CO₂ gasification of bio-char derived from conventional and microwave pyrolysis

Thermal-chemical processing of biomass is expected to provide renewable and clean energy and fuels in the future. Due to the nature of endothermic reactions, microwave and conventional heating have been applied to this technology. However, more studies need to be carried out to clarify the difference between these two heating technologies. In this work, we investigated two bio-char samples produced from conventional pyrolysis of wood biomass (yield of bio-char: 38.48 and 59.70 wt.%, respectively) and one bio-char produced from microwave pyrolysis with a yield of 45.16 wt.% from the same biomass sample at different process conditions. Various methodologies have been used to characterise the bio-chars. CO₂ gasification of bio-char has also been studied using a thermogravimetric analyser (TGA) and a fixed-bed reaction system. The results show that volatile and carbon contents of the bio-char derived from microwave pyrolysis were between the two conventional bio-chars. However, the microwave bio-char is more reactive for CO₂ gasification, as more CO was released during TGA experiments, and the CO release peak was narrower compared with the CO₂ gasification of the conventional bio-chars. It is suggested that the conventional bio-char is less reactive due to the presence of more secondary chars which are produced from secondary reactions of volatiles during the conventional biomass pyrolysis. While the microwave pyrolysis generates more uniform bio-chars with less secondary char, and therefore, has advantages of producing bio-char for downstream char gasification

Carbonisation of biomass-derived chars and the thermal reduction of a graphene oxide sample studied using Raman spectroscopy

Chars and carbonised chars were produced from three different oxygen-rich precursors (Pinus radiata wood, Phormium tenax leaf fibres, and sucrose crystals). These non-graphitisable carbons were analysed with Raman spectroscopy in order to study the nanostructural development which occurs with increasingly severe heat treatments up to approximately 1000 °C. The thermal reduction of a graphene oxide sample was similarly studied, as this is considered to involve the development of nanometre-scale graphene-like domains within a different oxygen-rich precursor. Increasing the heat treatment temperatures used in the charring and carbonisation processes, led to significant changes in a number of parameters measured in the Raman spectra. Correlations based on these parameter changes could have future applications in evaluating various char samples and estimating the heat treatment temperatures employed during their manufacture. After production heat treatment temperatures exceeded 700 °C, the Raman spectra of the carbonised chars appeared to be largely precursor independent. The spectra of these carbonised chars were similar to the spectra obtained from thermally-reduced graphene oxides, especially when compared to a wide range of other carbonaceous materials analysed using this particular methodology. Partial reduction of a graphene oxide sample due to reasonably mild laser exposures during Raman analysis was also observed

A Study of the Chars Livelihood Programme in Northern Bangladesh

The temporary islands and embankment areas, or chars, of the Jamuna River in northwest Bangladesh are home to three million people: poor and isolated, these rural communities face multiple livelihood challenges. Opportunities to smoothen irregular household cash-flow are limited and households in the region regularly adopt severe coping strategies -- such as the distress sale of assets and reduced food intake -- to meet consumption and emergency needs. The Chars Livelihood Programme (CLP) aims to ensure that most poor char dwellers in the Jamuna River Basin have access to appropriate financial services through Savings Groups

Studying carbonisation with raman spectroscopy

Raman spectroscopy can provide fast and non-destructive analysis of carbonaceous materials. As it is able to detect nanometre-sized structural features, Raman spectroscopy is widely used in the study of carbon nanotubes, fullerenes, graphenes, and many other carbon-rich materials. Raman analysis has previously shown potential for estimating the heat treatment temperatures (HTT) employed in the preparation of Japanese cedar charcoals which suggested future usefulness in quality control . In the current work, Raman spectroscopy was used to investigate the nanostructural development which had occurred within various chars prepared and carbonised at a range of heat treatment temperatures between ≈ 340°C and 1000°C. Chars were produced from sucrose sugar as standard precursor of high purity and two sources of biomass common in New Zealand (Radiata pine wood and Harakeke leaf fibres). In chars produced at lower HTTs, signals could be detected which were interpreted as representing hydrogen-rich amorphous carbon structures. In contrast, the Raman spectra of well-carbonised chars produced at higher HTTs featured signals consistent with graphene-like structures with coherent domains limited in size to below a few nanometres across. Measurement of such signals provides the ability to evaluate the extent of nanostructural development, identify char samples which are ‘undercooked’ when compared to other char samples, and estimate effective HTTs used in the production of a given char sample. More detailed Raman analysis of Radiata-derived chars was carried out, including analysis of chars produced from carbonising pyrolysis tars. Results of Raman analysis were correlated to H/C atom ratios obtained through elemental analysis for these chars produced from Radiata pine

