Nitrogen Removal in a Horizontal Subsurface Flow Constructed Wetland Estimated Using the First-Order Kinetic Model

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Lijuan Cui

2016-11-01

Full Text Available We monitored the water quality and hydrological conditions of a horizontal subsurface constructed wetland (HSSF-CW in Beijing, China, for two years. We simulated the area-based constant and the temperature coefficient with the first-order kinetic model. We examined the relationships between the nitrogen (N removal rate, N load, seasonal variations in the N removal rate, and environmental factors—such as the area-based constant, temperature, and dissolved oxygen (DO. The effluent ammonia (NH4+-N and nitrate (NO3−-N concentrations were significantly lower than the influent concentrations (p < 0.01, n = 38. The NO3−-N load was significantly correlated with the removal rate (R2 = 0.96, p < 0.01, but the NH4+-N load was not correlated with the removal rate (R2 = 0.02, p > 0.01. The area-based constants of NO3−-N and NH4+-N at 20 °C were 27 ± 26 (mean ± SD and 14 ± 10 m∙year−1, respectively. The temperature coefficients for NO3−-N and NH4+-N were estimated at 1.004 and 0.960, respectively. The area-based constants for NO3−-N and NH4+-N were not correlated with temperature (p > 0.01. The NO3−-N area-based constant was correlated with the corresponding load (R2 = 0.96, p < 0.01. The NH4+-N area rate was correlated with DO (R2 = 0.69, p < 0.01, suggesting that the factors that influenced the N removal rate in this wetland met Liebig’s law of the minimum.

Nitrogen removal and nitrate leaching for forage systems receiving dairy effluent.

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Woodard, Kenneth R; French, Edwin C; Sweat, Lewin A; Graetz, Donald A; Sollenberger, Lynn E; Macoon, Bisoondat; Portier, Kenneth M; Wade, Brett L; Rymph, Stuart J; Prine, Gordon M; Van Horn, Harold H

2002-01-01

Florida dairies need year-round forage systems that prevent loss of N to ground water from waste effluent sprayfields. Our purpose was to quantify forage N removal and monitor nitrate N (NO3(-)-N) concentrations in soil water below the rooting zone for two forage systems during four 12-mo cycles (1996-2000). Soil in the sprayfield is an excessively drained Kershaw sand (thermic, uncoated Typic Quartzipsamment). Over four cycles, average loading rates of effluent N were 500, 690, and 910 kg ha(-1) per cycle. Nitrogen removed by the bermudagrass (Cynodon spp.)-rye (Secale cereale L.) system (BR) during the first three cycles was 465 kg ha(-1) per cycle for the low loading rate, 528 kg ha(-1) for the medium rate, and 585 kg ha(-1) for the high. For the corn (Zea mays L.)-forage sorghum [Sorghum bicolor (L.) Moench]-rye system (CSR), N removals were 320 kg ha(-1) per cycle for the low rate, 327 kg ha(-1) for the medium, and 378 kg ha(-1) for the high. The higher N removals for BR were attributed to higher N concentration in bermudagrass (18.1-24.2 g kg(-1)) than in corn and forage sorghum (10.3-14.7 g kg(-1)). Dry matter yield declined in the fourth cycle for bermudagrass but N removal continued to be higher for BR than CSR. The BR system was much more effective at preventing NO3(-)-N leaching. For CSR, NO3(-)-N levels in soil water (1.5 m below surface) increased steeply during the period between the harvest of one forage and canopy dosure of the next. Overall, the BR system was better than CSR at removing N from the soil and maintaining low NO3(-)-N concentrations below the rooting zone.

Comparison of nitrogen removal rates and nitrous oxide production from enriched anaerobic ammonium oxidizing bacteria in suspended and attached growth reactors.

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Panwivia, Supaporn; Sirvithayapakorn, Sanya; Wantawin, Chalermraj; Noophan, Pongsak Lek; Munakata-Marr, Junko

2014-01-01

Attached growth-systems for the anaerobic ammonium oxidation (anammox) process have been postulated for implementation in the field. However, information about the anammox process in attached growth-systems is limited. This study compared nitrogen removal rates and nitrous oxide (N2O) production of enriched anammox cultures in both suspended and attached growth sequencing batch reactors (SBRs). Suspended growth reactors (SBR-S) and attached growth reactors using polystyrene sponge as a medium (SBR-A) were used in these experiments. After inoculation with an enriched anammox culture, significant nitrogen removals of ammonium (NH4 (+)) and nitrite (NO2 (-)) were observed under NH4 (+):NO2 (-) ratios ranging from 1:1 to 1:2 in both types of SBRs. The specific rates of total nitrogen removal in SBR-S and SBR-A were 0.52 mg N/mg VSS-d and 0.44 mg N/mg VSS-d, respectively, at an NH4 (+):NO2 (-) ratio of 1:2. N2O production by the enriched anammox culture in both SBR-S and SBR-A was significantly higher at NH4 (+):NO2 (-) ratio of 1:2 than at NH4 (+):NO2 (-) ratios of 1:1 and 1:1.32. In addition, N2O production was higher at a pH of 6.8 than at pH 7.3, 7.8, and 8.3 in both SBR-S and SBR-A. The results of this investigation demonstrate that the anammox process may avoid N2O emission by maintaining an NH4 (+):NO2 (-) ratio of less than 1:2 and pH higher than 6.8.

Time resolved LIF measurements for the study of NO removal: influence of H2O

International Nuclear Information System (INIS)

Fresnet, F.; Baravian, G.; Magne, L.; Pasquiers, S.; Postel, C.; Puech, V.; Rousseau, A.

2001-01-01

We have developed a time-resolved laser-induced fluorescence (LIF) diagnostic of the NO-removal in a pre-ionized homogeneous discharge, i.e. without density nor temperature gradients, using the photo-triggering technique. This technique allows to measure specie densities in the temporal post-discharge after one homogeneous pulsed excitation, so that experimental results can be more confidently compared to predictions of a 0D-model, i.e. a model which have a spatially homogeneous kinetic description of the cleaning process. This model is fully self-consistent and describe both kinetics during the discharge and the post-discharge. We first reported the influence of electrical parameters (energy and reduced electric field) on the NO removal efficiency in the N 2 /NO mixture. Then, the influence of hydrocarbon (C 2 H 4 ) addition was determined. We showed that dissociation of NO through collision with the metastable state N 2 (a '1 Σ u - ) play the main part in the NO-removal process in homogeneously excited N 2 /NO mixture, and, that a de-excitation process of N 2 (a '1 Σ u - ) by C 2 H 4 explains that the NO-removal efficiency decreases when ethene is added to the mixture. Estimation for the rate coefficient value of this reaction, closed to the known value for methane, was also deduced from our results. In this study, the influence of water is investigated on the NO removal efficiency

Variable lifetimes and loss mechanisms for NO3 and N2O5 during the DOMINO campaign: contrasts between marine, urban and continental air

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Crowley, J. N.; Thieser, J.; Tang, M. J.; Schuster, G.; Bozem, H.; Beygi, Z. H.; Fischer, H.; Diesch, J.-M.; Drewnick, F.; Borrmann, S.; Song, W.; Yassaa, N.; Williams, J.; Pöhler, D.; Platt, U.; Lelieveld, J.

2011-11-01

Nighttime mixing ratios of boundary layer N2O5 were determined using cavity-ring-down spectroscopy during the DOMINO campaign in Southern Spain (Diel Oxidant Mechanisms In relation to Nitrogen Oxides, 21 November 2008-8 December 2008). N2O5 mixing ratios ranged from below the detection limit (~5 ppt) to ~500 ppt. A steady-state analysis constrained by measured mixing ratios of N2O5, NO2 and O3 was used to derive NO3 lifetimes and compare them to calculated rates of loss via gas-phase and heterogeneous reactions of both NO3 and N2O5. Three distinct types of air masses were encountered, which were largely marine (Atlantic), continental or urban-industrial in origin. NO3 lifetimes were longest in the Atlantic sector (up to ~30 min) but were very short (a few seconds) in polluted, air masses from the local city and petroleum-related industrial complex of Huelva. Air from the continental sector was an intermediate case. The high reactivity to NO3 of the urban air mass was not accounted for by gas-phase and heterogeneous reactions, rates of which were constrained by measurements of NO, volatile organic species and aerosol surface area. In general, high NO2 mixing ratios were associated with low NO3 lifetimes, though heterogeneous processes (e.g. reaction of N2O5 on aerosol) were generally less important than direct gas-phase losses of NO3. The presence of SO2 at levels above ~2 ppb in the urban air sector was always associated with very low N2O5 mixing ratios indicating either very short NO3 lifetimes in the presence of combustion-related emissions or an important role for reduced sulphur species in urban, nighttime chemistry. High production rates coupled with low lifetimes of NO3 imply an important contribution of nighttime chemistry to removal of both NOx and VOC.

Variable lifetimes and loss mechanisms for NO3 and N2O5 during the DOMINO campaign: contrasts between marine, urban and continental air

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J. Williams

2011-11-01

Full Text Available Nighttime mixing ratios of boundary layer N2O5 were determined using cavity-ring-down spectroscopy during the DOMINO campaign in Southern Spain (Diel Oxidant Mechanisms In relation to Nitrogen Oxides, 21 November 2008–8 December 2008. N2O5 mixing ratios ranged from below the detection limit (~5 ppt to ~500 ppt. A steady-state analysis constrained by measured mixing ratios of N2O5, NO2 and O3 was used to derive NO3 lifetimes and compare them to calculated rates of loss via gas-phase and heterogeneous reactions of both NO3 and N2O5. Three distinct types of air masses were encountered, which were largely marine (Atlantic, continental or urban-industrial in origin. NO3 lifetimes were longest in the Atlantic sector (up to ~30 min but were very short (a few seconds in polluted, air masses from the local city and petroleum-related industrial complex of Huelva. Air from the continental sector was an intermediate case. The high reactivity to NO3 of the urban air mass was not accounted for by gas-phase and heterogeneous reactions, rates of which were constrained by measurements of NO, volatile organic species and aerosol surface area. In general, high NO2 mixing ratios were associated with low NO3 lifetimes, though heterogeneous processes (e.g. reaction of N2O5 on aerosol were generally less important than direct gas-phase losses of NO3. The presence of SO2 at levels above ~2 ppb in the urban air sector was always associated with very low N2O5 mixing ratios indicating either very short NO3 lifetimes in the presence of combustion-related emissions or an important role for reduced sulphur species in urban, nighttime chemistry. High production rates coupled with low lifetimes of NO3 imply an important contribution of nighttime chemistry to removal of both NOx and VOC.

Removal of NO2 and O3 generated from corona discharge in indoor air cleaning with MnO2 catalyst

International Nuclear Information System (INIS)

Ge, H; Yu, R; Zhu, Y M; Mi, D

2013-01-01

The production rules and removal efficiency of harmful byproducts such as NO 2 and O 3 generated from DC corona discharge in indoor air cleaning were investigated. The production behaviours of NO 2 and O 3 and the relationship between the amount of catalyst (MnO 2 ) and the removal rate of harmful byproducts were experimentally studied. Further, indoor application tests were carried out in a closed room with 90 m 3 . The results showed that the concentrations of NO 2 and O 3 produced by corona discharge linearly increased with discharge time. The NO 2 yield is larger than O 3 by almost one order of magnitude under the same discharge power. To satisfy the demand of Standard of Indoor Air Quality (GB/T18883-2002), the power consumption of unit volume should be less than 1 W m −3 and the catalyst MnO 2 consumptions in positive-negative corona discharge were 200 cm 3 W −1 and 100 cm 3 W −1 , respectively.

New polymer for removal of wine phenolics: Poly(N-(3-(N-isobutyrylisobutyramido)-3-oxopropyl)acrylamide) (P-NIOA).

Science.gov (United States)

Castro, Ricardo I; Forero-Doria, Oscar; Guzmán, Luis; Laurie, V Felipe; Valdés, Oscar; Ávila-Salas, Fabián; López-Cortés, Xaviera; Santos, Leonardo S

2016-12-15

The phenolic compounds of wine contribute to color and astringency, also are responsible for the oxidation state and bitterness. Due the importance of these molecules, different techniques have been used to modulate their concentration such as natural or synthetic polymeric agents. Among the polymeric agents, PVPP is one of the most used, but lacks of selectivity and has a limited pH range. Therefore, the aim of this study was the synthesis of a new polymer, poly(N-(3-(N-isobutyrylisobutyramido)-3-oxopropyl)acrylamide) (P-NIOA), for removal of phenolic compounds, as a potential agent for the fining of wine. The new polymer affinity was studied using HPLC-DAD for different polyphenols using PVPP as a control. The results showed that the new polymer has a similar removal as PVPP, but with lower affinity to resveratrol. The interactions established between polymers and polyphenols were studied using computational chemistry methods demonstrating a direct correlation with the experimental affinity data. Copyright © 2016 Elsevier Ltd. All rights reserved.

Visible-light-driven N-(BiO)2CO3/Graphene oxide composites with improved photocatalytic activity and selectivity for NOx removal

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Chen, Meijuan; Huang, Yu; Yao, Jie; Cao, Jun-ji; Liu, Yuan

2018-02-01

N-doped (BiO)2CO3 (NBOC)/graphene oxide (GO) composite obtained from three-dimensional hierarchical microspheres is successfully synthesized by one-pot hydrothermal method for the first time. In this synthesis, citrate ion plays a critical role in N doping. The obtained samples are used to degrade gaseous nitrogen oxides (NOx) at parts-per-billion (ppb) level under visible-light irradiation. NBOC-GO composite with 1.0 wt% graphene oxide (GO) displays the highest photocatalytic NO removal efficiency, which is 4.3 times higher than that of pristine (BiO)2CO3. Moreover, NBOC-GO composite significantly inhibits toxic NO2 intermediate production, indicating its high selectivity for NO conversion. Compared with regular GO, N doping considerably improves the catalytic performance of NBOC-GO composite, which increases NO removal by 74.6% and fully inhibits NO2 generation. The improved photocatalytic activity is mainly ascribed to extended optical absorption ability and enhanced separation efficiency of photogenerated charge carriers over NBOC-GO composite. Both results of electron spin resonance and theoretical analysis of band structure indicate that NO removal is dominated by oxidation with rad OH and rad O2- radicals. The photocatalytic activity improvement mechanism over the NBOC-GO composite is proposed accordingly based on systematic characterizations. This study demonstrates a feasible route to fabricating Bi-containing composites with high selectivity and stability for air pollution control and provides a new insight into the associated photocatalytic mechanisms.

[Removal of nitrate from groundwater using permeable reactive barrier].

Science.gov (United States)

Li, Xiu-Li; Yang, Jun-Jun; Lu, Xiao-Xia; Zhang, Shu; Hou, Zhen

2013-03-01

To provide a cost-effective method for the remediation of nitrate-polluted groundwater, column experiments were performed to study the removal of nitrate by permeable reactive barrier filled with fermented mulch and sand (biowall), and the mechanisms and influence factors were explored. The experimental results showed that the environmental condition in the simulated biowall became highly reduced after three days of operation (oxidation-reduction potential was below - 100 mV), which was favorable for the reduction of nitrate. During the 15 days of operation, the removal rate of nitrate nitrogen (NO3(-) -N) by the simulated biowall was 80%-90% (NO3(-)-N was reduced from 20 mg x L(-1) in the inlet water to 1.6 mg x L(-1) in the outlet water); the concentration of nitrite nitrogen (NO2(-) -N) in the outlet water was below 2.5 mg x L(-1); the concentration of ammonium nitrogen (NH4(+) -N) was low in the first two days but increased to about 12 mg x L(-1) since day three. The major mechanisms involved in the removal of nitrate nitrogen were adsorption and biodegradation. When increasing the water flow velocity in the simulated biowall, the removal rate of NO3(-) -N was reduced and the concentration of NH4(+) -N in the outlet water was significantly reduced. A simulated zeolite wall was set up following the simulated biowall and 98% of the NH4(+) -N could be removed from the water.

Comparative study of wheat utilization of NH4 and NO3 as sources of N-fertilizer using N15 technique

International Nuclear Information System (INIS)

Khalifa, Kh.

1993-05-01

Two field experiments were conducted separately on wheat (Cultivar ACSAD-65) in 1987/1988 at the Research Station of Arabic Center for the Studies of Arid Zones and Dry Lands (ACSAD) in Deir-Ezzor, Using N 15 methodology to compare the efficient utilization of N 15 -NO 3 and N 15 -N H 4 radicals as sources of nitrogen applied in three different levels (50, 100 and 200 Kg N/ha and two placement methods (Top-dressed and Side-dressed). The results indicate that Ndff % in the from of N 15 -NH 4 was higher than N 15 -NO 3 in both placements, at different growth stages, consequently, when using N-NH 4 form, N-uptake was higher than N-NO 3 form; the efficiency of N-NH 4 was higher than N-NO 3 in most cases regardless of the method of placement; the rate of applied nitrogen in both forms (N-NH 4 and N-NO 3 ) had higher effect on yield more than the placements; side-dressed placement had higher effect on the efficiency of the utilization of N-NO 3 and N-NH 4 as well as on crop yield than the Top-dressed; using N-NO 3 , A-values in the three growth stages of crop at the nitrogen levels used, were higher than using N-NH 4 in both placements; and finally using N-NO 3 in the second and third stages of crop growth, the yield was higher than using N-NH 4 and almost similar in the first stages. (author). 9 refs., 26 tabs

Oxidative removal of quinclorac by permanganate through a rate-limiting [3 + 2] cycloaddition reaction.

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Song, Dean; Cheng, Hanyang; Jiang, Xiaohua; Sun, Huiqing; Kong, Fanyu; Liang, Rongning; Qiang, Zhimin; Liu, Huijuan; Qu, Jiuhui

2018-04-05

Quinclorac, a widely used herbicide in agriculture, has been recognized as an emerging environmental pollutant owing to its long persistence and potential risk to humans. However, no related information is available on the degradation of quinclorac by employing oxidants. Herein, the reactivity of quinclorac with permanganate was systematically investigated in water by combining experimental and computational approaches. The reaction followed overall second-order kinetics pointing to a bimolecular rate-limiting step. The second-order rate constant was found to be 3.47 × 10-3 M-1 s-1 at 25 °C, which was independent of pH over the range from 5 to 9 and was dependent on temperature over the range from 19 to 35 °C. The initial product was identified by UPLC-Q-TOF-MS to be mono-hydroxylated quinclorac, which was more susceptible to further oxidation. The result could be supported by the complete simulation of the reaction process in DFT calculations, indicating the [3 + 2] cycloaddition oxidation of the benzene ring in the rate-limiting step. The plausible mechanism was then proposed, accompanied by the analysis of the HOMO indicating the hydroxylation position and of the ESP suggesting a more electron-rich moiety. Considering the high effectiveness and low toxicity, permanganate oxidation was considered to be a very promising technique for removing quinclorac from aquatic environments.

Premelting, Melting, and Degradation Properties of Molten Alkali Nitrates: LiNO3, NaNO3, KNO3, and Binary NaNO3-KNO3

Science.gov (United States)

Mohammad, Mehedi Bin; Brooks, Geoffrey Alan; Rhamdhani, Muhammad Akbar

2018-02-01

A simultaneous thermal analyzer (STA) was used to observe the transition and degradation events of LiNO3, NaNO3, KNO3, and binary NaNO3-KNO3 salts for potential use as phase change materials (PCMs) and heat transfer fluid (HTF). Samples were heated from 50 °C to 800 °C at 10 °C/min scanning rate in three atmospheres (argon, air, and oxygen) using an STA to observe decomposition behavior. Thermal stability increased for all salts at high partial pressure of O2 ( P_{{{O}2 }} = 1.0) compared to inert argon ( P_{{{O}2 }} = 0). O2, N2, NO, N2O, and NO2 were main evolved gases during nitrate decomposition. NO and O2 started to evolve at approximately the same temperature after melting, indicating that primary and secondary decomposition reactions were concurrent and overlapping. The solid-solid transition, liquidus and solidus temperatures, heat of transition, heat of melting, and heat of solidification were obtained at various heating-cooling rates (1, 2, 4, 5, 6, 8, 10, and 15 °C/min) using an STA. At all heating-cooling rates, a small gap exists between liquidus and solidus temperatures for all samples due to the salts exhibiting supercooling phenomena. This study showed that the degradation point depends on the blanket atmosphere top of the molten salts and that heating rates have a minor effect on transition events (peaks height, peaks width, and transition enthalpies).

Premelting, Melting, and Degradation Properties of Molten Alkali Nitrates: LiNO3, NaNO3, KNO3, and Binary NaNO3-KNO3

Science.gov (United States)

Mohammad, Mehedi Bin; Brooks, Geoffrey Alan; Rhamdhani, Muhammad Akbar

2018-06-01

A simultaneous thermal analyzer (STA) was used to observe the transition and degradation events of LiNO3, NaNO3, KNO3, and binary NaNO3-KNO3 salts for potential use as phase change materials (PCMs) and heat transfer fluid (HTF). Samples were heated from 50 °C to 800 °C at 10 °C/min scanning rate in three atmospheres (argon, air, and oxygen) using an STA to observe decomposition behavior. Thermal stability increased for all salts at high partial pressure of O2 ( P_{{{O}2 }} = 1.0) compared to inert argon ( P_{{{O}2 }} = 0). O2, N2, NO, N2O, and NO2 were main evolved gases during nitrate decomposition. NO and O2 started to evolve at approximately the same temperature after melting, indicating that primary and secondary decomposition reactions were concurrent and overlapping. The solid-solid transition, liquidus and solidus temperatures, heat of transition, heat of melting, and heat of solidification were obtained at various heating-cooling rates (1, 2, 4, 5, 6, 8, 10, and 15 °C/min) using an STA. At all heating-cooling rates, a small gap exists between liquidus and solidus temperatures for all samples due to the salts exhibiting supercooling phenomena. This study showed that the degradation point depends on the blanket atmosphere top of the molten salts and that heating rates have a minor effect on transition events (peaks height, peaks width, and transition enthalpies).

Nitrate removal from water using denitrifier-bacteria immobilized on activated carbon at fluidized-bed reactor

Directory of Open Access Journals (Sweden)

hatam Godini

2012-09-01

Results: The experimental results demonstrated that the over 94% of NO3-N was removed in the 2-3 h retention time, almost no NO2-N accumulated in treated water when the concentration of NO3-N was around 50-100 mg/L in influent. Under the experimental conditions, drinking water quality was achieved at a nitrogen loading lower than 2.4 kgNO3-N•m-3•day-1 with an influent COD/N ratio of 3 if ethanol was used as the carbon source. The denitrification rate increased up to a maximal value of 3.45 kgNO3-N•m-3•day-1 with increasing nitrogen loading rate (4.8 kgNO3-N•m-3•day-1. Conclusion: This study demonstrates that GAC offers favorable attachment sites for bacteria on the surfaces of GAC for Nitrate removal and denitrification of water was carried out in a fluidized bed reactor (FBR using Activated carbon-immobilized cell beads as support carriers.

Termites and large herbivores influence seed removal rates in an African savanna.

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Acanakwo, Erik Francis; Sheil, Douglas; Moe, Stein R

2017-12-01

Seed removal can influence plant community dynamics, composition, and resulting vegetation characteristics. In the African savanna, termites and large herbivores influence vegetation in various ways, likely including indirect effects on seed predators and secondary dispersers. However, the intensity and variation of seed removal rates in African savannas has seldom been studied. We experimentally investigated whether termites and large herbivores were important factors in the mechanisms contributing to observed patterns in tree species composition on and off mounds, in Lake Mburo National Park, Uganda. Within fenced (excluding large herbivores) and unfenced termite mound and adjacent savanna plots, we placed seeds of nine native tree species within small open "cages," accessed by all animals, roofed cages that only allowed access to small vertebrates and invertebrates, and closed cages that permitted access by smaller invertebrates only (5 mm wire mesh). We found that mean seed removal rate was high (up to 87.3% per 3 d). Mound habitats experienced significantly higher removal rates than off-mound habitats. The mean removal rate of native seeds from closed cages was 11.1% per 3 d compared with 19.4% and 23.3% removed per 3 d in the roofed and open cages, respectively. Smaller seeds experienced higher removal rates than larger seeds. Large herbivore exclusion on mounds reduced native seed removal rates by a mean of 8.8% in the open cages, but increased removal rates by 1.7% in the open cages when off-mound habitats were fenced. While removal rates from open cages were higher on active mounds (30.9%) than on inactive mounds (26.7%), the removal rates from closed cages were lower on active vs. inactive mounds (6.1% vs. 11.6%, respectively). Thus, we conclude that large herbivores and Macrotermes mounds influence seed removal rates, though these effects appear indirect. © 2017 by the Ecological Society of America.

High-rate nitrogen removal from waste brine by marine anammox bacteria in a pilot-scale UASB reactor.

Science.gov (United States)

Yokota, Nobuyuki; Watanabe, Yasutsugu; Tokutomi, Takaaki; Kiyokawa, Tomohiro; Hori, Tomoyuki; Ikeda, Daisuke; Song, Kang; Hosomi, Masaaki; Terada, Akihiko

2018-02-01

The goal of this study was to develop a startup strategy for a high-rate anaerobic ammonium oxidation (anammox) reactor to treat waste brine with high concentrations of ammonium from a natural gas plant. An upflow anaerobic sludge blanket (UASB) anammox reactor with an effective volume of 294 L was fed continuously with waste brine with a salinity of 3% and a NH 4 + concentration of 180 mg-N/L, as well as a NaNO 2 solution. By inoculating a methanogenic granular biomass as a biomass carrier, the reactor attained the maximum volumetric nitrogen removal rate (NRR) of 10.7 kg-N/m 3 /day on day 209, which was 1.7 times higher than the highest reported NRR for wastewater of comparable salinity. High-throughput sequencing of 16S rRNA gene amplicons revealed that Candidatus Scalindua wagneri was enriched successfully in granules in the UASB, and it replaced Methanosaeta and became dominant in the granule. The inhibitory effect of NO 2 - on the anammox reaction in the granules was assessed by a 15 N tracer method, and the results showed that anammox activity was maintained at 60% after exposure to 300 mg-N/L of NO 2 - for 24 h. Compared with previous studies of the susceptibilities of Candidatus Brocadia and Candidatus Kuenenia to NO 2 - , the enriched marine anammox bacteria were proven to have comparable or even higher tolerances for high NO 2 - concentrations after a long exposure.

SURGICAL REMOVAL OF EPIRETINAL MEMBRANE WITH AND WITHOUT REMOVAL OF INTERNAL LIMITING MEMBRANE: Comparative Study of Visual Acuity, Features of Optical Coherence Tomography, and Recurrence Rate.

Science.gov (United States)

De Novelli, Fernando J; Goldbaum, Mauro; Monteiro, Mario L R; Bom Aggio, Fabio; Takahashi, Walter Y

2017-12-05

To study and compare visual acuity, foveal thickness, outer limiting layer, ellipsoid zone, and recurrence rate in patients undergoing removal of the epiretinal membrane with and without the removal of the internal limiting membrane (ILM). Sixty-three patients who had the epiretinal membrane removed by a single surgeon were randomly assigned into 2 groups: Group 1 without additional removal of the ILM and Group 2 with removal of the ILM. Patients were followed up and evaluated at the first month, third month, and sixth month, postoperatively. Patients from both groups had a gradual improvement in their vision over time. There was no significant difference in the improvement in visual acuity between the two groups. About tomographic assessment of alterations, no significant differences were found between the groups; however, Group 1 had a higher relapse rate (17%) compared with Group 2 (3.6%) (P = 0.09). Epiretinal membrane removal with and without ILM peeling shows similar functional and anatomical improvements, but the group in which the ILM was not removed seemed to have a higher recurrence rate.

Graphene and g-C3N4 based photocatalysts for NOx removal: A review

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Nikokavoura, Aspasia; Trapalis, Christos

2018-02-01

NOx liberated into atmosphere from automobile exhausts and fossil fuel combustion, comprise the major air pollutants. They are responsible for serious environmental problems such as acid rain, ozone accumulation, haze and photochemical smog. Besides they contribute to the deterioration of human health by causing decrease of the lung function and respiratory problems. The application of photocatalytic methods in order to mitigate the presence of NOx in the atmosphere is preferable as they are environmentally friendly, mild and low cost. Therefore, in this review, the photocatalytic activity of g-C3N4 and graphene based composites towards NOx removal was discussed. NOx oxidation to non volatile nitrates on the surface of graphene and g-C3N4 based photocatalysts has attracted much interest during the last years due to their structures with unique features such as large specific surface area, thermal and chemical stability and enhanced visible light utilization. The formation of 2D-2D intimate heterojunctions between graphene or g-C3N4 and other components ensures the enhanced charge transfer, lifetime of electron/hole pairs and thus photocatalytic activity. The increased visible light harvesting also contributes to their usefulness as effective photocatalytic materials. In the present work, the advantages of these novel photocatalysts and the differences/similarities between them were exhaustively highlighted. The role of graphene as catalyst promoter, electron reservoir, support and photosensitizer in its photocatalytic composites was emphasized. The effect of g-C3N4 doping and copolymerization with metals/semiconductors on its photocatalytic activity towards NOx oxidation was thoroughly discussed. Besides, the preparation methods, photocatalytic efficiencies, type of irradiation, utilization of appropriate cocatalysts, and reaction mechanisms during the photocatalytic NOx removal by graphene and g-C3N4 composies, were summarized. It was demonstrated that in the vast

NO/sub x/ removal facility: MON process

Energy Technology Data Exchange (ETDEWEB)

Fukuda, Y

1974-05-01

A newly developed process for nitrogen oxides removal is described. The MON process, named for Mitsubishi Kizoku, Okabe of Tohoku Univ., and Nippon Kagaku, uses potassium permanganate as an oxidizing agent. Potassium permanganate in alkaline solution converts nitric oxide into nitrate and nitrogen dioxide into nitric acid. The resulting MnO/sub 2/ is easily filtered and recovered as material for the manufacturing of KMnO/sub 4/. Contrary to the conventional methods, the NO/sub x/ conversion rate increases with increasing temperature. Test results at a pilot plant showed that NO/sub x/ was reduced from 570 ppM (nitric oxide 520 ppM) to 27 ppM (mostly NO) at 97 to 98 percent conversion. Another advantage of the process is that other acidic gases such as sulfur dioxide are also removed.

Removal kinetics for gaseous NO and SO2by an aqueous NaClO2solution mist in a wet electrostatic precipitator

KAUST Repository

Park, Hyun-Woo

2016-07-26

Removal kinetics for NO and SO2 by NaClO2 solution mist were investigated in a wet electrostatic precipitator. By varying the molar concentrations of NO, SO2, and NaClO2, the removal rates of NO and SO2 confirmed to range from 34.8 to 72.9 mmol/m3 s and 36.6 to 84.7 mmol/m3 s, respectively, at a fixed gas residence time of 0.25 s. The rate coefficients of NO and SO2 were calculated to be 0.679 (mmol/m3)−0.33 s−1 and 1.401 (mmol/m3)−0.1 s−1 based on the rates of the individual removal of NO and SO2. Simultaneous removal of NO and SO2 investigated after the evaluation of removal rates for their individual treatment was performed. At a short gas residence time, SO2 gas removed more quickly by a mist of NaClO2 solution than NO gas in simultaneous removal experiments. This is because SO2 gas, which has a relatively high solubility in solution, was absorbed more rapidly at the gas–liquid interface than NO gas. NO and SO2 gases were absorbed as nitrite (Formula presented.) and sulfite (Formula presented.) ions, respectively, by the NaClO2 solution mist at the gas–liquid interface. Then, (Formula presented.) and (Formula presented.) were oxidized to nitrate (Formula presented.) and sulfate (Formula presented.), respectively, by reactions with (Formula presented.), ClO2, HClO, and ClO in the liquid phase. © 2016 Informa UK Limited, trading as Taylor & Francis Group

Effects of anionic surfactant on n-hexane removal in biofilters.

Science.gov (United States)

Cheng, Yan; He, Huijun; Yang, Chunping; Yan, Zhou; Zeng, Guangming; Qian, Hui

2016-05-01

The biodegradability of three anion surfactants by biofilm microorganisms and the toxicity of the most readily biodegradable surfactant to biofilm microorganisms were examined using batch experiments, and the optimal concentration of SDS for enhanced removal of hexane was investigated using two biotrickling filters (BTFs) for comparison. Results showed that SDS could be biodegraded by microorganisms, and its toxicity to microorganisms within the experimental range was negligible. The best concentration of SDS in biofiltration of n-hexane was 0.1 CMC and the elimination capacity (EC) of 50.4 g m(-3) h(-1) was achieved at a fixed loading rate (LR) of 72 g m(-3) h(-1). When an inlet concentration of n-hexane increased from 600 to 850 mg m(-3), the removal efficiency (RE) decreased from 67% to 41% by BTF2 (with SDS) and from 52% to 42% by BTF1 (without SDS). SDS could enhance hexane removal from 43% (BTF1) to 60% (BTF2) at gas empty-bed residence time (EBRT) of 7.5 s and an inlet concentration of 200 mg m(-3). Copyright © 2016. Published by Elsevier Ltd.

Comparison of residual NAPL source removal techniques in 3D metric scale experiments

Science.gov (United States)

Atteia, O.; Jousse, F.; Cohen, G.; Höhener, P.

2017-07-01

This study compared four treatment techniques for the removal of a toluene/n-decane as NAPL (Non Aqueous Phase Liquid) phase mixture in identical 1 cubic meter tanks filled with different kind of sand. These four treatment techniques were: oxidation with persulfate, surfactant washing with Tween80®, sparging with air followed by ozone, and thermal treatment at 80 °C. The sources were made with three lenses of 26 × 26 × 6.5 cm, one having a hydraulic conductivity similar to the whole tank and the two others a value 10 times smaller. The four techniques were studied after conditioning the tanks with tap water during approximately 80 days. The persulfate treatment tests showed average removal of the contaminants but significant flux decrease if density effects are considered. Surfactant flushing did not show a highly significant increase of the flux of toluene but allowed an increased removal rate that could lead to an almost complete removal with longer treatment time. Sparging removed a significant amount but suggests that air was passing through localized gas channels and that the removal was stagnating after removing half of the contamination. Thermal treatment reached 100% removal after the target temperature of 80 °C was kept during more than 10 d. The experiments emphasized the generation of a high-spatial heterogeneity in NAPL content. For all the treatments the overall removal was similar for both n-decane and toluene, suggesting that toluene was removed rapidly and n-decane more slowly in some zones, while no removal existed in other zones. The oxidation and surfactant results were also analyzed for the relation between contaminant fluxes at the outlet and mass removal. For the first time, this approach clearly allowed the differentiation of the treatments. As a conclusion, experiments showed that the most important differences between the tested treatment techniques were not the global mass removal rates but the time required to reach 99% decrease in

Electrokinetic removal of Ca(NO3)2 from bricks to avoid salt induced decay

DEFF Research Database (Denmark)

Ottosen, Lisbeth M.; Rörig-Dalgaard, Inge

2007-01-01

Salt-induced decay of masonry is a serious threat to our cultural heritage. In buildings near agricultural land or stables the masonry may suffer seriously from salt-induced decay from nitrates. It was investigated in laboratory scale with a single brick if Ca(NO$-3$/) $-2$/ could be removed by e...

Simultaneous removal and evaluation of organic substrates and NH3-N by a novel combined process in treating chemical synthesis-based pharmaceutical wastewater

International Nuclear Information System (INIS)

Chen, Zhaobo; Wang, Hongcheng; Ren, Nanqi; Cui, Minhua; Nie, Shukai; Hu, Dongxue

2011-01-01

Highlights: ► We research a novel combined process to treat chemical synthesis-based pharmaceutical wastewater. ► The mechanism of amoxicillin verifies that the biodegradation, adsorption, hydrolysis and unknown mechanism were able to remove amoxicillin from wastewater. ► In this study demonstrates that biodegradation is the major factor for removal mechanism at work for amoxicillin. ► Mathematical statistic methods were employed to evaluate the performance of the WWTP. - Abstract: A full-scale novel combined anaerobic/micro-aerobic and two-stage aerobic biological process is used for the treatment of an actual chemical synthesis-based pharmaceutical wastewater containing amoxicillin. The anaerobic system is an up-flow anaerobic sludge blanket (UASB), the micro-aerobic system is a novel micro-aerobic hydrolysis acidification reactor (NHAR) and the two-stage aerobic process comprised cyclic activated sludge system (CASS) and biological contact oxidation tank (BCOT). The influent wastewater was high in COD, NH 3 -N varying daily 4016–13,093 mg-COD L −1 and 156.4–650.2 mg-NH 3 -N L −1 , amoxicillin varying weekly between 69.1 and 105.4 mg-amoxicillin L −1 , respectively; Almost all the COD, NH 3 -N, amoxicillin were removed by the biological combined system, with removal percentages 97%, 93.4% and 97.2%, respectively, leaving around 104 mg-COD L −1 , 9.4 mg-NH 3 -N L −1 and 2.6 ± 0.8 mg-amoxicillin L −1 in the final clarifier effluent. The performance evaluation of the wastewater treatment plant (WWTP) by mathematical statistic methods shown that at most of time effluent can meet the higher treatment discharge standard. In addition, the fate of amoxicillin in the full-scale WWTP and the amoxicillin removal rate of each different removal routes in UASB, NHAR, CASS, BCOT and final clarifier processes are investigated in this paper. The results show that biodegradation, adsorption and hydrolysis are the major mechanisms for amoxicillin removal.

Effects of NH3 Flow Rate During AlGaN Barrier Layer Growth on the Material Properties of AlGaN/GaN HEMT Heterostructure

Science.gov (United States)

Lumbantoruan, Franky J.; Wong, Yuen-Yee; Huang, Wei-Ching; Yu, Hung-Wei; Chang, Edward-Yi

2017-10-01

NH3 flow rate during AlGaN barrier layer growth not only affects the growth efficiency and surface morphology as a result of parasitic reactions but also influences the concentration of carbon impurity in the AlGaN barrier. Carbon, which decomposes from metal precursors, plays a role in electron compensation for AlGaN/GaN HEMT. No 2-dimensional electron gas (2-DEG) was detected in the AlGaN/GaN structure if grown with 0.5 slm of NH3 due to the presence of higher carbon impurity (2.6 × 1019 cm-2). When the NH3 flow rate increased to 6.0 slm, the carbon impurity reduced to 2.10 × 1018 atom cm-3 and the 2 DEG electron density recovered to 9.57 × 1012 cm-2.

Enhanced NO2 abatement by alkaline-earth modified g-C3N4 nanocomposites for efficient air purification

Science.gov (United States)

Papailias, Ilias; Todorova, Nadia; Giannakopoulou, Tatiana; Karapati, Sofia; Boukos, Nikos; Dimotikali, Dimitra; Trapalis, Christos

2018-02-01

The emission of nitrogen dioxide (NO2) is a major problem encountered in photocatalytic NOx removal for air purification. Although the oxidation of nitric oxide (NO) has been extensively studied, the elimination of NO2 byproduct is still in preliminary stage. In this work, alkaline-earth modified graphitic carbon nitride (g-C3N4) is proposed for efficient NOx removal by minimizing the emission of NO2 during the NO oxidation process. The novel photocatalysts were synthesized by annealing mixtures of melamine and various alkaline-earth acetates (magnesium, calcium and barium acetate) at 550 °C for 3 h. The specific surface area of the photocatalysts varied between 4.65 and 11.81 m2/g. The formation of MgO, CaCO3 and BaCO3 was demonstrated by XPS and FT-IR analyses. The initial concentration of each alkaline-earth precursor was 5 and 10 wt%, while the final metal concentration in the nanocomposites was in the range of 7.19-22.39 wt%. The modified photocatalysts showed slightly reduced NO oxidation ability. However, the overall air quality was significantly improved by restraining the NO2 emission. The results were related to the basic character of the nanocomposites due to the presence of alkaline-earths and their enhanced NO2 adsorption capability.

Nitrogen removal and nitrate leaching for two perennial, sod-based forage systems receiving dairy effluent.

Science.gov (United States)

Woodard, Kenneth R; French, Edwin C; Sweat, Lewin A; Graetz, Donald A; Sollenberger, Lynn E; Macoon, Bisoondat; Portier, Kenneth M; Rymph, Stuart J; Wade, Brett L; Prine, Gordon M; Van Horn, Harold H

2003-01-01

In northern Florida, year-round forage systems are used in dairy effluent sprayfields to reduce nitrate leaching. Our purpose was to quantify forage N removal and monitor nitrate N (NO3(-)-N) concentration below the rooting zone for two perennial, sod-based, triple-cropping systems over four 12-mo cycles (1996-2000). The soil is an excessively drained Kershaw sand (thermic, uncoated Typic Quartzip-samment). Effluent N rates were 500, 690, and 910 kg ha(-1) per cycle. Differences in N removal between a corn (Zea mays L.)-bermudagrass (Cynodon spp.)-rye (Secale cereale L.) system (CBR) and corn-perennial peanut (Arachis glabrata Benth.)-rye system (CPR) were primarily related to the performance of the perennial forages. Nitrogen removal of corn (125-170 kg ha(-1)) and rye (62-90 kg ha(-1)) was relatively stable between systems and among cycles. The greatest N removal was measured for CBR in the first cycle (408 kg ha(-1)), with the bermudagrass removing an average of 191 kg N ha(-1). In later cycles, N removal for bermudagrass declined because dry matter (DM) yield declined. Yield and N removal of perennial peanut increased over the four cycles. Nitrate N concentrations below the rooting zone were lower for CBR than CPR in the first two cycles, but differences were inconsistent in the latter two. The CBR system maintained low NO3(-)-N leaching in the first cycle when the bermudagrass was the most productive; however, it was not a sustainable system for long-term prevention of NO3(-)-N leaching due to declining bermudagrass yield in subsequent cycles. For CPR, effluent N rates > or = 500 kg ha(-1) yr(-1) have the potential to negatively affect ground water quality.

Simultaneous removal and evaluation of organic substrates and NH{sub 3}-N by a novel combined process in treating chemical synthesis-based pharmaceutical wastewater

Energy Technology Data Exchange (ETDEWEB)

Chen, Zhaobo [School of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001 (China); State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Wang, Hongcheng [School of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001 (China); Ren, Nanqi, E-mail: rnq@hit.edu.cn [State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Cui, Minhua; Nie, Shukai; Hu, Dongxue [School of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001 (China)

2011-12-15

Highlights: Black-Right-Pointing-Pointer We research a novel combined process to treat chemical synthesis-based pharmaceutical wastewater. Black-Right-Pointing-Pointer The mechanism of amoxicillin verifies that the biodegradation, adsorption, hydrolysis and unknown mechanism were able to remove amoxicillin from wastewater. Black-Right-Pointing-Pointer In this study demonstrates that biodegradation is the major factor for removal mechanism at work for amoxicillin. Black-Right-Pointing-Pointer Mathematical statistic methods were employed to evaluate the performance of the WWTP. - Abstract: A full-scale novel combined anaerobic/micro-aerobic and two-stage aerobic biological process is used for the treatment of an actual chemical synthesis-based pharmaceutical wastewater containing amoxicillin. The anaerobic system is an up-flow anaerobic sludge blanket (UASB), the micro-aerobic system is a novel micro-aerobic hydrolysis acidification reactor (NHAR) and the two-stage aerobic process comprised cyclic activated sludge system (CASS) and biological contact oxidation tank (BCOT). The influent wastewater was high in COD, NH{sub 3}-N varying daily 4016-13,093 mg-COD L{sup -1} and 156.4-650.2 mg-NH{sub 3}-N L{sup -1}, amoxicillin varying weekly between 69.1 and 105.4 mg-amoxicillin L{sup -1}, respectively; Almost all the COD, NH{sub 3}-N, amoxicillin were removed by the biological combined system, with removal percentages 97%, 93.4% and 97.2%, respectively, leaving around 104 mg-COD L{sup -1}, 9.4 mg-NH{sub 3}-N L{sup -1} and 2.6 {+-} 0.8 mg-amoxicillin L{sup -1} in the final clarifier effluent. The performance evaluation of the wastewater treatment plant (WWTP) by mathematical statistic methods shown that at most of time effluent can meet the higher treatment discharge standard. In addition, the fate of amoxicillin in the full-scale WWTP and the amoxicillin removal rate of each different removal routes in UASB, NHAR, CASS, BCOT and final clarifier processes are investigated

Rate constants of the equilibrium reactions SO⨪4 + HNO3 ⇄ HSO-4 + NO3 and SO⨪4 + NO-3 ⇄ SO2-4 + NO3

DEFF Research Database (Denmark)

Løgager, T.; Sehested, K.; Holcman, J.

1993-01-01

Rate constants of the following equilibrium reactions were determined by pulse radiolysis at high solute concentrations: SO4.- + HNO, half arrow right over half arrow left HSO4- + NO3. [k(f) = (2.7 +/- 0.5) x 10(6) M-1 s-1, k(r) = (5.6 +/- 1.0) x 10(3) M-1 s-1] and SO4.- + NO3- half arrow right...

Production of 15N-enriched nitric acid (H15NO3

Directory of Open Access Journals (Sweden)

C. R. Sant Ana Filho

2008-12-01

Full Text Available Techniques that employ 15N have proved to be an important tool in many areas of the agronomic and biomedical sciences. Nevertheless, their use is limited by methodological difficulties and by the price of compounds in the international market. Nitric compounds (15NO3- have attracted the interest of researchers. However, these compounds are not currently produced in Brazil. Thus, in the present work H15NO3 was obtained from the oxidation of anhydrous 15NH3. The method we used differs from the industrial process in that the absorption tower is replaced with a polytetrafluoroethylene-lined, stainless-steel hydration reactor. The process output was evaluated based on the following parameters: reaction temperature; ratio of reagents; pressure and flow of 15NH3(g through the catalyst (Pt/Rh. The results showed that, at the best conditions (500 ºC; 50 % excess O2; 0.4 MPa; and 3.39 g.min-1 of 15NH3, a conversion percentage (N-15NH3 to N-15NO3- of 62.2 %, an overall nitrogen balance (N-15NH3 + N-15NO3- of 86.8 %, and purity higher than 99 % could be obtained.

