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. 2020 Jul 29;12(8):1701. doi: 10.3390/polym12081701

Table 2.

Flame retardant PP materials containing nitrogen-based (N) flame retardants. Data are extracted from the literature: cone calorimetry parameters (TTI, pHRR, THR), LOI, and UL-94 values. The FRI values were calculated by authors of the present review. The name and the percentage of flame retardants are provided in separate columns. “wt.%” was used for loading level of additives, while “―” stands for the systems free of additive or the neat PP. * FR means flame retardant. Since all comparisons were made in terms of FRI, classification of polymers in terms of their flame-retardant properties was not surveyed based on the chemistry of additives, heat flux, sample thickness, etc.

PP Containing Nitrogen-Based (N) FR * wt.% TTI
(s)
pHRR
(kW·m−2)
THR
(MJ·m−2)
Irradiance
(kW·m−2)
Sample Thickness (mm) FRI LOI UL-94 Ref.
44 1175 106 35 3 [63]
Melamine phosphate (MP) 40 39 296 78 35 3 4.78 [63]
54 930 140 35 4 NR [64]
Melamine salt of pentaerythritol phosphate kaolinite (MPPK) 15 30 208 70 35 4 4.96 NR [64]
MPPK 20 28 148 42 35 4 10.86 V-0 [64]
MPPK 25 34 130 33 35 4 19.10 V-0 [64]
30 929 134 50 3 17 NR [65]
Melamine salt of tripentaerythriol phosphate (MTP) 15 22 480 101 50 3 1.88 [65]
MTP 20 22 267 91 50 3 3.75 28 V-1 [65]
MTP 25 22 226 73 50 3 5.53 32 V-0 [65]
MTP 30 22 219 72 50 3 5.78 35 V-0 [65]
Methyl hydrogen siloxane modified MTP (m-MTP) 30 21 253 72 50 3 4.78 30 V-0 [65]
65 1417 128.5 35 3 NR [57]
Melamine pyrophosphate (MPyP) 30 36 437 103.1 35 3 2.23 NR [57]
34 1727 112 35 3 17 NR [66]
MPyP 30 19 511 83 35 3 2.54 25.5 NR [66]
Triazine-based charring foaming agent: synthesized by reaction of cyanuric chloride and ethanolamine and ethylenediamine (TA-CFA) 30 13 584 96 35 3 1.31 24 NR [66]
48 988 88.3 35 3 17 NR [39]
Triazine-based CFA: synthesized by reaction of cyanuric chloride and piperazine (TA-CFA) 30 34 468 86.6 35 3 1.52 20.5 V-1 [39]
50 1350 91.2 35 3 17 NR [40]
Triazine-based CFA: synthesized by polycondensation of 2-chloro-4,6-di-(2-hydroxyethylamino)-s-triazine (TA-CFA) 30 38 518 86.7 35 3 2.08 23.5 NR [40]
45 759.2 98.8 35 3 17 NR [37]
Triazine-based CFA: synthesized from a macromolecular triazine derivative containing hydroxyethylamino and triazine rings and ethylenediamino groups (TA-CFA) 25 34 487.4 91.6 35 3 1.26 21.9 NR [37]
20 809 96 50 3 17.6 NR [32]
Triazine-based CFA: Poly[N4-bis(ethylenediamino)-phenyl phosphonic-N2, N6-bis(ethylenediamino)-1,3,5-triazine-N-phenyl (TA-CFA) 25 12 529 88 50 3 1.00 20.6 NR [32]
18 1457 156 50 3 19 NR [29]
Triazin-based CA—Zinc oxide (TA-CA-ZnO) 25 17 694 149 50 3 2.07 18.3 NR [29]
41 840.3 115.7 35 3 16.4 NR [67]
Triazin-based CA: Poly(ethanediamine-1,3,5-triazine-p-4-amino-2,2,6,6-tetramethylpiperidine) (TA-CA) 25 30 684 106.7 35 3 0.97 17.8 NR [67]
48 1351 107 35 3.2 18.5 NR [27]
Triazin-based CA: compound containing pentaerythritol and triazine structure (TA-CA) 20 42 994 98 35 3.2 1.29 22 NR [27]
66 633 44.2 35 3 17 NR [23]
