Heads or tails: Nanostructure and molecular orientations in organised erucamide surface layers.

AFM imaging Erucamide Interfacial structure Multilayers Slip additives XRR

Journal

Journal of colloid and interface science
ISSN: 1095-7103
Titre abrégé: J Colloid Interface Sci
Pays: United States
ID NLM: 0043125

Informations de publication

Date de publication:
15 May 2021
Historique:
received: 30 11 2020
revised: 26 01 2021
accepted: 27 01 2021
pubmed: 11 2 2021
medline: 11 2 2021
entrez: 10 2 2021
Statut: ppublish

Résumé

Despite the widespread industrial usage of erucamide as a slip additive to modify polymer surface properties, a controversy appears to have persisted regarding the nanostructure of erucamide surface layers, particularly the molecular orientation at the outermost layer. The erucamide nanostructure and molecular orientation, along with its surface coverage, hydrophobicity, and adhesive response, can be tuned by simply varying the erucamide concentration in the solution from which the spin coated layer is prepared. Synchrotron X-ray reflectivity (XRR) allowed a comprehensive characterisation of the out-of-plane structural parameters (e.g. molecular packing and thickness) of the erucamide layers prepared via spin coating from nonaqueous solution on silica. Complementary Atomic Force Microscopy (AFM) imaging with high lateral resolution revealed localised in-plane structures. Contact angle measurements provided information on the wettability of erucamide-coated surfaces. Peak Force Quantitative Nanomechanical Mapping (QNM) allowed a correlation between the erucamide nanostructure with the surface nanomechanical properties (i.e. adhesive response). Our results reveal erucamide surface nanostructures on silica as patchy monolayers, isolated circular bilayers/rounded rectangle-like aggregates and overlapping plate-like multilayers as the erucamide concentration in the spin coating solution was varied. In all the cases, XRR and AFM results were consistent with the picture that the erucamide tails were oriented outwards. The QNM adhesion force mapping of all the observed morphologies also supported this molecular orientation at the outermost erucamide monolayer. The wettability study further confirmed this conclusion with the observed increase in the surface hydrophobicity and coverage upon increasing erucamide concentration, with the macroscopic water contact angle θ = 92.9° ± 2.9° at the highest erucamide concentration of 2 wt%.

Identifiants

pubmed: 33567375
pii: S0021-9797(21)00106-5
doi: 10.1016/j.jcis.2021.01.087
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

506-517

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Dajana Gubała (D)

School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, UK.

Laura J Fox (LJ)

School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, UK; Bristol Centre for Functional Nanomaterials, HH Wills Physics Laboratory, University of Bristol, Bristol BS8 1TL, UK.

Robert Harniman (R)

School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, UK.

Hadeel Hussain (H)

Diamond Light Source, Diamond House, Harwell Science and Innovation Campus, Didcot, Oxfordshire OX11 0DE, UK.

Eric Robles (E)

Household Care Analytical, Procter & Gamble Newcastle Innovation Centre, Whitley Road, Longbenton, Newcastle NE12 9TS, UK.

Meng Chen (M)

Procter & Gamble Beijing Innovation Centre, 35 Yu'an Rd, Shunyi District, Beijing 101312, China.

Wuge H Briscoe (WH)

School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, UK. Electronic address: wuge.briscoe@bristol.ac.uk.

Classifications MeSH