n-Octadecylphosphonic acid grafted mesoporous magnetic nanoparticle: Preparation, characterization, and application in magnetic solid-phase extraction

被引:132
作者
Ding, Jun [1 ]
Gao, Qiang [1 ,2 ]
Luo, Dan [1 ,3 ]
Shi, Zhi-Guo [1 ]
Feng, Yu-Qi [1 ]
机构
[1] Wuhan Univ, Dept Chem, Key Lab Analyt Chem Biol & Med, Minist Educ, Wuhan 430072, Peoples R China
[2] China Univ Geosci, Dept Fac Mat Sci & Chem Engn, Wuhan 430074, Peoples R China
[3] Shimadzu Int Trading Shanghai Co Ltd, Shimadzu Global COE Applicat & Tech Dev, Shanghai 200052, Peoples R China
关键词
n-Octadecylphosphonic acid; Magnetic nanoparticle; Magnetic solid-phase extraction; Polycyclic aromatic hydrocarbons; Lewis acid-base interaction; BAR SORPTIVE EXTRACTION; PERFORMANCE LIQUID-CHROMATOGRAPHY; POLYCYCLIC AROMATIC-HYDROCARBONS; ENVIRONMENTAL WATER SAMPLES; TOF-MS ANALYSIS; SELECTIVE ENRICHMENT; MASS SPECTROMETRY; HIGHLY EFFICIENT; STATIONARY-PHASE; FACILE SYNTHESIS;
D O I
10.1016/j.chroma.2010.09.074
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new sorbent for magnetic solid-phase extraction, n-octadecylphosphonic acid modified mesoporous magnetic nano particles (OPA/MMNPs), was easily prepared via a two-step strategy. MMNPs were synthesized by a solvent-thermal process, and then OPA was grafted onto the surface of MMNPs via the strong Lewis acid/base interaction. The resultant material was characterized by transmission electron microscopy, tensionmeter, Fourier-transform infrared spectroscopy, vibrating sample magnetometry, elemental analysis, and nitrogen adsorption analysis. The results demonstrated that the particles exhibited mesoporous structure, superparamagnetic (57 emu/g) and extremely hydrophobic (water contact angle of 136 degrees) properties. To evaluate the extraction performance of the resultant sorbent, polycyclic aromatic hydrocarbons (PAHs) were chosen as model analytes. The extraction conditions were optimized. Based on these, a rapid, convenient and efficient method for the determination of PAHs in water samples was established by combination of magnetic solid-phase extraction and gas chromatography-mass spectroscopy. The linearity range of proposed method was 0.2-100 mu g/L with correlation coefficients (R-2) of 0.9726-0.9970. The intra- and inter-day relative standard deviations (RSDs) were less than 17.6%. Batch-to-batch reproducibility was acceptable with RSD values less than 12.1%. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:7351 / 7358
页数:8
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