High-volume Impactor for Sampling Fine and Coarse Particles

Final design, calibration, and field testing have been completed for a new 1.13 m³/min (40 cfm) High-volume Virtual Impactor (HVVI). Field tests have demonstrated that the new classifier/collector works well as an accessory to the existing PM10 Size Selective Inlet high-volume samplers. The HVVI provides two fractions of PM10 mass, both of which are collected by filtration. The fine fraction (0-2.5 μm aero. dia.) Is collected on the standard 20.3 × 25.4 cm (8- × 10-in) high-volume filter; the coarse fraction (2.5-10 μm aero. dia.) is collected on a 5.1 × 15.2 cm (2- × 6-in) filter. Coarse flow through the receiver tubes is limited to 0.057 m³/min (2 cfm), 5 percent of the total flow.

The operating pressure drop across the HVVI stages Is sufficiently high to make changes In pressure across the collection filters Insignificant. The HVVI filter holder assembly facilitates loading/ unloading samples in the laboratory, thus eliminating damage due to handling filters in the field. Size separation characteristics of the HVVI agree well with those for the 16.7 L/min commercially available dichotomous sampler with the 50 percent effectiveness (cut-point) occurring at 2.5 μm. Applying laboratory-determined particle losses to the typical ambient particle mass size distribution described In Federal Register 49, 40 CFR, Part 53, Table D-3, the HVVI fine fraction total mass loss is less than 0.8 percent for liquid particles and less than 0.1 percent for solid particles; coarse fraction total mass loss is less than 2.5 percent for liquid particles, and less than 0.2 percent for solid particles.     

A novel BiVO4-GO-TiO2-PANI composite for upgraded photocatalytic performance under visible light and its non-toxicity

A novel non-toxic hybrid BiVO₄-GO-TiO₂-polyaniline (PANI) (BVGT-PANI) composite with superior photocatalysis was successfully prepared via a one-pot hydrothermal reaction. The structural and morphological characterizations of the synthesized compounds were analyzed by a series of techniques. We found excellent photocatalytic efficiencies for methylene blue (MB) and phenol degradation under visible light irradiation after adhering the PANI to the photocatalyst. The degradation rates of MB and phenol reach up to approximately 85% and 80%, respectively, after 3 h of irradiation. For photodegradation MB, BVGTA exhibit the highest k_app rate constant of about 1.06?×?10^?2 min^?1, which is about 1.63-fold faster than BVG and 2.94-fold faster than BVGT. For photodegradation of phenol, BVGTA exhibits the highest k_app rate constant, of about 8.86?×?10^?3min^?1, which is about 1.2-fold faster than BVG and 1.96-fold faster than BVGT. Furthermore, vitro toxicity test against Bacillus subtilis and Staphylococcus aureus demonstrated that the nanophotocatalyst is non-toxic.

     

Assessing nitrogen and phosphorus removal potential of five plant species in floating treatment wetlands receiving simulated nursery runoff

The feasibility of using floating treatment wetlands (FTWs) to treat runoff typical of commercial nurseries was investigated using two 8-week trials with replicated mesocosms. Plants were supported by Beemat rafts. Five monoculture treatments of Agrostis alba (red top), Canna × generalis ‘Firebird’ (canna lily), Carex stricta (tussock sedge), Iris ensata ‘Rising Sun’ (Japanese water iris), Panicum virgatum (switchgrass), two mixed species treatments, and an unplanted control were assessed. These plant species are used for ornamental, wetland, and biofuel purposes. Nitrogen (N) and phosphorus (P) removals were evaluated after a 7-day hydraulic retention time (HRT). N removal (sum of ammonium-N, nitrate-N, and nitrite-N) from FTW treatments ranged from 0.255 to 0.738 g·m^?2·d^?1 (38.9 to 82.4% removal) and 0.147 to 0.656 g·m^?2·d^?1 (12.9 to 59.6% removal) for trials 1 and 2, respectively. P removal (phosphate-P) ranged from 0.052 to 0.128 g·m^?2·d^?1 (26.1 to 64.7% removal) for trial 1, and 0.074 to 0.194 g·m^?2·d^?1 (26.8 to 63.2% removal) for trial 2. Panicum virgatum removed more N and P than any other FTW treatment and the control in both trials. Results show that species selection and timing of FTW harvest impact the rate and mass of nutrient remediation. FTWs can effectively remove N and P from runoff from commercial nurseries.

