Dynamics of water soluble phosphorus from surface applied broiler litter

Deionized water is routinely used as an extractant to determine soluble phosphorus (P) in broiler litter, but under N.E. Georgia conditions this technique may underestimate the hazard of P loss in runoff because the alkalinity of the broiler litter-water suspension limits the solubility of P compounds that may be solubilized after being spread on acidic field conditions. In this study under controlled conditions we measured soluble P in thatch and top soil after applying untreated broiler litter, residue of broiler litter after water extraction (WER), or residue of broiler litter after extraction with a 2-(N-morpholino) ethanesulfonic acid (MES) buffer at pH 6 (BER). During the 60 d incubation, the WER released 18 % more Total Dissolved P (TDP) than was determined through a conventional water extraction procedure, whereas the BER released 28 % less TDP than the WER, which reflects the greater amount of TDP removed from the broiler litter by the buffer at pH 6.0. However, the total amount of TDP extracted by the MES buffer, which includes that removed at the initial extraction plus that released during the incubation, was 30 % greater than the total amount of TDP extracted with water from the untreated litter plus the TDP extracted with water from the WER during the incubation. This result suggests the need to fine-tune the solid: liquid ratio and shaking time when the MES buffer is used.     

Enhancing soluble phosphorus removal within buffer strips using industrial by-products

Using industrial by-products (IBPs) in conjunction with buffer strips provides a potentially new strategy for enhancing soluble phosphorus (P) removal from agricultural runoff. Here, we investigate the feasibility of this approach by assessing the P sorption properties of IBPs at different solution-IBPs contact time (1–120 min) and solution pH (3, 5.5, 7.5), as well as possible adverse environmental effects including P desorption or heavy metal mobilisation from IBPs. Batch experiments were carried out on two widely available IBPs in the UK that demonstrated high P sorption capacity but different physicochemical characteristics, specifically ochre and Aluminium (Al) based water treatment residuals (Al-WTR). A series of kinetic sorption–desorption experiments alongside kinetic modelling were used to understand the rate and the mechanisms of P removal across a range of reaction times. The results of the kinetic experiments indicated that P was initially sorbed rapidly to both ochre and Al-WTR, followed by a second phase characterised by a slower sorption rate. The excellent fits of kinetic sorption data to a pseudo-second order model for both materials suggested surface chemisorption as the rate-controlling mechanism. Neither ochre nor Al-WTR released substantial quantities of either P or heavy metals into solution, suggesting that they could be applied to buffer strip soils at recommended rates (≤30 g kg^?1 soil) without adverse environmental impact. Although the rate of P sorption by freshly-generated Al-WTR applied to buffer strips reduced following air-drying, this would not limit its practical application to buffer strips in the field if adequate contact time with runoff was provided.     

Dephosphorylation and quantification of organic phosphorus in poultry litter by purified phytic-acid high affinity Aspergillus phosphohydrolases

Extracellular phosphohydrolases mediate the dephosphorylation of phosphoesters and influence bioavailability and loss of agricultural P to the environment to pose risks of impairment of sensitive aquatic ecosystems. Induction and culture of five strains of Aspergillus were conducted to develop a source of high-affinity and robust phosphohydrolases for detecting environmental P and quantifying bioactive P pools in heterogeneous environmental specimens. Enzyme stability and activity against organic P in poultry litter were evaluated in 71 samples collected across poultry producing regions of Arkansas, Maryland, and Oklahoma of the US Differences existed in strains' adaptability to fermentation medium as they showed a wide range of phytate-degrading activity. Phosphohydrolases from Aspergillus ficuum had highest activity when the strain was cultured on a primarily chemical medium, compared to Aspergillus oryzae which preferred a wheat bran-based organic medium. Kinetics parameters of A. ficuum enzymes (K(m)=210 microM; V(max) of 407 nmol s(-1)) indicated phytic acid-degrading potential equivalent to that of commercial preparations. Purified A. ficuum phosphohydrolases effectively quantified litter bioactive P pools, showing that organic P occurred at an average of 54 (+/-14)% of total P, compared to inorganic phosphates, which averaged 41 (+/-12)%. Litter management and land application options must consider the high water-extractable and organic P concentrations and the biological availability of the organic enzyme-labile P pool. Robustness of A. ficuum enzymes and simplicity of the in situ ligand-based enzyme assay may thus increase routine assessment of litter bioactive P composition to sense for on-farm accumulation of such environmentally-sensitive P forms.     

