Proton conduction promoted by 1H-1,2,3-benzotriazole in non-humidified polymer membranes

Heterocyclic protogenic solvents are promising candidates in production of proton conductive non-humidified membranes. In this work, 1H-1,2,3-Benzotriazole, BTri which is a novel protogenic solvent was incorporated into Nafion and polyvinylphosphonic acid, PVPA to produce novel anhydrous membranes. The composite membranes were characterized using FTIR, TGA and DSC. TGA results confirmed the thermal stability of the membranes and DSC results verified the homogeneity of the materials. The proton conductivity of these polymer electrolyte membranes with respect to BTri content was investigated. 1H-1,2,3-Benzotriazole promoted the proton conductivity of the membranes reaching approximately 10⁻³ S/cm at 150 °C, under anhydrous conditions. Cyclic voltammetry (CV) results demonstrated that 1H-1,2,3-benzotriazole has broad electrochemical stability domain.     

The impact of anthropogenic and biogenic emissions on surface ozone concentrations in Istanbul

Surface ozone concentrations at Istanbul during a summer episode in June 2008 were simulated using a high resolution and urban scale modeling system coupling MM5 and CMAQ models with a recently developed anthropogenic emission inventory for the region. Two sets of base runs were performed in order to investigate for the first time the impact of biogenic emissions on ozone concentrations in the Greater Istanbul Area (GIA). The first simulation was performed using only the anthropogenic emissions whereas the second simulation was performed using both anthropogenic and biogenic emissions. Biogenic NMVOC emissions were comparable with anthropogenic NMVOC emissions in terms of magnitude. The inclusion of biogenic emissions significantly improved the performance of the model, particularly in reproducing the low night time values as well as the temporal variation of ozone concentrations. Terpene emissions contributed significantly to the destruction of the ozone during nighttime. Biogenic NMVOCs emissions enhanced ozone concentrations in the downwind regions of GIA up to 25 ppb. The VOC/NO_x ratio almost doubled due to the addition of biogenic NMVOCs. Anthropogenic NO_x and NMVOCs were perturbed by ± 30% in another set of simulations to quantify the sensitivity of ozone concentrations to the precursor emissions in the region. The sensitivity runs, as along with the model-calculated ozone-to-reactive nitrogen ratios, pointed NO_x-sensitive chemistry, particularly in the downwind areas. On the other hand, urban parts of the city responded more to changes in NO_x due to very high anthropogenic emissions.     

Effects of multipurpose contact lens solutions on the protein composition of the tear film.

OBJECTIVES: To analyze the influence of multipurpose contact lens cleaning solutions on tear proteins. Changes in tear film protein profiles of contact lens wearers who used several marketed brands of multipurpose contact lens care solutions, were assessed by ProteinChip analysis. METHODS: Three studies were conducted. Study I was a comparison of Complete and OptiFree multipurpose solutions. Study II was a study with Complete Moisture Plus solution, Study II was a comparison of Renu and Solocare contact lens solutions. Wearers of soft contact lenses were assigned to use the contact lens care solutions for 4 weeks. Non-contact lens wearing patients were used as controls. Tear samples of each participant were analyzed with the ProteinChip (SELDI-TOF) system. Multivariate statistical analysis and artificial neural networks were used to determine the tear protein profiles of each study group. RESULTS: Before starting the use of the solutions, the tear protein composition in all contact lens wearers deviated from the tear composition of the non-contact lens wearing controls. After 4 weeks of using the different care regimens, the tear protein composition of the patients using Complete or Complete Moisture Plus solutions tended to move toward that of the non-contact lens wearing controls. The tear protein composition of patients using the OptiFree, Renu or Solocare solutions did not undergo a measureable change in the protein level. CONCLUSIONS: The ProteinChip system can analyze protein profiles for large-scale applications as in clinical studies. Two multipurpose solutions, Complete and Complete Moisture Plus, demonstrated a beneficial effect on the tear proteins in contact lens wearers.     

