首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
离子色谱法同时测定铀矿浸出液中的阳离子   总被引：1，自引：0，他引：1  
对铬铁矿中亚铁的测定方法进行了探讨。首先对已有方法进行了验证和筛选,然后对Li2SO4助熔剂的助溶作用及其反应机理进行了研究,从而推荐了H2SO4-H3PO4-V2O5-V(Ⅳ)-Li2SO4和H2SO4-H3PO4-Ce(SO4)2-Li2SO4两种改进型的溶剂体系用于铬铁矿试样中亚铁的测定,所得结果具有良好的重现性。  相似文献   

2.
Two sets of lab-scale sequencing batch reactors (SBR), i.e., control SBR and SBR using zeolite as carrier (zeo-SBR), were applied to assess nitrogen removal efficiency. The test results revealed that zeolite powder added in SBR could improve its performance. Due to the combination of zeolite adsorption for NH4 +–N and enhanced simultaneous nitrification and de-nitrification (SND), a higher removal ratio of ammonia nitrogen in wastewater was observed in the test reactor, and the introduction of zeolite powder was helpful to inhabit sludge bulging comparing with the control SBR, in other words, activated sludge immobilized by zeolite powder could remove NH4 +–N, COD, and PO4 significantly in a shorter cycle time. Applied two hydraulic retention times (HRTs) showed that the nitrogen and phosphorus removal could be improved while adapting to load variations.  相似文献   

3.
《Applied Geochemistry》2004,19(9):1495-1503
Compositional data from published sources, environmental monitoring and new analyses demonstrate that for a wide range of water types (oilfield water, coal mine water, landfill leachate) NH4+ is present in amounts up to 2200 mg/L. Oilfield waters from Alberta, Canada contain 1–1000 mg/L NH4+, coal mine water (UK) surface discharges 1–45 mg/L NH4+, and landfill leachates (UK) up to 2200 mg/L NH4+. Ammonium contents generally show a positive correlation with K, and increase with increasing salinity. Geochemical modelling of sufficiently complete data using SOLMINEQ88 demonstrates that NH4+ activities vary systematically, and are consistent with a mineralogical control. Sodium–K exchange divides the entire sample suite into at least 4 groups, controlled by reaction temperature and reaction with either albite/K-feldspar or illitic clay minerals. In contrast, comparison of NH4+ and K divides the sample suite into 2 groups. On the basis of geological setting, these correspond to K–NH4+ exchange involving illitic (illite-muscovite) clays (and possibly feldspars) for samples from natural sources, and to exchange involving smectitic clays for samples from landfill sites. This study demonstrates the importance of NH4+ as a constituent of natural groundwaters, requiring that this reservoir of N is taken into account in detailed discussion of hydrological components of the N cycle.  相似文献   

4.
The use of natural zeolites for environmental applications is gaining new research interests mainly due to their properties and significant worldwide occurrence. The present work describes the characterization of a natural Chilean zeolite and the results as adsorbent for ammonia from aqueous solutions. The zeolitic-rich tuff sample, mainly composed of clinoptilolite and mordenite, consisted of 13 μm mean volumetric particle diameter, 55 m2 g−1 (methylene blue adsorption) and 177 m2 g−1 (nitrogen adsorption) of specific surface area. Particles were negatively charged over a broad pH range (with or without ammonia) and 1.02 meq NH4+ g−1 cation-exchange capacity. The ammonia removal appears to proceed through ion-exchange and rapid kinetics (rate constant of 0.3 min−1) at neutral pH value, with removal capacities up to 0.68 meq NH4+ g−1. The Langmuir isotherm model provided excellent equilibrium data fitting (R2=0.97). Results indicate a significant potential for the Chilean natural zeolite as an adsorbent/ion-exchange material for wastewater treatment and water reuse applications.  相似文献   

