Enhanced biological nutrient removal by the alliance of a heterotrophic nitrifying strain with a nitrogen removing ecosystem

Nitrogen removal from synthetic wastewater was investigated in an airlift bioreactor （ALB）, augmented with a novel heterotrophic nitrifier Pseudonocardia ammonioxydans H9^T under organic carbon to nitrogen ratios （Corg/N） ranging from 0 to 12. Effect of the inoculated strain was also determined on the settling properties and the removal of chemical oxygen demand （COD）. Two laboratory scale reactors were set up to achieve a stable nitrifying state under the same physicochemical conditions of hydraulic retention time （HRT）, temperature, pH and dissolved oxygen （DO）, and operated under the sequencing batch mode. The level of DO was kept at 0.5- 1.5 mg/L by periodic stirring and aeration. Each specific Corg/N ratio was continued for duration of 3 weeks. One of the reactors （BR2） was inoculated with P ammonioxydans H9^T periodically at the start of each Corg/N ratio. Sludge volumetric index （SVI） improved with the increasing Corg/N ratio, but no significant difference was detected between the two reactors. BR2 showed higher levels of nitrogen removal with the increasing heterotrophic conditions, and the ammonia removal reached to the level of 82%-88%, up to10% higher than that in the control reactor （BR1） at Corg/N ratios higher than 6; however, the ammonia removal level in experimental reactor was up to 8% lower than that in control reactor at Corg/N ratios lower than 2. The COD removal efficiency progressively increased with the increasing Corg/N ratios in both of the reactors. The COD removal percentage up to peak values of 88%-94% in BR2, up to 11% higher than that in BR1 at Corg/N ratio higher than 4. The peak values of ammonia and COD removal almost coincided with the highest number （18%-27% to total bacterial number） of the exogenous bacterium in the BR2, detected as colony forming units （CFU）. Furthermore, the removal of ammonia and COD in BR2 was closely related to the number of the inoculated strain with a coefficient index （R2） up to 0.82 and 0.85 for ammonia and     

Zn/Fe体系湿法催化氧化高效脱除沼气中H2S的研究

提出了Zn/Fe体系湿法催化氧化脱除沼气中H2S新工艺,阐述了反应机理、实验装置和工艺流程,考察了各单因素操作条件对H2S脱除效率的影响,在此基础上进行的综合条件实验,脱硫效率都维持在99.6%以上,净化后沼气中H2S含量低于国家标准。过程不消耗任何化工原料,不产生二次污染,体系无降解问题。     

水质总磷总氮在线自动监测技术的研究

通过优化国内外水质总氮总磷的手工和自动监测方法及设计参数,研究了基于紫外催化-过硫酸钾氧化分光光度法的在线监测技术,设计了紫外线加强氧化-消解反应器和20通道自动校准与自动进样集成控制系统。该技术与国家标准监测方法相比大大提高了总磷总氮氧化率和消解速度,实现了在较低温度和常压条件下水质总磷总氮的快速、安全和稳定的在线自动监测,具备了良好的市场推广应用前景。     

基于土壤流失的农业面源TN和TP排海系数估算

以黄河三角洲为典型研究区,通过分析区域地表污染物流失风险与入海通量的关系,构建了海岸带农业总氮（TN）和总磷（TP）面源污染排海估算模型.在此基础上,计算了包含水田、水浇地和旱地等耕地类的TN和TP面源污染排海系数,验证表明输出系数估算结果较好.研究区耕地的TN和TP排海系数分别为18.33 kg·（hm²·a）^-1和1.02 kg·（hm²·a）^-1,在夏季面源污染负荷较高.子流域尺度较大的耕地类农业面源污染负荷主要位于支脉河、广利河和小岛河管控区域.TN和TP总负荷较大的行政区主要位于北部黄河口镇和永安镇;较大的单位面积负荷在西南部.因此,需要关注农业面源污染的时间效应,同时协调社会经济发展,从子流域和行政单元的角度制定综合性面源污染防控策略,陆海统筹治理海域污染.     

长柄石杉居群遗传多样性和遗传结构的AFLP分析

石杉科植物因所含石杉碱甲(Huperzine A)对中老年痴呆等具有良好疗效,近年来倍受关注.利用AFLP分子标记对武夷山脉广布种长柄石杉[Huperzia serrata(Thunb.ex Murray)Trev.var.longipetiolata(Spring)H.M.Chang]7个居群112株个体进行遗传多样性和居群遗传结构分析.选用多态性高、分辨力强的8对选择性扩增引物组合共获得675个位点,其中多态位点比例为69.38%.居群内观测等位基因数(Na)为1.633,有效等位基因数(Ne)1.493;Nei’s基因多样性指数(He)与Shannon多态性信息指数(I)的平均值分别为0.272和0.392,多样性最高为地处武夷山脉中段的泰宁居群和建宁居群,最低为山脉北段的光泽居群.居群总基因多样性(Ht)为0.327 3,居群内基因多样性(Hs)为0.272 2,居群间的遗传分化系数(Gst)为0.168 1,表明居群内变异是长柄石杉遗传多样性的主要来源.由Gst估计,武夷山脉长柄石杉自然居群的基因流(Nm)为2.474 0.邻接树分析表明居群间遗传亲缘关系与地理位置相关.武夷山脉长柄石杉较高的遗传多样性和基因流水平表明其仍然具有相当的适应(生存)能力和进化潜力,这可能与其生物学(异交水平)、生态学特性及武夷山脉相对良好的生境条件有关.     

