The crystal structure of the killer fibre erionite from Tuzköy (Cappadocia, Turkey).

Erionite is a non-asbestos fibrous zeolite classified by the International Agency for Research on Cancer (IARC) as a Group 1 carcinogen and is considered today similar to or even more carcinogenic than the six regulated asbestos minerals. Exposure to fibrous erionite has been unequivocally linked to cases of malignant mesothelioma (MM) and this killer fibre is assumed to be directly responsible for more than 50% of all deaths in the population of the villages of Karain and Tuzköy in central Anatolia (Turkey). Erionite usually occurs in bundles of thin fibres and very rarely as single acicular or needle-like fibres. For this reason, a crystal structure of this fibre has not been attempted to date although an accurate characterization of its crystal structure is of paramount importance for our understanding of the toxicity and carcinogenicity. In this work, we report on a combined approach of microscopic (SEM, TEM, electron diffraction), spectroscopic (micro-Raman) and chemical techniques with synchrotron nano-single-crystal diffraction that allowed us to obtain the first reliable ab initio crystal structure of this killer zeolite. The refined structure showed regular T-O distances (in the range 1.61-1.65 Å) and extra-framework content in line with the chemical formula (K2.63Ca1.57Mg0.76Na0.13Ba0.01)[Si28.62Al7.35]O72·28.3H2O. The synchrotron nano-diffraction data combined with three-dimensional electron diffraction (3DED) allowed us to unequivocally rule out the presence of offretite. These results are of paramount importance for understanding the mechanisms by which erionite induces toxic damage and for confirming the physical similarities with asbestos fibres.

Natural Zeolite for The Purification of Saline Groundwater and Irrigation Potential Analysis.

Groundwater is one of the main sources of water for irrigation used worldwide. However, the application of the resource is threatened by the possibility of high saline levels, especially in low-lying coastal regions. Furthermore, the lack of readily accessible materials for successful treatment procedures makes the purification of such water a constant challenge. Based on the fact that natural zeolite is one of the easily accessible and relatively cheap filter materials, this study examined the potential use of high-salinity groundwater filtered by natural zeolite for irrigation. Zeolite-filled filters at two different depths (0.5 m and 1 m) were studied. The samples were collected from the low-lying areas of Dar es Salaam City, Tanzania. The study observed that when the raw groundwater samples were exposed to the 0.5 m column depth, sodium (Na+) had the lowest removal efficiency at 40.2% and calcium (Ca2+) had the highest removal efficiency at 98.9%. On the other hand, magnesium (Mg2+) had the lowest removal efficiency, at about 61.2%, whereas potassium (K+) had up to about 99.7% removal efficiency from the 1 m column depth treatment system. Additionally, from the salinity hazard potential analysis, most of the samples fell within C4 (based on the electrical conductivity), which is a "very high salinity" class, and based on the quality it means the water cannot be directly applied for irrigation purposes. From the 0.5 m column depth, most of the samples fell within C3 (the "high salinity" class), and from the 1 m column depth most of the samples fell within C1 ("low salinity" class). The findings of this study offer some valuable insight into the prospective use of natural zeolite for the filtration of saline groundwater before its application for irrigation.

Effect of calcium on enhanced carbon capture potential of coal fly ash zeolites. Part II: a study on the adsorption mechanisms.

Coal fly ash zeolites (CFAZs) of type X with low (Na-X) and medium (Na-Ca-X) content of calcium were synthesized by alkaline conversion of lignite coal fly ash generated by combustion of lignite with lower and higher limestone amounts, extracted from different coal deposits and burned in separate thermal power plants. The concentration and state of Ca in the zeolites were investigated by energy dispersive X-ray (EDX) analysis and X-ray photoelectron spectroscopy (XPS). CFAZs Na-Ca-X with a medium Ca-content were found to outperform their lower calcium counterparts Na-X in terms of carbon capture capacity. This provoked our research interest in elucidating the role of Ca in the CO2 retaining mechanism. CFAZs Na-X and Na-Ca-X were studied in consecutive dynamic adsorption cycles, after thermal regeneration at a temperature of 80 °C, at which only the physically adsorbed CO2 molecules can be released. Desorption was investigated by thermogravimetric TG-DTG analyses over a wide temperature range. In situ Fourier-transform infrared (FTIR) spectroscopy was performed to elucidate the structural features of Na-X and Na-Ca-X CFAZs and the types of their accessible adsorption sites. It was found that the role of Ca is to increase the number of accessible Na+ cations in SII and SIII positions in the zeolites where they can simultaneously adsorb two CO or CO2 molecules, which benefits their adsorption capacity. This study raises an issue on coal ash classification for the synthesis of zeolites with carbon capture applications.

