Evaluation of a cooling/heating-assisted microextraction instrument using a needle trap device packed with aminosilica/graphene oxide nanocomposites, covalently attached to cotton
文献情報
A. R. Ghiasvand, N. Heidari, S. Abdolhosseini, A. Hamdi, P. R. Haddad
A low-cost and reliable cooling/heating-assisted microextraction (CHaME) instrument was designed and fabricated for use in different modes of microextraction methods. The CHaME setup is able to cool down the sorbent and simultaneously heat the sample in a wide temperature range. Consequently, it can create a large thermal gap between the sorbent and the sample matrix, to promote the release of analytes from the sample tissue and enhance their effective trapping on the microextraction phase. The primary versions of the instrument have previously been evaluated, coupled with different modes of solid- and liquid-phase microextraction strategies. Compared with conventional microextraction systems, it is able to extract volatile organic compounds from complicated solid matrices more effectively, rapidly and without any need for a sample preparation step. In this research, the final and compact version of the CHaME instrument was fabricated and employed in a cooling/heating-assisted needle trap device (CHaME-NTD) for microextraction of polycyclic aromatic hydrocarbons (PAHs) in contaminated soil samples, prior to GC-FID determination. An aminosilica/graphene oxide nanocomposite was synthesized, covalently attached to cotton (Am-Si/GO/Cot), packed inside a needle, and applied as an effective sorbent for trapping of the analytes. The influence of experimental parameters on the extraction efficiency of the TC-NTD-GC-FID strategy was evaluated and optimized. Under the optimal conditions, linear dynamic ranges (LDRs), limits of detection (LODs), and relative standard deviations (RSDs) for the PAHs were 0.001–2.0 μg g−1, 5–38 pg g−1, and 6.2–9.8% (n = 6), respectively. The CHaME-NTD-GC-FID procedure was compared with the traditional NTD-GC-FID method. Additionally, the Am-Si/GO/Cot nanocomposite sorbent was compared with the most frequently used commercial sorbents. The results demonstrated the remarkable performance of the CHaME-NTD procedure and the Am-Si/GO/Cot composite sorbent. The developed setup was also used for the extraction and determination of PAHs in contaminated soil samples, through the CHaME-NTD-GC-FID procedure.
関連文献
The manner and extent to which the hydration shell impacts interactions between hydrated species
Jinyang Jiang, Le Guo, Luping Tang, Yu Zhang
DOI: 10.1039/D1CP03368A
Thermo-osmotic pressure and resistance to mass transport in a vapor-gap membrane
Michael T. Rauter, Sondre K. Schnell, Bjørn Hafskjold, Signe Kjelstrup
DOI: 10.1039/D0CP06556K
Correction: De novo prediction of cross-effect efficiency for magic angle spinning dynamic nuclear polarization
Anne-Laure Barra, Johan van Tol, Sabine Hediger, Daniel Lee, Gaël De Paëpe
DOI: 10.1039/D1CP90117F
Computational discovery of PtS2/GaSe van der Waals heterostructure for solar energy applications
Rui Xiong, Rong Hu, Yinggan Zhang, Xuhui Yang, Peng Lin, Cuilian Wen, Baisheng Sa, Zhimei Sun
DOI: 10.1039/D1CP02436A
Atmospheric oxidation of fluoroalcohols initiated by ˙OH radicals in the presence of water and mineral dusts: mechanism, kinetics, and risk assessment
Feng-Yang Bai, Ming-Shuai Deng, Mei-Yan Chen, Lian Kong, Shuang Ni, Xiu-Mei Pan
DOI: 10.1039/D1CP01324F
Self-assembled, optically-active {naphthalene diimide}U{cucurbit[8]uril} ensembles in an aqueous environment
Heather F. Higginbotham, Subashani Maniam, Tina Hsia, Lyle Isaacs, Steven J. Langford, Toby D. M. Bell
DOI: 10.1039/D1CP00659B
An experimental and master-equation modeling study of the kinetics of the reaction between resonance-stabilized (CH3)2CCHCH2 radical and molecular oxygen
Satya P. Joshi, Timo T. Pekkanen, Prasenjit Seal, Raimo S. Timonen, Arkke J. Eskola
DOI: 10.1039/D1CP02210E
Impact of Cu(ii) and Al(iii) on the conformational landscape of amyloidβ1-42
Lorena Roldán-Martín, Francesca Peccati, Mariona Sodupe, Jean-Didier Maréchal
DOI: 10.1039/D1CP01561C
First-principles-based kinetic Monte Carlo simulations of CO oxidation on catalytic Au(110) and Ag(110) surfaces
Jose L. C. Fajín, Ana S. Moura, M. Natália D. S. Cordeiro
DOI: 10.1039/D1CP00729G
Resistive switching on individual V2O5 nanoparticles encapsulated in fluorinated graphene films
Artem I. Ivanov, Victor Ya. Prinz, Irina V. Antonova, Anton K. Gutakovskii
DOI: 10.1039/D1CP02930D
こちらもおすすめ
3-イチチルビフェニルはどのように合成されますか?
