Discrete Element Method analysis reveals screen size impacts particle size distribution in pharmaceutical ribbons, suggesting optimized milling settings may enhance flow properties.
In the pharmaceutical industry, managing the flow properties of powder blends is challenging due to their poor flowability. Roller compaction mill, a key granulation technique, enhances the processability of these blends by compressing powders into dense ribbons, which are then milled into granules. This study employs Discrete Element Method (DEM) simulation to analyze the mechanical behavior and post-compaction dynamics of pharmaceutical ribbons, focusing on roll gap and screen size. The simulations reveal that the ribbon expands by up to 20% upon exiting the roller, with significant changes in volume fraction due to variations in roll gap. When the ribbon interacts with the mill impellers, it breaks upon contact, resulting in the formation of smaller clusters of particles as it passes through the screen. This study highlights the critical impact of screen size on particle size distribution (PSD), cluster count, and total volume. Moreover, the effect of roll gap on solid fraction of the ribbon and regional cluster distribution are studied thoroughly. Clearly, adjusting mill-screen design could optimize milling results, emphasizing the importance of controlling mechanical settings for better product uniformity and efficiency in solid dosage form manufacturing.
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De et al. (2025) studied this question.
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