Evaluation of rheological and image properties of styrene‐butadiene‐styrene and ethylene‐vinyl acetate polymer modified bitumens

This article presents a laboratory evaluation of conventional, fundamental, rheological, and morphological characteristics of styrene‐butadiene‐styrene (SBS) and ethylene vinyl acetate (EVA) polymer modified bitumens. Polymer modified bitumen (PMB) samples have been produced by mixing a 50/70 penetration grade unmodified (base) bitumen with SBS and EVA copolymer at different polymer contents. The fundamental viscoelastic properties of the PMBs were determined using dynamic (oscillatory) mechanical analysis and presented in the form of temperature and frequency‐dependent rheological parameters. The morphology of the samples as well as the percent area distribution of polymers throughout the base bitumen have been characterized and determined by means of fluorescent light optic microscopy and Qwin Plus image analysis software, respectively. The results indicated that polymer modification improved the conventional and rheological properties of the base bitumen. It was also concluded that the temperature and frequency had a significant effect on complex modulus of PMBs. The behavior of EVA and SBS PMBs had exhibited quite difference at 50°C. Moreover, it was found out that at low polymer contents, the samples revealed the existence of dispersed polymer particles in a continuous bitumen phase, whereas at high polymer contents a continuous polymer phase has been observed. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Entrapment of urease in poly(1‐vinyl imidazole)/poly(2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid) network

In this article, urease was immobilized in a conducting network via complexation of poly(1‐vinyl imidazole) (PVI) with poly(2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid) (PAMPS). The preparation method for the polymer network was adjusted by using Fourier transform infrared (FTIR) spectroscopy. A scanning electron microscope (SEM) study revealed that enzyme immobilization had a strong effect on film morphology. The proton conductivity of the PVI/PAMPS network was measured via impedance spectroscopy, under humidified conditions. The basic characteristics (Michealis‐Menten constants, pH_opt, pH_stability, T_opt, T_stability, reusability, and storage stability) of the immobilized urease were determined. The obtained results showed that the PAA/PVI polymer network was suitable for enzyme immobilization. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Surface modification of polyester and polyamide fabrics by low frequency plasma polymerization of acrylic acid

In this study, the surface characteristics of polyester and polyamide fabrics were changed by plasma polymerization technique utilizing acrylic acid as precursor. This monomer was used to produce hydrophilic materials with extended absorbency. The hydrophilicity, total wrinkle recovery angle (WRA°) and breaking strength of the fabrics were determined prior and after plasma polymerization treatment. The modification of surfaces was carried out at low pressure (<100 Pa) and low temperature (<50°C) plasma conditions. The effects of exposure time and discharge power parameters were optimized by comparing properties of the fabrics before and after plasma polymerization treatments. It was shown that two sides of polyester fabric samples were treated equally and homogeneously in plasma reactor. For polyester fabrics, the minimum wetting time, 0.5 s, was observed at two plasma processing parameters of 10 W–45 min and 10 W–20 min, where untreated fabric has a wetting time of 6 s. For polyester fabrics, the maximum value was obtained at 60 W–5 min with the wrinkle recovery angle of 306° where the untreated fabric has 290°. The optimum plasma conditions for polyamide fabrics were determined as 30 W–45 min where 2 s wetting time was observed. Wrinkle recovery angle of untreated polyamide fabric was 264°. In this study, after plasma polymerization of acrylic acid, wrinkle recovery angle values were increased by 13%. No significant change was observed in breaking strength of both fabrics after plasma treatment. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 2318–2322, 2007     

Synthesis,characterization, thermal stability,conductivity, and band gap of a new aromatic polyether containing an azomethine as a side

In this study, the oxidative polycondensation reaction conditions of 4‐[(4‐methylphenyl)iminomethyl]phenol (4‐MPIMP) were studied by using oxidants such as air O₂, H₂O₂, and NaOCl in an aqueous alkaline medium between 50 and 90°C. The structures of the synthesized monomer and polymer were confirmed by FTIR, UV–vis, ¹H–¹³C‐NMR, and elemental analysis. The characterization was made by TGA‐DTA, size exclusion chromatography (SEC), and solubility tests. At the optimum reaction conditions, the yield of poly‐4‐[(4‐methylphenyl)iminomethyl]phenol (P‐4‐MPIMP) was found to be 28% for air O₂ oxidant, 42% for H₂O₂ oxidant, and 62% for NaOCl oxidant. According to the SEC analysis, the number–average molecular weight (M_n), weight–average molecular weight (M_w), and polydispersity index values of P‐4‐MPIMP were found to be 4400 g mol^?1, 5100 g mol^?1, and 1.159, using H₂O₂, and 4650 g mol^?1, 5200 g mol^?1, and 1.118, using air O₂, and 5100 g mol^?1, 5900 g mol^?1, and 1.157, using NaOCl, respectively. According to TG analysis, the weight losses of 4‐MPIMP and P‐4‐MPIMP were found to be 85.37% and 72.19% at 1000°C, respectively. P‐4‐MPIMP showed higher stability against thermal decomposition. Also, electrical conductivity of the P‐4‐MPIMP was measured, showing that the polymer is a typical semiconductor. The highest occupied molecular orbital and the lowest unoccupied molecular orbital energy levels and electrochemical energy gaps (E) of 4‐MPIMP and P‐4‐MPIMP were found to be ?5.76, ?5.19; ?3.00, ?3.24; 2.76 and 1.95 eV, respectively. According to UV–vis measurements, optical band gaps (E_g) of 4‐MPIMP and P‐4‐MPIMP were found to be 3.34 and 2.82 eV, respectively. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Fluorescence and photon transmission techniques for studying film formation from PS/GO nanocomposites

Polymer Bulletin - Steady-state fluorescence and UV–Vis techniques were used to study the film formation behavior of composites consisting of pyrene (P)-labeled polystyrene (PS) latex and...     

