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 78 毫秒
1.
Barium ion cross-linked alginate beads have shown great affinity to toxic hexavalent chromium ions in aqueous solution, in contrast to the traditionally used calcium alginate beads. Our adsorption experiments were carried out by the batch contact method. The optimal pH for removal was found to be pH 4. The equilibrium was established in 4 h, and the removal efficiency of chromium(VI) was found to be 95 %. The adsorption data were applied to Langmuir, Freundlich, Dubinin–Redushkevich (D–R), and Temkin isotherm equations. Both Langmuir and Freundlich isotherm constants indicated a favorable adsorption. The value of mean sorption energy calculated from D–R isoterm indicates that the adsorption is essentially physical. The high maximum chromium(VI) adsorption capacity was determined from the Langmuir isotherm as 36.5 mg/g dry alginate beads. The chromium(VI) adsorption data were analyzed using several kinetic models such as the pseudo-first-order, pseudo-second-order, intraparticle diffusion, and Elovich models, and the rate constants were quantified. Our study suggests that barium alginate beads can be used as cost-effective and efficient adsorbents for the removal of chromium(VI) from contaminated waters.  相似文献   

2.
Asexual spores of the filamentous fungus Rhizopus arrhizus were used as the resting biomass as they tolerate chitosan gelling for mycelia growing in chitosan beads. Biosorption of lead using the dead detergent pre-treated chitosan-immobilised and grown fungal beads was performed with initial lead (II) nitrate concentrations ranging from 9.02 to 281.65 mg/L. The adsorption data were best correlated with equilibrium adsorption isotherms in the order Redlich–Peterson, Langmuir, Freundlich and Fritz–Schlünder by non-linear regression. The biosorption kinetic model of pseudo second-order (R 2 > 0.99) fitted better than pseudo first-order and modified pseudo first-order models. Among the four pseudo second-order kinetic models, the Blanchard model was the best fit for the experimental biosorption data. The rate-limiting step of biosorption of lead was shown to be intraparticle diffusion controlled according to Weber and Morris model fitting. The beads could be regenerated using 1 M nitric acid solution. This illustrated the good performance of the beads for regenerated sorption/desorption at least five cycles.  相似文献   

3.
  相似文献   

4.
In this study, sepiolite-nano zero valent iron composite was synthesized and applied for its potential adsorption to remove phosphates from aqueous solution. This composite was characterized by different techniques. For optimization of independent parameters (pH = 3–9; initial phosphate concentration = 5–100 mg/L; adsorbent dosage = 0.2–1 g/L; and contact time = 5–100 min), response surface methodology based on central composite design was used. Adsorption isotherms and kinetic models were done under optimum conditions. The results indicated that maximum adsorption efficiency of 99.43 and 92% for synthetic solution and real surface water sample, respectively, were achieved at optimum conditions of pH 4.5, initial phosphate concentration of 25 mg/L, adsorbent dosage of 0.8 g/L, and 46.26 min contact time. The interaction between adsorbent and adsorbate is better described with the Freundlich isotherm (R 2 = 0.9537), and the kinetic of adsorption process followed pseudo-second-order model. Electrostatic interaction was the major mechanisms of the removal of phosphates from aqueous solution. The findings of this study showed that there is an effective adsorbent for removal of phosphates from aqueous solutions.  相似文献   

