NQ Industries provides clear terms and clean air for ARP ESSER recipients

The American Rescue Plan (ARP) Act was signed into law on March 11, 2021. The $1.9 trillion package includes $122 billion for the ARP Elementary and Secondary School Emergency Relief (ARP ESSER) to assist State educational agencies and school districts reopen and sustain the safe operation of schools and address the impact of the coronavirus pandemic on the nation’s students.

While about 20% of the funds must go for efforts to reduce “learning loss,” an unspecified amount can be devoted to mitigating virus transmission, improving environmental health, meeting the Centers for Disease Control and Prevention (CDC) health guidelines and protocols. NQ is rising to the challenge, using its three decades of experience to help learning institutions make the most efficient use of the funds while creating the most effective solution to indoor air quality improvement.

“Our academic leaders are challenged with allocating funds for essential needs, which first and foremost is providing a healthy environment for students and staff,” states NQ President William Carey. “We are helping educators avoid investing in ineffective systems and guiding them to long-term solutions that are easy to implement and proven to deliver pure, safe indoor air for decades to come.”

For over 29 years, NQ has been guiding Elementary and Secondary Schools throughout the United States to help improve indoor air quality (IAQ) and create healthier learning environments.

NQ’s Single Pass Kill® systems — proven to trap and kill airborne pathogens in a single pass while exceeding CDC, EPA, and ASHRAE guidelines — protect both the health and investment of institutions. NQ systems provide long-term solutions and save schools from the costs of retrofitting current HVAC systems. The NQ systems only need to be plugged in and start to work instantly.

Richmond Hill, Trinity Day, and The Children’s Center of Hamden are some of the many institutions choosing to invest in NQ medical-grade systems to help protect their spaces against viruses, bacteria, and molds that contribute to short and long-term health problems for students and staff.

As Sarah Lockery, LMFT, Chief Development and Engagement Officer of The Children’s Center, states, “The air is cleaner and healthier at The Children’s Center of Hamden thanks to NQ Industries air purification systems.”

The expert team at NQ is helping lead educators avoid investing in false claims and sub-par systems that are new-to-market and ineffective against COVID-19. To find out how your school officials can receive NQ ARP ESSER guidance from an NQ Air Purification Specialist, contact Lionel Reid via email at LReid@nqinc.com or call 860-990-3591.

About NQ Industries
Bill Carey and his NQ team began developing air purification systems designed to support airborne infection control for Tuberculosis isolation rooms in 1992. Over two decades later, the same pioneering technologies, combining HEPA and Ultraviolet (UVGI), are clinically tested and globally proven to kill airborne pathogens, including COVID-19, in a single pass. NQ is proud to be the industry leader providing solutions for pure, safe air to learning institutions, government branches, and commercial customers around the world.

To learn more, visit NQinc.com.

NQ Industries Supports The Children’s Center of Hamden With Cleaner and Healthier Air

Founded in 1833, The Children’s Center of Hamden is Connecticut’s oldest childcaring agency. Helping children and families for close to a century, The Children’s Center is a private, nonprofit behavioral health organization dedicated to assisting individuals of all cultural backgrounds to achieve their highest level of functioning through quality treatment, education, and care. Providing hope to youth who struggle with psychological or social problems, physical or sexual abuse, learning disabilities, substance abuse, and family trauma has been the mission of the Children’s Center.

The center’s treatment programs are licensed by the State of Connecticut, and Whitney Hall School is accredited by the Connecticut State Department of Education. With a Gold Seal accreditation from The Joint Commission for Behavioral Health Care Services, the center continues to support mending the hearts and minds of the community they serve with a wide array of services as unique as the individuals they serve.

Consistent with the center’s efforts to provide equitable health for all served, it is a high priority for the multi-service agency to not only ensure the center is a welcoming place for all but a healthy one as well. So, in seeking out the best solution to provide cleaner indoor air, The Children’s Center partnered with NQ Industries.

With the understanding of the comparative risk studies performed by EPA’s Science Advisory Board (SAB) consistently ranking indoor air pollution among the top five environmental risks to public health and also stop the spread of the COVID-19 virus, maintaining good IAQ (Indoor Air Quality) is an essential need of the center. To help preserve The Children Center’s healthy indoor environment, NQ Industries, located on Sherman Avenue in Hamden, CT, donated air purification units to match those purchased by the Center.

