Nikhil Pal Project Mba1
Nikhil Pal Project Mba1
Father’s name-
RAM PRAKASH
BATCH 2023-2024
ACKNOLEDGEMENT
INDEX
SR.NO.
CONCEPT PAGE
1. Introduction 4
2. Scope of innovation 5
3.
Feasibility
1.Financial 6 to 8
2.operational
9to26
3.Bricks manufacturing process
6.Implementation guide
5. Implementation Guide 27
6. Conclusion 28to29
7. proposal 30
8. Abbreviation 31
9. Refrences 32to38
4 of 38
Introduction
Cigarette butts (CBs) are the most common type of waste material discarded in the world. In 2016, an
estimated 5.7 trillion cigarettes were consumed around the globe . While, in Australia, 24 billion
cigarettes were consumed, of which seven-billion were disposed of incorrectly . That is, up to two-thirds
of every smoked cigarette is littered to the environment . Numerous countries have implemented strong
tobacco control regulations, and a significant decline in cigarette consumption has been observed .
Despite this, it is estimated that the number of tobacco smokers is set to increase by seven- and 24-
million in Nigeria and Indonesia, during the period 2015 and 2025 . This is due to further growth in the
market and population growth .There are over 4000 chemicals present in a cigarette, seventy-two of
which are known to be cancer-causing carcinogens . The main toxic agents include carbon monoxide,
argon, aromatic hydrocarbons, hydrogen cyanide, phenol, nitrogen oxides, formaldehyde, acetaldehyde,
acetone, benzene, ammonia, and pyridines . The filter of a cigarette is made of cellulose acetate fibers,
whereby the filter modifies the particulate smoke components through particle retention . However,
cellulose acetate filters have poor biodegradability and they can take up to 10 years to decompose under
normal environmental conditions . Therefore, when CBs are freely dispersed in the environment, they
pose a critical problem in terms of toxic waste for the urban and aquatic life . Aquatic animals regularly
consume CBs mistaking it for food and they have been found in the stomachs of fish, birds, sea turtles,
and other creatures, leading to serious digestive issues .
As the world’s population increases, the number of CBs being littered is likely to rise
drastically. In Australia, CBs were reported as the most common source of rubbish collected,
representing 91.5% under the miscellaneous category . As a result, it is becoming more imperative
that an effective solution for this environmental problem be found and implemented.
Torkashvand and Farzadkia (2019) focused on developing control models for CB littering, while
Marinello et al. (2019) analysed possible recycling techniques for CBs and evaluated the disadvantages
and advantages of those methods studied . In contrast, Kurmus and Mohajerani (2020) reviewed key
research studies on the recycling of CBs and investigated their toxicological properties . The paper
explored the effectiveness, sustainability, and efficiency of those recycling methods. A major recycling
method reviewed involved the development and the use of encapsulated CBs in asphalt concrete with
acceptable physical and mechanical properties . Furthermore, CBs have been used in several
applications in small scales in order to produce items, such as pillows, plastic furniture, and shipping
pallets. However, the credibility and sustainability of any method and product for recycling CBs must
be investigated in terms of toxicity, leachability, and life cycle analysis.
Previous studies conducted by Mohajerani et al. (2016) tested the physical and mechanical
properties, emissions, and energy savings of fired clay bricks incorporated with CB content,
and presented promising results. The proposal was to incorporate 1% CB content by weight in 2.5% of
the world brick production to solve a global waste catastrophe
However, further testing and analysis are required for the brick manufacturing industry and
government organizations to confirm that recycling CBs in fired clay bricks is a feasible and beneficial
proposal. The objective of this study is to present and discuss some of the results of an ongoing
research on recycling CBs in fired-clay bricks. It includes the calorific value of CBs and energy savings,
laboratory study on the manufacturing and properties of bricks containing CBs, CB incorporation
in the brick manufacturing process on an industrial scale, pilot bacteriological investigations of
CBs, and possible CB odour reduction and sterilisation methods.
5 of 38
Scope of innovation
5. *Public Awareness:* The adoption of such bricks could raise awareness about
the environmental impact of cigarette butt disposal, encouraging responsible
habits.
Feasibility
1.financial feasibility
1. *Environmental Impact:* Recycling cigarette butts into bricks can contribute to waste
reduction and environmental sustainability, addressing the issue of cigarette litter.
2. *Resource Efficiency:* Utilizing a waste product for construction material may reduce
the need for traditional raw materials, potentially lowering production costs.
*Challenges:*
1. *Processing Costs:* The process of collecting, cleaning, and processing cigarette butts
can incur expenses, affecting the overall production cost.
3. *Perception and Acceptance:* The construction industry may need time to adopt and
trust this unconventional material, impacting market acceptance and demand.
Estimated cost.
7 of 38
2.oper
ational feasibility
. *Collection and Sorting:* Establishing a systematic and efficient system for
collecting and sorting cigarette butts is crucial. This involves setting up
collection points and ensuring a steady supply of raw materials.
Q1 = q × m1 (1)
Q2 = q × m2 − CV × m3 (2)
It is estimated that, if 2.5% of all the bricks produced annually around the world include 1% CB
content, the energy consumption of the process can be reduced by approximately 20 billion MJ (from
the calorific value of 1% CBs with 9.3% energy saving) . This approximately equates to the power used
by one million homes every year in the State of Victoria, Australia. Therefore adding 1% CBs (about 20
kg/m3) to the brick clay results in significant energy savings, solves the CB pollution globally, and
tangibly reduces the environmental impact of the brick manufacturing industry whilst providing
financial savings to manufacturers through the reduction of energy for firing bricks.
The manufacturing process of the bricks first involved drying the soil and CBs (if any) in an oven
for 24 h at 105 ◦C. The soil was taken out of the oven and crushed into finer particles to pass
through a sieve size of 2.38 mm. The soil and oven dried CBs were then placed inside a 20L
capacity Hobart mechanical mixer and mixed for a total of 25 min. The calculated water content of
15.5% was gradually added during the mixing process. After the mixing was complete, the mixtures
were sealed in airtight plastic bags and then left to settle for a period of 48 h to uniformly distribute
moisture throughout the mix.
The next step was to compact the mixes while using a Servopac Gyratory compactor with
a pressure of 240 kPa. A cylindrical mould was used during the compaction process. The moulds were
100 mm in diameter, in which a predetermined mass of soil was placed inside the mould in order
to yield bricks with heights of approximately 50 mm.
After compaction, the samples were air dried for 24 h before being placed in an oven for 24 h
at 105 ◦C. After being removed from the oven, the samples were fired in an electric furnace at 1020
◦
C for 3 h. The height, diameter, and weight of the bricks were measured while using a digital
caliper and electronic scale at each stage of the manufacturing process to compute the diametric
and height shrinkage of the bricks.
The bricks were tested according to AS/NZS 4456.1:2008 after they were removed from the
furnace and allowed to cool to room temperature . The compressive strength, initial rate of absorption
(IRA), cold water absorption, shrinkage, and density were computed. Compressive strength tests were
conducted on three samples from each mix using a Material Testing Machine (MTS), while the cold-
water absorption and IRA testing were completed using a water bath.
TC = 0.0558e0.0014Dd (5)
Where,
These results confirm the findings in Mohajerani et al. (2016) . Investigations into the
leachates from manufactured CB bricks have already been conducted . The Australian Bottle
Leaching Procedure (ABLP) and the Toxicity Characteristics Leaching Procedure (TCLP) were both
used on crushed bricks and solid bricks . The testing was conducted on bricks containing 2.5, 5.0, 7.5,
and 10.0% CB content. It was found that heavy metal concentrations were well below the levels
stipulated by the USEPA and the Environmental Protection Agency of Victoria for concentrations of
10% and lower CB content . Additionally, a comprehensive leachate study on leachate analysis of
heavy metals in cigarette butts and bricks incorporated with cigarette butts has been carried out
based on ABLP (2019) and USEP (2013) .
Figure 2. Method 1—The addition of whole cigarette butts (CBs) into the Automatic Manufacturing Process.