Mercury Determination in Natural Zeolites by Thermal Decomposition Atomic Absorption Spectrometry: Method Validation in Compliance with Requirements for Use as Dietary Supplements.

Natural zeolites are hydrated aluminosilicate minerals that, due to their remarkable physical-chemical properties of being molecular sieves and cation exchangers, have applications in different areas such as environmental protection, catalysis, animal feed, and dietary supplements. Since natural zeolites may contain traces of undesirable compounds such as toxic metals, the accurate quantification of these elements is necessary. In this study, a direct method for Hg determination in zeolite samples based on the thermal desorption atomic absorption spectrometry (TD-AAS) technique is fully validated, taking into account the legislative requirements in the field. The chosen quantification limit was 0.9 µg kg-1, which is satisfactory for intended use. Trueness was evaluated by recovery rate using certified reference materials containing mercury, with satisfactory results. Other figures of merit, such as repeatability and measurement uncertainty, also fulfill the legislative requirements related to the analysis of dietary supplements. This paper presents, for the first time, a fully validated method for mercury determination in zeolite samples, and the obtained results reveal that the method can be applied successfully for the intended purpose.

Disinfection and removal performance for Escherichia coli, toxic heavy metals and arsenic by wood vinegar-modified zeolite.

Zeolite has traditionally been used to remediate wastewater and soil. The present study shows a new method for natural zeolite (NZ) modification with wood vinegar (WV). The optimal conditions for NZ modification with WV were determined, and the adsorption capacities towards lead (Pb), cadmium (Cd) and arsenic (As), antimicrobial activities against Escherichia coli, heavy metal(loid) fraction and characterizations of selected modified zeolites (MZs) were also investigated. The results indicate that 50-fold dilution of WV, 5 g of NZ dosage, 105 °C of drying temperature, 4 h and 95 °C of water bath are preferred for NZ modification with WV. The WV+NaOH-MZ exhibited the best performance in heavy metal removal and the most powerful antimicrobial activity among all the zeolites. The sequence of WV+NaOH-MZ for the maximum single metal(loid) adsorption capacities was Pb (48.67 mg/g) >Cd (23.67 mg/g) > As (0.024 mg/g). The WV+NaOH and WV modifications also can increase the stabilities of heavy metals in the MZs. The residual fractions of single Pb and Cd in WV+NaOH-MZ and WV-MZ were 50%, 55%, 34% and 30%, respectively. The pore size of WV+NaOH-MZ (11.73 nm) was bigger than that of NZ or WV-MZ. Additionally, the proportion of clinoptilolite in WV+NaOH-MZ was also higher than other zeolites. The surfaces of WV+alkali-MZs were rougher than that of NZ. Considering the low cost and environmental risk of WV, this work provides some useful information for management of agricultural and industrial residues, environment and food safety.

A high sensitivity system for luminescence measurement of materials.

A unique combined and multi-disciplinary wavelength multiplexed spectrometer is described. It is furnished with high-sensitivity imaging plate detectors, the power to which can be gated to provide time-resolved data. The system is capable of collecting spectrally resolved luminescence data following X-ray excitation [radioluminescence (RL) or X-ray excited optical luminescence (XEOL)], electron irradiation [cathodoluminescence (CL)] and visible light from light emitting diodes (LEDs) [photoluminescence (PL)]. Time-resolved PL and CL data can be collected to provide lifetime estimates with half-lives from microsecond timeframes. There are temperature stages for the high and low temperature experiments providing temperature control from 20 to 673 K. Combining irradiation, time resolved (TR) and TR-PL allows spectrally-resolved thermoluminescence (TL) and optically stimulated luminescence (OSL). The design of two detectors with matched gratings gives optimum sensitivity for the system. Examples which show the advantages and multi-use of the spectrometer are listed. Potential future experiments involving lifetime analysis as a function of irradiation, dose and temperature plus pump-probe experiments are discussed.

