Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractCompound Specific Stable Chlorine Isotopic Analysis of Volatile Aliphatic Compounds Using Gas Chromatography Hyphenated with Multiple Collector Inductively Coupled Plasma Mass Spectrometry    Next AbstractNMR assignment of the A form of the pheromone-binding protein of Bombyx mori »

Environ Sci Process Impacts


Title:"Isotope fractionation ((2)H/(1)H, (13)C/(12)C, (37)Cl/(35)Cl) in trichloromethane and trichloroethene caused by partitioning between gas phase and water"
Author(s):Horst A; Lacrampe-Couloume G;
Address:"Department of Isotope Biogeochemistry, Helmholtz Centre for Environmental Research - UFZ, Permoserstr. 15, 04318 Leipzig, Germany. axel.horst@ufz.de"
Journal Title:Environ Sci Process Impacts
Year:2020
Volume:20200129
Issue:3
Page Number:617 - 626
DOI: 10.1039/c9em00583h
ISSN/ISBN:2050-7895 (Electronic) 2050-7887 (Linking)
Abstract:"Transfer of organic compounds between aqueous and gaseous phases may change the isotopic composition which complicates the isotopic characterization of sources and transformation mechanisms in environmental samples. Studies investigating kinetic phase transfer of compounds dissolved in water (volatilization) are scarce, even though it presents an environmentally very relevant phase transfer scenario. In the current study, the occurrence of kinetic isotope fractionation ((2)H/(1)H, (13)C/(12)C, (37)Cl/(35)Cl) was investigated for two volatile organic compounds (trichloroethene, TCE and trichloromethane, TCM) during volatilization from water and gas-phase dissolution in water. In addition, experiments were also carried out at equilibrium conditions. The results indicated that volatilization of trichloromethane and trichloroethene from water, in contrast to pure phase evaporation, only caused small (chlorine) or negligible (hydrogen, carbon) isotope fractionation whereas for dissolution in water significant carbon isotope effects were found. At equilibrium conditions, hydrogen and carbon isotopes showed significant differences between dissolved and gaseous phase whereas small to insignificant differences were measured for chlorine isotopes. The results confirm the hypothesis that isotope effects during volatilization of organics from water are caused by transport inhibition in the aqueous phase. The consideration of gas-phase diffusion and vapor pressure isotope effects (Craig-Gordon model) could not reproduce the measured isotopic data. Overall, this study provides an overview of the most common kinetic and equilibrium partitioning scenarios and reports associated isotope effects. As such it illustrates under which environmental conditions isotopic signatures of chlorinated volatile organics may change, or remain constant, during transfer between surface waters and air"
Keywords:Carbon Isotopes Chemical Fractionation Chlorine Chloroform Gases *Trichloroethylene;
Notes:"MedlineHorst, Axel Lacrampe-Couloume, Georges eng England 2020/01/30 Environ Sci Process Impacts. 2020 Mar 1; 22(3):617-626. doi: 10.1039/c9em00583h. Epub 2020 Jan 29"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 19-12-2024