CBs are directly incorporated in stage 3. Water is added throughout the blending stage, as
moisture within the mixture entraps chemicals and mitigates potential airborne particles.
Figure 3. Method 2—Addition of pre-shredded CBs into the Automatic Manufacturing Process.
It is important to understand that the actual shredding of the CBs must be performed in a fully
enclosed environment, such as an enclosed industrial shredder. This is necessary, as it keeps the dust
and chemicals from spilling out into the environment. Enclosed shredding minimises
environmental pollution and the exposure of personnel that could occur when compared to
shredding in an open air environment. When compared to method 1, as the CBs are already pre-
shredded, it is expected that there will be improved uniformity in particle size and distribution within
the mix, leading to clay bricks with more uniform properties.
Figure 4. Method 3—Addition of a concentrated CB pre-mix into the Automatic Manufacturing Process.
4.1.4. Appropriate Personal Protective Equipment for the Automatic Manufacturing Process
There is a possibility when dealing with CBs that the chemicals that are present in CBs may be
distributed into the air with other dust particles. Therefore, it is essential that all workers exposed to
excessive dust particles be equipped with dust masks. If moisture is added to the mixture at the same
time as the introduction of CBs, then the risk of inhalation of airborne particles is drastically reduced,
or possibly mitigated, as mentioned in the above methods. However, there is the potential for leachates
contaminating surfaces, such as conveyor belts, and mills, etc., due to the potential for the moisture to
introduce metals to the environment . As a result, workers encountering this mixture or associated
surfaces should also wear protective gloves and long-sleeve clothing.
4.1.5. Odour Issues and Reduction Methods for the Automatic Manufacturing Process
Odour can be a significant issue that is introduced through the incorporation of CBs into
the automatic brick making process. Odour is caused by the diffusion of chemicals that are entrapped
within CBs being released, such as volatile organic compounds (VOCs) . Odour can be displaced by air
current or diffusion, both of which rely upon the environmental conditions and time. The smell is a
biochemical reaction, where VOCs attach themselves to the olfactory receptors that are located in the
nose. These receptors then send an electrical signal to the brain that is perceived as odour . Not all
VOCs have an odour associated with it, for example, methane, which is an odourless chemical . Due to
smell being the human perception of the physical world, it is hard to physically or chemically measure
and quantify smell, as even the smallest amount of VOC can produce an odour. This is a problem,
because CBs are introduced in the blending stage, but the odour can persist until firing of the CB
bricks occurs (stages 3–7).
Odours themselves contain four attributes that humans can detect and describe. These attributes
include the detection threshold, intensity, character, and hedonic tone. The detection threshold is
the minimum amount of chemicals needed to detect odour; intensity is how strong the odour is
upon and after detection; character is defined as what the odour smells like; and, hedonic tone is how
pleasant the odour is to smell . Out of the four attributes, only two of them are quantifiable—
detection threshold and intensity. The detection threshold is defined as the point at which 50% of the
population (normally a panel of six people) can detect an odour and is recorded numerically as one
odour unit per metre cube 1 o.u./m3 . The intensity of an odour can be quantified using the Weber–
Fechner law, in which an increase in concentration is perceived as a large increase in intensity when the
concentration value is small. The equation intensity versus concentration is a logarithmic relation
(Equation (6)), which means that, for CBs in the brick manufacturing process, a small increase in
CB content can lead to a large increase in the intensity of the CB odour .
18 of
I = Intensity of CB Odour
Kw = Constant based on how sensitive the human nose is at detecting odour from CB
CB0 = Cigarette butt content (%) to which 50% of the population can detect an odour (AMOL)
CB = Cigarette butt content.
1—Addition of whole CBs with no modification and Method 2—Addition of a concentrated CB pre-mix
(with a high % content of CB).
Like the automatic manufacturing process, once CBs have been delivered on-site, they will be
stored, cleaned, and handled strictly according to OH&S requirements.
4.2.4. Odour Issues and Reduction Methods for the Manual Process
As stated before, odour can be an issue in the production and use of CB bricks. In the manual
process, odour is a problem in the moulding and drying stages (stages 3–4) . The drying stage,
which could last for up to two weeks, takes place in an open environment where the sun has access to
the moulds. Gradually introducing CBs in the brick making process and assessing for AMOL would
be an ideal low-cost solution. This is considering that the bricks would be placed in an open air
environment, where the odour can be carried away by the air currents. However, if the
environment is densely populated, the CBs should be treated using effective UV light or other
methods before manufacturing. If UV treatment cannot be used, it is not recommended that CBs be
incorporated into the manual brick making process.
Figure 7. Typical CB Receptacles: free standing (top) and post mounted (bottom).
It is suggested that these companies deliver CBs (after appropriate preparations) directly to
the brick manufacturing facilities, instead of landfill or incineration sites. The advantages of delivering
CBs directly to brick manufactures are as follows: firstly, collection companies can save large amounts
of money by not having to pay for incineration or landfill of CB waste. Secondly, the negative
environmental effects of incineration and landfill can be avoided. Finally, brick manufacturers can gain
access to existing collection systems without having to pay for services or having to implement
their own collection schemes. However, it should be noted that, upon wide-scale introduction into
bricks, CBs may be considered to be a valuable source of energy, and, when demand is su fficient,
collection companies may decide to charge brick manufacturers for delivery. The safe storage and
handling of used CBs on-site are discussed in the following section of this paper.
Figure 8. CB samples utilised for preliminary bacteriological study 1. The dates indicate when the used
samples were collected in 2017.
The CBs used for this investigation were collected from the tops of bins around Victoria’s
Melbourne Central Station. Collecting CBs from the bins increased the chances that the samples
were fresh. Melbourne Central Station is a central hub for travel in Melbourne’s CBD and, therefore,
it provides reasonably representative samples (i.e., people from many areas and socio-economic
backgrounds travel through this area).
In this preliminary bacteriological investigation, the presence of Salmonella spp., Escherichia coli,
Pseudomonas aeruginosa, Enterococcus faecalis, Coagulase + ve Staphylococcus spp., and Streptococcus spp.
were investigated.
Escherichia coli live naturally in the intestinal tract of humans and animals and, in most cases,
is harmless [51]. However, some E. coli are pathogenic and they can cause diarrhoea or other illnesses
[51]. Although the most vulnerable include the elderly and young children, anyone can be
infected. The bacteria can be spread through contact with unclean surfaces that are contaminated
with faecal matter, such as human hands or door handles [51], and infections start when this bacteria is
consumed. As a result, it is possible that E. coli can be spread to CBs from unwashed hands that have
encountered contaminated surfaces, or they may even be present within the mouth when
contaminated food is consumed. Thus, the presence of E. coli was investigated.
Salmonella spp. commonly causes gastro, and it is spread through the ingestion of improperly
cooked food, water, or through hands that have encountered animal faeces [52]. As a result, it is
plausible that Salmonella spp. could be present on used CBs if smokers have not washed their
hands after coming into contact with animals, another infected person, or a contaminated material,
such as improperly cooked food. As this bacterium enters the body through the consumption of
contaminated food, it is also possible that it is present within the mouth.
Pseudomonas aeruginosa is primarily responsible for the infection of humans by Pseudomonas
strains of bacteria. Healthy people who are infected generally only present mild symptoms, but
those with
23 of
a weak immune system (such as those who are already sick) can suffer severe infections that can
be fatal. Pseudomonas aeruginosa can cause ear infections, eye infections, and skin rashes in healthy
people, whilst people with a weak immune system may contract blood infections and pneumonia
[53]. It is primarily spread by hand or from contact with contaminated equipment. Pseudomonas
aeruginosa thrives in moist environments.
Most Enterococcus species are not pathogenic and they are naturally found in the intestinal tract of
humans and animals. However, some strains, including Enterococcus faecalis, are known pathogens
that can cause several illnesses, including urinary tract infections and infections of open wounds.
