自适应混合多目标分布估计进化算法

针对多目标分布估计算法全局收敛性较弱的缺陷,提出了一种自适应混合多目标分布估计进化算法。其基本思想是:在多目标分布估计算法中引入全局收敛性较强的差分进化算法,当函数变化率较大时,用分布估计算法产生新种群;当函数变化率较小即算法可能陷入局部收敛时,用差分进化算法产生新种群。理论分析和数值实验结果表明,这种混合算法不仅具有良好的全局收敛性,而且解的分布性和均匀性较没有考虑目标函数变化率的混合多目标分布估计算法也有了一定程度的提高。     

半封闭连通管式差压传感器在桥梁挠度测量中的应用

挠度是评价桥梁结构安全性的重要指标。根据桥梁结构特点,选用半封闭连通管式差压传感器进行实际工程应用。论述了传感器的基本原理,介绍了实际的半封闭连通管式差压传感器及其系统的构成,并将该传感系统应用于荆岳长江公路大桥通车鉴定试验的静载挠度测量中,测量结果表明:半封闭连通管式差压传感器的测量数据能够有效地反映桥梁结构状态变化,且具有较高的测量效率和准确度。     

医用内窥镜微型摄像模组设计

设计了一种新型医用内窥镜微型摄像模组.该模组采用微型、高分辨率的CMOS图像传感器结合低压差分信号（LVDS）传输技术进行设计,使摄像模组直径缩减至5.0mm,并实现了图像数据的长距离高保真传输.搭建了实验平台对摄像模组的摄像功能进行了测试.结果表明：该模组图像传输距离超过2m,分辨率达到30万像素,对口腔溃疡模拟粘膜病变的识别率高达90％.其图像分辨率高,传输距离长,使其适用于内镜诊断;其直径小,能大大提高病人内镜检查的舒适性,为超细内镜诊断提供了一种极佳的解决方案.     

钒钼酸铵分光光度法快速测定磷酸二铵中有效五氧化二磷

为了快速测定磷铵中P2O5含量,将0.1mol/LEDTA预热至80±2℃作为DAP有效P2O5的提取液,提取时间25min以上。鉴于正磷酸根在酸性介质中与钼酸盐及偏钒酸盐生成稳定的黄色化合物,在400nm波长下,利用示差法测定P2O5仅需50～55min。该方法的相对标准偏差(RSD)为0.13%～0.28%,回收率99.1%～101.1%,精密度和准确度好。     

Competitive removal of Pb2+, Cd2+, and Zn2+ by poly(acrylamide‐co‐maleic acid) hydrogels/differential pulse polarographic determination

Poly(acrylamide‐co‐maleic acid) [P(AAm/MA)] hydrogels, with various compositions, were prepared from ternary mixtures of acrylamide (AAm)/maleic acid (MA)/water by using ⁶⁰Co γ‐rays. The effect of composition of these hydrogels, on the competitive removal of Pb²⁺, Cd²⁺, and Zn²⁺ ions from aqueous solution, was investigated. The hydrogel compositions and their adsorption behaviors were determined by use of differential pulse polarography, a very sensitive electroanalytical technique. It was observed that the external stimuli of pH, temperature, and ionic strength have an important role on the adsorption. The increments of MA content in P(AAm/MA) hydrogels caused a significant increase in the adsorption these ions. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2401–2406, 2004     

Crystallization kinetics of low‐density polyethylene and polypropylene melt‐blended with a low‐Tg tin‐based phosphate glass

