Tag Archives: Clean Rooms

Stricter procedures, reporting, and new antimicrobial products play a role

By Frank Sylvester, Sylvester Solutions

For anyone who has ever been admitted to a hospital for an emergency, illness, or scheduled procedure, usually the last thing on their mind is exposure to another, potentially more devastating health problem-infection. Yet there is no denying that drug-resistant pathogens are a growing threat to all people, especially in health care settings.

The Centers for Disease Control and Prevention (CDC) reports that “each year nearly 2 million patients in the United States get an infection in a hospital. More than 70% of the bacteria that cause hospital-acquired infections [HAIs] are resistant to at least one of the drugs most commonly used to treat them. Persons infected with drug-resistant germs are more likely to have longer hospital stays and require treatment with second- or third-choice drugs that may be less effective, more toxic, and/or more expensive.”1

The Committee to Reduce Infection Deaths (RID) goes on to say that “infections contracted in hospitals are the fourth largest killer in America. Every year in this country, an estimated 103,000 patients die as a result of these infections, a startling statistic since it is larger than the combined deaths from AIDS, breast cancer, and auto accidents.”2 But the cost is not in lives lost alone. Says Betsy McCaughey, PhD, RID founder and chair, “Hospital infections affect 2 million Americans every year and add $30.5 billion to the nation’s health care tab.” For example, McCaughey points out that depending on the type of infection, the additional 1.9 million or so patients who contract a non-fatal infection will spend from one to 30 extra days in the hospital for treatment.

There’s no denying that, in hospitals throughout our nation, marvelous procedures save patients at the threshold of death every day, and the health care profession should be applauded for its successes. Unfortunately, there’s also the fact that as many as one out of every 20 patients contracts an infection-and therein lies the problem waiting for resolution.

The ‘Superbug’

One of the deadliest germs responsible for hospital infection and one of the hardest to treat is called methicillin-resistant Staphylococcus aureus (MRSA)-more commonly known as “staph.”

Infectioncontroltoday.com describes staph as “bacteria commonly carried in the nose and skin.”3 Around 25 percent of the population carry “colonized” staph in their noses, meaning they don’t suffer from any symptoms or complications. However, an injury to the skin can give the bacteria a chance to enter the body. Although most staph infections of the skin are minor, causing pimples or boils, and are treatable with antibiotics, more serious versions can lead to bloodstream, lung, or other infections.


Figure 1. Patient waiting areas, emergency rooms, and examination rooms are all environments for potential infections to lurk, with stools, gurneys, and wheelchairs as just some of the surfaces where staph and other germs can come in contact with patients. Photos courtesy of Sylvester Solutions.
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Generally, staph is most often spread via skin-to-skin contact and through open wounds. Indirect contact from infected towels, benches, gurneys, chairs, bedding, or clothing is another major source of bacterial transfer (see Fig. 1).

The legal position

Many people and organizations believe that health care institutions should be required to publicly report their infection rates, giving patients the ability to review infection control data and thereby providing them with a more educated and informed decision as to what facility to select. But, according to a New Hampshire Public Radio (NHPR) report, as of February 2007, only 15 states were mandating hospitals to report cases of infection by law. Furthermore, the infection rate data that is made available to the public by those hospitals mandated to supply them can be skewed.


Figure 2. Top: Seating surfaces are an ideal place for germs to live and multiply. Hospital waiting rooms with seating fixtures covered in fabric represent opportunities for pathogens to thrive. Bottom: Seats upholstered with CMI’s “Dimensions” line of antimicrobial materials actually kill microbes with embedded nanoscale silver. Photos courtesy of Sylvester Solutions.
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The State of Pennsylvania is one of the 15 that currently does mandate the reporting of infection data. In 1986, the Pennsylvania Health Care Cost Containment Council (PHC4) was established as an independent state agency by the General Assembly and Governor of the Commonwealth. As stipulated in its report “Hospital-acquired Infections in Pennsylvania,” “the main objective of PHC4 is to help improve the quality and restrain the cost of health care. PHC4 promotes health care competition through the collection, analysis, and public dissemination of uniform cost and quality-related information.”4

On the surface, this all sounds well and good, but the actual data being compiled and made public may not be. Says Alice McDonnell, MPA, RN, an infection control nurse since 1977, “Some of the data used by PHC4 is certainly skewed. The billing procedure codes do not differentiate between those [persons] who have acquired an infection while a patient in the hospitals vs. those who already had an infection when they arrived.”

For example, according to the current reporting procedures, if during the course of gall bladder surgery surgeons determined that the organ was infected (an infection acquired prior to being admitted to the hospital), this incident would be coded/billed as an HAI-when, in fact, it was not.

In fact, the CDC reports that 20 to 30 percent of patients admitted to hospitals may already carry infectious germs, bringing them into the facility rather than acquiring them while there.1 This data is supported by McDonnell’s experience. “We perform nasal swabs on every patient admitted to our ICUs to determine if the patient is infected with, or colonized with, methicillin-resistant Staphylococcus aureus. And since the inception of this program, the CDC statistics have held true: 20 to 30 percent of the patients tested have proven positive,” she says.

McDonnell notes that the turnaround time for the swab tests is quick, usually within two hours, and “once we know that a patient has a resistant organism, we can take appropriate precautions to prevent transmission to other patients or to our employees.”

Although infection control principles are absolute, McDonnell says staff sometimes have difficulty applying the principles to certain patients because each patient and condition is different. “I always tell the staff to think about three basic concepts: What disease or organism does the patient have; how is that disease transmitted to others; and what precautions do you need to take to prevent it from being transmitted?”

Dealing with HAIs

So what steps can hospitals take to combat the problem of HAIs? Well, McDonnell points out that “the easiest, most efficient, and cost-effective means of reducing HAIs is washing your hands.” And some hospitals have implemented a “no necktie” policy in an effort to further reduce the rate and mode of spreading germs.

But Kathy Bartkowski, an RN since 1969 and an infection control nurse for the past eight years, says that ultimately, “You need to determine policies, protocols, and strict procedures that must be followed by all hospital staff-from nurses to physicians right on down to house cleaning personnel.”

Still, though establishing standard hospital policies and procedures is certainly a major component in combating HAI, enforcing them effectively may present another issue. For example, although hospital administration, nurses, and other employees are required to follow infection control rules and protocols, physicians, who are independent practitioners, are not.

“Some physicians are very good at infection control procedures-e.g., washing hands, cleaning stethoscopes-while others simply are not,” says Bartkowski. “To expect a physician to wipe his/her stethoscope with an alcohol swab before and after seeing every patient just isn’t going to happen. It comes down to time and resources-in other words, cost.”

Antimicrobial materials

While the most common means of bacterial transmission remains the hands, it follows that if you can reduce the amount of bacteria present on surfaces to begin with, you’re less likely to pick it up and pass it along.

This is the thinking behind the introduction of new antimicrobial fabrics into the seating and bedding products used in health care environments including hospitals, clinics, dental offices, and nursing homes.

One such product is CMI Enterprises’ (Miami, FL) “Dimensions” fabric line, which incorporates the company’s Nanocide™ antimicrobial treatment. The treated fabric features embedded nanoscale silver particles, as opposed to a topical application that would wear off over time. Silver is a powerful, natural antibiotic. Acting as a catalyst, the silver disables the enzyme that one-celled bacteria, viruses, and fungi need for oxygen metabolism. As a result, the microbes suffocate (see Fig. 2).

The nanotechnology employed does not require the bacteria to ingest or absorb the biocide. It is killed when it comes into contact with the ion field on the surface. Test results for CMI’s “Dimensions” line have shown that 99.9% of resistant staphylococcus germs that come in contact with it are killed within 30 minutes (see Fig. 3).


Figure 3. A colony of Aspergillus niger (left) and the fungi Candida albicans (right) surround swatches of CMI’s “Dimensions” antimicrobial treated fabric. All fungi and germs are killed not only on the white treated vinyl but also beyond the blue ring. Photos courtesy of Sylvester Solutions.
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“The use of silver at the nanoscale is allowing manufacturers to innovatively add antimicrobial properties to an ever expanding range of products,” says Marlene Bourne, president and principal analyst of Bourne Research LLC (Scottsdale, AZ). “Even better, with this approach, there’s a greater assurance of longevity and performance. Since the germ-fighting properties won’t wear off in a short period of time, hospitals can confidently make the capital investment necessary for this kind of next-generation infection control.”

Antimicrobial fabrics represent one more important and effective tool for the health care community to bring to bear against the growing problem of hospital infection.


Frank Sylvester is president of Sylvester Solutions, a market and business development company. He graduated from Syracuse University in 1983 with a B.A. in business.

References

  1. The Centers for Disease Control and Prevention (CDC) web site; http://www. cdc.gov.
  2. The Committee to Reduce Infection Deaths (RID) web site; http://www.hospitalinfection.org.
  3. Infection Control Today web site; http://www.infectioncontroltoday.com.
  4. “Hospital-acquired Infections in Pennsylvania,” Pennsylvania Health Care Cost Containment Council (PHC4), 2006; http://www.phc4.org/reports/hai/05/docs/hai2005report.pdf.

Cleanroom Furniture


July 1, 2007

Comfort is important to contamination-control professionals confined to the cleanroom or lab for extended periods of time. Equally important, however, is ensuring that furniture conforms to cleanliness requirements, so as not to jeopardize the integrity of the controlled area. This month’s spotlight features a selection of furniture for critical environments that does just that.

Compiled by Carrie Meadows

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Ergonomic cleanroom seating
Chairs from BioFit Engineered Products are scientifically designed and independently tested to meet rigorous cleanroom standards. The chairs are designed with an eye on cleanroom space, tasks workers will be performing, and how the seating is expected to function in such a context. They provide ergonomic comfort to reduce work-related spinal conditions, such as unnatural bending of the spine caused by leaning over to perform delicate assembly work. The chairs come with a 13-year warranty to protect the buyer’s investment. BioFit offers Class 1, 10, 100, and 1,000 cleanroom chairs. To learn more, call (800) 597-0246 or visit BioFit online.

