BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Department of Theoretical Physics - ECPv6.5.1.5//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-ORIGINAL-URL:https://web-f1.ijs.si
X-WR-CALDESC:Events for Department of Theoretical Physics
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:Europe/Ljubljana
BEGIN:DAYLIGHT
TZOFFSETFROM:+0100
TZOFFSETTO:+0200
TZNAME:CEST
DTSTART:20260329T010000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:+0200
TZOFFSETTO:+0100
TZNAME:CET
DTSTART:20261025T010000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Europe/Ljubljana:20261008T140000
DTEND;TZID=Europe/Ljubljana:20261008T150000
DTSTAMP:20261006T012432
CREATED:20261004T085033Z
LAST-MODIFIED:20261005T202131Z
UID:109089-1791468000-1791471600@web-f1.ijs.si
SUMMARY:Fabio Staniscia\, "Surfactant exchange kinetics at the air-water interface"
DESCRIPTION:Surfactants continuously exchange between bulk solution and interfaces. This process governs dynamic interfacial properties such as time-dependent surface tension\, foam stability\, and wetting. While equilibrium adsorption isotherms are routinely measured\, the underlying desorption kinetics remain difficult to access experimentally\, especially for fast-exchanging\, low-molecular-weight surfactants. Here we use molecular dynamics simulations to quantify the residence times of short-chain alcohols at the air-water interface. We find that residence times increase exponentially with alkyl chain length and with surface coverage. Furthermore\, we show that the residence time scales linearly with the adsorption coefficient\, linking equilibrium binding affinity to kinetic persistence.\nhttps://indico.ijs.si/event/4179/
URL:https://web-f1.ijs.si/event/fabio-staniscia-surfactant-exchange-kinetics-at-the-air-water-interface/
LOCATION:C/2-X – F1 čajnica (Jamova)
END:VEVENT
END:VCALENDAR