Patent Application
20220408725
The application claims the right and priority of the Chinese patent application CN 2020100540594 filed on Jan. 17, 2020, which is incorporated herein in its entirety by reference and for all other purposes.
The invention relates to a new type of defoliant and the application thereof, and specifically to the application of a polyether compound in the preparation of defoliant, belonging to the technical field of pesticides.
Mechanical harvesting of fruit often requires defoliation. The influence of defoliants on the fruit should be minimized, and the fruit abscission rate should also be minimized during defoliation.
Fatty alcohol polyoxyethylene ether (AEO), also known as polyoxyethylene fatty alcohol ether, is the most rapidly developed and most commonly used non-ionic surfactant. This type of surfactant is an ether formed by condensation of ethylene oxide or propylene oxide with aliphatic alcohol, which is represented by the following general formula: RO(CH2CH2O)nH. In the formula, R is generally saturated or unsaturated C12-18 hydroxyl groups, which can be either straight-chain or branched-chain groups; n is the addition number of ethylene oxide, that is, the number of oxyethylene groups in the surfactant molecule. A larger n represents more oxygen on the hydrophilic group of the molecule, which leads to more hydrogen bonds formed with water and better water solubility.
Fatty alcohol polyoxyethylene ether (AEO) is often used as a surfactant in insecticide and fungicide products to increase wettability and penetration and improve performance of the products. As a surfactant, its amount added in the product formula is usually 5-10%, and its concentration is 0.025-0.05%.
The first technical problem to be solved by the invention is to provide an application of polyoxyethylene ether in defoliant or defoliation synergist.
In order to solve the first technical problem of the invention, at least one of a polyether compound shown in Formula I or salts for preparation of a defoliant or a defoliation synergist,
R1O(CH2CHOH)nR2 I
wherein, the R1 is a hydrocarbyl or a phenolic group;
the R2 is —H, —O(CH2CHOH)mH or —O(CH2CH2CHOH)mH;
the n is 1-50, and m is 1-50;
and the salt is preferably a sulphonate or a phosphate.
The salt can be formed based on any position containing a hydroxyl group on R1O(CH2CHOH)nR2.
In a specific embodiment, the cation of the salt is potassium, sodium or ammonium.
In a specific embodiment, the R1 is a C2-50 hydrocarbyl, preferably a C8-22 hydrocarbyl, and more preferably a C12-18 hydrocarbyl.
In a specific embodiment, the R2 is —H;
or the R2 is —O(CH2CHOH)mH, wherein, the n is 2-30, m is 1-30; preferably, n is 2-20, m is 1-20; further preferably, n is 3-9, m is 3-9; and more preferably, n is 3, m is 3;
or the R2 is —O(CH2CH2CHOH)mH, wherein, the n is 2-30, m is 1-30; preferably, n is 2-20, m is 1-20; further preferably, n is 3-9, m is 3-9; and more preferably, n is 3, m is 3.
In a specific embodiment, the n is 2-30, more preferably 2-20, and further preferably 3-9.
In a specific embodiment, the n is 3, 5, 7 or 9, and preferably 5.
For example, R1O(CH2CHOH)3H, R1O(CH2CHOH)5H, R1O(CH2CHOH)7H or R1O(CH2CHOH)9H. R1 is a hydroxyl group, for example, R1 is C12-18.
In a specific embodiment, at least one of R1O(CH2CHOH)3H, R1O(CH2CHOH)7H and R1O(CH2CHOH)9H is used in combination with R1O(CH2CHOH)5H; preferably, R1O(CH2CHOH)7H is used in combination with R1O(CH2CHOH)5H.
At least one of R1O(CH2CHOH)3H, R1O(CH2CHOH)7H and R1O(CH2CHOH)9H is used in combination with R1O(CH2CHOH)5H in any proportion.
In a specific embodiment, the concentration of the R1O(CH2CHOH)nR2 or its salt is 0.2-0.8wt %, preferably 0.5-0.8wt %.
In a specific embodiment, harvesting is performed 3-10 days, preferably 5-7 days, after the defoliant is sprayed.
The second technical problem to be solved by the invention is to provide a defoliant. In order to solve the second technical problem of the invention, the defoliant of the invention contains 0.2-0.8wt %, preferably 0.5-0.8wt %, of the above-mentioned R1O(CH2CHOH)nR2 or its salt and agronomically acceptable additives and solvents.
