Protein-iron interaction using cyclic voltammetry

Across all industries, companies are continuously searching for methods to increase productivity and to save costs by reducing machine downtime and maintaining equipment at high standards. In marine and offshore industries specifically, significant amount of downtime cases occur because of metal str...

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Main Author: Saiful Irfan Mohamed Bajuri
Other Authors: Matteo Seita
Format: Final Year Project
Language:English
Published: 2019
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Online Access:http://hdl.handle.net/10356/77376
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-773762023-03-04T19:19:31Z Protein-iron interaction using cyclic voltammetry Saiful Irfan Mohamed Bajuri Matteo Seita School of Mechanical and Aerospace Engineering DRNTU::Engineering::Mechanical engineering Across all industries, companies are continuously searching for methods to increase productivity and to save costs by reducing machine downtime and maintaining equipment at high standards. In marine and offshore industries specifically, significant amount of downtime cases occur because of metal structural failure due to corrosion, when there is a possible interaction between a protein and metal. Most of these metal structures contain iron. However, due to the complexity of any protein based reaction, phenomenon of protein-iron is generally still poorly understood. Herein, the author uses an electrochemical set up called Cyclic Voltammetry to quantify any kind of favourable protein-iron interaction. A commonly investigated protein, lysozyme was used. This report documents the effects of changing the following variables: scan rate ranging from 100mV/s to 250mV/s, scan limit, presence of degassing, concentration of metal, concentration of protein, and type of electrodes used from glassy carbon (GC), gold, edge plane pyrolytic graphite (EPPG) electrodes as they may affect protein-iron interaction. The results show that cathodic and anodic peaks in CV were observed using EPPG electrode due to its high sensitivity, but no conclusive results were detected using GC and gold electrodes. CV of FeCl added to lysozyme (when FeCl is limiting in quantity) indicated higher current peaks when compared with the respective FeCl control solution, whereas CV shape of FeCl in excess to lysozyme showed a similar graph to FeCl control solution. A faster scan rate of 250mV/s also showed clearer peaks compared to slower scan rates of 100mV/s. Based on these key findings and improvement that could be done on the work, the authors have suggested future work that could shed light into the poorly understood phenomenon: protein induced corrosion (PIC). Bachelor of Engineering (Mechanical Engineering) 2019-05-28T01:49:04Z 2019-05-28T01:49:04Z 2019 Final Year Project (FYP) http://hdl.handle.net/10356/77376 en Nanyang Technological University 42 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Engineering::Mechanical engineering
spellingShingle DRNTU::Engineering::Mechanical engineering
Saiful Irfan Mohamed Bajuri
Protein-iron interaction using cyclic voltammetry
description Across all industries, companies are continuously searching for methods to increase productivity and to save costs by reducing machine downtime and maintaining equipment at high standards. In marine and offshore industries specifically, significant amount of downtime cases occur because of metal structural failure due to corrosion, when there is a possible interaction between a protein and metal. Most of these metal structures contain iron. However, due to the complexity of any protein based reaction, phenomenon of protein-iron is generally still poorly understood. Herein, the author uses an electrochemical set up called Cyclic Voltammetry to quantify any kind of favourable protein-iron interaction. A commonly investigated protein, lysozyme was used. This report documents the effects of changing the following variables: scan rate ranging from 100mV/s to 250mV/s, scan limit, presence of degassing, concentration of metal, concentration of protein, and type of electrodes used from glassy carbon (GC), gold, edge plane pyrolytic graphite (EPPG) electrodes as they may affect protein-iron interaction. The results show that cathodic and anodic peaks in CV were observed using EPPG electrode due to its high sensitivity, but no conclusive results were detected using GC and gold electrodes. CV of FeCl added to lysozyme (when FeCl is limiting in quantity) indicated higher current peaks when compared with the respective FeCl control solution, whereas CV shape of FeCl in excess to lysozyme showed a similar graph to FeCl control solution. A faster scan rate of 250mV/s also showed clearer peaks compared to slower scan rates of 100mV/s. Based on these key findings and improvement that could be done on the work, the authors have suggested future work that could shed light into the poorly understood phenomenon: protein induced corrosion (PIC).
author2 Matteo Seita
author_facet Matteo Seita
Saiful Irfan Mohamed Bajuri
format Final Year Project
author Saiful Irfan Mohamed Bajuri
author_sort Saiful Irfan Mohamed Bajuri
title Protein-iron interaction using cyclic voltammetry
title_short Protein-iron interaction using cyclic voltammetry
title_full Protein-iron interaction using cyclic voltammetry
title_fullStr Protein-iron interaction using cyclic voltammetry
title_full_unstemmed Protein-iron interaction using cyclic voltammetry
title_sort protein-iron interaction using cyclic voltammetry
publishDate 2019
url http://hdl.handle.net/10356/77376
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