搅拌棒萃取-热脱附/气质联用法测定水中2-MIB和土臭素

采用搅拌棒萃取-热脱附/气质联用法测定水中2-甲基异莰醇和土臭素,优化了搅拌棒萃取和热脱附进样的条件。试验表明：两种目标化合物在1．00 ng/L～200 ng/L范围内线性良好,2-甲基异莰醇的相关系数为0．9993,土臭素的相关系数为0．9997,方法检出限分别为0．31 ng/L和0．15 ng/L;空白和实际样品的加标回收率为82．4％～116％,测定结果的RSD＜10％。     

工业链条炉燃用型煤与原煤颗粒物排放特征

选取燃烧型煤和原煤的典型链条炉,应用自行设计的固定源烟气颗粒物稀释采样系统,现场测试细颗粒物PM_(2.5)、PM_(10)和金属元素的排放特征。结果表明,型煤燃烧细颗粒物的排放比例高于原煤,型煤燃烧除尘器进口、出口PM_(2.5)质量比原煤燃烧分别增加715%和708%。燃烧型煤时,As和Pb在各粒径段的质量比均比原煤大。同时,由于型煤燃烧可吸入颗粒物的排放比例增加,包含或附着在烟尘上的金属元素排放比例也相应增加。     

Residue levels of hexachlorocyclohexane and dichlorodiphenyltrichloroethane in human milk collected from Beijing

Forty-eight human breast milk samples were collected from mothers in Beijing. The hexachlorocyclohexane (HCH) and dichlorodiphenyltrichloroethane (DDT) (including α-HCH, β-HCH, γ-HCH, δ-HCH, p,p′-DDE, p,p′-DDD, o,p′-DDT, and p,p′-DDT) contents of the samples were determined by gas chromatography/electron capture detection and gas chromatography/mass spectrometry. α-HCH, β-HCH, γ-HCH, p,p′-DDE, p,p′-DDD, and p,p′-DDT were detected at rates of 20, 100, 10, 100, 10, and 22 %, respectively. The average residue levels in the samples were 174.6 ng/g fat for β-HCH, 333.8 ng/g fat for p,p′-DDE, 6.57 ng/g fat for α-HCH, 7.67 ng/g fat for γ-HCH, 4.18 ng/g fat for p,p′-DDD, and 11.4 ng/g fat for p,p′-DDT. The results showed that the infants’ daily intake levels of HCH and DDT were 0.95 and 1.76 μg/kg body weight/day, respectively. Our result suggested that the total residue level of these organochlorine pesticides in breast milk from Beijing decreased and was lower than that from other coastal and heavy industrial cities in China. On the other hand, the levels of HCH and DDT were higher than those from some developed countries, but lower than those from other developing countries such as India.     

一种快速便捷的温室气体本底浓度采样方法初探

引入生态和气象研究领域的本底大气观测技术,提出一种便捷快速的温室气体本底浓度采样方法。该方法需要的设备简单,便于携带,能够快速完成采样。2011年5—7月,利用该方法,自西向东分别在处于我国三大阶梯的青藏高原东北缘、秦巴山区、长江中下游平原,选择不同类型的土地覆盖下垫面开展了地面采样实验,获得了33组以CO2和CH4为主的温室气体浓度数据。根据获得的采样结果,分别开展了人工采样数据分析及其与器测本底数据、卫星反演同期数据产品的对比分析,结果显示,几类数据趋势相符,数值相对偏差较低。总体认为,该方法获得的采样数据可靠、采样效率高,且成本低廉,这在我国温室气体自动监测站还比较少的现实情况下,不失为一种可选的快速便捷监测技术手段。     

Trace Metal Contents (Al, Cu and Zn) of Tea: Tea and Soil from Two Tea Plantations, and Tea Products from Different Provinces of China

The present project aims to investigate the possible contamination of teas with the trace metals: Al, Cu and Zn. Tea bushes sampled from two tea plantations in the northern part of Guangdong Province accumulated higher concentrations of Cu and Zn in young leaves, and of Al in old leaves. The analysis of the three metals in tea produced in different provinces indicated higher Al levels in those obtained from Guangdong and Yunnan Provinces, which may be due to the lower soil pH in these areas. Green tea had the lowest Al concentration among the four types of tea studied, as only the bud and two young leaves are used, whereas older leaves are used for other types of tea (black, Oolong and Puerh tea). The transfer of Al, Cu and Zn from soil to different parts of tea bushes was low in general, except for Zn at Lechang tea plantation which next to a Pb/Zn mine, where a higher transfer was observed from young leaves to tea products, indicating possible metal contamination during tea processing. However, low concentrations of Cu and Zn (less than 0.07 mg Cu L^-1 and 0.17 mg Zn L^-1), and moderate amounts of Al (2.1-2.5 mg L^-1) were obtained in the tea liquor (1% hot water extracts).     

