Carbon nano tubes functionalized with novel functional group- amido-amine for sorption of actinides
Creators
- 1. Chemical Engineering Division, Atomic Research Centre, Trombay, Mumbai, 400085 (India)
- 2. Process Development Division, Atomic Research Centre, Trombay, Mumbai, 400085 (India)
- 3. Materials Group, Atomic Research Centre, Trombay,Mumbai, 400085 (India)
- 4. Fuel Reprocessing Division, Atomic Research Centre, Trombay, Mumbai, 400085 (India)
- 5. Waste Management Division Bhabha Atomic Research Centre, Trombay, Mumbai, 400085 (India)
Description
Highlights: • Novel amido-amine functionalized MWCNT was synthesized and characterized. • The synthesized MWCNT-AA was found to be an effective sorbent for radionuclides. • Sorption was found to be dependent on pH and ionic strength of the medium. • Sorption efficiency was found to be following the trend: U(VI) > Am(III) > Eu(III). • DFT calculations showed the reason behind the trend. - Abstract: The manuscript presents the results on the sorption of U(VI), Am(III) & Eu(III) from pH medium by a novel amido-amine functionalized multiwalled carbon nanotube (MWCNT). The novel functional group was introduced in the MWCNT by two step processes and characterized by various instrumental techniques like Scanning Electron Microscopy (SEM), Raman and X-ray Photoelectron Spectroscopy (XPS). The sorption process was found to be highly dependent on the pH of the solution with maximum sorption for both 233U, 241Am & 152+154Eu at pH 7.0. Kinetics of sorption was found to be fast with equilibrium reached in ∼15 min and the sorption was found to be following pseudo 2nd order kinetics for the radionuclides. The sorption for both 233U and 152+154Eu followed Langmuir sorption model with maximum sorption capacity of 20.66 mg/g and 16.1 mg/g respectively. This has been explained by DFT calculations which shows that more negative solvation energy of U(VI) compared to Am(III) and Eu(III) and stronger U-MWCNT-AA complex is responsible for higher sorption capacity of U(VI) compared to Am(III) and Eu(III).The synthesized amido-amine functionalized MWCNT is a very promising candidate for removal of actinides and lanthanides from waste water solution with high efficiency
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2017.11.003Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2017.11.003;
- PII
- S0304389417308257;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 345
- Journal Page Range
- p. 63-75
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 50032605
- Subject category
- S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- ACTINIDES; AMERICIUM 241; AQUEOUS SOLUTIONS; CARBON NANOTUBES; COMPUTERIZED SIMULATION; DENSITY FUNCTIONAL METHOD; EUROPIUM 152; EUROPIUM 154; RAMAN SPECTROSCOPY; RARE EARTHS; SCANNING ELECTRON MICROSCOPY; SORPTION; SYNTHESIS; URANIUM 233; WASTE WATER; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ACTINIDE NUCLEI; ALPHA DECAY RADIOISOTOPES; AMERICIUM ISOTOPES; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; CALCULATION METHODS; CARBON; DISPERSIONS; ELECTRON CAPTURE RADIOISOTOPES; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ELEMENTS; EUROPIUM ISOTOPES; EVEN-ODD NUCLEI; HEAVY ION DECAY RADIOISOTOPES; HEAVY NUCLEI; HOMOGENEOUS MIXTURES; HOURS LIVING RADIOISOTOPES; HYDROGEN COMPOUNDS; INTERMEDIATE MASS NUCLEI; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LASER SPECTROSCOPY; LIQUID WASTES; METALS; MICROSCOPY; MINUTES LIVING RADIOISOTOPES; MIXTURES; NANOSTRUCTURES; NANOTUBES; NEON 24 DECAY RADIOISOTOPES; NONMETALS; NUCLEI; ODD-EVEN NUCLEI; ODD-ODD NUCLEI; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; RADIOISOTOPES; RARE EARTH NUCLEI; SIMULATION; SOLUTIONS; SPECTROSCOPY; SPONTANEOUS FISSION RADIOISOTOPES; URANIUM ISOTOPES; VARIATIONAL METHODS; WASTES; WATER; YEARS LIVING RADIOISOTOPES
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.