Effect of pressure on the swelling of density separated coal particles

Most of the advanced coal combustion and gasification processes operate under pressurised conditions. Current knowledge of the in situ effect of pressure on coal devolatilisation and swelling, however, is limited, but is essentially required for optimisation of these technologies and to ensure future developments. During heating, fluidity is induced by breaking the coal covalent bonds and forming a plastic state where nucleation occurs, volatiles evolve as bubbles and they flow, diffuse, coalesce and rupture in a complex combination of events that lead to the transient structural evolution of the heated coal particle. The effect of pressure on swelling of individual coal particles is the subject of this work. Density fractions of particles were prepared using a sink-float technique to achieve homogeneous particle properties. Groups of particles from each density fraction were heated in a pressurised single particle reactor at pressures ranging from 0.1 to 5 MPa. The thermal behaviour of each sample was recorded using a long distance microscope attached to a CCD camera. Pressure was found to have parallel and competitive effects on the particle fluidity and transient swelling, resulting in a maximum for both transient and ultimate particle swelling at pressures of 1 MPa. For pressures of over 2 MPa, the observed particle swelling was lower than at higher pressures. In most cases, post-swelling particle contraction was observed with the largest contractions occurring under atmospheric pressure conditions as a result of the major bubble rupture and consequent mass loss. The contraction showed a minimum at 2 MPa and a slight increase at the pressure of 5 MPa thought to be due to an increase of the time the particle remained fluid, enabling the high pressure to further deform the particle. Particles from the lower density group showed larger transient swelling and particle oscillations, while the transient swelling decreased rapidly with increases in the particle density.     

Modelling of combustion characteristics of high ash coal char particles at high pressure: Shrinking reactive core model

Combustion of a single-particle high ash coal char at elevated pressure has been analyzed. A fully transient shrinking reactive core model incorporating a simple mechanistic kinetic scheme is used to study the combustion characteristics of high ash coal char. The model includes heat and mass transfer phenomena, reaction kinetics and intra-particle details. Finite volume method (FVM) has been used to solve partial differential equations representing fully transient conservation equations. The char combustion model predicts the mass-loss profile and burnout time of the char particle at different temperature and oxygen concentration. The computed results are found to agree well with the published experimental findings of pressurized combustion of high ash coal char. The effects of bulk temperature, total pressure and initial particle size on combustion characteristic and burnout time have been examined through model simulation.     

Investigation of an iron-based additive on coal pyrolysis and char oxidation at high heating rates

Iron-based catalysts have been shown to enhance coal pyrolysis and char oxidation at low to moderate temperatures and heating rates (< 1250 K and 1–1000 K/s). Such catalytic activity has not been demonstrated at high heating rates and temperatures approaching pulverized coal combustion applications. The effect of an iron-based additive on coal pyrolysis and char combustion was studied in a flat-flame burner system at high particle heating rates using a Kentucky bituminous coal. Pyrolysis and char reactivity of two treated coals with different catalyst loadings were studied and compared with the untreated coal. The total volatiles yield for the treated coals increased between 14 and 18% (absolute) on a dry ash-free basis compared to the untreated coal in experiments conducted at 1300 K. A first-order char oxidation model was used to compare the apparent char reactivities of the treated and untreated coals measured at 1500 and 1700 K. An increase in apparent char reactivity was observed for both treated samples.     

The physical character of coal char formed during rapid pyrolysis at high pressure

Rapid pyrolysis was conducted in a drop tube reactor using seven coals under various operating conditions. In addition to dense char, porous chars (network char and cenospheric char) were formed by the rapid pyrolysis under certain conditions. Porous char was mainly composed of film-like carbon and skeleton carbon. The pyrolyzed coal char particles were characterized in detail. Morphology and bulk density of porous char were quite different from the dense char formed under the same conditions, but elemental composition and BET surface area were similar to each other. CO₂ gasification reactivity of porous char was lower than dense char in the later gasification stage, and this was ascribed to the low reactivity of skeleton carbon.     

