Removal of Acid Red 18 dye from Aqueous Solutions Using Nanoscale Zero-Valent Iron

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Ahmad Reza Yari

2015-08-01

Full Text Available Background and Purpose:Organic dyes with a complex structure are often toxic, carcinogenic, mutagenic, non-biodegradation and stable in the environment and if released to the environment without treatment can endanger the environment and human health. The aim was to evaluate the performance nanoscalezero-valent iron (NZVI in the removal of dye acid red 18 (AR18 from aqueous solutions. Materials and Methods:This study was conducted at the laboratory scale. In this study, the removal efficiency of AR18 from a synthetic solution by NZVI was investigated. As well as the effect of solution pH, dye concentration, the concentration of NZVI and contact time in decolorization efficiency was investigated. Results:The results show that in pH = 3, contact time of 80 minutes, dye concentration of 25 mg/l and concentration of NZVI of 2 g/l, the removal efficiency was about 94%. Conclusion:According to the results of experiments, NZVI has high efficiency in removal of AR18 from aqueous solution.

The influence of small-scale interlayer heterogeneity on DDT removal efficiency for flushing technology

Science.gov (United States)

Wang, Xingwei; Chen, Jiajun

2017-06-01

With an aim to investigate the influence of small-scale interlayer heterogeneity on DDT removal efficiency, batch test including surfactant-stabilized foam flushing and solution flushing were carried out. Two man-made heterogeneous patterns consisting of coarse and fine quartz sand were designed to reveal the influencing mechanism. Moreover, the removal mechanism and the corresponding contribution by foam flushing were quantitatively studied. Compared with surfactant solution flushing, the DDT removal efficiency by surfactant-stabilized foam flushing increased by 9.47% and 11.28% under heterogeneous patterns 1 and 2, respectively. The DDT removal contributions of improving sweep efficiency for heterogeneous patterns 1 and 2 by foam flushing were 40.82% and 45.98%, and the contribution of dissolving capacity were 59.18% and 54.02%, respectively. The dissolving capacity of DDT played a major role in DDT removal efficiency by foam flushing under laboratory conditions. And the DDT removal contribution of significant improving sweep efficiency was higher than that of removal decline caused by weak solubilizing ability of foam film compared with solution flushing. The obtained results indicated that the difference of DDT removal efficiency by foam flushing was decreased under two different heterogeneous patterns with the increase of the contribution of improving foam flushing sweep efficiency. It suggested that foam flushing can reduce the disturbance from interlayer heterogeneity in remediating DDT contaminated heterogeneous medium.

Efficiency of Electrocoagulation for Removal of Reactive Yellow 14 from Aqueous Environments

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Ahmad Reza Yaria

2013-09-01

Full Text Available Background & Aims of the Study: Discharge of textile industry colored wastewater without enough treatment into natural water resources cause serious pollution. Most of the conventional wastewater treatment methods are not effective enough to remove these dyes from wastewater. In this study, efficiency of electrocoagulation process with iron electrodes for treatment of Reactive Yellow 14 dye from synthetic solution has been studied and concluded. Materials & Methods: This experiment was conducted in a batch system with a volume of 2 L that had been equipped with 4 iron electrodes. The effect of operating parameters, such as voltage, time of reaction, initial dye concentration, and interelectrode distance on the dye removal efficiency was investigated. Results: In optimum condition (pH 2, voltage 40 V, electrolysis time 25 min, and interelectrode distance 1 cm, electrocoagulation method was able to remove 99.27% of Reactive Yellow 14 from synthetic solution. Conclusions: Electrocoagulation process by iron electrode is an efficient method for removal of reactive dyes from colored solution.

Lanthanum-modified bentonite: potential for efficient removal of phosphates from fishpond effluents.

Science.gov (United States)

Kurzbaum, Eyal; Raizner, Yasmin; Cohen, Oded; Rubinstein, Guy; Bar Shalom, Oded

2017-06-01

Adsorption has been suggested as an effective method for removing phosphates from agricultural wastewater effluents that contain relatively high phosphate concentrations. The present study focused on the use of a bentonite-lanthanum clay (Phoslock ® ) for reducing the dissolved phosphate concentration in fishpond effluents. Batch experiments with synthetic phosphate-spiked solutions and with fishpond effluents were performed in order to determine adsorption equilibrium isotherms and kinetics as well as to determine the efficiency of Phoslock ® in removing phosphate from these solutions. In the synthetic phosphate-spiked solution, the mean maximum phosphate adsorption capacity was 92 mg Phoslock ® /mg phosphate removal. A ratio of 50, 100, and 200 mg Phoslock ® /mg phosphate removal was found for complete phosphate removal from the fishpond effluents, where higher doses of Phoslock ® led to a faster removal rate (94% removal within the first 150 min). These results show that bentonite-lanthanum clay can be employed for designing a treatment process for efficient phosphate removal from fishpond effluents.

Efficient removal of uranium from aqueous solution by zero-valent iron nanoparticle and its graphene composite

International Nuclear Information System (INIS)

Li, Zi-Jie; Wang, Lin; Yuan, Li-Yong; Xiao, Cheng-Liang; Mei, Lei; Zheng, Li-Rong; Zhang, Jing; Yang, Ju-Hua; Zhao, Yu-Liang; Zhu, Zhen-Tai; Chai, Zhi-Fang; Shi, Wei-Qun

2015-01-01

Highlights: • Uranium removal by ZVI-nps: independent of pH, the presence of CO 3 2− , humic acid, or mimic groundwater constituents. • Rapid removal kinetics and sorption capacity of ZVI-nps is 8173 mg U/g. • Two reaction mechanisms: sufficient Fe 0 → reductive precipitation as U 3 O 7 ; insufficient Fe 0 → hydrolysis precipitation of U(VI). • Fe/graphene composites: improved kinetics and higher U(VI) reduction ratio. - Abstract: Zero-valent iron nanoparticle (ZVI-np) and its graphene composites were prepared and applied in the removal of uranium under anoxic conditions. It was found that solutions containing 24 ppm U(VI) could be completely cleaned up by ZVI-nps, regardless of the presence of NaHCO 3 , humic acid, mimic groundwater constituents or the change of solution pH from 5 to 9, manifesting the promising potential of this reactive material in permeable reactive barrier (PRB) to remediate uranium-contaminated groundwater. In the measurement of maximum sorption capacity, removal efficiency of uranium kept at 100% until C 0 (U) = 643 ppm, and the saturation sorption of 8173 mg U/g ZVI-nps was achieved at C 0 (U) = 714 ppm. In addition, reaction mechanisms were clarified based on the results of SEM, XRD, XANES, and chemical leaching in (NH 4 ) 2 CO 3 solution. Partially reductive precipitation of U(VI) as U 3 O 7 was prevalent when sufficient iron was available; nevertheless, hydrolysis precipitation of U(VI) on surface would be predominant as iron got insufficient, characterized by releases of Fe 2+ ions. The dissolution of Fe 0 cores was assigned to be the driving force of continuous formation of U(VI) (hydr)oxide. The incorporation of graphene supporting matrix was found to facilitate faster removal rate and higher U(VI) reduction ratio, thus benefitting the long-term immobilization of uranium in geochemical environment

Arsenic Removal Efficiency in Aqueous Solutions Using Reverse Osmosis and Zero-Valent Iron Nanoparticles

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Niloofar Saboori

2018-01-01

Full Text Available Arsenic is one of the most hazardous pollutants of water resources which threaten human health as well as animals. Therefore arsenic removal from water resources is the priority of health programs. There are several ways to remove arsenic. In this study, reverse osmosis and zero-valent iron nanoparticles methods have been used in a laboratory scale. To perform the test, the variables of temperature, arsenic concentration, pH, iron nanoparticle concentration and mixing time were considered. The results indicated that in both methods of reverse osmosis and iron nanoparticle, through increasing arsenic concentration, arsenic removal efficiency has been also increased. At concentration of 1.5 mg per litre in reverse osmosis method, the maximum efficiency was achieved by 98% and 95.2% removal of arsenic respectively. The effect of temperature and pH were similar in reverse osmosis; by increasing these two variables, arsenic removal percentage also increased. The highest removal rates of 95.98% and 95.56% were observed at pH 9 and Temperature 30oC respectively. The results indicated that in iron nanoparticles method the arsenic removal efficiency increases by increasing mixing time and temperature, while it decreases with increasing pH.

Removal of trace Cd2+ from aqueous solution by foam fractionation.

Science.gov (United States)

Lu, Jian; Li, Ying; Zhang, Sen; Sun, Yange

2015-04-09

In recent years, aqueous foam was known as an efficient technique with high potential on being used to remove heavy metal ions from the polluted water, not only because of the low cost, simple operation, but also ascribed to the high removal efficiency of trace heavy metal ions and would not cause secondary pollution to the environment. In this paper, the removal of Cd(2+) from aqueous solution by aqueous foam stabilized by a kind of novel anionic-nonionic surfactant sodium trideceth-4 carboxylate (AEC) was investigated. The effect of conditions such as surfactant/metal ions molar ratio, surfactant concentration on the removal efficiency was studied. In large concentration range of surfactant, the removal rate was higher than 90%, and could reach up to 99.8% under the optimum conditions. The Zeta potential of gas bubbles in the AEC solutions was determined to verify the combination between the negative charged group heads of surfactant molecules and heavy metal ions, and isothermal titration calorimeter (ITC) determination was utilized to demonstrate the interaction, which helped to understand the mechanisms more clearly. Copyright © 2015 Elsevier B.V. All rights reserved.

Removal of dexamethasone from aqueous solution and hospital wastewater by electrocoagulation

International Nuclear Information System (INIS)

Arsand, Daniel R.; Kümmerer, Klaus; Martins, Ayrton F.

2013-01-01

This study is concerned with the removal of the anti-inflammatory dexamethasone from aqueous solution and hospital wastewater by electrocoagulation. The variation of the toxicity during the electrocoagulation was also studied through experiments that were designed and optimized by means of response surface methodology. The coagulation efficiency was evaluated by measuring the dexamethasone concentration by high performance liquid chromatography coupled to a diode array detector. In addition, variation was evaluated through a Vibrio fischeri test. The results showed an increase in the removal of dexamethasone (up to 38.1%) with a rise of the current applied and a decrease of the inter-electrode distance, in aqueous solutions. The application to hospital effluent showed similar results for the removal of dexamethasone. The main effect of the electrocoagulation was that it removed colloids and reduced the organic load of the hospital wastewater. Regarding the current applied, the calculated energy efficiency was 100%. Without pH adjustment of the aqueous solution or hospital wastewater, the residual aluminum concentration always remained lower than 10 mg L −1 , and, with adjustment (to pH 6.5), lower than 0.30 mg L −1 , at the final stage. No toxicity variation was observed during the electrocoagulation process in aqueous solution, either in the presence or absence of dexamethasone. - Highlights: ► Removal of DEX and organic load from aqueous solution and hospital wastewater by EC ► Evaluation of the toxicity during the removal of DEX by EC ► Suggestion of the EC process as a pretreatment for subsequent processes

Removal of dexamethasone from aqueous solution and hospital wastewater by electrocoagulation

Energy Technology Data Exchange (ETDEWEB)

Arsand, Daniel R., E-mail: danielarsand@pelotas.ifsul.edu.br [Chemistry Department, Federal University of Santa Maria, RS (Brazil); Kümmerer, Klaus, E-mail: klaus.kuemmerer@leuphana.de [Institute for Environmental Chemistry, Leuphana University Lüneburg (Germany); Martins, Ayrton F., E-mail: martins@quimica.ufsm.br [Chemistry Department, Federal University of Santa Maria, RS (Brazil)

2013-01-15

This study is concerned with the removal of the anti-inflammatory dexamethasone from aqueous solution and hospital wastewater by electrocoagulation. The variation of the toxicity during the electrocoagulation was also studied through experiments that were designed and optimized by means of response surface methodology. The coagulation efficiency was evaluated by measuring the dexamethasone concentration by high performance liquid chromatography coupled to a diode array detector. In addition, variation was evaluated through a Vibrio fischeri test. The results showed an increase in the removal of dexamethasone (up to 38.1%) with a rise of the current applied and a decrease of the inter-electrode distance, in aqueous solutions. The application to hospital effluent showed similar results for the removal of dexamethasone. The main effect of the electrocoagulation was that it removed colloids and reduced the organic load of the hospital wastewater. Regarding the current applied, the calculated energy efficiency was 100%. Without pH adjustment of the aqueous solution or hospital wastewater, the residual aluminum concentration always remained lower than 10 mg L{sup −1}, and, with adjustment (to pH 6.5), lower than 0.30 mg L{sup −1}, at the final stage. No toxicity variation was observed during the electrocoagulation process in aqueous solution, either in the presence or absence of dexamethasone. - Highlights: ► Removal of DEX and organic load from aqueous solution and hospital wastewater by EC ► Evaluation of the toxicity during the removal of DEX by EC ► Suggestion of the EC process as a pretreatment for subsequent processes.

Removal of boron from aqueous solution using cryptocrystalline magnesite

CSIR Research Space (South Africa)

Masindi, Vhahangwele

2016-05-01

Full Text Available of Water Reuse and Desalination Removal of boron from aqueous solution using cryptocrystalline magnesite Vhahangwele Masindi and Mugera W. Gitari Abstract The present study aimed to evaluate the efficiency of using cryptocrystalline magnesite...

Study of iodine removal efficiency in self-priming venturi scrubber

International Nuclear Information System (INIS)

Ali, Majid; Yan, Changqi; Sun, Zhongning; Gu, Haifeng; Wang, Junlong

2013-01-01

Highlights: ► Study of iodine removal efficiency in a self-priming venturi scrubber. ► Investigation of iodine removal efficiency at different gas and liquid flow rates. ► Investigation of different inlet concentrations of iodine. ► Mathematical model based on mass transfer. - Abstract: Venturi scrubber is used in filtered vented containment system of nuclear power plants to remove the gaseous pollutants from contaminated gas during severe accidents. In this research, an experimental and theoretical investigation has been carried out to study the iodine removal efficiency in a self-priming venturi scrubber. The aqueous solution is prepared by adding weight percentage of sodium hydroxide 0.5% and sodium thiosulphate 0.2% in scrubbing water to increase the absorbance of inorganic iodine (I 2 ) from the contaminated gas during emission. The iodine removal efficiency is investigated at various gas and liquid flow rates, and iodine inlet concentrations. The iodine removal efficiency is measured experimentally by measuring the inlet and outlet concentration of iodine at sampling ports. The petite droplets are formed in a venturi scrubber to absorb the iodine through the mass transfer phenomenon. A mathematical model for mass transfer based on a gas liquid interface is employed for the verification of experimental results. The contact time between iodine and scrubbing solution depends on the total volumetric flow of gas and liquid, and volume of throat and diffuser of the venturi scrubber. Sauter mean diameter is calculated from the Nukiyama and Tanasawa correlation. Steinberger and Treybal’s correlation is used to measure the mass transfer coefficient for the gas phase. The results calculated from the model under predict the experimental data

Phosphorous removal from aqueous solution can be enhanced through the calcination of lime sludge.

Science.gov (United States)

Bal Krishna, K C; Niaz, Mohamed R; Sarker, Dipok C; Jansen, Troy

2017-09-15

Water treatment plants generate an enormous amount of the sludge which is normally treated as waste. In the recent past, many investigations have been focused on developing an economical adsorbent using water treatment sludge to remove phosphorous (P) from aqueous solutions. However, the great extents of the studies have been limited in the use of alum- and iron-based sludges. This study, therefore, investigated the P removal performance of the calcined lime sludge. Calcined lime sludge at 700 °C significantly enhanced the P removal efficiency whereas marginal improvement was noted when the sludge calcined at 400 °C was tested. With increase P removal efficiency, final pH values of the solution also significantly increased. P removal efficiency of the calcined sludge decreased with increasing the initial P concentrations. However, the removal efficiency could be improved by increasing the weight of the sludge. Further analysis demonstrated that P removal trend followed both pseudo-second order and diffusion-chemisorption kinetics signifying the P removal is potentially due to a multi-mechanistic reaction in which, the process is controlled by intra-particle diffusion followed by chemisorptions. Copyright © 2017 Elsevier Ltd. All rights reserved.

Efficiency of Advanced H2O2/ZnO Oxidation Process in Ceftriaxone Antibiotic Removal from Aqueous Solutions

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Maryam Noroozi cholcheh

2017-11-01

Full Text Available A major concern about pharmaceutical pollution is the presence of antibiotics in water resources through their release into sewers where they cause bacterial resistance and enhanced drug-resistance in human-borne pathogens and growing microbial populations in the environment. The objective of this study was to investigate the efficiency of  the advanced H2O2/ZnO oxidation process in removing ceftriaxone from aqueous solutions. For this purpose, an experimental study was conducted in which the SEM, XRD, and TEM techniques were employed to determine the size of Zinc oxide nano-particles. Additionally, the oxidation process parameters of pH (3-11, molar ratio of H2O2/ZnO (1.5-3, initial concentration of ceftriaxone (5–15 mg/L, and contact time (30-90 min were investigated. Teh data thus obntained were subjected top statistical analysis using the SPSS (ANOVA test. XRD results revealeda hexagonal crystal structure for the nano-ZnO. TEM images confirmed the spherical shape of the nanoparticles. Finally, SEM images revealed that the Zn nanoparticles used in this study were less than 30 nanometers in diameter. Based on the results, an optimum pH of 11, a contact time of 90 minutes, and a H2O2/ZnO molar ratio equal to 1.5 were the optimum conditions to achieve a ceftriaxone removal efficiency of 92%. The advance H2O2/ZnO oxidation process may thus be claimed to be highly capable of removing ceftriaxone from aqueous solutions.

Scale up of 2,4-dichlorophenol removal from aqueous solutions using Brassica napus hairy roots

Energy Technology Data Exchange (ETDEWEB)

Angelini, Vanina A. [Departamento de Biologia Molecular, FCEFQN, Universidad Nacional de Rio Cuarto, 5800 Rio Cuarto, Cordoba (Argentina); Orejas, Joaquin [Facultad de Ingenieria, Universidad Nacional de Rio Cuarto, 5800 Rio Cuarto, Cordoba (Argentina); Medina, Maria I. [Departamento de Biologia Molecular, FCEFQN, Universidad Nacional de Rio Cuarto, 5800 Rio Cuarto, Cordoba (Argentina); Agostini, Elizabeth, E-mail: eagostini@exa.unrc.edu.ar [Departamento de Biologia Molecular, FCEFQN, Universidad Nacional de Rio Cuarto, 5800 Rio Cuarto, Cordoba (Argentina)

2011-01-15

Research highlights: {yields}B. napus hairy roots were effectively used for a large scale removal of 2,4-DCP. {yields} High removal efficiencies were obtained (98%) in a short time (30 min). {yields} Roots were re-used for six consecutive cycles with high efficiency. {yields} Post removal solutions showed no toxicity. {yields} This method could be used for continuous and safe treatment of phenolic effluents. - Abstract: Chlorophenols are harmful pollutants, frequently found in the effluents of several industries. For this reason, many environmental friendly technologies are being explored for their removal from industrial wastewaters. The aim of the present work was to study the scale up of 2,4-dichlorophenol (2,4-DCP) removal from synthetic wastewater, using Brassica napus hairy roots and H{sub 2}O{sub 2} in a discontinuous stirred tank reactor. We have analyzed some operational conditions, because the scale up of such process was poorly studied. High removal efficiencies were obtained (98%) in a short time (30 min). When roots were re-used for six consecutive cycles, 2,4-DCP removal efficiency decreased from 98 to 86%, in the last cycle. After the removal process, the solutions obtained from the reactor were assessed for their toxicity using an acute test with Lactuca sativa L. seeds. Results suggested that the treated solution was less toxic than the parent solution, because neither inhibition of lettuce germination nor effects in root and hypocotyl lengths were observed. Therefore, we provide evidence that Brassica napus hairy roots could be effectively used to detoxify solutions containing 2,4-DCP and they have considerable potential for a large scale removal of this pollutant. Thus, this study could help to design a method for continuous and safe treatment of effluents containing chlorophenols.

Scale up of 2,4-dichlorophenol removal from aqueous solutions using Brassica napus hairy roots

International Nuclear Information System (INIS)

Angelini, Vanina A.; Orejas, Joaquin; Medina, Maria I.; Agostini, Elizabeth

2011-01-01

Research highlights: →B. napus hairy roots were effectively used for a large scale removal of 2,4-DCP. → High removal efficiencies were obtained (98%) in a short time (30 min). → Roots were re-used for six consecutive cycles with high efficiency. → Post removal solutions showed no toxicity. → This method could be used for continuous and safe treatment of phenolic effluents. - Abstract: Chlorophenols are harmful pollutants, frequently found in the effluents of several industries. For this reason, many environmental friendly technologies are being explored for their removal from industrial wastewaters. The aim of the present work was to study the scale up of 2,4-dichlorophenol (2,4-DCP) removal from synthetic wastewater, using Brassica napus hairy roots and H 2 O 2 in a discontinuous stirred tank reactor. We have analyzed some operational conditions, because the scale up of such process was poorly studied. High removal efficiencies were obtained (98%) in a short time (30 min). When roots were re-used for six consecutive cycles, 2,4-DCP removal efficiency decreased from 98 to 86%, in the last cycle. After the removal process, the solutions obtained from the reactor were assessed for their toxicity using an acute test with Lactuca sativa L. seeds. Results suggested that the treated solution was less toxic than the parent solution, because neither inhibition of lettuce germination nor effects in root and hypocotyl lengths were observed. Therefore, we provide evidence that Brassica napus hairy roots could be effectively used to detoxify solutions containing 2,4-DCP and they have considerable potential for a large scale removal of this pollutant. Thus, this study could help to design a method for continuous and safe treatment of effluents containing chlorophenols.

Removal of Nitrate From Aqueous Solution Using Rice Chaff

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Dehghani

2015-09-01

Full Text Available Background Nitrate is largely dissolved in the surface and ground water, due to its high solubility. Continual uptake of nitrite through drinking water can lead to problems and diseases (such as blue baby for humans, especially children. Objectives The aim of this study was to develop a new and inexpensive method for the removal of nitrate from water. In this regard, the possibility of using chaff for removal of nitrate from aqueous solutions was studied and the optimum operating conditions of nitrate removal was determined. Materials and Methods This is a cross-sectional study conducted in laboratory scale. The UV spectrophotometer at a wavelength of maximum absorbance (220 nm was used to determine the nitrate concentration. The effect of pH, amount of chaff, temperature, and contact time were investigated. Results The result of this study revealed that chaff as an absorbent could remove nitrate from solutions, and the efficiency of adsorption increased as contact time increased from 5 to 30 minutes, amount of chaff increased from 1 to 3 g, temperature increased in a range of 300 - 400°C and the amount of pH decreased from 10 to 3. The maximum adsorption rate was around pH 3 (53.14%. Conclusions It was shown that the removal efficiency of nitrate was directly proportional to the amount of chaff, temperature, and contact time but inversely to the pH. This study showed that nitrate removal by chaff is a promising technique.

Arsenic removal from acidic solutions with biogenic ferric precipitates

Energy Technology Data Exchange (ETDEWEB)

Ahoranta, Sarita H., E-mail: sarita.ahoranta@tut.fi [Department of Chemistry and Bioengineering, Tampere University of Technology, P.O. Box 541, FI-33101 Tampere (Finland); Kokko, Marika E., E-mail: marika.kokko@tut.fi [Department of Chemistry and Bioengineering, Tampere University of Technology, P.O. Box 541, FI-33101 Tampere (Finland); Papirio, Stefano, E-mail: stefano.papirio@unicas.it [Department of Chemistry and Bioengineering, Tampere University of Technology, P.O. Box 541, FI-33101 Tampere (Finland); Özkaya, Bestamin, E-mail: bozkaya@yildiz.edu.tr [Department of Chemistry and Bioengineering, Tampere University of Technology, P.O. Box 541, FI-33101 Tampere (Finland); Department of Environmental Engineering, Yildiz Technical University, Davutpasa Campus 34220, Esenler, Istanbul (Turkey); Puhakka, Jaakko A., E-mail: jaakko.puhakka@tut.fi [Department of Chemistry and Bioengineering, Tampere University of Technology, P.O. Box 541, FI-33101 Tampere (Finland)

2016-04-05

Highlights: • Continuous and rapid arsenic removal with biogenic jarosite was achieved at pH 3.0. • Arsenic removal was inefficient below pH 2.4 due to reduced Fe–As co-precipitation. • As(V) had better sorption characteristics than As(III). • Biogenic jarosite adsorbed arsenic more effectively than synthetic jarosite. - Abstract: Treatment of acidic solution containing 5 g/L of Fe(II) and 10 mg/L of As(III) was studied in a system consisting of a biological fluidized-bed reactor (FBR) for iron oxidation, and a gravity settler for iron precipitation and separation of the ferric precipitates. At pH 3.0 and FBR retention time of 5.7 h, 96–98% of the added Fe(II) precipitated (99.1% of which was jarosite). The highest iron oxidation and precipitation rates were 1070 and 28 mg/L/h, respectively, and were achieved at pH 3.0. Subsequently, the effect of pH on arsenic removal through sorption and/or co-precipitation was examined by gradually decreasing solution pH from 3.0 to 1.6 (feed pH). At pH 3.0, 2.4 and 1.6, the highest arsenic removal efficiencies obtained were 99.5%, 80.1% and 7.1%, respectively. As the system had ferric precipitates in excess, decreased arsenic removal was likely due to reduced co-precipitation at pH < 2.4. As(III) was partially oxidized to As(V) in the system. In shake flask experiments, As(V) sorbed onto jarosite better than As(III). Moreover, the sorption capacity of biogenic jarosite was significantly higher than that of synthetic jarosite. The developed bioprocess simultaneously and efficiently removes iron and arsenic from acidic solutions, indicating potential for mining wastewater treatment.

Comparison of the Efficiency of Simultaneous Application of UV/O3 for the Removal of Organophosphorus and Carbamat Pesticides in Aqueous Solutions

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Mohammad Taghi Samadi

2010-03-01

Full Text Available A vast variety of pesticides are used for agricultural pests in Iran. The release of these persistent organic pollutants. into water supplies leaves adverse effects on both the environment and public health. Advanced oxidation processes have been used recently for pesticide removal. In this research, the combined UV/O3 process has been investigated for the removal of organophosphorus pesticides (Diazinon, Chlorpyrifos, Carbamate pesticides (carbaryl. In this survey, samples have been prepared by adding given concentration (1, 5, 10, 15, 20 mg/L of the pesticides to deionized water. The samples at separation periods were exposed to the combined UV/O3 (UV=50-200 Wm-2 and O3 = 1g hr-1in a bath  reactor at different pH levels (6, 7, 9 and for different contact times (0.5,1,1.5,2 hr and the removal efficiencies were determined. Residual concentrations were determined using GC/MS/MS and HPLC.  Based on the results, increasing pH reduced pesticide concentration and increased contact time had a direct effect on enhancing removal efficiency. The combined UV/O3 process was found to have a high efficiency (>80% in degrading both halogenated Organophosphorus(Chlorpyrifos and non- halogenated Organophosphorus (Diazinon pesticides. Its removal efficiency for degrading carbamate pesticide (Carbari was found to be >90%. Based on our results, this method may be suggested for the removal of pesticides from aqueous solutions.

Potential of Brass to Remove Inorganic Hg(II) from Aqueous Solution through Amalgamation.

Science.gov (United States)

Wenke, Axel; Bollen, Anne; Richard, Jan-Helge; Biester, Harald

2016-06-01

Brass shavings (CuZn45) were tested for their efficiency to remove Hg(II) from contaminated groundwater through amalgamation. The study was focused on long-term retention efficiency, the understanding of the amalgamation process and kinetics, and influences of filter surface alteration. Column tests were performed with brass filters (thickness 3 to 9 cm) flushed with 1000 μg/L Hg solution for 8 hours under different flow rates (300 to 600 mL/h). Brass filters consistently removed >98% of Hg from solution independent of filter thickness and flow rate. In a long-term experiment (filter thickness 2 cm), Hg retention decreased from 96 to 92% within 2000 hours. Batch and column experiments for studying kinetics of Hg removal indicate ~100% Hg removal from solution within only 2 hours. Solid-phase mercury thermo-desorption analysis revealed that Hg(0) diffusion into the brass surface controls kinetics of mercury retention. Brass surface alteration could be observed, but did not influence Hg retention.

Fluoride removal from aqueous solution by pumice: case study on ...

African Journals Online (AJOL)

EJIRO

conditions, the fluoride removal efficiency from Kuhbonan water by 2.8 mg/L fluoride was 74.64%. Eventually ... industrial wastewater containing fluoride is a key ..... solution using silica ceramic: Adsorption kinetics and equilibrium studies.

Investigation of Acorn fruit Ash Efficiency in Cadmium Removal from Aqueous Solutions: Adsorption Isotherm and Kinetic Studies

Directory of Open Access Journals (Sweden)

Salman Zarei

2014-12-01

Full Text Available Background: Heavy metals are known as significant pollutants because of toxicity and nonbiodegradable characteristics. Cadmium is one of the heavy metals that have carcinogen potential. So, this study carried out in order to investigate the acorn fruit ash efficiency in cadmium removal from aqueous solutions. Methods: This study was done in the batch laboratory conditions. In this study, the effect of different parameters including pH, contact time, adsorbent dose, and initial cadmium concentration were evaluated. The Langmuir, Freundlich and Temkin isotherm models were used for analysis of the equilibrium isotherm. Adsorption kinetics of cadmium by different models were also investigated. The measurement of residual cadmium in the samples was determined by atomic absorption spectrophotometry at 228.8 nm. The SPSS-16 software was used for analysis of data. Results: According to the results, the maximum adsorption capacity of cadmium was 9.29 mg/g at pH=7 and 8 g/L adsorbent dose. The removal efficiency was increased with increasing contact time and decreased with increasing of cadmium initial concentration. Investigation of achieving data showed that the adsorption process followed better by Freundlich isotherm and the pseudo-second order kinetic. Conclusions: According to the results of this study, it could be concluded that the acorn fruit ash had high ability in cadmium adsorption and could be used as a cheap adsorbent in the removal of cadmium.

Removal of Methylene Blue from aqueous solution using spent bleaching earth

Science.gov (United States)

Saputra, E.; Saputra, R.; Nugraha, M. W.; Irianty, R. S.; Utama, P. S.

2018-04-01

The waste from industrial textile waste is one of the environmental problems, it is required effective and efficient processing. In this study spent bleaching earth was used as absorbent. It was found that the absorbent was effective to remove methylene blue from aqueous solution with removal efficiency 99.97 % in 120 min. Several parameters such as pH, amount of absorbent loading, stirring speed are found as key factor influencing removal of methylene blue. The mechanism of adsorption was also studied, and it was found that Langmuir isotherm fitted to data of experiment with adsorption capacity 0.5 mg/g.

Storage Duration and Temperature Effects of Strychnos potatorum Stock Solutions on its Coagulation Efficiency

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Rekha R Warrier

2014-12-01

Full Text Available This study presents the effects of storage duration and temperature of Strychnos potatorum stock solution on its coagulation efficiency. Coagulation efficiency of the seed extracts on water samples depended on the initial turbidity of the water sample. The stock solutions could clarify only highly turbid solutions. The optimum dosage of the stock solutions was 5% and optimal time required was 50 minutes. S. potatorum stock solutions, which were kept at room temperature (28 °C, had a shelf life of only five days and were able to remove turbidity from high and low turbidity water samples and no coagulation activity was observed for medium turbidity. The highest turbidity removals were observed for stock solutions, which were kept for three days. For stock solutions which were stored in refrigerator, shelf life was extended upto seven days, and the turbidity removal efficiencies improved from 45.9 to 63.8 for low and 43.7 to 64.9 % for high turbidity water samples, respectively.

The color removal of dye wastewater by magnesium chloride/red mud (MRM) from aqueous solution.

Science.gov (United States)

Wang, Qi; Luan, Zhaokun; Wei, Ning; Li, Jin; Liu, Chengxi

2009-10-30

In this study, the MgCl2/red mud system (MRM) was used to investigate the color removal efficiency of dye solutions. Parameters such as the effect of the dosage of red mud (RM) and MgCl2 have been studied. The effect of pH on the conversion rate of Mg2+ has also been studied. The color removal efficiency of MRM was compared with that of PAC/RM and PAC/NaOH. Meanwhile, the color removal efficiency of RM was compared with that of NaOH. The results show that the MRM system can remove more than 98% of the coloring material at a dosage of 25 g RM/L dye solution and a volume of 1.5 mL MgCl2/L dye solution in the decolorization process of reactive dye, acid dye and direct dye. The color removal efficiency was better than PAC/RM and PAC/NaOH system. The adsorption data have been analyzed using Langmuir and Freundlich isotherms. The results indicated that both models provide the best correlation of the experimental data. The decolorization mechanism of MRM was discussed, too. The MRM system was a viable alternative to some of the more conventional forms of chemical treatment of dye solutions and also provided another way to make use of industrial waste red mud.

Experimental Investigation of Phenanthrene Pollutant Removal Efficiency for Contaminated Sandy Soil by Enhanced Soil Washing

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Saif salah Alquzweeni

2016-12-01

Full Text Available Polycyclic aromatic hydrocarbons (PAHs are environmental concerns that must be removed to acceptable level. This research assesses two agents (Na2EDTA and SDS to remediate contaminated sandy soil, spiked with 500mg/kg phenanthrene. Five sets of experiments (batch are applied to investigate the optimal of five influencing factors on soil remediation: Na2EDTA-SDS concentration, liquid/Solid ratio, stirring speed, pH value of flushing solution and mixing time. The results of batch experiments showed that SDS has high phenanthrene removal efficiency (90%, while Na2EDTA shows no phenanthrene removal. pH has no effect on phenanthrene removal. To study the influence of flow rates on the removal efficiency of contaminants, two column tests with hydraulic gradient of 0.2 and 1.2 conducted by SDS solution. The results illustrate that high phenanthrene removal from soil obtained by 1.2 hydraulic gradient condition. The SDS flushing solution removed approximately 69% and 81% of phenanthrene from soil under low and high hydraulic gradients, respectively. It was concluded that phenanthrene removal depend on surfactant micelles formation. Overall, the study showed that soil flushing removal efficiency for contaminants depends on the flushing agents selectivity and affinity to the contaminants and the condition of hydraulic gradient.

Utilization of poplar wood sawdust for heavy metals removal from model solutions

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Demcak Stefan

2017-06-01

Full Text Available Some kinds of natural organic materials have a potential for removal of heavy metal ions from wastewater. It is well known that cellulosic waste materials or by-products can be used as cheap adsorbents in chemical treatment process. In this paper, poplar wood sawdust were used for removal of Cu(II, Zn(II and Fe(II ions from model solutions with using the static and dynamic adsorption experiments. Infrared spectrometry of poplar wood sawdust confirmed the presence of the functional groups which correspond with hemicelluloses, cellulose and lignin. At static adsorption was achieved approximately of 80 % efficiency for all treated model solutions. Similar efficiency of the adsorption processes was reached after 5 min at dynamic condition. The highest efficiency of Cu(II removal (98 % was observed after 30 min of dynamic adsorption. Changes of pH values confirmed a mechanism of ion exchange on the beginning of the adsorption process.

IODINE REMOVAL EFFICIENCY IN NON-SUBMERGED AND SUBMERGED SELF-PRIMING VENTURI SCRUBBER

OpenAIRE

MAJID ALI; YAN CHANGQI; SUN ZHONGNING; GU HAIFENG; WANG JUNLONG; KHURRAM MEHBOOB

2013-01-01

The objective of this conducted research is to study the iodine removal efficiency in a self-priming venturi scrubber for submerged and non-submerged operating conditions experimentally and theoretically. The alkaline solution is used as an absorbent, which is prepared by dissolving sodium hydroxide (NaOH) and sodium thiosulphate (Na2S2O3) in water to remove the gaseous iodine (I2) from the gas. Iodine removal efficiency is examined at various gas flow rates and inlet concentrations of iodine...

Process for the removal of radium from acidic solutions containing same

Science.gov (United States)

Scheitlin, F.M.

The invention is a process for the removal of radium from acidic aqueous solutions. In one aspect, the invention is a process for removing radium from an inorganic-acid solution. The process comprises contacting the solution with coal fly ash to effect adsorption of the radium on the ash. The radium-containing ash then is separated from the solution. The process is simple, comparatively inexpensive, and efficient. High radium-distribution coefficients are obtained even at room temperature. Coal fly ash is an inexpensive, acid-resistant, high-surface-area material which is available in large quantities throughout the United States. The invention is applicable, for example, to the recovery of /sup 226/Ra from nitric acid solutions which have been used to leach radium from uranium-mill tailings.

Application of Activated Carbon for Removal of Arsenic Ions from Aqueous Solutions

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R. Ansari

2007-01-01

Full Text Available The activated carbon (AC was used for removal of As(III and As(V ions from aqueous solutions. Sorption experiments were conducted using both batch and column systems. The effect of some important parameters on sorption of these by AC was studied. It was found that among the different factors affecting sorption capacity and efficiency in removal of arsenic from aqueous solutions, the effect of pH and the oxidation state were the most prominent. The optimum pH values for removal of As(III and As(V from aqueous solutions using AC was found 12 and 3 respectively. Impregnation of AC with sulphur contain organic dyes, it is possible to improve As(III uptake considerably.

Efficiency of SPIONs functionalized with polyethylene glycol bis(amine) for heavy metal removal

Energy Technology Data Exchange (ETDEWEB)

Wanna, Yongyuth, E-mail: yongyuth.wanna@gmail.com [College of KMITL Nanotechnology, King Mongkut' s Institute of Technology Ladkrabang, Chalongkrung Rd., Ladkrabang, Bangkok 10520 (Thailand); Nara Machinery Co., Ltd., 2-5-7, Jonan-Jima, Ohta-ku, Tokyo 143-0002 (Japan); Chindaduang, Anon; Tumcharern, Gamolwan [National Nanotechnology Center (NANOTEC), 111 Thailand Science Park, Pahol Yothin Rd, Klong Luang, Pathum Thani 12120 (Thailand); Phromyothin, Darinee [College of KMITL Nanotechnology, King Mongkut' s Institute of Technology Ladkrabang, Chalongkrung Rd., Ladkrabang, Bangkok 10520 (Thailand); Porntheerapat, Supanit [NECTEC, National Science and Technology Development Agency (NSTDA), 112 Thailand Science Park, Phahonyothin Rd., Khlong Nueng, Khlong Luang, Pathum Thani 12120 (Thailand); Nukeaw, Jiti [College of KMITL Nanotechnology, King Mongkut' s Institute of Technology Ladkrabang, Chalongkrung Rd., Ladkrabang, Bangkok 10520 (Thailand); Hofmann, Heirich [Laboratory of Powder Technology, Ecole Polytechnique Fédérale de Lausanne (Switzerland); Pratontep, Sirapat [College of KMITL Nanotechnology, King Mongkut' s Institute of Technology Ladkrabang, Chalongkrung Rd., Ladkrabang, Bangkok 10520 (Thailand)

2016-09-15

Hybrid magnetic nanoparticles based on poly(methylmethacrylate) (PMMA) and super-paramagnetic iron oxide nanopaticles (SPIONs) with selective surface modification has been developed for heavy metal removal by applying external magnetic fields. The nanoparticles were prepared by the emulsion polymerization technique in an aqueous suspension of SPIONs. The hydrolysis of carboxyl functional group was then applied for grafting polyethylene glycol bis(amine)(PEG-bis(amine)) onto the PMMA-coated SPIONs. The morphology, the chemical structure and the magnetic properties of the grafted nanoparticles were investigated. The efficiency of the hybrid nanoparticles for heavy metal removal were conducted on Pb(II), Hg(II), Cu(II) and Co(II) in aqueous solutions.The metal concentration in the solutions after separation by the hybrid nanoparticles was determined by inductively coupled plasma optical emission spectrometer (ICP-OES). The results show the heavy metal uptake ratios of 0.08, 0.04, 0.03, and 0.01 mM per gramme of the grafted SPIONs for Pb(II), Hg(II), Cu(II), and Co(II), respectively. A competitive removal of Cu(II), Pb(II), Co(II) and Hg(II) ions in mixed metal salt solutions has also been studied.The heavy metal removal efficiency of the hybrid nanoparitcles was found to depend on the cation radius, in accordance with capture of metal ions by the amine group. - Highlights: • We synthesis hybrid magnetic nanoparticles for heavy metal removal. • The efficiency of hybrid nanoparticles for heavy metal removal is proposed. • We investigated the characteristic of hybrid nanoparticle. • The heavy metal removal efficiency of the hybrid nanoparticle was founded that depend on the heavy metal cation radius.

Cr(VI) removal from aqueous solution by dried activated sludge biomass

International Nuclear Information System (INIS)

Wu Jun; Zhang Hua; He Pinjing; Yao Qian; Shao Liming

2010-01-01

Batch experiments were conducted to remove Cr(VI) from aqueous solution using activated sludge biomass. The effects of acid pretreatment of the biomass, initial pH, biomass and Cr(VI) concentrations on Cr(VI) removal efficiency were investigated. Proton consumption during the removal process and the reducing capacity of sludge biomass were studied. The results show that acid pretreatment could significantly improve Cr(VI) removal efficiency and increase Cr(VI) reducing capacity by 20.4%. Cr(VI) removal was remarkably pH-dependent; lower pH (pH = 1, 2) facilitated Cr(VI) reduction while higher pH (pH = 3, 4) favored sorption of the converted Cr(III). Lower Cr(VI) concentration as well as higher biomass concentration could accelerate Cr(VI) removal. Cr(VI) reduction was not the only reason for proton consumption in the removal process. Pseudo-second-order adsorption kinetic model could successfully simulate Cr(VI) removal except under higher pH conditions (pH = 3, 4).

Efficiency of Dry (Psidium guava) Leaves for The Removal of Cesium-137 from Aqueous Solutions

International Nuclear Information System (INIS)

Omar, H.A.; Abu-Kharda, S.A.; Abd El -Baset, L.A.; Abu-Shohba, R.M.

2012-01-01

Batch experiments for the removal of cesium-137 from aqueous solution onto guava leaves (psidium guava) and carbonized guava leaves were studied as a function of contact time, dosage, ph value and initial concentration ion. The sorption process was described by pseudo first-order, pseudo second-order, Morris and Elovich kinetic models. Cesium concentrations were ranged between 2x10 -5 - 1x10 -3 M. Sorption data have been interpreted in terms of Langmuir, Freundlich and Dubinin-Radushkevich isotherms. The maximum sorption capacity of carbonized guava leaves adsorbent for cesium removal was 8.02 mgg -1 . The results of the present study suggest that carbonized guava leaves can be used beneficially for cesium removal from aqueous solution.

Preparation of magnetic Ni@graphene nanocomposites and efficient removal organic dye under assistance of ultrasound

International Nuclear Information System (INIS)

Zhao, Chuang; Guo, Jianhui; Yang, Qing; Tong, Lei; Zhang, Jingwei; Zhang, Jiwei; Gong, Chunhong; Zhou, Jingfang; Zhang, Zhijun

2015-01-01

Graphical abstract: Reduced graphene oxide/Ni microspheres, being prepared under ultrasound conditions, exhibit a better removal efficiency to decolorize RhB with ultrasonic-assisted decolorization process. - Highlights: • One-step synthesis of Ni@graphene microspheres under ultrasound conditions. • During the ultrasonic process, graphene oxide was reduced and Ni nanoparticles were formed and anchored on graphene sheets. • The products exhibit excellent performance for fast and efficient removal of dye contaminants. • The nanocomposites can be easily separated from solution by a magnet. - Abstract: In this article, we report a facile one-step synthesis of Ni@graphene nanocomposite microspheres (NGs) in hydrazine hydrate solution under ultrasound conditions. During the ultrasonic process, graphene oxide (GO) was reduced effectively under mild conditions and Ni nanoparticles were simultaneously formed and anchored on graphene sheets, which act as spacers to keep the neighboring sheets separated. The target products exhibit excellent performance for fast and efficient removal of dye contaminants, rhodamine B (RhB) in aqueous solution, under assistance of ultrasound. Finally, the nanocomposites can be easily separated from solution by a magnet. Furthermore, higher content of graphene can be produced under sonication, which facilitates faster and more efficient removal of organic contaminates in the solution. The nanocomposites were also characterized by scanning electron microscopy, Raman spectroscopy, Fourier transformed infrared spectroscopy, X-ray photoelectron spectroscopy, X-ray powder diffraction and thermogravimetric analysis.

Preparation of magnetic Ni@graphene nanocomposites and efficient removal organic dye under assistance of ultrasound

Energy Technology Data Exchange (ETDEWEB)

Zhao, Chuang; Guo, Jianhui; Yang, Qing; Tong, Lei [Key Laboratory of Ministry of Education for Special Functional Materials, Henan University, Kaifeng 475004 (China); Zhang, Jingwei, E-mail: jwzhang@henu.edu.cn [Key Laboratory of Ministry of Education for Special Functional Materials, Henan University, Kaifeng 475004 (China); Ian Wark Research Institute, University of South Australia, Mawson Lakes, SA 5095 (Australia); Zhang, Jiwei [Key Laboratory of Ministry of Education for Special Functional Materials, Henan University, Kaifeng 475004 (China); Gong, Chunhong [College of Chemistry and Chemical Engineering, Henan University, Kaifeng 475004 (China); Ian Wark Research Institute, University of South Australia, Mawson Lakes, SA 5095 (Australia); Zhou, Jingfang, E-mail: jingfang.zhou@unisa.edu.au [Ian Wark Research Institute, University of South Australia, Mawson Lakes, SA 5095 (Australia); Zhang, Zhijun [Key Laboratory of Ministry of Education for Special Functional Materials, Henan University, Kaifeng 475004 (China)

2015-12-01

Graphical abstract: Reduced graphene oxide/Ni microspheres, being prepared under ultrasound conditions, exhibit a better removal efficiency to decolorize RhB with ultrasonic-assisted decolorization process. - Highlights: • One-step synthesis of Ni@graphene microspheres under ultrasound conditions. • During the ultrasonic process, graphene oxide was reduced and Ni nanoparticles were formed and anchored on graphene sheets. • The products exhibit excellent performance for fast and efficient removal of dye contaminants. • The nanocomposites can be easily separated from solution by a magnet. - Abstract: In this article, we report a facile one-step synthesis of Ni@graphene nanocomposite microspheres (NGs) in hydrazine hydrate solution under ultrasound conditions. During the ultrasonic process, graphene oxide (GO) was reduced effectively under mild conditions and Ni nanoparticles were simultaneously formed and anchored on graphene sheets, which act as spacers to keep the neighboring sheets separated. The target products exhibit excellent performance for fast and efficient removal of dye contaminants, rhodamine B (RhB) in aqueous solution, under assistance of ultrasound. Finally, the nanocomposites can be easily separated from solution by a magnet. Furthermore, higher content of graphene can be produced under sonication, which facilitates faster and more efficient removal of organic contaminates in the solution. The nanocomposites were also characterized by scanning electron microscopy, Raman spectroscopy, Fourier transformed infrared spectroscopy, X-ray photoelectron spectroscopy, X-ray powder diffraction and thermogravimetric analysis.

Optimizing Electrocoagulation Process for the Removal of Nitrate From Aqueous Solution

Directory of Open Access Journals (Sweden)

Dehghani

2016-01-01

Full Text Available Background High levels of nitrate anion are frequently detected in many groundwater resources in Fars province. Objectives The present study aimed to determine the removal efficiency of nitrate from aqueous solutions by electrocoagulation process using aluminum and iron electrodes. Materials and Methods A laboratory-scale batch reactor was conducted to determine nitrate removal efficiency using the electrocoagulation method. The removal of nitrate was determined at pH levels of 3, 7, and 11, different voltages (15, 20, and 30 V, and operation times of 30, 60, and 75 min, respectively. Data were analyzed using the SPSS software version 16 (Chicago, Illinois, USA and Pearson’s correlation coefficient was used to analyze the relationship between the parameters. Results Results of the present study showed that the removal efficiency was increased from 27% to 86% as pH increased from 3 to 11 at the optimal condition of 30 V and 75 min operation time. Moreover, by increasing the reaction time from 30 V to 75 min the removal efficiency was increased from 63% to 86%, respectively (30 V and pH = 11. Pearson’s correlation analysis showed that there was a significant relationship between removal efficiency and voltage and reaction time as well (P < 0.01. Conclusions In conclusion, the electrocoagulation process can be used for removing nitrate from water resources because of high efficiency, simplicity, and relatively low cost.

Morphology of modified biochar and its potential for phenol removal from aqueous solutions

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Kostas A. Komnitsas

2016-04-01

Full Text Available In the present study, the efficiency of phenol removal from synthetic aqueous solutions by chemically modified biochar with the use of 1M KOH or 1M FeCl3 was investigated. Initially, biochar was produced after slow pyrolysis of three different agricultural wastes, namely pistachio (Pistacia vera L. shells, pecan (Carya illinoinensis shells and wood sawdust. The quality of biochar was assessed by evaluating its main properties, such as pH, surface area, porosity and C content. X-ray diffraction (XRD, Scanning Electron Microscopy (SEM and Fourier Transform Infrared Spectroscopy (FTIR were used for the identification of biochar’s structure. The efficiency of phenol removal from synthetic solutions was assessed with the use of kinetic and equilibrium experiments. The experimental results show that the KOH-modified biochar exhibited the highest phenol removal efficiency. Hydrophobic sorption on its surface is the main phenol removal mechanism. The pseudo-second order model fits best the kinetic data, while the Freundlich model, as deduced from an equilibrium study describes very well sorption of phenols on all biochars examined.

Removal of Phenol in Aqueous Solution Using Kaolin Mineral Clay

International Nuclear Information System (INIS)

Sayed, M.S.

2008-01-01

Kaolin clay were tested for phenol removal as toxic liquid waste from aqueous waste water. Several experimental conditions such as weight and particle size of clay were investigated to study batch kinetic techniques, also the ph and concentration of the phenol solution were carried out. The stability of the Langmuir adsorption model of the equilibrium data were studied for phenol sorbent clay system. Infrared spectra, thermogravimetric and differential thermal analysis techniques were used to characterize the behavior of kaolin clay and kaolin clay saturated with phenol. The results obtained showed that kaolin clay could be used successfully as an efficient sorbent material to remove phenol from aqueous solution

Arsenic Removal from Aqueous Solutions Using Modified and Unmodified Oak Sawdust

Directory of Open Access Journals (Sweden)

Ali Reza Rahmani

2016-01-01

Full Text Available In this research, oak sawdust, in both modified and unmodified forms, was used as an economical and low-cost material for the removal of arsenic from aqueous solutions. For this purpose, arsenic synthetic samples were prepared using NaAsO2 in distilled water and the effects of pH, adsorbent dosage, contact time, and initial As(V concentration were investigated on As(V adsorption using the adsorbents prepared. The results showed that modified sawdust achieved the highest efficiency (>91% over a contact time of 60 min and at pH 7 when the adsorbent dosage was 4gr/L and the initial As(V concentration was 150 µg/L. The data from both adsorbents fitted well to the Langmuir isotherm. Under optimum conditions (an initial As(V concentration of 150 µg/L and optimal absorption pH, contact time, and adsorbent dosage, maximum As(V removal efficiencies were 93.85% and 91.034% with the modified  and unmodified sawdust adsorbents, respectively. Given the availability and low cost of the adsorbent used and the high removal efficiency obtained at  lower adsorbent dosages and contact times, the modified oak sawdust may be recommended as an effective adsorbent for the removal of arsenic (v from aqueous solutions, especially since it requires no need for pH modification.

Survey Efficiency of Ultraviolet and Zinc Oxide Process (UV/ZnO for Removal of Diazinon Pesticide from Aqueous Solution

Directory of Open Access Journals (Sweden)

Mohammad Hadi Dehghani

2015-03-01

Full Text Available The presence of persistent organic pollutants and toxics (e.g., pesticides in ground, surface, and drinking water resources combined with the inability of conventional treatment methods to remove these pollutants have led to the development of advanced oxidation processes. Nowadays, nanophotocatalyst processes are considered as clean and environmentally-friendly treatment methods that can be extensively used for removing contaminants. The objective of the present study was to determine the efficiency of the ultraviolet and zinc oxide (UV/ZnO process in the removal of diazinon pesticide from aqueous solutions. For the purposes of this study, samples were adjusted in a batch reactor at five different detention times. The pH levels used were 3, 7, and 9. Irradiation was performed using a 125 W medium-pressure mercury lamp. The diazinon concentrations of the samples were 100 and 500 µg/L and the concentrations of zinc oxide nanoparticles were 50, 100, and 150 mg/L. The highest degradation efficiency was observed at pH 7 (mean = 80.92 30.3, while the lowest was observed for pH 3 (mean 67.11 24.49. Results showed that the optimal concentration of nanoparticles (6-12 nm was 100 mg L-1.

Electrochemical removal of indium ions from aqueous solution using iron electrodes

International Nuclear Information System (INIS)

Chou, Wei-Lung; Huang, Yen-Hsiang

2009-01-01

The removal of indium ions from aqueous solution was carried out by electrocoagulation in batch mode using an iron electrode. Various operating parameters that could potentially affect the removal efficiency were investigated, including the current density, pH variation, supporting electrolyte, initial concentration, and temperature. The optimum current density, supporting electrolyte concentration, and temperature were found to be 6.4 mA/cm 2 , 0.003N NaCl, and 298 K, respectively. When the pH values lower than 6.1, the removal efficiencies of indium ions via electrocoagulation were up to 5 times greater than those by adding sodium hydroxide. The indium ion removal efficiency decreased with an increase in the initial concentration. Results for the indium ion removal kinetics at various current densities show that the kinetic rates conformed to the pseudo-second-order kinetic model with good correlation. The experimental data were also tested against different adsorption isotherm models for describing the electrocoagulation process. The adsorption of indium ions preferably fitting the Langmuir adsorption isotherm suggests monolayer coverage of adsorbed molecules.

