Kaolinite bioformation at surface conditions: The role of fungi and bacteria.

Experiments aimed at studying the role of microorganisms in the formation of kaolinite from aluminosilicate solutions (Si:Al = 1:1) are reported. The experiments were carried out at room temperature in presence of living microorganisms, Leonardite humic acid, bacterial debris, bacterial exopolysaccharides (EPS), and some organic ligands. The bacterial debris, EPS, Leonardite and organic ligands were chosen to stabilize Al in octahedral coordination for allowing the crystallization of kaolinite.

Direct Observations of Ordered Nanoporosity in Deprotonated 2-(Acetoacetoxy)ethyl Methacrylate (AAEMA) Polymer: Preliminary Results.

Polymers based on 2-(acetoacetoxy)ethyl methacrylate, charged with iron or sodium, were thermally heated at 150 °C. Both polymers were studied and characterized by SEM, TEM, STEM microscopy and SAEDF techniques. The morphological investigation revealed that, upon heating, both polymers were endowed with microholes, sometimes perfectly ordered, whose dimensions varied from 4-5 nm to approximately 500 nm.

In vivo functionalization of diatom biosilica with sodium alendronate as osteoactive material.

Bisphosphonates are a class of drugs widely used in the clinical treatment of disorders of bone metabolism, such as osteoporosis, fibrous dysplasia, myeloma and bone metastases. Because of the negative side effects caused by oral administration of bisphosphonates, various silica mesoporous materials have been investigated for a confined and controlled release of these drugs. Here, we propose biosilica from diatoms as suitable substrate for alendronate local activation of bone cells.

Data from functionalization of diatom mesoporous biosilica with bisphosphonates.

Diatoms are unicellular photosynthetic microalgae that produce a sophisticated mesoporous biosilica shell called . Easy to achieve and extract, diatom frustules represent a low-cost source of mesoporous biocompatible biosilica. In this paper, the possibility to functionalize the diatom biosilica with bisphosphonates (BPs) was investigated.

Sustainable bio-hydrothermal sequencing treatment for asbestos-cement wastes.

In this paper, the treatment of asbestos-cement waste (ACW) has been attempted by a dark fermentation (DF) pre-treatment followed by hydrothermal and anaerobic digestion (AD) treatments. During DF, glucose, employed as a biodegradable substrate, was mainly converted to H-rich biogas and organic acids (OAs). The latter caused the dissolution of the cement matrix and the partial structural collapse of chrysotile (white asbestos).

Are conventional statistical techniques exhaustive for defining metal background concentrations in harbour sediments? A case study: The Coastal Area of Bari (Southeast Italy).

Sediment contamination by metals poses significant risks to coastal ecosystems and is considered to be problematic for dredging operations. The determination of the background values of metal and metalloid distribution based on site-specific variability is fundamental in assessing pollution levels in harbour sediments. The novelty of the present work consists of addressing the scope and limitation of analysing port sediments through the use of conventional statistical techniques (such as: linear regression analysis, construction of cumulative frequency curves and the iterative 2σ technique), that are commonly employed for assessing Regional Geochemical Background (RGB) values in coastal sediments.

Environmental risk induced by TiO2 dispersions in waters and sediments: a case study.

A southern Italian area that is characterized by large outcrops of rocks that are rich in titanium oxide (TiO2) phases were investigated to determine the mineralogical risk induced by the natural dispersion of TiO2 minerals. Rock, sediment and surface water samples were collected to determine the physicochemical and mineralogical factors (i.e.

Removal of Mn from aqueous solution using fly ash and its hydrothermal synthetic zeolite.

A number of water purification processes have been developed in recent years based on the utilisation of low-cost materials with high pollutant removal efficiency. Among these materials, fly ash and zeolite synthesised from fly ash are two examples of high-efficiency adsorbents. Column absorption tests were performed in order to compare the manganese sorption behaviour of an Italian coal fly ash and zeolite synthesised from it.

Provenance of inorganic aerosol using single-particle analysis: a case study.

A total of 137 samples of airborne particulates with an aerodynamic equivalent diameter of 10 μm or less (PM10) were collected from April 2007 to July 2008 in four different areas (Potenza, Lavello, Viggiano, Matera) of the Basilicata region in southern Italy. A total of approximately 140,000 particles were analysed using a Field Emission Scanning Electron Microscope (FESEM) equipped with an Energy-Dispersive X-ray Spectrometer (EDS). To formulate a hypothesis on the origin of particles, the dataset was numerically reduced using mineralogical criteria.

Ultrasonic waves induce rapid zeolite synthesis in a seawater solution.

The synthesis of zeolites from fly ash was performed through a low-temperature hydrothermal process with seawater. Compared with the results obtained using the same hydrothermal method but in the absence of sonication, the application of an ultrasonic pre-treatment to the conventional hydrothermal process with seawater reduces the crystallization temperature below that observed when hydrothermal synthesis is performed using distilled water.

Effects of ultrasonic treatment on zeolite synthesized from coal fly ash.

The synthesis of zeolites from three samples of fly ash was carried out through a low-temperature (25-60°C) hydrothermal process with a NaOH pre-fusion treatment preceded by sonication. The results were compared with those of conventional hydrothermal syntheses. XRD and SEM investigations demonstrate that the application of ultrasonic treatment facilitates the formation of zeolites at a lower-temperature (25°C) than syntheses not preceded by sonication.

Immobilization of Ni by synthesising zeolite at low temperatures in a polluted soil.

Over the last few years a great deal of research has been carried out in order to develop remediation methods for reducing environmental risks due to polluting metals. Zeolite formation in contaminated soils mixed with coal fly ash could be a useful method to reduce both the availability and the mobility of metals in contaminated areas. In this study a soil sample--treated with coal fly ash and artificially contaminated with a high concentration of Ni--was used for synthesizing zeolite at low temperatures.

Synthesis of zeolite from Italian coal fly ash: differences in crystallization temperature using seawater instead of distilled water.

In this study Italian coal fly ash was converted into several types of zeolite in laboratory experiments with temperatures of crystallization ranging from 35 up to 90 degrees C. Distilled and seawater were used during the hydrothermal synthesis process in separate experiments, after a pre-treatment fusion with NaOH. The results indicate that zeolites could be formed from different kind of Italian coal fly ash at low temperature of crystallization using both distilled and seawater.

Assessing the origin and fate of Cr, Ni, Cu, Zn, Pb, and V in industrial polluted soil by combined microspectroscopic techniques and bulk extraction methods.

The major geochemical forms of Cr, Ni, Cu, Zn, Pb, and V in a soil from an industrial polluted site in the south of Italy were determined by means of synchrotron X-ray microanalytical techniques such as coupled micro-X-ray fluorescence/micro-X-ray diffraction and micro-X-ray absorption near edge structure spectroscopy in combination with bulk extraction methods (sequential extraction procedures, EDTA extractions, and toxicity leaching characteristic procedure tests). Cr, Ni, Zn, and Cu were found in spinel-type geochemical forms (chromite, trevorite, franklinite, zincochromite, and cuprospinel) and often in association with magnetite and hematite. Vwas mainly present as V(V) associated with iron-oxides or in the form of volborthite [Cu3(OH)2V2O7.