3-イチチルビフェニルは、ビフェニルとイチプロピオニトリルを回収率約90%で反応させて合成されます。触媒は通常、亜リチウムホウ素を用います。
8-溴-5-三氟甲基喹啉はどのように合成されますか?
8-溴-5-三氟甲基喹啉は、5-トリフルオロメチル-2-メチル-1,3-ベンゼンジオールをブロモエタノールと反応させて生成します。この反応は塩基性条件下で行われ...
ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品はありますか?
ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品としては、4-...
N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向や研究トレンドはどのようなものでしょうか?
N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向は、主に産業用途での需要により影響を受けます。研究トレンドとし...
イソステアロイルグリセリルは安全ですか?
イソステアロイルグリセリルは一般的に安全性が高いとされていますが、過度な使用や個人差により皮�owsん炎などの反応が起こる可能性があります。使用前に医師に相談す...
1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向や研究トレンドはどうですか?
1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向は、医薬品や合成化学の研究分野で注目を集めています。新興研究は、該当化合物の合成改良と生体内での作用メカニズ...
3-チオフェンスチオールの物理化学的性質は何ですか?
3-チオフェンスチオールのCAS番号は7774-73-4です。結晶性の白色粉末で、分子量は122.17です。この化合物は水に微溶解し、エタノールやジクロロメタン...
2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは安全ですか?
2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは一定の安全性基準を満たしていま...
CAS番号1316822-90-8の化合物は安全ですか?
CAS番号1316822-90-8の化合物は安全性に関しては評価が不足していますが、一般的には生物学的に活性な物質であり、取り扱いには適切な安全防護措置が必要で...
Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸はどのように保存すればよいですか?
Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸は、冷暗所で保存し、直射日光から遠ざけてください。容器は密閉し、高湿度や高温を避けて保管してください。
掲載誌
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.











![N-{15-[(2,5-Dioxo-1-pyrrolidinyl)oxy]-15-oxo-3,6,9,12-tetraoxapentadec-1-yl}-2-(2-propyn-1-yloxy)acetamide structure N-{15-[(2,5-Dioxo-1-pyrrolidinyl)oxy]-15-oxo-3,6,9,12-tetraoxapentadec-1-yl}-2-(2-propyn-1-yloxy)acetamide structure](https://static.chemtradehub.com/structs/210/2101206-92-0-2eb5.webp)
![(2R,6S)-6-[(Benzyloxy)methyl]-4-{[(2-methyl-2-propanyl)oxy]carbonyl}-2-morpholinecarboxylic acid structure (2R,6S)-6-[(Benzyloxy)methyl]-4-{[(2-methyl-2-propanyl)oxy]carbonyl}-2-morpholinecarboxylic acid structure](https://static.chemtradehub.com/structs/109/1093085-91-6-3382.webp)
