共炭化对热缩聚及炭化工艺过程的影响

采用煤沥青闪蒸油为原料,乙烯残油为添加剂,在实验室内进行热缩聚及炭化实验。结果表明:加入添加剂后,缩聚沥青的平均分子结构得到改善,从而显著改善了针状焦的显微组织结构,同时具有良好的脱氮效果。     

Investigation of kinetics of agglomerate growth in oil agglomeration process

In this study, the kinetics of agglomerate growth in a batch oil agglomeration process has been studied using bituminous coal. The effect of operating variables such as kerosene concentration, pulp density and speed of agitation on the agglomeration process was investigated. It has been found that the second-order kinetic equation describes the growth of agglomerates adequately. The growth of the agglomerates in the oil agglomeration process shows a self-preserving growth. Using this, a characteristic curve has been developed. For the prediction of the size distribution of the agglomerates, the d₅₀ values of the agglomerates must be known. Therefore, a model has been developed by using the kinetic equation for estimation of d₅₀ values of agglomerates for this coal. It was shown that the size distribution of the agglomerates for any levels of the process variables studied can be predicted using the equation of characteristic curve and d₅₀ values. Knowledge obtained from this study will be helpful for technological advancement of this kind of study.     

Fate of the chlorine and fluorine in a sub-bituminous coal during pyrolysis and gasification

The fate of the chlorine and fluorine present in a sub-bituminous coal from Indonesia during pyrolysis and gasification has been studied with fixed and entrained bed reactors. The rate profile for HCl evolved in the temperature programmed pyrolysis exhibits the main and shoulder peaks at 480 and 600 °C, respectively. Model experiments and subsequent Cl 2p XPS measurements show that HCl reacts with metal impurities and carbon active sites at 500 °C to be retained as inorganic and organic chlorine forms, from which HCl evolves again at elevated temperatures. It is suggested that the HCl observed in the coal pyrolysis may originate from the above-mentioned chlorine functionalities formed by secondary reactions involving the nascent char. In the CO₂ gasification of the 900 °C char at 1000 °C and 2.5 MPa, any measurable amounts of HCl and HF could not be detected even at a high conversion of 75 wt% (daf), suggesting the accumulation of these halogens in the residual char. When the coal is injected into an O₂-blown, entrained bed gasifier at 1200-1400 °C under 2.6 MPa, the partial oxidation proceeds to a larger extent at a higher O₂/coal ratio, whereas the chlorine and fluorine are enriched in the remaining char, and the extent of the enrichment at the latter stage of gasification is larger with the fluorine. The XPS measurements of the chars reveal the presence of the broad F 1 s peak, which can cover a wide range of binding energies attributable to inorganic and organic fluorine. The halogen enrichment during gasification is discussed in terms of secondary reactions of HCl and HF with char.     

Texaco与Shell煤气化工艺比较分析

煤气化技术对于促进煤炭的综合利用、改善当前资源紧缺状况,并减少环境污染具有重要的意义。阐述了Texaco和Shell煤气化的工艺流程,并对2种煤气化工艺进行了比较分析,找出各自的优缺点,为煤气化工艺的选择提供参考。     

DEVELOPMENT AND VALIDATION OF A PROCESS SIMULATOR FOR DRYING SUBBITUMINOUS COAL

Drying subbituminous coal has never been practiced commercially. The commercial dryers built to date have been designed for drying surface moisture in conjunction with upstream coal preparation facilities. This type of drying is mainly controlled by input energy and the basis of the design is an energy balance. In drying inherent moisture from subbituminous coal, the thermal conductivity of the coal and the diffusion of molecular water within coal particles impose limitations on the process conditions. Energy input and solids residence time in the dryer have to be controlled properly for simultaneously balancing the heat and mass transfer within the coal particles. Improper control of either parameter can cause fires and explosions during the key steps of the drying process—drying and cooling

In parallel to the Anaconda coal drying pilot plant program, a cross-flow, fluid-bed coal drying/cooling process simulator was developed for: (1) understanding the drying phenomena on an individual particle basis; (2) analyzing potential risks and safety limits, and (3) designing the Anaconda pilot plant program

The development of the process simulator was based on both first principles and laboratory data and can be divided into two phases:

1 Development of a semi-mechanistic drying model for Powder River Basin subbituminous coal employing an analytical solution of the diffusion equation

2.Formulation of a fluid-bed cross-bed cross-flow dryer/cooler simulator employing simultaneous heat and mass transfer

This model was validated against process variables data taken on a 4 tph pilot plant. An operable range, or process envelope, has been developed through the pilot plant experience and the process simulation study. Based on the model predictions, an uncertainly range was defined in the design recommendations of a pioneer coal drying plant in scale-up.     

