In
this study, novel hexagonal K2W4O13 (h-K2W4O13) nanowires were
strategically synthesized via a facial hydrothermal method, which
exhibited excellent adsorption capacities for wastewater treatment.
The inorganic agent K2SO4 was used as a structure-directing
agent to scaffold the tunnel structure of h-K2W4O13 and form the one-dimensional structure. Through increasing
the relative molar ratio of K2SO4 to Na2WO4 precursor, the pure-phase h-WO3 nanorods
and h-K2W4O13 nanowires were obtained,
attributing to the competitive electrostatic adsorption between K+ ions and Na+ ions on h-WO3 nuclei.
With a smaller hydrated radius in the solution (d
K+ = 3.31 Å, d
Na+= 3.58
Å), K+ exhibited superior affinity compared to Na+ with the negatively charged h-WO3 nuclei because
of a larger charge density, resulting in the formation of h-K2W4O13. Adsorption experimental results
showed that 89.4% of methylene blue was removed by h-K2W4O13 in the first 5 min (99% in 1 h) and the
maximum uptake capacity reached 204.08 mg g–1. In
addition, the novel h-K2W4O13 exhibited
acid or alkali resistance and good reusability, revealed by the stable
adsorption capacity in a wide pH range of 3.0–11.0 and five-run
recycle tests. The large specific area, high proportion of effective
pore volume, and abundant hydroxyl groups of the synthesized h-K2W4O13 resulted in excellent adsorption
performance for methylene blue.