logo
Shenzhen Zhong Jian South Environment Co., Ltd.
Shenzhen Zhong Jian South Environment Co., Ltd.
Cases
Home /

China Shenzhen Zhong Jian South Environment Co., Ltd. Company Cases

Why choose us for your cleanroom project?

We are professional manufacturer providing one-stop air purification solutions for cleanroom.If you are considering a cleanroom project. Our team specializes in the design, engineering, and installation of cleanroom facilities tailored to stringent industry standards. Below, I will provide you with a clear overview of what a cleanroom is, why it matters, and how we propose to deliver a solution that fits your exact requirements. 1. What is a Cleanroom? A cleanroom is a controlled environment where airborne particles, temperature, humidity, and even pressure differential are precisely regulated. Unlike standard rooms, a cleanroom limits contamination through specialized airflow systems (HEPA or ULPA filtration), strict zoning, and carefully selected building materials that generate minimal dust or particulates. Think of it as “a bubble of certainty” in which your products, experiments, or processes are protected from invisible threats that could compromise quality. 2. Cleanroom Classifications Cleanrooms are classified by their level of cleanliness, defined by the number of particles per cubic meter of air. For example: ISO Class 5–7: Suited for semiconductor and pharmaceutical production. ISO Class 8: Common for medical device assembly, precision electronics, or biotech. We will align the cleanroom class with your specific industry needs, ensuring both compliance and operational efficiency. 3. Core Design Features Airflow & Filtration: HEPA/ULPA filter systems to achieve the desired particle counts. Material Choices: Non-shedding, anti-static wall panels, flooring, and ceilings. Environmental Controls: Temperature and humidity regulation for stable product quality. Pressure Cascades: Positive or negative pressure depending on whether the room is protecting the product (positive) or the outside environment (negative, e.g., in infectious disease labs). Modular Flexibility: Our systems are modular, allowing future expansions or reconfiguration with minimal downtime. 4. Project Execution Approach Consultation & Requirements Analysis: We’ll study your process, product, and compliance obligations. Concept Design & Engineering: Detailed 3D modeling of the cleanroom layout, airflow diagrams, and utilities. Fabrication & Installation: Precision assembly using factory-tested panels and equipment. Validation & Certification: Comprehensive qualification (IQ/OQ/PQ) to meet ISO, GMP, or FDA standards. Training & Handover: We provide hands-on training for operational staff to maintain cleanroom protocols. 5. Why Choose Us? Proven track record across pharmaceuticals, electronics, aerospace, and healthcare. Turnkey execution: from concept to commissioning. High-quality materials and engineering delivered on time and budget. Ongoing support and maintenance after project handover. Closing NoteYour process deserves a space where contamination is no longer a risk—it deserves a space engineered for perfection. With our expertise, we’ll transform your idea into a compliant, efficient, and future‑ready cleanroom environment. For more product details via ↓↓↓ Click Below ↓↓↓ HVAC Modular Clean Room Ceiling FFU Laminar Flow ISO Class 100 1000 10000 (iairpurifier.com) About us ↓↓↓ Click Below ↓↓↓ China Shenzhen Zhong Jian South Environment Co., Ltd. company profile (iairpurifier.com)

