Synthesis and Characterization of P-PPD-Ph-Conjugated Flame Retardant

The conjugated flame retardants have rarely been studied. A conjugate flame-retardant 4, 4'-{1″, 4″-phenylene-bis [amino- (10‴-oxy10‴-hydro-9‴-hydrogen- 10‴λ⁵-phosphaphenanthrene-10″-yl)-methyl]}-diphenol (P-PPD-Ph) was synthesized and added into the polylactic acid (PLA) matrix. The P-PPD-Ph-conjugated flame-retardant structure was tested by FTIR, ¹H, and ³¹P NMR analysis. The thermal and rheological properties of PLA/P-PPD-PH-conjugated flame-retardant composites were investigated. The results showed that P-PPD-Ph-conjugated flame retardant affects PLA/P-PPD-PH-conjugated flame-retardant composites for promoting the formation of a carbon layer when the P-PPD-Ph-conjugated flame-retardant content was 15% and the residual carbon ratio for PLA/P-PPD-PH-conjugated flame-retardant composites increased by 4.2%.

Introduction

Polylactic acid (PLA) is an aliphatic polyester derived from renewable agricultural resources such as corn, rice, wheat, and sugarcane, and PLA is considered a promising material for reducing environmental pollution and solid waste disposal problems (Lin et al., 2018). PLA is widely used in medicine, construction, automotive interiors, electronic components, household goods, and transportation (Hou, et al., 2018; Jia, et al., 2018; Long, et al., 2019). As PLA is more flammable than polyethene and polypropylene, it requires flame-retardant treatment in textile, automotive, and electronic product applications (Zhang, et al., 2019; Mincheva, et al., 2020). Currently, 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) is usually added to improve the flame-retardant performance of PLA composites. DOPO is a cyclophosphamide with a diphenyl structure, which has high thermal stability, good oxidation resistance, and water resistance (Yu, et al., 2014). DOPO shows excellent flame-retardant performance in materials (Li, et al., 2019). However, the flame-retardant effect of pure DOPO added to PLA cannot meet the production needs, so many DOPO derivatives are used to improve the flame-retardant performance of composites. Yu Tao group synthesized a diacid derivative (DOPO-MA) containing maleic acid (MA) and phosphate-based compound (DOPO-ICN) containing 1, 6-hexane diisocyanate (HDI). The results showed that DOPO-MA and DOPO-ICN improved the compatibility of PLA with jute, and DOPO-MA and DOPO-ICN gave jute/PLA composites better flame-retardant performance than DOPO(Yu, et al., 2017a; Yu, et al., 2017b). Niu et al. (2020) prepared a new flame-retardant hexa-(DOPO-hydroxymethylphenoxy-dihydroxy biphenyl)-cyclotriphosphazene (HABP-DOPO) by bonding DOPO with cyclotriphosphazene. The results showed that for the PLA mixture containing 25 wt% HABP-DOPO, the LOI value reached 28.5%, and UL-94 could pass v-0. The flame retardancy of the PLA/HABP-DOPO blend was significantly improved.

In this work, a conjugated flame-retardant 4, 4'-{1″, 4″-phenylene-bis [amino- (10‴-oxy10‴-hydro-9‴-hydrogen-10‴λ⁵-phosphaphenanthrene-10″-yl)-methyl]}-diphenol (P-PPD-Ph) was synthesized. The structure of properties of P-PPD-Ph-conjugated flame retardant was investigated. Also, the combustion behavior and rheological properties of PLA/P-PPD-PH-conjugated flame-retardant composites were investigated.

Materials and Methods

Materials

9,10-Dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) was purchased from Huawei Ruike Chemical Co. Ltd. (Beijing, China); PLA (DGEBA, commercial name: E-51) was purchased from Wuxi Diaisheng Epoxy Co. Ltd. (Wuxi, China); p-phenylenediamine was purchased from Kemiou Chemical Reagent Co. Ltd. (Tianjin, China); ethanol was purchased from Tianjin Chuandong Chemical Reagent Factory (Tianjin, China); and 4-hydroxybenzaldehyde was purchased from Kemiou Chemical Reagent Co. Ltd. (Tianjin, China).

