药物结晶过程的神经网络建模与模型控制研究

IF 3 Q2 ENGINEERING, CHEMICAL
P. Swapna Reddy , Amancha Sucharitha , Narendra Akiti , F. Fenila , Surendra Sasikumar Jampa
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引用次数: 0

摘要

溶剂的选择和操作参数的控制在间歇冷却结晶过程中起着至关重要的作用。为结晶过程选择最佳溶剂需要更多的实验和时间。为了克服这一问题,采用人工神经网络(ANN)模型技术,综合考虑不同溶剂的热力学性质,即临界温度、临界压力、温度、分子量和偏心因子,预测卡马西平形式Ⅲ溶解度。使用文献中可用的实验溶解度数据,对人工神经网络模型进行训练并评估其在各种输入数据集上的溶解度。有20个隐藏神经元的人工神经网络模型的R2值为0.9943,表明所建立的人工神经网络模型可用于间歇结晶过程中最佳溶剂的选择。此外,为了确定间歇冷却结晶过程的最佳冷却方式,利用“矩量法”技术,以最小变异系数(CV)和最大服从种群平衡方程的晶体平均尺寸(NMS)为目标,建立了多目标优化问题。提出了分段常数和分段线性两种温度策略,并采用NSGA-Ⅱ动态优化程序进行求解。通过分段线性策略获得的最优NMS值为197.1µm。该值比标称情况(未经优化)增加了28.3µm,变异系数从0.951降至0.76。此外,通过分段常数策略获得的最佳NMS值为205µm。该值增加了36.2µm,变异系数从0.951降低到0.73。这证明了通过多目标优化框架得到的最优冷却温度分布可以改善晶体属性。为了实现最优的冷却轮廓,一种先进的基于模型的控制,即通用模型控制(GMC)被开发出来。结果表明,GMC控制器具有良好的跟踪轮廓,无扰动偏移,以分段常数为设定点温度的均方根误差(RMSE)值较小,为0.0016。采用分段线性作为设定点温度,RMSE值为0.0018。尤其对于设定点轨迹跟踪问题,采用分段线性策略操作间歇冷却结晶过程是有利的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studies on crystallization process for pharmaceutical compounds using ANN modeling and model based control

Solvent selection and Controlling of operating parameters play a crucial role in batch cooling crystallization process. Choosing a best solvent for crystallization process involves more experimentation and time. To overcome this problem, an Artificial Neural Network (ANN) model technique is used to predict the carbamazepine form Ⅲ solubility by considering the thermodynamic properties of different solvents i.e. critical temperature, critical pressure, temperature, molecular weight, and acentric factor. The ANN model was trained and evaluated for solubility at various input data sets using experimental solubility data available in the literature. The ANN model with 20 hidden neurons has given the R2 value of 0.9943 which shows that the developed ANN model can be used for the selection of best solvent for batch crystallization process. Further, to determine the optimal cooling profile of batch cooling crystallization process, a multi-objective optimization problem is formulated by considering objectives as minimizing the coefficient of variation (CV) and maximizing the Number mean size (NMS) of crystals subjected to population balance equations using “method of moments” technique. Two types of temperature strategies i.e., piece-wise constant and piece-wise linear are developed and solved using NSGA-Ⅱ dynamic optimization procedure. The optimal NMS value attained through piece-wise linear strategy was 197.1 µm. This value has been increased by 28.3 µm from the nominal case (without optimization) and the coefficient of variation has decreased from 0.951 to 0.76. Further, optimal NMS value attained through piece-wise constant strategy was 205 µm. The value has been increased by 36.2 µm and the coefficient of variation has decreased from 0.951 to 0.73. This proves that the crystal attributes can be improved by optimal cooling temperature profile obtained by multi-objective optimization framework. For implementing the optimal cooling profile an advanced model-based control, i.e., Generic Model Control (GMC) was developed. It was observed that the GMC controller has the good tracking profile with no offset with/without disturbances and small value of root mean square error (RMSE) of 0.0016 using piece-wise constant as set point temperature. Using piece-wise linear as set point temperature, the RMSE value was 0.0018. In particular, it is advantageous to operate the batch cooling crystallization process with piece-wise linear strategy for set point trajectory tracking problems.

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