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首页> 外文期刊>Iranian polymer journal >Chitosan-based magnetic molecularly imprinted polymer: synthesis and application in selective recognition of tricyclazole from rice and water samples
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Chitosan-based magnetic molecularly imprinted polymer: synthesis and application in selective recognition of tricyclazole from rice and water samples

机译:基于壳聚糖的磁性分子印迹聚合物:合成及应用在水稻和水样中三环唑的选择性识别

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摘要

A tricyclazole selective chitosan/Fe(3)O(4)magnetic molecularly imprinted polymer (MMIP) was synthesized using non-covalent binding polymerization involving methacrylic acid (MAA) as functional monomer, divinylbenzene (DVB-80) as crosslinker, 2,2'-azobisisobutyronitrile as initiator, acetonitrile/toluene (75:25, v/v) as porogenic solvent and tricyclazole as template. Surface morphology and magnetic characterization of the prepared imprinted and non-imprinted polymers were done using scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectrometry and vibrating sample magnetometry, respectively. The adsorption kinetic data fitted best in pseudo-second-order model. The adsorption equilibrium was achieved in 30 min and the maximum binding capacity was 4579.9 mu g/g. The Freundlich isotherm model was found suitable for explaining the binding isotherm data (R-2 0.99). Negative values of thermodynamic parameters increment G(Gibb's free energy), increment H(enthalpy), and increment S(entropy) revealed exothermic and spontaneous nature of adsorption processes. It also revealed decreased randomness at the solid-liquid interface during sorption. The scatchard plot analysis suggested heterogeneity of binding sites on MMIPs. The molecular recognition selectivity of MMIPs towards tricyclazole was much higher, as compared to its structural analogues, tebuconazole (alpha = 28.58) and hexaconazole (alpha = 37.16). The MMIPs were successfully applied to separate and enrich tricyclazole from fortified samples of rice and water, with a recovery percentage of 89.4% and 90.9%, respectively. These reusable imprinted polymers possessing high selectivity and specificity can be utilized as an adsorbent for solid-phase extraction in sample preparation for tricyclazole residue analysis in complex environmental matrices.
机译:使用涉及甲基丙烯酸(MAA)作为功能单体,二乙烯基苯(DVB-80)作为交联剂,合成三环唑选择性壳聚糖/ Fe(4)磁性分子印迹聚合物(MMIP)作为交联剂,二氯苯乙烯(DVB-80)作为交联剂,2,2 '---引发剂,乙腈/甲苯(75:25,v / v)作为致致溶剂和三环唑作为模板。使用扫描电子显微镜,透射电子显微镜,傅里叶变换红外光谱和振动样品磁体进行制备的印迹和非印记聚合物的表面形态和磁表征。吸附动力学数据在伪二阶模型中最适合。在30分钟内实现吸附平衡,最大结合能力为4579.9μg/ g。发现Freundlich等温模型适用于解释结合等温数据(R-2> 0.99)。热力学参数的负值增量g(Gibb的自由能),增量h(焓)和增量S(熵)揭示了吸附过程的放热和自发性。它还揭示了吸附过程中的固液界面随机性下降。 Scatchard绘图分析表明MMIPS上的结合位点的异质性。与其结构类似物,Tebuconazole(α= 28.58)和六丙二醇(α= 37.16)相比,MMIP的MMIPS朝向三环唑的分子识别选择性要高得多。 MMIP成功地应用于与水稻和水的强化样品分离并富含三环唑,分别恢复百分比89.4%和90.9%。这些可重复使用的印迹聚合物具有高选择性和特异性,可以用作复杂环境基质中三环唑残留分析的样品制剂中的固相提取的吸附剂。

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