ACT CleanCoat™ is based on a disruptive technology that is specifically engineered to fight harmful microbes. When ACT CleanCoat™ is applied to surfaces they become self-disinfecting and decompose microbes like bacteria, viruses, airborne mold spores, and chemical compounds like VOCs.
The coating is transparent and odorless and can be applied to all surfaces. Once exposed to light, it starts a photocatalytic reaction that decomposes microbes and purifies the air.
ACT CleanCoat™ is approved for use on all surfaces, including surfaces with direct food contact and has a non-rinse claim.
EVALUATED Effective Against Coronaviridae
Conclusion by Dr. Brill & Partner, GmBH
Therefore, after successful experiments with three non-enveloped viruses ACT CleanCoat™ is also effective against the so-called blood-borne viruses including HBV, HCV and HIV as well as against members of other virus families such as orthomyxoviridae (incl. all human and animal influenza viruses like H5N1 and H1N1), coronaviridae (MERS-CoV) and filoviridae including Ebola virus
In the presence of indoor or outdoor light, ACT CleanCoat™ uses Titanium dioxide (TiO₂) to turn natural humidity and oxygen into free radicals in a natural process called photocatalysis.
When TiO₂ is exposed to light, it generates electron-hole pairs that transform the humidity in the air into free radicals. Free radicals continuously decompose bacteria, viruses, and the volatile organic compounds that they come into contact with.
Titanium dioxide (TiO₂) is a naturally occurring oxide and is the key ingredient in ACT CleanCoat™. It has a wide range of applications, including as a paint pigment, sunscreen ingredient, and food additive. TiO₂ is a naturally occurring oxide.
Tested and approved
ACT CleanCoat™ has passed several European norm tests. The efficiency of ACT CleanCoat™ has also been reviewed and recognized by laboratories and agencies such as:
• European Chemical Agency, EU agency
• Danish Technical Institute, Denmark
• Dr Brill and Partner, GmbH, Germany
• ISI Food Protection, Denmark
• Danish Technical University, Environmental Engineering, Denmark
• Ministry of Environment and Food of Denmark, Denmark
• Chech Technical University, Czech Republic
• North Carolina State University, United States
• Mahidol University, Thailand
• Guangdong Institute of Microbiology, China
Summary of submitted test results
The product’s method of action is innovative when compared to how a standard surface disinfection product reduces microorganisms. Once applied to a surface and dried, the product produces a long-lasting anti-microbial effect.
Titanium dioxide surface treatment is a new and innovative product for disinfection. The preliminary laboratory results, as well as some clinical studies, show the product has a reducing effect on the number of microorganisms when applied on surfaces.
THE EFFECTS of ACT CleanCoat™
To be recognized as a biocide within the European Union, a product has to pass a biocidal EN-test and be registered with the European Chemical Agency.
Europäischen Normen (EN) are technical standards drafted and maintained by the European Committee for Standardization, the European Committee for Electrotechnical Standardization, and the European Telecommunications Standards Institute.
ACT CleanCoat™ has passed 10 EN-tests conducted on organisms, such as:
Mold and yeast
Learn moreSee Less
TiO2 is the most studied semiconductor photocatalyst, finding applications in various industrial and environmental applications, such as the removal of contaminants from both water and air or in sunscreens and coatings.
TiO2 is a well-known photocatalytic antimicrobial agent, in both its bulk (coating, micropowder), and nanometric form. The antimicrobial efficacy of TiO2 formulations depends on several parameters that include: concentration, contact time, intensity and wavelength of light, pH, temperature, availability of oxygen and target microorganism.
TiO2 nanoparticles were reported effective towards a large variety of microorganisms, including viruses, bacteria and fungi, with an efficiency influenced by the thickness of the microorganism’s surface structure, in the order of virus>bacterial wall>bacterial spore.
Within bacteria, the efficiency of nano-TiO2 was found to be in the order of Escherichia coli > Pseudomonas aeruginosa > Staphylococcus aureus > Enterococcus faecium > Candida albicans, reflecting again the dependence of the antimicrobial action to the complexity and density of the cell membrane.
Cleaning the air
Reduces air pollutants including volatile organic compounds (VOCs) such as formaldehyde, benzene, and acetone, as well as NOx. VOCs cause that typical drowsiness experience in a room with poor ventilation, new furniture, new carpets, or certain electronics.
ACT CleanCoat™ reduces the number of VOCs and odors (which are also carbon-based molecules) in the air, providing our clients with better indoor air quality.
Learn moreSee Less
Volatile organic compounds in 25 L Tedlar® bag* concentration (μg/m³) over time (minutes)
Black line: without ACT CleanCoat™ | Blue line: with ACT CleanCoat™
Test performed by the National Research Centre for the Working Environment, Hans Christian Budtz
* Tedlar® gas sampling bag
Field data, level of formaldehyde, during office hours.
Minimum 0 ppm, average 0.055 ppm.
08.00-22.00, office hours with light turned on
ACT CleanCoat™ used for air purification, Lars Schmidt Hansen, M.Sc., January 2019
In nature, mold is necessary to help dead organic material decompose. However, mold poses a significant challenge in buildings. Besides the unpleasant odor and possibly costly renovation of the building, there are serious health risks involved in living and working in a mold-infested environment.
