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Article

Analysis and Prediction of Corrosion of Refractory Materials by Potassium during Biomass Combustion-Thermodynamic Study

1
National Engineering Laboratory for Biomass Power Generation Equipment, School of the Renewable Energy, North China Electric Power University, Beijing 102206, China
2
Department of Mechanical and Material Engineering, Queen’s University, Kingston, ON K7L 3N6, Canada
3
State Grid Energy Conservation Services CO., Ltd., Beijing 100056, China
*
Author to whom correspondence should be addressed.
Materials 2018, 11(12), 2584; https://doi.org/10.3390/ma11122584
Submission received: 9 November 2018 / Revised: 4 December 2018 / Accepted: 15 December 2018 / Published: 18 December 2018
(This article belongs to the Section Corrosion)

Abstract

:
As a kind of renewable resource, biomass has been used more and more widely, but the potassium contained in biomass can cause corrosion of the refractory. For a better understanding of corrosion thermodynamic mechanisms, the five components of common refractory materials (magnesium chrome spinel MgO·Cr2O3, magnesium aluminum spinel MgO·Al2O3, Al2O3, MgO, and Cr2O3) with potassium salts (K2CO3, K2SO4, and KCl) under high-temperature were studied by using the FactSageTM 7.0 software. Thermodynamic calculation results indicate that MgO is the best corrosion resistance of the five components of refractory materials. Based on the obtained results, the corrosion experiments in the laboratory were carried out (muffle furnace or high-temperature tube furnace) for corrosion reaction of KCl and MgO. The chemical compositions of the corroded samples were analyzed by X-ray diffraction (XRD). Under laboratory conditions (600–1200 °C), no corrosion products have been observed in the high-temperature corrosion experiments. The result indicates that to prevent the corrosion processes, refractories should contain as much MgO as possible.

1. Introduction

The total amount of biomass accumulated in the world every year is equivalent to 10 times of the total energy consumption of the year. Biomass is the fourth energy after coal, oil, and natural gas, and contributes 14% to the world’s primary energy consumption [1,2]. Biomass has the characteristic of near-zero carbon dioxide emissions. Therefore, the development and utilization of biomass energy is an important way to optimize energy structure, alleviate the contradiction between energy supply and demand, protect the environment and reduce greenhouse gas emissions. As one of the important renewable energy sources, biomass energy occupies an important position in energy system [3]. In recent years, China has accelerated the adjustment of its energy structure, actively promoted the development and utilization of biomass energy, and biomass power generation has been flourishing. In coal K primarily exists in the format of feldspar (K2O·Al2O3·6SiO2) while the content of activated K species (e.g., K2SO4, KCl, K2CO3) is negligible [4,5]. However, it is very different in biomass. As it has a very high ratio of oxygen, a part of potassium is combined with a strong oxygen-containing functional group, and some other parts are present in the inner mineral or combined with the organic functional group. Since the potassium content of biomass is much higher than that of coal, high levels of potassium compounds, especially potassium chloride, can cause severe corrosion of boilers during combustion.
Many studies have focused on the mechanism of potassium release during biomass combustion/gasification/pyrolysis [6,7,8,9]. J. M. Johansen et al. [10] reported that Cl was the main facilitator for K release through sublimation of KCl at the reaction temperature above 700–800 °C. H. Kassman et al. [11] also reported that Cl could facilitate the release of K by the formation of KCl (g) in the biomass combustion at high temperatures. In addition, the ash agglomeration behavior caused by potassium during biomass combustion/pyrolysis/gasification is also the focus of researchers [12,13,14,15]. H. Zhan et al. [16] suggested that coal ash is a potential additive for not only fixing potassium, but also increasing the temperatures of biomass ash fusion. The effect of potassium compounds on the corrosion of equipment in biomass is mainly focused on the superheater metal materials [17,18,19,20]. Nevertheless, up to now, only a few researches have focused on the mechanism of corrosion of refractory by biomass ash [21]. It is very limited that there are thermodynamic studies on the corrosion of refractory by active potassium in biomass combustion are limited.
Since the corrosion behavior of potassium on refractories during biomass combustion is greatly affected by temperature and potassium salt type, this study mainly investigates different combustion temperatures (600, 700, 800, 900, 1000, 1100, and 1200 °C). Different kinds of active potassium (K2CO3, K2SO4, and KCl) corrode five components of common refractory materials (magnesium chrome spinel MgO·Cr2O3, magnesium aluminum spinel MgO·Al2O3, Al2O3, MgO, and Cr2O3). The FactSageTM 7.0 software was used to simulate the interaction of the five components with three kinds of potassium salts based on the established calculation model and predict the phase formation when thermodynamic equilibrium was reached. The Gibbs free energy of each reaction under different conditions are calculated by using the FactSageTM 7.0 software. We systematically analyzed the possibility of reacting five components of common refractory materials with three kinds of potassium salts and the mineral phase of corrosion products. We obtained the direction and limit of reaction in the multi-reaction system of refractory by potassium corrosion process and the affection of corrosion by temperature and potassium salt type. The goal of this paper is to provide guidance for the selection and optimization of biomass boiler refractories.