     

The Role of Pressure Drop and Flow Redistribution on Modeling Mercury Control Using Sorbent Injection in Baghouse Filters

Abstract

A mathematical model based on simple cake filtration theory was coupled to a reviously developed two-stage mathematical model for mercury (Hg) removal using powdered activated carbon injection upstream of a bag-house filter. Values of the average permeability of the filter cake and the filter resistance extracted from the model were 4.4× 10^?13 m² and 2.5 ×10^?4 m^?1, respectively. The flow is redistributed during partial cleaning of the filter, with flows higher across the newly cleaned filter section. The calculated average Hg removal efficiency from the baghouse is lower because of the high mass flux of Hg exiting the filter in the newly cleaned section. The model shows that calculated average Hg removal is affected by permeability, filter resistance, fraction of the baghouse cleaned, and cleaning interval.     

压裂废水粘度对二氧化锰臭氧催化氧化处理特性的影响

通过FT-IR和GC-MS检测分析,表明了压裂废水中有机物主要以苯环结构为主的芳香类化合物和其他杂环化合物,苯环及杂环上的主要官能团包括酮、酯、羧酸、醛、酚、氨基等。同时,压裂废水中的粘度为常规水粘度的2~3倍。针对压裂废水高粘度和高COD污染水质特征,实验研究了压裂废水二氧化锰臭氧催化氧化处理特性以及粘度对处理效果的影响,研究结果表明,在粘度较高(2.2×10^-3Pa·s)压裂废水中,投加的化学药剂很难扩散,羟基自由基·OH的利用效率较低,处理效果较差。通过投加过硫酸钾(5 g/L)降粘后,可在很大程度上提高二氧化锰臭氧催化氧化的处理效果。通过对压裂废水中有机物分子量分布、FT-IR分析以及GC-MS分析可知,二氧化锰臭氧催化氧化处理压裂废水是通过激发羟基自由基,破坏水中有机物极性和有机物化学构造,将复杂长链有机物转变为简单有机物,其出水COD可达到国家污水综合排放标准中的二级排放标准。     

The capability of estuarine sediments to remove nitrogen: implications for drinking water resource in Yangtze Estuary

Water in the Yangtze Estuary is fresh most of the year because of the large discharge of Yangtze River. The Qingcaosha Reservoir built on the Changxing Island in the Yangtze Estuary is an estuarine reservoir for drinking water. Denitrification rate in the top 10 cm sediment of the intertidal marshes and bare mudflat of Yangtze Estuarine islands was measured by the acetylene inhibition method. Annual denitrification rate in the top 10 cm of sediment was 23.1 μmol m^?2 h^?1 in marshes (ranged from 7.5 to 42.1 μmol m^?2 h^?1) and 15.1 μmol m^?2 h^?1 at the mudflat (ranged from 6.6 to 26.5 μmol m^?2 h^?1). Annual average denitrification rate is higher at mashes than at mudflat, but without a significant difference (p?=?0.084, paired t test.). Taking into account the vegetation and water area of the reservoir, a total 1.42?×?10⁸ g N could be converted into nitrogen gas (N₂) annually by the sediment, which is 97.7 % of the dissolved inorganic nitrogen input through precipitation. Denitrification in reservoir sediment can control the bioavailable nitrogen level of the water body. At the Yangtze estuary, denitrification primarily took place in the top 4 cm of sediment, and there was no significant spatial or temporal variation of denitrification during the year at the marshes and mudflat, which led to no single factor determining the denitrification process but the combined effects of the environmental factors, hydrologic condition, and wetland vegetation.     

