Cleanroom

This article is about the manufacturing or research environment. For the method used to avoid copyright infringement, seeClean room design.For the software project methodology, seeCleanroom software engineering.For the TV episode, seeThe Clean Room.

Cleanroom used for the production of microsystems. Theyellow(red-green) lighting is necessary forphotolithography,to prevent unwanted exposure ofphotoresistto light of shorter wavelengths.

Cleanroom from outside

Entrance to a cleanroom with no air shower

Cleanroom formicroelectronicsmanufacturing withfan filter unitsinstalled in the ceiling grid

Cleanroom cabin for precision measuring tools

Typical cleanroom head garment

Acleanroomorclean roomis an engineered space that maintains a very low concentration of airborneparticulates.It is well isolated, well controlled fromcontamination,and actively cleansed. Such rooms are commonly needed for scientific research and in industrial production for all nanoscale processes, such assemiconductormanufacturing. A cleanroom is designed to keep everything from dust to airborne organisms or vaporised particles away from it, and so from whatever material is being handled inside it.

A cleanroom can also prevent the escape of materials. This is often the primary aim in hazardousbiology,nuclear work,pharmaceuticsandvirology.

Cleanrooms typically come with a cleanliness level quantified by the number of particles per cubic meter at a predetermined molecule measure. The ambient outdoor air in a typical urban area contains 35,000,000 particles for each cubic meter in the size range 0.5 μm and bigger, equivalent to an ISO 9 certified cleanroom. By comparison, anISO 14644-1 level 1 certified cleanroom permits no particles in that size range, and just 12 particles for each cubic meter of 0.3 μm and smaller. Semiconductor facilities often get by with level 7 or 5, while level 1 facilities are exceedingly rare.

History

The modern cleanroom was invented by AmericanphysicistWillis Whitfield.As an employee of theSandia National Laboratories,Whitfield created the initial plans for the cleanroom in 1960.Prior to Whitfield's invention, earlier cleanrooms often had problems with particles and unpredictableairflows.Whitfield designed his cleanroom with a constant, highly filtered airflow to flush out impurities.Within a few years of its invention in the 1960s, Whitfield's modern cleanroom had generated more than US$50 billion in sales worldwide (approximately $483 billion today).

The majority of the integrated circuit manufacturing facilities inSilicon Valleywere made by three companies: MicroAire, PureAire, and Key Plastics. These competitors made laminar flow units, glove boxes, cleanrooms andair showers,along with the chemical tanks and benches used in the "wet process" building of integrated circuits. These three companies were the pioneers of the use ofTeflonfor airguns, chemical pumps, scrubbers, water guns, and other devices needed for theproduction of integrated circuits.William (Bill) C. McElroy Jr. worked as an engineering manager, drafting room supervisor, QA/QC, and designer for all three companies, and his designs added 45 original patents to the technology of the time. McElroy also wrote a four-page article for MicroContamination Journal, wet processing training manuals, and equipment manuals for wet processing and cleanrooms.

Overview

A cleanroom is a necessity in the manufacturing ofsemiconductorsandrechargeable batteries,thelife sciences,and any other field that is highly sensitive to environmental contamination.

Cleanrooms can range from the very small to the very large. On the one hand, a single-user laboratory can be built to cleanroom standards within several square meters, and on the other, entire manufacturing facilities can be contained within a cleanroom with factory floors covering thousands of square meters. Between the large and the small, there are also modular cleanrooms.They have been argued to lower costs of scaling the technology, and to be less susceptible to catastrophic failure.

With such a wide area of application, not every cleanroom is the same. For example, the rooms utilized in semiconductor manufacturing need not besterile(i.e., free of uncontrolled microbes),while the ones used in biotechnology usually must be. Vice versa,operating roomsneed not be absolutely pure of nanoscale inorganic salts, such asrust,while nanotechnology absolutely requires it. What then is common to all cleanrooms is strict control of airborneparticulates,possibly withsecondary decontaminationof air, surfaces, workers entering the room, implements, chemicals, and machinery.

Sometimes particulates exiting the compartment are also of concern, such as inresearchinto dangerousviruses,or whereradioactive materialsare being handled.

Basic construction

First, outside air entering a cleanroom isfilteredand cooled by several outdoorair handlersusing progressively finer filters to exclude dust.

Within, air is constantly recirculated through fan units containing high-efficiency particulate absorbing filters (HEPA), and/or ultra-low particulate air (ULPA) filters to remove internally generated contaminants. Special lighting fixtures, walls, equipment and other materials are used to minimize the generation of airborne particles. Plastic sheets can be used to restrict air turbulence if the cleanroom design is of the laminar airflow type.