BioFit Engineered Products
Bowling Green, OH
www.biofit.com

Perforated stainless-steel tables

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Clean Air Products’ Series 64 perforated stainless-steel cleanroom tables allow uniform airflow through the work surface and eliminate eddies and stagnant air pockets that are on or above the work surface of solid-top tables. They feature a stainless-steel support frame and are ideal for vertical flow cleanroom applications. Series 64CT continuous-top and Series 64PF perimeter-frame models are available. Clean Air Products also provides custom modification services to create products and systems designed to satisfy specific application requirements. Call (800) 423-9728 or visit the company’s web site.

Clean Air Products
Minneapolis, MN
www.cleanairproducts.com

Antimicrobial-treated fabrics

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CMI Enterprises, a leading supplier of soft-trim textiles and fabrication solutions to the health care, contract furniture, and transportation industries, has announced its new environmentally friendly Nanocide™ Antimicrobial. The company’s newly released “Dimensions” line of coated fabrics for upholstery and bedding will be the first of its kind for the industry, featuring the Nanocide™ Antimicrobial. Test results for the “Dimensions” line have shown that 99.9% of resistant staphylococcus germs that come in contact with it are killed within 30 minutes. The nanotechnology and process developed by CMI permanently places or embeds the nanoparticles into the surface area of the product. When the recommended cleaning and care instructions are properly followed, the nanoparticles cannot be washed away, worn off, or depleted over time. To request samples, call (800) 346-0475 ext. 313 or e-mail [email protected].

CMI Enterprises
Miami, FL
www.nanocide-cmi.com

Distributor of cleanroom furniture

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Connecticut Clean Room Corporation (CCRC) offers a complete line of cleanroom furniture including a wide selection of custom stainless-steel furniture by Eagle, InterMetro, Advance Tabco, and BioFit. All of the products meet or exceed the stringent requirements needed in critical environments ranging from Class 100,000 to Class 10. With more than 25 years of experience in cleanroom products, the company can assist in selecting the right furniture for cleanroom applications. Look for the BEE SMART symbol to see which of the offerings can be converted or built to specifications. CCRC’s new catalog features an assortment of special products that meet all critical manufacturing, industrial, and sanitary standards. To receive a catalog or for information on BEE SMART, call (860) 589-0049 and ask the Customer Care Team for more details.

Connecticut Clean Room Corporation
Bristol, CT
www.ctcleanroom.com

Technical seating for industrial applications

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Gibo/Kodama Chairs are made in the U.S. and can be found in cleanroom production lines, biomedical/pharmaceutical labs, and office environments-anywhere ergonomics and productivity are vital. Technical seating products for ESD protection, cleanrooms, and harsh environments are used by top technology companies. For more information on Gibo/Kodama cleanroom furniture and task seating, please visit the distributor, RPA, at www.rpaproducts.com or call (951) 273-0620.

Gibo/Kodama Chairs
Huntington Beach, CA
www.gkchairs.com

Lab workstations with exhaust

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JST Manufacturing Inc. offers a full line of exhausted laboratory workstations for safe handling of acids, bases, or solvents. Materials of construction consist of corrosion-resistant 304L stainless steel, FM4910 approved acid-resistant plastic, or a combination of both. JST meets all regulatory requirements, and its exhausted units have been ASHRAE tested for safety. Desiccators, tables, pass-throughs, carts, fixtures, and smock, waste, and drum cabinets are also offered in addition to support tools for cleaning. Contact JST at (800) 872-0391 or visit the web site.

JST Manufacturing Inc.
Boise, ID
www.jstmfg.com

Vibration isolation workstation

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The Class 100 cleanroom-compatible (Class 10 compatibility optional) 2000 Series Variable Height Vibration Isolation Workstation from Kinetic Systems allows the user to raise or lower the tabletop with a simple switch to any height throughout a range of 24 to 36 inches. Additional height ranges are also available through consultation with the factory. The workstation features automatic leveling, delivers excellent vertical and horizontal isolation efficiencies, and has low natural frequencies, which makes it suitable for repetitive processes in which external vibrations adversely affect the operation of precision equipment. For more information, call (617) 522-8700.

Kinetic Systems Inc.
Boston, MA
www.kineticsystems.com

Range of submicron cleanroom furnishings

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NTA Industries designs and produces stainless-steel cleanroom furniture in the U.S. that are used in semiconductor, medical, biotech, pharmaceutical, aerospace, and precision molding industries worldwide. The furnishings provide sterility and reliability for high-tech companies. For more information on NTA Industries’ stainless-steel cleanroom furniture, please visit the distributor, RPA, at www.rpaproducts.com, or call (951) 273-0620.

NTA Industries
Belmont, MI
www.ntaindustries.com

Furniture for critical environments

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Palbam Class supplies high-quality cleanroom furniture, featuring designs that reduce particle/microbial accumulation; improve user/furniture interaction such as human factors, ergonomics, and wipe-down; create a modern high-tech environment that encourages adherence to cleanroom protocols; and create a positive impression on users and customers as to the standard of cleanroom activities. For more information, visit the company’s web site.

Palbam Class
Afula, Israel
www.palbamclass.com

Auto-adjusting workstation

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Terra Universal’s ErgoHeight™ auto-adjusting workstation positions the work surface at the correct height for each operator. Its high-torque, low-RPM motorized lifters safely handle a net load of 420 lb., adequate for most benchtop equipment. A frame-mounted control panel stores memory positions for up to four bench heights between 28 and 48 inches floor-to-top. The thermally protected lifters are sealed to the underside of the benchtop to eliminate particle generation, making this unit compatible with ISO 5 (Class 100, per U.S. Fed. Std. 209) cleanrooms. Specialized designs include vibration-isolated tops or perforated tops with down-draft exhaust ventilation. For full specifications, visit the company online.

Terra Universal
Fullerton, CA
www.TerraUniversal.com

Complete line of corrosion-resistant furniture

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Vestilab S.A. Clean Room Control is dedicated to the manufacturing and supply of products for cleanrooms and aseptic areas in sectors such as pharmaceutical, chemical, cosmetics, research, and animal health. The company offers a wide range of stainless-steel furniture (work tables, workbenches, sinks, cupboards, step-over benches, a complete range of shelving systems and trolleys, dustbins, chairs, and more) in many models and sizes that comply with NSF requirements. Vestilab’s stainless steel is AISI 304 BA type enriched by 18 parts nickel and 10 parts chrome (18/10). The BA finish makes furnishings smooth and more resistant to corrosion.

Vestilab S.A. Clean Room Control
Barcelona, Spain
www.vestilab.com

These small consumables make an impact in big markets

By Robert McIlvaine and Betty Tessien, The McIlvaine Company

There are three broad categories of wiping products: woven flat wipers, non-woven flat wipers, and swabs. The main advantage of swabs is the variety of shapes and materials in which they are available. This makes them ideal for cleaning in very small, very precise areas.



Figure 1. A broad range of industries uses swabs for tasks in forensic DNA collection, electronics manufacturing environments, and pharmaceutical manufacturing facilities, to name a few. Photos courtesy of Puritan Medical Products Co. LLC.
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Swabs are used in applications including cleanrooms, electronics, scientific, forensic DNA collection, medical/dental, equipment manufacturing, pharmaceutical, and food testing.

Types of swabs

Swabs can be application matched and modified by the manufacturers to meet specific user needs. Parts can be either natural or synthetic. Variables include handle length and material; tip size, shape, and material; and solvent retention, absorbency, and adsorption capabilities. Foam, polyester, and cotton are some of the head material choices. The heads can be bonded thermally, folded, or melt welded. Some new heads have spirals that may grab more debris.

Polyester swabs have low nonvolatile residue qualities (NVR), low particle shedding, and are chemically resistant. A swab with a head of laundered polyester knit fabric provides low levels of releasable particles, high recovery, and low background when total organic carbon (TOC) measurements are employed as the analytical technique.

Handles can be polypropylene, nylon, glass-filled nylon, glass-filled polypropylene, wood, or styrene. Swabs vary in handle length (from 7 to 25 cm) and in head shape and size (from 4 to more than 16 mm). The handle can also be notched for easy breaking.

Solvent-safe swabs are designed for electronics manufacturing and repair. Different absorbencies are available. Packaging options are available, including ESD-safe options and cleanroom-compatible swabs. Pharmaceutical manufacturers and those using cGMPs need products that maintain sterility. Some swabs are made without the use of adhesives or binders. Puritan Medical Products Co. actually holds the patent on fluid-filled swabs, which contain a solution in a non-glass ampoule that is broken to release a solvent, often alcohol, into the swab. These are especially useful in field service to avoid cross-contamination or spilling of a solvent. Solvent contamination is always a concern.

Cleaning, validation, and standards

Swabs reach areas, crevices, and gaps that can’t be reached or cleaned with conventional methods. Once the swab picks up residue, it must be retained. Swab sampling can be considered the most widely used cleaning validation sampling technique. It is a crucial step in cleaning validation assessment. The physical characteristic of the swab and the substrate surface, as well as the physical swabbing motion, all contribute to the physical validation process. The chemical process is controlled by the dissolution of the analyte from the surface of the substrate into the wetted swab and then by the extraction of the analyte from the swab into the recovery solution. The swabbing motion needs to be standardized to assure that recoveries validated during analytical studies are replicable by those performing the swabbing. The procedure should be documented in a standard operating procedure.

There is a specific method to wet the swab head and prevent excess liquid from spreading the residue to be picked up onto the surrounding surface. Errors in technique lead to inconsistent results. The swab should be damp but not saturated. Pre-cleaned vials and swabs are available that provide TOC background levels of less than 10 ppb for solutions and less than 50 ppb for swabs.

