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生物脱硫固定床反应器中的Fe^(2+)氧化动力学 被引量:1

Kinetics of oxidation of Fe^(2+) in fixed-bed bioreactor for biodesulfurization
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摘要 生物脱硫技术中,Fe2+氧化速率是制约整个脱硫工艺效率的关键因素。以两种尺寸的木屑作为固定化载体,分析了反应器中Fe2+氧化动力学。根据所推导的Fe2+氧化动力学方程,对Fe2+浓度随时间衰减的实验值进行非线性拟合分析,确定了反应器分别采用两种载体在最优通气速率下的Fe2+氧化反应级数,并分析了木屑载体(b)的氧化动力学参数对通气速率的变化规律。采用所确定的反应级数,根据连续操作下的动力学方程及Fe2+转化率随稀释率变化的关系确定了连续操作下的反应速率常数分别为0.9698h-1·(g·L-1)0.1666、0.9042h-1·(g·L-1)0.1135。动力学曲线与真实值之间的相关系数R2均在0.99以上,具有良好的预测性。 The rate of oxidation of ferrous iron in bio-oxidation reactor is the key factor constraining the entire biodesulfurizaion process. Wood chips of two different sizes were used as the immobiliazation carriers of Thiobacillus ferrooxidans, and the kinetics of oxidation of ferrous iron conducted by the biofilm was analyzed. According to the kinetic equation deduced, the data of ferrous iron concentration varying with reaction time was analyzed by the method of non-linear fitting. Thereby the reaction orders were obtained, when two different carders worked respectively at the optimal aeration rate. And the relationship between the kinetic parameters and the aeration rate were investigated when wood chips (b) was used as the carrier. According to the reaction orders obtained and the data of conversion of ferrous iron varying with the dilution rate under continuous operation, the reaction rate constants in the kinetic equation deducted were obtained by the method of linear fitting as follows, 0.9698h^-1·(g·L^-1)^0.1666、0.9042h^-1·(g·L^-1)^0.1135. The correlation coefficients between prediction model and experimental data were all higher than 0.99, indicating that the kinetic model was suitable for prediction.
出处 《化工进展》 EI CAS CSCD 北大核心 2009年第7期1237-1240,共4页 Chemical Industry and Engineering Progress
基金 国家自然科学基金资助项目(20576082)
关键词 氧化亚铁硫杆菌 二价铁 氧化动力学 Thiobacillusferrooxidans ferrous iron kinetics of oxidation
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  • 1赵地顺,刘翠微,马四国.FCC汽油模型化合物光催化氧化脱硫的研究[J].高等学校化学学报,2006,27(4):692-696. 被引量:31
  • 2陈娜,张文林,米冠杰,侯凯湖.FCC汽油萃取脱硫过程萃取剂筛选[J].化工进展,2006,25(11):1345-1348. 被引量:23
  • 3SELVAVATHI V, CHIDAMBARAM V, MEENAKSHISUNDARAM A, et al. Adsorptive desulfurization of diesel on activated carbon and nickel supported systems [J]. Catalysis Today, 2009, 141 (1-2) : 99-102.
  • 4JIANG Xue, LI Huaming, ZHU Wenshuai, et al. Deep desulfurization of fuels catalyzed by surfactant-type decatungstates using H2O2 as oxidant[J]. Fuel, 2009, 88 (3) : 431-436.
  • 5ZHOU Xinrui, LI Juan, WANG Xiuna, et al. Oxidative desulfurization of dibenzothiophene based on molecular oxygen and iron phthalocyanine [J]. Fuel Processing Technology, 2009, 90(2): 317-323.
  • 6ASGHAR M D, ZAHRA K, MOHAMMAD A S. Oxidative desulfurization of simulated light fuel oil and untreated kerosene [ J ]. Fuel Processing Technology, 2009, 90(3): 435-445.
  • 7单玉华 邬国英 李为民.氧化法精制汽油或柴油的方法[P].CN:99119904.2001-07-11.
  • 8刘帅,冯丽娟,侯影飞,于英民,王亮,李春虎.汽柴油氧化-萃取脱硫技术中萃取过程研究进展[J].精细石油化工进展,2008,9(9):28-31. 被引量:3

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