WO1995015692A1 - Nonphytotoxic aqueous polysulfide contact fungicides and their use - Google Patents

Nonphytotoxic aqueous polysulfide contact fungicides and their use Download PDF

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Publication number
WO1995015692A1
WO1995015692A1 PCT/US1994/013818 US9413818W WO9515692A1 WO 1995015692 A1 WO1995015692 A1 WO 1995015692A1 US 9413818 W US9413818 W US 9413818W WO 9515692 A1 WO9515692 A1 WO 9515692A1
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WIPO (PCT)
Prior art keywords
composition
solution
volume
water
sulfur
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Application number
PCT/US1994/013818
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French (fr)
Inventor
Jorge Miller
Alberto Kling
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Punto Quimica Ltda.
Priority date (The priority date 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 date listed.)
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Publication date
Application filed by Punto Quimica Ltda. filed Critical Punto Quimica Ltda.
Priority to EP95903660A priority Critical patent/EP0732877A4/en
Priority to AU12641/95A priority patent/AU1264195A/en
Publication of WO1995015692A1 publication Critical patent/WO1995015692A1/en

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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N59/00Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/02Sulfur; Selenium; Tellurium; Compounds thereof

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Inorganic Chemistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Lime-sulfur solutions are used to make effective aqueous polysulfide contact fungicides useful for application to plants.