5.
Incidence of high fluoride (F?) in groundwater (>1.5 mg/L) in two tribal belts of eastern India, one around Chukru in the Palamau district of Jharkhand and the other around Karlakot in the Nuapada district of Odisha, has been studied. The maximum concentration of F? in groundwater from dug wells and tube wells is 10.30 mg/L in Chukru and 4.62 mg/L in Karlakot. The groundwaters are mildly alkaline with pH ranges of 7.52–8.22 and 7.33–8.20 in Chukru and Karlakot, respectively. The F? concentration is positively correlated with pH, electrical conductivity and SO4 2? in both areas. The high F? in groundwater resulted mainly from dissolution of biotite and fluorapatite in quartzofeldspathic gneiss. The ionic dominance pattern (in meq/L) is mostly in the order Ca2+ > Na+ > Mg2+ > K+ among cations and HCO3 ? > SO4 2? > < Cl? > F? among anions in the Karlakot groundwater. Preliminary adsorption experiments were conducted on natural haematite iron ore and synthetic magnetite to evaluate their potential for F? removal from water. Effects of different parameters such as contact time, pH, adsorbent dose and initial F? concentration on the adsorption capacity of these materials were investigated. Strong dependence of F? removal on pH was observed for both the adsorbents. With natural haematite iron ore, the maximum F? removal of 66 % occurred at an initial pH of 3.2 for a solution with F? concentration of 3 mg/L, adsorbent dose of 7 g/L and overnight contact time. The haematite iron ore was observed to increase the pH of the F? solution. Adsorption equilibrium was not achieved with this adsorbent even after a contact time of 45.2 h. In the case of synthetic magnetite, 84 % F? removal was achieved after 2 min of contact time for a solution with F? concentration of 6 mg/L, adsorbent dose of 10 g/L and initial pH of 7. The results indicate high potential of both natural haematite iron ore and synthetic magnetite as adsorbents of F? in water.  相似文献   

6.
In present study a turbocharged, medium duty compression ignition engine was alternatively fuelled with biodiesel to investigate the changes in particulate matter composition, relative to that taken with diesel fuel. The engine was operated on an AC electrical dynamometer in accordance with an 8-mode, steady-state cycle. The numbers of particles were estimated through electrical low pressure impactor, while sulfates and trace metals were analyzed by ion chromatography and inductively coupled plasma-atomic emission spectroscopy, respectively. Nitric oxides and nitrogen dioxides were measured separately using SEMTECH-DS. Experimental results revealed that, on account of elevated ratios of nitrogen dioxide to nitrogen oxides, mean accumulation mode particles were 42 % lower with biodiesel. On the other hand, nuclei mode particles were higher with biodiesel, owing to heterogeneous nucleation and accounting for an increase in sulfate emissions up to 8 % with biodiesel as compared to diesel. On the average, trace metal emissions were significantly reduced showing 65–85.4 % reduction rates with biodiesel, relative to its counterpart. Further to this, individual congeners such as iron, calcium, and sodium were the predominant elements of the trace metals emitted from engine. The mean relative decrease in iron and calcium was 89–97.8 and 77.6–87 %, respectively, while the relative rise in sodium was in the range of 29–46 % with biodiesel. Further, elements such as zinc, chromium, and aluminum showed substantial abatement, whereas potassium, magnesium, and manganese exhibited irregular trends on account of variable engine loads and speeds during the various modes of cycle.  相似文献   

7.
The present study attempted to identify the efficient hazardous metal-removing sorbent from specific types of soil, upper and middle layer shirasu, shell fossil, tuff, akadama and kanuma soils of Japan by physico-chemical and metal (arsenic, cadmium and lead) removal characterizations. The physico-chemical characteristics of soil were evaluated using X-ray diffraction and scanning electron microscopy with energy dispersive spectroscopy techniques, whereas metal removal properties of soil were characterized by analyzing removal capacity and sorption kinetics of potential metal-removing soils. The chemical characteristics revealed that all soils are prevalently constituted of silicon dioxide (21.83–78.58 %), aluminum oxide (4.13–38 %) and ferrous oxide (0.835–7.7 %), whereas calcium oxide showed the highest percentage (65.36 %) followed by silicon dioxide (21.83 %) in tuff soil. The results demonstrated that arsenic removal efficiency was higher in elevated aluminum oxide-containing akadama (0.00452 mg/L/g/h) and kanuma (0.00225 mg/L/g/h) soils, whereas cadmium (0.00634 mg/L/g/h) and lead (0.00693 mg/L/g/h) removal efficiencies were maximum in elevated calcium oxide-containing tuff soil. Physico-chemical sorption and ion exchange processes are the metal removal mechanisms. The critical appraisal of three metal removal data also clearly revealed cadmium > lead > arsenic order of removal efficiency in different soils, except in tuff and akadama soils followed by lead > cadmium > arsenic. It clearly signified that each type of soil had a specific metal adsorption affinity which was regulated by the specific chemical composition. It may be concluded that akadama would be potential arsenic-removing and tuff would be efficient cadmium and lead-removing soil sorbents.  相似文献   

