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Laboratory batch and column experiments were conducted to investigate the immobilization of phosphorus (P) in soils using synthetic magnetite nanoparticles stabilized with sodium carboxymethyl cellulose (CMC-NP). Although CMC-stabilized magnetite particles were at the nanoscale, phosphorus removal by the nanoparticles was less than that of microparticles (MP) without the stabilizer due to the reduced P reactivity caused by the coating. The P reactivity of CMC-NP was effectively recovered when cellulase was added to degrade the coating. For subsurface non-point P pollution control for a water pond, it is possible to inject CMC-NP to form an enclosed protection wall in the surrounding soils. Non-stabilized “nanomagnetite” could not pass through the soil column under gravity because it quickly agglomerated into microparticles. The immobilized P was 30% in the control soil column, 33% when treated by non-stabilized MP, 45% when treated by CMC-NP, and 73% when treated by both CMC-NP and cellulase. 相似文献
94.
Characterization of plutonium in deep-sea sediments of the Sulu and South China Seas 总被引:1,自引:0,他引:1
Wei Dong Jian Zheng Qiuju Guo Shaoming Pan 《Journal of environmental radioactivity》2010,101(8):622-1899
Anthropogenic Pu isotopes are important geochemical tracers for sediment studies. Their distributions and sources in the water columns as well as the sediments of the North Pacific have been intensively studied; however, information about Pu in the Southeast Asian seas is limited. To study the isotopic composition of Pu, and thus to identify its sources, we collected sediment core samples in the South China Sea and the Sulu Sea during the KH-96-5 Cruise of the R/V Hakuho Maru. We analysed the activities of 239+240Pu and the atom ratios of 240Pu/239Pu using isotope dilution sector-field inductively coupled plasma mass spectrometry (SF-ICP-MS). The 240Pu/239Pu atom ratios in the sediments of both areas (inventory weighted mean: 0.251 for the South China Sea and 0.280 for the Sulu Sea) were higher than the global fallout value (0.178 ± 0.019), suggesting the existence of Pu from the Pacific Proving Grounds in the North Pacific. Low inventories of 239+240Pu in sediments were observed in the South China Sea (3.75 Bq/m2) and the Sulu Sea (1.38 Bq/m2). Most of the Pu input is still present in the water column. Scavenging and benthic mixing processes were considered to be the main processes controlling the distribution of Pu in the deep-sea sediments of both study areas. 相似文献
95.
氨基膦酸树脂是一种常用的广谱性重金属螯合树脂,对水中的Pb(Ⅱ)具有很好的选择性分离去除能力,但吸附Pb(Ⅱ)后的树脂再生较为困难。系统研究了盐酸脱附Pb(Ⅱ)-负载氨基膦酸树脂D860的基本性能,优化了基本脱附参数。实验表明,采用盐酸作为脱附剂具有较为良好的脱附效果,10%吸附量树脂脱附反应平衡较快仅需10 min,脱附本身受Pb(Ⅱ)在盐酸溶液中的溶解度影响显著。脱附流速从1 BV/h升高到5 BV/h,脱附效果受到的影响很小。升高温度可以提高PbCl2溶解度,进而提高脱附效率。固定床脱附采用1.0 mol/L盐酸,在1 BV/h和303 K条件下,仅需7 BV脱附剂即可实现较高的脱附效率。 相似文献
96.
通过静态动力学和热力学吸附实验,研究了温度、共存离子以及溶质的初始浓度对As(V)在金红石TiO2颗粒表面吸附的影响,探讨了As(V)在金红石TiO2颗粒表面吸附特性及机理。结果表明,在As(V)初始浓度为10 mg/L,pH为7的条件下,25℃时的吸附量0.41 mg/g高于30℃时的吸附量0.31 mg/g,As(V)在金红石TiO2上的吸附为放热过程。CaCl2和MgCl2的添加对As(V)在金红石TiO2表面吸附起到明显的促进作用。T=25℃,Ca2+或Mg2+浓度为10 mmol/L时,As(V)吸附量分别为0.64和0.56 mg/g,Ca2+比Mg2+对As(V)吸附促进作用强。As(V)在金红石TiO2的吸附等温线符合Frendlich方程,Lagergren二级动力学方程能较好地描述As(V)在金红石TiO2颗粒表面吸附的动力学过程。 相似文献
97.
Ni2 +对活性污泥活性及群落多样性的影响简 总被引:1,自引:0,他引:1
通过检测活性污泥的电子传递体系活性以及生物多样性,研究Ni2+对活性污泥微生物活性及群落多样性的影响。结果表明:与对照系统相比,5 mg/L的Ni2+对2,3,5-triphenylteltrazolium chloride(TTC-ETS)活性未产生显著的影响;但当Ni2+的浓度进一步增大到10、20和40 mg/L后,其对序批式反应器内活性污泥TTC-ETS活性的抑制率分别达到(36.79±11.14)%、(55.88±13.90)%和(70.97±6.78)%。低浓度Ni2+能增强活性污泥微生物对碳源的利用,但高于10 mg/L的Ni2+则显著抑制了活性污泥微生物对碳源的利用。各个SBR系统中微生物群落最常见的物种相近,物种丰富度和均一性则均有所不同,其中群落物种丰富度随着Ni2+浓度的增加而逐渐减小。TTC-ETS活性、平均每孔颜色变化率、Shannon指数和Simpson指数,与Ni2+的胁迫浓度之间的显著相关性表明,它们均可有效地表征Ni2+胁迫对活性污泥微生物活性及群落多样性的影响程度。 相似文献
98.
