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Australian Drinking Water Guidelines
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  • Australian Drinking Water Guidelines
  • Copyright
  • Table of updates
  • Contents
  • Figures
  • Tables
  • Boxes
  • Introduction
    • Chapter 1: Introduction
      • 1.1 Guiding principles
      • 1.2 About the Guidelines
        • 1.2.1 Scope of the Guidelines
        • 1.2.2 Purpose of the Guidelines
        • 1.2.3 Structure of the Guidelines
      • 1.3 Water quality characteristics
        • 1.3.1 Introduction
        • 1.3.2 Health-based targets
        • 1.3.3 Microbial health-based targets
        • 1.3.4 Physical and chemical guideline values
        • 1.3.5 Radiological screening and reference values
      • 1.4 Community consultation
      • 1.5 Development of the Guidelines
        • 1.5.1 Acknowledgments
      • 1.6 Future revisions of the Guidelines
      • 1.7 References
  • Part 1: Management of Drinking Water Quality
    • Chapter 2: Framework for Management of Drinking Water Quality: overview
      • 2.1 A preventive strategy from catchment to consumer
      • 2.2 Structure of the Framework
      • 2.3 Benefits of the Framework
      • 2.4 The need for multi-agency involvement
      • 2.5 Applying the Framework
      • 2.6 Correlations of the Framework with other systems
    • Chapter 3: Framework for Management of Drinking Water Quality: the twelve elements
      • 3.1 Commitment to drinking water quality management (element 1)
        • 3.1.1 Drinking water quality policy
        • 3.1.2 Regulatory and formal requirements
        • 3.1.3 Engaging stakeholders
      • 3.2 Assessment of the drinking water supply system (element 2)
        • 3.2.1 Water supply system analysis
        • 3.2.2 Assessment of water quality data
        • 3.2.3 Hazard identification and risk assessment
      • 3.3 Preventive measures for drinking water quality management (element 3)
        • 3.3.1 Preventive measures and multiple barriers
        • 3.3.2 Critical control points
      • 3.4 Operational procedures and process control (element 4)
        • 3.4.1 Operational procedures
        • 3.4.2 Operational monitoring
        • 3.4.3 Corrective action
        • 3.4.4 Equipment capability and maintenance
        • 3.4.5 Materials and chemicals
      • 3.5 Verification of drinking water quality (element 5)
        • 3.5.1 Drinking water quality monitoring
        • 3.5.2 Consumer satisfaction
        • 3.5.3 Short-term evaluation of results
        • 3.5.4 Corrective action
      • 3.6 Management of incidents and emergencies (element 6)
        • 3.6.1 Communication
        • 3.6.2 Incident and emergency response protocols
      • 3.7 Employee awareness and training (element 7)
        • 3.7.1 Employee awareness and involvement
        • 3.7.2 Employee training
      • 3.8 Community involvement and awareness (element 8)
        • 3.8.1 Community consultation
        • 3.8.2 Communication
      • 3.9 Research and development (element 9)
        • 3.9.1 Investigative studies and research monitoring
        • 3.9.2 Validation of processes
        • 3.9.3 Design of equipment
      • 3.10 Documentation and reporting (element 10)
        • 3.10.1 Management of documentation and records
        • 3.10.2 Reporting
      • 3.11 Evaluation and audit (element 11)
        • 3.11.1 Long-term evaluation of results
        • 3.11.2 Audit of drinking water quality management
      • 3.12 Review and continual improvement (element 12)
        • 3.12.1 Review by senior executive
        • 3.12.2 Drinking water quality management improvement plan
      • 3.13 References
    • Chapter 4: Framework for the Management of Drinking Water Quality: application to small water supplies
      • 4.1 Introduction
      • 4.2 Applying the Framework
        • 4.2.1 Assessment of the drinking water supply
        • 4.2.2 Preventive measures for drinking water quality management
        • 4.2.3 Implementation of operational procedures and process control
        • 4.2.4 Verification of drinking water quality
      • 4.3 Individual household supplies
      • 4.4 Reference
  • Part 2: Description of Water Quality
    • Chapter 5: Microbial Quality of Drinking Water (Updated 2022)
      • 5.1 Introduction
      • 5.2 Microorganisms in drinking water
      • 5.3 Assessing microbial risk
      • 5.4 Enteric pathogens
        • 5.4.1 Enteric pathogens of concern in drinking water
        • 5.4.2 Contamination of source waters with enteric pathogens
        • 5.4.3 Management of risk from enteric pathogens
      • 5.5 Opportunistic pathogens
      • 5.6 Cyanobacteria
      • 5.7 Nuisance organisms
        • 5.7.1 Organisms causing taste and odour problems
        • 5.7.2 Organisms causing colour problems
        • 5.7.3 Deposits due to iron and manganese bacteria
        • 5.7.4 Corrosion problems due to iron and sulphur bacteria
        • 5.7.5 Problems caused by large numbers of microorganisms
      • 5.8 References
    • Chapter 6: Physical and Chemical Quality of Drinking Water
