Incompatibility of metam sodium with halogenated fumigants

Mingxin Guo1, Scott R Yates, Sharon K Papiernik

  • 1Department of Environmental Sciences, University of California, Riverside, CA 92521, USA. mingxin.guo@ucr.edu

Insights

Metam sodium (metam) is incompatible with halogenated fumigants, causing their rapid degradation. Simultaneous soil application reduces pest control efficacy, recommending sequential or depth-separated treatments for combined use.

Area of Science:

  • Agricultural Chemistry
  • Soil Science
  • Pest Management

Background:

  • Metam sodium (metam) is a common soil fumigant used for broad-spectrum pest control.
  • Combined application with other fumigants aims for synergistic pesticidal effects.
  • Compatibility of metam with halogenated fumigants is crucial for effective soil fumigation strategies.

Purpose of the Study:

  • To evaluate the chemical compatibility of metam sodium with several halogenated fumigants.
  • To determine the degradation rates of halogenated fumigants when mixed with metam sodium.
  • To assess the impact of simultaneous application on pest control efficacy in soil.

Main Methods:

  • Metam sodium and halogenated fumigants (1,3-dichloropropene, chloropicrin, methyl bromide, methyl iodide, propargyl bromide) were simultaneously introduced into organic solvents, water, and moist soils.
  • Metam-induced degradation of halogenated fumigants was quantified using chemical analysis.
  • Field application simulations using Telone C-35 and Vapam in soil were conducted to assess degradation and efficacy.

Main Results:

  • Halogenated fumigants rapidly degraded when mixed with metam sodium in all tested media (solvents, water, soil).
  • Degradation rates increased with higher concentrations of metam sodium and varied by fumigant species.
  • In soil, metam sodium decomposed 15-95% of halogenated fumigants within 72 hours at a 1:1 molar ratio.
  • Simultaneous application of Telone C-35 and Vapam led to complete chloropicrin disappearance and partial 1,3-D degradation within 8 hours.

Conclusions:

  • Metam sodium is chemically incompatible with halogenated fumigants, leading to significant degradation.
  • Simultaneous application at the same soil depth is unlikely to maximize pest control due to fumigant inactivation.
  • Sequential application or application at different soil depths is recommended for effective combined use of metam sodium and halogenated fumigants.

Related Concept Videos

Amines to Sulfonamides: The Hinsberg Test01:23

Amines to Sulfonamides: The Hinsberg Test

The Hinsberg test is a method to identify primary, secondary and tertiary amines, named after its pioneer, Oscar Hinsberg. Here, amines are treated with benzenesulfonyl chloride, also known as the Hinsberg reagent, in the presence of an excess of aqueous base, followed by acidification. Based on the nature of the amines, different changes are observed.
Generally, a primary amine reacts with the Hinsberg reagent to produce an N-substituted benzenesulfonamide. The electron-withdrawing sulfonyl...
Halogens03:01

Halogens

Group 17 elements, known as halogens, are nonmetals. At room temperature, fluorine and chlorine are gases, bromine is a liquid, and iodine a solid. Astatine is a highly unstable radioactive element, so currently, most of its properties are unknown due to its short half-life. Tennessine is a synthetic element also predicted to be in this group.
ortho–para-Directing Deactivators: Halogens01:24

orthopara-Directing Deactivators: Halogens

Halogens are ortho–para directors. They are more electronegative than carbon. Therefore, as ring substituents, they can withdraw electrons through the inductive effect and deactivate the aromatic ring towards electrophilic substitution. Halogens also have an electron-donating resonance effect on the ring, which influences the orientation of the incoming electrophile. If an electrophile attacks at the ortho or the para position, the halogen donates electrons and stabilizes the intermediate...
Preparation and Reactions of Sulfides02:26

Preparation and Reactions of Sulfides

Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
Precipitation Reactions03:10

Precipitation Reactions

In a precipitation reaction, aqueous solutions of soluble salts react to give an insoluble ionic compound – the precipitate. The reaction occurs when oppositely charged ions in solution overcome their attraction for water and bind to each other, forming a precipitate that separates out from the solution. Since such reactions involve the exchange of ions between ionic compounds in aqueous solution, they are also referred to as double displacement, double replacement, exchange reactions, or...
Diazonium Group Substitution: –OH and –H01:19

Diazonium Group Substitution: –OH and –H

Nitrous acid, a weak acid, is prepared in situ via the reaction of sodium nitrite with a strong acid under cold conditions. This nitrous acid prepared in situ reacts with primary arylamines to form arenediazonium salts. Such reactions are known as diazotization reactions. As shown in Figure 1, the formation of arenediazonium salts begins with the decomposition of nitrous acid in an acidic solution to give nitrosonium ions.