Experimental Evaluation of Dynamic Effects for a Selected Highway Bridge

The paper presents an experimental study of the actual dynamic effects for a preselected typical highway bridge. Knowledge of the dynamic impact factors is important for accurate determination of the ultimate load capacity and performance assessment of constructed bridges. Static and dynamic field tests were performed on a two-lane concrete highway bridge built in 1999 on U.S. 90 in northwest Florida. During the tests, one or two fully loaded trucks crossed over the bridge, which was instrumented with strain gauges, accelerometers, and displacement transducers. A wooden plank was placed across the lanes for some runs to trigger extensive dynamic vibration and to simulate poor road surface conditions. Data collected from the tests were used for comprehensive assessment of the bridge under dynamic loading. Impact factors obtained from the tests with higher speeds were found larger than corresponding values recommended by bridge codes. Analysis revealed that stiff vehicle suspension, road surface imperfection, and “bouncing” of the truck loading contributed to the high impact factors. Experimental data were also used for validation of the finite-element models developed for the vehicle–bridge system.     

Electrochemical detection of Cr(VI) with carbon nanotubes decorated with gold nanoparticles

Journal of Applied Electrochemistry - A nanocomposite consisting of gold nanoparticles deposited on the side walls of functionalised multi-walled carbon nanotubes, Ox-MWCNT-Aunano, was prepared...     

Digestion kinetics of leaf,stem and inflorescence from five species of mature grasses

The objective of this study was to measure the digestion kinetics for mature (green and non‐senescent) components of five grass species using in sacco and in vitro incubations to define rates of degradation and nutrient release. Mature perennial ryegrass, tall fescue, Yorkshire fog, phalaris and paspalum were hand separated into leaf blade, stem and inflorescence (flower head) for incubations. Concentrations of neutral detergent fibre (NDF) in fractions were in the ranges 492–677 (leaf), 626–718 (stem) and 501–677 (inflorescence) g kg^?1 dry matter (DM). Crude protein concentrations in the DM of the respective fractions were 70–236 (leaf blade), 35–77 (stem) and 75–120 (inflorescence) g kg^?1 DM. Soluble DM (% of the total) determined after mincing accounted for 31–54% of leaf, 26–56% of stem and 20–49% of inflorescence and fractional degradation of the insoluble DM was very slow, in the ranges 0.04–0.11 (leaf), 0.03–0.05 (stem) and 0.03–0.08 (inflorescence) h^?1. After 24 h of in vitro incubation, plant nitrogen content became limiting for fermentation in most instances, especially with tall fescue and paspalum. Volatile fatty acid (VFA) production appeared to be similar for leaf, stem and flower fractions, but the proportion of plant DM released as VFA after 48 h was only 7–12%, with a higher value (19%) for tall fescue. Nitrogen concentration in forage DM was not directly related to VFA yield in vitro. In conclusion, the in sacco kinetics suggested slow colonisation of all components, but especially stem, which will limit the rate of nutrient production. Effective degradability was highest for leaf but rates in vivo will depend on the speed and extent of particle size reduction by chewing during eating and ruminating. Copyright © 2005 Society of Chemical Industry     

Hydrogenation of a Tri-layer High Performance Elastomer: Substrate Synthesis,Catalytic Latex Hydrogenation,and Catalyst Recovery

A whole set of “green” nano-processes providing hydrogenated PMMA-PS-NBR tri-layer core–shell nanostructured high performance rubbers was developed in this research, which involved the synthesis of diene elastomers as the substrate, followed by the catalytic hydrogenation reaction, and finally catalyst recovery. This study may contribute to the development of hydrogenated high performance elastomers in latex form and recovery of catalyst from the polymer matrix.     

