GB2181350A - Contradeglutitious solid herbicidal composition - Google Patents
Contradeglutitious solid herbicidal composition Download PDFInfo
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- GB2181350A GB2181350A GB08525136A GB8525136A GB2181350A GB 2181350 A GB2181350 A GB 2181350A GB 08525136 A GB08525136 A GB 08525136A GB 8525136 A GB8525136 A GB 8525136A GB 2181350 A GB2181350 A GB 2181350A
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- herbicidal composition
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/12—Powders or granules
- A01N25/14—Powders or granules wettable
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
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- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
A contradeglutitious solid herbicidal composition comprising a 1,1'-dimethyl-4,4'-dipyridylium salt and a thickening agent. This composition is difficult to swallow in its original form or even when diluted in a glass of water. The composition does not impair the inherent herbicidal effects and applicability of paraquat.
Description
SPECIFICATION
Contradeglutitious Solid Herbicidal Composition
Background of the invention 1. Field of the invention
The present invention relates to a contradeglutitious solid herbicidal composition (i.e., a herbicidal composition not easy to swallow). More specifically, it relates to a contradeglutitious solid herbicidal composition containing, as a herbicidal agent, a 1,1 '-dimethyl-4,4'-dipyridylium salt (i.e., so-called "paraquat"), which is not easily swallowed even if such a paraquat solution is accidentally or intentionally drunk.
2. Description of the related art
The importance of herbcides or pesticides in modern agriculture is widely recognized and many herbicides or pesticides are in practical use. Herbicides or pesticides practically used must be registered, after being subjected to a severe examination including the toxicity and safety thereof based on the laws and regulations concerned. Accordingly, as long as herbicides or pesticides are properly used according to instructions for use, they will not harm the human body in any way. However, the present status is such that toxic or poisonous accidents caused by a portion of herbicides or pesticides still occur in spite of the fact that the proper handling of herbicides or pesticides and the preventing of injury thereby to the human body has been taught and the dangers of improper usage have been widely announced for a long time.In particular, a herbicide, paraquat, is widely used b-ecause of the strong herbicidal effect and easy applicability thereof, and quite a large number of toxic or poisonous accidents have been caused by the accidental or intentional drinking of paraquat despite clear indications of its toxicity. This is because paraquat has very strong acute toxicity and is commercially available in the form of an aqueous solution having a relatively high concentration.
Paraquat is generally marketed as an about 20% to 30% aqueous solution. When used, the raw paraquat solution is diluted 300 to 1500 times with water and the resultant diluted paraquat solution is generally sprayed as a weed-killer in an amount of 100 to 150 liters per 10 are (i.e., 100 m2). The oral acute toxicity of paraquat is an LD50 of 166 to 217 mg/kg (rat) and it is reported in "Kyukyu Igaku" 4(4), p 399 (1980) that the lethal dose of paraquat for humans is approximately 15 ml of the 20% aqueous solution. On the other hand, it is reported in "Gekkan Yakuji" 25(8), p 147 (1983) that an average amount drunk in one mouthful by an adult human is generally approximately 40 ml.This means that, if a commercially available paraquat solution is accidentally or intentionally drunk, a mouthful of the paraquat solution is sufficient to be lethal to a human.
Various attempts have been made to prevent accidental toxic or poisonous injury caused by paraquat.
For example, odorants or colorants are mixed into the paraquat solutions to prevent accidental drinking by giving it an unpleasant oder or color. However, this is not effective for infants or against intentional drinking. Furthermore, the inclusion of nauseants in the paraquat solutions has been proposed, to rapidly remove the mistakenly drunk paraquat from the stomach and other digestive system prior to the absorbance of paraquat into the body therethrough. However, it is extremely unfortunate that, at present, once paraquat is swallowed, a reliable and effective curing or treatment method is not available, although this depends upon the amount swallowed, even if the paraquat is vomitted at an early stage.
Consequently, although various attempts have been made to solve the above-mentioned problems, an appropriate and effective means has not, as yet, been found. In order to prevent toxic or poisonous accidents caused by the oral intake or paraquat, it is thought that the concentration of commercially available paraquat should be decreased so that a lethal amount is not reached unless a relatively large amount of a paraquat solution is drunk. However, this caused disadvantages in the transportation and storage of paraquat solutions and also impairs the inherent easy handling characteristics of paraquat.On the other hand, it is considered that, when paraquat is marketed in the form of a solid instead of an aqueous solution, the paraquat becomes difficult to drink, toxic or poisonous injuries caused by the accidental intake of paraquat can be prevented, and, furthermore, the transportion and storage thereof are convenient.