2. Thermodynamic Calculations

Thermodynamic calculations were carried out using the version 7.0 of the FactSage™ software package (GTT Technologies, Aachen, Germany and Thermfact/CRCT, Montreal, QC, Canada), because it is one of the largest fully integrated databases in the field of chemical thermodynamics. FactSage™ 7.0 software contains several thermodynamic databases, including a database of FactPS (the FactSage™ 7.0 contains 6872 kinds of compounds) evaluation and optimization of hundreds of metal solutions, oxide liquid phase and solid phase solutions, hydrazine, molten salt, aqueous solutions and other solution databases. The FactSage™ software is based on the system’s minimum Gibbs free energy and provides information on the phases formed, their proportions and composition, the individual activities of each chemical component, and the thermodynamic properties of various compositions, pressures, and temperatures [22]. Therefore, FactSage™ software can conduct the thermodynamic calculation of the corrosion of refractory by potassium salt. In this study, the Equilib module was used which is adapted to multi-component systems like potassium compounds and refractory materials.
In this paper, three kinds of oxide components commonly used in refractories and two kinds of spinels synthesized by them are selected as research objects. The three oxides are Al2O3, MgO, and Cr2O3, and the two spinels are MgO·Cr2O3 and MgO·Al2O3. In order to investigate the corrosion mechanism of potassium compounds on the five components of refractory materials, three potassium salts K2CO3, K2SO4, and KCl were selected. This is because active potassium is present in the solid and gas phases in the form of these three potassium salts during biomass combustion.
1 mol of the five components of refractory materials and three potassium salts were used as input data for the calculation. The Equilib module was used to calculate the change of Gibbs free energy in the corrosion of five components of refractory materials by three potassium salts. The trend of reaction was analyzed. The larger the negative value of Gibbs free energy, the greater the reaction trend. Moreover, corrosion products at different temperatures were obtained, and the chemical reaction equations that may occur during the corrosion process were inferred. All simulations were performed with temperatures varying from 600 to 1200 °C in steps of 100 °C at 1 atm pressure.

3. Thermodynamic Experimental Procedure

A total of three sets of experiments were performed at different temperatures, 600, 1000, and 1200 °C. The corrosion test at 600 °C is controlled by a control box type muffle furnace (GW-300C China Coal Research Institute, Beijing, China). Since the maximum temperature of the muffle furnace is less than 1000 °C, the corrosion experiments at 1000 °C and 1200 °C were performed by high-temperature tube furnace (TF-1700C Beijing MeiCheng Scientific Instrument Co., Ltd., Beijing, China). Control box type resistance muffle furnace, with a double furnace ceramic fiber structure and a modular control system, can automatically raise temperature and maintain the constant temperature, and has accurate stable and reliable temperature control. The high-temperature tube furnace adopts a high-temperature corundum tube, and the temperature can be controlled by the temperature controller, which allows the temperature to vary between room temperature and 1700 °C.
KCl and MgO samples (molar ratio of 1) were placed in muffle furnace or high-temperature tube furnace. After warming to a specified temperature, the furnace stayed in standby mode for 4 h. When the experiment was completed and the tube furnace was cooled to room temperature, experiment reaction products were analyzed by XRD (Shimadzu, Kyoto, Japan) and Jade 5.0 software (Materials Data Ltd., Livermore, CA, USA).

