Effect of environmental forcing on the fate of nutrients, dissolved organic matter and heavy metals released by a coastal wastewater pipeline

Discharges of nutrients, urea, dissolved organic matter and heavy metals by a sewage underwater pipeline are analysed in comparison to environmental conditions in a shallow coastal zone. Variable thermo-haline stratifications of the water column and currents in upper (2.62-34.97 cm s^-1) and deeper (0.83-10.91 cm s^-1) layers drive vertical diffusion and lateral transport of wastewaters. Loads of reactive phosphorus (0.13 tons d^-1) and ammonium (1.62 tons d^-1) by the pipeline are not negligible compared to the major river loads in the gulf. High concentrations of urea (≤11.51 μmol N dm^-3) were found in the area of wastewater release. Ammonium uptake (6.14-534 nmol N dm^-3 h^-1) strongly exceeded nitrate uptake (0.19-138 nmol N dm^-3 h^-1), indicating that discharges of ammonium by the pipeline are actively assimilated by plankton community even at low levels of light. Distribution of Zn (≤27.7 ppb), Cu (≤25.6 ppb), Cd (≤0.80 ppb) and Pb (≤13.5 ppb) in the water column and the measurement of their complex-forming capacity in seawater did not indicate a persistent perturbation of the pelagic environment due to heavy metals.     

有机物辛醇／水分配系数的计算方法：分子碎片常数法

辛醇／水分配系数是表征有机污染物环境行为的重要参数之一，本文应用于碎片常数计算了１３０余个有机化合物的辛醇／水分配系数对数值，通过计算值与实测值的比较发现，两者之间表现出相当好的一致性，其平均绝对误差为０．１３５，此外，还探讨了该方法应用于不同类型有机污染物时需要注意的问题。     

Differences in nitrous oxide fluxes from red soil under different land uses in mid-subtropical China

Red soil may play an important role in nitrous oxide (N₂O) emissions due to its recent land use change pattern. To predict the land use change effect on N₂O emissions, we examined the relationship between soil N₂O flux and environmental determinants in four different types of land uses in subtropical red soil. During two years of study (January 2005-January 2007), biweekly N₂O fluxes were measured from 09:00 to 11:00 a.m. using static closed chamber method. Objectives were to estimate the seasonal and annual N₂O flux differences from land use change and, reveal the controlling factors of soil N₂O emission by studying the relationship of dissolved organic carbon (DOC), microbial biomass carbon (MBC), water filled pore space (WFPS) and soil temperature with soil N₂O flux. Nitrous oxide fluxes were significantly higher in hot-humid season than in the cool-dry season. Significant differences in soil N₂O fluxes were observed among four land uses; 2.9, 1.9 and 1.7 times increased N₂O emissions were observed after conventional land use conversion from woodland to paddy, orchard and upland, respectively. The mean annual budgets of N₂O emission were 0.71-2.21 kg N₂O-N ha⁻¹ year⁻¹ from four land use types. The differences were partly attributed to increased fertilizer use in agriculture land uses. In all land uses, N₂O fluxes were positively related to soil temperature and DOC accounting for 22-48% and 30-46% of the seasonal N₂O flux variability, respectively. Nitrous oxide fluxes did significantly correlate with WFPS in orchard and upland only. Nitrous oxide fluxes responded positively to MBC in all land use types except orchard which had the lowest WFPS. We conclude that (1) land use conversion from woodland to agriculture land uses leads to increased soil N₂O fluxes, partly due increased fertilizer use, and (2) irrespective of land use, soil N₂O fluxes are under environmental controls, the main variables being soil temperature and DOC, both of which control the supply of nitrification and denitrification substrates.     

天然胶/公共网络/废胶粉互穿聚合物网络

通过互穿聚合物网络技术成功制备了天然橡胶/公共网络/废胶粉共轭三组分,并测定了力学性能和微观形态。结果表明:当A/B摩尔比为2/1、AB含量为4.5%、废胶粉粒径为60目、废胶粉含量为15%时,体系的力学性能最好,共轭三组分天然橡胶/公共网络/废胶粉体系的磨耗体积明显低于两组分天然橡胶/废胶粉体系的磨耗体积。界面共轭互穿改善了界面结合,可减少反复压缩过程中的相间摩擦生热和变形。     

污水处理厂不同工艺的污泥脱水效能分析及其影响因素研究

污泥脱水是污泥减量的主要手段,直接影响到后续污泥处理处置.本研究以北京某大型污水处理厂A2/O工艺和A2/O-MBR工艺污泥脱水为对象,基于2013年全年的运行数据,分析不同工艺的污泥脱水效果、絮凝剂投配率、污泥脱水电耗和污泥脱水成本,并通过冗余分析(RDA)研究了不同污水处理工艺污泥脱水性能的影响因素.结果表明,污泥脱水性能和絮凝剂投配率均呈现季节性变化特征,冬季污泥较难脱水,絮凝剂消耗大.A2/O-MBR工艺的脱水污泥含水率年均值为(81.92±1.64)%,A2/O工艺为(82.56±1.35)%,污泥脱水絮凝剂消耗(以DS计,下同)分别为(8.70±7.25)kg·t-1和(7.42±2.96)kg·t-1,电耗(以DS计,下同)分别为331.82 k W·h·t-1和121.57 k W·h·t-1.A2/O-MBR工艺的污泥脱水絮凝剂成本(以DS计,下同)为204.76元·t-1,用电成本为231.61元·t-1;A2/O工艺的污泥脱水絮凝剂成本为175.00元·t-1,用电成本为84.86元·t-1.RDA分析表明,水温等季节性因素引起污泥有机质变化是影响污泥脱水性能的关键因素之一,此外,污泥龄也与污泥脱水性能有一定相关性.     

