Estolides from meadowfoam oil fatty acids and other monounsaturated fatty acids

The formation of estolides was detected during the studies on dimerization of meadowfoam oil fatty acids. By adjusting the reaction conditions, it was possible to produce monoestolides with little dimer or trimer formations. Estolides have potential use in lubricant, cosmetic and ink formulations and in plasticizers. This paper reports the conditions for production of estolides from mixed meadow-foam fatty acids, commercial oleic acid, high-oleic sun-flower oil fatty acids,cis-5,cis-13-docosadienoic acid, petroselinic acid and linoleic acid.     

Elevated-Temperature-Delayed Failure of Alumina Reinforced with 20 vol% Silicon Carbide Whiskers

Alumina composites reinforced with 20 vol% SiC whiskers were exposed to applied stresses in four-point flexure at temperatures of 1000°, 1100°, and 1200°C in air for periods of up to 14 weeks. At 1000° and 1100°C, an "apparent" fatigue limit was established at stresses of ∼ 75% of the fast fracture strength. However, after long-term (>6 weeks) tests at 1100°C, some evidence of crack generation as a result of creep cavitation was detected. At 1200°C applied stresses as low as 38% of the 1200°C fracture strength were sufficient to promote creep deformation and accompanying cavitation and crack generation and growth resulting in failures in times of <250 h.     

Filtration in coal liquefaction: preparation of filter aid from filter cake

In this study the preparation of filter aid from filter cake is considered. Two methods of preparation, carbonization at 550–600 °C and combustion at 800–1000 °C, are used and the optimum conditions determined. The performance of the products is assessed as both a precoat and body feed by comparison with a commercial grade of diatomite. It is shown that efficient filter aids, with performances comparable to that of diatomite, may be produced from filter cake.     

Estimation of the concentration of donatable hydrogen in a coal solvent by n.m.r.

¹H and ¹³C nuclear magnetic resonance (n.m.r.) spectroscopies have been used to study the changes in composition of a hydrogenated anthracene oil solvent that occur during extraction of a UK bituminous coal. It has been shown that the principal hydrogen donor groups in the solvent are hydroaromatic and naphthenic rings in hydroaromatic species. Good agreement was achieved between the concentration of donatable hydrogen estimated from n.m.r., and the amount of hydrogen transferred from the solvent during exhaustive extraction.     

Providing lubricity in food fat systems

Lubricity, in particular mouthfeel, is an important factor in production of vegetable oil bases for food product formulations. Certain functional characteristics are necessary for good texture at various temperatures. These characteristics are dependent on degree of unsaturation, fatty acid distribution, and degree of geometrical isomerization during processing. Proper selectivity and activity of hydrogenation catalysts used in hardening of the oils are essential. Sufficient solid fat content must be balanced by necessary oxid ative stability. Products discussed include salad oils and their formulations in pourable and spoonable salad dressings, mayonnaises, frying oils, imitation dairy products, margarines and bakery shortenings. Past, present and future industry technology will be evaluated for each type of food fat product. Customer needs have greatly affected the course of research in this area.     

Comparative Assay of Antioxidant Packages for Dimer of Estolide Esters

A series of 26 different antioxidants and commercial antioxidant packages designed for petroleum‐based materials, containing both natural and synthetic‐based materials, were evaluated with dimeric coconut‐oleic estolide 2‐ethylhexyl ester (2‐EH), a bio‐based material. The different antioxidants were categorized into different classes of phenolic, aminic, and blended/others materials. The oxidation onset temperatures (OT) using non‐isothermal pressurized differential scanning calorimetry (PDSC) were measured and recorded under previously reported standard conditions. The aminic series gave the best resistance to oxidation as defined by the PDSC method with OT of 246.6 and 244.7 °C for the best two performers, which was a 38 °C improvement over the uninhibited or unformulated dimer estolide material. The phenolic series, containing most of the naturally occurring antioxidants, was the least successful formulation package for the dimer estolide. The blended/other materials, which were specifically designed for petroleum‐based lubricants, did not have the best OT, since the estolides and other bio‐based materials interact differently than their petroleum counterparts. A number of potential antioxidants have been identified as useful additives for the estolides esters. The OT of the estolide and formulated materials correlated well with other bio‐based materials such as biodiesel.     

