Influence of Crystal Thickness and Topological Constraints on Chain Diffusion in Linear Polyethylene
โ Scribed by Yefeng Yao; Robert Graf; HansWolfgang Spiess; Sanjay Rastogi
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 253 KB
- Volume
- 30
- Category
- Article
- ISSN
- 1022-1336
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
^13^C solidโstate exchange NMR is applied to study the influence of morphology on chain diffusion between crystalline and noncrystalline regions in ultrahigh molecular weight linear polyethylene (PE). Lamellarโdoubling reduces the exchange rate by a factor of two indicating that the chain diffusion coefficient is largely independent of the lamellar thickness. This is discussed in terms of molecular processes in the crystallites leading to chain diffusion, confirming that the role of defects is minor compared to helical jumps of extended stems. Hindrance of the chain diffusion resulting from chain entanglements was only observed after the chains diffuse over long distances. Moreover, the role of the interphase between the noncrystalline and the crystalline regions on chain diffusion is discussed.
magnified image
๐ SIMILAR VOLUMES
A strong dependence of the rotational dynamics of the mesogenic units ( brelaxation) on the order of the mesophase was found in sidechain liquid crystal polymers. The preexponential frequency factor, f \* bฯฑ , and the activation energy, E\* ab , of the b-relaxation rate both increase significantly (
tonian behavior at low shear rates with shear thinning only This paper presents diffusion studies of two ''model'' associative at relatively high shear rates. ## polymers (hydrophobically end-capped poly(ethylene oxide)) (AP) Numerous investigations with various techniques have differing in end-g
## Measurement of the kinetics of extraction of copper(II) by 19 different 5-alkyl-2-hydroxybenzaldoximes (alkyl is C 7 H 15 and C 9 H 19 ) from acidic (hydrogen sulfate buffer) aqueous solution in the range pH 3.4 -2.0, into 20% v/v toluene in n-hexane is reported. The lowering of the interfacial