The pharmaceutical industry uses swabs for validation as well as cleaning. Technicians swab an area as small as 1 inch by 1 inch for surface validation. These swabs often have handles that break so the swab can be place in a container with media to extract the particles from the swab.

WG-CC025: Evaluation of Swabs Used in Cleanrooms is a recommended practice published by IEST. It describes methods for testing swabs used in the cleanroom and other controlled environments for characteristics related to both cleanliness and function.

Cost

Swab prices range from less than $0.10 to more than $0.30 each. Often swab choice depends on the size of the particle that is of concern and whether it will create loss of yield. After swab features such as bioburden levels, absorbency, adsorption, particle counts, and pre-saturation, competition often comes down to pricing. Foam swabs can be more economical, and many still contain no adhesives.

Manufacturers

Manufacturers are often located where labor is cheap, such as in Asia or China, or in a place where the white birch wood for handles is readily available. Some of the largest U.S. manufacturers are located in Maine, Colorado, and Wisconsin.


Figure 2. A swab developed for use in the aerospace industry features a flexible paddle tip made of laundered micro-fiber. The absorbent micro-fiber is well suited for working with lenses and optics because it leaves no lint or residues, and both the handle and the tip are chemical resistant. Photo courtesy of Puritan Medical Products Co. LLC.
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Chris Collopy, sales manager of industrial products at Puritan Medical Products in Maine, says that the company has been manufacturing since 1919. It has introduced 17 new styles for use in the critical environment, including a micro-fiber product that offers wipe/dry characteristics especially important to the optics arena. The company offers a folded and twisted swab with no seams or edges that doesn’t generate particles. It has also recently produced a sonically welded swab specifically requested by and manufactured for the aerospace industry (see Fig. 2).

According to Collopy, the flexible paddle tip is made of laundered micro-fiber. The NVR swab results show 0.003 mg/swab. The absorbent micro-fiber is excellent for lenses and optics, leaves no lint or residues, and both the PP handle and tip are chemical resistant, he notes.

Powell Products, a manufacturer of swabs and transfer devices that was founded in 1959, has more than 110 employees and manufactures 160 million swabs per year in its Colorado Springs, CO, facility and another 20 million in Mexico.

Market trends

The worldwide cleanroom wipers and swab market totals more than $600 million. These are annual sales calibrated by the end purchasers’ payments. The cleanroom swab market is presently estimated at $70 million worldwide with a growth rate of eight percent projected over the next five years.

The 10 leading purchasers of swabs by country are:

  1. United States
  2. Japan
  3. South Korea
  4. Taiwan
  5. China
  6. Thailand
  7. Malaysia
  8. United Kingdom
  9. Philippines
  10. Germany

The swab market in China will grow faster than in any of the other top 10 countries. Thus over the next decade, China will move near the top of the purchasing countries.

The semiconductor industry will continue to be the main purchaser, but the flat-panel display and other segments will grow faster.

Manufacture will be increasingly global with a few suppliers dominating the worldwide market. Low cost regions will be selected for future manufacturing facilities. Distribution will be broad with many international distributors providing the products in various regions.

Michael Balestri, category manager at VWR, notes the swab market has been driven lately by TV shows such as “CSI (Crime Scene Investigation).” The shows have actors using new, state-of-the-art swabs; real swab users then ask for similar products. This has increased the trend for swabs with containment caps on the ends (refer to Fig. 1 for an example) and for individually wrapped swabs. According to Linda Grassia, marketing manager of Qosina, a new swab Qosina offers has a polypropylene vented cap that slides down a wood shaft to allow sampling, then slides back to cover the swab head with a snap-on cap.

A noted market trend is the individually sterile wrapped swab. These are often used in medical applications. ETO sterilization is frequently used for these swabs. Other cleaning devices and materials that used to be hand-held, such as surgical scrubs and solutions, are being put on the end of a swab to avoid cross-contamination, even if a glove is used.

The electronics industry holds a large share of the swab market. This segment is less likely to shop around but sticks to a tried and true swab, according to one vendor. In the flat-panel and circuit board industries, swabs are used to clean space not accessible by other cleaning methods, inside orifices or tubes. In semiconductor manufacturing, swabs are needed to clean O-ring chambers before the device is sealed. However, static is a huge issue in the electronics industry, such as in hard disk drive manufacturing. Even a minute amount of static can render a product useless. Often a swab is dipped in an alcohol solvent that is placed on a static discharge mat and the user wears static discharge wrist straps. Handles on the swabs are also often made to dissipate static. Some of the newest swabs contain carbon black or inherently static dissipative-polymers for this purpose. “It is important that the swab handle allows a path to ground as well as being low in tribo-charging properties. The use of carbon powder allows for fast static dissipation while the inherently static-dissipative handles allow for a controlled path to ground and low particulate and contamination potential,” says Kurt Edwards, sales and marketing manager for Lubrizol Conductive Polymers (formerly Stat-Rite). The company’s Stat-Rite® IDP alloys are currently being used by several ESD/cleanroom swab manufacturers for swab handles.

Another development is a split head swab. This is especially useful in cleaning both sides of a tube or cable. Other application-specific swab head shapes and sizes are being manufactured. High-Tech Conversions offers a large 16-inch swab with a very large head called a “lollipop” swab.

Another growing market is swabs used in the cosmetic industry, not only for production but also for applications at home. Because of the ability to change the shape of the tip for various applications, they are more desired than the older brushes. They are cheaper and can be replaced often for better hygiene.

Micro-fiber is a non-woven, ultra-fine, durable synthetic fiber, which can be made from polyester, acrylic, nylon, rayon or a blend of these materials. Micro-fiber offers a huge surface area. It has been shown to clean with no solvents or detergents, has no organic shedding, and is durable. It holds a tremendous amount of liquid by high adsorption. Swabs and wipers are now being made of this material.


Robert McIlvaine is president and founder of The McIlvaine Company in Northfield, IL. The company first published Cleanrooms: World Markets in 1984 and has since continued to publish market and technical information for the cleanroom industry. He can be contacted at [email protected].

Betty Tessien is the cleanroom publications editor for The McIlvaine Company. She can be contacted at [email protected].

Acknowledgments

The following individuals provided industry and product information: Michael Balestri, VWR; Chris Collopy, Puritan Medical Products; Kurt Edwards, Stat-Rite; Charles Garber, SPI Supplies; Linda Grassia, Qosina; and Claudio Orefice, High-Tech Conversions.

New Products


July 1, 2007

Compiled by Carrie Meadows

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Class 100 cleanroom cabinet oven
The No. 971 is an electrically heated, 500°F (257°C) Class 100 cleanroom cabinet oven from Grieve, used to sterilize glassware at the customer’s facility. Workspace dimensions measure 36 x 36 x 39 inches. A 1,200 CFM, 1-1/2 horsepower recirculating blower motor provides horizontal airflow to the workload. For Class 100 cleanroom compliance, this cabinet oven has a 12 x 12 x 6-inch thick HEPA fresh air filter with 2-inch prefilter and a 30 x 24 x 6-inch thick stainless-steel, high-temperature HEPA recirculating filter.

The Grieve Corporation
Round Lake, IL
www.grievecorp.com

Port fitting, combo strainer/ball valve

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Victaulic has added the Tour & Andersson Series 78U Union Port Fitting and Series 78Y Strainer/Ball Valve Combination to its product line for measuring and balancing flow rates. The port fitting features a port section equipped with a manual air-vent port on top, allowing for optimal positioning at the coil outlet and effective venting together with a pressure/temperature port on the side. The strainer/ball valve combination helps protect both coil and modulating valve from pipe scale, sand, or weld slag. The valve combination consists of a stainless-steel strainer, a blowout-proof valve stem, Teflon® packing, plated ball, and a strainer-blowdown and drain valve with hose thread, cap, and retainer. Both products are available in 1/2 to 3/4 inch versions. They are pressure rated up to 400 psi/2,758 kPa and can withstand temperatures up to 250°F (120°C).

Victaulic
Easton, PA
www.victaulic.com

Filters for recirculation, FFU applications

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Process, contamination control, and quality assurance engineers can minimize AMC-related defects with cleanroom-compatible filters from Purafil. The Purafilter®-CG and the Purafilter®-FFU use Purafil’s patented dry-chemical media to target specific groups of gases in specific areas of cleanrooms. The filter media permanently remove AMC by transforming the gases into harmless solids. Both filters are also available with or without an integral 95% (MERV 15/EU8/F8) particulate filter. Third-party testing verifies that the filters do not contain materials that produce chemical contamination, nor do they outgas trace metals or dopants. The Purafilter-CG works in recirculation air applications, and the Purafilter-FFU can be incorporated into most FFUs upstream of HEPA/ULPA filters; both are available for various media types.

Purafil
Doraville, GA
www.purafil.com

Fabric-faced diffuser

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DuctSox®, a manufacturer of U.S.-made fabric duct systems and accessories, has introduced the D-Fuser™, the HVAC industry’s first fabric-faced diffuser for research laboratories, pharmaceutical manufacturing, and other critical environments. The D-Fuser features an environmentally friendly, 50 percent recycled polyester fabric face with an antimicrobial treatment. A trim kit is available for finished ceiling retrofits. It is immediately available in three models: Lami-Flow-vertical dispersion through fabric porosity; Radial Flow-radial dispersion, fabric porosity, and venting; and Select Flow-fabric porosity and custom venting. The D-Fuser’s face-frame is easily disengaged without tools, via six quarter-turn fasteners, for sanitizing or quick airflow direction change-outs. Retrofit kits will also become available to allow customers to outfit their existing backpan with one of the three available models.

