Acido-bazické vlastnosti frakcionovaných huminových kyselin
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26310%2F08%3APU75686" target="_blank" >RIV/00216305:26310/08:PU75686 - isvavai.cz</a>
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Acid-base properties of fractionated humic acids
Popis výsledku v původním jazyce
Humic acids (HA) were fractionated by their dissolution in universal buffers (NaOH, H3BO3, H3PO4 and CH3COOH) with various pH-values. Obtained fractions were characterized by UV/VIS and FT-IR spectroscopy and their acid-base properties were studied. It was found that contain of acidic groups in majority of individual fractions is higher than the content of original HA samples. Our hypothesis is that HA structure is changed during fractionation. HA can interact with individual components of buffer and re-arranged their structure, which results in apparently higher acidity of obtained fractions. The re-arrangement of HA structure probably causes, that some acidic groups inside HA aggregates, which are not able dissociate in original HA sample, can contribute to measured acidity in individual fractions. Surprising result is that residue after dissolving original HA in very alkaline buffer (pH = 12) has after fractionation (and "exhaustion" of the largest amount of HA fraction) several tim
Název v anglickém jazyce
Acid-base properties of fractionated humic acids
Popis výsledku anglicky
Humic acids (HA) were fractionated by their dissolution in universal buffers (NaOH, H3BO3, H3PO4 and CH3COOH) with various pH-values. Obtained fractions were characterized by UV/VIS and FT-IR spectroscopy and their acid-base properties were studied. It was found that contain of acidic groups in majority of individual fractions is higher than the content of original HA samples. Our hypothesis is that HA structure is changed during fractionation. HA can interact with individual components of buffer and re-arranged their structure, which results in apparently higher acidity of obtained fractions. The re-arrangement of HA structure probably causes, that some acidic groups inside HA aggregates, which are not able dissociate in original HA sample, can contribute to measured acidity in individual fractions. Surprising result is that residue after dissolving original HA in very alkaline buffer (pH = 12) has after fractionation (and "exhaustion" of the largest amount of HA fraction) several tim
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CF - Fyzikální chemie a teoretická chemie
OECD FORD obor
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Návaznosti výsledku
Projekt
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Návaznosti
Z - Vyzkumny zamer (s odkazem do CEZ)
Ostatní
Rok uplatnění
2008
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Chemické listy
ISSN
1213-7103
e-ISSN
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Svazek periodika
102
Číslo periodika v rámci svazku
S
Stát vydavatele periodika
CZ - Česká republika
Počet stran výsledku
2
Strana od-do
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Kód UT WoS článku
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EID výsledku v databázi Scopus
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