升温速率及水蒸气分压改变对神华煤焦及其显微组分焦气化反应性的影响

用非等温热重法考察了神华煤焦及其显微组分富集物焦的水蒸气气化反应,分析了升温速率、水蒸气分压改变对煤焦及其显微组分富集物焦气化反应性的影响。利用最大反应速率和半衰期两种方法评价了所选样品的气化反应性。结果表明：对神华煤而言,在相同的气化反应条件下,当升温速率和水蒸气分压发生改变时,其气化反应性顺序均为,镜质组富集物焦〉原煤焦〉惰质组富集物焦。     

Effect of pyrolysis pressure and heating rate on radiata pine char structure and apparent gasification reactivity

The knowledge of biomass char gasification kinetics has considerable importance in the design of advanced biomass gasifiers, some of which operate at high pressure. The char gasification kinetics themselves are influenced by char structure. In this study, the effects of pyrolysis pressure and heating rate on the char structure were investigated using scanning electron microscopy (SEM) analysis, digital cinematography, and surface area analysis. Char samples were prepared at pressures between 1 and 20 bar, temperatures ranging from 800 to 1000 °C, and heating rates between 20 and 500 °C/s. Our results indicate that pyrolysis conditions have a notable impact on the biomass char morphology. Pyrolysis pressure, in particular, was found to influence the size and the shape of char particles while high heating rates led to plastic deformation of particles (i.e. melting) resulting in smooth surfaces and large cavities. The global gasification reactivities of char samples were also determined using thermogravimetric analysis (TGA) technique. Char reactivities were found to increase with increasing pyrolysis heating rates and decreasing pyrolysis pressure.     

Gasification behaviour of Australian coals at high temperature and pressure

This paper presents gasification conversion data generated for a suite of Australian coals reacting with oxygen/nitrogen mixtures at 2.0 MPa pressure and at temperatures up to 1773 K, as part of a wider investigation into the gasification behaviour of Australian coals. The effects of O:C ratio, residence time and coal type on conversion levels and product gas composition were investigated under conditions relevant to those present in entrained-flow gasification systems. At higher temperatures, coal conversion levels are, as expected, higher, whilst product gas compositions continue to reflect the relevant gas phase equilibrium conditions. These gas phase equilibrium concentrations show strong dependence on the amount of carbon in the gas phase (i.e. coal conversion). The increased conversion achieved at high temperatures allows the contribution of coal-specific properties such as char structure and reactivity to be investigated in more detail than previously possible. Furthermore, at higher conversion levels the effects of coal type on product gas composition are more apparent than at lower conversion levels. These high temperature, high pressure gasification conversion data have been reconciled with high pressure bench-scale pyrolysis and char reactivity measurements, highlighting the significance of coal-specific effects of key gasification parameters.     

Study of the influence of pressure on enhanced gaseous hydrocarbon yield under high pressure-high temperature coal pyrolysis

The influence of pressure on the yield of gaseous hydrocarbon products derived from pyrolysis of Fushun and Xianfeng coals have been investigated in an anhydrous and confined system. Pyrolysis was performed in sealed gold tubes at 380 °C and under the pressures ranging from 50 to 250 MPa for 24 h. The results show that the effect of pressure on coal pyrolysis and product generation should not be ignored. For the Fushun and Xianfeng lignite, the yields of gaseous hydrocarbon generation increase by 9.1% and 12.7% when the pressure increases from 50 to 250 MPa, respectively. However, the yields of hydrogen gas decrease greatly with pressure. The hydrogen gas yields of Fushun and Xianfeng lignite decrease by 76.5% and 75.9%, respectively, when the pressure increases from 50 to 250 MPa. Yields of carbon dioxide gas of Fushun and Xianfeng coals were enhanced with increasing pressure by 7.4% and 8.9% respectively. Data of stable carbon isotope compositions reveal that the methane and ethane carbon isotope values are also affected by pressure, as they become heavier by approximately 1.2‰ (PDB) when the pressure is increased from 50 to 250 MPa. Simultaneously, the hydrogen isotope compositions of methane and ethane increase by 10.3‰ and 7.1‰, respectively. Our experimental results suggest that the increase in gaseous hydrocarbon yield is resulted from synthesis of carbon dioxide and hydrogen and pressure serves to facilitate the synthetic process.     

