Microwaves in Soil Remediation from VOC’s. 1. Heat and Mass Transfer Aspects.

A novel technique presented performs in situ remediation of soils contaminated by volatile organic compounds (VOCs) based on the use of electromagnetic fields for heating operations. Attention is focused on heat and mass transfer occurring in porousmoisturized media like a soil matrix. The microwave induced steam distillation process is investigated. Measurements are reported of temperature, humidity, residual contaminant concentration, and permittivity during the process. The crucial role is elucidated that the changes of the dielectrical properties of the soil matrix play on the electromagnetic field propagation. A mathematical model of the remediation process relating all the parameters above is proposed and validated. doi: 10.1002/aic.69049072

adhesion of functional layer on polymeric substrates for optoelectronic applications

The use of plastic film substrates for organic electronic devices promises to enable new applications, such as flexible displays. Plastic substrates have several distinct advantages, such as ruggedness, robustness, ultra lightness, conformability and impact resistance over glass substrates, which are primarily used in flat panel displays (FPDs) today. However, high transparency, proper surface roughness, low gas permeability and high transparent electrode conductivity of the plastic substrate are required for commercial applications. Polyesters, both amorphous and semicrystalline, are a promising class of commercial polymer for optoelectronic applications. Surface modification of polyester films was performed via chemical solution determining hydrolysis or oxidation. Hydrolysis was carried out by means of sodium hydroxide solution and oxidation by using standard clean 1 (SC-1) of RCA procedure [1]. For this work we have used commercial polymer films of 100µm in thickness: AryLite™ [2], supplied by Ferrania Imaging Technologies S.p.A. and characterised by very high glass transition temperature, Mylar™ (Polyethylene Terephthalate PET) and Teonex™ (Polyethylene Naphthalate PEN) both supplied by Dupont. More over, a bioriented and semicrystalline PET have been used. The aim of this study is modifying the polymer surface to improve the adhesion between organic-inorganic layer. It was found that the NaOH and SC-1 treatment cause a decrease of contact angles. In the present study we have deposited a thin films of amorphous hydrogenated silicon (a-Si:H) and its oxide (SiO2) on a new high temperature polymer substrate, AryLite™, by plasma enhanced chemical vapour deposition (PECVD) [3], with a radio frequency plasma system

INNOVATIVE TOOLS FOR MANAGING HISTORICAL BUILDINGS: THE USE OF GEOGRAPHIC INFORMATION SYSTEM AND ONTOLOGIES FOR HISTORICAL CENTERS

A recent study and the digitalization of historical centres have developed a completely new strategy for the conservation management of urban buildings through the ‘Risk Map’ of MiBAC. Issues, aims and structure of the Territory Information System (TIS) have been wholly outlined in a dedicated book that describes the structure of the system, also following a historical framing of the debate and the previous experiences. The elaboration of a dedicated ontology adds the opportunity to make the same data available to other kind of software, beginning from HBIM Systems. This aim is pursued developing a special extension of CIDOC-CRM, an already consolidated ontology initially dedicated to the conservation issue of museums. The work has firstly considered the field of architectural conservation and recently further developed addressing historical centres. In this way, a synthetic description of the buildings, including the main features together with vulnerability and transformation index, will allow, through the 3D representation of the town, a stable monitoring of the urban tissue, constantly up to date with the new data deriving from the interventions gradually realized

Using organoclay to promote morphology refinement and co-continuity in high-density polyethylene/polyamide 6 blends - Effect of filler content and polymer matrix composition

