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ZJNF Cleanroom Laminar Flow Modular Clean Booth For Semiconductors Cosmetics Biomedicine Factory

Détails du produit

Lieu d'origine: Guangdong, Chine

Nom de marque: ZJNF

Numéro de modèle: Personnalisation

Conditions de paiement et d'expédition

Quantité de commande min: 1

Prix: negotiate

Détails d'emballage: paquet de contreplaqué/bois

Délai de livraison: 18 jours

Conditions de paiement: tt lc carte de crédit PayPal

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Les spécifications
Mettre en évidence:

cleanroom laminar flow booth

,

modular clean booth for semiconductors

,

cleanroom booth for biomedicine

Nom du produit:
403 Interdit
Code statut:
403
Serveur:
ouvertresty
Nom du produit:
403 Interdit
Code statut:
403
Serveur:
ouvertresty
Définition
ZJNF Cleanroom Laminar Flow Modular Clean Booth For Semiconductors Cosmetics Biomedicine Factory

Here is the English translation of the cleanroom booth introduction, incorporating the context from our previous discussion:


Cleanroom Booth Introduction

A cleanroom booth is a localized high-cleanliness environment device widely used in industries and scientific research that require strict control of dust, microorganisms, or chemical contamination. Below is a detailed explanation of its core applications, typical use cases, and safety requirements.


1. Primary Functions

Clean booths achieve air purification through high-efficiency filtration systems (e.g., FFU fan filter units), with key capabilities including:

  • Particle Control‌: Reducing airborne dust particles to ensure quality in precision manufacturing.
  • Microbial Isolation‌: Preventing bacterial contamination in pharmaceuticals, food, and other industries.
  • Environmental Stability‌: Maintaining constant temperature and humidity to avoid fluctuations affecting production.

2. Typical Applications

  1. Electronics & Semiconductor Industry

    • Used in chip and LCD panel production, requiring ISO Class 1-3 cleanliness (e.g., ≤1,000 particles ≥0.1μm per cubic meter).
    • Example: TSMC’s 5nm fabs use vertical laminar flow designs, achieving ISO Class 2 in critical zones.
  2. Pharmaceuticals & Biotechnology

    • Sterile drug production and cell culture must comply with GMP standards, with biosafety cleanrooms requiring positive pressure control.
    • Example: A pharmaceutical company reduced contamination risk to <0.01% with an ISO Class A aseptic filling line.
  3. Food & Precision Instruments

    • Prevents microbial contamination in food processing and avoids dust interference in precision instrument assembly.

3. Safety & Compliance Requirements

  1. Design & Construction Standards

    • Must comply with GB50073 Cleanroom Design Code, with contractors requiring relevant qualifications.
    • Hidden works require client approval, and system commissioning must involve certified technicians.
  2. Environmental Control

    • Airflow‌: Vertical laminar flow design with ≥500 air changes/hour.
    • Filtration‌: HEPA/ULPA filters with ≥99.9995% efficiency.
    • Pressure Gradient‌: 10–15 Pa between clean and non-clean zones.
  3. Materials & Equipment

    • Frame: Aluminum alloy or stainless steel; walls: anti-static coated steel panels (surface roughness Ra <0.13μm).
    • FFUs: Variable frequency control, noise ≤42 dB.
  4. Safety Measures

    • Equipped with VESDA smoke detection and gas suppression systems.
    • Biosafety booths require negative pressure to prevent contamination leakage
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