5.
The radioactive fission product, 137Cs, has been observed to mobilize from bottom sediments of two South Carolina reservoirs during summer thermal stratification and hypolimnetic anoxia. Mobilization is attributed to ion-exchange displacement of 137Cs from sediments by cations such as NH+4, Fe+2 and Mn+2 released under anaerobic conditions.Three types of 137Cs binding sites to sediment clay minerals are identified: 1) surface and planar sites from which 137Cs is generally exchangeable by all cations studied (Na+, NH+4, H+, Cs+, Ca+2, Mg+2, Fe+2, and Mn+2); 2) wedge sites where 137Cs exchange is sterically limited to cations of similar size and charge (NH+4, Cs+, K+, and perhaps H3O+); 3) interlayer sites from which 137Cs is not readily exchanged. More than 15 years after final 137Cs inputs, the reservoir sediments we studied showed the following percentage distribution of sites: 2 to 9% surface sites, 6 to 13% wedge sites, and 78 to 85% interlayer sites. In contrast, lake and stream sediments near Oak Ridge, Tennessee receiving 137Cs inputs more than 20 years earlier had greater than 99% of their 137Cs associated with non-exchangeable interlayer sites. The difference is attributed to the paucity in the South Carolina sediments of weathered micaceous clay minerals with their abundant interlayer sites. Such interlayer deficient clays are dominant in the Atlantic and Gulf coastal plains of the United States and elsewhere. This suggests that 137Cs will be physically and chemically more mobile in such areas as well as more biologically available. Mobility will be enhanced in regimes where cation inputs favoring 137Cs exchange occur. Subsurface waste disposal sites where anaerobic conditions develop with NH+4 production and Fe+2 and Mn+2 release might be such a regime.  相似文献   

6.
The results of experimental studies of ion exchange properties of Co-bearing ferromanganese crusts in the Magellan Seamounts (Pacific Ocean) are discussed. Maximum reactivity in reactions with the participation of manganese minerals (Fe-vernadite, vernadite) is typical of Na+, K+, and Ca2+ cations, whereas minimum activity is recorded for cations Pb2+ and Co2+. The exchange complex of ore minerals in crusts is composed of Na+, K+, Ca2+, Mg2+, and Mn2+ cations. The exchange capacity of manganese minerals increases from the alkali metal cations to rare and heavy metal cations. Peculiarities of the affiliation of Co2+, Mn2+, and Mg2+ cations in manganese minerals of crusts are discussed. In manganese minerals, Co occurs as Co2+ and Co3+ cations. Metal cations in manganese minerals occur in different chemical forms: sorbed (Na+, K+, Ca2+, Mn2+, Co2+, Cu2+, Zn2+, Cd2+, and Pb2+); sorbed and chemically bound (Mg2+, Ni2+, Y3+, La3+, and Mo6+); and only chemically bound (Co3+). It is shown that the age of crust, its preservation time in the air-dry state, and type of host substrate do not affect the ion exchange indicators of manganese minerals. It has been established that alkali metal cations are characterized by completely reversible equivalent sorption, whereas heavy metal cations are sorbed by a complex mechanism: equivalent ion exchange for all metal cations; superequivalent, partly reversible sorption for Ba2+, Pb2+, Co2+, and Cu2+ cations, relative to exchange cations of manganese minerals. The obtained results refine the role of ion exchange processes during the hydrogenic formation of Co-bearing ferromanganese crusts.  相似文献   

7.
Chemical analyses of pore waters from recent marine carbonate sediments, Devil's Hole, Harrington Sound, Bermuda, have been obtained at intervals over a four year period. Interstitial waters were systematically analyzed for pH, titration alkalinity, dissolved sulfides, NH4+, Ca2+, Mg2+ and Na+ or Cl?. Additional analyses on some cores included SO42?, PO43?, dissolved CH4 and N2, and C:N:H ratios in the detrital organic material. The following general trends with depth (to ～ 1 m) are observed: (1) major cations show little or no change; (2) pH decreases; (3) alkalinity, sulfides, NH4+ and PO43? increase; (4) dissolved CH4 is consistently low. The chemical changes with depth can be modelled theoretically and are consistent with experimental data.Significant seasonal changes in pore water chemistry are observed. The data suggest an annual exchange between the pore waters (to a depth of ～ 1 m) and the overlying water of Harrington Sound; the exchange occurs between August and January. The nutrient flux out of the sediments during this process may be a major factor in the plankton ecology of Harrington Sound.  相似文献   