DuctSox®
Dubuque, IA
www.ductsox.com

Modular workstation with conveyor system

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Lista International Corporation presents the Arlink® 8000 Modular Workstation System with conveyor solutions. Ergonomically designed, these modular workstations offer flexibility to accommodate changing or future needs. Suitable for a variety of applications, such as assembly, inspection, testing, rework, packaging, and material transfer, the workstations are also available with a supplied conveyor system or easily integrated with an existing conveyor for cost-effective, high-efficiency workflow management through the entire production stream. The Arlink 8000’s Definite Positioning System™ makes relocating or adjusting worksurfaces, storage, shelving, lights, power beams, footrests, and more fast, easy, and safe. Worksurfaces are available in standard laminate or static dissipative.

Lista International Corporation
Holliston, MA
www.listaintl.com

Small-volume drug sampling system

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The new NovaSeptum AV Accurate Volume system from Millipore is designed to meet the requirements for aseptic and sterile sampling of biotherapeutic products. The closed, accurate sampling system enables production personnel to obtain small-volume product samples easily and efficiently without the risk of cross-contamination. This level of accurate sampling eliminates the aliquoting step, further reducing the risk of cross-contamination. The ability to dispense product with milliliter accuracy improves sampling efficiency while reducing potential product waste. The NovaSeptum syringe can also be stored until sample testing is required. The drug product and sample are always enclosed in a sterile, closed environment. The risk of false positives is eliminated and the safety of the product, sample, and operator is ensured.

Millipore Corporation
Billerica, MA
www.millipore.com/bioprocess

Luminescent oxygen sensor

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The G1100 Trace Oxygen Sensor from Hach Company is the first sensor for ppb level oxygen monitoring that uses luminescent dissolved oxygen (LDO) technology. Design for maximum reliability and minimal maintenance, the sensor offers advantages over DO sensors with traditional chemical cells: no electrolyte, chemicals, or complex service procedures are required; it incorporates automatic on-line calibration; real-time diagnostics are provided; and service requirements are limited to just five minutes every 18 months, according to the company. It features a detection limit of 0.01 ppb and measures DO in the range of 0 to 20,000 ppb.

Hach Company
Loveland, CO
www.hach.com/power

Powder-free textured gloves

Tronex Nitrile powder- and latex-free textured examination gloves are manufactured to provide highly reliable protection and effective resistance against chemicals and sharp objects. They meet the ASTM 739-99 Chemo Rating and exceed FDA (K) Requirements, as well as satisfying other leading manufacturing standards. The gloves offer a high degree of tensile strength and elongation; ultra-low modulus formulations allow tactile sensitivity, flexibility, and dexterity for reduced hand fatigue in the health care and pharmaceutical industries. Sizes small, medium, large, and extra large are available in boxes of 50 (10 boxes per case for a total of 500 gloves).

Tronex Healthcare Industries, a division of Tronex Company
Parsippany, NJ
www.tronexcompany.com

Tabletop filler and capper for ophthalmics and topicals

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The FF30 Bottle Handling System from Flexicon America moves from liquid fills to handling viscous ointments, gels, or creams simply by attachment to the appropriate dispensing pump. Liquid fill materials within the PF6 are completely isolated within the replaceable sterile silicone tubing. For more viscous materials, the Tabletop FF30 is simply moved into place and paired with the quick calibrating, simple-to-clean DF32 Positive Displacement pump head. The pump generates no flow pulsation and does not interfere with homogeneous products. Depending on viscosity, fill volume, and container size, bottles can be filled at speeds of up to 1,200 fills per hour. Liquids can be filled in volumes from 0.1 to 100 ml, and creams can be filled in volumes from 10 to 5,000 ml.

Flexicon America Inc.
Burlington, VT
www.flexiconamerica.com

Energy-saving high-intensity fluorescent lighting

Orion’s high-intensity fluorescent (HIF) systems and controls replace the standard high-intensity discharge (HID) lighting fixture. HIF systems deliver an average of 50 percent more light at half the energy usage compared to HID lighting fixtures. Products include the Compact Modular T8 Series, a high-bay lighting series designed for industrial, distribution, and warehousing applications; the T8 Enclosure Series, designed for freezer applications; and Conversion Kits designed to upgrade conventional 4-foot T12 strip fixtures. A patented aluminum “I” frame dissipates heat at a much higher rate than steel, lowering the temperature surrounding the ballast and increasing its expected life. Orion lighting products are designed to comply with or exceed all UL requirements.

Orion Energy Systems
Manitowoc, WI
www.oriones.com

Programmable syringe pump

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The Harvard Apparatus PHD 400 programmable syringe pump has a high-power stepper motor that provides more than 200 lb. of linear force. Using a 2.5 ml stainless-steel syringe, the user can achieve pressures up to 8,000 psi for applications such as micro-reactor delivery, drug delivery, working with highly corrosive materials, and high-pressure reactors. The PHD 4000 can run continuously in pump mode, dispense a specific volume in volume mode, or run multiple sequences in program mode; sequences can be stored in the non-volatile memory for future use.

Harvard Apparatus, Inc.
Holliston, MA
www.harvardapparatus.com

Utility software for airborne particle counters

Biotest has released the APCOne11-21 CFR Part 11 compatible-Download Utility Software for its line of airborne particle counters. The tool allows the user to safely transfer data from the particle counters to a computer without compromising data validity. The secure electronic transfer reduces operator error and meets FDA standards for data protection. It also has an audit trail to log critical events, password protection features, and digital signature application for file authentication.

Biotest
Denville, NJ
www.BiotestUSA.com

Extended-life contactors for IC testing

inTEST Corporation, a developer and manufacturer of equipment for semiconductor testing, has introduced V-Touch™ Extended-Life™ Contactors featuring more precisely aligned spring pins, with critical feature machining tolerances that are tighter than those of conventional products (less than 0.0003 inches, approximately 0.6 microns). Proper spring pin alignment is critical for repeatable electrical measurements and minimizing false negatives (the rejection of good ICs). The V-Touch designs, which incorporate DuPont’s state-of-the-art Vespel® polyimide, deliver longer cycle life than conventional contactors. The organic polymer is known for its low wear, excellent creep resistance, impact resistance, and strength. Because inTEST optimizes the design for each probe structure, customers are free to use whatever spring probe they prefer for their test.

inTEST Corporation
Cherry Hill, NJ
www.intest.com

Accepting USP <797>as a robust quality and patient safety regulation is the first step to enforcing it

By Eric S. Kastango, MBA, RPh, FASHP

What do all these situations have in common?

  • A 25 bed critical-access hospital in rural Minnesota
  • A physician’s office where intramuscular antibiotics are given to children with pneumonia
  • An allergist who manages the care of 200 patients with allergies
  • A floor nurse who compounds medications to be given to patients in critical care
  • A homecare company with 72 pharmacies in 44 states delivering home infusion therapy to more than 10,000 patients daily
  • A national outsourcing company that is both licensed as a pharmacy and registered with the FDA as a manufacturer

Unlike pharmaceutical manufacturing, where companies are more similar than dissimilar (though some would strongly disagree), the standards of sterile compounding must be applied to all of the situations listed above and others that were not described.

In the introduction of USP Chapter <797>, it is stated that the standards are intended to apply to all persons who prepare compounded sterile preparations (CSPs) and all places where CSPs are prepared, e.g., hospitals and other health care institutions, patient treatment clinics, retail pharmacies, physicians’ practice facilities, and any place where CSPs are prepared, stored, and transported. Persons who perform sterile compounding include pharmacists, nurses, pharmacy technicians, and physicians, and all are required to comply with this chapter.

USP Chapter <797> first appeared in the pharmacy lexicon on January 1, 2004, spawned by patient incidents starting in the 1970s. It was the genesis of years of voluntary practice standards attempting to prevent future errors. The process started with the National Coordinating Committee on Large Volume Parenterals (NCCLVP), which led to the American Society of Health-System Pharmacists Guidelines on Quality Assurance for Pharmacy Prepared Products in 1993, USP Chapter <1206>: Sterile Drugs for Home Use in 1995, and to the present day chapter, which is considered enforceable by the FDA.

Now that we are into this enforceable chapter for more than three years, how did the USP Council of Experts, Sterile Compounding Committee do? Well, if you ask the hundreds of stakeholders who submitted thousands of comments including several prominent organizations like the Centers for Disease Control (CDC), the American Society of Microbiology (ASM), Association for Professionals in Infection Control and Epidemiology, Inc. (APIC), and the FDA, there was opportunity for improvement. Since the USP process is a dynamic one and relies on stakeholder feedback, a revised chapter is scheduled for release in 2007.

The revised chapter was written to consider all of the perspectives of the various groups, some of which are at odds with the standards of practice expected of pharmaceutical manufacturers and by the FDA.

Some of the principles, concepts, and requirements within the revised USP Chapter <797> have been challenged by the question “Where is the science behind the requirements?” Many pharmacists and other stakeholders believe that the requirements are too stringent and have questioned their need especially in the areas of facilities, environmental monitoring, personnel garbing, and cleaning and disinfection. These sections involve spending money in areas that have historically been misunderstood, overlooked, ignored, or routinely de-funded. In the pharmaceutical industry, many of the thought leaders and even the editor of this publication have stated that they believe the chapter is not stringent enough. Aseptic processing in the practice of pharmacy is, most of the time, not the same as manufacturing. However, there are parallels with many of the same practices, processes, and procedures. There are several factors that make this chapter as a “one-size-fits-all” regulation tenuous. They include:

  • Many pharmacists by choice or by necessity have to handle and compound patient-specific sterile preparations using bulk non-sterile active pharmaceutical ingredients in order to meet the patient’s therapeutic needs because no commercial drugs are available. When does the pharmacy cross the line and become a manufacturer?
  • Patients won’t be able to access care because the cost of compliance will discourage practitioners in rural areas who only compound a few CSPs per week. At what point does a practitioner have to comply with the regulations?
  • Some state boards of pharmacy permit pharmacists to compound non-patient-specific sterile preparations for office use (bulk vials), making some pharmacies appear more like manufacturers. This flies in the face of federal regulations. Do these pharmacies have to comply with different standards?
  • The ongoing tug of war between the FDA, compounders, and state boards of pharmacy in identifying the point at which a compounding pharmacy becomes a manufacturer spurred the FDA to post on May 31, 2007 a document titled “The Special Risks of Pharmacy Compounding” (http://www.fda.gov/consumer/updates/compounding053107.html) on its Consumer Health Information Page.

