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作 者:宋淑美[1] 马涛[1] 姚远[1] 王睿[1] 赵海霞[1]
机构地区:[1]山东大学环境科学与工程学院,山东济南250100
出 处:《燃料化学学报》2009年第1期87-92,共6页Journal of Fuel Chemistry and Technology
基 金:国家自然科学基金(20576064;20776080);教育部"新世纪优秀人才支持计划"(NCET-05-0584);山东省"优秀中青年科学家科研奖励基金"(2006BS08020)
摘 要:采用乙醚萃取法、浸渍法制备了具有吸附-分解NOx功能的多酸催化新体系,并对其进行了IR、XRD、TEM表征,在固定床催化反应器中考察了体系对NOx的吸附与分解性能。结果表明,钨系杂多酸优于钼系,H3PMo12-xWxO40(x=1、3、6、12)随着取代钼的钨原子数目增多,对NOx的吸附能力增强;二氧化钛、碳纳米管均为磷钨酸(HPW)的优良载体,后者对体系有明显的增效作用;TiO2经500℃煅烧后,以磷钨酸水溶液为浸渍剂,HPW负载量为20%时,制得的HPW/TiO2体系的脱硝性能最佳,对NOx的吸附率可达62.8%;混酸(VHNO3∶VH2SO4=1∶3)能在碳纳米管上引入含氧基团使其在水中的分散性能增强,以水为浸渍溶剂、混酸改性后的碳纳米管为载体制得的HPW/CNT催化体系优于乙醇为浸渍溶剂制备的该催化体系,当HPW负载量为70%时,前者对NOx的吸附率可达73.5%。通过GC-MS检测确认了吸附质催化分解为N2的有效性。Several catalysts of heteropoly compounds (HPCs) with the performance of NOx adsorptiondecomposition were prepared by means of ethanol-extraction and impregnation. The catalysts were characterized by IR, XRD and TEM and evaluated in a fixed-bed reactor. The results showed that tungsten containing HPCs were superior to molybdenum containing HPCs for NOx adsorption ; with the increase of the number of molybdenum atoms substituted by tungsten in H3 PMo12-xWxO40 (x = 1 ,3,6,12) , its NOx adsorption efficiency increased. Titania and carbon nanotube (CNT) were good supports for H3 PW12 040 ( HPW ) ; CNT performed better than titania on the adsorption of NOx. When TiO2 was calcinated at 500 ℃ and the HPW loading was 20% , the NOx adsorption efficiency of HPW/TiO2 reached 62.8%. Mixed HNOa/H2SOg with a volume ratio of 1:3 could produce functional groups such as COO- and C = O on the surface of CNT, which could enhance the dispersion of CNT in the aqueous solution. HPW/CNT catalyst prepared with HNO3/H2SO4-modified CNT as support and using water as impregnation solvent was superior to that using ethanol as impregnation solvent; with the HPW loading of 70%, the adsorption efficiency of NOx by HPW/CNT reached 73.5%. The process effectiveness for NOx decomposition into N2 was confirmed by GC-MS analysis.
分 类 号:X511[环境科学与工程—环境工程]
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