Single-stage cocurrent dilute acid pretreatments were carried out on yellow poplar (Liriodendron tulipifera) sawdust using an as-installed and short residence time modified pilot-scale Sunds hydrolyzer and a 4-L bench-scale NREL
digester (steam explosion reactor). Pretreatment conditions for the Sunds hydrolyzer, installed in the NREL process development
unit (PDU), which operates at 1 t/d (bone-dry t) feed rate, spanned the temperature range of 160 – 210°C, 0.1 – 1.0% (w/w)
sulfuric acid, and 4-10-min residence times. The batch pretreatments of yellow poplar sawdust in the bench-scale digester
were carried out at 210 and 230°C, 0.26% (w/w) sulfuric acid, and 1-, 3-, and 4-min residence times. The dilute acid prehydrolysis
solubilized more than 90% of the hemicellulose, and increased the enzymatic digestibility of the cellulose that remained in
the solids. Compositional analysis of the pretreated solids and liquors and mass balance data show that the two pretreatment
devices had similar pretreatment performance. 相似文献
Applied Biochemistry and Biotechnology - The enzymatic digestibility of a pretreated substrate is enhanced by increasing the severity of the pretreatment conditions, apparently because a greater... 相似文献
The critical exponents , and of undeuterated and partially deuterated ferroelectric betaine arsenate are estimated. Small but remarkable deviations from the tricritical values are observed. The obtained values are tested via scaling of the isothermals.At some distance aboveTc a cross-over of the effective critical exponent to a value typically for short-range forces is observed. A suitably defined cross-over temperature range decreases with increasing deuteration and seems to vanish near the antiferroelectric phase boundary. 相似文献
The Solar Energy Research Institute (SERI) recently completed a detailed engineering and economic analysis of the simultaneous saccharification and fermentation (SSF) based wood-to-ethanol process. The reference-case design was based on a plant capacity of 1920 dry t/d and a wood cost of $42/dry t. For this case, the preliminary estimate of the production cost of the ethanol product is about $1.22/gal. The combined effects of optimizing SSF enzyme loading, increasing plant capacity to 10,000 dry t/d, and reducing wood cost to $34/dry t are to reduce the preliminary estimate of the production cost to about $0.95/gal. Other technological improvements may further reduce the production cost. Certain technical assumptions, inherent in the analysis, are being investigated further.
Porous sol-gel glasses, either impregnated with pure C60 or doped with a methanofullerene derivative, have been studied and induced absorption or reverse saturable absorption (RSA) has been observed in both types of solid materials. The samples impregnated by pure C60 mainly contain well-dispersed fullerene molecules. Unlike crystalline films of C60, their absorption dynamics can be well described by a 5-level model, developed for non-interacting C60-molecules in solutions. Methanofullerene samples, on the other hand, show signs of micellar aggregation and therefore RSA dynamics that are influenced by solid state effects. We observe an important decrease of transmission at high fluences for both kinds of samples, a shortened singlet-state lifetime to that observed in solution, but nonetheless, a triplet yield, that cannot be considered as negligible. In the case of pure C60 in a sol-gel matrix, we can explain the faster de-excitation dynamics, relative to behavior in solution, mainly by the absence of stabilizing aromatic solvents and also by the interaction of the amorphous environment with the molecules. Concerning the methanofullerene samples, the acceleration of the de-excitation dynamics can be principally attributed to solid-state effects due to the micellar aggregation. 相似文献
Selective thinning of forests in the western United States will generate a large, sustainable quantity of softwood residues
that can be an attractive feedstock for fuel ethanol production. The major species available from thinning of forests in northern
California and the eastern Rocky Mountains include white fir (Abies concolor), Douglas fir (Pseudotsuga menziesii), and Ponderosa pine (Pinus ponderosa). Douglas fir chips were soaked in 0.4% sulfuric acid solution, then pretreated with steam at 200 – 230°C for 1 – 5 min.
After pretreatment, 90 – 95% of the hemicellulose and as much as 20% of the cellulose was solubilized in water, and 90% of
the remaining cellulose can be hydrolyzed to glucose by cellulase enzyme. The prehydrolysates, at as high as 10% total solid
concentration, can be readily fermented by the unadapted yeastSaccharomyces cerevisiae D5A. 相似文献
Recently we had need for large quantities of N-benzoyl-4-oxo-1,2,3,4-tetrahydropyridine (1), its ethylene ketal derivative 7, and potentially other N-acyl derivatives. Prior to our initial studies, the N-carboethoxy derivative 2 had been prepared by sodium borohydride reduction of N-carboethoxy-4-pyridone.1. 相似文献
With the formation of novel organometallic macromolecules in mind, the polycondensation of transition metal ions and bridged cyclopentadienyl ligands was studied. To this end solvated salts MX2 (M = Fe, Ni, and Cr) were treated with a ligand that consisted of two doubly silyl-bridged cyclopentadienyl anions. For M = Fe and diluted solutions a series of rings Oi was obtained that consisted of a minimum of six (O6) and up to 17 (O17) ferrocene moieties in the backbone. They were separated partly by medium pressure liquid chromatography. The macrocycles were established by high-resolution MALDI-TOF mass spectroscopy which also yielded the molecular weight, the polydispersion, and the mean ring size, chi n, of the mixture of reaction products. When the reaction temperature was decreased from 25 degrees C to -20 degrees C, chi n increased from 8.1 to 10.8. Ferrocene-containing chains, lambda j, with 2 < or = j < or = 12 were obtained in addition to rings in the presence of water; the terminal groups were cyclopentadiene moieties. The reaction of two ferrocene-fused cyclopentadienyl anions with [FeCl2(thf)1.5] gave chains consisting of exclusively uneven numbers of ferrocenes. For M = Ni and Cr the formation of doubly silyl-bridged nickelocenes and chromocenes was proven by NMR spectroscopy. MALDI-TOF mass spectroscopy showed nickelocene-containing chains accompanied by some rings. For M = Fe the H,H-DQF COSY spectra established the structure of O7, O8, and O9. The oxidation of the ferrocene-containing ring O7 with I2, NOPF6, and AgPF6 gave ionic species [O7]n+ which suffered from low stability. The ring-closing reaction is discussed, and the relative abundance of the various rings is related to MNDO calculations. 相似文献