Xitong Liu

Application potential of carbon nanotubes in water treatment: A review.

Water treatment is the key to coping with the conflict between peoples increasing demand for water and the world-wide water shortage. Owing to their unique and tunable structural, physical, and chemical properties, carbon nanotubes (CNTs) have exhibited great potentials in water treatment. This review makes an attempt to provide an overview of potential solutions to various environmental challenges by using CNTs as adsorbents, catalysts or catalyst support, membranes, and electrodes. The merits of incorporating CNT to conventional water-treatment material are emphasized, and the remaining challenges are discussed.

Enhanced Removal of Fluoride by Polystyrene Anion Exchanger Supported Hydrous Zirconium Oxide Nanoparticles

Here we fabricated a novel nanocomposite HZO-201, an encapsulated nanosized hydrous zirconium oxide (HZO) within a commercial porous polystyrene anion exchanger D201, for highly efficient defluoridation of water. HZO-201 exhibited much higher preference than activated alumina and D201 toward fluoride removal when competing anions (chloride, sulfate, nitrate, and bicarbonate) coexisted at relatively high levels. Fixed column adsorption indicated that the effective treatable volume of water with HZO-201 was about 7-14 times as much as with D201 irrespective of whether synthetic solution or groundwater was the feeding solution. In addition, HZO-201 could treat >3000 BV of the acidic effluent (around 3.5 mg F(-)/L) per run at pH 3.5, compared to only ∼4 BV with D201. The exhausted HZO-201 could be regenerated by NaOH solution for repeated use without any significant capacity loss. Such attractive performance of HZO-201 resulted from its specific hybrid structure, that is, the host anion exchanger D201 favors the preconcentration of fluoride ions inside the polymer based on the Donnan principle, and the encapsulated nanosized HZO exhibits preferable sequestration of fluoride through specific interaction, as further demonstrated by XPS spectra. The influence of solution pH, competitive anions, and contact time was also examined. The results suggested that HZO-201 has a great potential in efficient defluoridation of groundwater and acidic mine drainage.

Photodegradation of Acid Orange 7 in a UV/acetylacetone process.

Acetylacetone (AcAc) was employed as a photo-activator for the degradation of Acid Orange 7 (AO7) under UV irradiation. The feasibility of this process (named as UV/AcAc) was evaluated through comparison with the well-established UV/H2O2 process in terms of absorption spectrum and the biodegradability of the solutions. A complete decoloration of the AO7 solution could be fulfilled with AcAc at mM level. A self-acceleration phenomenon was observed for the UV/AcAc process. The pseudo first-order decoloration rate constant of AO7 in the UV/AcAc process was several times higher than that in the UV/H2O2 process, depending on the irradiation conditions. The BOD to COD ratio of the solutions increased from below 0.1 to above 0.3, along with a slight mineralization. Based on degradation product analysis, the possible pathways for AO7 degradation in the UV/AcAc process were proposed.

Iron in non-hydroxyl radical mediated photochemical processes for dye degradation: Catalyst or inhibitor?

The acetylacetone (AA) mediated photochemical process has been proven as an efficient approach for decoloration. For azo dyes, the UV/AA process was several to more than ten times more efficient than the UV/H2O2 process. Iron is one of the most common elements on the earth. It is well known that iron can improve the UV/H2O2 process through thermal Fenton and photo-Fenton reactions. What will be the role of iron in the UV/AA process? Could iron-AA complexes act as photocatalysts in environmental remediation? To answer these questions, the photo-degradation of an azo dye, Acid Orange 7 (AO7), was conducted under the variant combinations of AA with iron species in both ionic (Fe2+, Fe3+) and complex (Fe(AA)3) forms. The pseudo-first-order decoloration rate constants of AO7 in these photochemical processes followed such an order: UV/Fe(II)/AA<UV/Fe(III)/AA<UV/Fe(AA)3<UV/AA. The results demonstrate that iron species, in either ionic or complex form, acts as an inhibitor rather than a catalyst in the UV/AA process. Based on spectroscopic analysis, the inner filter effect of iron and the competition between Fe(III) and AA for the complexation with AO7 were attributed to the inhibition effect of iron on the UV/AA process. The understanding of the role of iron provides insight into the practical application of the UV/AA process.