0.04 µm
Fine membrane configuration for applications requiring a smaller documented pore-size option. Final suitability depends on required retention performance and process validation.
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The SIP PTFE capsule filter is a compact, self-contained membrane filtration assembly designed for processes requiring steam-in-place (SIP) sterilisation. With a hydrophobic PTFE membrane configuration, it is particularly suited to sterile air, process gas, tank vent and bioprocess filtration applications in pharmaceutical and biotechnology environments.
The SIP-capable capsule format combines membrane filtration and housing in one assembly and is designed to remain integrated into the process during steam sterilisation procedures. This can simplify sterile gas and vent filtration installations compared with separate cartridge-and-housing systems.
| Filter type | Steam-in-place compatible membrane capsule filter |
|---|---|
| Membrane | PTFE membrane configuration |
| Membrane behaviour | Hydrophobic, suitable for air, gas and vent filtration |
| Media support | Polypropylene |
| End caps | Polypropylene |
| Inner core | Polypropylene |
| Outer cage | Polypropylene |
| Documented pore sizes | 0.04, 0.1, 0.2 and 0.45 µm |
| Capsule length options | 2.5" and 5" |
| Nominal length – 2.5" | Approx. 84 mm |
| Nominal length – 5" | Approx. 159 mm |
| Vent options | Staubli or hose-barb configuration |
| Process connection | Sanitary flange connection available depending on configuration |
| Integrity testing | Designed for connection to an automatic integrity-testing system |
| Biological safety | Selected component materials meet USP Class VI-121°C requirements for plastics |
| Material compliance | Documented FDA 21 CFR and EU 10/2011 food-contact material compliance |
Configuration note: pore size, membrane grade, connection arrangement and validation requirements should be confirmed for the exact capsule configuration. A nominal pore size alone does not establish sterilizing-grade performance for every configuration.
A steam-in-place capsule filter is designed to remain connected to the process system while the filtration assembly is exposed to a steam sterilisation procedure. This is especially useful in pharmaceutical and biotechnology systems where removing and reinstalling a filter between sterilisation cycles is undesirable.
The SIP capsule construction provides a compact alternative to a separate membrane cartridge installed inside a stainless-steel filter housing, particularly for smaller process lines, pilot installations and critical vent or gas filtration points.
PTFE membrane is naturally hydrophobic. For gas and vent applications this helps maintain gas flow while resisting penetration by liquid water under suitable operating conditions.
This behaviour makes PTFE particularly relevant for applications such as sterile air supply, tank and vessel venting, fermentation gas filtration and controlled gas exchange in pharmaceutical and biotechnology processes.
The documented SIP capsule platform supports several membrane pore-size configurations rather than only one fixed 0.2 µm option.
Fine membrane configuration for applications requiring a smaller documented pore-size option. Final suitability depends on required retention performance and process validation.
Fine PTFE membrane option for critical air, gas and vent filtration where a 0.1 µm configuration is specified.
Widely relevant to critical pharmaceutical gas and vent filtration. Where sterilizing-grade performance is required, the exact grade and supporting validation documentation must be confirmed.
A 0.45 µm configuration is also documented for the SIP capsule platform and may be considered where the required retention level permits a larger pore size.
Two compact capsule lengths are documented for this SIP platform: 2.5 inches and 5 inches.
| 2.5" capsule | Approx. 84 mm nominal length. Suitable where compact installation space and lower process-scale requirements are important. |
|---|---|
| 5" capsule | Approx. 159 mm nominal length. Provides a larger capsule format for applications requiring increased filtration capacity. |
Final capsule size should be selected from the required gas or liquid flow, pressure drop, process conditions and validation requirements rather than physical length alone.
For pharmaceutical and biotechnology filtration, membrane selection is only part of the specification. The materials, sterilisation approach and ability to verify filter integrity are also important.
Where a regulated pharmaceutical process requires validated sterile filtration, request the documentation applicable to the exact membrane grade, pore size and capsule configuration selected.
Filter integrity verification is important in critical membrane filtration processes because it provides a non-destructive way to check whether the installed membrane assembly remains within its defined integrity limits.
The SIP capsule design includes configurations that can be connected to an automatic integrity tester. The appropriate test method and acceptance limits depend on the exact membrane grade and pore-size configuration.
Filtra International also supplies membrane filter integrity testing equipment for pharmaceutical and biotechnology filtration systems.
| SIP PTFE capsule | Standard PTFE capsule | |
|---|---|---|
| Primary design objective | Integration into systems requiring steam-in-place procedures | Compact gas, vent, solvent and laboratory filtration |
| Membrane | Hydrophobic PTFE configuration | Hydrophobic PTFE |
| Typical use | Critical sterile air, gas and process vent filtration | Gas, vent, solvent and general PTFE capsule filtration |
| Integrity testing | Configuration supports connection to automatic integrity tester | Depends on selected capsule configuration |
Correct selection should start with the process conditions rather than the pore size alone.
Send us your process gas or liquid, required pore size, flow rate, sterilisation procedure and connection requirements. We can help determine whether an SIP PTFE capsule, standard PTFE capsule or another membrane configuration is more appropriate.
A SIP PTFE capsule filter is a self-contained membrane filter designed for process systems using steam-in-place sterilisation. The PTFE configuration is particularly suited to critical air, gas and vent filtration.
Documented pore-size options include 0.04 µm, 0.1 µm, 0.2 µm and 0.45 µm. The appropriate rating depends on the retention requirement and exact filter grade.
Yes. A 0.2 µm configuration is documented. Where validated sterilizing-grade performance is required, the supporting validation documentation for the exact configuration should also be confirmed.
The documented SIP capsule range includes 2.5-inch and 5-inch configurations, with nominal lengths of approximately 84 mm and 159 mm respectively.
PTFE is hydrophobic, allowing air and gas to pass through the membrane while resisting penetration by liquid water under suitable operating conditions. This makes it useful for sterile gas and process vent filtration.
Yes. The documented SIP capsule design supports connection to an automatic integrity-testing system. Test parameters and acceptance limits depend on the selected membrane configuration.
The documented capsule platform includes Staubli and hose-barb vent configurations. Final connection arrangement depends on the selected capsule.
The documented capsule materials include polypropylene support, end-cap, core and cage components, with selected materials meeting USP Class VI-121°C biological-safety requirements. Food-contact material compliance is also documented against relevant FDA 21 CFR and EU 10/2011 requirements.
The SIP capsule is specifically intended for processes requiring steam-in-place sterilisation. A standard PTFE capsule is generally used for compact gas, vent, solvent and laboratory filtration where an SIP-capable housing design is not required.
Selecting the correct filtration solution often requires verification under real process conditions. Filtra International supports this process through several practical testing and validation options.
• Filter samples – available for compatibility and performance checks in existing filter housings.
• Full-scale filter housing rental – for temporary installations or process evaluation.
• Laboratory and pilot-scale filtration units – enabling controlled testing before full implementation.
• Application testing by our team – customers may send product samples for filtration trials and performance evaluation.
These options allow process validation before committing to a permanent installation.
Share a few details about your process and our team can assist with product selection and sizing.
Typical parameters include:
• Flow rate
• Particle size or filtration rating
• Temperature and pressure
• Chemical composition of the media