含甲基丙烯酸叔丁酯单元聚合物的合成及其酸解性能研究

本研究合成了甲基丙烯酸叔丁酯(TBMA)单体及其均聚物,并与甲基丙烯酸(MAA)共聚合成了二元共聚物。同时以对甲苯磺酸作为酸源,比较系统地研究了聚合物中甲基丙烯酸叔丁酯单元的酸姐情况及其影响因素。研究表明,酸含量的增加和烤版温度的适当升高对甲基丙烯酸叔丁酯单元的酸解有利,烤版时间对甲基丙烯酸叔丁酯单元的酸解比例有一定影响。     

过氧化氢在生成戊二酰-7-氨基头孢烷酸过程中的影响

头孢菌素C(CPC)在D-氨基酸氧化酶为催化剂的情况下,与O2反应生成α-ketoadipyl-7-ACA,再与过氧化氢反应生成戊二酰基-7-氨基头孢烷酸(Gl-7-ACA).在此反应中生成的α-ketoadipyl-7-ACA是造成目标产物收率低的关键因素之一.通过加入适量的双氧水可以使剩余的α-ketoadipl-7-ACA转化为Gl-7-ACA,从而使裂解的收率提高5%.     

Prediction-based realistic 3D model compression

The benefit of using the geometry image to represent an arbitrary 3D mesh is that the 3D mesh can be re-sampled as a completely regular structure and coded efficiently by common image compression methods. For geometry image-based 3D mesh compression, we need to code the normal-map images while coding geometry images to improve the subjective quality and realistic effects of the reconstructed model. In traditional methods, a geometry image and a normal-map image are coded independently. However a strong correlation exists between these two kinds of images, because both of them are generated from the same 3D mesh and share the same parameterization. In this paper we propose a predictive coding framework, in which the normal-map image is predicted based on the geometric correlation between them. Additionally we utilize the strong geometric correlation among three components of normal-map image to improve the predicting accuracy. The experimental results show the proposed coding framework improves the coding efficiency of normal-map image, meanwhile the realistic effect of a 3D mesh is significantly enhanced.     

基于无线传感器网络的水质监测系统设计

使用传统的有线水质监测系统进行水环境污染检测时,存在监测点数量多、监测时间长等问题。为此,提出一种基于无线传感器网络的水质监测系统。通过无线传感器节点对被监测水域进行水质参数的数据采集,将采集到的数据经过Zigbee网络进行汇总及处理,并经过GPRS网络及时地远程传送给监管部门,从而实现对河流水质情况的实时、有效的监督和管理。对水质监测系统的软硬件电路设计进行介绍,并实现对系统的软硬件连调。实验结果证明,该系统能够满足组网要求,可较好地应用于水质监测领域。     

基于分辨函数的极大团搜索算法

寻找极大团是几何图论极为重要的基础研究问题之一。将分辨函数模型与极大团性质结合,定义了顶点的极大团分辨函数、顶点关于某顶点子集的布尔映射函数,得到了一些与极大团相关的重要性质与定理,证明了图的极大团搜索问题可快捷自然地转换为相对简单的分辨函数表达式约束,为设计极大团搜索算法提供了一种有效的理论依据与求解途径。进而引入约简树构造方法设计了基于分辨函数的极大团搜索算法,最后通过给定无向连通图实例说明了算法的可行性与有效性。     

Preparation and characterization of modified starch‐based plastic film reinforced with short pulp fiber. II. Mechanical properties

Native corn starch‐ and hydroxypropylated starch (HPS‐) based plastic films were prepared using the short pulp fiber as the reinforcement and the glycerol as the plasticizer. The results of tensile test showed that the strain and stress at break and elastic modulus increased with pulp content. With glycerol content, the strain at break increased considerably, but the breaking stress and elastic modulus decreased. And the stress–strain curves showed that the brittleness problem of films was overcome by the pulp, glycerol, and water content. The hydroxypropyl starch films showed results similar to those of the native starch films. The results of the three‐point bending test showed that maximum deflection, flexural strength, and specific work increased with pulp content, but the flexural modulus was the highest at a pulp content of 20%. And with the glycerol content, the maximum deflection and specific work of rupture increased, but the bending elastic modulus decreased. The hydroxypropyl starch films showed results similar to those of native starch films as far as the maximum deflection and flexural strength were concerned, but the bending elastic modulus and specific work of the hydroxypropyl starch films were considerably lower than those of starch films. So it was concluded that the flexibility of films was improved by the hydroxypropylation. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2108–2117, 2003     

Controllable Fabrication of Co3−xMnxO4 with Tunable External Co3+/Co2+ Ratio for Promoted Oxygen Reduction Reaction

