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Organic Fuels (organic + fuel)

Distribution by Scientific Domains

Chemistry	75%

Selected Abstracts

Application of New Organic Fuels in the Direct MgAl2O4 Combustion Synthesis

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 6 2008
Robert Iano
Abstract The paper presents a new version of MgAl2O4 solution-combustion synthesis, based on the individual reactivity of Mg(NO3)2 and Al(NO3)3 with respect to various fuels. Beside the traditionally used fuels (urea, glycine, ,-alanine), new organic reducing agents [monoethanolamine, triethanolamine, tris(hydroxymethyl)aminomethane and triethylenetetramine] have also been used. The study of the individual reactivities of Mg(NO3)2 and Al(NO3)3 with respect to each of the previously mentioned fuels suggested that there is a predilection of the two metal nitrates for certain fuels: urea is the optimum fuel for Al(NO3)3, whereas monoethanolamine represents the most suitable fuel for Mg(NO3)2. It has been shown by X-ray diffraction and thermal analysis that the use of a single fuel in the MgAl2O4 low-temperature combustion synthesis leads to the formation of an amorphous powder. In this case, the formation of pure crystalline MgAl2O4 requires a subsequent thermal treatment at 900 °C with 1 h soaking time. On the other hand, the use of fuel mixtures containing urea and monoethanolamine or urea and ,-alanine proved to be the rational solution for the direct formation of MgAl2O4. It has been shown that, by using the above-mentioned fuel mixtures, one can obtain pure nanocrystalline MgAl2O4 straight from the combustion reaction, no additional calcination being necessary. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source]

Structure of nanoporous zirconia-based powders synthesized by different gel-combustion routes

JOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 2007
Jorge R. Casanova
Zirconia-based ceramics that retain their metastable tetragonal phase at room temperature are widely studied due to their excellent mechanical and electrical properties. When these materials are prepared from precursor nanopowders with high specific surface areas, this phase is retained in dense ceramic bodies. In this work, we present a morphological study of nanocrystalline ZrO2,2.8 mol% Y2O3 powders synthesized by the gel-combustion method, using different organic fuels , alanine, glycine, lysine and citric acid , and calcined at temperatures ranging from 873 to 1173,K. The nanopore structures were investigated by small-angle X-ray scattering. The experimental results indicate that nanopores in samples prepared with alanine, glycine and lysine have an essentially single-mode volume distribution for calcination temperatures up to 1073,K, while those calcined at 1173,K exhibit a more complex and wider volume distribution. The volume-weighted average of the nanopore radii monotonically increases with increasing calcination temperature. The samples prepared with citric acid exhibit a size distribution much wider than the others. The Brunauer,Emmett,Teller technique was used to determine specific surface area and X-ray diffraction, environmental scanning electron microscopy and transmission electron microscopy were also employed for a complete characterization of the samples. [source]

Further uses of the heat of oxidation in chemical hazard assessment

PROCESS SAFETY PROGRESS, Issue 1 2003
Laurence G. Britton
Flammability: The "net heat of oxidation" technique described in an earlier publication is extended to predicting the lower flammable limits, lower limit flame temperatures, and limiting oxygen concentrations of chlorinated organic fuels having H:Cl ratios greater than unity. A new Rule is derived for predicting the effect of initial temperature on the lower flammable limits and limiting oxygen concentrations of organic fuels. It is suggested that this Rule be used in preference to the modified "Burgess-Wheeler" Rule. The effect of initial pressure is discussed. Instability: Net heats of oxidation (kcal/mol oxygen) for a series of disparate fuel groups are compared with ",HD," the maximum heat of decomposition (cal/g) calculated using CHETAH methodology. Given the reasonable assumption that CHETAH's "maximum heat of decomposition" cannot exceed the net heat of combustion ",HC," examination is made as to whether the ratio of these parameters (each expressed in units of kcal/mol), coined the "Reaction Heat Ratio" (RH), provides a useful new indicator for instability assessment. Of these parameters, the net heat of oxidation (,HC/S) is the best indicator to help assign NFPA Instability Ratings. However, ,HC/S cannot generally be used to assign ratings for organo-peroxides. Also, its performance as an indicator for hazardous polymerization depends on the ,HC/S difference between the reacting monomer and the polymer product, so it should become increasingly unreliable as the monomer ,HC/S approaches -100 kcal/mol oxygen. The ranking method tacitly assumes organic polymers to have a constant heat of oxidation of about -100 kcal/mol oxygen. Errors in this assumption must invalidate the ranking approach where ,HC/S differences are small. Finally, separate "cut-offs" must be used at each NFPA Instability Rating for organo-nitrates versus other organics containing combinations of CHON atoms. Additional materials need to be examined to extend this preliminary analysis. The net heat of oxidation would be a useful additional output parameter of the CHETAH program, if only for its application in flammability assessment. No conclusions are drawn regarding the usefulness of net heat of oxidation or RH in conducting CHETAH hazard assessments, since this procedure requires consideration of several variables. However, the analysis may be helpful to the ASTM E 27.07 subcommittee responsible for developing the program. For example, the -,HD , 700 cal/g cut-off used to assign a "high" CHETAH hazard rating typically corresponds to organic materials rated NFPA 1, the second to lowest hazard rating. [source]

Potential Synergies and Challenges in Refining Cellulosic Biomass to Fuels, Chemicals, and Power

BIOTECHNOLOGY PROGRESS, Issue 2 2003
Charles E. Wyman
Lignocellulosic biomass such as agricultural and forestry residues and dedicated crops provides a low-cost and uniquely sustainable resource for production of many organic fuels and chemicals that can reduce greenhouse gas emissions, enhance energy security, improve the economy, dispose of problematic solid wastes, and improve air quality. A technoeconomic analysis of biologically processing lignocellulosics to ethanol is adapted to project the cost of making sugar intermediates for producing a range of such products, and sugar costs are predicted to drop with plant size as a result of economies of scale that outweigh increased biomass transport costs for facilities processing less than about 10,000 dry tons per day. Criteria are then reviewed for identifying promising chemicals in addition to fuel ethanol to make from these low cost cellulosic sugars. It is found that the large market for ethanol makes it possible to achieve economies of scale that reduce sugar costs, and coproducing chemicals promises greater profit margins or lower production costs for a given return on investment. Additionally, power can be sold at low prices without a significant impact on the selling price of sugars. However, manufacture of multiple products introduces additional technical, marketing, risk, scale-up, and other challenges that must be considered in refining of lignocellulosics. [source]