Preparation, characterization and mechanical properties of bio-based polyurethane adhesives from Isocyanate-functionalized cellulose acetate and castor oil for bonding wood
Loading...
Publication date
Advisors
Research group
Center
Abstract
Nowadays, different types of natural carbohydrates such as sugars, starch, cellulose and
their derivatives are widely used as renewable raw materials. Vegetable oils are also considered as
promising raw materials to be used in the synthesis of high quality products in different
applications, including in the adhesive field. According to this, several bio-based formulations with
adhesion properties were synthesized first by inducing the functionalization of cellulose acetate
with 1,6-hexamethylene diisocyanate and then mixing the resulting biopolymer with a variable
amount of castor oil, from 20% to 70% (wt). These bio-based adhesives were mechanically
characterized by means of small-amplitude oscillatory torsion measurements, at different
temperatures, and standardized tests to evaluate tension loading (ASTM-D906) and peel strength
(ASTM-D903). In addition, thermal properties and stability of the synthesized bio-polyurethane
formulations were also analyzed through differential scanning calorimetry and thermal
gravimetric analysis. As a result, the performance of these bio-polyurethane products as wood
adhesives were compared and analyzed. Bio-polyurethane formulations exhibited a simple
thermo-rheological behavior below a critical temperature of around 80–100 °C depending on the
castor oil/cellulose acetate weight ratio. Formulation with medium castor oil/biopolymer weight
ratio (50:50 % wt) showed the most suitable mechanical properties and adhesion performance for
bonding wood.
Unesco Subjects
Bibliographic citation
Tenorio Alfonso, A., Sánchez Carrillo, M.C., Franco Gómez, J.M.: "Preparation, characterization and mechanical properties of bio-based polyurethane adhesives from Isocyanate-functionalized cellulose acetate and castor oil for bonding wood". Polymers. Vol. 9, n. 4, (2017). DOI: 10.3390/polym9040132