8.
地下水中钙和镁的离子色谱法同时测定   总被引：2，自引：0，他引：2  
改进了离子色谱分析地下水中钙和镁的方法。以IonPac CS12A为分离柱,稀盐酸为淋洗液,电导检测器检测,对地下水中的锂、钾、钠、钙和镁进行同时测定。方法具有较宽的线性范围和较高的灵敏度,钙、镁的浓度分别在0～500mg/L和0～250mg/L内呈良好的线性关系;钙的检出限为1.50μg/L,镁的检出限为0.89μg/L。对不同浓度钙、镁水质标准样品进行分析测定,同时对实际样品进行不同稀释倍数分析验证,方法精密度(RSD,n=8)为0.19%～1.89%,无显著的基体效应影响。方法可满足全国地下水调查评价规范要求,适于地下水样品中锂、钾、钠、钙和镁离子的同时测定。  相似文献   

9.
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   

10.
This study aims to attempt a treatment strategy based on fungi immobilized on silica-alginate (biocomposites) for removal of phenolic compounds in olive oil mill wastewater (OMW), OMW supplemented (OMWS) with phenolic compounds and water supplemented (WS) with phenolic compounds, thus decreasing its potential impact in the receiving waters. Active (alive) or inactive (death by sterilization) Pleurotus sajor caju was encapsulated in alginate beads. Five beads containing active and inactive fungus were placed in a mold and filled with silica hydrogel (biocomposites). The biocomposites were added to batch reactors containing the OMW, OMWS and WS. The treatment of OMW, OMWS and WS by active and inactive biocomposites was performed throughout 28 days at 25 °C. The efficiency of treatment was evaluated by measuring the removal of targeted organic compounds, chemical oxygen demand (COD) and relative absorbance ratio along the time. Active P. sajor caju biocomposites were able to remove 64.6–88.4 % of phenolic compounds from OMW and OMWS and 91.8–97.5 % in water. Furthermore, in the case of OMW there was also a removal of 30.0–38.1 % of fatty acids, 68.7 % of the sterol and 35 % of COD. The silica–alginate–fungi biocomposites showed a high removal of phenolic compounds from OMW and water. Furthermore, in the application of biocomposites to the treatment of OMW it was observed also a decrease on the concentration of fatty acids and sterols as well as a reduction on the COD.  相似文献   

11.
The Cuatrociénegas area is useful for the investigation of the effect of groundwater extraction in the Chihuahuan freshwater xeric ecoregion. It has been investigated at this time using a selection of geochemical indicators (major, minor and trace elements) and δ34S data, to characterize the origin of groundwater, the main geochemical processes and the mineral/groundwater interactions controlling the baseline geochemistry. The area is composed of limestones of Mesozoic age, with a composite thickness of about 500 m, overlaid by basin fill (poorly consolidated young sediments). Substantial water extraction and modification of natural discharges from the area along the last century have produced a detrimental impact on ecosystem structure and function. Water–rock interactions, mixing and evaporative processes dominate the baseline groundwater quality. Natural recharge is HCO3–Ca type in equilibrium with calcite, low salinity (TDS?<?500 mg/L), Cl? lower than 11 mg/L and average Li+ concentration of 0.005 mg/L. Along the groundwater flow systems, δ34S evidence and mass transfer calculations indicate that Cretaceous gypsum dissolution and dedolomitization reactions adjust water composition to the SO4–Ca type. The increase of water–rock interaction is reflected by Cl? values increase (average 68 mg/L), TDS up to about 1500 mg/L and an average Li+ concentration of 0.063 mg/L. Calculations with chemical geothermometers indicate that temperature at depth could be at maximum of 15–20 °C higher than field-measured temperature for pozas. After groundwater is discharged to the surface, chemical evolution continues; water evaporation, CO2 degassing and precipitation of minerals such as gypsum, calcite and kaolinite represent the final processes and reactions controlling water chemical composition.  相似文献   

