Electrical,mechanical, structural,and thermal behaviors of polymeric gel electrolyte membranes of poly(vinylidene fluoride‐co‐hexafluoropropylene) with the ionic liquid 1‐butyl‐3‐methylimidazolium tetrafluoroborate plus lithium tetrafluoroborate

Polymeric gel electrolyte membranes based on the polymer poly(vinylidene fluoride‐co‐hexafluoropropylene) [P(VdF–HFP)] with different weight percentages of the ionic liquid (IL) 1‐butyl‐3‐methylimidazolium tetrafluoroborate plus 0.3M lithium tetrafluoroborate (LiBF₄) salt were prepared and characterized by scanning electron microscopy, X‐ray diffraction, differential scanning calorimetry, thermogravimetric analysis, Fourier transform infrared (FTIR) spectroscopy, complex impedance spectroscopy, pulse echo techniques, and Vickers hardness (H) testing. After the incorporation of the IL plus the salt solution in the P(VdF–HFP) polymer, the melting temperature, glass‐transition temperature (T_g), degree of crystallinity, thermal stability, elastic modulus (E), and hardness (H) gradually decreased with increasing content of the IL–salt solution as a result of complexation between the P(VdF–HFP) and IL. This was confirmed by FTIR spectroscopy. A part of the IL and LiBF₄ were found to remain uncomplexed as well. The ionic conductivity (σ) of the polymeric gel membranes was found to increase with increasing concentration of the IL–salt solution. The temperature‐dependent σs of these polymeric gel membranes followed an Arrhenius‐type thermally activated behavior. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41456.     

Synthesis of Chlorinated and Non-chlorinated Polyols from Model Cross-Metathesis Modified Triacylglycerols

Three pure triacylglycerols (TAG) containing decenoic acid (D), and stearic acid (S), were hydroxylated into chlorinated and non-chlorinated polyols and studied in detail. D is a fatty moiety that can result from the cross metathesis of small olefins with common vegetable oils such as soybean oil. A fundamental understanding relating chemical composition and derived structure, particularly the number and position of the hydroxyl groups, to physical properties was established allowing us to add some perspective to the growing body of knowledge on industrially relevant polyol and polyurethane systems produced with metathesis-modified TAG (MTAG). The hydroxyl value, crystallization and melting behaviors, thermal degradation behavior of the polyols were directly related to their peculiar shortened and primary functionality inherited from the parent MTAG. The effect of regiochemistry on the physical properties of the polyols was investigated with the chromatography fractions of the trichlorinated polyol of propane-1,2,3-triyl tris(dec-9-enoate), giving an unhindered insight into the role of short and terminal functionality of MTAG polyols that will help select the optimal isomer composition for designer polyurethane materials.     

Crystalline selenite substituted carbonated hydroxyapatite nanorods: Synthesis,characterization, evaluation of bioactivity and cytotoxicity

Synthesis of pure and selenite substituted hydroxyapatites (HAP and Se‐HAP with 0.02–0.10 Se) by sol–gel method and evaluation of their morphological features, nature of functional groups, phase purity, in vitro bioactivity and cytotoxicity are addressed. Spectral studies confirm the incorporation of selenite into the HAP lattice, accompanied by an increase in CO₃^2? content to maintain the charge imbalance following replacement of P⁵⁺ with Se⁴⁺, thus making the formation of selenite substituted carbonated HAP. Selenite substitution in the HAP lattice has led to a higher crystallinity and increased the crystallite size. The morphology of HAP is changed from sphere to rod‐like structure upon substitution by selenite and the size of the rod is increased with an increase in the selenite content. Among the Se‐HAPs, a better in vitro bioactivity and cell viability are observed for 0.02 Se‐HAP and 0.04 Se‐HAP while the trend is reversed when the extent of selenite substitution becomes higher.     