The solvents can be agronomically acceptable solvents, for example, at least one of water, alcohols (methanol, ethanol, isopropanol, n-butyl alcohol, etc.), xylene, trimethylbenzene, and methylated vegetable oils.
In a specific embodiment, the additive includes a defoamer. The ratio of the mass percentage of the R1O(CH2CHOH)nR2 or its salt to that of the defoamer is 11-99: 0-2, preferably 50-99: 0.01-0.1.
In a specific embodiment, the defoamer is a silicone defoamer or a polyether defoamer.
The beneficial effects are as follows:
1. The invention provides a new defoliant that starts to deliver defoliation effect 3 days after it is applied. The effect reaches the maximum level at the 7th day, and from the 10th to 20th day, some fruits begin to fall down, so the best time of harvesting is recommended to be 7-10 days after the application. The defoliant is safe and effective, free of pollution risk or pesticide residue, and no harm to the environment and organisms. It can be used in combination with ethephon. A dosage 50% less than the normal use can increase the effect of ripening and defoliation, reducing the consumption of chemical pesticides and environmental pollution;
2. The active constituents according to the invention are readily available. R1O(CH2CHOH)nR2 or the salts are commonly seen compounds and frequently used surfactants with good spreading, wetting and permeating effect;
3. R1O(CH2CHOH)nR2 or the salts are readily available and cost-effective chemicals. For example, fatty alcohol polyoxyethylene ether is priced at CNY 8000-12000/t, and the cost is CNY 1.6-2.4/20L of water;
4. In case of proper formulation and working conditions, the defoliant can deliver a favorable effect while exerting a minimized influence on the fruit;
5. The defoliant can be used simply by diluting with water to the corresponding working concentration of compounds.
1# refers to C12-C14 fatty alcohol polyoxyethylene (5) ether.
In order to solve the first technical problem of the invention, at least one of the polyether compound shown in Formula I or salts thereof is used for defoliation.
R1O(CH2CHOH)nR2 I
wherein, the R1 is a hydrocarbyl or a phenolic group;
the R2 is —H, —O(CH2CHOH)mH or —O(CH2CH2CHOH)mH;
the n is 1-50, and m is 1-50;
and the salt is preferably a sulphonate or a phosphate.
The salt can be formed based on any position containing a hydroxyl group on RO(CH2CHOH)nR2.
In a specific embodiment, the cation of the salt is potassium, sodium or ammonium.
In a specific embodiment, the R1 is a C2-50 hydrocarbyl, preferably a C8-22 hydrocarbyl, and more preferably a C12-18 hydrocarbyl.
In a specific embodiment, the R2 is —H;
or the R2 is —O(CH2CHOH)mH, wherein, the n is 2-30, m is 1-30; preferably, n is 2-20, m is 1-20; further preferably, n is 3-9, m is 3-9; and more preferably, n is 3, m is 3;
or the R2 is —O(CH2CH2CHOH)mH, wherein, the n is 2-30, m is 1-30; preferably, n is 2-20, m is 1-20; further preferably, n is 3-9, m is 3-9; and more preferably, n is 3, m is 3.
In a specific embodiment, the n is 2-30, more preferably 2-20, and further preferably 3-9.
In a specific embodiment, the n is 3, 5, 7 or 9, and preferably 5.
For example, R1O(CH2CHOH)3H, R1O(CH2CHOH)5H, R1O(CH2CHOH)7H or R1O(CH2CHOH)9H. R1 is a hydroxyl group, for example, R1 is C12-18.
In a specific embodiment, at least one of R1O(CH2CHOH)3H, R1O(CH2CHOH)7H and R1O(CH2CHOH)9H is used in combination with R1O(CH2CHOH)5H; preferably, R1O(CH2CHOH)7H is used in combination with R1O(CH2CHOH)5H.
At least one of R1O(CH2CHOH)3H, R1O(CH2CHOH)7H and R1O(CH2CHOH)9H is used in combination with R1O(CH2CHOH)5H in any proportion.
In a specific embodiment, the concentration of the R1O(CH2CHOH)nR2 or its salt is 0.2-0.8wt %, preferably 0.5-0.8wt %
In a specific embodiment, harvesting is performed 3-10 days, preferably 5-7 days, after the defoliant is sprayed.
