A simple strategy to generate light-responsive azobenzene-containing epoxy networks

Azobenzene containing epoxy networks are a class of photosensitive materials characterized by high thermal, optical and mechanical stability, promising for reversible optical storage applications. Here, we propose an encouraging two-step method to fabricate crosslinked coatings by simply reacting an amine-functionalized azobenzene and an epoxy resin in bulk for specified times to get soluble products (network precursors). Thin films based on these precursors were prepared, and thermally crosslinked in order to obtain high-T_g materials. The optical response of the materials was determined, both before and after crosslinking. In the case of the samples as prepared, the dynamic time response of the system is fast, as well as the relaxation of the photoinduced birefringence, as expected due to the high mobility of the chromophore. On the other hand, crosslinked systems have a slightly slower response, but higher values of remnant birefringence, providing stability of the photoinduced orientation, what makes them promising materials to use in optical storage applications. Besides, further analysis on the effect of temperature on the induced birefringence of the polymeric networks was also conducted to help optimization of material design. Finally, we had presented some preliminary investigations of surface relief grating recording in the obtained new materials.     

Polymeric coatings for photostability enhancement of poly(p‐phenylene vinylene) derivative films

Poly(p‐phenylene vinylene) (PPV) derivatives are an important class of conjugated polymers, known for their applications as electroluminescent materials for light‐emitting devices and sensors. These derivatives are highly susceptible to photodegradation by the combined action of oxygen and light. Here, the use of various commercial polymers as protective coatings against the photodegradation of PPV derivatives was explored. Cast films of two similar PPV derivatives, poly[(2‐methoxy‐5‐n‐hexyloxy)‐p‐phenylene vinylene] and poly[2‐methoxy‐5‐(2‐ethylhexyloxy)‐p‐phenylene vinylene], were submitted to photodegradation by exposure to white light under atmospheric conditions in order to verify if the type of side chain (linear or branched) had an effect on the photodegradation. No significant differences in the photodegradation behaviour between the two polymers were noticed. The following commercial polymers were tested as protective coatings for the PPV derivative cast films: 99 and 80% hydrolysed poly(vinyl alcohol) (PVA) and starch. The best results were achieved using coatings of 99% hydrolysed PVA, which increased about 700 times the time necessary for complete degradation of the PPV derivative films. The results show the effectiveness of this coating in minimizing and, possibly, controlling the effects of the photodegradation of PPV derivative films, which can be useful in many applications, e.g. oxygen sensors. Copyright © 2009 Society of Chemical Industry     

Control Flow Analysis for BioAmbients

This paper presents a static analysis for investigating properties of biological systems specified in BioAmbients. We exploit the control flow analysis to decode the bindings of variables induced by communications and to build a relation of the ambients that can interact with each other. We eventually apply our analysis to an example of gene regulation by positive feedback taken from the literature.     

Effect of chemical treatments on the mechanical and thermal behaviour of okra (Abelmoschus esculentus) fibres

The effect of a number of chemical treatments on the mechanical (tensile), thermal (FTIR, TGA) and water absorption properties of okra (Abelmoschus esculentus) fibres has been studied. These included: bare scouring of the fibres; bleaching (pure, and followed by acetylation or alkalisation); pure acetylation; sodium sulphite; sulphuric acid with potassium permanganate. Tensile properties of the fibres were studied using Weibull statistics and correcting the values obtained by the void content measured from SEM images. A separate set of SEM images allowed also characterising their failure mode. The general trend of the results shows some decrease in mechanical properties by all treatments, although the effect is partially concealed by the high variation of fibre dimensions and the relative variation of void content. Fracture surfaces present an increased level of twisting as an effect of chemical modification resulting in reduced adhesion force between the fibrils, though seldom in their physical separation. Treatments involving acetylation result in limited fibre degradation, whilst bleaching, scouring and particularly permanganate treatment, though mechanically damaging for the fibres, have lower influence on their thermal behaviour. Water absorption profile is significantly improved by all applied treatments.     

Thermal and viscoelastic behaviour of copolymers of propene and 1-hexene

Summary The thermal and viscoelastic behaviour of several copolymers of propene and 1-hexene have been studied in a wide range of compositions. The samples were prepared with a Ziegler-Natta catalyst with both internal and external donors. A significant amount of crystallinity has been found for the sample with a comonomer content as high as 19 mol %. The dynamic mechanical results show a considerable decrease of the storage modulus in the copolymers in relation to that of iPP. A single relaxation, corresponding to the glass transition, has been found in all the samples. Only the copolymer with the highest hexene content seems to display the beginning of another relaxation at low temperature.     

