You are not logged in.

Adhesives performance of 3-layer PE pipe coatings: effects of MAH loading, PE particles size, coating interval time and service temperature

Samsudin, M. S. F., Dell'Olio, M., Leong, K. H., Ahamid, Z. and Varley, R. J. 2016, Adhesives performance of 3-layer PE pipe coatings: effects of MAH loading, PE particles size, coating interval time and service temperature, Progress in organic coatings, vol. 99, pp. 157-165, doi: 10.1016/j.porgcoat.2016.05.013.

Attached Files
Name Description MIMEType Size Downloads

Title Adhesives performance of 3-layer PE pipe coatings: effects of MAH loading, PE particles size, coating interval time and service temperature
Author(s) Samsudin, M. S. F.
Dell'Olio, M.
Leong, K. H.
Ahamid, Z.
Varley, R. J.ORCID iD for Varley, R. J. orcid.org/0000-0002-3792-1140
Journal name Progress in organic coatings
Volume number 99
Start page 157
End page 165
Total pages 9
Publisher Elsevier
Place of publication Amsterdam, The Netherlands
Publication date 2016-10
ISSN 0300-9440
Summary Polyethylene (PE) adhesives used in combination with a PE topcoat and a fusion bonded epoxy (FBE) are one of the most common pipeline corrosion-resistant coating systems used in the oil and gas industry. The role of the adhesive in binding the topcoat to the steel surface is critical to ensuring long term protection against corrosion attack to the pipeline. Consistent with this, it is important to understand how adhesion is optimised by controlling the physical and chemical properties of the adhesive. In this work, adhesives were produced by grafting maleic anhydride (MAH) on to the polymer backbone of an inert polyethylene via free radical chemistries during reactive processing then investigating adhesive performance as function of grafting. The effects of particle size on adhesion performance were also studied for two mean particles sizes of 300 μm and 125 μm. Overall, increasing MAH (along with increasing DBP) concentration enhanced the degree of grafting, as characterised by FTIR spectroscopy, which in turn resulted in enhanced interfacial interaction between the non-polar PE topcoat and polar FBE. However, an intermediate level of MAH was found to produce the greatest adhesion due to a subsequent increase in viscosity, as shown by changes in the melt flow index (MFI) and reduced wetting of the adhesive to the primer at higher MAH concentrations. Thermal analyses using Differential Scanning Calorimetry (DSC) confirmed that functionalization of the PE adhesive disrupted its semi-crystalline structure by reducing melting temperature (Tm) and degree of crystallinity (Xc). Investigation of the effects of particle size and coating interval time revealed that finer particle sizes of ≤300 μm produced further improvement in adhesion strength compared to the coarser particles size ≥300 μm, while longer interval times degraded the adhesion performance of the coating system. This finding suggests that, apart from grafting efficiency, selection of particle size and coating times are important considerations for achieving optimum coating adhesion performance in three-layer PE coating systems.
Language eng
DOI 10.1016/j.porgcoat.2016.05.013
Field of Research 0912 Materials Engineering
0913 Mechanical Engineering
Socio Economic Objective 0 Not Applicable
HERDC Research category C1 Refereed article in a scholarly journal
ERA Research output type C Journal article
Copyright notice ©2016, Elsevier B.V
Persistent URL http://hdl.handle.net/10536/DRO/DU:30089346

Document type: Journal Article
Collection: Institute for Frontier Materials
Connect to link resolver
 
Unless expressly stated otherwise, the copyright for items in DRO is owned by the author, with all rights reserved.

Versions
Version Filter Type
Citation counts: TR Web of Science Citation Count  Cited 0 times in TR Web of Science
Scopus Citation Count Cited 0 times in Scopus
Google Scholar Search Google Scholar
Access Statistics: 28 Abstract Views, 0 File Downloads  -  Detailed Statistics
Created: Thu, 24 Nov 2016, 14:59:53 EST

Every reasonable effort has been made to ensure that permission has been obtained for items included in DRO. If you believe that your rights have been infringed by this repository, please contact drosupport@deakin.edu.au.