Professional Documents
Culture Documents
Project Proposal
Project Proposal
Project Proposal
COVID 19
Submitted By,
IAN GICHIMU GITHEKO
SUPERVISED BY:
JULY, 2023
DECLARATION
I declare that this project proposal is my own work and has never been presented in
part or wholly to any institution for the award of any academic qualification.
…....................................... .................................
INDEX NO: DMDE/6132/09/019
…....................................... .................................
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TABLE OF CONTENTS
DECLARATION …......................................................................................................................ii
ABSTRACTION ..........................................................................................................................vii
CHAPTER 1 …..............................................................................................................................1
1.0 Introduction /Background .......................................................................................1
Problem Statement ....................................................................................................................1
Justification ...............................................................................................................................2
Objectives ..................................................................................................................................2
1.1.1 Main objective ......................................................................................................2
1.1.2 Specific objectives …............................................................................................2
Block Diagram ...........................................................................................................................3
Components ...............................................................................................................................3
CHAPTER 2 ..................................................................................................................................4
2.0 Literature Review …................................................................................................................4
CHAPTER 3 …..............................................................................................................................5
3.0 METHODOLOY .....................................................................................................................5
3.0.1 Introduction ................................................................................................................5
3.0.2 Block Diagram (s) of the system …............................................................................5
WORK PLAN …............................................................................................................................6
PROPOSED BUDGET ..................................................................................................................7
REFERENCES ..............................................................................................................................8
APPENDICES…...........................................................................................................................9
iii
ACRONYMS AND ABBREVIATIONS OR SYMBOLS
LED: Light emitting Diode
LCD: Liquid crystal Display
I: Current
R: Resistor
V: Voltage
iv
LIST OF FIGURES
v
LIST OF TABLES
vi
ABSTRACT
UV light sterilization effectively inactivates microorganisms by damaging the DNA of cells.
DNA is responsible for cell replication, thus damaging the structure of DNA render cells unable
to and unable to spread disease or virus.
The report basically analyses the design and construction of a Uv light cash sterilizer. It will help
sterilize cash and prevent the spread of Covid 19
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CHAPTER 1
1.0 Introduction/Background
Demand for protective equipment continues to outstrip production as the number of infectious
diseases increases globally. For day-to-day sterilization purposes, a fast, efficient and reliable
disinfection process is necessary. The use of UV light as a disinfection technique dates to about
1900s. In current practices, UV light of the appropriate wavelength, which is usually 100nm to
400nm, is generated by electrical discharge through low-pressure mercury vapor, enclosed in a
glass tube that transmits UV light. The resulting germicidal lamp produces UV light with a
wavelength that ranges from 200nm to 280nm. This wavelength is within the short wave, or C
band of UV light. UV-C has been shown to deactivate viruses, mycoplasma, bacteria and fungi.
It takes only 2 minutes to kill viruses with a 15W UV-C lamp with the peak germicidal
efficiency being 254nm. While UV-C lighting is good for disinfection, it’s very harmful to
humans. It can damage the skin cells and eyes hence it’s important to build a solution that does
not allow the light to escape and break down your own DNA.
With the UV-C cash disinfection cabinet, we can easily irradiate cash in the cabinet. There are
four things to do while calculating UV-C dosage. That is; distance, UV-C tube power, duration
and shadowing. As per calculations, it takes 2 minutes to kill viruses with a 15W lamp but to be
on the safer side, items should be irradiated for 5 minutes for good measure.
1
1.2 Justification
UV disinfection cabinets are simple to use and ensure sterility. It is used to kill microorganisms
without the requirement of heat or chemicals. UV-light is non-toxic and environmentally
friendly. The use of UV germicidal irradiation in healthcare settings has been well documented
and is used for decontamination in many institutions and even in biological safety cabinets. UV-
C irradiation is used to inactivate viruses, bacteria and other microorganisms, rendering them
incapable of replication. The effectiveness of viral inactivation by UV-C depends on the
delivered UV-C dose, which is a function of exposure time and irradiance, as well as the UV-C
source wavelength, the ability of the microorganism to resist UV-C degradation, and the surface
structure of the object being decontaminated. Some major advantages of UV-C over other
disinfection methods include rapid throughput, ease of use, low electrical power requirements,
absence of toxic or dangerous chemicals and relatively simple overall device design and
construction. UV-C methods are considered a decontamination process and not a sterilizing
process.