Description

NONPHYTOTOXIC AQUEOUS POLYSULFIDE CONTACT FUNGICIDES AND THEIR USE
Field of the Invention
Stable aqueous polysulfide compositions are useful fungicidal compositions for plants.
Background Sulfur has many allotropic forms. When sulfur is vapor vaporized at a high temperature and quenched in carbon disulfide, a linear chain of sulfur forms; such sulfur chain is insoluble in carbon disulfide. The same happens when acid is added to calcium polysulfide; part of the sulfur formed in also linear and insoluble in carbon disulfide.
Normal sulfur, S8, is soluble in carbon disulfide and is a closed ring octahedron. When hydrogen end bonds are present, they prevent ring closure, except when the linear polysulfidric molecule is too long, where it can break in to S8 and hydrogen sulfide or short polysulfides. Eventually all linear sulfur reverts to S8.
Sulfur and polysulfides are effective contact fungicides. Polysulfides are more effective than sulfur alone; calcium polysulfide (lime-sulfur) is most effective, but has a disadvantage in being phytotoxic in view of its high alkalinity. The active fungicidal ingredient in lime-sulfur is actually the polysulfide ion.
Unfortunately, the polysulfide ion, even a double sulfur sulfide ion, decomposes to hydrogen and free sulfur, thus decreasing its fungitoxic properties. According to Kirk and Othmer's "Encyclopedia of Chemical Technology", Third edition, Vol. 22, p. 122, except for hydrogen sulfide, the sulfanes (H2SX) "have had no practical utility." "Individual hydrogen polysulfides have been characterized from H2S2 up to at least H2S8. They are of no commercial utility by themselves...". Lime-sulfur is prepared, e.g., by boiling together one part by weight of stone lime, two parts by weight of ground sulfur, and eight parts by weight of water to obtain a water soluble mixture of calcium pentasulfide (CaS5) , calcium tetrasulfide (CaS4) , calcium thiosulfate (CaS202) and insoluble calcium sulfite (which can be removed by filtering to obtain a lime-sulfur solution) .
By adding acid to the lime-sulfur solution, pentasulfhydric acid (HSSSSSH) and tetrasulfidric acid (HSSSSH) are formed. These polysulfidric acids rapidly decompose into hydrogen sulfide and colloidal sulfur which, in time, crystallizes to octasulfide (S8). Summary of the Invention
An object of this invention is to find and to prepare a polysulfide fungicide comprising polysulfide ions protected from losing their ionic characteristic and their fungitoxic properties. A further object of this invention is to produce aqueous fungicidal compositions which are not phytotoxic or deleterious to plant leaves. A still further object of the invention is to provide a contact fungicide for plants which can be applied by spraying. Other objects of this invention are apparent from the following details.
Details There are a number of distinct aspects of this invention. One aspect of the invention is an admixture of equal parts by volume of an aqueous li e- sulfur solution containing about 2 gram mols per liter of calcium and an aqueous solution containing about 4.4 gram mols of ammonium salt and about 0.4 gram mol of ammonia per liter. Another aspect of the invention is such a composition which is freshly prepared. A further aspect involves such admixture, particularly one which is freshly prepared, in combination with from about 175 to about 500 parts by volume of water per part by volume of the admixture.
Other aspects of the invention include the use of thus-diluted admixtures as contact fungicides for plants. A significant aspect of the invention is an aqueous fungicidal polysulfidric acid composition which has a basic pH and is not phytotoxic or deleterious to plant leaves, particularly such compositions having a protected polysulfide ion. A still further aspect of the invention involves spraying such an aqueous fungicidal composition on plants as a contact fungicide.
In the context of the disclosure and claims, a number of terms are used which warrant further definition. The term "about" means plus or minus ten percent; the term "polysulfidric acid" means a compound having a chain of sulfur atoms with a hydrogen atom at each end; the term "protected" means that the polysulfide ion is storage stable under normal ambient conditions for up to 5 days; the term "promptly" means within 5 days, advantageously within less than 4 and preferably within one day; the expression "freshly prepared" means prepared within one day and preferably within four hours.
By adding a water-soluble ammonium salt (rather than acid) to the lime-sulfur solution (filtrate) , the corresponding calcium salt and ammonium polysulfides are formed. When the ammonium salt is, e.g., ammonium nitrate, calcium nitrate and ammonium polysulfides are formed. The pH of the resulting solution is practically neutral, and part of the ammonium polysulfides decomposes, forming ammonium sulfide and free sulfur.
2NH4-S-S-S-S-S-NH4 → 2(NH4)2S + 8S (I) The equilibrium reaction: 2NH4OH + H-S-S-S-S-H → NH4-S-S-S-S-NH4 + 2H20 (II) indicates that, according to the law of mass action, a higher concentration of ammonium hydroxide than for the simple neutralization of the lime-sulfur solution with an ammonium salt is required to preserve the polysulfidric ion. By providing an excess of ammonium hydroxide, in addition to a water-soluble ammonium salt, protection of the polysulfide ion is ensured. The resulting pH of the solution is that of ammonium hydroxide, which is not phytotoxic or deleterious to plant leaves. When ammonium nitrate is the water- soluble ammonium salt employed, the formed calcium nitrate simultaneously serves as a foliar fertilizer. The excess ammonium hydroxide also prevents formation of ammonium hydrosulfide, which has a high vapor pressure and is very toxic. In view of the low dissociation constant of polysulfidric acid and ammonia, ammonium polysulfide hydrolyzes to free ammonia and free polysulfidric acid, which, in turn, partially decomposes as follows: 2H-S-S-S-S-S-H → H-S-S-S-S-S-S-S-S-S-H + H2S (III) This reaction proceeds until the sulfur chain (without losing its end hydrogen bonds) precipitates out, forming colloidal sulfur with hydrogen bonds at its ends. Such colloidal sulfur maintains its high fungitoxic properties.
The preferred method for fumigation comprises preparing and applying compositions as follows:
Boil together one part by weight of limestone, two parts by weight of ground sulfur and eight parts by weight of water to obtain a water-soluble mixture of calcium pentasulfide, calcium tetrasulfide, calcium thiosulfate and insoluble calcium sulfite. Filter out the calcium sulfite to obtain a filtrate (lime-sulfur solution) .
Mix one liter of lime-sulfur solution containing two gram mols of calcium ions (Ca++) with one liter of a solution containing 4.4 gram mols of ammonium nitrate (NH4N03) and 0.4 gram mol of ammonia (NH3) . This mixture (primary mixture) is made immediately (preferably without any delay whatsoever) prior to dilution. Such mixture is diluted, e.g., with 400 liters of water and sprayed on plants as a contact fungicide. The resulting admixture is particularly useful for peach and other fruit trees where fungi adhere to the trunk.
When the primary mixture (two liters) is diluted with 800 liters of water and applied to rose bushes afflicted with mildew, it is found suitable for controlling the mildew completely without affecting even new-born tender leaves or rose petals. Field trials reflect that such dilution compares favorably with dilutions of one liter of lime-sulfur solution in 100 liters of water, without the phytotoxic effect of the latter.
Immediate application of the diluted primary mixture is more effective than keeping such diluted admixture for more than five days. The diluted primary mixture should be used within 4 (preferably 2 and, most advantageously, 1) days of such dilution.
Maintaining the primary solution without dilution is counterproductive and ill-advised; it increases the size of the polysulfide. Leaves to which the composition is applied thus require higher doses for the same coverage.
Although fungitoxic properties and non- phytotoxicity remain high, compared to those of different wettable sulfur fungicides available on the market, freshly-prepared fungicidal compositions of this invention are even more effective and more economic to use than compositions that have been stored for any period of time. The invention and its advantages are readily understood from the preceding description. Various changes may be made in the method of making and the method of using the compositions, as well as in the compositions themselves, without departing from the spirit and scope of the invention or sacrificing its material advantages. The methods and compositions described herein are merely illustrative of preferred embodiments of the invention.

