Novel use of glow discharge optical emission spectroscopy (GDOES) to study corrosion of AA2024‐T3 in the presence and absence of inhibitors – part 3: investigating the effects of various proportions of inhibitor in the coating matrix or in nanocontainers

Elemental depth profiling by glow discharge optical emission spectroscopy has been used to characterize the corrosion products on AA2024‐T3. In previous work, the aluminium, oxygen and copper depth profiles were shown to provide information regarding surface roughening, the thickness of corroded layers and extent of copper de‐alloying/relocation. Nitrogen, sulfur, phosphorus and chromium depth profiles were examined in the hope of detecting inhibitor species within the corroded/altered layers after 5 h of exposure to a corrosive solution. In the present work, the study is extended to longer exposure time. The work presents a further study of the leaching of benzotriazole from the coating matrix or from nanocontainers during various times of exposure to a corrosive environment. Copyright © 2016 John Wiley & Sons, Ltd.     

Observational constraints on multimessenger sources of gravitational waves and high-energy neutrinos

Many astronomical sources of intense bursts of photons are also predicted to be strong emitters of gravitational waves (GWs) and high-energy neutrinos (HENs). Moreover some suspected classes, e.g., choked gamma-ray bursts, may only be identifiable via nonphoton messengers. Here we explore the reach of current and planned experiments to address this question. We derive constraints on the rate of GW and HEN bursts based on independent observations by the initial LIGO and Virgo GW detectors and the partially completed IceCube (40-string) HEN detector. We then estimate the reach of joint GW+HEN searches using advanced GW detectors and the completed km(3) IceCube detector to probe the joint parameter space. We show that searches undertaken by advanced detectors will be capable of detecting, constraining, or excluding, several existing models with 1 yr of observation.     

Photochemical studies on a phenolic phenylcoumarone lignin model molecule in relation to the photodegradation of lignocellulosic materials. Part 1. Structure of the photoproducts

The contribution of phenols, absorbing above 300 nm, to the photodegradation of lignin was approached by studying a phenolic phenylcoumarone lignin model molecule PCO. The compound was irradiated in solution and adsorbed on filter paper. The isolation and analysis of the photoproducts formed during the irradiation indicate the presence of a catechol structure (involving demethylation of the starting material) and two dimeric stilbene compounds: a ketone and a conjugated quinone methide giving high colouration to the irradiated solution. Those compounds have been detected as well in the solid state. The structure elucidation of the photoproducts was mainly based on mass spectrometry and 2D NMR experiments at 500 MHz. The major role played by the phenol group was supported by studying the O-methylated analogue PCOMe.     

Novel use of glow discharge optical emission spectroscopy (GDOES) to study corrosion of AA2024‐T3 in the presence and absence of inhibitors

Recent interest in environmentally friendly alternatives to chromate‐based corrosion inhibitors has led to the development of a range of novel coating formulations. The work described herein is aimed at developing a novel methodology to contribute to investigation of the self‐healing and active corrosion protection of the new coatings. An experimental procedure has been developed to model a defect in the coating by fixing coated specimens in close proximity to the uncoated AA2024‐T3, each separated by a narrow gap containing sodium chloride solution. After exposure to the corrosive environment, elemental depth profiles of the uncoated specimens were acquired by glow discharge optical emission spectroscopy (GDOES). The depth profiles of selected elements (notably aluminium, oxygen and copper) were shown to have characteristics which can be correlated with bulk surface roughening/intensity of corrosion, the thickness of the corroded layer and de‐alloying/re‐distribution of copper. An unanticipated inhibitory effect was noted in the case of a coating doped with γ‐Al₂O₃ (γ‐alumina or AluOx). Copyright © 2015 John Wiley & Sons, Ltd.     

Effect of Silk Protein Processing on Drug Delivery from Silk Films

Sericin removal from the core fibroin protein of silkworm silk is a critical first step in the use of silk for biomaterial‐related applications, but degumming can affect silk biomaterial properties, including molecular weight, viscosity, diffusivity and degradation behavior. Increasing the degumming time (10, 30, 60, and 90 min) decreases the average molecular weight of silk protein in solution, silk solution viscosity, and silk film glass‐transition temperature, and increases the rate of degradation of a silk film by protease. Model compounds spanning a range of physical‐chemical properties generally show an inverse relationship between degumming time and release rate through a varied degumming time silk coating. Degumming provides a useful control point to manipulate silk's material properties.

     

Laser flash photolysis of iodine-iodide mixture in hydroxylic solvent. Evidence for the existence of the radical anion I

The laser flash photolysis of iodine-iodide mixtures in alcoholic solvents produces transient species absorbing in the red and near infrared region with maxima at 740 and 590 nm. The 740 nm absorption band has already been attributed to the well known I

ion. In this work the 590 nm absorption band is assigned to the I

radical anion which presumably could be formed by the equilibrium reaction: I

+ I₃^- ? I

. The variations of the intensities of the 590 and 740 nm transient absorption bands as a function of I₃^? concentration, temperature and solvent, support this assignment. The kinetics of formation of I

and I

has been studied in solutions of tertiary butanol. An analysis of the experimental results shows that the I

ion could be formed via a mechanism involving an I

intermediate.     

The Robinson-Trautman type III prolongation structure containsK 2

The minimal prolongation structure for the Robinson-Trautman equations of Petrov type III is shown to always include the infinite-dimensional, contragredient algebra,K ₂, which is of infinite growth. Knowledge of faithful representations of this algebra would allow the determination of Bäcklund transformations to evolve new solutions.     

The mechanism of the norrish type II reaction of α-keto-acids and esters

Methyl-α-keto-octanoate undergoes a Type II reaction to give pent-1-ene and photophysical measurements show that this and the Type II reactions of α-keto-acids occur, contrary to previous claims, from the excited singlet state.