Block phosphorus-containing poly(trimethylene terephthalate) copolyester via solid-state polymerization: retarded crystallization and melting behaviour

CrystEngComm ◽  
2013 ◽  
Vol 15 (14) ◽  
pp. 2688 ◽  
Author(s):  
Hong-Bing Chen ◽  
Jian-Bing Zeng ◽  
Xue Dong ◽  
Li Chen ◽  
Yu-Zhong Wang
e-Polymers ◽  
2011 ◽  
Vol 11 (1) ◽  
Author(s):  
Kim Seok Hoon ◽  
Kim Joon Ho

AbstractSolid-state polymerization has been widely used to prepare high molecular weight poly(ethylene terephthalate). Solid-state polymerization is generally carried out by heating solid, melt-phase-polymerized polymer below its melting temperature but above its glass transition temperature. Solid-state polymerization of poly(trimethylene terephthalate)(PTT) is not an independent process but rather an additional process with respect to melt polymerization that is used when PTT of a higher molecular weight is required. Two kinds of commercial PTT chips were polymerized in the solid state to prepare high molecular weight PTT, which were characterized by end group contents, molecular weight, thermal analysis and X-ray diffraction. In the solid-state polymerization of PTT, the overall reaction rate was governed by the reaction temperature, reaction time and pellet size. The content of carboxyl end groups was decreased during the solid-state polymerization with increasing reaction time and temperature. The melting temperature and crystallinity of solid-state-polymerized PTT were higher at longer times and higher temperatures of polymerization. The activation energy for the solid-state polymerization of PTT was in the range of 24~25 kcal/mol for each chip. Through the solid-state polymerization of commercial PTT chips, we could get high molecular weight polymers up to an intrinsic viscosity value of 1.63 dl/g, which is equivalent to about a 117,000 weight-average molecular weight.


2009 ◽  
Vol 009 (5) ◽  
pp. 493-498 ◽  
Author(s):  
Li CHEN ◽  
Hengzhen HUANG ◽  
Yuzhong WANG ◽  
Jinde JOW ◽  
Kenny SU

2013 ◽  
Vol 52 (15) ◽  
pp. 5326-5333 ◽  
Author(s):  
Liang-Jie Li ◽  
Rong-Tao Duan ◽  
Jun-Bo Zhang ◽  
Xiu-Li Wang ◽  
Li Chen ◽  
...  

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