Sustainable resilience of hydrogen energy system

Resilience is the capacity of complex system to be recovered after a sudden change of the indicator. Energy resilience is the ability of energy system to provide and maintain an acceptable level of service in the face of various challenges to normal operation. Loss of resilience can cause loss of valuable energy system services, and may even lead to rapid transitions or shifts into qualitatively different situations and configurations,     

Synthesis and characterization of water-based poly(vinyl acetate-co-butyl acrylate) latexes containing oligomeric protective colloid

Poly(vinyl acetate-co-butyl acrylate) latexes having oligomeric N-methylol acrylamide were prepared by semi-continuous emulsion polymerization. The effects of new protective colloid and comonomer ratios on the physicochemical and colloidal properties of latexes were investigated. The changes in homopolymer and copolymer latexes were determined by measuring viscosity, particle size, molecular weight (MW), molecular weight distribution (MWD), and surface tension. [`(M)]<sub>n</sub> \bar{M}_{n} values of copolymer latexes were found to be lower than the MWs of the poly(vinyl acetate) and poly(butyl acrylate) homopolymers. In general, [`(M)]_n \bar{M}_{n} and [`(M)]_\textw \bar{M}_{\text{w}} values of copolymer latexes changed irregularly with increasing BuA ratio in the copolymer composition.     

A comparative study on water-based coatings prepared in the presence of oligomeric and conventional protective colloids

Poly(vinyl acetate-co-butyl acrylate) latexes were prepared by using semi-continuous emulsion polymerization method in presence of two different protective colloids which were oligomeric N-methylol acrylamide and conventional poly(vinyl alcohol). The effects of these protective colloids on colloidal, surface and film properties of latexes were examined. Poly(vinyl acetate-co-butyl acrylate) synthesized with oligomeric N-methylol acrylamide, which was characterized by FT-IR, NMR and MALDI-TOF MS, was found to have lower viscosity, finer particle size, better latex stability, lower polydispersity, higher T_g and better film forming behavior compared to those synthesized from the poly(vinyl alcohol).     

Some properties of thin medium density fiberboard panels treated with sunflower waste oil vapor

The objective of this study was to investigate the effect of hot waste oil vapor on some of the physical and bending properties of commercially manufactured thin medium density fiberboard (tMDF) panels. The samples were treated with waste oil vapor at a temperature of 220 °C for 10 and 20 min time durations. Based on the findings in this work, the water absorption and thickness swelling of the samples were improved by the treated panels with hot vapor oil and heat. It appears that the samples had some discoloration as a result of treatment processes. It was also observed that modulus of rupture (MOR) and modulus of elasticity (MOE) of the samples were adversely influenced. However, it seems that the thermal conductivity of the samples enhanced by such treatments. Panel products treated with these processes could have some promising potential in various applications including outdoor use.     

Swelling behavior of polystyrene networks in some aliphatic esters and linear polystyrene solutions

Summary Polystyrene networks were synthesized by free radical polymerization of styrene in the presence of dibenzoyl peroxide as an initiator, divinylbenzene as a crosslinker at 50 °C in toluene under nitrogen atmosphere. The swelling behavior of the synthesized polystyrene networks were studied at different temperatures in methyl acetate, ethyl acetate, propyl acetate, isopropyl acetate, butyl acetate, isobutyl acetate, tert-butyl acetate, and isopentyl acetate. Equations were given for the variation of the polymer-solvent interaction parameter, χ₁₂, as a function of reciprocal absolute temperature in the temperature range from 25 to 75 °C. Polystyrene networks were swollen in linear polystyrene solutions in toluene of different concentrations. Linear polystyrene samples were almost monodisperse and of high molecular weight. The equilibrium swelling degrees were evaluated using the Flory-Rehner theory. The relation of volume swelling ratio, q_v, to the volume fraction of the linear polymer in solution, φ, was evaluated and characterized by interaction parameter of crosslinked polystyrene with linear polystyrene, χ₂₃. The parameter χ₂₃ was found around zero as expected from mixtures of similar chemical structures by extrapolating the values of χ₂₃ at tested concentrations to zero solvent concentration.     

The ratio of crystallinity and thermodynamical interactions of polycaprolactone with some aliphatic esters and aromatic solvents by inverse gas chromatography

Summary The retention diagrams of benzene, toluene, ethyl benzene, chloro benzene, n-propyl benzene, isopropyl benzene, methyl acetate, ethyl acetate, n-propyl acetate, n-butyl acetate and isoamyl acetate on the polycaprolactone were plotted at temperatures between 70 and 140^oC by inverse gas chromatography technique. Percent crystallinity of polycaprolactone were obtained at temperatures below melting point from the retention diagrams of benzene, toluene and ethyl benzene. It was concluded that the data obtained by inverse gas chromatography were comparable those of obtained by differential scanning calorimetry. Specific retention volume, V_g^o, Flory-Huggins polymer-solvent interaction parameters, ₁₂, the weight fraction activity coefficients of the solvents at infinite dilution, ₁, effective exchange energy parameters, X_eff were determined. Later, the partial molar heat of sorption, H_1,sorp and the partial molar heat of mixing, H₁ were obtained from the slope of the logarithm of specific retention volume, Ln V_g^o versus 1/T plot and from the slope of the logarithm of the weight fraction activity coefficients, ₁versus 1/T plot, respectively.     

