surface cyano-functionality was born from acrylonitrile unit of substrate polymer and it played an important role in obtaining successful uniform coating. The structure of the composite particle was analyzed by using a thermo gravimetric analysis (TGA) and a X-ray diffraction (XRD) analysis. The magnetization property of the particle was also observed. Then, the rheological properties of monodisperse magnetorheological (MR) suspensions of magnetic composite particles were examined under a magnetic field using a parallel-plate type commercial rheometer. From the rheological measurements, it was found that MR properties of the magnetic composite suspensions are dependent on the iron oxide content and the fluid composition.     

Mechanical properties of amphiphilic urethane acrylate ionomer hydrogels having heterophasic gel structure

Amphiphilic urethane acryale hydrogels containing ionic groups (dimethylolpropionic acid) were prepared by varying the molecular weight of the soft segment (polyether type) and the type of diisocyanate, and their mechanical properties were examined. They showed heterophasic gel structure composed of ionic hard domains induced by aggregation of the ionic groups and polyether soft domains comprising the urethane acrylate network. This heterophasic structure could be confirmed by dynamic mechanical analysis (DMA) and by wide-angle X-ray scattering analysis (WAXS); the crystallinity detected by WAXS and the transition peak of the ionic hard domains detected by DMA strongly suggested that there were ionic aggregates. These ionic aggregates acted as reinforcing fillers in the network, which eventually enhanced the tensile strength of the hydrogels. Above all, the tensile properties of the hydrogels were of interest in that the trends of the stress-strain curves were consistent with the rubbery ones. It is believed that the higher purity of the polyether soft domains resulted from the heterophasic gel structure imparting further elastomeric properties on the network. Received: 31 July 1998 Accepted in revised form: 15 October 1998     

Synthesis of novel conjugated polymer based on cyclopenta[def]phenanthrene and vinylene with strong interchain interaction

In this study, a novel conjugated polymer, poly(4,4‐bis(2‐ethylhexyl)‐4H‐cyclopenta[def]phenanthrene‐2,6‐vinylene) (PCPPV) has been synthesized and characterized. For the polymerization, Gilch's reaction was applied for the first time with the cyclopenta[def]phenanthrene system. The absorption and emission spectra of PCPPV are red‐shifted about 40–50 nm due to the vinylene units when compared with those of poly(2,6‐(4,4‐bis(2‐ethylhex‐yl)‐4H‐cyclopenta[def]phenanthrene)) (PCPP). The solid‐state fluorescence is significantly broadened, possibly due to π–π interactions introduced by the phenanthrene and vinylene moieties. In solution, as the concentration of polar solvent increased, the photoluminescence (PL) intensity decreased due to quenching and aggregation by the interchain interactions between the conjugated backbones. After annealing the film at 80 °C, the PL and electroluminescence (EL) emission spectra exhibited also the quenching and aggregation effects indicating the interchain interactions of PCPPV. The large number of aromatic rings in a unit and the increased planarity achieved through introduction of vinylene units are able to give interchain interactions stronger than fluorene or phenylene units. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 5068–5077, 2009     

Error analysis of the L2 least‐squares finite element method for incompressible inviscid rotational flows

In this article we analyze the L² least‐squares finite element approximations to the incompressible inviscid rotational flow problem, which is recast into the velocity‐vorticity‐pressure formulation. The least‐squares functional is defined in terms of the sum of the squared L² norms of the residual equations over a suitable product function space. We first derive a coercivity type a priori estimate for the first‐order system problem that will play the crucial role in the error analysis. We then show that the method exhibits an optimal rate of convergence in the H¹ norm for velocity and pressure and a suboptimal rate of convergence in the L² norm for vorticity. A numerical example in two dimensions is presented, which confirms the theoretical error estimates. © 2004 Wiley Periodicals, Inc. Numer Methods Partial Differential Eq, 2004     

