Volatile Organic Compounds of Conspecific-Damaged Eucalyptus benthamii Influence Responses of Mated Females of Thaumastocoris peregrinus

Plants respond to herbivory by synthesizing and releasing novel blends of volatile organic compounds (VOCs). Natural enemies are attracted to these VOCs, but little is known about the effects of these chemicals on the herbivores themselves. We studied the effect of Thaumastocoris peregrinus herbivory on VOCs released by Eucalyptus benthamii plants and the responses of this herbivore to the VOCs. In total, 12 compounds released by E. benthamii were identified. Five compounds (β-pinene, linalool, 9-epi-(E)-caryophyllene, viridiflorol, and one unidentified compound) emitted after herbivore and mechanical damage were not detected in collections from undamaged plants. The three most abundant VOCs, α-pinene, aromadendrene, and globulol, were released in greater quantities from herbivore-damaged plants compared to plants with mechanical damage, which, in turn, released greater amounts than undamaged (control) plants. The VOCs emitted after herbivore damage did not differ during the photophase and scotophase in either quantity or quality. In an olfactometer, mated female T. peregrinus showed a preference for undamaged plants over herbivore-damaged plants, and also for hexane over α-pinene at an amount equivalent to that released by a herbivore-damaged plant. In the olfactometer, virgin females did not exhibit any preference between conspecific-damaged or undamaged plants.     

Formalising the Fisherman's Folly puzzle

This paper investigates the challenging problem of encoding the common sense knowledge involved in the manipulation of spatial objects from a reasoning about actions and change perspective. In particular, we propose a formal solution to a puzzle composed of non-trivial objects (such as holes and strings) assuming a version of the Situation Calculus written over first-order Equilibrium Logic, whose models generalise the stable model semantics.     

Development of films based on blends of gelatin and poly(vinyl alcohol) cross linked with glutaraldehyde

Both gelatin and poly(vinyl alcohol) (PVA) can be cross linked with glutaraldehyde (GLU). In the case of gelatin, the GLU reacts with each ε-NH2 functional group of adjacent lysine residues, while for PVA, the GLU reacts with two adjacent hydroxyl groups, forming acetal bridges. Thus it can be considered possible to cross link adjacent macromolecules of gelatin and PVA using GLU. In this context, the aims of this work were the development of biodegradable films based on blends of gelatin and poly(vinyl alcohol) cross linked with GLU, and the characterization of some of their main physical and functional properties. All the films were produced from film-forming solutions (FFS) containing 2 g macromolecules (PVA + gelatin)/100 g FFS, 25 g glycerol/100 g macromolecules, and 4 g GLU (25% solution)/100 g FFS. The FFS were prepared with two concentrations of PVA (20 or 50 g PVA/100 g macromolecules) and two reaction temperatures: 90 or 55 °C, applied for 30 min. The films were obtained after drying (30 °C/24 h) and conditioning at 25 °C and 58% of relative humidity for 7 days, and were then characterized. The results for the color parameters, mechanical properties, phase transitions and infrared spectra showed that some chemical modifications occurred, principally for the gelatin. However, in general, all the characteristics of the films were either typical of films based on blends of these macromolecules without cross linking, or slightly higher. A greater improvement in the properties of this material was probably not observed due to the crystallinity of the PVA, which has a melting point above 90 °C. The presence of microcrystals in the polymer chain probably reduced macromolecular mobility, hindering the reaction. Thus more research is necessary to produce biodegradable films with improved properties.     

Bulk modulus of basic sodalite, Na8[AlSiO4]6(OH)2·2H2O, a possible zeolitic precursor in coal-fly-ash-based geopolymers

Synthetic basic sodalite, Na₈[AlSiO₄]₆(OH)₂·2H₂O, cubic, P43n, (also known as hydroxysodalite hydrate) was prepared by the alkaline activation of amorphous aluminosilicate glass, obtained from the phase separation of Class F fly ash. The sample was subjected to a process similar to geopolymerization, using high concentrations of a NaOH solution at 90 °C for 24 hours. Basic sodalite was chosen as a representative analogue of the zeolite precursor existing in Na-based Class F fly ash geopolymers. To determine its bulk modulus, high-pressure synchrotron X-ray powder diffraction was applied using a diamond anvil cell (DAC) up to a pressure of 4.5 GPa. A curve-fit with a truncated third-order Birch–Murnaghan equation of state with a fixed K'_o = 4 to pressure-normalized volume data yielded the isothermal bulk modulus, K_o = 43 ± 4 GPa, indicating that basic sodalite is more compressible than sodalite, possibly due to a difference in interactions between the framework host and the guest molecules.     

