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81.
Patricia M. Nassar Rose M.Z.Georgetto Naal Silvia H. de Pauli João B.S. Bonilha Laura T. Okano Frank H. Quina 《Journal of colloid and interface science》1997,190(2):461
In aqueous solution, the interaction between sodium dodecyl sulfate (SDS) and poly(ethylene glycol) (PEG) results in the formation of small aggregates or clusters of SDS attached to the PEG polymer chain. Selectivity coefficients for exchange of two monovalent (N-methyl-4-cyanopyridinium cation and Tl+) and two divalent (methylviologen cation and Cu2+) counterions at the surface of SDS–PEG clusters, determined employing photophysical techniques, are similar, but not identical, to those for exchange at the surface of SDS micelles in the absence of PEG. The principal factor affecting ion exchange selectivity in SDS–PEG clusters does not appear to be aggregate size or surface charge density but rather the presence of poly(oxyethylene) subunits at the aggregate surface. 相似文献
82.
G. Papanastasiou A. Papoutsis M. Tsirtou I. Ziogas 《Journal of solution chemistry》1996,25(2):203-217
The kinetics of the reaction between sodium ethoxide and methyl iodide has been studied at 25°C in various cyclohexane-ethanol solvent mixtures with a cyclohexane content of 10 to 50% per volume. The determination of the rate constants att=0 were carried out by a new iterative method proposed in this investigation. The obtained results show that the reaction rate decreases with the increasing cyclohexane content. This behavior can be attributed to various solute-solvent interactions of electrostatic nature. On the other hand, the variation of ion and ion pairs rate constants with solvent composition permits the various solvation effects to be taken into account. 相似文献
83.
84.
Five of the six possible aqueous two-salt mixtures from among NaCl, KCl, NaH2PO4,and KH2PO4 have been studied by the isopiestic method at 25°C. The sixth mixture, NaCl–KCl, has been studied previously. The deviations from ideal mixing behavior are described by a series of coefficients which were found by regression analysis. The coefficients were used to calculate the excess Gibbs energies of mixing for equal ionic strength fractions of each salt and the trace activity coefficient of each salt at an ionic strength of 2 mode-kg–1. The cross-square mixing rule is obeyed within experimental uncertainty for the excess Gibbs energies of mixing. 相似文献
85.
86.
The exces enthalpies of solution of some primary and secondary alcohols in aqueous sodium dodecylsulfate micellar solutions were measured and the results were explained by considering the distribution of alcohols between aqueous and micellar phases. The distribution constant and the enthalpy of transfer (and the standard free energy and entropy of transfer) were obtained. The thermodynamic parameters for the transfer of secondary alcohols from the aqueous to the sodium dodecylsulfate (NaDS) micellar phase differ slightly from those of the corresponding primary alcohols. For both series of alcohols the additivity rule holds for free energies of transfer whereas enthalpies and entropies display convex curves. The present data are compared to those for the transfer of the same solutes from the aqueous to the dodecyldimethylamine oxide (DDAO) and dodecyltrimethylammonium bromide (DTAB) micellar phases. The role of the hydrophilic interactions between the OH group and the micelles' head groups is formulated. The thermodynamics of the branched methyl group were determined. Furthermore, the thermodynamics of solvation of primary alcohols in water, in NaDS micelles, and in octane have been calculated using reference states based on the assumption that the empty space around alcohols in the initial and final states is the same. It is shown that the solvation of alcohols in NaDS micellar phase is enthalpy driven and that the thermodynamic properties of solvation vs. the length of the alcohol tail is the same for water and NaDS micelles whereas it is different for octane. A possible explanation for this difference is that the alkyl chain of alcohols folds in octane. 相似文献
87.
以1,4-二氯丁烷和硫化钠为原料,碘为催化剂,乙醇为溶剂合成了四氢噻吩。最佳反应条件:1,4-二氯丁烷50 mmol,n(1,4-二氯丁烷)∶n(硫化钠)=1.0∶1.3,碘10 mg,回流反应3 h时,产率91.79%,纯度≥99%(GC)。 相似文献
88.
