共查询到18条相似文献，搜索用时 171 毫秒
1.
东巢湖沉积物水界面氮、磷、氧迁移特征及意义 总被引：2，自引：0，他引：2
以东巢湖近城市湖湾沉积物为研究对象,在沉积物氮、磷营养盐分析的基础上,采用沉积物柱状芯样静态释放模拟法定量评估研究区域沉积物—水界面氨氮、溶解性活性磷酸盐营养盐释放潜力,利用微电极非损伤测定技术获得沉积物—水微界面溶解氧(DO)剖面分布及微界面DO消耗和扩散特征.结果表明:东巢湖近城市湖湾沉积物氮、磷污染物蓄积量较高,受TN、TP污染程度较重.沉积物内源氨氮、磷酸盐释放明显,平均释放速率分别达到32.44 mg/(m~2·d)和1.25mg/(m~2·d),区域内沉积物已成为水柱中氮、磷营养盐的污染源.研究区域上覆水体处于好氧状态,沉积物—水微界面平均DO穿透深度(OPD)达到5.3 mm,平均DO扩散通量为4.56 mmol/(m~2·d),表现出良好的DO扩散能力.沉积物内源氨氮和磷酸盐释放能力与表层沉积物TN/TP物质含量及沉积物—水微界面DO穿透深度有关,在沉积物氮、磷污染较重的情况下,DO穿透深度越低越有利于氮、磷污染物从沉积物向上覆水体释放. 相似文献
2.
为研究黑臭河道沉积物资源化利用方式，评估沉积物资源化以后对营养盐去除效果和研究其去除机制，以北京市某黑臭河道沉积物（S）为供试样品，对其进行氧化并负载金属离子改性，最终得到氧化-载钠改性沉积物（MS）.选取S和MS两种材料，评估其对氮和磷的去除效果，通过采用动力学、热力学等手段，进一步阐明改性材料对氮、磷去除机制.结果表明，在环境温度为35℃，固液比1：50（g：ml）的条件下，经氧化-载钠联合改性材料对氮（初始浓度20 mg/L）的去除效果均达到90%以上，其中对磷（初始浓度10 mg/L）的去除率最高可达98%；准二级动力学模型能更好的描述改性材料的吸附动力学行为（R2>0.93），且动力学和吸附等温分析结果显示，Langmuir模型可以更好地描述两种材料的吸附等温线，改性材料对氮和磷的最大吸附量分别达到0.891和0.474 mg/g；热力学研究结果表明，吸附过程中，标准反应焓变（ΔH0）、标准反应熵变（ΔS0）均为正值，标准吉布斯自由能变（ΔG0）为负值，且随着温度的升高，ΔG0呈下降趋势.研究显示，MS具有更高的吸附性能，对氮、磷的吸附主要是材料表面活性吸附点位起主导作用，并且吸附过程是个吸热、自发进行的过程，更高的温度更有利于吸附.在同一温度下，随着氮、磷初始浓度的增加，MS对氮、磷的解吸比吸附过程更容易发生. 相似文献
3.
为研究滇池内源污染特征,2013年利用GIS软件针对滇池全湖布设36个采样点,采集表层沉积物,研究滇池表层沉积物铵态氮(NH_4+-N)吸附特征,同时分析沉积物的理化性质对NH_4+-N吸附特性的影响.结果表明:滇池表层沉积物对NH_4+-N的吸附量在前2 h之内呈增长趋势,吸附速率较大,之后沉积物对NH_4+-N的吸附量不随时间变化而变化,基本达到平衡,最大吸附速率均发生在0~5 min内;不同区域表层沉积物NH_4+-N最大吸附速率平均值表现为:外海南部湖心区外海北部草海,最大吸附量平均值表现为:湖心区外海南部外海北部草海,吸附效率平均值表现为:外海北部草海湖心区外海南部;沉积物对NH4+-N的吸附量与NH_4+-N的初始浓度大致呈线性关系,并且低浓度下表现出很好的吸附/解吸特征;滇池表层沉积物NH_4+-N的吸附解吸平衡浓度(ENC0)高于上覆水中NH_4+-N浓度,表明沉积物中NH_4+-N有向上覆水中释放的风险,沉积物在很长一段时间内起到水体污染"源"的作用;ENC0与沉积物中总氮、NH_4+-N含量呈显著正相关,本底吸附量和有机质总量呈显著负相关,沉积物吸附NH_4+-N主要受有机质的影响. 相似文献
4.
