Search results for "aqueous solution"
showing 10 items of 1610 documents
Thermodynamic Evidence of Cyclodextrin−Micelle Interactions
2002
The enthalpy of transfer (ΔHt) of hydroxypropyl-α-cyclodextrin (HP-α-CD), hydroxypropyl-β-cyclodextrin (HP-β-CD), and β-cyclodextrin (β-CD) from water to the aqueous C6F13CO2Na and C7F15CO2Na solutions were determined in the pre- and post-micellar regions. The behavior of the macrocycles is system specific. Generally, the magnitude of the enthalpy is influenced by several factors: (1) the alkyl chain length of the surfactant, (2) the cyclodextrin cavity and its alkylation, (3) the interactions between the free cyclodextrin and the free surfactant, (4) the host−guest equilibrium constant, (5) the host/guest stoichiometry, and (6) the micelle-cyclodextrin (free and/or complexed) interactions…
Chemical and pharmaceutical evaluation of the relationship between triazole linkers and pore size on cyclodextrin–calixarene nanosponges used as carr…
2016
Mixed cyclodextrin–calixarene nanosponges were used to prepare some composites with the well known polyphenolic bioactive compounds quercetin and silibinin. The composites were characterized by means of different techniques (UV-vis, FT-IR, microcalorimetry, thermogravimetry), in order to assess their loading and thermal stability. The kinetics of release of the bioactive molecules into aqueous solution were studied at two different pH values (1.0, 6.4), which mimic typical physiological conditions. Finally the possible antiproliferative effects in vitro were assayed towards three triple negative breast cancer cell lines (SUM 149, SUM 159 and MDA-MB-23). Our results point out the role assume…
Heat Capacity Study to Evidence the Interactions between Cyclodextrin and Surfactant in the Monomeric and Micellized States
2003
The heat capacities of transfer (ΔCpt) of hydroxypropyl-α-cyclodextrin and hydroxypropyl-γ-cyclodextrin (0.05 mol kg-1) from water to aqueous solutions of sodium hexanoate, sodium decanoate, and so...
Polymerization of Mono- and Bi-functional Diacetylene Derivatives in Monolayers at the Gas-Water Interface
1979
The spreading and polymerization behaviour of long chain acids and phospholipid analogues containing diacetylene groups is described. Especially the polymerization in monolayers is followed spectroscopically with a new device used in connection with a commercial UV spectrometer. The polymerization is topochemically controlled. Sonification of the phospholipid analogues in water results in the formation of liposomes with multilayered membranes. Polymerization of the liposomes in water forms aqueous solutions of polymer vesicles.
Enthalpies of Mixing of Some Primary Hydrogenated and Fluorinated Alcohols and Sodium Dodecanoate Aqueous Solutions
1993
Abstract The enthalpies of transfer from water to the surfactant solutions ΔH(W → W + S) of some hydrogenated and fiuorinated alkanols and of sodium dodecanoate NaL were determined. In the premicellar region the measurements were carried out as functions of both the additive and the surfactant concentrations in order to evaluate the interaction parameters between the additive and the surfactant molecules. It is shown that in this region, pair, triplet, and quadruplet interaction parameters between unlike solute molecules contribute to ΔH(W → W + S). Within the large uncertainty with which these parameters are determined because of the very narrow surfactant and alcohol concentration interva…
Heat capacities, volumes and solubilities of pentanol in aqueous alkyltrimethylammonium bromides
1988
Apparent molar heat capacities and volumes of pentanol, 0.05m in decyl-, tetradecyl- and hexadecyltrimethylammonium bromides micellar solutions, were measured at 25°C. They were assumed to approach the standard infinite dilution values and rationalized by means of previously reported equations following which the distribution constant between the aqueous and the micellar phase, heat capacity, and volume of pentanol in both phases are simultaneously derived. The present results show that the volume of the micellar core does not seem to have a significant effect on the apparent molar volume and heat capacity of pentanol in the micellar phase and on the free energy of transfer of pentanol from…
Conformational analysis of α,β-poly(N-hydroxyethyl)-dl-aspartamide (PHEA) and α,β-polyasparthydrazide (PAHy) polymers in aqueous solution
1998
Abstract α,β-Poly(N-hydroxyethyl)- dl -aspartamide (PHEA) and α,β-polyasparthydrazide (PAHy) are synthetic polymers previously studied for biomedical applications. We report here the results of a small-angle X-ray scattering analysis carried out on these two macromolecules in aqueous solution. The data obtained indicate that the two polymers assume remarkably different conformations in aqueous solution, although the backbone is supposed to be the same for the two chains. PHEA can be represented by a random coil conformation, whereas PAHy can be described in terms of an elliptical cylinder characterized by an almost planar structural arrangement with the backbone refolded on itself in a fash…
Adsorption of triblock copolymers and their homopolymers at laponite clay/solution interface. Role played by the copolymer nature
2009
The adsorption thermodynamics of copolymers, based on ethylene oxide (EO) and propylene oxide ( PO) units, at the laponite (RD) clay/liquid interface was determined at 298 K. The copolymer nature was tuned at molecular level by changing the hydrophilicity, the architecture and the molecular weight (Mw) keeping constant the EO/PO ratio. Polyethylene (PEGs) and polypropylene (PPGs) glycols with varying Mw and their mixture were also investigated to discriminate the role of the EO and the PO segments in the adsorption process. Enthalpies of transfer of RD, at fixed concentration, from water to the aqueous macromolecule solutions as functions of the macromolecule molality were determined. They …
Alkaline Pre-treatment of Hardwood Chips Prior to Delignification
2013
Scots pine (Pinus sylvestris) chips were pre-treated with alkaline solutions (alkali charges of 1, 2, 3, 4, 6, and 8% of NaOH on the oven-dried wood material) at 130°C and 150°C for various treatment times (30, 60, 90, and 120 minutes). Under these conditions, 2.0–13.6% of the wood d.s. was dissolved into the aqueous hydrolysates. The soluble organic fraction was primarily characterized in terms of carbohydrates (monosaccharides and oligo-/polysaccharides) and their alkali-catalyzed degradation products: aliphatic carboxylic acids containing, besides non-volatile hydroxy carboxylic acids, volatile formic and acetic acids. With increasing alkali charge, temperature, and time, the enhanced fo…
Influence of some aromatic and aliphatic compounds on the rate of photodegradation of phenol in aqueous suspensions of TiO2
1995
Abstract The influence of 3-nitrophenol, 4-nitrophenol, pentachlorophenol, ethanol, 2-propanol, ethanoic acid and ethanedioic acid on the photodegradation rate of phenol in an aqueous suspension of TiO2 (anatase) irradiated in the near-UV region was investigated. Binary mixtures of organic compound and phenol in molar ratios of 1:1 and 10:1 were used for the photoreactivity experiments performed in a batch reactor. The mineralization rate of all the mixtures was also monitored by measuring the total organic carbon (TOC) concentration. The reactivity results indicate that the photodegradation rate of phenol is mainly determined by the total amount of aromatic substrates present in the reacti…