Aqueous preservative

Details Aqueous preservative Aqueous preservative

2001-04-23

2004-06-22

Paden, Carolyn (Department: 1761)

Food or edible material: processes, compositions, and products

Products per se, or processes of preparing or treating...

With biocide or biostat

C426S321000, C426S331000

Reexamination Certificate

active

06753031

ABSTRACT:

BACKGROUND OF THE INVENTION
The present invention relates aqueous formic acid containing preservative for grass and other agricultural crops, fish and fish products and meat products, having reduced corrosiveness and irritation to skin.
Preserving high moisture grass as silage in anaerobic conditions has been common practice for many years. A fast drop in pH is important to inhibit plant respiration, enzymatic protein breakdown and development of undesired bacteria. The only desired process is the lactic acid fermentation, which stabilises the silage at low pH. The initial drop in pH from approximately 6 to about 4.5 is commonly obtained by adding formic acid at a rate of 2-5 litres/ton grass. Formic acid is the most widespread acid silage preservative mainly due to its efficient acidification and antimicrobial effect, according to J. M. Wilkinson et al. (1966) “Silage in Europe. A survey of 33 countries”, Chalcombe Publications Ltd., Lincoln UK, and McDonald et al. (1991) “The Biochemistry of Silage”, second Ed., Chalcombe Publications, Lincoln UK. Field surveys have shown that formic acid based silage additives have been the most efficient additive for high moisture grass (Nordang, L.Ø. “SurforundersØkelsen 1989-90”, Faginfo, Statens fagtjeneste for landbruket, 6, 1991 and ADAS 1995, “Effect of additives on DM on fermentation”, Grass Farmer, 57, 11). However, 85% formic acid has a high level of corrosion on skin and metal (machinery).
The principles of silage preservation of meat- and fish offals are basically the same as for grass. However, even more stress is put on an efficient acidifier to reduce the pH. This is because offal of animal origin contains very little sugar to produce lactic acid, and the buffering capacity is high.
Mixtures of formic acid and formate salts and also other organic acids (propionic acid and acetic acid and their respective salts) have been developed to reduce the corrosiveness of the acid product. The most successful formulation in terms of efficient preservation and success in major markets has been ammonium tetraformate, comprising about 64% formic acid, about 6% ammonia and the balance being water (EP-411.827B 1). The plain ammonia tetraformate (ATF) has been better than standard formic acid (85%) in terms of corrosion and burns to skin according to P. Westgaard, Journal Buskap og Avdraat, Vol. 37, pp 246-247, 1985. But it is still desired to reduce these negative properties of this efficient preservative. The corrosion on carbon steel has recently been overcome by addition of corrosion inhibitors such as cocobetaine or polyglycoside described in Norwegian Patent Application No. 974200. The skin corrosion is, however, still considered subject to improvements as ATF-type preservatives in this respect have to be labelled with “Corrosion” sign and the risk phrase “Causes burns”.
The problem is to reduce the skin corrosion and at the same time maintain the same acidifying effect and good effect on silage fermentation quality. Just increasing the pH of the preservative might solve the problem of skin corrosion, however, it would produce new problems such as a less efficient preservative.
Known additives for reduction of metal corrosion have not been found to substantially reduce skin corrosion. Addition to preservatives of large amounts of lignosulphonates are claimed to reduce skin corrosion, but this will dilute the preservative and require use of relatively high amounts of preservative to obtain desired effect.
In the patent application WO 96/24247 there is stated that the aim is to obtain a preservative containing formic acid that has reduced corrosiveness on the skin, metal and machinery. A composition is made containing at least one ester of an unsubstituted or substituted benzoic acid with a C
1
-C
9
alcohol or a mixture of such esters and another ester component of an unaromatic C
1
-C
20
carboxylic acid with a C
1
-C
9
alcohol. The preservative further contains at least one C
1
-C
4
carboxylic acid. The preservative may contain 1.5-3 weight % of the ester mixture. This composition is stated to have excellent preservative effect. Data are however not given for corrosiveness with regard to metal or skin.
The main objective of the present invention was to arrive at an improved formic acid containing preservative being less corrosive and irritating to skin.
Another objective was to arrive at a preservative which could be classified as non-corrosive after a four hour skin exposure and thereby bring this type of preservatives from class “Corrosive to skin” (§3.2.5) to “Irritating to skin” (§3.2.6) as defined in Official Journal of the European Communities L 110A, Vol 36, May 4th, 1993 (Annex IV of Commission Directive 93/21EEC).
A further objective was to find a skin corrosion inhibitor which would be effective when applied in minor amounts and thereby avoid dilution or major change of the basic preservative.
In the search for a new solution to the skin corrosion problem related to preservatives it was first decided to concentrate on formic acid containing preservatives, primarily an ATF preservative. It was also essential to maintain the acidifying effect and good effect on silage fermentation quality. Accordingly, reduction of the acidity of the preservative was ruled out. Further checking on known metal anticorrosion agents revealed that their effect on the reduction on skin corrosion was only marginal. Both the corrosion inhibitor cocobetaine and the antioxidant ehtoxyquin were found to be insufficient with regard to reduction of skin corrosion. Thus the mode of action for inhibitors for metal corrosion seemed to be different from what was observed for skin corrosion. One inhibitor for steel corrosion which the inventors found useful to check further was glycerol which has been applied in some preservative in small amounts (0.5%). On skin. however, addition of glycerol to the ATF first seemed to have no effect, but when the amount added was substantially increased, it was surprisingly found that glycerol was able to bring ATF from class “Corrosive to skin” to class “irritating to skin”. The main reason for investigating the effect of glycerol was that it is approved as feed additive in the EU list of additives (E422). Glycerol is further a valuable nutrient for animals and a substitute for several metabolic pathways.
A comprehensive lest program was then started to find the real effect of glycerol compared with other additives to preservatives. These tests proved that glycerol indeed gave a substantial reduction of skin corrosion of the preservative. The necessary amount for obtaining desired reduction in skin corrosion was found to depend on several factors such us the degree of neutralisation of the formic acid with ammonia. But already with addition of more than 0.5 weight % glycerol the skin corrosion started to go down. The upper limit for the glycerol content was found to be more a practical and economic limit in view of the fact that glycerol also is a nutrient. With regard to reduction of skin corrosion, however, it was found that for most cases 1.5 weight % would be sufficient.
SUMMARY OF THE INVENTION
Thus the preservative according to the invention contains ammonium tetraformate or any other combination of formic acid and ammonia and should contain 0.5-5 weight % glycerol.
Preferably the glycerol content in the preservative should be in the range 0.75-1.5 weight %.
The preservative may contain at least one metal corrosion inhibitor such as cocobetaine or alkyl glycoside. The preservative may also contain antioxidant.


REFERENCES:
patent: 4220661 (1980-09-01), Huitson
patent: 4724149 (1988-02-01), Gul et al.
patent: 4978546 (1990-12-01), Haram
patent: 5698246 (1997-12-01), Villamar
patent: 5993875 (1999-11-01), Hjornevik et al.
patent: 0411827 (1993-12-01), None
patent: 2012169 (1979-07-01), None
patent: 0411827 (1991-06-01), None
patent: wo 99/12435 (1999-03-01), None
patent: 93/16603 (1993-09-01), None
patent: 9900023 (1999-01-01), None
patent: 9912435 (1999-03-01), None
Abstract of Norwegian Patent No. 300,441 (Jun. 1997

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