为了探索丝状菌的致密途径、解决丝状菌污泥膨胀的难题,从丝状菌的自身特点及外部条件出发研究了其在污泥膨胀及致密过程中菌丝体的演替规律。研究发现,致密生长的大絮体对丝状菌的种类是有选择性的,那些丝体较弯曲、丝体强度较大、贮存能力强的菌丝体更利于形成聚集态生长。另外,研究表明,不同种类丝状菌的生长势和存贮能力不同,对底物的利用上亦存在着竞争关系。实验中存在的几个菌种对PHB颗粒的存贮能力由高到低依次为:Nostocoida limicolaⅡ、Type 1851、Type 0701、Type 021N型菌体。 相似文献
99.
Kuan Lun Pan Sheng Jen Yu Shaw Yi Yan 《Journal of the Air & Waste Management Association (1995)》2014,64(11):1260-1269
Direct decomposition of N2O by perovskite-structure catalysts including La2NiO4, LaSrNiO4, and La0.7Ce0.3SrNiO4 was investigated. The catalysts were prepared by the Pechini method and characterized by x-ray diffraction (XRD), BET, scanning electron microscopy (SEM), and O2-TPD. Experimental results indicate that the properties of La2NiO4 are significantly improved by partially substituting La with Sr and Ce. N2O decomposition efficiencies achieved with LaSrNiO4 and La0.7Ce0.3SrNiO4 are 44 and 36%, respectively, at 400ºC. As the temperature was increased to 600ºC, N2O decomposition efficiency achieved with LaSrNiO4 and La0.7Ce0.3SrNiO4 reached 100% at an inlet N2O concentration of 1,000 ppm, while the space velocity was fixed at 8,000 hr?1. In addition, effects of various parameters including oxygen, water vapor, and space velocity were also explored. The results indicate that N2O decomposition efficiencies achieved with LaSrNiO4 and La0.7Ce0.3SrNiO4 are not significantly affected as space velocity is increased from 8,000 to 20,000 hr?1, while La0.7Ce0.3SrNiO4 shows better tolerance for O2 and H2O(g). On the other hand, N2 yield with LaSrNiO4 as catalyst can be significantly improved by doping Ce. At a gas hour space velocity of 8,000 hr?1, and a temperature of 600ºC, high N2O decomposition efficiency and N2 yield were maintained throughout the durability test of 60 hr, indicating the long-term stability of La0.7Ce0.3SrNiO4 for N2O decomposition.
Implications:Nitrous oxide (N2O) not only has a high global warming potential (GWP100 = 310), but also potentially destroys ozone in the stratosphere. Pervoskite-type catalysts including La2NiO4, LaSrNiO4, and La0.7Ce0.3SrNiO4 are applied for direct N2O decomposition. The results show that N2O decomposition can be enhanced as Sr and Ce are doped into La2NiO4. At 600ºC, N2O decomposition efficiencies achieved with LaSrNiO4 and La0.7Ce0.3SrNiO4 reach 100%, demonstrating high activity and good potential for direct N2O decomposition. Effects of O2 and H2O(g) contents on catalytic activities are also evaluated and discussed. 相似文献
100.
Ting-Long Pan Hong-Shu Wan Zhi-Cheng Ji 《International Journal of Sustainable Engineering》2014,7(2):103-110
This paper presents a stand-alone wind power system with battery/supercapacitor hybrid energy storage. A stand-alone wind power system mainly consists of a wind turbine, a permanent magnet synchronous generator, hybrid energy storage devices based on a vanadium redox flow battery and a supercapacitor, an AC/DC converter, two bidirectional DC/DC converters, a DC/AC converter and a variable load. Several control strategies for the stand-alone wind power system are involved such as a maximum power point tracking (MPPT) control, a vanadium redox flow battery charge/discharge control and a supercapacitor charge/discharge control. The proposed MPPT control combines a sliding mode control with an extreme search control to capture maximum wind energy. This strategy avoids the necessity of measuring wind velocity, obtaining models or parameters of the wind turbine and calculating the differentials of the power generated from the wind power system and from the speed of the generator. The battery charge/discharge control maintains a constant DC bus voltage. When the battery charging/discharging current reaches the setting threshold, the charge/discharge control of the supercapacitor is triggered to limit the charging/discharging current of the battery. The simulation results show that the proposed method can rapidly respond to variations in wind velocity and load power. 相似文献