SOLUTIONS FOR STABILIZING HYDROGEN PEROXIDE CONTAINING SOLUTIONS
This invention relates to stabilising solutions for stabilising hydrogen peroxide, to stabilised hydrogen peroxide-containing biocidal compositions and to methods for using same. More specifically the invention provides a concentrate which is active as a stabilizer for hydrogen peroxide and to disinfectant solutions formed by mixing the concentrate and hydrogen peroxide.
Oxidizing agents are employed in large quantities in industry for disinfectant and sanitizing application. Thus chlorine and hypochlorite compounds are traditionally used for water treatment, such as potable water supplies and swimming pools, as well as for environmental cleansing operations and the treatment of food-producing and other equipment where hygienic conditions are paramount. Thus known procedures for maintaining desired bactericidal levels in water supplies, swimming pools and circulating baths of the "Jacuzzi" type generally rely upon the use of sources of chlorine or hypochlorite ions in order to eliminate viable pathogenic organisms. Other known procedures include exposing the water to ozone and circulating the water through irradiating zones where the water is exposed to high levels of UV radiation.
The use of chlorine and hypochlorite for treating water supplies has the disadvantage that chlorine escapes to the environment where it can have a pronounced polluting effect and organic compounds present in the water become chlorinated to produce toxic organo-chlorine compounds. The use of ozone and U.V. irradiation involves the use of expensive equipment and high running costs.
Hydrogen peroxide is well known as an oxidizing agent and biocide and has found widespread application in limited fields such as, for example, the carbon in pulp process, in metallurgical recovery and to provide nascent oxygen.
Hydrogen peroxide has many advantages over chlorinating materials in disinfectant and sanitizing applications. For example, hydrogen peroxide is not a pollutant, decomposing to oxygen and water. It also does not react with ammonia, thus avoiding potential undesirable by-products and its use can be controlled to provide selective oxidation. Hydrogen peroxide does react efficiently with sulphur compounds in aqueous media removing noxious odours. Thus it oxidizes hydrogen sulphide to produce water and elemental sulphur. An indication of the efficiency of the product in this regard is the fact that H_S present at a concentration of 1 ppm in water can be completely oxidized by about one quarter of the quantity required using suitable chlorination products. Hydrogen peroxide is also effective against a broad range of bacteria including some which have become resistant even to chlorine, such as Pseudomonas aeruginosa.
However hydrogen peroxide is unstable with respect to its decomposition into water and oxygen, this process being accelerated in the presence of catalysts which are numerous and varied. Examples of these catalysts include metal surfaces, metal oxides and even some soluble salts, for example those of iron and copper. Thus the decomposition process is accelerated in the presence of a range of metal ions, mainly iron, copper, vanadium, nickel, chromium and manganese. These metals can decompose hydrogen peroxide by catalytically controlled chain reactions. Some of the metals form stable complexes with the hydrogen peroxide.
Decomposition of hydrogen peroxide also occurs in the presence of organic material.
Mechanisms for hydrogen peroxide decomposition include hydrogen ion abstraction, radical chain termination occurring by combination with solution ions or attack by radical scavengers such as aromatic amines. Homolytic and heterolytic bond cleavage also occurs.
The decomposition process is also affected by pH and the presence or otherwise of stabilizers.
Because of the tendency of hydrogen peroxide to decompose, non-stabilized hydrogen peroxide is of limited use for many disinfectant/antiseptic applications.
With this tendency to decompose, the shelf-life of hydrogen peroxide is short and even in situations where nascent oxygen is required, this is generally generated too quickly for efficient use thereof. In order to prolong the useful life of hydrogen peroxide, particularly in stock solutions thereof, so called "inhibitors", i.e. substances which inhibit the decomposition of hydrogen peroxide to oxygen and water, may be used. Known inhibitors include hippuric acid, acetanilide and also phosphoric acid. However all of these are associated with various disadvantages such as limited effectiveness, high cost, non-degradability and odour.
A further use of hydrogen peroxide (as an aqueous solution) is as an antiseptic. This use, which relies upon the strong bactericidal properties of hydrogen peroxide, has also been limited because of the tendency of hydrogen peroxide to become deactivated by organic materials.
The patent literature discloses many examples of hydrogen peroxide stabilizers, most of which have little effect on hydrogen peroxide stability per se but appear to act rather as inhibitors of decomposition catalysts of the kind described above. Thus various complexing organic compounds have been suggested as sequestering or chelating agents.