Top 5 Benefits of a Cleanroom Air Shower for Contamination Control

Introduction In industries such as pharmaceuticals, semiconductors, biotechnology, aerospace, and food processing, contamination control is critical. Even microscopic dust or bacteria carried on personnel or equipment can compromise production quality and threaten compliance with ISO and GMP cleanroom standards.One of the most effective solutions to this challenge is the cleanroom air shower. This specialized entry system uses high-velocity, HEPA-filtered air to remove contaminants before entry into a controlled environment. In this article, we’ll explore the top 5 benefits of cleanroom air showers and why every modern cleanroom facility should consider installing them. 1. Enhanced Contamination Control The primary function of a cleanroom air shower is to eliminate particles and dust that personnel or equipment may carry from outside environments.- How it works: As a person or cart passes through the chamber, nozzles blow high-speed jets of clean air (20–25 m/s) across surfaces.- Filtration system: The air passes through HEPA filters (≥99.99% efficiency at 0.3 microns), capturing even microscopic contaminants.- Result: Fewer airborne particles enter the cleanroom, ensuring a sterile and safe working environment.This benefit directly supports industries where product quality and sterility are non-negotiable. 2. Improved Product Quality and Safety Contamination doesn’t just affect cleanliness — it directly impacts product performance, reliability, and safety.- Pharmaceuticals: Contaminants can compromise drug safety and efficacy.- Semiconductors: Even a single dust particle can cause defects in microchips.- Biotechnology: Microbial contamination may ruin lab samples or experiments.By integrating air showers, manufacturers can ensure products are consistently high-quality, reducing risks of rejection, recalls, or regulatory issues. This not only safeguards consumers but also strengthens brand reputation. 3. Cost Savings on Cleanroom Maintenance Running a cleanroom can be expensive, especially with the frequent filter replacements, cleaning schedules, and energy costs required to maintain compliance.Cleanroom air showers help reduce these costs by:- Lowering the overall particle load inside cleanrooms.- Extending the lifespan of HEPA and ULPA filters in the cleanroom itself.- Reducing the need for frequent deep-cleaning procedures.Over time, this translates into significant cost savings, making the air shower not just a compliance tool but also a smart financial investment. 4. Compliance with International Standards Meeting global standards is a must in regulated industries. Air showers are designed to help facilities comply with:- ISO 14644 cleanroom classifications- GMP (Good Manufacturing Practice) guidelines- FDA cleanroom requirements for pharma and medical devicesHaving an air shower in place demonstrates a facility’s commitment to regulatory compliance and can ease the process of passing audits and inspections.For industries that regularly face inspections from regulatory agencies, installing an air shower is an essential risk-reduction measure. 5. Customizable and User-Friendly Design Modern air showers are designed to be both efficient and adaptable. Depending on the cleanroom requirements, systems can be customized with:- Different sizes: For single-person entry, multiple personnel, or equipment carts.- Door configurations: Automatic sliding or swing doors with interlocking systems.- Control features: Microprocessor-based systems with adjustable air velocity.- Durable materials: Stainless steel construction for long-term reliability.These features make the air shower easy to use, low-maintenance, and suitable for a wide range of applications. Conclusion – Why Every Cleanroom Needs an Air Shower In high-stakes industries, contamination is not just a nuisance — it’s a serious threat to safety, compliance, and profitability. Cleanroom air showers offer a simple, effective, and long-term solution by:- Enhancing contamination control- Protecting product quality and safety- Saving on maintenance costs- Supporting regulatory compliance- Offering flexible, user-friendly designsIf your facility requires strict environmental control, investing in a cleanroom air shower is a smart and necessary step.Ready to improve your cleanroom’s contamination control?Contact us today for expert guidance and a customized cleanroom air shower solution. ⇓⇓⇓ China Shenzhen Zhong Jian South Environment Co., Ltd. Contact Info (iairpurifier.com)

