The presence of bromide in drinking water typically leads to the formation of brominated DBPs upon chlorination. Bromide is not removed by conventional water treatment processes. Ion-exchange and high-pressure membrane filtration remove bromide but produce a concentrated brine waste stream. One emerging technology for bromide removal is electrolysis. Limited design data on bromide removal by electrolysis are available in the literature. However, design parameters, operational constraints, and costs need to be defined. The objectives of the study were to (1) determine operational conditions under which electrolysis removes bromide and decreases the formation of halogenated disinfection by-products (DBPs); (2) investigate the effect of electrolysis on ozonation DBPs (bromate), bacterial regrowth, and taste andor; (3) evaluate the impact of electrolysis on conventional coagulation/flocculation/sedimentation and ozonation; (4) evaluate scalability and conceptual design issues; (5) determine preliminary capital and operational costs; and (6) determine future needs for demonstrating the technology. A four phased-approach was undertaken to conduct this project. During the first phase, the electrolytic reactor was designed, constructed, and activated. During the second phase, the electrolytic reactor was operated under several conditions of hydraulic residence time, current level, and influent bromide level. Key analytical parameters were measured, including bromide, bromine, chlorine, and THM and HAA concentrations. During the third phase, conventional treatment consisting of coagulation/flocculation/sedimentation and/or ozonation was tested downstream of electrolysis to investigate whether electrolysis is feasible in a conventional treatment plant context. During the fourth phase, scale up, safety, and conceptual design issues were identified and preliminary costs estimated. A workshop was held towards the end of the study to identify future needs.
Microbial contamination of drinking water and waterborne disease outbreaks continue to present a significant concern for the water industry. There is a need for pathogen detection methods that (1) incorporate sensitive detection and identification at the species/strain level, (2) have the ability to process many samples simultaneously, (3) involve minimal risk of false identification, (4) are adaptable, and (5) contain the capacity for some degree of automation. Molecular-based assays in high-throughput multi-well formats meet these requirements.? The demonstration of the feasibility of a microplate-based rapid screening assay indicates that the water industry should continue to pursue and fund exploratory research into the development of innovative pathogen detection methods. Such techniques may be used for routine screening of drinking water during outbreak situations, or to investigate episodes of intentional contamination. All of these situations require pathogen detection tools that can generate results, even if the results are only presumptive, in as short a time as possible. The assay may be linked to direct nucleic extraction methods so that all potential pathogens can be screened in a sample, thereby uncoupling the assay from time-consuming and often inefficient conventional microbial recovery methods. ?
The presence of bromide in drinking water typically leads to the formation of brominated DBPs upon chlorination. Bromide is not removed by conventional water treatment processes. Ion-exchange and high-pressure membrane filtration remove bromide but produce a concentrated brine waste stream. One emerging technology for bromide removal is electrolysis. Limited design data on bromide removal by electrolysis are available in the literature. However, design parameters, operational constraints, and costs need to be defined. The objectives of the study were to (1) determine operational conditions under which electrolysis removes bromide and decreases the formation of halogenated disinfection by-products (DBPs); (2) investigate the effect of electrolysis on ozonation DBPs (bromate), bacterial regrowth, and taste andor; (3) evaluate the impact of electrolysis on conventional coagulation/flocculation/sedimentation and ozonation; (4) evaluate scalability and conceptual design issues; (5) determine preliminary capital and operational costs; and (6) determine future needs for demonstrating the technology. A four phased-approach was undertaken to conduct this project. During the first phase, the electrolytic reactor was designed, constructed, and activated. During the second phase, the electrolytic reactor was operated under several conditions of hydraulic residence time, current level, and influent bromide level. Key analytical parameters were measured, including bromide, bromine, chlorine, and THM and HAA concentrations. During the third phase, conventional treatment consisting of coagulation/flocculation/sedimentation and/or ozonation was tested downstream of electrolysis to investigate whether electrolysis is feasible in a conventional treatment plant context. During the fourth phase, scale up, safety, and conceptual design issues were identified and preliminary costs estimated. A workshop was held towards the end of the study to identify future needs.
Microbial contamination of drinking water and waterborne disease outbreaks continue to present a significant concern for the water industry. There is a need for pathogen detection methods that (1) incorporate sensitive detection and identification at the species/strain level, (2) have the ability to process many samples simultaneously, (3) involve minimal risk of false identification, (4) are adaptable, and (5) contain the capacity for some degree of automation. Molecular-based assays in high-throughput multi-well formats meet these requirements.? The demonstration of the feasibility of a microplate-based rapid screening assay indicates that the water industry should continue to pursue and fund exploratory research into the development of innovative pathogen detection methods. Such techniques may be used for routine screening of drinking water during outbreak situations, or to investigate episodes of intentional contamination. All of these situations require pathogen detection tools that can generate results, even if the results are only presumptive, in as short a time as possible. The assay may be linked to direct nucleic extraction methods so that all potential pathogens can be screened in a sample, thereby uncoupling the assay from time-consuming and often inefficient conventional microbial recovery methods. ?