In EP 0209228 it has been proposed to form stabilized solutions of hydrogen peroxide by the addition of aminophosphonate chelating and aromatic amine free radical scavenging agents. This patent also proposes, inter alia, the use of a surfactant for control of the physical qualities of the stabilized hydrogen peroxide solution.
It is also known from the literature that non-stabilized 35% hydrogen peroxide is most stable in the pH range 2.5 to 4.5- At pH 3 the decomposition rate per day at 100°C is extremely low but rises to 90% at pH 1. In GB-A-2189 394 the use is described of an inorganic acid, such as phosphoric acid, together with an organic acid, such as citric or tartaric acid as sequestering and buffering agents to provide a stabilizer concentrate, a source of silver ions also being provided as a synergist, to give a stabilized hydrogen peroxide solution with activity as a disinfectant in the food industry and for water treatment.
Specifically GB-A-2189 34 describes a concentrate which can be mixed with hydrogen peroxide for a disinfectant. According to GB-A-2 189 394, this concentrate is made by mixing a solution of an aqueous inorganic acid having a pH less than or equal to 1.6 in deionised water, at between 50 and 60"C with colloidal silver, a silver salt or silver salt complex. Tartaric and/or citric acids are stated to be suitable stabilisers for use in combination with the silver compounds. The specification states that the new agents described are suitable for numerous applications, including use in water disinfection for swimming pools and hot whirlpools. However this proposed use ignores the high expense of silver and also the fact that in the aforementioned uses, it is highly undesirable for silver containing compounds to be allowed to contact the polymer-based decorative surfaces (including plastics fittings, coloured rubber connectors and accessories and painted surfaces) which are inevitably present in swimming pools and other bathing facilities such as, for example,
Jacuzzis. Accordingly, the compositions of GB-A-2 189 394 have failed to achieve acceptance for these uses.
The compositions of GB-A-2 I89 394 further have been found to be less than satisfactory in fulfilling their prime objective of providing a satisfactory degree of longevity for hydrogen peroxide stock solutions. On investigation the reason for this appears to be the lack of appreciation that tartaric acid has an unexpectedly high stabilizing ability when used at relatively high concentrations in combination with citric acid. More specifically it has now been found that citric acid and tartaric acid, when present together in specific proportions wherein a relatively high concentration of tartaric acid is maintained have an enhanced and apparently synergistic stabilizing potential.
An object of the present invention is to avoid the aforementioned disadvantages and to provide a concentrate comprising phosphoric, citric and tartaric acids in specific proportions so that the concentrate has the property of stabilizing hydrogen peroxide solutions to provide a disinfectant which possesses sustained high activity even at extremely low concentrations.
According to one aspect of the invention there are provided aqueous stabilizing solutions for stabilizing hydrogen peroxide, comprising the following constituents
Citric acid 1 to 7 mass percent/vol. Tartaric acid 7 to 12 mass percent/vol.
and a chelating and/or buffering agent. Preferably the chelating and/or buffering agent is present in a sufficient concentration to effect substantially complete chelation of metal ions capable of catalyzing the decomposition of hydrogen peroxide.
Further according to the invention the chelating and/or buffering agent is preferably phosphoric acid and the citric, tartaric and phosphoric acids are provided in the ratio 1:4:2, the concentrations thereof being selected to provide a concentrate which has a pH between 1.5 and 3 and a maximum dissolved solids content of 38000 pp . As stated above non- stabilized hydrogen peroxide is most stable in the range 2.5 to 4.5 and a pH of the stabilizing solution in the stated range is effective suitably to buffer and enhance the stability of the stabilized product.
It has been found that a stabilizer concentrate solution incorporating the aforesaid constituents within the specified concentration ranges provides protection of a high order against decomposition of hydrogen peroxide and that disinfectant solutions formed therewith possess superior activity against pathogenic micro-organisms found, for example, in brewery installations.
In these embodiments, the stabilising solution may include silver ions in the concentration range 5 to 30 parts mass % by volume. The silver ions may be provided by means of a soluble silver salt, the silver providing for enhanced biocidal activity in the stabilized hydrogen peroxide solution, rendering the final solution efficacious in effluent treatment. The silver ions are preferably provided by a soluble silver salt such as at least one of silver nitrate, silver sulphate and silver nitrite, or by use of silver chloride. Where silver nitrate is used, the preferred ratio of the constituents silver nitrate to citric acid to tartaric acid to phosphoric acid is approximately 13:1:4:2.