Enterococcus species are difficult to kill, because they have developed a resistance to antibiotics,
including penicillin [54]. From the intestinal tract, Enterococcus species could spread to surfaces,
and hands, resulting in contamination, where it can be distributed through direct contact (WA n.d.).
It is entirely possible that these bacteria could be spread to the surface of CBs through
contaminated hands, hence it was investigated.
Staphylococcus bacteria are found naturally on the skin and in/around the nose (Healthdirect 2018).
It is estimated that around one-third of humans carry Staphylococcus [55]. In most cases these bacteria
cause no harm, but can become pathogenic if they enter the body. Its population growth can result in an
infection. Serious issues include skin impetigo, wound infection, cellulitis, pneumonia, septic arthritis,
sepsis, and endocarditis [56]. Some strains are particularly dangerous, as they are resistant to antibiotics.
It is likely that contact with the skin around the mouth or the hands of people that have touched their
nose could result in the contamination of CBs by Staphylococcus bacteria. As contaminated food enters
the body, Staphylococcus bacteria may also be present in the mouth, which may be transferred to CBs.
Streptococcus bacteria are found in the upper respiratory tract and skin of humans. There are
two types, Group A and Group B. Group A can cause the common ‘strep throat’, in addition to other
illnesses, such as scarlet fever, impetigo, and cellulitis. Group B can cause blood infections, pneumonia,
and meningitis [57]. The bacteria can be spread from person-to-person through sneezing and contact
with contaminated surfaces. As a result, it was determined that these bacteria could be present on
used CBs.
The results presented in Table 3 show that Coagulase + ve Staphylococcus spp. were sufficient
in number in sample 2, whilst there were insufficient numbers to be detected in sample 1. The presence
of Coagulase + ve Staphylococcus is shown in Figure 9.
Table 3. Preliminary bacteriological test results for used and unused CBs (Pilot investigation 1).
Coagulase + ve
SalMonella spp. Escherichia coli PseudoMonas aeruginosa Enterococcus spp. Streptococcus spp.
Sample Staphylococcus spp.
/15g MPN/g MPN/g MPN/g cfu/g
(unused CBs)
Note: the number of CBs in each sample were: control (75), sample 1 (72), sample 2 (71).
This bacterium was not detected in sample 1, which could be an indication that Staphylococcus
bacteria struggle to survive on CBs for an extended period. Alternatively, it could indicate that
Staphylococcus was only present on the CBs of sample 2. Despite the confirmation of the presence of
these bacteria, it has been reported that Staphylococcus requires a colony count exceeding 100,000 to
infect humans [58]. However, it is possible that these bacteria could enter via the mouth or through cuts
in the hands of workers, where the colony could flourish to an infectious concentration. Consequently,
it is recommended that gloves should be used when handling CBs.
24 of
A very small concentration of Enterococcus faecalis was also detected in sample 1, which reinforces
the prediction that unclean hands can transfer intestinal bacteria to CBs. It is possible that the original
concentration was higher, and the bacteria had slowly died over time. It is also plausible that the
original concentration was just as low and the bacteria can effectively survive on the surface of the
CBs for a few hours. In either case, the concentration is a negligible one, but it shows that the
bacteria are capable of surviving on the surface of used CBs for an unknown period.
Similar to the pilot investigation 1, the control group for pilot investigation 2 was prepared while
using the same method and preparations. The sample size was approximately double when compared
25 of
to investigation 1, as more tests were required to investigate the larger variety of bacteria. The control
group was prepared a day before the test.
For sample 1, fresh CBs for this investigation were collected from the tops of bins and their tilt
trays as well as ashtrays from restaurants/cafes around Melbourne’s CBD. Fresh CBs were collected
in this manner in order to reduce the chance of the butts being very old and the chance that the butts
encountered the ground. The samples were collected on the day before the testing. For sample 2, old
CBs that were a few months old were collected from RMIT University storage. Sample 3 comprised
old CBs that were a few months old and collected from RMIT storage; however, these CBs were placed
in an oven at 105 degrees for 6 h. Sample 4 were fresh CBs that were collected in the same manner as
sample 1, but had been treated with mothballs. The treatment consisted of placing two naphthalene
(mothballs) balls inside a bag full of CBs and leaving for 24 h before removing them from the bag for
testing. Samples 3 and 4 were two of the tested treatment methods for reducing the bacterium counts.
In this preliminary bacteriological investigation, the previous six bacteria were investigated:
Salmonella spp., Escherichia coli, Pseudomonas aeruginosa, Enterococcus faecalis, Coagulase + ve
Staphylococcus spp., and Streptococcus spp. Furthermore, an additional four types of bacteria were
investigated: Listeria spp., Legionella spp., Bacillus spp., and Clostridia spp.
Listeria spp. are present in a wide variety of environments, including the soil, in animals,
and in areas with water [59]. Most of the species of this bacteria group are not pathogens; however,
there is one pathogen within this species that is harmful to humans, the ‘Listeria monocytogenes’
[59]. This pathogen is harmful, as it can cause listeriosis. Although most healthy people who are
infected generally only present mild symptoms, it can prove fatal to people with a weak immune
system, the elderly, and can cause pregnant women to undergo a miscarriage [59]. L. monocytogenes can
exist and grow in food. Through consumption, L. monocytogenes may exist within the mouth, where
it is possible that it may spread to CBs. Therefore, the presence of this species has been
investigated.
Legionella spp. are naturally present in water sources of the environment. This pathogen is
harmful when it grows within artificial water systems, such as pipes, which are common within
households [60]. Legionella spp. can cause two main illnesses—pneumonia and Pontiac fever [60]. Most
healthy people who encounter Legionella spp. are not affected. Those vulnerable include the elderly,
smokers, and people with a weak immune system. Legionella spp. can enter the body via respiration
and aspiration. It is possible that Legionella spp. may be present in the evaporated water that people can
breathe if a colony is large enough and is thriving within an artificial water system [60]. Though less
frequent, people may also get sick when drinking water contaminated with Legionella spp., as it could
accidentally enter the lung [60]. It is possible that this pathogen is spread to CBs when exposed to
a water environment and, thus, the presence of this species has been investigated.
Bacillus spp. are generally present in soil environments [61]. They are most commonly found
in raw vegetables, water, organic matter, dust, and some flora species; however, there have been
scenarios where Bacillus spp. was found in other types of food groups, such as meats and rice,
and in hospital environments [61]. Most of these species are non-pathogenic. When Bacillus spp.
contaminates food, it typically survives the cooking procedure and, as a result, food poisoning is likely
to occur upon consumption [62]. This can be prevented through proper food handling. Gastrointestinal
illness can develop if a high quantity of Bacillus spp. is consumed [62]. It is possible that Bacillus spp.
could spread to CBs when exposed to soil, contaminated hands, contaminated surfaces, or the mouth,
hence the presence of this species was investigated.
Clostridia spp. are mainly present in soil environments where organic matter exists [63].
Other locations include the sediments of aquatic environments, and the intestinal tract and normal
microbial flora of animals and humans [64]. Pathogenic species that are harmful to humans include, but
are not limited to, C. botulinum—which can cause food-borne botulism, C. tetani—which can cause
tetanus,
C. perfringens—which can cause wounds, surgical infections, gas gangrene, and food poisoning, and,
lastly, C. difficile—which can cause antibiotic-associated diarrhoea, colitis, and
pseudomembranous colitis [64]. An external method for Clostridia spp. to enter the body is
from the consumption of
26 of
improperly cooked and stored food, in particular, meat and improperly heated canned food [63].
It is possible that Clostridia spp. could spread to CBs when encountering soil, contaminated hands,
contaminated surfaces, or the mouth; hence, the presence of this species was investigated.
The results presented in Table 4 show that Salmonella spp., E.coli, Coagulase + ve Staphylococcus
spp., Clostridia spp., and Legionella spp. were not found in any of the samples.
