Mesoporous acid solid as a carrier for metallocene catalyst in ethylene polymerization and a catalyst in catalytic degradation of polyethylene

The possibility of mesoporous acid solid as a carrier for metallocene catalyst in ethylene polymerization and catalyst for polyethylene (PE) catalytic degradation was investigated. Here, HMCM- 41 and AIMCM-41, and mesoporous silicoaluminophosphate molecular sieves (SAPO1 and SAPO2) were synthesized and used as acid solid. Much more gases were produced during catalytic degradation in PE/acid solid mixtures via in situ polymerization than those via physical mixing. The particle size distribution results exhibited that the particle size of SAPO1 in the PE/SAPO1 mixture via in situ polymerization was about 1/14 times of that of the original SAPO1 or SAPO1-supported metallocene catalyst. This work shows a novel technology for chemical recycling of polyolefin.

Partitioning behavior of amino acids in aqueous two-phase systems containing polyethylene glycol and phosphate buffer

The partitioning behavior of four amino acids, cysteine, phenylalanine, methionine, and lysine in 15 aqueous two-phase systems (ATPSs) with different polyethylene glycol (PEG) molecular weights and phosphate buffers has been studied in the present paper. The phase diagrams of the systems are investigated together with the effect of the PEG molecular weight and pH of the phosphate solutions. The composition of these systems and some parameters such as density and refractive index are determined. The influences of salts in ATPSs, side chain structure of the amino acids, pH of ATPSs, and the PEG molecular weight on the distribution ratios of the amino acids have been studied. This work is useful for the purification of amino acids and the separation of some proteins whose main surface exposed amino acid residues are these four amino acids, respectively.

硫堇与寡核苷酸结合序列选择性的光谱研究

用UV-Vis吸收光谱、荧光光谱、圆二色谱以及核磁共振光谱等手段研究了硫堇(TH)与两个不同序列寡核苷酸的作用。TH与寡核苷酸作用后的吸收光谱和荧光光谱产生了明显的减色红移和荧光猝灭效应。分别计算了TH与[oligo d(GC)]2和[oligo d(AT)]2作用的荧光猝灭常数和结合常数,结果表明TH与GC序列的结合能力比与AT序列更强。通过TH与[oligo d(GC)]2作用后双螺旋链构象变化以及TH质子的1HNMR谱峰明显变宽,进一步说明TH与寡核苷酸结合的序列选择性。

Determination of biogenic amines by capillary electrophoresis with pulsed amperometric detection

The biogenic amines, putrescine, cadaverine, spermidine and spermine were separated and quantified by capillary electrophoresis with pulsed amperometric detection. Detection potential of the pulsed amperometric detection was optimized as 0.6 V Optimal separation of the biogenic amines was achieved using a separation buffer of 30 mM citrate at pH 3.5, while keeping the buffer in the detection cell as 20 mM NaOH. Using these conditions, the four biogenic amines were baseline separated. Extrapolated limits of detection for putrescine, cadaverime, spermidine and spermine were 400, 200, 100 and 400 nM for the standard mixture (polyamines dissolved in running buffer), respectively. These are lower than ultraviolet detection and comparable or even lower than laser-induced fluorescence detection results as reported in the literature. The number of theoretical plates was maintained at the 105 level, which is absolutely higher than any reported method. When applying capillary electrophoresis-pulsed amperometric detection to milk analysis, only spermidine was found in amounts varying between 0.1 and 0.5 mg/kg.

纳米CeO_2/阴离子聚氨酯复合材料

采用纳米微粒直接分散法合成了纳米 Ce O2 /阴离子聚氨酯复合材料 ,粘度分析表明 ,随着纳米Ce O2 含量的增加 ,复合材料的粘度降低 ;FT- IR分析表明 ,Ce O2 的吸收峰出现蓝移现象 ;TEM和光散射粒径分析表明 ,复合粒子仍以纳米量级存在 ,平均粒径为 35 nm,且呈单分散状态 ,Ce O2 纳米粒子均匀分散在聚氨酯中。并且对复合粒子形成机理及稳定性进行了初步探讨

Nanometer scale mechanical study on well defined nanostructured chain aggregation of polyethylene

Two kinds of polyethylene chain aggregation with chain axis perpendicular and parallel to the supported substrate were designed and successfully obtained from melt under an electric field and by melt-drawn method

Layer-by-layer assembly of multilayer films composed of streptavidin and biotinylated antibody by real-time biomolecular interaction analysis

Layer-by-layer assembly of multilayer films of streptavidin and biotinylated antibody was completed on the streptavidin coated surface. Real-time biomolecular interaction analysis (BIA) based on surface plasmon resonance technique was used to monitor the multilayer assembly in solution continuously. The results indicate that the uniform multilayer film can be fabricated successfully based on the strong interaction between streptavidin and biotin. The mean surface mass concentration of each adsorption layer is 1. 32 ng/mm(2) for biotinylated antibody, 2. 93 ng/mm(2) for streptavidin, according to the correlation of SPR response with surface concentration.