过氧化钙对水中低浓度磷的去除性能 总被引：1，自引：0，他引：1
针对水体中低浓度磷深度净化问题,以过氧化钙为吸附剂,采用等温吸附、吸附热力学模型和吸附动力学模型的方法开展其对磷酸盐吸附特性的研究,讨论p H、共存阴离子对其除磷过程的干扰能力.结果表明:(1)过氧化钙对磷酸盐的吸附等温线方程符合Langmuir方程,过氧化钙对磷酸盐的最大吸附量为381.7 mg/g(25℃);(2)过氧化钙在除磷过程中系统的热力学参数ΔG00,ΔH00,即过氧化钙对磷的吸附作用是一个自发的放热过程;(3)二级反应速率方程可精准地描述过氧化钙的吸附行为,其吸附速率随着溶液中磷酸盐浓度的升高而升高,经过4 min即可达到吸附平衡;(4)过氧化钙在p H=8时除磷效果达到最佳;(5)高浓度倍数的共存阴离子中,CO2-3对过氧化钙除磷影响最大,在10倍浓度下可造成吸附量减少14.7%. 相似文献
5.
有机质对城市污染河道沉积物铵态氮吸附-解吸的影响 总被引：2，自引：0，他引：2
采集污染程度不同的城市河道沉积物(通吕运河、濠河和通甲河),在分析H2O2对沉积物有机质和铵态氮影响的基础上,分析沉积物在去除有机质前后铵态氮释放动力学和吸附热力学过程,研究城市污染河道沉积物有机质对铵态氮吸附-解吸的影响.结果表明:单位体积H2O2对有机质去除率随H2O2使用量增多而降低;去除有机质后,沉积物铵态氮含量显著增加,通吕运河、濠河和通甲河铵态氮最大含量分别是有机质去除前的4.16、3.55和2.85倍;沉积物对铵态氮的饱和吸附量随有机质含量减少而下降;沉积物铵态氮释放过程均表现为先快速释放,后减缓至平衡过程;去除有机质后,随着有机质含量的减少,沉积物铵态氮的最大释放量呈增大趋势;沉积物有机质和铵态氮含量是影响沉积物铵态氮释放的主要因素. 相似文献
6.
太湖表层沉积物磷的吸附容量及其释放风险评估 总被引：34，自引：2，他引：34
利用沉积物磷吸附指数(PSI)和磷吸附饱和度(DIS)等指标来表征太湖表层沉积物的磷吸附容量，并探讨了太湖沉积物磷吸附容量的空间变化．研究发现：草酸铵提取的磷以及活性铁、铝氧化物含量在梅梁湾东北部至五里湖一带的沉积物中较高，而在太湖南部湖区相对较低，这主要是与附近城市污水的实际贡献有着密切关系；太湖沉积物的磷吸附指数大体上有着北高南低、西高东低的分布特征，而磷吸附饱和度分布与PSI恰有相反的特征；沉积物中磷的吸附容量可能主要受到无定形的铁和铝的氧化物控制，也受沉积物有机质含量的影响．初步确定了用磷吸附指数和磷吸附饱和度来表征的湖泊沉积物磷释放风险指数概念，并应用于对太湖沉积物磷诱发的富营养化风险的评估． 相似文献
7.