The concentrate may be made simply by dissolving silver nitrate in de-ionised water and raising the temperature of the solution to approximately 30°C before adding the required amounts of citric and tartaric acid. This is followed by the phosphoric acid which is stirred into the solution for
approximately one hour followed by an ultra-violet ray blocker if required, and the resulting solution may then be filtered through a 45μm millipore filter before use.
It will be appreciated that the stabilizing agents in the concentrate protect hydrogen peroxide against rapid decomposition, particularly in the presence of silver ions and that the silver ions act in synergy with the hydrogen peroxide to enhance the bactericidal properties of the disinfectant.
According to a further aspect of the invention, stabilizing compositions for stabilizing hydrogen peroxide have been devised which enable effective hydrogen peroxide-based biocidal compositions to be produced which do not rely upon the presence of silver.
According to this aspect of invention there are provided aqueous stabilizing solutions for stabilizing hydrogen peroxide, comprising the following constituents
Citric acid 1 to 7 weight percent Tartaric acid 7 to 12 weight percent
and a chelating and/or buffering agent. Preferably the chelating and/or buffering agent is present in a sufficient concentration to effect substantially complete chelation of metal ions capable of catalyzing the decomposition of hydrogen peroxide, said compositions being further characterized by the substantial absence of silver.
Preferably in accordance with each aspect of the present invention, the chelating and/or buffering agent comprises phosphate ions which may be provided by incorporating phosphoric acid into the composition. The phosphoric acid is preferably provided in a concentration of from 2 to 6 weight percent. As above, the pH is preferably from 1.5~3-
According to yet another aspect of the invention the concentrates provided according to each aspect of the invention incorporate an ultra-violet ray blocker, preferably acetanilide, to provide increased stability especially to highly diluted disinfectant solutions in high ultra-violet ray exposure conditions. Such ultra-violet blocker is added to the concentrate in the proportion of 0.02 to 0.1#.
A particularly preferred stabilizing composition according to the invention includes the aforementioned constitutents in the following approximate preferred ratio:
Citric acid:tartaric acid:phosphoric acid = 1:4:2
Especially preferred stabilizing solutions have a maximum total dissolved solids content of 38OOO ppm.
The invention further provides hydrogen peroxide-containing compositions stabilized by addition of the stabilizing compositions defined above. Such stabilized hydrogen peroxide solutions may be prepared by mixing aqueous hydrogen peroxide with the aforementioned stabilizing solutions in the following concentration ratios:
Hydrogen peroxide 99.7 to 97 mass percent/vol. Stabilizing solution 0.25 to 3O mass percent/vol.
Preferably the concentrate is added to hydrogen peroxide by simple mixing in the range 1 to 99 to 1 to 199 of stabilizer concentrate to hydrogen peroxide. Such stabilized hydrogen peroxide disinfectant solutions have an extended shelf life and may be used for treatment of drinking water at 1 to 34 ppm; in swimming pools at 0 to 100 ppm and for surface disinfection of equipment and the like at a concentration of 0.1 to 0.5 .
Expressed in terms of mass percent/vol of the specified constituents the hydrogen peroxide-containing compositions according to the invention preferably comprise citric acid and tartaric acid in the following concentration ranges expressed as mass percent/vol aqueous H-O-:
Citric acid 0.0025 - 0.21 weight percent Tartaric acid 0.0175 - 0.36 weight percent.
Said hydrogen peroxide-containing composition according to one aspect of the invention are further characterized by the substantial absence of silver.
Also according to the invention a quaternary ammonium salt such as tetra-n-propyl ammonium hydrogen sulphate or other lipid soluble quaternary ammonium salt such as that sold under the trade name of BELLACIDE 350, is incorporated into the disinfectant solution. It is believed that such salt assists the transport of ions through the cell wall of bacteria thereby enhancing the biocidal activity of the product.
The said quaternary ammonium salt may be incorporated directly into the final made up hydrogen peroxide solution in concentration of 5 to 20% .
The quaternary ammonium salt, however, causes a reaction in the presence of silver ions giving rise to a precipitate and making it unsuitable for use in cases where silver has been added to the concentrate.