Parameters Influencing Third‐Phase Formation in the Extraction of Th(NO3)4 by some Trialkyl Phosphates

Third‐phase formation in the extraction of Th(IV) by trialkyl phosphates (TalP) such as tri‐n‐butyl phosphate (TBP), tri‐iso‐butyl phosphate (TiBP), tri‐sec‐butyl phosphate (TsBP), tri‐n‐amyl phosphate (TAP), tri‐2‐methylbutyl phosphate (T2MBP), tri‐iso‐amyl phosphate (TiAP), tri‐sec‐amyl phosphate (TsAP), and tri‐cyclo‐amyl phosphate (TcyAP) has been investigated under various conditions. Formation of a third phase in the extraction of Th(IV) by TBP/n‐dodecane as a function of TBP concentration at 303 K was studied. Measurements were also carried out on the extraction of Th(IV) from its solution with near‐zero free acidity by various phosphate/diluent binary solutions (1.1 M) as a function of temperature. Third‐phase formation in the extraction of Th(IV) by 1.1 M TalP in various diluents from nitric acid media has also been studied as a function of equilibrium aqueous‐phase acidity at 303 K. Empirical equations to predict limiting organic concentration with respect to various parameters for third‐phase formation in the extraction of Th(IV) by TBP and TAP from nitric acid media have been derived. Some of the above phosphates have been investigated for the distribution of Th(NO₃)₄ between the “diluent‐rich phase” (DP) and “third‐phase” (TP) in the extraction of Th(IV) by 1.1 M TalP in various diluents from its saturated solution with near‐zero free acidity at 303 K. Results of the above studies are presented in this paper. Based on these studies, the effects of extractant concentration, the temperature, the nature of the diluent, the equilibrium aqueous‐phase acidity, and the structure of the extractant on third‐phase formation behavior of trialkyl phosphates are described in this paper.     

Seasonal Influence on Vapor-and Particle-Phase Polycyclic Aromatic Hydrocarbon Concentrations in School Communities Located in Southern California

Ambient concentrations of 15 vapor-and particle-phase (PM _2.5 ) polycyclic aromatic hydrocarbons (PAHs), listed by the US EPA as priority pollutants, were measured between July 2002 and November 2003 in six Southern California communities participating in a multi-year chronic respiratory health study of schoolchildren. The communities were geographically distributed over two hundred kilometers, extending from Long Beach in coastal Los Angeles, to high mountain areas to the north and west of the Los Angeles basin, and south into Eastern San Diego County. Seasonal and spatial variation in the atmospheric concentrations of PAHs is of interest because this class of compounds includes potent mutagens, carcinogens, and species capable of generating reactive oxygen species (ROS) that may lead to oxidative stress. Naphthalene accounted for 95% of the total PAH mass; annual averages ranged from 89 to 142 ng m ^{? 3} . Benzo[ghi]perylene (BGP) and the pro-carcinogen benzo[a]pyrene (BAP), present almost exclusively in the particle-phase, ranged respectively from 38 to 231 pg m ^?3 and 75 and 111 pg m ^{? 3} , with the highest values observed in Long Beach, a community with a high volume of seaport-related activities, and Lancaster, a commuter dormitory community. A considerable increase in the particle-phase PAH concentration, relative to the vapor-phase, was observed as ambient temperature decreased. Cold/hot season ratios for PAHs in PM _2.5 averaged 5.7, reaching 54 at Long Beach. The presented data underscore the importance of seasonal variations on atmospheric PAH concentrations. These observations are relevant to future interpretation and analysis of community-scale human health effects research.     

Analysis of Scanning DMA Transfer Functions

A new approach to determine transfer functions of scanning differential mobility analyzers (DMAs) is introduced. An expression for non-diffusive particle trajectories in a cylindrical DMA operating in a scanning voltage mode is obtained analytically. Particle trajectory simulations are then used to determine the scanning DMA transfer functions. The results suggest that the shape of the scanning DMA transfer functions may vary with mobility for scan times smaller than a certain value, which depends on the DMA flowrates, and this provides one criteria limiting the fastest scan possible with the conventional DMAs. A simple approach to determine upscan scanning DMA transfer functions in near real-time with minimal number of simulations is described. For upscan operation, the choice of the scantime is seen to impose upper and lower limits on the particle mobility range classified by a scanning DMA. The predicted effect of voltage scanning on altering DMA transfer functions is validated with fast scan experiments.     

