MSCEJournal of Materials Science and Chemical Engineering2327-6045Scientific Research Publishing10.4236/msce.2018.64005MSCE-83660ArticlesChemistry&Materials Science The Study of the Preparation of Catalysts for Carbonyl Sulfide Hydrolysis under Moderate Temperature YikunXu1ShangguanJu1ZexingWang1YanxiaLiu1Key Laboratory of Coal Science and Technology of Shanxi Province and Ministry of Education, Taiyuan University of Technology, Taiyuan, China12042018060431389, November 20175, April 2018 12, April 2018© Copyright 2014 by authors and Scientific Research Publishing Inc. 2014This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/

Multifunctional composite catalyst for carbonyl sulfide hydrolysis under moderate temperature was prepared by impregnation method. The hydrolysis and deoxidization ability of the prepared catalyst was investigated in a fixed bed reactor. It was found that deoxidization ability of the prepared catalyst was raised by the increase of the content of potassium loading catalyst and reaction temperature. And the concentration of H 2S had no effect on deoxidization while COS improved the deoxidization ratio. And deoxidization rates were nearly scaled up with concentration of H 2. The hydrolysis ability was decreased by the decrease of the surface basicity.

Carbonyl Sulfide Hydrolysis Deoxidization Catalyst Moderate Temperature1. Introduction

In the process of coal coking, through a series of complex physical and chemical reactions, coal was generated into the coke oven gas eventually. Coke oven gas contains a lot of sulfide, hydrogen chloride, hydrogen fluoride and other gases, and trace amount of these compounds can result in the deactivation of the following catalysts and lead to corrosion of the following reaction equipment [1]-[6]. The amount of sulfur in the gas must be decreased to a standardized scope. So the sulfide in coke oven gas must be removed before used. Coke oven gas contains not only hydrogen sulfide (H2S) but also other sulfurous gases including carbonyl sulfide (COS). In comparison to H2S, COS is more difficult to remove due to its low reactivity in many desulfurizers. Therefore, the formation of COS in coke oven gas will reduce the coke oven gas desulfurization efficiency. Many studies of COS removal by sorption, catalytic hydrolysis and hydrogenation conversion have been reported in order to overcome this limitation [7] [8] [9] [10]. An alternative technology has been used for the removal of COS, and this is based on the formation of H2S by hydrolysis: COS + H2O = H2S + CO2.

Liu et al. [11] studied the heterogeneous reaction of COS on metal oxides. The results showed that the activity series for heterogeneous hydrolysis of COS decreased in the following sequence: Al2O3 > CaO > MgO > TiO2 > ZnO > Fe2O3 > SiO2. The specific surface area and surface basicity of these oxides have great effect on the catalytic activity. Shangguan et al. [12] prepared the catalyst containing Al2O3 and K2CO3 at low temperature and an improved desulfurization performance was reported. Loading K2CO3 can increase the basicity of catalyst, which increases the COS hydrolysis ability. However, some desulfurization process must be carried out under intermediate temperatures, and in this temperature, Al2O3 is easy to be sulfated which will decrease the catalytic activity. Liujun et al. [13] thought reduce catalytic activity was due to oxygen existed in gas. The oxygen can make H2S transform into SO42―on the surface of catalyst and this reaction can sulfate the Al2O3, thereby decreasing the basicity of catalysts.

To overcome the pernicious effect of Al2O3 that oxygen brings in, something that can remove oxygen must be introduced into catalyzer. Hydrodeoxygenation has been reported as a feasible way to remove the oxygen. Hydrodeoxygenation refers to the reaction of O2 and H2 generate into H2O to remove oxygen under the influence of deoxidizers. Cu-based deoxidizer has been widely used, but it has low deoxidization accuracy and oxygen capacity. Pd-based deoxidizer has wide operating temperature range and high deoxidization accuracy, but it is expensive and needs strict impurity in the raw material gas. Mn-based deoxidizer cannot be used in sulfur-containing atmosphere while coke oven gas contains a lot of sulfur. Ni-based deoxidizer has very high hydrodeoxygenation catalytic activity, however Ni can react with CO and coke oven gas has some CO. Mo-based deoxidizer has high hydrodeoxygenation catalytic activity, and it still work even in high temperature. In sulfur-containing atmosphere, Mo can generate MoS2 which has better hydrodeoxygenation catalytic activity, so Mo-based deoxidizer can add into middle temperature hydrolysis catalysts to avoid oxygen poisoning.