容积负荷对ANAMMOX生物滤池脱氮效能的影响及其基质动力学

采用2套启动成功的上向流厌氧氨氧化（ANAMMOX）生物滤柱,通过调节进水NaNO₂和（NH₄）₂SO₄ 的浓度负荷及水力负荷,改变进水容积负荷,探讨容积负荷对ANAMMOX生物滤柱脱氮效能的影响及其动力学模型。结果表明,滤速恒定条件下,通过提高进水基质浓度来提高进水TN容积负荷,其容积负荷去除动力学过程符合Monod-Haldane基质抑制模型。进水NH₄⁺-N与NO₂^--N浓度分别低于100 mg/L和133 mg/L时,反应器脱氮效果不受明显影响,TN容积去除负荷可达4.21 kg/（m³·d）,TN去除率可达80%以上。进水基质浓度恒定条件下,通过提高滤速来提高进水TN容积负荷,其容积负荷去除动力学过程符合零级动力学方程。不受基质浓度抑制的条件下,滤速为3.0 m/h、进水容积负荷为8.82 kg/（m³·d）时,反应器总氮容积负荷去除量可达7.15 kg/（m³·d）,总氮去除率可达81.1%。     

ANAMMOX与反硝化协同作用及氮素负荷研究

向成功启动并稳定运行630 d后的UASB生物膜反应器系统连续添加有机物,分析其对厌氧氨氧化反应脱氮效果的影响,并进行氮素浓度负荷试验.在厌氧氨氧化反应器系统中连续投加有机COD(葡萄糖),系统运行稳定,有机COD(葡萄糖)存在对系统去除氮素能力影响不大,有机COD去除率达到92.0%,仅用23 d,在同一反应器系统中成功实现了厌氧氨氧化与反硝化协同作用脱氮.氮素浓度负荷试验阶段,进水氨氮(NH 4-N)、亚硝氮(NO-2-N)以及总氮(TN)浓度负荷分别从0.063 kg/(m3·d)和0.063 kg/(m3·d)和0.126 kg/(m3·d)提升到了0.239 kg/(m3·d)、0.315 kg/(m3·d)和0.554 kg/(m3·d),相应去除率分别为84.0%、93.0%和85.0%,厌氧氨氧化工艺的UASB生物膜反应器对氮素浓度负荷仍有很大提升空间.     

Neutral poly- and perfluoroalkyl substances in air and seawater of the North Sea

Concentrations of neutral poly- and perfluoroalkyl substances (PFASs), such as fluorotelomer alcohols (FTOHs), perfluoroalkane sulfonamides (FASAs), perfluoroalkane sufonamidoethanols (FASEs), and fluorotelomer acrylates (FTACs), have been simultaneously determined in surface seawater and the atmosphere of the North Sea. Seawater and air samples were taken aboard the German research vessel Heincke on the cruise 303 from 15 to 24 May 2009. The concentrations of FTOHs, FASAs, FASEs, and FTACs in the dissolved phase were 2.6–74, <0.1–19, <0.1–63, and <1.0–9.0 pg L^?1, respectively. The highest concentrations were determined in the estuary of the Weser and Elbe rivers and a decreasing concentration profile appeared with increasing distance from the coast toward the central part of the North Sea. Gaseous FTOHs, FASAs, FASEs, and FTACs were in the range of 36–126, 3.1–26, 3.7–19, and 0.8–5.6 pg m^?3, which were consistent with the concentrations determined in 2007 in the North Sea, and approximately five times lower than those reported for an urban area of Northern Germany. These results suggested continuous continental emissions of neutral PFASs followed by transport toward the marine environment. Air–seawater gas exchanges of neutral PFASs were estimated using fugacity ratios and the two-film resistance model based upon paired air–seawater concentrations and estimated Henry's law constant values. Volatilization dominated for all neutral PFASs in the North Sea. The air–seawater gas exchange fluxes were in the range of 2.5?×?10³–3.6?×?10⁵ pg m^?2 for FTOHs, 1.8?×?10²–1.0?×?10⁵ pg m^?2 for FASAs, 1.1?×?10²–3.0?×?10⁵ pg m^?2 for FASEs and 6.3?×?10²–2.0?×?10⁴ pg m^?2 for FTACs, respectively. These results suggest that the air–seawater gas exchange is an important process that intervenes in the transport and fate for neutral PFASs in the marine environment.     