      • 6.1 Introduction
      • 6.2 Physical quality of drinking water
        • 6.2.1 An overview of physical characteristics
        • 6.2.2 Approach used in derivation of guidelines values for physical characteristics
      • 6.3 Chemical quality of drinking water
        • 6.3.1 Inorganic chemicals
        • 6.3.2 Organic compounds (Revised 2011)
        • 6.3.3 Approach used in derivation of guideline values for chemicals
      • 6.4 Differences between Australian and WHO guideline values
      • 6.5 National and international guideline values (2016)
      • 6.6 References
    • Chapter 7: Radiological Quality of Drinking Water (Updated 2022)
      • 7.1 Introduction
      • 7.2 Sources of radiation in the environment and in drinking water
      • 7.3 Health effects of radiation
      • 7.4 Exposure to radiation
      • 7.5 Units of radioactivity and radiation dose measurement
        • 7.5.1 Units of radioactivity and radiation dose
        • 7.5.2 Converting intake to radiation dose
        • 7.5.3 Average dose of radiation
      • 7.6 Approach for derivation of reference levels and screening values for radionuclides
        • 7.6.1 System for radiation protection
        • 7.6.2 Estimation of the dose from radionuclides in water
        • 7.6.3 Estimation of risk from low-level radiation
        • 7.6.4 Reference levels and screening values for drinking water
        • 7.6.5 Application of reference levels
        • 7.6.6 Remedial measures
      • 7.7 References
    • Chapter 8: Drinking Water Treatment Chemicals (Revised 2006)
      • 8.1 Introduction
      • 8.2 Scope and limit of application of this chapter
      • 8.3 Overview of chemical treatment processes
        • 8.3.1 Control of algae
        • 8.3.2 Coagulation and flocculation
        • 8.3.3 Adsorption
        • 8.3.4 Softening
        • 8.3.5 Oxidation
        • 8.3.6 Disinfection
        • 8.3.7 Adjustment of pH
        • 8.3.8 Addition of buffering capacity
        • 8.3.9 Corrosion inhibition
      • 8.4 Public health measures
        • 8.4.1 Fluoridation
      • 8.5 Assessment of Chemicals acceptable for use in drinking water treatment (revised 2016)
        • 8.5.1 Chemicals assessed prior to 2004
        • 8.5.2 New water treatment chemicals
      • 8.6 Quality assurance for drinking water treatment chemicals
        • 8.6.1 Risks associated with drinking water chemicals
        • 8.6.2 Managing risks
        • 8.6.3 Specifications for the supply of drinking water treatment chemicals
      • 8.7 Monitoring and analytical requirements
      • 8.8 Contaminants in drinking water treatment chemicals
      • 8.9 Useful contacts
      • 8.10 References
  • Part 3: Monitoring
    • Chapter 9: Overview of monitoring (Revised 2021)
      • 9.1 Introduction
      • 9.2 Monitoring overview
        • 9.2.1 Monitoring priorities
        • 9.2.2 Principles of monitoring frequency
        • 9.2.3 Catchment-to-consumer monitoring
      • 9.3 Developing a monitoring program
      • 9.4 Operational monitoring
        • 9.4.1 Operational characteristics
        • 9.4.2 Target criteria
        • 9.4.3 Critical limits at critical control points
        • 9.4.4 Corrective action
        • 9.4.5 Operational monitoring frequency
        • 9.4.6 Chlorination as a critical control point: an example
      • 9.5 Verification of drinking water quality
        • 9.5.1 Monitoring consumer satisfaction
        • 9.5.2 Drinking water quality monitoring
      • 9.6 Water quality issues beyond the point of supply
      • 9.7 Investigative studies and research monitoring
      • 9.8 Validation of barrier performance
      • 9.9 Incident and emergency response monitoring
      • 9.10 Reliability of monitoring data
        • 9.10.1 Sample integrity
        • 9.10.2 Methods
        • 9.10.3 Detection limits
        • 9.10.4 Measurement uncertainty
        • 9.10.5 Field testing
      • 9.11 Monitoring advice for small, remote or community-managed water supplies
      • 9.12 Assessing the significance of short-term exceedances of health-based guideline values
      • 9.13 References
    • Chapter 10: Monitoring for specic characteristics in drinking water (Updated 2022)
      • 10.1 Introduction
      • 10.2 Assessing safety: short-term evaluation of monitoring
        • 10.2.1 Short-term evaluation of operational monitoring
        • 10.2.2 Short-term evaluation of drinking water quality monitoring
      • 10.3 Assessing performance: long-term evaluation of monitoring
        • 10.3.1 Long-term evaluation of microbial performance
        • 10.3.2 Long-term evaluation of health-based chemical performance
        • 10.3.3 Long-term evaluation of aesthetic performance
        • 10.3.4 Long-term evaluation of consumer satisfaction
        • 10.3.5 Improvement plan
        • 10.3.6 Performance reporting
        • 10.3.7 Summary of guideline values for microbial, chemical and physical characteristics
        • 10.3.8 Summary of reference levels and screening values for radiological characteristics
      • 10.4 Reference
  • Part 4: Information sheets