Catalytic coal partial gasification in an atmospheric fluidized bed

The coal partial gasification catalyzed by limestone, sodium carbonate and dolomite was studied using a bench-scale atmospheric fluidized bed in the presence of air and steam at 900 °C. The effects of limestone, sodium carbonate and dolomite on composition, heating value, gas yield of product gas and carbon conversion in the catalytic coal partial gasification have been examined. The experimental results show that the catalysts can effectively improve the gas quality, the heating value and the gas yield of product gas and carbon conversion. The catalytic effect of sodium carbonate is better than that of limestone and dolomite. The increase of limestone loading can enhance the quality of product gas, such as the content of combustible gas, the high heating value and the gas yield, during coal partial gasification. This work was presented at the 6 ^th Korea-China Workshop on Clean Energy Technology held at Busan, Korea, July 4–7, 2006.     

A study of the properties of carbon foam reinforced by clay

A novel carbon foam with high strength and very low thermal conductivity was prepared by thermal treating of coal tar based mesophase pitch mixed with montmorillonite clay. SEM observation showed that less micro-cracking appeared on the cell wall of foam by adding of clay-montmorillonite. Foam mechanical properties were improved and its thermal conductivity was markedly decreased. The compressive strengths were increased by 64%, 96% and 100% when the additive amounts of clay were 2%, 5% and 10% (wt%), respectively. Due to the high thermal insulation and lamellar structure of clay, the thermal conductivity of carbon foam decreases from 2 W/m K to 0.25 W/m K.     

Preparation of zinc ferrite in the presence of carbon material and its application to hot-gas cleaning

In order to develop an efficient absorbent of H₂S in coal gasification, zinc ferrite (ZnFe₂O₄) was prepared in the presence of carbon materials such as activated carbon (AC), activated carbon fiber (ACF), and Yallourn coal (YL). The absorption behavior of absorbents for H₂S was examined using a fixed-bed flow type reactor equipped with a quadrupole mass spectrometer.Carbon material-supported ZnFe₂O₄ exhibited larger desulfurization capacity for H₂S than unsupported ferrites. They could efficiently remove H₂S from 4000 ppm levels in a simulated coal gasification gas to less than 1 ppm at 500 °C. The absorption capacity of H₂S with ZnFe₂O₄/AC, ZnFe₂O₄/ACF, and ZnFe₂O₄/YL exhibited nearly 100% of stoichiometric amount of loaded metal species. They could be regenerated by an air oxidation in O₂-Ar (50 vol%) at 450 °C for 30 min. The regenerated ferrite can be used for repeated absorption of H₂S with a very slight decrease in the absorption capacity.     

Simultaneous reduction of NOx and SO2 emissions from coal combustion by calcium magnesium acetate

The potential of calcium magnesium acetate (CMA) as a medium for the simultaneous control of NO_x and SO_x emissions has been investigated using a pulverized coal combustion rig operating at 80 kW. A US and a UK coal of significantly different sulphur contents were used as primary fuel and CMA was injected in solution form into the combustion gases by horizontally opposed twin-fluid atomisers at temperatures of 1100-1200 °C. SO₂ reductions typically greater than 80 and 70% were found for initial SO₂ levels of 1000 and 1500 ppm, respectively, at Ca/S ratios greater than 2.5. There did not appear to be significant limitation on sulphation by pore blockage using CMA due to the open structure formed during calcination and there is clear potential for zero SO₂ emissions at higher Ca/S ratios. The Ca content of the CMA in the form of CaO, via a droplet drying/particle calcination process, absorbs SO₂ by sulphation processes by penetration into the open pore structure of these particles. The effect of primary zone stoichiometry (λ₁=1.05, 1.15 and 1.4) on NO_x reduction was investigated for a range of CMA feed rates up to a coal equivalent of 24% of the total thermal input. NO_x reductions of 80, 50 and 30% were achieved at a primary zone stoichiometry of λ₁=1.05, 1.15 and 1.4, respectively, for a reburn zone residence time of 0.8 s. At lower equivalent reburn fuel fractions, coal gave greater NO_x reductions than CMA but similar levels were achieved above Rff=18%. The mechanism for NO_x reduction involves the organic fraction of CMA which pyrolyses into hydrocarbon fragments (CH_i), but to a lesser degree than coal, which may then react with NO_x in a manner similar to a conventional ‘reburn’ mechanism where NO_x is partly converted to N₂ depending on the availability of oxygen.     

FORMATION AND FLOW OF GAS BUBBLES IN A PRESSURIZED BUBBLE COLUMN WITH A SINGLE ORIFICE OR NOZZLE GAS DISTRIBUTOR

The characteristics of gas bubbles in a 5 cm diameter bubble column equipped with a single orifice of 1,3 or 5 mm diameter were investigated under system pressure of 0.1-15 MPa. The formation of gas bubbles was strongly affected by the system pressure. Under high pressures a dispersed gas jet was formed at gas velocities where spherical gas bubbles would have been formed at atmospheric pressure. The critical gas velocity between the bubbling regime and the jetting regime was correlated with the liquid phase Weber number and the gas phase Reynolds number based on the gas velocity at the orifice. Bubble size and gas holdup in the main part of the bubble column were also affected by the bubble formation pattern at the distributor