Breen C, Watson R
Materials Research Institute, Sheffield Hallam University, Sheffield, S1 1WB, United Kingdom
J Colloid Interface Sci. 1998 Dec 15;208(2):422-429. doi: 10.1006/jcis.1998.5804.
The uptake curves for the adsorption of a polycation ([CH2CH(OH)CH2N(CH3)2]n+n(Cl)n-n) onto a low iron Texas bentonite, WL, have been determined and compared with those onto two source smectites, SWy-1 and SAz-1. The polycation exhibited a marked affinity for all the smectite surfaces but polycation uptake was maximized on the fine fractions of Na+-WL. Variable temperature X-ray diffraction of the clay polycation complexes showed that the polycation was segregated into different interlayers at loadings below 30% of the CEC. The adsorption of benzene onto TMA+-exchanged SWy-1, SAz-1, and WL showed that, despite having a comparable layer charge to SWy-1, WL was as poor a sorbent for benzene as SAz-1, which has a much higher layer charge. The adsorption of p-nitrophenol (PNP) from aqueous solution onto the TMA+-exchanged sorbents exhibited the same trends, although a smaller amount was adsorbed due to the greater size of PNP. The amount of PNP adsorbed by polycation-treated SWy-1 depended upon the polycation loading, and PNP uptake maximized at loadings of 28 and 46 mg (g clay)-1. At higher loadings (80, 102, and 147 mg (g clay)-1) the uptake curves became linear and the PNP uptake decreased with increased polycation loading. No polycation-treated clay was as effective as TMA+-exchanged SWy-1 for the removal of PNP from water. Copyright 1998 Academic Press.
