化工学报
化工學報
화공학보
JOURNAL OF CHEMICAL INDUSY AND ENGINEERING (CHINA)
2014年
12期
4805-4813
,共9页
王栋%张信莉%路春美%韩奎华%彭建升%徐丽婷
王棟%張信莉%路春美%韓奎華%彭建升%徐麗婷
왕동%장신리%로춘미%한규화%팽건승%서려정
γ-Fe2O3%催化剂%微波%热解%选择催化还原%脱硝
γ-Fe2O3%催化劑%微波%熱解%選擇催化還原%脫硝
γ-Fe2O3%최화제%미파%열해%선택최화환원%탈초
γ-Fe2O3%catalyst%microwave%pyrolysis%SCR%DeNOx
以 FeSO4·7H2O[Fe(NO3)3·9H2O]为铁源,采用新型微波热解法制备γ-Fe2O3[α-Fe2O3]催化剂样品,通过XRD、N2等温吸附-脱附、压汞法等实验手段对催化剂样品晶相、微观孔结构等进行表征;考察两种催化剂样品的 NH3-SCR 脱硝性能,通过归一化处理得到两种催化剂在不同温度下的本征脱硝反应速率,同时对比研究了γ-Fe2O3与钒系催化剂的脱硝活性;研究氨氮比、氧浓度等运行参数对γ-Fe2O3催化剂NH3-SCR脱硝性能的影响规律,并对其抗硫抗水性能进行考察。结果表明:采用新型微波热解法可得到纯度较高的γ-Fe2O3催化剂,其介孔分布合理且大孔数量丰富;同时γ-Fe2O3催化剂表现出优于α-Fe2O3催化剂的脱硝性能,400℃时最大 NOx转化率达到96%,300、325、350℃下单位面积脱硝速率达到α-Fe2O3催化剂的3倍左右;γ-Fe2O3催化剂具备优良的抗硫抗水性能,其最佳氨氮比为1、最佳氧体积分数为3.5%。
以 FeSO4·7H2O[Fe(NO3)3·9H2O]為鐵源,採用新型微波熱解法製備γ-Fe2O3[α-Fe2O3]催化劑樣品,通過XRD、N2等溫吸附-脫附、壓汞法等實驗手段對催化劑樣品晶相、微觀孔結構等進行錶徵;攷察兩種催化劑樣品的 NH3-SCR 脫硝性能,通過歸一化處理得到兩種催化劑在不同溫度下的本徵脫硝反應速率,同時對比研究瞭γ-Fe2O3與釩繫催化劑的脫硝活性;研究氨氮比、氧濃度等運行參數對γ-Fe2O3催化劑NH3-SCR脫硝性能的影響規律,併對其抗硫抗水性能進行攷察。結果錶明:採用新型微波熱解法可得到純度較高的γ-Fe2O3催化劑,其介孔分佈閤理且大孔數量豐富;同時γ-Fe2O3催化劑錶現齣優于α-Fe2O3催化劑的脫硝性能,400℃時最大 NOx轉化率達到96%,300、325、350℃下單位麵積脫硝速率達到α-Fe2O3催化劑的3倍左右;γ-Fe2O3催化劑具備優良的抗硫抗水性能,其最佳氨氮比為1、最佳氧體積分數為3.5%。
이 FeSO4·7H2O[Fe(NO3)3·9H2O]위철원,채용신형미파열해법제비γ-Fe2O3[α-Fe2O3]최화제양품,통과XRD、N2등온흡부-탈부、압홍법등실험수단대최화제양품정상、미관공결구등진행표정;고찰량충최화제양품적 NH3-SCR 탈초성능,통과귀일화처리득도량충최화제재불동온도하적본정탈초반응속솔,동시대비연구료γ-Fe2O3여범계최화제적탈초활성;연구안담비、양농도등운행삼수대γ-Fe2O3최화제NH3-SCR탈초성능적영향규률,병대기항류항수성능진행고찰。결과표명:채용신형미파열해법가득도순도교고적γ-Fe2O3최화제,기개공분포합리차대공수량봉부;동시γ-Fe2O3최화제표현출우우α-Fe2O3최화제적탈초성능,400℃시최대 NOx전화솔체도96%,300、325、350℃하단위면적탈초속솔체도α-Fe2O3최화제적3배좌우;γ-Fe2O3최화제구비우량적항류항수성능,기최가안담비위1、최가양체적분수위3.5%。
γ-Fe2O3 andα-Fe2O3 catalysts were prepared respectivelyvia a novel microwave pyrolysis method using FeSO4·7H2O and Fe(NO3)3·9H2O as ferrous source. Crystalline phase and microstructure of catalysts were characterized by X-ray diffraction(XRD), mercury intrusion porosimetry(MIP), N2 adsorption-desorption and NH3-SCR activity of different catalysts were investigated. SCR reaction rates over the catalysts at different temperatures were obtained by unitary processing, and SCR activities overγ-Fe2O3 and vanadium-based catalysts were compared. The effects of O2 concentration, molar ratio of NH3/NO, SO2, and H2O on SCR activity ofγ-Fe2O3 catalyst were also studied. Pureγ-Fe2O3 catalyst could be obtainedvia this novel microwave pyrolysis method, and showed higher crystallinity thanα-Fe2O3 catalyst.γ-Fe2O3 catalyst had broader pore size distribution as well as appropriate ratios of mesopores and macropores. Meanwhile,γ-Fe2O3 catalyst exhibited better SCR activity thanα-Fe2O3 catalyst. The highest NOx conversion ofγ-Fe2O3 catalyst was up to 96% at 400℃ and SCR reaction rates normalized by surface area were three times higher than that ofα-Fe2O3 catalyst at 300, 325 and 350℃, respectively. The optimum molar ratio of NH3/NO and O2 concentration for selective catalytic reduction overγ-Fe2O3 catalyst were recommended to be 1 and 3.5% (vol), respectively.