Synthesis of the Imine-Containing Compound

The imine-containing compound was synthesized according to the literature procedure (Sun and Yao, 2011). Briefly, p-phenylenediamine (0.10 mol, 10.814 g), 4-hydroxybenzalaldehyde (0.20 mol, 24.424 g), and 200 ml ethanol were added into a 500-ml round glass flask equipped with a condenser and a stirrer. The reaction mixture was stirred at 50°C under nitrogen conditions for 2 h; the reaction mixture then became thick because of the precipitation of the reaction product. Then, the mixture was cooled down to room temperature. The yellow precipitate was filtered and washed twice with ethanol and then dried at 80°C in a vacuum oven for 8 h. After drying, light yellow crystals of 31.01 g (88% yield) were obtained.

Synthesis of the P-PPD-Ph-Conjugated Flame Retardant

The P-PPD-Ph-conjugated flame retardant was synthesized according to the literature procedure (Sun and Yao, 2011). Briefly, the imine-containing compound (0.10 mol, 31.6 g) was synthesized according to 2.2, DOPO (0.20 mol, 43.237 g), and 300 ml of ethanol was added into a 500-ml round glass flask equipped with a condenser and a stirrer. The reaction mixture was stirred at 50°C for 10 h. Then, the mixture was cooled down to room temperature. The yellow precipitate was filtered and washed twice with ethanol and then dried at 80°C in a vacuum oven for 8 h. After drying, light yellow crystals of 31.61 g (88% yield) were obtained. The synthetic roadmap is shown in Figure 1A.

FIGURE 1

FIGURE 1. (A) Synthetic roadmap of P-PPD-Ph; (B) FTIR spectrum of the imine-containing compound and (C) P-PPD-Ph-conjugated flame retardant; (D) ¹H NMR spectrum of the imine-containing compound and (E) P-PPD-Ph-conjugated flame retardant; (F) ³¹P NMR spectrum of P-PPD-Ph-conjugated flame retardant; (G,H) thermal analysis of the synthesized P-PPD-Ph-conjugated flame retardant under nitrogen (N₂) atmosphere.

Preparation of PLA/P-PPD-Ph-Conjugated Flame-Retardant Composites

PLA, chain extender, and P-PPD-Ph were dried for 4 h under vacuum at 80°C before use. PLA, epoxy chain extender (4 wt‰), and P-PPD-Ph (0, 5, 10, 15 wt%) were mixed uniformly. The model of the epoxy chain extender is ADR-5481, and its structural formula is provided by the manufacturer. Then, the mixture was extruded using a twin-screw extruder (CTE 35, Coperion Keya Machinery Manufacturing Co., Ltd., China) at the temperature of 180–200°C and screw speed of 300 rpm. The extruded pellets were then molded into samples for testing with an injection molding machine (CJ80MZ2NCII, Zhende Plastic Machinery Factory, China) at 180–200°C. During the reaction, the epoxy chain extender plays the role of the “bridge” to make P-PPD-Ph react with PLA.

Characterization of the P-PPD-Ph-Conjugated Flame Retardant

The purity and structure of P-PPD-Ph-conjugated flame retardant were confirmed by FTIR, ¹H, and ³¹P NMR analysis. FTIR spectroscopy was performed using a Nicolet 6700 spectrometer (Nicolet Instrument Company, United States of America) and ¹H NMR spectrum was obtained with an Ascend 400 (Bruker BioSpin AG, Switzerland) using DMSO-d6 as a solvent with TMS as the internal standard. Also, the ³¹P NMR spectrum was obtained with an Ascend 400 (Bruker BioSpin AG, Switzerland) using DMSO-d6 as a solvent with H₃PO₄ as the internal standard.

Thermal analysis (TG) was conducted in a Q50 thermal gravimetric analyzer (TA, United States) at a heating rate of 10^°C/min and under nitrogen conditions. Approximately, 5 mg of sample was weighed and placed in an aluminium ceramic with a gas flow of 60 ml/min.

Rheological measurements were performed on an advanced rheometric expansion system (ARES, TA Instrument, United States) using the parallel plate mode. The measurements were conducted at 200 °C.

