摘要
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.].
| 源语言 | 英语 |
|---|---|
| 文章编号 | 416 |
| 期刊 | Microchimica Acta |
| 卷 | 185 |
| 期 | 9 |
| DOI | |
| 出版状态 | 已出版 - 1 9月 2018 |
| 已对外发布 | 是 |
指纹
探究 'A hollow microporous organic network as a fiber coating for solid-phase microextraction of short-chain chlorinated hydrocarbons' 的科研主题。它们共同构成独一无二的指纹。引用此
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver