The effect of different porous media on moisture loss and oil absorption profiles during frying using glass micromodels

Microstructure plays a key role in oil absorption during frying. The aim of this work was to improve our understanding of the relationship between microstructure and oil absorption, through the use of glass micromodels to obtain evidence of transport phenomena in three porous networks. Micromodels were saturated with water and partially immersed in oil at 190°C. Moisture and oil profiles were imaged to get water and oil saturation maps. Image and fractal analyses were performed to describe the morphology of the evaporation and oil fronts. Results showed that higher porosity facilitated the moisture removal and promoted greater oil absorption during cooling. The fractal dimension showed that microstructures with a relatively high number of fine capillaries were less stable and propitiated fingering during the advance of the evaporation front. In all matrices, the disruption of the surface oil film due to air penetration was a critical factor to stop oil imbibition. © 2015 American Institute of Chemical Engineers AIChE J, 62: 629–638, 2016     

Organochlorine Formation in Tertiary Amine Catalyzed Pulp Bleaching

An oxygen delignified eucalyptus kraft pulp was bleached by applying a catalytic amount of a tertiary amine, 1,4-diazabicyclo[2,2,2]octane, and hypochlorous acid at varying pH, temperature, and time. The bleaching filtrate was analyzed for chloroform and AOX and the pulp for residual lignin, hexenuronic acid, and OX. In comparison with chlorine dioxide bleaching, the novel catalytic bleaching (pH < 6) generated only traces of chloroform and low contents of AOX and OX. Separate catalytic oxidations of authentic hexenuronic acid showed that it was a major precursor of chloroform. The results demonstrate a practical way to reduce organochlorine formation in pulp bleaching and provide new understanding on the reaction pathways that yield chloroform.     

Composites made from a soybean oil biopolyurethane and cellulose nanocrystals

Cellulose nanocrystals (CNC) obtained by acidic hydrolysis from microcrystalline cellulose were dispersed in a biopolyurethane matrix to prepare composite films. The polyurethane was prepared from a hydroxylated soybean oil (SO‐OH) and a polymeric diphenyldiisocyanate (pMDI), using a organotin compound as the catalyst. The composite films contained different concentrations of nanocelullose, without any macroscopic aggregates in all cases. Thermal, tensile and dynamic mechanical properties of the films were determined for all the samples. In particular, it was observed that the glass transition temperature of the nanocomposites slightly increased with the concentration of the cellulose nanocrystals. The nanocomposite with 1 wt% of nanocellulose showed the highest tensile strength of the series. POLYM. ENG. SCI., 58:125–132, 2018. © 2017 Society of Plastics Engineers     

Optimization of properties in a rubber compound containing a ternary polymer blend using response surface methodology

In order to find the best combination of three synthetic rubbers, that is, styrene‐butadiene rubber (SBR) grade 1712, SBR grade 1721 and high‐1,4‐cis polybutadiene, that produce a compound with specific end‐use properties, a statistical experimental design is proposed in this work. The design consists of ten mixtures containing specific amounts of total styrene and BR content. A number of properties are tested in each mixture, selecting those related to requirements for the tread of a high performance tire: glass transition temperature (T_g), the ratio between the viscous modulus and the elastic modulus (tanδ@60 °C), Mooney viscosity, and the tensile properties. The values obtained for each property are fit to statistically significant models, obtaining the respective response surfaces. These are next used to define a desirable formulation with the optimal ratio of each rubber, and finally the optimized formulation is validated by comparing the experimental and predicted values for each modeled property. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46548.     

Removal of sulfamethoxazole from waters and wastewaters by conductive‐diamond electrochemical oxidation