Proton‐conducting blend membranes of crosslinked poly(vinyl alcohol)–sulfosuccinic acid ester and poly(1‐vinyl‐1,2,4‐triazole) for high temperature fuel cells

New type of composite membranes were synthesized by crosslinking of poly(vinyl alcohol) (PVA) with sulfosuccinic acid (SSA) and intercalating poly(1‐vinyl‐1,2,4‐triazole) (PVTri) into the resulting matrix. The complexed structure of the membranes was confirmed by Fourier transform infrared (FTIR) spectroscopy. The resulting hybrid membranes were transparent, flexible, and showed good thermal stability up to ～200°C. The proton conductivities of the membranes were investigated as a function of PVTri and SSA and operating temperature. The water/methanol uptake was measured and the results showed that solvent absorption of the materials increased with increasing PVTri content in the matrix. The proton conductivity of the membranes continuously increased with increasing SO₃H content, PVTri content, and the temperature. In the anhydrous state, the maximum proton conductivity is 7.7 × 10^?5 S/cm for PVA–SSA–PVTri‐1 and for PVA–SSA–PVTri‐3 is 1.6 × 10^?5 S/cm at 150°C. After humidification (RH = 100%), PVA–SSA–PVTri‐4 showed a maximum proton conductivity of 0.0028 S/cm at 60°C. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Optimization of mobile phase in the separation of beta-blockers by HPLC

Beta-blockers are generally determined using high-performance liquid chromatography (HPLC). Previous HPLC separations of beta-blockers have often required a mobile phase containing three components; acetonitrile or methanol to control the retention; buffer to control the ionic strength and pH of the mobile phase; ion-pairing reagent to provide adequate retention of beta-blockers or organic amines as masking agent to reduce peak tailing. Due to the complexity of the mobile phases employed, development of these assays can be a laborious process. Additionally, alkyl sulphonates and organic amines dramatically reduces the life-time reduction of silica based C18 columns. The results of this study demonstrated that the addition of tested alkyl sulphonates and organic amines is not essential for an adequate separation of beta-blockers. In this study, we developed a simple HPLC method for the simultaneous separation of model beta-blockers, atenolol, practolol, metoprolol, oxprenolol and propranolol. Atenolol, practolol, metoprolol, oxprenolol and propranolol adequately separated with high peak symmetries using a mobile phase consisted of methanol/acetonitrile/phosphate buffer (10 mM, pH 3.0) (15:15:70, v/v/v). By altering only the fraction of methanol with respect to acetonitrile, method development becomes a more efficient separation. Furthermore, atenolol, practolol, metoprolol, oxprenolol and propranolol can be detected up to 0.25, 5, 10, 50 and 10 ng ml(-1). In this publication, we present the simultaneous separation of beta-blockers having a wide range of polarity. It is proposed that this new mobile phase, consisting only acetonitrile, methanol and phosphate buffer can be used for the analysis of the several beta-blockers presently in doping control analysis as well as others.     

Performance comparison of state-of-the-art heterojunction bipolar devices (HBT) based on AlGaAs/GaAs, Si/SiGe and InGaAs/InP

This paper presents a comprehensive comparison of three state-of-the-art heterojunction bipolar transistors (HBTs); the AlGaAs/GaAs HBT, the Si/SiGe HBT and the InGaAs/InP HBT. Our aim in this paper is to find the potentials and limitations of these devices and analyze them under common Figure of Merit (FOM) definitions as well as to make a meaningful comparison which is necessary for a technology choice especially in RF-circuit and system level applications such as power amplifier, low noise amplifier circuits and transceiver/receiver systems. Simulation of an HBT device with an HBT model instead of traditional BJT models is also presented for the AlGaAs/GaAs HBT. To the best of our knowledge, this work covers the most extensive FOM analysis for these devices such as I-V behavior, stability, power gain analysis, characteristic frequencies and minimum noise figure. DC and bias point simulations of the devices are performed using Agilent's ADS design tool and a comparison is given for a wide range of FOM specifications. Based on our literature survey and simulation results, we have concluded that GaAs based HBTs are suitable for high-power applications due to their high-breakdown voltages, SiGe based HBTs are promising for low noise applications due to their low noise figures and InP will be the choice if very high-data rates is of primary importance since InP based HBT transistors have superior material properties leading to Terahertz frequency operation.     

Intrinsically proton-conducting poly(1-vinyl-1,2,4-triazole)/triflic acid blends

In the present work, proton conductivity in a polymer blend comprising proton solvating heterocycles was examined. Poly(1-vinyl-1,2,4-triazole), PVTri was produced by free radical polymerization of 1-vinyl-1,2,4-triazole and then proton-conducting polymer electrolytes were obtained by blending of PVTri with trifluoromethanesulfonic acid, triflic acid (TA). To promote the intrinsic proton conductivity the percent blending ratio was changed from 25% to 150% with respect to polymer repeat unit. The protonation of aromatic heterocyclic rings was proved with Fourier-transform infrared spectroscopy (FT-IR). Thermogravimetry (TG) analysis showed that the samples are thermally stable up to approximately 300 °C. Differential scanning calorimetry (DSC) results illustrated that the samples are homogeneous and their glass transition temperatures are located within 130-160 °C. The surface morphology of the materials were characterized by scanning electron microscopy (SEM). The proton conductivity of the blends increased with triflic acid concentration and the temperature. In the anhydrous state, the proton conductivity of PVTriTA100 is 2.2 × 10⁻⁴ S/cm at 150 °C and that of PVTriTA150 is approximately 0.012 S/cm at 80 °C which is similar to that of hydrated Nafion^®.     

