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Ultrasonic characterization of aqueous solutions with varying sugar and ethanol content using multivariate regression methods

机译:使用多元回归方法对糖和乙醇含量不同的水溶液进行超声波表征

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This paper presents a multivariate regression method for simultaneous detection of sugar (sucrose as a sugar equivalent) and ethanol concentrations in aqueous solutions via temperature-dependent ultrasonic velocity. Thus, several samples of different combined concentration values were exposed to a temperature spectrum ranging from 2 to 30°C to investigate the temperature dependence of ultrasonic velocity. Model calibration was performed in order to predict the concentrations of interest. With results of proceeded experiments, the equations for calculation of unknown concentrations were carried out using polynomial regression revealing two equations with functional dependence of concentrations on each other. Further, side effects or systematic errors are still included in this model. To avoid such problems as well as to increase the accuracy with respect to the absolute errors in determining unknown probes, multivariate regression methods such as partial least squares (PLS) were tested and compared to the results obtained by polynomial regression. The accuracy achieved with chemometric models on average was three times higher. In direct comparison, the values of the error for the prediction of sucrose concentration were on average around 0.4 g/100 g in the regression model with polynomial background (RMPA) and around 0.12 g/100 g in the PLS model, and for ethanol concentration 0.13 and 0.04 g/100 g, respectively. Furthermore, calculations of the concentrations are possible without knowing the concentrations of the other solute.
机译:本文提出了一种多元回归方法,用于通过温度相关的超声速度同时检测水溶液中的糖(蔗糖的当量糖)和乙醇浓度。因此,将几个不同组合浓度值的样品暴露在2至30°C的温度范围内,以研究超声速度的温度依赖性。进行模型校准以预测目标浓度。根据进行中的实验结果,使用多项式回归进行了未知浓度的计算方程,揭示了两个浓度函数相互依赖的方程。此外,该模型中仍然包括副作用或系统错误。为了避免此类问题以及提高确定未知探针的绝对误差的准确性,测试了多元回归方法,例如偏最小二乘(PLS),并将其与多项式回归获得的结果进行了比较。化学计量模型所获得的准确度平均要高出三倍。直接比较,在多项式背景(RMPA)回归模型中,蔗糖浓度的预测误差值平均约为0.4 g / 100 g,在PLS模型中,乙醇浓度的误差平均值约为0.12 g / 100 g分别为0.13和0.04 g / 100 g。此外,可以在不知道其他溶质浓度的情况下计算浓度。

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