Manganese soil and foliar fertilization of olive plantlets: the effect on leaf mineral and phenolic content and root mycorrhizal colonization.

BACKGROUND: The present study aimed to examine the effect of foliar (Mn_fol) and soil Zeolite-Mn (Mn_ZA) application on leaf mineral, total phenolic and oleuropein content, and mycorrhizae colonization of self-rooted cv. Leccino plantlets grown on calcareous soil. RESULTS: The dissolution of zeolite was 97% when citric acid was applied at 0.05 mM dm-3 , suggesting that organic acids excreted by roots can dissolve modified zeolite (Mn_ZA), making Mn available for plant uptake. The leaf Mn concentration was the highest for Mn_fol treatment at 90 days after transplanting (DAT) (172 mg kg-1 ) and 150 DAT (70 mg kg-1 ) compared to other treatments. Mn_ZA soil application increased leaf Mn concentration at 150 DAT compared to control and NPK treatments. The oleuropein leaf content was highest for Mn_fol compared to other treatments at 90 DAT and lowest at 150 DAT. Arbuscular mycorrhizal colonization was higher for Mn_fol treatment at 150 DAT compared to all other treatments. CONCLUSION: Changes in the arbuscular colonization percentage and oleuropein content may be connected to stress conditions provoked by a high leaf Mn concentration in the Mn_fol treatment at 90 DAT. Mn_ZA application increased leaf Mn concentration at 150 DAT compared to control and NPK treatments. It can be assumed that the dominant mechanism in Mn uptake from modified zeolite is Mn_ZA dissolution through root exudates. © 2018 Society of Chemical Industry.

Nanocompósitos magnéticos para concentração/remoção de contaminantes de águas / Magnetic adsorbent nanocomposites for water treatment

Zeólitas e carvão ativado são materiais eficazes para o tratamento de efluentes devido a sua grande área superficial e possibilidades de funcionalização, que permitem o desenvolvimento de novos materiais derivados visando a processos de concentração/remoção de contaminantes, por exemplo, em águas. A preparação de nanocompósitos magnéticos e sua aplicação na remoção seletiva de poluentes em meio aquoso tornou-se viável devido as interações distintas que ocorrem entre zeólita e carvão ativado com compostos orgânicos, íons metálicos e compostos nitrogenados. Assim, novos materiais voltados para sistemas de tratamento de águas residuais e monitoramento ambiental foram desenvolvidos com base em materiais bem estabelecidos. Os nanocompósitos foram caracterizados estrutural e morfologicamente por técnicas de microscopia eletrônica de varredura, termogravimetria, espectroscopia no infravermelho, espalhamento de luz, difração de raios x, bem como suas capacidades de adsorção. Foi avaliado também a viabilidade de aplicações em métodos analíticos, como pré-concentração por extração em fase sólida magnética (M-SPE), e, para tratamento de efluentes em amostras reais. Contaminação por cromo (VI), outras espécies potencialmente tóxicas e amônio foram removidos de águas residuais, gerando produtos tratados com níveis de contaminantes suficientemente baixos para atenderem as recomendações da EPA (Environmental Protection Agency) e CONAMA (Conselho Nacional do Meio Ambiente), permitindo seu descarte na natureza. Os materiais demonstraram ser adequados para pré-concentração rápida, eficiente, economicamente competitiva e ambientalmente amigável de amostras por M-SPE para quantificação analítica de espécies orgânicas ou inorgânicas, por técnicas analíticas convencionais. Assim, foi demonstrado a possibilidade de determinação simultânea de elementos potencialmente tóxicos e de outros cátions metálicos em concentrações traço (ppb), diretamente no material compósito magnético, por espectroscopia de fluorescência de raios X de energia dispersiva (EDX), além da quantificação de traços de compostos orgânicos semi-voláteis por cromatografia emfase gasosa com detector por espectrometria de massas, aumentando a sensibilidade para além do limite nominal de detecção por essas técnicas

