Search results for "Concentration."
showing 10 items of 1849 documents
Influence of the pH on the behavior of an imprinted polymeric stationary phase--supporting evidence for a binding site model.
2001
The equilibrium isotherms of the two enantiomers of phenylalanine anilide (PA) were measured by conventional frontal analysis at three different pH on a thermally-treated imprinted stationary phase selective for the L enantiomer. The first of these pH (buffer pH=3.0, pH(app)=4.0) is well below the apparent pKa (6.4) of the two solutes, the second (buffer pH=5.8, pH(app)=7.0) slightly below this pKa, and the third (buffer pH=7.0, pH(app)=8.3) well above it. The experimental data were fitted to several isotherm models. The best estimates of the parameters of these models are reported and discussed. The corresponding isotherms are compared with the experimental ones. The contributions of the e…
The second component of human complement: Detection of two hemolytic forms in plasma by pH Variation
1988
The second component of human complement (C2) in pseudoglobulin prepared from normal plasma eluted as a single peak at high conductivity (30 mS) and pH 4.5 from the cationic exchangers S-Sepharose or Mono S in the Fast Protein Liquid Chromatography (FPLC) System. The C2 was stable at pH 4.5 and 0 degrees C if enzyme inhibitors were used and the pH was raised to 6.0 after elution from the columns. After rechromatography on Mono S in the FPLC System at the median isoelectric point of 5.5 or pH 6.0, the C2 eluted as two distinct hemolytic forms: the first peaked at 16 mS, the second at 30 mS. The two forms of C2 did not correlate with the allotypic variant of C2 in individual, normal human pla…
Modeling of Amino Acid Electrodiffusion through Fixed Charge Membranes
2001
Abstract We study theoretically the electrodiffusion of amino acids through fixed charge membranes, calculating the ionic fractions of the amino acid in the membrane as well as its total flux as a function of the relevant experimental parameters (amino acid concentration, salt concentration, and pH of the external solution; membrane fixed charge concentration; and amino acid membrane/solution partition coefficients) under different experimental conditions (symport vs antiport transport, uphill transport, etc.). The theoretical approach employed is based on the Nernst–Planck flux equations in the (Goldman) constant electric field assumption and considers all the species present in the system…
Solvent quality as reflected in concentration- and temperature-dependent Flory-Huggins interaction parameters
2001
Flory-Huggins interaction parameters (χ) between poly(dimethylsiloxane) (weight-average molecular weight = 152 kg/mol) and various solvents (methyl ethyl ketone, toluene and n-octane) were determined as a function of composition and temperature with vapor-pressure measurements. These data, complemented by independent information for dilute and very concentrated solutions, serve as the basis for a discussion of solvent quality via different theoretical relations. Regardless of polymer concentration, the χ values fall from methyl ethyl ketone via toluene to n-octane, the ketone being the worst solvent and the hydrocarbon being the best solvent. The variation of χ with composition and temperat…
Maximum exposure levels for xylene, formaldehyde and acetaldehyde in cars.
2004
Although millions of individuals are exposed to emissions from articles inside cars, relatively little has been published about possible adverse health effects and about exposure levels that can be considered safe or "acceptable". Xylene, formaldehyde and acetaldehyde represent typical examples of relevant volatile organic substances (VOC) released from articles inside cars. Recently, a concept for derivation of maximum exposure levels for volatile organic substances in cars has been published. In the present study we applied this concept to derive maximum exposure levels for xylene, formaldehyde and acetaldehyde and compared the resulting concentrations to exposure levels usually found ins…
Hierarchical structure formation of cylindrical brush polymer-surfactant complexes.
2009
The complex formation of cylindrical brush polymers with poly(l-lysine) side chains (PLL) and sodium dodecyl sulfate (SDS) can induce a helical conformation of the cylindrical brush polymer in aqueous solution (Gunari, N.; Cong, Y.; Zhang, B.; Fischer, K.; Janshoff, A.; Schmidt, M. Macromol. Rapid Commun. 2008, 29, 821-825). Herein, we have systematically investigated the influence of surfactant, salt, and pH on the supramolecular structure formation. The cylindrical brush polymers and their complexes with surfactants were directly visualized by atomic force microscopy in air and in aqueous solution. The alkyl chain length (measured by the carbon number, n) of the surfactant plays a key rol…
Optical tweezing electrophoresis of isolated, highly charged colloidal spheres
2001
Abstract We report on a novel optical tweezing experiment measuring the electrophoretic mobility μ of highly charged spherical particles suspended in water at volume fractions Φ≤2×10 −7 . At deionised conditions μ =2.5×10 −8 m 2 V −1 s −1 , it decreases further upon increasing the salt concentration c . We compare our data to measurements at larger Φ, where generally much larger μ and a qualitatively different dependence on the salt concentration are observed. To characterise the dependence on Φ we performed measurements at no added salt. There the mobility increases in the unordered state but stays constant at μ =6.8×10 −8 m 2 V −1 s −1 as the system develops fluid order. In the ordered re…
Sequence-specific and DNA structure-dependent interactions of Escherichia coli MutS and human p53 with DNA
2013
Many proteins involved in DNA repair systems interact with DNA that has structure altered from the typical B-form helix. Using magnetic beads to immobilize DNAs containing various types of structures, we evaluated the in vitro binding activities of two well-characterized DNA repair proteins, Escherichia coli MutS and human p53. E. coli MutS bound to double-stranded DNAs, with higher affinity for a G/T mismatch compared to a G/A mismatch and highest affinity for larger non-B-DNA structures. E. coli MutS bound best to DNA between pH 6 and 9. Experiments discriminated between modes of p53-DNA binding, and increasing ionic strength reduced p53 binding to nonspecific double-stranded DNA, but had…
CO2 as a C1-organic building block: Electrocarboxylation of aromatic ketones. A quantitative study of the effect of the concentration of substrate an…
2006
The purpose of this work is to establish and discuss quantitative relationships between the selectivity in preparative scale electrolysis and intrinsic and operational parameters for the electrocarboxylation of aromatic ketones. For the investigated ketones, under appopriate experimental conditions the selectivity of the process is mainly determined by the competition between carboxylation and protonation, de-halogenation reactions (when an halogenated ketone is involved), and possibly dimerizations involving the electrogenerated radical anion. A simple model was proposed to account for these unwanted side paths which allows to predict the dependence of the selectivity as a function of the …
Behaviour of modified and unmodified polybutadienes in the semidilute regime
1997
Abstract The association behaviour of polybutadiene modified with 4-phenyl-l,2,4-triazoline-3,5-dione was studied in semidilute solution through static (SLS) and dynamic light scattering (DLS). The results were compared with the unmodified polybutadiene, whose behavior in semidilute solution was also studied as function of the molecular weight. At higher concentrations a small-angle excess scattering in SLS and a slow mode motion in DLS were observed both for modified and unmodified polybutadienes suggesting the presence of large clusters. Increasing the polymer concentration, the mass fraction of the slow motion increases up to values near 1, indicating a proximity to the gel point. For po…