首页> 美国卫生研究院文献>Sensors (Basel Switzerland) >Development of a Sequential Injection Analysis System for the Determination of Saccharin
【2h】

Development of a Sequential Injection Analysis System for the Determination of Saccharin

机译:顺序注射分析法测定糖精的系统开发

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Saccharin is a powerfully sweet nonnutritive sweetener that has been approved for food-processing applications within the range of 100–1200 mg/kg. A simple, rapid, and cost-effective sequential injection analysis (SIA) technique was developed to determine the saccharin level. This method is based on the reaction of saccharin with p-chloranil in an ethanol medium with a hydrogen peroxide (H2O2) acceleration, and the resultant violet-red compound was detected using a UV-Vis spectrophotometer at λmax = 420 nm. To ascertain the optimal conditions for the SIA system, several parameters were investigated, including buffer flow rate and volume, p-chloranil concentration, and reactant volumes (saccharin, p-chloranil, and H2O2). The optimum setup of the SIA system was achieved with a buffer flow rate, buffer volume, and draw-up time of 1.2 mL/min, 2900 µL, and ~145 s, respectively. The optimal p-chloranil concentration is 30 mM, and the best reactant volumes, presented in an ordered sequence, are as follows: 30 µL of H2O2, 450 µL of saccharin, and 150 µL of p-chloranil. The optimized SIA configuration produced a good linear calibration curve with a correlation coefficient (R2 = 0.9812) in the concentration range of 20–140 mg/L and with a detection limit of 19.69 mg/L. Analytical applications in different food categories also showed acceptable recovery values in the range of 93.1–111.5%. This simple and rapid SIA system offers great feasibility for the saccharin quality control in food-product processing.
机译:糖精是一种强力的甜味非营养性甜味剂,已被批准用于食品加工应用,范围为100-1200 mg / kg。开发了一种简单,快速且经济高效的顺序注射分析(SIA)技术来确定糖精水平。该方法基于糖精与对氯苯甲醛在乙醇介质中以过氧化氢(H2O2)促进的反应,使用紫外可见分光光度计在λmax= 420 nm下检测所得的紫红色化合物。为了确定SIA系统的最佳条件,研究了几个参数,包括缓冲液流速和体积,对氯苯醌浓度和反应物体积(糖精,对氯苯醌和H2O2)。通过缓冲液流速,缓冲液体积和吸取时间分别为1.2 mL / min,2900 µL和〜145 s,可以实现SIA系统的最佳设置。最佳对氯腈浓度为30 mM,按顺序显示的最佳反应物体积如下:30 µL H2O2、450 µL糖精和150 µL对氯腈。优化的SIA配置产生了良好的线性校准曲线,其相关系数(R 2 = 0.9812)在20–140 mg / L的浓度范围内,检出限为19.69 mg / L。在不同食品类别中的分析应用也显示出可接受的回收值,范围为93.1–111.5%。这种简单,快速的SIA系统为食品加工中的糖精质量控制提供了巨大的可行性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号