白洋淀沉积物氮磷赋存特征及其内源负荷 总被引：11，自引：2，他引：9
白洋淀环境整治对区域生态文明建设具有重要意义，然而，目前对加剧白洋淀富营养化的内源氮、磷污染负荷依然缺乏系统的研究.本研究以野外调研和室内培养实验相结合形式，在白洋淀主要水域内采集原位柱状沉积物样品，详细地研究了白洋淀沉积物中氮、磷赋存形态、间隙水中氮、磷剖面特征以及沉积物-水界面氮、磷交换特征.结果表明，白洋淀沉积物总氮、总磷含量分别为1230.8~9559.0 mg/kg（均值2379.5 mg/kg）和344.4~915.4 mg/kg（均值608.4 mg/kg），氮、磷累积污染量大.沉积物中铵态氮赋存量大（3.2~175.8 mg/kg），由此导致间隙水中铵态氮浓度较高，最高达到28.8 mg/L.沉积物磷形态以Ca-P和Fe-P为主，分别占总量的38.3%~76.1%和3.98%~18.0%，间隙水中磷酸盐浓度已接近甚至高于国内外典型富营养湖区.间隙水中高浓度的铵态氮和磷酸盐导致沉积物-水界面氮、磷交换通量较高，铵态氮平均释放和扩散通量分别为106.37和12.42 mg/（m2·d）；磷酸盐平均释放和扩散通量分别为15.06和2.33 mg/（m2·d），沉积物内源氮、磷污染负荷较高，已严重威胁到白洋淀水环境质量，迫切需要整治.其中，北部河口区域以及中部府河入湖区和人口密集活动区沉积物氮、磷内源负荷尤为突出，应成为白洋淀沉积物内源污染整治的关键区域. 相似文献
8.
大型浅水湖泊--巢湖内源磷负荷的时空变化特征及形成机制 总被引：7，自引：1，他引：7
通过对大型浅水富营养化湖泊--巢湖湖水、间隙水以及沉积物中磷形态及吸附行为时空变化的研究发现,富营养化较为严重的巢湖西区湖水、间隙水中的正磷酸盐(orthophosphate,Ortho-P)、总磷(total phosphorus,TP)显著高于东湖区,这与西湖区有大量的营养物质通过入湖河道输入有密切关系;此外水柱中颗粒态磷(particulate phosphorus,PP)亦有同样的空间分布规律,且PP的含量与微囊藻的生物量呈显著正相关关系,表明微囊藻在吸收与储藏磷方面比其它藻类更具优势.夏季浮游藻类爆发性增长引起湖水pH的升高以及对磷的大量需求是促使沉积物中的磷(特别是Fe-P)向间隙水中释放的关键因子.沉积物TP、磷形态及吸附行为的空间变化及统计分析的结果表明,沉积物中磷含量的空间异质性与人类活动、土壤地球化学背景及矿物组成等的差异有密切关系.此外,即使沉积物磷含量相同,Fe-P含量的增加将会带来更高的磷释放风险. 相似文献
9.
以典型城市河道(苏州官渎花园内河)为研究对象,通过室内和室外模拟实验,研究不同污染物浓度、流速、曝气复氧、渗滤作用和温度对氮、磷自净能力的影响,结果表明:水体中氮、磷的自净作用受污染物浓度、流速、溶解氧浓度、温度和微生物等多种因素的影响.随着污染物浓度的增加,氨氮和硝态氮降解速率增加,而底泥中磷的总体吸附速率却增大.与静止水体相比,模拟河道通过增加流速、曝气复氧、渗滤作用能增强水体氮磷的自净能力,提高氮、磷降解速率.其中,改变流速后自净参数氨氮和总磷增量分别为17.05%和34.85%;曝气复氧后自净参数氨氮和总磷增量分别为8.35%和59.33%;增加微生物量(渗滤作用)后自净参数氨氮和总磷增量分别为50.00%和23.01%.自然条件下,随着温度的上升,氨氮和总氮的降解系数逐渐增大,总磷的降解系数逐渐减小. 相似文献
10.
微型生态系统中鲢、鳙下行影响的实验研究——2.营养物水平 总被引：4，自引：0，他引：4
鲢、鳙放养使微型生态系统的水柱氮、磷浓度和磷的分布发生了明显的变化。至实验结束时,各实验组的水柱颗粒磷、总磷和氨氮浓度都比对照组高,而正磷酸盐浓度和沉积物磷的量均低于对照组。这种变化以鳙单养系统为最大,其次是鲢、鳙混养系统,鲢单养系统的变化最小。微型生态系统中正磷酸盐浓度同浮游动、植物密度和初级生产力显著相关,氨氮浓度同所述变量之间的相关关系则多半与正磷酸盐相反。实验观测期间浮游植物密度与总磷浓度之间存在营养级联假说所预见的下行影响,实验结束时二者之间却有上行影响的趋向。根据实验观测结果认为,微型生态系统营养物(尤其是磷)水平的变动,主要是鲢、鳙的摄食改变了系统的群属结构和代谢强度的结果,同时反映了实验鱼对系统中营养物再生的影响。 相似文献
11.
