Clean Air Systems
No. 4, Senthil Nagar, 100 Feet Road
Chennai - 600 094, Tamil Nadu, India
Phone: +(91)-(44)-23621476, 23622772
Mobile: 0091 9841074504, 0091 9551119111
Email: ravi@cleanairindia.com
Laminar Airflow
Bio-Hazard Safety Cabinet
Air Shower Entry System
Clean Room Pass Box
Powder Containment Booths
Sterile Garment Cabinet
Softwall Clean Room
Modular Clean Room
Positive Pressure Module
Clean Air Fan Filter Units
Laboratory Fume Exhaust Hoods
Laboratory Furniture
Air Curtains
Industrial Pollution control Equipment
Clean Room Validation
Metal Dorrs
 
1. How can a Cleanroom be defined?
2. What are various uses of Cleanroom?
3. Where are all the tiny particle and micro pollutants generated?
4. What is the size a micron?
6. What are the particle sizes of Contaminants in Microns?
7. How are Cleanrooms classified?
8. How do cleanrooms ensure cleanliness and better hygiene?
9. How small a particle does the human eye see?
10. Besides people, what are the other contaminants in a Cleanroom?
11. What is the Scope of the various currently available standards as per ISO standards?
7. What Precautions should be taken inside the cleanroom?
12. How does Laminar Air Flow Work?
13. What is the basic principle of Biosafety Cabinets?
14. How effective are the Air Shower Entry System in the Contamination Control Process?
15. What is Air Tunnel Technology?
16. How is Air Changes per hour is calculated in Cleanrooms?
17. What are the recommended garments for Aseptic Cleanrooms as per IEST RP CC-003.2 Standards?
18. What are the Personal Protection measures one should take while working in laboratories?
19. What are ISO 14644 Standards?
20. What are the equipments that must not be used inside a laboratory?
21. What are the key measures that must be taken while managing Waste Disposal in a laboratory?
22. What is laminar flow?
23. What does HEPA filter stand for?
24. What does ULPA filter stand for?
25. What exactly is an Airshower?
26.What is a pass-through Box or Pass box?
27. What is the size of a micron?
28. What elements comprise a Basis of CLEANROOM Design?
29. Define the general standards that have been adopted for laboratory fume hood exhaust?
30. What should the height of a stack be to shun re-entrainment?
31. How much should be the limit of material in a fume hood?
32. What should be the ideal Hood Face Velocity to capture exhaust fumes?
33. What are the different materials that are used in the design and development of Fume exhaust Hoods?
34. What are the Seven basic hood designs that Clean Air Systems deals in
35. What is the usage of HEPA Filter in Sterile Garment Cabinet?
36. What are the major areas where Softwall Clean are used and its advantages?
37. What are the salient features of Modular Clean Room that make them desirable and best option in their category?
How can a Cleanroom be defined?
Cleanroom is described as "a individually constructed room where the supply and distribution of air, presence of dust and airborne particle, room temperature, pressure and humidity are environmentally controlled to meet appropriate cleanliness." In more precise terms, a cleanroom has a controlled level of contamination that is specified by the number of particles per cubic meter at a specified particle size. To give perspective, the air outside in a general urban environment contains 33,000,000 particles per cubic meter, 0.5 μm and larger in diameter, corresponding to an ISO 9 cleanroom. Cleanrooms can vary in their sizes and are extensively used in biotechnology, life sciences, research and development, laboratories and other areas that are sensitive to environmental contamination.

What are various uses of Cleanroom?
Cleanrooms are commonly used in high technological industries such as electronics, semiconductor manufacturing, optical and biological industries where the production quality is extremely sensitive to the presence of airborne particles or dust. Commonly used air filters such as HVAC system are inefficient in collecting these particles and other factors also need to be taken into account to control the temperature, pressure, humidity and others factors to make the room suitable for production. Computer hard disk, microprocessor, semiconductors, medicine and pharmaceuticals, food processing, life-sciences research and development are some of the key areas where there is a need to control the micro-organism presence to maintain the quality and this is where cleanrooms find their usage.

