Microporous organic networks (MONs) are a potential class of microporous materials in analytical chemistry. As great efforts have been made in sample pretreatment and gas chromatography, the application of MONs in high performance liquid chromatography (HPLC) has largely lagged and has never been investigated. In addition, directly packing of MONs into columns for HPLC is impractical due to the high column pressure and low column efficiency resulted from the sub-micron sized and irregular MONs. To solve these issues and uncover the possibility of MONs in HPLC, here we report the fabrication of spherical silica amino-functionalized MON (SiO@MON-NH) composite as a novel stationary phase for HPLC. Neutral, acidic and alkaline probes were evaluated on SiO@MON-NH packed column. A column efficiency of 21,246 plates per meter was obtained for n-propylbenzene. The results revealed the hydrophobic interaction was the main separation mechanism on SiO@MON-NH packed column. Baseline separation of benzenediol, dichlorophenol, chlorophenol and phenylenediamine position isomers, deoxynucleosides and nucleosides was also achieved on SiO@MON-NH packed column. The relative standard deviations of retention time, peak height and peak area for the studied position isomers, deoxynucleosides and nucleosides were 0.2-0.7%, 0.3-3.7% and 1.7-3.5%, respectively. The SiO@MON-NH packed column also offered better resolution for dichlorophenol isomers, deoxynucleosides and nucleosides than SiO-NH and commercial C18 columns. These results revealed the potential of MONs in HPLC and also provided a new way for the use of nano-sized or irregular MONs in HPLC.
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http://dx.doi.org/10.1016/j.talanta.2020.121570 | DOI Listing |
Anal Methods
November 2017
College of Environmental and Chemical Engineering, Nanchang Hangkong University, Nanchang 330063, China.
A novel method was established using a restricted access material combined with a molecularly imprinted polymer (RAM-MIP) as the sorbent material in solid phase extraction (SPE) for clean-up of α-endosulfan, β-endosulfan, endosulfate, endosulfan-ether, endosulfan lactone, heptachlor, heptachlor--epoxide, and heptachlor--epoxide in pork and gas chromatography (GC) for determination. The RAM-MIP was prepared by precipitation polymerization by using endosulfan as the template, methacrylic acid (MAA) as the monomer, glycidyl methacrylate (GMA) as the pro-hydrophilic co-monomer, ethylene glycol dimethacrylate (EGDMA) as the crosslinker, azobisisobutyronitrile (AIBN) as the initiator, and toluene as the porogen. Ultraviolet spectroscopy (UV) and H-nuclear magnetic resonance (H-NMR) analysis verified that MAA interacted specifically with endosulfan in a ratio of 1 : 1 in the pre-polymerization solution.
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Zhejiang Engineering Research Center for Tissue Repair Materials and Wenzhou Key Laboratory of Biomaterials and Engineering and Wenzhou Key Laboratory of Biophysics, Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou 325001, China.
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