8.
It is shown that the reaction ability of metal cations of ore minerals in Fe–Mn crusts of the Marcus Wake Rise increases in the following manner: (Co2+ < Cu2+ < Ni2+) < (Mg2+ < Mn2+ < K+ ≈ Ca2+ ≈ Na+). The composition of the exchange complex of the ore minerals is constant and includes these metal cations. Ca2+ and Na+ are major contributors to the exchange capacity of the ore minerals. The capacity of the ore minerals by cations of alkali and base metals is 0.43–0.60 and 2.08–2.70 mg-equiv/g, respectively. The exchange capacity of the ore minerals by cations of base metals increases linearly with the increase in the MnO2 content of the crust and does not depend on the geographical locations of the Marcus Wake guyots.  相似文献   

9.
 The exchange and release properties of the natural phillipsite tuff from the Aritain area in Jordan were evaluated by studying the exchange properties of this natural zeolite in the NH4 +–Na+ system. Exchange isotherms at 18, 35, and 50  °C showed that phillipsite exchanged NH4 + preferably over Na+ at all temperatures. However, the selectivity coefficient for NH4 + decreased with decreasing temperature. The release of NH4 + from phillipsite saturated with ammonium sulfate took place in two stages characterized by different SO4 2– : NH4 + ratios. Aritain phillipsite from NE Jordan could be processed and used as NH4 + slow-release fertilizers. The use of NH4 +-phillipsite tuff offers an option to the widely used soluble NH4-fertilizers in agciculture to avoid environmental problems associated with nitrogen contamination of surface water and groundwater. Received: 19 December 1996 · Accepted: 13 May 1997  相似文献   

10.
A combined ABR–MBR process consisting of an anaerobic baffled reactor (ABR) combined with an aerobic membrane bioreactor (MBR) treating municipal wastewater was investigated at controlled pH range 6.5–8.5 and at constant temperature 25 ± 1 °C. Total nitrogen (TN), ammonia (NH4 +–N), total phosphorus (TP), and chemical oxygen demand (COD) removal performances were evaluated by analyzing the mechanism for efficient nutrient removal. The results showed that the average removal rates of COD, NH4 +–N, TN, and TP reached 93, 99, 79, and 92 %, respectively, corresponding with the COD, NH4 +–N, TN, and TP effluent of 24 (18–31), 0.4 (0–0.8), 10.6 (8.8–12.9), and 0.31 (0.1–0.5) mg/L under the operational condition of hydraulic retention time (HRT) 7.5 h, recycle ratio 200 %, and dissolved oxygen 3 mg/L. The MBR enhanced NH4 +–N, TN, and TP removal rates of 13, 10, and 18 %, respectively, and the membrane retention reduced TP 0.17 mg/L. The process was able to maintain a stable performance with high-quality effluent. Analysis of the results by fluorescence in situ hybridization showed that the abundance of ammonia-oxidizing bacteria, nitrite-oxidizing bacteria, and phosphorus accumulating organisms as percentages of all bacteria in each compartment was stable. The enriched microorganisms in the system appear to be the main drivers of the process efficient for nutrient removal.  相似文献   

