Advances in Materials Science and Engineering

Advances in Materials Science and Engineering / 2013 / Article

Research Article | Open Access

Volume 2013 |Article ID 960914 | https://doi.org/10.1155/2013/960914

Linsheng Tang, Zhigang Yuan, Lu Xu, Xue Li, Yuzhen Ge, "Synergistic Flame Retardancy of Aluminium Dipropylphosphinate and Melamine in Polyamide 6", Advances in Materials Science and Engineering, vol. 2013, Article ID 960914, 8 pages, 2013. https://doi.org/10.1155/2013/960914

Synergistic Flame Retardancy of Aluminium Dipropylphosphinate and Melamine in Polyamide 6

Academic Editor: William A. Jesser
Received21 May 2013
Accepted24 Sep 2013
Published05 Nov 2013

Abstract

The synergistic flame retardancy of aluminium dipropylphosphinate (ADPP) and melamine (ME) in polyamide 6 (PA6) was studied by the limiting oxygen index (LOI) measurement, the vertical burning test, and the cone calorimeter test, and the mechanism was also discussed by thermogravimetric and residual analyses. The experimental results indicated that there was obvious synergistic flame retardancy between ADPP and ME under their appropriate weight ratios. The thermogravimetric results and the analysis of the residues obtained in cone calorimeter test showed that ADPP and ADPP/ME played the role of flame retardance by gaseous- and condensed-phase mechanisms, where, on one hand, they were decomposed into nonvolatile aluminum phosphate and promoted the carbonization of PA6, and the formed intumescent layer resulted in flame retardancy by the barrier effect on heat, air, and decomposition products, and on the other hand, they were decomposed into volatile phosphorus compounds which bring about flame retardancy by flame inhibition. Using a combination of ADPP and ME improved charring of PA6 and raised the residual rate of P and Al, thus, improving the barrier effect in the condensed phase.

1. Introduction

The alkylphosphinates developed by Clariant Company (Germany) belong to a novel class of phosphorous flame retardants. The alkylphosphinates have some merits such as low toxicity and smoke density, high comparative tracking index (CTI), good thermal stability, and being especially used as flame retardants for polyamides, polyesters, and epoxy resins [1]. Some patents reported that alkylphosphinates and nitrogen flame retardants such as melamine derivatives had obvious synergistic flame retardancy in polyamides [26]. However, so far, only very little literatures reported the flame retardancy mechanism and regularity [7, 8], so there is a lack of scientific understanding as to the synergistic flame retardancy regularity and mechanism between alkylphosphinates and nitrogen flame retardants. Thus, the flame retardancy and its mechanisms of aluminium dipropylphosphinate in combination with melamine in polyamide 6 was illumianated in this paper.

2. Experimental

2.1. Materials

Nylon 6 (PA6) was provided by Shijiazhuang Refining & Chemical Co., China. The aluminium dipropylphosphinate (ADPP) was made by ourselves. The melamine was provided by Wujiang City Today Chemical Technology Co., Ltd., China. The antioxidants of 1010 and 168 were provided by Beijing Jiyi Chemical Co., Ltd., China. All materials used in this work were of technical grade and were used without further purification.

2.2. Preparation of Flame-Retarded Samples

PA6, flame retardants, and small amounts of 1010 and 168 antioxidants were mixed at about 230°C in a JS30A twin-screw extruder (YanTai City Qitong Machinery Co., Ltd., China.) with a rotor speed of 20~30 rpm. The well-mixed ingredients were cooled to ambient temperature and were mould-pressed into 100 × 100 × 4 mm sheets at 220°C~230°C under 5 MPa by 2G-10T press vulcanizer (Dongguan Zhenggong Mechanical and Electrical Equipment Technology Co., Ltd., China). The sheets were then cut into standard samples (100 × 13 × 4 mm3 and 100 × 6.5 × 4 mm3) for flame retardant test.

2.3. Flame Retardant Test

Limiting oxygen index (LOI) was measured according to ASTM D 2863 with a JF-3 oxygen index meter (Jiangning Analytical Instrument Company, China). The specimens used for the LOI test were of dimensions of 100 × 6.5 × 4 mm3.

The vertical burning test was carried out on CZF-3 horizontal and vertical burning tester (Jiangning Analytical Instrument Company, China) with specimens of 100 × 13 × 4 mm3 according to the UL 94 test standard.

