不同干扰程度下高原湿地纳帕海土壤酶活性与微生物特征研究

采用In-situ野外取样技术与室内实验分析相结合,对不同人为干扰程度下滇西北高原湿地纳帕海土壤酶活性和微生物数量特征进行研究。结果表明：（1）在人为活动干扰下,湿地类型从原生沼泽向沼泽草甸-草甸-垦后湿地逆向演替,F检验显示土壤脲酶、蛋白酶和蔗糖酶活性在各类型湿地间差异显著（F脲酶=14.246,F蛋白酶=13.760,F蔗糖酶=15.392）,表现为垦后湿地〉沼泽草甸〉草甸〉原生沼泽,过氧化氢酶活性差异不显著（F过氧化氢酶=2.697）,且与上述三种水解酶变化规律不同。（2）F检验显示,土壤细菌数量差异显著（F细菌=10.883）,呈现沼泽草甸〉草甸〉垦后湿地〉原生沼泽;土壤真菌与放线菌数量差异显著（F真菌=18.032,F放线菌=15.078）,呈现沼泽草甸〉垦后湿地〉草甸〉原生沼泽。（3）回归分析表明,土壤脲酶与过氧化氢酶极显著正相关。在草甸湿地类型中,土壤脲酶、蔗糖酶、蛋白酶间呈显著线性正相关。土壤酶活性虽与微生物数量相性不显著。（4）纳帕海湿地土壤微生物数量与酶活性变化是对人为不同干扰类型与强度的响应。     

典型地铁站的污染物扩散全尺寸试验研究

为全面了解地铁站内有毒有害气体的扩散发展规律,选取北京某地铁站开展了全尺寸实地扩散试验.利用三维超声波风速仪和多通道风速仪对机械通风工况下的站内流场进行监测,并对其气流组织形式进行分析;采用六氟化硫（SF₆）释放、时序采集和离线检测的方法,研究重气的传输速度和扩散范围等扩散与沉降规律,以期为地铁站内人员疏散路径规划提供数据支撑.结果表明：该地铁站在机械通风工况下,会形成一个较为规律的主流场,将其划分为相对独立的东、西两个区域,污染气体SF₆只能在释放源所处的气流顺向区域内流动,反向区域多个监测点SF₆均未检出;重气在扩散时会出现明显的沉降现象,SF₆浓度由2.5 m处的25 ppm分别升高至1.6 m处的180 ppm和0.5 m处的300ppm,且易于在楼梯、边缘等位置的地面积累从而形成局部高浓度区域,浓度可高达300 ppm以上;少量气体可以通过楼梯进入上层站厅,但浓度总体低于75 ppm,难以进一步由出入口扩散至站外地面;应急处置时,需要尽快将乘客向上层或气流反向区域疏散.     

水相中有机化学品和卤素自由基反应速率常数的定量结构-活性关系模型

卤素自由基尤其是氯自由基在污水中难降解污染物的降解以及表层海水中环境微污染物的降解过程中发挥重要作用,能够影响污染物的环境持久性与毒性风险.在污水及表层海水中存在着多种多样的有机污染物,单纯依靠实验手段测定它们和氯自由基的反应速率常数费时费力并且成本较高.因此本研究通过发展氯自由基与有机污染物的反应速率常数的QSAR模...     

竺山湾流域河湖系统污染物总量控制研究

复杂河湖系统的总量控制需考虑河湖双重控制目标,以太湖西北部竺山湾流域为研究对象,运用排污系数法计算了区域内的入河污染负荷;构建了一维河网和二维湖体水环境数学模型,对水环境数学模型进行了率定;基于多重目标的河网水环境容量计算方法,计算了河网水环境容量,并分配至各控制单元;定量分析了各控制单元各污染物总量达标情况下的削减量及削减率。结果表明:竺山湾流域COD削减量为834.4 t,削减率为13.8%;氨氮削减量为226.1 t,削减率为36.5%;总氮削减量为724.8 t,削减率为55.2%;总磷削减量为108.9 t,削减率为73.4%。论文成果对于开展竺山湾流域污染物总量控制和水环境保护具有重要指导意义,同时为类似的河湖系统水污染物总量控制提供借鉴。     