12.
Nanoscale zero-valent iron flakes for groundwater treatment   总被引：1，自引：0，他引：1  
Even today the remediation of organic contaminant source zones poses significant technical and economic challenges. Nanoscale zero-valent iron (NZVI) injections have proved to be a promising approach especially for source zone treatment. We present the development and the characterization of a new kind of NZVI with several advantages on the basis of laboratory experiments, model simulations and a field test. The developed NZVI particles are manufactured by milling, consist of 85 % Fe(0) and exhibit a flake-like shape with a thickness of <100 nm. The mass normalized perchloroethylene (PCE) dechlorination rate constant was 4.1 × 10?3 L/g h compared to 4.0 × 10?4 L/g h for a commercially available reference product. A transport distance of at least 190 cm in quartz sand with a grain size of 0.2–0.8 mm and Fe(0) concentrations between 6 and 160 g/kg (sand) were achieved without significant indications of clogging. The particles showed only a low acute toxicity and had no longterm inhibitory effects on dechlorinating microorganisms. During a field test 280 kg of the iron flakes was injected to a depth of 10–12 m into quaternary sand layers with hydraulic conductivities ranging between 10?4 and 10?5 m/s. Fe(0) concentrations of 1 g/kg (sand) or more [up to 100 g/kg (sand)] were achieved in 80 % of the targeted area. The iron flakes have so far remained reactive for more than 1 year and caused a PCE concentration decrease from 20.000–30.000 to 100–200 µg/L. Integration of particle transport processes into the OpenGeoSys model code proved suitable for site-specific 3D prediction and optimization of iron flake injections.  相似文献   

13.
This study was conducted to evaluate the efficiency of low-cost adsorbents including bentonite, kaolinite and zeolite saturated with calcium and potassium, potato and wheat residues, and three metal oxide nanoparticles functionalized with an acidic extract of potato residues in improving the quality of sodic waters. The optimization of factors such as pH, contact time, and adsorbent dosage was investigated using a solution containing sodium, calcium, magnesium, and potassium. The optimal pH and contact time were 7.0 and 24 h, respectively. The optimal dosage for using functionalized nanoparticles was 0.1 g and for using other adsorbents was 1.0 g. The sodium exchange isotherms were conducted in binary sodium–calcium and sodium–potassium and quaternary sodium–calcium–magnesium–potassium systems. Zeolite saturated with potassium was the most effective adsorbent in removing sodium from aqueous solutions with an average removal efficiency of 69.2 and 66.5 % in binary and quaternary systems, respectively. Freundlich and Langmuir equations fitted well to experimental data in both binary and quaternary systems. Cation selectivity coefficients calculated based on the Gaines–Thomas convention varied with changing pH and adsorbent dosage. Graphical and statistical evaluations confirmed that the mechanistic cation exchange model using average Gaines–Thomas selectivity coefficients in geochemical PHREEQC program was able to successfully simulate the sodium exchange on different adsorbents in both systems. The Gaines–Thomas selectivity coefficient values greater than unity and as a consequence, the negative values of the Gibbs free energy change of adsorption indicated that sodium exchange reactions in the presence of different adsorbents used is this study were exergonic and spontaneous.  相似文献   

