Handbook of Polymer Synthesis, Characterization, and Processing 2013
DOI: 10.1002/9781118480793.ch3
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Step‐Growth Polymerization

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Cited by 8 publications
(8 citation statements)
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“…Furthermore, an extended reaction time from 5 to 12 h effectively promoted the polymerization with a high M n of 18.9 kDa, suggesting the step-growth characteristics of these polymerizations. 10 As such, further extending the reaction time could still improve the M n , but slightly (Table 1, entries 4–6). Considering the polymerization results and time cost, we adopted 12 h as the reaction time for further research.…”
Section: Resultsmentioning
confidence: 96%
“…Furthermore, an extended reaction time from 5 to 12 h effectively promoted the polymerization with a high M n of 18.9 kDa, suggesting the step-growth characteristics of these polymerizations. 10 As such, further extending the reaction time could still improve the M n , but slightly (Table 1, entries 4–6). Considering the polymerization results and time cost, we adopted 12 h as the reaction time for further research.…”
Section: Resultsmentioning
confidence: 96%
“…This means that the equilibrium constants for processes of the same type can be considered identical. It is believed that polymers are present in the equilibrium state according to the polymerization degree from 1 to ∞ [3,8]. Equation 1only roughly conveys the composition of the products, because condensation telomerization, as a polycondensation process, proceeds statistically [3,7].…”
Section: Resultsmentioning
confidence: 99%
“…It is believed that polymers are present in the equilibrium state according to the polymerization degree from 1 to ∞ [3,8]. Equation 1only roughly conveys the composition of the products, because condensation telomerization, as a polycondensation process, proceeds statistically [3,7]. If to consider the interaction of only monomer substances, it is possible to distinguish the following basic linearly independent reactions: In (2) the equilibrium constants K 1 and K 2 are associated, respectively, with the processes of growth and chain termination.…”
Section: Resultsmentioning
confidence: 99%
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“…2 Common methods for the synthesis of PEs include the step-growth polymerization of hydroxy acids or diol/diacid pairs, and the ring-opening polymerization (ROP) of lactones. 3 Among bio-based PEs, 4 polyfuranoates are of particular interest as sustainable alternatives to industrial PEs derived from terephthalic acid such as poly(ethylene terephthalate) (PET) and poly(butylene terephthalate) (PBT). 5 Indeed, poly(ethylene furanoate) (PEF) and poly(butylene furanoate) (PBF) are going to be produced on a large scale due to their favorable mechanical and barrier properties, recyclability, and integration within the context of a circular economy.…”
Section: Introductionmentioning
confidence: 99%