Unveiling the Cleanroom: The Core Fortress of Industrial Air Purification

In modern industrial production, many high-tech products and precision manufacturing processes demand extremely high levels of environmental cleanliness. Tiny dust particles, microorganisms, or even chemical molecules can lead to product defects, performance degradation, or even safety hazards. This is where the cleanroom comes in, becoming a critical facility for ensuring product quality and production efficiency. What is a Cleanroom? A cleanroom, as its name suggests, is an enclosed space where the concentration of airborne particulates is strictly controlled. It uses a series of precise air purification equipment and systems to limit dust, microorganisms, chemical pollutants, and other contaminants in the indoor air to specific standards. Its core objective is to provide a controlled, ultra-clean environment for production or experimentation. Cleanliness Classes: The "ID Card" of a Cleanroom The cleanliness level of a cleanroom isn't a one-size-fits-all standard; instead, it's divided into different cleanliness classes based on application requirements. The most common classification standard is the ISO 14644-1 international standard, which defines cleanliness based on the number of particles of different sizes (e.g., 0.1 micrometers, 0.5 micrometers, 5 micrometers, etc.) per cubic meter of air. The smaller the cleanliness class number, the higher the cleanliness level, and the more stringent the environmental control requirements. ISO Class 9: This is the lowest cleanliness class, similar to a typical indoor environment, but still requires airflow control. ISO Class 7/8: Commonly found in industries like food and beverage production, and general electronics assembly. ISO Class 5: A frequently used class in semiconductor manufacturing, precision instrumentation, and medical device production. At this level, there are no more than 3,520 particles of 0.5 micrometers and larger per cubic meter of air. ISO Class 3/4: Reserved for cutting-edge fields with extremely high cleanliness demands, such as chip manufacturing, biopharmaceutical production, and aerospace. Achieving these classes implies strict limits on even nanometer-sized particles. Choosing the appropriate cleanliness class is the first step in designing and building a cleanroom, as it directly determines subsequent equipment selection and operating costs. FFU Fan Filter Units: The Deliverers of Clean Air In a cleanroom system, the FFU (Fan Filter Unit) plays a vital role. It's a self-contained, modular terminal air supply unit with an integrated fan and filter, typically installed in the cleanroom's ceiling grid. Independence: Each FFU unit is self-powered and can operate independently, without relying on a central air conditioning system for air supply. This allows for greater flexibility in cleanroom layout. High-Efficiency Filtration: FFUs contain built-in high-efficiency filters (HEPA/ULPA), which can effectively capture over 99.95% (or even higher) of tiny airborne particles. Laminar Airflow: FFUs typically employ a downward laminar airflow pattern, delivering clean air uniformly into the work area while simultaneously pushing contaminants generated during production downwards towards the return air vents. This effectively prevents air short-circuiting and cross-contamination. Energy Efficiency: Modern FFUs mostly use DC (Direct Current) brushless motors. Compared to traditional AC (Alternating Current) motors, they offer higher energy efficiency and lower operating noise, significantly reducing running costs. Air Filters: The "Lungs" of the Cleanroom Air filters are the core components of cleanroom air purification; they act as the "lungs" of the cleanroom, responsible for capturing various airborne contaminants. Based on their filtration precision, air filters are typically categorized as: Pre-filters: Primarily used to filter large dust particles, hair, etc., protecting medium and high-efficiency filters and extending their lifespan. Medium-efficiency filters: Offer higher filtration efficiency than pre-filters and are used to remove smaller particles, often serving as pre-filters for high-efficiency filters. High-Efficiency Particulate Air (HEPA) filters: These are the heart of the cleanroom, capable of capturing over 99.95% of particles 0.3 micrometers and larger. Ultra-Low Penetration Air (ULPA) filters: Used in applications requiring extremely high cleanliness, with filtration efficiency for 0.12-micrometer particles exceeding 99.999%. Chemical filters (Molecular filters): Used to remove harmful gases and molecular contaminants from the air, such as acidic gases, alkaline gases, and VOCs, particularly crucial in semiconductor and biopharmaceutical industries. Other Key Air Purification Equipment Beyond FFUs and various filters, cleanrooms also rely on several other air purification devices working in synergy: Cleanroom Air Handling Units (AHU): Responsible for pre-treating fresh air entering the cleanroom, including controlling temperature, humidity, and differential pressure, as well as initial filtration. Air Showers: Located at the entrance/exit points for personnel into the cleanroom, they use high-velocity clean airflow to remove dust from personnel or material surfaces, preventing external contaminants from entering the cleanroom. Pass Boxes: Used for transferring materials into and out of the cleanroom, minimizing frequent personnel movement and reducing cross-contamination. HEPA Filter Boxes (High-Efficiency Air Outlets): Some cleanrooms may use supply air outlets with integrated HEPA filters instead of FFUs to achieve terminal filtration. Return Air Systems: Responsible for drawing air back from the cleanroom, which is then re-filtered and conditioned before being re-supplied, forming a circulating purification loop. Conclusion A cleanroom is a highly integrated and precise system engineering endeavor. Its cleanliness class, FFUs, air filters, and other auxiliary purification equipment collectively form a complete chain that ensures a clean environment. For industrial production, investing in a cleanroom isn't just about meeting standards; it's about improving product quality, reducing defect rates, ensuring stable production, and ultimately achieving sustainable development and core competitiveness for the enterprise.  Link: Modular ISO Clean Room , Dust Free H13 H14 Prefabricated Clean Room For Lab (ecer.com)

