GB2027344A - Herbicidal formulation - Google Patents
Herbicidal formulation Download PDFInfo
- Publication number
- GB2027344A GB2027344A GB7829989A GB7829989A GB2027344A GB 2027344 A GB2027344 A GB 2027344A GB 7829989 A GB7829989 A GB 7829989A GB 7829989 A GB7829989 A GB 7829989A GB 2027344 A GB2027344 A GB 2027344A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bifenox
- mecoprop
- phytotoxic
- salt
- ester
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
Classifications
-
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
-
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives thereof
Abstract
A post-emergent method of controlling broadleaf species of weeds in areas of cereal crop growth which involves the application of a combination of bifenox: <IMAGE> and mecoprop: <IMAGE> or a non-phytotoxic salt or ester thereof, to the area in question.
Description
SPECIFICATION
Herbicidal formulations
This invention relates to novel herbicidal formulations of particular value in the post-emergent treat- ment of cereal crops to control broadleaf weeds, and also embraces within its scope methods of control of such weeds by application of the novel formulations.
Heretofore, the broadleaf weed species Galium aparine and Matricaria spp. have proved particularly resistant to conventional herbicides causing such damage to winter and spring cereal crops such as wheat, barley, oats and rye.
It has now been discovered by the Applicants that these species of weed are controlled unexpectedly well by application of formulations containing a combination of bifenox:
and mecoprop:
or salts or esters thereof which are non-phytotoxic to cereals, this combination exhibiting synergistic properties in accordance with the well-known "Colby equation" (see Weeds, '5,20-22(1967)).
The preparation of bifenox is described in United
Kingdom Patent Specification No. 1,232,368 and its use as a herbicide in Proc. N.E. Weed. SciConf 1973, 27, 31. Similarly, the preparation of mecoprop is described in United Kingdom Patent Specification
No.820,180 and its use as a herbicide in Proc. 3rd.
Br. Weed Control Conf. 1956,625.
According to the present invention there is provided, a herbicidal formulation which comprises as active ingredients bifenox and mecocrop, or a salt or ester thereof, associated with a non-phytotoxic carrier therefor.
If a salt or ester of mecocrop is utilised it, of course, must be non-phytotoxic towards the cereal crop. The nature of suitable salts and esters will be well known to those skilled in the art.
The formulations of the invention are intended for use as post-emergent herbicides to be applied to the crop preferably between the one-leaf stage and the start of jointing. The amount of the active ingredients to be applied will be determined by crop sensitivity andlor by the severity of the weed problem.
However, in general, the bifenox will be applied at a rate of 0.25 to 3.0 kg. per hextare whereas the mecocrop will be applied at a rate of from 0.5 to 3.0 kg. per hextare (based on the acid equivalent if a salt or ester is used).
In order to simplify manufacture, storage and transport, the herbicidal formulations of the invention will normally be produced in concentrate form intended for dilution in water to the degree necessary to enable the above mentioned application rates to be easily achieved. Such concentrated formulations may contain from 1 to 90 /O preferably 15 to 85%, by weight of active ingredients associated with one or more inert non-phytotoxic carrier(s) therefor. Such formulations will usually be in the form of a wettable powder, an emulsifiable concentrate or an aqueous suspension.
Wettable powders comprise an intimate mixture of the active ingredients, one or more inert carriers and appropriate surfactants. The inert carrier may be chosen from the attapulgite clays, the montmorillonite clays, the diatomaceous earths, kaolins, micas, talcs and purified silicates. Effective surfactants may be found among the sulfonated lignins, the naphthalene sulfonatesand condensed naphthalene sulfonates, the alkyl succinates, the alkylbenzene sulfonates, the alkyl sulfates and nonionic surfactants such as ethylene oxide adducts of phenol.Illustrative of wettable powders falling within the scope of the invention are those having the following composition:
Wettable Powders
% by weight
Bifenox 1 to 73 Mecoprop* 2 to 79
Surfactant 1 to 10 Dispersing Agent Oto 10
Anticaking agent 0 to 10
Inertcarrier(s) to 100
* based on acid equivalent
Emulsifiable concentrates comprise the active ingredients dissolved in a suitable solvent or suitable solvents together with a surfactant. Suitable surfactants may be chosen from those mentioned above in connection with wettable.powders. Suitable solvents include alkyl substituted benzenes, o-chlorotoluene, heavy aromatic naphthalenes, glycol ethers and cyclic ketones.Typical examples of emulsifiable concentrates falling within the scope of the invention are:
Emulsifiable Concentrates
% weightivolume
Bifenox 1 to 55 Mecoprop 2 to 60
Surfactant(s) 2 to 10
Co-solvent 0 to 40
Solvent to 100
Alternatively, the herbicidal formulation of the invention may be formed by mixing the two active ingredients in a spray tank just prior to use, the water
thus acting as a non-phytotoxic carrier. It is to be
clearly understood that such so-called "tank mixes"
are embraced within the scope of the formulations of the invention.