Electrochemical removal of indium ions from aqueous solution using iron electrodes

Energy Technology Data Exchange (ETDEWEB)

Chou, Wei-Lung, E-mail: wlchou@sunrise.hk.edu.tw [Department of Safety, Health and Environmental Engineering, Hungkuang University, No. 34 Chung-Chie Road, Sha-Lu, Taichung 433, Taiwan (China); Huang, Yen-Hsiang [Department of Safety, Health and Environmental Engineering, Hungkuang University, No. 34 Chung-Chie Road, Sha-Lu, Taichung 433, Taiwan (China)

2009-12-15

The removal of indium ions from aqueous solution was carried out by electrocoagulation in batch mode using an iron electrode. Various operating parameters that could potentially affect the removal efficiency were investigated, including the current density, pH variation, supporting electrolyte, initial concentration, and temperature. The optimum current density, supporting electrolyte concentration, and temperature were found to be 6.4 mA/cm{sup 2}, 0.003N NaCl, and 298 K, respectively. When the pH values lower than 6.1, the removal efficiencies of indium ions via electrocoagulation were up to 5 times greater than those by adding sodium hydroxide. The indium ion removal efficiency decreased with an increase in the initial concentration. Results for the indium ion removal kinetics at various current densities show that the kinetic rates conformed to the pseudo-second-order kinetic model with good correlation. The experimental data were also tested against different adsorption isotherm models for describing the electrocoagulation process. The adsorption of indium ions preferably fitting the Langmuir adsorption isotherm suggests monolayer coverage of adsorbed molecules.

A study on removal of elemental mercury in flue gas using fenton solution

International Nuclear Information System (INIS)

Liu, Yangxian; Wang, Yan; Wang, Qian; Pan, Jianfeng; Zhang, Yongchun; Zhou, Jianfei; Zhang, Jun

2015-01-01

Highlights: • A novel technique on oxidation of Hg 0 using Fenton was proposed. • The effects of several process parameters on Hg 0 removal were studied. • Products and ·OH in solution were detected. • Reaction mechanism of Hg 0 removal was studied. • Simultaneous removal of Hg 0 , NO and SO 2 was also studied. - Abstract: A novel technique on oxidation-separation of elemental mercury (Hg 0 ) in flue gas using Fenton solution in a bubbling reactor was proposed. The effects of several process parameters (H 2 O 2 concentration, Hg 0 inlet concentration, Fe 2+ concentration, solution temperature, solution pH, gas flow) and several flue gas components (NO, SO 2 , O 2 , CO 2 , inorganic ions and particulate matters on Hg 0 removal were studied. The results indicate that H 2 O 2 concentration, Fe 2+ concentration, solution pH and gas flow have great effects on Hg 0 removal. Solution temperature, Hg 0 , NO, SO 2 , CO 3 2− and HCO 3 − concentrations also have significant effects on Hg 0 removal. However, Cl − , SO 4 2− , NO 3 − , O 2 and CO 2 concentrations only have slight effects on Hg 0 removal. Furthermore, reaction mechanism of Hg 0 removal and simultaneous removal process of Hg 0 , NO and SO 2 were also studied. Hg 0 is removed by oxidation of ·OH and oxidation of H 2 O 2 . The simultaneous removal efficiencies of 100% for SO 2 , 100% for Hg 0 and 88.3% for NO were obtained under optimal test conditions. The results demonstrated the feasibility of Hg 0 removal and simultaneous removal of Hg 0 , SO 2 and NO using Fenton solution in a bubbling reactor

Electrocoagulation-Adsorption to Remove Anionic and Cationic Dyes from Aqueous Solution by PV-Energy

OpenAIRE

Castañeda-Díaz, J.; Pavón-Silva, T.; Gutiérrez-Segura, E.; Colín-Cruz, A.

2017-01-01

The cationic dye malachite green (MG) and the anionic dye Remazol yellow (RY) were removed from aqueous solutions using electrocoagulation-adsorption processes. Batch and continuous electrocoagulation procedures were performed and compared. Carbonaceous materials obtained from industrial sewage sludge and commercial activated carbons were used to adsorb dyes from aqueous solutions in column systems with a 96–98% removal efficiency. The continuous electrocoagulation-adsorption system was more ...

Arsenic removal from acidic solutions with biogenic ferric precipitates.

Science.gov (United States)

Ahoranta, Sarita H; Kokko, Marika E; Papirio, Stefano; Özkaya, Bestamin; Puhakka, Jaakko A

2016-04-05

Treatment of acidic solution containing 5g/L of Fe(II) and 10mg/L of As(III) was studied in a system consisting of a biological fluidized-bed reactor (FBR) for iron oxidation, and a gravity settler for iron precipitation and separation of the ferric precipitates. At pH 3.0 and FBR retention time of 5.7h, 96-98% of the added Fe(II) precipitated (99.1% of which was jarosite). The highest iron oxidation and precipitation rates were 1070 and 28mg/L/h, respectively, and were achieved at pH 3.0. Subsequently, the effect of pH on arsenic removal through sorption and/or co-precipitation was examined by gradually decreasing solution pH from 3.0 to 1.6 (feed pH). At pH 3.0, 2.4 and 1.6, the highest arsenic removal efficiencies obtained were 99.5%, 80.1% and 7.1%, respectively. As the system had ferric precipitates in excess, decreased arsenic removal was likely due to reduced co-precipitation at pHremoves iron and arsenic from acidic solutions, indicating potential for mining wastewater treatment. Copyright © 2015 Elsevier B.V. All rights reserved.

Removal of phenol from aqueous solution using rice straw as adsorbent

Science.gov (United States)

Sarker, Nandita; Fakhruddin, A. N. M.

2017-06-01

Phenol is an environmental pollutant; the present study was conducted to examine the adsorption of phenol by rice straw. For this purpose raw (untreated), physically treated (boiled and dried) and thermally treated (heated at 230 °C for 3 h to produce ash) rice straw were selected to determine phenol removal efficiency at different contact times and adsorbent dosages for 1 and Percentage of removal of phenol increased as the adsorbent dose increase. The removal efficiency increase in the order of: raw rice straw ash) rice straw. Langmuir and Freundlich isotherm was developed for 1 and ash) treated rice straw. Freundlich isotherm best fit the equilibrium data for 1 mm thermally treated rice straw. The results showed that thermally treated rice straw (ash) can be developed as a potential adsorbent for phenol removal from aqueous solution.

A new nano-sorbent for fast and efficient removal of heavy metals from aqueous solutions based on modification of magnetic mesoporous silica nanospheres

Science.gov (United States)

Vojoudi, Hossein; Badiei, Alireza; Bahar, Shahriyar; Mohammadi Ziarani, Ghodsi; Faridbod, Farnoush; Ganjali, Mohammad Reza

2017-11-01

In the present study, a new and efficient nanosorbent for the fast removal of heavy metal ions was prepared. The proposed nanosorbent was fabricated using Fe3O4 magnetic core shelled by mesoporous silica, and cetyltrimethylammonium bromide (CTAB) as surfactant template through a sol-gel process. The magnetic nanomaterial was further modified with bis(3-triethoxysilylpropyl)tetrasulfide (MSCMNPs-S4). The final nanosphers were characterized by FT-IR, XRD, TGA, BET, SEM, TEM, DLS, VSM, EDX, and UV-Vis. The potential of the resultant mesoporous magnetite nanomaterials was investigated as a convenient and effective adsorbent for the removal of toxic heavy metal ions from aqueous solutions in a batch system. The effect of essential parameters on the removal efficiency including initial pH of sample solution, adsorbent amount, metal ion concentration, contact time and type and quantity of the eluent on the adsorption characteristics of the MSCMNPs-S4 were studied. Under the optimized conditions, the proposed nanosorbent exhibited high adsorption capacity of 303.03, 256.41 and 270.27 mg g-1 and maximum removal percentages of 98.8%, 96.4%, 95.7% for Hg(II), Pd(II) and Pb(II) ions, respectively. The mechanism of the adsorbtion was found to be in good agreement with the Langmuir isotherm model. Furthermore, the reusability investigation indicated that the MSCMNPs-S4 could be used frequently at least for five cycles without any significant loss in its performance.

Investigation of Pb(II Removal from Aqueous Solutions Using Modified Nano Zero-Valent Iron Particles

Directory of Open Access Journals (Sweden)

Amirhossein Ramezanpoor

2014-05-01

Full Text Available This research was conducted in experimental scale with the aim of investigation effect of polyacrylic acid-stabilized zero-valent iron nanoparticles (PAA-nZVI on lead removal from aqueous solution. In this regards, NZVI was synthesized with polyacrylic acid and their size and morphological characteristics were examined via X-ray diffraction (XRD, Scanning Electron Microscopy (SEM and Fourier Transmission Infrared Spectroscopy (FTIR. To study the effect of PAA-nZVI on lead removal, pH of aqueous solution, contact time, PAA-NZVI concentration  and initial Pb(II concentration were considered as variables. Furthermore, the experimental data of Pb(II  removal were fitted using three kinetic models, namely Zero-order, First-order and Second-order.The results of experiments showed that maximum Pb(II removal efficiency was observed at pH=5, 15 min contact time and 5 g/L PAA-nZVI concentration. Moreover, the results of kinetic studies indicated that among all applied kinetic models, First-order kinetic model had more better prediction than other kinetic models ofPb(II removal. Based on the results of present research, PAA-NZVI is an efficient agent to remove Pb(II from aqueous solutions.

Boron removal from aqueous solutions by activated carbon impregnated with salicylic acid

International Nuclear Information System (INIS)

Celik, Z. Ceylan; Can, B.Z.; Kocakerim, M. Muhtar

2008-01-01

In this study, the removal of boric acid from aqueous solution by activated carbon impregnated with salicylic acid was studied in batch system. pH, adsorbent amount, initial boron concentration, temperature, shaking rate and salicylic acid film thickness were chosen as parameters. Boron removal efficiencies increased with increasing adsorbent amount, temperature and pH, decreasing initial boron concentration. As thickness of salicylic acid film on activated carbon becomes thin up to 0.088 nm, the efficiency increased, and then, the efficiency decreased with becoming thinner than 0.088 nm of salicylic acid film. Shaking rate was no effect on removal efficiency. In result, it was determined that the use of salicylic acid as an impregnant for activated carbon led to the increase of the amount of boron adsorbed. A lactone ring, being the most appropriate conformation, forms between boric acid and -COOH and -OH groups of salicylic acid

Boron removal from aqueous solutions by activated carbon impregnated with salicylic acid

Energy Technology Data Exchange (ETDEWEB)

Celik, Z. Ceylan [Department of Environmental Engineering, Atatuerk University, Faculty of Engineering, Erzurum (Turkey)], E-mail: zcelik@atauni.edu.tr; Can, B.Z. [Department of Environmental Engineering, Atatuerk University, Faculty of Engineering, Erzurum (Turkey); Kocakerim, M. Muhtar [Department of Chemical Engineering, Atatuerk University, Faculty of Engineering, 25240 Erzurum (Turkey)

2008-03-21

In this study, the removal of boric acid from aqueous solution by activated carbon impregnated with salicylic acid was studied in batch system. pH, adsorbent amount, initial boron concentration, temperature, shaking rate and salicylic acid film thickness were chosen as parameters. Boron removal efficiencies increased with increasing adsorbent amount, temperature and pH, decreasing initial boron concentration. As thickness of salicylic acid film on activated carbon becomes thin up to 0.088 nm, the efficiency increased, and then, the efficiency decreased with becoming thinner than 0.088 nm of salicylic acid film. Shaking rate was no effect on removal efficiency. In result, it was determined that the use of salicylic acid as an impregnant for activated carbon led to the increase of the amount of boron adsorbed. A lactone ring, being the most appropriate conformation, forms between boric acid and -COOH and -OH groups of salicylic acid.

Feasibility of Cr (VI Removal from Aqueous Solution Using Electrochemical Bipolar Aluminum Electrodes

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Abbas Rezaei

2013-08-01

Full Text Available Electrocoagulation is one of the technologies which have been considered by many researchers in recent years. This process has many advantages including high efficiency, no need to chemical addition, low sludge production, capability of process control, easy to operation and maintenance. Bipolar electrodes system is one of the electrocoagulation techniques which can be used for increasing the process efficiency and better distribution of the electric current. The aim of this study was to remove hexavalent chromium from aqueous solution by electrocoagulation technique. Response surface methodology (RSM was used to optimize the parameters involving in the process, and the effect of current density, initial chromium concentration and pH on the process were investigated. At optimal conditions, for the highest chromium removal (>90%, the optimum initial chromium, reaction time, current density and pH were found to be 117 mg/L, 50 min, 11.75 mA cm-2 and 4.5, respectively. It can be stated that electrocoagulation is an efficient technique for separation and removing high chromium concentration from aqueous solutions.

Evaluation of Iron and Manganese-Coated Pumice Application for the Removal of as(v from Aqueous Solutions

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Leila Babaie Far

2012-12-01

Full Text Available Arsenic contamination of water has been recognized as a serious environmental issue and there are reports on its epidemiological problems to human health. The objective of this study was to evaluate the performances of iron-coated pumice and manganese-coated pumice as the adsorbents for removing arsenate from aqueous solutions. The effect of various parameters such as adsorbent dose, contact time, pH and initial concentration on removal efficiency of arsenate were evaluated in batch mode. The data obtained from the kinetic studies were analyzed using kinetic models of pseudo-first-order and pseudo-second-order. In addition, two isotherm models of Freundlich and Langmuir were used to fit the experimental data. The results showed that the optimum dosage of iron-coated pumice and manganese-coated pumice for arsenate removal were 40 and 80 g/L whereas the adsorption process reached equilibrium after 80 and 100 min, respectively. The maximum removal efficiency of arsenate using the two adsorbents were both recorded in pH=3 as the removal efficiency gradually declinedfollowing every increase in pH values of the solution. Iron-coated pumice also showed to have high removal efficiency when the initial concentration of arsenate was high while the low concentration of arsenate was efficiently removed by manganese-coated pumice. Moreover, it was depicted that the adsorption kinetics by bothadsorbents followed pseudo-second order equation and the uptake data of arsenate were well fitted with Langmuir isotherm model. Therefore, it could be concluded that iron and manganese-coated pumice could beconsidered as suitable adsorbents for arsenate removal from aqueous solutions.

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

Science.gov (United States)

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

2008-02-11

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

Investigation of Phenol Removal by Proxy-Electrocoagulation Process with Iron Electrodes from Aqueous Solutions

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Ali Assadi

2017-09-01

Full Text Available Background: Phenol as an aromatic hydroxyl compound are considered as a priority pollutant. Because of their stability, solubility in water and high toxicity had health important. Methods: In the present experimental study, electrocoagulation reactor by iron electrodes are used in the presence of hydrogen peroxide to phenol removing from aqueous solutions. Effects of variables including H2O2 dosage, reaction time, pH, current density and initial phenol concentration were evaluated to estimate the efficiency of the process. Results: The results showed that pH and H2O2 have the most important role in the removal of phenol. Increasing of H2O2 concentrations from 0.0125 to 0.025 M increased removal efficiency from 74% to 100%. Maximum removal was achieved at pH=3. However, increasing the pH to 9 lead to reducing removal efficiency to 9.8%. Also, by increasing of current density removal efficiency was increased. But with increasing initial concentration of phenol removal efficiency was reduced. Conclusion: Proxy-electrocoagulation process as an effective and robust process can be used for handling of phenol containing wastewater.

A study on removal of elemental mercury in flue gas using fenton solution

Energy Technology Data Exchange (ETDEWEB)

Liu, Yangxian; Wang, Yan; Wang, Qian; Pan, Jianfeng [School of Energy and Power Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013 (China); Zhang, Yongchun [Jiangsu Province Special Equipment Safety Supervision Inspection Institute (Branch of Wuxi), Wuxi 214000 (China); Zhou, Jianfei [School of Energy and Power Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013 (China); Zhang, Jun [Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education, Southeast University, Nanjing 210096 (China)

2015-07-15

Highlights: • A novel technique on oxidation of Hg{sup 0} using Fenton was proposed. • The effects of several process parameters on Hg{sup 0} removal were studied. • Products and ·OH in solution were detected. • Reaction mechanism of Hg{sup 0} removal was studied. • Simultaneous removal of Hg{sup 0}, NO and SO{sub 2} was also studied. - Abstract: A novel technique on oxidation-separation of elemental mercury (Hg{sup 0}) in flue gas using Fenton solution in a bubbling reactor was proposed. The effects of several process parameters (H{sub 2}O{sub 2} concentration, Hg{sup 0} inlet concentration, Fe{sup 2+} concentration, solution temperature, solution pH, gas flow) and several flue gas components (NO, SO{sub 2}, O{sub 2}, CO{sub 2}, inorganic ions and particulate matters on Hg{sup 0} removal were studied. The results indicate that H{sub 2}O{sub 2} concentration, Fe{sup 2+} concentration, solution pH and gas flow have great effects on Hg{sup 0} removal. Solution temperature, Hg{sup 0}, NO, SO{sub 2}, CO{sub 3}{sup 2−} and HCO{sub 3}{sup −} concentrations also have significant effects on Hg{sup 0} removal. However, Cl{sup −}, SO{sub 4}{sup 2−}, NO{sub 3}{sup −}, O{sub 2} and CO{sub 2} concentrations only have slight effects on Hg{sup 0} removal. Furthermore, reaction mechanism of Hg{sup 0} removal and simultaneous removal process of Hg{sup 0}, NO and SO{sub 2} were also studied. Hg{sup 0} is removed by oxidation of ·OH and oxidation of H{sub 2}O{sub 2}. The simultaneous removal efficiencies of 100% for SO{sub 2}, 100% for Hg{sup 0} and 88.3% for NO were obtained under optimal test conditions. The results demonstrated the feasibility of Hg{sup 0} removal and simultaneous removal of Hg{sup 0}, SO{sub 2} and NO using Fenton solution in a bubbling reactor.

EFFICIENCY OF DOMESTIC REVERSE OSMOSIS IN REMOVAL OF TRIHALOMETHANES FROM DRINKING WATER

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S. Mazloomi ، R. Nabizadeh ، S. Nasseri ، K. Naddafi ، S. Nazmara ، A. H. Mahvi

2009-10-01

Full Text Available The reaction of disinfectants with natural organic matters existing in water lead to the formation of Disinfection By-Products. Potentially hazardous and carcinogenic characteristics of trihalomethanes (THMs are recognized. Thus removal of THMs or its precursors are necessary for human health. The aim of this study was to study the efficiency of domestic reverse osmosis (RO in removal of trihalomethanes from drinking water. A pilot scale of RO system with Polyamide membrane as Spiral-Wound, Tape wrapping module was used. Feed solution was made by using of pure chloroform. The samples containing chloroform were analyzed using a gas chromatograph equipped with a flame ionization detector. By increasing the flow, the removal rate of chloroform decreased and with declining removal of EC, the removal of chloroform declined too. In this research, at the worst condition, the efficiency of the pilot scale reverse osmosis reached to 80 % removal of chloroform.

Removal of Nickel from Aqueous Solution by Hard-Shell Pistachios

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Shayan Shamohammadi

2013-08-01

Full Text Available Nickel is one of the heavy metals which commonly can be found in industrial wastewater. Many studies have been done on agricultural waste for the removal of nickel from aqueous solutions. The purpose of this study is to identify hard-shell pistachios as a local attraction for removal of nickel from aqueous solution. Nickel adsorption isotherm models are studied using shell pistachios. Pistachio shell was chosen which its particle size is between 800-600 microns. The stock solution of nickel ions was prepared mixing nickel nitrate with distilled water. The results showed that the maximum absorption efficiency occurs (73.3% at pH=8. Also, it was shown that with increasing adsorbent dose, equilibrium time decreased within constant concentration. Examination of uptake isotherm models showed that models of Freundlich, BET, Radke-Praunitz, Redlich-Peterson and Sips describe data in 97% level of confidence well,  however Freundlich and Sips isotherm models has the lowest error factor 0.10597 and 0/10598 respectively and the highest correlation coefficient (0.9785. Comparison of adsorbent capacity within removal of nickel from aqueous solution shows that Pistachio shell with special absorbent surface of 1.7 m2/g and uptake capacity of 0.3984 mg/g is proper than adsorbents of Kaolinite, Bagasse, sludge-ash.

Using Eggshell in Acid Orange 2 Dye Removal from Aqueous Solution

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Ahmad Reza Yari

2015-05-01

Full Text Available Background and purpose: Generated dye wastewater by the textile industry is usually toxic, non-biodegradable and resistant in the environment. Eggshell is one of the inexpensive material and for the reason the vesicular structures can be used as a proper adsorbent for pollutants removal. The aim of this study is to investigate the efficiency of eggshell for removal of acid orange 2 dye from aqueous solution. Materials and Methods: In the experimental study was determined the efficacy of variant variables such as contact time (15, 30, 60, 90 and 120 min, pH (3, 7 and 11, adsorbent dose (10, 25, 50 and 75 g/L, and initial dye concentration (25, 50 and 100 mg/L. The concentration of dye by spectrophotometer ultraviolet/visible in the wavelength 483 nm was examined. Results: The results showed that with increasing contact time and adsorbent dose, the dye removal efficiency was increased, but with increasing pH and initial dye concentration the removal efficiency was decreased. The maximum of removal efficiency of acid orange 2 dye got in the optimum pH: 3, contact time: 90 min, adsorbent dose: 50 g/L and initial dye concentration: 25 mg/L. Adsorption of acid orange 2 dye (R2 = 0.87 follow the Freundlich isotherm. Conclusion: Eggshells can be used as an inexpensive and effective adsorbent for the removal of acid orange 2 dye.

Evaluation of BTEX and phenol removal from aqueous solution by multi-solute adsorption onto smectite organoclay.

Science.gov (United States)

Carvalho, M N; da Motta, M; Benachour, M; Sales, D C S; Abreu, C A M

2012-11-15

The removal process of BTEX and phenol was evaluated. The smectite organoclay for single-solute system reached removal was evaluated by adsorption on smectite organoclay adsorbent by kinetic and equilibrium efficiencies between 55 and 90% while was reached between 30 and 90% for multi-solute system at 297 K and pH 9. The Langmuir-Freundlich model was used to fit the experimental data with correlation coefficient between 0.98 and 0.99 providing kinetic and equilibrium parameter values. Phenol and ethylbenzene presented high maximum adsorbed amount, 8.28 and 6.67 mg/g, respectively, compared to the other compounds for single-solute. Toluene and p-xylene presented high values of adsorption constant which indicates a high adsorption affinity of compounds to organoclay surface and high binding energy of adsorption. Phenol presented low kinetic adsorption constant value indicating slow rate of adsorption. Copyright © 2012 Elsevier B.V. All rights reserved.

Removal of Pb2+ from aqueous solutions by a high-efficiency resin

International Nuclear Information System (INIS)

Guo, Hao; Ren, Yongzheng; Sun, Xueliang; Xu, Yadi; Li, Xuemei; Zhang, Tiancheng; Kang, Jianxiong; Liu, Dongqi

2013-01-01

The removal of Pb 2+ from aqueous solution by 732 cation-exchange resin in sodium type (732-CR) has been studied in batch experiments at varying pH (2.0–8.0), Pb 2+ concentration (50–200 mg/L), contact time (5–300 min), temperature (288–308 K) and resin dose (0.125–0.75 g/L). The experimental data show that the ion-exchange process was dependent on pH and temperature, the optimal exchange capacity was found at pH 4.0, and higher temperature was beneficial to lead sorption. Kinetic data indicate that the ion-exchange process followed a pseudo-first order model. The equilibrium exchange capacity could be reached at approximately 4 h, and the maximum sorption capacity of Pb 2+ at pH 4.0 was 396.8 mg/g resin. The equilibrium data were evaluated with Langmuir and Freundlich model, and were best fitted with Langmuir model. The thermodynamic parameters for removal of Pb 2+ indicate that the reaction was spontaneous and endothermic. Additionally, column tests were conducted by using both synthetic solution and effluents from lead battery industry. The regeneration of resin was performed for two sorption-regeneration cycles by 1 M NaOH, and the results show that effective regeneration was achieved by this method.

The Application of Low-Cost Adsorbent for Reactive Blue 19 Dye Removal from Aqueous Solution: Lemna Minor

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Davoud Balarak

2015-10-01

Full Text Available Background & Aims of the Study: Due to widespread use and adverse effect of dyes, the removal of dyes from effluents is necessary. This study was aimed to remove the reactive blue 19 dye removal from aqueous solution by dried Lemna minor. Materials and Methods:  The effect of various parameters including contact time, solution pH, adsorbent dosage and dye concentration was investigated in this experimental-lab study, Also, the isotherm and kinetic studies was performed for RB19 dye adsorption process. Results: The results indicated that RB19 dye removal efficiency increases by increasing of contact time and adsorbent dosage. The equilibrium time was 75 min ad the maximum dye removal efficiency was obtained in pH=3. Also, the dye removal efficiency decreases by increasing of pH and initial concentration. It was found that the equilibrium data was best follow by Langmuier isotherm. Also, the pseudo-second-kinetic model was best applicable for RB 19 dye adsorption. Conclusion: It can be concluded that the dried Lemna minor can be considered as an effective adsorbent to remove the RB19 dye.

Removal efficiency of methylene blue using activated carbon from waste banana stem: Study on pH influence

Science.gov (United States)

Misran, E.; Bani, O.; Situmeang, E. M.; Purba, A. S.

2018-02-01

The effort to remove methylene blue in artificial solution had been conducted using adsorption process. The abundant banana stem waste was utilized as activated carbon precursor. This study aimed to analyse the influence of solution pH to removal efficiency of methylene blue using activated carbon from banana stem as adsorbent. Activated carbon from banana stem was obtained by chemical activation using H3PO4 solution. Proximate analysis result showed that the activated carbon has 47.22% of fixed carbon. This value exhibited that banana stem was a potential adsorbent precursor. Methylene blue solutions were prepared at initial concentration of 50 ppm. The influence of solution pH was investigated with the use of 0.2 g adsorbent for 100 mL dye solution. The adsorption was conducted using shaker with at a constant rate of 100 rpm at room temperature for 90 minutes. The results showed that solution pH influenced the adsorption. The activated carbon from banana stem demonstrated satisfying performance since removal efficiencies of methylene blue were higher than 99%.

Removal of fission products from waste solutions using 16 different soil samples

International Nuclear Information System (INIS)

Bangash, M.A.; Hanif, J.

1997-01-01

Most of the nuclear sites use pits in the surrounding soils for the storage/disposal of low active waste (LAW) solutions. The characteristics of the soil if not suitable for the fixation or adsorption of the radioactive nuclides, may cause migration of these nuclides to hydrosphere. The phenomenon has the risk of radio toxic pollution for the living bodies therefore minerals composing the soil and their adsorption properties need to be investigated. For this purpose 16 different soil samples were collected from all over Pakistan. Mineralogical composition of the soils was determined by X-ray diffraction analysis. It was found that most of the samples contained clay minerals, illite, kaolinite and montmorillonite. Studies for the removal of fission products like, /sup 137/Cs. /sup 60/Sr and activation product /sup 60/CO from solution were carried out on these samples. The sorption experiments were performed by batch technique using radioactive as tracers. Distribution co-efficient were determined by mixing he element solution at pH 3 with the soil at soil solution ratios of 1 to 20. It is revealed from the experimental data that efficient removal of fission products from solutions is achieved by soil samples containing clay mineral montmorillonite, followed by little and kaolinite. These soils thus can be effectively used for the disposal of low level radioactive waste solutions without causing any environmental hazard. (author)

Application of Azolla for 2, 4, 6-Trichlorophenol (TCP Removal from Aqueous Solutions

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Mohammad Ali Zazouli

2013-11-01

Full Text Available Background & Aims of the Study: The 2, 4, 6-Trichlorophenol (TCP is a phenolic compound which it can produce adverse effects on human and environment. Therefore, the removal of these compounds is necessary. The aim of this study is the investigation of TCP removal by using Azolla filiculoides biomass. Materials & Methods: The Azolla biomass was dried in the sunlight, and then it was crushed and sieved to particle sizes in range of 1-2 mm. Next treated with 0.1M HCl for a period of 5h. The Azolla was washed with distilled water and it was used as adsorbent. The effect of operating parameters such as pH, contact time, TCP concentration and adsorbent dose on the TCP removal efficiency was investigated. The residues concentration of TCP was measured by spectrophotometer in λ max of 296 nm. Results: In optimum condition (pH 3, contact time 120 min , adsorbent dose 10 gr/l and TCP concentration 10 ppm, Azolla was able to remove 95% of TCP from aqueous solutions. The equilibrium data follows the Langmuir isotherm and the proper kinetic model is pseudo-second model. Conclusions: Adsorption process by Azolla filiculoides is an efficient method for removal of 2, 4, 6-Trichlorophenol from aqueous solutions.

Effects of operational parameters on the removal of brilliant green dye from aqueous solutions by electrocoagulation

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Barun Kumar Nandi

2017-05-01

Full Text Available This paper presents an experimental study on the removal of brilliant green dye from aqueous solutions in a batch stirred electrocoagulation (EC reactor using iron electrodes. The main objectives of the experiments were to investigate the effects of the various operating parameters, such as current density, inter electrode distance, initial dye concentration, pH of the solution, EC duration and salt (NaCl concentrations on the brilliant green dye removal efficiency from synthetic wastewater containing in batch EC process. The experimental results showed that 99.59% dye removal was observed for initial dye concentration of 100 mg/L with current density of 41.7 A/m2, initial pH of 4.0 at the end of 30 min of operation. It was observed that, an increase in current density, time of operation and decrease in inter electrode distance improved the dye removal efficiency. Optimum pH for highest dye removal was 4.0–10.0. It was also observed that increase in salt (NaCl concentration in the solution reduces the specific electrical energy consumption (SEEC.

Removal of strontium ions from solutions using granulated zeolites

International Nuclear Information System (INIS)

Bronic, J.; Subotic, B.

1992-01-01

The ion-exchange process on columns filled with granulated zeolites is determined by several physico-chemical parameters. The influence of these parameters (zeolite type, concentration of exchangeable ions in solution, temperature, flow rate, etc.) on the kinetics of ion-exchange process was studied by measuring the Sr 2+ ion concentration in solution before and after passing through a column filled with various granulated zeolites (zeolite 13X, zeolite A and synthetic mordenite). Using the experimental technique of radioactive labeling by 89 Sr, the distribution of Sr 2+ ions in column fillings were also determined. From the results obtained, the optimal conditions for the most efficient removal of strontium ions from solutions using granulated zeolites can be defined. (author) 24 refs.; 9 figs

Removal of phenol from radioactive waste solutions using activated granular Carbon and activated vermiculite

International Nuclear Information System (INIS)

Ezz El-Din, M.R.; Atta, E.R.

2006-01-01

The efficiency of both activated granular carbon (AGC) and activated vermiculite (AV) in removal of phenol from aqueous waste solutions is of great interest. The aim of the present study is to compare the absorbance capacities of both AGC and AV for the removal of phenol from radioactive waste solutions and to identify the factors affecting the sorption process. The experimental results were in the form of batch sorption measurements for the removal of phenol at ambient temperature (29 ± 1 degree C) and for times up to 40 min and 180 min for AGC and AV, respectively. The results indicated that activated carbon has good efficiency to adsorb phenol. Freundlich equation has been fitted to both AGC and AV for the contaminant removal. The adsorption capacities of both AGC and AV to phenol were 17.4 mg g-1 and 4.5 mg g-1, respectively. The maximum desorption percent of phenol from both loaded AGC and loaded AV were 9 % and 0 %, respectively, and it attained within about 200 min. accordingly, it is recommended that activated carbon is preferred in the applied field for removing phenol from radioactive aqueous wastes

Evaluation of the efficiency of denture cleaners for removing denture adhesives.

Science.gov (United States)

Harada-Hada, Kae; Hong, Guang; Abekura, Hitoshi; Murata, Hiroshi

2016-12-01

We developed a new scoring index for assessing the removability of denture adhesives and evaluated the removal efficiency of denture cleaners. Although our understanding of the importance of denture care is increasing, little is known about the effectiveness and efficiency of denture cleaners on denture adhesives. Therefore, guidelines for proper cleaning are necessary. We used five denture cleaner solutions on two cream adhesives, one powder adhesive and one cushion adhesive. After immersion in the denture cleaners for a designated time, we evaluated the area of the sample plate still covered by denture adhesive. Cream adhesives were removed more completely after immersion in majority of the denture cleaners than in water. Powder adhesive was removed more quickly than cream adhesives. Cushion adhesive was not removed by immersion in either the denture cleaners or water control. Some denture cleaners could liquefy cream adhesives more than water, but these differences were not observed in case of powder and cushion adhesives. © 2015 John Wiley & Sons A/S and The Gerodontology Association. Published by John Wiley & Sons Ltd.

Selective Removal of Uranium from the Washing Solution of Uranium-Contaminated Soil

Energy Technology Data Exchange (ETDEWEB)

Kim, Seung Soo; Han, G. S.; Kim, G. N.; Koo, D. S.; Jeong, J. W.; Choi, J. W. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2015-10-15

This study examined selective removal methods of uranium from the waste solution by ion exchange resins or solvent extraction methods to reduce amount of the 2{sup nd} waste. Alamine-336, known as an excellent extraction reagent of uranium from the leaching solution of uranium ore, did not remove uranium from the acidic washing solution of soil. Uranyl ions in the acidic waste solution were sorbed on ampholyte resin with a high sorption efficiency, and desorbed from the resin by a washing with 0.5 M Na{sub 2}CO{sub 3} solution at 60 .deg. C. However, the uranium dissolved in the sulfuric acid solution was not sorbed onto the strong anion exchanger resins. A great amount of uranium-contaminated (U-contaminated) soil had been generated from the decommissioning of a uranium conversion plant. Our group has developed a decontamination process with washing and electrokinetic methods to decrease the amount of waste to be disposed of. However, this process generates a large amount of waste solution containing various metal ions.

IODINE REMOVAL EFFICIENCY IN NON-SUBMERGED AND SUBMERGED SELF-PRIMING VENTURI SCRUBBER

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MAJID ALI

2013-04-01

Full Text Available The objective of this conducted research is to study the iodine removal efficiency in a self-priming venturi scrubber for submerged and non-submerged operating conditions experimentally and theoretically. The alkaline solution is used as an absorbent, which is prepared by dissolving sodium hydroxide (NaOH and sodium thiosulphate (Na2S2O3 in water to remove the gaseous iodine (I2 from the gas. Iodine removal efficiency is examined at various gas flow rates and inlet concentrations of iodine for submerged and non-submerged operating conditions. In the non-submerged venturi scrubber, only the droplets take part in iodine removal efficiency. However, in a submerged venturi scrubber condition, the iodine gas is absorbed from gas to droplets inside the venturi scrubber and from bubbles to surrounding liquid at the outlet of a venturi scrubber. Experimentally, it is observed that the iodine removal efficiency is greater in the submerged venturi scrubber as compare to a non-submerged venturi scrubber condition. The highest iodine removal efficiency of 0.99±0.001 has been achieved in a submerged self-priming venturi scrubber condition. A mathematical correlation is used to predict the theoretical iodine removal efficiency in submerged and non-submerged conditions, and it is compared against the experimental results. The Wilkinson et al. correlation is used to predict the bubble diameter theoretically whereas the Nukiyama and Tanasawa correlation is used for droplet diameter. The mass transfer coefficient for the gas phase is calculated from the Steinberger and Treybal correlation. The calculated results for a submerged venturi scrubber agree well with experimental results but underpredicts in the case of the non-submerged venturi scrubber.

Iodine Removal Efficiency in Non-Submerged and Submerged Self-Priming Venturi Scrubber

Energy Technology Data Exchange (ETDEWEB)

Ali, Majid; Yan, Changqi; Sun, Zhongning; Gu, Haifeng; Wang, Junlong; Mehboob; Khurram [Harbin Engineering Univ., Harbin (China)

2013-04-15

The objective of this conducted research is to study the iodine removal efficiency in a self-priming venturi scrubber for submerged and non-submerged operating conditions experimentally and theoretically. The alkaline solution is used as an absorbent, which is prepared by dissolving sodium hydroxide (NaOH) and sodium thiosulphate (Na{sub 2}S{sub 2}O{sub 3}) in water to remove the gaseous iodine (I{sub 2}) from the gas. Iodine removal efficiency is examined at various gas flow rates and inlet concentrations of iodine for submerged and non-submerged operating conditions. In the non-submerged venturi scrubber, only the droplets take part in iodine removal efficiency. However, in a submerged venturi scrubber condition, the iodine gas is absorbed from gas to droplets inside the venturi scrubber and from bubbles to surrounding liquid at the outlet of a venturi scrubber. Experimentally, it is observed that the iodine removal efficiency is greater in the submerged venturi scrubber as compare to a non-submerged venturi scrubber condition. The highest iodine removal efficiency of 0.99±0.001 has been achieved in a submerged self-priming venturi scrubber condition. A mathematical correlation is used to predict the theoretical iodine removal efficiency in submerged and non-submerged conditions, and it is compared against the experimental results. The Wilkinson et al. correlation is used to predict the bubble diameter theoretically whereas the Nukiyama and Tanasawa correlation is used for droplet diameter. The mass transfer coefficient for the gas phase is calculated from the Steinberger and Treybal correlation. The calculated results for a submerged venturi scrubber agree well with experimental results but underpredicts in the case of the non-submerged venturi scrubber.

Iodine Removal Efficiency in Non-Submerged and Submerged Self-Priming Venturi Scrubber

International Nuclear Information System (INIS)

Ali, Majid; Yan, Changqi; Sun, Zhongning; Gu, Haifeng; Wang, Junlong; Mehboob; Khurram

2013-01-01

The objective of this conducted research is to study the iodine removal efficiency in a self-priming venturi scrubber for submerged and non-submerged operating conditions experimentally and theoretically. The alkaline solution is used as an absorbent, which is prepared by dissolving sodium hydroxide (NaOH) and sodium thiosulphate (Na 2 S 2 O 3 ) in water to remove the gaseous iodine (I 2 ) from the gas. Iodine removal efficiency is examined at various gas flow rates and inlet concentrations of iodine for submerged and non-submerged operating conditions. In the non-submerged venturi scrubber, only the droplets take part in iodine removal efficiency. However, in a submerged venturi scrubber condition, the iodine gas is absorbed from gas to droplets inside the venturi scrubber and from bubbles to surrounding liquid at the outlet of a venturi scrubber. Experimentally, it is observed that the iodine removal efficiency is greater in the submerged venturi scrubber as compare to a non-submerged venturi scrubber condition. The highest iodine removal efficiency of 0.99±0.001 has been achieved in a submerged self-priming venturi scrubber condition. A mathematical correlation is used to predict the theoretical iodine removal efficiency in submerged and non-submerged conditions, and it is compared against the experimental results. The Wilkinson et al. correlation is used to predict the bubble diameter theoretically whereas the Nukiyama and Tanasawa correlation is used for droplet diameter. The mass transfer coefficient for the gas phase is calculated from the Steinberger and Treybal correlation. The calculated results for a submerged venturi scrubber agree well with experimental results but underpredicts in the case of the non-submerged venturi scrubber

Studies on efficiency of guava (Psidium guajava) bark as bioadsorbent for removal of Hg (II) from aqueous solutions

Energy Technology Data Exchange (ETDEWEB)

Lohani, Minaxi B. [Integral University, Kursi Road, Lucknow 226026, UP (India)], E-mail: minaxi_lohani@sify.com; Singh, Amarika; Rupainwar, D.C. [Institute of Engineering and Technology Sitapur Road, Lucknow 226021, UP (India); Dhar, D.N. [IIT Kanpur (India)

2008-11-30

Biosorption of Hg (II) was investigated in this study by using guava bark powder (GBP). In the batch system, effects of various parameters like contact time, initial concentration, pH and temperature were investigated. Removal of Hg (II) was pH dependent and was found maximum at pH 9.0. Based on this study, the thermodynamic parameters like change in standard Gibb's free energy ({delta}G{sup 0}), standard enthalpy ({delta}H{sup 0}) and standard entropy ({delta}S{sup 0}) were evaluated. The rate kinetic study was found to follow second-order. The applicability of Freundlich adsorption isotherm model was tested. The value of regression coefficient was greater than 0.99. This indicated that the isotherm model adequately described the experimental data of the biosorption of Hg (II). Maximum adsorption of 3.364 mg g{sup -1} was reached at 80 min. The results of the study showed that guava bark powder can be efficiently used as a low-cost alternative for the removal of divalent mercury from aqueous solutions.

Studies on efficiency of guava (Psidium guajava) bark as bioadsorbent for removal of Hg (II) from aqueous solutions

International Nuclear Information System (INIS)

Lohani, Minaxi B.; Singh, Amarika; Rupainwar, D.C.; Dhar, D.N.

2008-01-01

Biosorption of Hg (II) was investigated in this study by using guava bark powder (GBP). In the batch system, effects of various parameters like contact time, initial concentration, pH and temperature were investigated. Removal of Hg (II) was pH dependent and was found maximum at pH 9.0. Based on this study, the thermodynamic parameters like change in standard Gibb's free energy (ΔG 0 ), standard enthalpy (ΔH 0 ) and standard entropy (ΔS 0 ) were evaluated. The rate kinetic study was found to follow second-order. The applicability of Freundlich adsorption isotherm model was tested. The value of regression coefficient was greater than 0.99. This indicated that the isotherm model adequately described the experimental data of the biosorption of Hg (II). Maximum adsorption of 3.364 mg g -1 was reached at 80 min. The results of the study showed that guava bark powder can be efficiently used as a low-cost alternative for the removal of divalent mercury from aqueous solutions

Removal of Uranium by Exchanger Resins from Soil Washing Solution

Energy Technology Data Exchange (ETDEWEB)

Kim, Seung Soo; Han, G. S.; Kim, G. N.; Koo, D. S.; Jeong, J. W.; Moon, J. K. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2015-05-15

Uranyl ions in the acidic waste solution were sorbed on AM-resin resin with a high sorption efficiency, and desorbed from the resin by a batch-type washing with a 60 .deg. C heated 0.5 M Na{sub 2}CO{sub 3} solution. However, the uranium dissolved in the sulfuric acid solution was not sorbed onto the strong anion exchanger resins. Our group has developed a decontamination process with washing and electrokinetic methods for uranium-contaminated (U-contaminated) soil. However, this process generates a large amount of waste solution containing various metal ions. If the uranium selectively removed from the waste solution, a very small amount of the 2nd waste would be generated. Thus, selective sorption of uranium by ion exchange resins was examined in this study.

Copper removal from aqueous solution using Aspergillus niger mycelia in free and polyurethane-bound form

Energy Technology Data Exchange (ETDEWEB)

Tsekova, K.; Ilieva, S. [Inst. of Microbiology, Bulgarian Academy of Sciences, Sofia (Bulgaria)

2001-07-01

This study assesses the ability of mycelia of Aspergillus niger B-77 (both free and immobilized on polyurethane foam) to remove copper from single-ion solution. All experiments were conducted using 0.5 mM solutions of CuSO{sub 4}.5H{sub 2} O. Mycelia immobilized on polyurethane foam cells showed a three-fold increase in uptake, compared with that of free cells. The efficiency of copper removal (mg Cu{sup 2+} removed/mg Cu{sup 2+} added) in a column system reached more than 99% before the break-through point was attained. (orig.)

Efficient removal of endosulfan from aqueous solution by UV-C/peroxides: A comparative study

Energy Technology Data Exchange (ETDEWEB)

Shah, Noor S. [Radiation Chemistry Laboratory, National Centre of Excellence in Physical Chemistry, University of Peshawar, Peshawar 25120 (Pakistan); Environmental Engineering and Science Program, University of Cincinnati, 705 Engineering Research Center, Cincinnati, OH 45221-0012 (United States); He, Xuexiang [Environmental Engineering and Science Program, University of Cincinnati, 705 Engineering Research Center, Cincinnati, OH 45221-0012 (United States); Khan, Hasan M. [Radiation Chemistry Laboratory, National Centre of Excellence in Physical Chemistry, University of Peshawar, Peshawar 25120 (Pakistan); Khan, Javed Ali [Radiation Chemistry Laboratory, National Centre of Excellence in Physical Chemistry, University of Peshawar, Peshawar 25120 (Pakistan); Environmental Engineering and Science Program, University of Cincinnati, 705 Engineering Research Center, Cincinnati, OH 45221-0012 (United States); O' Shea, Kevin E. [Department of Chemistry and Biochemistry, Florida International University, Miami, FL 33199 (United States); Boccelli, Dominic L. [Environmental Engineering and Science Program, University of Cincinnati, 705 Engineering Research Center, Cincinnati, OH 45221-0012 (United States); Dionysiou, Dionysios D., E-mail: dionysios.d.dionysiou@uc.edu [Environmental Engineering and Science Program, University of Cincinnati, 705 Engineering Research Center, Cincinnati, OH 45221-0012 (United States); Nireas-International Water Research Centre, University of Cyprus, 20537 Nicosia (Cyprus)

2013-12-15

Highlights: • Removal of endosulfan was studied by UV-C and UV-based advanced oxidation processes (AOPs). • Among UV/S{sub 2}O{sub 8}{sup 2−}, UV/HSO{sub 5}{sup −}, and UV/H{sub 2}O{sub 2}, endosulfan was removed the most efficiently by UV/S{sub 2}O{sub 8}{sup 2−}. • Hydroxyl and/or sulfate radicals were involved in the destruction of endosulfan and its by-products. • Presence of natural organic matter or alcohol inhibited the removal of endosulfan and its by-products. • Degradation pathways were proposed based on the nature of endosulfan degradation intermediates. -- Abstract: This study explored the efficiency of UV-C-based advanced oxidation processes (AOPs), i.e., UV/S{sub 2}O{sub 8}{sup 2−}, UV/HSO{sub 5}{sup −}, and UV/H{sub 2}O{sub 2} for the degradation of endosulfan, an organochlorine insecticide and an emerging water pollutant. A significant removal, 91%, 86%, and 64%, of endosulfan, at an initial concentration of 2.45 μM and UV fluence of 480 mJ/cm{sup 2}, was achieved by UV/S{sub 2}O{sub 8}{sup 2−}, UV/HSO{sub 5}{sup −}, and UV/H{sub 2}O{sub 2} processes, respectively, at a [peroxide]{sub 0}/[endosulfan]{sub 0} molar ratio of 20. The efficiency of these processes was, however, inhibited in the presence of radical scavengers, such as alcohols (e.g., tertiary butyl alcohol and isopropyl alcohol) and natural organic matter (NOM). The inhibition was also influenced by common inorganic anions in the order of nitrite > bicarbonate > chloride > nitrate ≃ sulfate. The observed pseudo-first-order rate constant decreased while the degradation rate increased with increasing initial concentration of the target contaminant. The degradation mechanism of endosulfan by the AOPs was evaluated revealing the main by-product as endosulfan ether. Results of this study suggest that UV-C-based AOPs are potential methods for the removal of pesticides, such as endosulfan and its by-products, from contaminated water.

Evaluation of Efficacy of Advanced Oxidation Processes Fenton, Fenton-like and Photo-Fenton for Removal of Phenol from Aqueous Solutions

International Nuclear Information System (INIS)

Mofrad, M. R.; Akbari, H.; Miranzadeh, M. B.; Nezhad, M. E.; Atharizade, M.

2015-01-01

Contamination of water, soil and groundwater caused by aromatic compounds induces great concern in most world areas. Among organic pollutants, phenol is mostly considered dangerous due to its high toxicity for human and animal. Advanced oxidation processes (AOPs) is considered as a most efficient method also the best one for purifying organic compounds which are resistant to conventional physical and chemical processes. This experimental study was carried out in laboratory scale. First, a synthetic solution was made of phenol. Then, Fenton, Fenton-like and photo-Fenton processes were applied removing phenol from aquatic solution. The effects of Hydrogen Peroxide concentration, catalyst, pH and time were studied to phenol removal efficiency. Results showed that Photo-Fenton process with removal efficiency (97.5 percentage) is more efficient than Fenton and Fenton-like processes with removal efficiency (78.7 percentage and 82.5 percentage respectively), in pH=3, (H/sub 2/O/sub 2/)= 3mM, (Fe2+)= 0.1 mM, phenol concentration 100 mg L-1 and time reaction 60 min, the phenol removal was 97.5 percentage. (author)

Efficient device for the benign removal of organic pollutants from aqueous solutions using modified mesoporous magnetite nanostructures

Science.gov (United States)

Vojoudi, H.; Badiei, A.; Amiri, A.; Banaei, A.; Ziarani, G. M.; Schenk-Joß, K.

2018-02-01

In this study, a home-made device comprising a column filled with magnetic mesoporous silica-coated nanostructures (MSCM-PA) as an adsorbent was constructed and used to remove organic pollutants from aqueous solutions. The MSCM-PA adsorbent was prepared and characterized using Fourier transform-infrared spectroscopy, ultraviolet-visible spectroscopy, scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, vibrating sample magnetometry, Brunauer-Emmett-Teller, thermogravimetric analysis/differential thermal analysis, and powder X-ray diffraction techniques. The adsorption behavior of the MSCM-PA sorbent was studied based on the removal of Everzol blue dye from aqueous solutions. We investigated the effects of various parameters such as the solution pH, initial dye concentration, adsorbent dose, flow rate, and contact time on the adsorption of Everzol blue from aqueous solutions. The adsorption data were modeled using Langmuir and Freundlich isotherms, and a good fit was obtained with the Langmuir isotherm. The maximum Everzol blue adsorption capacity by MSCM-PA was 162 mg g-1. The results indicate that our device is capable of adsorbing anionic dyes from aqueous solutions.

Removal of Cd 2+ ion from diluted aqueous solutions by electrodeposition on reticulated vitreous carbon electrodes

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Tramontina Jucelânia

2002-01-01

Full Text Available The electrodeposition of Cd2+ ion was investigated in pH 4.8 sulfuric-sulfate solutions in the presence of dissolved O2. In potentiostatic conditions, using reticulated vitreous carbon (RVC electrodes of 30, 60 and 100 pores per inch (ppi, high removal efficiency values were achieved in the potential range from --0.90 to --1.10 V for solutions containing 5 and 10 mg L-1 of Cd2+ ion. In this potential range, Cd electrodeposition is a mass transport controlled reaction and the concentration of the metallic ion decays exponentially with time following a pseudo-first order kinetics. For the 30 ppi RVC, the current efficiency and removal efficiency values found were, respectively, 45 % and 96 % for a solution containing 10 mg L-1 of Cd2+ ion after 30 minutes electrolysis at --0.90 V while 33 % and 99% were found for the 60 ppi RVC. The concentration decay of Cd2+ ion in the solution was monitored after each experiment by anodic stripping voltammetry at a hanging mercury drop electrode.

Removal of perfluoroalkyl sulfonates (PFAS) from aqueous solution using permanently confined micelle arrays (PCMAs)

KAUST Repository

Wang, Fei

2014-12-01

One new sorbent with permanently confined micelle arrays (PCMAs) has been synthesized to remove PFAS compounds from aquatic solutions. The TEM and SEM studies showed that large particle sizes with lots of macro-pores and highly order hexagonal structure of cylindrical micelle had been formed in the sorbent. The FTIR spectrums demonstrated the formation of Si-O-Si covalent bond in the new material. The kinetic study showed that the sorption of PFOS, PFHxS, and PFBuS by PCMAs reached equilibrium within 5 min. The pH and salts in solution are found to have limited effects on sorption of PFOS on the new sorbent, and regeneration experiments revealed that PFAS removal efficiencies by the PCMAs did not decrease after 5 cycle regenerations. The high capabilities of PCMAs make it a potentially attractive sorbent for the removal of PFCs from aqueous solution.

Study of the removal of metronidazole from aqueous solutions using Electro/ Fenton process and graphite and iron electrodes

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Bahram Kamarehie

2018-04-01

Conclusion: The Electro-Fenton process can effectively remove metronidazole from aquatic solutions in environmentally convenient conditions. This process can be used as an efficient method for removing other persistent pollutants from the environment.

Effect of garlic solution to Bacillus sp. removal

Science.gov (United States)

Zainol, N.; Rahim, S. R.

2018-04-01

Biofilm is a microbial derived sessile community characterized by cells that are irreversibly attached to a substratum or interface to each other, embedded in a matrix of extracellular polymeric substances that they have produced. Bacillus sp. was used as biofilm model in this study. The purpose of this study is to determine the effect of Garlic solution in term of ratio of water and Garlic solution (W/G) and ratio of Garlic solution to Bacillus sp. (GS/B) on Bacillus sp removal. Garlic solution was used to remove Bacillus sp. In this study, Garlic solution was prepared by crushing the garlic and mixed it with water. the Garlic solution was added into Bacillus sp. mixture and mixed well. The mixture then was spread on nutrient agar. The Bacillus sp. weight on agar plate was measured by using dry weight measurement method. In this study, initially Garlic solution volume and Garlic solution concentration were studied using one factor at time (OFAT). Later two-level-factorial analysis was done to determine the most contributing factor in Bacillus sp. removal. Design Expert software (Version 7) was used to construct experimental table where all the factors were randomized. Bacilus sp removal was ranging between 42.13% to 99.6%. The analysis of the results showed that at W/G of 1:1, Bacillus sp. removal increased when more Garlic solution was added to Bacillus sp. Effect of Garlic solution to Bacillus sp. will be understood which in turn may be beneficial for the industrial purpose.

Highly efficient removal of chlorotetracycline from aqueous solution using graphene oxide/TiO2 composite: Properties and mechanism

Science.gov (United States)

Li, Zhaoqian; Qi, Mengyu; Tu, Chunyan; Wang, Weiping; Chen, Jianrong; Wang, Ai-Jun

2017-12-01

The extensive usage of chlorotetracycline (CTC) has caused the persistence of antibiotic residues in aquatic environments, resulting in serious threat to human health and ecosystems. In this study, graphene oxide/titanium dioxide (GO/TiO2) nanocomposite was successfully synthesized via in situ hydrolysis of tetra-n-butyl titanate (Ti(BuO)4) to TiO2 particles on GO sheets and used as adsorbent for efficient adsorptive removal of CTC from aqueous solution. The prepared GO/TiO2 was characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transformed infrared (FT-IR), Raman spectroscopy and X-ray photoelectron (XPS). Adsorption kinetics, isotherms and thermodynamics were systematically investigated to evaluate the adsorption properties of GO/TiO2. Adsorption mechanism was further analyzed by FT-IR, UV-vis and XPS. The results indicated that adsorption kinetics closely followed the pseudo-second order model; the maximum adsorption capacity determined by Langmuir model was 261.10 mg g-1 at 298 K and the thermodynamic studies revealed that the adsorption of CTC onto the GO/TiO2 was a spontaneous and endothermic process. Moreover, the interactions between CTC and GO/TiO2 were presumed to be ligand exchange between CTC and TiO2, while the π-π electron donor-acceptor interaction, hydrogen bond and cation-π bonding were constructed between CTC and GO. Finally, the prepared GO/TiO2 was successfully applied for the efficient removal of CTC from Wu River water.

Simultaneous pollutant removal and electricity generation in denitrifying microbial fuel cell with boric acid-borate buffer solution.