    • 1. Disinfection
      • 1.1: Introduction to water treatment
      • 1.2: Overview of disinfection
      • 1.3: Disinfection with chlorine
      • 1.4: Chloramines
      • 1.5: Disinfection with chlorine dioxide
      • 1.6: Disinfection with ozone
      • 1.7: Disinfection with ultraviolet light
      • 1.8: Other disinfectants
    • 2. Sampling
      • 2.1: Sampling Information – handling requirements and preservation
      • 2.2: Radiological monitoring and assessment of performance (updated 2022)
    • 3. Statistics
      • 3.1: Statistics – Visualising data
      • 3.2: Statistics – Assessing data
      • 3.3: Statistics – Statistical principles
      • 3.4: Statistics – Control charts and trends
      • 3.5: Number of samples required
      • 3.6: Guidance for issuing and lifting boil water advisories
      • Attachments
  • Part 5: Fact sheets
    • Microorganisms
      • Microbial indicators
        • Bacteroides
        • Coliphages
        • Clostridium perfringens
        • Escherichia coli
        • Heterotrophic plate counts
        • Intestinal enterococci
        • Thermotolerant coliforms
        • Total coliforms
      • Bacteria
        • Aeromonas
        • Burkholderia pseudomallei
        • Campylobacter
        • Escherichia coli (E. coli) (pathogenic)
        • Helicobacter pylori
        • Klebsiella
        • Legionella
        • Mycobacterium
        • Pseudomonas aeruginosa
        • Salmonella
        • Shigella
        • Vibrio
        • Yersinia
      • Protozoa
        • Acanthamoeba
        • Blastocystis
        • Cryptosporidium
        • Cyclospora
        • Giardia
        • Naegleria fowleri
      • Cyanobacteria and their toxins
        • Cyanobacteria and their toxins
        • Cylindrospermopsin
        • Microcystins
        • Nodularin
        • Saxitoxins
      • Viruses
        • Adenovirus
        • Enterovirus
        • Hepatitis viruses
        • Norovirus
        • Rotavirus
    • Physical and chemical characteristics
      • Acephate
      • Acrylamide
      • Aldicarb
      • Aldrin and Dieldrin
      • Aluminium
      • Ametryn
      • Amitraz
      • Amitrole
      • Ammonia
      • Antimony
      • Arsenic
      • Asbestos
      • Asulam
      • Atrazine
      • Azinphos-methyl
      • Barium
      • Benomyl
      • Bentazone
      • Benzene
      • Beryllium
      • Bioresmethrin
      • Boron
      • Bromacil
      • Bromate
      • Bromoxynil
      • Cadmium
      • Captan
      • Carbaryl
      • Carbendazim/Thiophanate-methyl
      • Carbofuran
      • Carbon tetrachloride
      • Carboxin
      • Carfentrazone-ethyl
      • Chloral hydrate (Trichloroacetaldehyde)
      • Chlorantraniliprole
      • Chlordane
      • Chlorfenvinphos
      • Chloride
      • Chlorinated furanones
      • Chlorine
      • Chlorine dioxide, Chlorite, Chlorate
      • Chloroacetic acids: chloroacetic acid, dichloroacetic acid (DCA), trichloroacetic acid (TCA)
      • Chlorobenzene
      • Chloroketones
      • Chlorophenols
      • Chloropicrin
      • Chlorothalonil
      • Chlorpyrifos
      • Chlorsulfuron
      • Chromium
      • Clopyralid
      • Colour (True)
      • Copper
      • Cyanide
      • Cyanogen chloride
      • Cyfluthrin, Beta-cyfluthrin
      • Cypermethrin isomers
      • Cyprodinil
      • 2,4-D [(2,4-Dichlorophenoxy) acetic acid]
      • DDT (1,1,1-trichloro-di-(4-chlorophenyl) ethane)
      • Deltamethrin
      • Diazinon
      • Dicamba
      • Dichlorobenzenes
      • Dichloroethanes: 1,1-dichloroethane, 1,2-dichloroethane
      • Dichloroethenes: 1,1-dichloroethene (1,1-DCE), 1,2-dichloroethene (1,2-DCE)
      • Dichloromethane (methylene chloride)
      • 1,3-Dichloropropene
      • Dichlorprop/Dichlorprop-P
      • Dichlorvos
      • Diclofop-methyl
      • Dicofol
      • Diflubenzuron
      • Dimethoate
      • Diquat (ion), Diquat dibromide
      • Dissolved oxygen
      • Disulfoton
      • Diuron
      • 2,2-DPA
      • Endosulfan
      • Endothal
      • Epichlorohydrin
      • EPTC
      • Esfenvalerate
      • Ethion
      • Ethoprophos
      • Ethylbenzene
      • Ethylenediamine tetraacetic acid (EDTA)
      • Etridiazole
      • Fenamiphos
      • Fenarimol
      • Fenchlorphos
      • Fenitrothion
      • Fenthion
      • Fenvalerate
      • Fipronil
      • Flamprop-methyl
      • Fluometuron
      • Fluoride
      • Flupropanate
      • Formaldehyde
      • Glyphosate
      • Haloacetonitriles
      • Haloxyfop
      • Hardness (as calcium carbonate)
      • Heptachlor and heptachlor epoxide
      • Hexachlorobutadiene
      • Hexazinone
      • Hydrogen sulfide, Sulfide
      • Imazapyr
      • Iodine, Iodide
      • Iprodione
      • Iron
      • Lanthanum
      • Lead
      • Lindane
      • Maldison (Malathion)
      • Mancozeb
      • Manganese
      • MCPA
      • Mercury
      • Metaldehyde
      • Metham
      • Methidathion
      • Methiocarb
      • Methomyl
      • Methyl bromide
      • Metiram
      • Metolachlor/s-Metolachlor
      • Metribuzin
      • Metsulfuron-methyl
      • Mevinphos
      • Molinate
