Some observations of the effects of pore fluids on the triaxial behaviour of a sand

This paper describes unusual stress–strain behaviour, involving deviatoric stress, axial strain and pore pressure jumps, observed during undrained triaxial compression testing of Leighton Buzzard sand when using syrup and silicon oil pore fluids. The materials, pore fluids, specimen preparation and test methods are described, as are the results of a suite of triaxial tests in a temperature controlled cell in which deviatoric stress, pore pressure and local strain were measured. The results are compared with the some existing data showing similar effects, and possible causes of the strain jumps are postulated. The results suggest that specimen formation in the way used here, in a viscous fluid, could suppress dilatancy.     

Enhanced dyeability of poly(ethylene terephthalate)/organoclay nanocomposite filaments

This study deals with the generation of poly(ethylene terephthalate)/organoclay nanocomposite filaments by the melt‐spinning method and with the investigation of their morphological and dyeing properties. Different montmorillonite types of clay (Resadiye and Rockwood) were modified using different intercalating agents, and poly(ethylene terephthalate) nanocomposite filaments containing 0.5 and 1 wt% organoclays were prepared. Afterwards, the filaments were dyed with two disperse dyes (Setapers Red P2G and Setapers Blue TFBL‐NEW) at different temperatures (100, 110, and 120 °C) in the absence/presence of a carrier. Organoclays and poly(ethylene terephthalate)/organoclay nanocomposites showed an increased d‐spacing between clay layers. Irrespective of clay and surfactant type, poly(ethylene terephthalate)/organoclay nanocomposite filaments dyed at 120 °C in the presence of only a very small amount of carrier showed appreciable dyeability in comparison with neat poly(ethylene terephthalate). The dyeability of the organoclay‐containing poly(ethylene terephthalate) samples was found to be better in spite of having increased degrees of crystallinity. Moreover, the colour fastness properties of the clay‐containing samples were not affected adversely.     

The investigation of coal-pyrite/lignite concentration and their separation in the artificial mixture by oil agglomeration

In this study, the concentration of coal-pyrite and lignite taken from Yozgat-Ayridam (Turkey) Coal Management was investigated by oil agglomeration.In the previous studies, the agglomeration of coal-pyrite was investigated using different bridging liquids (fuel oil, diesel oil and kerosene) and the combination of reagent (KEX, Acorga M5397)+kerosene. When using only bridging liquids, the agglomeration recovery of pyrite was very low. To increase the hydrophobicity of pyrite, KEX was used. However, the pyrite was not agglomerated with an acceptable recovery. But when using Acorga M5397, which is a chelating reagent, the agglomeration recovery of pyrite was increased. The pyrite was agglomerated with a recovery of 76.70 wt% by single-stage agglomeration.In the optimum conditions which were determined for coal-pyrite, the agglomeration recovery of lignite was investigated. It was found that the lignite could not be agglomerated with an acceptable recovery.To investigate the separation of coal-pyrite and lignite, the artificial mixture of coal-pyrite and lignite was prepared with the weight ratio of 1/4 of coal-pyrite and lignite. It was found that the pyrite could be agglomerated at a recovery of 96.54% with three-stage agglomeration process. The lignite concentrate was produced with a recovery of 73.96 wt% and the pyrite content of 0.86 wt%.These findings showed that the coal-pyrite and lignite could be separated by oil agglomeration using appropriate reagent and bridging liquid.     

Production of 2-hydroxyethyl methacrylate-g-poly(ethylene terephthalate) nanofibers by electrospinning and evaluation of the properties of the obtained nanofibers

Nanofiber production was investigated from poly(ethylene terephthalate) (PET) polymers functionalized with hydroxyethyl methacrylate (HEMA) by grafting of HEMA monomers onto the PET fibers. HEMA grafted PET (PET-g-HEMA) copolymers were analyzed by scanning electron microscopy, Fourier transform infrared spectroscopy, nuclear magnetic resonance spectroscopy. PET and PET-g-HEMA were dissolved in trifluoroacetic acid and nanofibers were obtained by electrospinning. It was found that the PET and PET-g-HEMA polymers having grafting yield 20 and 55% could be converted to continuous, smooth, and beadles nanofibers. For characterization of the nanofiber membranes, thermogravimetric analysis, differential scanning calorimeter analysis, surface contact angle measurement, porosity analysis, and mechanical tests were applied. When compared with the original PET nanofibers, the thermal properties and degradation process of PET-g-HEMA nanofibers changed according to the amount of HEMA present in the structure of nanofibers. The contact angles of the nanofibers obtained from PET-g-HEMA polymers decreased whereas the water retention ability of the nanofibers increased compared to original PET nanofibers. The porosity of PET-g-HEMA nanofibers was found be high compared to PET nanofibers and whereas the mechanical properties of PET was higher than PET-g-HEMA nanofibers. The obtained nanofibers can be used in many fields such as biomaterial applications.     

