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Objectives : Bone char is used in many eastern countries in Africa to remove high levels of fluoride from groundwater. However, due to the low adsorption efficiency of bone char, it is necessary to replace bone char frequently, which cause significant burden to the people in those areas. In this study, we developed a water treatment system to remove high level of fluoride in groundwater using a high efficiency bone char.Methods : In order to make a high efficiency bone char, cow bones were washed, dried and cut into small pieces. Then the bones were burned for 1, 3 and 5 hours at 350, 450 and 550℃ in electric furnaces. After that, the burned bones were sieved with 600~2,000 µm to match the size of bone char being used in Ethiopia. Surface analysis of bone char was performed using SEM and BET. The removal efficiency of bone char was conducted with various level of turbidity, TOC, and fluoride concentration for 90 minutes under the flow rate conditions of 100, 200, 300, and 400 L/day with an initial fluoride concentration of 4.8 mg/L.Result and Discussion : There was a significant difference between the bone char from Ethiopia and our study in terms of their surface roughness and specific surface area according to SEM and BET analysis. The adsorption capacity of the bone char produced in this study was 3.7 mg F/g, compared to 1 mg/L from the one from Ethiopia. In terms of turbidity and organic matter removal with column test, 200 L/d showed the shortest operating time to reach turbidity of less than 0.5 NTU, and was an effective operation for TOC removal. However, It took the longest to 1.5 mg/L of fluoride after breakthrough under 100 L/d operating conditions. In terms of operating time, bed volume, and energy efficiency, 100 L/d was found to be an effective operating condition.Conclusions : We developed a high efficiency bone char in this study with modification of its production process and tested it at various operating conditions. Our study showed that the bone char developed in this study is about 4 times more effective than traditional bone char and it is most effective at operation with low flow rates. Column operation is most effective at 100 L/d for fluoride removal under operating time and bed volume and energy efficiency. Therefore operating condition of drinking water treatment system for the fluorine removal using bone char in developing countries is effective in low flow rate operation.

The use of herbal medicine has increased tremendously over the last decades, generating a considerable amount of herbal medicine waste. Pyrolysis is a promising option to dispose of biomass and organic waste such as herbal medicine waste. Herein, an activated carbon-supported Pt catalyst (Pt/AC) and carbon dioxide (CO2) were applied to the pyrolysis of real herbal medicine waste to develop a thermal disposal method to prevent the formation of benzene derivatives that are harmful to the environment and human health. When using the Pt/AC catalyst in the pyrolysis of the herbal medicine waste at 500 &deg, C, the generation of benzyl species was suppressed. This was likely because the Pt catalytic sites accelerate a free radical mechanism that is dominant in the thermal cracking of carbonaceous substances. However, the employment of CO2 (instead of typically used N2) as a pyrolysis medium for the herbal medicine waste pyrolysis did not decrease the concentrations of benzyl compounds contained in the pyrolytic products of the herbal medicine waste. This study might help develop a method to thermally dispose of agricultural biowaste, preventing the formation of harmful chemicals to the environment and human beings.

In processes of manufacturing semiconductors, reactive by-products (as a form of fine powder, i.e., dust) are deposited in pipes installed on post processing and exhaust systems, potentially involving a considerable explosion risk. In this study, the effectiveness of scrubber methods (e.g., dry scrubber and burn-wet scrubber) to mitigate the risk was evaluated. To this end, three by-products generated from a ZrO

In processes of manufacturing semiconductors, reactive by-products (as a form of fine powder, i.e., dust) are deposited in pipes installed on post processing and exhaust systems, potentially involving a considerable explosion risk. In this study, the effectiveness of scrubber methods (e.g., dry scrubber and burn-wet scrubber) to mitigate the risk was evaluated. To this end, three by-products generated from a ZrO2 atomic layer deposition (ALD) process were collected from semiconductor manufacturers, which were treated with different methods (i.e., no treatment, treatment using dry scrubber, and treatment using burn-wet scrubber), and their characteristics were analyzed and compared. Particle size measurements of the by-products proved that the burn-wet scrubber treatment less decreased their particle size than the dry scrubber treatment. The burn-wet scrubber treatment made the by-product thermally stable, confirmed by thermogravimetric analysis. Fourier-transform infrared spectroscopy of the by-products before and after the scrubber treatments showed that burn-wet scrubbing of the by-product decreases surface functionalities that play a role in explosion. Dust explosion testing proved that robustness of explosion of the untreated by-product is about 7 times higher than the by-product treated with the burn-wet scrubber. Based on the results of this study, it would be suggested that burn-wet scrubber is a useful treatment method to decrease the explosion risks caused by dust by-products generated from ALD in semiconductor manufacturing processes.

