Abstract
To establish an approach for a bulk upscaling of a composit material consisting of calcium carbonate and tunable peptoids we
here combined three distinct approaches to thoroughly access the underlying
kinetic and thermodynamic driving forces for CaCO3 formation on peptoid polymers.
We derived the net interfacial free energy for calcite formation on the
nanosheets and self-assemblage monolayers of the sheets constituent functional
groups (carboxyl, amine and a 1:1 mix) using: nucleation experiments, dynamic
force spectroscopy and theoretical modeling (COSMO-RS). We applied nucleation theory to the results and obtain insight into conditions were we can obtain favorable nucleation conditions on the polymers in a highly controlled manner.
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