功能性超薄有序分子沉积膜的制备及其结构研究

1991年G.Decher等首次探讨了阴阳离子与聚电解质交替沉积制备有机超薄膜的方法。我们在完善成膜技术和发展成膜基质的基础上,详细研究了其成膜过程与膜的结构,并定义这种新的自组装超薄有序膜为分子沉积膜——MD膜。MD膜是利用阴阳离子的静电吸附反应特性,通过相反离子体系的交替分子沉积制备的层状有序自组装多层超薄膜。需要指出的是,分子沉积既是有机超薄膜的制备技术,本身又是一种自组装超薄有序膜。MD膜制备工艺简单,热稳定性和长期稳定性好,不受基体形状与面积限制。     

A note of a modular equation of Ramanujan–Selberg continued fraction

The Ramanujan Journal - We show that if $$E/\mathbb {Q}$$ is an elliptic curve with a rational p-torsion for $$p=2$$ or 3, then there is a congruence relation between Ramanujan’s tau function...     

Horseshoe effect and topological entropy of one-dimensional maps

Abstract. In this paper, for any continuous function     

Direct injective modules

Throughout this paperR will denote a ring with idenity element andM a unitary right module overR. AnR-moduleM is said to be direct injective if and only if given direct summandN ofM with injectioni _N:N→M and a monomorphismg:N→M, there exists an endomorphismf ofR-moduleM such thatfg=i _N. In this paper we investigate properties of direct injective modules, and obtain the following results on direct injective modules.

1. We establish the necessary and sufficient condition for a module to be direct injective.
2. We show that the answer on problem of Krull-Schmidt-Matlis is in the affirmative in caseR-moduleM is extending direct injective.
3. We prove that extending direct injectivity of module implies same properties of its direct summands.

     

Three-Dimensional Modeling of the Turbulent Plasma Jet Impinging upon a Flat Plate and with Transverse Particle and Carrier-Gas Injection

Modeling results are presented concerning the turbulent thermal plasma jet impinging normally on a substrate and with transverse injection of feedstock particles and their carrier gas from a single injection tube. The k- two-equation model is employed to model the turbulence, and particle dispersion is studied considering the interaction between the moving particles and turbulent eddies and considering the effect on particle trajectories of the random variation of the turbulent fluctuating velocities in their magnitude and direction. A well-validated three-dimensional (3-D) computer code is used in the modeling. The 3-D effects due to the carrier gas injection on the jet flow field and thus on the particle trajectories and heating histories are shown to be appreciable. The radial location of the injection tube with respect to the plasma jet is shown to be a critical parameter for the study of 3-D effects, besides the carrier-gas/plasma stream mass flux ratio. Particle dispersion considerably widens the distribution of the particle trajectories and heating histories. In addition, although pertinent swirl number is often rather small, swirling may also affect the modeling results.     

A Sterically Hindered Zirconocene Complex (1,2-Ph2C5H3)2ZrCl2:Synthesis, Structure and Properties as Olefin Polymerization Catalyst

SinceKaminskyeIal.discoveredthehighlyactivezirconocenedich1oride/methyl-aluminoxane(MAO)catalyticsystemforolefinpolymerization',intensiveresearchworkhasbeenfocusedondevelopingnewgroup4metal1ocenecatalystsforimprovingcatalystactivitiesandpolymerproperties"'.Inthedevelopmentofnewmetallocenecatalystsystems,liganddesignandmodificationhaveplayedanimportantrole.lthasbeenknownthatevenminormodificationofagivenligandframeworkcouldresultinsignificantchangesincatalystactivitiesandpolymerproperties'.Int…     

Dialane anion: three-center two-electron or two-center one-electron bonded

Dialane anions can be formed via a single three-center two-electron (3c-2e) or two-center one-electron (2c-1e) bond. The 2c-1e bonded anion Al(2)H(6)(-)(D(3)(d)) and the 3c-2e bonded anion Al(2)H(6)(-)(C(s)) have significant thermodynamic stabilities with respect to the neutral Al(2)H(6)(D(2)(h)) and correspond to 0.22 and 0.32 eV of the adiabatic electron affinities, respectively. In particular, the 2c-1e bond plays an essential role in stabilizing the Al(2)H(6)(-)(D(3)(d)) anion.     

Sulfation of hesperetin,naringenin and apigenin by the human cytosolic sulfotransferases: a comprehensive analysis

Abstract

Previous studies have revealed sulfation as a major pathway for the metabolism of hesperetin, naringenin and apigenin. The current study was designed to identify the human cytosolic sulfotransferase (SULT) enzyme(s) capable of sulfating these flavonoid compounds. Of the thirteen human SULTs, six (1A1, 1A2, 1A3, 1B2, 1C4, 1E1) displayed significant sulfating activity toward hesperetin, five (1A1, 1A2, 1A3, 1B2, 1C4) displayed sulfating activity towards naringenin, and four (1A1, 1A2, 1A3, 1C4) showed sulfating activity towards apigenin. Of the four human organ specimens tested, liver and intestine cytosols displayed much higher hesperetin-, naringenin- and apigenin-sulfating activity than lung and kidney cytosols. Moreover, sulfation of hesperetin, naringenin and apigenin was shown to take place in HepG2 human hepatoma cells and Caco-2 human colon adenocarcinoma cells under cultured conditions. Taken together, these results provided a biochemical basis underlying the metabolism of hesperetin, naringenin and apigenin through sulfation in humans.