By considering the deoxidization ability of middle temperature COS hydrolysis catalysts added MoO3 and the change law of the deoxidization ability in different reaction conditions, some researches were investigated in this paper.

2. Experimental2.1. Preparation and Pre-Sulfidation of Catalysts

The COS hydrolysis catalysts doped with MoO3 were prepared using impregnation method. Different mass ration of (NH4)6Mo7O24∙6H2O and K2CO3 were dissolved in some distilled water that accorded with the water absorption of supports. Then the corresponding mass of Al2O3 supports was added into the above solution. The mixture was maintained for 12 h at room temperature. Then put the mixture into the dying oven for 4 h at 120˚C. Finally put them into muffle furnace for calcination activation at 550˚C for 5 h.

2.2. Pre-Sulfidation

Catalyst was heated to 200˚C in a N2 atmosphere, and then H2 and H2S was inlet. H2 concentration was 50% - 60% and H2S concentration was 2000 - 2500 mgS/m3 with N2 balanced.

2.3. Hydrodeoxygenation Tests

Hydrodeoxygenation tests were performed in a fixed-bed micro-reactor. The experimental apparatus consists of gas inlet unit, reaction unit and detecting unit. Gases were controlled by rotameter and then introduced into a vertically quartz tube that was placed in a tube furnace. The inner diameter of the reaction quartz tube was 15 mm. 10 ml of sample was packed in the tube to a height of about 4.5 cm, and then heated to the reaction temperature in a mixed gas flow. The mixed gas contains H2, N2, O2 and H2S or COS. The reaction temperature was range from 200˚C to 300˚C.

2.4. Determination of the Deoxidization Ability

The concentration of O2 in inlet and outlet were determined through CG7900. The changes in the concentration of O2 in inlet and outlet indicate the deoxidization ability of the catalysts.

3. Results and Discussion3.1. The Pre-Sulfidation of Catalysts

At the time of preparing catalysts, Mo was the form of ionic state in the impregnating solution firstly, then transformed into oxidation state when the catalysts were roasting and activating. However, only if molybdenum oxides were transformed into MoS2 can catalysts get more deoxidization ability. The reaction that occurs during the pre-sulfidation process is MoO3 + 2H2S+ H2 = MoS2 + 3H2O + 48.1 kJ.

When the H2S was at a low concentration, the time of pre-sulfidation would be grown. This will take more time for pre-sulfidation process in practical application. When the temperature of pre-sulfidation was too high, H2 would transform Mo oxides into Mo simple substance which could make the active component of hydrodeoxygenation loss. So, the concentration of H2S in sulfidation gas was 2000 - 2500 mgS/m3 and the temperature was 200˚C.

3.2. The Pre-Experiment of Catalysts Hydrodeoxygenation

The change of the ratio of deoxidization for catalyst without Mo was shown in Figure 1 with the increase of time. As shown in Figure 1, the deoxidization ratio

of the catalysts without Mo was nearly zero, and it could be proved that the catalysts without Mo did not have the ability of deoxidization and the oxidation of H2S could not have effect on the determination of deoxidization ratio.

3.3. The Effect of the Molybdenum Content on the Hydrolysis Ability of the Catalysts

The change of the COS hydrolysis conversion for the catalysts was shown in Figure 2 with the increase of time. As shown in Figure 2, A referred to the catalyst without Mo doped, and B referred to the catalyst with 10 wt.% Mo doped, and C was the catalyst that doped with 10 wt.% Mo after pre-sulfurized. The temperature of reactions were 300˚C, and the concentration of H2 was 20%. The hydrolysis ability of the catalyst was decreased with the Mo doped in and this phenomenon was more significant when the catalyst was pre-sulfurized. Because the COS hydrolysis reaction was a base-catalysis, while the Mo doped in made the surface basicity decrease and decreased the hydrolysis ability eventually. And the pre-sulfidation made the surface basicity decrease further. It might be that after the pre-sulfidation the S2-occupied lots of surface space and made the COS difficult to combine with surface basic sites. Though the hydrolysis ability decreased with addition of Mo, it can make the catalyst have the ability of deoxidization to avoid the pernicious effect of Al2O3 that oxygen brought in.

