Search

Six zeolite-bearing rocks, often used as building materials, were analyzed by thermodilatometry, together with a rock not bearing zeolites and a plaster covering a containing wall made of zeolite-bearing dimension stones, up to 250 °C. The main results obtained were the following: (i) the zeolite-bearing rocks exhibited very small, if any, positive variation of ΔL/Lo (%) up to about 100 °C, whereas they more or less shrank in the temperature range 100–250 °C (final values ranging from −0.21 to −0.92%), (ii) the rock not bearing zeolites regularly expanded through the whole temperature range, attaining a final value of 0.19%, (iii) the plaster showed a thermodilatometric behavior strongly affected by its water content. Obtained results were interpreted based on plain thermal expansion, shrinkage by dehydration, cation migration and thermal collapse of the zeolitic structure. The decay of the zeolite-bearing building materials was essentially related to: (i) the large differences recorded in the thermodilatometric behavior of the various rocks and the plaster, (ii) the different minerogenetic processes that resulted in the deposition of the various zeolite-bearing rocks.

Two zeolite-rich rock samples extracted from Campanian Ignimbrite tuff quarries, southern Italy, usually used as binding and anticaking agents in animal feeding, were characterized and tested in terms of their resistance in stomach, small and large intestine of pig, using a three step in vitro digestibility trial. The mineralogical composition and major and trace-elements analysis were performed after each digestion step using XRPD and ICP-OES techniques. The main zeolite phases identified are phillipsite and chabazite. Results showed that in vitro physical-chemical conditions (pH 2–3 and T 39 °C) the release of Pb and other elements from the zeolite structure is extremely low and due to the limited breakdown of the zeolite framework and glass/amorphous matter hydrolysis, by the gastric liquids. This aspect also suggests that zeolites, after the total permanence in the animal body digestive tract, can further perform their important function of cation exchanger, with also relevant relapses on the growth and health of the animal species, as well as on the environment. Moreover, the contact of zeolite material with liquids of small and large intestine leads to negligible release of undesirable elements, which are far less than those envisaged by the European Regulations.

Three Italian zeolitized volcanoclastic deposits with predominant phillipsite, chabazite or clinoptilolite were selected to investigate their attitude to form ceramized products of the Cs- and Sr-enriched forms and to evaluate the effectiveness of immobilization by means of leaching tests. The mineralogical evolution was carefully followed after thermal treatments at increasing temperatures (800 °C up to 1100 °C) which led to the crystallization of prevailing pollucite for Cs-exchanged phillipsite and chabazite and of a Sr-feldspar (about 35 wt.%) along with cristobalite and amorphous matter for all Sr-exchanged zeolites. Cs-enriched clinoptilolite at the same temperature was almost totally amorphous. Leaching tests confirm the substantial immobilization of the polluting cations in the ceramized materials with slight higher values only for the Cs-enriched clinoptilolite, mostly amorphous. Finally, calorimetric tests account for a hydrolysis process widely decreasing after thermal treatments at 1100 °C for phillipsite and chabazite, both Cs- and Sr-enriched, substantially similar for Sr-enriched clinoptilolite and definitely increased in the prevailing amorphous Cs-enriched clinoptilolite. © 2011 Elsevier B.V. All rights reserved.

Low-cost zeolitic rocks are promising substitutes for feldspathic fluxes in ceramic bodies, since their fusibility, modest hardness and high cation exchange capacity (CEC) should improve grinding and sintering. Five large-scale Italian deposits of natural zeolites with different mineralogy were characterised and tested in porcelain stoneware bodies. Their behaviour during processing was appraised and compared with that of zeolite-free bodies. Zeolites increased the slip viscosity during wet grinding, causing a coarser grain size distribution and consequently some drawbacks in both unfired and fired tiles. After overcoming this hindrance by dry grinding of zeolite rocks, the technological behaviour of zeolite-bearing tiles appear to be similar to that of current porcelain stoneware, though with larger firing shrinkage and residual closed porosity.

The aim of this research is to assess the possible use of Italian zeolitic rocks for the production of lightweight aggregates. In particular, both the expansion at high temperature and the technological features of fired products were investigated. Fifteen zeolite-bearing volcanoclastites from Northern Sardinia and three zeolitized tuffs from Campania and Tuscany (Sorano and Campanian ignimbrites and Neapolitan Yellow Tuff) were taken into account. The firing expansion turned out to be mainly dependent on the chemical composition (especially SiO 2 and fluxing oxides such as Fe 2 O 3 , Na 2 O, K 2 O, MgO and CaO) and the water content (largely related to the zeolite amount) of the raw materials. Other relevant parameters were the temperature of maximum expansion (ranging between 1350 and 1500 °C, without additives) and soaking time (between 2 and 5 min). Some products are highly impervious to water (water absorption below 1%) and exhibit a considerable firing expansion (>100% in volume), a low bulk density (0.5–0.7 g·cm −3 ) and fair technical properties (loose weight and strength of particles). These encouraging results make some of the investigated tuffs interesting raw materials for the production of lightweight aggregates.

Experiments on zeolitization were conducted on four synthetic monocationic glasses (Na, K, Ca, or Mg-rich glass) with Si/Al molar ratios of 2.67, similar in acidity to many volcanic glasses of partially zeolitized Italian tuffs. The products of the hydrothermal treatment at 100, 150, and 200°C of single glasses or glass mixtures with deionized H2O or monosaline solutions (NaCl, KCl, CaCl2) were characterized by X-ray diffraction, thermal, microscopic and chemical analyses. Chemical analyses of mother liquors were also performed. Mineral assemblages, containing chabazite, phillipsite, analcime, and K-feldspar, very similar to those found in altered, volcaniclastic alkali-trachytic or trachytic glass deposits were produced. Potassium was essential to chabazite and phillipsite crystallization, although phillipsite was obtained also in Ca-Na mixed systems. Sodium was necessary for analcime formation. Calcium plays only a secondary role in zeolitization, and magnesium does not favor zeolite crystallization but promotes the formation of smectite. Glass composition determines the mineral assemblages obtained and hence in those commonly found in nature.

A method, based on water vapour desorption, for the estimation of zeolite content in mixtures of hydrated phases is presented. The accuracy and reliability of the method and the ease of its application are demonstrated through an evaluation of the chabazite and phillipsite contents of Italian tuffs. The method is suitable for more general use provided that the pure phases of the mixture under investigation are available and their thermal features are known.