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March 21, 2026Water Research2 citationsOpen Access

Critical Degree of Desalination (CDD), novel parameter for optimising the removal of ammonium ion from complex matrices in electrodialysis

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IKIosif KaniadakisZYZhenqiu YangMPMarianna Papadopoulou

Key Points

  • The aim is to improve ammonium ion removal through electrodialysis by introducing the critical degree of desalination (CDD) as an operational parameter.
  • Evaluated three feed solutions mimicking different molar cation compositions of reject water.
  • Utilized both monovalent-selective cation-exchange membranes (mCEMs) and conventional cation-exchange membranes (CEMs).
  • Assessed ammonium ion removal efficiency and energy consumption across varying molar fractions.
  • mCEMs showed enhanced perm-selectivity for ammonium over divalent cations like Mg²⁺ and Ca²⁺.
  • At a low ammonium fraction (0.32), mCEMs achieved greater current efficiency than CEMs.
  • Energy consumption was lower for mCEMs at an intermediate ammonium fraction (0.58) but peaked at the critical degree of desalination (CDD).
  • At a high ammonium fraction (0.89), mCEMs had negligible benefits compared to CEMs.

Abstract

• Applying a critical degree of desalination (CDD) in electrodialysis (ED) achieves highest NH 4 + removal efficiency for the lowest energy consumption. • Monovalent CEM (mCEM) may not benefit ED for NH 4 + removal from reject waters with molar fraction around 0.89. • High concentration of K + can outcompete NH 4 + removal in ED with mCEM. • In sequence batch operation, the CDD allowed longer operation of the ED in a lower energy consumption. Complex waste streams, such as sludge reject water from anaerobic digestion, often contain a multitude of cations at varying concentrations, with the ammonium ion (NH₄⁺) typically being the most abundant. Recently, electrodialysis (ED) has been developed as a technology for the removal and recovery of NH₄⁺ from reject water. However, the further development of ED for targeting NH₄⁺ recovery faces lack of reliable performance prediction and standardized operating strategies due to cation competition. It is postulated that selective rejection of divalent cations can be achieved through the use of monovalent-selective cation-exchange membranes (mCEMs). Due to their higher electrical resistance, questions remain regarding the cationic compositions under which mCEMs provide a substantial performance benefit. In the present study, three feed solutions simulating different molar cation compositions of reject water were subjected to ED using both mCEMs and conventional cation-exchange membranes (CEMs). The feed solutions were categorized based on the molar fraction of NH₄⁺ relative to the total cation content. Results showed that the perm-selectivity of NH₄⁺ over Mg²⁺ and Ca²⁺ was enhanced when using mCEMs. Moreover, mCEMs resulted in a higher overall NH₄⁺ removal efficiency compared to standard CEMs. At a relatively low NH₄⁺ molar fraction (0.32), mCEMs outperformed CEMs in terms of current efficiency. Notably, at an intermediate molar fraction (0.58), energy consumption was lower for mCEMs compared to CEMs, but only up to a critical degree of desalination (CDD). At a high molar fraction (0.89), the contribution of mCEMs was insignificant compared to that of CEMs. The CDD was identified as a pragmatic operational parameter beyond which further desalination leads to disproportionate energy penalties. For on-site-process-control of NH 4 + removal with ED, the CDD demonstrated that membrane selection and operating thresholds are strongly dependent on reject water composition.

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Cite This Study

Kaniadakis et al. (2026) studied this question.

synapsesocial.com/papers/69be37626e48c4981c676ff8https://doi.org/10.1016/j.watres.2026.125770
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