However, since paraquat is completely soluble in water, an aqueous solution containing a lethal amount of paraquat is easily prepared from such solid paraquat with a mouthful of water, it would be difficult to prevent to take the poison with suicidal intent.
Summary of the invention
Accordingly, the objects of the present invention are to eliminate the above-mentioned disadvantages of paraquat and to provide a contradeglutitious solid herbicidal composition capable of effectively preventing the occurrence of accidents or injuries from acute poisoning caused by an accidental or intentional intake of paraquat, without impairing the essential characteristics, e.g., strong herbicidal effects and easy applicability, of paraquat.
Other objects and advantages of the present invention will be apparent from the following description.
In accordance with the present invention, there is provided a contradeglutitious solid herbicidal composition comprising a 1,1 '-dimethyl-4,4'-dipyridylium salt and a thickening agent.
Description ofthe preferred embodiments
According to the present invention, since the herbicidal composition is in a solid form and contains a thickening agent, it is difficult to swallow in the solid form itself and, if an amount of the composition corresponding to a lethal dose to human beings is dissolved in a glass of water, only a non-fluidizable mixture, which is difficult to swallow, is obtained. Of course, the present solid herbicidal composition can be changed to an aqueous solution by diluting the composition with a large amount of water. However, since the paraquat concentration of this diluted solution is very low, a lethal amount cannot be ingested unless a remarkably large amount of the diluted solution is drunk. This is particularly difficult and the effects of nauseants can be utilized to decrease the likelihood of death from such ingestion.Furthermore, since the present solid herbicidal composition can be stored and transported in glass and plastic vessels, and since the present solid herbicidal composition can be used on-site by diluting with water, there is no substantial difference between the present solid herbicidal composition and conventional commercially available
paraquat solutions in the transportation, handling, and applicability thereof. When diluting the present solid herbicidal composition with a large amount of water for use on-site, the present solid herbicidal composition becomes a low viscosity solution suitable for spraying.
Furthermore, the solid herbicidal composition according to the present invention may optionally contain, in addition to the essential paraquat and thickening agent, various conventional ingredients such as colorants, odorants, and nauseants, to further improve the safety thereof. In addition, surfactants and other herbicidal active components also can be included in the present herbicidal composition to improve the herbicidal effects and the applicability of the herbicidal composition.
The paraquat usable in the present herbicidal composition is preferably in the form of a solid.
Accordingly, 1,1'-dimethyl-4,4'-dipyridylium salts (e.g., dichloride, dibromide, and bismethylsulfate or the complex salts withjfor example, manganese, iron, urea, thiourea, p-aminophenol, catechol) in the form of crystals can be directly mixed with the thickening agent. However, the industrially or commercially available paraquat solutions also can be used in the preparation of the present solid herbicidal composition by adding a water-absorbing inorganic fine powder to form an apparently water-free fluidizable solid paraquat. Any water-absorbing inorganic fine powder can be used for this purpose so long as the herbicidal effects of the paraquat and the characteristics of the thickening agents are not adversely affected.Examples of such water-absorbing inorganic fine powders are white carbon, diatomaceous earth, finely divided calcium silicate, perlite, calcined kaoline, and zeolite. These can be used alone or in any mixture thereof.
There are no critical limitations to the addition amount of the water-absorbing inorganic fine powder, as long as the paraquat solution can be solidified. For example, in the case of white carbon, an equal amount of the powder can be mixed with 10 times the amount of the water contained in the aqueous paraquat solution.
There are no critical limitations to the paraquat concentration of the present solid herbicidal compositions. However, when the paraquat concentration is too low, only a small dilution ratio of the composition with water is required to obtain the desired concentration when spraying on-site and, therefore, spraying tends to become difficult from the standpoint of both the viscosity and the spraying amount, and the efficiency of the transportation and storage also tends to be decreased. On the other hand, when the paraquat concentration in the present herbicidal composition is too high, the above-mentioned problems do not arise but the allowable safety range tends to become small from the point of view of preventing the possible occurrence of toxic or poisonous accidents.For these reasons, the partically preferably concentration range of the paraquat in the present herbicidal compositions is from about 5% by weight to 40% by weight.
