缓慢炭化部分氧化对制备煤质活性炭的影响

研究了炭化升温速度、炭化低温区引入空气部分氧化对活性炭制备过程中炭化阶段、炭化物结构、活性炭性能等的影响。结果表明，炭化时低温部分氧化可提高炭化物得率，使炭化物微晶的ｄ００２值升高和Ｌｃ值减小；而较慢的炭化升温速度有利于制备优质活性炭。缓慢炭化、部分氧化可以在一定程度上控制炭化路径，使炭化向生成取向性差、难石墨化、各向同性、呒定形炭多的炭化物的方向进行；并讨论了它们控制炭化的作用机理。以此为指导，     

氧弹分解-原子荧光法测定煤中汞的研究进展

介绍氧弹分解-原子荧光法测定煤中汞含量的研究进展。影响该方法主要因素为称样量、氧气浓度、吸收剂、还原剂、煤种以及灰分含量。分别综述了各个因素对该方法的影响,可为相关标准的制定提供参考。该方法能够简单、经济、快速地测定煤中汞的含量,但是目前学者们对于该方法的相关研究还存在分歧,需要进一步的研究验证;同时,还需要注意以下几个研究方向:吸收剂和还原剂的选择对汞回收率的影响;吸收剂在密闭氧弹中对汞的回收率及吸收时间的研究;氧弹废气中汞含量的测定;煤种和灰分含量对汞含量测定的影响。     

The utility of Bacillus subtilis as a bioflocculant for fine coal

The application of Bacillus subtilis as a flocculant for fine coal has been reported here. Zeta-potential measurements showed that both the coal and bacteria had similar surface charge as a function of pH. Surface free energy calculations showed that the coal was hydrophobic while the bacterium was hydrophilic. The adhesion of the bacteria to coal and subsequent settling was studied in detail. Adhesion of bacteria to coal surface and subsequent settling of coal was found to be quick. Both adhesion and settling were found to be independent of pH, which makes the process very attractive for field applications. The presence of an electrolyte along with the bacterium was found to not only enhance adhesion of bacteria, but also produce a clear supernatant. Further, the settled fraction was more compact than with bacteria alone. Interaction energy calculations using the extended DLVO theory showed that the electrical forces along with the acid–base interaction energy play a dominant role in the lower pH range. Above pH 7, the acid–base interaction energy is the predominant attractive force and is sufficient enough to overcome the repulsive forces due to electrical charges to bring about adhesion and thus settling of fine coal. With increase in electrolyte concentration, the change in total interaction energy with pH is minimal which probably leads to better adhesion and hence settling.     

Groups of paramagnetic centres in coal samples with different carbon contents

Complex systems of paramagnetic centres existing in demineralised flame coal (71.4 wt% C), medium-rank coal (85.6 wt% C) and anthracite (94.9 wt% C) were analysed by electron paramagnetic resonance spectroscopy (EPR). Different groups of paramagnetic centres were searched in macerals (exinite, vitrinite, inertinite) of coals with carbon contents of 73.8 wt% C and 85.6 wt% C. Experimental EPR spectra were fitted by different superposition of theoretical lines. Total concentration of paramagnetic centres both in coal and macerals increases with carbon content in the sample. Total concentration of paramagnetic centres in macerals increases from exinite to inertinite. Four groups of paramagnetic centres were found in medium-rank coal, and only two groups exist in flame coal and anthracite. The EPR spectrum of medium-rank coal is a superposition of two broad and two narrow lines. Both broad and narrow, and two narrow lines were measured in EPR spectra of flame coal and anthracite, respectively. Two types of paramagnetic centres with broad lines and one group with narrow lines exist in exinite and vitrinite from medium-rank coal. Two narrow components were observed in EPR spectra of its inertinite. Two different broad electron paramagnetic resonance signals were detected for macerals from low-coalificated coal. Paramagnetic centres systems of medium-rank coal samples reveal the most complex character. Broad EPR lines were not observed for the higher coalificated samples, i.e., anthracite and inertinite from medium-rank coal. Narrow lines do not occur in EPR spectra of low-coalificated macerals. Strong dipolar interactions and fast spin-lattice relaxation processes are characteristic for paramagnetic centres with broad lines. Strong exchange interactions and short spin-lattice relaxation time were measured for paramagnetic centres with the narrowest EPR signals.     

