ppcps at a point source (publicly owned treatment works) … · 2015-01-21 · ppcps at a point...
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PPCPs at a Point Source (Publicly Owned Treatment Works) Discharge Before and After
Tertiary Disinfection by Chlorination
Jenny Pape,a Million Woudneh,b Richard Grace,b John Cosgrove,b
Greg Cavallo,c Ron MacGillivray,c Thomas Fikslinc
SETAC Portland
November 8th, 2010 a University of Victoriab AXYS Analytical Services
c Delaware River Basin Commission
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• PPCPs are being discovered and quantified in many water systems (surface, ground and to a lesser extent drinking water).
• PPCP methods are primarily focused on native analytes rather than transformation products.
• These analytes of emerging concern are termed “pseudo-persistent”.
• Current PPCP data may be misleading due to analyte speciation.
Background
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Does chlorination produce transformation products during wastewater treatment?
1. Field Reconnaissance – Extended EPA Method 1694 for occurrence in POTW effluent (3x for analyte consistency). Targets known to react with chlorine have been selected.
2. Bench Chlorination – a study of the chlorination of the selected analytes in reagent water to evaluate reactivity and the formation of transformation products was completed.
3. Matrix Chlorination – transformation products were demonstrated to form in a complex wastewater matrix.
4. Method Development – analytical quantification of parent compounds and transformation products was developed. Wastewater samples were analyzed before and after chlorine treatment.
Project Objective & Approach
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NonylphenolC15H24O
Triclosan
1. http://mapmaker.rutgers.edu/page1links.html.
Site Selection & Design
C12H7O2Cl3Triclosan
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Selected PPCPs Detected in Wastewater:
(ng/L) (ng/L)
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Wastewater Sampling
Triplicate wastewater samples obtained (June 25th, 28th, 29th)
Solids
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When free chlorine is providedtriclosan reacts rapidly consumingthe available chlorine.
0.7 mg/L, 1 equivalent Cl2
No free Cl2
2 min
Triclosan (2.5 μg/mL) is stable in a reagent water matrix over the experimental window when no chlorine is present.
Triclosan
Triclosan
TetraclosanPentaclosan
Instrumentalchloride adduct
Bench Study – Reagent Water
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2 hours
2 min
No free Cl2
10 mg/L, 19 equivalents Cl2
Reagent Water – Increased Chlorination
10 mg/L, 19 equivalents Cl2
TriclosanTriclosan
PentaclosanTrichlorophenol
Trichlorophenol
Pentaclosan
Pentaclosan
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Bench Study – Wastewater
Triclosan spiked into wastewater and chlorinated. No reaction is observed to occur, triclosan dominates the spectrum.
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Wastewater Breakpoint
Total Chlorine = Free Chlorine + Combined Chlorine
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Wastewater – Increased Chlorination
m/z 321
m/z 355
Tetraclosan
Pentaclosan
Transformation products are observedin wastewater at increased chlorination(~4.5x that of non-reacted wastewater).
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Quantitative Method Development
Target List
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Method Validation
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Wastewater Sampling
The selected publicly owned treatment works located near the Delaware River handles ~100 million gallons of sewage daily.
Samples were obtained on three separate days at both pre and post chlorination steps.
Sample chlorination was quenched prior to shipping using ascorbic acid. Samples were stored frozen in amber glass bottles upon receipt.
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Wastewater Results
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Field Sample Results
• Pre and post chlorination wastewater samples were found to contain both nonylphenol (ppb) and triclosan (ppt).
• Statistical analysis at a confidence level of 95% indicates that the means of the nonylphenol and triclosan concentrations are not significantly different after treatment.
• Specific transformation products were not observed above the reporting limit.
• These results are consistent with the wastewater benchtop study which required increased amounts of sodium hypochlorite to observe transformation products.
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Conclusions
Transformation products of triclosan and nonylphenol are not detected as a product of chlorine treatment in the studied publicly
owned treatment works.
In situations where free chlorine is available, transformation products would be expected and could potentially comprise the entire analyte
load, in particular for phenols.
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Next Steps...
• Analysis of wastewater samples from a treatment plant employing nitrification processes (more likely to have free chlorine present).
• Expansion of the target list to include other relevant targets and transformation products, in particular those which are phenolic in nature.
• Use of the developed method in conjunction with dioxin analysis(EPA Method 1613B) to obtainfurther information about theoccurrence and fate of triclosantransformation products.
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Acknowledgements:
Scott McIndoe
Million WoudnehGeorgina BrooksRichard GraceJohn Cosgrove
Greg CavalloRon MacGillivrayThomas Fikslin