2006
DOI: 10.1021/jf0614488
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Competitive Sorption−Desorption Behavior of Triazine Herbicides with Plant Cuticular Fractions

Abstract: Sorption interactions of plant cuticular matter with organic compounds are not yet fully understood. The objective of this study was to examine the competitive sorption-desorption interactions of the triazine herbicides (atrazine and ametryn) with cuticular fractions isolated from tomato fruits and leaves of Agave americana. The 13C NMR data suggest a rubber-like nature for the cutin. This biopolymer exhibited reversible and noncompetitive sorption. Enhanced desorption of atrazine was recorded in the bi-solute… Show more

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Cited by 29 publications
(34 citation statements)
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“…Cutin biodegradation has been observed by Kögel-Knabner et al (1989) andStimler et al (2006). Though this process (depolymerization) does not significantly affect the amount of organic matter, the sorption capability of the system is drastically decreased due to the high sorptive capacity of the cutin (Chamel and Vitton 1996;Chefetz 2003;Chen et al 2005;Shechter et al 2006).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Cutin biodegradation has been observed by Kögel-Knabner et al (1989) andStimler et al (2006). Though this process (depolymerization) does not significantly affect the amount of organic matter, the sorption capability of the system is drastically decreased due to the high sorptive capacity of the cutin (Chamel and Vitton 1996;Chefetz 2003;Chen et al 2005;Shechter et al 2006).…”
Section: Resultsmentioning
confidence: 99%
“…In addition to the importance of plant cuticular matter as possible precursors for SOM, these and other natural aliphatic-rich materials have been recently reported as highly efficient natural sorbents for hydrophobic and polar organic compounds (Boyd et al 1990;Chefetz 2003;Chefetz et al 2000;Chen et al 2005;Kang and Xing 2005;Salloum et al 2002;Shechter et al 2006;Stimler et al 2006). In most cases, sorption of hydrophobic organic compounds (HOCs) by these sorbents, including plant cuticular materials, is in the same range or even higher than the sorption affinity values reported for aromatic-rich natural sorbents.…”
mentioning
confidence: 99%
“…Th e peak at 17.5 ppm can be assigned to terminal methyl groups (Swift , 1996), suggesting that SM-HA has more terminal methyl C than the other HAs and potentially greater reactivity. Th e sharp peak at around 31 ppm found in all the HAs represents carbons in long crystalline or condensed polymethylenic (CH 2 ) n chains (Kögel-Knabner et al, 1992;Shechter et al, 2006). Th is peak is more evident in SM-HA than in FM-HA and FS-HA, respectively.…”
Section: Cross-polarization Magic Angle Spinning Carbon-13 Nuclear Mamentioning
confidence: 95%
“…In the literature there are some examples of cutin extraction methods combining organic solvent extraction and acid hydrolysis [255,256]. In some cases, an additional pretreatment of tomato skins is performed, which consists of a heat treatment with oxalic acid and ammonium oxalate to remove the residual pulp, that can remain attached to the skins [257].…”
Section: Cutin Extraction From Tomato Skinsmentioning
confidence: 99%