Pharmaceutical Fully automatic Candle Type Filter for Medicine Industry (SS 304, SS316l)

  • 0.5-800μm
  • candle filter cartridge
  • S.S 304, 316L, Carbon steel
  • 1 Year
  • 1-60m²
  • 1-200°C
  • Description
  • Video

Overview

Candle filters are widely used in the pharmaceutical industry. During drug production, they offer excellent corrosion resistance and high-temperature tolerance, meeting the demands of various chemical reagents and high-temperature environments.
Compared to traditional bag filters and manual plate filters, pharmaceutical candle filters achieve 100% automation, making them highly suitable for filtering flammable, toxic, and corrosive substances. The system enables automatic recovery and filtration without shutdown, effectively avoiding production interruptions and ensuring operational safety for personnel.

Key Advantages

  • Excellent corrosion resistance in a wide range of chemical fluids.
  • High temperature resistance.
  • High filtration precision, suitable for pharmaceutical fine filtration.
  • All filtering steps are automated.
  • Mobile and flexible design, short production cycles and frequent batch changes.
  • Easy operation for cleaning, drying and discharging filter cake.
  • Specification

    Model Cartridge QTY Cartridge Size (mm) Filtering Area (m²) Capacity (t/h) Housing Volume (L) Inlet Cake Discharging Outlet Total Height (mm)
    DZZS-1 7 90×500 1 2.2 140 DN25 DN150 1902
    DZZS-1.5 10 90×500 1.5 3.3 180 DN25 DN200 1928
    DZZS-2 7 90×1000 2 4.4 220 DN32 DN150 2402
    DZZS-3 10 90×1000 3 6.6 280 DN40 DN200 2428
    DZZS-4 14 90×1000 4 8.8 400 DN40 DN200 2502
    DZZS-6 19 90×1000 6 13.2 560 DN50 DN250 2578
    DZZS-8 24 90×1000 8 18 740 DN65 DN250 2644
    DZZS-12 40 90×1000 12 26 1200 DN65 DN300 2854
    DZZS-18 64 90×1000 18 40 1800 DN80 DN400 2904
    DZZS-30 106 90×1000 30 66 3000 DN100 DN500 3440
    DZZS-40 140 90×1000 40 88 3815 DN150 DN500 3560
    DZZS-60 190 90×1000 60 132 5700 DN150 DN500 3700

    Typical Application Scenarios

    • Separation of biomass from fermenter slurries.
    • Separation of precipitated solids in downstream processing lines.
    • Activated carbon treatment of liquid product streams.
    • Separation of heterogenous catalysts in hydrogenation reactions.
    • Filtration of crystalline products.
    • Capture of cell debris from both mammalian and bacterial cells.
    • Removal of precipitates from enzymes and plasma.
    • Protein fractions.
    • Phase separation in blood substitutes.
    • Crystal separation of injectable antibiotics.

    Selection Notes (Limitations)

    • Stringent validation and documentation requirements apply. Comprehensive material certificates, welding records, FAT/SAT documentation, and validation support must be provided.
    • Operational management demands strict adherence. Differential pressure, flow rates, and cleaning procedures require rigorous control to prevent compromised filtration performance or cross-contamination risks.

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