Combining innovative technologies and the ancient practices of “clean rooms” for healing, Bill Carey and his NQ team began developing air purification systems designed to support airborne infection control for Tuberculosis isolation rooms in 1993. Now, 20 plus years later, the same pioneering technologies, combining HEPA and Ultraviolet (UVGI), are clinically tested and globally proven to kill airborne pathogens, including COVID-19, and provide pure, safe air for medical institutions, military and commercial applications around the world.

“Whether it’s patients stricken with TB or public health concerns about the spread of COVID, our mission is to help people, and that is what our systems do — actually kill every airborne infection in the room – if it’s a pathogen, it is not making it through our machine period,” states Bill Carey, the president of NQ.

Driven by innovation and an unwavering commitment to provide highly efficient, unsurpassed quality and safe maintenance for easy to use, quickly deployable, and economically viable systems, NQ wanted to make sure The Children’s Center was outfitted with air purifiers. “The work the Children’s Center of Hamden does is important to us as a company, states Elizabeth Carey, NQ Industries VP of Operations, “because children are our future.”

Since adding the air purifiers, “the air is cleaner and healthier at The Children’s Center of Hamden thanks to NQ Industries air purification systems,” affirms Sarah Lockery, LMFT, Chief Development and Engagement Officer of The Children’s Center.

That’s because, through accurate assessment of required Air Changes per Hour, NQ Air Purification Units solve the issues of inadequate ventilation and internal and external contamination with 99.9% removal of airborne contaminants. The systems have helped thousands of worldwide organizations eradicate airborne pathogens, including MRSA, SARS, Tuberculosis, Aspergillus, and now Coronavirus (COVID-19).

Derived from the phrase “Natures Quarters,” NQ has spent two decades delivering on its promise to create safe, healthy indoor environments by developing peerless air purification solutions that protect all communities and help provide peace of mind.

To find out more about how NQ Industries can help your organization actualize healthy indoor environments visit, https://nqinc.com/contact/.

2 Decades of NQ Air Purification Facts and Figures At-A-Glance

In 1992, the NQ team began developing air purification systems designed to support airborne infection control for Tuberculosis isolation rooms. Now 20+ years later, the same pioneering technologies, combining HEPA and Ultraviolet (UVGI), are clinically tested and globally proven to kill airborne pathogens, including COVID-19.

This infographic showcases some of the many stats that have made us the proven leader in improving indoor air quality (IAQ) and providing pure, safe air for medical institutions, military and commercial applications around the world.

For more information on how NQ Air Purification Solutions can help create a healthier indoor environment for your organization, contact us today.

5 Vital Health Benefits of Ultra Violet Germicidal Irradiation (UVGI)

Strong evidence exists for the airborne transport and transmission of SARS-VoV-2 coronavirus (COVID19) (CDC 2020, CDC2020a). Various agencies have issued statements in regard to airborne SARS-C0V-2 coronavirus including ASHRAE and CDC who recommend the use of UVGI as a supplement to help inactivate (kill) SARS-CoV-2 and reduce the overall viral dose to indoor occupants.

All HAI pathogens being identified as being transmitted by airborne route in indoor air environments, most of these pathogens are increasingly becoming resistant to antibiotics, antifungal agents and vaccines. As vaccines, antibiotics and antifungal agents lose their effectiveness against these pathogens, air cleaning technologies such as UVGI may be the only effective, potent recourse of protecting patients and healthcare workers in indoor medical and commercial environments.

Applications of UVGI systems in hospitals, schools and commercial buildings have often achieved high levels of success when systems are properly designed and installed.

Here are 5 compelling reasons why UVGI is a vital part of an effective air purification system:

Safe, proven, effective. 100 year+ use in the medical air and commercial water industry

Produces no ill effects or by-products (properly designed and constructed).
No harmful gasses, no heat gain, in properly designed systems.

Long lasting (10,000 hours of operation)

Will kill all known airborne and surface pathogens.

