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1.
This paper presents a field study conducted in northwest Turkey and characterizes the NH3 concentration and emission measured in summer season from three chicken farms. The influence of environmental conditions on NH3 concentration and emission was also investigated in this study. Ammonia concentration, temperature, relative humidity and airflow rate were continuously recorded for four sequential days. The environmental conditions were measured using a multifunction temperature and humidity‐meter with a hot wire probe. Portable multiple gas detectors with electro‐chemical sensors were used to measure NH3 concentration. The NH3 emission rates for houses were calculated by multiplying simultaneously measured NH3 concentrations and air flow rates. The average daily mean (ADM) house concentrations of house 1 (H1), house 2 (H2), and house 3 (H3) were measured as 4.43, 3.71, and 6.20 ppm, respectively. NH3 concentration was inversely proportional to temperature (r = ?0.279), relative humidity (r = ?0.063) and airflow rate (r = ?0.554) for all monitored houses. The ADM house NH3 emission was 135 g/(h house) for H1, 255 g/(h house) for H2, and 117 g/(h house) for H3. The combined average emission rate in this study (0.26 g/(d bird)) was lower than the emission rate measured in chicken farms in the USA. However, our results were comparable to rates calculated in European studies because house design, ventilation system and bird diet applied in Turkish chicken farms are very similar to those employed in European countries. The NH3 emissions were significantly correlated to NH3 concentrations (r = 0.45, p ≤ 0.001) and airflow rates (r = 0.97, p ≤ 0.001). A clear diurnal pattern was obtained for NH3 concentrations rather than NH3 emissions at the end of the study. 相似文献
2.
Ammonium Ion, Humic Materials, and Trihalomethane Potential in Northeastern Kansas Ground Waters 总被引：1，自引：0，他引：1
Glacial buried-valley aquifers serve as primary sources of potable ground water in northeastern Kansas. A long known problem, however, is that a large percentage of well waters in this region exceed the U.S. Environmental Protection Agency (EPA) limits for nitrate (NO−3). A detailed study of the hydrogeology and water quality of the buried valleys has confirmed the nitrate problem and led to a recognition that some well waters with low ( 5 mg/l) NO−3 concentrations have anomalous ( 0.5 mg/l) ammonium ion (NH+4) levels, with an NH+4 range from <0.1 to 4.8 mg/l. The extractable NH+4 concentrations in related glacial sediments range up to approximately 75 mg/kg, and the amounts generally increase from an average of 2 mg/kg in the topsoil downward to bedrock. Migration of brines from subjacent Permian or Pennsylvanian bedrock into the unconsolidated sediments locally may cause desorption of NH+4 and an increase in its levels in the associated ground waters. Numerous test holes drilled in the study area showed a black scum on the fluid and cuttings, which may be from buried humic materials. Recently measured total organic carbon (TOC) contents of the ground waters confirm a significant level in some areas, with a range from 0.1 to 2.4 mg/l as C. Chlorination of water with dissolved organics may lead to production of halogenated compounds. Two public-water-supply well waters contained total trihalomethane (TTHM) levels close to the maximum contaminant level (MCL) of 100 /μg/l in chlorinated samples quenched after one week. The presence of NH+4 inhibits the formation of THMs, but it also can give rise to odor and taste problems in the finished water. The inhibition of THM formation by NH+4 is achieved by reactions which compete with the organics for combination with chlorine. These reactions make maintaining appropriate chlorine residuals difficult and also may lead to production of undesirable side products. Present efforts to evaluate the regional water-quality problems are focused in Nemaha County, Kansas. 相似文献
3.
