M. H. Al-Majidi, S. (2007). Synthesis of Poly [Allylamine-Co-Butadiene] form reduction of Poly [Acrylonitrile-Co-Butadiene] and grafting the product with Amic acids. , 48(1), 1-6.
Suaad M. H. Al-Majidi. "Synthesis of Poly [Allylamine-Co-Butadiene] form reduction of Poly [Acrylonitrile-Co-Butadiene] and grafting the product with Amic acids". , 48, 1, 2007, 1-6.
M. H. Al-Majidi, S. (2007). 'Synthesis of Poly [Allylamine-Co-Butadiene] form reduction of Poly [Acrylonitrile-Co-Butadiene] and grafting the product with Amic acids', , 48(1), pp. 1-6.
M. H. Al-Majidi, S. Synthesis of Poly [Allylamine-Co-Butadiene] form reduction of Poly [Acrylonitrile-Co-Butadiene] and grafting the product with Amic acids. , 2007; 48(1): 1-6.

Synthesis of Poly [Allylamine-Co-Butadiene] form reduction of Poly [Acrylonitrile-Co-Butadiene] and grafting the product with Amic acids

Iraqi Journal of Science
Article 1, Volume 48, Issue 1, 2007, Pages 1-6
Author
Suaad M. H. Al-Majidi
Abstract
Pure Poly [Allylamine-Co-Butadiene] having high molecular weight was prepared for the first time from the reduction of the Poly [Acrylonitrile-Co-Butadiene] using Lithium Aluminium hydride. Softening point of the prepared polymer was (201-207)C, conversion percent was 88%, with intrinsic viscosity of the new polymer in benzene as a solvent was 1.56.
Then the new polymer was allowed to react with six acid anhydrides, (Maleic, Phthalic, Succinic, Glutaric, 1,8-Naphthalic and cis 1,2,3,4-tetrahydrophthalic) to produce six novel pendant polymers which contain the acids reffered above in its recurrent units. The prepared poly [N-(ally)substituted amic acid-Co-butadiene] polymers were characterized using FTIR, H-NMR, and some specific tests.
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