多层介质水平潜流人工湿地对微塑料的去除研究

以具有相同结构的两个多层介质水平潜流人工湿地为研究对象,考察了湿地单元进水、出水和植物根系附近的微塑料丰度、物理尺寸变化特征,并分析了湿地内部植物根系、湿地生物系统、悬浮物等去除微塑料的机理。结果表明,近年来在河道水质提升工程中常使用的较大粒径多层介质人工湿地能够有效降低天然河流水体中的微塑料丰度。在连续7 d的监测中,两个湿地单元对微塑料的平均去除率分别为26.91%和27.00%,最高分别达到了44.83%和44.59%。湿地单元对400～<800μm的微塑料去除率在20%～50%,而对800～<1 200μm和≥1 200μm的较大尺寸微塑料去除率可达到50%以上。湿地单元前部的植物根系对微塑料具有更明显的截留作用,且对≥800μm的较大尺寸微塑料截留效率更佳。人工湿地去除微塑料的效率可能与微塑料形状、湿地植物、水流速度、内部填料粒径及生物膜生长状况等多种因素有关。     

生物质碳源组合型生态浮床系统脱氮效果研究

利用农业废弃物和水生植物,结合水下空间与水面景观,构建集成脱氮技术的新型立体组合式生态浮床系统用以地表水体中氮的脱除以净化水质。立体生态浮床运行2个月之后的结果显示,NH3-N、TN和CODMn的去除率可分别达到96.77%、95.51%和77.75%,本浮床具有较高脱氮能力,水体净化效果明显;同时,整个生态浮床系统的生物多样性较为丰富,原水分别为Ⅴ类和劣Ⅴ类的池2和池5中分别鉴定出6种和8种主要氨氧化菌谱带,位于系统中部的玉米芯和稻草表面微生物多样性丰富程度较高;稻草和底泥中氨氧化菌的谱带种类最多。与池2相比,池5中除了存在共有谱带外,还存在特有谱带h和j带,表明可能有特殊氨氧化菌群的存在。本组合型生态浮床具有同步硝化与反硝化作用,利于沉水植物生长,并能促进水生态系统构建。     

植物群落对湿地净化生活污水的影响

为解决植物配置对水质净化影响问题,研究了不同植物群落对生活污水的净化效果及其响应机理,并探索了人工湿地植物的最佳组合.结合景观生态学,运用7种湿地植物构建4种植物群落的人工湿地CW-G1、CW-G2、CW-G3、CW-G4,HRT为4d,水力负荷为0.125 m3.(m2.d)-1,分析了各人工湿地对污染物的去除率,通...     

模拟垂直潜流人工湿地中植物种类和植物多样性对脱氮效果的影响

在模拟垂直潜流人工湿地中选种了水烛和菩提子两种常见湿地植物,以氨氮为湿地唯一氮源,通过植物单种和混种研究了植物种类和植物多样性对湿地脱氮效果的影响。结果表明,菩提子单种时,出水氮浓度均明显低于水烛单种。菩提子单种时,出水硝态氮、氨氮、总无机氮(TIN)质量浓度分别为72.34、13.80、86.14mg/L;水烛单种时,出水硝态氮、氨氮、TIN质量浓度分别为235.41、32.12、267.53mg/L。水烛与菩提子混种时,出水比菩提子或水烛单种具有更低的硝态氮和TIN,硝态氮和TIN质量浓度分别为55.60、80.50mg/L。因此,相比水烛,菩提子更有利于湿地脱氮;加强植物多样性可提高湿地的脱氮效果。湿地的脱氮效果与植物生物量具有显著相关性。     

种植不同植物的表面流人工湿地净化效果和微生物群落差异分析

为了解植物种类对表面流人工湿地的净化效果的影响及其与微生物群落的关系,研究了4种植物条件下表面流人工湿地的氮磷平衡以及微生物群落结构。结果表明,各组人工湿地对氨氮(45.53%～80.95%)、总氮(53.67%～80.30%)和总磷(32.97%～55.77%)都有较好的处理效果,种植植物的人工湿地比未种植的人工湿地具有更高的氨氮、总氮和总磷去除效果,其中黄菖蒲组对氮的去除效果最好,美人蕉组对磷的去除效果最好。在表面流人工湿地中,微生物作用(34.84%～45.44%)是人工湿地氮去除的主要途径,基质吸附(20.90%～23.91%)是人工湿地磷去除的主要途径,但是种植植物的人工湿地的氮磷通过微生物去除的量更高。高通量测序分析表明,相较于未种植植物的人工湿地,种植植物的人工湿地显示出更高的微生物丰富度、多样性和更高的脱氮除磷功能微生物的丰度。假单胞菌属、不动杆菌属、芽孢杆菌属和硝化螺菌属是人工湿地中主要的脱氮菌属,也是种植植物的人工湿地高生物脱氮的原因。假单胞菌属和不动杆菌属丰度增加是种植植物的人工湿地高生物除磷的原因。     