The cone calorimeter test was conducted using an FTT cone calorimeter (UK) in accordance with ISO 5660-1 standard. The specimens were prepared with sizes of 100 * 100 * 6 mm³ and tested under a heat flux of 50 kW/m². Each measurement was performed twice, and the results were averaged.

Results and Discussion

FTIR and NMR Analysis of the Imine-Containing Compound and P-PPD-Ph-Conjugated Flame Retardant and Thermal Analysis

An instrumental analysis of the powder was carried out by FTIR spectroscopy and ¹H and ³¹P nuclear magnetic resonance. Figures 1B,C show the FTIR spectrum of the imine-containing compound (FTIR absorption: C=N 1605 cm⁻¹, OH 3274 cm⁻¹) and the FTIR spectrum of the P-PPD-Ph-conjugated flame retardant (FTIR absorption: N-H stretching 3,382 cm⁻¹, O-H 3230 cm⁻¹, P-Ph 1,599 cm⁻¹, C-N 1277 cm⁻¹, P=O 1213 cm ⁻¹, and P-O 935 cm ⁻¹).

The 1H HMR spectrum of the imine-containing compound is shown in Figure 1D, δ = 6.88(H1), 6.90(H1), 7.26(H2), 7.77(H3), 7.79(H3), 8.51(H4), and 10.13(H5). Also, the ¹H HMR spectrum of P-PPD-Ph-conjugated flame retardant is shown in Figure 1E, ¹H HMR, 4.74–4.84(P-C-H′), 5.12–5.22(P-C-H), 5.46(NH′), 5.88(NH), 6.26–6.45(1, 1′), 6.67–6.73(2,2′), 7.04(11, 11′), 7.20(3,3′), 7.29(9, 9′), 7.42(10, 10′), 7.53(6,6′), 7.68–7.72(5, 5′), 8.02–8.07(7, 7′), 8.10–8.14(4, 4′ 8, 8′), 9.40(OH), and 9.44(OH’). Furthermore, P-PPD-Ph exhibits two peaks at 31.64 and 34.66 ppm in the ³¹P NMR spectrum (as Figure 1F shows), and this is because there are isomers in the P-PPD-Ph-conjugated flame-retardant structure, and this is consistent with the literature reported by Sun and Yao, (2011). The ¹H of P-PPD-Ph-conjugated flame retardant further demonstrates the presence of isomers in the P-PPD-Ph-conjugated flame-retardant structure.

The initial thermal degradation of the flame retardant occurs before the polymer decomposes, releasing the flame-retardant segment, thereby inhibiting the decomposition of the polymer matrix. The thermal degradation of P-PPD-Ph- conjugated flame retardant was investigated by TG under an N₂ atmosphere, and the results are shown in Figures 1G,H, and the corresponding data are shown in Table 1. The initial decomposition temperature (temperature after 5% decomposed) (T_−5%) of P-PPD-Ph-conjugated flame retardant was 74°C higher than the initial decomposition temperature (T_−5%) of DOPO, and the carbon residue at 800°C increased by 25.8%, which may be due to the reason that P-PPD-Ph-conjugated flame retardant contains more aromatic groups and cage effect formed by flame-retardant particles during combustion (Fina, et al., 2014), and this finding indicates that aromatic groups promote the formation of more residues for DOPO derivatives (Long, et al., 2017). But the initial decomposition temperature of P-PPD-Ph-conjugated flame retardant was lower than that of some other DOPO derivatives; this is because the thermal stability of the DOPO derivative is related to the electron density of the C atom adjacent to the P atom. The lower the electron density was, the lower the thermal stability of the carbon was, and as a result, the thermal stability of DOPO derivatives is reduced (Lin, et al., 2010). The more electronegative N atom in P-PPD-Ph-conjugated flame retardant lowers the electron density of C, so the thermal stability of P-PPD-Ph-conjugated flame retardant is lower than that of some bridged DOPO derivatives containing only P-C bonds (Wang, et al., 2017).

TABLE 1

TABLE 1. Data derived from TG analysis.

