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The procedure below should be followed whenever possible. The unit will still provide incrementally more air cleaning than having no air cleaner at all.

In a given room, the larger the CADR, the faster it will clean the room air. The label also shows the largest room size in square feet, ft 2 that the unit is appropriate for, assuming a standard ceiling height of up to 8 feet.

If the ceiling height is taller, multiply the room size ft 2 by the ratio of the actual ceiling height ft divided by 8. The CADR program is designed to rate the performance of smaller room air cleaners typical for use in homes and offices. For larger air cleaners, and for smaller air cleaners whose manufacturers choose not to participate in the AHAM CADR program, select a HEPA unit based on the suggested room size ft 2 or the reported air flow rate cfm provided by the manufacturer.

Consumers might take into consideration that these values often reflect ideal conditions which overestimate actual performance. For air cleaners that provide a suggested room size, the adjustment for rooms taller than 8 feet is the same as presented above.

If the ceiling height is taller, do the same calculation and then multiply the result by the ratio of the actual ceiling height ft divided by 8. Using ductwork and placing the HEPA system strategically in the space can help provide desired clean-to-less-clean airflow patterns where needed.

Example 2. Thus, the increased ACH and lower k value associated with the portable HEPA filtration unit reduced the wait time from the original 5 hours and 45 minutes to only 1 hour and 24 minutes, saving a total of 4 hours and 21 minutes before the room could be safely reoccupied. Adding the portable HEPA unit increased the effective ventilation rate and improved room air mixing. Ultraviolet germicidal irradiation UVGI , otherwise known as germicidal ultraviolet GUV , is a disinfection tool used in many different settings, such as residential, commercial, educational, and healthcare settings.

The technology uses ultraviolet UV energy to inactivate kill microorganisms, including viruses, when designed and installed correctly. However, UVGI can inactivate viruses in the air and on surfaces. These professionals can assist by doing necessary calculations, making fixture selections, properly installing the system, and testing for proper operation specific to the setting.

These fixtures disinfect air as it circulates from mechanical ventilation, ceiling fans, or natural air movement. The advantage of upper-room UVGI is that it disinfects the air closer to and above people who are in the room. For example, a rectangular-shaped waiting room with 10—30 occupants will require 2—3 upper-air UVGI fixtures. As part of system installation, care must be taken to control the amount of UV energy directed or reflected into the lower occupied space below levels recognized as safe.

Reputable UVGI manufacturers or experienced UVGI system designers will take the necessary measurements and make any required adjustments to prevent harmful UV exposures to people in the space. Potential Application: Can be used in any indoor environment; most useful in spaces highly occupied with people who are or may be sick. These systems are designed to serve one of two purposes:.

These devices produce relatively low levels of UV energy. This energy is continually delivered 24 hours a day, which is why they are effective. Coil treatment UVGI devices are not designed for disinfecting the air and should not be installed for the purpose of air disinfection. Air disinfection systems are often placed downstream of the HVAC coils. This location keeps the coil, drain pan, and wetted surfaces free of microbial growth and also disinfects the moving air.

Aside from the wavelength, a major difference between the two technologies is that standard UVGI systems are specifically designed to avoid exposing people to the UV energy, while many far-UV devices are marketed as safe for exposing people and their direct environment to UV energy. A review of peer-reviewed literature indicates that far-UV wavelengths can effectively inactivate microorganisms, including human coronaviruses, when appropriate UV doses are applied.

Questions remain about the mechanisms of killing microorganisms and overall safety. Far-UV might prove to be effective at disinfecting air and surfaces, without some of the safety precautions required for standard UVGI. Far-UV devices are best viewed as new and emerging technology. CDC does not provide recommendations for, or against, any manufacturer or product.

There are numerous technologies being heavily marketed to provide air cleaning during the ongoing COVID pandemic. Common among these are ionization, dry hydrogen peroxide, and chemical fogging disinfection. Some products on the market include combinations of these technologies. These products generate ions, reactive oxidative species ROS, which are marketed using many names , or chemicals into the air as part of the air cleaning process.

People in spaces treated by these products are also exposed to these ions, ROS, or chemicals. This does not necessarily imply the technologies do not work as advertised.

As with all emerging technologies, consumers are encouraged to exercise caution and to do their homework. Registration alone, with national or local authorities, does not always imply product efficacy or safety. Consumers should research the technology, attempting to match any specific claims against the intended use of the product. Consumers should request testing data that quantitively demonstrates a clear protective benefit and occupant safety under conditions consistent with the intended use.

