Kinetic and equilibrium studies of adsorption of acid blue dye onto preformed flocs as adsorbents

IF 1.5 4区 化学 Q4 CHEMISTRY, PHYSICAL
Nijagala Munilakshmi, Muduru Srimurali, Janakiram Karthikeyan, Charmathi Nagaraju
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引用次数: 0

Abstract

Adsorption studies of decolorization of Acid blue dye by using novel adsorbents of preformed flocs of Aluminum Sulphate, Ferric Chloride, and Ferrous Sulphate were carried out through non-flow batch sorption studies. The influence of pH, equilibrium contact time, and floc dose on color removal was studied. Kinetic and equilibrium studies were carried out to know the efficacy of adsorbents in the decolorization of an aqueous solution of C.I. Acid blue 113 dye. In order to probe into the mechanism involved in the decolorization of dye solution, FTIR and SEM studies were conducted. The Langmuir isotherm was well fitted to the equilibrium data implying that there is monolayer formation in the process of sorption. Kinetic data fitted well to pseudo second order which states that chemisorption is the rate limiting step in the adsorption process. The adsorption capacity of preformed flocs of aluminum sulphate, ferric chloride, and ferrous sulphate were found to be 450 mg/g, 500 mg/g, and 125 mg/g. FTIR and SEM studies shows that there is adsorbent-dye complex formation in the adsorption process of decolorization of Acid dye with preformed flocs.

预成型絮凝体作为吸附剂对酸性蓝染料吸附的动力学和平衡研究
采用非流动间歇吸附法,对硫酸铝、氯化铁和硫酸亚铁预成型絮凝体的新型吸附剂对酸性蓝染料的脱色进行了吸附研究。研究了pH、平衡接触时间和絮凝剂用量对去色的影响。通过动力学和平衡研究了解了吸附剂对C.I.酸蓝113染料水溶液的脱色效果。为了探讨染料溶液脱色的机理,进行了红外光谱和扫描电镜研究。Langmuir等温线很好地拟合了平衡数据,表明吸附过程中存在单分子层的形成。动力学数据符合准二级,表明化学吸附是吸附过程中的限速步骤。预成型絮凝体对硫酸铝、氯化铁和硫酸亚铁的吸附量分别为450 mg/g、500 mg/g和125 mg/g。红外光谱(FTIR)和扫描电镜(SEM)研究表明,预成型絮凝体对酸性染料的脱色吸附过程中存在着色剂-染料络合物的形成。
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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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