Abstract
The possibility of enriching in (17)O the water molecules within hydrated biominerals belonging to the Ca-pyrophosphate family was investigated, using liquid assisted grinding (LAG) in the presence of (17)O-labelled water. Two phases with different hydration levels, namely triclinic calcium pyrophosphate dihydrate (Ca(2)P(2)O(7)·2H(2)O, denoted t-CPPD) and monoclinic calcium pyrophosphate tetrahydrate (Ca(2)P(2)O(7)·4H(2)O, denoted m-CPPT β) were enriched in (17)O using a "post-enrichment" strategy, in which the non-labelled precursors were ground under gentle milling conditions in the presence of stoichiometric quantities of (17)O-enriched water (introduced here in very small volumes ∼10 μL). Using high-resolution (17)O solid-state NMR (ssNMR) analyses at multiple magnetic fields, and dynamic nuclear polarisation (DNP)-enhanced (17)O NMR, it was possible to show that the labelled water molecules are mainly located at the core of the crystal structures, but that they can enter the lattice in different ways, namely by dissolution/recrystallisation or by diffusion. Overall, this work sheds light on the importance of high-resolution (17)O NMR to help decipher the different roles that water can play as a liquid-assisted grinding agent and as a reagent for (17)O-isotopic enrichment.