Brittle to Quasi-Brittle Transition

Abstract. The present study focuses on the kinetic and non-deterministic aspects of the brittle to quasi-brittle transition. A solid is approximated by a lattice formed by the interacting continuum particles and the evolution of damage is estimated using particle dynamics. The onset of transition is measured by the rate of the change of correlation length. The proposed method is illustrated on the examples of creep rupture, strain localization and dynamic expansion of a circular void in a brittle plate.Sommario. Viene posta l'attenzione sugli aspetti cinetici e non deterministici della transizione dal comportamento fragile a quello quasi-fragile. Un solido viene approssimato da un reticolo formato da particelle interagenti e l'evoluzione del danno viene stimata tramite la dinamica delle particelle. L'inizio della transizione viene misurato tramite la variazione della lunghezza di correlazione. Il metodo proposto viene illustrato su esempi di rottura per creep, localizzazione della deformazione e l'espansione di un foro circolare in una piastra fragile.     

Diffusion-controlled melting and re-solidification of metal micro layers on a reactive substrate

The paper offers a theoretical approach to a prediction of residue formation inherent to melting and subsequent solidification of micro layers of molten aluminum alloys. The residue formation follows a reactive flow of a portion of the melt that is removed by a surface tension action. The residue portion solidifies in situ. The phenomenon studied is associated with materials’ processing during controlled atmosphere brazing of aluminum. The model assumes that diffusion of Silicon, present in an Al+Si clad of a brazing sheet, has a twofold role. First, a solid state Si diffusion prior to melting and across the clad–core interface of a composite brazing sheet takes place and modifies alloys’ composition on both sides of the interface. Subsequently, Si diffusion within clad controls the melting process. Both processes are essential for clad residue formation. The approach advocated in this paper leads to a prediction of the residue formation through a modeling of the non-equilibrium diffusion-controlled melting. A heuristic interpretation of physical mechanisms was discussed and a related mathematical model devised. The model was solved numerically in terms of Si concentration distributions for a moving boundary problem and corroborated with empirical data. Empirical data were gathered using an experimental controlled atmosphere brazing facility. The results of the modeling and their corroboration with the experimental data indicate a strong dependence of residue formations on the pre-melting state of the clad, in particular on the grain size within Al-clad matrix. A good agreement between numerically predicted residue mass and experimental findings is documented in detail.     

Lytic transglycosylase MltB of Escherichia coli and its role in recycling of peptidoglycan strands of bacterial cell wall

The cell wall is an indispensable structure for the survival of bacteria and a target for antibiotics. Peptidoglycan is the major constituent of the cell wall, which is comprised of backbone repeats of N-acetylglucosamine (NAG) and N-acetylmuramic acid (NAM). A peptide stem is appended to the NAM unit, which in turn experiences cross-linking with a peptide from another peptidoglycan in the final steps of cell wall assembly. In the normal course of bacterial growth, as much as 60% of the parental cell wall is recycled, a process that is not fully understood. A polymeric cell wall is fragmented by the family of lytic transglycosylases, and certain key fragments are transported to the cytoplasm for recycling. The genes for the six known lytic transglycosylases of Escherichia coli were cloned, and the enzymes were purified in this study. It is shown that MltB is the only lytic transglycosylase to turn over a synthetic peptidoglycan fragment of two NAG-NAM repeats; hence this enzyme is likely to be the lytic transglycosylase responsible for processing of shorter peptidoglycan strands. Lytic transglycosylases have been proposed to go through an oxocarbenium species that would trap the 6-hydroxyl moiety of the glucosamine residue of muramic acid to generate the so-called 1,6-anhydromuramyl moiety. It is documented herein by characterization of the products of turnover that this process takes place to the total exclusion of the entrapment of a water molecule by the reactive intermediary oxocarbenium species. Furthermore, turnover of the E. coli sacculus (whole cell wall) by MltB was characterized. It is documented that each MltB molecule is able to process the cell wall 14000 times in the course of a single doubling time for E. coli.     

Hurewicz sets of reals without perfect subsets

We show that even for subsets of the real line that do not contain perfect sets, the Hurewicz property does not imply the property , asserting that for each countable family of open -covers of , there is a choice function whose image is a -cover of . This settles a problem of Just, Miller, Scheepers, and Szeptycki. Our main result also answers a question of Bartoszyński and the second author, and implies that for , the conjunction of Sakai's strong countable fan tightness and the Reznichenko property does not imply Arhangelskiı's property .