Theoretical Modeling of Filtration by Nonuniform Fibrous Filters

Modeling commercial filter media using classical theories results in incorrect filter pressure drop and efficiencies and this is attributed to media inhomogeneity. The use of an arbitrary inhomogeneity factor is seen to be inadequate in accounting for the effect of operating conditions on the performance of inhomogeneous filter media. A simplistic theoretical modeling approach is described here to account for the variations in filter packing densities and to estimate their effect on the media particle capture characteristics. The theoretical modeling results are used in obtaining an equivalent filter packing density distribution from media local efficiency measurements. Considering this variation in the theoretical models is seen to result in better prediction of media performance over a wide range of operating conditions. The observed deviation of experimental efficiencies from the theory at smaller Peclet numbers can be explained from the results of the theoretical analysis.     

Novel Aerosol/Gas Inlet for Aircraft-Based Measurements

A novel inlet has been designed for selective sampling of gas and aerosol phases of volatile species from high-speed aircraft. A multistage flow system brings the flow nearly isokinetically towards the sampling port. Two small airfoil-shaped "blades" are placed close to the sample port to provide the flow conditions required for aerosol and gas sampling. Aerosols are sampled when these blades are positioned to operate the inlet as a counterflow virtual impactor (CVI). The design enables sampling of particles as small as 0.1 w m from a high-speed aircraft under stratospheric conditions, a substantial improvement over that possible with previous CVI designs. For gas sampling, one of the blades is moved by a stepper motor to occlude the inlet opening and gas is sampled perpendicular to the bulk flow. Boundary layer suction is used to prevent the sampled gas from coming in contact with the impactor walls. This is one of the first designs of an inlet that enables gas sampling free of wall contact. The inlet was flown on the NASA ER-2 aircraft during the SOLVE 2000 campaign to study aerosol/gas partitioning of nitric acid in the lower stratosphere. Data from the flight tests show that the inlet flow characteristics are broadly in agreement with computational fluid dynamics (CFD) simulations.     

Effect of dual reinforced ceramic particles on high temperature tribological properties of aluminum composites

The nature and distribution of hard ceramic particles in composite materials influences the properties to greater extent. In the present work, the role of hard ceramic reinforced particles on the tribological behaviour of aluminum metal matrix composites consisting of single (SRP) and dual reinforced particles (DRP) is studied at different temperatures. Zircon sand and silicon carbide particles of size 20–32 μm were used as reinforcement in commercial grade LM13 piston alloy. Composites of dual reinforced particles in aluminum matrix (DRP-AMCs) were developed by mixing 15 wt% reinforced particles by two step stir casting technique. The wear behaviour of DRP-AMCs and SRP-AMCs (single reinforced particles aluminum matrix composite) was investigated using a pin-on-disc method at high temperatures under dry sliding condition. The microstructural examination of developed composites shows globular and finely distributed eutectic silicon in the vicinity of the reinforced particles. Metallographic investigation revealed that the wear zone of the SRP composite consisted of a hardened layer, which is responsible for high wear loss observed in the SRP composite. The results further indicate a transition in the wear mode that occurs after 150 °C for all composites. Study reveals that the dual reinforcement of particles enhances the wear resistance as compared to single reinforced particles if mixed in a definite ratio. A combination of 3% zircon sand and 12% silicon carbide particle reinforced composite exhibits better wear resistance as compared to other combinations at all the temperatures for low and high loads both.     

Development of HDPE/EPDM‐g‐TMEVS nanocomposites with enhanced electrical and flame properties

Nanoclay reinforced HDPE/silane grafted EPDM composites have been developed using an epoxy functionalized HDPE as compatibilizer.The nanoclay has been varied from 0% to 10% in the composites along with the incorporation of compatibilizer and without compatibilizer in a brabender plasticorder.The dielectric and fire retardant properties of these nanocomposites have been examined. Addition of nanoclay enhanced char formation with increased values of limiting oxygen index. Electrical properties such as volume and surface Resistivity improved with addition of nanoclay and compatibilizer. The values of tan δ increased with increase in grafted EPDM and silanated nanoclay loading. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013