Patent Grant
7045542
This application is a 371 of PCT/IB00/01489, filed on Oct. 17, 2000.
The invention relates to liquid low-temperature-stable preservatives stable at low temperatures for industrial preservation, in particular for long-lasting protection in water-based products and for imparting biocidal properties to objects or coatings whose surfaces, as experience shows, are frequently attacked by fungi. It further relates to a process for the preparation and use thereof.
Fungal attack is not only visually unappealing, but can, in the case of subsequent growth of lichen or moss, also lead to material damage and a reduction in service life. The attack of objects or coatings applied thereto occurs particularly intensively in areas of high atmospheric humidity, such as, for example, in the food industry sector, in dairies, breweries or on the north faces of buildings. In particular, coatings such as paints, varnishes and renders are affected.
The attempt to solve the above-described problem by adding pulverulent substances to the coating materials used is associated with numerous application disadvantages. The demand for solvent-free or low-solvent preparations led to the development of aqueous dispersions in which known, water-insoluble fungicidal active ingredients were used.
For example, aqueous dispersions based on carbendazim and other active ingredients have been found although, because of the fact that the fungicide carbendazim is sparingly soluble, they are not very stable upon prolonged storage and at relatively high and relatively low temperatures and, in numerous fields of use (e.g. in the cutting fluid sector) cannot be incorporated clearly and homogeneously into the products to be furnished. After standing for a relatively long period precipitates form which are difficult to disperse or cannot be dispersed at all.
To avoid this problem, salts of carbendazim have been used, for example alkylbenzenesulphonate salts thereof, preferably in organic solvents, such as 1,2-propylene glycol.
However, such compositions comprising carbendazim salts likewise displayed the tendency towards precipitations during preparation, storage or transportation. The precipitations occurred at room temperature, but also sometimes only at relatively low temperatures (e.g. +4° C.) or in winter during frost (e.g. at −5° C.). These precipitations are in turn irreversible at low temperatures, i.e. they do not disappear again when room temperature is reached.
The object of the present invention is therefore to render preservatives comprising carbendazim or carbendazim salts stable at low temperatures, it being the aim that this low-temperature stability extends below minus temperatures such as, for example, −5° C., and is retained over a relatively long period, even during storage at such low temperatures.
Surprisingly, the object according to the invention was then achieved by the fact that we have found that stable, homogeneous, low-temperature-stable liquid products based on carbendazim or carbendazim salts can be prepared if the composition comprises, as low-temperature stabilizer, at least one aromatic alcohol and/or at least one aromatic glycol ether and/or at least one pyrrolidone, even small amounts sufficing to obtain this low-temperature stability.
The aromatic alcohols or glycol ethers also improve the antimicrobial/germicidal or preserving action of the preparations, and they are, in particular, antimicrobially active in the vapour phase.
The liquid, low-temperature-stabilized preservative based on carbendazim or a salt thereof according to the invention is therefore characterized in that it comprises, as low-temperature stabilizer, at least one aromatic alcohol or aromatic glycol ether or a pyrrolidone.
Preferred embodiments are the subject of the dependent claims.
Preferred low-temperature stabilizers according to the invention are the aromatic alcohols phenylpropanol and benzyl alcohol and the C6–C10-aryloxy-C2–C6-alkylene glycol ethers classed as aromatic glycol ethers, where the aryl group is, in particular, a phenyl group and independently thereof the alkylene group is, in particular, a C2- or C3-alkylene group.
Particularly preferred low-temperature stabilizers are phenoxypropanols and phenoxyethanol, the phenoxypropanols including 1-phenoxy-3-propanol, 2-phenoxy-1-propanol and 1-phenoxy-2-propanol. Very particular preference is given to phenoxyethanol and mixtures of 2-phenoxy-1-propanol and 1-phenoxy-2-propanol (referred to in the examples as “phenoxypropanols”).
Also suitable are pyrrolidones, N-methyl-pyrrolidone and N-octylpyrrolidone being preferred.