Surface area, porosity and water adsorption properties of fine volcanic ash particles 总被引：1，自引：1，他引：0
Our understanding on how ash particles in volcanic plumes react with coexisting gases and aerosols is still rudimentary, despite the importance of these reactions in influencing the chemistry and dynamics of a plume. In this study, six samples of fine ash (<100 m) from different volcanoes were measured for their specific surface area, as, porosity and water adsorption properties with the aim to provide insights into the capacity of silicate ash particles to react with gases, including water vapour. To do so, we performed high-resolution nitrogen and water vapour adsorption/desorption experiments at 77 K and 303 K, respectively. The nitrogen data indicated as values in the range 1.1–2.1 m2/g, except in one case where a as of 10 m2/g was measured. This high value is attributed to incorporation of hydrothermal phases, such as clay minerals, in the ash surface composition. The data also revealed that the ash samples are essentially non-porous, or have a porosity dominated by macropores with widths >500 Å. All the specimens had similar pore size distributions, with a small peak centered around 50 Å. These findings suggest that fine ash particles have relatively undifferentiated surface textures, irrespective of the chemical composition and eruption type. Adsorption isotherms for water vapour revealed that the capacity of the ash samples for water adsorption is systematically larger than predicted from the nitrogen adsorption as values. Enhanced reactivity of the ash surface towards water may result from (i) hydration of bulk ash constituents; (ii) hydration of surface compounds; and/or (iii) hydroxylation of the surface of the ash. The later mechanism may lead to irreversible retention of water. Based on these experiments, we predict that volcanic ash is covered by a complete monolayer of water under ambient atmospheric conditions. In addition, capillary condensation within ash pores should allow for deposition of condensed water on to ash particles before water reaches saturation in the plume. The total mass of water vapour retained by 1 g of fine ash at 0.95 relative water vapour pressure is calculated to be ~10–2 g. Some volcanic implications of this study are discussed.Editorial responsibility: J. Gilbert 相似文献
12.
峡谷分层型水源水库表层沉积物溶解性有机物光谱特征 总被引：7，自引：1，他引：6
结合三维荧光光谱技术（EEMs）与紫外吸收光谱（UV-vis），并利用平行因子分析（PARAFAC）的方法，对金盆水库表层沉积物中溶解性有机质（DOM）光谱的空间分布特征及来源进行分析，并探讨沉积物DOM的荧光组分与可溶性有机氮（SON）、可溶性无机氮（SIN）之间的相关性.结果表明，金盆水库表层沉积物DOM由3类荧光组分组成，分别是类富里酸C1（235 nm，315 nm/430 nm）、类色氨酸C2（220 nm，275 nm/330 nm）和类胡敏酸C3（265 nm/520 nm），各组分荧光强度占总荧光强度百分比的平均值分别为43.15%、31.54%和25.31%.表层沉积物DOM浓度在空间上呈现从上游到主库区先减少后增加的趋势.光谱斜率S275-295、S350-400和光谱斜率比SR反映出各采样点陆源与内源占比的差异性.荧光指数、自生源指标和腐殖化指标都表明金盆水库沉积物DOM的来源具有内源与陆源双重特征.相关性分析表明，表层沉积物DOM各组分与SON和SIN均呈显著正相关，说明DOM与氮元素的迁移转化密切相关. 相似文献
13.