The nonisothermal and isothermal crystallizations of low‐density polyethylene (LDPE) and polypropylene (PP) in phosphate glass (Pglass)–polymer hybrid blends were studied through differential scanning calorimetry (DSC). As the Pglass volume fraction was increased, the percentage crystallinity decreased. The half‐time for crystallization decreased as the propagation rate constant rose, for both of the polymer matrices, with increasing Pglass concentrations. The Pglass was observed to be a nucleating agent for formation of two‐ or three‐dimensional spherulites in the hybrids. Tensile modulus improved for both of the Pglass–polymer hybrids up to 40% Pglass, but the energy to break decreased. Tensile strength changed slightly with the addition of Pglass to the LDPE matrix, exhibiting a larger value than that of pure LDPE at 30%. The tensile strength decreased as more Pglass was added to the PP matrix. The observed differences between tensile properties of the Pglass–PP and Pglass–LDPE hybrids at identical Pglass volume concentration were found to be consistent with that of the crystallization behavior of the hybrids. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3445–3456, 2003     

Kinetic study of radical polymerization. II. Solid‐state bulk polymerization of sodium methacrylate by differential scanning calorimetry

The solid‐state radical polymerization of sodium methacrylate was investigated. It was initiated by azobisisobutyronitrile, which was used as a radical initiator. Differential scanning calorimetry (DSC) was used to observe the endothermic and exothermic transitions during the polymerization reaction. Structural studies were performed with the DSC thermograms and Fourier transform infrared and ultraviolet–visible spectra, and all of the results confirmed the progress of the reaction. The obtained data revealed that the polymerization reaction proceeded completely with a 100% conversion. ΔH of this reaction was calculated with various amounts of the initiator, and the peak temperatures were determined at different heating rates. The activation energy (19.7 kcal mol^?1) was also obtained by the Kissinger method for this type of solid polymerization reaction. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1648–1654, 2003     

基于祖冲之类方法的多体动力学方程保能量保约束积分

针对一类多体动力学问题导出的微分 代数方程,提出一种保能量、保约束的算法.该算法基于祖冲之类方法和欧拉中点保辛差分,利用祖冲之类方法保证在时间格点上精确满足约束方程,避免约束违约问题;并进一步证明该算法在时间格点上可以精确保能量.数值算例进一步验证该算法的可靠性.     

Cold Crystallization of PLLA Studied by Simultaneous SAXS and WAXS

Summary: The cold crystallization process of initially amorphous poly(L ‐lactic acid), PLLA, with two different molecular weights, during a heating at 2 °C/min, was investigated by DSC and time‐resolved simultaneous SAXS and WAXS, using synchrotron radiation. Equatorial scans of the isotropic 2D‐SAXS patterns showed that the average Bragg long period (L_B) of PLLA samples was approximately constant with the development of cold crystallization up to a temperature that corresponded to a melt/re‐crystallization process that took place before the nominal melting peak seen by DSC. L_B values were found to be higher for the high molecular weight material. This was in accordance with the higher melting temperature observed in the high molecular weight PLLA that implied the existence of thicker lamellae. WAXS results showed that the molecular weight did not apparently affect the crystal form and the final degree of crystallinity of PLLA. The Avrami parameters from WAXS and DSC were consistent, showing that the non‐isothermal cold crystallization of the two PLLA samples corresponded mainly to a three‐dimensional growth, although an imperfect crystallization process was involved at early times. The crystallization rate of PLLA, observed both by WAXS and DSC, decreased with increasing molecular weight.

SAXS profiles of PLLA2 as a function of temperature. The inset shows the 2D‐SAXS pattern obtained at 180 °C.     

Synthesis of copolymers of tert‐butyl vinyl ether with maleic and citraconic anhydrides

In the present study, the effects of charge‐transfer complex formation and intramolecular fragmentation (side‐chain lactonization) in radical copolymerization of tert‐butyl vinyl ether (t‐BVE) with anhydrides of maleic (MA) and citraconic (CA) acids and the structure–thermal behavior relationships of the resulting copolymers were examined using the ¹H‐NMR, FTIR, DSC, and TGA analysis methods. It was shown that copolymerization under the chosen conditions proceeded through intramolecular fragmentation with the formation of γ‐lactone units. Side‐chain fragmentation of t‐BVE–MA and t‐BVE–CA copolymers also was confirmed by TGA and DSC analysis. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2455–2463, 2006 2006