These stabilizers can, for example, be used in exchange or partial exchange for solvents or dispersants used hitherto, such as, for example, 1,2-propylene glycol.
The content of the claimed low-temperature stabilizer in preservatives according to the invention is at least 2% by weight, preferably at least 3% by weight and in particular at least 5% by weight, the maximum content being noncritical if there is complete exchange for media used hitherto. The low-temperature stabilizer according to the invention can be present, for example, in an amount of 10, 15 and 20% by weight, but also of 70, 80 or 90%. It fulfils then not only the function of the low-temperature stabilizer, but also that of the solvent or solubility promoter.
In preferred embodiments, a salt of carbendazim is present in the liquid low-temperature-stabilized preservative according to the invention, preference being given to the alkylbenzenesulphonate salts which have 6 to 18, in particular 10 to 14 and preferably 12, carbon atoms in the alkyl group. A particularly preferred alkylbenzenesulphonate salt of carbendazim is carbendasulf, which can be prepared by reacting carbendazim with dodecylbenzenesulphonic acid (Marlon AS 3-acid) in propylene glycol at about 85° C. The hydrochloride and the hydrobromide of carbendazim are also suitable salts according to the invention.
Because of the higher stability even at low temperatures, the content of fungicide in the preservative remains on a high level, as a result of which biocidal action can likewise be maintained for a long period.
Moreover, because of the possibility of considerably lowering or avoiding the content of diverse solvents and other low-temperature stabilizers, a reduction in the preparation costs of carbendazim-containing products can be achieved.
Therefore, because of the higher low-temperature stability, the preservatives according to the invention have the following advantages over comparable products of the prior art:
The low-temperature stabilizers according to the invention can be used subsequently to or even during the preparation of, for example, the alkylbenzenesulphonates of carbendazim, such as, for example, carbendasulf, as additive, partial replacement or complete replacement of solvents used hitherto, such as, for example, 1,2-propylene glycol etc. This has the advantage that the reaction time and temperature for the preparation of the clear homogeneous solution can be reduced, as a result of which a higher thermal stress (“roasting”) is avoided, which contribute to the decomposition of the alkylbenzenesulphonates. Also as a result of the avoidance of such additional thermal stress, the content of alkylbenzenesulphonate remains comparatively high again and the type and amount of the decomposition products decreases.
The preservatives according to the invention can be used as additives for coatings, for plastic dispersions, in particular those which are film-forming and are based, for example, on polyacrylate, for the treatment of surfaces and materials and for imparting fungicidal properties to paints, varnishes and renders, for container preservation and for material protection and for the preservation of metalworking fluids (concentrates and emulsions).
In combination with further active ingredients, including, for example, algicides and bactericides, the activity spectrum of the preservatives according to the invention can also be extended to further areas.
In practice, the use concentration of the preservative according to the invention in the material to be preserved can be in the range from 0.01 to 10% by weight, in particular 0.05 to 5% by weight and preferably 0.15 to 3% by weight. In coatings, the preservative according to the invention can be used in amounts such that, on an area of 1 m2, 0.01 to 10 g, preferably 4 g, are used.
In addition to carbendazim or carbendazim salts such as carbendasulf, the preservatives according to the invention can comprise other biocidal active ingredients (bactericidal, fungicidal, algicidal and/or virucidal). This produces broad-activity, sometimes synergistically active, products.
Examples of such biocidal active ingredients which may be present in the preservatives according to the invention are
Examples are given below which are intended to illustrate the invention, without signifying any limitation.
By way of example, additives suitable for improving the stability of carbendasulf-containing preparations are described.
The improvement in the stability of carbendasulf-containing preservatives (e.g. low-temperature stability) is possible as a result of the addition of aromatic alcohols or aromatic glycol ethers (5 to 15% of benzyl alcohol, phenoxyethanol, phenoxypropanols).
4% by weight of carbendazim and 6.5% by weight of Marlon AS 3 (amounts given are based on the total weight) were heated in 1,2-propylene glycol to 85° C. After the temperature was reached, the mixture was left to cool to about 60° C. and filtered. The remaining constituents were added to the filtrate, and the mixture was stirred for about 15 minutes. Following seeding with carbendasulf crystals, the mixture was stored in clear glass at −5° C.