Zeolites and activated carbon are effective materials for the treatment of effluents due to their large surface area and functionalisation possibilities, which allow the development of new derived materials aiming at the concentration/removal of contaminants from water, for example. The preparation of magnetic nanocomposites and their application in the selective removal of pollutants in aqueous media has become feasible due to the distinct interactions that occur between zeolite and activated carbon with organic compounds, metal ions and nitrogen compounds. Thus, new materials for wastewater treatment and environmental monitoring systems were developed based on well-established materials. The nanocomposites were structural and morphologically characterized by scanning electron microscopy, thermogravimetry, infrared spectroscopy, light scattering, x-ray diffraction, as well as their adsorption capacities, viability of applications in analytical methods such as preconcentration by extraction in magnetic solid phase, M-SPE, were evaluated, and the composite materials Cmag and Zmag applied for treatment of real samples. Chromium (VI) contamination, heavy metal cations and ammonium were removed from wastewater, generating treated products with levels of contaminants low enough to meet the EPA and CONAMA recommendations, allowing their disposal in the wild. The materials have been shown to be suitable for rapid, efficient, economically competitive and environmentally friendly preconcentration of samples per M-SPE for analytical quantification of organic or inorganic species by conventional analytical techniques. Thus, it was demonstrated the possibility of simultaneous analysis of heavy metals and other metal cations in trace concentrations (ppb), directly in the magnetic composite material, by dispersive energy X-ray fluorescence spectroscopy (EDX), in addition to the quantification of traces of volatile organic compounds (VOC) by gas chromatography with mass spectrometry detector, increasing the sensitivity beyond the nominal limit of detection by these techniques

Using natural clinoptilolite zeolite as an amendment in vermicomposting of food waste.

The effect of adding different proportions of natural clinoptilolite zeolite (5 and 10%) to food waste vermicomposting was investigated by assessing the physicochemical characteristics, worms' growth, and maturation time of finished vermicompost in comparison with the vermicompost prepared with no amendment (control). Vermicomposting was performed in 18 plastic containers for 70 days. The experimental results showed that the carbon-to-nitrogen (C/N) ratios were 15.85, 10.75, and 8.94 for 5 and 10% zeolite concentration and control after 70 days, respectively. The addition of zeolite could facilitate organic matter degradation and increase the total nitrogen content by adsorption of ammonium ions. Increasing the proportion of zeolite from 0% (control) to 10% decreased the ammonia escape by 25% in the final vermicompost. The natural zeolite significantly reduced the electrical conductivity (EC). At the end of the process, salinity uptake efficiency was 39.23% for 5% zeolite treatment and 45.23% for 10% zeolite treatment. The pH values at 5 and 10% zeolite-amended treatments were 7.31 and 7.57, respectively, in comparison to 7.10 in the control. The maturation time at the end of vermicomposting decreased with increasing zeolite concentration. The vermicompost containing 5 and 10% zeolite matured in 49 and 42 days, respectively, in comparison to 56 days for the control. With the use of an initial ten immature Eisenia fetida worms, the number of mature worms in the 10% zeolite treatment was 26 more than that in the 5% zeolite treatment (21 worms) and 9 more than that in the control treatment (17 worms). Significantly, natural zeolite showed a beneficial effect on the characteristics of the end-product when used in the vermicomposting of food waste.

Assessing occupational erionite and respirable crystalline silica exposure among outdoor workers in Wyoming, South Dakota, and Montana.

