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61.
The bio-briquette technique which mixes coal, biomass and sulfur fixation agent and bio-briquettes under 3-5 t/cm^2 line pressure has aroused people‘s attention in view of controlling the air pollution and the acid rain. In this paper, the physicochemical properties of bio-briquette and its ash were investigated. And the acid soil was improved by the bio-briquette combustion ash, which contained nutritive substances such as P, N, K and had the acid-neutralizing capacity(ANC). The pH, EC, effective nutrient elements(Ca, Mg, K, P and N), heavy metal elements(AI, Cu, Cd, Cr, Zn and Mn) and acid-neutralizing capacity change of ash-added soils within the range of 0-10%, were also studied. Specially, when 5% bio-briquette combustion ash was added to the tested soil, the content of the effective elements such as Ca, Mg and K rose by 100 times, ? times and twice, respectively. The total nitrogen also increased by about twice. The results showed the oxyanions such as that of AI, Cu, Cd, Cr, Zn and Mn were not potentially dangerous, because they were about the same as the averages of them in Chinese soil. It is shown that the ANC became stronger, though the ANC hardly increases in the ash-added soil. On the basis of the evaluation indices, it is concluded that the best mixture ratio is to add 2.5%--8% of the bio-briquette combustion ash to the tested soil. 相似文献
62.
实验室研制了低能光电子磁场增强电离(MEPEI)和单光子电离(SPI)复合电离源,该电离源具有电离化合物范围宽、碎片离子少、质谱图简单等优点,结合飞行时间质谱(TOF-MS)实现了聚氯乙烯(PVC)热分解/燃烧产物的在线分析.针对不同的目标化合物,MEPEI/SPI复合电离源通过调节电离区电场强度,可以快速在SPI和SPI-MEPEI之间切换.PVC热分解/燃烧产物中电离能大于光子能量(10.60 eV)的HCl和CO2(12.74 eV、13.77 eV)利用MEPEI模式电离;而烯烃、二氯乙烯、苯系物、氯苯、苯乙烯、茚满及萘系物等可通过SPI-MEPEI复合模式电离.通过实时监测PVC主要燃烧产物的信号强度随温度的变化趋势可推断出,PVC燃烧产物主要是通过两种机制生成:①250～370℃时,PVC发生脱氯及分子内环化反应,产生大量的HCl、苯和萘;②380～510℃时,PVC发生分子间交联反应,生成烷基芳烃,如甲苯和二甲苯/乙苯等.实验结果表明,SPI/SPI-MEPEI复合离子源TOF-MS分析速度快,应用范围广,在在线分析中具有广泛的应用前景. 相似文献
63.
Ashleigh Cousins Sanger Huang Aaron Cottrell Paul H.M. Feron Eric Chen Gary T. Rochelle 《Greenhouse Gases: Science and Technology》2015,5(1):7-16
Concentrated piperazine (PZ) is a promising new solvent under consideration for post‐combustion capture (PCC) of CO2. A solution of 8 molal PZ was recently evaluated at the Tarong CO2 capture pilot plant in Australia. Initial operation involved evaluation of different operating conditions at the plant to determine the minimum energy conditions for this solvent. Comparison was made to results achieved previously at the same pilot plant with 30 wt% monoethanolamine (MEA). Regeneration energy requirements achieved with concentrated PZ were consistently lower than those achieved with MEA. The lowest regeneration energy for PZ at the pilot plant (2.9 MJ/kgCO2) was roughly 15% lower than the best result predicted for MEA. Inter‐cooling located at the center of the absorber column was also evaluated for the concentrated PZ solvent. The benefit of inter‐cooling was found to depend on the operating conditions of the plant, with operation at higher liquid‐to‐gas (L/G) ratios showing a more pronounced effect. For an L/G ratio of 3.3 kg/kg, inter‐cooling was found to lower the regeneration energy required for PZ by approximately 10%. 相似文献
64.
为研究民用固体燃料燃烧的大气污染物排放特征,设计了一套箱式稀释采样测试系统.相比于常用的烟罩法和烟道采样法,该系统能减小环境空气中颗粒物对测试结果的影响,同时收集了炉具泄漏的烟气,能更准确获得固体燃料燃烧的大气污染物排放水平.本文介绍了该系统的设计思路、主要结构组成和测试系统的性能评估结果.评估结果表明：进气经过滤后颗粒物浓度显著下降至约1 μg·m-3,远小于燃烧过程中排放的颗粒物浓度（约100 μg·m-3）,有效减少环境空气中颗粒物对测试结果的干扰;使用箱式法测得PM2.5、SO2和NOx排放因子结果均高于箱体敞开的对照组测试,证明箱式法收集测试了燃烧时泄漏至室内的污染物,有效减少污染物泄漏造成的误差.利用该系统测试了12种常见民用煤和3种生物质燃料燃烧 PM2.5、SO2、NOx等污染物排放水平,其中民用煤PM2.5、SO2和NOx排放因子分别为0.23～3.40 mg·g-1、0.48～6.15 mg·g-1和0.16～1.09 mg·g-1,生物质燃料的PM2.5、SO2和NOx排放因子分别为6.26～39.76 mg·g-1、0.04～0.23 mg·g-1和0.05～0.76 mg·g-1. 相似文献
65.
