Understanding the Value of Modular Cleanrooms

Understanding the Value of Modular Cleanrooms

At Angstrom Technology, we like to take a step back every once in a while, taking the time to acknowledge and appreciate the impact of our work in various industries. It helps us put our work into perspective, and it motivates us to deliver excellence each and every day.

As we’ve reflected throughout the past years, we’ve always been astonished at how much innovation happens within modular cleanrooms. These quickly built, easily modified, heavily treated chambers truly make groundbreaking work possible. As a resource that helps scientists, and engineers test, manufacture, and package products safely, cleanrooms bring tremendous value not only to the workforce, but to society as a whole. 

In this article, we’ll explore some amazing ways that various industries have used modular cleanroom technology to trailblaze a path of innovation.

The Value Modular Cleanrooms Bring to Various Industrial Applications

Modular cleanrooms have proven themselves to be beneficial for a number of applications, in a number of industries. Some of history’s most important inventions required cleanrooms’ quality control, and some of the future’s best and brightest innovations are being tested in them today. Below, let’s discuss some common industries that use cleanrooms, and what important things they’re using them for. 

Aerospace

Aerospace cleanrooms are crucial for the development of aircraft and spacecraft hardware, fine electronics, engine components, and more. In order to manufacture, assemble, and test those components, the aerospace industry needs a high level of control over the cleanroom environment — usually meeting an ISO Class 7 requirement, at minimum.

Each day, aerospace engineers are working hard to develop technologies that help us continue our journey of exploring the unknown. Modular cleanrooms give them the space they need to do that revolutionary work. 

Semiconductor

Semiconductor cleanrooms prevent particles from contaminating certain parts of nanotechnology — like semiconductors and microchips — that allow us to operate phones and computers more safely and efficiently. When even the smallest bit of contamination can lead to serious product issues and failures, a stringent modular cleanroom environment of ISO Class 5 or lower is necessary. 

Our world is reliant on constant technological innovations in order to stay connected, do business, and maintain a quality lifestyle. Modular cleanrooms will always provide a space to make those technological advances happen.

University Labs and Research Facilities

University labs and research facilities encompass a variety of applications, from medical research, to forensic science, to hazardous chemicals. Additionally, the university setting requires that spaces are able to be reassigned and restructured as student, research, and funding needs change throughout the years. Therefore, the versatility of quickly built, easily modified modular cleanrooms is extremely valuable here. 

Universities host some of the most advanced, highly recognized research facilities. Students and faculty are working with state-of-the-art technology to solve some of their industry’s most perplexing problems. A modular cleanroom can provide a controlled environment to foster that learning, no matter what the specific application may be. 

Military 

In regards to the military, weapons manufacturing is a critical component in upholding national security and protecting American citizens. Due to the deadly nature of the products and volatile compounds used in this industry, a controlled cleanroom environment is crucial in maintaining the safety of information, products, and personnel. 

Weapons manufacturing is, and always will be, dangerous. However, it plays a key role in protecting our nation’s infrastructure from devastating threats. Modular cleanrooms can help lessen the risk and bolster the production. 

Angstrom Technology can design a modular cleanroom to meet all your requirements and design considerations. If you’re interested in designing and installing one for your facility, speak with one of our design engineers to get started.

cleanroom-classification-quiz-cta
How to Set Up a Semiconductor Manufacturing Cleanroom

How to Set Up a Semiconductor Manufacturing Cleanroom

Semiconductors are extremely sensitive materials. So without a controlled cleanroom to manufacture the chips in, you risk contamination that could lead to various production issues and product failures. 

If your facility manufactures semiconductor chips for computerized devices of any type, size, or application, you’ll need a semiconductor manufacturing cleanroom. Let’s take a look at what components and considerations go into designing one. 

Where to Start: Understanding the Requirements of a Semiconductor Cleanroom

Even the slightest bit of contamination or settling of particulate produce can ruin semiconductor production and performance, sometimes leading to disastrous consequences. Therefore, it’s important to understand the strict cleanliness standards that semiconductor cleanrooms must abide by. 