14.
We present high-precision iron and magnesium isotopic data for diverse mantle pyroxenite xenoliths collected from Hannuoba, North China Craton and provide the first combined iron and magnesium isotopic study of such rocks. Compositionally, these xenoliths range from Cr-diopside pyroxenites and Al-augite pyroxenites to garnet-bearing pyroxenites and are taken as physical evidence for different episodes of melt injection. Our results show that both Cr-diopside pyroxenites and Al-augite pyroxenites of cumulate origin display narrow ranges in iron and magnesium isotopic compositions (δ57Fe = ?0.01 to 0.09 with an average of 0.03 ± 0.08 (2SD, n = 6); δ26Mg = ? 0.28 to ?0.25 with an average of ?0.26 ± 0.03 (2SD, n = 3), respectively). These values are identical to those in the normal upper mantle and show equilibrium inter-mineral iron and magnesium isotope fractionation between coexisting mantle minerals. In contrast, the garnet-bearing pyroxenites, which are products of reactions between peridotites and silicate melts from an ancient subducted oceanic slab, exhibit larger iron isotopic variations, with δ57Fe ranging from 0.12 to 0.30. The δ57Fe values of minerals in these garnet-bearing pyroxenites also vary widely (?0.25 to 0.08 in olivines, ?0.04 to 0.25 in orthopyroxenes, ?0.07 to 0.31 in clinopyroxenes, 0.07 to 0.48 in spinels and 0.31–0.42 in garnets). In addition, the garnet-bearing pyroxenite shows light δ26Mg (?0.43) relative to the mantle. The δ26Mg of minerals in the garnet-bearing pyroxenite range from ?0.35 for olivine and orthopyroxene, to ?0.34 for clinopyroxene, 0.04 for spinel and ?0.68 for garnet. These measured values stand in marked contrast to calculated equilibrium iron and magnesium isotope fractionation between coexisting mantle minerals at mantle temperatures derived from theory, indicating disequilibrium isotope fractionation. Notably, one phlogopite clinopyroxenite with an apparent later metasomatic overprint has the heaviest δ57Fe (as high as 1.00) but the lightest δ26Mg (as low as ?1.50) values of all investigated samples. Overall, there appears to be a negative co-variation between δ57Fe and δ26Mg in the Hannuoba garnet-bearing pyroxenite and in the phlogopite clinopyroxenite xenoliths and minerals therein. These features may reflect kinetic isotopic fractionation due to iron and magnesium inter-diffusion during melt–rock interaction. Such processes play an important role in producing inter-mineral iron and magnesium isotopic disequilibrium and local iron and magnesium isotopic heterogeneity in the subcontinental mantle.  相似文献   

15.
Health hazards from heavy metal pollution in water systems are a global environmental problem. Of similar concern is sludge that results from wastewater treatment due to unsatisfactory sludge management technology. Therefore, the effectiveness of using Mg–Al-layered double hydroxide in the removal of heavy metals from mine wastewater was tested and compared with that of calcium hydroxide [Ca(OH)2], which is a common treatment method for heavy metal removal. Initially, the mine wastewater contained cations of the heavy metals iron (Fe), zinc (Zn), copper (Cu), and lead (Pb). The Mg–Al-layered double hydroxides were able to remove 371, 7.2, 121, and 0.4 mg/L of these pollutants, respectively, using the co-precipitation method. The removal of these metals is most effective using 0.5 g Mg–Al-layered double hydroxide (Mg/Al molar ratio 4) and 20 min of shaking. Zn was removed by the formation of Zn(NO3)(OH)·H2O and Zn5(NO3)2(OH)8 when LDH, Mg/Al molar ratios of 4 and 2, respectively, were used. Similarly, Fe, Cu, and Pb were removed by the formation of Fe–Al-layered double hydroxide, Cu2(OH)3·NO3 and Pb4(OH)4(NO3)4, respectively. While Ca(OH)2 is also capable of reducing the heavy metal concentrations below the Japanese recommended values, this analysis shows that using 0.5 g Mg–Al-layered double hydroxide is a better treatment condition for mine wastewater, because it generates lower sludge volumes than 0.1 g of Ca(OH)2. The measured sludge volume was 1.5 mL for Mg–Al-layered double hydroxide and 2.5 mL for Ca(OH)2, a nearly twofold further reduction.  相似文献   