The fire behavior of PA6 and flame-retarded PA6 for flaming conditions was characterized according to ISO5660 using an FTT standard cone calorimeter (FTT Company, UK) in external heat fluxes of 50 kw/m2 with specimens of 100 × l00 × 4 mm3. This method enabled investigation with respect to heat release rate (HRR), total heat release (THR), and mass loss rate (MLR).

2.4. Thermogravimetric Analysis

Thermogravimetric (TG) experiments were performed using SDT Q600 thermogravimetric analyzer (TA Company, USA) with a heating rate of 10°C/min and nitrogen flow of 50 mL/min.

2.5. Characterization of the Residue

The surface morphology of the residue obtained in the cone calorimeter test was observed by scanning electron microscopy (SEM, Model JSM-6700F Jeol, Japan).

IR spectra of the residue were measured by potassium bromide pellet technology using a TENSOR-27 IR spectrometer (Bruker Corporation, Germany).

31P NMR spectra were acquired with an Advance 500 spectrometer (Bruker Corporation, Germany) with D2O as a solvent, and 31P chemical shifts were referenced to phosphoric acid (  ppm).

The content of nitrogen was measured by the method of Kjeldahl nitrogen determination [9].

The content of phosphorous was measured by the method of gravimetric quimociac method [10].

The content of aluminum was measured by the EDTA titration method [11].

3. Results and Discussion

3.1. The LOI and Vertical Burning Property

As the loading of flame retardants was 25 wt% based on the total weight of the composites, effect of the formulation of the combinations of ADPP and ME was investigated. As could be seen in Table 1, the weight ratios of ADPP to ME had significant impact on the LOI and vertical burning property of the flame-retarded PA6. The LOI of the flame-retarded PA6 increased firstly with the increase of the proportion of ME, and as the weight ratios of ADPP to Me were 75 : 25~45 : 55, the LOI changed slightly then decreased with the increasing ratios of ME. However, there was not obvious influence of the proportion of ME on the UL 94 classification; all samples reached FV-0 class during 100 : 0~25 : 75 of the weight ratios of ADPP to ME. The LOI of the flame-retarded PA6 alone with ADPP could be up to 33.2%, and the demanding V-0 classification of the burning test could be achieved, while the LOI of the flame-retarded PA6 with ME was 28.3%, and any classification of the burning test could not be reached, which revealed that the flame retardancy of ADPP was markedly better than that of ME in PA6.


(ADPP) :  (ME)LOI/%UL 94 classCombustion phenomenon

100 : 033.2FV-0Difficult ignition, self-extinguishing, no drips
85 : 1535.4FV-0Difficult ignition, self-extinguishing, no drips
75 : 2536.3FV-0Difficult ignition, self-extinguishing, no drips
65 : 3536.4FV-0Difficult ignition, self-extinguishing, no drips
55 : 4536.5FV-0Difficult ignition, self-extinguishing, no drips
45 : 5536.6FV-0Difficult ignition, self-extinguishing, no drips
35 : 6535.2FV-0Difficult ignition, self-extinguishing, no drips
25 : 7534.0FV-0Difficult ignition, self-extinguishing, no drips
15 : 8531.1FV-1Gentle combustion, self-extinguishing, no drips
0 : 10028.3Sustained combustion, later severe, drips

In order to further confirm the synergistic flame retardancy between ADPP and ME, the effect of the loading of flame retardants on the LOI and vertical burning property of the flame-retarded PA6 was, respectively, investigated under 100 : 0, 75 : 25, 25 : 75, and 0 : 100 of the weight ratios of ADPP to ME, and the results were shown in Table 2.