When considering air cleaning technologies that potentially or intentionally expose building occupants, the safety data should be applicable to all occupants, including those with health conditions that could be aggravated by the air treatment.

In transient spaces, where average exposures to the public may be temporary, it is important to also consider occupational exposures for workers that must spend prolonged periods in the space.

Preferably, the documented performance data under as-used conditions should be available from multiple sources, some of which should be independent, third-party sources. Unsubstantiated claims of performance or limited case studies with only one device in one room and no reference controls should be questioned. At a minimum, when considering the acquisition and use of products with technology that may generate ozone, verify that the equipment meets UL standard certification Standard for Electrostatic Air Cleaners for production of acceptable levels of ozone, or preferably UL standard certification Environmental Claim Validation Procedure ECVP for Zero Ozone Emissions from Air Cleaners which is intended to validate that no ozone is produced.

Carbon dioxide CO 2 monitoring can provide information on ventilation in a given space, which can be used to enhance protection against COVID transmission. Strategies incorporating CO 2 monitors can range in cost and complexity. However, greater cost and complexity does not always mean greater protection.

Traditionally, CO 2 monitoring systems are expensive, require extensive knowledge to accurately install and set up, and require sophisticated control programs to effectively interact with the building heating, ventilation and air-conditioning HVAC systems in real time. They were not designed to protect building occupants from disease transmission.

As the current pandemic response has progressed, this technology has been marketed as a potential tool for providing an indication of building ventilation efficacy, leading to questions about whether monitoring indoor CO 2 concentrations can be used as a tool to help make ventilation decisions.

In some well-designed, well-characterized, well-maintained HVAC environments, the use of fixed CO 2 monitors can be informative. When used, these monitors are often incorporated into demand-controlled ventilation DCV systems that are designed with a primary intent of maximizing energy efficiency through reductions in outdoor air delivery.

However, guidance throughout the pandemic has been to exceed minimum ventilation whenever possible, in addition to masking, physical distancing, enhanced filtration, and other intervention-focused considerations. Fixed-position CO 2 monitors measure CO 2 concentration as an indicator of the number of people in the space.

The number of CO 2 sensors, the placement of those sensors, and their calibration and maintenance are collectively a large and complex issue that must not be overlooked. For example, the CO 2 concentration measured by a fixed, wall-mounted monitor may not always represent the actual concentrations in the occupied space. If air currents from the room HVAC, or even make-up air from windows, flows directly over this monitor location, the corresponding concentration measurements will be artificially low.

If the room has good air mixing, the measured concentration should approximate the true concentration, but rooms are rarely well mixed, particularly in older buildings with aging ventilation systems or none at all. Changes in CO 2 concentrations can indicate a change in room occupancy and be used to adjust the amount of outdoor air delivered.

However, CO 2 concentrations cannot predict who has SARS-CoV-2 infection and might be spreading the virus, the amount of airborne viral particles produced by infected people, or whether the HVAC system is effective at diluting and removing viral concentrations near their point of generation.

As a simple example, a small room with three occupants will have the same level of CO 2 and hence the same outdoor air ventilation rate controlled by the DCV system whether no one has SARS-CoV-2 infection or whether one or more people are infected with the virus. Ventilation based on CO 2 measurements cannot recognize the increased risk of transmission in the second scenario.

A more modest, cost-efficient, and accurate use of CO 2 monitoring is the use of portable instruments combined with HVAC systems that do not have modulating setpoints based on CO 2 concentrations.

This documentation will be the CO 2 concentration benchmarks for each room under the HVAC operating conditions and occupancy levels.

One potential target benchmark for good ventilation is CO 2 readings below parts per million ppm. If the benchmark readings are above this level, reevaluate the ability to increase outdoor air delivery. If unable to get below ppm, increased reliance on enhanced air filtration including portable HEPA air cleaners will be necessary. Once the benchmark concentrations are established, take periodic measurements and compare them to the benchmarks.

Under the pandemic response, a pragmatic application of portable CO 2 measurement tools is a cost-effective approach to monitoring building ventilation. For COVID, the first steps in reducing the indoor concentrations of the virus are wearing face masks , physical distancing , and reducing occupancy levels.

Improved ventilation is an additional prevention strategy. For ventilation systems, increasing outdoor air above the code minimum requirements, increasing total ventilation, and increasing filtration efficiencies are more effective at controlling infectious disease transmission than controlling indoor temperature and humidity. Both temperature and humidity can influence the transmission of infectious diseases, including COVID, but that influence has practical limitations. However, this temperature is far outside the limits of human comfort and could damage some building materials.