Air temperature andhumiditylevels inside a cleanroom are tightly controlled, because they affect the efficiency and means of air filtration. If a particular room requires low enough humidity to makestatic electricitya concern, it too will be controlled by, e.g., introducing controlled amounts of charged ions into the air using acorona discharge.Static discharge is of particular concern in the electronics industry, where it can instantly destroy components and circuitry.

Equipment inside any cleanroom is designed to generate minimal air contamination. The selection of material for the construction of a cleanroom should not generate any particulates; hence,monolithic epoxyorpolyurethanefloor coating is preferred. Buffed stainless steel orpowder-coated mild steel sandwich partition panelsand ceiling panel are used instead of iron alloys prone to rusting and thenflaking.Corners like the wall to wall, wall to floor, wall to ceiling are avoided by providingcoved surface,and all joints need to be sealed withepoxy sealantto avoid any deposition or generation of particles at the joints, by vibration andfriction.Many cleanrooms have a "tunnel" design in which there are spaces called "service chases" that serve as air plenums carrying the air from the bottom of the room to the top so that it can be recirculated and filtered at the top of the cleanroom.

Airflow principles

Airflow pattern for "Turbulent Cleanroom"

Airflow pattern for "Laminar FlowCleanroom "

Cleanrooms maintain particulate-free air through the use of eitherHEPAorULPAfilters employing laminar or turbulent airflow principles. Laminar, or unidirectional, airflow systems direct filtered air downward or in horizontal direction in a constant stream towards filters located on walls near the cleanroom floor or through raised perforated floor panels to be recirculated. Laminar airflow systems are typically employed across 80% of a cleanroom ceiling to maintain constant air processing. Stainless steel or othernon shedding materialsare used to construct laminar airflow filters and hoods to prevent excess particles entering the air. Turbulent, or non-unidirectional, airflow uses both laminar airflow hoods and nonspecific velocity filters to keep air in a cleanroom in constant motion, although not all in the same direction. The rough air seeks to trap particles that may be in the air and drive them towards the floor, where they enter filters and leave the cleanroom environment. US FDA and EU have laid down stringent guidelines and limits to ensure freedom from microbial contamination in pharmaceutical products.Plenumsbetweenair handlersandfan filter units,along withsticky mats,may also be used.

In addition to air filters, cleanrooms can also useultraviolet lighttodisinfectthe air.UV devices can be fitted into ceiling light fixtures and irradiate air, killing potentiallyinfectious particulates,including 99.99 percent of airborne microbial and fungal contaminants.UV light has previously been used to clean surface contaminants in sterile environments such as hospital operating rooms. Their use in other cleanrooms may increase as equipment becomes more affordable. Potential advantages ofUV-based decontaminationincludes a reduced reliance onchemical disinfectantsand the extension of HVAC filter life.

Cleanrooms of different kinds

Some cleanrooms are kept at apositive pressureso if any leaks occur, air leaks out of the chamber instead of unfiltered air coming in. This is most typically the case in semiconductor manufacturing, where even minute amounts of particulates leaking in could contaminate the whole process, while anything leaking outwould not be harmful to the surrounding community.The opposite is done, e.g., in the case of high-level bio-laboratories that handle dangerous bacteria or viruses; those are always held atnegative pressure,with the exhaust being passed through high-efficiency filters, and further sterilizing procedures. Both are still cleanrooms because the particulate level inside is maintained within very low limits.

Some cleanroomHVACsystems control thehumidityto such low levels that extra equipment likeair ionizersare required to preventelectrostatic dischargeproblems. This is a particular concern within the semiconductor business, because static discharge can easily damage modern circuit designs. On the other hand, active ions in the air can harm exposed components as well. Because of this, most workers in high electronics and semiconductor facilities have to wearconductive bootswhile working. Low-level cleanrooms may only require special shoes, with completely smooth soles that do not track in dust or dirt. However, for safety reasons, shoe soles must not create slipping hazards. Access to a cleanroom is usually restricted to those wearing acleanroom suit,including the necessary machinery.

In cleanrooms in which the standards of air contamination are less rigorous, the entrance to the cleanroom may not have an air shower. Ananteroom(known as a "gray room" ) is used to put on cleanroom clothing. This practice is common in many nuclear power plants, which operate as low-grade inverse pressure cleanrooms, as a whole.

Recirculating vs. one pass cleanrooms

Recirculating cleanroomsreturn air to the negative pressure plenum via low wall air returns. The air then is pulled by HEPA fan filter units back into the cleanroom. The air is constantly recirculating and by continuously passing through HEPA filtration removing particles from the air each time. Another advantage of this design is that air conditioning can be incorporated.

One pass cleanroomsdraw air from outside and pass it through HEPA fan filter units into the cleanroom. The air then leaves through exhaust grills. The advantage of this approach is the lower cost. The disadvantages are comparatively shorter HEPA fan filter life, worse particle counts than a recirculating cleanroom, and that it cannot accommodate air conditioning.