(ME) :  (ADPP)Loading/% LOI/%UL 94 classCombustion phenomenon

0 : 100022.5Sustained combustion, drips
526.8Sustained combustion, drips
1029.8FV-1Gentle combustion, self-extinguishing, no drips
1530.7FV-0Difficult ignition, self-extinguishing, no drips
2032.2FV-0Difficult ignition, self-extinguishing, no drips
2533.2FV-0Difficult ignition, self-extinguishing, no drips

25 : 75528.7Sustained combustion, drips
1030.9FV-0Difficult ignition, self-extinguishing, no drips
1531.8FV-0Difficult ignition, self-extinguishing, no drips
2034.7FV-0Difficult ignition, self-extinguishing, no drips
2536.3FV-0Difficult ignition, self-extinguishing, no drips

75 : 25528.0Sustained combustion, drips
1028.8Sustained combustion, drips
1529.8Sustained combustion, drips
2030.3FV-1Gentle combustion, self-extinguishing, no drips
2534.0FV-0Difficult ignition, self-extinguishing, no drips

100 : 0523.5Sustained combustion, drips
1024.1Sustained combustion, drips
1526.7Sustained combustion, drips
2027.6Sustained combustion, drips
2528.3Sustained combustion, drips

As could be seen in Table 2, the LOI of PA6 without flame retardant was 22.5%, and any classification could not be reached. The LOI of the flame-retarded PA6 alone with 15 wt% of the loading of ADPP could be up to 30.7%, and the demanding V-0 classification of the burning test could be achieved, which indicated that ADPP had good flame retardancy in PA6. As the weight ratio of ADPP to ME was 75 : 25 and the loading of the combination was 10 wt% based on the total weight of the composites, the LOI of the flame-retarded PA6 could be up to 30.9%, and the demanding V-0 classification of the burning test could be achieved. However, as the weight ratio of ADPP to ME was 25 : 75, only when the dosage of the combination is 25 wt%, the demanding V-0 classification could be achieved. The LOI of the flame-retarded PA6 alone with 25 wt% of the dosage of ME was 28.3%, and any classification could not be reached, which indicated that ME had poor flame retardancy in PA6. Thus, it could be seen that there was obvious synergistic flame retardancy between ADPP and ME under their appropriate weight ratios.

3.2. Fire Behavior: Heat Release and Mass Loss

HRR, MLR, and THR of PA6 and the flame-retarded PA6 were, respectively, illustrated in Figures 1, 2, and 3. It could be clearly seen that the HRR, MLR, and THR of PA6 increased rapidly after ignition; the curve of HRR was characterized by a sharp peak with 1013 kw/m2 of maximum heat release rate in the burning of 194 s; PA6 was burned perfectly in 450 s. Compared with PA6, the HRR, MLR, and THR of the flame-retarded PA6 alone with 25 wt% of the loading of ME also increased rapidly after ignition, but its curve of HRR was sharper with 1119 kw/m2 of maximum heat release rate in the burning of 185 s, and it was burned perfectly in 345 s, which revealed no flame retardancy of ME. The HRR, MLR and THR of the flame-retarded PA6 alone with 25 wt% of the loading of ADPP increased slowly after ignition; the curve of HRR was characterized by a wider peak; the maximum heat release rate and mass lose rate reduced markedly; the heat release rate was maintained at 200–469 kw/m2 during the burning of 115 s–445 s; the time for complete combustion was 550 s, but the total heat release increased slightly, which suggested slower combustion. The HRR, MLR, and THR curves of the flame-retarded PA6 with 25 wt% of dosage of ADPP/ME (the weight ratio of ADPP/ME was 75 : 25) were similar with those of the aforementioned flame-retarded PA6 with ADPP, but the maximum heat release rate and mass lose rate of the former were smaller, HRR curve was broader, and the time for complete combustion was longer, which further confirmed synergistic flame retardancy between ADPP and ME in PA6.

3.3. Fire Retardancy Mechanisms

The flame retardancy mechanism of ADPP/ME in PA6 was discussed by the residual analysis and thermogravimetric analysis of the flame retardants and the flame-retarded PA6.

3.3.1. Thermogravimetric Analysis

Thermogravimetric results of flame-retardants and flame retarded PA6 were presented in Figures 4, 5, 6, and 7 and Table 3. As could be seen in Figure 4 and Table 3, the initial thermal decomposition temperatures (the temperature for 2% of mass loss) of ADPP and ME were, respectively, 315.8°C and 237.6°C, and subsequently the mass loss of ADPP was smaller than that of ME under the same temperature. The complete thermolysis temperatures of ADPP and ME were, respectively, 500°C and 325°C, and their mass percentages of the resulting residues under the above temperatures were, respectively, about 14 wt% and 0 wt%, which was because ADPP was decomposed into nonvolatile aluminum phosphate, while ME was decomposed into volatile N2 and CO2. The initial thermal decomposition temperature of 75 wt% ADPP/25 wt% ME was 230.7°C, and the decomposition temperatures for 5% and 10% of mass loss were, respectively, 248.1°C and 262.6°C, obviously lower than those of ADPP and ME for the same mass loss. However, when the mass loss was more than about 20%, the decomposition temperature of 75% ADPP/25% ME was between ADPP and ME, and the mass loss of the ADPP/ME was larger than their additive value (supposing no interaction between ADPP and ME), below 370°C and over 440°C, while the results come over in the range of 320°C to 420°C, which implied that there was an obvious interaction between ADPP and ME and that ADPP and ME could promote mutually the decomposition below 370°C and over 440°C but could retard mutually the decomposition in the range of 320°C to 420°C.