Some would argue that these situations don’t make the matter of compliance very easy or clear. However, with all of that being said, is there an easy answer to the “one-size-fits-all” regulation? I think so. As the new revisions get assimilated into practice, and everyone starts believing that the moving target known as USP Chapter <797> isn’t moving any more, the excuses as to why people can’t comply will go away. It is a robust document with the express purpose of building quality into compounded sterile preparations and ensuring patient safety. This chapter will continue to spark the scientific research that will, in turn, generate the scientific evidence needed in the area of sterile compounding.

The bottom line is that USP Chapter <797> is a regulation that is not going away and compliance is required. Unlike registered manufacturers who have the FDA to enforce the cGMPs, not all state boards of pharmacy are on board with this regulation yet. It is my hope that the state boards will rise to the challenge and take responsibility for this chapter and start enforcing it in order to ensure patient safety and keep the FDA out of the practice of pharmacy.


Eric S. Kastango is president, CEO, and owner of Clinical IQ LLC, a provider of customized process and educational strategies for the pharmaceutical, medical device, and health care industries. He also serves on the CleanRooms Editorial Advisory Board.

By George Miller

Despite the highly publicized antics, a poorly attended biolab protest may have done more to illustrate the growing acceptance of Biosafety Level 3 and 4 facilities-even in urban areas-than to rile up residents. It also provided a reminder to lab managers of the importance of maintaining relationships with the communities in which they reside.

The lackluster effort, intended to protest a BSL-4 laboratory now in the final stages of construction at Boston University, coincided with the huge Biotechnology Industry Organization (BIO) trade show in Boston in early May.

At a time of growing competitiveness among state and local governments to attract biotech business, and among academic and medical institutions to win government research contracts, the likelihood of a BSL-3 or -4 lab popping up in a city setting or suburban neighborhood is on the rise. And in these days of color-coded terrorism threat levels, more residents are beginning to understand the need for infectious disease research, which is required whether disease is spread by terrorists or Mother Nature.

Boston University’s $178 million National Emerging Infectious Diseases Laboratories BSL-4 facility is one of several being built with funding from the National Institute of Allergy and Infectious Diseases (NIAID), part of the U.S. National Institutes of Health (NIH), in an effort to bolster United States biodefenses. BU Medical Center will receive $128 million in federal funds for the project, which is expected to be complete next year.

Document standardizes operating procedures

Legislation approved in 2003 calls for the NIH to establish national and regional biocontainment labs as well as regional centers of excellence for biodefense and emerging infectious disease research. A national-level guidance document, Biosafety in Microbiological and Biomedical Laboratories (BMBL) 5th Edition, provides operations and protocol details and is available at the U.S. Centers for Disease Control and Prevention web site (www.cdc.gov).

“All of our grantees are required to follow this guidance, as well as state and local requirements,” says Rona Hirschberg, senior program officer at the Office of Biodefense Research Affairs, NIAID.


National and regional biocontainment laboratories (top) support the research activities of NIAID’s regional centers of excellence (bottom) for biodefense and emerging infectious disease research. The biosafety labs also will be available to assist national, state, and local public health efforts in the event of a bioterrorism or infectious disease emergency, according to NIAID. Source: NIAID.
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Given a standard for operating BSL-3 and -4 facilities, the community relations job becomes one of transparency-letting the public know what you’re doing and that systems are in place for residents to be informed of mishaps and for authorities to respond.

Strained relations

Since NIAID awarded BU a grant to build its lab in 2003, the university’s relationship has been rocky with its neighbors in Roxbury, a low-income, densely populated part of Boston’s South End. In response to community actions, BU and NIH are currently conducting a second environmental impact assessment and alternative site evaluations for the BSL‑4 portion of the lab, even as construction continues on the building’s façade and interior. Residents’ opposition to the lab may have been fueled by a contamination incident in 2004, when three university researchers working in a BSL-2 lab were infected after exposure to tularemia. BU acknowledged that the researchers had violated safety procedures.

Historically, biosafety labs have an excellent safety record. Hirschberg of NIAID cites the safety studies of Karl M. Johnson, MD, adjunct professor of medicine and biology, at the University of New Mexico-Albuquerque, on the long-term safety records of BSL-3 and -4 facilities. As part of an environmental impact statement prepared prior to construction of a lab at Rocky Mountain Laboratories, Johnson, the retired founding chief of the CDC’s Special Pathogens Branch, reported in 2003 that no clinical infections occurred over 31 years at the three BSL-4 institutions studied. The study period reflected nearly half a million hours of lab and field exposure time, the majority spent in positive-pressure suits. No major defects or incidents in operation of the physical facilities were reported. No escape of any agent with clinical consequences for neighboring communities occurred.

In a separate study of BSL-3 labs, Johnson likewise found that no agent had escaped to cause infection in adjacent civilian communities.

Community needs view into lab ops

Those running such labs agree that a clear view into lab operations is key to community acceptance. “The number one [job] is transparency and keeping the community fully informed,” says Hirschberg.

At the Howard T. Ricketts Regional Biosafety Lab in Chicago, research operations manager Debra Anderson has adapted a community relations template established more than half a century ago for nuclear energy research. The lab’s work is temporarily being conducted at the University of Chicago. When a new facility is completed in 2008 some 25 miles southwest at Argonne National Labs-where Enrico Fermi led the first controlled nuclear chain reaction in 1942-biosafety lab operations will shift there, to be co-located with NIH’s Great Lakes Regional Center of Excellence for Biodefense and Emerging Infectious Diseases.

“We’ve designed a community relations plan that models Argonne’s historical methods: very transparent, very active,” says Anderson, who is also associate director of the Great Lakes Regional Center of Excellence. “If you’re not transparent, it’s easy for assumptions to be made [by the public],” she adds.

Outreach addresses common fears

Ricketts Lab outreach has done a lot to calm community fears, Anderson notes. Organizers of the $31 million BSL-3 lab created a committee to advise the University of Chicago on outreach strategy and topics of interest to the community. “The committee has been very valuable and was recently formalized,” she says. “What we hear routinely is, ‘How will we know if there’s a problem? Will physicians know?’ You get to see [residents’] understanding of containment safety levels. We’ve provided education and it’s been well received.”

Direct contact with residents is also working at Tufts Cummings School of Veterinary Medicine. The school is building a $26 million BSL-3 regional biocontainment lab in Grafton, MA, a town of 15,000 residents located 40 miles west of Boston. Completion is estimated for August 2009.

A community advisory group provides a means for quarterly public discussion between Tufts and Grafton residents. It is the Cummings School’s “key connection to its neighbors,” said interim dean Sawkat Anwer, providing dialogue between the campus and the community.

Tufts established several community boards in its outreach efforts, according to Anwer, and has participated in town-sponsored boards and committees. The school also works with the Grafton liaison group on local government issues and an institutional biosafety committee to meet regulatory requirements.

SEMICON WEST 2007


July 1, 2007

JULY 16-20, 2007 MOSCONE CENTER, SAN FRANCISCO, CA

EVENT HOURS
Exhibits

Tuesday, July 17-Wednesday, July 18 10:00 a.m.-6:00 p.m.
Thursday, July 19 10:00 a.m.-4:00 p.m.

Conference program runs from Monday, July 16, through Friday, July 20

SEMI, the global industry association serving the semiconductor manufacturing supply chain, is hosting its 37th annual SEMICON West Conference and Exhibition from July 16-20. Attendees will have the chance to learn about the latest developments in nanoelectronics, MEMS, test and packaging/assembly, wafer processing, and more. For a complete conference schedule, visit www.semi.org.

SHOW HIGHLIGHTS

The President’s Reception
Monday, July 16, 6:00-7:00 p.m.
At the President’s Reception, connect with global industry leaders and experts and cultivate new contacts.

Opening Keynote:

“Distributed Innovation: Leveraging Collaboration for Competitive Advantage in Semiconductor Manufacturing”
Tuesday, July 17, 9:00-10:00 a.m.
AMD’s senior vice president of technology development, manufacturing and supply chain, Douglas Grose, will address the need for collaborative innovation in the semiconductor industry as a result of rapidly rising costs, outlining the competitive advantages and different models for successful collaboration.

ITRS 2007 Public Conference

Wednesday, July 18, 8:00 a.m.-5:45 p.m. (Networking Social 5:45-7:00 p.m.)
The International Technology Roadmap for Semiconductors (ITRS) celebrates its tenth year as the first international roadmap for any industry with an opportunity for public participation during the ITRS working group presentations of draft material for the latest revision.

SEMICON West Standards Meetings

Monday, July 16-Friday, July 20 (generally between 8:00 a.m.-5:30 p.m.)
Topics for standards issues abound, from electrostatic discharge prevention to equipment productivity measurement to factory automation standards.

EXHIBITOR SHOWCASE

More than 1,300 leading companies and suppliers connected to the semiconductor manufacturing industry will display their innovations at SEMICON West 2007. Here are a few that will be of interest to the contamination control community.

Anticon Products by Milliken

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Web: www.anticonwipers.com
Booth 6242
Anticon® Products by Milliken introduces its newest wipers with Particle Attraction Technology (P.A.T.). Anticon wipers with P.A.T. (top) capture up to 35 times more particles than traditional wipers (bottom) and retain 95 percent of particles captured, reducing the risk of recontamination. The wipers arrive cleaner: A vertical manufacturing model, in the industry’s only ISO Class 1 at 0.1 micron facility for wiper production, ensures rigorous standards for cleanliness are met across all manufacturing steps. The wipers are available in a variety of fabric bases, sizes, and weights, used with solvents or for dry wiping.

