Case Study of Dust Collector Filtration System for Pharmaceutical Tablet Production Line
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Case Study of Dust Collector Filtration System for Pharmaceutical Tablet Production Line

The original dust removal equipment featured low filtration precision, easy filter clogging and short service life, resulting in unstable indoor clean air quality and frequent production halt for equipment cleaning. To resolve these issues, the enterprise upgraded the central dust collector system, adopting customized filter bags and supporting filter cages to achieve efficient, stable and sterile dust purification, fully complying with pharmaceutical GMP production requirements.
Case Study of Dust Collector Filtration System for Pharmaceutical Tablet Production Line
Case Details

Case Study of Dust Collector Filtration System for Pharmaceutical Tablet Production Line

  1. Project Background

A GMP-certified pharmaceutical enterprise specializes in the mass production of oral solid tablets, including granulation, tableting, coating and packaging processes. The tablet production line generates a large amount of fine medicinal powder dust during raw material crushing, wet granulation drying and high-speed tableting operations. Uncontrolled dust not only causes raw material waste and cross-contamination between different batches of tablets but also fails to meet pharmaceutical clean production standards. The original dust removal equipment featured low filtration precision, easy filter clogging and short service life, resulting in unstable indoor clean air quality and frequent production halt for equipment cleaning. To resolve these issues, the enterprise upgraded the central dust collector system, adopting customized filter bags and supporting filter cages to achieve efficient, stable and sterile dust purification, fully complying with pharmaceutical GMP production requirements.

  1. Working Conditions and Core Equipment Specifications

The upgraded dust removal system is dedicated to dust collection and purification in pharmaceutical tablet production workshops. It adapts to low-temperature, dry and sterile clean workshop environments. All filter accessories meet pharmaceutical-grade purification standards. The detailed working conditions, filter bag and filter cage technical parameters are listed in the table below.

Category

Parameter Item

Specific Specification

Working Conditions

Dust Medium

Tablet raw material powder, microcrystalline cellulose, starch fine dust

Working Temperature

18–45℃ (normal temperature clean workshop)

Operating Wind Pressure

0.2–0.4 MPa negative pressure

Air Treatment Volume

3000–3500 m³/h

Filtration Requirement

Intercept fine dust ≥0.3μm, workshop dust emission ≤10mg/m³

Dust Collector Filter Bag

Filter Material

Pharmaceutical-grade PTFE membrane-coated polyester

Filtration Precision

0.3μm high-efficiency filtration

Size Specification

Φ130mm×2000mm standard round bag

Performance Characteristics

Anti-static, dust-free, easy ash cleaning, hydrolysis resistance, GMP compliant

Filter Cage Specifications

Cage Material

Low-carbon steel galvanized / 304 stainless steel optional

Structure Design

Integral one-piece structure, 12 longitudinal wires

Matching Size

Adapt to Φ130mm filter bag, fully fitted support

Surface Treatment

Smooth galvanized coating, no burrs, anti-corrosion, no powder falling

  1. System Filtration Principle

The system adopts negative pressure pulse jet dust removal technology suitable for pharmaceutical production. Under stable negative pressure, the dust-containing air generated from tablet production processes is sucked into the dust collector box. When passing through the PTFE membrane filter bag, fine medicinal dust is intercepted on the outer surface of the filter bag, while clean air penetrates the filter medium and is discharged up to standard. The matched filter cage provides full three-dimensional support for the filter bag, preventing bag shrinkage, deformation and air leakage under negative pressure. The regular pulse jet cleaning system automatically blows off the dust accumulated on the bag surface, ensuring long-term stable filtration resistance and avoiding blockage. The smooth and burr-free cage structure effectively prevents filter bag wear and damage, eliminating the risk of metal debris mixing into pharmaceutical materials.

  1. Operation Effects and Production Benefits

After three months of formal operation, the upgraded dust filtration system achieves excellent purification effects. The workshop air cleanliness meets Class D pharmaceutical clean workshop standards, with exhaust dust concentration stably below 8mg/m³. The PTFE membrane filter bag features ultra-low adhesion, realizing efficient automatic ash cleaning and extending the service cycle to 8–12 months, greatly reducing replacement and maintenance costs. The standardized filter cage effectively protects the filter bag, eliminating bag damage and air leakage failures. Meanwhile, centralized dust collection reduces tablet raw material loss, avoids cross-batch contamination, and improves the pass rate of tablet appearance and purity. The fully sealed dust removal structure also eliminates workshop dust floating, optimizing the production environment and passing GMP regular inspection smoothly.

  1. Conclusion

This customized dust collector filtration solution fully adapts to the clean and sterile production characteristics of pharmaceutical tablet lines through precise matching of filter bag and cage parameters. The high-precision dust removal, stable operation and GMP-compliant performance solve the common dust pollution and equipment instability problems in oral solid tablet production. The system has simple maintenance, low operating cost and high safety, which can be widely promoted in pharmaceutical granulation, tableting and powder processing workshops, providing reliable technical support for standardized and clean pharmaceutical production.

 

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