The char structure characterization from the coal reflectogram

Coal is a heterogeneous substance and its heterogeneity is identified and characterized by variation in reflectance. The main objective of this paper is to characterize the heterogeneity of char and to correlate it with the coal reflectogram, which accounts for both rank and maceral composition effects. Chars from two density fractions in a set of coals were obtained in a Drop Tube Furnace (DTF) at 1400 °C in N₂ environment. The chars were examined under a Scanning Electron Microscope (SEM) and the morphology information was obtained from the image-processing technique. The average porosity of char changes systematically with the FMR of its parent coals (defined as the summation of each reflectance multiplied with its frequency). The char porosity increased with an increase in FMR up to a critical value around 98. With further increase in FMR, the corresponding char becomes dense. The char macro porosity distribution was found to be related to the coal reflectogram. In general, the char porosity distribution shows two peaks, which corresponds to the inertinite and vitrinite peaks in reflectogram. The intensity depends on the maceral content. The relationship between the char porosity and coal reflectance for this set of sample has been found, which is strongly dependent on the coal rank. However, these findings cannot be applied to coals with a strong maceral association (microlithotype).     

CO2 gasification of Thai coal chars: Kinetics and reactivity studies

Two sized fractions (<75 μm and 150–250 μm) of Ban Pu lignite A and Lampang subbituminous B coals were pyrolyzed in a drop tube fixed bed reactor under nitrogen atmosphere at 500–900 °C. Gasification of coal chars with excess carbon dioxide was then performed at 900–1,100 °C. The result was analyzed in terms of reactivity index, reaction rate and activation energy. It was found that chars at lower pyrolysis temperature had highest carbon conversion, and for chars of the same sized fraction and at the same pyrolysis temperature, reactivity indices increased with gasification temperature. The lower rank Ban Pu lignite A had higher R _s values than higher rank Lampang subbituminous B coals. Smaller chars from both coals had higher R _s values, due to the higher ash content. At present, it can be concluded that, within the gasification temperature range studied, gasification rates of chars obtained at various pyrolysis temperatures showed a linear correlation with temperature. However, additional experiment is needed to verify the correlation.     

Characterization of porous structure of coal char from a single devolatilized coal particle: Coal combustion in a fluidized bed

The combustion characteristics of coal char are highly dependent on initial pore structure of devolatilized char as well as on the structural evolution during the combustion of char. The development of pore structure also throws light on the mechanism of the combustion process. In the present work evolution of pore structure of partially burnt coal char of Indian origin has been investigated experimentally in a batch-fluidized bed and analyzed. The BET surface area, micropore surface area and porosity of char at various levels of carbon burn-off have been determined. Experimental specific surface area has been found to agree well with theoretical prediction using random pore model. Modified random pore model is used to determine the active surface area. Char combustion mechanism based on shrinking unreacted core and shrinking reacted core models are delineated during the course of reaction at various bed temperatures. This is substantiated with the proportional representation of ash and carbon matrix in scanning electron microscope images. It is also concluded that in the present investigation the mean pore size is much smaller and hence the Knudsen diffusion predominates. Analysis based on similar experimental observations and models for pore structure evolution to investigate char combustion reaction regime has not been reported in literature.     

煤焦加压气化反应性研究

利用加压热分析仪,测定了义马煤焦的CO2气化反应性。结果表明:随温度的提高,义马煤焦的反应性和反应速度呈增加趋势,与前期研究常压下的情况一致;压力对气化反应的促进作用不明显,且温度对气化过程的影响大于压力;反应速率在初始阶段最大,随后逐渐减小。经过动力学计算表明:反应速率与温度的关系符合Arrhen ius定律;反应级数随温度增加而减小,近似于线性关系;煤焦活化能大约为60.02 kJ/mol。     

Effects of pressure in coal pyrolysis observed by high pressure TGA

High-pressure thermogravimetric analyzer was employed to investigate the effects of pressure on the thermal decomposition process, which is the very first step in most coal utilizing processes, and pyrolyzates from TGA were analyzed by on-line GC/MS. Results showed that pyrolysis of coal with steam under high-pressure conditions exhibited a slower reaction rate compared to the lower pressure conditions, and the effect is more evident at the high temperature region. Coal rank also exhibited a distinct effect on the pyrolysis rate such that a subbituminous coal showed a bigger effect by steam-addition and pressure than bituminous coals. Weathered coal sample illustrated a slower reaction rate compared to the unoxidized coal. In addition, the implication of pressure effects on pyrolysis has been described.     

