Polyethersulfone (PES) Capsule Filters - SF14918
PES capsule filters deliver the combination of high flow rates, low extractables, and validated retention performance that biopharmaceutical and laboratory workflows demand. Complementing this, PES membrane chemistry delivers broad pH compatibility from 1 to 14, supporting filtration of buffers, media, and cleaning solutions through a single capsule platform without material degradation. To this end, the outcome is simplified regulatory documentation and reduced contamination risk, with each single-use capsule providing a validated, traceable filtration event.
Key Polyethersulfone (PES) Membrane Characteristics
- The non-sterile capsule format offers a cost-effective option for applications where particle removal rather than sterility assurance is the primary filtration objective.
- Rated for operating pressures up to 75.4 psi, the capsule housing withstands the system pressures encountered in peristaltic pump, pressure vessel, and gravity-feed filtration configurations.
- 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.
- Single-membrane construction simplifies integrity test interpretation, as the bubble point and diffusion flow values correspond directly to the rated retention membrane without prefilter interference.
- The inherently hydrophilic PES membrane wets immediately on contact with aqueous solutions, eliminating alcohol pre-flush steps and reducing both startup time and solvent waste.
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.
- The sealed polypropylene housing is individually integrity-tested during manufacturing, verifying membrane installation and housing seal quality before the device leaves the production facility.
- Polypropylene capsule housing supports autoclave sterilization at 121 degrees Celsius and withstands gamma irradiation exposure, accommodating both user-sterilized and factory-sterilized device configurations.
- Polypropylene housing materials provide documented biocompatibility and low extractable profiles, supporting integration into pharmaceutical and food-processing filtration applications.
Whether your process requires sterilizing-grade retention for a 500-milliliter bench trial or clarification capacity for a 100-liter production batch, the right capsule filter configuration eliminates the compromises between throughput, retention, and operational simplicity. For laboratories processing cell culture media, buffers, or biological preparations, PES capsule construction delivers the combination of low binding, high throughput, and validated retention that your quality system depends on. Take control of your sample preparation variables and ensure that your data reflects the true nature of your work, rather than the quality of your consumables.
Sterilization Guidance
Supplied non-sterile, the polypropylene housing supports autoclave sterilization at 121 degrees Celsius for 20 minutes when aseptic filtration is required by the application protocol.
For more information about chemical compatibility, please review our Chemical Compatibility Chart.
- Bubble Point (psi)
- 29psi
- 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
- 0.5 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)
- 0.05
- Prefilter (Yes/No)
- No
- Sterility
- Nonsterile
- Sterilization
- Autoclavable at 121°C for 30 mins
- Vent (Yes/ No)
- Yes
- Weight
- 0.42
- Wettability
- Hydrophilic
- Reagent Filtration - Removal of particulates and contaminants from laboratory reagents and process solutions before downstream use.
- Buffer Processing - Large-volume filtration of pharmaceutical buffers and process solutions with broad pH compatibility across pH 1-14.
- Serum Processing - Capsule filtration of animal sera and biological supplements for cell culture and diagnostic reagent applications.
- Water Purification - Membrane-grade filtration of purified water and water-for-injection systems in pharmaceutical manufacturing facilities.
- 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.