Chitosan-Transition Metal Coordination Biopolymer: A Promising Heterogeneous Catalyst for Radical Ion Polymerization of Vinyl Acetate at Ambient Temperature.

29 March 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The present study utilized chitosan obtained from crab shell and transition metal salts as precursors to synthesize chitosan-metal coordination biopolymers of Mn(II), Fe(III), Co(II) and Ni(II) [i.e Chit-Mn(II), Chit-Fe(III), Chit-Co(II) and Chit-NI(II) respectively]. The synthesized coordination biopolymers have been characterized using different instrumental techniques such as spectroscopic (UV-visible, FT-IR, XRD, EDS, and ICP-OES), thermal analysis (TGA and DTA), surface analysis (SEM), and hydrogen-temperature programmed reduction (H2-TPR) analysis. Spectroscopic studies confirmed the successful incorporation of the metals into the biopolymer matrix. Thermal analysis and H2-TPR revealed the reducibility of the Chit-Fe(III) at 120 ℃. While Chit-Fe(III) and Chit-Ni(II) were inactive, Chit-Co(II) and Chit-Mn(II) were found to be active towards vinyl acetate polymerization in the presence of aqueous Na2SO3. Furthermore, the polyvinyl acetate (PVAc) produced from Chit-Co(II) compared perfectly with a commercial PVAc and was in higher yield than PVAc produced from Chit-Mn(II). The polymerization has been shown to proceed via surface-initiated atom transfer radical polymerization (SI-ATRP), and the viscosity average molecular weight of PVAc produced has been measured as 25, 078. The density functional theory approach has been used to ascertain the coordination orientation of the Chit-Co(II) and explain its high efficiency towards vinyl acetate polymerization. The catalyst reusability test revealed an insignificant loss of activity for the Chit-Co(II) after seven cycles of polymerization. Kinetic studies show that the vinyl acetate polymerization suits the second-order kinetic model at ambient temperature. Thermodynamic studies also revealed that chain initiation is an endothermic process while chain propagation is an exothermic process. The result of this work also suggests an investigation of chitosan-metal coordination biopolymer via low-ppm ATRP approach for possible biomedical application.

Keywords

Chitosan-metal coordination biopolymer
Polyvinyl acetate
Viscosity average molecular weight
density functional theory
Surface-initiated atom transfer radical polymerization

Supplementary materials

Title
Description
Actions
Title
Graphical absract2 p2
Description
Actions
Title
Supplementary Information JPR
Description
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.