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作 者:严振 邱兆富[1] 金锡标 王远 刘畅 杨骥[1] YAN Zhen;QIU Zhaofu;JIN Xibiao;WANG Yuan;LIU Chang;YANG Ji(State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process,East China University of Science and Technology,Shanghai 200237,China)
机构地区:[1]华东理工大学资源与环境工程学院,国家环境保护化工过程环境风险评价与控制重点实验室,上海200237
出 处:《无机盐工业》2024年第1期81-89,95,共10页Inorganic Chemicals Industry
基 金:国家环境保护公益性行业科研资助项目(201309021)。
摘 要:为深度处理水中的三价锑[Sb(Ⅲ)]和五价锑[Sb(Ⅴ)],采用共沉淀法合成铈(Ce)、铁(γ-Fe_(2)O_(3))负载的4A分子筛新型吸附剂(4A@Ce-Fe)。Ce和γ-Fe_(2)O_(3)的负载显著提高了4A分子筛对锑的吸附能力,当铈铁质量比为1∶3、p H=7.0时,4A@Ce-Fe对Sb(Ⅲ)和Sb(Ⅴ)的最大吸附容量分别为50.50 mg/g和10.03 mg/g。4A@Ce-Fe的饱和磁化强度为23.70 emu/g,有良好的磁分离性能。Langmuir等温线模型可以更好地拟合Sb(Ⅲ)的吸附,而Langmuir和Freundlich两种等温线模型都能很好地拟合Sb(Ⅴ)的吸附。吸附动力学数据拟合表明,Sb(Ⅲ)和Sb(Ⅴ)的吸附更符合准二级动力学模型。4A@Ce-Fe在初始pH为4.0~10.0时有较好的吸附效果,Ce、Fe几乎没有溶出;共存Cl^(-)、SO_(4)^(2-)和NO_(3)^(-)对Sb(Ⅲ)和Sb(Ⅴ)的吸附效果影响较小,而共存HCO_(3)^(-)和H_(2)PO_(4)^(-)的影响则较大。XRD、SEM、BET、FTIR、XPS等测试结果表明,Sb(Ⅲ)和Sb(Ⅴ)在4A@Ce-Fe上可能的吸附机理包括离子交换、表面络合和氧化还原反应,其中M—O—Sb配合物的形成对Sb的吸附起主要作用。In order to efficiently remove Sb(Ⅲ)and Sb(V)from water,a new type of Ce and Fe-loaded 4A molecular sieve adsorbent(4A@Ce-Fe)was synthesized by coprecipitation method.Ce andγ-Fe_(2)O_(3)loading significantly improved the ad⁃sorption capacity of molecular sieve for antimony.When the Ce∶Fe mass ratio was 1∶3 and pH was 7.0,the maximum ad⁃sorption capacity of 4A@Ce-Fe for Sb(Ⅲ)and Sb(V)was 50.50 mg/g and 10.03 mg/g,respectively.The saturation magne⁃tization of 4A@Ce-Fe was 23.70 emu/g,which had good magnetic separation performance and was easy to separate from wa⁃ter.Langmuir isotherms could well fit the adsorption of Sb(Ⅲ)and Sb(V),and Langmuir and Freundlich isotherms could well fit the adsorption data of Sb(V).The adsorption kinetics study showed that the adsorption of Sb(Ⅲ)and Sb(V)was more in line with the pseudo⁃second⁃order kinetic model.The adsorbent had good adsorption effect on antimony at the initial pH=4.0~10.0,and Ce and Fe were hardly dissolved out.Cl^(-),SO_(4)^(2-)and NO_(3)^(-)had little effect on the adsorption of Sb(Ⅲ)and Sb(V),and the presence of HCO_(3)^(-)and H_(2)PO_(4)^(-)significantly reduced the adsorption capacity.XRD,SEM,BET,FT-IR,XPS and other test results showed that the possible adsorption mechanisms of Sb(Ⅲ)and Sb(V)on 4A@Ce-Fe included ion exchange,surface complexation and oxidation-reduction reaction.The formation of M—O—Sb complex played a major role in Sb adsorption.
关 键 词:4A分子筛 铈负载 γ-Fe_(2)O_(3)负载 锑吸附
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