Hierarchical magnetic petal-like Fe3O4-ZnO@g-C3N4 for removal of sulfamethoxazole, suppression of photocorrosion, by-products identification and toxicity assessment.

Science.gov (United States)

Mirzaei, Amir; Chen, Zhi; Haghighat, Fariborz; Yerushalmi, Laleh

2018-08-01

Herein, a petal-like photocatalyst, Fe 3 O 4 -ZnO@g-C 3 N 4 (FZG) with different g-C 3 N 4 to ZnO ratios was synthesized with hierarchical structure. The FZG1 photocatalyst, having the weight ratio of 1:1 for the initial urea and Fe 3 O 4 -ZnO (Fe-ZnO), presented the highest sulfamethoxazole (SMX) degradation rate of 0.0351 (min -1 ), which was 2.6 times higher than that of pristine ZnO. Besides the facile separation, the performance of photocatalyst was improved due to the function of iron oxide as an electron acceptor that reduced the electron/hole recombination rate. The coating of g-C 3 N 4 on the Fe-ZnO surface not only acted as a protective layer for ZnO against photocorrosion, but it also enhanced the photocatalytic activity of the catalyst for SMX degradation through the heterojunction mechanism. By using the FZG1 photocatalyst, 95% SMX removal was obtained after 90 min reaction, while 47% COD and 30% TOC removal were achieved after 60 min treatment under a low energy-consuming UV lamp (10 W). Moreover, a substantial reduction in the solution toxicity was shown after the treatment, as compared with the SMX solution before treatment. The LC-HR-MS/MS analysis results showed that the concentration of most detected by-products produced after 90 min reaction by FZG1 was considerably lower than those obtained using other synthesized photocatalysts. By performing radical scavenging experiments, OH ° radical was found to be the major reactive species. The FZG1 photocatalyst also displayed excellent reusability in five cycles and the leaching of zinc and iron ions was reduced by 54% and ∼100%, respectively, after coating Fe-ZnO with g-C 3 N 4 . Copyright © 2018 Elsevier Ltd. All rights reserved.

Influences of seasons, N/P ratios and chemical compounds on phosphorus removal performance in algal pond combined with constructed wetlands.

Science.gov (United States)

Zhimiao, Zhao; Xinshan, Song; Yanping, Xiao; Yufeng, Zhao; Zhijie, Gong; Fanda, Lin; Yi, Ding; Wei, Wang; Tianling, Qin

2016-12-15

Nitrogen (N) and phosphorous (P) are main contaminants and P removal was restrained by several factors: season, N/P, and chemical compounds (CCs) in water ecosystems. In this paper, two algal ponds combined with constructed wetlands were built to increase the removal performance. Different hydraulic retention time (HRT), different N/P and chemical compounds were chosen to investigate the influences of the above factors on the contaminant removal performance. The optimum phosphorus removal rate was 69.74% under the nitrogen removal of 92.85% in influent containing PO 4 3- after 3-day HRT in algal pond combined with constructed wetlands. The investigation results indicated that these factors improved the nutrient removal efficiencies. Seasonal influence on the removal performance can be avoided by choosing the optimal HRT length of 3days. The higher N/P at 60 can improve the phosphorus removal and the lower N/P at 15 showed the stronger synergistic effect between phosphorus and nitrogen removals. Compared with PO 3 - and P 2 O 7 4- in influent, PO 4 3- affected phosphorus removal more significantly. The better linear fitting between organic phosphorus removal and nitrogen removal in influent contained P 2 O 7 4- was found. Algae can absorb nutrients for growth, and oxygen release, microbial activity intensification and microbial carbon replenishment induced by algae will improve the performance. The study suggested that the control of HRTs, N/Ps, CCs, and algae might be an effective way to improve wastewater treatment performance. Copyright © 2016 Elsevier B.V. All rights reserved.

Rate-based modelling of combined SO2 removal and NH3 recycling integrated with an aqueous NH3-based CO2 capture process

International Nuclear Information System (INIS)

Li, Kangkang; Yu, Hai; Qi, Guojie; Feron, Paul; Tade, Moses; Yu, Jingwen; Wang, Shujuan

2015-01-01

Highlights: • A rigorous, rate-based model for an NH 3 –CO 2 –SO 2 –H 2 O system was developed. • Model predictions are in good agreement with pilot plant results. • >99.9% of SO 2 was captured and >99.9% of slipped ammonia was reused. • The process is highly adaptable to the variations of SO 2 /NH 3 level, temperatures. - Abstract: To reduce the costs of controlling emissions from coal-fired power stations, we propose an advanced and effective process of combined SO 2 removal and NH 3 recycling, which can be integrated with the aqueous NH 3 -based CO 2 capture process to simultaneously achieve SO 2 and CO 2 removal, NH 3 recycling and flue gas cooling in one process. A rigorous, rate-based model for an NH 3 –CO 2 –SO 2 –H 2 O system was developed and used to simulate the proposed process. The model was thermodynamically and kinetically validated by experimental results from the open literature and pilot-plant trials, respectively. Under typical flue gas conditions, the proposed process has SO 2 removal and NH 3 reuse efficiencies of >99.9%. The process is strongly adaptable to different scenarios such as high SO 2 levels in flue gas, high NH 3 levels from the CO 2 absorber and high flue gas temperatures, and has a low energy requirement. Because the process simplifies flue gas desulphurisation and resolves the problems of NH 3 loss and SO 2 removal, it could significantly reduce the cost of CO 2 and SO 2 capture by aqueous NH 3

Simultaneous removal of SO2, NO and Hg0 from flue gas by ferrate (VI) solution

International Nuclear Information System (INIS)

Zhao, Yi; Han, Yinghui; Guo, Tianxiang; Ma, Tianzhong

2014-01-01

Simultaneously removing SO 2 , NO and Hg 0 from flue gas was examined by ferrate (VI) solution at a bubbling reactor. The removal efficiencies of 100% for SO 2 , 64.8% for NO and 81.4% for Hg 0 were achieved respectively, under the optimum experimental conditions, in which concentration of ferrate (VI) solution was 0.25 mmol/L, solution pH was 8.0, flue gas flow rate was 1 L/min and reaction temperature was 320 K. Based on the discussions of the ferrate (VI) solution characteristics, the comparisons of the standard electrode potential (E 0 ) of ferrate (VI) solution with E 0 values of reactant, and the analysis of the reaction products, a mechanism of simultaneous removal was proposed. In the process of simultaneous removal, FeO 4 2− and HFeO 4 − as the dominant species of ferrate (VI), could rapidly oxidize SO 2 , NO, and Hg 0 into SO 4 2− , NO 3 − and Hg 2+ . - Highlights: • Prepared ferrate (VI) absorbent has excellent property of removing SO 2 , NO and Hg 0 . • 100% of SO 2 , 63.8% of NO and 83.6% of Hg 0 were simultaneously removed. • The simultaneous removal mechanism of SO 2 , NO and Hg 0 was proposed

Microbial electricity driven anoxic ammonium removal.

Science.gov (United States)

Vilajeliu-Pons, Anna; Koch, Christin; Balaguer, Maria D; Colprim, Jesús; Harnisch, Falk; Puig, Sebastià

2018-03-01

Removal of nitrogen, mainly in form of ammonium (NH 4 + ), in wastewater treatment plants (WWTPs) is a highly energy demanding process, mainly due to aeration. It causes costs of about half a million Euros per year in an average European WWTP. Alternative, more economical technologies for the removal of nitrogen compounds from wastewater are required. This study proves the complete anoxic conversion of ammonium (NH 4 + ) to dinitrogen gas (N 2 ) in continuously operated bioelectrochemical systems at the litre-scale. The removal rate is comparable to conventional WWTPs with 35 ± 10 g N m -3 d -1 with low accumulation of NO 2 - , NO 3 - , N 2 O. In contrast to classical aerobic nitrification, the energy consumption is considerable lower (1.16 ± 0.21 kWh kg -1 N, being more than 35 times less than for the conventional wastewater treatment). Biotic and abiotic control experiments confirmed that the anoxic nitrification was an electrochemical biological process mainly performed by Nitrosomonas with hydroxylamine as the main substrate (mid-point potential, E ox  = +0.67 ± 0.08 V vs. SHE). This article proves the technical feasibility and reduction of costs for ammonium removal from wastewater, investigates the underlying mechanisms and discusses future engineering needs. Copyright © 2017 Elsevier Ltd. All rights reserved.

Communication: Equilibrium rate coefficients from atomistic simulations: The O(3P) + NO(2Π) → O2(X3Σg−) + N(4S) reaction at temperatures relevant to the hypersonic flight regime

International Nuclear Information System (INIS)

Castro-Palacio, Juan Carlos; Bemish, Raymond J.; Meuwly, Markus

2015-01-01

The O( 3 P) + NO( 2 Π) → O 2 (X 3 Σ g − ) + N( 4 S) reaction is among the N- and O- involving reactions that dominate the energetics of the reactive air flow around spacecraft during hypersonic atmospheric re-entry. In this regime, the temperature in the bow shock typically ranges from 1000 to 20 000 K. The forward and reverse rate coefficients for this reaction derived directly from trajectory calculations over this range of temperature are reported in this letter. Results compare well with the established equilibrium constants for the same reaction from thermodynamic quantities derived from spectroscopy in the gas phase which paves the way for large-scale in silico investigations of equilibrium rates under extreme conditions

Communication: Equilibrium rate coefficients from atomistic simulations: The O((3)P) + NO((2)Π) → O2(X(3)Σg(-)) + N((4)S) reaction at temperatures relevant to the hypersonic flight regime.

Science.gov (United States)

Castro-Palacio, Juan Carlos; Bemish, Raymond J; Meuwly, Markus

2015-03-07

The O((3)P) + NO((2)Π) → O2(X(3)Σg(-)) + N((4)S) reaction is among the N- and O- involving reactions that dominate the energetics of the reactive air flow around spacecraft during hypersonic atmospheric re-entry. In this regime, the temperature in the bow shock typically ranges from 1000 to 20,000 K. The forward and reverse rate coefficients for this reaction derived directly from trajectory calculations over this range of temperature are reported in this letter. Results compare well with the established equilibrium constants for the same reaction from thermodynamic quantities derived from spectroscopy in the gas phase which paves the way for large-scale in silico investigations of equilibrium rates under extreme conditions.

Readiness evaluation report -- High-exposure rate hardware removal resumption of activities

International Nuclear Information System (INIS)

Volkman, C.L.

1996-11-01

In August 1996, N Basin Project Management proactively ceased activities in the N Basin after noting several radiological control anomalies occurring during the performance of the high exposure rate hardware removal activity. The HERH is one of several activities that will be accomplished to complete deactivation of N Basin. Three project critiques were performed to identify causes and several corrective actions were identified. To ensure the true causes of the events were identified the N Basin Project Manager requested that a root cause analysis be performed for the events covered by the three critiques. The intent was to identify recurring events and evaluate the effectiveness of corrective action implementation. These three review elements were used by the project to develop a corrective action plan (CAP) which consisted of both project unique and programmatic items. The N Basin Project is using this BHI Readiness Evaluation (RE) process as a mechanism to independently verify that corrective actions identified from the CAP have been completed and that no changes have been made during the stand down that affect the resumption of the HERH activities. A readiness evaluation (RE) plan (Attachment 3) was prepared. The completed Readiness Evaluation Records which documents the results of the team member evaluations are in attachment 1. The independent readiness evaluation team identified 5 deficiencies of which two are post startup and three are pre startup. All deficiencies are in the area of training. These findings are explained in detail in Attachment 2

Removal kinetics for gaseous NO and SO2by an aqueous NaClO2solution mist in a wet electrostatic precipitator

KAUST Repository

Park, Hyun-Woo; Park, Dong-Wha

2016-01-01

Removal kinetics for NO and SO2 by NaClO2 solution mist were investigated in a wet electrostatic precipitator. By varying the molar concentrations of NO, SO2, and NaClO2, the removal rates of NO and SO2 confirmed to range from 34.8 to 72.9 mmol/m3

Near-ultraviolet removal rates for subgingival dental calculus at different irradiation angles

Science.gov (United States)

Schoenly, Joshua E.; Seka, Wolf D.; Rechmann, Peter

2011-07-01

The laser ablation rate of subgingival dental calculus irradiated at a 400-nm-wavelength, 7.4-mJ pulse energy, and 85- and 20-deg irradiation angles is measured using laser triangulation. Three-dimensional images taken before and after irradiation create a removal map with 6-μm axial resolution. Fifteen human teeth with subgingival calculus are irradiated in vitro under a cooling water spray with an ~300-μm-diam, tenth-order super-Gaussian beam. The average subgingival calculus removal rates for irradiation at 85 and 20 deg are 11.1+/-3.6 and 11.5+/-5.9 μm/pulse, respectively, for depth removal and 4.5+/-1.7×105 and 4.8+/-2.3×105 μm3/pulse, respectively, for volume removal. The ablation rate is constant at each irradiation site but varies between sites because of the large differences in the physical and optical properties of calculus. Comparison of the average depth- and volume-removal rates does not reveal any dependence on the irradiation angle and is likely due to the surface topology of subgingival calculus samples that overshadows any expected angular dependence.

Nitrate removal performance of Diaphorobacter nitroreducens using biodegradable plastics as the source of reducing power

Energy Technology Data Exchange (ETDEWEB)

Khan, S. T. [Department of Environmental and Life Sciences, Toyohashi University of Technology, Toyohashi 441-8580, Japan and Department of Zoology, College of Science, King Saud University, Riyadh (Saudi Arabia); Nagao, Y. [Department of Environmental and Life Sciences, Toyohashi University of Technology, Toyohashi 441-8580 (Japan); Hiraishi, A., E-mail: hiraishi@ens.tut.ac.jp [Department of Environmental and Life Sciences, Toyohashi University of Technology, Toyohashi 441-8580, Japan and Electronics-Inspired Interdisciplinary Research Institute (EIIRIS), Toyohashi University of Technology, Toyohashi 441-8580 (Japan)

2015-02-27

Strain NA10B{sup T} and other two strains of the denitrifying betaproteobacterium Diaphorobacter nitroreducens were studied for the performance of solid-phase denitrification (SPD) using poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) and some other biodegradable plastics as the source of reducing power in wastewater treatment. Sequencing-batch SPD reactors with these organisms and PHBV granules or flakes as the substrate exhibited good nitrate removal performance. Vial tests using cultures from these parent reactors showed higher nitrate removal rates with PHBV granules (ca. 20 mg-NO{sub 3}{sup −}‐N g{sup −1} [dry wt cells] h{sup −1}) than with PHBV pellets and flakes. In continuous-flow SPD reactors using strain NA10B{sup T} and PHBV flakes, nitrate was not detected even at a loading rate of 21 mg-NO{sub 3}{sup −}‐N L{sup −1} h{sup −1}. This corresponded to a nitrate removal rate of 47 mg-NO{sub 3}{sup −}‐N g{sup −1} (dry wt cells) h{sup −1}. In the continuous-flow reactor, the transcription level of the phaZ gene, coding for PHB depolymerase, decreased with time, while that of the nosZ gene, involved in denitrificaiton, was relatively constant. These results suggest that the bioavailability of soluble metabolites as electron donor and carbon sources increases with time in the continuous-flow SPD process, thereby having much higher nitrate removal rates than the process with fresh PHBV as the substrate.

Nitrate removal in a restored riparian groundwater system: functioning and importance of individual riparian zones

Directory of Open Access Journals (Sweden)

S. Peter

2012-11-01

Full Text Available For the design and the assessment of river restoration projects, it is important to know to what extent the elimination of reactive nitrogen (N can be improved in the riparian groundwater. We investigated the effectiveness of different riparian zones, characterized by a riparian vegetation succession, for nitrate (NO₃⁻ removal from infiltrating river water in a restored and a still channelized section of the river Thur, Switzerland. Functional genes of denitrification (nirS and nosZ were relatively abundant in groundwater from willow bush and mixed forest dominated zones, where oxygen concentrations remained low compared to the main channel and other riparian zones. After flood events, a substantial decline in NO₃⁻ concentration (> 50% was observed in the willow bush zone but not in the other riparian zones closer to the river. In addition, the characteristic enrichment of ¹⁵N and ¹⁸O in the residual NO₃⁻ pool (by up to 22‰ for δ¹⁵N and up to 12‰ for δ¹⁸O provides qualitative evidence that the willow bush and forest zones were sites of active denitrification and, to a lesser extent, NO₃⁻ removal by plant uptake. Particularly in the willow bush zone during a period of water table elevation after a flooding event, substantial input of organic carbon into the groundwater occurred, thereby fostering post-flood denitrification activity that reduced NO₃⁻ concentration with a rate of ~21 μmol N l⁻¹ d⁻¹. Nitrogen removal in the forest zone was not sensitive to flood pulses, and overall NO₃⁻ removal rates were lower (~6 μmol l⁻¹ d⁻¹. Hence, discharge-modulated vegetation–soil–groundwater coupling was found to be a key driver for riparian NO₃⁻ removal. We estimated that

The black rock series supported SCR catalyst for NO x removal.

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Xie, Bin; Luo, Hang; Tang, Qing; Du, Jun; Liu, Zuohua; Tao, Changyuan

2017-09-01

Black rock series (BRS) is of great potential for their plenty of valued oxides which include vanadium, iron, alumina and silica oxides, etc. BRS was used for directly preparing of selective catalytic reduction (SCR) catalyst by modifying its surface texture with SiO 2 -TiO 2 sols and regulating its catalytic active constituents with V 2 O 5 and MoO 3 . Consequently, 90% NO removal ratio was obtained within 300-400 °C over the BRS-based catalyst. The structure and properties of the BRS-based catalyst were characterized by the techniques of N 2 adsorption-desorption, X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), H 2 -temperature programmed reduction (H 2 -TPR), and NH 3 -temperature programmed desorption (NH 3 -TPD). The results revealed that the BRS-based catalyst possesses favorable properties for NO x removal, including highly dispersed active components, abundant surface-adsorbed oxygen O α , well redox property, and numerous Brønsted acid sites. Particularly, the BRS-based catalyst exhibited considerable anti-poisoning performance compared with commercial TiO 2 -based catalyst. The former catalyst shows a NO conversion surpassing 80% from 300 to 400 °C for potassium poisoning, and a durability of SO 2 and H 2 O exceeding 85% at temperatures from 300 to 450 °C.

Efficient Photocatalytic Bilirubin Removal over the Biocompatible Core/Shell P25/g-C3N4 Heterojunctions with Metal-free Exposed Surfaces under Moderate Green Light Irradiation

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Kang, Shifei; Qin, Hengfei; Zhang, Lu; Huang, Yongkui; Bai, Xia; Li, Xi; Sun, Di; Wang, Yangang; Cui, Lifeng

2017-03-01

Highly-monodispersed g-C3N4/TiO2 hybrids with a core/shell structure were synthesized from a simple room temperature impregnation method, in which g-C3N4 was coated through self-assembly on the commercially available Degussa P25 TiO2 nanoparticles. Structural and surface characterizations showed that the presence of g-C3N4 notably affected the light absorption characteristics of TiO2. The g-C3N4/TiO2 heterojunctions with metal-free exposed surfaces were directly used as biocompatible photocatalysts for simulated jaundice phototherapy under low-power green-light irradiation. The photocatalytic activity and stability of g-C3N4/TiO2 were enhanced relative to pure P25 or g-C3N4, which could be ascribed to the effective Z-scheme separation of photo-induced charge carriers in g-C3N4/TiO2 heterojunction. The photoactivity was maximized in the 4 wt.% g-C3N4-coated P25, as the bilirubin removal rate under green light irradiation was more than 5-fold higher than that under the clinically-used blue light without any photocatalyst. This study approves the future applications of the photocatalyst-assisted bilirubin removal in jaundice treatment under moderate green light which is more tolerable by humans.

Removing NDMA (N,N-dimethylnitrosamine) from natural waters

Energy Technology Data Exchange (ETDEWEB)

Mezyk, S P [California State University Long Beach, (United States); Cooper, W J [University of North Carolina at Wilmington, (United States); Bartels, D M [Argonne National Laboratory, (United States)

2003-07-01

Nitrosoamines are ubiquitous in water environments, and are of concern as they are potent carcinogens. In particular, N,N-dimethylnitrosamine (NDMA, (CH{sub 3}){sub 2} NNO) is volatile, and therefore has been detected around factories producing secondary amines or rocket fuel, in areas near industrial plants that use dimethylamine in organic synthesis, and even in foods and beverages that contain nitrite or which have been exposed to nitrous oxides. Various technologies have been suggested for removing trace levels of NDMA contamination from aqueous systems. However, Advanced Oxidation Technologies (AOTs), such as ozone, UV/ozone, and UV/H{sub 2}O{sub 2} , which use oxidation via the hydroxyl radical ({sup .}OH), or heterogeneous catalysis by TiO{sub 2} , sonolysis, or the electron beam process, which produce a mixture of oxidizing {sup .}OH radicals with reducing hydrated electrons (e{sup -}{sub aq} ) and hydrogen atoms ({sup .} H), may also produce unwanted stable products in the treatment. Some of these stable products, such as secondary amines, allow regeneration of NDMA to occur. To ensure that any process applied to NDMA contaminated water occurs efficiently and quantitatively a complete understanding of the chemistry involved under the conditions of use is necessary. This requires mathematical modeling of the process, which in turn needs reaction rate constants and mechanisms. In this study, absolute rate constants at room temperature for the reaction of the hydroxyl radical, hydrated electron, and hydrogen atom with NDMA in water have been determined using electron pulse radiolysis and absorption spectroscopy, (e{sup -}{sub aq} and {sup .}OH) and EPR free induction decay attenuation ({sup .}H) measurements. The specific values of (4.30{+-} 0.12) x 10 8 , (1.41 {+-} 0.02) x 10 10 , and (2.01 {+-} 0.03) x 10{sup 8} M{sup -1} s{sup -1} , respectively, demonstrate that the reductive destruction of this nitrosoamine would be the dominant removal pathway in any

Removing NDMA (N,N-dimethylnitrosamine) from natural waters

International Nuclear Information System (INIS)

Mezyk, S.P.; Cooper, W.J.; Bartels, D.M.

2003-01-01

Nitrosoamines are ubiquitous in water environments, and are of concern as they are potent carcinogens. In particular, N,N-dimethylnitrosamine (NDMA, (CH 3 ) 2 NNO) is volatile, and therefore has been detected around factories producing secondary amines or rocket fuel, in areas near industrial plants that use dimethylamine in organic synthesis, and even in foods and beverages that contain nitrite or which have been exposed to nitrous oxides. Various technologies have been suggested for removing trace levels of NDMA contamination from aqueous systems. However, Advanced Oxidation Technologies (AOTs), such as ozone, UV/ozone, and UV/H 2 O 2 , which use oxidation via the hydroxyl radical ( . OH), or heterogeneous catalysis by TiO 2 , sonolysis, or the electron beam process, which produce a mixture of oxidizing . OH radicals with reducing hydrated electrons (e - aq ) and hydrogen atoms ( . H), may also produce unwanted stable products in the treatment. Some of these stable products, such as secondary amines, allow regeneration of NDMA to occur. To ensure that any process applied to NDMA contaminated water occurs efficiently and quantitatively a complete understanding of the chemistry involved under the conditions of use is necessary. This requires mathematical modeling of the process, which in turn needs reaction rate constants and mechanisms. In this study, absolute rate constants at room temperature for the reaction of the hydroxyl radical, hydrated electron, and hydrogen atom with NDMA in water have been determined using electron pulse radiolysis and absorption spectroscopy, (e - aq and . OH) and EPR free induction decay attenuation ( . H) measurements. The specific values of (4.30± 0.12) x 10 8 , (1.41 ± 0.02) x 10 10 , and (2.01 ± 0.03) x 10 8 M -1 s -1 , respectively, demonstrate that the reductive destruction of this nitrosoamine would be the dominant removal pathway in any remediation process. Based on these data we have begun modeling the large-scale electron

Simultaneous removal of NO and SO2 using vacuum ultraviolet light (VUV)/heat/peroxymonosulfate (PMS).

Science.gov (United States)

Liu, Yangxian; Wang, Yan; Wang, Qian; Pan, Jianfeng; Zhang, Jun

2018-01-01

Simultaneous removal process of SO 2 and NO from flue gas using vacuum ultraviolet light (VUV)/heat/peroxymonosulfate (PMS) in a VUV spraying reactor was proposed. The key influencing factors, active species, reaction products and mechanism of SO 2 and NO simultaneous removal were investigated. The results show that vacuum ultraviolet light (185 nm) achieves the highest NO removal efficiency and yield of and under the same test conditions. NO removal is enhanced at higher PMS concentration, light intensity and oxygen concentration, and is inhibited at higher NO concentration, SO 2 concentration and solution pH. Solution temperature has a double impact on NO removal. CO 2 concentration has no obvious effect on NO removal. and produced from VUV-activation of PMS play a leading role in NO removal. O 3 and ·O produced from VUV-activation of O 2 also play an important role in NO removal. SO 2 achieves complete removal under all experimental conditions due to its very high solubility in water and good reactivity. The highest simultaneous removal efficiency of SO 2 and NO reaches 100% and 91.3%, respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

Nitrogen removal through N cycling from sediments in a constructed coastal marsh as assessed by 15N-isotope dilution.

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Ro, Hee-Myong; Kim, Pan-Gun; Park, Ji-Suk; Yun, Seok-In; Han, Junho

2018-04-01

Constructed coastal marsh regulates land-born nitrogen (N) loadings through salinity-dependent microbial N transformation processes. A hypothesis that salinity predominantly controls N removal in marsh was tested through incubation in a closed system with added- 15 NH 4 + using sediments collected from five sub-marshes in Shihwa marsh, Korea. Time-course patterns of concentrations and 15 N-atom% of soil-N pools were analyzed. Sediments having higher salinity and lower soil organic-C and acid-extractable organic-N exhibited slower rates of N mineralization and immobilization, nitrification, and denitrification. Rates of denitrification were not predicted well by sediment salinity but by its organic-C, indicating heterotrophic denitrification. Denitrification dominated N-loss from this marsh, and nitrogen removal capacity of this marsh was estimated at 337 kg N day -1 (9.9% of the daily N-loadings) considering the current rooting depth of common reeds (1.0 m). We showed that sediment N removal decreases with increasing salinity and can increase with increasing organic-C for heterotrophic denitrification. Copyright © 2018 Elsevier Ltd. All rights reserved.

Impact of exogenous organic carbon on the removal of chemicals of concern in the high rate nitrifying trickling filters.

Science.gov (United States)

Mai, Lei; van den Akker, Ben; Du, Jun; Kookana, Rai S; Fallowfield, Howard

2016-06-01

The application of fixed bed high rate nitrifying trickling filters (NTFs) for the removal of track organic chemicals of concern (CoC) is less well known than their application to nutrient removal in water treatment. Particularly, the effect of exogenous organic carbon substrate (sucrose) loading on the performance of NTFs is not well understood. A laboratory-scale NTF system was operated in recirculation mode, with the objective of removing ammonia and CoC simultaneously. The efficiency of a high rate NTF for removal both of low concentration of ammonia (5 mg NH4-N L(-1)) and different concentrations of CoC in the presence of an exogenous organic carbon substrate (30 mg total organic carbon (TOC) L(-1)) was investigated. In the presence of exogenous organic carbon, the results demonstrated that the high rate NTF was able to successfully remove most of the CoCs investigated, with the removal ranging from 20.2% to 87.54%. High removal efficiencies were observed for acetaminophen (87.54%), bisphenol A (86.60%), trimethoprim (86.24%) and 17α-ethynylestradiol (80.60%). It was followed by the medium removal efficiency for N, N-diethyl-m-toluamide (61.31%) and atrazine (56.90%). In contrast, the removal of caffeine (28.43%) and benzotriazole (20.20%) was poorer in the presence of exogenous organic carbon. The removal efficiency for CoC was also compared with the results obtained in our previous study in the absence of exogenous organic carbon. The results showed that the addition of exogenous organic carbon was able to improve the removal of some of the CoC. Significant TOC percentage removals (45.68%-84.43%) and ammonia removal rate (mean value of 0.44 mg NH4-N L(-1) h(-1)) were also achieved in this study. The findings from this study provide valuable information for optimising the efficiency of high rate NTF for the removal of ammonia, CoC and TOC. Copyright © 2016 Elsevier Ltd. All rights reserved.

MINERAL NITROGEN SOURCES (N-NO3- AND N-NH4+ ON GROWTH OF GRÁPIA (Apuleia leiocarpa (Vog. Macbride SEEDLINGS

Directory of Open Access Journals (Sweden)

Fernando Teixeira Nicoloso

2010-08-01

Full Text Available Grápia (Apuleia leiocarpa (Vog. Macbride is an important native forest species that has been in extinction process. The aim of this study was to evaluate the effect of mineral nitrogen source on growth of grápia seedlings. Five variations in the concentration of N-NO3- and N-NH4+ (5:0, 4:1, 2,5:2,5, 1:4, and 0:5 mM of N were tested in an entirely random statistical design with 16 replicates. The experimental unity consisted of a vessel containing 3,0 kg of a Paleudalf soil and two plants, under glasshouse conditions. From 60 to 150 days after fertilization (DAF, the plant growth and soil pH were monthly analyzed from four replicates randomly taken. Independently of the nitrogen source used, the soil pH decreased, and on 150 DAF the smallest pH variation was 0.33 and the largest one was 0.47 pH units, respectively, on treatments with 5 N-NO3-:0 N-NH4+ and 0 N-NO3-:5 N-NH4+ ratios. The presence of N-NH4+, from 1 to 5 mM, induced necrosis in old leaves and their ulterior abscission. To 150 DAF, in the presence of 5 mM N-NH4+, the plant survival was reduced to 31%. The effect of nitrogen sources on plant growth appeared to be depended on plant age and/or of their transformations in the soil. To 120 DAF, the presence of N-NH4+ from 2,5 to 5 mM reduced the number of stalk nodes, plant height, stem diameter, dry weight of leaves, of stem, of roots, and of the whole plant. However, to 150 DAF, because of the regain on the growth rate, these differences were not observed, with exception of the root/shoot dry weight ratio that was reduced on the exclusive presence of N-NH4+. The suitable N-NO3-:N-NH4+ ratio in the fertilization to grow grápia seedlings, can not exceed, respectively, 4:1.

Biological removal of nitrate and ammonium under aerobic atmosphere by Paracoccus versutus LYM.

Science.gov (United States)

Shi, Zhuang; Zhang, Yu; Zhou, Jiti; Chen, Mingxiang; Wang, Xiaojun

2013-11-01

The bacterium isolated from sea sludge Paracoccus versutus LYM was characterized with the ability of aerobic denitrification. Strain LYM performs perfect activity in aerobically converting over 95% NO3(-)-N (approximate 400mg L(-1)) to gaseous products via nitrite with maximum reduction rate 33 mg NO3(-)-N L(-1) h(-1). Besides characteristic of aerobic denitrification, strain LYM was confirmed in terms of the ability to be heterotrophic nitrification and aerobic denitrification (HNAD) with few accumulations of intermediates. After the nitrogen balance and enzyme assays, the putative nitrogen pathway of HNAD could be NH4(+) → NH2OH → NO2(-)→ NO3(-), then NO3(-) was denitrified to gaseous products via nitrite. N2 was sole denitrification product without any detection of N2O by gas chromatography. Strain LYM could also simultaneously remove ammonium and additional nitrate. Meanwhile, the accumulated nitrite had inhibitory effect on ammonium reduction rate. Copyright © 2013 Elsevier Ltd. All rights reserved.

One-pot synthesis of ternary zero-valent iron/phosphotungstic acid/g-C3N4 composite and its high performance for removal of arsenic(V) from water

Science.gov (United States)

Chen, Chunhua; Xu, Jia; Yang, Zhihua; Zhang, Li; Cao, Chunhua; Xu, Zhihua; Liu, Jiyan

2017-12-01

Ternary zero-valent iron/phos photungstic acid/g-C3N4 composite (Fe0@PTA/g-C3N4) was synthesized via photoreduction of iron (II) ions assisted by phosphotungstic acid (PTA) over g-C3N4 flakes. The as-prepared Fe0@PTA/g-C3N4 was investigated for removal of As(III) and As(V) species from water. The result showed that Fe0@PTA/g-C3N4 exhibited a better performance for As(V) removal than As(III) species from water, and the maximum adsorption capacity for As(V) was 70.3 mg/g, much higher than most of the reported adsorbents. As(V) removal by the Fe0@PTA/g-C3N4 adsorbent is mainly via a chemical process, synergistically occurring of reduction of As(V) and oxidation of Fe0. Moreover, the Fe0@PTA/g-C3N4 adsorbent showed effective As(V) removal from the simulated industrial wastewater and underground water. This study demonstrates that Fe0@PTA/g-C3N4 can be a potential adsorbent for As(V) removal due to its high performance, and simple one-pot synthesis process.

Removal of NO from flue gas by aqueous chlorine-dioxide scrubbing solution in a lab-scale bubbling reactor.

Science.gov (United States)

Deshwal, Bal Raj; Jin, Dong Seop; Lee, Si Hyun; Moon, Seung Hyun; Jung, Jong Hyeon; Lee, Hyung Keun

2008-02-11

The present study attempts to clean up nitric oxide from the simulated flue gas using aqueous chlorine-dioxide solution in the bubbling reactor. Chlorine-dioxide is generated by chloride-chlorate process. Experiments are carried out to examine the effect of various operating variables like input NO concentration, presence of SO(2), pH of the solution and NaCl feeding rate on the NO(x) removal efficiency at 45 degrees C. Complete oxidation of nitric oxide into nitrogen dioxide occurred on passing sufficient ClO(2) gas into the scrubbing solution. NO is finally converted into nitrate and ClO(2) is reduced into chloride ions. A plausible reaction mechanism concerning NO(x) removal by ClO(2) is suggested. DeNO(x) efficiency increased slightly with the increasing input NO concentration. The presence of SO(2) improved the NO(2) absorption but pH of solution showed marginal effect on NO(2) absorption. NO(x) removal mechanism changed when medium of solution changed from acidic to alkaline. A constant NO(x) removal efficiency of about 60% has been achieved in the wide pH range of 3-11 under optimized conditions.

Facile one-pot construction of α-Fe_2O_3/g-C_3N_4 heterojunction for arsenic removal by synchronous visible light catalysis oxidation and adsorption

International Nuclear Information System (INIS)

Sun, Suwen; Ji, Chunnuan; Wu, Lingling; Chi, Shenghua; Qu, Rongjun; Li, Yan; Lu, Yangxiao; Sun, Changmei; Xue, Zhongxin

2017-01-01

α-Fe_2O_3/g-C_3N_4 composites with heterojunction were prepared by facile one-pot synthesis using ferric chloride and dicyandiamide as precursors. The newly formed composites were applied to remove arsenic from aqueous solution for the first time through synchronous visible light catalysis oxidation and adsorption. α-Fe_2O_3/g-C_3N_4 composites were characterized by wide-angle X-ray powder diffraction, transmission electron microscopy, high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, UV–Vis diffuse reflectance spectroscopy, and BET surface analysis. Under visible light irradiation, As(III) was oxidized to As(V) efficiently on the surface of α-Fe_2O_3/g-C_3N_4. In addition, the oxidized arsenic could be adsorbed in situ, resulting in the effective arsenic removal. The enhancement of photocatalytic activity the composites was attributed to the construction of heterojunction between α-Fe_2O_3 and g-C_3N_4. A possible oxidation mechanism of the as-composites for As(III) under visible light irradiation was also elucidated. - Highlights: • α-Fe_2O_3/g-C_3N_4 composites with heterojunction was prepared by facile one-pot synthesis. • The photocatalytic activity of α-Fe_2O_3/g-C_3N_4 composites under visible light irradiation for As(III) was evaluated. • Synchronous visible light catalysis oxidation and adsorption were achieved for the removal of arsenic. • The reasonable oxidation mechanism of the composites for As(III) under visible light irradiation was investigated.

Compressible and Recyclable Monolithic g-C3N4/Melamine Sponge: A Facile Ultrasonic-coating Approach and Enhanced Visible-light Photocatalytic Activity

Science.gov (United States)

Yang, Ye; Zhang, Qian; Zhang, Ruiyang; Ran, Tao; Wan, Wenchao; Zhou, Ying

2018-05-01

Powdery photocatalysts seriously restrict their practical application due to the difficult recycle and low photocatalytic activity. In this work, a monolithic g-C3N4/melamine sponge (g-C3N4/MS) was successfully fabricated by a cost-effective ultrasonic-coating route, which is easy to achieve the uniform dispersion and firm loading of g-C3N4 on MS skeleton. The monolithic g-C3N4/MS entirely inherits the porous structure of MS and results in a larger specific surface area (SSA) than its powdery counterpart. Benefit from this monolithic structure, g-C3N4/MS gains more exposed active sites, enhanced visible-light absorption and separation of photogenerated carriers, thus achieving noticeable photocatalytic activity on nitric oxide (NO) removal, rhodamine B (RhB) degradation and CO2 reduction. Specifically, NO removal ratio is as high as 78.6% which is 4.5 times higher than that of the powdery g-C3N4, while RhB degradation rate reaches 97.88%, and yield rate of CO and CH4 attains 7.48 and 3.93 μmol g-1 h-1. Importantly, the features of low-density, high porosity, good elasticity and firmness, not only endow g-C3N4/MS with flexibility in various environmental applications, but also make it easy to recycle and stable for long-time application. Our work provides a feasible approach to fabricate novel monolithic photocatalysts with large-scale production and application.

Observation of advanced particle removal rates in pump limiter simulation experiments

International Nuclear Information System (INIS)

Goebel, D.M.; Conn, R.W.

1984-05-01

The performance of particle removal schemes for density and impurity control in tokamaks and mirror machines depends strongly on the plasma parameters and local recycling near the plasma neutralizier plates and gas pumping ducts. The relationship between plasma density, electron temperature, ion energy and gas flow and particle removal rate through a pumping duct located near a plasma neutralizer plate has been experimentally investigated in the steady state plasma device PISCES. Results indicate that initially the particle removal by pumps at the end of the duct is proportional to the plasma flux to the plate. A nonlinear increase in the pumping rate occurs when the ionization mean free path for neutrals from the plate becomes less than the plasma radius. The transition from a transparent to an opaque plasma due to local ionization of the neutrals produced at the neutralizer plate greatly enhances the particle removal rate by recycling of the neutral gas as it flows away from the neutralizer plate or out of the pumping ducts. Parameters were varied to determine the importance of ballistic scattering of higher energy ions from the plate, but no effects were found in these experiments

Monoclinic α-Bi2O3 photocatalyst for efficient removal of gaseous NO and HCHO under visible light irradiation

International Nuclear Information System (INIS)

Ai Zhihui; Huang Yu; Lee Shuncheng; Zhang Lizhi

2011-01-01

Research highlights: → We got the monoclinic α-Bi 2 O 3 powders after the calcinations of the plate-like (BiO) 2 CO 3 precursors at 500 deg. C for 4 h. → The synthetic α-Bi 2 O 3 showed high visible light photocatalytic activity for removal of NO and HCHO. - Abstract: The investigation was focused on the visible-light-driven photocatalytic removal of gaseous NO and HCHO at typical indoor air concentration over synthetic α-Bi 2 O 3 . Monoclinic α-Bi 2 O 3 was synthesized via calcination of hydrothermally prepared (BiO) 2 CO 3 precursor at 500 deg. C for 4 h. The synthetic α-Bi 2 O 3 samples were systematically characterized by XRD, SEM, FT-IR, and UV-vis diffuse reflectance spectra (DRS). The optical band gap energy of the resulting α-Bi 2 O 3 was estimated to be 2.72 eV from the UV-vis absorption spectra. Comparing with the commercial Bi 2 O 3 counterpart, the fabricated α-Bi 2 O 3 showed superior visible-light-induced photocatalytic activity on degradation of nitrogen monoxide (NO) and formaldehyde (HCHO) at typical indoor air concentration. No obvious deactivation of synthetic α-Bi 2 O 3 was observed during the prolonged photocatalytic reaction. This work suggests that the synthesized monoclinic α-Bi 2 O 3 with suitable band gap and high activity is promising photocatalyst for indoor air purification.

[NH4+-N removal stability of zeolite media packed multistage-biofilm system for coke-plant wastewater treatment].

Science.gov (United States)

Zhao, Wen-Tao; Huang, Xia; He, Miao; Zhang, Peng-Yi; Zuo, Chen-Yan

2009-02-15

The practical ammonia stripping effectiveness of coke-plant wastewater treatment may vary widely, and high NH4+-N shock loading will lead to the fluctuation of residual NH4+-N concentration of biological effluent. A zeolite media packed multistage-biofilm system (ZMBS) was used for coke-plant wastewater treatment for enhancing the NH4+-N treatment ability of the bio-system to shock loading, as well as achieving high COD removal efficiency. Treatment performance during steady-state and shock loading and transformation of organic pollutants in the system were investigated systematically. The experiment results indicated that when the system was operated at NH4+-N loading 0.21 kg/(m3 x d) and COD loading NH4+-N and COD concentrations were (2.2 +/- 1.2) mg/L, (228 +/- 60) mg/L with average removal efficiencies of (99.1 +/- 0.5)% and (86.0 +/- 2.6)%. During the twice NH4+-N shock loadings [0.03 kg/(m3 x d) and 0.06 kg/(m3 x d)], ZMBS showed a strong resisting ability with average removal efficiencies of 99.0% and 92.9% higher than those of a compared system's 96.8% and 89.3%. By monitoring the change of water quality along the length of the ZMBS's cells, two function zones for different pollutant removal were found to exist, named as decarbonization/nitrification (C/N) zone and nitrification (N) zone, and the NH4+-N removal rate in N zone was 2-8 times as that in C/N zone. TOC concentrations of organic matters with relative molecular weight 1 x 10(4), were 227.6, 104.8 and 35.0 mg/L in raw wastewater, and 31.2, 22.9 and 31.5 mg/L in the effluent, respectively. Organic matters with relative molecular weight 1x 10(3) were the main remained substances in the effluent.

Comparison of different ecological remediation methods for removing nitrate and ammonium in Qinshui River, Gonghu Bay, Taihu Lake.

Science.gov (United States)

Wang, Hao; Li, Zhengkui; Han, Huayang

2017-01-01

Ecological remediation is one of the most practical methods for removing nutrients from river ecosystems. In this study, transformation and fate of nitrate and ammonium among four different ecological restoration treatments were investigated by stable 15 N isotope pairing technique combined with quantitative polymerase chain reaction and high-throughput sequencing technology. The results of 15 N mass-balance model showed that there were three ways to the fate of nitrogen: precipitated in the sediment, absorbed by Elodea nuttallii (E. nuttallii), and consumed by microbial processes (denitrification and anaerobic ammonium oxidation (anammox)). The results shown that the storage of 15 NH 4 + in sediments was about 1.5 times as much as that of 15 NO 3 - . And much more 15 NH 4 + was assimilated by E. nuttallii, about 2 times as much as 15 NO 3 - . Contrarily, the rate of microbial consuming 15 NO 3 - was higher than converting 15 NH 4 + . As for the group with 15 NO 3 - added, 29.61, 45.26, 30.66, and 51.95 % were accounted for 15 N-labeled gas emission. The proportions of 15 NH 4 + loss as 15 N-labeled gas were 16.06, 28.86, 16.93, and 33.09 % in four different treatments, respectively. Denitrification and anammox were the bacterial primary processes in N 2 and N 2 O production. The abundances of denitrifying and anammox functional genes were relatively higher in the treatment with E. nuttallii-immobilized nitrogen cycling bacteria (E-INCB) assemblage technology applied. Besides, microbial diversity increased in the treatment with E. nuttallii and INCB added. The 15 NO 3 - removal rates were 35.27, 49.42, 50.02, and 65.46 % in four different treatments. And the removal rates of 15 NH 4 + were 24, 34.38, 48.84, and 57.74 % in treatments A, B, C, and D, respectively. The results indicated that E-INCB assemblage technology could significantly promote the nitrogen cycling and improve nitrogen removal efficiency.

Synthesis, characterization and photocatalytic activity of WO3/TiO2 for NO removal under UV and visible light irradiation

International Nuclear Information System (INIS)

Luévano-Hipólito, E.; Martínez-de la Cruz, A.; López-Cuellar, E.; Yu, Q.L.; Brouwers, H.J.H.

2014-01-01

Samples with different proportions WO 3 /TiO 2 were prepared by co-precipitation method followed by a heat treatment. The samples were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance spectroscopy (DRS), and adsorption–desorption N 2 isotherms (BET). The photocatalytic properties of WO 3 /TiO 2 samples were evaluated in the photo-oxidation reaction of nitric oxide (NO) under UV and visible light irradiation. The highest photocatalytic activity was observed in the WO 3 /TiO 2 sample with a composition of 80% mole of TiO 2 . Among the different substrates used for supporting the photocatalyst, the best results were reached over concrete and glass when it was exposed to UV and visible light irradiation, respectively. In overall, the photocatalytic efficiency of the synthesized materials was higher under UV than visible light irradiation. - Highlights: • WO 3 /TiO 2 prepared in simple way show high photocatalytic activity for NO removal. • The concrete was the best substrate to the performance of WO 3 /TiO 2 with UV radiation. • The glass was the best substrate to the performance of WO 3 /TiO 2 with visible radiation

Wintertime Overnight NOx Removal in a Southeastern United States Coal-fired Power Plant Plume: A Model for Understanding Winter NOx Processing and its Implications

Science.gov (United States)

Fibiger, Dorothy L.; McDuffie, Erin E.; Dubé, William P.; Aikin, Kenneth C.; Lopez-Hilfiker, Felipe D.; Lee, Ben H.; Green, Jaime R.; Fiddler, Marc N.; Holloway, John S.; Ebben, Carlena; Sparks, Tamara L.; Wooldridge, Paul; Weinheimer, Andrew J.; Montzka, Denise D.; Apel, Eric C.; Hornbrook, Rebecca S.; Hills, Alan J.; Blake, Nicola J.; DiGangi, Josh P.; Wolfe, Glenn M.; Bililign, Solomon; Cohen, Ronald C.; Thornton, Joel A.; Brown, Steven S.