1.3 Objectives
2
1.4 Components and materials
LCD Display
Buzzer
Lid Sensor
UVC Tubes
Buttons
Metal Mesh
LEDs
ICs
Resistors
Capacitors
Diodes
Transistors
Transformer
Base frame
Screws and bolts
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CHAPTER 2
2.0 LITERATURE REVIEW
Germicidal Ultraviolet (GUV, also known as UVGI) uses ultraviolet light in the UV-C
wavelength range (200 nm to 280 nm) to inactivate microorganisms. Most systems use low
pressure mercury lamps which produce a peak emission around 254 nm. The approach is well
decontamination, ventilation/cooling coil treatment and in-room air disinfection. UV-C for
surface and air decontamination has to consider health and safety issues. Human exposure to
UV-C can cause significant eye and skin damage and hence UV lamps must be located within
In real use UVc light from these devices rarely passes through single layers of glass and double-
glazed units will usually inhibit its transmission, so most of the exposure risk is likely to be
associated with exposure to the irradiation effects if present in the room when a unit is switched
water or on a surface, and environmental conditions such as temperature and humidity. The
majority of laboratory and control experimental studies focus on bacterial pathogens; however, a
number consider viruses. Under laboratory conditions GUV has been shown to be effective
against bacteriophages on surfaces (Tseng and Li, 2007) and in air against influenza (McDevitt
et al 2012), adenovirus serotype 2 and MHV coronavirus (Walker and Ko, 2007). Several studies
show that activation reduces with increased humidity for both bacterial (Ko et al 2000) and viral
aerosols (McDevitt et al 2012). Walker’s study calculated a UV susceptibility constant for MHV
coronavirus of 0.37 m2 /J, which places it as one of the easier microorganisms to inactivate.
Darnell et al. (2004) showed that SARS-CoV-1 could be inactivated by UV-C to enable safe
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working with virus containing materials. Bedell et al (2016) showed a UV-C decontamination
device was able to inactivate MERS-CoV and MHV coronavirus at 1.22m, with almost a 6-log
reduction for MERS-CoV in 5 minutes. There is no data yet for SARS-CoV-2, but the data for
other coronaviruses suggest it is highly likely that it is susceptible to UV-C. UV-C devices are
widely used for room surface decontamination in healthcare settings. Such devices usually
comprise multiple UV-C lamps located on a portable trolley, usually in a carousel formation to
offer 360o delivery - that can be wheeled into a room and operated remotely to prevent occupant
exposure. Several studies have evaluated these devices in hospital settings and shown they can
inactivate a range of bacterial pathogens (Mahida et al 2013), (Beal et al., 2016). Devices are
shown to be easy to use and can rapidly disinfect rooms. A standard UV-C device showed 3 to 4
log reductions on petri-dish samples ((Mahida et al 2013) while a pulsed UV device was
combined with cleaning of high touch sites to give an overall 90% reduction (Beal et al., 2016).