In vitro corrosion of some Co-Cr and Ni-Cr alloys used for removable partial dentures: influence of heat treatments

The influence of heat treatments on the corrosion resistance of some base-metal alloys currently used in dentistry as a base for porcelain substrate systems has been investigated. Four Co-Cr alloys (Wironit, Wironit extra hard, Wirobond and Wirolloy) and two Ni-Cr alloys (Wiron 88 and Wirolloy) were submitted to heat treatments for 30 min at 880, 980, 1080 °C for 30 min, and slowly cooled in air. The electrochemical characterization was performed by means of anodic polarization curves in Ringer's solution and artificial saliva at 37 °C. In both solutions it was found that ageing at 880 °C detrimentally affects the corrosion resistance of Co-Cr alloys; the passive zone is narrow and shows rather high current densities. On the contrary, the samples annealed at 1080 °C display a superior corrosion resistance. With Wiron 88 the effect is opposite, but the electrochemical behaviour of Wirolloy, is not affected by heat treatments; although it does have a more negative transpassive potential in artificial saliva and cannot be passivated in Ringer's solution. The SEM examination of the alloys evinces the microstructural modifications induced by heat treatments responsible for changes in the corrosion behaviour of the base-metal alloys.     

Protective action towards aluminium corrosion by silanes with a long aliphatic chain

A noticeable and persistent protective action towards aluminium corrosion can be obtained by treatments with silane molecules containing a long aliphatic chain (e.g., n-octadecyl-trimethoxy-silane, C18), which can markedly increase the barrier properties of the silanic coating. At variance with other silanic compounds, the layer of C18, although not uniform, tends to cover the whole aluminium surface completely and, in fact, its EIS spectra initially present one time constant only. It is likely that v.d.Waals interactions between the alkyl chains of C18 can lead to the formation of a polymolecular layer. The aqueous salt solutions may permeate through this layer, but with greater difficulties than in the case of an efficient di-silyl derivative (e.g., 1,2-bis-trioxymethyl-silyl-ethane, BTSE). C18 coatings noticeably retard not only the cathodic oxygen reduction reaction, but also the anodic metal oxidation process. A very prolonged action is also found towards the pitting process in the particularly aggressive chloride solution.     

RNA-mediated transformation in Aspergillus nidulans recovers gene functions lost by deletion or by point mutations

This work presents the results on two different approaches of RNA-mediated transformation in A. nidulans: a) the receptor strain was an argB2 (III) mutant deficient in arginine (OTCase deficient), and b) the receptor was an A. nidulans mutant defective in nitrate reductase synthesis due to a deletion in the niaD gene (VIII). The analyses of the arg+ and the nia+ retrotransformants allowed an insight on the fate and inheritance of the newly acquired characteristics. The occurrence and the study of Gene Inactivation Mechanism (RIP-like) inactivating the expression of extra copies of genes ectopically scattered over the receptor genome, was a byproduct of this research. Retrotransformants were also used as RNA-donor for a second turn of retrotransformation of the argB and niaD receptor strains. Genetic analyses of the new retrotransformants proved that the retrotransformation ability is kept by the re-extracted RNA when used in a second round of transformation process. This is the best genetic evidence that the newly acquired genetic characteristics were cDNA inserted, precisely transcribed and expressed. These are the first in vivo evidences of genetic information transference mediated by homologous RNA in lower eukaryotes.     

A Beckwith–Wiedemann-Associated CDKN1C Mutation Allows the Identification of a Novel Nuclear Localization Signal in Human p57Kip2

p57^Kip2 protein is a member of the CIP/Kip family, mainly localized in the nucleus where it exerts its Cyclin/CDKs inhibitory function. In addition, the protein plays key roles in embryogenesis, differentiation, and carcinogenesis depending on its cellular localization and interactors. Mutations of CDKN1C, the gene encoding human p57^Kip2, result in the development of different genetic diseases, including Beckwith–Wiedemann, IMAGe and Silver–Russell syndromes. We investigated a specific Beckwith–Wiedemann associated CDKN1C change (c.946 C>T) that results in the substitution of the C-terminal amino acid (arginine 316) with a tryptophan (R316W-p57^Kip2). We found a clear redistribution of R316W-p57^Kip2, in that while the wild-type p57^Kip2 mostly occurs in the nucleus, the mutant form is also distributed in the cytoplasm. Transfection of two expression constructs encoding the p57^Kip2 N- and C-terminal domain, respectively, allows the mapping of the nuclear localization signal(s) (NLSs) between residues 220–316. Moreover, by removing the basic RKRLR sequence at the protein C-terminus (from 312 to 316 residue), p57^Kip2 was confined in the cytosol, implying that this sequence is absolutely required for nuclear entry. In conclusion, we identified an unreported p57^Kip2 NLS and suggest that its absence or mutation might be of relevance in CDKN1C-associated human diseases determining significant changes of p57^Kip2 localization/regulatory roles.