Nitrite-Induced Activation of Iodate into Molecular Iodine in Frozen Solution
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F19%3A00113352" target="_blank" >RIV/00216224:14310/19:00113352 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1021/acs.est.8b06638" target="_blank" >http://dx.doi.org/10.1021/acs.est.8b06638</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acs.est.8b06638" target="_blank" >10.1021/acs.est.8b06638</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Nitrite-Induced Activation of Iodate into Molecular Iodine in Frozen Solution
Popis výsledku v původním jazyce
A new mechanism for the abiotic production of molecular iodine (I-2) from iodate (IO3-), which is the most abundant iodine species, in dark conditions was identified and investigated. The production of I-2 in aqueous solution containing IO3- and nitrite (NO2-) at 25 degrees C was negligible. However, the redox chemical reaction between IO3- and NO2- rapidly proceeded in frozen solution at -20 degrees C, which resulted in the production of I-2, I-, and NO3-. The rapid redox chemical reaction between IO3- and NO2- in frozen solution is ascribed to the accumulation of IO3-, NO2-, and protons in the liquid regions between ice crystals during freezing (freeze concentration effect). This freeze concentration effect was verified by confocal Raman microscopy for the solute concentration and UV-visible absorption spectroscopy with cresol red (acid-base indicator) for the proton concentration. The freezing-induced production of I-2 in the presence of IO3- and NO2- was observed under various conditions, which suggests this abiotic process for I-2 production is not restricted to a specific region and occurs in many cold regions. NO2--induced activation of IO3- to I-2 in frozen solution may help explain why the measured values of iodine are larger than the modeled values in some polar areas.
Název v anglickém jazyce
Nitrite-Induced Activation of Iodate into Molecular Iodine in Frozen Solution
Popis výsledku anglicky
A new mechanism for the abiotic production of molecular iodine (I-2) from iodate (IO3-), which is the most abundant iodine species, in dark conditions was identified and investigated. The production of I-2 in aqueous solution containing IO3- and nitrite (NO2-) at 25 degrees C was negligible. However, the redox chemical reaction between IO3- and NO2- rapidly proceeded in frozen solution at -20 degrees C, which resulted in the production of I-2, I-, and NO3-. The rapid redox chemical reaction between IO3- and NO2- in frozen solution is ascribed to the accumulation of IO3-, NO2-, and protons in the liquid regions between ice crystals during freezing (freeze concentration effect). This freeze concentration effect was verified by confocal Raman microscopy for the solute concentration and UV-visible absorption spectroscopy with cresol red (acid-base indicator) for the proton concentration. The freezing-induced production of I-2 in the presence of IO3- and NO2- was observed under various conditions, which suggests this abiotic process for I-2 production is not restricted to a specific region and occurs in many cold regions. NO2--induced activation of IO3- to I-2 in frozen solution may help explain why the measured values of iodine are larger than the modeled values in some polar areas.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
20800 - Environmental biotechnology
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2019
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
ENVIRONMENTAL SCIENCE & TECHNOLOGY
ISSN
0013-936X
e-ISSN
—
Svazek periodika
53
Číslo periodika v rámci svazku
9
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
9
Strana od-do
4892-4900
Kód UT WoS článku
000467641800025
EID výsledku v databázi Scopus
2-s2.0-85064838026