Comparison of primary and secondary aminosilance coupling agents in anhuydride-curde epoxy fiberglass composites

Fourier transform infrared spectroscopy (FT-IR) has been utilized to investigate the interfacial chemical bonding at the interfaces of the aminosilanes and the nedic methyl anhydiride cured epoxy matrix in fiber-reinforced composites. It is found that the nedic methyl anhydride can react with γ-aminopropyltriethoxysilane (APS) and N-methylaminoproplytrimethoxysilane (MAPS). In comparing the relative reactivities of two coupling agents to the epoxy resin, the secondary aminosilance has a higher reactivity than the primary aminosilance. An elevated temperature is required for the copolymerization to take place between the silane and the epoxy resin. The results indicate that covalent bonds form at the coupling agents. The molecular structure of the interface in MAPS treated fiberglass reinforced composites is different from that of the APS treated fiber composites. In addition, an accelerated copolymerization initiated by the coupling agent treated surface is also found in the resin interphase which may be important in determining the mechanical properties of the composites.     

Chemical reactions occurring at the interface of epoxy matrix and aminosilane coupling agents in fiber-reinforced composites

The chemical reactions at the interface between an anhydride-cured epoxy resin and an aminosilane treated fiber have been investigated using Fourier transform infrared methods (FT-IR). The results indicate that chemical bonds are formed in the interfacial region between the matrix and the coupling agents. The amount of interfacial bonding depends on the composition and the processing conditions.     

Corrosion of aluminium in the aqueous chemical environment of a loss-of-coolant accident at a nuclear power plant

Aluminium corrosion is a significant concern in the aqueous chemical environment of the reactor containment building following a hypothetical loss-of-coolant accident (LOCA) at a nuclear power plant. Aluminium corrosion may lead to the formation of precipitates that can, in combination with insulation debris, block the recirculation sump screens. This study investigated aluminium corrosion experimentally at both bench and pilot scale under conditions representative of several types of nuclear power plants. Evidence of corrosion was determined using aqueous concentrations measured with inductively-coupled plasma (ICP) spectrometry and surface examinations using scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), X-ray photoelectron spectrometry (XPS), X-ray fluorescence (XRF), and X-ray diffraction (XRD). Corrosion proceeded slowly at pH near 7, but more rapidly at higher pH when the representative pipe insulation material was fibreglass. However, when calcium silicate pipe insulation was introduced into the system, corrosion became insignificant even at pH values near 10. Experimental evidence indicates that the calcium silicate insulation released a significant amount of silicate to the solution. Silicate formed a passivation layer composed of Al₂OSiO₄ with a thickness of more than 10 nm, and this layer effectively inhibited corrosion.     

Ambient particulate matter exhibits direct inhibitory effects on oxidative stress enzymes

A primary mechanistic hypothesis by which ambient air particles have a significant negative impact on human health is via the induction of pulmonary inflammatory responses mediated through the generation of reactive oxygen species (ROS). Development of a biosensor for the assessment of particulate ROS activity would be a significant advance in air pollution monitoring. The objective of this study was to evaluate whether air particulates interact directly with protective enzymes involved in oxidative stress responses. We performed enzyme activity assays on four enzymes involved in oxidative stress responses (Cu/Zn superoxide dismutase, Mn superoxide dismutase, glutathione peroxidase, and glutathione reductase) in the presence of particles of varying toxicities and found distinctive inhibition patterns. On the basis of these findings, we suggest a strategy for an enzyme bioassay that could be used to assess the potential of particles to generate ROS-induced responses.     

Static and Cyclic Fatigue of Alumina at High Temperatures: II, Failure Analysis

Failure mechanisms of an alumina, tested at 1200°C under static and various cyclic loading conditions, were examined. Slow crack growth of a single crack is the dominant mechanism for the failure in specimens under cyclic loading with a short duration of maximum stress at all applied stress levels, as well as at high applied loads for static loading and cyclic loading with a longer hold time at maximum stress. At low stress levels, failure of static loading and cyclic loading with a longer hold time at maximum stress might occur by formation and/or growth of multiple macrocracks. More importantly, for all the given loading conditions. The viscous glassy phase behind the crack tip could have a bridging effect on the crack surfaces. A simplified model for calculating effective stress intensity factor at the crack tip under static and various cyclic loading demonstrated a trend consistent with the stress–life data.     

