Brittle-ductile transition in high-density polyethylene/glass-bead blends: Effects of interparticle distance and temperature

The toughness of high-density polyethylene (HDPE)/glass-bead blends containing various glass-bead contents as a function of temperature was studied. The toughness of the blends was determined from the notch Izod impact test. A sharp brittle-ductile transition was observed in impact strength-interparticle distance (ID) curves at various temperatures. The brittle-ductile transition of HDPE/glass-bead blends occurred either with reduced ID or with increased temperature. The results indicated that the brittle-ductile-transition temperature dropped markedly with increasing glass-bead content. Moreover, the correlation between the critical interparticle distance (ID.) and temperature was obtained. Similar to the ID, of polymer blends with elastomers, the ID, nonlinearly increased with increasing temperature. However, this was the first observation of the variation of the ID, with temperature for polymer blends with rigid particles. (C) 2001 John Wiley & Sons, Inc. J Polym. Sci Part B: Polym. Phys 39: 1855-1859, 2001.

Gas permeation properties of cardo polyaryletherketones containing different alkyl substituents

The gas permeation properties of a series of cardo polyaryletherketone materials are reported, In this series, the hydrogen atoms of benzene rings on the backbone are systematically replaced with different alkyl substituents. The effects of temperature and structure variation on gas permeability and selectivity are discussed in detail. The experimental results revealed that the polyetherketone obtained by the introduction of dimethyl and diisopropyl substituents to phenolphthalein unit is 3 similar to 6 times more permeable than the unmodified one for the gases studied.

Structure of hydrated dysprosium picolinate, [Dy(C5H4NCO2)(3)(H2O)(2)]2.8H(2)O

The crystal structure of the title compound was determined by X-ray diffraction. The dysprosium ion is eight-coordinated by three oxygen atoms and three nitrogen atoms from three picolinato ions and two water oxygen atoms. The nitrogen atom and one carboxyl oxygen atom of each picolinato ion are coordinated to the same dysprosium ion to form a five-membered chelating ring. The title compound exists as discrete molecules in the crystal structure.

含不同取代基的Cardo聚芳醚酮的气体透过性能

研究了带有不同烷基取代基的Ｃａｒｄｏ聚芳醚酮均质膜对Ｈ２、Ｏ２、Ｎ２、ＣＯ２和ＣＨ４气体的透气性能，讨论了气体透过对温度的依赖性。与未改性酚酞聚芳醚酮相比，在主链苯环上引入异丙基侧基会使气体透过系数提高３～６倍；每个结构单元苯环被４个甲基取代后，气体透过系数和选择分离系数同时得到较大改善，其中Ｈ２的透过系数为２２ｂａｒｒｅｒ，Ｈ２／Ｎ２分离系数为１１４。

ELECTROCHEMICAL STUDY OF ISOPOLY-OXOMETALLATE AND HETEROPOLY-OXOMETALLATE FILM MODIFIED MICROELECTRODES .2. ELECTROCHEMICAL-BEHAVIOR OF ISOPOLYMOLYBDIC ACID MONOLAYER MODIFIED CARBON-FIBER MICROELECTRODES

In this paper the electrochemical properties of isopolymolybdic anion thin film modified carbon fibre (CF) microelectrode prepared by simple dip coating have been described. The modified electrode shows three couples of surface redox waves between + 0.70 and - 0.1 V vs. sce in 2 M H2SO4 solution with good stability and reversibility. The pH of solution has a marked effect on the electrochemical behaviour and stability of the film, the stronger the acidity of electrolyte solution is, the better the stability and reversibility of isopolymolybdic anion film CF microelectrode will be. The scanning potential range strongly influences on the electrochemical behaviour of the film. The isopolymolybdic anion film prepared by the dip coating resulting a monolayer with estimated surface concentration (F) 2.8 x 10(-11) mol cm-2. From the half-peak widths and peak areas of the surface redox waves of the film electrode, the first three surface waves are corresponding to two-electron processes. The electron energy spectra show the products by six electrons reduction are a mixture of Mo(VI) and Mo(V) species. The electrochemical reaction of the isopolymolybdic anion monolayer can be expressed as Mo8O264- + mH+ + 2ne half arrow right over half arrow left [HmMo8-2n(VI)Mo2n(V)O26](4,2n-m)-n = 1, 2, 3; m = 2, 5, 7.