冬季生态浮床对浮游藻类数量及生物多样性的影响

为了考察生态浮床在冬季的运行效果,选择世博园区白莲泾生态浮床工程为研究对象,研究了冬季生态浮床对浮游藻类数量及生物多样性的影响。结果表明,取样期间浮游藻类生物总量逐月增加,且对照区明显高于浮床区;浮床区与对照区浮游藻类的种群结构差异明显,浮床区以硅藻门为主,而对照区以绿藻门为主。并且,小环藻与细微颤藻的优势度指数均有明显的下降。同时,浮床区的Shannon-Wiener多样性指数明显高于对照区。以上结果均证明,虽然在冬季较低温的情况下水生植物新陈代谢缓慢,但生态浮床仍会影响浮游藻类的数量及生物多样性,从而对水质净化起到一定的改善作用。     

滨河湿地对农业非点源氮污染控制研究进展

氮素是农业径流最重要、最普遍的水体污染物。滨河湿地因受到陆地生境和水生生境双重影响而显得非常独特,作为重要的陆地和水生环境的生态交错带,滨河湿地能够阻断和改变水运污染物,特别是农业径流中的氮排入临近的小溪和河流。植物吸收和反硝化作用是滨河湿地两种最重要的截留和缓解氮负荷的有效途径,氮素可以通过生物转化、植物吸收、微生物暂时固氮等方式去除,但是永久性的去除氮却是通过反硝化过程来完成的。为了系统认识和了解滨河湿地生态系统对农业非点源氮污染控制过程,通过大量文献分析讨论了滨河湿地对农业非点源氮的净化能力、净化机制及其影响因素,并结合我国研究现状展望了该领域的研究前景。滨河湿地对农业非点源氮污染的控制作用研究将成为滨河湿地生态系统服务功能评价、滨河湿地生态系统健康与稳定的诊断和退化滨河湿地生态系统修复的重要基础理论。     

不同粒径生物炭和泥鳅对人工湿地植物根系形态及基质硝化与反硝化能力的影响

向人工湿地中加入2种粒径(粒径1~2 mm和粒径1 mm)生物炭和泥鳅,研究了不同粒径生物炭和泥鳅对湿地植物根系形态和基质硝化与反硝化强度的影响。结果表明,向人工湿地中加入泥鳅和生物炭,降低了基质的氨态氮含量,增加基质的硝态氮含量、硝化强度和反硝化强度;与粒径小(1 mm)的生物炭相比,添加粒径大(1~2 mm)的生物炭后,湿地基质的氨态氮含量、硝态氮含量和反硝化强度分别降低了46.6%、51.1%和35.4%。加入生物炭和泥鳅均增加了湿地植物总根长和总根体积,然而与粒径小的生物炭相比,添加粒径大的生物炭后,人工湿地中植物总根长和总根体积分别降低了15.1%和6.8%。基质硝态氮含量与人工湿地中植物总根长和总根体积分别呈显著相关关系(α=0.01)。结果表明,生物炭提高了人工湿地基质硝化强度,有利于硝态氮的生成,促进人工湿地中植物根的生长,增加了总根长和总根体积。     

进水碳负荷浓度对垂直潜流式人工湿地中植物根系微生物动态的影响

植物的不同生长发育阶段是影响根系微生物功能多样性的原因之一。植物的生长改变了微生物的群落结构。在低有机负荷或高有机负荷下,植物幼苗与成苗根系的微生物整体活性均差异明显,一般成苗期具有较高AWCD值。有植物湿地中微生物Simpson和Mcintosh多样性指数在植物成苗期均明显高于幼苗期(P0.05),但Shannon指数变化不明显(P0.05)。无植物湿地中微生物Simpson和Mcintosh指数受季节影响差异显著(P0.05)。主成分和聚类分析结果表明,不同生长发育阶段其微生物种类存在差异,而且不同进水条件下有植物湿地和无植物湿地各自有相似的微生物群体结构。     