It has been found that when silver-containing stabilizing solutions are produced by the procedures described in GB-A-2 189 394 problems arise due to the formation of a yellow precipitate (believed to be silver phosphate) and as indicated above the biocidal potential of the resulting solutions is limited.
There is further provided in accordance with the present invention, a novel process for producing the silver-containing aqueous stabilizing solutions according to the invention which avoids disadvantages of known procedures, particularly those described in GB-A-2189 394.
According to this aspect of the present invention there is provided a method of producing a silver-containing stabilizing solution for stabilizing hydrogen peroxide which comprises the following steps carried out in the order specified:
A. forming an aqueous solution comprising a water soluble silver salt at a temperature of from 20 to 4θ°C
B. forming an aqueous solution comprising a water soluble silver salt, tartaric acid and citric acid from the solution formed in Step A
C. forming an aqueous solution comprising a water soluble silver salt, tartaric acid, citric acid, and phosphoric acid from the solution formed in Step B
In carrying out Step B solid citric acid and tartaric acid may be dissolved in the solution formed in Step A. Alternatively, the citric acid and tartaric acids may be dissolved in water and the resulting solution mixed with the solution formed in Step A.
Step C may be caried out simply by mixing the solution from Step B with aqueous phosphoric acid.
The preferred ingredients and proportions thereof are as specified above with respect to the aqueous stabilizing solutions per se.
As used herein the term "phosphoric acid" designates any of ortho-, metaand pyro- phosphoric acids and mixtures thereof. Preferably orthophosphoric acid is used.
The invention further provides the use of a hydrogen peroxide-containing composition as defined herein as a disinfectant for water, especially for a swimming pool, or Jacuzzi. Such use involves periodically adding a biocidally effective amount of a a hydrogen peroxide-containing composition as defined herein.
The following examples illustrate the invention:
EXAMPLE 1
A stabilizing solution is provided for the stabilization of 50 volume hydrogen peroxide.
The stabilizing solution has the following composition and characteristics:
PH 2-3 total dissolved solids 38000 specific gravity 1.06 citric acid 2.10 mass #/vol tartaric acid 8.00 mass #/vol phosphoric acid 4.30 mass #/vol
The concentrate was made up by dissolving 80 gm of tartaric acid and 21 gm of citric acid in 500 ml de-ionised water at room temperature using a standard laboratory PYREX beaker suitably cleaned with de-ionised water. To this solution there was added 0 gm 85% orthophosphoric acid and the volume was made up to 1000 ml with de-ionised water and stirred for one hour until the solution was homogeneous. After filtration through a 45um millipore filter the concentrate solution was added to 50 volume H_0_ in the ratio 1 part by volume of the stabilizer concentrate to 199 parts of the 0 volume hydrogen peroxide solution.
The concentrate was made up by dissolving 80 gm of tartaric acid and 21 gm of citric acid in 500 ml de-ionised water at room temperature using a standard laboratory PYREX beaker suitably cleaned with de-ionised water. To this solution there was added 0 gm 85% orthophosphoric acid and the volume was made up to 1000 ml with de-ionised water stirred for one hour until the solution was homogeneous.
After filtration through a 45μm millipore filter the concentrate solution was added to 0 volume H_0_ in the ratio 1 part by volume of the stabilizer concentrate to 199 parts of the 50 volume hydrogen peroxide solution.
Not only does the concentrate solution stabilize the hydrogen peroxide against decomposition into water and oxygen, but the stabilizing solution itself is biodegradable and, furthermore, does not have any adverse characteristics of the type associated with the use of other stabilizers such as hippuric acid and peracetic acid.
It is envisaged that the stabilized hydrogen peroxide solution will find extensive use in various disinfectant applications, the reduction of algae growth, the reduction of aldehydes, phenols, cyanides, sulphides and mercaptans, photo-effluent treatment, the reduction of sulphur and nitrogen oxides, odour removal and chlorine replacements.