3.4. The Effect of Temperature and the Potassium Content on the Deoxidization Ability of the Catalysts

Influences of temperature and the content of potassium on the ratio of deoxidization of catalyst were shown in Table 1.

As shown in the Table 1, it can be concluded that the deoxidization ability raised with the increase of reaction temperature and the potassium content. From the thermodynamics, the hydrodeoxygenation reaction is an exothermic

Influences of different Temperature and different potassium content on the ratio of deoxidization of catalyst
Content of potassium (%)Ratio of deoxidization in different temperature (%)
200˚C250˚C300˚C
51.122.583.14
101.374.736.83
159.6730.3950.41

process, so deoxidization ability should be decreased with the increase of the reaction temperature. However, the actual deoxidization ratio showed the opposite tendency, this may be because that the hydrodeoxygenation reaction is away from the chemical equilibrium, catalyst improves the chemical reaction rate and the reaction rate increase with the temperature raising. As for potassium content, the H+ in surface hydroxyl was replaced by K+ with the potassium added in which could reduce the phase change of Al2O3 and accelerate electron transfer of activated oxygen and activated hydrogen. And K+ not only could prompt Mo4+ into stable Mo5+ but also was the active center of oxidation-reduction reaction.

3.5. The Effect of Sulfur-Containing Atmosphere the Deoxidization Ability of the Catalysts

The change of the ratio of deoxidization for catalyst in different sulfur containing atmosphere was shown in Figure 3 with the increase of time. As shown in Figure 3, the 80, 200, 700, 1100 referred to the concentration of H2S, and that were 80 mgS/m3, 200 mgS/m3, 700 mgS/m3, 1100 mgS/m3. And the concentration of COS was 700 mgS/m3. The temperature of reactions were 300˚C, and the concentration of H2 was 20%. The ratio of deoxidization did not significantly changed with the increased of the concentration of H2S, however in COS

atmosphere the ratio of deoxidization was raised a lot. That may be in COS atmosphere, the COS hydrolysis reaction can raise the concentration of surface O 2 − in Al2O3 which is beneficial to the absorption of H2 and finally increase the ratio of deoxidization. In COS atmosphere the conversion of COS and H2S may make the deoxidization unstable.

3.6. The Effect of the Concentration of H<sub>2 </sub>on the Deoxidization Ability of the Catalysts

The change of the ratio of deoxidization for catalyst in different concentration of H2 was shown in Figure 4 with the increase of time. As shown in Figure 4, the ratio of deoxidization of catalyst were raised with the increase of the concentration of H2. The ratio of deoxidization were nearly scaled up with concentration of H2, so it can be concluded that the controlling process of hydrodeoxygenation reaction was connected with H2 and that process might be a second order reaction.

4. Conclusion

At the process of catalyst deoxidization, the potassium can improve the deoxidization ability of the catalysts, and the improvement raised with the increase of potassium contents while at the process of hydrolysis the surface basicity decrease make the hydrolysis ability decrease. Catalyst improves the deoxidization rate and the deoxidization rate increase with the temperature raising. In the H2S containing atmosphere the ratio of deoxidization did not change with the change of the concentration of H2S, however in the COS atmosphere the ratio of deoxidization raised a lot. The ratio of deoxidization scaled up with the increased of the concentration of H2 and that may be a second order reaction.

Acknowledgements

This work was supported by the National Natural Science Foundation of China (No. 20976116) and the Major Project of Science and Technology of Shanxi Province in 2016 (MJH2016-03).

