[0001] The present invention relates to the field of beverage dispense line cleaning. More
particularly, but not exclusively, it relates to a method for removal of biofilm and
other microscopic contaminants from beer lines.
[0002] In licensed premises, each dispensing tap is usually served by a system of tubing
and valves, leading from a keg or other storage vessel kept in a cellar, or equivalent,
to the dispensing tap on a bar counter. Such lines are used for many products, both
alcoholic and non-alcoholic, but they may be known by the general name of "beer lines".
[0003] It is a perennial problem to keep the beer lines clear of contamination, both for
health reasons and to avoid tainting the taste of the beverage. This may take the
form of bacterial contamination and/or yeast growth, which can normally be kept at
bay with regular use of beer line cleaners, such as those based on mixtures of alkali
metal hydroxides and hypochlorites. These both clean and disinfect the beer lines.
However, such beer line cleaners are less effective against biofilm.
[0004] Biofilm is a generic term for a layer of contamination which can build up on the
interior wall of a beer line. The exact composition can vary, but biofilm generally
comprises a matrix of long-chain polysaccharide molecules, which adhere strongly to
the wall of the beer line, and can entrap or bond to other contaminants. Bacteria
and other biological cells can easily be incorporated into biofilm, anchoring them
firmly and, to a great extent, protecting them from the action of conventional beer
line cleaners.
[0005] Biofilm is very tenacious and resistant to conventional cleaners and may require
steeping in conventional beer line cleaner for many hours to penetrate and break down
the film. Any unremoved biofilm not only acts as a source of re-infection of the line,
but may also subsequently come free and enter the beverage being dispensed. The particulate
thus produced can lead to an unsightly haze in beer or other beverage pulled through
the beer line, and can even be large enough to be seen by the naked eye (so-called
"floaters").
[0006] There may also be "off flavours" present in the beer line due to phenol, chlorophenol,
hydrogen sulphide, diacetyl or DMS given off by the biofilm, and these should be removed
before they taint the next passages of beer or other beverage.
[0007] There is hence a need for a rapid, effective and safe method for removing biofilm
from beer lines.
[0008] It is therefore an object of the present invention to provide a method for cleaning
the interior of beer lines which can rapidly and thoroughly break down and remove
biofilm from the beer lines.
[0009] According to the present invention, there is provided a method of cleaning a beverage
dispensing system comprising the steps of introducing into the system an alkaline
treatment solution, clearing the system and then introducing a second treatment solution
containing chlorine dioxide.
[0010] Preferably, the chlorine dioxide treatment solution is generated in situ by mixing
an acid with a first precursor solution comprising chlorite ions, such as sodium chlorite.
[0011] Advantageously, the acid may be a solid, such as isocyanuric acid or a salt thereof.
[0012] Alternatively, the acid may be an organic carboxylic acid or a salt thereof.
[0013] The acid may be a di- or tri-carboxylic acid.
[0014] The organic carboxylic acid may be citric acid, preferably as an aqueous solution.
[0015] A solid acid, such as isocyanuric acid, may be provided in tablet form, advantageously
corresponding to a predetermined dose thereof.
[0016] Such a tablet may be adapted for admixture with a predetermined quantity of chlorite
solution to generate a desired amount of chlorine dioxide.
[0017] The chlorine dioxide is preferably provided as an aqueous treatment solution comprising
between 50 and 1000 ppm of available chlorine dioxide.
[0018] Advantageously, the solution of chlorine dioxide comprises between 100 ppm and 500
ppm of available chlorine dioxide.
[0019] Optionally, said solution may comprise between 200 ppm and 500 ppm of available chlorine
dioxide.
[0020] The concentration is advantageously in the region of 250 ppm.
[0021] The chlorine dioxide solution may be prepared by mixing pre-measured quantities of
a first precursor solution comprising chlorite ions and a second precursor solution
comprising an acid.
[0022] Said precursor solutions may each be provided in a respective container as a pre-measured
quantity of a solution of a reagent at a predetermined concentration.
[0023] A pair of two such containers may be conjoined as a double sachet, with a first sachet
containing the solution comprising chlorite ions and a second sachet containing the
acid solution.
[0024] After a predetermined time interval, an initially produced chlorine dioxide solution
may be diluted with water to form a treatment solution having a predetermined chlorine
dioxide concentration.
[0025] Embodiments of the present invention will now be more particularly described by way
of example.
Example 1
[0026] The reagents necessary for the method were provided in a pair of conjoined sachets
containing in one sachet 25ml of a solution containing 3.36% by weight sodium chlorite
and other oxychlorine species (equivalent to approximately 2% by weight of available
chlorine dioxide) and in the other sachet 10ml of a solution containing 50% by weight
citric acid. Both sachets were opened and the contents were mixed in a convenient
vessel. After five minutes, the initially colourless mixture became yellow, believed
to be due to the formation of chlorine dioxide in solution. The mixture was made up
to 2 litres with water, giving a solution containing approximately 250 ppm of available
chlorine dioxide.
[0027] Beer lines were first cleaned with a conventional alkaline beer line cleaner, and
the lines were flushed with water. The 250 ppm chlorine dioxide solution was then
introduced into the beer lines at the cellar end, and was pulled through until it
began to arrive at a dispensing tap at a bar end thereof. The solution was left to
take effect for between ten and twenty minutes, when the system was flushed with water.
The solution removed from the system contained sufficient broken down and suspended
biofilm to render it substantially opaque.
