AU2002319833B2 - Plant treatment composition - Google Patents

Plant treatment composition

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Publication number
AU2002319833B2
AU2002319833B2 AU2002319833A AU2002319833A AU2002319833B2 AU 2002319833 B2 AU2002319833 B2 AU 2002319833B2 AU 2002319833 A AU2002319833 A AU 2002319833A AU 2002319833 A AU2002319833 A AU 2002319833A AU 2002319833 B2 AU2002319833 B2 AU 2002319833B2
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AU
Australia
Prior art keywords
solution
composition
plant
phosphorous acid
treatment composition
Prior art date
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Application number
AU2002319833A
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AU2002319833A1 (en
Inventor
Alastair James Forsyth
Johannes Anthonie Hough
Justin Thomas Roberts
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FORSYTH ALASTAIR
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Individual
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Filing date
Publication date
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Publication of AU2002319833A1 publication Critical patent/AU2002319833A1/en
Assigned to FORSYTH, ALASTAIR reassignment FORSYTH, ALASTAIR Request for Assignment Assignors: HOUGH, JOHANNES ANTHONIE, ROBERTS, JUSTIN THOMAS
Application granted granted Critical
Publication of AU2002319833B2 publication Critical patent/AU2002319833B2/en
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Description

Technical Field
This invention relates to a plant treatment composition in the form of a
phosphorus containing solution. In one embodiment of the invention the
plant treatment composition may comprise a fertilizer. In one particularly
important embodiment of the invention the plant treatment composition
may comprise a composition for treating plant diseases, especially fungi
Background Art
The use of phosphorous acid and phosphites as fertilizers and/or
fungicides are well known. When used as a fungicide the phosphorous
acid is often injected into the trunk of the plant, but it may also be sprayed
onto the leaves of the plant, painted onto the stem and/or applied to the
soil around the plant stem.
One well-known current commercial phosphorous acid trunk injection
solution for use on avocado trees comprises an un-neutralised aqueous
phosphorous acid solution. However, in order to obtain successful
application by injection a large number of holes have to be drilled in each
trunk (up to about 20 holes) and the solution has to be injected in small
quantities at frequent intervals. This is necessary due to the phytotoxicity of the phosphorous acid solution which causes leaf burn if not applied in
this manner. A further problem is that the holes 'bleed' profusely and
secondary infection of the holes becomes a problem. Severe necrosis of
hard wood around the injection sites was also observed.
It is also know to use neutralised aqueous phosphorous acid solutions as
trunk injection solutions. Usually KOH and K2C03 are used to neutralise
such phosphorous acid solutions. The neutralised solutions have reduced
phytotoxicity (less leaf burn) and reduced hole damage.
It has now been found that if a solution comprising a mixture of
phosphorous acid (and/or phosphites) and ethanol is used as a trunk
injection solution in avocado trees, improved uptake and translocation are
obtained.
Disclosure of the Invention
According to the present invention there is provided a plant treatment
composition formed by the mixture of
- a phosphorus compound; and
an organic polar solvent. The plant treatment composition preferably comprises a solution,
preferably with the phosphorus compound being dissolved in the organic
polar solvent.
The solution may comprise a concentrated solution of the phosphorus
compound. Preferably the solution has a concentration from 1 mol.dm"3 to
7.5 mol.dm"3 of the phosphorus compound. More preferably the
concentration is from 3 mol.dm"3 to 7.5 mol.dm"3. Most preferably the
concentration is about 6.1 mol.dm"3.
The phosphorus compound may comprise an acid, preferably a compound
selected from the group consisting of phosphorous acid,
hypophosphorous acid, polyphosphorous acid, polyhypophosphorous
acid, and salts thereof.
Preferably the phosphorus compound comprises phosphorous acid.
The organic polar solvent preferably comprises a solvent for the
phosphorus compound. The organic polar solvent may comprise an
alcohol. The alcohol may include more than one hydroxyl group, but
preferably it includes a single hydroxyl group. Preferably it comprises
ethanol. In one embodiment of the invention the plant treatment composition may
consist of only the phosphorus compound dissolved in the organic polar
solvent and without the presence of a basic compound. This is especially
the case where the pH of the composition does not play an important role
in the application method. If foliar application, for example, is considered,
the pH of the solution may need to be adjusted in order that the
composition has a suitable pH for foliar uptake. In such a case a basic
compound or compounds may have to be added to the mixture.
Alternatively or additionally, the composition may also include one or more
plant nutrients such as macro-nutrients and/or micro-nutrients.
The composition mixture may accordingly include a basic compound
which increases the pH of the composition. The basic compound may
comprise a compound including an alkali metal salt or an alkaline earth
metal salt. In one embodiment of the invention it may comprise a
potassium salt. The potassium salt may comprise K2C03 or KOH. It will
