The aminolysis of styrene–maleic anhydride copolymers for a new modifier used in urea-formaldehyde resins

Abstract

Styrene (St) and maleic anhydride (MA) alternating copolymers with different molecular weights (MW) were synthesized via radical copolymerization. The copolymers were subsequently transferred into water-soluble maleic amic acid derivatives (SMAA) via the aminolysis of anhydride groups using (NH4)2CO3 as the ammonia sources. The synthesized polymers were applied as a new kind of macromolecular modifier and added into the reaction system during the synthesis of urea-formaldehyde (UF) resins via the traditional alkaline–acidic–alkaline three-step process. The UF resins modified with SMAA were characterized using Fourier Transform Infrared Spectroscopy (FT-IR), 13C nuclear magnetic resonance (13C-NMR) spectroscopy, and thermal gravimetric analysis (TGA). All the results confirmed the successful incorporation of SMAA chains into the crosslinking network of the UF resins. The modified UF resins were further employed as wood adhesives and the effect of synthesis parameters on their performance was investigated. Meanwhile, the influence of SMAA molecular weight (MW) on the properties of the modified UF resins was also studied. When the UF resins were synthesized with a low molar ratio of formaldehyde/urea (F/U) and a predetermined amount of SMAA added into the reaction system at the second step, plywood bonded using these modified UF resins showed much improved bonding strength (BS) and depressed formaldehyde emission. Moreover, the as-modified UF resins showed good storage characteristics.