Trapping characteristic of halloysite lumen for methyl orange

被引:34
作者
Chen, Hao [1 ]
Yan, Hua [1 ]
Pei, Zhenzhao [2 ]
Wu, Junyong [1 ]
Li, Rongrong [1 ]
Jin, Yanxian [1 ,2 ]
Zhao, Jie [1 ]
机构
[1] Taizhou Univ, Sch Pharmaceut & Chem Engn, Taizhou 318000, Peoples R China
[2] Hebei Univ Engn, Dept Chem, Handan 056038, Peoples R China
基金
中国国家自然科学基金;
关键词
Halloysite nanotubes; Methyl orange; Trapping property; Mechanism; LOW-COST ADSORBENTS; AQUEOUS-SOLUTIONS; CLAY NANOTUBES; DYE REMOVAL; ADSORPTION; RED; INTERCALATION; AGGREGATION; COMPOSITE; RELEASE;
D O I
10.1016/j.apsusc.2015.04.167
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
The interaction of clay minerals and dyes is an area of great interest especially in the development of novel adsorbents. In this report, we demonstrated interaction of halloysite nanotubes (HNTs) and an anionic dye, methyl orange (MO), through a electrostatic attraction. Halloysite lumen has a trapping characteristic for methyl orange, which is mainly determined by the positively charged nature of the inner surface of HNTs. XRD results confirmed that intercalation of methyl orange into HNTs did not occur. SEM-EDS and photostability results showed that MO molecules were primarily in HNTs lumen. Adsorption isotherm studies revealed an interesting phenomenon, i.e., a sudden increase of adsorption capacity occurred in the initial dye concentration of about 75 mg/L, which was just the dye concentration corresponding to the onset of dye oligomer formation. This suggested dye aggregation state had a decisive influence to the adsorption behavior of MO on the halloysite. BET results demonstrated at low and high dye concentrations, single MO molecule and aggregation of several dimers through hydrophobic interaction, interacted with Al-OH2+ sites on the inner wall, respectively. Desorption experiments showed that MO in HNTs can be completely removed with deionized water, indicating halloysite is a low-cost and efficient adsorbent for anionic dye. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:769 / 776
页数:8
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