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Boric acid catalysed hydrolysis of peroxyacids
1Faculty of Engineering and Environment, Northumbria University Newcastle upon Tyne NE1 8ST UK michael.deary@northumbria.ac.uk.
Boric acid significantly accelerates peroxyacid hydrolysis, increasing rates by 12-fold for peracetic acid (PAA) and 3-chloroperbenzoic acid (MCPBA). This catalytic effect is crucial for understanding the stability and applications of these widely used oxidizing agents.
Area of Science:
- Chemical Kinetics
- Catalysis
- Oxidative Chemistry
Background:
- Peroxyacids like peracetic acid (PAA) and 3-chloroperbenzoic acid (MCPBA) are vital in oxidation, bleaching, and disinfection.
- Understanding the hydrolysis mechanisms of peroxyacids is essential due to their widespread industrial and laboratory applications.
- Previous studies have not fully elucidated the catalytic pathways influencing peroxyacid decomposition rates.
Purpose of the Study:
- To investigate the catalytic effect of boric acid on the hydrolysis of peroxyacids.
- To determine the optimal pH conditions for boric acid-catalyzed peroxyacid hydrolysis.
- To elucidate the catalytic mechanism involving boric acid species.
Main Methods:
- Hydrolysis rates of PAA and MCPBA were measured in the presence of boric acid.
- Hydrogen peroxide formation was quantified using a specific Ti(iv) complexation method.
- Reactions were conducted across a wide pH range (3-13), with metal ion chelation using EDTA and EDTMP.
Main Results:
- Boric acid increased peroxyacid hydrolysis rates approximately 12-fold.
- Maximum hydrolysis rates were observed at pH 9 for PAA and pH 8.4 for MCPBA.
- Catalysis involves boric acid acting as a Lewis acid, with contributions from single molecules, pairs, or polyborate species.
Conclusions:
- Boric acid effectively catalyzes peroxyacid hydrolysis, impacting their stability and application.
- The catalytic mechanism is complex, involving multiple boric acid species.
- This finding provides critical insights into the chemical behavior of peroxyacids in various environments.
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