2 x 5m ISO 7 Softwall Cleanroom
Reference Price:US$3300.00-4500.00




Cleanroom
2 x 5m ISO 7 Softwall Cleanroom
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Summary
2 x 5m ISO 7 Softwall Cleanroom
Validation
Installation & Validation
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Cleanrooms Detail
An ISO 7 softwall cleanroom is a controlled environment designed to limit airborne particulate contamination to a specific level, defined by the ISO 14644-1 standard. In an ISO 7 cleanroom, the maximum allowable particle count is 352,000 particles per cubic meter for particles ≥0.5 micrometers.
Key Parameters and Standards
Air Quality:
352,000 particles/m³ (≥0.5 µm)
83,200 particles/m³ (≥1.0 µm)
Air Changes:Typically requires 30 to 60 air changes per hour, depending on the specific application.
Temperature: Usually maintained between 20°C to 22°C (68°F to 72°F).
Humidity: Typically kept between 30% to 60% relative humidity.
Applications
ISO 7 softwall cleanrooms are commonly used in various industries, including:
Pharmaceutical Manufacturing: Required for the production of sterile products and medications.
Biotechnology: Used in cell culture and research applications where contamination control is critical.
Electronics Manufacturing: Essential for the production of semiconductors and sensitive electronic components.
Medical Device Manufacturing: Ensures the cleanliness needed for the production of sterile devices.
These cleanrooms provide a flexible and cost-effective solution for industries that require stringent contamination control while allowing for easy configuration and scalability.
Cleanrooms Airflow
The airflow principles in an ISO 7 softwall cleanroom are essential for maintaining the desired cleanliness levels and controlling contamination. Here’s a brief overview of the key concepts involved:
Unidirectional Flow:
ISO 7 cleanrooms typically employ unidirectional airflow, where air moves in a consistent direction (usually from top to bottom or side to side). This design helps to sweep particles away from critical areas and minimizes stagnation, reducing the risk of contamination.HEPA Filtration:
High-Efficiency Particulate Air (HEPA) filters are crucial in maintaining cleanroom air quality. These filters remove at least 99.97% of particles ≥0.3 micrometers. In an ISO 7 cleanroom, air is drawn through these filters before being distributed throughout the space, ensuring that the air supplied is clean.Air Changes per Hour (ACH):
An ISO 7 cleanroom typically requires 30 to 60 air changes per hour. This rate ensures that the air within the cleanroom is regularly replaced, reducing the concentration of airborne particles and maintaining overall air quality.Positive Pressure:
The cleanroom is maintained at a positive pressure relative to adjacent areas. This pressure differential helps prevent unfiltered air from entering the cleanroom, further ensuring that contamination is kept to a minimum.Return Air Path:
Air is usually exhausted from the cleanroom through return air grilles, which are strategically placed to enhance airflow patterns. The return air is then filtered and conditioned before being reintroduced into the cleanroom, creating a continuous circulation loop.
By understanding and implementing these airflow principles, ISO 7 softwall cleanrooms can effectively maintain the required cleanliness levels necessary for various sensitive applications.
Cleanrooms Installation
ISO 7 Softwall Cleanrooms Installation Steps
Site Preparation: Clean the area and ensure a suitable, level floor.
Framework Construction: Build the support structure for softwall panels.
Wall Installation: Attach softwall panels securely to minimize gaps.
Ceiling and Lighting: Install cleanroom-compatible ceiling panels and lighting fixtures.
Airflow System Setup: Install HEPA filters, ductwork, and air supply vents.
Pressure and Temperature Control: Set up HVAC systems to maintain desired conditions.
Testing and Validation: Conduct airflow and particle count tests to ensure compliance with ISO 7 standards.
Final Inspection: Verify installation and obtain certification of cleanliness.
These steps ensure the effective installation of an ISO 7 softwall cleanroom.
Cleanrooms Testing
Air Cleanliness: The clean room must be able to control the number of particles and microorganisms in the air so that the air cleanliness meets the specified requirements.
Temperature and humidity: The clean room needs to control the indoor temperature and humidity to adapt to different production needs. Temperatures typically need to be controlled at 20-24°C and relative humidity at 45-60%.
Lighting: Clean rooms need to provide adequate lighting to ensure that staff can clearly see the objects being operated. In general, the illumination should be greater than 300 lux.
