Kinetics, isotherms and thermodynamic evaluation of amine functionalized magnetic carbon for methyl red removal from aqueous solutions

被引:127
作者
Saleh, Tawfik A. [1 ]
Al-Absi, Akram A. [2 ]
机构
[1] King Fahd Univ Petr & Minerals, Chem Dept, Dhahran 31261, Saudi Arabia
[2] King Fahd Univ Petr & Minerals, Chem Engn Dept, Dhahran 31261, Saudi Arabia
关键词
Modified carbon; Typical branched polyethylenimine; Column breakthrough; ACTIVATED CARBON; PHOTOCATALYTIC DEGRADATION; ADSORPTION; BLUE; WASTE; WATER; DYE; EQUILIBRIUM; ADSORBENT; SORPTION;
D O I
10.1016/j.molliq.2017.10.064
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Global fresh water demand increases as population increases. Thus, the demand for cost-effective materials and efficient technologies for water treatment is on the rise. Here, we modified rubber-derived carbon by iron oxide and then the obtained material was subjected to surface modification using typical branched polyethylenimine (BPEI) to produce a magnetic composite of AC-FexOrBPEI. The composite was characterized. The efficiency of the polymer anchored material was examined for methyl red (MR) removal from aqueous media in the batch and column systems. The results indicated a high percentage of removal (approximate to 100%) and eequilibrium was observed in 10 mins. The process followed models of the Langmuir isotherm and Pseudo -second order, with a capacity of 526 mg/g. The negative standard enthalpy change (Delta H degrees) suggests that the adsorption of MR on the material is exothermic. The breakthrough was observed after 150 mins using a 1 mM concentration of methyl red flow through a designed short column. The AC-FexOy-BPEI demonstrated remarkable efficiency in removing MR from aqueous solutions. The high adsorption capacity does indeed make the amine -modified material as an effective sorbent. The material leverages its cost-effective source, in addition to the ease of preparation along with its fast uptake capacities, it offers great promise for wastewater remediation. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:577 / 585
页数:9
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