The investigation of Coagulase + ve Staphylococcus spp. for sample 1 (the freshest CBs of this
investigation) was not present in comparison to pilot investigation 1, where it was present in sample 2
(the fresh CBs of that investigation). This could be, because the sample was slightly fresher or that
the bacteria were only present within the sample collected. In this investigation, a small count of
Pseudomonas aeruginosa was found in sample 1. As this species of bacteria is primarily spread by
hand, its presence may be due to unclean hands that transfer the bacteria to CBs. A small count of
Enterococcus faecalis was found in the control sample, which was likely contaminated by the preparation
environment, as this bacterium was not present in the control sample of pilot investigation 1.
In sample 2, Listeria spp. was detected from the older CBs. Listeria spp. is known to survive
in waste water and sewerage sludge for a long period of time [65]. This sample may have been
contaminated by this species of bacteria, where its characteristics of surviving for a long period of time
can be observed.
Lastly, for Bacillus spp., counts of 70,000 cfu/g were found on control sample 1, 39,000 cfu/g
were found on sample 2, and 440 cfu/g were found on sample 3 (Figure 11). These higher
quantities are not unusual for soil. As Bacillus spp. have been recorded to grow on fresh and cured
tobacco leaves, this could be a plausible reason for its presence [66]. When comparing the dried
CBs from sample 3 with the other samples, the count of Bacillus spp. was significantly lower. This
indicates that the majority of Bacillus spp. that were present did not survive the drying process. It
was noted that sample 4Js preparation method was easier than sample 3 Js and it was almost as
effective at eliminating the Bacillus spp., counts.
Table 4. Preliminary bacteriological test results for used, unused, and dried used CBs and CBs with mothballs (Pilot investigation 2).
Coagulase + ve Total
SalMonella spp. Escherichia coli PseudoMonas aeruginosa Enterococcus spp. Streptococcus Listeria spp. Bacillus spp. Clostridia spp.
Staphylococcus
Samplespp. Leginella spp.
/15g MPN/g MPN/g MPN/g spp. cfu/g /25g cfu/g /g
cfu/g cfu/g
Control
Not Detected <2 <2 4 <100 <100 Not Detected 70,000 Not Detected <1000
(unused CBs)
Sample 1 Not Detected <2 2 <2 <100 <100 Not Detected 70,000 Not Detected <1000
Sample 2
Not Detected <2 <2 <2 <100 <100 Detected 39,000 Not Detected <1000
Stored CBs
Sample 3
Not Detected <2 <2 <2 <100 <100 Not Detected 440 Not Detected <1000
Dried CBs
Sample 4
Not Detected <2 <2 <2 <100 <100 Not Detected 4100 Not Detected <1000
with Mothballs
22 of
The workers dealing with cigarette butts should wear the appropriate PPE and follow OH&S
procedures to mitigate the potential risk that the pathogens and chemicals in CBs pose. Some of
the PPE recommended include wearing long sleeves and gloves and the use of an appropriate mask.
The results of both pilot investigations 1 and 2 should in no way be interpreted as a comprehensive
study. Only six types of bacteria were investigated for pilot investigation 1 and 10 types were
investigated for pilot investigation 2. In addition, only a small number of cigarettes were tested. About
75 CBs were collected for each sample for pilot investigation 1, and 150 CBs were collected for each
sample for pilot investigation 2. This quantity was then divided to investigate each species of bacteria,
thus limiting the scope of the findings.
This paper suggests that further investigation be conducted in this area, particularly given the
positive confirmation that Enterococcus faecalis, Coagulase + ve Staphylococcus spp., Pseudomonas
aeruginosa, Listeria spp., and Bacillus spp. were present in such a small population of CBs.
Attempts at determining a way of investigating the presence of viruses failed, as it is impractical
to develop a method to utilise for testing and almost impossible to verify whether the produced results
would be accurate, or that the virus presented a viable infectious threat.
5.3.1. Naphthalene
Naphthalene is a white crystalline powder that produces a well-recognised smell (mothballs).
The chemical is isolated from coal tar and has a relatively short half-life in the atmosphere of 3–8 h [ 71].
Naphthalene is the major active ingredient in ‘toilet cakes’, and it is used as a fumigant [72].
Naphthalene is a suspected carcinogen, and exposure to very high concentrations can lead to damage to
blood cells and haemolytic anaemia. However, exposure to low concentrations in the open air
should be safe for adults and children older than 3 [73]. Naphthalene and its derivatives have proven
antimicrobial capacities [74]. In addition, a common dye, β-naphthol, possesses effective antimicrobial
properties [75]. Mkpenie et al. (2008) confirmed this, testing azo-2 naphthol and 2-naphthol on five
pathogenic microorganisms: Escherichia coli, Staphylococcus aureus, Streptococcus faecalis, Pseudomonas
aeruginosa, and Bacillus subtilis [76]. The results demonstrated that both chemicals were highly effective
at killing all the microorganisms tested. When considering Naphthalene’s short half-life in the
atmosphere and antimicrobial abilities, in addition to the ease in which ‘mothballs’ and ‘toilet cakes’
can be located and purchased, these products are potentially a very quick, easy, and cheap method
for cleaning CBs, as seen in Section 6.2.2. This paper suggests that toilet cakes or mothballs could be
placed into the bags that dry CBs are collected in (i.e., by the collector) and tied. The fumigation effects
would then likely kill any possible bacteria. Care should be taken not to inhale the fumes that are
released when the bag
23 of
is opened, as per the reasons stated above. The fumes produced should be minimal if only a few toilet
cakes/mothballs are used. This method would be cheap, simple, and effective.
The following methods are more suitable for large scale-cleaning plants.
5.3.2. Ozone
Ozone (O3) is an unstable gas with powerful oxidising properties. It is predominately
produced naturally as a result of ultraviolet rays irradiating oxygen molecules in the stratosphere,
where up to 90% of all ozone is located [77]. Research has shown that ozone is an effective
antibacterial agent and that it is useful against both gram positive and gram-negative bacteria, as
well as spores and vegetative cells [78]. This antimicrobial power is predominately a result of the
oxidising potential of ozone, where molecular ozone or its decomposition products, such as radical
hydroxyl ions, react with bacteria/virus cells and disrupt normal functions, thereby resulting in
inactivation or destruction [79]. Ozone generators are widely available and, therefore, could be
considered to be easily accessible in most situations. Ozone has been used to sterilise equipment and
containers in the food industry for many years, including in Japan, where the method has been
utilised in food manufacturing facilities since 1982 [80]. Using ozone to sanitize surfaces,
equipment, and even food is quite safe, as, even though ozone is highly toxic, it quickly
disassociates into oxygen [81].
Ozone is effective as an antimicrobial due to its potent oxidisation capabilities [82]. The third
oxygen atom in ozone is only loosely bonded and, as a result, is unstable and highly reactive. It will
attach itself to organic matter, such as bacteria, and destroy them through the process of oxidisation
[83]. Ozone has also been shown to have a capacity to destroy a wide variety of viruses, including
hepatitis A and influenza A [84]. Treating fruits and vegetables with ozone has also been shown to
increase the shelf life of the products [85,86]. It is essential to remember that ozone is a toxic gas,
and it can be lethal in sufficiently high doses [87]. Therefore, it is essential that system designs ensure
that humans have no exposure to ozone.
Ozone sterilisation of surfaces can occur in two main forms: gaseous ozone and ozonated
water. Objects can be submerged in ozonated water for treatment or can be exposed to continuously
generated gas-phase ozone. Rooms can be sealed, whilst gaseous ozone is generated for sterilisation.
The ozone will decompose into oxygen atoms at a rate that is influenced by both room temperature and
the surface composition of any catalyst [88]. No personnel can be present inside a sealed room during
the gaseous ozone sterilisation process for the reasons stated above. A gaseous ozone concentration of
25 parts-per-million (ppm) in air at a Relative Humidity (RH) of 90% was found to be bactericidal after
an exposure time of 20 min. [81]. A large volume of research shows that ozone has substantial oxidising,
antibacterial, and antiviral capabilities, which suggests that it could be applied for the treatment of
any potential bacteria, viruses, and fungal spores on CBs. This paper suggests that gas phase ozone
is a more appropriate method when considering the need to control the moisture content of mixes,
and the relatively complex process of producing large volumes of ozonated water.
