α-Zirconium phosphate (α-ZrP), a classical layered compound, has found widespread application. Exfoliation of α-ZrP has been mainly achieved by propylamine (PA) or tetrabutylammonium hydroxide (TBAOH), but the exact mechanism of exfoliation has not been completely elucidated. We examined the feasibility of exfoliation utilizing tetraalkylammonium hydroxide (TXAOH) and investigated the stepwise intercalation/exfoliation mechanism of α-ZrP. All of the TXAOHs examined (carbon number of the branches: 1−4) were able to exfoliate α-ZrP in an aqueous dispersion under ultrasonication. Furthermore, exfoliation of α-ZrP by two different exfoliators (either a mixture of two or sequentially) was also investigated to pinpoint the exfoliation mechanism. Our results indicate that small TXA cations are kinetically preferred to diffuse into the galleries of α-ZrP, while large TXA cations can help open up the galleries and facilitate transport of the already intercalated cations. These findings should help fellow researchers to choose the most suitable exfoliators for their own projects and develop better intercalation/exfoliation systems.

The exfoliation of microcrystalline α-zirconium phosphate (α-ZrP) in an organic solvent is very difficult to achieve. Surprisingly, the addition of tetra­(n-butyl)­ammonium hydroxide (TBAOH) into a methanol dispersion of a nanosized α-ZrP brings about the complete exfoliation of nanosheets. To understand the mechanism, we examined the stepwise intercalation/exfoliation of the nanosized α-ZrP using TBAOH in four different solvents (water, methanol, ethanol, and butanol). Propionate groups on the edge of the nanosized α-ZrP prevent TBA cations from entering the galleries. Due to the formation of unstable solvent-intercalated α-ZrP with an increased interlayer distance in methanol and ethanol, TBA cations can overcome the steric hindrance and move into nanosheet layers to exchange with solvent molecules. However, the movability of the cations into the center of the galleries is preferred at a certain interlayer distance range, which leads to exfoliation of α-ZrP in methanol but intercalation only in ethanol. In water, in the beginning, neither intercalation nor exfoliation by TBA cations occurs. An additional amount of TBAOH causes the deformation of propionate groups and removes the barriers on the edges, followed by late intercalation and then exfoliation. On the other hand, butanol, as the solvent, is bulky and effectively limits the intercalation behavior of TBA cations. The weaker polarity of ethanol and butanol, compared with water and methanol, lowers the ion interactions in the solvent, which is another reason why they do not lead to exfoliation.

Host–guest interaction, being reversible and stimuli-responsive, is ideal to be applied to the design of hydrogels. We created a gelation system based on the host–guest interactions between the adamantyl groups and β-cyclodextrin (β-CD) polymer. N,N,N-trimethyl-1-adamantylammonium hydroxide (TriMAA) cations were attached to the pre-exfoliated α-zirconium phosphate (α-ZrP) nanosheets by ionic bonding through a displacement reaction with the exfoliating agents. The exfoliated α-ZrP nanosheets with adamantyl groups directly or indirectly attached to the surface act as reversible high-functionality crosslinkers within the β-CD polymer. The gelation occurred at a host-to-guest ratio of 1:10 or 1:5 at room temperature within minutes. The agents used to exfoliate α-ZrP can tailor the surface of the resultant α-ZrP nanosheets and the ionic strength of the system, which directly affects the further gelation results. Plus, the exfoliating agent cations may generate a host-and-guest interaction with the β-CD polymer as well. This gelation process without covalent bonding formation should help fellow researchers to better understand the gelation system and host–guest interactions.

In this paper the uptake of carrier free ^'Sr from solution and subsequently its separation from '"Yttrium by an inorganic ion exchanger of the type of zirconium phosphate gels is presented. The uptake was determined by taking liquid aliquots at desired time intervals from solutions over various cationic forms of zirconium phosphate gels. The volume to solid ratio was kept 200. The results of kinetics and distribution coefficients revealed high selectivity for ^Sr from ^Y in all forms of zirconium phosphate gels. Cerenkov counting was used to observe the initial and final radioactivity in the liquid phase. All the ion exchange experiments were carried out at room temperature. The radioactivity in each case was corrected for the background counts.