Rheopectic Behavior for Aqueous Solutions of Megamolecular Polysaccharide Sacran

The rheopectic behavior of sacran aqueous solutions, a natural giant molecular polysaccharide with a molecular weight of 1.6 × 107 g/mol, was investigated. When a low shear was applied to 1.0 wt.% sacran solution, the shear viscosity increased from 7.2 to 34 Pa·s. The increment in the viscosity was enhanced as the shear rate decreased. The shear viscosity was independent of the time at a shear rate of 0.8 s−1; simultaneously, thixotropic behavior was observed at shear rates higher than 1.0 s−1. A crossover was observed at 0.15 wt.% for the concentration dependence of both the viscosity increase and zeta potential, which was the vicinity of the helix transition concentration or gelation concentration. It was clear that the molecular mechanism for the rheopexy was different at lower and higher regions of the crossover concentration.

Conformational Transitions of Polymer Chains in Solutions Characterized by Fluorescence Resonance Energy Transfer

The critical overlap concentration C* is an important concept in polymer solutions and is defined as the boundary between dilute and semidilute regimes. In this study, the chain conformational changes of polystyrene (PS) with both high (Mn = 200,000 Da) and low (Mn = 13,000 Da) molecular weights in cis-decalin were compared by intrachain fluorescence resonance energy transfer (FRET). The random labeling of donor and acceptor chromophores strategy was employed for long PS chains, whereas chain-end labeling was used for short PS chains. By monitoring the spectroscopic intensity ratio between acceptor and donor, the concentration dependence on chain conformation from dilute to semidilute solutions was determined. Both long and short chains exhibit a conformational transition concentration, above which the polymer chains begin to collapse with concentration significantly. Interestingly, for randomly labeled polymer long chains, such concentration is consistent with C* determined from the viscosity result, below which only slight conformational change of polymer chain takes place. However, for the chain-end labeled short chain, the conformational transition concentration takes place earlier than C*, below which no significant polymer conformation change is observed.

DOMAINS OF SOLVATED IONS IN AQUEOUS SOLUTIONS, THEIR CHARACTERISTICS AND IMPACT ON ELECTRIC CONDUCTIVITY: THEORY AND EXPERIMENTAL EVIDENCE

In this paper, we identify a yet unreported, quantum-electro-dynamic (QED) interactions induced, self-organization in aqueous solutions. We show that its characteristics conform to hitherto unexplained experimental findings, reported in the literature. Specifically, our analysis shows: (a) Solvated ions may organize into micrometer (μm) sized domains, wherein the plasma oscillations of identical ions are in-phase. (b) These liquid domains have a crystalline-like lattice structure. (c) For salt solutions, for concentrations C below a solute specific transition concentration C trans , the ions organize into the "in-phase" domains. For C larger than C trans , domains form wherein the plasma oscillations of the solvated ions are just coherent. Previous studies provided theoretical and experimental evidence for the "coherent" domains. However, they did not show that the "coherent" domains only exist for C > C trans . Typically, at room temperature and pressure, C trans is about 10-4 M or below. (d) At C trans , the molar electric conductivity sharply changes, i.e. for C < C trans , the slope of the molar electric conductivity dependence on concentration is several times larger than for C > C trans .

Concentration and age-dependent elimination kinetics of polychlorinated dibenzofurans in Yucheng and Yusho patients

Half-life estimates of three polychlorodibenzofurans (PCDFs) were calculated using serial blood samples collected over a 15 to 19-year period. Blood fat PCDFs were modeled in eight individuals who were exposed to contaminated rice oil in Japan (Yusho, n = 5) and in Taiwan (Yucheng, n = 3). The elimination kinetics of PCDFs were concentration-dependent, with faster rates observed at higher concentrations and the apparent transition to slower rates occurring at about 1–3 ppb. Average half-lives of 1.1, 2.3, and 1.5 years above the transition concentration and 7.2, 5.7, and 3.5 years below it were estimated for 2,3,4,7,8-pentaCDF, 1,2,3,4,7,8-hexaCDF, and 1,2,3,4,6,7,8-heptaCDF, respectively. A positive linear correlation of half-life with age was observed for the combined group, with a rate of increase of 0.19, 0.12, and 0.05-year half-life per year of increase in age for penta-, hexa-, and hepta-CDF, respectively. The distinctly younger Yucheng patients exhibited far lower variability in half-lives and age-related trends that were quite consistent with the corresponding data on 2,3,7,8-tetrachlorodibenzo- p-dioxin (TCDD) for younger persons exposed in the Seveso incident. These age- and concentration-dependent half-lives for PCDFs may have important risk assessment implications for estimating body burdens. The current study provides limited additional evidence that PCDFs, like TCDD, are more rapidly eliminated in younger individuals.