In order to solve the second technical problem of the invention, the defoliant of the invention contains 0.2-0.8wt %, preferably 0.5-0.8wt %, of the above-mentioned R1O(CH2CHOH)nR2 or its salt and agronomically acceptable additives and solvents.
The solvents can be agronomically acceptable solvents, for example, at least one of water, alcohols (methanol, ethanol, isopropanol, n-butyl alcohol, etc.), xylene, trimethylbenzene, and methylated vegetable oils.
In a specific embodiment, the additive includes a defoamer. The ratio of the mass percentage of the R1O(CH2CHOH)nR2 or its salt to that of the defoamer is 11-99: 0-2, preferably 50-99: 0.01-0.1.
In a specific embodiment, the defoamer is a silicone defoamer or a polyether defoamer.
The following description will detail the specific embodiments of the present invention, and the invention will thereby not be limited to the embodiments.
Reagents
C12-C14 fatty alcohol polyoxyethylene (5) ether, purchased from Levima Advanced
Full branched-chain C12 fatty alcohol polyoxyethylene (5) ether, purchased from Sasol (China) Chemical Co., Ltd.
Straight-chain C12-14 fatty alcohol polyoxyethylene (5) ether, purchased from Sasol (China) Chemical Co., Ltd.
Isomeric C13 fatty alcohol polyoxyethylene (5) ether, purchased from Sasol (China) Chemical Co., Ltd.
Glycol analytical reagent
95% ethanol analytical reagent
Silicone-modified defoamer AF-1501, purchased from FTRT CHEMICAL CO., LTD.
40% ethephon solution, purchased from Sichuan Guoguang Agrochemical Co., Ltd.
The constituents of the defoliant in Embodiment 1 is shown in the Table 1 below:
1 Test temperature and humidity
10° C.-20° C., 40%˜70%
2 Reagent description and concentration
The defoliant listed in Table 1 is diluted to a certain extent for application. See Table 2 for the active constituents and dilution factor of the defoliant.
100X, 160X and 400X dilution of the C12-C14 fatty alcohol polyoxyethylene (5) ether refers to 100X, 160X and 400X dilution of the defoliant listed in Table 1 containing an active constituent of C12-C14 fatty alcohol polyoxyethylene (5) ether. 160X+1400X dilution of the C12-C14 fatty alcohol polyoxyethylene (5) ether+40% ethephon refers to 160X dilution of the defoliant listed in Table 1 containing an active constituent of C12-C14 fatty alcohol polyoxyethylene (5) ether and mixture with 40% ethephon subject to 1400X dilution, equivalent to that the mixed solution contains 0.5% of C12-C14 fatty alcohol polyoxyethylene (5) ether and 0.029% of ethephon.
2.2 Plot design
A total of 7 treatment plots (including 1 for control group, with water) are arranged for the test, each including 5 pots.
3 Test method
Spray method. The test reagent is prepared according to the design requirements, and then applied once to each treatment plot by uniformly spraying it onto each pot as per 100 ml/m2 of water consumption, while ensuring consistent spray onto each treatment plot and sufficient spray to cover the whole plant.
4 Investigation
4.1 Investigation time and method
Investigating the total number of treated leaves and fruits of each plant before application of the reagent, and 3 days, 5 days, 7 days, 20 days and 25 days after the application, calculating the defoliation rate and observing the influence on fruits.
Adding fixedly 150 ml of water to each pot each time.
4.2 Calculation method
4.2.1 Absolute value (digital measurement) investigation
According to the investigated data, calculating the defoliation rate as per equation (1), in the unit of percentage (%), rounded to two decimal places.
(1) Defoliation rate (%)=(total number of treated leaves—number of remaining leaves)/total number of treated leaves.
(2) Corrected defoliation rate (%)=(defoliation rate of the treatment plot—defoliation rate of the control group)/(1-defoliation rate of the control group)*100.
If the defoliation rate of the control group <5%, correction is not required; otherwise, the result should be corrected as per equation (2).
(3) Fruit abscission rate (%)=(total number of treated fruits—number of remaining fruits)/total number of treated fruits.
5 Test results and analysis
The defoliation effect on the pepper plants is analyzed through comparison of the results of the pots before and after application of the reagent and the control group.
5.1 Test results
| Number | Date | Country | Kind |
|---|---|---|---|
| 202010054059.4 | Jan 2020 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2020/133508 | 12/3/2020 | WO |