实时生物分子相互作用分析技术用于链霉亲和素-生物素化抗体的层层组装研究

使用生物分子相互作用分析 ( Biomolecular interaction analysis,BIA)技术实时监测了在链霉亲和素表面层层组装亲和素 -生物素化抗体多层膜的过程 ,结果表明 ,通过链霉亲和素与生物素之间的强亲和作用 ,能够在表面形成均一的多层膜 ,并用实时 BIA技术求得了每层蛋白质的表面浓度 .对于生物素化抗体 ,单层吸附表面浓度为 1 .32 ng/mm2 ;对于链霉亲和素 ,单层吸附表面浓度为 2 .93ng/mm2 .同时对蛋白质在表面的排列状态进行了探讨

Crystal form transition during heating of solvent-induced crystalline syndiotactic polystyrene

The phase transition of two kinds of solvent-induced crystalline syndiotactic polystyrene (sPS). gamma-sPS and delta(c)-sPS, has been studied via WAXD and DSC. gamma-sPS transform to a-sPS at 195-225 degrees C before melt during heating, whereas delta(e)-sPS transform to first gamma-sPS and then a-sPS at 100-200 degrees C and 200-215 degrees C, respectively. The transition of delta(e)-gamma and gamma-a occurs for below melting point of sPS indicates they are all solid-solid transition.

Molecular orientation of copper phthalocyanine in thin films and their gas-sensing properties

Copper phthalocyanine derivative Langmuir-Blodgett (LB) films were prepared by vertical dipping and horizontal lifting methods. Molecular orientation of copper phthalocyanine derivative in thin films was studied by polarized UV-Vis spectra. The relationship between the molecular orientation of copper phthalocyanine in LB films and their gas-sensing properties was investigated.

Electroluminescent properties of the Tris-(acetylsalicylate)-terbium (Tb(AS)(3))

The solubility of [Tris-(acetylsalicylate)-terbium] [Tb(AS)(3)] is improved to a greater extent than [Tris-(salicylate)-terbium] [Tb(Sal)(3)] following introduction of a flexible acetyl group. Th3+ binds with acetylsalicylate in solution at low pH value and the resultant Tb(AS)(3) has good solubility in chloroform. A Green EL device with the structure ITO/PVK/PVB:PBD: Tb(AS)(3)/ PBD/Al has been fabricated based on soluble Tb(AS)(3), in which Tb(AS)(3) was first used as an emissive center doped with PVK and PBD. The hole-transporting layer and the emissive layer were formed by spin coating. The device exhibited a highly pure characteristic green light of Tb3+. (C) 2001 Elsevier Science B.V. All rights reserved.

稀土基汽车尾气催化剂的催化活性研究

利用浸渍法制备了一系列含Ce La稀土助剂改性的Pt Rh三效催化剂 ,采用各种表征手段和高温抗硫水热老化实验 ,考察了Ce La稀土对Al2 O3 载体的热稳定性和催化剂活性的影响 .研究结果表明 ,稀土La2 O3 的添加主要改善了载体Al2 O3 的高温高比表面性能 ;而CeO2 的引入则明显地提高了CO和NO的催化转化活性 ,但对HC的转化几乎无影响 ,也促进了催化剂的抗硫水热老化性能 ,并且显著地拓宽了催化剂的三效窗口 .这主要归因于CeO2的添加 ,它改善了催化剂上CO ,HC和NO间的相互作用以及CeO2 所特有的储氧功能

Synthesis and characterization of (phenolphthalein/4,4 '-thiodiphenol) PES copolymers

Copolymers based on monomers phenolphthalein (PP)/4,4'-thiodiphenol (Bis-T)/4,4'-dichlorodiphenylsulfone (DCDPS) were prepared by a route involving the toluene, N-methyl-2-pyrrolidone and anhydrous potassium carbonate synthesis. The range of optimum reaction temperature was between 185 and 195 degrees C. The copolymers were characterized by C-13 NMR, differential scanning calorimetry (DSC) and torsion braid analysis. It was found that all of the copolymers were random and homogeneous and their glass transition temperatures (T-g) decreased linearly with an increase of Bis-T contents in the copolymers. The thermal stability determined by thermogravimetry analysis in air atmosphere indicated that the copolymer had better resistance to thermo-oxidative degradation. Dynamic mechanical measurement showed that (PP/Bis-T) PES copolymers containing 0-50 mol% of Bis-T components had two secondary relaxations. (C) 1998 Elsevier Science Ltd. All rights reserved.

Pd/C催化剂在处理NO反应中的催化行为

研究了不同活性炭负载的Pd催化剂在NO＋CO反应中和单独处理NO时的催化行为．结果表明，Pd的引入可大大提高催化活性，且活性与Pd含量呈顺变关系．不同的载体对催化剂活性有很大影响．在NO＋CO反应中，由煤质炭为载体制得的催化剂活性很高，在低于550K时NO即可达到100%转化，而在单独NO时，由山桃核炭制得的催化剂有较高的活性，在低于650K时NO可达到100%转化．催化剂活性的差异与活性炭表面性质有关．当反应体系中有还原物质CO存在时，活性炭作为载体，Pd在其上的分散对活性有重要影响；当体系中没有还原物质时，活性炭作为还原剂参与反应，这时活性炭本身的性质变得十分重要.