Abstract

Emerging water purification applications often require tunable and ion-selective technologies. For example, when treating water for direct use in irrigation, often monovalent Na+ must be removed preferentially over divalent minerals, such as Ca2+, to reduce both ionic conductivity and sodium adsorption ratio (SAR). Conventional membrane-based water treatment technologies are either largely non-selective or not dynamically tunable. Capacitive deionization (CDI) is an emerging membraneless technology that employs inexpensive and widely available activated carbon electrodes as the active element. We here show that a CDI cell leveraging sulfonated cathodes can deliver long-lasting, tunable monovalent ion selectivity. For feedwaters containing Na+ and Ca2+, our cell achieves a Na+/Ca2+ separation factor of up to 1.6. To demonstrate the cell longevity, we show that monovalent selectivity is retained over 1000 charge–discharge cycles, the highest cycle life achieved for a membraneless CDI cell with porous carbon electrodes to our knowledge, while requiring an energy consumption of ~0.38 kWh/m3 of treated water. Furthermore, we show substantial and simultaneous reductions of ionic conductivity and SAR, such as from 1.75 to 0.69 mS/cm and 19.8 to 13.3, respectively, demonstrating the potential of such a system towards single-step water treatment of brackish and wastewaters for direct use in irrigation.

Highlights

  • The problem of hazardous compounds present at low concentrations in water sources spans domains from public health to heavy industry

  • We first employ a dynamics of a complete Capacitive deionization (CDI) cell with an electrolyte containing competing smaller-sized Na+ and larger Ca2+, and includes a combined dynamic-modified Donnan (mD) model and predict that functionalized electrodes enhance monovalent selectivity at short charging times nanopore chemical charge concentration, σchem, such as that created by strong-acid groups

  • We demonstrate that sulfonated electrodes can serve as the foundation for long-lasting, monovalent selective, membraneless CDI systems, displays the P–P

Read more

Summary

Introduction

The problem of hazardous compounds present at low concentrations in water sources spans domains from public health to heavy industry. We first employ a dynamics of a complete CDI cell with an electrolyte containing competing smaller-sized Na+ and larger Ca2+, and includes a combined dynamic-mD model and predict that functionalized electrodes enhance monovalent selectivity at short charging times nanopore chemical charge concentration, σchem, such as that created by strong-acid (e.g. sulfonic) groups.

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call