Search results for "solution"

Intrinsic viscosities of polyelectrolytes: specific salt effects and viscometric master curves.

2013

Dilute solutions of the sodium salt of polystyrene sulfonic acid (PSS-Na) were measured viscometrically as a function of composition in aqueous solvents of different salinity, where the extra salt was either NaCl or CaCl2. Such experiments yield {η}, the generalized intrinsic viscosities (hydrodynamic specific volume) of the polyelectrolyte for arbitrary polymer concentrations, c. In the limit of infinite dilution {η} becomes identical to the intrinsic viscosity [η]. For NaCl {η} decreases monotonously with rising c, whereas maxima are passed in the case of CaCl2. Condensing c and the concentration of extra salt in the mixed solvent into a single variable enables the establishment of predic…

Joint Aqueous Solutions of Dextran and Bovine Serum Albumin: Coexistence of Three Liquid Phases

2014

The phase diagram of the system water/dextran (DEX)/BSA was measured as well as modeled. On the experimental side, cloud points were determined and the coexisting phases were analyzed. The theoretical calculations use an approach capable of describing solutions of chain polymers and of globular proteins with the same formalism. The required thermodynamic input comes from experiments concerning the binary subsystems, except for the polymer blend for which one interaction parameter had to be adjusted. Both sources of information yield the same essential features: the existence of a large composition area of immiscibility, starting from the subsystem DEX/BSA and extending well into the region …

Palladium-Catalyzed Reaction of Boronic Acids with Chiral and Racemic ?-Bromo Sulfoxides.

2005

Palladium-catalyzed cross-coupling reactions of racemic α-bromo sulfoxides with boronic acids are carried out in either aqueous or nonaqueous medium with formation of a new C sp3−C sp2 bond. The arylation of chiral α-bromo sulfoxides occurs without racemization. The cross-coupling reaction is general and gives high yields with arylboronic acids substituted with either donor or acceptor groups but gives poor results with heteroarylboronic acids. The best yields are obtained using degassed solvents and CsF instead of aqueous base. The use of aqueous base and the presence of oxygen favor the homocoupling side reaction.

Rare Earth Metal Catalysts

2003

On the origin of functionalization in one-pot radiation synthesis of nanogels from aqueous polymer solutions

2016

Radiation-engineered poly(N-vinyl pyrrolidone) nanogels are very interesting biocompatible nanocarriers for i.v. administration of therapeutics and contrast agents for bioimaging. The manufacturing process is fast and effective, it grants excellent control of particle size and simultaneous sterilization of the formed nanogels. Interestingly, primary amino groups and carboxyl groups, useful for (bio)conjugation, are also formed in a dose-dependent fashion. In this paper, by means of both numerical simulations and experiments, the origin of nanogel size control and functionalization is investigated. This understanding offers a new dimension for the design and production of radiation-sculpture…

Atomistic Simulations of Functional Au_{144}(SR)_{60} Gold Nanoparticles in Aqueous Environment

2012

Charged monolayer-protected gold nanoparticles (AuNPs) have been studied in aqueous solution by performing atomistic molecular dynamics simulations at physiological temperature (310 K). Particular attention has been paid to electrostatic properties that modulate the formation of a complex comprised of the nanoparticle together with surrounding ions and water. We focus on Au-144 nanoparticles that comprise a nearly spherical Au core (diameter similar to 2 nm), a passivating Au-S interface, and functionalized alkanethiol chains. Cationic and anionic AuNPs have been modeled with amine and carboxyl terminal groups and Cl-/Na+ counterions, respectively. The radial distribution functions show tha…

Apparent activation energies and apparent frequency factor in polarographic waves of paludrine-Zn(II)

1993

Abstract Arrhenius and Vlcek plots of ac 1 and dp polarograms of paludrine-Zn complexes are tested in order to understand the apparent activation energies and pre-exponential factor, and their dependence on the potential. These empirical treatments are useful for obtaining information about the energetic contributions of the elemental processes associated with the Zn(II) and paludrine ligands in the overall mechanism of reduction of the complex 2:1 on the mercury interface.

Kinetic Investigation on Metal Free Anionic Polymerization of Methyl Methacrylate Using Tetraphenylphosphonium as the Counterion in Tetrahydrofuran

1997

The anionic polymerization of methyl methacrylate using tetraphenylphosphonium triphenylmethanide as an initiator proceeds in a living manner even at room temperature. The rate constants of propagation were measured between -20 and +20 °C using a flow tube reactor. At 0 °C the reaction half-lives range from 0.3 to 1 s. The polymerization follows first-order kinetics with respect to monomer conversion (with a short induction period) and shows a linear dependence of the number-average degree of polymerization on conversion with high initiator efficiencies and narrow molecular weight distributions (M w /M n < 1.1). The dependence of the measured rate constants on the active center concentratio…

Thermodynamic properties and cloud droplet activation of a series of oxo-acids

2010

Abstract. We have investigated the thermodynamic properties of four aliphatic oxo-dicarboyxlic acids identified or thought to be present in atmospheric particulate matter: oxosuccinic acid, 2-oxoglutaric acid, 3-oxoglutaric acid, and 4-oxopimelic acid. The compounds were characterized in terms of their cloud condensation nuclei (CCN) activity, vapor pressure, density, and tendency to decarboxylate in aqueous solution. We deployed a variety of experimental techniques and instruments: a CCN counter, a Tandem Differential Mobililty Analyzer (TDMA) coupled with a laminar flow-tube, and liquid chromatography/mass spectrometry (LC/MS). The presence of the oxo functional group in the α-position ca…

Selective Surface Modification of SiO2−TiO2 Supports with Phosphonic Acids

2004

The selective surface modification by phosphonic acids of SiO2−TiO2 supports at the micrometer and molecular scale was investigated. Under aqueous conditions, phosphonic acids bind to TiO2 and not to SiO2 surfaces. A micropatterned support was prepared by electron beam microlithography and selectivity, of the surface modification was evidenced using scanning Auger electron spectroscopy (SAES). The second support was a mesoporous SiO2−TiO2 mixed oxide (10 mol % Ti) epoxidation catalyst prepared by sol−gel processing. Selectivity was deduced from the decrease of the catalytic activity upon modification and from chemical analysis; bonding modes to the surface were investigated using solid-stat…