Poly(vinylidene fluoride) nanofiber-based piezoelectric nanogenerators using reduced graphene oxide/polyaniline

Recently, piezoelectric nanogenerators have received great interest as they can convert waste mechanical and radiative energy to electricity and can be used in self-energy generating systems and sensor technologies. In this study, electrospun poly(vinylidene fluoride) (PVDF) nanofiber-based piezoelectric nanogenerators with reduced graphene oxide (rGO), polyaniline (PANI), and PANI-functionalized rGO (rGOPANI) have been developed. Two different types of nanofiber mats were produced: First, rGO- and rGOPANI-doped PVDF nanofiber mats and second, rGO, PANI and rGOPANI-spray-coated PVDF nanofiber mats that have worked as nanogenerators' electrodes. Then, characterizations of samples were performed in terms of piezoelectricity, Fourier transform infrared (FTIR) spectrophotometric, X-ray diffractions (XRD), and scanning electron microscopy analyses. FTIR and XRD results confirmed that piezoelectric β-crystalline phase of PVDF occurred after the electrospinning process. Besides, maximum output voltages were obtained as 7.84 and 10.60 V for rGO-doped PVDF and rGOPANI-coated PVDF nanofiber mats, respectively. As a result, the doped nanofibers were found to be more successful due to the higher device accuracy in sensor technologies compared with spray-coated samples. However, spray-coating method proved to be more suitable technique for the production of nanogenerators on an industrial scale in terms of fast and large-scale applicability. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48517.     

Incorporating sepiolite and kaolinite to improve the performance of SPEEK composite membranes for proton exchange membrane fuel cells

SPEEK polymer based thermally crosslinked polymer membranes are prepared by sol-gel synthesis using kaolinite and sepiolite clays as additives. Characterization tests, ie, mechanical stability, thermal gravimetric analysis, ion exchange capability, swelling properties, water uptake capacities, electrochemical impedance spectroscopy analysis, and Fourier transform infrared spectroscopy (FTIR) analysis of the membranes were conducted. The sepiolite and kaolinite addition enhanced the thermal stability and the thermal crosslinking reduced the swelling capacity of the synthesized membranes. Proton conductivity results were increased from 0.172 to 0.268 S cm⁻¹ by adding 9% of kaolinite, and to 0.329 S cm⁻¹ at 80°C by adding 9% of sepiolite to the SPEEK membrane's polymer structure. The fuel cell current density and potential measurements of 141 mA cm⁻² and 84.6 mW cm⁻² were found respectively at 0.6 V for the SPEEK/S9 membrane, whereas values of 600 mA cm⁻² and 348 mW cm⁻² were found for the Nafion commercial membrane.     

Evaluation of synthesized new chitin derivatives in Schottky diode constructions

ABSTRACT

Chitin was reacted with coumarin-3-carboxylic acid (C3CA) and benzophenone-3,3?,4,4?-tetracarboxylic dianhydride (B33?44?TD), and the synthesized chitin derivatives (CC3CA and CB33?44?TD) were characterized by spectroscopic methods and other techniques (FTIR, ¹³C CP/MAS solid-state NMR, XRPD, SEM, and TGA). Also, the charge carrier density, hole mobility, and electrical conductivity of CB33?44?TD were determined. Lastly, Schottky diodes were constructed using these derivatives, and some electrical properties (barrier height, ideality factor, and series resistance) and photoelectrical properties (light sensitivity, short circuit current, and open circuit voltage) of the diodes were determined. It was seen that the diodes have very good ideality factor and light sensitivity.     

The illumination intensity and applied bias voltage on dielectric properties of au/polyvinyl alcohol (Co,Zn‐doped)/n‐Si Schottky barrier diodes

The Au/polyvinyl alcohol (PVA) (Co, Zn‐doped)/n‐Si Schottky barrier diodes (SBDs) were exposed to various illumination intensities. Illumination effect on the dielectric properties has been investigated by using capacitance–voltage (C–V) and conductance–voltage (G/ω–V) characteristics at 1 MHz and room temperature. The values of dielectric constant (ε′), dielectric loss (ε″), loss tangent (tanδ), electric modulus (M′ and M″), and AC electrical conductivity (σ_AC) were found strongly intensity dependent on both the illumination levels and applied bias voltage especially in depletion and accumulation regions. Such bias and illumination dependency of these parameters can be explained on the basis of Maxwell–Wagner interfacial polarization and restructuring and reordering of charges at interface states. In addition, the ε′–V plots also show an intersection feature at ～ 2.8 V and such behavior of the ε′–V plots appears as an abnormality compared with the conventional behavior of an ideal SBD. The obtained results revealed that illumination intensity enhances the conductivity of Au/PVA(Co, Zn‐doped)/n‐Si SBD. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

A polymeric nanocomposite system for potential adhesive applications in restorative dentistry

This article presents and discusses the preliminary results obtained as a continuation of a work aiming to contribute to the effort of exploring the potential of certain types of polymer nanocomposites to be successful candidates in new fields such as dental restoration. An epoxy-functional silicate-/Zr-based polymeric nanocomposite material system containing phosphorus was obtained via a sol–gel method, and applied to bring about a bonding between bovine teeth and feldspathic ceramic discs with or without the use of visible light (VL)-curing process. Infrared spectroscopy was employed to show the presence of phosphorus within the structure. Mechanical tests were performed to determine the shear-bond strength of the nanocomposite adhesive system developed. An approximate shear-bond strength value of 0.4 MPa was obtained for both VL-cured and uncured systems. Though this value was lower than that of commercially available material systems, it was promisingly comparable to them. Another significant finding was that the material system developed within the study might potentially eliminate the use of curing process. Also, it was demonstrated that the general problem of ‘shrinkage-upon-polymerization’ could be overcome by use of a polymeric nanocomposite adhesive material system of this type. Overall results indicated that this polymeric nanocomposite system could indeed be potentially considered as an adhesive alternative in prospective dental restoration applications.