2018-01-01

Nitric oxide (NO) is emitted in large quantities from coal-burning power plants. During the day, the plumes from these sources are efficiently mixed into the boundary layer, while at night, they may remain concentrated due to limited vertical mixing during which they undergo horizontal fanning. At night, the degree to which NO is converted to HNO3 and therefore unable to participate in next-day ozone (O3) formation depends on the mixing rate of the plume, the composition of power plant emissions, and the composition of the background atmosphere. In this study, we use observed plume intercepts from the Wintertime INvestigation of Transport, Emissions and Reactivity campaign to test sensitivity of overnight NOx removal to the N2O5 loss rate constant, plume mixing rate, background O3, and background levels of volatile organic compounds using a 2-D box model of power plant plume transport and chemistry. The factor that exerted the greatest control over NOx removal was the loss rate constant of N2O5. At the lowest observed N2O5 loss rate constant, no other combination of conditions converts more than 10% of the initial NOx to HNO3. The other factors did not influence NOx removal to the same degree.

Wintertime Overnight NOx Removal in a Southeastern United States Coal-Fired Power Plant Plume: A Model for Understanding Winter NOx Processing and Its Implications

Science.gov (United States)

Fibiger, Dorothy L.; McDuffie, Erin E.; Dube, William P.; Aikin, Kenneth C.; Lopez-Hilifiker, Felipe D.; Lee, Ben H.; Green, Jaime R.; Fiddler, Marc N.; Holloway, John S.; Ebben, Carlena;

Rate and extent of aqueous perchlorate removal by iron surfaces.

Science.gov (United States)

Moore, Angela M; De Leon, Corinne H; Young, Thomas M

2003-07-15

The rate and extent of perchlorate reduction on several types of iron metal was studied in batch and column reactors. Mass balances performed on the batch experiments indicate that perchlorate is initially sorbed to the iron surface, followed by a reduction to chloride. Perchlorate removal was proportional to the iron dosage in the batch reactors, with up to 66% removal in 336 h in the highest dosage system (1.25 g mL(-1)). Surface-normalized reaction rates among three commercial sources of iron filings were similar for acid-washed samples. The most significant perchlorate removal occurred in solutions with slightly acidic or near-neutral initial pH values. Surface mediation of the reaction is supported by the absence of reduction in batch experiments with soluble Fe2+ and also by the similarity in specific reaction rate constants (kSA) determined for three different iron types. Elevated soluble chloride concentrations significantly inhibited perchlorate reduction, and lower removal rates were observed for iron samples with higher amounts of background chloride contamination. Perchlorate reduction was not observed on electrolytic sources of iron or on a mixed-phase oxide (Fe3O4), suggesting that the reactive iron phase is neither pure zerovalent iron nor the mixed oxide alone. A mixed valence iron hydr(oxide) coating or a sorbed Fe2+ surface complex represent the most likely sites for the reaction. The observed reaction rates are too slow for immediate use in remediation system design, but the findings may provide a basis for future development of cost-effective abiotic perchlorate removal techniques.

Efeito da taxa de carregamento sobre a remoção de poluentes de esgoto em sistemas alagados construídos Effect of loading rate on removal of pollutants from wastewater in constructed wetlands

Directory of Open Access Journals (Sweden)

Antonio T. de Matos

2013-04-01

Full Text Available Objetivou-se estudar o efeito da taxa de carregamento sobre a eficiência de sistemas alagados, construídos de escoamento horizontal subsuperficial (SAC-EHSS, em remover poluentes de esgoto sanitário. Os SAC-EHSS foram alimentados com efluente proveniente de tanque séptico, sob taxas de carregamento orgânico volumétrico (TCO V de 53 a 231 g m-3d-1 de demanda química de oxigênio (DQO total e as associadas taxas de carregamento (TC V de demanda química de oxigênio solúvel, sólidos suspensos totais (SST, nitrogênio total (N-Total e fósforo total (P-Total. Para avaliação de desempenho dos SAC-EHSS, as mesmas variáveis foram quantificadas em seu efluente. Relação linear e positiva foi obtida entre as taxas de remoção de DQO total, DQO solúvel e SST, e as TC V, nas faixas em que foram aplicadas, além de não terem sido observados efeitos negativos desta variável sobre a eficiência na remoção desses poluentes. As taxas de remoção de N-Total e P-Total não apresentaram, entretanto, tendência de aumento com a TC V aplicada nos SAC- EHSS, cultivados com taboa e utilizados no tratamento de efluente sanitário. As cargas aplicadas desses nutrientes devem ser consideradas referenciais no dimensionamento desses sistemas, caso se queira maximizar a remoção global de poluentes da água residuária.This research aimed to study the effect of loading rate on the efficiency of constructed wetlands with horizontal subsurface flow (CW-HSSF to remove pollutants from wastewater. The CW-HSSF were fed with effluent from septic tank under volumetric organic loading rate (OLR V of 53 to 231 g m-3d-1 of chemical oxygen demand (total-COD and associated loading rates (LR V of soluble chemical oxygen demand (soluble COD, total suspended solids (TSS, total nitrogen (total-N and total phosphorus (total-P. To evaluate the performance of CW-HSSF the same variables were quantified in its effluent. Linear and positive relationship was found between the

Wheat straw biochar-supported nanoscale zerovalent iron for removal of trichloroethylene from groundwater.

Directory of Open Access Journals (Sweden)

Hui Li

Full Text Available This study synthesized the wheat straw biochar-supported nanoscale zerovalent iron (BC-nZVI via in-situ reduction with NaBH4 and biochar pyrolyzed at 600°C. Wheat straw biochar, as a carrier, significantly enhanced the removal of trichloroethylene (TCE by nZVI. The pseudo-first-order rate constant of TCE removal by BC-nZVI (1.079 h-1 within 260 min was 1.4 times higher and 539.5 times higher than that of biochar and nZVI, respectively. TCE was 79% dechlorinated by BC-nZVI within 15 h, but only 11% dechlorinated by unsupported nZVI, and no TCE dechlorination occurred with unmodified biochar. Weakly acidic solution (pH 5.7-6.8 significantly enhanced the dechlorination of TCE. Chloride enhanced the removal of TCE, while SO42-, HCO3- and NO3- all inhibited it. Humic acid (HA inhibited BC-nZVI reactivity, but the inhibition decreased slightly as the concentration of HA increased from 40 mg∙L-1 to 80 mg∙L-1, which was due to the electron shutting by HA aggregates. Results suggest that BC-nZVI was promising for remediation of TCE contaminated groundwater.

Sequential Aeration of Membrane-Aerated Biofilm Reactors for High-Rate Autotrophic Nitrogen Removal: Experimental Demonstration

DEFF Research Database (Denmark)

Pellicer i Nàcher, Carles; Sun, Sheng-Peng; Lackner, Susanne

2010-01-01

One-stage autotrophic nitrogen (N) removal, requiring the simultaneous activity of aerobic and anaerobic ammonium oxidizing bacteria (AOB and AnAOB), can be obtained in spatially redox-stratified biofilms. However, previous experience with Membrane-Aerated Biofilm Reactors (MABRs) has revealed...... a difficulty in reducing the abundance and activity of nitrite oxidizing bacteria (NOB), which drastically lowers process efficiency. Here we show how sequential aeration is an effective strategy to attain autotrophic N removal in MABRs: Two separate MABRs, which displayed limited or no N removal under...... continuous aeration, could remove more than 5.5 g N/m2/day (at loads up to 8 g N/m2/day) by controlled variation of sequential aeration regimes. Daily averaged ratios of the surficial loads of O2 (oxygen) to NH4+ (ammonium) (LO2/LNH4) were close to 1.73 at this optimum. Real-time quantitative PCR based on 16...

Development of an airborne three-channel LED-based broadband cavity enhanced absorption spectrometer: towards an improved understanding of nighttime chemistry of NO3 and N2O5 in northwest Europe

Science.gov (United States)

Ouyang, Bin

2015-04-01

A three-channel cavity-enhanced absorption spectrometer capable of covering a broad UV-vis spectrum range has been developed in Cambridge for deployment on board the UK FAAM BAe-146 atmospheric research aircraft for measuring in situ concentrations of important atmospheric absorbers such as NO3, N2O5, NO2, IO and H2O and also aerosol extinction. So far this instrument has been deployed in two aircraft campaigns (the ROle of Nighttime chemistry in controlling the Oxidative Capacity of the atmOsphere, RONOCO, during July 2010 and January 2011; and the Coordinated Airborne Studies in the Tropics, CAST, during February 2014) with focuses on measuring NO2/NO3/N2O5 (for RONOCO) and IO (for CAST). In this talk, I will start by briefly presenting the working principle, design consideration, sensitivity test as well as intercomparison results of this novel aircraft instrument. I will then move on to present recent results from the analysis of the RONOCO campaign data, to illustrate the spatial and temporal variability of nighttime chemistry processes revealed by the high-resolution NO3 and N2O5 data collected. Significant improvements were made towards a better understanding of the oxidation of reactive VOCs by NO3 and O3 and the contribution of peroxy radicals (HO2 and RO2, of which only HO2 was successfully measured) to NO3 direct losses, and towards determining factors (organics and nitrate components of the aerosol particles, and relative humidity) that greatly influence the rate of N2O5 uptake by aerosol particles as well as directly probing the role of cloud, rain and ice scavenging in removing N2O5, in this typical northwest European environment.

Moisture removal rate for air dehumidification by triethylene glycol in a structured packed column

International Nuclear Information System (INIS)

Elsarrag, Esam

2007-01-01

In this investigation, a desiccant dehumidifier is tested for different ranges of liquid to air flow rate ratios to expand the validity range of the results. Theoretical and experimental studies of the simultaneous heat and mass transfer to evaluate the moisture removal rate are conducted. The model predictions are compared with experimental results with very good agreement. Through the experimental study, the important design variables that affect the moisture removal rate are defined and compared with previous studies. The correlation found in the literature is assessed, and the errors are reported. The parameters that are varied during the experiments included the air and liquid flow rates, the air humidity ratio, the desiccant equilibrium humidity and the packing height. It is found that the liquid flow rate has no significant effect on the moisture removal rate when the liquid to air flow ratio has exceeded the value of 2

Modeling the CO2 and N2O Emissions From Stover Removal for Biofuel Production From Continuous Corn Production in Iowa

Science.gov (United States)

Paustian, K.; Killian, K.; Brenner, J.

2003-12-01

Corn stover, an agricultural residue, can be used as feedstock for near term bioethanol production and is available today at levels that can significantly impact energy supply. We evaluated the environmental impact of such a large-scale change in agricultural practices on green house gas production, soil erosion and soil carbon using the Century model. Estimates of soil C changes and GHG emissions were performed for the 99 counties in Iowa where previous environmental, management and erosion data was available. We employed climate, soil and historical management databases from a separate USDA-funded project as input to Century. RUSLE estimates of the residue requirements for acceptable soil loss rates under continuous corn agriculture were available from a previous study done Dr. Richard Nelson (Enersol Resources). Two mulch tillage and a no-till systems, where erosion estimates were available, were used as the basis for the simulations. Century simulations of these systems were run under a variety of stover removal rates. For each soil type within each county the model was run for 15 years (1980-1995) under continuous corn with convention tillage, and full residue return. Model simulation of crop yields and residue production were then calibrated to match those used by the Polysys model team at Oak Ridge and the simulation was repeated with the addition of the three corn tillage regimes, and several residue removal rates. County-average soil C changes (and net CO2 emissions) were calculated as area-weighted averages of the individual soil types in each county. For this study, we have utilized the IPCC approach to estimate annual N2O emissions. At low or zero residue removal rates, county-averaged soil C stocks were predicted to increase (i.e. net CO2 emissions are negative). Where the allowable residue removal rates (based on erosion tolerance) for mulch-tillage are on the order of 40-50% or more, the reduced input of C is such that the soils no longer sequester C

Factorial study of rain garden design for nitrogen removal

Science.gov (United States)

Abstract Nitrate (〖NO〗_3^--N ) removal studies in bioretention systems showed great variability in removal rates and in some cases 〖NO〗_3^--N was exported. A 3-way factorial design (2 x 2 x 4) was devised for eight outdoor un-vegetated rain gardens to evaluate the effects of ...

Comparison of NH4+-N and NO3--N nutrition in hybrid and conventional rice at the late growth stage

International Nuclear Information System (INIS)

Yang Xiaoe; Sun Xi

1990-01-01

The difference of NH 4 + -N/NO 3 - -N nutrition between hybrid and conventional rice varieties at the late growth stage was studied by using 15 N-tracer technique. The results showed that the nitrate fertilizer utilization efficiency by the hybrid rice after anthesis was 7.8% higher than that by the ordinary rice variety, and the nitrate fertilizer recovery fraction by the former was 13.2% greater than that by the latter. The varietal difference in NO 3 - -N uptake and utilization was almost twice as that in NH 4 + -N. It was also showed that 15 N distribution in ear of the hybrid rice was about 20% greater than that of the conventional variety, but there were no obvious differences between NO 3 - -N and NH 4 + -N. However, 15 N distribution in the lower node leaves and root was found to be significant higher with NO 3 - -N than that with NH 4 + -N in both rice varieties, particularly in the hybrid rice. Compared with NH 4 + -N, NO 3 - -N top-dressing before anthesis was observed to have much greater positive effects on the uptake of calcium and magnesium and the growth of the superficial root and the grain yield of the tested rice varieties, especially of the hybrid rice

Development of an attached growth reactor for NH₄-N removal at a drinking water supply system in Kathmandu Valley, Nepal.

Science.gov (United States)

Khanitchaidecha, Wilawan; Shakya, Maneesha; Nakano, Yuichi; Tanaka, Yasuhiro; Kazama, Futaba

2012-01-01

Higher concentrations of ammonium (NH(4)-N) and iron (Fe) than a standard for drinking are typical characteristics of groundwater in the study area. To remove NH(4)-N and Fe, the drinking water supply system in this study consists of a series of treatment units (i.e., aeration and sedimentation, filtration, and chlorination); however, NH(4)-N in treated water is higher than a standard for drinking (i.e., removal efficiency. In accordance with raw groundwater characteristics in the area, effects of low inorganic carbon (IC) and phosphate (PO(4)-P) and high Fe on the removal efficiency were also investigated. The results showed a significant increase in NH(4)-N removal efficiency with reactor length and carrier area. A low IC and PO(4)-P had no effect on NH(4)-N removal, whereas a high Fe decreased the efficiency significantly. The first 550 days operation of a pilot-scale reactor installed in the drinking water supply system showed a gradual increase in the efficiency, reaching to 95-100%, and stability in the performance even with increased flow rate from 210 to 860 L/day. The high efficiency of the present work was indicated because only less than 1 mg of NH(4)-N/L was left over in the treated water.

Integrated removal of organic load, P, N, on a filters serial system, anaerobic, anoxic and aerobic on dynamic conditions

International Nuclear Information System (INIS)

Correa Mauricio Andres; Sierra, Jorge Humberto

2004-01-01

This paper shows the results obtained during the operation under dynamic conditions of a three biofilters serial system, anaerobic, anoxic and aerobic at lab scale to evaluate the N, P, and organic matter removal. The reactors were continuously fed for 200 days, including the adherence and stability periods, with hydraulic retention time among 2,27 and 0,66 d. for the ANABF and among 1,5 and 0,5 d. for the ANXBF. The adherence period was followed by a control of SSV and the DQO removal in each BF. After good results of adherence the system was fed with an initial average volumetric organic load of 0,441 kg DQO/m 3 /d. and gradually increase during the results of DQO removal over the 50%, until the achievement of the system stability for a maximum organic load of 1,5 kg. The reactor control was made by DQO, PO 4 3 , NTK, NO 2 , NO 3 , SS and alkalinity, determined at enter and exit of each reactor. The removal results for the system of growing adherence was among 90-96% for DQO, 80-90% for total P, and 65-70% for total N

Digestate application in landfill bioreactors to remove nitrogen of old landfill leachate.

Science.gov (United States)

Peng, Wei; Pivato, Alberto; Lavagnolo, Maria Cristina; Raga, Roberto

2018-04-01

Anaerobic digestion of organics is one of the most used solution to gain renewable energy from waste and the final product, the digestate, still rich in putrescible components and nutrients, is mainly considered for reutilization (in land use) as a bio-fertilizer or a compost after its treatment. Alternative approaches are recommended in situations where conventional digestate management practices are not suitable. Aim of this study was to develop an alternative option to use digestate to enhance nitrified leachate treatment through a digestate layer in a landfill bioreactor. Two identical landfill columns (Ra and Rb) filled with the same solid digestate were set and nitrified leachate was used as influent. Ra ceased after 75 day's operation to get solid samples and calculate the C/N mass balance while Rb was operated for 132 days. Every two or three days, effluent from the columns were discarded and the columns were refilled with nitrified leachate (average N-NO 3 - concentration = 1,438 mg-N/L). N-NO 3 - removal efficiency of 94.7% and N-NO 3 - removal capacity of 19.2 mg N-NO 3 - /gTS-digestate were achieved after 75 days operation in Ra. Prolonging the operation to 132 days in Rb, N-NO 3 - removal efficiency and N-NO 3 - removal capacity were 72.5% and 33.1 mg N-NO 3 - /gTS-digestate, respectively. The experimental analysis of the process suggested that 85.4% of nitrate removal could be attributed to denitrification while the contribution percentage of adsorption was 14.6%. These results suggest that those solid digestates not for agricultural or land use, could be used in landfill bioreactors to remove the nitrogen from old landfill leachate. Copyright © 2018 Elsevier Ltd. All rights reserved.

Coupled nutrient removal and biomass production with mixed algal culture: impact of biotic and abiotic factors.

Science.gov (United States)

Su, Yanyan; Mennerich, Artur; Urban, Brigitte

2012-08-01

The influence of biotic (algal inoculum concentration) and abiotic factors (illumination cycle, mixing velocity and nutrient strength) on the treatment efficiency, biomass generation and settleability were investigated with selected mixed algal culture. Dark condition led to poor nutrient removal efficiency. No significant difference in the N, P removal and biomass settleability between continuous and alternating illumination was observed, but a higher biomass generation capability for the continuous illumination was obtained. Different mixing velocity led to similar phosphorus removal efficiencies (above 98%) with different retention times. The reactor with 300 rpm mixing velocity had the best N removal capability. For the low strength wastewater, the N rates were 5.4±0.2, 9.1±0.3 and 10.8±0.3 mg/l/d and P removal rates were 0.57±0.03, 0.56±0.03 and 0.72±0.05 mg/l/d for reactors with the algal inoculum concentration of 0.2, 0.5 and 0.8 g/l, respectively. Low nutrient removal efficiency and poor biomass settleability were obtained for high strength wastewater. Copyright © 2012 Elsevier Ltd. All rights reserved.

Effect of COD/N ratio on N2O production during nitrogen removal by aerobic granular sludge.

Science.gov (United States)

Velho, V F; Magnus, B S; Daudt, G C; Xavier, J A; Guimarães, L B; Costa, R H R

2017-12-01

N 2 O-production was investigated during nitrogen removal using aerobic granular sludge (AGS) technology. A pilot sequencing batch reactor (SBR) with AGS achieved an effluent in accordance with national discharge limits, although presented a nitrite accumulation rate of 95.79% with no simultaneous nitrification-denitrification. N 2 O production was 2.06 mg L -1 during the anoxic phase, with N 2 O emission during air pulses and the aeration phase of 1.6% of the nitrogen loading rate. Batch tests with AGS from the pilot reactor verified that at the greatest COD/N ratio (1.55), the N 2 O production (1.08 mgN 2 O-N L -1 ) and consumption (up to 0.05 mgN 2 O-N L -1 ), resulted in the lowest remaining dissolved N 2 O (0.03 mgN 2 O-N L -1 ), stripping the minimum N 2 O gas (0.018 mgN 2 O-N L -1 ). Conversely, the carbon supply shortage, under low C/N ratios, increased N 2 O emission (0.040 mgN 2 O-N L -1 ), due to incomplete denitrification. High abundance of ammonia-oxidizing and low abundance of nitrite-oxidizing bacteria were found, corroborating the fact of partial nitrification. A denitrifying heterotrophic community, represented mainly by Pseudoxanthomonas, was predominant in the AGS. Overall, the AGS showed stable partial nitrification ability representing capital and operating cost savings. The SBR operation flexibility could be advantageous for controlling N 2 O emissions, and extending the anoxic phase would benefit complete denitrification in cases of low C/N influents.

Elimination of NO/sub x/ by selective reduction with NH3

International Nuclear Information System (INIS)

Bruggeman, A.; Meynendonckx, L.; Gossens, W.R.A.

1979-01-01

In nuclear reprocessing plants the nitrogen oxides generated during the dissolution of the fuel are only partially removed in the primary off-gas treatments. Further reduction to the ppM level is necessary as a preliminary step to the cryogenic retention and separation of the noble gases. If simultaneous oxygen removal is not required, selective reduction of NO (and NO 2 ) to N 2 and H 2 O by NH 3 is a preferable method. Laboratory experiments have confrmed the feasibility of eliminating NO from air beyond the ppM level by adding NH 3 over a hydrogen mordenite catalyst. At atmospheric pressure and with air (water content 0.5% V/V) as a carrier gas selective catalytic reduction of NO to N 2 is easily achieved at temperatures up to 500 0 C. Under the same conditions dimensioning of the reactor for destruction of the excess NH 3 by the O 2 of the air is made possible. The activity of the catalyst remains rather constant even when large concentrations of I 2 are present. On the basis of the laboratory results a pilot installation has been designed and constructed which will demonstrate the process in an integrated gas purification loop at a pressure of 8 x 10 5 Pa during the next months

Simultaneous removal of sulfide, nitrate and acetate under denitrifying sulfide removal condition: Modeling and experimental validation

Energy Technology Data Exchange (ETDEWEB)

Xu, Xijun; Chen, Chuan; Wang, Aijie; Guo, Wanqian; Zhou, Xu [State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Lee, Duu-Jong, E-mail: djlee@ntu.edu.tw [State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Department of Chemical Engineering, National Taiwan University, Taipei 106, Taiwan (China); Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 106, Taiwan (China); Ren, Nanqi, E-mail: rnq@hit.edu.cn [State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Chang, Jo-Shu [Research Center for Energy Technology and Strategy, National Cheng Kung University, Tainan, Taiwan (China)

2014-01-15

Graphical abstract: Model evaluation applied to case study 1: (A-G) S{sup 2−}, NO{sub 3}{sup −}-N, NO{sub 2}{sup −}-N, and Ac{sup −}-C profiles under initial sulfide concentrations of 156.2 (A), 539 (B), 964 (C), 1490 (D), 342.7 (E), 718 (F), and 1140.7 (G) mg L{sup −1}. The solid line represents simulated result and scatter represents experimental result. -- Highlights: • This work developed a mathematical model for DSR process. • Kinetics of sulfur–nitrogen–carbon and interactions between denitrifiers were studied. • Kinetic parameters of the model were estimated via data fitting. • The model described kinetic behaviors of DSR processes over wide parametric range. -- Abstract: Simultaneous removal of sulfide (S{sup 2−}), nitrate (NO{sub 3}{sup −}) and acetate (Ac{sup −}) under denitrifying sulfide removal process (DSR) is a novel biological wastewater treatment process. This work developed a mathematical model to describe the kinetic behavior of sulfur–nitrogen–carbon and interactions between autotrophic denitrifiers and heterotrophic denitrifiers. The kinetic parameters of the model were estimated via data fitting considering the effects of initial S{sup 2−} concentration, S{sup 2−}/NO{sub 3}{sup −}-N ratio and Ac{sup −}-C/NO{sub 3}{sup −}-N ratio. Simulation supported that the heterotrophic denitratation step (NO{sub 3}{sup −} reduction to NO{sub 2}{sup −}) was inhibited by S{sup 2−} compared with the denitritation step (NO{sub 2}{sup −} reduction to N{sub 2}). Also, the S{sup 2−} oxidation by autotrophic denitrifiers was shown two times lower in rate with NO{sub 2}{sup −} as electron acceptor than that with NO{sub 3}{sup −} as electron acceptor. NO{sub 3}{sup −} reduction by autotrophic denitrifiers occurs 3–10 times slower when S{sup 0} participates as final electron donor compared to the S{sup 2−}-driven pathway. Model simulation on continuous-flow DSR reactor suggested that the adjustment of

Selective Catalytic Reduction of NO with NH3 Over V-MCM-41 Catalyst.

Science.gov (United States)

Kwon, Woo Hyun; Park, Sung Hoon; Kim, Ji Man; Park, Su Bin; Jung, Sang-Chul; Kim, Sang Chai; Jeon, Jong-Ki; Park, Young-Kwon

2016-02-01

V-MCM-41, a mesoporous catalyst doped with V2O5, was applied for the first time to the removal of atmospheric NO. The quantity of V2O5 added was 10 wt% and 30 wt%. The characteristics of the synthesized catalysts were examined using XRD, N2 soprtion, and NH3-TPD. With increasing quantity of V2O5 added, specific surface area decreased and pore size increased. When the quantity of V2O5 was 10 wt%, the MCM-41 structure was retained, whereas considerable collapse of mesoporous structure was observed when 30 wt% V2O5 was added. The examination of acid characteristics using NH3-TPD showed that 30 wt% V-MCM-41 had the higher NH3 adsorption ability, implying that it would exhibit high activity for NH3 SCR reaction. In the NO removal experiments, 30 wt% V-MCM-41 showed much higher NO removal efficiency than 10 wt% V-MCM-41, which was attributed to its high NH3 adsorption ability.

Thermodynamic modeling of Cl(-), NO3(-) and SO4(2-) removal by an anion exchange resin and comparison with Dubinin-Astakhov isotherms.

Science.gov (United States)

Dron, Julien; Dodi, Alain

2011-03-15

The removal of chloride, nitrate, and sulfate ions from wastewaters by a macroporous ion-exchange resin is studied through the experimental results obtained for six ion exchange systems, OH(-)/Cl(-), OH(-)/NO3(-), OH(-)/SO4(2-), and HCO3(-)/Cl(-), Cl(-)/NO3(-), Cl(-)/SO4(2-). The results are described through thermodynamic modeling, considering either an ideal or a nonideal behavior of the ionic species in the liquid and solid phases. The nonidealities are determined by the Davies equation and Wilson equations in the liquid and solid phases, respectively. The results show that the resin has a strong affinity for all the target ions, and the order of affinity obtained is OH(-) < HCO3(-) < Cl(-) < NO3(-) < SO4(2-). The calculation of the changes in standard Gibbs free energies (ΔG(0)) shows that even though HCO3(-) has a lower affinity to the resin, it may affect the removal of Cl(-), and in the same way that Cl(-) may affect the removal of NO3(-) and SO4(2-). The application of nonidealities in the thermodynamic model leads to an improved fit of the model to the experimental data with average relative deviations below 1.5% except for the OH(-)/SO4(2-) system. On the other hand, considering ideal or nonideal behaviors has no significant impact on the determination of the selectivity coefficients. The thermodynamic modeling is also compared with the Dubinin-Astakhov adsorption isotherms obtained for the same ion exchange systems. Surprisingly, the latter performs significantly better than the ideal thermodynamic model and nearly as well as the nonideal thermodynamic model.

Nitrogen uptake by wheat seedlings, interactive effects of four nitrogen sources: NO3-, NO2-, NH4+, and urea

Science.gov (United States)

Criddle, R. S.; Ward, M. R.; Huffaker, R. C.

1988-01-01

The net influx (uptake) rates of NO3-, NH4+, NO2-, and urea into roots of wheat (Triticum aestivum cv Yecora Rojo) seedlings from complete nutrient solutions containing all four compounds were monitored simultaneously. Although urea uptake was too slow to monitor, its presence had major inhibitory effects on the uptake of each of the other compounds. Rates of NO3-, NH4+, and NO2- uptake depended in a complex fashion on the concentration of all four N compounds. Equations were developed which describe the uptake rates of each of the compounds, and of total N, as functions of concentrations of all N sources. Contour plots of the results show the interactions over the range of concentrations employed. The coefficients of these equations provide quantitative values for evaluating primary and interactive effects of each compound on N uptake.

Towards environmentally sustainable aquaculture: Exploiting fermentation products from anaerobic sludge digestion for fueling nitrate removal in RAS

DEFF Research Database (Denmark)

Suhr, Karin Isabel; Pedersen, Per Bovbjerg

2011-01-01

is by production in recirculating aquaculture systems (RAS). In Denmark, more than 50 % of total fresh-water rainbow trout production is made in semi-intensive RAS, called ModelTroutFarms (MTF). MTF efficiently removes organic matter (93%), phosphorous (76%), and nitrogen (50%) (Svendsen et al., 2008). This makes...... being the final cleaning component of the MTF set-up. No specific denitrification filter has so far been implemented in Danish MTFs. An in-situ study was conducted at a commercial MTF (1000 ton/year) for evaluating the potential of using the fermentation products from anaerobic digestion in the sludge...... time (HRT) from 50 to 180 min. The highest removal rate recorded, 125 g NO3-N/m3reactor/d, was found in treatments at the design center point, and multivariate response surface analysis modeled a maximum N-removal at C/N ratio of 8.8 and HRT of 114 min. The effect of C/N ratio depended on the HRT...

Detachment of solid particulate soils by centrifugal force part 3; Properties of direction for removal force. Enshinryoku ni yoru ryushi yogore no jokyo. dai sanpo; Jokyoryoku no hokosei

Energy Technology Data Exchange (ETDEWEB)

Iwasaki, Y. (Koriyama Womens College, Fukushima (Japan)); Lee, S.H. (Tokyo Gakugei Univ., Tokyo (Japan)); Yabe, A. (Bunka Womens Univ., Tokyo (Japan))

1991-01-20

Removal by centrigugal force of polystyrene-latex particles with particle sizes of 5, 10 and 15 {mu} m adhering to a glass substrate is studied. Washing was carried out by using an ultracentrifuge provided with an angular rotor, with a rotor angle {theta} of 0 {approximately} 60 {degree}, varying the ratio of horizontal component Fh to vertical component Fv from 1:0 to 1:1.73. Washing was further carried out, changing an angle {theta}{prime} of centrifugal force to the surface on which the particles adhered. From this experiment, the following conclusions were obtained. The less the contribution of Fv to the constant Fh, or reversely the greater the contribution of Fh to the constant Fv, the more was the extent of removal. When the surface on which the particles adhered was turned to the direction pressed by centrifugal force, Fv acted negatively for removal of particles and exhibited a different tendency from that when turned to the the centrifugal direction. When {theta}{prime} was 180 {degree}, the removal force giving an extent of removal of about 80% was 1.5 {times} 10 {sup {minus} 9} N for 5 and 10 {mu} m particles, and 25 {times} 10 {sup {minus} 9} N for 15 {mu} m particles. 11 refs., 14 figs., 3 tabs.

RAPID NITRATE UPTAKE RATES AND LARGE SHORT-TERM STORAGE CAPACITIES MAY EXPLAIN WHY OPPORTUNISTIC GREEN MACROALGAE DOMINATE SHALLOW EUTROPHIC ESTUARIES1.

Science.gov (United States)

Kennison, Rachel L; Kamer, Krista; Fong, Peggy

2011-06-01

We quantified the effects of initial macroalgal tissue nitrogen (N) status (depleted and enriched) and varying pulses of nitrate (NO 3 - ) concentration on uptake and storage of nitrogen in Ulva intestinalis L. and Ulva expansa (Setch.) Setch. et N. L. Gardner using mesocosms modeling shallow coastal estuaries in Mediterranean climates. Uptake of NO 3 - (μmol · g dry weight [dwt] -1  · h -1 ) was measured as loss from the water after 1, 2, 4, 8, 12, and 24 h and storage as total tissue nitrogen (% dwt) and nitrate (ppm). Both species of algae exhibited a high affinity for NO 3 - across all N pulses and initial tissue contents. There was greater NO 3 - removal from the water for depleted than enriched algae across all time intervals. In the low-N-pulse treatment, U. intestinalis and U. expansa removed all measurable NO 3 - within 8 and 12 h, respectively, and in the medium and high treatments, removal was high and then decreased over time. Maximum mean uptake rates of nitrate were greater for U. expansa (∼300 μmol · g dwt -1  · h -1 ) than U. intestinalis (∼100 μmol · g dwt -1  · h -1 ); however, uptake rates were highly variable over time. Overall, U. expansa uptake rates were double those of U. intestinalis. Maximum tissue NO 3 - for U. expansa was >1,000 ppm, five times that of U. intestinalis, suggesting that U. expansa has a greater storage capacity in this cellular pool. These results showed that opportunistic green algae with differing tissue nutrient histories were able to efficiently remove nitrate from the water across a wide range of N pulses; thus, both are highly adapted to proliferate in estuarine environments with pulsed nutrient supplies. © 2011 Phycological Society of America.

Atmospheric chemistry of CF3CF═CH2 and (Z)-CF3CF═CHF: Cl and NO3 rate coefficients, Cl reaction product yields, and thermochemical calculations.

Science.gov (United States)

Papadimitriou, Vassileios C; Lazarou, Yannis G; Talukdar, Ranajit K; Burkholder, James B

2011-01-20

Rate coefficients, k, for the gas-phase reactions of Cl atoms and NO(3) radicals with 2,3,3,3-tetrafluoropropene, CF(3)CF═CH(2) (HFO-1234yf), and 1,2,3,3,3-pentafluoropropene, (Z)-CF(3)CF═CHF (HFO-1225ye), are reported. Cl-atom rate coefficients were measured in the fall-off region as a function of temperature (220-380 K) and pressure (50-630 Torr; N(2), O(2), and synthetic air) using a relative rate method. The measured rate coefficients are well represented by the fall-off parameters k(0)(T) = 6.5 × 10(-28) (T/300)(-6.9) cm(6) molecule(-2) s(-1) and k(∞)(T) = 7.7 × 10(-11) (T/300)(-0.65) cm(3) molecule(-1) s(-1) for CF(3)CF═CH(2) and k(0)(T) = 3 × 10(-27) (T/300)(-6.5) cm(6) molecule(-2) s(-1) and k(∞)(T) = 4.15 × 10(-11) (T/300)(-0.5) cm(3) molecule(-1) s(-1) for (Z)-CF(3)C═CHF with F(c) = 0.6. Reaction product yields were measured in the presence of O(2) to be (98 ± 7)% for CF(3)C(O)F and (61 ± 4)% for HC(O)Cl in the CF(3)CF═CH(2) reaction and (108 ± 8)% for CF(3)C(O)F and (112 ± 8)% for HC(O)F in the (Z)-CF(3)CF═CHF reaction, where the quoted uncertainties are 2σ (95% confidence level) and include estimated systematic errors. NO(3) reaction rate coefficients were determined using absolute and relative rate methods. Absolute measurements yielded upper limits for both reactions between 233 and 353 K, while the relative rate measurements yielded k(3)(295 K) = (2.6 ± 0.25) × 10(-17) cm(3) molecule(-1) s(-1) and k(4)(295 K) = (4.2 ± 0.5) × 10(-18) cm(3) molecule(-1) s(-1) for CF(3)CF═CH(2) and (Z)-CF(3)CF═CHF, respectively. The Cl-atom reaction with CF(3)CF═CH(2) and (Z)-CF(3)CF═CHF leads to decreases in their atmospheric lifetimes and global warming potentials and formation of a chlorine-containing product, HC(O)Cl, for CF(3)CF═CH(2). The NO(3) reaction has been shown to have a negligible impact on the atmospheric lifetimes of CF(3)CF═CH(2) and (Z)-CF(3)CF═CHF. The energetics for the reaction of Cl, NO(3), and OH with CF

[Isolation, Identification and Nitrogen Removal Characteristics of a Heterotrophic Nitrification-Aerobic Denitrification Strain y3 Isolated from Marine Environment].

Science.gov (United States)

Sun, Qing-hua; Yu, De-shuang; Zhang, Pei-yu; Lin, Xue-zheng; Xu, Guang-yao; Li, Jin

2016-03-15

A heterotrophic nitrification--aerobic denitrification bacterium named y3 was isolated from the sludge of Jiaozhou Bay using the enrichment medium with seawater as the matrix. It was identified as Pseudomonas sp. based on the morphological observation, physiological experiments and sequence analysis of 16S rRNA. The experiment results showed that the optimal carbon resource was sodium citrate, the optimal pH was 7.0, and the optimal C/N was 13. The strain could use NH₄Cl, NaNO₂ and KNO₃ as sole nitrogen source, and the removal efficiencies were 98.69%, 78.38% and 72.95% within 20 hours, respectively. There was no nitrate and nitrite accumulation during the heterotrophic nitrification process. Within 20 hours, the nitrogen removal efficiencies were 99.56%, 99.75% and 99.41%, respectively, in the mixed system with NO₃⁻-N: NO²⁻-N of 2:1, 1:1 and 1:2. When the NH₄⁺-N: NO₃⁻-N ratios were 2: 1 , 1: 1 , 1: 2, the nitrogen removal efficiencies were all 100% . When the NH₄⁺-N:NO₂⁻-N ratios were 2:1,1:1,1:2, the nitrogen removal efficiencies were 90.43%, 92.79% and 99.96%, respectively. They were higher than those with single nitrogen source. As a result, strain y3 had good nitrogen removal performance in high saline wastewater treatment.

ELIMINACIÓN DE COLORANTES CATIÓNICOS USANDO OZONO, ZEOLITA NATURAL Y OZONO/ZEOLITA CATIONIC DYES REMOVAL USING OZONE, NATURAL ZEOLITE, AND OZONE/ZEOLITE

Directory of Open Access Journals (Sweden)

Héctor Valdés

2009-12-01

Full Text Available En este trabajo se comparan resultados experimentales de remoción azul de metileno (MB utilizando tratamientos basados en la oxidación con ozono (O3, la adsorción con zeolita natural (ZN, y tratamiento simultáneo de adsorción y oxidación con ozono en presencia de zeolita natural (O3/ZN. Se evalúa, a escala de laboratorio, el efecto del pH (2-8 y la presencia de sustancias atrapadoras radicales libres (iones acetatos en la velocidad de remoción y en la eficiencia de los procesos. Los experimentos se realizaron en un reactor diferencial compuesto por un estanque de 1 dm³ y una columna de 19 cm³ de capacidad. El ozono fue generado a razón de 5 g O3/h. Los resultados mostraron que el sistema simultáneo de oxidación/adsorción O3/ZN incrementa la velocidad de remoción del MB con respecto a los procesos separados de ozonización y adsorción con zeolita. En presencia de sustancias atrapadoras de radicales, se observó un 70% de disminución en la velocidad de remoción de MB cuando se empleó el tratamiento con O3 y sólo un 25% cuando se utiliza el tratamiento combinado O3/ZN. Los resultados sugieren que la reacción de oxidación del MB en el sistema tiene lugar fundamentalmente sobre la superficie de la zeolita.This paper compares experimental results on methylene blue (MB removal systems based on ozone oxidation, zeolite adsorption, and simultaneous adsorption-oxidation using ozone in the presence of natural zeolite. The effect of pH (2-8, and the presence of radical scavengers (sodium acetate on process rates and removal efficiencies are assessed at laboratory scale. The experimental system consisted of a 1L differential circular flow reactor and an ozone generator rated at 5 g O3/h. Results show that ozone oxidation combined with zeolite adsorption increases the overall MB oxidation rate with respect to ozonation process and zeolite adsorption. In presence of free radical scavenger, only a 25% of reduction on MB removal rate are

Application of subsurface wastewater infiltration system to on-site treatment of domestic sewage under high hydraulic loading rate

Directory of Open Access Journals (Sweden)

Ying-hua Li

2015-01-01

Full Text Available In order to enhance the hydraulic loading rate (HLR of a subsurface wastewater infiltration system (SWIS used in treating domestic sewage, the intermittent operation mode was employed in the SWIS. The results show that the intermittent operation mode contributes to the improvement of the HLR and the pollutant removal rate. When the wetting-drying ratio (RWD was 1.0, the pollutant removal rate increased by (13.6 ± 0.3% for NH3-N, (20.7 ± 1.1% for TN, (18.6 ± 0.4% for TP, (12.2 ± 0.5% for BOD, (10.1 ± 0.3% for COD, and (36.2 ± 1.2% for SS, compared with pollutant removal rates under the continuous operation mode. The pollutant removal rate declined with the increase of the HLR. The effluent quality met The Reuse of Urban Recycling Water – Water Quality Standard for Scenic Environment Use (GB/T 18921-2002 even when the HLR was as high as 10 cm/d. Hydraulic conductivity, oxidation reduction potential (ORP, the quantity of nitrifying bacteria, and the pollutant removal rate of NH3-N increased with the decrease of the RWD. For the pollutant removal rates of TP, BOD, and COD, there were no significant difference (p < 0.05 under different RWDs. The suggested RWD was 1.0. Relative contribution of the pretreatment and SWIS to the pollutant removal was examined, and more than 80% removal of NH3-N, TN, TP, COD, and BOD occurred in the SWIS.

Application of response surface methodology (RSM) for optimisation of COD, NH3-N and 2,4-DCP removal from recycled paper wastewater in a pilot-scale granular activated carbon sequencing batch biofilm reactor (GAC-SBBR).

Science.gov (United States)

Muhamad, Mohd Hafizuddin; Sheikh Abdullah, Siti Rozaimah; Mohamad, Abu Bakar; Abdul Rahman, Rakmi; Hasan Kadhum, Abdul Amir

2013-05-30

In this study, the potential of a pilot-scale granular activated carbon sequencing batch biofilm reactor (GAC-SBBR) for removing chemical oxygen demand (COD), ammoniacal nitrogen (NH3-N) and 2,4-dichlorophenol (2,4-DCP) from recycled paper wastewater was assessed. For this purpose, the response surface methodology (RSM) was employed, using a central composite face-centred design (CCFD), to optimise three of the most important operating variables, i.e., hydraulic retention time (HRT), aeration rate (AR) and influent feed concentration (IFC), in the pilot-scale GAC-SBBR process for recycled paper wastewater treatment. Quadratic models were developed for the response variables, i.e., COD, NH3-N and 2,4-DCP removal, based on the high value (>0.9) of the coefficient of determination (R(2)) obtained from the analysis of variance (ANOVA). The optimal conditions were established at 750 mg COD/L IFC, 3.2 m(3)/min AR and 1 day HRT, corresponding to predicted COD, NH3-N and 2,4-DCP removal percentages of 94.8, 100 and 80.9%, respectively. Copyright © 2013 Elsevier Ltd. All rights reserved.

Effect of dissolved oxygen on nitrogen removal and process control in aerobic granular sludge reactor

International Nuclear Information System (INIS)

Yuan Xiangjuan; Gao Dawen

2010-01-01

A sequencing batch reactor (SBR) with aerobic granular sludge was operated to determine the effect of different DO concentrations on biological nitrogen removal process and to investigate the spatial profiles of DO, ORP and pH as online control parameters in such systems. The results showed that DO concentration had a significant effect on nitrification efficiencies and the profiles of DO, ORP and pH. The specific nitrification rate was decreased from 0.0595 mgNH 4 + -N/(gMLSS min) to 0.0251 mgNH 4 + -N/(gMLSS min) after DO concentration was dropped off from 4.5 mg/L to 1.0 mg/L. High DO concentration improved the nitrification and increased the volumetric NH 4 + -N removal. Low DO concentration enhanced TIN removal, while prolonged the nitrification duration. Also there existed a good correlation between online control parameters (ORP, pH) and nutrient (COD, NH 4 + -N, NO 2 - -N, NO 3 - -N) variations in aerobic granular sludge reactor when DO was 2.5 mg/L, 3.5 mg/L and 4.5 mg/L. However it was difficult to identify the end of nitrification and denitrification when DO was 1.0 mg/L, due to no apparent bending points on ORP and pH curves. In conclusion, the optimal DO concentration was suggested at 2.5 mg/L as it not only achieved high nitrogen removal efficiency and decreased the reaction duration, but also saved operation cost by aeration and mixing.

Comparison of Four Nitrate Removal Kinetic Models in Two Distinct Wetland Restoration Mesocosm Systems

Directory of Open Access Journals (Sweden)

Tiffany L. Messer

2017-07-01

Full Text Available The objective of the study was to determine the kinetic model that best fit observed nitrate removal rates at the mesocosm scale in order to determine ideal loading rates for two future wetland restorations slated to receive pulse flow agricultural drainage water. Four nitrate removal models were investigated: zero order, first order decay, efficiency loss, and Monod. Wetland mesocosms were constructed using the primary soil type (in triplicate at each of the future wetland restoration sites. Eighteen mesocosm experiments were conducted over two years across seasons. Simulated drainage water was loaded into wetlands as batches, with target nitrate-N levels typically observed in agricultural drainage water (between 2.5 and 10 mg L−1. Nitrate-N removal observed during the experiments provided the basis for calibration and validation of the models. When the predictive strength of each of the four models was assessed, results indicated that the efficiency loss and first order decay models provided the strongest agreement between predicted and measured NO3-N removal rates, and the fit between the two models were comparable. Since the predictive power of these two models were similar, the less complicated first order decay model appeared to be the best choice in predicting appropriate loading rates for the future full-scale wetland restorations.