The disinfectant product of this example is particularly useful for disinfectant of swimming pools and does not have the disadvantages mentioned above with respect to the use of hypochlorites. It was tested in terms of "Standard Method 682" of The South African Bureau of Standards to measure its efficacy as an algaecide and bactericide for swimming pool use. The standard requires that no growth of algae should occur within 28 days after innoculation of test samples of the disinfectant solution with algae growth medium and that no growth of bacteria should occur within the first 48 hours after innoculation. Bactericidal activity was tested using 0.1 peptone water as cultivation medium, incubating the bottles at 37°C and using as test organisms a mixture of Escherichia coli SATCC Esc 25; Staphylococcus aureus SATCC Sta 53; and Pseudomonas aureuginos SATCC Pse 2 containing approximately 10000 bacteria per ml.
The results of the test using untreated control and the disinfectant solution of Example 1 at concentrations of 10, 20 and 3 mg/litre are set out in Table I
TABLE I
It will be seen that the disinfectant of the invention provided eeffective control of micro-organisms in the standard test using 36mg/litre of the disinfectant solution, i.e. 36 ppm in swimming pool applictions. Since use of the disinfectant at 60-80 ppm in swimming pool applictions is permitted, the disinfectant solution of Example 1 is shown to be a highly effective swimming pool disinfectant product.
EXAMPLE 2
In the second example of the invention a stabilizing solution for use in stabilizing a 35 volume hydrogen peroxide solution to give a highly effective bactericide is provided.
This stabilizing solution has the following typical composition and characteristics:
PH 0.96 total dissolved solids 195000 specific gravity 1.27 silver nitrate 26.64% mass/volume
15 citric acid 2.10 mass/volume tartaric acid 8.00% mass/volume phosphoric acid 4.30% mass/volume
The concentrate was made up by dissolving 266.4 gm silver nitrate in 500 ml de-ionised water. The solution was heated to 30°C while stirring and 21 gm citric acid and 80 gm tartaric acid were then added and allowed to dissolve before adding 50 gms of 85% orthophosphoric acid. The solution was made up to 1000ml using de-ionised water and stirred for 2 hours. The- solution was then filtered through a 4 μm millipore filter.
After filtration, the stabilizing solution was added to the 35 volume hydrogen peroxide in the ratio of 1 part by volume of the stabilizing solution to 199 parts by mass of the 35 volume hydrogen peroxide solution to provide a disinfectant having from to 10 ppm of the stabilizing agent and about 1000 ppm of silver ions.
The concentrate stabilizes the hydrogen peroxide against decomposition, particularly in the presence of the silver ions and the silver ions provide enhancement of the hydrogen peroxide insofar as its bactericidal properties are concerned. The disinfectant is effective at 0.01 to 0.5% dilution for sanitization of food machinery and surface disinfection in general.
In order to rate the silver-containing disinfectant solution of Example 2 it was compared with three commercially available
hydrogen peroxide/peracetic acid disinfectant compositions at their recommended use dilutions of:-
Example 2 disinfectant 0.5%
Commercial Disinfectant A 0.4%
Commercial Disinfectant B 0.15%
Commercial Disinfectant C 0.2%
These products were tested against cultures of Bacillus, E. Cloacae. Pepiococcus spp., Lactobacillus spp., Sarcina which were grown in ULM overnight and cultures of 2036 (Yeast) , Picia, Candida and S. Ellipsoideus which were grown up in MYGP broth overnight. The grown cultures were then bulked and spun down at 25 000 rpm for 10 minutes. The supernatant was discarded and the pellet re-suspended in 100 ml of saline to make a suspension of approximately 10 cells/ml.
The disinfectants were made up to their required concentrations and the amount of caustic required to neutralize 5 nil of each of them was determined. The specific amount of caustic were then measured into bottles and sterilized.
1 ml of the prepared culture was innoculated into 50 ml of each of the disinfectant solutions and after intervals of 5. 10, 15, 20, 25 and 30 minutes ml was removed and immediately neutralized by caustic. 0.2 ml of the neutralized solution was plated onto each of the LMDA and WLN and incubated at 30°C and 25°C respectively whereafter bacterial counts were made.
The results are set out in Table II
TABLE II
M I N U T E S
0) I Disinfectant m B (0,15%)LMDA 5 Bacillus Bacillus 6 Bacillus 5 Bacillus 5 Bacillus 5
Bacillus
WLN 0 0 0 0 0 0
Disinfectant C (0,2%) LMDA 300* 300* 200* 200* 100* 100*
WLN TNTC* TNTC* TNTC* TNTC* TNTC*
* = mixed culture
TNTC = too numerous to count
These results show that with a culture containing approximately 10 cells/ml, the disinfectant of Example 2 was the most effective with disinfectants A & B being effective as well. However, disinfectant C did not compare satisfactorily with the other compositions tested.