Semiconductor Cleanroom Classifications

Even the slightest bit of contamination or settling of airborne particles can compromise semiconductor manufacturing efforts — leading to costly product defects. So before you get started designing your semiconductor manufacturing cleanroom, you should gain a thorough understanding of the threats they’re faced with and the cleanliness standards they must abide by. 

Semiconductor Manufacturing Threats

When working in a semiconductor manufacturing cleanroom, operators face a number of challenges regarding detailed processes and contamination control. In fact, human workers themselves are often the main source of contamination during the semiconductor manufacturing process. Aside from particulate matter from their bodies and clothing, they can create unwanted electro-static discharge (ESD) that can ruin electronic circuits in the material. 

Other than that, there are a number of additional environmental threats that can disrupt the semiconductor manufacturing process

  • Static
  • Humidity
  • Airborne particles
  • Power glitches
  • Pressure malfunctions
  • Equipment outgassing
  • Dropped equipment, tools, and parts

Yes — that’s a lot to keep in mind! But semiconductors are so fragile that even the tiniest speck of dust can destroy them.

Fortunately, a reliable, controlled cleanroom can do most of the work for you. When designed, built, and installed properly, your semiconductor manufacturing cleanroom can maintain the level of environmental control you need to optimize productivity and profitability. 

 

angstrom-perfect-semi-conductor-setup-cta

When You’re Ready: 4 Steps to Designing a Semiconductor Manufacturing Cleanroom

Now that you’re aware of the threats your semiconductor manufacturing cleanroom faces and the standards it needs to meet to prevent them, it’s time to start on design. Below we’ve outlined four considerations you’ll want to keep in mind during the design process. 

1. Start with Cleanroom Airflow & Air Filtration 

Airflow and air filtration are two of the most important aspects of great semiconductor manufacturing cleanroom design. They both determine how many airborne particles travel into your cleanroom and how they’re prevented from building up on equipment and materials. Let’s break them down one by one. 

Cleanroom Airflow

ISO 14644-4 describes recommended cleanroom airflow patterns at various classification levels. The most popular (and widely recommended) airflow pattern is unidirectional, or laminar. It involves air blown at a constant speed in a straight and unimpeded path. The air is pushed through a filter (usually in the cleanroom ceiling) and then directed down toward the floor. To reduce turbulence, some semiconductor cleanrooms have raised flooring that use perforated tiles that allow air to flow through holes where it can be retreated and filtered before entering the cleanroom again. 

Cleanroom Air Filtration

Cleanroom air filtration is all about how many airborne particles, and of which sizes, are permitted within a cleanroom. Regulations for this are documented in the ISO 14644-1 classification system. 

Airborne particles are controlled with specialized air filtration systems, such as HEPA and ULPA filters. You can learn more about these systems and how they work on our air filtration page

2. Consider Cleanroom Furniture and Machinery Placement

Semiconductor manufacturing requires various types of furniture, machinery, and equipment. It’s a good idea to map out where these items will be placed in order to produce the most efficient airflow patterns. 

One of the best recommendations for semiconductor manufacturing cleanroom design is to place large furniture, machinery, and equipment along the outer walls. This helps decrease the chance of those big objects obstructing the main airflow. 

Many cleanrooms are also designed with wire racks and shelves instead of regular shelving. This eliminates a portion of flat surfaces that contaminants can build up on. 

3. Implement Anti-Static Protection

Electro-static discharge (ESD) can ruin semiconductors’ conductive properties. To prevent ESD, your semiconductor manufacturing cleanroom must take preventative measures. Cleanroom wall panels, flooring, furniture, and more should be manufactured with static dissipative materials. You may also include various ESD-free products like clothing, tools, and cleaning materials. 

4. Plan For Daily Operations

In order to keep production moving and meet consumer demands, your semiconductor manufacturing cleanroom will likely be used daily. It’s important to design the cleanroom in a way that fits your operational plan. Make sure to note the following:

  • How your operators enter and exit the cleanroom
  • What ESD tests, gowning regimens, airlock rooms, and air showers your operators need to pass through before entry
  • How your operators move from task to task within the cleanroom
  • How often your operators need to clean the cleanroom, and what that process looks like

This information will help ensure your cleanroom is designed to maximize efficiency and cleanliness — which leads to better production quality, safety, and profitability. 

