A State-of-the-Art of Metal-Organic Frameworks for Chromium Photoreduction vs. Photocatalytic Water Remediation.

Hexavalent chromium (Cr(VI)) is a highly mobile cancerogenic and teratogenic heavy metal ion. Among the varied technologies applied today to address chromium water pollution, photocatalysis offers a rapid reduction of Cr(VI) to the less toxic Cr(III). In contrast to classic photocatalysts, Metal-Organic frameworks (MOFs) are porous semiconductors that can couple the Cr(VI) to Cr(III) photoreduction to the chromium species immobilization. In this minireview, we wish to discuss and analyze the state-of-the-art of MOFs for Cr(VI) detoxification and contextualizing it to the most recent advances and strategies of MOFs for photocatalysis purposes. The minireview has been structured in three sections: (i) a detailed discussion of the specific experimental techniques employed to characterize MOF photocatalysts, (ii) a description and identification of the key characteristics of MOFs for Cr(VI) photoreduction, and (iii) an outlook and perspective section in order to identify future trends.

Chromium Speciation in Zirconium-Based Metal-Organic Frameworks for Environmental Remediation.

Acute CrVI water pollution due to anthropogenic activities is an increasing worldwide concern. The high toxicity and mobility of CrVI makes it necessary to develop dual adsorbent/ion-reductive materials that are able to capture CrVI and transform it efficiently into the less hazardous CrIII . An accurate description of chromium speciation at the adsorbent/ion-reductive matrix is key to assessing whether CrVI is completely reduced to CrIII , or if its incomplete transformation has led to the stabilization of highly reactive, transient CrV species within the material. With this goal in mind, a dual ultraviolet-visible and electron paramagnetic spectroscopy approach has been applied to determine the chromium speciation within zirconium-based metal-organic frameworks (MOFs). Our findings point out that the generation of defects at Zr-MOFs boosts CrVI adsorption, whilst the presence of reductive groups on the organic linkers play a key role in stabilizing it as isolated and/or clustered CrIII ions.

Synthesis and characterization of activated carbon from sawdust of Algarroba wood. 1. Physical activation and pyrolysis.

Synthesis of activated carbon (AC) from sawdust of Algarroba wood was performed as a function of the temperature under CO(2) and N(2) flow. Characterization was performed by adsorption-desorption N(2) isotherms, FTIR, XPS and SEM. Functional acid or basic groups were detected on the surface of AC. For both studied atmospheres, the maximum value of surface area was obtained at 800°C. A monotonic correlation between temperature and mean pore diameter was detected being the higher the activation temperature the lower the mean pore width of AC. Ultramicroporous AC with pore diameters of 6.7 Å and 5.3 Å were obtained at 900°C under CO(2) and N(2) flow, respectively. It can be concluded that pore diameter and the functionalization of the AC surface can be controlled easily controlling the temperature of activation, independently of the gas atmosphere. The present results suggest that waste biomass is a potential source for the synthesis of carbon materials with potential novel applications.