Science.gov (United States)

Chen, Gang; Zhang, Shaohui; Li, Meng; Wei, Yan

2015-01-01

A double-chamber denitrifying microbial fuel cell (MFC), using boric acid-borate buffer solution as an alternative to phosphate buffer solution, was set up to investigate the influence of buffer solution concentration, temperature and external resistance on electricity generation and pollutant removal efficiency. The result revealed that the denitrifying MFC with boric acid-borate buffer solution was successfully started up in 51 days, with a stable cell voltage of 205.1 ± 1.96 mV at an external resistance of 50 Ω. Higher concentration of buffer solution favored nitrogen removal and electricity generation. The maximum power density of 8.27 W/m(3) net cathodic chamber was obtained at a buffer solution concentration of 100 mmol/L. An increase in temperature benefitted electricity generation and nitrogen removal. A suitable temperature for this denitrifying MFC was suggested to be 25 °C. Decreasing the external resistance favored nitrogen removal and organic matter consumption by exoelectrogens.

Process for the removal of radium from acidic solutions containing same

International Nuclear Information System (INIS)

Scheitlin, F.M.

1984-01-01

Radium is removed from an inorganic-acid solution contacting the solution with coal fly ash to effect adsorption of the radium on the ash. The radium-containing ash then is separated from the solution. The process is simple and efficient. High radium-distribution coefficients are obtained even at room temperature. Coal fly ash is an inexpensive, acid-resistant, high-surface-area material which is available in large quantities. The invention is applicable, for example, to the recovery of 226 Ra from nitric acid solutions which have been used to leach radium from uranium-mill tailings, and thus contain thorium and uranium. The contaminated fly ash may be incorporated in a suitable matrix and stored, and the residual solutions processed to separate uranium and thorium. (author)

Efficient removal of Cd2+ from aqueous solutions using by-product of biodiesel production

International Nuclear Information System (INIS)

Ribeiro, Rita F.L.; Soares, Vitor C.; Costa, Letícia M.; Nascentes, Clésia C.

2012-01-01

Highlights: ► Sorbents were prepared from radish cake, a waste from biodiesel production. ► The chemical treatments used were simple, low-cost and enhanced the Cd 2+ sorption. ► The cadmium sorption process was evaluated by Freundlich and Langmuir models. ► Chemically treated radish cake is an excellent alternative for removal of Cd 2+ . ► Desorption studies demonstrated that the sorbent–metal interaction is reversible. - Abstract: In this study, chemically modified radish cake, a by-product of biodiesel production, was used to remove Cd 2+ from aqueous solutions. The chemical modification was carried out by treating the radish cake with citric acid (CRC), NaOH (NRC) or the combination of citric acid and NaOH (CNRC). The sorbents were characterized by elemental analysis, surface area analysis, infrared spectroscopy (FTIR), potentiometric titration (PT), scanning electron microscopy–energy dispersive spectroscopy (SEM–EDS), and thermogravimetric analysis (TGA). The effect of the chemical treatment and contact time on cadmium sorption was evaluated. The equilibrium data were analyzed using Freundlich and Langmuir models. The maximum sorption capacity obtained by the Langmuir isotherm was 58.5 mg/g and 64.10 mg/g for the CRC, and CNRC sorbents, respectively. Complete desorption of Cd 2+ was achieved using 0.1 mol/L HNO 3 . The results obtained demonstrate that chemically modified radish cake has potential as a sorbent for Cd 2+ removal from aqueous solutions.

Nitrate Removal from Aqueous Solutions Using Almond Charcoal Activated with Zinc Chloride

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Mohsen Arbabi

2017-10-01

Full Text Available Background & Aims of the Study: Nitrate is one of the most important contaminants in aquatic environments that can leached to water resources from various sources such as sewage, fertilizers and decomposition of organic waste. Reduction of nitrate to nitrite in infant’s blood stream can cause “blue baby” disease in infants. The aim of this study was to evaluate the nitrate removal from aqueous solutions using modified almond charcoal with zinc chloride. Materials &Methods: This study is an experimental survey. At the first charcoal almond skins were prepared in 5500C and then modified with ZnCl2. Morphologies and characterization of almond shell charcoal were evaluated by using FTIR, EDX, BET and FESEM. Adsorption experiments were conducted with 500 ml sample in Becker. The nitrate concentration removal, contact time, pH and charcoal dosage were investigated. The central composite design method was used to optimizing the nitrate removal process. The results analyzed with ANOVA test. Results: The best condition founded in 48 min, 1250 ppm, 125 mg/l and 3 for retention time, primary nitrate concentration, charcoal dosage and pH respectively. The results showed that the nitrate removal decreases with increasing pH. Modification of skin charcoal is show increasing of nitrate removal from aquatic solution. Conclusion: In this study, the maximum nitrate removal efficiency for raw charcoal and modified charcoal was determined 15.47% and 62.78%, respectively. The results showed that this method can be used as an effective method for removing nitrate from aqueous solutions.

Nanotoxicity modelling and removal efficiencies of ZnONP.

Science.gov (United States)

Fikirdeşici Ergen, Şeyda; Üçüncü Tunca, Esra

2018-01-02

In this paper the aim is to investigate the toxic effect of zinc oxide nanoparticles (ZnONPs) and is to analyze the removal of ZnONP in aqueous medium by the consortium consisted of Daphnia magna and Lemna minor. Three separate test groups are formed: L. minor ([Formula: see text]), D. magna ([Formula: see text]), and L. minor + D. magna ([Formula: see text]) and all these test groups are exposed to three different nanoparticle concentrations ([Formula: see text]). Time-dependent, concentration-dependent, and group-dependent removal efficiencies are statistically compared by non-parametric Mann-Whitney U test and statistically significant differences are observed. The optimum removal values are observed at the highest concentration [Formula: see text] for [Formula: see text], [Formula: see text] for [Formula: see text]and [Formula: see text] for [Formula: see text] and realized at [Formula: see text] for all test groups [Formula: see text]. There is no statistically significant differences in removal at low concentrations [Formula: see text] in terms of groups but [Formula: see text] test groups are more efficient than [Formula: see text] test groups in removal of ZnONP, at [Formula: see text] concentration. Regression analysis is also performed for all prediction models. Different models are tested and it is seen that cubic models show the highest predicted values (R 2 ). In toxicity models, R 2 values are obtained at (0.892, 0.997) interval. A simple solution-phase method is used to synthesize ZnO nanoparticles. Dynamic Light Scattering and X-Ray Diffraction (XRD) are used to detect the particle size of synthesized ZnO nanoparticles.

Investigation of Phenol Removal from Aqueous Solutions by Electrofenton and Electropersulfate Processes

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Alireza Rahmani

2016-11-01

Full Text Available Phenol, or benzene hydroxyl is a toxic aromatic hydrocarbon discharged into the environment through certian industrial effluents which, thereby, pollute water resources. This study examines phenol removal from aqueous solutions through electro-Fenton and electro/persulfate processes using iron electrodes. For this purpose, a laboratory-scale electrochemical batch reactor was used that was equipped with four electrodes and a direct DC power supply. In the tests carried out, the effects of operational parameters such as initial pH; current density; and initial concentrations of phenol, hydrogen peroxide, and persulfate on the removal of phenol were investigated. The results showed that EPS and EF processes achieved phenol removal efficiencies of 95.18% and 93.99%, respectively, at operating conditions of pH = 3, initial phenol concentration of 100 mg/l, hydrogen peroxide and persulfate concentration of 0. 4 mM, and a current density 0.07A/dm2 over 45 min. Increasing persulfate and hydrogen peroxide concentration from 0.4 to 0.8 mM reduced phenol removal efficiencies from 95.18% and 93.99% to 43% and 85%, respectively. Generally speaking, EPS and EF processes exhibited almost identical phenol removal efficiencies. Finally, the integrated electrochemical and persulphate process was found to be more productive in producing electrical iron and persulphate activation than using each single process in isolation.

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

International Nuclear Information System (INIS)

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

2014-01-01

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

Mercury nano-trap for effective and efficient removal of mercury(II) from aqueous solution

Science.gov (United States)

Li, Baiyan; Zhang, Yiming; Ma, Dingxuan; Shi, Zhan; Ma, Shengqian

2014-11-01

Highly effective and highly efficient decontamination of mercury from aqueous media remains a serious task for public health and ecosystem protection. Here we report that this task can be addressed by creating a mercury ‘nano-trap’ as illustrated by functionalizing a high surface area and robust porous organic polymer with a high density of strong mercury chelating groups. The resultant porous organic polymer-based mercury ‘nano-trap’ exhibits a record-high saturation mercury uptake capacity of over 1,000 mg g-1, and can effectively reduce the mercury(II) concentration from 10 p.p.m. to the extremely low level of smaller than 0.4 p.p.b. well below the acceptable limits in drinking water standards (2 p.p.b.), and can also efficiently remove >99.9% mercury(II) within a few minutes. Our work therefore presents a new benchmark for mercury adsorbent materials and provides a new perspective for removing mercury(II) and also other heavy metal ions from contaminated water for environmental remediation.

FACTORS AFFECTING THE REMOVAL OF A BASIC AND AN AZO DYE FROM ARTIFICIAL SOLUTIONS BY ADSORPTION USING ACTIVATED CARBON

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H Albroomi

2014-10-01

Full Text Available Decolourisation of wastewater, particularly from textile industries, is one of the major environmental concerns these days. Current methods for removing dyes from wastewater are costly and cannot effectively be used to treat wide range of such wastewater. This work describes the use of commercial available granular activated carbon (GAC as an efficient adsorbent material for dyes removal. Aqueous solutions of various basic dye Methylene Blue (MB and azo-dye Tartrazine with concentrations 5-20 mg l–1 and 10-100 mg l–1, respectively, were shaken with certain amount of GAC to determine the adsorption capacity and removal efficiencies. The effects of adsorbent dose, initial pH, initial dye concentration, agitation speed and contact time on dyes removal efficiencies have been studied. Maximum dye concentration was removed from the solution within 60-90 min after the beginning of every experiment. Adsorption parameters were found to fit well into Langmuir and Freundlich adsorption isotherms models with correlation coefficient (R2 > 0.99 in the concentration range of MB and TZ studied.

Removal of phenol from aqueous solution using polymer inclusion membrane based on mixture of CTA and CA

Science.gov (United States)

Benosmane, Nadjib; Boutemeur, Baya; Hamdi, Safouane M.; Hamdi, Maamar

2018-03-01

Nowadays, there are increasingly stringent regulations requiring more and more treatment of industrial effluents to generate product waters which could be easily reused or disposed of to the environment without any harmful effects. In the present work, the removal of phenol from aqueous solution across polymer inclusion membrane (PIM), based on mixture of cellulose triacetate and cellulose acetate as support (75/25%), calix[4]resorcinarene derivative as a carrier and 2-nitrophenyl octyl ether (2-NPOE) as plasticizer was investigated. The experimental part of this investigation involved the influence of carrier nature, plasticizer concentration, pH phases, and phenol initial concentration on the removal efficiency of phenol from synthetic wastewater. A PIM containing 0.1 g (of mixture polymer), (0.15 g/g mixture of polymer) of carrier and (0.03 ml/g mixture of polymer) of 2-NPOE provided the highest percentage of phenol removal efficiency over a 6-day transport; the removal was found to be about 95%, indeed the removal was found to be highly dependent of pH phases. The feed solution in these transport experiments was at pH 2, while the stripping solution contained 0.20 M NaOH. This study claims that the PIM with a mixture of cellulose derivatives can be used effectively to remove phenols from wastewaters.

Removal of cadmium from aqueous solution using marine green algae, Ulva lactuca

Directory of Open Access Journals (Sweden)

Mohamed M. Ghoneim

2014-01-01

Full Text Available The present study aimed to evaluate the efficiency of marine algae for removal of metals from the aqueous solution. The green alga, Ulva lactuca, collected from the intertidal zone of the Suez Bay, northern part of the Red Sea was used to reduce cadmium levels from the aqueous solutions. The biosorption mechanisms of Cd2+ ions onto the algal tissues were examined using various analytical techniques: Fourier-transform infrared spectroscopy (FT-IR and Scanning electron microscopy (SEM. Results indicated that at the optimum pH value of 5.5; about 0.1 g of U. lactuca was enough to remove 99.2% of 10 mg L−1 Cd2+ at 30 °C in the aqueous solutions. The equilibrium data were well fitted with the Langmuir and Freundlich isotherms. The monolayer adsorption capacity was 29.1 mg g−1. The calculated RL and ‘n’ values have proved the favorability of cadmium adsorption onto U. lactuca. The desorption test revealed that HCl was the best for the elution of metals from the tested alga. In conclusion, the seaweed U. lactuca was the favorable alternative of cadmium removal from water.

Selective removal of mercury from aqueous solutions using thiolated cross-linked polyethylenimine

Science.gov (United States)

Saad, Dalia M.; Cukrowska, Ewa M.; Tutu, Hlanganani

2013-06-01

A successful approach to develop an insoluble form of polyethylenimine with a thiol-based functional group for selective removal of Hg(II) from aqueous solutions is reported. The selectivity of the modified polymer for Hg(II) as well as its ability to be regenerated for re-use has been studied. The synthesised polymer exhibited high selectivity for Hg(II) with high removal efficiency of up to 97 %, even in the presence of competing ions. The Freundlich isotherm was found to best fit and describe the experimental data. The pseudo-second-order equation explains the adsorption kinetics most effectively implying chemisorption. The thermodynamic study of the adsorption process revealed high activation energies >41 kJ mol-1, further confirming chemisorption as the mechanism of interaction between mercury ions and the polymer surface. The polymer exhibited good potential for re-use after many cycles of regeneration, giving good removal efficiency up to the fifth cycle.

Efficiency of water removal from water/ethanol mixtures using supercritical carbon dioxide

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M. A. Rodrigues

2006-06-01

Full Text Available Techniques involving supercritical carbon dioxide have been successfully used for the formation of drug particles with controlled size distributions. However, these processes show some limitations, particularly in processing aqueous solutions. A diagram walking algorithm based on available experimental data was developed to evaluate the effect of ethanol on the efficiency of water removal processes under different process conditions. Ethanol feeding was the key parameter resulting in a tenfold increase in the efficiency of water extraction.

Novel geochemistry-inspired method for the deep removal of vanadium from molybdate solution

Energy Technology Data Exchange (ETDEWEB)

Zhang, Jialiang [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing, 100083 (China); Beijing Key Laboratory of Green Recycling and Extraction of Metals, Beijing, 100083 (China); Deng, Yuping; Zhou, Qiuyue; Qin, Peixin; Liu, Yubo [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing, 100083 (China); Wang, Chengyan, E-mail: chywang@yeah.net [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing, 100083 (China)

2017-06-05

Highlights: • A geochemistry-inspired method was developed for removal of V from molybdates. • Magnetic separation of the Fe{sub 3}O{sub 4} adsorbent took 10 s. • Vanadium can be deeply removed in 5 min at pH of 7.0–11.0. • Fe{sub 3}O{sub 4} adsorbent has excellent V selectivity and reusability. • A flowchart is presented for Mo/V separation in the leachate of spent HDS catalyst. - Abstract: Separation of vanadium from molybdates is an essential task for processing the leaching solution of hazardous spent hydrodesulphurization (HDS) catalyst. In this study, the difference in the main naturally occurring mineral forms of Mo and V inspired us to develop a method for the deep removal of V from molybdate solution using Fe{sub 3}O{sub 4} as an adsorbent. First, the adsorbent was synthesized with coprecipitation method, and then it was characterized by XRD, TEM, and VSM. The synthesized material consisted of pure Fe{sub 3}O{sub 4} nanoparticles that exhibited paramagnetic property, with a saturated magnetization of 68.6 emu g{sup −1}. The V removal efficiency was investigated using batch adsorption experiments in varying conditions. Results indicated that V could be deeply removed from various concentrations of molybdate solution at pH of 7.0–11.0 within 5 min. A slight decrease was found in the adsorption ratio after the adsorbent had been reused for 4 cycles. The resulting molybdate solution contained less than 0.02 g L{sup −1} of V, which satisfies the requirement for preparing high-quality products. Finally, a process flowchart is presented for the separation of Mo and V from the leaching solution of spent HDS catalyst, based on the excellent V removal performance and rapid separation rate of the Fe{sub 3}O{sub 4} adsorbent.

A Ti-doped γ-Fe2O3/SDS nano-photocatalyst as an efficient adsorbent for removal of methylene blue from aqueous solutions.

Science.gov (United States)

Mirbagheri, Naghmeh Sadat; Sabbaghi, Samad

2018-05-01

Synthetic dyes are among the most important environmental pollutants in wastewaters. Consequently, elimination of the synthetic dyes from wastewaters using non-toxic materials and eco-friendly technologies has been of considerable interests. In this study, magnetically separable Ti-doped γ-Fe 2 O 3 photocatalysts were synthesized for the removal of methylene blue (MB) from a dye-contaminated aqueous solution (as a model of dye-polluted wastewaters). Compared to the pristine γ-Fe 2 O 3 , the 1.78 v% Ti-doped γ-Fe 2 O 3 significantly increased the adsorption of MB by 57% in the dark condition as a result of the improved BET surface area in this photocatalyst. Moreover, the contact time required for the photocatalytic degradation of MB by the 1.78 v% Ti-doped γ-Fe 2 O 3 decreased due to the higher concentration of charge carriers in this photocatalyst than that of the pristine γ-Fe 2 O 3 . The effect of different experimental parameters on the adsorption property and photocatalytic activity of the 1.78 v% Ti-doped γ-Fe 2 O 3 photocatalyst showed that the solution pH had a remarkable influence on the removal performance of this photocatalyst. Surface treatment of the 1.78 v% Ti-doped γ-Fe 2 O 3 with sodium dodecyl sulfate (SDS) resulted in the formation of a negatively charged Ti-doped γ-Fe 2 O 3 /SDS photocatalyst, which showed a higher tendency for the adsorption and removal of MB than the untreated photocatalyst. Moreover, the MB removal efficiency of this photocatalyst was among the best performances that have been reported for the γ-Fe 2 O 3 -based photocatalysts. The synthesized photocatalysts were characterized by various techniques, and a plausible mechanism for the removal of MB from aqueous solutions by the Ti-doped γ-Fe 2 O 3 /SDS photocatalyst was purposed. Copyright © 2018 Elsevier Ltd. All rights reserved.

Removal of perfluoroalkyl sulfonates (PFAS) from aqueous solution using permanently confined micelle arrays (PCMAs)

KAUST Repository

Wang, Fei; Lu, Xingwen; Shih, Kaimin; Wang, Peng; Li, Xiaoyan

2014-01-01

within 5 min. The pH and salts in solution are found to have limited effects on sorption of PFOS on the new sorbent, and regeneration experiments revealed that PFAS removal efficiencies by the PCMAs did not decrease after 5 cycle regenerations. The high

Efficiency of Chitosan for the Removal of Pb (II, Fe (II and Cu (II Ions from Aqueous Solutions

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Soheil Sobhanardakani

2014-09-01

Full Text Available Background: Heavy metals have been recognized as harmful environmental pollutant known to produce highly toxic effects on different organs and systems of both humans and animals. The aim of this paper is to evaluate the adsorption potential of chitosan for the removal of Pb(II, Fe(II and Cu(II ions from aqueous solutions. Methods: This study was conducted in laboratory scale. In this paper chitosan has been used as an adsorbent for the removal of Pb(II, Fe(II and Cu(II from aqueous solution. In batch tests, the effects of parameters like pH solution (1.0-8.0, initial metal concentrations (100-1000 mgL-1, contact time (5.0-150 min and adsorbent dose (1.0-7.0 g on the adsorption process were studied. Results: The results showed that the adsorption of Pb(II, Fe(II and Cu(II ions on chitosan strongly depends on pH. The experimental isothermal data were analyzed using the Langmuir and Freundlich equations and it was found that the removal process followed the Langmuir isotherm and maximum adsorption capacity for the adsorption of Pb(II, Fe(II and Cu(II ions by the chitosan were 55.5mg g−1, 71.4 mg g−1 and 59 mg g−1, respectively, under equilibrium conditions at 25±1 ºC. The adsorption process was found to be well described by the pseudo-second-order rate model. Conclusion: The obtained results showed that chitosan is a readily, available, economic adsorbent and was found suitable for removing Pb(II, Fe(II and Cu(II ions from aqueous solution.

Application of Azolla for 2-Chlorophenol and 4-Chrorophenol Removal from Aqueous Solutions

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Mohammad Ali Zazouli

2013-09-01

Full Text Available Background and purpose: The 2-chlorophenol (2-CP and 4-chlorophenol (4-CP are phenolic compounds which may have adverse effects on human and environment. Therefore, removing these compounds from water and wastewater is necessary. This study aims to analyze 2-CP and 4-CP removal by using Azolla filiculoides biomass. Materials & Methods: Azolla biomass was sun dried, crushed and sieved to particle sizes ranging 1-2 mm. Then it was treated with 0.1M HCl for 5h followed by washing with distilled water and it was used as adsorbent. The residues concentration of 2-CP and 4-CP was measured by spectrophotometer in λmax of 274 and 280 nm, respectively. Results: The solute removed increases as contact time rises. The equilibrium time for 2-CP and 4-CP is 90 and 75, respectively. The removal efficiency of 4-CP is more than 2-CP. An increase in initial concentration of both compounds can lead to decrease of their removal efficiency. The optimum pH to remove both compounds is 5. The equilibrium data matched best on Freundlich isotherm and the adsorption kinetic model follows pseudo-second model. Conclusion: The results indicated that Azolla is an effective adsorbent for removing 2-CP and 4-CP from water and wastewater.

Arsenic removal in solution using non living bio masses of aquatic weed

International Nuclear Information System (INIS)

Marin A, M. J.

2010-01-01

Arsenic is a metalloid considered among the most dangerous to health. The As maximum level allowed of drinkable water is 0.01 mg/L established by the Who. Several techniques have been proposed to remove arsenic from water, among which are the sorption processes in economic biological materials, which has advantages for its high efficiency in dilute toxic removing from contaminated water, for these reason it is necessary to study new bio sorbents materials which are economic, simple and easy to apply in the treatment of contaminated areas. The aim of this project was evaluate the removal of As (V) in solution using two non living aquatic plants: water hyacinth (Eichhornia crassipes) and lesser duckweed (Lemna minor), characterize these materials and compare the efficiency between both; the parameters evaluated were the As (V) initial concentration in solution, contact time, ph value and the amount of biomass in contact with them. It describes the method to prepare the non living plants. The physicochemical characterization by scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis was made. The results shown that cellulose is the main component confirmed by the techniques above mentioned. Surface characterization of Eichhornia crassipes and Lemna minor by specific surface area, shown 1.3521 m 2 /g and 0.6395 m 2 /g respectively, the hydration kinetic indicates that 24 h was the maximum hydration time for both plants; the point of zero charge determination by mass titration gives a ph=6.1 for the first plant and ph=7.1 for the second plant, finally the active site density obtained for the plants were of 8.57 sites/nm 2 and 12.47 sites/nm 2 . The point of zero charge was analyzed for know the ph from which the As (V) species are removal preferably. Tested contact processes between bio sorbent-As (V) were performed to assess the ability of bio masses to removal As (V) from aqueous solutions, investigated

Removal of Congo red dye from aqueous solutions using a halloysite-magnetite-based composite.

Science.gov (United States)

Ferrarini, F; Bonetto, L R; Crespo, Janaina S; Giovanela, M

2016-01-01

Adsorption has been considered as one of the most effective methods to remove dyes from aqueous solutions due to its ease of operation, high efficiency and wide adaptability. In view of all these aspects, this study aimed to evaluate the adsorption capacity of a halloysite-magnetite-based composite in the removal of Congo red dye from aqueous solutions. The effects of stirring rate, pH, initial dye concentration and contact time were investigated. The results revealed that the adsorption kinetics followed the pseudo-second-order model, and equilibrium was well represented by the Brunauer-Emmett-Teller isotherm. The thermodynamic data showed that dye adsorption onto the composite was spontaneous and endothermic and occurred by physisorption. Finally, the composite could also be regenerated at least four times by calcination and was shown to be a promising adsorbent for the removal of this dye.

Optimization of uranyl ions removal from aqueous solution by natural and modified kaolinites

Energy Technology Data Exchange (ETDEWEB)

Elhefnawy, O.A.; Elabd, A.A. [Nuclear and Radiological Regulatory Authority (NRRA), Cairo (Egypt). Nuclear Safeguards and Physical Protection Dept.

2017-10-01

The paper addresses the modifications of the most common mineral clay ''kaolinite'' for U(VI) removal from aqueous solutions. A new modified Egyptian natural kaolinite (Ca-MK) was prepared by coating kaolinite with calcium oxide. Another modification process was utilized by calcination and acid activation of kaolinite (E-MK). The Egyptian natural kaolinite (E-NK) and the two modified kaolinites were characterized by different techniques SEM, EDX, XRD, and FTIR. The removal process were investigated in batch experiments as a function of pH, contact time, initial U(VI) concentration, effect of temperature, and recovery of U(VI) were studied. The equilibrium stage was achieved after 60 min and the kinetic data was described well by pseudo-second order model. Isothermal data was better described by the Langmuir isotherm model, indicating the homogeneous removal process. Also the removal process was studied on different temperature 293, 313, and 323 K. The thermodynamic parameters ΔH , ΔS , and ΔG were calculated. The thermodynamic results pointed to the endothermic and favorable nature of the U(VI) removal process in the three kaolinite adsorbents. This study indicated that (Ca-MK) has higher CEC and can be used as a new adsorbent for highly efficient removal of U(VI) from aqueous solutions.

Virus removal efficiency of Cambodian ceramic pot water purifiers.

Science.gov (United States)

Salsali, Hamidreza; McBean, Edward; Brunsting, Joseph

2011-06-01

Virus removal efficiency is described for three types of silver-impregnated, ceramic water filters (CWFs) produced in Cambodia. The tests were completed using freshly scrubbed filters and de-ionized (DI) water as an evaluation of the removal efficiency of the virus in isolation with no other interacting water quality variables. Removal efficiencies between 0.21 and 0.45 log are evidenced, which is significantly lower than results obtained in testing of similar filters by other investigators utilizing surface or rain water and a less frequent cleaning regime. Other experiments generally found virus removal efficiencies greater than 1.0 log. This difference may be because of the association of viruses with suspended solids, and subsequent removal of these solids during filtration. Variability in virus removal efficiencies between pots of the same manufacturer, and observed flow rates outside the manufacturer's specifications, suggest tighter quality control and consistency may be needed during production.

Fixed-bed column study for 90Sr removal from solution by sunflower straw

International Nuclear Information System (INIS)

Ai Lian; Luo Xuegang; Lin Xiaoyan; Li Wenming

2014-01-01

This paper deals with removal of strontium ions from solution by sunflower straw. Metal sorption performance of the packed column was assessed under variable operating conditions, such as, bed depths, flow rates and initial influent strontium concentration. It was found that the breakthrough time and the depletion time were extended with increase of bed heights but obviously shortened with increase of influent concentration and flow rates, respectively. The equilibrium uptake (q e(exp) ) of sunflower straw increased with increase in initial influent strontium concentration and flow rates but decreased with increase in bed depth, respectively. The data in regard to the effect of bed depths were fitted well to the Bohrat-Adams model. The saturated column was successfully regenerated by 0.1 mol/L hydrogen chloride solution and sunflower straw could be reused in strontium removal. The results indicated that the column could efficiently remove strontium ions from real industrial effluents, and hence the sunflower straw is a good candidate for commercial application. (authors)

Electrocoagulation-Adsorption to Remove Anionic and Cationic Dyes from Aqueous Solution by PV-Energy

Directory of Open Access Journals (Sweden)

J. Castañeda-Díaz

2017-01-01

Full Text Available The cationic dye malachite green (MG and the anionic dye Remazol yellow (RY were removed from aqueous solutions using electrocoagulation-adsorption processes. Batch and continuous electrocoagulation procedures were performed and compared. Carbonaceous materials obtained from industrial sewage sludge and commercial activated carbons were used to adsorb dyes from aqueous solutions in column systems with a 96–98% removal efficiency. The continuous electrocoagulation-adsorption system was more efficient for removing dyes than electrocoagulation alone. The thermodynamic parameters suggested the feasibility of the process and indicated that the adsorption was spontaneous and endothermic (ΔS=0.037 and −0.009 for MG and RY, resp.. The ΔG value further indicated that the adsorption process was spontaneous (−6.31 and −10.48; T=303 K. The kinetic electrocoagulation results and fixed-bed adsorption results were adequately described using a first-order model and a Bohart-Adams model, respectively. The adsorption capacities of the batch and column studies differed for each dye, and both adsorbent materials showed a high affinity for the cationic dye. Thus, the results presented in this work indicate that a continuous electrocoagulation-adsorption system can effectively remove this type of pollutant from water. The morphology and elements present in the sludge and adsorbents before and after dye adsorption were characterized using SEM-EDS and FT-IR.

Electrochemical removal of copper ions from dilute solutions using packed bed electrode. Part І

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I.A. Khattab

2013-06-01

Full Text Available Removal of some hazardous waste like copper from effluent streams has an industrial importance. In this field, this paper is directed towards electrochemical removal of copper ions from sulfate solution using packed bed electrode. The cathode packing is in static mode, consisted of graphite particles, with mean particle size equal to 0.125 cm. The high surface area of this cell is expected to give high current efficiency and removal percent. The effect of current density and liquid flow rate were tested. Experimental results obtained indicate that the efficiencies are in direct proportional with current density while inversely proportional with liquid flow rate. It was observed that, using this cell was effective in reducing copper concentration to less than 4 mg/l with R.E of 96.2% during 30 min electrolysis time.

Application of H2O2 and H2O2/Fe0 in removal of Acid Red 18 dye from aqueous solutions

Directory of Open Access Journals (Sweden)

Nazari Shahram

2013-08-01

Full Text Available Background & Aims of the Study: Organic dyes with a complex structure are often toxic, carcinogenic, mutagenic, non-biodegradation and stable in the environment and if released to the environment without treatment can endanger the environment and human health. The aim of this study was to evaluate the performance of H2O2 and H2O2/Fe0 Iron in removal of dye Acid Red 18 from aqueous solutions. Materials & Methods: This study was conducted at the laboratory scale. In this study, the removal efficiency of Acid Red 18 from a synthetic solution by H2O2 and H2O2/Fe0 was investigated. As well as Effect of solution pH, dye concentration, Concentration of Nanoscale Zero-Valent Iron, H2O2 and contact time in decolorization efficiency was investigated. Results: Results show that in pH=3, Contact time of 80 minutes, dye concentration of 50 mg/l and Concentration of Nanoscale Zero-Valent Iron of 2 g/l and H2O2 concentration equal to 200 mmol/l, the removal efficiency was about 98%. Conclusions: According to the results of experiments, H2O2/Fe0 has high efficiency in removal of Acid Red 18 from aqueous solution.

Efficient removal of Cd{sup 2+} from aqueous solutions using by-product of biodiesel production

Energy Technology Data Exchange (ETDEWEB)

Ribeiro, Rita F.L., E-mail: ritaflavia@gmail.com [Departamento de Quimica, Instituto de Ciencias Exatas, Universidade Federal de Minas Gerais, Belo Horizonte, MG (Brazil); Soares, Vitor C., E-mail: vcelios@gmail.com [Departamento de Quimica, Instituto de Ciencias Exatas, Universidade Federal de Minas Gerais, Belo Horizonte, MG (Brazil); Costa, Leticia M., E-mail: leticia@qui.ufmg.br [Departamento de Quimica, Instituto de Ciencias Exatas, Universidade Federal de Minas Gerais, Belo Horizonte, MG (Brazil); Nascentes, Clesia C., E-mail: clesia@qui.ufmg.br [Departamento de Quimica, Instituto de Ciencias Exatas, Universidade Federal de Minas Gerais, Belo Horizonte, MG (Brazil)

2012-10-30

Highlights: Black-Right-Pointing-Pointer Sorbents were prepared from radish cake, a waste from biodiesel production. Black-Right-Pointing-Pointer The chemical treatments used were simple, low-cost and enhanced the Cd{sup 2+} sorption. Black-Right-Pointing-Pointer The cadmium sorption process was evaluated by Freundlich and Langmuir models. Black-Right-Pointing-Pointer Chemically treated radish cake is an excellent alternative for removal of Cd{sup 2+}. Black-Right-Pointing-Pointer Desorption studies demonstrated that the sorbent-metal interaction is reversible. - Abstract: In this study, chemically modified radish cake, a by-product of biodiesel production, was used to remove Cd{sup 2+} from aqueous solutions. The chemical modification was carried out by treating the radish cake with citric acid (CRC), NaOH (NRC) or the combination of citric acid and NaOH (CNRC). The sorbents were characterized by elemental analysis, surface area analysis, infrared spectroscopy (FTIR), potentiometric titration (PT), scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS), and thermogravimetric analysis (TGA). The effect of the chemical treatment and contact time on cadmium sorption was evaluated. The equilibrium data were analyzed using Freundlich and Langmuir models. The maximum sorption capacity obtained by the Langmuir isotherm was 58.5 mg/g and 64.10 mg/g for the CRC, and CNRC sorbents, respectively. Complete desorption of Cd{sup 2+} was achieved using 0.1 mol/L HNO{sub 3}. The results obtained demonstrate that chemically modified radish cake has potential as a sorbent for Cd{sup 2+} removal from aqueous solutions.

Efficient removal of tetracycline with KOH-activated graphene from aqueous solution.

Science.gov (United States)

Ma, Jie; Sun, Yiran; Yu, Fei

2017-11-01

Activated graphene absorbents with high specific surface area (SSA) were prepared by an easy KOH-activated method, and were applied in absorbing antibiotics, such as tetracycline (TC). After activation, many micropores were introduced to graphene oxide sheets, leading to higher SSA and many new oxygen-containing functional groups, which gave KOH-activated graphene excellent adsorption capacity (approx. 532.59 mg g -1 ) of TC. Further study on the adsorption mechanism showed that the Langmuir isotherm model and the pseudo-second-order kinetic model fitted with experiment data. To further understand the adsorption process, the effects of solid-liquid ratio, pH, ionic strength and coexisting ions were also investigated. The results revealed that, compared with pH and ionic strength, solid-liquid ratio and coexisting ions (Cu 2+ , CrO 4 2- ) had more significant influence over the adsorption performance. The findings provide guidance for application of KOH-activated graphene as a promising alternative adsorbent for antibiotics removal from aqueous solutions.

Heating Changes Bio-Schwertmannite Microstructure and Arsenic(III Removal Efficiency

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Xingxing Qiao

2017-01-01

Full Text Available Schwertmannite (Sch is an efficient adsorbent for arsenic(III removal from arsenic(III-contaminated groundwater. In this study, bio-schertmannite was synthesized in the presence of dissolved ferrous ions and Acidithiobacillus ferrooxidans LX5 in a culture media. Bio-synthesized Sch characteristics, such as total organic carbon (TOC, morphology, chemical functional groups, mineral phase, specific surface area, and pore volume were systematically studied after it was dried at 105 °C and then heated at 250–550 °C. Differences in arsenic(III removal efficiency between 105 °C dried-sch and 250–550 °C heated-sch also were investigated. The results showed that total organic carbon content in Sch and Sch weight gradually decreased when temperature increased from 105 °C to 350 °C. Sch partly transformed to another nanocrystalline or amorphous phase above 350 °C. The specific surface area of 250 °C heated-sch was 110.06 m2/g compared to 5.14 m2/g for the 105 °C dried-sch. Total pore volume of 105 °C dried-sch was 0.025 cm3/g with 32.0% mesopore and 68.0% macropore. However, total pore volume of 250 °C heated-mineral was 0.106 cm3/g with 23.6% micropore, 33.0% mesopore, and 43.4% macropore. The arsenic(III removal efficiency from an initial 1 mg/L arsenic(III solution (pH 7.5 was 25.1% when 0.25 g/L of 105 °C dried-sch was used as adsorbent. However, this efficiency increased to 93.0% when using 250 °C heated-sch as adsorbent. Finally, the highest efficiency for arsenic(III removal was obtained with sch-250 °C due to high amounts of sorption sites in agreement with the high specific surface area (SSA obtained for this sample.

MODELING AN ION EXCHANGE PROCESS FOR CESIUM REMOVAL FROM ALKALINE RADIOACTIVE WASTE SOLUTIONS

International Nuclear Information System (INIS)

Smith, F.; Hamm, Luther; Aleman, Sebastian; Michael, Johnston

2008-01-01

The performance of spherical Resorcinol-Formaldehyde ion-exchange resin for the removal of cesium from alkaline radioactive waste solutions has been investigated through computer modeling. Cesium adsorption isotherms were obtained by fitting experimental data using a thermodynamic framework. Results show that ion-exchange is an efficient method for cesium removal from highly alkaline radioactive waste solutions. On average, two 1300 liter columns operating in series are able to treat 690,000 liters of waste with an initial cesium concentration of 0.09 mM in 11 days achieving a decontamination factor of over 50,000. The study also tested the sensitivity of ion-exchange column performance to variations in flow rate, temperature and column dimensions. Modeling results can be used to optimize design of the ion exchange system

Efficiency and mechanisms of Cd removal from aqueous solution by biochar derived from water hyacinth (Eichornia crassipes).

Science.gov (United States)

Zhang, Feng; Wang, Xin; Yin, Daixia; Peng, Bo; Tan, Changyin; Liu, Yunguo; Tan, Xiaofei; Wu, Shixue

2015-04-15

This study investigated the efficiency and mechanisms of Cd removal by biochar pyrolyzed from water hyacinth (BC) at 250-550 °C. BC450 out-performed the other BCs at varying Cd concentrations and can remove nearly 100% Cd from aqueous solution within 1 h at initial Cd ≤ 50 mg l(-1). The process of Cd sorption by BC450 followed the pseudo-second order kinetics with the equilibrium being achieved after 24 h with initial Cd ranging from 100 to 500 mg l(-1). The maximum Cd sorption capacity of BC450 was estimated to be 70.3 mg g(-1) based on Langmuir model, which is prominent among a range of low-cost sorbents. Based on the balance analysis between cations released and Cd sorbed onto BC450 in combination with SEM-EDX and XPS data, ion-exchange followed by surface complexation is proposed as the dominant mechanism responsible for Cd immobilization by BC450. In parallel, XRD analysis also suggested the formation of insoluble Cd minerals (CdCO3, Cd3P2, Cd3(PO4)2 and K4CdCl6) from either (co)-precipitation or ion exchange. Results from this study highlighted that the conversion of water hyacinth into biochar is a promising method to achieve effective Cd immobilization and improved management of this highly problematic invasive species. Copyright © 2015 Elsevier Ltd. All rights reserved.

Dust particle removal efficiency of a venturi scrubber

International Nuclear Information System (INIS)

Ali, Majid; Yan, Changqi; Sun, Zhongning; Gu, Haifeng; Mehboob, Khurram

2013-01-01

Highlights: ► Experimental and theoretical study of dust removal efficiency in venturi scrubber. ► Dust removal efficiency 99.5% is achieved at throat gas velocity 220 m/s. ► Results obtained from mathematical model concur well with experimental results. - Abstract: The venturi scrubber is one of the most efficient gas cleaning devices to remove the contaminated particles from gaseous stream during severe accident in nuclear power plant. This study is focused on the dust particle removal efficiency of the venturi scrubber experimentally and theoretically. The venturi scrubber encapsulates the dust particles in petite water droplets flowing into it. The water injected into the scrubber is in the form of water film. The study investigates the removal efficiency of venturi scrubber for throat gas velocities of 130, 165 and 200 m/s and liquid flow rates 0.3–1 m 3 /h, whereas dust concentration ranges between 0.1 and 1 g/m 3 . The hydrophobic titanium dioxide (TiO 2 ) particles having density 4.23 g/cm 3 and mean diameter of 1 μm are used as dust particles in this research. Filtration technique is used to measure the concentration of dust particles at inlet and outlet. Experimental results show that the removal efficiency is higher with the increase of throat gas velocity and liquid flow rate. A mathematical model is employed for the verification of experimental results. The model concurs well with the experimental results

Removal and adsorption characteristics of polyvinyl alcohol from aqueous solutions using electrocoagulation

Energy Technology Data Exchange (ETDEWEB)

Chou, Wei-Lung, E-mail: wlchou@sunrise.hk.edu.tw [Department of Safety, Health and Environmental Engineering, Hungkuang University, Sha-Lu, Taichung 433, Taiwan (China)

2010-05-15

The study was to investigate the performance of electrocoagulation (EC) for the efficient removal of polyvinyl alcohol (PVA) from aqueous solutions. Several parameters were evaluated to characterize the PVA removal efficiency, such as various electrode pairs, current densities, supporting electrolytes, temperatures, and initial electrolyte concentrations. The effects of the current density, supporting electrolyte, and temperature on the electrical energy consumption were also investigated. The experimental results indicate that a Fe/Al electrode pair is the optimum choice out of four different electrode pair combinations. The optimum current density, supporting electrolyte concentration, and temperature were found to be 5 mA cm{sup -2}, 0.008N NaCl, and 298 K, respectively. The PVA removal efficiency decreased with increasing in the initial concentrations. The kinetic studies indicated that the EC process was best described using pseudo-second-order kinetics. The experimental data were also compared to different adsorption isotherm models in order to describe the EC process. The adsorption of PVA was best fitted by the Langmuir adsorption isotherm model. Thermodynamic parameters such as the Gibbs free energy, enthalpy, and entropy indicated that the adsorption of PVA on metal hydroxides was feasible, spontaneous and endothermic in the temperature range of 288-318 K.

Removal and adsorption characteristics of polyvinyl alcohol from aqueous solutions using electrocoagulation

International Nuclear Information System (INIS)

Chou, Wei-Lung

2010-01-01

The study was to investigate the performance of electrocoagulation (EC) for the efficient removal of polyvinyl alcohol (PVA) from aqueous solutions. Several parameters were evaluated to characterize the PVA removal efficiency, such as various electrode pairs, current densities, supporting electrolytes, temperatures, and initial electrolyte concentrations. The effects of the current density, supporting electrolyte, and temperature on the electrical energy consumption were also investigated. The experimental results indicate that a Fe/Al electrode pair is the optimum choice out of four different electrode pair combinations. The optimum current density, supporting electrolyte concentration, and temperature were found to be 5 mA cm -2 , 0.008N NaCl, and 298 K, respectively. The PVA removal efficiency decreased with increasing in the initial concentrations. The kinetic studies indicated that the EC process was best described using pseudo-second-order kinetics. The experimental data were also compared to different adsorption isotherm models in order to describe the EC process. The adsorption of PVA was best fitted by the Langmuir adsorption isotherm model. Thermodynamic parameters such as the Gibbs free energy, enthalpy, and entropy indicated that the adsorption of PVA on metal hydroxides was feasible, spontaneous and endothermic in the temperature range of 288-318 K.

Malachite green "a cationic dye" and its removal from aqueous solution by adsorption

Science.gov (United States)

Raval, Nirav P.; Shah, Prapti U.; Shah, Nisha K.

2017-11-01

Adsorption can be efficiently employed for the removal of various toxic dyes from water and wastewater. In this article, the authors reviewed variety of adsorbents used by various researchers for the removal of malachite green (MG) dye from an aqueous environment. The main motto of this review article was to assemble the scattered available information of adsorbents used for the removal of MG to enlighten their wide potential. In addition to this, various optimal experimental conditions (solution pH, equilibrium contact time, amount of adsorbent and temperature) as well as adsorption isotherms, kinetics and thermodynamics data of different adsorbents towards MG were also analyzed and tabulated. Finally, it was concluded that the agricultural solid wastes and biosorbents such as biopolymers and biomass adsorbents have demonstrated outstanding adsorption capabilities for removal of MG dye.

Efficiency of manganese dioxide for the removal of antimony from aqueous solutions

International Nuclear Information System (INIS)

Hasany, S.M.; Najamuddin; Ikram, M.

1993-01-01

The sorption of antimony onto manganese dioxide from aqueous solution has been investigated as a function of shaking time, composition of electrolyte, concentration of sorbent and sorbate, Maximum sorption of antimony has been achieved from deionized water after 15 minutes shaking at 45 cm/sup 3/g/sup -1/ V/W ratio. The influence of different anions and cations on the sorption has also been examined. EDTA, tartrate, citrate and Fe(II) decreased the sorption significantly. Among the metal ions tested only Se (IV) has shown strong sorption than antimony whereas Co(II), Hf (IV) and Te(IV) indicated low sorption affinity under similar experimental conditions. The sorption of antimony was also tested by different isotherms. The data fitted only to Freyndlich and D-R models. The sorption capacity of 7.71 m mole g/sup -1/, mean energy of sorption of 8.9 kJ mole/sup -1/ and of B = 0.00632 mole/sup 2/kJ/sup -2/ have been system. It is concluded that manganese dioxide can be used for the removal of antimony from industrial effluents and for its recovery from very dilute solutions. The oxide can also be applied for the separation of antimony, selenium and arsenic from Te(IV). (author)

Fluoride removal from diluted solutions by Donnan dialysis using full factorial design

Energy Technology Data Exchange (ETDEWEB)

Boubakri, Ali; Helali, Nawel; Tlili, Mohamed; Amor, Mohamed Ben [Center of Researches and Water Technologies, Soliman (Turkey)

2014-03-15

Excessive fluoride concentration in potable water can lead to fluorosis of teeth and bones. In the present study, Donnan dialysis (DD) is applied for the removal of fluoride ions from diluted sodium fluoride solutions. A four factor two level (2{sup 4}) full factorial design was used to investigate the influence of different physico-chemical parameters on fluoride removal efficiency (Y{sub F}) and fluoride flux (J{sub F}) through anion exchange membrane. The statistical design determines factors which have the important effects on Donnan dialysis performance and studies all interactions among the considered parameters. The four significant factors were initial fluoride concentration, feed flow rate, temperature and agitation speed. The experimental results and statistical analysis show that the temperature and agitation speed have positive effects on fluoride removal efficiency and the initial fluoride concentration has a negative effect. In the case of fluoride flux, feed flow rate and initial concentration are the main effect and all factors have a positive effect. The interaction between studied parameters was not negligible on two responses. A maximum fluoride removal of 75.52% was obtained under optimum conditions and the highest value of fluoride flux obtained was 2.4 mg/cm{sup 2}·h. Empirical regression models were also obtained and used to predict the flux and the fluoride removal profiles with satisfactory results.

Efficiency of Electrocoagulation for Removal of Reactive Yellow 14 from Aqueous Environments

OpenAIRE

Ahmad Reza Yaria; Mostafa Alizadeh; Sara Hashemi; Hamed Biglari

2013-01-01

Background & Aims of the Study: Discharge of textile industry colored wastewater without enough treatment into natural water resources cause serious pollution. Most of the conventional wastewater treatment methods are not effective enough to remove these dyes from wastewater. In this study, efficiency of electrocoagulation process with iron electrodes for treatment of Reactive Yellow 14 dye from synthetic solution has been studied and concluded. Materials & Methods: This exper...

Efficient removal of perfluorooctane sulfonate from aqueous film-forming foam solution by aeration-foam collection.

Science.gov (United States)

Meng, Pingping; Deng, Shubo; Maimaiti, Ayiguli; Wang, Bin; Huang, Jun; Wang, Yujue; Cousins, Ian T; Yu, Gang

2018-07-01

Aqueous film-forming foams (AFFFs) used in fire-fighting are one of the main contamination sources of perfluorooctane sulfonate (PFOS) to the subterranean environment, requiring high costs for remediation. In this study, a method that combined aeration and foam collection was presented to remove PFOS from a commercially available AFFF solution. The method utilized the strong surfactant properties of PFOS that cause it to be highly enriched at air-water interfaces. With an aeration flow rate of 75 mL/min, PFOS removal percent reached 96% after 2 h, and the PFOS concentration in the collected foam was up to 6.5 mmol/L, beneficial for PFOS recovery and reuse. Increasing the aeration flow rate, ionic strength and concentration of co-existing surfactant, as well as decreasing the initial PFOS concentration, increased the removal percents of PFOS by increasing the foam volume, but reduced the enrichment of PFOS in the foams. With the assistance of a co-existing hydrocarbon surfactant, PFOS removal percent was above 99.9% after aeration-foam collection for 2 h and the enrichment factor exceeded 8400. Aeration-foam collection was less effective for short-chain perfluoroalkyl substances due to their relatively lower surface activity. Aeration-foam collection was found to be effective for the removal of high concentrations of PFOS from AFFF-contaminated wastewater, and the concentrated PFOS in the collected foam can be reused. Copyright © 2018 Elsevier Ltd. All rights reserved.

Evaluation of natural zeolite clinoptilolite efficiency for the removal of ammonium and nitrate from aquatic solutions

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Mozhdeh Murkani

2015-01-01

Full Text Available Background: Surface water and groundwater pollution with various forms of nitrogen such as ammonium and nitrate ions is one of the main environmental risks. The major objectives of this study were to evaluate the capacity of natural zeolite (clinoptilolite to remove NO3– and NH4+ from polluted water under both batch and column conditions. Methods: The laboratory batch and column experiments were conducted to investigate the feasibility of clinoptilolite as the adsorbent for removal of nitrate (NO3– and ammonium (NH4+ ions from aqueous solution. The effects of pH, clinoptilolite dosage, contact time, and initial metal ion concentration on NO3– and NH4+ removal were investigated in a batch system. Results: Equilibrium time for NO3– and NH4+ ions exchange was 60 minutes and the optimum adsorbent dosage for their removal was 1 and 2.5 g/L, respectively. The adsorption isotherm of reaction (r> 0.9 and optimum entered concentration of ammonium and nitrate (30 and 6.5 mg/L, respectively were in accordance with Freundlich isotherm model. The ammonium removal rate increased by 98% after increasing the contact time. Conclusion: Our findings confirmed that natural Clinoptilolite can be used as one of effective, suitable, and low-costing adsorbent for removing ammonium from polluted waters.

Removal of lindane from an aqueous solution by using aminopropyl silica gel-immobilized calix[6]arene.

Science.gov (United States)

Tor, Ali; Aydin, Mehmet Emin; Aydin, Senar; Tabakci, Mustafa; Beduk, Fatma

2013-11-15

An aminopropyl silica gel-immobilized calix[6]arene (C[6]APS) has been used for the removal of lindane from an aqueous solution in batch sorption technique. The C[6]APS was synthesized with p-tert-butylcalix[6]arene hexacarboxylate derivative and aminopropyl silica gel in the presence of N,N'-diisopropyl carbodiimide coupling reagent. The sorption study was carried out as functions of solution pH, contact time, initial lindane concentration, C[6]APS dosage and ionic strength of solution. The matrix effect of natural water samples on the sorption efficiency of C[6]APS was also investigated. Maximum lindane removal was obtained at a wide pH range of 2-8 and sorption equilibrium was achieved in 2h. The isotherm analysis indicated that the sorption data can be represented by both Langmuir and Freundlich isotherm models. Increasing ionic strength of the solutions increased the sorption efficiency and matrix of natural water samples had no effect on the sorption of lindane. By using multilinear regression model, regression equation was also developed to explain the effects of the experimental variables. Copyright © 2013 Elsevier B.V. All rights reserved.

Chitin/clay microspheres with hierarchical architecture for highly efficient removal of organic dyes.

Science.gov (United States)

Xu, Rui; Mao, Jie; Peng, Na; Luo, Xiaogang; Chang, Chunyu

2018-05-15

Numerous adsorbents have been reported for efficient removal of dye from water, but the high cost raw materials and complicated fabrication process limit their practical applications. Herein, novel nanocomposite microspheres were fabricated from chitin and clay by a simple thermally induced sol-gel transition. Clay nanosheets were uniformly embedded in a nanofiber weaved chitin microsphere matrix, leading to their hierarchical architecture. Benefiting from this unique structure, microspheres could efficiently remove methylene blue (MB) through a spontaneous physic-sorption process which fit well with pseudo-second-order and Langmuir isotherm models. The maximal values of adsorption capability obtained by calculation and experiment were 152.2 and 156.7 mg g -1 , respectively. Chitin/clay microspheres (CCM2) could remove 99.99% MB from its aqueous solution (10 mg g -1 ) within 20 min. These findings provide insight into a new strategy for fabrication of dye adsorbents with hierarchical structure from low cost raw materials. Copyright © 2018 Elsevier Ltd. All rights reserved.

Arsenic Removal from Aqueous Solutions by Salvadora persica Stem Ash

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Ferdos Kord Mostafapour

2013-01-01

Full Text Available Arsenic is a naturally occurring metalloid, which is widely distributed in nature and is regarded as the largest mass poisoning in history. In the present study, the adsorption potential of Salvadora persica (S. persica stem ash in a batch system for the removal of As(V from aqueous solutions was investigated. Isotherm studies were carried out to evaluate the effect of contact time (20–240 min, pH (2–11, initial arsenic concentration (50–500 μg/L, and adsorbent dose on sorption efficiency. Maximum removal efficiency of 98.33% and 99.32% was obtained at pH 6, adsorbent dosage 3.5 g/L, initial As(V concentration 500 μg/L, and contact time 80 and 60 min for S. persica stem ash at 300 °C and 500 °C, respectively. Also, the adsorption equilibriums were analyzed by the Langmuir and Freundlich isotherm models. Such equilibriums showed that the adsorption data was well fitted with the Freundlich isotherm model for S. persica stem ash at both 300 °C and 500 °C (R2=0.8983 and 0.9274, resp.. According to achieved results, it was defined that S. persica stem ash can be used effectively for As(V removal from the aqueous environment.

Enhancing the sorption efficiency of polystyrene by immobilizing MgO and its application for uranium (VI) removal from aqueous solutions

Energy Technology Data Exchange (ETDEWEB)

Elhefnawy, O.A.; Elabd, A.A. [Nuclear and Radiological Regulatory Authority (NRRA), Cairo (Egypt). Nuclear Safeguards and Physical Protection Dept.

2016-07-01

Magnesium oxide immobilized polystyrene (PS/MgO) was prepared by the thermal attachment method for the removal of U(VI) from aqueous solutions. PS/MgO was characterized by different techniques [scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD)]. The effects of pH, adsorbent amount, contact time, initial U(VI) concentration, temperature and co-existing cations on the removal process were investigated by using batch technique. The results showed that the maximum adsorption capacity was 163 (mg g{sup -1}) at pH 6 and 293 K. The adsorption kinetics of U(VI) onto PS/MgO followed pseudo-second order and intra-particle kinetic models. The adsorption isotherms obeyed the Freundlich isotherm model. The thermodynamic parameters show that the process is endothermic and spontaneous. PS/MgO is an attractive adsorbent for U(VI) removal from aqueous solutions due to its accessibility, low preparation cost and high removal capacity.