Co_3?xMn_xO₄ is a bimetal oxide with excellent electrochemical activity in alkaline solution, has been regarded as a promising alternative in the field of ion-air batteries and proton exchange membrane fuel cell (PEMFC). Herein, we report a simple solvothermal-calcination method to fabricate Co_3?xMn_xO₄ with tunable external Co³⁺/Co²⁺ and Mn³⁺/Mn²⁺ ratio. The tunable ratio of element valence in the bimetal results in a higher exposure of active center for oxygen redox reaction (ORR), and thus lead to a better ORR activity, which was confirmed by X-ray photoelectron spectroscopy characterizations and electrochemical measurements. Specially, Co_1.8Mn_1.2O₄ with a Co³⁺/Co²⁺ ratio of 2.08 showed an overpotential of 0.37 V at benchmark ORR current density of 3 mA/cm² in 0.1 M KOH, which is lower than that of pure oxide (Mn₃O₄ 0.53 V and Co3O4 0.56 V). In addition, the as prepared Co_1.8Mn_1.2O₄ exhibited a positive half-wave potential (0.83 V vs RHE) due to their more active sites, promotes charge transfer, adsorption and desorption of oxygen species. This work provides a strategy for the design and fabrication of earth-abundant, low-cost electrocatalysts for PEMFC in practical applications.

Graphic Abstract

Co_3?xMn_xO₄ was fabricated by tuning external Co³⁺/Co²⁺ and Mn³⁺/Mn²⁺ ratio, and the activity initially shows a positive correlation with the ration of Co³⁺/Co²⁺ in Co_3?xMn_xO₄.

     

Epitaxy growth and directed crystallization of high-density polyethylene in the oriented blends with isotactic polypropylene

Various lamellar orientations of high-density polyethylene (HDPE), due to competition between bulk nucleation and interfacial nucleation, have been realized in its melt drawn blends with isotactic polypropylene (iPP) upon cooling after subjected to 160 °C for 30 min. Directed crystallization, with heterogeneous nucleation in the bulk (within domains), is defined as lamellar growth along boundary of anisotropic domains and is favored in larger domains at higher temperature (slow cooling), since overgrowth of lamellae can feel the interface rather than impingement with neighbor ones as a result of scare nuclei at higher temperature. Moreover, lamellar growth caused by directed crystallization is dependent of dimension of confinement. Due to 2D confinement of cylindrical domains, lamellae can only grow along the axis of cylinder and thus b-axis orientation is formed. While in the layered domains with 1D confinement, however, lamellae grow with the normal of (110) plane along the melt drawn direction. On the other hand, epitaxial growth of HDPE chains onto iPP lamellae is related to the surface-induced crystallization and dominated by the interfacial nucleation. Only interfacial nucleation is preferred can epitaxial growth occur. Therefore, retarded crystallization, realized by either strong confinement in finer domains or rapid cooling or both, is favorable for it.     

Influence of polymerization conditions on the structure and properties of polyethylene/polypropylene in‐reactor alloy synthesized in the gas phase with a spherical Ziegler–Natta catalyst

A spherical TiCl₄/MgCl₂‐based catalyst was used in the synthesis of in‐reactor polyethylene/polypropylene alloys by polyethylene homopolymerization and subsequent homopolymerization of propylene in the gas phase. Different conditions in the ethylene homopolymerization stage, such as monomer pressure and polymerization temperature, were investigated, and their influences on the structure and properties of in‐reactor alloys were studied. Raising the polymerization temperature is the most effective way of speeding up polymerization and regulating the ethylene content of polyethylene (PE)/polypropylene (PP) alloys, but it will cause a greater increase in the PE‐b‐PP block copolymer fraction (named fraction D) than in the fraction of PP‐block‐PE in which the PP segments have low or medium isotacticity (named fraction A). Although changing ethylene monomer pressure could influence the ethylene content of PE/PP alloys slightly, it is an effective way of regulating the structural distribution. Reducing the monomer pressure will evidently increase fractions A and D. The mechanical properties of the alloys, including impact strength and flexural modulus, can be regulated in a broad range with changes in polymerization conditions. These properties are highly dependent on the amount, distribution, and chain structure of fractions A and D. The impact strength is affected by both fraction A and fraction D in a complicated way, whereas the flexural modulus is mainly determined by the amount of fraction A. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2136–2143, 2006     

Graft copolymerization of styrene onto casein initiated by potassium diperiodatonickelate (IV) in alkaline medium

A novel redox system, potassium diperiodatonickelate (Ni(IV))‐casein is used to initiate graft copolymerization of Styrene onto casein under different conditions in aqueous alkaline solution. Graft copolymers with both high grafting efficiency (>98%) and percentage of grafting(>300%) are obtained, which indicated that (Ni(IV))‐casein redox pair is an efficient initiator for this grafting. The effects of reaction parameters, such as monomer‐to‐casein weight ratio, initiator concentration, pH, time, and temperature, are investigated. A tentative initiation mechanism is proposed. The structures and properties of the graft copolymer are characterized by Fourier transform infrared Spectroscopy, X‐ray diffraction diagrams, and Scanning Electron Microscope. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4247–4251, 2006