PFG NMR studies of lysine–silica solutions

Abstract

The formation process of silica nanoparticles in lysine–silica mixtures was studied using dynamic light scattering (DLS) and pulsed-field gradient (PFG) NMR measurements. 1H NMR shows line broadening of the lysine resonances during TEOS hydrolysis/nanoparticle formation. Analysis of the TEOS hydrolysis kinetics show that TEOS hydrolysis is the rate-limiting step in particle formation, and has an activation energy of 20.5kJ/mol. Transverse relaxation measurements show a corresponding decrease in T2 with TEOS hydrolysis, indicating a reduction in the lysine mobility due to lysine–silica interactions. PFG NMR results indicate a systemic decrease in the self-diffusion coefficient of lysine as particle formation proceeds. The results obtained can be described using a two-state model wherein lysine is either free in solution or bound to the nanoparticles. Analysis of the PFG data of samples made at various temperatures show that lysine coverage upon complete hydrolysis is between 2.5 and 2.8mmollysine/kg solution, and insensitive to the heating temperature. PFG NMR shows a linear increase in the amount of bound lysine with increasing lysine content, indicating an increase in the surface area present, i.e. more and smaller particles, with increased lysine content. The PFG NMR results presented give quantitative insights that indicate that while pH is likely the primary driver for the rate of particle formation and particle size, lysine is critical for stabilization of the nanoparticles.