      • Molybdenum
      • Monochloramine
      • Naphthalophos
      • Napropamide
      • Nicarbazin
      • Nickel
      • Nitrate and nitrite
      • Nitrilotriacetic acid (NTA)
      • N-Nitrosodimethylamine (NDMA)
      • Norflurazon
      • Omethoate
      • Organotins: dialkyltins, tributyltin oxide
      • Oryzalin
      • Oxamyl
      • Paraquat
      • Parathion
      • Parathion-methyl
      • Pebulate
      • Pendimethalin
      • Pentachlorophenol
      • Per-fluoroalkyl and poly-fluoroalkyl substances (PFAS)
      • Permethrin
      • pH
      • Picloram
      • Piperonyl butoxide
      • Pirimicarb
      • Pirimiphos methyl
      • Plasticisers
      • Polihexanide
      • Polycyclic aromatic hydrocarbons (PAHs)
      • Profenofos
      • Promecarb
      • Propachlor
      • Propanil
      • Propargite
      • Propazine
      • Propiconazole
      • Propyzamide
      • Pyrasulfotole
      • Pyrazophos
      • Pyroxsulam
      • Quintozene
      • Radionuclides, Specific Alpha and Beta Emitting
      • Radium (radium-226 and radium-228)
      • Radon-222
      • Selenium
      • Silica
      • Silver
      • Simazine
      • Sodium
      • Spirotetramat
      • Styrene (vinylbenzene)
      • Sulfate
      • Sulprofos
      • Taste and Odour
      • Temephos
      • Temperature
      • Terbacil
      • Terbufos
      • Terbuthylazine
      • Terbutryn
      • Tetrachloroethene
      • Thiobencarb
      • Thiometon
      • Thiram
      • Tin
      • Toltrazuril
      • Toluene
      • Total dissolved solids
      • Triadimefon
      • Trichlorfon
      • Trichlorobenzenes
      • 1,1,1-Trichloroethane
      • Trichloroethylene (TCE)
      • Triclopyr
      • Trifluralin
      • Trihalomethanes (THMs)
      • Turbidity
      • Uranium
      • Vernolate
      • Vinyl chloride
      • Xylenes
      • Zinc
    • Drinking water treatment chemicals
      • Aluminium chlorohydrate
      • Aluminium sulfate (alum)
      • Ammonia
      • Ammonium sulfate
      • Calcium hydroxide
      • Calcium hypochlorite
      • Calcium oxide
      • Carbon, granulated activated
      • Carbon, powdered activated
      • Chlorine
      • Copper sulfate
      • Ferric chloride
      • Ferric sulfate
      • Hydrochloric acid
      • Hydrofluorosilicic acid
      • Hydrogen peroxide
      • Hydroxylated ferric sulfate
      • Ozone
      • Polyacrylamide
      • Polyaluminium chloride
      • Polyaluminium silica sulfates
      • Polydiallyldimethylammonium chloride
      • Potassium permanganate
      • Sodium aluminate
      • Sodium bicarbonate
      • Sodium carbonate
      • Sodium fluoride
      • Sodium fluorosilicate
      • Sodium hexametaphosphate
      • Sodium hydroxide
      • Sodium hypochlorite
      • Sodium silicate
      • Sodium tripolyphosphate
      • Sulfuric acid
      • Zinc orthophosphate
  • Appendices
    • Appendix 1: Additional guidance
      • A1.1 Introduction
      • A1.2 Water supply system analysis
      • A1.3 Assessment of water quality data
      • A1.4 Hazard identification
      • A1.5 Risk assessment
      • A1.6 Preventive measures and multiple barriers
      • A1.7 Critical control points
      • A1.8 Chlorination as an example of a critical control point
      • A1.9 References
    • Appendix 2: Further sources of information on drinking water quality management
      • A2.1 Drinking water quality management - general
      • A2.2 Catchment management and source water protection
      • A2.3 Groundwater protection
      • A2.4 Risk assessment and management
      • A2.5 System analysis and management process control and optimisation
      • A2.6 Monitoring and verification
      • A2.7 Materials and chemicals
      • A2.8 Incident and emergency management
      • A2.9 Employee training and awareness
      • A2.10 Research and development
      • A2.11 Documentation and reporting
      • A2.12 Community consultation and communication
      • A2.13 Hazard analysis and critical control point (HACCP)
      • A2.14 Quality management continuous improvement
      • A2.15 Reference web sites
    • Appendix 3: Derivation of microbial treatment targets for enteric pathogens
      • A3.1 Introduction to Quantitative Microbial Risk Assessment (QMRA)
      • A3.2 Adopting the QMRA approach in the Guidelines
      • A3.3 QMRA framework for the calculation of log₁₀ reduction values (LRVs)
      • A3.4 Defining the health outcome target
      • A3.5 Selection of reference pathogens
      • A3.6 Level of reference pathogen contamination in Australian source waters
      • A3.7 Consumption volume of unheated (unboiled) water per person per day
      • A3.8 Dose response relationships
      • A3.9 Disability Adjusted Life Years (DALY) burden per case
      • A3.10 Calculation of LRVs using the QMRA framework
      • A3.11 Interpretation of calculated LRVs for practical treatment guidance
      • A3.12 Understanding log₁₀ reductions
      • A3.13 References
  • Glossary
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Australian Drinking Water Guidelines 6 2011, v3.9