16.
Regional study on the impact of variations in input rainfall over groundwater quality and its suitability for utilitarian purposes is essential for its extraction and management. Water chemistry from 456 observations wells for 2007–2011 period in hard rock Basaltic terrain of Upper Godavari basin is supported with 8 field samples (in 2014) in this analysis. Based on mean annual rainfall (MAR), four narrow climatic zones are identified in the basin, defined as “humid” (MAR > 1600 mm), “sub-humid” (1600–1000 mm), “semi-arid” (1000–600 mm), and “arid” (MAR < 600 mm). NICB ratio (<±10%), and anionic percentages demarcated the polluted areas from rest “good data”, composing of 1818 samples. Hydrochemical facies are studied using Piper diagram, secondary alkalinity exceeded 50% and not one cation–anion pair exceeded 50%, and silicate–carbonate plot, arid zone nearer to silicate pole indicated the dominance of SiO2 in Ca/Na vs Mg/Na plot. These geochemical variations emphasize a detailed study on role of climatic gradient on groundwater suitability for different purposes, for groundwater extraction, and its management. Suitability of groundwater for drinking based on water quality indices (WQI) indicated 98% of the samples as suitable (WQI < 50%). TDS in humid zone is 150–500 and 500–1000 mg/L in rest of the zones with ～68% in permissible range, 15% as hard water (TDS > 600 mg/L) and not acceptable for drinking. Suitability of groundwater for irrigation is studied using sodium percentage (Na %), Wilcox diagram, sodium absorption ratio (SAR), US salinity diagram, residual sodium carbonate (RSC), permeability index (PI), Kelly’s ratio (KR), ancd magnesium absorption ratio (MgAR). Na % in four zones is < 60% and permissible for irrigation. Very few water samples fall in “doubtful to unsuitable” and “unsuitable” category of Wilcox diagram. Region is observed to have SAR < 6, indicating that water would not cause any problem to the soil and crop. Humid and sub-humid zones belonged to C1S1 and C2S1 categories (low and medium sodium), while semi-arid extended to C3S1 category (salinity hazard zone) in US salinity plot. RSC for all the three zones ranged from 1 to 1.5 meq/L, with 90–95% of the area safe for irrigation. Out of 1818 samples, 1129 belonged to class 2 of PI classification (PI ranging from 25 to 75%) while rest 689 samples had PI >75% (class 1). KR varied from 0.05 to 12.81, with 70–80% of the area having KR < 1. MgAR ratio ranged from 67% to 96%, with sub-humid, humid zones having higher Mg concentrations (increased salinity). Thus, 90% of the samples indicated non-alkaline water with 1% of normal alkalinity. Hence, the current study systematically analyzed the effect of precipitation and geology on groundwater quality and on its usability for various purposes. This stepwise procedure categorized the regions, and the same can be adopted for any regional hydrogeochemical studies.  相似文献   

17.
There is an urgent need for characterization of leachate arising from waste disposal to ensure a corresponding effective leachate management policy. Field and laboratory studies have been carried out to investigate the impact of municipal landfill leachate on the underlying groundwater at a site in West Malaysia. The solid waste was disposed of directly onto an unprotected natural soil formation. This situation was made worse by the shallow water table. The hydrochemical composition of groundwater in the vicinity of the site (background) is a dilute mixed cation, bicarbonate water. The high ionic balance error of ~13.5% reveals that the groundwater body underneath the site was a highly contaminated leachate rather than contaminated groundwater. Elevated concentration of chloride (355.48 mg/L), nitrate (10.40 mg/L as NO3), nitrite (14.59 mg/L), ammoniacal-N (11.61 mg/L), sodium (227.56 mg/L), iron (0.97 mg/L), and lead (0.32 mg/L) measured downgradient indicate that the contamination plume has migrated further away from the site. In most cases, the concentration of these contamination indicators, together with the ranges of sodium percentage (66.3–89.9%) and sodium adsorption ratio (10.1–19.7%), were found to be considerably higher than the limit values of safe water for both domestic and irrigation purposes, respectively.  相似文献   

