燃料化学学报
燃料化學學報
연료화학학보
Journal of Fuel Chemistry and Technology
2015年
9期
1106-1112
,共7页
王虹%李滨%卢学斌%李翠清%丁福臣%宋永吉
王虹%李濱%盧學斌%李翠清%丁福臣%宋永吉
왕홍%리빈%로학빈%리취청%정복신%송영길
氮氧化物%甲烷%选择性催化还原%钴氧化物%丝光沸石
氮氧化物%甲烷%選擇性催化還原%鈷氧化物%絲光沸石
담양화물%갑완%선택성최화환원%고양화물%사광비석
nitric oxide%methane%selective catalytic reduction%cobalt oxide%mordenite
采用浸渍法制备了一系列用于甲烷选择催化还原( CH4-SCR)氮氧化物的 Co/MOR 催化剂。采用 XRD、BET、TG-MS、H2-TPR、NH3-TPD和NO-TPD等手段对催化剂进行表征,并对其在甲烷选择催化还原氮氧化物反应中的活性进行评价。结果表明,钴物种以Co3 O4尖晶石形态存在于Co/MOR催化剂中;与MOR载体相比,引入钴物种后,催化剂的酸性、氧化还原能力和对NO的吸脱附能力均发生了变化。在甲烷选择催化还原氮氧化物反应中,Co/MOR的催化活性与其氧化还原性能和对NO的吸脱附性能直接相关;其中, Co 负载量为10%的 Co (10)/MOR 催化剂的 CH4-SCR 脱硝活性最好,在330℃下NO的转化率达54.2%。
採用浸漬法製備瞭一繫列用于甲烷選擇催化還原( CH4-SCR)氮氧化物的 Co/MOR 催化劑。採用 XRD、BET、TG-MS、H2-TPR、NH3-TPD和NO-TPD等手段對催化劑進行錶徵,併對其在甲烷選擇催化還原氮氧化物反應中的活性進行評價。結果錶明,鈷物種以Co3 O4尖晶石形態存在于Co/MOR催化劑中;與MOR載體相比,引入鈷物種後,催化劑的痠性、氧化還原能力和對NO的吸脫附能力均髮生瞭變化。在甲烷選擇催化還原氮氧化物反應中,Co/MOR的催化活性與其氧化還原性能和對NO的吸脫附性能直接相關;其中, Co 負載量為10%的 Co (10)/MOR 催化劑的 CH4-SCR 脫硝活性最好,在330℃下NO的轉化率達54.2%。
채용침지법제비료일계렬용우갑완선택최화환원( CH4-SCR)담양화물적 Co/MOR 최화제。채용 XRD、BET、TG-MS、H2-TPR、NH3-TPD화NO-TPD등수단대최화제진행표정,병대기재갑완선택최화환원담양화물반응중적활성진행평개。결과표명,고물충이Co3 O4첨정석형태존재우Co/MOR최화제중;여MOR재체상비,인입고물충후,최화제적산성、양화환원능력화대NO적흡탈부능력균발생료변화。재갑완선택최화환원담양화물반응중,Co/MOR적최화활성여기양화환원성능화대NO적흡탈부성능직접상관;기중, Co 부재량위10%적 Co (10)/MOR 최화제적 CH4-SCR 탈초활성최호,재330℃하NO적전화솔체54.2%。
A series of Co/MOR catalysts were prepared by impregnation method and used in the selective catalytic reduction of nitric oxide with methane ( CH4-SCR) . These catalysts were characterized by XRD, BET, TG-MS, H2-TPR, NH3-TPD and NO-TPD; their performance in the CH4-SCR of NO was investigated. The results showed that cobalt species exist as Co3 O4 spinal in the Co/MOR catalysts;the acidity and redox and NO absorption/desorption ability of the Co/MOR catalysts are changed after the incorporation of cobalt in MOR zeolite, in comparison with pure MOR zeolite. The catalytic performance of Co/MOR is closely related to its redox and NO adsorption/desorption ability, which are dependent on the cobalt loading. The Co ( 10 )/MOR catalyst with a cobalt loading of 10% exhibits high activity in the CH4-SCR of NO; over it the conversion of nitric oxide reaches 54 . 2% at 330℃.