TY - JOUR
T1 - A hollow microporous organic network as a fiber coating for solid-phase microextraction of short-chain chlorinated hydrocarbons
AU - Li, Jingkun
AU - Li, Huijuan
AU - Zhao, Yanfang
AU - Wang, Shanshan
AU - Chen, Xiangfeng
AU - Zhao, Ru Song
N1 - Publisher Copyright:
© 2018, Springer-Verlag GmbH Austria, part of Springer Nature.
PY - 2018/9/1
Y1 - 2018/9/1
N2 - A solid-phase microextraction (SPME) fiber coated with a hollow microporous organic network (H-MON) was fabricated for the analysis of short-chain chlorinated paraffins (SCCPs). The sorbent was prepared by reacting tetra(4-ethynylphenyl)methane and 1,4-diiodobenzene using bis-(triphenylphosphine) palladium(II) as the catalyst in the presence of silica sphere templates, which then were removed by hydrofluoric acid. The SCCPs were quantified by GC-MS working in the negative chemical ionization mode. The H-MON has a high specific surface (701 m2·g−1) and microporosity (pore size <2 nm). Extraction temperature, extraction time, and ionic strength of the sample solutions were optimized by using the Box-Behnken design. The head-space SPME exhibits better extraction performance than the direct immersion mode. Under optimal working conditions, the detection limit (3 times of the standard deviation) is 0.03 ng·mL−1 in the water samples. Response is linear in the 0.05–10 ng·mL−1 concentration range. Repeatability and reproducibility, expressed as the relative standard deviations, ranged from 4.6 to 11.0%. The method was successfully applied in the analysis of SCCPs in water, sediments, organisms, and atmospheric particulate matter samples. [Figure not available: see fulltext.].
AB - A solid-phase microextraction (SPME) fiber coated with a hollow microporous organic network (H-MON) was fabricated for the analysis of short-chain chlorinated paraffins (SCCPs). The sorbent was prepared by reacting tetra(4-ethynylphenyl)methane and 1,4-diiodobenzene using bis-(triphenylphosphine) palladium(II) as the catalyst in the presence of silica sphere templates, which then were removed by hydrofluoric acid. The SCCPs were quantified by GC-MS working in the negative chemical ionization mode. The H-MON has a high specific surface (701 m2·g−1) and microporosity (pore size <2 nm). Extraction temperature, extraction time, and ionic strength of the sample solutions were optimized by using the Box-Behnken design. The head-space SPME exhibits better extraction performance than the direct immersion mode. Under optimal working conditions, the detection limit (3 times of the standard deviation) is 0.03 ng·mL−1 in the water samples. Response is linear in the 0.05–10 ng·mL−1 concentration range. Repeatability and reproducibility, expressed as the relative standard deviations, ranged from 4.6 to 11.0%. The method was successfully applied in the analysis of SCCPs in water, sediments, organisms, and atmospheric particulate matter samples. [Figure not available: see fulltext.].
KW - Atmospheric particulate matter
KW - Box-Behnken design
KW - Gas chromatography mass spectrometry
KW - Hollow microporous organic network
KW - Negative chemical ionization
KW - Organisms
KW - Sediments
KW - Short-chain chlorinated paraffins
KW - Solid-phase microextraction
KW - Water samples
UR - http://www.scopus.com/inward/record.url?scp=85051626649&partnerID=8YFLogxK
U2 - 10.1007/s00604-018-2955-7
DO - 10.1007/s00604-018-2955-7
M3 - Article
C2 - 30120575
AN - SCOPUS:85051626649
SN - 0026-3672
VL - 185
JO - Microchimica Acta
JF - Microchimica Acta
IS - 9
M1 - 416
ER -