2006
DOI: 10.1016/j.jpcs.2006.01.076
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Intercalation and controlled release of 2,4-dichlorophenoxyacetic acid using rhombohedral [LiAl2(OH)6]Cl·xH2O

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Cited by 22 publications
(10 citation statements)
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“…The release profile obtained in this study, i.e., a high burst followed by a slow release, is similar to those previously reported in the literature that used 2,4-D as adsorbate and clay materials as adsorbents (layered double hydroxides (LDH), also called anionic clays, and others organically modified clay, for instance [53][54][55]), that were aimed to be applied as herbicide controlled release formulations. Despite the similarity, the release studies performed by Ragavan et al [53], Bashi et al [54], and Hermosín et al [55] reached equilibrium in approximately 100-1440 min (1 day), while in this work the equilibrium was not reached in the time range studied. According to the release models applied to our data (Weibull, Logistic and Makoid-Banakar), shown in Fig.…”
Section: Release Studysupporting
confidence: 86%
“…The release profile obtained in this study, i.e., a high burst followed by a slow release, is similar to those previously reported in the literature that used 2,4-D as adsorbate and clay materials as adsorbents (layered double hydroxides (LDH), also called anionic clays, and others organically modified clay, for instance [53][54][55]), that were aimed to be applied as herbicide controlled release formulations. Despite the similarity, the release studies performed by Ragavan et al [53], Bashi et al [54], and Hermosín et al [55] reached equilibrium in approximately 100-1440 min (1 day), while in this work the equilibrium was not reached in the time range studied. According to the release models applied to our data (Weibull, Logistic and Makoid-Banakar), shown in Fig.…”
Section: Release Studysupporting
confidence: 86%
“…The insertion of 2,4-D occurred in the interlayer, resulting in the expansion of basal spacing from 8.9 to 20.1 Å. Previous study on the intercalation of 2,4-D into various LDH systems showed slightly different d -spacing, as the value reported is very much depending on the parameters used for the synthesis [9,31-34]. The increase in basal spacing indicated that the interlayer has been expanded in order to accommodate the 2,4-D moiety, which is bigger in size compared to the nitrate as the counter anion in the LDH.…”
Section: Resultsmentioning
confidence: 99%
“…FTIR spectra for cloprop showed a broad band at 2959 cm −1 which is attributed to the O-H stretching vibration. A sharp band at 1715 cm −1 is due to the stretching of C = O and bands at 1465 and 1404 cm −1 are attributed to stretching vibrations of aromatic ring C = C. A strong band at 1277 and 1215 cm −1 were due to the symmetric and asymmetric stretching modes of C-O-C of the cloprop anions while a sharp band at 746 cm −1 is due to C-Cl stretching band of both anions [15]. The FTIR spectrum of cloprop-LDH and cloprop-ZLH synthesized using 0.2 M cloprop are also shown in Figure 2. As expected, the spectrum resembles a mixture of both FTIR spectra of cloprop and Zn/Al-LDH, indicating that both functional groups of cloprop and Zn/Al-LDH are present together, except for the peak at 1389 cm −1 and 1713 cm −1 corresponding to the nitrate anions and carboxylic group.…”
Section: Ftirmentioning
confidence: 97%