Biobutanol: science,engineering, and economics

Among several liquid alternative fuels, biobutanol has shown great promise because of its very similar properties to gasoline. This review provides an overview of research activities in acetone–butanol–ethanol (ABE) fermentation over the past two and a half decades. We have addressed seven important facets of ABE fermentation, viz. biochemistry, microbial cultures, alternative substrates, solvent recovery, fermentation mode and reactor designs, mathematical modeling, and economics. Development of mutant strains having higher yield, selectivity and tolerance to inhibition, and search for cheap alternative substrates for fermentation are most important thrust areas in biobutanol production. New and efficient processes have been developed for in situ removal and recovery of the ABE solvents. Several rigorous kinetic and physiological models for fermentation have been formulated, which form useful tool for optimization of the process. These research activities have been reviewed in this paper. Finally, we have summarized studies on the economic viability of large‐scale ABE fermentation processes employing various process designs, substrates, and microbial cultures. With the use of new strains, inexpensive substrates, and superior reactor designs, economic potential of ABE fermentation has been found to be highly attractive. Research efforts in science, engineering, and economics of ABE fermentation have brought biobutanol close to commercialization as liquid alternate fuel. Copyright © 2011 John Wiley & Sons, Ltd.     

Effect of Long-Term Thermal Exposures on Microstructure and Impression Creep in 304HCu Grade Austenitic Stainless Steel

Metallurgical and Materials Transactions A - This paper presents the results of microstructural evolution and mechanical properties in 304H Cu grade austenite stainless (SS 304HCu) during long-term...     

Computational study of 5<Emphasis Type="Italic">d</Emphasis> transition metal mononitrides and monoborides using density functional method

5d-metal mononitrides and monoborides viz. X-N and X-B (X = La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Hg) are studied using density functional method based B3LYP functional with LANL2DZ and SDD basis set. The lowest spin state, electron affinities, ionization potentials and binding energies for mononitrides and monoborides are obtained. The electronic state and electronic configuration of mononitrides and monoborides are discussed. Orbitals involved in bond formation are identified. The properties of mononitrides and monoborides are compared. It is found that 5d-metal atoms form stronger bond with nitrogen atom than the boron atom. The range of binding energy, electron affinity and ionization potential is wider for mononitrides than that for monoborides. The properties of 5d-metal mononitrides and 3d-metal mononitrides are also compared. The binding energies for the former are lower than those for the latter.     

Synthesis and characterization of novel poly(aniline-co-m-aminoacetophenone) copolymer nanocomposites using dodecylbenzene sulfonic acid as a soft template

A series of dodecylbenzene sulphonic acid (DBSA) doped poly(aniline-co-m-aminoacetophenone) copolymer composites of different compositions were synthesized in micellar solution of DBSA to obtain nanosphere morphology with enhanced processability. The plausible mechanism for the formation of poly(aniline-co-m-aminoacetophenone)-DBSA copolymer composite has been presented. These DBSA doped copolymer composites were characterized by UV–Visible, FTIR spectroscopy and XRD analysis techniques. UV–Vis absorption spectrum of the composites showed 325 and 637 nm which corresponds to the π–π* and n–π* transition. In FTIR spectroscopy a broad band around 2,924 cm^?1 corresponds to C–H vibration of DBSA indicating good agreement with the characteristic bands of DBSA. The sharp band at 1,292 cm^?1 is assigned to C–N stretching mode of vibration of N–Ph–N units. The X-ray diffraction of composites reveals that these composites are amorphous in nature. The number of diffraction peaks decreased with increase in the m-aminoacetophenone content. It indicates that these composites are amorphous in nature. Morphological studies (SEM) reveal that these composites have a spherical morphology with the average size of 100–200 nm. These composites exhibit electrical conductivity value of 0.744 × 10^?3 S/cm and enhanced solubility than polyaniline. Moreover, at the presented work, the DBSA doped copolymer composites were obtained in high yields by keeping an oxidant to co-monomer ratio of 1:1.     

