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51.
Adopting a stationary phase convention circumvents problematic definition of the boundary between the stationary and the mobile phase in the liquid chromatography, resulting in thermodynamically consistent and reproducible chromatographic data. Three stationary phase definition conventions provide different retention data, but equal selectivity: (i) the complete solid phase moiety; (ii) the solid porous part carrying the active interaction centers; (iii) the volume of the inner column pores. The selective uptake of water from the bulk aqueous‐organic mobile phase significantly affects the volume and the properties of polar stationary phases. Some polar stationary phases provide dual‐mode retention mechanism in aqueous‐organic mobile phases, reversed‐phase in the water‐rich range, and normal‐phase at high concentrations of the organic solvent in water. The linear solvation energy relationship model characterizes the structural contributions of the non‐selective and selective polar interactions both in the water‐rich and organic solvent‐rich mobile phases. The inner‐pore convention provides a single hold‐up volume value for the retention prediction on the dual‐mode columns over the full mobile phase range. Using the dual‐mode monolithic polymethacrylate zwitterionic micro‐columns alternatively in each mode in the first dimension of two‐dimensional liquid chromatography, in combination with a short reversed‐phase column in the second dimension, provides enhanced sample information. 相似文献
52.
Wen‐Jing Zhao Xu‐Yan Chen Yu‐Qian Liu Ping Li Hui‐Jun Li 《Journal of separation science》2020,43(9-10):1755-1772
Alkaloids are a widespread group of basic compounds in herbal medicines and have attracted great interest due to various pharmaceutical activities and desirable druggability. Their distinctive structures make chromatographic separation fairly difficult. Peak tailing, poor resolution, and inferior column‐to‐column reproducibility are common obstacles to overcome. In order to provide a valuable reference, the methodologies and/or strategies on liquid chromatographic separation of alkaloids in herbal medicines proposed from 2012 to 2019 are thoroughly summarized. 相似文献
53.
R. Anbarasan V. Sangeeth M. Saravanan R. Rajkumar M. Anandhaalaguraja V. Dhanalakshmi 《Journal of Macromolecular Science: Physics》2013,52(4):704-719
Effects of substituents and dopants on the structure–property relationships of poly(aniline) (PANI)-type homopolymers are analyzed. The gravimetric method was used for the estimation of rate of polymerization (Rp). FTIR spectroscopy was used for the calculation of relative intensities (RI) of benzenoid (RI[B/CH]), quinonoid (RI[Q/CH]), and their internal conversion (RI[B/Q]). Thermogravimetric analysis (TGA) characterized the thermal stability of PANIs. A standard four probe method was employed for the conductivity measurements. The results are analyzed and critically compared. 相似文献
54.
Yasemin Yuksel Durmaz Marco Sangermano Yusuf Yagci 《Journal of polymer science. Part A, Polymer chemistry》2010,48(13):2862-2868
A novel method for surface modification of UV‐cured epoxy network was described. Photoinitiated cationic copolymerization of a bisepoxide, namely 3,4‐epoxy cyclohexylmethyl 3,4‐epoxycyclohexanecarboxylate (EEC) with epibromohydrine (EBH) by using a cationic photoinitiator, [4‐(2‐methylpropyl)phenyl]4‐methylphenyl‐iodonium hexafluorophosphate, in propylene carbonate solution was studied. The real‐time Fourier transform infrared spectroscopic, gel content determination and thermal characterization studies revealed that both EEC and EBH monomers take part in the polymerization and epoxy network possessing bromomethyl functional groups was obtained. The bromine functions of the cured product formed on the glass surface were converted to azide functionalities with sodium azide. Independently prepared alkyne functional poly(ethylene glycol) (PEG) was subsequently anchored to azide‐modified epoxy surface by a “click” reaction. Surface modification of the network through incorporation of hydrophilic PEG chain was evidenced by contact angle measurements. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2862–2868, 2010 相似文献
55.
Vicari L 《The European physical journal. E, Soft matter》2002,9(4):335-340
We present a new pump probe laser beams configuration for the nonlinear optical characterization of microemulsions. We detect
the variation of the on-axis optical intensity of the probe beam as generated by the concentration profile induced in an optically
thin film of microemulsion by the pump beam. A mathematical model has been introduced to describe the phenomenon. The technique
allows the determination of both Kerr-like optical nonlinearity and time constants and, therefore, it gives information both
on cluster dimension and their shape. We discuss its application to WAD (water/AOT/decane, where AOT denotes sodium-bis-di-ethyl-sulfosuccinate)
with the application of a strong electric field of optical source. Comparison between theoretical predictions and experimental
results confirms the presence of giant optical nonlinearity in the absence of turbidity divergence. Chainlike shape of clusters,
of the kind already reported with the application of strong electric field, could justify this result.
Received 26 October 2002
RID="a"
ID="a"e-mail: vicari@na.infn.it 相似文献
56.