Erionite is a naturally occurring fibrous mineral found in many parts of the world, including the western United States. Inhalational exposure to erionite fibers in some localities is associated with health effects similar to those caused by asbestos exposure, including malignant mesothelioma. Therefore, there is concern regarding occupational exposures in the western United States. Currently, there are no standard sampling and analytical methods for airborne erionite fibers, as well as no established occupational exposure limits. Due to the potential adverse health effects, characterizing and minimizing exposures is prudent. Crystalline silica also occurs naturally in areas where erionite is found, principally as the mineral quartz. Work activities involving rocks containing quartz and soils derived from those rocks can lead to exposure to respirable crystalline silica (RCS). The typically dry and dusty environment of the western United States can increase the likelihood of exposures to aerosolized rocks and soils, but inhalation exposure is also possible in more humid conditions. In this case study, we describe several outdoor occupational environments with potential exposures to erionite and RCS. We describe our method for evaluating those exposures and demonstrate: (1) the occurrence of occupational exposures to airborne erionite and RCS, (2) that the chemical make-up of the erionite mineral can be determined, and (3) that effective dust control practices are needed to reduce employee exposures to these minerals.

Iron-impregnated zeolite catalyst for efficient removal of micropollutants at very low concentration from Meurthe river.

In this paper, for the first time, faujasite Y zeolite impregnated with iron (III) was employed as a catalyst to remove a real cocktail of micropollutants inside real water samples from the Meurthe river by the means of the heterogeneous photo-Fenton process. The catalyst was prepared by the wet impregnation method using iron (III) nitrate nonahydrate as iron precursor. First, an optimization of the process parameters was conducted using phenol as model macro-pollutant. The hydrogen peroxide concentration, the light wavelength (UV and visible) and intensity, the iron loading immobilized, as well as the pH of the solution were investigated. Complete photo-Fenton degradation of the contaminant was achieved using faujasite containing 20 wt.% of iron, under UV light, and in the presence of 0.007 mol/L of H2O2 at pH 5.5. In a second step, the optimized process was used with real water samples from the Meurthe river. Twenty-one micropollutants (endocrine disruptors, pharmaceuticals, personal care products, and perfluorinated compounds) including 17 pharmaceutical compounds were specifically targeted, detected, and quantified. All the initial concentrations remained in the range of nanogram per liter (0.8-88 ng/L). The majority of the micropollutants had a large affinity for the surface of the iron-impregnated faujasite. Our results emphasized the very good efficiency of the photo-Fenton process with a cocktail of a minimum of 21 micropollutants. Except for sulfamethoxazole and PFOA, the concentrations of all the other microcontaminants (bisphenol A, carbamazepine, carbamazepine-10,11-epoxide, clarithromycin, diclofenac, estrone, ibuprofen, ketoprofen, lidocaine, naproxen, PFOS, triclosan, etc.) became lower than the limit of quantification of the LC-MS/MS after 30 min or 6 h of photo-Fenton treatment depending on their initial concentrations. The photo-Fenton degradation of PFOA can be neglected. The photo-Fenton degradation of sulfamethoxazole obeys first-order kinetics in the presence of the cocktail of the other micropollutants.

Avaliação da forma de inclusão de zeólita e do nível de consumo sobre a digestibilidade da dieta e as características fecais de cães / Evaluation of zeolite inclusion and level of food intake on diet digestibility and faecal characteristics of dogs

Objetivou-se avaliar a forma de inclusão da zeólita e de níveis de consumo sobre a digestibilidade da dieta e as características fecais de cães. O experimento 1 avaliou o efeito do nível de consumo (normal e 50% a mais do que as necessidades) e da inclusão de zeólita (0 e 15g/kg) sobre a digestibilidade e as características fecais de 12 cães. No experimento 2, foi avaliada a inclusão de 5, 15 e 25g/kg de zeólita adicionada na massa ou por cobertura, em seis cães, sobre a digestibilidade da dieta e as características fecais. O experimento 3 avaliou o odor fecal de nove cães consumindo dietas contendo 0 e 15g/kg de zeólita incluída na massa ou por cobertura. A quantidade consumida e a inclusão de zeólita não afetaram a digestibilidade das dietas. O escore e a matéria seca fecal aumentaram com a inclusão de zeólita. A inclusão de zeólita na massa propiciou aumento na digestibilidade das dietas, independentemente do nível de inclusão. A inclusão de 15g/kg de zeólita, adicionada na massa e por cobertura reduziu o odor fecal dos cães. A inclusão de zeólita na massa aumenta a digestibilidade da dieta, a consistência fecal e reduz o odor fecal de cães.(AU)

