Seok Won Hong

Acute toxicity of Ag and CuO nanoparticle suspensions against Daphnia magna: The importance of their dissolved fraction varying with preparation methods

A variety of methods to prepare nanoparticle suspensions have been employed for aquatic toxicity tests, although they can influence the dispersion property and subsequent toxicity of nanoparticles. Thus, in this study, we prepared stock suspensions of silver (Ag) and copper oxide (CuO) nanoparticles using different methods and compared their acute toxicity against Daphnia magna. The results showed that the dispersion method, filtration and initial concentration largely affected their toxicity, when the toxicity was expressed as the total concentrations of Ag and Cu. In case of Ag nanoparticles, the toxicity was also influenced by their different particle size. However, negligible differences in 24h-median effect concentration (EC(50)) values, which were calculated in terms of their dissolved concentrations, were observed. When expressing toxicity on the basis of dissolved concentrations, 24h-EC(50) values of the Ag and CuO nanoparticles were also found to be similar to those of the counterpart ionic species, i.e., Ag (as AgNO(3)) and Cu (as CuCl(2)·2H(2)O). These findings indicate that the dissolved fraction of nanoparticles largely contributes to their acute toxicity. Our results may help in establishing a useful guideline for preparing nanoparticle suspensions with reproducible toxicity.

Experimental evaluation of influential factors for electricity harvesting from sediment using microbial fuel cell

The aim of this study was to evaluate limiting factors affecting electricity output from sediment microbial fuel cells (sediment MFCs). In laboratory tests, various factors likely to be encountered in field application were divided into controllable and uncontrollable ones. Based on the findings, it could be suggested that the sediment MFCs can be operated with an anode to cathode area ratio of at least 5:1 and at high external loads (1000 ohms) when the cathode is closely placed to the anode, though DO concentration at the cathode must be kept above 3 mg/l. Furthermore, no significant effect on current production over a prolonged period was observed within the sediment temperature range of 20-35 degrees C, but was negatively affected by lower temperatures (10 degrees C). These observations provide important factors with respect to the construction and operation of sediment MFCs at field sites, which will aid in maximizing electricity output.

Selective Oxidative Degradation of Organic Pollutants by Singlet Oxygen-Mediated Photosensitization: Tin Porphyrin versus C60 Aminofullerene Systems

This study evaluates the potential application of tin porphyrin- and C(60) aminofullerene-derivatized silica (SnP/silica and aminoC(60)/silica) as (1)O(2) generating systems for photochemical degradation of organic pollutants. Photosensitized (1)O(2) production with SnP/silica, which was faster than with aminoC(60)/silica, effectively oxidized a variety of pharmaceuticals. Significant degradation of pharmaceuticals in the presence of the 400-nm UV cutoff filter corroborated visible light activation of both photosensitizers. Whereas the efficacy of aminoC(60)/silica for (1)O(2) production drastically decreased under irradiation with λ > 550 nm, Q-band absorption caused negligible loss of the photosensitizing activity of SnP/silica in the long wavelength region. Faster destruction of phenolates by SnP/silica and aminoC(60)/silica under alkaline pH conditions further implicated (1)O(2) involvement in the oxidative degradation. Direct charge transfer mediated by SnP, which was inferred from nanosecond laser flash photolysis, induced significant degradation of neutral phenols under high power light irradiation. Self-sensitized destruction caused gradual activity loss of SnP/silica in reuse tests unlike aminoC(60)/silica. The kinetic comparison of SnP/silica and TiO(2) photocatalyst in real wastewater effluents showed that photosensitized singlet oxygenation of pharmaceuticals was still efficiently achieved in the presence of background organic matters, while significant interference was observed for photocatalyzed oxidation involving non-selective OH radical.

