Temperature programmed decomposition of uranyl nitrate hexahydrate

被引：34

作者：

Dash, S

Kamruddin, M

Bera, S

Ajikumar, PK

Tyagi, AK

Narasimhan, SV

Raj, B ^{[1
]}

机构：

[1] Indira Gandhi Ctr Atom Res, Met & Mat Grp, Kalpakkam 603102, Tamil Nadu, India

[2] Water & Steam Chem Lab, BARC Facilit, Kalpakkam 603102, Tamil Nadu, India

来源：

JOURNAL OF NUCLEAR MATERIALS | 1999年 / 264卷 / 03期

关键词：

D O I：

10.1016/S0022-3115(98)00495-4

中图分类号：

T [工业技术];

学科分类号：

08 ;

摘要：

Temperature programmed decomposition (TPD) of uranyl nitrate hexahydrate has been studied using evolved gas analysis mass spectrometry (EGA-MS) in the temperature range 300-1400 K. Thermogravimetric (TGA) investigations were performed in the temperature range 300-1100 K. An attempt has been made to resolve the complexity of decomposition behaviour through suitable comparison of TcA and EGA-MS data. Kinetic control regimes for various decomposition stages could be deduced from EGA-MS data. The corresponding activation energies and frequency factors were also evaluated. Kinetics based on random nucleation and diffusion was found to be rate controlling. The residue left over after each decomposition stage was analysed by XRD and XPS to determine structure and composition. The ultimate product was found to be a mixture of UO3H1.17 and U3O8: the former being a topotactic hydrogen spill over compound of UO3. Complete conversion of this residue to U3O8 was noticed during ion beam exposure of the residue which was performed in the course of XPS investigations. (C) 1999 Elsevier Science B.V. All rights reserved.

引用

页码：271 / 282

页数：12

共 51 条

[1]

ALNGER HG, 1983, TREATISE ANAL CHEM 1, V12

[2]

BABER M, 1973, ADV NUCL SCI TECHNOL, V7

[3]

BALL MC, 1974, J INORG NUCL CHEM, V6, P1577

[4] CRYSTAL STRUCTURE AND ANISOTROPIC THERMAL EXPANSION OF BETA-URANYL DIHYDROXIDE, UO2(OH)2 [J].