4. Results and Discussion

4.1. Corrosion Reaction of K2CO3 and the Five Components of Refractory Materials

As can be seen from Figure 1, in the range of 600 to 1200 °C, the Gibbs free energy of the reactions between each of the five components of refractory materials and K2CO3 are all negative. The Gibbs free energy becomes more negative gradually with the increasing of the temperature which indicates that the higher the temperature, the greater the tendency of the refractory to be corroded by K2CO3.
Corrosion products and reaction equations of K2CO3 reacting with five components of refractory materials are shown in Table 1. It can be seen from Table 1 that the two oxides (Al2O3 and Cr2O3) and the two spinels are corroded by potassium carbonate at 600 °C. The reactions in which Cr2O3 and MgO·Cr2O3 are corroded by K2CO3 at 600–1200 °C are
K2CO3 + 1/2 Cr2O3 + 3/4O2 = K2CrO4 + CO2
K2CO3 + 1/2 MgO·Cr2O3 + 3/4O2 = 1/2MgO + K2CrO4 + CO2
The reaction product of Al2O3 and MgO·Al2O3 corroded by K2CO3 and the degree of reaction are related to temperature. At 600 °C, 0.3416 mol of Al2O3 is corroded by K2CO3 to form K2 Al12O19 through reaction (3), and 0.6584 mol of Al2O3 is corroded by K2CO3 to form KAlO2 through reaction (4). At 700–1200 °C, Al2O3 is corroded by K2CO3 through reaction (4), and 1 mol of Al2O3 is completely corroded to form 2 mol of KAlO2.
The two reactions in which Al2O3 is corroded by K2CO3 are
K2CO3 + 6Al2O3 = K2Al12O19 + CO2
K2CO3 + Al2O3 = 2KAlO2 + CO2
At 600 °C, only 0.0608 mol of MgO·Al2O3 is corroded to form KAlO2 and MgO, while at 700–1200 °C, 1 mol of MgO·Al2O3 is completely corroded, as described by reactions (5).
K2CO3 + MgO·Al2O3 = 2KAlO2 + MgO + CO2
Furthermore, it can be seen from the table that the amount of corrosion products in which MgO reacted with K2CO3 is less than 10−4 mol. However, it can be seen from Figure 1 that the Gibbs free energy of the reaction between K2CO3 and MgO is negative. This is because the calculation results of FactSageTM 7.0 showed that K2CO3 will decompose at 600–1200 °C to produce KO2, K2O2, and K2O. This explains why the Gibbs free energy of MgO reacts with K2CO3 is negative. Therefore, MgO is the best corrosion resistance of the five components of refractory materials.

4.2. Corrosion Reaction of K2SO4 and the Five Components of Refractory Materials

It can be seen from Figure 2 that the tendency of Gibbs free energy change of the five components of refractory materials reacted with K2SO4 in the range of 600 to 1200 °C is consistent with the one of reactions between the five components of refractory materials and K2CO3. Two spinels (MgO·Cr2O3 and MgO·Al2O3) are more strongly corroded by K2SO4, while MgO has the least tendency to be corroded by K2SO4.
From Table 2, we can find that at 600–900 °C, the five components of refractory materials are not corroded by K2SO4. However, when the temperature further increased to 1000 °C, a small amount of Cr2O3 (0.0001 mol) is corroded by K2SO4 to form K2CrO4. As the temperature increases, more Cr2O3 is corroded by K2SO4 through reactions (6)
K2SO4 + 1/2 Cr2O3 + 3/4O2 = K2CrO4 + SO3
Similarly, when the temperature rises to 1100 °C, 0.004 mol of Al2O3 and 0.00005 mol of MgO·Cr2O3 are corroded by K2SO4 to form KAl9O14 and K2CrO4, respectively. As the temperature increases, more Al2O3 and MgO·Cr2O3 are corroded by K2SO4, and the reactions of Al2O3 and MgO·Cr2O3 by K2SO4 are
K2SO4 + 9Al2O3 = 2KAl9O14 + SO3
K2SO4 + 1/2 MgO·Cr2O3 + 3/4O2 = K2CrO4 + 1/2MgO + SO3
It can also be seen from the table that the amount of corrosion products in which MgO or MgO·Al2O3 reacted with K2SO4 is less than 10−4 mol.
In summary, Cr2O3 is most susceptible to be corroded by K2SO4, followed by Al2O3 and MgO·Cr2O3, while MgO and MgO·Al2O3 are the most difficult ones to be corroded by K2SO4.

