含铈钒基SCR催化剂脱硝性能及SO2失活机理研究

Activity and SO2 deactivation mechanism of vanadium series catalyst containing cerium

  • 摘要: 掺杂Ce到V2O5-WO3/TiO2催化剂中,并研究其NH3-SCR脱硝性能及SO2失活机理。结果表明,V1W5Ce6Ti表现出更好的脱硝活性。采用XRD、BET、FT-IR、TG-DSC、XPS等手段表征分析Ce对催化剂性能的影响,并提出V1W5Ce6Ti硫失活机理。结果表明,Ce、V、W都能在催化剂中很好的分散,当Ce的掺杂量达到8%时,有明显的CeO2特征峰出现。在250℃时,V1W5Ti(U)表面会有NH4HSO4和(NH42SO4生成。掺杂Ce后,V1W5Ce6Ti催化剂的Brønste酸位和表面化学吸附氧都增加。Ce与烟气中的SO2和H2O结合生成硫酸铈盐,从而抑制硫酸铵盐的生成。同时也阻断了Ce3+与Ce4+氧化还原循环,破坏V-O-Ce结构,造成催化剂活性下降。

     

    Abstract: The promotion effect of Ce modification on V2O5-WO3/TiO2 for the selective catalytic reduction (SCR) of NOx with NH3 and the SO2 deactivation mechanism were investigated. Compared with V1W5Ti catalyst, the advantage of V1W5Ce6Ti catalyst shows a good catalytic activity. These catalysts were investigated by means of XRD, BET, FT-IR, TG-DSC and XPS. The results demonstrate that the active components of V and W are well-dispersed, while a small cluster of cubic CeO2 appears over the V1W5Ce8Ti catalyst. The sulfation of V1W5Ti under reactive conditions can generate NH4HSO4 and (NH4)2SO4 at 250℃. The Ce additive to V1W5Ti could provide stronger Brønsted acid sites and more chemisorbed oxygen. The deposited ammonium sulfate on V1W5Ce6Ti catalyst is much smaller than that on V1W5Ti because the cerium sulfates species on the surface of V1W5Ce6Ti is formed and the deposition of ammonium sulfate is inhibited, which can disrupt the redox cycle between Ce3+ and Ce4+ and break the V-O-Ce structure, causing the deactivation of V1W5Ce6Ti catalyst.

     

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