Design a Semiconductor Manufacturing Cleanroom with Angstrom Technology

Need help getting started on your semiconductor manufacturing cleanroom design? Let the experts at Angstrom Technology help. Our design team can help you make the tough choices and ensure you get the robust solution that’s perfect for your application. 

Request a semiconductor manufacturing cleanroom quote today, or contact us for more information. 

 

cleanroom-classification-quiz-cta
Medical Cleanroom Technology that Aids Surface Sterilization

Medical Cleanroom Technology that Aids Surface Sterilization

In order to keep operators and consumers safe, medical cleanrooms have some of the most stringent cleanliness requirements. Depending on whether they’re used for medical research, medical device, or pharmaceutical applications, their ISO standards can range from ISO Class 4-7.  

All that being said, if your facility hosts one or more medical cleanrooms, you may also want to invest in some innovative technologies to ensure consistently sterilized air and surfaces. Below, we’ll explore some of the new medical cleanroom technology on the market, including various portable HEPA filtration systems and peroxide sanitizing solutions. 

Portable HEPA Filtration Systems with UV-C Light Integration

While your cleanroom may already host a number of HEPA filters, some of the newest trends in medical cleanroom technology deem portable HEPA filters a rewarding investment. New portable HEPA filters can be mobile, ceiling mounted, or standalone, and they usually contain a UV-C light integrated for extra cleansing power. This way, you’re able to sterilize any specific area or surface more quickly and effectively than ever before. 

How Do HEPA Filters with UV-C Light Integration Work?

HEPA filters are known for effectively capturing microscopic viruses and bacteria with ease. Generally, airborne viruses are moved through the air via particles with a diameter between 10-100 µm. HEPA filters are capable of capturing large infectious loads of particles that are responsible for virus transmission and exponentially reducing them. 

HEPA filters can remove many of the common human pathogens from air circulation, including (but not limited to) the following:

  • Escherichia coli: Gastrointestinal infections
  • Aspergillus brasiliensis: Sinus infections
  • Mycoplasma pneumoniae: Pneumonia
  • Haemophilus influenzae: Meningitis
  • Mycobacterium Tuberculosis: Tuberculosis

When HEPA filters are combined with UV-C light technology, they can inactivate airborne-mediated microbial disease and microbial resistant bacteria even faster. UV-C lights and lamps are extremely effective, even against some of the most contagious airborne diseases. And while HEPA filters primarily cleanse the air, UV-C lights help sterilize water, hard surfaces, and nonporous objects as well. 

Portable HEPA Filtration System Features and Accessories

Along with your portable HEPA filtration system, you’re able to add on a variety of optional features and accessories for advanced performance, including:

  • Portable UV torches – Portable UV disinfection torches are about 5 feet tall, and designed to sterilize objects and tools within a medical cleanroom. They stand on their own, include 8 UV-C bulbs, and are built with an open center that allows for comprehensive sterilization within a 10-foot radius. 
  • Handheld UV light wands – Handheld UV light wands work similarly to portable UV torches, but are even more mobile. They have a lightweight, ergonomic design that is especially helpful in surface sanitation, and cleanroom inspection procedures. 

Dry Hydrogen Peroxide

Dry Hydrogen Peroxide (DHP™) is the true gas form of hydrogen peroxide, and it attacks microbes like viruses, bacteria, and mold before they can be damaging, both in the air and on surfaces. Developed by Synexis, this technology is designed to flow freely and constantly throughout your controlled space to effectively eliminate pathogens — without any reliance on air exchange rates. It works by taking the oxygen and humidity naturally present in your environment, then breaking them down in the Synexis device through a photocatalytic reaction (chemical reaction involving the absorption of light). Those molecules are then put together again, but as DHP™.

Not only is DHP™ cool and effective technology, but it’s also completely safe — falling far below safety limits for human exposure established by OSHA and meeting UL2998 certification requirements for zero ozone emissions. You can learn more about how DHP™ works and benefits various applications here

If you’re looking to upgrade your medical cleanroom technology to include some of the newest innovations, contact Angstrom Technology! Our cleanroom design experts can make sure your facility is outfitted with the best gadgets and gear to protect your work and workers.

cleanroom-classification-quiz-cta
Cleanroom Classification FAQs

Cleanroom Classification FAQs

Cleanroom classification is often one of the most confusing parts of designing and building a cleanroom. However, it’s also one of the most essential parts, so it’s important that you understand all the relevant information.  If you’re installing a cleanroom for the first time, you probably understand that every type of cleanroom requires a different classification, but you’re bound to have a number of other questions — and that’s okay! We’re here to help. Below, we’ll provide answers to some of the most common cleanroom classification questions we receive.