Energy efficient SO2 removal from flue gases using the method Wellman-Lord

International Nuclear Information System (INIS)

Dzhonova-Atanasova, D.; Razkazova-Velkova, E.; Ljutzkanov, L.; Kolev, N.; Kolev, D.

2013-01-01

Full text: Investigations on development of energy efficient technology for SO 2 removal from flue gases of combustion systems by using the method Wellman-Lord are presented. It is characterized by absorption of sulfur dioxide with sodium sulfite solution, which reacts to form sodium bisulfite. The absorber is a packed column with multiple stages. After evaporation of the solution, SO 2 and sodium sulfite are obtained. The latter is dissolved in water from condensation of the steam carrying SO 2 from the evaporator. The regenerated solution returns in the absorber. The SO 2 removed from the flue gases is obtained as a pure product for use in chemical, food or wine production. The data discussed in the literature sources on flue gas desulfurization demonstrate the predominance of the methods with lime or limestone as absorbent, due to higher capital investments associated with the method of Wellman-Lord. A technological and economical evaluation of this regenerative method is presented in comparison to the non-regenerative gypsum method, using data from the existing sources and our own experience from the development of an innovative gypsum technology. Three solutions are discussed for significant enhancement of the method efficiency on the basis of a considerable increasing of the SO 2 concentration in the saturated absorbent. The improved method uses about 40% less heat for absorbent regeneration, in comparison to the existing applications of the method Wellman-Lord, and gives in addition the possibility to regenerate 95% of the consumed heat for heating water streams to about 90°C. Moreover, the incorporation in the installation of our system with contact economizers of second generation, already in industrial application, enables utilization of the waste heat of the flue gases for district heating. The employment of this system also leads to significant decreasing of the NO x emissions. key words: SO 2 removal, flue gases, absorption

Removal of lead from aqueous solution by an efficient low cost biosorbent

Energy Technology Data Exchange (ETDEWEB)

Alam, Sultan; Ullah, Azmat; Khan, Mashooq; Sadiq, Mohammad [Univ. of Malakand, Chakdara (Pakistan). Dept. of Chemistry; Hussain, Zahid; Amin, Noorul [AWK Univ., Mardan (Pakistan). Dept. of Chemistry

2012-03-15

Removal of Pb(II) ion from aqueous solution on modified sawdust obtained from Morus alba was investigated. The sample was characterized by BET surface area, EDX, FTIR and Zeta potential technique. The surface contains carbonyl and hydroxyl functional groups which act as binding sites for Pb(II) ion. Adsorption kinetics of Pb(II) on sawdust was tested by pseudo first order, Elovich and parabolic diffusion kinetic equations. The adsorption data were found to fit to Freundlich, Langmuir and Tempkin isotherms. The rate of adsorption was high at high temperature. Thermodynamic parameters like {delta}H, {delta}S and {delta}G were calculated from the kinetic data. The positive values of {delta}S reflect some structural exchange among the active site of the adsorbent and metal ion. The negative values of Gibbs free energy ({delta}G) show the spontaneous nature of the process. (orig.)

Activation of Graphene Oxide with Hydrochloric Acid for Nitrate Removal from Aqueous Solutions

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Abolghasem Alighardashi

2017-11-01

Full Text Available Long-term drinking of nitrate-contaminated water poses a serious risk to human health. The present study explores the possibility of enhancing the adsorption capacity of graphene oxide via activation with hydrochloric acid for nitrate removal from aqueous solutions. Experiments were performed in a batch reactor in which such major factors as pH, reaction time, and concentrations of both graphene oxide (GO and activated graphene oxide (AGO were used as variables. Nitrate removal efficiency was investigated using the One-Way ANOVA statistical test and SPSS-16 software. The chemical composition and solid structure of the synthesized AGO were analyzed using FE-SEM coupled with energy dispersive spectrometry (EDS. The micropore volumes of the samples were determined using the BET and BJH. The predominant composition (52% of the synthesized AGO was C and its mean pore diameter was 26.896 nm. The maximum adsorption capacity of AGO was estimated at 3333.33 mg/g. Based on the results, the AGO nano-structure may be recomended as a new means for nitrate removal from aqueous solutions.

Evaluation of sorptive flotation technique for enhanced removal of radioactive Eu(III) from aqueous solutions

Energy Technology Data Exchange (ETDEWEB)

Ezzat, Amir; Saad, Ebtissam A. [Ain Shams Univ., Cairo (Egypt). Chemistry Dept.; Mahmoud, Mamdoh R. [Atomic Energy Authority, Cairo (Egypt). Nuclear Chemistry Dept.; Soliman, Mohamed A. [Atomic Energy Authority, Cairo (Egypt). Egypt Second Research Reactor; Kandil, Abdelhakim [Helwan Univ., Cairo (Egypt). Chemistry Dept.

2017-06-01

The present study aims at the removal of Eu(III) from aqueous solutions by sorptive flotation process. This process involves adsorption of Eu(III) onto bentonite and kaolinite clays followed by floatation using sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB) collectors. The effect of adsorption parameters (pH, contact time, clay weight, Eu(III) concentration, ionic strength) as well as flotation parameters (collector and frother concentrations, bubbling time, concentrations of foreign cations and anions) on the removal efficiency of Eu(III) were studied. The obtained results show that Eu(III) ions are removed efficiently (R% ∝ 95%) at pH=4 after 1 h shaking with clay and 15 min floatation. The adsorption kinetics of Eu(III) onto the employed clays followed the pseudo-second-order model and the equilibrium data fitted well to the Freundlich isotherm model.

Removal of Cr(VI from Aqueous Solutions Using mino-fuctionalized Nanoporous MCM-41

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Farshid Ghorbani

2016-09-01

Full Text Available An amino-functionalized nanoporous material was prepared by grafting 3-aminopropyl trimethoxysilane (APTMS group onto MCM-41. The as-synthesized material was characterized by X-ray diffraction (XRD analysis, nitrogen adsorption-desorption measurements (BET, thermogravimetric analysis (TGA, and Fourier transform infrared spectrometry (FTIR to confirm the ordered mesoporous structure and the functionalization of the amino group. The NH2-MCM-41 thus obtained was employed as the sorbent to remove Cr(VI ions from aqueous solutions. The batch adsorption process was carried out to evaluate the effects of solution pH, adsorbent dosage, metal ion concentration, and temperature. Results revealed that removal efficiency increased to a maximum of 124 mg.g‒1 and metal uptake decreased (0.1 g.l‒1 with increasing sorbent dosage from 0.1 to 3.5 g.l‒1. A reverse trend was, however, observed with increasing Cr(VI concentration. It was also found that a pH equal to 3 was the optimum level for the removal of Cr(VI ions from aqueous solutions. Thermodynamic examinations revealed the strong dependence of the adsorption process on temperature such that adsorption capacity increased with increasing temperature, indicating the endothermic and spontaneous nature of the adsorption process.

Efficiency of final irrigation of root canal in removal of smear layer

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Mitić Aleksandar

2009-01-01

Full Text Available Introduction A smear layer forms on the root canal walls as the consequence of root instrumentation. The smear layer formed in such a way considerably influences the quality of root obturation and endodontic treatment outcome. Objective The aim of this study was to ultrastructurally analyze the surface of intracanal dentine after removal of the smear layer by the solution of doxycycline, citric acid and detergent Tween-80 (MTAD. Methods The study involved 60 single-rooted, extracted, human teeth divided into four groups. All samples were instrumented by a step-back technique and manual K-files, and rinsed during instrumentation by 2% CHX and H2O2. The first group of samples was exclusively rinsed by CHX and H2O2; in the second group, besides using CHX and H2O2, MTAD solution was used for the final irrigation. The samples which were rinsed by distilled water (+ control and the samples rinsed by 5.25% NaOCl and 17% Na EDTA (-control served as control groups. All samples were observed under the scanning electronic microscope JEOL-JSM-5300. The coronary, middle and apex thirds of the radix region were analyzed. Results The obtained results of the SEM analysis showed that the application of 2% chlorhexidine and hydrogen peroxide did not give clear dentine walls, and the smear layer could not be removed completely. The application of the same combination (CHX and H2O2, added by the final MTAD irrigation solution, led to the efficient removal of the smear layer, while the morphological structure of dentine surface remained unchanged. Statistical analysis showed that canal walls in the experimental group with MTAD as the final irrigation were significantly clearer compared to the control group (p<0.001. Conclusion Based on the obtained results, it can be concluded that MTAD is an efficient solution for the final irrigation of the canal system.

Poorly crystalline hydroxyapatite: A novel adsorbent for enhanced fulvic acid removal from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Wei, Wei [Department of Environmental Science and Engineering, Nanjing Normal University, Nanjing 210023 (China); Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, Nanjing Normal University, Nanjing 210023 (China); Jiangsu Center for Collaborative Innovation in Geographical Information Resource Development and Application, Nanjing Normal University, Nanjing 210023 (China); Yang, Lei; Zhong, Wenhui; Cui, Jing [Department of Environmental Science and Engineering, Nanjing Normal University, Nanjing 210023 (China); Wei, Zhenggui, E-mail: weizhenggui@gmail.com [Department of Environmental Science and Engineering, Nanjing Normal University, Nanjing 210023 (China); Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, Nanjing Normal University, Nanjing 210023 (China); Jiangsu Center for Collaborative Innovation in Geographical Information Resource Development and Application, Nanjing Normal University, Nanjing 210023 (China)

2015-03-30

Graphical abstract: - Highlights: • Poorly crystalline HAP was firstly used for FA removal from aqueous solution. • The maximum adsorption capacity was determined to be 90.20 mg/g at 318 K. • Adsorption kinetics, isotherms and thermodynamic have been studied in detail. • Adsorption mechanism involved surface complexation, electrostatic interaction and hydrogen bonding. - Abstract: In this study, poorly crystalline hydroxyapatite (HAP) was developed as an efficient adsorbent for the removal of fulvic acid (FA) from aqueous solution. Surface functionality, crystallinity, and morphology of the synthetic adsorbent were studied by Fourier-transformation infrared (FT-IR) spectroscopy, powder X-ray diffraction (XRD) and transmission electron microscopy (TEM). The effects of various parameters such as crystallinity of adsorbent, contact time, adsorbent dosage, pH, initial adsorbate concentration, temperature, ionic strength and the presence of alkaline earth metal ions on FA adsorption were investigated. Results indicated that the nanosized HAP calcined at lower temperature was poorly crystalline (X{sub c} = 0.23) and had better adsorption capacity for FA than those (X{sub c} = 0.52, 0.86) calcined at higher temperature. FA removal was increased with increases of adsorbent dosage, temperature, ionic strength and the presence of alkali earth metal ions, but decreased as the pH increased. Kinetic studies showed that pseudo-second-order kinetic model better described the adsorption process. Equilibrium data were best described by Sips models, and the estimated maximum adsorption capacity of poorly crystalline HAP was 90.20 mg/g at 318 K, displaying higher efficiency for FA removal than previously reported adsorbents. FT-IR results revealed that FA adsorption over the adsorbent could be attributed to the surface complexation between the oxygen atom of functional groups of FA and calcium ions of HAP. Regeneration studies indicated that HAP could be recyclable for a long

Removal of insecticide carbofuran from aqueous solutions by banana stalks activated carbon

International Nuclear Information System (INIS)

Salman, J.M.; Hameed, B.H.

2010-01-01

In this work, activated carbon was prepared from banana stalks (BSAC) waste to remove the insecticide carbofuran from aqueous solutions. The effects of contact time, initial carbofuran concentration, solution pH and temperature (30, 40 and 50 deg. C) were investigated. Adsorption isotherm, kinetics and thermodynamics of carbofuran on BSAC were studied. Equilibrium data were fitted to the Langmuir, Freundlich and Temkin isotherm models and the data best represented by the Langmuir isotherm. Thermodynamic parameters such as standard enthalpy (ΔH o ), standard entropy (ΔS o ) and standard free energy (ΔG o ) were evaluated. Regeneration efficiency of spent BSAC was studied using ethanol as a solvent. The efficiency was found to be in the range of 96.97-97.35%. The results indicated that the BSAC has good regeneration and reusability characteristics and can be used as alternative to present commercial activated carbon.

Antimony removal from aqueous solutions using Zirconium hydroxide

International Nuclear Information System (INIS)

Petrescu, D.; Velciu, L.; Bucur, C.

2016-01-01

In this paper it is presented an experimental test for non-radioactive antimony removal from aqueous solutions using zirconium hydroxide powder. Also, it was studied how the temperature and pH influences antimony adsorption onto zirconium hydroxide surface. After the adsorption, solutions were filtered on Cellulose Mixed Ester Membrane with 0.2 μm pore size to remove the zirconium powder and then the aqueous solutions were sent to Inductively Coupled Plasma Optic Emission Spectrometry (ICP-OES) for quantitative analysis of Sb. Zirconium hydroxide powders were examined by optical microscopy. For the solutions that were tested at pH 4.5 and 10.2 the antimony concentration dropped below the detection limit of ICP-OES device, proof of antimony adsorption on zirconium hydroxide. Also, for the other tested solutions which had pH=12 the antimony concentration reduced with 77% and 80%. The temperature had no influence upon adsorption mechanism. (authors)

High Efficient Nanocomposite for Removal of Heavy Metals (Hg2+ and Pb2+ from Aqueous Solution

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M. Ebadi

2016-01-01

Full Text Available In current work, CdS/black carbon nanocomposites were successfully synthesized with the aid of chestnut and cadmium nitrate as the starting reagents. Besides, the effects of preparation parameters such as reaction time, and precursor concentration on the morphology of products and removal of heavy metals (Hg+2, Pb+2 were studied by scanning electron microscopy images and batch adsorption mode. CdS/black carbon nanocomposite introduced as new and high efficient system for removal of heavy metal ions. The as-synthesized products were characterized by powder X-ray diffraction, scanning electron microscopy, and spectra energy dispersive analysis of X-ray.

Inorganic sorbents for radiostrontium removal from waste solutions: selectivity and role of calixarenes

International Nuclear Information System (INIS)

Vijayan, S.; Belikov, K.; Drapailo, A.

2011-01-01

The challenge in the remediation of 90 Sr-contaminated waters arises from the need to achieve very high removal efficiencies to meet discharge targets from waste effluents containing relatively high concentrations of non-radioactive cations. Low-cost natural zeolites are not selective for strontium over other divalent cations, notably such ions as calcium; and produce low 90 Sr removal performance, and large volumes of spent sorbent waste. The synthesis and use of selective, synthetic inorganic sorbents could prove to be a feasible approach for high 90 Sr removal efficiencies, and much smaller volumes of secondary solid waste generation. The essential advantages of inorganic sorbents include their stability and resistance to radiation, and the potential for producing stable waste forms such as vitrified glass or ceramics for disposal. However, the cost of strontium-specific sorbents is prohibitive for large-scale applications at present. This paper is a review of the reported information on removal mechanisms and performance of Sr-specific inorganic sorbents. The analysis has revealed promising performance, efficiency and selectivity for strontium removal from solutions containing low and high concentrations of salts. The leading sorbents are crystalline silicotitanate and oxides of metals such as titanium. An initial assessment has also been made of the performance of calixarene-based macrocyclic compounds. These are known for their selectivity for strontium in solvent extraction processes. From the initial strontium removal results in bench-scale tests using different solid substrates, impregnated with calixarene derivatives, only sodium-mordenite impregnated with calyx[8]arene octamide gave an overall strontium removal efficiency in the range of 90 to 95% in the presence of 3.5 ppm calcium. There was no improvement observed for strontium-removal efficiency or selectivity over calcium in the calixarene-impregnated inorganic sorbent matrix. In several tests, the

A new alternative adsorbent for the removal of cationic dyes from aqueous solution

Directory of Open Access Journals (Sweden)

T. Santhi

2016-09-01

Full Text Available Adsorption of Malachite green (MG and Methylene blue (MB from aqueous solutions on low cost adsorbent prepared from Annona squmosa seed (CAS is studied experimentally. Results obtained indicate that the removal efficiency of Malachite green and Methylene blue at 27 ± 2 °C exceeds 75.66% and 24.33% respectively, and that the adsorption process is highly pH-dependent. Results showed that the optimum pH for dye removal is 6.0. The amount of dye adsorbed from aqueous solution increases with the increase of the initial dye concentration. Smaller adsorbent particle adds to increase the percentage removal of Malachite green and Methylene blue. The equilibrium data fitted well to the Langmuir model (R2 > 0.97 and the adsorption kinetic followed the pseudo-second-order equation (R2 > 0.99. The maximum adsorption capacities of MG, MB on CAS are 25.91 mg g−1 and 08.52 mg g−1 respectively. These results suggest that A. squmosa seed is a potential low-cost adsorbent for the dye removal from industrial wastewater. The adsorption capacity of CAS on MG is greater than MB.

Removal of phosphorus from aqueous solution by Posidonia oceanica fibers using continuous stirring tank reactor

Energy Technology Data Exchange (ETDEWEB)

Wahab, Mohamed Ali, E-mail: waheb_med@yahoo.fr [University of Carthage, Water Research and Technologies Centre (CERTE), Wastewater Treatment and Recycling Laboratory, B.P. 273, 8020 Soliman (Tunisia); Hassine, Rafik Ben [International Environmental Green Technology (IGET) (Tunisia); Jellali, Salah, E-mail: salah.jallali@certe.rnrt.tn [University of Carthage, Water Research and Technologies Centre (CERTE), Wastewater Treatment and Recycling Laboratory, B.P. 273, 8020 Soliman (Tunisia)

2011-05-15

The present study aims to develop a new potentially low-cost, sustainable treatment approach to soluble inorganic phosphorus removal from synthetic solutions and secondary wastewater effluents in which a plant waste (Posidonia oceanica fiber: POF) is used for further agronomic benefit. Dynamic flow tests using a continuous stirred tank reactor (CSTR) were carried out to study the effect of initial concentration of phosphorus, amount of adsorbent, feeding flow rate and anions competition. The experimental results showed that the removal efficiency of phosphorus from synthetic solutions is about 80% for 10 g L{sup -1} of POF. In addition, the variation of the initial concentration of phosphorus from 8 to 50 mg L{sup -1} increased the adsorption capacity from 0.99 to 3.03 mg g{sup -1}. The use of secondary treated wastewater showed the presence of competition phenomenon between phosphorus and sulphate which could be overcoming with increasing the sorptive surface area and providing more adsorption sites when increasing the adsorbent dosage of POF. Compared with columns studies, this novel CSTR system showed more advantages for the removal of soluble phosphorus as a tertiary treatment of urban secondary effluents with more adsorption efficiency and capacity, in addition to the prospect use of saturated POF with nutriment as fertilizer and compost.

Removal of phosphorus from aqueous solution by Posidonia oceanica fibers using continuous stirring tank reactor

International Nuclear Information System (INIS)

Wahab, Mohamed Ali; Hassine, Rafik Ben; Jellali, Salah

2011-01-01

The present study aims to develop a new potentially low-cost, sustainable treatment approach to soluble inorganic phosphorus removal from synthetic solutions and secondary wastewater effluents in which a plant waste (Posidonia oceanica fiber: POF) is used for further agronomic benefit. Dynamic flow tests using a continuous stirred tank reactor (CSTR) were carried out to study the effect of initial concentration of phosphorus, amount of adsorbent, feeding flow rate and anions competition. The experimental results showed that the removal efficiency of phosphorus from synthetic solutions is about 80% for 10 g L -1 of POF. In addition, the variation of the initial concentration of phosphorus from 8 to 50 mg L -1 increased the adsorption capacity from 0.99 to 3.03 mg g -1 . The use of secondary treated wastewater showed the presence of competition phenomenon between phosphorus and sulphate which could be overcoming with increasing the sorptive surface area and providing more adsorption sites when increasing the adsorbent dosage of POF. Compared with columns studies, this novel CSTR system showed more advantages for the removal of soluble phosphorus as a tertiary treatment of urban secondary effluents with more adsorption efficiency and capacity, in addition to the prospect use of saturated POF with nutriment as fertilizer and compost.

Efficient removal of chromate and arsenate from individual and mixed system by malachite nanoparticles

International Nuclear Information System (INIS)

Saikia, Jiban; Saha, Bedabrata; Das, Gopal

2011-01-01

Graphical abstract: Malachite nanoparticles of 100-150 nm, have been efficiently and for the first time used as an adsorbent for the removal of toxic arsenate and chromate in pH range 4-5. - Abstract: Malachite nanoparticles of 100-150 nm have been efficiently and for the first time used as an adsorbent for the removal of toxic arsenate and chromate. We report a high adsorption capacity for chromate and arsenate on malachite nanoparticle from both individual and mixed solution in pH ∼4-5. However, the adsorption efficiency decreases with the increase of solution pH. Batch studies revealed that initial pH, temperature, malachite nanoparticles dose and initial concentration of chromate and arsenate were important parameters for the adsorption process. Thermodynamic analysis showed that adsorption of chromate and arsenate on malachite nanoparticles is endothermic and spontaneous. The adsorption of these anions has also been investigated quantitatively with the help of adsorption kinetics, isotherm, and selectivity coefficient (K) analysis. The adsorption data for both chromate and arsenate were fitted well in Langmuir isotherm and preferentially followed the second order kinetics. The binding affinity of chromate is found to be slightly higher than arsenate in a competitive adsorption process which leads to the comparatively higher adsorption of chromate on malachite nanoparticles surface.

Improvement of the Separation Efficiency of Ion Flotation and Adsorbing Colloid Flotation by the Synergistic Effect of Mixed Surfactant Solutions

Energy Technology Data Exchange (ETDEWEB)

Kim, K.H.; Seo, E.J.; Choi, S.J. [Dept. of. Env. Eng., Kyungpook National University, Taegu (Korea)

1999-02-01

Experimental investigations on the removal of Cd(II) from aqueous ablution were carried out through two foam separation techniques : ion floatation and adsorbing colloid flotation with Fe(III). The optimum pH for good removal was found to be about 6.4 for the former and about 11 for the latter. The effect of flotation time. pH, surfactant(sodium lauryl sulfate), foreign ions(Na{sup +}, Ca{sup 2+}, No{sub 3}{sup -}, SO{sub 2}{sup -4} ) on the efficiency of Cd(II) removal were discussed. The presence of foreign ions inhibit the Cd(II) removal by foam flotation. It was suggested that the limitation of foam flotation on Cd(II) removal may be overcome by the surface activity of mixed surfactant solution. The application of the synergistic effect of mixed surfactant solutions to the improvement of the removal efficiency of foam flotation was experimentally verified in this work. 19 refs., 7 figs., 3 tabs.

Application of Electrocoagulation Process for Reactive Red 198 Dye Removal from the Aqueous Solution

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Mansooreh Dehghani

2014-04-01

Full Text Available Abstract Background and purpose:The main objectives of this research were to evaluating the application of electrocoagulation process for 198 dye from the aqueous phase and determining the optimum operating conditions to the dye removal using aluminum and iron electrodes. Materials and Methods:The present study was conducted in bench-scale. The spectrophotometer DR 5000 was used to determine the dye concentration. The effects of pH, retention time, voltage, dye concentration on the efficiency of electrocoagulation process were investigated. Data were analyzed in SPSS for Windows 16.0 using Pearson’scorrelation coefficient to analyze the relationship between these parameters. Results:The results showed that the optimal conditions for reactive red 198 (RR-198 dye removal from the aqueous solution are pH of 11, the voltage of 32 V, the initial dye concentration of 10 ppm, and the reaction time of 40 min. Pearson correlation analysis showed that there is a significant relationship between voltage and the reaction time with the removal efficiencies (P< 0.01. Conclusion:It was revealed that the removal efficiency of dye was directly proportional to the voltage and reaction time, but inversely proportional to the initial dye concentration. In conclusion, electrocoagulation process using two-fold iron and aluminum electrodes is an appropriate method for reducing the RR-198 dye in the aqueous phase.

Removal of Arsenic (V) from Aqueous Solutions Using Chitosan-Red Scoria and Chitosan-Pumice Blends.

Science.gov (United States)

Asere, Tsegaye Girma; Mincke, Stein; De Clercq, Jeriffa; Verbeken, Kim; Tessema, Dejene A; Fufa, Fekadu; Stevens, Christian V; Du Laing, Gijs

2017-08-09

In different regions across the globe, elevated arsenic contents in the groundwater constitute a major health problem. In this work, a biopolymer chitosan has been blended with volcanic rocks (red scoria and pumice) for arsenic (V) removal. The effect of three blending ratios of chitosan and volcanic rocks (1:2, 1:5 and 1:10) on arsenic removal has been studied. The optimal blending ratio was 1:5 (chitosan: volcanic rocks) with maximum adsorption capacity of 0.72 mg/g and 0.71 mg/g for chitosan: red scoria (Ch-Rs) and chitosan: pumice (Ch-Pu), respectively. The experimental adsorption data fitted well a Langmuir isotherm ( R ² > 0.99) and followed pseudo-second-order kinetics. The high stability of the materials and their high arsenic (V) removal efficiency (~93%) in a wide pH range (4 to 10) are useful for real field applications. Moreover, the blends could be regenerated using 0.05 M NaOH and used for several cycles without losing their original arsenic removal efficiency. The results of the study demonstrate that chitosan-volcanic rock blends should be further explored as a potential sustainable solution for removal of arsenic (V) from water.

Removal of copper ions from aqueous solutions by means of micellar-enhanced ultrafiltration

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Kowalska Izabela

2017-01-01

Full Text Available The aim of the study was to assess the usefulness of micellar–enhanced ultrafiltration (MEUF for removal of copper ions from water solutions in comparison with classic ultrafiltration process. The tests were conducted in a semi–pilot membrane installation with the use of ultrafiltration module KOCH/ROMICON® at a transmembrane pressure of 0.05 MPa. The effect of concentration of copper ions on ultrafiltration process efficiency was investigated. The second part of the tests concerned the removal of copper ions by MEUF under wide range of anionic surfactant concentration (0.25, 1, and 5 CMC (critical micelle concentration. Concentration of copper ions in model solutions was equal to 5, 20, and 50 mg Cu/L. Furthermore, the effect of surfactant leakage to the permeate side during filtration was evaluated. Conducted experiments confirmed effectiveness of MEUF in copper ions removal. For the highest copper concentration in the feed (i.e. 50 mg/L, the average concentration of copper ions in the permeate ranged from 1.2–4.7 mg Cu/L depending on surfactant concentration. During filtration experiments, UF module exhibited stable transport properties for model solutions containing copper. For the highest concentration of metal, the decrease of permeate flux did not exceed 11% after 60 minutes of filtration. In the presence of the surfactant, a slight deterioration of transport properties was observed.

Efficiency of Acacia Tortillis Plant Pod Shell as a Low Cost and Available Adsorbent for the Removal of Phenol

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Hossien JafariMansoorian

2015-05-01

Full Text Available The presence of nondegradable toxic compounds such as phenol in the environment has nowadays led to many health and environmental problems. The present empirical study was conducted on the lab scale to evaluate the efficiency of Acacia tortillis pod shell as a new alternative and low cost adsorbent for removing phenol from aqueous solutions. The experiment was performed in a batch system and the effects of important operation variables including initial phenol concentrations of 0.5, 1, 2, 4, 8, 16, 32, and 64 mg/l, absorbent doses of 0.1, 0.2, 0.4, 0.8, and 1.6g/l in predetermined mesh sizes (ranging over 30-60 and 60-100, pH levels of 2, 4, 6, 8, 10, and 12, and contact times of 10, 20, 30, 40, 50, and 60 min were evaluated. Finally, the Freundlich and Langmuir adsorption isotherms were determined in order to describe the relationship between the colored solution and the absorbent. Results showed that the highest phenol absorption efficiency achieved was above 95% which was obtained with an optimum pH level of 2, an optimum absorbent dose of 0.2 g/l, and a mesh size of 60-100 for a contact time of 10 minutes and at a low pollutant concentration. Increasing phenol concentration increased its removal efficiency but this removal rate was lower at extreme concentrations. Also, the adsorption process was found to be more compatible with the Freundlich model. Based on the results obtained, the pod shells of Acacia tortillis pod shell may be claimed to be an effective, efficient, and cheap absorbent for the removal of phenol from aqueous solutions.

Highly efficient removal of perfluorooctanoic acid from aqueous solution by H2O2-enhanced electrocoagulation-electroflotation technique

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Bo Yang

2016-03-01

Full Text Available Electrocoagulation (EC technique was used to investigate the removal performance of aqueous perfluorooctanoic acid (PFOA with relatively high concentration as simulating the wastewater from organic fluorine industry. A comparison was done with the similar amount of coagulant between EC and chemical coagulation process. PFOA removal obtained was higher with EC process, especially for Fe anode. Several factors were studied to optimize the EC process. At the optimal operating parameters including 37.5 mA/cm2 of current density, initial pH 3.77, and 180 rpm of mixing speed, 93% of PFOA could be removed with 100 mg/L of initial concentration after 90-min electrolysis. Furthermore, the remove efficiency could be obviously improved by H2O2 intermittent addition, which removed more than 99% of PFOA within 40-min EC. It could be attributed to that H2O2 facilitated the oxidative transformation from ferrous to ferric ion. In addition, the adsorptive removal of aqueous PFOA on Fe flocs during EC was also verified by fourier transform infrared spectra.

Efficient removal of sulfur hexafluoride (SF6) through reacting with recycled electroplating sludge.

Science.gov (United States)

Zhang, Jia; Zhou, Ji Zhi; Liu, Qiang; Qian, Guangren; Xu, Zhi Ping

2013-06-18

This paper reports that recycled electroplating sludge is able to efficiently remove greenhouse gas sulfur hexafluoride (SF6). The removal process involves various reactions of SF6 with the recycled sludge. Remarkably, the sludge completely removed SF6 at a capacity of 1.10 mmol/g (SF6/sludge) at 600 °C. More importantly, the evolved gases were SO2, SiF4, and a limited amount of HF, with no toxic SOF4, SO2F2, or SF4 being detected. These generated gases can be readily captured and removed by NaOH solution. The reacted solids were further found to be various metal fluorides, thus revealing that SF6 removal takes place by reacting with various metal oxides and silicate in the sludge. Moreover, the kinetic investigation revealed that the SF6 reaction with the sludge is a first-order chemically controlled process. This research thus demonstrates that the waste electroplating sludge can be potentially used as an effective removal agent for one of the notorious greenhouse gases, SF6.

Removal of heavy metals from synthetic solution by electrocoagulation

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Mohamed Ilou

2016-05-01

Full Text Available The objective of this work concerns the optimization of the operating conditions for the removal of heavy metals from synthetic solution by Electrocoagulation (EC. To reach this purpose, we prepared a synthetic wastewater containing certain heavy metals (Ni, Cu, Zn, Fe and Pb to study the influence of various parameters (conductivity, pH, time of electrolysis, current density and the initial concentration of the metal on the rate of removal of these metals. The results show that this rate of removal can reach 99.9 % in the following optimal conditions: pH included between 6 and 8 and a density of the current of 1~1.5A / dm2. This study shows that it is possible to remove metals in aqueous solution by the technique of electrocoagulation. 

Removal of Hexavalent Chromium from Aqueous Solution by Modified Holly Sawdust: A Study of Equilibrium and Kinetics

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S. Azizian

2010-01-01

Full Text Available Introduction & Objective: Industrial wastewaters including heavy metals, are among the important sources of environmental pollution. Heavy metals such as chromium are found in plating wastewater and is harmful for human health and environment. The purpose of the present study was to investigate the absorption of heavy metals such as chromium onto modified holly sawdust as an cheaper absorbent. Materials & Methods: This study was a fundamental- application study done in Hamadan University of Medical Sciences, hygiene faculty water and wastewater chemistry laboratory. This study investigated the removal of hexavalent chromium by using modified holly sawdust with pH changes ,contact time ,absorbent dose and Cr(VI concentrations in batch system. Then the result was analyzed by Excel software.Results: The results showed that the removal efficiency decrease is accompanied by the increase of pH and initial chromium concentration. pH increase from 2 to 12(equilibrium time= 180 min, adsorbent dose= 0.6g/100CC, Cr(VI concentrations= 60 mg/L,leaded to the removal efficiency decrease from 99.67 % to 29.78 %. Also removal efficiency decreased from 99.37 % to 40.24 % after increasing the initial chromium concentrations from 20 mg/L to 100 mg/L. Moreover the results showed the removal efficiency increased after increasing the adsorbent dose and contact time. By increasing adsorbent dose from 0.2 g/100CC to 1 g/100CC, the removal efficiency increased from 34.65 % to 99.76 %.Additionally, the removal efficiency increased from 48.53%to 99.76% by increasing contact time from 5 mins to 180 mins. Experimental isotherms and kinetics models were assessed by Langmuir and Freundlich isotherms and pseudo-first-order and pseudo-second-order kinetics models. The results showed that the data were acceptably explained acceptably by Langmuir isotherms and pseudo-second-order kinetics models respectively.Conclusion: The results showed that the removal of hexavalent chromium

Removal of iron contaminant from zirconium chloride solution

International Nuclear Information System (INIS)

Voit, D.O.

1992-01-01

This patent describes a process for eliminating iron contaminant from an aqueous zirconium chloride solution that has been contaminated with FeCl 3 in a plant in which zirconium and hafnium chloride solutions are separated by a main MINK solvent extraction system and the FeCl 3 is normally removed from the zirconium chloride solution by a secondary MINK solvent extraction system

A novel compound cleaning solution for benzotriazole removal after copper CMP

International Nuclear Information System (INIS)

Gu Zhangbing; Liu Yuling; Gao Baohong; Wang Chenwei; Deng Haiwen

2015-01-01

After the chemical mechanical planarization (CMP) process, the copper surface is contaminated by a mass of particles (e.g. silica) and organic residues (e.g. benzotriazole), which could do great harm to the integrated circuit, so post-CMP cleaning is essential. In particular, benzotriazole (BTA) forms a layer of Cu-BTA film with copper on the surface, which leads to a hydrophobic surface of copper. So an effective cleaning solution is needed to remove BTA from the copper surface. In this work, a new compound cleaning solution is designed to solve two major problems caused by BTA: one is removing BTA and the other is copper surface corrosion that is caused by the cleaning solution. The cleaning solution is formed of alkaline chelating agent (FA/O II type), which is used to remove BTA, and a surfactant (FA/O I type), which is used as a corrosion inhibitor. BTA removal is characterized by contact angle measurements and electrochemical techniques. The inhibiting corrosion ability of the surfactant is also characterized by electrochemical techniques. The proposed compound cleaning solution shows advantages in removing BTA without corroding the copper surface. (paper)

Preparation of low cost activated carbon from Myrtus communis and pomegranate and their efficient application for removal of Congo red from aqueous solution

Science.gov (United States)

Ghaedi, Mehrorang; Tavallali, Hossein; Sharifi, Mahdi; Kokhdan, Syamak Nasiri; Asghari, Alireza

2012-02-01

In this research, the potential applicability of activated carbon prepared from Myrtus communis (AC-MC) and pomegranate (AC-PG) as useful adsorbents for the removal of Congo red (CR) from aqueous solutions in batch method was investigated. The effects of pH, contact time, agitation time and amount of adsorbents on removal percentage of Congo red on both adsorbents were examined. Increase in pH up to 6 for AC-MC and pH 7 for AC-PG increase the adsorption percentage (capacity) and reach equilibrium within 30 min of contact time. Fitting the experimental data to conventional isotherm models like Freundlich, Langmuir, Tempkin and Dubinin-Radushkevich show that the experimental data fitted very well to the Freundlich isotherm for AC-MC and Langmuir isotherm for AC-PG. Fitting the experimental data to different kinetic models such as pseudo first-order, pseudo second-order, Elovich and intraparticle diffusion mechanism showed the applicability of a pseudo second-order with involvement of intraparticle diffusion model for interpretation of experimental data for both adsorbents. The adsorption capacity of AC-PG and AC-MC for the removal of CR was found to be 19.231 and 10 mg g -1. These results clearly indicate the efficiency of adsorbents as a low cost adsorbent for treatment of wastewater containing CR.

Removal of Cd+2 from aqueous solutions onto polypyrrole coated reticulated vitreous carbon eletrodes

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Tramontina Jucelânia

2001-01-01

Full Text Available The development of simple methods for removal of heavy metals from aqueous samples is a relevant field of research. In this connection, the electrodeposition of the Cd+2 ion, one of the most toxic species for animals and human beings, was investigated in aerated pH 4.8 sulfuric-sulfate solutions. In potentiostatic conditions, the maximum rate of cadmium deposition at a neutral polypyrrole (PPy0 coated reticulated vitreous carbon (RVC working electrode occurs at -3.0 V vs. the saturated calomel reference electrode (SCE. Moreover, the conversion rate depends both on the applied potential and on the mass transport regime, and, for solutions containing 10 mg L-1 of Cd2+, the highest removal efficiency achieved is 84% after 90 min of electrolysis. The concentration decay of the Cd+2 ion in the solution was monitored by anodic stripping voltammetry (ASV at a hanging mercury drop electrode. Besides, metallic cadmium deposited onto the polypyrrole modified RVC electrode was evidenced by Scanning Electron Microscopy (SEM analysis using the backscattered electron image (BEI technique and by Energy Dispersive Spectrometry (EDS.

Improving energy efficiency in industrial solutions - Walk the talk

Energy Technology Data Exchange (ETDEWEB)

Wegener, D. (Siemens AG. Industry Solutions Div., Erlangen (Germany)); Finkbeiner, M. (Technische Univ. Berlin (TUB). Sustainable Engineering, Berlin (Germany)); Holst, J.-C.; Walachowicz, F. (Siemens AG. Corporate Technology, Berlin (Germany)); Irving Olsen, S. (Technical Univ. of Denmark (DTU). Management Engineering, Kgs. Lyngby (Denmark))

2011-05-15

This paper describes the outline of the energy efficiency and environmental care policy and management at Siemens Industry Solutions Division. This environmental policy coherently embraces strategic planning, eco-design of energy-efficient industrial processes and solutions, design evaluation and finally communication of both environmental and economic performance of solutions to customers. One of the main tools supporting eco-design and evaluation and controlling of derived design solutions is the so called 'Eco-Care-Matrix' (ECM). The ECM simply visualizes the eco-efficiency of solutions compared to a given baseline. In order to prevent from 'green washing' criticism and to ensure 'walk the talk' attitude the ECM should be scientifically well-founded using appropriate and consistent methodology. The vertical axis of an ECM illustrates the environmental performance and the horizontal axis describes the economical customer benefit of one or more green solutions compared to a defined reference solution. Different scientific approaches for quantifying the environmental performance based on life cycle assessment methodology are discussed especially considering the ISO standards 14040/14044:2006. Appropriate ECM application is illustrated using the example of the Siemens MEROS technology (Maximized Emission Reduction of Sintering) for the steel industry. MEROS is currently the most modern and powerful system for cleaning off-gas in sinter plants. As an environmental technology MEROS is binding and removing sulfur dioxide and other acidic gas components present in the off-gas stream by using dry absorbents and additional electrical power. Advantage in the impact category of acidification potential (by desulfurization) is a trade-off to disadvantages in global warming and resource depletion potential caused by use of electricity. Representing different impacts, indicator results for impact categories with different tendencies have to be

Simultaneous removal and recovery of uranium from aqueous solution using TiO_2 photoelectrochemical reduction method

International Nuclear Information System (INIS)

Huichao He; Meirong Zong; Faqin Dong; Southwest University of Science and Technology, Sichuan; Pengpan Yang; Gaili Ke; Mingxue Liu; Xiaoqin Nie; Wei Ren; Liang Bian; Southwest University of Science and Technology, Sichuan; Chinese Academy of Sciences, Xinjiang

2017-01-01

U(VI)-containing wastewater has potential radiation hazard to the environment, but contains valuable uranium resource. Based on the reduction of U(VI) and the difference in solubility between U(VI) and U(IV), here we construct a TiO_2-based photoelectrochemical cell to remove U(VI) and recover uranium from aqueous solution. By irradiating TiO_2 photoanode at E = 0.45 V versus SCE, U(VI) can be simultaneously removed from aqueous solution and recovered as solid uranium compounds on a FTO glass cathode. Since ethanol can act as hole scavenger to protect the formed U(IV) and provide CO_2"−"· as reductant, ethanol adding improved the U(VI) reduction efficiency of TiO_2-based photoelectrochemical cell. (author)

Poorly crystalline hydroxyapatite: A novel adsorbent for enhanced fulvic acid removal from aqueous solution

Science.gov (United States)

Wei, Wei; Yang, Lei; Zhong, Wenhui; Cui, Jing; Wei, Zhenggui

2015-03-01

In this study, poorly crystalline hydroxyapatite (HAP) was developed as an efficient adsorbent for the removal of fulvic acid (FA) from aqueous solution. Surface functionality, crystallinity, and morphology of the synthetic adsorbent were studied by Fourier-transformation infrared (FT-IR) spectroscopy, powder X-ray diffraction (XRD) and transmission electron microscopy (TEM). The effects of various parameters such as crystallinity of adsorbent, contact time, adsorbent dosage, pH, initial adsorbate concentration, temperature, ionic strength and the presence of alkaline earth metal ions on FA adsorption were investigated. Results indicated that the nanosized HAP calcined at lower temperature was poorly crystalline (Xc = 0.23) and had better adsorption capacity for FA than those (Xc = 0.52, 0.86) calcined at higher temperature. FA removal was increased with increases of adsorbent dosage, temperature, ionic strength and the presence of alkali earth metal ions, but decreased as the pH increased. Kinetic studies showed that pseudo-second-order kinetic model better described the adsorption process. Equilibrium data were best described by Sips models, and the estimated maximum adsorption capacity of poorly crystalline HAP was 90.20 mg/g at 318 K, displaying higher efficiency for FA removal than previously reported adsorbents. FT-IR results revealed that FA adsorption over the adsorbent could be attributed to the surface complexation between the oxygen atom of functional groups of FA and calcium ions of HAP. Regeneration studies indicated that HAP could be recyclable for a long term. Findings of the present work highlight the potential for using poorly crystalline HAP nanoparticles as an effective and recyclable adsorbent for FA removal from aqueous solution.

Temperature dependent fission product removal efficiency due to pool scrubbing

Energy Technology Data Exchange (ETDEWEB)

Uchida, Shunsuke, E-mail: suchida@iae.or.jp [Institute of Applied Energy, 1-14-2, Nishi-Shimbashi, Minato-ku, Tokyo 105-0003 (Japan); Itoh, Ayumi; Naitoh, Masanori; Okada, Hidetoshi; Suzuki, Hiroyuki [Institute of Applied Energy, 1-14-2, Nishi-Shimbashi, Minato-ku, Tokyo 105-0003 (Japan); Hanamoto, Yukio [KAKEN, Inc., 1044, Hori-machi, Mito 310-0903 (Japan); Osakabe, Masahiro [Tokyo University of Marine Science & Technology, Koutou-ku, Tokyo 135-8533 (Japan); Fujikawa, Masahiro [Japan Broadcasting Corporation, 2-2-1, Jinnan, Shibuya-ku, Tokyo 150-8001 (Japan)

2016-03-15

Highlights: • Pool temperature effects on the FP removal were not clearly concluded in the previous publications. • It was confirmed that the removal efficiency decreased with temperature around the boiling point. • A modified empirical formula for FP removal was proposed as a function of sub-cooling temperature. • DF could be predicted with an accuracy within a factor of 2 with the proposed formula. - Abstract: The wet-well of boiling water reactors plays important roles not only to suppress the pressure in the primary containment vessel due to steam scrubbing effects during severe accidents but also to mitigate release of radioactive fission products (FP), aerosols and particulates, into the environment. The effects of steam scrubbing in the wet-well on FP removal have been well studied and reported by changing major parameters determining the removal efficiencies, e.g., aerosol diameters, submergence (depth of scrubbing nozzles) and steam/non-condensable gas volume fraction. Unfortunately, the effects of pool temperature on the FP removal were not clearly concluded in the previous publications, though it would be easily expected that boiling in the pool resulted in reduced aerosol removal efficiency. In order to determine the temperature effects on FP removal efficiency, amounts of cesium in aerosols released from scrubbing pool were measured by changing pool temperature in mini and medium scale scrubbing experiments, and then, it was confirmed that the removal efficiency clearly decreased with temperature around the boiling point. Then, a modified empirical formula to express the FP removal around the boiling point temperature was proposed as a function of sub-cooling temperature by applying the effective steam volume fraction, which was designated as the volume ratio of condensed steam in the pool versus the sum of input steam and non-condensable gas. By comparing the measured removal efficiency with the calculated, it was validated that the

Temperature dependent fission product removal efficiency due to pool scrubbing

International Nuclear Information System (INIS)

Uchida, Shunsuke; Itoh, Ayumi; Naitoh, Masanori; Okada, Hidetoshi; Suzuki, Hiroyuki; Hanamoto, Yukio; Osakabe, Masahiro; Fujikawa, Masahiro

2016-01-01

Highlights: • Pool temperature effects on the FP removal were not clearly concluded in the previous publications. • It was confirmed that the removal efficiency decreased with temperature around the boiling point. • A modified empirical formula for FP removal was proposed as a function of sub-cooling temperature. • DF could be predicted with an accuracy within a factor of 2 with the proposed formula. - Abstract: The wet-well of boiling water reactors plays important roles not only to suppress the pressure in the primary containment vessel due to steam scrubbing effects during severe accidents but also to mitigate release of radioactive fission products (FP), aerosols and particulates, into the environment. The effects of steam scrubbing in the wet-well on FP removal have been well studied and reported by changing major parameters determining the removal efficiencies, e.g., aerosol diameters, submergence (depth of scrubbing nozzles) and steam/non-condensable gas volume fraction. Unfortunately, the effects of pool temperature on the FP removal were not clearly concluded in the previous publications, though it would be easily expected that boiling in the pool resulted in reduced aerosol removal efficiency. In order to determine the temperature effects on FP removal efficiency, amounts of cesium in aerosols released from scrubbing pool were measured by changing pool temperature in mini and medium scale scrubbing experiments, and then, it was confirmed that the removal efficiency clearly decreased with temperature around the boiling point. Then, a modified empirical formula to express the FP removal around the boiling point temperature was proposed as a function of sub-cooling temperature by applying the effective steam volume fraction, which was designated as the volume ratio of condensed steam in the pool versus the sum of input steam and non-condensable gas. By comparing the measured removal efficiency with the calculated, it was validated that the

Synthesis of Ce(III)-doped Fe3O4 magnetic particles for efficient removal of antimony from aqueous solution

International Nuclear Information System (INIS)

Qi, Zenglu; Joshi, Tista Prasai; Liu, Ruiping; Liu, Huijuan; Qu, Jiuhui

2017-01-01

Highlights: • Doping of Ce into Fe 3 O 4 was achieved based on a facile solvothermal method. • After doping, the removal capacity was increased by 5 times for “Sb(V)” and 2 times for “Sb(III)”. • Decreasing pH improved adsorption of Sb(V) but decreased adsorption of Sb(III). • Antimony sorption mechanisms on Ce-doped Fe 3 O 4 were illustrated. - Abstract: Aqueous antimony (Sb) pollution from human activity is of great concern in drinking water due to its adverse health effect. Magnetic Fe 3 O 4 particles, with high separation ability from solution, have been considered as a low-cost Sb adsorbent for contaminants. However, the limited adsorption capacity has restricted its practical application. In this study, a solvothermal approach was developed for doping Ce(III) into Fe 3 O 4 , thereby increasing the adsorption efficacy for both Sb(III) and Sb(V). In contrast to un-doped Fe 3 O 4 , the adsorption capacity towards Sb(III) and Sb(V) in Ce-doped materials increased from 111.4 to 224.2 mg/g and from 37.2 to 188.1 mg/g at neutral pH, respectively. Based on the combined results of XPS, XRD, and FTIR, it confirmed that Ce atom successfully doped into the Fe 3 O 4 structure, resulting in the decreased particle size, increased the surface area, and isoelectric point. Furthermore, the vibrating sample magnetometer (VSM) results showed that the Ce doping process had some side effects on the primitive magnetic property, but remaining the high separation potential during water treatment. According to the high removal efficiency and magnetic property, the Ce-doped Fe 3 O 4 of great simplicity should be a promising adsorbent for aqueous Sb removal.

Boron removal from geothermal waters by electrocoagulation

Energy Technology Data Exchange (ETDEWEB)

Yilmaz, A. Erdem [Atatuerk University, Faculty of Engineering, Department of Environmental Engineering., 25240 Erzurum (Turkey)], E-mail: aerdemy@atauni.edu.tr; Boncukcuoglu, Recep [Atatuerk University, Faculty of Engineering, Department of Environmental Engineering., 25240 Erzurum (Turkey); Kocakerim, M. Muhtar [Atatuerk University, Faculty of Engineering, Department of Chemical Engineering, 25240 Erzurum (Turkey); Yilmaz, M. Tolga; Paluluoglu, Cihan [Atatuerk University, Faculty of Engineering, Department of Environmental Engineering., 25240 Erzurum (Turkey)

2008-05-01

Most of the geothermal waters in Turkey contain extremely high concentration of boron when they are used for irrigation. The use of geothermal waters for irrigation can results in excess amount deposition of boron in soil. On the other hand, a minimal boron concentration is required for irrigational waters. In this study, electrocoagulation (EC) was selected as a treatment process for the removal of boron from thermal waters obtained from Ilica-Erzurum in Turkey. Current density (CD), pH of solution and temperature of solution were selected as operational parameters. The results showed that boron removal efficiency increased from pH 4.0 to 8.0 and decreased at pH 10.0. Although boron removal efficiency was highest at pH 8.0, energy consumption was very high at this pH value compared to other pH intervals. Boron removal efficiency reached to 95% with increasing current density from 1.5 to 6.0 mA/cm{sup 2}, but energy consumption was also increased in this interval. At higher temperatures of solution, such as 313 and 333 K, boron removal efficiency increased. At optimum conditions, boron removal efficiency in geothermal water reached up to 95%.

Boron removal from geothermal waters by electrocoagulation

International Nuclear Information System (INIS)

Yilmaz, A. Erdem; Boncukcuoglu, Recep; Kocakerim, M. Muhtar; Yilmaz, M. Tolga; Paluluoglu, Cihan

2008-01-01

Most of the geothermal waters in Turkey contain extremely high concentration of boron when they are used for irrigation. The use of geothermal waters for irrigation can results in excess amount deposition of boron in soil. On the other hand, a minimal boron concentration is required for irrigational waters. In this study, electrocoagulation (EC) was selected as a treatment process for the removal of boron from thermal waters obtained from Ilica-Erzurum in Turkey. Current density (CD), pH of solution and temperature of solution were selected as operational parameters. The results showed that boron removal efficiency increased from pH 4.0 to 8.0 and decreased at pH 10.0. Although boron removal efficiency was highest at pH 8.0, energy consumption was very high at this pH value compared to other pH intervals. Boron removal efficiency reached to 95% with increasing current density from 1.5 to 6.0 mA/cm 2 , but energy consumption was also increased in this interval. At higher temperatures of solution, such as 313 and 333 K, boron removal efficiency increased. At optimum conditions, boron removal efficiency in geothermal water reached up to 95%

Dye and its removal from aqueous solution by adsorption: a review.

Science.gov (United States)

Yagub, Mustafa T; Sen, Tushar Kanti; Afroze, Sharmeen; Ang, H M

2014-07-01

In this review article the authors presented up to-date development on the application of adsorption in the removal of dyes from aqueous solution. This review article provides extensive literature information about dyes, its classification and toxicity, various treatment methods, and dye adsorption characteristics by various adsorbents. One of the objectives of this review article is to organise the scattered available information on various aspects on a wide range of potentially effective adsorbents in the removal of dyes. Therefore, an extensive list of various adsorbents such as natural materials, waste materials from industry, agricultural by-products, and biomass based activated carbon in the removal of various dyes has been compiled here. Dye bearing waste treatment by adsorption using low cost alternative adsorbent is a demanding area as it has double benefits i.e. water treatment and waste management. Further, activated carbon from biomass has the advantage of offering an effected low cost replacement for non-renewable coal based granular activated carbon provided that they have similar or better adsorption on efficiency. The effectiveness of various adsorbents under different physico-chemical process parameters and their comparative adsorption capacity towards dye adsorption has also been presented. This review paper also includes the affective adsorption factors of dye such as solution pH, initial dye concentration, adsorbent dosage, and temperature. The applicability of various adsorption kinetic models and isotherm models for dye removal by wide range of adsorbents is also reported here. Conclusions have been drawn from the literature reviewed and few suggestions for future research are proposed. Copyright © 2014 Elsevier B.V. All rights reserved.

