伽利略的自由落体定律研究——"最美丽"的十大物理实验之一

在伽利略的运动学研究中,自由落体运动是一个重要课题.他敏锐地认识到,通过打开自由落体运动这个缺口,会导致一门新科学的诞生.他在《两门新科学》(即《关于两门新科学的数学证明的对话》)一书中写道:"我的目的,是要阐述一门崭新的科学,它研究的却是非常古老的课题.也许,在自然界中最古老的课题莫过于运动了.     

Studies of some new bioactive acrylic esters

Four typical bioactive esters of acrylic monomers, N-p-acryloxybenzoyloxysuccinimides, 3-ac-ryloxy-4-oxo-3,4-dihydro-1,2,3-benzotriazines, N-acryloxy-5-norbornene-2,3-dicarboximides, and I-p-acryloxybenzoyloxybenzotriazoles, were Synthesized and polymerized as reactive polymers. Twelve new monomers were prepared by coupling acrylic acid, methacrylic acid, p-acryloxybenzoic acid, or p-methacryloxybenzoic acid with four N-hydroxy compounds such as N-hydroxysuccinimide (HOSu), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HOObt), N-hydroxy-5-norbornene-2,3-dicarboximide (HONB), and I -hydroxybenzotriazole (HOBT) in the presence of dicyclohexylcarbodimide. All monomers polymerized readily in solution with azobisisobutyronitrile (AIBN) as free radical initiator. The resulting reactive polymers with reactive ? OSu, ? OObt, ? ONB, or ? OBT group on the side chain are equally reactive toward n-butylamine at room temperature in the formation of corresponding polyacrylamides. Reactive polymers were used to immobilizetrypsin. It has been found that poly(N-p-methacryloxybenzoyloxy-5-norbornene-2,3-dicarboximide)-trypsin matrix had high activity around three times that of the poly(N-methacryloxy-5-norbornene-dicarboximide)-trypsin matrix. It is proposed that this activity may be due to the presence of a long spacer arm with a hydrophobic and rigid benzene ring between the ligand and matrix. The reactive poly(N-p-methacryloxybenzoyloxysuccinimide-p-methacryloxybenzoic acid) copolymer was used to immobilize the serum protein. This immobilized protein was a hopeful bioactive solid immunoadsorbent.     

A Study of the Dynamics of Formation of Plasmoids in the Gatchina Discharge

Technical Physics - The results of studies of the Gatchina discharge conducted at the Harbin University of Technology (China) have been presented. The Gatchina discharge is mainly used to create an...     

Lagrangian approach for dark soliton in nonlocal nonlinear media

We theoretically investigate the dynamics of dark solitons as well as their interaction in nonlocal media. Approximate equations describing the evolution of the beams are obtained via suitable trial functions of amplitude u and refractive index n in an averaged Lagrangian. Our results reveal that out-of-phase dark solitons can evolve into stable bound states in nonlocal materials. Moreover, it is found that the separations in the bound state monotonically increase with the degree of nonlocality in nonlocal limit. These results are in excellent agreement with the numerical simulations.     

自适应桁架形状控制中主动杆多目标最优配置

导出自适应桁架结构静态形状控制方程，这些方程在线弹性范围内适用；一般主动杆件数远小于结构杆件数目，且主动杆件的配置问题取决于控制能量和杆件强度等因素，因此基于最短行程和最小导出内力指标和模态退火组合优化算法进行了主动杆件的多目标最优配置；通过算例分析验证了本文分析方法的可行性和有效性。     

Crystallization Behavior of Modified Polyester with Varied Macromolecular Architecture

Several modified polyesters with varied macromolecular architecture, such as branched poly(ethylene terephthalate) (PET) based on glycerol (GL) from 0.004 to 0.05 mol ratio as a branching agent, blocked and branched poly(butylene terephthalate)‐polyether containing poly(tetramethylene oxide) (PTMO) as soft segment and GL as a branching unit, as well as segmented poly(ethylene terephthalate)‐polyether,were prepared. Their crystallization behavior was studied by differential scanning calorimetry (DSC), wide‐angle X‐ray diffraction (WAXD), and polarized optical microscopy (POM). It was found that a small extent of branching may enhance the crystallization of poly(ethylene terephthalate), while high degrees of branching (0.035–0.05) could block the development of crystallization. On the other hand, for even a small extent of incorporation of GL in the more flexible poly(butylene terephthalate)‐polyether chains, no enhanced crystallization was observed; blocking of crystallization from a branching defect may play the main role. The introduction of PTMO in poly(ethylene terephthalate) chains to a small degree facilitated the nucleation and speeded crystallization, but decreased the melting points of the polymers. A small number of nuclei and the greater induction time were found for branched PETs. The spherulities developed in branched PETs were larger and more perfect than those in PET due to less truncation of spherulites resulting from fewer nuclei, whereas the size of spherulities in poly(ethylene terephthalate)‐polyether became smaller with the increase of PTMO.     

Soliton switching in inhomogeneous nonlocal media

We address a simple way to achieve routing of optical spatial solitons via soliton interactions in the inhomogeneous nonlocal media. We reveal that the variation of the nonlocality disturbs the solitons pairs and splits them into two individual solitons which have the same escape angle but opposite deflection directions. In particular, the escape angle monotonically increases with the increase of the nonlocality variation rate. We demonstrate that the soliton pairs could form self-consistent waveguides that are able to controllably guide a weak signal by any output positions.     

Effects of chromophore concentration and film thickness on thermo-optic properties of electro-optic fluorinated polyimide films

Electro-optic (EO) effect and thermo-optic (TO) effect are jointly considered on the basis of field-induced and temperature-affected perturbations of the operating point in waveguide components. TO coefficients of EO fluorinated polyimide films with side-chain azobenzene chromophore were measured by attenuatedtotal-reflection (ATR) technique at different temperatures with TE- and TM-polarized lights, respectively.It is found that the absolute values of TO coefficients increase with the increments of both chromophore concentration and film thickness, but the polarization dependence of TO coefficients increases with the increment of chromophore concentration and decreases with the increment of film thickness.     

Viscometric measurement of the thermodynamics of PAN terpolymer/DMSO/water system and effect of fiber‐forming conditions on the morphology of PAN precursor

The thermodynamics of polyacrylonitrile (PAN) terpolymer/dimethyl sulphoxide (DMSO)/water system was investigated by viscometric method. Fourier transform infrared (FTIR) measurement of the temperature dependence of polymer/solvent interaction was performed in the range of 25–80 °C, which was in good agreement with viscometric results. Meanwhile, the upper critical solution temperature (UCST) for PAN terpolymer/DMSO/water system, which is proved to be stable one, was determined from the temperature dependence of the expansion factor α_η 3 . The morphology of PAN precursor prepared by dry‐jet‐wet spinning with different fiber‐forming conditions was examined with a scanning electron microscope (SEM). Judging from SEM photographs, not only the number and size of microvoids of PAN precursor gradually increase, with increasing the temperature of coagulation bath, but also the cross‐section shape of PAN precursor changes from nephroid shape to elliptical shape or circular shape. Therefore, PAN precursor with different microstructures can be fabricated at different quenching‐depths, suggesting that the final microstructure of the PAN precursor greatly depends on the phase separation in the fiber‐forming process. © 2008 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 46: 1997–2011, 2008