Combined hydrothermal carbonization and gasication of biomass with carbon capture B. Erlach * , B. Harder, G. Tsatsaronis Technische Universität Berlin, Institute for Energy Engineering, Marchstr 18, 10587 Berlin, Germany article info Article history: Received 31 August 2011 Received in revised form 20 January 2012 Accepted 22 January 2012 Available online 20 February 2012 Keywords: Hydrothermal carbonization Biocoal Biomass upgrading Gasication BECCS Exergy analysis abstract Bio-energy with carbon capture and storage (BECCS) can result in negative net carbon emissions and may therefore provide an important technology option for meeting current greenhouse gas stabilization targets. To this end, syngas from biomass gasication combined with pre-combustion carbon capture can be used to produce either biofuels or electricity. Pre-treating the biomass with hydrothermal carbon- ization (HTC) produces a coal-like substance, biocoal, which is potentially better suited for entrained ow gasication than raw biomass. This paper compares HTC followed by entrained ow gasication of the biocoal with uidized bed gasication of raw wood, both with carbon capture and storage (CCS). Simulation studies undertaken with Aspen Plus are interpreted using exergy analysis. Syngas production is more efcient from biocoal than from raw wood but the conversion losses in the HTC process outweigh the efciency gains in the gasication. Carbon losses through gaseous and dissolved byproducts in the HTC also limit the capture rate. A CCS-IGCC with uidized bed gasication using raw wood results in an electrical efciency of 28.6% (HHV) and a carbon capture rate of 84.5%, while the conversion chain of HTC and a CCS-IGCC with entrained ow gasication yields an electrical efciency of 27.7% and a capture rate of 72.7%. Ó 2012 Elsevier Ltd. All rights reserved. 1. Introduction Syngas from biomass gasication is widely discussed as an intermediate feedstock for the production of electricity and second- generation biofuels e and increasingly now for bio-energy with carbon capture and storage (BECCS) [1,2]. BECCS may lead to negative carbon emissions if the biomass is grown sustainably. Several studies have found that such negative emissions technol- ogies might be essential for achieving stabilization targets of below 450 ppm CO 2 [3,4]. For coal gasication, with and without CCS, the preferred technology is pressurized oxygen-blown entrained ow gasica- tion. The advantages of entrained ow gasication are a high syngas quality with high H 2 and CO concentrations and low tar and hydrocarbon content, as well as a short residence time resulting in compact gasier equipment. Several large-scale coal-fed entrained ow gasiers with a capacity of several hundred MW th are in operation, but none with carbon capture. For biomass, however, pressurized entrained ow gasication is infeasible because of problems related to the feeding system. The gasier requires feedstock at small particle size (0.1 mm for coal). Laboratory-scale tests with pulverized wood indicated that a pneumatic feeding system is not suitable for wood powder, due to the high cohesion between the brous particles [5]. Fluidized bed gasiers accept a particle size of up to 70 mm [6] and are therefore better suited for biomass. Typical plant input capacities range up to 50 MW th [6]. However, the syngas contains tar and CH 4 and is therefore less suited for carbon capture. The foregoing observations indicate three options for biomass gasication with CCS: 1. adopt uidized bed gasication and condition the syngas so that is meets the requirements of the shift reactor and CO 2 removal unit, 2. develop a dedicated biomass feeding system for entrained ow gasiers, 3. pre-treat the biomass to make it suitable for ne milling and use in the conventional pneumatic transport machinery employed in entrained ow gasiers. Research on a dedicated biomass feeding system using screw feeders and piston compressors is presented in Ref. [5]. This system requires particles no smaller than 1 mm, but since biomass * Corresponding author. Tel.: þ49 30 314 28 449; fax: þ49 30 314 21 683. E-mail address: erlach@iet.tu-berlin.de (B. Erlach). Contents lists available at SciVerse ScienceDirect Energy journal homepage: www.elsevier.com/locate/energy 0360-5442/$ e see front matter Ó 2012 Elsevier Ltd. All rights reserved. doi:10.1016/j.energy.2012.01.057 Energy 45 (2012) 329e338