“…Fang and co-workers [ 50 ] exploited the layer-by-layer method for providing polyester fabrics with flame retardant and anti-drippring features. To this end, 1, 5, 10 and 20 bi-layers were deposited onto the synthetic fabric substrate.…”
Section: Chitosan and Its Derivatives As Flame Retardants For Textmentioning
confidence: 99%
“…( a ) uncoated polyester, ( b ) LbL-treated polyester—1 bi-layer, ( c ) LbL-treated polyester—5 bi-layers, ( d ) LbL-treated polyester—10 bi-layers and ( e ) LbL-treated polyester—20 bi-layers. Reprinted with permission from [ 50 ]. Copyright 2019, Elsevier.…”
During the last decade, the utilization of chitin, and in par0ticular its deacetylated form, i.e. chitosan, for flame retardant purposes, has represented quite a novel and interesting application, very far from the established uses of this bio-sourced material. In this context, chitosan is a carbon source that can be successfully exploited, often in combination with intumescent products, in order to provide different polymer systems (namely, bulky materials, fabrics and foams) with high flame retardant (FR) features. Besides, this specific use of chitosan in flame retardance is well suited to a green and sustainable approach. This review aims to summarize the recent advances concerning the utilization of chitosan as a key component in the design of efficient flame retardant systems for different polymeric materials.
“…Fang and co-workers [ 50 ] exploited the layer-by-layer method for providing polyester fabrics with flame retardant and anti-drippring features. To this end, 1, 5, 10 and 20 bi-layers were deposited onto the synthetic fabric substrate.…”
Section: Chitosan and Its Derivatives As Flame Retardants For Textmentioning
confidence: 99%
“…( a ) uncoated polyester, ( b ) LbL-treated polyester—1 bi-layer, ( c ) LbL-treated polyester—5 bi-layers, ( d ) LbL-treated polyester—10 bi-layers and ( e ) LbL-treated polyester—20 bi-layers. Reprinted with permission from [ 50 ]. Copyright 2019, Elsevier.…”
During the last decade, the utilization of chitin, and in par0ticular its deacetylated form, i.e. chitosan, for flame retardant purposes, has represented quite a novel and interesting application, very far from the established uses of this bio-sourced material. In this context, chitosan is a carbon source that can be successfully exploited, often in combination with intumescent products, in order to provide different polymer systems (namely, bulky materials, fabrics and foams) with high flame retardant (FR) features. Besides, this specific use of chitosan in flame retardance is well suited to a green and sustainable approach. This review aims to summarize the recent advances concerning the utilization of chitosan as a key component in the design of efficient flame retardant systems for different polymeric materials.
“…The more APP in the sample, the stronger this phenomenon is. 8,25,[36][37][38] In the analyzed case (Figure 3), the first peak appears at about 280 C and can be linked to the first decomposition step, that is, the release of ammonia, water and polyphosphoric acid, 19,25,[36][37][38] which then decomposes, reacting with resin at about 340 C. The formation of fire retardant charring starts at about 510 C and ends at 652 C (4% by weight of APP in the sample) and 714 C (8% by weight of APP in the sample), which significantly delays the total decomposition of epoxy resin.…”
Section: Intumescent Systemmentioning
confidence: 99%
“…The first, about −10 wt% (−20 wt% for control samples), is associated with two endothermic effects that are most likely the result of the initial decomposition of melamine, APP and pentaerythritol (Table 2). 1,14,17,19,25,[36][37][38][39][40][41][42][43][44] The effects associated with polymerization and crosslinking of epoxy resin are shifted by approximately 50 C towards higher temperatures. The peak at about 530 C associated with the complete decomposition of resin disappears only for the intumescent coatings (it is visible in the Figure 10), and instead of this, peaks at 736 C (A) and 630 C corresponding to the formation of a protective, intumescent and charred layer appear.…”
Section: Intumescent Coatingsmentioning
confidence: 99%
“…In this process, the P N bonds are stronger than the P O ones, thus keeping phosphorus in the condensed phase, resulting in a cross-linked structure that promotes a more intense formation of the charred protective layer, strengthen with the ceramic additives. 19,25,[36][37][38] 3.2 | Fire endurance tests analysis Figure 11 shows the dependence of the temperature increment on the surface of steel samples covered with Table 3 presents the results of the intumescent multiplication of analyzed coatings and time to reach the limit temperature. Control samples (A' and B') were not subjected to the fire endurance tests because during the preliminary tests (kept for 20 min at the temperature of 500 C) obtained protective layers were charred but did not expand (B') or charred layer collapsed (A') (results not attached here).…”
The article presents results of the research on the influence of graphite/kaolin and graphite/titanium oxide systems on thermal properties, intumescence degree and the integrity of the structure of intumescent protective films based on epoxy resins for steel. The TG/DTG/DSC analysis showed that graphite/kaolin system shifted the decomposition reaction of epoxy resin towards higher temperatures, even by about 30 C. Fire endurance tests and the SEM analysis confirmed these results because more thermally resistant (T 500 C reached after 37.5 min for 1.1 coating thickness), swollen (about 20 times) and homogeneous coatings were obtained. The presented results suggest that ceramic fire retardants can successfully cooperate with organic components in intumescent protective coatings for steel elements.
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