GB2118925A - Biocide - Google Patents
Biocide Download PDFInfo
- Publication number
- GB2118925A GB2118925A GB08310532A GB8310532A GB2118925A GB 2118925 A GB2118925 A GB 2118925A GB 08310532 A GB08310532 A GB 08310532A GB 8310532 A GB8310532 A GB 8310532A GB 2118925 A GB2118925 A GB 2118925A
- Authority
- GB
- United Kingdom
- Prior art keywords
- isothiazolone
- glutaraldehyde
- ppm
- composition according
- comprises adding
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/008—Prevention of corrosion or formation of deposits on pulp-treating equipment
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/50—Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
This invention relates to the elimination of bacterial deposits in cooling water systems and in water systems used in paper making. This is achieved by using a combination of glutaraldehyde and isothiazolone.
Description
SPECIFICATION
Biocide
This invention relates to the treatment of cooling water systems and of water systems used in paper pulping.
In industrial cooling water systems, for instance in industrial cooling towers, the water used is not, of course, sterile with the result that bacteria accumulate in the system and this quite commonly gives rise to a slimy deposit on the surfaces of the system which come into direct contact with the cooling water. A similar situation applies in paper making; slime can deposit on any of the surfaces with which the water comes into contact including the paper pulping bath on the paper web and in the recirculating back water pipework. A large variety of different treating agents have been used for the purposes of killing these bacteria and/or inhibiting slime formation. These chemicals include quaternary ammonium compounds, amines, isothiazolones, chlorine, phenols, including chlorinated phenols, chlorine-release agents, methylene-bis(thiocyanates), certain aldehydes and tin compounds.
It will, of course, be appreciated that the nature of the bacteria present in the system will vary and biocides which are suitable for use in some cooling water systems may well be inappropriate for use in other aqueous applications and vice versa.
As indicated above, one of the materials used in such systems are the isothiazolones. These are, however, relatively expensive materials. It has now surprisingly been found, according to the present invention, that glutaraldehyde in combination with isothiazolone produces a synergistic effect such that less of both materials is required in the combination to inhibit growth of the bacteria normally found in the water and also of the slime which can be deposited from such water than is the case when using each material separately. Accordingly, the present invention provides a method for the treatment of a cooling water system or of a water system used in paper making which comprises adding to the water, either directly or indirectly, glutaraldehyde and isothiazolone.
The isothiazolones used in the present invention are, in general, those having the formula:~
wherein R represents hydrogen or chlorine. A blend of these two isothiazolones is commercially available, the weight ratio of the chlorosubstituted compound to the unsubstituted compound being about 2.66:1.
Although it will normally be more convenient to add the two active ingredients as a mixture it is, of course possible to add them to the water separately.
In general, the weight ratio of isothiazolone to glutaraldehyde will vary from 1 :1 to 1:10, the preferred ratio being 1:3 to 1:5, especially about 1:4.
If the two ingredients are added as a mixture this will usually take the form of an aqueous solution. If desired, a stabilising agent to promote the stability of the isothiazolone on storage can be incorporated, such as cupric nitrate, for example as a 0.2% by weight solution. This is, in addition, to the magnesium chloride (typically 9%) and magnesium nitrate (typically 1 5%) which is often present in commercially available isothiazolones.
The product mixture will normally contain from about 1 to 15% by weight active ingredient, with the preferred concentration being 7.5 to 12.5% by weight, especially about 9.5%; this composition, with the preferred 1:4 weight ratio of components, can be made up from 12% by weight of isothiazolone (1 5% active content) and 15% by weight of glutaraldehyde (50% active content).
The precise concentration of use of the biocide will, of course, vary depending on the nature and amount of the bacteria present but, clearly, an amount effective to control the bacteria present should be used. With the preferred concentration in the product mixture one typically should use 25 to 500 ppm of product i.e. 25 to 500 mg of product, per litre of water, corresponding to roughly, 0.45 to 9 ppm of isothiazolone and 1.67 to 33.4 ppm of glutaraldehyde. In general at least 0.05 ppm up to, say, 1000 ppm, in particular 0.25 to 50 ppm, of isothiazolone and at least 0.2 ppm up to, say, 4000 ppm, in particular 1 to 200 ppm, of glutaraldehyde should be used.
In paper making the glutaraldehyde and isothiazolone may be added to the water directly, for example directly to the paper pulping bath or to the recirculating back water, or indirectly, for example to a holding tank containing, generally moist, pulp or along with one or more chemical additives used in paper making.Such additives include starch, for example potato or corn starch, titanium dioxide, a defoamer such as a fatty acid alcohol, a size, for example a rosin size based on abietic acid, a neutral size based on alkyl ketene dimer or a succinic acid anhydride based size, a wet strength resin such as, if neutral, an epichlorohydrin polyamide or, if acid, a melamine- or urea-formaldehyde resin, various polymers used as dispersants or retention aids such as polyacrylates, polymethacrylates, polyamides and polyacrylamides, clay, chalk, fillers such as carboxymethylcellulose, polyvinyl alcohol and optical brightening agents.
