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1.
Jilly James Chidambaram Ramalechume Asit Baran Mandal 《Journal of Polymer Science.Polymer Physics》2007,45(17):2410-2420
The shape, size, aggregation, hydration, and correlation times of water insoluble PEO‐PPO‐PEO triblock copolymer micelles with sodium dodecylsulfate (SDS) micelles were investigated using transport studies and dynamic light scattering technique. From the conductance of micellar solutions of the polymer in 25 mM SDS and 5 mM NaCl, the hydration of polymer micelles were determined using the principle of obstruction of electrolyte migration by the polymer. The asymmetry of the micellar particles of polymer and polymer‐SDS mixed micellar systems in 5 mM NaCl and their average axial ratios were calculated using intrinsic viscosity and hydration data obeying Simha–Einstein equation. Hydration number and micellar sizes were variable with temperature. The shape of the polymer micelles has been ellipsoidal rather than spherical. The micellar volume, hydrodynamic radius, radius of gyration, diffusional coefficients as well as translational, rotational and effective correlation times have been calculated from the absolute values of the axes. The partial molal volume of polymer micelles has also been determined and its comparison with the molar volume of pure polymer suggested a volume contraction due to immobilization of the water phase by the hydrophilic head groups of the polymer. The thermodynamic activation parameters for viscous flow favor a more ordered water structure around polymer micelles at higher temperatures. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 2410–2420, 2007 相似文献
2.
Aryl substituted α-carbonyl bromo-alkynes undergo facile cyclizations to the corresponding substituted 4-methylene-tetrahydrofurans using indium(I) iodide in acetonitrile under sonication in high yields. The reaction is predicted to proceed via a radical process initiated by InI and a plausible radical pathway is suggested. 相似文献
3.
Using the multipoles method, we formulate the problems of radiation (both heave and sway) of water waves by a submerged sphere
in deep as well as in uniform finite depth water with an ice-cover, with the ice-cover being modelled as an elastic plate
of very small thickness. In each case this leads to an infinite system of linear equations which are solved numerically by
standard techniques. The added-mass and damping coefficients for a heaving and swaying sphere are obtained and depicted graphically
against the wave number for various values of the radius of the submerged sphere and flexural rigidity of the ice-cover to
show the effect of the presence of ice-cover on these quantities. When the flexural rigidity is taken to be zero, the numerical
results for the added-mass and damping coefficient for water with a free surface are recovered. 相似文献
4.
Rao DP Sivakumar SV Mandal S Kota S Ramaprasad BS 《Journal of chromatography. A》2005,1069(1):141-151
The separation of propylene-propane mixture is an energy intensive operation commercially practiced using cryogenic distillation. The separation by pressure swing adsorption has been studied as an alternative. A fixed-bed pressure swing adsorption yields the heavy component as a pure product. The product recovery and the productivity are not high. In a moving-bed process, because of the counter-current solid-gas contact, the separation achieved is similar to that of the fractionation by distillation. Although the moving-bed operation offers the upper limit for the performance of a cyclic adsorptive process, due to mechanical complexities in the handling of solids the 'simulated' moving-bed is preferred. By moving the inlet and outlet ports of streams located along the length of the bed, a moving-bed process can be realized in a fixed bed. We describe here a 'moving-port' system which permits injection or withdrawal of the fluid along the axial direction in a fixed bed. A fixed bed embedded with the moving-port systems emulates a simulated moving-bed adsorber. The proposed adsorber can fractionate a binary gas mixture into two product streams with high purities. It is similar to the Sorbex process of UOP but does not have the eluent as an additional separating agent. A parametric study indicates that high purity products and a higher productivity by an order of magnitude can be achieved with simulated moving-beds compared to the fixed beds. 相似文献
5.
The phase diagram for the ternary system deca glycerol dioleate(DGD)/heptane/water was established at 25 °C. In this phase diagram it was seen that the reverse micellar solution phase extends in its area until the water content reaches 35–45 wt%, at which a liquid crystalline phase begins to appear. On the basis of the experimental results of specific conductivity, viscosity, etc. for the samples containing a definite amount of DGD (0,1 M), and varying relative amounts of heptane and water, the mechanism of the transition of reverse micellar structures to liquid crystalline phase is discussed. 相似文献
6.