We investigate the gradual changes of the microstructure of two blends of high-density polyethylene (HOPE) and polyamide 6 (PA6) at opposite composition filled with increasing amounts of an organo-modified clay. The filler locates preferentially inside the polyamide phase, bringing about radical alterations in the micron-scale arrangement of the polymer phases. When the host polyamide represents the major constituent, a sudden reduction of the average sizes of the polyethylene droplets was observed upon addition of even low amounts of organoclay. A morphology refinement was also noticed at low filler contents when the particles distributes inside the minor phase. In this case, however, keep increasing the organoclay content eventually results in a high degree of PA6 phase continuity. Rheological analyses reveal that the filler loading at which the polyamide assembles in a continuous network corresponds to the critical threshold for its rheological transition from a liquid- to a gel-like behaviour, which is indicative of the structuring of the filler inside the host PA6. On the basis of this finding, a schematic mechanism is proposed in which the role of the filler in driving the space arrangement of the polymer phases is discussed. Finally, we show that the synergism between the reinforcing action of the filler and its ability to affect the blend microstructure can be exploited in order to enhance relevant technological properties of the materials, such as their high temperature structural integrit

Importance of the morphology and structure of the primary aggregates for the dispersibility of carbon nanotubes in polymer melts

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Dispersing hydrophilic nanoparticles in hydrophobic polymers: HDPE/ZnO nanocomposites by a novel template-based approach

The efficiency of a novel template-based approach for the dispersion of hydrophilic nanoparticles within hydrophobic polymer matrices is investigated. The procedure envisages the permeation of a well dispersed nanoparticle suspension inside a micro-porous matrix, obtained through selective extraction of a sacrificial phase from a finely interpenetrated co-continuous polymer blend. Specifically, a blend of high density polyethylene (HDPE) and polyethylene oxide (PEO) at 50/50 wt% is prepared by melt mixing. The addition of small amounts of organo-clay promotes the necessary refinement of the blend morphology. Once removed the PEO, the micro-porous HDPE matrix is dipped in a colloidal suspension of zinc oxide nanoparticles which exhibits low interfacial tension with HDPE. A system prepared by traditional melt mixing is used as reference. Melt- and solid-state viscoelastic measurements reveal a good quality of the filler dispersion despite the uneven distribution on micro-scale. The latter can be capitalized to minimize the filler content to attain a certain improvement of the material properties or to design nano-structured polymer composites. © BME-PT

Polyacetylenes Bearing Chiral-Substituted Fluorene and Terfluorene Pendant Groups: Synthesis and Properties

The synthesis of the first polyacetylenes bearing chiral fluorene-based pendant groups is described. Poly{9,9-bis[(S)-3,7-dimethyloctyl]fluoren-2-ylacetylene} (PFA1), poly{9,9-bis[(S)-2-methylbutyl]- fluoren-2-ylacetylene} (PFA2), and poly{9,9,9′,9′,9′′,9′′-hexakis[(S)-2-methylbutyl]-7,2′;7′,2′′-terfluoren- 2-ylacetylene} (PFA3) have been obtained by Rh(I)-catalyzed polymerization of the corresponding terminal acetylene monomers 2-ethynyl-9,9-bis[(S)-3,7-dimethyloctyl]fluorene (2a), 2-ethynyl-9,9-bis[(S)-2-methylbutyl]fluorene (2b), and 2-ethynyl-9,9,9′,9′,9′′,9′′-hexakis[(S)-2-methylbutyl]-7,2′;7′,2′′-terfluorene (10). The effect of the alkyl chain length at the C-9 position of fluorene on the structural and conformational aspects of the polymers PFA1 and PFA2 as well as on their chiroptical properties was studied by XRD, DSC, TGA, GPC, UV-vis, and CD. A more planar conformation of the polyenic backbone of PFA1 with respect to PFA2 can be inferred by a red shift of the ð-ð* transition in the UV-vis spectra. Their photoluminescence properties are those typical of fluorene systems. CD measurements evidenced Cotton effects of opposite signs in correspondence of the backbone absorption region, ascribable to an excess of a screw sense of the helical conformations assumed by the two polymers. PFA3 revealed an amorphous structure and exhibited peculiar thermal stability features (as indicated by TGA and DSC). Its emission spectra interest the violet-blue region and do not show any substantial red shift passing from solution to solid state, thus pointing out an aggregation prevention of terfluorene groups by means of the polyacetylene backbone