2012
DOI: 10.4155/bfs.12.63
|View full text |Cite
|
Sign up to set email alerts
|

Energy innovation potential of oleaginous microalgae

Abstract: Algae have contributed greatly to the creation of the Earth's environment and the development of human civilization. Currently, microalgae are considered to be among the most promising sources for biofuel. Most microalgae accumulate triacylglycerols; however, fatty acid methyl esters produced from triacylglycerols by transesterification have critical end-use issues. Hydrocarbons produced by Botryococcus and Aurantiochytrium are the most suitable algal oils for replacing existing transportation fuels and are hi… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
34
0

Year Published

2013
2013
2024
2024

Publication Types

Select...
5
2

Relationship

1
6

Authors

Journals

citations
Cited by 52 publications
(34 citation statements)
references
References 82 publications
0
34
0
Order By: Relevance
“…177 Terpenes are polymers of isoprene C 5 H 8 . 179,180 Two metabolic pathways are capable of producing the isoprenoid building blocks, isopentenyl pyrophosphate and dimethylallyl diphosphate: the mevalonate (MVA) pathway and the methylerythritol phosphate (MEP) pathway, also known as the 1-deoxy-d-xylulose-5-phosphate pathway and the nonmevalonate pathway. The name "terpene" is derived from the word "turpentine."…”
Section: Terpene-based Biofuelsmentioning
confidence: 99%
“…177 Terpenes are polymers of isoprene C 5 H 8 . 179,180 Two metabolic pathways are capable of producing the isoprenoid building blocks, isopentenyl pyrophosphate and dimethylallyl diphosphate: the mevalonate (MVA) pathway and the methylerythritol phosphate (MEP) pathway, also known as the 1-deoxy-d-xylulose-5-phosphate pathway and the nonmevalonate pathway. The name "terpene" is derived from the word "turpentine."…”
Section: Terpene-based Biofuelsmentioning
confidence: 99%
“…Moreover, the ratio of n-C 15 H 32 in the total C 15 hydrocarbons was much higher than the ratio of n-C 16 H 34 in the total C 16 hydrocarbons ( Figure 8B). Thus, Reaction (7) was the main decarboxylation reaction (as compared to Reaction (8) Figure 10 shows the dependence of C15H31COOC16H33 conversion and C10-C16 hydrocarbon yield on reaction temperature for the catalytic deoxygenation of C15H31COOC16H33 in N2 atmosphere, for 2 h, over the 1 wt.% Pd/Mg(Al)O catalyst. C15H31COOC16H33 conversion increased with an increasing reaction temperature from 275 to 375 °C, and achieved a conversion of over 99% for the reaction at 375 °C for 2 h. The yield of C10-C16 hydrocarbons increased with an increasing reaction temperature from 275 to 325 °C.…”
Section: Catalytic Deoxygenation Of C15h31cooc16h33 In N2 Atmospherementioning
confidence: 99%
“…Moreover, the ratio of n-C15H32 in the total C15 hydrocarbons was much higher than the ratio of n-C16H34 in the total C16 hydrocarbons ( Figure 8B). Thus, Reaction (7) was the main decarboxylation reaction (as compared to Reaction (8)) in the catalytic deoxygenation of C15H31COOC16H33 in N2 atmosphere.…”
Section: Catalytic Deoxygenation Of C15h31cooc16h33 In N2 Atmospherementioning
confidence: 99%
See 2 more Smart Citations