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UV-C light for Processing of Products
and Surfaces
Danny Bayliss, PhD
+44 (0) 1386 842130
linkedin.com/in/danny-bayliss-4a50b950
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Contents
• Introduction to UV-C light
• Applications of the technology
for surface inactivation
• Factors to consider when
specifying and validating a UV-C
system
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Principals and mechanisms
• Technology uses light to prevent microorganisms from growing
• Light is in the Band C part of the ultraviolet light spectrum (200-280 nm)
• Bacteria need direct exposure to the 254 nm light for inactivation
• UV-C light modifies microorganism DNA and prevents it from growing
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Microbial Susceptibility
• Level of susceptibility:
Bacteria and yeast> virus and bacterial spores >moulds
• Aspergillius brasiliensis (niger) being the most resistant
• Food products have complex matrix and surface topography that
influence inactivation and you are typically likely to get 1-2 log
reductions
• Smoother surfaces 3- 5 logs possible
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UV-C tunnel
• System consist 16 x 95 watt ‘high output’ UV-C
emitters
• Lamps top and bottom of a wire mesh belt
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UV-C transfer
systems
Images courtesy of Steve
O’Brien UV technology
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Images courtesy of Steve O’Brien UV technology
UV-C transfer systems
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Conveyor transfer system
Images courtesy of Richard
Little Jenton Group
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Images courtesy of Steve O’Brien UV technology
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UV-C transmission
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Validation considerations
• Things to consider when specifying a UV-C system and then
validating the system.
1. How many different products will be treated and their differences
2. Shadowing and shielding management with the system
3. Where is the dark (low dose) region in the tunnel or chamber.
4. Monitoring the dose
5. Target organisms and log reductions
6. Throughput and floor space
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Multiple products
• Furthest from the lamps needs to be validated as it will receive the lowest
intensity of light (mW/cm2)
• Items closer to the lamps will be overdosed so need to consider quality
impacts
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Shadowing and shielding
• Belt and its support structures
will impact the dose delivered
to the underside of the product
• Systems can index products to
move it on the belt to expose
shielded areas
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Dose monitoring
• Systems can vary so
be aware!
• Different spectral
ranges
• Use vs how it was
calibrated
• Alternative quick checks
Image provided by Claes Lindahl at Intellego Technologies
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Virus surrogate inactivation
• MS2
bacteriophage
(RNA virus)
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Virus surrogate inactivation
• Murine
Norovirus
(RNA virus)
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Advantages Limitations
Broad antimicrobial activity Low penetration
No residues after decomposition Shadowing issue
Non-thermal, dry decontamination
method
Only surface decontamination
Do not store hazardous materials Can cause some oxidation and
damage the product at high dosages
Relatively low running costs/lack of
extensive safety equipment
Technical advantages/limitations
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Summary
• Technology has a wide range of possible application for surface microbial
reductions
• Validation of all the parameters that can impact on the efficacy of the
process need to be considered so suitable worst case conditions can be
tested.
• Suitability of the product needs to be determined on a case by case basis
• Important to consider the organisms targeted and the dosages required and
the impacts on key nutrient components
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Thanks you for listening!!!
• Any questions or comments please get in touch
Danny Bayliss, PhD
New Technology Research Lead
44 (0) 1386 84 2130
linkedin.com/in/danny-bayliss-4a50b950