An X-ray absorption spectroscopy study of Mo oxidation in Pb at elevated temperatures

The corrosion of fuel cladding and structural materials by lead and lead-bismuth eutectic in the liquid state at elevated temperatures is an issue that must be considered when designing advanced nuclear systems and high-power spallation neutron targets. In this work, lead corrosion studies of molybdenum were performed to investigate the interaction layer as a function of temperature by X-ray absorption spectroscopy. In situ X-ray absorption measurements on a Mo substrate with a 3-6 μm layer of Pb deposited by thermal evaporation were performed at temperatures up to 900 °C and at a 15° angle to the incident X-rays. The changes in the local atomic structure of the corrosion layer are visible in the difference extended X-ray absorption fine structure and the linear combination fitting of the X-ray absorption near-edge structure to as-deposited molybdenum sample and molybdenum oxide (MoO₂ and MoO₃) standards. The data are consistent with the appearance of MoO₃ in an intermediate temperature range (650-800 °C) and the more stable MoO₂ phase dominating at high and low temperatures.     

Chemometric profiling of pre-climacteric Sri Lankan mango fruit (Mangifera indica L.)

There is no published information on the genotypic variation of major biochemical constituents in mango fruit endemic to Sri Lanka. Accordingly, non-structural carbohydrates, non-volatile organic acids and total phenolics were determined from the peel and pulp of pre-climacteric Sri Lankan mango cultivars (viz. Willard, Karutha Colomban, Vellai Colomban, Ampalavi, and Malgova) at three different maturity stages. Principal components analysis revealed distinct clustering of samples according to their biochemical profiles of peel and pulp at three maturity stages. Sugar concentrations generally declined with maturity in both peel and pulp except for cv. Willard. Fructose was the predominant sugar in both peel (56.2–106 mg/g dry weight (DW)) and pulp (67.4–141 mg/g DW), followed by glucose and sucrose. Starch concentration increased with maturity and was higher in pulp (26.0–55.0% DW) than peel (18.2–38.9% DW) at full mature stage. Dry matter as a proportion of fresh weight (FW) increased with maturity.     

Improvement of fuel properties of cottonseed oil methyl esters with commercial additives

The low temperature operability and oxidative stability of cottonseed oil methyl esters (CSME) were improved with four anti‐gel additives as well as one antioxidant additive, gossypol. Low temperature operability and oxidative stability of CSME was determined by cloud point (CP), pour point (PP), cold filter plugging point (CFPP), and oxidative stability index (OSI). The most significant reductions in CP, PP, and CFPP in all cases were obtained with Technol®, with the average reduction in temperature found to be 3.9 °C. Gunk®, Heet®, and Howe's® were progressively less effective, as indicated by average reductions in temperature of 3.4, 3.0, and 2.8 °C, respectively. In all cases, the magnitude of CFPP reduction was greater than for PP and especially CP. Addition of gossypol, a polyphenolic aldehyde, resulted in linear improvement in OSI (R² = 0.9804). The OSI of CSME increased from 5.0 to 8.3 h with gossypol at a concentration of 1000 ppm.     

Does photoelectrocatalysis by TiO2 work?

BACKGROUND: This paper examines TiO₂ photoelectrocatalysis (PEC), a process that increases the efficiency of TiO₂ photocatalysis (PC) by applying a potential to separate the UV‐generated charge carriers whose recombination typically limits photonic efficiencies of conventional photocatalysis. RESULTS: Four representative photoelectrocatalytic reactions, nitrophenol oxidation, oxalate degradation, E. coli inactivation and dye decolouration were considered. For all four, a small applied potential raised the rate of pollutant removal by TiO₂ electrodes. Because the improvements were probably insufficient to make PEC technologically viable except in niche applications, rates of pollutant removal by PEC and by PC using TiO₂ particle dispersions were directly compared. PEC rates were not significantly larger than rates of PC by dispersions. CONCLUSION: Discussions of the implications of these conclusions focus on whether PEC is currently limited by reactor design (irradiation geometry, or mass transfer) or by electrode materials. It is inferred that the performance of present electrodes is not limited significantly by mass transfer constraints. Since the choice of electrode materials (sol–gel or thermal electrodes) has been shown to influence PEC efficiency, recent results on titania nanotubes (TNT) are reviewed. It is concluded that the enhancement factors—the PEC:PC ratio—of TNT electrodes are no higher than those of conventional materials. Copyright © 2011 Society of Chemical Industry