长江三角洲地区基于喷涂工艺的溶剂源VOCs排放特征

了解挥发性有机物(volatile organic compounds,VOCs)的溶剂源排放特征是制定长江三角洲地区PM2.5和臭氧防控策略的关键.本研究通过罐采样-GC-MS/FID测定了长江三角洲地区重点喷涂行业(集装箱喷涂、造船喷涂、木器喷涂和汽车喷涂业)的VOCs排放特征.结果表明,长江三角洲地区喷涂行业排放的主要VOCs组分为甲苯、二甲苯、乙苯等芳香烃类物质,三者之和占总VOCs的质量分数为79%~99%.生产工艺的不同对VOCs的排放组成影响并不大,废气处理装置中活性炭吸附对VOCs的组成并无明显影响,而催化燃烧的处理过程会使VOCs的排放组成产生显著变化,乙烯排放明显增大,同时也使得催化燃烧处理最大增量反应活性(maximum increment reactivity,MIR)值高于活性炭吸附处理后的MIR值,说明不同的处理措施的使用将影响VOCs对臭氧的生成作用.     

闽三角城市群自然资本损失评估

在快速城镇化进程中,城市群发展在促进区域经济竞争与合作的同时,也在一定程度上造成人地关系矛盾的加剧,生态系统服务水平下降。为了量化城镇化对自然资本产生的变动,揭示人类资源消耗过程对区域生态系统服务的影响机制,以快速城镇化的典型区域——闽三角城市群为例,运用能值分析方法与GIS技术,分析了2000-2015年闽三角城市群可更新资源时空演变特征,城镇化进程中生态环境价值演变规律以及土地转化过程中的自然资本损失。研究结果表明：（1）闽三角城市群可更新资源在时间上呈波动减小趋势,空间上自沿海区域向内陆区域逐渐升高;（2）高环境质量等级中城镇用地面积占比呈显著增加趋势,由0增加到10.63%,人类活动导致区域生态环境价值的损失逐渐上升;（3）城镇化过程中由于城市空间扩张,使部分自然用地与农业用地转化为城镇用地,转化过程造成的自然资本损失总量为1.27×10²² seJ,货币价值超过6.30×10⁹元。研究有助于完善城镇化影响下的生态环境效应研究,为城市群或区域生态环境管理与修复提供决策参考。     

高有机负荷冲击对填料型MBR运行性能的影响

针对分散式农村生活污水有机负荷变化明显的特点,研究了填料型厌氧-缺氧-好氧膜生物反应器（A²O-MBR）抗高有机负荷的能力,考察了高有机负荷冲击对污染物去除效果、悬浮和附着污泥性质以及膜污染的影响.结果表明,高负荷冲击期间污染物去除稳定,氨氮去除率在冲击第3d从99.1%下降到78.5%,出水氨氮浓度高于5mg/L,随后去除率恢复至97.6%;悬浮和附着微生物的三磷酸腺苷（ATP）含量增加;附着生物量显著增加;细胞外聚合物（EPS）增加;高有机负荷冲击期间膜污染更严重,膜面污染层EPS含量显著增加;太阳能微动力A²O-MBR系统能减少10%的碳排放.     

天然橄榄石对水体铜绿微囊藻的去除效果

为开发安全、高效、廉价的水华控制技术,选择铝土矿、磷铁矿、黄铁矿、铬铁矿及橄榄石等10种天然矿物材料,以水体铜绿微囊藻为研究对象,通过跟踪测定其叶绿素a的变化,研究了天然矿物对水体铜绿微囊藻去除特性,并探讨了天然橄榄石去除铜绿微囊藻的影响因素及去除机理。结果表明：相同条件下天然橄榄石具有最高的除藻能力;矿物用量及藻密度对橄榄石除藻过程影响最大,其次为pH及水温,光强影响最小;当橄榄石浓度为1.5 g·L^‒1,藻密度<1.7×10⁶ cells·mL^‒1、水温15 ℃、反应介质为弱酸性或中性(pH 5~7)时,吸附1 h后,叶绿素a去除率高于96%。进一步分析可知,天然橄榄石主要通过静电作用对铜绿微囊藻进行吸附,进而使藻细胞絮凝沉降,部分藻细胞破裂分解,同时天然橄榄石在反应过程中吸附培养基中的营养盐,造成藻细胞营养缺少,从而对藻细胞的生长造成一定的抑制作用。     

铈负载改性天然沸石催化臭氧氧化水中青霉素G

以改性天然沸石(NZ)为载体,采用等体积浸渍法制备Ce负载天然沸石催化剂(Ce-NZ),将其应用于催化臭氧氧化水中青霉素G(PCN)。比表面积(BET)、扫描电镜-能谱(SEM-EDS)、透射电镜(TEM)和X射线衍射(XRD)表征结果表明,Ce-NZ催化剂保持了天然沸石的表面结构,CeO₂均匀负载在沸石载体的表面。Ce-NZ催化臭氧氧化水中PCN结果显示,催化剂具有良好的活性,在PCN初始浓度为50 mg/L,臭氧投加量为6 mg/min,反应时间为2 h时,4%Ce-NZ催化剂对PCN的去除率为31%,比单独臭氧氧化提高了22%。随着Ce负载量的增加,催化剂的催化活性提高有限,最佳Ce负载量为4%;溶液初始pH对反应有显著影响,提高溶液pH可以提高催化氧化效率;制备的Ce-NZ催化剂稳定性较好,重复使用10次后催化活性没有明显降低。