2011
DOI: 10.1134/s1070427211090278
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Preparation of modified hydrolysis lignin and its use for filling epoxy polymers and enhancing their flame resistance

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Cited by 25 publications
(14 citation statements)
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“…Moreover, its aromatic chemical leads to a high char yield after decomposition (around 40% at 900°C). 31 Various lignins (raw and chemically modified) were recently incorporated in various flame retardant systems for biobased polymers and biobased composites, [32][33][34][35] In the present study, combinations of nanoclays, lignin and APP at micronic scale, will be proposed to try to combine the interest of the formation of metallic phosphates and charring activity on PBS fire retardancy. New developments aiming to use lignin at nanometric scale in flame retardant systems are also in progress and will be detailed in a next article.…”
Section: Marney Et Almentioning
confidence: 99%
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“…Moreover, its aromatic chemical leads to a high char yield after decomposition (around 40% at 900°C). 31 Various lignins (raw and chemically modified) were recently incorporated in various flame retardant systems for biobased polymers and biobased composites, [32][33][34][35] In the present study, combinations of nanoclays, lignin and APP at micronic scale, will be proposed to try to combine the interest of the formation of metallic phosphates and charring activity on PBS fire retardancy. New developments aiming to use lignin at nanometric scale in flame retardant systems are also in progress and will be detailed in a next article.…”
Section: Marney Et Almentioning
confidence: 99%
“…Moreover, its aromatic chemical leads to a high char yield after decomposition (around 40% at 900°C) . Various lignins (raw and chemically modified) were recently incorporated in various flame retardant systems for biobased polymers and biobased composites, including PBS since the pioneering work of De Chirico et al who incorporated lignin with APP in PP. Owing to the nature of the chemical groups linked to their aromatic structures, lignins can be dehydrated by polyacids such as APP and hence can be integrated in intumescent flame retardant systems.…”
Section: Introductionmentioning
confidence: 99%
“…The amount of hydroxyl groups in the initial THL was established from the data given in [4] (Table 1). Reactivity of OH-groups in THL depends not only on their amount in the initial sample but also on spatial organization of the THL macromolecule.…”
Section: Resultsmentioning
confidence: 99%
“…Lignin phosphorylation has been carried out under different conditions using various phosphorus reagents, such as phosphorus trihalides, phosphorus oxyhalides, phosphorus thiohalides, phosphorus oxides, and phosphorus sulfides, for instance. [44][45][46][47] Tetrahydrofuran, 38,48 pyridine, 39,49 acetonitrile, 47 dimethylformamide, formaldehyde 44,45 and urea 37 were also used as solvents for phosphorylation in different studies. The reaction conditions were reported to occur in the time range of 1-12 h and the temperature range of 25-180°C.…”
Section: Introductionmentioning
confidence: 99%
“…38,47,49,50 The phosphorylated group on lignin has facilitated its use as a high-performance flame-retardant additive in polyurethane, polybutylene succinate, polypropylene, epoxy and polylactic acid. 39,[44][45][46][47] The proposed application is attributed to the fact that the phosphorylation of aromatic compounds Fig. 1 General S N 2 reaction mechanism between lignin and substrate to form a new product and a leaving group (L).…”
Section: Introductionmentioning
confidence: 99%