HO. Free radicals react with bacteria/virus cells and, thus, prevent the correct functioning of these cells.
This results in the inhibition of infection and replication processes [95]. An advantage of vaporised
hydrogen peroxide when compared to gaseous ozone is that it has relatively low toxicity to humans and
breaks down spontaneously into harmless components [92]. Vaporised hydrogen peroxide generation
systems are widely available. Hydrogen peroxide may be an effective treatment method for any viruses,
bacteria, or fungi that may be present on CBs as a result of its availability and sterilising properties.
The ignition temperature of paper has been reported to be in the range of 218–246 ◦C and,
therefore, under dry heat temperatures of 180 ◦C CBs would not be expected to combust [106].
However, great care must be ensured if dry heat sterilisation is utilised for the treatment of CBs, as the
presence of various chemicals may alter the ignition temperature.
It is essential to wear appropriate masks when handling dry CBs. This is to protect against any
possible inhalation of VOC or exposure to any pathogens that may be present in the sample, and it
is especially important in a brick factory due to the dust exposure alone. Hand protection is
required to ensure that pathogens do not enter cuts by chemicals getting absorbed through the skin. In
addition to this, it is very important to wear gloves when handling CBs that are moist, as heavy
metals, such as lead, cadmium, and arsenic, can leach off the butts.
It is recommended that CBs be sterilised immediately upon or prior to delivery to the
manufacturing site. Several appropriate methods have been discussed that have been deemed to be
suitable for industrial scale sterilisation of used CBs. For small volumes of CBs, the use of mothballs
or toilet cakes that contain Naphthalene can be cost efficient, as, when placed in the bag
containing CBs, the Naphthalene will fumigate all or some of the bacteria that may be present (further
investigation is recommended in this area). However, this solution is considered to be viable for
small volumes and should be used in the interim until a larger scale sterilisation method can be
implemented
Previous investigations into the leachates from manufactured CB bricks show that, after firing,
only trace amounts of metal leachates were found in bricks with 2.5, 5.0, 7.5, and 10.0% content of
CBs [23]. These concentrations were lower than the regulatory limits set by USEPA (1996) and
EPAV (2005) [33,34].
Odour from the incorporation of CBs into brick production should also be addressed.
The issue stems from VOCs being emitted from CBs and can either be addressed prior to entering
the manufacturing site or during manufacturing of CB bricks. It should be noted that odour disappears
after the firing of the bricks occurs.
As always, it is essential that local regulations and standards regarding the handling of municipal
waste be adhered to.
27 of
Implementation Guide
The following steps may be followed for the implementation
of recycling CBs in fired-clay bricks.
I. For CB collection, aim to develop a close relationship with
CB collection companies to facilitate the delivery of CBs to
manufacturing sites. These CBs are normally collected
from modern bins or receptacles.
II. Once the CBs are collected, a sterilisation method (Section 6)
should be used to clean the CBs from bacteria. The odour
may be purged from CBs in this stage (Section 5). If
mothballs (containing naphthalene) are used, they should be
put into the bags containing CBs to inactivate any bacteria
that may be present. This can be done by the collector or
by workers on-site. Care should be taken to not breathe in
fumes when the bags are opened. The CBs will then be
stored on-site.
III. When ready, CBs can be incorporated into the brick clay
mix through a method suggested in Section 5 for
incorporation into Automatic Processes and 5.2 for
incorporation into Manual Processes. Once the CBs have
been incorporated, the remaining steps that are common
within the brick manufacturing process can be followed.
IV. Always ensure that relevant OH&S standards are followed,
the correct PPE is worn, and the fumes are not breathed.
Refer to Section 5.1.4_5.1.4_Appropriate_PPE,
5.2.3_5.2.3_Appropriate_PPE, and 6.4_6.4._Safe_Handling
for more detail on the safe handling of CBs.
28 of
conclusions
This study has presented and discussed some of the results of an ongoing study on
recycling CBs in fired-clay bricks. The results of a CB energy contribution study,
bacteriological investigation of CBs, and the properties of bricks incorporating CBs have been
discussed. Additionally, the implementation procedure for recycling CBs in bricks and the pre-
processing issues of CBs are analysed and discussed. The main findings are summarised and
discussed below. Energy savings: the calorific value of CBs was investigated. It was found that
the average gross calorific value of CBs with remnant tobacco was 16.5 MJ/kg. This is a high
value when compared to the calorific value of black coal, which is 20 MJ/kg. If 2.5% of all the
bricks produced annually around the world include 1% CB content, the energy consumption
of the process can be reduced by over 20 billion MJ. This approximately equates to the power
used by one million homes every year in the State of Victoria, Australia. Therefore adding 1%
CBs (about 20 kg/m3) to the brick clay results in significant energy savings, solves the CB
pollution problem globally, and tangibly reduces the environmental impact of the brick
manufacturing industry, while concurrently providing financial savings to manufacturers
through the reduction in energy for firing bricks. Fired-clay bricks are excellent for recycling
waste materials. There is a need for a specially dedicated brick factory in every state/country
for recycling cigarette butts and other similar waste materials. Incorporation of large amounts
of CBs in fired clay bricks is not recommended due to the high calorific value of CBs.
Bacteriological investigations: a serious concern in the recycling of used CBs is that they
may be contaminated with bacteria or viruses from contact with people or the environment.
As a result, this study undertook two pilot investigations. The presence of ten common
bacteria was investigated on unused, fresh, and old CBs. In the first investigation, used CBs
that were one week old, and used CBs that were collected on the day of the testing day were
compared with an unused control sample. A small colony of Coagulase + ve Staphylococcus
spp. was detected on the same-day sample. For the second investigation, used CBs that were
collected a day before the testing, used old CBs, and used CBs dried at 105 degrees for 6 h were
tested and compared with the control sample. The most significant finding from this
investigation was that Listeria spp. was detected in the used old CB sample and that
all used and unused CB samples, except the dried sample, had significant counts of
Bacillus spp. It was
also found that the effect of the contact of naphthalene balls with fresh used CBs on the
reduction of Bacillus spp., bacteria, was very significant. This study suggests that naphthalene-
containing mothballs be used to fumigate bags that were used to collect and store CBs. Further
study is recommended in this area. Several suitable sterilisation methods have been reviewed
and discussed to address the potential for the presence of pathogens in CBs.
Sterilisation methods: Following the two bacteriological investigations, several industrial
sterilisation measures have been studied, including ozone, vaporized hydrogen peroxide,
moist heat sterilisation, and dry heat sterilisation, Ultraviolet Light Radiation (UV), and
Naphthalene. These methods could be employed to sterilise large volumes of waste materials.
29 of
Hydrogen peroxide may be an effective and practical sterilising method for any viruses,
bacteria, or fungi that may be present on CBs for large scale-cleaning plants.
Properties of bricks incorporating CBs: the compressive strength of 1% CB content bricks
with 15.5% and 17.5% moisture content averaged 27.5 MPa and 25.8 MPa, respectively, down
from the 43.2 MPa exhibited by the 15% moisture content control bricks. The standard
compressive strength for bricks for low-medium rise residential structures in Australia is
between 10 and 20 MPa. The decrease in compressive strength as a result of the increase in CB
content, establishes a limitation regarding
the content of CB that can be incorporated in fired clay bricks. The dry density of the
bricks decreased from 2134 kg m−3 to 1964 kg m−3 (8% reduction). This results in bricks
with lower thermal conductivity, which are lighter and therefore reduce the ‘dead-weight’ of
potential structures. Lower thermal conductivity can have a significant influence on the energy
consumption of a home, as it reduces
the need to use air-conditioning systems to adjust the temperature inside the house. The
water absorption and initial rate of absorption of the brick increased as expected, due to the
reduction in density of the samples. However, the changes were minor and well within
acceptable limits. These results confirm the previous results that were published by
Mohajerani et al. (2016).