The investigation of parameters affecting boron removal by electrocoagulation method

International Nuclear Information System (INIS)

Yilmaz, A. Erdem; Boncukcuoglu, Recep; Kocakerim, M. Muhtar; Keskinler, Buelent

2005-01-01

Boron removal from wastewaters by electrocoagulation using aluminum electrode material was investigated in this paper. Several working parameters, such as pH, current density, boron concentration and type and concentration of supporting electrolyte were studied in an attempt to achieve a higher removal capacity. The experiments were carried out by keeping the pH of solution constant and optimum pH of solution was determined 8.0 for the aluminum electrode. Although energy consumption increased with decreasing boron concentration, which conductivity of these solutions were low, boron removal efficiency was higher at 100 mg/L than that of 1000 mg/L. Current density was an important parameter affecting removal efficiency. Boron removal efficiency and energy consumption increased with increasing current density from 1.2 to 6.0 mA/cm 2 . The types of different supporting electrolyte were experimented in order to investigate to this parameter effect on boron removal. The highest boron removal efficiency, 97%, was found by CaCl 2 . Added CaCl 2 increased more the conductivity of solution according to other supporting electrolytes, but decreased energy consumption. The results showed to have a high effectiveness of the electrocoagulation method in removing boron from aqueous solutions

A quantitative comparison between electrocoagulation and chemical coagulation for boron removal from boron-containing solution

International Nuclear Information System (INIS)

Yilmaz, A. Erdem; Boncukcuoglu, Recep; Kocakerim, M. Muhtar

2007-01-01

This paper provides a quantitative comparison of electrocoagulation and chemical coagulation approaches based on boron removal. Electrocoagulation process delivers the coagulant in situ as the sacrificial anode corrodes, due to a fixed current density, while the simultaneous evolution of hydrogen at the cathode allows for pollutant removal by flotation. By comparison, conventional chemical coagulation typically adds a salt of the coagulant, with settling providing the primary pollutant removal path. Chemical coagulation was carried out via jar tests using aluminum chloride. Comparison was done with the same amount of coagulant between electrocoagulation and chemical coagulation processes. Boron removal obtained was higher with electrocoagulation process. In addition, it was seen that chemical coagulation has any effect for boron removal from boron-containing solution. At optimum conditions (e.g. pH 8.0 and aluminum dose of 7.45 g/L), boron removal efficiencies for electrocoagulation and chemical coagulation were 94.0% and 24.0%, respectively

A quantitative comparison between electrocoagulation and chemical coagulation for boron removal from boron-containing solution

Energy Technology Data Exchange (ETDEWEB)

Yilmaz, A. Erdem [Atatuerk University, Faculty of Engineering, Department of Environmental Engineering, 25240 Erzurum (Turkey)], E-mail: aerdemy@atauni.edu.tr; Boncukcuoglu, Recep [Atatuerk University, Faculty of Engineering, Department of Environmental Engineering, 25240 Erzurum (Turkey); Kocakerim, M. Muhtar [Atatuerk University, Faculty of Engineering, Department of Chemical Engineering, 25240 Erzurum (Turkey)

2007-10-22

This paper provides a quantitative comparison of electrocoagulation and chemical coagulation approaches based on boron removal. Electrocoagulation process delivers the coagulant in situ as the sacrificial anode corrodes, due to a fixed current density, while the simultaneous evolution of hydrogen at the cathode allows for pollutant removal by flotation. By comparison, conventional chemical coagulation typically adds a salt of the coagulant, with settling providing the primary pollutant removal path. Chemical coagulation was carried out via jar tests using aluminum chloride. Comparison was done with the same amount of coagulant between electrocoagulation and chemical coagulation processes. Boron removal obtained was higher with electrocoagulation process. In addition, it was seen that chemical coagulation has any effect for boron removal from boron-containing solution. At optimum conditions (e.g. pH 8.0 and aluminum dose of 7.45 g/L), boron removal efficiencies for electrocoagulation and chemical coagulation were 94.0% and 24.0%, respectively.

Fixed bed column study for Cu (II) removal from aqueous solution using water hyacinth (Eichornia crassipes) biomass.

Science.gov (United States)

Gandhimathi, R; Ramesh, S T; Yadu, Anubhav; Bharathi, K S

2013-07-01

This paper reports the results of the study on the performance of low-cost biosorbent water hyacinth (WH) in removing Cu (II) from aqueous solution. The adsorbent material adopted was found to be an efficient media for the removal of Cu (II) in continuous mode using fixed bed column. The column studies were conducted with 10 mg/L metal solution with a flow rate of 10 mL/min with different bed depths such as 10, 20 and 30 cm. The column design parameters like adsorption rate constant, adsorption capacity and minimum bed depth were calculated. It was found that, the adsorption capacity of copper ions by water hyacinth increased by increasing the bed depth and the contact time.

Highly Efficient Interception and Precipitation of Uranium(VI) from Aqueous Solution by Iron-Electrocoagulation Combined with Cooperative Chelation by Organic Ligands.

Science.gov (United States)

Li, Peng; Zhun, Bao; Wang, Xuegang; Liao, PingPing; Wang, Guanghui; Wang, Lizhang; Guo, Yadan; Zhang, Weimin

2017-12-19

A new strategy combining iron-electrocoagulation and organic ligands (OGLs) cooperative chelation was proposed to screen and precipitate low concentrations (0-18.52 μmol/L) of uranium contaminant in aqueous solution. We hypothesized that OGLs with amino, hydroxyl, and carboxyl groups hydrophobically/hydrophilically would realize precuring of uranyl ion at pH electrocoagulation would achieve faster and more efficient uranium precipitation. Experimentally, the strategy demonstrated highly efficient uranium(VI) precipitation efficiency, especially with hydrophilic macromolecular OGLs. The uranium removal efficiency at optimized experimental condition reached 99.65%. The decrease of zeta potential and the lattice enwrapping between U-OGLs chelates and flocculation precursor were ascribed to the enhanced uranium precipitation activity. Uranium was precipitated as oxides of U(VI) or higher valences that were easily captured in aggregated micelles under low operation current potential. The actual uranium tailing wastewater was treated, and a satisfied uranium removal efficiency of 99.02% was discovered. After elution of the precipitated flocs, a concentrated uranium solution (up to 106.52 μmol/L) with very few other metallic impurities was obtained. Therefore, the proposed strategy could remove uranium and concentrate it concurrently. This work could provide new insights into the purification and recovery of uranium from aqueous solutions in a cost-effective and environmentally friendly process.

Removal of nitrate, ammonia and phosphate from aqueous solutions in packed bed filter using biochar augmented sand media

Directory of Open Access Journals (Sweden)

El Hanandeh Ali

2017-01-01

Full Text Available Nutrients from wastewater are a major source of pollution because they can cause significant impact on the ecosystem. Accordingly, it is important that the nutrient concentrations are kept to admissible levels to the receiving environment. Often regulatory limits are set on the maximum allowable concentrations in the effluent. Therefore, wastewater must be treated to meet safe levels of discharge. In this study, laboratory investigation of the efficiency of packed bed filters to remove nitrate, ammonium and phosphate from aqueous solutions were conducted. Sand and sand augmented with hydrochloric acid treated biochar (SBC were used as packing media. Synthetic wastewater solution was prepared with PO43−, NO3−, NH4+ concentrations 20, 10, 50 mg/L, respectively. Each experiment ran for a period of five days; samples from the effluent were collected on alternate days. All experiments were duplicated. Over the experiment period, the average removal efficiency of PO43−, NO3−, NH4+ were 99.2%, 72.9%, 96.7% in the sand packed columns and 99.2%, 82.3%, 97.4% in the SBC packed columns, respectively. Although, the presence of biochar in the packing media had little effect on phosphate and ammonium removal, it significantly improved nitrate removal.

Removal of uranium from ammonium nitrate solution by nanofiltration

Energy Technology Data Exchange (ETDEWEB)

Wang, Runci; Yuan, Zhongwei; Yan, Taihong; Zheng, Weifang [China Institute of Atomic Energy, Beijing (China). Dept. of Radiochemistry

2017-07-01

Two types of nanofiltration membranes were tested to remove uranium dissolved in ammonium nitrate solution, and the influence of operating parameters as transmembrane pressure, tangential velocity and feed temperature was investigated. Experimental results showed NF270 membrane can reject more than 96% uranium and allow most (90% min) ammonium nitrate solution passed by, and with a permeate flux of 60 L/(m{sup 2}.h). Nanofiltration seems to be a promising technology for the removal of uranium and recovery of ammonium nitrate simultaneously.

Enhanced removal of radioactive particles by fluorocarbon surfactant solutions

International Nuclear Information System (INIS)

Kaiser, R.; Harling, O.K.

1993-08-01

The proposed research addressed the application of ESI's particle removal process to the non-destructive decontamination of nuclear equipment. The cleaning medium used in this process is a solution of a high molecular weight fluorocarbon surfactant in an inert perfluorinated liquid which results in enhanced particle removal. The perfluorinated liquids of interest, which are recycled in the process, are nontoxic, nonflammable, and environmentally compatible, and do not present a hazard to the ozone layer. The information obtained in the Phase 1 program indicated that the proposed ESI process is technically effective and economically attractive. The fluorocarbon surfactant solutions used as working media in the ESI process survived exposure of up to 10 Mrad doses of gamma rays, and are considered sufficiently radiation resistant for the proposed process. Ultrasonic cleaning in perfluorinated surfactant solutions was found to be an effective method of removing radioactive iron (Fe 59) oxide particles from contaminated test pieces. Radioactive particles suspended in the process liquids could be quantitatively removed by filtration through a 0.1 um membrane filter. Projected economics indicate a pre-tax pay back time of 1 month for a commercial scale system

Effects of additives on 2,4,6-trinitrotoluene (TNT) removal and its mineralization in aqueous solution by gamma irradiation

International Nuclear Information System (INIS)

Lee, Byungjin; Jeong, Seung-Woo

2009-01-01

The effects of additives (i.e., methanol, EDTA, mannitol, thiourea, nitrous oxide, oxygen and ozone) on gamma irradiation of 2,4,6-trinitrotoluene (TNT) were investigated to elucidate the initial reaction mechanism of TNT degradation and suggest an practical method for complete by-product removal. All additives, except thiourea, significantly increased the TNT removal efficiency by gamma irradiation. The overall results of the additive experiments implied that the TNT decomposition would be initiated by ·OH, e aq - , and HO 2 ·/O 2 · - , and also implied that ·H did not have any direct effect on the TNT decomposition. Additions of methanol and nitrous oxide were more effective in TNT removal than the other additives, achieving complete removal of TNT at doses below 20 kGy. Total organic carbon (TOC) of the irradiated solution was analyzed to evaluate the degree of TNT mineralization under the additive conditions. TOC under the nitrous oxide addition was removed rapidly, and complete TNT mineralization was thus achieved at 50 kGy. Methanol addition was very effective in the TNT removal, but it was not effective in reduction in TOC. Trinitrobenzene (TNB), oxalic acid and glyoxalic acid were detected as radiolytic organic by-products, while ammonia and nitrate were detected as radiolytic inorganic by-products. The most efficient TNT removal and its mineralization by gamma irradiation would be achieved by supersaturating the solution with nitrous oxide before irradiation.

The removal of actinide metals from solution

International Nuclear Information System (INIS)

Hancock, R.D.; Howell, I.V.

1980-01-01

A process is specified for removing actinide metals (e.g. uranium) from solutions. The solution is contacted with a substrate comprising the product obtained by reacting an inorganic solid containing surface hydroxyl groups (e.g. silica gel) with a compound containing a silane grouping, a nitrogen-containing group (e.g. an amine) and other specified radicals. After treatment, the actinide metal is recovered from the substrate. (U.K.)

Removal of As(V, Cr(VI and Pb(II from aqueous solution using surfactant-modified Sabzevar nanozeolite

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Kourosh Razmgar

2016-04-01

Full Text Available The pollution of water environments is a challenging issue especially in developing countries. Contamination of drinking water with heavy metals has been reported in many parts of the world. Arsenic, chromium and lead are dangerous heavy metals and also common contaminants of drinking water. In this study, the capacity and performance of the surfactant-modified Sabzevar natural nanozeolite (SMSNZ on the removal of heavy metals from an aqueous solution was investigated. Initially, the appropriate concentration of hexadecyltrimethylammonium bromide HDTMA-Br solution for modification was investigated; it was found that it must be higher than the critical concentration micelle (CMC. Then, the removal of As (V, Cr (VI, and Pb(II from an aqueous solution was studied using SMSNZ. The results indicated that the removal efficiency was very high in different initial concentrations of heavy metals. The Linear, Langmuir and Freundlich isotherm models were used to investigate the adsorption equilibrium of the surfactant-modified natural zeolite for heavy metals adsorption. The results showed that the Linear isotherm is a better fit for the three studied heavy metals.

Protein-bound solute removal during extended multipass versus standard hemodialysis

DEFF Research Database (Denmark)

Eloot, Sunny; Van Biesen, Wim; Axelsen, Mette

2015-01-01

and middle molecules compared to standard hemodialysis (SHD). Since protein-bound solutes (PBS) exert important pathophysiological effects, we investigated whether MPHD results in improved removal of PBS as well. METHODS: A cross-over study (Clinical Trial NCT01267760) was performed in nine stable HD......), hippuric acid (HA), indole acetic acid (IAA), indoxyl sulfate (IS), and p-cresylsulfate (PCS). Dialyser extraction ratio, reduction ratio, and solute removal were calculated for these solutes. RESULTS: Already at 60 min after dialysis start, the extraction ratio in the hemodialyser was a factor 1.4-4 lower...

Highly efficient removal of trace thallium from contaminated source waters with ferrate: Role of in situ formed ferric nanoparticle.

Science.gov (United States)

Liu, Yulei; Wang, Lu; Wang, Xianshi; Huang, Zhuangsong; Xu, Chengbiao; Yang, Tao; Zhao, Xiaodan; Qi, Jingyao; Ma, Jun

2017-11-01

Thallium (Tl) is highly toxic to mammals and relevant pollution cases are increasing world-widely. Convenient and efficient method for the removal of trace Tl from contaminated source water is imperative. Here, the removal of trace Tl by K 2 FeO 4 [Fe(VI)] was investigated for the first time, with the exploration of reaction mechanisms. Six different types of water treatment agents (powdered activated carbon, Al 2 (SO 4 ) 3 , FeCl 3 , δ-MnO 2 , MnO 2 nano-particles, and K 2 FeO 4 ) were used for the removal of Tl in spiked river water, and K 2 FeO 4 showed excellent removal performance. Over 92% of Tl (1 μg/L) was removed within 5 min by applying 2.5 mg/L of K 2 FeO 4 (pH 7.0, 20 °C). XPS analysis revealed that in the reaction of Tl(I) with K 2 FeO 4 , Tl(I) was oxidized to Tl(III), and removed by the K 2 FeO 4 reduced ferric particles. The removal of Tl by in situ formed and ex situ formed ferric particle was examined respectively, and the results revealed that the removal of trace Tl could be attributed to the combination of adsorption and coprecipitation processes. The hydrodynamic size of the reduced particle from K 2 FeO 4 ranged from 10 nm to 100 nm, and its surface was negatively charged under neutral pH condition. These factors were conducive for the efficient removal of Tl by K 2 FeO 4 . The effects of solution pH, coexisting ions (Na + , Ca 2+ , and HCO 3 - ), humic acid, solution temperature, and reductive environment on the removal and desorption of Tl were investigated, and the elimination of Tl in polluted river water and reservoir water was performed. These results suggest that K 2 FeO 4 could be an efficient and convenient agent on trace Tl removal. Copyright © 2017. Published by Elsevier Ltd.

Removal of thorium(IV) from aqueous solutions by natural sepiolite

Energy Technology Data Exchange (ETDEWEB)

Erden, Kadriye Esen [Pamukkale Univ., Denizli (Turkey). Dept. of Electricity and Energy; Donat, Ramazan [Pamukkale Univ., Denizli (Turkey). Dept. of Chemistry

2017-06-01

Natural sepiolite has been tested as a potential sorbent for the removal of Th(IV) from aqueous solutions by batch technique. Effects of various parameters on the adsorption process have been investigated. Under optimum conditions, Th(IV) was adsorbed with high adsorption efficiency. The results indicated that sorption of Th(IV) on sepiolite was strongly affected by pH values and temperature. The adsorption patterns of thorium on the sepiolite adsorbent followed the Langmuir, Freundlich and Dubinin-Radushkevich (D-R) isotherms. The thermodynamic data (ΔH , ΔS , ΔG ) are calculated from the temperature-dependent sorption isotherms. The results suggest that sorption process of Th(IV) on sepiolite is spontaneous and endothermic.

Assessment of Some Synthetic Polymers for the Removal of Pollutants from Waste Solutions

International Nuclear Information System (INIS)

Ayoub, R.; El-Naggar, H.A.; Ezz EL-Din, M.R.; Moussa, A.R.

1999-01-01

The sorption capacity of 134 Cs, 60 Co, 152+154 Eu and Cu (II) by three prepared has been studied using batch and column techniques. The three polymers are polyacrylic acid (PAA), polyacrylamide-acrylic acid (PAM-AA) and polyacrylamide-N-vinyl-2-pyrraldone (PAM-NVP). These polymers were prepared by gamma radiation initiated polymerization of their corresponding monomer solutions. The appropriate value for V/m ratio (volume of solution to mass of polymer) that can result in reasonably high distribution coefficient, Kd, was determined. The variation of the amount sorbed of the isotope per gram polymer (X/m) with concentration of the relevant element was found to follow a Frendlich type isotherm. The distribution coefficient, Kd, of the studied element was found to be affected by the ph of the solution. The desorption of the investigated metal ions is also studied at different ph. For column studies, the percent removed of the radioisotopes 134 Cs, 60 Co, ( 152+154 )Eu in addition to some heavy metals ions such as Pb, Cd, Zn and Cu(II) was determined. More than 95% of these elements were removed when 3 beds column of PAA or PAM-AA was used. From the data obtained we can conclude that the polymer PAA or PAM-AA can considered as an efficient sorbent for metal cations from their aqueous solution

Removal of trace mercury (II) from aqueous solution by in situ MnO(x) combined with poly-aluminum chloride.

Science.gov (United States)

Lu, Xixin; Huangfu, Xiaoliu; Zhang, Xiang; Wang, Yaan; Ma, Jun

2015-06-01

Removal of trace mercury from aqueous solution by Mn (hydr)oxides formed in situ during coagulation with poly-aluminum chloride (PAC) (in situ MnO(x) combined with PAC) was investigated. The efficiency of trace mercury removal was evaluated under the experimental conditions of reaction time, Mn dosage, pH, and temperature. In addition, the ionic strength and the initial mercury concentration were examined to evaluate trace mercury removal for different water qualities. The results clearly demonstrated that in situ MnO(x) combined with PAC was effective for trace mercury removal from aqueous solution. A mercury removal ratio of 9.7 μg Hg/mg Mn was obtained at pH 3. Furthermore, at an initial mercury concentration of 30 μg/L and pH levels of both 3 and 5, a Mn dosage of 4 mg/L was able to lower the mercury concentration to meet the standards for drinking water quality at less than 1 μg/L. Analysis by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy suggests that the hydroxyls on the surface of Mn (hydr)oxides are the active sites for adsorption of trace mercury from aqueous solution.

The efficiency of macroporous polystyrene ion-exchange resins in natural organic matter removal from surface water

Directory of Open Access Journals (Sweden)

Urbanowska Agnieszka

2017-01-01

Full Text Available Natural water sources used for water treatment contains various organic and inorganic compounds. Surface waters are commonly contaminated with natural organic matter (NOM. NOM removal from water is important e.g. due to lowering the risk of disinfection by-product formation during chlorination. Ion exchange with the use of synthetic ion-exchange resins is an alternative process to typical NOM removal approach (e.g. coagulation, adsorption or oxidation as most NOM compounds have anionic character. Moreover, neutral fraction could be removed from water due to its adsorption on resin surface. In this study, applicability of two macroporous, polystyrene ion exchange resins (BD400FD and A100 in NOM removal from water was assessed including comparison of treatment efficiency in various process set-ups and conditions. Moreover, resin regeneration effectivity was determined. Obtained results shown that examined resins could be applied in NOM removal and it should be noticed that column set-up yielded better results (contrary to batch set-up. Among the examined resins A100 one possessed better properties. It was determined that increase of solution pH resulted in a slight decrease in treatment efficiency while higher temperature improved it. It was also observed that regeneration efficiency was comparable in both tested methods but batch set-up required less reagents.

Comparative efficiency of final endodontic cleansing procedures in removing a radioactive albumin from root canal systems

International Nuclear Information System (INIS)

Cecic, P.A.; Peters, D.D.; Grower, M.F.

1984-01-01

Fifty-six teeth were initially instrumented, with the use of seven irrigants or irrigant combinations, and filled with radioactive albumin. The study then showed the relative ability of three final endodontic procedures (copious reirrigation with saline solution, drying with paper points, and reassuring patency of the canal with the final instrument) to remove the albumin. Even after copious irrigation, each additional procedure removed statistically significant amounts of albumin. Alternating an organic solvent and an inorganic solvent did appear to leave the canal system in the optimal condition for final cleansing procedures. The study then correlated the relative efficiency of irrigation alone versus instrumentation plus irrigation in removing the remaining albumin from the canal systems. Reinstrumentation plus copious irrigation removed significantly more albumin than copious irrigation alone

Removal of 4-Chlorophenol from Aqueous Solutions Using Graphene Oxide Nanoporous Adsorbent

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akbar eslami

2015-03-01

Full Text Available In this study, graphene oxide was used as a nanostructured adsorbent with properties supposedly better than other common adsorbents to remove 4-chlorophenol from aqueous solutions. For this purpose, graphene oxide was initially synthesized using the Hummer's method and x-ray diffraction and scanning electron microscopy were employed to identify its morphology and structure. The variables involved in the absorption process (including 4-chlorophenol initial concentration, adsorbent dosage, and pH were investigated based on the one-factor-at-a-time method. Eventually, the data were confirmed against the Langmuir and Freundlich isotherms. It was found that the adsorption process reached equilibrium in 20 minutes. A dosage of 0.4 g/L graphene oxide at pH=8 brought about 90% removal of 10 mg/L 4-chlorophenol within 5 minutes. The adsorption isotherm was described well by the Langmuir isotherm model and the values for R2 and RL were recorded as 0.99 for and 0.34, respectively. Being a low cost and highly efficient process, the adsorption process using graphene oxide adsorbent may be recommended for the reduction and elimination of pollutants in the environment, especially those in aqueous solutions.

Experimental study of iodine removal efficiency in self-priming venturi scrubber

International Nuclear Information System (INIS)

Gulhane, N.P.; Landge, A.D.; Shukla, D.S.; Kale, S.S.

2015-01-01

Highlights: • Fabrication, erection of experimental set up and carrying out experimentation with self priming venturi scrubber. • Predicting solubility of iodine in water and its pH dependency. • Increasing pH of water increases iodine removal efficiency. • Maximum iodine removal efficiency is obtained at 10 pH of water using sodium thiosulphate. - Abstract: The objective of present experimental study is to examine the iodine removal efficiency of a self-priming venturi scrubber for submerged operating condition. The venturi scrubber is used in Containment Filtered Venting System of nuclear power plants to remove the gaseous pollutants from contaminated gas during severe accidents. The experiment consists of mixing the iodine vapours with the air using suction venturi and pressure cooker system. The purpose of iodine mixing with air is to examine scrubbing performance of the designed venturi scrubber with water as scrubbing liquid. The performance parameters of venturi scrubber are expressed mainly in terms of pressure drop and iodine removal efficiency. The iodine removal efficiency of venturi scrubber is estimated for a series of two experiments by measuring the quantity of iodine in water from iodometric titration with four distinct pH of water. It has been experimentally observed that iodine removal efficiency is improved by using higher pH value of scrubbing liquid since solubility of iodine gets improved at higher pH

The investigation of parameters affecting boron removal by electrocoagulation method

Energy Technology Data Exchange (ETDEWEB)

Yilmaz, A. Erdem [Department of Environmental Engineering, Atatuerk University, Faculty of Engineering, Erzurum (Turkey)]. E-mail: aerdemy@atauni.edu.tr; Boncukcuoglu, Recep [Department of Environmental Engineering, Atatuerk University, Faculty of Engineering, Erzurum (Turkey); Kocakerim, M. Muhtar [Department of Chemical Engineering, 25240, Atatuerk University, Faculty of Engineering Erzurum (Turkey); Keskinler, Buelent [Department of Environmental Engineering, Gebze Institute of Technology, Gebze/Kocaeli 41400 (Turkey)

2005-10-17

Boron removal from wastewaters by electrocoagulation using aluminum electrode material was investigated in this paper. Several working parameters, such as pH, current density, boron concentration and type and concentration of supporting electrolyte were studied in an attempt to achieve a higher removal capacity. The experiments were carried out by keeping the pH of solution constant and optimum pH of solution was determined 8.0 for the aluminum electrode. Although energy consumption increased with decreasing boron concentration, which conductivity of these solutions were low, boron removal efficiency was higher at 100 mg/L than that of 1000 mg/L. Current density was an important parameter affecting removal efficiency. Boron removal efficiency and energy consumption increased with increasing current density from 1.2 to 6.0 mA/cm{sup 2}. The types of different supporting electrolyte were experimented in order to investigate to this parameter effect on boron removal. The highest boron removal efficiency, 97%, was found by CaCl{sub 2}. Added CaCl{sub 2} increased more the conductivity of solution according to other supporting electrolytes, but decreased energy consumption. The results showed to have a high effectiveness of the electrocoagulation method in removing boron from aqueous solutions.

REMOVAL OF TRICHLOROACETIC ACID FROM THE AQUEOUS SOLUTIONS USING NATURAL AND ACTIVATED LIGNITE COALS

Directory of Open Access Journals (Sweden)

Hüseyin GÜLENSOY

1998-02-01

Full Text Available In these studies, a typical lignite coal found near Istanbul (Yeniköy and its activated products were used to adsorb TCA from aqueous solutions. Particle sizes of coal samples and the concentrations of TCA solutions were chosen as parameters against the fixed amount of adsorbent. The maximum efficiency has been obtained for the coal having (-120 + 150 mesh size fraction activated by heating. As a result, it was shown that these kinds of lignite coals could be used as a good adsorbent. In addition, it was also proved that both the removal and recovery of TCA from some waste waters would easily be possible.

Chromium (Ⅵ) removal from aqueous solutions through powdered activated carbon countercurrent two-stage adsorption.

Science.gov (United States)

Wang, Wenqiang

2018-01-01

To exploit the adsorption capacity of commercial powdered activated carbon (PAC) and to improve the efficiency of Cr(VI) removal from aqueous solutions, the adsorption of Cr(VI) by commercial PAC and the countercurrent two-stage adsorption (CTA) process was investigated. Different adsorption kinetics models and isotherms were compared, and the pseudo-second-order model and the Langmuir and Freundlich models fit the experimental data well. The Cr(VI) removal efficiency was >80% and was improved by 37% through the CTA process compared with the conventional single-stage adsorption process when the initial Cr(VI) concentration was 50 mg/L with a PAC dose of 1.250 g/L and a pH of 3. A calculation method for calculating the effluent Cr(VI) concentration and the PAC dose was developed for the CTA process, and the validity of the method was confirmed by a deviation of <5%. Copyright © 2017. Published by Elsevier Ltd.

An efficient algorithm for removal of inactive blocks in reservoir simulation

Energy Technology Data Exchange (ETDEWEB)

Abou-Kassem, J.H.; Ertekin, T. (Pennsylvania State Univ., PA (United States))

1992-02-01

In the efficient simulation of reservoirs having irregular boundaries one is confronted with two problems: the removal of inactive blocks at the matrix level and the development and application of a variable band-width solver. A simple algorithm is presented that provides effective solutions to these two problems. The algorithm is demonstrated for both the natural ordering and D4 ordering schemes. It can be easily incorporated in existing simulators and results in significant savings in CPU and matrix storage requirements. The removal of the inactive blocks at the matrix level plays a major role in effecting these savings whereas the application of a variable band-width solver plays an enhancing role only. The value of this algorithm lies in the fact that it takes advantage of irregular reservoir boundaries that are invariably encountered in almost all practical applications of reservoir simulation. 11 refs., 3 figs., 3 tabs.

Magnetic biochar combining adsorption and separation recycle for removal of chromium in aqueous solution.

Science.gov (United States)

Xin, Ouyang; Yitong, Han; Xi, Cao; Jiawei, Chen

2017-03-01

Biochar has been developed in recent years for the removal of contaminants such as Cr (VI) in water. The enhancement of the adsorption capacity of biochar and its recyclable use are still challenges. In this study, magnetic biochar derived from corncobs and peanut hulls was synthesized under different pyrolysis temperatures after pretreating the biomass with a low concentration of 0.5 M FeCl 3 solution. The morphology, specific surface area, saturation magnetization and Fourier transform infrared spectroscopy (FT-IR) spectra were characterized for biochar. The magnetic biochar performed well in combining adsorption and separation recycle for the removal of Cr (VI) in water. The Cr (VI) adsorbance of the biochar was increased with the increase in pyrolysis temperature, and the magnetic biochar derived from corncobs showed better performance for both magnetization and removal of Cr (VI) than that from peanut hulls. The Langmuir model was used for the isothermal adsorption and the maximum Cr (VI) adsorption capacity of corncob magnetic biochar pyrolyzed at 650 °C reached 61.97 mg/g. An alkaline solution (0.1 M NaOH) favored the desorption of Cr (VI) from the magnetic biochar, and the removal of Cr (VI) still remained around 77.6% after four cycles of adsorption-desorption. The results showed that corncob derived magnetic biochar is a potentially efficient and recoverable adsorbent for remediation of heavy metals in water.

Effect of compost age and composition on the atrazine removal from solution

Science.gov (United States)

Tsui, L.; Roy, W.R.

2007-01-01

Compost samples from two composting facilities, the Urbana (Illinois) Landscape Recycling Center (ULRC) and Illinois State University (ISU), were selected to examine the effect of compost age on atrazine removal from solution. The ULRC samples were made from yard waste without an additional nitrogen source. The ISU samples were made from yard waste or sawdust with the addition of manure. The 6-month-old ULRC compost had the greater capacity to remove atrazine from solution, which we attributed to its greater organic carbon content. The addition of nitrate into ULRC compost could influence the extent of atrazine removal, but did not have a significant impact on atrazine removal when applied to ISU compost, probably because manure was added to the yard waste to produce the compost. For both ULRC and ISU samples, the presence of sodium azide inhibited atrazine removal, suggesting that microbial activity contributed to the atrazine removal. Metabolic analysis demonstrated that hydroxyatrazine was the major identified metabolite that accumulated in solution before significant ring mineralization could occur. When compared with the ISU compost, the ULRC compost sample had a greater capacity to remove atrazine from solution during the 120 days of study because of the larger humic acid content. The experimental results suggested that less-mature compost may be better suited for environmental applications such as removing atrazine from tile-drainage waters. ?? 2006 Elsevier B.V. All rights reserved.

Effect of compost age and composition on the atrazine removal from solution.

Science.gov (United States)

Tsui, Lo; Roy, William R

2007-01-02

Compost samples from two composting facilities, the Urbana (Illinois) Landscape Recycling Center (ULRC) and Illinois State University (ISU), were selected to examine the effect of compost age on atrazine removal from solution. The ULRC samples were made from yard waste without an additional nitrogen source. The ISU samples were made from yard waste or sawdust with the addition of manure. The 6-month-old ULRC compost had the greater capacity to remove atrazine from solution, which we attributed to its greater organic carbon content. The addition of nitrate into ULRC compost could influence the extent of atrazine removal, but did not have a significant impact on atrazine removal when applied to ISU compost, probably because manure was added to the yard waste to produce the compost. For both ULRC and ISU samples, the presence of sodium azide inhibited atrazine removal, suggesting that microbial activity contributed to the atrazine removal. Metabolic analysis demonstrated that hydroxyatrazine was the major identified metabolite that accumulated in solution before significant ring mineralization could occur. When compared with the ISU compost, the ULRC compost sample had a greater capacity to remove atrazine from solution during the 120 days of study because of the larger humic acid content. The experimental results suggested that less-mature compost may be better suited for environmental applications such as removing atrazine from tile-drainage waters.

Efficient adsorptive removal of Congo red from aqueous solution by synthesized zeolitic imidazolate framework-8

Directory of Open Access Journals (Sweden)

Canlan Jiang

2016-10-01

Full Text Available Dyes exposure in aquatic environment creates risks to human health and biota due to their intrinsic toxic mutagenic and carcinogenic characteristics. In this work, a metal-organic frameworks materials, zeolitic imidazolate framework-8 (ZIF-8, was synthesized through hydrothermal reaction for the adsorptive removal of harmful Congo red (CR from aqueous solution. Results showed that the maximum adsorption capacity of CR onto ZIF-8 was ultrahigh as 1250 mg g−1. Adsorption behaviors can be successfully fitted by the pseudo-second order kinetic model and the Langmuir isotherm equation. Solution conditions (pH condition and the co-exist anions may influent the adsorption behaviors. The adsorption performance at various temperatures indicated the process was a spontaneous and endothermic adsorption reaction. The enhanced adsorption capacity was determined due to large surface area of ZIF-8 and the strong interactions between surface groups of ZIF-8 and CR molecules including the electrostatic interaction between external active sites Zn−OH on ZIF-8 -and −SO3 or –N=N– sites in CR molecule, and the π–π interaction.

Efficient removal of malachite green dye using biodegradable graft copolymer derived from amylopectin and poly(acrylic acid).

Science.gov (United States)

Sarkar, Amit Kumar; Pal, Aniruddha; Ghorai, Soumitra; Mandre, N R; Pal, Sagar

2014-10-13

This article reports on the application of a high performance biodegradable adsorbent based on amylopectin and poly(acrylic acid) (AP-g-PAA) for removal of toxic malachite green dye (MG) from aqueous solution. The graft copolymer has been synthesized and characterized using various techniques including FTIR, GPC, SEM and XRD analyses. Biodegradation study suggests that the co-polymer is biodegradable in nature. The adsorbent shows excellent potential (Qmax, 352.11 mg g(-1); 99.05% of MG has been removed within 30 min) for removal of MG from aqueous solution. It has been observed that point to zero charge (pzc) of graft copolymer plays significant role in adsorption efficacy. The adsorption kinetics and isotherm follow pseudo-second order and Langmuir isotherm models, respectively. Thermodynamics parameters suggest that the process of dye uptake is spontaneous. Finally desorption study shows excellent regeneration efficiency of adsorbent. Copyright © 2014 Elsevier Ltd. All rights reserved.

Arsenic removal from alkaline leaching solution using Fe (III) precipitation.

Science.gov (United States)

Wang, Yongliang; Lv, Cuicui; Xiao, Li; Fu, Guoyan; Liu, Ya; Ye, Shufeng; Chen, Yunfa

2018-02-02

The alkaline leaching solution from arsenic-containing gold concentrate contains a large amount of arsenate ions, which should be removed because it is harmful to the production process and to the environment. In this study, conventional Fe (III) precipitation was used to remove arsenic from the leaching solution. The precipitation reaction was carried out at the normal temperature, and the effects of pH value and Fe/As ratio on the arsenic removal were investigated. The results show that the removal rate of arsenic is distinctive at different pH values, and the effect is best within the pH range of 5.25-5.96. The removal rate can be further increased by increasing the ratio of Fe/As. When the pH = 5.25-5.96 and Fe/As > 1.8, the arsenic in the solution can be reduced to below 5 mg/L. However, the crystallinity of ferric arsenate is poor, and the particle size is small, most of which is about 1 μm. The leaching toxicity test shows the leaching toxicity of precipitates gradually decreased by the increase of Fe/As. The precipitates can be stored safely as the ratio of Fe/As exceeded 2.5.

Persimmon leaf bio-waste for adsorptive removal of heavy metals from aqueous solution.

Science.gov (United States)

Lee, Seo-Yun; Choi, Hee-Jeong

2018-03-01

The aim of this study was to investigate heavy metal removal using waste biomass adsorbent, persimmon leaves, in an aqueous solution. Persimmon leaves, which are biomaterials, have a large number of hydroxyl groups and are highly suitable for removal of heavy metals. Therefore, in this study, we investigated the possibility of removal of Cu, Pb, and Cd in aqueous solution by using raw persimmon leaves (RPL) and dried persimmon leaves (DPL). Removal of heavy metals by RPL and DPL showed that DPL had a 10%-15% higher removal than RPL, and the order of removal efficiency was found to be Pb > Cu > Cd. The pseudo-second order model was a better fit to the heavy metal adsorption experiments using RPL and DPL than the pseudo-first order model. The adsorption of Cu, Pb, and Cd by DPL was more suitable with the Freundlich isothermal adsorption and showed an ion exchange reaction which occurred in the uneven adsorption surface layer. The maximum adsorption capacity of Cu, Pb, and Cd was determined to be 19.42 mg/g, 22.59 mg/g, and 18.26 mg/g, respectively. The result of the adsorption experiments showed that the n value was higher than 2 regardless of the dose, indicating that the heavy metal adsorption on DPL was easy. In the thermodynamic experiment, ΔG° was a negative value, and ΔH° and ΔS° were positive values. It can be seen that the heavy metal adsorption process using DPL was spontaneous in nature and was an endothermic process. Moreover, as the temperature increased, the adsorption increased, and the affinity of heavy metal adsorption to DPL was very good. This experiment, in which heavy metals are removed using the waste biomass of persimmon leaves is an eco-friendly new bioadsorbent method because it can remove heavy metals without using chemicals while utilizing waste recycling. Copyright © 2018 Elsevier Ltd. All rights reserved.

Eggshell Powder as an Adsorbent for Removal of Fluoride from Aqueous Solution: Equilibrium, Kinetic and Thermodynamic Studies

Directory of Open Access Journals (Sweden)

R. Bhaumik

2012-01-01

Full Text Available A new medium, eggshell powder has been developed for fluoride removal from aqueous solution. Fluoride adsorption was studied in a batch system where adsorption was found to be pH dependent with maximum removal efficiency at 6.0. The experimental data was more satisfactorily fitted with Langmuir isotherm model. The kinetics and the factor controlling adsorption process fully accepted by pseudo-second-order model were also discussed. Ea was found to be 45.98 kJmol-1 by using Arrhenius equation, indicating chemisorption nature of fluoride onto eggshell powder. Thermodynamic study showed spontaneous nature and feasibility of the adsorption process with negative enthalpy (∆H0 value also supported the exothermic nature. Batch experiments were performed to study the applicability of the adsorbent by using fluoride contaminated water collected from affected areas. These results indicate that eggshell powder can be used as an effective, low-cost adsorbent to remove fluoride from aqueous solution as well as groundwater.

Adsorptive removal of arsenate from aqueous solutions by biochar supported zero-valent iron nanocomposite: Batch and continuous flow tests

International Nuclear Information System (INIS)

Wang, Shengsen; Gao, Bin; Li, Yuncong; Creamer, Anne Elise; He, Feng

2017-01-01

Highlights: • Biochar supported nZVI (nZVI/BC) was synthesized. • nZVI/BC showed excellent As(V) removal efficiency in batch and CMR experiments. • 100% removal efficiency was achieved in CMRs. • Surface adsorption was the dominant removal mechanism. - Abstract: Arsenate (As(V)) removal ability by nanoscale zero-valent iron (nZVI) is compromised by aggregation of nZVI particles. In this work, pine derived biochar (PB) was used as a supporting material to stabilize nZVI for As(V) removal. The biochar supported nZVI (nZVI/BC) was synthesized by precipitating the nanoparticles on carbon surfaces. Experiments using batch and continuous flow, completely mixed reactors (CMRs) were carried out to investigate the removal of As(V) by the nZVI/BC from aqueous solutions. Batch experiments showed that nZVI/BC had high As(V) removal capacity in a wide range of pH (3–8). Kinetic data revealed that equilibrium was reached within 1 h and the isotherm data showed that the Langmuir maximum adsorption capacity of the nZVI/BC for As(V) at pH 4.1 was 124.5 g kg −1 . As(V) (100 mg L −1 ) adsorption in anoxic condition was about 8% more than in oxic conditions, where As(V) reduction was observed in anoxic condition. The performance of the nZVI/BC in flowing condition was evaluated in CMRs at influent As(V) concentrations of 2.1 and 5.5 mg L −1 and the adsorbent removed 100% and 90% of the As(V), respectively. Furthermore, the nZVI/BC composite is magnetic which facilitates collection from aqueous solutions.

Adsorptive removal of arsenate from aqueous solutions by biochar supported zero-valent iron nanocomposite: Batch and continuous flow tests

Energy Technology Data Exchange (ETDEWEB)

Wang, Shengsen [Department of Agricultural and Biological Engineering, University of Florida, Gainesville, FL 32611 (United States); Gao, Bin, E-mail: bg55@ufl.edu [Department of Agricultural and Biological Engineering, University of Florida, Gainesville, FL 32611 (United States); Li, Yuncong [Tropical Research and Education Center, University of Florida, Homestead, FL 33031 (United States); Creamer, Anne Elise [Department of Agricultural and Biological Engineering, University of Florida, Gainesville, FL 32611 (United States); He, Feng [College of Biological and Environmental Engineering, Zhejiang University of Technology, Hangzhou, Zhejiang 310014 (China)

2017-01-15

Highlights: • Biochar supported nZVI (nZVI/BC) was synthesized. • nZVI/BC showed excellent As(V) removal efficiency in batch and CMR experiments. • 100% removal efficiency was achieved in CMRs. • Surface adsorption was the dominant removal mechanism. - Abstract: Arsenate (As(V)) removal ability by nanoscale zero-valent iron (nZVI) is compromised by aggregation of nZVI particles. In this work, pine derived biochar (PB) was used as a supporting material to stabilize nZVI for As(V) removal. The biochar supported nZVI (nZVI/BC) was synthesized by precipitating the nanoparticles on carbon surfaces. Experiments using batch and continuous flow, completely mixed reactors (CMRs) were carried out to investigate the removal of As(V) by the nZVI/BC from aqueous solutions. Batch experiments showed that nZVI/BC had high As(V) removal capacity in a wide range of pH (3–8). Kinetic data revealed that equilibrium was reached within 1 h and the isotherm data showed that the Langmuir maximum adsorption capacity of the nZVI/BC for As(V) at pH 4.1 was 124.5 g kg{sup −1}. As(V) (100 mg L{sup −1}) adsorption in anoxic condition was about 8% more than in oxic conditions, where As(V) reduction was observed in anoxic condition. The performance of the nZVI/BC in flowing condition was evaluated in CMRs at influent As(V) concentrations of 2.1 and 5.5 mg L{sup −1} and the adsorbent removed 100% and 90% of the As(V), respectively. Furthermore, the nZVI/BC composite is magnetic which facilitates collection from aqueous solutions.

Nanotubular Halloysite Clay as Efficient Water Filtration System for Removal of Cationic and Anionic Dyes

International Nuclear Information System (INIS)

Zhao, Yafei; Abdullayev, Elshad; Lvov, Yuri

2014-01-01

Halloysite nanotubes, chemically similar to kaolinite, are formed by rolling of kaolinite layers in tubes with diameter of 50 nm and length of ca. 1 μm. Halloysite has negative SiO 2 outermost and positive Al 2 O 3 inner lumen surface, which enables it to be used as potential absorbent for both cationic and anionic dyes due to the efficient bivalent adsorbancy. An adsorption study using cationic Rhodamine 6G and anionic Chrome azurol S has shown approximately two times better dye removal for halloysite as compared to kaolinite. Halloysite filters have been effectively regenerated up to 50 times by burning the adsorbed dyes. Overall removal efficiency of anionic Chrome azurol S exceeded 99.9% for 5th regeneration cycle of halloysite. Chrome azurol S adsorption capacity decreases with the increase of ionic strength, temperature and pH. For cationic Rhodamine 6G, higher ionic strength, temperature and initial solution concentration were favorable to enhanced adsorption with optimal pH 8. These results indicate a potential to utilize halloysite for the removal of ionic dyes from environmental waters

Removal of radium from aqueous sulphate solutions

International Nuclear Information System (INIS)

Weir, D.R.; Masters, J.T.; Neven, M.

1983-01-01

Radium is often present in ores and an aqueous solution associated with the ore may consequently contain dissolved radium. It is frequently necessary to remove radium from such solutions to reduce the total radium content to a prescribed low level before the solution can be returned to the environment. The present invention is based on the discovery that the total radium content can be reduced to a satisfactory level within a reasonable time by adding a soluble barium salt to a radium-containing sulphate solution which also contains dissolved magnesium at a pH not greater than about 0 to precipitate radium as barium radium sulphate, raising the pH to at least 11 to precipitate an insoluble magnesium compound which collects the barium radium sulphate precipitate, and separating substantially all of the precipitates from the solution

Ion exchange removal of technetium from salt solutions

International Nuclear Information System (INIS)

Walker, D.D.

1983-01-01

Ion exchange methods for removing technetium from waste salt solutions have been investigated by the Savannah River Laboratory (SRL). These experiments have shown: Commercially available anion exchange resins show high selectivity and capacity for technetium. In column runs, 150 column volumes of salt solution were passed through an ion exchange column before 50% 99 Tc breakthrough was reached. The technetium can be eluted from the resin with nitric acid. Reducing resins (containing borohydride) work well in simple hydroxide solutions, but not in simulated salt solutions. A mercarbide resin showed a very high selectivity for Tc, but did not work well in column operation

Efficient Removal of Cationic and Anionic Radioactive Pollutants from Water Using Hydrotalcite-Based Getters.

Science.gov (United States)

Bo, Arixin; Sarina, Sarina; Liu, Hongwei; Zheng, Zhanfeng; Xiao, Qi; Gu, Yuantong; Ayoko, Godwin A; Zhu, Huaiyong

2016-06-29

Hydrotalcite (HT)-based materials are usually applied to capture anionic pollutants in aqueous solutions. Generally considered anion exchangers, their ability to capture radioactive cations is rarely exploited. In the present work, we explored the ability of pristine and calcined HT getters to effectively capture radioactive cations (Sr(2+) and Ba(2+)) which can be securely stabilized at the getter surface. It is found that calcined HT outperforms its pristine counterpart in cation removal ability. Meanwhile, a novel anion removal mechanism targeting radioactive I(-) is demonstrated. This approach involves HT surface modification with silver species, namely, Ag2CO3 nanoparticles, which can attach firmly on HT surface by forming coherent interface. This HT-based anion getter can be further used to capture I(-) in aqueous solution. The observed I(-) uptake mechanism is distinctly different from the widely reported ion exchange mechanism of HT and much more efficient. As a result of the high local concentrations of precipitants on the getters, radioactive ions in water can be readily immobilized onto the getter surface by forming precipitates. The secured ionic pollutants can be subsequently removed from water by filtration or sedimentation for safe disposal. Overall, these stable, inexpensive getters are the materials of choice for removal of trace ionic pollutants from bulk radioactive liquids, especially during episodic environmental crisis.

Heavy metal removal from aqueous solutions by sorption using ...

African Journals Online (AJOL)

Heavy metal removal from aqueous solutions by sorption using natural clays from Burkina Faso. ... The high alkaline pH in one of the samples is attributable to the presence of ... The point of zero charge (pHpzc) values of the clays, as determined by ... significant contributions to the removal of metal ions in aqueous systems.

Efficiency of lipopeptide biosurfactants in removal of petroleum hydrocarbons and heavy metals from contaminated soil.

Science.gov (United States)

Singh, Anil Kumar; Cameotra, Swaranjit Singh

2013-10-01

This study describes the potential application of lipopeptide biosurfactants in removal of petroleum hydrocarbons and heavy metals from the soil samples collected from industrial dumping site. High concentrations of heavy metals (like iron, lead, nickel, cadmium, copper, cobalt and zinc) and petroleum hydrocarbons were present in the contaminated soil samples. Lipopeptide biosurfactant, consisting of surfactin and fengycin was obtained from Bacillus subtilis A21. Soil washing with biosurfactant solution removed significant amount of petroleum hydrocarbon (64.5 %) and metals namely cadmium (44.2 %), cobalt (35.4 %), lead (40.3 %), nickel (32.2 %), copper (26.2 %) and zinc (32.07 %). Parameters like surfactant concentration, temperature, agitation condition and pH of the washing solution influenced the pollutant removing ability of biosurfactant mixture. Biosurfactant exhibited substantial hydrocarbon solubility above its critical micelle concentration. During washing, 50 % of biosurfactant was sorbed to the soil particles decreasing effective concentration during washing process. Biosurfactant washed soil exhibited 100 % mustard seed germination contradictory to water washed soil where no germination was observed. The results indicate that the soil washing with mixture of lipopeptide biosurfactants at concentrations above its critical micelle concentration can be an efficient and environment friendly approach for removing pollutants (petroleum hydrocarbon and heavy metals) from contaminated soil.

Removal mechanism of phosphate from aqueous solution by fly ash.

Science.gov (United States)

Lu, S G; Bai, S Q; Zhu, L; Shan, H D

2009-01-15

This work studied the effectiveness of fly ash in removing phosphate from aqueous solution and its related removal mechanism. The adsorption and precipitation of phosphate by fly ash were investigated separately in order to evaluate their role in the removal of phosphate. Results showed that the removal of phosphate by fly ash was rapid. The removal percentage of phosphate in the first 5min reached 68-96% of the maximum removal of phosphate by fly ash. The removal processes of phosphate by fly ash included a fast and large removal representing precipitation, then a slower and longer removal due to adsorption. The adsorption of phosphate on fly ash could be described well by Freundlich isotherm equation. The pH and Ca2+ concentration of fly ash suspension were decreased with the addition of phosphate, which suggests that calcium phosphate precipitation is a major mechanism of the phosphate removal. Comparison of the relative contribution of the adsorption and precipitation to the total removal of phosphate by fly ash showed that the adsorption accounted for 30-34% of the total removal of phosphate, depending on the content of CaO in fly ash. XRD patterns of the fly ash before and after phosphate adsorption revealed that phosphate salt (CaHPO4 x 2H2O) was formed in the adsorption process. Therefore, the removal of phosphate by fly ash can be attributed to the formation of phosphate precipitation as a brushite and the adsorption on hydroxylated oxides. The results suggested that the use of fly ash could be a promising solution to the removal of phosphate in the wastewater treatment and pollution control.

Efficiency of Aluminum and Iron Electrodes for the Removal of Heavy Metals [(Ni (II), Pb (II), Cd (II)] by Electrocoagulation Method

Energy Technology Data Exchange (ETDEWEB)

Khosa, Muhammad Kaleem; Jamal, Muhammad Asghar; Hussain, Amira; Muneer, Majid; Zia, Khalid Mahmood [Government College Univ., Faisalabad (Pakistan); Hafeez, Samia [Bahaud-din-Zakariya Univ., Multan (Pakistan)

2013-06-15

Electrocoagulation (EC) technique is applied for the treatment of wastewater containing heavy metals ions such as nickel (Ni), lead (Pb) and cadmium (Cd) by using sacrificial anodes corrode to release active coagulant flocs usually aluminium or iron cations into the solution. During electrolytic reactions hydrogen gas evolve at the cathode. All the experiments were carried out in Batch mode. The tank was filled with synthetic wastewater containing heavy metals and efficiency of electrocoagulation in combination with aluminum and iron electrodes were investigated for removal of such metals. Several parameters, such as contact time, pH, electro-coagulant concentration, and current density were optimized to achieve maximum removal efficiency (%). The concentrations of heavy metals were determined by using Atomic Absorption Spectroscopy (AAS). It is found that the electro-coagulation process has potential to be utilized for the cost-effective removal of heavy metals from wastewater specially using iron electrodes in terms of high removal efficiencies and operating cost.

Efficiency of Aluminum and Iron Electrodes for the Removal of Heavy Metals [(Ni (II), Pb (II), Cd (II)] by Electrocoagulation Method

International Nuclear Information System (INIS)

Khosa, Muhammad Kaleem; Jamal, Muhammad Asghar; Hussain, Amira; Muneer, Majid; Zia, Khalid Mahmood; Hafeez, Samia

2013-01-01

Electrocoagulation (EC) technique is applied for the treatment of wastewater containing heavy metals ions such as nickel (Ni), lead (Pb) and cadmium (Cd) by using sacrificial anodes corrode to release active coagulant flocs usually aluminium or iron cations into the solution. During electrolytic reactions hydrogen gas evolve at the cathode. All the experiments were carried out in Batch mode. The tank was filled with synthetic wastewater containing heavy metals and efficiency of electrocoagulation in combination with aluminum and iron electrodes were investigated for removal of such metals. Several parameters, such as contact time, pH, electro-coagulant concentration, and current density were optimized to achieve maximum removal efficiency (%). The concentrations of heavy metals were determined by using Atomic Absorption Spectroscopy (AAS). It is found that the electro-coagulation process has potential to be utilized for the cost-effective removal of heavy metals from wastewater specially using iron electrodes in terms of high removal efficiencies and operating cost

Removal of heavy metals from sludge of Sanaru-Lake by electrokinetics

Energy Technology Data Exchange (ETDEWEB)

Seno, T.; Shiba, S.; Hirata, Y. [Dept. of Systems Engineering, Shizuoka Univ., Hamamatsu (Japan)

2001-07-01

Two kinds of experiments were carried out for the removal of heavy metals from soils by electrokinetic technique. One was the removal of lead from kaolinite by using a small-sized test cell. The effect of the kind of purging solutions (such as distilled water, tap water, acetic acid and nitric acid) on removal efficiency was examined. High removal efficiency was obtained for the acetic acid solution. It was found that the controlling pH of solution surrounding cathode had a significant influence on the removal efficiency. The other experiment was the removal of heavy metals from the bottom sludge of Sanaru Lake. Zinc, nickel and copper in the sludge were successfully removed, but lead and chromium were hardly able to remove from the sludge. The simplified one-dimensional mathematical model was proposed. The prediction by the model was qualitatively agreed with the experimental result. (orig.)

Assessment of Cadmium (II) and Chromium (VI) removal from aqueous solution using coconut “Cocosnucifera” Coir as biosorbent in batch and fixed-bed column adsorption

International Nuclear Information System (INIS)

Capili, M.L.S.; Escover, J.J.; San Miguel, J.A.N.; Duavis, A.G.; Sucgang, R.J.

2015-01-01

Heavy metals from industrial effluents are considered contaminants and pose various health risks. Coconut coir is an agricultural waste material abundantly found in the Philippines and is a potential biosorbent of heavy metals. The adsorption of cadmium (II) and chromium (VI) in aqueous solutions were studied under different parameters using coconut coir as the adsorbent. The properties of coconut coir such as crystalline and morphological structure, along with the functional groups present were determined using XRD, SEM and FTIR respectively. The effect of solution pH, initial metal ion concentration and adsorbent dose were determined and optimized concentration of each solution was carried out using AAS. XRF was done to prove that the decrease of metal concentration in the solution was due to the adsorption of the coir. The data obtained from the optimum parameter of each metal were fitted to the Freundlich and Langmuir isotherm models as well as Elovich, first-order and second-order Lagergren kinetic models. These parameters were also used for the adsorption column experiment to determine and compare the adsorption capacity of the coir when applied to a continuous process. Removal optimum parameters for cadmium were at pH 4, initial metal ion concentration of 0.2 mg/L and 0.6g adsorbent dose with a removal efficiency of 99.62%. Optimum parameters for chromium were obtained at pH 5, initial metal ion concentration of 1.2 mg/L and 1g adsorbent dose with a removal efficiency 10.52%. The study indicated that coconut coir is significantly effective in the adsorption of cadmium ions in aqueous solutions than chromium ions based on the reported removal efficiency.(author)

Removal of nitrate from aqueous solution using cetylpyridinium bromide (CPB) modified zeolite as adsorbent

International Nuclear Information System (INIS)

Zhan Yanhui; Lin Jianwei; Zhu Zhiliang

2011-01-01

Surfactant modified zeolites (SMZ) with different coverage types were prepared by loading the cetylpyridinium bromide (CPB) onto the surface of the natural zeolites. The adsorption behavior of nitrate on SMZ was investigated. Natural zeolite and SMZ with monolayer CPB coverage were inefficient for the removal of nitrate from aqueous solution. However, SMZ with patchy bilayer or bilayer CPB coverage was efficient in nitrate removal, and the nitrate adsorption capacity of SMZ increased with its CPB loading. For typical SMZ with bilayer CPB coverage, the nitrate adsorption process was well described by the pseudo-second-order kinetic model, and the experimental isotherm data fitted well with the Langmuir, Freundlich and Dubinin-Redushkevich isotherm models. Thermodynamic parameters such as Gibbs free energy change, enthalpy change and entropy change were calculated and the results showed that the adsorption of nitrate on SMZ was spontaneous and exothermic in nature. The presence of competing anions such as chloride, sulfate and bicarbonate ions slightly reduced the nitrate adsorption efficiency. Anionic exchange and electrostatic interaction were proven to be the main mechanisms that govern the adsorption of nitrate on SMZ.

