Inactivation of Escherichia coli in the electrochemical disinfection process using a Pt anode

Recently, the electrochemical disinfection has gained a great interest as one of the alternatives to conventional chlorination due to its high effectiveness and environmental compatibility. Despite the extensive reports on electro-chlorination disinfection, few researches were reported on the systems without generating chlorine. This study mainly focused on the potential disinfecting ability of electro-generated oxidants other than chlorine with using an inert medium (chloride-free phosphate buffer solution), which was intended to exclude the formation of chlorine during the electrolysis, as the Escherichia coli as an indicator bacterium was disinfected by applying the current to a platinum anode. The electrochemical inactivation of E. coli without chlorine production was demonstrated to occur in two distinct stages. The first stage inactivation takes place rapidly at the beginning of electrolysis, which appears to be achieved by the electrosorption of negatively charged E. coli cells to the anode surface, followed by a direct electron transfer reaction. As the electrolysis continues further, the inactivation becomes slower but steady, in contrast to the first stage of inactivation. This was attributed to the action of reactive oxidants generated from water discharge, such as hydroxyl radical. Overall, this study suggests that the electrochemical disinfection could be successfully performed even without producing chlorine, recommending the potential application for disinfecting water that does not allow including any chloride ions (such as the production of ultra-pure sterilized water for semiconductor washing).     

WATER MANAGEMENT AND N,P LOSSES FROM PADDY FIELDS IN SOUTHERN KOREA1

ABSTRACT: Assessment and control of nutrient losses from paddy fields is important to protect water quality of lakes and streams in Korea. A four‐year field study was carried out to investigate water management practices and losses of nitrogen (N) and phosphorus (P) in rice paddy irrigation fields in southern Korea. The amount and water quality of rainfall, irrigation, surface drainage, and infiltration were measured and analyzed to estimate inputs and losses of N and P. The observed irrigation amount surpassed consumptive use, and approximately 52 to 69 percent of inflow (precipitation plus irrigation) was lost to surface drainage. Field data showed that significant amounts of irrigation water and rainfall were not effectively used for rice paddy culture. Water quality data indicated that drainage from paddy fields could degrade the recipient water environment. The nutrient balance indicated that significant amounts of nutrients (29.5 percent of total N and 8.6 percent of total P compared to input) were lost through surface drainage. Furthermore, up to half the nutrient losses occurred during nonstorm periods. The study results indicate that inadequate water management influences N and P losses during both storm and nonstorm periods. Proper water management is required to reduce nutrient losses through surface drainage from paddy fields; this includes such measures as minimum irrigation, effective use of rainfall, adoption of proper drainage outlet structures, and minimized forced surface drainage.     

Radon concentrations in groundwater in Busan measured with a liquid scintillation counter method

In this paper, we present the first measurement of radon concentrations in drinking groundwater from private and public deep-bored wells located in the south-eastern area of Korea. The measurements were carried out on 439 samples by using a liquid scintillation method. The results show that the radon concentrations of the samples range from 0 to about 300 Bq l(-1). We find that Sasang ward shows the highest median value of radon concentration among 13 different wards, while Jung ward has the lowest. We find that the radon concentrations are highly dependent on the type of geological rock aquifers.     

Combined effect of natural organic matter and surfactants on the apparent solubility of polycyclic aromatic hydrocarbons

Both natural organic matter (NOM) and surfactants are known to enhance the apparent aqueous solubility of hydrophobic organic contaminants (HOCs) in aqueous systems. In this study, the combined effect of NOM and surfactants on enhancing the solubility of HOCs was investigated, since both may occur and affect the fate and transport of HOCs in natural aqueous environments. Experimental results indicated that the apparent solubility of naphthalene, phenanthrene, and pyrene in NOM and anionic surfactant solution was lower than their solubility in NOM solution alone. However, the apparent solubility of an HOC in NOM and nonionic surfactant solution is almost the same as the sum of the HOC's solubility in NOM solution plus its solubility in nonionic surfactant solution. The observation that apparent aqueous solubility of HOCs in NOM and anionic surfactant solution is decreased is probably due to the fact that the cations that are released when the anionic surfactant dissociates may form ion pairs with acidic or phenolic groups associated with the NOM. This serves to increase the size of hydration of these groups, thereby decreasing the effective size of the nonpolar moieties associated with the NOM, and thus decreasing hydrophobic partitioning of the HOCs into the NOM. The results presented here will help us to understand the effect of NOM and surfactants on the fate and transport of HOCs in aquatic systems.     

Concentrations and activity ratios of uranium isotopes in the groundwater of the Okchun Belt in Korea.

Groundwater samples obtained from the Okchun Belt in Korea were separated into particulate and filtered fraction using a 0.45 microm membrane filter and concentrations and activity ratios of uranium isotopes in the fractions were determined by chemical separation and alpha-spectrometric measurements. Most of the uranium isotopes in the groundwater were found in the filtered water. Only less than 1% of the total uranium was detected in the particulate fraction. The concentrations and activity ratios of uranium isotopes in the groundwater measured in this study were variable, depending upon sampling site. Owing to a rapid material exchange between the subterranean hot waters and the rock strata, the concentrations of 238U in the groundwater in the hot spring area were found to be about four times higher than those elsewhere. Because of the alpha-particle recoil effect, the activity ratios of 234U/238U in the groundwater taken at "cold" spring sites were variable within the range 1.20 to 3.58, depending on the residence time of the groundwater. In the hot spring area, the activity ratios of 234U/238U were close to the equilibrium value (1.10 +/- 0.07) due to rapid erosion of the rock strata by the hot spring water.     

