Maria Cristina Mascolo

Room Temperature Co-Precipitation Synthesis of Magnetite Nanoparticles in a Large pH Window with Different Bases

Magnetite nanoparticles (Fe3O4) represent the most promising materials in medical applications. To favor high-drug or enzyme loading on the nanoparticles, they are incorporated into mesoporous materials to form a hybrid support with the consequent reduction of magnetization saturation. The direct synthesis of mesoporous structures appears to be of interest. To this end, magnetite nanoparticles have been synthesized using a one pot co-precipitation reaction at room temperature in the presence of different bases, such as NaOH, KOH or (C2H5)4NOH. Magnetite shows characteristics of superparamagnetism at room temperature and a saturation magnetization (Ms) value depending on both the crystal size and the degree of agglomeration of individual nanoparticles. Such agglomeration appears to be responsible for the formation of mesoporous structures, which are affected by the pH, the nature of alkali, the slow or fast addition of alkaline solution and the drying modality of synthesized powders.

Thermal transformation of Ba-exchanged A and X zeolites into monoclinic celsian

Abstract The thermal transformation of Ba- and (Ba+Li)-exchanged precursors of zeolites A and X into monoclinic celsian has been investigated by X-ray diffractometry, differential thermal analysis, and thermodilatometry. Upon the proper thermal treatment either Ba-exchanged zeolite A or X give rise to the following transformations: zeolite→amorphous phase→hexacelsian→monoclinic celsian. Zeolite A-based precursors are more reactive than zeolite X-based precursors allowing all the reported transformations to occur at far lower temperatures starting from Ba-exchanged zeolite A rather than from Ba-exchanged zeolite X. In particular, starting from zeolite X-based precursors, fully monoclinic celsian may be obtained after 24 h at 1550°C in the absence of Li and after 6 h at 1100°C in the presence of Li, whereas starting from zeolite A-based precursors it may be obtained after 6 h at 1100°C in the absence of Li and by slow heating (1°C/min) up to 900°C in the presence of Li.

Binders alternative to Portland cement and waste management for sustainable construction—part 1:

This review presents “a state of the art” report on sustainability in construction materials. The authors propose different solutions to make the concrete industry more environmentally friendly in order to reduce greenhouse gases emissions and consumption of non-renewable resources. Part 1—the present paper—focuses on the use of binders alternative to Portland cement, including sulfoaluminate cements, alkali-activated materials, and geopolymers. Part 2 will be dedicated to traditional Portland-free binders and waste management and recycling in mortar and concrete production.

Recyclable Aggregates of Mesoporous Titania Synthesized by Thermal Treatment of Amorphous or Peptized Precursors

Recyclable aggregates of mesoporous titania with different anatase–rutile ratios have been prepared by thermal treatments of either amorphous or peptized precursors. These last two have been obtained by hydrolysis of either Ti(OC2H5)4 or of Ti(OC2H5)4 in mixture with 5 mol % Zr(OC3H7)4 at room temperature in the presence of NH4OH as a catalyzing agent. The anatase–rutile ratio, the recyclable aggregates of the nano-sized particles, the mesoporosity, the surface area and the crystallinity of the resulting crystallized products of titania can be controlled by the synthesis parameters including: concentration of ammonia catalyst, stirring time and concentration of the peptizing HNO3, drying method of peptized precursors, calcination temperature, and finally the ramp rate up to the titania crystallization temperature. A broad range of synthesis parameters control the crystal sizes of titania particles produced. This allows catalyst preparation with very different crystal size, surface area, anatase to rutile crystal ratio and various mesoporous structures. Drying by lyophilization of precursors reduce the aggregation of the primary particles giving micro-/macroporous structures.

Proton Conductivity of Amorphous Hydrated Zirconia-Yttria Solid Solutions

Mechanical mixtures of zirconia xerogel with variable content of crystalline Y2O3 up to 25 mol%, were hydrothermally treated by microwave route at 110 °C for 2 hours in the presence of 0.2 M solution of (KOH+K2CO3) mineralizer. The resulting amorphous hydrated zirconia-yttria solid solutions with a maximum solubility of Y2O3 content between 20 ~ 25 mol%, showed a remarkable reduction of the surface area at the increasing Y2O3 content of the starting mixture. The as-synthesized products and the corresponding calcined powders at 400 °C were uniaxially pressed into pellets (10 x 7 x 2 ~ 4 mm, in width) at 150 MPa. Conductivities were measured at 25 °C by AC impedance method with a frequency range from 10 Hz to 1 MHz with the pellets equilibrated either under silica gel or under increasing relative humidity (RH) up to ~90 %. The effects of composition, surface area, calcination temperature and relative RH on the proton conductivity of the amorphous solid solutions are discussed.