The differential-pulse polarography (DPP) and the stripping voltametry (SV) are investigated in detail with respect to their suitability for the quantitative detection of individual traces of heavy metals in sewage sludge. The results are checked on the basis of AAS analyses and by the standard-addition method. From the hydrochloric-acid extracts of fused sludge samples down to 1 μg/l can be detected by the SV, whereas the DPP reaches a sensitivity of 100 μg/l. The following basic electrolytes are used: Zn: 2 … 3 mol/l H3PO4; Cu: 0.4 mol/l K2CO3, 0.2 mol/l Na-K-tartrate, 0.1 mol/l HCl; Ni: 1 mol/l NH4OH, 1 mol/l NH4Cl, 25 ml/l triethylamine; Pb and Cd: 0.1 … 0.2 mol/l HCl. 相似文献
4.
Sediment and seawater samples were taken in a sewage affected channel in Blanca Bay, Argentina. Protein content, ‘humic substances’ and silt-clay percentage were evaluated in the sediments; NH4+, PO43? and ‘dissolved organic matter’ in seawater. A highly significant correlation (r=0.747, n=59) was obtained for the relation between protein and % silt-clay. The ‘humic substances’ distribution depends more on the distance from the outfall than does the protein content, probably because of the important relation of the latter with the sediment particle size. The dissolved components showed a dilution pattern similar to that of a contaminant plume in a moving water mass, reaching normal values at 1700 m from the outfall. 相似文献
5.
The organic composition and organic‐inorganic interaction in paper mill sludge (PS) solvent extracts (hexane, ethyl acetate, acetone and ethanol) and humic fractions, humic acid (HA) and humin (HU) were studied by electron paramagnetic resonance spectroscopy (EPR), proton and carbon‐13 nuclear magnetic resonance spectroscopy (1H NMR; 13C NMR), Fourier‐transformed infrared spectroscopy (FTIR), and ultraviolet‐visible spectroscopy (UV‐vis). The strategy of fractionating the PS, sequentially, with organic solvents of increasing polarity is a reliable analytical procedure for humic substance sample separation because it results in more purified fractions. FTIR, 1H NMR and 13C NMR results showed that hexane extract consisted mainly of aliphatic hydrocarbon structures. Their contents in the extracts decreased as the polarity of the extracting solvent increased and the content of oxygen functional groups increased. Carboxylic and carboxylate functional groups were found in the acetone extract, and ester and ether functions were predominantly found in the ethanol extract. EPR spectra revealed some Fe3+ complexes with rhombic structure (g1 = 4.3; g2 = 9.0) in the humic fractions and in all solvent extracts, except hexane. Quasi‐octahedral Fe3+ complexes (g = 2.3; ΔHpp ≤ 400 G) were found in the HU fraction and in the acetone extract. The organic free radical content in the HA fraction was higher than the non‐fractionated PS sample and HU fraction. 相似文献
6.
Soodabeh Khalili Ali Asghar Ghoreyshi Mohsen Jahanshahi Kasra Pirzadeh 《洁净——土壤、空气、水》2013,41(10):939-948
In this study, crude multi‐walled carbon nanotubes (MWCNT) was functionalized by a two‐step process; first using strong mixed acids (H2SO4/HNO3) and then treatment with 1,3‐phenylenediamine (mPDA). The equilibrium adsorption of CO2 on pristine MWCNT and amine functionalized MWCNT (MWCNT‐NH2) were investigated. Experiments were preformed via application of volumetric method in a dual sorption vessel at temperature range of 298–318 K and pressures up to 40 bars. The results obtained indicated that the equilibrium uptake of CO2 increased after functionalizing of MWCNT. The increase in CO2 capture by MWCNT‐NH2 was attributed to the existence of great affinity between CO2 molecules and amine sites on this adsorbent at low pressures. The experimental data were analyzed by means of Freundlich and Langmuir adsorption isotherm models. The data obtained revealed a fast kinetics for the adsorption of CO2 in which most of adsorption occurred at initial period of adsorption experiments. This renders MWCNT as a suitable adsorbent for practical applications. Values of isosteric heat of adsorption were evaluated based on Clausius–Clapeyron equation. The results demonstrated that both chemisorption and physisorption played important role in CO2 adsorption on MWCNT‐NH2, whereas the physisorption process was dominant for CO2 adsorption on MWCNT. 相似文献
7.