Combination of biochar amendment and phytoremediation for hydrocarbon removal in petroleum-contaminated soil

Remediation of soils contaminated with petroleum is a challenging task. Four different bioremediation strategies, including natural attenuation, biochar amendment, phytoremediation with ryegrass, and a combination of biochar and ryegrass, were investigated with greenhouse pot experiments over a 90-day period. The results showed that planting ryegrass in soil can significantly improve the removal rate of total petroleum hydrocarbons (TPHs) and the number of microorganisms. Within TPHs, the removal rate of total n-alkanes (45.83 %) was higher than that of polycyclic aromatic hydrocarbons (30.34 %). The amendment of biochar did not result in significant improvement of TPH removal. In contrast, it showed a clear negative impact on the growth of ryegrass and the removal of TPHs by ryegrass. The removal rate of TPHs was significantly lower after the amendment of biochar. The results indicated that planting ryegrass is an effective remediation strategy, while the amendment of biochar may not be suitable for the phytoremediation of soil contaminated with petroleum hydrocarbons.     

Fate of arsenic compounds in poultry litter upon land application

The use of the organic As compound, roxarsone, as an antibiotic additive to poultry feed continues to raise concern over potential negative environmental impacts. Total As concentration in poultry litter can reach >40 mg kg⁻¹ and both roxarsone and its mineralization product As(V) have been identified in poultry litters (PL). To investigate the fate of these As species upon land application of PL we conducted two studies. In the first, an Orangeburg soil (Ultisol from the Atlantic Coastal Plain) was spiked with either 20 mg kg⁻¹ As(V) or roxarsone and incubated at 10% moisture content for 4 months. Exchangeable As was determined periodically by extraction with 0.1 M PO₄. Both As(V) and roxarsone displayed similar desorption; initially, approximately 70% of added As was ligand exchangeable and this decreased to 35% after 4 months incubation, presumably due to either slow sorption reactions or a change in solid phase speciation of As to less exchangeable forms. In the second study, various manipulations of two PL samples were applied to the Orangeburg soil at realistic field application rates. The treatments were wet to 10% moisture content and water soluble As, Cu and organic carbon (DOC) was measured over 30 days. Arsenic and Cu solubility were highest from the dried litter samples. Ashing of the PLs decreased soluble As and Cu, presumably because of the loss of organic matter from the ashed litter and subsequent decrease in DOC. Application of leachates from either PL resulted in higher concentrations of soluble As and Cu than when the soil was amended with equivalent concentrations of soluble As and Cu dissolved in DI H₂O. We hypothesize that the increased levels of DOC from the PL treatments enhance As and Cu solubility through competitive sorption and complexation, respectively. In fact, As and Cu solubility was correlated to DOC levels in the amended soil extracts. Even though land application of PL introduced relatively low concentrations of As and Cu to soil it appeared that other soluble constituents of PL significantly enhanced As and Cu solubility.     

生活污水二级生物处理后的铁盐混凝除磷试验研究

以生活污水二级生物处理后的出水为研究对象,考察了铁盐对浓度在2－4mg/L范围内的总磷的混凝去除效果及影响因素。结果表明,铁盐除磷的最佳pH为7.5-8;铁盐投加量较低时,适当提高GT值可使总磷去除率增加15％－20％;在适当的混凝搅拌条件下,三阶铁盐和聚合硫酸铁对总磷的去除率均在70％以上,混凝后过滤可使出水中总磷降至0.5mg/L以下。     

Enhanced coagulation of ferric chloride aided by tannic acid for phosphorus removal from wastewater

Phosphorus removal from wastewater is of great importance. In the present study, ferric chloride was selected as the coagulant, and tannic acid (TA), a natural polymer, as the coagulant aid to develop an effective coagulation process with the emphasis of phosphorus recovery from different types of wastewater. The results showed that TA can accelerate the settling speed by forming flocs with large size, reduce the residual Fe(III) to eliminate the yellow color caused by Fe(III), and slightly increase the phosphorus removal efficiency. The precipitate formed by TA-aided coagulation showed the advantage of releasing phosphorus faster than ferric phosphate, indicating the possibility of phosphorus recovery from wastewater as slow release fertilizer. To further understand the structural characteristics of the precipitate, analytical techniques such as Raman spectroscopy, X-ray photoelectron spectroscopy and matrix-assisted laser desorption ionization-time of flight mass spectrometry were employed. The analytical results indicated that TA–Fe–P complex was formed during the coagulation/flocculation processes. Solid phase in the precipitate consisted of TA–Fe–P complex, Fe–TA complex and/or ferric hydroxyphosphate.     

