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Frontiers of Chemical Science and Engineering

ISSN 2095-0179

ISSN 2095-0187(Online)

CN 11-5981/TQ

Postal Subscription Code 80-969

2018 Impact Factor: 2.809

Front Chem Eng Chin    2010, Vol. 4 Issue (4) : 429-434    https://doi.org/10.1007/s11705-010-0504-y
RESEARCH ARTICLE
Desulfurization performance of iron-manganese-based sorbent for hot coal gas
Xiurong REN, Weiren BAO, Fan LI, Liping CHANG(), Kechang XIE
Key Laboratory of Coal Science and Technology, Ministry of Education and Shanxi Province, Taiyuan University of Technology, Taiyuan 030024, China
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Abstract

A series of iron-manganese-based sorbents were prepared by co-precipitation and physical mixing method, and used for H2S removal from hot coal gas. The sulfidation tests were carried out in a fixed-bed reactor with space velocity of 2000 h-1(STP). The results show that the suitable addition of manganese oxide in iron-based sorbent can decrease H2S and COS concentration in exit before breakthrough due to its simultaneous reaction capability with H2S and COS. Fe3O4 and MnO are the initial active components in iron-manganese-based sorbent, and FeO and Fe are active components formed by reduction during sulfidation. The crystal phases of iron affect obviously their desulfurization capacity. The reducibility of sorbent changes with the content of MnO in sorbent. S7F3M and S3F7M have bigger sulfur capacities (32.68 and 32.30 gS/100 g total active component), while S5F5M has smaller sulfur capacity (21.92 gS/100 g total active component). S7F3M sorbent has stable sulfidation performance in three sulfidation-regeneration cycles and no apparent structure degradation. The sulfidation performance of iron- manganese-based sorbent is also related with its specific surface area and pore volume.

Keywords iron-manganese-based sorbent      sulfidation performance      regeneration      hot coal gas     
Corresponding Author(s): CHANG Liping,Email:lpchang@tyut.edu.cn   
Issue Date: 05 December 2010
 Cite this article:   
Xiurong REN,Weiren BAO,Fan LI, et al. Desulfurization performance of iron-manganese-based sorbent for hot coal gas[J]. Front Chem Eng Chin, 2010, 4(4): 429-434.
 URL:  
https://academic.hep.com.cn/fcse/EN/10.1007/s11705-010-0504-y
https://academic.hep.com.cn/fcse/EN/Y2010/V4/I4/429
Fig.1  Schematic diagram of experimental setup
gas compositionH2a)CO a)CO2a)N2a)H2S b) /ppmO2b)H2O b)
sulfidation39.632.719.5balance25005.6
regeneration88210
Tab.1  Gas composition for sulfidation and regeneration (vol-%)
Fig.2  Breakthrough curves of sorbents with different Fe/Mn atomic ratios at 500°C
sorbentsbulk density /(g·mL-1)specific surface area /(m2·g-1)specific pore volume /(cm3·g-1)crystal phases a)
SF0.9154.930.016Fe3O4, SiO2
S7F3M1.0035.100.032Fe3O4, SiO2, MnO
S5F5M1.0012.500.012Fe3O4, MnO, SiO2
S3F7M1.0353.330.017Fe3O4, MnO, SiO2
SM1.0392.780.009MnO, SiO2
Tab.2  Physical parameter of fresh and pre-reduced sorbents
Fig.3  a SiO; e MnO; g MnS; h FeO; i FeS or FeS; j FeC
XRD patterns of sulfided samples
Fig.4  Breakthrough curves of S7F3M at different temperature
Fig.5  H-TPR patterns of sorbents SF, SM and S7F3M
Fig.6  a SiO; g MnS; h FeO; i FeS or FeS; j FeC
XRD patterns of sulfided S7F3M at different temperatures
Fig.7  Sulfidation breakthrough curves of S7F3M in three cycles
sorbentfresh1st sulfidation1st regeneration2nd sulfidation2nd regeneration3rd sulfidation3rd regeneration
compressive strength /(N·cm-1)122.80128.29139.65130.42149.61135.82140.52
Tab.3  Compressive strength of S7F3M after every sulfidation-regeneration cycles
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