Directional coupling of optical signals by odd dark beams with mixed phase dislocations

Numerical simulations on the evolution of step-screw and edge-screw optical phase dislocations in bulk saturable self-defocusing nonlinear media are presented, with emphasis on their ability to induce steering waveguides for signal beams (pulses). Two schemes for directional coupling of such signals, both ensuring a reasonable coupling-to-cross-talk efficiency ratio, are investigated. The parameters useful for performance optimization of the couplers are discussed. Received: 19 July 2000 / Revised version: 5 February 2001 / Published online: 27 April 2001     

Systematics of related high-spin isomers in 144Sm and other N = 82 nuclei

An in-beam experiment with the reaction ¹²²Sn(²⁷Al,4np) at 127 MeV was performed at the Nordball multi-detector array in Roskilde. It provided evidence for a new high-spin isomer in ¹⁴⁴Sm. This isomer with T _1/2= (2.6 ± 0.5) ns at an excitation energy E _x= 9232 keV seems to belong to a family of isomers of similar configuration in neighbouring N= 82 nuclei. Received: 16 November 1997     

Alpha-decay half-life of <Superscript>221</Superscript>Fr in different environments

A possible dependence of the alpha decay process on the solid-state environment of the decaying nucleus has been investigated by measuring the alpha-decay half-life of ²²¹Fr at room temperature in different materials ( Au, W, Si and polyethylene). The change in half-life between the insulator Si and the metals Au/ W is found to be 0.30(17)% / 0.42(21)%, respectivly. Furthermore an improved value of 4.79(2)min was found for the absolute half-life of ²²¹Fr.     

Shape coexistence near the double-midshell nucleus 111Rh

The decay of ¹¹¹Ru obtained from fast on-line chemical and mass separation has been investigated by β-γ-t and γ-γ coincidence techniques. Earlier spin and parity assignments of ¹¹¹Rh levels based on extrapolations of level systematics are confirmed. In particular, the K=1/2 intruder band is supported by the hindrance of E2 transitions between deformed and spherical states and enhancement of intraband E2 transitions. The excitation energies of intruder band members in Rh isotopes show a minimum at ¹⁰⁹Rh₆₄, with two neutrons less than ¹¹¹Rh at the N=66 midshell. This trend, which differs from the one in the higher-Z neighbouring elements Ag and Cd with minima at N=66, follows the evolution of deformation observed in the lower-Z elements Ru and Mo. Received: 25 June 1997 / Revised version: 10 September 1997     

PEEK碳纤维增强复合材料的动态力学行为

ＰＥＥＫ碳纤维增强复合材料的动态力学行为李健（中国科学院固体物理研究所合肥２３００３１）章明秋，徐建军（中山大学材料科学研究所广州）（青岛化工学院青岛）关键词ＰＥＥＫ，碳纤维复合材料，内耗，Ｔｇ热塑性、耐高温的工程塑料聚醚醚酮（ＰＥＥＫ）是一种半晶聚...     

Shape changes at high spin in 78Kr

High-spin states in ⁷⁸Kr have been studied via the ⁶³Cu (¹⁹F, 2p2n)⁷⁸Kr reaction at a beam energy of 60 MeV using the Indian National Gamma Array (INGA). In this nucleus, lifetimes have been measured upto the I^π=22⁺ level in the yrast positive-parity band and upto the I^π=15^- level in the negative-parity band using the Doppler Shift Attenuation Method (DSAM). The deduced transition quadrupole moments Q_t's are found to decrease with rotational frequency for both the bands.     

Benzylated pulps from sugar cane bagasse

An optimized ethanol/water process has been employed for the pulping of fibres from sugar cane bagasse. After pretreatment with aqueous NaOH, unbleached pulps were subjected to benzylation at 110 °C for different periods of time. The resulting purified products were characterized by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), gel permeation chromatography (GPC) and infrared spectroscopy (IR). The results showed that benzylation proceeded to various extents depending on the reaction time, as assessed by weight gain. During the first 3 h, a loss of mass was observed due to the occurrence of benzylation of low molecular weight polyoses, which were eliminated in the purification step. After that period of time a drastic weight increase was observed probably because crystalline regions had developed. The samples with low degrees of benzylation were insoluble, whereas the more benzylated counterparts showed limited solubility in THF. Partially soluble samples and a completely soluble one showed very different GPC elution profiles. This may be attributed to the efficiency of the pre treatment which, in the latter case, employed more concentrated alkali. Thermogravimetric analyses showed that all samples were degraded above 310 °C. Glass transition temperatures ranged between 42 °C and 65 °C, increasing as the extent of benzylation increased This revised version was published online in August 2006 with corrections to the Cover Date.     

环氧交联网T_g转变的tanδ-T曲线解析

本文系统地研完了预聚物分子量、固化剂配比和固化条件对环氧交联网T_g松弛内耗峰松弛时间分布的影响。本实验和理论研究结果首次证明了环氧交联网T_g松弛过程具有单一松弛时间描述的线性标准固体的特征,与预聚体分子量、固化剂配比和固化条件无关。此结果可用环氧交联网的两相结构特征加以解释。     

Property modification of poly(methyl methacrylate) through copolymerization with fluorinated aryl methacrylate monomers

Copolymers of methyl methacrylate (MMA) with 2,3,5,6‐tetrafluorophenyl methacrylate (TFPMA), pentafluorophenyl methacrylate (PFPMA), and 4‐trifluoromethyl‐2,3,5,6‐tetrafluorophenyl methacrylate (TFMPMA) were investigated. All the three systems showed a random copolymerization character. The composition, glass transition temperature (T_g), and refractive index of the copolymers obtained were studied. T_gs of TFPMA/MMA and PFPMA/MMA copolymers were found to deviate positively from the Gordon–Taylor equation. However, T_gs of TFMPMA/MMA copolymers were well fit with the Gordon–Taylor equation. These results indicated the existence of interaction between MMA and either TFPMA or PFPMA units in copolymers. This interaction resulted in the enhancement of the T_g of MMA polymers through the copolymerization with TFPMA and PFPMA. The refractive index and the light transmittance of copolymers were close to those of PMMA. Copyright © 2007 John Wiley & Sons, Ltd.     

Covalent fixed multicyclic polystyrene conformers

Covalent fixed multicyclic polystyrene conformers were synthesized from inconvertible polystyrene conformers based on p‐tert‐butylthiacalix[4]arene by azidation and subsequent click coupling. Selective 1D NOESY analyses confirmed that the spatial structures of star polystyrene precursors and multicyclic polystyrenes were preserved during the azidation and click coupling processes. The conformation of star polymers affected degree of decrease in the hydrodynamic volume after cyclization but had little effect on glass transition behavior. The rigid core of star polymer increased the T_g but in the case of multicyclic polymer, this influence of core structure was reduced. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 4020–4026