Read e-book online Agrochemical and pesticide desk reference PDF

By Michael A. Kamrin, John H. Montgomery

ISBN-10: 0849321794

ISBN-13: 9780849321795

Very good source books are mixed to shape a unmarried finished database that gives summaries of environmental properties

The Agrochemicals and insecticides table Reference on CD-ROM includes particular information regarding 137 insecticides, serving as a primer of environmental toxicology and an intensive exchange identify index. Profiles of every pesticide provide

  • regulatory information
  • toxicity assessments
  • environmental destiny data
  • physical properties
  • acceptable publicity restrict values

    This CD-ROM is an updated reference encouraged by way of the turning out to be variety of study courses and the continuing curiosity within the destiny, delivery, and remediation of damaging elements. Featured are environmental and physical/chemical info on greater than three hundred compounds, together with insecticides, herbicides, and fungicides.

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    Extra info for Agrochemical and pesticide desk reference

    Example text

    B. Walker, Eds. The Pesticide Manual — A World Compendium, 9th ed. (Great Britain: British Crop Protection Council, 1991), 1141 p. © 2000 CRC PRESS LLC ABBREVIATIONS AND SYMBOLS Å α αa αb ≈ ACGIH ASTM asym atm b B β BCF bp C °C cal CAS CEC CERCLA CHRIS cm CL CS DOT ds dw δ EC50 et al. 15) acid dissociation constant distribution coefficient (cm) base dissociation constant distribution coefficient (cm3/g) kilogram Henry’s law constant (atm · m3/mol · K) Henry’s law constant (dimensionless) soil/sediment partition coefficient (organic carbon basis) soil/sediment partition coefficient (organic matter basis) n-octanol/water partition coefficient kilohertz kilopascal dissociation constant for water (10–14 at 25°C) less than less than or equal to liter pound lethal concentration necessary to kill 50% of the aquatic species tested lethal concentration necessary to kill 100% of the aquatic species tested lethal dose necessary to kill 50% of the mammals tested lower explosive limit meter meta (as in m-dichlorobenzene) molarity (moles/liter) mass milliequivalents milligram minute(s) milliliter mass of sorbed solute millimeters of mercury millimole mole melting point mass of solute in solution millivolt normality (equivalents/liter) normal (as in n-propyl, N-nitroso) effective porosity nanogram National Institute for Occupational Safety and Health nanometer ortho (as in o-dichlorobenzene) Occupational Safety and Health Administration specific density (unitless) © 2000 CRC PRESS LLC pP Pa pair PEL pH pKa pKb pKw ppb ppm P-t1/2 pv QSAR R Ra Rb RCRA Rd Rf RTECS S Sa SARA secSo Sw sp.

    Photolytic. Major products reported from the photooxidation of formaldehyde with nitrogen oxides are carbon monoxide, carbon dioxide and hydrogen peroxide (Altshuller, 1983). , 1979). Calvert et al. (1972) reported, however, that formaldehyde photodecomposed by direct sunlight in the atmosphere yielding hydrogen, formyl radicals and carbon monoxide. Photooxidation of formaldehyde in the absence of nitrogen oxides in air (λ = 2900–3500 Å) gave hydrogen peroxide, alkylhydroperoxides, carbon monoxide and lower molecular weight aldehydes.

    Photolytic. Major products reported from the photooxidation of formaldehyde with nitrogen oxides are carbon monoxide, carbon dioxide and hydrogen peroxide (Altshuller, 1983). , 1979). Calvert et al. (1972) reported, however, that formaldehyde photodecomposed by direct sunlight in the atmosphere yielding hydrogen, formyl radicals and carbon monoxide. Photooxidation of formaldehyde in the absence of nitrogen oxides in air (λ = 2900–3500 Å) gave hydrogen peroxide, alkylhydroperoxides, carbon monoxide and lower molecular weight aldehydes.

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    Agrochemical and pesticide desk reference by Michael A. Kamrin, John H. Montgomery


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