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On this page
  • Properties of an ideal disinfectant
  • Effectiveness of Disinfection
  • Table IS1.2.1 Applicability of disinfection techniques to different situations
  • Factors affecting disinfection
  • Disinfection and residual management
  • Managing water supplies with no residual
  • References
  1. Part 4: Information sheets
  2. 1. Disinfection

1.2: Overview of disinfection

Disinfection of public water supplies commenced early in the 20th century and together with filtration is credited with substantial reductions in waterborne disease (Cutler and Miller 2005, CDC 1999). Most Australian public water supplies are disinfected and it is recognised as a fundamental barrier to microbial contamination.

Disinfection may be practiced alone in circumstances where the source water is of a high quality or as the final step in a water treatment process that utilises multiple barriers. The decision to use disinfection alone, or in combination with other water treatment processes, is determined by a system-specific risk assessment, which includes an assessment of the quality of the source water. In most cases disinfection will be used as part of a multiple barrier approach to the production of safe drinking water.

In all cases disinfection should be treated as a critical control point (CCP) (see section 3.3.2 for more information on CCPs). This means the failure of the disinfection process may lead to the water being unsafe to drink.

Common agents used to disinfect water include chlorine, chloramine, chlorine dioxide, ozone and ultra violet (UV) light. Information sheets 1.3 - 1.7 describe these disinfectants. This information sheet on disinfection should be read in conjunction with the relevant fact sheets for each disinfectant, which discuss the chemical by-products produced by each disinfectant.

Properties of an ideal disinfectant

An ideal disinfectant should:

  • Effectively inactivate pathogenic micro-organisms over a wide range of physical and chemical conditions;

  • Be able to have its efficacy continuously monitored;

  • Provide ongoing protection from pathogenic micro-organisms that may be introduced into the distribution system;

  • Provide a disinfectant residual that is stable and easily measured in the field;

  • Produce minimal levels of by-products;

  • Be readily available, safe to handle and suitable for widespread use;

  • Not degrade in quality or strength during storage; and

  • Be affordable (in terms of both capital and operating costs).

