大气压光电离技术及其在环境污染物分析中的应用

介绍了液相色谱-质谱联用(LC-MS)技术中新型软电离技术大气压光电离法(APPI)的基本原理、鼻子源结构以及电离的影响因素,综述了LC-APPI-MS在环境污染物定性定量分析中的应用.     

青岛市区春夏季大气能见度与颗粒物的关系

利用青岛市灰霾综合观测站2012年3月2日-2012年6月7日期间的监测数据,分析了青岛市区大气能见度与不同粒径颗粒物质量浓度的日变化特征,比较了各级别大气能见度下不同粒径颗粒物质量浓度及所占比例的相关性,研究了相对湿度对大气能见度和颗粒物质量浓度相关性的影响.结果表明,监测时段大气能见度与颗粒物质量浓度呈现较好的负相关,每天大气能见度最低值出现在早晨07:00--09:00;剔除相对湿度高于90％的前提下,PM2.5是影响大气能见度的主要因子,随着其在PM1o中所占比例上升,大气能见度级别不断下降,相关系数为-0.84;不同相对湿度区间下,PM2.5对大气能见度的影响最明显,其中,相对湿度为60％ ～ 70％,大气能见度与颗粒物质量浓度之间的相关性最好.     

南京市冬季大气颗粒态汞的分布特征

采集了南京市2012年冬季4个功能区的PM2．5、PM10、TSP样品,对不同粒径大气颗粒物中的颗粒态汞测试。结果表明,南京冬季大气颗粒物TSP中汞的质量浓度为49．26 pg/m3～257．14 pg/m3,平均质量浓度为161．27 pg/m3;PM10中汞的质量浓度为44．82 pg/m3～228．29 pg/m3,平均质量浓度为147．38 pg/m3;PM2．5中汞的质量浓度为35．98 pg/m3～178．58 pg/m3,平均质量浓度为104．10 pg/m3。不同功能区大气颗粒态汞质量浓度的分布趋势为：交通综合区＞旅游区＞住宿综合区＞商业区。大气颗粒态汞60％以上存在于可吸入肺的PM2．5中,细颗粒物富集汞的能力比粗颗粒物强。     

城市化进程中长江经济带长江干流水化学演变特征及影响因素

快速的城市化过程对城市周边水体水化学组成特征产生了诸多影响.为揭示长江经济带城市群发展对长江水化学特征的影响,于2020年10—11月沿长江干流,采集了四川宜宾至上海145个河流水样,并对比了历史水化学数据.同时,运用数理统计、离子比值法等方法探究了长江经济带平水期水化学特征.结果表明：长江河水的主要水化学类型为HCO₃·SO₄-Ca型,主要受流域内分布的碳酸盐岩等岩石风化作用控制;河水中阳离子以Ca²⁺为主,阴离子以HCO₃^-为主,Cl^-浓度沿径流方向升高,Ca²⁺和Mg²⁺浓度沿径流方向先升高后降低,SO₄^2-浓度沿径流方向逐渐上升,HCO₃^-浓度沿径流方向降低;城市化进程中,由于人类活动和工业活动加剧,除HCO₃^-外,Ca²⁺、Mg²⁺     

Watershed factors affecting stream acidification in the White Mountains of New Hampshire,USA

The streams tributary to acidic Cone Pond, pH 4.5–4.8, and circumneutral Black Pond, pH 5.3–6.4, in the White Mountains of New Hampshire, USA, were monitored for a year. The watersheds of these two ponds were characterized in terms of geology and stream hydrology. Chemical gradients and patterns in rock weathering and groundwater discharge explain many of the differences in mineral content and acidity of the streams. The rocks of Black watershed produced an average of ten times the equivalent of basic cations as rocks from Cone watershed. This is on the same order as the difference in acidity of the two streams. Down-stream changes in stream chemistry follow differing patterns, but reflect the same principle of residence time and water path length controlling chemical evolution of streamwater. Watershed and aquatic managers may use these parameters in an inexpensive and simple assessment of the susceptibility of individual streams and ponds to acidification. A method is recommended to determine quickly the potential influence of bedrock type to aquatic chemistry.     

SENSITIVITY OF HIGH-ELEVATION STREAMS IN THE SOUTHERN BLUE RIDGE PROVINCE TO ACIDIC DEPOSITION1

ABSTRACT: The Southern Blue Ridge Province, which encompasses parts of northern Georgia, eastern Tennessee, and western North Carolina, has been predicted to be sensitive to impacts from acidic deposition, owing to the chemical composition of the bedrock geology and soils. This study confirms the predicted potential sensitivity, quantifies the level of total alkalinity and describes the chemical characteristics of 30 headwater streams of this area. Water chemistry was measured five times between April 1983 and June 1984 at first and third order reaches of each stream during baseflow conditions. Sensitivity based on total alkalinity and the Calcite Saturation Index indicates that the headwater streams of the Province are vulnerable to acidification. Total alkalinity and p11 were generally higher in third order reaches (mean, 72 μeq/θ and 6.7) than in first order reaches (64 μeq/θ and 6.4). Ionic concentrations were low, averaging 310 and 340 μeq/θ in first and third order reaches, respectively. A single sampling appears adequate for evaluating sensitivity based on total alkalinity, but large temporal variability requires multiple sampling for the detection of changes in pH and alkalinity over time. Monitoring of stream water should continue in order to detect any subtle effects of acidic deposition on these unique resource systems.     

