2012
DOI: 10.1016/j.scitotenv.2012.03.014
|View full text |Cite
|
Sign up to set email alerts
|

Separation of polybrominated diphenyl ethers in fish for compound-specific stable carbon isotope analysis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
14
0

Year Published

2013
2013
2020
2020

Publication Types

Select...
5

Relationship

3
2

Authors

Journals

citations
Cited by 7 publications
(15 citation statements)
references
References 27 publications
1
14
0
Order By: Relevance
“…The robustness of the method applied in the present study for PBDE CSIA has been verified in a previous study (Zeng et al, 2012b). GCeCeIRMS ion chromatograms (m/z ¼ 44) of the three fish extracts are shown in Fig.…”
Section: Precise and Accurate Compound Specific Carbon Isotope Analyssupporting
confidence: 76%
“…The robustness of the method applied in the present study for PBDE CSIA has been verified in a previous study (Zeng et al, 2012b). GCeCeIRMS ion chromatograms (m/z ¼ 44) of the three fish extracts are shown in Fig.…”
Section: Precise and Accurate Compound Specific Carbon Isotope Analyssupporting
confidence: 76%
“…Therefore, extensive purification steps are required to attain high-purity extracts before CSIA. The method for purification of PCBs in fish for compound-specific isotope analysis was based on our previous studies (Zeng et al, 2012(Zeng et al, , 2013a, with minor modifications. Briefly, the remainder of the fish carcass samples used for stable carbon isotope analysis was Soxhelt-extracted with 350 mL Hex/Acetone (1:1 v/v) for 72 h. The extract was concentrated to approximately 1 mL by rotary evaporator and the solvent exchanged with hexane (10 mL).…”
Section: Sample Preparation and Extractionmentioning
confidence: 99%
“…Degradation, especially biodegradation, is frequently accompanied by a substantial kinetic isotope effectd the heavier isotopes (here 13 C) react more slowly than the light isotopes in most chemical and biological reactions, and thus results in the enrichment of heavier isotopes in the remaining compounds and their depletion in the degradation products (Luo et al, 2013;Schmidt et al, 2004). The fractionation of stable isotopes (e.g., carbon, hydrogen, and nitrogen) generated by abiotic and biotic transformation of a compound is often significantly larger than that induced by phase-transfer processes, providing a unique approach for the identification and quantification of the transformation, and sometimes even for elucidating its mechanism (Schmidt et al, 2004;Zeng et al, 2012). The main benefit of using CSIA is the ability to track the fate of contaminants in complex matrices without the need to identify and quantify intermediates and metabolic products.…”
Section: Introductionmentioning
confidence: 99%
“…Determining the carbon isotope composition for a target organic pollutant requires sophisticated separation and purification procedures since background organic carbon and organic compounds with similar structures overshadow the carbon isotope signature of the target organic pollutant. The traditional CSIA method uses gas chromatography–combustion isotope ratio mass spectrometry (GC/C‐IRMS) and has been successfully applied in characterizing bioaccumulation processes and abiotic and biotic degradation of a wide range of persistent organic pollutants in the environment . Such a GC/C‐IRMS method was also used by Mai and colleagues for the measurement of the carbon isotope compositions of tri‐ to hexa‐BDEs in sediments and biological samples .…”
Section: Introductionmentioning
confidence: 99%
“…The traditional CSIA method uses gas chromatography–combustion isotope ratio mass spectrometry (GC/C‐IRMS) and has been successfully applied in characterizing bioaccumulation processes and abiotic and biotic degradation of a wide range of persistent organic pollutants in the environment . Such a GC/C‐IRMS method was also used by Mai and colleagues for the measurement of the carbon isotope compositions of tri‐ to hexa‐BDEs in sediments and biological samples . However, GC/C‐IRMS is not suitable for highly brominated PBDEs, especially for BDE‐209, because BDE‐209 is not thermally stable and tends to be incompletely combusted due to the inhibitory effect of Br − .…”
Section: Introductionmentioning
confidence: 99%