2,366
Views
14
CrossRef citations to date
0
Altmetric
Short Communication

Flame retardant and smoke-suppressant rigid polyurethane foam based on sodium alginate and aluminum diethylphosphite

ORCID Icon, &
Pages 46-52 | Received 15 Dec 2020, Accepted 18 Jan 2021, Published online: 31 Jan 2021

ABSTRACT

In order to improve the flame-retardant effect and thermal behaviour of rigid polyurethane foam (RPUF), the flame retardancy of sodium alginate (SA), aluminium diethyl phosphite (ADPO2) and expandable graphite (EG) were proposed. First, the structures of RPUF with or without flame retardancy were confirmed by scanning electron microscopy (SEM). Additionally, the combustion behaviours and thermal performance of the flame-retardant polyurethane were evaluated through thermogravimetric analysis (TGA), limiting oxygen index (LOI) tests, and UL-94 tests. Finally, the cone calorimeter results reveled the RPUF/5ADPO2/7.5SA/7.5EG exhibit excellent thermodynamic properties. The results of the heat release rate (HRR), total heat release (THR), total smoke production (TSP), and smoke production rate (SPR) could demonstrate the smoke-suppressant and flame-retardant of polyurethane. The system of RPUF/ADPO2/SA/EG showed excellent flame-retardant in polyurethane.

1. Introduction

Rigid polyurethane foam (RPUF) is a material with one of the best thermal insulation effects in the world. Due to its good thermal insulation performance, cold resistance, anti-corrosion, heat insulation, high strength, lightweight and other excellent characteristics, rigid polyurethane foam has become an indispensable material for heat insulation, water-proofing, leak stoppage, and for use in different industrial sectors, such as construction, transportation, the chemical industry, refrigeration, and power [Citation1,Citation2,Citation12-14]. However, pristine RPUF had poor flame-retardant properties; in particular, there was a source of fire, RPUF burned smoothly, and the flame spread rapidly and generated a large amount of smoke [Citation16-19]. Therefore, it is essential to study the flame retardancy of RPUF to protect the safety of people’s lives and property.

Lei Liu et al. used nano zirconium amino-tris-(methylenephosphonate) and expandable graphite to modify the flame retardant, mechanical and thermal insulating properties of rigid polyurethane foam [Citation3]; Sheng Xu et al. have shown the synergistic flame-retarding effect of alginate and layered double hydroxides [Citation4]. Zhang et al. have shown the flame retardant of ADPO2 and EG [Citation5]; SA has been used by other researchers to the flame-retardant effect in other fields [Citation6,Citation7]. No studies have shown that the sodium alginate (SA)/aluminium diethylphosphite (ADPO2)/expandable graphite (EG) system could react with polyurethane foam to achieve a better flame-retardant effect. In the manuscript, the synergies gained from SA, ADPO2 and EG would exhibit a great smoke suppression and flame-retardant in polyurethane.

2. Materials and methods

Polyether polyol (hydroxyl number: 54.5–58.5 mg/g; viscosity: 7000 mpa·s/25°C) was purchased from Guangzhou Huixiang Chemical Industry Co., Ltd. (Guangdong, China). Diphenylmethane diisocyanate (MDI; technical pure grade) was purchased from Jinan Dada Chemical Industry Co., Ltd. (Shandong, China). Expandable graphite (particle size: 1000 mesh; carbon content: 99.996%) was supplied by Henan Liugong Graphite Co., Ltd. (Henan, China). Aluminium diethyl phosphite (density at 20°C: 1.35 g/m3; particle size: 20 ~ 40 μm) was supplied by Shanghai Suisi Chemical Technology Co., LTD. Sodium alginate (SA; white powder; pH: 6–8; granularity: 100 mesh; viscosity: 100–800 mpa·s) was purchased from Shandong Xiangyu Biotechnology Co., LTD. The stabilizer (technical pure grade) was supplied from Shanghai Baiang Chemical Technology Co., Ltd. (Shanghai, China) [Citation8].

