Polyethersulfone (PES) Capsule Filters - SF14991
Ultra-low protein binding and broad pH compatibility from 1 to 14 make PES capsule filters the preferred membrane choice for processing biological solutions at production scale. Furthermore, the pleated PES membrane pack maximizes effective filtration area within the capsule housing, sustaining high flow rates through large batch volumes while inherent hydrophilicity ensures immediate wetting without alcohol pre-treatment. The outcome is a validated filtration barrier that arrives ready for process integration, supporting the single-use manufacturing strategies adopted by modern pharmaceutical and biotechnology facilities.
Key Polyethersulfone (PES) Membrane Characteristics
- The 80 degree Celsius temperature limit ensures reliable capsule performance for ambient and moderately heated filtration applications.
- The asymmetric pore structure of PES membranes captures contaminants at the upstream surface while maintaining open downstream channels, extending capsule throughput before reaching differential pressure limits.
- Non-sterile capsules support autoclave sterilization where the membrane and housing materials permit, allowing users to prepare devices according to their own validated sterilization protocols.
- PES membrane construction supports integrity testing by forward flow, bubble point, or pressure decay methods, providing the post-use verification required by pharmaceutical quality systems.
- Capsule holdup volume of 60 milliliters represents the fluid retained within the device after filtration, an important factor when calculating yield for high-value pharmaceutical products.
Key Capsule Construction Features
- Single-use polypropylene capsule construction eliminates cleaning validation requirements, reducing the regulatory burden and turnaround time associated with reusable stainless steel filter housings.
- Polypropylene capsule housing supports autoclave sterilization at 121 degrees Celsius and withstands gamma irradiation exposure, accommodating both user-sterilized and factory-sterilized device configurations.
- The sealed polypropylene housing is individually integrity-tested during manufacturing, verifying membrane installation and housing seal quality before the device leaves the production facility.
- Thermally fused polypropylene construction eliminates adhesives, binders, and O-rings from the fluid path, reducing extractable contamination and simplifying material qualification.
As batch volumes and regulatory expectations continue to grow, your capsule filter selection becomes a process design decision that affects sterility assurance, product recovery, and operational cost per liter filtered. To meet this need, if your process involves aqueous biologicals, the ultra-low protein binding and broad pH compatibility of PES membrane construction protect your product while sustaining the flow rates your batch schedule requires. Make the decision for consistency and reliability, ensuring that your laboratory maintains its reputation for high-quality, error-free output.
Sterilization Guidance
Non-sterile delivery accommodates applications where sterility is not required, while the all-polypropylene construction provides the option for autoclave sterilization when aseptic processing is specified.
For more information about chemical compatibility, please review our Chemical Compatibility Chart.
- Bubble Point (psi)
- 58psi
- Compliance Standards
- ISO 9001
- Connection Type
- 1/4 in. MNPT
- Construction
- Polypropylene
- Diameter
- 72mm
- Dimensions
- 72mm x 115mm
- Filling Bell (Yes/ No)
- No
- Filtration Area
- 1000cm²
- Flow Rate
- 1.2 L/min at 0.1 bar
- Holdup Volume
- 60mL
- Inlet Connection
- 1/4 in. MNPT
- Length
- 115mm
- Material
- PES
- Max Batch Volume
- <50L
- Maximum Operating Pressure
- 75.4psi
- Maximum Operating Temperature (°C)
- 80°C
- Outlet Connection
- 1/4 in. MNPT
- Pack Count
- 1
- Pore Size (µm)
- 0.1
- Prefilter (Yes/No)
- No
- Sterility
- Nonsterile
- Sterilization
- Autoclavable at 121°C for 30 mins
- Vent (Yes/ No)
- Yes
- Weight
- 0.39
- Wettability
- Hydrophilic
- Serum Processing - Capsule filtration of animal sera and biological supplements for cell culture and diagnostic reagent applications.
- Biologics Protection - Ultra-low protein binding preserves antibody and growth factor concentrations through the membrane retention step.
- Process Intermediates - In-line capsule filtration of pharmaceutical intermediates with validated retention and low adsorptive losses.
- Buffer Processing - Large-volume filtration of pharmaceutical buffers and process solutions with broad pH compatibility across pH 1-14.
- Reagent Filtration - Removal of particulates and contaminants from laboratory reagents and process solutions before downstream use.
- Water Purification - Membrane-grade filtration of purified water and water-for-injection systems in pharmaceutical manufacturing facilities.