The water quality guideline trigger value for ammonia in estuarine and marine waters has been revised with the addition of 38 new results to the data set of 21 used in earlier guideline derivations. Using species sensitivity distributions, a new trigger value of 460 μg total NH3-N/L was derived for slightly to moderately disturbed systems (95% protection concentration, PC95), with a value of 160 μg total NH3-N/L applying to waters of high conservation value (PC99). For sediment pore waters, a guideline trigger value of 3.9 mg total NH3-N/L, derived from the 80th percentile of background data from Sydney Harbour, is recommended. This value is likely to be exceeded in degraded sediments subject to dredging; however, ocean disposal of such sediments results in rapid decreases in porewater ammonia and a guideline trigger value for dissolved ammonia during disposal of dredged sediments of 1550 μg total NH3-N/L is proposed. 相似文献
8.
On a bench scale the treatment of electroplating effluents (ZnCl2, NiCl2, NH4Cl, NH3 and two polyether compounds) with Wofatit CA20 is investigated. If the capacity of the resin is utilized to a high degree for the heavy metal ions, the organic matter remains in the filtrate. The results are discussed with regard to the recovery and waste-disposal technology on a large scale. 相似文献
9.
After treatment of the anion exchanger resins from several manufacturers with FeCl3 or CuSO4 their capacity to take up thiocyanate ions increases by the factor 2 … 3. By regeneration with diluted sulphuric acid or hydrochloric acid after precipitation of the ferric or cupric hydroxide a thiocyanate solution of 10 and 15 g/l, respectively, is obtained, which can be reused. The hydroxides dissolved in acid are used for the treatment of the ion exchanger. The process is proposed for the regenerating of wastewaters containing thiocyanate. 相似文献
10.
Determination of Partition Coefficients for Selected PAHs between Water and Dissolved Organic Matter
The fate and transport of highly hydrophobic chemicals are affected by the partitioning between water and dissolved organic carbon. Large variation in the partition coefficient (KDOCw) is often found, due to the selection of model organic matter or potential experimental artifacts. To investigate the roles of the type of organic matter on the partitioning of highly hydrophobic compounds, the partition coefficients of eight selected polycyclic aromatic hydrocarbons (PAHs), with 3–6 aromatic rings, were determined using a passive dosing/extraction method between water and model dissolved organic matter (humic acid, fulvic acid, sodium dodecyl sulfate micelle (SDS), and 2‐hydroxypropyl‐β‐cyclodextrin). Although the KDOCw values for 3–4 ring PAHs in this study were close to those reported in the literature, experimental KDOCw values between Aldrich humic acid (AHA) and water were higher than values reported in the literature for 5–6 ring PAHs. The KDOCw values were highest for AHA, followed by SDS and Suwannee river fulvic acid (SFA). The slopes of the linear regression between log KDOCw and log Kow were 1.23 (± 0.13), 0.82 (± 0.09), and 0.59 (± 0.13) for AHA, SDS, and SFA, respectively. The differences in the KDOCw values between AHA and the other organic matter (SDS, SFA, and CD) increased with increasing hydrophobicity of the PAHs, showing that the sorption of highly hydrophobic chemicals to the humic acid fraction may be important in the presence of mixed organic matter. 相似文献
11.
