Thermal transformations of (NH4, Cs)-clinoptilolite with compositions in between the end-members

被引:8
作者
Cerri, Guido [1 ]
Sale, Eleonora [1 ]
Brundu, Antonio [1 ]
机构
[1] Sassari Univ, Dept Nat & Terr Sci, Via Piandanna 4, I-07100 Sassari, Italy
关键词
CsAlSi5O12; Mullite; Pollucite; Ammonium; Zeolite; SYSTEM CS2O-AL2O3-SIO2; ZEOLITE-A; CLINOPTILOLITE; CESIUM; CS; ALUMINOSILICATE; TEMPERATURE; STABILITY; MULLITE; PHASE;
D O I
10.1016/j.micromeso.2017.09.008
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A powder containing about 90% of clinoptilolite in ammonium form, previously employed in a study concerning the thermal transformations of NH4-clinoptilolite, was used to prepare three samples with the following Cs+/NH4+ ratios: 0.51; 1.16; 5.00. These samples were subjected to thermal treatments of 2 h up to 1200 degrees C. Further treatments were executed at 1100 degrees C for 4, 8, 16 and 32 h. (NH4, Cs)-clinoptilolite underwent dehydration, de-ammoniation, dehydroxylation followed by amorphization and crystallization of new phases. Amorphization temperature increased, from 800 to 1000 degrees C, with the increase of cesium content. The composition of extraframework cations played the main role in determining the type and quantity of phases in the final products, as well as the kinetics of the crystallization. Basically, the thermal transformation of (NH4, Cs)-clinoptilolite can be described by two reactions producing: i) CsAlSi5O12 (CAS) + pollucite + glass, occurred in all samples; ii) mullite + cristobalite/tridymite + glass, occurred when Cs+/NH4+ <= 1.16. All samples showed the lowest residual glass content after 32 h at 1100 degrees C. The treatment of (NH4, Cs)-clinoptilolite with Cs+/NH4+ >= 1.16 allowed to confine all the cesium in crystalline phases, and the residual glass was below 15%. Conversely, when Cs+/NH4+ = 0.51 most of the cesium was in the prevalent (approximate to 60%) amorphous phase. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:122 / 130
页数:9
相关论文
共 54 条
[1]   CSALSI5O12 - A POSSIBLE HOST FOR CS-137 IMMOBILIZATION [J].
ADL, T ;
VANCE, ER .
JOURNAL OF MATERIALS SCIENCE, 1982, 17 (03) :849-855
[2]   Reconstructive phase transitions in microporous materials: Rules and factors affecting them [J].
Alberti, Alberto ;
Martucci, Annalisa .
MICROPOROUS AND MESOPOROUS MATERIALS, 2011, 141 (1-3) :192-198
[3]  
Alietti A., 1974, Mineral. Petrol, V21, P291
[4]  
[Anonymous], REND ONLINE SOC GEOL
[5]  
[Anonymous], IND MINERALS ROCKS C
[6]   CRYSTAL-STRUCTURE OF A CESIUM ALUMINOSILICATE, CS[ALSI5O12] [J].
ARAKI, T .
ZEITSCHRIFT FUR KRISTALLOGRAPHIE, 1980, 152 (3-4) :207-213
[7]  
Armbruster T., 2001, Zeolites and mesoporous materials at the dawn o f the 21st century. Studies in Surface Science and Catalysis, V135, P13, DOI [10.1016/s0167-2991, DOI 10.1016/S0167-2991, DOI 10.1016/S0167-2991(01)81183-6, 10.1016/S0167-2991(01)81183-6]
[8]   Clinoptilolite-heulandite nomenclature [J].
Bish, DL ;
Boak, JM .
NATURAL ZEOLITES: OCCURRENCE, PROPERTIES, APPLICATIONS, 2001, 45 :207-216
[9]   Examining the Nuclear Accident at Fukushima Daiichi [J].
Blandford, Edward D. ;
Ahn, Joonhong .
ELEMENTS, 2012, 8 (03) :189-194
[10]   Safe trapping of Cs in heat-treated zeolite matrices [J].
Bosch, P ;
Caputo, D ;
Liguori, B ;
Colella, C .
JOURNAL OF NUCLEAR MATERIALS, 2004, 324 (2-3) :183-188