Uses little energy to produce desired effects

Why do NQ Air Purification Systems combine Ultraviolet Germicidal Irradiation + High Efficiency 99.99% HEPA? UVC radiation at 254nm has an intense germicidal effect. UVGI alters the pathogen’s DNA/RNA, inhibiting its ability to replicate. Micro-organisms, such as viruses, bacteria, fungi and yeasts are effectively deactivated without the addition of chemicals within seconds.

To learn more about how NQ Air Purifications Solutions can help create a healthier indoor environment for your organization, contact us today.

 

 

 

 

 

 

 

Proposed Standards and Guidelines for UVGI Air Disinfection

INTRODUCTION

In spite of widespread use of ultraviolet germicidal irradiation (UVGI) for air disinfection applications, there are currently no consensus standards for the design, application, or testing of UVGI air disinfection systems. Several agencies and organizations are in a position to develop such documents, including the Centers for Disease Control (CDC), American Society of Heating, Refrigerating and Air- Conditioning Engineers (ASHRAE), American National Standards Institute (ANSI), American Society for Testing and Materials (ASTM), National Environmental Balancing Bureau (NEBB), and others, but none of these groups currently have plans to do so. As a first step in the direction of standards, guidelines are needed that address specifics of the design, operation, and testing of UVGI components and systems for commercial and health care applications. Such documents will provide a basis for the development of consensus standards analogous to ASHRAE Standard 52.2- 1999 for rating filters and ASHRAE 90.1 for whole-building energy efficiency (ASHRAE 1999, 2001). This article outlines requirements for the guidelines and standards needed to ensure successful UVGI applications and reviews the availability of data for their development.

EXISTING GUIDELINES

A number of currently available documents provide information on aspects of UVGI system design, installation, and testing, but no comprehensive standard exists that can ensure that installed UVGI systems are safe and effective. Many components of a potential standard exist in piecemeal fashion in these documents. Guidelines are available from sources such as the Illumination Engineering Society of North America (IESNA) that address the design, testing and rating of UV lamps (IESNA, 2000; CIE, 2003). Electrical safety of UVGI components can be certified by testing laboratories such as UL and ETL in order to ensure they are suitable for operation inside ducts, plenums, or other locations. Safety and health hazards from UV exposure have been addressed by various agencies (NIOSH 1972; ACGIH 1991; AIHA 2001; IRPA 1985; NEHC 1992). Guidelines from the Centers for Disease Control (CDC) have addressed the use of UVGI for tuberculosis control and infection control but provide no specific design guidance (CDC 1994, 2003). Guidelines from the General Services Administration provide recommendations for using UVGI to control mold in mechanical HVAC systems, but without detailed technical information (GSA, 2003). The ASHRAE HVAC Design Manual for Hospitals and Clinics addresses the capabilities of UVGI but includes no specific guidelines (ASHRAE, 2003). The use of air treatment to mitigate bioterrorist threats has been addressed in several documents (NIOSH,

2002 & 2003, FEMA 2003, 2003a, & 2003b). Numerous books, catalogs, and publications have provided piecemeal information on the design and performance capabilities of UVGI in applications, but as yet no definitive guideline or standard has been proposed that would provide accurate and reliable design information (Kowalski and Bahnfleth, 2000a,b; Kowalski, et al., 2000; Philips 1985; VanOsdell and Foarde, 2002, Bolton, 2001).

UVGI System Applications

UVGI systems find increasing varieties of applications as a result of both real and potential airborne disease threats, including emerging diseases like SARS virus, increased resistance of some species such as Staphylococcus aureus and Mycobacterium tuberculosis to antibiotics, the continued threat of species-jumping diseases like avian flu, the ever-present problem of indoor mold growth coupled with increased incidence of asthma and allergies, the recognition of airborne vectors in food pathogens, and the threat of bioterrorism.

Table 1 provides a summary of where UVGI systems are applied today and what types of systems are typically used. The mold growth control systems referred to are often used for controlling microbial growth on cooling coils and air handling unit components.

TYPES OF UVGI SYSTEMS

The various types of UVGI systems may have different design and testing requirements. Figure 1 shows a breakdown of the most common types of UVGI systems used today. Each of these systems will of necessity require some degree of separate consideration in terms of performance and testing standards.