Deposition fluxes of PCDD/Fs in a reservoir system in northern Taiwan

In this study, polychlorinated dibenzo-p-dioxin and dibenzofuran (PCDD/F) concentrations and depositions in ambient air, water column and sediment were measured at a coupled reservoir-watershed system in northern Taiwan. The atmospheric PCDD/F concentration measured in the vicinity of the reservoir ranged from 4.9 to 39 fg I-TEQ m⁻³ and the Asian dust storm in February accounted for the peak value, which corresponded to a total suspended particle concentration of 128 μg m⁻³. The atmospheric PCDD/F deposition ranged from 1.4 to 19 pg I-TEQ m⁻² d⁻¹, with higher deposition occurring during winter and spring (long-range transport events). During summer, when atmospheric deposition is lower, consecutive tropical cyclones (typhoons) bring heavy rainfall that enhances soil erosion and creates turbidity-driven intermediate flow. This results in significantly higher PCDD/F deposition in water column of the reservoir at 70 m water depth (179 pg I-TEQ m⁻² d⁻¹) than at 20 m (21 pg I-TEQ m⁻² d⁻¹) during typhoon event. The accumulation rate of PCDD/Fs (9.1 ng I-TEQ m⁻² y⁻¹) in the reservoir sediments (depth: 0-2 cm) was consistent with PCDD/F deposition obtained from water column (6.1 and 8.3 ng I-TEQ m⁻² y⁻¹); however, it is significantly higher when compared to the atmospheric deposition (2.0 ng I-TEQ m⁻² y⁻¹). Based on the mass balance between the measurements of atmospheric deposition and sinking particles in water column, around 54-74% of PCDD/F inputs into the reservoir were contributed by the catchment erosion during normal period. However, the PCDD/F input contributed by the enhanced catchment erosion significantly increased to 90% during intensive typhoon events.     

人工湿地植物泌氧与污染物降解耗氧关系研究

实验采用静态水培方法研究了香蒲(Typha orientalis)、芦苇(Phragmites australis)和水葱(Scirpus validus)3种常见湿地水生植物潜在泌氧能力、去污效果,并对水生植物泌氧量与污染物降解耗氧量进行了计算分析,从而阐明湿地植物泌氧与污染物降解耗氧之间的关系。结果表明,3种植物泌氧能力由大到小依次为:芦苇香蒲水葱,其中,芦苇比放氧速率、面积泌氧率均最高,分别为3.36 mg O2/(g.d)和4.35 g O2/(m2.d)。植物对湿地系统中污染物的去除有重要影响,各植物系统COD去除速率在3.46~3.77 g/(m2.d)之间;NH4+-N去除速率在0.07~0.13 g/(m2.d);TN去除速率在0.25~0.27 g/(m2.d);TP去除速率均为0.09 g/(m2.d);均好于无植物空白系统。计算表明,各植物体系泌氧量在0.48~0.55 g O2/d之间;各植物体系COD、NH4+-N耗氧量在0.41~0.46 g O2/d之间;植物净泌氧量在0.02~0.12 g O2/d之间。植物泌氧量与COD、NH4+-N耗氧量呈显著正相关关系。若应用人工湿地处理城镇生活污水,各植物体系COD最大去除负荷在3.81~4.35 g/(m2.d)之间,NH4+-N最大去除负荷在0.83~0.95 g/(m2.d)之间,最大水力负荷在1.65~1.89 cm/d之间。     

