The influence of selected bivalent metal ions on the photolysis of diethylenetriamine penta(methylenephosphonic acid).

Abstract:

:DTPMP is predominantly utilized as scale inhibitor. We investigated the reaction rates and degradation mechanism of DTPMP with and without addition of Fe2+, Mg2+ and Ca2+ by performing LC/MS and 31P NMR analyses. DTPMP undergoes conversion with and without addition of bivalent metal ions. The initial cleavage of DTPMP is initiated at the CN bond leading to release of IDMP as its major breakdown product. The release of smaller quantities of EABMP and AMPA confirmed the nucleophilic attack on the DTPMP amines. Oxidation of Fe2+ to Fe3+ during the initial 30 min indicated an intramolecular electron transfer changing the electron density distribution at the nitrogen centre, which increased the radical attack during UV irradiation. Independent of the fact that Fe2+ acted as catalyst and Mg2+ and Ca2+ acted as reactants, we found no significant differences in their degradation mechanisms. However, the reaction rates were strongly affected by the addition of the bivalent metal ions as Fe2+ accelerated most DTPMP degradation followed by Mg2+ and Ca2+. The UV treatment without metal ion addition was four times slower compared with Fe2+ addition. We conclude that in environments rich in ferrous iron and/or at reduced redox potential, photolysis of DTPMP will be catalysed by iron and will lead to accumulation of IDMP, EABMP and AMPA and several other none-quantifiable breakdown products.

journal_name

Chemosphere

journal_title

Chemosphere

authors

Kuhn R,Jensch R,Bryant IM,Fischer T,Liebsch S,Martienssen M

doi

10.1016/j.chemosphere.2018.07.033

subject

Has Abstract

pub_date

2018-11-01 00:00:00

pages

726-733

eissn

0045-6535

issn

1879-1298

pii

S0045-6535(18)31291-8

journal_volume

210

pub_type

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