阴离子型微乳液对火焰原子吸收法测铅增敏作用的研究与应用

研究了在空气－乙炔火焰中，阴离子型表面活性剂十二烷基硫酸钠（ＳＤＳ）组成的微乳液对铅原子化行为的影响。结果表明：在ＳＤＳ组成的微乳液存在下，铅的灵敏度提高了近６０％，比ＳＤＳ胶束存在下灵敏度也提高了２０％。方法用于黄铅和工业废水中铅的测定，结果令人满意。     

A coloured ferroelectric side chain polymer

Abstract

Coloured ferroelectric liquid-crystalline side chain copolymers containing 5 per cent and 15 per cent of an azo dye were synthesized and characterized by DSC, GPC and optical microscopy. Order parameters, S, of the azo compound exceeding 0·8 were measured in the frozen smectic phase for the 5 per cent copolymer. The copolymers exhibit fast electrooptic switching in the range of a few hundred microseconds to milliseconds in the S_c* phase. Both linear (i.e. electroclinic-like) and ferroelectric switching have been observed. Tilt angles of ～19° and spontaneous polarization of ～300nC cm^?2 have been recorded in the S_c* phase.     

异质Stackelberg寡头竞争下创新产品技术许可策略研究

基于异质产品Stackelberg寡头竞争模型,建立了拥有新产品创新技术在位厂商与潜在竞争对手间的技术许可博弈模型.模型中假设潜在竞争对手可以接受许可,也可通过自我研发创新技术进入市场参与竞争.根据潜在竞争对手研发成本的高低,研究了创新厂商的最优两部制收费策略.研究结果表明:潜在竞争者总会接受创新技术许可,最优许可策略依赖于研发成本、市场参数以及产品的替代系数.     

养护条件对UHPC强度和毛细吸水性的影响

为优化超高性能混凝土(UHPC)预制构件养护工艺,研究了不同养护条件对UHPC强度和毛细吸水性的影响,并采用孔结构测试、热重分析和扫描电镜观察,对其机理进行了分析.结果表明:热养护显著提高了UHPC的7 d强度,这与加速火山灰反应有关,但高温和干热养护对其后期强度增大不利,甚至出现约3％的强度倒缩;不论何种养护,UHP...     

A conformational study of phospha(III)- and phospha(V)-guanidine compounds

Spectroscopic, crystallographic, and computational studies of the substituent distribution about the "NCN" unit in a series of phospha(III)- and phospha(V)-guanidines, R(2)PC{NR'}{NHR'} and R(2)P(E)C{NR'}{NHR'} (R = Ph, Cy; R' = (i)Pr, Cy; E = S, Se), are reported. In the phosphorus(III) systems, the P-diphenyl substituted compounds are observed as only one isomer, shown by NMR spectroscopy to be the E(syn)-(alpha) configuration. In contrast, the corresponding P-dicyclohexyl derivatives exist as a mixture of E(syn)-(alpha) and Z(anti) in solution. Spectroscopic techniques are unable to determine whether the latter isomer exists as the alpha- or beta-conformer relative to rotation about the P-C(amidine)() bond; however, DFT calculations indicate a low-energy structure for the N,N'-dimethyl model complex in the beta-conformation. In their oxidized sulfo and seleno forms, the P-diphenyl compounds are present as an interconverting equilibrium mixture of the E(syn)-(beta) and Z(syn)-(beta) isomers in solution ( approximately 3:2 ratio), whereas for the P-dicyclohexyl analogues, the latter configuration (in which the nitrogen substituents are in a more sterically unfavorably cisoid arrangement about the imine double bond) is the dominant form. Intramolecular E...HN (E = S, Se) interactions are observed in solution for the Z(syn)-(beta) configuration of both P-substituted species, characterized by J(SeH) coupling in the NMR spectrum for the P(V)-seleno compounds and a bathochromic shift of the NH absorption in the infrared spectrum. An X-ray crystallographic analysis of representative Ph(2)P(E)- and Cy(2)P(E)-substituted species shows exclusively the E(syn)-(beta) configuration for the P-diphenyl substituted compounds and the Z(syn)-(beta) form for the P-dicyclohexyl derivatives, independent of the chalcogen and the nitrogen substituents. Results from a DFT analysis of model compounds fail to identify a compelling electronic argument for the observed preferences in substituent orientation, suggesting that steric factors play an important role in determining the subtle energetic differences at work in these systems.     

A characterization of the Raman modes in a J-aggregate-forming dye: a comparison between theory and experiment

J-Aggregates are a class of organic molecules that possess several interesting characteristics that make them attractive for a range of organic-based optoelectronic devices. We present experimental and computer-simulation studies of the Raman-active vibrational modes in the J-aggregate-forming dye 5,6-dichloro-2-[[5,6-dichloro-1-ethyl-3-(4-sulfobutyl)benzimidazol-2-ylidene]propenyl]-1-ethyl-3-(4-sulfobutyl)benzimidazolium hydroxide, sodium salt, inner salt. The molecular monomer and dimer are analyzed computationally and the Raman mode energies extracted. There is a good agreement between the energies of the theoretical and experimental Raman modes. Experimentally, an enhancement is seen in the intensity of two low frequency modes upon aggregation of the dye. This is attributed to aggregation-enhanced Raman scattering. An enhancement is also observed in certain modes of the calculated spectra upon changing from a monomer to dimeric arrangement. A link is suggested between the Raman-active vibrational modes of the molecule, and a time-dependent electronic coupling present over several molecules.     

Molecular mechanisms of aqueous boundary lubrication by mucinous glycoproteins

Mucins have long been recognized as instrumental to biolubrication but the molecular details of their lubrication mechanisms have only been explored relatively recently. The glycoprotein PRG4, also known as lubricin, shares many features with mucins and appears to lubricate through similar mechanisms. A number of studies have contributed to a more in-depth understanding of mucin adsorption and layer formation on surfaces and the mechanisms by which these layers lubricate. Although mucinous glycoproteins differ in their aggregation properties, their adsorption behaviors on surfaces, and in their ability to reduce friction, they share important similarities favorable for lubrication. They are highly hydrated, they adsorb strongly to a broad range of surfaces, and the layers they form are both sterically and electrostatically repulsive, all attributes thought to contribute to boundary lubrication. They also hydrophilize hydrophobic surfaces, promoting the formation of aqueous fluid films that can lower friction at already relatively low sliding speeds. In this paper we briefly review current knowledge of mucin adsorption and lubrication, with a focus on recent advances.     

The effect of P-cyclohexyl groups on the coordination chemistry of phosphaguanidinates

The anion of P-dicyclohexylphosphaguanidine, Cy2PC{NiPr}{NHiPr}, forms a P,N-chelate at lithium and cobalt(II); bridging through the Nimine atom forms cyclic hexamers in the former complex.