Triazin-based CA: synthesized by
reaction of tris (2-hydrooxyethyl) isocyanurate and 2-carboxyethyl (phenyl) phosphinic acid (TA-CA)
20 31 417 37.6 35 3 0.83 22 NR [23]
31 1239 123.6 50 3 18.5 NR [68]
Triazin-based IFR: synthesized by
reaction of tris(2-hydroxyethyl) isocyanurate and polyphosphoric acid and melamine (TA-IFR)
20 18 289.9 89 50 3 3.44 29.3 V-0 [68]
48 988 88.3 35 3.2 17 NR [31]
Triazin-based IFR: synthesized by
reaction of cyanuric chloride
and N-amino ethylpiperazine (TA-IFR)
25 38 504 86.6 35 3.2 1.58 23 V-1 [31]
20 904.4 126.2 50 3 18 NR [69]
Piperazine-based FR: synthesized by
reaction of diphenylphosphinyl chloride and piperazine (PI-FR)
25 58 487.7 87.5 50 3 7.75 27 V-0 [69]
45 1269 146.4 50 3 17.5 NR [70]
Piperazine-based IFR: Piperazine spirocyclic phosphoramidate (PI-IFR) 30 17 240.4 120.2 50 3 2.42 30.5 V-0 [70]
47 802 104 35 3 18 NR [71]
Piperazine-based IFR: synthesized by
reaction of phosphorus chloride and 2,6,7-trioxa-l-phosphabicyclo[2,2,2]-octane-4-methanol and anhydrous piperazine (PI-IFR)
20 36 275 78 35 3 2.97 24 NR [71]
Piperazine-based IFR: synthesized by
reaction of phosphorus chloride and 2,6,7-trioxa-l-phosphabicyclo[2,2,2]-octane-4-methanol and anhydrous piperazine (PI-IFR)
30 37 209 74 35 3 4.24 27 NR [71]
Piperazine-based IFR: synthesized by
reaction of phosphorus chloride and 2,6,7-trioxa-l-phosphabicyclo[2,2,2]-octane-4-methanol and anhydrous piperazine (PI-IFR)
40 37 162 60 35 3 6.75 29 V-0 [71]
36 799.3 170.9 35 4 18 NR [72]
N-alkoxy hindered amine (NOR116) 0.5 44 738.8 156.5 35 4 1.44 19 NR [72]
36 799 170 35 4 17.5 NR [73]
NOR116 0.3 44 738 156 35 4 1.44 19.5 NR [73]
42 831 112 35 3 18 NR [50]
Polyurethane containing Phosphorus-based CA (PPU-CA) 25 27.3 475 83 35 3 1.53 29 NR [50]
42 1025 137.7 35 4 [74]
Nitrogen-based FR: compound containing Nitrogen (27.5.wt.%) and Phosphorus (15.6 wt.%) (N-FR) 22 22 170 50.3 35 4 8.64 32 V-1 [74]
Nitrogen-based FR: compound containing Nitrogen (27.5 wt.%) and Phosphorus (15.6 wt.%) (N-FR) 25 21 160 49.1 35 4 8.98 34 V-0 [74]
30 1093 108.2 50 3 18 NR [75]
Nitrogen-based IFR: Poly (diallyldimethylammonium) and polyphosphate polyelectrolyte complexe-based IFR (N-IFR) 5 28 968.5 103.4 50 3 1.10 20.2 NR [75]
Nitrogen-based IFR: Poly (diallyldimethylammonium) and polyphosphate polyelectrolyte complexe-based IFR (N-IFR) 10 25 626.2 97.1 50 3 1.62 22 NR [75]
Nitrogen-based IFR: Poly (diallyldimethylammonium) and polyphosphate polyelectrolyte complexe-based IFR (N-IFR) 15 23 543.1 94.3 50 3 1.76 24.4 NR [75]
Nitrogen-based IFR: Poly (diallyldimethylammonium) and polyphosphate polyelectrolyte complexe-based IFR (N-IFR) 20 21 443.9 90.1 50 3 2.06 26.3 NR [75]
Nitrogen-based IFR: Poly (diallyldimethylammonium) and polyphosphate polyelectrolyte complexe-based IFR (N-IFR) 25 18 335.3 83.9 50 3 2.52 27.5 V-2 [75]
25 874.1 89.3 50 3 18 NR [76]
Nitrogen-based IFR: compound containing Nitrogen (23%) and Phosphorus (21%) (N-IFR) 25 12 94.9 68.2 50 3 5.78 33 V-0 [76]
29 980 136 50 18.5 [56]
Phosphorus and Nitrogene based IFR 30 22 229 93 50 4.74 36.3 [56]