Shear rates investigation in a scraped surface heat exchanger

The electrodiffusion technique was performed in order to investigate the shear rate on a scraped surface heat exchanger. Microelectrodes were placed inside: the walls of the outer cylinder; the inlet and outlet bowls; the rotor and the blades. Highly viscous Newtonian fluid (Emkarox HV45 solutions) and non-Newtonian model fluid (aqueous solutions of CMC) were used. The electrodiffusion method allowed us to measure wall shear rates. Maximum shear rate was observed at the scraping surface and caused by blades scraping, high shear rate was also measured on the leading edge of the blades. In the other parts of the exchanger, shear rate remained low but the development of Taylor vortices completely modified the scraped surface heat exchangers behaviour inside the surface of the bowls. A dimensionless representation of the friction factor was established for the inner and outer wall surface of the exchanger.     

Spinodal clustering induced dewetting and non-monotonic stabilization of polymer blend films at high nanofiller concentrations

We examine the effects of high fullerene nanoparticle (f-NP) concentrations, ?_f-NP ∼ (10–20) mass% on polystyrene (PS)/polybutadiene (PB) blend thin film stability. Dewetting of the polymer blend around spinodally clustered f-NPs in this high concentration limit leads to a spinodal like dewetting morphology. This is in contrast to our previously observed results on the stabilization effects of f-NPs on PS/PB blend thin films in the intermediate f-NP concentration range of 7–10 mass%, wherein, after saturating the polymer–blend interface, the NPs stabilize the film by segregating to the blend–substrate interface. We determine three regimes of polymer blend film stability as a function of filler concentration: a) ?_f-NP < 7 mass% where preferential segregation of the f-NPs to the polymer–polymer interface leads to macroscopic dewetting, b) ?_f-NP ∼ (7–10) mass% where PS/PB blend films exhibit complete film stability, and c) ?_f-NP ∼ (11–20) mass%, where spinodal clustering of the f-NPs gives rise to polymer–NP phase exclusion and subsequent dewetting.     

The Interaction of Isopenicillin N Synthase with Homologated Substrate Analogues δ‐(L‐α‐Aminoadipoyl)‐L‐homocysteinyl‐D‐Xaa Characterised by Protein Crystallography

Isopenicillin N synthase (IPNS) converts the linear tripeptide δ‐(L ‐α‐aminoadipoyl)‐L ‐cysteinyl‐D ‐valine (ACV) into bicyclic isopenicillin N (IPN) in the central step in the biosynthesis of penicillin and cephalosporin antibiotics. Solution‐phase incubation experiments have shown that IPNS turns over analogues with a diverse range of side chains in the third (valinyl) position of the substrate, but copes less well with changes in the second (cysteinyl) residue. IPNS thus converts the homologated tripeptides δ‐(L ‐α‐aminoadipoyl)‐L ‐homocysteinyl‐D ‐valine (AhCV) and δ‐(L ‐α‐aminoadipoyl)‐L ‐homocysteinyl‐D ‐allylglycine (AhCaG) into monocyclic hydroxy‐lactam products; this suggests that the additional methylene unit in these substrates induces conformational changes that preclude second ring closure after initial lactam formation. To investigate this and solution‐phase results with other tripeptides δ‐(L ‐α‐aminoadipoyl)‐L ‐homocysteinyl‐D ‐Xaa, we have crystallised AhCV and δ‐(L ‐α‐aminoadipoyl)‐L ‐homocysteinyl‐D ‐S‐methylcysteine (AhCmC) with IPNS and solved crystal structures for the resulting complexes. The IPNS:Fe^II:AhCV complex shows diffuse electron density for several regions of the substrate, revealing considerable conformational freedom within the active site. The substrate is more clearly resolved in the IPNS:Fe^II:AhCmC complex, by virtue of thioether coordination to iron. AhCmC occupies two distinct conformations, both distorted relative to the natural substrate ACV, in order to accommodate the extra methylene group in the second residue. Attempts to turn these substrates over within crystalline IPNS using hyperbaric oxygenation give rise to product mixtures.