Pressure difference: In order to prevent external contamination into the clean room, need to maintain a certain indoor and outdoor pressure difference. Generally speaking, the indoor pressure should be slightly higher than the outdoor pressure.
Noise: Noise at work in the clean room should be kept within permissible limits to protect the physical and mental health of staff.
FAQ
1. What is a modular cleanroom?
A modular cleanroom is a pre-engineered and prefabricated system that can be easily assembled and customized to meet specific contamination control requirements. These cleanrooms are designed to be flexible, allowing for quick installation and modifications as needed. They are often used in industries such as pharmaceuticals, biotechnology, and electronics.
2. How do you handle waste in a cleanroom?
Handling waste in a cleanroom requires strict protocols to maintain cleanliness and prevent contamination. Waste is typically categorized into:
Non-hazardous waste
Hazardous waste
Biohazardous waste
Each type of waste is placed in designated containers, clearly labeled, and disposed of according to regulatory guidelines. Regular training for personnel is essential to ensure compliance with waste management procedures.
3. How do you monitor cleanroom conditions?
Monitoring cleanroom conditions involves using various sensors and systems to track environmental parameters such as temperature, humidity, and particulate levels. Continuous monitoring is essential to ensure that the cleanroom remains within specified limits, and alarms can be set to alert personnel of deviations. Data logging systems are often employed to maintain records for compliance and quality assurance purposes.
4. What are the best practices for cleanroom maintenance?
Best practices for cleanroom maintenance include regular cleaning schedules and the use of appropriate cleaning agents that do not leave residues. Key practices are:
Conducting regular inspections of equipment and surfaces
Training personnel on proper gowning procedures
Monitoring environmental conditions consistently
By following these practices, the integrity of the cleanroom environment can be upheld, minimizing contamination risks.
5. What is the purpose of cleanroom monitoring systems?
The purpose of cleanroom monitoring systems is to ensure that the environmental conditions within the cleanroom remain stable and within defined parameters. These systems help track variables such as temperature, humidity, and particle counts, which are critical for maintaining product quality and compliance with industry standards. Additionally, they provide real-time alerts for any deviations, allowing for prompt corrective actions.
6. What is the impact of temperature fluctuations in cleanrooms?
Temperature fluctuations in cleanrooms can lead to several negative impacts, including compromised product integrity and potential contamination. Variability in temperature may affect the chemical stability of materials, result in condensation, or alter the performance of sensitive equipment. Therefore, maintaining a consistent temperature is crucial for ensuring the reliability and safety of processes conducted within the cleanroom.
7. How is the layout of a cleanroom determined?
The layout of a cleanroom is determined by several factors, including the specific processes that will take place, equipment requirements, and personnel workflow. Key considerations include:
Airflow patterns
Equipment placement
Access routes for personnel and materials
A well-thought-out layout is essential for minimizing contamination risks and optimizing operational efficiency.
8. What is the process of commissioning a cleanroom?
The commissioning process of a cleanroom involves a series of steps to ensure that the facility meets all design specifications and operational requirements. It typically includes:
Verification of construction and installation
Performance testing of HVAC systems
Environmental testing to ensure compliance with cleanliness standards
This process is critical to confirm that the cleanroom is ready for use and meets regulatory requirements.
9. What types of flooring are suitable for cleanrooms?
Suitable flooring options for cleanrooms include:
Vinyl flooring
Epoxy resin
Rubber flooring
These materials are selected for their durability, chemical resistance, and ease of cleaning, which are essential for maintaining the cleanliness and integrity of the cleanroom environment.
10. How do you prevent static electricity in a cleanroom?
Preventing static electricity in a cleanroom involves several strategies, including:
Using anti-static flooring materials
Implementing ionization systems
Ensuring personnel wear anti-static garments
These measures help minimize the risk of static discharge, which can harm sensitive electronic components and compromise product integrity.
11. How long does it take to install a cleanroom?
The installation time for a cleanroom can vary significantly depending on the size and complexity of the design. On average, it takes between several weeks to a few months to complete the installation. Factors such as customization requirements and contractor efficiency can influence the overall timeline.
12. What is the typical size of a modular cleanroom?
The typical size of a modular cleanroom can range widely based on the application and industry requirements. Modular cleanrooms can be as small as a few hundred square feet to several thousand square feet. Their flexibility allows for customization according to specific needs, making them suitable for various processes and equipment configurations.
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