Mandal PK Kaluarachchi KK Ogrin D Bott SG McMurray JS 《The Journal of organic chemistry》2005,70(24):10128-10131
[reaction: see text] Azabicyclo[X.Y.0]alkane amino acids are rigid dipeptide mimetics that are useful tools for structure-activity studies in peptide-based drug discovery. Herein, we report an efficient synthesis of three diastereomers of 9-tert-butoxycarbonyl-2-oxo-3-(N-tert-butoxycarbonylamino)-1-azabicyclo[4.3.0]nonane (3S,6S,9S, 3S,6R,9R, and 3S,6R,9S). Methyl N-Boc-pyroglutamate is cleaved with vinylmagnesium bromide to produce an acyclic gamma-vinyl ketone. Michael addition of N-diphenylmethyleneglycine tert-butyl ester produces the N-Boc-delta-oxo-alpha,omega-diaminoazelate intermediate, which, on hydrogenloysis, gives the fused ring system. Acidolytic deprotection followed by Fmoc-protection provided building blocks suitable for solid-phase synthesis. 相似文献
7.
Amphiphilic polymers consisting of a statistical distribution of octadecyl methacrylate (ODMA) and acrylic acid in respective molar ratios of 83-22 and 17-78 mol% and in a molecular-weight range of 2.35-4.70᎒4 gmol-1 have been synthesized. The series of polymers consisting of various mole fractions of ODMA and acrylic acid are expected to exhibit unique characteristics resembling ionomer to hydrophobically modified polyelectrolytes. The changes in the I3/I1 emission intensity ratios of pyrene, occurring in the presence of tetrahydrofuran (THF) solutions of the polymers have been taken as the main basis for inferring solution structures. The polymers are found to form random-coil to collapsed-coil/aggregated structures in THF solvent depending on the copolymer compositions. The polymer consisting of 83 mol% ODMA and 17 mol% acrylic acid behaves as an ionomer, capable of forming collapsed-coil structures at concentrations of 0.02 gml-1 and above as shown by a very high I3/I1 of 1.20 (I3/I1 of pyrene in THF is 0.85). In contrast, the poly(octadecyl methacrylate) homopolymer and the sets of copolymers consisting of a very high proportion of acrylic acid to an extent of 73 mol% and above contribute to almost negligible or very small changes in I3/I1 similar to the homopolymer, poly(octadecyl methacrylate), suggesting the formation of random-coil structures. 相似文献
8.
Indrajit Kar B. M. Mandal S. R. Palit 《Journal of polymer science. Part A, Polymer chemistry》1969,7(10):2829-2836
Chain transfer constants of some fluoroalcohols [HCF2(CF2)n?1CH2OH, n = 2, 4, 6] in the catalyzed polymerization of vinyl acetate, styrene, acrylonitrile, and methyl methacrylate at 60°C have been evaluated by a method based on degree of polymerization. Since fluoroalcohols are normally nonsolvents for polymers, a homogeneous reaction phase is maintained by carrying out the polymerization in benzene (except in case of acrylonitrile, where no solvent was used). The transfer constants vary, depending on the reactivity as well as the polarity of the radicals, in the following order: vinyl acetate > styrene > methyl methacrylate > acrylonitrile. Of the three fluoroalcohols studied, the transfer constants increase with the increasing value of n. The results have been interpreted in terms of polar structure contribution in the transition state of the transfer reactions. 相似文献
9.
S. Bhattacharya A.N. Mandal S.R. Ray Chaudhuri A. Chatterjee 《Tetrahedron letters》1984,25(28):3007-3010
An efficient ring contraction of stereoisomeric 1,2-benzo-4-bromo-3-hydroxycyclohept-1-ene and their derivatives (1a-e) to (2a-c) is reported, and a probable mechanism for this ring contraction has been suggested. 相似文献
10.
The hydroboration of cis-2-butene and cis-3-hexene with pure diisopinocampheylborane (IPC2BH) and monoisopinocampheylborane (IPCBH2), both prepared from (+)-α-pinene, were studied. In contrast to IPC2BH, which yielded R-(?)-2-butanol and R-(?)-3-hexanol in 98.4 and 94.5% optical purities, IPCBH2 yielded S-(+)-2-butanol and S-(+)-3-hexanol in 23.6 and 19.7% optical purifies respectively. PMR examination of the methanolyzed products were utilized to establish the species present in the freshly prepared and aged adduct from (+)-α-pinene and BH3 · THF. The results confirm the interpretation previously advanced for the major differences realized in asymmetric hydroboration with the fresh and aged adducts. 相似文献