小流域面源污染减控措施优化管理

以长春市重要饮用水源地石头口门水库的莫家沟小流域为研究区,选择横垄耕作、修建梯田、退耕还林、化肥减施和人工湿地5种措施进行磷素削减处理,共计21个措施组合方案;以实施措施的费用最小为目标函数,以水库水质TP浓度和采用不同措施的土地面积为约束条件,建立小流域出口水质优化管理模型。模拟计算3个阶段的可行性最优方案分别为:2011—2020年,选取措施为施肥量不变,现状梯田面积不变,坡度≤5°的耕地采取横垄耕作,其他退耕还林;2021—2030年,在第一阶段实施方案的基础上,新建人工湿地0.03 km2;2031—2050年,全部农田原位退耕还林,保持人工湿地面积不变,最终实现入库水质ρ(TP)≤0.01 mg.L-1的目标。化肥减施和梯田建设面积是影响方案选择的主要因素。     

油罐喷射火燃烧模拟

针对由一定压力的单相或两相介质泄漏或压力泄放系统排放引起的喷射火,利用gambit生成计算区域网格,得到相应的计算模型.再利用Fluent软件中的离散相模型计算气体流动,采用Realizable k-epsilon湍流模型和部分预混燃烧模型来预测燃料的燃烧,模拟了戊烷燃料燃烧和湍动多相流场,给出了燃烧速度矢量、温度和组...     

Co-pyrolysis of oil sludge with hydrogen-rich plastics in a vertical stirring reactor: Kinetic analysis,emissions, and products

● Collaborative treatment of plastics and OS was established to improve oil quality. ● PE addition successfully improved OS pyrolysis process by deploying H/C_eff ratio. ● Higher H/C_eff ratio promoted cracking to obtain more gas and light oil fractions. ● The degradation of PE and OS was promoted each other under their temperature range. Pyrolysis is an effective method to treat oily sludge (OS) due to its balance between oil recovery and nonhazardous disposal. However, tank bottom OS contains a high content of heavy fractions, which creates obstacles for pyrolysis due to the high activation energy. The incomplete cracking of macromolecules and secondary polymerization decreases the oil quality and causes coking during the operation process. This study introduced polyethylene (PE) into OS to deploy the H/C_eff ratio of feedstocks for pyrolysis. A strong interaction between OS and PE during copyrolysis could be observed from the TG/DTG curves. PE tightly participated in OS degradation, while OS also promoted PE degradation at high temperature. Apparent pits were generated in solid residues from copyrolysis, which was attributed to the uniform and violent gas release. In addition to HCN, other nitrogenous and sulphurous pollutants were inhibited. Accordingly, more gas products were attained after PE addition with more value-added compositions of alkanes and alkenes. Although the oil yield decreased after PE addition, the oil products from copyrolysis possessed higher heating values and higher contents of light fractions with short chains as well as paraffins. Consequently, copyrolysis of OS and PE significantly improved the pyrolysis process and resulted in high oil quality.     

电化学间接氧化法处理H2S气体的研究

采用填料塔对铁盐溶液吸收H2S 的过程进行了初步研究,考察了气液比、填料层高度、吸收温度、Fe^3 浓度,进气H2S浓度和H^ 浓度等因素对H2S去除率的影响。结果表明,气液比、 填料层高度和吸收温度对吸收效率的影响比较显著。通过正交试验选出最佳工艺条件,在此工艺条件下H2S的去除率 接近100％。     

H-酸的催化湿式氧化反应过程研究

湿式氧化（ＷＡＯ）和催化湿式氧化（ＣＷＡＯ）都能有效地处理染料中间体－－Ｈ－酸。所有的Ｈ－酸在５ｍｉｎ内均被支除和形成一些中间产物。在不同反应时间段测定了ｐＨ值及阴、阳离子和小分子有机酸等中间产物。分析表明,ｐＨ值与ＣＯＤ的去除及有机酸的产生有密切的联系,Ｈ－酸被氧化成ＮＨ４＾＋、ＳＯ４＾２－、ＨＣＯＯＨ和ＣＨ２ＣＯＯＨ。ＷＡＯ法的瓜速率慢而且氧化乙酸困难。而ＣＷＡＯ法的反应速率不但快而且能有效地