FS Series Square Vibrating Screen for Pharmaceutical Powder and Granule Screening
Equipment: FS
Classify powder or granule feeds on a square screening surface. The FS configuration is selected around the required fractions, feed rate and screen-deck arrangement. Specify the square vibrating screen as a vibratory sifter for the actual powder screening or granule screening duty. Particle size classification trials should check mesh blinding, screen loading and separation into the required fractions.
Product Overview
Classify powder or granule feeds on a square screening surface. The FS configuration is selected around the required fractions, feed rate and screen-deck arrangement.
Working Principle
The vibration motors drive the square screen body in a controlled reciprocating motion. Material travels across the screen surface, fines pass through the selected mesh, and oversize material leaves through a separate outlet.
Key Features
- Controlled vibration moves feed across a square screen.
- Selected mesh openings separate the required size fractions.
- Separate discharge paths handle fine and oversize material.
Suitable Materials
- Powders and granules requiring size classification.
- Material suitability should be confirmed through review of physical properties, moisture or solvent content, temperature sensitivity and the required final product condition.
Applications
Consider powder and granule classification, removal of oversize particles and preparation of sized feeds for downstream handling. Evaluate screen loading and blinding with the actual material.
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.
| Model | Production Capacity (kg/h) | Mesh Range (mesh) | Motor Power (kW) | Vibration Frequency (r/min) | Exciting Force (kN) | Outlet Height—Upper (mm) | Outlet Height—Middle (mm) | Outlet Height—Lower (mm) | Overall Dimensions (L×W×H) (mm) | Net Weight (kg) |
|---|---|---|---|---|---|---|---|---|---|---|
| FS-0.5M2-X | 450 | 2–150 | 0.2×2 | 1400 | 0–2.5×2 | 800 | 680 | 500 | 1300×770×1060 | 220 |
| FS-0.7M2-X | 650 | 2–150 | 0.2×2 | 1400 | 0–2.5×2 | 850 | 750 | 530 | 1700×680×1100 | 280 |
| FS-0.8M2-X | 750 | 2–150 | 0.2×2 | 1400 | 0–2.5×2 | 850 | 750 | 530 | 1600×830×1150 | 320 |
| FS-1.2M2-X | 1100 | 2–150 | 0.4×2 | 960 | 0–5×2 | 880 | 760 | 520 | 1900×980×1220 | 450 |
| FS-1.6M2-X | 1500 | 2–150 | 0.4×2 | 960 | 0.5×2 | 900 | 780 | 530 | 2200×1030×1250 | 620 |
| FS-2.0M2-X | 2000 | 2–150 | 0.75×2 | 960 | 0.5×2 | 900 | 780 | 530 | 2400×1130×1300 | 780 |
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
Specify mesh opening, the number of required fractions, feed bulk density and throughput. Review deck arrangement, screen access, dust containment and cleaning between product changes.
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 and Granule Screening
Define the feed particle distribution, selected mesh openings and required fine and oversize fractions. Test loading and mesh blinding on representative material, then confirm the discharge and cleaning arrangements for the pharmaceutical screening step.
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.