功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2015年
10期
10090-10094,10099
,共6页
贡湘君%叶飞%刘荣%管昊%季凌晨%杨铭
貢湘君%葉飛%劉榮%管昊%季凌晨%楊銘
공상군%협비%류영%관호%계릉신%양명
四方相氧化锆%MnOx-CeO2/t-ZrO2 催化剂%脱硝活性
四方相氧化鋯%MnOx-CeO2/t-ZrO2 催化劑%脫硝活性
사방상양화고%MnOx-CeO2/t-ZrO2 최화제%탈초활성
tetragonal-phase zirconium%MnOx-CeO2/t-ZrO2 catalysts%denitration activity
以纳米 t-ZrO2为载体,用浸渍法制备出MnOx-CeO2/t-ZrO2催化剂,考察了活性组分负载量、反应温度对催化剂 NH3-SCR 脱硝活性的影响,脱硝活性测试结果显示,在低温脱硝温度范围,催化剂脱硝效率随反应温度和活性组分负载量的增加而增加.反应温度为100℃时,2.5%MnOx-CeO2/t-ZrO2脱硝效率为68.1%,15%MnOx-CeO2/t-ZrO2脱硝效率达97.4%.XRD、BET、TPR 等表征测试结果表明,催化剂表面具有良好的氧化还原能力,表面织构对 NH3-SCR 脱硝反应有利;NH3-TPD 测试显示,MnOx-CeO2/t-ZrO2催化剂表面NH3主要吸附在 Lewis 酸性位成配位态NH3,与气态NO 反应生产中间产物NH2 NO,最后分解为N2和 H2O.
以納米 t-ZrO2為載體,用浸漬法製備齣MnOx-CeO2/t-ZrO2催化劑,攷察瞭活性組分負載量、反應溫度對催化劑 NH3-SCR 脫硝活性的影響,脫硝活性測試結果顯示,在低溫脫硝溫度範圍,催化劑脫硝效率隨反應溫度和活性組分負載量的增加而增加.反應溫度為100℃時,2.5%MnOx-CeO2/t-ZrO2脫硝效率為68.1%,15%MnOx-CeO2/t-ZrO2脫硝效率達97.4%.XRD、BET、TPR 等錶徵測試結果錶明,催化劑錶麵具有良好的氧化還原能力,錶麵織構對 NH3-SCR 脫硝反應有利;NH3-TPD 測試顯示,MnOx-CeO2/t-ZrO2催化劑錶麵NH3主要吸附在 Lewis 痠性位成配位態NH3,與氣態NO 反應生產中間產物NH2 NO,最後分解為N2和 H2O.
이납미 t-ZrO2위재체,용침지법제비출MnOx-CeO2/t-ZrO2최화제,고찰료활성조분부재량、반응온도대최화제 NH3-SCR 탈초활성적영향,탈초활성측시결과현시,재저온탈초온도범위,최화제탈초효솔수반응온도화활성조분부재량적증가이증가.반응온도위100℃시,2.5%MnOx-CeO2/t-ZrO2탈초효솔위68.1%,15%MnOx-CeO2/t-ZrO2탈초효솔체97.4%.XRD、BET、TPR 등표정측시결과표명,최화제표면구유량호적양화환원능력,표면직구대 NH3-SCR 탈초반응유리;NH3-TPD 측시현시,MnOx-CeO2/t-ZrO2최화제표면NH3주요흡부재 Lewis 산성위성배위태NH3,여기태NO 반응생산중간산물NH2 NO,최후분해위N2화 H2O.
The MnOx-CeO2/t-ZrO2 catalyst was prepared by impregnation with nano t-ZrO2 as the supporter. The influence of active component and reaction temperature on denitration performance of catalyst was investi-gated.The results showed that denitration efficiency improved as active component increased and reaction tem-perature rose.The denitration efficiency of 2.5% MnOx-CeO2/t-ZrO2 at 100 ℃ was 68.1% while 15% MnOx-CeO2/t-ZrO2 was 97.4%.The results of XRD,BET and H2-TPR showed that surface structure of loaded cata-lyst was good for oxidation-reduction and denigration.NH3-TPD test demonstrated that NH3 was mainly ad-sorbed at Lewis acid sites on the surface of catalysts and became coordination NH3 .Intermediate product NH2 NO generated from reactions between coordination NH3 and NO which finally changed into N2 and H2 O.