4.3. Corrosion Reaction of KCl and the Five Components of Refractory Materials

As can be seen from Figure 3, in the range of 600–1200 °C, the tendency of Gibbs free energy change of the five components of refractory materials reacted with KCl is consistent with the one of the reactions between the five components of refractory material and K2CO3 or K2SO4.
It can be seen from Table 3 that at 600–900 °C, the five components of refractory materials are not corroded by KCl. However, when the temperature further increased to 1000 °C, a small amount of Al2O3 (0.0009 mol) and Cr2O3 (0.00015 mol) are corroded by KCl to form KAl9O14 and K2CrO4, respectively. The increase in temperature causes more Al2O3 and Cr2O3 to be corroded by KCl. The reaction equations are
2KCl + 9Al2O3 + 1/2O2 = 2KAl9O14 + Cl2
4KCl + Cr2O3 + 5/2O2 = 2K2CrO4 + 2Cl2
When the temperature rises to 1100 °C, 0.00005 mol of MgO·Cr2O3 is corroded by KCl to form K2CrO4, and the reaction of MgO·Cr2O3 by KCl is
4KCl + MgO·Cr2O3 + 5/2O2 = 2K2CrO4 + MgO + 2Cl2
It can also be seen from the table that the amount of corrosion products in which MgO or MgO·Al2O3 reacted with KCl is less than 10−4 mol.
In summary, Al2O3 and Cr2O3 are most susceptible to corrosion by KCl, followed by MgO·Cr2O3, and MgO and MgO·Al2O3 are the most difficult to be corroded by KCl.
It is worth noting that, as can be seen from Figure 1, Figure 2 and Figure 3, the Gibbs free energy of MgO·Al2O3 reacting with the three potassium salts is the smallest. However, it can be seen from the corrosion products calculated from FactSageTM 7.0 that MgO·Al2O3 is the least susceptible to potassium salt in the five refractory components except MgO. This also shows that the reaction tendency of the corrosion reaction is the only one that can be obtained by calculating the Gibbs free energy. The estimation of difficulty of the corrosion reaction needs to be obtained by considering the products of Table 1, Table 2 and Table 3 regarding the corrosion of the refractory component by the potassium salts.

4.4. Thermodynamic Experiment

As can be seen from the results calculated by the FactSageTM 7.0 software, MgO has the best corrosion resistance and is most suitable for refractory materials resistant to potassium salt corrosion. KCl is the most abundant potassium salt in biomass combustion process, so it is necessary to investigate the thermodynamic experiment of corrosion of MgO by KCl.
Figure 4 shows the XRD spectra of samples after the test of high temperature corrosion of KCl and MgO at three temperatures of 600, 1000, and 1200 °C. As can be seen from the figure, only MgO and KCl are detected in the sample at the temperatures of 600 °C and 1000 °C, and no new substance is formed. Only MgO is detected in the sample at the temperature of 1200 °C, which is consistent with the results from the modulation by Factsage software. Under the condition of high temperature 1200 °C, KCl is in the form of gas. It shows that MgO has good resistance to KCl corrosion at 1200 °C, which is consistent with the results calculated by FactSageTM 7.0 software (see Table 3).

5. Conclusions

From the viewpoint of thermodynamics, this study focused on the Gibbs free energy and the mineral phase of corrosion products of potassium salts corrosion to the five components of refractory materials using thermodynamic calculation method. According to the calculation results, corrosion experiments in the 600–1200 °C temperature range were carried out.
From the calculation results using FactSageTM 7.0 software, it can be found that the MgO has the best resistance to the potassium salts corrosion, followed by MgO·Al2O3 and MgO·Cr2O3, and Al2O3 and Cr2O3 have the worst resistance to the potassium salts corrosion. The new phases were KAlO2 and K2Al12O19 which appeared as the result of chemical reaction between Al2O3 and K2CO3, while Al2O3 reacts with K2CO3 or KCl to form KAl9O14. K2CrO4 was also a new phase in Cr2O3 or MgO·Cr2O3 as the product of the reaction with the three potassium salts. No corrosion products were found in the reaction of MgO with the three potassium salts. Finally, the results obtained from the FactSageTM 7.0 calculations agrees with XRD analysis. The negative effects of corrosion problems caused by potassium salt can be limited by using refractories contained as much MgO as possible.

Author Contributions

Conceptualization, Y.Z., G.C., and C.D.; Software, Y.Z.; Validation, Y.Z. and L.L.; Formal Analysis, Y.Z., G.C., and L.L.; Investigation, Y.Z., J.Z. and L.L.; Resources, Y.Z. and C.D.; Data Curation, Y.Z., L.L., and F.L.; Writing—Original Draft Preparation, Y.Z., F.L., and G.C.; Writing—Review and Editing, Y.Z., X.W., and G.C.; Visualization, Y.Z. and G.C.; Supervision, Y.Z. and C.D.; Project Administration, Y.Z. and G.C.; Funding Acquisition, Y.Z. and J.Z.

Funding

This work was financially supported by the Fundamental Research Funds for the Central Universities (2016MS54, 2018ZD08, 2018MS038), National Natural Science Foundation of China (51306054), National Basic Research Program of China (2015CB251501), and State Grid Science and Technology Program (No. SGJN0000ASJS1700136).