Aerobic granules formation and nutrients removal characteristics in sequencing batch airlift reactor (SBAR) at low temperature

International Nuclear Information System (INIS)

Bao Ruiling; Yu Shuili; Shi Wenxin; Zhang Xuedong; Wang Yulan

2009-01-01

To understand the effect of low temperature on the formation of aerobic granules and their nutrient removal characteristics, an aerobic granular sequencing batch airlift reactor (SBAR) has been operated at 10 deg. C using a mixed carbon source of glucose and sodium acetate. The results showed that aerobic granules were obtained and that the reactor performed in stable manner under the applied conditions. The granules had a compact structure and a clear out-surface. The average parameters of the granules were: diameter 3.4 mm, wet density 1.036 g mL -1 , sludge volume index 37 mL g -1 , and settling velocity 18.6-65.1 cm min -1 . Nitrite accumulation was observed, with a nitrite accumulation rate (NO 2 - -N/NO x - -N) between 35% and 43% at the beginning of the start-up stage. During the stable stage, NO x was present at a level below the detection limit. However, when the influent COD concentration was halved (resulting in COD/N a reduction of the COD/N from 20:1 to 10:1) nitrite accumulation was observed once more with an effluent nitrite accumulation rate of 94.8%. Phosphorus release was observed in the static feeding phase and also during the initial 20-30 min of the aerobic phase. Neither the low temperature nor adjustment of the COD/P ratio from 100:1 to 25:1 had any influence on the phosphorus removal efficiency under the operating conditions. In the granular reactor with the influent load rates for COD, NH 4 + -N, and PO 4 3- -P of 1.2-2.4, 0.112 and 0.012-0.024 kg m -3 d -1 , the respective removal efficiencies at low temperature were 90.6-95.4%, 72.8-82.1% and 95.8-97.9%.

Fabrication of conductive and high-dispersed Ppy@Ag/g-C{sub 3}N{sub 4} composite photocatalysts for removing various pollutants in water

Energy Technology Data Exchange (ETDEWEB)

Zhu, Zhi; Tang, Xu [School of Chemistry and Chemical Engineering, Jiangsu University (China); Ma, Changchang [School of the Environment and Safety Engineering, Jiangsu University (China); Song, Minshan [School of Mathematics and Physics, Jiangsu University of Science and Technology (China); Gao, Nailing; Wang, Youshan; Huo, Pengwei [School of Chemistry and Chemical Engineering, Jiangsu University (China); Lu, Ziyang, E-mail: mrzhuzhi007@163.com [School of the Environment and Safety Engineering, Jiangsu University (China); Yan, Yongsheng, E-mail: gchxz206@126.com [School of Chemistry and Chemical Engineering, Jiangsu University (China)

2016-11-30

Highlights: • The high-dispersed Ag modified g-C{sub 3}N{sub 4} (Ag/g-C{sub 3}N{sub 4}) was successfully synthesized in situ deposited on the surface of g-C{sub 3}N{sub 4} during calcined melamine. • The as-prepared Ppy@Ag/g-C{sub 3}N{sub 4} could remove of various organic pollutants in water. • The enhanced photocatalytic activity of Ppy@Ag/g-C{sub 3}N{sub 4} comes from π conjugated electronic structures of Ppy and Ag species as the electron transfer mediator between Ppy and g-C{sub 3}N{sub 4}. • The Ppy@Ag/g-C{sub 3}N{sub 4} sample also showed a relatively good recycling stability. - Abstract: The ternary conductive Ppy@Ag/g-C{sub 3}N{sub 4} composite photocatalysts was successfully synthesized by polymerization process and surface polymerization technique. And the as-prepared Ppy@Ag/g-C{sub 3}N{sub 4} sample exhibited the higher photocatalytic activity for various pollutant (MO, DM, TC, CIP, GFLX and EH) remove than that of pure g-C{sub 3}N{sub 4} and Ag/g-C{sub 3}N{sub 4} under visible light irradiation. It mainly originated from the Ag nanoparticles anchored between g-C{sub 3}N{sub 4} and Ppy acted as electron transfer mediator that facilitated the charge carrier separation and then expending the lifetime of the carriers. Meanwhile, the obtained Ppy@Ag/g-C{sub 3}N{sub 4} sample also showed a relatively good recycling stability which was the crucial factor for photocatalyst practical application. This work provided a new facile strategy for improving photo-degradation activity of g-C{sub 3}N{sub 4} photocatalyst.

Absolute rate constants for the reaction of CF3O2 and CF3O radicals with NO at 295 K

DEFF Research Database (Denmark)

Sehested, J.; Nielsen, O.J.

1993-01-01

Using a pulse radiolysis UV absorption technique and subsequent simulations of experimental NO2 and FNO absorption transients, rate constants for reaction between CF3O and CF3O2 radicals with NO were determined, CF3O2+NO-->CF3O+NO2 (3), CF3O+NO-->CF2O+FNO (5). k3 was derived to be (1.68+/-0.26)x10...

Performance of slow rate systems for treatment of domestic wastewater.

Science.gov (United States)

Tzanakakis, V E; Paranychianakis, N V; Angelakis, A N

2007-01-01

The performance of slow rate (SR) systems in terms of treatment efficiency, environmental and health risks, and land sustainability was investigated over a three-year period in a rural community close to Iraklio, Greece. Four plant species (Acacia cyanophylla, Eucalyptus camandulensis, Populus nigra and Arundo donax) were used in order to investigate the role of vegetation in the treatment of wastewater and in biomass production. Wastewater effluent was pre-treated in a septic tank before its application to land. Applied hydraulic loading rates were based on crop water requirements which were determined separately for each plant species. The evaluation of treatment performance was accomplished by measuring COD, TKN, NH3-N, NO3-N, total and reactive P, TC and FC in soil solution samples taken at different depths (15, 30 and 60 cm). SR systems showed great potential for COD, TKN and NH4-N removal which reached 89, 90 and 94%, respectively at a depth of 15 cm. An outstanding removal was also observed for TC and FC which reached 99.99%. The concentration of both P and NO3-N in soil solution increased with the passage of time, but it was lower in winter. Despite the differences in the application rates among the SR systems planted with different plant species, the treatment efficiency was not affected. Moreover, increasing the soil depth from 15 to 60 cm had no effect on the treatment efficiency of the SR systems.

Synthesis, characterization and photocatalytic activity of WO{sub 3}/TiO{sub 2} for NO removal under UV and visible light irradiation

Energy Technology Data Exchange (ETDEWEB)

Luévano-Hipólito, E. [CIIDIT, Facultad de Ingeniería Mecánica y Eléctrica, Universidad Autónoma de Nuevo León, Ciudad Universitaria, C.P. 66451 San Nicolás de los Garza, N.L. (Mexico); Martínez-de la Cruz, A., E-mail: azael.martinezdl@uanl.edu.mx [CIIDIT, Facultad de Ingeniería Mecánica y Eléctrica, Universidad Autónoma de Nuevo León, Ciudad Universitaria, C.P. 66451 San Nicolás de los Garza, N.L. (Mexico); López-Cuellar, E. [CIIDIT, Facultad de Ingeniería Mecánica y Eléctrica, Universidad Autónoma de Nuevo León, Ciudad Universitaria, C.P. 66451 San Nicolás de los Garza, N.L. (Mexico); Yu, Q.L.; Brouwers, H.J.H. [Department of the Built Environment, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven (Netherlands)

2014-11-14

Samples with different proportions WO{sub 3}/TiO{sub 2} were prepared by co-precipitation method followed by a heat treatment. The samples were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance spectroscopy (DRS), and adsorption–desorption N{sub 2} isotherms (BET). The photocatalytic properties of WO{sub 3}/TiO{sub 2} samples were evaluated in the photo-oxidation reaction of nitric oxide (NO) under UV and visible light irradiation. The highest photocatalytic activity was observed in the WO{sub 3}/TiO{sub 2} sample with a composition of 80% mole of TiO{sub 2}. Among the different substrates used for supporting the photocatalyst, the best results were reached over concrete and glass when it was exposed to UV and visible light irradiation, respectively. In overall, the photocatalytic efficiency of the synthesized materials was higher under UV than visible light irradiation. - Highlights: • WO{sub 3}/TiO{sub 2} prepared in simple way show high photocatalytic activity for NO removal. • The concrete was the best substrate to the performance of WO{sub 3}/TiO{sub 2} with UV radiation. • The glass was the best substrate to the performance of WO{sub 3}/TiO{sub 2} with visible radiation.

Removal of nitrite impurity from nitrate labeled with nitrogen-15

International Nuclear Information System (INIS)

Malone, J.P.; Stevens, R.J.

1998-01-01

Potassium nitrate labeled with 15 N is often used as a tracer in studies of N dynamics in soil and water systems. Typically, 0.8% NO 2 - impurity has been found in the batches of K 15 NO 3 enriched to 99 atom % excess 15 N that were purchased by our laboratory. Nitrite is an intermediate in several N cycling processes so its addition when adding NO 3 - could produce misleading results. We have developed a safe, simple, and inexpensive method to remove NO 2 - impurity from any NO 3 - solution in a water matrix. The principle is the oxidation of NO2- to NO 3 - by UV light in the presence of a heterogenous TiO 2 catalyst. A NO 2 - concentration of 0.2 mM in 100 mL of 0.2 M NO 3 - solution could be oxidized in 12 min using 0.5 g L -1 TiO 2 in a specially constructed photoreactor with a 75-W UV facial tanning lamp. For the routine removal of NO 2 - , use of the same TiO 2 concentration in a standard beaker worked equally well when the irradiation time was extended to 2.5 h. After irradiation, the TiO2 is easily and totally removed from the solution by membrane filtration. (author)

Physicochemical properties of metal-doped activated carbons and relationship with their performance in the removal of SO2 and NO

International Nuclear Information System (INIS)

Gao Xiang; Liu Shaojun; Zhang Yang; Luo Zhongyang; Cen Kefa

2011-01-01

Research highlights: → Cu and Fe were partly reduced by carbon during preparation. → Metal-involved SO 2 removal pathways were catalytic oxidation, reaction and adsorption. → Good performances of SO 2 and NO removal depended on the metal redox pairs. - Abstract: Several metal-doped activated carbons (Fe, Co, Ni, V, Mn, Cu and Ce) were prepared and characterized. The results of N 2 adsorption-desorption, X-ray diffraction, and X-ray photoelectron spectroscopy indicated that some metals (Cu and Fe) were partly reduced by carbon during preparation. Activity tests for the removal of SO 2 and the selective catalytic reduction of NO with ammonia were carried out. Due to different physicochemical properties, different pathways for the SO 2 removal had been put out, i.e., catalytic oxidation, direct reaction and adsorption. This classification depended on the standard reduction potentials of metal redox pairs. Samples impregnated with V, Ce and Cu showed good activity for NO reduction by NH 3 , which was also ascribed to the reduction potential values of metal redox pairs. Ce seemed to be a promising alternative to V due to the higher activity in NO reduction and the nontoxic property. A metal cation which could easily convert between the two valences seemed to be crucial to the good performance of both SO 2 and NO removal, just like V and Cu.

Biomolecule-controlled hydrothermal synthesis of C-N-S-tridoped TiO2 nanocrystalline photocatalysts for NO removal under simulated solar light irradiation.

Science.gov (United States)

Wang, Yawen; Huang, Yu; Ho, Wingkei; Zhang, Lizhi; Zou, Zhigang; Lee, Shuncheng

2009-09-30

In this study, C-N-S-tridoped titanium dioxide (TiO(2)) nanocrystals were synthesized by using a facile hydrothermal method in the presence of a biomolecule l-cysteine. This biomolecule could not only serve as the common source for the carbon, sulfur and nitrogen tridoping, but also could control the final crystal phases and morphology. The resulting materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption and UV-vis diffuse reflectance spectroscopy. XPS analysis revealed that S was incorporated into the lattice of TiO(2) through substituting oxygen atoms, N might coexist in the forms of N-Ti-O and Ti-O-N in tridoped TiO(2) and most C could form a mixed layer of carbonate species deposited on the surface of TiO(2) nanoparticles. The photocatalytic activities of the samples were tested on the removal of NO at typical indoor air level in a flow system under simulated solar light irradiation. The tridoped TiO(2) samples showed much higher removal efficiency than commercial P25 and the undoped counterpart photocatalyst. The enhanced visible light photocatalytic activity of C-N-S-tridoped TiO(2) nanocrystals was explained on the basis of characterizations. The possible formation process of the monodispersed C-N-S-tridoped anatase TiO(2) nanocrystals was also proposed. This study provides a new method to prepare visible light active TiO(2) photocatalyst.

Biomolecule-controlled hydrothermal synthesis of C-N-S-tridoped TiO2 nanocrystalline photocatalysts for NO removal under simulated solar light irradiation

International Nuclear Information System (INIS)

Wang Yawen; Huang Yu; Ho Wingkei; Zhang Lizhi; Zou Zhigang; Lee Shuncheng

2009-01-01

In this study, C-N-S-tridoped titanium dioxide (TiO 2 ) nanocrystals were synthesized by using a facile hydrothermal method in the presence of a biomolecule L-cysteine. This biomolecule could not only serve as the common source for the carbon, sulfur and nitrogen tridoping, but also could control the final crystal phases and morphology. The resulting materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption and UV-vis diffuse reflectance spectroscopy. XPS analysis revealed that S was incorporated into the lattice of TiO 2 through substituting oxygen atoms, N might coexist in the forms of N-Ti-O and Ti-O-N in tridoped TiO 2 and most C could form a mixed layer of carbonate species deposited on the surface of TiO 2 nanoparticles. The photocatalytic activities of the samples were tested on the removal of NO at typical indoor air level in a flow system under simulated solar light irradiation. The tridoped TiO 2 samples showed much higher removal efficiency than commercial P25 and the undoped counterpart photocatalyst. The enhanced visible light photocatalytic activity of C-N-S-tridoped TiO 2 nanocrystals was explained on the basis of characterizations. The possible formation process of the monodispersed C-N-S-tridoped anatase TiO 2 nanocrystals was also proposed. This study provides a new method to prepare visible light active TiO 2 photocatalyst.

Study of a combined heterotrophic and sulfur autotrophic denitrification technology for removal of nitrate in water

International Nuclear Information System (INIS)

Liu Huijuan; Jiang Wei; Wan Dongjin; Qu Jiuhui

2009-01-01

A combined two-step process of heterotrophic denitrification in a fluidized reactor and sulfur autotrophic denitrification processes (CHSAD) was developed for the removal of nitrate in drinking water. In this process, the advantage of high efficiency of heterotrophic denitrification with non-excessive methanol and the advantage of non-pollution of sulfur autotriphic denitrification were integrated in this CHSAD process. And, this CHSAD process had the capacity of pH balance and could control the concentration of SO 4 2- in effluent by adjusting the operation condition. When the influent nitrate was 30 mg NO 3 - -N/L, the reactor could be operated efficiently at the hydraulic retention time (HRT) ranging from 20 to 40 min with C:N ratio (mg CH 3 OH:mg NO 3 - -N) of 2.0 (methanol as carbon source). The nitrate removal was nearly 100% and there was no accumulated nitrite or residual methanol in the effluent. The effluent pH was about 7.5 and the sulfate concentration was lower than 130 mg/L. The maximum volume-loading rate of the reactor was 2.16 kg NO 3 - -N/(m 3 d). The biomass and scanning electron microscopy graphs of biofilm were also analyzed.

Comparison of recirculation configurations for biological nutrient removal in a membrane bioreactor.

Science.gov (United States)

Bekir Ersu, Cagatayhan; Ong, Say Kee; Arslankaya, Ertan; Brown, Patrick

2008-03-01

A 12-L lab-scale membrane bioreactor (MBR), consisting of an anaerobic and anoxic compartment followed by an oxic plate-frame membrane compartment, was evaluated for carbonaceous and nutrient removals by varying the recirculation of mixed liquor and permeate. The hydraulic retention times (HRTs) for the anaerobic, anoxic, and oxic compartments were 2, 2, and 8h, respectively. The solids residence time (SRT) for the oxic compartment was 25 days. Five different recirculation configurations were tested by recirculating mixed liquor and/or permeate recirculation equal to the influent flow rate (identified as 100%) into different locations of the anaerobic and anoxic compartments. Of the five configurations, the configuration with 100% mixed liquor recirculation to the anaerobic compartment and 100% permeate recirculation to the anoxic compartment gave the highest percentage removal with an average 92.3+/-0.5% soluble chemical oxygen demand (sCOD), 75.6+/-0.4% total nitrogen (TN), and 62.4+/-1.3% total phosphorus (TP) removal. When the mixed liquor and permeate recirculation rates were varied for the same configuration, the highest TP removal was obtained for 300% mixed liquor recirculation and 100% permeate recirculation (300%/100%) with a TP removal of 88.1+/-1.3% while the highest TN removal (90.3+/-0.3%) was obtained for 200%/300% recirculation. TN and TP concentrations as low as 4.2+/-0.1 and 1.4+/-0.2mg/L respectively were obtained. Mass loading rates were generally low in the range of 0.11-0.22kgCOD/kgMLSS/d due to high biomass concentrations within the oxic reactor (approx. 8000mg/L). The BioWin model was calibrated against one set of the experimental data and was found to predict the experimental data of effluent TN, TP, and NO(3)(-)-N but over-predicted sCOD and NH(3)-N for various recirculation rates. The anoxic heterotrophic yield for the calibrated model was 0.2kg biomass COD/kg COD utilized while the maximum growth rates were found to be 0.45day(-1) for mu

Nitrate removal from agricultural drainage ditch sediments with amendments of organic carbon: Potential for an innovative best management practice

Science.gov (United States)

Faust, Derek R.; Kröger, Robert; Miranda, Leandro E.; Rush, Scott A.

2016-01-01

Agricultural fertilizer applications have resulted in loading of nutrients to agricultural drainage ditches in the Lower Mississippi Alluvial Valley. The purpose of this study was to determine effects of dissolved organic carbon (DOC) and particulate organic carbon (POC) amendments on nitrate-nitrogen (NO3−-N) removal from overlying water, pore water, and sediment of an agricultural drainage ditch. Two experiments were conducted. In experiment 1, control (i.e., no amendment), DOC, and POC treatments were applied in laboratory microcosms for time intervals of 3, 7, 14, and 28 days. In experiment 2, control, DOC, and POC treatments were applied in microcosms at C/N ratios of 5:1, 10:1, 15:1, and 20:1. There were statistically significant effects of organic carbon amendments in experiment 1 (F2,71 = 27.1, P < 0.001) and experiment 2 (F2,53 = 39.1, P < 0.001), time (F1,71 = 14.5, P < 0.001) in experiment 1, and C/N ratio (F1,53 = 36.5, P < 0.001) in experiment 2. NO3−-N removal varied from 60 to 100 % in overlying water among all treatments. The lowest NO3−-N removals in experiment 1 were observed in the control at 14 and 28 days, which were significantly less than in DOC and POC 14- and 28-day treatments. In experiment 2, significantly less NO3−-N was removed in overlying water of the control compared to DOC and POC treatments at all C/N ratios. Amendments of DOC and POC made to drainage ditch sediment: (1) increased NO3−-N removal, especially over longer time intervals (14 to 28 days); (2) increased NO3−-N removal, regardless of C/N ratio; and (3) NO3−-N removal was best at a 5:1 C/N ratio. This study provides support for continued investigation on the use of organic carbon amendments as a best management practice for NO3−-N removal in agricultural drainage ditches.

Whole house particle removal and clean air delivery rates for in-duct and portable ventilation systems.

Science.gov (United States)

Macintosh, David L; Myatt, Theodore A; Ludwig, Jerry F; Baker, Brian J; Suh, Helen H; Spengler, John D

2008-11-01

A novel method for determining whole house particle removal and clean air delivery rates attributable to central and portable ventilation/air cleaning systems is described. The method is used to characterize total and air-cleaner-specific particle removal rates during operation of four in-duct air cleaners and two portable air-cleaning devices in a fully instrumented test home. Operation of in-duct and portable air cleaners typically increased particle removal rates over the baseline rates determined in the absence of operating a central fan or an indoor air cleaner. Removal rates of 0.3- to 0.5-microm particles ranged from 1.5 hr(-1) during operation of an in-duct, 5-in. pleated media filter to 7.2 hr(-1) for an in-duct electrostatic air cleaner in comparison to a baseline rate of 0 hr(-1) when the air handler was operating without a filter. Removal rates for total particulate matter less than 2.5 microm in aerodynamic diameter (PM2.5) mass concentrations were 0.5 hr(-1) under baseline conditions, 0.5 hr(-1) during operation of three portable ionic air cleaners, 1 hr(-1) for an in-duct 1-in. media filter, 2.4 hr(-1) for a single high-efficiency particle arrestance (HEPA) portable air cleaner, 4.6 hr(-1) for an in-duct 5-in. media filter, 4.7 hr(-1) during operation of five portable HEPA filters, 6.1 hr(-1) for a conventional in-duct electronic air cleaner, and 7.5 hr(-1) for a high efficiency in-duct electrostatic air cleaner. Corresponding whole house clean air delivery rates for PM2.5 attributable to the air cleaner independent of losses within the central ventilation system ranged from 2 m3/min for the conventional media filter to 32 m3/min for the high efficiency in-duct electrostatic device. Except for the portable ionic air cleaner, the devices considered here increased particle removal indoors over baseline deposition rates.

Ultrasound assisted synthesis of heterogeneous g-C{sub 3}N{sub 4}/BiVO{sub 4} composites and their visible-light-induced photocatalytic oxidation of NO in gas phase

Energy Technology Data Exchange (ETDEWEB)

Ou, Man; Zhong, Qin, E-mail: zq304@mail.njust.edu.cn; Zhang, Shule; Yu, Lemeng

2015-03-25

Highlights: • The g-C{sub 3}N{sub 4}/BiVO{sub 4} composites were prepared via ultrasonic and calcination methods. • The conversion of NO of G6B4 was 4 times larger than that of the pure phases. • There were only NO{sub 2}{sup −} and NO{sub 3}{sup −} produced in the PCO reaction process. • The promotional mechanism on the g-C{sub 3}N{sub 4}/BiVO{sub 4} heterojunctions was proposed. - Abstract: The visible light active g-C{sub 3}N{sub 4}/BiVO{sub 4} catalysts were synthesized via facile ultrasonic dispersion and calcination methods and used in the study for photocatalytic oxidation (PCO) of NO in gas phase. The as-synthesized samples were analyzed by various characterization techniques. The results exhibited that an interaction between BiVO{sub 4} and g-C{sub 3}N{sub 4} was confirmed and a heterojunction was formed on the surface of g-C{sub 3}N{sub 4}/BiVO{sub 4} composite, which enhanced the separation and transfer of photogenerated electron–hole pairs. The mechanism on the heterojunction effect to improve the PCO ability was also proposed. The activity test showed that the optimum content of g-C{sub 3}N{sub 4} was 50 wt%. And the maximum conversion of NO was four times larger than that of the pure components when the inlet concentration of NO was about 400 ppm under the visible light (VL) irradiation. The ion chromatography (IC) showed that NO was removed in the oxidation formation of NO{sub 2}{sup −} and NO{sub 3}{sup −}.

Tetracycline removal during wastewater treatment in high-rate algal ponds

International Nuclear Information System (INIS)

Godos, Ignacio de; Muñoz, Raúl; Guieysse, Benoit

2012-01-01

Highlights: ► Tetracycline removal was most likely caused by photodegradation and biosorption. ► Tetracycline presence was linked to biomass deflocculation and poor settleability. ► Deflocculation did not impact treatment efficiency. ► Deflocculation may hamper biomass recover during full-scale treatment. - Abstract: With the hypothesis that light supply can impact the removal of veterinary antibiotics during livestock wastewater treatment in high rate algal ponds (HRAPs), this study was undertaken to determine the mechanisms of tetracycline removal in these systems. For this purpose, two HRAPs were fed with synthetic wastewater for 46 days before tetracycline was added at 2 mg L −1 to the influent of one of the reactors (Te-HRAP). From day 62, dissolved tetracycline removal stabilized around 69 ± 1% in the Te-HRAP and evidence from batch assays suggests that this removal was mainly caused by photodegradation and biosorption. Tetracycline addition was followed by the deflocculation of the Te-HRAP biomass but had otherwise no apparent impact on the removal of the chemical oxygen demand (COD) and biomass productivity. The results from the batch assays also suggested that the light-shading and/or pollutant-sequestrating effects of the biomass limited tetracycline removal in the pond. For the first time, these results demonstrate that the shallow geometry of HRAPs is advantageous to support the photodegradation of antibiotics during wastewater biological treatment but that the presence of these pollutants could hamper biomass recovery. These findings have significant implications for algal-based environmental biotechnologies and must be confirmed under field conditions.

THE KINETICS OF NH(4)+ AND NO3(-) UPTAKE BY DOUGLAS-FIR FROM SINGLE N-SOLUTIONS AND FROM SOLUTIONS CONTAINING BOTH NH(4)+ AND NO3(-)

NARCIS (Netherlands)

KAMMINGAVANWIJK, C; PRINS, HBA

The kinetics of NH4+ and NO3- uptake in young Douglas fir trees (Pseudotsuga menziesii [Mirb.] Franco) were studied in solutions, containing either one or both N species. Using solutions containing a single N species, the V(max) of NH4+ uptake was higher than that of NO3- uptake. The K(m) of NH4+

Long-term ammonia removal in a coconut fiber-packed biofilter: analysis of N fractionation and reactor performance under steady-state and transient conditions.

Science.gov (United States)

Baquerizo, Guillermo; Maestre, Juan P; Machado, Vinicius C; Gamisans, Xavier; Gabriel, David

2009-05-01

A comprehensive study of long-term ammonia removal in a biofilter packed with coconut fiber is presented under both steady-state and transient conditions. Low and high ammonia loads were applied to the reactor by varying the inlet ammonia concentration from 90 to 260 ppm(v) and gas contact times ranging from 20 to 36 s. Gas samples and leachate measurements were periodically analyzed and used for characterizing biofilter performance in terms of removal efficiency (RE) and elimination capacity (EC). Also, N fractions in the leachate were quantified to both identify the experimental rates of nitritation and nitratation and to determine the N leachate distribution. Results showed stratification in the biofilter activity and, thus, most of the NH(3) removal was performed in the lower part of the reactor. An average EC of 0.5 kg N-NH(3)m(-3)d(-1) was obtained for the whole reactor with a maximum local average EC of 1.7 kg N-NH(3)m(-3)d(-1). Leachate analyses showed that a ratio of 1:1 of ammonium and nitrate ions in the leachate was obtained throughout steady-state operation at low ammonia loads with similar values for nitritation and nitratation rates. Low nitratation rates during high ammonia load periods occurred because large amounts of ammonium and nitrite accumulated in the packed bed, thus causing inhibition episodes on nitrite-oxidizing bacteria due to free ammonia accumulation. Mass balances showed that 50% of the ammonia fed to the reactor was oxidized to either nitrite or nitrate and the rest was recovered as ammonium indicating that sorption processes play a fundamental role in the treatment of ammonia by biofiltration.

Photocatalytic removal of nitrogen oxides from ambient air using solar energy; Taiyo energy wo riyoshita taikichu no NOx no hikari shokubai jokyo

Energy Technology Data Exchange (ETDEWEB)

Fukaya, M; Taoda, H; Watanabe, E; Nonami, T; Iseda, K; Kato, K [National Industrial Research Institute of Nagoya, Nagoya (Japan); Kunieda, S [NGK Insulators, Ltd., Nagoya (Japan); Kato, S

1997-11-25

Experiment was made on removal of NOx from ambient air using ceramic blocks coated with a newly developed easy-to- handle TiO2 film photocatalyst. After TiO2 sol was prepared by hydrolyzing titanium tetraisopropoxide, the photocatalytic blocks were prepared through drying and sintering after immersing the blocks in TiO2 sol. The effect of the number of coating on catalytic performance was studied using the single-coated and triple-coated blocks. Artificial solar light of 1mW/cm{sup 2} was used as light source for flowing reaction experiment of air (containing NOx) in a laboratory. NOx concentration rapidly decreased with irradiation, and 94% and 98% of NOx were removed by the single- and triple-coated blocks, respectively. NOx was completely oxidized to HNO3 through NO2 by triple-coated blocks. The demonstration test of removal of NOx from ambient air in Okazaki city showed a removal rate of nearly 90% in noonday and 40% or more in average, while not 0% but 5-20% even in the nighttime. The latter is probably derived from adsorption by the porous photocatalytic blocks. 2 figs., 4 tabs.

Facile one-pot construction of α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} heterojunction for arsenic removal by synchronous visible light catalysis oxidation and adsorption

Energy Technology Data Exchange (ETDEWEB)

Sun, Suwen; Ji, Chunnuan, E-mail: 1842355613@qq.com; Wu, Lingling; Chi, Shenghua; Qu, Rongjun; Li, Yan; Lu, Yangxiao; Sun, Changmei; Xue, Zhongxin

2017-06-15

α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} composites with heterojunction were prepared by facile one-pot synthesis using ferric chloride and dicyandiamide as precursors. The newly formed composites were applied to remove arsenic from aqueous solution for the first time through synchronous visible light catalysis oxidation and adsorption. α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} composites were characterized by wide-angle X-ray powder diffraction, transmission electron microscopy, high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, UV–Vis diffuse reflectance spectroscopy, and BET surface analysis. Under visible light irradiation, As(III) was oxidized to As(V) efficiently on the surface of α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4}. In addition, the oxidized arsenic could be adsorbed in situ, resulting in the effective arsenic removal. The enhancement of photocatalytic activity the composites was attributed to the construction of heterojunction between α-Fe{sub 2}O{sub 3} and g-C{sub 3}N{sub 4}. A possible oxidation mechanism of the as-composites for As(III) under visible light irradiation was also elucidated. - Highlights: • α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} composites with heterojunction was prepared by facile one-pot synthesis. • The photocatalytic activity of α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} composites under visible light irradiation for As(III) was evaluated. • Synchronous visible light catalysis oxidation and adsorption were achieved for the removal of arsenic. • The reasonable oxidation mechanism of the composites for As(III) under visible light irradiation was investigated.

Physicochemical properties influencing denitrification rate and microbial activity in denitrification bioreactors

Science.gov (United States)

Schmidt, C. A.

2012-12-01

The use of N-based fertilizer will need to increase to meet future demands, yet existing applications have been implicated as the main source of coastal eutrophication and hypoxic zones. Producing sufficient crops to feed a growing planet will require efficient production in combination with sustainable treatment solutions. The long-term success of denitrification bioreactors to effectively remove nitrate (NO¬3), indicates this technology is a feasible treatment option. Assessing and quantifying the media properties that affect NO¬3 removal rate and microbial activity can improve predictions on bioreactor performance. It was hypothesized that denitrification rates and microbial biomass would be correlated with total C, NO¬3 concentration, metrics of organic matter quality, media surface area and laboratory measures of potential denitrification rate. NO¬3 removal rates and microbial biomass were evaluated in mesocosms filled with different wood treatments and the unique influence of these predictor variables was determined using a multiple linear regression analysis. NO3 reduction rates were independent of NO¬3 concentration indicating zero order reaction kinetics. Temperature was strongly correlated with denitrification rate (r2=0.87; Q10=4.7), indicating the variability of bioreactor performance in differing climates. Fiber quality, and media surface area were strong (R>0.50), unique predictors of rates and microbial biomass, although C:N ratio and potential denitrification rate did not predict actual denitrification rate or microbial biomass. Utilizing a stepwise multiple linear regression, indicates that the denitrification rate can be effectively (r2=0.56;pdetergent fiber and surface area alone are quantified. These results will assist with the widespread implementation of denitrification bioreactors to achieve significant N load reductions in large watersheds. The nitrate reduction rate as a function of groundwater temperature for all treatments

[Effect of NH4(+) -N/NO3(-)-N ratio in applied supplementary fertilizer on nitrogen metabolism and main chemical composition of Pinellia ternata].

Science.gov (United States)

Hu, Long-Jiao; Wang, Kang-Cai; Li, Can-Wen

2013-07-01

To study the effect of nitrogen forms on nitrogen metabolism and main chemical composition of Pinellia ternate. Through the soilless cultivation experiment and based at the same nitrogen level and different NH4(+) -N/NO3(-) -N ratios, nitrate reductase (NR) activity, glutamine synthetase (GS) activity, the content of nitrate nitrogen and ammonium nitrogen in different parts of P. ternate were determined. The contents of total alkaloid, free total organic acids and guanosine in the tuber were determined. The yield of bulbil and tuber was calculated. The test results showed that, with the NH4(+) -N/NO3(-) -N ratio increasing, the activity of nitrate reductase decreased, the content of nitrate nitrogen in the leaves, petioles and tuber increasing initially, then decreased, and the content of nitrate nitrogen in the root decreased. Meanwhile, with the NH4(+) -N/NO3(-) -N ratio increasing, the activity of glutamine synthetase in the leaves, petioles and root increased, the activity of glutamine synthetase in the tuber increasing initially, then decreased. The contents of ammonium nitrogen in the leaves, tuber and root increased initially, then decreased, and the contents of ammonium nitrogen in the petioles increased with the NH4(+)(-N/NO3(-)-N ratio increasing. The yield of bulbil and tuber were the highest at the NH4(+)-N/NO3(-) -N ratio of 75: 25. The content of total alkaloid and guanosine in the tuber were the highest at the NH4(+)-N/NO3(-) -N ratio of 0: 100, and the contents were 0.245% and 0.0197% respectively. With the NH4(+)-N/NO3(-) -N ratio of 50: 50, the content of free total organic acids was the highest, it reached 0.7%, however, the content of free total organic acids was the lowest at the NH4(+) -N/NO3(-) -N ratio of 0: 100. Nitrogen fertilization significant influences the nitrogen metabolism, the yield and main chemical composition of P. ternate.

Nitrogen and Organics Removal during Riverbank Filtration along a Reclaimed Water Restored River in Beijing, China

Directory of Open Access Journals (Sweden)

Weiyan Pan

2018-04-01

Full Text Available Reclaimed water has been widely used to restore rivers and lakes in water scarce areas as well as in Beijing municipality, China. However, refilling the rivers with reclaimed water may result in groundwater pollution. A three-year field monitoring program was conducted to assess the effect of a riverbank filtration (RBF system on the removal of nitrogen and organics from the Qingyang River of Beijing, which is replenished with reclaimed water. Water samples from the river, sediment, and groundwater were collected for NO3-N, NH4-N, and chemical oxygen demand (COD was measured. The results indicate that about 85% of NO3-N was removed from the riverbed sediments. Approximate 92% of NH4-N was removed during the infiltration of water from river to aquifer. On average, 54% of COD was removed by RBF. The attenuation of NO3-N through RBF to the groundwater varied among seasons and was strongly related to water temperature. On the other hand, no obvious temporal variability was identified in the removal of COD. These results suggest that the RBF system is an effective barrier against NO3-N, NH4-N and COD in the Qingyang River, as well as those rivers with similar geological and climatic conditions refilled with reclaimed water.

Phytoremediation removal rates of benzene, toluene, and chlorobenzene.

Science.gov (United States)

Limmer, Matt A; Wilson, Jordan; Westenberg, David; Lee, Amy; Siegman, Mark; Burken, Joel G

2018-06-07

Phytoremediation is a sustainable remedial approach, although performance efficacy is rarely reported. In this study, we assessed a phytoremediation plot treating benzene, toluene, and chlorobenzene. A comparison of the calculated phytoremediation removal rate with estimates of onsite contaminant mass was used to forecast cleanup periods. The investigation demonstrated that substantial microbial degradation was occurring in the subsurface. Estimates of transpiration indicated that the trees planted were removing approximately 240,000 L of water per year. This large quantity of water removal implies substantial removal of contaminant due to large amounts of contaminants in the groundwater; however, these contaminants extensively sorb to the soil, resulting in large quantities of contaminant mass in the subsurface. The total estimate of subsurface contaminant mass was also complicated by the presence of non-aqueous phase liquids (NAPL), additional contaminant masses that were difficult to quantify. These uncertainties of initial contaminant mass at the site result in large uncertainty in the cleanup period, although mean estimates are on the order of decades. Collectively, the model indicates contaminant removal rates on the order of 10 -2 -10 0 kg/tree/year. The benefit of the phytoremediation system is relatively sustainable cleanup over the long periods necessary due to the presence of NAPL.

Vibrational spectroscopy of NO + (H2O)n: Evidence for the intracluster reaction NO + (H2O)n --> H3O + (H2O)n - 2 (HONO) at n => 4

Science.gov (United States)

Choi, Jong-Ho; Kuwata, Keith T.; Haas, Bernd-Michael; Cao, Yibin; Johnson, Matthew S.; Okumura, Mitchio

1994-05-01

Infrared spectra of mass-selected clusters NO+(H2O)n for n=1 to 5 were recorded from 2700 to 3800 cm-1 by vibrational predissociation spectroscopy. Vibrational frequencies and intensities were also calculated for n=1 and 2 at the second-order Møller-Plesset (MP2) level, to aid in the interpretation of the spectra, and at the singles and doubles coupled cluster (CCSD) level energies of n=1 isomers were computed at the MP2 geometries. The smaller clusters (n=1 to 3) were complexes of H2O ligands bound to a nitrosonium ion NO+ core. They possessed perturbed H2O stretch bands and dissociated by loss of H2O. The H2O antisymmetric stretch was absent in n=1 and gradually increased in intensity with n. In the n=4 clusters, we found evidence for the beginning of a second solvation shell as well as the onset of an intracluster reaction that formed HONO. These clusters exhibited additional weak, broad bands between 3200 and 3400 cm-1 and two new minor photodissociation channels, loss of HONO and loss of two H2O molecules. The reaction appeared to go to completion within the n=5 clusters. The primary dissociation channel was loss of HONO, and seven vibrational bands were observed. From an analysis of the spectrum, we concluded that the n=5 cluster rearranged to form H3O+(H2O)3(HONO), i.e., an adduct of the reaction products.

Nitrate removal in stream ecosystems measured by 15N addition experiments: Total uptake

Science.gov (United States)

Hall, R.O.; Tank, J.L.; Sobota, D.J.; Mulholland, P.J.; O'Brien, J. M.; Dodds, W.K.; Webster, J.R.; Valett, H.M.; Poole, G.C.; Peterson, B.J.; Meyer, J.L.; McDowell, W.H.; Johnson, S.L.; Hamilton, S.K.; Grimm, N. B.; Gregory, S.V.; Dahm, Clifford N.; Cooper, L.W.; Ashkenas, L.R.; Thomas, S.M.; Sheibley, R.W.; Potter, J.D.; Niederlehner, B.R.; Johnson, L.T.; Helton, A.M.; Crenshaw, C.M.; Burgin, A.J.; Bernot, M.J.; Beaulieu, J.J.; Arangob, C.P.

2009-01-01

We measured uptake length of 15NO-3 in 72 streams in eight regions across the United States and Puerto Rico to develop quantitative predictive models on controls of NO-3 uptake length. As part of the Lotic Intersite Nitrogen eXperiment II project, we chose nine streams in each region corresponding to natural (reference), suburban-urban, and agricultural land uses. Study streams spanned a range of human land use to maximize variation in NO-3 concentration, geomorphology, and metabolism. We tested a causal model predicting controls on NO-3 uptake length using structural equation modeling. The model included concomitant measurements of ecosystem metabolism, hydraulic parameters, and nitrogen concentration. We compared this structural equation model to multiple regression models which included additional biotic, catchment, and riparian variables. The structural equation model explained 79% of the variation in log uptake length (S Wtot). Uptake length increased with specific discharge (Q/w) and increasing NO-3 concentrations, showing a loss in removal efficiency in streams with high NO-3 concentration. Uptake lengths shortened with increasing gross primary production, suggesting autotrophic assimilation dominated NO-3 removal. The fraction of catchment area as agriculture and suburban-urban land use weakly predicted NO-3 uptake in bivariate regression, and did improve prediction in a set of multiple regression models. Adding land use to the structural equation model showed that land use indirectly affected NO-3 uptake lengths via directly increasing both gross primary production and NO-3 concentration. Gross primary production shortened SWtot, while increasing NO-3 lengthened SWtot resulting in no net effect of land use on NO- 3 removal. ?? 2009.

Re-use of winery wastewaters for biological nutrient removal.

Science.gov (United States)

Rodríguez, L; Villaseñor, J; Buendía, I M; Fernández, F J

2007-01-01

The aim of this study was to evaluate the feasibility of the re-use of the winery wastewater to enhance the biological nutrient removal (BNR) process. In batch experiments it was observed that the addition of winery wastewater mainly enhanced the nitrogen removal process because of the high denitrification potential (DNP), of about 130 mg N/g COD, of the contained substrates. This value is very similar to that obtained by using pure organic substrates such as acetate. The addition of winery wastewater did not significantly affect either phosphorus or COD removal processes. Based on the experimental results obtained, the optimum dosage to remove each mg of N-NO3 was determined, being a value of 6.7 mg COD/mg N-NO3. Because of the good properties of the winery wastewater to enhance the nitrogen removal, the viability of its continuous addition in an activated sludge pilot-scale plant for BNR was studied. Dosing the winery wastewater to the pilot plant a significant increase in the nitrogen removal was detected, from 58 to 75%. The COD removal was slightly increased, from 89 to 95%, and the phosphorus removal remained constant.

NO3 uptake in shallow, oligotrophic, mountain lakes: The influence of elevated NO3 concentrations

Science.gov (United States)

Nydick, K.R.; LaFrancois, B.M.; Baron, Jill S.

2004-01-01

Nutrient enrichment experiments were conducted in 1.2-m deep enclosures in 2 shallow, oligotrophic, mountain lakes. 15N-NO3 isotope tracer was used to compare the importance of phytoplankton and benthic compartments (epilithon, surface sediment [epipelon], and subsurface sediment) for NO3 uptake under high and low NO3 conditions. NO3 uptake approached saturation in the high-N lake, but not in the low-N lake. The capacity of phytoplankton and benthic compartments to take up NO3 differed among treatments and between lakes, and depended on water-column nutrient conditions and the history of NO3 availability. Phytoplankton productivity responded strongly to addition of limiting nutrients, and NO3 uptake was related to phytoplankton biomass and photosynthesis. However, more NO3 usually was taken up by benthic compartments (57–92% combined) than by phytoplankton, even though the response of benthic algal biomass to nutrient additions was less pronounced than that of phytoplankton and benthic NO3 uptake was unrelated to benthic algal biomass. In the low-N lake where NO3 uptake was unsaturated, C content or % was related to NO3 uptake in benthic substrates, suggesting that heterotrophic bacterial processes could be important in benthic NO3 uptake. These results suggest that phytoplankton are most sensitive to nutrient additions, but benthic processes are important for NO3 uptake in shallow, oligotrophic lakes.

[Effects of different NO3--N/NH4+-N ratios on cucumber seedlings growth, nitrogen absorption and metabolism under suboptimal temperature and light intensity].

Science.gov (United States)

Zhang, Xiao Cui; Liu, Yu Mei; Bai, Long Qiang; He, Chao Xing; Yu, Xian Chang; Li, Yan Su

2016-08-01

Cucumber (cv. Zhongnong 26) was used as material, the effects of NO 3 - -N/NH 4 + -N ratios on growth and physiological characteristics of cucumber seedlings under suboptimal temperature and light intensity (18 ℃/10 ℃,180 ± 20 μmol·m -2 ·s -1 ) were studied. Total nitrogen in the nutrient solution was equal and three NO 3 - -N/NH 4 + -N ratios, 26:2, 21:7 and 14:14, were applied as treatments. The results showed that cucumber treated by NO 3 - -N/NH 4 + -N=21:7 had the longest total root length, the biggest root volume and root surface area, and the maximum number of root tips. H + -ATPase activity and relative expression of genes encoding nitrate transporter (NRT) and ammonium transporter (AMT) in cucumber roots were increased significantly by the treatment of NO 3 - -N/NH 4 + -N=21:7. In addition, nitrate reductase (NR), glutamine synthetase (GS) and glutamate synthase (GOGAT) in cucumber leaves under the treatment of NO 3 - -N/NH 4 + -N=21:7 were higher. As a result, the nitrogen content and biomass of cucumber were significantly increased. Compared with the plants under the treatment of NO 3 - -N/NH 4 + -N=26:2 or 14:14, cucumber seedlings under the treatment of NO 3 - -N/NH 4 + -N=21:7 had the highest biomass and total dry mass (DM) which were increased by 14.0% and 19.3% respectively under suboptimal temperature and light intensity. In conclusion, under suboptimal environmental conditions, NO 3 - -N/NH 4 + -N ratio could be adjusted to increase nitrogen absorption and metabolism of cucumber and alleviate the de-trimental effects caused by suboptimal conditions and promoted the cucumber growth.

Enhanced nitrogen removal in single-chamber microbial fuel cells with increased gas diffusion areas

KAUST Repository

Yan, Hengjing

2012-11-23

Single-chamber microbial fuel cells (MFCs) with nitrifiers pre-enriched at the air cathodes have previously been demonstrated as a passive strategy for integrating nitrogen removal into current-generating bioelectrochemical systems. To further define system design parameters for this strategy, we investigated in this study the effects of oxygen diffusion area and COD/N ratio in continuous-flow reactors. Doubling the gas diffusion area by adding an additional air cathode or a diffusion cloth significantly increased the ammonia and COD removal rates (by up to 115% and 39%), ammonia removal efficiency (by up to 134%), the cell voltage and cathode potentials, and the power densities (by a factor of approximately 2). When the COD/N ratio was lowered from 13 to 3, we found up to 244% higher ammonia removal rate but at least 19% lower ammonia removal efficiency. An increase of COD removal rate by up to 27% was also found when the COD/N ratio was lowered from 11 to 3. The Coulombic efficiency was not affected by the additional air cathode, but decreased by an average of 11% with the addition of a diffusion cloth. Ammonia removal by assimilation was also estimated to understand the ammonia removal mechanism in these systems. These results showed that the doubling of gas diffusion area enhanced N and COD removal rates without compromising electrochemical performance. © 2012 Wiley Periodicals, Inc.