In both the concentrate and dilute formulation
cases, the ratio of bifenox to mecoprop will lie in the
range 1:2to6:1, preferably from 1:2 to 1:1.
The following non-limitative Examples will further iliustrate formulations in accordance with the invention. In all Examples the amount of mecoprop used
is based on the acid equivalent.
EXAMPLES 7to3 The following wettable powders were prepared in each case have the ingredients shown:
% by weight (1) Bifenox 20
Mecoprop (potassium salt) 40
Sodium lauryl sulphate 3
Sodium lignin sulphonate 3
Precipitated silica 8
Kaolin to 100
% by weight (2) Bifenox 20
Mecoprop (sodium salt) 27
Ethoxylated alkyl phenol 4
Lignosulphonate 3
Fumed Silica 6
Attapulgite to 100
% by weight (3) Bifenox 10
Mecoprop (diethanolamine salt) 25
Sodium salt of condensed
naphthalene sulphonic acids 6
Precipitated silica 10
Sodium alumino silicate to 100
In each Example, the active ingredients were carefully blended with the specified excipients in conventional mixing equipment. The blend was then further milled in a fluid energy mill to a size range of from 1 to 10 microns and finally the mixture was reblended and deaerated prior to being packaged.
EXAMPLES 4 to 6
The following emulsifiable concentrates were prepared having the constituents shown below:
% by weightiby volume (4) Bifenox 15
Mecoprop 30
Calcium dodecylbenzene
sulphonate 3
Alkyl phenoxypolyoxyethylene
ethanols 3
Isophorone 20
Xylene to 100
% by weightiby volume (5) Bifenox 15
Mecoprop ester 20
Alkyl aryl sulphonate 4
Polyoxyethylene triglyceride 4
Cyclohexanone 20
Orthochlorotoluene to 100
% by weightiby volume (6) Bifenox 10
Mecoprop 25
Amine salt of dodecylbenzene sulphonicacid 3
Polyoxyethylene sorbital fatty
esters 4
Isophorone 15
Heavy aromatic naphtha to 100
The active ingredients were added to the appropriate solvent(s) with stirring and optional heating to facilitate solubilisation of the active materials.The surfactants were then added. After solubilisation the solution was filtered to remove insoluble impurities.
EXAMPLE 7
This example illustrates the synergistic effect demonstrated by the combination of the invention when used for control of the broadleaf weeds
Gallium aparine and Matricaria spp.
Winter wheat was sown in France in October at a depth of 3 cm. and at a rate of 150 kg/hectare. The crop was allowed to grow without treatment until the following March, at which time the crop was at growth stage 4-5 (see Plant Pathol., 3 128-9(1954)).
Bifenox and mecoprop were then combined together as a tank mix and sprayed onto the area in which the crop was growing using a knapsack
sprayer at a volume rate per hectare of 300 litres.
Assessments, as weed control ratings, were made between 2 and 5 weeks after application.
TAGFLE % CONTROLOF
Dosage rate Galium Matricaria spp.
glhectare aparine
Bifenox 1000 60 6
Bifenox 1500 71 15
Bifenox + Mecoprop 1000 + 2000 94 87
Bifenox + Mecoprop 1500 + 2000 95 88
Mecoprop 2000 80 50
Claims (3)
1. A herbicidal formulation comprising as active ingredients a combination of bifenox:
and mecoprop:
or a non-phytotoxic salt or ester thereof, associated with a non-phytotoxic carrier therefor.
2. A method of controlling or eradicating broadleaf weeds in an area of cereal crop growth which comprises applying from 0.25 to
3.0 kg/hectare of bifenox together with a 0.5 to 3.0 kg/hectare of mecoprop, or a non-phytotoxic salt or ester thereof, to the area after emergence of the crop.
