Abstract:In order to improve the performance of phenolic foam, an additive compound of 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) and Itaconic acid (ITA) were attached on the backbone of ethyl cellulose (EC) and obtained DOPO-ITA modified EC (DIMEC), which was used to modify phenolic resin and composite phenolic foams (CPFs). The structures of DOPO-ITA were verified by Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (1H NMR). The molecular structure and microstructure were … Show more
“…The specific strength [ 1 , 2 , 3 , 4 , 5 ] and dimensional stability of foaming materials [ 6 ] are directly related to cell density, which is determined by the number of cells present during the foaming process. Therefore, the quality of foaming materials can be effectively improved by regulating nucleation in the foaming process [ 7 , 8 , 9 , 10 , 11 , 12 ].…”
Three types of organic cage compounds, namely, cucurbit[6]uril (Q[6]), hemicucurbit[6]uril (HQ[6]), and β-cyclodextrin (BC), with different cavity structures as heterogeneous nucleation agents were selected for a polypropylene (PP) foaming injection molding process. The experimental results showed that Q[6] with a “natural” cavity structure possessed the best nucleation efficiency of these three cage compounds. The nucleation mechanism of organic cage compounds was explored through classical nucleation theory, molecular structure, and in situ visual injection molding analysis.
“…The specific strength [ 1 , 2 , 3 , 4 , 5 ] and dimensional stability of foaming materials [ 6 ] are directly related to cell density, which is determined by the number of cells present during the foaming process. Therefore, the quality of foaming materials can be effectively improved by regulating nucleation in the foaming process [ 7 , 8 , 9 , 10 , 11 , 12 ].…”
Three types of organic cage compounds, namely, cucurbit[6]uril (Q[6]), hemicucurbit[6]uril (HQ[6]), and β-cyclodextrin (BC), with different cavity structures as heterogeneous nucleation agents were selected for a polypropylene (PP) foaming injection molding process. The experimental results showed that Q[6] with a “natural” cavity structure possessed the best nucleation efficiency of these three cage compounds. The nucleation mechanism of organic cage compounds was explored through classical nucleation theory, molecular structure, and in situ visual injection molding analysis.
“…Carvalh, G. et al [18], Li, J.; Wang, W. et al [19], Li, J. and Zhang, J. et al [20] all used a lignin moiety to replace the phenol with formaldehyde to form a phenolic resin to increase its viscosity, reduce formaldehyde emissions, and increase the strength of the phenolic foam. Ma, Y. et al introduced DOPO-ITA into the phenolic resin to improve the residual carbon and the cell distribution [21]. Turunen, M. et al used starch, urea and lignin as the phenolic resin modifiers to change the methylene bridge content of the resin by changing the molar mass ratio [22].…”
In this present study, 3-pentadecyl-phenol was selected as a modifier to prepare a foamable phenolic resin with excellent performance, which was successfully prepared by in situ modification. Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (1H NMR, 13C NMR) were used to test and characterize the molecular structure of the modified resin. The results showed that 3-pentadecyl-phenol successfully modified the molecular structure of phenolic resin with a reduction in the resin gel time. The effect of changing the added amount of 3-pentadecyl-phenol on the mechanical properties, microstructure, and flame retardancy of the modified foam was investigated. The results showed that when the amount of added 3-pentadecyl-phenol was 15% of the total amount of phenol, this resulted in the best toughness of the modified foam, which could be increased to 300% compared to the bending deflection of the unmodified phenolic foam. The cell structure showed that the modified phenolic foam formed a more regular and dense network structure and the closed cell ratio was high. Furthermore, the compressive strength, bending strength, and limited oxygen index were improved, while the water absorption rate was lowered. However, the foam density could be kept below 40 mg/cm3, which does not affect the load.
“…10), the toughness of DCMPFs was fail. Therefore, the ratio of mass was increased [30]. The results showed that the content of DOPO-g-CNSL/P was not too much, the better dosage of DOPO-g-CNSL/P was no more than 10%.…”
Section: Fragility Of Dcmpfsmentioning
confidence: 97%
“…4. For DOPO, the signal around 6.56 to 8.86 ppm was corresponded to the phenyl protons [28][29][30][31]. For CNSL, the chemical shifts of H a , H b , H c , H d and H e were observed at 0.97 ppm, 1.38 ppm, 2.10 ppm, 1.64 ppm and 2.60 ppm respectively, and the signal around 5.44 ppm (H f ) was corresponded to double bonds protons [10].…”
In order to improve the mechanical properties without reducing its flame retardancy of phenolic foams (PFs), 9, 10-dihydro-9-oxa-10phosphaphenanthrene-10-oxide (DOPO) was introduced in the structure of cashew nut shell liquid (CNSL) to improve its flame retardant, and the product of DOPO grafting CNSL (DOPO-g-CNSL) was obtained to modify phenolic resin, and to prepare DOPO-g-CNSL modified PFs (DCMPFs). The structures of DOPO-g-CNSL were verified by Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (1 H-NMR). Compared with CNSL, thermal stability of DOPO-g-CNSL was decreased and Ti decreased by 3.53%, but the residual carbon (800°C) was increased by 35.05%. Compared with pure PF, the mechanical properties, toughness and flame retardancy of DCMPFs were increased when the ratio of DOPO-g-CNSL to phenol (DOPO-g-CNSL/P) was no more than 10%. With the dosage of DOPO-g-CNSL/P increased, Ti of DCMPFs was slightly increased, but the carbon residues (800°C) were almost unchanged. And the cell sizes of DCMPFs were basically the same as the pure PF. By comprehensive analysis, the suitable dosage of DOPO-g-CNSL/P was no more than 10%.
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