长江口盐沼带湿地生态演替过程中甲烷排放研究

甲烷(CH4)作为河口湿地碳循环的重要中间产物,是大气中仅次于二氧化碳(CO2)的第二大温室气体,其排放清单对于全球气候变暖趋势的预测具有重要意义.因此,本研究采用静态箱-气相色谱技术,针对长江口盐沼带湿地CH4的排放通量展开了为期2年、每月1次的现场观测.研究结果表明,长江口盐沼带湿地持续表现为大气CH4的净排放源,其中,2011年在海三棱藨草覆盖情况下,全年CH4平均排放通量达到了1.00 mg·m-2·h-1,2012年互花米草大规模入侵后,海三棱藨草生物量显著减小,全年CH4排放通量减小为0.55 mg·m-2·h-1.Pearson相关性分析表明,沉积物有机碳含量、光合有效辐射及含水率等均不是影响长江口盐沼带湿地CH4排放的重要环境因子.在2011年,海三棱藨草生物量(p=0.001,r=0.928)、气温(p0.01,r=0.432)均与CH4排放通量呈现显著正相关,全年CH4最大排放通量出现在生物量最大的夏季8月份;2012年随着互花米草的入侵,CH4排放通量在5月份达到了最大值,自5月份之后逐渐减小,互花米草的入侵使长江口中潮滩盐沼带湿地CH4排放通量整体呈现出了下降的趋势.     

行业视角分要素环境经济综合测度分析研究

工业行业之间的污染负荷和产出效益的差异尚未得到足够关注.本文利用TOPSIS综合评价法,选取工业行业水、大气、产出等环境经济指标,分别测度污染负荷和产出效益的行业排名和变化趋势,并对重污染行业的水、大气污染负荷协调度进行综合评价,以揭示不同行业环境经济协调度变化情况.结果表明：不同要素的行业污染负荷差异显著,行业内的水、大气污染负荷呈现分化,行业环境经济协调度的结构和趋势变化明显,需区别对待不同行业不同要素的治污减排措施.     

Occurrence and impact of polychlorinated dibenzo-p-dioxins/dibenzofurans in the air and soil around a municipal solid waste incinerator

To assess the influence of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans(PCDD/Fs) on the environment in the vicinity of municipal solid waste incinerators(MSWIs), we determined the levels of PCDD/Fs in air and soil samples collected around a MSWI, which is the largest in China. The International Toxicity Equivalency Quantity(I-TEQ) concentrations of PCDD/Fs in air samples were from 0.0300 to 1.03 pg I-TEQ/m~3(0.445–13.6 pg/m~3), with an average of 0.237 pg I-TEQ/m~3, while in soil samples they ranged from 0.520 to 3.40 pg I-TEQ/g(2.41–88.7 pg/g) with an average of1.49 pg I-TEQ/g. The concentrations of PCDD/Fs in air and soil samples were comparable to other areas, and Pe CDFs were the dominant contributors, which was different from stack gas homologue patterns. Multivariate statistical analysis showed that PCDD/Fs emission from the MSWI did not directly affect the profiles of PCDD/Fs in air and soils, so that vehicles and unidentified emission sources should be considered. The daily inhalation levels of PCDD/Fs for children(0.0110 to 0.392 pg I-TEQ/(kg·day) and adults(0.00600 to 0.221 pg I-TEQ/(kg·day) near the MSWI were lower than the tolerable daily intake of 1.00 to 4.00 pg WHO-TEQ/(kg·day), but in winter the values were higher than in summer. These results can be used as basic data for assessing the risk of PCDD/Fs exposure in residents living around this MSWI, and more monitoring programs and studies should be carried out around MSWIs.     

基于主成分分析的河流水环境质量评价研究

主成分分析是多元统计分析的一个分支,它能够在保证原始数据信息损失最小的情况下,以少数的综合变量取代原有的多维变量,简化数据结构,客观确定权重,是环境质量综合评价的一种简单易行的方法.基于主成分分析理论,建立了水质综合评价模型,以南淝河为例,选取南淝河五个监测断面的九项监测指标作为评价因子,对南淝河的水环境质量进行综合评价.结果表明,南淝河流域水环境质量总体较差,有机污染物是造成南淝河水质污染的主要原因.     

地下水水源地保护区划分发展历程及方案、方法研究

介绍了国内外地下水水源地保护区建设的发展进程;综述了世界各国地下水水源地保护区区界的界定;同时阐述了目前国内外地下水水源地保护区划分的主要方法,重点剖析了经验法、计算半径法、矫正形状法、解析法、水文地质划分法和数值模拟法的特点和适用条件,并给出了各种方法所需要的数据资料;指出了地下水水源地保护区划分方法的发展趋势和研究方向.     

