Claims
- 1. A dispersion of a pesticidally effective amount of solid, dry particles of a thiocarbonate selected from the group consisting of thioesters, and complexes of thiocarbonates and salts, said salts selected from the group consisting of ammonium, alkali metal, and alkaline earth metal tri- and tetrathiocarbonates, and combinations thereof, in a water resistant, biodegradable wax.
- 2. The composition defined in claim 1, wherein said thiocarbonate is of the form:
- M.sub.c (C.sub.a S.sub.b).sub.y
- wherein M is hydrogen, a cationic salt forming moiety or the organic moiety of a mercaptan, a ranges between 1 and about 4, b ranges between about 3 and about 9, c is the valence of (C.sub.a S.sub.b) and y is the valence of M.
- 3. The composition defined in claim 2, wherein a ranges between 1 and 3, b ranges between 3 and 5, and c is 1 or 2.
- 4. The composition of claim 2, wherein a is 1, b is 3 or 4 and c is 2.
- 5. The composition of claim 4, wherein M is a cationic salt-forming moiety selected from the group consisting of ammonium, quaternary ammonium, quaternary phosphonium, quaternary arsonium, metals and metal complexes formed with ammonia, ethylenediamine, diethylenetriamine, propylenediamine and pyridine.
- 6. The composition of claim 2, wherein M is an organic radical selected from the group consisting of alkyl, cycloalkyl, aryl, alkylaryl and arylalkyl groups.
- 7. The composition of claim 2, wherein M is an alkyl group having form 1 to about 8 carbon atoms.
- 8. The composition defined in claim 1, wherein said thiocarbonate is a complex having as a ligand thereof a group of the form:
- (C.sub.a S.sub.b)
- wherein a ranges between 1 and about 4, and b ranges between about 3 and about 9.
- 9. The composition of claim 1, wherein said thiocarbonate comprises the product of the process comprising:
- reacting carbon disulfide and a source of sulfide of the form M.sub.2 S.sub.y, wherein M is a cationic salt-forming moiety, and y is the valence of M, said reaction being performed in a liquid water-free medium under conditions sufficient to produce a trithiocarbonate salt of the general form M.sub.2 (CS.sub.3).sub.y.
- 10. The composition of claim 9, wherein said cationic salt-forming moiety is ammonium or an alkali metal.
- 11. The composition of claim 9, wherein said liquid water-free medium is selected from the group consisting of methanol, ethanol, propanol, isopropanol, n-butanol, isobutanol and secondary butanol.
- 12. The composition of claim 9, wherein the sources of sulfide and carbon disulfide are present in a stoichiometric mixture for the general reaction:
- M.sub.2 S.sub.y +y CS.sub.2 .fwdarw.M.sub.2 (CS.sub.3).sub.y.
- 13. The composition of claim 9, wherein said water-free medium is methanol and/or ethanol and, after said thiocarbonate salt is formed, said reaction further comprises the steps of dissolving an alcohol soluble salt of a heavy metal selected from the group consisting of iron, copper, nickel, zinc, lead and cadmium in said medium and reacting same with said thiocarbonate salt.
- 14. The composition of claim 9, wherein said source of sulfide is produced by the steps of:
- a) reacting an alkali metal hydroxide with a water-free alcohol selected from the group consisting of methanol, ethanol, propanol, isopropanol, n-butanol, isobutanol and secondary butanol, to form a solution of water and an alkoxide of the form, MOA, wherein M is an alkali metal radical and A is an alkyl group;
- b) removing said water from said alcohol solution;
- c) reacting said alkoxide with hydrogen sulfide to form said source of sulfide.
- 15. The composition defined in claim 1, wherein said wax comprises paraffin wax.
CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a continuation-in-part of patent application Ser. No. 290,992, filed Dec. 29, 1988, now U.S. Pat. No. 5,039,327, which itself is a continuation-in-part of both Ser. No. 253,139, filed Oct. 4, 1988, now U.S. Pat. No. 4,908,143, and Ser. No. 260,912 filed Oct. 21, 1988, now U.S. Pat. No. 4,908,142.
US Referenced Citations (20)
Foreign Referenced Citations (1)
Number |
Date |
Country |
892450 |
Mar 1962 |
GBX |
Non-Patent Literature Citations (4)
Entry |
Journal of the Chemical Society, vol. 89 (II), pp. 1812-1818 (1906), O'Donoghue and Kahan. |
Journal of the Chemical Society, vol. 119, pp. 38-54 (1921), Yeoman. |
Journal of the Chemical Society, vol. 128 (II), pp. 2326-2332 (1928), Mills and Robinson. |
"Carbon Sulfides and Their Inorganic and Complex Chemistry," Gattow and Behrendt, Topics in Sulfur Chemistry, A. Senning, Editor, George Thieme Publishers, Stuttgart, pp. 173-177, (1977). |
Continuation in Parts (2)
|
Number |
Date |
Country |
Parent |
290992 |
Dec 1988 |
|
Parent |
253139 |
Oct 1988 |
|