Fluorescence excitation-emission matrix combined with regional integration analysis to characterize the composition and transformation of humic and fulvic acids from landfill at different stabilization stages

Fluorescence excitation-emission matrix spectroscopy (EEMs) combined with fluorescence regional integration (FRI) analysis was used to investigate the composition and transformation of humic acid (HA) and fulvic acid (FA) from landfill. The EEMs of HAs at different landfill ages were characterized by two typical fluorescence chromophores with Ex/Em pairs at Ex = 420-470 nm/Em = 490-530 nm and Ex = 345-375 nm/Em = 450-465 nm. EEMs of FA were featured by other two distinctly different fluorophores with Ex/Em pairs at Ex = 315-335 nm/Em = 420-440 nm and Ex = 255-275 nm/Em = 425-455 nm. The results show that HA extracted from the refuse disposed in the year of 1989 was formed by connecting small-condensed aromatic structures with protein-like chains. Compared with HA extracted from the refuse disposed in the year of 1992, HA extracted from the refuse of 1996 had a higher fluorescence intensity and lower r_(B,A) (the ratio of the fluorescence intensities of peak B and peak A) value. It contained low molar mass components, low aromatic condensation degree, and more easily oxidized substituents. This indicates that the landfill time strongly affects the EEMs characteristics of HA, and that the humification degree of HA increases with the landfill time. A red shift to a longer wavelength region and an increase of fluorescence intensity were observed when the concentration of HA was increased, suggesting that concentration had a great influence on the fluorescence characteristics of HAs. pH (2-12) also had significant effects on the fluorescence intensity, although it exerted no effect on the peak position of fluorescence of HA and FA. The results of FRI show that increasing concentration lead to more interactions among various structure components and that small molecular weight units tend to aggregate or be masked into more complicated and larger structures. The pH influence on the fluorescence intensity of HA seems mainly through molecular configuration, while the fluorescence intensity change with pH may be due to various substituents of FA.     

高压脉冲放电与臭氧氧化联用降解水中对氯苯酚

研究高压脉冲放电与臭氧协同降解水中对氯苯酚影响因素的结果表明,250mg/L对氯苯酚处理30min后降解率达96%.臭氧浓度、自由基捕获剂以及电极之间的距离均可影响对氯苯酚的降解率.增加臭氧浓度及降低电极之间的距离,提高了对氯苯酚的降解率;加入自由基捕获剂,降低了对氯苯酚的降解率.     

酸雨对旱地红壤磷素释放的影响研究

为了探明酸雨对红壤磷素释放的诱导效应 ,采用室内模拟酸雨淋溶土柱的方法 ,研究了酸雨作用下旱地红壤磷素释放的特征与规律 .结果表明 ,从长期的淋溶效果来看 ,酸雨可促进红壤磷的释放 ,且酸雨pH值越低 ,磷累积释放量越大 ;磷释放的动态变化在不同土壤之间存在一定的差异 .红壤磷素的释放强度主要取决于土壤有效磷含量 ,而与阳离子交换量关系不大 .磷释放量与钙释放量相关性很弱 ,与铝释放量呈较强的正相关性 ,与铁释放量呈显著的正相关性 .酸雨对红壤磷释放的促进作用主要是由于酸雨对铁铝化合物尤其是铁化合物的溶蚀作用所至 .     

中国水路运输大气环境问题与防治对策

综述了中国水路运输中主要大气环境问题的现状，产生原因和环境影响，回顾了在防治技术和管理上的进展，并比较宏观提出了有关的防治对策和与ＭＡＲＰＯＬ国际公约接轨的建议。     

大气气溶胶酸度的研究进展

大气气溶胶的环境效应、气候效应和健康效应均与气溶胶的物理化学性质直接相关,其中大气气溶胶酸度是其重要的性质之一。大气气溶胶酸度对酸沉降、灰霾的形成具有重要作用,并影响大气非均相化学反应,相关研究已成为国际研究的热点。对国内外学者近年来在大气气溶胶酸度对大气环境与人体健康的影响、大气气溶胶酸度的影响因素与变化规律、大气气溶胶酸度/酸化缓冲能力的测定与计算方法、大气气溶胶酸性成分采集系统等方面的研究进展作了较系统的综述,并对大气气溶胶酸度研究未来的发展进行了展望。     

