Adsorption of dimeric surfactants in lamellar silicates

被引:4
|
作者
Balcerzak, Mateusz [1 ]
Pietralik, Zuzanna [1 ]
Domka, Ludwik [2 ]
Skrzypczak, Andrzej [3 ]
Kozak, Maciej [1 ]
机构
[1] Adam Mickiewicz Univ, Fac Phys, Dept Macromol Phys, PL-61614 Poznan, Poland
[2] Adam Mickiewicz Univ, Fac Chem, Dept Metalorgan Chem, PL-60780 Poznan, Poland
[3] Poznan Univ Tech, Inst Chem Technol, PL-60965 Poznan, Poland
关键词
Gemini surfactant; Dicationic surfactant; Montmorillonite; Adsorption; Organophilisation; MONTMORILLONITE; ORGANOCLAYS; CLAY; BEHAVIOR;
D O I
10.1016/j.nimb.2015.07.135
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
The adsorption of different types of cationic surfactants in lamellar silicates changes their surface character from hydrophilic to hydrophobic. This study was undertaken to obtain lamellar silicates modified by a series of novel dimeric (gemini) surfactants of different length alkyl chains and to characterise these organophilised materials. Synthetic sodium montmorillonite SOMASIF (R) ME 100 (M) and enriched bentonite of natural origin (Nanoclay - hydrophilic bentonite (R)) were organophilised with dimeric (gemini) surfactants (1,1'-(1,4-butanediyl)bis(alkoxymethyl)imidazolium dichlorides). As a result of surfactant molecule adsorption in interlamellar space, the d-spacing (d(001)) increased from 0.97 nm (for the anhydrous structure) to 2.04 nm. A Fourier transform infrared spectroscopy (FTIR) analysis of the modified systems reveals bands assigned to the stretching vibrations of the CH2 and CH3 groups and the scissoring vibrations of the NH group from the structure of the dimeric surfactants. Therrnogravimetric (TG) and derivative thermogravimetric (DTG) studies imply a four-stage process of surfactant decomposition. Scanning electron microscopy (SEM) images provide information on the influence of dimeric surfactant intercalation into the silicate structures. Particles of the modified systems show a tendency toward the formation of irregularly shaped agglomerates. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:108 / 115
页数:8
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