Where are all the tiny particle and micro pollutants generated?
Human body is one of the biggest sources of particles generation, the quantity generally differs depending upon the person, children, their movement, kind of garment and other factors. For example, human body generates 100,000 particles per minute when sitting of standing without movement while walking quickly will generate 10,000,000 particles per minute. With such hig volumes of particles generated every minute there is a clear need to control these micro pollutants to maintain hygiene. Cleanrooms are an effective way of controlling these micro pollutants.

What is the size a micron?
A micron, which is also the short form for micrometer, is a unit of measurement equal to one millionth of a meter. A micron is actually 0.000039 of an inch.

What are the particle sizes of Contaminants in Microns?


How are Cleanrooms classified?
Cleanrooms are classified according to the number and size of particles permitted per volume of air. Large numbers like "class 100" or "class 1000" refer to FED-STD-209E, and denote the number of particles of size 0.5 µm or larger permitted per cubic foot of air. The standard also allows interpolation, so it is possible to describe e.g. "class 2000". Small numbers refer to ISO 14644-1 standards, which specify the decimal logarithm of the number of particles 0.1 µm or larger permitted per cubic meter of air. So, for example, an ISO class 5 cleanroom has at most 105 = 100,000 particles per m³. Both FS 209E and ISO 14644-1 assume log-log relationships between particle size and particle concentration. For that reason, there is no such thing as zero particle concentration. The table locations without entries are non-applicable combinations of particle sizes and cleanliness classes, and should not be read as zero. Because 1 m³ is approximately 35 ft³, the two standards are mostly equivalent when measuring 0.5 µm particles, although the testing standards differ. Ordinary room air is approximately class 1,000,000 or ISO 9.

US FED STD 209E Cleanroom Standards
Class maximum particles / ft³ ISO
equivalent
≥0.1 µm ≥0.2 µm ≥0.3 µm ≥0.5 µm ≥5 µm
1 35 7 3 1 ISO 3
10 350 75 30 10   ISO 4
100   750 300 100   ISO 5
1,000       1,000 7 ISO 6
10,000       10,000 70 ISO 7
100,000       100,000 700 ISO 8
 
ISO 14644-1 cleanroom standards
Class1 maximum particles / m ³ FED STD 209E
equivalent
≥0.1 µm ≥0.2 µm ≥0.3 µm ≥0.5 µm ≥1 µm ≥5 µm
ISO 1 10 2          
ISO 2 100 24 10 4      
ISO 3 1,000 237 102 35 8   Class 1
ISO 4 10,000 2,370 1,020 352 83   Class 10
ISO 5 100,000 23,700 10,200 3,520 832 29 Class 100
ISO 6 1,000,000 237,000 102,000 35,200 8,320 293 Class 1000
ISO 7       352,000 83,200 2,930 Class 10,000
ISO 8       3,520,000 832,000 29,300 Class 100,000
ISO 9       35,200,000 8,320,000 293,000 Room air
How do cleanrooms ensure cleanliness and better hygiene?
In several ways. Cleanroom technicians wear special clothing that's designed not to shed or let particles escape. Often before entering the cleanroom, personnel will walk through an airshower which blows off any particles using high velocity air. And, in the cleanroom, places where dust could settle like ledges and moldings are minimized. We also create an airflow pattern called laminar flow that constantly cleans the air by directing and re-circulating it through special filters.

How small a particle does the human eye see?
The naked eye can see particles as small as 40-150 microns.

