Removal of methyl orange from aqueous solutions using a bentonite modified with a new gemini surfactant

被引:61
作者
Kan, Taotao [1 ]
Jiang, Xiaohui [1 ]
Zhou, Limei [1 ]
Yang, Mei [1 ]
Duan, Ming [2 ]
Liu, Pingli [2 ]
Jiang, Xiaomin [3 ]
机构
[1] China W Normal Univ, Key Lab Chem Synth & Pollut Control, Nanchong 637009, Sichuan, Peoples R China
[2] SW Petr Univ, State Key Lab Oil & Gas Reservoir Geol & Exploita, Chengdu 610500, Sichuan, Peoples R China
[3] SW Elect Power Design Inst, Chengdu 610021, Sichuan, Peoples R China
关键词
Gemini surfactant-modified bentonite; Methyl orange; Adsorption; Decoloration; COD removal; CATIONIC SURFACTANTS; ADSORPTION; ORGANOCLAYS; SORPTION; PHENOL; ORGANOBENTONITE; MONTMORILLONITE; HYDROCARBONS; INTERFACE; WATER;
D O I
10.1016/j.clay.2011.07.009
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
Glycol bis-N-cetylnicotinate dibromide (designated as GN16-1-16), a new cationic gemini surfactant, was prepared and used to modify bentonite. Bentonite modified with commercial cetyltrimethylammonium bromide (CTMAB) was also prepared for comparison purposes. FTIR and XRD revealed that both surfactants successfully intercalated into the bentonite layers. The basal spacing was 2.65 nm for GN-Bt (the bentonite modified by GN16-1-16) and 2.14 nm for C-Bt (the bentonite modified by CTMAB), indicating that GN16-1-16 was more efficient than CTMAB in expanding the interlayer space of montmorillonite. The optimum reaction time and temperature in the modification were 1 h and 30 degrees C for GN16-1-16 and 3 h and 70 degrees C for CTMAB. The GN16-1-16 reacted with bentonite faster than CTMAB. The decoloration rate and the COD removal of methyl orange (MO) solution were 99.02% and 90.62% for GN-Bt and 80.12% and 75.49% for C-BT. Therefore, GN-Bt was more effective than C-Bt to remove MO from aqueous solution. However, the efficiency of GN-Bt decreased rapidly at pH>6, which might be due to the hydrolysis of the ester groups in GN16-1-16 molecule under alkaline environment. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:184 / 187
页数:4
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