Seasonal and interannual variability of primary and export production in the South China Sea: a three-dimensional physical-biogeochemical model study

To investigate the seasonal and interannual variations in biological productivity in the South China Sea (SCS), a Pacific basin-wide physical - biogeochemical model has been developed and used to estimate the biological productivity and export flux in the SCS. The Pacific circulation model, based on the Regional Ocean Model Systems (ROMS), is forced with daily air-sea fluxes derived from the NCEP (National Centers for Environmental Prediction) reanalysis between 1990 and 2004. The biogeochemical processes are simulated with a carbon, Si(OH)(4), and nitrogen ecosystem (CoSiNE) model consisting of silicate, nitrate, ammonium, two phytoplankton groups (small phytoplankton and large phytoplankton), two zooplankton grazers (small micrograzers and large mesozooplankton), and two detritus pools. The ROMS-CoSiNE model favourably reproduces many of the observed features, such as ChI a, nutrients, and primary production (PP) in the SCS. The modelled depth-integrated PP over the euphotic zone (0-125 m) varies seasonally, with the highest value of 386 mg C m (-2) d (-1) during winter and the lowest value of 156 mg C m (-2) d (-1) during early summer. The annual mean value is 196 mg C m (-2) d (-1). The model-integrated annual mean new production (uptake of nitrate), in carbon units, is 64.4 mg C m (-2) d (-1) which yields an f-ratio of 0.33 for the entire SCS. The modelled export ratio (e-ratio: the ratio of export to PP) is 0.24 for the basin-wide SCS. The year-to-year variation of biological productivity in the SCS is weaker than the seasonal variation. The large phytoplankton group tends to dominate over the smaller phytoplankton group, and likely plays an important role in determining the interannual variability of primary and new production.

Bromophenols coupled with methyl gamma-ureidobutyrate and bromophenol sulfates from the red alga Rhodomela confervoides

Four new bromophenols C-N coupled with methyl gamma-ureidobutyrate (1-4), a phenylethanol bromophenol (5), and three phenylethanol sulfate bromophenols (6-8) have been isolated from polar fractions of an ethanolic extract of the red alga Rhodomela confervoides. On the basis of spectroscopic evidence including HRMS and 2D NMR data, the structures of the new compounds were determined as methyl N'-(2,3-dibromo-4,5-dihydroxybenzyl)-gamma-ureidobutyrate (1), methyl N,N'-bis(2,3-dibromo-4,5-dihydroxybenzyl)-gamma-ureidobutyrate (2), methyl N'-[3-bromo-2-(2,3-dibromo-4,5-dihydroxybenzyl)-4,5-dihydroxybenzyl]-gamma-ureidobutyrate (3), methyl N'-(2,3-dibromo-4,5-dihydroxybenzyl)-A7-[3-bromo2-(2,3-dibromo-4,5-dihydroxybenzyl)-4,5-dihydroxybenzyl]-gamma-ureidobutyrate (4), 2,3-dibromo-4,5-dihydroxyphenylethanol (5), 2,3-dibromo-4,5-dihydroxyphenylethanol Sulfate (6), 3-bromo-4,5-dihydroxyphenylethanol sulfate (7), and 3-bromo2-(2,3-dibromo-4,5-dihydroxybenzyl)-4,5-dihydroxyphenylethanol sulfate (8). The cytotoxicity of all compounds was evaluated against several human cancer cell lines including human colon cancer (HCT-8), hepatoma (Bel7402), stomach cancer (BGC-823), lung adenocarcinoma (A549), and human ovarian cancer (A2780). Among them, the phenylethanol and the phenylethanol sulfate bromophenols (5-8) showed moderate cytotoxicity against all tested cell lines.