     

Copolymerization of propylene oxide and CO2 using achiral salophen Co(III) penta-florobenzoate as catalyst and tetrabutyl ammonium bromide as co-catalyst

Copolymerization of racemic propylene oxide with carbon dioxide is investigated in the presence of economically inexpensive and effective achiral salophenCo(III)X [salophen = N,N'-bis(3,5-di-tert-butylsalicylidene)-phenylenediimine, X = pentaflorobenzoate] catalyst and tetrabutyl ammonium bromide as co-catalyst. Effects of different variables like monomer to catalyst ratio, catalyst/co-catalyst ratio, temperature, pressure of CO₂ on molecular weight, yield and selectivity of poly(propylene carbonate) [PPC] have been investigated. The maximum M_w of 25.8 g/mol has been obtained at 15 bar and 50°C. All the samples were found to have excellent polydispersity near to 1.     

Comparative TOF-SIMS and MALDI TOF-MS analysis on different chromatographic planar substrates

A comparison is made between two high resolution, surface-based, mass spectrometric methods: time-of-flight secondary ion mass spectrometry (TOF-SIMS) and matrix-assisted laser desorption/ionisation mass spectrometry (MALDI TOF-MS) in indication of abietic and gibberellic acids molecular profiles on different chromatographic thin layers. The analytes were applied to silica gel chromatographic thin layers with SIMS on-line interfacing channel, monolithic silica gel ultra-thin layers, and thin layers specifically designed for direct Raman spectroscopic analysis. Two MALDI matrices were used in this research: ferulic acid and 2,5-dihydroxybenzoic acid. The silica gel SIMS-interfacing channel strongly supported formation of numerous different MALDI MS fragments with abietic and gibberellic acids, and ferulic acid matrix. The most intense fragments belonged to [M-OH](+) and [M](+) ions from ferulic acid. Intense conjugates were detected with gibberellic acid. The MALDI MS spectrum from the monolithic silica gel surface showed very low analyte signal intensity and it was not possible to obtain MALDI spectra from a Raman spectroscopy treated chromatographic layer. The MALDI TOF MS gibberellic acid fragmentation profile was shielded by the matrix used and was accompanied by poor analyte identification. The most useful TOF-SIMS analytical signal response was obtained from analytes separated on monolithic silica gel and a SIMS-interfacing modified silica gel surface. New horizons with nanostructured surfaces call for high resolution MS methods (which cannot readily be miniaturised like many optical and electrochemical methods) to be integrated in chip and nanoscale detection systems.     

Raman spectroscopy probing of self-assembled monolayers inside the pores of gold nanotube membranes

Electroless deposition was used to coat porous alumina membranes with gold. This process reduced the pore diameters and provided a platform suitable for surface modifications with self assembled monolayers (SAMs). The surface enhanced Raman scattering (SERS) effect was employed in order to confirm and characterise the formation of SAMs of 3-mercaptobenzoic acid (mMBA) inside the pores of gold nanotube membranes prepared using porous alumina (PA) templates. The investigation of the coverage and reproducibility of SAMs within porous matrices is of utmost importance in the design of filtration membranes and sensing platforms. Raman spectroscopy is capable of spatially resolved techniques such as mapping which was used to characterise the distribution of mMBA assembly within the pores. Due to the highly ordered structure of porous alumina and well controlled electroless gold deposition, these gold coated membranes have the potential to develop into SERS active substrates for ultrasensitive sensing technologies.     

Computational probe of cavitation events in protein systems

Previous all-atom simulations have identified several classes of proteins where hydrophobic de-wetting (cavitation) is at play. Here we develop and validate a computationally fast method that predicts in which protein systems water spontaneously cavitates. We implement a cubic lattice model, which incorporates the protein shape from crystallographic data and the protein-water interactions from thermodynamic data. Combining it with the previously developed coarse-grained model for water, we determine the extent of occupancy of water at protein-protein interfaces and in protein-ligand cavities. The model captures essential findings from all-atom molecular dynamics studies on the same systems by distinguishing protein cavities that dry from those that remain wet. We also interpret the origin of the cavitation inside the melittin tetramer on simple thermodynamic grounds, and show that part of the mellitin surface is sufficiently hydrophobic to trigger cavitation. Using Glauber/Kawasaki dynamics we obtain the time-scales for de-wetting events that are in agreement with those from all-atom simulations. The method can serve as an intermediate step between the necessary initial screening that identifies proteins with abundance of hydrophobic patches using bioinformatics tools (L. Hua, X. H. Huang, P. Liu, R. H. Zhou and B. J. Berne, J. Phys. Chem. B, 2007, 111, 9069), and computationally extensive studies that need to incorporate molecular details (e.g. single mutation studies of amino acid residues).     