MaterialsMass loss
2%/°C5%/°C10%/°C50%/°C

PA6333.6°C386.1°C402.6°C450.1°C
ADPP315.8342.3358.8413.6
ME237.6252.7265.3298.5
ADPP/ME*230.7248.1262.6407.4
Flame-retarded PA6 with 25 wt% ADPP309.7°C328.4°C346.9°C445.0°C
Flame-retarded PA6 with 25 wt% ME268.9°C313.5°C345.9°C418.5°C
Flame-retarded PA6 with 25 wt% ADPP/ME*241.3°C317.2°C349.2°C443.4°C

Mass ratio of ADPP/Me was 75/25.

As could be seen in Figure 5 and Table 3, PA6 was initially decomposed in 333.9°C (the temperature for 2% mass loss), rapidly over 402.6°C, and almost completely in 490°C without any residue, which meant that PA6 was extremely difficult to be carbonized. The flame-retarded PA6 with 25 wt% of ADPP was initially decomposed in 309.7°C, and the decomposition temperatures for 5% and 10% of mass loss were, respectively, 328.4°C and 346.9°C, obviously lower than those of PA6 with the same mass loss, which suggested that the addition of ADPP cut down the thermal stability of PA6. Compared with the additive curves of 75% PA6 and 25% ADPP (supposing no interaction between PA6 and ADPP), the mass loss of the flame-retarded PA6 with ADPP was larger and significantly below 470°C, which indicated that there was a mutually promoted decomposition between PA6 and ADPP but contrariy over 470°C and that the residual rate in 700°C was 23%, indicating improved charring of PA6 by ADPP.

It could be seen from Figure 6 and Table 3 that the decomposition temperatures of the flame-retarded PA6 with 25 wt% of ME for 2%, 5%, and 10% of mass loss were, respectively, 268.9°C, 313.5°C, and 345.9°C, obviously lower than those of the flame-retarded PA6 with 25 wt% of ADPP under the same mass loss, which suggested that the addition of ME reduced more seriously the thermal stability of PA6 than ADPP.

The mass loss of the flame-retarded PA6 with ME was lower than the additive values below 400°C, which implied that there was a mutual stabilization between PA6 and ME but contrariy from 400°C to 480°C and that the residual rate in 500°C was 18%, indicating improved charring of PA6 by ME.

The decomposition temperatures of the flame-retarded PA6 with 25 wt% of the combination with 75/25 of the weight ratio of ADPP/ME for 2% and 5% mass loss were, respectively, 241°C and 317°C, close to those of the flame-retarded PA6 with ME, while the decomposition temperature for more than 10% of mass loss was close to those of the flame-retarded PA6 with ADPP. Thus, it could be seen that ADPP/ME had great impact on the thermal stability of the materials. The mass loss of the flame-retarded PA6 with ADPP/ME was nearly the same as their additive value below 430, but it was obviously larger in the range of 430°C~490°C, and the residual rate was also apparently larger than the additive value, which indicated a mutual promoted decomposition between PA6 and ADPP/ME and improved charring of PA6 by ADPP/ME.

3.3.2. Analysis of the Residues Obtained in Cone Calorimeter Test

As could be seen in the photos of residues obtained in cone calorimeter test shown in Figure 8, the residues of PA6 and the flame-retarded PA6 with ME were obviously less than those of the flame-retarded PA6 with ADPP and ADPP/ME, and the former did not form the intumescent char layer, while the latter did.

