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Chain-growth polymerization or chain-growth polymerisation is a polymerization technique where monomer molecules add onto the active site on a growing polymer chain one at a time. [1] There are a limited number of these active sites at any moment during the polymerization which gives this method its key characteristics.
In chain-growth (or chain) polymerization, the only chain-extension reaction step is the addition of a monomer to a growing chain with an active center such as a free radical, cation, or anion. Once the growth of a chain is initiated by formation of an active center, chain propagation is usually rapid by addition of a sequence of monomers.
Living polymerization: A chain polymerization from which chain transfer and chain termination are absent. Note : In many cases, the rate of chain initiation is fast compared with the rate of chain propagation, so that the number of kinetic-chain carriers is essentially constant throughout the polymerization.
Step-growth polymerization can be divided into polycondensation, in which low-molar-mass by-product is formed in every reaction step, and polyaddition. Example of chain polymerization: Radical polymerization of styrene, R. is initiating radical, P. is another polymer chain radical terminating the formed chain by radical recombination.
In polymer chemistry, ring-opening metathesis polymerization (ROMP) is a type of chain-growth polymerization involving olefin metathesis. [1] The reaction is driven by relieving ring strain in cyclic olefins. [2] A variety of heterogeneous and homogeneous catalysts have been developed for different polymers and mechanisms. [3]
RAFT polymerization today is mainly carried out by thiocarbonylthio chain transfer agents. It was first reported by Rizzardo et al. in 1998. [6] RAFT is one of the most versatile methods of controlled radical polymerization because it is tolerant of a very wide range of functionality in the monomer and solvent, including aqueous solutions. [7]
Chain-growth supramolecular polymerization in a broad sense involves two distinct phases; a less favored nucleation and a favored propagation. In this mechanism, after the formation of a nucleus of a certain size, the association constant is increased, and further monomer addition becomes more favored, at which point the polymer growth is ...
Flory postulated that his treatment can also be applied to chain-growth polymerization mechanisms, as the three criteria stated above are satisfied under the assumptions that (1) the probability of chain termination is independent of chain length, and (2) multifunctional co-monomers react randomly with growing polymer chains. [1]