Self‐assembled complexes of poly(acrylic acid) and poly(styrene)‐block‐poly(4‐vinyl pyridine)

Polymer complexes were prepared from high molecular weight poly(acrylic acid) (PAA) and poly(styrene)‐block‐poly(4‐vinyl pyridine) (PS‐b‐P4VP) in dimethyl formamide (DMF). The hydrogen bonding interactions, phase behavior, and morphology of the complexes were investigated using Fourier transform infrared (FTIR) spectroscopy, differential scanning calorimetry (DSC), dynamic light scattering (DLS), atomic force microscopy (AFM), and transmission electron microscopy (TEM). In this A‐b‐B/C type block copolymer/homopolymer system, P4VP block of the block copolymer has strong intermolecular interaction with PAA which led to the formation of nanostructured micelles at various PAA concentrations. The pure PS‐b‐P4VP block copolymer showed a cylindrical rodlike morphology. Spherical micelles were observed in the complexes and the size of the micelles increased with increasing PAA concentration. The micelles are composed of hydrogen‐bonded PAA/P4VP core and non‐bonded PS corona. Finally, a model was proposed to explain the microphase morphology of complex based on the experimental results obtained. The selective swelling of the PS‐b‐P4VP block copolymer by PAA resulted in the formation of different micelles. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 1192–1202, 2009     

Poly(N-phenyl-2-hydroxytrimethylene amine): Its blends with poly(ϵ-caprolactone) and water-soluble polyethers

A new polymer with pendant hydroxyl groups, namely, poly(N-phenyl-2-hydroxytrime-thylene amine) (PHA), was synthesized by a direct condensation polymerization of aniline and epichlorohydrin in an alkaline medium. The new polymer is amorphous with a glass transition temperature (T_g) of 70°C. Blends of PHA with poly(ϵ-caprolactone) (PCL), as well as with two water-soluble polyethers, poly(ethylene oxide) (PEO) and poly(vinyl methyl ether) (PVME), were prepared by casting from a common solvent. It was found that all the three blends were miscible and showed a single, composition dependent glass transition temperature (T_g). FTIR studies revealed that PHA can form hydrogen bonds with PCL, PEO, and PVME, which are driving forces for the miscibility of the blends. © 1997 John Wiley & Sons, Inc.     

Surface charge of PLA microparticles in regulation of antigen loading,macrophage phagocytosis and activation,and immune effects in vitro

The use of microparticles（MPs） as adjuvants has attracted increasing interest in vaccine delivery systems.Many physiochemical characteristics of MPs including hydrodynamic size,surface properties,and morphology can regulate the immune response.Surface charge is an important characteristic of MPs,but how it affects their adjuvanticity remains unknown.In this study,we prepared uniform-sized polylactide MPs coated with various polymers of different positive charge,and investigated how the surface charge affected antigen loading and macrophage phagocytosis and activation in vitro.A higher surface charge greatly enhanced antigen loading and antigen internalization into macrophages,promoted the expression of MHC 11 and CD80,and increased the secretion level of TNF-a.Taken together,these results indicated that surface charge was an important parameter for improving the adjuvanticity of MPs.     

An improved RNA isolation method for filamentous fungus Blakeslea trispora rich in polysaccharides

Isolation and purification of biologically active RNA from filamentous fungi is difficult because of the complex cell wall and the high level of polysaccharides which bind to or co-precipitate with RNA. Using benzyl chloride and guanidine thiocyanate, RNA was successfully isolated from Blakeslea trispora in which other RNA extraction methods and commercially available kits failed to deliver suitable results. The RNA isolated by this procedure appears to be relatively pure, as it has a ratio of absorbance at 260/280 nm of 1.8–1.9. The integrity of the RNA was further substantiated by RT-PCR and Northern hybridization, respectively. This procedure should be useful for isolating RNA from other filamentous fungi and, therefore, will serve as an important tool for the molecular analysis of these organisms.     

Stochastic and Risk Management Models and Solution Algorithm for Natural Gas Transmission Network Expansion and LNG Terminal Location Planning

Due to the increasing demands for natural gas, it is playing a more important role in the energy system, and its system expansion planning is drawing more attentions. In this paper, we propose expansion planning models which include both natural gas transmission network expansion and LNG (Liquified Natural Gas) terminals location planning. These models take into account the uncertainties of demands and supplies in the future, which make the models stochastic mixed integer programs with discrete subproblems. Also we consider risk control in our models by including probabilistic constraints, such as a limit on CVaR (Conditional Value at Risk). In order to solve large-scale problems, especially with a large number of scenarios, we propose the embedded Benders decomposition algorithm, which applies Benders cuts in both first and second stages, to tackle the discrete subproblems. Numerical results show that our algorithm is efficient for large scale stochastic natural gas transportation system expansion planning problems.     

