基于灰色关联分析法的电缆火灾危险性分析

在分析电缆火灾危险性的基础上,依据电缆燃烧特性试验得到的热释放速率峰值、总热释放量、烟气生成速率峰值、总烟气生成量、火焰传播距离和火增长指数6个参数建立了基于试验的电缆火灾危险性的评价指标体系;运用灰色关联分析法选取每个参数指标的最大值构成参考序列,试验样品P1、P6、P7、T1、T2、D1和D27种电缆的参数数据组成比较序列,得到了表征电缆火灾危险性的关联度;通过关联度大小的比较,进而得出试验所选7种电缆的危险性由大到小的顺序依次为D1P1T1P6D2T2P7;结果表明运用灰色关联分析法评价电缆的火灾危险性是一种科学、有效的方法。     

"负压干法除尘和正压湿法脱硫"工艺在燃煤锅炉烟气治理中的应用

介绍了“负压干法除尘和正压湿法脱硫”工艺在20t／h燃煤锅炉烟气脱硫除尘中的应用,及该工艺的设计过程、实际运行中的问题和达到的效果。     

烧结烟气脱硫灰-矿渣复合粉反应性能的研究

烧结烟气脱硫灰中由于含有大量的亚硫酸钙和游离氧化钙,在将其直接用于胶凝材料时,不但延长凝结时间,降低早期强度,而且还容易导致水泥硬化体体积膨胀,恶化硬化体性能。实验研究了脱硫灰不同掺入方式和掺入量,以及氧化温度对复合粉反应性能的影响。结果表明,在将脱硫灰经过550℃氧化处理后,再采用加水预拌的方式,在脱硫灰掺入量为5%时可获得具有较好反应性能的复合粉。     

燃煤烟气脱汞技术研究进展

中国作为燃煤大国,汞污染非常严重,燃煤汞排放的控制技术将会是一个十分重要的环保课题。了解了一些经典脱汞技术的新进展,同时也关注了一些新兴脱汞技术。通过对比分析,认为可以同时脱除NOx、SOx和Hg的多污染控制控术将会是一个有前途的环保技术。     

双碱法烟气脱硫技术影响因素分析

双碱法在中小型燃煤锅炉的烟气脱硫上有着较广泛的应用,它克服了其他湿法脱硫容易结垢的缺点,且脱硫效率高。主要介绍近几年国内双碱法烟气脱硫效率主要影响因素的理论和实验研究现状,分析了pH值、钠离子浓度、液气比、硫酸根离子的比例和进口二氧化硫浓度等因素对该技术的脱硫效果的影响,提出了该技术目前存在的问题及其今后的发展方向。     

燃煤火电厂石灰石—石膏湿法烟气脱硫系统日常运行环保监督考核方法探讨

从二氧化硫总量减排环保监督管理的实际出发,结合日常监督工作的实例,分析影响烟气脱硫效率的因素,找出脱硫系统容易出现的故障,提出对脱硫系统日常监督考核的重点,探索建立烟气脱硫系统监督考核方法。     

Characterization of organic matter in total suspended particles by thermodesorption and pyrolysis-gas chromatography-mass spectrometry

The organic matter in tropospheric aerosol plays an important role in atmospheric physical and chemical processes. The bulk of organic matter, representing a significant proportion of the total suspended particulate (TSP) mass, is bound to polymeric material whose structure and properties are largely unknown. Here we used thermodesorption gas chromatography/mass spectrometry (Td- GC/MS) to study organic compounds of low molecular mass and pyrolysis gas chromatography/mass spectrometry (Py-GC/MS) to characterize the chemical structure of macromolecules in TSP samples collected in di erent seasons from di erent sites in Guangzhou. n-Alkanes, fatty acids and nitriles were the predominant compounds in the thermodesorption products, whereas aromatics, fatty acids, nitriles and n-alkanes/alkenes were the major compounds in the pyrolysates. The results indicated that aromatics were main units in macromolecules. The fatty acids and nitriles formed from carboxylic ammonium salts were detected in both thermodesorption products and pyrolysates at a certain concentration, indicating the importance of these compounds in TSP formation. The TSP source mainly determined the occurrence of compounds in samples from urban, suburban and forest sites, whereas the TSP source and formation process maybe controlled the seasonal variation in compounds detected. High levels of nitriles in summer samples from suburban and forest sites coincide with the release of ammonium from the land and of fatty acids from vegetation at these sites.     