Evaluating the effectiveness of air quality management within the class I area of great smoky mountains national park

The Clean Air Act Amendments of 1977 designated national parks and wilderness areas larger than 1894 ha to be class I areas for air quality management, setting more restrictive criteria than the National Ambient Air Quality Standards. Class I areas are afforded the greatest degree of air quality protection under the Clear Air Act of 1970. In recent years, several studies have documented air pollution effects in the Great Smoky Mountains National Park (GSMNP), the second-largest class I area in the eastern United States. Air pollution problems of greatest concern in the GSMNP are effects of acid deposition, visibility impairment, and tropospheric ozone. Several recent events have increased concerns about air quality management in the class I area of the GSMNP. A forum, sponsored by the Southern Appalachian Man and the Biosphere Cooperative (SAMAB), was held in March 1992, which involved representative. parties-at-interest and began to address strategies for better management of air resources in the Southern Appalachians. This paper summarizes those discussions and recommendations and reports actions occurring as a result of the forum. Another objective of this paper is to present a conceptual framework for more effective management of the class I area of the GSMNP.     

COMPARATIVE WATER CHEMISTRY OF FOUR LAKES IN ROCKY MOUNTAIN NATIONAL PARK1

ABSTRACT: The inorganic chemistry of two pairs of lakes in Rocky Mountain National Park was studied to determine reasons for their similarities and differences. The pairs were located on differing geologic units. It was expected that weathering from the different types of parent material would cause differing cation concentrations between the pairs. This was verified by dissimilar concentrations of those cations which are products of primary weathering. Unexpected was a significant difference in anion concentrations between members of one pair having the same bedrock geology. This difference has been attributed to the presence of a wet sedge meadow above one of the lakes which serves as a biological filter for anions, particularly nitrate and sulfate. It is shown that small scale drainage characteristics which can alter regional atmospheric contributions are important contributors to lake chemistry.     

Patterns of Streamwater Acidity in Lye Brook Wilderness,Vermont, USA

Under the United States Clean Air Act Amendments of 1977, a class I designation safeguards wilderness areas from the negative effects of new sources of air pollution. We monitored streamwater chemistry in the class I Lye Brook Wilderness in southwestern Vermont from May 1994 through August 1995. Stream samples were collected biweekly at nine sampling locations throughout the wilderness and were analyzed for major cations and anions, dissolved organic carbon, pH, and acid-neutralizing capacity. Eight of nine sites sampled had mean annual acid neutralizing capacity values below zero. During the study period, decreases in streamwater acid neutralizing capacity values were caused primarily by SO₄ ²⁻. At some sites, however, NO₃ ⁻ and naturally occurring, weak organic acids were seasonally important. During high discharge, the low pH and high concentrations of inorganic monomeric Al were at levels that are toxic to acid-sensitive aquatic species. Watershed mass balances were calculated to determine annual gains or losses for measured ions. These budgets indicate that S inputs and outputs were nearly equal, there was a net loss of base cations, and a net gain in N. How long these watersheds can continue to assimilate additional N inputs is unknown.     

Chemical Changes in Sediment Pore-Waters of an Acidic Mining Lake After Addition of Organic Substrate and Lime for Stimulating Lake Remediation

In the past five years, enclosures have beeninstalled in an acidic mining lake in Lusatia to investigate insitu remediation processes. They were treated with straw, withstraw and Carbokalk, or with Carbokalk alone, where Carbokalkis a by-product of the sugar industry (solid precipitate ofnon-sugars after lime clarification of extracted sugar beetjuice). Sediment samples were taken as cores to get informationabout the behaviour of organic and inorganic components insediment pore-water with depth. Vertical distributions of pH,soluble reactive phosphate, nitrate, ammonium, silica,aluminium, iron, manganese, calcium, magnesium, sodium,potassium, sulphate, and DOC were measured. The resultingprofiles, each consisting of 15 data points at differentdepths, were compared by cluster analysis. The similarities ofsediment cores from different treated enclosures relating toprofiles of chemical components were discussed. Increasedconcentrations of potassium and sulphate were found in pore-water after substrate treatment. The data imply dissolution ofpotassium iron sulphate hydroxide minerals (jarosite) after anincrease of pH caused by dissolution of lime and by sulphatereducing processes which were stimulated by organic substrateaddition.