The thickening agents usable in the present invention are those which are capable of increasing the viscosity or forming the gel with the addition of a relatively small amount (e.g., 300 ml or less) of water to the solid herbicidal composition at an ambient temperature in a short period of time. There are no specific limitations to the types of the thickening agents as long as the above-mentioned requirements are fulfilled.
Various natural and synthetic thickening agents can be used in the present invention. Typical examples of such thickening agents are alginic acid salts, propylene glycol alginates; carrageenan, guar gum, modified guar gum, xanthan gum, modified xanthan gum, carboxymethyl cellulose salts, methyl cellulose, hydroxyalkyl cellulose, pectine, locust bean gum, carboxymethyl starch salts, pullulan, polyvinyl alcohol, polyvinyl pyrrolidone, polyacrylic acid salts, and polyacryl amide. These thickening agents may be used alone or in any mixture thereof. Furthermore, various conventional acids or salts also may be used in the present herbicidal compositions to further improve the gellation or thickening characteristics of the present solid herbicidal composition.The addition of inorganic salts to the present herbicidal composition can further improve the gellatin properties of the present herbicidal compositions.
There are no definite concentrations of the thickening agents in the present herbicidal compositions since the concentrations largely depend upon the type of thickening agent and the concentration of the paraquat component. As one practical measure, the thickening agent can be used in an amount such that the herbicidal compositions causes gellation at a paraquat component concentration of 5% by weight or more when the herbicidal composition according to the present invention is diluted with water.That is, when the paraquat concentration of the present solid herbicidal is 5% to 40% by weight, the thickening agent can be added in an amount such that all of the composition becomes a high viscous liquid or gel that cannot be easily swallowed when the present herbicidal compositions is diluted with an equal amount of water, in the case of a paraquat concentration of 5%, to 10 times the amount of water in the case of a paraquat concentration of 40%.
The solid herbicidal composition according to the present invention may further contain, as an optional component, conventional colorants, odorants, nauseants, and the like to improve the safety of the paraquat herbicide as well as surfactants and other herbicidal active components to improve the herbicidal effects.
However, it should be noted that these optional components should be added in such an amount that the herbicidal effects and the other characteristics of the present composition are not adversely affected.
Examples
The present invention will be further explained by, but is by no means limited, to the following
Examples and Test Examples. In the Examples, "parts" and "%" are all by weight unless otherwise specified.
Examples 1 to 7
Paraquat wettable powders were prepared by uniformly mixing and grinding solid paraquat components and other ingredients in the following formulation ratios:
(1) Paraquat dichloride 25 parts
Sodium carboxymethyl-starch 75 parts (Primojel: Matsutani Kagaku Kogyo Co., Ltd.)
(2) Paraquat dichloride 25 parts
Guar gum 35 parts
(Emco gum CSA 200/50: Meyhall Chemical A.G.)
Borax 20 parts
White carbon 20 parts (Carplex(G) #80: Shionogi & Co., Ltd., hereinafter
"white carbon")
(3) Paraquat dichloride 15 parts
Pullulan 60 parts (PullulanQ PF30: Hayashibara Seibutsukagaku
Kenkyusho K.K.)
White carbon 20 parts
Surfactant (Polyoxyethylene nonyl
phenyl ether) 5 parts
(4) Paraquat dichloride 15 parts
Polyvinyl pyrrolidone 60 parts
(Polyvinyl pyrrolidone K-90:Wako Pure Chemical
Industries, Ltd.)
White carbon 20 parts
Surfactant 5 parts
(Polyoxyethylene higher aliphatic alcohol ether)
(5) Paraquat dichloride 15 parts
Carboxymethyl starch 60 parts (SolvitoseQ C-5: Matsutani Kagaku Kogyo Co., Ltd.)