植物配置对表层流湿地净化效果的影响研究

以郑州市贾鲁河河水为处理对象,研究了不同植物配置表层流湿地的水质净化效果及影响因素。研究表明,单纯挺水植物湿地对TN、TP、NH4+-N和COD的平均去除率分别为28%、58%、49%和26%;采用沉水植物+浮叶植物+挺水植物组合的湿地对TN、TP、NH4+-N和COD的平均去除率分别为37%、64%、63%和32%,在对NH4+-N和TN的处理效果上表现出明显的优势,DO含量变化是导致处理效果差异的主要原因。研究结果表明,在湿地植物配置上,可从氮循环的角度,通过合理搭配湿地植物,强化硝化反硝化作用,以提高对氮素的去除效果。     

An application of the theory of kinematics of mixing to the study of tropospheric dispersion

The most common technique used for numerical simulations of tracer mixing is that of the numerical solution of the advection–diffusion equation with the unresolved fluxes parameterized using the similarity theory. Despite correct predictions of the overall directions of transport, models based on a numerical solution of the advection–diffusion equation lack sufficient accuracy to correctly reproduce the coupling of mixing with small scale processes which are sensitive to the microstructure of the tracer distribution. The objective of this paper is to revisit the basic formalism employed in numerical models used to investigate atmospheric tracers. The main mathematical method proposed here is the theory of kinematics of mixing which could be applied effectively for simulations of atmospheric transport processes. At the beginning of the paper, we introduce simple mathematical transformations in order to demonstrate how complex topological structures are created by mixing processes. These idealistic flow systems are essential to explain transport properties of much more complex three-dimensional geophysical flows. An example of the application of the kinematics of mixing to the analysis of tracer transport on a planetary scale is presented in the following sections. The complex filamentary structures simulated in the numerical experiment are evaluated using some commonly applied statistical measures in order to compare the results with the data published in the literature. The results of the experiment are also analysed with the help of simple conceptual models of fluid filaments. The microstructure of the tracer distribution introduced in the paper is essential to increase our understanding of atmospheric transport and to develop more realistic parameterizations of small-scale mixing. The presented results could also be used to improve calculations of the coupling between microphysical processes and tracer mixing.     

Estimation of uncertainty of sampling for analysis of pesticide residues

Abstract

A computer model was used to take random samples from primary sample populations obtained from field trials to simulate the uncertainty of sampling for residue analysis of plant commodities and soil. The results indicate about 40%, 30% and 20% relative uncertainty when random samples of size 5, 10 and 25 are taken respectively, from a single lot. Therefore the sample size should be the same for establishing and enforcing legal limits.     

次氯酸钠发生器的研制

介绍了电解法生产次氯酸钠的原理 ,并在原有生产工艺的基础上进行了重新设计和对设备的重新选择、改造 ,得出了各个工艺参数的最佳值 ,生产出高品质的次氯酸钠     

生物质快速热裂解主要参数对生物油产率的影响

以松木木屑为原料,在自制的小型流化床上,开展了生物质热裂解温度、生物质粒径和进料速率对生物油产率的影响实验研究.结果表明,在热裂解温度分别为450、475、500、525和550℃条件下,当热裂解温度为500℃时,生物油产率最高,平均产率达到53.33%(质量百分比).反应温度越高,炭产量越低,不可冷凝气体产量越高,气体发热值越高;粒径＜1 mm的生物质其粒径对生物油产率影响不大;生物质进料速率增加时,生物油产率增加.本研究为生物能的利用提供了新的途径.     

不同泥源对厌氧氨氧化反应器启动的影响

采用2套上流式生物膜反应器,分别接种少量厌氧氨氧化污泥和大量硝化污泥,考察其对厌氧氨氧化反应器启动的影响。污泥接种入反应器后,测得接种厌氧氨氧化污泥的反应器(R1)内MLSS为0.22 g/L,另一个反应器(R2)MLSS为2.7 g/L。与直接接种厌氧氨氧化污泥相比,R1经过72 d的运行才显现出厌氧氨氧化特性。经过114 d的培养,前者氮去除速率由0.23 kg/(m3.d)提升到5.29 kg/(m3.d),总氮去除率大于89%;R2的氮去除速率由0.01 kg/(m3.d)提升到1.1 kg/(m3.d),总氮去除率大于84.6%。说明普通污泥启动需要一个较长的筛选过程,直接接种少量的厌氧氨氧化污泥比接种普通的污泥能够更快启动厌氧氨氧化反应器。     