湖泊生态系统作为自然界重要的碳库,光照强度的变化对于湖泊的碳循环过程可能产生重要的影响.以云南老君山高山湖泊天才湖周边土壤中的腐殖酸作为外源溶解性有机物（DOM）的代表物,通过腐殖酸模拟光降解实验,考察光照强度对外源DOM光降解过程的影响.研究结果表明：腐殖酸光吸收系数a440、465 nm和665 nm波长处吸光度比值E4/E6的下降幅度均为：对照组 < 20 W光照组 < 40 W光照组,a440、E4/E6和光谱斜率SR显著相关,表明紫外辐射使得腐殖酸溶液浓度降低、相对分子量下降,且光照强度越强,腐殖酸的光降解程度越大.通过EEM-PARAFAC模型识别出光降解过程中腐殖酸溶液中含有5种荧光组分：UV类腐殖质（C1）、UVA类腐殖质（C2）、类色氨酸（C3）、UVC类腐殖质（C4）和类络氨酸（C5）.40 W光照组中4种荧光组分的降解程度与降解速率均大于20 W光照组,降解程度均为：C4 > C3 > C2 > C1,降解速率为C2 > C4 > C3 > C1,说明不同的荧光组分对光照强度的响应不同.该研究有助于阐明外源DOM的光降解途径与归趋. 相似文献
12.
By diluting a boggy water there is produced water with a COD-Mn of 3.4 … 10.6 mg/l O2 which is due only to humic substances. The water is mixed with 2.5 … 12.9 mg/l Cl2 at pH-values of 5.2 … 8.5 and incubated for 24 h at 20°C. CHCl3 concentrations of 38 … 480 μg/l were found by the subsequent gas-chromatographic determination. The production of chloroform can be calculated by means of a quadratic polynomial in dependence on COD-Mn, chlorine concentration and pH-value. 相似文献
13.
Humic acid plays an important role in the distribution of heavy metals in the environment. The aims of this study were conducted to evaluate the spectroscopic characteristics and aluminum (Al) adsorption of humic acids which were extracted from four composts. The functional groups were determined by Fourier transform infrared spectroscopy (FTIR) and solid‐state 13C nuclear magnetic resonance spectroscopy (13C‐NMR). The results showed that the aromatic groups were all found in the humic acids of the four composts, and the surface of humic acids included carboxylic group, hydroxylic group, and amino group. The experiment of Al adsorption was described by Freundlich equation. It showed that the adsorption of Al by humic acid from compost of cattle manure was higher, but that from the compost of pig manure, lemon manure, tea manure in equal preparation was lower. The adsorptive behavior was different due to the interaction by functional groups ( OH and COOH) with Al. These results can describe the fate and transportation of Al in the soil of different organic fertilizer. 相似文献
14.
Ultrafiltration (UF) can remove natural organic matter (NOM) effectively. Moreover, chlorine dioxide (ClO2) has been an alternative disinfectant as it forms fewer disinfection by‐products with NOM than chlorination does. Therefore, combining ClO2 with UF may improve conventional purification processes. In this study, feed water containing humic acid with 4.07 mg/L total organic carbon (TOC) was dosed directly with various amounts of ClO2 (0, 2, 5, 10, and 15 mg/L) before being filtered through a 5‐kDa UF membrane. With a low dose (2 mg/L ClO2), UF removed humic acid effectively, as TOC was not detected in the permeate, and the permeate flux increased to about 80% of the initial permeate flux by cross flow. Moreover, the concentrations of ClO, ClO, and trihalomethanes in the permeate were below the United States Environmental Protection Agency guidelines. 相似文献
15.
为了研究太湖底栖动物优势种类——霍甫水丝蚓(Limnodrilus hoffmeisteri)对于湖泊富营养化的影响,以温度和密度为模拟控制条件,对太湖霍甫水丝蚓进行营养盐释放的室内控制实验,研究温度和密度的变化对霍甫水丝蚓NH_4~+-N和PO_4~(3-)-P释放率的影响,根据霍甫水丝蚓铵态氮(NH_4~+-N)和磷酸盐(PO_4~(3-)-P)释放率与温度的关系方程,结合太湖霍甫水丝蚓2007-2010年的生物量估算其对太湖水体氮磷的潜在贡献.结果表明,随温度升高太湖霍甫水丝蚓NH_4~+-N和PO_4~(3-)-P的释放率均呈现逐渐升高的趋势,而密度变化对霍甫水丝蚓NH_4~+-N和PO_4~(3-)-P释放率的影响均不显著,太湖霍甫水丝蚓NH_4~+-N和PO_4~(3-)-P年平均释放量分别为1925.5和210.0 t,分别可达到全太湖沉积物-水界面NH_4~+-N和PO_4~(3-)-P的年净通量的19.3%和23.3%,表明霍甫水丝蚓的营养盐释放对于湖泊生物地化循环和湖泊富营养化具有显著的影响. 相似文献
16.