The SEM pictures (Figure 9) of the residues obtained in the cone calorimeter showed that the smooth and dense layers were formed after the combustion of the flame-retarded PA6 with ADPP and ADPP/ME, which brought about the flame retardancy by the barrier effect on heat, air, and decomposition products.

As could be seen in Figure 10, the IR spectra of the residue of the flame-retarded PA6 with ADPP were similar to those of ADPP/ME. 1130 cm−1 (P=O) and 490 cm−1 (P–O or Al–O) were characteristic bands of aluminum phosphate. The band around 1600 cm−1 was attributed to carbon-oxygen signals from PA6 residue.

As could be seen in Figure 11, the 31P NMR spectra of the residue of the flame-retarded PA6 with ADPP dissolved with 10 wt% sodium hydroxide solution were similar to those of ADPP/ME. The main signal points to a dominant production of sodium phosphate (aluminium phosphate was converted into sodium phosphate in the presence of sodium hydroxide), due to its position at around 6 ppm.

The above IR spectra and 31P NMR spectra revealed that ADPP was partially converted into aluminum phosphate in the process of combustion.

The residual rate of samples, the content, and the residual rate of P and Al in the residues obtained in the cone calorimeter test were illustrated in Table 4.


SamplesResidue/%PAlN/%
Content/%Residue/%Content/%Residue/%

PA60.50Trace amount
Flame-retarded PA6 with ADPP3.5418.513.414.736.5Trace amount
Flame-retarded PA6 with ME0.42Trace amount
Flame-retarded PA6 with ADPP/ME4.7517.422.514.062.2Trace amount

As could be seen in Table 4, the residual rate of PA6 and the flame-retarded PA6 with ME was less than about 0.5 wt% and was significantly lower than that of the flame-retarded PA6 with ADPP and ADPP/ME, but the latter two were only, respectively, 3.54 wt% and 4.75%, which indicated that the charring of the flame-retarded PA6 with ADPP and ADPP/ME was better than that of PA6 and the flame-retarded PA6 with ME, but it was not good enough. The above residual rates were conspicuously different from the thermogravimetric results, which might be attributed to the different thermal conditions. The residual rate of P and Al in the residues was also lower, which implied that most of the decomposition products of aluminium dipropylphosphinate vaporized to gaseous phase in the process of combustion. Thus, it could be seen that ADPP and ADPP/ME played the flame retardancy by gaseous- and condensed-phase mechanisms, where, on one hand, they were decomposed into nonvolatile aluminum phosphate and promoted the carbonization of PA6, and the formed intumescent layer resulted in flame retardancy by the barrier effect on heat, air, and decomposition products, and on the other hand, they were decomposed into volatile phosphorus compounds which bring about flame retardancy by flame inhibition. Using a combination of ADPP and ME improved charring of PA6 and raised the residual rate of P and Al, thus, improving the barrier effect in the condensed phase.

4. Conclusion

There was obvious synergistic flame retardancy between ADPP and ME under their appropriate weight ratios. As the weight ratio of ADPP to ME was 75 : 25 and the loading of the combination is 10 wt% based on the total weight of the composites, the LOI of the flame-retarded PA6 could be up to 30.9%, and the demanding V-0 classification of the burning test according to the UL 94 standard could be achieved, which were the same as alone with 15% of the amount of ADPP, but any classification could not be reached alone with 25% of the amount of ME. Compared with flame-retarded PA6 with ADPP, the maximal heat release rate (HRR) and mass loss rate (MLR) of flame-retarded PA6 with ADPP/ME were smaller, and the curves of HRR-combustion time and MLR-combustion time were broader. The thermogravimetric results and the analysis of the residues obtained in cone calorimeter test showed that ADPP and ADPP/ME played the role of flame retardance by gaseous- and condensed-phase mechanisms, where, on one hand, they were decomposed into nonvolatile aluminum phosphate and promoted the carbonization of PA6, and the formed intumescent layer resulted in flame retardancy by the barrier effect on heat, air, and decomposition products, and on the other hand, they were decomposed into volatile phosphorus compounds which bring about flame retardancy by flame inhibition. Using a combination of ADPP and ME improved charring of PA6 and raised the residual rate of P and Al, thus, improving the barrier effect in the condensed phase.

Acknowledgment

This work is financially supported by Shandong Provincial Natural Science Foundation with Grant no. ZR2012BM017.

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Copyright © 2013 Linsheng Tang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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