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Optimization-Based Process Synthesis for Integrated Crystallizer-Wet Mill System for Improved Crystal Shape Control

机译:用于改进晶体形状控制的集成结晶器湿磨机系统的优化工艺合成

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The simultaneous control of crystal size and shape is particularly important in fine chemical and pharmaceutical crystallization.These two quantities not only influence significantly the dissolution rate and bioavailability of final drug products,but also contribute to the manufacturability and efficiency of downstream operations.The manipulation of crystal shape,however,is difficult since it requires the decoupled growth rate control of individual crystal faces.The supersaturation and solvent system dependency of these rates are often not strong enough to enable impactful crystal shape control through temperature and/or solvent composition variation.The aim of this work is to analyse and evaluate the control possibilities of bivariate size distribution(which by definition involves crystal size and shape information)of high-aspect ratio crystals in an integrated crystallizer-external wet mill system.The crystallizer is modelled by primary and secondary nucleation,crystal growth and dissolution along the length and width axes,whereas in the wet mill-in addition to the aforementioned sub-processes-fragmentation and attrition are also considered.The advanced hydrodynamic description enables the direct implication of stirrer revolution speed in the model.The generated system of hyperbolic partial differential and ordinary differential equations is solved by the fully discretized high-resolution finite volume method,involving graphical processing unit acceleration,which brings significant-generally two orders of magnitude-speed-up.The dynamic optimization of wet-mill rotation speed,crystallizer temperature and recirculation flowrate revealed that the target bivariate crystal size distribution can be achieved much better with the integrated system than manipulating only the temperature profile of the batch crystallizer.
机译:同时控制晶体尺寸和形状在精细化学和药物结晶中尤为重要。这两种量不仅影响最终药品的溶解速率和生物利用度,而且还有助于下游操作的可制造性和效率。操纵然而,晶体形状是困难的,因为它需要单个水晶面的去耦生长速率控制。这些速率的过饱和和溶剂系统依赖性通常不足以使抗冲击性晶体形状控制能够通过温度和/或溶剂组成变化来实现抗冲击性晶体形状。该这项工作的目的是分析和评价一体化结晶器外湿磨系统中的高纵横比晶体的双抗体尺寸分布(其定义涉及晶体尺寸和形状信息)的控制可能性。结晶器由初级和次生成核,晶体生长和DIS沿长度和宽度轴的溶液,而在湿式磨机中 - 除了上述子过程 - 也考虑了碎片和磨损。先进的流体动力学描述能够直接暗示模型中的搅拌器旋转速度。产生的系统通过完全离散化的高分辨率有限体积法解决了双曲线部分差分和常规方程,涉及图形处理单元加速度,这使得显着的两个峰值速度。湿磨旋转速度的动态优化,结晶器温度和再循环流量揭示了靶肌晶体尺寸分布可以通过集成系统更好地实现,而不是仅操纵批料结晶器的温度曲线。

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