In order to compare the disinfectant product of Example 2 with a commercial iodophor, brewery fermentation vessels were sterilized using the normal commercial idophors and the Example 2 product of the invention. Repeated disinfection runs were made using the iodophor and the product of Example 2 separately and the sanitizing effect of the two products was determined by taking swabs from the test vessels and subjecting them to quantitative microbiological analysis. These analyses indicate whether or not the vessel is sterile. A vessel which is sterile is said to be "under control".
The results are set out in Table III from which it will be seen that the disinfectant of the invention provided substantially improved sanitation control of brewery equipment.
The product was further compared with a commercial stabilized hypochlorite disinfectant for sanitization of a brewery pasteurizer unit. Repeated disinfection runs were made on the unit after each operation thereof by depositing the test disinfectant in the sump of the unit. In the case of the hypochlorite sufficient product was used to maintain a free chlorine residual < 0.5 PPπ while the disinfectant of Example 2 was used to maintain a residual of hydrogen peroxide Of 20 - 50 ppm.
The products were in each case fed continuously to the machine sumps to maintain the required residuals. As an operation standard acceptable bacterial counts were taken to be < 10 micro-organisms/ml and wild yeasts count at < 10 organisms/ml. Each test was run over a period of 24 hours.
The results are set out in Tables IV and V from which it will be seen that the stabilized hydrogen peroxide disinfectant solution of the invention was superior.
* = feed to sump 1 interrupted for 12 hours TNTC = too numerous to count
Example 3
Stabilized hydrogen peroxide disinfectant solution containing a quaternary ammonium salt.
The disinfectant solution produced in terms of Example 1 was used and 5 mass % by volume of BELLACIDE 350 was added thereto.
The resulting disinfectant solution is particularly suitable for use in the disinfectant of brewery equipment. In order to compare the disinfectant solutions of Examples 1 to 3 tests were run on brewery pasteurizers for slime control using the three products.
In each case the products were fed into the sumps of brewery pasteurizers to maintain machine residual of 20 to 50 ppm of hydrogen peroxide and the disinfectant was distributed through the machines using the normal circulating pumps.
The pasteurizers were run for a period of 4 days and visual inspections were made at 24-hour intervals. The pasteurizer using the disinfectant product of Example 1 developed fairly heavy slime after 48 hours indicating the growth of micro-organisms is excess of 10 organisms/ml. The pasteurizing equipment using the silver-containing disinfectant solution of Example 2 provided an operationally clean machine indicating that the disinfectant was effective to control micro-organisms to provide a count of less than 10 organisms/ml.
The pasteurizing equipment using the product of Example 3 was even cleaner than that using the disinfectant of Example 2 on visual inspection after 4 days.
Thus the disinfectant product of Example 3 is at least as effective as that of Example 2 containing silver ions.
Example
Dilute stabilized hydrogen peroxide solution with ultra-violet blocker.
In order to test the efficacy of acetanilide to prevent degradation of the .hydrogen peroxide solution, samples were prepared according to Example 1 at 0.05% and acetanilide was added to some of the samples which were then irradiated using a 4θw ultra-violet light source suspended in a cabinet about 20 cm. above the samples.
The irradiation was continuous over a period of 24 hours and two different sources of commercial 50% volume hydrogen peroxide were utilized.
The results of the test are set out in Table VI.
TABLE VT
ULTRA-VIOLET STABILITY OF DILUTE H20 S0LUTI0Ns
Set 1
Set 2
SUBSTITUTE SHEET
Table VI illustrates the effectiveness of acetanilide but also shows that the source of hydrogen peroxide plays an important role.
Initial tests have further indicated that not only do the stabilizing solutions stabilize the hydrogen peroxide against rapid decomposition into water and oxygen, but the stabilizing solution themselves, especially the silver-free embodiments, are biodegradable and, furthermore, do not have any adverse characteristics of the type associated with the use of other stabilizers or inhibitors such as hippuric acid, acetanilide, orthophosphoric acid and peracetic acid.
It is envisaged that the stabilized hydrogen peroxide solution will find extensive use in various disinfectant applications, the reduction of algae growth, the reduction of aldehydes, phenols, cyanides, sulphides and mercaptans, photo-effluent treatment, the reduction of sulphur and nitrogen oxides, odour removal and chlorine replacements.
