SteriSpace Advanced Air & Chemical Sterilization System
SteriSpace Air & Chemical Sterilization Technology
SteriSpace Air Sterilization Technology is a patented, turnkey system engineered for healthcare, industrial, and government applications. Its compressive-heating technology inactivates airborne pathogens—including viruses, bacterial spores, and mold—achieving lab-tested kill rates exceeding 99.9999%. Units are scalable to treat airflows from tens to thousands of CFM and can integrate with HVAC systems or operate standalone. Optional chemical catalyst modules reduce VOCs and pollutants (manufacturer-reported). Positive or negative pressure configurations, rapid setup, minimal consumables, and mobility make SteriSpace a safe, efficient, and flexible solution that enhances biosafety, biosecurity, and operational efficiency.
Key Features:
- Patented compressive-heating air sterilization technology
- Airborne pathogen kill rate >99.9999% (lab-tested)
- Eliminates pathogens smaller than 0.3 microns, surpassing HEPA filtration
- Optional chemical catalyst for VOC and environmental pollutant removal (manufacturer-reported)
- Scalable for hundreds to thousands of CFM airflow
- Standalone, HVAC-integrated, mobile, or tent deployment
- Positive or negative pressure configuration options
- Fully insulated, quiet, energy-efficient, low-maintenance operation
- Eliminates biohazard exposure risk to workers
Technical Specifications – SteriSpace Advanced Air Sterilization Device
| Specification | Details |
|---|---|
| Model Number | SteriSpace SS Model line |
| Applications | Air sterilization; standalone or integrated with new/existing HVAC systems |
| Pathogen Kill Rate | >99.9999% (lab-tested), log 6 reduction |
| Compressive Heat Magnitude | Up to 464 °F (240 °C) |
| Airflow Capacity | 100–10,000 CFM |
| Dimensions (L×W×H) | Variable based on model/capacity |
| Weight | Variable |
| Power Requirements | 3 Phase or 1 Phase, 60 Hz, 208–240 VAC or 440–480 VAC |
| Noise Level | Typically <75 dB |
| Included Items | Electric service disconnect, mechanical flanged connections, finger-safe cable assemblies on mobile/shelter systems |
| Deployment Options | Standalone, HVAC-integrated, mobile, tent/shelter, positive/negative room pressure capable |
| Maintenance | Annual lubrication only; no filters required |
| Certifications | Not specified by MFR (verification needed) |
Technical Specifications – SteriSpace Electric Recuperative Catalytic Thermal Oxidizer (CATOX)
| Specification | Details |
|---|---|
| Model Number | SteriSpace CC Model line |
| Applications | Ethylene Oxide (EtO) and Propylene Oxide (PPO) abatement systems; process and fugitive fumes abatement |
| EtO/PPO Reduction | EtO reduced to 5 PPB residual; PPO to 10 PPB residual |
| Compressive Heat Magnitude | As required for total destruction |
| Airflow Capacity | 100–5,000 CFM |
| Dimensions (L×W×H) | Variable based on model/capacity |
| Weight | Variable |
| Power Requirements | 3 Phase or 1 Phase, 60 Hz, 208–240 VAC or 440–480 VAC |
| Noise Level | Typically <75 dB |
| Included Items | Electric service disconnect, mechanical flanged connections |
| Deployment Options | Integrates with Water Balancer/Peak Shaver, Wet or Dry Scrubbers |
| Maintenance | Catalyst change every 5 years; annual lubrication required; no filters used |
| Certifications | Not specified by MFR (verification needed) |
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Frequently Asked Questions
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What is the measured or expected EO (or PPO) concentration at the source?
What is the measured or expected EO (or PPO) concentration at the source?
Provide concentration in ppm (parts per million). Indicate whether this is peak, typical, or maximum design concentration.
Why: Determines required dilution, safety measures for flammability (LEL), and CATOX sizing.
What is the volumetric flow rate of the EO/air stream to be abated? (CFM)
What is the volumetric flow rate of the EO/air stream to be abated? (CFM)
Give the flow in CFM at the stated concentration and indicate temperature/pressure if non-standard.
Why: Critical for selecting unit model and catalyst sizing.
What is the LEL (lower explosive limit) safety target or operating practice for the process?
What is the LEL (lower explosive limit) safety target or operating practice for the process?
State the %LEL or ppm threshold you will maintain (e.g., keep below ¼ LEL / 7,000 ppm for small-room sterilizers).
Why: Impacts required dilution strategy, use of air injection or water balancer, and safe transport to thermal oxidizer.
What are the inlet and exhaust duct/piping sizes and connection details?
What are the inlet and exhaust duct/piping sizes and connection details?
Specify diameter (inches), material, flange type, and required insertion depth or transition pieces. Include inlet/outlet orientation.
Why: Ensures mechanical fit, reduces pressure-drop surprises, and confirms exhaust stack compatibility.
What are the physical installation conditions and delivery logistics?
What are the physical installation conditions and delivery logistics?
Where will the unit be located (outside ground level, rooftop, inside mechanical room, mobile trailer)? Provide delivery address, dock availability, and any site access restrictions.
Why: Defines shipping method, crane/rigging needs, and onsite installation plan.
How far is the abator mounting point from the fume collection/point source?
How far is the abator mounting point from the fume collection/point source?
Give straight-line distance and duct run length (feet), number of bends, and any elevation changes.
Why: Affects fan sizing, pressure requirements, and ductwork design.
What electrical service is available on site?
What electrical service is available on site?
Confirm 3-phase or single-phase, voltage (208/230 V or 460/480 V), frequency (60 Hz), and available ampacity at the installation point. Note if disconnects are provided.
Why: Determines power configuration, transformer needs, and whether a site electrical upgrade is required.
What are the room or facility dimensions and ventilation context?
What are the room or facility dimensions and ventilation context?
For fugitive fume abatement, provide room L×W×H, occupancy, and typical ventilation (ACH) or existing HVAC integration points.
Why: Needed when sizing units for ambient gassing scenarios and determining how much air must be treated.
What ancillary abatement or pretreatment equipment is present or planned?
What ancillary abatement or pretreatment equipment is present or planned?
List any scrubbers, water balancer (bubbler), acid scrubber, HEPA, peak shaver, or wet/dry scrubbers your site uses or will use upstream/downstream.
Why: Helps specify integration points and whether the CATOX should be used standalone or in series with pretreatment.
What operational, maintenance, and regulatory constraints apply?
What operational, maintenance, and regulatory constraints apply?
Provide expected runtime (hours/day), required maintenance window, local emissions/permitting limits, and any certification needs. Also indicate whether remote monitoring or alarm integration is required.
Why: Influences catalyst selection (life expectancy), maintenance schedule, permitting assistance, and control/interface features.