工程科学学报
工程科學學報
공정과학학보
Journal of University of Science and Technology Beijing
2015年
8期
1049-1056
,共8页
李哲%汪莉%贠丽%王振南%李梦霞%李鑫
李哲%汪莉%贠麗%王振南%李夢霞%李鑫
리철%왕리%원려%왕진남%리몽하%리흠
氧化物%催化剂%选择性催化还原%一氧化氮%活性
氧化物%催化劑%選擇性催化還原%一氧化氮%活性
양화물%최화제%선택성최화환원%일양화담%활성
oxides%catalysts%selective catalytic reduction%nitrogen oxide%activity
采用溶胶凝胶法制备TiO2-ZrO2载体,然后采用柠檬酸溶液浸渍法制备Cr-MnOx/TiO2-ZrO2复合催化剂.通过X射线衍射、比表面积测试( BET)、扫描电镜、X射线光电子能谱等测试方法对催化剂的物化性能进行表征分析,并进行NH3选择性催化还原NO实验,考察催化剂在低温下的活性及抗硫抗水性能. Cr元素介入到MnOx 中,形成了新型的CrMn1.5 O4活性物相,其中的Mn元素多以Mn3+和Mn4+存在.高价态的Cr5+使Mn元素由Mn3+向高氧化态的Mn4+转化,有利于低温选择性催化还原反应的进行.鉴于Cr元素第一电离能和电负性均低于Mn元素,能优先于Mn与SO2-4和SO2-3结合,保护MnOx 不被硫酸化,从而提高Cr-MnOx/TiO2-ZrO2催化剂的抗毒性能.制备的五种不同Cr/(Cr+Mn)摩尔比的催化剂中,Cr(0.4)-MnOx/TiO2-ZrO2的性能最优,其颗粒分散均匀,具有较大比表面积,在180℃时脱硝效率能够达到95.8%,同时通入5% H2 O和10-4 SO2,脱硝效率缓慢下降,反应8 h后,下降到73%,并保持稳定.
採用溶膠凝膠法製備TiO2-ZrO2載體,然後採用檸檬痠溶液浸漬法製備Cr-MnOx/TiO2-ZrO2複閤催化劑.通過X射線衍射、比錶麵積測試( BET)、掃描電鏡、X射線光電子能譜等測試方法對催化劑的物化性能進行錶徵分析,併進行NH3選擇性催化還原NO實驗,攷察催化劑在低溫下的活性及抗硫抗水性能. Cr元素介入到MnOx 中,形成瞭新型的CrMn1.5 O4活性物相,其中的Mn元素多以Mn3+和Mn4+存在.高價態的Cr5+使Mn元素由Mn3+嚮高氧化態的Mn4+轉化,有利于低溫選擇性催化還原反應的進行.鑒于Cr元素第一電離能和電負性均低于Mn元素,能優先于Mn與SO2-4和SO2-3結閤,保護MnOx 不被硫痠化,從而提高Cr-MnOx/TiO2-ZrO2催化劑的抗毒性能.製備的五種不同Cr/(Cr+Mn)摩爾比的催化劑中,Cr(0.4)-MnOx/TiO2-ZrO2的性能最優,其顆粒分散均勻,具有較大比錶麵積,在180℃時脫硝效率能夠達到95.8%,同時通入5% H2 O和10-4 SO2,脫硝效率緩慢下降,反應8 h後,下降到73%,併保持穩定.
채용용효응효법제비TiO2-ZrO2재체,연후채용저몽산용액침지법제비Cr-MnOx/TiO2-ZrO2복합최화제.통과X사선연사、비표면적측시( BET)、소묘전경、X사선광전자능보등측시방법대최화제적물화성능진행표정분석,병진행NH3선택성최화환원NO실험,고찰최화제재저온하적활성급항류항수성능. Cr원소개입도MnOx 중,형성료신형적CrMn1.5 O4활성물상,기중적Mn원소다이Mn3+화Mn4+존재.고개태적Cr5+사Mn원소유Mn3+향고양화태적Mn4+전화,유리우저온선택성최화환원반응적진행.감우Cr원소제일전리능화전부성균저우Mn원소,능우선우Mn여SO2-4화SO2-3결합,보호MnOx 불피류산화,종이제고Cr-MnOx/TiO2-ZrO2최화제적항독성능.제비적오충불동Cr/(Cr+Mn)마이비적최화제중,Cr(0.4)-MnOx/TiO2-ZrO2적성능최우,기과립분산균균,구유교대비표면적,재180℃시탈초효솔능구체도95.8%,동시통입5% H2 O화10-4 SO2,탈초효솔완만하강,반응8 h후,하강도73%,병보지은정.
Using a sol-gel prepared TiO2- ZrO2 carrier, Cr- MnOx/TiO2- ZrO2 composite catalysts were synthesized by a critic acid solution impregnation method. The physical and chemical properties of the catalysts were characterized by X-ray diffraction, specific surface area determination ( BET) , scanning electron microscopy and X-ray photoelectron spectroscopy. Meanwhile, the low-temperature catalytic activity and the sulfur and water resistance were evaluated with selective catalytic reduction ( SCR) of NO by NH3. The introduction of Cr element to MnOx yields a new CrMn1.5O4 active phase, in which Mn primarily exists as Mn3+ and Mn4+. The Cr5+ valence state facilitates the transformation of Mn3+ to high oxidation state Mn4+, which is beneficial to the low temperature SCR reaction. Because of lower first ionization energy and electronegativity, Cr preferentially reacts with SO2-4 and SO2-3 than Mn, thus protecting MnOx not to be sulphatized and resulting in the enhanced antitoxic performance of Cr-MnOx/TiO2-ZrO2 . Among the prepared five catalysts with different molar ratios of Cr/(Cr+Mn), Cr(0. 4)- MnOx/TiO2- ZrO2 demonstrates the best performance owing to the largest surface area and the best particle dispersion, and a 95. 8% denitrification efficiency can be achieved at 180℃. When 5% H2 O and 10 -4 SO2 are simultaneously added, the denitrification efficiency decreases slowly and stabilizes at 73% after 8 h reaction.