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91.
A suite of density-differentiated macerals from several coals was analysed by Fourier transform infrared spectroscopy to obtain information on the nature and magnitude of the variations exhibited by the various maceral fractions. The most characteristic change between maceral groups was the variation in aliphatic hydrogen content, with exinite ? vitrinite ? inertinite. Since the separation technique (density gradient centrifugation) generally provided a number of fractions within a maceral group region, some of these were also analysed. In a series of density fractions from a low rank vitrinite, it was found that the aliphatic hydrogen content decreased as the density increased. The inertinites also exhibited a decrease in aliphatic hydrogen. The inertinite C—O bands had extinction coefficients different from those of vitrinites or exinites. The data suggest that quite profound variations in organic structure as determined by FT-i.r. spectroscopy can exist within a maceral group, so that for the most critical work on coals it is necessary to take this into account.  相似文献   
92.
Y.F. Chiu  M.T. Hong 《Fuel》1983,62(10):1150-1152
The relations between coke yields and the volatile matter content of 30 individual and 30 blended coals were investigated. Coke yields and deposited carbon related to volatile matter content can be expressed in the following equations: CY (%) = 97.89?0.86 VMch+VMc; and DC (%)= ?2.24+0.16 VMch; where: CY=real coke yield; VMch = volatile matter content of charging coal; VMc=volatile matter content of coke, and in the case of <2%; DC = deposited carbon. The test results show excellent correlation with practice.  相似文献   
93.
Using low-rank coals, the modifying activities of some petroleum, coal tar and aromatic hydrocarbon additives have been examined to find procedures for their utilization in the preparation of blast furnace coke. Petroleum pitch, especially after hydrogenation, exhibited excellent modifying activity even with non-fusible coals. In contrast, the activity of coal tar was very limited with such coals. The napththenic component, revealed by n.m.r. of the additives, appears to be important in the co-carbonization by inducing fusibility and anisotropic development in such coals. Co-carbonization to recover the dehydrogenated additives was attempted. However, there was no development of the anisotropy in the resultant coke by dissolution of the coal particles although the coal particles were firmly fixed in the matrix. Acid-refluxing treatment of non-fusible coals was found to enhance their modification susceptibility, indicating that some of the acid-soluble mineral matter is important in the thermal depolymerization or fusion process of the coal.  相似文献   
94.
57Fe Mössbauer spectroscopy has been used to characterize the iron-bearing minerals present in some British Columbia coals. The minerals observed in a range of samples include pyrite/marcasite, siderite, jarosite, rozenite or melanterite, and Fe2+ -bearing clay minerals such as illite. The presence of jarosite is confirmed through the magnetic hyperfine interaction observed at 4.2 K. The absence of magnetic ordering at 4.2 K for the ferrous sulphate component indicates the presence of rozenite, FeS04 · 4H20, or melanterite, FeS04 · 7H20, rather than szomolnokite, FeS04 · H20 or FeS04. The effects of ashing on two of the coals is also studied.  相似文献   
95.
Bituminous coal samples from 84 distinct sources were analysed by conventional British Standards (BS) methods for phosphorus, sulphur, chlorine, ash and the ash-forming elements (calcium, silicon, aluminium, iron, sodium, magnesium, potassium, titanium and manganese). In most cases four determinations were made per element per source. Samples were crushed to ?212 μm (72 BS mesh) and pressed into aluminium cups at 20 t in?2 (309 MPa) without binder or backing. Two pellets from each sample were analysed by wave-length dispersive X-ray fluorescence techniques, using a spectrometer equipped with a rhodium rube; the X-ray count took 60 s. The X-ray results were calibrated against the conventional results using multiple regression. The accuracy obtained was comparable with routine ‘wet chemical’ techniques. The X-ray technique is suitable for the routine determination of large numbers of samples.  相似文献   
96.
根据国家质量技术监督局的计划安排,国家标准GB/T15224-1994《煤炭质量分级》需要修订。本文主要讨论“煤炭硫分分级”方面的内容。  相似文献   
97.
在线煤灰分检测技术在中国的应用   总被引:1,自引:0,他引:1  
介绍了应用双能量γ射线透射法测量煤灰分的技术原理及特点;清华大学工程物理系采用该法研制的在线煤灰分仪应用在选煤厂可以指导生产,保证产品质量,提高选煤效率,还可用于介耗<2kg/t的重介质选煤厂及自动配煤系统,为企业创造了显著的经济效益。  相似文献   
98.
铂丝还原滴定法在测量干法脱硫后硫化物含量时,测量数据偏离实际结果,容易造成触媒中毒。提出了用气相色谱火焰光度检测器测定的方法,使数据更可靠、准确。  相似文献   
99.
Claus F.K. Diessel 《Fuel》1983,62(8):883-892
Widespread disagreement about the degree of reactivity of the inertinite group of macerais is related to variations in experimental conditions of assessment and failure to appreciate technological modifications imposed on similar macerals by dissimilar source materials and depositional conditions. This has resulted in the constant under-estimation of the coking potential of post-Carboniferous inertinite-rich coals by predictive methods developed for vitrinite-rich Carboniferous coals. Coking tests up to 1000 °C have been carried out on 20 coals of different rank in such a manner that coked portions of the samples could be correlated with their uncoked equivalents. It has been found that an inverse relationship exists between the level of precarbonization reflectance (PCR) of inertinite and the reflectance and bireflectance of its coke. The increase in the latter parameter is non-linear and involves a sudden jump which is taken as the boundary between reactive (high bireflectance) and non-reactive (low bireflectance) inertinite. In relation to coal rank a reactivity field for inertinite has been delineated which can be subdivided into two areas of high and moderate reactivity, respectively. On the whole, the proportion of reactive inertinite is larger than allowed for in most petrography-based coke stability calculations.  相似文献   
100.
吴迎 《化工设计通讯》2006,32(2):1-2,10
介绍气化效率高、有利于环保、具有一定竞争力的Shell煤气化工艺原理、技术特点及关键设备。建议尽快实现关键技术和设备的国产化。  相似文献   
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