Related Experiment Video
Updated: Jun 16, 2026

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyl(tropone)iron
Published on: August 12, 2019
Reaction of decabrominated diphenyl ether by zerovalent iron nanoparticles
1Department Soil and Environmental Sciences, National Chung Hsing University, Taichung, Taiwan. yhs@nchu.edu.tw
Abstract:
Polybrominated diphenyl ethers (PBDEs) recognized as a new class of environmental persistent toxic contaminants have been distributed widely in the world. In this study, the synthesized nanoscale zerovalent iron (NZVI) in the laboratory was used to investigate the removal kinetics and mechanisms of decabrominated diphenyl ether (DBDE) at different pH. Within 40 min 90% of DBDE was rapidly removed by NZVI as compared to around 40 d needed for 24-fold weight of microscale ZVI. The removal by NZVI is much faster than that by microscale ZVI due to its high surface area and reactivity. At a different pH, the pseudo-first-order removal rate constants of DBDE linearly increased from 0.016 to 0.024 min(-1) with the decreasing of aqueous initial pH values from 10 to 5. The degradation of DBDE with NZVI is favorable in an acid condition. The debromination pathways of DBDE with NZVI were proposed on the basis of the identified reaction intermediates ranging from nona- to mono-brominated diphenyl ethers (BDEs) for an acid condition and from nona- to penta-BDEs for an alkaline condition. The debromination of PBDEs from para positions is more difficult than that from meta or ortho positions. Adsorption on NZVI also plays a role on the removal of DBDE. These findings can facilitate the treatment and fate prediction of PBDEs with NZVI in the environment.
More Related Videos
08:13Microwave-driven Synthesis of Iron Oxide Nanoparticles for Fast Detection of Atherosclerosis
Published on: March 22, 2016
15:03Synthesis of Functionalized Magnetic Nanoparticles, Their Conjugation with the Siderophore Feroxamine and its Evaluation for Bacteria Detection
Published on: June 16, 2020
Related Concept Videos
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene
Structure of Benzene: Kekulé Model
He proposed that benzene has a cyclic structure of six carbon atoms attached to one hydrogen atom each, with three alternating pi bonds.
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
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 reactions,...
Hydrolysis of Chlorobenzene to Phenol: Dow Process