Preparation,characterization, and some physical properties of polypropylene/poly(methyl acrylate)‐grafted glass wool composites

Polypropylene/poly(methyl acrylate)‐grafted glass wool (PMA‐g‐GW) mixes were prepared. The polymerization process was carried out using potassium persulfate (PPS) and PPS/acetone sodium bisulfite (ASBS) as a redox‐pair initiation system at 60 and 70°C. The effect of using PPS or PPS/ASBS on the grafting percent and conversion percent reveals that the conversion percent values on using PPS as an initiator are higher than those of PPS/ASBS, while in the case of grafting, the inverse is true, that is, using PPS as an initiator gives grafting percent values lower than those that can be obtained using PPS/ASBS. The dielectric properties, thermal diffusivity, specific heat capacity, and thermal conductivity of PP loaded with modified glass wool as a function of different types and concentrations of initiators—used in the grafting polymerization process, namely, PPS and the redox initiating system—were also studied. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 723–732, 2003     

Aluminum-27 and Silicon-29 Magic-Angle Spinning Nuclear Magnetic Resonance Study of the Kaolinite-Mullite Transformation

The ²⁷Al and ²⁹Si magic-angle spinning nuclear magnetic resonance (MAS-NMR) study of the kaolinite-mullite transformation has shown the presence of Al in tetra- and pentacoordination in dehydroxylated kaolinite. The ²⁹Si NMR signal analysis of samples heated above 400°C demonstrates that the tetrahedral sheet of kaolinite begins to break down near 600°C and continues to do so to 900°C. From the ²⁷Al NMR signal evolution, it can be deduced that the exothermic peak at 980°C in DTA curves is associated with the modification of the coordination of Al, which changes from the tetra- or pentacoordination to the more stable octahedral coordination. Heating the sample at 880°C for 36 h produces the same transformation in the coordination of Al ions and the elimination of the exothermic peak at 980°C in the DTA diagram. After this transformation, all spectra show two tetrahedral lines characteristic of mullite, indicating that nuclei of mullite with low crystallinity are generated during the exothermic process which are not detected by XRD. At higher temperatures tetrahedral NMR peaks increase in intensity, yielding, at 1200°C, the 3:2 mullite NMR spectrum.     

The preparation of an amino acid-based surfactant and its potential application as an EOR agent

Most of the synthetic surfactants investigated with the aim of enhanced chemically oil recovery in the literature have environmental drawbacks. In this work, application of an environmentally-friendly synthetic surfactant as an enhanced oil recovery agent is introduced by measuring interfacial tension of water–kerosene systems and wettability alteration of carbonate pellets. For this purpose, an amino acid-based surfactant was initially synthesized using a new synthetic approach which was subsequently confirmed by spectra of Fourier transform infrared and Proton nuclear magnetic resonance. Results showed a value of critical micelle concentration in the range of 9000–9100 ppm for this surfactant. Results also demonstrated a decrease of 38.53% in water–kerosene system interfacial tension and a 17.76% reduction in oil-wetness of the carbonate pellets.     

Modeling of CO2-brine interfacial tension: Application to enhanced oil recovery

Development of reliable and accurate models to estimate carbon dioxide–brine interfacial tension (IFT) is necessary, since its experimental measurement is time-consuming and requires expensive experimental apparatus as well as complicated interpretation procedure. In the current study, feed forward artificial neural network is used for estimation of CO₂–brine IFT based on data from published literature which consists of a number of carbon dioxide–brine interfacial tension data covering broad ranges of temperature, total salinity, mole fractions of impure components and pressure. Trial-and-error method is utilized to optimize the artificial neural network topology in order to enhance its capability of generalization. The results showed that there is good agreement between experimental values and modeling results. Comparison of the empirical correlations with the proposed model suggests that the current model can predict the CO₂–brine IFT more accurately and robustly.     