Mechanics of rubber shear springs

FEA calculations have been carried out for a model rubber shear spring, consisting of a block of a highly elastic material, bonded between two rigid parallel plates and sheared by displacing one of the plates parallel to the other in its own plane. The block was prevented from deforming in the perpendicular direction, and thus was deformed in plane strain. Stress distributions along the bond-line and the center-line are reported and compared with those expected from the theory of large elastic deformations. Unexpected tensile stresses were found to develop in the interior of the sheared block. They are attributed to the absence on the end surfaces of the stresses needed to maintain a simple shear, causing a pronounced change in the reference pressure—a consequence that is usually overlooked. Because the internal stresses are governed by the boundary conditions, they were strongly affected by the shape of the end surfaces. In addition, they were reduced markedly by assigning values to Poisson's ratio slightly lower than 0.5, thus allowing some volume expansion of the rubber. Strain energy release rates were also evaluated for growth of a crack along the bond-line, starting at the edges, and compared with those reported previously by Lindley and Teo [Energy for crack growth at the bonds of rubber springs, Plast. Rubber Mat. Appl. 4 (1979) 29-37], Muhr et al. [A fracture mechanics study of natural rubber-to-metal bond failure, J. Adhes. Sci. Technol. 10 (1996) 593-616], Gregory and Muhr [Stiffness and fracture analysis of bonded rubber blocks in simple shear, in: D. Boast, V.A. Coveny (Eds.), Finite Element Analysis of Elastomers, Professional Engineering Publications, Bury St. Edmunds, UK, 1999, pp. 265-274] and Gough and Muhr [Initiation of failure of rubber close to bondlines, in: Proceedings of the International Rubber Conference, Maastricht, Netherlands, June 2005, IOM Communications Ltd., London, 2005, pp. 165-174]. They confirm that a long crack at the compression edge will grow faster than one at the tension edge, but the results for short cracks were inconclusive.     

Three New Lignan Derivatives from Lindera glauca (Siebold et Zucc.) Blume

Two new aryl‐tetralin lignan glycosides, linderanosides A and B ( 1 and 2 , resp.), and a new dihydrobenzofuran neolignan glycoside, linderanoside C ( 3 ), together with five known lignan derivatives ( 4 – 8 ) were isolated from the trunk of Lindera glauca. The structures of these new compounds were determined through spectroscopic analyses, including extensive 2D‐NMR data and acid hydrolysis. The absolute configurations of the compounds were clarified by circular dichroism (CD) spectroscopic studies. Compounds 1 – 8 were evaluated for their cytotoxicity against A549 (non‐small cell lung adenocarcinoma), SK‐OV‐3 (ovarian cancer cells), A498 (human kidney epithelial cells), and HCT‐15 (colon cancer cells) human tumor cell lines using sulforhodamine B assays in vitro.     

Helical silica nanotubes: Nanofabrication architecture,transfer of helix and chirality to silica nanotubes

A series of neutral gelators and cationic amphiphiles derived from 1,2 diphenylethylenediamine (I) and 1,2-cyclohexanediamine (II) was synthesised. Helical silica nanotubes were prepared utilising these organic gelators through sol-gel polycondensation of tetraethoxy silane, (TEOS-silica source). Right- and left-handed helical nanotubes respectively were obtained from a 1: 1 mass mixture of optically active, (1S,2S)-III-(1S,2S)-V neutral gelator and (1S,2S)-IV-(1S,2S)-VI cationic amphiphile and a 1: 1 mass mixture of optically active, (1R,2R)-III-(1R,2R)-V neutral gelator and (1R,2R)-IV-(1R,2R)-VI cationic amphiphile, indicating that the handedness of the helical nanotubes varied with the change in the neutral gelator precursors used. The nanotubes were characterised by SEM images.     

Multiscale fabrication of multiple proteins and topographical structures by combining capillary force lithography and microscope projection photolithography

We present new methods that enable the fabrication of multiscale, multicomponent protein-patterned surfaces and multiscale topologically structured surfaces by exploiting the merits of two well-established techniques: capillary force lithography (CFL) and microscope projection photolithography (MPP) based on a protein-friendly photoresist. We further demonstrate that, when hierarchically organized micro- and nanostructures were used as a cell culture platform, human colon cancer cells (cell line SW480) preferentially adhere and migrate onto the area with nanoscale topography over the one with microscale topography. These methods will provide many exciting opportunities for the study of cellular responses to multiscale physicochemical cues.