Potentiometric investigation of the oxidation of ferrous chloride by oxygen
Effect of various catalyzers, hydrochloric acid, and iron chloride concentrations on oxidation rate of bivalent iron ions at room temperature
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Effect of various catalyzers, hydrochloric acid, and iron chloride concentrations on oxidation rate of bivalent iron ions at room temperature
Conversion of 2-formyl dienone III into dienone IV upon irradiation in acetic acid followed by base-catalyzed deformylation of crude photoproduct
Analytical study of catalyzed hydrazine decomposition reaction chambers for predicting system steady state and transient behavior
Computer program representing two dimensional steady state model of distributed-feed catalyzed hydrazine decomposition reaction chamber
Mathematical model and computer program of catalyzed hydrazine decomposition reaction chamber
The susceptibility of the decomposition of the tosylhydrazones of simple carbonyl compounds to changes in the proton-donating ability (protonicity) of the solvent have long been known, but only recently has the mechaninistic path of this reaction been explored in detail. The nature of the products in tosylhydrazone decomposition (and thus by inference the nature of the intermediates) has been found to depend on (1) the protonicity of the solvent, (2) the concentration of the base, and (3) the nature of the cation association with the base. in recent deuterium-labelling studies on the base-catalyzed decomposition of the tosylhydrazones of cyclopropanecarboxaldehyde (I), norbornan-2-one (II), and camphor (III), evidence has accumulated for the existence of two distinct paths involving a "carbonic" and a "cationic" intermediate in this reaction depending on the reaction conditions. Present evidence indicates that the observed products from tosylchydrazone decomposition arise from either a carbene or a diazonium salt, generated from an intermediate diazo compound. In the absence of a Lewis acid, there is no present evidence to support a carbonium ion as an intermediate in the protonic decomposition of tosylhydrazones.
Weight savings advantage of catalyzed hydrogen rocket propellant, discussing specific impulse and tankage volume
Polymerization of ITP and CTP into rIC copolymer containing IMP and CMP in alternating sequence catalyzed by Azotobacter vinelandii RNA polymerase
Catalyzed hydrazine decomposition reaction chamber
Properties, relative magnitudes and relationship of pyrophosphate exchange reactions catalyzed by DNA polymerase from Escherichia colis
Programs manual for one-dimensional and two- dimensional steady state models of catalyzed hydrazine decomposition reaction chambers
Alternating copolymer of guanylic and cytidylic residues synthesized in RNA polymerase-catalyzed reaction
ADP-ATP catalyzed exchange reaction in turtle bladder microsomes, using chromatographic measurements of conversion rates
Computer programming manual for calculating temperature and reactant concentrations as functions of time and axial position in catalyzed continuous flow hydrogen-oxygen reactors
Epoxy novolac resin-cured alicyclic anhydride amine-catalyzed ablative polymers molecular structure from computer correlation of analytical data
Continuous processes for enzymatic production of carbohydrates from glucose are discussed. Key reactant in process is identified as phosphorylase which catalyzes reversible formation or degradation of polysaccharide. Chemical compounds and reactions to synthesize polysaccharides are analyzed.
The PC8B-4 fuel cell electrical power supply is an electrical powerplant designed to convert the chemical reaction of hydrogen and oxygen into electrical energy. It utilizes catalyzed electrodes with a potassium hydroxide electrolyte. The powerplant and test stand control unit are described together with a specifications summary. Separate sections deal with: performance, reactants supply and control, heat removal, water removal instrumentation, operation, and safety considerations.
Twenty-eight crystalline salts were X-irradiated and treated with an ammoniacal nickel hypophosphite solution. Treatment (development) of six of the salts resulted in precipitation of nickel metal. The developable salts were four hypophosphites, sodium phosphite, and nickel formate. A mechanism is proposed for the process based on the postulate that micro amounts of hydrogen atoms are formed during the radiation step. During development, these hydrogen atoms cause the formation of nucleation sites of nickel metal. In turn, these sites catalyze further reduction of the nickel cations by the hypophosphite. The results are discussed in terms of application of the process to the formation of developable latent images.