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Gibbs free energy of the reaction between K2CO3 and the five components of refractory materials in the 600–1200 °C temperature range.
Figure 1. Gibbs free energy of the reaction between K2CO3 and the five components of refractory materials in the 600–1200 °C temperature range.
Materials 11 02584 g001
Figure 2. Gibbs free energy of the reaction between K2SO4 and the five components of refractory materials in the 600–1200 °C temperature range.
Figure 2. Gibbs free energy of the reaction between K2SO4 and the five components of refractory materials in the 600–1200 °C temperature range.
Materials 11 02584 g002
Figure 3. Gibbs free energy of the reaction between KCl and the five components of refractory materials in the 600–1200 °C temperature range.
Figure 3. Gibbs free energy of the reaction between KCl and the five components of refractory materials in the 600–1200 °C temperature range.
Materials 11 02584 g003
Figure 4. XRD patterns of the products of the reaction between MgO and KCl.
Figure 4. XRD patterns of the products of the reaction between MgO and KCl.
Materials 11 02584 g004
Table 1. Corrosion products and reaction equations of K2CO3 reacting with the five components of refractory materials.
Table 1. Corrosion products and reaction equations of K2CO3 reacting with the five components of refractory materials.
SpeciesTemperature (°C)
600700–1200
Al2O31.3168 mol KAlO2, 0.0569 mol K2Al12O192 mol KAlO2
Equations (3) and (4)Equation (4)
MgO-
Cr2O31 mol K2CrO4
Equation (1)
MgO·Cr2O31 mol K2CrO4, 0.5mol MgO
Equation (2)
MgO·Al2O30.1215 mol KAlO2, 0.0608 mol MgO2 mol KAlO2, 1 mol MgO
Equation (5)Equation (5)
“-”: The amount of corrosion products is less than 10−4 mol.
Table 2. Corrosion products and reaction equations of K2SO4 reacting with the five components of refractory materials.
Table 2. Corrosion products and reaction equations of K2SO4 reacting with the five components of refractory materials.
SpeciesTemperature (°C)
600–900100011001200
Al2O3-0.0009 mol KAl9O140.0062 mol KAl9O14
Equation (7)Equation (7)
MgO-
Cr2O3-0.0002 mol K2CrO40.0015 mol K2CrO40.0076 mol K2CrO4
Equation (6)Equation (6)Equation (6)
MgO·Cr2O3-0.0001 mol K2CrO40.0008 mol K2CrO4
Equation (8)Equation (8)
MgO·Al2O3-
“-”: The amount of corrosion products is less than 10−4 mol.
Table 3. Corrosion products and reaction equations of KCl reacting with the five components of refractory materials.
Table 3. Corrosion products and reaction equations of KCl reacting with the five components of refractory materials.
SpeciesTemperature (°C)
600–900100011001200
Al2O3-0.0002 mol KAl9O140.0004 mol KAl9O140.0009 mol KAl9O14
Equation (8)Equation (8)Equation (8)
MgO-
Cr2O3-0.0003 mol K2CrO40.0005 mol K2CrO40.0006 mol K2CrO4
Equation (10)Equation (10)Equation (10)
MgO·Cr2O3-0.0001 mol K2CrO40.0002 mol K2CrO4
Equation (11)Equation (11)
MgO·Al2O3-
“-”: The amount of corrosion products is less than 10−4 mol.

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MDPI and ACS Style

Zhao, Y.; Cheng, G.; Long, F.; Liu, L.; Dong, C.; Wang, X.; Zhao, J. Analysis and Prediction of Corrosion of Refractory Materials by Potassium during Biomass Combustion-Thermodynamic Study. Materials 2018, 11, 2584. https://doi.org/10.3390/ma11122584

AMA Style

Zhao Y, Cheng G, Long F, Liu L, Dong C, Wang X, Zhao J. Analysis and Prediction of Corrosion of Refractory Materials by Potassium during Biomass Combustion-Thermodynamic Study. Materials. 2018; 11(12):2584. https://doi.org/10.3390/ma11122584

Chicago/Turabian Style

Zhao, Ying, Guishi Cheng, Fei Long, Lu Liu, Changqing Dong, Xiaoqiang Wang, and Jin Zhao. 2018. "Analysis and Prediction of Corrosion of Refractory Materials by Potassium during Biomass Combustion-Thermodynamic Study" Materials 11, no. 12: 2584. https://doi.org/10.3390/ma11122584

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