School of Pharmacy, Southwest Medical University, Luzhou, Sichuan, 646000, China.
School of Pharmaceutical Sciences, Chongqing University, Chongqing, 401331, China.
J Chromatogr A. 2020 Oct 11;1629:461476. doi: 10.1016/j.chroma.2020.461476. Epub 2020 Aug 15.
Core-shell structured magnetic covalent organic frameworks (FeO@COFs) were synthesized via a facile approach at room temperature using 1,3,5-tris(4-aminophenyl)benzene (TAPB) and 2,5-dibromo-1,4-benzenedicarboxaldehyde (DBDA) as two building blocks for the first time. The FeO@COFs were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier-transform infrared (FT-IR) spectroscopy, powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), nitrogen adsorption-desorption isotherms, and zeta potentiometric analysis. The FeO@COFs had a high specific surface area (141.94 m·g) and uniform pore size distribution (average 4.53 nm). They also demonstrated good magnetic response (32.49 emu·g) and good thermal and chemical stabilities. Furthermore, adsorption experiments were conducted to evaluate the adsorption capacities and adsorption times of FeO@COFs to diphenylamine (DPA) and its analogs, including benzidine (BZ), 1-naphthylamine (1-NA), 4-phenylphenol (4-PP), and O-tolidine (O-TD). From the experimental results, the maximum adsorption capacities of DPA, 1-NA, 4-PP, BZ, and O-TD were calculated as 246.25, 95.20, 85.85, 107.20, and 123.55 mg·g, respectively. A duration of 20 min was sufficient for adsorption. The FeO@COFs were explored as adsorbents for magnetic solid-phase extraction (MSPE) of DPA and its analogs, and the MSPE parameters, including adsorbent dosage, extraction time, pH, ionic strength, desorption solvent, desorption time, and desorption frequency were optimized. Combined with HPLC using diode-array detection, a simple, fast, and sensitive method was proposed to detect DPA and its analogs, which exhibited good linearity (r >0.9946) in the range of 0.1-100 μg·mL. Moreover, the low limits of detection (ranging from 0.02 to 0.08 μg·mL, S/N = 3), low limits of quantitation (ranging from 0.05 to 0.30 μg·mL, S/N = 10), good precision with low relative SDs (<5.86% for intra-day and <6.44% for inter-day) were obtained. Finally, FeO@COFs were applied to the effective MSPE of DPA and its analogs in actual samples chosen from the natural environment, and good recoveries (ranging from 79.97 to 122.52%) were observed.
核壳结构的磁性共价有机框架(FeO@COFs)是通过在室温下使用 1,3,5-三(4-氨基苯基)苯(TAPB)和 2,5-二溴-1,4-苯二甲醛(DBDA)作为两个构建块,首次通过简便的方法合成的。FeO@COFs 通过扫描电子显微镜(SEM)、透射电子显微镜(TEM)、傅里叶变换红外(FT-IR)光谱、粉末 X 射线衍射(XRD)、X 射线光电子能谱(XPS)、热重分析(TGA)、振动样品磁强计(VSM)、氮气吸附-解吸等温线和动电位滴定分析进行了表征。FeO@COFs 具有高比表面积(141.94 m·g)和均匀的孔径分布(平均 4.53 nm)。它们还表现出良好的磁响应(32.49 emu·g)和良好的热稳定性和化学稳定性。此外,还进行了吸附实验,以评估 FeO@COFs 对二苯胺(DPA)及其类似物,包括联苯胺(BZ)、1-萘胺(1-NA)、4-苯基苯酚(4-PP)和邻甲苯胺(O-TD)的吸附容量和吸附时间。从实验结果可知,DPA、1-NA、4-PP、BZ 和 O-TD 的最大吸附容量分别计算为 246.25、95.20、85.85、107.20 和 123.55 mg·g。吸附时间 20 min 即可满足吸附要求。FeO@COFs 被探索用作 DPA 和其类似物的磁固相萃取(MSPE)的吸附剂,并且优化了 MSPE 参数,包括吸附剂用量、萃取时间、pH 值、离子强度、洗脱溶剂、洗脱时间和洗脱频率。结合使用二极管阵列检测的高效液相色谱法,提出了一种简单、快速、灵敏的方法来检测 DPA 和其类似物,在 0.1-100 μg·mL 的范围内表现出良好的线性(r>0.9946)。此外,还获得了较低的检测限(范围为 0.02 至 0.08 μg·mL,S/N=3)、定量限(范围为 0.05 至 0.30 μg·mL,S/N=10)、日内相对标准偏差(<5.86%)和日间相对标准偏差(<6.44%)低的精密度。最后,将 FeO@COFs 应用于从自然环境中选择的实际样品中 DPA 和其类似物的有效 MSPE,观察到良好的回收率(范围为 79.97 至 122.52%)。