Search results for " solution"

Bitterness and astringency of flavan-3-ol monomers, dimers and trimers

1999

Intensity of astringency and bitterness of seven flavonoid compounds was evaluated by a time-intensity (TI) procedure. Eighteen trained judges rated intensity continuously from ingestion, through expectoration at 10 s until extinction of the sensation. The seven stimuli included two flavan-3-ol monomers, (+)-catechin and (−)-epicatechin, three dimers and two trimers synthesised from catechin or epicatechin by condensation with (+)-dihydroquercitin. As the degree of polymerisation increased, maximum bitterness intensity (Imax) and total duration (Ttot) decreased whereas astringency Imax increased. The monomers were significantly higher in bitterness at Imax than the dimers, which were signif…

Determining the selective impregnation of waterlogged archaeological woods with poly(ethylene) glycols mixtures by differential scanning calorimetry

2012

The differential scanning calorimetry (DSC) technique was demonstrated to be a reliable and fast tool for the investigation of the selective impregnation of archaeological woods with poly(ethylene) glycols (PEGs) mixtures. To this aim, waterlogged archaeological woods were impregnated by using aqueous mixtures of PEG 4000 and PEG 400 as well as mixtures of these polymers in the melt state. The efficiency of the treatments was also estimated by determining the total consolidant content entrapped into the cavities of degraded wood by means of DSC and thermogravimetry.

The Efficiency of Polymer Fractionation at Lower Critical Solution Temperatures

1978

The efficiency of a single fractionation step (i.e. of the partition of a given polymer sample between the coexisting phases which form when its solution demixes) is governed by the variation of the mass ratio of the individual P-mers with chain length. These dependences have been measured for the system dimethoxymethane/diethylether/ polystyrene which exhibits lower critical solution temperatures by means of the Baker-Williams method and by means of g.p.c. Their comparison with the results of previous investigation on systems showing upper critical solution temperatures reveals no thermodynamic differences in the aptitude of upper and lower critical solution temperatures for fractionation …

Cylindrical polyelectrolyte-comb-surfactant complexes

2006

Abstract Quaternized polymer combs based on poly(2-vinylpyridine-macromonomers) and the surfactant sodium dodecylsulfate are employed in the synthesis of a novel cylindrical polyelectrolyte-comb-surfactant complex (PECSC). The complex formed has 1:1 stoichiometry with respect to the ratio of dodecylsulfate to pyridinium units. It is soluble in organic solvents such as 2-butanol or chloroform. Characterization of single particle properties of the complex in organic solution is possible and yields a radius of gyration of 〈Rg〉z = 78.4 nm, a hydrodynamic radius of 〈1/Rh〉z−1 = 51.4 nm and a cross-sectional radius of Rg,cross = 3.9 nm in chloroform. The characteristic ratio γ = 〈Rg〉z/〈1/Rh〉z−1 de…

Phases and phase transitions of (NaCl)1?x(NaCN)x

1985

(NaCl)1−x(NaCN)x mixed crystals with CN-concentrationsx of 0.87, 0.76, 0.71 and 0.65 have been investigated by X-ray powder diffraction. Apart from the cubic room temperature phase, a rhombohedral and an orthorhombic phase have been identified. In addition a glass state has been observed which is characterized by a strong broadening of the cubic powder lines. The phase diagram shows a wide coexistence gap between the non-cubic phases and the glass state.

Phases and phase transitions in the mixed molecular system (NaCN)1x(KCN)x

1990

The phase diagram of (NaCN)1−x(KCN)x was examined by neutron powder diffraction in the temperature range 5K ≦T≦300 K. Several non-cubic low-temperature phases were identified for concentrationsx<xc1=0.15 andx≧xc2=0.89. Lattice parameters and ferroelastic deformations were determined from the observed powder patterns. The phase transformations were characterized following the temperature dependence of the appropriate order parameters.

Counterion-Mediated Crossing of the Cyanine Limit in Crystals and Fluid Solution: Bond Length Alternation and Spectral Broadening Unveiled by Quantum…

2020

Absorption spectra of cyanine⊕·Br⊖ salts show a remarkable solvent dependence in non/polar solvents, exhibiting narrow, sharp band shapes in dichloromethane but broad features in toluene; this chan...

1988

The unperturbed dimensions parameter KΘ is one of the most important characteristics of a polymer chain. For binary systems (polymer/solvent) and mostly for ternary systems (polymer/solvent(1)/solvent(2)) the KΘ values show large discrepancies with respect to those under thetaconditions in a single solvent. These discrepancies can be explained by considering that the interaction parameter χ (and consequently the coil dimensions or the number of intramolecular contacts between polymer segments) changes with molecular weight M. Assuming this dependency, a modified Stockmayer-Fixman equation is proposed from which a unique value of KΘ for a given polymer, independent of M, is obtained. The use…

Voltammetric behaviour of monomeric fac-trioxomolybdenum(VI) complexes with aminocarboxylic ligands in aqueous media

1992

Abstract Cyclic voltammetry, polarography and controlled-potential coulometry experiments have been used to characterize the electrochemical reduction of fac-MoO3L2− complexes (L = aspartic acid or iminodiacetic acid) in aqueous media. These complexes are reduced in two irreversible proton-assisted steps to give an oxo-bridged molybdenum(V) species and then to a molybdenum(III) dimer species. At pH 4.5, the former reduction step for the iminodiacetic acid ligand occurs at Ep = −0.75 V, while the second one appears at −1.12 V vs SCE. The overall electrochemical process can be described in terms of a homogeneous chemical reaction, coupled between two electron transfers (ECE mechanism), that i…

High-energy radiation processing, a smart approach to obtain PVP-graft-AA nanogels

2014

Abstract Poly(N-vinylpyrrolidone)-grafted-acrylic acid biocompatible nanogels (NGs) were prepared using an exiting industrial-type electron accelerator and setups, starting from semi-dilute aqueous solutions of a commercial PVP and the acrylic acid monomer. As a result, NGs with tunable size and structure can be obtained quantitatively. Sterility was also imparted at the integrated dose absorbed. The chemical structure of the NGs produced was confirmed through Fourier Transformer Infrared Spectroscopy (FT-IR). The molecular and physico-chemical properties of NGs, such as the hydrodynamic dimensions and surface charge densities, for various polymer and monomer concentrations in the irradiate…