Hot corrosion behaviour of 7YSZ + Gd2O3 nano-composites in molten salts prepared by spark plasma sintering

This study compares the hot corrosion performance of yttria-stabilised zirconia (7YSZ), and 7YSZ?+?Gd₂O₃ composite samples in the presence of molten mixture of Na₂SO₄?+?V₂O₅ at 1150°C. For 7YSZ, the reaction between NaVO₃ and Y₂O₃ produces YVO₄ and leads the transformation of tetragonal ZrO₂ to monoclinic ZrO₂. A high-density in sintered 7YSZ?+?Gd₂O₃ samples, led minor amounts of monoclinic ZrO₂ and tetragonal GdVO₄ as the hot corrosion products with only traceable amounts of YVO₄, and a stable corroded layer was formed. Due to the synergic effect of doping of zirconia with Gd₂O₃, the 7YSZ?+?Gd₂O₃ sample has a much better hot corrosion crack resistance than 7YSZ.     

Preparation and electrical characterization of poly(vinyl amine) hydrogels,crosslinked with Cu(II) ions,and evaluation of their potentiality as water sensor material

A method to prepare water sensitive composites employing crosslinked poly(vinyl amine) (PVAm) and Cu(II) ions as reticulation agent is disclosed in this work. This article presents in detail, the reticulation reaction and its pH dependence, as well as its electrical, rheological, and thermal properties of the PVAm‐Cu(II) composites obtained. The complex bonds formed between the Cu(II) ions and the amine groups of PVAm produce an interesting network of crosslinked structures that generate a microporous morphology when the material is extruded. This characteristic favors fast absorption of water when it is wetted, and a concomitant decrease in its apparent resistivity in a very short period of time. Furthermore, they present an excellent thermal stability and suitable processability. These characteristics make them interesting candidates to design ultra fast water sensors. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Finite size effects in multilayered polymer systems: Development of PET lamellae under physical confinement

The glass transition temperature and the crystallization behaviour of poly(ethylene terephthalate) PET ultra-thin layers (a few tens of nm) within multilayered PET/polycarbonate (PC) coextruded films are investigated as a function of layer thickness by means of calorimetric measurements. Results are discussed in terms of reduced thickness and interface effects. The appearance and evolution of lamellar orientation upon isothermal crystallization of ultra-thin PET layers from the glassy state are explored based on real time small-angle X-ray scattering (SAXS) studies. Analysis of the SAXS measurements reveals that finite size effects hamper the crystallization process. However, the final lamellar structure is similar in both, the nanolayered PET and the bulk material. Results suggest that not only lamellar insertion but also some lamellar thickening contribute to the development of the final lamellar structure. Room temperature SAXS and wide-angle X-ray diffraction (WAXS) measurements indicate that two lamellar populations develop: edge-on lamellae are proposed to appear close to the interphases while flat-on lamellae, arising as a consequence of confinement, should be preferentially located in the layers core.     

Chemical,thermal, and mechanical properties and ultraviolet transmittance of novel nano-hydroxyapatite/polyethylene terephthalate milk bottles

Polyethylene terephthalate (PET)/nano-hydroxyapatite (nHAp) composite granules were obtained using twin-screw extruder. Preforms were prepared by injection molding and then PET/nHAp bottles were produced by blow molding. For PET bottles with nHAp, the migration amounts of carboxylic acid (COOH), acetaldehyde (AA), diethylene glycol (DEG), and isophthalic acid (IPA); glass transition temperature (T_g); melting temperature (T_m); and the maximum crystallization temperature (T_cry) were measured. The load-carrying capacity, burst strength, stress cracking, and regional material distribution tests were carried out on the bottles. X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, differential scanning calorimetry, and ultraviolet transmittance analyses were conducted to explain the changes in mechanical, chemical, physical properties, and light transmission of bottles. It was found out that the COOH amount increased and the AA content decreased with increasing nHAp amount. On the other hand, no change was observed in the amounts of DEG and IPA. Although the mechanical properties such as load-carrying capacity and burst strength of the bottles have improved, it has been determined that the standard environmental stress crack resistance test procedure cannot be applied to such a composite. Experimental findings indicate that nHAp disrupts the chemical structure of PET and it isolates harmful chemicals such as AA by forming intermolecular bonds. Moreover, with the addition of up to 0.8% nHAp, PET bottles block the light transmission approximately 80% within 400–700 nm wave length zone. The study demonstrates that the PET/nHAp composite bottles can be used in the food industry, particularly in the packaging of milk and milk products which are vulnerable to light exposure.     

Combining Electricity and Fuel Supply: Operational Strategies for Biogas Plants

The operational consequences resulting from the combination of a flexibly operated combined heat and power unit (CHP) and an off‐grid biomethane filling station at one biogas plant were investigated. Four different operating scenarios were compared to evaluate the storage capacity needed to balance biogas demand fluctuations and biogas production. The scenario in which fuel production was given priority and electricity was produced within the remaining hours proved to cause the lowest additional costs since it does not require additional installation of biogas storage capacity and causes minor opportunity cost in electricity marketing. Giving fuel demand the priority reduces the necessary biogas storage capacity by 75 % compared to parallel optimization of the electricity and fuel demands.     

Correction to: Two New Co(II) Complexes of Picolinate: Synthesis,Crystal Structure,Spectral Characterization, α-Glucosidase İnhibition and TD/DFT Study

Journal of Inorganic and Organometallic Polymers and Materials -     

Acoustical absorptive properties of spunbonded nonwovens made from islands-in-the-sea bicomponent filaments

In this paper, we report on the acoustical absorptive behavior of spunbonded nonwovens that contain bicomponent islands-in-the-sea filaments. Nylon 6 (PA6) and polyethylene were used as the islands and the sea polymers, respectively. Spunbonded webs made with islands-in-the-sea bicomponent filaments with island counts of 1, 7, 19, 37, and 108 were produced at the Nonwovens Institute’s pilot facilities at NC State University. The filaments were fibrillated by hydroentangling, where high-speed water jets were used to fibrillate the fiber and ‘free’ the islands. The influence of the number of islands on acoustical absorptive behavior of the spunbonded nonwovens was investigated. A comparison of acoustical absorptive properties of multi-layer islands-in-the-sea nonwoven and high loft nonwoven was also performed to evaluate the potential use of spunbonded nonwovens made from islands-in-the-sea bicomponent filaments in place of bulky fibrous sound absorbers. Results have shown that multi-layer 108 nonwoven islands were better acoustic absorbers at nearly half of the frequency range. Spunbonded nonwovens made from islands-in-the-sea bicomponent filaments can be a good alternative in applications where there is desire to replace bulky fibrous sound absorbers.