Besides people, what are the other contaminants in a Cleanroom?
The other contaminants in a cleanroom besides people are:
  • Raw Materials
  • Chemical and Gases
  • Machinery and Equipment
What is the Scope of the various currently available standards as per ISO standards?
Standard Name Description
Class 1:         Classification of air cleanliness This standard covers the classification of air cleanliness in cleanrooms and associated controlled environments.
ISO 14644-2 Specification for testing and monitoring to prove continued compliance This part of the overall standard specifies requirements for periodic testing of cleanrooms and associated controlled environments to prove their continued compliance with ISO14644-1, and for the designated class of environmental cleanliness
ISO 14644-3 Metrology and test methods
This standard specifies the various methods and techniques which can be used to characterize and monitor various parameters in cleanrooms and other controlled environments.
ISO 14644-4 Design, Construction, and start-up  
ISO 14644-5 Cleanroom operations
This international standard specifies the basic requirements for operating cleanrooms and other controlled environments. It is primarily intended for those who are planning to carry out work in a cleanroom or any other controlled environment.
ISO 14698-1 General principles
This standard describes the principles and basic methodology for a formal system to assess and control bio-contamination where cleanroom technology is applied.
ISO 14698-2 Evaluation and interpretation of bio-contamination data:
This part of the standard concerning cleanroom technology and bio-contamination control describes basic principles and methodological requirements for all microbiological data evaluation.
ISO 14698-3 Methodology for measuring the efficiency: This standard concerns the efficiency of various processes that incorporated one or more of the following actions: rinsing, cleaning, disinfection, combined cleaning and disinfection by either biochemical or mechanical means. Methods of measuring the efficiency of the processes of rinsing and/ or cleaning and /or disinfection and/or combined cleaning and disinfection of wet soiled surfaces on which microorganisms may be present either with or without the formation of a bio-film, is explained in relation to the application of cleanroom technology.
What Precautions should be taken inside the cleanroom?
  • All personnel / visitors must wear Clean Room garments while entering Clean room
  • Clean Room Garments are to be stored properly in a laminar air flow storage cabinet
    • Personnel should not carry any personnel items such as pencils, pens, hand kerchiefs etc. into the Clean Room
  • Persons with skin ailments or coughing etc should not be allowed
  • Avoid talking inside the Cleanroom
    • For cleaning the Cleanroom it is always better to use liquid detergents and the cleaning process should be slow and the cleaning personnel should also wear Cleanroom garments
    • Do not use any blowing equipment inside or nearby a Cleanroom, instead, it is always recommended to use a vacuuming equipment for cleaning
    • Movement of materials from and to the Cleanroom must be as minimum as possible
    • Avoid touching by hand the material inside the Cleanroom, instead use forceps wherever possible
    • A sitting person sheds over 100000 particles, a moving person emits over one million particles and walking person emits 5 million particles of 0.5 micron size
How does Laminar Air Flow Work?
Laminar Air flow works on the principle of circulating filtered air in parallel-flowing planes in hospitals or other health care facilities. The system diminishes the risk of airborne contamination and exposure to chemical pollutants in surgical theaters, food preparation areas, hospital pharmacies, and laboratories. Constructed from all white seamless polypropylene, Clean Air System’s laminar air clean benches are the supreme answer for Class 100 (ISO 5) applications. The equipment comes in three different types namely, Horizontal, Vertical and Ceiling Laminar Air Flows. Standard on all horizontal laminar airflow workbenches, the controller constantly monitors filter conditions, alerting the operator of insufficient airflow. A distinctive function for the CleanAir Systems laminar airflow workbench is examination of parts or the assembly of equipments that require a clean, particulate and pollution free environment. CleanAir Systems horizontal laminar flow bench provides a HEPA filtered airflow across the work area, and a particulate-free work surface. While CleanAir Systems tissue culture hood provides excellent product shield, it receives rigorous QC/QA testing for highest cabinet and filtration standards. CleanAir System carefully selects and tests each HEPA filter to insure the reliability of the system. Our HEPA filters are naturally larger and therefore last longer than those in most competitive products. Our supremely designed Laminar Air flow Systems are used in following areas:
  • Life Science Research
  • Medical Laboratories
  • IV admixture preparation
  • Drug Compounding
  • Plant Cell Culture
  • Tissue Culture (non-biological)
  • Media Preparation
  • Pharmaceutical procedures
  • Electronic assembly

What is the basic principle of Biosafety Cabinets?
At CleanAir Systems Chennai, all Biosafety cabinet designing and crafting processes are approved by our Biosafety officer. Biosafety cabinets are utilized to provide primary containment in the laboratory when the researcher is using significantly contagious and infectious materials. Clean Air specializes in designing three types of biological safety cabinets:

Class I:
The Class I biological safety cabinet is an open-front negative pressure cabinet The exhaust air from the cabinet is filtered by a high-efficiency particulate air (HEPA) filter. The Class I biosafety cabinet will provide personnel and environmental protection, but not product protection.

