The influence of nucleating agent on crystallization behavior and properties of polypropylene and its copolymer with ethylene

The influences of nucleating agent EDBS on crystallization behavior and properties of polypropylene UP) and its copolymer with a small amount (4. 48 %, molar fraction) of ethylene (CPP) were studied. DSC results indicated that the crystallization temperature of iPP and CPP samples with 0.5 % (mass fraction) EDBS obviously increased and the degree of crystallinity of these samples became higher. In addition, adding small amount of EDBS enhanced the crystallization of the low isotacticity and low molecular weight segments of the CPP. PLM results showed that their spherulite size decreased markedly, and as a result, the transmittance and haze of the films were all improved.

Syntheses and crystal structures of mononuclear rhodium hydrido complexes from the reactions of [Rh(H)(2)(PPh3)(2)(EtOH)(2)]ClO4 with various nitrogen ligands

Reactions of the Rh hydrido complex [Rh(H)(2)(PPh3)(2)(EtOH)(2)]ClO4 (1) With nitrogen ligands such as 2-(4-thiazolyl)benzimidazole (tbz). pyridazine (pdz), imidazole (im) and pyrimidine (pmd) in CH,Cl, afforded Various mononuclear Rh hydrido complexes, [Rh(H)(2)(PPh3)(2)(tbz)]CIO4 (2), [Rh(H)(2)(PPh3)(2)(pdZ)(2)]ClO(4)(.)2CH(2)Cl(2) (3). [Rh(H)Cl(PPh3)(2)(pdz)(2)](ClO4CH2Cl2)-C-. (4). [Rh(H)(2)(PPh3)(2)(im)(2)]ClO(4)(.)2CH(2)Cl(2) (5). [Rh(H)Cl(PPh3)(2)(im)(2)](ClO4CH2Cl2)-C-. (6). [Rh(H)(2)(PPh3)(2)(pmd)(2)](ClO4CH2Cl2)-C-. (7) and the Rh non-hydrido complex [RhCl2(pmd)(4)]ClO4 (8). The Rh complexes 2. 3, 5 and 6 were crystallographically characterized. The formation process was monitored by H-1 NMR and UV-Vis spectra. In all the Rh hydrido complexes, the Rh atom is coordinated by two PPh3. ligands in trans-positions and two nitrogen ligands in the cis-positions. The remaining sites Lire occupied by one or two hydride atoms to form a saturated 18-electron framework in a slightly distorted octahedral geometry. For complex 2 an appreciable inter-molecular pi interaction is observed between planes of tbz and PPh3 ligands, while an intra-molecular hydrogen bonding interaction between C-H and Cl atoms is found in complex 6.

成核剂对聚丙烯及其共聚物的结晶行为和性能的影响

研究了成核剂 1 ,3∶ 2 ,4-对二乙基苄叉山梨醇 (EDBS)对聚丙烯及其乙烯共聚物的结晶行为和结晶形态的影响 ,并对其薄膜进行了光学性能的表征 .结果表明 ,添加少量 (质量分数 0 .5 % )的成核剂 ,使聚丙烯样品的结晶温度大大提高 ,结晶度明显增加 .而对于乙烯共聚聚丙烯样品 ,添加少量 (质量分数 0 .5 % )成核剂 ,不仅使其整体结晶温度大大提高 ,结晶度增加 ,而且明显强化了低有序部分的结晶 .少量成核剂的加入 ,使聚丙烯及其共聚物的球晶尺寸明显缩小 ,薄膜的透光性和雾度显著改善

Monte Carlo simulation for the modification of polymer via grafting

Monte Carlo method has been applied to investigate the kinetic of grafting reaction in free radical copolymerization. The simulation is quits in agreement with that of theoretical and experimental results. It proves that the Monte Carlo simulation is an effective method for investigating the grafting reaction of free radical copolymerization. (C) 2000 Elsevier Science Ltd. All rights reserved.

Catalysis of copper-containing transition metal hydrotalcite-like compounds in the phenol hydroxylation with hydrogen peroxide

Hydrotalcite-like compounds containing carbonate ion as the interlayer anion were prepared by coprecipitation under low supersaturation condition by mixing an aqueous solution of metal nitrates with an aqueous solutions of NaOH and Na2CO3, at room temperature, maintaining pH = 8-10 with vigorous stirring, Following the mixing, the resulting heavy slurry was aged at 353 K for 18 h with vigorous stirring, The precipitate was then filtered, washed several times with hot distilled water and dried in air at 353 K overnight, In this way, CuMI AlCO3-HTLcs and M-I AlCO3-HTLcs were synthesized and characterized by means of XRD and IR, The catalysis of the above mentioned HTLcs were investigated in the phenol hydroxylation with H2O2. The results indicated that all of the copper-containing HTLcs had a higher catalytic activity in the reaction, However, those catalysts that did not contain copper had no catalytic activity in this reaction, This means that copper was the active center in the phenol hydroxylation. Meanwhile, the mechanism was also proposed, which could be used to explain the main reason for higher activity for CuCuAlCO3-HTLcs in the phenol hydroxylation and the effect of Mg2+, Zn2+, Co2+, Ni2+ on activity of CuMI AlCO3-HTLcs.