18.
Sewage treatment station in oilfield needs a new process to meet the desired requirements. A new process was proposed to meet the discharge standards, which consisted of the following sub-processes: electrochemical treatment → coagulation treatment → integrated biochemical treatment of moving bed biofilm reactor and membrane bio-reactor → combined treatment process of macroporous adsorption resin. Electrochemical treatment included 5 electrolytic cells, total volume of which was 10 L. The PFS was chosen as the coagulants in the coagulation treatment, and the removal rate of COD could reach 66% when the dosage of PFS was 500 mg/L. The biochemical treatment consisted of anoxic tank, aerobic tank and membrane zone, and the removal rate of COD was about 55–70% when HRT was 12 h. SD300 resin was chosen as the best adsorbent in the treatment using macroporous adsorption resin. In addition, the effluent COD after coagulation treatment process becomes about 180 mg/L, the effluent COD after biological treatment becomes about 50 mg/L, and the last effluent COD with the macroporous adsorption resin becomes about 20 mg/L. The three-dimensional fluorescence spectrum was used to analyze the differences in types of organic matters in water samples between the raw water and the treated one. The results demonstrated that the new process meets the needs of wastewater treatment.  相似文献   

19.
Investigations were undertaken into the quality of surface water and groundwater bodies within the Upper Tigris Basin in Turkey to determine their suitability for potable and agricultural use. In the study area, the majority of the groundwater and surface water samples belong to the calcium–magnesium–bicarbonate type (Ca–Mg–HCO3) or magnesium–calcium–bicarbonate type (Mg–Ca–HCO3). Chemical analysis of all water samples shows that the mean cation concentrations (in mg/L) were in the order Ca2+ > Mg2+ > Na+ > K+ and that of anions are in the order \( \text{HCO}_{3}^{ - } \) > \( \text{SO}_{4}^{2 - } \) > Cl? > \( \text{CO}_{3}^{ - } \) for all groundwater and surface water samples. The Mg2+/Ca2+ ratio ranges from 0.21 to 1.30 with most of the values greater than 0.5, indicating that weathering of dolomites is dominant in groundwater. The analysis reveals that all of the samples are neutral to slightly alkaline (pH 7.0–8.7). Groundwater and surface water suitability for drinking usage was evaluated according to the World Health Organization and Turkish Standards (TSE-266) and suggests that most of the samples are suitable for drinking. Various determinants such as sodium absorption ratio, percent sodium (Na %), residual sodium carbonate and soluble sodium percentage revealed that most of the samples are suitable for irrigation. According to MH values, all of the well water samples were suitable for irrigation purposes, but 80 and 81.82% of Zillek springs and surface water samples were unsuitable. As per the PI values, the water samples from the study area are classified as Class I and Class II and are considered to be suitable for irrigation.  相似文献   

20.
The present study was carried out in Singrauli area of the north India to know the water quality at selected sites. Physico-chemical parameters like pH, total dissolved solids (TDS), bicarbonate, hardness, calcium, magnesium, sodium, potassium, chloride, sulfate, copper, iron, cobalt, manganese, zinc, and chromium were analyzed in 27 water samples. Locations selected for sampling were based on the preliminary field survey carried out to understand the overall impact of mining and industrialization on the surface and groundwater resources of Singrauli. Base map, drainage map, and land use/land cover of the study area were prepared from Survey of India topographic map 63 L/12 on 1:50000 scale and satellite data of IRS P6 LISS III 4th May 2010. Land use were categorized into 15 categories out of which major area occupied by open forest covers 20.33 %, uncultivated land 20.25 %, cultivated land 12.60 %, dense forest 11.00 %, and other categories cover 35.82 %. The results obtained are compared with World Health Organisation standards for drinking water quality. The physico chemical analysis shows alkaline nature of water, soft to moderately soft, TDS and total alkalinity exceeds the desirable limit. The major ions in water like calcium, and magnesium are within desirable limits, and sulfate and potassium exceed in limit at some locations, whereas sodium and chloride show higher values. The minor ions like copper and zinc show values within desirable limits whereas iron, cobalt, and chromium show higher values than the desirable limits which deteriorate the quality of water.  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