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Cleanrooms in Printing and Packaging

The printing and packaging industry has evolved significantly with the progress of society. This transformation has ushered in a new era, where large-scale printing equipment finds its home in clean and controlled environments. The integration of purification practices into these industries has yielded substantial benefits, elevating product quality and drastically improving product qualification rates.

1. The Vital Role of Cleanrooms

In both printing and packaging, cleanrooms are pivotal. They meticulously control parameters like temperature, humidity, and the presence of dust particles, directly impacting product quality and pass rates. The packaging industry, in particular, encompasses two critical aspects: food packaging and pharmaceutical packaging. These domains have stringent requirements concerning environmental conditions, airborne particle levels, and water quality. Equally important are standardized operating procedures for production personnel.

2. The Impact of Dust-Free Spraying

Dust-free spraying, a specialized production workshop enclosed by steel sandwich panels, effectively combats product contamination from the surrounding air environment. This technology significantly reduces the defect rate of products in the spraying area. The advantages extend to various products, including TV/computer casings, mobile phone shells, DVD/VCD, game consoles, video recorders, PDA handheld computers, camera casings, audio equipment, hairdryers, toys, and more.

The typical process within a dust-free spraying environment includes:

  1. Loading Area
  2. Manual Dust Removal
  3. Electrostatic Dust Removal
  4. Manual/Automatic Spraying
  5. Drying Area
  6. UV Paint Curing Area
  7. Cooling Area
  8. Quality Inspection Area
  9. Receiving Area

3. Cleanrooms in Food Packaging

Cleanrooms dedicated to food packaging must adhere to strict standards to ensure optimal performance. Key requirements include:

  1. Adequate Air Supply: The cleanroom’s air supply should sufficiently dilute or eliminate indoor pollution.
  2. Correct Airflow Direction: Air should flow from cleaner areas to less clean areas, minimizing the movement of contaminated air. Proper airflow direction at doorways and other openings is crucial.
  3. Minimal Impact on Pollution: The air supply should not significantly increase indoor pollution.
  4. Controlled Indoor Airflow: Ensuring there are no high-concentration areas of pollutants within the cleanroom.

Meeting these guidelines allows for the measurement of particle or microbial concentrations to confirm compliance with cleanroom standards.

4. Cleanroom Testing for Food Packaging

Testing within a cleanroom catering to food packaging involves several critical assessments:

  1. Air Supply and Exhaust Volume: Measurement of air supply and exhaust volume, essential for turbulent cleanrooms. For one-way flow cleanrooms, air velocity measurements are imperative.
  2. Area-to-Area Airflow Control: Ensuring proper airflow direction between areas and validating pressure differences and airflow direction at doorways and within the room.
  3. Filter Leak Detection: Regular inspection of high-efficiency filters and their outer frames to prevent suspended pollutants from passing through.
  4. Isolation and Leak Detection: Verifying that suspended pollutants are effectively isolated from the cleanroom environment.
  5. Indoor Airflow Control: Conducting tests based on the airflow pattern, either turbulent or unidirectional, to ensure adequate airflow throughout the cleanroom.
  6. Particle and Microbial Concentrations: Finally, measuring particle and microbial concentrations, if necessary, to verify compliance with cleanroom design specifications.

5. Cleanrooms in Pharmaceutical Packaging

Cleanrooms used for drug packaging demand stringent environmental control. Requirements encompass:

  1. Air Purification: Providing the necessary level of air purification required for drug production, including regular testing of particle and microbial concentrations.
  2. Temperature and Humidity Control: Maintaining temperature and relative humidity compatible with production system requirements.
  3. Specialized Air-Conditioning: Designating specific air-conditioning systems for areas producing penicillin, high allergenic drugs, or anti-tumor drugs, with purified air exhaust.
  4. Dust Control: Installing effective dust-catching devices in areas prone to dust generation to prevent cross-contamination.
  5. 보관 조건: Ensuring that auxiliary production rooms, including storage areas, have ventilation facilities and temperature and humidity settings compatible with pharmaceutical production and packaging requirements.

6. Cleanroom Parameters and Air Changes

Cleanroom parameters play a crucial role in maintaining an optimal environment:

  • Purification Levels and Air Changes: Cleanrooms are classified into four levels based on air cleanliness: 100, 10,000, 100,000, and 300,000. Air change rates vary but typically range from 15 to 400 times per hour, depending on the cleanliness level.
  • Temperature and Relative Humidity: Temperature and humidity settings are tailored to the pharmaceutical production process and vary based on product type.
  • Cleanroom Pressure: Maintaining positive indoor pressure is essential to prevent external contamination. For certain cleanrooms, relative negative pressure is maintained to prevent contamination between areas.

Incorporating these stringent practices ensures that cleanrooms in the printing, packaging, food, and pharmaceutical industries meet the highest standards of cleanliness and compliance.


Q&A 섹션

1. Why are cleanrooms important in the printing and packaging industry?
Cleanrooms play a vital role in controlling temperature, humidity, and airborne particles, directly impacting product quality and pass rates.

2. What are the key aspects of cleanrooms in food packaging?
Cleanrooms for food packaging must ensure sufficient air supply, correct airflow direction, minimal indoor pollution, and controlled indoor airflow.

3. What types of tests are conducted in cleanrooms for food packaging?
Tests include air supply and exhaust volume measurement, area-to-area airflow control verification, filter leak detection, isolation and leak detection, indoor airflow control checks, and particle and microbial concentration measurements.

4. What are the critical requirements for cleanrooms in pharmaceutical packaging?
Pharmaceutical cleanrooms must provide air purification, control temperature and humidity, employ specialized air-conditioning for certain drugs, ensure effective dust control, and maintain suitable conditions in storage areas.

5. How are cleanroom parameters and air changes determined?
Cleanroom parameters, including air cleanliness, temperature, relative humidity, and pressure, are tailored to cleanliness levels and specific product requirements. Air changes per hour depend on the cleanliness level and can range from 15 to 400.


For more information on cleanroom technologies and their applications in various industries, visit our website at youthfilter.com.

Note: Cleanrooms are essential for maintaining product quality and safety. Always adhere to industry standards and guidelines when designing and operating cleanroom facilities.

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