White carbon 20 parts
Surfactant 5 parts
(Polyoxyethylene alkylamine)
(6) Paraquat dichloride 25 parts
Xanthan gum 20 parts (KelzanQ:: Kelco Division of Merck, "Xantham gum"
hereinbelow)
White carbon 30 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
Foaming agent
malic acid 10 parts
sodium bicarbonate 10 parts
(7) Paraquat dimethylsulfate 30 parts
Xanthan gum 40 parts
White carbon 25 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
EXAMPLES 8 to 21
Paraquat wettable powders were prepared by uniformly mixing and grinding a concentrated paraquat solution (i.e., aqueous solution containing 37% by weight of paraquat dichloride) and other ingredients in the following formulation ratios:
(8) Concentrated paraquatsolution 27 parts
Sodium alginate 45 parts (KelginQ:: Kelco Division of Merck)
White carbon 23 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
(9) Concentrated paraquat solution 40 parts
Propylene glycol alginate 20 parts (KimiroidQ: Kimitsu Kagaku Kogyo K.K)
White carbon 35 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
(10) Concentrated paraquatsolution 27 parts
Carrageenan 45 parts (TakaragenQ G50:Takagen Corporation)
White carbon 23 parts
Surfactant 5 parts
(Polyoxyethylene nonlyphenyl ether)
(11) Concentrated paraquatsolution 40 parts
Guargum 15 parts (Emco gum) CSA 200/50)
White carbon 35 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
Nauseant 1 part
(Emetine hydrochloride)
Odorant 4parts (p-Phenethyl alcohol) (12) Concentrated paraquat solution 40 parts
Modified guar gum 15 parts (Jaguar HP-8:Meyhall Chemical AG)
White carbon 35 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
Nauseant 1 part
(Tartar emetic) t3-Phenethyl alcohol 4 parts
(13) Concentrated paraquatsolution 40 parts
Xanthan gum 15 parts
(Kelzan)
White carbon 30 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
Anhydrous sodium sulfate 10 parts
(14) Concentrated paraquatsolution 27 parts
Sodium carboxymethyl cellulose 45 parts (Sunrose()SN 20TC:Sanyo-Kokusaku Pulp Co., Ltd.)
White carbon 23 parts
Surfactant 4parts
(Polyoxyethylene nonylphenyl ether)
(15) Concentrated paraquatsolution 50 parts
Methyl cellulose 10 parts
(Maporose5 M-10000: Matsùmoto Yushi
Seiyaku K.K.)
White carbon 36 parts
Surfactant 4 parts
(Polyoxyethylene nonylphenyl ether)
(16) Concentrated paraquat solution 20 parts
Sodium carboxymethyl starch 57 parts (PrimojelQ White carbon 18 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
(17) Concentrated paraquatsolution 27 parts
Polyvinyl alcohol 45 parts
(PVA 117S:Kuraray Co., Ltd.)
White carbon 23 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
(18) Concentrated paraquatsolution 40 parts
Polyacrylamide 24 parts (Viscomate) NS: Showa Denko K.K.)
White carbon 31 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
(19) Concentrated paraquatsolution 27 parts
Pectin 45 parts
(Genu Pectin BB Rapid Set; the Copenhagen Pectin
Factory Ltd.)
White carbon 23 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
(20) Concentrated paraquatsolution 40 parts
Xanthan gum 14 parts (Kelzan) Locust bean gum 10 parts (MeyprodynQ: Meyhall Chemical AG)
White carbon 31 parts
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
(21) Concentrated paraquat solution 40 parts
Xanthan gum 18 parts (KelzanQ) Diatomaceous earth 37 parts
(Radiolite: Showa Kagaku K.K.)
Surfactant 5 parts
(Polyoxyethylene nonylphenyl ether)
EXAMPLE 22
The following ingredients were dissolved in water.
Paraquat dichloride 30 parts
Guar gum 30 parts
(Emco Gums CSA 200/50)
White carbon 23 parts (CarplexQ #80)
Surfactant 7 parts
(Polyoxyethylene nonylphenyl ether)
Sodium sulfate 10 parts
The resultant solution was granulated by a spray dryer to obtain a granular paraquat wettable powder.
EXAMPLES 23 to 25
Paraquat wettable powders having the following compositions were prepared by uniformly mixing and grinding concentrated aqueous paraquat solution and the other ingredients.