Road Oriented Traffic Information System for Vehicular Ad hoc Networks

Over the last few years, vehicular ad hoc networks (VANETs) have gained popularity for their interesting applications. To make efficient routing decisions, VANET routing protocols require road traffic density information for which they use density estimation schemes. This paper presents a distributed mechanism for road vehicular density estimation that considers multiple road factors, such as road length and junctions. Extensive simulations are carried out to analyze the effectiveness of the proposed technique. Simulation results suggested that, the proposed technique is more accurate compared to the existing technique. Moreover, it facilitate VANET routing protocols to increase packet delivery ratio and reduce end-to-end delay.     

Infectious properties of human immunodeficiency virus type 1 mutants with distinct affinities for the CD4 receptor

Recent evidence suggests that primary patient isolates of T-cell-tropic human immunodeficiency virus type 1 (HIV-1 ) have lower affinities for CD4 than their laboratory-adapted derivatives, that this may partly result from tighter gp120-gp41 bonds that constrain the CD4 binding sites of the primary viruses, and that selection for increased CD4 affinity may be the principal factor in laboratory adaptation of HIV-1 (S. L. Kozak, E. J. Platt, N. Madani, F. E. Ferro, Jr., K. Peden, and D. Kabat, J. Virol. 71:873-882, 1997). These conclusions were based on studies with a panel of HeLa-CD4 cell clones that differ in CD4 levels over a broad range, with laboratory-adapted viruses infecting all clones with equal efficiencies and primary T-cell-tropic viruses infecting the clones in proportion to cellular CD4 levels. Additionally, all of the primary and laboratory-adapted T-cell-tropic viruses efficiently used CXCR-4 (fusin) as a coreceptor. To test these conclusions by an independent approach, we studied mutations in the laboratory-adapted virus LAV/IIIB that alter the CD)4 binding region of gp120 and specifically reduce CD4 affinities of free gp 120 by 85 to 98% (U. Olshevsky et al., J. Virol. 64:5701-5707, 1990). These mutations reduced virus titers to widely varying extents that ranged from severalfold to several orders of magnitude and converted infectivities on the HeLa-CD4 panel from CD4 independency to a high degree of CD4 dependency that resembled the behavior of primary patient viruses. The relative infectivities of the mutants correlated closely with their sensitivities to inactivation by soluble CD4 but did not correlate with the relative CD4 affinities of their free gp120s. Most of the mutations did not substantially alter envelope glycoprotein synthesis, processing, expression on cell surfaces, incorporation into virions, or rates of gp120 shedding from virions. However, one mutation (D457R) caused a decrease in gp160 processing by approximately 80%. The fact that several mutations increased rates of spontaneous viral inactivation (especially D368P) suggests that HIV-1 life spans may be determined by structural stabilities of viral envelope glycoproteins. All of the wild-type and mutant viruses were only slowly and inefficiently adsorbed onto cultured CD4-positive cells at 37 degrees C, and the gradual declines in viral titers in the media were caused almost exclusively by spontaneous inactivation rather than by adsorption. The extreme inefficiency with which infectious HIV-1 is able to infect cultured susceptible CD4-positive cells in standard assay conditions casts doubt on previous inferences that the vast majority of retrovirions produced in cultures are noninfectious. Apparent infectivity of T-cell-tropic HIV-1 in culture is limited by productive associations with CD4 and is influenced in an interdependent manner by CD4 affinities of viral gp120-gp41 complexes and quantities of cell surface CD4.     

Chemometric Characterization of Eight Monovarietal Algerian Virgin Olive Oils

Differences in triacylglycerol, fatty acid, squalene, and tocopherol compositions were demonstrated between 8 varieties of virgin olive oils (Aberkane, Aguenaou, Aharoun, Aimel, Bouchouk Guergour, Bouichret, Chemlal, and Sigoise) from Petite Kabylie area, north eastern Algeria. Fatty acid and triacylglycerol morphotypes characterized each variety. A principal component analysis, based on triacylglycerol, fatty acid, and squalene compositions, differentiates between varieties. Minor fatty acids and squalene, usually not taken into account individually in authentication studies, are strongly involved in this differentiation, whereas the discriminant power of tocopherols is weak. Soft Independent Modeling of Class Analogy classification using chemical compositions as variables showed a high potential to authenticate the varietal origin of Algerian virgin olive oils.     