为改善湖泊沉积物-水界面生境,开发了一种可原位供氧同时削减内源氮释放的缓释氧材料。发现以m（CaO2）：m（白土）：m（水泥）=2：1：1制备的缓释氧材料具有较好的释氧和pH缓冲能力。通过模拟实验比较缓释氧材料不同投加方式（表层投加和泥内投加）对释氧和沉积物中污染物释放的影响。结果表明：1）表层投加缓释氧材料使得上覆水中DO浓度和pH值明显升高,而在泥内投加可以使pH值维持在7.5以内,同时DO浓度缓慢增加,延长了释氧周期;2）缓释氧材料对沉积物中NH4+-N释放有显著的抑制作用,且表层投加方式明显高于泥内投加,以空白组作参比,静态培养31 d后,泥内加入缓释氧材料对NH4+-N的抑制率为53.4%,而表层投加对NH4+-N的抑制率达到81.1%,投加释氧材料有利于提高上覆水DO水平,促进硝化细菌的生长,从而抑制NH4+-N的释放;3）缓释氧材料有利于微生物生长,促进了微生物腐殖化作用,从而对沉积物中类陆源腐植酸的释放略有促进,而对类酪氨酸蛋白释放略有抑制;4）缓释氧材料可促进沉积物中Fe/Al-P向Ca-P转化,对DIP的释放略有抑制,但由于pH增加导致沉积物中DOC以及重金属As和Cr的释放略有增加。 相似文献
66.
催化燃烧法处理炼油污水处理场臭气 总被引：1，自引：0，他引：1
申屠灵女 《石油化工环境保护》2003,26(4):36-39
介绍了污水处理场臭气来源、危害和影响，从技术、经济和环境效益等方面对几种处理方法进行了比较，提出了采用催化燃烧法的技术实施方案。 相似文献
67.
68.
Xiao Chen Yong Wang Jianyu Li Zhongheng Hu Ying Zhou Huayan Liu Hanfeng Lu 《环境科学学报(英文版)》2022,34(6):114-124
The preparation of highly active supported noble metal catalysts with a low noble metal loading has always been the ultimate goal of researchers working on catalysis. Hydrothermally treated Pt/Al2O3 (Pt/Al2O3-H) exhibits better catalytic activity than that (Pt/Al2O3-C) treated via the conventional calcination approach. At the high space velocity of 100,000 mL/(g∙hr), the temperature that correspond to 50% toluene conversion (T50) of Pt/Al2O3-H is 115°C lower than that of Pt/Al2O3-C, and the turnover frequency (TOF) value can reach 0.0756 sec−1. The mechanism by which the hydrothermal approach enhances Pt/Al2O3 activity has been investigated. The structure associated with the high catalytic activity of Pt nanoparticles (NPs) can be retained via hydrothermal treatment. Furthermore, the support is transformed to AlO(OH) with numerous surface hydroxyl groups, which in turn can facilitate the adsorption of toluene. And the synergistic effects of Pt NPs and AlO(OH) increases the contents of Pt in oxidation state and active oxygen, which are beneficial for toluene oxidation. 相似文献
69.
Christof Lanzerstorfer 《环境科学学报(英文版)》2017,29(4):178-183
Miscanthus giganteus is one of the energy crops considered to show potential for a substantial contribution to sustainable energy production. In the literature there is little data available about the chemical composition of ashes from the combustion of Miscanthus and practically no data about their physical properties. However, for handling, treatment and utilization of the ashes this information is important. In this study ashes from two biomass combustion plants using Miscanthus as fuel were investigated. The density of the ashes was 2230 ± 35 kg/m~3, which was similar to the density of ashes from straw combustion. Also the bulk densities were close to those reported for straw ashes. The flowability of the ashes was a little worse than the flowability of ashes from wood combustion. The measured heavy metal concentrations were below the usual limits for utilization of the ashes as soil conditioner. The concentrations in the bottom ash were similar to those reported for ash from forest residue combustion plants. In comparison with cyclone fly ashes from forest residue combustion the measured heavy metal concentrations in the cyclone fly ash were considerably lower. Cl-, S and Zn were enriched in the cyclone fly ash which is also known for ashes from wood combustion. In comparison with literature data obtained from Miscanthus plant material the concentrations of K, Cl-and S were lower.This can be attributed to the fact that the finest fly ash is not collected by the cyclone de-dusting system of the Miscanthus combustion plants. 相似文献
70.
In India coal combustion is the single largest source of emission of mercury which is a wide-spread persistent global toxicant, travelling across international borders through air and water. As a party to the Minamata convention, India aims to monitor and reduce Hg emissions and stricter norms are introduced for mercury emissions from power plants (30 μg/Nm3for flue gas in stack).This paper presents the results obtained during the experimental studies performed on mercury emissions at four coal-fired and one lignite-fired power plants in India. The mercury concentration in the feed coal varied between 0.12–0.27 mg/Kg. In the mercury mass balance, significant proportion of feed coal mercury has been found to be associated with fly ash, whereas bottom ash contained very low mercury. 80%–90% of mercury was released to air through stack gas. However, for circulating fluidised bed boiler burning lignite, about 64.8% of feed mercury was found to get captured in the fly ash and only 32.4% was released to air. The mercury emission factor was found to lie in the range of 4.7–15.7 mg/GJ. 相似文献