La3+-modified activated alumina for fluoride removal from water

International Nuclear Information System (INIS)

Cheng, Jiemin; Meng, Xiaoguang; Jing, Chuanyong; Hao, Jumin

2014-01-01

Graphical abstract: - Highlights: • A La 3+ -modified activated alumina adsorbent was prepared for effective removal F − . • SEM/EDS and EXAFS analyses determined the formation of La(OH) 3 coating on the AA. • The La-AA had much high adsorption rate and capacity than the AA. • The La-AA was promising adsorbent for effective removal of F − from water. - Abstract: A La 3+ -modified activated alumina (La-AA) adsorbent was prepared for effective removal of fluoride from water. The surface properties of adsorbent were characterized with zeta potential analysis, SEM-EDS and EXAFS. Batch and column experiments were conducted to evaluate improvement of F − removal by the La-AA. SEM/EDS and EXAFS analyses determined the formation of La(OH) 3 coating on the AA and strong bonding interactions between La 3+ and the Al atoms. The points of zero charge (pH PZC ) of AA and La-AA were at pH 8.94 and 9.57, respectively. Batch experimental results indicated that the La-AA had much higher adsorption rate and capacity than the AA. The F − adsorption processes on La-AA and AA followed the pseudo-second-order kinetics and the Langmuir isotherm. Column filtration results shows that the La-AA and AA treated 270 and 170 bed volumes of the F − -spiked tap water, respectively, before F − breakthrough occurred. The results demonstrated that the La-AA was a promising adsorbent for effective removal of F − from water

{2-[(3,5-Dichloro-2-oxidobenzylideneamino-κ2N,O]-3-methylpentanoato-κO}(N,N′-dimethylformamide-κOcopper(II

Directory of Open Access Journals (Sweden)

Xiao Zhen Feng

2008-05-01

Full Text Available In the title compound, [Cu(C13H13Cl2NO3(C3H7NO], the CuII atom is coordinated in a slightly distorted square-planar geometry by two O atoms and one N atom from the tridentate chiral ligand 2-[(3,5-dichloro-2-oxidobenzylideneamino]-3-methylpentanoate and by one O atom from dimethylformamide. In the crystal structure, the Cu atom forms contacts with Cl and O atoms of two units (Cu...Cl and Cu...O = 3.401 and 2.947 Å, respectively, thereby forming an approximately octahedral arrangement. A three-dimensional network is constructed through Cl...Cu, O...Cu, Cl...Cl contacts and C—H...O hydrogen bonds.

Effect of powdered activated carbon technology on short-cut nitrogen removal for coal gasification wastewater.

Science.gov (United States)

Zhao, Qian; Han, Hongjun; Xu, Chunyan; Zhuang, Haifeng; Fang, Fang; Zhang, Linghan

2013-08-01

A combined process consisting of a powdered activated carbon technology (PACT) and short-cut biological nitrogen removal reactor (SBNR) was developed to enhance the removal efficiency of the total nitrogen (TN) from the effluent of an upflow anaerobic sludge bed (UASB) reactor, which was used to treat coal gasification wastewater (CGW). The SBNR performance was improved with the increasing of COD and TP removal efficiency via PACT. The average removal efficiencies of COD and TP in PACT were respectively 85.80% and 90.30%. Meanwhile, the NH3-N to NO2-N conversion rate was achieved 86.89% in SBNR and the total nitrogen (TN) removal efficiency was 75.54%. In contrast, the AOB in SBNR was significantly inhibited without PACT or with poor performance of PACT in advance, which rendered the removal of TN. Furthermore, PAC was demonstrated to remove some refractory compounds, which therefore improved the biodegradability of the coal gasification wastewater. Copyright © 2013 The Authors. Published by Elsevier Ltd.. All rights reserved.

Post-Removal Examination of GTF Cathode No.2

International Nuclear Information System (INIS)

Kirby, R.

2005-01-01

This photo-cathode (PC), GTF Cathode No.2, was removed from the GTF in October, 2000. It was characterized in September, 1999 by G. Mulhollan and me (Report entitled ''A Brief Report on a Brief Examination of the Electropolished GTF Cathode'', LCLS-TN-99-10). The cathode conditions and results of that exam were: (1) The cathode was conventionally machined and cleaned in the SLAC Plating Shop. (2) The machining process left a central defect (400 microns diameter) which was not removed by electropolishing. (3) The electropolished surface was ''orange-peeled'', typical of excessive polishing. (4) Secondary electron microscopy (SEM) examination showed numerous 10 micron-diameter etch pits and a small number of copper surface particles. Operation of this cathode in the GTF exhibited ''holloW--beam'' behavior, suggesting that the central defect may have been responsible for non-normal emergence of the photo-emitted beam. No laser cleaning of the cathode was done, so all arc features are due to breakdowns. Post-removal analysis consisted of loW--magnification digital camera pictures (taken with glancing-incidence tungsten white light illumination, to emphasize particles/pitting) and SEM. All images are available in digital (TIFF) form. Also available is a Power Point presentation of the results. Contact me for either. These image files are high-resolution and, thus, large in size. A 200K loW--resolution contact sheet of a few images is attached to this report. Images are referred to by file name

An Advanced Semimetal-Organic Bi Spheres-g-C3N4 Nanohybrid with SPR-Enhanced Visible-Light Photocatalytic Performance for NO Purification.

Science.gov (United States)

Dong, Fan; Zhao, Zaiwang; Sun, Yanjuan; Zhang, Yuxin; Yan, Shuai; Wu, Zhongbiao

2015-10-20

To achieve efficient photocatalytic air purification, we constructed an advanced semimetal-organic Bi spheres-g-C3N4 nanohybrid through the in-situ growth of Bi nanospheres on g-C3N4 nanosheets. This Bi-g-C3N4 compound exhibited an exceptionally high and stable visible-light photocatalytic performance for NO removal due to the surface plasmon resonance (SPR) endowed by Bi metal. The SPR property of Bi could conspicuously enhance the visible-light harvesting and the charge separation. The electromagnetic field distribution of Bi spheres involving SPR effect was simulated and reaches its maximum in close proximity to the Bi particle surface. When the Bi metal content was controlled at 25%, the corresponding Bi-g-C3N4 displayed outstanding photocatalytic capability and transcended those of other visible-light photocatalysts. The Bi-g-C3N4 exhibited a high structural stability under repeated photocatalytic runs. A new visible-light-induced SPR-based photocatalysis mechanism with Bi-g-C3N4 was proposed on the basis of the DMPO-ESR spin-trapping. The photoinduced electrons could transfer from g-C3N4 to the Bi metal, as revealed with time-resolved fluorescence spectra. The function of Bi semimetal as a plasmonic cocatalyst for boosting visible light photocatalysis was similar to that of noble metals, which demonstrated a great potential of utilizing the economically feasible Bi element as a substitute for noble metals for the advancement of photocatalysis efficiency.

Nitrogen removal from concentrated latex wastewater by land treatment

Directory of Open Access Journals (Sweden)

Vikanda Thongnuekhang

2004-05-01

Full Text Available Most of the concentrated latex factories in the South of Thailand discharge treated wastewater that contains high level of nitrogen to a nearby river or canals leading to a water pollution problem. A study of land treatment system was conducted to treat and utilize nitrogen in treated wastewater from the concentrated latex factory. The experimental pilot-scale land treatment system was constructed at the Faculty of Engineering, Prince of Songkla University, Hat Yai Campus. It consisted of water convolvulus (Ipomea aquatica, I. Reptans, tropical carpet grass (Axonopus compresus (Swartz Beav. and control unit (no plantation. The treated wastewater from the stabilization pond system of the selected concentrated latex factoryin Songkhla was used to irrigate each experimental unit. Influent and effluent from the experimental units were analyzed for TKN, NH3-N, Org-N, NO3 --N, NO2 --N, BOD5, sulfate, pH and EC. The land treatment system resulted a high removal efficiency for nitrogen. Tropical carpet grass provided higher removal efficiency than other units for all parameters. The removal efficiency of water convolvulus and control unit were not significantly different. The average removal efficiency of TKN, NH3-N, Org-N, BOD5 and sulfate for tropical carpet grass unit were 92, 97, 61, 88 and 52%, for water convolvulus unit were 75, 80, 43, 41 and 30%, and for control unit were 74, 80, 41, 31 and 28%, respectively. Mass balance of nitrogen transformation was conducted. It revealed that plant uptake was the major mechanism for nitrogen removal in land treatment.

Kinetic Interpretation of Nitrogen Removal in Pilot Scale Experiments

DEFF Research Database (Denmark)

Harremoës, Poul; Sinkjær, Ole

1995-01-01

with biological and chemical phosphorus removal. Nitrification and denitrification rates have been measured in batch tests on activated sludge extracted from the pilot plants and by measuring transient concentrations during the alternating mode of operation in the aerobic and anoxic tanks. The data were......Pilot plant experiments have been performed over a period of four years in order to establish an experimental basis for the upgrading of the treatment plants of The City of Copenhagen to nutrient removal. The choice of design is the alternating mode of operating biological nitrogen removal...... normalized to standard conditions by correcting them according to the kinetic theory. The average normalized nitrification rate was measured to be between 54 and 60 mg NH~-N/(g VSSn~t' h) by different test methods at 7°C. The denitrification rate was measured to vary between 0.85 and 0.95mg NO~--N/(g VSS. h...

Nitrogen fertilization (15NH4NO3 of palisadegrass and residual effect on subsequent no-tillage corn

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Emerson Borghi

2014-10-01

Full Text Available Nitrogen is required in large amounts by plants and their dinamics in corn and perennial forages intercropped is little known. This study analyzed the efficiency of nitrogen fertilization (15NH4NO3 applied after corn grain harvest to palisadegrass (Brachiaria brizantha cv. Marandu in intercrops sown at two times, as well as the N residual effect on the subsequent corn crop. The field experiment was performed in Botucatu, São Paulo State, in southeastern Brazil, on a structured Alfisol under no-tillage. The experiment was arranged in a randomized block design in a split plot scheme with four replications. The main plots consisted of two intercropping systems (corn and palisadegrass sown together and palisadegrass sown later, at corn top-dressing fertilization. The subplots consisted of four N rates (0, 30, 60, and 120 kg ha-1 N. The subplots contained microplots, in which enriched ammonium nitrate (15NH4NO3 was applied at the same rates. The time of intercrop sowing affected forage dry matter production, the amount of fertilizer-derived N in and the N use efficiency by the forage plants. Nitrogen applied in autumn to palisadegrass intercropped with corn, planted either at corn sowing or at N top-dressing fertilization, increased the forage yield up to a rate of 60 kg ha-1. The amount of fertilizer-derived N by the forage plants and the fertilizer use efficiency by palisadegrass were highest 160 days after fertilization for both intercrop sowing times, regardless of N rates. Residual N did not affect the N nutrition of corn plants grown in succession to palisadegrass, but increased grain yield at rates of 60 and 120 kg ha-1 N, when corn was grown on palisadegrass straw from the intercrop installed at corn fertilization (top-dressing. Our results indicated that the earlier intercropping allowed higher forage dry matter production. On the other hand, the later intercrop allowed a higher corn grain yield in succession to N-fertilized palisadegrass.

Sodium isotopic exchange rate between crystalline zirconium phosphate and molten NaNO/sub 3/

Energy Technology Data Exchange (ETDEWEB)

Inoue, Y; Yamada, Y [Tohoku Univ., Sendai (Japan). Faculty of Engineering

1975-12-01

The isotopic exchange rate of sodium ion between crystalline zirconium phosphate and molten NaNO/sub 3/ has been measured at 312/sup 0/C and 362/sup 0/C by batch method. The equilibrium was reached within 20 minutes at either temperature, and the rate was very rapid as compared with that of sodium-potassium ion exchange.

epsilon-N-trimethyllysine availability regulates the rate of carnitine biosynthesis in the growing rat

International Nuclear Information System (INIS)

Rebouche, C.J.; Lehman, L.J.; Olson, L.

1986-01-01

Rates of carnitine biosynthesis in mammals depend on the availability of substrates and the activity of enzymes subserving the pathway. This study was undertaken to test the hypothesis that the availability of epsilon-N-trimethyllysine is rate-limiting for synthesis of carnitine in the growing rat and to evaluate diet as a source of this precursor for carnitine biosynthesis. Rats apparently absorbed greater than 90% of a tracer dose of [methyl- 3 H]epsilon-N-trimethyllysine, and approximately 30% of that was incorporated into tissues as [ 3 H]carnitine. Rats given oral supplements of epsilon-N-trimethyllysine (0.5-20 mg/d), but no dietary carnitine, excreted more carnitine than control animals receiving no dietary epsilon-N-trimethyllysine or carnitine. Rates of carnitine excretion increased in a dose-dependent manner. Tissue and serum levels of carnitine also increased with dietary epsilon-N-trimethyllysine supplementation. There was no evidence that the capacity for carnitine biosynthesis was saturated even at the highest level of oral epsilon-N-trimethyllysine supplementation. Common dietary proteins (casein, soy protein and wheat gluten) were found to be poor sources of epsilon-N-trimethyllysine for carnitine biosynthesis. The results of this study indicate that the availability of epsilon-N-trimethyllysine limits the rate of carnitine biosynthesis in the growing rat

Novel MBR_based main stream biological nutrient removal process: high performance and microbial community.

Science.gov (United States)

Zhang, Chuanyi; Xu, Xinhai; Zhao, Kuixia; Tang, Lianggang; Zou, Siqi; Yuan, Limei

2018-02-01

For municipal wastewater treatment, main stream biological nutrient removal (BNR) process is becoming more and more important. This lab-scale study, novel MBR_based BNR processes (named A 2 N-MBR and A 2 NO-MBR) were built. Comparison of the COD removal, results obtained demonstrated that COD removal efficiencies were almost the same in three processes, with effluent concentration all bellowed 30 mg L -1 . However, the two-sludge systems (A 2 N-MBR and A 2 NO-MBR) had an obvious advantage over the A 2 /O for denitrification and phosphorus removal, with the average TP removal rates of 91.20, 98.05% and TN removal rates of 73.00, 79.49%, respectively, higher than that of 86.45 and 61.60% in A 2 /O process. Illumina Miseq sequencing revealed that Candidatus_Accumulibacter, which is capable of using nitrate as an electron acceptor for phosphorus and nitrogen removal simultaneously, was the dominant phylum in both A 2 N-MBR and A 2 NO-MBR process, accounting for 28.74 and 23.98%, respectively. Distinguishingly, major organism groups related to nitrogen and phosphorus removal in A 2 /O system were Anaerolineaceae_uncultured, Saprospiraceae_uncultured and Thauera, with proportions of 11.31, 8.56 and 5.00%, respectively. Hence, the diversity of dominant PAOs group was likely responsible for the difference in nitrogen and phosphorus removal in the three processes.

High-Pressure Synthesis and Study of NO+NO3− and NO2+NO3− Ionic Solids

Directory of Open Access Journals (Sweden)

A. Yu. Kuznetsov

2009-01-01

Full Text Available Nitrosonium-nitrate NO+NO3− and dinitrogen pentoxide NO2+NO3− ionic crystals were synthesized by laser heating of a condensed oxygen-rich O2-N2 mixture compressed to different pressures, up to 40 GPa, in a diamond anvil cell (DAC. High-pressure/high-temperature Raman and X-ray diffraction studies of synthesized samples disclosed a transformation of NO+NO3− compound to NO2+NO3− crystal at temperatures above ambient and pressures below 9 GPa. High-pressure experiments revealed previously unreported bands in Raman spectra of NO+NO3− and NO2+NO3− ionic crystals. Structural properties of both ionic compounds are analyzed. Obtained experimental results support a hypothesis of a rotational disorder of NO+ complexes in NO+NO3− and indicate a rotational disorder of ionic complexes in NO2+NO3− solid.

Pulse radiolysis study of NaNO/sub 2/ and NaNO/sub 3/ solutions. [Electrons

Energy Technology Data Exchange (ETDEWEB)

Broszkiewicz, R K [Institute of Nuclear Research, Warsaw (Poland)

1976-01-01

The pulse radiolysis of aqueous solutions of NaNO/sub 2/ and NaNO/sub 3/ has been done. In the nitrate solutions the transient species NO/sup 2 -//sub 2/ and NO/sub 2/ have been observed, the former reacting with water to produce NO, the latter dimerizing to N/sub 2/O/sub 4/. In the presence of O/sub 2/ and unidentified species with absorption maximum at 280 nm, probably a peroxy compound, is being formed. The radiolytic processes occurring in the nitrite solution do not depend on /NO/sub 02// and no effect of the direct energy absorption by NO/sup -//sub 2/ has been noticed. Transient species in the diluted nitrate solution are NO/sup 2 -//sub 3/ and the pernitrous ion; in concentrated solutions NO/sub 3/ is the main transient product. NO/sub 3/ is formed by the direct energy absorption by NO/sup -//sub 3/. Participation in tha effect of the cation should not be disregarded. There is evidence that the 340 nm peak in the transient spectrum is probably connected with N/sub 2/O/sub 4/ and not with NO/sub 3/. The tranient spectra, extinction coefficients of products and rate constants of relevant reactions are given.

N-Basin water removal plan

International Nuclear Information System (INIS)

Nellesen, A.L.

1997-07-01

This ALARA review provides a description of the engineering and administrative controls used to manage personnel exposure, control contamination levels, and airborne radioactivity concentrations, while removing water and stabilizing surfaces in the 105-N Fuel Storage Building

Autotrophic nitrogen removal process in a potable water treatment biofilter that simultaneously removes Mn and NH4(+)-N.

Science.gov (United States)

Cai, Yan'an; Li, Dong; Liang, Yuhai; Zeng, Huiping; Zhang, Jie

2014-11-01

Ammonia (NH4(+)-N) removal pathways were investigated in a potable water treatment biofilter that simultaneously removes manganese (Mn) and NH4(+)-N. The results indicated a significant loss of nitrogen in the biofilter. Both the completely autotrophic nitrogen removal over nitrite (CANON) process and nitrification were more likely to contribute to NH4(+)-N removal. Moreover, the model calculation results demonstrated that the CANON process contributed significantly to the removal of NH4(+)-N. For influent NH4(+)-N levels of 1.030 and 1.749mg/L, the CANON process contribution was about 48.5% and 46.6%, respectively. The most important finding was that anaerobic ammonia oxidation (ANAMMOX) bacteria were detectable in the biofilter. It is interesting that the CANON process was effective even for such low NH4(+)-N concentrations. Copyright © 2014 Elsevier Ltd. All rights reserved.

A new cavity ring-down instrument for airborne monitoring of N2O5, NO3, NO2 and O3 in the upper troposphere lower stratosphere

Science.gov (United States)

Ruth, Albert A.; Brown, Steven S.; Dinesan, Hemanth; Dubé, William P.; Goulette, Marc; Hübler, Gerhard; Orphal, Johannes; Zahn, Andreas

2016-04-01

The chemistry of NO3 and N2O5 is important to the regulation of both tropospheric and stratospheric ozone. In situ detection of NO3 and N2O5 in the upper troposphere lower stratosphere (UTLS) represents a new scientific direction as the only previous measurements of these species in this region of the atmosphere has been via remote sensing techniques. Because both the sources and the sinks for NO3 and N2O5 are potentially stratified spatially, their mixing ratios, and their influence on nitrogen oxide and ozone transport and loss at night can show large variability as a function of altitude. Aircraft-based measurements of heterogeneous N2O5 uptake in the lower troposphere have uncovered a surprising degree of variability in the uptake coefficient [1], but there are no corresponding high altitude measurements.The UTLS is routinely sampled by the IAGOS-CARIBIC program (Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrument Container, www.caribic-atmospheric.com), a European infrastructural program with the aim of studying the chemistry and transport across this part of the atmosphere. An airfreight container with 15 different automated instruments from 8 European research partners is utilized on board a commercial Lufthansa airbus 340-600 to monitor ~ 100 atmospheric species (trace gases and aerosol parameters) in the UTLS. The instrumentation in the CARIBIC container is now to be supplemented by a new cavity ring-down device for monitoring nitrogen oxides, jointly developed by researchers from Cork (Ireland), Boulder (USA) and Karlsruhe (Germany). The compact and light-weight instrument is designed to monitor not only NO3 and N2O5, but also NO2 and O3. The detection is based on 4 high-finesse optical cavities (cavity length ~ 44 cm). Two cavities are operated at 662 nm (maximum absorption of NO3), the other two at 405 nm (maximum absorption of NO2). The inlet to one of the (662)-cavities is heated in order to thermally decompose N2O5

Porous Ni3(NO3)2(OH)4 nano-sheets for supercapacitors: Facile synthesis and excellent rate performance at high mass loadings

Science.gov (United States)

Shi, Mingjie; Cui, Mangwei; Kang, Litao; Li, Taotao; Yun, Shan; Du, Jing; Xu, Shoudong; Liu, Ying

2018-01-01

For supercapacitors, pores in electrode materials can accelerate chemical reaction kinetics by shortening ion diffusion distances and by enlarging electrolyte/electrode interfaces. This article describes a simple one-step route for the preparation of pure-phase porous Ni3(NO3)2(OH)4 nano-sheets by directly heating a mild Ni(NO3)2 and urea solution. During heating, urea decomposed into NH3·H2O, which provided a suitable alkaline environment for the formation of Ni3(NO3)2(OH)4 nano-sheets. Meanwhile, the side product, NH4NO3, created numerous pores as a pore-forming agent. After NH4NO3 removal, the specific surface areas and pore volumes of products were boosted by ∼180-times (from 0.61 to 113.12 m2/g) and ∼90-times (from 3.40 × 10-3 to 3.17 × 10-1 m2/g), respectively. As a cathode material of supercapacitor, the porous Ni3(NO3)2(OH)4 nano-sheets exhibited a high specific capacitance of 1094 F/g at an ultrahigh mass loading of 17.55 mg/cm2, leading to an impressive areal capacitance of 19.2 F/cm2. Furthermore, a Ni3(NO3)2(OH)4 nano-sheet//commercial active carbon asymmetric supercapacitor was constructed and delivered an energy density of 33.2 Wh/Kg at a power density of 190.5 W/Kg, based on the mass of active materials on both electrodes.

Kinetics and mechanism of diclofenac removal using ferrate(VI): roles of Fe3+, Fe2+, and Mn2.

Science.gov (United States)

Zhao, Junfeng; Wang, Qun; Fu, Yongsheng; Peng, Bo; Zhou, Gaofeng

2018-06-01

In this study, the effect of Fe 3+ , Fe 2+ , and Mn 2+ dose, solution pH, reaction temperature, background water matrix (i.e., inorganic anions, cations, and natural organic matters (NOM)), and the kinetics and mechanism for the reaction system of Fe(VI)/Fe 3+ , Fe(VI)/Fe 2+ , and Fe(VI)/Mn 2+ were investigated systematically. Traces of Fe 3+ , Fe 2+ , and Mn 2+ promoted the DCF removal by Fe(VI) significantly. The pseudo-first-order rate constant (k obs ) of DCF increased with decreasing pH (9-6) and increasing temperature (10-30 °C) due to the gradually reduced stability and enhanced reactivity of Fe(VI). Cu 2+ and Zn 2+ ions evidently improved the DCF removal, while CO 3 2- restrained it. Besides, SO 4 2- , Cl - , NO 3 - , Mg 2+ , and Ca 2+ almost had no influence on the degradation of DCF by Fe(VI)/Fe 3+ , Fe(VI)/Fe 2+ , and Fe(VI)/Mn 2+ within the tested concentration. The addition of 5 or 20 mg L -1 NOM decreased the removal efficiency of DCF. Moreover, Fe 2 O 3 and Fe(OH) 3 , the by-products of Fe(VI), slightly inhibited the DCF removal, while α-FeOOH, another by-product of Fe(VI), showed no influence at pH 7. In addition, MnO 2 and MnO 4 - , the by-products of Mn 2+ , enhanced the DCF degradation due to catalysis and superposition of oxidation capacity, respectively. This study indicates that Fe 3+ and Fe 2+ promoted the DCF removal mainly via the self-catalysis for Fe(VI), and meanwhile, the catalysis of Mn 2+ and the effect of its by-products (i.e., MnO 2 and MnO 4 - ) contributed synchronously for DCF degradation. Graphical abstract ᅟ.

The role of C:N:P stoichiometry in affecting denitrification in sediments from agricultural surface and tile-water wetlands.

Science.gov (United States)

Grebliunas, Brian D; Perry, William L

2016-01-01

Nutrient stoichiometry within a wetland is affected by the surrounding land use, and may play a significant role in the removal of nitrate (NO3-N). Tile-drained, agricultural watersheds experience high seasonal inputs of NO3-N, but low phosphorus (PO4-P) and dissolved organic carbon (DOC) loads relative to surface water dominated systems. This difference may present stoichiometric conditions that limit denitrification within receiving waterways. We investigated how C:N:P ratios affected denitrification rates of sediments from tile-drained mitigation wetlands incubated for: 0, 5, 10, and 20 days. We then tested whether denitrification rates of sediments from surface-water and tile-drained wetlands responded differently to C:N ratios of 2:1 versus 4:1. Ratios of C:N:P (P tile-drained wetland sediments. Carbon limitation of denitrification became evident at elevated NO3-N concentrations (20 mg L(-1)). Denitrification measured from tile water and surface water wetland sediments increased significantly (P < 0.05) at the 2:1 and 4:1 C:N treatments. The results from both experiments suggest wetland sediments provide a limiting pool of labile DOC to maintain prolonged NO3-N removal. Also, DOC limitation became more evident at elevated NO3-N concentrations (20 mg L(-1)). Irrespective of NO3-N concentrations, P did not limit denitrification rates. In addition to wetting period, residence time, and maintenance of anaerobic conditions, the availability of labile DOC is playing an important limiting role in sediment denitrification within mitigation wetlands.

Evaporation Rate Study and NDMA Formation from UDMH/NO2 Reaction Products

Science.gov (United States)

Buchanan, Vanessa D.; Dee, Louis A.; Baker, David L.

2003-01-01

Laboratory samples of uns-dimethylhydrazine (UDMH) fuel/oxidizer (nitrogen dioxide) non-combustion reaction products (UFORP) were prepared using a unique permeation tube technology. Also, a synthetic UFORP was prepared from UDMH, N-nitrosodimethylamine (NDMA), dimethylammonium nitrate, sodium nitrite and purified water. The evaporation rate of UFORP and synthetic UFORP was determined under space vacuum (approx 10(exp -3) Torr) at -40 ?C and 0 ?C. The material remaining was analyzed and showed that the UFORP weight and NDMA concentration decreased over time; however, NDMA had not completely evaporated. Over 85% of the weight was removed by subjecting the UFORP to 10(-3) Torr for 7 hours at -40 ?C and 4 hours at 0 ?C. A mixture of dimethylammonium nitrate and sodium nitrite formed NDMA at a rapid rate in a moist air environment. A sample of UFORP residue was analyzed for formation of NDMA under various conditions. It was found that NDMA was not formed unless nitrite was added.

Effects of different external carbon sources and electron acceptors on interactions between denitrification and phosphorus removal in biological nutrient removal processes.

Science.gov (United States)

Hu, Xiang; Sobotka, Dominika; Czerwionka, Krzysztof; Zhou, Qi; Xie, Li; Makinia, Jacek

The effects of two different external carbon sources (acetate and ethanol) and electron acceptors (dissolved oxygen, nitrate, and nitrite) were investigated under aerobic and anoxic conditions with non-acclimated process biomass from a full-scale biological nutrient removal-activated sludge system. When acetate was added as an external carbon source, phosphate release was observed even in the presence of electron acceptors. The release rates were 1.7, 7.8, and 3.5 mg P/(g MLVSS·h) (MLVSS: mixed liquor volatile suspended solids), respectively, for dissolved oxygen, nitrate, and nitrite. In the case of ethanol, no phosphate release was observed in the presence of electron acceptors. Results of the experiments with nitrite showed that approximately 25 mg NO 2 -N/L of nitrite inhibited anoxic phosphorus uptake regardless of the concentration of the tested external carbon sources. Furthermore, higher denitrification rates were obtained with acetate (1.4 and 0.8 mg N/(g MLVSS·h)) compared to ethanol (1.1 and 0.7 mg N/ (g MLVSS·h)) for both anoxic electron acceptors (nitrate and nitrite).

Effects of C/N ratio on nitrate removal and floc morphology of autohydrogenotrophic bacteria in a nitrate-containing wastewater treatment process.

Science.gov (United States)

Nguyen, Tran Ngoc Phu; Chao, Shu-Ju; Chen, Pei-Chung; Huang, Chihpin

2018-07-01

The effects of C/N ratio of a nitrate-containing wastewater on nitrate removal performed by autohydrogenotrophic bacteria as well as on the morphological parameters of floc such as floc morphology, floc number distribution, mean particle size (MPS), aspect ratio and transparency were examined in this study. The results showed that the nitrate reduction rate increased with increasing C/N ratio from 0.5 to 10 and that the nitrogen removal of up to 95% was found at the C/N ratios of higher than 5 (between 0.5-10). Besides, high C/N ratio values reflected a corresponding high nitrite accumulation after 12-hr operation, and a fast decreasing rate of nitrite in the rest of operational time. The final pH values increased with the C/N ratio increasing from 0.5 to 2.5, but decreased with the C/N ratio increasing from 2.5 to 10. There were no significant changes in floc morphology with the MPSs ranging from 35 to 40μm. Small and medium-sized flocs were dominant in the sludge suspension, and the number of flocs increased with the increasing C/N ratios. Furthermore, the highest apparent frequency of 10% was observed at aspect ratios of 0.5 and 0.6, while the transparency of flocs changed from 0.1 to 0.7. Copyright © 2017. Published by Elsevier B.V.

Effect of rutile TiO{sub 2} on the photocatalytic performance of g-C{sub 3}N{sub 4}/brookite-TiO{sub 2-x}N{sub y} photocatalyst for NO decomposition

Energy Technology Data Exchange (ETDEWEB)

Li, Huihui, E-mail: lihh@lzu.edu.cn [Key Laboratory for Magnetism Magnetic Materials of the Ministry of Education, Lanzhou University, 222 south Tianshui Road, Lanzhou, 730000 (China); Wu, Xiaoyong [Wuhan University of Technology, 122 Luoshi Road, Wuhan 430070 (China); Yin, Shu [Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Katsumata, Kenichi [Photocatalysis International Research Center, Research Institute for Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba, 278-8510 (Japan); Wang, Yuhua [Key Laboratory for Magnetism Magnetic Materials of the Ministry of Education, Lanzhou University, 222 south Tianshui Road, Lanzhou, 730000 (China)

2017-01-15

Graphical abstract: g-C{sub 3}N{sub 4}/rutile-brookite TiO{sub 2-x}Ny forms a Z-scheme photocatalytic system, which shows improvement on the photocatalytic activity than that of g-C{sub 3}N{sub 4}/single brookite TiO{sub 2-x}N{sub y}. - Highlights: • g-C{sub 3}N{sub 4}/rutile-brookite TiO{sub 2-x}N{sub y} forms a Z-scheme photocatalytic system. • Photogenerated electrons can efficiently transfer from rutile TiO{sub 2} to g-C{sub 3}N{sub 4}. • Single brookite TiO{sub 2-x}N{sub y} shows lower photo-utilization efficiency than rutile-brookite mixed one. • DeNO{sub x} activities of brookite TiO{sub 2-x}N{sub y} hybrids decrease with g-C{sub 3}N{sub 4} amount increase. - Abstract: Novel g-C{sub 3}N{sub 4}/rutile-brookite TiO{sub 2-x}N{sub y} composite photocatalysts were fabricated through a facile solvothermal approach. The effect of rutile phase TiO{sub 2} with brookite TiO{sub 2} and g-C{sub 3}N{sub 4} on the photocatalytic activity of g-C{sub 3}N{sub 4}/nitrogen-doped TiO{sub 2} composite was studied. The photocatalytic performance of the photocatalyst was evaluated by measuring the degradation of NO gas under visible and UV light irradiation. It is suggested that g-C{sub 3}N{sub 4}/rutile-brookite TiO{sub 2-x}N{sub y} forms a Z-scheme photocatalytic system, which shows improvement on the photocatalytic activity than that of g-C{sub 3}N{sub 4}/single brookite TiO{sub 2-x}N{sub y}. By importing rutile phase TiO{sub 2-x}N{sub y}, the photogenerated electrons can efficiently transfer from rutile TiO{sub 2} to g-C{sub 3}N{sub 4}, which results in the separation of electron and hole pairs, enhancing the photocatalytic ability. However, single brookite TiO{sub 2-x}N{sub y} can not remove the photogenerated electrons efficiently and the photocatalytic performances of composites decrease with g-C{sub 3}N{sub 4} amount increase.

The electronic quenching rates of NO(A2Σ+, v'=0-2)

International Nuclear Information System (INIS)

Nee, J.B.; Juan, C.Y.; Hsu, J.Y.; Yang, J.C.; Chen, W.J.

2004-01-01

The electronic quenching rates of NO(A 2 Σ + , v ' =0-2) are measured for the gases He, Ar, Xe, N 2 , O 2 , CO 2 , N 2 O, and SF 6 . The variations of the fluorescence intensity were measured for the (0,0), (1,0), and (2,0) bands of the γ band system when the quencher gases were added. The quenching rates were determined by using the Stern-Volmer plots with the known radiative lifetimes of the excited states. The electronic quenching rate constants are fast for the group of gases of O 2 , CO 2 , N 2 O, and SF 6 , whose quenching rate constants are in the order of 10 -10 cm 3 /s. The quenching rate constants are slow for the group of gases including He, Ar, Xe, and N 2 whose rate constants are in the order of 10 -14 cm 3 /s. For the slow group, the quenching rate constants increase rapidly for v ' =2 compared with those of v ' =0 and 1. The charge transfer model and collision complex model are used to understand the quenching mechanism. For the fast group which mainly consists of gases with positive electron affinities, the charge transfer model adequately describes the mechanism. For the slow quenching group, a theoretical background is provided by consider the coupling of initial and final states in the complex potential surfaces

Probabilistic Determination of Green Infrastructure Pollutant Removal Rates from the International Stormwater BMP Database

Science.gov (United States)

Gilliom, R.; Hogue, T. S.; McCray, J. E.

2017-12-01

There is a need for improved parameterization of stormwater best management practices (BMP) performance estimates to improve modeling of urban hydrology, planning and design of green infrastructure projects, and water quality crediting for stormwater management. Percent removal is commonly used to estimate BMP pollutant removal efficiency, but there is general agreement that this approach has significant uncertainties and is easily affected by site-specific factors. Additionally, some fraction of monitored BMPs have negative percent removal, so it is important to understand the probability that a BMP will provide the desired water quality function versus exacerbating water quality problems. The widely used k-C* equation has shown to provide a more adaptable and accurate method to model BMP contaminant attenuation, and previous work has begun to evaluate the strengths and weaknesses of the k-C* method. However, no systematic method exists for obtaining first-order removal rate constants needed to use the k-C* equation for stormwater BMPs; thus there is minimal application of the method. The current research analyzes existing water quality data in the International Stormwater BMP Database to provide screening-level parameterization of the k-C* equation for selected BMP types and analysis of factors that skew the distribution of efficiency estimates from the database. Results illustrate that while certain BMPs are more likely to provide desired contaminant removal than others, site- and design-specific factors strongly influence performance. For example, bioretention systems show both the highest and lowest removal rates of dissolved copper, total phosphorous, and total nitrogen. Exploration and discussion of this and other findings will inform the application of the probabilistic pollutant removal rate constants. Though data limitations exist, this research will facilitate improved accuracy of BMP modeling and ultimately aid decision-making for stormwater quality

Physicochemical properties of metal-doped activated carbons and relationship with their performance in the removal of SO{sub 2} and NO

Energy Technology Data Exchange (ETDEWEB)

Gao Xiang, E-mail: xgao1@zju.edu.cn [State Key Laboratory of Clean Energy Utilization, Zhejiang University, 38 Zheda Road, Hangzhou 310027 (China); Liu Shaojun; Zhang Yang; Luo Zhongyang; Cen Kefa [State Key Laboratory of Clean Energy Utilization, Zhejiang University, 38 Zheda Road, Hangzhou 310027 (China)

2011-04-15

Research highlights: {yields} Cu and Fe were partly reduced by carbon during preparation. {yields} Metal-involved SO{sub 2} removal pathways were catalytic oxidation, reaction and adsorption. {yields} Good performances of SO{sub 2} and NO removal depended on the metal redox pairs. - Abstract: Several metal-doped activated carbons (Fe, Co, Ni, V, Mn, Cu and Ce) were prepared and characterized. The results of N{sub 2} adsorption-desorption, X-ray diffraction, and X-ray photoelectron spectroscopy indicated that some metals (Cu and Fe) were partly reduced by carbon during preparation. Activity tests for the removal of SO{sub 2} and the selective catalytic reduction of NO with ammonia were carried out. Due to different physicochemical properties, different pathways for the SO{sub 2} removal had been put out, i.e., catalytic oxidation, direct reaction and adsorption. This classification depended on the standard reduction potentials of metal redox pairs. Samples impregnated with V, Ce and Cu showed good activity for NO reduction by NH{sub 3}, which was also ascribed to the reduction potential values of metal redox pairs. Ce seemed to be a promising alternative to V due to the higher activity in NO reduction and the nontoxic property. A metal cation which could easily convert between the two valences seemed to be crucial to the good performance of both SO{sub 2} and NO removal, just like V and Cu.

Nutrients removal in hybrid fluidised bed bioreactors operated with aeration cycles.

Science.gov (United States)

Martin, Martin; Enríquez, L López; Fernández-Polanco, M; Villaverde, S; Garcia-Encina, P A

2007-01-01

Abstract Two hybrid fluidised bed reactors filled with sepiolite and granular activated carbon (GAC) were operated with short cycled aeration for removing organic matter, total nitrogen and phosphorous, respectively. Both reactors were continuously operated with synthetic and/or industrial wastewater containing 350-500 mg COD/L, 110-130 mg NKT/L, 90-100 mg NH3-N/L and 12-15 mg P/L for 8 months. The reactor filled with sepiolite, treating only synthetic wastewater, removed COD, ammonia, total nitrogen and phosphorous up to 88, 91, 55 and 80% with a hydraulic retention time (HRT) of 10 h, respectively. These efficiencies correspond to removal rates of 0.95 kgCODm(-3)d(-1) and 0.16 kg total N m(-3)d(-1). The reactor filled with GAC was operated for 4 months with synthetic wastewater and 4 months with industrial wastewater, removing 98% of COD, 96% of ammonia, and 66% of total nitrogen, with an HRT of 13.6 h. No significant phosphorous removing activity was observed in this reactor. Microbial communities growing with both reactors were followed using polymerase chain reaction (PCR) and denaturing gradient gel electrophoresis (DGGE) techniques. The microbial fingerprints, i.e. DGGE profiles, indicated that biological communities in both reactors were stable along the operational period even when the operating conditions were changed.

Selective near-UV ablation of subgingival dental calculus: measurement of removal rates

Science.gov (United States)

Schoenly, J. E.; Seka, W.; Rechmann, P.

2010-02-01

A noncontact profilometer (laser triangulation) was used to measure the removal rates of subgingival dental calculus irradiated with a frequency-doubled Ti:sapphire laser (60-ns pulse duration, 400-nm wavelength, 10-Hz repetition rate, 7-mJ pulse energy). Profilometer traces before and after irradiation were used to create a removal map with 4-μm axial and 15-μm transverse resolution. Twenty-three teeth (15 with calculus and 8 pristine) were irradiated at 90° and 45° under a cooling water spray with a super-Gaussian beam (~300-μm diameter). Subgingival calculus was selectively removed at 5.6 and 4.0 J/cm2 for 90° and 45°, respecetively, within a range of rates, between 2 to 9 μm/pulse. These ablation rates were constant during these exposures. For comparison, pristine cementum irradiated for 10 min at the same peak fluence and pulse repetition rate showed only craters, 15 to 50 μm deep, corresponding to an equivalent removal rate three orders of magnitude smaller than that obtained for calculus. Pristine enamel was not removed under the same irradiation conditions.

[Pr2(pdc3(Hpdc(H2O4]n·n(H3hp·8n(H2O, a One-Dimensional Coordination Polymer Containing PrO6N3 Tri-Capped Trigonal Prisms and PrO8N Mono-Capped Square Anti-Prisms (H2pdc = Pyridine 2,6-Dicarboxylic Acid, C7H5NO4; 3hp = 3-Hydroxy Pyridine, C5H5NO

Directory of Open Access Journals (Sweden)

Shahzad Sharif

2012-08-01

Full Text Available The synthesis, structure and some properties of the one-dimensional coordination polymer, [Pr2(pdc3(Hpdc]n·n(H3hp·8n(H2O, (H2pdc = pyridine 2,6-dicarboxylic acid, C7H5NO4; 3hp = 3-hydroxypyridine, C5H5NO are described. One of the Pr3+ ions is coordinated by two O,N,O-tridentate pdc2− ligands and one tridentate Hpdc− anion to generate a fairly regular PrO6N3 tri-capped trigonal prism, with the N atoms acting as the caps. The second Pr3+ ion is coordinated by one tridentate pdc2− dianion, four water molecules and two monodentate bridging pdc2− ligands to result in a PrO8N coordination polyhedron that approximates to a mono-capped square-anti-prism. The ligands bridge the metal-atom nodes into a chain, which extends in the [100] direction. The H3hp+ cation and uncoordinated water molecules occupy the inter-chain regions and an N–HLO and numerous O–HLO hydrogen bonds consolidate the structure. The H3hp+ species appears to intercalate between pendant pdc rings to consolidate the polymeric structure. Crystal data: 1 (C33H43N5O29Pr2, Mr = 1255.54, triclinic,  (No. 2, Z = 2, a = 13.2567(1 Å, b = 13.6304(2 Å, c = 13.6409(2 Å, α = 89.695(1°, β = 63.049(1°, γ = 86.105(1°, V = 2191.16(5 Å3, R(F = 0.033, wR(F2 = 0.084.

A performance study of simultaneous microbial removal of no and SO2 in a biotrickling-filter under anaerobic condition

Directory of Open Access Journals (Sweden)

Yaqiong Han

2011-06-01

Full Text Available The behaviors of simultaneous removal of NO and SO2 using the coculture of anaerobic denitrifying bacteria and sulfate reducing bacteria was investigated in a bench-scale biotrickling-filter. When the combined NO/SO2 removal biotrickling-filter was operated at an empty bed residence time of 76 s with NO and SO2 feed concentrations of 2 and 2 g/m3, respectively, the SO2 removal efficiency was always above 95%, while NO removal exhibited an evident periodicity of 5-6 days for the initial 60 days after the attachment phase. A steady-state NO-removal efficiency of around 90% was obtained after 130 days of continuous operation. Experimental results indicated that the coculture in the combined NO/SO2 removal biotrickling-filter showed a higher resistance to shock NO-loadings and a better tolerance to starvation than the single denitrifying bacteria in the NO removal biotrickling-filter.

Rates of calcium carbonate removal from soils.

NARCIS (Netherlands)

Breemen, van N.; Protz, R.

1988-01-01

Mean annual rates of calcium carbonate removal from soils in a subarctic climate estimated from data on two chronosequences of calcareous storm ridges, appeared to be relatively constant through time. Concentrations of dissolved calcium carbonate in the soil solution in the study sites calculated

Forest soil CO2 fluxes as a function of understory removal and N-fixing species addition.

Science.gov (United States)

Li, Haifang; Fu, Shenglei; Zhao, Hongting; Xia, Hanping

2011-01-01

We report on the effects of forest management practices of understory removal and N-fixing species (Cassia alata) addition on soil CO2 fluxes in an Eucalyptus urophylla plantation (EUp), Acacia crassicarpa plantation (ACp), 10-species-mixed plantation (Tp), and 30-species-mixed plantation (THp) using the static chamber method in southern China. Four forest management treatments, including (1) understory removal (UR); (2) C. alata addition (CA); (3) understory removal and replacement with C. alata (UR+CA); and (4) control without any disturbances (CK), were applied in the above four forest plantations with three replications for each treatment. The results showed that soil CO2 fluxes rates remained at a high level during the rainy season (from April to September), followed by a rapid decrease after October reaching a minimum in February. Soil CO2 fluxes were significantly higher (P plantations under various management practices.

n-3 Polyunsaturated Fatty Acid Supplementation Has No Effect on Postprandial Triglyceride-Rich Lipoprotein Kinetics in Men with Type 2 Diabetes

Directory of Open Access Journals (Sweden)

André J. Tremblay

2016-01-01

Full Text Available Dietary n-3 polyunsaturated fatty acids (PUFAs have been proposed to modulate plasma lipids, lipoprotein metabolism, and inflammatory state and to reduce triglyceride (TG concentrations. The present double-blind, randomized, placebo-controlled, crossover study investigated the effects of n-3 PUFA supplementation at 3 g/d for 8 weeks on the intravascular kinetics of intestinally derived apolipoprotein (apo B-48-containing lipoproteins in 10 men with type 2 diabetes. In vivo kinetics of the TG-rich lipoprotein (TRL apoB-48 and VLDL apoB-100 were assessed using a primed-constant infusion of L-[5,5,5-D3] leucine for 12 hours in a fed state. Compared with the placebo, n-3 PUFA supplementation significantly reduced fasting TG concentrations by −9.7% (P=0.05 but also significantly increased plasma levels of cholesterol (C (+6.0%, P=0.05, LDL-C (+12.2%, P=0.04, and HDL-C (+8.4, P=0.007. n-3 PUFA supplementation had no significant impact on postprandial TRL apoB-48 and VLDL apoB-100 levels or on the production or catabolic rates of these lipoproteins. These data indicate that 8-week supplementation with n-3 PUFAs in men with type 2 diabetes has no beneficial effect on TRL apoB-48 and VLDL apoB-100 levels or kinetics.

Nitrogen removal and greenhouse gas emissions from constructed wetlands receiving tile drainage water.

