Startseite Modified synthesis scheme for N,N´-dimethyl-N,N´-dioctyl-2,(2´-hexyloxyethyl) malonamide (DMDOHEMA) and its comparison with proposed solvents for actinide partitioning
Artikel
Lizenziert
Nicht lizenziert Erfordert eine Authentifizierung

Modified synthesis scheme for N,N´-dimethyl-N,N´-dioctyl-2,(2´-hexyloxyethyl) malonamide (DMDOHEMA) and its comparison with proposed solvents for actinide partitioning

  • Ajay B. Patil , Vaishali S. Shinde , P. N. Pathak , P. K. Mohapatra und V. K. Manchanda
Veröffentlicht/Copyright: 6. November 2012

Abstract

N,N´-dimethyl-N,N´-dioctyl-2,(2´-hexyloxyethyl) malonamide (DMDOHEMA) has been synthesized by a relatively simpler route with a better yield than the conventional procedures for the synthesis of pentaalkyl substituted diamides. The proposed route replaces the use of acid chlorides and brominating agents (corrosive in nature) by acid diester and p-toluene sulphonyl (tosyl) chloride, respectively. The later easily replaces hydrogen from primary OH group of the 3-oxanonyl side chain and relatively less corrosive. The synthesized product has been tested for the extraction behavior of 241Am, Np, Pu as pure tracers as well as under Pressurized Heavy Water Reactor (PHWR) Simulated High-Level Waste (SHLW) conditions. The stoichiometries of extracted species of Np(IV), Pu(IV), and Am(III) from 3 M HNO3 using varying concentrations of DMDOHEMA in n-dodecane has been determined. The effect of the nature of mineral acid (viz. HCl, HNO3, and HClO4) on the extraction of Am(III) has also been investigated employing DMDOHEMA and N,N´-dimethyl-N,N´-dibutyl-tetradecyl malonamide (DMDBTDMA) as extractants and explained in terms of the aggregation behavior of diamides. The performance of DMDOHEMA has been evaluated vis-à-vis other proposed extractants for actinide partitioning under PHWR-SHLW conditions.


* Correspondence address: Bhabha Atomic Research Centre, Radiochemistry Division, 400085 Trombay, Mumbai, Indien,

Published Online: 2012-11-06
Published in Print: 2013-02

© by Oldenbourg Wissenschaftsverlag, München, Germany

Heruntergeladen am 28.11.2025 von https://www.degruyterbrill.com/document/doi/10.1524/ract.2013.1998/pdf?lang=de
Button zum nach oben scrollen