Implementation procedures: three processing methods have been suggested to
incorporate the CBs into the automatic brick manufacturing process. Shredding CBs is
expected to improve uniformity in the particle size and distribution of CBs within the mix,
thereby leading to clay bricks with more uniform properties. However, the shredding of the
CBs must be performed in a fully
Proposal
Approximately six-trillion cigarette butts are littered worldwide
every year, resulting in over
1.2 million tonnes of toxic to highly toxic waste contaminating our
cities and the environment. Considering the combined risks from
hundreds of highly toxic chemicals and possible pathogens in
cigarette butts, it is proposed that the littering of this waste anywhere in
cities and the environment be strictly prohibited, and that offenders be
heavily fined. This strategy should be supported by appropriate
education, guidelines, and advertising. Our cities, parks, waterways,
beaches, and oceans have been contaminated for many years, with
millions of tonnes of unsightly and toxic cigarette butts. Effective and
strong laws and guidelines by governments for solving this global
pollution problem are overdue and urgently need to be established.
This action should be supported by an adequate number of receptacles
installed at critical locations in cities and public places by local
governments for the collection of CBs for recycling. The sincere,
effective, and urgent support and cooperation of smokers,
governments, educators, and waste management industries are
essential for ending the littering of cigarette butts in the environment.
Abbreviations
References
1. The Tobacco Atlas. ‘Consumption’, American Cancer Society. 2018. Available online:
https://tobaccoatlas. org/topic/consumption/ (accessed on 18 December 2019).
2. Carlozo, L.R. ‘Kicking Butts’, Chicago Tribune. 2018. Available online:
http://www.chicagotribune.com/ news/ct-xpm-2008-06-18-0806170174-story.html (accessed
on 27 March 2019).
3. Keep Australia Beautiful. Cigarette Butts. 2017. Available online:
http://www.kabc.wa.gov.au/report- littering/cigarette-butts (accessed on 17 November 2019
4.
World Health Organization. Tobacco and Its Environmental Impact: An Overview; World Health Organization:
Geneva, Switzerland, 2017.
1. Mackay, J.; Eriksen, M.; Eriksen, M.P. The Tobacco Atlas; World Health Organization: Geneva,
Switzerland, 2002.
2. Srbinoska, M.; Radojicˇic´, V.; Ðulancˇic´, N.; Kirkova, S. Possibilities for managing the cigarette butts
waste. In Proceedings of the 26th International Conference Ecological Truth & Environmental Research, Bor
Lake, Serbia, 12–15 June 2018.
3. Hoffmann, D.H.I. The Changing Cigarette, 1950–1995. J. Toxicol. Environ. Health 1997, 50, 307–
364. [CrossRef] [PubMed]
4. Australian Government. Cigarettes and Poison. 2013. Available online:
http://www.quitnow.gov.au/internet/ quitnow/publishing.nsf/Content/cigarettes-and-poison (accessed on 6
October 2019).
5. Hecht, S.S. Research Opportunities Related to Establishing Standards for Tobacco Products Under
the Family Smoking Prevention and Tobacco Control Act. Nicotine Tob. Res. 2012, 14, 18–28. [CrossRef]
[PubMed]
6. Hoffmann, D.; Hoffmann, I.; El-Bayoumy, K. The less harmful cigarette: A controversial issue. A
tribute to Ernst L. Wynder. Chem. Res. Toxicol. 2001, 14, 767–790. [CrossRef] [PubMed]
7. Hoffmann, D.; Djordjevic, M.V.; Brunnemann, K.D. Changes in cigarette design and composition
over time and how they influence the yields of smoke constituents. J. Smok. Relat. Disord 1995, 6, 9–23.
8. Hon, N.-S. Photodegradation of cellulose acetate fibers. J. Polym. Sci. A Polym. Chem. 1977, 15, 725–
744. [CrossRef]
9. Dieng, H.; Rajasaygar, S.; Ahmad, A.H.; Ahmad, H.; Rawi, C.S.M.; Zuharah, W.F.; Satho, T.; Miake, F.;
Fukumitsu, Y.; Saad, A.R.; et al. Turning cigarette butt waste into an alternative control tool against an
insecticide-resistant mosquito vector. Acta Trop. 2013, 128, 584–590. [CrossRef] [PubMed]
10. Marinello, S.; Lolli, F.; Gamberini, R.; Rimini, B. A second life for cigarette butts? A review of
recycling solutions. J. Hazard. Mater. 2019, 384, 121–245. [CrossRef]
11. Micevska, T.; Warne, M.; Pablo, F.; Patra, R. ariation in, and causes of, toxicity of cigarette butts to a
cladoceran and microtox. Arch. Environ. Contam. Toxicol. 2006, 50, 205–212. [CrossRef]
12. Slaughter, E.; Gersberg, R.M.; Watanabe, K.; Rudolph, J.; Stransky, C.; Novotny, T.E. Toxicity of
cigarette butts, and their chemical components, to marine and freshwater fish. Tob. Control 2011, 20 (Suppl. 1),
i25–i29. [CrossRef]
13. Rebischung, F.; Chabot, L.; Biaudet, H.; Pandard, P. Cigarette butts: A small but hazardous waste,
according to European regulation. Waste Manag. 2018, 82, 9–14. [CrossRef]
14. Clean Up Australia Report. 2017. Available online: https://www.cleanup.org.au/rubbish-report
(accessed on 1 September 2019).
15. Torkashvand, J.; Farzadkia, M. A systematic review on cigarette butt management as a hazardous
waste and prevalent litter: Control and recycling. Environ. Sci. Pollut. Res. 2019, 26, 11618–11630. [CrossRef]
[PubMed]
16. Kurmus, H.; Mohajerani, A. The toxicity and valorization options of cigarette butts. Waste Manag.
2020, 104,
104–118. [CrossRef] [PubMed]
33 of
17. Kurmus, H.; Mohajerani, A. Leachate Analysis of Heavy Metals in Cigarette Butts and Bricks
Incorporated with Cigarette Butts. Materials 2020, 13, 2843. [CrossRef] [PubMed]
18. Mohajerani, A.; Tanriverdi, Y.; Nguyen, B.T.; Wong, K.K.; Dissanayake, H.N.; Johnson, L.; Whitfield,
D.; Thomson, G.; Alqattan, E.; Rezaei, A. Physico-mechanical properties of asphalt concrete incorporated with
encapsulated cigarette butts. Constr. Build. Mater. 2017, 153, 69–80. [CrossRef]
19. Mohajerani, A.; Kadir, A.A.; Larobina, L. A practical proposal for solving the world’s cigarette butt
problem: Recycling in fired clay bricks. Waste Manag. 2016, 52, 228–244. [CrossRef]
20. Neil, J.; Ravinda, K.D. Civil Engineering Materials, 5th ed; Macmillan Education Press: London, UK,
1997.
21. Muñ oz Velasco, P.; Morales Ortíz, M.P.; Mendívil Giró , M.A.; Muñ oz Velasco, L. Fired clay bricks
manufactured by adding wastes as sustainable construction material—A review. Constr. Build. Mater. 2014, 63,
97–107. [CrossRef]
22. Prasertsan, S. Preliminary Study on Brick Making Industry in ASEAN Countries. In Final Report
(Unpublished);
NRCT: Bangkok, Thailand, 1995.
23. Australian Standard. AS/NZS 1289.5.1.1. Method 5.1.1. In Methods for Testing Soils for
Engineering Purposes—Soil Compaction and Density Tests—Determination of the Dry Density/Moisture
Content Relations of a Soil Using Standard Compactive Effort; SAI Global: Standards Australia: Sydney,
Australia, 2003.
24. Sutcu, M.; Akkurt, S. AS/NZS 4456.1:2008 (Masonry Units and Segmental Pavers and Flags, 2008);
SAI Global: Standards Australia: Sydney, Australia, 2008.
