Preparation of Electrospun Electroactive Nanofibers of Four Arm Star-Shaped Poly(ε-Caprolactone)-b-Poly(2-Hydroxyethyl Methacrylate) and Its Blends with Polyaniline

A combination of ring-opening polymerization and atom-transfer radical polymerization was used to synthesize a four-arm star-shaped poly(ε-caprolactone)-b-poly(2-hydroxyethyl methacrylate). The structure of obtained copolymer was determined by Fourier transform infrared, ¹H and ¹³C NMR spectroscopies. The uniform electroactive nanofibers consisting blend of four-arm star-shaped poly(ε-caprolactone)-b-poly(2-hydroxyethyl methacrylate) copolymer and polyaniline were produced using electrospinning technique. The electroactivity of prepared nanofibers was investigated using cyclic voltammetry measurement. The morphologies of electrospun nanofibers produced from four-arm star-shaped poly(ε-caprolactone)-b-poly(2-hydroxyethyl methacrylate) and their blends with polyaniline were investigated by the scanning electron microscopy. The presence of polyaniline resulted in significant decrease of sticking fibers.     

Effect of seed layers on low-temperature,chemical bath deposited ZnO nanorods-based near UV-OLED performance

Low-temperature wet chemical bath deposition (CBD) method is one of the most efficient and least hazardous solution-based techniques which is widely employed to grow ZnO NRs. In CBD method, a seed layer is usually deposited on the substrate. In this paper, high quality ZnO and aluminum doped ZnO (AZO) seed layers are sputtered on the indium tin oxide (ITO) coated glass. In continue, aligned ZnO NRs are grown on the AZO and ZnO seed layers via CBD technique. The effect of the growth time and seed layer on the physical properties of as-grown ZnO NRs are investigated. According to the results, the seed layer plays an essential role on the growth orientation and growth rate of the ZnO NRs. The ZnO NRs grown on AZO seed layer are more aligned rather than ZnO seed layer due to their higher texture coefficients. The relative photoluminescence (PL) intensity ratio of near band emission (NBE) to deep level emission (DLE) (I_NBE/I_DLE) for the ZnO NRs grown on AZO and ZnO seed layers are calculated as 7.45 and 2.62, respectively. To investigate the performance of the as-grown ZnO NRs, near ultraviolet organic light-emitting diodes (UV-OLEDs) using ZnO NRs array as n-type material and poly [2-methoxy-5-(2-ethyl-hexyloxy)-1,4-phenylene-vinylene] (MEH-PPV) conjugated polymer as p-type material have been fabricated. The total concentration of traps ($N_t$), the characteristic energies ($E_t$) and the turn-on voltages for the devices with the structures of ITO/AZO/ZnO NRs/MEH-PPV/Al (device A) and ITO/ZnO/ZnO NRs/MEH-PPV/Al (device B) are attained 7.65 × 10¹⁶ and 7.75 × 10¹⁶ cm^?3, 0.232 and 0.206 eV, 23 and 21 V, respectively. Moreover, based on the electroluminescence (EL) spectra, the NBE peaks for device A and B are obtained nearly in the wavelengths of 382 and 388 nm, respectively. Finally, various charge carrier transportation processes of prepared UV-OLEDs have been studied, systematically.     

Mechanical characterization and modeling stress relaxation behavior of acrylic–polyurethane-based graft-interpenetrating polymer networks

The stress relaxation behavior of acrylic–polyurethane (PU)-based graft-interpenetrating polymer networks (IPNs) was characterized via dynamic mechanical analysis (DMA) and modeled using finite element method (FEM) analysis. Stress relaxation of glassy IPN specimens was experimentally studied under flexural testing, while rubbery IPN specimens were tested in tension. The effects of varying the styrene content in the acrylic copolymer phase, compatibility of the two phases in IPNs, and changing the concentration of acrylic copolymer and PU were studied. A higher percentage of styrene content resulted in higher homogeneity of IPN specimens, and decrease in initial modulus for acrylic copolymer specimens. Additionally, glassy IPN specimens with 90% styrene shows resistance to relaxation as high as acrylic copolymer samples. Experimental results were used to develop a numerical model to study stress relaxation response of specimens. While polymer systems have been studied computationally, numerical modeling of IPN systems is still in its infancy. A three-dimensional FEM model was developed using the Generalized Maxwell model and four-term Prony series constants, which were extracted from the stress relaxation experiments. With four terms in the Prony series, a good match was observed between experimental observations and results from the FEM model.     