Priority Applications (38)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7829989A GB2027344A (en) | 1978-07-15 | 1978-07-15 | Herbicidal formulation |
AR277235A AR225418A1 (en) | 1978-07-15 | 1979-07-10 | A SYNERGIC HERBICIDE COMPOSITION TO COMBAT WEEDS IN WINTER CEREAL CROPS. |
SE7906014A SE7906014L (en) | 1978-07-15 | 1979-07-10 | HERBICIDE |
IL57767A IL57767A (en) | 1978-07-15 | 1979-07-10 | Herbicidal method and synergistic compositions comprising a phenoxybenzoic acid derivative and a phenoxyalkanoic acid derivative |
GB7924150A GB2031279B (en) | 1978-07-15 | 1979-07-11 | Herbicides |
DE19792927908 DE2927908A1 (en) | 1978-07-15 | 1979-07-11 | METHOD AND MEANS FOR CONTROLLING WEEDS IN A GRAIN FIELD |
NL7905400A NL7905400A (en) | 1978-07-15 | 1979-07-11 | METHOD FOR CONTROLLING WEEDS IN CEREALS AND HERBICIDES FOR THIS. |
FR7917994A FR2430723B1 (en) | 1978-07-15 | 1979-07-11 | PROCESS FOR THE HERBICIDE TREATMENT OF CEREAL CROPS USING A MIXTURE OF SUBSTITUTED BIPHENYLETHER AND SUBSTITUTED PHENYLALKYLETHER AND COMPOSITIONS THEREFOR |
AT0483979A AT364572B (en) | 1978-07-15 | 1979-07-11 | AGENT FOR CONTROLLING WEEDS IN CEREAL FIELDS |
DK291679A DK160967C (en) | 1978-07-15 | 1979-07-11 | PROCEDURE AND HERBICIDE PREPARATION FOR THE FIGHT AGAINST WEEDS IN THE GROWTH OF A CORN CROP |
RO7998138A RO78004A (en) | 1978-07-15 | 1979-07-12 | ERBICIDA SINERGETICA COMPOSITION |
BE6/46892A BE877675A (en) | 1978-07-15 | 1979-07-12 | HERBICIDE TREATMENT METHOD AND COMPOSITIONS THEREFOR |
CS794899A CS209930B2 (en) | 1978-07-15 | 1979-07-12 | Herbicide means |
NZ190989A NZ190989A (en) | 1978-07-15 | 1979-07-12 | Herbicidal compositions and methods methyl 5-(2,4-dichlorophenoxy)-2-nitrobenzoate and one or more (4-chloro-2-methylphenoxy) alkanoic acid |
TR20527A TR20527A (en) | 1978-07-15 | 1979-07-12 | PROCEDURES FOR FIGHTING WITH HARMFUL HERBS IN CROPS AND HERBISID FORMUELATIONS FOR USE IN THIS PROCEDURE |
ZA00793515A ZA793515B (en) | 1978-07-15 | 1979-07-12 | Herbicides |
GR59590A GR69817B (en) | 1978-07-15 | 1979-07-12 | |
FI792193A FI62204C (en) | 1978-07-15 | 1979-07-12 | FOERFARANDE FOER BEKAEMPNING AV OGRAES PAO VAEXTPLATSEN AV SAEDESVAEXTER OCH VID FOERFARANDET ANVAENDBAR HERBICIDKOMPOSITION |
AU48889/79A AU527751B2 (en) | 1978-07-15 | 1979-07-12 | Synergistic herbicidal composition method |
CH655079A CH641011A5 (en) | 1978-07-15 | 1979-07-13 | Herbicidal treatment process and compositions for this purpose |
MX798191U MX5912E (en) | 1978-07-15 | 1979-07-13 | PROCEDURE TO OBTAIN A SYNERGISTIC HERBICIDE COMPOSITION |
IT49754/79A IT1117178B (en) | 1978-07-15 | 1979-07-13 | IMPROVEMENT IN HERBICIDE COMPOSITIONS |
MA18720A MA18523A1 (en) | 1978-07-15 | 1979-07-13 | HERBICIDE TREATMENT METHOD AND COMPOSITIONS THEREFOR |
BR7904487A BR7904487A (en) | 1978-07-15 | 1979-07-13 | PROCESS TO COMBAT WEED AND HERBICIDE COMPOSITION |
DD79214330A DD144858A5 (en) | 1978-07-15 | 1979-07-13 | METHOD AND MEANS FOR THE CONTROL OF UNCRAFT IN A CEREAL FIELD |
JP8920679A JPS5515483A (en) | 1978-07-15 | 1979-07-13 | Herbicide |
CA331,753A CA1129664A (en) | 1978-07-15 | 1979-07-13 | Method of combating weeds in cereal crops and herbicidal formulations therefor |
PT69919A PT69919A (en) | 1978-07-15 | 1979-07-13 | A method of combating weeds and process for preparing herbicides |
LU81499A LU81499A1 (en) | 1978-07-15 | 1979-07-13 | HERBICIDE TREATMENT METHOD AND COMPOSITIONS THEREFOR |
HU79LI346A HU180832B (en) | 1978-07-15 | 1979-07-13 | Process for selective extirpation of weeds of cereals and for producing synergetic herbicide composition for sellective extirpation of weeds of cereals |
SU792790363A SU860674A3 (en) | 1978-07-15 | 1979-07-13 | Method of fighting weeds |
ES482463A ES482463A1 (en) | 1978-07-15 | 1979-07-13 | Procedure for preparing a synergistic herbicide composition. (Machine-translation by Google Translate, not legally binding) |