25. Eliche-Quesada, D.; Martínez-Martínez, S.; Pérez-Villarejo, L.; Iglesias-Godino, F.J.; Martínez-García
CCorpas-Iglesias, F.A. Valorization of biodiesel production residues in making porous clay brick. Fuel
Process. Technol. 2012, 103, 166–173. [CrossRef]
26. Sutcu, M.; Akkurt, S. The use of recycled paper processing residues in making porous brick with
reduced thermal conductivity. Ceram. Int. 2009, 35, 2625–2631. [CrossRef]
27. Kadir, A.A.; Mohajerani, A. Possible utilization of cigarette butts in light-weight fired clay bricks.
Int. J. Civ.
Environ. Eng. 2008, 2, 137–141.
28. Kadir, A.A.; Mohajerani, A. Recycling cigarette butts in lightweight fired clay bricks. Constr. Mater.
2011,
164, 219–229. [CrossRef]
29. USEPA. Hazardous Waste Characteristics Scoping Study; Office of Solid Waste; US Environmental
Protection Agency: Washington, DC, USA, 1996.
30. EPAV. Guidelines for Hazard Classification of Solid Prescribed Industrial Waste; Environmental
Protection Agency of Victoria: Melbourne, Australia, 2005.
31. Midwest Research Institute (MRI). Brick and Structural Clay Product Manufacturing; United States
Environmental Protection Agency: Washington, DC, USA, 1997.
32. Mortar Industry Association (MIA). Brick and Block Production; Mortar Industry Association:
London, UK, 2013.
33. Ibstock Brick Ltd. How Clay Bricks Are Made; Ibstock: Leicestershire, UK, 2005; Available online:
https:
//www.ibstockbrick.co.uk/wp-content/uploads/2015/08/TIS-A1-HOW-BRICKS-ARE-MADE-3.pdf (accessed
on 4 October 2019).
34. Africa Clay Brick Association of South. Clay Brick Technical Guide; ABC Press: Cape Town, South
Africa, 2015.
35. Brick Industry Association. Technical Notes on Brick Construction; The Brick Industry Association:
Reston, VA, USA, 2006.
36. Alternatives Development. Enabling Policies in the Indian Brick Sector-Current Status and Future
Trends; Alternatives Development: New Delhi, India, 2012.
37. Jrup, L. Hazards of heavy metal contamination. Br. Med. Bull. 2003, 68, 167–182. [CrossRef]
34 of
[PubMed]
38. Charles, S.M.; Batterman, S.A.; Jia, C. Composition and emissions of VOCs in main- and side-stream
smoke of research cigarettes. Atmos. Environ. 2007, 41, 5371–5384. [CrossRef]
39. Martuzevicius, D.; Prasauskas, T.; Setyan, A.; O’connell, G.; Cahours, X.; Julien, R.; Colard, S.
Characterization of the Spatial and Temporal Dispersion Differences Between Exhaled E-Cigarette Mist and
Cigarette Smoke. Nicotine Tob. Res. 2019. [CrossRef] [PubMed]
40. Poppendieck, D.; Khurshid, S.; Emmerich, S. Measuring Airborne Emissions from Cigarette Butts:
Literature
Review and Experimental Plan; National Institute of Standards and technology U.S Department of commerce:
Gaithersburg, MA, USA, 2016.
41. Sherman, C.; Weaver, E. The Senses: Smell and Taste’, The Dana Alliance for Brain Initiatives. 2016.
Available online: https://www.dana.org/uploadedFiles/Pdfs/Brain-Brief-Senses-Smell-and-Taste-FINAL.pdf
(accessed on 14 November 2019).
42. Encyclopædia Britannica. 2018. Available online: https://www.britannica.com/science/methane
(accessed on 1 October 2019).
43. Miljøstyrelsen, V.F. Industrial Odour Control; Agency, D.E.P., Ed.; Danish Minestry of the
Enviroment:
Copenhagen, Denmark, 2002; p. 29.
44. Laliberte, G. What is the Difference between Odour Concentration and Odour Intensity for
Regulators? Available online: http://www.odotech.com/en/odour_concentration_vs_intensity/ (accessed on 16
October 2019).
45. Normand Brais. ‘Garbage Room Odors Remediation’, Sanuvox. 2017. Available online:
https://sanuvox. com/wp-content/uploads/2019/04/OdorControl_EN.pdf (accessed on 15 December 2019).
46. City of Melbourne. Cigarette Butt Disposal. 2018. Available online:
https://www.melbourne.vic.gov.au/ business/waste-recycling/Pages/cigarette-butt-disposal.aspx (accessed
on 5 October 2019).
47. Centers for Disease Control and Prevention. E. coli (Escherichia coli). 2018. Available online:
https:
//www.cdc.gov/ecoli/general/index.html (accessed on 4 October 2019).
48. SA Health. Salmonella Infection—Including Symptoms, Treatment and Prevention. 2017. Available
online: https://www.sahealth.sa.gov.au/wps/wcm/connect/public+content/sa+health+internet/
health+topics/ health+conditions+prevention+and+treatment/infectious+diseases/salmonella+infection/
salmonella+ infection+-+including+symptoms+treatment+and+prevention (accessed on 4 October 2019).
49. Centers for Disease Control and Prevention. Pseudomonas aeruginosa in Healthcare Settings. 2018.
Available online: https://www.cdc.gov/hai/organisms/pseudomonas.html (accessed on 4 October 2019).
50. Fraser, S.L. Enterococcal Infections. 2018. Available online:
https://emedicine.medscape.com/article/216993- overview#a4 (accessed on 4 October 2019).
51. Centers for Disease Control and Prevention. Staphylococcus aureus in Healthcare Settings. 2011.
Available online: https://www.cdc.gov/hai/organisms/staph.html (accessed on 4 October 2019).
52. Healthdirect. Staph Infections. 2018. Available online: https://www.healthdirect.gov.au/staph-
infections (accessed on 4 October 2019).
53. MedlinePlus. Streptococcal Infections. 2018. Available online:
https://medlineplus.gov/streptococcalinfections. html (accessed on 4 October 2019).
54. Schmid-Hempel, P.; Frank, S.A. Pathogenesis, virulence, and infective dose. PLoS Pathog. 2007, 3,
e147.
[CrossRef] [PubMed]
55. Food Standards Australia New Zealand 2013. Listeria Monocytogenes; Food Standards Australia
New Zealand: Sydney, Australia, 2013.
56. Centers for Disease Control and Prevention. Legionella (Legionnaires’ Disease and Pontiac Fever).
2018. Available online: https://www.cdc.gov/legionella/about/causes-transmission.html (accessed on 4
October 2019).
35 of
75. Khadre, M.; Yousef, A.; Kim, J.G. Microbiological aspects of ozone applications in food: A review. J.
Food Sci.
2001, 66, 1242–1252. [CrossRef]
76. Naitou, S.; Takahara, H. Recent Developments in Food and Agricultural uses of Ozone as an
36 of
Antimicrobial Agent-Food Packaging Film Sterilizing Machine using Ozone. Ozone Sci. Eng. 2008, 30, 81–87.
[CrossRef]
77. Sharma, M.; Hudson, J.B. Ozone gas is an effective and practical antibacterial agent. Am. J. Infect.
Control
2008, 36, 559–563. [CrossRef] [PubMed]
78. Greene, A.K.; Few, B.K.; Serafini, J.C. A Comparison of Ozonation and Chlorination for the
Disinfection of Stainless Steel Surfaces. J. Dairy Sci. 1993, 76, 3617–3620. [CrossRef]
79. Ozone Oxidation is Nature’s Sanitation Powerhouse. 2017. Available online:
http://www.delozone.com/ ozone-technology/about-ozone.php (accessed on 11 October 2019).
80. Burleson, G.R.; Murray, T.; Pollard, M. Inactivation of viruses and bacteria by ozone, with and
without sonication. Appl. Microbiol. 1975, 29, 340–344. [CrossRef] [PubMed]
81. Norton, J.; Charig, A.; Demoranville, I. Effect of ozone on storage of cranberries. In Proceedings of
the American
Society for Horticultural Science; American Society for Horticultural Science: Alexandria, VA, USA, 1968;
Volume 93, p. 792.
