Synthesis and characterization of cellulose acetate from TCF oil palm empty fruit bunch pulp

Closed

Fauzi Muhammad Djuned, Mohammad Asad, Mohamad Nasir Mohamad Ibrahim, Wan Rosli Wan Daud

2014 BioResources Vol. 9 Issue 3 Article Cited by 32 SDG 12SDG 17 Quartile

Abstract

Cellulose acetate (CA) was successfully synthesized by the acetylation of TCF cellulose pulp from oil palm empty fruit bunches (OPEFB) at room temperature, using acetic anhydride as the acetylating agent and acetic acid as the solvent in the presence of sulfuric acid/sodium bisulfate as catalysts. Degree of substitution (DS) was controlled by the variables of acetylation time and acetic anhydride to cellulose ratio, under the heterogeneous state. The product (CA) obtained was characterized through Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance spectroscopy (NMR), differential scanning calorimetry (DSC), X-ray diffraction (XRD), and scanning electron microscopy (SEM). The results indicate that the CA obtained has characteristics similar to commercial CA, and DS is significantly dependent on acetylation time and the acetic anhydride-to-cellulose ratio. © 2014 North Carolina State University.

Affiliations

Bioresource, Paper and Coating Technology Division, School of Industrial Technology, Universiti Sains Malaysia, Minden, Penang, 11800, Malaysia; Chemical Engineering Department, Universitas Syiah Kuala, Jl. Syech Abdurrauf Kopelma Darussalam, Banda Aceh, Indonesia; School of Chemical Sciences, Universiti Sains Malaysia, Minden, Penang, 11800, Malaysia

Research at a Glance

Premium content — register to unlock

Research at a Glance

Register to unlock

Topics & SDG Alignment

Premium content — register to unlock

Topics & SDG Alignment

Register to unlock

Collaboration

Premium content — register to unlock

Collaboration

Register to unlock

Author Profile (Selected)

Premium content — register to unlock

Author Profile (Selected)

Register to unlock

References Overview

Premium content — register to unlock

References Overview

Register to unlock

Journal & Source

Premium content — register to unlock

Journal & Source

Register to unlock

Metadata & Integrity

Premium content — register to unlock

Metadata & Integrity

Register to unlock