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Semiconductor clean room grades

  • Author:Jason Peng

  • Cleanroom Engineering Technology Manager of Deiiang Company.

    Product R&D Manager of GDC Inc. Cleanroom Equipment Manufacturing Company.

    Executive Director of Guangdong Cleanroom Industry Association of China.

    Engaged in R&D of related products for 15 years, with rich relevant technical experience

  • 2024-12-25  |  Visits:

Clean rooms are essential environments in the semiconductor industry, ensuring that the manufacturing processes are not contaminated by airborne particles and other impurities. The cleanliness of these rooms is categorized based on specific standards, and the most commonly referenced guidelines come from the International Organization for Standardization

The Importance Of Cleanroom In The Semiconductor Industry

CleanRoom Classifications

The cleanliness of a semiconductor clean room is classified according to the number of particles per cubic meter at a specified size. The ISO 14644-1 standard is widely used to define these classifications. Clean rooms are categorized

  • ISO Class 1: Maximum of 10 particles ≥

  • ISO Class 2: Maximum of 100 particles ≥ 0.1 µm/m³

  • ISO Class 3: Maximum of 1

  • ISO Class 4: Maximum of 10,000 particles ≥ 0.1 µm/m³

  • ISO Class 5: Maximum of 100,000 particles ≥ 0.1 µm/m³

As the cleanliness class increases, the allowable number of particles decreases. This classification is critical, particularly in semiconductor manufacturing, where even a single particle can cause defects in microchips.

Importance of Cleanroom Grades

Maintaining the appropriate cleanroom grade is crucial for various reasons.

  • Product Quality: The primary goal of cleanroom environments is to ensure high-quality products. Contaminants can lead to defects, reducing yield and increasing costs.

  • Process Control: Clean rooms help maintain consistent manufacturing processes. Strict

  • Regulatory Compliance: Many semiconductor manufacturers must adhere to local and international regulations. Compliance with ISO standards not only ensures product quality but also enhances marketability

Cleanroom design and Operation

Designing and operating a cleanroom involves several critical elements.

Airflow and Filtration

The airflow in a cleanroom is designed to minimize particle accumulation. High-efficiency particulate air (HEPA) or

  • HEPA Filters: Capture 99.97% of particles ≥ 0.3 µm.

  • ULPA Filters: Capture 99.999%

The airflow pattern is typically unidirectional, creating a laminar flow that helps sweep away contaminants.

Materials and Equipment

  • Non-porous materials: These materials help prevent the accumulation of dust and other particles.

  • Smooth surfaces: Smooth surfaces

Deiiang, a leader in cleanroom equipment and solutions, provides specialized products that adhere to these stringent requirements. Their offerings include cleanroom furniture, air filtration systems, and contamination control solutions that ensure optimal cleanliness levels.

Monitoring and Maintenance

Regular monitoring of cleanroom environments is essential for maintaining the desired cleanliness standards. This includes:

  • Particle Counting: Regular particle counts should be performed to ensure compliance with the specified ISO class.

  • Air Quality Testing: Parameters such as temperature, humidity,

  • Routine Cleanliness Audits: Scheduled audits help identify any potential contamination sources and ensure ongoing compliance.

Training staff on cleanroom protocols is also vital. Employees must understand the importance of maintaining cleanliness and follow strict protocols when entering

Conclusion

In conclusion, the classification of semiconductor clean rooms according to ISO standards plays a pivotal role in the manufacturing process. As technology continues to advance, the demand for cleaner environments will only increase. Adhering to these standards not

Investing in high-quality cleanroom solutions, such as those provided by Deiiang, is essential for companies aimin.

References

  • iso 14644-1: Classification of air cleanliness

  • iso 14644-2: Monitoring and control of cleanrooms

  • ISO 14644-3: Test methods for cleanrooms

  • ISO 14644-4: Design and construction of cleanrooms

  • iso 14644-5: Operations and maintenance of cleanrooms

  • ISO 14698: Biocontamination control

  • Federal Standard 209E: Cleanroom classification (historical reference)

  • GMP Guidelines: Good Manufacturing Practices

By ensuring compliance with these standards and continuously improving cleanroom practices, semiconductor manufacturers can achieve the highest levels of product quality and reliability.

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