No single disinfectant currently meets all these criteria. Despite the limitations, disinfectants are an essential step and widely used in the production of safe drinking water. Choosing the appropriate disinfectant is an important decision for effective drinking water quality management in any water supply system. Factors which influence that decision include:

  • The quality of the source water being treated including:

    • The type of micro-organisms present (e.g. pathogenic bacteria, viruses, and/or protozoa)

    • The type and concentration of organic matter present in the source water

    • Propensity of the source water to form disinfection by-products

    • Turbidity, colour, UV absorbance, pH, alkalinity and water temperature (i.e., factors that affect disinfectant effectiveness)

  • The characteristics of the water supply system including:

    • Volume and dose rate of disinfectant required to maintain effective disinfection

    • The type and concentration of organic matter present in the treated water

    • Propensity of the treated water to form disinfection by-products

    • Retention time within the distribution system

    • Pipe condition

    • Size and complexity of the distribution system

  • Specific local circumstances such as:

    • Personnel safety

    • Public safety

    • Supply logistics

    • Technical capacity of staff to operate the disinfection facility

    • Technical support for operators to operate and maintain the disinfection facility

    • Cost

Effectiveness of Disinfection

Determining the effectiveness of chemical disinfectants

The C.t concept describes the relative effectiveness of a specific aqueous disinfectant against different microorganisms under specified conditions. It is determined by multiplying the concentration or residual of the disinfectant (in mg/L) by the contact time (in minutes). The C.t concept is expressed mathematically as:

where:

k = Cn.t

C = concentration of residual disinfectant

n = constant (also called the coefficient of dilution)

t = contact time required for a fixed per cent of inactivation

k= constant for a specific microorganism exposed under set conditions.

Reported values for “n” range from 0.5 to 1.8 for most aqueous disinfectants. Generally, however, “n” approximates 1, and the equation is simplified to k = C.t.

C.t values for specific organisms exposed to particular disinfectants can be calculated. A low C.t value indicates a strong primary disinfectant.

Comparative effectiveness of disinfection, based on the C.t concept, for the four major disinfectants for a range of micro-organisms, are given in Information Sheets 1.3 to 1.6. The figures presented represent published C.t values that achieve 99% (or 2 log) inactivation of the target microorganism. In summary, the published C.t values show that ozone and chlorine dioxide are very effective at inactivating most microorganisms. Chlorine is effective at inactivating bacteria and viruses, but is less effective against Giardia, and not effective at inactivating Cryptosporidium at a C.t value that could be applied to a drinking water supply. Chloramine requires a considerably higher C.t value than chlorine to inactivate bacteria and viruses; it is ineffective against Cryptosporidium and Giardia at C.t values that could be applied to a drinking water supply.

The relative merits of various disinfectants, and ultraviolet light (UV), are summarised in Table IS1.2.1.

Table IS1.2.1 Applicability of disinfection techniques to different situations

Consideration
Chlorine
Chloramination
Ozone
Chlorine dioxide
Ultraviolet light

Relative complexity of technology

Simple to Moderate

Simple to Moderate

Complex

Moderate

Simple to Moderate

Safety Concerns

Yes

Yes

Yes

Yes

Minimal

Bactericidal

Good

Good

Good

Good

Good

Virucidal

Moderate

Poor

Good

Good

Good

Protozocidal

Poor

Poor

Good

Moderate

Good

By-products of possible health concern

Yes

Yes

Yes

Yes

No

Persistent residual

Moderate

Long

None

Moderate

None

Contact Time

Moderate

Long

Short

Moderate

Short

pH dependent

Yes

Yes

Slightly

Slightly

No

Process control

Well developed

Well developed

Developed

Developed

Well developed

Where contact tanks or clear water storages are used to achieve the desired contact time, the T₁₀ contact time needs to be taken into consideration (Church and Colton 2013; USEPA 2003). The T₁₀ contact time is the minimum detention time experienced by 90 percent of the water passing through the tank, and is based on a baffling factor or tracer studies (Church and Colton 2013).

Determining the effectiveness of ultraviolet disinfection

The C.t concept does not apply to UV disinfection. UV disinfection relies on exposure of pathogens to UV irradiation, measured as UV fluence or UV dose, in mJ/cm2\text{mJ/cm}^2mJ/cm2. Different pathogens respond differently to UV irradiation so the target UV dose is typically selected based on the main pathogen/s of concern for a given source water.

The UV dose achieved by a given unit is a function of the following:

  • UV transmittance (UVT %), i.e. water quality;

  • lamp power (Watts); and

  • exposure time (which is typically related to flow rate).

Wherever possible, a validated UV system should be used, and preferably those systems that have been validated in accordance with the requirements of the USEPA Ultraviolet disinfection guidance manual for the final long term 2 enhanced surface water treatment rule (UVDGM) (2006). Other validation processes for UV systems also exist (DVGW, 2006a, 2006b, 2006c; ONORM, 2001, 2003; and NWRI, 2012).

The monitoring, operation and maintenance requirements that must be applied to ensure the ongoing performance of the UV unit at the required dose, as detailed in USEPA UV Disinfection Guidance Manual (2006) include:

  • flow, UVT and lamp power set points;

  • maintenance and calibration of essential UVT or UV intensity instrumentation; and

  • UV lamp monitoring, cleaning and replacement.

Finally, it should be recognised that energy consumption is a significant contributor to operating cost for UV disinfection systems, particularly large scale systems. Consequently, the accurate and efficient setting and control of the UV dose is important to avoid any undue overdose and therefore energy wastage.