Class II:
lass II biological safety cabinets (BSCs) are vital pieces of laboratory equipment in many life science applications requiring contamination control. The Class II vertical laminar-flow biological cabinet is an open-front, ventilated cabinet. This cabinet provides a HEPA-filtered, recirculated mass airflow within the work space. The exhaust air from the cabinet is also filtered by HEPA filters. Thus, the Class II Biosafety cabinet will provide personnel, environment and product protection. While HEPA filters are effective for trapping particulates and infectious agents, these filters will not capture volatile chemicals or gases. Product protection is offered by unidirectional (commonly called "laminar") down flow air in the work chamber, generated by the cabinet blower pushing air through the supply HEPA filter. Personnel protection comes from the intake air pulled into the front access opening of the cabinet. Environmental protection is provided by HEPA filters in the exhaust air stream of the cabinet. The use of a Class II cabinet in the microbiological laboratory offers the additional capability and advantage of protecting materials contained within it from extraneous airborne contaminants. This capability is provided by the HEPA-filtered, re-circulated mass airflow within the workspace.

Class III:
The Class III cabinet is a totally enclosed ventilated cabinet of gas-tight construction. Operations within the Class III cabinet are conducted through attached rubber gloves. When in use, the Class III cabinet is maintained through negative air pressure of at least 0.5 inches water gauge. Supply air is drawn into the cabinet through HEPA filters. The cabinet exhaust air is filtered by two HEPA filters, installed in series, before discharge outside of the facility. The exhaust fan for the Class III cabinet is generally separate from the exhaust fans of the facility's ventilation system.

How effective are the Air Shower Entry System in the Contamination Control Process?
Air Showers have always been questioned for their role in contamination control process. We at M/s. Clean Air Systems, Chennai - India, believes that the effectiveness of Air Shower Entry System is directly proportional to its design and use. Our supremely built air shower systems are incorporated within the design of an engineered cleanroom "entry system". Our Air Shower Entry Systems show efficiency of 90% particle removal on particles 5-20 micron, 60-65% on loose lead oxides, and that the use of a two air shower particle removal system, one prior to the change room and one prior to the cleanroom is considerably more effective than one. Clean Air System's Air Showers serve to guard your cleanroom environment from redundant contamination. Our Air showers to a great extent improve your Cleanroom's performance by removing surface contamination from clothing and cleanroom garments. Gowning/changing room areas are the common platform between a polluted environment and a clean room environment. Unfortunately, the changing or gowning process itself releases contaminants from outside world that can settle onto the "clean" garments. Air showers blow off and remove much of this contamination preventing it from entering the clean space.

What is Air Tunnel Technology?
Air shower systems have long been criticized for is the time delay that is caused due to the shift changes and to get personnel through the shower and working. The delay, however, far overshadows the damage that many people entering a Cleanroom simultaneously could have on particle counts. Spread out breaks and shift hours have been used over time as part of cleanroom operating parameters to minimize square footage allotted to gown rooms. Tunnel Technology helps reduce these delays. In State of the art cleanroom design, multiple person air showers are being widely used to shower personnel while walking. When designing multiple person air showers, a minimum of four feet in length should be designed for each person targeted to utilize the shower, per cycle. In a walk through tunnel design, optimum length for effectiveness is 32 feet to achieve acceptable contamination removal. Dimensions less than the above stated criteria will reduce air shower effectiveness and should be evaluated for cost benefit.

How is Air Changes per hour is calculated in Cleanrooms?
Air Changes per hour= Average airflow velocity* x room area x 60 min/hr.

What are the recommended garments for Aseptic Cleanrooms as per IEST RP CC-003.2 Standards?

