CA2037970A1 - Germicidal composition - Google Patents

Abstract

GERMICIDAL COMPOSITION

Abstract A stabilized germicidal composition in the form of a solution is disclosed which includes a mixed solvent consisting of water and a water-soluble glycol compound having the following general formula:
HO? X ? O - X ? O - Y
wherein X stands for a divalent alkyl group, n is an integer of 0 or more and Y stands for a hydrogen atom, an alkyl group or an acyl group, the weight ratio of the glycol compound to the water being in the range of 95:5 to 20:80; 1-30 % by weight of an isothiazolone compound; and 1-40 % by weight of dibromonitrilepropionamide.

Description

37~
GE~MICIDAL COIIPOSITION
-This invention relates generally to a germicide suitable for preventing growth oE various germs such as yeasts and filamentous fungi in industrial water such as waste water from pulp mills or cooling water for heat exchangers and, more specifically, to a germicidal composition of the above-mentioned type which is stable and has an improved shelf life.
In industrial water such as waste water from paper making steps in pulp-related industries and recirculating cooling water used in various mills, microorganisms such as germs, fungi and bacteria are apt to grow to form slimes which cause various problems. Thus, it is a general practice to incorporate a garmicide in such industrial water.
~ arious germicides have been proposed and some of them are actually used for destroying germs or preventing growth of germs in various fields. Among various germicides, an isothiazolone compound (hereinafter re~erred to as ITZ) is known to be especially effective in preventing the occurrence of slimes. It is also known that conjoint use of ITZ and a dibromonitrilopropionamide thereinafter referred to as NPA) gives excellent synergetic effect. Isothiazolone-type germicides are thus utilized not only as a slime-preventive agent but also as a germ-destroying agent for aqueous paints, machining oils and adhesives.
ITZ-containing germicides, however, have a problem that ITZ is not stable and~ theréfore, the germicidal activity of such germicides is gradually degraded when stored for a long period of time. It is ~nown that ITZ is more stable in a glycol than in other solvents such as ketones and ethers. However, such a glycol solution o~ ITZ is still unstable. For example, non-aqueous solutions containing about 15 % of ITZ in dipropylene glycol completely decomposes in 28 days at 50 C (U.
S. patent No. 3,870,795). If water is incorporated in such a glycol solution, ITZ becomes more unstable and decomposes in much earlier days. NPA is not stable, either. A glycol is known to be a relatively better solvent for NPA than other organic solvents. In an aqueous glycol solution, NPA becomes poorer in stability as compared with in non-aqueous glycol ~ .

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solutions.
The present invention has been made with the above problem of the conventional germicides in view and is contemplated to provide an ITZ-NPA-type germicide having an improved shelf life. In accordance with the present invention there is provided a composition in the form of a solution, comprising:
a mixed solvent consisting of water and a water~
soluble glycol compound having the follo~1ing general formula~
HO-~ X -~ t O - X ~ O Y
wherein X stands for a divalent alkyl group, n is an integer of 0 or more and Y stands for a hydrogen atom, an alkyl group or an acyl group, wherein the weight ratio of said glycol compound to said water is in the range of 95:5 to 20:80;
~ 15 1-30 % by weight of an isothiazolone compound ; dissolved in said mixed solvent; and 1-~0 % by weight of dibromonitrilopropionamide dissolved in said mixed solvent, wherein the weight ratio of said isothiazolone compound to said dibromonitrilopropionamide 20 is in the range of 1:10 to 10:1.
It has been found that when a mixture of a glycol compound and water is used as a solvent for ITZ and NPA, both compounds can be stahilized in the resulting solution. ~'his i5 ;~ very surprising since the presence of water in a glycol compound solvent adversely affects the stability of ITZ and NPA if they are used by themselves.
The present invention will now be described in detail below.
Any isothiazolone compound may be used for the purpose of the present invention as long as it has a germicidal activity. If desired, a mi~ture o two or more isothiazolone compounds may be used. Particularly suited are 3-isothiazolone compounds represented by the following general formula:
~0 CH C
C` N

