非晶有机锆聚合物的制备及光催化CO2合成甲醇

采用溶剂热法在增透的多孔玻璃表面制备负载非晶态有机锆聚合物。通过SEM，XRD，BET，FTIR，UV-Vis，ICP，有机元素分析，荧光光谱（PL）及紫外光电子能谱（UPS ）等手段对催化剂进行了测试分析。非晶态有机锆聚合物（2.64 eV）具有比NH2-UiO-66(Zr)（2.74 eV）更窄的禁带宽度，更稳定的光生电子。在光催化反应器中放入2片负载非晶态有机锆的玻璃（总面积50.4 cm2），在300 W的氙灯照射下催化还原CO2合成甲醇，反应4 h后甲醇的产量为443.0 μmol，转换频率（TOF）为8.9 h-1。当0.1 g NH2-UiO-66(Zr)为催化剂时，甲醇的产量为244.3 μmol，TOF仅为0.17 h-1。非晶有机锆聚合物的光催化性能明显优于NH2-UiO-66(Zr)粉末，且循环稳定性良好。     

骑式摩托车油箱喷涂工艺的改进

面对日益激烈的市场竞争,摩托车油箱外观质量越来越成为影响销售的因素之一。文章介绍了改进工艺后的油箱涂装,该涂装体系提高了油箱外观的丰满度,降低了油箱涂装的生产成本。     

WG-800离心机异常振动问题的解决

分析了引起WG-800离心机异常振动的原因,采用自制的实心橡胶减震器并采取一些预防振动措施后,离心机的振幅在正常范围之内,取得了较好的效果。     

新型高耐蚀车辆保护蜡的研究

研制了一种耐蚀性能要求较高环境下使用的车辆保护蜡，采用高分子树脂，防锈添加剂与蜡膜相结合的方法，大幅提高了耐蚀性等质量性能，满足了厂家和用户的要求，成功应用于车辆的涂装。     

基于几何特征的流体动画控制方法

在流体动画中,流体控制是生成可控流体运动的关键技术.为产生视觉逼真、行为可控的流体动画效果,提出一种基于几何特征的流体控制方法.首先通过构建流体形状的时变几何分区,实现对可控流体形状的表达及动态跟踪;在此基础上设计异构控制模型,以增强流体运动控制的灵活性,该模型采用了带约束优化的刚性控制和基于弹簧模型的柔性控制2种方法;最后将异构控制模型与高精度流体物理模型相耦合,生成视觉逼真的可控流体运动效果.实验结果表明,该方法能够在保持流体角色形状的同时产生丰富的流体细节,满足动画师的设计需求.     

(NH4)2SO4-CuSO4-CTMAB-湿法磷酸体系浮选分离碘(I-)的研究

研究了硫酸铵-硫酸铜-十六烷基三甲基溴化铵-湿法磷酸体系浮选碘(I-)的行为及其与常见离子分离的条件。试验表明,在1.0g(NH4)2SO4存在下,体系中硫酸铜和十六烷基三甲基溴化铵(CTMAB)的用量分别为(2.4×10-2mol/L)0.5ml和0.025g,I-与Cu(Ⅱ)形成的CuI沉淀能被CTMAB浮选,而其它非金属离子不被浮选,从而实现碘(I-)与这些离子之间的定量分离。本法对湿法磷酸中微量碘进行了定量浮选分离,结果满意。     

Preparation and characterization of a PMMA/Ce(OH)3, Pr2O3/graphite nanosheet composite

An easy process for the synthesis of poly(methyl methacrylate)/Ce(OH)₃, Pr₂O₃/graphite nanosheet (PMMA/Ce(OH)₃, Pr₂O₃/NanoG) composite was developed. Graphite nanosheets (NanoG) were prepared by treating the expanded graphite with sonication in aqueous alcohol solution. The PMMA/Ce(OH)₃, Pr₂O₃/NanoG composites were prepared via in situ polymerization of MMA monomer in the presence of graphite nanosheets and Ce(OH)₃, Pr₂O₃ through reverse micelle template, in which the methyl methacrylate was designated as the oily phase. The composites were then dispersed with chloroform and coated on glass slides to form films. Scanning and transmission electron microscopy were used to characterize the structure and dispersion of the graphite nanosheets and the composites. The results showed that the high-aspect-ratio structure of the nanosheets played an important role in forming a conducting network in the PMMA matrix. From thermogravimetric analysis, the introduction of graphite nanosheets and inorganic nanopartices exhibited a beneficial effect on the thermal stability of PMMA.     

