Noncovalently bonded quinone on self-assembled molecular layers

Aminoalkanethiol surface modifiers were investigated on gold electrodes. It was established, that quinone molecules could be attached to these surface layers in three different forms with well-distinguished redox potentials. Chemical reaction with the amino groups of the modifiers could produce monosubstituted and disubstituted quinones attached covalently to the layers. However, a third form could be detected, as well that seems to be quinone attached non-covalently to the monosubstituted quinone molecules.     

Preparation of silk fibroin and polyallylamine composites

Composite films made of silk fibroin (SF) and polyallylamine (PAA) are prepared that contain various compositional ratios. These materials are analyzed to elucidate the resulting physical properties and to assess their potential toward advanced applications as industrial materials. The composite films are obtained from a SF and PAA binary system by dry casting from aqueous solution. These composite films exhibit excellent processability such as film forming capabilities, and the elongation at break is increased in the wet state. The differential scanning calorimetry (DSC) curves of the composites suggest that a mutual interaction takes place between the SF and PAA. This interaction is believed to occur because the endothermic peak, corresponding to the individual polymer, shifts with increasing SF content. The random coil conformation of the SF is present, regardless of the PAA blending, as confirmed by FTIR and DSC measurements. Additionally, living cells from Antheraea pernyi and Bombyx mori insect tissues are shown to grow effectively on the composite films. Maximum growth levels occur when the cultivation flask is coated with the material in SF/PAA ratios of 75:25 to 25:75. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 1963–1970, 2002; DOI 10.1002/app.10491     

我国电机保护现状与发展趋势

电动机的保护在企业生产中是非常重要的一项内容，其保护方式及过程有一定的规范要求，其发展趋势要遵循可靠、稳定的原则。     

The study on the conductivity of styrene-maleic anhydride copolymer electrolytes based on poly(ethylene glycol)400 and LiClO4

Polyelectrolytes, in this study were synthesized from styrene-maleic anhydride (SMA) copolymer, poly(ethylene glycol)400 (PEG400), and lithium perchlorate (LiClO₄). Fourier transform infrared spectroscopy (FTIR), and magic angle spinning (MAS) solid-state NMR were used to monitor the interaction between Li⁺ ions and polymer. The results of FTIR and MAS solid-state NMR indicate the Li⁺ ions are preferentially coordinated to the ether oxygen of PEG. The T_g of the PEG segments in polyelectrolyte increases with LiClO₄ concentration, as determined by differential scanning calorimetry (DSC), indicating that solubility of the Li⁺ ions in the host polymer increases with the PEG content. Impedance spectroscopy (IS) shows that the bulk conductivity of polyelectrolytes and the conductivity behavior obeys the Vogel-Tamman-Fulcher (VTF) equation.     

Construction of covalently attached enzyme multilayer films based on the photoreaction of diazo-resins and glucose oxidase

A novel and facile approach to construct multilayered glucose oxidase (GOx) films on the surface of quartz or CaF₂ slides as well as gold electrodes for use as biosensing interfaces is described. Diazo-resins (DAR) as polycation and glucose oxidase as polyanion were alternately deposited into a multilayer structure using layer-by-layer self-assembly technique based on electrostatic interaction as driving force. Upon near UV irradiation, the adjacent interfaces of the multilayer reacted to form a crosslinking structure which greatly improved the stability of the enzyme films. These changes was monitored and confirmed by UV-vis and IR spectroscopy. Ellipsometric measurements reveal that the enzymes formed sub-molecule layers, and the thickness of the film shows a linear relationship with the number of assembled layers, demonstrating a spatially well-ordered manner in multilayer structure. The covalently attached enzyme multilayer film has a highly permeable structure, and can be used as biosensing interface. Electrochemical and analytical behavior of the enzyme electrodes was studied by cyclic voltammetry (CV) in the presence or absence of glucose. The sensitivity of the enzyme-modified electrodes was estimated through the analysis of voltammetric signals, which can be fine turned to the desired level by adjusting the number of attached bilayers.     

Fatal Attraction: How Bacterial Adhesins Affect Host Signaling and What We Can Learn from Them

The ability of bacterial species to colonize and infect host organisms is critically dependent upon their capacity to adhere to cellular surfaces of the host. Adherence to cell surfaces is known to be essential for the activation and delivery of certain virulence factors, but can also directly affect host cell signaling to aid bacterial spread and survival. In this review we will discuss the recent advances in the field of bacterial adhesion, how we are beginning to unravel the effects adhesins have on host cell signaling, and how these changes aid the bacteria in terms of their survival and evasion of immune responses. Finally, we will highlight how the exploitation of bacterial adhesins may provide new therapeutic avenues for the treatment of a wide range of bacterial infections.     

