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1.
K. Y. Sandhya C. K. S. Pillai K. Sree Kumar 《Journal of Polymer Science.Polymer Physics》2004,42(7):1289-1298
New hydrogen‐bonded liquid‐crystalline poly(ester amide)s (PEA)s were obtained from 1,4‐terephthaloyl[bis‐(3‐nitro‐N‐anthranilic acid)] (5) or 1,4‐terephthaloyl[bis‐(N‐anthranilic acid)] (6), with or without nitro groups, respectively, through the separate condensation of each with hydroquinone or dihydroxynaphthalene. The dicarboxylic monomers were synthesized from 2‐aminobenzoic acid. The phase behavior of the monomers and polymers were studied with differential scanning calorimetry, polarized light microscopy, and wide‐angle X‐ray diffraction methods. Monomer 5, containing nitro groups, exhibited a smectic liquid‐crystalline phase, whereas the texture of monomer 6 without nitro groups appeared to be nematic. The PEAs containing nitro groups exhibited polymorphism (smectic and nematic), whereas those without nitro groups exhibited only one phase transition (a nematic threaded texture). The changes occurring in the phase behavior of the polymers were explained by the introduction of nitro groups. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 1289–1298, 2004 相似文献
2.
Heavy ion irradiation in the electronic stopping power region induces macroscopic dimensional change in metallic glasses and introduces magnetic anisotropy in some magnetic materials. The present work is on the irradiation study of ferromagnetic metallic glasses, where both dimensional change and modification of magnetic anisotropy are expected. Magnetic anisotropy was measured using Mössbauer spectroscopy of virgin and irradiated Fe40Ni40B20 and Fe40Ni38Mo4B18 metallic glass ribbons. 90 MeV 127I beam was used for the irradiations. Irradiation doses were 5×1013 and 7.5×1013 ions/cm2. The relative intensity ratios D 23 of the second and third lines of the Mössbauer spectra were measured to determine the magnetic anisotropy. The virgin samples of both the materials display in-plane magnetic anisotropy, i.e., the spins are oriented parallel to the ribbon plane. Irradiation is found to cause reduction in magnetic anisotropy. Near-complete randomization of magnetic moments is observed at high irradiation doses. Correlation is found between the residual stresses introduced by ion irradiation and the change in magnetic anisotropy. 相似文献
3.
Dithiocarbamate functions were incorporated into different polyacrylamide matrices crosslinked with a flexible and hydrophilic
crosslinking agent, tetraethyleneglycol diacrylate (TEGDA), and their complexation behaviours were investigated. Crosslinked
polyacrylamides with varying extents of the tetrafunctional TEGDA crosslinks were prepared by free radical solution polymerization
at 60°C using potassium persulphate as initiator in ethanol. The dithiocarbamate functionality was incorporated into these
polyacrylamides by a two-step polymer-analogous reaction involving (i)trans-amidation with ethylenediamine and (ii) dithiocarbamylation of the aminopolyacrylamide with carbon disulphide and alkali.
The complexations of dithiocarbamate with Cu(II), Ni(II), Zn(II), Co(II) and Hg(II) ions were followed under different conditions.
The metal ion intake varied with the extent of the crosslinking agent and the observed trend in complexation is Hg(II) > Cu(II)>
Zn(II)> Co(II)> Ni (II). The time-course of complexation, the possibility of recycling, swelling characteristics, and spectral
and thermal analyses were carried out. The thermal stability increases upon complexation with metal ions. 相似文献
4.
Gisha Elizabeth Luckachan C. K. S. Pillai 《Journal of polymer science. Part A, Polymer chemistry》2006,44(10):3250-3260
Novel multiblock poly(ester amide)s containing poly(L ‐lactide) and cycloaliphatic amide segments were synthesized from telechelic oligomer of α,ω‐hydroxyl terminated poly(L ‐lactide), 1,3‐cyclohexylbis(methylamine), and sebacoylchloride by the “two‐step” interfacial polycondensation method. The blocky nature of PEAs was established by FTIR and 1H NMR spectroscopies. The effect of relative content of ester and amide segments on the crystallization nature of PEAs was investigated by WAXD and DSC analyses. PEAs having lower content of PLLA, PEA 1 and PEA 2, showed a crystallization pattern analogous to polyamides, whereas PEA 3, having higher content of PLLA, showed two crystalline phases characterized by polyester and polyamide segments. Random nature of PEAs was observed from single Tg values. Biodegradation studies using the enzyme lipase from Candida Cylindracea showed higher degradation rate for PEA 3 than that for PEA 1 and PEA 2. FTIR, 1H NMR, and DSC analyses of the degraded products indicated the involvement of ester linkages in the degradation process. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3250–3260, 2006 相似文献
5.