Fluorescence Dynamics of Coumarin C522 as a Function of Micelle Confinement along with Cyclodextrin Supramolecular Complex Formation

Our aim is to doubly confine a molecule of coumarin C522 in a host–guest supramolecular complex with β‐cyclodextrin in a reverse sodium dioctyl sulfosuccinate (AOT) micelle using nonpolar n‐heptane and polar water solvents. Varying the volumes of coumarin C522 and β‐cyclodextrin dissolved in water allows us to control the water‐pool diameters of the reverse micelle in n‐heptane with values of w=3, 5, 10, 20, and 40, where w is the ratio of water concentration to AOT concentration in n‐heptane. To study the fluorescence dynamics of coumarin C522, the spectral steady‐state and time‐resolved dependences are compared for the two systems coumarin C522(water)/AOT(n‐heptane), denoted C522/micelle, and coumarin C522/β‐cyclodextrin(water)/AOT(n‐heptane), referred to as C522/CD/micelle. The formation of the supramolecular host–guest complex CD–C522 is indicated by a blue shift, but in the micelle, the shift is red. However, the values of the fluorescence maxima at 520 and 515 nm are still way below the value of 535 nm representing bulk water. The interpretation of the red shift is based on two complementary processes. The first one is the confinement of CD and C522 by the micelle water pool and the second is the perturbation of the micelle by CD and C522, resulting in an increase of the water polarity. The fluorescence spectra of the C522/micelle and C522/CD/micelle systems have maxima and shoulders. The shoulder intensities at 440 nm, representing the C522 at n‐heptane/AOT interface, decrease as the w values decrease. This intensity shift suggests that the small micelle provides a stronger confinement, and the presence of CD shifts the equilibrium from n‐heptane towards the water pool even more. The fluorescence emission maxima of the C522/micelle and C522/CD/micelle systems for all w values clearly differentiate two trends for w=3–5, and w=10–40, suggesting different interaction in the small and large micelles. Moreover, these fluorescence maxima result in 7 and 13 nm differences for w=3 and w=5, respectively, and provide the spectral evidence to differentiate the C522 confinement in the C522/micelle and C522/CD/micelle systems as an effect of the CD molecule, which might be interpreted as a double confinement of C522 in CD within the micelle. The ultrafast decay in the case of w=3 ranges from 9.5 to 16 ps, with an average of 12.6 ps, in the case of the C522/micelle system. For C522/CD/micelle, the ultrafast decay at w=3 ranges from 9 to 14.5 ps, with an average of 11.8 ps. Increasing w values (from 10 to 40) result in a decrease of the ultrafast decay values in both cases to an average value of about 6.5 ps. The ultrafast decays of 12.6 and 11.8 ps for C522/micelle and C522/CD/micelle, respectively, are in the agreement with the observed red shift, supporting a double confinement in the C522/CD/micelle(w=3) system. The dynamics in the small and large micelles clearly show two different trends. Two slopes in the data are observed for w values of 3–5 and 10–40 in the steady‐state and time‐resolved data. The average ultrafast lifetimes are determined to be 12.6 and 6.5 ps for the small (w=3) and the large (w=40) micelles, respectively. To interpret the experimental solvation dynamics, a simplified model is proposed, and although the model involves a number of parameters, it satisfactory fits the dynamics and provides the gradient of permittivity in the ideal micelle for free water located in the centre (60–80) and for bound water (25–60). An attempt to map the fluorescence dynamics of the doubly confined C522/CD/micelle system is presented for the first time.     

Polymeric Microfiltration Membranes Modification by Supercritical Solvent Impregnation—Potential Application in Open Surgical Wound Ventilation

This study investigated supercritical solvent impregnation of polyamide microfiltration membranes with carvacrol and the potential application of the modified membranes in ventilation of open surgical wounds. The impregnation process was conducted in batch mode at a temperature of 40 °C under pressures of 10, 15, and 20 MPa for contact times from 1 to 6 h. FTIR was applied to confirm the presence of carvacrol on the membrane surface. In the next step, the impact of the modification on the membrane structure was studied using scanning electron and ion beam microscopy and cross-filtration tests. Further, the release of carvacrol in carbon dioxide was determined, and finally, an open thoracic cavity model was applied to evaluate the efficiency of carvacrol-loaded membranes in contamination prevention. Carvacrol loadings of up to 43 wt.% were obtained under the selected operating conditions. The swelling effect was detectable. However, its impact on membrane functionality was minor. An average of 18.3 µg of carvacrol was released from membranes per liter of carbon dioxide for the flow of interest. Membranes with 30–34 wt.% carvacrol were efficient in the open thoracic cavity model applied, reducing the contamination levels by 27% compared to insufflation with standard membranes.