In addition to the types of UVGI systems, the variety of UVGI applications necessitates some variation in performance requirements. UVGI systems installed in commercial office buildings for biodefense will probably have different requirements than those installed in hospitals for nosocomial infection control, or those installed in homes for allergen control. Some systems may serve a dual purpose, disinfecting both the air stream and the internal Air Handling Unit (AHU) surfaces, as shown in Figure 2.

LABORATORY TEST RESULTS

In support of a UVGI standard, it will be necessary to assemble or develop reliable data on the performance of UVGI against microorganisms. Although there have been over a hundred laboratory experiments on the effectiveness of UVGI against viruses, bacteria, and fungi, most of these were performed in water or on surfaces. Tests of airborne disinfection rates suffer from experimental problems, including unrealistic operating conditions, heavy dependence on the test apparatus used, uncontrolled conditions, and sometimes arbitrary interpretation of results. The lack of standardization in laboratory tests on UVGI system has sometimes resulted in contradictory results. It will be necessary to establish laboratory testing guidelines to ensure results that are reproducible and reflect real world conditions. Perhaps a standard test apparatus will have to be designed that operates under controlled air velocity, air temperature, and relative humidity, and that can be used to give accurate, reproducible results for the UV rate constants of microorganisms. Such testing can be performed on the dozens of pathogens and allergens of current interest in indoor air quality and health care applications. The ultimate goal will be the development of a reliable database of airborne and surface UVGI rate constants or dosages necessary for disinfection and/or sterilization.

PERFORMANCE CRITERIA

It is essential to define an acceptable range of performance for UVGI systems for any given application. Air filters are rated by various means, including such as the “minimum efficiency reporting value” (MERV) defined by ASHRAE Standard 52.2 (ASHRAE 1999). The concept of a similar rating system for UVGI air disinfection systems called a UVGI Rating Value (URV) has been previously proposed (Kowalski and Dunn, 2002, Kowalski, 2003). The URV for any given UVGI system is based on the UV dose produced, which is defined as the product of exposure time and irradiance and has units of μJ/cm2 (or μW-s/cm2). Table 2 shows the proposed breakdown of UV doses used to define the URV. This breakdown is based on a general review of current installed UVGI systems and is open to revision if necessary. Table 2 also shows a sample of inactivation rates that would be obtained by the indicated URV. Any air disinfection system can be categorized by a URV, and, in fact, when the URV is matched to the MERV rating for the associated filter, a combined MERV/URV system will produce roughly equivalent removal rates for the entire array of pathogens and allergens.

AIR FILTRATION

UVGI air disinfection systems must include air filtration to protect the lamp from dust. Furthermore, fungal and bacterial spores that tend to be resistant to UVGI are often highly filterable and the combination of filtration and UVGI can effectively remove a broad range of airborne microorganisms. Filter specifications therefore form an integral part of the design of any UVGI system.

Fortunately, air filtration guidelines are already in existence and these can simply be referred to in the proposed standard. ANSI/ASHRAE Standard 52.2-1999 addresses methods for testing air-cleaning devices for removal efficiency by particle size, and provides the Minimum Efficiency Reporting Value (MERV) by which production filters are rated.

It is necessary to verify that filters are installed properly and do not leak or bypass air. A small amount of bypass air can result in a great reduction in filter efficiency. At a minimum, filters should be inspected to verify that all seals are tight and no holes or damage exist in the filter media. The next level of verification of filter performance is an in-place filter test. However, the cost of such a test may not always be justifiable, whereas the methods proposed herein for testing and commissioning the overall air treatment system will likely be sufficient to demonstrate the presence or absence of any significant filter bypass.

INSTALLATION AND MAINTENANCE REQUIREMENTS

Guidelines also need to address basic installation requirements, including safety considerations and maintenance. Placement or location of UV lamps, adherence to testing requirements for electrical components such as UL or ETL, the use of safety switches, use of reflective materials, and maintenance requirements can be consolidated from current practices. Often the manufacturers of such air cleaning equipment provide detailed guidance, but consensus minimum standards for installation should be defined to prevent misapplications and sub-standard installations. Safety requirements also impact the handling and disposal of UV lamps, especially those that contain mercury. In some applications, such as in the food industry, unbreakable lamps may be required.