BACKGROUND: Sulfamethoxazole (SMX, used as a model bacteriostatic antibiotic) is persistent to conventional biological treatments of wastewaters. In this work, conductive‐diamond electrochemical oxidation (CDEO) was found to be an effective technology for its removal from the effluents of conventional wastewater treatment plants. RESULTS: The use of CDEO has been evaluated for the removal of the antibiotic SMX from water and wastewaters. The results show that CDEO can reduce the concentration of this organic pollutant to values below 0.1 µg dm^?3. The variation of the SMX concentration during electrolysis shows a complex shape with a plateau zone that increases in size with the initial concentration of SMX. This complex trend is not observed in the changes of TOC, which seems to indicate that the CDEO of SMX solutions does not lead directly to the generation of carbon dioxide as a final product. A tentative reaction pathway has been proposed based on a thorough analysis of the reaction mixture, in which the main intermediate products were identified. The use of liquid chromatography time‐of‐flight mass spectrometry (LC‐TOFMS) allowed the identification of nine organic intermediates (with M_w 98, 108, 172, 173, 197, 203, 227, 269 and 287) during the electrolysis and the concentration of these compounds depends on the initial SMX concentration and on the current density applied. CONCLUSIONS: CDEO is able to reduce the concentration of the organic pollutant below 0.1 mg dm^?3. SMX removal is faster than that of TOC. This fact indicates the formation of reaction intermediates. Analytical techniques show that nine reaction intermediates are generated in the system, and that their concentration depends on the initial SMX concentration and on the current density used. Copyright © 2012 Society of Chemical Industry     

The Composition of Mixed Micelles Formed by Dodecyl Trimethyl Ammonium Bromide and Benzethonium Chloride in Water

The composition of the mixed micelles formed by benzethonium chloride and dodecyl trimethyl ammonium bromide in water were experimentally determined by a combination of surfactant ion-selective electrodes and UV–Vis spectroscopy measurements. Results were compared with the computed compositions from three theories on mixed micelles available in the literature (Regular Solution, Motomura’ and Georgiev’s). The basis of the Junquera and Aicart method and the determination of the micelle aggregation number (N) by pyrene fluorescence quenching, i.e., the constancy of N and the mixed micelle composition when the total concentration is changed, were not supported by our experimental results. Experimental micelle compositions were statistically equal to those computed by Regular Solution Theory. The mixed micelle composition and the quantity of non-micellized surfactant molecules change with concentration above the critical micelle concentration, and therefore do not support the assumptions used in the Junquera and Aicart procedure and in the determination of N by pyrene fluorescence quenching. The reason why the latter procedure gives N values similar to those obtained from other techniques is discussed.     

Catalysts to improve the abatement of sulfamethoxazole and the resulting organic carbon in water during ozonation

Sulfamethoxazole (SMX), one pharmaceutical compound, has been treated in aqueous solutions with catalysts (copper and cobalt type perovskites and cobalt–alumina) and promoters (activated carbons). Hydrogen peroxide and saturated carboxylic acids were identified as intermediates. The effects of adsorption and pH have been investigated. Removal of the starting SMX accomplished with ozone alone is a fast process but catalytic or promoted ozonation is needed to significantly reduce the resulting organic carbon. SMX is, thus, mainly removed through direct ozone reaction while hydroxyl radical oxidation is the mechanism of removal the remaining TOC. The kinetics of the process has also been investigated. Perovskite catalytic ozonation resulted to be a chemical control process and apparent rate constants for homogeneous and heterogeneous ozonation were determined. For activated carbon ozonation, external diffusion of ozone to solid particles controlled the process rate.     

Fractal Extra-Framework Species in De-aluminated LaY Zeolites and Their Catalytic Activity

Lanthanum-containing Y (LaY) zeolites were prepared by ionic exchange from NaY parent zeolite. The LaY zeolites were de-aluminated by steaming. De-aluminated zeolites presented different Si/Al ratio. The physicochemical properties of these catalysts were characterized by X-ray diffraction, pyridine and xenon adsorption, infrared spectroscopy and ²⁹Si, ²⁷Al, ¹²⁹Xe, ¹³⁹La solid-state nuclear magnetic resonance spectroscopy. Furthermore, a fractal geometry approach was adopted to describe the evolution in the texture as a consequence of de-alumination. The catalytic properties of materials were evaluated in the n-hexane cracking reaction. The catalyst with the highest catalytic activity was the zeolite highest de-aluminated (Si/Al ratio of 3.7). Such performance was attributed on the one hand, to active extra-framework aluminum species hosted in the large cavities of zeolites and, on the other hand to redistribution of lanthanum species into the zeolite as a consequence of de-alumination.