Photocatalytic degradation of contaminants of concern with composite NF-TiO2 films under visible and solar light

This study reports the synthesis and characterization of composite nitrogen and fluorine co-doped titanium dioxide (NF-TiO₂) for the removal of contaminants of concern in wastewater under visible and solar light. Monodisperse anatase TiO₂ nanoparticles of different sizes and Evonik P25 were assembled to immobilized NF-TiO₂ by direct incorporation into the sol–gel or by the layer-by-layer technique. The composite films were characterized with X-ray diffraction, high-resolution transmission electron microscopy, environmental scanning electron microscopy, and porosimetry analysis. The photocatalytic degradation of atrazine, carbamazepine, and caffeine was evaluated in a synthetic water solution and in an effluent from a hybrid biological concentrator reactor (BCR). Minor aggregation and improved distribution of monodisperse titania particles was obtained with NF-TiO₂-monodisperse (10 and 50 nm) from the layer-by-layer technique than with NF-TiO₂?+?monodisperse TiO₂ (300 nm) directly incorporated into the sol. The photocatalysts synthesized with the layer-by-layer method achieved significantly higher degradation rates in contrast with NF-TiO₂-monodisperse titania (300 nm) and slightly faster values when compared with NF-TiO₂-P25. Using NF-TiO₂ layer-by-layer with monodisperse TiO₂ (50 nm) under solar light irradiation, the respective degradation rates in synthetic water and BCR effluent were 14.6 and 9.5?×?10^?3?min^?1 for caffeine, 12.5 and 9.0?×?10^?3?min^?1 for carbamazepine, and 10.9 and 5.8?×?10^?3?min^?1 for atrazine. These results suggest that the layer-by-layer technique is a promising method for the synthesis of composite TiO₂-based films compared to the direct addition of nanoparticles into the sol.     

The contribution of elemental carbon to the optical properties of rural atmospheric aerosols

Measurements of carbonaceous aerosol, aerosol light absorption and aerosol light scattering were made at two rural sites in southwestern Pennsylvania during August 1983. Aerosol light absorption ranged from 5.2 × 10⁻⁶ m⁻¹ to 6.4 × 10⁻⁵ m⁻¹ (average: 1.9 × 10⁻⁵ m⁻¹) and accounted for about 13% of the aerosol total light extinction. Elemental carbon, averaging 1.3 μg m⁻³ at the two sites (and comprising some 36 % of the aerosol carbon), accounted for effectively all (> 95 %) of the aerosol light absorption.     

Ultrasonic decomposition of atrazine and alachlor in water.

Abstract

The collapse of ultrasonically‐generated cavitation bubbles can result in sonochemical reactions. The kinetics of sonochemical decomposition of alachlor and atrazine in water were determined using a sonicator operating in the continuous mode at maximum output. Alachlor and atrazine solutions, 3.1 nmol L^‐1, were kept at constant temperature during the sonication. Decomposition at 30°C followed first‐order kinetics: k = 8.01 × 10^‐3 min^‐1 and 2.10 × 10^‐3 min^‐1 for alachlor and atrazine, respectively. It is not clear from the product analysis whether the decomposition was due to a thermal or free radical reaction. However, regardless of the decomposition mechanisms, the extrapolated half‐lives (86 and 330 min for alachlor and atrazine, respectively) support the potential development of ultrasonic waves to decompose herbicides in contaminated water.     