G. R. Doshi S. N. Joshi K. C. Pillai 《Journal of Radioanalytical and Nuclear Chemistry》1991,155(2):115-127
Neutron activation analysis was used to determine129I in soil and grass samples around a reprocessing plant. The method involved wet oxidation of samples, using chromic acid, followed by distillation, collection of iodine in alkaline solution, loading on Dowex-1, irradiation and post-irradiation purification steps. The -activity of130I isotope of the purified samples was measured for quantitative determination of129I. The experimental results showed that129I and the129I/127I atomic ratio in soil samples varied from 1.09×10–4 to 5.33×10–3 pCi g–1 and 0.10×10–6 to 6.12×10–6, respectively. Further, the geometric mean of soil-to-plant transfer factor (Bv) for129I was found to be 0.16 which was comparable with other published values. 相似文献
6.
We have studied the electrocatalytic activity of RuO2-PVC film electrodes, fabricated using RuO2 powders prepared at five different temperatures, viz., 300, 400, 500, 600 and 700°C, for the oxidation of glucose in high alkaline media, 1 to 3 M NaOH. The RuO2-PVC film electrodes have been first characterized in 1 to 3 M NaOH solution by cyclic voltammetry (CV) and rotating disc electrode (RDE) techniques in a wide potential range −1,100 to 450 mV (SCE), and three redox pairs representing Ru(IV)/Ru(III), Ru(VI)/Ru(IV) and Ru(VII)/Ru(VI) transitions have been identified. The voltammetric peaks at low sweep rates have been analyzed using surface activity theory formulated for interacting electroactive adsorption sites, and interaction terms have been evaluated. The total voltammetric surface charges have been analyzed as per Trassatti’s formalism with respect to their dependence on potential sweep rate, and charges associated with less accessible and more accessible surface sites have been calculated. For glucose oxidation, the results have indicated that RuO2 (700°C)-PVC electrode shows two oxidation peaks in contrast to RuO2 (300°C)-PVC electrode. Also, RuO2 (700°C)-PVC electrode exhibits higher intrinsic electrocatalytic activity than the 300°C electrode, although the former possesses lower electrochemically active surface area. Additionally, kinetic analyses made from RDE results with reference to Michealis–Menten (MM) enzyme catalysis has shown that RuO2 (700°C) electrode possesses extended glucose-sensing range in terms of MM kinetic constant, K
M
, compared to other electrodes. Possible reasons for such differences in the behavior of the electrodes of different temperatures towards glucose oxidation are identified from studies on oxidation of glucose in solutions of different pH, oxidation of different glucose derivatives, and also from physicochemical results from BET, XRD, SEM, DTGA, XPS analysis of RuO2 powder samples. 相似文献
7.
K. J. John V. N. Rajasekharan Pillai 《Journal of polymer science. Part A, Polymer chemistry》1989,27(9):2897-2906
Crosslinked poly(4-vinylpyridine) and poly(4-vinylpyridine-co-styrene) were functionalized with permanganate group to afford the corresponding poly[4-vinyl(pyridinium permanganate)] resin. These resins were found to selectively oxidize alcohols to corresponding carbonyl compounds. These insoluble functionalized polymers possess the desired characteristics of the polymeric reagents, including operational simplicity, filterability, and regenerability. The influence of solvent, duration of reaction, and molar excess of the reagent in these oxidation reactions was investigated to find out the optimum conditions for effective oxidation reactions. The reactions were found to be more facilitated in nonpolar solvents, and a large excess of the polymeric reagent did not have any significant effect on the extent of reactions. The poly[4-vinyl(pyridinium permanganate)] resin bears a contrast to KMnO4 and other polymer-supported oxidizing agents like poly[4-vinyl(pyridinium chlorochromate)] in that it does not bring about the oxidation of the alcohol group directly attached to the ring structure. 相似文献
8.
9.
A solvent extraction separation of uranium, in the presence of thorium, cerium and lanthanides with a new calix[4]resorcinarene bearing eight hydroxamic acid groups (C4RAHA) is described. Quantitative extraction of uranium is possible in ethyl acetate solution of C4RAHA at pH 8.0. The lambda(max) and molar absorptivity (varepsilon) for uranium is 356nm and 8352Lmol(-1)cm(-1). The Binding ratio of uranium with C4RAHA as evaluated by Job's method is 4:1. The system obeys Beer's law over the range 0.075-6.0mugml(-1) of uranium with Sandell sensitivity 0.0284mugcm(-2). A preconcentration factor of 142 was achieved by directly aspirating the extract for GF-AAS measurements. The two-phase stability constant evaluated at 25 degrees C for uranium is 15.91. The complexation is characterized by favorable enthalpy and entropy changes. A liquid membrane transport study of uranium was carried out from source to the receiving phase under controlled conditions and a mechanism of transport is proposed. Uranium has been determined in standard and environmental samples. 相似文献
10.
JPC – Journal of Planar Chromatography – Modern TLC - A sensitive high-performance thin-layer chromatographic (HPTLC) method has been developed for estimation of amentoflavone, an... 相似文献