Preparation and characterization of Lignin-graft-poly (ɛ-caprolactone) copolymers based on lignocellulosic butanol residue.

In this paper, a "graft from" Ring-Opening Polymerization (ROP) technique was used to synthesize a lignin-graft-poly (ɛ-caprolactone) copolymer (BBL-g-PCL) using biobutanol lignin (BBL) as raw material recovered from lignocellulosic butanol residue. Polymerizations were carried out with various mass ratios of BBL and CL monomer ([BBL]/([BBL]+[CL])=1.0%, 5.0%, 10%, 20% and 40% (w/w)) to obtain BBL-g-PCL copolymers with different molecular weights, ranging from 367 to 8163gmol(-1). The grafting efficiency was preliminary evidenced by the long-term stability of dissolution of BBL-g-PCL in toluene. FT-IR and NMR analysis provided the further evidences for successful formation of BBL-g-PCL copolymer. The thermal properties of BBL-g-PCL copolymers were characterized by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). These results indicated that BBL-g-PCL copolymer had relatively good thermal stability. The static contact angle of BBL-g-PCL coating film reached to 80°. The surface functional groups and chemical composition of BBL-g-PCL copolymer was investigated in detail by X-ray photoelectron spectroscopy (XPS). The surface morphology of BBL-g-PCL copolymer was studied by Atomic force microscopy (AFM). Additionally, BBL-g-PCL coating film exhibited high absorption in the ultraviolet (UV) range, which could allow for applications in UV-blocking coatings, as well as the extents for the utilization of lignocellulosic butanol residue.