Search

The detonation propagation characteristics of the mixtures, 2H 2 + O 2 +3Ar and CH 4 + 2O 2 , were investigated. Accordingly, the mixtures were tested in round tube with inner diameter of D = 80 mm and annular tubes with widths of w = 25 mm, 15 mm, and 5 mm. The two mixtures represent stable mixture with regular cell pattern and unstable mixture with irregular cell pattern, respectively. Smoked foils were utilized to record cellular structure under various initial conditions. Subsequently, the length scale L dsc was measured, which represents the length from the start of the test section to the position where the cellular structure changes drastically (the cell size obviously increases or the structure disappears). The results reveal that both mixtures can successfully propagate in round tube and annular tubes of 25 mm and 15 mm, but fail in 5 mm annular tube. The L dsc value of 2H 2 + O 2 + 3Ar is higher than that of CH 4 + 2O 2 in 80 mm and 15 mm tubes, but it is opposite in 25 mm tube. Moreover, the relationship between L dsc and hydraulic diameter D H was analysed. For a given tube, the values of L dsc and L dsc / D H increased when the initial pressure increased. And the variation trend of L dsc and L dsc / D H of CH 4 + 2O 2 is steeper. Furthermore, the mixtures 2H 2 + O 2 + 3Ar and CH 4 + 2O 2 resulted in over-driven detonation in 15 mm and 25 mm annular tubes, respectively. The ratio between the total reaction length (sum of the induction length and exothermic length) and the hydraulic diameter (D H /(Δ i + Δ e)) correspond to critical values of 18 for hydrogen-oxygen-argon and 6 for methane-oxygen, below which the detonation will fail. [ABSTRACT FROM AUTHOR]

Microalgae are promising feedstock for renewable fuels. The accumulation of oils in microalgae can be enhanced by nanoparticle exposure. However, the nanoparticles employed in previous studies are mostly non-biodegradable, which hinders nanoparticles developing as promising approach for biofuel production. We recently reported the engineered resin nanoparticles (iBCA-NPs), which were found to be biodegradable in this study. When the cells of green microalga Chlamydomonas reinhardtii were exposed to the iBCA-NPs for 1 h, the cellular triacyclglycerols (TAG) and starch contents increased by 520% and 60% than that in the control. The TAG production improved by 1.8-fold compared to the control without compromised starch production. Additionally, the content of total fatty acids increased by 1.3-fold than that in control. Furthermore, we found that the iBCA-NPs addition resulted in increased cellular reactive oxygen species (ROS) content and upregulated the activities of antioxidant enzymes. The relative expressions of the key genes involved in TAG and starch biosynthesis were also upregulated. Overall, our results showed that short exposure of the iBCA-NPs dramatically enhances TAG and starch accumulation in Chlamydomonas, which probably resulted from prompt upregulated expression of the key genes in lipid and starch metabolic pathways that were triggered by over-accumulated ROS. This study reported a useful approach to enhance energy-rich reserve accumulation in microalgae. Key points: 1. The first attempt to increase oil and starch in microalgae by biodegradable NPs. 2. The biodegradability of iBCA-NPs by the BOD test was more than 50% after 28 days. 3. The iBCA-NPs induce more energy reserves than that of previously reported NPs. [ABSTRACT FROM AUTHOR]

Microalgae are eukaryotic photosynthetic micro-organisms that convert CO 2 into carbohydrates, lipids, and other valuable metabolites. They are considered promising chassis for the production of various bioproducts, including fatty acid–derived biofuels. However, algae-based biofuels are not yet commercially available, mainly because of their low yields and high production cost. Optimizing strains to improve lipid productivity using the principles of synthetic biology should help move forward. This necessitates developments in the following areas: (1) identification of molecular bricks (enzymes, transcription factors, regulatory proteins etc.); (2) development of genetic tools; and (3) availability of high-throughput phenotyping methods. Here, we highlight the most recent developments in some of these areas and provide examples of the use of genome editing tools to improve oil content. [ABSTRACT FROM AUTHOR]