Experimental investigation of gasoline fumigation in a single cylinder direct injection (DI) diesel engine

In the presented study, the effects of gasoline fumigation have been investigated experimentally in a single cylinder direct injection (DI) diesel engine. Gasoline has been introduced into the inlet air flow using an elementary carburetor and no other modification on the engine has been done. The effects of 2%, 4%, 6%, 8% and 10% (by vol.) gasoline fumigation have been investigated experimentally at the speeds of (900–1600) (rpm) and at the selected compression ratios of (18–23). From the experimental results it is determined that by application of gasoline fumigation effective power output increases at the levels of 4–9%, effective efficiency increases by approximately 1.5–4% and specific fuel consumption decreases by approximately 1.5–4%. It is also determined that 4–6% fumigation ratio range is the most favorable percentage interval of gasoline at the selected compression ratios for this engine. Because cost of gasoline is higher than diesel fuel in Turkey as well as in many of the other countries and the decrease ratio of specific fuel consumption is low, gasoline fumigation is not economic for this engine. In the presented study, heat balance tests have also been performed for 18 and 21 compression ratios. The heat balance has been investigated experimentally in respect of effective power, heat rejected to the cooling water, heat lost through exhaust, and other losses (unaccounted-for losses). Heat lost through exhaust decreases until 4–6% gasoline fumigation ratios and after these fumigation ratios it starts to increase because of increasing exhaust gas temperature. Heat rejected to the cooling water decreases at low fumigation ratios, but at high fumigation ratios it increases. Other losses generally exhibit an increasing tendency at low fumigation ratios.     

Viscoelastic properties of reactive and non‐reactive blends of ethylene‐methyl acrylate copolymers with styrene‐maleic anhydride copolymer

The effects of compatibilizing reactions on the viscoelastic properties and morphology of ethylene‐methyl acrylate copolymers were studied. Potentially reactive blends of styrene‐maleic anhydride copolymer (SMAH) and a terpolymer of ethylene/methyl acrylate/glycidyl methacrylate (E‐MA‐GMA) were compared with a non‐reactive blend of SMAH and an ethylene/methyl acrylate (E‐MA) copolymer with similar rheological properties. Melt mixing was carried out in a batch mixer and in a co‐rotating twin screw extruder. The morphology of the reactive blends showed smaller domain sizes than the non‐reactive blends, and the viscoelastic properties of the blends were very different. The storage and loss moduli and the complex viscosity of the reactive blends were greater than those of non‐reactive blends. The reactive blends had a higher zero shear viscosity, plateau modulus and mean relaxation time than their non‐reactive counterparts, indicating a higher degree of melt elasticity. The melt elasticity was maximum at 25% functionalized ethylene‐methyl acrylate concentration.     

Modification of maleic anhydride–styrene copolymer with noradrenaline by chemical and enzymatic methods

Maleic anhydride copolymer was modified with another biologically active agent, noradrenaline (NA), using both chemical and enzymatic methods. The modification and synthesized products were named as follows: chemical modification, MASTNAc; enzymatic modification, MASTNAe; enzymatically synthesized MASTNA from individual monomers, MASTNAem. Chemical and enzymatic reactions were performed at 70°C and 38°C, respectively. In the chemical reactions azobisisobutyronitrile was used as the initiator. In the enzymatic reactions, an extracellular extract, including an enzyme with peroxidase‐like activity, was used. All the reactions were performed in an organic medium, methyl ethyl ketone. Structural characterization of the copolymer and modified copolymer were carried out by Fourier transform infrared (FTIR) and nuclear magnetic resonance (¹H NMR). FTIR and ¹H NMR spectra confirmed that NA was successfully covalently bound onto the MAST copolymer backbone by both chemical and enzymatic methods. Surface morphology of the samples was studied by scanning electron microscopy. Results obtained indicated that chemical and enzymatic addition of NA to MAST backbone yielded products having quite similar physical and chemical properties. On the other hand, MASTNA‐modified copolymer synthesized by individual monomers appeared to be different in its chemical structure. Furthermore, enzymatic modification and synthesis appeared to provide a good alternative method because it required much milder conditions such as low temperature, and better product qualities: higher solubility in water, higher yield and purity. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Efficient Longitudinal Seismic Fragility Assessment of a Multispan Continuous Steel Bridge on Liquefiable Soils

The increased failure potential of aging U.S. highway bridges and their susceptibility to damage during extreme events necessitates the development of efficient reliability assessment tools to prioritize maintenance and rehabilitation interventions. Reliability communication tools become even more important when considering complex phenomena such as soil liquefaction under seismic hazards. Currently, two approaches are widely used for bridge reliability estimation under soil failure conditions via fragility curves: liquefaction multipliers and full-scale two- or three-dimensional bridge-soil-foundation models. This paper offers a computationally economical yet adequate approach that links nonlinear finite-element models of a three-dimensional bridge system with a two-dimensional soil domain and a one-dimensional set of p-y springs into a coupled bridge-soil-foundation (CBSF) system. A multispan continuous steel girder bridge typical of the central and eastern United States along with heterogeneous liquefiable soil profiles is used within a statistical sampling scheme to illustrate the effects of soil failure and uncertainty propagation on the fragility of CBSF system components. In general, the fragility of rocker bearings, piles, embankment soil, and the probability of unseating increases with liquefaction, while that of commonly monitored components, such as columns, depends on the type of soil overlying the liquefiable sands. This component response dependence on soil failure supports the use of reliability assessment frameworks that are efficient for regional applications by relying on simplified but accepted geotechnical methods to capture complex soil liquefaction effects.     