11.
Rainwater plays an important role in scavenging of aerosols and gases from atmosphere, and its chemistry helps to understand the relative contributions of atmospheric pollution sources. The present work is aimed to understand and explain the sources, seasonal patterns and the processes thereof affecting rainwater chemistry in an urban environment of Delhi, India. Rainwater samples (n = 111) collected throughout the year in New Delhi showed alkalinity in general. Eight rainwater samples, collected in late monsoon and winter season, had pH less than 5.6 indicating that Delhi continues to face the prospects of acid rain despite the introduction of compressed natural gas as the clean fuel in city transport. Organic acids could be the possible contributors of acidity in rainwater samples having the fractional acidity (FA) value of 0.174, which is greater than the annual average FA (0.011) and the (Ca2+ + Mg2+ + NH4 +)/(SO4 2? + NO3 ?) ration of more than one. Average acid neutralization factors of cations decrease in the order Ca2+ (1.01) > NH4 + (0.77) > Mg2+ (0.10). However, neutralization by Ca2+ dominates only in summer season as cation-rich dust is transported from the Great Indian Thar Desert to this region by strong summer S–SW winds, while NH4 + dominates in rainwater of other three sampling seasons. Identified dominant sources for soluble ions in rainwater are (1) non-silicate crustal source for carbonates and sulfates of Ca and Mg, (2) emissions from catalytic convertor-fitted vehicles and agriculture fields for NH3 and (3) mixed anthropogenic sources for SO4 2?, NO3 ? and Cl?. Rainwater chemistry showed significant seasonal variations. This could be due to the changes in relative proportions of natural and anthropogenic sources of soluble ions to rainwater. Dominance of anthropogenic sources over crustal sources can result in acidic rains, which can adversely affect the environment and human health in this region.  相似文献   

12.
为了研究祁连山大雪山地区大气PM2.5细粒子中可溶性无机离子组分的变化特征, 于2010年7月至2011年7月在祁连山冰川与生态环境综合观测站附近采集46个大气PM2.5的Telfon滤膜样品, 并应用离子色谱对可溶性离子进行了分析.结果显示: 所测样品的阴、 阳离子中, SO42-、 NO-3、 Ca2+和NH+4的质量浓度分别为1.54μg·m-3、 0.38μg·m-3、 0.73μg·m-3和0.22μg·m-3, 累计约占到水溶性离子总量的88%.可溶性离子浓度呈现出春夏季节明显高于秋冬季节的特征, 夏季的浓度最高, 其次是春季、 冬季和秋季. Cl-、 Ca2+、 Na+和Mg2+之间的相关性极高, SO42-和NO-3与大部分阳离子的相关性都很高, 说明大部分硫酸盐是来自于中亚沙尘源区的自然源, 而并非是通过人类活动造成的一次污染物通过二次反应过程得到的. NH+4仅与SO42-通过相关性检验说明, 该地区NH3主要中和了大气中硫酸并生成(NH4)2SO4.该地区的大气环境主要来源于自然源的影响, 但夏季风期间人为污染排放已经不可忽视, 这也得到HYSPLIT后向轨迹模式的计算验证.  相似文献   

13.
Study of precipitation chemistry over an industrial city   总被引：2，自引：2，他引：0  
The growing trend of industrialization has marked impact on the atmospheric chemistry around the globe. Such impacts are also predicted for developing countries like India. Acid precipitation due to secondary pollutants is one of them. The present investigation was conducted with an aim of studying the precipitation chemistry over Asansol city, India during the monsoon season. The rain water samples, collected on event basis during the period of June to September 2006, were analyzed for HCO3 ?, Cl?, SO4 2?, NO3 ?, NH4 +, K+, Na+, Mg2+, Ca2+ and pH using standard procedures. The study revealed that the precipitation was alkaline in nature with mean pH value of 6.08. Dominant anion in rain water samples was HCO3 ? (36 %), whereas Ca2+ was highest among the cations (53 %). The observed acidic events, based on pH value, were only 17 %, indicating the alkaline components effectively neutralize rain water over the area. This was also supported by the total alkaline to acid ion ration of 1.05. The ratio of (NO3-?+Cl?) and SO4 2? was >1, indicating that acidic properties were influenced by HNO3 and HCl. In the ratio between (Ca2++NH4 +) and (NO3 ?+SO4 2?), values >1 were obtained, indicating significant alkaline influence, which effectively prevented acid depositions in the area.  相似文献   