Asahi/America

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Web: www.asahi-america.com
Booth 114
Engineered to meet the advanced wet process requirements of the semiconductor industry, the Dymatrix™ specialty valves line includes pinch valves, diaphragm valves, needle valves, and pressure regulators that are suited for CMP slurry, DI water, and chemical process applications. The durable pinch valve eliminates particle generation in CMP slurry applications. The diaphragm valves are engineered for high cycle life and compact design. The needle valve utilizes a dual stem for true linear flow control and integrated diaphragm for excellent purity. The pressure regulators are designed to provide accurate and highly stable control of pressure fluctuations for flow control applications.

BOC Edwards

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Web: www.bocedwards.com
Booth 730
BOC Edwards is a leading provider of support equipment solutions for the semiconductor, solar, and flat-panel display industries. The company’s technical experts work closely with leading process system manufacturers to develop innovative products required to meet critical performance challenges. The global service network ensures local support around the world. BOC Edwards will be showcasing its latest products: dry vacuum and turbo pumps, exhaust gas management, and component cleaning parts.

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DuPont Controlled Environments

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Web: www.dupont.com
Booth 1906
DuPont is dedicated to the science of protection. The goal of DuPont Controlled Environments is to provide high-performance solutions for today’s demanding controlled environments. Combining scientific innovation and material, garment and manufacturing expertise, DuPont Controlled Environments products are specially engineered to enhance productivity in today’s demanding biotechnology, pharmaceutical, medical device manufacturing, and electronics cleanroom environments. The company offers a wide range of protective garments and products, including DuPont™ Tyvek® IsoClean™ garments for premium protection, DuPont™ Suprel® LS for a balance of comfort and protection, and a range of accessories such as DuPont™ Gripper™ shoe and boot covers with superior coefficient of friction properties. In addition, DuPont Controlled Environments specialists are industry experts who can help with site assessment and a variety of contamination control issues to help ensure each critical environment is as efficient as possible.

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Entegris, Inc.

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Web: www.entegris.com
Booths 1020 and 1114
Entegris provides high-performance products and solutions that purify, protect, and transport the critical materials that are essential to the world’s semiconductor manufacturers, OEMs, and materials suppliers. Using its market and technological leadership in materials science and micro and molecular contamination control, Entegris helps its customers enhance their yields and improve their productivity along their technology roadmaps. Featured products at SEMICON West will include Clarilite certified reticle haze prevention system (booth demo); IntelliGen® mini two-stage-technology dispense system (booth demo); LiquidLens™ UPW purification system; QuickChange® ATE 30 nm non-dewetting Teflon® filter (shown); PVA brushes; front-opening shipping box (FOSB); Spectra™ front-opening unified pod (FOUP); 300 mm multiple film frame shipper; and Ultrapak® edge guard wafer shipper.

Kimberly-Clark Professional

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Web: www.kcprofessional.com
Booth 2967
Kimberly-Clark Professional offers a dispenser for pre-saturated alcohol wipers that provides convenient, one-handed dispensing with no need to hold a package or re-seal a closing flap. The new KIMTECH PURE* Dispenser makes cleanroom wiping easier than ever before. A self-closing, self-sealing lid helps prevent dry-out of wipers, eliminating waste. An innovative extractor arm automatically lifts each wiper for easy pickup without damaging the wipers. The dispenser also features a durable design that does not generate particles and makes refilling easy.

Kinetic Systems, Inc.

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Web: www.kineticsystems.com
Booth 6543
The 9600 Series Class 1 cleanroom-compatible vibration isolation workstation from Kinetic Systems, Inc. is designed specifically for cleanrooms and uses proven performance characteristics from KSI’s standard line. Electropolished stainless-steel welded tubular braces, enclosed isolation modules, stainless-steel valves, vented exhaust, low natural frequencies, and high isolation efficiencies provide an ideal Class 1 cleanroom match.

Lighthouse Worldwide Solutions

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Web: www.golighthouse.com
Booth 6355
Using patent-pending technology, Lighthouse Worldwide Solutions has created the smallest sequencing particle counting manifold system in the industry. When connected to Lighthouse particle counters, the 1 CFM Mini Manifold™ is the best-in-class solution for tool monitoring and qualification, minienvironment monitoring, and even portable, cart-based monitoring systems. The 1 CFM Mini Manifold™ consists of a manifold sequencing system with a built-in controller and a miniblower for purge flow. The controller communicates with the particle counter and can interface to a computer system or process tool.

MKS Instruments

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Web: www.mksinst.com
Booth 1720
MKS Instruments, Inc. will exhibit the CONTINUUM™ Universal Industrial Network Gateway with cLogic™ and the MacroNode™ I/O Controller with EtherCAT interface. These new solutions offer precise process control through faster network performance and improved web browser diagnostics. The MKS CONTINUUM quickly connects any serial device to Fieldbus and industrial Ethernet protocols, and includes cLogic technology that enables users to implement custom data translation. The MacroNode I/O now supports EtherCAT, an open real-time network, as well as Modbus/TCP™, Ethernet/IP™ and DeviceNet™.

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RASIRC

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Web: www.rasirc.com
Booth 3051
RASIRC, the Steam Purification Company, offers products that generate high flow, ultra-pure water vapor that is contaminant free and produced safely and economically using readily available DI water. Water vapor control ranges from 10 sccm to 100 slm. The RASIRC technology includes the RASIRC Steamer, the first steam purification system brought into the semiconductor market. The RainMaker Humidifier features a non-porous membrane for controlled humidification of clean air or other process gases while preventing contact between the carrier gas and water. This “bubbleless bubbler” technology is stable, accurate, and repeatable from 10 sccm to 10 slm.

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Scott Specialty Gases

Web: www.scottgas.com
Booth 6155
The Electronic Materials Group of Scott Specialty Gases is a world leader in the development and supply of high-performance specialty gases to semiconductor, TFT-LCD, optical, MEMS, and related industries. Products include Omega Class™ dopants, enhanced HBr, CO2, NO, and many other gases that eliminate raw material waste and process retuning, and speed product time-to-market. Scott maintains strategically located ISO 9001:2000 certified manufacturing facilities and distributes products throughout North America, Europe, and Asia.

Technical Manufacturing Corp.

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Web: www.techmfg.com
Booth 6456
Technical Manufacturing Corporation (TMC) designs and manufactures precision vibration isolation systems for sensitive research and manufacturing processes worldwide. Its STACIS® 2100 is a six-degrees-of- freedom active cancellation system employing geophones to sense ambient building floor vibration. Piezoelectric actuators drive the payload with equal and opposite force to cancel vibration from 0.6 to 250 Hz. STACIS allows precision metrology and lithography tools to be located in noisy environments and still meet tool manufacturers’ floor vibration criteria. The Electro-Damp® II active pneumatic vibration-damping system is ideal for tools that incorporate X-Y stages. The Gimbal Piston™ air isolator provides extremely effective vibration isolation, and the force motors provide aggressive damping of X-Y stage-induced motion, resulting in minimum payload motions, rapid settling time, and higher tool throughput.

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TREK, Inc.

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Web: www.trekinc.com
Booth 7256
TREK provides instruments and expertise for ESD management, ionizer evaluation, and materials research, including charge-plate monitors, electrostatic voltmeters, surface resistivity meters, electrostatic sensors/monitors, and charge-to-mass test systems. The company also offers ESD seminars and surveys. TREK’s new Model 900 ESD event detector is a diagnostic tool for ESD-sensitive environments, specifically for charge device model (CDM) events. The new Model 520A hand-held electrostatic voltmeter accurately measures surface voltage over a wide range of probe-to-surface spacings. It enables inspection of small spots for static charge accumulation and also measures charge accumulation in difficult-to-reach locations. TREK will hold an Exhibitor Showcase on July 18 at 10:30 a.m., Room 113.

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Going for the green


July 1, 2007

By Hank Hogan

Semiconductor wafer fabs tend to be one color, but now the industry wants another-green. At one of two back-to-back meetings held in mid-May in Austin, TX, members of the International SEMATECH Manufacturing Initiative (ISMI) agreed to draft a green fab standard, one designed expressly for semiconductor manufacturing. In the other workshop, ISMI members compiled a list of best practices to conserve energy in current fabs.

By going green, the industry could save substantial sums of money, notes ISMI’s environment, safety, and health technology project manager James Beasley. Estimates are that a one percent reduction in energy use in a standard facility can save $100,000 annually. “For the larger facilities, it may be even more. As the trend is toward ever larger facilities, there’s even more gain,” he says.


Even though figures show the semiconductor industry consuming only 1.8 percent of total industrial energy use in 2004, the industry is going green, with plans for a green building standard suitable for high technology manufacturing facilities. Source: ISMI.
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For existing facilities, recommendations included replacing compressor-based chillers with their solid-state counterparts. The switch would save energy while improving process control. Savings could also come from idling inactive vacuum pumps and from switching to electric pump motors. Right-sizing exhaust and air handling could also save energy, along with the use of more efficient equipment.

For new facilities, one possibility would be to incorporate advanced HVAC and heat recovery technologies. High-efficiency lighting could be another area that pays off.

One of the reasons why the industry is coming up with its own guidelines is that the Leadership in Energy and Engineering Design (LEED®) rating system established by the U.S. Green Building Council is intended for office buildings and the like. A wafer fab, assembly and test site, or flat-panel manufacturing plant is not your normal office building.

“A technology facility uses more ventilation, more energy, more water, and more resources per square foot than the typical building,” says Beasley.

Plans call for the new standard to complement LEED®, with specific additions that address the semiconductor area. The goal is to complete a draft and present the proposal to the council this year, with implementation in 2008.

