煤炭行业推行安全生产责任保险作用及问题探讨

为了减少事故及其造成的损失,使企业不致因灾后赔付而陷人困境和摆脱“企业赚钱,政府发丧”的怪圈,在煤炭行业推行安全生产责任保险,把商业保险模式引入安全生产领域,分散转移风险,并运用保险行业风险管理方法,规避、控制和管理风险,强化事故预防,以达到安全发展、可持续发展的目标。笔者在认真研究有关政策法规,搜集整理相关资料,实地凋研考察的基础上,结合我国煤炭行业安全生产以及煤炭行业责任风险管理现状,对我国煤炭行业推行安全生产责任保险的作用以及试点省市安全生产责任保险实施过程中遇到的问题进行了分析探讨。     

煤与瓦斯突出影响因素评价分析的模糊层次分析方法

在综合分析煤与瓦斯突出的影响因素的基础上,采用模糊层次分析法（FAHP）建立了煤与瓦斯突出模糊层次分析模型并进行了实例分析,确定了煤与瓦斯突出各影响因素的权重系数。评价结果表明：地应力、地质构造、瓦斯压力等是影响煤与瓦斯突出的主要因素。为制定相应的煤与瓦斯突出防治措施,提供了科学的理论依据和切合实际情况的评价方法。     

煤矿危险源风险预警与控制的研究

根据现代安全管理的理论与方法,结合煤矿人-机-环境特点和不同煤矿事故的发生机理,对煤矿危险源风险预警和控制的基本理论和方法进行了探讨,提出了基于危险源的煤矿风险预警与控制的一般流程,给出煤矿危险源辨识、风险评价、监控和预警的方法,为煤矿安全管理信息系统提供理论基础。     

Occurrence of benzotriazoles (BTRs) in indoor air from Albany,New York,USA, and its implications for inhalation exposure

Despite the widespread use of benzotriazoles as corrosion inhibitors in many household goods, studies on the occurrence of these compounds in indoor air are scarce. In this study, five benzotriazole derivatives were measured in 83 indoor air samples collected from various locations in Albany, New York, USA. Benzotriazoles were found in a majority of the indoor air samples, and the concentrations of their sum in bulk (vapor plus particulate phases) indoor air ranged from below the method limit of quantification to 492 ng·m^?3 (geometric mean: 5.8 ng·m^?3). The highest geometric mean concentration was found in air samples collected in parking garages (155 ng·m^?3), followed by barbershops (13.6), public places (11.5), auto repair shops (5.2), automobiles (4.5), homes (4.5), offices (3.7), and laboratories (2.8). Inhalation exposure to benzotriazoles was calculated on the basis of the measured geometric mean concentrations and air inhalation rate. The highest exposure dose was found for teenagers, with a geometric mean inhalation exposure dose of 79 ng·day^?1. The body-weight normalized exposure dose, however, was the highest for infants, at 3.2 ng·(kg bw)^?1·day^?1.     

Fingerprinting of Gasoline and Coal Tar NAPL Volatile Hydrocarbons Dissolved in Groundwater

Accidental spills and chronic leaks of fuel oil or other hydrocarbon material (e.g., coal tar) often result in subsurface accumulation of nonaqueous phase liquid (NAPL), which can be a subsequent source of contamination in groundwater. Linking hydrocarbons in groundwater to a source NAPL has been difficult when using standard target analytes (e.g., BTEX) because of differences in partitioning properties of the analytes between the source NAPL and groundwater. Because aqueous solubility is predicted to be the controlling influence in the partitioning of hydrocarbons from NAPL to groundwater, a solubility-based approach to matching dissolved hydrocarbons in groundwater to their source NAPL has been developed and validated for two sites with commonly encountered types of NAPL contamination. Specifically, a gasoline LNAPL and a coal tar DNAPL from two separate sites (West Virginia and California) and groundwater interfaced with these NAPLs were analyzed for approximately 50 gasoline-range hydrocarbons consisting of paraffin, isoparaffin, (mono-) aromatic, naphthene, and olefin compounds (PIANO). Solubility characteristics of selected alkyl aromatic hydrocarbons from the PIANO analysis were used to identify a set of diagnostic hydrocarbons, expressed as hydrocarbon ratios, which were found to be useful in distinguishing the source(s) of hydrocarbons in groundwater. At the West Virginia site, the diagnostic ratios in a downgradient groundwater sample were similar to those of a gasoline NAPL at that site, indicating the source of hydrocarbons to the groundwater was the upgradient gasoline NAPL. The diagnostic ratios of the groundwater in contact with the gasoline NAPL and the remote groundwater were also similar, providing evidence that the diagnostic ratios were retained during transport in the aquifer. At the California site, diagnostic ratios in a cross-gradient groundwater sample differed from those of the coal tar NAPL at that site, indicating that the remote groundwater hydrocarbons did not originate from the coal tar contamination. Environmental factors such as selective degradation of specific isomers and various geological conditions (e.g., soil mineralogy, and organic content) may confound the application of this solubility-based fingerprinting approach. Thus, it is recommended that multiple diagnostic pairs be simultaneously evaluated when considering this fingerprinting approach for specific sites and product types.     

