In situ mixing and application of hydrocolloid systems for pre- and post harvest use on agricultural crops
View Patent ↗In-situ methods of applying ethylene response manipulation formulations are disclosed. The formulations comprise at least one ethylene response manipulation agent which is at least partially encapsulated, a polyol liquid medium, or a hydrogel medium, or a combination of polyol and hydrogel medium. A preferred ethylene response manipulation agent is 1-methylcyclopropene.
1. An in-situ method of reducing loss of 1-methylcyclopropene (1-MCP) in a modifying plant ethylene response formulation to be applied to at least one target plant in a direct soil application comprising the steps of:
a) mixing or suspending 1-methylcyclopropene (1-MCP) at least partially encapsulated with at least one encapsulant, in a water based medium, to form a 1-MCP control release mixture comprising encapsulated 1-MCP and free 1-MCP,
b) forming a 1-MCP control release liquid formulation from the mixture in a continuous stirred tank system, and
c) immediately spraying the 1-MCP control release formulation, within or less than 1 hour of formulation formation, onto at the least one target plant in a direct soil application, wherein less than 80% by weight gaseous or volatile 1-MCP is released into a headspace of an airtight chamber from the 1-MCP controlled release liquid formulation.
2. The method of claim 1 wherein the formulation comprises from about 0.01 to about 10,000 milligrams by weight of said 1-MCP per liter.
3. The method of claim 1 wherein the formulation is applied at a rate of from about 0.1 gram to about 100 grams of said 1-MCP per hour.
4. The method of claim 1 wherein the encapsulant is cyclodextrin.
5. The method of claim 1 wherein the encapsulant is α-cyclodextrin or modified α-cyclodextrin.
6. The method of claim 1 wherein the encapsulant is β-cyclodextrin or modified β-cyclodextrin.
7. The method of claim 1 wherein the encapsulant is γ-cyclodextrin or modified γ-cyclodextrin.
8. The method of claim 1 wherein a ratio of encapsulated to non-encapsulated 1-MCP can be about 99:1 to about 50:50.
9. The method of claim 1 wherein the formulation further comprises at least one pesticide.
10. The method of claim 9 wherein the pesticide is selected from the group consisting of fungicide, insecticide and biopesticide.
11. The method of claim 1 wherein the formulation further comprises at least one plant growth regulator.
12. The method of claim 11 wherein the plant growth regulator is selected from the group consisting of gibberellic acid, etheral and aminoethoxyvinylglycine.
13. The method of claim 1 wherein the formulation further comprises a surfactant.
14. The method of claim 13 wherein the surfactant is selected from the group consisting of anionic, cationic, nonionic, zwitterionic and ampholytic surfactants.
15. An in-situ method of reducing loss of 1-methylcyclopropene (1-MCP) in a modifying plant ethylene response formulation to be applied to at least one target plant in a direct soil application using an automated combination mixing and spraying equipment comprising the steps of:
a) mixing or suspending 1-methylcyclopropene (1-MCP), at least partially encapsulated with at least one encapsulant, in a water based medium, to form a 1-MCP control release mixture comprising encapsulated 1-MCP and free 1-MCP,
b) passing the mixture into a stirred tank system to form a 1-MCP controlled release liquid formulation, and
c) immediately spraying the volatile 1-MCP control release liquid formulation onto at least one target plant in a direct soil application within or less than 1 hour of formulation formation such that the formulation remains sprayable and wherein less than 80% by weight gaseous or volatile 1-MCP is released into a headspace of an airtight chamber from the 1-MCP controlled release liquid formulation.
16. The method of claim 15 wherein the encapsulant is cyclodextrin.
17. The method of claim 15 wherein the encapsulant is α-cyclodextrin or modified α-cyclodextrin.
18. The method of claim 15 wherein the encapsulant is β-cyclodextrin or modified β-cyclodextrin.
19. The method of claim 15 wherein the encapsulant is γ-cyclodextrin or modified γ-cyclodextrin.
20. The method of claim 15 wherein the formulation further comprises a surfactant.
21. The method of claim 20 wherein the surfactant is selected from the group consisting of anionic, cationic, nonionic, zwitterionic and ampholytic surfactants.
22. An in-situ method of reducing loss of 1-methylcyclopropene (1-MCP) in a modifying plant ethylene response formulation to be applied to at least one target plant in a direct soil application comprising the steps of:
a) mixing or suspending 1-methylcyclopropene (1-MCP) powder encapsulated with at least one encapsulant, in a water based medium, to form a volatile 1-MCP control release liquid formulation comprising encapsulated 1-MCP and free 1-MCP, and
b) spraying the volatile 1-MCP control release liquid formulation onto at least one target plant in a direct soil application within or less than 1 hour of formulation formation such that the formulation remains sprayable and wherein less than 80% by weight gaseous or volatile 1-MCP is released into a headspace of an airtight chamber from the 1-MCP controlled release liquid formulation.
23. The method of claim 22 wherein the formulation further comprises at least one antimicrobial.
24. The method of claim 23 wherein the antimicrobial is selected from the group consisting of chlorine dioxide, sulphur dioxide, thymol, carvacrol, cinnamaldehyde, allyl isothiocyanate, ethanol, oregano extracts, other synthetic or natural occurring flavanols, phenolic compounds and organic acids.
25. The method of claim 22 wherein the formulation further comprises at least one antioxidant.
26. The method of claim 25 wherein the antioxidant is diphenyl amine or ethoxyquin.
27. The method of claim 22 wherein the formulation further comprises at least one plant growth regulator.
28. The method of claim 27 wherein the plant growth regulator is selected from the group consisting of gibberellic acid, etheral and aminoethoxyvinylglycine.
29. The method of claim 22 wherein the formulation further comprises a surfactant.
30. The method of claim 29 wherein the surfactant is selected from the group consisting of anionic, cationic, nonionic, zwitterionic and ampholytic surfactants.