There has been an accelerating increase in water reuse due to growing world population, rapid urbanization, and increasing scarcity of water resources. However, it is well recognized that water reuse practice is associated with many human health and ecological risks due to numerous chemicals and pathogenic microorganisms. Especially, the potential transmission of infectious disease by hundreds of pathogenic viruses in wastewater is one of the most serious human health risks associated with water reuse. In this study, we determined the response of different bacteriophages representing various bacteriophage groups to chlorination in real wastewater in order to identify a more reliable bacteriophage indicator system for chlorination in wastewater. Different bacteriophages were spiked into secondary effluents from wastewater plants from three different geographic areas, and then subjected to various doses of free chlorine and contact time at in a bench-scale batch disinfection system. The inactivation of was relatively rapid and reached ~4 log10 with a CT value of 5 mg/L*min. On the other hand, the inactivation of bacteriophage PRD1 and MS2 were much slower than the one for and only ~1 log10 inactivation was achieved by a CT value of 10 mg/L*min. Overall, the results of this study suggest that bacteriophage both MS2 and PRD1 could be a reliable indicator for human pathogenic viruses for chlorination in wastewater treatment processes and water reuse practice.

Arsenate in drinking water is a serious concern to millions of people around the world. Although various technologies have been developed in recent years, one of the most sustainable technologies for removing arsenate from water in developing countries is the use of absorption in the treatment of drinking water. This study determined the surface characteristics and arsenic removal efficiency of a new adsorbent Fe–Mn–Si (FM-α) and compared the performance of a hybrid system using FM-α and a microfiltration membrane with a hybrid system using a traditional adsorbent (zero-valent iron, ZVI) and a microfiltration membrane. Surface area analyses employing electron microscopy and energy-dispersive X-ray spectroscopy obtained a specific surface area of FM-α (17.2 m2/g) that is 14 times that of ZVI (1.2 m2/g). The arsenate removal efficiency of FM-α was 51 and 14% at pH 4 and 7, respectively, in the presence of phosphate, and 89 and 94% at pH 4 and 7, respectively, in the presence of humic acid; all these...

The purpose of this study was to analyse the runoff characteristics of non-point pollution sources in an urban watershed and determine the effectiveness of newly installed riverwater treatment system to reduce water pollution caused by storm runoff in the urban watershed. The results of this study showed that the levels of BOD5 and suspended solid were highly influenced by first-flush effect and the pollutant load of those two parameters were also very high in the urban watershed. Meanwhile, the effectiveness of riverwater treatment system to reduce the levels of BOD5 and suspended solid was relatively high, but those to reduce the levels of T-N and T-P was low, which needs some additional unit treatment process such as filtration and coagulation. Nonetheless, the riverwater treatment system tested was relatively simple in installation and operation, effective in removing many water pollutants and, most importantly, does not require much space as other treatment systems, so it could be an attractive alternative option to reduce riverwater pollution caused by storm runoff in urban watersheds.

