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排序方式: 共有103条查询结果,搜索用时 15 毫秒
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东莞市大气亚微米粒子PM1及其中水溶性无机离子的污染特征 总被引:3,自引:2,他引:1
2011年8月—2012年7月期间,利用中流量(100 L·min-1)大气采样器对东莞市A和B两点(A:生活区,B:工业区)进行PM1、PM1~2.5、PM2.5~10采样,并定量分析颗粒物上F-、Cl-、NO-3、SO2-4、NH+4、Na+、K+、Ca2+、Mg2+等9种水溶性无机离子.分析结果显示,工业区B点的细粒子污染较生活区A点严重,B点PM1质量浓度年均值为48μg·m-3,其浓度是A点的1.2倍.A、B两点PM1对PM2.5和PM10的质量贡献率无明显差异,平均贡献率分别高达69%和45%.二次离子SO2-4、NO-3、NH+4及与燃烧行为有关的K+、Cl-等5种离子在细粒子PM1上富集,这5种离子对PM1质量的贡献率分别为18.82%~19.76%、4.98%~5.47%、3.98%~4.12%、2.03%~2.27%和3.39%~3.78%.而其他4种离子,Ca2+、Mg2+、F-和Na+积聚在粗粒子PM2.5~10上.PM10/PM2.5/PM1三种粒子中,PM1粒子酸性值AE/CE(阴离子当量浓度/阳离子当量浓度)比值和硫转化率SOR、氮转化率NOR值均是最高. 相似文献
4.
用两种土壤研究土壤与酸的反应时间对土壤酸度及土壤溶液中铝离子形态分布的影响。结果表明,土壤溶液pH随反应时间增加而增加,安徽红壤pH的增幅大于江西红壤。在pH3.0的HNO3溶液中,土壤溶液中的总铝及Al3 均随反应时间增加而减少,而在pH3.5的HNO3溶液中,土壤溶液中总铝及Al-F络合物先随反应时间的增加而减小.然后又有所增加。 相似文献
5.
Michael C. Swift 《Journal of the American Water Resources Association》1985,21(3):449-457
Samples of coal pile runoff, Georges Creek water, and macrobenthos above and below two coal storage areas along Georges Creek, Allegany County, Maryland, were collected in July, August, and September 1982, and February and July 1983. Coal pile runoff was collected under high- and low-flow conditions. Water samples were analyzed for Hg, Zn, As, Fe, Mn, Al, SO4?2, pH, filterable and non-filterable residue, conductivity and acidity. Leachate from coal piles along Georges Creek contained high concentrations of heavy metals, particularly manganese, aluminum and zinc. Iron and sulfate were very high and the pH ranged from 1.4 to 3.1. Georges Creek water had much lower concentrations of metals, iron and sulfate and a pH of about 7.0. The distribution of macrobenthos in Georges Creek showed the effects of both runoff from coal storage piles and periodic drought. Brillouin's diversity index values were low even in areas which did not dry. Densities of tubificid worms and chironomid larvae were very high above the coal storage areas where organic inputs were high. At all the rest of the sampling stations, macroinvertebrate densities were very low. Where coal pile runoff enters Georges Creek, it compounds the effects of periodic drought and further stresses the aquatic community. 相似文献
6.
我国南方粮食主产区土壤酸化治理是提升耕地地力促进粮食增产的重要内容,目的是探究酸化土壤改良剂牡蛎壳粉和石灰对水稻土酸度、磷有效性和形态以及酶活性和相关功能基因的影响.盆栽试验设计2种改良剂的3个施用量(0.05%、0.10%和0.15%),以水稻为试验作物.结果表明:①牡蛎壳粉和石灰均显著提高土壤pH,降低土壤交换性酸,且改良效果随着改良剂用量增加而提高,相同用量下石灰对土壤酸性的改良效果高于牡蛎壳粉;② 4种有效磷提取剂提取的土壤有效磷测定结果表明,牡蛎壳粉和石灰显著提高H2SO4-P、Bray-1 P和Olsen-P含量,其中Olsen-P含量随改良剂用量的增加而提高.③土壤中不同形态无机磷含量表现为:Fe-P>Al-P>Ca-P,石灰和牡蛎壳粉显著提高Al-P和Fe-P含量,分别提高26.3%~37.4%和7.9%~23.7%;0.15%改良剂显著增加Ca-P含量;④石灰和牡蛎壳粉对土壤DHA、ALP、IPP活性和phoD基因拷贝数具有提高作用,而对土壤ACP活性、phoC和pqqC拷贝数表现为降低;⑤改良剂(0.10%和0.15%)显著提高水稻产量,0.15%用量的石灰和牡蛎壳粉分别提高水稻产量34.2%和46.8%,但对秸秆生物量无显著影响.相关分析表明,土壤无机磷和有效磷含量与pH和ALP活性呈显著正相关,改良剂通过消除土壤酸化和提高土壤磷酸酶活性来改善土壤磷营养状况,这对促进作物产量具有积极作用. 相似文献
7.
Totsche O Fyson A Kalin M Steinberg CE 《Environmental science and pollution research international》2006,13(4):215-224
Background, Aims and Scope The acidification of mine waters is generally caused by metal sulfide oxidation, related to mining activities. These waters
are characterized by low pH and high acidity due to strong buffering systems. The standard acidity parameter, the Base Neutralization
Capacity (BNC) is determined by endpoint titration, and reflects a cumulative parameter of both hydrogen ions and all buffering
systems, but does not give information on the individual buffer systems. We demonstrate that a detailed interpretation of
titration curves can provide information about the strength of the buffering systems. The buffering systems are of importance
for environmental studies and treatment of acidic mining waters.