焦炭颗粒/热解炭复合材料的制备与压缩性能研究

分别以LJ1、LJ2、YJ、ZJ 4种焦炭颗粒作为增强体,CVD炭作为基体,利用TCVI设备制备出了焦炭颗粒增强热解炭基(焦炭颗粒/热解炭)复合材料。并从其力学性能着手,使用金相显微镜分析其显微结构,采用扫描电镜观察其断口微观形貌,并结合载荷-位移曲线综合分析其断裂方式及机理。结果表明:4种焦炭颗粒/热解炭复合材料中,LJ1和ZJ焦炭颗粒沉积前后密度与质量变化最大,其质量分别增加57.4%和64.3%;焦炭颗粒/热解炭复合材料微观组织结构为各向异性;LJ2焦炭颗粒/热解炭复合材料轴向和径向的压缩强度分别为203.7 MPa和176.3 MPa,在4种焦炭颗粒/热解炭复合材料中强度最高;4种焦炭颗粒/热解炭复合材料压缩断裂方式为脆性断裂,LJ2焦炭颗粒/热解炭复合材料和YJ焦炭颗粒/热解炭复合材料主要是因其内部焦炭颗粒孔洞的应力集中造成断裂,LJ1焦炭颗粒/热解炭复合材料和ZJ焦炭颗粒/热解炭复合材料主要沿其焦炭颗粒的层片断裂。     

Grain growth and crystallinity of ultrafine barium titanate particles prepared by various routes

Variations in tetragonal distortion and the degree of crystallinity of ultrafine BaTiO₃ particles—both industrially applied criteria qualifying their polar characteristics—upon growth during annealing were studied on powders, prepared by the hydrothermal synthesis and by the oxalate route respectively. Regardless of the synthetic route both these properties were found to develop approximately to the same extent with increasing primary particle size. The degree of crystallinity was detectable only above a critical value of c/a=1.007 at an average particle size of around 120 nm. Intragranular porosity in hydrothermal powders and the stoichiometric Ba/Ti-ratio are of minor influence. However, distinct differences in particle growth behavior for both powders were observed. This discrepancy is ascribed to a special morphology of the hydrothermal product, where enhanced particle growth was found to be governed by oriented attachment of individual crystallites and by the motion of solid–solid interfaces.     

Kinetic analysis of NO-sensitized methane oxidation

The role of NO-sensitized oxidation during the product-gas entrainment of a low-NO_x, multi-jet, natural gas burner is investigated. A detailed kinetic mechanism for the NO-sensitized oxidation of CH₄, consisting of 483 reactions and 69 species, is used for the kinetic analysis. An eigenvalue-eigenvector decomposition is performed on normalized sensitivity coefficients to study the important reactions using principal component analysis (PCA), and the loadings corresponding to the largest eigenvalue are used to identify the reaction pathways of NO-sensitized oxidation. The main reaction pathway is most strongly affected by the temperature profile and equivalence ratio. Also, a reduced kinetic scheme of 110 reactions and 47 species is developed by eliminating reactions with small loadings. The temporal evolution of reactions is investigated using functional PCA, in which the functional loadings reflect the importance of reactions as a function of time. A discretization approach is used to perform the functional PCA.     

Assessment of a redox alkaline/iron-chelate absorption process for the removal of dilute hydrogen sulfide in air emissions

The oxidative absorption of hydrogen sulfide (H₂S) into a solution of ferric chelate of trans-1,2- diaminocyclohexanetetraacetate (CDTA) was studied in a counter-current laboratory column randomly packed with 15 mm plastic Ralu rings. The present investigation takes concern about the Kraft pulping situation where dilute H₂S concentrations are omnipresent in large-volume gas effluents. A fractional two-level factorial approach was instigated to determine the significance of six operating variables, namely the solution's alkalinity (pH; 8.5-10.5), the liquid mass flow rate (L;1.73-), the solution's ionic strength (I_C;0.01-), the gas mass flow rate (G;0.19-), the inlet H₂S concentration (C_H2S,0;70-430 ppm) and the initial ferric CDTA concentration (C_Fe,0;100 -). Initially, a Plackett-Burman design matrix of seven duplicated experiments revealed that pH is the leading factor controlling the H₂S conversion rate while the ionic strength and ferric CDTA concentration effects remained negligible within the factorial domain. Surface response analysis based on 11 duplicated factorial experiments plus 10 central composite trials revealed that the H₂S conversion significantly increases with liquid flow rate but decreases with growing H₂S load up. Further examination about the influence of ferric CDTA on H₂S absorption rate was set up over a broader concentration range (C_Fe,0;0- at pH of 9.5 and 10.5. It showed good potential at as H₂S conversion increased by a significant 25% for both pH values in comparison to pure alkaline solutions containing no ferric CDTA.