TY - JOUR
T1 - Bubble formation in water with addition of a hydrophobic solute
AU - Okamoto, Ryuichi
AU - Onuki, Akira
N1 - Funding Information:
This work was supported by KAKENHI No. 25610122. RO acknowledges support from the Grant-in-Aid for Scientific Research on Innovative Areas ?Fluctuation and Structure? from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.
Publisher Copyright:
© 2015, EDP Sciences, SIF, Springer-Verlag Berlin Heidelberg.
PY - 2015/7/1
Y1 - 2015/7/1
N2 - Abstract: We show that phase separation can occur in a one-component liquid outside its coexistence curve (CX) with addition of a small amount of a solute. The solute concentration at the transition decreases with increasing the difference of the solvation chemical potential between liquid and gas. As a typical bubble-forming solute, we consider O2 in ambient liquid water, which exhibits mild hydrophobicity and its critical temperature is lower than that of water. Such a solute can be expelled from the liquid to form gaseous domains while the surrounding liquid pressure is higher than the saturated vapor pressure pcx. This solute-induced bubble formation is a first-order transition in bulk and on a partially dried wall, while a gas film grows continuously on a completely dried wall. We set up a bubble free energy ΔG for bulk and surface bubbles with a small volume fraction ϕ. It becomes a function of the bubble radius R under the Laplace pressure balance. Then, for sufficiently large solute densities above a threshold, ΔG exhibits a local maximum at a critical radius and a minimum at an equilibrium radius. We also examine solute-induced nucleation taking place outside CX, where bubbles larger than the critical radius grow until attainment of equilibrium. Graphical abstract: [Figure not available: see fulltext.]
AB - Abstract: We show that phase separation can occur in a one-component liquid outside its coexistence curve (CX) with addition of a small amount of a solute. The solute concentration at the transition decreases with increasing the difference of the solvation chemical potential between liquid and gas. As a typical bubble-forming solute, we consider O2 in ambient liquid water, which exhibits mild hydrophobicity and its critical temperature is lower than that of water. Such a solute can be expelled from the liquid to form gaseous domains while the surrounding liquid pressure is higher than the saturated vapor pressure pcx. This solute-induced bubble formation is a first-order transition in bulk and on a partially dried wall, while a gas film grows continuously on a completely dried wall. We set up a bubble free energy ΔG for bulk and surface bubbles with a small volume fraction ϕ. It becomes a function of the bubble radius R under the Laplace pressure balance. Then, for sufficiently large solute densities above a threshold, ΔG exhibits a local maximum at a critical radius and a minimum at an equilibrium radius. We also examine solute-induced nucleation taking place outside CX, where bubbles larger than the critical radius grow until attainment of equilibrium. Graphical abstract: [Figure not available: see fulltext.]
KW - Flowing Matter: Liquids and Complex Fluids
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U2 - 10.1140/epje/i2015-15072-9
DO - 10.1140/epje/i2015-15072-9
M3 - Article
AN - SCOPUS:84956931781
SN - 1292-8941
VL - 38
SP - 1
EP - 12
JO - European Physical Journal E
JF - European Physical Journal E
IS - 7
M1 - 72
ER -