Geopolymers: A new and smart way for a sustainable development

“Geopolymers” is a general term that describes a wide variety of inorganic and composite materials with limited restrictions on alumina and silica content. In the last decades, they have been also defined as “low-temperature aluminosilicate glasses”, “hydroceramics”, “inorganic polymer concrete” or “alkali bonded ceramics”. Recently, an updated definition has been proposed by the RILEM Technical Committee 224-AAM: “geopolymer materials are essential aluminosilicates activated with alkaline solution, excluding any other alkali-activated materials that should be classified apart” [1]

Carrier thermal escape in families of InAs/InP self-assembled quantum dots

We investigate the thermal quenching of the multimodal photoluminescence from InAs/InP (001) self-assembled quantum dots. The temperature evolution of the photoluminescence spectra of two samples is followed from 10 K to 300 K. We develop a coupled rate-equation model that includes the effect of carrier thermal escape from a quantum dot to the wetting layer and to the InP matrix, followed by transport, recapture or non-radiative recombination. Our model reproduces the temperature dependence of the emission of each family of quantum dots with a single set of parameters. We find that the main escape mechanism of the carriers confined in the quantum dots is through thermal emission to the wetting layer. The activation energy for this process is found to be close to one-half the energy difference between that of a given family of quantum dots and that of the wetting layer as measured by photoluminescence excitation experiments. This indicates that electron and holes exit the InAs quantum dots as correlated pairs

The origin of the E+ transition in GaAsN alloys

Optical properties of GaAsN system with nitrogen concentrations in the range of 0.9-3.7% are studied by full-potential LAPW method in a supercell approach. The E+ transition is identified by calculating the imaginary part of the dielectric function. The evolution of the energy of this transition with nitrogen concentration is studied and the origin of this transition is identified by analyzing the contributions to the dielectric function from different band combinations. The L_1c-derived states are shown to play an important role in the formation of the E+ transition, which was also suggested by recent experiments. At the same time the nitrogen-induced modification of the first conduction band of the host compound are also found to contribute significantly to the E+ transition. Further, the study of several model supercells demonstrated the significant influence of the nitrogen potential on the optical properties of the GaAsN system.Comment: 5 pages, 3 figure

Partial Hydrogenation of Soybean and Waste Cooking Oil Biodiesel over Recyclable-Polymer-Supported Pd and Ni Nanoparticles

Biodiesel obtained through the transesterification in methanol of vegetable oils, such as soybean oil (SO) and waste cooking oil (WCO), cannot be used as a biofuel for automotive applications due to the presence of polyunsaturated fatty esters, which have a detrimental effect on oxidation stability (OS). A method of upgrading this material is the catalytic partial hydrogenation of the fatty acid methyl ester (FAME) mixture. The target molecule of the partial hydrogenation reaction is monounsaturated methyl oleate (C18:1), which represents a good compromise between OS and the cold filter plugging point (CFPP) value, which becomes too high if the biodiesel consists of unsaturated fatty esters only. In the present work, polymer-supported palladium (Pd-pol) and nickel (Ni-pol) nanoparticles were separately tested as catalysts for upgrading SO and WCO biodiesels under mild conditions (room temperature for Pd-pol and T = 100◦ C for Ni-pol) using dihydrogen (p = 10 bar) as the reductant. Both catalysts were obtained through co-polymerization of the metal containing monomer M(AAEMA)2 (M = Pd, Ni; AEEMA− = deprotonated form of 2-(acetoacetoxy)ethyl methacrylate)) with co-monomers (ethyl methacrylate for Pd and N,N-dimethylacrilamide for Ni) and cross-linkers (ethylene glycol dimethacrylate for Pd and N,N’-methylene bis-acrylamide for Ni), followed by reduction. The Pd-pol system became very active in the hydrogenation of C=C double bonds, but poorly selective towards the desirable C18:1 product. The Ni-pol catalyst was less active than Pd-pol, but very selective towards the mono-unsaturated product. Recyclability tests demonstrated that the Ni-based system retained its activity and selectivity with both the SO and WCO substrates for at least five subsequent runs, thus representing an opportunity for waste biomass valorization

A Multi-Physic Modelling Insight into the Differences between Microwave and Conventional Heating for the Synthesis of TiO2 Nanoparticles

Microwave-assisted synthesis of nanoparticles usually leads to a smaller and more uni-formly distributed particle size compared to conventional heating (e.g., oil bath). Numerical simulation can help to obtain a better insight into the process in terms of temperature distribution or to evidence existing different temperature profiles and heating rates between the two techniques. In this paper multi-physics numerical simulation is used to investigate the continuous flow synthesis of titanium oxide nanoparticles starting from alkoxide precursors. Temperature-dependent permit-tivity of reactants has been measured, including the effects of permanence at the maximum synthesis temperature. A temperature homogeneity index has been defined to compare microwave and conventional heating. Results show that when using microwave heating at 2450 MHz, in the inves-tigated conditions, a much higher temperature homogeneity of the reactants is reached. Moreover, reactants experience different heating rates, depending on their position inside the microwave ap-plicator, while this is almost negligible in the case of conventional heating

. Microwave-assisted solvothermal controlled synthesis of Fe-Co

Syntheses of bimetallic cobalt-iron-based nanoparticles starting from Co(acac)2 and Fe(acac)3 (acac = acetylacetonate) were carried out by microwave-assisted solvothermal process, using ethylene glycol as the solvent and (polyvinylpyrrolidone) PVP, as the stabilizer. Indeed, the reaction mechanism in the presence of ethylene glycol is well understood [1] with the role of PVP being the inhibition of nanoparticles growth [2]. However, the control of the morphology of the synthetized nanoparticles is still a great challenge. Herein, we demonstrated that by adding amines to the reaction mixture, it is possible to control the morphology of the prepared bimetallic cobalt-iron materials. Thus, different Co-Fe micro-composites were synthetized by an innovative microwave assisted solvothermal synthesis, which allows to considerably reduce reaction time from 12 h to 15 min, with respect to classical thermal methods. The procedure was optimized by varying several parameters, such as: amount of PVP, in the presence or in the absence of amines, reaction temperature. The dark brown obtained powders were characterized by scanning electron microscopy, infrared spectroscopy and thermogravimetric analysis, confirming the beneficial effect of the presence of the amine in the morphology of the obtained composites. The obtained results open a new scenario for further studies on the possibility to control the morphology of bimetallic composite materials. [1] Fievet F, Lagier J P and Figlarz M Mater. Res. Soc. Bull. 24 (1989) 29–34 [2] Teranishi T, Kurita R and Miyake M J. Inorg. Organometall. Polym. 10 (2000) 145–5

Photovoltaic Pumps: Technical and Practical Aspects for Applications in Agriculture

The paper deals with a series of tests conducted on a PV-DC pump in Viterbo (42°24′ North, 12°06′ East). The tests lasted from January 2003 up to November 2004 and involved measurements of solar radiation, on both a horizontal surface and the tilted module surface, flow rates, volumes, and total dynamic heads. In total, up to 3000 data were collected every day whose analysis allowed us to find empirical relationships among system efficiencies, solar radiations, and total dynamic heads. In the second part of the paper we develop a simple method that allows both the assessment of performances of the whole system when installed in a different site from that in which the tests were performed and the optimal inclination angle of the panel to be determined in relation to annual or seasonal use (see irrigation)