The negative surface charge of synthetic allophanes with a range of Si/Al ratios decreased and positive charge increased with increasing alumina content at a given pH. The phosphate adsorption capacity also increased with increasing Al content. That this relationship between composition and chemical reactivity was not found for the soil allophanes is attributed to the presence of specifically adsorbed organic or inorganic anions on the natural material. Both synthetic and natural imogolites had a much lower capacity to adsorb phosphate than the allophanes and adsorbed anomalously high amounts of Cl− and ClO4− at high pH. It is proposed that intercalation of salt occurs in imogolite, although electron spin resonance studies using spin probes failed to reveal the trapping of small organic molecules in imogolite tubes. These spin probes in the carboxylated form did, however, suggest an electrostatic retention of carboxylate by imogolite and a more specific adsorption by allophane involving ligand exchange of surface hydroxyl. The results illustrate the inherent differences in charge and surface properties of allophane and imogolite despite the common structural unit which the two minerals incorporate.

As 1:1 dioctahedral clay minerals, kaolinite and halloysite have similar chemical compositions. However, halloysite often possesses a nanotubular structure and special surface reactivity compared to platy kaolinite. The objective of this current work was to determine the effect of the SiO2/Al2O3 ratio on the microstructure and properties of geopolymers derived from two kinds of kaolin: platy kaolinite and nanotubular halloysite. The chemical structures and compositions of the geopolymers obtained were characterized through X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, and nuclear magnetic resonance (NMR), whereas the microstructural analysis was performed by scanning electron microscopy (SEM), the Brunauer–Emmett–Teller (BET) method, and N2 physisorption analysis. The results indicated that calcined halloysite showed greater geopolymerization reactivity than calcined kaolinite. In addition, the mechanical properties of the clay-based geopolymers depended not only on the SiO2/Al2O3 ratio but also on the morphology of the clay. Crystalline zeolite A and geopolymer were produced after alkali-activation of kaolin with a SiO2/Al2O3 ratio of 2.5; these products possessed porous and heterogeneous microstructures having poor compressive strength. As SiO2/Al2O3 ratios increased to >2.5, geopolymers with compact microstructure and high compressive strength were produced after alkali-activation of kaolin. Notably, at a given condition, halloysite-based geopolymers exhibited greater early compressive strength, more compactness, and more homogeneous microstructure than kaolinite-based geopolymers. This can be attributed to the nanotubular microstructure of halloysite, which can release more Si and Al during alkali activation than platy kaolinite. These results indicated that the various morphologies and microstructures among clays have significant impact on the microstructure and compressive strength of geopolymers.