Synthesis and Hydrophilicity Analysis of bis(propane‐1,2‐diol) Terminated Polydimethylsiloxanes (PDMSs)

Abstract

Among silicone oligomers, polydimethylsiloxane (PDMS) is widely used industrially and has the advantage of improving the properties of other compounds, such as flame‐retardant polyurethane (PU). However, as there are barriers to the synthesis of PU‐grafted siloxane, owing to the polarity difference between isocyanate and PDMS, numerous research efforts are being aimed at improving the hydrophilicity of PDMS. To improve the hydrophilicity and reactivity of hydroxyl PDMS, bis(propane‐1,2‐diol)‐terminated PDMS (G‐PDMS‐G) with four hydroxy (‐OH) groups was synthesized through ring‐opening addition to replace both ends of linear α,ω‐hydroxyl PDMS (HO‐ PDMS‐OH) with glycidol, resulting in hydrophilic PDMS rather than dihydroxy PDMS. In all cases of G‐PDMS‐G, the contact angle and viscosity both decreased by more than 20%, confirming the improved hydrophilicity. In particular, G‐PDMS‐G‐3, which has the largest molecular weight, demonstrated the greatest decrease in viscosity and contact angle (33%).