Visualisation of the complexity of EUSES

The interdependencies of parameters applied in the models of EUSES are visualised in a directed connectivity graph. The parameters (inputs, defaults, state variables, outputs) are represented by boxes (nodes) and their relations by lines (edges). The visualisation, on the one hand, clarifies the complexity of the models in EUSES and, on the other hand, creates an overview and transparency. The parameters’ relations to each other can be recognised faster, and the models can be better understood. The complexity was quantified by the number (variety), kind (substance parameter, physico-chemical parameter, concentration, other parameters), and depth (dimension) of the parameter and the number of relations (connectivity). The variety of EUSES (without the modelsSimple Treat andSimple Box whose interior structure is not documented and without the effect and risk characterisation) amounts to 466, the connectivity to 961, and the maximal dimension is 21.     

造纸废水混凝处理中SFT助凝替代性研究

中小造纸厂废水处理常用PAC作混凝剂 ,PAM作助凝剂。由于PAM成本很高 ,影响了处理设备的投运率。用超细滑石粉 (SFT)替代PAM助凝 ,与混凝剂PAC配合 ,其混凝处理效果基本相当 ,但是处理成本降低 0 .10元 /m3 。由于SFT属环境无害材料 ,不会给排泥带来二次污染     

Evaluation of the presence of drugs of abuse in tap waters

A total of seventy samples of drinking water were tested for non-controlled and illicit drugs. Of these, 43 were from Spanish cities, 15 from seven other European countries, three from Japan and nine from seven different Latin American countries. The most frequently detected compounds were caffeine, nicotine, cotinine, cocaine and its metabolite benzoylecgonine, methadone and its metabolite EDDP. The mean concentrations of non-controlled drugs were: for caffeine 50 and 19 ng L⁻¹, in Spanish and worldwide drinking water respectively and for nicotine 13 and 19 ng L⁻¹. Illicit drugs were sparsely present and usually at ultratrace level (<1 ng L⁻¹). For example, cocaine has mean values of 0.4 (Spain) and 0.3 ng L⁻¹ (worldwide), whereas for benzoylecgonine, these mean values were 0.4 and 1.8 ng L⁻¹, respectively. Higher concentrations of benzoylecgonine were found in Latin American samples (up to 15 ng L⁻¹). No opiates were identified in any sample but the presence of methadone and EDDP was frequently detected. Total mean values for EDDP were 0.4 ng L⁻¹ (Spain) and 0.3 ng L⁻¹ (worldwide). Very few samples tested positive for amphetamines, in line with the reactivity of chlorine with these compounds. No cannabinoids, LSD, ketamine, fentanyl and PCP were detected.     

产油微藻培养与回收的关键技术研究进展

寻找廉价而高效的替代原料是实现生物柴油产业化的关键所在.微藻以含油量高、生长周期短、环境适应能力强、生物产量高等优点,有望成为一种极具潜力的生物柴油生产原料.然而,目前尚存在微藻培养低效成本高和微藻回收效率低两大难题.综述了微藻培养与回收过程中的关键技术,并对存在的两大难题及其改进技术进行了详细的探讨.最后,总结并展望了微藻培养、回收技术未来的发展趋势.     

Mechanisms of biodegradation of dibenzoate plasticizers

Biodegradation mechanisms were elucidated for three dibenzoate plasticizers: diethylene glycol dibenzoate (D(EG)DB), dipropylene glycol dibenzoate (D(PG)DB), both of which are commercially available, and 1,6-hexanediol dibenzoate, a potential green plasticizer. Degradation studies were done using Rhodococcus rhodochrous in the presence of pure alkanes as a co-substrate. As expected, the first degradation step for all of these systems was the hydrolysis of one ester bond with the release of benzoic acid and a monoester. Subsequent biodegradation of the monobenzoates of diethylene glycol (D(EG)MB) and dipropylene glycol (D(PG)MB) was very slow, leading to significant accumulation of these monoesters. In contrast, 1,6-hexanediol monobenzoate was quickly degraded and characterization of the metabolites indicated that the biodegradation proceeded by way of the oxidation of the alcohol group to generate 6-(benzoyloxy) hexanoic acid followed by β-oxidation steps. This pathway was blocked for D(EG)MB and D(PG)MB by the presence of an ether function.The use of a pure hydrocarbon as a co-substrate resulted in the formation of another class of metabolites; namely the esters of the alcohols formed by the oxidation of the alkanes and the benzoic acid released by hydrolysis of the original diesters. These metabolites were biodegraded without the accumulation of any intermediates.