WATER PRODUCTION FOR AWARE (Organic Contaminants)
Antonio Cobelo
water sampling
water processing
water analysis
waste water treatment
advanced tertiary treatment SOP
Abstract
The protocol summarises the procedures used for analytical control. The protocol describes the Standard Operating Procedure (SOP) for the optimization of advanced tertiary treatment of water, based on a comprehensive quality and risk assessment.
Steps
Organic Contaminants:
The water production for AWARE main activities includes three stages – disinfection by ultraviolet C radiation (UVC), storage for12h 0m 0s
-24h 0m 0s
(according to water load and season) and ozonation. The water quality is monitored at these three stages, for the parameters indicated in Figure 1 below.

Sampling, Processing, and Analyses
Water samples are collected (see Figure 2) and processed within a6h 0m 0s
interval, before being shipped for the partner responsible for the analyses (Table 1). In case no processing is needed, samples are frozen and stored at-80°C
within3h 0m 0s
.
For each sampling event, the date, day of the week and hour; the temperature and rain. Sampling points, indicated in Figure 2 were designated from A to I:
-
Influent of primary treatment (A)
-
Influent of biological treatment (activated sludge) (B)
-
Treated secondary effluent (C)
-
Sand filter effluent (D)
-
UVC effluent (E)
-
Storage for reuse tank effluent (F)
-
Ozonation effluent (1 dose, e.g.,
5mg
O3) - MITO3X technology - (G) -
Effluent of the vacuum UV oxidation (VUV) (H)
-
Effluent of reactive storage / Influent of the recirculation aquaculture system (RAS) (I) ù

Methods: The section below summarises the procedures used for analytical control – detailed protocols are annexed to this protocol.
Organic Contaminants: Organic Contaminants:
Analysis: s: Screening of Organic Contaminants in Water.
Methods: Solid-phase extraction
2.1 Sample filtration 0.45um um PVDF).
Collect200mL
of the filtered water sample (e.g. volumetric flask or beaker) and spike with 50µL
of an internal standard solution. Produce two200mL
replicates per sample. Mix well after the internal standard is added.
Cleaning/Conditioning of the cartridges (OASIS HLB200mg
)
3.1. Pa5mL
s of MeOH
3.2. 5mL
ass of ultrapure water
Pass the200mL
of sample
Rinse the volumetric flask or beaker that contained the sample with 2x10mL
of ultrapure water, which are then passed through the cartridege
Drying the cartridge resin (e.g. N2 flow for0h 30m 0s
)
Store the cartridges in a freezer (-20°C
)
All samples are to be processed in duplicate.
For the cartridge blanks (n=2): star with , and then spike directly on the cartridge the same amount of internal standard as for sam50µL
les ( mL
ix de ). Then go direcly to .
For the ultrapure water blanks (n=2), the same type of sampling flasks are filled with ultrapur24h 0m 0s
water before sampling. Then they are treated using the same protocols as for samples.
Elution of the loaded cartridges was carried out by gra10mL
ity using of methanol f10mL
llowed by of dichloromethane. The eluates were concentrated approximat0.5mL
ly to ca. using a Turbovap II concentrator (Zymark, Hopkinton, MA, USA), then to dryness under a gentle nitrogen stream and finally recons500µL
ituted in of methanol and filte1ugmL
ed w13 mm
th a GHP‱ syringe filter (Pall Corporation). The extracts were injected in an Agilent 1290 LC coupled with and Agilent 550 QTOF system.
Parameters framed by Legal and Regulatory Requirements:
Using the EU Drinking Water Directive:
Organic contaminants - DIRECTIVE 2008/105/EC OF THE EUROPEAN PARLIAMENT AND THE
COUNCIL of 16 December 2008 on environmental quality standards in the field of water policy.