This study aimed to evaluate the form of inclusion of zeolite and consumption levels on diet digestibility and fecal characteristics of dogs. The first experiment examined the effect of consumption level (normal and 50% higher than the requirements) and zeolite level (0 and 15g/kg) on diet digestibility and fecal characteristics of 12 dogs. In experiment 2 the inclusion of 5, 15 and 25g/kg of added zeolite in dough or coating in six dogs on diet digestibility and fecal characteristics was evaluated. The third experiment assessed the fecal odor of nine dogs fed diets containing 0 and 15g/kg of zeolite included in the dough or coating. The amount consumed, as well as the inclusion of zeolite, did not affect diet digestibility. Fecal score and dry matter increased with the inclusion of zeolite. The inclusion of zeolite in the dough provided an increase in diet digestibility, regardless of the level of inclusion. The inclusion of 15g/kg zeolite added to the dough and by coating reduced fecal odor of dogs. The inclusion of zeolite in dough increases diet digestibility, fecal consistency, and reduces the fecal odor of dogs.(AU)

Geological occurrence, mineralogical characterization, and risk assessment of potentially carcinogenic erionite in Italy.

Erionite is a zeolite representing a well-known health hazard. In fact, exposure of humans to its fibers has been unequivocally associated with occurrence of malignant mesothelioma. For this reason, a multi-methodological approach, based upon field investigation, morphological characterization, scanning electron microscopy (SEM)/energy-dispersive spectroscopy (EDS) chemical analysis, and structure refinement through X-ray powder diffraction (XRPD), was applied to different samples of potentially carcinogenic erionite from Northern Italy. The studied crystals have a chemical composition ranging from erionite-Ca to erionite-Na and display variable morphologies, varying from prismatic, through acicular and fibrous, to extremely fibrous asbestiform habits. The fibrous samples were characterized by an unusual preferred partition of aluminum (Al) at tetrahedral site T1 instead of tetrahedral site T2. Further, a mismatch between the a-parameter of erionite-Ca and levyne-Ca that are intergrown in the asbestiform sample was detected. This misfit was coupled to a relevant micro-strain to maintain structure coherency at the boundary. Erionite occurs in 65% of the investigated sites, with an estimated quantity of 10 to 40 vol% of the associated minerals. The presence of this mineral is of concern for risk to human health, especially if one considers the vast number of quarries and mining-related activities that are operating in the zeolite host rocks. The discovery of fibrous and asbestiform erionite in Northern Italy suggests the need for a detailed risk assessment in all Italian areas showing the same potential hazard, with specific studies such as a quantification of the potentially respirable airborne fibers and targeted epidemiological surveillance.

Zeólitas naturais na dieta de frangos de corte / Natural zeolites in broiler diet

O objetivo deste trabalho foi avaliar o efeito da inclusão de 0,5% da zeólita natural clinoptilolita na dieta de frangos de corte sobre o consumo de água, ração e características das excretas. Foi conduzido um ensaio em gaiolas metabólicas, com frangos de corte de linhagem comercial, no período de 14 a 23 dias de idade. O experimento foi constituído de dois grupos de aves, sendo que um recebeu dieta sem inclusão de zeólitas (controle) e outro dieta com inclusão de 0,5% de zeólita (clinoptilolita) em rações isonutritivas, em um delineamento inteiramente ao acaso, com 10 repetições de 10 aves. Avaliou-se o consumo de água e de ração, nas excretas, pH, teor de nitrogênio total e umidade. A inclusão de 0,5% de zeólitas naturais na dieta não alterou (P>0,05) o consumo de água e de ração e o teor de nitrogênio das excretas, entretanto, reduziu (P<0,05) o pH e a umidade das excretas. Conclui-se que a inclusão de 0,5% de zeólitas naturais na dieta de frangos de corte reduz o pH e a umidade das excretas e pode ser utilizada como aditivo alimentar sem prejudicar o consumo de água e de ração.(AU)