Following garments are recommended for Aseptic Cleanrooms as per IEST RP CC-003.2 Standards:

  • Coverall
  • Boot
  • Hair Cover
  • Facial Cover
  • Barrier Gloves
What are the Personal Protection measures one should take while working in laboratories?
Extra care and precaution must be taken while working in laboratories where one can come in contact with chemicals and reagents. Clean Air Systems recommends use of rubber aprons, asbestos gloves, safety glasses, full face shields and approval respirators to protect personnel from spills, burns, spattering chemicals, flying fragments, and irritating fumes. In addition, the laminated safety glass doors on chemical fume hoods protect personnel from mishaps in the hood.

What are ISO 14644 Standards?
ISO 14644 Standards were first formed from the US Federal Standard 209E Airborne Particulate Cleanliness Classes in Cleanrooms and Clean Zones. The need for a single standard for cleanroom classification and testing was long felt. After ANSI and IEST petitioned to ISO for new standards, the first document of ISO 14644 was published in 1999.

What are the equipments that must not be used inside a laboratory?
Food, beverages, cigarettes, pipes, and cigars should not be permitted in the chemical laboratory under any circumstances. Chemical glassware should never be used to hold food. Laboratory technicians must never pipette toxic, corrosive, or radioactive chemicals by mouth; instead they should always use a rubber bulb or syringe.

What are the key measures that must be taken while managing Waste Disposal in a laboratory?
We at M/s. Clean Air Systems, reiterates that disposal of hazardous waste materials requires special handling and attention: Place all broken glass in specially marked metal containers, never in wasted baskets or containers used for paper or rags. Waste baskets or containers used for paper or rags. Flush dilute acids and alkalis down the drain with large quantities of water. Never pour flammable liquids not miscible with water, compounds that give off toxic vapors, or corrosive materials down the drain, special disposal containers are needed for each of these wastes.

What is laminar flow?
It's when all of the air in a cleanroom is forced to move in the same direction and speed to a filter. One common example of laminar flow is when the air moves from the ceiling through the floor, is forced up through the walls to be filtered above the ceiling and then re-enters the room and continues the cycle.

What does HEPA filter stand for?
High Efficiency Particulate Air. These replaceable filters will catch almost 100% of particles as small as .3 microns.

What does ULPA filter stand for?
Ultra Low Penetration Air. These filters can remove almost 100% of particles as small as .1 micron from circulating air.

What exactly is an Airshower?
It's a hallway or room leading to the entrance of the cleanroom. Often there is an airshower between the dressing room or gowning area and the main entrance to the cleanroom. In the airshower, high velocity air blows off debris that could contaminate the cleanroom environment. Sometimes de-ionizers are used to remove static thereby increasing the effectiveness of removing hair and lint.

What is a pass-through Box or Pass box?
A pass-through (pass-thru) is a chamber that allows items to be moved between cleanrooms or between cleanroom and non-cleanroom areas. Less traffic in and out of the cleanroom means fewer chances for contaminants to enter. Pass-throughs can also be designed so that only one door will open at a time. This, in conjunction with higher air pressure inside the cleanroom, forces particles out when the inner door opens. Pass-box in one of the pass-through.

What is the size of a micron?
A micron is a millionth of a meter. Invisible to the naked eye, just for comparison, a human hair is about 100 microns thick.

What elements comprise a Basis of CLEANROOM Design?
  1. Process description and process flow diagrams
  2. cGMP floor plan and general equipment arrangement
  3. Sized major process equipment list with utilities requirements/consumption
  4. Sized process support services utilities list (e.g., WFI, etc.)
  5. Functionality flow diagrams (process, people, product, material, components, waste, directionality of air flows)
  6. HVAC zoning and room classifications, including MICROBIAL limits
  7. Budget quality cost screening estimate
  8. Scope of Work matrix (design/specify/furnish/install/inspect/test/balance/certify/guaranty/challenge/qualify -i.e. identify explicity WHO is responsible for every element of the HVAC, envelope, and process)
  9. Realistic project schedule from kick-off through validation
  10. A listing of the appropriate/applicable regulatory authorities and jurisdictional venues for which the facility will have to be validated.
Define the general standards that have been adopted for laboratory fume hood exhaust?
The primary standard relating to laboratory fume hood exhaust is ANSI Z9.5 (1992). The entire standard can be ordered from Clean Air Systems Chennai.