Ensuring the effectiveness of disinfection

As one of the most important processes in assuring safe drinking water, disinfection will always be a CCP (see section 3.3.2). This means the disinfection process should be continuously monitored to provide assurance that it is functioning correctly (see Appendices A1.7 and A1.8).

For chlorination, chloramination and chlorine dioxide this is best achieved by permanent online chlorine residual analysers installed downstream of disinfection.

With disinfection processes that do not provide a residual, other parameters can be monitored to confirm disinfection effectiveness, e.g. the intensity of UV dose can be monitored for UV performance. A key consideration is ensuring that effective disinfection is achieved under the most extreme operating conditions of maximum flows and minimum detention times.

Given that disinfection will be a CCP, other important issues that will need to be considered to ensure the effectiveness of the disinfection process are:

  • establishing target criteria and critical limits for the disinfection process (section 3.4.2);

  • preparing and implementing operational procedures (section 3.4.1) and operational monitoring (section 3.4.2) for the process;

  • preparing corrective action procedures (section 3.4.3) in the event that there are excursions in the operational parameters; and

  • undertaking employee training (section 3.7.2) to ensure that the treatment process operates to the established target criteria and critical limits.

It is important to note that when chlorine, chloramine, ozone and chlorine dioxide are used as disinfectants, if the disinfectant comes into contact with organic matter a range of disinfection by-products (DBP) can be formed. The by-products produced by individual disinfectants, and their potential health significance, are described in the Fact Sheets for each disinfectant.

It is also important to note that the possible presence of microbial contaminants in drinking water poses a greater risk to public health than the possible presence of DBP. Therefore, disinfection should not be compromised in order to control DBP.

Factors affecting disinfection

Disinfection processes, and their associated C.t values, are affected by a range of external factors, such as the pH and temperature of the water. Particle shielding can also reduce disinfection.

Water quality operators and managers need to understand the factors which can adversely impact on effectiveness of the disinfection process and monitor these parameters, in order to achieve effective disinfection.

The table below summarises the parameters which might impact on the effectiveness of disinfection which should be monitored for common disinfectants.

Disinfectant Parameters which may impact the effectiveness of disinfectants

Chlorine

Turbidity, pH, temperature

Chloramine

Turbidity, pH, temperature

Chlorine dioxide

Turbidity, pH, temperature

Ozone

Turbidity, pH, temperature

Ultraviolet irradiation

Turbidity, colour, iron and UV absorbance or UV transmissivity (UVT)

Ideally these parameters should be monitored continuously, especially for source waters where water quality can change rapidly. If source waters are very stable (such as confined groundwater) it may be acceptable to monitor with regular grab samples.

The table above does not include all the operational parameters which should be monitored to demonstrate the effectiveness of disinfection process. Further details can be found in the Information Sheet for each disinfectant.

If the target criterion for an operational parameter is breached, it does not necessarily mean that disinfection has been compromised. In such instances the water utility needs to:

  • Validate that disinfection is still effective, specifically in the circumstance where supply has to be maintained during the period that the operational parameter is outside the target range;

  • Where possible, use an alternative source water;

  • Where possible, only take raw water that is within, or has returned to within, the target range for the water treatment processes that are being used; and

  • Verify that the water within the distribution system is still of a satisfactory quality.

Disinfection and residual management

When operating a distribution system it is important to understand the difference between effective disinfection and maintaining a disinfectant residual. The water is effectively disinfected when the required C.t value has been achieved. After effective disinfection, enteric pathogens should not reappear within the distribution system, unless there is a failure in the integrity of the system. Therefore, unless there is a barrier breach within the distribution system the water should remain safe to drink even in the absence of adequate disinfectant residual. Barrier breaches could include such things as ingress, backflow, loss of pressure within the distribution system, or contamination within post-treatment storage tanks.

Operationally, a sudden loss of chlorine residual within the distribution system can also warn of an unusual event or potential contamination, such as backflow, within the distribution system.

Most Australian water utilities use chlorine as their disinfectant of choice with C.t target of at least 15 mg/L.min which is consistent with the World Health Organization’s recommendation that effective disinfection can generally be achieved by maintaining a free chlorine concentration of 0.5 mg/L for 30 minutes (WHO, 2011). Based on data contained in Information Sheet 1.3 a C.t of 15 mg/L.min should achieve effective inactivation of enteric bacteria and viruses. With chlorinated/chloraminated supplies, it is common practice in Australia to endeavour to maintain adequate chlorine residual throughout the entire distribution system. Maintaining chlorine residual provides protection from backflow, ingress and Naegleria, and helps inhibit biofilm growth.