All of the RPUF were prepared by box foaming (size: 100 mm×100 mm×10 mm). First, SA or ADPO2 was separately introduced into mould with RPUF, stirred for 30 s, held until foaming stabilization, then put into a drying oven, dried for 30 min at 80°C, and allowed to stand for 24 h at 25°C. Then, SA and ADPO2 were introduced to polyether polyol at the same time, stirred to mix well, and combined with MDI (with or without EG), stirred for 30 s, held until foaming stabilization in the box foaming, put into a drying oven, dried for 30 min at 80°C, and allowed to stand for 24 h at 25°C, as . The combustion conditions of different samples were compared, and the ratio of SA to ADPO2 was adjusted () to obtain the best flame-retardant effect.

Table 1. LOI values and UL-94 grades of different component samples

Figure 1. Production flow chart of RPUF/7.5SA/5ADPO2/5EG

Figure 1. Production flow chart of RPUF/7.5SA/5ADPO2/5EG

A scanning electron microscope (SEM, FEI Nova Nano SEM 430) was used to observe the internal structure of the samples. Thermogravimetric analysis (TGA; STA8000 thermal gravimetric analyzer; Perkin Elmer) was used to measure the mass of the sample in relation to its temperature [Citation9]. Each sample was measured under a nitrogen atmosphere with a 10°C/min rate from 0°C to 600°C. Samples with a size of 100 mm×100 mm×10 mm were prepared to test the Limit Oxygen Index (LOI) using a Fire Testing Technology (Germany Eager Technology Inc.), according to the ASTM D2863-19 standard. An FTT cone calorimeter was used to characterize the fire behaviour according to ISO 5660. The dimensions of the samples were 100 mm×100 mm×10 mm. The measured parameters included the heat release rate (HRR, kW/m2), total heat release (THR, MJ/m2), and total smoke release (TSR, m2/m2) [Citation10].

3. Results and discussion

3.1 Morphology characterization

To further explore the change in internal structure resulting from the addition of SA and ADPO2 to polyurethane, the internal structure of polyurethane was observed by scanning electron microscopy, as shown in . shows the internal structure of the rigid polyurethane foam without flame retardant had large gaps. During burning, heat would be instantaneously transferred through these large gaps, resulting in an acceleration in burning speed. Apparently, the internal gap structure of RPUF with 7.5SA/5ADPO2 decreased than the pristine RPUF (). As shown in , when SA and ADPO2 were added to the mixed polyurethane, the internal structure was denser. With the amount of EG increasing, and the inner space of 7.5SA/5ADPO2/5EG became more compact than 7.5SA/5ADPO2. However, the SEM characterization of 7.5SA/5ADPO2/5EG () was similar to 7.5SA/5ADPO2/7.5EG (). EG, as additive hard particles, would affect the bubble nucleation and bubble growth during the foaming process, further to damage the foam structure [Citation11]. The addition of EG resulted in the collapse of large cell size and collapse cellular structure [Citation8]. The system of SA/ADPO2/EG can have a synergistic effect that prevents further combustion after the reaction.

Figure 2. SEM images of various samples (a: pure RPUF; b: RPUF/7.5SA/5ADPO2; c: RPUF/7.5SA/5ADPO2/5EG; d: RPUF/7.5SA/5ADPO2/7.5EG)

Figure 2. SEM images of various samples (a: pure RPUF; b: RPUF/7.5SA/5ADPO2; c: RPUF/7.5SA/5ADPO2/5EG; d: RPUF/7.5SA/5ADPO2/7.5EG)

3.2 Flame retardancy

The combustion state of the sample, heated at the bottom, was observed at 1, 5 and 15 s, as shown in . When SA and ADPO2 were introduced into RPUF, the flame went out within 5S after the ignition source left, and the carbonization degree was reduced. LOI measuring instrument was determined the volume percentage of oxygen required during polymer combustion, and the flammability of the sample was tested by UL-94 vertical combustion tester. The results are shown in , and the standard deviation and standard error values were ±0.1%. The LOI of RPUF with SA (RPUF/12.5SA) increased from 17.0% (pristine RPUF) to 19.0%. The LOI value of RPUF with SA and ADPO2 (RPUF/5ADPO2/7.5SA) was 21.5%, higher than that of RPUF/6.25ADPO2/6.25SA and RPUF/3.1ADPO2/9.4SA.