.
- . . . , : . :
. ' . ~ ' ' ~ . ' _ 8 _ ~ 3 ~

wherein R1 stands for hydrogen or halogen and R2 stands for hydrogen or alkyl. Illustrative of suitable isothiazolone compounds are 2-methyl-3-isothiazolone, 5-chloro-2-methyl-3-isothiazolone, 2-octyl-3-isothiazolone, 2-ethyl-3-isothiazolone and mixtures thereof. Complexes o isothia~olones, such as calcium chloride complexes, magnesium nitrate complexes and iron chloride complexes, may also be usedf though the use of free form isothiazolones is preferred.
NPA to be used in conjunction with ITZ has the Eollowing chemical formula:
Ir Br The present invention is characterized by using a a mixed solvent consisting of water and a water-soluble glycol compound having the following general formula:
HO-~ X 1---~ O - X ~ O - Y
wherein X stands for a divalent alkyl group, n is an integer of 0 or more and Y stands for a hydrogen atom, an alkyl group or an acyl group for obtaining a solution of ITZ and NPA. Examples o~
the divalent alkyl group represented by the symhol X are alkylenes such as ethylene, propylene and butylene. The integer "n" is not specifically limi-ted as long as it gives a water-soluble glycol compound but is generally less than 10. The acyl group represented by the symbol Y is preferably -CO-R in which R
is an alkyl, more preferably a lower alkyl.
Illustrative of sui-table glycol compounds are glycols such as ethylene glycol, diethylene glycol, triethylene glycol, polyethylene glycol (molecular weight of less than about 600), propylene glycol, dipropylene glycol, polypropylene glycol (molecular weight of less than about 800), rnonoalkyl ethers of the above glycols and monoalkyl esters of the above glycols.
The weight ratio of the glycol compound an~ the water in the mixed solvent is in the range of 95:5 to 20:80, preferably in ~he range of 80:20 to 50:50 to provide satisfactory stability of ITZ and NP~. The mixed solvent is .

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used in such an amount that the concentrations of ITZ and NPA in the solution are 1-30 g by weight and 1-40 ~ by weight, respectively, preferably 4-20 % by weight and 4-30 % by weight, respectively.
Solutions of ITZ and NPA in the above mixed solvent are excellent in stability and ITZ and NPA may be prevented from decomposing for a long period of time. Thus, degradation of germicidal activity during storage or transportation is eEfectively prevented.
The following examples will further illustrate the present invention.

Examples 1-15 One or more of ITZs shown in Table 1 were dissolved in the mixed solvents shown in Table 1 together with NPA,. The amounts (parts by weight) of ITZs, NPA, glycol compounds and water are also shown in Table 1 In Table 1, the abbreviations are as follows~

I _ h ~ e Compound:
:~ ITZ-1: 5-Chloro-2-methylisothiazolone ITZ-2: 2-Methylisothiazolone ITZ-3: 2-Octylisothiazolone Glycol Compound:
EG: Ethylene glycol DEG: Diethylene glycol PG: Propylene glycol DGME: Diethylene glycol monomethyl ether ~PG: Dipropylene glycol PEG: Polyethylene glycol (molecular weight: 400) The thus prepared solutions were then allowed to stand at 40 C for 30 days~ The concentrations ~C) of ITZs and NPA in each solution was measured by liquid chromatography 5, 10, 20 and 30 days after the preparation thereof to evaluate the stability thereof in terms of "survival rate (SR)" calculated from , .

- , :
.
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the following equation:

Survival rate = x 100 %
CO
wherein C represents the measured concentration and COrepresents the initial concentration. The results are also shown in Table 1.

Comparative Examples 1-13 The proceduxes of the above Examples 1-13 were repeated in the same manner as described except that the amounts ; of the glycol compounds and water were changed as shown in Table 2. The results are also summarized in Table 2. In Comparative Examples 4-6, the germicidal ingredients were not able to be dissolved in water ~indicated as * in Table 2).

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Claims (3)

1. A composition comprising:
a mixed solvent consisting of water and a water-soluble glycol compound having the following general formula:
HO ? X ? O - X?nO - Y
wherein X stands for a divalent alkyl group, n is an integer of 0 or more and Y stands for a hydrogen atom, an alkyl group or an acyl group, wherein the weight ratio of said glycol compound to said water is in the range of 95:5 to 20:80;
1-30 % by weight of an isothiazolone compound dissolved in said mixed solvent; and 1-40 % by weight of dibromonitrilopropionamide dissolved in said mixed solvent, wherein the weight ratio of said isothiazolone compound to said dibromonitrilopropionamide is in the range of 1:10 to 10:1.

2. A composition according to claim 1, wherein said isothiazolone compound and said dibromonitrilepropionamide are present in amounts of 4-20 % by weight and 4-30 % by weight, respectively and wherein the weight ratio of said isothiazolone compound to said dibromonitrilopropionamide is in the range of 1:5 to 5:1.

3. A composition according to claim 1, wherein said isothiazolone compound is at least one compound selected from those represented by the following general formula:

wherein R1 stands for hydrogen or halogen and R2 stands for hydrogen or alkyl, and complexes thereof.