Investigation of nitrogen-bearing species in catalytic steam gasification of poultry litter

The production of broiler chickens has become one of the largest sectors in U.S. agriculture, and the growing demand for poultry has led to an annual production growth rate of 5%. With increased demand for poultry, litter management has become a major challenge in the agriculture industry. Although the catalytic steam gasification has been accepted as a possible and feasible method for litter management, concern has been expressed about the presence of nitrogen and phosphorus containing species in the fuel gas and/or in the final solid residue. The possible release of phosphorus as phosphine gas in the fuel gas can have an adverse impact on the environment. Similarly, possible release of ammonia from the nitrogen containing species is also not acceptable. Hence, under partial U.S. Department of Agriculture support, a study was conducted to examine the fate and the environmental impact of the nitrogen- and phosphorus-containing species released during catalytic steam gasification of poultry litter. From various preliminary tests, it was concluded that most (approximately 100%) of the phosphorus would remain in the residue, and some (20-70%) of the nitrogen would end up as ammonia in the fuel gas. The effects of temperature, catalyst loading, and type of catalyst on ammonia liberation were studied in a muffled furnace setup at atmospheric pressure. The fraction of nitrogen released as ammonia was found to decrease with an increase in temperature during pyrolysis and steam gasification. It also decreased with an increase in catalyst loading.     

硫酸铝渣去除水中磷研究

分别以蒸馏水和太湖水为例,研究了硫酸铝渣去除水中磷的能力,并分析了其对水体Al3+、SO24-以及pH的影响.结果表明:(1)除太湖水pH为9.0、10.0两种条件外,随着磷平衡浓度的增加,硫酸铝渣除磷量趋于某一定值,其规律符合Langmuir吸附等温式;太湖水pH为9.0、10.0两种条件下,硫酸铝渣除磷量符合Fre...     

Bioretention column studies of phosphorus removal from urban stormwater runoff.

This study investigated the effectiveness of bioretention as a stormwater management practice using repetitive bioretention columns for phosphorus removal. Bioretention media, with a higher short-term phosphorus sorption capacity, retained more phosphorus from infiltrating runoff after 3 mg/L phosphorus loading. A surface mulch layer prevented clogging after repetitive total suspended solids input. Evidence suggests that long-term phosphorus reactions will regenerate active short-term phosphorus adsorption sites. A high hydraulic conductivity media overlaying one with low hydraulic conductivity resulted in a higher runoff infiltration rate, from 0.51 to 0.16 cm/min at a fixed 15-cm head, and was more efficient in phosphorus removal (85% mass removal) than a profile with low conductivity media over high (63% mass removal). Media extractions suggest that most of the retained phosphorus in the media layers is available for vegetative uptake and that environmental risk thresholds were not exceeded.     

Enhanced biological phosphorus removal and recovery

Activated sludge systems designed for enhanced nutrient removal are based on the principle of altering anaerobic and aerobic conditions for growth of microorganisms with a high capacity of phosphorus accumulation. Most often, filamentous bacteria constitute a component of the activated sludge microflora. The filamentous microorganisms are responsible for foam formation and activated sludge bulking. The results obtained confirm unanimously that the filamentous bacteria have the ability of phosphorus uptake and accumulation as polyphosphates. Hydrodynamic disintegration of the foam microorganisms results in the transfer of phosphorus and metal cations and ammonium-nitrogen into the liquid phase. It was demonstrated that the disintegration of foam permits the removal of a portion of the nutrients in the form of struvite.     

Integrated physicochemical and biological treatment process for fluoride and phosphorus removal from fertilizer plant wastewater

The phosphate fertilizer industry produces highly hazardous and acidic wastewaters. This study was undertaken to develop an integrated approach for the treatment of wastewaters from the phosphate industry. Effluent samples were collected from a local phosphate fertilizer producer and were characterized by their high fluoride and phosphate content. First, the samples were pretreated by precipitation of phosphate and fluoride ions using hydrated lime. The resulting low- fluoride and phosphorus effluent was then treated with the enhanced biological phosphorus removal (EBPR) process to monitor the simultaneous removal of carbon, nitrogen, and phosphorus. Phosphorus removal included a two-stage anaerobic/aerobic system operating under continuous flow. Pretreated wastewater was added to the activated sludge and operated for 160 days in the reactor. The operating strategy included increasing the organic loading rate (OLR) from 0.3 to 1.2 g chemical oxygen demand (COD)/L.d. The stable and high removal rates of COD, NH4(+)-N, and PO4(3-)-P were then recorded. The mean concentrations of the influent were approximately 3600 mg COD/L, 60 mg N/L, and 14 mg P/L, which corresponded to removal efficiencies of approximately 98%, 86%, and 92%, respectively.     