The high cost and environmental issues associated to the fluoride removal technologies as well as their continuous and excessive applications display several challenges in groundwater remediation. This study discusses the fluoride removal potential of bone char prepared from the bone residue. The influence of pyrolysis conditions on the physiochemical properties of the bone char is examined. The bone char synthesized under modest conditions was characterized using a field emission scanning electron microscope, energy dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy and X-ray diffraction. It was found that fluoride adsorption declines with rising the calcination temperature. The bone char samples prepared under N2 environment indicated higher adsorption as compared with the samples prepared under air environment. 4.29 mg of fluoride is adsorbed on 1 g of bone char prepared at 350 °C under N2 environment while, this value was dropped to 2.91 mg g−1 when bone char is synthesized at 700 °C. However, under air environment, the adsorption was 3.63 and 0.16 mg g−1 for bone chars prepared at 350 and 700 °C, respectively. The packed bed columns were operated with different size of particle (150–425 μm) and EBCT (0.5 & 1 h). Columns effectively treated the fluoride containing influent (10 mg L−1) and achieved acceptable level in a short EBCT. This study displayed the great potential of bone char usage in fluoride affected areas.

Polyaniline (PANI) is a promising conducting polymer for surface modification of TiO2 to achieve extended photoresponse to visible light and increased photocatalytic efficiency. In this study, we report the synthesis of a PANI/TiO2 composite with different weight ratios of PANI, which was subsequently employed for photocatalytic degradation of methylene blue (MB), bisphenol A (BPA), and bacteriophage MS2 under visible-light irradiation. The functional groups, morphology, and light response of the composite were characterized by Fourier-transform infrared spectroscopy, field-emission transmission electron microscopy, and diffuse reflectance UV&ndash, visible spectroscopy, respectively. The PANI/TiO2 composite containing 4% by weight ratio of PANI was most suitable for MB degradation, and this photocatalyst was very stable even after repeated use (four cycles). The degradation of BPA and bacteriophage MS2 by PANI/TiO2 composite reached 80% in 360 min and 96.2% in 120 min, respectively, under visible-light irradiation. Therefore, the PANI/TiO2 composite with enhanced visible-light photocatalytic efficiency and stability can be widely used for the degradation of water contaminants.

One of the biggest challenges in reverse osmosis membrane process is formation of biofilms on membrane surface (biofouling) which significantly lowers membrane performance and shortens life cycle of the membrane. In an effort to find a more effective biocide to control biofouling, we investigated the potential of N-chlorosuccinimide (NCS) as a biofouling control agent in polyamide membrane. The results of this study show that there are no significant changes in the surface characteristics of polyamide membrane (measured by X-ray photoelectron spectroscopy (XPS) and attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR)) when it is exposed to a high concentration of NCS (5000 mg/L as Cl2). Also, there were no significant changes in membrane performance based on permeate flux and salt rejection after exposure to the same concentration of NCS. Most importantly, inactivation of Pseudomonas aeruginosa PAO1 GFP biofilm cells by 10 mg/L of NCS was 2.2 log after 30 min, which is far greater than that of chlorine. Overall, the results of this study suggest that NCS is a promising novel agent for biofouling control in polyamide membrane processes due to its effective inactivation of biofilm cells on membrane and minimum effect on membrane structure and performance.

In this study, we determined the removal of a prototype human norovirus (Norwalk virus, NV) by bench-scale alum coagulation, flocculation and sedimentation processes using reverse transcriptase polymerase chain reaction (RT-PCR) for norovirus assays. After determining optimum conditions for the coagulation, flocculation and sedimentation processes in terms of turbidity reduction, jar tests were performed using the same waters seeded with test viruses. For comparison, two other important health-related viruses, poliovirus 1 (PV1) and coliphage MS2, were included in this study. The removal of NV by coagulation, flocculation and sedimentation processes based on RT-PCR assay in this study was 1.5 log10, which was similar to that of PV1 and a little lower than that of coliphage MS2 (2 log10) based on the same RT-PCR assay. The removal of NV in this study (1.5 log10) is considerably higher than the one in a recent study using recombinant norovirus virus-like particles (∼0.7 log10). Overall, the results of this study suggest that human noroviruses can be appreciably reduced by a properly-operated coagulation, flocculation and sedimentation processes and the contamination of drinking water by noroviruses should be controlled by conventional water treatment processes with conventional physico-chemical processes and disinfection.