Comparison of Fe(VI) (FeO4(2-)) and ozone in inactivating Bacillus subtilis spores

The protozoan parasites such as Cryptosporidiumparvum and Giardialamblia have been recognized as a frequent cause of recent waterborne disease outbreaks because of their strong resistance against chlorine disinfection. In this study, ozone and Fe(VI) (i.e., FeO(4)(2-)) were compared in terms of inactivation efficiency for Bacillus subtilis spores which are commonly utilized as an indicator of protozoan pathogens. Both oxidants highly depended on water pH and temperature in the spore inactivation. Since redox potential of Fe(VI) is almost the same as that of ozone, spore inactivation efficiency of Fe(VI) was expected to be similar with that of ozone. However, it was found that ozone was definitely superior over Fe(VI): at pH 7 and 20°C, ozone with the product of concentration×contact time (CˉT) of 10mgL(-1)min inactivate the spores more than 99.9% within 10min, while Fe(VI) with CˉT of 30mgL(-1) min could inactivate 90% spores. The large difference between ozone and Fe(VI) in spore inactivation was attributed mainly to Fe(III) produced from Fe(VI) decomposition at the spore coat layer which might coagulate spores and make it difficult for free Fe(VI) to attack live spores.     

Gas-phase elemental mercury removal in a simulated combustion flue gas using TiO2 with fluorescent light

A previously proposed technology incorporating TiO₂ into common household fluorescent lighting was further tested for its Hg⁰ removal capability in a simulated flue-gas system. The flue gas is simulated by the addition of O₂, SO₂, HCl, NO, H₂O, and Hg⁰, which are frequently found in combustion facilities such as waste incinerators and coal-fired power plants. In the O₂ + N₂ + Hg⁰ environment, a Hg⁰ removal efficiency (η_Hg) greater than 95% was achieved. Despite the tendency for η_Hg to decrease with increasing SO₂ and HCl, no significant drop was observed at the tested level (SO₂: 5–300 ppm_v, HCl: 30–120 ppm_v). In terms of NO and moisture, a significant negative effect on η_Hg was observed for both factors. NO eliminated the OH radical on the TiO₂ surface, whereas water vapor caused either the occupation of active sites available to Hg⁰ or the reduction of Hg₀ by free electron. However, the negative effect of NO was minimized (η_Hg > 90%) by increasing the residence time in the photochemical reactor. The moisture effect can be avoided by installing a water trap before the flue gas enters the Hg⁰ removal system.

Implications: This paper reports a novel technology for a removal of gas-phase elemental mercury (Hg⁰) from a simulated flue gas using TiO₂-coated glass beads under a low-cost, easily maintainable household fluorescent light instead of ultraviolet (UV) light. In this study, the effects of individual chemical species (O₂, SO₂, HCl, NO, and water vapor) on the performance of the proposed technology for Hg⁰ removal are investigated. The result suggests that the proposed technology can be highly effective, even in real combustion environments such as waste incinerators and coal-fired power plants.     

Demonstration of a high throughput on-board hydrogen generation reactor system using aluminum coil as fuel for a vehicle

A novel on-board hydrogen generation concept using Al coil with NaOH was investigated. The reaction rate was successfully controlled by introducing a pumping system for the NaOH solution. The time for the flow to develop fully was mainly dependent on the solution temperature, and the fastest start time recorded was 60 sec at a solution temperature of 70°C. The maximum H₂ generation rate was 200 L min^–1 with a prototype design of the on-board hydrogen generation system 1/8 times the size of a full-size reactor. The H₂ generation process coupled with the solution pumping system was simulated with three-dimensional fluid dynamic software, and the calculated H₂ flow and temperature rise of the system were validated with experimental data.     

Online Water Monitoring Method as a Water Security Tool: A Feasibility View

Since the tragic event on September 11, 2001 (9/11), homeland security has been the center of major attention not only in the United States but also around the world. Among homeland security agenda, more concerns on drinking water system have been drawn into the forefront attention from the public and water industry. Governmental agencies have been called upon to strongly protect the water resources from becoming a possible terror target. The online monitoring of a water system offers the potential to reduce the possible danger from a terrorist contamination as well as from unintentional chemical spills. As potential terrorist contaminants, seven chemical compounds (aldicarb, cycloheximide, dicrotophos, nicotine, sodium arsenate, sodium cyanide, and sodium fluoroacetate) were studied at different doses, in order to determine their detectability when they are present in a water system, including intake, treatment, and distribution. These contaminants were monitored by measuring simple water quality parameters such as conductivity, pH, chlorine residual, turbidity, total organic carbon (TOC), and UV254. Results indicated that the contaminants used for the study were detected at certain toxicity concentrations through the online water quality monitoring method. This method provides a useful tool for watching water resources against possible terror attacks, and also keeping safe water quality.