Atrazin Atmospheric deposition and air-borne concentrations

Am Beispiel des Wirkstoffes Atrazin wird die atmosph?rische Verbreitung und der atmosph?rische Eintrag von Pflanzenschutzmitteln mit einer geringen Flüchtigkeit aufgezeigt. Immissions-Konzentrationen lagen zwischen weniger als 0.005 ng·m⁻³ und maximal 0.32 ng·m⁻³ Atrazin wird fast ausschlie?lich in der Partikelphase, offensichtlich im Ungleichgewicht mit der Gasphase, verfrachtet. Dies verz?gert wahrscheinlich den photochemischen Abbau in der Atmosph?re. Die Konzentrationen im Flüssigwasser aufliegender Wolken erreichten zu den Applikationsterminen nahezu 1.6 μg·1⁻¹. Die Eintr?ge über die Atmosph?re betrugen in exponierter Lage im Fichtelgebirge mit 0.13 mg·m⁻²·a⁻¹ ca. 0.4% der Aufwandmengen in 3j?hrigen Maisfruchtfolgen. Im Alpenraum wurden mit 0.012 mg·m⁻²·a⁻¹ deutlich niedrigere Frachten gemessen als im Fichtelgebirge.Das Umweltrisiko durch die atmosph?rische Verbreitung und Deposition von Atrazin und anderen Pflanzenschutzmitteln mit vergleichbaren physikalisch-chemischen Eigenschaften ist als ?u?erst gering einzustufen. Atmospheric occurrence and deposition of atrazine are measured. During the application of atrazine, highest concentrations reached 1.6 μg·1⁻¹ in liquid water of lowlying clouds touching mountain tops. Atmospheric deposition, however, hardly amounts to 0.4% of the flux on crop land by direct spraying. Airborne concentrations ranged from less than 0.005 ng·m⁻³ to 0.32 ng·m⁻³. Contrary to theoretical expectations, almost all atrazine was found in the particulate matter, indicating nonequilibrium with the gas phase. This may inhibit a rapid photochemical decomposition. Human health concerns and environmental risks due to the atmospheric occurrence and deposition of atrazine are judged as minor. This conclusion can be applied to many other, physicochemically related pesticides.     

活性炭纤维生物挂膜脱除硫化氢

生物脱硫法作为一种高效、高实用性的除硫新技术而受到越来越多的关注。以活性炭纤维为微生物载体,通过活性污泥上清液挂膜驯化,考察硫化氢进气量、喷淋量、pH值和硫酸根离子浓度等条件对脱硫效率的影响。研究结果表明,在室温下,硫化氢负荷为90 g/(m3.h),进气浓度控制在3 g/m3,进气量为60 L/h,喷淋量为250～650 L/(m3.d),pH为2～5的条件下,生物活性炭纤维对硫化氢的去除率可保持在98%以上。     

Evaluation of Biopolymer-Modified Concrete Systems for Disposal of Cathode Ray Tube Glass

Abstract

Cathode ray tubes (CRTs) from computer monitors and television sets, which contain significantly high percentage of lead (Pb) by weight, represent an enormous and growing hazardous waste problem in the United States and worldwide. As a result, new technologies are needed to cope with current CRT waste stream and increased hazard and build new markets for its recycled components, developing commercially viable concrete composites, as well as minimizing CRT disposal problems. In this study, commercially available biopolymers, such as xan-than gum, guar gum, and chitosan, were used to encapsulate CRT glass waste, reducing the Pb leachability. The biopolymers utilized contain a number of useful functional groups, such as carboxyl (xanthan), hydroxyl (guar), and amino groups (chitosan), which play important roles in binding and stabilizing Pb onto concrete structures. The use of biopolymers in concrete systems can create a stable interpenetrating cross-linking composite that will last for many years. Results from these new composites show 30% higher compressive strength than standard concrete and a sharp decrease in lead leachability from several thousand milligrams per liter initially to an amount of three-tenths milligrams per liter or lower values (much lower than the U.S. Environment Protection Agency standard for hazardous waste of 5 mg/L by the toxicity characteristic leaching procedure test), and for some of the composites leachability is below even the standard for drinking water. This efficient and cost-effective CRT–biopolymer-concrete composite is a new class of biopolymer-modified material that can potentially perform a significant role in relieving the current CRT issue.     