be appreciated that the potassium from the potassium salt can also serve
as a macro-nutrient.
The pH of the composition may be adjusted as required depending on factors such as the plants to be treated or the method of application of the
plant treatment composition. If foliar application is contemplated, the pH
of the composition should be suitable for foliar uptake. Usually this is at a
pH from about 5 to 7. Preferably the pH is from about 6 to 7. Most
preferably it is about 6.5. In the case of trunk injection or drench
applications the pH should usually be between about 0.5 and about 9.
Preferably the pH is from about 4 to 8. Most preferably it is about 6.5.
A plant nutrient such as a source of nitrogen may also be added. The
nutrient may comprise urea, ammonium nitrate, potassium nitrate,
magnesium nitrate or calcium nitrate.
The composition may also include water. Water may be added in cases
where a compound such as a basic compound and/or nutrient is added
which is not soluble in the polar organic solvent, but which is soluble in
water, or where such compound is added in such an amount that it does
not fully dissolve in the organic solvent and where water is required to
substantially fully solubilise the compound.
The volume percentage of water can vary greatly but ideally it may be at
about 39.5%. The plant treatment composition may also include a surfactant, especially
in the case where an organic polar solvent and water are included in the
composition. The surfactant may be added to ensure that a monophasic
solution forms.
The surfactant may comprise any suitable surfactant, and in one
embodiment of the invention it may comprise propylene glycol.
It will be appreciated that the composition of the plant treatment
composition is expressed in terms of the starting materials used in the
composition. It will be appreciated that in certain cases the phosphorus
compound, the polar organic solvent and other compounds of the mixture
such as a basic compound or nutrients may react with each other to form
reaction products and/or they may dissolve to form dissolved species. For
example where the composition includes a mixture of phosphorous acid
(H3PO3); ethanol, potassium carbonate (K2C03) and water, dissolved
species of, KH2P03, K2HP03, as well as salts of the potassium and the
ethanol may form.
A source of boron may also be added.
The composition may be buffered. Preferably an imidazole and hydrochloric acid buffer is added.
The plant treatment composition may comprise a fertiliser.
In a preferred embodiment of the invention the plant treatment
composition may be used for treating plants against plant diseases.
Preferably the plant treatment composition comprises a fungicide.
Preferably it comprises a fungicide suitable for use against Oomycetes,
preferably for use against Peronosporales, preferably for use against
Phvtophthora, and Pvthium and Plasmopara species.
According to another aspect of the present invention there is provided a
method of preparing a plant treatment composition comprising the step of
mixing together:
a phosphorus compound; and
an organic polar solvent.
Other compounds, in the amounts and ratios as indicated above may also
be added to the mixture.
According to another aspect of the present invention there is provided a
plant treatment composition prepared by the method substantially as described hereinabove.
The invention also relates to the use of the plant treatment composition
substantially as described hereinabove for treating plants or a locus,
especially a locus where plants are cultivated or are to be cultivated.
Preferably the plant treatment composition is used as a fungicide.
Alternatively or additionally the composition may be used as a fertiliser.
The composition may be applied to the plants, for example by spraying the
plants (preferably spraying the foliage of the plants), painting the stems or
drenching their roots. Preferably the solution is injected into plants, and
preferably into the stems of plants.
The invention also relates to a method of treating a plant or a locus
comprising applying to the plant or locus the plant treatment composition
substantially as described hereinabove.
The invention will now be further described by means of the following non-
limiting examples: Example 1
Composition with surfactant in the form of propylene qlvcol
Ethanol (95% ethanol, 5% methanol) in an amount of 200ml was
introduced into a beaker. The ethanol was stirred and 505g of dry
phosphorous acid (99% purity) was added to the ethanol. The solution
was stirred until almost all the phosphorous acid dissolved.
Anhydrous potassium carbonate (99,5% purity) in an amount of 440g was
slowly added to the solution in order to maintain the temperature below
65°C. The potassium carbonate did not fully dissolve. The mixture was
thoroughly stirred and 395ml water was then slowly added thereto. This
mixture was thoroughly stirred until there was no further effervescence.
Two layers formed.
Propylene glycol (surfactant) in an amount of 130ml was then added to the
mixture under constant stirring. A green dye in the form of 0,005g
Hexacol Acid Green dissolved in 5ml of water was then added to provide a
monophasic solution with a green colour.
The resultant solution had a pH of about 6.5 and a specific gravity of about 1 ,322 g/ml.
Example 2
Composition without surfactant (propylene glvcol)
Ethanol (95% ethanol, 5% methanol) in an amount of 200ml was
introduced into a beaker. The ethanol was stirred and 505g of dry
phosphorous acid (99% purity) was added to the ethanol. The solution
