Appendix 2.2 PRACTICAL GUIDANCE ON THE DESIGN AND VERIFICATION OF UV DISINFECTION SYSTEMS TARGETED GOALS OF UV SYSTEM
Promote an understanding of system goals, determined by the system
designer, following a DWSP approach to the hazard control involving; The assessment of catchment and source risks with respect to the clarity, organic content, and the likely risk of pathogenic micro-organisms in the source water The evaluation of particular source risk following analysis of raw water sampling to determine the extent of pathogen inactivation required of the UV disinfection system The determination of the pre-treatment process(es), necessary to ensure the required clarity of the water (with respect to colour, turbidity and TOC) and/or inorganic chemical removal, upstream of the chosen reactor The goals of the chosen UV system, whether as the primary disinfectant or as part of a multi-barrier approach, to achieve the target pathogen inactivation levels established with respect to bacteria, viruses and protozoa. DECISION FLOWCHART TREATED WATER CLARITY AND INSTALLATION CONSTRAINTS REACTOR GOALS, DOSE CONTROL STRATEGY AND MONITORING SYSTEM VALIDATION
Validation certification sets out the UV reactor capability to
apply a UV dose and deliver the targeted inactivation of pathogens under defined operating conditions: – the range of flow rates through the reactor(s) – the clarity of the water, as per the minimum UVT established by a sampling regime for the water – the measured UV intensity transmitted through the water as it passes through the reactor – pipe installation criteria associated with the validation test – the maximum number of hours since the lamps were last replaced SYSTEM VALIDATION Dose Monitoring Strategies – UV Setpoint Intensity Approach - ONORM and DVGW (Small systems) – UV intensity which alters dose in response to changes in flow rate and lamp aging – UVT monitoring is not needed to confirm dose delivery – Calculated Dose Approach – USEPA (Large systems) – UV dose is calculated using an equation dependent on flow rate, UV intensity, UVT and lamp status. The measured UV intensity sets the lamp power to sustain the required dose in reply to varying flow and UVT – The dosing of UV to achieve different log inactivation values and the specific targeting of pathogens as part of a multi-barrier approach to drinking water disinfection can be better accommodated – Approach enables UV dose pacing, which reduces operating costs and allows more energy efficient operation of larger UV reactor systems when water quality and flow rate varies REQUIREMENTS FOR SYSTEM OPERATION AND VERIFICATION Guidance for plant operators in the operation of a UV disinfection system; Understanding of the target goals of the UV system to be operated Knowledge of the capability of the UV reactor(s) in operation, as determined by the validation certification of the particular reactor(s), including the dose monitoring strategy on which the certification is based knowledge of the functionality of the various elements of the reactor(s) and the associated instrumentation for the monitoring of key parameters to ensure correct UV system operation in accordance with its validation ensure that the pipe manifold on which UV reactors are installed remain full of water when flow through the system decreases to zero. REQUIREMENTS FOR SYSTEM OPERATION AND VERIFICATION Guidance for plant operators in the verification of a UV disinfection system operation; Need for records to show that – UV system is operated and maintained as per the validation certification i.e. flow, UVI, UV Dose and UVT (as required) – History of alarm generation – lamps and other components are replaced after stipulated maximum usage periods – associated monitoring instrumentation are calibrated and where necessary replaced at the frequency stipulated in the validation standards and in the manufacturers instructions TYPICAL ALARM GENERATION
ALARM SETPOINT ALARM TYPE PURPOSE
Lamp Age Minor alarm Run-time indicating end of defined operational lamp life Calibration of UV sensor Minor alarm UV sensor requiring calibration check based on operating time. Low UV Validated Dose Major alarm Indicated validated UV dose (based on reactor parameters, i.e., flow, UVI, and UVT) falls below required UV dose (USEPA) Low UV Intensity Major alarm Intensity falls below validated conditions (DVGW /ONORM) Low UVT Major alarm UVT falls below validated conditions (USEPA) High Flow Major alarm Flow rate falls outside of validated range Mechanical Wiper Failure Major alarm Lamp wipe function fails Lamp Ballast failure Major alarm Single lamp/ballast failure identified Critical alarm Multiple lamp/ballast failures identified. Low Liquid Level Critical alarm Liquid level within the UV reactor drops and potential for overheating increases. High Temperature Critical alarm Temperature within the UV reactor or ballast >setpoint MONITORING OF UV SYSTEM OPERATION The following are required to facilitate verification of UV disinfection as per Clause 12.1 of the Drinking Water Regulations (SI 278 of 2007) Validation certification by bioassay testing of all UV reactors used The monitoring and reporting of system performance Recording of flow, lamp status and UVI at 4 hour intervals Monthly calibration of duty UV sensor using reference sensor i.e. |UVI duty (%) − UVI reference( %)| < 20% Weekly calibration of UVT analyser (only if part of dose monitoring strategy) (USEPA) i.e. |UVTon - line (%) − UVTbench( %)| < 2% Recording of the following off-specification events & the monthly off-specification volume which should be < 5% of the total volume e.g. Flow > validated flow or UVT < validated UVT or Validated dose < Required dose for target pathogen inactivation SAMPLE DAILY LOG FOR UV SYSTEM VERIFICATION From Appendix 2.4 SAMPLE DAILY LOG FOR UV SYSTEM VERIFICATION From Appendix 2.4