RESUMO
Exposure of humans to Arsenic from groundwater drinking sources is an acute global public health problem, entailing the urgent need for highly efficient/low-cost Arsenite (AsIII) up-taking materials. Herein we present an innovative hybrid-material, ZrMOF@SFd operating like an "AsIII-sponge" with unprecedented efficiency of 1800 mg AsIII gr-1. ZrMOF@SFd consists of a neutral Zirconium Metal-Organic Framework [ZrMOF] covalently grafted on a natural silk-fiber (SFd). ZrMOF itself exhibits AsIII adsorption of 2200 mg gr-1, which supersedes any -so far- known AsΙΙΙ-sorbent. Using XPS, FTIR, BET-porosimetry data, together with theoretical Surface-Complexation-Modeling (SCM), we show that the high-AsΙΙΙ-uptake is due to a sequence of two phenomena:[i] at low AsIII-concentrations, surface-complexation of H3AsO3 results in AsIII-coated voids of ZrMOF, [ii] at increased AsIII-concentrations, the AsIII-coated voids of ZrMOF are filled-up by H3AsO3 via a partitioning-like mechanism. In a more general context, the present research exemplifies a mind-changing concept, i.e. that a "partitioning-like" mechanism can be operating for adsorption of metalloids, such as H3AsO3, by metal oxide materials. So far, such a mechanism has been conceptualized only for the uptake of non-polar organics by natural organic matter or synthetic polymers.
RESUMO
The composite anion-exchange material MOR-1-HA (metal-organic resin-1-alginic acid) was investigated as sorbent for the capture of the methyl orange anion (MO- ) from aqueous solutions. MOR-1-HA shows a remarkably high sorption capacity (up to 859â mg g-1 ) and rapid sorption kinetics, the fastest among the reported metal-organic sorbents. It is capable of absorbing MO- over a wide pH range (1-8) and, in addition, it exhibits significant MO- sorption affinity even in the presence of large excesses of competing anions (e.g., Cl- , NO3 - , SO4 2- ). The exceptional MO- -sorption properties of MOR-1-HA arise not only from its highly porous structure and easily exchangeable Cl- anions, but also from a multitude of interaction effects, such as electrostatic interactions between MO- and the NH3 + groups of the material, hydration/dehydration, hydrophobicity/hydrophilicity, size and capacity of generating lateral interactions, and intercalation as revealed by theoretical studies. An ion-exchange column with a stationary phase containing MOR-1-HA and silica sand showed high efficiency for the removal of MO- from various types of aqueous samples. The column can be readily regenerated and reused for many runs with minimal loss (2.3-9.3 %) of its exchange capacity. The simplicity of the MOR-1-HA/sand column and its high regeneration capability and reusability make it particularly attractive for application in the remediation of MO- -contaminated industrial wastewater.
RESUMO
We report an anion exchange composite material based on a protonated amine-functionalized metal-organic framework, denoted Metal Organic Resin-1 (MOR-1), and alginic acid (HA). MOR-1-HA material shows an exceptional capability to rapidly and selectively sorb Cr(vi) under a variety of conditions and in the presence of several competitive ions. The selectivity of MOR-1-HA for Cr(vi) is shown to be the result of strong O3CrVI···NH2 interactions. The composite sorbent can be successfully utilized in an ion-exchange column, in contrast to pristine MOR-1 which forms fine suspensions in water passing through the column. Remarkably, an ion exchange column with only 1% wt MOR-1-HA and 99% wt sand (an inert and inexpensive material) is capable of reducing moderate and trace Cr(vi) concentrations to well below the acceptable safety limits for water. The relatively low cost of MOR-1-HA/sand column and its high regeneration capability and reusability make it particularly attractive for application in the remediation of Cr(vi)-bearing industrial waste.
RESUMO
[This corrects the article DOI: 10.1039/C5SC03732H.].
