A New Approach to Reducing the Flammability of Layered Double Hydroxide (LDH)-Based Polymer Composites: Preparation and Characterization of Dye Structure-Intercalated LDH and Its Effect on the Flammability of Polypropylene-Grafted Maleic Anhydride/d-LDH Composites

被引:102
作者
Kang, Nian-Jun [1 ]
Wang, De-Yi [1 ]
Kutlu, Burak [2 ,3 ]
Zhao, Peng-Cheng [3 ]
Leuteritz, Andreas [2 ]
Wagenknecht, Udo [2 ]
Heinrich, Gert [2 ,3 ]
机构
[1] Madrid Inst Adv Studies Mat IMDEA Mat, Madrid 28906, Spain
[2] Leibniz Inst Polymerforsch Dresden eV, D-01069 Dresden, Germany
[3] Tech Univ Dresden, Inst Werkstoffwissensch, D-01069 Dresden, Germany
关键词
layered double hydroxide (LDH); flammability; polymer composites; dye structure; polypropylene-grafted maleic anhydride; heat release rate; THERMAL-PROPERTIES; AMINO-ACIDS; NANOCOMPOSITES; POLYPHOSPHATE; BEHAVIORS;
D O I
10.1021/am4020555
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Dye structure-intercalated layered double hydroxide (d-LDH) was synthesized using a one-step method, and its intercalated behaviors have been characterized by Fourier transform infrared spectroscopy (FTIR), wide angle X-ray scattering (WAXS), scanning electron microscopy, thermogravimetric analysis (TGA), etc. As a novel functional potential fire-retarding nanofiller, it was used to prepare a polypropylene-grafted maleic anhydride (PP-g-MA)/d-LDH composite by refluxing the mixture of d-LDH and PP-g-MA in xylene, aiming to investigate its effect on the flammability of the PP-g-MA composite. The morphological properties, thermal stability, and flame retardant properties of the PP-g-MA/d-LDH composite were determined by FTIR, WAXS, transmission electron microscopy, TGA, and microscale combustion calorimetry. Compared with NO3-LDH (unmodified LDH) and LDH intercalated by sodium dodecylbenzenesulfonate (conventional modified LDH), d-LDH can significantly decrease the heat release rate and the total heat release of the PP-g-MA composite, offering a new approach to imparting low flammability to LDH-based polymer composites.
引用
收藏
页码:8991 / 8997
页数:7
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