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首页> 外文期刊>Journal of Colloid and Interface Science >Nano-sized molecularly imprinted polymer for selective ultrasound assisted microextraction of pesticide Carbaryl from water samples: Spectrophotometric determination
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Nano-sized molecularly imprinted polymer for selective ultrasound assisted microextraction of pesticide Carbaryl from water samples: Spectrophotometric determination

机译:用于选择性超声辅助水样中的纳米分子印迹聚合物从水样中的农药碳酸微萃取:分光光度法测定

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Ultrasound-assisted dispersive solid phase microextraction followed by UV-Vis spectrophotometry (UA-DSPME UV-Vis) was designed for the extraction and preconcentration of Carbaryl using nano-sized molecularly-imprinted polymer (MIP-NP). Nano-sized Carbaryl-imprinted polymer was characterized by scanning electron microscopy. A preliminary Plackett-Burman design was applied for screening. Subsequently, central composite design under response surface methodology was used to investigate and model the Carbaryl adsorption as response as well as to optimize this response versus variables such as Carbaryl MIP-NP mass, sonication time, temperature, eluent volume, pH and vortex time. At optimum experimental conditions, UAMSPE-UV-Vis exhibited a linear range of 0.1-1.2 mg L-1. The enhancement and preconcentration factors were obtained to be 30.6 and 25.0, respectively, for the extraction of Carbaryl by MIP-NP. In addition, the values of 0.033 and 0.11 mg L-1 were obtained for limit of detection and limit of quantification, respectively. The value of 4.3% determined for relative standard deviation for the separation and preconcentration of Carbaryl after 5 repetitions shows the acceptable repeatability of the process. Finally, the developed method was successfully applied for the determination of Carbaryl in water samples. (C) 2017 Elsevier Inc. All rights reserved.
机译:超声辅助分散固相微萃取,随后通过UV-Vis分光光度法(UA-DSPME紫外 - 可见)使用纳米尺寸的分子印迹聚合物(MIP-NP)设计用于西维因的提取和富集。通过扫描电子显微镜表征纳米型碳酸印迹聚合物。初步Plackett-Burman设计被应用用于筛选。随后,使用响应表面方法下的中央复合设计来研究和模拟Carbaryl吸附作为响应,以及优化该响应与变量,例如Carbaryl MIP-NP质量,超声处理时间,温度,洗脱液体积,pH和涡旋时间。在最佳实验条件下,UAMSpe-UV-Vis显示出0.1-1.2mg L-1的线性范围。通过MIP-NP将增强和预浓度因子分别为30.6和25.0,用于提取Carbaryl。另外,获得0.033和0.11mg L-1的值,分别用于检测和定量限制。在5重复后,对于碳酸的分离和前浓度的相对标准偏差确定的值为4.3%显示了该方法可接受的可重复性。最后,成功地应用了开发方法以测定水样中的碳酸。 (c)2017年Elsevier Inc.保留所有权利。

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