A simple and rapid soft‐templating coupled with one‐pot solvent thermal method is developed to synthesize S‐doped magnetic mesoporous carbon (S‐doped MMC). In this method, phenolic resin is used as a carbon precursor and Pluronic copolymer P123 is used as a template and 2,5‐dimercapto‐1,3,4‐thiadiazole is used as sulfur source. Prepared S‐doped MMC processes a high specific surface area, the Fe3O4 particles are well embedded in the mesoporous carbon walls that exhibit a strong magnetic response, and the hydrated iron nitrate loading amount of 0.808 g is the best. Batch adsorption experiments are carried out at different pH, initial concentration, temperature, and contact time on the adsorption of methyl orange (MO) by S‐doped MMC. The kinetic data of the adsorption process are better fitted with pseudo‐second‐order model than the pseudo‐first‐order model. Langmuir model is more suitable for the equilibrium data than Freundlich model. The thermodynamic parameters including ΔG0, ΔH0, and ΔS0 indicate that the adsorption is a feasible, spontaneous, and endothermic process. Finally, it is found that the coexistence of PO43?, NO3?, SO42?, Cl?, and CO32? does not influence the adsorption process. These results illustrate S‐doped MMC can be an efficient adsorbent for the removal of MO from wastewater. 相似文献
14.
Yebang Xu 《地震学报(英文版)》1992,5(2):389-398
The research of the information dimension (D
1) in an active fault zone considers the contribution of each seismic event to information and reflects the characteristics
of the temporal and spatial distributions of earthquakes from a new point of view, avoiding some short-comings of the research
about the capacity dimension (D
0). The results of calculation show that the information dimension of the temporal distribution in Xianshuihe active fault
zone before Luhuo large earthquake isD
1=0.1051. It is a consult creterion of large earthquakes in future in the fault zone. The information dimensions of the temporal
distribution of the earthquakes in Anninghe active fault zone are respectivelyD
1(t
N)=0.1363 (for the north section) andD
1(t
S)=0.06710 (for the south section). The information dimensions of the spatial distribution are respectivelyD
1(K
N)=1.053 (for the north section) andD
1(K
S)=0.7758 (for the south section). The north section and the south section belong to two self-similar systems with different
information dimensions respectively. The extent of the self-organization of seismic activity in the south section is higher
than that in the north section. This is helpful for us to judge the major dangerous section in the key region of the seismic
monitoring. The research about the information dimension of the temporal and the spatial distributions of earthquakes is significant
for the exploration of active fault zones and seismic prediction.
The Chinese version of this paper appeared in the Chinese edition ofActa Seismologica Sinica,13, 372–379, 1991.
This paper is sponsored by the Chinese Joint Seismological Science Foundation. The English version is improved by Zhenwen
An. 相似文献
15.
C. K. JAIN 《水文科学杂志》2013,58(3):419-434
Abstract A laboratory study was performed to study the effects of various operating factors, viz. initial metal ion concentration, solution pH, amount of sediment, contact time, particle size and temperature on the adsorption of zinc ions onto the bed sediments of the River Ganga (India). The equilibrium time was found to be of the order of 60 min. The adsorption curves are smooth and continuous leading to saturation, suggesting the possible monolayer coverage of zinc ions on the surface of the adsorbent. The extent of adsorption increases with an increase of pH. Furthermore the adsorption of zinc increases with increasing amount of adsorbent and decreases with adsorbent particle size. The important geochemical phases, iron and manganese oxide act as the active support material for the adsorption of zinc ions. The adsorption data have been analysed with the help of Langmuir and Freundlich adsorption models to determine the mechanistic parameters associated with the adsorption process. An attempt has also been made to determine thermodynamic parameters of the process, viz. free energy change, enthalpy change and entropy change. The negative values of free energy change (ΔG°) indicated the spontaneous nature of the adsorption of zinc onto the bed sediments and positive values of enthalpy change (ΔH°) suggest the endothermic nature of the adsorption process. The intraparticle diffusion of zinc in the adsorbent was found to be the main rate-limiting step. 相似文献
16.
