Powder Delumping System

Semi-Automated Pharmaceutical Powder Delumping System

Handling difficult-to-mix pharmaceutical and biopharmaceutical powders often results in stubborn blocks and agglomerations that can halt production. Our semi-automated powder delumping system is engineered specifically to solve this challenge. By rapidly deagglomerating compacted powders into a highly flowable state, this system keeps your processes moving efficiently, eliminates time-consuming manual delumping efforts, and ultimately protects the integrity of your finished product batches.

High-Efficiency Deagglomeration & Protection

Ensure seamless transitions from raw material storage to active mixing:

Precision Size Reduction: Delivers high deagglomeration efficiency by rapidly reducing hard powder blocks to uniform particles smaller than 10 mm.
Capital Equipment Protection: By eliminating large, solid clumps before they enter the fluid stream, the system actively prevents catastrophic mechanical damage to costly downstream process valves, reactors, and mixing tanks.
Rapid Dissolution: Once difficult powders (such as sodium chloride, ammonium sulfide, or complex media and buffers) pass through the system, they are transformed into flowable granules that seamlessly feed into downstream powder-liquid mixers for rapid, homogeneous dissolution.

GMP-Compliant & Versatile Integration

Built to adapt to strict regulatory environments and tight facility layouts:

Flexible Footprint: Designed as a highly convenient system that can be deployed as a stand-alone unit or installed directly in-line to connect seamlessly with existing reactors and mixing skids.
Strict Hygienic Execution: Manufactured to strict GMP standards with integrated Clean-In-Place (CIP) options, ensuring rapid decontamination between processing campaigns.
Explosion-Proof Safety: To handle volatile or highly reactive powders safely, the system is fully available in explosion-proof/ATEX-certified configurations.

Talk to an Industry Specialist

Our team understands GMP environments, classification requirements, and what your QA team needs to stay audit-ready.