PALS free volume study of dry and water saturated epoxies

Free volume cavity sizes and fractions of epoxy specimens were determined using positron annihilation lifetime spectroscopy (PALS). PALS data were obtained before and after specimen water equilibration. Specimens were bisphenol A epoxide (B) and/or glycol epoxide (G) cured with a polyamide. Free volume sites increased linearly and cavity sizes decreased linearly with epoxide B:G ratio. Glass transition temperature (T_g) increased with epoxide B:G ratio. Water molecules in wet epoxy B filled approximately six percent of the cavities. Epoxy G cavity size increased 11.4% after water equilibrium and was ascribed to cavity expansion. PALS results differed for commercial corrosion inhibitors in wet and dry mixtures of these epoxides. Zettlemoyer Center for Surface Studies, 7 Asa Dr., Bethlehem, PA 18015. MAHMOUD M. MADANI is with the Zettlemoyer Center for Surface Studies at Lehigh University. He received his B.S. Degree in Physics from Pars College, Tehran, Iran in 1975; his B.S. Honors in 1981, M.S. Degree in 1982, and his Ph.D. Degree in 1986 from Royal Holloway and Bedford New Colleges, University of London. Dr. Madani’s current research studies include the physical chemical characteristics of polymeric coatings and the reliability and characterization of microelectronic packaging materials using PALS, EIS, XPS, SEM, XRD, and MS. He has developed several computer codes for instrumentation interfaces and data analyses. Previously, he was a lecturer in Physics at the University of Bophutatswana, South Africa. Dr. Madani is author and co-author of more than 20 scientific publications. Dr. Madani is a member of the American Physics Society. ROY R. MIRON is a Visiting Research Scientist at the Zettlemoyer Center for Surface Studies at Lehigh University. He received his B.A. and his Ph.D. Degrees from Lehigh University and his M.S. from Middlebury College. Dr. Miron has a broad background in coatings technology. He is the holder of several patents and his publications have appeared inAnalytical Chemistry, Journal Applied Polymer Science, Plastics Paint and Rubber, Plant Engineering, Western Paint Review, and the Hydrocarbon Processing and Petroleum Refiner. He has held memberships in the American Chemical Society and Society of Plastics Engineers. Dr. Miron has presented papers to the Society of Plastics Industry, Society of Plastics Engineers, and the Liberty Bell Corrosion Course. RICHARD D. GRANATA is Lehigh University Senior Research Scientist and Director of the Corrosion Laboratory. He received B.S. and Ph.D. Degrees from The American University in Washington, D.C., studying electrochemistry with Robert Foley. As a Research Scientist at Carnegie-Mellon Institute of Research with Howard Gerhart, he worked on cathodic electrocoating formulations. Moving to Lehigh University, Dr. Granata joined Henry Leidheiser at the Zettlemoyer Center for Surface Studies and continued research in protective polymers and electrochemical corrosion. He has one patent and over 50 technical papers as the author or co-author. His research experience has been acquired in cooperative work on industry and government sponsored programs. He has acquired a broad perspective on corrosion science and technology through this experience with problems involving electrochemical corrosion mechanisms, surface modification by ion implantation, cathodic delamination mechanism, corrosion inhibition, food container life-predictions, corrosion mechanisms in electronics packaging, and protective mechanisms of polymer coatings. Dr. Granata is a member of the Philadelphia Society for Coatings Technology, ECS, National Association of Corrosion Engineers, American Society for Testing and Materials, Steel Structures Paint Council, and American Chemical Society.