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Reversible, Selective Trapping of Perchlorate from Water in Record Capacity by a Cationic Metal–Organic Framework
journal contribution
posted on 2016-01-14, 00:00 authored by Ian R. Colinas, Rachel
C. Silva, Scott R. J. OliverWe
report the capture of ppm-level aqueous perchlorate in record
capacity and kinetics via the complete anion exchange of a cationic
metal–organic framework. Ambient conditions were used for both
the synthesis of silver 4,4′-bipyridine nitrate (SBN) and the
exchange, forming silver 4,4′-bipyridine perchlorate (SBP).
The exchange was complete within 90 min, and the capacity was 354
mg/g, representing 99% removal. These values are greater than current
anion exchangers such as the resins Amberlite IRA-400 (249 mg/g),
Purolite A530E (104 mg/g), and layered double hydroxides (28 mg/g).
Moreover, unlike resins and layered double hydroxides, SBN is fully
reusable and displays 96% regeneration to SBN in nitrate solution,
with new crystal formation allowing the indefinite cycling for perchlorate.
We show seven cycles as proof of concept. Perchlorate contamination
of water represents a serious health threat because it is a thyroid
endocrine disruptor. This noncomplexing anionic pollutant is significantly
mobile and environmentally persistent. Removal of other anionic pollutants
from water such as chromate, pertechnetate, or arsenate may be possible
by this methodology.