The following Examples illustrate the efficacy of the use of the combination of glutaraldehyde and isothiazolone as compared with the use of the individual ingredients alone. The samples listed below are real samples taken from commercial plants, the reference to "water" being to samples of water taken from the bulk of the system while the reference to "slime" refer to material containing microbiologically active material taken from surfaces in contact with the cooling water. The figures given show the concentrations needed to inhibit bacterial growth as determined by examination using agar plates at the indicated temperature.
Sample A-Water at 370C
(a) Concentration of Isothiazolone in mixture 0.94 ppm
Concentration of Glutaraldehyde in mixture 3.86 ppm
(b) Concentration of Isothiazolone alone 2.50 ppm
(c) Concentration of Glutaraldehyde alone > 20.00 ppm
Sample B-Slime at 370C
(a) Concentration of Isothiazolone in mixture 1.88 ppm
Concentration of Glutaraldehyde in mixture 7.52 ppm
(b) Concentration of Isothiazolone alone > 5.00 ppm
(c) Concentration of Glutaraldehyde alone 40.00 ppm
Sample G--Slime at 370C
(a) Concentration of Isothiazolone in mixture 60.47 ppm
Concentration of Glutaraldehyde in mixture 61.88 ppm
(b) Concentration of Isothiazolone alone 1.25 ppm
(c) Concentration of Glutaraldehyde alone > 40.00 ppm
Sample D-Slime at 20/22 C (a) Concentration of Isothiazolone in mixture 60.47 ppm
Concentration of Glutaraldehyde in mixture Q1.88 ppm
(b) Concentration of Isothiazolone alone 3.86 ppm
(c) Concentration of Glutaraldehyde alone > 40.00 ppm
Sample E-Slime at 370C
(a) Concentration of Isothiazolone in mixture 3.76 ppm
Concentration of Glutaraldehyde in mixture 15.04 ppm
(b) Concentration of Isothiazolone alone > 5.00 ppm
(c) Concentration of Glutaraldehyde alone > 40.00 ppm
Bearing in mind that glutaraldehyde is a much cheaper chemical than isothiazolone, it can be seen that the use of the combination as in the present invention is cheaper than the use of either ingredient alone for the same bactericidal and slimicidal action.
Further Examples illustrating the present invention are given below.
Examples comparing 1 :4 and 1 :11 ratio of isothiazolone to glutaraldehyde
Two biocide blends were prepared. Both of these contained the commercially available mixture of isothiazolones referred to in Examples reported earlier and glutaraldehyde. One of the these blends contained isothiazolones and glutaraldehyde in the ratio of 1:4 by weight (Blend A) and the other contained the same components in the ratio 1:11 by weight (Blend B). Both blends were prepared such as to contain the same total concentration of biocide.
Ratio of Total conc"
Isothiazolones Glutaraldehyde biocides of biocides
A 1.875% 7.5% 1:4 9.375%
B 0.775% 8.6% 1:11 9.375%
These two blends were then added at concentrations of 25 ppm, 50 ppm, 100 ppm and 200 ppm to three mixed-culture water samples at ambient temperature taken from industrial cooling systems.
Aliquots of these samples were removed after various times and incubated in nutrient agar at 220C for 3 days. The total counts were measured, and the percentage of bacteria killed calculated by reference to an untreated control.
Bacteria killed (%) in
Example Biocide Concfl(pprn) I hour 2 hours 4 hours 6 hours 24 hours
1 A 25 37% 60% 76% 99%
50 58% 83% 100% 100% - 100 79% 100% 100% 100%
200 100% 100% 100% 100% - 1 B 25 27% 42% 66% 83%
50 41% 74% 82% 98% - 100 66% 100% 100% 100%
200 100% 100% 100% 100% - 2 A 25 46% 63% 79% 94% - 50 65% 83% 99% 100% - 100 98% 100% 100% 100%
200 100% 100% 100% 100% - 2 B 25 33% 47% 68% 81% - 50 51% 66% 78% 96% - 100 79% 84% 93% 100%
200 96% 98% 100% 100% - 3 A 25 - 13% 17% 30% 86%
50 - 19% 53% 95% 91%
100 - 29% 97% 100% 94%
200 - 97% 100% 100% 97%
3 B 25 ~ 1 % 4% 28% 92%
50 - 2% 24% 92% 97%
100 - 2% 55% 97% 97%
200 - 10% 97% 99% 97%
It will be noted that the results obtained using Blend A (containing isothiazolones and glutaraldehyde in the ratio 1:4) are significantly better than those obtained using Blend B (containing isothiazolones and glutaraldehyde in the ratio 1:11).