Phosphate complexation model and its implications for chemical phosphorus removal

A phosphate complexation model is developed, in an attempt to understand the mechanistic basis of chemically mediated phosphate removal. The model presented here is based on geochemical reaction modeling techniques and uses known surface reactions possible on hydrous ferric oxide (HFO). The types of surface reactions and their reaction stoichiometry and binding energies (logK values) are taken from literature models of phosphate interactions with iron oxides. The most important modeling parameter is the proportionality of converting moles of precipitated HFO to reactive site density. For well-mixed systems and phosphate exposed to ferric chloride during HFO precipitation, there is a phosphate capacity of 1.18 phosphate ions per iron atom. In poorly mixed systems with phosphate exposed to iron after HFO formation, the capacity decreased to 25% of the well-mixed value. The same surface complexation model can describe multiple data sets, by varying only a single parameter proportional to the availability of reactive oxygen functional groups. This reflects the unavailability of reactive oxygen groups to bind phosphate. Electron microscope images and dye adsorption experiments demonstrate changes in reactive surface area with aging of HFO particles. Engineering implications of the model/mechanism are highlighted.     

Modelling of phosphorus removal from aqueous and wastewater samples using ferric iron

Batch laboratory scale experiments were conducted to investigate the removal of phosphate from aqueous and municipal wastewater samples by addition of FeCl(3).6H(2)O. The effect of pH, Fe-dose and initial phosphate concentration were assessed. Optimum phosphate removal, 63% for 1:1 molar addition of Fe(III) was observed at pH 4.5. However, a 155% excess of Fe-dose was necessary for complete phosphorus removal. Phosphorus removal from municipal wastewater was slightly higher than that observed for the aqueous solutions. A chemical precipitation mathematical model was developed and tested with the available experimental data. The model included a total of 15 chemical reactions and 4 solid phases with the option of single-phase precipitation or two-phase co-precipitation. The resulting system of non-linear algebraic equations was solved numerically, using the Wijngaarden-Dekker-Brent method.     

Particle size distribution predicts particulate phosphorus removal

Particulate phosphorus (PP) is often the largest component of the total phosphorus (P) load in stormwater. Fine-resolution measurement of particle sizes allows us to investigate the mechanisms behind the removal of PP in stormwater wetlands, since the diameter of particles influences the settling velocity and the amount of sorbed P on a particle. In this paper, we present a novel method to estimate PP, where we measure and count individual particles in stormwater and use the total surface area as a proxy for PP. Our results show a strong relationship between total particle surface area and PP, which we use to put forth a simple mechanistic model of PP removal via gravitational settling of individual mineral particles, based on a continuous particle size distribution. This information can help improve the design of stormwater Best management practices to reduce PP loading in both urban and agricultural watersheds.     

Quantification of ionophores in aged poultry litter using liquid chromatography tandem mass spectrometry

Veterinary anticoccidials, biochemically known as ionophores, are widely used in poultry feed at therapeutic levels to treat Coccidiosis and at sub-therapeutic levels for growth- promotion. Commonly used ionophores in the US poultry industry are monensin, salinomycin, lasalocid and narasin. There is an increasing concern regarding the persistence of these anticoccidials in the environment. However, little attention has been directed to methods development for quantitatively measuring ionophores in complex environmental matrices such as poultry litters that are land applied. Here, we describe a rapid and sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS)-based method developed for simultaneous quantification of monensin, lasalocid, salinomycin, and narasin in aged poultry litter samples. Results show significant level of monensin (97.8 ± 3.2 μg kg^?1), lasalocid (19.2 ± 6.6 μg kg^?1), salinomycin (70 ± 2.7 μg kg^?1) and narasin (57.3 ± 2.6 μg kg^?1) in poultry litter stored for over three years at < 5°C. Our findings indicate that even after several years of unmanaged storage of poultry litter, ionophores may continue to persist in this matrix, raising the possibility of prolonged release into the environment.     