(23) Paraquat dichloride 35 parts
Guar gum 23 parts
(Emco GumQ CSA 200/50)
White carbon 42 parts
(24) Paraquat dichloride 35 parts
Carrageenan 23 parts
(Takaragen: Takagen Corporation)
White carbon 42 parts
(25) Paraquat dichloride 35 parts
Xanthan gum 23 parts (KelzanO) White carbon 42 parts
TEST EXAMPLE 1
A 30 g amount of the solid composition prepared in Example 1 was mixed with 150 ml of water while stirring so as to obtain a mixture having a paraquat concentration of 5%. The mixture became pasty shortly after the water was added. Thus, a pasty mixture, which is difficult to be swallowed, was obtained.
The resultant pasty paraquat composition was then diluted with water in such a ratio that 50 g of the effective component was included in 150 liters of the diluted composition. The diluted herbicidal composition thus obtained was sprayed under pressure to foliage (or stems and leaves) of crabgrass, purple nutsedge, common lambsquarter, pigweed, and barnyard millet, grown in test pots, by using a pressure type atomizer in such an amount that 50 g of the active component per 10 are was applied. Prior to the spraying, a conventional nonionic type spreading agent was added to the herbicidal composition.
During the spraying, no clogging in the spray nozzle of the atomizer occurred. When the herbicidal effects were compared with those of commercially available paraquat solution 5 days after the treatment, no substantial difference was observed.
TEST EXAMPLE 2
A 50 g amount of the solid composition prepared in Example 11 was mixed with 150 ml of water while stirring so as to obtain a mixture having a paraquat concentration of 5%. The mixture became pasty shortly after the water was added. Thus, a pasty mixture, which is difficult to be swallowed, was obtained.
The resultant pasty paraquat composition was then diluted with water in such a ratio that 50 g of the effective component is included in 150 liters of the diluted composition. The diluted herbicidal composition thus obtained was sprayed under pressure onto the foliage of crabgrass, purple nutsedge, common lambsquarter, pigweed, and barnyard millet grown in test pots, by using a pressure type atomizer in such an amount that 50 g of the active component per 10 are was applied. Prior to the spraying, a conventional nonionic type spreading agent was added to the herbicidal composition.
During the spraying, no clogging in the spray nozzle of the atomizer occurred. When the herbicidal effects were compared with those of a commercially available paraquat solution 5 days after the treatment, no substantial difference was observed.
TEST EXAMPLE 3
A 50 g amount of the solid composition prepared Example 13 was mixed with 150 ml of water while stirring so as to obtain a mixture having a paraquat concentration of 5%. The mixture became pasty shortly after the water was added. Thus, a pasty mixture, which is difficult to be swallowed, was obtained.
The resultant pasty paraquat composition was then diluted with water in such a ratio that 50 g of the effective component was included in 150 liters of the diluted composition. The diluted herbicidal composition thus obtained was sprayed under pressure onto the foliage of crabgrass, purple nutsedge, common lambsquarter, pigweed, and barnyard millet grown in test pots, by using a pressure type atomizer in such an amount that 50 g of the active component per 10 are was applied. Prior to the spraying, a conventional nonionic type spreading agent was added to the herbicidal composition.
During the spraying, no clogging in the spray nozzle of the atomizer occurred. When the herbicidal or weeding effects were compared with those of a commercially available paraquat solution 5 days after the treatment, no substantial difference was observed.
TEST EXAMPLE 4
A 40 g amount of the solid composition prepared in Example 15 was mixed with 150 ml of water while stirring so as to obtain a mixture having a paraquat concentration of 5%. The mixture became pasty shortly after the water was added. Thus, pasty mixture, which is difficult to be swallowed, was obtained.
The resultant pasty paraquat composition was then diluted with water in such a ratio that 50 g of the effective component was included in 150 liters of the diluted composition. The diluted herbicidal composition thus obtained was sprayed under pressure onto the foliage of crabgrass, purple nutsedge, common lambsquarter, pigweed, and barnyard millet grown in test pots, by using a pressure type atomizer in such an amount that 50 g of the active component per 10 are was applied. Prior to the spraying, a conventional nonionic type spreading agent was added to the herbicidal composition.
During the spraying to clogging in the spray nozzle of the atomizer occurred. When herbicidal effects were compared with those of a commercially available paraquat solution 5 days after the treatment, no substantial difference was observed.