Figure 3. Combustion of different samples at different times (a:pure RPUF;b:RPUF/7.5SA/5ADPO2;c: RPUF/7.5SA/5ADPO2/2.5EG;d: RPUF/7.5SA/5ADPO2/5EG; e: RPUF/7.5SA/5ADPO2/7.5EG f: RPUF/3.75SA/2.5ADPO2/5EG;g: RPUF/7.5SA;h: RPUF/7.5SA/5EG)

Figure 3. Combustion of different samples at different times (a:pure RPUF;b:RPUF/7.5SA/5ADPO2;c: RPUF/7.5SA/5ADPO2/2.5EG;d: RPUF/7.5SA/5ADPO2/5EG; e: RPUF/7.5SA/5ADPO2/7.5EG f: RPUF/3.75SA/2.5ADPO2/5EG;g: RPUF/7.5SA;h: RPUF/7.5SA/5EG)

According to the orthogonal method, the ratio of SA to ADPO2 was adjusted (). The combustion degree of the sample with a rate of SA to ADPO2 of 1:2 was less than 1:1. Upon adjusting the rate to 3:1 and 3:2, the latter rate had the best result. Based on these results, by adding EG, the flame-retardant effect was obviously increased, and the LOI of RPUF/5ADPO2/7.5SA/2.5EG, RPUF/5ADPO2/7.5SA/5EG and RPUF/5ADPO2/7.5SA/7.5EG was higher than those of RPUF/5ADPO2/7.5SA and pristine RPUF, and the UL-94 rating reached V0 without any dripping. However, compared with RPUF/5ADPO2/7.5SA/7.5EG, the flame-retardant effect of RPUF/5ADPO2/7.5SA/5EG was almost the same, and the increase in LOI was not apparent. Therefore, it was clear that at an ADPO2:SA:EG ratio of 2:3:3, the LOI value was the highest, and the UL-94 level was the highest.

The system of SA/ADPO2/EG has a synergistic flame-retardant effect. Although the flame-retardant effect of RPUF with SA (RPUF/12.5SA) was similar to that of RPUF with SA and EG (RPUF/7.5SA/5EG), the synergistic flame-retardant effect of only SA and EG was not obvious. When EG was introduced into RPUF with SA and ADPO2, the carbonized area of combustion was smaller, and the flame-retardant effect was much better than only adding SA and EG ( g). When burned, the internal network structure of polyurethane was filled and shrunk, and there were many phosphorus elements distributed in the structure. When the sample was ignited, a layer of carbon layer formed on the surface, and the surface gap would be filled to prevent the further spread of flame to the interior as shown in . The system of SA/ADPO2/EG could have an excellent flame-retardant effect on RPUF.

Figure 4. Combustion diagram of polyurethane internal network structure

Figure 4. Combustion diagram of polyurethane internal network structure

3.3 TGA tests

The Thermal decomposition behaviour of RPUF was analyzed by thermogravimetric analysis instrument [Citation8]. The TGA data of the various samples are shown in . Below 250°C, the behaviours of the samples were nearly the same. At 220°C and 335°C, pure RPUF achieved T5% and T50%.the synergistic effect of ADPO2 and SA made the RPUF/5ADPO2/7.5SA temperature of T5% and T50% delayed at about 240°C and 355°C. Over 300°C, pure RPUF decreased faster, only about 20% of the weight was left at 600°C, while RPUF/5ADPO2/7.5SA/5EG and RPUF/5ADPO2/7.5SA/7.5EG obviously showed that this system of SA/ADPO2/EG had a superior effect, and its weight loss rate was about 42%. The residue weight of RPUF/7.5SA/5EG with the same amount of EG was significantly lower than that of RPUF/5ADPO2/7.5SA/5EG. The residue weight of RPUF/5ADPO2/7.5SA/2.5EG was about 31% and about 42% of RPUF/5ADPO2/7.5SA/5EG. The residue weight of RPUF/2.5ADPO2/3.75SA/5EG was a little higher than RPUF/5ADPO2/7.5SA and RPUF7.5SA/5EG, which mean the system of SA/ADPO2/EG was better than RPUF with two kinds of them. This behaviour can be analyzed from the perspective that the treated RPUF has a composite structure composed of the hard cell structure and soft regions [Citation8].