14.
The Vea catchment, mainly underlain by crystalline basement rocks, is located in Northern Ghana. Hydrogeochemical studies were carried out in this area with the objective of identifying the geochemical processes influencing water quality and suitability of surface and groundwater for agricultural and domestic uses. Sixty-one groundwater and four surface water samples were collected from boreholes, dams and rivers and analysed for Ca2+, Mg2+, Na+, K+, HCO3 ?, Cl?, and SO4 2?, Fetot, PO4 3?, Mntot, NH4 +, NO3 ?, NO2 ?. In addition, pH, total dissolved solids, electrical conductivity, total hardness, turbidity, colour, salinity and dissolved oxygen were analysed. Chloro-alkaline indices 1 and 2, and characterization of weathering processes suggest that the chemistry of groundwater is dominated by the interaction between water and rocks. Cation exchange and silicate weathering are the dominant processes controlling the chemical composition of the groundwater in the area studied. Mineral saturation indices indicate the presence of at least three groups of groundwater in the Vea catchment with respect to residence time. The meteoric genesis index suggests that 86% of the water samples belong to the shallow meteoric water percolation type. The findings further suggest that the groundwater and surface water in the basin studied are mainly Ca–Mg–HCO3 water type, regardless of the geology. Compared to the water quality guidelines of WHO, the study results on sodium absorption ratio, sodium percentage, magnesium hazard, permeability index and residual sodium carbonate indicate that groundwater and surface water in the Vea catchment are generally suitable for drinking and irrigation purposes.  相似文献   

15.
《Applied Geochemistry》1995,10(2):207-214
The importance of adsorption on peat for decreasing NH4+ was estimated in four overland flow areas (OFA) in northern Finland, where peat mining water is purified by conducting it across a natural mire of a given size. The effective cation exchange capacity (ECEC) values of peat in the OFAs ranged from 21.4 to 92.7 meq per 100g, being generally highest in the surface 0–15 cm. It was estimated that about 4.6–5.8% of the peat cation exchan e sites could be occupied by NH4+, corresponding to a NH4+ retention capacity of about 0.18 to 0.77 g kg−1 dry peat. Assuming that the retention was attributable to the 0–15 cm surface peat layer alone, the calculated NH4+ retention potential of OFA peat should have lasted under 6 months with the loadings imposed on the OFAs and the decreases in NH4+ amounts in peat mining water considered here. The actual duration of peat capacity to retain NH4+ in the OFAs has, however, already been shown in this research to be longer, and apparently will be so also in future, probably as a result of two processes: nitrification and subsequent N loss through denitrification, and biological assimilation. Hence, cation exchange capacity of OFA was an important property that contributed to surface water protection against eutrophication by N.  相似文献   

16.
Ammonia is a major environmental factor influencing biomethanation in full-scale anaerobic digesters. In this study, the effect of different ammonia levels on methanogenic pathways and methanogenic community composition of full-scale biogas plants was investigated. Eight full-scale digesters operating under different ammonia levels were sampled, and the residual biogas production was followed in fed-batch reactors. Acetate, labelled in the methyl group, was used to determine the methanogenic pathway by following the 14CH4 and 14CO2 production. Fluorescence in situ hybridisation was used to determine the methanogenic communities’ composition. Results obtained clearly demonstrated that syntrophic acetate oxidation coupled with hydrogenotrophic methanogenesis was the dominant pathway in all digesters with high ammonia levels (2.8–4.57 g NH4 +-N L?1), while acetoclastic methanogenic pathway dominated at low ammonia (<1.21 g NH4 +-N L?1). Thermophilic Methanomicrobiales spp. and mesophilic Methanobacteriales spp. were the most abundant methanogens at free ammonia concentrations above 0.44 g NH3-N L?1 and total ammonia concentrations above 2.8 g NH4 +-N L?1, respectively. Meanwhile, in anaerobic digesters with low ammonia (<1.21 g NH4 +-N L?1) and free ammonia (<0.07 g NH3-N L?1) levels, mesophilic and thermophilic Methanosaetaceae spp. were the most abundant methanogens.  相似文献   

17.
The concentrations and isotopic compositions of the various forms of nitrogen in silty clay sediments from the Bay of Quinte (Lake Ontario) have been determined. The total organic-N content is high throughout the sediment profiles and generally decreases with depth. On the contrary, exchangeable NH+4-N concentration is quite low and tends to increase with depth in two out of three sediment cores examined. The concentration of non-exchangeable NH+4-N and the 6 N HCl hydrolyzable NH+4-N are relatively constant with depth. Among the N fractions analyzed, the exchangeable NH+4-is most enriched in 15N. In most cases, the δ 15 N values of the N fractions remain relatively constant with sediment depth. There is no apparent correlation of δ 15 N values with the N concentration for any of the individual N fractions. The observed ranges in the δ 15 N values are: exchangeable NH+4, + 5–+10‰; 6 N HCl hydrolyzable total N and 6 N HCl hydrolyzable NH+4-N, + 3.5–+5.5‰.  相似文献   