Oxygen transfer in a full-depth biological aerated filter

The City of San Diego, California, evaluated the performance capabilities of biological aerated filters (BAFs) at the Point Loma Wastewater Treatment Plant. The City conducted a 1-year pilot-plant evaluation of BAF technology supplied by two BAF manufacturers. This paper reports on the first independent oxygen-transfer test of BAFs at full depth using the offgas method. The tests showed process-water oxygen-transfer efficiencies of 1.6 to 5.8%/m (0.5 to 1.8%/ft) and 3.9 to 7.9%/m (1.2 to 2.4%/ft) for the two different pilot plants, at their nominal design conditions. Mass balances using chemical oxygen demand and dissolved organic carbon corroborated the transfer rates. Rates are higher than expected from fine-pore diffusers for similar process conditions and depths and clean-water conditions for the same column and are mostly attributed to extended bubble retention time resulting from interactions with the media and biofilm.     

Feasibility of using microalgal biomass cultured in domestic wastewater for the removal of chromium pollutants

The feasibility of obtaining and using the biomass of a microalga, Chlorella miniata, from domestic wastewater (DW) cultures for the removal of chromium(III) [Cr(III)] and chromium(VI) [Cr(VI)] was compared with that from commercial Bristol medium (BM). Results showed that Chlorella miniata cultured in DW under 16-8 hours light-dark cycle [DW(16-8)] had similar growth to that in BM [BM(16-8)], but these two biomass had different biochemical compositions, and the former one had lower carbohydrate and higher protein content. When cultured in domestic wastewater, a higher biomass was obtained under continuous illumination [DW(24-0)], and the cells had higher carbohydrate and lower protein concentrations than that of DW(16-8). The spectra of the Fourier transform infrared spectrometer revealed that the functional groups on the surface of the three kinds of biomass--DW(16-8), DW(24-0), and BM(16-8)--were comparable, except an additional peak at 1731 cm(-1) was found in the biomass cultured in domestic wastewater, which was probably the result of bacterial contamination. Although biochemical differences were found among the three kinds of microalgal biomass, similar biosorption performances to chromium pollutants were recorded, with approximately 75% Cr(III) and 100% Cr(VI) removed at equilibrium in Cr(III) and Cr(VI) experiments, respectively, when dead biomass was used as a biosorbent. Therefore, it is possible to culture Chlorella miniata in domestic wastewater and use the biomass for the removal of chromium pollutants.     

Distribution and sources of polycyclic aromatic hydrocarbons in surface sediments of rivers and an estuary in Shanghai, China

Concentrations, spatial distribution and sources of 17 polycyclic aromatic hydrocarbons (PAHs) and methylnaphthalene were investigated in surface sediments of rivers and an estuary in Shanghai, China. Total PAH concentrations, excluding perylene, ranged from 107 to 1707 ng/g-dw. Sedimentary PAH concentrations of the Huangpu River were higher than those of the Yangtze Estuary. The concentration of the Suzhou River was close to the average concentration of the Huangpu River. PAHs source analysis suggested that, in the Yangtze Estuary, PAHs at locations far away from cities were mainly from petrogenic sources. At other locations, both petrogenic and pyrogenic inputs were significant. In the Huangpu and Suzhou Rivers, pyrogenic input outweighed other sources. The pyrogenic PAHs in the upper reaches of the Huangpu River were mainly from the incomplete combustion of grass, wood and coal, and those in the middle and lower reaches were from vehicle and vessel exhaust.     

二氧化锰氧化降解五氯酚的动力学模拟研究

研究了五氯酚(PCP)在二氧化锰(MnO2)氧化作用下的降解反应动力学,并讨论了无机离子和有机组分对PCP降解动力学的影响.采用n级反应速率模型对PCP降解动力学进行非线性拟合,结果显示n＞0.999,这表明一级反应速率模型适用于模拟PCP降解反应.在保证95%置信区间的条件下,采用准一级反应速率模型对0.5 h内的PCP降解动力学进行了非线性拟合,得到的离心法和维生素C破坏法下PcP降解表观速率常数kobs分别是2.86和2.14 h-1.二价金属离子的加入能降低PCP的kobs;当超过MnO2初始浓度2%以上的Mn2 存在时,Mn2 能对PCP的kobs产生显著影响,而其它不同类型和浓度的离子对kobs不产生显著影响.8种酚酸中的咖啡酸、丁香酸和五倍子酸对kobs的抑制作用达到了显著性水平;而肉桂酸、香豆酸、阿魏酸和邻(对)羟基苯甲酸的影响不明显.研究表明,降低PCP降解速率的主要原因是由于导致PCP在MnO2表面的吸附作用减弱或在MnO2表面与PCP发生竞争反应造成的.