Lead and zinc bioavailability to Eisenia fetida after phosphorus amendment to repository soils

Four phosphorus forms were investigated as potential soil amendments to decrease the bioavailability of Pb and Zn in two repository soils to the earthworm, Eisenia fetida. Treatments were evaluated by examining differences in bioaccumulation factors between amended and non-amended soils. Triple super phosphate at 5000 mg P/kg decreased both Pb and Zn bioavailability in both soils. Rock phosphate at 5000 mg P/kg decreased Zn bioavailability, but not Pb bioavailability in both repository soils. Monocalcium phosphate and tricalcium phosphate at 5000 mg P/kg did not significantly decrease Pb or Zn bioavailability to earthworms in either repository soil. In order to optimize phosphorus amendments, additional phosphorus (up to 15,000 mg P/kg) and lowered pH were used in a series of tests. The combination of lowering the pH below 6.0 and increasing phosphorus concentrations caused complete mortality in all triple super phosphate amended soils and partial mortality in the highest rock phosphate amended soils. Results indicate that triple super phosphate and rock phosphate are viable soil amendments, but care should be taken when optimizing amendment quantity and pH so that adverse environmental effects are not a by-product.     

Preliminary economic analysis of poultry litter gasification option with a simple transportation model

Several environmental issues are related to the disposal of poultry litter. In an effort to provide a more environmentally friendly alternative than landfill disposal or spreading as a soil amendment, work has been carried out previously at the University of Tennessee Space Institute (UTSI). This past UTSI work was concentrated on developing a catalytic steam gasification concept to produce energy from poultry litter. In the past UTSI studies, preliminary design and economics for a stationary, centralized gasification plant capable of processing approximately 100 ton/day of poultry litter were developed. However, in this preliminary design the economic impact of transporting litter to a centralized gasification plant location was not addressed. To determine the preliminary impact of transporting the poultry litter on the overall economics of this energy conversion plant design, a simple transportation model was developed. This model was used in conjunction with the earlier plant design prepared at UTSI to determine the economic feasibility of a centralized, stationary poultry litter gasification plant. To do so, major variables such as traveling distance, plant feed rate (or capacity), fluctuations in the sales price of the product gas (that means value of the energy), population density of poultry farms, impact of tipping fees, and cost of litter were varied. The study showed that for plant with a capacity of 1000 ton/day to be able to withstand several changes in economic conditions and sustain itself, the poultry farm density would need to be approximately 0.3 houses/mi2. Smaller plants would need either a higher energy price or some kind of subsidy to be economically feasible.     

改性方解石的除磷能力研究

选用颗粒方解石,对其表面进行改性,便于磷在其表面的吸附、结晶、沉淀,形成永久性固态磷,加速磷的自然沉淀过程。考察了改性的最佳条件和改性方解石除磷的影响因素。结果表明,方解石的最佳改性条件:改性液TP、Ca2+、HCO-3分别为93.00、120.00、244.00 mg/L,浸泡时间2d;改性方解石具有持续的除磷能力,在实验前76h的平均除磷速率为0.053 0mg/(g·d),而稳定阶段的除磷速率为0.021 4mg/(g·d);待处理水样的Ca2+浓度对改性方解石的除磷效果有较大影响,Ca2+为120.00mg/L时除磷效果最好,碱度对除磷效果的影响很小;pH≤7.30,投加改性方解石系统中磷的去除以改性方解石表面Ca-P结晶为主,而当pH≥8.15时,溶液中发生Ca-P沉淀,而Ca-P结晶逐步减少;水温对改性方解石的除磷效果具有显著影响。     

Quantification of ionophores in aged poultry litter using liquid chromatography tandem mass spectrometry

Veterinary anticoccidials, biochemically known as ionophores, are widely used in poultry feed at therapeutic levels to treat Coccidiosis and at sub-therapeutic levels for growth- promotion. Commonly used ionophores in the US poultry industry are monensin, salinomycin, lasalocid and narasin. There is an increasing concern regarding the persistence of these anticoccidials in the environment. However, little attention has been directed to methods development for quantitatively measuring ionophores in complex environmental matrices such as poultry litters that are land applied. Here, we describe a rapid and sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS)-based method developed for simultaneous quantification of monensin, lasalocid, salinomycin, and narasin in aged poultry litter samples. Results show significant level of monensin (97.8 ± 3.2?μg kg(-1)), lasalocid (19.2 ± 6.6?μg kg(-1)), salinomycin (70 ± 2.7?μg kg(-1)) and narasin (57.3 ± 2.6?μg kg(-1)) in poultry litter stored for over three years at < 5°C. Our findings indicate that even after several years of unmanaged storage of poultry litter, ionophores may continue to persist in this matrix, raising the possibility of prolonged release into the environment.