Pyrolysis and TG Analysis of Shivee Ovoo Coal from Mongolia

The coal sample of the Shivee Ovoo deposits has been non-isothermally pyrolysed in a thermogravimetric analyser to determine the influence of temperature, heating rate and purge gas employed on the thermal degradation of the sample. The heating rates investigated in the TG were 10–50 K min^–1 to final temperature of 1000°C. N₂or CO₂ were employed as well as type of purge gas on the process of thermal degradation of the coal sample. The coal was also investigated in a fixed bed reactor to determine the influence of temperature and heating rate of the pyrolysis on the yield of products and composition of the gases evolved. The main gases produced were H₂, CH₄, C₂H₂, C₂H₄, C₂H₆, C₃H₆ and C₃H₈ and also minor concentrations of other gases. This revised version was published online in August 2006 with corrections to the Cover Date.     

水煤浆添加剂与煤之间的相互作用规律研究 Ⅰ. 复合煤颗粒间的相互作用对水煤浆流变性的影响

使用12种不同分散剂对14种不同变质程度的煤进行了成浆性实验，分析了182个水煤浆(CWS)样品的流变性。结果表明，低变质程度和高灰煤浆多呈屈服假塑性，煤的性质起主导作用；变质程度高且灰分较低煤浆的流变性，主要依赖于分散剂的结构与性质；分子结构单元立体空间效应大，疏水基团与亲水基团呈立体间隔分布的分散剂，易形成屈服假塑性CWS；分子线度长，亲水基团与疏水基团呈线性间隔分布的分散剂，易形成胀塑性CWS。复合煤粒间的相互作用方式是决定CWS流变特性的关键。     

粉煤灰与几种酸固相反应特性的表面分析

用扫描电镜．能量色散谱研究了粉煤灰与酸的固相反应过程中表面形貌和化学组成变化特性。室温下粉煤灰分别与HCI、HNO3、H2SO4、HCIO4固相反应后，表面产生直径20—200nm的结晶颗粒或晶柱。反应生成的水溶物结晶体的扫描电镜图像分别呈手指状、龟背形、蛛蛛状、蝙蝠态，分别为氯化铝铁混晶、硝酸铝铁混晶、硫酸铝铁混晶和高氯酸铝铁混晶。粉煤灰是硅、铝、铁等元素的氧化物聚集体，铁铝等氧化物主要分布在颗粒表面，氧化硅主要分布在颗粒内层。用少量酸进行固相反应这些氧化物聚集体可相互剥离，用H2SO4处理粉煤灰优先将铁铝氧化物转化成可溶性硫酸盐。     

煤炭码头船货匹配下泊位动态分配多目标优化模型及算法

本文针对输出型煤炭码头船货匹配下泊位动态分配问题,构建了堆场-取装线-泊位-船舶联合分配优化数学模型,并设计了采用仿真推演策略解码的遗传算法求解。首先,综合考虑船舶、泊位、堆场、取装线、煤种、航道开放时间和装船作业规则等要素,以船舶在港时间最短和作业效率最大为目标建立了相应的多约束多目标优化模型。然后,综合多目标优化、遗传算法以及仿真推演技术,设计了相应的遗传算法求解,包括:组合式编码、采用仿真推演策略的解码方法,追加了具有合法性检查的染色体生成算法,设计了采用多种策略的遗传操作等。最后实例表明,本算法的执行效率高而且优化效果好。     

用超临界气体抽提方法研究抚顺烟煤的组成和结构——Ⅰ.抽出物的分离及GC、GC/MS分析

将抚顺烟煤用甲苯作溶剂,在半连续抽提装置上,于350℃、20MPa条件下,进行超临界气体抽提。抽出物先分离成油、沥青烯及前沥青烯三个族组份,再用离子交换树脂、硅胶柱色谱作进一步分离。GC和GC/MS的分析结果表明,油段分中存在正构烷烃(C_(13)—C_(31))、类异戊二烯化合物及长链烷基苯系列,这些化合物可提供抚顺烟煤的地球化学信息。     

Electron microprobe analysis of micro amount powder samples: A case study on high purity coal

For the major, minor and trace element analysis of the inorganic compounds of a Ruhr-Saar coal different preparation techniques are investigated with X-ray fluorescence analysis, electron microprobe and classical wet chemical methods minimizing sample weight at standard preparation times and analytical accuracies. Considering accuracy as well as preparation efforts, determinations by electron microprobe on small sample amounts (<50 mg) proved to be superior to the other methods.Abbreviations AAS atomic absorbtion spectrometry - EMA electron microprobe analysis - IC ion chromatography - ISE ion sensitive electrode - PHOT photometry - WCA wet chemical analysis - XRF X-ray fluorescence analysis - LTA low temperature plasma ashing - HTA high temperature ashing - l.o.i. loss on ignition