Synthesis and luminescence properties of new blue‐light‐emitting polyconjugated poly{1,1′‐biphenyl‐4,4′‐diyl‐[1‐(4‐t‐butylphenyl)]vinylene} polymers and copolymers

Three new soluble polyconjugated polymers, all of which emitted blue light in photoluminescence and electroluminescence, were synthesized, and their luminescence properties were studied. The polymers were poly{1,1′‐biphenyl‐4,4′‐diyl‐[1‐(4‐t‐butylphenyl)]vinylene}, poly((9,9‐dioctylfluorene‐2,7‐diyl)‐alt‐{1,4‐phenylene‐[1‐(4‐t‐butylphenyl)vinylene‐1,4‐phenylene]}) [P(DOF‐PVP)], and poly([N‐(2‐ethyl) hexylcarbazole‐3,6‐diyl]‐alt‐{1,4‐phenylene‐[1‐(4‐t‐butylphenyl)]vinylene‐1,4‐phenylene}). The last two polymers had alternating sequences of the two structural units. Among the three polymers, P(DOF‐PVP) performed best in the light‐emitting diode devices of indium–tin oxide/poly(ethylenedioxythiophene) doped with poly(styrene sulfonate) (30 nm)/polymer (150 nm)/Li:Al (100 nm). This might have been correlated with the balance in and magnitude of the mobility of the charge carriers, that is, positive holes and electrons, and also the electronic structure, that is, highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) levels, of the polymers. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 307–317, 2006     

秋季太湖叶绿素a浓度荧光反演研究

基于2007年11~12月太湖全湖实测水质参数和光谱数据,首先利用高斯方程对遥感反射率进行过滤分解,找出叶绿素a(chl\|a)吸收峰675 nm以后的荧光反射峰(Fluorescence Peak:FP),再以662 nm处的反射率为基准,采用归一化荧光高度法进行叶绿素a浓度(C chl-a)反演,得到chl-a反演模型。基于高斯分解获取的chl-a的荧光反射峰值R(FP)与662 nm处的反射率R (662)比值［R(FP)/R(662)］与C chl-a之间存在显著的相关性,该模型为秋季太湖水体C chl-a的最佳反演模型。在高悬浮泥沙条件下,该模型能够较好地表示出叶绿素荧光高度与叶绿素浓度之间的关系,为C chl-a反演提供新的方法和依据,并为传感器敏感波段的选取和设置提供参考。     

Effect of time/temperature treatment parameters on depolymerization of chitosan

Depolymerization of the biopolymer chitosan by an autoclaving process at 121°C and 15 psi was investigated using various treatments. Acetic acid was found to be the most effective solvent in decreasing chitosan viscosity among the six organic acids tested. The rate of viscosity decrease increased with increasing chitosan concentration. The viscosity of 1% chitosan in 1% acetic acid decreased rapidly to 91% of the initial viscosity following the initial 15 min of autoclaving. This decreased gradually to 93% and 94% in 30 and 60 min, respectively, without being adversely affected by the chitosan solution volume. The degree of deacetylation was comparable before and after autoclaving for 60 min. Chitosan at three molecular weights (M_r = 1597, 1110, and 789 kDa) decreased in molecular weight by 46%–51% in the 15‐min treatment, 55%–60% in the 30‐min treatment, and 60%–62% in the 60‐min treatment. The addition of 0.1%–1.0% (v/v) concentrations of hydrogen peroxide to the chitosan solution autoclaved for 15 min decreased viscosity by 94%–98% and molecular weight by 69%–83%. This process is a simple, timesaving, homogeneous depolymerization procedure, and it is possible to prepare partially hydrolyzed chitosan with specified molecular weights by regulating the time of treatment. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1890–1894, 2003