19 research outputs found
Formation of Carbonyl Sulfide by the Reaction of Carbon Monoxide and Inorganic Polysulfides
OCS formation by the reaction of inorganic polysulfides
with carbon monoxide, which are both abundant in natural
aquatic systems, was studied as a model abiotic route
for OCS formation in the dark. The net OCS accumulation
rate was a function of a bimolecular formation reaction
and simultaneous OCS hydrolysis kinetics. The reaction of
polysulfides with CO in the dark was found to be first
order with respect to CO concentration and first order with
respect to the molar sum of the polysulfide species
generated by the disproportionation of the dissolved
polysulfide precursors. The pH dependence of the OCS
production rate was controlled by the pH-dependent
disproportionation of polysulfide precursors. Lower
temperatures, intermediate redox potentials, and moderately
basic pH conditions increase the steady-state concentration
of OCS. The speciation of polysulfides in aqueous
solutions is still disputed. Some authors claim that
hexasulfide is one of the dominant species while others
believe that pentasulfide is the largest sulfide species in
aqueous systems. Despite the disagreement between different
models for speciation of polysulfides, the proposed rate
law agreed very well with the thermodynamic data based
on four and on five polysulfide species, with only minor
differences in the preexponential kinetic coefficients
Formation of carbonyl sulfide by the reaction of carbon monoxide and inorganic polysulfides
Formation of Carbonyl Sulfide by the Reaction of Carbon Monoxide and Inorganic Polysulfides
Pyrobaculum yellowstonensis Strain WP30 Respires on Elemental Sulfur and/or Arsenate in Circumneutral Sulfidic Geothermal Sediments of Yellowstone National Park
Oxygen plasma-treated gold nanoparticle-based field-effect devices as transducer structures for bio-chemical sensing
EIS (electrolyte-insulator-semiconductor) sensors based on the functionalization of uncoated gold nanoparticles supported on a Si/SiO2 structure are presented. Oxygen plasma etching at moderate power (< 200 W) provides a convenient and efficient way to remove organic capping agents from the gold nanoparticles without significant damage. Higher power intensities destroy the linkage between the SiO2 and the gold nanoparticles, and some of the gold nanoparticles are removed from the surface. The flat-band potential shift, i.e. the pH dependence of the gold-coated EIS sensors is similar (33 mV/pH) to the uncoated EIS pH-sensor. Lead, penicillin and glucose sensors were prepared by immobilization of beta-cyclodextrin, penicillinase and glucose oxidase by various immobilization techniques
