A new design of nanocrystalline silicon optical devices based on 3-dimensional photonic crystal structures

We propose a new design of nanocrystalline silicon optical devices which are based on control of electromagnetic fields, electronic states, as well as the phonon dispersion of size-controlled silicon quantum dots

Solution and gelling properties of gellan benzyl esters

Gellan benzyl esters of different degrees of esterification were prepared, and their gelation behavior was examined. Native gellan and gellan benzyl ester aqueous solutions and the ensuing aqueous gels obtained by cooling their solutions with added salt were studied by means of rheological and small-angle X-ray scattering experiments. Although esterification causes no fundamental changes in the gellan ordered structure, the introduction of bulky benzyl ester groups reduces the backbone propensity of double-helix formation and subsequent helix-helix association (gelation). In consequence, gellan-based gels become less stable both mechanically and thermally with esterification

Mesophase structure discovered through in-situ X-ray measurement in drawing process of poly(ethylene 2,6-naphthalene dicarboxylate) fiber

The structure development in the continuous laser-heated drawing process of poly(ethylene 2,6-naphthalene dicarboxylate) (PEN) fiber was analyzed by in-situ X-ray diffraction measurement. Because of the rapid and uniform laser heating, and the resultant steady-state nature of the necking-drawing, the structure development after the on-set of necking could be measured in the time resolution of several hundred microseconds. We found for the first time the temporal appearance of meridional (001') diffraction at several milliseconds after the on-set of necking indicating that the mesophase structure similar to the one reported for poly(ethylene terephthalate) was also formed in the initial stage of fiber structure development of PEN. The d-spacing of the (001') diffraction 1.230 +/- 0.003 nm was shorter than the c-axis lengths of both alpha and beta crystals.ArticlePOLYMER. 50(19):4429-4431 (2009)journal articl

In-situ analysis of fiber structure development for isotactic polypropylene

Structural development of isotactic polypropylene (iPP) fibers was analyzed in real time through in-situ WAXD/SAXS and fiber temperature measurements during CO(2) laser-heated drawing because the CO(2) laser irradiation can nearly fix the necking position on the running fiber. The in-situ WAXD/SAXS measurements were carried out with a high time-resolution of 0.4 ms. The as-spun iPP fibers of two different initial structures were laser-heat-drawn to a draw ratio of 6.5. For the drawing of PP fiber containing mesophase structure, diffraction from the oriented mesophase remained until an elapsed time of 1.0 ms, when oriented alpha-phase crystal started to form. Meanwhile, for the drawing of PP fiber containing both an alpha-phase and a mesophase structure, fragmented microcrystals were reorganized by orientation-induced crystallization before an elapsed time of 1.0 ms. The long period increased drastically with fragmentation, and decreased with reorganization. The long period was about 16 nm for both drawn fibers.ArticlePOLYMER. 52(9):2044-2050 (2011)journal articl

Effect of drawing stress on mesophase structure formation of poly(ethylene 2,6-naphthalene dicarboxylate) fiber just after the neck-drawing point

The structural development of poly(ethylene 2,6-naphthalene dicarboxylate) (PEN) fibers was analyzed by in situ X-ray diffraction and fiber temperature measurements. The PEN fiber was drawn continuously under three drawing stresses, where the neck-drawing point was fixed accurately by CO2 laser irradiation heating. The developed crystal structures of the drawn fibers depended on the drawing stresses, that is, only the alpha-crystal was obtained under a drawing stress of 148 MPa, an alpha-rich mixed crystal was obtained for 54 MPa, and a beta-rich mixed crystal was obtained under 23 MPa stress. Fiber containing over 70% beta-crystal was obtained in the third case. Orientation-induced crystallization rates (K) and crystallization induction times (t(0)) were estimated for the three drawing stresses: K = 2210 s(-1) and t(0) = 0.5 ms for 148 MPa, K = 940 s(-1) and t(0) = 1.0 ms for 54 MPa, and K= 655 s(-1) and t(0) = 4.0 ms for 23 MPa. In addition, the drawing stress acted as a definitive influence not only on the resulting crystal form but also on the chain conformation of the mesophase structure. The d-spacing of the (001') diffraction increased with drawing stress, and the longer (001') spacing generated the alpha-crystal while the comparatively shorter (001') spacing yielded the beta-crystal. The d-spacings of 1.27 and 1.23 nm for the drawing stresses of 148 and 23 MPa, respectively, were somewhat shorter than the c-axis lengths of the alpha- and beta-crystals of 1.32 and 1.27 nm, respectively.ArticlePOLYMER. 53(19):4272-4279 (2012)journal articl

Development of a fiber structure in poly(vinylidene fluoride) by a CO(2) laser-heated drawing process

Rapid and uniform heating by CO(2) laser radiation can fix the position where necking occurs. Therefore, this study investigated the development of a fiber structure in poly(vinylidene fluoride) in continuous drawing by in situ measurement using synchrotron X-ray radiation with a time resolution of several hundred microseconds. Two neck-deformation behaviors were observed in the laser drawing: a moderate neck deformation under low drawing stress and a steep neck deformation under high drawing stress. The low drawing stress resulted in a mixture of alpha- and beta-crystals in which the beta-crystal was formed within 1ms after the necking, earlier than the alpha-crystal. The development of the fiber structure under high drawing stress was almost complete in less than 1 ms, and the developed structure contained only beta-crystals. Small-angle X-ray scattering images showed meridional streaks at low drawing stress, whereas a four-pointed pattern occurred under high drawing stress. Low drawing stress generated a long periodic structure that was defective in the periodic regularity of crystalline and amorphous regions, although the molecular chains were nearly oriented along the fiber axis. The high drawing stress resulted in a well-packed structure of adjacent fibrils with alternating amorphous and crystalline regions. Polymer Journal (2010) 42, 657-662; doi: 10.1038/pj.2010.53; published online 23 June 2010ArticlePOLYMER JOURNAL. 42(8):657-662 (2010)journal articl

Direct interaction of insulin-like growth factor-1 receptor with leukemia-associated RhoGEF

Insulin-like growth factor (IGF)-1 plays crucial roles in growth control and rearrangements of the cytoskeleton. IGF-1 binds to the IGF-1 receptor and thereby induces the autophosphorylation of this receptor at its tyrosine residues. The phosphorylation of the IGF-1 receptor is thought to initiate a cascade of events. Although various signaling molecules have been identified, they appear to interact with the tyrosine-phosphorylated IGF-1 receptor. Here, we identified leukemia-associated Rho guanine nucleotide exchange factor (GEF) (LARG), which contains the PSD-95/Dlg/ZO-1 (PDZ), regulator of G protein signaling (RGS), Dbl homology, and pleckstrin homology domains, as a nonphosphorylated IGF-1 receptor-interacting molecule. LARG formed a complex with the IGF-1 receptor in vivo, and the PDZ domain of LARG interacted directly with the COOH-terminal domain of IGF-1 receptor in vitro. LARG had an exchange activity for Rho in vitro and induced the formation of stress fibers in NIH 3T3 fibroblasts. When MDCKII epithelial cells were treated with IGF-1, Rho and its effector Rho-associated kinase (Rho-kinase) were activated and actin stress fibers were enhanced. Furthermore, the IGF-1–induced Rho-kinase activation and the enhancement of stress fibers were inhibited by ectopic expression of the PDZ and RGS domains of LARG. Taken together, these results indicate that IGF-1 activates the Rho/Rho-kinase pathway via a LARG/IGF-1 receptor complex and thereby regulates cytoskeletal rearrangements