13C NMR study of presence of uron structures in amino adhesives and relation with wood‐based panels performance

The chemical structure of amino adhesives produced by the strongly acid process was investigated by ¹³C Nuclear Magnetic Resonance spectroscopy. This technique allowed the identification of functional groups and its quantitative determination. Concentration of cyclic polymeric structures (urons) was shown to be related with adhesive performance and with particleboard physico‐mechanical properties and formaldehyde content. Higher urons concentration presented lower viscosity and reactivity. Particleboards produced with resins with lower urons concentration presented lower formaldehyde content, but also lower internal bond strength. Wood‐based panels produced fulfilled E1 class requirements for formaldehyde emissions, indicating that strongly acid process is an alternative to the conventional alkaline–acid process. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 4500–4507, 2013     

The effect of methanol on the stability of Pt/C and Pt–RuOx/C catalysts

The behavior of Pt/C and Pt–RuO_x/C electrodes subjected to a larger number of potential scans and constant potential for prolonged time periods was investigated in the absence and presence of methanol. The structural changes were analyzed on the basis of the modifications observed in the X-ray diffraction pattern of the catalysts. Carbon monoxide stripping experiments were performed before and after the potential scans, thus enabling analysis of the behavior of the electrochemically active surface area. The resulting solutions were examined by inductively coupled plasma mass spectrometry (ICP-MS). There was reduction in the electrochemically active surface area, as well as increase in crystallite size and dissolution of catalyst components after the potential scan tests. Catalyst degradation was more pronounced in the presence of methanol, and cyclic potential conditions accelerate the degradation mechanisms.     

(Virtual) Agents for running electricity markets

This paper describes a multi-agent based simulation (MABS) framework to construct an artificial electric power market populated with learning agents. The artificial market, named TEMMAS (The Electricity Market Multi-Agent Simulator), explores the integration of two design constructs: (i) the specification of the environmental physical market properties and (ii) the specification of the decision-making (deliberative) and reactive agents. TEMMAS is materialized in an experimental setup involving distinct power generator companies that operate in the market and search for the trading strategies that best exploit their generating units’ resources. The experimental results show a coherent market behavior that emerges from the overall simulated environment.     

Using finite element modeling to examine the flow processes in quasi-constrained high-pressure torsion

Finite element modeling was used to examine the flow processes in high-pressure torsion (HPT) when using quasi-constrained conditions where disks are contained within depressions on the inner surfaces of the upper and lower anvils. Separate simulations were performed using applied pressures from 0.5 to 2.0 GPa, rotations up to 1.5 turns and friction coefficients from 0 to 1.0 outside of the depressions. The simulations demonstrate the distribution of effective strain within the depressions is comparable to the prediction by ideal torsion, and the applied pressure and the friction coefficient outside the depressions play only a minor role in the distribution of effective strain. The mean stresses during processing vary linearly with the distance from the center of the disk such that there are higher compressive stresses in the disk centers and lower stresses at the edges. The torque required for rotation of the anvil is strongly dependent upon the friction coefficient between the sample and the anvil outside the depressions.     

Characterisation of enzymatically oxidised lignosulfonates and their application on lignocellulosic fabrics

BACKGROUND: The ‘double function’ of laccase, from the ascomycete Myceliophthora, to depolymerise/polymerise lignin was studied in this work. A lignosulfonate (LS) compound was oxidised by enzymatic action and several techniques were applied to measure the polymeric changes obtained. This study was focused on the attachment level of the oxidised LS at the flax surface. RESULTS: Modified solutions were studied in terms of surface charge. Zeta potential values obtained showed an increase of polymerisation after several days of incubation. The change in molecular weight after LS polymerisation was detected using gel permeation chromatography. An increase of 1700 Da was achieved. Fourier transform infrared and UV‐visible spectroscopy techniques were applied and the results showed an increase of the degree of polymerisation. The colour strength of flax fabrics incubated with oxidised LS solutions was also measured and an increase of K/S (K, absorption coefficient; S, scattering coefficient) after enzymatic oxidation was observed. CONCLUSION: The oxidised lignin products obtained show good potential for use in natural surface modification of textile materials containing flavonoids. These findings have important practical implications for lignocellulosic fibre coloration, where new polymers can replace harsh chemicals in the textile industry. Copyright © 2009 Society of Chemical Industry