TEST EXAMPLE 5
The herbicidal effects of the paraquat wettable powders obtained in Examples 23 to 25 were evaluated in an agricultural field. As Reference Examples, a 24% aqueous paraquat solution and a 32% bialaphos liquid agent were used. The weeds used for the test were crabgrass having a height of 25 to 30 cm, smartweed having a height of 50 cm, common lambsquarter having a height of 50 cm, and pigweed having a height of 25 cm.
The area in each test was 1.5 mx 2 m (i.e., 3 m2). The diluted herbicidal composition samples containing 0.3% of a surfactant were sprayed by using a pressure type spray atomizer at an active component amount of 0.5 to 1 kg A.l. (i.e., active ingredient)/ha and at a spraying water amount of 1000 I/ha.
Six days after the spraying, the herbicidal effects were observed according to the following standard 0... No effect
100.. Complete kill
The results are as shown in Table 1. As is clear from the results shown in Table 1, since the grass height at the time of the treatment is relatively large, complete killing was not obtained at a rate of 0.5 kg A.l./ha.
However, in the case of 1.0 kg A.l./ha, good results were obtained and there was no substantial difference between the compositions of Examples 23 and 25 and the conventional paraquat solution.
TABLE 1
Weed control
Sample Rate
Composition No. (kg A.l./ha) Crabgrass Smartweed Lambsquarters Pigweed
Example No. 23 0.5 60 93 70 80
1.0 95 95 100 100
Example No. 24 0.5 85 85 90 93
1.0 98 100 100 100
Example No. 25 0.5 90 90 90 98
1.0 90 100 100 100
Paraquat 0.5 80 75 85 95
1.0 93 98 100 100
Bialaphos 0.5 60 93 70 80
1.0 95 90 100 100 Control O 0 0 0 0 (no treatment)
Claims (10)
1. A contradeglutitious solid herbicidal composition comprising a 1,1 '-dimethyl-4,4'-dipyridylium salt and a thickening agent.
2. A herbicidal composition as claimed in claim 1, further comprising a water absorbable inorganic fine powder capable of converting an aqueous 1,1 '-dimethyl-4,4'-dipyridylium solution into a solid form.
3. A herbicidal composition as claimed in claim 2, wherein said water absorbable inorganic fine powder is at least one member selected from the group consisting of white carbon, diatomaceous earth, finely divided calcium silicate, perlite, calcined kaoline, and zeolite.
4. A herbicidal composition as claimed in claim 1, wherein said thickening agent is at least one agent selected from the group consisting of alginic acid salts, propylene glycol alginates, carrageenan, guar gum, modified guar gum, xanthan gum, modified xanthan gum, carboxymethyl cellulose salts, methyl cellulose, hydroxyalkyl cellulose, pectine, locust bean gum, carboxymethyl starch salts, pullulan, polyvinyl alcohol, polyvinyl pyrrolidone, polyacrylic acid salts, and polyacryl amide.
5. A herbicidal composition as claimed in claim 1,wherein the content of the 1,1 '-dimethyl-4,4'dipyridylium salt in the composition is 5% to 40% by weight.
6. A herbicidal composition as claimed in claim 1, wherein the content of the thickening agent in the composition is such that the composition becomes substantially non-viscous upon the addition of an equal amount to 10 times the amount of water based on the composition and that the composition becomes an easily sprayable low viscosity liquid upon the addition of at least 1500 times the amount of water based on the composition.
7. A herbicidal composition as claimed in claim 1, wherein said composition further comprises a surfactant and a nauseant.
8. A herbicidal composition as claimed in Claim 1 substantially as hereinbefore described.
9. A herbicidal composition as claimed in Claim 1 substantially as hereinbefore described in any one of the specific Examples 1 to 25.
New Claims or Amendments to Claims Filed on 27.2.86
Superseded Claims 1,8,9
New or Amended Claims:
1. A contradeglutitious solid herbicidal composition comprising a 1,1 '-dimethyl-4,4'-bipyridylium salt in a solid form and-a thickening agent.
8. A herbicidal composition as claimed in claim 5, wherein the content of the thickening agent in the composition is such that all of the composition becomes a high viscous liquid or gel that cannot be easily swallowed when the herbidical compositions is diluted with from an equal amount of water, in the case of a paraquat concentration of 5%, to 10 times the amount of water, in the case of a paraquat concentration of 40%.
