Process optimization of a lignocellulosic multi-product biorefinery

2014 - 2015A methodology to reduce the complexity of the process optimization was applied to multiproduct biorefinery fed by lignocellulosic biomass. A process superstructure was built to consider alternative process pathways to levulinic acid, succinic acid and ethanol. A Mixed Integer Non-Linear Problem was obtained and transformed in a Mixed Integer Linear Problem by means of a discretization procedure of the non-linear variables. Rigorous design methods accounting for complete kinetics schemes for hydrolysis and fermentation reactors for the production of levulinic acid, succinic acid and ethanol were included in a biorefinery superstructure optimization. A discretization method was applied to obtain a MILP approximation of the resulting MINLP master problem. The optimal flowsheet of a biorefinery with hardwood feedstock, obtained by maximizing the Net Present Value, yields comparable biomass allocation to levulinic acid and succinic acid (more than 40% each) and the its balance to ethanol. A sensitivity analysis highlighted that the optimal flowsheet and the relevant technical and economic performances are significantly dependent on the economic scenario (chemical products selling price, discount rate) and on the plant scale. Finally, process optimization achieved by maximizing two different economic objective functions, Net Present Value and Internal Rate of Return, provided different optimal flowsheets and biomass allocation to chemical products. The effect of the change of the biomass type and composition on the plant was also considered. Results highlight that the composition of the biomass feedstock in terms of cellulose, hemicellulose and lignin has a significant effect on the biomass allocation to the three product production processes and on the relevant optimal flowsheet. Case studies with a combined use of different seasonal biomass types during the year were also studied to provide a methodology to find the optimal biorefinery flowsheet in real scenarios. In the season based scenario studied, product yield distribution and overall productivity of the plant varies during the different periods provided a constant biomass feed rate. [edited by Author]XIV n.s

Techno-Economic Assessment of Bio-Syngas Production for Methanol Synthesis: A Focus on the Water–Gas Shift and Carbon Capture Sections

The biomass-to-methanol process may play an important role in introducing renewables in the industry chain for chemical and fuel production. Gasification is a thermochemical process to produce syngas from biomass, but additional steps are requested to obtain a syngas composition suitable for methanol synthesis. The aim of this work is to perform a computer-aided process simulation to produce methanol starting from a syngas produced by oxygen–steam biomass gasification, whose details are reported in the literature. Syngas from biomass gasification was compressed to 80 bar, which may be considered an optimal pressure for methanol synthesis. The simulation was mainly focused on the water–gas shift/carbon capture sections requested to obtain a syngas with a (H2 – CO2)/(CO + CO2) molar ratio of about 2, which is optimal for methanol synthesis. Both capital and operating costs were calculated as a function of the CO conversion in the water–gas shift (WGS) step and CO2 absorption level in the carbon capture (CC) unit (by Selexol® process). The obtained results show the optimal CO conversion is 40% with CO2 capture from the syngas equal to 95%. The effect of the WGS conversion level on methanol production cost was also assessed. For the optimal case, a methanol production cost equal to 0.540 €/kg was calculated

Techno-economic assessment of co-gasification of coal-petcoke and biomass in IGCC power plants

A process simulation model of the Integrated Gasification Combined Cycle (IGCC) plant of Elcogas was developed and validated with industrial data. The model was used to assess the technical and economic feasibility of the process co-fired with up to 20% by weight of two local biomass samples (olive husk and grape seed meal). Results indicate promising features of the process in the forthcoming scenario of more severe limitations to CO2 emissions

Modelling and Environmental Aspects of Direct or Indirect Dimethyl Ether Synthesis Using Digestate as Feedstock

The conversion of waste and residues towards high added value products has receiving a growing attention, as a reliable strategy to improve sustainability of emergent processes. Anaerobic digestion converts organic waste into biogas and digestate. While biogas may be used for energetic purpose, digestate has limited uses and with a low profitability. In this paper, dimethyl ether (DME) is adopted as target product which may be produced from digestate-derived syngas. Process simulation is carried out for both direct and indirect synthesis of DME and environmental aspects are assessed

Forecasting Model Validation of Particulate Air Pollution by Low Cost Sensors Data

