Removal of Malachite Green Dye using Keggin Polyoxometalate Intercalated ZnAl Layered Double Hydroxide

The ZnAl Layered double hydroxides (LDHs) have been successfully synthesized by the coprecipitation method, followed by intercalation using Keggin ion of α-dodecatungstosilicic acid [α-SiW12O40]4- to form ZnAl-[α-SiW12O40] LDHs. The prepared ZnAl-[SiW12O40] LDHs were characterized by using X-Ray, FTIR, and BET surface area analyses, which were, then, used as adsorbents of malachite green dye from aqueous solution. The synthesized ZnAl LDH showed a typical diffraction peak of the layered compound at 11o (003) with an interlayer space of 8.59 Å. After intercalation, it was recorded that the interlayer space of ZnAl-[SiW12O40] LDH increased to 10.65 Å. Moreover, the specific surface area of the intercalated LDH increased from 1.9685 to 14.0422 Å. The adsorption study revealed that the adsorption capacity of ZnAl-[SiW12O40] LDH toward malachite green dye was higher (37.514 mg.g-1) than the pristine ZnAl LDH (32.845 mg.g-1). The adsorption kinetics study showed that malachite green adsorption onto both pristine and intercalate LDH followed the pseudo-2nd-order model. The adsorption thermodynamic investigation indicated that adsorption of malachite green onto ZnAl-[SiW12O40] LDH was a spontaneous process and was classified as physical adsorption with activation energy ranging from 10.074 to 15.476 kJ.mol-1. HIGHLIGHTS ZnAl LDH intercalated by Keggin ion has been successfully synthesized by facile coprecipitation followed by ion exchange method The basal spacing of the intercalated ZnAl LDH increased up to 10.65 A The intercalated ZnAl LDH exhibited higher adsorption capacity for malachite green dye removal compared with the original ZnAl LDH

Synthesis, structure and stability of three V-substituted polyoxoniobate clusters based on [TeNb9O33]17- units

Three structurally intriguing polyoxoniobates (PONbs) based on the trivacant B-type α-Keggin ion {TeNb9O33}, H4K(CN3H6)2{[Cu4(2,2’-bipy)4(H2O)2][TeNb9V2O37]}·29H2O (1, 2,2’-bipy = 2,2'-bipyridine), H0.5K5Na2.5{[Cu(en)H2O]3[TeNb9V3O39]}·10H2O (2, en = ethylenediamine), and K3Na5{[Cu(1,3-dap)H2O]3[TeNb9V3O39]}·11H2O (3, 1,3-dap = 1,3-diaminopropane) are...

Removal of Iron(II) Using Ni/Al Layered Double Hydroxide Intercalated with Keggin Ion

Layered double hydroxide (LDH) Ni/Al-NO3 was synthesized using a coprecipitation method under base condition following with intercalation using Keggin ion [a-SiW12O40]4- to form Ni/Al-[a-SiW12O40] LDH. The LDHs were characterized using XRD, FTIR, BET, and pHpzc analyses. Furthermore, LDHs were applied as adsorbent of iron(II) from aqueous solution. The adsorption process was studied through the effect of adsorption time, the concentration of iron(II), and temperature adsorption. The results show the interlayer distance of LDHs was increased from 7.408 Å to 10.533 Å after intercalation process. The adsorption of iron(II) on LDHs showed that adsorption of iron(II) on both LDHs follows pseudo first-order kinetic model with R2 value is close to one. The adsorption process was spontaneous, with adsorption capacity up to 36.496 mg g-1.

Spontaneous formation of autocatalytic sets with self-replicating inorganic metal oxide clusters

Here we show how a simple inorganic salt can spontaneously form autocatalytic sets of replicating inorganic molecules that work via molecular recognition based on the {PMo12} ≡ [PMo12O40]3– Keggin ion, and {Mo36} ≡ [H3Mo57M6(NO)6O183(H2O)18]22– cluster. These small clusters are able to catalyze their own formation via an autocatalytic network, which subsequently template the assembly of gigantic molybdenum-blue wheel {Mo154} ≡ [Mo154O462H14(H2O)70]14–, {Mo132} ≡ [MoVI72MoV60O372(CH3COO)30(H2O)72]42– ball-shaped species containing 154 and 132 molybdenum atoms, and a {PMo12}⊂{Mo124Ce4} ≡ [H16MoVI100MoV24Ce4O376(H2O)56 (PMoVI10MoV2O40)(C6H12N2O4S2)4]5– nanostructure. Kinetic investigations revealed key traits of autocatalytic systems including molecular recognition and kinetic saturation. A stochastic model confirms the presence of an autocatalytic network involving molecular recognition and assembly processes, where the larger clusters are the only products stabilized by the cycle, isolated due to a critical transition in the network.

Energetics of paramagnetic oxide clusters: the Fe(iii) oxyhydroxy Keggin ion

The full energy landscape of the iron(iii) oxyhydroxy Keggin ion is explored through a combination of computation and predictive fitting.

Adsorption of Cadmium(II) Using Ca/Al Layered Double Hydroxides Intercalated with Keggin Ion

Ca/Al layered double hydroxides (Ca/Al LDH) was synthesized using co-precipitation method following calcination at 800 °C and was intercalated with Keggin ion [α-SiW12O40]4– to form intercalated Ca/Al LDH. Materials were characterized using XRD and FTIR spectrophotometer. Furthermore, materials were used as an adsorbent of cadmium(II) from solution. The results showed that layer material was formed completely after calcination which was indicated at diffraction 20° due to loss of water in the interlayer space. Ca/Al LDH after calcination was intercalated with [α-SiW12O40]4– ion and interlayer distance was increased from 4.25 to 4.41 Å showed that intercalation process was successfully conducted. Adsorption of cadmium(II) using Ca/Al LDH was conducted at pH 9 and intercalated Ca/Al LDH at pH 8 showed that intercalated material has slightly faster than Ca/Al LDH without intercalation probably due to slightly increasing interlayer distance of Ca/Al LDH after intercalation. The adsorption capacity of intercalated Ca/Al LDH was higher than Ca/Al LDH without intercalation at the temperature range of 30–50 °C.