THE TEMPERATURE DEPENDENCE OF BYTOWNITE FELDSPAR DISSOLUTION IN NEUTRAL AQUEOUS SOLUTIONS OF INORGANIC AND ORGANIC LIGANDS AT LOW TEMPERATURE (5-35°C)

dc.contributor.authorWelch S.A.
dc.contributor.authorUllman W.J.
dc.date.accessioned2021-01-23T00:52:14Z
dc.date.available2021-01-23T00:52:14Z
dc.date.issued2000
dc.description.abstractThe temperature dependence of silica release from bytownite, a Ca-Al-rich feldspar, was determined in solutions of inorganic and organic ligands at neutral pH from 5°C to 35°C. The apparent activation energy of dissolution in the inorganic (distilled water and KNO3) solutions was approximately 10 kcal/mol. The rates and temperature dependence of dissolution in acetate solutions were indistinguishable from those in the inorganic solutions. In contrast, both oxalate and gluconate enhanced the dissolution of the feldspar framework relative to the KNO3 and distilled water controls, presumably by catalyzing Al release from the mineral surface. The apparent activation energy of Si release from feldspar in the oxalate and gluconate solutions was approximately 7 kcal/mol and is due primarily to the larger enhancement of dissolution rates at low temperature. While the catalytic impact of complexing organic ligands on mineral dissolution is clear, this mechanism alone cannot be responsible for the observed biotic enhancement of weathering in field situations.
dc.identifierhttps://elibrary.ru/item.asp?id=247686
dc.identifier.citationChemical Geology, 2000, 167, 3, 337-354
dc.identifier.issn0009-2541
dc.identifier.urihttps://repository.geologyscience.ru/handle/123456789/23566
dc.subjectTEMPERATURE DEPENDENCE
dc.subjectBYTOWNITE FELDSPAR DISSOLUTION
dc.subjectLIGANDS
dc.titleTHE TEMPERATURE DEPENDENCE OF BYTOWNITE FELDSPAR DISSOLUTION IN NEUTRAL AQUEOUS SOLUTIONS OF INORGANIC AND ORGANIC LIGANDS AT LOW TEMPERATURE (5-35°C)
dc.typeСтатья

Файлы

Оригинальный пакет

Показано 1 - 1 из 1
Загрузка...
Изображение-миниатюра
Имя:
Welc_00.pdf
Размер:
277.79 KB
Формат:
Adobe Portable Document Format
Описание:

Коллекции