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DESIGN AND OPERATIONAL CONSIDERATIONS:

UV / AOP FOR INDIRECT POTABLE REUSE


1 2 2 3
Rory Morgan , Paul Swaim , Larry Schimmoller Cecile Bele
1. WaterSecure, Brisbane, QLD
2. CH2M Hill, Denver, USA
3. Veolia Water Services, Brisbane, QLD

ABSTRACT Other forms of Advanced Oxidation are available


and were considered, however none were proven
The recycling of wastewater into potable supplies on the scale of the project, within the economic
has received only limited application in the past, due constraints.
to both public perception issues and also
technological limitations. Recent advances, in UV/AOP
particular in supplementary processes such as
Advanced Oxidation have removed the impediment UV/AOP is, in simple terms, the incorporation of
of technological limitation, and allow water to be Ultraviolet disinfection into an Advanced Oxidation
created that is of significantly better quality that Process. By doing this, the UV/AOP provides three
most traditional drinking water supplies. highly effective methods of contaminant removal /
inactivation:
In Brisbane, South East Queensland, three water 1. Photolysis
recycling facilities have been constructed as part of 2. H2O2 oxidation
-
the Western Corridor Recycled Water Scheme. The 3. OH oxidation
Advanced Water Treatment Plants (AWTPs)
-
produce water equal to or better than Australian The OH radicals are formed when H2O2 is
Drinking Water Guidelines standard. To achieve subjected to ultraviolet light.
this water quality, a dual membrane approach is
utilised, with the RO permeate then passing through DESIGN OF UV / AOP
an Ultraviolet Radiation / Advanced Oxidation
(UV/AOP) Process. The design principles of the UV/AOP system were
developed on previous installations, as has been
This manuscript discusses the design and discussed in Swaim 2008, and modified for the
operational considerations associated with the particular demands of the project.
UV/AOP facility at the Luggage Point Advanced
Water Treatment Plant (AWTP). The production capacity of the Luggage Point
AWTP is 70ML/d and the UV/AOP units are
INTRODUCTION coupled to dedicated RO units, in a 3 Duty / 1
Standby arrangement. As such each UV/AOP unit
Previous papers (Morgan 2008) have detailed the is to treat 23.3ML/d. UV transmittance (UVT) is
circumstances in South East Queensland which monitored online, to allow dose control, while SBS
realised the Western Corridor Recycled Water (Sodium Bisulfite) is dosed downstream to quench
Project. Once the determination to allow for Indirect Hydrogen Peroxide (Figure 1).
Potable Reuse was made, the process flow
requirements were established. UV / AOP was Due to the requirement of the UV/AOP system to
included as a basic requirement for each plant due remove many compounds, two compounds are
to the following reasons: typically selected. These are:

1 – To provide an additional, verifiable barrier in 1 – NDMA


the multi-barrier process 2 – 1,4-Dioxane
2 – To remove microcontaminants, which in some
cases are not removed fully by RO, including: These indicator compounds are selected due to the
NDMA (Nitrosodimethylamine) and other difficulty of their removal, but also because they can
Nitrosamines; 1,4-Dioxane and other solvent be used to design the two principle components of
compounds; Pesticides and Herbicides; Taste and the UV/AOP system. NDMA is not impacted by
Odour causing compounds and algal toxins; H2O2 or OH-, so can be used to size the UV
Endocrine-Disrupting compounds (EDCs); component of the UV/AOP. Meanwhile 1,4-Dioxane
Pharmaceutical and personal care compounds; removal relied almost exclusively on oxidation by
-
Synthetic organic chemicals and Voltaile organics. H2O2 and OH , so can be used to size the
Hydrogen Peroxide (Advanced Oxidation) The scavenging tests involve simulation of the
component. reactors at bench scale to determine background
-
demand of OH . It was found that background
World’s best practice, principally developed by the demand was highly correlated to the concentration
California Health Department, was used in of chloramine in the water.
establishing the required removal for the 2 indicator
contaminants: Although similar reactors had been used and
validated on other projects, Computational Fluid
1 – NDMA removed to > 1.2 Log Removals Dynamics (CFD) analysis was carried out on the
2 – 1,4-Dioxane removed to > 0.5 Log Removals reactor design to model the particular flow
conditions on the project. This was done to ensure
Additional conditions established were a minimum minimal short circuiting, and ensure all flow that
contnuous dose of 500mJ/cm2 and a continuous passed through the reactor received equivalent
online validation of 4 log virus removal. dose (Figure 3).

