2022
DOI: 10.15407/ujpe56.8.801
|View full text |Cite
|
Sign up to set email alerts
|

Impact of Amphiphilic Nanostructures on Formation and Rheology of Interfacial Layers and on Foam Film Drainage

Abstract: The aim of the present studies is to clarify how the surfactant adsorption layer properties are related to the course of the drainage parameters of microscopic foam films in the special case of aqueous solutions containing premicellar amphiphilic nanostructures. The scope of the research covers the adsorption dynamics, construction of equilibrium adsorption isotherms, surface rheology of interfacial layers, and foam film drainage kinetics. It is established that, in the premicellar domain, there are concentrat… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2023
2023
2023
2023

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 16 publications
0
1
0
Order By: Relevance
“…They show strong self-assembly forming various aggregate structures ranging from the nano-to the microscale and reveal desirable interfacial activity and miscellaneous phase behavior [20]. It is generally known that in the bulk aqueous phase, surfactants above their critical micellar concentration (CMC) spontaneously form aggregates, such as micelles, where hydrophobic tails are located in the micellar inner core, and the hydrophilic head groups are in contact with the aqueous phase [74]. Depending on the surfactant architecture, the shape and size of such aggregates can thus vary significantly from micelles to spheroidal micelles to vesicles to hexagonal aggregates, etc.…”
Section: Aggregation In Aqueous Solutionmentioning
confidence: 99%
“…They show strong self-assembly forming various aggregate structures ranging from the nano-to the microscale and reveal desirable interfacial activity and miscellaneous phase behavior [20]. It is generally known that in the bulk aqueous phase, surfactants above their critical micellar concentration (CMC) spontaneously form aggregates, such as micelles, where hydrophobic tails are located in the micellar inner core, and the hydrophilic head groups are in contact with the aqueous phase [74]. Depending on the surfactant architecture, the shape and size of such aggregates can thus vary significantly from micelles to spheroidal micelles to vesicles to hexagonal aggregates, etc.…”
Section: Aggregation In Aqueous Solutionmentioning
confidence: 99%