Science.gov (United States)

Groh, Tyler A; Gentry, Lowell E; David, Mark B

2015-05-01

Loss of nitrate from agricultural lands to surface waters is an important issue, especially in areas that are extensively tile drained. To reduce these losses, a wide range of in-field and edge-of-field practices have been proposed, including constructed wetlands. We re-evaluated constructed wetlands established in 1994 that were previously studied for their effectiveness in removing nitrate from tile drainage water. Along with this re-evaluation, we measured the production and flux of greenhouse gases (GHGs) (CO, NO, and CH). The tile inlets and outlets of two wetlands were monitored for flow and N during the 2012 and 2013 water years. In addition, seepage rates of water and nitrate under the berm and through the riparian buffer strip were measured. Greenhouse gas emissions from the wetlands were measured using floating chambers (inundated fluxes) or static chambers (terrestrial fluxes). During this 2-yr study, the wetlands removed 56% of the total inlet nitrate load, likely through denitrification in the wetland. Some additional removal of nitrate occurred in seepage water by the riparian buffer strip along each berm (6.1% of the total inlet load, for a total nitrate removal of 62%). The dominant GHG emitted from the wetlands was CO, which represented 75 and 96% of the total GHG emissions during the two water years. The flux of NO contributed between 3.7 and 13% of the total cumulative GHG flux. Emissions of NO were 3.2 and 1.3% of the total nitrate removed from wetlands A and B, respectively. These wetlands continue to remove nitrate at rates similar to those measured after construction, with relatively little GHG gas loss. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

Collisional Removal of O2 (c(sup 1) Sigma(sup-)(sub u), nu=9) by O2, N2, and He

Science.gov (United States)

Copeland, Richard A.; Knutsen, Karen; Onishi, Marc E.; Yalcin, Talat

1996-01-01

The collisional removal Of 02 molecules in selected vibrational levels of the c state is studied using a two-laser double-resonance technique. The output of the first laser excites the 02 to nu = 9 or 10 of the c Sigma - state, and the ultraviolet output of the second laser monitors specific rovibrational levels via resonance-enhanced ionization. The temporal evolution of the c Sigma u state vibrational level is observed by scanning the time delay between the two pulsed lasers. As the rate constants for 02 and N2 are similar in magnitude, N2 collisions dominate the removal rate in the earth's atmosphere. For v= 10 colliding with 02, we find a removal rate constant that is 2-5 times that for v=9 and that single quantum collision cascade is an important pathway for removal.

NO3 radical measurements in a polluted marine environment: links to ozone formation

Directory of Open Access Journals (Sweden)

J. D. Halla

2010-05-01

Full Text Available Nighttime chemistry in polluted regions is dominated by the nitrate radical (NO3 including its direct reaction with natural and anthropogenic hydrocarbons, its reaction with NO2 to form N2O5, and subsequent reactions of N2O5 to form HNO3 and chlorine containing photolabile species. We report nighttime measurements of NO3, NO2, and O3, in the polluted marine boundary layer southwest of Vancouver, BC during a three week study in the summer of 2005. The concentration of N2O5 was calculated using the well known equilibrium, NO3+NO2↔N2O5. Median overnight mixing ratios of NO3, N2O5 and NO2 were 10.3 ppt, 122 ppt and 8.3 ppb with median N2O5/NO3 molar ratios of 13.1 and median nocturnal partitioning of 4.9%. Due to the high levels of NO2 that can inhibit approach to steady-state, we use a method for calculating NO3 lifetimes that does not assume the steady-state approximation. Median and average lifetimes of NO3 in the NO3-N2O5 nighttime reservoir were 1.1–2.3 min. We have determined nocturnal profiles of the pseudo first order loss coefficient of NO3 and the first order loss coefficients of N2O5 by regression of the NO3 inverse lifetimes with the [N2O5]/[NO3] ratio. Direct losses of NO3 are highest early in the night, tapering off as the night proceeds. The magnitude of the first order loss coefficient of N2O5 is consistent with, but not verification of, recommended homogeneous rate coefficients for reaction of N2O5 with water vapor early in the night, but increases significantly in the latter part of the night when relative humidity increases beyond 75%, consistent with heterogeneous reactions of N2O5 with aerosols with a rate constant khet=(1.2±0.4×10−3 s−1−(1.6±0.4×10−3 s−1. Analysis indicates that a correlation exists between overnight integrated N2O5 concentrations in the marine boundary layer, a surrogate for the accumulation of chlorine containing photolabile species, and maximum 1-h average O3 at stations in the Lower Fraser

No-carrier-added (NCA) N-(3-[18F]fluoropropyl)-N-norbuprenorphine and N-(3-[18F]fluoropropyl)-N-nordiprenorphine -synthesis, anatomical distribution in mice and rats, and tomographic studies in a baboon

International Nuclear Information System (INIS)

Lanqin Bai; Renrui Teng; Chyngyann Shiue; Wolf, A.P.; Dewey, S.L.; Holland, M.J.; Simon, E.J.

1990-01-01

N-(3-Fluoropropyl)-N-norbuprenorphine (3a) and N-(3-fluoropropyl)-N-nordiprenorphine (4a) were synthesized by N-alkylation of norbuprenorphine (1) and nordiprenorphine (2) with 1-bromo-3-fluoropropane. The corresponding no-carrier-added (NCA) N-(3-[ 18 F]fluoropropyl)-N-norbuprenorphine (3b) and N-(3-[ 18 F]fluoropropyl)-N-nordiprenorphine (4b) were synthesized by N-alkylation of 1 and 2 with NCA 1-[ 18 F]fluoro-3-iodopropane. In vitro studies indicate that in the absence of sodium chloride, compounds 3a, 4a, N-propyl-N-norbuprenorphine (5), buprenorphine and diprenorphine are reasonably comparable in binding affinity for opioid receptors. In the presence of 100 mM sodium chloride, however, compounds 3a, 4a and 5, are clearly less potent than buprenorphine and diprenorphine. The anatomical distribution study of compound 3b in mice shows radioactivity accumulating in bone. Rat studies of both compounds 3b and 4b indicate the specific distribution of these two radioligands within certain cortical and subcortical regions of rat brain. However, the absolute uptake of compound 4b in rat brain was only half that of compound 3b. PET studies of 3b in a baboon revealed specific binding of compound 3b in striatum and cerebellum. At 1 h after injection, ratios of specific/non-specific binding of 3b in striatum and cerebellum of a baboon were 1.9 and 1.7 respectively. (author)

Reassessment of the NH4 NO3 thermal decomposition technique for calibration of the N2 O isotopic composition.

Science.gov (United States)

Mohn, Joachim; Gutjahr, Wilhelm; Toyoda, Sakae; Harris, Eliza; Ibraim, Erkan; Geilmann, Heike; Schleppi, Patrick; Kuhn, Thomas; Lehmann, Moritz F; Decock, Charlotte; Werner, Roland A; Yoshida, Naohiro; Brand, Willi A

2016-09-08

In the last few years, the study of N 2 O site-specific nitrogen isotope composition has been established as a powerful technique to disentangle N 2 O emission pathways. This trend has been accelerated by significant analytical progress in the field of isotope-ratio mass-spectrometry (IRMS) and more recently quantum cascade laser absorption spectroscopy (QCLAS). Methods The ammonium nitrate (NH 4 NO 3 ) decomposition technique provides a strategy to scale the 15 N site-specific (SP ≡ δ 15 N α - δ 15 N β ) and bulk (δ 15 N bulk  = (δ 15 N α  + δ 15 N β )/2) isotopic composition of N 2 O against the international standard for the 15 N/ 14 N isotope ratio (AIR-N 2 ). Within the current project 15 N fractionation effects during thermal decomposition of NH 4 NO 3 on the N 2 O site preference were studied using static and dynamic decomposition techniques. The validity of the NH 4 NO 3 decomposition technique to link NH 4 + and NO 3 - moiety-specific δ 15 N analysis by IRMS to the site-specific nitrogen isotopic composition of N 2 O was confirmed. However, the accuracy of this approach for the calibration of δ 15 N α and δ 15 N β values was found to be limited by non-quantitative NH 4 NO 3 decomposition in combination with substantially different isotope enrichment factors for the conversion of the NO 3 - or NH 4 + nitrogen atom into the α or β position of the N 2 O molecule. The study reveals that the completeness and reproducibility of the NH 4 NO 3 decomposition reaction currently confine the anchoring of N 2 O site-specific isotopic composition to the international isotope ratio scale AIR-N 2 . The authors suggest establishing a set of N 2 O isotope reference materials with appropriate site-specific isotopic composition, as community standards, to improve inter-laboratory compatibility. This article is protected by copyright. All rights reserved.

Efficient Total Nitrogen Removal in an Ammonia Gas Biofilter through High-Rate OLAND

DEFF Research Database (Denmark)

De Clippeleir, Haydée; Courtens, Emilie; Mosquera, Mariela

2012-01-01

Ammonia gas is conventionally treated in nitrifying biofilters; however, addition of organic carbon to perform post-denitrification is required to obtain total nitrogen removal. Oxygen-limited autotrophic nitrification/denitrification (OLAND), applied in full-scale for wastewater treatment, can...... offer a cost-effective alternative for gas treatment. In this study, the OLAND application thus was broadened toward ammonia loaded gaseous streams. A down flow, oxygen-saturated biofilter (height of 1.5 m; diameter of 0.11 m) was fed with an ammonia gas stream (248 ± 10 ppmv) at a loading rate of 0...... at water flow rates of 1.3 ± 0.4 m3 m–2 biofilter section d–1. Profile measurements revealed that 91% of the total nitrogen activity was taking place in the top 36% of the filter. This study demonstrated for the first time highly effective and sustainable autotrophic ammonia removal in a gas biofilter...

Relating N2O emissions during biological nitrogen removal with operating conditions using multivariate statistical techniques.

Science.gov (United States)

Vasilaki, V; Volcke, E I P; Nandi, A K; van Loosdrecht, M C M; Katsou, E

2018-04-26

Multivariate statistical analysis was applied to investigate the dependencies and underlying patterns between N 2 O emissions and online operational variables (dissolved oxygen and nitrogen component concentrations, temperature and influent flow-rate) during biological nitrogen removal from wastewater. The system under study was a full-scale reactor, for which hourly sensor data were available. The 15-month long monitoring campaign was divided into 10 sub-periods based on the profile of N 2 O emissions, using Binary Segmentation. The dependencies between operating variables and N 2 O emissions fluctuated according to Spearman's rank correlation. The correlation between N 2 O emissions and nitrite concentrations ranged between 0.51 and 0.78. Correlation >0.7 between N 2 O emissions and nitrate concentrations was observed at sub-periods with average temperature lower than 12 °C. Hierarchical k-means clustering and principal component analysis linked N 2 O emission peaks with precipitation events and ammonium concentrations higher than 2 mg/L, especially in sub-periods characterized by low N 2 O fluxes. Additionally, the highest ranges of measured N 2 O fluxes belonged to clusters corresponding with NO 3 -N concentration less than 1 mg/L in the upstream plug-flow reactor (middle of oxic zone), indicating slow nitrification rates. The results showed that the range of N 2 O emissions partially depends on the prior behavior of the system. The principal component analysis validated the findings from the clustering analysis and showed that ammonium, nitrate, nitrite and temperature explained a considerable percentage of the variance in the system for the majority of the sub-periods. The applied statistical methods, linked the different ranges of emissions with the system variables, provided insights on the effect of operating conditions on N 2 O emissions in each sub-period and can be integrated into N 2 O emissions data processing at wastewater treatment plants

Enzymatic removal of O6-ethylguanine from mitochondrial DNA in rat tissues exposed to N-ethyl-N-nitrosourea in vivo

International Nuclear Information System (INIS)

Satoh, M.S.; Huh, N.; Rajewsky, M.F.; Kuroki, T.

1988-01-01

DNA repair is essential for maintaining the integrity of the genetic material, and a number of DNA repair mechanisms have been fairly well characterized for the nuclear DNA of eukaryotic cells as well as prokaryotes. However, little is know about DNA repair in mitochondria. Using highly sensitive immunoanalytical methods to detect specific DNA alkylation products, the authors found active removal of O 6 -ethyl-2'-deoxyguanosine (O 6 -EtdGuo) from rat liver mitochondrial DNA after pulse-exposure to N-ethyl-N-nitrosourea in vivo. In the kidney, O 6 -EtdGuo was removed from mitochondrial DNA with moderate efficiency, but nearly no removal was observed from the DNA of brain mitochondria. Among the rat tissues examined, the kinetics of O 6 -EtdGuo elimination from mitochondrial DNA was very similar to the kinetics of removal from nuclear DNA. O 4 -Ethyl-2'-deoxythymidine, another premutagenic DNA ethylation product, was stable in both mitochondrial and nuclear DNA of rat liver

Integrated removal of NO and mercury from coal combustion flue gas using manganese oxides supported on TiO2.

Science.gov (United States)

Zhang, Shibo; Zhao, Yongchun; Wang, Zonghua; Zhang, Junying; Wang, Lulu; Zheng, Chuguang

2017-03-01

A catalyst composed of manganese oxides supported on titania (MnO x /TiO 2 ) synthesized by a sol-gel method was selected to remove nitric oxide and mercury jointly at a relatively low temperature in simulated flue gas from coal-fired power plants. The physico-chemical characteristics of catalysts were investigated by X-ray fluorescence (XRF), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) analyses, etc. The effects of Mn loading, reaction temperature and individual flue gas components on denitration and Hg 0 removal were examined. The results indicated that the optimal Mn/Ti molar ratio was 0.8 and the best working temperature was 240°C for NO conversion. O 2 and a proper ratio of [NH 3 ]/[NO] are essential for the denitration reaction. Both NO conversion and Hg 0 removal efficiency could reach more than 80% when NO and Hg 0 were removed simultaneously using Mn0.8Ti at 240°C. Hg 0 removal efficiency slightly declined as the Mn content increased in the catalysts. The reaction temperature had no significant effect on Hg 0 removal efficiency. O 2 and HCl had a promotional effect on Hg 0 removal. SO 2 and NH 3 were observed to weaken Hg 0 removal because of competitive adsorption. NO first facilitated Hg 0 removal and then had an inhibiting effect as NO concentration increased without O 2 , and it exhibited weak inhibition of Hg 0 removal efficiency in the presence of O 2 . The oxidation of Hg 0 on MnO x /TiO 2 follows the Mars-Maessen and Langmuir-Hinshelwood mechanisms. Copyright © 2016. Published by Elsevier B.V.

Removal of retrievable self-expandable urethral stents: experience in 58 stents

International Nuclear Information System (INIS)

Shin, Ji Hoon; Song, Ho-Young; Kim, Jin Hyoung; Ko, Heung-Kyu; Kim, Yong Jae; Woo, Chul-Woong; Kim, Tae-Hyung; Ko, Gi-Young; Yoon, Hyun-Ki; Sung, Kyu-Bo; Park, Hyungkeun

2006-01-01

The purpose of this study was to retrospectively evaluate the safety and efficacy of removing retrievable self-expandable urethral stents using a retrieval hook wire. Under fluoroscopic guidance, the removal of 58 polyurethane or PTFE (polytetrafluoroethylene)-covered stents was attempted in 33 patients using a retrieval hook wire. Indications for removal were elective removal (n=21), stent migration (n=19), formation of tissue hyperplasia around or inside of the stent (n=14), stent deformity (n=3), and severe pain (n=1). The mean time the stents remained in place was 64.8±42.9 days (range, 1-177 days). Fifty-six (97%) of the 58 stents were successfully removed using the retrieval hook wire despite the following difficulties; hook wire disconnection (n=2), untied drawstrings (n=3), and polyurethane membrane disruption/separation (n=4). The removal procedure using a retrieval hook wire failed in two stents (3%) which had migrated into the urinary bladder. One of the two stents with migration into the urinary bladder was removed using a snare through the cystostomy route. The overall complication rate was 14% (seven hematuria cases and one urethral tear case), and all were minor and spontaneously resolved without further treatment. In conclusion, removal of retrievable urethral stents using a retrieval hook wire was safe and effective despite some technical difficulties. It is a useful method for allowing temporary stent placement and solving various complications of stent use. (orig.)

Removal of retrievable self-expandable urethral stents: experience in 58 stents

Energy Technology Data Exchange (ETDEWEB)

Shin, Ji Hoon; Song, Ho-Young; Kim, Jin Hyoung; Ko, Heung-Kyu; Kim, Yong Jae; Woo, Chul-Woong; Kim, Tae-Hyung; Ko, Gi-Young; Yoon, Hyun-Ki; Sung, Kyu-Bo [Asan Medical Center, Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Seoul (Korea); Park, Hyungkeun [Asan Medical Center, Department of Urology, University of Ulsan College of Medicine, Seoul (Korea)

2006-09-15

The purpose of this study was to retrospectively evaluate the safety and efficacy of removing retrievable self-expandable urethral stents using a retrieval hook wire. Under fluoroscopic guidance, the removal of 58 polyurethane or PTFE (polytetrafluoroethylene)-covered stents was attempted in 33 patients using a retrieval hook wire. Indications for removal were elective removal (n=21), stent migration (n=19), formation of tissue hyperplasia around or inside of the stent (n=14), stent deformity (n=3), and severe pain (n=1). The mean time the stents remained in place was 64.8{+-}42.9 days (range, 1-177 days). Fifty-six (97%) of the 58 stents were successfully removed using the retrieval hook wire despite the following difficulties; hook wire disconnection (n=2), untied drawstrings (n=3), and polyurethane membrane disruption/separation (n=4). The removal procedure using a retrieval hook wire failed in two stents (3%) which had migrated into the urinary bladder. One of the two stents with migration into the urinary bladder was removed using a snare through the cystostomy route. The overall complication rate was 14% (seven hematuria cases and one urethral tear case), and all were minor and spontaneously resolved without further treatment. In conclusion, removal of retrievable urethral stents using a retrieval hook wire was safe and effective despite some technical difficulties. It is a useful method for allowing temporary stent placement and solving various complications of stent use. (orig.)

A novel method of simultaneous NH4+ and NO3- removal using Fe cycling as a catalyst: Feammox coupled with NAFO.

Science.gov (United States)

Li, Xiang; Yuan, Yan; Huang, Yong; Liu, Heng-Wei; Bi, Zhen; Yuan, Yi; Yang, Peng-Bin

2018-08-01

The feasibility of using Feammox coupled with nitrate-dependent Fe(II) oxidizing (NAFO) to cause the simultaneous conversion of NH 4 + and NO 3 - was explored by inoculation with Feammox sludge and the use Fe cycling as catalyst. After 61days operation, the simultaneous conversion of NO 3 - and NH 4 + occurred with the presence of interconversion between Fe(III) and Fe(II). The conversion ratio of NH 4 + to NO 3 - stabilized at 0.9-1. The results of isotopic tracing and microbial diversity analysis indicated that NH 4 + was first oxidized to NO 2 - by Fe(III), then NO 3 - was reduced to NO 2 - and N 2 by the Fe(II) produced in Feammox process, and finally, the NO 2 - produced in NAFO process underwent an Anammox process with the remaining NH 4 + to yield N 2 . The results showed the simultaneous continuous conversion process of NO 3 - and NH 4 + with limited Fe as a catalyst was a coupled process of Feammox, Anammox, and NAFO under the anaerobic conditions. Copyright © 2018 Elsevier B.V. All rights reserved.

Acción de distintos coagulantes para la eliminación de Cryptosporidium spp. en el proceso de potabilización del agua The action of different coagulants to remove Cryptosporidium during the process of water treatment

Directory of Open Access Journals (Sweden)

B. Abramovich

2004-06-01

Full Text Available Cryptosporidium es uno de los microorganismos de mayor interés desde el punto de vista de la Salud Pública y constituye un problema prioritario para las plantas y organismos reguladores de agua. Debido a su pequeño tamaño y a su resistencia a la cloración, la eliminación por el proceso de potabilización es una tarea compleja. En este trabajo se analizó la efectividad de distintos coagulantes utilizados comúnmente en tal proceso para lograr la remoción de los ooquistes. Se trabajó con la prueba de jarras (Jar Test. Se halló que: 1 Los coagulantes con agregado de polímeros coadyuvantes producen remociones de ooquistes superiores a 2 log. 2 Un valor bajo de turbiedad no asegura una remoción óptima de los parásitos. 3 La adición de polielectrolitos al cloruro férrico disminuye la variabilidad tanto en la turbiedad final como en la eliminación de Cryptosporidium.Cryptosporidium is one of the microorganisms of main concern from the point of view of Public Health, being a priority problem for water treatment plants and water regulatory institutions. Due to its small size and resistance to chlorination, Cryptosporidium removal during the process of drinking water treatmentis a hard task. The effectiveness of different coagulants commonly used in the process of removal of oocysts was analyzed. Thetechnique used was the Jar Test. It was found that: 1 coagulants with the addition of polimeric coadjuvants produce over 2 logs of oocyst removal; 2 a low value in turbidity does not necessarily mean optimal parasite removal, and 3 the addition of polyelectrolites to ferric chloride diminishes variability, both in final turbidity and Cryptosporidium removal.

Functional clay supported bimetallic nZVI/Pd nanoparticles used for removal of methyl orange from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Wang, Ting [School of Environmental Science and Engineering, Fujian Normal University, Fuzhou 350007, Fujian Province (China); Fujian Key Laboratory of Pollution Control and Resource Reuse, Fujian Normal University, Fuzhou 350007, Fujian Province (China); Su, Jin [School of Environmental Science and Engineering, Fujian Normal University, Fuzhou 350007, Fujian Province (China); Jin, Xiaoying [School of Environmental Science and Engineering, Fujian Normal University, Fuzhou 350007, Fujian Province (China); Fujian Key Laboratory of Pollution Control and Resource Reuse, Fujian Normal University, Fuzhou 350007, Fujian Province (China); Chen, Zuliang, E-mail: Zuliang.chen@unisa.edu.au [School of Environmental Science and Engineering, Fujian Normal University, Fuzhou 350007, Fujian Province (China); Centre for Environmental Risk Assessment and Remediation, University of South Australia, Mawson Lakes, SA 5095 (Australia); Megharaj, Mallavarapu; Naidu, Ravendra [Centre for Environmental Risk Assessment and Remediation, University of South Australia, Mawson Lakes, SA 5095 (Australia)

2013-11-15

Highlights: • Functional clay supported bimetallic nZVI/Pd was synthesized. • Methyl orange (MO) was degraded using B-nZVI/Pd. • 93.75% of MO in wastewater was removed. • The functions of clay, nZVI and Pd were observed. -- Abstract: Bentonite supported Fe/Pd nanoparticles (B/nZVI/Pd) were synthesized as composites that exhibit functionalities assisting in the removal of methyl orange (MO) from aqueous solution. The results showed that 91.87% of MO was removed using B/nZVI/Pd, while only 85% and 1.41% of MO were removed using nZVI/Pd and bentonite after 10 min, respectively. The new findings include that the presence of bentonite decreased the aggregation of nZVI/Pd and nZVI in the composite played its role as a reductant, while Pd{sup 0} acted as the catalyst to enhance the degradation of MO, which were confirmed by scanning electron microscopy (SEM), X-ray diffraction (XRD), UV–vis analysis and the batch experiments. The increase in B/nZVI/Pd loading led to greater removal efficiency, while decolorization efficiency declined in the presence of anions such as nitrate, sulfite and carbonate, especially nitrate, which decreased the apparent rate constant k{sub obs} almost 17.06-fold. The kinetics study indicated that the degradation of MO fitted well to the pseudo-first-order model, where the k{sub obs} was 0.0721 min{sup −1}. Finally, the reactivity of aged B/nZVI/Pd was investigated, and the application of B/nZVI/Pd in wastewater indicated a removal efficiency higher than 93.75%. This provided a new environmental pollution management option for dyes-contaminated sites.

[KDy(Hptc3(H3ptc]n·2n(Hbipy·5n(H2O, a Layered Coordination Polymer Containing DyO6N3 Tri-Capped Trigonal Prisms (H3ptc = Pyridine 2,4,6-Tricarboxylic Acid, C8H5NO6; Bipy = 2,2'-Bipyridine, C10H8N2

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Shoaib Anwar

2012-08-01

Full Text Available The synthesis, structure and properties of the bimetallic layered coordination polymer, [KDy(C8H3NO63(C8H5NO6]n·2n(C10H9N2·5n(H2O = [KDy(Hptc3(H3ptc]n·2n(Hbipy·5n(H2O, are described. The Dy3+ ion is coordinated by three O,N,O-tridentate doubly-deprotonated pyridine tri-carboxylate (Hptc ligands to generate a fairly regular DyO6N3 tri-capped trigonal prism, with the N atoms acting as the caps. The potassium ion is coordinated by an O,N,O-tridentate H3ptc molecule as well as monodentate and bidentate Hptc ligands to result in an irregular KNO9 coordination geometry. The ligands bridge the metal-atom nodes into a bimetallic, layered, coordination polymer, which extends as corrugated layers in the (010 plane, with the mono-protonated bipyridine cations and water molecules occupying the inter-layer regions: Unlike related structures, there are no dysprosium–water bonds. Many O–HLO and N–HLO hydrogen bonds consolidate the structure. Characterization and bioactivity data are described. Crystal data: C52H42DyKN8O29, Mr = 1444.54, triclinic,  (No. 2, Z = 2, a = 9.188(2 Å, b = 15.7332(17 Å, c = 19.1664(19 Å, α = 92.797(6°, β = 92.319(7°, γ = 91.273(9°, V = 2764.3(7 Å3, R(F = 0.029, wR(F2 = 0.084.

Comparison of N2O5 mixing ratios during NO3Comp 2007 in SAPHIR

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A. W. Rollins

2012-11-01

Full Text Available N2O5 detection in the atmosphere has been accomplished using techniques which have been developed during the last decade. Most techniques use a heated inlet to thermally decompose N2O5 to NO3, which can be detected by either cavity based absorption at 662 nm or by laser-induced fluorescence. In summer 2007, a large set of instruments, which were capable of measuring NO3 mixing ratios, were simultaneously deployed in the atmosphere simulation chamber SAPHIR in Jülich, Germany. Some of these instruments measured N2O5 mixing ratios either simultaneously or alternatively. Experiments focused on the investigation of potential interferences from, e.g., water vapour or aerosol and on the investigation of the oxidation of biogenic volatile organic compounds by NO3. The comparison of N2O5 mixing ratios shows an excellent agreement between measurements of instruments applying different techniques (3 cavity ring-down (CRDS instruments, 2 laser-induced fluorescence (LIF instruments. Datasets are highly correlated as indicated by the square of the linear correlation coefficients, R2, which values were larger than 0.96 for the entire datasets. N2O5 mixing ratios well agree within the combined accuracy of measurements. Slopes of the linear regression range between 0.87 and 1.26 and intercepts are negligible. The most critical aspect of N2O5 measurements by cavity ring-down instruments is the determination of the inlet and filter transmission efficiency. Measurements here show that the N2O5 inlet transmission efficiency can decrease in the presence of high aerosol loads, and that frequent filter/inlet changing is necessary to quantitatively sample N2O5 in some environments. The analysis of data also demonstrates that a general correction for degrading filter transmission is not applicable for all conditions encountered during this campaign. Besides the effect of a gradual degradation of the inlet transmission efficiency aerosol exposure, no other interference

Effects of particulates, heavy metals and acid gas on the removals of NO and PAHs by V2O5-WO3 catalysts in waste incineration system

International Nuclear Information System (INIS)

Chang, Feng-Yim; Chen, Jyh-Cherng; Wey, Ming-Yen; Tsai, Shih-An

2009-01-01

This study investigated the activities of prepared and commercial V 2 O 5 -WO 3 catalysts for simultaneous removals of NO and polycyclic aromatic hydrocarbons (PAHs) and the influences of particulates, heavy metals, SO 2 , and HCl on the performances of catalysts. The experiments were carried out in a laboratory-scale waste incineration system equipped with a catalyst reactor. The DREs of PAHs by prepared and commercial V 2 O 5 -WO 3 catalysts were 64% and 72%, respectively. Increasing the particulate concentrations in flue gas suppressed the DRE of PAHs, but increasing the carbon content on surface of catalysts promotes the NO conversions. The DRE of PAHs by the catalysts was significantly decreased by the increased concentrations of heavy metal Cd, but was promoted by high concentration of Pb. The influence level of SO 2 was higher than HCl on the performances of V 2 O 5 -WO 3 catalysts for PAHs removal, but was lower than HCl for NO removal. Prepared and commercial V 2 O 5 -WO 3 catalysts have similar trends on the effects of particulates, heavy metals, SO 2 , and HCl. The results of ESCA analysis reveal that the presences of these pollutants on the surface of catalysts did not change the chemical state of V and W.

Oxygen Limited Bioreactors System For Nitrogen Removal Using Immobilized Mix Culture

Science.gov (United States)

Pathak, B. K.; Sumino, T.; Saiki, Y.; Kazama, F.

2005-12-01

Recently nutrients concentrations especially nitrogen in natural water is alarming in the world wide. Most of the effort is being done on the removal of high concentration of nitrogen especially from the wastewater treatment plants. The removal efficiency is targeted in all considering the effluent discharge standard set by the national environment agency. In many cases, it does not meet the required standard and receiving water is being polluted. Eutrophication in natural water bodies has been reported even if the nitrogen concentration is low and self purification of natural systems itself is not sufficient to remove the nitrogen due to complex phenomenon. In order to recover the pristine water environment, it is very essential to explore bioreactor systems for natural water systems using immobilized mix culture. Microorganism were entrapped in Polyethylene glycol (PEG) prepolymer gel and cut into 3mm cubic immobilized pellets. Four laboratory scale micro bio-reactors having 0.1 L volumes were packed with immobilized pellets with 50% compact ratio. RUN1, RUN2, RUN3 and RUN4 were packed with immobilized pellets from reservoirs sediments, activated sludge (AS), mixed of AS, AG and biodegradable plastic and anaerobic granules (AG) respectively. Water from Shiokawa Reservoirs was feed to all reactors with supplemental ammonia and nitrite nitrogen as specified in the results and discussions. The reactors were operated dark incubated room in continuous flow mode with hydraulic retention time of 12 hours under oxygen limiting condition. Ammonium, nitrate nitrite nitrogen and total organic carbon (TOC) concentrations were measured as described in APWA and AWWA (1998). Laboratory scale four bioreactors containing different combination of immobilized cell were monitored for 218 days. Influent NH4+-N and NO2--N concentration were 2.27±0.43 and 2.05±0.41 mg/l respectively. Average dissolved oxygen concentration and pH in the reactors were 0.40-2.5 mg/l and pH 6

Lanthanum-promoted copper-based hydrotalcites derived mixed oxides for NO{sub x} adsorption, soot combustion and simultaneous NO{sub x}-soot removal

Energy Technology Data Exchange (ETDEWEB)

Wang, Zhongpeng [School of Resources and Environment, University of Jinan, 106 Jiwei Road, Jinan 250022 (China); Inorganic Chemistry Laboratory, University of Oxford, South Parks Road, Oxford OX1 3QR (United Kingdom); Yan, Xiaotong; Bi, Xinlin; Wang, Liguo [School of Resources and Environment, University of Jinan, 106 Jiwei Road, Jinan 250022 (China); Zhang, Zhaoliang, E-mail: chm_zhangzl@ujn.edu.cn [School of Resources and Environment, University of Jinan, 106 Jiwei Road, Jinan 250022 (China); Jiang, Zheng; Xiao, Tiancun [Inorganic Chemistry Laboratory, University of Oxford, South Parks Road, Oxford OX1 3QR (United Kingdom); Umar, Ahmad [Department of Chemistry, College of Science and Arts, Najran University, P.O. Box 1988, Najran 11001 (Saudi Arabia); Promising Centre for Sensors and Electronic Devices (PCSED), Najran University, P.O. Box 1988, Najran 11001 (Saudi Arabia); Wang, Qiang, E-mail: qiang.wang.ox@gmail.com [College of Environmental Science and Engineering, Beijing Forestry University, 35 Tsinghua East Road, Beijing 100083 (China)

2014-03-01

Graphical abstract: - Highlights: • The addition of La in Cu-based oxides increased the types of active oxygen. • NO{sub x} adsorption, soot oxidation and simultaneous NO{sub x}-soot removal were enhanced. • The possible catalytic mechanism was studied via in situ FTIR analysis. • Soot oxidation was promoted by the NO{sub 2} intermediate. - Abstract: La-promoted Cu-based hydrotalcites derived mixed oxides were prepared and their catalytic activities for NO{sub x} adsorption, soot oxidation, and simultaneous NO{sub x}-soot removal were investigated. The catalysts were characterized by XRD, DTG, BET, FTIR, H2-TPR, TPD and TPO techniques. The oxides catalysts exhibited mesoporous properties with specific surface area of 45–160 m{sup 2}/g. The incorporation of La and Cu decreased the amount of basic sites due to the large decrease in surface areas. Under O{sub 2} atmosphere, La incorporation is dominant for soot oxidation activity, while Cu favors high selectivity to CO{sub 2} formation. A synergetic effect between La and Cu for catalyzed soot oxidation lies in the improved redox property and suitable basicity. The presence of NO in O{sub 2} significantly promoted soot oxidation on the catalysts with the ignition temperature decreased to about 300 °C. In O{sub 2}/NO atmosphere, NO{sub 2} acts as an intermediate which oxidizes soot to CO{sub 2} at a lower temperature with itself reduced to NO or N{sub 2}, contributing to the high catalytic performance in simultaneous removal of NO{sub x} and soot.

Nitrogen-removal performance and community structure of nitrifying bacteria under different aeration modes in an oxidation ditch.

Science.gov (United States)

Guo, Chang-Zi; Fu, Wei; Chen, Xue-Mei; Peng, Dang-Cong; Jin, Peng-Kang

2013-07-01

Oxidation-ditch operation modes were simulated using sequencing batch reactors (SBRs) with alternate stirring and aerating. The nitrogen-removal efficiencies and nitrifying characteristics of two aeration modes, point aeration and step aeration, were investigated. Under the same air-supply capacity, oxygen dissolved more efficiently in the system with point aeration, forming a larger aerobic zone. The nitrifying effects were similar in point aeration and step aeration, where the average removal efficiencies of NH4(+) N were 98% and 96%, respectively. When the proportion of anoxic and oxic zones was 1, the average removal efficiencies of total nitrogen (TN) were 45% and 66% under point aeration and step aeration, respectively. Step aeration was more beneficial to both anoxic denitrification and simultaneous nitrification and denitrification (SND). The maximum specific ammonia-uptake rates (AUR) of point aeration and step aeration were 4.7 and 4.9 mg NH4(+)/(gMLVSS h), respectively, while the maximum specific nitrite-uptake rates (NUR) of the two systems were 7.4 and 5.3 mg NO2(-)-N/(gMLVSS h), respectively. The proportions of ammonia-oxidizing bacteria (AOB) to all bacteria were 5.1% under point aeration and 7.0% under step aeration, and the proportions of nitrite-oxidizing bacteria (NOB) reached 6.5% and 9.0% under point and step aeration, respectively. The dominant genera of AOB and NOB were Nitrosococcus and Nitrospira, which accounted for 90% and 91%, respectively, under point aeration, and the diversity of nitrifying bacteria was lower than under step aeration. Point aeration was selective of nitrifying bacteria. The abundance of NOB was greater than that of AOB in both of the operation modes, and complete transformation of NH4(+) N to NO3(-)-N was observed without NO2(-)-N accumulation. Copyright © 2013 Elsevier Ltd. All rights reserved.

LO POPULAR NO-RATING SOBERANÍA DE LA COMUNICACIÓN POPULAR EN AMÉRICA LATINA

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Víctor Adrián Díaz Esteves

2009-01-01

Full Text Available A partir de un enfoque popular en construcción, este ensayo se propone reflexionar en torno a la noción original de comunicación humana. Asimismo, se aproxima al debate sobre las culturas populares en América Latina, construidas desde los sujetos, caracterizados por dos elementos aparentemente enfrentados, que se entremezclan. Por un lado, los sujetos son consumidores de la oferta rentable y global de los medios masivos; cuya hegemonía responde al rating y al capital. Por otro lado, son productores culturales de sentido e imágenes simbólicas propias, resistentes y en ocasiones, contradictorias. La comunicación popular favorece la producción local y regional; la participación ciudadana, la integración y el cambio social; la igualdad y la democracia. Esta mirada popular de la comunicación, es parte de las mutaciones que la modernidad ha introducido en los países latinoamericanos, y a la vez, define a las culturas populares, no como esa masa homogénea, pasiva y dominada por los mass media, sino conscientes del entrecruzamiento de expresiones sociales, orígenes, gustos, modas y costumbres diversas, en busca de la construcción de comunidades culturales de sentido y respeto en materia de derechos.

Characteristics of NH4+ and NO3- fluxes in tea (Camellia sinensis) roots measured by scanning ion-selective electrode technique.

Science.gov (United States)

Ruan, Li; Wei, Kang; Wang, Liyuan; Cheng, Hao; Zhang, Fen; Wu, Liyun; Bai, Peixian; Zhang, Chengcai

2016-12-05

As a vital beverage crop, tea has been extensively planted in tropical and subtropical regions. Nitrogen (N) levels and forms are closely related to tea quality. Based on different N levels and forms, we studied changes in NO 3 - and NH 4 + fluxes in tea roots utilizing scanning ion-selective electrode technique. Our results showed that under both single and mixed N forms, influx rates of NO 3 - were much lower than those of NH 4 + , suggesting a preference for NH 4 + in tea. With the increase in N concentration, the influx rate of NO 3 - increased more than that of NH 4 + . The NH 4 + influx rates in a solution without NO 3 - were much higher than those in a solution with NO 3 - , while the NO 3 - influx rates in a solution without NH 4 + were much lower than those in a solution with NH 4 + . We concluded that (1) tea roots showed a preference for NH 4 + , (2) presence of NO 3 - had a negative effect on NH 4 + influx, and (3) NH 4 + had a positive effect on NO 3 - influx. Our findings not only may help advance hydroponic tea experiments but also may be used to develop efficient fertilization protocols for soil-grown tea in the future.

Arsenic removal from groundwater using iron electrocoagulation: effect of charge dosage rate.

Science.gov (United States)

Amrose, Susan; Gadgil, Ashok; Srinivasan, Venkat; Kowolik, Kristin; Muller, Marc; Huang, Jessica; Kostecki, Robert

2013-01-01

We demonstrate that electrocoagulation (EC) using iron electrodes can reduce arsenic below 10 μg/L in synthetic Bangladesh groundwater and in real groundwater from Bangladesh and Cambodia, while investigating the effect of operating parameters that are often overlooked, such as charge dosage rate. We measure arsenic removal performance over a larger range of current density than in any other single previous EC study (5000-fold: 0.02 - 100 mA/cm(2)) and over a wide range of charge dosage rates (0.060 - 18 Coulombs/L/min). We find that charge dosage rate has significant effects on both removal capacity (μg-As removed/Coulomb) and treatment time and is the appropriate parameter to maintain performance when scaling to different active areas and volumes. We estimate the operating costs of EC treatment in Bangladesh groundwater to be $0.22/m(3). Waste sludge (~80 - 120 mg/L), when tested with the Toxic Characteristic Leachate Protocol (TCLP), is characterized as non-hazardous. Although our focus is on developing a practical device, our results suggest that As[III] is mostly oxidized via a chemical pathway and does not rely on processes occurring at the anode. Supplementary materials are available for this article. Go to the publisher's online edition of Journal of Environmental Science and Health, Part A, to view the free supplemental file.

Nqrs Data for C3H2Cl10N2PSb[C3HCl4N2P·Cl6HSb](Subst. No. 0601)

Science.gov (United States)

Chihara, H.; Nakamura, N.

This document is part of Subvolume A `Substances Containing Ag … C10H15' of Volume 48 `Nuclear Quadrupole Resonance Spectroscopy Data' of Landolt-Börnstein - Group III `Condensed Matter'. It contains an extract of Section `3.2 Data tables' of the Chapter `3 Nuclear quadrupole resonance data' providing the NQRS data for C3H2Cl10N2PSb [C3HCl4N2P·Cl6HSb] (Subst. No. 0601)

Removal in a lump of JRR-3 nuclear reactor

International Nuclear Information System (INIS)

Ohnishi, Nobuaki; Suzuki, Masanori; Nagase, Tetsuo; Watanabe, Morinari.

1989-01-01

The research reactor JRR-3 in Japan Atomic Energy Research Institute is called 'Home made No.1 reactor' as all except fuel and heavy water as the moderator and coolant were manufactured in Japan. The JRR-3 attained the criticality in 1962, and the cumulative time of operation reached 47135.5 hours, and the cumulative power output reached 419073.5 MWh. It was stopped in 1983. During the period, it was utilized for beam experiment, irradiation of fuel and materials, RI production and others. In order to cope with the expansion of utilization and the advance of utilizing technology of the research reactor, the reconstruction works are in progress, and the criticality of the reconstructed reactor is expected in 1990. On the site where the old reactor is removed, the reactor of different type is installed, and the first large cold neutron source is equipped. In this report, as to the removal of the old reactor proper, the method of working and the results are described. Considering the period of working, the cost and the management of the removed reactor, in the case of the JRR-3, the method of carrying it out in a lump was adopted as the optimum removal method. The plan, procedure and results of the removal working are reported. (K.I.)

Room and high temperature interactions in sodium and rubidium rich ternary nitrate mixtures of UO2(NO3)2.6H2O - NaNO3 - RbNO3

International Nuclear Information System (INIS)

Kalekar, Bhupesh B.; Reddy, A.V.R.; Raje, Naina

2016-01-01

High temperature interaction behavior of nitrates is important for characterizing different intermediate products and their thermal stabilities during the calcination of nuclear waste before their immobilization in the stable glass matrix. Mixtures of UO 2 (NO 3 ) 2 .6H 2 O (UNH) with NaNO 3 (NaN) and RbNO 3 (RbN) were prepared by mixing the weighed amounts of component nitrates and grinding gently in a mortar and pestle. The mixing and grinding of individual nitrate components in a mortar with pestle showed the agglomeration of solid particles and subsequent dissolution probably in the water of crystallization of UNH. The continued grinding and mixing showed the reappearance of the solid powder. The original yellow color of the mixture was changed to greenish yellow color. The mixtures were subjected to thermal measurements using Netzsch Thermobalance (Model No.: STA 409 PC Luxx) coupled to Bruker FTIR system (Model No.: Tensor 27) via a heated Teflon capillary (1 m long, 2 mm i.d.). TG - DTG curves of equimolar mixture are displayed. The plateau was observed on TG curve in the temperature region of 31- 250 °C. It is reported that Na(UO 2 (NO 3 ) 3 ).H 2 O and Rb(UO 2 (NO 3 ) 3 ) formed around 250 °C in the equimolar nitrate mixtures of UNH-NaN and UNH-RbN. Thermal and XRD results indicated the formation of Na(UO 2 (NO 3 ) 3 ).H 2 O and Rb(UO 2 (NO) 3 ) 3 ) even by mixing the UNH, NaN and RbN in equimolar ratios at room temperature

Comparison of nutrient removal capacity and biomass settleability of four high-potential microalgal species.

Science.gov (United States)

Su, Yanyan; Mennerich, Artur; Urban, Brigitte

2012-11-01

Four common used microalgae species were compared in terms of settleability, nutrient removal capacity and biomass productivity. After 1 month training, except cyanobacteria Phormidium sp., three green microalgae species, Chlamydomonas reinhardtii, Chlorella vulgaris and Scenedesmus rubescens, showed good settleability. The N and P removal efficiency was all above 99% within 7, 4, 6 and 6 days for N and 4, 2, 3 and 4 days for P, resulting in the N removal rates of 3.66±0.17, 6.39±0.20, 4.39±0.06 and 4.31±0.18 mg N/l/d and P removal rates of 0.56±0.07, 0.89±0.05, 0.76±0.09 and 0.60±0.05 mg P/l/d for Phormidium sp., C. reinhardtii, C. vulgaris and S. rubescens, respectively. Phormidium sp. had the lowest algal biomass productivity (2.71±0.7 g/m(2)/d) and the other three green microalgae showed higher algal biomass productivity (around 6 g/m(2)/d). Assimilation into biomass was the main removal mechanism for N and P. Copyright © 2012 Elsevier Ltd. All rights reserved.

Photocatalytic oxidation removal of Hg"0 using ternary Ag/AgI-Ag_2CO_3 hybrids in wet scrubbing process under fluorescent light

International Nuclear Information System (INIS)

Zhang, Anchao; Zhang, Lixiang; Chen, Xiaozhuan; Zhu, Qifeng; Liu, Zhichao; Xiang, Jun

2017-01-01

Highlights: • Ag/AgI-Ag_2CO_3 hybrids were employed for Hg"0 removal under fluorescent light. • Superoxide radical (·O_2"−) played a key role in Hg"0 removal. • NO exhibited a significant effect on Hg"0 removal in comparison to SO_2. • The mechanism for enhanced Hg"0 removal over Ag/AgI-Ag_2CO_3 was proposed. - Abstract: A series of ternary Ag/AgI-Ag_2CO_3 photocatalysts synthesized using a facile coprecipitation method were employed to investigate their performances of Hg"0 removal in a wet scrubbing reactor. The hybrids were characterized by N_2 adsorption-desorption, XRD, SEM-EDS, HRTEM, XPS, DRS and ESR. The photocatalytic activities of Hg"0 removal were evaluated under fluorescent light. The results showed that AgI content, fluorescent light irradiation, reaction temperature all showed significant influences on Hg"0 removal. NO exhibited significant effect on Hg"0 removal in comparison to SO_2. Among these ternary Ag/AgI-Ag_2CO_3 hybrids, Ag/AgI(0.1)-Ag_2CO_3 showed the highest Hg"0 removal efficiency, which could be ascribed to the effective separation of photogenerated electron-hole pairs between AgI and Ag_2CO_3 and the surface plasmon resonance (SPR) effect in the visible region by metallic silver nanoparticles (Ag"0 NPs). The trapping studies of reactive radicals showed that the superoxide radicals (·O_2"−) may play a key role in Hg"0 removal under fluorescent light. According to the experimental and characterization results, a possible photocatalytic oxidation mechanism for enhanced Hg"0 removal over Ag/AgI(0.1)-Ag_2CO_3 hybrid under fluorescent light was proposed.