由于严重的水体富营养化,太湖长期暴发蓝藻水华,这些蓝藻在代谢及消亡过程中大量释放包括腐植酸在内的有机物,不仅影响供水水质,并且进一步加重了水华程度.以太湖水华优势藻种——水华微囊藻(Microcystis flos-aquae T34)为研究对象,对藻株生长周期中的藻细胞、浮游细菌进行计数,并使用TOC仪与三维荧光光谱对培养液中提取的腐殖酸进行定量与定性分析,探究水华微囊藻在生长过程中藻细胞密度、浮游细菌密度与腐殖酸浓度的变化规律.结果表明,培养液中腐殖酸浓度的变化趋势与细菌数量变化趋势一致,但与细菌数量曲线拐点相比,腐殖酸浓度曲线拐点出现两周的延迟.腐殖酸产量在藻细胞对数期较低,当水华微囊藻进入稳定期与衰亡期后,腐殖酸大量产生,其浓度迅速增加,最高可达到28.6 mg/L.根据三维荧光光谱分析,水华微囊藻所产生的腐殖酸特征峰出现在(235~245 nm)/(380~425 nm),属于类富里酸荧光峰.本研究初步探究蓝藻与水体腐殖酸之间的关系,为水体腐殖酸来源的研究提供了新的思路. 相似文献
17.
Yu Chen Yan‐peng Mao Hai‐song Zhu Jing‐yi Cheng Xiang‐li Long Wei‐kang Yuan 《洁净——土壤、空气、水》2010,38(7):601-607
The wet ammonia (NH3) desulfurization process can be retrofitted to remove nitric oxide (NO) and sulfur dioxide (SO2) simultaneously by adding soluble cobalt(II) salt into the aqueous ammonia solution. Activated carbon is used as a catalyst to regenerate hexaminecobalt(II), Co(NH3), so that NO removal efficiency can be maintained at a high level for a long time. In this study, the catalytic performance of pitch‐based spherical activated carbon (PBSAC) in the simultaneous removal of NO and SO2 with this wet ammonia scrubbing process has been studied systematically. Experiments have been performed in a batch stirred cell to test the catalytic characteristics of PBSAC in the catalytic reduction of hexaminecobalt(III), Co(NH3). The experimental results show that PBSAC is a much better catalyst in the catalytic reduction of Co(NH3) than palm shell activated carbon (PSAC). The Co(NH3) reduction reaction rate increases with PBSAC when the PBSAC dose is below 7.5 g/L. The Co(NH3) reduction rate increases with its initial concentration. Best Co(NH3) conversion is gained at a pH range of 2.0–6.0. A high temperature is favorable to such reaction. The intrinsic activation energy of 51.00 kJ/mol for the Co(NH3) reduction catalyzed by PBSAC has been obtained. The experiments manifest that the simultaneous elimination of NO and SO2 by the hexaminecobalt solution coupled with catalytic regeneration of hexaminecobalt(II) can maintain a NO removal efficiency of 90% for a long time. 相似文献
18.