Claims

WHAT IS CLAIMED IS:
1. A composition comprising an admixture of two aqueous solutions in equal parts by volume: a) a lime-sulfur solution containing about 2 mols per liter of calcium, and b) a solution containing about 4.4 mols of water- soluble ammonium salt and about 0.4 mol of ammonia per liter.
2. A composition of claim 1 which is freshly prepared.
3. A composition which comprises an admixture of from about 175 to about 500 parts by volume of water per part by volume of a composition of claim 2.
4. A composition of claim 3 which is less than 5 days old.
5. A composition of claim 4 which is freshly prepared.
6. A composition which comprises an admixture of about 200 parts by volume of water per part by volume of a composition of claim 2.
7. A composition which comprises an admixture of about 400 parts by volume of water per part by volume of a composition of claim 2.
8. In a method which comprises spraying an effective amount of a contact fungicide on a plant, the improvement wherein the contact fungicide is an admixture of from about 175 to 800 parts by volume of water per part by volume of a composition of claim 2.
9. A method of controlling mildew on a rose bush which comprises applying to the bush an effective amount of a composition of claim 7.
10. An aqueous fungicidal solution of a polysulfidric acid, which solution has a basic pH and is not phytotoxic or deleterious to plant leaves.
11. A solution of claim 10 wherein the polysulfidric acid comprises octasulfide.
12. A solution of claim 10 which comprises a protected polysulfide ion.
13. In a method which comprises spraying a contact fungicide on a plant, the improvement wherein the contact fungicide is a solution of claim 10.
14. A method which comprises: a) boiling together about 1 part by weight of limestone, about 2 parts by weight of ground sulfur and about 8 parts by weight of water to obtain an aqueous composition comprising calcium pentasulfide, calcium tetrasulfide, calcium thiosulfate and insoluble calcium sulfite; b) filtering out insolubles to obtain a lime-sulfur solution; c) adding a sufficient amount of water-soluble ammonium salt to the lime-sulfur solution to form ammonium polysulfides, and adding a sufficient a ount of ammonium hydroxide to the lime-sulfur solution to protect thus-produced polysulfide ion and its fungitoxic properties.
15. A method of claim 14 which further comprises d) diluting the product of step (c) from about 200 to about 400 times with water.
16. A method of claim 15 wherein step (d) is effected promptly after step (c) .
17. An aqueous sprayable polysulfide fungicidal composition which is neither phytotoxic nor deleterious to plant leaves and which is a product of a method of claim 15.
18. An aqueous fungicidal composition which is neither phytotoxic nor deleterious to plant leaves and which is a composition selected from the group consisting of
I. an admixture of two aqueous solutions in equal parts by volume; a) a lime-sulfur solution containing about 2 mols per liter of calcium, and b) a solution containing about 4.4 mols of water-soluble ammonium salt and about 0.4 mol of ammonia per liter, further diluted from about 200 to about 400 times with water;
II. an aqueous fungicidal solution of a polysulfidric acid, which solution has a basic pH; and
III. a composition of claim 17.
19. In a method which comprises spraying an effective amount of a contact fungicide on a plant, the improvement wherein the contact fungicide is a composition of claim 6.
20. In a method which comprises spraying an effective amount of a contact fungicide on a plant, the improvement wherein the contact fungicide is a composition of claim 7.
PCT/US1994/013818 1993-12-10 1994-11-30 Nonphytotoxic aqueous polysulfide contact fungicides and their use WO1995015692A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP95903660A EP0732877A4 (en) 1993-12-10 1994-11-30 Nonphytotoxic aqueous polysulfide contact fungicides and their use
AU12641/95A AU1264195A (en) 1993-12-10 1994-11-30 Nonphytotoxic aqueous polysulfide contact fungicides and their use

