摘要
We report a molecular modeling paradigm to describe silica polymerization reactions in aqueous solutions at conditions that are representative of realistic experimental processes like biosilicification or porous silica synthesis–i.e.at close to ambient temperatures and over a wide range of pH.The key point is to describe the Si-O-Si chemical bond formation and breakage processes through a continuous potential with a balance between attractive and repulsive interactions between suitably placed virtual sites and sticky particles.The simplicity of the model,its applicability in standard parallelized molecular dynamics codes,and its compatibility with the widely used MARTINI coarse-grained force-field allows for the study of systems containing millions of atoms over microsecond time scales.The model is calibrated to match experimental results for the temporal evolution of silica polymerization in aqueous solution close to the isoelectric point,and can describe silica polymerization and self-assembly processes during encapsulation of a surfactant micelle.
基金
the Portuguese Fundação para a Ciência e a Tecnologia(FCT/MCTES)
co-financed by the European Regional Development Fund(FEDER)under the PT2020 Partnership Agreement
project ref.QS-2019-2-0034 financed by the Red Española de Supercomputación(RES).