A feasible process for simultaneous removal of CO2, SO2 and NOx in the cement industry by NH3 scrubbing

International Nuclear Information System (INIS)

Dong, Ruifeng; Lu, Hongfang; Yu, Yunsong; Zhang, Zaoxiao

2012-01-01

Highlights: ► Simultaneous removal of CO 2 , SO 2 and NO x is realized by NH 3 scrubbing with NaClO 2 . ► The crystallization process of NH 4 HCO 3 is employed instead of CO 2 regeneration. ► Energy consumption reduces hugely while CO 2 removal rate remains higher than 90%. ► Exergy calculation reveals that a higher thermodynamic perfection degree is achieved. -- Abstract: With the rapid economic and industrial development, the concentration of carbon dioxide in the atmosphere is increasing enormously, which has greatly affected the global climate and human living environment. At present, a lot of technologies have been applied to CO 2 removal in fossil fuel-fired power plants, which are one of the main CO 2 emission sources. But few researches have been done in the cement industry, which is the third largest CO 2 emission source. There is no mature technology of CO 2 removal in cement industry mentioned before. This paper proposes a feasible process for simultaneous removal of CO 2 , SO 2 and NO x in the cement industry by NH 3 scrubbing. As there is no ready steam source for the regeneration of CO 2 -rich loading solvent after absorption, a process with the final product of ammonium bicarbonate is developed. With the oxidative additive of NaClO 2 added in the aqueous ammonium absorbent, the simultaneous removal of CO 2 , SO 2 and NO x is feasible by NH 3 scrubbing. The products of the process are mainly ammonium bicarbonate, ammonium sulfate and ammonium nitrate, which are all good fertilizers for crops and plants. The crystallization of NH 4 HCO 3 is easier for storage and transportation than that for liquid carbon dioxide, which becomes more stable when dicyandiamide (DCD) is added. The thermodynamic analysis proves that the proposed process has the advantages of energy conservation and high thermodynamic perfection degree compared with the traditional ones.

Invasive acacias experience higher ant seed removal rates at the invasion edges

Directory of Open Access Journals (Sweden)

D. Montesinos

2012-06-01

Full Text Available Seed dispersal is a key process for the invasion of new areas by exotic species. Introduced plants often take advantage of native generalist dispersers. Australian acacias are primarily dispersed by ants in their native range and produce seeds bearing a protein and lipid rich reward for ant mutualists (elaiosome. Nevertheless, the role of myrmecochory in the expansion of Australian acacias in European invaded areas is still not clear. We selected one European population of Acacia dealbata and another of A. longifolia and offered elaiosome-bearing and elaiosome-removed seeds to local ant communities. For each species, seeds were offered both in high-density acacia stands and in low-density invasion edges. For both acacia species, seed removal was significantly higher at the low-density edges. For A. longifolia, manual elimination of elaiosomes reduced the chance of seed removal by 80% in the low-density edges, whereas it made no difference on the high-density stands. For A. dealbata, the absence of elaiosome reduced seed removal rate by 52%, independently of the acacia density. Our data suggests that invasive acacias have found effective ant seed dispersers in Europe and that the importance of such dispersers is higher at the invasion edges.

Successful Removal of Football Helmet Face-Mask Clips After 1 Season of Use

Science.gov (United States)

Scibek, Jason S.; Gatti, Joseph M.; McKenzie, Jennifer I.

2012-01-01

Context Whereas many researchers have assessed the ability to remove loop straps in traditional face-mask attachment systems after at least 1 season of use, research in which the effectiveness of the Riddell Quick Release (QR) Face Guard Attachment System clip after 1 season has been assessed is limited. Objective To examine the success rate of removing the QR clips after 1 season of use at the Football Championship Subdivision level. We hypothesized that 1 season of use would negatively affect the removal rate of the QR clip but repeated clip-removal trials would improve the removal rate. Design Retrospective, quasi-experimental design. Setting Controlled laboratory study. Patients or Other Participants Sixty-three football helmets from a National Collegiate Athletic Association Division I university located in western Pennsylvania used during the 2008 season were tested. Intervention(s) Three certified athletic trainers (2 men, 1 woman; age = 31.3 ± 3.06 years, time certified = 9.42 ± 2.65 years) attempted to remove the QR clips from each helmet with the tool provided by the manufacturer. Helmets then were reassembled to allow each athletic trainer to attempt clip removal. Main Outcome Measure(s) The dependent variables were total left clips removed (TCR-L), total right clips removed (TCR-R), and total clips removed (TCR). Success rate of clip removal (SRCR) also was assessed. Results Percentages for TCR-L, TCR-R, and TCR were 100% (189 of 189), 96.30% (182 of 189), and 98.15% (371 of 378), respectively. A paired-samples t test revealed a difference between TCR-R and TCR-L (t188 = −2.689, P = .008, μd = 0.037, 95% confidence interval [CI] = −0.064, −0.010). The percentage for SRCR was 96.30% (n = 182), whereas SRCR percentages for trials 1, 2, and 3 were 95.24% (n = 60), 98.41% (n = 62), and 95.24% (n = 60), respectively, and did not represent a difference (F2,186 = 0.588, P = .56, 95% CI = 0.94, 0.99). Conclusions Our results indicated favorable and

[Seasonal variation patterns of NH4(+) -N/NO3(-) -N ratio and delta 15 NH4(+) value in rainwater in Yangtze River Delta].

Science.gov (United States)

Xie, Ying-Xin; Zhang, Shu-Li; Zhao, Xu; Xiong, Zheng-Qin; Xing, Guang-Xi

2008-09-01

By using a customized manual rainwater sampler made of polyvinyl chloride plastic, the molar ratio of NH4(+) -N/NO3(-) -N and the natural 15N abundance of NH4(+) (delta 15 NH4(+) in rainwater was monitored all year round from June 2003 to July 2005 at three observation sites (Changshu, Nanjing, and Hangzhou) in the Yangtze River Delta. The results indicated that at the three sites, the NH4(+) -N/NO3(-) -N ratio and the delta 15 NH4(+) value in rainwater had the similar seasonal variation trend, being more obvious in Changshu (rural monitoring type) site than in Nanjing (urban monitoring type) and Hangzhou (urban-rural monitoring type) sites. The NH4(+) -N/NO3(-) -N ratio peaked from early June to early August, declined gradually afterwards, and reached the bottom in winter; while the delta 15 NH4(+) value was negative from late June to mid-August, turned positive from late August to mid or late November, became negative again when winter dominated from December to March, but turned positive again in next May and negative again in next July. These seasonal variation patterns of NH4(+) -N/NO3(-) -N ratio and delta 15 NH4(+) value were found in relation to the application of chemical nitrogen fertilizers during different crop growth periods, and also, the alternation of seasons and the NH3 volatilization from other NH3 emission sources (including excrements of human and animals, nitrogen- polluted water bodies, and organic nitrogen sources, etc.), which could be taken as an indicator of defining the sources and form composition of NH4(+) in atmospheric wet deposition and the intensity of various terrestrial NH3 emission sources.

Extracting properties of N,N,N'N'-tetraalkyl-2 alkyl propane -1,3 diamides

International Nuclear Information System (INIS)

Nigond, L.

1992-01-01

N,N,N',N'-tetraalkyl -2 alkyl propane -1,3 diamides (RR'NCO) 2 CHR'' are investigated in the aim to separate actinides from nuclear wastes. N,N'-dimethyl N,N'-dibutyl tetradecylmalonamide (DMDBTDMA) was selected. This molecule can extract trivalent actinides in aliphatic diluents. Americium extraction is faster than iron extraction, hydrolytic degradation and solubility in aqueous phase are satisfactory. In non acidic media, diamides form aggregates, the size of which is function of diluent and diamide concentration. Extraction equilibria of HNO 3 , UO 2 2+ , Pu 4+ , Am 3+ and Fe 3+ are investigated.Four complexes are formed with nitric acid: L 2 HNO 3 , LHNO 3 , L 2 (HNO 3 ) 2 and L(HNO 3 ) 3 with L=DMDBTDMA. UO 2 2+ and Pu 4+ extraction takes place via the formation of neutral complexes: LUO 2 (NO 3 ) 2 , LPu(NO 3 ) 4 and L 2 Pu(NO 3 ) 4 for any nitric acid concentration. Am 3+ extraction takes place via the formation of LAm(NO 3 ) 3 and L 2 Am(NO 3 ) 3 for low nitric acid concentration and L x H y Am(NO 3 ) 3+y at higher acidity. Fe 3+ extraction involves anionic complexes L x HFe(NO 3 ) 4 for any acid concentration. In the presence of metallic cations, two kinds of interactions are observed: in the inner sphere of the metal diamide-metal ion complexation and in the outer sphere diamide-metallic complex interaction. The malonamide DMDBTDMA can be used to separate (III), (IV) and (VI) actinides from radioactive wastes

Biological nitrogen removal using soil columns for the reuse of reclaimed water: Performance and microbial community analysis.

Science.gov (United States)

Sun, Jiaji; Chen, Lei; Rene, Eldon R; Hu, Qian; Ma, Weifang; Shen, Zhenyao

2018-07-01

The main aim of this study was to remove nitrogen compounds from reclaimed water and reuse the water in semi-arid riverine lake systems. In order to assess the nitrogen removal efficiencies in different natural environments, laboratory scale column experiments were performed using sterilized soil (SS), silty clay (SC), soil with submerged plant (SSP) and biochar amendment soil (BCS). The initial concentration of NO 3 - -N and the flow rate was maintained constant at 15 mg L -1 and 0.6 ± 0.1 m d -1 , respectively. Among the tested columns, both SSP and BCS were able to achieve NO 3 - -N levels <0.2 mg L -1 in the treated reclaimed water. The results from bacterial community structure analysis, using 454 pyrosequencing of 16s rRNA genes, showed that the dominant denitrifier was Bacillus at the genera level. Copyright © 2018 Elsevier Ltd. All rights reserved.

Porous three-dimensional reduced graphene oxide merged with WO3 for efficient removal of radioactive strontium

Science.gov (United States)

Mu, Wanjun; Yu, Qianghong; Hu, rui; Li, Xingliang; Wei, Hongyuan; Jian, Yuan

2017-11-01

A simple hydrothermal method was used to prepare 3D nanostructured composite adsorbents of reduced graphene oxide (RGO) and WO3 (RGO/WO3). The analysis results suggest that it possesses a mesoporous 3D structure, in which WO3 nanorods are uniformly loaded on the surface of the RGO. Combining the benefits of GO and WO3, the composites exhibit a higher adsorption capacity for removing Sr2+ from aqueous solutions over a wide pH range (4-11). Adsorption isotherms show that the data fit the Langmuir isotherms well (R > 0.99), and the maximum adsorption capacity of 149.56 mg g-1 was achieved, much higher than that for GO, WO3 and other similar adsorbents. Sr2+ adsorption on RGO/WO3 reached equilibrium within 200 min. The fast adsorption and high adsorption rate of RGO/WO3 are mostly attributable to the plentiful adsorption sites provided by the dispersed WO3 nanoparticles on the RGO surface. Furthermore, the existence of Na+ ions has no obvious effect on the removal of Sr2+ ions by RGO/WO3, and RGO/WO3 adsorbent can be repeated at least 5 times without significant loss of adsorption capacity by adsorption-desorption experiment. Thus, RGO/WO3 shows the potential ability for removal of 90Sr from radioactive wastewater.

Removing Gaseous NH3 Using Biochar as an Adsorbent

Directory of Open Access Journals (Sweden)

Kyoung S. Ro

2015-09-01

Full Text Available Ammonia is a major fugitive gas emitted from livestock operations and fertilization production. This study tested the potential of various biochars in removing gaseous ammonia via adsorption processes. Gaseous ammonia adsorption capacities of various biochars made from wood shaving and chicken litter with different thermal conditions and activation techniques were determined using laboratory adsorption column tests. Ammonia adsorption capacities of non-activated biochars ranged from 0.15 to 5.09 mg·N/g, which were comparable to that of other commercial activated carbon and natural zeolite. There were no significant differences in ammonia adsorption capacities of steam activated and non-activated biochars even if the surface areas of the steam activated biochars were about two orders of magnitude greater than that of non-activated biochars. In contrast, phosphoric acid activation greatly increased the biochar ammonia adsorption capacity. This suggests that the surface area of biochar did not readily control gaseous NH3 adsorption. Ammonia adsorption capacities were more or less linearly increased with acidic oxygen surface groups of non-activated and steam-activated biochars. Phosphoric acid bound to the acid activated biochars is suspected to contribute to the exceptionally high ammonia adsorption capacity. The sorption capacities of virgin and water-washed biochar samples were not different, suggesting the potential to regenerate spent biochar simply with water instead of energy- and capital-intensive steam. The results of this study suggest that non-activated biochars can successfully replace commercial activated carbon in removing gaseous ammonia and the removal efficiency will greatly increase if the biochars are activated with phosphoric acid.

No-carrier-added (NCA) N-(3-( sup 18 F)fluoropropyl)-N-norbuprenorphine and N-(3-( sup 18 F)fluoropropyl)-N-nordiprenorphine -synthesis, anatomical distribution in mice and rats, and tomographic studies in a baboon

Energy Technology Data Exchange (ETDEWEB)

Bai, Lanqin; Teng, Renrui; Shiue, Chyngyann; Wolf, A P; Dewey, S L [Brookhaven National Lab., Upton, NY (USA); Holland, M J; Simon, E J [New York Univ., NY (USA). Medical Center

1990-01-01

N-(3-Fluoropropyl)-N-norbuprenorphine (3a) and N-(3-fluoropropyl)-N-nordiprenorphine (4a) were synthesized by N-alkylation of norbuprenorphine (1) and nordiprenorphine (2) with 1-bromo-3-fluoropropane. The corresponding no-carrier-added (NCA) N-(3-({sup 18}F)fluoropropyl)-N-norbuprenorphine (3b) and N-(3-({sup 18}F)fluoropropyl)-N-nordiprenorphine (4b) were synthesized by N-alkylation of 1 and 2 with NCA 1-({sup 18}F)fluoro-3-iodopropane. In vitro studies indicate that in the absence of sodium chloride, compounds 3a, 4a, N-propyl-N-norbuprenorphine (5), buprenorphine and diprenorphine are reasonably comparable in binding affinity for opioid receptors. In the presence of 100 mM sodium chloride, however, compounds 3a, 4a and 5, are clearly less potent than buprenorphine and diprenorphine. The anatomical distribution study of compound 3b in mice shows radioactivity accumulating in bone. Rat studies of both compounds 3b and 4b indicate the specific distribution of these two radioligands within certain cortical and subcortical regions of rat brain. However, the absolute uptake of compound 4b in rat brain was only half that of compound 3b. PET studies of 3b in a baboon revealed specific binding of compound 3b in striatum and cerebellum. At 1 h after injection, ratios of specific/non-specific binding of 3b in striatum and cerebellum of a baboon were 1.9 and 1.7 respectively. (author).

Hollow fiber contractors for simultaneous SO{sub x}/NO{sub x} removal

Energy Technology Data Exchange (ETDEWEB)

Bhown, A.S.; Pakala, N.R.; Riggs, T. [SRI International, Menlo Park, CA (United States)] [and others

1995-11-01

Control of SO{sub x} and NO{sub x} emissions from coal-fired utility and industrial boilers is a topic of growing national and international importance. Whereas a host of commercial and semicommercial processes exist, increasingly stringent emission standards mandate that processes be low cost, highly efficient, and, ideally, produce marketable byproducts. Although a wide range of site-specific economic factors dictate the best choice of SO{sub x} and NO{sub x} control, removal of SO{sub 2} by wet limestone scrubbing and removal of NO{sub x} by selective catalytic reduction (SCR) are regarded as the best commercialized technologies for this application. A typical wet limestone plant requires approximately $100 to $120 of capital investment per kilowatt of electric power generating capacity and has power and miscellaneous operating costs in the range of 5 to 6 mils per kilowatt hour (kWh). The SCR process requires approximately $70 to $100 of capital investment per kilowatt of electric power generating capacity. Its operating costs, including ammonia consumption, is in the range of 1.8 to 2.2 mils per kWh. These costs can add approximately 20% to the final cost of generated electricity, a significant burden on rate payers.

N2O, NO and CH4 exchange, and microbial N turnover over a Mediterranean pine forest soil

Directory of Open Access Journals (Sweden)

P. Rosenkranz

2006-01-01

Full Text Available Trace gas exchange of N2O, NO/NO2 and CH4 between soil and the atmosphere was measured in a typical Mediterranean pine (Pinus pinaster forest during two intensive field campaigns in spring and autumn 2003. Furthermore, gross and net turnover rates of N mineralization and nitrification as well as soil profiles of N2O and CH4 concentrations were determined. For both seasons a weak but significant N2O uptake from the atmosphere into the soil was observed. During the unusually dry and hot spring mean N2O uptake was −4.32 µg N m-2 h-1, whereas during the wet and mild autumn mean N2O uptake was −7.85 µg N m-2 h-1. The observed N2O uptake into the soil was linked to the very low availability of inorganic nitrogen at the study site. Organic layer gross N mineralization decreased from 5.06 mg N kg-1 SDW d-1 in springtime to 2.68 mg N kg-1 SDW d-1 in autumn. Mean NO emission rates were significantly higher in springtime (9.94 µg N m-2 h-1 than in autumn (1.43 µg N m-2 h-1. A significant positive correlation between NO emission rates and gross N mineralization as well as nitrification rates was found. The negative correlation between NO emissions and soil moisture was explained with a stimulation of aerobic NO uptake under N limiting conditions. Since NO2 deposition was continuously higher than NO emission rates the examined forest soil functioned as a net NOx sink. Observed mean net CH4 uptake rates were in spring significantly higher (−73.34 µg C m-2 h-1 than in autumn (−59.67 µg C m-2 h-1. Changes in CH4 uptake rates were strongly negatively correlated with changes in soil moisture. The N2O and CH4 concentrations in different soil depths revealed the organic layer and the upper 0.1 m of mineral soil as the most important soil horizons for N2O and CH4 consumption.

Thermochemical characteristics of La n+1Ni nO3n+1 oxides

International Nuclear Information System (INIS)

Bannikov, D.O.; Safronov, A.P.; Cherepanov, V.A.

2006-01-01

Lanthanum nickelates: La 2 NiO 4+δ , La 3 Ni 2 O 7-δ , La 4 Ni 3 O 10-δ and LaNiO 3-δ the members of Ruddlesden-Popper series La n+1 Ni n O 3n+1 were prepared using citrate route. Dissolution enthalpies of complex oxides as well as a number of subsidiary substances were measured by means of Calvet calorimeter in 1 M solution of hydrochloric acid at 25 deg. C. The dissolution scheme of complex oxides in hydrochloric acid was proposed and enthalpies of formation of the complex oxides from binary oxides were calculated considering oxygen nonstoichiometry of these substances. Enthalpies of step-by-step oxidation were evaluated. Partial enthalpy contribution of LaO layers was calculated endothermic equals to 30.9 J/mol while partial enthalpy contribution of perovskite LaNiO 3 layers was negative equals to -97.0 J/mol. Enthalpy of formation of any complex oxide of Ruddlesden-Popper series fits very well to the linear regression based on these values

Method to remove NO/sub x/ from combustion exhaust gases. [German patent

Energy Technology Data Exchange (ETDEWEB)

Mizuno, M.; Iwata, T.

1975-11-13

The invention to remove NO/sub x/ from combustion exhaust gases is proposed by means of an example and a drawing. The exhaust gas is washed with an aqueous 30% ammonium sulfite solution (pH = 6.1 - 6-6.5, d = 50 to 55/sup 0/C) and then reduced with waste ammonia in the catalyst bed at 200 to 450/sup 0/C. The total SO/sub 2/ is removed in the prewash procedure and the NH/sub 3/ required for the reduction is transferred from the washing solution to the exhaust gas. The washing solution is regenerated with coke gas containing NH/sub 3/ (150 to 500 ppM NH/sub 3/). Iron ore, tinder, hammer scale, iron-contained dust, copper oxide, chromium oxide, cobalt oxide, and vanadium oxide are suitable as catalyst for the reduction process.

Use of bioreactor landfill for nitrogen removal to enhance methane production through ex situ simultaneous nitrification-denitrification and in situ denitrification.

Science.gov (United States)

Sun, Xiaojie; Zhang, Hongxia; Cheng, Zhaowen

2017-08-01

High concentrations of nitrate-nitrogen (NO 3 - -N) derived from ex situ nitrification phase can inhibit methane production during ex situ nitrification and in situ denitrification bioreactor landfill. A combined process comprised of ex situ simultaneous nitrification-denitrification (SND) in an aged refuse bioreactor (ARB) and in situ denitrification in a fresh refuse bioreactor (FRB) was conducted to reduce the negative effect of high concentrationsof NO 3 - -N. Ex situ SND can be achieved because NO 3 - -N concentration can be reduced and the removal rate of ammonium-nitrogen (NH 4 + -N) remains largely unchanged when the ventilation rate of ARB-A2 is controlled. The average NO 3 - -N concentrations of effluent were 470mg/L in ex situ nitrification ARB-A1 and 186mg/L in ex situ SND ARB-A2. The average NH 4 + -N removal rates of ARB-A1 and ARB-A2 were 98% and 94%, respectively. Based on the experimental data from week 4 to week 30, it is predicted that NH 4 + -N concentration in FRB-F1 of the ex situ nitrification and in situ denitrification process would reach 25mg/L after 63weeks, and about 40weeks for the FRB-F2 of ex situ SND and in situ denitrification process . Ex situ SND and in situ denitrification process can improve themethane production of FRB-F2. The lag phase time of methane production for the FRB-F2 was 11weeks. This phase was significantly shorter than the 15-week phases of FRB-F1 in ex situ nitrification and in situ denitrification process. A seven-week stabilizationphase was required to increase methane content from 5% to 50% for FRB-F2. Methane content in FRB-F1 did not reach 50% but reached the 45% peak after 20weeks. Copyright © 2017 Elsevier Ltd. All rights reserved.

Simultaneous removal of NO and SO2 with hexamminecobalt(II) solution coupled with the hexamminecobalt(II) regeneration catalyzed by activated carbon

International Nuclear Information System (INIS)

Long, Xiang-Li; Xin, Zhi-Ling; Wang, Hong-Xin; Xiao, Wen-De; Yuan, Wei-Kang

2004-01-01

The wet ammonia desulfurization process can be retrofitted for combined removal of SO 2 and NO from the flue gases by adding soluble cobalt(II) salt into the aqueous ammonia solution. Activated carbon is used to catalyze the reduction of hexamminecobalt(III) to hexamminecobalt(II) to maintain the capability of removing NO of the hexamminecobalt solution. The effects of temperature, pH, activated carbon particle size, and superficial liquid flow velocity on hexamminecobalt(III) conversion have been investigated. An apparent activation energy is obtained. According to the experimental results, the catalytic reduction reaction rate increases with temperature. The batch reactor experiments show that the best pH range lies in between 3.5 and 6.5. In a fixed-bed reactor, superficial liquid flow velocity obviously affects the reaction and a high yield of cobalt(II) is obtained at a pH value lower than 9.0. The experiments manifest that the hexamminecobalt solution coupled with catalytic regeneration of hexamminecobalt(II) can maintain a high nitric oxide removal efficiency during a period of time

Report on Influence of Physical and Biological Soil Processes on NO3- Fertilizer

International Nuclear Information System (INIS)

Rolston, D.E.

1981-01-01

Denitrification of nitrate (NO 3 - ) fertilizer was simulated using a mathematical model. The rate of denitrification was considered to be a function of NO 3 - concentration, available carbon (C) concentration, degree of soil-water saturation, and temperature. Available C concentrations were calculated from initial amounts of soil C and additions of plant residues or animal manure. The consumption of added C in the soil system was assumed to occur in 2 or 3 stages with different rate constants for each stage and C source. A Q 10 value of 2 was used in correcting denitrification rate constants and C consumption constants at two temperatures. Model simulations for denitrification were compared with measured N 2 and N 2 O gas fluxes during nitrate leaching in field plots of Yolo soil at different soil-water content, C additions, soil temperature, and irrigation frequencies

Nitrate removal and microbial analysis by combined micro-electrolysis and autotrophic denitrification.

Science.gov (United States)

Xing, Wei; Li, Desheng; Li, Jinlong; Hu, Qianyi; Deng, Shihai

2016-07-01

A process combining micro-electrolysis and autotrophic denitrification (CEAD) with iron-carbon micro-electrolysis carriers was developed for nitrate removal. The process was performed using organic-free influent with a NO3(-)-N concentration of 40.0±3.0mg/L and provided an average nitrate removal efficiency of 95% in stable stages. The total nitrogen removal efficiency reached 75%, with 21% of NO3(-)-N converted into NH4(+)-N. The corresponding hydraulic retention time was 8-10h, and the optimal pH ranged from 8.5 to 9.5. Microbial analysis with high-throughput sequencing revealed that dominant microorganisms in the reactor belonged to the classes of β-, γ-, and α-Proteobacteria. The abundance of the genera Thermomonas significantly increased during the operation, comprising 21.4% and 24.1% in sludge attached to the carriers in the middle and at the bottom of the reactor, respectively. The developed CEAD achieved efficient nitrate removal from water without organics, which is suitable for practical application. Copyright © 2016. Published by Elsevier Ltd.

Effective Biological Nitrogen Removal Treatment Processes for Domestic Wastewaters with Low C/N Ratios: A Review

DEFF Research Database (Denmark)

Sun, Sheng-Peng; Pellicer i Nàcher, Carles; Merkey, Brian

2010-01-01

with high efficiency and relative low costs. However, the removal of nitrogen from domestic wastewater with a low carbon/nitrogen (C/N) ratio can often be limited in municipal wastewater plants (WWTPs) because organic carbon is a limiting factor for denitrification. The present work reviews innovative....... They can effectively be used for nitrogen removal from low C/N domestic wastewater without external carbon addition. In addition, conventional and alternative carbon sources for enhanced biological nitrogen removal were also reviewed. We conclude that alternative carbon sources such as wine distillery...... at large scale for nitrogen removal from low C/N domestic wastewater, (2) further method logic are explored to introduce the Anammox pathway into domestic wastewater treatment, and (3) alternative carbon sources are explored and optimized for supporting the denitrification. With these efforts, cost...

Dynamics of N-NH4 +, N-NO3 -, and total soil nitrogen in paddy field with azolla and biochar

Science.gov (United States)

Dewi, W. S.; Wahyuningsih, G. I.; Syamsiyah, J.; Mujiyo

2018-03-01

Nitrogen (N) is one of macronutrients which is dynamic in the soil and becomes constraint factor for rice crops. The addition of nitrogen fertilizers and its absorption in paddy field causes the dynamics of nitrogen, thus declines of N absorption efficiency. The aim of this research is to know influence Azolla, biochar and different varieties application on N-NH4 +, N-NO3 -, and total soil N in paddy field. This research was conducted in a screen house located in Jumantono Laboratory, Faculty of Agriculture, Universitas Sebelas Maret (UNS) with altitude 170 m asl from April to June 2016. Treatment factors that were examined consisted of azolla (0 and 10 tons/ha), biochar (0 and 2 tons/ha), and rice varieties (Cisadane, Memberamo, Ciherang, IR64). The results of this research showed that there was no interaction between azolla, biochar and varieties. Nevertheless, azolla treatment with dose of 10 tons/ha increased soil NH4 + content (41 days after planting, DAP) by 13.4% but tend to decrease at 70 and 90 DAP. Biochar treatment with dose of 2 ton/ha increases NO3 - soil content (70 DAP) by 1.7% but decreases total N soil by 5.8% (41 DAP) and 4.7% (90 DAP). Different rice varieties generated different soil NH4 + content (41 DAP) and rice root volume. Cisadane variety can increase soil NH4 + content (41 DAP) by 52.08% and root volume by 51.80% (90 DAP) compared with Ciherang variety. Organic rice field management with azolla and biochar affects the availability of N in the soil and increase N absorption efficiency through its role in increasing rice root volume.

Kinetics and branching ratios of the reactions NH2+NO2->N2O+H2O and NH2+NO2->H2NO+NO studied by pulse radiolysis combined with time-resolved infrared diode laser spectroscopy

DEFF Research Database (Denmark)

Meunier, H.; Pagsberg, Palle Bjørn; Sillesen, A.

1996-01-01

studied by monitoring the decay of NH2 and the simultaneous formation of N2O and NO by time-resolved infrared diode laser spectroscopy. The decay rate of NH2 was studied as a function of NO2 concentration to obtain an overall rate constant k(NH2 + NO2) = (1.35 +/- 0.15) X 10(-11) molecule(-1) cm(3) s(-1...

Different fates of deposited NH4+ and NO3- in a temperate forest in northeast China: a 15 N tracer study.

Science.gov (United States)

Liu, Jun; Peng, Bo; Xia, Zongwei; Sun, Jianfei; Gao, Decai; Dai, Weiwei; Jiang, Ping; Bai, Edith

2017-06-01

Increasing atmospheric reactive nitrogen (N) deposition due to human activities could change N cycling in terrestrial ecosystems. However, the differences between the fates of deposited NH4+ and NO3- are still not fully understood. Here, we investigated the fates of deposited NH4+ and NO3-, respectively, via the application of 15 NH 4 NO 3 and NH 4 15 NO 3 in a temperate forest ecosystem. Results showed that at 410 days after tracer application, most 15NH4+ was immobilized in litter layer (50 ± 2%), while a considerable amount of 15NO3- penetrated into 0-5 cm mineral soil (42 ± 2%), indicating that litter layer and 0-5 cm mineral soil were the major N sinks of NH4+ and NO3-, respectively. Broad-leaved trees assimilated more 15 N under NH 4 15 NO 3 treatment compared to under 15 NH 4 NO 3 treatment, indicating their preference for NO3--N. At 410 days after tracer application, 16 ± 4% added 15 N was found in aboveground biomass under 15NO3- treatment, which was twice more than that under 15NH4+ treatment (6 ± 1%). At the same time, approximately 80% added 15 N was recovered in soil and plants under both treatments, which suggested that this forest had high potential for retention of deposited N. These results provided evidence that there were great differences between the fates of deposited NH4+ and NO3-, which could help us better understand the mechanisms and capability of forest ecosystems as a sink of reactive nitrogen. © 2016 John Wiley & Sons Ltd.

Epidemiological Data and Survival Rate of Removable Partial Dentures

Science.gov (United States)

Moreno, Amália; Haddad, Marcela Filié; Rocha, Eduardo Passos; Assunção, Wirley Gonçalves; Filho, Humberto Gennari; Santos, Emerson Gomes Dos; Sonego, Mariana Vilela; Santos, Daniela Micheline Dos

2016-01-01

Introduction The use of removable partial denture (RPD) is considered as low-cost and common treatment option to rehabilitate edentulous areas. Aim This study aimed to investigate the epidemiological data of patients rehabilitated with removable partial denture (RPD) in order to assess treatment survival rate and failures. Materials and Methods Epidemiological data and medical records of patients treated with RPD between 2007 and 2012 at the RPD discipline of a Brazilian University (Aracatuba Dental School- UNESP) were evaluated as well as dental records of patients who underwent RPD treatments (fabrication or repairs) between 2000 and 2010. Factors such as gender, age, presence of systemic disease, main complaint, edentulous arch, period and cause of denture replacement and the prosthesis characteristics were recorded. The chi-square test was used to assess the differences between the variables and the Kaplan Meyer to assess the survival of the RPDs evaluated. Results A total of 324 maxillary RPD and 432 mandibular RPD were fabricated. Most of the patients were women aging 41 to 60-year-old. The number of mandibular RPD Kennedy class I (26%) was statistically higher for the maxillary arch (p<.05). There was no association between main complaint to gender or the presence of systemic disease. The lingual plate was the most common major connector used in the mandible (32%). The main reason for altering the design of replaced RPDs were changes during treatment plan. Conclusion The number of patients who require RPD is large; most of RPDs are Kennedy Class I. A good treatment plan is very important for achieving a positive treatment outcome, and it is strictly related to the survival rate. PMID:27437367

Mathematical Modeling of Nitrous Oxide Production during Denitrifying Phosphorus Removal Process.

Science.gov (United States)

Liu, Yiwen; Peng, Lai; Chen, Xueming; Ni, Bing-Jie

2015-07-21

A denitrifying phosphorus removal process undergoes frequent alternating anaerobic/anoxic conditions to achieve phosphate release and uptake, during which microbial internal storage polymers (e.g., Polyhydroxyalkanoate (PHA)) could be produced and consumed dynamically. The PHA turnovers play important roles in nitrous oxide (N2O) accumulation during the denitrifying phosphorus removal process. In this work, a mathematical model is developed to describe N2O dynamics and the key role of PHA consumption on N2O accumulation during the denitrifying phosphorus removal process for the first time. In this model, the four-step anoxic storage of polyphosphate and four-step anoxic growth on PHA using nitrate, nitrite, nitric oxide (NO), and N2O consecutively by denitrifying polyphosphate accumulating organisms (DPAOs) are taken into account for describing all potential N2O accumulation steps in the denitrifying phosphorus removal process. The developed model is successfully applied to reproduce experimental data on N2O production obtained from four independent denitrifying phosphorus removal study reports with different experimental conditions. The model satisfactorily describes the N2O accumulation, nitrogen reduction, phosphate release and uptake, and PHA dynamics for all systems, suggesting the validity and applicability of the model. The results indicated a substantial role of PHA consumption in N2O accumulation due to the relatively low N2O reduction rate by using PHA during denitrifying phosphorus removal.

Influence of organic carbon and nitrate loading on partitioning between dissimilatory nitrate reduction to ammonium (DNRA) and N2 production

Science.gov (United States)

Hardison, Amber K.; Algar, Christopher K.; Giblin, Anne E.; Rich, Jeremy J.

2015-09-01

Biologically available nitrogen is removed from ecosystems through the microbial processes of anaerobic ammonium oxidation (anammox) or denitrification, while dissimilatory nitrate reduction to ammonium (DNRA) retains it. A mechanistic understanding of controls on partitioning among these pathways is currently lacking. The objective of this study was to conduct a manipulative experiment to determine the influence of organic C and NO3- loading on partitioning. Sediment was collected from a location on the southern New England shelf (78 m water depth) and sieved. Half of the sediment was mixed with freeze-dried phytoplankton and the other half was not. Sediment was then spread into 1.5 mm, "thin discs" closed at the bottom and placed in large aquarium tanks with filtered, N2/CO2 sparged seawater to maintain O2 limited conditions. Half of the discs received high NO3- loading, while the other half received low NO3- loading, resulting in a multifactorial design with four treatments: no C addition, low NO3- (-C-N); C addition, low NO3- (+C-N); no C addition, high NO3- (-C+N); and C addition, high NO3- (+C+N). Sediment discs were incubated in the tanks for 7 weeks, during which time inorganic N (NH4+, NO3-, and NO2-) was monitored, and sediment discs were periodically removed from the tanks to conduct 15N isotope labeling experiments in vials to measure potential rates of anammox, denitrification, and DNRA. Temporal dynamics of inorganic N concentrations in the tanks were indicative of anoxic N metabolism, with strong response of the build up or consumption of the intermediate NO2-, depending on treatments. Vial incubation experiments with added 15NO2- + 14NH4+ indicated significant denitrification and DNRA activity in sediment thin discs, but incubations with added 15NH4+ + 14NO2- indicated anammox was not at all significant. Inorganic N concentrations in the tanks were fit to a reactive transport model assuming different N transformations. Organic C decomposition rates

[Characteristics of nitrogen and phosphorus removal and control of membrane fouling in MBR and SMBR].

Science.gov (United States)

Guo, Xiao-Ma; Zhao, Yan; Wang, Kai-Yan; Zhao Yang-Guo

2015-03-01

To improve the efficiency and running stability of wastewater advanced treatment, a sequencing membrane bioreactor (SMBR) and a traditional membrane bioreactor (MBR) were used to investigate the characteristics of nitrogen and phosphorus removal, and the effect of anoxic time on treatment systems and membrane fouling. Simultaneously, molecular biology techniques were applied to analyze the composition of microbial community and the structure of suspended sludge. The results showed that SMBR had higher efficiency in removing TN than MBR, which indicated that intermittent aeration could enhance the ability of nitrogen removal. SMBR and MBR had a similar removal efficiency of NH4(+)-N, TP, COD, and turbidity with the removal rates of 94%, 78%, 80%, and 97%, respectively. Extension of SMBR anoxic time had no effect on COD, NH4(+) -N removal but decreased TN and TP removal rate, dropping from 61% and 74% to 46% and 52%, respectively. Intermittent aeration and powder activated carbon (PAC) could both mitigate membrane fouling. The analysis on microbial community indicated that there was no difference in the composition and structure of microbial community between SMBR and MBR. Nitrospira and Dechloromonas were both highly abundant functional groups, which provided the basis for highly efficient control of bioreactors.

The effect of poly-β-hydroxyalkanoates degradation rate on nitrous oxide production in a denitrifying phosphorus removal system.

Science.gov (United States)

Wei, Yan; Wang, Shuying; Ma, Bin; Li, Xiyao; Yuan, Zhiguo; He, Yuelan; Peng, Yongzhen

2014-10-01

Poly-β-hydroxyalkanoates (PHAs) and free nitrous acid (FNA) have been revealed as significant factors causing nitrous oxide (N2O) production in denitrifying phosphorus removal systems. In this study, the effect of PHA degradation rate on N2O production was studied at low FNA levels. N2O production always maintained at approximately 40% of the amount of nitrite reduced independent of the PHA degradation rate. The electrons distributed to nitrite reduction were 1.6 times that to N2O reduction. This indicated that electron competition between these two steps was not affected by the PHA degradation rate. Continuous feed of nitrate was proposed, and demonstrated to reduce N2O accumulation by 75%. While being kept low, a possible compounding effect of a low-level FNA could not be ruled out. The sludge used likely contained both polyphosphate- and glycogen-accumulating organisms, and the results could not be simply attributed to either group of organisms. Copyright © 2014 Elsevier Ltd. All rights reserved.

Poly[(6-carboxypicolinato-κ3O2,N,O6(μ3-pyridine-2,6-dicarboxylato-κ5O2,N,O6:O2′:O6′dysprosium(III

Directory of Open Access Journals (Sweden)

Xu Li

2009-11-01

Full Text Available In the title complex, [Dy(C7H3NO4(C7H4NO4]n, one of the ligands is fully deprotonated while the second has lost only one H atom. Each DyIII ion is coordinated by six O atoms and two N atoms from two pyridine-2,6-dicarboxylate and two 6-carboxypicolinate ligands, displaying a bicapped trigonal-prismatic geometry. The average Dy—O bond distance is 2.40 Å, some 0.1Å longer than the corresponding Ho—O distance in the isotypic holmium complex. Adjacent DyIII ions are linked by the pyridine-2,6-dicarboxylate ligands, forming a layer in (100. These layers are further connected by π–π stacking interactions between neighboring pyridyl rings [centroid–centroid distance = 3.827 (3 Å] and C—H...O hydrogen-bonding interactions, assembling a three-dimensional supramolecular network. Within each layer, there are other π–π stacking interactions between neighboring pyridyl rings [centroid–centroid distance = 3.501 (2 Å] and O—H...O and C—H...O hydrogen-bonding interactions, which further stabilize the structure.

Characteristics of NH4+ and NO3− fluxes in tea (Camellia sinensis) roots measured by scanning ion-selective electrode technique

Science.gov (United States)

Ruan, Li; Wei, Kang; Wang, Liyuan; Cheng, Hao; Zhang, Fen; Wu, Liyun; Bai, Peixian; Zhang, Chengcai

2016-01-01

As a vital beverage crop, tea has been extensively planted in tropical and subtropical regions. Nitrogen (N) levels and forms are closely related to tea quality. Based on different N levels and forms, we studied changes in NO3− and NH4+ fluxes in tea roots utilizing scanning ion-selective electrode technique. Our results showed that under both single and mixed N forms, influx rates of NO3− were much lower than those of NH4+, suggesting a preference for NH4+ in tea. With the increase in N concentration, the influx rate of NO3− increased more than that of NH4+. The NH4+ influx rates in a solution without NO3− were much higher than those in a solution with NO3−, while the NO3− influx rates in a solution without NH4+ were much lower than those in a solution with NH4+. We concluded that (1) tea roots showed a preference for NH4+, (2) presence of NO3− had a negative effect on NH4+ influx, and (3) NH4+ had a positive effect on NO3− influx. Our findings not only may help advance hydroponic tea experiments but also may be used to develop efficient fertilization protocols for soil-grown tea in the future. PMID:27918495

Effect of periodontal ligament removal with gauze prior to delayed replantation in rabbit incisors on rate of replacement resorption.

Science.gov (United States)

Maslamani, Manal; Joseph, Bobby; Gabato, Severino; Andersson, Lars

2018-03-23

Delayed (dry storage > 60 minutes) replantation results in ankylosis and replacement resorption. It has been suggested to remove the non-viable periodontal ligament before replantation to possibly reduce the rate of replacement resorption. However there has been no study on the rate of replacement resorption after such measures. The aim of this study was to investigate if there was any difference in the rate of replacement resorption by either removing the periodontal ligament (PDL) with gauze or not removing PDL in teeth subjected to delayed replantation followed by healing for 2 or 6 weeks. Maxillary central incisors were extracted in 8 rabbits. In the right central incisors, the necrotic PDL was removed by dry gauze over the root surface. In the left eight extracted teeth PDL was left on the root surface. All extracted teeth were left to dry for 60 minutes. Extra-oral root canal treatment was performed before replantation. The rabbits were sacrificed after 2 weeks and 6 weeks respectively. Histologic processing and evaluation was done. In the 2 weeks group, all teeth showed ankylosis. The cementum was intact, and fusion of the bone and root was generally seen without resorption of the root, whereas in the 6 weeks group regardless of whether PDL had been kept or not, ankylosis and osseous replacement of the dentin was seen. There was no evidence of inflammatory infiltrate in the sections examined. Removal of PDL prior to delayed replantation may result in some initial protection of the cementum during the first few weeks. However, over longer times there seems to be neither protection of the dentin from ankylosis and osseous replacement, nor any influence on the rate of replacement resorption. © 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Investigations of the mechanism of vitamin E removal from blood and the effect of NO2 on the pulmonary uptake of vitamin E

International Nuclear Information System (INIS)

Gardner, H.K.

1987-01-01

To examine the effect of NO 2 on vitamin E uptake by lung, we first investigated the mechanism of removal of vitamin E from blood. To accomplish this, a method for labeling serum with tritiated vitamin E was developed. Two other lipids, whose uptake is better understood, were also studied, and compared with vitamin E. Tritiated triacylglycerol was used to monitor lipoprotein lipase-mediated uptake, while tritiated cholesterol was used to monitor LDL receptor-mediated uptake. Blood curves derived from untreated, adult, male, Long-Evans rats indicated that all three lipids were removed biexponentially. The half-life for the Rapid component was 2.5-3.7 minutes for all lipids. The slower curve had half-lives of 42.3 minutes for triacylglycerol, 990.0 minutes for cholesterol, and 288.8 minutes for vitamin E. Biological screening of labeled serum demonstrated that the faster process was not simply the removal of lipoproteins damaged by the labeling process. Hepatectomy affected the rate of neither triacylglycerol nor cholesterol removal, but did slow vitamin E uptake, suggesting a distinct role for liver in vitamin E extraction

105-N Basin sediment removal subcontract acquisition strategy plan

International Nuclear Information System (INIS)

Wilsey, D.J.

1997-01-01

The 105-N Basin Sediment Removal Subcontract Acquisition Strategy Plan provides a detailed set of actions to specify and procure services and equipment for removal of approximately 400 ft 3 (wet) of radioactive sediment. The plan outlines a cost-effective approach to remove this sediment safely and within an aggressive schedule. This 105-N Basin Sediment Removal Strategy Plan includes the following key elements: a current vendor survey of capabilities and interest in this type of work, confirming that qualified, competitive sources are available, and in the time frame required; a systematic review of the various options for sediment disposal in enough detail to exhaustively uncover pros and cons of each approach; use of a workshop approach to assess different ways to accomplish the work and ensure the disposal options considered are cost and schedule effective; integration of the complicated sampling and characterization process, which is essential to successful execution of the procurement scheme; review of the various subcontracting options to maximize the use of existing technology, existing equipment, and specialized expertise; detailed early planning and strategizing for early identification of problems that can be solved early before they become restraints or potential added costs; tailored design schedule to cover three alternate approaches so that sample characterization will not delay engineering preparation for disposal; support required from various organizations onsite as well as subcontractors, well in advance of the need for that support, improving availability of the proper personnel to support schedule and cost objectives; and provides the possible opportunity to process the sediment in the valve pit and pump pit through this same subcontractor's process

Addition and spin exchange rate constants by longitudinal field μSR: the Mu + NO reaction

International Nuclear Information System (INIS)

Senba, Masayoshi; Gonzalez, A.C.; Kempton, J.R.; Arseneau, D.J.; Pan, J.J.; Tempelmann, A.; Fleming, D.G.

1991-01-01

The addition reaction Mu + NO + M → MuNO + M and the spin exchange reaction Mu(↑) + NO(↓)→Mu(↓)+NO(↑) have been measured by longitudinal field μSR at room temperature in the presence of up to 58 atm of N 2 as inert collider. The pressure dependence of the longitudinal relaxation rate due to the addition reaction (λ c ) demonstrates that the system is still in the low pressure regime in this pressure range. The corresponding termolecular rate constant has been determined as k 0.Mu =(1.10±0.25)x10 -32 cm 6 molecules -2 s -1 , almost 4 times smaller than the corresponding H atom reaction k 0,H =3.90x10 -32 cm 6 molecules -2 s -1 . The average value of the spin exchange rate constants in the 2.5-58 atm pressure range, k SE = (3.16±0.06)x10 -10 cm 3 molecule -1 s -1 , is in good agreement with previous values obtained by transverse field μSR. (orig.)

The role of healed N-vacancy defective BC2N sheet and nanotube by NO molecule in oxidation of NO and CO gas molecules

Science.gov (United States)

Nematollahi, Parisa; Esrafili, Mehdi D.; Neyts, Erik C.

2018-06-01

In this study, the healing of N-vacancy boron carbonitride nanosheet (NV-BC2NNS) and nanotube (NV-BC2NNT) by NO molecule is studied by means of density functional theory calculations. Two different N-vacancies are considered in each of these structures in which the vacancy site is surrounded by either three B-atoms (NB) or by two B- and one C-atom (NBC). By means of the healed BC2NNS and BC2NNT as a support, the removal of two toxic gas molecules (NO and CO) are applicable. It should be noted that the obtained energy barriers of both healing and oxidizing processes are significantly lower than those of graphene, carbon nanotubes or boron nitride nanostructures. Also, at the end of the oxidation process, the pure BC2NNS or BC2NNT is obtained without any additional defects. Therefore, by using this method, we can considerably purify the defective BC2NNS/BC2NNT. Moreover, according to the thermochemistry calculations we can further confirm that the healing process of the NV-BC2NNS and NV-BC2NNT by NO are feasible at room temperature. So, we can claim that this study could be very helpful in both purifying the defective BC2NNS/BC2NNT while in the same effort removing toxic NO and CO gases.