Example 2
[0028] A 6g tablet of isocyanuric acid was added to a 0.5 litre aliquot of 1% sodium chlorite
solution held in a polythene reagent bottle. The isocyanuric acid was allowed to dissolve
and mix for 7 minutes, in order to activate the release of chlorine dioxide into the
solution. The initially colourless solution became a straw yellow colour, believed
to indicate the presence of molecular chlorine dioxide in solution. This solution
(then containing approximately 10,000 ppm free ClO
2) was diluted 40:1 by adding it to 20 litres of water, giving a solution containing
approximately 250 ppm ClO
2, to serve as a beer line cleaner. Such a solution has been found to remain potent
and effective for at least a week.
[0029] Beer lines were first cleaned with a conventional alkaline beer line cleaner, and
the lines were flushed with water. The 250 ppm ClO
2 solution was then introduced into the beer lines at the cellar end, and was pulled
through until it began to arrive at a dispensing tap at a bar end thereof. The solution
was readily detectable by its colour and by its characteristic odour. This required
approximately half of the volume of solution prepared. The solution was left to take
effect for approximately ten minutes, and was then removed by being pulled off at
the dispensing tap, the remainder of the solution being simultaneously drawn into
the beer lines at the cellar end. This was left for a further ten minutes, and the
system was then flushed clear with water. The solution initially removed from the
system contained sufficient broken down and suspended biofilm to render it substantially
opaque.
[0030] The contamination level within a dispense system may be measured by bioluminescence
methods, assaying for ATP resulting from bacteria, yeasts and the like. Tap water
typically has a level of 60-70 RLU (relative light units). A badly contaminated beer
line as described above had an initial contamination level of 6500 RLU, but after
only ten minutes treatment with the chlorine dioxide solution, this fell to 303 RLU.
In previous tests, using conventional alkaline beer line cleaners, such a reduction
in contamination typically required treatment for at least one or two hours.
[0031] It is envisaged that treatment of a system with a chlorine dioxide solution should
follow a treatment with a conventional alkaline beer line cleaner. For example, if
the contamination in the system is resistant to removal with the conventional alkaline
beer line cleaner, the system may be flushed with water then treated with a chlorine
dioxide solution to clean and disinfect the system more rapidly.
[0032] Chlorine dioxide solution used on its own acts only as a surface treatment. In order
for it to attack and destroy the biofilm, it is therefore necessary in practice for
such a treatment to be used following an initial treatment with conventional alkaline
cleaner which exposes the biofilm to the chlorine dioxide.
[0033] It is found that a chlorine dioxide solution as described above may be stored for
up to a week without significant loss of effectiveness. However, it may be preferable
on health and safety grounds to make up the solution only as and when required.
[0034] While many oxychlorine species are known to have oxidising properties and may thus
have some disinfectant properties, chlorine dioxide has been found to be particularly
effective at attacking and breaking up biofilm such as is formed on the interior walls
of beer lines. It is also lethal to any bacteria, yeasts, mould, fungi and other cellular
organisms liberated by the break up of the biofilm. No adverse effects on beer lines
have been noted, as chlorine dioxide does not appear to react with the materials of
construction normally employed.
[0035] The preferred reagents for generating chlorine dioxide are sodium chlorite (also
known as sodium chlorate (III)) and citric acid, which react together to give chlorous
acid, HCℓO
2. Chlorous acid may equally conveniently be generated from sodium chlorite and isocyanuric
acid, H
3C
3O
3N
3. Isocyanuric acid is conveniently available in solid form, such as in tablet form,
which renders accurate dosage measurement easy.
[0036] Chlorous acid is not stable in acid solution and slowly decomposes to give chlorine
dioxide, as follows:-

[0037] A solution containing 3.36% by weight sodium chlorite may contain potentially up
to 2% by weight ClO
2, but practically produces only approximately 1% by weight of available chlorine dioxide.
[0038] The method described above provides a fast, effective and safe means to remove biofilm
from a beverage dispensing system. It is particularly convenient to use and represents
at least an order of magnitude improvement in effectiveness and rapidity over existing
methods and cleaning agents.
1. A method of cleaning a beverage dispensing system comprising the steps of introducing
into the system an alkaline treatment solution, clearing the system and then introducing
a second treatment solution containing chlorine dioxide.
2. A method as claimed in claim 1, wherein the chlorine dioxide treatment solution is
generated in situ by mixing an acid with a first precursor solution comprising chlorite
ions, such as sodium chlorite.
3. A method as claimed in claim 2, wherein the acid is a solid, such as isocyanuric acid
or a salt thereof.
4. A method as claimed in claim 2, wherein the acid is an organic carboxylic acid or
a salt thereof.
5. A method as claimed in claim 4, wherein the organic carboxylic acid is citric acid,
preferably as an aqueous solution.
6. A method as claimed in any one of the preceding claims, wherein the chlorine dioxide
is provided as an aqueous treatment solution comprising between 50 and 1000 ppm of
available chlorine dioxide, advantageously in the region of 250 ppm.
7. A method as claimed in any one of the preceding claims, wherein the chlorine dioxide
solution is prepared by mixing pre-measured quantities of a first precursor solution
comprising chlorite ions and a second precursor solution comprising an acid.
8. A method as claimed in claim 7, wherein said precursor solutions are each provided
in a respective container as a pre-measured quantity of a solution of a reagent at
a predetermined concentration, and wherein a pair of two such containers is conjoined
as a double sachet, with a first sachet containing the solution comprising chlorite
ions and a second sachet containing the acid solution.
9. A method as claimed in any one of claims 2 to 8, wherein, after a predetermined time
interval, an initially produced chlorine dioxide solution is diluted with water to
form a treatment solution having a predetermined chlorine dioxide concentration.