Accurate sampling of PCDD/F in high temperature flue-gas using cooled sampling probes

In a laboratory-scale combustion reactor, flue-gas samples were collected at two temperatures in the post-combustion zone, 700 °C and 400 °C, using two different water-cooled sampling probes. The probes were the cooled probe described in the European Standard method EN-1948:1, referred to as the original probe, and a modified probe that contained a salt/ice mixture to assist the cooling, referred to as the sub-zero probe. To determine the efficiency of the cooling probes, internal temperature measurements were recorded at 5 cm intervals inside the probes. Flue-gas samples were analyzed for polychlorinated dibenzo-p-dioxin and dibenzofurans (PCDD/Fs). Samples collected at 700 °C using the original cooling probe showed higher concentrations of PCDD/Fs compared to samples collected using the sub-zero probe. No significant differences were observed between samples collected at 400 °C. The results indicated that artifact formation of PCDD/Fs readily occurs during flue-gas sampling at high temperatures if the cooling within the probe is insufficient, as found for the original probe at 700 °C. It was also shown that this problem could be alleviated by using probes with an enhanced cooling capacity, such as the sub-zero probe.Although this may not affect samples collected for regulatory purposes in exit gases, it is of great importance for research conducted in the high-temperature region of the post-combustion zone.     

铁及铁铜氧化物对臭氧氧化酸性红B的催化效能

采用自蔓延溶胶凝胶法分别制备了铁氧化物和铁铜复合氧化物催化剂,以酸性红B为降解对象,对比了单独臭氧氧化、铁氧化物和铁铜复合氧化物催化臭氧氧化对酸性红B的降解效果,考察了磁力搅拌速度(500～1 640 r/min)、溶液pH(3～11)、臭氧投加速率(3.55～28.4 mg/min)对铁铜复合氧化物催化性能的影响。结果表明,与单独臭氧氧化比较,铁氧化物和铁铜复合氧化物均能加速酸性红B的降解,促进色度和COD的去除,结合催化剂的表征结果,推断催化剂表面羟基促进臭氧分解产生.OH是其氧化性能较好的主要原因,另外,催化剂的吸附能力对催化性能也有一定影响。随着磁力搅拌速度、溶液pH、臭氧投加速率的增大,铁铜复合氧化物催化臭氧氧化酸性红B的效果越好。     

MnxCe1-xO2／γ-Al2O3催化剂的制备及其催化甲苯的燃烧性能

以γ-Al2O3为载体,以MnxCe1-xO2为催化活性组分,采用浸渍法制备了一系列负载型MnxCe1-xO2／γ-Al2O3催化剂（x=0、0．2、0．4、0．6、0．8、0．9、1）,在固定床反应器中评价了催化剂对甲苯的催化燃烧性能。结果表明,MnxCe1-xO2／γ-Al2O3催化剂的催化活性与催化剂的焙烧温度、活性组分MnxCe1-xO2的负载量以及Mn、Ce摩尔比有显著关系,其中焙烧温度550℃、负载量为20％、Mn、Ce摩尔比为4：1时,即MnxCe1-xO2／γ-Al2O3催化剂对甲苯的催化性能最佳,反应温度为180℃时,甲苯的转化率达到95％。并在连续100h的稳定性操作后,催化剂的活性基本无变化。采用XRD、BET以及SEM等分析测试手段对催化剂的结构以及表面进行了表征。     

某“W”型锅炉炉效低的综合治理

针对某锅炉经济性差的问题,从设备、运行及自动控制等方面分析,并进行了相应整改。影响炉效的主要因素有煤质恶化、灰渣含碳量高、排烟温度高和CO浓度高等,同时炉膛燃烧不稳定也是影响燃烧效率的重要因素。通过漏风整改、制粉系统优化、燃烧优化调整和控制系统优化等方法有效提高了锅炉经济性。研究表明：分析锅炉经济性降低的影响因素时应抓住主要因素,兼顾其他,科学的生产管理是保证锅炉运行经济性的重要基础;入炉煤质恶化是最主要的外在因素;良好的自动控制系统能有效稳定燃烧参数,提高燃烧效率;降低飞灰含碳量的主要工作应集中在制粉系统优化调整;完整而系统的燃烧调整试验能够保证锅炉运行控制参数的科学合理,并需要正确调整氮氧化物排放和锅炉效率之间的关系。     

BiFeO3可见光催化降解甲基紫

采用柠檬酸-硝酸盐燃烧法制备了光催化剂BiFeO₃。采用SEM,XRD,FTIR等技术对光催化剂BiFeO₃进行表征。表征结果显示,光催化剂BiFeO₃晶相纯、粒径小、比表面积大,存在Fe#x02014;O的弯曲振动和伸缩振动。实验结果表明：通过鼓气及加入H₂O₂可有效提高BiFeO₃对甲基紫可见光催化降解的效率;在300mL质量分数为1.5#x000d7;10^-5的甲基紫溶液中加入0.9g光催化剂BiFeO₃和0.1mL质量分数为30%的H₂O₂溶液,当反应时间为240min时,甲基紫去除率可达99%。