Kinetic study of polydopamine sphere synthesis using TRIS: relationship between synthesis conditions and final properties

The synthesis and characterization of polydopamine (PDA) using dopamine (DA) as the monomer and (hydroxymethyl)aminomethane (TRIS) as the oxidant is studied. The effect of temperature and TRIS concentration on the kinetics of dopamine polymerization is evaluated, and the kinetic parameters are also calculated. Three TRIS concentrations are used to assess their effect on DA polymerization kinetics. The reaction at 1.5 mmol of TRIS shows a sustained increase of the rate constant with temperature from 2.38 x 10(-4) to 5.10 x 10(-4) when the temperature is increased from 25 to 55 degrees C; however, not all reactions follow an Arrhenius law. In addition, the correlation between the synthesis parameters and morphological, structural, and thermal properties of polydopamine is established. The morphology of the PDA particles is evaluated by Scanning Electron Microscopy (SEM), the relationships between the diameter, distribution size, and the rate constant. Thermal characterization by Differential Scanning Calorimetry (DSC) shows an endothermic transition around 130 degrees C associated with the melting of PDA's regular structure. It is supported by structural studies, such as infrared and Raman spectroscopy and X-ray Diffraction (XRD), by observing a broad peak at 23.1 degrees (2 theta) that fits with a graphitic-like structure of PDA.

Automated summary

This study investigates the synthesis and characterization of polydopamine (PDA) using dopamine (DA) as the monomer and (hydroxymethyl)aminomethane (TRIS) as the oxidant. The effect of temperature and TRIS concentration on the kinetics of dopamine polymerization is evaluated, and the correlation between the synthesis parameters and morphological, structural, and thermal properties of polydopamine is established. Scanning Electron Microscopy (SEM) and Differential Scanning Calorimetry (DSC) are utilized to evaluate the morphology and thermal behavior of PDA, respectively. Structural studies using infrared and Raman spectroscopy, as well as X-ray Diffraction (XRD), confirm the graphitic-like structure of PDA.