A study also showed that a UV-C device led to a 1.37 log reduction on textiles inoculated with
Enterococcus faecium in a ward setting (Smolle et al., 2018). Shadowing is however a concern
and a study of ambulance decontamination indicated that some surfaces could be disinfected in
seconds while others took over 15 hours as they didn’t receive enough irradiation (Lindsley et
al., 2018). Several studies are currently exploring the use of UV-C as a viable approach to PPE
advocated to both reduce contamination of cooling coils leading to energy efficiency benefits
and to control infection transmission in ventilation systems with recirculation. This approach
may have some benefit in commercial UK buildings; however, UK hospital ventilation systems
(with a small number of specific exceptions) are 100% fresh air and hence UV-C installation will
have no benefit. The majority of work on application of UV-C devices for airborne infection
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control focuses on upper-room GUV. These are shielded UV-C units that create a band of
ultraviolet light above the heads of occupants. Airflow patterns within the room carry pathogens
from the occupied zone though the upper-room UV zone providing ongoing disinfection while
the room is occupied. The approach cannot achieve 100% disinfection; instead, it acts in a
similar way to increased ventilation by reducing the concentration of pathogens within the room
A key advantage of this type of system, compared with mobile UVc carousels, is that the
treatment is designed so that the room can remain occupied. There is good evidence from studies
(2009) repeated classic experiments conducted by Wells and Riley in the 1950’s and showed
77% reduction in human to guinea pig transmission. Chamber based studies show the
al 2000, Kanaan et al., 2015, Yang et al. (2012). There are several studies that have modeled
upper-room GUV (Noakes et al 2004, Sung and Kato 2010, Gilkeson and Noakes 2013, Kanaan
et al., 2015, Yang et al. 2012)) and shown that the effectiveness depends on the placement of the
lamps relative to the ventilation flow, and that the two need to be considered together when
designing a system. Zhu et al. (2014) modeled the application of an upper-room GUV system
combined with a ceiling fan to show that increased mixing in the room enhances the
effectiveness of the GUV. Noakes, Khan and Gilkeson (2015) developed a zonal model coupled
with the Wells-Riley infection model to show the potential impact of upper-room GUV on
infection risk could be comparable to doubling the ventilation rate. Modeling studies also show
that upper room GUV is unlikely to significantly impact the close-range transmission risk within
1-2m of the infected source. GUV can also be applied through enclosed systems located within a
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room. Larger systems are similar to a wall or ceiling mounted air conditioning unit, while
There are several such devices on the market and all show good single pass efficiency, however
their effectiveness in a room is dependent on their flow rate relative to the room size; many
devices have an insufficient air flow rate to be as effective in practice as claimed. There is recent
evidence to show that far-UV in the 200-222 nm wavelength range may be effective at
inactivating microorganisms without the risks to human health of conventional 254nm systems.
Several papers show the effectiveness and lack of skin damage in laboratory studies (Buonanno
et al., 2017, Narita et al., 2018, Welch et al., 2018), however there is not yet any evidence of
microbial inactivation from aerosol studies, chamber studies or real-world settings or any
evidence for safety in real-world settings. This is a promising technology that could enable more
effective disinfection than conventional UV-C, but needs substantially more research to prove it
is effective in a real-world setting. Guidelines on GUV systems are given by ASHRAE with
some information provided in CIBSE Guide A. CIE (2020) have also produced a position
statement on GUV which indicates that UV-C has significant potential but can be hazardous and
therefore must be installed with care. They recommend only using properly constructed products
which meet safety regulations and indicate that UV measurements to ensure human exposure
limits are not exceeded are important for any systems that are not fully enclosed. It should also
be noted that the effectiveness of GUV systems depends on the state of the lamps. The output of
UV-C lamps degrades with time and is also affected by dirt on lamp surfaces. Good maintenance
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CHAPTER 3
3.0 METHODOLOGY
3.0.1 Introduction
With the UV-C disinfection cabinet, we can easily irradiate cash inside the cabinet. According to
research there are four things to consider while calculating UV-C dosage. That is; distance, UV-
C tube power, duration and shadowing. As per calculations it takes 2 minutes to kill viruses with
a 15W lamp.
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3.3.1 TRANSFORMER
The aim of the transformer in this project is to step down voltage from 240 volts ac to 12 volts
ac. Therefore, step down laminated core transformer is the one used because it is designed to
work at a low frequency. The laminated core transformer is the one used here. This is because of
3.3.2 RECTIFICATION
The choice of the diode depends on the intended application. In our case, the diodes are required
to convert ac to dc. Therefore, rectifier diodes are the ones ideal for this work. Each of the four
diodes is required to carry the required current of 300mA and withstand a voltage of at least 12
volts. Therefore, the best diode for this is the one rated just above 300mA and above 12 volts.
