新疆石化工业区颗粒物含水量和酸度对二次无机组分形成的影响

大气二次污染物是新疆独山子区大气污染物的重要组成部分,研究大气中二次组分的转化过程对区域大气污染治理有着重要意义.对新疆独山子区2015年9月至2016年7月采集到的样品进行水溶性组分分析.结果表明,水溶性无机离子(TWSIs)表现出与PM_(2.5)一致的季节变化,为冬季(67.86μg·m~(-3))秋季(13.77μg·m~(-3))春季(10.09μg·m~(-3))夏季(4.85μg·m~(-3));冬季二次无机离子(NH~+_4、SO~(2-)_4和NO~-_3)占TWSIs的98%;结合气溶胶热力学模型(E-AIM)探讨独山子区大气颗粒污染物中颗粒相含水量以及颗粒酸碱性;表明独山子区颗粒物呈酸性,年均原位pH为0.81,其中冬季样品的pH(2.93)值最高;颗粒含水季节变化为冬季(331.32μg·m~(-3))秋季(5.91μg·m~(-3))春季(5.46μg·m~(-3))夏季(1.62μg·m~(-3));年均氮氧化率(NOR)和硫氧化率(SOR)分别为0.13和0.47,表明区域污染物存在二次转化;进一步分析表明颗粒相中的硫酸盐质量浓度受到颗粒含水量和颗粒酸碱度的影响较为明显;高的颗粒相含水条件下区域硝酸盐的形成主要以非均相反应为主.     

Effects of calcination temperature on physicochemical property and activity of CuSO4/TiO2 ammonia-selective catalytic reduction catalysts

CuSO_4/TiO_2 catalysts with high catalytic activity and excellent resistant to SO_2 and H_2 O,were thought to be promising catalysts used in Selective catalytic reduction of nitrogen oxides by NH_3.The performance of catalysts is largely affected by calcination temperature.Here,effects of calcination temperature on physicochemical property and catalytic activity of CuSO_4/TiO_2 catalysts were investigated in depth.Catalyst samples calcined at different temperatures were prepared first and then physicochemical properties of the catalyst were characterized by N2 adsorption-desorption,X-ray diffraction,thermogravimetric analysis,Raman spectra,Fourier-transform infrared spectroscopy,X-ray photoelectron spectroscopy,temperature-pro grammed desorption of NH_3,temperature-programmed reduction of H_2 and in situ diffuse reflectance infrared Fourier transform spectroscopy.Results revealed that high calcination temperature had three main effects on the catalyst.First,sintering and anatase transform into rutile with increase of calcination temperature,causing a decrement of specific surface area.Second,decomposition of CuSO_4 under higher calcination temperature,resulting in disappears of Br(?)nsted acid sites(S-OH),which had an adverse effect on surface acidity.Third,CuO from the decomposition of CuSO_4 changed surface reducibility of the catalyst and favored the process of NH_3 oxidation to nitrogen oxides(NO_x).Thus,catalytic activity of the catalyst calcined under high temperatures(≥600℃) decreased largely.     

新型内电解铁屑过滤塔在印染废水工业化规模处理中的应用

介绍了一种新型内电解铁屑过滤塔在印染废水工业化规模处理中的应用。在弱酸性条件下 ,该类型铁屑滤塔色度去除率高达 90 % ,废水可生化性提高 30 % ,运行一年半无板结和钝化现象。与后续的生化处理单元结合 ,出水稳定 ,实现达标排放。     

环状扩散管-分级采样器的建立和细粒子酸性的测定

建立了国内第一台扩散管－分级采样器，用来研究大气气胶溶胶的组成和细粒子的酸性，实验证明该采样系统能够有效地避免大气中的碱性物质对颗粒物采样的干扰。在北京，湖南等地进行了现场实验，测定了气溶胶的酸性。     

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

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.     

EFFECTS OF COAL PILE RUNOFF ON STREAM QUALITY AND MACROINVERTEBRATE COMMUNITIES1

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.     

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

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。     

牡蛎壳粉和石灰改良酸性水稻土对磷有效性、形态和酶活性的影响

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.     

大气气溶胶酸度和酸化缓冲能力研究

为了掌握大气气溶胶与酸性降水的关系 ,分析和研究了中国北方和南方不同观测点可吸入颗粒物 (PM10 )的酸度 ,并利用微量酸碱滴定的方法测定了其酸化缓冲能力。结果表明大气气溶胶具有一定的酸度 ,同时对酸化的缓冲能力非常低 ,甚至可以促进降水的酸化 ,这种污染特征也是上述观测点发生酸性降水的重要原因之一。     

Titration Curves: A Useful Instrument for Assessing the Buffer Systems of Acidic Mining Waters (10 pp)

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.