Publication result detail
THE WAY OF STEREOREGULARITY DETERMINATION OF POLYPROPYLENE
HOZA, A.; KRATOCHVÍLA, J.; HERMANOVÁ, S.
Original Title
THE WAY OF STEREOREGULARITY DETERMINATION OF POLYPROPYLENE
English Title
THE WAY OF STEREOREGULARITY DETERMINATION OF POLYPROPYLENE
Type
Peer-reviewed article not indexed in WoS or Scopus
Original Abstract
The purpose of this contribution is to evaluate and compare isotactic index determination of polypropylene homopolymer by extraction and solubility methods. A series of nine PP powder samples possessing molecular weights in the range from 29 -103 to 154-03 g/mol was investigated. Both the methods afforded fractionation of polypropylene into two portions, the soluble fraction and the insoluble one. Extractions were carried out in a modified Kumagawa extractor. Solvent extracts were obtained from polypropylene powders using several organic solvents (n-pentane, n-hexane, n-heptane, and n-octane) at their boiling points. Soluble fractions were prepared by dissolving polypropylene powder in high boiling solvents (xylene, decahydronaphthalene, and 1,2,3,4-tetrahydronaphthalene) and cooling polymer solutions to 23 degree C. All the fractions were characterized using 13C-NMR, DSC, and SEC methods. Comparison of extraction and solubility methods showed a significant differences in the amount, structure, molecular weight, and crystalinity of soluble and insoluble fractions
English abstract
The purpose of this contribution is to evaluate and compare isotactic index determination of polypropylene homopolymer by extraction and solubility methods. A series of nine PP powder samples possessing molecular weights in the range from 29 -103 to 154-03 g/mol was investigated. Both the methods afforded fractionation of polypropylene into two portions, the soluble fraction and the insoluble one. Extractions were carried out in a modified Kumagawa extractor. Solvent extracts were obtained from polypropylene powders using several organic solvents (n-pentane, n-hexane, n-heptane, and n-octane) at their boiling points. Soluble fractions were prepared by dissolving polypropylene powder in high boiling solvents (xylene, decahydronaphthalene, and 1,2,3,4-tetrahydronaphthalene) and cooling polymer solutions to 23 degree C. All the fractions were characterized using 13C-NMR, DSC, and SEC methods. Comparison of extraction and solubility methods showed a significant differences in the amount, structure, molecular weight, and crystalinity of soluble and insoluble fractions
Keywords
Isotactic index, polypropylene, extraction
Key words in English
Isotactic index, polypropylene, extraction
Authors
HOZA, A.; KRATOCHVÍLA, J.; HERMANOVÁ, S.
RIV year
2010
Released
09.09.2008
ISBN
1213-7103
Periodical
CHEMICKE LISTY
Volume
102
Number
15
State
Czech Republic
Pages from
s1202
Pages to
s1206
Pages count
5