The properties of the NH4-clinoptilolite .1.

被引:33
作者
Tomazovic, B
Ceranic, T
Sijaric, G
机构
[1] UNIV BELGRADE, INST PHYS CHEM, BELGRADE, YUGOSLAVIA
[2] UNIV SARAJEVO, FAC SCI, SARAJEVO 71000, BOSNIA & HERCEG
来源
ZEOLITES | 1996年 / 16卷 / 04期
关键词
high silicate clinoptilolite; ammonium-clinoptilolite; deammoniated clinoptilolite; dealuminated clinoptilolite; ion exchange; X-ray analysis; aluminum cluster;
D O I
10.1016/0144-2449(95)00118-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A clinoptilolite sample from the Zlatokop deposit (Vranje, Yugoslavia) was transformed into the mono-ionic ammonia form. Changes in the behavior of thermally treated NH4-clinoptilolite at T greater than or equal to 473 K were followed by thermal analysis (d.t.a., d.t.g., t.g.), X-ray analysis, chemical and i.r. analysis. On the basis of the results of X-ray analysis and ion exchange data, the content of clinoptilolite (about 85% w/w) and ingredients quartz and feldspars (about 15% wiw) were determined in the original sample from the deposit. Ion exchange did not affect significantly parameters of the unit cell of clinoptilolite. The prepared mono-ionic ammonia form of clinoptilolite was calcined in the temperature range 473-773 K under isothermal conditions. The structural changes in these samples were followed by X-ray analysis, which showed that the crystallinity of the calcined samples was preserved. Thermal analysis showed that the process of dehydration was developing at temperatures from 378 to 416 K, and the exothermal process of oxidation of ammonia to oxides of nitrogen at temperatures from 784 to 810 K. At T greater than or equal to 673 K the process of dealumination of clinoptilolite framework occurred too, when cationic aluminum formed different forms, depending on the temperature of calcination. By analyzing i.r. spectra of the calcined samples it was established that the degree of dealumination was the same for all samples treated at T greater than or equal to 673 K.
引用
收藏
页码:301 / 308
页数:8
相关论文
共 23 条
[1]   CRYSTAL-STRUCTURE OF 2 CLINOPTILOLITES [J].
ALBERTI, A .
TSCHERMAKS MINERALOGISCHE UND PETROGRAPHISCHE MITTEILUNGEN, 1975, 22 (01) :25-37
[2]  
ALIETTI A, 1972, AM MINERAL, V57, P1448
[3]  
Alietti A., 1977, Neues Jahrbuch fur Mineralogie-Monatshefte, V1977, P493
[4]   MOLECULAR SIEVE SORBENTS FROM CLINOPTILOLITE [J].
BARRER, RM ;
MAKKI, MB .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1964, 42 (06) :1481-&
[5]   TRANSITION-METAL ION-EXCHANGE IN ZEOLITES .2. AMMINES OF CO3+, CU2+ AND ZN2+ IN CLINOPTILOLITE, MORDENITE AND PHILLIPSITE [J].
BARRER, RM ;
TOWNSEND, RP .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1976, 72 :2650-2660
[6]   INFLUENCE OF DECATIONATION AND DEALUMINATION ON SORPTION BY MORDENITE AND CLINOPTILOLITE [J].
BARRER, RM ;
MURPHY, EVT .
JOURNAL OF THE CHEMICAL SOCIETY A -INORGANIC PHYSICAL THEORETICAL, 1970, (15) :2506-&
[7]  
BOLES JR, 1972, AM MINERAL, V57, P1463
[8]  
Ceranic T, 1987, J SERB CHEM SOC, V52, P487
[9]  
CERANIC TS, 1985, ZEOLITES, V5, P42
[10]   NATURE AND CATALYTIC ACTIVITY OF HYDROXYL-GROUPS IN CLINOPTILOLITE [J].
DETREKOY, EJ ;
JACOBS, PA ;
KALLO, D ;
UYTTERHO.JB .
JOURNAL OF CATALYSIS, 1974, 32 (03) :442-451