便携式近红外光谱仪器现状及展望

近红外光谱分析技术具有速度快、操作简单等优点,在农业、制药等行业得到了大量应用,其中一些应用需要将仪器携带到分散的分析现场使用,为满足这一需求,很多体积小、便于移动的便携式近红外光谱仪被研制出来。这些仪器的种类较为繁多,采用了很多不同的基本原理,使用了不同的光路结构。文章综述了国内外便携式近红外光谱仪的技术现状,根据光路结构的不同将仪器分成滤光片型、光栅型、傅里叶变换型、声光可调滤波器型以及使用微机电系统(MEMS)的新型光谱仪等类型,重点介绍各类仪器的原理和主要部分的结构,同时简要介绍不同类型仪器的特点,并列举典型产品。也对测量附件、操作、显示等外围部分的设计作简要介绍,这些附件针对便携应用采取了特殊的设计。通过介绍,为新型便携式近红外光谱仪的研制提供借鉴。最后,对便携式近红外光谱仪器的现状作总结,并对未来国内外技术的发展进行展望。     

基于NLMS自适应滤波的近红外光谱去噪处理方法研究

为了去除直接采集的近红外(NIR)光谱中含有的噪声,将归一化最小均方(NLMS)自适应滤波方法引入到NIR光谱去噪领域中。以51份土壤样品的NIR光谱为研究对象,探讨NLMS自适应滤波方法在NIR光谱预处理中的应用,并将处理后的结果与土壤中有机质的含量相关联,建立模型。结果表明,通过NLMS自适应滤波去噪后的光谱,预测集的相关系数r由处理前的0.8284提高至0.9654,预测均方根误差(RMSEP)由处理前的0.3385降至0.1606。由此可见,NLMS自适应滤波对NIR光谱的去噪有显著效果,可以有效地提高光谱的分析精度和模型的稳健性,为NIR光谱的预处理提供了一种新方法。     

Poly(hydroxyether of phenolphthalein) and its blends with poly(ethylene oxide)

Poly(hydroxyether of phenolphthalein) (PPH) was synthesized through the polycondensation of phenolphthalein with epichlorohydrin. It was characterized by Fourier transform infrared (FTIR) spectroscopy, NMR spectroscopy, and differential scanning calorimetry (DSC). The miscibility of the blends of PPH with poly(ethylene oxide) (PEO) was established on the basis of the thermal analysis results. DSC showed that the PPH/PEO blends prepared via casting from N,N‐dimethylformamide possessed single, composition‐dependent glass‐transition temperatures. Therefore, the blends were miscible in the amorphous state for all compositions. FTIR studies indicated that there were competitive hydrogen‐bonding interactions with the addition of PEO to the system, which were involved with OH…O?C〈, ? OH…? OH, and ? OH vs ether oxygen atoms of PEO hydrogen bonding, that is both intramolecular and intermolecular, between PPH and PEO). Some of the hydroxyl stretching vibration bands significantly shifted to higher frequencies, whereas others shifted to lower frequencies, and this suggested the formation of hydrogen bonds between the pendant hydroxyls of PPH and ether oxygen atoms of PEO, which were stronger than the intramolecular hydrogen bonding between hydroxyls and carbonyls of PPH. The FTIR spectra in the range of carbonyl stretching vibrations showed that the hydroxyl‐associated carbonyl groups were partially set free because of the presence of the competitive hydrogen‐bonding interactions. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 466–475, 2003     

Integrated Suzuki Cross-Coupling/Reduction Cascade Reaction of meta-/para-Chloroacetophenones and Arylboronic Acids under Batch and Continuous Flow Conditions

Overcoming the incompatibility of a pair of conflicting catalysts via a flow methodology has great significance in the practical applications for multistep organic transformations. In this study, a multiple continuous-flow system is developed, which can boost the reactivity and selectivity in a sequential enantioselective cascade reaction. During this process, a periodic mesoporous organosilica-supported Pd/carbene species as a Suzuki cross-coupling catalyst is packed in the first column reactor, whereas another periodic mesoporous organosilica-supported Ru/diamine species as an asymmetric transfer hydrogenation catalyst is packed in the second column reactor. As we envisioned, the initially Pd-catalyzed cross-coupling reaction of meta-/para-chloroacetophenones and aryl boronic acids followed by the subsequentially Ru-catalyzed reduction provides chiral biarylols with enhanced yields and enantioselectivities. Furthermore, the advantages of the easy handling and the simple procedure make this system an attractive application in a scale-up preparation of optically pure organic molecules under environmentally-friendly conditions.