Synthesis of Ce(III)-doped Fe{sub 3}O{sub 4} magnetic particles for efficient removal of antimony from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Qi, Zenglu; Joshi, Tista Prasai [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Liu, Ruiping, E-mail: liuruiping@rcees.ac.cn [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Liu, Huijuan [University of Chinese Academy of Sciences, Beijing 100049 (China); State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085 (China); Qu, Jiuhui [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China)

2017-05-05

Highlights: • Doping of Ce into Fe{sub 3}O{sub 4} was achieved based on a facile solvothermal method. • After doping, the removal capacity was increased by 5 times for “Sb(V)” and 2 times for “Sb(III)”. • Decreasing pH improved adsorption of Sb(V) but decreased adsorption of Sb(III). • Antimony sorption mechanisms on Ce-doped Fe{sub 3}O{sub 4} were illustrated. - Abstract: Aqueous antimony (Sb) pollution from human activity is of great concern in drinking water due to its adverse health effect. Magnetic Fe{sub 3}O{sub 4} particles, with high separation ability from solution, have been considered as a low-cost Sb adsorbent for contaminants. However, the limited adsorption capacity has restricted its practical application. In this study, a solvothermal approach was developed for doping Ce(III) into Fe{sub 3}O{sub 4}, thereby increasing the adsorption efficacy for both Sb(III) and Sb(V). In contrast to un-doped Fe{sub 3}O{sub 4}, the adsorption capacity towards Sb(III) and Sb(V) in Ce-doped materials increased from 111.4 to 224.2 mg/g and from 37.2 to 188.1 mg/g at neutral pH, respectively. Based on the combined results of XPS, XRD, and FTIR, it confirmed that Ce atom successfully doped into the Fe{sub 3}O{sub 4} structure, resulting in the decreased particle size, increased the surface area, and isoelectric point. Furthermore, the vibrating sample magnetometer (VSM) results showed that the Ce doping process had some side effects on the primitive magnetic property, but remaining the high separation potential during water treatment. According to the high removal efficiency and magnetic property, the Ce-doped Fe{sub 3}O{sub 4} of great simplicity should be a promising adsorbent for aqueous Sb removal.

Removal of Cr(VI) from aqueous solution by flocculant with the capacity of reduction and chelation

International Nuclear Information System (INIS)

Wang, Gang; Chang, Qing; Han, Xiaoting; Zhang, Mingyue

2013-01-01

Highlights: ► We report a novel flocculant with the properties of reduction and chelation for Cr. ► The removal of Cr(VI) by the flocculant depends highly on pH value. ► Some coexisting ions inhibit Cr (VI) removal, but promote total Cr removal. ► Cr and turbidity can be removed simultaneously in the treated wastewater. ► The interaction mechanism is investigated by FTIR and SEM. -- Abstract: A novel agent polyethyleneimine-sodium xanthogenate (PEX) with the multifunction of reduction, chelation, flocculation and precipitation was synthesized by using polyethyleneimine (PEI), carbon disulfide (CS 2 ), and sodium hydroxide (NaOH). The effects of different important parameters, such as pH value, initial Cr(VI) concentration, coexisting ions and turbidity etc., on the removal of chromium from aqueous solution by PEX were investigated in flocculation experiments. The experiments results demonstrated that PEX could efficiently remove Cr(VI) and total Cr (Cr(VI) + Cr(III)) in strongly acidic media. It was proved that the presence of coexisting ions (Na + , Ca 2+ , F − , Cl − , and SO 4 2− ) in the solution had a little influence on the removal of chromium. Furthermore, it was conformed that Cr(VI) ions and turbidity could be simultaneously removed when water samples contained both Cr(VI) ions and turbidity. Finally, the mechanism of interaction between chromium and PEX was further confirmed by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The results reveal that dithiocarboxylic acid groups on PEX macromolecule play a major role in Cr(VI) reduction and Cr(III) chelation, and the flocs formation is attributed to the interparticle bridging mechanism of PEX

Removal of Cadmium and Lead from Aqueous Solution by Hydroxyapatite/Chitosan Hybrid Fibrous Sorbent: Kinetics and Equilibrium Studies

Directory of Open Access Journals (Sweden)

Soyeon Park

2015-01-01

Full Text Available Hydroxyapatite (HAp/chitosan composites were prepared by a coprecipitation method, dropping a mixture of chitosan solution and phosphoric acid solution into a calcium hydroxide solution. Using the HAp/chitosan composites prepared, HAp/chitosan hybrid fibers with various HAp contents were prepared by a wet spinning method. X-ray diffraction and scanning electron microscopy analyses revealed that HAp particles were coated onto the surface of the fiber, and the surface roughness increased with increasing the HAp contents in the fiber. In order to evaluate the heavy metal removal characteristics of the HAp/chitosan hybrid fiber, adsorption tests were conducted and the results were compared with those of bare chitosan fibers. The results showed better performance in heavy metal ion removal for the HAp/chitosan hybrid fiber than the chitosan fiber. As the HAp content in the hybrid fiber increased, the removal efficiency of heavy metal ions also increased due to the increase of the specific surface area of the HAp/chitosan hybrid fiber. Adsorption kinetic and isotherm tests revealed that Pb2+ and Cd2+ adsorption to the hybrid fiber follows pseudo-second-order kinetic and Langmuir-type adsorption, respectively.

A comparative study of the removal of trivalent chromium from aqueous solutions by bentonite and expanded perlite

International Nuclear Information System (INIS)

Chakir, Achraf; Bessiere, Jacques; Kacemi, Kacem EL.; Marouf, Bouchaieb

2002-01-01

Local bentonite and expanded perlite (Morocco) have been characterised and used for the removal of trivalent chromium from aqueous solutions. The kinetic study had showed that the uptake of Cr(III) by bentonite is very rapid compared to expanded perlite. To calculate the sorption capacities of the two sorbents, at different pH, the experimental data points have been fitted to the Freundlich and Langmuir models, respectively, for bentonite and expanded perlite. For both sorbents the sorption capacity increases with increasing the pH of the suspensions. The removal efficiency has been calculated for both sorbents resulting that bentonite (96% of Cr(III) was removed) is more effective in removing trivalent chromium from aqueous solution than expanded perlite (40% of Cr(III) was removed). In the absence of Cr(III) ions, both bentonite and expanded perlite samples yield negative zeta potential in the pH range of 2-11. The changes of expanded perlite charge, from negative to positive, observed after contact with trivalent chromium(III) solutions was related to Cr(III) sorption on the surface of the solid. Thus, it was concluded that surface complexation plays an important role in the sorption of Cr(III) species on expanded perlite. In the case of bentonite, cation-exchange is the predominate mechanism for sorption of trivalent chromium ions, wherefore no net changes of zeta potential was observed after Cr(III) sorption. X-ray photoelectron spectroscopy measurements, at different pH values, were also made to corroborate the zeta potential results

Performance Evaluation of Ozonation Combined with Persulfate Application for Removal of Furfural from Aqueous Solutions

Directory of Open Access Journals (Sweden)

Alireza Rahmani

2017-03-01

Full Text Available Background: Furfural is an organic compound which derived from a variety industrial, including petrochemicals, pulping, pharmaceutical, food. Also is a main agent in many industries and aromatic organic compounds entrance in the environment. There are several methods of treating including physical, chemical, biological and physicochemical for remove this matter. Among advanced oxidation methods can be combined ozonation process with persulfate catalytic are noted. The purpose of this study was to evaluate the efficiency of ozonation process with the use of persulfate in removal furfural from aqueous solution. Materials and Methods: In this study, the efficiency of the process with a concentration furfural 5 to 30 mg/L, concentration persulfate 4 to 15 mM, pH = 3-11 and reaction time of 35 minutes in the semi-continuous reactor with a capacity of one liter was obtained. Results: The results of this study have been shown in  conditions of operation optimal , pH =,3 persulfate dosage 12 mM, ozone dosage of 1 g/min and the initial concentration of furfural  5 mg/L, this process is capable  remove of %93/34 percent Furfural and %70 of the initial COD. Conclusion: The results of this study showed that the ozone/persulfate process can be a suitable process for the removal of organic aromatic compounds including pollutants of interest.

Parallel artificial liquid membrane extraction as an efficient tool for removal of phospholipids from human plasma.

Science.gov (United States)

Ask, Kristine Skoglund; Bardakci, Turgay; Parmer, Marthe Petrine; Halvorsen, Trine Grønhaug; Øiestad, Elisabeth Leere; Pedersen-Bjergaard, Stig; Gjelstad, Astrid

2016-09-10

Generic Parallel Artificial Liquid Membrane Extraction (PALME) methods for non-polar basic and non-polar acidic drugs from human plasma were investigated with respect to phospholipid removal. In both cases, extractions in 96-well format were performed from plasma (125μL), through 4μL organic solvent used as supported liquid membranes (SLMs), and into 50μL aqueous acceptor solutions. The acceptor solutions were subsequently analysed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) using in-source fragmentation and monitoring the m/z 184→184 transition for investigation of phosphatidylcholines (PC), sphingomyelins (SM), and lysophosphatidylcholines (Lyso-PC). In both generic methods, no phospholipids were detected in the acceptor solutions. Thus, PALME appeared to be highly efficient for phospholipid removal. To further support this, qualitative (post-column infusion) and quantitative matrix effects were investigated with fluoxetine, fluvoxamine, and quetiapine as model analytes. No signs of matrix effects were observed. Finally, PALME was evaluated for the aforementioned drug substances, and data were in accordance with European Medicines Agency (EMA) guidelines. Copyright © 2016 Elsevier B.V. All rights reserved.

Silver removal from aqueous solution by biochar produced from biosolids via microwave pyrolysis.

Science.gov (United States)

Antunes, Elsa; Jacob, Mohan V; Brodie, Graham; Schneider, Philip A

2017-12-01

The contamination of water with silver has increased due to the widespread applications of products with silver employed as antimicrobial agent. Adsorption is a cost-effective method for silver removal from aqueous solution. In this study biochar, produced from the microwave assisted pyrolysis of biosolids, was used for silver removal from an aqueous solution. The adsorption kinetics, isotherms and thermodynamics were investigated to better understand the silver removal process by biochar. X-ray diffraction results demonstrated that silver removal was a combination two consecutive mechanisms, reduction and physical adsorption. The Langmuir model fitted the experimental data well, showing that silver removal was predominantly a surface mechanism. The thermodynamic investigation demonstrated that silver removal by biochar was an exothermic process. The final nanocomposite Ag-biochar (biochar plus silver) was used for methylene blue adsorption and photodegradation. This study showed the potential of using biochar produced from biosolids for silver removal as a promising solution to mitigate water pollution and an environmentally sustainable approach for biosolids management and re-use. Copyright © 2017 Elsevier Ltd. All rights reserved.

Optimization of Removal Efficiency and Minimum Contact Time for Cadmium and Zinc Removal onto Iron-modified Zeolite in a Two-stage Batch Sorption Reactor

Directory of Open Access Journals (Sweden)

M. Ugrina

2018-01-01

Full Text Available In highly congested industrial sites where significant volumes of effluents have to be treated in the minimum contact time, the application of a multi-stage batch reactor is suggested. To achieve better balance between capacity utilization and cost efficiency in design optimization, a two-stage batch reactor is usually the optimal solution. Thus, in this paper, a two-stage batch sorption design approach was applied to the experimental data of cadmium and zinc uptake onto iron-modified zeolite. The optimization approach involves the application of the Vermeulen’s approximation model and mass balance equation to kinetic data. A design analysis method was developed to optimize the removal efficiency and minimum total contact time by combining the time required in the two-stages, in order to achieve the maximum percentage of cadmium and zinc removal using a fixed mass of zeolite. The benefits and limitations of the two-stage design approach have been investigated and discussed

Valorization of aquaculture waste in removal of cadmium from aqueous solution: optimization by kinetics and ANN analysis

Science.gov (United States)

Aditya, Gautam; Hossain, Asif

2018-05-01

Cadmium is one of the most hazardous heavy metal concerning human health and aquatic pollution. The removal of cadmium through biosorption is a feasible option for restoration of the ecosystem health of the contaminated freshwater ecosystems. In compliance with this proposition and considering the efficiency of calcium carbonate as biosorbent, the shell dust of the economically important snail Bellamya bengalensis was tested for the removal of cadmium from aqueous medium. Following use of the flesh as a cheap source of protein, the shells of B. bengalensis made up of CaCO3 are discarded as aquaculture waste. The biosorption was assessed through batch sorption studies along with studies to characterize the morphology and surface structures of waste shell dust. The data on the biosorption were subjected to the artificial neural network (ANN) model for optimization of the process. The biosorption process changed as functions of pH of the solution, concentration of heavy metal, biomass of the adsorbent and time of exposure. The kinetic process was well represented by pseudo second order ( R 2 = 0.998), and Langmuir equilibrium ( R 2 = 0.995) had better fits in the equilibrium process with 30.33 mg g-1 of maximum sorption capacity. The regression equation ( R 2 = 0.948) in the ANN model supports predicted values of Cd removal satisfactorily. The normalized importance analysis in ANN predicts Cd2+ concentration, and pH has the most influence in removal than biomass dose and time. The SEM and EDX studies show clear peaks for Cd confirming the biosorption process while the FTIR study depicts the main functional groups (-OH, C-H, C=O, C=C) responsible for the biosorption process. The study indicated that the waste shell dust can be used as an efficient, low cost, environment friendly, sustainable adsorbent for the removal of cadmium from aqueous solution.

Removal of Cholera Toxin from Aqueous Solution by Probiotic Bacteria

Directory of Open Access Journals (Sweden)

Jussi A. O. Meriluoto

2012-06-01

Full Text Available Cholera remains a serious health problem, especially in developing countries where basic hygiene standards are not met. The symptoms of cholera are caused by cholera toxin, an enterotoxin, which is produced by the bacterium Vibrio cholerae. We have recently shown that human probiotic bacteria are capable of removing cyanobacterial toxins from aqueous solutions. In the present study we investigate the ability of the human probiotic bacteria, Lactobacillus rhamnosus strain GG (ATCC 53103 and Bifidobacterium longum 46 (DSM 14583, to remove cholera toxin from solution in vitro. Lactobacillus rhamnosus strain GG and Bifidobacterium longum 46 were able to remove 68% and 59% of cholera toxin from aqueous solutions during 18 h of incubation at 37 °C, respectively. The effect was dependent on bacterial concentration and L. rhamnosus GG was more effective at lower bacterial concentrations. No significant effect on cholera toxin concentration was observed when nonviable bacteria or bacterial supernatant was used.

Chlorite alteration in aqueous solutions and uranium removal by altered chlorite

Energy Technology Data Exchange (ETDEWEB)

Kim, Eungyeong; Ahn, Hyangsig [Department of Earth and Environmental Sciences, Korea University, Anam-dong, Seongbuk-gu, Seoul 02841 (Korea, Republic of); Jo, Ho Young, E-mail: hyjo@korea.ac.kr [Department of Earth and Environmental Sciences, Korea University, Anam-dong, Seongbuk-gu, Seoul 02841 (Korea, Republic of); Ryu, Ji-Hun; Koh, Yong-Kwon [Korea Atomic Energy Research Institute, 1045 Daedeokdaero, Yuseong-gu, Daejeon 34057 (Korea, Republic of)

2017-04-05

Highlights: • Chlorite alteration and the U removal capacity of altered chlorite were investigated. • Initial pH affected more chlorite dissolution than ionic strength. • Chlorite dissolution at pH{sub o} = 3–8 was inversely proportional to the U removal capacity. • Chlorite dissolution at pH{sub o} = 10 was proportional to the U removal capacity. • The formation of Fe-containing secondary minerals affected the U removal capacity. - Abstract: Chlorite alteration and the U removal capacity of altered chlorite were investigated. Batch kinetic dissolution tests using clinochlore CCa-2 were conducted for 60 days in aqueous solutions of various pHs and ionic strengths. Batch sorption tests using these altered chlorite samples were conducted for 48 h with natural groundwater containing 3.06 × 10{sup −6} M U. Chlorite dissolution was influenced more by pH{sub o} than by the ionic strength of the solution. TEM analysis revealed Fe(oxy)hydroxide aggregates in the solid residue from the batch dissolution test with 0.1 M NaClO{sub 4} solution at pH{sub o} = 10. The U removal capacity of the reacted chlorite samples at pH{sub o} = 6–10 was higher than that of the reacted chlorite samples at pH{sub o} = 3. The degree of dissolution of chlorite samples reacted at pH{sub o} = 3–8 was inversely proportional to the U removal capacity, but that of chlorite samples reacted at pH{sub o} = 10 was proportional to the U removal capacity. The positive correlation between the U removal capacity and degree of chlorite dissolution at pH{sub o} = 10 might be due to the formation of Fe-containing secondary minerals and changes in the reactive sites.

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

Energy Technology Data Exchange (ETDEWEB)

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

2013-11-15

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

Removal of Cu(II) metal ions from aqueous solution by amine functionalized magnetic nanoparticles

Science.gov (United States)

Kothavale, V. P.; Karade, V. C.; Waifalkar, P. P.; Sahoo, Subasa C.; Patil, P. S.; Patil, P. B.

2018-04-01

The adsorption behavior of Cu(II) metal cations was investigated on the amine functionalized magnetic nanoparticles (MNPs). TheMNPs were synthesized by thesolvothermal method and functionalized with (3-Aminopropyl)triethoxysilane (APTES). MNPs were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and vibrating sample magnetometer (VSM). The MNPs have pure magnetite phase with particle size around 10-12 nm. MNPs exhibits superparamagnetic behavior with asaturation magnetization of 68 emu/g. The maximum 38 % removal efficiency was obtained for Cu(II) metal ions from the aqueous solution.

Swift adsorptive removal of Congo red from aqueous solution by K1.33Mn8O16 nanowires.

Science.gov (United States)

Wu, Junshu; Li, Hongyi; Wang, Jinshu; Li, Zhifei

2013-08-01

A swift and efficient approach to converting organic dye effluents into fresh water could be of substantial benefit. In this study, we presented facile hydrothermal synthesis of K1.33Mn8O16 nanowires in ammonium fluoride (NH4F) aqueous solution. The crystallization process of K1.33Mn8O16 nanowires was investigated. The as-obtained K1.33Mn8O16 nanowires were used for swift adsorptive removal of Congo red from aqueous solution without adjusting pH value at room temperature. Adsorption kinetic experimental data are well described by pseudo-second-order rate kinetic model, and the adsorption isotherm fits Langmuir isotherm model. The present investigation provides an efficient approach to designing and fabricating manganese-based nanomaterials for environmental remediation.

Removal of tetracycline from aqueous solution by MCM-41-zeolite A loaded nano zero valent iron: Synthesis, characteristic, adsorption performance and mechanism.

Science.gov (United States)

Guo, Yige; Huang, Wenli; Chen, Bin; Zhao, Ying; Liu, Dongfang; Sun, Yu; Gong, Bin

2017-10-05

In this study, nano zero valent iron (NZVI) modified MCM-41-zeolite A (Fe-MCM-41-A) composite as a novel adsorbent was prepared by precipitation method and applied for tetracycline (TC) removal from aqueous solution. The adsorbent was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and N 2 -BET analysis. Hysteresis loops indicated that the sample has a desirable magnetic property and can be separated quickly. Adsorption studies were carried out to evaluate its potential for TC removal. Results showed that the optimal Fe-MCM-41-A dosage, initial pH and reaction time at initial TC concentration of 100mgL -1 solution are 1gL -1 , pH=5, and 60 min respectively, at which the removal efficiency of TC was 98.7%. The TC adsorption results fitted the Langmuir isotherm model very well and the adsorption process could be described by a pseudo-second-order kinetic model. A maximum TC adsorption capacity of 526.32mgg -1 was achieved. This study demonstrates that Fe-MCM-41-A is a promising and efficient material for TC adsorption from aqueous solution. Copyright © 2017 Elsevier B.V. All rights reserved.

Mercury Removal From Aqueous Solutions With Chitosan-Coated Magnetite Nanoparticles Optimized Using the Box-Behnken Design

Science.gov (United States)

Rahbar, Nadereh; Jahangiri, Alireza; Boumi, Shahin; Khodayar, Mohammad Javad

2014-01-01

Background: Nowadays, removal of heavy metals from the environment is an important problem due to their toxicity. Objectives: In this study, a modified method was used to synthesize chitosan-coated magnetite nanoparticles (CCMN) to be used as a low cost and nontoxic adsorbent. CCMN was then employed to remove Hg2+ from water solutions. Materials and Methods: To remove the highest percentage of mercury ions, the Box-Behnken model of response surface methodology (RSM) was applied to simultaneously optimize all parameters affecting the adsorption process. Studied parameters of the process were pH (5-8), initial metal concentration (2-8 mg/L), and the amount of damped adsorbent (0.25-0.75 g). A second-order mathematical model was developed using regression analysis of experimental data obtained from 15 batch runs. Results: The optimal conditions predicted by the model were pH = 5, initial concentration of mercury ions = 6.2 mg/L, and the amount of damped adsorbent = 0.67 g. Confirmatory testing was performed and the maximum percentage of Hg2+ removed was found to be 99.91%. Kinetic studies of the adsorption process specified the efficiency of the pseudo second-order kinetic model. The adsorption isotherm was well-fitted to both the Langmuir and Freundlich models. Conclusions: CCMN as an excellent adsorbent could remove the mercury ions from water solutions at low and moderate concentrations, which is the usual amount found in environment. PMID:24872943

Silver removal process development for the MEO cleanout

International Nuclear Information System (INIS)

Hsu, P.C.; Chiba, Z.; Schumacher, B.J.; Murguia, L.C.; Adamson, M.G.

1996-02-01

The Mediated Electrochemical Oxidation (MEO) system is an aqueous process which treats low-level mixed wastes by oxidizing the organic components of he waste into carbon dioxide and water. As MEO system continues to run, dissolved ash and radionuclides slowly accumulate in the anolyte and must be removed to maintain process efficiency. At such time, all of the anolyte is pumped into a still feed tank, and the silver ions need to be removed before sending the solution to a thin-film evaporator for further concentration. The efficiency of removing silver ions in the solution needs to be high enough such that the residual silver sent to Final Forms would be less than 1% wt. The purpose of this work is to develop an efficient process to remove silver ions during the MEO cleanout and to demonstrate the capability of centrifugation for separating small silver chloride particles from the solution. This development work includes lab scale experiments and bench scale tests. This report summarizes the results

Removal of copper (II) from aqueous solutions by adsorption onto granular activated carbon in the presence of competitor ions

International Nuclear Information System (INIS)

Almohammadi, S.; Mirzaei, M.

2016-01-01

In this work, the removal of copper from an aqueous solution by granular activated carbon (GAC) in the presence of competitor ions was studied. A batch adsorption was carried out and different parameters such as p H, contact time, initial copper concentration and competitor ions concentration were changed to determine the optimum conditions for adsorption. The optimum p H required for maximum adsorption was found to be 4.5 for copper. Equilibrium was evaluated at 144 h at room temperature. The removal efficiency of Cu(II) was 71.12% at this time. The kinetics of copper adsorption on activated carbon followed the pseudo second-order model. The experimental equilibrium sorption data were tested using the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich (D-R) equations and the Langmuir model was found to be well fitted for copper adsorption onto GAC. The maximum adsorption capacity of the adsorbent for Cu(II) was calculated from the Langmuir isotherm and found to be 7.03 mg/g. Subsequently, the removal of copper by granular activated carbon in the presence of Ag 1 + and Mn 2 + as competitor ions was investigated. The removal efficiency of Cu(II) ions without the presence of the competitor ions was 46% at 6 h, while the removal efficiency of Cu(II) ions in the presence of competitor ions, Ag 1 + and Mn 2 + , was 34.76% and 31.73%, respectevely.

Efficiency of a Photoreactor Packed with Immobilized Titanium Dioxide Nanoparticles in the Removal of Acid Orange 7.

Science.gov (United States)

Sheidaei, Behnaz; Behnajady, Mohammad A

2016-05-01

In this paper, the removal efficiency of Color Index Acid Orange 7 (AO7) as a model contaminant was investigated in a batch-recirculated photoreactor packed with immobilized titanium dioxide type P25 nanoparticles on glass beads. The effects of different operational parameters such as the initial concentration of AO7, the volume of solution, the volumetric flowrate, and the light source power in the photoreactor were investigated. The results indicate that the removal percent increased with the rise in volumetric flowrate and power of the light source, but decreased with the rise of the initial concentration of AO7 and the volume of solution. The AO7 degradation was followed through total organic carbon, gas chromatography/mass spectroscopy (GC/MS), and mineralization products analysis. The ammonium and sulfate ions were analyzed as mineralization products of nitrogen and sulfur heteroatoms, respectively. The results of GC/MS revealed the production of 1-indanone, 1-phthalanone, and 2-naphthalenol as intermediate products for the removal of AO7 in this process.

Photocatalyzed removal of lead ion from lead-chelator solution

Energy Technology Data Exchange (ETDEWEB)

Cho, Young Hyun; Na, Jung Won; Sung, Ki Woung [Korea Atomic Energy Research Institute, Taejon (Korea, Republic of)

1994-07-01

The present study was undertaken to examine the influence of such chelating agents on the ease and speed of photocatalyzed metal removal and deposition. With excess EDTA, the free EDTA competes with Pb for oxidation, and at a ten fold excess, no lead oxidation (hence removal) occurs. With insufficient EDTA, the corresponding initial concentration of Pb-EDTA is decreased; after its destruction, the remaining Pb{sup 2+} is removed more slowly, at rates found with lead nitrate solution. The net result is that the maximum rate of lead deposition occurs at the stoichiometric ratio of 1:1 EDTA : Pb{sup 2+}.

Eosin Removal Properties of Organo-Local Clay from Aqueous Solution

OpenAIRE

Rawan Al-Faze; Fethi Kooli

2014-01-01

Local clay from Al-Madinah Al-Munawwarah was modified by a solution of cetyltrimethylammonium bromide (C16TMABr) at different initial concentrations. The organoclays were characterized by PXRD, TGA, FTIR and N2 adsorption isotherms. The ability of these samples to remove the dye eosin is evaluated. The removal properties of organoclays were dependent on the content of C16TMA cations, the initial concentrations of eosin, temperature of the removal process, the mass of the used organoclays. T...

Removal of methylene blue from aqueous solution with magnetite loaded multi-wall carbon nanotube: Kinetic, isotherm and mechanism analysis

International Nuclear Information System (INIS)

Ai, Lunhong; Zhang, Chunying; Liao, Fang; Wang, Yao; Li, Ming; Meng, Lanying; Jiang, Jing

2011-01-01

Highlights: ► M-MWCNTs were synthesized by a facile one-pot solvothermal method and used as an efficient adsorbent for removing toxic dye from aqueous solution. ► The adsorption process was characterized by kinetics and isotherm analysis. ► FTIR analysis was employed to investigate the interactions between M-MWCNTs and dye. - Abstract: In this study, we have demonstrated the efficient removal of cationic dye, methylene blue (MB), from aqueous solution with the one-pot solvothermal synthesized magnetite-loaded multi-walled carbon nanotubes (M-MWCNTs). The as-prepared M-MWCNTs were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infrared (FTIR) spectroscopy. The effects of contact time, initial dye concentration, and solution pH on the adsorption of MB onto M-MWCNTs were systematically studied. It was shown that the MB adsorption was pH-dependent. Adsorption kinetics was best described by the pseudo-second-order model. Equilibrium data were well fitted to the Langmuir isotherm model, yielding maximum monolayer adsorption capacity of 48.06 mg g −1 . FTIR analysis suggested that the adsorption mechanism was possibly attributed to the electrostatic attraction and π–π stacking interactions between MWCNTs and MB.

Study of the removal of cesium from aqueous solutions by graphene oxide

International Nuclear Information System (INIS)

Bueno, Vanessa N.; Rodrigues, Debora F.; Vitta, Patricia B. Di

2013-01-01

Graphene oxide, used in this work, was synthesized from the oxidation of graphite by Hummer method. The experiments were performed in batch and analyzed for the following parameters: contact time, pH, cesium ion concentration in aqueous solution and removing capacity of the graphene oxide. After the experiments the samples were vacuum filtered and the remaining cesium in solution was quantified by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES). The equilibrium was reached after 60 minutes of contact in neutral solution. The percentage of removal was around 80%

Synthesis and Characterization of Mixed Iron-Manganese Oxide Nanoparticles and Their Application for Efficient Nickel Ion Removal from Aqueous Samples

Science.gov (United States)

Serra, Antonio; Monteduro, Anna Grazia; Padmanabhan, Sanosh Kunjalukkal; Licciulli, Antonio; Bonfrate, Valentina; Salvatore, Luca; Calcagnile, Lucio

2017-01-01

Mixed iron-manganese oxide nanoparticles, synthesized by a simple procedure, were used to remove nickel ion from aqueous solutions. Nanostructures, prepared by using different weight percents of manganese, were characterized by transmission electron microscopy, selected area diffraction, X-ray diffraction, Raman spectroscopy, and vibrating sample magnetometry. Adsorption/desorption isotherm curves demonstrated that manganese inclusions enhance the specific surface area three times and the pores volume ten times. This feature was crucial to decontaminate both aqueous samples and food extracts from nickel ion. Efficient removal of Ni2+ was highlighted by the well-known dimethylglyoxime test and by ICP-MS analysis and the possibility of regenerating the nanostructure was obtained by a washing treatment in disodium ethylenediaminetetraacetate solution. PMID:28804670

Removal of Hexavalent Chromium from Aqueous Solutions using ...

African Journals Online (AJOL)

The hexavalent chromium exists in aquatic media as water soluble complex anions and persist. These are concentrated in industrial waste water especially from the tannery industries and release of effluents from industries adversely affects the environment. The removal of heavy metals from aqueous solutions is carried ...

Polypyrrole-polyaniline/Fe{sub 3}O{sub 4} magnetic nanocomposite for the removal of Pb(II) from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Afshar, Amirhossein; Sadjadi, Seyed Abolfazl Seyed; Mollahosseini, Afsaneh; Eskandarian, Mohammad Reza [Iran University of Science and Technology, Tehran (Iran, Islamic Republic of)

2016-02-15

Lead ion which is engaged in aqueous solution has been successfully removed. A novel technique was utilized for the separation and absorption of Pb(II) ions from aqueous solution. Magnetic Fe{sub 3}O{sub 4} coated with newly investigated polypyrrole-polyaniline nanocomposite was used for the removal of extremely noxious Pb(II). Characteristic of the prepared magnetic nanocomposite was done using X-ray diffraction pattern, Field emission scanning electron microscopy (FE-SEM), Fourier transform-infrared spectroscopy (FT-IR) and energy dispersive x-ray spectroscopy (EDX). Up to 100% adsorption was found with 20mg/L Pb(II) aqueous solution in the range of pH=8-10. Adsorption results illustrated that Pb(II) removal efficiency by the nanocomposite increased with an enhance in pH. Adsorption kinetics was best expressed by the pseudo-second-order rate form. Isotherm data fitted well to the Freundlich isotherm model. Upon using HCl and HNO{sub 3}, 75% PPy-PAn/Fe{sub 3}O{sub 4} nanocomposite, desorption experiment showed that regenerated adsorbent can be reused successfully for two successive adsorption-desorption cycles without appreciable loss of its original capacity.

The use of raw and acid-pretreated bivalve mollusk shells to remove metals from aqueous solutions

International Nuclear Information System (INIS)

Liu Yang; Sun Changbin; Xu Jin; Li Youzhi

2009-01-01

Heavy metal removal from industrial wastewater is not only to protect living organisms in the environment but also to conserve resources such as metals and water by enabling their reuse. To overcome the disadvantage of high cost and secondary pollution by the conventional physico-chemical treatment techniques, environmentally benign and low-cost adsorbents are in demand. In this study, the use of raw and acid-pretreated bivalve mollusk shells (BMSs) to remove metals from aqueous solutions with single or mixed metal was evaluated at different BMSs doses, pH and temperatures in batch shaking experiments in laboratory conditions. When the BMSs were used to treat CuSO 4 .5H 2 O solution, the copper sorption capacities of the raw and acid-pretreated BMSs were approximately 38.93 mg/g and 138.95 mg/g, respectively. The copper removal efficiency (CRE) of the raw BMSs became greatly enhanced with increasing initial pH, reaching 99.51% at the initial pH 5. Conversely, the CRE of the acid-pretreated BMSs was maintained at 99.48-99.52% throughout the pH range of 1-5. Furthermore, the CRE values of the raw and acid-pretreated BMSs were not greatly changed when the temperature was varied from 15 deg. C to 40 deg. C. In addition, the CRE value of the raw BMSs was maintained for 12 cycles of sorption-desorption with a CRE of 98.4% being observed in the final cycle. Finally, when the BMSs were used to treat electroplating wastewater, the removal efficiencies (REs) of the raw BMSs were 99.97%, 98.99% and 87% for Fe, Zn and Cu, respectively, whereas the REs of the acid-pretreated BMSs were 99.98%, 99.43% and 92.13%, respectively. Ion exchange experiments revealed that one of mechanisms for metal sorption by the BMSs from aqueous solution is related to ion exchange, especially between the metal ions in the treated solution and Ca 2+ from BMSs. Infrared absorbance spectra analysis indicated that the acid pretreatment led to occurrence of the groups (i.e. -OH, -NH, C=O and S=O) of

The use of raw and acid-pretreated bivalve mollusk shells to remove metals from aqueous solutions.

Science.gov (United States)

Liu, Yang; Sun, Changbin; Xu, Jin; Li, Youzhi

2009-08-30

Heavy metal removal from industrial wastewater is not only to protect living organisms in the environment but also to conserve resources such as metals and water by enabling their reuse. To overcome the disadvantage of high cost and secondary pollution by the conventional physico-chemical treatment techniques, environmentally benign and low-cost adsorbents are in demand. In this study, the use of raw and acid-pretreated bivalve mollusk shells (BMSs) to remove metals from aqueous solutions with single or mixed metal was evaluated at different BMSs doses, pH and temperatures in batch shaking experiments in laboratory conditions. When the BMSs were used to treat CuSO(4)x5H(2)O solution, the copper sorption capacities of the raw and acid-pretreated BMSs were approximately 38.93 mg/g and 138.95 mg/g, respectively. The copper removal efficiency (CRE) of the raw BMSs became greatly enhanced with increasing initial pH, reaching 99.51% at the initial pH 5. Conversely, the CRE of the acid-pretreated BMSs was maintained at 99.48-99.52% throughout the pH range of 1-5. Furthermore, the CRE values of the raw and acid-pretreated BMSs were not greatly changed when the temperature was varied from 15 degrees C to 40 degrees C. In addition, the CRE value of the raw BMSs was maintained for 12 cycles of sorption-desorption with a CRE of 98.4% being observed in the final cycle. Finally, when the BMSs were used to treat electroplating wastewater, the removal efficiencies (REs) of the raw BMSs were 99.97%, 98.99% and 87% for Fe, Zn and Cu, respectively, whereas the REs of the acid-pretreated BMSs were 99.98%, 99.43% and 92.13%, respectively. Ion exchange experiments revealed that one of mechanisms for metal sorption by the BMSs from aqueous solution is related to ion exchange, especially between the metal ions in the treated solution and Ca(2+) from BMSs. Infrared absorbance spectra analysis indicated that the acid pretreatment led to occurrence of the groups (i.e. -OH, -NH, C=O and S

removal of hazardous pollutants from industrial waste solutions using membrane techniques

International Nuclear Information System (INIS)

Selim, Y.T.M.

2001-01-01

the removal of hazardous pollutants from industrial waste solutions is of essential demand field for both scientific and industrial work. the present work includes detailed studies on the possible use of membrane technology especially liquid emulsion membrane for the removal of hazardous pollutants such as; cadmium , cobalt , lead, copper and uranium from different industrial waste solution . this research can be applied for mixed waste problems. the work carried out in this thesis is presented in three main chapters, namely introduction, experimental and results and discussion

Preparation of magnetic MIL-101 (Cr) for efficient removal of ciprofloxacin.

Science.gov (United States)

Bayazit, Şahika Sena; Danalıoğlu, Selen Tuğba; Abdel Salam, Mohamed; Kerkez Kuyumcu, Özge

2017-11-01

Metal organic frameworks are widely used as adsorbent materials in recent years. In this study, the most prepared metal organic framework MIL-101 was prepared by hydrothermal method and featured magnetic property using co-precipitation method Fe 3 O 4 . Then, the prepared composite (MIL-101/Fe 3 O 4 ) was first characterized using XRD, FTIR, SEM-EDS, and surface area analysis, then was used for the adsorptive removal of the most used antibiotic, ciprofloxacin (CIP). The effect of different adsorption variables which may affect the removal of CIP by MIL-101/Fe 3 O 4 was investigated, as well as their adsorbent quantity, initial CIP concentration, pH, temperature, and contact time. The non-linear Langmuir and Freundlich isotherm were applied to experimental data. It was observed that rising solution temperature decreases adsorption efficiency, as the maximum adsorption uptake value was 63.28 mg g -1 at 298 K and 22.93 mg g -1 at 313 K, indicating the exothermic nature of the adsorption. The adsorption was studied kinetically and found to follow the pseudo-second-order kinetic model. The desorption of CIP from the MIL-101/Fe 3 O 4 was investigated using three different eluents, and the results showed that phosphate-buffered solution was the most effective desorption eluent. Graphical abstract Schematic diagram of the preparation steps of MIL-101/Fe3O4.

Modeling of Malachite Green Removal from Aqueous Solutions by Nanoscale Zerovalent Zinc Using Artificial Neural Network

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Wenqian Ruan

2017-12-01

Full Text Available The commercially available nanoscale zerovalent zinc (nZVZ was used as an adsorbent for the removal of malachite green (MG from aqueous solutions. This material was characterized by X-ray diffraction and X-ray photoelectron spectroscopy. The advanced experimental design tools were adopted to study the effect of process parameters (viz. initial pH, temperature, contact time and initial concentration and to reduce number of trials and cost. Response surface methodology and rapidly developing artificial intelligence technologies, i.e., artificial neural network coupled with particle swarm optimization (ANN-PSO and artificial neural network coupled with genetic algorithm (ANN-GA were employed for predicting the optimum process variables and obtaining the maximum removal efficiency of MG. The results showed that the removal efficiency predicted by ANN-GA (94.12% was compatible with the experimental value (90.72%. Furthermore, the Langmuir isotherm was found to be the best model to describe the adsorption of MG onto nZVZ, while the maximum adsorption capacity was calculated to be 1000.00 mg/g. The kinetics for adsorption of MG onto nZVZ was found to follow the pseudo-second-order kinetic model. Thermodynamic parameters (ΔG0, ΔH0 and ΔS0 were calculated from the Van’t Hoff plot of lnKc vs. 1/T in order to discuss the removal mechanism of MG.

Efficient removal of pathogenic bacteria and viruses by multifunctional amine-modified magnetic nanoparticles.

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Zhan, Sihui; Yang, Yang; Shen, Zhiqiang; Shan, Junjun; Li, Yi; Yang, Shanshan; Zhu, Dandan

2014-06-15

A novel amine-functionalized magnetic Fe3O4-SiO2-NH2 nanoparticle was prepared by layer-by-layer method and used for rapid removal of both pathogenic bacteria and viruses from water. The nanoparticles were characterized by TEM, EDS, XRD, XPS, FT-IR, BET surface analysis, magnetic property tests and zeta-potential measurements, respectively, which demonstrated its well-defined core-shell structures and strong magnetic responsivity. Pathogenic bacteria and viruses are often needed to be removed conveniently because of a lot of co-existing conditions. The amine-modified nanoparticles we prepared were attractive for capturing a wide range of pathogens including not only bacteriophage f2 and virus (Poliovirus-1), but also various bacteria such as S. aureus, E. coli O157:H7, P. aeruginosa, Salmonella, and B. subtilis. Using as-prepared amine-functionalized MNPs as absorbent, the nonspecific removal efficiency of E. coli O157:H7 or virus was more than 97.39%, while it is only 29.8% with Fe3O4-SiO2 particles. From joint removal test of bacteria and virus, there are over 95.03% harmful E. coli O157:H7 that can be removed from mixed solution with polyclonal anti-E. coli O157:H7 antibody modified nanoparticles. Moreover, the synergy effective mechanism has also been suggested. Copyright © 2014 Elsevier B.V. All rights reserved.

Comparision of Chitosan Function as Adsorbent for Nitrate Removal Using Synthetic Aqueous Solution and Drinking Water

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Mohammad Norisepehr

2013-12-01

Full Text Available Background & Objectives: Nitrate and nitrite compounds pollution of groundwater resources in recent years which recently their mean concentration due to enhancement of different kind of municipal, industrial and agriculture waste water, were increased. The most common source of nitrates entering the water include chemical fertilizers and animal manure in agriculture, septic tank effluent, wastewater, wastewater treatment plants, animal and plant residue analysis on the ground of non-sanitary disposal of solid waste and the use of absorbing wells for sewage disposal. Materials and methods: This experimental study is applied to the nitrate removal using chitosan in laboratory scale at ambient temperature and the design of the system was Batch. Effects of parameters such as pH, contact time, initial concentration and adsorbent concentration of nitrate on nitrate removal from aqueous solution was studied. Results: Function of chitosan in synthetic aqueous solution and drinking water according to the slurry system results, the optimum condition was obtained at pH=4, 20 min contact time and increasing the initial concentration of nitrate enhance the adsorption capacity of chitosan. Also optimum dosage of adsorbent was obtained at 0.5 g/l. The data obtained from the experiments of adsorbent isotherm were analyzed using Langmuir and Freundlich isotherm models. The Langmuir equation was found to be the best fitness with the experimental data (R2>0.93. Conclusion: Although efficiency of Nitrate removal in synthetic aqueous solution was better than drinking water, adsorption process using chitosan as an option for the design and selection nitrate removal should be considered in order to achieve environmental standards.

Remarkable efficiency of phosphate removal: Ferrate(VI)-induced in situ sorption on core-shell nanoparticles.

Science.gov (United States)

Kralchevska, Radina P; Prucek, Robert; Kolařík, Jan; Tuček, Jiří; Machala, Libor; Filip, Jan; Sharma, Virender K; Zbořil, Radek

2016-10-15

Despite the importance of phosphorus as a nutrient for humans and its role in ecological sustainability, its high abundance, resulting in large part from human activities, causes eutrophication that negatively affects the environment and public health. Here, we present the use of ferrate(VI) as an alternative agent for removing phosphorus from aqueous media. We address the mechanism of phosphate removal as a function of the Fe/P mass ratio and the pH value of the solution. The isoelectric point of γ-Fe2O3 nanoparticles, formed as dominant Fe(VI) decomposition products, was identified to play a crucial role in predicting their efficiency in removing of phosphates. Importantly, it was found that the removal efficiency dramatically changes if Fe(VI) is added before (ex-situ conditions) or after (in-situ conditions) the introduction of phosphates into water. Removal under in-situ conditions showed remarkable sorption capacity of 143.4 mg P per gram of ferric precipitates due to better accessibility of active surface sites on in-situ formed ferric oxides/oxyhydroxides. At pH = 6.0-7.0, complete removal of phosphates was observed at a relatively low Fe/P mass ratio (5:1). The results show that phosphates are removed from water solely by sorption on the surface of γ-Fe2O3/γ-FeOOH core/shell nanoparticles. The advantages of Fe(VI) utilization include its environmentally friendly nature, the possibility of easy separation of the final product from water by a magnetic field or by natural settling, and the capacity for successful phosphate elimination at pH values near the neutral range and at low Fe/P mass ratios. Copyright © 2016 Elsevier Ltd. All rights reserved.

Efficiency of lead removal from drinking water using cationic resin Purolite

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Ashour Mohammad Merganpour

2015-01-01

Full Text Available Background: Today, issues such as water shortage, difficulties and costs related to supplying safe water, and anomalous concentrations of heavy metals in groundwater and surface water resources, doubled the necessity of access to technical methods on removing these pollutants from water resources. Methods: In this lab study, cationic resin Purolite S-930 (with co-polymer styrene di-vinyl benzene structure was used for lead removal from drinking water containing up to 22 μg/L. Using statistical analysis and designing a full factorial experiment are the most important effective parameters on lead removal obtained through ion exchange process. Results: Analysis of response and interaction parameters of ion exchange showed that the resin column height has maximum and pH value has minimum effect on the efficiency of lead removal from aquatic environment. Trinary interaction of “effective size, flow rate, resin column high” has the most important for lead removal efficiency in this system. So the maximum efficiency was obtained at the mesh = 40, bed height =1.6 meter, and pH= 6.5. At the best operation conditions, ability to remove 95.42% of lead concentration can be achieved. Conclusion: Using the resin Purolite S-930 during 21-day service with 91.12% of mean lead removal ratio from drinking water is an economic and technical feasibility.

Effective removal of hexavalent mercury from aqueous solution by modified polymeric nanoadsorbent

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Lida Rahmanzadeh

2016-07-01

Full Text Available Mercury is one of the most toxic metals present in the environment. Adsorption has been proposed among the technologies for mercury adsorbent. The kinetics of adsorption depends on the adsorbent concentration, and the physical and chemical characteristics of adsorbent. In this study we were used a novel adsorbent, magnetite-polyrhodanine core- shell nanoparticles, for removing Hg(II from aqueous solution. The effect of pH, initial Hg(II concentration, initial adsorbent concentration and contact time on the efficiency of Hg(II removal were investigated systematically by batch experiments. The maximum adsorption capacity was obtained 29.14 mg g-1 at PH=6.5 and 25°C with 10 g L-1 nano adsorbent. The kinetic data of adsorption of Hg(II ion on the synthesized adsorbent were best described by a pseudo- second- order equation, indicating their chemical adsorption. The Freundlich, Langmuir and Temkin isotherms were used to modeling of mercury adsorption on Hg(II in aqueous medium which modeled best by the Freundlich isotherm is whole concentration rage.

Performance of ultrasonic and hydrogen peroxide technologies in removal of Bisphenol A from Aqueous solution

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MH Dehghani

2016-05-01

Full Text Available Introduction:BPA is a non biodegradable antioxidant that has greatly hazardous for human and animals health. and Because of the eliminating alone fewness amount of the BPA during the wastewater treatment, wastewater that contains BPA can be source of pollution in aqueous solution. The objective of this study was Performance of ultrasonic and H2O2 technologies in removal of BPA from aqueous solution. Methods:Experiments of sonochemical was carried out with use of unit ultrasonicator (Elma, which in the two power 300 and 500W, frequencies at 35 and 130KHz. Hydrogen Peroxide in concentrations at 5, 15 and 30mg/lit was applied. Initial concentration BPA at limits 2, 5, 20 and 50 mg/lit which For measuring concentration of BPA used from Spectrometer UV/VIS Lambada 25 Perkin Elmer, Shelton unit. Results:The results demonstrated that hybrid ultrasonic and peroxide Hydrogen processes with Efficiency 98.65%,  has the highest efficiency in the removal of BPA. The most decomposition rate achieved at the frequency of 130 KHz and 500W assisted by 30mg/lit H2O2 at pH 11. Also the results demonstrated that with pH increase destruction rate BPA the increased by any three processes (ultrasonic, H2O2 and both hybrid. Conclusion:The results demonstrated that hybrid ultrasonic and peroxide Hydrogen processes can be used as a clean method and friendly environment for waters treatment are contains desirable BPA.

The efficiency of biosynthesis silica nanoparticles at removal of heavy metals Cr and Cu from aqueous solutions

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Mohammad Hossein Sayadi

2017-05-01

Full Text Available Background and Aim: Nanotechnology considered as one of the main management strategy in reducing negative effects of water pollution, which leads to treating of water inexpensive and more effective. This study aimed to investigate the removal of Cr and Cu from aqueous solutions using nano-silicate which is synthesized by rice husk. Materials and Methods: In the present study, functionalized nano-silica with rice husk was fabricated and characterized by FT-IR، TEM, SEM and XRD. The effect of adsorbent dosage, initial concentration and equilibrium of chromium and copper and contact time in removal of mentioned heavy metals were investigated. Finally, the adsorption isotherms were analyzed. Results: The silica nanoparticles had nearly spherical morphology with a uniform size of about 80 nm. However, the obtained functionalized silica nanoparticles were spherical (about 90 nm in diameter. Results showed that optimum adsorption of Cr and Cu contaminant obtained at 100 minutes, while the optimum amount of adsorbent for Cr and Cu were 125 and 100 mg respectively. The optimal concentration of Cr and Cu was 2 mg/l. The correlation coefficients of adsorption isotherms of Cr (R2Langmuir =0.9946 and Cu (R2Langmuir =0.999 showed the good agreement between the adsorption data and Langmuir model. Conclusion: The study showed that the silica nanoparticles can be produced using agricultural waste as a inexpensive and environmentally friendly method and can be used to removing of contaminants from the aquatic environment.

Solution of heat removal from nuclear reactors by natural convection

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Zitek Pavel

2014-03-01

Full Text Available This paper summarizes the basis for the solution of heat removal by natural convection from both conventional nuclear reactors and reactors with fuel flowing coolant (such as reactors with molten fluoride salts MSR.The possibility of intensification of heat removal through gas lift is focused on. It might be used in an MSR (Molten Salt Reactor for cleaning the salt mixture of degassed fission products and therefore eliminating problems with iodine pitting. Heat removal by natural convection and its intensification increases significantly the safety of nuclear reactors. Simultaneously the heat removal also solves problems with lifetime of pumps in the primary circuit of high-temperature reactors.

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

International Nuclear Information System (INIS)

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

2004-01-01

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

Hg(II) removal from aqueous solutions by bacillus subtilis biomass

Energy Technology Data Exchange (ETDEWEB)

Wang, Xue Song; Li, Fei Yan; He, Wen; Miao, Hua Hua [Department of Chemical Engineering, Huaihai Institute of Technology, Lianyungang (China)

2010-01-15

The biosorption of Hg(II) from aqueous solutions using Bacillus subtilis biomass was investigated in this study. The adsorbent was characterized by FTIR. Various factors including solution pH, initial concentration of Hg(II), contact time, reaction temperature and ionic strength were taken into account and promising results were obtained. An initial solution pH of 5.0 was most favorable for Hg(II) removal. The kinetic data was also analyzed using pseudo first order and pseudo second order equations. The results suggested that Hg(II) bioadsorption was best represented by the pseudo second order equation. Freundlich, Langmuir and Langmuir-Freundlich isotherms for the present systems were analyzed. The most satisfactory interpretation for the equilibrium data at different temperatures was given by the Langmuir-Freundlich isotherm. The effect of ionic strength on bioadsorption was significant. Bacillus subtilis biomass could serve as low cost adsorbent to remove Hg(II) from aqueous solutions, especially at lower concentrations of Hg(II) (<20 mg Hg/L). (Abstract Copyright [2010], Wiley Periodicals, Inc.)

Removal of copper (II from aqueous solutions by adsorption onto granular activated carbon in the presence of competitor ions

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Saeed Almohammadi

2016-04-01

Full Text Available In this work, the removal of copper from an aqueous solution by granular activated carbon (GAC in the presence of competitor ions was studied. A batch adsorption was carried out and different parameters such as pH, contact time, initial copper concentration and competitor ions concentration were changed to determine the optimum conditions for adsorption. The optimum pH required for maximum adsorption was found to be 4.5 for copper. Equilibrium was evaluated at 144 h at room temperature. The removal efficiency of Cu(II was 71.12% at this time. The kinetics of copper adsorption on activated carbon followed the pseudo second-order model. The experimental equilibrium sorption data were tested using the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich (D-R equations and the Langmuir model was found to be well fitted for copper adsorption onto GAC. The maximum adsorption capacity of the adsorbent for Cu(II was calculated from the Langmuir isotherm and found to be 7.03 mg/g. Subsequently, the removal of copper by granular activated carbon in the presence of Ag1+ and Mn2+ as competitor ions was investigated. The removal efficiency of Cu(II ions without the presence of the competitor ions was 46% at 6 h, while the removal efficiency of Cu(II ions in the presence of competitor ions, Ag1+ and Mn2+ , was 34.76% and 31.73%, respectively.

2-Chlorophenol Removal of Aqueous Solution Using Advanced Oxidation Processes Resulting from Iron/ Persulfate and Ultra Violet/ Persulfate

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Shokufeh Astereki

2016-06-01

Full Text Available Background: Advanced oxidation processes are used to remove toxic aromatic compounds with low biodegradability, such as 2-chlorophenol. This study investigated the use of sulfate (SO4- and persulfate (S2O82- radicals, as one of the advanced oxidation methods, to remove 2- chlorophenol from aquatic solutions. Methods: This experimental and pilot-scale study was carried out using two chemical batch reactors; one of the reactors equipped with UV lamps and the other was on the hot plate. In iron/ persulfate (Fe/S2O82- and ultra violet/ persulfate (UV/S2O82- processes different parameters were investigated. Results: Iron, UV, the initial pH of the solution, persulfate concentration have considerable effects on the elimination of 2-chlorophenol in both processes. In both processes, the maximum elimination occurred in acidic conditions. The elimination efficiency was increased by increasing the concentration of 2-chlorophenol and UV intensity, and also by decreasing the concentration of persulfate and iron. Accordingly, in iron/ persulfate and ultra violet/ persulfate processes 2-chlorophenol was eliminated with 99.96% and 99.58% efficiencies, respectively. Conclusion: Sulfate radicals produced from activated persulfate ions with hot-Fe ion and UV radiation have significant impact on the removal of 2-chlorophenol. Therefore, the processes of Fe/S2O82- and UV/S2O82- can be regarded as good choices for industrial wastewater treatment plants operators in the future.

Removal of ammonia solutions used in catalytic wet oxidation processes.

