Search results for "Relative"

Mean square radius of gyration and hydrodynamic radius of jointed star (dumbbell) and H-comb polymers

1996

Equations for the mean square radius of gyration and the hydrodynamic radius for jointed stars (dumbbells) and H-combs are derived, based on random flight statistics for each subchain. Comparision with literature data on computer simulations and experimental data for H-combs show good agreement for the g-value of the mean square radius of gyration even in good solvents. This suggests that for the mean square radius of gyration the relative dimension of a H-comb relative to the linear molecule of the same degree of polymerization is not altered significantly by long range interactions, as in the case of star polymers. For the hydrodynamic radius the situation is different. Fair agreement is …

Polyelectrolytes Revisited: Reliable Determination of Intrinsic Viscosities

2007

The linear extrapolation of (hh0)/(h0c) towards c !0 constitutes the basis of traditional methods to determine intrinsic viscosities (h), where h is the viscosity of polymer solutions of concentration c and h0 is the viscosity of the pure solvent. With uncharged macromolecules this procedure works well; for polyelectrolytes it fails because of the pronounced non-linearity of the above dependence at high dilution resulting from the increasing electrostatic inter- actions. This contribution presents a new method for the determination of (h). It rests upon the application of the laws of phenomenological thermodynamics to the viscosity of polymer solutions and introduces a generalized intrinsic…

1985

Viscosity measurements were carried out as a function of pressure and temperature with solutions of 8 wt.-% PVC (Mw ≈ 75 000) in ten thermodynamically good solvents by means of a Searle-type viscometer. A rollingxyhball viscometer was used for the investigation of the pure solvents. In all cases the viscosity increases in a more or less exponential manner when the pressure is raised. The viscosity ratio f1000 = η1000 bar/η1bar can be varied by the choice of the solvent from ca. 2 (tetrahydrofuran) to 3,0 (cyclohexanone) at 40°C. For a constant temperature of 40°C, the volumes of activation for the viscous flow of the solutions, V≠, or f1000 exceed that of the pure solvent, by typically 25%.…

Temporal fatty acid profiles of human decomposition fluid in soil

2017

Abstract We studied the changes in concentration and relative abundance of human-derived fatty acids (FAs) in soil over a period of one year. The study is based on analysis of soil underneath a human body that lay on the soil surface for 18 days before it was discovered. Soil samples were taken when the body was removed, and also 358 days later. Large amounts of the total FA concentration at the start of the measurement period were still present one year after the removal of the body. The FA profile suggested that extensive saturated FA reduction occurred during the first 18 days after deposition. 10-Hydroxystearic acid and FA salts, which are characteristic of adipocere, were abundant in a…

Viscometric behaviour of polymer blends based on poly (vinylidene fluoride)

1994

The viscosity behaviour of dilute dimethylformamide solutions of poly(vinylidene fluoride)-poly (methyl methacrylate) and poly(vinylidene fluoride)-polystyrene has been studied at 25°C. The polymer concentration ranges are such that neither phase separation nor microgel formation occurs, although we are very close to theta conditions. The intrinsic viscosity and viscosity interaction parameter of the ternary mixtures have been calculated. The estimation of the compatibility of the above polymer pairs has been studied based on: a) specific viscosities; b) viscosity interaction parameters, according to Krigbaum and Wall formalism, and c) viscosity interaction parameters of a system formed by …

1979

Pressure influences on the viscosity of polymer solutions

1982

Of all physico-chemical quantities characterizing the behavior of liquids, the viscosity coefficient η is normally most sensitive to pressure. Early measurements of η(p) date back almost 100 years [1] but they were carried out with very different objectives [2]. Currently, one is particularly interested in polymer solutions, for instance because of the additives to motor oils and of oil recovery. The present paper reports on measurements with polystyrenes of high molecular uniformity in eight different solvents. It confines itself to zero-shear viscosities and discusses the possibilities of discovering the influence of pressure via the molecular structure of the solvent and via its thermody…

Temperature influence on moisture transfer through synthetic films

2000

Abstract Water transfer through films was investigated as a function of the temperature, the physical state of water and the relative humidity (RH) difference. The films were two synthetic packagings: a hydrophobic one, the polyethylene, a hydrophilic one, the cellophane. Some phenomena which could occur at low temperatures were discussed, such as polymer structure change due to mechanical relaxation or network plasticisation and modification of the penetrant diffusion at its melting temperature. But it seems that the comparison of water permeabilities (WPs) with temperature, especially at subzero temperatures, requires the correction of their calculation with the difference of water chemic…

Données expérimentales et modélisation d’adsorption des systèmes N2(g)/montmorillonite potassique de Camp-Berteau et N2(g)/hydrotalcite carbonatée

1999

Resume In this paper capacities of adsorption of nitrogen onto two clays at 77 K are compared and analyzed. One system is a montmorillonite of Camp-Berteau saturated by potassium cation and the second one is an hydrotalcite saturated by carbonate anion. Adsorbed amounts have been obtained using a volumetric technique. So it is shown that the smectite adsorbed more than the hydrotalcite at the same relative pressure of nitrogen. The modelling of experimental data by various theories of adsorption as de Brunauer, Emmett et Teller (BET) and t-method are used to calculate the specific surface and to have access to the porosity of these materials at 77 K. Then it is shown that the adsorption of …

Water Adsorption Characteristics of Acyclic Oligosaccharides of α-Gluose Studied by Near Infrared Spectroscopy

2013

The adsorption properties of water molecules on maltooligosaccharides are attributed to the OH groups of the glucose rings in maltooligosaccharides. The water molecules are adsorbed onto OH groups by hydrogen bond formation. Near infrared spectroscopic and gravimetric techniques were used in analysing the adsorption characteristics of maltooligosaccharides. Near infrared spectra of the dry maltooligosaccharides were acquired during the adsorption of wa- ter molecules at a relative humidity of 50%. The amounts of water adsorbed by the samples were also recorded by an ana- lytical balance. Second derivative techniques were used in decomposing the OH combination frequency of the adsorbed water…