Synthesis of poly(methyl methacrylate) nanoparticles initiated by azobisisobutyronitrile using a differential microemulsion polymerization technique

Nanosized poly(methyl methacrylate) (PMMA) particles with a high molecular weight of 10⁶ g mol^?1 and a polydispersity index of about 1–2 were synthesized, for which 2,2′‐azobisisobutyronitrile was used as the initiator and a differential microemulsion polymerization technique was employed. The kinetics of the polymerization, the glass transition temperature, tacticity, the particle size distribution, and the morphology of the nanosized PMMA synthesized were investigated. The dependence of the number of the polymer particles (N_p) and the number of the micelles (N_m) on the concentration of the surfactant was discussed. The molecular weight distribution was found to be nearly constant over the polymerization time, which was attributed to the significance of micellar polymerization. The resultant nanosized PMMA has a rich syndiotactic configuration (53–57% rr triads) with a glass transition temperature of about 125°C. A beneficial operation condition was discovered where the conversion reached a maximum at a high monomer‐to‐water ratio. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Innovative collagen nano-hydroxyapatite scaffolds offer a highly efficient non-viral gene delivery platform for stem cell-mediated bone formation

The ability of nano-hydroxyapatite (nHA) particles developed in-house to act as non-viral delivery vectors is assessed. These nHA particles are combined with collagen to yield bioactive, biodegradable collagen nano-hydroxyapatite (coll-nHA) scaffolds. Their ability to act as gene-activated matrices for BMP2 delivery is demonstrated with successful transfection of mesenchymal stem cells (MSCs) resulting in high calcium production.     

Photoinduced Degradation of Polymer and Polymer–Fullerene Active Layers: Experiment and Theory

As organic photovoltaic efficiencies steadily improve, understanding degradation pathways becomes increasingly important. In this paper, the stability under prolonged illumination of a prototypical polymer:fullerene active layer is studied without the complications introduced by additional layers and interfaces in complete devices. Combining contactless photoconductivity with spectroscopy, structural characterization at the molecular and film level, and quantum chemical calculations, the mechanism of photoinduced degradation in bulk heterojunctions of poly (3‐hexylthiophene) (P3HT) and [6,6]‐phenyl C61‐butyric acid methyl ester (PCBM) is studied. Bare films are subjected to four conditions for 1000 h with either constant illumination or dark and either ambient or inert atmosphere. All samples are found to be intrinsically stable for 1000+ h under inert conditions, in contrast to complete devices. While PCBM stabilizes P3HT films exposed to air, its fullerene cage is found to undergo a series of oxidations that are responsible for the deterioration of the photoconductivity of the material. Quantum chemical calculations show that PCBM oxides have deeper LUMO levels than pristine PCBM and therefore act as traps for electrons in the PCBM domains.     

A three-phase nonequilibrium dynamic model for catalytic distillation

A detailed three-phase nonequilibrium (NEQ) dynamic model for simulating batch and continuous catalytic distillation (CD) processes has been developed. In this model, both molar and energy holdups in liquid and vapour phases are taken into account. Multicomponent mass transfer and heat transfer between vapour and liquid phases as well as between liquid and solid (catalyst) phases are described by the Maxwell-Stefan equations. The resulting differential and algebra equations in this model are implemented in gPROMS and C++. The simulation results are in good agreement with the experimental data obtained from the batch and continuous CD processes for the production of diacetone alcohol (DAA) using Amberlite IRA-900 as a catalyst. Sensitivity analysis on the mass transfer and kinetics using the three-phase NEQ dynamic model indicates that the formation of DAA is controlled by solid-liquid mass transfer, whereas the formation of mesityl oxide is kinetically controlled under the simulation conditions.     

Application of rice husk ash as fillers in the natural rubber industry

Rice husk ash (RHA) obtained from agricultural waste, by using rice husk as a power source, is mainly composed of silica and carbon black. A two‐stage conventional mixing procedure was used to incorporate rice husk ash into natural rubber. For comparison purposes, two commercial reinforcing fillers, silica and carbon black, were also used. The effect of these fillers on cure characteristics and mechanical properties of natural rubber materials at various loadings, ranging from 0 to 40 phr, was investigated. The results indicated that RHA filler resulted in lower Mooney viscosity and shorter cure time of the natural rubber materials. The incorporation of RHA into natural rubber improved hardness but decreased tensile strength and tear strength. Other properties, such as Young's modulus and abrasion loss, show no significant change. However, RHA is characterized by a better resilience property than that of silica and carbon black. Scanning electron micrographs revealed that the dispersion of RHA filler in the rubber matrix is discontinuous, which in turn generates a weak structure compared with that of carbon black and silica. Overall results indicate that RHA can be used as a cheaper filler for natural rubber materials where improved mechanical properties are not critical. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 34–41, 2005