Linear Rheological Behavior of PLA/P-PPD-Ph-Conjugated Flame-Retardant Composites

Melt flow behavior for a material was usually studied by rheology, and the viscoelastic behaviors of the testing samples were investigated by rheology testing to illustrate the flame mechanism of P-PPD-Ph-conjugated flame retardant in PLA. The PLA/P-PPD-Ph-conjugated flame-retardant composites have lower storage modulus (G′), loss modulus (G″), and complex viscosity (η*) parameters than the PLA materials without flame retardants. Also, from the view of η*, the composites exhibit Newtonian-like fluid behavior, and this may be because the addition of P-PPD-Ph-conjugated flame retardant provides a larger free volume for PLA/P-PPD-Ph-conjugated flame-retardant composites, lowering the van der Waals force of the PLA, thereby reducing the complex viscosity of the PLA/P-PPD-Ph-conjugated flame-retardant composites and exhibiting shear thinning behavior. Therefore, the PLA/P-PPD-Ph-conjugated flame-retardant composites have a droplet phenomenon when burning, and the droplet takes a large amount of heat, thus obtaining a better combustion grade of the PLA/P-PPD-Ph-conjugated flame-retardant composites.

To further analyze the effect of P-PPD-Ph-conjugated flame retardant on the combustion behavior of PLA/P-PPD-Ph-conjugated flame-retardant composites, a cone calorimeter test of PLA/P-PPD-Ph-conjugated flame-retardant composites was performed. The test results are presented in Figures 2E–H; Table 2. Compared with PLA, the addition of P-PPD-Ph-conjugated flame retardant reduces TTI; this is probably because the thermal stability of P-PPD-Ph-conjugated flame retardant is relatively lower than that of PLA, and the addition of P-PPD-Ph-conjugated flame retardant reduces the thermal stability of the PLA/P-PPD-Ph-conjugated flame-retardant composites. P-PPD-Ph with 5 wt% addition has little effect on PHRR, and 10 wt% and 15wt% P-PPD-Ph reduced the PHRR values of PLA/P-PPD-Ph-conjugated flame-retardant composites by 9.1 and 16.28%, respectively, and t_p decreased with the addition of P-PPD-Ph. This further confirms that the addition of P-PPD-Ph reduces the thermal stability of the PLA-conjugated flame-retardant composites. The addition of P-PPD-Ph-conjugated flame retardant reduced the THR value, and as the amount of P-PPD-Ph-conjugated flame retardant increased, the more the THR value decreased; the THR value decreased by 14.9% when the P-PPD-Ph-conjugated flame retardant was 15 wt%. Moreover, the addition of P-PPD-Ph-conjugated flame retardant greatly increases the TSR value of the PLA/P-PPD-Ph-conjugated flame-retardant composites. In combination with Figure 2G, the CO production rate is also significantly increased due to the phosphorus-containing compounds, which the P-PPD-Ph-conjugated flame retardant releases, and these compounds can inhibit flames and thereby increase the number of components that cause incomplete combustion. EHC expresses the contribution of the active constituents of the material to the heat release in the gas phase during combustion (Qian, et al., 2015); as the amount of P-PPD-Ph-conjugated flame retardant increased, av-EHC gradually decreased, indicating that the content of effective combustion components in the gas phase component decreased. Therefore, the decrease in EHC and a significant increase in TSR and CO production suggest that the quenching activity of these compounds in PLA/P-PPD-Ph-conjugated flame-retardant composites mainly involves gaseous flame inhibition. The gas-phase flame-retardant mechanism is mainly due to the phosphorus-containing free radicals released during the decomposition of P-PPD-Ph-conjugated flame retardant, and these phosphorus-containing free radicals can capture free radicals such as H·, O·, or HO· in the flame combustion region to suppress the flame. Furthermore, PLA/P-PPD-Ph-conjugated flame-retardant composites produce more CO and less CO₂ than pure PLA during combustion. Among the compounds, with the increasing amount of P-PPD-Ph-conjugated flame retardant added, the amount of CO generated is increased, and CO₂ is reduced, and this means the addition of a flame retardant suppresses the combustion of the composites resulting in the flame-retardant effect of incomplete combustion, thus increasing the release of CO and reducing the release of CO₂ in combustion fumes and gas phase.

