Related Experiment Video
Updated: May 28, 2025

Author Spotlight: A New and Efficient Method for Comprehensive Metabolite Cytotoxicity Assessment of Triazole Pesticides in Plants
Published on: December 22, 2023
Interaction between Tetrabromobisphenol A and invertebrates in rigid polyurethane biodegradation: Inhibitory effects,
Ping Zhu1, Teng Xie1, Shuangshuang Gong1
1School of Environmental and Chemical Engineering, Shanghai University, 99 Shangda Road, Shanghai 200444, People's Republic of China.
Abstract:
Tetrabromobisphenol A (TBBPA) is a brominated flame retardant widely used in electronic plastics, but its effects on invertebrate-mediated plastic biodegradation remain unclear. This study investigated the impact of TBBPA on the biodegradation of rigid polyurethane (RPU) by Galleria mellonella and Tenebrio molitor larvae, and the effects of both larvae on the chemical transformation of TBBPA. Results showed that TBBPA inhibited the uptake of RPU by both larvae, resulting in a decrease of intestinal protein-like fluorescence intensity, reduced the concentrations of certain metabolic by-products of RPU, and inhibited the growth of RPU degradation related bacteria. Most TBBPA was excreted by both larvae, and a small fraction was transformed into less toxic brominated organic compounds. Sequencing analysis suggested that Enterobacteriaceae, Enterococcus, and non-dominant gut bacteria might play a role in TBBPA degradation. This study provides detailed insights into the interactions involved in the biodegradation of TBBPA-containing RPU by two invertebrate species.
Related Concept Videos
Types of Step-Growth Polymers: Polyesters
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the...
Polymer Classification: Architecture
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
Radical Chain-Growth Polymerization: Overview