The aim of this study was to evaluate the addition of 0.5% natural zeolites (clinoptilolite) to the diet of broilers and their effect on water and feed intake and excreta characteristics. The test was carried out in metabolic cages, with commercial line broilers, in the period from 14 to 23 days old. The experiment was conducted with two groups of broilers: one group received diet without zeolite inclusion (control) and the other received a diet with 0.5% inclusion of zeolite (clinoptilolite) in balanced diets, in a completely randomized design, with 10 replicates of 10 broilers. Water and feed intake, pH, total nitrogen, and moisture of excreta were evaluated. The inclusion of 0.5% of natural zeolites in the diet did not change (P>0.05) the water and feed intake and total nitrogen of excreta, nevertheless, it decreased (P<0.05) the pH and moisture of excreta. We conclude that the addition of 0.5% natural zeolites to the diet of broilers decreases pH and moisture of excreta and can be used as feed additive without compromising water and feed intake.(AU)

Influence of sodalite zeolite infiltration on the coefficient of thermal expansion and bond strength of all-ceramic dental prostheses.

In all-ceramic systems, a high incidence of veneer chip-off has been reported in clinical studies. Coefficient of thermal expansion (CTE) behaviour is one of the factors that may increase residual stress in the interface and influence the veneer/core bond strength. Therefore, this study aimed to evaluate the effect of sodalite zeolite-infiltration on the CTE behaviour and bond strength of different all-ceramic prostheses. The case-study groups were synthesized sodalite zeolite-infiltrated alumina (IA-SOD) and synthesized sodalite zeolite-infiltrated zirconia-toughened alumina (ZTA) (IZ-SOD), while the control groups were glass-infiltrated alumina (IA-glass) and glass-infiltrated ZTA (IZ-glass). Forty cylindrical-shaped samples measuring 5 mm in diameter and 10 mm in height were tested for CTE using a thermo-mechanical analyser machine, and forty disc-shaped ceramic samples measuring 12 mm in diameter and 1.2 ± 0.2 mm in thickness were prepared using specially designed stainless steel split mould and veneered by cylinder-shaped (2 mm high × 2 mm diameter) low-fusing porcelain (Vita VM7). The veneer/core samples were sintered and tested for shear bond strength using a high precision universal testing machine. Scanning electron microscope, stereo microscope, atomic force microscope, and energy-dispersive X-ray spectroscopy were used to investigate the structural characteristics of samples at the fracture surface. The collected data were analyzed with a one-way ANOVA and Tukey HSD test (α=.05). IZ-SOD revealed highest CTE and shear bond strength values, while the IA-glass revealed the lowest values than the other groups. There was no significant difference in CTE and bond strength among IZ-SOD, IA-SOD and IZ-glass samples (p>0.05). The experimental SOD zeolite-infiltrated samples revealed higher CTE mismatch and bond strength along with a more favourable mode of failure than did the commercial glass-infiltrated samples. Sandblast technique is considered as effective conditioning procedure for enhancing the surface roughness of SOD zeolite-infiltrated frameworks which subsequently improving the bond strength.

Potential carcinogenic erionite from Lessini Mounts, NE Italy: Morphological, mineralogical and chemical characterization.

Exposure of humans to erionite fibers of suitable morphology and dimension has been unambiguously linked to the occurrence of malignant mesothelioma. For this reason, a morphological, morphometrical, mineralogical, and chemical investigation was performed on two representative samples of potential carcinogenic, fibrous erionite from Lessini Mounts, northeastern (NE) Italy, which has not apparently been examined previously. The first sample is erionite-Ca with an extremely fibrous, hair-like and flexible appearance, and growth in intimate association with levyne. The second sample is erionite-Ca with prismatic to acicular crystals and rigid behavior, enriched in K(+) and Ca(2+) extra-framework cations. Although erionite is a nominally Fe-free phase, iron (Fe) was detected in low amounts in all the analyzed crystals. In both the investigated samples, erionite is present as individual fibers of respirable size. Considering that the toxicity and carcinogenic potential of erionite is associated with its size parameters, together with its in vivo durability and high surface area, most of the investigated fibers may also be potentially carcinogenic. The presence of erionite in extensively quarried and largely employed volcanic rocks, suggesting the need for detailed health-based studies in the region.

