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The roles of CO2 and water vapour on the high temperature corrosion of a type 430 stainless steel as an interconnect of bio-gas fuel intermediate temperature SOFCs
(2025-12-01)
Thublaor, Thammaporn
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Srihathai, Padungaut
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Tengprasert, Watcharapon
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Suparapinyopapkul, Grid
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Yan, Jiayi
A Type 430 stainless steel was exposed to Ar-20 %CO<inf>2</inf> without and with water vapour at 800 °C up to 96 h. Increasing water vapour content from 5 % to 40 % helped reduce mass gain, enhance volatilisation, and improve scale adhesion with fewer pores at scale/steel interface. Mechanisms for Cr and Mn volatilisations including the direct reactions between Cr-containing oxide and CO<inf>2</inf> were suggested with the aid of the XPS results. Mathematical relations that express the role of water vapour on concentrations of defects responsible for scale growth were proposed to help explain the reduced oxidation rate.
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Oxidation and Scale Adhesion of a Type 430 Stainless Steel in Ar–CO2 Gas Mixtures at 800 °C
(2023-04-01)
Wiman, Panya
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Muengjai, Angkana
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Srihathai, Padungaut
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Thublaor, Thammaporn
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Siripongsakul, Thamrongsin
Biogas is an alternative source of fuel potentially used to run solid oxide fuel cells (SOFCs). It mainly consists of CH<inf>4</inf> and CO<inf>2</inf> which can degrade the SOFC interconnect, which is typically made of stainless steel. To investigate the effect of each gas constituent, we focussed here on the effect of CO<inf>2</inf> on high-temperature oxidation behavior of and scale adhesion on the stainless steel interconnect, Type 430 stainless steel. The samples studied were oxidised in CO<inf>2</inf> at contents of 5–100% at 800 °C. The oxidation kinetics were found to be parabolic with the rate constant increasing when the CO<inf>2</inf> content increased. The scale adhesion was assessed using a tensile-test method. The scale formed in the atmosphere containing higher CO<inf>2</inf> content exhibited poorer scale adhesion, as indicated by a lower strain initiating the first spallation and a larger spallation percentage after the first spallation took place. The worsened scale adhesion relates to pores formed at the scale/steel interface. The adhesion energies were further quantified giving the values of about 40–100 J m–2. Oxidation mechanisms were suggested based on the dependence of the parabolic rate constant on the oxygen partial pressure and the inward diffusion of carbon-bearing species.
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Comparative study on liquefaction behaviors of xylan hemicellulose as treated by different hydrothermal methods
(2020-02-01)
Phaiboonsilpa, Natthanon
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Champreda, Verawat
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Laosiripojana, Navadol
Liquefaction behaviors of xylan were studied as treated by six different hydrothermal methods. As a comparative study, a xylan sample isolated from corn core was subjected to hot-compressed water, hot-compressed 0.01 and 0.1wt% H<inf>2</inf>O<inf>2</inf> solutions under pressurization of N<inf>2</inf> or CO<inf>2</inf> at 110–250 °C for 0 min in 10-ml batch-type reactor. Not only xylose and xylo-oligosaccharides, but also arabinose, glucose, and acetic acid were recovered as hydrolyzed products. In addition, decomposition compounds, i.e. furans and organic acids were found. The highest xylose yield could be attained at 210 °C in all the studied hydrothermal methods, except for only 0.1wt% H<inf>2</inf>O<inf>2</inf> solution under pressurization of CO<inf>2</inf>. By this strongly oxidative condition, where peroxy carbonic acid was formed in situ, the temperature that xylose could be highly recovered was at 190 °C. The highest xylose yield of 61.62wt% was obtained by 0.01wt% H<inf>2</inf>O<inf>2</inf> solution under pressurization of N<inf>2</inf>. Formation of furan compounds showed a preference to the treatments with pressurized CO<inf>2</inf>, while organic acids had a better recovery when N<inf>2</inf> was applied. Different results in the production of various liquefied products could be attributed to the degree of hydrolysis and oxidation reactions which altered under the different hydrothermal methods.
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Modeling and optimization of proton-conducting solid oxide electrolysis cell: Conversion of CO2 into value-added products
(2016-11-01)
Namwong, Lawit
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Authayanun, Suthida
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Saebea, Dang
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Patcharavorachot, Yaneeporn
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Arpornwichanop, Amornchai
Proton-conducting solid oxide electrolysis cells (SOEC-H+) are a promising technology that can utilize carbon dioxide to produce syngas. In this work, a detailed electrochemical model was developed to predict the behavior of SOEC-H+ and to prove the assumption that the syngas is produced through a reversible water gas-shift (RWGS) reaction. The simulation results obtained from the model, which took into account all of the cell voltage losses (i.e., ohmic, activation, and concentration losses), were validated using experimental data to evaluate the unknown parameters. The developed model was employed to examine the structural and operational parameters. It is found that the cathode-supported SOEC-H+ is the best configuration because it requires the lowest cell potential. SOEC-H+ operated favorably at high temperatures and low pressures. Furthermore, the simulation results revealed that the optimal S/C molar ratio for syngas production, which can be used for methanol synthesis, is approximately 3.9 (at a constant temperature and pressure). The SOEC-H+ was optimized using a response surface methodology, which was used to determine the optimal operating conditions to minimize the cell potential and maximize the carbon dioxide flow rate.
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A low-cost method for determination of calcium carbonate in cement by membraneless vaporization with capacitively coupled contactless conductivity detection
(2010-05-15)
Sereenonchai, Kamonthip
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Teerasong, Saowapak
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Chan-Eam, Sumonmarn
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Saetear, Phoonthawee
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Choengchan, Nathawut
This work presents a flow analysis method for direct quantitation of calcium carbonate in cement without pretreatment of the sample. The method is based on online vaporization of CO<inf>2</inf> gas following acidification of the sample inside a small chamber that has a flow of acceptor solution passing around it. Solubilization of the CO<inf>2</inf> gas into the acceptor stream changes the conductivity of the acceptor solution causing an increase of signal at the capacitively coupled contactless conductivity detection (C4D) placed at the outlet of the vaporization chamber. This chamber is an adaption from previous work reported on 'membraneless vaporization' (MBL-VP). The method can be used in the quality control of production of mixed cement. These cement materials usually have calcium carbonate contents at high concentration range (e.g., 33-99% (w/w) CaCO<inf>3</inf>). Analysis of samples by this method is direct and convenient as it requires no sample pretreatment. The method is low-cost with satisfactory accuracy and acceptable precision. © 2010 Elsevier B.V.
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