Preformed particle gels of sulfonated polyacrylamide: preparation,characterization, and application as permeability modifier

In this study, a preformed particle gel (PPG) was synthesized from sulfonated polyacrylamide and chromium metal cross-linker with specific concentration. The main characteristics of PPG, such as gelation time, gel fraction, swelling properties and salt sensitivity factor were investigated. The gel fraction of 94.1% practically indicated an appropriate conversion of gelant to the gel. The equilibrium swelling ratios of particle gels in distilled water and formation water at 80 °C were 470.49 and 12.61, respectively. Additionally, the rheological properties of gel were studied by a dynamic rheometer. The ultimate storage modulus of gel was measured 35.4 kPa. The linear viscoelastic behavior was observed at strain between 1 and 82.6% and gel structure was stable up to strain of 1120% with small reduction of storage modulus. The kinetics of gelation were also studied at different temperatures and tested against Avrami equation to determine the kinetic parameters. The Avrami exponents for two kinetic steps were about 2.29 and 0.80, respectively, indicating the rapid formation of the gel network at first step due to nucleation and two-dimensional growths of gel nuclei. Furthermore, a core flooding experiment was conducted to study PPG performance in porous media. The residual resistance factor of water and oil was 41.58 and 12.91, respectively. A value of 3.22 for the ratio of these two factors indicated the ability of the synthesized PPG to decrease water-effective permeability compared to oil-effective permeability in porous media.

     

Heterogeneous Catalytic Polymerization of Ethylene in Microtubular Reactor Systems

The feasibility of using a microtubular reactor for heterogeneous polymerization of ethylene was investigated experimentally. Chemically inert polymer tubing of 800–2300 μm in inner diameter was fabricated and used as a polymerization reactor. Nonporous silica nanoparticles with a diameter of 400 nm were synthesized and used as support for the high‐activity rac‐ethylene(indenyl)₂ZrCl₂ catalyst with methylaluminoxane as cocatalyst and toluene as diluent. Large‐diameter microtubular reactors were also successfully used to conduct heterogeneous polymerization of ethylene in continuous reaction operations. High initial catalyst activity was obtained and the overall polymerization activity per volume or reactor length was quite high. No particle fragmentation occurred and the polymer particles were covered with small subgrains or nanofibrils with a diameter of 30 nm.     

Polyaniline/akaganéite nanocomposite for detoxification of noxious Cr(VI) from aquatic environment

In this work, a removal of toxic hexavalent chromium Cr(VI) ion from aqueous solution was investigated and studied using nanocomposite of polyaniline (PANI) and akaganéite nanoparticles (NP). HCl doped PANI, and akaganéite NPs were prepared by chemical oxidative polymerization and co-precipitation techniques, respectively. The synthesized materials were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscope (SEM), and high-resolution transmission electron microscope (HRTEM). It was indicated that the formed oxide NPs were consisted of akaganéite as dominant phase plus minor phases of hematite, magnetite, and/or maghemite. HRTEM images of the prepared nanocomposite demonstrated that the phases of oxide NPs embedded in the nanocomposite had the same crystallinity and morphology of pristine oxide NPs. It was found that size of nanocomposite particles has diameter ranged from 8.95 to 16.21 nm. Cr(VI) removals in a wide pH range from 2 to 9 were appropriated for prepared nanocomposite. The nanocomposite has demonstrated high removal percentage of 99.2 % and removal capacity of 17.36 mg/g for 7.0 mg/L Cr(VI) polluted aqueous solution at pH 2.0 for 5-min contact time. The synthesized nanocomposite was applied to remove Cr(VI) from a leather tanning wastewater sample with efficiency of 93.4 %.     

The odontogenic differentiation of human dental pulp stem cells on hydroxyapatite-coated biodegradable nanofibrous scaffolds

The authors aimed to design nanofibrous (NF) scaffolds that facilitate odontogenic and osteogenic differentiation of human dental pulp-derived mesenchymal stem cells (DPSCs) in vitro. For this purpose, hydroxyapatite (HA)–loaded poly (L-lactic acid)/poly (?-caprolactone) (PLLA:PCL 2;1) blend NFs were prepared using the electrospinning method. Alizarin red activity and cell viability were evaluated by MTT assay, and SEM revealed the proliferation properties of NF scaffolds. QRT-PCR results demonstrated that HA-loaded PLLA/PCL can lead to osteoblast/odontoblast differentiation in DPSCs through the up-regulation of related genes, thus indicating that electrospun biodegradable PCL/PLA/HA has remarkable prospects as scaffolds for bone and tooth tissue engineering.     

Electrical and structural properties of polyaniline/cellulose triacetate blend films

Polyaniline (PANI) has been blended with cellulose triacetate (CTA) to obtain both good mechanical properties and good electrical properties. The effects of PANI weight percentage on the optical, structural, morphological and electrical properties in the blend films of polyaniline and cellulose triacetate (PANI/CTA) have been investigated. The phenomenon of percolation was observed in these blend films. It is found that the electrical conductivity of the blend films increases with the increase of polyaniline content up to a value of 10⁻⁴ S cm⁻¹ at 84 weight percentage of PANI. The experimental percolation threshold of the dried blend films is obtained at 9.5 wt% of polyaniline. The values of Mott’s temperature, density of states at the Fermi level [N (E _f)], hopping distance (R _hop), and barrier height (W _hop) for PANI/CTA blend films are calculated. By applying Mott’s theory, it is found that the PANI/CTA blend films obey the three dimensional variable range hopping mechanism.     

Model tree approach for predicting uniaxial compressive strength and Young’s modulus of carbonate rocks

Bulletin of Engineering Geology and the Environment - The uniaxial compressive strength (UCS) and Young’s modulus (E) of rock are important parameters for evaluating the strength,...