城市河流沉积物中氮素与好氧甲烷氧化菌群落特征响应关系 总被引：1，自引：0，他引：1
由于人类活动的影响大量未经处理的废污水汇入城市河流,高浓度的污染物影响了河流中微生物对生物地球化学物质迁移和转化的介导作用.本文选取典型的城市河流——北运河作为研究区域,分析了北运河沉积物中氮素形态以及含量的空间和季节差异性,并结合克隆文库分子生物学的方法,探讨了氮素形态和含量的差异对好氧甲烷氧化菌(aerobic methane-oxidizing microorganisms,MOB)群落特征的影响.结果表明:北运河沉积物中铵态氮(NH_4~+-N)为氮素的主要存在形态,存在显著的空间差异,其含量在下游显著高于上游,但季节差异不显著.NH_4~+-N含量的空间差异对MOB的群落结构和群落分布有显著影响,对群落多样性影响不显著.NH_4~+-N含量的空间分布特征与MOB的群落聚类特征一致,NH_4~+-N对MOB群落分布的影响显著高于其他形态的氮素,其含量越高,则与MOB群落分布的响应关系越紧密.北运河中NH_4~+-N的来源影响了沉积物中MOB的主要来源,MOB高同源性菌群的来源与NH_4~+-N等主要污染物的来源一致.沉积物中MOB物种之间联系的紧密程度依赖于氮素的主要存在形态及其含量水平.NH_4~+-N含量较高的下游沉积物中微生物彼此之间关系及集聚程度更强,受外界环境变化的干扰程度更强,受人类活动引起环境变化的敏感程度更高.城市河流中氮素的形态和含量差异对甲烷的氧化过程有显著影响.探究城市河流沉积物中高含量的NH_4~+-N对甲烷产生及消耗的影响过程是控制河流温室气体排放的关键. 相似文献
17.
为探究富营养化湖泊中自生源可溶有机质(DOM)在泥水界面的吸附行为,以马来眼子菜(Potamogeton malaianus)和铜绿微囊藻(Microcystis aeruginosa)释放的DOM为代表,考察针铁矿对草、藻源DOM中不同组分的吸附特征.三维荧光平行因子分析表明类富里酸组分C1和类胡敏酸组分C4的含量很低,而类蛋白物质(类酪氨酸组分C2和类色氨酸组分C3)分别占草、藻源DOM荧光组成的70%和93%. 2种DOM均可被针铁矿吸附,吸附过程符合伪一级动力学.通过等温线拟合发现针铁矿吸附藻源DOM的非线性更强,饱和吸附量(23.77 mg/g)高于草源DOM(19.10 mg/g).特别地,类蛋白组分呈现非线性吸附,而类腐殖物质的吸附近似线性,且针铁矿对于DOM各荧光组分的吸附量顺序为:C3C2 C4 C1,此非均质吸附特征与DOM组分的初始含量、分子大小、芳香性及有效吸附位点有关.红外光谱证实氨基、羧基和羟基是吸附过程中的重要官能团.因此,草、藻源DOM显著改变了针铁矿表面的有机物质组成,影响湖泊沉积物的生物地球化学行为. 相似文献
18.
Tapan K. Saha Nikhil C. Bhoumik Subarna Karmaker Mahmooda G. Ahmed Hideki Ichikawa Yoshinobu Fukumori 《洁净——土壤、空气、水》2011,39(10):984-993
Adsorption of reactive black 5 (RB5) from aqueous solution onto chitosan was investigated in a batch system. The effects of solution pH, initial dye concentration, and temperature were studied. Adsorption data obtained from different batch experiments were modeled using both pseudo first‐ and second‐order kinetic equations. The equilibrium adsorption data were fitted to the Freundlich, Tempkin, and Langmuir isotherms over a dye concentration range of 45–100 µmol/L. The best results were achieved with the pseudo second‐order kinetic and Langmuir isotherm equilibrium models, respectively. The equilibrium adsorption capacity (qe) was increased with increasing the initial dye concentration and solution temperature, and decreasing solution pH. The chitosan flakes for the adsorption of the dye was regenerated efficiently through the alkaline solution and was then reused for dye removal. The activation energy (Ea) of sorption kinetics was estimated to be 13.88 kJ/mol. Thermodynamic parameters such as changes in free energy (ΔG), enthalpy (ΔH), and entropy (ΔS) were evaluated by applying the van't Hoff equation. The thermodynamics of reactive dye adsorption by chitosan indicates its spontaneous and endothermic nature. 相似文献