Where the aim is to maintain adequate disinfectant residual across the entire distribution system, the target chlorine residual set at the chlorinator will be based on achieving a desired residual concentration through most of the distribution system, including, where possible, the extremities of the system, after allowing for chlorine decay. As most chlorinators are designed to achieve a set residual to ensure a minimum C.t near the point of dosing the resultant C.t values will increase with longer contact time in the distribution system achieving a margin of safety.

The chlorine decay from the point of disinfection to the extremity of the distribution system is influenced by many factors including:

  • Water travel time/age

  • Chlorine demand of the water being disinfected

  • Water temperature

  • Biofilm growth

  • Asset condition of pipes and storages

All of these factors are dynamic. It is necessary to monitor the chlorine residual frequently within the distribution system, to enable adjustments of the chlorinator dosing rate to achieve the desired residual within the system.

If maintaining a consistent residual is difficult to achieve, or chlorine demand changes frequently, the water supplier should seek to understand the factors that are driving these changes. Some factors, such as water temperature, may be outside the water supplier’s control. However, other factors which may contribute to a sudden increase in chlorine demand (e.g. algal growth) may indicate an adverse event in the source water.

Whilst the absence of sufficient disinfectant residual does not necessarily mean the water is unsafe to drink, if the desired chlorine residual is not being achieved then corrective action needs to be taken to ensure the target value is achieved.

Managing water supplies with no residual

When used as disinfectants, ozone and UV light do not produce residuals within the distribution system. As discussed in the previous section, after effective disinfection, enteric pathogens should not reappear within the distribution system, unless there is a failure in the integrity of the system. In systems which lack residual disinfection, there is an increased need to ensure the integrity of the system to compensate for the absence of a residual.

In the Australian context, distribution systems that are suited to operating with no residual are those which have high quality source water (e.g. groundwater from a confined aquifer), or are small distribution systems, with a low water age within the distribution system, and which do not have embedded post-treatment storage tanks.

The attractions of operating distribution systems with no residual disinfection are that costs associated with maintaining residual disinfection are avoided, there are no issues with disinfection by-products, and it addresses the concerns of some consumers in relation to the use of chlorine. The main issues with no residual are that if the integrity of system is breached, there is no effective barrier to microbial contamination, and there can be additional costs involved with the cleaning and disinfection of the distribution system.

References

Austrian Standards Institute (ÖNORM) (2001). ÖNORM M 5873-1: Plants for the disinfection of water using ultraviolet radiation: Requirements and testing. Part 1. Low pressure mercury lamp plants. Österreichisches Normungsinstitut, A-1021 Vienna, Austria.

Austrian Standards Institute (ÖNORM) (2003). ÖNORM M 5873-2 Plants for the disinfection of water using ultraviolet radiation: Requirements and testing. Part 2. Medium pressure mercury lamp plants. Österreichisches Normungsinstitut, A-1021 Vienna, Austria.

Church J. and Colton J. (2013). Optimise chlorine contact Tank performance, WaterWorks, May 2013, 10-13, Water Industry Operators Association of Australia (WIOA), Shepparton, Australia.

Cutler D. and Miller G. (2005). The role of public health improvements in health advances: the twentieth-century United States. Demography 42:1-22.

German Association for Gas and Water (DVGW) (2006a). UV Devices for Disinfection in the Water Supply Part 1: Requirements Related to Composition, Function and Operation, in Technical Rule, Code of Practice W294-1. Deutsche Vereinigung des Gas- und Wasserfaches, Bonn, Germany.

German Association for Gas and Water (DVGW) (2006b). UV Devices for Disinfection in the Water Supply Part 2: Testing of Composition, Function and Disinfection Efficiency in Technical Rule, Code of Practice W294-2 Deutsche Vereinigung des Gas- und Wasserfaches, Bonn, Germany.

German Association for Gas and Water (DVGW) (2006c). UV Devices for Disinfection in the Water Supply; Part 3: Measuring Windows and Sensors for the Radiometric Monitoring of UV Disinfection Devices: Requirements, Testing and Calibration in Technical Rule, Code of Practice W 294-3 Deutsche Vereinigung des Gas- und Wasserfaches, Bonn, Germany.

National Water Research Institute (NWRI) (2012). Ultraviolet Disinfection Guidelines for Drinking Water and Water Reuse, Third Edition, California, United States of America.

US Centres for Disease Control and Prevention (1999). Morbidity and Mortality Weekly Report. Achievements in Public Health 1900-1999, Control of Infectious Diseases 48 (29) 621-629.

United States Environmental Protection Agency (US EPA) (2003). Guidance Manual for Disinfection Profiling and Benchmarking US EPA Office of Water: Washington D.C.

United States Environmental Protection Agency (US EPA) (2006). Ultraviolet disinfection guidance manual for the final long term 2 enhanced surface water treatment rule. US EPA Office of Water: Washington D.C.

World Health Organization (WHO) (2011). Guidelines for Drinking-water Quality, fourth edition, Geneva, Switzerland.

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