Plumbago zeylanica (known as "Chitrak") is a useful Indian medicinal plant. The root of the plant and its constituents are credited with potential therapeutic properties including anti-atherogenic, cardiotonic, hepatoprotective and neuroprotective properties. To examine possible mechanisms of action of P. zeylanica (Chitrak), in relation to its reported beneficial properties, antioxidant effects of the aqueous/alcoholic extracts of root, corresponding to medicinal preparations, and the active ingredient, plumbagin, were studied. Methods used included: ferric reducing/antioxidant power (FRAP), radical scavenging of 1,1-diphenyl-2-picryl hydrazyl (DPPH) and 2,2'-azobis-3-ethylbenzthiazoline-6-sulfonic acid (ABTS), lipid peroxidation in rat liver mitochondria induced by different agents, and estimating phenolic and flavonoid content. In FRAP/DPPH assays, boiled ethanolic extracts were the most effective, while in the ABTS assay boiled aqueous extracts were the most efficient. These extracts also significantly inhibited lipid peroxidation induced by cumene hydroperoxide, ascorbate-Fe(2+) and peroxynitrite and contained high amounts of polyphenols and flavonoids. To examine the mechanisms of action in detail, antioxidant and pulse radiolysis studies with plumbagin were conducted. The hydroxyl (.OH), alkyl peroxyl (CCl(3)OO.), linoleic acid peroxyl (LOO.), and glutathiyl (GS.) radicals generate a phenoxyl radical upon reaction with plumbagin. The bimolecular rate constants were: .OH, 2.03 x 10(9) dm(3)mol(-1)s(-1); CCl(3)OO., 1.1 x 10(9) dm(3)mol(-1)s(-1); LOO., 6.7 x 10(7) dm(3)mol(-1)s(-1); and GS., 8.8 x 10(8) dm(3)mol(-1)s(-1). In conclusion, our studies reveal that extracts of P. zeylanica and its active ingredient plumbagin have significant antioxidant abilities that may possibly explain some of the reported therapeutic effects.
An abundant, low-cost, and high-quality supply of lignocellulosic feedstock is necessary to realize the large-scale implementation of biomass conversion technologies capable of producing renewable fuels, chemicals, and products. Barriers to this goal include the variability in the chemical and physical properties of available biomass, and the seasonal and geographic availability of biomass. Blending several different types of biomass to produce consistent feedstocks offers a solution to these problems and allows for control over the specifications of the feedstocks. For thermochemical conversion processes, attributes of interest include carbon content, total ash, specific inorganics, density, particle size, and moisture content. In this work, a series of switchgrass and pine residues blends with varying physical and chemical properties were evaluated. Physical and chemical properties of the pure and blended materials were measured, including compositional analysis, elemental analysis, compressibility, flowability, density, and particle size distribution. To screen blends for thermochemical conversion behavior, the analytical technique, pyrolysis gas chromatography mass spectrometry (Py-GC/MS), was used to analyze the vapor-phase pyrolysis products of the various switchgrass/pine residues blends. The py-GC/MS findings were validated by investigating the bio-oils produced from the selected blends using a lab-scale fluidized-bed pyrolysis reactor system. Results indicate that the physical properties of blended materials are proportional to the blend ratio of pure feedstocks. In addition, pyrolysis of pine residues resulted in bio-oils with higher carbon content and lower oxygen content, while switchgrass derived pyrolysis products contained relatively greater amount of anhydrosugars and organic acids. The distribution of the pyrolysis vapors and isolated bio-oils appear to be a simple linear combination of the two feedstocks. The concentration of alkali and alkaline Edmunds et al.Blended Feedstocks for Thermochemical Conversion earth metals (Ca, K, Mg, and Na) in the blended feedstocks were confirmed to be a critical parameter due to their negative effects on the bio-oil yield. This work demonstrates that blending different sources of biomass can be an effective strategy to produce a consistent feedstock for thermochemical conversion.
Three-dimensional (3D) printing is a revolutionary manufacturing technique that can fabricate a 3D object by depositing materials layer by layer. Different materials such as metals, polymers, and concretes are generally used for 3D printing. In order to make 3D printing sustainable, researchers are working on the use of different bioderived materials for 3D printing. Because of the abundant and sustainable sources, and versatile properties, biomaterials are considered as the potential candidates that have the ability to replace petroleum-based polymers. This review highlights the basic overview of fused deposition modeling (FDM) technique of 3D printing and recent developments that have occurred on FDM printing using biomaterials. Specifically, FDM printing process, final properties, and characteristics of biopolymers, their composites, and polymers containing biofillers are discussed.
pH control has been essential for butanol production with Clostridium acetobutylicum. However, it is not very clear at what pH level the acid crash will occur, at what pH level butanol production will be dominant, and at what pH level butyric acid production will be prevailing. Furthermore, contradictory results have been reported about required acidic conditions for initiation of solventogenesis. In this study, with the aim of further understanding the role of undissociated butyric acid in butanol production, we investigated the correlation between undissociated butyric acid concentration and specific butanol production rate in batch fermentation of Clostridium acetobutylicum by comparing three pH control approaches: NaOH neutralization (at 12, 24 or 36 h), CaCO3 supplementation (2, 5, or 8 g/l) and NaOAc buffering (pH 4.6, 5.0 or 5.6). By neutralizing the fermentation pH to ~5.0 at different time, we observed that neutralization should take place at the beginning of exponential phase (12 h), and otherwise resulting in lower concentrations of undissociated butyric acid, cell biomass and final butanol. CaCO3 supplementation extended cell growth to 36 h and resulted in higher butyrate yield under 8 g/L of CaCO3. In the NaOAc buffering, the highest specific butanol rate (0.58 h−1) was associated with the highest undissociated butyric acid (1.92 g/L). The linear correlation of the undissociated butyric acid with the specific butanol production rates suggested the undissociated butyric acid could be the major driving force for butanol production.
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