2022
DOI: 10.1016/j.polymdegradstab.2021.109799
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Universal circulating impregnation method for the fabrication of durable flame-retardant plywood with low hygroscopicity and leaching resistance

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Cited by 14 publications
(4 citation statements)
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“…When comparing the peak heat release rate with those described in other literature on flame-retardant plywood [43][44][45][46][47], the results indicate that the majority of adhesives used in the literature were formaldehyde-based, which are not environmentally friendly. As depicted in Figure 6, the UCPR-LDH plywood developed in this study not only exhibits superior thermal barrier performance but also ensures formaldehyde-free emissions while being flame-retardant.…”
Section: Cone Calorimetrymentioning
confidence: 85%
“…When comparing the peak heat release rate with those described in other literature on flame-retardant plywood [43][44][45][46][47], the results indicate that the majority of adhesives used in the literature were formaldehyde-based, which are not environmentally friendly. As depicted in Figure 6, the UCPR-LDH plywood developed in this study not only exhibits superior thermal barrier performance but also ensures formaldehyde-free emissions while being flame-retardant.…”
Section: Cone Calorimetrymentioning
confidence: 85%
“…In addition, boron compounds were also applied in preparing fire-retardant plywood [9,10]. Though these nitrogen, phosphorus, and boron-based compounds had the disadvantages of hygroscopicity and poor water resistance, which could leach out [11][12][13] and damage the bonding strength of the plywood [14,15], the excellent fireproof properties of these fire retardants still make them the most commonly used flame retardants for plywood by impregnating modification.…”
Section: Introductionmentioning
confidence: 99%
“…The mode of action of such intumescent VAE polymer was initiated by the emission of polyphosphoric acids at the temperature around 200°C, 15–17 and the VAE chains started to decompose until being heated exceeding 240°C, 18–20 thus, the intumescent additive inside typically began to degrade earlier than decomposition of the VAE matrix. The polyphosphoric acids emitted then reacted with the phenolic hydroxyl groups in sodium lignosulfonate (SL) to form a phosphor‐carbonaceous layer at the exterior through dehydrating 21,22 . After forming such phosphorus‐carbonaceous layer, main low‐flammability gasses (i.e., CO 2 and NH 3 ) were released owing to the decomposition of MEL amino trimethyl phosphate (M‐AT) at the temperature around 330°C, 23–25 as a result, the char layer began to expand, a stable, bubble‐shaped and low‐thermal‐conductivity phosphorus‐carbonaceous layer on the surface of VAE polymer was finally created 26 .…”
Section: Introductionmentioning
confidence: 99%
“…The polyphosphoric acids emitted then reacted with the phenolic hydroxyl groups in sodium lignosulfonate (SL) to form a phosphor-carbonaceous layer at the exterior through dehydrating. 21,22 After forming such phosphorus-carbonaceous layer, main low-flammability gasses (i.e., CO 2 and NH 3 ) were released owing to the decomposition of MEL amino trimethyl phosphate (M-AT) at the temperature around 330 C, [23][24][25] as a result, the char layer began to expand, a stable, bubble-shaped and lowthermal-conductivity phosphorus-carbonaceous layer on the surface of VAE polymer was finally created. 26 Consequently, an imperative investigation pertained to the optimal mass ratio of M-AT to sodium lignosulfonate (SL) within intumescent VAE polymers.…”
Section: Introductionmentioning
confidence: 99%