Modelling a biorefinery concept producing carbon fibre-polybutylene succinate composite foam
- Authors: Ghayur, Adeel , Verheyen, Vincent
- Date: 2019
- Type: Text , Journal article
- Relation: Chemical Engineering Science Vol. 209, no. (2019), p. 1-7
- Full Text: false
- Reviewed:
- Description: In this study, a novel biorefinery concept producing carbon fibre-poly(butylene succinate) composite foam (CPC foam) from lignocellulose and CO 2 is modelled. The biodegradable nature of poly(butylene succinate) would allow for easy carbon fibre recovery from the CPC foam for reuse at the end of product lifecycle, thus allowing for a circular materials flow. Technical simulation results show the biorefinery consumes 417 kg of biomass, 33 kg of CO 2 , 86 kg of methanol, 23 kg of acetic anhydride, 130 kWh of electricity and 1166 kW of heat per hour. The facility generates 72 kg of CPC foam, 82 kg of carbon fibre, 24 kg of tetrahydrofuran and 50 kg of dimethyl ether (DME). DME is used to fulfil parasitic electricity requirement. These results demonstrate the technical viability of this biorefinery although, research is needed to reduce parasitic energy demand. This carbon negative biorefinery avoids carcinogens and halogens for polymeric materials synthesis by utilising green chemistry principles and lignocellulose feedstock.
Monoethanolamine degradation during Pilot-Scale post-combustion capture of CO₂ from a brown coal-fired power station
- Authors: Reynolds, Alicia , Verheyen, Vincent , Adeloju, Samuel , Chaffee, Alan , Meuleman, Erik
- Date: 2015
- Type: Text , Journal article
- Relation: Energy & Fuels Vol. 29, no. 11 (2015), p. 7441-7455
- Full Text: false
- Reviewed:
- Description: The use of aqueous amines, such as monoethanolamine (MEA, 2-aminoethanol), for post-combustion capture (PCC) of CO2 from fossil-fuel-fired power station flue gases leads to undesirable reactions with oxygen, SO2, and NO2. This study has used a gas chromatography with mass spectrometry detection (GC-MS) method to measure the changes in concentrations of organic compounds in samples of a 30% (w/w) aqueous MEA absorbent obtained from CSIRO's PCC pilot plant operating at AGL's Loy Yang brown coal-fired power station in Latrobe Valley, Victoria, Australia. This aqueous MEA absorbent was previously used for more than 700 h of PCC, and the collected samples represent a further 834 h of PCC operation. These data provide a new perspective on the close, interdependent relationships between corrosion and amine degradation reactions. Other important outcomes include confirmation that (a) organic degradation products identified during laboratory-scale trials were also produced during pilot-scale PCC and (b) N-(2-hydroxyethyl)imidazole (HEI) is a suitable molecular marker for oxidative degradation of MEA. This investigation has also highlighted areas that require further research, including (a) determination of oxidative degradation mechanisms in both the presence and absence of dissolved transition metals, (b) determination of parameters that limit oxidative degradation during pilot-scale PCC, (c) investigation of the antioxidative or oxygen-scavenging properties of partially oxidized amine absorbents during PCC, and (d) measurement of the concentrations of glycine, glycolic acid, and other potential organic acids during PCC. [ABSTRACT FROM AUTHOR]
- Description: The use of aqueous amines, such as monoethanolamine (MEA, 2-aminoethanol), for post-combustion capture (PCC) of
Structural elucidation of humic acids extracted from Pakistani lignite using spectroscopic and thermal degradative techniques
- Authors: Nasir, Saqib , Sarfaraz, Tahira , Verheyen, Vincent , Chaffee, Alan
- Date: 2011
- Type: Text , Journal article
- Relation: Fuel Processing Technology Vol. 92, no. 5 (2011/05/01/ 2011), p. 983-991
- Full Text: false
- Reviewed:
- Description: The present paper describes the characterization of Pakistan lignite coal, derived humic acids (HAL) and nitrohumic acids (NHA) along with the standard leonardite humic acids (LHA). The study utilized chromatographic and spectroscopic techniques to characterize the structure of coal and derived materials. Pyrolysis coupled to gc/ms was conducted with and without methylating agent (tetramethyl ammonium hydroxide). The pyrolysis study resulted in releasing mainly fatty acid methyl esters, different series of hydrocarbons and α, ω-dicarboxylic acid methyl esters. Triterpenoids, syringic and ρ-coumaric compounds and aromatic compounds derived from lignin moieties were also detected. Fourier transform infrared (FT-IR) and NMR data helped to evaluate the influence of coal rank on regeneration and nitration processes with respect to chemical structural composition of coal and derived materials. FT-IR spectra of four materials were similar except that NHA showed an absorption band at 1532cm−1, thus confirming the presence of -NO2 groups. 13C NMR indicated higher aromaticity and less hydroxylalkyl material in HAL than NHA. The elemental composition and acid functional group content of four materials were also reported. The combination of results from different analytical techniques gives an improved understanding of the Pakistan coal nature and helpful for its future utilization.