Table 2. TGA data of the various samples

3.4 Cone calorimeter

HRR, THR, SPR and TSP were explored to evaluate the smoke and fire risk of the materials [Citation3]. From , the combustion speed of the pristine RPUF was very fast, until the whole area was carbonized, it would stop burning. The peak heat release rate (PHRR) was 155 kW/m2, while the PHRR of RPUF/5ADPO2/7.5SA/7.5EG decreased by 22.6%. The THR value of RPUF/5ADPO2/7.5SA/7.5EG was approximately 6 MJ/m2. For SPR, RPUF/5ADPO2/7.5SA/7.5EG yielded the lowest value, while the TSP of RPUF/5ADPO2/7.5SA/7.5EG and RPUF/7.5SA/5EG was lower than that of RPUF. The PHRR of RPUF/5ADPO2/7.5SA/5EG and RPUF/2.5ADPO2/3.75SA/5EG could achieve 125 and 140 kW/m2; however, the PHRR of the sample without EG or little EG was higher than pure RPUF. ADPO2 and SA could not contribute to the decrease of HRR and THR. The synergistic effect of ADPO2/SA/EG could decrease the PHRR. Considered the charring ability of RPUF/5ADPO2/7.5SA/5EG, the residue weight was the highest. It can explain that the char residues formed during the combustion and prevent the transfer of heat and oxygen [Citation15,Citation20,Citation21]. Additionally, the peak SPR of RPUF/5ADPO2/7.5SA/5EG was 0.06 m2, the lowest of all. The peak SPR of RPUF/5ADPO2/7.5SA/5EG and pure RPUF was similar. The TSP of RPUF/5ADPO2/7.5SA/5EG was lower than pure RPUF before the combustion time of 40 s; however, after 40 s, the TSP of RPUF/5ADPO2/7.5SA/5EG was higher than pure RPUF. The TSP of RPUF/7.5SA/5EG was the lowest. SA and EG contributed to the decrease in smoke. ADPO2 mainly contributed flame retardancy via promoting the formation of phosphorus-containing compounds in gas, leading to more smoke release [Citation8]. During combustion, EG plays an important role in the flame retardant and smoke suppression. However, the synergistic flame retardant and smoke suppression effect of ADPO2/SA/EG was the best.

Figure 5. HRR and THR curves of different RPUF foam (a: HRR; b: THR;)

Figure 5. HRR and THR curves of different RPUF foam (a: HRR; b: THR;)

Figure 6. SPR and TSP curves of different RPUF foam (a: SPR; b: TSP)

Figure 6. SPR and TSP curves of different RPUF foam (a: SPR; b: TSP)

4. Conclusions

When the flame retardancy of ADPO2/SA/EG was introduced into RPUF, a layer of carbon layer formed, and the net structure was changed [Citation3]. The system of RPUF/7.5ADPO2/5SA/7.5EG showed excellent flame-retardant properties and smoke suppression compared with pristine RPUF, which decreased the value of PHRR to 125 kw/m2 and the THR was about 6MJ/m2, much lower than pure RPUF. The TSP of RPUF/7.5ADPO2/5SA/7.5EG was 1.5 m2/m2, while the TSP of RPUF/7.5SA/5EG was the lowest (0.8 m2/m2), which exhibit excellent smoke suppression. The LOI value of RPUF/7.5SA/5EG increased to 25.5% and the level of it could reach V0 by UL-94 test. The system of RPUF/ADPO2/SA/EG commonly used as insulation material in buildings showed excellent thermal properties, which could play an excellent role in the field of flame-retardant.

Acknowledgement

This work was supported by the project of young scientific and technological talent program supported by Liaoning Provincial Department of Education (No: LG202030).

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This work was supported by the Young Scientific and Technological Talent Program Supported by Liaoning Provincial Department of Education (No: LG202030) [LG202030].

