Mariano Iannuzzi

Prof. Mariano Iannuzzi

Curtin University, Perth, Western Australia, Australia
orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2007 in Corrosion Science
Verified
Journal Article
Open access
Mariano IannuzziMariano Iannuzzi
Mariano Iannuzzi
GFG.S. Frankel
G.S. Frankel

25 July 2017 in npj Materials Degradation
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Journal Article
Open access
PDF file
Mariano IannuzziMariano Iannuzzi
Mariano Iannuzzi
ABAfrooz Barnoush
Afrooz Barnoush
Roy JohnsenRoy Johnsen
Roy Johnsen
The ever-growing energy demand requires the exploration and the safe, profitable exploitation of unconventional reserves. The extreme environments of some of these unique prospects challenge the boundaries of traditional engineering alloys, as well as our understanding of the underlying degradation mechanisms that could lead to a failure. Despite their complexity, high-pressure and high-temperature, deep and ultra-deep, pre-salt, and Arctic reservoirs represent the most important source of innovation regarding materials technology, design methodologies, and corrosion control strategies. This paper provides an overview of trends in materials and corrosion research and development, with focus on subsea production but applicable to the entire industry. Emphasis is given to environmentally assisted cracking of high strength alloys and advanced characterization techniques based on in situ electrochemical nanoindentation and cantilever bending testing for the study of microstructure-environment interactions.

29 December 2022 in npj Materials Degradation
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Journal Article
Open access
PDF file
Mariano IannuzziMariano Iannuzzi
Mariano Iannuzzi
GFG. S. Frankel
G. S. Frankel
The monetary cost of corrosion is currently estimated at 3 to 4% of the global GDP considering direct costs exclusively. However, no study to date has quantified the environmental impact associated with steel corrosion. Here, we determined that the CO2 emissions associated with the steelmaking required to replace corroded steel will be 4.1–9.1% of the total by 2030 considering the European Union and recent U.S. greenhouse gas reduction targets. We suggest that implementing corrosion management best-practices could drastically reduce the greenhouse gas emissions associated with the replacement of corroded steel and emphasize the need for coordinated international efforts.

29 January 2013 in Journal of the Electrochemical Society
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Journal Article
Closed access
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MKMariano Kappes
Mariano Kappes
Mariano IannuzziMariano Iannuzzi
Mariano Iannuzzi
RCRicardo M. Carranza
Ricardo M. Carranza
Magnesium and magnesium alloys are susceptible to stress corrosion cracking in various environments, including distilled water. There is compelling evidence to conclude that SCC is assisted, at least in part, by hydrogen embrittlement. This paper reviews the thermodynamics of the Mg-H system and the kinetics of hydrogen transport. Aspects of magnesium corrosion relevant to hydrogen absorption are also discussed. Crack growth mechanisms based on delayed hydride cracking, hydrogen adsorption dislocation emission, hydrogen enhanced decohesion, and hydrogen enhanced localized plasticity have been proposed and evidence for each of them is reviewed herein.

1 January 2006 in Journal of the Electrochemical Society
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Journal Article
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Mariano IannuzziMariano Iannuzzi
Mariano Iannuzzi
TYT. Young
T. Young
GFG. S. Frankel
G. S. Frankel
The inhibition of Al alloy corrosion by vanadates was studied in this work. Vanadium speciation is very complicated and vital to the inhibition efficacy. Critical conditions for decavanadate polymerization from clear metavanadate solutions were investigated. Decavanadate only formed when metavanadate was added to solutions of pH 3 or less. It was not possible to change the pH of a metavanadate solution without forming decavanadates, creating an orange-colored solution. According to <mml:math display="inline"><mml:mrow><mml:mmultiscripts><mml:mi mathvariant="normal">V</mml:mi><mml:none></mml:none><mml:none></mml:none><mml:mprescripts></mml:mprescripts><mml:none></mml:none><mml:mrow><mml:mn>51</mml:mn></mml:mrow></mml:mmultiscripts></mml:mrow></mml:math>V51 nuclear magnetic resonance, monovanadates were present only in clear metavanadate solutions; orange solutions always contained decavanadates and never contained monovanadates. Orange decavanadate solutions containing <mml:math display="inline"><mml:mrow><mml:mn>0.5</mml:mn><mml:mspace width="0.3em"></mml:mspace><mml:mi mathvariant="normal">M</mml:mi><mml:mspace width="0.3em"></mml:mspace><mml:mi>NaCl</mml:mi></mml:mrow></mml:math>0.5MNaCl at pH 8.71 exhibited no significant inhibition of the oxygen reduction reaction and increasing decavanadate concentration was detrimental. In contrast, clear metavanadate solutions containing monovanadate exhibited strong inhibition of the oxygen reduction reaction, to a level similar to chromate. At a fixed pH, increased <mml:math display="inline"><mml:mrow><mml:msub><mml:mi>NaVO</mml:mi><mml:mrow><mml:mn>3</mml:mn></mml:mrow></mml:msub></mml:mrow></mml:math>NaVO3 concentration in clear metavanadate solutions increased inhibition efficiency.

1 February 2018 in International Journal of Hydrogen Energy
Verified
Journal Article
Closed access
HHHans Husby
Hans Husby
Mariano IannuzziMariano Iannuzzi
Mariano Iannuzzi
Roy JohnsenRoy Johnsen
Roy Johnsen
MKMariano Kappes
Mariano Kappes
ABAfrooz Barnoush
Afrooz Barnoush