Many large rivers worldwide are enriched with high levels of suspended solids (SS), which are known to be hotspots of many nitrogen (N) transformation processes (e.g., denitrification, nitrification). However, the influence of SS on microbial ammonium (NH4+) recycling remains unclear. Water column NH4+ regeneration rates (REGs) and potential uptake rates (Upots) as well as community biological NH4+ demand (CBAD) was measured in the river-estuary continuum of the third longest river in the world—Yangtze River, which has dramatic SS gradients. We found that REGs, Upots, and CBAD all increased downriver, with higher REGs, Upots, and CBAD in the estuary than in the river sections. The regeneration and uptake of NH4+ were nearly balanced in the river sections, while the positive CBAD in the estuary indicated obvious NH4+ demand of microbes. Concentrations of SS, which also control the content of chemical oxygen demand and particulate N, were the main factor influencing NH4+ recycling rates and CBAD. SS-induced regenerated NH4+ in the river-estuary continuum of Yangtze River was estimated to be 11.02 × 108 kg N yr−1 and accounted for about 14% of total N inputs, suggesting that regenerated NH4+ is an important N source for microbes and may influence nutrient dynamics in lower coasts. To our knowledge, this is the first study to report NH4+ recycling in Yangtze River with an emphasis on its influencing factors and contribution to N budgets. 相似文献
19.
基于洱海水生态特征的流域最大日负荷总量控制 总被引：1，自引：1，他引：0
基于洱海水生态历史数据及现状资料,采用概率密度分布曲线法及水生生物基准相结合的方式计算洱海总氮(TN)、总磷(TP)、高锰酸盐指数(COD_(Mn))和氨氮(NH_3-N)的控制目标,目标值分别为0.36、0.026、4和0.28 mg/L.再根据该水质目标,得到洱海的最大日负荷(TMDL)总量.TMDL总量采用线性规划法计算,其中污染物响应系数矩阵通过MIKE 21二维水质模型计算所得.安全容余(MOS)则通过一阶误差分析法确定.经过一系列的计算,最终确定洱海的TMDL总量控制计划.计算结果表明,洱海TN、TP、COD_(Mn)和NH_3-N的TMDL总量分别为2005.989、149.671、19258.844和1348.119 kg/d,其MOS所占比例分别为6.152%、5.570%、4.380%和5.021%,表明洱海农业面源污染为该流域主要的污染形式,其允许最大排放量约占全部允许排放量的90%左右. 相似文献
20.
To improve quantitative understanding of mixed‐land‐use impacts on nutrient yields, a nested‐scale experimental watershed study design (n = 5) was applied in a 303(d), clean water act impaired urbanizing watershed of the lower Missouri River Basin, USA. From 2010 to 2013, water samples (n = 858 sample days per site) were analysed for total inorganic nitrogen (TIN‐N), nitrite (NO2–N) nitrate (NO3–N), ammonia (NH3–N), and total phosphorus (TP‐P). Annual, seasonal, and monthly flow‐weighted concentrations (FWCs) and nutrient yields were estimated. Mean nutrient concentrations were highest where agricultural land use comprised 58% of the drainage area (NH3 = 0.111 mg/l; NO2 = 0.045 mg/l; NO3 = 0.684 mg/l, TIN = 0.840 mg/l; TP = 0.127 mg/l). Average TP‐P increased by 15% with 20% increased urban land use area. Highly variable annual precipitation was observed during the study with highest nutrient yields during 2010 (record setting wet year) and lowest nutrient yields during 2012 (extreme drought year). Annual TIN‐N and TP‐P yields exceeded 10.3 and 2.04 kg ha?1 yr?1 from the agricultural dominated headwaters. Mean annual NH3–N, NO2–N, NO3–N, TIN‐N, and TP‐P yields were 0.742, 0.400, 4.24, 5.38, and 0.979 kg ha?1 yr?1, respectively near the watershed outlet. Precipitation accounted for the majority of the explained variance in nutrient yields (R2 values from 0.68 to 0.85). Nutrient yields were also dependent on annual precipitation of the preceding year (R2 values from 0.87 to 0.91) thus enforcing the great complexity of variable mixed‐land‐use mediated source‐sink nutrient yield relationships. Study results better inform land managers and best management practices designed to mitigate nutrient pollution issues in mixed‐land‐use freshwater ecosystems. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献