Catalytic Vicinal Diacylation of Epoxidized Triglycerides in Canola Oil

The epoxy ring opening and vicinal diacylation of fatty acids in vegetable oils was found to be promising reaction to synthesize stable biolubricants and bioplasticizers. The current research investigation is emphasized on the synthesis of a value added product vicinally diacylated canola oil by sulfated‐ZrO₂. The two‐step research approach employed includes: (i) epoxidation, and (ii) epoxy ring opening and vicinal diacylation of epoxidized triglycerides in the canola oil. Sulfated‐ZrO₂ was prepared and characterized to measure the physico‐chemical properties required for the effective catalysis. The Taguchi (L16 orthogonal array) statistical design method was employed to optimize the process conditions for the maximum formation of diacylated canola oil. Sulfated‐ZrO₂ demonstrated promising activity for the epoxy ring opening and vicinal diacylation of canola oil, and 99 % conversion was achieved at the optimum process conditions of temperature 130 °C, epoxy to acetic anhydride molar ratio (1:1.25), 16 wt% of catalyst loading and reaction time of 1 h which were inferred from the Taguchi analyses. The products were characterized and confirmed with FT‐IR, ¹H NMR and sodium spray mass spectroscopy. Spectroscopic analysis also confirmed the absence of intermediate products. The statistical analyses was undertaken to determine the order, rank and interactions among the process variables. The reaction followed Langmuir–Hinshelwood–Hougen–Watson type mechanism and the kinetic data was fitted in overall second order equation. Calculated apparent activation energy was 23.1 kcal/mol.     

Polyester composite water uptake and organic contaminant release affected by carbon nanofiber reinforcements

The incorporation of carbon nanofiber (CNF) into glass fiber (GF) composites is a potential route to extend polymer composite service‐life and enhance mechanical properties. Under nonstatic conditions, only limited information concerning water uptake and contaminant release properties of nanocomposite materials is currently available. Polyester composites containing GF and oxidized CNF were immersed in water for 30 days under nominal pressure at 23 °C, below the polymer's glass‐transition temperature. Water was analyzed and changed every three days to simulate water chemistry regeneration similar to exposures in flowing systems. Composites with oxidized CNF had greater water sorption capacity and leaching rates than CNF‐free composites. The total mass of organic contaminant released correlated with the amount of water sorbed by each composite (r² = 0.91), although CNF dispersion was found to vary greatly within composites. The greatest and least contaminant release rates were found for the polyester‐CNF and the polyester‐GF composites, respectively. While volatile aromatic resin solvents and stabilizer compounds were detected, their concentrations declined over the 30 day exposure period. We hypothesize that the hydrophilic nature of the oxidized CNF increased the water sorption capacity of the polyester composites. Additional studies are warranted that examine the impact of this phenomenon on composite mechanical and long‐term durability properties. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43724.     

Visible Light Photocatalysis on Magnetically Recyclable Fe3O4/Cu2O Nanostructures

Catalysis Letters - Magnetically recyclable visible light photocatalysts for the degradation of critical organic pollutants are an urgent industrial requirement. Nonetheless, one component...     

Fabrication of Barium Strontium Titanate (Ba0.6Sr0.4 TiO3) 3D Microcomponents from Aqueous Suspensions

This study reports on the fabrication of BST (Ba_0.6Sr_0.4TiO₃)‐based 3D microcomponents through an aqueous colloidal approach. The BST powder was synthesized by solid‐state reaction assisted by thermal analysis and XRD diffraction. Well crystalline cubic BST single phase was obtained upon heat‐treating the precursor powder mixture at 1200°C–1250°C. The reactivity of the BST powder toward water was evaluated by the changes in pH and concentration of leached ionic species along aging time. Hydrolysis reactions were suppressed by chemisorbing a suitable phosphate‐based protective agent and enabled an excellent dispersion ability to be achieved. Aqueous suspensions with solids loadings as high as 50 vol% that are stable against hydrolysis for several days could easily be prepared from the surface‐treated BST powder in aqueous solutions of an epoxy resin. After adding a suitable hardener, the colloidal suspensions could easily be cast into soft silicon rubber molds to obtain homogeneous and high dense green BST bodies.     

Low Cost Porous Alumina with Tailored Microstructure and Thermal Conductivity Prepared using Rice Husk and Sucrose

This study demonstrates a cost‐effective way to fabricate porous ceramics with tailored porosity and pore microstructure using 5–40 wt% rice husk (RH) in <75 μm, 75–180 μm, 180–355 μm, 355–420 μm, and 420–600 μm size, as pore former. Sucrose, used as binder, also acted as a pore former. Porous alumina compacts with 20%–66% volume fraction porosity and 50–516 μm pore size (length) were successfully fabricated. Microstructure of samples reveal randomly oriented elongated coarse pores and fine pores (avg. size 4 μm), created during burnout of RH and sucrose, respectively. Samples with isolated and/or interconnected pores were fabricated using this process. Thermal conductivity of the samples prepared was measured using Transient Plane Source (TPS) technique. Thermal conductivity ranges from 1.2 to 24 W/mK. Experimental results agree closely with predictions made based on Effective Medium Theory (EMT) for a two‐phase system.