A series of N-alkyl-p-toluenesulfonamides (ATSA) were synthesized and identified. The measurement of solution viscosity of poly(ethy1ene terephthalate) (PET) proved that ATSA does not react with PET during the melting process of PET/ATSA mixtures, and consequently does not cause any decrease of mole
Activity of substrates in the catalyzed nucleation of poly(ethylene terephthalate) melts
β Scribed by A. Dobreva; M. Alonso; M. Gonzalez; J. A. De Saja
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 164 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
The activity, F, of AgBr, AgI, PbF 2 , Ag 2 S, LiF, and CaF 2 in the catalyzed nucleation of poly(ethylene terephthalate) (PET) melts was determined using a nonisothermal differential scanning calorimetry (DSC) technique. A comparison with existing experimental data was made. It is established that the higher the melting temperature of the substrate the lower its activity as a crystallization core in the heterogeneous nucleation of PET. The lateral surface energy, s, the end surface energy, s e , the adhesion energy, b, and the difference between the surface energies at the substrate/melt, s s f , substrate/deposit, s*, and the total energy of misfit dislocations, E d [i.e., s s f 0 (s* 0 E d )] were calculated.
π SIMILAR VOLUMES
A modified mathematical model based on the melting and recrystallization of an initial distribution of melting temperatures satisfactorily predicts the melting behavior of PET in differential scanning calorimetry. The simulated DSC curves produced in this work agreed fairly well not only with experi
The necking behavior in the high-speed melt-spinning process of poly(ethylene terephthalate) (PET) was analyzed using a mathematical simulation under a nonisothermal condition. A constitutive model into which the strain-rate dependence of viscosity and the strain-hardening effect are incorporated wa