9. A herbicidal composition as claimed in Claim 1 substantially as hereinbefore described.
10. A herbicidal composition as claimed in Claim 1 substantially as hereinbefore described in any one of the specific Examples 1 to 25.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP1985/000630 WO1987002864A1 (en) | 1985-11-12 | 1985-11-12 | Contradeglutitious solid herbicidal composition |
Publications (3)
Publication Number | Publication Date |
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GB8525136D0 GB8525136D0 (en) | 1985-11-13 |
GB2181350A true GB2181350A (en) | 1987-04-23 |
GB2181350B GB2181350B (en) | 1989-10-18 |
Family
ID=13846631
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8525136A Expired GB2181350B (en) | 1985-11-12 | 1985-11-12 | Contradeglutitious solid herbicidal composition |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0245503A1 (en) |
BR (1) | BR8507308A (en) |
DK (1) | DK361087D0 (en) |
FR (1) | FR2588723B1 (en) |
GB (1) | GB2181350B (en) |
HU (1) | HUT45365A (en) |
WO (1) | WO1987002864A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4874423A (en) * | 1985-10-08 | 1989-10-17 | Merck & Co., Inc. | Solid, herbicidal complexes |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9415290D0 (en) * | 1994-07-28 | 1994-09-21 | Zeneca Ltd | Gel formation |
GB0107651D0 (en) * | 2001-03-27 | 2001-05-16 | Syngenta Ltd | Composition |
CA2791882C (en) | 2010-03-12 | 2018-04-10 | Monsanto Technology Llc | Agrochemical gel compositions |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1395502A (en) * | 1971-07-22 | 1975-05-29 | Ici Ltd | Herbicidal compositions |
GB1506568A (en) * | 1974-03-19 | 1978-04-05 | Ici Ltd | Herbicidal formulations |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4046552A (en) * | 1976-04-15 | 1977-09-06 | Imperial Chemical Industries Limited | Herbicidal compositions of bipyridylium quaternary salts and emetic amounts of s-triazolo pyrimidine derivatives |
GB1507407A (en) * | 1976-04-15 | 1978-04-12 | Ici Ltd | Herbicidal compositions |
JPS56152401A (en) * | 1980-04-28 | 1981-11-26 | Asahi Chem Ind Co Ltd | Powdery herbicidal composition and its preparation |
CN1010654B (en) * | 1984-08-10 | 1990-12-05 | 麦克公司 | The preparation method of the solid-state herbicidal composition of bipyridilium quaternary salt |
-
1985
- 1985-10-21 FR FR8515594A patent/FR2588723B1/en not_active Expired - Fee Related
- 1985-11-12 WO PCT/JP1985/000630 patent/WO1987002864A1/en not_active Application Discontinuation
- 1985-11-12 HU HU861119A patent/HUT45365A/en unknown
- 1985-11-12 GB GB8525136A patent/GB2181350B/en not_active Expired
- 1985-11-12 BR BR8507308A patent/BR8507308A/en unknown
-
1987
- 1987-05-21 EP EP19850905675 patent/EP0245503A1/en not_active Ceased
- 1987-07-10 DK DK361087A patent/DK361087D0/en not_active Application Discontinuation
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1395502A (en) * | 1971-07-22 | 1975-05-29 | Ici Ltd | Herbicidal compositions |
GB1506568A (en) * | 1974-03-19 | 1978-04-05 | Ici Ltd | Herbicidal formulations |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4874423A (en) * | 1985-10-08 | 1989-10-17 | Merck & Co., Inc. | Solid, herbicidal complexes |
Also Published As
Publication number | Publication date |
---|---|
BR8507308A (en) | 1987-11-03 |
GB2181350B (en) | 1989-10-18 |
DK361087A (en) | 1987-07-10 |
FR2588723B1 (en) | 1990-04-13 |
EP0245503A1 (en) | 1987-11-19 |
WO1987002864A1 (en) | 1987-05-21 |
FR2588723A1 (en) | 1987-04-24 |
DK361087D0 (en) | 1987-07-10 |
HUT45365A (en) | 1988-07-28 |
GB8525136D0 (en) | 1985-11-13 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19981011 |