was stirred until almost all the phosphorous acid dissolved.
Water in the amount of 462ml was then added to the solution, which was
stirred until all phosphorous acid had dissolved.
Anhydrous potassium carbonate (99.5% purity) in an amount of 320g was
slowly added to the solution in order to maintain the temperature below
approx. 65°C. Once all the potassium carbonate had been added, the
solution was stirred until no more effervescing occurred. A monophasic
solution was obtained.
Lastly a dye, in the form of Hexacol Acid Green, in the amount of 0,005g
dissolved in 5ml water was added to the solution. The resultant solution had a pH of about 3.0 and a specific gravity of about
1.31g/ml.
Example 3
Comparison with aqueous phosphorous acid solution
1. Preparation of aqueous phosphorous acid solution.
Phosphorous acid flakes (99% purity) in the amount of 205g, was
dissolved in 300ml water.
Anhydrous potassium carbonate (99.5% purity) in an amount of
169g was slowly added to the solution to limit the amount of
effervescing. The solution was stirred until no further effervescing
was observed.
Potassium hydroxide flakes (90% purity) in an amount of 122g was
slowly added to the solution. The solution boiled due to the
exothermic reaction. This was also stirred until all had dissolved. Urea low biuret (46% nitrogen mass/mass) in the amount of 10g
was then added and dissolved.
A buffering system in the form of imidazole/hydrochloric acid buffer
(3.5g imidazole/2.43g hydrochloric acid 32%) was then introduced
into the solution.
A dye in the form of 0,005g Hexacol Acid Blue, dissolved in 5ml
water was then added to the solution.
The volume of the solution was then topped-up with water to 1
000ml.
The resultant solution had a pH of about 7.2 and a specific gravity
of about 1 ,24g/ml.
2. Application
The aqueous solution and a solution according to example 1 was
each applied to four different avocado trees of the Pinkerton
cultivar. The trees were about 8 years old with a height of about
4.0m and a diameter of about 4.0m. The trunk diameters were
about 200mm and the trees had a slight woodiness which indicated that they were mildly affected by root rot.
Four injection holes were provided in each tree at a height of about
100 to 150mm above ground level. Each hole was about 30mm
deep and had a diameter of 4.8mm. The holes were angled
downwards at 20 to 30° to the horizontal.
The aqueous solution was applied in an amount of 80ml per tree
thus providing a dose of 1 ,0g phosphorous acid per square meter of
tree area (calculated as height x width).
The ethanol solution of example 1 was applied in an amount of
20ml per tree providing a dose of 0,625g phosphorous acid per
square meter of tree area (calculated as height x width).
The trees were injected on 8 March 2000 and fruit were sampled at
14, 28 and 42 days after injection to determine phosphorous acid
residue therein.
Results
The phosphorous acid residues (mg/kg) in duplicated analyses of
the flesh of the avocado fruit were as follows:
Discussion
With the ethanol solution according to the invention the
phosphorous acid moved into the fruit much quicker than in the
case with the aqueous solution, that is despite the fact that the
aqueous solution was applied at a higher dosage rate of
phosphorous acid. Accordingly the ethanol solution according to
the invention is absorbed at a quicker rate and is more mobile in the
plant compared to the aqueous solution.
Another important aspect is that with the ethanol solution according
to the invention maximum residue of phosphorous acid in the fruit
was obtained at about 28 days, and two weeks later it reduced to
about half of the maximum residue. A maximum allowable
phosphorous acid residue value of 50 ppm in the fruit is generally
considered to be acceptable. It is known that when an aqueous
solution of phosphorous acid (without ethanol) is injected into avocado trees the residue value of the phosphorous acid only dips
below 50ppm after 100 days (the withholding period). Due to the
high mobility of the solutions according to the present invention it is
expected that the withholding period will drop to about 30 days.
The significance of the above is that if it is required to treat a tree
against root rot such treatment could previously not take place
within 100 days of picking when the known aqueous compositions
were used. With a composition according to the present invention
the withholding period can be drastically reduced. It has also been
found that in South Africa late summer rains frequently create
conditions favourable for the development of Phytophthora root rot
and there is a practical need for trunk injections in the
February/March period which falls within the 100 days withholding
period of early maturing fruit. The present invention makes this
treatment possible.
It has also been observed that with the solution according to
example 1 injection holes in the tree trunk healed substantially
completely when they were inspected about 8 months after
injection. This is opposed to the situation where conventional un-
neutralised aqueous solutions of phosphorous acid were used, in which case healing of injection holes is a major problem.
Lower volumes of the composition according to the invention can
also be used and smaller syringes can accordingly be used. Due to
the lower volumes, the injections are a lot quicker. The composition
also causes less damage to trees.
It will be appreciated that many variations in detail are possible without
thereby departing from the scope and spirit of the invention.