Following storage for about 3 months at −5° C. the ranking of the low-temperature stabilization (replacement of 1,2-propylene glycol as previously used solvent for 10% or 15% of stabilizer according to the invention) is as follows:
3-phenylpropanol>phenoxypropanols>N-methyl-pyrrolidone>dipropylene glycol monomethyl ether>1,2-propylene glycol.
After about 15½ months at −5° C. the mixtures have the following precipitate percentages:
Result: An addition of selected stabilizers significantly improves the low-temperature stability of carbendasulf-containing preservatives (control without stabilizer is formulation 1). The improvement compared with 1,2-propylene glycol or dipropylene glycol monobutyl ether is apparent in the case of 10 or 15% phenoxypropanol from a reduction in the amount of precipitate from 50 to 20% or 40 to 0% respectively, and in the case of 10 or 15% 3-phenylpropanol from a reduction in the amount of precipitate from 40 to 10% or 40 to <5% respectively. In the case of N-methylpyrrolidone, a reduction from 50 to 30 and from to 15% respectively is found.
Carbendazim, Marlon AS 3 and propylene glycol (constituents 1 to 3; see table) were heated together to 85° C. with stirring. After this temperature had been reached, the mixture was left to cool to about 60° C. and filtered (very little insoluble matter). The filtrate was combined with the mixture of constituents 4 to 8 (see table) and stirred for about 4 of an hour. After seeding, the examples are stored in clear glass at −5° C., 4° C., 25° C. or 40° C. The results are given in the table below (“Zonenfex” is a salt-free solution of a mixture of 5-chloro-N-methylisothiazolone and N-methylisothiazolone in glycol derivatives):
Result: Suitable stabilizers for increasing the low-temperature stability of preservatives and low-water, carbendasulf-containing preparations are benzyl alcohol, phenoxyethanol and phenoxypropanols.
The following stabilizers are unsuitable: diethylene glycol butyl ether, 1-methoxy-2-propanol, polyglycol 400 and dipropylene glycol.
Background: The preparations according to the invention are purer (lower proportion of decomposition products) and the preparation is more economical than that which was previously possible. The preparation to date requires that the mixture be heated at +85° C. for 4 hours (if the residence time is shorter, the product is insufficiently stable or stable at low temperatures), which leads to the formation of byproducts.
According to the invention, a lower reaction temperature and/or reaction time of significantly less than 1 hour (preferably less than 30 minutes) is sufficient. The components carbendazim and Marlon AS 3 acid have only to be heated in a suitable solvent (e.g. 1,2-propylene glycol) to clear solubility, then cooled and mixed with the other formulation constituents. The carbendasulf solutions according to the invention are inevitably purer (and because of the higher carbendasulf content, more effective) and more economical to prepare.
In the case of formulations B, E and G, the carbendasulf content is generally higher than in the case of the production batches without the stabilizer according to the invention (formulation A).
Carbendazim, Marlon AS 3 and propylene glycol were combined and heated to 85° C., the mixture was left to cool to 60° C. and the remaining ingredients were added (the temperature drops to <40° C.). The mixture was clear, greenish-brown and was filtered. The sample was stored and seeded at −5° C. or 4° C. or 25° C. or 40° C. Further data are given in the table below:
Comparison, the preservative without stabilizer stored at −5° C., 4° C., 25° C.
The biocides were added to the dispersions in an amount of 2%. This high concentration was knowingly chosen in order to see the effect of the preservative more clearly.
Result: After the biocides had been incorporated into four different salt-insensitive dispersion products, no incompatibility was found. All of the mixtures were stable upon storage. The odour and colour of the products were not changed by the preservatives according to the invention. A change in the minimum film-forming temperature (MFT) or the washfastness by the solvent content present in the variant is not evident either.
