# Water‐Soluble Iron Porphyrins as Catalysts for Suppressing Chlorinated Disinfection Byproducts in Hypochlorite‐Dependent Water Remediation

**Authors:** Silène Engbers, Maja J. Lind, Mathias L. Skavenborg, Johannes E. M. N. Klein, Frants R. Lauritsen, Christine J. McKenzie

PMC · DOI: 10.1002/cssc.202402171 · 2025-01-10

## TL;DR

Scientists found that iron porphyrins can help reduce harmful byproducts in water treatment while still effectively cleaning the water.

## Contribution

The study introduces water-soluble iron porphyrins as effective catalysts for suppressing chlorinated byproducts during water remediation.

## Key findings

- Both positively and negatively charged iron porphyrins equally suppress chlorinated disinfection byproducts.
- Spectroscopic studies revealed transient formation of Compound II and regeneration of iron(III) porphyrin at low hypochlorite concentrations.
- Iron porphyrins promote phenol degradation to CO2 and H2O without forming harmful byproducts.

## Abstract

We are facing a world‐wide shortage of clean drinking water which will only be further exacerbated by climate change. The development of reliable and affordable methods for water remediation is thus of utmost importance. Chlorine (which forms active hypochlorites in solution) is the most commonly used disinfectant due to its reliability and low cost. One drawback is that it reacts with organic pollutants to generate toxic chlorinated byproducts. To mitigate chlorination in water remediation, we have investigated the use of catalytic amounts of charged water‐soluble iron porphyrins. These are known to activate hypochlorite to generate high valent oxoiron species. We studied the depletion of the model micropollutant phenol and the accumulation of chlorinated disinfection byproducts under water remediation conditions, using iron porphyrins [(TMPyP)FeCl]Cl4 and (NH4)4[(TPPS)FeCl] as catalysts, by membrane inlet mass spectrometry. Despite bearing opposite charges on the meso‐substituent, both iron porphyrins suppress the formation of chlorinated disinfection by‐products equally well. To gain further insight, spectroscopic studies were performed. These showed the transient formation of Compound II, followed by either regeneration of the iron(III) porphyrin at low NaOCl concentrations, or total decomposition of the porphyrin complex at high NaOCl concentrations. Potential future directions for modifications of porphyrin‐based catalysts are discussed.

Water remediation using chlorine (for which hypochlorite is the active disinfectant) has the disadvantage of degrading micropollutants to chlorinated compounds. To bypass this and promote total mineralization of the model micropollutant phenol to CO2 and H2O, we investigated the use of catalytic amounts of iron porphyrins in hypochlorite‐dependent water remediation. Porphyrins bearing positive and negative charges on the meso‐substituent are both active for the suppression of accumulation of chlorinated byproducts, without hindering the degradation of phenol.

## Linked entities

- **Chemicals:** chlorine (PubChem CID 312), hypochlorite (PubChem CID 61739), phenol (PubChem CID 996), CO2 (PubChem CID 280), H2O (PubChem CID 962)

## Full-text entities

- **Chemicals:** porphyrin (MESH:D011166), Hypochlorite (MESH:D006997), drinking water (MESH:D060766), NaOCl (MESH:D012973), Chlorine (MESH:D002713), (NH4)4 (-), Water (MESH:D014867), phenol (MESH:D019800)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12051255/full.md

---
Source: https://tomesphere.com/paper/PMC12051255