Pharmaceutical Equipment / Pulverizer Unit
High-Efficiency Pulverizer Unit for Pharmaceutical Powder Processing
Equipment: Pulverizer Unit
An integrated pulverizer unit brings feeding, mechanical size reduction and powder collection into one processing arrangement. The required system scope depends on the feed and product handling needs. For powder processing, review the pulverizer unit and powder collection stages together. Particle size reduction by impact grinding should be assessed against the actual feed, required outlet distribution and acceptable temperature rise.
Product Overview
An integrated pulverizer unit brings feeding, mechanical size reduction and powder collection into one processing arrangement. The required system scope depends on the feed and product handling needs.
Working Principle
Feed enters a high-speed chamber where impact and cutting reduce particle size. The resulting powder and conveying air move through cyclone and bag-collection stages to separate and collect the product.
Key Features
- Mechanical size reduction is integrated with collection equipment.
- Cyclone and bag stages separate product from the conveying air.
- The feed, mill and collection arrangement are selected as one system.
Suitable Materials
- Dry feeds that are compatible with the selected impact and cutting mechanism.
- Assess the actual material properties, moisture or solvent content, temperature limits and required finished-product condition before selecting the machine.
Applications
Consider integrated powder preparation where both size reduction and product recovery must be specified. Review powder handling and collection performance along with the mill itself.
Review our industry applications and confirm your process duty with QUANPIN.
Technical Parameters
On smaller screens, swipe the table sideways to view all models and values.
| Item | Unit | 20B | 30B | 40B | 60B |
|---|---|---|---|---|---|
| Production Capacity | kg/h | 60–150 | 100–300 | 160–800 | 500–1500 |
| Main-Shaft Speed | r/min | 4500 | 3800 | 3400 | 2800 |
| Feed Particle Size | mm | 6 | 10 | 12 | 15 |
| Pulverized Particle Size | mesh | 60–150 | 60–120 | 60–120 | 60–120 |
| Pulverizer Motor Power | kW | 4 | 5.5 | 11 | 15 |
| Dust-Extraction Fan Power | kW | 1.5 | 1.5 | 1.5 | 2.2 |
| Weight | kg | 250 | 320 | 550 | 680 |
| Main-Unit Dimensions (L×W×H) | mm | 550×600×1250 | 600×700×1450 | 800×900×1550 | 1000×900×1680 |
| Complete-Unit Dimensions (L×W×H) | mm | 1100×600×1650 | 1200×650×1650 | 1350×700×1700 | 1550×1000×1750 |
Confirm the selected configuration and material duty before ordering. Final dimensions, options and supply scope are recorded in the approved technical documents.
Selection and Configuration
Provide material hardness, moisture, feed size, target fineness and required rate. Confirm temperature limits, collection points, filter access, cleaning needs and material-specific protection requirements.
For pharmaceutical installations, specify product-contact materials, containment, cleaning procedures, controls and documentation requirements. These are project requirements to be agreed, rather than an automatic claim of certification.
Frequently Asked Questions
What is this equipment used for?
Which material information should be supplied?
How should the configuration be verified?
Agree a representative feed, output requirement and acceptance method with QUANPIN. Review particle-size distribution, product recovery, temperature limits and cleanability as applicable to the selected process.
Request Pricing & Specifications
Send your material name, feed condition, required throughput, target particle range and cleaning requirements.
Application Review: Pharmaceutical Powder Processing
Review the feed consistency and the required outlet particle distribution. Define the grinding, cyclone and bag-collection interfaces together, and check product recovery, cleaning access and temperature rise with representative material.
For pharmaceutical process evaluation, consult FDA process validation guidance.
For an active-ingredient application, review the equipment and documentation topics in FDA Q7A guidance.
For pharmaceutical cleaning requirements, consult the FDA equipment and cleaning questions.
Review the actual powder characteristics using the HSE safe handling of combustible dusts.
Include moving-part access in the installation review using HSE work equipment and guarding guidance.
Discuss Your
Processing Requirements.
Share your material, particle-size target and processing rate with QUANPIN to discuss an equipment configuration.