2016
DOI: 10.1108/prt-11-2014-0103
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Preparation of waterborne P-N containing epoxy resin curing and its performances

Abstract: Purpose The flammability of epoxy resin is a major disadvantage in applications that require flame resistance. Epoxy monomers and hardeners containing flame-retardant elements are molecularly incorporated in the resin network are expected to exhibit better flame resistance than those borne on an additive approach. In recent years, because of health and environmental regulation, the use of waterborne coatings has received many attentions. However, waterborne epoxy resin curing agent with excellent flame retarda… Show more

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Cited by 9 publications
(4 citation statements)
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“…When the amount of acrylamide is small, the amount of -CONH 2 in the system is small, and the synergistic effect with -COONa increases the water absorption and salt resistance of the resin. When the amount of acrylamide is greater than a certain value, with the increase of acrylamide concentration, there are more and more -CONH 2 in the polymer, and the defect of insufficient hydrophilicity of -CONH 2 is obvious, which is not conducive to the water absorption of the polymer [58].…”
Section: Watermentioning
confidence: 99%
“…When the amount of acrylamide is small, the amount of -CONH 2 in the system is small, and the synergistic effect with -COONa increases the water absorption and salt resistance of the resin. When the amount of acrylamide is greater than a certain value, with the increase of acrylamide concentration, there are more and more -CONH 2 in the polymer, and the defect of insufficient hydrophilicity of -CONH 2 is obvious, which is not conducive to the water absorption of the polymer [58].…”
Section: Watermentioning
confidence: 99%
“…Water absorption was determined using the equation; (W bef -W aft )/W bef  100 per cent, where W bef and W aft are the weight of the cured film before and after immersion, respectively. The cured films were immersed in deionized water for 24 h (Li et al, 2016).…”
Section: Characterizationmentioning
confidence: 99%
“…This is because when the resins were combusted in air, the P element in the resin was decomposed and generated the phosphoric acid or polyphosphoric acid which promoted the char yield, and therefore formed a compact char residue structure (Sergei et al, 2005). This compact carbon char structure can resist both mass and heat transfer and act as barriers to segregate the transportation of heat, combustible gas and oxygen, therefore reducing the smoke production, heat release and mass loss (Li et al, 2016). However, from Figures 4 (c) and (f), it can be seen that the interior char residue of the P-N containing resin system showed more porous and loose structure compared to the Pcontaining resin system that still displayed a rather compact structure.…”
Section: Micro-morphology Of the Char Residuementioning
confidence: 99%
“…The system was raised to 70 °C, and 26.0 g (0.2 mol) of BGE was added. The reaction was continued for another 3 h to form product II (Li 2016). The solution was cooled to 50 °C and neutralized by various amounts of acetic acid to obtain a self-emulsified epoxy curing agent with various neutralization degrees.…”
Section: Preparation Of Self-emulsified Epoxy Curing Agentmentioning
confidence: 99%