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851.
采用电称冲击低压系统(ELPI)将无烟室和吸烟室内的空气颗粒物(0.03~10.00 μm)分成12级,对其粒子数和质量浓度进行测定.结果表明,吸烟室PM0.03~10.00的日平均粒子数和质量浓度分别是无烟室的1.50、1.13倍.烟草烟雾对室内颗粒物粒子数的影响集中在0.03~1.00 μm粒径段;对室内颗粒物质量浓度的影响表现为双模态结构,峰值分别在0.20~0.70、5.00~8.20 μm粒径段.烟草烟雾颗粒物的粒子数和质量浓度随烟雾消散时间的增加而减少,粒径越小,减小的越明显;烟草烟雾颗粒物在室内消散缓慢,会在长时间内造成影响,应引起足够关注. 相似文献
852.
重金属元素在冻土与融土中迁移的对比试验 总被引:1,自引:0,他引:1
随着寒区经济的发展,冻土地区的矿山开采活动不断加剧,随之产生的重金属污染问题也越来越严重.冻土地区生态环境脆弱,一旦受到破坏就很难恢复.针对此问题,室内模拟了尾矿矿渣在冻土与融土中的填埋及其对填埋场周边土体的影响,通过检测填埋场各处土壤的温度、含水量以及重金属元素的含量,发现温度和水分对重金属元素的迁移影响很大.土壤温度越低,重金属元素的迁移越慢;在温度梯度的作用下,重金属元素均随着水分从土体的暖端向冷端迁徙并聚集于冻结锋面.重金属元素在冻土中的迁移比融土中慢,表明冻土环境不利于重金属元素的迁移.在土壤质地、温度和含水量等相同的情况下,Zn的迁移性较强,Pb和Cu的迁移性相对较弱. 相似文献
853.
854.
855.
Cr(Ⅵ)污染土壤的热解还原无害化处理 总被引:4,自引:2,他引:2
提出了用热解还原法对含铬土壤进行无害化处理的新技术,研究了热解温度、热解时间及土壤有机质对铬无害化处理的影响,分析了热解前后土壤中铬的元素形态的变化.同时还探讨了热解还原过程中Cr(Ⅵ)的无害化机制.结果表明,土壤中的有机质在热解还原过程中产生的挥发分对Cr(Ⅵ)的无害化起核心作用;在200~600℃范围内,Cr(Ⅵ)的还原量随着热解温度升高而增大,500.0℃最适合于经济有效地实现Cr(Ⅵ)的热解还原处理;Cr(Ⅵ)的热解还原过程较快.铬的形态分析结果表明,热解后可交换态和碳酸盐结合态铬量大大降低,大部分铬转化成了活性低的残渣态,极大地降低了铬的危害. 相似文献
856.
857.
为了脱除CO2温室气体,提出了利用氨水土壤混合物去除CO2的新方法。分别考察了土壤颗粒粒径、CO2初始流量、氨水浓度(质量比)和温度对CO2脱除量和脱除率的影响。实验结果表明,该方法去除CO2的量较土壤物理吸附量和氨水化学吸收量的总和提高了大约15%;随着氨水浓度的增大,CO2的脱除率和脱除量都增大;随着土壤颗粒粒径和CO2初始流量的增大,CO2的脱除率和脱除量都减小;当温度由22℃升高到31℃,CO2的脱除率随着温度的升高而增大,但是继续升高温度到40℃,CO2的脱除率反而下降。 相似文献
858.
Sun Yang Wang Yuesi Zhang Changchun 《Atmospheric environment (Oxford, England : 1994)》2009,43(2):468-472
This paper reports altitude-resolved concentrations of sulfur dioxide (SO2) and particulate matter up to 10 microns in diameter (PM10) in the planetary boundary layer of major urban centers during extreme pollution episodes. The concentration of SO2 was observed continuously from November 24, 2004, to December 4, 2004, in Beijing during the heating period. Fluorescence SO2 analyzers were used to measure the atmospheric SO2 concentrations. Four SO2 analyzers were placed at 4 different levels (8 m, 47 m, 120 m, and 280 m) of the 325-m high meteorological observation tower of the Institute of Atmospheric Physics (IAP), Chinese Academy of Sciences. A maximal SO2 concentration of 172.3 ppb was measured during this pollution episode, and SO2 concentration increased with altitude and reached its maximal value at ~50 m. The study also analyzed the meteorological situation before, during, and after the pollution episode. 相似文献
859.
J.M. Zhang T. Wang A.J. Ding X.H. Zhou L.K. Xue C.N. Poon W.S. Wu J. Gao H.C. Zuo J.M. Chen X.C. Zhang S.J. Fan 《Atmospheric environment (Oxford, England : 1994)》2009,43(2):228-237
Knowledge on atmospheric abundance of peroxyacetyl nitrate (PAN) is important in assessing the severity of photochemical pollution, and for understanding chemical transformation of reactive odd nitrogen and its impact on the budget of tropospheric ozone (O3). In summer 2006, continuous measurements of PAN were made using an automatic GC–ECD analyzer with an on-line calibrator at a suburban site of Lanzhou (LZ) and a remote site of Mt. Waliguan (WLG) in western China, with concurrent measurements of O3, total reactive nitrogen (NOy) and carbon monoxide (CO). At LZ, several photochemical episodes were observed during the study, and the average mixing ratio of PAN (plus or minus standard deviation) was 0.76 (±0.89) ppbv with the maximum value of 9.13 ppbv, compared to an average value of 0.44 (±0.16) ppbv at remote WLG. The PAN mixing ratios in LZ exhibited strong diurnal variations with a maximum at noon, while enhanced concentrations of PAN were observed in the evening and a minimum in the afternoon at WLG. The daily O3 and PAN concentration maxima showed a strong correlation (r2 = 0.91) in LZ, with a regression slope (PAN/O3) of 0.091 ppbv ppbv?1. At WLG, six well-identified pollution plumes (lasting 2–8 h) were observed with elevated concentrations of PAN (and other trace gases), and analysis of backward particle release simulation shows that the high-PAN events at WLG were mostly associated with the transport of air masses that had passed over LZ. 相似文献
860.
Zhi-Ping Wang Yang Song Jay Gulledge Qiang Yu Hong-Sheng Liu Xing-Guo Han 《Atmospheric environment (Oxford, England : 1994)》2009,43(13):2148-2153
A budget for the methane (CH4) cycle in the Xilin River basin of Inner Mongolia is presented. The annual CH4 budget in this region depends primarily on the sum of atmospheric CH4 uptake by upland soils, emission from small wetlands, and emission from grazing ruminants (sheep, goats, and cattle). Flux rates for these processes were averaged over multiple years with differing summer rainfall. Although uplands constitute the vast majority of land area, they consume much less CH4 per unit area than is emitted by wetlands and ruminants. Atmospheric CH4 uptake by upland soils was ?3.3 and ?4.8 kg CH4 ha?1 y?1 in grazed and ungrazed areas, respectively. Average CH4 emission was 791.0 kg CH4 ha?1 y?1 from wetlands and 8.6 kg CH4 ha?1 y?1 from ruminants. The basin area-weighted average of all three processes was 6.8 kg CH4 ha?1 y?1, indicating that ruminant production has converted this basin to a net source of atmospheric CH4. The total CH4 emission from the Xilin River basin was 7.29 Gg CH4 y?1. The current grazing intensity is about eightfold higher than that which would result in a net zero CH4 flux. Since grazing intensity has increased throughout western China, it is likely that ruminant production has converted China's grazed temperate grasslands to a net source of atmospheric CH4 overall. 相似文献