Methods Titrations were carried out by means of an automatic titrator using acidic mining waters from Germany and Canada. The curves
were interpreted, compared with each other, to endpoint titration results and to elemental concentrations contained therein.
Results and Discussion The titration curves were highly reproducible, and contained information about the strength of the buffer systems present.
Interpretations are given, and the classification and comparison of acidic mining waters, by the nature and strength of their
buffering systems derived from titration curves are discussed. The BNC-values calculated from the curves were more precise
than the ones determined by the standard endpoint titration method. Due to the complex buffer mechanisms in acidic mining
waters, the calculation of major metal concentrations from the shape of the titration curve resulted in estimates, which should
not be confused with precise elemental analysis results.
Conclusion Titration curves provide an inexpensive, valuable and versatile tool, by which to obtain sophisticated information of the
acidity in acidic water. The information about the strength of the present buffer systems can help to understand and document
the complex nature of acidic mining water buffer systems. Finally, the interpretation of titration curves could help to improve
treatment measurements and the ecological understanding of these acidic waters. 相似文献
8.
鼎湖山针阔叶混交林土壤酸度与土壤养分的季节动态 总被引:4,自引:1,他引:4
研究了鼎湖山南亚热带森林演替系列中处于中间阶段的针阔叶混交林土壤的pH值、水解氮、速效磷、钾、交换性钙、镁等几种营养元素的含量现状及季节动态。结果表明:混交林土壤为强酸性土壤,表层(0--20cm)土壤酸度高于中(20--40cm)、下(40-60cm)层土壤,0~40cm土壤pH值具有明显的季节波动性。降雨、温度、凋落物、植物根系以及微生物的活动等因素可能是鼎湖山混交林土壤pH值季节动态变化的主要因素。除Ca外,在同一剖面内,表层土壤养分的含量明显高于中下层,而中下层之间相差不大,养分大多在冬季较高,随着季节变动(1,4,7,10月)呈下降趋势。 相似文献
9.
This study investigated geochemical characteristics of the acid mine drainage (AMD) discharged from the abandoned mine adits in the vicinity of the Dogye coal mine in Korea. Acid mine drainage discharged from Jeoncha pit adit of the Dogye coal mine, which is the main source of the AMD in the study area, had a pH value of 3.0 and concentrations of 2148mg SO4
2– L–1, 229mg Fe L–1, 71mg A1 L–1 and 11mg Mn L–1. The reduction of some metal concentrations downstream from the discharge point could be explained on the basis of dilution and precipitation. The order of removal of metal ions downstream from the discharge point was Fe>A1, Cu>Zn, Mn. Acidity could be used as a good determining factor offering comprehensive and quantitative values for the polluting extent of acid mine drainage. The acidities existing in all acidic water samples in the Gunahan district originated primarily from mineral acidity, especially in the upper Nahan Creek from dissolved Fe and Al and in the middle and down Nahan Creek from dissolved Al. From the application of the WATEQ4F program, it was determined that predominant species of dissolved Fe in all water samples was Fe2+, and those of dissolved Al were AlSO4
+ and Al3+ except for IW2 sample which was associated with white precipitates. The species of dissolved Al in IW2 sample include also AlOH2+ and Al(OH)2
+. The saturation indices of goethite and haematite were positive in the water samples associated with ochrous precipitates (usually called Yellow Boy), therefore these solids might be precipitated. For the IW2 sample, the saturation indices of amorphous Al(OH)3 and gibbsite were positive, so theoretically these solids might also be precipitated. By XRD analysis, it was found that goethite occurs in ochrous precipitates, and gibbsite in white precipitates. 相似文献
10.
Ci Zhang Xiaohui Lu Jinghao Zhai Hong Chen Xin Yang Qi Zhang Qianbiao Zhao Qingyan Fu Fei Sh Jing Jin 《环境科学学报(英文版)》2018,30(10):118-132
To investigate formation mechanisms of secondary organic carbon(SOC) in Eastern China,measurements were conducted in an urban site in Shanghai in the summer of 2015. A period of high O_3 concentrations(daily peak 120 ppb) was observed, during which daily maximum SOC concentrations exceeding 9.0 μg/(C·m~3). Diurnal variations of SOC concentration and SOC/organic carbon(OC) ratio exhibited both daytime and nighttime peaks. The SOC concentrations correlated well with O_x(= O_3+ NO_2) and relative humidity in the daytime and nighttime, respectively, suggesting that secondary organic aerosol formation in Shanghai is driven by both photochemical production and aqueous phase reactions. Single particle mass spectrometry was used to examine the formation pathways of SOC. Along with the daytime increase of SOC, the number fraction of elemental carbon(EC) particles coated with OC quickly increased from 38.1% to 61.9% in the size range of 250–2000 nm, which was likely due to gas-to-particle partitioning of photochemically generated semi-volatile organic compounds onto EC particles. In the nighttime, particles rich in OC components were highly hygroscopic, and number fraction of these particles correlated well with relative humidity and SOC/OC nocturnal peaks. Meanwhile, as an aqueous-phase SOC tracer, particles that contained oxalate-Fe(III) complex also peaked at night. These observations suggested that aqueous-phase processes had an important contribution to the SOC nighttime formation. The influence of aerosol acidity on SOC formation was studied by both bulk and single particle level measurements, suggesting that the aqueous-phase formation of SOC was enhanced by particle acidity. 相似文献