Comparison of modeling with empirical calculation of diffuse and fugitive methane emissions in a Spanish landfill

One of the most significant environmental problems arising from landfills is the emission of methane into the atmosphere. In this study, methane emissions from a currently in-use Spanish landfill were modeled as well as being experimentally measured using a two-step method. The first step involved a qualitative walkover survey to detect where gases were being emitted on the surface of the landfill. The second stage comprised a quantitative analysis of these surface methane emissions at a selected number of points on the landfill surface using a specially designed flux chamber. The statistical analysis of the data obtained was based on the Sichel function and resulted in an average emission rate of 74.9 g·m^?2·day^?1, with 27.8 and 202.1 g·m^?2·day^?1 as the lower and upper limits of the 95% confidence interval, respectively. The total emission for the landfill, with an emitting surface of 335,000 m², is 9.16 × 10³ ton/yr. These values have been compared with those from three different models, with the model results being above the calculated mean emissions measured at the landfill, but below the upper confidence limit at 95%.

Implications: One of the main environmental problems arising from the presence of landfills is the emission of biogas (which mainly contains methane and carbon dioxide) into the atmosphere. Several experimental methods as well as models have been developed to quantify these emissions. In this work, the authors have compared the results obtained using experimental measurements with those provided by some local and international models using the default parameters proposed. The results obtained from the experimental method are in accordance with those provided by the models, although the models could be slightly overestimating these emissions.     

组合型生态浮床对水体修复及植物氮磷吸收能力研究

在天鹅湖水体中构建以水生植物和陆生喜水植物为实验植物,浮法控制器、水循环增氧系统和造浪-输送系统相集合的组合型生态浮床。在中试研究中,研究了其对天鹅湖上覆水和沉积物中营养物质的修复动态。结果表明,经过4个多月的组合型生态浮床生态修复,天鹅湖上覆水中TN、NH4+-N和TP的去除率分别达到61.92%、63.09%和80.0%,沉积物中TN和NH4+-N含量的去除率分别达到23.79%和37.04%,TP含量升高了43.71%;组合型生态浮床的5种浮床植物的氮磷累积量差异显著,再力花和美人蕉对氮磷的吸收速率显著高于菖蒲、薄荷和水稻,再力花和美人蕉对氮的吸收速率达到12.19 g/(m2.d)和7.90 g/(m2.d),对磷吸收分别达到0.81 g/(m2.d)和0.99 g/(m2.d)。美人蕉和再力花对氮磷的吸收量均是茎叶>根系,其中美人蕉茎叶氮、磷吸收量分别为根系的2.73倍和1.93倍,再力花分别为1.83倍和1.19倍,通过浮床系统植物水上部分的收割可以去除水体中的氮磷。     

Characterization of Activated Carbon Fiber Filters for Pressure Drop,Submicrometer Particulate Collection,and Mercury Capture

ABSTRACT

The use of activated carbon fiber (ACF) filters for the capture of particulate matter and elemental Hg is demonstrated. The pressure drop and particle collection efficiency characteristics of the ACF filters were established at two different face velocities and for two different aerosols: spherical NaCl and combustion-generated silica particles. The clean ACF filter specific resistance was 153 kg m^-2 sec^-1. The experimental specific resistance for cake filtration was 1.6 × 10⁶ sec^-1 and 2.4 × 10⁵ sec^-1 for 0.5- and 1.5-μm mass median diameter particles, respectively. The resistance factor R was approximately 2, similar to that for the high-efficiency particulate air filters. There was a discrepancy in the measured particle collection efficiencies and those predicted by theory. The use of the ACF filter for elemental Hg capture was illustrated, and the breakthrough characteristic was established. The capacity of the ACF filter for Hg capture was similar to other powdered activated carbons.