82. Rice, R.G.; Farquhar, J.W.; Bollyky, L.J. Review of the applications of ozone for increasing storage
times of perishable foods. Ozone Sci. Eng. 1982, 4, 147–163.
83. Hoof, F. Professional risks associated with ozone. Ozonation Man. Water Waste Water Treat. 1982,
200–201.
84. Batakliev, T.; Georgiev, V.; Anachkov, M.; Rakovsky, S.; Zaikov, G.E. Ozone decomposition.
Interdiscip. Toxicol.
2014, 7, 47–59. [CrossRef] [PubMed]
85. National Center for Biotechnology Information. ‘Hydrogen Peroxide’, PubChem Compound
Database; CID=784. 2004. Available online: https://pubchem.ncbi.nlm.nih.gov/compound/hydrogen_peroxide
(accessed on 11 September 2019).
86. Chung, S.; Kern, R.; Koukol, R.; Barengoltz, J.; Cash, H. Vapor hydrogen peroxide as alternative to
dry heat microbial reduction. Adv. Space Res. 2008, 42, 1150–1160. [CrossRef]
87. Fu, T.Y.; Gent, P.; Kumar, V. Efficacy, efficiency and safety aspects of hydrogen peroxide vapour and
aerosolized hydrogen peroxide room disinfection systems. J. Hosp. Infect. 2012, 80, 199–205. [CrossRef]
88. Linley, E.; Denyer, S.P.; McDonnell, G.; Simons, C.; Maillard, J.Y. Use of hydrogen peroxide as a
biocide: New consideration of its mechanisms of biocidal action. J. Antimicrob. Chemother. 2012, 67, 1589–
1596. [CrossRef]
89. Kahnert, A.; Seiler, P.; Stein, M.; Aze, B.; McDonnell, G.; Kaufmann, S.H. Decontamination with
vaporized hydrogen peroxide is effective against Mycobacterium tuberculosis. Lett. Appl. Microbiol. 2005, 40,
448–452. [CrossRef] [PubMed]
90. Fichet, G.; Antloga, K.; Comoy, E.; Deslys, J.; McDonnell, G. Prion inactivation using a new gaseous
hydrogen peroxide sterilisation process. J. Hosp. Infect. 2007, 67, 278–286. [CrossRef] [PubMed]
91. Pottage, T.; Richardson, C.; Parks, S.; Walker, J.T.; Bennett, A.M. Evaluation of hydrogen peroxide
gaseous disinfection systems to decontaminate viruses. J. Hosp. Infect. 2010, 74, 55–61. [CrossRef]
92. Bintsis, T.; Litopoulou-Tzanetaki, E.; Robinson, R.K. Existing and potential applications of
ultraviolet light in the food industry–a critical review. J. Sci. Food Agric. 2000, 80, 637–645. [CrossRef]
93. Rock, C.; Curless, M.S.; Nowakowski, E.; Ross, T.; Carson, K.A.; Trexler, P.; Carroll, K.; Maragakis, L.L.
UV-C Light Disinfection of Carbapenem-Resistant Enterobacteriaceae from High-Touch Surfaces in a Patient
Room and Bathroom. Infect. Control Hosp. Epidemiol. 2016, 37, 996–997. [CrossRef] [PubMed]
94. Bae, Y.M.; Lee, S.Y. Inhibitory Effects of UV Treatment and a Combination of UV and Dry Heat
against Pathogens on Stainless Steel and Polypropylene Surfaces. J. Food Sci. 2012, 77, M61–M64. [CrossRef]
95. Cutler, T.D.; Zimmerman, J.J. Ultraviolet irradiation and the mechanisms underlying its inactivation
of infectious agents. Anim. Health Res. Rev. 2011, 12, 15–23. [CrossRef]
96. Jagger, J. Introduction to Research in Ultra-Violet Photobiology; Prentice-Hall: Englewood Cliffs, NJ,
USA, 1967.
97. Petersson, L.P.; Albrecht, U.-V.; Sedlacek, L.; Gemein, S.; Gebel, J.; Vonberg, R.-P. Portable UV light as
an alternative for decontamination. Am. J. Infect. Control 2014, 42, 1334–1336. [CrossRef]
37 of
98. Angela, T.; Robert, P.S.; Antony, R.Y. UVA1 Induces Cyclobutane Pyrimidine Dimers but Not 6-4
Photoproducts in Human Skin In Vivo. J. Investig. Dermatol. 2011. [CrossRef]
99. Mallet, J.D.; Rochette, P.J. Wavelength-dependent ultraviolet induction of cyclobutane pyrimidine
dimers in the human cornea. Photochem. Photobiol. Sci. 2013, 12, 1310–1318. [CrossRef]
100. Smelt, J.P.; Brul, S. Thermal inactivation of microorganisms. Crit. Rev. Food Sci. Nutr. 2014, 54,
1371–1385. [CrossRef] [PubMed]
101. Darmady, E.M.; Hughes, K.E.; Jones, J.D.; Prince, D.; Tuke, W. Sterilization by dry heat. J. Clin. Pathol.
1961,
14, 38. [CrossRef] [PubMed]
102. Cafe, T. Physical Constants for Investigators. Available online:
http://www.tcforensic.com.au/docs/article10. html#2.1 (accessed on 13 April 2019).
103. Pavia, C.S.; Pierre, A.; Nowakowski, J. Antimicrobial activity of nicotine against a spectrum of
bacterial and fungal pathogens. J. Med. Microbiol. 2000, 49, 675–676. [CrossRef] [PubMed]
104. Adeleye, I.; Onubogu, C.; Ayolabi, C.; Isawumi, A.; Nshiogu, M. Screening of crude extracts of twelve
medicinal plants and “wondercure” concoction used in Nigeria unorthodox medicine for activity against
mycobacterium tuberculosis isolated from tuberculosis patients sputum. Afr. J. Infect. Dis. 2008, 2, 2. [CrossRef]
105. Bakht, J.; Azra; Shafi, M. Antimicrobial activity of Nicotiana tabacum using different solvents
extracts.
Pak. J. Bot. 2012, 44, 459–463.
106. Stewart, G.G. A history of the medicinal use of tobacco 1492–1860. Med. Hist. 1967, 11, 228–268.
[CrossRef] [PubMed]
107. Charlton, A. Medicinal uses of tobacco in history. J. R. Soc. Med. 2004, 97, 292–296. [CrossRef]
108. Mayer, B. How much nicotine kills a human? Tracing back the generally accepted lethal dose to
dubious self-experiments in the nineteenth century. Arch. Toxicol. 2014, 88, 5–7. [CrossRef]
109. Zuskin, E.; Mustajbegovic, J.; Schachter, E.N.; Kern, J.; Doko-Jelinic, J.; Godnic-Cvar, J. Respiratory
findings in workers employed in the brick-manufacturing industry. J. Occup. Environ. Med. 1998, 40, 814–820.
[CrossRef]
110. Myers, J.E.; Cornell, J.E. Respiratory health of brickworkers in Cape Town, South Africa: Symptoms,
signs and pulmonary function abnormalities. Scand. J. Work Environ. Health 1989, 15, 188–194. [CrossRef]
111. Raza, A.; Qamer, M.; Afsheen, S.; Adnan, M.; Naeem, S.; Atiq, M. Particulate Matter Associated Lung
Function Decline in Brick Kiln Workers of Jalalpur Jattan, Pakistan. Pak. J. Zool. 2014, 46, 237–243.
112. Sanjel, S.; Khanal, S.N.; Thygerson, S.M.; Carter, W.S.; Johnston, J.D.; Joshi, S.K. Respiratory
symptoms and illnesses related to the concentration of airborne particulate matter among brick kiln workers
in Kathmandu valley, Nepal. Ann. Occup. Environ. Med. 2017, 29. [CrossRef] [PubMed]
113. Fishwick, D.; Sumner, J.; Barber, C.M.; Robinson, E.; Codling, A.; Lewis, L.; Young, C.; Warren, N. P61
Respiratory ill health in the silica exposed brick manufacturing sector. Thorax 2015, 70, A106. [CrossRe
38 of