Thereza Christina Vessoni Penna Marina Ishii Adalberto Pessoa Junior Laura de Oliveira Nascimento Luciana Cambricoli de Souza Olivia Cholewa 《Applied biochemistry and biotechnology》2004,114(1-3):453-468
To determine the influence of various culture conditions, transformed cells of Escherichia coli expressing recombinant green fluorescent protein (GFPuv) were grown in nine cultures with four variable conditions (storage
of inoculated broth at 4°C prior to incubation, agitation speed, isopropyl-β-d-thiogalactopyranoside [IPTG] concentration, and induction time). The pelleted cells were resuspended in extraction buffer
and subjected to the three-phase partitioning (TPP) extraction method. To determine the most appropriate purification resin,
protein extracts were eluted through one of four types of HiTrap hydrophobic interaction chromatography (HIC) columns prepacked
with methyl, butyl, octyl, or phenyl resins and analyzed further on a 12% sodium dodecylsulfatepolyacrylamidegel. With Coomassie
staining, a single band between 27 (standard GFPuv) and 29 kDa (molecular weight standard) was visualized for every HIC column
sample. TPP extraction with HIC elution provided about 90% of the GFPuv recovered and eight-fold GFPuv enrichment related
to the specific mass. Rotary speed and IPTG concentration showed, respectively, greater negative and positive influences on
GFPuv expression at the beginning of the logarithmic phase for the set culture conditions (37°C, 24-h incubation). 相似文献
89.
Transmission electron microscopy of freeze fractured and replicated samples (TEM) and polarizing light microscopy (PLM) are
used to investigate the defect structures of the thermotropic and lyotropic mesophases of the non-steroidal antiinflammatory
drug fenoprofen sodium and of the thermotropic mesophase of the nonionic surfactant sucrose oleate (O1570). All mesophases
have a layered, smectic structure. The thermotropic liquid crystal of feno-profen sodium is an interdigitated smectic A phase
(smectic Ad) having the highest viscosity of the investigated samples. The thermotropic mesophase of the sugar ester is also
of the type smectic A, likely to be of subtype smectic A2 (bilayered smectic structure). The lyotropic mesophase is of lamellar
liquid crystalline nature and has a much lower viscosity than the thermotropic mesophases. In the PLM the lyotropic fenoprofen
mesophase has a strong tendency to form a pseudoisotropic texture, indicating a strong tendency to form undisturbed layered
structures. Other textures exhibited in the PLM are fan-shaped texture and maltese-cross texture. Confocal domains, cylinders,
pits and peaks as well as screw dislocations are found in great number in the TEM. However, no greater regions of undisturbed
lamellar arrangement in the lyotropic mesophase could be detected. The only texture of the thermotropic fenoprofen mesophase
visible in the PLM is the fan-shaped texture, indicating confocal domains as predominant structural elements. However, no
confocal domains (tori or Dupin cyclides) are found in the TEM. In the PLM the sugar–ester mesophase exhibited a fan-shaped
texture, maltese crosses and oily streaks as dominant textures. In the TEM only a few +π and −π disclinations and imperfect
confocal domains could be detected. The discrepancies in the appearance of defect structures and textures between the mesophases
as well as the discrepancies in the findings in the PLM and in the TEM investigations are caused by the different sample preparation
and the different viscosities of the mesophases.
Received: 28 May 1997 Accepted: 2 September 1997 相似文献
90.
钯-8-羟基喹啉-5-磺酸络合物电极反应和十二烷基硫酸钠的增敏机理 总被引:1,自引:0,他引:1
钯 8 羟基喹啉 5 磺酸形成的络合物的峰电流 (pH 8.6 ,- 0 .6 8V)具有吸附特性 ,为不可逆电极反应过程。其电子转移数 (n)、电子转移系数 (α)及饱和吸附量 (Γs)分别为 2、0 .4 6和 2 .2× 10 - 9mol cm2 ;钯 与8 羟基喹啉 5 磺酸的络合比为 1∶2 ;稳定常数 (K)为 8.73× 10 7。加入阴离子表面活性剂十二烷基硫酸钠未形成三元络合物 ,催化电流是由与十二烷基硫酸钠共吸附在电极表面上的超氧阴离子自由基氧化了络合物的电极反应中间体所产生的。 相似文献