福建泉州市东、西湖水体中氮的空间分布研究

初步探讨了东湖和西湖水体中氯的空间分布特征以及3种不同形态的氮与溶解氧的相关性.结果表明,(1)泉州东湖、西湖水体中总氮的平均含量分别为3.396、3.929mg/L,氨氮的平均含量分别为1.927、2.182mg/L,硝酸盐氮的平均含量分别为1.061、1.236mg/L,亚硝酸盐氮的平均含量分别为0.084、0.059 mg/L,东湖和西湖水体的主要氮素形式均是氨氮.(2)东湖出水口和位于动物园附近的采样点总氮、氨氮和亚硝酸盐氮浓度较其它采样点高,入水口、湖区北部及湖心区采样点的氨氤和硝酸盐氮的分布趋势基本一致.西湖东南部采样点总氮、氨氯、硝酸盐氯和亚硝酸盐氮的含量都较其它采样点高.(3)东湖水体的DO浓度与氨氛、硝酸盐氮和亚硝酸盐氯的含量都不具有相关性,而西湖水体的DO浓度与这3种形态氮显著相关.     

高效液相色谱法同时测定苯酚及其氯化中间产物

采用高效液相色谱法同时测定次氯酸钠氧化降解苯酚过程中苯酚及其5种氯化中间体，确定了检测波长，讨论了pH值对测定的影响。方法线性良好，苯酚、2-氯苯酚、4-氯苯酚、2，6-二氯苯酚、2，4-二氯苯酚、2，4，6-三氯苯酚的检出限分别为0．01mg／L、0．02mg／L、0．02mg／L、0．02mg／L、0．02mg／L、0．02mg／L，标准溶液测定的相对标准偏差≤0．8％，样品加标回收率为96．0％～102％。     

石墨炉原子吸收光谱法测定地面水中铝

用石墨炉原子吸收分光光度法,采用加入基体改进剂技术,建立了测定铝的原子吸收光谱分析的新方法。该方法的线性范围为0～20μg／L,检出限为0．042μg／L,相对标准偏差为1．51％,回收率为962％～101．6％．用于监测地面水中铝,获得满意结果。     

羊角铺水源水中极微量NO -2 - N的测定

建立了自制浮选器富集、分光光度法测定羊角铺水源水中痕量亚硝酸盐氮的方法，介绍了试验的注意事项。方法在0μg／L-4．00μg／L范围内线性良好，检出限为0．0002mg／L，RSD为2．0％-4．6％，加标回收率为94．0％-108％。     

高效液相色谱法测定水产品中四环素类抗生素残留

建立了固相萃取-高效液相色谱测定水产品中四环素类抗生素残留的方法，优化了前处理方法和色谱条件。方法在0mg／L-1．0mg／L范围内线性良好，四环素、土霉素和金霉素的检出限分别为0．02mg／kg、0．01mg／kg和0．05mg／kg，样品测定的RSD分别为6．8％、7．2％和8．5％，加标回收率分别为55．2％-81．0％、60．5％-70．5％和52．5％～73．5％。     

气相色谱法测定废水中苯胺类化合物

建立了气相色谱测定废水中5种苯胺类化合物的方法，优化了试验条件。方法在0mg／L-100mg／L之间线性关系良好，N，N-二甲苯胺、苯胺、对甲苯胺、间甲苯胺、邻甲苯胺的检出限分别为0．004mg／L、0．002mg／L、0．013mg／L、0．008mg／L、0．007mg／L，实际废水样品测定的RSD≤1．5％，加标回收率为93．8％～99．5％。     

变色酸比色法测定甲胺生产废水中甲醇

建立了变色酸比色测定甲胺生产废水中甲醇的方法，确定了最大吸收波长，优化了试验条件。方法在0mg／L-7．00mg／L范围内线性良好，检出限为0．07mg／L，标准溶液测定的RSD≤0．9％，废水样品的加标回收率为98．8％-101％。     