1. What are cleanroom classifications?

Cleanroom classifications regulate a cleanroom’s degree of cleanliness. They’re defined by the allowed amount of contamination, by particle count and size, as well as the air change rates necessary to maintain that.  There are a variety of classification types that regulate cleanroom cleanliness, but the main system was developed by the International Standards Organization (ISO). ISO classifications apply to all cleanroom industries and applications, and range from Class 1 (most clean) to Class 9 (least clean, regular room air). 

2. What cleanroom classification do I need?

It depends on your industry and application. The requirements will vary depending on the size of particles that need to be filtered, the sources of contamination present, and the recommended air change rates. If your industry is regulated by the government, you can check applicable regulations to see what cleanroom classification is required. If you work in a sector that isn’t regulated by the government and that doesn’t have an industry default, you’ll need to determine the appropriate classification for yourself, based on your application’s needs.  Below, we’ll explore recommended cleanroom classifications for a few popular industries. For a full list of industries and their cleanrooms classifications, visit our cleanroom industries page

What cleanroom classification is best for aerospace applications?

Aerospace applications require control over mechanical, thermal, chemical, and electrical properties within the cleanroom. In most cases, their cleanrooms need to meet at least a Class 7 ISO classification. However, in highly sensitive applications like spacecraft hardware, fine electronic, and optical device development, a more stringent classification is necessary.

What cleanroom classification is best for manufacturing applications?

There are various types of manufacturing processes, all with different needs in terms of humidity, contamination, pressure, and temperature control. However, most manufacturing cleanrooms tend to be required to meet ISO Classes 7 or 8. 

What cleanroom classification is best for medical applications? 

There are a few sub-categories that fall under the broad category of medical cleanrooms, including medical research, medical device, and pharmaceutical cleanrooms. All of these cleanrooms have some of the most stringent classifications in order to protect the safety of operators and consumers. 

  • Medical research: ISO Class 5-7
  • Medical device: ISO Class 5-8
  • Pharmaceutical: ISO Class 5

What cleanroom classification is best for semiconductor applications?

Contamination is a large source of production issues and product failures in semiconductors and microelectronics, so it’s critical that the cleanrooms they’re manufactured and packaged in are filtered appropriately. In most cases, semiconductor cleanrooms will hold ISO Class 4-6 requirements. 

3. How often should I test my cleanroom to see if it’s meeting classification requirements?

ISO requires that air pressure difference and airflow be tested every 12 months for all classifications. For ISO Classes 6-9, particle tests must also be performed every 12 months, but for ISO Classes 1-5, those particle tests must be performed every six months.  The following tests are recommended for all ISO Classes, every 24 months:

  • Installed filter leakage
  • Containment filter leakage
  • Recovery
  • Airflow visualization

4. How often do I need to have my cleanroom inspected?

That depends on your cleanroom classification. The more stringent the classification, the more regular the inspections. Inspections may coincide with compliance testing, so they could occur every 6-12 months, depending on your specific requirements. 

5. How does cleanroom classification affect my budget?

In general, the more stringent your cleanroom classification, the greater the cost. Strict classifications require more air, energy, advanced technology, and equipment, so their prices reflect that. For a more detailed breakdown of the costs, you can check out our blog, “How Does Cleanroom Classification Affect Your Cleanroom Budget?”

6. Can I redesign my cleanroom to fit a different classification?

Yes. Every facility’s needs change over time. A cleanroom from Angstrom Technology can change right along with them. All of our cleanrooms are “backward compatible,” meaning their size can expand or decrease and their fan filter units can be added or removed to keep up with any changes in cleanroom classification requirements.  Have any questions about your cleanroom classification and how to reach it? Contact the experts at Angstrom Technology! We’re happy to walk through your specific requirements and help design and build the best cleanroom for your facility and application.