超高效液相色谱-质谱法测定地表水中丁基黄原酸

建立了直接测定水中丁基黄原酸的超高效液相色谱-电喷雾串联四极杆质谱法,无需对水样进行富集,水样过滤后就可直接测定。该方法简单、快捷、灵敏度高,方法检出限可达0.2μg/L。     

趋势分析法评价苯系物标准气体的时间稳定性

根据GB/T 15000.3—2008设计了苯系物标准气体的时间稳定性研究方案,制备了4瓶苯系物标准气体,随着时间的推移进行测定并将结果制图,结果显示量值随时间没有显著的变化趋势。以线性关系为模型,计算线性直线的斜率和斜率的标准偏差,用t检验判断斜率是否显著来评价标准气体的稳定性。计算结果显示,所有斜率均不显著,因此该研究制备的苯系物标准气体能够稳定保存22个月。根据时间稳定性数据计算由不稳定性引起的不确定度,并讨论了这种计算不稳定性引起不确定度的方法对结果有放大的可能性。     

Composition and source apportionment of PAHs in sediments at river mouths and channel in Kaohsiung Harbor, Taiwan

Fifty-eight sediment samples were collected in 2009 from the bottom of river mouths near Kaohsiung Harbor (Taiwan) and the harbor channel for the analyses of polycyclic aromatic hydrocarbons (PAHs) using gas chromatography-mass spectrometry (GC-MS). Concentrations of total PAHs varied from 39 to 30,521 ng g(-1) (dry weight); samples collected from the mouths of Love River, Canon River, Jen-Gen River, and Salt River showed the highest PAHs concentrations. This indicates that the major sources of sediment PAHs come from those polluted urban rivers and the harbor channel. In samples collected from the Salt River mouth, approximately 43% of the PAHs are identified as PAHs with 2 or 3 rings. However, samples collected from other locations contain predominantly PAHs with 4 rings (32 to 42%) or 5 and 6 rings (36 to 44%). Emissions from traffic-related sources and waste incineration contribute to the majority of PAHs found in most channel and river mouth sediments. However, coal/oil combustion is the main cause of high concentrations of PAHs observed in the Salt River mouth sediments. Principal component analyses with multivariate linear regression (PCA/MLR) have been used to further quantify the source contributions, and the results show that the contributions of coal/oil combustion, traffic-related and waste incineration are 37%, 33% and 30%, respectively.     

Investigation into organic phosphorus species in sediments of Baiyangdian Lake in China measured by fractionation and 31P NMR

Organic phosphorus (OP) species in sediments of the Baiyangdian Lake in China was investigated via fractionation and phosphorus-31 nuclear magnetic resonance ((31)P NMR) spectroscopy. Results of chemical fractionation showed that different OP fractions ranked in the order: humic acid-P?>?HCl-OP?>?fulvic acid-P?≈?NaHCO(3)-OP?>?residual OP. Labile OP and moderately labile OP, which can be degraded for phytoplankton uptake, contributed to 58.7-68.5% of total extracted OP, indicative of the potential P release from sediments in the lake. (31)P NMR spectroscopy results suggested the rank order of P species present in the NaOH-EDTA extractant of the sediments: orthophosphate?>?monoester-P?>?DNA-P?>?pyrophosphate-P. Phytate, polyphosphates, and phosphonates, which appeared in sediments of some deeper lakes, were not detected in the shallow lake. Significant correlations were identified between total P (TP) in water column and sediment TP, monoester-P and DNA-P, positively indicating that sediment P species, especially OP components, should probably contribute to the contents of P in water column and further to the lake eutrophication.     

Evaluation of rural wastewater treatment processes in a county of eastern China

With the rapid urbanization and industrialization in China, wastewater treatment in rural areas has become an increasing national concern. The selection of appropriate treatment processes closely based on the actual local status is crucial for the prevention of water quality deterioration in rural areas of China. This study presents a full year survey on the performances of various rural wastewater treatment processes at a county level in eastern China including seven three-chamber septic tanks (ST), five micro-power biological facilities (MP), seven constructed wetlands (CW), three stabilization ponds (SP) and five centralized activated sludge treatment plants (AS). It was found that although ST could remove a notable portion of total suspended solids (TSS) and chemical oxygen demand (COD(Cr)), it was ineffective in reducing nutrients and pathogens. Reliability and stability analyses showed that the centralized AS and decentralized CW processes outperformed the SP and MP processes. There were obvious discrepancies between the mean design concentrations, which ensure that 95% of the effluents meet the discharge standards, and the actual effluent concentrations determined for each process. The expected compliance with the tentatively adopted second-grade discharge standards (GB 18918-2002) was unsatisfactory for most of the water quality parameters examined, indicating an urgent need to design more practical discharge standards for decentralized treatment processes. Based on an overall assessment of reliability, stability and cost-effectiveness, the centralized AS was suitable for densely populated towns while the decentralized CW was suitable for sparsely populated villages.     