Effect of the rate of pulverized coal preheating on char reactivity

The effect of the preheating rate of the char particles from Kuznetsk bituminous coal on their specific reaction rate was determined. The experiments were carried out with char samples with mean diameters of 0.15 and 0.35 mm heated to temperatures of 900–1000°C. It was found that the specific surface area of the initial coal, measured by CO₂ adsorption at 273 K, for rapid and slow heat treatments increased more that two times. According to the results of thermogravimetric analysis, it was established that rapid pyrolysis in a muffle furnace led to the production of char whose maximum specific reaction rate was higher than that of the samples after slow pyrolysis.     

Structural ordering of coal char during heat treatment and its impact on reactivity

The effect of heat treatment on the structure of an Australian semi-anthracite char was studied in detail in the 850-1150°C temperature range using XRD, HRTEM, and electrical resistivity techniques. It was found that the carbon crystallite size in the char does not change significantly during heat treatment in the temperature range studied, for both the raw coal and its ash-free derivative obtained by acid treatment. However, the fraction of the organized carbon in the raw coal chars, determined by XRD, increased with increase of heat treatment time and temperature, while that for the ash-free coal chars remained almost unchanged. This suggests the occurrence of catalytic ordering during heat treatment, supported by the observation that the electrical resistivity of the raw coal chars decreased with heat treatment, while that of the ash-free coal chars did not vary significantly. Further confirmatory evidence was provided by high resolution transmission electron micrographs depicting well-organized carbon layers surrounding iron particles. It is also found that the fraction of organized carbon does not reach unity, but attains an apparent equilibrium value that increases with increase in temperature, providing an apparent heat of ordering of 71.7 kJ mol⁻¹ in the temperature range studied. Good temperature-independent correlation was found between the electrical resistivity and the organized carbon fraction, indicating that electrical resistivity is indeed structure sensitive. Good correlation was also found between the electrical resistivity and the reactivity of coal char. All these results strongly suggest that the thermal deactivation is the result of a crystallite-perfecting process, which is effectively catalyzed by the inorganic matter in the coal char. Based on kinetic interpretation of the data it is concluded that the process is diffusion controlled, most likely involving transport of iron in the inter-crystallite nanospaces in the temperature range studied. The activation energy of this transport process is found to be very low, at about 11.8 kJ mol⁻¹, which is corroborated by model-free correlation of the temporal variation of organized carbon fraction as well as electrical resistivity data using the superposition method, and is suggestive of surface transport of iron.     

Volatilisation and catalytic effects of alkali and alkaline earth metallic species during the pyrolysis and gasification of Victorian brown coal. Part V. Combined effects of Na concentration and char structure on char reactivity

A set of NaCl-loaded Loy Yang brown coal was pyrolysed in a thermogravimetric analyser between 600 and 900 °C. The char sample after pyrolysis was cooled down directly for in situ reactivity measurement with air. The results indicated that the volatilisation of Na during pyrolysis is an important reason for the existence of catalyst loading saturation level with Na as a catalyst in char because the char prepared at high temperature had a limited holding capacity for Na. Under the experimental conditions in this study, the char reactivity showed good linear correlation with the Na concentration in the reacting char. Peak pyrolysis temperature, affecting the release of Cl and distribution of Na in char, is an important factor governing the correlation between the char reactivity and Na concentration in char. The catalytic activity of Na is a result of the interaction between Na and char and thus is greatly dependent on the char/carbon structure. At high char conversion levels where the char structure is more inert and highly condensed, the catalytic activity of Na is reduced compared with its activity at low char conversion levels. The catalytic activity of Na depends on the structure of char.     

