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DTSTAMP:20250125T184819
UID:8fddee96-db44-11ef-a655-000e0c3db68b
SUMMARY:ICP Kolloquium: Prof. Dr. Thomas Palberg
DESCRIPTION:In deionized water CO 2 forms carbonic acid which partially dissociates. Such ’realistic’ salt free systems contain a significant background electrolyte concentration and a pH of 5.5. Both lowers the effective charge of dielectric surfaces. Surprisingly, the remaining molecular CO 2 causes an additional drastic decharging effect, even to complete decharging in water equilibrated against pure CO 2 . Molecular CO 2 acts directly on the degree of dissociation and thus lowers the bare charge, while effective charges merely follow suit. MD simulations show the formation of a diffusely adsorbed monolayer of CO 2 , which locally lowers the dielectric constant. Based on this we suggested dielectric charge regulation as novel decharging mechanism. If then salts are added to the carbonized surfaces, one finds recharging by co-ion adsorption. This process is favoured by hydrophobicity, by co-ion size and, most important, also by the amount of adsorbed CO 2 . Given the ubiquity of dielectric surfaces in contact with aqueous electrolytes, this very general charge regulation processes appear to be of great fundamental and practical importance.
DTSTART;TZID=Europe/Berlin;VALUE=DATE:20250223
LOCATION:ICP, Seminarraum , 1.079, Allmandring 3, 
URL;VALUE=URI:https://www.icp.uni-stuttgart.de/news/events/ICP-Kolloquium-Prof.-Dr.-Thomas-Palberg/
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