Environmental pollution in urban areas may be mainly attributed to the rapid industrialization and increased growth of vehicular traffic. As a consequence of air quality deterioration, the health and welfare of human beings are compromised. Air quality monitoring networks usually are used not only to assess the pollutant trend but also in the effective set-up of preventive measures of atmospheric pollution. In this context, monitoring can be a valid action to evaluate different emission control scenarios; however, installing a high space-time resolution monitoring network is still expensive. Merge of observations data from low-cost air quality monitoring networks with forecasting models can contribute to improving significantly emission control scenarios. In this work, a validation algorithm of the forecasting model for the concentration of small particulates (PM10 and PM2.5) is proposed. Results showed a satisfactory agreement between the PM concentration forecast values and the measured data from 3 air quality monitoring stations. Final average RMSE values for all monitoring stations are equal to about 4.5 µg/m3

Techno-economic optimization of a process superstructure for lignin valorization

Lignin, the most abundant aromatic biopolymer on Earth, is often considered a biorefinery by-product, despite its potential to be valorized into high-added-value chemicals and fuels. In this work, an integrated superstructure-based optimization model was set up and optimized using mixed-integer non-linear programming for the conversion of technical lignin to three main biobased products: aromatic monomers, phenol-formaldehyde resins, and aromatic aldehydes/acids. Several alternative conversion pathways were simultaneously compared to assess the profitability of lignins-based processes by predicting the performance of technologies with different TRL. Upon employing key technologies such as hydrothermal liquefaction, dissolution in solvent, or high-temperature electrolysis, the technical lignins could have a market value of 200 €/t when the market price for aromatic monomers, resins, and vanillin is at least 2.0, 0.8, and 15.0 €/kg, respectively. When lower product selling prices were considered, the aromatic monomers and the resins were not profitable as target products

The Transition of Scientific Research from Biomass-to-Energy/Biofuels to Biomass-to-Biochemicals in a Biorefinery Systems Framework

Only through renewable carbon source valorization will it be possible to obtain a high-impact transition from a fossil-based system to a renewable-based system [...

Valorization of OFMSW Digestate-Derived Syngas toward Methanol, Hydrogen, or Electricity: Process Simulation and Carbon Footprint Calculation

This paper explores a possible waste-based economy transition strategy. Digestate from the organic fraction of municipal solid waste (OFMSW) is considered, as well as a low-added value product to be properly valorized. In this regard, air gasification may be used to produce syngas. In this work, the production of methanol, hydrogen, or electricity from digestate-derived syngas was assessed by ChemCAD process simulation software. The process scheme of methanol production comprises the following parts: water gas shift (WGS) with carbon capture and storage units (CCS), methanol synthesis, and methanol purification. In the case of hydrogen production, after WGS-CCS, hydrogen was purified from residual nitrogen by pressure swing absorption (PSA). Finally, for electricity production, the digestate-derived syngas was used as fuel in an internal combustion engine. The main objective of this work is to compare the proposed scenarios in terms of CO2 emission intensity and the effect of CO2 storage. In particular, CCS units were used for methanol or hydrogen production with the aim of obtaining high equilibrium yield toward these products. On the basis of 100 kt/year of digestate, results show that the global CO2 savings were 80, 71, and 69 ktCO2eq/year for electricity, methanol, and hydrogen production, respectively. If carbon storage was considered, savings of about 105 and 99 ktCO2eq/year were achieved with methanol and hydrogen production, respectively. The proposed scenarios may provide an attractive option for transitioning into methanol or hydrogen economy of the future

Techno-Economic Assessment of Bio-Syngas Production for Methanol Synthesis: A Focus on the Water–Gas Shift and Carbon Capture Sections

The biomass-to-methanol process may play an important role in introducing renewables in the industry chain for chemical and fuel production. Gasification is a thermochemical process to produce syngas from biomass, but additional steps are requested to obtain a syngas composition suitable for methanol synthesis. The aim of this work is to perform a computer-aided process simulation to produce methanol starting from a syngas produced by oxygen–steam biomass gasification, whose details are reported in the literature. Syngas from biomass gasification was compressed to 80 bar, which may be considered an optimal pressure for methanol synthesis. The simulation was mainly focused on the water–gas shift/carbon capture sections requested to obtain a syngas with a (H2 – CO2)/(CO + CO2) molar ratio of about 2, which is optimal for methanol synthesis. Both capital and operating costs were calculated as a function of the CO conversion in the water–gas shift (WGS) step and CO2 absorption level in the carbon capture (CC) unit (by Selexol® process). The obtained results show the optimal CO conversion is 40% with CO2 capture from the syngas equal to 95%. The effect of the WGS conversion level on methanol production cost was also assessed. For the optimal case, a methanol production cost equal to 0.540 €/kg was calculated