1997
DOI: 10.1021/jf960487o
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Controlled Release of 2,4-D from Granule Matrix Formulations Based on Six Lignins

Abstract: Six lignins were used to obtain granular controlled release matrix formulations of the herbicide 2,4-D (2,4-dichlorophenoxyacetic acid). The water insoluble lignins were sourced from sugar cane (Saccharum officinarum) bagasse and Eucalyptus sp. and Pinus sp. woods. Each lignin was characterized by its functional groups and molecular weight distributions. The formulations were prepared by melting the 2,4-D and mixing in the lignins individually and then granulating (to 0.7−1.0 mm) the glassy matrix. Release ra… Show more

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Cited by 39 publications
(29 citation statements)
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References 5 publications
(1 reference statement)
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“…A few approaches were taken to prepare controlled release formulations: formulations based on alginate (9), cyclodextrin complexes (10), formulations based on lignin (11), polymer encapsulation (12), formulations based on starch (13), and formulations based on organo-clays (14,15). These formulations were designed for hydrophobic herbicides.…”
Section: Introductionmentioning
confidence: 99%
“…A few approaches were taken to prepare controlled release formulations: formulations based on alginate (9), cyclodextrin complexes (10), formulations based on lignin (11), polymer encapsulation (12), formulations based on starch (13), and formulations based on organo-clays (14,15). These formulations were designed for hydrophobic herbicides.…”
Section: Introductionmentioning
confidence: 99%
“…Several approaches have been employed to obtain CRFs: alginate encapsulation (Gerstl et al, 1998), cyclodextrin complexation (Loukas et al, 1994), polymeric microcapsules (Dailey et al, 1993), lignin entrapment (Ferraz et al, 1997), and starch encapsulation (Mervosh et al, 1995). This latter was essayed for norflurazon (Boydston, 1992).…”
Section: Introductionmentioning
confidence: 99%
“…DFRC was performed as described by Lu and Ralph (25,26). 4-Acetoxy-3-methoxycinnamyl acetates (DFRC monomers, both cis and trans isomers) were separated by gas chromatography-mass spectrometry (GC-MS) and identified based on their mass spectra, which were identical to those from authentic compounds, including coniferyl diacetate (m/z [relative intensity] ϭ 264 [9], 222 [100], 179 [50], 163 [11], 151 [14], 131 [20], 119 [12], 91 [9]). The amounts of each monomer were determined by GC and flame ionization detection by using a response factor (1.40) derived from pure monomer standards, with 4,4Ј-ethylene bisphenol as the internal standard.…”
mentioning
confidence: 99%
“…Fourier transform infrared (FTIR) spectra were obtained with a Nicolet 520 FTIR spectrophotometer and a KBr disk containing 0.5% of the sample. The elemental analysis and methoxyl contents were determined by following methods previously described (11). 1 H, 13 C, distortionless enhancement by polarization transfer with a of 135°( DEPT-135), and heteronuclear multiple quantum coherence (HMQC) spectra were obtained with a Bruker DRX-360 instrument.…”
mentioning
confidence: 99%