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16495093A 1993-12-10 1993-12-10
US08/164,950 1993-12-10

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WO1995015692A1 true WO1995015692A1 (en) 1995-06-15

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AU (1) AU1264195A (en)
WO (1) WO1995015692A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100461586B1 (en) * 2001-12-12 2004-12-13 동원화학 주식회사 The Preparation of Calcium Polysulfides
KR100761889B1 (en) 2006-04-05 2007-10-04 김진철 Pro-environmental disinfection, insecticide, fertilizer liquid hydrate sulfur, its manufacturing methods and its using methods

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE14890E (en) * 1920-06-22 Edward c
US1437838A (en) * 1919-07-24 1922-12-05 Glidden Co Soluble lime-sulphur composition
US1949797A (en) * 1929-07-30 1934-03-06 Kaufmann Hans Process of producing compositions of matter containing sulphur in colloidal distribution
US2119125A (en) * 1935-03-23 1938-05-31 Stauffer Chemical Co Fungicides and insecticides
US2231423A (en) * 1939-12-05 1941-02-11 Shell Dev Spray for vegetation
US2403939A (en) * 1944-05-31 1946-07-16 American Zinc Lead & Smelting Process for treatment of dolomite and high-calcic limestones
US3030263A (en) * 1959-07-23 1962-04-17 Boehringer Sohn Ingelheim Synergistic fungicidal compositions

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE14890E (en) * 1920-06-22 Edward c
US1437838A (en) * 1919-07-24 1922-12-05 Glidden Co Soluble lime-sulphur composition
US1949797A (en) * 1929-07-30 1934-03-06 Kaufmann Hans Process of producing compositions of matter containing sulphur in colloidal distribution
US2119125A (en) * 1935-03-23 1938-05-31 Stauffer Chemical Co Fungicides and insecticides
US2231423A (en) * 1939-12-05 1941-02-11 Shell Dev Spray for vegetation
US2403939A (en) * 1944-05-31 1946-07-16 American Zinc Lead & Smelting Process for treatment of dolomite and high-calcic limestones
US3030263A (en) * 1959-07-23 1962-04-17 Boehringer Sohn Ingelheim Synergistic fungicidal compositions

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, issued 1970, LUK' YANOVA et al., "Chemical Protection of Plum Plantings from Stigmonose in the Spring-Summer Period", Abstract No. 72: 65756g; & SADOVODSTVO (Kiev), 1967, No. 6, pages 115-122. *
FREAR, DONALD E.H., "Pesticide Index", 4th ed., Published 1969, by COLLEGE SCIENCE PUBLISHERS, PA, see pages 45 and 262. *
GOULD, ROBERT, F., "Advances in Chemistry Series", Published 1972, by AMERICAN CHEMICAL SOCIETY (WASHINGTON DC), see page 55. *
See also references of EP0732877A4 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100461586B1 (en) * 2001-12-12 2004-12-13 동원화학 주식회사 The Preparation of Calcium Polysulfides
KR100761889B1 (en) 2006-04-05 2007-10-04 김진철 Pro-environmental disinfection, insecticide, fertilizer liquid hydrate sulfur, its manufacturing methods and its using methods

Also Published As

Publication number Publication date
EP0732877A1 (en) 1996-09-25
EP0732877A4 (en) 1998-04-29
AU1264195A (en) 1995-06-27

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