TESTING AND COMMISSIONING

In addition to design and installation requirements, there is what may be the most important aspect of any UVGI application — testing and commissioning. Protocols for testing and commissioning of UVGI systems need some degree of standardization to define acceptable performance, or at least, to rate the systems on some common scale. Testing and commissioning of UVGI systems is necessary to ensure that any installed system performs as designed. Various types of tests are possible, including verification of rating or UV output, challenge testing, and air sampling of before-and-after ambient airborne concentrations of natural building microflora, as summarized in Table 3.

The techniques and test protocols for air and surface sampling of microorganisms are in common use and various guidelines are available (Aerotech 2001; Vincent 1995; Boss and Day 2001, Jensen and Schafer 1994). These methods will be adapted and standardized for the particular application of air treatment systems in buildings and air handling units.

The criteria of acceptability for air sampling before and after UVGI installation can vary from building to building. The matter is complicated by the fact that no such standards exist for indoor air. For healthy commercial buildings, an acceptable level of fungal spores might be less than 300 cfu/m , based on the authors’ review of various studies, although levels above 1000 cfu/m3 are not necessarily harmful (ASHRAE, 2003; Kowalski, 2003). Similar levels may be acceptable for airborne bacteria in occupied buildings.

The installation of a UVGI or filtration system would be expected to reduce indoor airborne levels below normal levels. Since some buildings may start with high levels and others with low levels, it is difficult to assign a specific criteria of acceptability, and it can only be advised that some significant reduction in airborne levels of both bacteria and fungi would be expected when air treatment systems are put into operation for a few days or weeks. In one hotel room, for example, the fungal spores measured an average of 300 cfu/m3 during winter when the outdoor air was about 63 cfu/m . After retrofitting a UVGI system, levels dropped to 3 about 12 cfu/m . These results are shown graphically in Figure3. Of course, seasonal conditions might produce much higher levels of spores and 300 cfu/m3 might prove to be an acceptable reduction in summer or fall.

UVGI surface disinfection systems, such as are currently used to disinfect cooling coils, duct, and filters, also need to be standardized and this could be accomplished in the same guideline. Table 4 shows the basic types of testing that could be used for surface disinfection systems. Often, a UVGI system serves the dual purpose of both air and cooling coil or filter surface disinfection and in such cases surface sampling might be used in lieu of air sampling to demonstrate the effectiveness of the UVGI system.

In the case of surface disinfection, it could be expected that all exposed surfaces would be sterilized after a few days or weeks of UV exposure, and therefore the criteria of acceptability is to have negligible or zero cfu per square inch of sampled surface area. It is often difficult to obtain a zero cfu surface sample, since even the act of sampling may introduce trace levels of bacteria or fungi, so the criteria of acceptability may have to be stated as “approximate sterility.” Sterility is a technical term, defined as six logs of reduction, which, depending on initial conditions, may or may not be possible to prove. That is, if the “before” condition shows 100,000 cfu/in . of surface and the “after” condition shows 1 cfu/in , this may not absolutely prove that sterility has been achieved but it certainly demonstrates that the system is working. Figure 4 shows one example of an air handling unit for which surface fungal spores had been measured before and after the installation of a UVGI system.

BUILDING PROTECTION FACTOR

The effectiveness of any unit, whether in-duct or stand- alone, is limited by the application in which it is placed. The performance of any air treatment system is coupled with the building or facility in which it is placed. Building volume, airflow, building air quality criteria, etc., will define the operating requirements of any air cleaning system, and if the air treatment system is not precisely sized for the application, the performance will be affected by the building characteristics. Although an installed air treatment system may have high rates of microbial removal, its true effectiveness will depend on a combination of system airflow, building volume, degree of air mixing, and other factors. It may be necessary to define an additional rating system for buildings that quantifies the degree to which each building removes airborne pathogens and allergens. Currently, buildings can be classified as normal, healthy, sick, or immune, as shown in Figure 5. Such a classification system could be quantified further to create a “Building Rating Value” (or BRV) that could be used to define the effectiveness of air treatment in a retrofitted building. One such proposed method is the “Building Protection Factor” that is used to define the percentage of occupants protected from a biological agent release in a building (Kowalski, 2003).