Alteration of sediment organic matter in sediment microbial fuel cells

The alteration of physico-chemical properties of sediment organic matter (SOM) incubated under current-harvesting conditions as well as no-current producing conditions over 120 days using sediment microbial fuel cell systems was examined. The SOM was microbially oxidized under anaerobic conditions with an electrode serving as a terminal electron acceptor. It was found that SOM around the electrochemically-active electrodes became more humified, aromatic, and polydispersed, and had a higher average molecular weight, along with its partial degradation and electricity generation compared to that for the original sediment. These changes in SOM properties were analogous to those commonly observed in the early stages of the SOM diagenetic process (i.e. humification). Such a humification-like process was evidently more stimulated when electrical current was produced than no-current condition. These new findings associated with microbially-catalyzed electricity generation may present a potential for the energy-efficient remediation, monitoring, and/or management of the geo-environment.

Magnetite/mesocellular carbon foam as a magnetically recoverable fenton catalyst for removal of phenol and arsenic

A magnetite-loaded mesocellular carbonaceous material, Fe(3)O(4)/MSU-F-C, exhibited superior activity as both a Fenton catalyst and an adsorbent for removal of phenol and arsenic, and strong magnetic property rendering it separable by simply applying magnetic field. In the presence of hydrogen peroxide, the catalytic process by Fe(3)O(4)/MSU-F-C completely oxidized phenol and As(III) under the conditions where commercial iron oxides showed negligible effects. Notably, the decomposition of H(2)O(2) by Fe(3)O(4)/MSU-F-C was not faster than those by commercial iron oxides, indicating that hydroxyl radical produced via the catalytic process by Fe(3)O(4)/MSU-F-C was used more efficiently for the oxidation of target contaminants compared to the other iron oxides. The homogeneous Fenton reaction by the dissolved iron species eluted from Fe(3)O(4)/MSU-F-C was insignificant. At relatively high doses of Fe(3)O(4)/MSU-F-C, total concentration of arsenic decreased to a significant extent due to the adsorption of arsenic on the catalyst surface. The removal of arsenic by adsorption was found to proceed via preoxidation of As(III) into As(V) and the subsequent adsorption of As(V) onto the catalyst.

Photosensitized Oxidation of Emerging Organic Pollutants by Tetrakis C60 Aminofullerene-Derivatized Silica under Visible Light Irradiation

We recently reported that C(60) aminofullerenes immobilized on silica support (aminoC(60)/silica) efficiently produce singlet oxygen ((1)O(2)) and inactivate virus and bacteria under visible light irradiation. (1) We herein evaluate this new photocatalyst for oxidative degradation of 11 emerging organic contaminants, including pharmaceuticals such as acetaminophen, carbamazepine, cimetidine, propranolol, ranitidine, sulfisoxazole, and trimethoprim, and endocrine disruptors such as bisphenol A and pentachlorophenol. Tetrakis aminoC(60)/silica degraded pharmaceuticals under visible light irradiation faster than common semiconductor photocatalysts such as platinized WO(3) and carbon-doped TiO(2). Furthermore, aminoC(60)/silica exhibited high target-specificity without significant interference by natural organic matter. AminoC(60)/silica was more efficient than unsupported (water-suspended) C(60) aminofullerene. This was attributed to kinetically enhanced (1)O(2) production after immobilization, which reduces agglomeration of the photocatalyst, and to adsorption of pharmaceuticals onto the silica support, which increases exposure to (1)O(2) near photocatalytic sites. Removal efficiency increased with pH for contaminants with a phenolic moiety, such as bisphenol A and acetaminophen, because the electron-rich phenolates that form at alkaline pH are more vulnerable to singlet oxygenation.