燃煤锅炉烟气氨法脱硫技术的应用

电厂燃煤锅炉烟气脱硫是减少和控制酸雨的有效手段。LS氨法喷雾脱硫技术具有脱硫效率高、环境效益好、资源综合利用的特点。以合成氨生产装置回收的低浓度氨水为吸收剂,实施锅炉烟气脱硫技术改造．取得良好的应用效果。     

Evaluation of mercury speciation and removal through air pollution control devices of a 190 MW boiler

Air pollution control devices (APCDs) are installed at coal-fired power plants for air pollutant regulation. Selective catalytic reduction (SCR) and wet flue gas desulfurization (FGD) systems have the co-benefits of air pollutant and mercury removal. Configuration and operational conditions of APCDs and mercury speciation a ect mercury removal e ciently at coal-fired utilities. The Ontario Hydro Method (OHM) recommended by the U.S. Environmental Protection Agency (EPA) was used to determine mercury speciation simultaneously at five sampling locations through SCR-ESP-FGD at a 190 MW unit. Chlorine in coal had been suggested as a factor a ecting the mercury speciation in flue gas; and low-chlorine coal was purported to produce less oxidized mercury (Hg2+) and more elemental mercury (Hg0) at the SCR inlet compared to higher chlorine coal. SCR could oxidize elemental mercury into oxidized mercury when SCR was in service, and oxidation e ciency reached 71.0%. Therefore, oxidized mercury removal e ciency was enhanced through a wet FGD system. In the non-ozone season, about 89.5%–96.8% of oxidized mercury was controlled, but only 54.9%–68.8% of the total mercury was captured through wet FGD. Oxidized mercury removal e ciency was 95.9%–98.0%, and there was a big di erence in the total mercury removal e ciencies from 78.0% to 90.2% in the ozone season. Mercury mass balance was evaluated to validate reliability of OHM testing data, and the ratio of mercury input in the coal to mercury output at the stack was from 0.84 to 1.08.     

纳米催化剂Pd/SnO_2的制备及催化还原硝酸盐反应的调控

采用热分解法制备了SnO2载体,并用浸渍法制备了Pd/SnO2催化剂.同时,采用X射线衍射仪(XRD)、透射电镜(TEM)、扫描电镜(SEM)及BET比表面积仪等对所制载体和催化剂材料进行了分析表征.结果表明,热分解法和浸渍法都能够获得纳米材料,SnO2及Pd/SnO2的粒径均在9～10nm左右,比表面积分别达到144.99m·2g-1和147.36m·2g-1.在以甲酸为还原剂的Pd/SnO2催化还原硝酸盐体系中,在Pd与SnO2负载比为2%～7%,反应温度为20～50℃和甲酸投加量4.0～24.0mmol·L-1的条件下,催化活性为0.70～9.48mg·min-·1g-1,且催化活性随着负载比、温度和甲酸投加量的增大而增大,随着pH的升高先升后降,最佳pH为3.反应温度升高及pH降低都能够提高Pd/SnO2的选择性.甲酸-Pd/SnO2催化还原硝酸盐体系中还原反应的调控策略为:反应温度宜控制在40～50℃内,这样可同时获得较高的催化活性和选择性,温度过高对催化活性和选择性影响很小,温度过低则会同时降低催化活性和选择性;控制pH为3时,可以获得最大的催化活性及较好的选择性,pH升高会降低Pd/SnO2的催化活性和选择性,pH降低会导致催化活性迅速降低,但对选择性影响不大;甲酸与硝酸盐的物质的量比宜大于4:1,此时可以有效地抑制pH的上升,同时获得较高的催化活性和选择性,甲酸与硝酸盐的物质的量比小于4:1时,会同时降低Pd/SnO2的催化活性和选择性.