Therefore, the ideal diode for this is IN4007. It has a current capacity of 1 ampere and peak
inverse voltage capacity of 1000 volts. Four of them will be used to form a four-diode bridge
rectifier.
Since our required output is 5 volts to power the microcontroller and 12 volts to power solenoid,
The operation of the reed switch is based upon the principle of magnetic induction. When a
magnet, whether permanent or electromagnetic, is in close proximity to a soft iron material the
soft iron magnetizes. Once magnetized there is nothing to distinguish a permanent magnet from
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an induced magnet. Hence, any other soft iron material in close proximity will also be turned into
WORK PLAN
PROPOSAL WRITING
AND SUBMISSION
COLLECTION OF
MATERIALS
DESIGN OF
DATA COLLECTION
AND ANALYSIS
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PROJECT REPORT
1. Transformer 1 700
2. 1N4007 diode 4 120
3. Switch on/off 1 80
4. Capacitor 4 240
5. 7805 IC 1 85
6. Resistors 10 300
7. LEDs 2 100
8. Reed sensor 1 300
9. 555 timers 1 200
10. UV bulbs 1 3500
11. Photo diode 1 200
12. LM 324 IC 1 300
13. Transistor 1 30
14. Strip board 1 100
15. Solder wire 6 meters 240
16. Connector wires 4 meters 140
17. Casing 1 750
18. PIC16F73 1 1600
19. Crystal 1 150
20. Typing and binding 1100
TOTAL 10085
Table 2: Proposed budget
Source of funding; myself
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REFERENCES
1. Haque, M.; Sartell, M.; McKimm, J.; Bakar, M.A. Health care-associated infections—An
Infection Worldwide;
3. FitzGerald, G.; Moore, G.; Wilson, A.P. Hand hygiene after touching a patient’s surroundings:
The opportunities most commonly missed. J. Hosp. Infect. 2013, 84, 27–31. [CrossRef]
4. Weber, D.J.; Rutala, W.A. Self-disinfecting surfaces: Review of current methodologies and
future prospects.
5. Saka, K.H.; Akanbi, A.A.; Obasa, T.O.; Raheem, R.A.; Oshodi, A.J.; Kalgo, Z.M. Pathogenic
aerobic bacterial
Med. Microb.
12
6. Russotto, V.; Cortegiani, A.; Raineri, S.M.; Giarratano, A. Bacterial contamination of
equipment in the intensive care unit. J. Intensive Care 2015, 3, 54. [CrossRef]
7. Brady, R.R.; Hunt, A.C.; Visvanathan, A.; Rodrigues, M.A.; Graham, C.; Rae, C.; Gibb, A.P.
Mobile
colonization,
and patient opinions and behaviours. Clin. Microbiol. Infect. 2011, 17, 830–835. [CrossRef]
8. Tagoe, D.N.A.; Baidoo, S.E.; Dadzie, I.; Tengey, D.; Agede, C. Potential sources of
transmission of hospital
acquired infections in the volta regional hospital in Ghana. Ghana Med. J. 2011, 45. [CrossRef]
9. Ustun, C.; Cihangiroglu, M. Health care workers mobile phones: A potential cause of
microbial
cross-contamination between hospitals and community. J. Occup. Environ. Hyg. 2012, 9, 538–
542. [CrossRef]
10. Adlhart, C.; Verran, J.; Azevedo, N.F.; Olmez, H.; Keinänen-Toivola, M.M.; Gouveia, I.;
Surface modifications for antimicrobial effects in the healthcare setting: A critical overview. J.
Hosp. Infect.
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11. Rutala, W.A.; Weber, D.J.; Healthcare Infection Control Practices Advisory Committee.
Guideline for
https://www.cdc.gov/
12. Musuuza, J.S.; Guru, P.K.; O’Horo, J.C.; Bongiorno, C.M.; Korobkin, M.A.; Gangnon, R.E.;
Safdar, N.
review and
13. McDonnell, G.; Russell, A.D. Antiseptics and disinfectants: Activity, action, and resistance.
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