工业烟气净化系统的风量平衡调节及数值模拟应用研究

为了对某钢铁集团烧结机尾气净化系统的风量平衡进行调节,提出了利用Fluent仿真软件对通风管道内部流场进行数值模拟,在主管和部分支管上设置节流管、调节管径的改进措施。风量模拟结果表明,通风管道的原风量存在严重的不平衡性,吸尘点的风量不平衡率高达75.0%,在部分管道增加节流管可以有效调整管道的风量不平衡性,调整后吸尘点风量的不平衡率为18.8%;对于压力损失较大、风量偏小的管道,可通过管径调节使其风量基本达到设计要求;Fluent仿真软件的风量模拟值与现场实测值有较高的吻合性,数值模拟方法可以为工业烟气净化系统的改造提供参考依据。不仅能够为前期工程设计提供帮助,大大节省工程调试费用,缩短工期,并有助于风量不平衡管道的调节和改造。     

宜兴市城市污水处理厂的水污染特征分析

根据对宜兴市污染源分析,结合当地10座污水处理厂的实际调查,在现阶段排放标准下,利用等标污染负荷法评价出污水厂出水的污染特征;同时,对各污水厂进行污染程度排序,筛选出主要污染源区域及其主要污染物。对比分析表明,污水厂出水一级A标准个别指标超过地表水V类水质标准多倍,其出水入河仍对水环境污染负荷有一定影响;就宜兴污水处理厂而言,等标污染负荷分析表明,宜兴清源污水处理厂为主要污染源,出水污染物中TP和COD为其主要污染物。     

酸浸出法回收冶金污泥中的有价金属

采用二次酸浸出的方法回收镍钴湿法冶金工业污泥中的有价金属。先采用水和硫酸作为浸出剂浸出Mg和Na,最佳工艺条件为浸出液的pH 7.5、浸出时间5 min、浸出剂体积与干污泥质量的比(ω)为10 mL/g。再采用硫酸作为浸出剂、焦亚硫酸钠作为还原剂进行二次酸浸,在硫酸与污泥质量比为1.3、焦亚硫酸钠与污泥质量比为0.3、ω为5 mL/g、浸出温度85℃、浸出时间20 min的最佳工艺条件下,Co、Ni、Cu、Mn和Zn的浸出率分别达92.45%、93.48%、89.52%、97.78%和94.79%。经XRD表征,浸出后污泥中未见原污泥中的矿物相,说明原污泥中的矿物几乎全部被溶解。     

Air pollution and hospital visits for acute upper and lower respiratory infections among children in Ningbo,China: A time-series analysis

Acute upper and lower respiratory infections are main causes of mortality and morbidity in children. Air pollution has been recognized as an important contributor to development and exacerbation of respiratory infections. However, few studies are available in China. In this study, we investigated the short-term effect of air pollution on hospital visits for acute upper and lower respiratory infections among children under 15 years in Ningbo, China. Poisson generalized models were used to estimate the associations between air pollution and hospital visits for acute upper and lower respiratory infections adjusted for temporal, seasonal, and meteorological effects. We found that four pollutants (PM_2.5, PM₁₀, NO₂, and SO₂) were significantly associated with hospital visits for acute upper and lower respiratory infections. The effect estimates for acute upper respiratory infections tended to be higher (PM_2.5 ER = 3.46, 95% CI 2.18, 4.76; PM₁₀ ER = 2.81, 95% CI 1.93, 3.69; NO₂ ER = 11.27, 95% CI 8.70, 13.89; SO₂ ER = 15.17, 95% CI 11.29, 19.19). Significant associations for gaseous pollutants (NO₂ and SO₂) were observed after adjustment for particular matter. Stronger associations were observed among older children and in the cold period. Our study suggested that short-term exposure to outdoor air pollution was associated with hospital visits for acute upper and lower respiratory infections in Ningbo.     

Adsorption of fulvic acid by carbon nanotubes from water

This study investigated adsorption of fulvic acid (FA) by single-walled (SWCNT) and multi-walled carbon nanotubes (MWCNT) and activated carbon. Adsorption of FA depends greatly on the adsorbent surface area and solution pH. SWCNT has higher adsorption than MWCNT and activated carbon. Lower E4/E6 (absorbance at 465 nm to that at 665 nm) and higher E2/E3 (absorbance at 250 nm to that at 365 nm) ratios of the residual FA in solution after adsorption than that of original FA in low pH ranges suggest that aromatic rich FA fractions with polar moieties readily adsorb on the adsorbents. The apparent interaction mechanisms between FA and CNT surfaces include electrostatic, hydrophobic, π-π and hydrogen-bond interactions. FA adsorption was reduced greatly with increasing pH because of the increase of electrostatic repulsion and the decrease of hydrophobic and hydrogen-bond interactions.