2002
DOI: 10.1016/s0032-3861(02)00680-8
|View full text |Cite
|
Sign up to set email alerts
|

Degree of comonomer inclusion into lamella crystal for propylene/olefin copolymers

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

8
122
2

Year Published

2004
2004
2017
2017

Publication Types

Select...
5
5

Relationship

0
10

Authors

Journals

citations
Cited by 83 publications
(132 citation statements)
references
References 37 publications
8
122
2
Order By: Relevance
“…It has been observed that the methyl and, to a lesser extent, ethyl branches can be included in the crystallites, due to their small sizes, while propyl and longer branches are completely excluded. [5][6][7][8] Using solid state NMR, White and co-workers 9 also reported an increase in the interfacial content (i.e. "constrained amorphous" plus "mobile all-trans" fractions) with increasing co-monomer content.…”
Section: Introductionmentioning
confidence: 98%
“…It has been observed that the methyl and, to a lesser extent, ethyl branches can be included in the crystallites, due to their small sizes, while propyl and longer branches are completely excluded. [5][6][7][8] Using solid state NMR, White and co-workers 9 also reported an increase in the interfacial content (i.e. "constrained amorphous" plus "mobile all-trans" fractions) with increasing co-monomer content.…”
Section: Introductionmentioning
confidence: 98%
“…[35][36][37][38][39][40] Ethylene comonomer, due to its small size, is not excluded from the crystal lattice, but it interrupts the iPP helix, shortening the crystal sequence and incorporating these distorted sequences to the amorphous fraction of the polymer. [37,41,42] Figure 1a also shows the totally amorphous profile, amPP, of an elastomeric PP sample [30] , in this case scaled to account for the amorphous component corresponding to the terpolymer. By subtraction of this amorphous component (adequately scaled for each sample), the pure crystalline profiles (shown in figure 1b) can be obtained, as well as the overall X-ray degree of crystallinity, f cTOTAL .…”
Section: Experimental Partmentioning
confidence: 99%
“…However, if the chain length of the comonomer is closer to the main monomer, the impact would become weak. The change of the melting temperature of the propylene copolymer with 1-butene [36], 1-hexene [37,38], 1-octene [37] and 1-decene [37] showed that, the incorporation of the shorter comonomer would be less efficient to decrease the melting temperature of the copolymer. Previous research revealed that 1-butene was more inclined to be incorporated into the crystalline phase than ethylene, 1-hexene and 1-octene for propylene copolymers [39].…”
Section: Thementioning
confidence: 99%