Claims (18)

1. A plant treatment composition formed by the mixture of
- a phosphorus compound ; and
- an organic polar solvent.
2. The composition of claim 1 which is a solution wherein the
phosphorus compound is dissolved in the organic polar solvent.
3. The solution of claim 2 wherein the phosphorus compound
comprises a compound selected from the group consisting of
phosphorous acid, hypophosphorous acid, polyphosphorous acid,
polyhyposphorous acid, and salts thereof.
4. The solution of claim 2 wherein the organic polar solvent comprises
an alcohol.
5. The solution of claim 2 wherein the phosphorus compound
comprises phosphorous acid and the solvent comprises ethanol
wherein the phosphorous acid is dissolved.
6. The solution of claim 2 which includes a basic compound which
increases the pH of the solution.
7. The solution of claim 2 which includes a plant nutrient.
8. The solution of claim 2 which includes water.
9. The solution of claim 8 which includes a surfactant.
10. The solution of claim 9 wherein the surfactant comprises propylene
glycol.
11. The plant treatment composition of any one of the preceding claims
which is a fertiliser.
12. The plant treatment composition of any one of claims 1 to 10, which
is a composition for treating plants against plant diseases.
13. A method of preparing a plant treatment composition comprising the
step of mixing together:
- a phosphorus compound; and
- an organic polar solvent.
14. The use of a composition of any one of claims 1 to 10 for treating
plants or a locus.
15. The use of claim 14 wherein the composition is used as a fertiliser.
16. The use of claim 14 wherein the composition is used as a fungicide.
17. The use of any one of claims 14 to 16 wherein the composition is
injected into plants.
18. A method of treating a plant or a locus comprising applying to the
plant or locus the plant treatment composition substantially as
described hereinabove.
AU2002319833A 2001-06-20 2002-06-14 Plant treatment composition Ceased AU2002319833B2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ZA2001/5038 2001-06-20

Publications (2)

Publication Number Publication Date
AU2002319833A1 AU2002319833A1 (en) 2003-05-15
AU2002319833B2 true AU2002319833B2 (en) 2007-02-22

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