18.
Powdered samples of some jarosite-type compounds were analysed at room temperature by 57Fe Mössbauer spectroscopy. This group of compounds is described by the formula: MFe3(SO4)2(OH)6, where M can be H3O+, Na+, K+, Rb+, Ag+, NH 4 + , Tl+, 1/2Pb2+ or 1/2Hg2+. Although all the spectra were very similar, a linear relationship between the quadrupole splitting and the iron content of the samples was observed for the monovalent jarosite-type compounds.  相似文献   

19.
The physicochemical properties and major ion chemistry of the groundwater sources from alluvial aquifers along the stretch (60 km) of Jhelum River in Kashmir Himalaya were determined in order to identify hydro-geochemical processes and their suitability for drinking purposes. The data depicted that calcium and bicarbonates were dominating among the cations and anions. The results indicate the trend of cation dominance as Ca2+ > Na+ > Mg2+ > K+, whereas anion dominance was in the order of HCO3 ? > Cl? > SO4 2?. Ratio of calcium to magnesium indicated the dissolution of Ca2+ from CaCO3, which results in an increased levels of Ca2+ in the groundwater. Interpretation of Piper Trilinear plot understands the various geochemical processes affecting the groundwater quality and shows groundwater was dominated by Ca–HCO3 type. The pH was recorded in the slightly alkalinity range 7.2–7.8 and was showing positive correlation with HCO3 ?. The chloro-alkaline indices revealed 86% of the sources exchange by a type of base-exchange reactions, rest by cation–anion exchange. Gibbs diagram revealed groundwater sources fall in the category of rock dominance. The concentration of the nitrogen compounds was in the progression of NO3–N > NH4–N > NO2–N, and the PO4 ? fluctuated from 0.12 to 0.22 mg/L. Moreover, corrosivity ratio indicated that water from the majority of sources (71%) is safe to supply using pipes without any corrosive effects, while 29% of sources are corrosive in nature and need non-corrosive pipes for transporting and lifting of groundwater. The results revealed, groundwater samples were within permissible limits as prescribed by International and National standards, for drinking purposes. The State government and NGO’s can show their interest in utilizing such water resources to overcome the shortage of drinking water in a sustainable way for the daily consumption of the people living in the vicinity of Jhelum River.  相似文献   

20.
Bone char has been used as a low-cost adsorbent for the removal of As(V) from waste water. The batch experiments show that the Langmuir isotherm describes well the adsorption behavior. The adsorption process follows a pseudo-second-order kinetic model. The column experiments were conducted at pH = 4 and 10 mg/L an initial concentration of As(V). The breakthrough curves were investigated for various conditions, such as different flow rates, column bed heights, adsorption cycles, coexisting cations and anions such as Mn2+, Al3+, PO4 3?, SO4 2? and SiO3 2?. The convection–diffusion equation was used to model the experimental transport data of As(V) for these conditions. It has been found that the coexisting cations can enhance As(V) immobilization and increase retardation factor (R f), and coexisting anions significantly decrease the diffusion coefficient (D L) of As(V). The secondary adsorption phenomena were observed in the breakthrough curves of column studies of As(V) with cations, especially Mn2+. The regeneration experiments using distilled water and 0.1 mol/L NaOH solution were done to evaluate the desorption degree. The total desorbed amounts from whole column for three experiments decreased from 8.98 to 7.67 mg and the desorption degrees increased from 0.51 to 0.71 unexpectedly, which indicates that the regeneration operation is feasible. Finally, the chemical analysis of column effluents and infrared spectroscopic analysis of absorbent both revealed that the ligand exchange and electrostatic interaction are the main removal mechanisms.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号