There has been growing concern over human exposure to adenoviruses through drinking water due to the extreme resistance of human adenoviruses to the traditional UV technology (low-pressure (LP) UV). As an effort to develop an effective treatment strategy against human adenoviruses in drinking water, we determined the effectiveness of sequential disinfection with an alternative UV technology (medium-pressure (MP) UV) and free chlorine. Human adenovirus 2 (Ad2) was irradiated with a low dose of MP UV irradiation (10 mJ/cm2) through UV collimated apparatus and then exposed to a low dose of free chlorine (0.17 mg/L) at pH 8 and 5°C using a bench-scale chemical disinfection system. A significant inactivation (e.g. 4 log10) of Ad2 was achieved with the low doses of MP UV and free chlorine within a very short contact time (∼1.5 min) although there was no apparent synergistic effect on Ad2 between MP UV and free chlorine. Overall, it is likely that the sequential disinfection with UV irradiation and free chlorine should control the contamination of drinking water by human adenoviruses within practical doses of UV and free chlorine typically used in drinking water treatment processes.

Aims: In this study, we determined the ability of a promising alternative UV technology – a polychromatic emission from a medium-pressure UV (MP UV) technology – to inhibit the reactivation of UV-irradiated Giardia lamblia cysts. Methods and Results: A UV-collimated beam apparatus was used to expose shallow suspensions of purified G. lamblia cysts in PBS (pH 7·2) or filtered drinking water to a low dose (1 mJ cm−2) of MP UV irradiation. After UV irradiation, samples were exposed to two repair conditions (light or dark) and two temperature conditions (25°C or 37°C for 2–4 h). The inactivation of G. lamblia cysts by MP UV was very extensive, and c. 3 log10 inactivation was achieved with a dose of 1 mJ cm−2. Meanwhile, there was no apparent reactivation (neither in vivo nor in vitro) of UV-irradiated G. lamblia under the conditions tested. Conclusion: The results of this study indicated that, unlike the traditional low-pressure (LP) UV technology, an alternative UV technology (MP UV) could inhibit the reactivation of UV-irradiated G. lamblia cysts even when the cysts were exposed to low UV doses. Significance and Impact of the Study: It appears that alternative UV technology has some advantages over the traditional LP UV technology in drinking water disinfection because of their high level of inactivation against G. lamblia cysts and also effective inhibition of reactivation in UV-irradiated G. lamblia cysts.

In an effort to validate previous research suggesting remarkable resistance of norovirus to free chlorine disinfection, we characterized the disinfection response of purified and dispersed Norwalk virus (NV) by bench-scale free chlorine disinfection using RT-PCR for virus assays. The inactivation of NV by two doses of free chlorine (1 and 5mg/L) at pH 6 and 5 degrees C based on two RT-PCR assays was similar to that of coliphage MS2, but much faster than that of poliovirus 1. Despite the underestimation of virus inactivation by RT-PCR assays, the predicted CT values for NV based on RT-PCR assays are lower than the ones for most other important waterborne viruses and the CT guidelines for chlorine disinfection of viruses under the Surface Water Treatment Rule by the United States Environmental Protection Agency. Overall, the results of this study indicate that NV is not highly resistant to free chlorine disinfection as suggested by previous research and it is likely that NV contamination of drinking water can be controlled by adequate free chlorine disinfection practices with provision of proper pre-treatment processes before chlorination.

In this study, we determined the repair capabilities of Giardia lamblia cysts when they were exposed to low-pressure (LP) UV and then 4 different repair conditions. A UV collimated beam apparatus was used to expose shallow suspensions of G. lamblia cysts in buffered reagent water (PBS, pH 7.2) to various doses of LP UV irradiation. After UV irradiation, samples were exposed to 4 repair conditions (light and dark repair conditions with 2 temperatures (25 °C and 37 °C) for each condition). The inactivation of G. lamblia cysts by LP UV was very extensive (∼5 log10) even with a low dose of LP UV (1 mJ/cm2). More importantly, there was significant restoration of infectivity in G. lamblia cysts when they were exposed to a low dose of LP UV and then to all the repair conditions tested. Overall, the results of this study indicate that G. lamblia cysts do have the ability to repair their UV-damaged DNA when they are exposed to low doses of LP UV irradiation. This is the first study to report the presence of repair in UV-irradiated G. lamblia cysts.

