Chemical Upcycling of Nitrile Butadiene Rubbers to Polyamines and Polyols by Chemoselective Catalytic Hydrogenation

A Alejandra Sophia Lozano Perez (EaStCHEM, School of Chemistry University of St Andrews St Andrews UK) R Raymundo Marcial‐Hernandez (EaStCHEM, School of Chemistry University of St Andrews St Andrews UK) H Harini Sampathkumar (School of Computing, Engineering and Technology, The Sir Ian Wood Building Robert Gordon University Aberdeen UK) O Oluchi Emenike (School of Computing, Engineering and Technology, The Sir Ian Wood Building Robert Gordon University Aberdeen UK) K Ketan Pancholi C Claire N. Brodie (EaStCHEM, School of Chemistry University of St Andrews St Andrews UK) D Daniel M. Dawson (EaStCHEM, School of Chemistry University of St Andrews St Andrews UK) A Amit Kumar

Abstract

ABSTRACT We report here two new approaches for the chemical recycling/upcycling of nitrile butadiene rubber (NBR) to make either polyamines or polyols. Both processes are achieved through ruthenium‐catalyzed hydrogenation reactions, where the chemoselective reduction of nitriles leads to the formation of either amines or alcohols. The hydrogenation of NBR to polyamines could be achieved at temperatures as low as 35°C, whereas a higher temperature (150°C) was required for the formation of polyols with catalytic turnover numbers reaching up to 2000. Additionally, polyamines were demonstrated for their potential application in CO 2 capture, absorbing 1.34 mmol of CO 2 /g of absorbents. This was significantly higher in comparison to that obtained in the case of NBR, which absorbed only 0.015 mmol of CO 2 /g of absorbent. The synthesized polyol exhibited a markedly greater ductility than the commercial NBR, reaching an elongation at break of ≈ 550% versus ≈ 420% for NBR, suggestive of potential use in stretch‐demanding applications.

Article Details

Volume / Issue Vol. 65, Issue 18
Published April 27, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

A

Alejandra Sophia Lozano Perez

EaStCHEM, School of Chemistry University of St Andrews St Andrews UK

R

Raymundo Marcial‐Hernandez

EaStCHEM, School of Chemistry University of St Andrews St Andrews UK

H

Harini Sampathkumar

School of Computing, Engineering and Technology, The Sir Ian Wood Building Robert Gordon University Aberdeen UK

O

Oluchi Emenike

School of Computing, Engineering and Technology, The Sir Ian Wood Building Robert Gordon University Aberdeen UK

K

Ketan Pancholi

C

Claire N. Brodie

EaStCHEM, School of Chemistry University of St Andrews St Andrews UK

D

Daniel M. Dawson

EaStCHEM, School of Chemistry University of St Andrews St Andrews UK

A

Amit Kumar