Examples of the use of the biocide combination on samples from pulp and paper industry
The effect of the biocide combination was evaluated on two samples from the pulp and paper industry. Sample 1 was of a recirculating back water, and Sample 2 was a paper pulp slurry. The two biocides evaluated were biocide A, which contained 1.875% of the isothiazolone mixture, and 7.5% glutaraldehyde, and biocide B which contained 2.5% of the isothiazolone mixture. The samples were treated at ambient temperature with concentrations of 25 ppm, 50 ppm, 100 ppm, and 200 ppm of these two biocides. Aliquots of these samples were removed after various times and incubated in nutrient agar at 220C for 3 days. The total counts were measured, and the percentage of bacteria killed calculated by reference to an untreated control.
Bacteria killed { /0) in
Sample Biocide Concfl(ppm) 2 Hours 4 Hours 6 Hours 24 Hours
1 A 25 45% 58% - 95%
50 58% 67% - 97%
100 75% 100% - 97%
200 97% 100% - 100%
1 B 25 15% 47% - 95%
50 16% 55% - 96%
100 20% 98% - 99%
200 72% 100% - 100%
2 A 10 70% - 73% 93%
20 75% - 83% 97%
40 80% - 94% 100%
2 B 10 < 60% - < 60% < 60% 20 < 60% - < 60% < 60%
40 < 60% - 91% 94%
Claims (24)
1. A method for the treatment of a cooling water system or of a water system used in paper making which comprises adding to the water, either directly or indirectly, glutaraldehyde and isothiazolone.
2. A method according to claim 1 wherein the isothiazolone has the general formula:
wherein R represents hydrogen or chlorine.
3. A method according to claim 1 or 2 wherein the weight ratio of isothiazolone to glutaraldehyde isfrom 1:1 to 1:10.
4. A method according to claim 3 wherein the weight ratio of isothiazolone to glutaraldehyde is from 1:3 to 1:5.
5. A method according to claim 4 wherein the weight ratio of isothiazolone to glutaraldehyde is about 1:4.
6. A method according to any one of the preceding claims which comprises adding from 0.05 to 1000 ppm of isothiazolone and 0.2 to 4000 ppm of glutaraldehyde.
7. A method according to claim 6 which comprises adding 0.25 to 50 ppm of isothiazolone and 1 to 200 ppm of glutaraldehyde.
8. A method according to any one of the preceding claims for the treatment of an industrial cooling water system.
9. A method according to any one of claims 1 to 7 which comprises adding the glutaraldehyde and isothiazolone to a recirculating back water used for the paper pulping bath.
10. A method according to any one of claims 1 to 7 which comprises adding the glutaraldehyde and isothiazolone directly to the paper pulping bath.
11. A method according to any one of claims 1 to 7 which comprises adding the glutaraldehyde and isothiazolone to a holding tank containing moist pulp.
12. A method according to any one of claims 1 to 7 which comprises adding the glutaraldehyde and isothiazolone in combination with a chemical additive which is added to the paper pulping bath.
13. A method according to claim 12 wherein the chemical additive is starch, titanium dioxide, a de-foamer, a size, a wet strength resin, a dispersant or retention aid, a filled or optical brightening agent.
14. A method according to claim 1 substantially as hereinbefore described.
15. A composition suitable for addition to an aqueous system which comprises isothiazolone and glutaraldehyde in a weight ratio from 1:1 to 1:10.
16. A composition according to claim 15 wherein the weight ratio is from 1:3 to 1:5.
17. A composition according to claim 16 wherein the weight ratio is about 1:4.
18. A composition according to any one of claims 15 to 17 which contains from 1 to 15% by weight of isothiazolone and glutaraldehyde, taken together.
19. A composition according to claim 18 which contains from 7.5 to 12.5% by weight of isothiazolone and glutaraldehyde, taken together.
20. A composition according to any one of claims 15 to 19 which is in the form of an aqueous solution optionally containing a stabilising agent for the isothiazolone.
21. A composition according to any one of claims 15 to 20 which also contains a chemical additive for a paper pulping bath.
22. A composition according to claim 21 wherein the chemical additive is starch, titanium dioxide, a de-foamer, a size, a wet strength resin, a dispersant or retension aid, a filler or an optical brightening agent.