To elucidate the roles of physical and chemical properties of viruses and their sensitivity to UV radiation, the kinetics and extent of inactivation of several waterborne pathogenic viruses and bacteriophages with different virion sizes and genomic composition by monochromatic, low-pressure (LP) UV was determined in phosphate buffered saline or a filtered drinking water. The inactivation rates of the small RNA viruses, poliovirus 1 and Coxsackievirus B4, by LP UV were very rapid and reached ~4 log10 and >5 log10, respectively, within a UV dose of 30 mJ/cm2. In contrast, the inactivation of the small RNA bacteriophage, MS2, was much slower and only 2 log10 inactivation was achieved at a UV dose of 30 mJ/cm2. The inactivation of the large DNA virus, adenovirus 2, was relatively slow and only 2 log10 inactivation was achieved with a UV dose of 60 mJ/cm2. In contrast, the inactivation rates of the three large DNA bacteriophages were very rapid and reached >5 log10 with a UV dose of 10 mJ/cm2. Therefore, the results of this study indicate that inactivation of human enteric viruses and bacteriophages by UV irradiation is not simply predictable by the type and size of the virus or its nucleic acid genome and there is no strong correlation between virion size and genetic composition of enteric viruses and their response to LP UV irradiation. Key words: low pressure ultraviolet (LP UV), poliovirus 1, Coxsackievirus B4, bacteriophage MS2, bacteriophage PRD1, adenovirus 2, UV disinfection.

The Greater Cincinnati (Ohio) Water Works strives to continually improve the effectiveness of its water treatment processes. Questions regarding the vulnerability of the Ohio River watershed to microbial contamination and concerns about compliance with the Long Term 2 Enhanced Surface Water Treatment Rule led the utility to initiate an in-depth study of ultraviolet (UV) disinfection. The study was designed to determine how exposing treated Ohio River water to UV affected (1) the inactivation of Cryptosporidium parvum, bacteria, and viruses, (2) the susceptibility of these microorganisms to free chlorine after partial inactivation with UV, (3) the formation of oxidation and chlorinated disinfection by-products (DBPs), and (4) microbial regrowth (measured by assimilated organic carbon) following UV disinfection. Results indicated that UV alone or UV followed by free chlorine effectively controlled all microorganisms tested. Additionally, no evidence of increased DBP formation or regrowth was observed at UV doses typically used for disinfection.

Norwalk virus and other human caliciviruses (noroviruses) are major agents of gastroenteritis, and water is a major route of their transmission. In an effort to control Norwalk virus in drinking water, Norwalk virus reduction by bench-scale ozone disinfection was determined using quantitative reverse transcription (RT)-PCR for virus assays. Two other enteric viruses, poliovirus 1 and coliphage MS2, were included for comparison, and their reductions were assayed by infectivity assays as well as by RT-PCR. Virus reductions by ozone were determined using a dose of 0.37 mg of ozone/liter at pH 7 and 5°C for up to 5 min. Based on two RT-PCR assays, the reductions of Norwalk virus were >3 log 10 within a contact time of 10 s, and these were similar to the reductions of the other two viruses determined by the same assay methods. Also, the virus reductions detected by RT-PCR assays were similar to those detected by infectivity assays, indicating that the RT-PCR assay is a reliable surrogate assay for both culturable and nonculturable viruses disinfected with ozone. Overall, the results of this study indicate that Norwalk virus as well as other enteric viruses can be reduced rapidly and extensively by ozone disinfection and that RT-PCR is a useful surrogate assay for both culturable and nonculturable viruses disinfected with ozone.