Science.gov (United States)

Hung, Chang Mao; Lou, Jie Chung; Lin, Chia Hua

2003-08-01

Ammonia (NH(3)) is an important product used in the chemical industry, and is common place in industrial wastewater. Industrial wastewater containing ammonia is generally either toxic or has concentrations or temperatures such that direct biological treatment is unfeasible. This investigation used aqueous solutions containing more of ammonia for catalytic liquid-phase oxidation in a trickle-bed reactor (TBR) based on Cu/La/Ce composite catalysts, prepared by co-precipitation of Cu(NO(3))(2), La(NO(3))(2), and Ce(NO(3))(3) at 7:2:1 molar concentrations. The experimental results indicated that the ammonia conversion of the wet oxidation in the presence of the Cu/La/Ce composite catalysts was determined by the Cu/La/Ce catalyst. Minimal ammonia was removed from the solution by the wet oxidation in the absence of any catalyst, while approximately 91% ammonia removal was achieved by wet oxidation over the Cu/La/Ce catalyst at 230 degrees C with oxygen partial pressure of 2.0 MPa. Furthermore, the effluent streams were conducted at a liquid hourly space velocity of under 9 h(-1) in the wet catalytic processes, and a reaction pathway was found linking the oxidizing ammonia to nitric oxide, nitrogen and water. The solution contained by-products, including nitrates and nitrites. Nitrite selectivity was minimized and ammonia removal maximized when the feed ammonia solution had a pH of around 12.0.

Evaluation of the Efficiency of Clay Pots in Removal of Water Impurities

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K Naddafi , AH Mahvi, S Nasseri, M Mokhtari, H Zeraati

2005-04-01

Full Text Available Recently, inexpensive technologies for drinking water supply in small communities are highly considered in developing countries. One of these technologies is the application of ceramic filters that are usually made of diatomaceous earth or clay soil. This research was carried out to determine the efficiency of clay pots (as a filter in removing water impurities. Pilot and the related clay parts were manufactured and its efficiency in removing TDS, hardness, NO3-, color and turbidity was measured by passing water through the clay pipes. The results showed that the clay filters had not the potential to remove hardness, EC, TDS and nitrate of water. However, they showed excellent efficiency in turbidity removal (≥ 90% and could significantly decrease the color of the water (≥ 60%.

Removal of COD from laundry wastewater by electrocoagulation/electroflotation

International Nuclear Information System (INIS)

Wang, C.-T.; Chou, W.-L.; Kuo, Y.-M.

2009-01-01

The removal efficiency of COD in the treatment of simulated laundry wastewater using electrocoagulation/electroflotation technology is described. The experimental results showed that the removal efficiency was better, reaching to about 62%, when applying ultrasound to the electrocoagulation cell. The solution pH approached neutrality in all experimental runs. The optimal removal efficiency of COD was obtained by using the applied voltage of 5 V when considering the energy efficiency and the acceptable removal efficiency simultaneously. The Cl - concentration of less than 2500 ppm had a positive effect on the removal efficiency. The performance of the monopolar connection of electrodes was better than that of the bipolar connection in this work. In addition, the removal efficiency of using Al electrodes was higher in comparison with using Fe electrodes in the study. The highest COD removal amount per joule was found to be 999 mg dm -3 kW h -1 while using two Al electrodes, although the removal efficiency increased with the number of Al plates

Removal of Reactive Dyes (Green, Orange, and Yellow from Aqueous Solutions by Peanut Shell Powder as a Natural Adsorbent

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Hosein Nadi

2012-11-01

Full Text Available Please cite this article as: Nadi H, Alizadeh M, Ahmadabadi M, Yari AR, Hashemi S. Removal of Reactive Dyes (Green, Orange, and Yellow from Aqueous Solutions by Peanut Shell Powder as a Natural Adsorbent. Arch Hyg Sci 2012;1(2:41-7. Abstract: Background & Aims of the Study: Textile dyes generally are made of synthetic, organic, and aromatic compounds that may be contain of some heavy metals in their structure. Complex structure and presence of these metals cause toxicity and may be mutagen, teratogen or carcinogen. This study has investigated the ability of peanut shell powder to removal of some reactive dyes (Green 19, Orange 16, and Yellow 14 from aqueous solutions. Materials & Methods : The effects of contact time, initial concentration of reactive dyes, adsorbent dosage and pH have been reported. The applicability of Langmuir and Freundlich isotherm was tried for the system to completely understand the adsorption isotherm processes. Results: Batch adsorption studies showed that the peanut shell powder was able to remove the reactive dyes from aqueous solutions in the concentration range 25 to 250 mg/L. The highest percent removal for the Green 19, Orange 16, and Yellow 14 dyes was 84.2%, 87.36% and 88.49%, respectively. The adsorption was favored with maximum adsorption at pH=2. Also the optimum adsorbent dose was obtained 0.4 g/100 mL. By increasing adsorbent dose and initial concentration, removal efficiency was increased considerably. The adsorption isotherm studies clearly indicated that the adsorptive behavior of dyes on peanut shell satisfies only the Freundlich with average R 2 =0.926. Conclusions: Based on findings, the peanut shell powder was found as a low cost, natural and abundant availability adsorbent to removal of reactive dyes from aqueous solution. References: 1. García-Montaño J, Torrades F, García-Hortal JA, Domènec X, Peral J. Combining photo-Fenton process with aerobic sequencing batch reactor for commercial hetero

Synthesis and Characterization of Mixed Iron-Manganese Oxide Nanoparticles and Their Application for Efficient Nickel Ion Removal from Aqueous Samples

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Alessandro Buccolieri

2017-01-01

Full Text Available Mixed iron-manganese oxide nanoparticles, synthesized by a simple procedure, were used to remove nickel ion from aqueous solutions. Nanostructures, prepared by using different weight percents of manganese, were characterized by transmission electron microscopy, selected area diffraction, X-ray diffraction, Raman spectroscopy, and vibrating sample magnetometry. Adsorption/desorption isotherm curves demonstrated that manganese inclusions enhance the specific surface area three times and the pores volume ten times. This feature was crucial to decontaminate both aqueous samples and food extracts from nickel ion. Efficient removal of Ni2+ was highlighted by the well-known dimethylglyoxime test and by ICP-MS analysis and the possibility of regenerating the nanostructure was obtained by a washing treatment in disodium ethylenediaminetetraacetate solution.

Usefulness of ANN-based model for copper removal from aqueous solutions using agro industrial waste materials

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Petrović Marija S.

2015-01-01

Full Text Available The purpose of this study was to investigate the adsorption properties of locally available lignocelluloses biomaterials as biosorbents for the removal of copper ions from aqueous solution. Materials are generated from juice production (apricot stones and from the corn milling process (corn cob. Such solid wastes have little or no economic value and very often present a disposal problem. Using batch adsorption techniques the effects of initial Cu(II ions concentration (Ci, amount of biomass (m and volume of metal solution (V, on biosorption efficiency and capacity were studied for both materials, without any pre-treatments. The optimal parameters for both biosorbents were selected depending on a highest sorption capability of biosorbent, in removal of Cu(II. Experimental data were compared with second order polynomial regression models (SOPs and artificial neural networks (ANNs. SOPs showed acceptable coefficients of determination (0.842 - 0.997, while ANNs performed high prediction accuracy (0.980-0.986 in comparison to experimental results. [Projekat Ministarstva nauke Republike Srbije, br. TR 31003, TR 31055

Synthesis and Application of Iron Oxide/Silica Gel Nanocomposite for Removal of Sulfur Dyes from Aqueous Solutions

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Naser Tavassoli

2017-03-01

Full Text Available Background & Aims of the Study: water pollution by synthetic organic dyes is mainly regarded as environmental and ecological critical issues worldwide. In this research, magnetite iron oxide/silica gel nanocomposite (termed as Fe3O4/SG was synthesized chemically and then used as an effective adsorbent for removal of sulfur dyes from aqueous solution. Materials and Methods: The various parameters such as pH, sorbent dosage, initial dye concentration, contact time and dye solution temperature were investigated in a batch system. The equilibrium data were analyzed by Langmuir and Freundlich isotherm models. Results: The experimental data fit well with pseudo-second-order kinetic model (R2≥0.998 and conformed better to Langmuir isotherm model (R2≥0.997. The maximum adsorption capacity for Fe3O4/SG obtained from the Langmuir model was 11.1mg/g. Evaluation of thermodynamic parameters proved that the adsorption process was normally feasible, spontaneous and exothermic. Conclusion: It can be concluded that the Fe3O4/SG can be considered as a cost-effective and an environmental friendly adsorbent for efficient removal of sulfur dyes from aqueous solutions.

Heavy metal removal from aqueous solutions using engineered magnetic biochars derived from waste marine macro-algal biomass.

Science.gov (United States)

Son, Eun-Bi; Poo, Kyung-Min; Chang, Jae-Soo; Chae, Kyu-Jung

2018-02-15

Despite the excellent sorption ability of biochar for heavy metals, it is difficult to separate and reuse after adsorption when applied to wastewater treatment process. To overcome these drawbacks, we developed an engineered magnetic biochar by pyrolyzing waste marine macro-algae as a feedstock, and we doped iron oxide particles (e.g., magnetite, maghemite) to impart magnetism. The physicochemical characteristics and adsorption properties of the biochar were evaluated. When compared to conventional pinewood sawdust biochar, the waste marine algae-based magnetic biochar exhibited a greater potential to remove heavy metals despite having a lower surface area (0.97m 2 /g for kelp magnetic biochar and 63.33m 2 /g for hijikia magnetic biochar). Although magnetic biochar could be effectively separated from the solution, however, the magnetization of the biochar partially reduced its heavy metal adsorption efficiency due to the biochar's surface pores becoming plugged with iron oxide particles. Therefore, it is vital to determine the optimum amount of iron doping that maximizes the biochar's separation without sacrificing its heavy metal adsorption efficiency. The optimum concentration of the iron loading solution for the magnetic biochar was determined to be 0.025-0.05mol/L. The magnetic biochar's heavy metal adsorption capability is considerably higher than that of other types of biochar reported previously. Further, it demonstrated a high selectivity for copper, showing two-fold greater removal (69.37mg/g for kelp magnetic biochar and 63.52mg/g for hijikia magnetic biochar) than zinc and cadmium. This high heavy metal removal performance can likely be attributed to the abundant presence of various oxygen-containing functional groups (COOH and OH) on the magnetic biochar, which serve as potential adsorption sites for heavy metals. The unique features of its high heavy metal removal performance and easy separation suggest that the magnetic algae biochar can potentially

Effect of adsorbents and chemical treatments on the removal of strontium from aqueous solutions

International Nuclear Information System (INIS)

Ahmadpour, A.; Zabihi, M.; Tahmasbi, M.; Bastami, T. Rohani

2010-01-01

In the present investigation, three different solid wastes namely almond green hull, eggplant hull, and moss were initially treated and used as adsorbents for the adsorption of strontium ion from aqueous solutions. Adsorbent types and chemical treatments are proved to have effective roles on the adsorption of Sr(II) ion. Among the three adsorbents, almond green hull demonstrated strong affinity toward strontium ion in different solutions. The effectiveness of this new adsorbent was studied in batch adsorption mode under a variety of experimental conditions such as: different chemical treatments, various amounts of adsorbent, and initial metal-ion concentration. The optimum doses of adsorbent for the maximum Sr(II) adsorption were found to be 0.2 and 0.3 g for 45 and 102 mg L -1 solutions, respectively. High Sr(II) adsorption efficiencies were achieved only in the first 3 min of adsorbent's contact time. The kinetics of Sr(II) adsorption on almond green hull was also examined and it was observed that it follows the pseudo second-order behavior. Both Langmuir and Freundlich models well predicted the experimental adsorption isotherm data. The maximum adsorption capacity on almond green hull was found to be 116.3 mg g -1 . The present study also confirmed that these low cost agriculture byproducts could be used as efficient adsorbents for the removal of strontium from wastewater streams.

Highly efficient removal of arsenic metal ions with high superficial area hollow magnetite nanoparticles synthetized by AACVD method

Energy Technology Data Exchange (ETDEWEB)

Monárrez-Cordero, B.; Amézaga-Madrid, P.; Antúnez-Flores, W.; Leyva-Porras, C.; Pizá-Ruiz, P. [Centro de Investigación en Materiales Avanzados S.C., and Laboratorio Nacional de Nanotecnología, Miguel de Cervantes 120, Chihuahua, Chih. C.P. 31109 (Mexico); Miki-Yoshida, M., E-mail: mario.miki@cimav.edu.mx [Centro de Investigación en Materiales Avanzados S.C., and Laboratorio Nacional de Nanotecnología, Miguel de Cervantes 120, Chihuahua, Chih. C.P. 31109 (Mexico)

2014-02-15

Highlights: ► Fast and high arsenic removal efficiency, almost 100% in one minute. ► Successful synthesis of high purity magnetite hollow nanoparticles is reported. ► They were synthesized by one step aerosol assisted CVD technique. ► Detailed microstructural characterization by electron microscopy was performed. -- Abstract: New nanotechnology alternatives and methodologies have been developed in order to overcome the limitations of conventional techniques for metal ions removal from water. Currently, the removal of heavy metals requires multiple steps which include the separation and post-treatment of the generated sludge. Usually, this sludge is composed of dangerous environmental pollutants mixed with the material used for removing the metal ion. Thus, the removal of these metals becomes a challenging task. Herein we report the synthesis of magnetite nanoparticles with high specific area by the aerosol assisted chemical vapour deposition method. Deposition temperature were fixed at 450 °C and a mixture of Ar–air were used as a carrier gas, a flow of 1.0 and 0.015 L min{sup −1} were used for Ar and air, respectively. The precursor solution was a dilution of Fe (II) chloride in methanol, with different concentration 0.01, 0.05 and 0.1 mol dm{sup −3}. The crystalline structure of the nanoparticles was characterized by grazing incidence X-ray diffraction. Morphology and microstructure were analyzed by field emission scanning electron microscopy, scanning probe microscopy and transmission electron microscopy. Magnetic properties were evaluated with a vibrating sample magnetometer and specific area was measured by the Brunauer–Emmett–Teller method. To determine the removal efficiency of arsenic ion from water, several tests were carried out at six exposition times 1, 3, 5, 10, 20 and 30 min. Results showed high removal efficiency, more than 99%, in less than 1 min.

Mercury removal from solution by superconducting magnetic separation with nanostructured magnetic adsorbents

Energy Technology Data Exchange (ETDEWEB)

Okamoto, T., E-mail: okamoto-takayuki@ed.tmu.ac.jp [Graduate School of Science and Engineering, Tokyo Metropolitan University, 1-1 Minami-Osawa, Hachioji, Tokyo 192-0397 (Japan); Tachibana, S.; Miura, O. [Graduate School of Science and Engineering, Tokyo Metropolitan University, 1-1 Minami-Osawa, Hachioji, Tokyo 192-0397 (Japan); Takeuchi, M. [Komazawa Jin Clinic, 1-19-8 Komazawa, Setagayaku, Tokyo 154-0012 (Japan)

2011-11-15

Recently, mercury Hg concentration in human blood increases due to expanding the global mercury contamination. Excess mercury bioaccumulation poses a significant health risk. In order to decrease mercury concentration in the environment and human blood, we have developed two different kinds of nanostructured magnetic adsorbents for mercury to apply them to superconducting magnetic separation instead of conventional filtration. One is magnetic beads (MBs) which have nanosize magnetite particles in the core and a lot of SH radicals on the surface to adsorb Hg ions effectively. MBs were developed mainly to remove mercury from human blood. The maximum amount of the adsorption for MBs is 6.3 mg/g in the solution in less than a minute. Dithiothreitol can easily remove mercury adsorbed to MBs, hence MBs can be reusable. The other is nanostructured magnetic activated carbon (MAC) which is activated carbon with mesopores and nanosize magnetite. The maximum amount of the adsorption for MAC is 38.3 mg/g in the solution. By heat-treatment mercury can be easily removed from MAC. We have studied superconducting magnetic separation using each adsorbent for mercury removal from solution.

Influences of impurities on iodine removal efficiency of silver alumina adsorbent

Energy Technology Data Exchange (ETDEWEB)

Fukasawa, Tetsuo; Funabashi, Kiyomi [Hitachi, Ltd., Ibaraki (Japan); Kondo, Yoshikazu [Hitachi, Ltd., Ibaraki (Japan)

1997-08-01

Silver impregnated alumina adsorbent (AgA), which was developed for iodine removal from off-gas of nuclear power and reprocessing plants has been tested laying emphasis on investigation of the influences gaseous impurities have on adsorbent chemical stability and iodine removal efficiency. The influences of the major impurities such as nitrogen oxides and water vapor were checked on the chemical state of impregnated silver compound (AgNO{sub 3}) and decontamination factor (DF) value. At 150{degrees}C, a forced air flow with 1.5% nitrogen oxide (NO/NO{sub 2}=1/1) reduced silver nitrate to metallic silver, whereas pure air and air with 1.5% NO{sub 2} had no effect on the chemical state of silver. Metallic silver showed a lower DF value for methyl iodide in pure air (without impurities) than silver nitrate and the lower DF of metallic silver was improved when impurities were added. At 40{degrees}C, a forced air flow with 1.5% nitrogen dioxide (NO{sub 2}) increased the AgA weight by about 20%, which was caused by the adsorption of nitric acid solution on the AgA surface. AgA with l0wt% silver showed higher weight increase than that with 24wt% silver which had lower porosity. Adsorption of acid solution lowered the DF value, which would be due to the hindrance of contact between methyl iodide and silver. The influences of other gaseous impurities were also investigated and AgA showed superior characteristics at high temperatures. 14 refs., 11 figs.

Removal of Metal Nanoparticles Colloidal Solutions by Water Plants

Science.gov (United States)

Olkhovych, Olga; Svietlova, Nataliia; Konotop, Yevheniia; Karaushu, Olena; Hrechishkina, Svitlana

2016-11-01

The ability of seven species of aquatic plants ( Elodea canadensis, Najas guadelupensis, Vallisneria spiralis L., Riccia fluitans L., Limnobium laevigatum, Pistia stratiotes L., and Salvinia natans L.) to absorb metal nanoparticles from colloidal solutions was studied. It was established that investigated aquatic plants have a high capacity for removal of metal nanoparticles from aqueous solution (30-100%) which indicates their high phytoremediation potential. Analysis of the water samples content for elements including the mixture of colloidal solutions of metal nanoparticles (Mn, Cu, Zn, Ag + Ag2O) before and after exposure to plants showed no significant differences when using submerged or free-floating hydrophytes so-called pleuston. However, it was found that the presence of submerged hydrophytes in aqueous medium ( E. canadensis, N. guadelupensis, V. spiralis L., and R. fluitans L.) and significant changes in the content of photosynthetic pigments, unlike free-floating hydrophytes ( L. laevigatum, P. stratiotes L., S. natans L.), had occur. Pleuston possesses higher potential for phytoremediation of contaminated water basins polluted by metal nanoparticles. In terms of removal of nanoparticles among studied free-floating hydrophytes, P. stratiotes L. and S. natans L. deserve on special attention.

Hydraulic washing removal efficiencies of Orimulsion from rock surfaces

International Nuclear Information System (INIS)

Harper, J.R.; Ward, S.; Sergy, G.

2002-01-01

Orimulsion is a fuel alternative composed of 70 per cent bitumen in 30 per cent water. It is shipped from Venezuela to New Brunswick where it is used as fuel oil for power plants. While there have not been any major spills of Orimulsion, it is recognized that very little is known regarding the dispersal and weathering processes of Orimulsion, or the behaviour and cleanup of the product on both rocky and course sediment shorelines. For that reason, this study was conducted to determine the efficiency of hydraulic washing under different water temperatures and pressures to remove bitumen from rocky shorelines. The results of the study make it possible to assess the physical effectiveness of the method and to determine the range of effective operational parameters. The coating protocol was refined to create uniform coating of both dispersed and coalesced bitumen of rock surfaces. The use of a chemical agent for enhancing removal efficiency was also assessed. Orimulsion could reach shorelines as low concentration dispersions of bitumen particles suspended in a water column, or as a high concentration mixture of bitumen, water and air. Granite tiles were coated with uniform coatings of both dispersed and coalesced bitumen. They were then washed under different pressures, temperatures and other treatments. Temperatures of more than 40 degrees C and pressures of more than 76 kPa were needed to effectively remove the bitumen coatings. Weathering significantly increased coating tenacity for dispersed coatings, but did not affect coalesced coating tenacity. Immediate washing was found to be very effective for removing dispersed coating, but not for coalesced coating. Coating tenacity was also affected by submergence times. Pre-treatment of the coating with a dispersion called Corexit significantly improved the removal efficiencies of dispersed coatings, but not coalesced coatings. 6 refs., 10 tabs., 5 figs

Enzymatic removal of estrogenic activity of nonylphenol and octylphenol aqueous solutions by immobilized laccase from Trametes versicolor

Energy Technology Data Exchange (ETDEWEB)

Catapane, Maria [Institute of Genetics and Biophysics “ABT”, Via P. Castellino, 111, 80131 Naples (Italy); National Institute of Biostructures and Biosystems (INBB), Viale Medaglie d’Oro, 305, 00136 Rome (Italy); Nicolucci, Carla; Menale, Ciro; Mita, Luigi [National Institute of Biostructures and Biosystems (INBB), Viale Medaglie d’Oro, 305, 00136 Rome (Italy); Department of Experimental Medicine, Second University of Naples, Via S. M. di Costantinopoli, 16, 80138 Naples (Italy); Rossi, Sergio [Institute of Genetics and Biophysics “ABT”, Via P. Castellino, 111, 80131 Naples (Italy); Mita, Damiano G., E-mail: mita@igb.cnr.it [Institute of Genetics and Biophysics “ABT”, Via P. Castellino, 111, 80131 Naples (Italy); National Institute of Biostructures and Biosystems (INBB), Viale Medaglie d’Oro, 305, 00136 Rome (Italy); Department of Experimental Medicine, Second University of Naples, Via S. M. di Costantinopoli, 16, 80138 Naples (Italy); Diano, Nadia [Institute of Genetics and Biophysics “ABT”, Via P. Castellino, 111, 80131 Naples (Italy); National Institute of Biostructures and Biosystems (INBB), Viale Medaglie d’Oro, 305, 00136 Rome (Italy); Department of Experimental Medicine, Second University of Naples, Via S. M. di Costantinopoli, 16, 80138 Naples (Italy)

2013-03-15

Highlights: ► Endocrine disruptors cause adverse effects in living organisms. ► Nonylphenol and Octylphenol are alkylphenols recognized as endocrine disruptors. ► It is necessary to remove or reduce their presence in the environment. ► Waters polluted by these pollutants have been bioremediated by immobilized laccase from Trametes versicolor. ► Laccase treated solutions were found to have lost any estrogenic activity. -- Abstract: A fluidized bed reactor, filled with laccase-based beads, has been employed to bioremediate aqueous solutions polluted by endocrine disruptors belonging to the alkylphenols (APs) class. In particular Octylphenol and Nonylphenol have been studied. The catalytic activity of free and immobilized laccase from Trametes versicolor has been characterized as a function of pH, temperature and substrate concentration in the reaction medium. In view of practical applications for each substrate concentration the removal efficiency (RE), the time to halve the initial concentration (τ{sub 50}), and the t{sub c=0}, i.e. the time to reach complete pollutant removal, have been calculated. The immobilized laccase exhibited a lower affinity for octylphenol (K{sub m} = 1.11 mM) than for Nonylphenol (K{sub m} = 0.72 mM), but all the other parameters of applicative interest resulted more significant for octylphenol. For example, the times to reach the complete removal of octylphenol compared to those for nonylphenol at the same concentration is shorter of about 15% (at low concentrations) up to 40% (at high concentrations). The study of cell proliferation with MPP89 cells, a human mesothelioma cell line, and the assay with the YES test indicated the loss of estrogenic activity of the APs solutions after laccase treatment.

Solute removal capacity of high cut-off membrane plasma separators.

Science.gov (United States)

Ohkubo, Atsushi; Kurashima, Naoki; Nakamura, Ayako; Miyamoto, Satoko; Iimori, Soichiro; Rai, Tatemitsu

2013-10-01

In vitro blood filtration was performed by a closed circuit using high cut-off membrane plasma separators, EVACURE EC-2A10 (EC-2A) and EVACURE EC-4A10 (EC-4A). Samples were obtained from sampling sites before the plasma separator, after each plasma separator, and from the ultrafiltrate of each separator. The sieving coefficient (S.C.) of total protein (TP), albumin (Alb), IgG, interleukin-6 (IL-6), interleukin-8 (IL-8), tumor necrosis factor-α (TNF-α), fibrinogen (Fib), antithrombin III (AT-III), and coagulation factor XIII (FXIII) were calculated. The S.C. of each solute using EC-2A and EC-A4 were as follows; TP: 0.25 and 0.56, Alb: 0.32 and 0.73, IgG: 0.16 and 0.50, IL-6:0.73 and 0.95, IL-8:0.85 and 0.82, TNF-α: 1.07 and 0.99, Fib: 0 and 0, FXIII: 0.07 and 0.17, respectively. When compared with the conventional type of membrane plasma separators, EVACURE could efficiently remove cytokines while retaining coagulation factors such as fibrinogen. Moreover, EC-2A prevented protein loss, whereas EC-4A could remove approximately 50% of IgG. © 2013 The Authors. Therapeutic Apheresis and Dialysis © 2013 International Society for Apheresis.

Application of a new adsorbent for fluoride removal from aqueous solutions

International Nuclear Information System (INIS)

Srivastav, Arun Lal; Singh, Prabhat K.; Srivastava, Varsha; Sharma, Yogesh C.

2013-01-01

Highlights: • A new adsorbent has been prepared. • The adsorbent is non-toxic and easy to synthesize. • HBO 1 has displayed best capacity for the removal of fluoride. • Unlike most adsorbents, HBO 1 is suitable for the removal of fluoride from water. • The process of removal has been optimized. -- Abstract: Hydrous bismuth oxides (HBOs) have been investigated as a possible adsorbent for fluoride removal from water. Apart from bismuth trioxide (Bi 2 O 3 ) compound, three additional HBOs, named as HBO 1 , HBO 2 , and HBO 3 were synthesized in the laboratory and examined for their relative potentials for fluoride removal from aqueous solutions. HBO 1 was observed to have highest fluoride removal at 10 mg/L initial concentration in aqueous environment. Among competitive anions, sulfate and chloride affect the fluoride removal by HBO 1 more adversely than bicarbonate. Characterization of HBOs using X-ray diffraction (XRD) pattern analyses indicated crystalline structures, and the broad chemical composition of materials showed successive increase of Bi(OH) 3 from HBO 1 to HBO 3 , with decrease of BiOCl in the same order. Fourier Transform Infrared (FTIR) spectroscopy analyses indicated presence of Bi-O bond and successively increasing number of peaks corresponding to OH ion from HBO 1 to HBO 3 . Scanning Electron Microscopic (SEM) images of HBOs show rough and porous structure of the materials. Presence of higher proportion of chloride compound in HBO 1 with respect to others appears to be the factor responsible for its better performance in fluoride removal from aqueous solutions

Efficiency Of Fabricated CNT-IPSFFe3O4 Nanocomposites In Removal Of Phenanthrenes From Contaminated Water

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Shisia K. Silvanus

2015-08-01

Full Text Available The increased demand for oil to supply the needs of industry and motorists has exposed the water sources to one of the greatest threats. The removal of selective organic pollutants such as phenanthrenes in aqueous solution was investigated by adsorption process on fabricated CNT-IPSFFe3O4 nanocomposites. Characterization of products confirmed the synthesis of individual nanomaterials in the nanocomposites. The SEM image of prepared CNTs showed configuration with abundant threadlike entities whose TEMs further confirmed evidence for formation of MWCNTs. The silica modified magnetite Fe3O4.SiO2 nanoparticles had clear distinct and spherical shaped nanoparticles arranged in a 2-D closed packed manner. The XRD diffraction pattern showed well crystalline magnetite silica NPs with particle size 22.4 nm from the Debye-Scherrer equation. The SEMEDAX analysis revealed large quantities of dispersive magnetite NPs with moderately uniform and cubic structures in the fabricated CNT-IPSFFe3O4 nanocomposites. Adsorption parameters were optimized at adsorbent dose 6 mg20ml contact time 40 mins pHPZC 4.5 and pH 5. Adsorption kinetics followed pseudo second order kinetics while the adsorption isotherm favored was Freundlich isotherms. The nanocomposites were not largely affected by of counter PAHs as its removal efficiency was 42.2 and 40.8 in the presence of naphthalene and anthracene respectively. This was replicated in its application in phenanthrenes removal from industrial wastewater in which the nanocomposites showed 63 phenanthrenes removal. The trend for the studied desorption solvents was acetone hexane methanol which had 47 42 and 22 removal efficiency respectively. The adsorption-desorption cycles involved a small volume of phenanthrene concentrates being recovered with gradual decrease in adsorption capacity for phenanthrene from 33.46 - 28.68 gg after three cycles. The desorption efficiency of phenanthrenes increased from to 49.81 to 56.98 wt

THIOGLYCOLIC ACID ESTERIFIED IN TO RICE STRAW FOR REMOVING LEAD FROM AQUEOUS SOLUTION

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R. Gong

2011-09-01

Full Text Available Thiol rice straw (TRS was prepared by esterifying thioglycolic acid onto rice straw in the medium of acetic anhydride and acetic acid with sulfuric acid as catalyst. The sorption of lead (Pb on TRS from aqueous solution was subsequently investigated. The batch experiments showed that Pb removal was dependent on initial pH, sorbent dose, Pb concentration, contact time, and temperature. The maximum value of Pb removal appeared at pH 5. For 100 mg/L of Pb solution, a removal ratio of greater than 98% could be achieved with 2.0 g/L or more of TRS. The isothermal data of Pb sorption conformed well to the Langmuir model, and the maximum sorption capacity (Qm of TRS for Pb was 104.17 mg/g. The equilibrium of Pb removal was reached within 120 min. The Pb removal process could be described by the pseudo-first-order kinetic model. The thermodynamic study indicated that the Pb removal process was spontaneous and endothermic.

Modeling the removal of Sunfix Red S3B from aqueous solution by electrocoagulation process using artificial neural network

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Manh Ha Bui

2016-01-01

Full Text Available This study presents an application of artificial neural networks (ANNs to predict the dye removal efficiency (color and chemical oxygen demand value of Electrocoagulation process from Sunfix Red S3B aqueous solution. The Bayesian regulation algorithm was applied to train the networks with experimental data including five factors: pH, current density, sulphate concentration, initial dye concentration (IDC, and electrolysis time. The predicting performance of the ANN models was validated through the low root mean square error value (9.844 %, mean absolute percentage error (13.776 % and the high determination coefficient value (0.836. Garson, Connection weight method and neural interpretation diagram were also used to study the influence of input variables on dye removal efficiency. For decolorization, the most effective inputs are determined as current density, electrolysis time and initial pH, while COD removal is found to be strongly affected by initial dye concentration and sulphate concentration. Through these steps, we demonstrated ANN’s robustness in modeling and analysis of electrocoagulation process.

Removal of phosphate and nitrate from aqueous solution using ...

African Journals Online (AJOL)

The aim of the present study was the removal of phosphate and nitrate by sodium alginate seagrass (Cymodocea rotundata) beads from aqueous solutions. The adsorption characteristics of phosphate and nitrate on the seagrass beads were optimized under different operational parameters like adsorbent dosage, initial ...

Application of Sargassum biomass to remove heavy metal ions from synthetic multi-metal solutions and urban storm water runoff.

Science.gov (United States)

Vijayaraghavan, K; Teo, Ting Ting; Balasubramanian, R; Joshi, Umid Man

2009-05-30

The ability of Sargassum sp. to biosorb four metal ions, namely lead, copper, zinc, and manganese from a synthetic multi-solute system and real storm water runoff has been investigated for the first time. Experiments on synthetic multi-solute systems revealed that Sargassum performed well in the biosorption of all four metal ions, with preference towards Pb, followed by Cu, Zn, and Mn. The solution pH strongly affected the metal biosorption, with pH 6 being identified as the optimal condition for achieving maximum biosorption. Experiments at different biosorbent dosages revealed that good biosorption capacity as well as high metal removal efficiency was observed at 3g/L. The biosorption kinetics was found to be fast with equilibrium being attained within 50 min. According to the Langmuir isotherm model, Sargassum exhibited maximum uptakes of 214, 67.5, 24.2 and 20.2mg/g for lead, copper, zinc, and manganese, respectively in single-solute systems. In multi-metal systems, strong competition between four metal ions in terms of occupancy binding sites was observed, and Sargassum showed preference in the order of Pb>Cu>Zn>Mn. The application of Sargassum to remove four heavy metal ions in real storm water runoff revealed that the biomass was capable of removing the heavy metal ions. However, the biosorption performance was slightly lower compared to that of synthetic metal solutions. Several factors were responsible for this difference, and the most important factor is the presence of other contaminants such as anions, organics, and other trace metals in the runoff.

Self-assembly modified-mushroom nanocomposite for rapid removal of hexavalent chromium from aqueous solution with bubbling fluidized bed.

Science.gov (United States)

Xu, Fei; Liu, Xu; Chen, Yijiao; Zhang, Ke; Xu, Heng

2016-05-18

A self-assembled modified Pleurotus Cornucopiae material (SMPM) combined with improved Intermittent Bubbling Fluidized Bed (IBFB) was investigated to remove the hexavalent chromium ions in aqueous solution. After the modification, the powder-like raw material gradually self-assembled together to SMPM, which had crinkly porous structure, improved the Cr-accommodation ability in a sound manner. Optimized by Taguchi method, Cr(VI) removal efficiency was up to 75.91% and 48.01% for 100 mg/L and 500 mg/L initial concentration of Cr(VI), respectively. Results indicated that the metal removal was dependent on dosage of adsorbent, particle diameter and treatment time. The experimental data obtained from the biosorption process was successfully correlated with Freundlich isotherm model. Thermodynamic study indicated the endothermic nature of the process. The results confirmed that self-assembly modified Pleurotus Cornucopiae material could be applied for the removal of heavy metal from wastewater in continuous fluidized bed process.

Removal of COD from laundry wastewater by electrocoagulation/electroflotation

Energy Technology Data Exchange (ETDEWEB)

Wang, C.-T. [Department of Safety Health and Environmental Engineering, Chung Hwa University of Medical Technology, Tainan County, Hsien 717, Taiwan (China)], E-mail: ctwwang@mail.hwai.edu.tw; Chou, W.-L. [Department of Safety Health and Environmental Engineering and Institute of Occupational Safety and Hazard Prevention, HungKuang University, Sha-Lu, Taichung 433, Taiwan (China); Kuo, Y.-M. [Department of Safety Health and Environmental Engineering, Chung Hwa University of Medical Technology, Tainan County, Hsien 717, Taiwan (China)

2009-05-15

The removal efficiency of COD in the treatment of simulated laundry wastewater using electrocoagulation/electroflotation technology is described. The experimental results showed that the removal efficiency was better, reaching to about 62%, when applying ultrasound to the electrocoagulation cell. The solution pH approached neutrality in all experimental runs. The optimal removal efficiency of COD was obtained by using the applied voltage of 5 V when considering the energy efficiency and the acceptable removal efficiency simultaneously. The Cl{sup -} concentration of less than 2500 ppm had a positive effect on the removal efficiency. The performance of the monopolar connection of electrodes was better than that of the bipolar connection in this work. In addition, the removal efficiency of using Al electrodes was higher in comparison with using Fe electrodes in the study. The highest COD removal amount per joule was found to be 999 mg dm{sup -3} kW h{sup -1} while using two Al electrodes, although the removal efficiency increased with the number of Al plates.

Magnetic nanoparticle (Fe3O4) impregnated onto tea waste for the removal of nickel(II) from aqueous solution

International Nuclear Information System (INIS)

Panneerselvam, P.; Morad, Norhashimah; Tan, Kah Aik

2011-01-01

The removal of Ni(II) from aqueous solution by magnetic nanoparticles prepared and impregnated onto tea waste (Fe 3 O 4 -TW) from agriculture biomass was investigated. Magnetic nanoparticles (Fe 3 O 4 ) were prepared by chemical precipitation of a Fe 2+ and Fe 3+ salts from aqueous solution by ammonia solution. These magnetic nanoparticles of the adsorbent Fe 3 O 4 were characterized by surface area (BET), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM) and Fourier Transform-Infrared Spectroscopy (FT-IR). The effects of various parameters, such as contact time, pH, concentration, adsorbent dosage and temperature were studied. The kinetics followed is first order in nature, and the value of rate constant was found to be 1.90 x 10 -2 min -1 at 100 mg L -1 and 303 K. Removal efficiency decreases from 99 to 87% by increasing the concentration of Ni(II) in solution from 50 to 100 mg L -1 . It was found that the adsorption of Ni(II) increases by increasing temperature from 303 to 323 K and the process is endothermic in nature. The adsorption isotherm data were fitted to Langmuir and Freundlich equation, and the Langmuir adsorption capacity, Q o , was found to be (38.3) mg g -1 . The results also revealed that nanoparticle impregnated onto tea waste from agriculture biomass, can be an attractive option for metal removal from industrial effluent.

Efficient removal of chromate and arsenate from individual and mixed system by malachite nanoparticles.

Science.gov (United States)

Saikia, Jiban; Saha, Bedabrata; Das, Gopal

2011-02-15

Malachite nanoparticles of 100-150 nm have been efficiently and for the first time used as an adsorbent for the removal of toxic arsenate and chromate. We report a high adsorption capacity for chromate and arsenate on malachite nanoparticle from both individual and mixed solution in pH ∼4-5. However, the adsorption efficiency decreases with the increase of solution pH. Batch studies revealed that initial pH, temperature, malachite nanoparticles dose and initial concentration of chromate and arsenate were important parameters for the adsorption process. Thermodynamic analysis showed that adsorption of chromate and arsenate on malachite nanoparticles is endothermic and spontaneous. The adsorption of these anions has also been investigated quantitatively with the help of adsorption kinetics, isotherm, and selectivity coefficient (K) analysis. The adsorption data for both chromate and arsenate were fitted well in Langmuir isotherm and preferentially followed the second order kinetics. The binding affinity of chromate is found to be slightly higher than arsenate in a competitive adsorption process which leads to the comparatively higher adsorption of chromate on malachite nanoparticles surface. Copyright © 2010 Elsevier B.V. All rights reserved.

Evaluation of ethylenediaminetetraacetic acid (EDTA) solution and gel for smear layer removal.

Science.gov (United States)

Dotto, Sidney Ricardo; Travassos, Rosana Maria Coelho; de Oliveira, Elias Pandonor Motcy; Machado, Manoel Eduardo de Lima; Martins, José Luiz

2007-08-01

The purpose of this in vitro study was to compare the efficacy of 24% ethylenediaminetetraacetic acid (EDTA) gel and 17% EDTA solution in cleaning dentine walls after root canal instrumentation. Thirty human canine teeth were divided into three groups of 10 teeth each. In Group 1, 1% sodium hypochlorite was used as the irrigating solution; in Group 2, 1% sodium hypochlorite was used with 17% EDTA solution; and in Group 3, 1% sodium hypochlorite was used with 24% EDTA gel. The presence of a smear layer was analysed after instrumentation using scanning electron microscopy. The Kruskal-Wallis test revealed a statistical difference (P 0.05). The results indicate that 1% sodium hypochlorite alone does not remove the smear layer and that there was no statistical difference between EDTA gel and EDTA solution in smear layer removal.

Investigation on the efficiency of treated Palm Tree waste for removal of organic pollutants

Science.gov (United States)

Azoulay, Karima; El HajjajiI, Souad; Dahchour, Abdelmalek

2017-04-01

Development of the industrial sector generates several problems of environmental pollution. This issue rises concern among scientific community and decision makers, in this work; we e interested in water resources polluted by the chemical substances, which can cause various problems of health. As an example, dyes generated by different industrial activities such as textile, cosmetic, metal plating, leather, paper and plastic sectors, constitute an important source of pollution. In this work, we aim at investigating the efficiency of palm tree waste for removal of dyes from polluted solution. Our work presents a double environmental aspect, on one hand it constitutes an attempt for valorization of Palm Tree waste, and on the other hand it provides natural adsorbent. The study focuses on the effectiveness of the waste in removing Methylene Bleu and Methyl Orange taken as models of pollutants from aqueous solution. Kinetics and isotherm experiments were conducted in order to determine the sorption behavior of the examined dye. The effects of initial dye and adsorbent concentrations are considered. The results indicate that the correlation coefficient calculated from pseudo-second order equation was higher than the other kinetic equations, indicating that equilibrium data fitted well with pseudo-second order model where adsorption process was chemisorption. The adsorption equilibrium was well described by Langmuir isotherm model.

Investigation of Cyanide Removal from Aqueous Solution Using Precipitation Process (FeCl3

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A. Jonidi Jafari

2013-02-01

Full Text Available Background and Objectives: Cyanide is a toxic pollutant that is can be discharged from different industries such as iron and steel industry, coal mining and metal plating. Presence of this toxin in water and wastewater is a serious hazard and lead to undesirable effects on both the environment and human. Thus, its concentration control is essential for human health. The aim of this study was investigation of Cyanide Removal from aqueous solution using precipitation process (FeCl3. Material and Methods: This study is an experimental study in lab scale that was carried out in a batch system by jartest. Variations of this study including pH, FeCl3 concentration, reaction time and desired concentration of cyanide were investigated. Data were analyzed using Excel (version 2007 software. Results: The results of this research were showed that Cyanide with initial concentration of 10 mg/l in precipitation process was removed by 40% (conditions pH=90, FeCl3=0.4 g/l and the time 60 minutes. Also, the precipitation process efficiency to cyanide removal decreased of 40 to 23%, by increasing of the initial cyanide concentration of 10 to 15 mg/l. Conclusion: Precipitation process can be considered as a suitable alternative for recovery of cyanide to be re-used. Although, this process has limitations for treat total cyanide to environmental standards level. So, it is better be used in combination with other processes of these contaminants removal.

Acetaldehyde Removal from Indoor Air through Chemical Absorption Using L-Cysteine

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Miyuki Noguchi

2010-09-01

Full Text Available The irreversible removal of acetaldehyde from indoor air via a chemical reaction with amino acids was investigated. To compare effectiveness, five types of amino acid (glycine, L-lysine, L-methionine, L-cysteine, and L-cystine were used as the reactants. First, acetaldehyde-laden air was introduced into aqueous solutions of each amino acid and the removal abilities were compared. Among the five amino acids, L-cysteine solution showed much higher removal efficiency, while the other amino acids solutions didn’t show any significant differences from the removal efficiency of water used as a control. Next, as a test of the removal abilities of acetaldehyde by semi-solid L-cysteine, a gel containing L-cysteine solution was put in a fluororesin bag filled with acetaldehyde gas, and the change of acetaldehyde concentration was measured. The L-cysteine-containing gel removed 80% of the acetaldehyde in the air within 24 hours. The removal ability likely depended on the unique reaction whereby acetaldehyde and L-cysteine rapidly produce 2-methylthiazolidine-4-carboxylic acid. These results suggested that the reaction between acetaldehyde and L-cysteine has possibilities for irreversibly removing toxic acetaldehyde from indoor air.

Biosorptive removal of cobalt (II) ions from aqueous solution by ...

African Journals Online (AJOL)

hope&shola

2010-11-29

Nov 29, 2010 ... chemical reaction, decay, adsorption and biodegradation. The presence of ... sted coffee (Dakiky et al., 2002), waste tea (Ahluwalia and Goyal, 2005) ..... green removal from aqueous solution by citric acid modified rice straw.

Highly efficient removal of pathogenic bacteria with magnetic graphene composite.

Science.gov (United States)

Zhan, Sihui; Zhu, Dandan; Ma, Shuanglong; Yu, Wenchao; Jia, Yanan; Li, Yi; Yu, Hongbing; Shen, Zhiqiang

2015-02-25

Magnetic Fe3O4/graphene composite (abbreviated as G-Fe3O4) was synthesized successfully by solvothermal method to effectively remove both bacteriophage and bacteria in water, which was tested by HRTEM, XRD, BET, XPS, FTIR, CV, magnetic property and zeta-potential measurements. Based on the result of HRTEM, the single-sheet structure of graphene oxide and the monodisperse Fe3O4 nanoparticles on the surface of graphene can be observed obviously. The G-Fe3O4 composite were attractive for removing a wide range of pathogens including not only bacteriophage ms2, but also various bacteria such as S. aureus, E. coli, Salmonella, E. Faecium, E. faecalis, and Shigella. The removal efficiency of E. coli for G-Fe3O4 composite can achieve 93.09%, whereas it is only 54.97% with pure Fe3O4 nanoparticles. Moreover, a detailed verification test of real water samples was conducted and the removal efficiency of bacteria in real water samples with G-Fe3O4 composite can also reach 94.8%.

Benzotriazole removal on post-Cu CMP cleaning

International Nuclear Information System (INIS)

Tang Jiying; Liu Yuling; Sun Ming; Fan Shiyan; Li Yan

2015-01-01

This work investigates systematically the effect of FA/O II chelating agent and FA/O I surfactant in alkaline cleaning solutions on benzotriazole (BTA) removal during post-Cu CMP cleaning in GLSI under the condition of static etching. The best detergent formulation for BTA removal can be determined by optimization of the experiments of single factor and compound cleaning solution, which has been further confirmed experimentally by contact angle (CA) measurements. The resulting solution with the best formulation has been measured for the actual production line, and the results demonstrate that the obtained cleaning solution can effectively and efficiently remove BTA, CuO and abrasive SiO 2 without basically causing interfacial corrosion. This work demonstrates the possibility of developing a simple, low-cost and environmentally-friendly cleaning solution to effectively solve the issues of BTA removal on post-Cu CMP cleaning in a multi-layered copper wafer. (paper)

Removal of Cr(VI) from Aqueous Environments Using Micelle-Clay Adsorption

Science.gov (United States)

Qurie, Mohannad; Khamis, Mustafa; Manassra, Adnan; Ayyad, Ibrahim; Nir, Shlomo; Scrano, Laura; Bufo, Sabino A.; Karaman, Rafik

2013-01-01

Removal of Cr(VI) from aqueous solutions under different conditions was investigated using either clay (montmorillonite) or micelle-clay complex, the last obtained by adsorbing critical micelle concentration of octadecyltrimethylammonium ions onto montmorillonite. Batch experiments showed the effects of contact time, adsorbent dosage, and pH on the removal efficiency of Cr(VI) from aqueous solutions. Langmuir adsorption isotherm fitted the experimental data giving significant results. Filtration experiments using columns filled with micelle-clay complex mixed with sand were performed to assess Cr(VI) removal efficiency under continuous flow at different pH values. The micelle-clay complex used in this study was capable of removing Cr(VI) from aqueous solutions without any prior acidification of the sample. Results demonstrated that the removal effectiveness reached nearly 100% when using optimal conditions for both batch and continuous flow techniques. PMID:24222757

Application of X-ray scanning and tomography to evaluate the filtercake removal efficiency

International Nuclear Information System (INIS)

Lopes, R.T.; Oliveira, L.F. de; Miranda, C.R.; Leite, J.C.

2004-01-01

The removal of the filtercake formed during the drilling operation is essential for a successful cementing job. Nowadays, the use of synthetic base fluids brings the necessity of proceeding new evaluations of the efficiency of the washes in removing the filtercake and to guarantee the wettability inversion of the formation from oil to waterwet. It is presented here the application of X-ray tomographic scanning to evaluate the filtercake removal efficiency performed by different washes. This technique uses a natural core with a perforation, where a filtercake is formed by circulating a drilling fluid. The wash is circulated through this perforation and the filtercake removal efficiency is measured precisely by computer tomography scanning. This procedure enables the filtercake removal visualization during the wash circulation through the formation and from the data obtained from the X-ray tomography it is possible to select the most appropriate wash for a given drilling fluid, as well as to predict the necessary contact time between the wash and the formation to achieve an appropriate filtercake removal

Toluene removal by oxidation reaction in spray wet scrubber: experimental, modeling and optimization

Directory of Open Access Journals (Sweden)

Roumporn Nikom

2006-11-01

Full Text Available Toluene, an important volatile organic compound (VOC, is used in many kinds of industries, such as painting, printing, coating, and petrochemical industries. The emission of toluene causes serious air pollution, odor problem, flammability problem and affects human health. This paper proposes the removal of toluene from waste air using a spray wet scrubber combining the absorption and oxidation reaction. Aqueous sodium hypochlorite (NaOCl solution was used as the scrubbing liquid in the system. NaOCl, the strongest oxidative agent, presents an effective toluene removal. As the scrubbed toluene is reacted, recirculation of the scrubbing liquid could be operated with a constant removal efficiency throughout the operting time. The investigated variables affecting the removal efficiency were air flow rate, inlet toluene concentration, NaOCl concentration, scrubbing liquid flow rate and size of spray nozzle. Influence of the scrubbing parameters was experimentally studied to develop a mathematical model of the toluene removal efficiency. The removal model reveals that the increase of scrubbing liquid flow rate, toluene concentration, and NaOCl concentration together with the decrease of air flow rate and size of spray nozzle can increase the toluene removal efficiency. Optimization problem with an objective function and constraints was set to provide the maximum toluene removal efficiency and solved by Matlab optimization toolbox. The optimization constraints were formed from the mathematical model and process limitation. The solution of the optimization was an air flow rate of 100 m3/h, toluene concentration of 1500 ppm, NaOCl concentration of 0.02 mol/l, NaOCl solution feed rate of 0.8 m3/h, and spray nozzle size of 0.5 mm. Solution of the optimization gave the highest toluene removal efficiency of 91.7%.

Efficient removal of trace antimony(III) through adsorption by hematite modified magnetic nanoparticles

International Nuclear Information System (INIS)

Shan, Chao; Ma, Zhiyao; Tong, Meiping

2014-01-01

Graphical abstract: - Highlights: • Sb(III) adsorption capacity of MNP@hematite was twice that of commercial Fe 3 O 4 . • pH, ionic strength, coexisting anions and NOM did not inhibit Sb(III) removal. • MNP@hematite could remove trace Sb(III) and As(III) from water simultaneously. • Efficient removal of Sb(III) from real tap water was achieved. • MNP@hematite could be easily recycled with a magnet and could be used repeatedly. - Abstract: Hematite coated magnetic nanoparticle (MNP@hematite) was fabricated through heterogeneous nucleation technique and used to remove trace Sb(III) from water. Powder X-ray diffraction, transmission electron microscopy (TEM), and alternating gradient magnetometry were utilized to characterize the prepared adsorbent. TEM image showed that MNP@hematite particles were spherical with size of 10–30 nm. With saturation magnetization of 27.0 emu/g, MNP@hematite particles could be easily separated from water with a simple magnetic process in short time (5 min). At initial concentration of 110 μg/L, Sb(III) was rapidly decreased to below 5 μg/L by MNP@hematite in 10 min. Sb(III) adsorption capacity of MNP@hematite was 36.7 mg/g, which was almost twice that of commercial Fe 3 O 4 nanoparticles. The removal of trace Sb(III) was not obviously affected by solution pH (over a wide range from 3 to 11), ionic strength (up to 100 mM), coexisting anions (chloride, nitrate, sulfate, carbonate, silicate, and phosphate, up to 10 mM) and natural organic matters (humic acid and alginate, up to 8 mg/L as TOC). Moreover, MNP@hematite particles were able to remove Sb(III) and As(III) simultaneously. Trace Sb(III) could also be effectively removed from real tap water by MNP@hematite. The magnetic adsorbent could be recycled and used repeatedly

Efficient removal of trace antimony(III) through adsorption by hematite modified magnetic nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Shan, Chao; Ma, Zhiyao; Tong, Meiping, E-mail: tongmeiping@pku.edu.cn

2014-03-01

Graphical abstract: - Highlights: • Sb(III) adsorption capacity of MNP@hematite was twice that of commercial Fe{sub 3}O{sub 4}. • pH, ionic strength, coexisting anions and NOM did not inhibit Sb(III) removal. • MNP@hematite could remove trace Sb(III) and As(III) from water simultaneously. • Efficient removal of Sb(III) from real tap water was achieved. • MNP@hematite could be easily recycled with a magnet and could be used repeatedly. - Abstract: Hematite coated magnetic nanoparticle (MNP@hematite) was fabricated through heterogeneous nucleation technique and used to remove trace Sb(III) from water. Powder X-ray diffraction, transmission electron microscopy (TEM), and alternating gradient magnetometry were utilized to characterize the prepared adsorbent. TEM image showed that MNP@hematite particles were spherical with size of 10–30 nm. With saturation magnetization of 27.0 emu/g, MNP@hematite particles could be easily separated from water with a simple magnetic process in short time (5 min). At initial concentration of 110 μg/L, Sb(III) was rapidly decreased to below 5 μg/L by MNP@hematite in 10 min. Sb(III) adsorption capacity of MNP@hematite was 36.7 mg/g, which was almost twice that of commercial Fe{sub 3}O{sub 4} nanoparticles. The removal of trace Sb(III) was not obviously affected by solution pH (over a wide range from 3 to 11), ionic strength (up to 100 mM), coexisting anions (chloride, nitrate, sulfate, carbonate, silicate, and phosphate, up to 10 mM) and natural organic matters (humic acid and alginate, up to 8 mg/L as TOC). Moreover, MNP@hematite particles were able to remove Sb(III) and As(III) simultaneously. Trace Sb(III) could also be effectively removed from real tap water by MNP@hematite. The magnetic adsorbent could be recycled and used repeatedly.

Performance and mechanisms for the removal of phthalates and pharmaceuticals from aqueous solution by graphene-containing ceramic composite tubular membrane coupled with the simultaneous electrocoagulation and electrofiltration process.

Science.gov (United States)

Yang, Gordon C C; Chen, Ying-Chun; Yang, Hao-Xuan; Yen, Chia-Heng

2016-07-01

In this study, commonly detected emerging contaminants (ECs) in water, including di-n-butyl phthalate (DnBP), di(2-ethylhexyl) phthalate (DEHP), cephalexin (CLX), sulfamethoxazole (SMX) and caffeine (CAF), were selected as the target contaminants. A lab-prepared graphene-containing ceramic composite tubular membrane (TGCCM) coupled with the simultaneous electrocoagulation and electrofiltration process (EC/EF) in crossflow filtration mode was used to remove target contaminants in model solution. Meanwhile, a comparison of the removal efficiency was made among various tubular composite membranes reported, including carbon fibers/carbon/alumina composite tubular membrane (TCCACM), titania/alumina composite tubular membrane (TTACM) and alumina tubular membrane (TAM). The results of this study showed that the removal efficiencies for DnBP and DEHP were 99%, whereas 32-97% for cephalexin (CLX), sulfamethoxazole (SMX) and caffeine (CAF). In this work the mechanisms involved in removing target ECs were proposed and their roles in removing various ECs were also discussed. Further, two actual municipal wastewaters were treated to evaluate the applicability of the aforementioned treatment technology (i.e., TGCCM coupled with EC/EF) to various aqueous solutions in the real world. Copyright © 2016 Elsevier Ltd. All rights reserved.