NO3-/NH4+ proportions affect cadmium bioaccumulation and tolerance of tomato.

Science.gov (United States)

Nogueirol, Roberta Corrêa; Monteiro, Francisco Antonio; de Souza Junior, João Cardoso; Azevedo, Ricardo Antunes

2018-05-01

With the growth of the world population, cadmium (Cd) concentration in the environment has increased considerably as a result of human activities such as foundry, battery disposal, mining, application of fertilizers containing toxic elements as impurities, and disposal of metal-containing waste. Higher plants uptake N as ammonium (NH 4 + ), nitrate (NO 3 - ), and many other water-soluble compounds such as urea and amino acids, and nourishing plants with N, providing part of it as NH 4 + , is an interesting alternative to the supply of this nutrient in the exclusive form of NO 3 - under Cd toxicity. The objective was to evaluate the influence of NO 3 - /NH 4 + proportions on the development and tolerance of tomato plants grown under the presence of Cd in the culture medium. The experiment was conducted in a completely randomized block design in a 3 × 3 factorial arrangement consisting of three Cd rates (0, 50, and 100 μmol L -1 ) and three NO 3 - /NH 4 + proportions (100/0, 70/30, and 50/50) in the nutrient solution. To this end, we quantified the responses of the antioxidant enzymatic system and productive and functional changes in Solanum lycopersicum var. esculentum (Calabash Rouge). Shoot biomass production decreased with the maximum Cd rate (100 μmol L -1 ) tested in the growth medium, whereas the NO 3 - /NH 4 + proportions and other Cd rates did not significantly influence this variable. The lowest SPAD values were observed at the 100/0 NO 3 - /NH 4 + proportion and in plants exposed to Cd. The largest accumulation of the metal occurred in the shoots at the NO 3 - /NH 4 + proportion of 70/30 and at 100 μmol L -1 Cd and in the roots at 100/0 NO 3 - /NH 4 + and with 50 and 100 μmol L -1 Cd. The concentration and accumulation of NO 3 - were highest at the NO 3 - /NH 4 + proportion of 100/0 in the shoots and at 50/50 NO 3 - /NH 4 + in the roots, whereas for NH 4 + , values were higher as the proportion of N supplied in the form of NH 4 + was

Nitrate as an Oxidant in the Cathode Chamber of a Microbial Fuel Cell for Both Power Generation and Nutrient Removal Purposes

DEFF Research Database (Denmark)

Fang, Cheng; Min, Booki; Angelidaki, Irini

2011-01-01

with the operation without catalyst. Nitrate was reduced to nitrite and ammonia in the liquid phase at a ratio of 0.6% and 51.8% of the total nitrate amount. These results suggest that nitrate can be successfully used as an oxidant for power generation without aeration and also nitrate removal from water in MFC......Nitrate ions were used as the oxidant in the cathode chamber of a microbial fuel cell (MFC) to generate electricity from organic compounds with simultaneous nitrate removal. The MFC using nitrate as oxidant could generate a voltage of 111 mV (1,000 Ω) with a plain carbon cathode. The maximum power...... density achieved was 7.2 mW m−2 with a 470 Ω resistor. Nitrate was reduced from an initial concentration of 49 to 25 mg (NO3−−N) L−1 during 42-day operation. The daily removal rate was 0.57 mg (NO3−–N) L−1 day−1 with a voltage generation of 96 mV. In the presence of Pt catalyst dispersed on cathode...

[Effect of Different Purple Parent Rock on Removal Rates of Nitrogen, Phosphorus and Organics in Landscape Water].

Science.gov (United States)

Huang, Xue-jiao; Liu, Xiao-chen; Li, Zhen-lun; Shi, Wen-hao; Yang, Shan

2015-05-01

In order to understand the impacts of physicochemical properties of purple parent rock on the removal rates of nitrogen, phosphorus and organics in landscape water systems, four types of purple parent rocks including Peng-lai-zhen Formation (S1) , Sha-xi-miao Formation (S2) , Fei-xian-guan Formation (S3) and Sui-ning Formation (S4) , which distribute widely in Chongqing, were selected and autoclaved, and added to unsterile landscape water collected from Chong-de Lake in Southwest University, and the landscape water only was used as control. And several indicators such as total nitrogen and phosphorus and so on of every disposal were investigated periodically. The results indicated that: (1) The highest removal rates of total nitrogen, total phosphorus and Ammonia nitrogen were observed in Sl, which were 45.1%, 62.3% and 90%, respectively; the highest removal rate of COD was 94.5% in S4; the ammonia nitrogen content in the purple parent rocks was not obviously changed before and after the experiments, which indicated that the adsorption of ammonia nitrogen on purple parent rock surface was not the main reason for the decrease of ammonia nitrogen in water. (2) Arsenate had inhibitory effect on the sulfate-reducing bacteria, while copper and magnesium had promoting effect on gram-negative bacteria. (3) The microbial diversity was positively correlated to total nitrogen in water. (4) Based on the PCA analyses of microbial community structure and environmental factors, the mineral elements released from parent rock affected the structure and composition of microbial community in the test water, and then influenced the removal rates of nitrogen, phosphorus and organics in water systems.

Atmospheric cycles of nitrogen oxides and ammonia. [source strengths and destruction rates

Science.gov (United States)

Bottger, A.; Ehhalt, D. H.; Gravenhorst, G.

1981-01-01

The atmospheric cycles of nitrogenous trace compounds for the Northern and Southern Hemispheres are discussed. Source strengths and destruction rates for the nitrogen oxides: NO, NO2 and HNO3 -(NOX) and ammonia (NH3) are given as a function of latitude over continents and oceans. The global amounts of NOX-N and NH3-N produced annually in the period 1950 to 1975 (34 + 5 x one trillion g NOx-N/yr and 29 + or - 6 x one trillion g NH3-N/yr) are much less than previously assumed. Globally, natural and anthropogenic emissions are of similar magnitude. The NOx emission from anthropogenic sources is 1.5 times that from natural processes in the Northern Hemisphere, whereas in the Southern Hemisphere, it is a factor of 3 or 4 less. More than 80% of atmospheric ammonia seems to be derived from excrements of domestic animals, mostly by bulk deposition: 24 + or - 9 x one trillion g NO3 -N/yr and 21 + or - 9 x one trillion g NH4+-N/yr. Another fraction may be removed by absorption on vegetation and soils.

A comparison of heart rate variability, n-3 PUFA status and lipid mediator profile in age- and BMI-matched middle-aged vegans and omnivores.

Science.gov (United States)

Pinto, Ana M; Sanders, Thomas A B; Kendall, Alexandra C; Nicolaou, Anna; Gray, Robert; Al-Khatib, Haya; Hall, Wendy L

2017-03-01

Low heart rate variability (HRV) predicts sudden cardiac death. Long-chain (LC) n-3 PUFA (C20-C22) status is positively associated with HRV. This cross-sectional study investigated whether vegans aged 40-70 years (n 23), whose diets are naturally free from EPA (20 : 5n-3) and DHA (22 : 6n-3), have lower HRV compared with omnivores (n 24). Proportions of LC n-3 PUFA in erythrocyte membranes, plasma fatty acids and concentrations of plasma LC n-3 PUFA-derived lipid mediators were significantly lower in vegans. Day-time interbeat intervals (IBI), adjusted for physical activity, age, BMI and sex, were significantly shorter in vegans compared with omnivores (mean difference -67 ms; 95 % CI -130, -3·4, P50 % and high-frequency power) were similarly lower in vegans, with no differences during sleep. In conclusion, vegans have higher 24 h SDNN, but lower day-time HRV and shorter day-time IBI relative to comparable omnivores. Vegans may have reduced availability of precursor markers for pro-resolving lipid mediators; it remains to be determined whether there is a direct link with impaired cardiac function in populations with low-n-3 status.

Achieving low effluent NO3-N and TN concentrations in low influent chemical oxygen demand (COD) to total Kjeldahl nitrogen (TKN) ratio without using external carbon source

Science.gov (United States)

Cao, Jiashun; Oleyiblo, Oloche James; Xue, Zhaoxia; Otache, Y. Martins; Feng, Qian

2015-07-01

Two mathematical models were used to optimize the performance of a full-scale biological nutrient removal (BNR) activated treatment plant, a plug-flow bioreactors operated in a 3-stage phoredox process configuration, anaerobic anoxic oxic (A2/O). The ASM2d implemented on the platform of WEST2011 software and the BioWin activated sludge/anaerobic digestion (AS/AD) models were used in this study with the aim of consistently achieving the designed effluent criteria at a low operational cost. Four ASM2d parameters (the reduction factor for denitrification , the maximum growth rate of heterotrophs (µH), the rate constant for stored polyphosphates in PAOs ( q pp), and the hydrolysis rate constant ( k h)) were adjusted. Whereas three BioWin parameters (aerobic decay rate ( b H), heterotrophic dissolved oxygen (DO) half saturation ( K OA), and Y P/acetic) were adjusted. Calibration of the two models was successful; both models have average relative deviations (ARD) less than 10% for all the output variables. Low effluent concentrations of nitrate nitrogen (N-NO3), total nitrogen (TN), and total phosphorus (TP) were achieved in a full-scale BNR treatment plant having low influent chemical oxygen demand (COD) to total Kjeldahl nitrogen (TKN) ratio (COD/TKN). The effluent total nitrogen and nitrate nitrogen concentrations were improved by 50% and energy consumption was reduced by approximately 25%, which was accomplished by converting the two-pass aerobic compartment of the plug-flow bioreactor to anoxic reactors and being operated in an alternating mode. Findings in this work are helpful in improving the operation of wastewater treatment plant while eliminating the cost of external carbon source and reducing energy consumption.

Effects of K3[Fe(CN)6] slurry's pH value and applied potential on tungsten removal rate for chemical-mechanical planarization application

Energy Technology Data Exchange (ETDEWEB)

Akonko, S.B.; Li, D.Y.; Ziomek-Moroz, M.; Hawk, J.A.; Miller, A.; Cadien, K.

2005-07-01

Chemical-mechanical planarization (CMP) is an important process for building multilevel interconnections for electronic devices. Directly planarizing tungsten, which is used as via or contact in microelectronic circuits, by wear is a difficult process because of its high hardness. Therefore, an effective approach has been developed to facilitate planarizing tungsten surface by removing a continuously growing passive film on tungsten when exposed to a low-pH potassium ferricyanide slurry. Since the passive film is softer than tungsten, this chemical mechanical planarization process is effective. In this work, in order to determine effects of corrosion and wear on tungsten removal rate, attempts were made to investigate corrosion, wear, and corrosive wear behavior of tungsten in K3[Fe(CN)6] slurries. Electrochemical and tribological experiments were carried out for different slurry pH values and potentials using a rotating pin-on-disc tribometer. Scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) were employed to characterize surface films formed at the different pH levels and potentials. It was demonstrated that the tungsten removal rate increased with increasing slurry pH and potential. Mechanisms involved are discussed.

Improved solar light stimulated charge separation of g-C3N4 through self-altering acidic treatment

Science.gov (United States)

Leong, Kah Hon; Lim, Ping Feng; Sim, Lan Ching; Punia, Varun; Pichiah, Saravanan

2018-02-01

Herein, we report the use of acid treatment to treat g-C3N4 nanostructured by a direct and facile synthesis route. The adopted treatment enhanced photoactivity of g-C3N4 and reflected in the removal of recalcitrant organic pollutant, Bisphenol A under direct sunlight. A complete removal of Bisphenol A was attained in a short duration (225 min) as compared to pure g-C3N4. The analysis clearly substantiated the robustness of acid exfoliation that promoted a blue shift, extended the conjugated length of its respective conduction and valance band. It also drastically prolonged the recombination rate of charge carriers, by producing excess of unpaired electrons in the conduction band for active radicals' generation. Thus, this new findings could offer a new sight of self-alteration in improving the photoactivity of complex organic pollutants for sustainable environmental remediation.

Impact of hydraulic and carbon loading rates of constructed wetlands on contaminants of emerging concern (CECs) removal

International Nuclear Information System (INIS)

Sharif, Fariya; Westerhoff, Paul; Herckes, Pierre

2014-01-01

Constructed wetlands remove trace organic contaminants via synergistic processes involving plant biomass that include hydrolysis, volatilization, sorption, biodegradation, and photolysis. Wetland design conditions, such as hydraulic loading rates (HLRs) and carbon loading rates (CLRs), influence these processes. Contaminant of emerging concern (CEC) removal by wetland plants was investigated at varying HLRs and CLRs. Rate constants and parameters obtained from batch-scale studies were used in a mechanistic model to evaluate the effect of these two loading rates on CEC removal. CLR significantly influenced CEC removal when wetlands were operated at HLR >5 cm/d. High values of CLR increased removal of estradiol and carbamazepine but lowered that of testosterone and atrazine. Without increasing the cumulative HLR, operating two wetlands in series with varying CLRs could be a way to improve CEC removal. -- Highlights: • A fate-predictive model was developed to evaluate the effect of loading rates on CEC removal in constructed wetlands. • Carbon loading rates (CLRs) can influence CEC removal when wetlands are operated at higher hydraulic loading rates (HLRs). • The effect of CLRs varies among CECs with different physico-chemical properties. • Combination of wetlands with different CLRs can optimize CEC removal without changing the net HLR. -- This article evaluates the effect of design loading rates on contaminant of emerging concern (CEC) removal in constructed wetlands

Low-level NOx removal in ambient air by pulsed corona technology

International Nuclear Information System (INIS)

Beckers, F J C M; Hoeben, W F L M; Pemen, A J M; Van Heesch, E J M

2013-01-01

Although removal of NO x by (pulsed) corona discharges has been thoroughly investigated for high concentrations of NO x in flue gas, removal of low levels in ambient air proves to be a difficult task. (Sub) ppm NO x levels exist in traffic tunnels due to accumulation of exhaust gases. The application of pulsed corona technology for purification of traffic tunnel air is studied during a series of lab and field experiments. An industrial pilot scale wire-cylinder type corona reactor has been utilized. Lab tests have been carried out using a diesel generator as NO x source. NO x conversion levels have been determined by applying two Recordum Airpointers (chemiluminescence-based detection). The detector appeared to be cross-sensitive for HNO 3 and high levels of O 3 . NO x removal rates of 60–80% were obtained for inlet levels of 2–10 ppm. The SIE value of 10 ppm NO x removal is 7 J l −1 . The corona discharges produce ppm level NO x at high energy densities. This intrinsic NO x production limits removal of inlet levels due to equilibrium between production and oxidation. (paper)

High-rate oil removing scouring agent. Koyubun jokyoyo seirenzai ni tsuite

Energy Technology Data Exchange (ETDEWEB)

Ishihara, K.; Sato, Y. (Dai-Ichi Kogyo Seiyaku Co. Ltd., Kyoto (Japan))

1991-11-01

Fiber forming, scutching and knitting processes in recent years are performed three to five times faster than in the conventional processes. Associated therewith, oil solutions are taken importantly for their stability and workability, such as smoothing properties, heat resistance and abrasion resistance. On the other hand, difficulty is increasing in removing the oils after scutching and knitting. This paper explains basic rinsing activities required in oil removal, and describes various test characteristics and compatibility of various high-rate oil removing scouring agents. An oil-in-water rinsing mechanism relies upon comprehensive actions of a surfactant in wetting, permeation, emulsified dispersion and solubilization. The most importantly taken among them is the emulsifying action, which largely depends upon its chemical structure. Therefore, for a high-rate oil removing scouring agent, creation of activators is required that make the above basic characteristics and activities compatible for various applications. For example, the above product covers a great variety of kinds for diverse applications, based on non-ionic and anion-based activators. 6 figs., 20 tabs.

Comparison between coagulation-flocculation and ozone-flotation for Scenedesmus microalgal biomolecule recovery and nutrient removal from wastewater in a high-rate algal pond.

Science.gov (United States)

Oliveira, Gislayne Alves; Carissimi, Elvis; Monje-Ramírez, Ignacio; Velasquez-Orta, Sharon B; Rodrigues, Rafael Teixeira; Ledesma, María Teresa Orta

2018-07-01

The removal of nutrients by Scenedesmus sp. in a high-rate algal pond, and subsequent algal separation by coagulation-flocculation or flotation with ozone to recover biomolecules, were evaluated. Cultivation of Scenedesmus sp. in wastewater resulted in complete NH 3 -H removal, plus 93% total nitrogen and 61% orthophosphate removals. Ozone-flotation obtained better water quality results than coagulation-flocculation for most parameters (NH 3 -N, NTK, nitrate and nitrite) except orthophosphate. Ozone-flotation, also produced the highest recovery of lipids, carbohydrates and proteins which were 0.32 ± 0.03, 0.33 ± 0.025 and 0.58 ± 0.014 mg/mg of biomass, respectively. In contrast, there was a low lipid extraction of 0.21 mg of lipids/mg of biomass and 0.12-0.23 mg of protein/mg of biomass in the coagulation-flocculation process. In terms of biomolecule recovery and water quality, ozone showed better results than coagulation-flocculation. Copyright © 2018 Elsevier Ltd. All rights reserved.

Synthesis of 3H-3-azido-salicyl-N-(n-decyl) amide

International Nuclear Information System (INIS)

Lu Bin; Xu Jianxing; Chen Shizhi

2000-01-01

A novel method for the synthesis of molecular probe of ubiquinone-binding protein is described. With 3-nitrosalicylic acid and decylamine as initial compounds and under the existence of DCC, the 3-nitro-salicyl-N-(n-decyl)amide is synthesized at room temperature. Then, 3-nitro-salicyl-N-(n-decyl)amide is reduced by hydrogen with 5 % Pd/C as catalyst to form 3-amino-salicyl-N-(n-decyl)amide which is exchanged with tritium to be 3 H-3-amino-salicyl-N-(n-decyl)amide. At the temperature below 5 degree C, 3 H-3-amino-salicyl-N-(n-decyl)amide reacts with NaNO 2 and HCl, and the 3-diazo-salicyl-N-(n-decyl)amide is formed in an ice salt bath. As soon as the reaction is completed, NaN 3 is added to the mixture and stirred for 3 h at the temperature between 0 - 5 degree C and in the dark, the molecular probe of studying ubiquinone-binding protein, i. e., 3 H-3-azido-salicyl-N-(n-decyl)amide is produced

Effects of NO3(-) and NH4(+) and urea on each other's uptake and incorporation

Science.gov (United States)

Huffaker, R. C.; Ward, M. R.

1986-01-01

The purpose was to determine the optimal use by wheat plants of the N sources expected from processing biological waste products, NO3(-),NO2(-)NH4(+), and urea. The approach was to determine the uptake and metabolic products of each N source (from single and multiple component solutions), inhibitory effects of each, feedback inhibition, and overall in vivo regulation of the rates of assimilation of each by wheat plants. Previously, researchers determined the interactions of NO3(-),NO2(-),NH4(+) on each other's uptake and incorporation. The assimilation and some of its effects on NO3(-) and NH4(+) assimilation which have been completed to data are discussed.

Ammonia removal in electrochemical oxidation: Mechanism and pseudo-kinetics

International Nuclear Information System (INIS)

Li Liang; Liu Yan

2009-01-01

This paper investigated the mechanism and pseudo-kinetics for removal of ammonia by electrochemical oxidation with RuO 2 /Ti anode using batch tests. The results show that the ammonia oxidation rates resulted from direct oxidation at electrode-liquid interfaces of the anode by stepwise dehydrogenation, and from indirect oxidation by hydroxyl radicals were so slow that their contribution to ammonia removal was negligible under the condition with Cl - . The oxidation rates of ammonia ranged from 1.0 to 12.3 mg N L -1 h -1 and efficiency reached nearly 100%, primarily due to the indirect oxidation of HOCl, and followed pseudo zero-order kinetics in electrochemical oxidation with Cl - . About 88% ammonia was removed from the solution. The removed one was subsequently found in the form of N 2 in the produced gas. The rate at which Cl - lost electrons at the anode was a major factor in the overall ammonia oxidation. Current density and Cl - concentration affected the constant of the pseudo zero-order kinetics, expressed by k = 0.0024[Cl - ] x j. The ammonia was reduced to less than 0.5 mg N L -1 after 2 h of electrochemical oxidation for the effluent from aerobic or anaerobic reactors which treated municipal wastewater. This result was in line with the strict discharge requirements

[Phylogenetic analysis and nitrogen removal characteristics of a heterotrophic nitrifying-aerobic denitrifying bacteria strain from marine environment].

Science.gov (United States)

Sun, Xuemei; Li, Qiufen; Zhang, Yan; Liu, Huaide; Zhao, Jun; Qu, Keming

2012-06-04

We determined the phylogenetic position of a heterotrophic nitrifying-aerobic denitrifying bacterium X3, and detected its nitrogen removal characteristics for providing evidence to explain the principle of heterotrophic nitrification-aerobic denitrification and to improve the process in purification of marine-culture wastewater. The evolutionary position of the strain was determined based on its morphological, physiological, biochemical characteristics and 16SrRNA gene sequence. The nitrification-denitrification ability of this strain was detected by detecting its nitrogen removal efficiency and growth on different inorganic nitrogen source. Strain X3 was identified as Halomonas sp. It grew optimally at salinity 3%, pH 8.5, C:N 10:1 at 28 degrees C, and it could still survive at 15% salinity. The removal of NH4+ -N, NO2(-) -N and NO3(-) -N was 98.29%, 99.07%, 96.48% respectively within 24 h. When three inorganic nitrogen existed simultaneously, it always utilized ammonia firstly, and the total inorganic nitrogen removal was higher than with only one nitrogen, suggesting that strain X3 has the ability of simultaneous nitrification and denitrification and completing the whole nitrogen removing process. Strain X3 belonged to the genus of Halomonas. It had strong simultaneous nitrification and denitrification capability and could live in high-salinity environment.

Nitrogen removal in Northern peatlands treating mine wastewaters

Science.gov (United States)

Palmer, Katharina; Karlsson, Teemu; Turunen, Kaisa; Liisa Räisänen, Marja; Backnäs, Soile

2015-04-01

Natural peatlands can be used as passive purification systems for mine wastewaters. These treatment peatlands are well-suited for passive water treatment as they delay the flow of water, and provide a large filtration network with many adsorptive surfaces on plant roots or soil particles. They have been shown to remove efficiently harmful metals and metalloids from mine waters due to variety of chemical, physical and biological processes such as adsorption, precipitation, sedimentation, oxidation and reduction reactions, as well as plant uptake. Many factors affect the removal efficiency such as inflow water quality, wetland hydrology, system pH, redox potential and temperature, the nature of the predominating purification processes, and the presence of other components such as salts. However, less attention has been paid to nitrogen (N) removal in peatlands. Thus, this study aimed to assess the efficiency of N removal and seasonal variation in the removal rate in two treatment peatlands treating mine dewatering waters and process effluent waters. Water sampling from treatment peatland inflow and outflow waters as well as pore waters in peatland were conducted multiple times during 2012-2014. Water samples were analysed for total N, nitrate-N and ammonium-N. Additionally, an YSI EXO2 device was used for continuous nitrate monitoring of waters discharged from treatment peatlands to the recipient river during summer 2014. The results showed that the oxic conditions in upper peat layer and microbial activity in treatment peatlands allowed the efficient oxidation of ammonium-N to nitrite-N and further to nitrate-N during summer time. However, the slow denitrification rate restricts the N removal as not all of the nitrate produced during nitrification is denitrified. In summer time, the removal rate of total N varied between 30-99 % being highest in late summer. N removal was clearly higher for treatment peatland treating process effluent waters than for peatland

Scaling in Rate-Changeable Birth and Death Processes with Random Removals

International Nuclear Information System (INIS)

Ke Jianhong; Lin Zhenquan; Chen Xiaoshuang

2009-01-01

We propose a monomer birth-death model with random removals, in which an aggregate of size k can produce a new monomer at a time-dependent rate I(t)k or lose one monomer at a rate J(t)k, and with a probability P (t) an aggregate of any size is randomly removed. We then analytically investigate the kinetic evolution of the model by means of the rate equation. The results show that the scaling behavior of the aggregate size distribution is dependent crucially on the net birth rate I(t) - J(t) as well as the birth rate I(t). The aggregate size distribution can approach a standard or modified scaling form in some cases, but it may take a scale-free form in other cases. Moreover, the species can survive finally only if either I(t) - J(t) ≥ P (t) or [J(t) + P (t) - I(t)]t ≅ 0 at t >> 1; otherwise, it will become extinct.

Nitrate movement and removal along a shallow groundwater flow path in a riparian wetland within a sheep-grazed pastoral catchment : result of a tracer study

International Nuclear Information System (INIS)

Burns, D.A.; Nguyen, L.

2002-01-01

The movement and removal of nitrate (NO 3 ) along a groundwater flow path within a riparian wetland was investigated during a 24-day period in late autumn-early winter, using a lithium bromide (LiBr)-potassium nitrate (KNO 3 ) tracer solution containing 19 200 mg/litre as Br - and 193.8 mg/litre as NO 3 -N. The tracer solution was added as an instantaneous dose of tracer solution at a depth of 10-20 cm to four injection wells in two 1 m 2 plots within a sheep-grazed pastoral catchment at the Whatawhata Agricultural Research Centre near Hamilton, New Zealand. Bromide and NO 3- N concentrations were measured periodically in: (1) wetland groundwater samples from piezometers installed at 15 and 30 cm depths and located at 30, 60, and 100 cm down gradient from the injection wells; and (2) surface flow samples. Peak concentrations of 50-250 mg/litre of Br - and 0.2-1.1 mg/litre of NO 3 -N were reached within 1-2 days after application at most piezometers. Nitrate concentrations decreased thereafter more sharply than did those of Br - , resulting in decreased NO 3 -N/Br - ratios from Days 2 through 7. More than 99% of groundwater samples collected after the tracer application had NO 3 -N/Br - less than the value in the tracer solution indicating removal of NO 3 -N during transport. Mass flux estimates indicated removal of >90% of added NO 3 -N along the 100 cm flow path from the injection, with essentially all of the NO 3 - removed within the first 30 cm of transport. On Days 10 and 24, just after rain events, surface flow from the experimental plots had greatly elevated NO 3 -N concentrations that were not accompanied by correspondingly elevated Br - concentrations, indicating that NO 3 -N originating from the surrounding catchment was transported over the wetland surface with little penetration or mixing with wetland groundwater. Despite a significant capacity for NO 3 -N removal from shallow groundwater equivalent to an annualised value of 50 kg/ha in these wetland

Thermophilic co-digestion feasibility of distillers grains and swine manure: effect of C/N ratio and organic loading rate during high solid anaerobic digestion (HSAD).

Science.gov (United States)

Sensai, P; Thangamani, A; Visvanathan, C

2014-01-01

Anaerobic co-digestion of high solids containing distillers grains and swine manure (total solids, 27 +/- 2% and 18 +/- 2%, respectively) was evaluated in this study to assess the effect of C/N ratio and organic loading rate (OLR). Feed mixture was balanced to achieve a C/N ratio of 30/1 by mixing distillers grains and swine manure. Pilot-scale co-digestion of distillers grains and swine manure was carried out under thermophilic conditions in the continuous mode for seven different OLRs from R1 to R7 (3.5, 5, 6, 8, 10, 12 and 14 kg VS/m3 day) under high solid anaerobic digestion. The methane yield and volatile solid (VS) removal were consistent; ranging from 0.33 to 0.34 m3CH4/kg VS day and 50-53%, respectively, until OLR 8 kg VS/m3 day. After which methane yield and VS removal significantly decreased to 0.26 m3 CH4/kg VS day and 42%, respectively, when OLR was increased to 14 kg VS/m3 day. However, during operation, at OLR of 10 kg VS/m3 day, the methane yield and VS removal increased after the 19th day to 0.33 m3 CH4/kg VS day and 46%, respectively, indicating that a longer acclimatization period is required by methanogens at a higher loading rate.

Laser-induced removal of a dye C.I. Acid Red 87 using n-type WO{sub 3} semiconductor catalyst

Energy Technology Data Exchange (ETDEWEB)

Qamar, M. [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Gondal, M.A., E-mail: magondal@kfupm.edu.sa [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Laser Research Laboratory, Physics Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Hayat, K. [Chemistry Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Yamani, Z.H. [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Laser Research Laboratory, Physics Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Al-Hooshani, K. [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Chemistry Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia)

2009-10-30

Water contamination by organic substances such as dyes is of great concern worldwide due to their utilization in many industrial processes and environmental concerns. To cater the needs for waste water treatment polluted with organic dyes, laser-induced photocatalytic process was investigated for removal of a dye derivative namely Acid Red 87 using n-type WO{sub 3} semiconductor catalyst. The degradation was investigated in aqueous suspensions of tungsten oxide under different experimental conditions using laser instead of conventional UV lamp as an irradiation source. The degradation process was monitored by measuring the change in dye concentration as a function of laser irradiation time by employing UV spectroscopic analysis. The degradation of dye was studied by varying different parameters such as laser energy, reaction pH, substrate concentration, catalyst concentration, and in the presence of electron acceptors such as hydrogen peroxide (H{sub 2}O{sub 2}), and potassium bromate (KBrO{sub 3}). The degradation rates were found to be strongly dependent on all the above-mentioned parameters. Our experimental results revealed that the dye degradation process was very fast (within few minutes) under laser irradiation as compared to conventional setups using broad spectral lamps (hours or days) and this laser-induced photocatalytic degradation method could be an effective means to eliminate the pollutants present in liquid phase. The experience gained through this study could be beneficial for treatment of waste water contaminated with organic dyes and other organic pollutants.

Cyclic Nanostructures of Tungsten Oxide (WO3) n   (n = 2-6) as NO x Gas Sensor: A Theoretical Study.

Science.gov (United States)

Izadyar, Mohammad; Jamsaz, Azam

2014-01-01

Today's WO3-based gas sensors have received a lot of attention, because of important role as a sensitive layer for detection of the small quantities of  NO x . In this research, a theoretical study has been done on the sensing properties of different cyclic nanoclusters of (WO3) n   (n = 2-6) for NO x   (x = 1,2) gases. Based on the calculated adsorption energies by B3LYP and X3LYP functionals, from the different orientations of  NO x molecule on the tungsten oxide clusters, O-N⋯W was preferred. Different sizes of the mentioned clusters have been analyzed and W2O6 cluster was chosen as the best candidate for NO x detection from the energy viewpoint. Using the concepts of the chemical hardness and electronic charge transfer, some correlations between the energy of adsorption and interaction energy have been established. These analyses confirmed that the adsorption energy will be boosted with charge transfer enhancement. However, the chemical hardness relationship is reversed. Finally, obtained results from the natural bond orbital and electronic density of states analysis confirmed the electronic charge transfer from the adsorbates to WO3 clusters and Fermi level shifting after adsorption, respectively. The last parameter confirms that the cyclic clusters of tungsten oxide can be used as NO x gas sensors.

Simultaneous removal of ammonia and N-nitrosamine precursors from high ammonia water by zeolite and powdered activated carbon.

Science.gov (United States)

Xue, Runmiao; Donovan, Ariel; Zhang, Haiting; Ma, Yinfa; Adams, Craig; Yang, John; Hua, Bin; Inniss, Enos; Eichholz, Todd; Shi, Honglan

2018-02-01

When adding sufficient chlorine to achieve breakpoint chlorination to source water containing high concentration of ammonia during drinking water treatment, high concentrations of disinfection by-products (DBPs) may form. If N-nitrosamine precursors are present, highly toxic N-nitrosamines, primarily N-nitrosodimethylamine (NDMA), may also form. Removing their precursors before disinfection should be a more effective way to minimize these DBPs formation. In this study, zeolites and activated carbon were examined for ammonia and N-nitrosamine precursor removal when incorporated into drinking water treatment processes. The test results indicate that Mordenite zeolite can remove ammonia and five of seven N-nitrosamine precursors efficiently by single step adsorption test. The practical applicability was evaluated by simulation of typical drinking water treatment processes using six-gang stirring system. The Mordenite zeolite was applied at the steps of lime softening, alum coagulation, and alum coagulation with powdered activated carbon (PAC) sorption. While the lime softening process resulted in poor zeolite performance, alum coagulation did not impact ammonia and N-nitrosamine precursor removal. During alum coagulation, more than 67% ammonia and 70%-100% N-nitrosamine precursors were removed by Mordenite zeolite (except 3-(dimethylaminomethyl)indole (DMAI) and 4-dimethylaminoantipyrine (DMAP)). PAC effectively removed DMAI and DMAP when added during alum coagulation. A combination of the zeolite and PAC selected efficiently removed ammonia and all tested seven N-nitrosamine precursors (dimethylamine (DMA), ethylmethylamine (EMA), diethylamine (DEA), dipropylamine (DPA), trimethylamine (TMA), DMAP, and DMAI) during the alum coagulation process. Copyright © 2017. Published by Elsevier B.V.

Removal of micropollutants during tertiary wastewater treatment by biofiltration: Role of nitrifiers and removal mechanisms.

Science.gov (United States)

Rattier, M; Reungoat, J; Keller, J; Gernjak, W

2014-05-01

The objective of this study was to determine the extent to which a suite of organic micropollutants (MPs) can be removed by biological filtration and the role of bioavailability and ammonia oxidizing microorganisms (AOMs) in the biodegradation process. During approximately one year, laboratory-scale columns with 8 min empty bed contact time (EBCT) and packed with anthracite as filter media were used for treating a tertiary effluent spiked with a broad range of MPs at a target concentration of 2 μg L(-1). In parallel columns, aerobic biomass growth was inhibited by using either the biocide sodium azide (500 mg L(-1) NaN3) or allylthiourea (5 mg L(-1) ATU), specifically inhibiting nitrifying bacteria. Once the biomass had colonized the media, around 15% of the dissolved organic carbon (DOC) contained in the untreated tertiary effluent was removed by non-inhibited columns. The removal of several MPs increased over time indicating the relevance of biological activity for the removal of MPs, while the negative control, the NaN3 inhibited column, showed no significant removal. Out of 33 MPs, 19 were recalcitrant (granular activated carbon (GAC) and their removal efficiency by biodegradation on anthracite was observed. This result suggested that the affinity of the MPs for GAC media could be a useful indicator of the bioavailability of compounds during biofiltration on anthracite. Copyright © 2014 Elsevier Ltd. All rights reserved.

Nitrogen removal in a SBR operated with and without pre-denitrification: effect of the carbon:nitrogen ratio and the cycle time.

Science.gov (United States)

Mees, Juliana Bortoli Rodrigues; Gomes, Simone Damasceno; Hasan, Salah Din Mahmud; Gomes, Benedito Martins; Boas, Márcio Antonio Vilas

2014-01-01

The effects of cycle time (CT) (8, 12 and 16h) and C/N ratio (3, 6 and 9) on nitrogen removal efficiencies in a bench top sequencing batch reactor treating slaughterhouse wastewater were investigated under different operating conditions: in condition 1, the reaction comprises an aerobic/anoxic phase and in condition II, the reaction comprises anoxic I/aerobic/anoxic II phases (with pre-denitrification). The greatest percentages of nitrogen removal were obtained in the CT range from 12 to 16 h and C/N ratios from 3 to 6, with mean efficiency values of 80.76% and 85.57% in condition I and 90.99% and 91.09% in condition II. Although condition II gave a higher removal of total inorganic nitrogen (NH4+ - N + NO2- - N + NO3- - N) than condition I, only condition I showed statistically significant and predictive regression for all the steps of nitrogen removal.

Heavy metal removal using nanoscale zero-valent iron (nZVI): Theory and application

Energy Technology Data Exchange (ETDEWEB)

Li, Shaolin, E-mail: lishaolin@tongji.edu.cn; Wang, Wei; Liang, Feipeng; Zhang, Wei-xian, E-mail: zhangwx@tongji.edu.cn

2017-01-15

Highlights: • nZVI is able to perform fast and simultaneous removal of different heavy metal ions. • Fast separation and seeding effect of nZVI facilities its application in wastewater. • A novel process of E{sub h}-controlled reactor, nZVI separator and reuse is proposed. • E{sub h}-controlled system and nZVI recirculation increase material efficiency of nZVI. • The process produces stable effluent and is effective in wastewater treatment. - Abstract: Treatment of wastewater containing heavy metals requires considerations on simultaneous removal of different ions, system reliability and quick separation of reaction products. In this work, we demonstrate that nanoscale zero-valent iron (nZVI) is an ideal reagent for removing heavy metals from wastewater. Batch experiments show that nZVI is able to perform simultaneous removal of different heavy metals and arsenic; reactive nZVI in uniform dispersion brings rapid changes in solution E{sub h}, enabling a facile way for reaction regulation. Microscope characterizations and settling experiments suggest that nZVI serves as solid seeds that facilitate products separation. A treatment process consisting of E{sub h}-controlled nZVI reaction, gravitational separation and nZVI recirculation is then demonstrated. Long-term (>12 months) operation shows that the process achieves >99.5% removal of As, Cu and a number of other toxic elements. The E{sub h}-controlled reaction system sustains a highly-reducing condition in reactor and reduces nZVI dosage. The process produces effluent of stable quality that meets local discharge guidelines. The gravitational separator shows high efficacy of nZVI recovery and the recirculation improves nZVI material efficiency, resulting in extraordinarily high removal capacities ((245 mg As + 226 mg-Cu)/g-nZVI). The work provides proof that nanomaterials can offer truly green and cost-effective solutions for wastewater treatment.

NO3-/NH4+ ratios affect nutritional homeostasis and production of Tanzania guinea grass under Cu toxicity.

Science.gov (United States)

de Souza Junior, João Cardoso; Nogueirol, Roberta Corrêa; Monteiro, Francisco Antonio

2018-05-01

Nitrogen (N) can alleviate metal toxicity. However, as of yet, there have been no studies showing the efficacy of NO 3 - /NH 4 + in mitigating Cu toxicity. The objective of this study was to evaluate the Cu toxicity on the nutritional and productive attributes of Panicum maximum cv. Tanzania as well as the role of NO 3 - and NH 4 + ratios in nutritional homeostasis. The experiment was conducted using 3 × 4 factorial treatments arranged in a randomized complete block design with three replicates. The treatments were three NO 3 - /NH 4 + ratios (100/0, 70/30, and 50/50) and four Cu rates (0.3, 250, 500, and 1000 μmol L -1 ) in nutrient solution. Copper concentrations in the diagnostic leaves (DL) were highest in plants grown under 70/30 NO 3 - /NH 4 + ratios and a Cu rate of 1000 μmol L -1 . In this combination, it was observed that DL had higher concentrations of NH 4 + , greater glutamine synthetase activity, lower chlorophyll concentration (SPAD value), and lower shoot dry mass, suggesting high disorders of nutritional homeostasis. Plants receiving N in the form of NO 3 - and 1000 Cu μmol L -1 showed that DL had lower concentrations of Cu, higher concentration of chlorophyll, higher NO 3 - concentration, higher nitrate reductase activity, and higher NO 3 - accumulation in the roots, suggesting a reduction in disorders of nutritional homeostasis. The disorders on mineral uptake, N assimilation, and biomass production caused by Cu toxicity are shown to be affected by NO 3 - /NH 4 + ratios, and N supply via NO 3 - allowed for better homeostasis of the forage grass.

Addition compounds between lanthanide (III) and yttrium (III) and methanesulfonates (MS) and 3-picoline-N-oxide (3-pic NO)

International Nuclear Information System (INIS)

Zinner, L.B.

1984-01-01

The preparation and characterization of addition compounds between lanthanide methanesulfonates and 3-picoline-N-oxide of general formula Ln (MS) 3 .2(3-pic No), Ln being La, Yb and Y, were carried out. The techniques employed for characterization were: elemental analysis, X-ray diffraction, infrared absorption spectroscopy, electrolytic conductance in methanol, melting ranges and emission spectrum of the Eu (III) compound. (Author) [pt

Virus removal during groundwater recharge: effects of infiltration rate on adsorption of poliovirus to soil.

OpenAIRE

Vaughn, J M; Landry, E F; Beckwith, C A; Thomas, M Z

1981-01-01

Studies were conducted to determine the influence of infiltration rate on poliovirus removal during groundwater recharge with tertiary-treated wastewater effluents. Experiments were conducted at a uniquely designed, field-situated test recharge basin facility through which some 62,000 m3 of sewage had been previously applied. Recharge at high infiltration rates (75 to 100 cm/h) resulted in the movement of considerable numbers of seeded poliovirus to the groundwater. Moderately reduced infiltr...

Physiological Responses to N-NO3 and N-NH4 of Triazine Resistant and Susceptible Plants of Horseweed (Erigeron canadensis L.

Directory of Open Access Journals (Sweden)

Ryszard Stanek

2013-12-01

Full Text Available Triazine resistant and susceptible biotypes of horseweed (Erigeron canadensis L. were grown under controlled conditions in nutrient solution with NH4 or NO3 ions as nitrogen source. Indicators such as: dry matter, CO2 assimilation, chloroplasts activity, dark respiration and the content of K, Ca, Mg in the above ground parts displayed lower levels when plants were fed with NH4 than with NO ions. Reduction of these indicators was stronger for the triazine susceptible plants which grew better than their resistant counterparts when fed with N-NO3. The triazine resistant plants grown with N-NH4 contained more protein-N and K than the susceptible ones. Chloroplasts of the resistant plants were also less sensitive to NH4CL treatment. It is concluded that the resistant plants appear to be more tolerant to NH4 ions as compared with their susceptible counterparts. For this reason application of ammonium forms of nitrogen fertilization in horticultural practice could favour spreading of triazine resistant horseweed.

Selecting appropriate forms of nitrogen fertilizer to enhance soil arsenic removal by Pteris vittata: a new approach in phytoremediation.

Science.gov (United States)

Liao, Xiao-Yong; Chen, Tong-Bin; Xiao, Xi-Yuan; Xie, Hua; Yan, Xiu-Lan; Zhai, Li-Mei; Wu, Bin

2007-01-01

Certain plant species have been shown to vigorously accumulate some metals from soil, and thus represent promising and effective remediation alternatives. In order to select the optimum forms of nitrogen (N) fertilizers for the arsenic (As) hyperaccumulator, Pteris vittata L., to maximize As extraction, five forms of N were added individually to different treatments to study the effect of N forms on As uptake of the plants under soil culture in a greenhouse. Although shoot As concentration tended to decrease and As translocation from root to shoot was inhibited, overall As accumulation was greater due to higher biomass when N fertilizer was added. Arsenic accumulation in plants with N fertilization was 100-300% more than in the plants without N fertilization. There were obvious differences in plant biomass and As accumulation among the N forms, i.e., NH4HCO3, (NH4)2S04, Ca(NO3)2, KNO3, urea. The total As accumulation in the plants grown in As-supplied soil, under different forms of N fertilizer, decreased as NH4HCO3>(NH4)2S04 > urea > Ca(NO3)2 >KNO3>CK. The plants treated with N and As accumulated up to 5.3-7.97 mg As/pot and removed 3.7-5.5% As from the soils, compared to approximately 2.3% of As removal in the control. NH4+ -N was apparently more effective than other N fertilizers in stimulating As removal when soil was supplied with As at initiation. No significant differences in available As were found among different forms of N fertilizer after phytoremediation. It is concluded that NH4+ -N was the preferable fertilizer for P. vittata to maximize As removal.

Magnetic bionanoparticles of Penicillium sp. yz11-22N2 doped with Fe3O4 and encapsulated within PVA-SA gel beads for atrazine removal.

Science.gov (United States)

Yu, Jiaping; He, Huijun; Yang, William L; Yang, Chunping; Zeng, Guangming; Wu, Xin

2018-07-01

A novel magnetic bionanomaterial, Penicillium sp. yz11-22N2 doped with nano Fe 3 O 4 entrapped in polyvinyl alcohol-sodium alginate gel beads (PFEPS), was successfully synthesized. The factors including nutrient substance, temperature, pH, initial concentrations of atrazine and rotational speeds were presented and discussed in detail. Results showed that the highest removal efficiency of atrazine by PFEPS was 91.2% at 8.00 mg/L atrazine. The maximum removal capacity for atrazine was 7.94 mg/g. Meanwhile, it has been found that most of atrazine were removed by metabolism and degradation of Penicillium sp. yz11-22N2, which could use atrazine as the sole source of either carbon or nitrogen. Degradation kinetics of atrazine conformed to first-order kinetics model. The intermediates indicated that the possible pathway for atrazine degradation by PFEPS mainly included hydrolysis dechlorination, dealkylation, side-chain oxidation and ring-opening. Copyright © 2018 Elsevier Ltd. All rights reserved.

Advanced treatment technique for swine wastewater using two agents: Thermally polymerized amorphous silica and hydrated lime for color and phosphorus removal and sulfur for nitrogen removal.

Science.gov (United States)

Hasegawa, Teruaki; Kurose, Yohei; Tanaka, Yasuo

2017-10-01

The efficacy of advanced treatment of swine wastewater using thermally polymerized, modified amorphous silica and hydrated lime (M-CSH-lime) for color and phosphorus removal and sulfur for nitrogen removal was examined with a demonstration-scale treatment plant. The color removal rate was approximately 78% at M-CSH-lime addition rates of > 0.055 wt/v%. The PO43--P removal rate exceeded 99.9% with > 0.023 wt/v%. pH of the effluent from the M-CSH-lime reactor increased with the addition rate till a maximum value of 12.7, which was effective in disinfection. The recovered M-CSH-lime would be suitable as a phosphorus fertilizer because the total P 2 O 5 content was approximately 10%. The nitrogen oxide (NOx-N) removal rate by sulfur denitrification increased to approximately 80% when the NOx-N loading rate was around 0.1 kg-N/ton-S/day. It was suggested that the combination of the two processes would be effective in the advanced treatment of swine wastewater. © 2017 Japanese Society of Animal Science.