UNLABELLED There has been a growing concern over human exposure to Mycobacterium avium subspecies hominissuis (MAH) through drinking water due to its ubiquitous presence in natural waters and remarkable resistance to both chemical and physical disinfectants in drinking water treatment processes. However, little is known about the effectiveness of physico-chemical water treatment processes to remove MAH. Therefore, we determined the removal of MAH by alum coagulation, flocculation and sedimentation processes in optimized drinking water treatment conditions using standard jar test equipment. Contrary to the prevailing hypothesis, the results of this study show that removal of MAH by coagulation, flocculation and sedimentation processes was only moderate (approx. 0.65 log10) under low turbidity treatment conditions and the removal of MAH was actually lower than that of Escherichia coli (reference bacterium) in all the waters tested. Overall, the results of this study suggested that coagulation, flocculation and sedimentation processes may not be a reliable treatment option for removing MAH, and more efforts to find an effective control measures against MAH should be made to reduce the risk of MAH infection from drinking water. SIGNIFICANCE AND IMPACT OF THE STUDY Despite a growing concern over human exposure to Mycobacterium avium subspecies hominissuis (MAH) through drinking water and its remarkable resistance to water disinfectants, little is known about the effectiveness of physico-chemical water treatment processes to remove MAH. Contrary to the prevailing hypothesis, the results of this study suggest that coagulation, flocculation and sedimentation processes may not be a reliable treatment option for MAH removal. As these processes have been the last remaining conventional drinking water treatment processes that might be effective against MAH, more efforts should be urgently made to find an effective control measures against this important waterborne pathogen.

Because Cryptosporidium parvum oocysts are very resistant to conventional water treatment processes, including chemical disinfection, we determined the kinetics and extent of their inactivation by monochromatic, low-pressure (LP), mercury vapor lamp UV radiation and their subsequent potential for DNA repair of UV damage. A UV collimated-beam apparatus was used to expose suspensions of purified C. parvum oocysts in phosphate-buffered saline, pH 7.3, at 25°C to various doses of monochromatic LP UV. C. parvum infectivity reductions were rapid, approximately first order, and at a dose of 3 mJ/cm 2 (=30 J/m 2 ), the reduction reached the cell culture assay detection limit of ∼3 log 10 . At UV doses of 1.2 and 3 mJ/cm 2 , the log 10 reductions of C. parvum oocyst infectivity were not significantly different for control oocysts and those exposed to dark or light repair conditions for UV-induced DNA damage. These results indicate that C. parvum oocysts are very sensitive to inactivation by low doses of monochromatic LP UV radiation and that there is no phenotypic evidence of either light or dark repair of UV-induced DNA damage.

Cryptosporidium parvum oocysts in water were exposed to distinct wavelength bands of collimated beam ultraviolet (UV) radiation across the germicidal UV wavelength range (210-295 nm) that were emitted from a medium pressure (MP) mercury vapour lamp. The dose of UV radiation transmitted though each narrow bandpass filter was measured utilising potassium ferrioxalate actinometry. Oocyst infectivity was determined using a cell culture assay and titre was expressed as an MPN. The log10 inactivation for each band of radiation was determined for a dose of 2 mJ/cm2. Doses from all wavelengths between 250-275 nm resulted in approximately 2 log10 inactivation of Cryptosporidium parvum oocyst infectivity while doses with wavelengths higher and lower than this range were less effective. Because polychromatic radiation from MP UV lamps had about the same germicidal activity between the wavelengths of 250-275 nm for inactivation of oocyst infectivity, there was no unique advantage of MP UV over low pressure (LP) UV except for the simultaneous delivery of a wide range of germicidal wavelengths.

In an effort to reduce human exposure to adenoviruses through drinking water, we determined the effectiveness of sequential disinfection with an alternative ultraviolet (UV) technology (medium-pressure (MP) UV) and monochloramine. The results of this study showed that MP UV was much more effective than traditional UV technology (low-pressure (LP) UV) against human adenovirus 2 (Ad2). Specifically, an inactivation of ~3 log10 was achieved by a dose of 40 mJ/cm2 of MP UV compared to ~1 log10 by the same dose of LP UV. However, because of the ineffective inactivation of Ad2 by monochloramine, a very high dose (40 mJ/cm2) of MP UV and a very large Ct99 value (~1200 mg/L·min) was still needed to achieve a significant inactivation (e.g., 4 log10) of Ad2. Also, it appears that the inactivation of Ad2 by monochloramine is not enhanced by prior exposure to MP UV. Overall, the results of this study indicated that, in spite of the enhanced effectiveness of alternative UV technologies on human adenoviruses, sequential disinfection with an alternative UV technology (MP UV) and monochloramine still may not provide adequate inactivation of human adenoviruses — especially at high pH and low temperature — in drinking water treatment processes.