Both versions of the preservative without stabilizer are compatible with the standard dispersions tested. The incompatibility with the salt-sensitive dispersion has hitherto also been observed in the case of all other similar biocides (because of its specific monomer composition, this dispersion tolerates only salt-free biocides).
Carbendazim, Marlon AS 3 and propylene glycol (constituents 1 to 3; see table) were heated to 85° C. with stirring. After this temperature had been reached, (very little insoluble matter). The filtrate was combined with the mixture of constituents 4 to 7 (see table) and stirred for about ¼ of an hour. After seeding, the samples were stored in clear glass at −5° C., 4° C., 25 and 40° C.
At room temperature, all solutions were clear, yellow-brownish. Storage was in clear glass at −5° C. or 4° C. or 25° C. or 40° C.
Result: After about 30 months at −5° C. or 4° C., the mixtures have the following precipitate percentages:
Result: An addition of phenoxyethanol significantly improves the low-temperature stability of the preservative (formulation P).
The solvent was initially introduced. Carbendazim and Marlon AS 3 were added thereto and stirred. The mixture heated up to 37° C. It was heated to about 80° C., giving a clear, brown solution. The solution was stirred until it had cooled to room temperature. The solution was then filtered with suction over a glass filter with a black belt filter.
Carbendasulf is prepared from carbendazim (black belt filter) and Marlon AS 3 in the ratio 1 mol:1 mol.
The 20% strength and 10% strength solutions were prepared from a more highly concentrated solution by dilution. The individual solutions were seeded with crystals. These solutions were stored in each case at −5° C., 4° C. and 25° C. in clear glass in order to establish the low-temperature stability.
Result: The combination of carbendasulf with stabilizers according to the invention permits the preparation of comparatively highly concentrated carbendasulf solutions, which can be combined with further active ingredients to give broad-activity, sometimes synergistically effective, preparations.
1,2-Propylene glycol was initially introduced, carbendazim and Marlon AS 3 were added thereto and the mixture was stirred. The mixture heated up to 45° C. and became paste-like. It was heated to about 80° C., forming a clear brown solution. The stabilizer was then added. The solution was stirred until it had cooled to room temperature. The solution was then filtered with suction over a glass filter with black belt filter.
Carbendasulf is prepared from carbendazim and Marion AS 3 in the ratio 1 mol:1 mol.
The 20% strength and 10% strength solutions were prepared by dilution. The individual solutions were seeded with crystals. The solutions were each stored in clear glass at −5° C., 4° C., 25° C. in order to establish the low-temperature stability. The data are given in the table below.
Result: The combination of carbendasulf with stabilizers according to the invention permits the preparation of comparatively highly concentrated carbendasulf solutions, which can be combined with further active ingredients to give broad-activity, sometimes synergistically active, preparations.
Carbendasulf solutions with a combination of aliphatic glycols or glycol ethers and stabilizers according to the invention are preferred.
7.45% of carbendazim+12.55% of Marlon AS 3 acid+23.33% of propylene glycol (PLG)+56.67% of phenoxyethanol (POE).
Propylene glycol was initially introduced, the carbendazim was added and, with stirring, Marlon AS 3 was added. The mixture becomes solid and heats up to 45° C. The mixture was heated to 80° C., and the now liquid preparation was admixed with phenoxyethanol and, with stirring, allowed to cool to room temperature, giving a clear brown solution.
50% of 20% strength carbendasulf solution from Example 9 was combined with 10% of Proxel press paste (BIT) and 40% of phenoxyethanol and stirred for about 1 hour, giving a clear deep red solution.
| Number | Date | Country | Kind |
|---|---|---|---|
| 199 51 328 | Oct 1999 | DE | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IB00/01489 | 10/17/2000 | WO | 00 | 4/12/2002 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO01/28332 | 4/26/2001 | WO | A |
| Number | Date | Country |
|---|---|---|
| 0 031 454 | Jul 1981 | EP |
| 0 351 195 | Jan 1990 | EP |
| 2 066 075 | Jul 1981 | GB |
| 9955505 | Nov 1999 | WO |