FIGURE 2

FIGURE 2. Storage modulus (A), loss modulus (B), complex viscosity (C), and Tan(delta) (D) vs angle frequency for the PLA/P-PPD-Ph-conjugated flame-retardant composites at 200°C and cone calorimeter test of PLA/P-PPD-Ph-conjugated flame-retardant composites; (E) HRR curves, (F) THR curves, (G) CO release curves, (H) and CO₂ release curves.

TABLE 2

TABLE 2. Cone calorimeter test data of PLA/P-PPD-Ph-conjugated flame-retardant composites.

Conclusion

The P-PPD-Ph-conjugated flame retardant was successfully synthesized by FTIR, ¹H, and ³¹P NMR analysis. The T_−5% of P-PPD-Ph-conjugated flame retardant was 74°C higher than the T_−5% of DOPO, and the carbon residue at 800°C was increased by 25.8%. The PLA/P-PPD-Ph-conjugated flame-retardant composites have lower storage modulus, loss modulus, and complex viscosity parameters. PLA/P-PPD-Ph-conjugated flame retardant affects PLA/P-PPD-Ph-conjugated flame-retardant composites for promoting the formation of the carbon layer, when the P-PPD-Ph content was 15% and the residual carbon ratio for PLA-conjugated flame-retardant composites increased by 4.2%. As the amount of flame retardant is increasingly added, the PHRR value also decreases.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material; further inquiries can be directed to the corresponding authors.

Author Contributions

JS and DZ prepared materials and carried out the experiments. KW and FT helped to analyze the experimental data. MH, DB, and SQ helped to characterize materials. DZ supervised the work. All authors contributed to revising the manuscript, approved the final version, and agreed to be accountable for all aspects of this work.

Funding

This work was supported by the Natural Science Foundation of China (grants: 51863004 and 52163001), Guizhou Province Science and Technology Projects (grants: CXTD (2021)005, GCC[2022]010-1, (2020)1Y211, and (2018)2812), Baiyun District Science and Technology Plan Projects (grants: (2019)34, (2020)28, and (2019)21), and Polymer Composites Engineering Research Center of Guizhou Minzu University (grant: GZMUGCZX (2021)01).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Fina, A., Camino, G., and Bocchini, S. (2014). Comprehensive Approach to Flame-Retardancy Evaluation of Layered Silicate Nanocomposites. Polym. Green Flame Retard., 441–459. doi:10.1016/b978-0-444-53808-6.00014-7

CrossRef Full Text | Google Scholar

Hou, Y., Liu, L., Qiu, S., Zhou, X., Gui, Z., and Hu, Y. (2018). Dopo-Modified Two-Dimensional Co-based Metal-Organic Framework: Preparation and Application for Enhancing Fire Safety of Poly(Lactic Acid). ACS Appl. Mat. Interfaces 10, 8274–8286. doi:10.1021/acsami.7b19395

PubMed Abstract | CrossRef Full Text | Google Scholar

Jia, L., Zhang, W.-C., Tong, B., and Yang, R.-J. (2018). Crystallization, Mechanical and Flame-Retardant Properties of Poly(Lactic Acid) Composites with Dopo and Dopo-Poss. Chin. J. Polym. Sci. 36, 871–879. doi:10.1007/s10118-018-2098-7

CrossRef Full Text | Google Scholar

Li, Y., Qiang, Z., Chen, X., and Ren, J. (2019). Understanding Thermal Decomposition Kinetics of Flame-Retardant Thermoset Polylactic Acid. RSC Adv. 9, 3128–3139. doi:10.1039/c8ra08770a

PubMed Abstract | CrossRef Full Text | Google Scholar

Lin, C. H., Chang, S. L., Wei, T. P., Ding, S. H., and Su, W. C. (2010). Facile, One-Pot Synthesis of Phosphinate-Substituted Bisphenol A and its Alkaline-Stable Diglycidyl Ether Derivative. Polym. Degrad. Stab. 95, 1167–1176. doi:10.1016/j.polymdegradstab.2010.04.011

CrossRef Full Text | Google Scholar

Lin, J., Zhang, W., Tong, B., and Yang, R. (2018). Crystallization, Flame-Retardant, and Mechanical Behaviors of Poly(Lactic Acid)\9,10-Dihydro-9-Oxa-10-Phosphaphenanthrene-10-Oxide-Calcium Montmorillonite Nanocomposite. J. Appl. Polym. Sci. 136, 46982–46991.