Human enteric viruses are important agents of waterborne illness. They are diffusely distributed in environmental waters, necessitating concentration of tens to hundreds of litres for effective detection. This study evaluates the novel ViroCap disposable capsule filter for concentration of coliphage MS2 and poliovirus (PV1) from deionised (DI) water and artificial seawater, as well as natural ground, surface, and seawater. Retention and recoveries for the ViroCap were compared with two well-characterised filters: the 1MDS for DI water, and the OptiCap XL for artificial seawater. The mean adsorption for MS2 by the ViroCap was 88%. Recovery of MS2 was significantly greater (p ≤ 0.01) than alternative filters tested: 65% from DI water and 63% from artificial seawater, compared to 30% for the 1MDS and 15% for the OptiCap for the respective matrices. Recovery of PV1 from DI water (37%) was similar to that of the 1MDS (51%). PV1 recoveries from artificial seawater were significantly greater (p ≤ 0.01) for the ViroCap (44%) than the OptiCap (11%). Recovery of MS2 from seeded environmental samples yielded 44% from groundwater, 53% from surface water, and 51% from seawater. ViroCap disposable filter is efficient for concentrating MS2 and PV1 from diverse matrices and is robust across a range of ionic concentrations.

Although the efficacy of chlorine disinfection under controlled laboratory conditions is well known, the effectiveness of chlorine under field point-of-use (POU) conditions is still not clearly understood and may be impacted by a variety of factors. This study evaluated the effectiveness of POU chlorine disinfection in rural Ecuador under typical use conditions and compared this effectiveness with the efficacy in controlled laboratory conditions. While reductions of indicator organisms were slightly higher in households that used chlorination, no significant differences were seen between households employing POU chlorination and the households with no chlorination (1–1.5 log10 median reductions for chlorinating households and 0.31–0.55 log10 for nonchlorinating households, depending on the indicator organism). In contrast, significant reduction of all test organisms was found when simulating POU conditions in the laboratory. This study demonstrates that POU chlorination can be considerably less effective under actual field conditions than would be predicted based on its laboratory efficacy (3–5 log10 median reductions for chlorinated and 0–0.3 log10 for non-chlorinated samples). Human factors (including improper storage and chlorine dosing) and uncontrolled water quality effects are hypothesized to impact significantly the effectiveness of chlorine disinfection.

There has been growing concern over human exposure to adenoviruses through drinking water due to their apparent high resistance to UV irradiation and the anticipated widespread use of ultraviolet (UV) disinfection in drinking water treatment processes. However, most inactivation studies on adenoviruses were performed using only one type of UV technology—low-pressure (LP) UV, and little is known about the effectiveness of different UV technologies such as medium- pressure (MP) UV or other polychromatic UV technologies. In this work, the kinetics and extent of inactivation of a human adenovirus (adenovirus 2 (Ad2)) by both monochromatic LP and polychromatic MP UV were evaluated to determine the effectiveness of these UV technologies on human adenoviruses. Inactivation of Ad2 by LP UV was very slow and only 0.87 and 2.17 log10 inactivation was achieved with UV doses of 30 and 90 mJ/cm2, respectively. However, inactivation of Ad2 by MP UV was much faster and 2.19 and 5.36 log10 inactivation was observed with the same UV doses (30 and 90 mJ/cm2, respectively). It appears that MP UV is more effective against Ad2 than LP UV and the enhanced effectiveness of MP UV on Ad2 is likely due to its ability to inhibit the repair process in UV-irradiated Ad2.