含铜过渡金属水滑石类化合物对苯酚过氧化氢羟化的催化作用

合成了一系列二元、三元过渡金属水滑石类化合物，并经XRD、IR进行了表征．苯酚过氧化氢羟化结果表明，含铜水滑石类化合物对该反应有较高的催化活性，并初步提出了反应机理.

SEQUENCE-ANALYSIS OF FLUORINE-CONTAINING POLYARYLETHERSULFONE COPOLYMERS BY C-13-NMR

HexafluorobisA polyethersulfone-cardo polyethersulfone, random and block copolymers with different segment lengths were synthesized by a reaction of 4,4'-(hexafluoroisopropylidene)diphenol and 3,3'-bis(4-hydroxyphenyl)-1-isobenzopyrrolidone with bis(4-chl

Global negative vegetation feedback to climate warming responses of leaf litter decomposition rates in cold biomes

Whether climate change will turn cold biomes from large long-term carbon sinks into sources is hotly debated because of the great potential for ecosystem-mediated feedbacks to global climate. Critical are the direction, magnitude and generality of climate responses of plant litter decomposition. Here, we present the first quantitative analysis of the major climate-change-related drivers of litter decomposition rates in cold northern biomes worldwide. Leaf litters collected from the predominant species in 33 global change manipulation experiments in circum-arctic-alpine ecosystems were incubated simultaneously in two contrasting arctic life zones. We demonstrate that longer-term, large-scale changes to leaf litter decomposition will be driven primarily by both direct warming effects and concomitant shifts in plant growth form composition, with a much smaller role for changes in litter quality within species. Specifically, the ongoing warming-induced expansion of shrubs with recalcitrant leaf litter across cold biomes would constitute a negative feedback to global warming. Depending on the strength of other (previously reported) positive feedbacks of shrub expansion on soil carbon turnover, this may partly counteract direct warming enhancement of litter decomposition.

CIMS过程运行管理系统研究

CIMS是将企业主要生产经营活动实现自动化的高度复杂的大规模集成系统;在CIMS的实践过程中,不仅要实现物流和信息流的集成,还要实现组织和功能的集成,进行系统运行过程的有效管理,才能从总体上实现生产的最优调度和控制,从而实现系统最优目标.本文从沈阳鼓风机厂CIMS工程的实际出发,讨论在信息集成的基础上,根据企业内部运行规律对SB-CIMS内的各功能模块进行协调管理,使CIMS内部各功能模块和谐地运行,从而实现功能的集成和系统的最优目标。

未来十年全球无人无缆自主式潜水器的发展趋势

本文阐述了全球无人无缆自主式潜水器（ＡＵＶ）应用背景和重要性，以及它的开发和应用，同时也阐述了中国的开发现状。最后展望未来十年全球无人无缆自主式潜水器（ＡＵＶ）的发展趋势。

太阳辐射对溶解有机质荧光光谱特征的影响

利用三维荧光光谱研究了太阳辐射对溶解有机质(DOM)荧光光谱特征的影响。实验结果表明,太阳辐射使DOM的荧光发射光谱强度减弱。在三维荧光光谱图中,红枫湖样品的荧光峰A,C,南明河样品的荧光峰A,B,C,尤其是荧光峰C的λExmax/λEmmax位置随着太阳辐射时间的延长而逐渐向短波长移动。从腐殖酸样品的三维荧光光谱图中则发现,原始样品荧光峰位置出现在λEx/λEm=275/500nm处,光照作用后出现两个荧光峰λEx/λEm=245/450nm和310/450nm。太阳辐射对DOM中不同荧光组分的光降解速率存在差异,从荧光峰A和C的比值r(A,C)随太阳辐射时间的变化趋势得知,荧光峰C比荧光

桂中旱片的成因机制及早片综合区划

桂中地区降水不少,但由于自然及人为等因素,旱情严重,成为广西著名的旱片之一。对其成因机制的探讨是桂中环境治理和区域开发的科学基础。在概述地质地理特征的基础上,进行了桂中旱区的干旱时空分析,重点揭示了桂中旱片的成因机制;然后,根据干旱类型、旱灾脆弱度及从便于地下水利用出发,进行了桂中旱片的综合区划;最后,遵循生态环境治理、综合抗旱与脱贫致富相结合的原则,提出了治理对策措施。