Paul Westbrook, sustainable development manager for Texas Instruments (Dallas, TX), notes that TI ran into some issues regarding the current standard when the company constructed a LEED® certified facility in Richardson. With that fab commissioned and awaiting tool installation, Westbrook is now working on doing something similar in a test and assembly facility in the Philippines.

When going green, there are a number of similarities between a wafer fab and a test area. Both are controlled contamination environments, although fabs at ISO Class 3-5 are much more stringent in terms of cleanliness than ISO Class 6-8 test areas. Both have process tools, although test facilities pack in row after row of electricity-hungry probers. As a result, test areas face an added green challenge. “They can have a higher energy intensity than a cleanroom,” says Westbrook.

He adds, though, that green test and assembly areas could pay big dividends. Due to the growth in wafer size and shrinkage of devices, the number of new fabs needed won’t climb as fast as overall device output. The same, however, won’t be true in test and assembly areas.

A combination of minienvironments, thorough particle and chemical filtration systems, close environmental monitoring, and purging around key lithography steps can give operators control over contamination and improvements in yields.

By Sarah Fister Gale

Getting control of surface contamination has become the Holy Grail for semiconductor and other high-tech fab production managers intent on increasing yield and avoiding costly part replacements. With geometries dropping to the nanoscale, chemical contaminants have much greater opportunities to wreak havoc in the cleanroom and the tools than any previous generation of technology. Airborne molecular contamination (AMC), surface molecular contamination (SMC), and contamination in gases can cause problems including reticle and optics degradation, metal corrosion, resist defects, and electrical defects.

Several approaches can be used to control these problems:

  • Purifying the air using AMC filters. IEST Working Group 35 is developing standards to test AMC filters for whole cleanrooms or minienvironments.
  • Using UHP clean dry air (CDA) or inert purge gases.
  • Isolating wafers and reticles in sealed boxes to minimize air exposure.
  • Using cluster tools to complete several processes in sequence without exposing the most sensitive steps to AMC, which can cause SMC to form.
  • Using the shortest possible process queue times between the most sensitive steps. For example, nearly all production lithography tools now have coat/develop tracks directly linked to each stepper to minimize delays and AMC exposure.

Purge technologies have become one favored solution in many wafer fabs to maintain contamination levels to low parts per billion by volume (ppbv) levels or lower, especially around delicate and expensive lithography and inspection tools. But it’s not a one-size-fits-all solution. Fab operators must find the right balance of isolation, filtering, monitoring, and cost when implementing contamination control systems both for individual tools and throughout the facility.

On the surface

Geometries have shrunk so much in semiconductor manufacturing that contaminants, even at the molecular level, have the power to cause damage without any chemical or electrical reaction, says Chris Muller, technical director for Purafil, a manufacturer of air filtration systems (Doraville, GA). “Some chemical deposits are large enough to act as particles,” he says. “With device geometries of 65 nm in width and smaller, local condensation of molecular contaminants or deposition of reaction products formed between different molecular contaminants can act as a bridge, creating shorts in the circuitry. Even if it doesn’t cause corrosion, it’s still a problem.”

Understanding molecular contamination is all about identifying what’s in the air or gases and what’s causing problems on surfaces, notes Mark Camenzind, senior technical advisor for Balazs Analytical Services, a division of Air Liquide Electronics U.S. LP, which operates ISO 17025 certified laboratories that specialize in identifying ultra-trace level contamination (Fremont, CA). “Surfaces are the most common place where problems arise,” for several reasons, Camenzind says.

  • The surfaces can get degraded by SMC, such as hazing of optics, wafers, masks, and inspection tools, or corrosion of copper, aluminum, or other metallization.
  • Deposits on the surface, such as dopants, can diffuse into the substrate during high-temperature processing steps and affect electrical properties such as resistivity and threshold voltages.
  • Deposits can affect the next layer, causing epitaxial failure or defects on silicon nitride, polysilicon, gate oxide, barrier, and seed layers.
  • The top surface for one step will become the interface to the next layers. Contaminants at this interface can cause adhesion failure between layers, contact resistance, trapped charges, and magnetic defects, among other problems.

“Ten years ago, the focus for the SIA [Semiconductor Industry Association] and SEMI was on airborne contamination, but the ITRS [International Technology Roadmap for Semiconductors] is now also putting more focus on the surface and gas impurities,” Camenzind notes.

Contaminants may be combinations of organic, inorganic, ionic, or polymeric compounds. “What matters is what is on the wafer,” he says. “You have to focus on the effects contaminants have on your processes. Some contaminants don’t hurt you if they don’t impact your processes.”

It sounds simple, but identifying which contaminant, combination of contaminants, or chemical breakdowns that result in contaminants is a Rubik’s Cube that is not easily solved. For example, some silicon-containing compounds may bounce off of every surface, but when they react with ultraviolet light at 193 nm they can decompose and create compounds that will permanently deposit on the optic lens surface.

Contaminants from ambient air, gases, outgassing from purge boxes and other materials, isopropyl alcohol vapors, incoming parts and materials, and backside contamination due to maintenance can all potentially create surface contaminants that cause problems and defects. Other molecular contamination problems can occur due to plasma attack on seals, gate valves, and O-rings. Contaminants, such as ammonia, tetramethyl ammonium hydroxide (TMAH), and N-methylpyrrolidinone (NMP), are now just as significant a concern in the manufacturing environment. Ammonia, NMP, and TMAH are included in the list of bases in SEMI F21-1102 standards language and SEMATECH’s 0.25-micron process guidelines for AMC control.

Numerous sources of chemical contamination exist in the cleanroom environment; however, the challenge is in identifying which chemical or combination of chemicals is causing problems and which ones need to be filtered out. “You can’t approach this with blinders on,” Purafil’s Muller says. “There may not be a solution that is specific to a single chemical because there can be interactions with and between the multitude of contaminants commonly present in the environment.”

He believes that it is short-sighted to test the impact of individual chemicals in isolation because that doesn’t tell you what happens when they exist simultaneously in the environment. “If you focus your filtration system on a single chemical you aren’t addressing the whole problem.” For example, an ion exchange filter is excellent at removing ammonia but not at removing amines. “You may remove one problem but cause another, and that can result in additional performance loss,” he says.

At the same time, trying to filter out every chemical that is in the environment doesn’t make good financial sense. “You don’t always need lower levels of everything that may be in the air. There has got to be justification that you are getting what you need from a filter without doing too much,” Muller says. “You have to identify the right contaminant(s) and the right control levels in both the cleanroom ambient as well as in the minienvironments.”

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Muller now often encounters clients who want to reduce specific chemicals in the environment to one part per trillion (ppt) without having the information to support such a drastic approach. “Some feel that just because they are going to the next device generation, they must need to have better air quality than currently. The cost benefit has to be there. Systems can be designed to control molecular contamination to ppt levels, but just as there has to be a cost justification to do so. Just as when designing a Class 1 vs. a Class 10 cleanroom environment for particulates, there are also significant cost considerations when designing for ppt vs. ppb control levels for molecular contaminants.”

He also warns that you shouldn’t look at molecular contamination control systems as a place to cut costs. “It’s a small amount to pay compared to scrapping a day of wafer production due to a contamination incident. One day’s lost production alone can cost manufacturers millions in device losses.”

To make the best economic choices, fab operators should invest the time in identifying the cause of contamination incidents and to explore the synergistic effects of that contaminant with other chemicals in the atmosphere. “The solution may require three filters to control three specific chemicals, or it may involve a less specific ‘pre-filter’ to combat multiple contaminants at the beginning of the process,” Muller suggests. “In a Class 1 cleanroom you may go through four to five stages of particulate filtration but only one chemical filter. You can’t achieve everything you need to achieve with one filter.”

You also can’t necessarily rely on vendor data alone when judging the performance or lifespan of a chemical filter because in-house vendor testing data may not reflect realistic cleanroom conditions or testing protocols. Muller encourages companies to require third-party testing at near-ambient conditions with reports that include measurements as well as some conclusions about those measurements and what they mean. “For years we’ve preached to customers ‘don’t rely solely on the vendor for performance data’-use that as a starting point to qualify vendors, but also ask for third-party testing,” he says, noting that this will weed out the vendors who don’t have a client’s optimal interests at heart.

Once chemical filters are in, regular monitoring of their effectiveness can help avoid losses, adds Allyson Hartzell, managing scientist for Exponent, an engineering and scientific consulting firm (Natick, MA). “You can’t predict the lifecycle of a filter because of all the different concentrations of contaminants in the environment or incidents that can shorten the lifespan,” she says. “You have to be able to monitor up and downstream of filters to determine their life effectiveness.”

Purge trends

Adding more rigorous chemical filtration systems is a significant step toward managing molecular contamination for both air and gases, and these solutions work in conjunction with other contamination control tools. Additional filters on minienvironments, along with purge gases, are adding a further layer of control around extremely delicate process steps.

Enclosing process steps to reduce contaminants from ambient air is a trend that’s been steadily gaining popularity over the years because it enables fab operators to customize the contamination control necessary around critical steps in small areas while lessening controls over the larger space. Nitrogen purging is adding to the trend, as fab operators struggle to reduce the impact of surface molecular contaminants. Purging involves surrounding the process step in an isolation chamber through which ultra-pure inert gas, such as nitrogen, can be flushed, eliminating all ambient air from the optical path and exposed surfaces, and dramatically reducing the chance for surface contamination to cause problems.

“Most 300 mm and 200 mm fabs already confined wafers in front-end unified pods (FOUPs) and pods for much of their lifetime in the fab,” Camenzind says. UHP purge gases are being added as an additional control, particularly in support of the rapidly growing movement to implement deep UV (DUV) optics with shorter wavelengths to produce higher density memory and processor chips. “The shorter wavelengths, especially 193 nm, will become the workhorse of the semi fab,” Camenzind says.