Google Scholar

Long, L., Chang, Q., He, W., Xiang, Y., Qin, S., Yin, J., et al. (2017). Effects of Bridged Dopo Derivatives on the Thermal Stability and Flame Retardant Properties of Poly(Lactic Acid). Polym. Degrad. And Stab. 139, 55–66. doi:10.1016/j.polymdegradstab.2017.03.016

CrossRef Full Text | Google Scholar

Long, L., Yin, J., He, W., Xiang, Y., Qin, S., and Yu, J. (2019). Synergistic Effect of Different Nanoparticles on Flame Retardant Poly(Lactic Acid) with Bridged Dopo Derivative. Polym. Compos. 40, 1043–1052. doi:10.1002/pc.24791

CrossRef Full Text | Google Scholar

Mincheva, R., Guemiza, H., Hidan, C., Moins, S., Coulembier, O., Dubois, P., et al. (2020). Development of Inherently Flame-Retardant Phosphorylated PLA by Combination of Ring-Opening Polymerization and Reactive Extrusion. Mater. (Basel) 13, 13–25. doi:10.3390/ma13010013

PubMed Abstract | CrossRef Full Text | Google Scholar

Niu, M., Zhang, Z., Wei, Z., and Wang, W. (2020). Effect of A Novel Flame Retardant on the Mechanical, Thermal and Combustion Properties of Poly(Lactic Acid). Polymers 12, 2407. doi:10.3390/polym12102407

PubMed Abstract | CrossRef Full Text | Google Scholar

Qian, L., Qiu, Y., Wang, J., and Xi, W. (2015). High-Performance Flame Retardancy by Char-Cage Hindering and Free Radical Quenching Effects in Epoxy Thermosets. Polymer 68, 262–269. doi:10.1016/j.polymer.2015.05.031

CrossRef Full Text | Google Scholar

Sun, D., and Yao, Y. (2011). Synthesis of Three Novel Phosphorus-Containing Flame Retardants and Their Application in Epoxy Resins. Polym. Degrad. And. Stab. 96, 1720–1724. doi:10.1016/j.polymdegradstab.2011.08.004

CrossRef Full Text | Google Scholar

Wang, Y.-Z., Yin, X.-W., Shi, Y.-Q., Wang, X.-L., Zhang, W.-Q., and Cao, Y. (2017). Bi-Dopo Structure Flame Retardants with or without Reactive Group: Their Effects on Thermal Stability and Flammability of Unsaturated Polyester. Industrial Eng. Chem. Res. 56, 5913–5924.

CrossRef Full Text | Google Scholar

Yu, T., Ding, D., Sheng, C., Tuerhongjiang, T., and Li, Y. (2017a). Enhanced Mechanical Properties and Flame Retardancy of Short Jute Fiber/Poly(Lactic Acid) Composites with Phosphorus-Based Compound. Sci. China Technol. Sci. 60, 1716–1723. doi:10.1007/s11431-016-9009-1

CrossRef Full Text | Google Scholar

Yu, T., Jiang, N., and Li, Y. (2014). Functionalized Multi-Walled Carbon Nanotube for Improving the Flame Retardancy of Ramie/Poly(Lactic Acid) Composite. Compos. Sci. Technol. 104, 26–33. doi:10.1016/j.compscitech.2014.08.021

CrossRef Full Text | Google Scholar

Yu, T., Tuerhongjiang, T., Sheng, C., and Li, Y. (2017b). Phosphorus-containing Diacid and its Application in Jute/poly(lactic Acid) Composites: Mechanical, Thermal and Flammability Properties. Compos. Part A Appl. Sci. Manuf. 97, 60–66. doi:10.1016/j.compositesa.2017.03.004

CrossRef Full Text | Google Scholar

Zhang, S., Bourbigot, S., Chen, Z., Duquesne, S., and Casetta], M. (2019). Surface Grafting of Sepiolite with A Phosphaphenanthrene Derivative and its Flame-Retardant Mechanism on PLA Nanocomposites. Polym. Degrad. Stab. 165, 68–79.

Google Scholar