Defining the air cleaning ability of a whole building, however, may be beyond the intended scope of this proposed standard. At the same time, the in-place testing of an air treatment system may be unavoidable. This aspect of the proposed standard can be revisited once the fundamental components are complete.

SAFETY AND HEALTH REQUIREMENTS

Exposure to UV radiation is hazardous to humans as well as other animals and plants. Guidelines have been established for occupational exposure by NIOSH. Also of concern is the production of potentially hazardous contaminants, such as ozone, for which exposure limits also have been set. Ozone levels are often quite low and can be measured, monitored, or controlled if necessary. Other chemical byproducts due to UV exposure of airborne microbes are possible but this area has not received much conclusive study. Under normal conditions, the quantities of air borne microbes have such a vanishingly small mass that their potential byproducts are unlikely to produce levels that approach a TLV or PEL. This is an area, however, that may require further research.

UV lamps that are breakable may not be suitable for every application (i.e., the food industry). UV lamps that contain mercury may require special handling and disposal. Most of these subjects are adequately addressed in other guidelines and standards and these can be referenced for further information or reiterated in the current proposed standard.

CONCLUSIONS

The development of an international standard for the performance and testing of UVGI systems is a daunting challenge that encompasses many fields and has such a broad scope that it will require the cooperation of many academic and industrial leaders in the UVGI industry, microbiology, and other relevant fields. Since the demand for air treatment systems has outstripped the available knowledge base, it is essential that such a standard be developed as quickly as is practical, especially in light of recently accelerated concerns about bioterrorism. The Ultraviolet Air Treatment Topical Group of the International Ultraviolet Association has brought together many of the major players in academia and industry, and we hope that this will lead to a significant change in the current philosophy of building science — the widespread adoption of air treatment in building design. The corresponding reduction in the transmission of indoor airborne diseases that would surely result would be a major first step towards the possible future eradication of the many respiratory diseases that currently threaten mankind around the globe.

Effectiveness of UVC Light to Mitigate Coronavirus (COVID‑19)

What are Coronaviruses?

Coronaviruses (CoV) are a family of enveloped viruses that were first discovered in the 1960s. Coronaviruses are most commonly found in animals, including camels and bats, and are not typically transmitted between animals and humans. However, six strains of coronavirus were previously known to be capable of transmission from animals to humans, the most well-known being SARSCoV (Severe Acute Respiratory Syndrome Coronavirus), responsible for a large outbreak in 2003, and MERS-CoV (Middle East Respiratory Syndrome Coronavirus), responsible for an outbreak in 2012. COVID-19 is caused by a coronavirus, which was initially named 2019-novel Coronavirus, or 2019-nCoV. On February 12, 2020, International Committee on Taxonomy of Viruses named the virus SARS-CoV-2, or Severe Acute Respiratory Syndrome Coronavirus-2. The Committee determined that this coronavirus was the same species as SARS-CoV, the virus that caused a global outbreak of a respiratory illness in 2003, but a different strain, hence the designation “2”.

Source: https://www.cdc.gov/coronavirus/2019-ncov/faq.html

Government / Industry Recommendations for Airborne Infection Control

CDC

Interim Infection Prevention and Control Recommendations for Patients with Confirmed Coronavirus Disease 2019 (COVID-19) or Persons Under Investigation for COVID-19 in Healthcare Settings.

https://www.cdc.gov/coronavirus/2019-ncov/infection-control/control-recommendations.html?CDC_AA_refVal=https%3A%2F%2Fwww.cdc.gov%2Fcoronavirus%2F2019-ncov%2Fhcp%2Finfection-control.html

CDC recommends the use of Ultraviolet Germicidal Irradiation (UVGI) as one of the effective technologies to minimize the spread of airborne microorganisms.