Koga T 《The European physical journal. E, Soft matter》2005,17(3):381-388
The formation of intramolecular micelles in copolymers with periodic sequence, where hydrophobic units (stickers) are periodically placed along the chain, is studied by using multicanonical Monte Carlo computer simulations for an off-lattice bead-rod model in three dimensions. With decreasing the temperature, a transition from random-coil conformations to micelles occurs and flower-type micelles are formed via the transition. The number of stickers forming a micelle core is limited by the excluded-volume effect of loop chains around micelle cores. By this effect, two intramolecular micelles are formed for long polymer chains with 60 bonds via the coil-to-micelle transition. By further decreasing the temperature, we find that another transition, i.e., a micelle-to-micelle transition, takes place. At this transition point, the two intramolecular micelles merge into one micelle. Furthermore, we extend the multicanonical MC method to study elastic properties of single polymer chains with strong attractive interactions under external force fields, and study how the intramolecular micellization affects the elastic property of single polymer chains. 相似文献
57.
We investigate the structural behavior of a poly(styrene)-block-poly(acrylic acid) diblock copolymer which forms hexagonally-packed PS cylinders (C-phase) in the melt state. The water dispersion of this structure provides hairy cylinders which comprise a PAA swollen cylindrical brush with a height h tunable via its degree of ionization and the ionic strength in the solution, and a water-free, PS cylindrical core of constant radius RC. Such system constitutes an out-of-equilibrium frustrated model system: the selective swelling of the PAA brush results in a frustration of the interface curvature, which the ratio h/RC allows to quantify. Upon heating at a temperature higher than the glass transition temperature of the PS core, the glassiness of the core is relieved and the mechanical constraints arising from the selective swelling of the structure can be relaxed: the cylinders undergo a cylinder-to-sphere transition upon annealing at high temperature, when above a frustration threshold h/RC 1.8. Thanks to a careful mapping of the transition diagram, an undulating cylindrical morphology (UC) is identified between unchanged cylinders ( h/RC
1.8) and spheres ( h/RC 2.0), which appears to result from a Rayleigh-like pearling instability of the copolymer cylinders. 相似文献
58.
Oelschlaeger C Buhler E Waton G Candau SJ 《The European physical journal. E, Soft matter》2003,11(1):7-20
The mixed micellization between the cationic gemini surfactant [ C12H25( CH3)2N+( C2H4) N+( CH3)2 C12H25•2Br-] and the cationic cetyltrimethylammonium bromide (CTAB) in 150 mM KBr solutions has been investigated. The variation of the
cmc of the mixtures, measured by surface tension experiments, with composition revealed synergism in micelle formation. T-Jump
and light scattering experiments performed in the vicinity of the crossover volume fraction showed the existence of two micellar
populations, possibly linear and toroidal micelles. Rheological and dynamic light scattering experiments allowed to fully
characterize the linear viscoelasticity of the mixtures. These measurements revealed synergistic gains in viscoelastic properties
with a maximum of the stress-relaxation time around the equimolar composition. These effects are ascribed to a progressive
intermicellar crosslinking resulting from a continuous increase of the end-cap energy with the 12-2-12 content in the mixture.
Received: 18 November 2002 / Accepted: 8 April 2003 / Published online: 27 May 2003
RID="a"
ID="a"e-mail: candau@fresnel.u-strasbg.fr 相似文献
59.
A. Dobrak B. Verrecht H. Van den Dungen A. Buekenhoudt I.F.J. Vankelecom B. Van der Bruggen 《Journal of membrane science》2010
This paper describes solvent flux and rejection behavior of different hydrophilic TiO2 membranes and a hydrophobic ZrO2 membrane. Solvents and solutes used range from polar to non-polar. Additionally, the temperature effect on permeability and rejection of solutes through these membranes was examined. 相似文献
60.
Guido Barone Giuseppina Castronuouvo Vittorio Elia Maria Teresa Tosto 《Journal of solution chemistry》1986,15(2):199-210
The excess enthalpies of twelve ternary aqueous solutions of alcohols or monosaccharides containing thiourea have been determined by flow microcalorimetry at 25°C. The coefficients of the virial expansion of the excess enthalpies are compared with those reported in the literature for the same ternary solutions containing urea in place of thiourea. The cross-interaction coefficients are positive for the thiourea-alcohol systems and depend on the length and branching of the alkyl chain of the alcohols. On the other hand, they are negative for the thiourea-monosaccharide systems. Thus, thiourea, as urea, can be used as a probe to reveal differences in the behavior of families of solutes characterized by the same functional groups. The results can be interpreted in terms of the relative stabilities of hydration cospheres of hydrophobic or hydrophilic solutes toward a chaotropic agent such as thiourea.Presented at the sixth Italian meeting on Calorimetry and Thermal Analysis (AICAT) held in Naples, December 4–7, 1984. 相似文献