致癌物苯并(a)芘[Benzo(a)Pyrene]对土壤--植物系统污染研究

本报告是1973—1979年研究工作的简要总结.采用野外调查、盆钵试验、放射性示踪同位素、荧光分光光度计、人工模拟控制大气污染实验与电镜扫描照相等方法,研究了在石油污水灌溉条件下,环境中致癌物苯并(a)芘(B(a)P)对水稻可食部分的影响.其结果是:①土壤表层(0—15cm)B(a)P含量在<10—500ppb范围内,污水与清水灌区栽培水稻精白米中B(a)P的含量无显著差异;②水稻各部分的B(a)P来自大气污染、水——土壤污染以及水稻本身生物合成.B(a)P在水稻体内的分配次序为:根系≥茎叶>皮壳≥籽实,水稻精白米中B(a)P含量约0.18ppb;③在自然条件下,水稻的外来B(a)P污染源主要是大气飘尘,而水——土壤是次要的.     

关于海洋资源的资产属性与资产化管理

通过对海洋资源的基本特性分析,论证了海洋资源的资产属性和把海洋资源纳入资产化管理的合理性,并从宏观与微观两个层面对海洋资源进行资产化管理的有关核算问题作了探讨。指出只有合理的海洋资源核算,才能明确界定海洋资源产权,实现海洋资源的高效利用。     

Distribution characteristics of poly- and perfluoroalkyl substances in the Yangtze River Delta

In this work, a method was developed and optimized for the analysis of polyfluoroalkyl and/or perfluoroalkyl substances(PFASs) content in surface water and sediment samples with high instrumental response and good separation. Surface water and sediment samples were collected from the Yangtze River Delta(YRD) to analyze the distribution characteristics of perfluoroalkyl carboxylic acids(PFCAs), perfluoroalkane sulfonic acids(PFSAs), perfluoroalkyl phosphonic acids(PFPAs), perfluoroalkyl phosphinic acids(PFPiAs), and polyfluoroalkyl phosphoric acid diesters(di PAPs). The results showed that the total concentrations of PFCAs and PFSAs in YRD varied from 31 to 902 ng/L. PFCAs(≥ 11 carbons) and PFSAs(≥ 10 carbons atoms) were not detected in any surface water samples. The mean concentrations of all PFCAs and PFSAs in surface water from the sampling areas decreased in the following order:Yangtze river(191 ng/L) ≈ Taihu lake(189 ng/L) Huangpu river(122 ng/L) ≈ Qiantang river(120 ng/L) Jiaxing urban river(100 ng/L). Strong significant(p 0.05) correlations between the concentrations of many of the compounds were found in the sampling areas, suggesting a common source for these compounds. Only perfluorooctanoic acid(PFOA) was observed in all sediment samples, at concentrations varying from 0.02 to 1.35 ng/g. Finally, detection rates of two di PAPs were only 8% and 10%, respectively and the concentration of di PAPs was two to three times lower compared to PFCAs and PFSAs.     

Applying a new method for direct collection,volume quantification and determination of N2 emission from water

The emission of N2 is important to remove excess N from lakes, ponds, and wetlands. To investigate the gas emission from water, Gao et al.(2013) developed a new method using a bubble trap device to collect gas samples from waters. However, the determination accuracy of sampling volume and gas component concentration was still debatable. In this study, the method was optimized for in situ sampling, accurate volume measurement and direct injection to a gas chromatograph for the analysis of N2 and other gases. By the optimized new method, the recovery rate for N2 was 100.28% on average; the mean coefficient of determination(R2) was 0.9997; the limit of detection was 0.02%. We further assessed the effects of the new method, bottle full of water, vs. vacuum bag and vacuum vial methods, on variations of N2 concentration as influenced by sample storage times of 1,2, 3, 5, and 7 days at constant temperature of 15°C, using indices of averaged relative peak area(%) in comparison with the averaged relative peak area of each method at 0 day.The indices of the bottle full of water method were the lowest(99.5%–108.5%) compared to the indices of vacuum bag and vacuum vial methods(119%–217%). Meanwhile, the gas chromatograph determination of other gas components(O2, CH4, and N2O) was also accurate. The new method was an alternative way to investigate N2 released from various kinds of aquatic ecosystems.     

“十五”期间沈阳市经济发展与环境保护的相互促进分析

论述了沈阳市“十五”期间经济发展及能源消耗的变化趋势,在阐述城市建设对环境保护的促进作用及“十五”期间沈阳市环境质量变化趋势的基础上,对沈阳市经济发展与环境质量的相互促进进行了分析。     

Hexabromocyclododecane and tetrabromobisphenol A in sediments and paddy soils from Liaohe River Basin, China: Levels, distribution and mass inventory

Hexabromocyclododecane(HBCD) and tetrabromobisphenol A(TBBPA) are two kinds of brominated flame retardants and widely present in the environment and biota. The levels,spatial distributions and mass inventories of HBCD and TBBPA were investigated in sediments and paddy soils from the Liaohe River Basin in northeast China. The concentrations of ΣHBCD and TBBPA were in the range of not detected(nd) to 4.02 ng/g dry weight(dw) and 0.03 to 4.06 ng/g dw, respectively. γ-HBCD was dominated in sediments,while the abundance of α-HBCD was relatively high in paddy soils. The spatial distributions of HBCD and TBBPA in surface sediments and paddy soils indicated that the local point-input was their major source. The significant correlation between total organic carbon(TOC) contents and the HBCD levels suggested that TOC content also exerted an influence on the distribution of HBCD in sediments. Meanwhile, it was found that the irrigation with river water was not the major transportation pathway of HBCD and TBBPA in paddy soils. Based on the study, it was estimated that there were about 1.67 tons HBCD and 2.20 tons TBBPA deposited into sediments of the Liaohe River system every year. The total mass inventories of HBCD and TBBPA in sediments were far higher than that in paddy soils.     

新型堆肥调理剂的吸水特性及应用

本文研究新型堆肥调理剂 (CTB堆肥调理剂 )的吸水特性及其应用效果。结果表明 ,调理剂的吸水平衡时间为8h。CTB调理剂的混料比例为 4 0 %～ 6 0 % ,可以将污泥水分调节到较为理想的范围 ,使堆肥过程能顺利完成。本调理剂具有适合于快速堆肥和自动控制、可降低堆肥过程的能耗、吸水性较强、除臭效果好、价格便宜、可以循环利用、易于筛分等优点 ,是城市污泥等有机废弃物工厂化快速堆肥的理想调理剂     

The thermal transformation mechanism of chlorinated paraffins: An experimental and density functional theory study

The increasing production and usage of chlorinated paraffins(CPs) correspondently increase the amount of CPs that experience thermal processes. Our previous study revealed that a significant amount of medium-chain chlorinated paraffins(MCCPs), short-chain chlorinated paraffins(SCCPs) as well as aromatic and chlorinated polycyclic aromatic hydrocarbons(Cl-PAHs) were formed synergistically during the thermal decomposition of CP-52(a class of CP products).However, the transformation mechanisms of CP-52 to these compounds are still not very clear.This article presents a mechanistic analysis on the decomposition of CP-52 experimentally and theoretically. It was found that CP-52 initially undergoes dehydrochlorination and carbon chain cleavage and it transformed into chlorinated and unsaturated hydrocarbons. Cyclization and aromatization were the most accessible pathways at low temperatures(200–400°C), both of which produce mostly aromatic hydrocarbons. As the temperature exceeds 400°C, the hydrocarbons could decompose into small molecules, and the subsequent radical-induced reactions become the predominant pathways, leading to the formation of Cl-PAHs. The decomposition of CP-52 was investigated by using density functional theory and calculations demonstrating the feasibility and rationality of PCB and PCN formation from chlorobenzene. The results improve the understanding of the transformation processes from CP-52 to SCCPs and Cl-PAHs as well as provide data for reducing their emissions during thermal-related processes.     

Particle number size distribution and new particle formation: New characteristics during the special pollution control period in Beijing

New particle formation is a key process in shaping the size distribution of aerosols in the atmosphere.We present here the measurement results of number and size distribution of aerosol particles (10-1...     

改性氧化铝微波诱导氧化处理雅格素蓝BF-BR染料废水的研究

采用微波诱导氧化工艺(MIOP)技术,以改性氧化铝为催化剂,对雅格素蓝BF-BR染料模拟废水进行氧化处理．优化了处理工艺条件,实验在固液质量比为1：10(50mL雅格素蓝BF-BR水溶液中投加5．0g改性氧化铝)、微波功率为400W的条件下微波辐照处理5min．在此工艺条件下,对水中雅格素蓝BF-BR的脱色率可达到98％,COD去除率为87．4％．改性氧化铝在重复使用9次后仍能保持很高的脱色率．进一步研究表明在微波辐射场中废水中的有机污染物在改性氧化铝表面通过吸附．氧化协同作用而被迅速降解．反应动力学研究表明,该氧化过程符合一级反应动力学规律,反应速率常数k=0995min^-1,反应半衰期t1/2=0．697min．实验结果显示,在本实验中改性氧化铝比颗粒活性炭具有更高的催化活性．