An optimized pretreatment method in the analysis of negative plate of lead acid battery

The composition of the plate in lead acid battery plays a vital role on battery performance. Therefore, controlling and monitoring of plate composition is utmost important in order to attain required battery performance. While monitoring negative plate, it has to be ensured that they are not exposed to air, which would otherwise result in Pb oxidation; thereby affecting the accuracy of the test data. Nevertheless, published information is scarce on the “pretreatment and preservation of the negative plates”. The objective of this study is to develop a suitable procedure to “preserve and pretreat the negative plate” prior to chemical composition analysis. A host of experimental parameters like immersion time in water, effect of drying reagent and air drying time were studied. Two drying solvents; namely, methanol and acetone were studied to evaluate their suitability.     

Studies on polyurethanes and polyurethane–ureas derived from divalent metal salts of mono(hydroxybutyl) hexolate

Divalent metal salts of mono(hydroxybutyl)hexolate [M(HBH)₂), M=Ca²⁺, Mn²⁺or Pb²⁺] were synthesized by the reaction of 1,4‐butanediol, 5,6,7,8,10,10‐hexachloro‐3a,4,4a,5,8,8a,9,9a‐octahydro‐5,8‐methanonaphtho‐[2,3‐C]‐furan‐1,3‐dione and divalent metal acetates. Hexamethylene bis [N′‐(1‐hydroxy‐2‐methyl‐prop‐2‐yl)urea] (HBHMPU) and tolylene 2,4‐bis[N ′‐(1‐hydroxy‐2‐methyl‐prop‐2‐yl)urea] (TBHMPU) were synthesized by reacting 2‐amino‐2‐methyl‐propan‐1‐ol with hexamethylene diisocyanate (HMDI) and tolylene 2,4‐diisocyanate (TDI), respectively, in toluene solvent. Flame‐retardant metal‐containing polyurethanes were synthesized by the solution polymerization of HMDI with M(HBH)₂ and the polyurethane–ureas by reacting HMDI with 1:1 mixture of M(HBH)₂ and HBHMPU or TBHMPU, respectively, in DMSO as solvent. The polymers have been characterized by elemental analysis, solubility, viscosity and IR and ¹H NMR spectroscopy. The thermal stability of the polymers has been studied by thermogravimetry. The flame‐retardant property of the polymers has been investigated by measuring limiting oxygen index values. © 2000 Society of Chemical Industry     

Microwave-assisted route for synthesis of nanosized metal oxides

Microwave-assisted route for the synthesis of nanomaterials has gained importance in the field of synthetic technology because of its faster, cleaner and cost effectiveness than the other conventional and wet chemical methods for the preparation of metal oxide nanoparticles. In the present work, synthesis of metal oxide nanoparticles viz., γ-Fe₂O₃, NiO, ZnO, CuO and Co-γ-Fe₂O₃ were carried out by microwave-assisted route through the thermal decomposition of their respective metal oxalate precursors employing polyvinyl alcohol as a fuel. The metal oxide nanoparticles are then characterized for their size and γ to α (in γ-Fe₂O₃) transition and structure by employing powder X-ray diffraction (XRD) pattern, high-temperature X-ray diffraction (HTXRD) pattern and Fourier transform infrared (FT-IR) spectral studies. The morphology of the samples ranged from nanorods to irregular-shaped particles for different metal oxide samples on the basis of scanning electron microscopy and transmission electron microscopy images. Frequency-dependent dielectric study of the ferrite samples (γ-Fe₂O₃ and Co-Fe₂O₃) showed a similar behaviour, where the dielectric constant decreased rapidly with increase in frequency. Possible explanation for this behaviour is given.     

Impression Creep Behavior of 316LN Stainless Steel

Impression creep tests have been carried out at 923 K on 316LN SS containing 0.07, 0.14, and 0.22 wt.% nitrogen, under different applied stress levels. It was observed that the impression creep depth versus time curves were similar to the creep curves obtained from conventional uniaxial creep tests. The impression creep curves were characterized by a loading strain and primary and secondary creep stages similar to uniaxial creep curves. The tertiary stage observed in uniaxial creep curves was absent. The steady-state impression velocity was found to increase with increasing applied stress. The equivalent steady-state creep rates calculated from impression velocities were found to be in good agreement with the steady-state creep rates obtained from conventional uniaxial creep tests. Equivalence between applied stress and steady-state impression velocity with uniaxial creep stress and steady-state creep rate, respectively, has been established based on the laws of mechanics for time-dependent plasticity. It was found that impression velocity was sensitive to the variation in nitrogen content in the steel; impression velocity decreased with increasing nitrogen content, and the results obtained in this study were in agreement with those obtained from uniaxial creep tests.