Pregled bibliografske jedinice broj: 1229508
Development and validation of HPLC method for the determination of n-nitrosamines in water
Development and validation of HPLC method for the determination of n-nitrosamines in water // IMEKO TC11 & TC24 Joint Hybrid Conference
Cavtat, Hrvatska, 2022. (predavanje, međunarodna recenzija, neobjavljeni rad, znanstveni)
CROSBI ID: 1229508 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Development and validation of HPLC method for the
determination of n-nitrosamines in water
Autori
Babić, Sandra ; Golub, Valentino ; Morović, Silvia ; Košutić, Krešimir
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, neobjavljeni rad, znanstveni
Skup
IMEKO TC11 & TC24 Joint Hybrid Conference
Mjesto i datum
Cavtat, Hrvatska, 17-19.10.2022
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
HPLC, N-nitrosamines, water, validation
Sažetak
The presence of N-nitrosamines in water is considered an emerging issue because they are highly carcinogenic and mutagenic to humans at trace levels. They can enter drinking water supplies mainly as a result of disinfection processes by the reaction between disinfectant (chloramine, chlorine and ozone) and the nitrogen- containing organic matter. Furthermore, nitrosamines are formed during some industrial processes such as cosmetics and food processing, leather tanning, rubber, pesticides and dyes manufacturing which can lead to their appearance in wastewater effluents. This work reports the development and validation of an analytical method for the quantitative determination of five N-nitrosamines namely N- nitrosomorpholine (NMOR), N-nitrosopirrolidine (NPYR), N-nitrosodiethylamine (NDEA), N- nitrosodipropylamine (NDPA), and N- nitrosodibutylamine (NDBA). The method is based on high performance liquid chromatography (HPLC) coupled to photo diode array (PDA) detector using Kinetex C18 column (150 mm × 4.6 mm, particle size 5 m, Phenomenex). Chromatographic separation was optimized regarding mobile phase composition and elution mode (isocratic and gradient). Prior to HPLC analysis, the off-line SPE preconcentration step was optimized to achieve low quantification limits. A coconut charcoal sorbent provided the best results in the preconcentration of 500 mL water samples. The optimized SPE-HPLC-PDA method was validated using tap water samples. A satisfactory linearity was obtained with R2 > 0.999 and limit of quantification at ngL-1 level. Validated method has been applied for the determination of N-nitrosamines removal efficiencies by reverse osmosis (RO) membrane treatment.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb