Dielectric and mechanical optimization properties of porous poly(ethylene‐co‐vinyl acetate) copolymer films for pseudo‐piezoelectric effect

In this article, the authors present a porous copolymer film with pseudo‐piezoelectric effects as a new candidate material for sensing applications. Porous films of poly(ethylene‐co‐vinyl acetate) (EVA) with a thicknesses ranging from 160 to 310 μm are fabricated by a coextrusion chemical foaming process and charged using a high‐voltage contact charging process. Output performances (piezoelectric constant and relative permittivity) with related thermal/mechanical stability are specifically studied as a function of the film porosity and of the electrical charging process. The piezoelectric constant d₃₃ increases with the cell porosity and an interesting piezoelectric constant close to 5.1 pC/N is achieved with a porous EVA film containing 65% of porosity. Actual results are then discussed using a theoretical solid–gas multilayer model to describe and predict the pseudo‐piezoelectric effect of porous polymer materials. The originality of this work lies in the fact that all the steps leading to optimize pseudo piezoelectric films are included, and also in the use of EVA which is not a standard piezoelectric material. Therefore, this work is a contribution in the development of low‐cost piezoelectric materials with potential applications as sensor in different fields such as medical, security, environment, sport, and transport. POLYM. ENG. SCI., 59:1455–1461 2019. © 2019 Society of Plastics Engineers     

Protein Denaturation in Pork Longissimus Muscle of Different Quality Groups

Differential scanning calorimetry (DSC) was used to investigate the protein denaturation characteristics of pork muscles from four quality groups namely RFN (red, firm, and non-exudative), RSE (red, soft, and exudative), PFN (pale, firm, and non-exudative), and PSE (pale, soft, and exudative). The thermograms indicated three endothermic peaks between 45°C to 90°C, corresponding to denaturation of myosin (peak I), sarcoplasmic proteins (peak II), and actin (peak III). The myosin peak was much reduced in PSE samples, while the actin peak remained almost identical in all groups. RFN and RSE samples were found to have very similar protein denaturation characteristics and were not significantly different in their thermodynamic protein denaturation parameters. PFN samples showed similar myofibrilar protein denaturation but significantly different sarcoplasmic protein denaturation characteristics compared to normal (RFN) samples according to their DSC thermograms. Based on these findings, it was suggested that the pale color in PFN pork is linked to sarcoplasmic protein denaturation.     

Biomimetic Zirconia with Cactus-Inspired Meso-Scale Spikes and Nano-Trabeculae for Enhanced Bone Integration

Biomimetic design provides novel opportunities for enhancing and functionalizing biomaterials. Here we created a zirconia surface with cactus-inspired meso-scale spikes and bone-inspired nano-scale trabecular architecture and examined its biological activity in bone generation and integration. Crisscrossing laser etching successfully engraved 60 μm wide, cactus-inspired spikes on yttria-stabilized tetragonal zirconia polycrystal (Y-TZP) with 200–300 nm trabecular bone-inspired interwoven structures on the entire surface. The height of the spikes was varied from 20 to 80 μm for optimization. Average roughness (Sa) increased from 0.10 μm (polished smooth surface) to 18.14 μm (80 μm-high spikes), while the surface area increased by up to 4.43 times. The measured dimensions of the spikes almost perfectly correlated with their estimated dimensions (R² = 0.998). The dimensional error of forming the architecture was 1% as a coefficient of variation. Bone marrow-derived osteoblasts were cultured on a polished surface and on meso- and nano-scale hybrid textured surfaces with different spike heights. The osteoblastic differentiation was significantly promoted on the hybrid-textured surfaces compared with the polished surface, and among them the hybrid-textured surface with 40 μm-high spikes showed unparalleled performance. In vivo bone-implant integration also peaked when the hybrid-textured surface had 40 μm-high spikes. The relationships between the spike height and measures of osteoblast differentiation and the strength of bone and implant integration were non-linear. The controllable creation of meso- and nano-scale hybrid biomimetic surfaces established in this study may provide a novel technological platform and design strategy for future development of biomaterial surfaces to improve bone integration and regeneration.     

