The adsorption of D-glucosamine (2-amino-2-deoxy-D-gIucose) in the protonated or neutral form on homoionic Cu2+-bentonite was investigated by infrared (IR) and electron spin resonance (ESR) spectroscopy and chemical analyses of solution. The results show that the interaction of the glucosamine hydrochloride with the clay complexed a small fraction of interlayer metal ions with neutral amino sugar molecules. In contrast, the adsorption of free glucosamine was much more favorable and resulted in interlayer copper(II) complexes, mainly those in which the ligand was coordinated through amino and deprotonated hydroxyl groups. Part of the amino sugar molecules, however, were transformed into glucosammonium, replacing copper as the saturating ion.

Phenamiphos interacted with homoionic montmorillonites of Ca2+, Mn2+, Co2+, and Ni2+ to form interlayer complexes having basal spacings of about 16.5 Å. In the infrared spectra, the ν-PO bands were displaced towards lower frequencies suggesting that this group interacted with the exchange cations. Moreover, a small shoulder at 1600 cm−1 indicated the partial protonation of the phenamiphos. After heating the complexes to 110°, 160°, and 200°C, however, the bands corresponding to δ-NH2+ and ν-NH intensified because of increased protonation, whereas the ν-PO bands had the same intensity as in pure phenamiphos. The fundamental implication of these observations is that phenamiphos interacts with exchange cations through molecules of coordinated water, possibly by means of the P=O group.

The infrared absorption spectra of a palygorskite sample from Cáceres, Spain, showed two previously unreported bands in the OH-stretching region at 3420–3440 and 3220–3230 cm−1 after evacuation at 90°–230°C. These bands, which reached maximum intensity after the sample was heated at 150°C, were assigned to OH in the

$$\begin{array}{*{20}{c}} H \\: \\ {Si - O - Si\,and\,} \\ \end{array}\begin{array}{*{20}{c}} H \\: \\ {Si - O - A1} \\ \end{array}$$

The strongly coloured Cu-triethylenetetramine complex (Cu-Trien) provides a fast and easy way to measure the cation exchange capacity of clay samples, but the reliability of this method has been questioned in recent publications. This work identifies several reasons for the poor reliability, thus improving both the precision and accuracy of the CEC method. Pure Trien is shown here to intercalate as does the Cu-Trien complex. Hence, the purity of Trien and also the Cu/Trien ratio require special attention. Using cold Cu-Trien solutions produces systematic deviations in CEC determinations caused by errors in the pipetted volumes. The present study demonstrates, for the first time, that the Cu-Trien complex protonates and changes its effective charge beyond 2+. Based on titration experiments at three different temperatures, a correction function is derived for calculating the total charge of the Cu-Trien complex as a function of pH. Accounting for these pH-corrected charges indicates that Cu-Trien may well be insensitive to edge charges on smectite. Finally, it is shown here that the ratio of sample mass to the initial amount of Cu-Trien is critical because excess adsorption of Cu-Trien in addition to CEC sensu strictu was observed.