z-logo
open-access-imgOpen Access
“Pseudo solid” nuclear spin echo study of poly(ethylene oxide) grafted on silica. Comparison with magic‐angle spinning technique results
Author(s) -
Tajouri Tahar,
Ben Mariem Mohamed Aymen,
Hommel Hubert
Publication year - 2015
Publication title -
concepts in magnetic resonance part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.229
H-Index - 49
eISSN - 1552-5023
pISSN - 1546-6086
DOI - 10.1002/cmr.a.21365
Subject(s) - spinning , magic angle spinning , ethylene oxide , materials science , ethylene , poly ethylene , magic angle , nuclear magnetic resonance , polymer chemistry , chemistry , physics , nuclear magnetic resonance spectroscopy , composite material , organic chemistry , copolymer , catalysis , polymer
Abstract The polymer/solid interface of Poly (ethylene oxide) ( PEO ) grafted on silica is studied by 1 H NMR . For grafted polymers, the dipolar interaction is an important factor in the spin–spin relaxation process. For this purpose, the part of the dipolar interaction that is not averaged to zero by the motion is used. The “pseudo solid” spin echo can indeed give an estimation of the nonzero average dipolar interactions. The appropriate pulse sequence permits a standard measurement of the average dipolar spin coupling involved in the transverse magnetization relaxation. The influence of some major parameters such as molecular weights of the chains, grafting ratios, and temperatures on the relaxation and ultimately on the concentration is followed by “pseudo solid” spin echo. The magic‐angle spinning technique is also used. The sample rotation confirms by the narrowing of the central line and the appearance of side bands, the existence of a residual dipolar interaction which reveals the concentration of high monomer units at the surface. The study of the side bands permits to calculate the second moment as a function of temperature. A fair agreement is obtained by these two independent techniques: pseudo solid echo and magic‐angle spinning.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here