Effects of reactive and nonreactive POSS types on the mechanical,thermal, and morphological properties of plasticized poly(lactic acid)

The aim of this study is to investigate the effects of the reactive and nonreactive polyhedral oligomeric silsesquioxane (POSSs) types and their composition on the mechanical, thermal, and morphological properties of poly(ethylene glycol) plasticized poly(lactic acid) (PLA) composites prepared with melt compounding. The results showed that the incorporation of POSS decreased the melt viscosity of the compounds regardless of POSS type. The lowest viscosity was obtained with epoxy‐POSS, which is the only one that is liquid at processing temperature in comparison to the others. It was revealed from the mechanical tests that the toughness‐related properties such as impact strength and elongation at break improved by the addition of POSS without remarkable deterioration in stiffness. The chemical structure of the POSS influenced the level of dispersion and hence the mechanical performance of the composites. Octaisobutyl‐POSS, being the nonreactive and nonpolar one, had the best dispersion among the other reactive and polar POSS types. The glass transition temperature of the matrix decreased in the presence of POSS types. In addition, the POSS particles also had an impact on the crystallization of PLA. The thermal stability of the composites improved in the presence of POSS particles with respect to the POSS content and the POSS type. POLYM. ENG. SCI., 54:264–275, 2014. © 2013 Society of Plastics Engineers     

Photoinduced electron transfer mechanism between green fluorescent protein molecules and metal oxide nanoparticles

Green fluorescent protein (GFP) molecules are attached to titanium dioxide and cadmium oxide nanoparticles via sol–gel method and fluorescence dynamics of such a protein–metal oxide assembly is investigated with a conventional time correlated single photon counting technique. As compared to free fluorescent protein molecules, time-resolved experiments show that the fluorescence lifetime of GFP molecules bound to these metal oxide nanoparticles gets shortened dramatically. Such a decrease in the lifetime is measured to be 22 and 43 percent for cadmium oxide and titanium dioxide respectively, which is due to photoinduced electron transfer mechanism caused by the interaction of GFP molecules (donor) and metal oxide nanoparticles (acceptor). Our results yield electron transfer rates of 3.139×10⁸ s⁻¹ and 1.182×10⁸ s⁻¹ from the GFP molecules to titanium dioxide and cadmium oxide nanoparticles, respectively. The electron transfer rates show a marked decrease with increasing driving force energy. This effect represents a clear example of the Marcus inverted region electron transfer process.     

Using Circular Conduits in Ozone Injection

Dissolved oxygen is the amount of oxygen dissolved in water corresponding to an important water quality parameter in rivers, streams, and lakes. Hydraulic structures can increase dissolved oxygen levels by creating turbulent conditions where small air bubbles are carried into the bulk of the flow. A gated conduit is a hydraulic structure that can be used efficiently in aeration and oxygen transfer. The subatmospheric pressure between the upstream and downstream of the gate is the reason for the air injection. Ozone is an unstable gas comprised of three oxygen atoms, and it can be used for water treatment. Ozone is thermodynamically unstable and spontaneously reverts back into oxygen. Ozone has been widely accepted as an effective disinfectant and a chemical oxidant. In this study a series of experiments was conducted to determine the ozone injection performance of circular conduits. Results showed that circular conduits are very effective for ozone injection.     

Hemp seed oil: Minor components and oil quality

Owing to its high content of omega‐6/omega‐3 fatty acids and bioactive minor components with antioxidant activities, hemp seed oil is now recognized for its health benefits by a large number of consumers. This paper primarily discusses the profile of minor components in hemp seed oil and their beneficial and adverse effects on oil quality. While tocopherols, polyphenols and phytosterols prevent oxidative deterioration of hemp seed oil, the high amount of chlorophyll can be detrimental to oil quality.     

Phenolic profiles of Turkish olives and olive oils

Phenolic compound distribution of Turkish olive cultivars and their matching olive oils together with the influence of growing region were investigated. One hundred and one samples of olives from 18 cultivars were collected during two crop years from west, south and south‐east regions of Turkey. The olives were processed to oils and both olive and olive oil samples were evaluated for their phenolic compound distribution. The results have shown that main phenolics of Turkish olives were tyrosol, oleuropein, p‐coumaric acid, verbascoside, luteolin 7‐O‐glucoside, rutin, trans cinnamic acid, luteolin, apigenin, cyanidin 3‐O‐glucoside and cyanidin 3‐O‐rutinoside. Oleuropein and trans cinnamic acid were present in higher amounts among all phenolics. Principal component analyses showed that the growing region did not have drastic effect on phenolic profile of olives. The major phenolic compounds of olive oils were tyrosol, syringic acid, p‐coumaric acid, luteolin‐7‐O‐glucoside, trans cinnamic acid, luteolin and apigenin. Luteolin is a predominant phenolic compound in almost all oil samples. Total phenol concentrations of Southeast Anatolian oils were found to be lower than those of the other regions.