Date of Award

Summer 7-31-2024

Document Type

Thesis

Degree Name

Master of Science (MS)

Department

Chemistry

First Advisor

Dr. Ram K. Gupta

Second Advisor

Dr. Khamis Siam

Third Advisor

Dr. Timothy Dawsey

Abstract

Adhesives are important for binding diverse materials, promoting structural integrity and functional versatility in countless daily life applications. An enormous obstacle remains in the development of polyurethane (PU) adhesives exhibiting excellent bonding strength. Designing a chain extender with appropriate molecular structures is critical to improving the bonding strength of PU-based adhesives. In this work, PU-based adhesive was prepared using castor-oil-based polyol (COP) and diisocyanate. The bonding strength of the adhesive was improved by adding chain extenders such as N, N-bis(2-hydroxyethyl) thiophene-2,5-dicarboxamide (ETP) and N, N-Bis(2-hydroxyethyl)-terephthalamide (ETAM). The modified adhesive showed high bonding strength after the addition of chain extenders due to the presence of the dicarboxamide group, which served as a center for hydrogen bonding. The bonding strength of PU adhesive increased to 7.22 and 9.68 MPa from 5.0 MPa after the addition of 7.5 wt.% of ETP and 5.0 wt.% of ETAM, respectively. The bonding strength of the adhesives was tested on both wood (oak) and metal (stainless steel) coupons. The bonding strength of 9.68 MPa on oak wood and 6.73 MPa on stainless steel coupon was observed for the 5.0 wt.% of ETAM-based PU adhesive. The bonding failure was observed to be due to wood failure. The reason behind the good bonding is noncovalent bonds which are formed between the functional group of the PU molecular chain and the surface of the substrate. In addition, no major changes in Fourier transform infrared (FT-IR) spectroscopy after keeping these adhesives in different solvents were observed. Good crosslinking is also confirmed by studying the gelling and swelling data of the adhesives.

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