TY - JOUR
T1 - Automated method using direct-immersion solid-phase microextraction and on-fiber derivatization coupled with comprehensive two-dimensional gas chromatography high-resolution mass spectrometry for profiling naphthenic acids in produced water
AU - Crucello, Juliana
AU - Sampaio, Naiara MFM
AU - Junior, Iris Medeiros
AU - Carvalho, Rogerio Mesquita
AU - Gionfriddo, Emanuela
AU - Marriott, Philip J.
AU - Hantao, Leandro Wang
N1 - Funding Information:
This study was financed by ANP/PETROBRAS (Grant 2019/00209-3 and 2019/00210-1 , Brazil), the National Council for Scientific and Technological Development (CNPq) (Grant 302748/2018-0 and 316202/2021-5 ), the São Paulo Research Foundation (FAPESP) (Grant 14/50867-3 and 20/01064-6 ), and the Coordination for the Improvement of Higher Education Personnel (CAPES) - Finance Code 001.
Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/3/15
Y1 - 2023/3/15
N2 - Naphthenic acids (NAs) are naturally occurring organic acids in petroleum and are found in waste waters generated during oil production (produced water, PW). Profiling this class of compounds is important due to flow assurance during oil exploration. Compositional analysis of PW is also relevant for waste treatment to reduce negative impacts on the environment. Here, comprehensive two-dimensional gas chromatography coupled with high-resolution mass spectrometry (GC×GC–HRMS) was applied as an ideal platform for qualitative analysis of NAs by combining the high peak capacity of the composite system with automated scripts for group-type identification based on accurate mass measurements and fragmentation patterns. To achieve high-throughput profiling of NAs in PW samples, direct-immersion solid phase microextraction (DI-SPME) was selected for extraction, derivatization and preconcentration. A fully automated DI-SPME method was developed to combine extraction, fiber rinsing and drying, and on-fiber derivatization with N-methyl-N‑tert-butyldimethylsilyltrifluoroacetamide (MTBSTFA). Data processing was based on filtering scripts using the Computer Language for Identifying Chemicals (CLIC). The method successfully identified up to 94 NAs comprising carbon numbers between 6 and 18 and hydrogen deficiency values ranging from 0 to -4. The proposed method demonstrated wider extraction coverage compared to traditional liquid-liquid extraction (LLE) – a critical factor for petroleomic investigations. The method developed also enabled quantitative analysis, exhibiting detection limits of 0.5 ng L−1 and relative standard deviation (RSD) at a concentration of NAs of 30 µg L−1 ranging from 4.5 to 25.0%.
AB - Naphthenic acids (NAs) are naturally occurring organic acids in petroleum and are found in waste waters generated during oil production (produced water, PW). Profiling this class of compounds is important due to flow assurance during oil exploration. Compositional analysis of PW is also relevant for waste treatment to reduce negative impacts on the environment. Here, comprehensive two-dimensional gas chromatography coupled with high-resolution mass spectrometry (GC×GC–HRMS) was applied as an ideal platform for qualitative analysis of NAs by combining the high peak capacity of the composite system with automated scripts for group-type identification based on accurate mass measurements and fragmentation patterns. To achieve high-throughput profiling of NAs in PW samples, direct-immersion solid phase microextraction (DI-SPME) was selected for extraction, derivatization and preconcentration. A fully automated DI-SPME method was developed to combine extraction, fiber rinsing and drying, and on-fiber derivatization with N-methyl-N‑tert-butyldimethylsilyltrifluoroacetamide (MTBSTFA). Data processing was based on filtering scripts using the Computer Language for Identifying Chemicals (CLIC). The method successfully identified up to 94 NAs comprising carbon numbers between 6 and 18 and hydrogen deficiency values ranging from 0 to -4. The proposed method demonstrated wider extraction coverage compared to traditional liquid-liquid extraction (LLE) – a critical factor for petroleomic investigations. The method developed also enabled quantitative analysis, exhibiting detection limits of 0.5 ng L−1 and relative standard deviation (RSD) at a concentration of NAs of 30 µg L−1 ranging from 4.5 to 25.0%.
KW - Environmental
KW - GCxGC
KW - Green chemistry
KW - Oil and gas
KW - Orbitrap
UR - http://www.scopus.com/inward/record.url?scp=85147605701&partnerID=8YFLogxK
U2 - 10.1016/j.chroma.2023.463844
DO - 10.1016/j.chroma.2023.463844
M3 - Article
AN - SCOPUS:85147605701
SN - 0021-9673
VL - 1692
JO - Journal of Chromatography A
JF - Journal of Chromatography A
M1 - 463844
ER -