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陶瓷级二氧化铀的脱氟动力学
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作者 宋正孝 谌竟清 +2 位作者 牛文泰 谢振风 葛庆仁 《核科学与工程》 CSCD 北大核心 1996年第2期189-192,153,共5页
陶瓷级二氧化铀的脱氟动力学宋正孝,谌竟清,牛文泰,谢振风,葛庆仁(天津大学)关键词二氧化铀,脱氟动力学1前言核动力堆所需的陶瓷级二氧化铀通常以六氟化铀为起始原料,在其一系列的转化加工过程中,其中间产物及最终产品不可避... 陶瓷级二氧化铀的脱氟动力学宋正孝,谌竟清,牛文泰,谢振风,葛庆仁(天津大学)关键词二氧化铀,脱氟动力学1前言核动力堆所需的陶瓷级二氧化铀通常以六氟化铀为起始原料,在其一系列的转化加工过程中,其中间产物及最终产品不可避免地要带有一定量的残留氟。这些残留... 展开更多
关键词 陶瓷级二氧化铀 脱氟动力学 烧结性能 反应堆 核安全
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镁基活性氧化铝的制备及脱氟性能研究
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作者 范茂盛 裴启飞 +1 位作者 陆占清 杨坤 《昆明理工大学学报(自然科学版)》 北大核心 2023年第6期1-7,共7页
针对现行改性活性氧化铝吸附剂尚未有系统研究,对工业指导性弱等问题,本文以实际含氟废水为考察对象,对比考察了多种改性剂种类的影响,优选制备镁基活性氧化铝,并利用Pseudo-First-Order(PFO)和Pseudo-Second-Order(PSO)非线性模型对其... 针对现行改性活性氧化铝吸附剂尚未有系统研究,对工业指导性弱等问题,本文以实际含氟废水为考察对象,对比考察了多种改性剂种类的影响,优选制备镁基活性氧化铝,并利用Pseudo-First-Order(PFO)和Pseudo-Second-Order(PSO)非线性模型对其脱氟机理进行模拟研究.研究结果表明,相较锌、钙、镧改性,硫酸镁改性能明显提高活性氧化铝对氟的吸附性能.当硫酸镁浓度为0.05 mol/L、液固比为8、焙烧温度为350℃,吸附剂中出现活性相AlOOH和MgAl_(2)(OH)_(8),除氟能力达到最佳.采用此层状镁基活性氧化铝吸附剂去除废液氟时,在吸附时间2.5 h、除氟温度70℃时,氟脱除率和平衡吸氟量达到最佳,分别为70.70%和8.36 mg/g,且吸附废液氟离子过程遵循PSO模型,吸附过程为镁基活性氧化铝吸附剂表面物质与废液中氟离子发生化学反应. 展开更多
关键词 镁基活性氧化铝 改性活性氧化铝吸附剂 机理 脱氟动力学
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An environmentally benign and sustainable process for carbon recovery and efficient defluorination of spent carbon cathode 被引量:4
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作者 Yi-fan LI Hao CHENG +3 位作者 Pei-yu GONG Kai YANG Zhong-liang TIAN Yan-qing LAI 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2022年第11期3810-3821,共12页
A systematic and green low-temperature sulfation roasting−water leaching strategy was put forward to achieve a very high fluorine removal rate of 97.82%for spent carbon cathode(SCC),which was believed as a hazardous s... A systematic and green low-temperature sulfation roasting−water leaching strategy was put forward to achieve a very high fluorine removal rate of 97.82%for spent carbon cathode(SCC),which was believed as a hazardous solid waste.And the carbon could be recycled with a purity of 90.29 wt.%in the flaky microstructure.Thermodynamic analysis and the results of SEM,XRD and EDS indicate that most of the fluoride could convert into water-soluble sulfate at low temperature.And the highest fluorine removal rate could be obtained when<0.15 mm SCC particles were mixed with sulfuric acid at a liquid-to-solid ratio of 1:1,and then roasted at 300℃ for 0.5 h.The sulfate was removed to purify the carbon via water-leaching process.Avrami exponents and corresponding activation energy for the roasting and leaching process demonstrated that both processes are controlled by diffusion. 展开更多
关键词 spent carbon cathode DEFLUORINATION sulfation roasting water-leaching kinetics analysis
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Thermodynamics and kinetics of fluoride removal from simulated zinc sulfate solution by La(Ⅲ)-modified zeolite 被引量:12
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作者 Yan-qing LAI Kai YANG +3 位作者 Chao YANG Zhong-liang TIAN Wei-chang GUO Jie LI 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2018年第4期783-793,共11页
To understand the mechanism of fluoride removal from the simulated zinc sulfate solution by the La(III)-modified zeolite,the adsorbent was characterized by XRD,SEM and EDS.The effects of absorbent dose and contact tim... To understand the mechanism of fluoride removal from the simulated zinc sulfate solution by the La(III)-modified zeolite,the adsorbent was characterized by XRD,SEM and EDS.The effects of absorbent dose and contact time,the adsorption isotherms and the sorption kinetics were investigated.The experimental results were compatible with the Langmuir isotherm model.The theoretical maximum adsorption capacities are 20.83 and 23.04 mg/g at 303 and 313 K,respectively.And the physisorption is revealed using the Temkin isotherm model and the D-R isotherm model.The sorption process is more suitable by the pseudo-second-order kinetic models.Thermodynamic parameters such as standard free energy change(ΔGΘ<0 kJ/mol),standard enthalpy change(ΔHΘ=8.28 kJ/mol)and standard entropy change(ΔSΘ=0.030 kJ/(mol?K))indicate the spontaneity of adsorption and endothermic physical sorption.Furthermore,the fluoride concentration in the industrial zinc sulfate solution decreases from 98.05 to 44.09 mg/L with the adsorbent dosage of 15 g/L. 展开更多
关键词 La(III)-modified zeolite fluoride removal zinc sulfate solution adsorption isotherm KINETICS
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Defluorination of Wet-Phosphoric Acid: Equilibrium and Kinetic Studies
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作者 Hayet Omri Narjés Harrouch Batis 《Journal of Chemistry and Chemical Engineering》 2014年第2期204-213,共10页
This study describes the advantages of using iron-oxide-pillared MF (montmorillonite) and EDTA (ethylenediaminetetraacetic acid)-pillared MD (montmorillonite) for the removal of fluoride in the phosphoric acid. ... This study describes the advantages of using iron-oxide-pillared MF (montmorillonite) and EDTA (ethylenediaminetetraacetic acid)-pillared MD (montmorillonite) for the removal of fluoride in the phosphoric acid. The MF and MD were characterized by using BET (Brunauer-Emmett-Teller) and SEM (scanning electron microscope) for there to appreciate their textural and structural properties and in order to appraise their capacity in the fixation of the fluorine experimental results of fluorine adsorption show a defluoration of the phosphoric acid passing beyond 90% with both clays with a light performance for the MD. The kinetics of fluorine adsorption on MF and on MD has been measured at different temperatures. Indeed, the adsorbed quantity increases more favorably to temperatures more high. This kinetics could be described by two models: pseudo-first-order or pseudo-second-order, which depends on temperature and the nature of adsorbent. At different temperatures used and with various adsorbents (MD and MF, the pseudo second order model was the most reliable to determine the order of kinetics of adsorption of fluorine, which is also reflected a good correlation coefficient (above 0.99). The fluoride sorption was reasonably explained with Langmuir or Freundlich isotherms. Thermodynamic parameters such as AG~, AH~, AS~ and kinetic one E,, (apparent activation energy) were calculated in order to understand the nature of sorption process. Results indicate that the mechanism of adsorption of the ion of fluoride on the pillared montmorillonite is an exothermic reaction. During equilibrium conditions, both the systems showed negative Gibbs energy, which indicates stability of system. The values of apparent activation energy for the both clays show that the adsorption of F ions is easier on the MF. 展开更多
关键词 Phosphoric acid adsorbing defluoration MONTMORILLONITE kinetic.
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