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Tytuł artykułu

Synthesis and evaluation of effectiveness of a controlled release preparation 2,4-D: a reduction of risk of pollution and exposure of workers

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A novel herbicidal controlled release formulation composed of (2,4-dichlorophenoxy) acetic acid (2,4-D) chemically bonded to biodegradable (R,S)-3-hydroxybutyric acid oligomers was investigated. The synthesis of (R,S)-3-hydroxy butyric acid oligomers was carried out via the ring opening polymerization of â-butyrolactone initiated by 2,4-dichlorophenoxy acetic potassium salt in the presence of complexing agents. The formed oligomers were characterized by size exclusion chromatography, proton magnetic resonance and electrospray mass spectrometry in order to fi nd out their molar mass distribution and molecular structures. An assessment of biological effectiveness of the obtained herbicidal formulation was carried out in the greenhouse vs. Sinapis alba var. Nakielska. A promotion of the controlled release formulation with decreased water solubility and with low vapor pressure of the active ingredient, instead of traditional formulations of 2,4-dichlorophenoxy acetic acid may help to ensure a greater safety for workers and reduce the risk of dissemination of the active ingredient in the soil profile.
Rocznik
Strony
119--129
Opis fizyczny
Bibliogr. 15 poz., tab., wykr.
Twórcy
autor
autor
  • Institute of Chemistry, Environmental Protection and Biotechnology Jan Długosz University, Częstochowa PL-42-200, wjk@interia.pl
Bibliografia
  • [1] Akelah A.: Novel utilizations of conventional agrochemicals by controlled release formulations, Mater. Sci. Eng. C 4, 83 (1996).
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  • [3] Bahadi M.: Safe formulations of agrochemicals, Chemosphere, 16, 615 (1987).
  • [4] Bhattacharya S., Sanya S.K., Mukherje R.N.: Controlled-Release Polymeric Herbicide Formulations with Pendent 2,4-Dichlorophenoxyacetic Acids, Ind. Eng. Chem. Prod. Res. Dev. 25, 585 (1986).
  • [5] Buser H.R., Mueller M.D.: Occurrence and transformation reactions of chiral and achiral phenoxyalkanoicacid herbicides in lakes and rivers in Switzerland, Environ. Sci. Technol., 32, 626 (1998).
  • [6] Celis R., Koskinen W.C., Cecchi A.M., Bresnahan G.A., Carrisoza M.J., Ulibarri M.A., Pavlovic I., Hermosin M.C.: Sorption of the ionizable pesticide imazamox by organo-clays and organohydrotalcites, J. Environmental Science & Health, Part B: Pesticides, Food Contaminants, and Agricultural Wastes, 34 (6), 929 (1999).
  • [7] Cottefi ll J.V., Wilkins R.M., da Silva F.T.: Controlled release of diuron from granules based on a ligninmatrix system, J. Controlled Release, 40, 133 (1996).
  • [8] Curwin B.D., Hein M.J., Sanderson W.T., Nishioka M.G., Reynolds S.J., Ward E.M., Alavanja M.C.: Pesticide Contamination Inside Farm and Nonfarm Homes, J. Occupational & Environmental Hygiene, 2 (7), 357 (2005).
  • [9] Elbahri Z., Taverdet J.-L.: Elaboration of microspheres and coated microspheres for the controlled release of the herbicide 2,4-D, Polymer Bulletin, 59, 709 (2007).
  • [10] Focarete M.L., Scandola M., Jendrossek D., Adamus G., Sikorska W., Kowalczuk M.: Bioassimilation of Atactic Poly[(R,S)-3-hydroxybutyrate Oligomers by Selected Bacterial Strains, Macromolecules, 32 (15), 4814.
  • [11] Garrido-Herrera F.J., Daza-Fernández I., González-Pradas E., Fernández-Pérez M.:Lignin-based formulations to prevent pesticides pollution, J. Hazard. Mater., 168, 220 (2009).
  • [12] Hyun S., Lee L.S.: Quantifying the contribution of different sorption mechanisms for 2,4-dichlorophenoxyaceticacid sorption by several variable-charge soils, Environ. Sci. Technol., 39, 2522 (2005).
  • [13] Knowles A.: Recent developments of safer formulations of agrochemicals, Environmentalist., 28, 35 (2008).
  • [14] Kulkarni A.R., Soppimatha K.S., Aminabhavi T.M., Dave A.M., Mehta M.H.: Glutaraldehyde crosslinkedsodium alginate beads containing liquid pesticide for soil application, J. Controlled Release, 63, 97 (2000).
  • [15] Kurcok P., Kowalczuk M., Hennek K., Jedlinski Z.: Anionic polymerization of β-lactones initiated withalkali-metal alkoxides: reinvestigation of the polymerization mechanism, Macromolecules., 25 (7), 1992.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUS8-0024-0011
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