Mold spores are basically everywhere, but with ACT CleanCoat™ they are decomposed before they even settle on a coated surface, inhibiting spore germination, or mycelium growth.
ACT CleanCoat™ has passed several European norm tests for mold and yeasts.
• EN 13624, Aspergillus brasiliensis
• EN 14562, Aspergillus brasiliensis
• EN 13624, Candida albicans (candida yeast)
• EN 14562, Candida albicans (candida yeast)
Learn moreSee Less
Extract from the report: Test of ACT CleanCoat™ by the quantitative suspension test for fungicidal activity according to EN 13624
Results by membrane filtration procedure
For each of the tested strains, the test dates and colony counts of the test suspension and the validation suspension are shown in Table 1, and the colony counts on the filters are shown in Table 2.After 60 min. exposure time, there were too many survivors of both test strains to allow a precise count; however, an estimate of the number of colonies was made in order to calculate an approximate reduction level. After 24 h exposure, there were no survivors of either strain.
Table 1. The colony count results of the test suspension and validation suspension for Aspergillus brasiliensis and Candida albicans.
|Strain||Date||Test susp. cfu/ml||Val. susp. cfu/ml|
Table 2. Colony counts of Aspergillus brasiliensis and Candida albicans after treatment with ACT CleanCoat™ from the test and control (A, B, C) filters for each strain.
C. albicans00ca. 500ca. 500169176198178144163
|Strain||Test (24 h)||Test (60 min.)||A||B||C|
|A. brasiliensis||0||0||ca. 300||ca. 300||91||96||100||104||109||94|
The log10 reduction is calculated as follows:
- Log10 reduction = log10 (initial cfu/ml in test mixture) – log10 (final cfu/ml after exposure)
The initial cfu/ml in the test mixture is 1/10 of the test suspension density (Table 2), since1 ml test suspension is used forpreparing10 ml test mixture.
For the membrane filtration analyses, 0.1 ml of the test mixture is taken out and filtered. No recovery of colonies in 0.1 ml gives a result of < 1 cfu/0.1 ml, corresponding to a final density after exposure of < 10 cfu/ml. Using the approximate counts after 60 min. exposure and10 cfu/ml after 24 h exposure for the calculations gives the following log10 reductions:
- Aspergillus brasiliensis: approx. 2.8 log10 reduction after 60 min, and min. 5.3 log10 reduction after 24 h
- Candida albicans: approx. 2.7log10 reduction after 60 min, and min. 5.4 log10 reduction after 24 h
THE CHEMISTRY behind ACT CleanCoat™
The natural decomposition of organic matter can be accelerated by the use of a photocatalyst, such as titanium dioxide (TiO₂).
Energy-rich electron-hole pairs are produced upon exposure to light (with energy above the TiO₂ band gap). When applied to any material these charge carriers interact with ambient oxygen and water, generating highly reactive hydroxyl radicals and superoxide.
These radicals can either directly attack the surrounding microbial matter or recombine via different pathways, forming hydrogen peroxide.
Hydroxyl radicals, superoxide radicals and hydrogen peroxide are the reactive oxygen species (ROS) ultimately responsible for the biocidal activity of ACT CleanCoat™ through non-selective oxidation of organic material.
The catalyst is never consumed during the reaction, ensuring a continuous process during the service life of the coating. The TiO₂ particles in ACT CleanCoat™ are specifically engineered to work in all environments.
Free radicals induce oxidative stress, and they attack all major classes of biomolecules, mainly polyunsaturated fatty acids, also known as lipids, of the cell membranes.
The free radicals in ACT CleanCoat™ work by oxidizing and attacking the cell membrane of microbes – in other words, the microbes decompose.
The oxidative degradation of lipids (known as lipid peroxidation) is very destructive, as it proceeds as a self-perpetuating chain reaction. After the destruction of the cell wall, the free radicals proceed to oxidize the cell core.
Due to the constant high oxidative rate of free radicals, the oxidation of the cells creates water, carbon dioxide, and minerals. Both the water and carbon dioxide will evaporate, leaving only the cells’ minerals on the surface.
PASSED European Norm Tests
|EN 13704||Bacillus subtilis|
|EN 13624||Aspergillus brasiliensis, Candida albicans|
|EN 13697||Aspergillus brasiliensis, Candida albicans, Pseudomonas aeruginosa, Staphylococcus aureus, Enterococcus hirae, Escherichia coli|
|EN 14562||Aspergillus brasiliensis, Candida albicans|
|EN 14348||Mycobacterium avium, M. terrae|
|EN 14563||Mycobacterium avium, M. terrae|
|prEN 16777||Adenovirus, Murine norovirus|
|EN 14476||Poliovirus, Adenovirus, Murine norovirus, EV-71, Influenza A, Influenza B|
|EN 13727||Pseudomonas aeruginosa, Staphylococcus aureus, E. hirae, Salmonella, MRSA|
|EN 14561||Pseudomonas aeruginosa, Staphylococcus aureus, Enterococcus hirae|