ePubs
The open archive for STFC research publications
Home
About ePubs
Content Policies
News
Help
Privacy/Cookies
Contact ePubs
Full Record Details
Persistent URL
http://purl.org/net/epubs/work/52102295
Record Status
Checked
Record Id
52102295
Title
A guide to designing graphene-philic surfactants
Contributors
T Ardyani
,
A Mohamed
,
S Abu Bakar
,
M Sagisaka
,
M Hafiz Mamat
,
M Khairul Ahmad
,
S Ibrahim
,
H Abdul Khalil
,
SM King (STFC Rutherford Appleton Lab.)
,
SE Rogers (STFC Rutherford Appleton Lab.)
,
J Eastoe
Abstract
Hypothesis: As compared to common aliphatic surfactants, increasing the number of pendant or incorporated aromatic groups in a surfactant is expected to offer significant enhancement in the affinity for graphene surfaces. The basis for enhanced graphene-philicity of aromatic surfactants is that they can develop appreciable p – p interactions with graphene. Furthermore, charged (anionic) surfactants are expected to confer electrostatic stabilization on surfactant-graphene composites. Hence, it is expected that anionic aromatic surfactants combine these two properties for effective stabilization of graphene dispersions in water. Experimental: The properties of two custom made graphene-compatible surfactants carrying two and three aromatic moieties in the hydrophobic tails, namely DC3Ph2 (sodium 1,4-dioxo-1,4-bis(3-phenylpropoxy)butane-2-sulfonate) and TC3Ph3 (sodium 1,5-dioxo-1,5-bis(3-phenylpropoxy)-3-((3-phenylpropoxy)carbonyl) pentane-2-sulfonate) were compared with other common ionic commercial surfactants. Air-water (a/w) surface tension measurements were used to assess the surfactant adsorption and inter-facial packing in the absence and presence of graphene. The surfactant coverage index for graphene (U) was calculated using surfactant headgroup areas derived from a/w surface tension data, chain volumes, and molecular fragment volumes from literature Findings: Increasing the number of aromatic groups and tails per surfactant was shown to increase the ability of surfactants to pack and fill space, as expressed by U. Comparison between the values of U for surfactants of different chain structure and architecture showed that the affinity for graphene increased with U. Hence, there is an implicit link between surfactant-graphene compatibility and the identity, chemical composition and architecture of the surfactant chains.
Organisation
ISIS
,
ISIS-LOQ
,
STFC
,
ISIS-ZOOM
Keywords
SasView
Funding Information
MOSTI
, Fundamental Research Grant Scheme (FRGS/1/2020/STG04/UPSI/02/1);
BEIS
, Newton Fund (2019-0257-103-11);
JSPS
, KAKENHI, Grant-in-Aid for Young Scientists (A) (23685034);
JSPS
, KAKENHI, Grant-in-Aid for Scientific Research (B) (26289345);
JSPS
, Fund for the Promotion of Joint International Research (Fostering Joint International Research) (15KK0221);
JSPS
, Grant-in-Aid for Challeng- ing Research (Exploratory) (17K19002);
EPSRC
(EP/I018301/1);
ANR
(13-G8ME-0003)
Related Research Object(s):
Licence Information:
Language
English (EN)
Type
Details
URI(s)
Local file(s)
Year
Journal Article
J Coll Int Sci
620 (2022): 346-355.
doi:10.1016/j.jcis.2022.03.145
2022
Showing record 1 of 1
Recent Additions
Browse Organisations
Browse Journals/Series
Login to add & manage publications and access information for OA publishing
Username:
Password:
Useful Links
Chadwick & RAL Libraries
SHERPA FACT
SHERPA RoMEO
SHERPA JULIET
Journal Checker Tool
Google Scholar