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SteriSpace Advanced Air & Chemical Sterilization System

SteriSpace Air Sterilization Technology
 
 





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Product Code: NSSS

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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

Features
Q: What is the measured or expected EO (or PPO) concentration at the source?
  • A. 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.

Q: What is the volumetric flow rate of the EO/air stream to be abated? (CFM)
  • A. 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.

Q: What is the LEL (lower explosive limit) safety target or operating practice for the process?
  • A. 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.

Q. What are the inlet and exhaust duct/piping sizes and connection details?
  • A. 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.

Q: What are the physical installation conditions and delivery logistics?
  • A. 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.
Q: How far is the abator mounting point from the fume collection/point source?
  • A. 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.
Q: What electrical service is available on site?
  • A. 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.
Q: What are the room or facility dimensions and ventilation context?
  • A. 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
Q: What ancillary abatement or pretreatment equipment is present or planned?
  • A. 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.
Q: What operational, maintenance, and regulatory constraints apply?
  • A. 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.

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