Green Synthesis of Organic Fire Retardants

Author:

Liu Yuan1,Xu Miaojun2,Feng Jiabing3,Song Pingan45,Yang Hongyu6

Affiliation:

1. aPolymer Research Institute, Sichuan University, China

2. bHeilongjiang Key Laboratory of Molecular Design and Preparation of Flame Retarded Materials, College of Chemistry, Chemical Engineering and Resource Utilization, Northeast Forestry University, Harbin 150040, People’s Republic of China

3. cChina-Australia Institute for Advanced Materials and Manufacturing, Jiaxing University, Jiaxing 314001, China

4. dSchool of Agriculture and Environmental Science, University of Southern Queensland, Springfield 4300, Australia

5. eCentre for Future Materials, University of Southern Queensland, Springfield 4300, Australia

6. fCollege of Materials Science and Engineering, Chongqing University, Chongqing, 400044, China

Abstract

Traditional synthetic methods of organic fire retardants include the dehydrochlorination reaction, ring-opening reaction, Mannich reaction, etc., which are often carried out in a large volume of toxic solvents (e.g., acetonitrile, dichloromethane, and triethylamine), and would lead to industrial waste and even threaten our environment without proper treatment. The post-treatment processes are also complex. For this reason, some efforts have been made to develop a green approach (e.g., solventless, self-assembly, etc.) for their synthesis. Aiming at the sustainable development of fire retardants, this chapter focuses on four representatives of organic fire retardants, including melamine cyanurate (MCA), triazine-based charring agents, (poly)phosphoramides, and covalent organic frameworks (COFs), providing a thorough summary of their green synthesis mechanisms, research progress, and production processes.

Publisher

Royal Society of Chemistry

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