1955
DOI: 10.1021/ac60097a044
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Semimicromethod for Determination of Cyanate Ion in Presence of Interfering Substances

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Cited by 22 publications
(8 citation statements)
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“…Pathways for hydrolysis, in which the urea experiences electrophilic attack to form carbamate or carbamic acid, are generally found to be far slower in the absence of a catalyst but are acid/base-catalyzed. In water, the product ammonia may evolve or be protonated to ammonium, and the OCNH may deprotonate to cyanate, depending upon pH. In acid, cyanate is rapidly converted to ammonium and carbonic acid by eq . , …”
Section: Results and Discussionmentioning
confidence: 99%
“…Pathways for hydrolysis, in which the urea experiences electrophilic attack to form carbamate or carbamic acid, are generally found to be far slower in the absence of a catalyst but are acid/base-catalyzed. In water, the product ammonia may evolve or be protonated to ammonium, and the OCNH may deprotonate to cyanate, depending upon pH. In acid, cyanate is rapidly converted to ammonium and carbonic acid by eq . , …”
Section: Results and Discussionmentioning
confidence: 99%
“…The concentrations of ammonia and carbon dioxide in the reaction products increased over a period of several hours, indicating that they arose from the breakdown of some intermediate oxidation product. This intermediate could be adsorbed to anionic but not cationic exchange resins, was hydrolysed by 2 N-sulphuric acid and could be measured as cyanate by the method of Shaw & Bordeaux (1955).…”
Section: Resultsmentioning
confidence: 99%
“…This was measured by the indirect method of Dixon (Umbreit, Burris & Stauffer, 1959). Cyanate. This was measured as ammonia after the removal of interfering cations by ion-exchange chromatography (Shaw & Bordeaux, 1955).…”
Section: Methodsmentioning
confidence: 99%
“…16 1.2782 31.900 0.3570 35.539 0.0000 (37.9) The first equation 5 defines a quantity A', which is linear in concentration for negligible or slight association and readily extrapolates to A0; the second is the modified form of the Ostwald dilution law which neglects the higher terms in mobility involving E and J. From our earlier work4 on BU4NBPI14 in PhNOo-CCh, we obtained the result R+ = 3.55 + 15/0 (7) for the apparent hydrodynamic radius of the Bu4N + ion in this solvent system; hence we could calculate Xo+t? from the Walden-Stokes relation ,+ = Pe/1800 tn»JFt+ (8) for each of the solvent mixtures of Table I.…”
Section: Discussionmentioning
confidence: 94%