Implement Environmental Infection Control

Detailed information on environmental infection control in healthcare settings can be found in CDC’s Guidelines for Environmental Infection Control in Health-Care Facilities (https://www.cdc.gov/mmwr/preview/mmwrhtml/rr5210a1.htm) and Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Healthcare Settings [section IV.F. Care of the environment, https://www.cdc.gov/infectioncontrol/guidelines/isolation/index.html].
https://www.cdc.gov/infectioncontrol/pdf/guidelines/environmental-guidelines-P.pdf

ASHRAE Guidance

ASHRAE has developed proactive guidance ashrae.org/COVID19 to help address coronavirus concerns with respect to the operation and maintenance of HVAC systems. These include ASHRAE’s recently approved position document on airborne infectious diseases and links to the latest practical standards and guidelines.

ASHRAE recommends the following strategies of interest to address disease transmission: dilution ventilation, laminar and other in-room flow regimes, differential room pressurization, personalized ventilation, source capture ventilation, filtration (central or unitary), and UVGI (upper room, in-room, and in the airstream).

How Does UV Air Disinfection Help Combat Coronaviruses?

Coronavirus is highly susceptible to germicidal UV irradiation. The table below shows that the susceptibility of coronavirus to UV is greater than 3 times compared to the influenza (common cold) virus.

 

 

Delivering the Correct UV Dose for Coronavirus

The application challenge is to ensure the targeted organism is exposed to sufficient UV dose in the available space and time of UV exposure.

To ensure the proper dose is applied, our proprietary software is used to model the lamp quantity and system arrangement needed for the specific application. The output of this modeling produces a very detailed report showing intensity distribution and kill rates. Factors impacting dose include: spatial constraints, airflow volume, speed, temperature, and UV device geometry and intensity.

Third-Party Validation of UVC Effectiveness

UVDI has also conducted independent third party validation of UV efficacy against airborne bacteria and viruses, where MS2 macrophage was used as a surrogate for all viruses.

 

 

UVDI V-MAXTM Air Disinfection for HVAC Systems

 

 

In-Duct Air Disinfection System

  • Designed for duct-mounting parallel to the airstream providing optimum UV exposure
  • Fixtures can be mounted internally or externally on the duct
  • Configurable to meet airstream kill rates up to 99% – backed by computational models to ensure performance
  • Prewired lamp connection reduces installation time
  • Low power consumption with universal voltage input • Available in 21″, 33″, 48″ and 61″ lamp lengths

 

 

AHU Air Disinfection System

  • Easy to install in both existing and new equipment
  • Scalable design to fit any plenum size
  • Lamps can be easily mounted on vertical supports
  • Configurable to meet airstream kill rates up to 99% – backed by computational models to ensure performance
  • Minimal space required for installation
  • Negligible pressure drop
  • Low power consumption with universal voltage input
  • Available in 21″, 33″, 48″ and 61″ lamp lengths

Guidance for Building Operations During the COVID-19 Pandemic

The HVAC systems in most non-medical buildings play only a small role in infectious disease transmission, including COVID-19.1 Knowledge is emerging about COVID-19, the virus that causes it (SARS-CoV-2), and how the disease spreads. Reasonable, but not certain, inferences about spread can be drawn from the SARS outbreak in 2003 (a virus genetically similar to SARS-CoV-2) and, to a lesser extent, from transmission of other viruses. Preliminary research has been recently released, due to the urgent need for information, but it is likely to take years to reach scientific consensus.

Even in the face of incomplete knowledge, it is critically important for all of us, especially those of us in positions of authority and influence, to exercise our collective responsibility to communicate and reinforce how personal choices about social distancing and hygiene affect the spread of this disease and its impact not just on ourselves, but on our societal systems and economy. The consequences of overwhelming the capacity of our healthcare systems are enormous and potentially tragic. The sooner we “flatten the curve,”2 the sooner we can return to safer and normal economic and personal lives.

According to the WHO (World Health Organization), “The COVID-19 virus spreads primarily through droplets of saliva or discharge from the nose when an infected person coughs or sneezes….” Talking and breathing can also release droplets and particles.3 Droplets generally fall to the ground or other surfaces in about 1 m (3 ft), while particles (aka aerosols), behave more like a gas and can travel through the air for longer distances, where they can transmit to people and also settle on surfaces. The virus can be picked up by hands that touch contaminated surfaces (called fomite transmission) or be re-entrained into the air when disturbed on surfaces.