高寒湿地生态系统土壤有机物质补给及地-气CO_2交换特征

海北高寒湿地植物地上、地下生物现存量较高，2004年海北高寒湿地植物净初级生产力为1799．7gC•m~(-2)．由于家畜对湿地植物采食量低，每年将有大量的枯黄植物残留于地表，表现出地上、地下生物量以及苔鲜均成为土壤有机物质的补给源．由于区域温度低，积水严重，对植物残体分解缓慢，导致湿地土壤有机质含量很高，形成了厚达2m左右的泥炭层．观测结果表明，海北高寒湿地净生态系统CO_2交换量具有明显的季节变化，年内4月和10月存在两个CO_2释放高峰期，夏季的7～8月为一个强吸收期，全年来看为一个巨大的碳源．2004年净生态系统年碳交换量为76．7gC•m~(-2)．计算结果表明，植被的呼吸消耗量每年为1199．8gC•m~(-2)，其植物总固碳量为2999．5gC•m~(-2)，而土壤呼吸为1876．4gC•m~(-2)．

图像图形文字混合处理系统PANDA的设计与实现

本文描述了图像、图形、文字混合处理系统PANDA的设计与实现技术。详细讨论了PANDA系统的数据结构组织方法,其中包括多文件、多窗口处理的结构设计以及动态的数据结构设计,同时给出了PANDA系统在其实现过程中所使用的一些关键处理技术。

智能机器人基于作业子空间划分的自学习自适应控制方法

现有的机器人自适应控制基本上都是在建立机器人线性化的动力学模型的基础上,采用某种显式或隐式参数辨识的方法,在线地修正控制作用.本文针对机器人运动和动力学参数变化的固有特点,提出一种完全不同的自学习自适应方法.这种方法基于智能机器人分级系统中的两级结构,并且在空间域里而不是在时间域里处理机器人参数的变化.把机器人的作业空间划分成子空间,其中包括重力载荷的作用,每个子空间对应一组控制器.规划的轨迹映射到作业空间形成子空间序列.用自学习方法选择与这个序列对应的最佳控制器序列.该方法算法简单,计算量小.避开了通常的自适应方法遇到的一系列困难问题.

胡敏酸的结构特征及其吸附行为

使用0. 5 mol/L NaOH和0. 1 mol/L Na4 P2O7 溶液分别从土壤中提取胡敏酸,并且对其进行了元素分析、红外光谱、固态13C核磁共振的定性、定量研究。结果表明,两种胡敏酸的性质很相似,但也存在一些微小差异,Na4 P2O7 提取的胡敏酸比NaOH提取的具有芳香度较大、聚合度较高、极性官能团含量较多的特点。测定了菲在6个胡敏酸上的吸附等温线, Freundlich模型很好的拟合了所有吸附等温线,相关系数r均在0. 992以上。有机碳分配系数Koc与胡敏酸中极性碳(POC)之间存在明显的线性相关关系,并受到提取剂类型的影响。

(古)盐度研究的一种重要工具——锶同位素

本文详细地阐述了海水－陆表水双元体系中锶同位素的混合原理、混合水体中＾８７Ｓｒ／＾８６Ｓｒ值与盐度的定量关系。利用Ｓｒ同位素不随生物、何尝作用过程发生分馏作用及Ｓｒ与Ｃａ化学性质相似等特征，地层、沉积物中生物壳体和碳酸盐岩＾８７Ｓｒ／＾８６Ｓｒ值可作为沉积水体（古）盐度确定的一种有用工具。文中详细地综述了国内外在这方面的研究进展，并讨论了成岩后生作用对生物壳体和碳酸盐岩＾８７Ｓｒ／＾８６Ｓｒ原始值

An in-situ modified sol-gel process for monolith catalyst preparation used in the partial oxidation of methane

An in-situ modified sol-gel method for the preparation of a Ni-based monolith-supported catalyst is reported. With the presence of a proper amount of plasticizer and binder, and at an optimized pH value, the stable boehmite sol was modified with metal ions (Ni, Li, La) successfully without distinct growth of the particle size. Monolith-supported Ni-based/gamma-Al2O3 catalysts were obtained using the modified sol as the coating medium with several cycles of dip-coating and calcination. Combined BET, SEM-EDS, XRD and H-2-TPR investigations demonstrated that the derived monolith catalysts had a high specific surface area, a relatively homogeneous surface composition, and a high extent of interaction between the active component and the support. These catalysts showed relatively stable catalytic activities for partial oxidation of methane (POM) to syngas under atmospheric pressure. The monolith catalysts prepared by this sol-gel method also demonstrated an improved resistance to sintering and loss of the active component during the reaction process.