HVAC

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Clean Room
Clean Room is a confined space where contamination control measures are in place, regulating not only airborne particulates but also environmental parameters such as temperature, humidity, indoor air pressure, and gas composition. They are categorized into industrial and medical applications and incorporate advanced cleanliness technologies along with various environmental control systems, forming a highly specialized energy-intensive facility.
Industrial Clean Room(ICR)
Industrial Clean Room is used to improve product quality and reliability, as well as to increase production yield, with airborne particles being the primary target of control. In addition to cleanliness, environmental conditions such as temperature, humidity, pressure, airflow, noise, and vibration must also be controlled as needed.
Classification Description
ICR Electronic Industry Semi-Conductor Product management in crystal growth, diffusion, photo etching, and metal deposition processes.
P.C.B Photography, Developing, Drying, Photomask Fabrication, Picturing, DP, Drying
Satelite Increase of reliability
Thin Film Film, Lamination/Adhesive Material, Aluminum Box Manufacturing, Flexible Packaging Material
Precision Industry Precision Machinery Aviation, Nautical Instruments, General Measuring Instruments, High-precision Switches using Mercury and Air
Optical Machinery Camera Assembly, Lens Manufacturing and Assembly, Shutter Assembly, Microfilm
Watches Assembly, Electronic Watch Manufacturing / Electro-Luminescence Production
Bio Clean Room(BCR)
The concept of the Bio Clean Room originated with the U.S. National Aeronautics and Space Administration (NASA) as a technology developed to prevent the transfer of microorganisms from Earth into space, and to avoid bringing extraterrestrial microorganisms back to Earth that could cause infections from previously unencountered microbes. This technology has since been applied in hospitals, pharmaceutical manufacturing, and other related fields.
Classification Reasons for CR Need Description
BCR Pharmaceutical Quality improvement
Accurate evaluation of drug efficacy
Regulation of microorganisms
Measures for preventing cross-contamination are particularly important
Legal regulations Animals must not be killed during experiments
Prevention of quality and taste changes
Production of products with long shelf life at room temperature
May be subject to GMP standards
Products with LONG-LIFE required
Areas handling hazardous substances are required Areas handling hazardous substances are required
Hospital Reducing infection risk for workers
Maintaining and extending life
Applied in cases with high infection risk and weak resistance
Difficult to objectively evaluate effectiveness
Protecting people lacking resistance to infections Installed mainly in general spitals
Five Principles of Cleanroom Management
Category Main Principle Implementation Examples
Preventing Prevent the inflow of dust into the clean room Install filters in supply lines
Prevent air leaks in ducts
Use double doors
Prohibiting Do not generate dust Exhaust contaminated air
Increase frequency of ventilation
Regular scheduled cleaning
Purging Immediately remove generated dust Use low-dust materials
Select equipment materials according to required class
Wear dust-proof clothing
Protecting Protect products from dust Designated work areas using clean benches
Clean storage locations
Providing Prepare dust removal equipment Air Shower, Pass Box
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