SARS infected people over long distances in 2003,4 SARS-CoV-2 has been detected as an aerosol in hospitals,5 and there is evidence that at least some strains of it remain suspended and infectious for 3 hours,6 suggesting the possibility of aerosol transmission. However, other mechanisms of virus dissemination are likely to be more significant, namely,

  • direct person to person contact
  • indirect contact through inanimate objects like doorknobs
  • through the hands to mucous membranes such as those in the nose, mouth and eyes
  • droplets and possibly particles spread between people in close proximity.

For this reason, basic principles of social distancing (1 to 2 m or 3 to 6.5 ft), surface cleaning and disinfection, handwashing and other strategies of good hygiene are far more important than anything related to the HVAC system.7 In the middle-Atlantic region of the United States where I work, malls, museums, theaters, gyms and other places where groups of people gather are closed and there are “stay at home”8 orders. This is a “game” of chance, and the fewer individuals who come in close contact with each other, the lower the probability for spread of the disease. Since symptoms do not become apparent for days or weeks, each of us must behave as though we are infected.

Other public buildings, considered essential to varying degrees, remain open. These include food, hardware and drug stores, and of course, hospital and health-care facilities (which are beyond the scope of this article). Anecdotally, some universities are allowing some or all faculty, staff and graduate students to conduct essential research and online classes. Banks and other service organizations are open to staff and are receiving customers by appointment only, and private and government workplaces are open with work at home for some or all encouraged or mandated.

For those buildings that remain open, in addition to the policies described above, non-HVAC actions include:

  • Increase disinfection of frequently touched surfaces.
  • Install more hand sanitation dispensers, assuming they can be procured.
  • Supervise or shut down food preparation and warming areas, including the office pantry and coffee station.
  • Close or post warning signs at water fountains in favor of bottle filling stations and sinks, or even better, encourage employees to bring their water from home. Once the basics above are covered, a few actions related to HVAC systems are suggested, in case some spread of the virus can be affected:
  • Increase outdoor air ventilation (use caution in highly polluted areas); with a lower population in the building, this increases the effective dilution ventilation per person.
  • Disable demand-controlled ventilation (DCV). • Further open minimum outdoor air dampers, as high as 100%, thus eliminating recirculation (in the mild weather season, this need not affect thermal comfort or humidity, but clearly becomes more difficult in extreme weather).
  • Improve central10 air filtration to the MERV-1311 or the highest compatible with the filter rack, and seal edges of the filter12 to limit bypass.
  • Keep systems running longer hours, if possible 24/7, to enhance the two actions above.
  • Consider portable room air cleaners with HEPA filters.
  • Consider UVGI (ultraviolet germicidal irradiation), protecting occupants from radiation,13 particularly in high-risk spaces such as waiting rooms, prisons and shelters.

Construction sites present unique challenges. Much, but not all, construction work has the recommended social distancing; much, but not all, is outdoors or in partially enclosed and therefore well-ventilated buildings; and many, but not all, workers already use personal protective equipment such as masks14 and gloves. Governments in some locations have mandated closure of construction sites, while in others work proceeds.15 Engineers who perform field observations, commissioning or special inspections must consider what work can be postponed, performed remotely, or conducted using photographic documentation, and what personal precautions to take when site visitation is unavoidable.

If you, the reader, are called upon to advise building operators, please use the above general guidance, and be sure to combine it with knowledge of the specific HVAC system type in a building and the purpose and use of the facility. Like all hazards, risk can be reduced but not eliminated, so be sure to communicate the limitations of the HVAC system and our current state of knowledge about the virus and its spread.

We all have a role to play to control the spread of this disease. HVAC is part of it and even more significant are social distancing, hygiene and the influence we can have on personal behavior

Thanks to William P. Bahnfleth, Ph.D., P.E., Presidential Member/Fellow ASHRAE, Lew Harriman, Fellow ASHRAE, Yuguo Li, Ph.D., Fellow ASHRAE, Andrew K. Persily, Ph.D., Fellow ASHRAE, and Pawel Wargocki, Ph.D., Member ASHRAE for their review of preliminary drafts of this article. Any errors that remain are the author’s alone.