邻菲啰啉分光光度法测定海水中总铁

采用邻菲哕啉分光光度法测定海水中的总铁，方法在0mg／L～3．00mg／L范围内线性良好，检出限为0．03mg／L，相对标准偏差为3．0％，不同样品的加标回收率为95．2％～108％。     

邻菲哕啉分光光度法测定海水中总铁

采用邻菲哕啉分光光度法测定海水中的总铁，方法在0mg／L～3．00mg／L范围内线性良好，检出限为0．03mg／L，相对标准偏差为3．0％，不同样品的加标回收率为95．2％～108％。     

离子色谱法测定地表水中总氮

采用碱性过硫酸钾消解水样，OnGuardⅡBa柱萃取、过滤，去除消解液中大量硫酸盐，离子色谱法测定地表水中总氮含量。试验表明，方法在0ms／L～20．0mg／L之间线性良好，相关系数r为0．9994，方法检出限为0．007mg／L。该方法与国标法同时测定标准物质，测定值均在定值范围内，6次平行测定结果的RSD分别为2．3％和1．8％，地表水样的加标回收率为95．7％～105％。实际水样的测定结果与国标法比对，无明显差异。     

Use of multiple criteria for eutrophication assessment of coastal waters

The quality assessment of coastal waters of a tourist resort, on the basis of water quality criteria was attempted by using different quantitative approaches. Five variables related to eutrophication, that is nitrate, nitrite, ammonia, phosphate and chl were analyzed. Graphical methods were applied to all variables as well as unvariate statistical methods on the total inorganic nitrogen. Cluster analysis based on the five variables was also applied as an approach for numerical classification of the coastal waters. Comparison between the unvariate and multivariate methods used, was attempted to assess the validity of the procedures. The suitability of the methods used in coastal water management is also discussed.     

陕北石油勘探开发区地表水污染特征分析

研究了陕北主要石油勘探开发地区地表水的水质状况,分析了pH、矿化度(全盐量)、硬度、六价铬、砷、镉、铅、氨氮、挥发酚、石油类、化学需氧量(COD)、氯化物、硫酸盐、硝酸盐氮、总磷、氰化物、氟化物等17个指标,结果显示砷、镉、铅、氟化物、硝酸盐、氰化物、氟化物的P_i值均小于1;挥发酚、总磷、石油类、氨氮、COD、六价铬、硫酸盐、矿化度、氯化物、硬度均超标。研究区东部和西部地表水呈现出不同的污染特征,通过分析不同区域污染物来源,提出了污染防治对策与建议。     

Ground water discharge and the related nutrient and trace metal fluxes into Quincy bay,Massachusetts

Measurement of the rate and direction of ground water flow beneath Wollaston Beach, Quincy, Massachusetts by use of a heat-pulsing flowmeter shows a mean velocity in the bulk sediment of 40 cm d^–1. The estimated total discharge of ground water into Quincy Bay during October 1990 was 1324–2177 m³ d^–1, a relatively low ground water discharge rate. The tides have only a moderate effect on the rate and direction of this flow. Other important controls on the rate and volume of ground water flow are the limited thickness, geographic extent, and permeability of the aquifer. Comparisons of published streamflow data and estimates of ground water discharge indicate that ground water makes up between 7.4–12.1% of the gaged freshwater input into Quincy Bay. The data from this study suggest the ground water discharge is a less important recharge component to Quincy Bay than predicted by National Urban Runoff Program (NURP) models.The high nitrate and low nitrite and ammonia concentrations in the ground water at the backshore well sites and low nitrate and high nitrite and ammonia concentrations in the water flowing from the foreshore suggests that denitrification is active in the sediments. The low ground water flow rates and low nitrate concentrations in the foreshore samples suggest that little or no nitrate is surviving the denitrification process to affect the planktonic community. Similarly, oxidizing conditions in the aquifer and low trace metal concentrations in the ground water samples suggest that the metals may be precipitating and binding to sedimentary phases before impacting the bay.     