So, elevated temperatures offer the potential for decontamination of SARS-CoV-2 virus in the air or on surfaces, but the use of increased temperature solely for decontamination is not generally recommended and is not realistic for occupied spaces. Another important consideration is that when the temperature in a space is elevated, the corresponding relative humidity level decreases.

Current evidence is not persuasive that humidity significantly reduces transmission of SARS-CoV-2 beyond the level resulting from good ventilation and filtration. However, the reductions are modest and there are outliers to these findings. Some HVAC systems can actively control both temperature and humidity. However, the majority of HVAC systems do not have dedicated humidification capabilities.

Some dehumidification happens during warmer months as a byproduct of cooling humid warm air below its dew point and causing water to condense out of the air. Less common is the ability to limit low humidity by introducing water vapor into the dry supply air.

Most existing residential and commercial buildings located in cold climates are not constructed to resist the corrosion and excessive moisture accumulation that can result from long-term, whole-building humidification. If additional winter humidification is used to maintain comfort and prevent excessive dryness of nasal and ocular membranes, first analyze the building enclosure to verify that condensation and moisture accumulation will not become a problem.

For commercial buildings that are properly constructed to allow for long-term humidification, and which have humidification capabilities already installed, there is no reason not to humidify the air to comfortable levels during the winter months.

In residential settings, portable in-room humidifiers may be used for sensory comfort and to reduce excessively low relative humidity levels. Higher humidity levels are not necessarily better and may lead to localized mold growth, mildew, and other long-lasting indoor air quality issues. Maintenance and cleaning of portable humidification systems is very important.

Change the water in the humidifier daily and maintain and clean the humidifier in accordance with manufacturer recommendations. While fans alone cannot make up for a lack of outdoor air, fans can be used to increase the effectiveness of open windows, as described in the CDC list of ventilation improvement considerations.

Fans can also be used indoors to improve room air mixing. Improved room air mixing helps distribute supplied clean air and dilute viral particle concentrations throughout the room, which reduces the likelihood of stagnant air pockets where viral concentrations can accumulate. As with all fan use during the COVID pandemic, take care to minimize the potential to create air patterns that flow directly across one person onto another:.

Fans can also enable clean-to-less-clean directional airflow. Such applications should be evaluated closely to avoid unintended consequences and only adopted when supported by a safety risk assessment. Barriers can physically separate spaces that are next to each other.

When used for infection control, the barrier is intended to prevent someone on one side of the barrier from exposing a person on the other side of the barrier to infectious fluids, droplets, and particles. Whether a barrier interferes with improved ventilation depends on how it is installed. Protective barriers can sometimes help improve ventilation, but they can sometimes hinder ventilation too.

Sometimes they have no effect on ventilation. Protective barriers can assist with improved ventilation when used to facilitate directional airflows or desired pressure differentials between clean and less-clean spaces. The barrier can be aligned with the intended airflow to help direct it towards a desired location, such as an HVAC return air grille or a portable air cleaner inlet. Example scenarios for this type of barrier deployment include those where there is a known source of potentially infectious aerosols, such as a dental operatory or COVID testing station.

Alternatively, the barrier might be placed between two areas to better isolate one side of the barrier from the other. In this configuration, the barrier can also assist the HVAC design scheme in establishing a desired pressure differential between the adjacent spaces.

If necessary, small pass-through openings or a retractable panel incorporated into the barrier can allow transfer of physical objects from one side to the other. When not carefully installed, barriers can sometimes hinder good ventilation.

Barriers can unintentionally interrupt the airflow distribution within a space, thus allowing a concentration build-up of human-generated or other aerosols that may remain suspended in the air for minutes to hours. In this case, people could be exposed to higher concentrations of infectious aerosols than they would without the barriers in place.

The larger the barrier, the greater the likelihood that this may occur. This testing can assist in evaluating airflow distribution within the occupied spaces. If stagnant air pockets are seen to occur, barrier redesign or reorientation can help to minimize the occurrence. Airflow distribution modifications such as adjusting the positioning of supply air louvers or the discharge of portable air cleaners can also assist in eliminating the development of stagnant air pockets.

The Clean Air in Buildings Challenge helps building owners and operators improve indoor air quality and protect public health. Create your clean indoor air action plan today.

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