Sorption of Pb(II) and Cu(II) onto multi-amine grafted mesoporous silica embedded with nano-magnetite: Effects of steric factors

Steric factors affecting the mass transfer of Pb(II) and Cu(II) in mesocellular silica foams (MSU-F-S) functionalized with multi- (mono-, di-, tri-) amine groups and nano-magnetite were investigated through batch experiments. We observed that neither the sorption capacities nor the sorption rates were linearly proportional to the number of amine groups introduced to a ligand. Unexpectedly, the tri-amine grafted samples exhibited lower affinity for both metal cations. These results are mainly attributed to two important steric factors, pore blockage and a conformational change of available amine groups. The relatively large pore size (∼30 nm) of MSU-F-S could enable various functional molecules such as amines and nano-magnetite to be effectively loaded within the pores. However, their excessive densities in the limited pore structure could have adverse effects on the transport of metal ions into the mesopores. An intraparticle diffusion model was applied to elucidate the mechanisms involved in the sorption process. Our results showed that the diffusional mass transfer into the mesopores was significantly inhibited in tri-amine grafted samples. The present findings further the understanding of steric effects on the transport of cationic metals into functionalized mesoporous silica and designing efficient sorbents.

Production of algal biomass (Chlorella vulgaris) using sediment microbial fuel cells

In this study, a novel algal biomass production method using a sediment microbial fuel cell (SMFC) system was assessed. Under the experimental conditions, CO(2) generation from the SMFC and its rate of increase were found to be dependent on the current generated from the SMFC. However, the CH(4) production rate from the SMFC was inhibited by the generation of current. When Chlorella vulgaris was inoculated into the cathode compartment of the SMFC and current was generated under 10 Ω resistance, biomass production from the anode compartment was observed to be closely associated with the rate of current generation from the SMFC. The experimental results demonstrate that 420 mg/L of algae (dry cell weight) was produced when the current from the SMFC reached 48.5 mA/m(2). Therefore, SMFC could provide a means for producing algal biomass via CO(2) generated by the oxidation of organics upon current generation.

Degradation of polycyclic aromatic hydrocarbons by ultrasonic irradiation

Polycyclic aromatic hydrocarbons (PAHs) are known to be hazardous compounds with life threatening effects as some of them are proven to be environmentally obnoxious carcinogenic compounds. Ultrasonic irradiation was investigated as a method of attacking the chemical structure of PAH compounds for a complete breakdown. This method produced very promising results with formation of hydroxyl radical (OH·), which is known as a less selective oxidant and very reactive with carbon-chlorine bonds and carbon-carbon double bonds making them capable of generating aromatic ring cleavage. Ultrasonic irradiation resulted in a decrease of PAHs with time and the dominant free radical reaction became a controlling factor. Further, hydrogen peroxide and argon gas markedly enhanced the degradation efficiency during sonolysis. With these agents, more than 30% of additional degradation efficiencies were achieved for all PAHs used in this experiment. Higher degradation efficiencies of PAHs were observed with lowering organic solvent/water ratios and pH range (acidic condition, pH 2). The apparent kinetics were first-order, with the observed rates ranging from 1.60 to 2.81 × 10−2 min−1 depending on types of PAHs and presence/absence of hydrogen peroxide and argon gas.

Titanium dioxide nanofibers integrated stainless steel filter for photocatalytic degradation of pharmaceutical compounds

A photocatalytically active stainless steel filter (P-SSF) was prepared by integrating electrospun TiO2 nanofibers on SSF surface through a hot-press process where a poly(vinylidene fluoride) (PVDF) nanofibers interlayer acted as a binder. By quantifying the photocatalytic oxidation of cimetidine under ultraviolet radiation and assessing the stability of TiO2 nanofibers integrated on the P-SSF against sonication, the optimum thickness of the TiO2 and PVDF layer was found to be 29 and 42 μm, respectively. At 10L/m(2)h flux, 40-90% of cimetidine was oxidized when the thickness of TiO2 layer increased from 10 to 29 μm; however, no further increase of cimetidine oxidation was observed as its thickness increased to 84 μm, maybe due to limited light penetration. At flux conditions of 10, 20, and 50 L/m(2) h, the oxidation efficiencies for cimetidine were found to be 89, 64, and 47%, respectively. This was attributed to reduced contact time of cimetidine within the TiO2 layer. Further, the degradation efficacy of cimetidine was stably maintained for 72 h at a flux of 10 L/m(2) h and a trans-filter pressure of 0.1-0.2 kPa. Overall, our results showed that it can potentially be employed in the treatment of effluents containing organic micropollutants.