Investigation on characteristics of pulverized coal dense-phase pneumatic conveying under high pressure

Experiments of dense-phase pneumatic conveying of pulverized coal were carried out in a test facility with a conveying pressure up to 4 MPa. The influence of fluidization nitrogen flow rate, the flow rate of supplementary nitrogen, and the pressure difference between sending hopper and receiving hopper on the solids to gas ratio and the solid mass flow rate was investigated. Test results indicate that with the increase in fluidization nitrogen flow rate, the solid mass flow rate increases, and the solids to gas ratio increases at first and then declines. When the fluidization of pulverized coal in the sending vessel becomes intensive, with the increase in supplementary nitrogen flow rate, the solids to gas ratio declines and the solid mass flow rate increases. And the solid mass flow rate increases linearly with the increase in pressure difference between two hoppers. The experimental results provide a database for the design and operation of a dense-phase pneumatic conveying system. This work was presented at the 6 ^th Korea-China Workshop on Clean Energy Technology held at Busan, Korea, July 4–7, 2006.     

Effect of pyrolysis temperature on the char micro-structure and reactivity of NO reduction

A phenol-formaldehyde resin (PFR) and a bituminous coal (SH) were pyrolyzed at various temperatures. The structure and the char-NO reactivity were analyzed in order to examine the effect of pyrolysis temperature on the micro-structure of the resulting char and further on the reactivity towards NO. Micro-structure of the char samples was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and Raman spectroscopy. It was indicated that the micro-structure of PFR char and coal char experienced remarkable changes during pyrolysis, which resulted in the decrease of phenolic OH, aromatic hydrogen and more ordered structure. The pyrolysis temperature showed a weak impact on the reactivity of PFR char but comparatively remarkable impact on that of coal char at lower reaction temperature. Mineral matter in coal char presented a weak effect on the reactivity. This paper was presented at the 7 ^th China-Korea Workshop on Clean Energy Technology held at Taiyuan, China, June 26–28, 2008.     

Influence of pressure on the release of inorganic species during high temperature gasification of coal

Alkali metal, sulphur, and chlorine species released during coal gasification are of concern, because they can lead to problems in colder parts of the plant. Therefore, hot gas cleaning technology is recently under development. This clean-up strategy requires a comprehensive knowledge of the release characteristics of inorganic compounds. The principal objective of this work was to provide details of the influence of pressure on the release of key chemical species, e.g. sodium, potassium, sulphur, and chlorine. Hence, a total of 19 different coals were investigated in lab-scale gasification experiments in an electrical heated pressurised furnace at absolute pressures of 2, 4, and 6 bar in an atmosphere of He/7.5v%O₂ at 1325 °C. Hot gas analysis was carried out by molecular beam mass spectrometry. The quantitative results showed a decreasing release of ³⁴H₂S⁺, ³⁶HCl⁺, ³⁹K⁺/³⁹NaO⁺, ⁵⁸NaCl⁺, , and ⁷⁴KCl⁺ with increasing pressure. The discussion was supported by thermodynamic calculations.     

Changes in char reactivity and structure during the gasification of a Victorian brown coal: Comparison between gasification in O2 and CO2

Char reactivity is an important factor influencing the efficiency of a gasification process. As a low-rank fuel, Victorian brown coal with high gasification reactivity is especially suitable for use with gasification-based technologies. In this study, a Victorian brown coal was gasified at 800 °C in a fluidised-bed/fixed-bed reactor. Two different gasifying agents were used, which were 4000 ppm O₂ balanced with argon and pure CO₂. The chars produced at different gasification conversion levels were further analysed with a thermogravimetric analyser (TGA) at 400 °C in air for their reactivities. The structural features of these chars were also characterised with FT-Raman/IR spectroscopy. The contents of alkali and alkaline earth metallic species in these chars were quantified. The reactivities of the chars prepared from the gasification in pure CO₂ at 800 °C were of a much higher magnitude than those obtained for the chars prepared from the gasification in 4000 ppm O₂ also at 800 °C. Even though both atmospheres (i.e. 4000 ppm O₂ and pure CO₂) are oxidising conditions, the results indicate that the reaction mechanisms for the gasification of brown coal char at 800 °C in these two gasifying atmospheres are different. FT-Raman/IR results showed that the char structure has been changed drastically during the gasification process.