Optimization of n nc-Si:H and a-SiNx:H layers for their application in nc-Si:H TFT

The n-type doped silicon thin films were deposited by plasma enhanced chemical vapor deposition (PECVD) technique at high and low H₂ dilutions. High H₂ dilution resulted in n⁺ nanocrystalline silicon films (n⁺ nc-Si:H) with the lower resistivity (ρ ∼0.7 Ω cm) compared to that of doped amorphous silicon films (∼900 Ω cm) grown at low H₂ dilution. The change of the lateral ρ of n⁺ nc-Si:H films was measured by reducing the film thickness via gradual reactive ion etching. The ρ values rise below a critical film thickness, indicating the presence of the disordered and less conductive incubation layer. The 45 nm thick n⁺ nc-Si:H films were deposited in the nc-Si:H thin film transistor (TFT) at different RF powers, and the optimum RF power for the lowest resistivity (∼92 Ω cm) and incubation layer was determined. On the other hand, several deposition parameters of PECVD grown amorphous silicon nitride (a-SiN_x:H) thin films were changed to optimize low leakage current through the TFT gate dielectric. Increase in NH₃/SiH₄ gas flow ratio was found to improve the insulating property and to change the optical/structural characteristics of a-SiN_x:H film. Having lowest leakage currents, two a-SiN_x:H films with NH₃/SiH₄ ratios of ∼19 and ∼28 were used as a gate dielectric in nc-Si:H TFTs. The TFT deposited with the NH₃/SiH₄∼19 ratio showed higher device performance than the TFT containing a-SiN_x:H with the NH₃/SiH₄∼28 ratio. This was correlated with the N−H/Si−H bond concentration ratio optimized for the TFT application.     

The effect of controlled atmosphere storage on pickle production from pickling cucumbers cv. ‘Troy’

Fresh pickling cucumbers (cv. Troy) were stored for 30 days at 7°C and 90–95% relative humidity (RH) under different controlled atmosphere (CA) combinations, and samples taken at 0 (i.e., without storage), 10, 20 and 30 days of storage were processed to sweet pickle. At each sampling, physical and chemical analyses were carried out in the fresh pickling cucumbers to determine the changes in the quality with storage time. Besides, physical, chemical and sensory analyses were carried out in the pickles elaborated from the fresh samples taken at the same periods, after keeping at room temperature for 6 months, with the aim of determining CA and storage time effect on the final pickle quality. It was found that storage of cucumbers to be processed to pickle could be possible for less than 10 days at 7°C temperature and 90–95 RH under normal atmosphere (NA). However, physical and chemical analyses showed that storage period of fresh pickling cucumbers could be prolonged up to 30 days under the same storage conditions, if suitable atmosphere combinations are created. Nevertheless, it was concluded that restricting the storage period of fresh pickling cucumbers to 20 days could give better results after processing to pickle. An erratum to this article can be found at     

Poly(ethylene terephthalate)/carbon nanotube composites prepared with chemically treated carbon nanotubes

Surfaces of multiwalled carbon nanotubes (CNT) were functionalized by treatment with strong acid mixture (purification) followed by modification with sodium dodecyl sulfate, poly(ethylene glycol) (PEG), and diglycidyl ether of Bisphenol A (DGEBA). Poly(ethylene terephthalate) (PET)‐based conductive polymer composites were prepared by using these CNT by means of melt mixing with a twin screw extruder. Amount of carboxylic acid groups on the CNT surface increased after acid treatment but decreased with surface modification due to the consumption of these groups during the chemical reactions between the surface modifiers and CNT surface. Fourier transformed infrared spectroscopy (FTIR) and nuclear magnetic resonance analyses of the composites revealed the increase in the interactions between PET and CNT surface after treatment with PEG and DGEBA. Mechanical strength of the composites prepared with modified CNT were higher than that of the untreated CNT‐filled composite owing to the enhanced interactions between PET and CNT. POLYM. ENG. SCI., 2011. © 2011 Society of Plastics Engineers     

Fabrication of SiO2-stacked diamond membranes and their characteristics for microelectromechanical applications

Diamond is a promising microelectromechanical systems (MEMS) material due to its high Young's Modulus and very large thermal conductivity. In this work, ultrananocrystalline diamond was stacked between silicon dioxide to form thermally-stable and robust membranes. These SiO₂-stacked diamond layers were processed into MEMS-compatible membranes. For comparison, membranes composed of only SiO₂ were fabricated as well. The structural characteristics of these membranes are compared and analyzed for membranes of different diameters. Using finite element modeling, the experimental behaviors of SiO₂ and SiO₂-stacked diamond membranes are analyzed.     

Effect of carbon nanotube purification on the electrical and mechanical properties of poly(ethylene terephthalate) composites with carbon nanotubes in low concentration

Surface properties of carbon nanotubes (CNTs) were altered by purification with nitric acid, sulfuric acid, ammonium hydroxide, and hydrogen peroxide. As‐received and purified CNT‐based conductive poly (ethylene terephthalate) composites were prepared with a twin‐screw extruder. The effects of CNT purification on the surface properties of the CNTs and on the morphology and electrical and mechanical properties of CNT‐based composites were investigated. Surface energy measurements showed that the acidic component of the surface energies of the CNTs increased after purification. According to Fourier transform infrared (FTIR) spectroscopy, the purification resulted in the formation of oxygen‐containing functional groups on the surfaces of the CNTs. Electron spectroscopy for chemical analysis results indicate the removal of the metallic catalyst residues and an increase in the oxygen content of the CNT surfaces as a result of the purification procedure. X‐ray diffraction analyses revealed a change in the crystalline structure of the CNTs after purification. All of the composites prepared with the purified CNTs had higher electrical resistivities and tensile and impact strength values than the composites based on the as‐received CNTs because of the functional groups and defect sites formed on the surfaces of the CNTs during purification. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011