Cite this paper

Xu, Y.K., Ju, S.G., Wang, Z.X. and Liu, Y.X. (2018) The Study of the Preparation of Catalysts for Carbonyl Sulfide Hydrolysis under Moderate Temperature. Journal of Materials Science and Chemical Engineering, 6, 31-38. https://doi.org/10.4236/msce.2018.64005

ReferencesWang, J., Liu, L., Han, L., Hu, Y., Chang, L. and Bao, W. (2013) Alumina-Supported Manganese Oxide Sorbent Prepared by Sub-Critical Water Impregnation for Hot Coal Gas Desulfurization. Fuel Processing Technology, 110, 235-241. https://doi.org/10.1016/j.fuproc.2012.12.020Cheah, S., Carpenter, D.L. and Magrinibair, K.A. (2009) Review of Mid- to High-Temperature Sulfur Sorbents for Desulfurization of Biomass- and Coal-Derived Syngas. Journal of Southwest Petroleum Institute, 23, 5291-5307. https://doi.org/10.1021/ef900714qMathieu, Y., Tzanis, L., Soulard, M., Patarin, J., Vierling, M. and Molière, M. (2013) Adsorption of SOx by Oxide Materials: A Review. Fuel Processing Technology, 114, 81-100. https://doi.org/10.1016/j.fuproc.2013.03.019Yang, L., Dong, Y., Zhang, Y. and Xie, K. (2006) Present Situation and Development Prospect of Coke Oven Gas Utilization in China. Energy and Conservation, 1, 1-4.Whelan, M.E., Min, D.H. and Rhew, R.C. (2013) Salt Marsh Vegetation as a Carbonyl Sulfide (COS) Source to the Atmosphere. Atmospheric Environment, 73, 131-137. https://doi.org/10.1016/j.atmosenv.2013.02.048Ahmad, N., Husain, M.I., Kumar, R., et al. (2012) Comparative Kinetics of Corrosion Rate on Mild Steel in Various Citrus Juices. Ijsat Com, 2, 2221-8386.Jia, Z., Duan, X., Qin, P., et al. (2017) Disordered Atomic Packing Structure of Metallic Glass: Toward Ultrafast Hydroxyl Radicals Production Rate and Strong Electron Transfer Ability in Catalytic Performance. Advanced Functional Materials, 1702258. https://doi.org/10.1002/adfm.201702258Liang, S.X., Jia, Z., Zhang, W.C., et al. (2017) Rapid Malachite Green Degradation Using Fe73.5Si13.5B9Cu1Nb3, Metallic Glass for Activation of Persulfate under UV-Vis Light. Materials & Design, 119, 244-253. https://doi.org/10.1016/j.matdes.2017.01.039Jia, Z., Kang, J., Zhang, W.C., et al. (2017) Surface Aging Behaviour of Fe-Based Amorphous Alloys as Catalysts during Heterogeneous Photo Fenton-Like Process for Water Treatment. Applied Catalysis B Environmental, 204, 537-547. https://doi.org/10.1016/j.apcatb.2016.12.001Jia, Z., Zhang, W.C., Wang, W.M., et al. (2016) Amorphous Fe78Si9B13 Alloy: A Rapid and Reusable Photo-Enhanced Fenton-Like Catalyst in Degradation of Cibacron Brilliant Red 3B-A Dye under UV-Vis Light. Applied Catalysis B Environmental, 192, 46-56. https://doi.org/10.1016/j.apcatb.2016.03.048Liu, Y. and He, H. (2009) Experimental and Theoretical Study of Hydrogen Thiocarbonate for Heterogeneous Reaction of Carbonyl Sulfide on Magnesium Oxide. Journal of Physical Chemistry A, 113, 3387-3394. https://doi.org/10.1021/jp809887cJu, S.G., Zhao, Y.S., Fan, H.L., Liang, L.T., Shen, F. and Miao, M.Q. (2013) Desul-furization Behavior of Zinc Oxide Based Sorbent Modified by the Combination of Al2O3 and K2CO3. Fuel, 108, 80-84. https://doi.org/10.1016/j.fuel.2011.04.011Liu, J., Liu, Y., Li, X., Yu, Y. and Hong, H. (2007) Oxygen Poisoning Mechanism of Catalytic Hydrolysis of OCS over Al2O3 at Room Temperature. Acta Physico-Chimica Sinica, 23, 997-1002. https://doi.org/10.1016/S1872-1508(07)60054-0