Operating procedure

In order to minimize the carrying of particulate by a person moving into the cleanroom, staff enter and leave throughairlocks(sometimes including anair showerstage) and wear protective clothing such ashoods,face masks, gloves, boots, andcoveralls.

Common materials such aspaper,pencils,andfabricsmade fromnatural fibersare often excluded because they shed particulates in use.

Particle levels are usually tested using aparticle counterand microorganisms detected and counted throughenvironmental monitoring methods.Polymertools used in cleanrooms must be carefully determined to bechemically compatiblewith cleanroom processing fluidsas well as ensured to generate a low level of particle generation.

When cleaning, only specialmopsandbucketsare used. Cleaning chemicals used tend to involve sticky elements to trap dust, and may need a second step withlight molecular weight solventsto clear. Cleanroom furniture is designed to produce a minimum of particles and is easy to clean.

A cleanroom is as much a process and a meticulous culture to maintain, as it is a space as such.

Personnel contamination of cleanrooms

The greatest threat to cleanroom contamination comes from the users themselves.In the healthcare and pharmaceutical sectors, control of microorganisms is important, especially microorganisms likely to be deposited into the air stream fromskin shedding.Studying cleanroommicroflorais of importance for microbiologists and quality control personnel to assess changes in trends. Shifts in the types of microflora may indicate deviations from the "norm" such asresistant strainsor problems with cleaning practices.

In assessing cleanroom microorganisms, the typical flora are primarily those associated with human skin (Gram-positive cocci), although microorganisms from other sources such as the environment (Gram-positive rods) and water (Gram-negative rods) are also detected, although in lower number. Common bacterial genera includeMicrococcus,Staphylococcus,Corynebacterium,andBacillus,and fungal genera includeAspergillusandPenicillium.

Cleanroom classification and standardization

The cleanroom processing bay of theKSCSpace Station Processing Facility.NASA maintains a standard of 100,000 class in the SSPF.

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 toFED-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; for exampleSNOLABis maintained as a class 2000 cleanroom.

A discrete, light-scattering airborne particle counter is used to determine the concentration of airborne particles, equal to and larger than the specified sizes, at designated sampling locations.

Small numbers refer toISO 14644-1standards, which specify the decimallogarithmof the number of particles 0.1 μm or larger permitted per m³of air. So, for example, an ISO class 5 cleanroom has at most 10⁵particles/m³.

Both FS 209E and ISO 14644-1 assume log-log relationships between particle size and particle concentration. For that reason, zero particle concentration does not exist. Some classes do not require testing some particle sizes, because the concentration is too low or too high to be practical to test for, but such blanks should not be read as zero.

Because 1 m³is about 35 ft³,the two standards are mostly equivalent when measuring 0.5 μm particles, although the testing standards differ. Ordinary room air is around class 1,000,000 or ISO 9.

ISO 14644-1 and ISO 14698

ISO 14644-1andISO 14698arenon-governmentalstandards developed by theInternational Organization for Standardization(ISO).The former applies to cleanrooms in general (see table below), the latter to cleanrooms wherebiocontaminationmay be an issue. Since the strictest standards have been achieved only for space applications, it is sometimes difficult to know whether they were achieved in vacuum or standard conditions.

ISO 14644-1defines the maximum concentration of particles per class and per particle size with the following formula

${\text{C}}_{\text{N}}=10^{\text{N}}\left({\frac {0.1}{\text{D}}}\right)^{2.08}$

Where${\text{C}}_{\text{N}}$is the maximum concentration of particles in a volume of 1m$^{3}$of airborne particles that are equal to, or larger, than the considered particle size which is rounded to the nearest whole number, using no more than three significant figures,${\text{N}}$is the ISO class number,${\text{D}}$is the size of the particle in$\mu$m and 0.1 is a constant expressed in$\mu$m. The result for standard particle sizes is expressed in the following table.