What should the height of a stack be to shun re-entrainment?
Stack height must be determined by the height, width and length of the building, the wind currents around the building created by surrounding buildings or terrain, and the chemical make-up of the fume hood exhaust also play a crucial role in determining the height of the stack.

How much should be the limit of material in a fume hood?
Absolute minimum of material necessary to conduct any procedure in the fume hood. This completely guarantees that the fume hood can effectively capture and exhaust chemical fumes generated in the fume hood. The overall idea is to not use a fume hood for chemical storage and remove excess equipment while it is being used.

What should be the ideal Hood Face Velocity to capture exhaust fumes?
The hood design and the amount of exhausted air determine the efficiency of the Fume Hood. A fume hood should be designed to exhaust air at rates ample for complete removal of all contaminants. Below is a description of hood face velocity and conditions under which these are ideal.

Capture Velocity
Condition Hood face velocity
Very low toxic level materials; noxious odors, nuisance dusts, fumes 80 FPM
General lab use. Corrosive materials, moderate toxicity level materials tracer quantities of radioisotopes. TLV of 10=1000 PPM 100 FPM
Higher toxic level materials. TLV less than 10 PPM 125 to 150 FPM
Pathogenic micro organisms, very high toxic materials. TLV less than 0.01 PPM Enclosed GLOVE BOX should be used
 
What are the different materials that are used in the design and development of Fume exhaust Hoods?
Fume Hoods are generally made up of wood, sheet metal, fibre glass, stainless steel, polyvinyl chloride and polypropylene. Generally, wood is considered to have poor chemical resistance, and poor light reflectivity that makes the interiors of the room darker. On the same lines, polyvinyl chloride and polypropylene are mostly preferred for their excellent chemical resistance, fire-retardant properties, and are well suited to acid digestion application.

What are the Seven basic hood designs that Clean Air Systems deals in :
  1. Conventional Hood
  2. Conventional Hood with Reduced Face Velocity
  3. Conventional Hood with Use Factor
  4. Internally Supplied Hood
  5. Externally Supplied Hood
  6. Perforated Ceiling Supply Hood
  7. Horizontal Sliding Sash Hood
What is the usage of HEPA Filter in Sterile Garment Cabinet?
Garment Storage Cabinets manufactured by Cleanair™ India provide the finest quality solution to meet garment storage needs while making a positive contribution to maintaining the cleanliness of your controlled cleanroom environment. These cabinets are equipped with a blower and a HEPA filter in a fully contained enclosure constructed of powder-coated steel sheets, which will not shed particles or contaminate the environment of cleanroom. These cabinets not only provide a solution for storing cleanroom garments in a visible and organized manner, but also at the same time they remove particulate contamination from garments as they are stored and removed.

What are the major areas where Softwall Clean are used and its advantages?
Softwall Clean Rooms are commonly used in the microelectronics and medical mold injection industry as well as many others, post operative patient care, pharmaceutical filling, food product filling line. Soft-wall Cleanrooms widely are preferred over any other method of Cleanroom designs because of its versatility, economic, easily movable, easily re-locatable, can be totally dismantled and re-assembled with a minimum skilled man-power

What are the salient features of Modular Clean Room that make them desirable and best option in their category?
Modular clean rooms from M/s. Clean Air Systems are most preferred in the industry because of its pre-engineered wall systems, complete sound and thermal proofing nature and are designed manufactured specifically for multiple applications within very limited time availability. Clean Air modular clean rooms provide the most cost-effective Cleanroom environment construction and easily expandable and these modular clean rooms can accommodate anything from an equipment enclosure to pharmaceutical applications, medical implants manufacturing semiconductors etc.
 
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