Although lignin is currently an under-utilized biopolymer, it has the potential to be valorized through different modification pathways to yield alternative products to petroleum-based ones. In this work, hydrolysis lignin (HL) was copolymerized with acrylamide (AM) and acrylic acid (AA) under acidic conditions to generate the lignin/AM polymer (HM), lignin/AA polymer (HA), and lignin/AM/AA copolymer (HAM) with different negative charge densities and molecular weights. Lignin-based polymers characterized by advanced tools, such as proton nuclear magnetic resonance (1H NMR), gel permission chromatography (GPC), and elemental analysis confirmed the successful polymerization of HL with AM, AA, or AM/AA monomers. The adsorption analysis using a quartz crystal microbalance (QCM) revealed that compared to diblock HM and HA, the triblock copolymers of HAM adsorbed more on the Al2O3 surface and generated a bulkier adsorbed layer, which is important for lignin-based coating formulation. HAM1 with a lower charge density yielded a higher surface excess density, while HAM2 with a larger R h occupied more space (153.7 Å2) at the interface of water and Al2O3. In suspension systems, because of the higher M w, R h, and adsorption affinity, the bridging performance of HAM2 was more remarkable than that of the other lignin derivatives for Al2O3 particles via forming stronger flocs (with a deflocculation parameter, T df, of 80.6 s). However, the diblock lignin-AA (HA1) polymer showed the fastest floc regrowth capability after reducing the shear forces (with a reflocculation parameter, T rf, of 62.5 s). The high thermal stability, T g, and rheological characteristics of the HAM copolymer proved that it can be an excellent material for coating formulations and flocculants for wastewater treatment systems.
© 2021 The Authors. Published by American Chemical Society.