半导体激光器的超高频调制

本文从理论上分析了半导体激光器的超高频调制特性和脉动电流引起的张弛振荡现象。分析了国产DHGaAlAs半导体激光器调制过程中出现的一些问题。实验证明,采用微带匹配技术,可使这类激光器的调制频率达1.3GHz。     

WEAK CONVERGENCE OF SOME DIRICHLET SERIES

1 Besicovitch Inner ProductIll this paper, we consider Dirichlet serie8where an, tL = 1, 2,' ', are complex nunlbers. They are Besicovitch almost periodic functionsWe see the 8ystenl {e.(t); e.(t) = e--it Iog 1l, 71 = l, 2,' .} fOrnis a1l orthollor11la1 systelll witl1respect to tI1e BesicovitcI1 iIl1ler productThell we call fOrm the gelleralized trigouolnetrical polynolIlialsAccording to tl1e idea developed il1 [l],[2], auy Dirichlet seriesis weakly convergent over K witll respect to …     

Synthesis and Characterization of A Novel Cholesteric Liquid Crystalline Containing Carboxyl Group

A novel liquid crystal compound with a carboxyl group at one end, cholest-5-en-3-ol-(3β) hydrogen decanedioate (1) was successfuly prepared by the reaction of cholesterol with sebacoxl chloride. Its chemical structure and liquid crystalline properties were characterized by FTIR.CNMR,HNMR,POM and DSC. The compound with an active carboxyl group shows themortropic liquid crystalline behaviour.     

氟代糖的合成

本文综述了氟代糖合成的新进展及利用选择性氟化合成具有生物活性的物质。     

FeCl_3·6H_2O Catalyzed Reaction of Aromatic Aldehydes with 5, 5-Dimethyl-1, 3-cyclohexandione in Ionic Liquids

Room temperature ionic liquids with low melting point (<100℃) salts represent a new class of non-molecular, ionic solvents. Especially those based on the 1-N-alkyl-3- methylimidazolium cations, have shown great promise as an attractive alternative to conventional solvents for catalytic reactions1. On the other hand, FeCl3·6H2O was considered to be an environmentally benign Lewis acid and has been used successfully in several kinds of organic reactions2. Recently we have focused our interes…     

Synthesis of polyethylene‐octene elastomer/SiO2‐TiO2 nanocomposites via in situ polymerization: Properties and characterization of the hybrid

In this study, a silicic acid and tetra isopropyl ortho titanate ceramic precursor and a metallocene polyethylene‐octene elastomer (POE) or acrylic acid grafted metallocene polyethylene‐octene elastomer (POE‐g‐AA) were used in the preparation of hybrids (POE/SiO₂? TiO₂ and POE‐g‐AA/SiO₂? TiO₂) using an in situ sol‐gel process, with a view to identifying a hybrid with improved thermal and mechanical properties. Hybrids were characterized using Fourier transform infrared spectroscopy, ²⁹Si solid‐state nuclear magnetic resonance (NMR), X‐ray diffraction, differential scanning calorimetry, thermogravimetry analysis, dynamic mechanical thermal analysis, and Instron mechanical testing. Properties of the POE‐g‐AA/SiO₂? TiO₂ hybrid were superior to those of the POE/SiO₂? TiO₂ hybrid. This was because the carboxylic acid groups of acrylic acid acted as coordination sites for the silica‐titania phase to allow the formation of stronger chemical bonds. ²⁹Si solid‐state NMR showed that Si atoms coordinated around SiO₄ units were predominantly Q₃ and Q₄. The 10 wt % SiO₂? TiO₂ hybrids gave the maximum values of tensile strength and glass transition temperature in both POE/SiO₂? TiO₂ and POE‐g‐AA/SiO₂? TiO₂. It is proposed that above this wt %, excess SiO₂? TiO₂ particles caused separation between the organic and inorganic phases. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1690–1701, 2005     

The effects of melt annealing and counterpart's molecular weight on the thermal properties and phase morphology of poly(L‐lactide)‐based blends

The thermal properties and phase morphology of poly(L ‐lactide) (PLLA)‐based blends have been studied. Two poly(ethylene glycol)s (PEGs) with molecular weight (MW) of about 1,500 (1.5k) g/mol and 2,000,000 (2M) g/mol, respectively, were used as counterparts. The blends were annealed at a preselected temperature of 200 °C for either 2 min or 30 min before the characterizations. Both PEGs were determined to enhance the crystallizability of PLLA. After a 2‐min process of annealing, the PEG(1.5k)'s crystallization efficiency on PLLA has been noted to increase with the increase of its content. Conversely, PEG(2M)'s crystallization efficiency declined with the increase of its content. Extending the annealing time has evidently changed the PEGs' crystallization effect on PLLA. Moreover, the PEG(1.5k) has, to a greater extent, brought about the depression of PLLA's melting temperature by increasing its content, and this depression increased with the annealing time. The blends exhibited lower thermal stability than those of the parent components, particularly for the PEG(1.5k)‐included system with a higher PEG content. Regardless of the annealing time, the PEG(1.5k)‐included blends have shown homogeneous melt morphology under light microscope, whereas the PEG(2M)‐included blends have displayed phase‐separated melt morphology. In addition to the composition, PEG's MW and annealing time influence the crystalline morphology of the blends. The ringed PLLA spherulites have appeared mostly in the 2‐min annealed PEG(1.5k)‐included blends. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 1497–1510, 2009     

Facile method to prepare monodispersed Ag/polystyrene composite microspheres and their properties

This article presents a facile method to prepare silver/polystyrene composite microspheres. In this approach, monodispersed polystyrene (PS) particles were synthesized with carboxyl acid groups on the surfaces of the PS particles via dispersion polymerization at first. With the addition of [Ag(NH₃)₂]⁺ to the PS dispersion, [Ag(NH₃)₂]⁺ was absorbed to the surfaces of the PS particles, and then by heating the system, [Ag(NH₃)₂]⁺ complex ions were reduced to silver to form the Ag/PS composite microspheres. In the synthesis of PS dispersion, PVP was used as dispersant to stabilize the PS particles, it also acted as reducing agent in the reduction of [Ag(NH₃)₂]⁺ complex ions to silver, so no additional reducing agent was needed. The resulting composite microspheres were characterized by TEM, SEM, XPS, and XRD. The catalytic properties and surface‐enhance Raman scattering (SERS) was studied as well. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 4547–4554, 2009