利用MALDI-TOF MS技术简便、快速检测水华蓝藻的方法研究

以水华蓝藻为研究对象,用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)技术对其进行测定分析并获得了蛋白质指纹图谱。对铜绿微囊藻标准株(NIES-843)样品通过3种前处理方法得到的质谱图进行对比,确定了质谱分析的样品前处理方法,建立了利用MALDI-TOF MS技术简便、快速检测水华蓝藻的方法。对在水华中出现的4种不同蓝藻进行MALDI-TOF MS分析,结果表明各种蓝藻具有其特征性波谱,可据此对水华蓝藻进行区分和鉴定。该方法快速、简便、精确、可程序化,具有广泛的应用前景。     

基于数值模式的环境空气质量预报影响因素和改进方法

数值预报是各地开展环境空气质量业务预报的主流预报方法之一。模式预报产品、基础输入资料、外部技术支持、主客观预报偏差和预报命中概率等诸多因素均会不同程度地影响数值模式预报效果,研究探讨了上述因素对数值模式预报效果的影响及其针对性的改进方法,以期降低预报偏差,改善业务预报整体效果,为各地提高业务预报质量提供方法思路和技术参考。     

西安市黑碳气溶胶浓度特征及与气象因素和常规污染物相关性

利用西安市环境监测站超级站2013年9月1日—2015年5月31日黑碳气溶胶(BC)的监测数据,研究空气中BC浓度特征及其与气象因素和常规污染物相关性。结果表明:BC小时平均浓度均值在春季、夏季和冬季的变化趋势呈"W"型,秋季呈"V"型,且冬季的第一个最低值和峰值比春季和夏季的分别延迟1 h和2~3 h,且20:00~次日6:00秋季BC小时平均浓度均值高于当年冬季。BC浓度在秋季和冬季较高,夏季较低。冬季BC/PM_(2.5)基本最低,秋季BC/PM_(2.5)相对最高。BC日平均浓度与气温、降水和风速的日平均值为极负显著相关,且风速小于1.0 m/s时,其与风速呈最显著的负相关。除O_3外,BC日平均浓度与其他常规空气污染物浓度呈显著相关,表明其同源性很强,且受机动车尾气排放的影响更大。     

2013年春夏季莱州湾海水环境要素特征和富营养化评估

根据2013年5（春季）、8月（夏季）莱州湾海水环境要素的调查资料,采用富营养化指数、潜在性富营养化评价模式和灰色聚类分析方法研究环境要素特征和评估海水富营养化状况。结果表明,无机氮是莱州湾水质的主要污染要素,春夏季的N/P平均值分别为100.76、117.84,潜在性富营养化评价模式结果表明,春夏季各站位的营养级均只包括Ⅳ_P、Ⅵ_P两类,磷限制为莱州湾的营养盐结构特征;富营养化指数评价结果表明,春季和夏季E>1站位比例分别为65%、20%;灰色聚类分析结果表明,春季Ⅱ级、Ⅲ级的站位比例分别为95%、5%,夏季Ⅱ、Ⅲ级的站位比例分别为70%、25%,Ⅱ级中的部分站位具有较大潜在富营养化风险。     

固相萃取-高效液相色谱法测地表水中11种酚类化合物

建立了固相萃取-高效液相色谱法同时测定地表水中11种酚类化合物的方法。水样经过全自动固相萃取仪富集,以HLB柱为萃取柱,乙腈(含1%乙酸)为洗脱剂,用高效液相色谱仪分析定量。该方法在0.5~5.0 mg/L范围内线性良好,相关系数为0.999 6~0.999 9,11种酚类化合物的纯水加标回收率为82.0%~111%,地表水加标回收率为98.5%~116%,精密度为3.58%~4.67%,检出限为1×10-4~5×10-4mg/L,该方法简单实用、准确可靠,可用于地表水中酚类化合物的同时测定。