Figure 2. The Entegris RSP3 Clarilite pod assists in reticle haze prevention. The arrows demonstrate that the minienvironment is being purged of potentially harmful contaminants, maintaining a clean environment for the reticle inside the pod. Photo courtesy of Entegris.
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In order to successfully employ DUV photoresist lithography, the airborne ammonia, amine, and NMP levels need to be minimized, controlled, and monitored. Most DUV photoresists are based on chemical amplification design principles, involving acid catalyzed deblocking of protective groups attached to the main polymer chain. The acid species-produced by photolysis of a photoacid generator dispersed throughout the resist film-has been found to be susceptible to neutralization by airborne-based contamination, which interferes with the propagation of the acid, and causes defects.

Unfortunately, surface contamination presents particularly challenging problems in these UV systems because most chemical species demonstrate extremely high absorption at shorter wavelengths. The effect is especially pronounced at the exposed surface of the resist where as little as 17 ppb airborne contamination of ammonia or 10 ppb N-methylpyrrolidinone has been shown to T-top resist profiles and impact critical dimensions.

“A microlithography system may contain 60 or more individual optical surfaces, so the loss of only one percent of the light per optical surface can cause the loss of about half of the system transmission,” Camenzind points out. “Surface absorption may also lower the lifetime of smaller optics that experience higher fluences.”

Tracy Niebeling, marketing manager for 300 mm solutions at Entegris, a materials integrity management company (Chaska, MN) agrees. “In 90 nm technology at 300 mm, it’s all about isolation strategies,” he says, noting that the cost of defects on reticles due to haze formation, in particular, can be particularly exorbitant. “It’s an acute problem in fabs with DUV lithography tools.” Reticle haze is formed when impurities deposit on a reticle due to the presence of molecular contaminants and moisture in the reticle environment.

Purging FOUPs with nitrogen or CDA removes airborne molecular contaminants that can potentially damage integrated circuits and significantly affect manufacturing yields. Maintaining silicon wafers in an inert environment has also been proven to enhance certain manufacturing processes and has been used to protect wafers in pods or FOUPs that are at rest on storage racks or in process queues.

To completely avoid contamination when FOUP chambers are opened, a continuous flow of nitrogen or CDA can be delivered through ports on the front end of the minienvironment using a single-pass or a recirculating system. However, that option is very costly. Most FOUPs have inlet/outlet ports on the bottom of the environment with calculated flow rates to effectively replace the old environment without creating unnecessary currents in the system.

These chambers include stringent airborne molecular contam-ination filtration for ammonia, amines, and sulfur dioxide, as well as other acid and base and sulfur dioxide controlled to the parts per trillion (ppt) levels to protect the lens systems from unacceptable rates of contamination growth. Because all materials outgas to some degree, the chambers are continuously flushed with a fresh supply of ultra-pure inert gas to eliminate even low levels of outgassed contamination.

To purge or not to purge

“Both purification and purge technologies are being used to prevent haze and crystal growth,” Niebeling says. To that end, Entegris recently launched the Clarilite Certified brand system, which reduces the need for frequent reticle cleaning by providing a continuous cleansing environment for the reticle using chemically purified gas. The system includes products and services for work-flow analysis, engineering, gas microcontamination, microenvironment control, and testing to prevent reticle haze.

However, because enclosed purge gas systems are an expensive solution, it doesn’t make sense to enclose every process step, Niebeling says. “Purging everything doesn’t pay off, but selected use does. The six million dollar question is which steps to purge to see that payoff.”

Unfortunately, every fab owner has to make that discovery on their own because every wafer process environment is different and the most valuable information is typically proprietary.

“It depends on the process, the device, and the layout of the operation,” Niebeling says, adding that the most likely steps where purging would be appropriate are those in which there is the potential for unintentional oxide growth, steps with electrical properties, and processes that involved layering in which molecular deposit can affect adhesion. “We advocate a system approach. Purging alone won’t solve all your problems. It has to be part of a larger system that includes good materials, proper sealing, and appropriate filters and monitoring. The ability to purge just adds to that system, making it even more effective.”

Hartzell points out that one of the ways to determine which steps require purging is to identify those areas that can or can’t live with swings in temperature and humidity. “If they can’t handle changes of less than a degree, you may need to isolate them or you’ll see yield problems due to corrosion or static.”

It is also a way to begin energy reduction strategies. “The semiconductor industry sucks a lot of energy out of the world,” Hartzell says. “We have to pay attention to the environment and how much energy and water we use if we want to continue to develop this field.”

In response to that, the ITRS is currently exploring the acceptable ranges for temperature and humidity in the wafer fab in an effort to address soaring fuel costs. “It’s the first step toward identifying ways to save energy in the fab. If we can focus strict energy and humidity control down to the tool environment, we can have looser specs for temperature and humidity in the fab,” Hartzell says. “ITRS is very focused on making sure the industry becomes more energy efficient. Our goal is to help with the energy and water situations while still providing high yield and a reliable path to successful development.”

Companies such as Lighthouse Worldwide Solutions, a supplier of contamination monitoring systems in Fremont, CA, now offer low-cost temperature and relative humidity sensors as part of an integrated solution for such monitoring needs. The Lighthouse tool can be used in or near process equipment to provide a real-time view of environmental conditions in the vicinity of the product.

Keeping watch

Once the contamination control system is in place, whether it includes purge chambers, minienvironments, or open ballrooms, continuous monitoring of the environment is a necessary step to maintaining a leaner, more effective fab and is a fundamental part of next-generation lithography subsystems. Continuous monitoring of the tool subsystem environment and the inert gas inputs to the tool is required for damage limitation. In 157 nm lithography systems, verification of input gases to the tool from the fab is critical in order to ensure that the supply is maintained within specs. For extreme UV (EUV) lithography systems, monitoring of moisture and hydrocarbons in the vacuum tool environment is also essential.

One promising development in monitoring molecular contamination is the use of surface acoustic wave (SAW) technology, says Hartzell. This technology uses a high-frequency, temperature-controlled SAW sensor to detect miniscule changes in mass on critical surfaces caused by interaction of organic and inorganic contaminants. “It shows in real time if something has deposited on a surface that you don’t want there,” she says.

Ion mobility spectroscopy (IMS) of sub-ppb levels of amines and ammonia, and photo acoustic spectroscopy (PAS) to quantify organics such as methane and siloxane, are also useful monitoring techniques. Particle Measuring Systems offers the AiM-200, a monitor using a SAW sensor to detect surface molecular contamination as ng/cm2 output, which can be correlated to sub-ppb levels. The company also has a Molecular Contamination brand ion mobility spectrometer for ppb level monitoring of acids and bases. This offers the advantage of being able to see the net effect of complex air chemistries, environmental conditions, and the chemical/physical nature of the surface and provides data that complements traditional test wafer monitoring.

However, these tools can be financially out of reach for some fabs, notes Hartzell. “The need for more low-cost in situ monitoring techniques to control specific areas in the fab is apparent.”

One lower-cost alternative is grab sampling, which provides an environmental snapshot of the fab, Camenzind notes. This method of testing is highly selective and provides a detailed identification of each chemical detected. However, it doesn’t capture random events and AMC excursions such as chemical spills, and it takes several days to get test results. The best combination for testing, in his opinion, is more expensive online monitoring for the most critical processes and grab sampling when needed to more rigorously identify contamination periodically or during upsets.

“In the end, it’s an industry driven by dollars, yen, euros, yuan, or won,” says Camenzind. “You want high, predictable yields but you don’t want to waste money. To achieve that, you have to identify what affects each process step -not the whole fab-and take reasonable precautions against the most probable upsets.”


SEMATECH explores wafer cleaning at 45 nm and beyond

SEMATECH is exploring potential solutions for preparing wafers for manufacturing at and beyond the 45 nm technology generation. Technologists at SEMATECH’s 2007 Surface Preparation and Cleaning Conference in April reported several techniques for non-damaging particle removal from wafer surfaces, along with multiple methods for removing photoresist with minimal silicon and oxide loss.

“The 45 nm generation is coming up fast-and some chip-makers are there already-and many of the manufacturing issues are connected to surface preparation and cleaning,” said SEMATECH’s conference chair, Joel Barnett. “The conference made it clear that many of our chemistries and approaches will have to change, but that plenty of potential solutions are being considered for 45 nm and beyond.”

Some potential solutions included:

  • Shock tube-enhanced laser-induced plasma (LIP) shock waves for sub-50 nm nanoparticle removal, from Clarkson University. This approach confines LIP beams to specially engineered “shock tubes” to increase the cleaning power of shock waves.
  • Plasma-assisted cleaning by electrostatics (PACE), offered by the University of Illinois at Urbana-Champaign. This technology utilizes broad-area plasma to provide a negative charge to contamination, allowing it to be repelled electrostatically.
  • An ionized molecular-activated coherent solution, proposed by Nano Green Technology, Inc. This method uses a charged solution of ammonia in water to form clusters that attract particles at the molecular level without damaging the wafer surface.
  • Parametric nanoscale cleaning from Lancetta, Inc. The company suggested a technology that removes particles by forming nanoscale bubbles to absorb the contaminants.

Solutions for photoresist issues included photoreactive cleaning from UVTech Systems; a CO2 cryogenic press and non-oxidizing chemistry from DuPont Electronic Technologies, EKC Technology, and BOC Eco-Snow Systems; and methodologies for all-wet chemistries from FSI International and SEZ Group.

Earlier in the conference, keynote speaker Jadgish Prasad of AMI Semiconductor urged engineers to consider the requirements of surface cleaning when designing future generations of microchip circuits. Design dominates how wet processing is done, and processing limitations in turn influence the design process, he said.

Reflecting a chip-maker’s perspective, Prasad emphasized the critical influence of surface preparation on yield and reliability. “Sixty percent of fab-related (yield) problems are related to cleans, and another 12 percent to etching steps,” he said. Prasad predicted that manufacturers will need to adopt new etch chemistries and cleaning regimens for the 45 nm generation and beyond.