Influence of the Solvent on the Formation of CNR/BNR Polymer Blends


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

Structural dynamic analysis combining IR spectroscopy, DSC, and EPR spectroscopy is applied to studying films based on chlorinated natural rubber (CNR), butadiene nitrile rubber (BNR), and blends thereof. The influence of various solvents, such as methyl ethyl ketone (MEK), ethyl acetate (EA), methyl acetate (MA), and acetone (A), on the structure and molecular dynamics (τ) of CNR/BNR polymer films is examined. The strongest changes in the molecular mobility (τ) and the glass transition temperature (Tgt) relative to those of the starting materials are observed for the 50: 50% CNR/BNR blends prepared using all the solvents (except for acetone, the maximum values of τ for which is observed at a ratio of CNR: BNR = 80: 20%), which can be explained by the inversion of phases in the blends. Annealing at 140°С causes an increase in the correlation time of the probe, and, consequently, a decrease in the molecular mobility, which is due to the intermolecular crosslinking of the components.

About the authors

S. G. Karpova

Emanuel Institute of Biochemical Physics

Author for correspondence.
Email: karpova@sky.chph.ras.ru
Russian Federation, Moscow, 119991

E. G. Milyushkina

Moscow Technological University (Institute of Fine Chemical Technologies)

Email: karpova@sky.chph.ras.ru
Russian Federation, Moscow, 119571

L. R. Lusova

Moscow Technological University (Institute of Fine Chemical Technologies)

Email: karpova@sky.chph.ras.ru
Russian Federation, Moscow, 119571

Yu. A. Naumova

Moscow Technological University (Institute of Fine Chemical Technologies)

Email: karpova@sky.chph.ras.ru
Russian Federation, Moscow, 119571

A. A. Popov

Plekhanov Russian Economic University

Email: karpova@sky.chph.ras.ru
Russian Federation, Moscow, 117997

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2018 Pleiades Publishing, Ltd.