气相分子吸收光谱法在海水无机氮测定中的适用性研究

为探究气相分子吸收光谱法在海水无机氮测定中的适用情况，在检出限的10～20倍、30～50倍、50～100倍3个浓度范围内开展了准确度、加标回收率和方法比对试验。结果表明，采用气相分子吸收光谱法测定海水亚硝酸盐氮(0～0.100 mg/L)、硝酸盐氮(0～0.400 mg/L)、氨氮(0～0.200 mg/L)时，标准曲线均具有很好的线性，线性拟合度均在0.999 3以上，检出限依次为0.000 8、0.004、0.004 mg/L,且该方法不具有盐效应，适用于海水样品的检测。当样品浓度太低时，气相分子吸收光谱法测定结果的准确度较低，因此，建议仅在亚硝酸盐氮浓度高于0.030 mg/L、硝酸盐氮浓度高于0.100 mg/L、氨氮浓度高于0.090 mg/L时使用该方法，对应的海域为河口及近岸等无机氮含量较高的海域。此外，为保证测定结果的准确度，每个样品需平行测定2～3次。     

Quantitative detection of nitrate in water and wastewater by surface-enhanced Raman spectroscopy

The presence of inorganic nitrogen species in water can be unsuitable for drinking and detrimental to the environment. In this study, a surface-enhanced Raman spectroscopy (SERS) method coupled with a commercially available gold nanosubstrate (a gold-coated silicon material) was evaluated for the detection of nitrate and nitrite in water and wastewater. Applications of SERS coupled with gold nanosubstrates resulted in an enhancement of Raman signals by a factor of ～10⁴ compared to that from Raman spectroscopy. The new method was able to detect nitrate with linear ranges of 1–10,000 mg NO₃ ^?/L (R ²?=?0.978) and 1–100 mg NO₃ ^?/L (R ²?=?0.919) for water and wastewater samples, respectively. Among the common anions, phosphate appeared to be the major interfering anion affecting nitrate measurement. Nevertheless, the percentage error of nitrate measurement in wastewater by the proposed SERS method was comparable to that by ion chromatography. The nitrate detection limits in water and wastewater samples were about 0.5 mg/L. The SERS method could simultaneously detect sulfate, which may serve as a reference standard in water. These results suggested that the SERS coupled with nanosubstrates is a promising method to determine nitrate concentrations in water and wastewater.     

海洋水质在线监测系统中硝酸盐测量方法比较

硝酸盐是海洋水质监测的重要指标,目前在海洋水质在线监测系统中搭载的硝酸盐在线分析仪的种类较多,采用的测量原理也不尽相同.选取了 3种采用不同测量方法的代表性硝酸盐分析仪[氯化钒还原比色法硝酸盐分析仪、二乙烯三胺五乙酸还原比色法(DTPA)硝酸盐分析仪、紫外分光光度法硝酸盐分析仪],结合各自的测量原理、化学试剂特性等,就...     

Chemical monitoring and evaluation of the water quality of the Douro River at the Crestuma-Lever dam

Water taken from the Crestuma-Lever dam on the Douro River was evaluated considering the Portuguese Decree-law no. 236/98 of 1st August, 1998. This paper presents the metrological characteristics, validation of analytical methodologies and the data obtained from seasonal samplings. The test parameters selected are: temperature, pH, chloride, conductivity, carbon dioxide, alkalinity, hardness, oxidability, dissolved oxygen, BOD5, total suspended solids, sulfide, phosphate, silica, ammonium, nitrite, nitrate, sulfate, sodium, potassium, calcium, magnesium, iron, manganese, copper and zinc. From data analysis we can conclude that the water presented the following characteristics: a pH situated in the neutral zone; a median mineralization; a medium hardness; well oxygenated water; and a carbonate hardness exclusively due to bicarbonates. The temperature, pH, dissolved oxygen, ammonia, chlorides, sulfates, copper, zinc and BOD5 were compared with the legal limits presented in annexes XXI and I of Decree-law 236/98. The results relating to total hardness, nitrites, calcium, magnesium, sodium, potassium, aluminium, sulfides and oxidability were compared with the legal values in annex VI as there are no limits relating to these parameters in annexes XXI and I.     