23. A composition according to any one of claims 15 to 19 which also contains paper pulp.
24. A composition according to claim 15 substantially as hereinbefore described.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB08310532A GB2118925B (en) | 1982-04-19 | 1983-04-19 | Biocide |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8211229 | 1982-04-19 | ||
GB08310532A GB2118925B (en) | 1982-04-19 | 1983-04-19 | Biocide |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8310532D0 GB8310532D0 (en) | 1983-05-25 |
GB2118925A true GB2118925A (en) | 1983-11-09 |
GB2118925B GB2118925B (en) | 1985-06-26 |
Family
ID=26282583
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08310532A Expired GB2118925B (en) | 1982-04-19 | 1983-04-19 | Biocide |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2118925B (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0261607A2 (en) * | 1986-09-26 | 1988-03-30 | Nalco Chemical Company | Biocides for treating industrial waters, particularly flue gas desulfurization scrubber sludge |
EP0337624A2 (en) * | 1988-04-11 | 1989-10-18 | Rohm And Haas Company | Control of oilfield biofouling |
WO1991007090A1 (en) * | 1989-11-16 | 1991-05-30 | Henkel Kommanditgesellschaft Auf Aktien | Combatting slime-forming microorganisms |
DE4007227A1 (en) * | 1990-03-07 | 1991-09-12 | Henkel Kgaa | Control of bio-slimes |
EP0614079A2 (en) * | 1993-03-03 | 1994-09-07 | W.R. Grace & Co.-Conn. | A method of directly monitoring the concentrations of microbiocides in aqueous systems |
EP0631723A1 (en) * | 1993-05-28 | 1995-01-04 | Zeneca Inc. | Protection of isothiazolinone biocides from free radicals |
US5656177A (en) * | 1993-11-30 | 1997-08-12 | Chemische Fabrik Stockhausen Gmbh | Oil-in-water emulsions as substitutes for microbicides (biocides) in water carrying systems |
EP0789595A1 (en) * | 1994-11-04 | 1997-08-20 | BetzDearborn Inc | Synergistic biocidal combinations |
EP0991485A1 (en) * | 1997-03-31 | 2000-04-12 | Fibermark, Inc. | Metal fiber sheet and method of making same |
EP1243695A1 (en) * | 1997-03-31 | 2002-09-25 | Fibermark, Inc. | Metal fiber/metal powder sheet and process for making same |
-
1983
- 1983-04-19 GB GB08310532A patent/GB2118925B/en not_active Expired
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0261607A2 (en) * | 1986-09-26 | 1988-03-30 | Nalco Chemical Company | Biocides for treating industrial waters, particularly flue gas desulfurization scrubber sludge |
EP0261607A3 (en) * | 1986-09-26 | 1989-05-10 | Nalco Chemical Company | Biocides for treating industrial waters, particularly flue gas desulfurization scrubber sludge |
EP0337624A2 (en) * | 1988-04-11 | 1989-10-18 | Rohm And Haas Company | Control of oilfield biofouling |
EP0337624A3 (en) * | 1988-04-11 | 1991-02-06 | Rohm And Haas Company | Control of oilfield biofouling |
WO1991007090A1 (en) * | 1989-11-16 | 1991-05-30 | Henkel Kommanditgesellschaft Auf Aktien | Combatting slime-forming microorganisms |
DE4007227A1 (en) * | 1990-03-07 | 1991-09-12 | Henkel Kgaa | Control of bio-slimes |
EP0614079A3 (en) * | 1993-03-03 | 1995-07-05 | Grace W R & Co | A method of directly monitoring the concentrations of microbiocides in aqueous systems. |
EP0614079A2 (en) * | 1993-03-03 | 1994-09-07 | W.R. Grace & Co.-Conn. | A method of directly monitoring the concentrations of microbiocides in aqueous systems |
EP0631723A1 (en) * | 1993-05-28 | 1995-01-04 | Zeneca Inc. | Protection of isothiazolinone biocides from free radicals |
US5656177A (en) * | 1993-11-30 | 1997-08-12 | Chemische Fabrik Stockhausen Gmbh | Oil-in-water emulsions as substitutes for microbicides (biocides) in water carrying systems |
EP0789595A1 (en) * | 1994-11-04 | 1997-08-20 | BetzDearborn Inc | Synergistic biocidal combinations |
EP0789595A4 (en) * | 1994-11-04 | 2000-11-02 | Betzdearborn Inc | Synergistic biocidal combinations |
EP0991485A1 (en) * | 1997-03-31 | 2000-04-12 | Fibermark, Inc. | Metal fiber sheet and method of making same |
EP0991485A4 (en) * | 1997-03-31 | 2001-08-08 | Fibermark Inc | Metal fiber sheet and method of making same |
EP1243695A1 (en) * | 1997-03-31 | 2002-09-25 | Fibermark, Inc. | Metal fiber/metal powder sheet and process for making same |
US6517675B2 (en) | 1997-03-31 | 2003-02-11 | Fibermark, Inc, | Process for making metal fiber/metal powder sheet |
Also Published As
Publication number | Publication date |
---|---|
GB8310532D0 (en) | 1983-05-25 |
GB2118925B (en) | 1985-06-26 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
732E | Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977) | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20020419 |