Class	Maximum particles/m3 a						FED STD 209E equivalent
	≥0.1 μm	≥0.2 μm	≥0.3 μm	≥0.5 μm	≥1 μm	≥5 μm
ISO 1	10b	d	d	d	d	e
ISO 2	100	24b	10b	d	d	e
ISO 3	1,000	237	102	35b	d	e	Class 1
ISO 4	10,000	2,370	1,020	352	83b	e	Class 10
ISO 5	100,000	23,700	10,200	3,520	832	d,e,f	Class 100
ISO 6	1,000,000	237,000	102,000	35,200	8,320	293	Class 1,000
ISO 7	c	c	c	352,000	83,200	2,930	Class 10,000
ISO 8	c	c	c	3,520,000	832,000	29,300	Class 100,000
ISO 9	c	c	c	35,200,000	8,320,000	293,000	Room air
aAll concentrations in the table are cumulative, e.g. for ISO Class 5, the 10 200 particles shown at 0,3 μm include all particles equal to and greater than this size. bThese concentrations will lead to large air sample volumes for classification. Sequential sampling procedure may be applied; see Annex D. cConcentration limits are not applicable in this region of the table due to very high particle concentration. dSampling and statistical limitations for particles in low concentrations make classification inappropriate. eSample collection limitations for both particles in low concentrations and sizes greater than 1 μm make classification at this particle size inappropriate due to potential particle losses in the sampling system. fIn order to specify this particle size in association with ISO Class 5, the macroparticle descriptor M may be adapted and used in conjunction with at least one other particle size. (See C.7.)

US FED STD 209E

USFED-STD-209Ewas aUnited Statesfederalstandard. It was officially cancelled by theGeneral Services Administrationon November 29, 2001,but is still widely used.

Class	Maximum particles/ft3					ISO equivalent
	≥0.1 μm	≥0.2 μm	≥0.3 μm	≥0.5 μm	≥5 μm
1	35	7.5	3	1	0.007	ISO 3
10	350	75	30	10	0.07	ISO 4
100	3,500	750	300	100	0.7	ISO 5
1,000	35,000	7,500	3000	1,000	7	ISO 6
10,000	350,000	75,000	30,000	10,000	70	ISO 7
100,000	3.5×106	750,000	300,000	100,000	830	ISO 8

Current regulating bodies include ISO, USP 800, US FED STD 209E (previous standard, still used).

• Drug Quality and Security Act (DQSA) created in Nov. 2013 in response to drug compounding deaths and serious adverse events.
• The Federal Food, Drug, and Cosmetic Act (FD&C Act) created specific guidelines and policies for human compounding.
  • 503A addresses compounding by state or federally licensed facility by licensed personnel (pharmacist/ physicians)
  • 503B pertaining to outsourcing facilities need direct supervision from a licensed pharmacist and do not need to be a licensed pharmacy. Facility is licensed through the Food and Drug Administration (FDA)

EU GMP classification

EU GMP guidelines are more stringent than others, requiring cleanrooms to meet particle counts at operation (during manufacturing process) and at rest (when manufacturing process is not carried out, but roomAHUis on).

Class	Maximum particles/m3
	At Rest		In Operation
	0.5 μm	5.0 μm	0.5 μm	5.0 μm
Grade A	3,520	20	3,520	20
Grade B	3,520	29	352,000	2,900
Grade C	352,000	2,900	3,520,000	29,000
Grade D	3,520,000	29,000	Not defined	Not defined

BS 5295

BS 5295 is aBritish Standard.

Class	Maximum particles/m3
	≥0.5 μm	≥1 μm	≥5 μm	≥10 μm	≥25 μm
Class 1	3,000		0	0	0
Class 2	300,000		2,000	30
Class 3		1,000,000	20,000	4,000	300
Class 4			200,000	40,000	4,000

BS 5295 Class 1 also requires that the greatest particle present in any sample can not exceed 5 μm.BS 5295 has been superseded, withdrawn since the year 2007 and replaced with "BS EN ISO 14644-6:2007".

USP <800> Standards

USP 800 is a United States standard developed by the United States Pharmacopeial Convention (USP) with an effective date of December 1, 2019.

Ramifications and further applications

Inhospitals,theatresare similar to cleanrooms for surgical patients' operations withincisionsto prevent any infections for the patient.

In another case, severelyimmunocompromisedpatients sometimes have to be held in prolonged isolation from their surroundings, for fear of infection. At the extreme, this necessitates a cleanroom environment. The same is the case for patients carrying airborne infectious diseases, only they are handled at negative, not positive pressure.

Inexobiologywhen we seek out contact with other planets, there is a biological hazard both ways: we must not contaminate any sample return missions from other stellar bodies with terrestrial microbes, and we must not contaminate possible other ecosystems existing in other planets. Thus, even by international law, any probes we send toouter spacemust be sterile, and so to be handled in cleanroom conditions.

Since larger cleanrooms are very sensitive controlled environments upon which multibillion-dollar industries depend, sometimes they are even fitted with numerousseismic base isolationsystems to prevent costly equipment malfunction.

See also

• Air ionizer
• Air conditioning
• Air quality index
• Contamination control
• Data recovery lab
• Indoor air quality
• Microfiltration
• Pressure room (disambiguation)
• Particle counter
• Pneumatic filter
• Secure environment
• Semiconductor device fabrication

External links

• Cleanroom Wiki--The Global Society For Contamination Control (GSFCC)