Carbonyl emissions from commercial cooking sources in Hong Kong

Cooking fumes are an important carbonyl emission source, especially in a highly urbanized city, such as Hong Kong. Cooking exhaust from 15 commercial kitchens of a variety of cooking styles was sampled and analyzed for a suite of 13 carbonyl compounds. Carbonyl compositions were varied among the different cooking styles. Formaldehyde was generally the most abundant carbonyl, and its contribution to the total carbonyl amount on a molar basis ranged from 12 to 60%. Acrolein was also found to be an abundant carbonyl in the cooking exhaust. The highest contribution by acrolein to the total carbonyls was found to be 30% in the exhaust of a western-style steak restaurant. Long-chain saturated carbonyls, that is, heptanal, octanal, and nonanal, accounted for a significant fraction (> 40%) of the total carbonyls in kitchens that always used heated cooking oils. Two dicarbonyls, glyoxal and methylglyoxal, had a various presence in the cooking emissions, ranging from negligible to 10%. The presence of benzaldehyde and tolualdehyde was mostly negligible in the sampled kitchen exhaust. Annual emission rates of both individual carbonyls and total carbonyls were estimated for various types of commercial kitchens. Local-style fast-food shops contributed the highest total carbonyl emissions per year mainly because of the large number of this kind of restaurant in Hong Kong. The citywide annual emission rates of the three most toxic carbonyls, formaldehyde, acetaldehyde, and acrolein, were estimated assuming that the limited number of sampled restaurants were representative of the average restaurants. Such estimates of carbonyl emission rates were comparable to the estimated carbonyl emissions from vehicular sources, suggesting the importance of commercial cooking as a source for carbonyls in Hong Kong.     

Polycyclic aromatic hydrocarbons in the surface soils from outskirts of Beijing, China

Surface soils from the outskirts of Beijing were analyzed for 16 priority polycyclic aromatic hydrocarbons (PAHs) using gas chromatography and mass spectrometry (GC-MS). The distribution map of total PAHs content was obtained as a contour plot. The concentration range of 16 PAHs varied by over two orders of magnitude from 0.016 microg g-1 in rural to 3.884 microg g-1 in suburban soils with the relatively standard deviation of 70.5%, showing large differences in the extent of PAHs pollution at the various sampling sites. It was notable that the concentration of BaP was 0.005-0.270 microg g-1 with a mean of 0.055 microg g-1. In general, the distribution of PAHs centered on the high molecular weight PAHs known to be carcinogenic. The 4-6 ring PAHs represented about 66% in rural samples and 70% in suburban soils of the total PAHs found. There was relatively good relationship among most of the individual PAHs and the compounds of Pyr, BaA, Flu, BbF, BaP, Chr and Ph gave strong correlation (r>0.8) with the sum of PAHs. The selected marked compounds, a principal component analysis (PCA) and special PAHs compound ratios (Ph/An vs Flu/Pyr; summation operator COMB/ summation operator EPA-PAHs) suggest the pyrogenic origins, especially traffic exhausts, are the dominant sources of PAHs in Beijing outskirts soils.     

贵阳市城区近地面PM10/PM2.5及重金属污染水平研究

2009年在贵阳市地区内设点采样.共采集了145个大气样品,对近地面大气颗粒物PM10/PM2.5的污染状况及其所含重金属进行调查.结果表明,贵阳PM10/PM2.5的污染严重,对人体健康危害很大;重金属元素分析中Pb和Zn的含量比较高,这些重金属元素更易于富集在细颗粒上,给环境带来了极大的潜在危险.最后文章提出了贵阳...     

Investigation of the decomposition reaction and dust explosion characteristics of crystalline dicumyl peroxide

The dicumyl peroxide (DCP) is widely used as a polymerization initiator, catalyst and vulcanizing agent in the chemical industry. A number of accidents have been caused by its thermal instability in storage or manufacturing process. Thus, its hazard characteristics have to be clearly identified. First of all, the differential scanning calorimeter (DSC) is used to measure the heat of decomposition reaction, which can contribute to understanding the reaction characteristics of DCP. The accelerating rate calorimeter (ARC) is used to measure the rates of temperature and pressure rises of decomposition reaction, and then the kinetics parameters are estimated. Furthermore, the MIKE 3 apparatus and the 20-l-Apparatus are used to measure and analyze the dust explosion characteristics of DCP at room temperature and atmospheric pressure. Finally, Semenov's thermal explosion theory is applied to investigate the critical runaway condition and the stability criterion of decomposition reaction, and to build the relationship of critical temperature, convective heat transfer coefficient, heat transfer surface area and ambient temperature. These results contribute to improving the safety in the reaction, transportation and storage processes of DCP.     

Quantum yield study of the photodegradation of hydrophobic dyes in the presence of acetone sensitizer.

The photodegradation of hydrophobic disperse dyes with different chromophores in the presence of acetone (ACE) was investigated. In this study, the photodecay of dyes was carried out in the Rayonet RPR-200 merry-go-round photoreactor, with 253.7 nm monochromatic ultraviolet (UV) lamps. A typical azo disperse dye (CI disperse yellow 7--DY7) and an anthraquinone disperse dye (CI disperse orange--DO11) were used as the probe compounds. The results demonstrate that the addition of acetone increases the solubility of hydrophobic disperse dyes and enhances the photosensitization reaction simultaneously. More than ten times of quantum yield enhancement is observed in the presence of ACE photosensitizer than in water alone. The photodegradation of DY7 and DO11 is dominated by photoreduction, which follows pseudo first-order decay, and the rate constants strongly depend on the solvent system (i.e., ACE/H2O ratios) and the initial pH levels. The decay quantum yields of dyes are normally observed with the increase of the ACE/H2O ratio. The optimum quantum yields of DY7 and DO11 were determined at 0.5 (v/v) and 0.25 (v/v), respectively, in alkaline conditions. A further increase in the ACE/H2O ratio reduces the quantum yields, possibly due to light attenuation by excess acetone.