Aims: Giardia lamblia is one of the most important waterborne pathogens in the world. In this study, we determined the effectiveness of a promising alternative UV technology – a polychromatic emission from a medium-pressure (MP) UV lamp – against G. lamblia cysts in phosphate buffered saline (PBS) and a filtered drinking water. Methods and Results: A UV collimated beam apparatus was used to expose shallow suspensions of purified G. lamblia cysts in PBS or a filtered drinking water and the UV-irradiated G. lamblia cysts were assayed in Mongolian gerbils. The inactivation of G. lamblia cysts was very rapid and reached a detection limit of >3 log10 within a UV dose of 1 mJ cm−2. Conclusion: The results of this study indicate that MP UV irradiation is very effective against G. lamblia cysts in both PBS and a filtered drinking water. Significance and Impact of the Study: It is likely that contamination of drinking water by G. lamblia cysts can be readily controlled by typical MP UV disinfection practises.

The human and animal pathogen Giardia lamblia is a waterborne risk to public health because the cysts are ubiquitous and persistent in water and wastewater, not completely removed by physical-chemical treatment processes, and relatively resistant to chemical disinfection. Given the recently recognized efficacy of UV irradiation against Cryptosporidium parvum oocysts, the inactivation of G. lamblia cysts in buffered saline water at pH 7.3 and room temperature by near monochromatic (254 nm) UV irradiation from low-pressure mercury vapor lamps was determined using a "collimated beam" exposure system. Reduction of G. lamblia infectivity for gerbils was very rapid and extensive, reaching a detection limit of4 log within a dose of 10 JM-2. The ability of UV-irradiated G. lamblia cysts to repair UV-induced damage following typical drinking water and wastewater doses of 160 and 400 JM(-2) was also investigated using experimental protocols typical for bacterial and eucaryotic DNA repair under both light and dark conditions. The infectivity reduction of G. lamblia cysts at these UV doses remained unchanged after exposure to repair conditions. Therefore, no phenotypic evidence of either light or dark repair of DNA damage caused by LP UV irradiation of cysts was observed at the UV doses tested. We conclude that UV disinfection at practical doses achieves appreciable (much greater than 4 log) inactivation of G. lamblia cysts in water with no evidence of DNA repair leading to infectivity reactivation.

The reduction of Norwalk virus (NV) by a 2 mg/L dose of pre-formed monochloramine was determined at pH 8 and 5°C in bench-scale, batch disinfection experiments using quantitative RT-PCR for NV assays. Two other enteric viruses, poliovirus 1 (PV1) and coliphage MS2, were included for comparison and assayed by infectivity as well as RT-PCR. After 3h, reductions of PV1 and MS2 by infectivity assays were about 1 log 10 but there were no reductions of these viruses by RT-PCR assays. Hence, RT-PCR underestimated virus inactivation by monochloramine. However, NV reduction by monochloramine was about 1 log 10 by RT-PCR assay, suggesting that it is more susceptible to monochloramine than the other two viruses tested. Based on RT-PCR titre reduction, the CT 99 value for NV was about 775 mg-min/L. If the reduction of NV infectivity by monochloramine is ever greater than the reduction of RT-PCR signals, the CT 99 value would be smaller. However, the results of this study indicate that NV and the other enteric viruses tested are not rapidly and extensively reduced by disinfection with pre-formed monochloramine.

Nucleic acid (NA) amplification techniques are useful to detect viruses in water and other environmental samples because they are highly sensitive, specific and can detect fastidious enteric viruses that do not grow well or not at all in cell cultures. However, RT-PCR was found to detect inactivated viruses. In terms of risks to public health this constitutes a false positive result, as inactivated viruses are no longer infectious. When poliovirus type 1 and coliphage MS2 were studied for (a) persistence in water and sewage and (b) inactivation in water by free chlorine, chlorine dioxide and UV radiation, RT-PCR assays underestimated virus inactivation. The use of multiple RT-PCR amplification sites, larger RT-PCR genomic targets and immunocapture RT-PCR sometimes reduced, but did not eliminate, the discrepancy between loss of infectivity and loss of RT-PCR titre. Virus presence based on RT-PCR detection must be interpreted with caution when predicting human health risks.