基于顺序注射分析技术的总氮在线分析仪

针对环境监测领域,研制了一种基于顺序注射分析技术的总氮在线分析仪。该分析仪以注射泵为分析过程的液体驱动定量单元,以多通道选向阀为流路切换单元,以发光二极管和硅光电管为检测单元。在该分析平台上,含氮化合物在高温高压条件下经过硫酸钾氧化成硝酸根,硝酸根被还原为亚硝酸根后与N-(1-萘基)乙二胺盐酸盐生成偶氮染料,再由光电检测单元测定吸光度值,经计算得到总氮含量。与现有的总氮在线分析技术相比,该分析仪具有检测单元简单、生产成本低、测量精度高、试剂消耗和废液产生量少等优点,适合于环境监测等领域的长时间在线分析。     

Assessment of water systems for contaminants from domestic and industrial sewages

The State of Minas Gerais represents one of Brazil's most outstanding mining resources. The contamination of river waterfrom kaolin processing activities may be harmful to people inthe way of slow but chronic poisoning. On the other hand, the discharge of untreated or inadequately treated domestic sewage into aquatic environments can also cause deleterious effects to the health. However, no reliable figures are available for pollutant occurrences in river water. This draws attention to thevery precarious situation that exists with respect to pollutionby organic and inorganic toxic wastes, especially with respect to humans and fauna in all its expressions. Thus, with the purpose of establishing a preliminary report to trace out industrialisation outcomes, samples of river water, vegetation and fish were collected and analysed to detect pollutant inputs.The concentration of metals was determined in suspended particle,vegetation and fish, while those of nitrite, nitrate, phosphateand chloride were determined in river water samples. The concentration of dissolved oxygen (DO) was measured in river water at the time of collection. Chemical oxygen demand (COD) and biochemical oxygen demand (BOD) were also determined. Metalinputs in the samples analysed appeared to be related to effluentdischarges into the rivers. The suspended particles showed highconcentrations (in mg kg^-1) of zinc (62 600) and aluminium(559 000), while vegetation samples collected near rivers wereheavily contaminated with iron (7680). The fishes examined werecontaminated with chromium (1.5 mg kg^-1). In general, the concentrations of nitrite, nitrate, chloride, phosphate and BOD in river water were lower than the maximum values established bythe Brazilian Environmental Standards.     

A combinated approach to investigate the biochemistry and hydrography of a shallow bay in the South Adriatic Sea: the Gulf of Manfredonia (Italy)

The main goal of this study is to understand the hydrological and biochemical set up and processes of a marine coastal area located in the western side of the south Adriatic sea (the gulf of Manfredonia) by the use of both satellite images and in situ investigations A water sampling in the gulf of Manfredonia was performed at 18 fixed stations in June 2003; physico-chemical and biological parameters (temperature, salinity, dissolved oxygen and fluorescence) were measured along the water column and water samples were collected to analyse dissolved nutrients (ammonia, nitrite, nitrate, phosphate and silicate), total nutrients (nitrogen and phosphorus), chlorophyll a and total suspended solids. Surface spatial distributions of field collected data were examined to characterize biochemical and hydrographic conditions of the Gulf of Manfredonia and these results were related with the remote sensing analysis data. Remote sensed data (obtained by Landsat 7 TM and Modis Terra) were processed to obtain maps of chlorophyll a, temperature and optical characteristics of the gulf; these maps were compared to in situ data. From physico-chemical measurements no stratification was observed in the water column except for the south-eastern area. High concentrations of silicate and ammonia were observed in the northern zone of the gulf, while nitrate, phosphate, chlorophyll a and total suspended solids distributions showed higher values in the central coastal zone. These results were confirmed by remote sensing analysis; Modis elaboration showed a distribution with higher concentrations of chlorophyll a near the coast and Landsat images highlighted the extension of the surrounding agricultural areas crossed by the two main rivers which discharge into the gulf. The integration between field data with the remote sensing analysis showed to be a valid support in coastal zone management.