BG7944331A BG30615A3 (en) | 1978-07-15 | 1979-07-13 | Herbicide composition and method for weed fighting |
EG424/79A EG13945A (en) | 1978-07-15 | 1979-07-14 | A process for the preparation of a herbicidal formulation comprising known compounds |
PL1979217116A PL116679B1 (en) | 1978-07-15 | 1979-07-14 | Herbicide |
KR7902370A KR830002045B1 (en) | 1978-07-15 | 1979-07-16 | Herbicidal compositions |
IE1325/79A IE48774B1 (en) | 1978-07-15 | 1979-08-08 | Herbicides |
HK738/85A HK73885A (en) | 1978-07-15 | 1985-09-26 | Herbicides |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7829989A GB2027344A (en) | 1978-07-15 | 1978-07-15 | Herbicidal formulation |
Publications (1)
Publication Number | Publication Date |
---|---|
GB2027344A true GB2027344A (en) | 1980-02-20 |
Family
ID=10498452
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7829989A Withdrawn GB2027344A (en) | 1978-07-15 | 1978-07-15 | Herbicidal formulation |
GB7924150A Expired GB2031279B (en) | 1978-07-15 | 1979-07-11 | Herbicides |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7924150A Expired GB2031279B (en) | 1978-07-15 | 1979-07-11 | Herbicides |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS5515483A (en) |
BE (1) | BE877675A (en) |
CA (1) | CA1129664A (en) |
CS (1) | CS209930B2 (en) |
GB (2) | GB2027344A (en) |
ZA (1) | ZA793515B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0231657Y2 (en) * | 1986-10-15 | 1990-08-27 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5635164B2 (en) * | 1973-11-28 | 1981-08-15 | ||
JPS50125030A (en) * | 1974-03-23 | 1975-10-01 |
-
1978
- 1978-07-15 GB GB7829989A patent/GB2027344A/en not_active Withdrawn
-
1979
- 1979-07-11 GB GB7924150A patent/GB2031279B/en not_active Expired
- 1979-07-12 BE BE6/46892A patent/BE877675A/en not_active IP Right Cessation
- 1979-07-12 ZA ZA00793515A patent/ZA793515B/en unknown
- 1979-07-12 CS CS794899A patent/CS209930B2/en unknown
- 1979-07-13 CA CA331,753A patent/CA1129664A/en not_active Expired
- 1979-07-13 JP JP8920679A patent/JPS5515483A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
ZA793515B (en) | 1981-02-25 |
GB2031279A (en) | 1980-04-23 |
JPS5515483A (en) | 1980-02-02 |
CA1129664A (en) | 1982-08-17 |
BE877675A (en) | 1980-01-14 |
GB2031279B (en) | 1983-02-16 |
CS209930B2 (en) | 1981-12-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6444613B1 (en) | Defoliant | |
KR19980701620A (en) | Glufosinate and nitrodiphenyl ether herbicides having a synergistic effect and combinations thereof | |
US20070203025A1 (en) | Defoliant | |
EA008437B1 (en) | Synergistic herbicidal agents | |
US6274535B1 (en) | Defoliant | |
CA2067851C (en) | Herbicidal compositions with increased crop safety | |
US7981838B2 (en) | Defoliant | |
CA1131036A (en) | Herbicidal treatments and formulations | |
GB2027344A (en) | Herbicidal formulation | |
US6413909B1 (en) | Herbicide composition for control of rye grass and vetch in preplant burndown | |
CZ291286B6 (en) | Novel herbicidal agents containing 4-benzoylisoxazoles and aclonifen | |
CS254350B2 (en) | Stabilized liquid herbicide | |
US4645526A (en) | Herbicidal agents | |
EP0101168B1 (en) | Herbicidal mixtures | |
EP0275556B1 (en) | Herbicidal composition | |
HRP960590A2 (en) | Herbicidal system | |
US4017296A (en) | Phosphonates for control of bindweed | |
US4392883A (en) | Herbicidal composition and process | |
IE48774B1 (en) | Herbicides | |
GB2100128A (en) | A herbicidal composition | |
JPH0510323B2 (en) | ||
JPS63179805A (en) | Herbicidal composition | |
DK156753B (en) | FUNGICIDE AGENT CONTAINING A MIXTURE OF ((1,2-ETHAN-DIYLBIS (CARBAMODITHIOATO)) (2 -)) - MANGANE AND A PYRIMIDINE METHANOL, AND PROCEDURES FOR REDUCING FUNGUS INFECTIONS IN CORN CROPS | |
EP0210533A1 (en) | Herbicidal mixtures | |
JPS6253908A (en) | Herbicidal composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |