土壤柴油污染修复的抽气提取去除实验研究

为得到土壤气相抽提(SVE)去除柴油的优化条件,进行了一维土柱抽气提取去除柴油污染物的实验研究,研究不同初始含水率、不同抽气量对污染土壤中柴油去除率的影响及不同深度残留柴油的变化规律。结果表明：在本实验模拟的范围内,抽气量越大,SVE处理效果越好;初始含水率越低,处理效果越好;此外,不同深度去除率变化的规律基本上是随深度的增大而减小。实验结果可为土壤轻油污染实际治理提供实验数据基础。     

中国水旱灾害危险性的时空格局研究

水灾与旱灾之间,不论在形成的原因上或是在治理措施上,都存在着相当密切的关系。受季风气候影响,中国的洪水和干旱灾害同时并存,近年来我国遭受极端水旱灾害事件的次数比以往增加很多。基于县域统计单元的水旱灾害信息,以总时段（1949—2005年）、分时段（1956—1965年,1996—2005年）、分季度和分月份4种时间尺度来划分,选取2359个县域单元上的灾害频数作为衡量水旱灾害危险性的指标,主要从危险性整体转移、高危险区转移、转移的形成因素以及高危险区的防灾减灾对策几个角度,探讨了中国水灾、旱灾以及水旱综合灾害的危险性时空分异规律。研究表明：近57年来,中国水旱灾害危险性的整体格局呈现东西分异,东部远远高于西部,这是气候一地貌一人类活动相互作用的产物。1956—1965年,我国水旱灾害危险性格局的东西分异明显;1996—2005年,水旱灾害危险性格局不变,高值区域明显增大,向东北、西北、南方扩展。水旱灾害危险性格局的季节变化显著,整体呈现夏季水旱灾害危险性高,春季次之,秋冬季危险性低的状况;月际变化与降水带的推移和承灾体的月际变化相似,7月水旱灾害危险性达到峰值。上述研究结果可为水旱灾害风险区划以及水旱灾害高危险区的减灾战略规划提供科学依据。     

Modeling VOC-odor exposure risk in livestock buildings

This paper describes a novel idea of linking models of exposure, internal dosimetry, and health effects. Risk assessment approach that integrates predicted odor caused by volatile organic compounds (VOC-odor) of toluene/xylene concentrations in human tissues leads to predict exposure risks in livestock buildings. First, VOC transport model was developed to calculate airborne toluene/xylene concentrations. Based on a physiologically based pharmacokinetic (PBPK) model, concentrations within five compartments representing lung, liver, fat, slowly perfused tissues, and rapidly perfused tissues could be quantified. By using a pharmacodynamic (PD) Hill model, we can optimally fit data from rat and human experiments to reconstruct dose-response relationships for accounting human health effects from nose poke and eye irritation. Results demonstrated that peak tissue concentration occurring at 5-10h in that fat contains the highest concentration than other tissues at around 4ppm of toluene and 1.8ppm of xylene. The EC(10) values are 114 and 232ppm, whereas expected risks are estimated to be 0.71% and 0.26% of human exposure to toluene and xylene, respectively. Risk analyses indicate that inhalation exposure in livestock buildings poses no significant threat to human health under the present environmental conditions. This method provides a rigorous and effective approach to relate target tissue concentration to human nose poke or eye irritation. We suggest that our probabilistic framework and methods be taken seriously because they produce general conclusions that are more robust and could offer a risk-management framework for discussion of future establishment of limits for respiratory exposure to VOC-odor.     

The study on the dechlorination of OCDD with Pd/C catalyst in ethanol-water solution under mild conditions

Dechlorination of octachlorodibenzo-p-dioxin (OCDD) was carried out in ethanol-water (v/v=1:1) solution of NaOH in the presence of Pd/C catalysts with the use of H(2). The substrate was dechlorinated with Pd/C under mild conditions (atmospheric pressure and <100 degrees C) to give a chlorine-free product, dibenzo-p-dioxin (DD), in high yields. After reaction of 3h at 50 degrees C, 95.9% OCDD was degraded to low dechlorinated congeners and the yield of DD was 77.4%. We have also studied the dechlorination selectivity of chlorine atoms on the different substituted positions and postulated the dechlorination pathway of OCDD. For OCDD, the 2-position has higher reactivity than 1-position, but the difference is very small. From the distribution statistics of the intermediates during the reaction, we postulate that the steric effect plays an important role during the reaction and affect the dechlorination pathway of OCDD.     

Decomposition pathways and reaction intermediate formation of the purified, hydrolyzed azo reactive dye C.I. Reactive Red 120 during ozonation

In this study, an aqueous solution of purified, hydrolyzed C.I. Reactive Red 120 (RR 120, Color Index), was selected as a model to investigate the degradation pathways and to obtain additional information on the reaction intermediate formation. The dye was purified to avoid the influence of the impurities on the ozonation process and on the formation of oxidation by-products. To simulate the dye-bath effluents from dyeing processes with azo reactive dyes, a hydrolyzed form of the dye was chosen as a representative compound. High performance liquid chromatography/mass spectrometry and its tandem mass spectrometry was chosen to identify the decomposition pathways and reaction intermediate formation during the ozonation process. In addition total organic carbon and high performance ion chromatography analysis were employed to obtain further information on the reaction processes during ozonation. Purified, hydrolyzed RR 120 was decomposed under the direct nucleophilic attack by ozone resulting in oxidation and cleavage of azo group and aromatic ring, while the triazine group still remained in the solution even after prolonged oxidation time (120 min) due to its high resistance to ozonation. Phenol, 1,2-dihydroxysulfobezene, 1-hydroxysulfonbezene were detected as the degradation intermediates, which were further oxidized by O(3) and *OH to other open-ring products and then eventually led to simple oxalic and formic acid identified by HPIC.     

Determination of Nitrobenzene in Wastewater Using a Hanging Mercury Drop Electrode

The determination of trace amount nitrobenzene in wastewater on a hanging mercury drop electrode was studied. The determination conditions of pH, supporting electrolyte, accumulation potential, accumulation time, and voltammetric response were optimized. The sharp peak of the nitrobenzene was appeared at 0.05 V. The peak electric current was proportional to the concentration of nitrobenzene in the range of 1.47 × 10⁻⁵ ∼ 1.0 × 10⁻³ mol/l with relative standard deviations of 3.99 ∼ 8.94%. The detection limit of the nitrobenzene in water was 5 × 10⁻⁶ mol/l. The proposed method offered low limit of determination, easy operation, the use of simple instrumentation, high sensitivity and good reproducibility. It was applied to the determination of nitrobenzene in wastewater with an average recovery of 94.0% ∼ 105%. The proposed method provided fast, sensitive and sometimes real time detection of nitrobenzene.     

氟里昂12(CCl2F2)燃烧分解催化剂性能的研究

本文对贵金属、氧化物和复合氧化物体系催化剂上氟里昂_(12)(F_(12))燃烧分解反应进行了活性评价和稳定性研究.结果表明:TiO_2,ZrO_2/TiO_2催化剂对氟里昂_(12)燃烧分解反应具有良好的低温催化活性和较好的稳定性,ZrO_2/TiO_2催化剂具有一定的臭氧-催化氧化活性     

贵阳市大气细颗粒物中多环芳烃时空分布特征

对贵阳市不同功能区在不同季节大气PM_(2.5)中多环芳烃(PAHs)进行了采样观测,利用UVD和FLD双检测器串联HPLC法分析了16种优控PAHs。结果显示,在贵阳市主城区PM_(2.5)中PAHs有检出,5个采样点全年ρ(∑PAHs)为4. 44～114 ng/m~3,平均值为24. 96 ng/m~3,其值呈现出夏季最低冬季最高的特征,各个功能区在不同季节ρ(PAHs)不同,大小趋势也不同;四季PAHs单体中均以4-6环为主,占ρ(∑PAHs)的68%以上; PAHs来源解析结果显示,贵阳市大气PM_(2.5)中PAHs来源具有明显的季节特征,春、夏和秋季主要来源是石油燃烧排放,兼有少量的生物质燃烧排放,冬季PAHs主要来源是燃煤和石油燃烧排放。PM_(2.5)中PAHs毒性评价结果表明,贵阳市大气中PAHs的春季、夏季和秋季健康风险较小,冬季健康风险较大。四季各功能区ρ(Ba P)大部分均低于《环境空气质量标准》(GB 3095—2012)规定限值(2. 50 ng/m~3),但冬季除背景点外,其他监测点均超标,最大超标倍数为3. 80倍。     

河流型饮用水水源保护区划分比较

比较分析了国内外河流型水源保护区划分的原则、方法和标准,例证了我国不同省份的划分实践。指出,我国各省多采用经验值划分水源保护区范围,部分省份划分方案久未更新,没有充分发挥保护区的作用。提出,应进一步细化水源保护区划分规范指导要求,及时修订省级水源保护区划分方案,并借鉴国外水源保护区划分经验,通过调整水质标准、重视公众参与、利用地理信息系统等方式划分水源保护区,从源头上预防水源污染,降低饮用水公共风险,保障饮用水安全。     

湘江干流水环境质量演变特征及其关键因素定量识别

为科学有效地保护湘江流域水环境,定量识别湘江干流主要水质指标的驱动因素,该研究基于1990~2016年水质监测数据及沿岸永州 长沙五市社会经济发展指标,采用Mann-Kendall检验法分析湘江干流水环境演变趋势,通过逐步回归分析确定各地区各水质指标主要驱动因素。结果表明：湘江干流COD_Mn、Cd、As整体呈下降趋势,上游BOD₅呈下降趋势,上中游NH₃-N呈上升趋势,中游衡阳、株洲市重金属Cr⁶⁺呈上升趋势,衡阳市TP呈上升趋势,中下游BOD₅呈上升趋势;定量追溯各水质指标影响因素得出工业污染是湘江干流重金属As、Cr⁶⁺、Cd主要驱动因素,永衡株潭地区NH₃-N,衡阳市BOD₅、COD_Mn、TP及衡株潭地区BOD₅均以农业污染影响为主;发现产业结构调整对干流水环境有显著影响,建议在流域产业结构调整过程中加强转型升级。