‌Testing Procedures for HEPA Glass Fiber Air Filters

‌Testing Procedures for High-Efficiency Glass Fiber Air Filters During Production‌ Testing during production involves three key stages: raw material inspection, process control, and finished product testing. Detailed procedures and methods are as follows: I. Raw Material Inspection ‌Filter Media Performance Testing‌ ‌Physical Properties‌: Measure paper thickness (accuracy: ±1μm) and basis weight (g/m²) to ensure permeability and strength compliance; analyze fiber diameter (typically 1–10μm) and distribution density via Scanning Electron Microscopy (SEM) ‌Chemical Stability‌: Conduct acid/alkali corrosion resistance tests (immersion in 30% H₂SO₄/NaOH for 48 hours), and evaluate thermal shrinkage (≤1%) and strength retention (≥80%) after high-temperature exposure (200°C for 24 hours) ‌Permeability Screening‌: Perform water repellency testing (spray test); premium-grade media must resist water penetration for 24 hours ‌Frame and Sealing Materials‌ Inspect dimensional tolerances of aluminum/stainless steel frames (e.g., side length deviation: ±2mm), flatness (≤6mm), and perpendicularity (deviation: ±3°) Verify integrity of sealant gasket joints to prevent air leakage II. In-Process Testing ‌Filter Core Fabrication Monitoring‌ Ensure uniform pleat spacing without damage; control core height tolerance (±1mm) and pleat count (e.g., 39–41 pleats) Regulate polyurethane AB adhesive ratio (A=1:2.5) during potting; adhesive penetration height ≤5mm to prevent media-frame separation ‌Structural Assembly Checks‌ Flatten and shape protective mesh to eliminate rust/deformation; ensure burr-free filter core edges and diagonal length deviation ≤3mm after mesh fixation For groove-type filters, fill with non-Newtonian sealant to ensure volatility resistance and acid/alkali tolerance III. Finished Product Testing ‌Integrity Leak Testing (Core Item)‌ ‌Scanning Method‌: Use aerosol photometers/particle counters with upstream PAO/DOP challenge aerosol (10–100μg/m³). Scan downstream at 3cm from the surface (5cm/s speed); leakage rate ≤0.01% qualifies ‌Critical Areas‌: Test for pinholes in media, media-frame adhesive joints, and gasket-support frame seams ‌Performance Parameter Testing‌ ‌Filtration Efficiency‌: Apply sodium flame method (NaCl aerosol) or particle counting (0.1–0.3μm particles); efficiency for 0.3μm particles must be ≥99.97% (H13/H14 grade) ‌Resistance & Airflow‌: Initial resistance ≤105% of nominal value at rated airflow; airflow deviation

Answers to Core Issues of FFU Fan Filter Unit products

"Why did semiconductor yield rates suddenly drop?" "Why do pharma cleanrooms keep failing GMP audits?" – These industrial pain points often trace back to air purification systems. Drawing from 15 years of cleanroom expertise and 800+ enterprise procurement cases, we reveal the truth behind selecting FFU (Fan Filter Units) with data-driven insights. ‌I. Industry-Specific Customization‌ 1. "How do FFUs prevent electrostatic damage to chips in electronics factories?" ‌Solution‌: Galvanized steel casing with grounding design + ion neutralizers (Case study: 23% reduction in ESD defects) ‌Key metric‌: Surface resistance ≤10⁶ Ω (Compliant with ANSI/ESD S20.20) 2. "Which certifications must FFUs meet for biopharmaceutical applications?" ‌Critical compliance‌: GMP Annex 1, ISO 14644-3, FDA 21 CFR Part 11 ‌Sterility assurance‌: Seamless welded housing + in-situ sterilization capability ‌II. Cost-Performance Tradeoffs‌ 3. "How often to replace HEPA filters? What’s the annual maintenance cost?" ‌Data comparison‌: Standard filters: 6-8 months (high-dust environments) Long-life filters: 12-18 months (nano-coated surface technology) ‌Interactive tool‌: Embedded TCO calculator 4. "How to reduce energy consumption in FFU clusters?" ‌Innovation‌: EC motor smart speed control (35-50% power savings) ‌Proof‌: $38K annual energy reduction at Tier-1 solar manufacturer ‌III. Procurement Decision Support‌ 5. "Which technical specs are mandatory for tender documents?" ‌Essential parameters‌: Airflow: 300-1500 m³/h Noise level: ≤52 dB(A) Filtration: H13/H14 class (EN 1822 certified) 6. "How to retrofit FFUs in legacy facilities?" ‌Service highlight‌: 3D scanning for non-standard dimensions (72-hour CAD drawing guarantee) ‌IV. Hidden Value Drivers‌ 7. "Why do top wafer fabs choose galvanized steel FFUs?" ‌Performance validation‌: Galvanized steel: 500+ hours salt spray resistance Stainless steel: 30% higher cost, similar acid resistance 8. "How to integrate FFUs with smart factory systems?" ‌IoT-ready‌: Modbus RTU protocol + cloud-based monitoring dashboards If you want to know more about the FFU,feel free to contact us. https://www.iairpurifier.com/videos-44431981-aluminum-alloy-fan-filter-unit-ffu-with-h13-h14-hepa-filter-ideal-air-flow-range-500-2000-m-h.html
1