References

  • Luo F, Kun W, Yinwen L, et al. Reactive flame retardant with core-shell structure and its flame retardancy in rigid polyurethane foam. J Appl Polym Sci. 2015;132(46):46.
  • Lorenzetti A, Modesti M, Gallo E, et al. “Synthesis of phosphinated polyurethane foams with improved fire behaviour”. Polym Degrad Stab. 2012;97(11):2364–2369.
  • Liu L, Wang Z, Zhu M. “Flame retardant, mechanical and thermal insulating properties of rigid polyurethane foam modified by nano zirconium amino-tris-(methylenephosphonate) and expandable graphite ”. Polym Degrad Stab. 2019;170:108997.
  • Sheng X, Si-Yu L, Zhang M, et al. “Fabrication of green alginate-based and layered double hydroxides flame retardant for enhancing the fire retardancy properties of polypropylene”. Carbohydr Polym. 2020;234:115891.
  • Zhang W, Lei Y, Xuetian L, et al. “A facile, environmentally and friendly flame-retardant: synergistic flame retardant property of polyurethane rigid foam”. Mater Lett. 2020;267:127542.
  • Ningjing W, Niu F, Lang W, et al. ”Highly efficient flame-retardant and low-smoke-toxicity poly(vinyl alcohol)/alginate/montmorillonite composite aerogels by two-step crosslinking strategy”. Carbohydr Polym. 2019;221:221–230.
  • Xiaowei M, Yuan B, Pan Y, et al. “A single α-cobalt hydroxide/sodium alginate bilayer layer-by-layer assembly for conferring flame retardancy to flexible polyurethane foams”. Mater Chem Phys. 2017;191:52–61.
  • Rao W-H, Liao W, Wang H, et al. “Flame-retardant and smoke-suppressant flexible polyurethane foams based on reactive phosphorus-containing polyol and expandable graphite”. J Hazard Mater. 2018;360:651–660.
  • Xi W, Qian L, Huang Z, et al. “Continuous flame-retardant actions of two phosphate esters with expandable graphite in rigid polyurethane foams”. Polym Degrad Stab. 2016;130:97–102.
  • Chen Y, Linshan L, Lifeng X, et al. .” Phosphorus-containing silica gel-coated ammonium polyphosphate: preparation, characterization, and its effect on the flame retardancy of rigid polyurethane foam”. J Appl Polym Sci. 2018;135(22):46332.
  • Chen M-J, Shao Z-B, Wang X-L, et al. “Halogen-free flame-retardant flexible polyurethane foam with a novel nitrogen–phosphorus flame retardant”. Industrial & Engineering Chemistry research.. 2012;51(29):9769–9776.
  • Rao W-H, Hua-Xiu X, Ying-Jun X, et al. “Persistently flame-retardant flexible polyurethane foams by a novel phosphorus- containing polyol”. Chem Eng J. 2018;343:198–206.
  • Jian R-K, Chen L, Chen S-Y, et al. “A novel flame-retardant acrylonitrile-butadiene-styrene system based on aluminum isobutylphosphinate and red phosphorus: flame retardance, thermal degradation and pyrolysis behavior”. Polym Degrad Stab. 2014;109:184–193.
  • Mestry S, Kakatkar R, Mhaske ST. “Cardanol derived P and Si based precursors to develop flame retardant PU coating”. Prog Org Coat. 2019;129:59–68.
  • Wang X, Qian L, Huang Z, et al. “Continuous flame-retardant actions of two phosphate esters with expandable graphite in rigid polyurethane foams”. Polym Degrad Stab. 2016;130:97–102.
  • Liu Y, Jiyu H, Yang R. “Effects of dimethyl methylphosphonate,aluminum hydroxide, ammonium polyphosphate, and expandable graphite on the flame retardancy and thermal properties of polyisocyanurate–polyurethane foams”. Ind Eng Chem Res. 2015;54(22):5876–5884.
  • Wang S, Du X, Jiang Y, et al. “Synergetic enhancement of mechanical and fire-resistance performance of waterborne polyurethane by introducing two kinds of phosphorus–nitrogen flame retardant”. J Colloid Interface Sci. 2019;537:197–205.
  • Alongi J, Malucelli G. “Cotton fabrics treated with novel oxidic phases acting as effective smoke suppressants”. Carbohydr Polym. 2012;90(1):251–260.
  • Wang D-Y, Liu Y, Ge X-G, et al. Effect of metal chelates on the ignition and early flaming behaviour of intumescent fire-retarded polyethylene systems. Polym Degrad Stab. 2008;93(5):1024–1030.
  • Liu Y, He J, Yang R. “The synthesis of melamine-based polyether polyol and its effects on the flame retardancy and physical–mechanical property of rigid polyurethane foam”. Journal of Materials Science.. 2017;52(8):4700–4712.
  • Liao H, Hongying L, Liu Y, et al. ”A flame retardant composite foam: foaming polyurethane in melamine formaldehyde foam skeleton”. Poly Int. 2018;68(3):410–417.