Comparison of coal chars prepared in different devices at similar temperature

The characteristics of chars prepared in both a drop tube furnace (DTF) and a flat flame burner (FFB) at 1300 ºC from seven coals of different rank and maceral composition are the subject of this study. Coal samples sized and sieved to 36-75 μm were fed. The flame temperature of the FFB was achieved with a mixture of methane, air and oxygen whereas two different gas compositions were used in the DTF to account for sub-stoichiometric (2.5% O2) and close to stoichiometric (10% O2) oxygen levels. Determination of micropore surface area was carried out by CO2 adsorption isotherms at 0°C and char reactivity to air was measured at 550 °C in a thermogravimetric analyser (TGA). Overall similar combustion trends were obtained in both devices with burnout decreasing as coal rank increases and CO2 surface areas decreasing up to the medium volatile bituminous coal rank and increasing again for the anthracites. The results reveal a reasonable agreement between burnouts of FFB chars and low oxygen DTF chars whereas higher burnouts were obtained for higher oxygen DTF chars. The CO2 surface areas of the chars reasonably scattered without any systematic trend. The intrinsic reactivities of both series of chars from the DTF were similar to the corresponding FFB chars. Increasing coal rank, intrinsic reactivity of chars from the different combustion conditions decreased.The Principality of Asturias (Principado de Asturias), Project PC04-03 and the Ministry for Education (Ministerio de Educación), Project PSE2-2005Peer reviewe

Analysis of products from the pyrolysis of plastics recovered from the commercial scale recycling of waste electrical and electronic equipment

Three plastic fractions from a commercial waste electrical and electronic equipment (WEEE) processing plant were collected and investigated for the possibility of recycling them by batch pyrolysis. The first plastic was from equipment containing cathode ray tubes (CRTs), the second plastic was from refrigeration equipment, and the third plastic was from mixed WEEE. Initially, the decomposition of each of the plastics was investigated using a TGA linked to a FT-ir spectrometer which showed that the CRT plastic decomposed to form aliphatic and aromatic compounds, the refrigerator plastic decomposed to form aldehydes, CO2, aromatic, and aliphatic compounds, and the mixed WEEE plastic decomposed to form aromatic and aliphatic compounds, CO2, and CO. Each plastic mixture was also pyrolysed in a batch reactor to determine the halogen and metal content of the pyrolysis products, additionally, characterisation of the pyrolysis oils was carried out by GC-MS and the pyrolysis gases by GC-FID and GC-TCD. It was found that the halogen content of the oils was relatively low but the halogen and metal content of the chars was high. The pyrolysis oils were found to contain valuable chemical products and the pyrolysis gases were mainly halogen free, making them suitable as a fuel

Steam gasification of bagasse: Effect of heating rate

Bagasse residue is a potential feedstock for steam gasification, but knowledge of this technology is still small and fragmented. Heating rate is of the most important factors influencing the gasification process. However, this parameter has not yet been fully investigated. In this study, the characteristics of bagasse and its chars were identified, and the effect of heating rate on steam gasification kinetics was studied. Bagasse contained little ash content, comparable to woody biomass, which is beneficial for thermochemical conversion processes. The bagasse char had a high heating value, comparable to coal. Effect of a small change in heating rate from 5 to 15 °Cmin-1 was not observed, while a significant increase from 15 to 1800 °Cmin-1 had a considerable effect on steam gasification kinetics. A char produced at a high heating rate increased gasification kinetics by 1.35 times compared to a char produced at a low heating rate. Results and data produced could be useful for the conception of new gasifiers using bagasse, such as staged-gasifiers in which the char production zone is separated from the gasification zone

The electron donating capacity of biochar is dramatically underestimated

Biochars have gathered considerable interest for agronomic and engineering applications. In addition to their high sorption ability, biochars have been shown to accept or donate considerable amounts of electrons to/from their environment via abiotic or microbial processes. Here, we measured the electron accepting (EAC) and electron donating (EDC) capacities of wood-based biochars pyrolyzed at three different highest treatment temperatures (HTTs: 400, 500, 600 °C) via hydrodynamic electrochemical techniques using a rotating disc electrode. EACs and EDCs varied with HTT in accordance with a previous report with a maximal EAC at 500 °C (0.4 mmol(e−).gchar−1) and a large decrease of EDC with HTT. However, while we monitored similar EAC values than in the preceding study, we show that the EDCs have been underestimated by at least 1 order of magnitude, up to 7 mmol(e−).gchar−1 for a HTT of 400 °C. We attribute this existing underestimation to unnoticed slow kinetics of electron transfer from biochars to the dissolved redox mediators used in the monitoring. The EDC of other soil organic constituents such as humic substances may also have been underestimated. These results imply that the redox properties of biochars may have a much bigger impact on soil biogeochemical processes than previously conjectured