4.4 Article

The Use of Hydrothermal Carbonization to Recycle Nutrients in Algal Biofuel Production

期刊

ENVIRONMENTAL PROGRESS & SUSTAINABLE ENERGY
卷 32, 期 4, 页码 962-975

出版社

WILEY
DOI: 10.1002/ep.11812

关键词

hydrothermal carbonization; subcritical water hydrolysis; nutrient recycling; biodiesel; microalgae

资金

  1. NSF Graduate Research Fellowship
  2. University of Michigan Graham Environmental Sustainability Institute Fellowship
  3. University of Michigan College of Engineering
  4. U.S. National Science Foundation [CBET-1133439]
  5. Directorate For Engineering
  6. Div Of Chem, Bioeng, Env, & Transp Sys [1133439] Funding Source: National Science Foundation

向作者/读者索取更多资源

The high fertilizer demand for biodiesel production from microalgae is a significant challenge facing the commercialization of this promising technology. We investigated a processing strategy called hydrothermal carbonization (HTC) to convert wet algal biomass into a lipid-rich hydrochar and aqueous phase (AP) co-product. By reacting biomass at 200 degrees C for 15 min, about 50% of the algae biomass became a solid hydrochar and roughly 40-70% of the C, N, and P in the reactant material dissolved into the AP. For the first time, an AP co-product of this nature was analyzed by HPLC, GC-MS and FT-ICR-MS to identify and characterize the dissolved organic matter. Using a unique marine bi-culture suspected to contain a green algae (Nannochloris) and a cyanobacteria (Synechocystis), we demonstrated that this AP co-product can support biomass growth better than a medium containing only inorganic nutrients. To manage unwanted contamination and optimize AP utilization, we employed a two-stage growth process and fed-batch additions of the AP co-product. The effect of media recycling and nutrient supplementation, as well as a production model for a large-scale facility, are discussed. Our work suggests that HTC can play a critical role in making algal biorefineries more sustainable by obviating biomass drying for fuel processing and recycling nutrients. (c) 2013 American Institute of Chemical Engineers Environ Prog, 32: 962-975, 2013

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