The market for flame retardant polymer compounds and additives

Abstract

Over the past 15 years, hyperbranched polymers have received much attention due to their unique chemical and physical properties as well as their potential applications in coatings, additives, drug and gene delivery, macromolecular building blocks, nanotechnology, and supramolecular science. Hyperbranched polymers can be prepared by means of single-monomer methodology (SMM) and double-monomer methodology (DMM). In SMM, the polymerization of an ABn or latent ABn monomer leads to hyperbranched macromolecules. SMM consists of at least four components: (1) polycondensation of ABn monomers; (2) self-condensing vinyl polymerization; (3) self-condensing ring-opening polymerization; (4) proton-transfer polymerization. In DMM, direct polymerization of two suitable monomers or a monomer pair gives rise to hyperbranched polymers. A classical example of DMM, the polymerization of A2 and Bn (n>2) monomers, is well known. Recently, a novel DMM based on the in situ formation of ABn intermediates from specific monomer pairs has been developed. This form of DMM is designated as ‘couple-monomer methodology’ (CMM) to clearly represent the method of polymerization. Many commercially available chemicals can be used as the monomers in these systems, which should extend the availability and accessibility of hyperbranched polymers with various new end groups, architectures and properties. Because a number of comprehensive reviews have been published on SMM, research involving DMM is emphasized here. In addition, recent developments in the modification, functionalization and application of hyperbranched polymers are described.