The resultant solution desirably contains approximately 700 ppm of the stabilizing agent and (if used) about 1000 ppm of silver ions.
It will readily be appreciated that the stabilizing agent stabilizes the hydrogen peroxide against decomposition. In the embodiments characterised by the presence of silver ions, the silver ions constitute an enhancement of the hydrogen peroxide solution insofar as its bactericidal properties are concerned.
It is particularly envisaged that the resultant solutions according to the invention (especially the silver-free embodiments) will be used as a disinfectants and biocides even to the extent of disinfecting potable water and other water sources such as swimming pools for example.
Stabilized hydrogen peroxide solutions produced in accordance with Example 1 and Example 2 were used as biocidal agents in swimming pools at various concentrations and the results are shown in the following Table.
TABLE VII
RESULTS
*53-28% mass volume silver nitrate
It can be seen from the above Table that the composition of Example 1 was effective in eliminating bacterial growth after 48 hours at each of the three concentrations used whereas for the silver-containing compositions of Example 2, bacterial growth was inhibited only at the highest concentration. However at this concentration, the level of silver was excessively high to enable the composition to be used as a swimming pool disinfectant, in view of its deleterious effects on rubber and plastic swimming pool fittings. That the composition of Example 1 had a complete inhibitory effect at each of the concentrations tested and furthermore inhibited algae growth for a substantial period of time was particularly surprising as such properties of a disinfectant composition containing hydrogen peroxide as the sole disinfecting agent and
in the substantial absence of silver had not been suspected hitherto.
EXAMPLE 5
Stabilized hydrogen peroxide solutions were prepared as follows:
A - according to Example 1
B - according to Example 2
C - according to Example 1 of GB-A-2 189 394
D - commercially availabe product (ADDOX)
The resulting solutions were assessed for their disinfectant ability by testing their biocidal activity against four test organisms. The results are given in the following Tables VIII, IX, X and XI.
The superiority of the compositions of the invention is apparent.
TABLE A ACCORDING TO EXAMPLE 1
(DESTRUCTION RATES IN PERCENT)
15 MINUTES 30 MINUTES 60 MINUTES
20 C 4o°c 20 C 40°C 20 C 4o°c
30ppm
E. coli ft 0?) S. aureus P. aeruginosa C. albicans
75ppm E. coli S . aureus P. aeruginosa C . albicans
TABLE B ACCORDING TO EXAMPLE 2
(DESTRUCTION RATES IN PERCENT)
15 MINUTES 30 MINUTES 60 MINUTES
20°C 4θ°C 20°C 40°C 20°C 4o°c
30ppm
E. coli S. aureus P. aeruginosa C. albicans
75ppm E. coli S. aureus P. aeruginosa
C. albicans
TABLE C ACCORDING TO EXAMPLE 1 OF GB-A-2 1893
(DESTRUCTION RATES IN PERCENT)
15 MINUTES 30 MINUTES 60 MINUTES 90 MINUTES 120 MINUTES
lOppm
E. coli 40.0 31.8
00
K. pneumoniae 28.9 35.0 35.3
20ppm
E. coli 17.6 30.0 40.9
K. pneumoniae 4.6 39.1 15.9 38.0 45.0
30ppm
E. coli 13.3 29.4 35.0 54.5
K . pneumoniae 20.7 33.0 14.8 40.0 55.6
TABLE D COMMERCIALLY AVAILABE PRODUCT (ADDOX)
TEST CONCENTRATION %
Value
Count 0.0075 0.005 0.002 (Sterile
TEST GERM per ml 10 0.1 0.05 0.01 (75 ppm) (50 ppm) (20 ppm) 0.001 0.0005 Water)
CO E.Coli 53χlθ6 (+) c K.Pneumoniae 6.1xl0 ++
S.aureus 50x10 ++
H
C S.faecalis 36xl06 H (+) rπ P.mirabils 24xl06 ++ x S.sporogeres 2.1x10 ++ ++ m m H
Explanation of symbols
= No growth
(+) = Slight growth
+ = Evident growth
++ = Strong growth
For each preparation a growth control test was carried out under the same experimental conditions but without the addition of A D D 0 X. All the germs tested showed strong growth in the control test.