Synthesis and Photopolymerizations of New Crosslinkers for Dental Applications

Summary: Five new crosslinkers for use in dental composites were synthesized. Four are based on TBHMA: 1 via reaction of TBBr and Bisphenol A; 2 by hydrolysis of t‐butyl groups of the first monomer to give a diacid derivative; 3 by conversion of the first monomer to an amide derivative using benzyl amine; 4 by conversion of the first monomer to amide derivative using APTES. The AHM‐based monomer 5 was synthesized from the Michael addition of APTES to AHM. The photopolymerization behaviors of the synthesized monomers with Bis‐GMA, TEGDMA and HEMA were investigated using photodifferential scanning calorimetry at 40 °C using DMPA as photoinitiator. The polymerization rates and degrees of conversion for mixtures of any of the monomers 1 – 4 with Bis‐GMA:TEGDMA were found to be similar to Bis‐GMA:TEGDMA, higher than Bis‐GMA:HEMA, and also higher than mixtures with Bis‐GMA:HEMA. The incorporation of TBHMA‐based monomers into the conventional resin mixture (Bis‐GMA and TEGDMA) reduced the polymerization shrinkages. Monomer 5 and its mixtures polymerized much faster and to higher degrees of conversion than the other investigated systems, however, this system exhibited the largest volume shrinkage.

Structures of some of the new crosslinkers synthesized.     

Evaluating the in vitro bioaccessibility of phenolics and antioxidant activity during consumption of dried fruits with nuts

Dried fruits and nuts are considered as healthy snacks and they are often consumed together in the Turkish diet. In order to investigate the effect of codigestion of dried fruits (figs, apricots, raisins) together with nuts (almonds, walnuts, hazelnuts), total phenolics (TP) and total antioxidant capacity (TAC) have been evaluated spectrophotometrically at different phases of simulated gastrointestinal (GI) digestion, using an in vitro model. TP, ABTS and CUPRAC results revealed that for all fruit–nut mixtures, the amount recovered in the dialyzed fraction was lower than the recovery of fruits or nuts alone, indicating an antagonistic effect. On the other hand, DPPH results showed that for fig–walnut, fig–hazelnut and apricot–hazelnut mixtures the quantity recovered in the dialyzed fractions were 35–107% higher than the recovery of fruits or nuts alone, representing a synergistic effect. Similarly, FRAP results also demonstrated a synergistic effect in case of fig–walnut, apricot–walnut and apricot–hazelnut mixtures (10–74% higher recovery). Current study provides valuable insights into the changes taking place during in vitro GI digestion of dried fruits and nuts.     

Use of ionic liquid in leaching process of brass wastes for copper and zinc recovery

Brass ash from the industrial brass manufacturer in Turkey was leached using the solutions of ionic liquid （IL） 1-butyl-3-methyl-imi-dazolium hydrogen sulfate （[bmim]HSO4） at ambient pressure in the presence of hydrogen peroxide （H2O2） and potassium peroxymonosulfate （oxone） as the oxidants. Parameters affecting leaching efficiency, such as dissolution time, IL concentration, and oxidizing agent addition, were investigated. The results show that [bmim]HSO4 is an efficient IL for the brass ash leaching, providing the dissolution efficiencies of 99%for Zn and 24.82%for Cu at a concentration of 50vol%[bmim]HSO4 in the aqueous solution without any oxidant. However, more than 99%of zinc and 82%of copper are leached by the addition of 50vol%H2O2 to the [bmim]HSO4 solution. Nevertheless, the oxone does not show the promising oxidant behavior in leaching using [bmim]HSO4.     

Countries to benefit most from early transition to hydrogen fueled transportation: Merit factor analysis

The world consists of many countries having differences in many areas, ranging from size to economic level, from population to education, etc. Consequently, they are not going to convert to hydrogen‐fueled transportation at the same time. Some will have the right conditions to convert to clean hydrogen transportation early, and other countries will have conditions which will result in a delay in conversion to hydrogen‐fueled transportation. In order to find out which countries are the candidates for early conversion to hydrogen fueled transportation and which countries might convert to hydrogen‐fueled transportation later, an analysis has been carried out covering almost all of the countries in the world. Results indicate that the countries with higher income per capita and smaller size could convert to hydrogen‐fueled transportation earlier. Copyright © 2013 John Wiley & Sons, Ltd.