Citation: Bisneto, M.P.d.S.; Gouveia,
J.R.; Antonino, L.D.; Tavares, L.B.; Ito,
N.M.; dos Santos, D.J. Effects of
Functionalized Kraft Lignin
Incorporation on Polypropylene
Surface Energy and Practical
Adhesion. Polymers 2022, 14, 999.
https://doi.org/10.3390/
polym14050999
Academic Editors: John Vakros,
Evroula Hapeshi, Catia Cannilla and
Giuseppe Bonura
Received: 17 January 2022
Accepted: 27 February 2022
Published: 1 March 2022
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polymers
Article
Effects of Functionalized Kraft Lignin Incorporation on
Polypropylene Surface Energy and Practical Adhesion
Manuel Patricio da Silva Bisneto
1
, Julia Rocha Gouveia
1
, Leonardo Dalseno Antonino
1
, Lara Basílio Tavares
1
,
Nathalie Minako Ito
1
and Demetrio Jackson dos Santos
1,2,
*
1
Nanoscience and Advanced Materials Graduate Program (PPG-Nano), Federal University of ABC (UFABC),
Santo Andre 09210-580, Brazil; manuel.bisneto@ufabc.edu.br (M.P.d.S.B.); juliargouveia@gmail.com (J.R.G.);
leonardoantonino@hotmail.com (L.D.A.); lara.btavares@hotmail.com (L.B.T.);
nathalie.minako@gmail.com (N.M.I.)
2
Center of Engineering, Modeling and Applied Social Sciences, Federal University of ABC (UFABC),
Santo Andre 09210-580, Brazil
* Correspondence: demetrio.santos@ufabc.edu.br
Abstract: Polypropylene (PP) is a multifunctional and widely applied polymer. Nevertheless, its low
energy surface and poor adhesion are well-known and might impair some prospective applications.
Aiming to overcome these limitations, PP composites can be applied as a tool to enhance PP surface
energy and then increase its practical adhesion. In this work, Kraft lignin (KL) was chemically
modified and blended with PP. In short, KL was hydroxypropylated and further reacted with
acetic anhydride (A-oxi-KL) or maleic anhydride (M-oxi-KL). Lignin modifications were confirmed
by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and
thermogravimetric analysis (TGA). PP-composites with different lignin contents, as well as pristine
PP, were characterized in terms of their thermal behavior, morphology, surface energy, and practical
adhesion by DSC, scanning electron microscopy (SEM), contact angle measurement, and peeling
tests, respectively. Lignin incorporation did not affect the PP degree of crystallization. The lignin
modifications led to a better compatibility with the PP matrix and surface energies up to 86% higher
than neat PP. Increases of up to 66% in the peel strength were verified. Composites with M-oxi-
KL showed the best adhesion performance, confirming the lignin functionalization is an efficient
approach to improve the practical adhesion of PP films.
Keywords: lignin; surface energy; wettability; practical adhesion
1. Introduction
Polypropylene (PP) is a multifunctional and low-cost polymer widely used in indus-
trial applications. Nevertheless, it presents low surface energy because of its non-polar
chemically stable structure, which leads to adhesion hindrance, such as coating failures
or flexible laminated layers delamination. Polymer blending can be used as a strategy to
alter the wettability of PP and increase the strength of PP adhesive joints. The combination
of PP with renewable resource materials has been intensively investigated as a promising
approach to reduce petroleum-based dependency, hence collaborating to a reduced environ-
mental impact. The wettability and surface roughness of polypropylene can be improved
when filled with wood flour [1]. Cellulose, potato starch, and chitosan were also reacted
with PP for membranes application, and the new materials changed their hydrophobicity,
besides mechanical properties improvements [2].
Another strategy arises from a remarkable sustainable raw material that has been
successfully applied as high-added-value for polymer blends and composites. Lignin, the
second most abundant biopolymer on earth, can be found in all vascular plants and is an
amorphous phenolic polymer, consisting of three main phenylpropane units (guaiacyl, syn-
rigyl, and p-hidroxyphenyl) [3], that must be isolated from the other components, cellulose
Polymers 2022, 14, 999. https://doi.org/10.3390/polym14050999 https://www.mdpi.com/journal/polymers