Polyethylene terephthalate (PET),
a chemically stable polyester
with multiple applications, has risen dramatically in manufacturing
and consumption in the past decades. The increase in PET use has resulted
in considerable volumes of waste PET pilling up and thus causing increased
health and environmental concerns. Apart from the landfills and incineration
solutions, the common waste PET recycling practices mainly focus on
low-value downstream products. All the abovementioned factors have
contributed to the lower waste PET recycling overall rate of less
than 30% in South Africa and created a need for alternative treatment
options. Our earlier work has proven the feasibility for converting
clear PET bottles into high value-added metal–organic frameworks
(MOFs) materials. The feedback from industries indicated that the
colorful PET bottles and food trays are currently considered problematic
to be recycled economically. In response, this work focuses on the
use of various types of PET wastes as sources of benzene dicarboxylic
acid (BDC) linker for the synthesis of the zirconium-based MOF UiO-66(Zr).
The BDC linker was extracted from food trays, green bottles, brown
bottles, and PETCO beads through glycolysis (depolymerization). Post-synthesis
characterization revealed that textural properties of the waste PET-derived
UiO-66(Zr) MOFs were comparable to those of the MOFs derived from
commercial chemicals as exemplified in the scanning electron microscope
images and X-ray diffraction patterns. The diffraction pattern peaks
typically observed for commercial grade BDC positioned at 2θ
= 17.21, 25.01, and 27.64° were observed for the PET-derived
BDC samples, confirming the crystalline nature of samples. However,
the MOFs synthesized from BDC derived from green and brown PET bottles
measured lower Brunauer–Emmett–Teller surface areas
in the range of 933–1085 m2/g compared to 1368 m2/g for MOFs synthesized from the commercial BDC linker. This
phenomenon is attributed to the presence of organic dyes contained
in the colored PET bottles residing in the MOF pores. This was further
confirmed by the infrared spectra of the postconsumer PET-derived
BDC showing a peak at 3158 cm–1 assigned to the
amine N–H functional group, as well as the much stronger C–H
bend. This study complements the business case development model of
“waste PET to value-added MOFs”.