Pure and complex nanostructures using poly[bis(triiso‐propylsilylethynyl) benzodithiophene‐bis(decyltetradecyl‐thien) naphthobisthiadiazole], carbon nanotubes and reduced graphene oxide for high‐performance polymer solar cells

Crystallization of poly[bis(triiso‐propylsilylethynyl) benzodithiophene‐bis(decyltetradecyl‐thien) naphthobisthiadiazole] (PBDT‐TIPS‐DTNT‐DT) was investigated in supramolecules based on carbon nanotubes (CNTs) and reduced graphene oxide (rGO) and their grafted derivatives. The principal peaks of PBDT‐TIPS‐DTNT‐DT crystals were in the range 3.50°–3.75°. By grafting the surface of the carbonic materials, the assembling of polymer chains decreased because of hindrance of poly(3‐dodecylthiophene) (PDDT) grafts against π‐stacking. The diameters of CNT/polymer and CNT‐g‐PDDT/polymer supramolecules were 160 and 100 nm. The rGO/polymer supramolecules had the highest melting point (T_m = 282 °C) and fusion enthalpy (ΔH_m = 25.98 J g^?1), reflecting the largest crystallites and the most ordered constituents. Nano‐hybrids based on grafted rGO (276 °C and 28.26 J g^?1), CNT (275 °C and 27.32 J g^?1) and grafted CNT (268 °C and 22.17 J g^?1) were also analyzed. T_m and ΔH_m values were significantly less in corresponding melt‐grown systems. The nanostructures were incorporated in active layers of PBDT‐TIPS‐DTNT‐DT:phenyl‐C₇₁‐butyric acid methyl ester (PC₇₁BM) solar cells to improve the photovoltaic features. The best results were detected for PBDT‐TIPS‐DTNT‐DT:PC₇₁BM:rGO/polymer systems having J_sc = 13.11 mA cm^?2, fill factor 60% and V_oc = 0.71 V with an efficacy of 5.58%. On grafting the rGO and CNT, efficiency reductions were 12.01% (5.58%–4.91%) and 9.34% (4.07%–3.69%), respectively. © 2019 Society of Chemical Industry     

TAMER: an adaptive task allocation method for aging reduction in multi-core embedded real-time systems

The Journal of Supercomputing - Technology scaling has exacerbated the aging impact on the performance and reliability of integrated circuits. By entering into nanotechnology era in recent years,...     

Hydrolytic degradation of poly(l‐lactic acid)/poly(methyl methacrylate) blends

The hydrolytic degradation of poly(l ‐lactic acid)/poly(methyl methacrylate) (PLLA/PMMA) blends was carried out by the immersion of thin films in buffer solutions (pH = 7.24) in a shaking water bath at 60 °C for 38 days. The PLA/PMMA blends (0/100; 30/70; 50/50; 70/30; 100/0) were obtained by melt blending using a Brabender internal mixer and shaped into thin films of about 150 µm in thickness. Considering that PMMA does not undergo hydrolytic degradation, that of PLLA was followed via evolution of PLA molecular weight (recorded by size exclusion chromatography), thermal parameters (differential scanning calorimetry (DSC)) and morphology of the films (scanning transmission electron microscopy). The results reveal a completely different degradation pathway of the blends depending on the polymethacrylate/polyester weight ratio. DSC data suggest that, during hydrolysis at higher PMMA content, the polyester amorphous chains, more sensitive to water, are degraded before being able to crystallize, while at higher PLLA content, the crystallization is favoured leading to a sample more resistant to hydrolysis. In other words, and quite unexpectedly, increasing the content of water‐sensitive PLLA in the PLLA/PMMA blends does not mean de facto faster hydrolytic degradation of the resulting materials. © 2018 Society of Chemical Industry     

Spurenstoffabtrennung mit keramischen Nanofiltrationsmembranen als Rotationsscheibenfilter

Reducing micropollutant pollution of water bodies is an important objective of water management and an integral part of environmental policy. Ceramic nanofiltration membranes were developed as multichannel membranes of increased membrane area and rotating disk filters. The membranes developed show retention of over 80 % for PEG 400. The membranes are currently being tested for the separation of micropollutants from wastewater contaminated with pharmaceuticals. With the help of a downstream oxidative process, the trace substances remaining in the permeate are degraded.     

Experimental investigation of far-field human cough airflows from healthy and influenza-infected subjects

Seasonal influenza epidemics have been responsible for causing increased economic expenditures and many deaths worldwide. Evidence exists to support the claim that the virus can be spread through the air, but the relative significance of airborne transmission has not been well defined. Particle image velocimetry (PIV) and hot-wire anemometry (HWA) measurements were conducted at 1 m away from the mouth of human subjects to develop a model for cough flow behavior at greater distances from the mouth than were studied previously. Biological aerosol sampling was conducted to assess the risk of exposure to airborne viruses. Throughout the investigation, 77 experiments were conducted from 58 different subjects. From these subjects, 21 presented with influenza-like illness. Of these, 12 subjects had laboratory-confirmed respiratory infections. A model was developed for the cough centerline velocity magnitude time history. The experimental results were also used to validate computational fluid dynamics (CFD) models. The peak velocity observed at the cough jet center, averaged across all trials, was 1.2 m/s, and an average jet spread angle of θ = 24° was measured, similar to that of a steady free jet. No differences were observed in the velocity or turbulence characteristics between coughs from sick, convalescent, or healthy participants.     