The effects of intranasal midazolam on urodynamic studies in children

OBJECTIVE: To determine the influence of midazolam on the function of the lower urinary tract when used to sedate the patient. PATIENTS AND METHODS: Urodynamic studies were performed on 20 patients (seven boys and 13 girls, mean age 4.04 years, range 1 day to 10 years) before and after the intranasal administration of 0.5 mg/kg of midazolam. The patients' heart rate, respiratory rate and oxygen saturation were monitored and the level of sedation recorded by an anaesthesiologist and a surgeon during the study. RESULTS: Heart rate and respiratory rate did not change and the percentage oxygen saturation remained stable throughout the study period. The childrens' behaviour began to change 3-5 min after the intranasal administration of midazolam. The sedation lasted 2 h and the full co-operation of the patient was assured. The difference between the initial and post-midazolam evaluation of maximal cystometric capacity, contractility, compliance, intravesical pressure, maximum flow rate, intravesical pressure at maximum flow and the amount of residual urine were statistically insignificant (P > 0.05). Electromyographic characteristics showed no significant change with the use of midazolam (P > 0.05). CONCLUSION: Despite the suggestion that benzodiazepines, especially diazepam, are useful for the relaxation of pelvic floor striated musculature in voiding dysfunctions, there was no effect on urodynamic variables when midazolam was used in a single dose intranasally. The anxiolytic and sedative effects allowed children to undergo urodynamic studies in comfort.     

MAC Protocols for Energy Harvesting Wireless Sensor Networks: Survey

Energy harvesting (EH) technology in the field of wireless sensor networks (WSNs) is gaining increasing popularity through removing the burden of having to replace/recharge depleted energy sources by energy harvester devices. EH provides an alternative source of energy from the surrounding environment; therefore, by exploiting the EH process, WSNs can achieve a perpetual lifetime. In view of this, emphasis is being placed on the design of new medium access control (MAC) protocols that aim to maximize the lifetime of WSNs by using the maximum possible amount of harvested energy instead of saving any residual energy, given that the rate of energy harvested is greater than that which is consumed. Various MAC protocols with the objective of exploiting ambient energy have been proposed for energy‐harvesting WSNs (EH‐WSNs). In this paper, first, the fundamental properties of EH‐WSN architecture are outlined. Then, several MAC protocols proposed for EH‐WSNs are presented, describing their operating principles and underlying features. To give an insight into future research directions, open research issues (key ideas) with respect to design trade‐offs are discussed at the end of this paper.     

Synthesis and proton conductivity studies of methacrylate/methacrylamide‐based azole functional novel polymer electrolytes

Anhydrous polymer electrolytes based on azole functional methacrylates and methacrylamides have been produced for use in proton exchange membrane fuel cells (PEMFCs). Poly(methacryloyl chloride) (PMAC) was prepared first by free‐radical polymerization of methacryloyl chloride, followed by side chain functionalization with 5‐aminotetrazole (ATet), 3‐amino‐1,2,4‐triazole (ATri) and 1H‐1,2,4‐triazole (Tri). Finally, the obtained polymers were doped with triflic acid (TA) at stoichometric ratios of 1.0, 2.0 and 4.0 with respect to azole units, and the anhydrous polymer electrolytes were obtained. The membranes were characterized by FT‐IR, ¹³C‐NMR, and elemental analysis. Thermal behaviour of polymers was explored by TGA and DSC. The samples were thermally stable up to approximately 200 ^oC. Proton conductivity was measured by impedance spectroscopy. Trifilic acid doped poly(methacryloyl aminotetrazole) (PMAATet‐(TA)₄), poly(methacryloyl‐3‐amino‐1,2,4‐triazole) (PMA‐Tri‐(TA)₄), and poly(methacryloyl‐1,2,4‐triazole) (PMA‐ATri‐(TA)₄) showed maximum proton conductivities of 0.01 Scm^?1, 0.02 Scm^?1 and 8.7x10^?4 Scm^?1, respectively, at 150^°C and anhydrous conditions. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39915.