Synthesis Gas. James G. Speight

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reactions.

      In a gasifier, the feedstock particle is exposed to high temperatures generated from the partial oxidation of the carbon. As the particle is heated, any residual moisture (assuming that the feedstock has been pre-fired) is driven off and further heating of the particle begins to drive off the volatile gases. Discharge of the volatile products will generate a wide spectrum of hydrocarbon derivatives ranging from carbon monoxide and methane to long-chain hydrocarbon derivatives comprising tars, creosote, and high-boiling oil. The complexity of the products will also affect the progress and rate of the reaction when each product is produced by a different chemical process at a different rate. At a temperature above 500oC (930oF) the conversion of the feedstock to char and ash and char is completed. In most of the early gasification processes, this was the desired byproduct but for gas generation the char provides the necessary energy to effect further heating and – typically, the char is contacted with air or oxygen and steam to generate the product gases. Furthermore, with an increase in heating rate, feedstock particles are heated more rapidly and are burned in a higher temperature region, but the increase in heating rate has almost no substantial effect on the mechanism (Irfan, 2009).

      2.5.3 Char Gasification

      The gasification process occurs as the char reacts with gases such as carbon dioxide and steam to produce carbon monoxide and hydrogen. Also, corrosive ash elements such as chloride and potassium may be refined out by the gasification process, allowing the high temperature combustion of the gas from otherwise problematic feedstocks. Although the initial gasification stage is completed in seconds or even less at elevated temperature, the subsequent gasification of the char produced at the initial gasification stage is much slower, requiring minutes or hours to obtain significant conversion under practical conditions and reactor designs for commercial gasifiers are largely dependent on the reactivity of the char, which in turn depends on the nature of feedstock. The reactivity of char also depends upon parameters of the thermal process required to produce the char from the original feedstock. The rate of gasification of the char decreases as the process temperature increases due to the decrease in active surface area of char. Therefore a change of char preparation temperature may change the chemical nature of char, which in turn may change the gasification. The reactivity of char may be influenced by catalytic effect of mineral matter in the char.

      Heat and mass transfer processes in fixed- or moving-bed gasifiers are affected by complex solids flow and chemical reactions. Moving-bed gasifiers are countercurrent flow reactors in which the feedstock enters at the top of the reactor and oxygen (air) enters at the bottom of the reactor. Because of the countercurrent flow arrangement of the reactor, the heat of reaction from the gasification reactions serves to pre-heat the coal before it enters the gasification reaction zone. Consequently, the temperature of the synthesis gas exiting the gasifier is significantly lower than the temperature needed for complete conversion of the feedstock. However, coarsely crushed feedstock may settle while undergoing (i) thermal drying, (ii) pyrolysis-devolatilization, (iii) gasification, and (iv) reduction. In addition, the particles change in diameter, shape, and porosity – non-ideal behavior may result from bridges, gas bubbles, channeling, and a variable void fraction may also change heat and mass transfer characteristics.

      2.5.4 General Chemistry

      Gasification involves the thermal decomposition of feedstock and the reaction of the feedstock carbon and other pyrolysis products with oxygen, water, and fuel gases such as methane. The presence of oxygen, hydrogen, water vapor, carbon oxides, and other compounds in the reaction atmosphere during pyrolysis may either support or inhibit numerous reactions with carbonaceous feedstocks and with the products evolved. The distribution of weight and chemical composition of the products are also influenced by the prevailing conditions (i.e., temperature, heating rate, pressure, and residence time) and, last but by no means least, the nature of the feedstock (Speight, 2014a, 2014b, 2017).

      Chemically, gasification involves the thermal decomposition of the feedstock and the reaction of the feedstock carbon and other pyrolysis products with oxygen, water, and fuel gases such as methane and is represented by a sequence of simple chemical reactions (Table 14.2). However, the gasification process is often considered to involve two distinct chemical stages: (i) devolatilization of the feedstock to produce volatile matter and char, (ii) followed by char gasification, which is complex and specific to the conditions of the reaction – both processes contribute to the complex kinetics of the gasification process (Sundaresan and Amundson, 1978).

      Gasification of a carbonaceous material in an atmosphere of carbon dioxide can be divided into two stages: (i) pyrolysis and (ii) gasification of the pyrolytic char. In the first stage, pyrolysis (removal of moisture content and devolatilization) occurs at a comparatively lower temperature. In the second stage, gasification of the pyrolytic char is achieved by reaction with oxygen/carbon dioxide mixtures at high temperature. In nitrogen and carbon dioxide environments from room temperature to 1000 C (1830 F), the mass loss rate o o of pyrolysis in nitrogen may be significant differently (sometime lower, depending on the feedstock) to mass loss rate in carbon dioxide, which may be due (in part) to the difference in properties of the bulk gases.

      Using coal as an example (Chapter 4), gasification in an atmosphere of oxygen/carbon dioxide environment is almost the same as gasification in an atmosphere of oxygen/nitrogen at the same oxygen concentration but this effect is a little bit delayed at high temperature. This may be due to the lower rate of diffusion of oxygen through carbon dioxide and the higher specific heat capacity of carbon dioxide. However, with an increase in the concentration of oxygen, the mass loss rate of coal also increases and, hence, shortens the burn out time of coal. The optimum value of oxygen/carbon dioxide for the reaction of oxygen with the functional groups that are present in the coal feedstock is on the order of 8% v/v.

      If air is used for combustion, the product gas will have a heat content of ca. 150-300 Btu/ ft3 (depending on process design characteristics) and will contain undesirable constituents such as carbon dioxide, hydrogen sulfide, and nitrogen. The use of pure oxygen, although expensive, results in a product gas having a heat content on the order of 300 to 400 Btu/ft3 with carbon dioxide and hydrogen sulfide as byproducts (both of which can be removed from low or medium heat-content, low-Btu or medium-Btu) gas by any of several available processes (Speight, 2013, 2014a, 2017).

      If a high heat-content (high-Btu) gas (900 to 1000 Btu/ft3) is required, efforts must be made to increase the methane content of the gas. The reactions which generate methane are all exothermic and have negative values, but the reaction rates are relatively slow and catalysts may therefore be necessary to accelerate the reactions to acceptable commercial rates. Indeed, the overall reactivity of the feedstock and char may be subject to catalytic effects. It is also possible that the mineral constituents of the feedstock (such as the mineral matter in coal and biomass) may modify the reactivity by a direct catalytic effect (Davidson, 1983; Baker and Rodriguez, 1990; Mims, 1991; Martinez-Alonso and Tascon, 1991).

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