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排序方式: 共有300条查询结果,搜索用时 15 毫秒
1.
Optimization technologies and environmental applications 总被引:1,自引:0,他引:1
2.
G. Carelli N. Ioli A. Messina A. Moretti S. Schepis F. Strumia 《International Journal of Infrared and Millimeter Waves》1998,19(9):1191-1199
We measured the dependence of the reflectivity of InSb crystals upon temperature in the submillimeter region using monochromatic radiation from an optically pumped far infrared (FIR) laser. The measures allowed us to determine the value of the electron effective mass at low temperatures with radiations of different frequencies. Our measurements extend the results obtained recently on pure crystals with magneto-optical methods to the low temperatures region where only old measures were available. 相似文献
3.
Ovshinsky SR Young RT Allred DD DeMaggio G Van der Leeden GA 《Physical review letters》1987,58(24):2579-2581
4.
Filippo Samperi Concetto Puglisi Rosario Messina Antonino Recca Andrea Scamporrino 《Polymer Degradation and Stability》2007,92(7):1304-1315
Pyrolysis products with mass of up to 850 Da were detected by direct pyrolysis mass spectrometric (DPMS) analysis of a series of copoly(arylene ether sulfone)s (PES-PPO) synthesized by nucleophilic condensation of either 4,4′-dichlorodiphenylsulfone (CDPS) or 4,4′-bis-(4-chlorophenyl sulfonyl) biphenyl (long chain dichloride, LCDC) with different molar ratios of hydroquinone (HQ) or dihydroxydiphenylsulfone (HDPS). Pyrolysis products retaining the repeating units of the initial copolymers were formed at temperatures ranging from 420 °C to 470 °C (near the initial decomposition temperature). At temperatures higher than 450 °C were observed products containing biphenyl units, formed by the elimination process of SO2 from diphenyl sulfone bridges. Products having biphenyl and dibenzofuran moieties were detected in the mass spectra recorded at temperatures above 550 °C. These units were formed by loss of hydrogen atom from diphenyl ether bridges. Although the EI (18 eV) mass spectra of the pyrolysis products of the samples investigated were very similar, it was found that the relative intensity of some ions reflects the molar composition of the copolymers analysed. Cyclic and linear oligomers with very low molecular mass, present in the crude copolymers, were also detected by DPMS. Thermogravimetric analysis also showed their excellent thermal stability below 400 °C. It indicates that the copolymers yield a char residue of 40-45% at 800 °C, which increases with the PPO mole fraction in the samples. 相似文献
5.
Paula?Messina Marcela?A.?Morini Pablo?C.?SchulzEmail author 《Colloid and polymer science》2003,281(7):695-698
The hydration of micellised sodium dehydrocholate molecules was determined by viscosity measurements. It was found that there are 39 water molecules for each micellised surfactant molecule. About ten water molecules may be attributed to the hydration of the sodium carboxylate group. By assignation of two water molecules to each of the three carbonyl groups, the total hydration of a micellised sodium dehydrocholate molecule was estimated as about 16 water molecules. The remaining 23 water molecules per micellised sodium dehydrocholate molecule may be attributed to water trapped in the structure of micelles. 相似文献
6.
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8.
Paula Messina Marcela A. Morini Pablo C. Schulz Gerardo Ferrat 《Colloid and polymer science》2002,280(4):328-335
We used a battery of different methods to study the association in aqueous sodium dehydrocholate (NaDHC) solutions. This
salt associates by a stepwise mechanism. Below (9.6 ± 4.2) × 10−4 mol dm−3 there is a molecular solution with some strongly insoluble dehydrocholic acid produced by hydrolysis. Between (9.6 ± 4.2) × 10−4 and (5.2 ± 2.2) × 10−3 mol dm−3, an aggregate similar to acid soap (NaDHC.HDHC) appears and its amount and the aggregate's size increase with concentration.
At =(2.20 ± 0.85) × 10−2 mol dm−3 the aggregates formed have properties usually associated with true micelles, such as solubilisation of water-insoluble dyes.
These aggregates increase in size with concentration and change their shape at 8 × 10−2 mol dm−3, giving nonsymmetrical aggregates. The changes in the solution physicochemical properties at these concentrations may be
misinterpreted and this explains the different values of the critical micelle concentration reported in the literature for
substances with similar structure, such as bile salts.
Received: 14 May 2001 Accepted: 10 August 2001 相似文献
9.
A critical comparison of approximation methods and models for equilibrium properties of low-barrier hydrogen bonds 总被引:1,自引:0,他引:1
MacDonald DA Eppard GE Halkides CJ Messina M 《Journal of chemical information and computer sciences》2002,42(6):1390-1397
Recent experimental evidence has led to the conclusion that short, strong hydrogen bonds can stabilize transition states of enzyme catalyzed biochemical reactions. Evidence for such hydrogen bonds is the low value of the isotopic fractionation factor, phi, which is defined as the equilibrium constant for the generic reaction, R-H + DOH <--> R-D + HOH, where H is the hydrogen atom participating in the low-barrier hydrogen bond in a molecule R-H. In this work we assess two approximation methods for computing the isotopic fractionation factors for single and multidimensional systems containing a low-barrier hydrogen bond. These methods are WKB and an approach that corrects the classical partition function via a quantum correction factor. We find that the latter approach is universally accurate and applicable in both single and multidimensional systems containing a low-barrier hydrogen bond. We also assess two different models for the coupling of a molecule's low-barrier hydrogen bond to other degrees of freedom, both internal and external to the molecule, and show that each leads to a lowering of the fractionation factor. 相似文献
10.
Francesco Frusteri Lorenzo Spadaro Claudia Espro Adolfo Parmaliana Francesco Arena 《天然气化学杂志》2002,(Z2)
The liquid-phase partial oxidation of propane in the presence of the Fen+/H2O2 Fenton system at 70℃ and 1.4 atm on silica supported Nafion catalysts has been investigated. The reaction proceeds via a radical reaction path the efficiency of which is improved by silica-supported Nafion catalysts. Because of the direct relationship between reaction rate and concentration of sulphonic acid sites of Nafion catalysts, it is inferred that the active phase enahnces the kinetics of propane conversion by promoting the rate of active radicals generation. 相似文献