Levels and speciation of arsenic in the atmosphere in Beijing, China

Arsenic levels and speciation in the total suspended particles (TSPs) were quantitatively determined by high performance liquid chromatography on-line coupled with hydride generation atomic fluorescence spectrometry in Beijing, China from February 2009 to March 2011. The high TSP levels fluctuated between 0.07 and 0.79 mg m⁻³, with a mean level of 0.32 ± 0.17 mg m⁻³. The total arsenic concentrations ranged from 0.03 to 0.31 μg m⁻³ (mean: 0.13 ± 0.06 μg m⁻³) in Beijing‘s air. The concentrations of As(III) and As(V) ranged from 0.73 to 20 ng m⁻³ (mean: 4.7 ± 3.6 ng m⁻³) and from 14 to 2.5 × 10² ng m⁻³ (mean: 67 ± 35 ng m⁻³), respectively. As levels and speciation demonstrated relative higher levels in spring and autumn and lower values in summer and winter. As(V) accounted for 81-99% of the extractable species in the TSP samples which showed that As(V) was the major fraction of the extractable As. Organoarsenic species, monomethylarsonate (MMA) and dimethylarsinate (DMA) were not found in all samples. Higher values of enrichment factors demonstrated that arsenic in TSP mainly come from anthropogenic sources. High As and its species levels in air and respiratory exposure (0.30-0.84 μg d⁻¹) attributed to higher excess cancer risk ((4.2 ± 2.0) × 10⁻⁴) for people in Beijing.     

A2O氧化沟缺氧区三维流场模拟及结构形式优化

以FLUENT软件为工具,选用三维RNG k-ε紊流数学模型对重庆井口污水厂A2O氧化沟缺氧区内的流场进行模拟,分析了缺氧区内流场分布不均匀及沉泥的原因,提出了水下推进器的合理设置位置与导流墙的合理设置方式,并对优化后的缺氧区进行了模拟计算。通过优化后模拟的结果可见,在相同的功率密度下,缺氧区内的流场得到了较均匀的分布,流速从原来的0.131 m/s提升到0.204 m/s,减少了能量的损失。底部的流速也从原来的0.140 m/s提升到0.226 m/s,有效的防止或减少了沟中的污泥沉积。优化的结果对实际工程的设计也有一定的指导意义。     

A2O氧化沟缺氧区三维流场模拟及结构形式优化

以FLUENT软件为工具,选用三维RNG k-ε紊流数学模型对重庆井口污水厂A²O氧化沟缺氧区内的流场进行模拟,分析了缺氧区内流场分布不均匀及沉泥的原因,提出了水下推进器的合理设置位置与导流墙的合理设置方式,并对优化后的缺氧区进行了模拟计算。通过优化后模拟的结果可见,在相同的功率密度下,缺氧区内的流场得到了较均匀的分布,流速从原来的0.131 m/s提升到0.204 m/s,减少了能量的损失。底部的流速也从原来的0.140 m/s提升到0.226 m/s,有效的防止或减少了沟中的污泥沉积。优化的结果对实际工程的设计也有一定的指导意义。     

Water, heat, and airborne pollutants effects on transpiration of urban trees

Transpiration rates of six urban tree species in Beijing evaluated by thermal dissipation method for one year were correlated to environmental variables in heat, water, and pollutant groups. To sort out colinearity of the explanatory variables, their individual and joint contributions to variance of tree transpiration were determined by the variation and hierarchical partitioning methods. Majority of the variance in transpiration rates was associated with joint effects of variables in heat and water groups and variance due to individual effects of explanatory group were in comparison small. Atmospheric pollutants exerted only minor effects on tree transpiration. Daily transpiration rate was most affected by air temperature, soil temperature, total radiation, vapor pressure deficit, and ozone. Relative humidity would replace soil temperature when factors influencing hourly transpiration rate was considered.