Optimizing the crystallinity and acidity of H-SAPO-34 by fluoride for synthesizing Cu/SAPO-34 NH3-SCR catalyst.

A series of H-SAPO-34 zeolites were synthesized by a hydrothermal method in fluoride media. The as-synthesized H-SAPO-34 zeolites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), N2 physisorption, temperature-programmed desorption of NH3 (NH3-TPD) and nuclear magnetic resonance (NMR) measurements. The results showed that a certain concentration of F(-) anions promoted the nucleation and crystallization of H-SAPO-34. The H-SAPO-34 synthesized in the fluoride media showed high crystallinity, uniform particle size distribution, large specific surface area and pore volume, and enhanced acidity. Therefore, Cu/SAPO-34 based on the fluoride-assisted zeolite showed a broadened temperature window for the selective catalytic reduction of NO by NH3 (NH3-SCR) reaction due to the enhanced acidity of the zeolite and the improved dispersion of copper species.

A Fungal-Prokaryotic Consortium at the Basalt-Zeolite Interface in Subseafloor Igneous Crust.

We have after half a century of coordinated scientific drilling gained insight into Earth´s largest microbial habitat, the subseafloor igneous crust, but still lack substantial understanding regarding its abundance, diversity and ecology. Here we describe a fossilized microbial consortium of prokaryotes and fungi at the basalt-zeolite interface of fractured subseafloor basalts from a depth of 240 m below seafloor (mbsf). The microbial consortium and its relationship with the surrounding physical environment are revealed by synchrotron-based X-ray tomographic microscopy (SRXTM), environmental scanning electron microscopy (ESEM), and Raman spectroscopy. The base of the consortium is represented by microstromatolites-remains of bacterial communities that oxidized reduced iron directly from the basalt. The microstromatolites and the surrounding basalt were overlaid by fungal cells and hyphae. The consortium was overgrown by hydrothermally formed zeolites but remained alive and active during this event. After its formation, fungal hyphae bored in the zeolite, producing millimetre-long tunnels through the mineral substrate. The dissolution could either serve to extract metals like Ca, Na and K essential for fungal growth and metabolism, or be a response to environmental stress owing to the mineral overgrowth. Our results show how microbial life may be maintained in a nutrient-poor and extreme environment by close ecological interplay and reveal an effective strategy for nutrient extraction from minerals. The prokaryotic portion of the consortium served as a carbon source for the eukaryotic portion. Such an approach may be a prerequisite for prokaryotic-eukaryotic colonisation of, and persistence in, subseafloor igneous crust.

High incidence of lung cancer and malignant mesothelioma linked to erionite fibre exposure in a rural community in Central Mexico.

OBJECTIVE: To report the high incidence of lung cancer (LC) and malignant mesothelioma (MM) linked to environmental exposure to erionite fibres in a rural village of central Mexico. METHODS: This is a retrospective survey of clinical and mortality records from the years 2000-2012, accompanied by an environmental survey for nine Group-1 lung and pleura carcinogenic agents listed by the International Agency for Research on Cancer (IARC). RESULTS: Out of a total of 45 deaths between 2000 and 2012, 14 deaths correspond to different neoplasms of the lung, and at least four deaths to MM. The ages at diagnosis of MM were between 30 and 54 years. Annual age-standardised mortality rates per thousand due to LC and MM in the village (age >20 years) are 7.09 and 2.48 for males, and 4.75 and 1.05 for females, respectively. Erionite fibres were found in exposed rocks and soils, which can easily become airborne and be carried into streets and recreational areas near schools and homes. Other carcinogenic elements and minerals are found only in trace amounts, except for quartz dust and asbestos (chrysotile) cement sheeting, which are also present in the neighbouring villages. CONCLUSIONS: These results indicate that environmental exposure to erionite is the main cause of the high rates of MM mortality in the Village of Tierra Blanca, supporting previous similar reports for people exposed to erionite fibres in villages in Turkey.