A concentration limit of 10 ppt was also set for H2O2 QUENCHING


NDMA.
The UV / AOP utilises only 15% of the applied
FEEDWATER H2O2 dose, leaving approx 85% remaining in the
product water. This H2O2 must then be quenched.
The UV/AOP system was designed to treat the RO
permeate, and as such the following design Various quenching mechanisms are possible, but
parameters were included: the two commonly employed are quenching with
Sodium Hypochlorite or Sodium Bisulfite.
- UVT > 95%
- Monochloramine 1-2mg/L (as Cl2) Quenching with Sodium Hypochlorite requires a
considerable quantity of Sodium Hypochlorite. It
The RO permeate provided the benefit that was determined in bench scale testing that
automated cleaning mechanisms were not required. approximately 18mg/L NaOCl was required (based
on 5mg/L H2O2 residual).
UV REACTOR DESIGN
This was determined not to be feasible on account
Trojan UVPhox units were utilised in triple-deck of storage requirements, and also potential
arrangement. The units utilised Low Pressure, High generation of Chlorate, which was expected to
Output (LPHO) lamps operating at 254nm (Figure become and regulated water quality parameter
2). (although was not at the time).

Each train therefore comprised six (6) 72 lamp The design therefore allowed for quenching of
reactors representing a 5 Duty / 1 Standby H2O2 with Sodium Bisulfite. During initial operation
arrangement, for the design flow and this quenching was not successful, as the reaction
concentrations. Additionally each reactor of 72 between H2O2 and SBS did not proceed quickly
lamps allows for up to 6 lamps to fail before going enough, and realised an extremely high Sodium
offline. Hypochlorite demand (the plant requires a Free
Chlorine residual of 2mg/L). It was determined that
Lamp aging is considered in the design with the the addition of lime and consequent increase in pH
design power input based on the end of lamp life was slowing the reaction. Modifications were made
power draw of the lamps, which was guaranteed to to dose the SBS further upstream, allowing some
exceed 12,000 hours. reaction time before lime addition. Quenching was
then able to be carried out with approx 12-15mg/L
The EEO (a measure of the amount of energy SBS.
required per log removal of the target contaminant –
in this case NDMA) selected was based on VALIDATION
previously validated results from the same units at
other facilities. The EEO is used to determined the In establishing the multi-barrier process for these
required number of lamps and required energy AWTPs, it was determined that each barrier must
input. have Critical Control Parameters, that were to be
subject to validation, to ensure the integrity of the
The Hydrogen Peroxide dose was selected based barrier. For the UV/AOP, the parameter used are
on scavenging tests carried out on the feedwater, the Present Power Ratio (PPR) and the Hydrogen
and compared with rates used on similar projects. Peroxide dose. The PPR is a ration of the applied
At the minimum UVT of 95%, a dose rate of 6mg/L power divided by the required power, and is
was required (Figure 4). monitored continuously – it must always be greater
than 100%. The Hydrogen Peroxide dose rate is
also monitored continuously via a dedicated FIGURES
flowmeter, and this must always be above the
design value (of 6mg/L). SBS dose

OTHER OPERATIONAL ISSUES

Other operational issues observed in running the H2O2 dose Flow Monitoring
UV System
UV/AOP units were as follows:

- UVT meters required to be callibrated


regularly to ensure accurate measurement
Online UVT
- Monochloramine dose pre RO has a measurement Power Monitoring
significant impact on UVT (and hence required
power input)
Figure 1 : Process Flow Schematic UV/AOP
WATER QUALITY

All samples taken over the operational period have


shown NDMA and 1,4-Dioxane at below the limit of
detection. All other Australian Drinking Water
Guideline parameters have been met.

CONCLUSION

The UV / AOP system design for the Luggage Point


AWTP is into it’s second year of operations and has
proven to be reliable, and verifiable. It has assisted
in ensuring product water quality at all times
exceeds the stringent drinking water standards
applied.

ACKNOWLEDGEMENTS Figure 2 : Trojan UVPhox System

The authors would like to thank the following:

WaterSecure - Owner of the Western Corridor


facilities
Veolia - Operator of the Luggage Point AWTP

REFERENCES

Morgan, R, Solley, D, Thew, R, Edge, D,


Schimmoller, L, 2008. Advanced Nutrient Removal
for Indirect Potable Reuse, Ozwater 2008.

Swaim, P, Morgan, R, Foster, L, Mueller, P,


Vorissis, M, Erdal, U, Carter, W 2008. Implementing Figure 3 : CFD Analysis Extract
and Effective UV Advanced Oxidation Process,
ACE Water Reuse Conference
Required H2O2 Dose

6
Dose Rate (mg/L)

0
94% 95% 96% 97% 98% 99% 100%
UVT (% )

Figure 4 : Scavenging Test Results showing


required H2O2 dose

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