Electroactive polythiophene/polystyrene bottlebrushes as morphology compatibilizers in photovoltaic systems

Poly(3‐thiophene ethanol) (P3ThEt)‐graft‐polystyrene (PSt) bottlebrushes were synthesized and applied in active layers of poly(3‐hexylthiophene) (P3HT):phenyl‐C71‐butyric acid methyl ester (PC71BM) solar cells as morphology compatibilizers. In the presence of 15 wt% of P3ThEt‐graft‐PSt bottlebrush compatibilizers, the P3HT crystallite dimensions (D₍₁₀₀₎ = 45.67 nm and D₍₀₂₀₎ = 30.12 nm) and R_mean (38.96 nm) of PCBM clusters were the largest and the layer spacings were all the smallest (d₍₁₀₀₎ = 1.054 nm, d₍₀₂₀₎ = 0.301 nm and d_(PCBM) = 0.406 nm). These dimensional properties led to better hole (1.9 × 10^?3 cm² V^?1 s^?1) and electron (1.2 × 10^?2 cm² V^?1 s^?1) mobilities. The content of bottlebrushes was optimized at 15 wt%, and thereby the best photovoltaic results including the maximum cell efficiency of 5.37% were obtained for this turning point (12.75 mA cm^?2, 61%, 0.69 V). On exceeding the optimum weight percentage, all photovoltaic parameters decreased markedly and reached even less than that of pristine devices (1.92% versus 2.24%). After an optimum weight percentage of compatibilizers, further enhancement in bottlebrush content in active layers saturated and finally oversaturated the system and, consequently, the cell parameters significantly decreased. Accumulation of bottlebrushes in interfaces and donor/acceptor phases ruined the system function even with large and packed P3HT crystallites and PC71BM clusters. © 2019 Society of Chemical Industry     

Improved stability in P3HT:PCBM photovoltaics by incorporation of well‐designed polythiophene/graphene compositions

Morphological and photovoltaic stabilities of poly(3‐hexylthiophene) (P3HT):phenyl‐C₆₁‐butyric acid methyl ester (PC₇₁BM) solar cells were investigated in pristine and modified states. To this end, four types of patterned/assembled nanostructures, namely reduced graphene oxide (rGO)‐g‐poly(3‐dodecylthiophene)/P3HT patched‐like pattern, rGO–polythiophene/P3HT/PC₇₁BM nanofiber, rGO‐g‐P3HT/P3HT cake‐like pattern and supra(polyaniline (PANI)‐g‐rGO/P3HT), were designed on the basis of rGO and various conjugated polymers. Intermediately covered rGO nanosheets by P3HT crystals (supra(PANI‐g‐rGO/P3HT)) performed better than sparsely (patched‐like pattern) and fully (cake‐like pattern) covered ones in P3HT:PC₇₁BM solar cell systems. Supra(PANI‐g‐rGO/P3HT) nanohybrids largely phase‐separated in active layers (root mean square = 0.88 nm) and also led to the highest performance (power conversion efficiency of 5.74%). The photovoltaic characteristics demonstrated decreasing trends during air aging for all devices, but with distinct slopes. The steepest decreasing plots were obtained for the unmodified P3HT:PC₇₁BM devices (from 1.77% to 0.28%). The two supramolecules with the most ordered structures, that is, cake‐like pattern (10.12 mA cm^?2, 51%, 0.58 V, 2.2 × 10^?6 cm² V^?1 s^?1, 4.3 × 10^?5 cm² V^?1 s^?1, 0.69 nm and 2.99%) and supra(PANI‐g‐rGO/P3HT) (12.51 mA cm^?2, 57%, 0.63 V, 1.2 × 10^?5 cm² V^?1 s^?1, 3.4 × 10^?4 cm² V^?1 s^?1, 0.82 nm and 4.49%), strongly retained morphological and photovoltaic stabilities in P3HT:PC₇₁BM devices after 1 month of air aging. According to the morphological, optical, photovoltaic and electrochemical results, the supra(PANI‐g‐rGO/P3HT) nanohybrid was the best candidate for stabilizing P3HT:PC₇₁BM solar cells. © 2020 Society of Chemical Industry