Efficient Removal of Arsenic Using Magnetic Multi-Granule Nanoclusters

International Nuclear Information System (INIS)

Lee, Seungho; Cha, Jinmyung; Sim, Kyunjong; Lee, Jinkyu

2014-01-01

Magnetic multi-granule nanoclusters (MGNCs) were investigated as an inexpensive means to effectively remove arsenic from aqueous environment, particularly groundwater sources consumed by humans. Various size MGNCs were examined to determine both their capacity and efficiency for arsenic adsorption for different initial arsenic concentrations. The MGNCs showed highly efficient arsenic adsorption characteristics, thereby meeting the allowable safety limit of 10 μg/L (ppb), prescribed by the World Health Organization (WHO), and confirming that 0.4 g and 0.6 g of MGNCs were sufficient to remove 0.5 mg/L and 1.0 mg/L of arsenate (AsO 4 3- ) from water, respectively. Adsorption isotherm models for the MGNCs were used to estimate the adsorption parameters. They showed similar parameters for both the Langmuir and Sips models, confirming that the adsorption process in this work was active at a region of low arsenic concentration. The actual efficiency of arsenate removal was then tested against 1 L of artificial arsenic-contaminated groundwater with an arsenic concentration of 0.6 mg/L in the presence of competing ions. In this case, only 1.0 g of 100 nm MGNCs was sufficient to reduce the arsenic concentrations to below the WHO permissible safety limit for drinking water, without adjusting the pH or temperature, which is highly advantageous for practical field applications

Efficient Removal of Arsenic Using Magnetic Multi-Granule Nanoclusters

Energy Technology Data Exchange (ETDEWEB)

Lee, Seungho; Cha, Jinmyung; Sim, Kyunjong; Lee, Jinkyu [Seoul National Univ., Seoul (Korea, Republic of)

2014-02-15

Magnetic multi-granule nanoclusters (MGNCs) were investigated as an inexpensive means to effectively remove arsenic from aqueous environment, particularly groundwater sources consumed by humans. Various size MGNCs were examined to determine both their capacity and efficiency for arsenic adsorption for different initial arsenic concentrations. The MGNCs showed highly efficient arsenic adsorption characteristics, thereby meeting the allowable safety limit of 10 μg/L (ppb), prescribed by the World Health Organization (WHO), and confirming that 0.4 g and 0.6 g of MGNCs were sufficient to remove 0.5 mg/L and 1.0 mg/L of arsenate (AsO{sub 4}{sup 3-}) from water, respectively. Adsorption isotherm models for the MGNCs were used to estimate the adsorption parameters. They showed similar parameters for both the Langmuir and Sips models, confirming that the adsorption process in this work was active at a region of low arsenic concentration. The actual efficiency of arsenate removal was then tested against 1 L of artificial arsenic-contaminated groundwater with an arsenic concentration of 0.6 mg/L in the presence of competing ions. In this case, only 1.0 g of 100 nm MGNCs was sufficient to reduce the arsenic concentrations to below the WHO permissible safety limit for drinking water, without adjusting the pH or temperature, which is highly advantageous for practical field applications.

THE EFFICIENCY OF ELECTROCOAGULATION PROCESS USING ALUMINUM ELECTRODES IN REMOVAL OF HARDNESS FROM WATER

Directory of Open Access Journals (Sweden)

M. Malakootian ، N. Yousefi

2009-04-01

Full Text Available There are various techniques for removal of water hardness each with its own special advantages and disadvantages. Electrochemical or electrocoagulation method due to its simplicity has gained a great attention and is used for removal of various ions and organic matters. The aim of the present study was to investigate the efficiency of this technique in removal of water hardness under different conditions. This experimental study was performed using a pilot plant. The applied pilot was comprised of a reservoir containing aluminum sheet electrodes. The electrodes were connected as monopolar and a power supply was used for supplying direct electrical current. Drinking water of Kerman (southeast of Iran was used in the experiments. The efficiency of the system in three different pH, voltages and time intervals were determined. Results showed the efficiency of 95.6% for electrocoagulation technique in hardness removal. pH and electrical potential had direct effect on hardness removal in a way that the highest efficiency rate was obtained in pH=10.1, potential difference of 20 volt and detention time of 60 minutes. Considering the obtained efficiency in the present study, electrocoagulation technique may be suggested as an effective alternative technique in hardness removal.

Struvite Precipitation and Phosphorous Removal from Urine Synthetic Solution: Reaction Kinetic Study

Directory of Open Access Journals (Sweden)

Marwa Saied Shalaby

2015-03-01

Full Text Available Phosphorus, like oil, is a non-renewable resource that must be harvested from finite resources in the earth’s crust. An essential element for life, phosphorus is becoming increasingly scarce, contaminated, and difficult to extract. Struvite or magnesium ammonium phosphate (MgNH4PO4.6H2O is a white, crystalline phosphate mineral that can be used as a bio-available fertilizer. The main objective of this research is to indicate the most important operating parameters affecting struvite precipitation by means of chemical reaction kinetics. The present study explores struvite precipitation by chemical method under different starting molar ratios, pH and SSR. It is shown that an increase of starting Mg: PO4: NH4 with respect to magnesium (1.6:1:1 strongly influences the growth rate of struvite and so the efficiency of the phosphate removal. This was attributed to the effect of magnesium on the struvite solubility product and on the reached supersaturation Super Saturation Ratio at optimum starting molar ratio and pH. It was also shown, by using chemical precipitation method that the determined Super Saturation Ratio (SSR values of struvite, at 8, 8.5, 9, 9.5 and 10 are 1.314, 4.29, 8.89, 9.87 and 14.89 respectively are close to those presented in the literature for different origins of wastewater streams. The results show that SSR , pH, and starting molar ratio strongly influences the kinetics of precipitation and so phosphorous removal to reach 93% removal percent , 5.95 mg/lit as a minimum PO4 remained in solution, and 7.9 gm precipitated struvite from feed synthetic solution of 750 ml . The product was subjected to chemical analysis by means of EDIX-FTIR, SEM and XRD showing conformity with published literature. First-order kinetics was found to be sufficient to describe the rate data. The rates increased with increasing pH and so SSR and the apparent rate constants for the reaction were determined. © 2015 BCREC UNDIP. All rights reserved

Micelle swelling agent derived cavities for increasing hydrophobic organic compound removal efficiency by mesoporous micelle@silica hybrid materials

KAUST Repository

Shi, Yifeng

2012-06-01

Mesoporous micelle@silica hybrid materials with 2D hexagonal mesostructures were synthesized as reusable sorbents for hydrophobic organic compounds (HOCs) removal by a facile one-step aqueous solution synthesis using 3-(trimethoxysily)propyl-octadecyldimethyl-ammonium chloride (TPODAC) as a structure directing agent. The mesopores were generated by adding micelle swelling agent, 1,3,5-trimethyl benzene, during the synthesis and removing it afterward, which was demonstrated to greatly increase the HOC removal efficiency. In this material, TPODAC surfactant is directly anchored on the pore surface of mesoporous silica via SiOSi covalent bond after the synthesis due to its reactive Si(OCH 3) 3 head group, and thus makes the synthesized materials can be easily regenerated for reuse. The obtained materials show great potential in water treatment as pollutants sorbents. © 2011 Elsevier Inc. All rights reserved.

An experimental study on removal efficiency of bio-particles in an airtight decontamination chamber

Energy Technology Data Exchange (ETDEWEB)

Li, Yanju [School of Environment Science and Technology, Tianjin University, Tianjin (China); National Biological Protection Engineering Center, Tianjin (China); Hao, Limei; Wang, Shuang; Hou, Lili; Zhang, Jinming; Qi, Jiancheng [National Biological Protection Engineering Center, Tianjin (China)

2009-11-15

Many bacteria and viruses lead to global dissemination of respiratory diseases, such as SARS, influenza, tuberculosis, pneumonia and asthma, by clinging to particles and transmission through aerosol. In this paper, an experiment was conducted to investigate the removal efficiency of bio-particles when exposed to ventilation in an airtight decontamination chamber made of stainless steel. After the bio-particles (Serratia marcescens) exposure condition was established in the chamber, the bio-particles removal efficiency was investigated. And a comparison experiment was then conducted with polystyrene latex spheres (PSL) as general particles under the same environmental condition. The comparison results indicate that the removal efficiency of bio-particles is lower than that of PSL during the first 300 s, but both removal efficiencies reached 90% almost at the same time. Furthermore, the differences between bio-particles and PSL, the influence of bio-particle size, environmental velocity, temperature and relative humidity on bio-particle removal efficiency were analyzed and discussed comprehensively. These data could not only underpin future numerical simulations of bio-particles, but also give information to aid in decisions for decreasing the risk of bio-particles pollution in a microbe exposure environment. (author)

Benzotriazole removal on post-Cu CMP cleaning

Science.gov (United States)

Jiying, Tang; Yuling, Liu; Ming, Sun; Shiyan, Fan; Yan, Li

2015-06-01

This work investigates systematically the effect of FA/O II chelating agent and FA/O I surfactant in alkaline cleaning solutions on benzotriazole (BTA) removal during post-Cu CMP cleaning in GLSI under the condition of static etching. The best detergent formulation for BTA removal can be determined by optimization of the experiments of single factor and compound cleaning solution, which has been further confirmed experimentally by contact angle (CA) measurements. The resulting solution with the best formulation has been measured for the actual production line, and the results demonstrate that the obtained cleaning solution can effectively and efficiently remove BTA, CuO and abrasive SiO2 without basically causing interfacial corrosion. This work demonstrates the possibility of developing a simple, low-cost and environmentally-friendly cleaning solution to effectively solve the issues of BTA removal on post-Cu CMP cleaning in a multi-layered copper wafer. Project supported by the Major National Science and Technology Special Projects (No. 2009ZX02308).

Statistical estimate of mercury removal efficiencies for air pollution control devices of municipal solid waste incinerators.

Science.gov (United States)

Takahashi, Fumitake; Kida, Akiko; Shimaoka, Takayuki

2010-10-15

Although representative removal efficiencies of gaseous mercury for air pollution control devices (APCDs) are important to prepare more reliable atmospheric emission inventories of mercury, they have been still uncertain because they depend sensitively on many factors like the type of APCDs, gas temperature, and mercury speciation. In this study, representative removal efficiencies of gaseous mercury for several types of APCDs of municipal solid waste incineration (MSWI) were offered using a statistical method. 534 data of mercury removal efficiencies for APCDs used in MSWI were collected. APCDs were categorized as fixed-bed absorber (FA), wet scrubber (WS), electrostatic precipitator (ESP), and fabric filter (FF), and their hybrid systems. Data series of all APCD types had Gaussian log-normality. The average removal efficiency with a 95% confidence interval for each APCD was estimated. The FA, WS, and FF with carbon and/or dry sorbent injection systems had 75% to 82% average removal efficiencies. On the other hand, the ESP with/without dry sorbent injection had lower removal efficiencies of up to 22%. The type of dry sorbent injection in the FF system, dry or semi-dry, did not make more than 1% difference to the removal efficiency. The injection of activated carbon and carbon-containing fly ash in the FF system made less than 3% difference. Estimation errors of removal efficiency were especially high for the ESP. The national average of removal efficiency of APCDs in Japanese MSWI plants was estimated on the basis of incineration capacity. Owing to the replacement of old APCDs for dioxin control, the national average removal efficiency increased from 34.5% in 1991 to 92.5% in 2003. This resulted in an additional reduction of about 0.86Mg emission in 2003. Further study using the methodology in this study to other important emission sources like coal-fired power plants will contribute to better emission inventories. Copyright © 2010 Elsevier B.V. All rights

Facile functionalized of SBA-15 via a biomimetic coating and its application in efficient removal of uranium ions from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Gao, Jun-Kai [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China); School of Energy and Environmental Engineering, Hebei University of Technology, Tianjin 300401 (China); Hou, Li-An; Zhang, Guang-Hui [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China); Gu, Ping, E-mail: guping@tju.edu.cn [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China)

2015-04-09

Highlights: • Dopamine-functionalized SBA-15 (DMS) was developed via a biomimetic coating. • The modification approach was simple, facile and cost-effective. • The DMS was firstly used to remove U(VI) from aqueous solution. • Large adsorption capacity and rapid separation were obtained. - Abstract: A novel dopamine-functionalized mesoporous silica (DMS), synthesized by grafting dopamine onto a mesoporous molecular sieve (SBA-15), was developed as a sorbent to extract U(VI) from aqueous solution. The method used to modify SBA-15 was simple, facile and cost-effective. The DMS was characterized by SEM, TEM, XRD and BET, showing that the material had an ordered mesoporous structure and a large surface area. The effect of contact time, pH, ionic strength, temperature, and solid–liquid ratio on the sorption process was investigated. It was demonstrated that the adsorption of U(VI) by DMS was fast and that it can be described by the pseudo-second order-equation where the equilibrium time was 20 min. Additionally, the adsorption isotherm data were fitted well by the Langmuir model with the maximum adsorption capacity of DMS of 196 mg/g at pH 6.0. Furthermore, the influence of the K{sup +} and Na{sup +} concentrations and solid-to-liquid ratio on the sorption was very weak, and the values of the thermodynamic parameters revealed that the sorption process was exothermic and spontaneous. All the results suggested that the DMS could be used as an excellent adsorbent to remove U(VI) from aqueous solution.

An efficient venturi scrubber system to remove submicron particles in exhaust gas.

Science.gov (United States)

Tsai, Chuen-Jinn; Lin, Chia-Hung; Wang, Yu-Min; Hunag, Cheng-Hsiung; Li, Shou-Nan; Wu, Zong-Xue; Wang, Feng-Cai

2005-03-01

An efficient venturi scrubber system making use of heterogeneous nucleation and condensational growth of particles was designed and tested to remove fine particles from the exhaust of a local scrubber where residual SiH4 gas was abated and lots of fine SiO2 particles were generated. In front of the venturi scrubber, normal-temperature fine-water mist mixes with high-temperature exhaust gas to cool it to the saturation temperature, allowing submicron particles to grow into micron sizes. The grown particles are then scrubbed efficiently in the venturi scrubber. Test results show that the present venturi scrubber system is effective for removing submicron particles. For SiO2 particles greater than 0.1microm, the removal efficiency is greater than 80-90%, depending on particle concentration. The corresponding pressure drop is relatively low. For example, the pressure drop of the venturi scrubber is approximately 15.4 +/- 2.4 cm H2O when the liquid-to-gas ratio is 1.50 L/m3. A theoretical calculation has been conducted to simulate particle growth process and the removal efficiency of the venturi scrubber. The theoretical results agree with the experimental data reasonably well when SiO2 particle diameter is greater than 0.1 microm.

Removal of PM10 by Forests as a Nature-Based Solution for Air Quality Improvement in the Metropolitan City of Rome

Directory of Open Access Journals (Sweden)

Federica Marando

2016-07-01

Full Text Available Nature-based solutions have been identified by the European Union as being critical for the enhancement of environmental qualities in cities, where urban and peri-urban forests play a key role in air quality amelioration through pollutant removal. A remote sensing and geographic information system (GIS approach was applied to the Metropolitan City (MC of Rome to assess the seasonal particulate matter (PM10 removal capacity of evergreen (broadleaves and conifers and deciduous species. Moreover, a monetary evaluation of PM10 removal was performed on the basis of pollution externalities calculated for Europe. Deciduous broadleaves represent the most abundant tree functional group and also yielded the highest total annual PM10 deposition values (1769 Mg. By contrast, PM10 removal efficiency (Mg·ha−1 was 15%–22% higher in evergreen than in deciduous species. To assess the different removal capacity of the three functional groups in an area with homogeneous environmental conditions, a study case was performed in a peri-urban forest protected natural reserve (Castelporziano Presidential Estate. This study case highlighted the importance of deciduous species in summer and of evergreen communities as regards the annual PM10 removal balance. The monetary evaluation indicated that the overall PM10 removal value of the MC of Rome amounted to 161.78 million Euros. Our study lends further support to the crucial role played by nature-based solutions for human well-being in urban areas.

The applications of populus fiber in removal of Cr{sup (VI)} from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Li, Miaomiao; Gong, Yumei, E-mail: ymgong@dlpu.edu.cn; Lyu, Aichao; Liu, Yuanfa, E-mail: morning309@126.com; Zhang, Hong, E-mail: zhang_hong1234@sina.com

2016-10-15

Highlights: • A sorbent for heavy metal ions based on populus fibers is prepared by a green way. • The chromium adsorption on the sorbent accords with the pseudo-second-order kinetics. • The proposed adsorption involves static attraction and chelation by the sorbent on chromium. • The sorbent is expected to be applied in universal conditions. - Abstract: The surface modification of natural materials to be applied in removal of Cr{sup (VI)} from aqueous solutions has attracted much attention. A natural sorbent for Cr{sup (VI)} based on natural populus fibers (PF) is prepared by transforming the cyano groups (AN) in polyacrylonitriles (PAN) grafted from PF into amidoxime groups (AO), which has strong ability to attract and chelate heavy metal ions. The prepared sorbent is characterized by Fourier Transform Infrared Spectra (FT-IR), thermogravimetric analysis (TGA), solid-state nuclear magnetic resonance ({sup 13}C NMR) and scanning electron microscope (SEM). As potassium dichromate solution (K{sub 2}Cr{sub 2}O{sub 7}) is used as a target solution for detecting adsorption capacity of the sorbent, the adsorption kinetics of the sorbent for chromiun is consistent with the pseudo-second-order kinetic model by analyzing the adsorption amount as a function of the sorbent dispersed duration in solution at pH = 2. The expected adsorption mechanism is that the Cr{sup (VI)} in anionic ions Cr{sub 2}O{sub 7}{sup 2−} and HCrO{sub 4}{sup −} are adsorbed through electrostatic attraction but when Cr{sup (VI)} is reduced to Cr{sup (III)} by AO, the electronegative nitrogen and oxygen in AO chelate it through coordination bond. The as-prepared PF derivant with high adsorption efficiency of chromium 180.5 mg/g (3.47 mmol/g), low cost, reusability and greenly preparation process suggests that the development of natural PF as a sorbent in removal of Cr{sup (VI)} from aqueous solutions is a destined significant approach.

Tetrachloroethylene Removal Rate from Aqueous Solutions by Pumice Doped with Copper: An Evaluation of the Effect of pH

Directory of Open Access Journals (Sweden)

Ali Almasi

2016-12-01

Full Text Available Tetrachloroethylene (TCE is a chlorinated aliphatic hydrocarbon, used in many industries. Effective and efficient treatment of industrial wastewater, containing TCE, is one of the environmental requirements. The purpose of this study was to determine the role of alkaline environments in TCE removal rate from aqueous solutions, using copper-doped pumice. This experimental study was performed, using granulated pumice stones with a mesh 4 (8.4 mm in alkaline conditions; the samples were coated with copper. Copper-doped pumice was prepared as a bed at doses of 1, 2, and 3 g/L; the study was performed at pH ranges of 3, 7, and 11. Based on the results, copper-doped pumice showed good efficacy in TCE removal; in addition, its performance increased in alkaline conditions. Therefore, use of this stone for the treatment of wastewater, containing TCE, is effective due to its availability and low cost. Besides, it can be considered a good option, given its high efficiency in the absorption process.

Removal of metallic ions from aqueous solutions by fluidized bed fly ashes

Energy Technology Data Exchange (ETDEWEB)

Rio, S.; Delebarre, A.; Hequet, V. [Ecole des Mines de Nantes, 44 - Nantes (France); Blondin, J. [Cerchar 62 - Mazingarbe (France)

2001-07-01

One of the main constraints deriving from the generation of power by coal combustion is to find some use for the fly ashes instead of disposing of them. Fly ashes from two fluidized bed power plants were tested to remove Pb{sup 2+}, Cu{sup 2+}, Cr (III), Ni{sup 2+}, Zn{sup 2+} and Cr (VI) from aqueous solutions. Experimental design methodology was used to study the removal and the leaching as a function of (i) the water pollutant content, (ii) the metal concentration in water, (iii) the pH of the solution and (iv) the addition of lime to fly ashes. The results show that the percentage of adsorbed ions was more important when they were in contact with silico-aluminous fly ashes than sulfo-calcic fly ashes, except in the case of the ion Ni{sup 2+}. The removal of metallic ions increases with increasing pH. The metallic canons removal accounting for the leaching test was higher when lime was added to silico-aluminous fly ashes during the adsorption. (authors)

Functionalization of Microcrystalline Cellulose with N,N-dimethyldodecylamine for the Removal of Congo Red Dye from an Aqueous Solution

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Dongying Hu

2014-08-01

Full Text Available Microcrystalline cellulose (MCC was functionalized with quaternary amine groups for use as an adsorbent to remove Congo Red dye (CR from aqueous solution. The ultrasonic pretreatment of MCC was investigated during its functionalization. Characterization was conducted using infrared spectroscopy (FT-IR, X-ray photoelectron spectroscopy (XPS, X-ray diffraction (XRD, and scanning electron microscopy (SEM. The batch adsorption of the functionalized MCC was studied to evaluate the effects of dye concentration, pH of solution, temperature, and NaCl concentration on the adsorption CR. The adsorbent (FM-1 obtained using ultrasonic pretreatment of MCC under 10.8 kJ•g–1 exhibited an adsorption capacity of 304 mg•g–1 at initial pH under a dose of 0.1 g•L–1 and initial concentration of 80 mg•L–1. After functionalization, the FT-IR and XPS results indicated that the quaternary amine group was successfully grafted onto the cellulose, the surface was transformed to be coarse and porous, and the crystalline structure of the original cellulose was disrupted. FM-1 has been shown to be a promising and efficient adsorbent for the removal of CR from an aqueous solution.

Optimization of Photooxidative Removal of Phenazopyridine from Water

Science.gov (United States)

Saeid, Soudabeh; Behnajady, Mohammad A.; Tolvanen, Pasi; Salmi, Tapio

2018-05-01

The photooxidative removal of analgesic pharmaceutical compound phenazopyridine (PhP) from aqueous solutions by UV/H2O2 system with a re-circulated photoreactor was investigated. Response surface methodology (RSM) was employed to optimize the effect of operational parameters on the photooxidative removal efficiency. The investigated variables were: the initial PhP and H2O2 concentrations, irradiation time, volume of solution and pH. The analysis of variance (ANOVA) of quadratic model demonstrated that the described model was highly significant. The predicted values of the photooxidative removal efficiency were found to be in a fair agreement with experimental values ( R 2 = 0.9832, adjusted R 2 = 0.9716). The model predicted that the optimal reaction conditions for a maximum removal of PhP (>98%) were: initial PhP concentration less than 23 mg L-1, initial concentration of H2O2 higher than 470 mg L-1, solution volume less than 500 mL, pH close to 2 and irradiation time longer than 6 min.

Hydrocolloid-Stabilized Magnetite for Efficient Removal of Radioactive Phosphates

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Vinod Vellora Thekkae Padil

2014-01-01

Full Text Available Liquid radioactive waste is a common by-product when using radioactive isotopes in research and medicine. Efficient remediation of such liquid waste is crucial for increasing safety during the necessary storage of the material. Herein, we present a novel Gum Karaya stabilized magnetite for the efficient removal of radioactive phosphorus 32P from liquid radioactive waste. This environmentally friendly material is well suited to be used as a nanohydrogel for the removal of liquid waste, which can then be stored in a smaller space and without the risk of the spills inherent to the initial liquid material. The maximum adsorption capacity of the GK/M in this study was found to be 15.68 GBq/g. We present a thorough morphological characterization of the synthesised GK/M, as well as a discussion of the possible phosphorus adsorption mechanisms.

Removal of radium from aqueous solutions using adsorbent produced from coconut coir pith

International Nuclear Information System (INIS)

Zalina Laili; Muhamat Omar; Mohd Zaidi Ibrahim; Esther Phillip; Mohd Abdul Wahab Yusof; Hassan, A.

2008-08-01

A study was conducted to evaluate the potential use of the coconut coir pith as an adsorbent for the removal of radium from aqueous solutions. Experiments to establish adsorptions as a function of pH and contact time were carried out. The results showed that radium adsorption are dependent upon pH and contact time of coconut coir pith with aqueous solutions. 70-80% of radium were adsorbed in the neutral to alkaline pH range. The amount of radium adsorbed also increased with contact time, reaching an optimum after 250 min. Thus, it can be concluded that the coconut coir pith has the potential to be used as an adsorbent in radium removal from aqueous solutions. (Author)

Parametric study on removal efficiency of impregnated activated charcoal and silver zeolite for radioactive methyl iodide

International Nuclear Information System (INIS)

Shiomi, H.; Yuasa, Y.; Tani, A.; Ohki, M.; Nakagawa, T.

1983-01-01

The removal efficiency of impregnated activated charcoal and silver zeolite for radioactive methyl iodide is influenced by various parameters such as temperature, relative humidity, face velocity and packing density. This study is to evaluate the dependency of the removal efficiency on each parameter and these combined parameters, quantitatively. Four types of adsorbents, BC-727, AgX, CHC-50 and SS 208C 5KI 3 , were tested. From experimental data and mass transfer theory, an experimental equation for evaluating the removal efficiency of adsorbents was derived under a series of experiments for radioactive methyl iodine-131. It was concluded that the removal efficiency calculated from the experimental equation agreed well with the experimental value. Effects of experimental specific parameters, such as Pre-flow time, methyl iodide injection time and After-flow time, on the removal efficiency of adsorbent are also described

Removal of phosphate and nitrate from aqueous solution using ...

African Journals Online (AJOL)

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water, 3.5 g of NaCl were dissolved to obtain 3.5 g/l salinity final solution. When the ... The nitrate adsorption was highly pH dependent, which affects the ... adsorption mechanism that the optimum pH for phosphate removal by .... Biosorption of copper(ii) from aqueous ... Accumulation and detoxification of toxic elements by ...

Application of Electrocoagulation Process Using Iron and Aluminum Electrodes for Fluoride Removal from Aqueous Environment

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Edris Bazrafshan

2012-01-01

Full Text Available Fluoride in drinking water above permissible level is responsible for human being affected by skeletal fluorosis. The present study was carried out to assess the ability of electrocoagulation process with iron and aluminum electrodes in order to removal of fluoride from aqueous solutions. Several working parameters, such as fluoride concentration, pH, applied voltage and reaction time were studied to achieve a higher removal capacity. Variable concentrations (1, 5 and 10 mg L-1 of fluoride solutions were prepared by mixing proper amount of sodium fluoride with deionized water. The varying pH of the initial solution (3, 7 and 10 was also studied to measure their effects on the fluoride removal efficiency. Results obtained with synthetic solution revealed that the most effective removal capacities of fluoride could be achieved at 40 V electrical potential. In addition, the increase of electrical potential, in the range of 10-40 V, enhanced the treatment rate. Also comparison of fluoride removal efficiency showed that removal efficiency is similar with iron and aluminum electrodes. Finally it can be concluded that the electrocoagulation process has the potential to be utilized for the cost-effective removal of fluoride from water and wastewater.

Antibiotic resistance genes fate and removal by a technological treatment solution for water reuse in agriculture.

Science.gov (United States)

Luprano, Maria Laura; De Sanctis, Marco; Del Moro, Guido; Di Iaconi, Claudio; Lopez, Antonio; Levantesi, Caterina

2016-11-15

In order to mitigate the potential effects on the human health which are associated to the use of treated wastewater in agriculture, antibiotic resistance genes (ARGs) are required to be carefully monitored in wastewater reuse processes and their spread should be prevented by the development of efficient treatment technologies. Objective of this study was the assessment of ARGs reduction efficiencies of a novel technological treatment solution for agricultural reuse of municipal wastewaters. The proposed solution comprises an advanced biological treatment (Sequencing Batch Biofilter Granular Reactor, SBBGR), analysed both al laboratory and pilot scale, followed by sand filtration and two different disinfection final stages: ultraviolet light (UV) radiation and peracetic acid (PAA) treatments. By Polymerase Chain Reaction (PCR), the presence of 9 ARGs (ampC, mecA, ermB, sul1, sul2, tetA, tetO, tetW, vanA) were analysed and by quantitative PCR (qPCR) their removal was determined. The obtained results were compared to the reduction of total bacteria (16S rDNA gene) and of a faecal contamination indicator (Escherichia coli uidA gene). Only four of the analysed genes (ermB, sul1, sul2, tetA) were detected in raw wastewater and their abundance was estimated to be 3.4±0.7 x10(4) - 9.6±0.5 x10(9) and 1.0±0.3 x10(3) to 3.0±0.1 x10(7) gene copies/mL in raw and treated wastewaters, respectively. The results show that SBBGR technology is promising for the reduction of ARGs, achieving stable removal performance ranging from 1.0±0.4 to 2.8±0.7 log units, which is comparable to or higher than that reported for conventional activated sludge treatments. No reduction of the ARGs amount normalized to the total bacteria content (16S rDNA), was instead obtained, indicating that these genes are removed together with total bacteria and not specifically eliminated. Enhanced ARGs removal was obtained by sand filtration, while no reduction was achieved by both UV and PAA disinfection

Membrane Characteristics for Removing Particulates in PFC Wastes

International Nuclear Information System (INIS)

Kim, Gye Nam; Lee, Sung Yeol; Won, Hui Jun; Jung, Chong Hun; Oh, Won Zin; Park, Jin Ho

2005-01-01

Pc (Per fluorocarbon) decontamination process is one of best methods to remove hot particulate adhered at inside surface of hot cell and surface of equipment in hot cell. It was necessary to develop a particulate filtration equipment to reuse Pc solution used on Pc decontamination due to its high cost and to minimize the volume of second wastewater. Contamination characteristics of hot particulate were investigated and then a filtration process was presented to remove hot particulate in Pc solution generated through Pc decontamination process. The removal efficiency of Pvdf (Poly vinylidene fluoride), Pp (Polypropylene), Ceramic (Al 2 O 3 ) filter showed more than 95%. The removal efficiency of Pvdf filter was a little lower than those of other kiters at same pressure (3 psi). A ceramic filter showed a higher removal efficiency with other filters, while a little lower flux rate than other filters. Due to inorganic composition, a ceramic filter was highly stable against radio nuclides in comparison with Pvdf and Pp membrane, which generate H 2 gas in α-radioactivity atmosphere. Therefore, the adoption of ceramic filter is estimated to be suitable for the real nitration process.

Natural organic matters removal efficiency by coagulation

Science.gov (United States)

Sapingi, Mohd Sharizal Mohd; Pishal, Munirah; Murshed, Mohamad Fared

2017-10-01

The presence of Natural Organic Matter (NOM) in surface water results in unwanted characteristics in terms of color, odor, and taste. NOM content reaction with free chlorine in treated water lowers the water quality further. Chlorine is added for disinfection and produces undesirable disinfection by-products (DPBs). DBPs in drinking water are carcinogenic to consumers and may promote cancerous cell development in the human body. This study was performed to compare the coagulant efficiency of aluminum sulfate (Alum) and ferric chloride (FeCl3) on NOM removal (as in UV254 absorbance) and turbidity removal under three pH conditions (pH 6, pH 7, and sample actual pH). The three sampling points for these studies were Jalan Baru River, Kerian River, and Redac Pond. Additional sampling points, such as Lubuk Buntar and a tubewell located in the Civil Engineering School, were included to observe differences in characteristics. DOC, UV absorbance, and full wavelength were tested, after which samples treated with alum were also tested to further analyze the NOM content. Based on UV254 absorbance and DOC data, specific UV value was calculated to obtain vital synopsis of the characteristics of NOM content, as well as coagulation efficiency.

Removal efficiency of water purifier and adsorbent for iodine, cesium, strontium, barium and zirconium in drinking water.

Science.gov (United States)

Sato, Itaru; Kudo, Hiroaki; Tsuda, Shuji

2011-01-01

The severe incident of Fukushima Daiichi Nuclear Power Station has caused radioactive contamination of environment including drinking water. Radioactive iodine, cesium, strontium, barium and zirconium are hazardous fission products because of the high yield and/or relatively long half-life. In the present study, 4 pot-type water purifiers and several adsorbents were examined for the removal effects on these elements from drinking water. Iodide, iodate, cesium and barium were removed by all water purifiers with efficiencies about 85%, 40%, 75-90% and higher than 85%, respectively. These efficiencies lasted for 200 l, which is near the recommended limits for use of filter cartridges, without decay. Strontium was removed with initial efficiencies from 70% to 100%, but the efficiencies were slightly decreased by use. Zirconium was removed by two models, but hardly removed by the other models. Synthetic zeolite A4 efficiently removed cesium, strontium and barium, but had no effect on iodine and zirconium. Natural zeolite, mordenite, removed cesium with an efficiency as high as zeolite A4, but the removal efficiencies for strontium and barium were far less than those of zeolite A4. Activated carbon had little removal effects on these elements. In case of radioactive contamination of tap water, water purifiers may be available for convenient decontamination of drinking water in the home.

Removal of heavy metals from aqueous solution by Carrot residues

International Nuclear Information System (INIS)

Eslamzadeh, T.; Nasernejad, B.; Bonakdar Pour, B.; Zamani, A.; Esmaail-Beygi, M.

2004-01-01

The removal of Copper(II), Zinc(II), and Chromium (III) from wastewater by carrot residues was investigated to evaluate cation exchange capacity. The effects of solution P H and co-ions were studied in batch experiments. Adsorption equilibria were initially rapidly established, and then decreased markedly after 10 min. Column experiments were carried out in a glass column filled with carrot residues to evaluate the metal removal capacity. The influences of the feed concentration and feed rate were also studied in order to compare the dynamic capacity for metal binding in different feed concentrations

[Efficiency of photodecomposition of trace NDMA in water by UV irradiation].

Science.gov (United States)

Xu, Bing-Bing; Chen, Zhong-Lin; Qi, Fei; Ma, Jun

2008-07-01

Efficiency of photodecomposition of trace NDMA by UV irradiation was investigated with analyzing the initial concentration of NDMA, solution pH, irradiation area, irradiation intensity and water quality effect on NDMA photolysis. NDMA could be effectively photodegraded by UV irradiation. The removal efficiency of NDMA was 97.5% after 5 min of UV irradiation. Effect of initial NDMA concentration on photodecomposition of NDMA was not remarkable. With pH value ascending, the removal rate of NDMA photodecomposition decreased. The yields of photoquantum were more under lower solution pH than that under higher pH. NDMA had fastest reaction rate at solution pH = 2.2. Removal efficiency of NDMA increased with the available irradiation area ascending. Increscent ultraviolet irradiation intensity was good for NDMA degradation. Water quality affected the removal of NDMA slightly. The removal efficiency of NDMA in tap water and Songhua River raw water were 96.7% and 94.8%, respectively.

A study on nitrogen removal efficiency of Pseudomonas stutzeri ...

African Journals Online (AJOL)

USER

2010-02-08

Feb 8, 2010 ... ambient temperature in the reaction system, the efficiency of nitrogen removal was studied. The results ... no reported experiment which has been conducted to ... controlled shaker at 32°C with a 150 r/min rotating speed (Ahn,.

Indian jujuba seed powder as an eco-friendly and a low-cost biosorbent for removal of acid blue 25 from aqueous solution.

Science.gov (United States)

Krishna, L Sivarama; Reddy, A Sreenath; Zuhairi, W Y Wan; Taha, M R; Reddy, A Varada

2014-01-01

Indian jujuba seed powder (IJSP) has been investigated as a low-cost and an eco-friendly biosorbent, prepared for the removal of Acid Blue 25 (AB25) from aqueous solution. The prepared biomaterial was characterized by using FTIR and scanning electron microscopic studies. The effect of operation variables, such as IJSP dosage, contact time, concentration, pH, and temperature on the removal of AB25 was investigated, using batch biosorption technique. Removal efficiency increased with increase of IJSP dosage but decreased with increase of temperature. The equilibrium data were analyzed by the Langmuir and the Freundlich isotherm models. The data fitted well with the Langmuir model with a maximum biosorption capacity of 54.95 mg g(-1). The pseudo-second-order kinetics was the best for the biosorption of AB25 by IJSP, with good correlation. Thermodynamic parameters such as standard free energy change (ΔG(0)), standard enthalpy changes (ΔH(0)), and standard entropy changes (ΔS(0)) were analyzed. The removal of AB25 from aqueous solution by IJSP was a spontaneous and exothermic adsorption process. The results suggest that IJSP is a potential low-cost and an eco-friendly biosorbent for the AB25 removal from synthetic AB25 wastewater.

Zero-valent iron particles embedded on the mesoporous silica–carbon for chromium (VI) removal from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Xiong, Kun, E-mail: kunxiong312@gmail.com; Gao, Yuan [Chongqing Technology and Business University, Engineering Research Center for Waste Oil Recovery Technology and Equipment of Ministry of Education, Chongqing Key Laboratory of Catalysis & Environmental New Materials (China); Zhou, Lin [Chengdu Radio and TV University (China); Zhang, Xianming [Chongqing Technology and Business University, Engineering Research Center for Waste Oil Recovery Technology and Equipment of Ministry of Education, Chongqing Key Laboratory of Catalysis & Environmental New Materials (China)

2016-09-15

Nanoscale zero-valent iron (nZVI) particles were embedded on the walls of mesoporous silica–carbon (MSC) under the conditions of high-temperature carbonization and reduction and used to remove chromium (VI) from aqueous solution. The structure and textural properties of nZVI–MSC were characterized by the powder X-ray diffraction, transmission electron microscopy and N{sub 2} adsorption and desorption. The results show that nZVI–MSC has highly ordered mesoporous structure and large surface area, indistinguishable with that of MSC. Compared with the support MSC and iron particles supported on the activated carbon (nZVI/AC), nZVI–MSC exhibited much higher Cr(VI) removal efficiency with about 98 %. The removal process obeys a pseudo first-order model. Such excellent performance of nZVI–MSC could be ascribed to the large surface and iron particles embedded on the walls of the MSC, forming an intimate contact with the MSC. It is proposed that this feature might create certain micro-electrode on the interface of iron particles and MSC, which prevented the formation of metal oxide on the surface and provided fresh Fe surface for Cr(VI) removal.

Removal of radioactive cesium from soil by ammonium citrate solution and ionic liquid

International Nuclear Information System (INIS)

Ishiwata, Shunji; Kitakouji, Manabu; Taga, Atsushi; Ogata, Fumihiko; Ouchi, Hidekazu; Yamanishi, Hirokuni; Inagaki, Masayo

2015-01-01

Radioactive cesium has strongly bound soil as time proceeded, which could not be cleaved in mild condition. We have found that serial treatment of ammonium citrate solution and ionic liquid removed radioactive cesium from soil effectively. The sequence of the treatment is crucial, since inverse serial treatment or mixture of two kinds of solution did not show such an effect, which suggested that ammonium citrate unlocked trapped cesium in soil and ionic liquid solved it. We also found that repeating serial treatment and prolonged treatment time additively removed cesium from soil. (author)

Poly(acrylamide) functionalized chitosan: An efficient adsorbent for azo dyes from aqueous solutions

International Nuclear Information System (INIS)

Singh, Vandana; Sharma, Ajit Kumar; Sanghi, Rashmi

2009-01-01

In the present communication we report on the optimization of persulfate/ascorbic acid initiated synthesis of chitosan-graft-poly(acrylamide) (Ch-g-PAM) and its application in the removal of azo dyes. The optimum yield of the copolymer was obtained using 16 x 10 -2 M acrylamide, 3.0 x 10 -2 M ascorbic acid, 2.4 x 10 -3 M K 2 S 2 O 8 and 0.1 g chitosan in 25 mL of 5% aqueous formic acid at 45 ± 0.2 o C. Ch-g-PAM remained water insoluble even under highly acidic conditions and could efficiently remove Remazol violet and Procion yellow dyes from the aqueous solutions over a pH range of 3-8 in contrast to chitosan (Ch) which showed pH dependent adsorption. The adsorption data of the Ch-g-PAM and Ch for both the dyes were modeled by Langmuir and Freundlich isotherms where the data fitted better to Langmuir isotherms. To understand the adsorption behavior of Ch-g-PAM, adsorption of Remazol violet on to the copolymer was optimized and the kinetic and thermodynamic studies were carried out taking Ch as reference. Both Ch-g-PAM and Ch followed pseudo-second-order adsorption kinetics. The thermodynamic study revealed a positive heat of adsorption (ΔH o ), a positive ΔS o and a negative ΔG o , indicating spontaneous and endothermic nature of the adsorption of RV dye on to the Ch-g-PAM. The Ch-g-PAM was found to be very efficient in removing color from real industrial wastewater as well, though the interfering ions present in the wastewater slightly hindered its adsorption capacity. The data from regeneration efficiencies for ten cycles evidenced the high reusability of the copolymer in the treatment of waste water laden with even high concentrations of dye.

Study of RBC Efficiency in Aniline Removal by Increasing Contactor Specific Surface

Directory of Open Access Journals (Sweden)

Seyed Hossein Mousavi Aliani

2011-01-01

Full Text Available Aniline is a first type amino aromatic compound and has various applications in different pharmaceutical, synthetic dye, plastic, and petrochemical industries. It is poisonous and its discharge into the environment causes serious hazards that warrant it removal by an efficient treatment process.  In this study, the efficiency of rotating biological contactors in aniline removal was investigated using four 3-liter parallel systems (in two series. Two reactors in the first series had 27 disks. The second series had 14 discs with packings in each reactor with the same specific surfaces as compared to the first system.Aniline concentrations from 100 to 1200 mg/L and hydraulic loading rates from 1.57 to 6.28 L/m2.d were used throughout the study period in two treatments. The effect of disc rotation speed on system efficiency was also investigated. The results indicated that COD removal efficiency decreased with increasing hydraulic loading rate but increased with increasing disc speed from 5 to 15 rpm. The best removal efficiencies of 88 and 86 percent for RBCI and RBCII, respectively, were obtained for an aniline concentration of 400 mg/L, a hydraulic loading rate of 1.57 L/m2.d, and a disc speed of 15 rpm. Based on the results, although both systems yield almost equal efficiencies, the start-up period was shorter in RBCII with a clearer effluent due to the lower quantity of suspended microorganisms in the reactor than that in RBCI. Use of packing may decrease energy consumption for disc rotation due to the overall weight reduction of the system.

Using quartz sand to enhance the removal efficiency of M. aeruginosa by inorganic coagulant and achieve satisfactory settling efficiency.

Science.gov (United States)

Pei, Haiyan; Jin, Yan; Xu, Hangzhou; Ma, Chunxia; Sun, Jiongming; Li, Hongmin

2017-10-19

In this study, low-cost and non-polluting quartz sand was respectively mixed with AlCl 3 , FeCl 3 and PAFC to synergistically remove Microcystis aeruginosa. Results showed that quartz sand could markedly increase the algae removal efficiency and decrease the coagulant doses. The increase of removal efficiency with AlCl 3 and FeCl 3 was only due to the enhancement of floc density by the quartz sand. However, the removal efficiency with PAFC was increased not only by the enhanced floc density, but also by the enlarged floc size. Flocs from 50 mg/L sand addition were larger than that with other sand doses, which was on account of the appropriate enhancement of collision efficiency at this dose. After coagulation, the extracellular organic matter (EOM) and microcystins (MCs) in system with quartz sand was remarkably reduced. That's because quartz sand can enhance the coagulation so as to improve capping the EOM and MCs in flocs during coagulation process. Owing to 200 mg/L quartz sand could damage the cell's membrane during coagulation proces, algal cells in the system lysed two days earlier than with 50 mg/L sand during flocs storage. In addition, cells with PAFC incurred relatively moderate cellular oxidative damage and could remain intact for longer time.

Removal of Cr6 + and Ni2+ from aqueous solution using bagasse and fly ash.

Science.gov (United States)

Rao, M; Parwate, A V; Bhole, A G

2002-01-01

Raw bagasse and fly ash, the waste generated in sugar mills and boilers respectively have been used as low-cost potential adsorbents. Raw bagasse was pretreated with 0.1N NaOH followed by 0.1N CH3COOH before its application. These low-cost adsorbents were used for the removal of chromium and nickel from an aqueous solution. The kinetics of adsorption and extent of adsorption at equilibrium are dependent on the physical and chemical characteristics of the adsorbent, adsorbate and experimental system. The effect of hydrogen ion concentration, contact time, sorbent dose, initial concentrations of adsorbate and adsorbent and particle size on the uptake of chromium and nickel were studied in batch experiments. The Sorption data has been correlated with Langmuir, Freundlich and Bhattacharya and Venkobachar adsorption models. The efficiencies of adsorbent materials for the removal of Cr(VI) and Ni(II) were found to be between 56.2 and 96.2% and 83.6 and 100%, respectively. These results were obtained at the optimized conditions of pH, contact time, sorbent dose, sorbate concentration of 100 mg/l and with the variation of adsorbent particles size between 0.075 and 4.75 mm. The order of selectivity is powdered activated carbon > bagasse > fly ash for Cr(VI) removal and powdered activated carbon > fly ash > bagasse for Ni(II) removal.

Biochars derived from wasted marine macro-algae (Saccharina japonica and Sargassum fusiforme) and their potential for heavy metal removal in aqueous solution.

Science.gov (United States)

Poo, Kyung-Min; Son, Eun-Bi; Chang, Jae-Soo; Ren, Xianghao; Choi, Yun-Jung; Chae, Kyu-Jung

2018-01-15

For the purpose of reusing wasted marine macro-algae generated during cultivation, harvesting, processing and selling processes, biochars derived from Saccharina japonica (known as kelp) and Sargassum fusiforme (known as hijikia) were characterized and their removal capacities for Cu, Cd, and Zn in aqueous solution were assessed. Feedstocks, S. japonica, S. fusiforme, and also pinewood sawdust as a control, were pyrolyzed at 250, 400, 500, 600 and 700 °C. In evaluating heavy metal removal capacities, SJB (S. japonica biochar) showed the best performance, with removal efficiencies of more than 98% for the three heavy metals when pyrolyzed at over 400 °C. SFB (S. fusiforme biochar) also showed good potential as an adsorbent, with removal efficiencies for the three heavy metals of more than 86% when pyrolyzed at over 500 °C. On the contrary, the maximum removal efficiencies of PSB (pinewood sawdust biochar) were 81%, 46%, and 47% for Cu, Cd, and Zn, respectively, even at 700 °C, the highest pyrolysis temperature. This demonstrates that marine macro-algae were advantageous in terms of production energy for removing heavy metals even at relatively low pyrolysis temperatures, compared with PSB. The excellent heavy metal adsorption capacities of marine macro-algae biochars were considered due to their higher pH and more oxygen-containing functional groups, although the specific surface areas of SJB and SFB were significantly lower than that of PSB. This research confirmed that the use of marine macro-algae as a heavy metal adsorbent was suitable not only in the removal of heavy metals, but also in terms of resource recycling and energy efficiency. Copyright © 2017 Elsevier Ltd. All rights reserved.

Removing efficiency of radon from water by different methods

International Nuclear Information System (INIS)

Muellerova, M.; Holy, K.; Gulasova, Z.; Polaskova, A.

2008-01-01

In this contribution problem of radon removing from water samples by different methods was tested. Lowest efficiency of deemanation was achieved at tossing of water from one vessel into the other. For increasing of efficiency deemanation of radon use of needle-bath principle was also used. Low efficiency deemanation was found at trapping of radon from sample of water by toluene (83 ± 5) %, too. Reversal highest efficiency deemanation of radon from water was reached at aerating by argon (95 ± 6)%. It is shown, that reduction of volume activity of radon in water under 0.1 Bq/dm l - 3 is big problem. Suppression of this limit will claim use of more completion and sophistic approaches. (author)

The importance of temporal inequality in quantifying vegetated filter strip removal efficiencies

Science.gov (United States)

Gall, H. E.; Schultz, D.; Mejia, A.; Harman, C. J.; Raj, C.; Goslee, S.; Veith, T.; Patterson, P. H.

2017-12-01

Vegetated filter strips (VFSs) are best management practices (BMPs) commonly implemented adjacent to row-cropped fields to trap overland transport of sediment and other constituents often present in agricultural runoff. VFSs are generally reported to have high sediment removal efficiencies (i.e., 70 - 95%); however, these values are typically calculated as an average of removal efficiencies observed or simulated for individual events. We argue that due to: (i) positively correlated sediment concentration-discharge relationships; (ii) strong temporal inequality exhibited by sediment transport; and (iii) decreasing VFS performance with increasing flow rates, VFS removal efficiencies over annual time scales may be significantly lower than the per-event values or averages typically reported in the literature and used in decision-making models. By applying a stochastic approach to a two-component VFS model, we investigated the extent of the disparity between two calculation methods: averaging efficiencies from each event over the course of one year, versus reporting the total annual load reduction. We examined the effects of soil texture, concentration-discharge relationship, and VFS slope to reveal the potential errors that may be incurred by ignoring the effects of temporal inequality in quantifying VFS performance. Simulation results suggest that errors can be as low as 20%, with the differences between the two methods of removal efficiency calculations greatest for: (i) soils with high percentage of fine particulates; (ii) VFSs with higher slopes; and (iii) strongly positive concentration-discharge relationships. These results can aid in annual-scale decision making for achieving downstream water quality goals.

Ammonia nitrogen removal from aqueous solution by local agricultural wastes

Science.gov (United States)

Azreen, I.; Lija, Y.; Zahrim, A. Y.

2017-06-01

Excess ammonia nitrogen in the waterways causes serious distortion to environment such as eutrophication and toxicity to aquatic organisms. Ammonia nitrogen removal from synthetic solution was investigated by using 40 local agricultural wastes as potential low cost adsorbent. Some of the adsorbent were able to remove ammonia nitrogen with adsorption capacity ranging from 0.58 mg/g to 3.58 mg/g. The highest adsorption capacity was recorded by Langsat peels with 3.58 mg/g followed by Jackfruit seeds and Moringa peels with 3.37 mg/g and 2.64 mg/g respectively. This experimental results show that the agricultural wastes can be utilized as biosorbent for ammonia nitrogen removal. The effect of initial ammonia nitrogen concentration, pH and stirring rate on the adsorption process were studied in batch experiment. The adsorption capacity reached maximum value at pH 7 with initial concentration of 500 mg/L and the removal rate decreased as stirring rate was applied.

Characterization of Cr(VI) removal from aqueous solutions by a surplus agricultural waste-Rice straw

International Nuclear Information System (INIS)

Gao Hui; Liu Yunguo; Zeng Guangming; Xu Weihua; Li Ting; Xia Wenbin

2008-01-01

The removal of Cr(VI) from aqueous solution by rice straw, a surplus agricultural byproduct was investigated. The optimal pH was 2.0 and Cr(VI) removal rate increased with decreased Cr(VI) concentration and with increased temperature. Decrease in straw particle size led to an increase in Cr(VI) removal. Equilibrium was achieved in about 48 h under standard conditions, and Cr(III), which appeared in the solution and remained stable thereafter, indicating that both reduction and adsorption played a part in the Cr(VI) removal. The increase of the solution pH suggested that protons were needed for the Cr(VI) removal. A relatively high level of NO 3 - notably restrained the reduction of Cr(VI) to Cr(III), while high level of SO 4 2- supported it. The promotion of the tartaric acid modified rice straw (TARS) and the slight inhibition of the esterified rice straw (ERS) on Cr(VI) removal indicated that carboxyl groups present on the biomass played an important role in chromium remediation even though were not fully responsible for it. Isotherm tests showed that equilibrium sorption data were better represented by Langmuir model and the sorption capacity of rice straw was found to be 3.15 mg/g

Zinc, nickel, and cobalt ions removal from aqueous solution and plating plant wastewater by modified Aspergillus flavus biomass: A dataset

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Rauf Foroutan

2017-06-01

Full Text Available The biomass of Aspergillus flavus was modified by calcium chloride to achieve a bioadsorbent for treating nickel, cobalt, and zinc ions from aqueous solutions. The information of pH, bioadsorbent dose, contact time, and temperature effect on the removal efficiency are presented. The data of Freundlich and Langmuir isotherm and pseudo-first-order and pseudo-second-order kinetic models are also depicted. The data showed that the maximum bioadsorption capacity of nickel, cobalt, and zinc ions is 32.26, 31.06 and 27.86 mg/g, respectively. The suitability of the bioadsorbent in heavy metals removal at field condition was tested with a real wastewater sample collected from a plating plant in the final part of this dataset. Based on the findings, the bioadsorbent was shown to be an affordable alternative for the removal of metals in the wastewater.

Effective removal of heavy metal ions Cd2+, Zn2+, Pb2+, Cu2+ from aqueous solution by polymer-modified magnetic nanoparticles

International Nuclear Information System (INIS)

Ge, Fei; Li, Meng-Meng; Ye, Hui; Zhao, Bao-Xiang

2012-01-01

We prepared novel Fe 3 O 4 magnetic nanoparticles (MNPs) modified with 3-aminopropyltriethoxysilane (APS) and copolymers of acrylic acid (AA) and crotonic acid (CA). The MNPs were characterized by transmission electron microscopy, X-ray diffraction, infra-red spectra and thermogravimetric analysis. We explored the ability of the MNPs for removing heavy metal ions (Cd 2+ , Zn 2+ , Pb 2+ and Cu 2+ ) from aqueous solution. We investigated the adsorption capacity of Fe 3 O 4 -APS-AA-co-CA at different pH in solution and metal ion uptake capacity as a function of contact time and metal ion concentration. Moreover, adsorption isotherms, kinetics and thermodynamics were studied to understand the mechanism of the synthesized MNPs adsorbing metal ions. In addition, we evaluated the effect of background electrolytes on the adsorption. Furthermore, we explored desorption and reuse of MNPs. Fe 3 O 4 -APS-AA-co-CA MNPs are excellent for removal of heavy metal ions such as Cd 2+ , Zn 2+ , Pb 2+ and Cu 2+ from aqueous solution. Furthermore, the MNPs could efficiently remove the metal ions with high maximum adsorption capacity at pH 5.5 and could be used as a reusable adsorbent with convenient conditions.

Zero-valent iron nanoparticles embedded into reduced graphene oxide-alginate beads for efficient chromium (VI) removal.

Science.gov (United States)

Lv, Xiaoshu; Zhang, Yuling; Fu, Wenyang; Cao, Jiazhen; Zhang, Jiao; Ma, Hanbo; Jiang, Guangming

2017-11-15

Zero-valent iron nanoparticles (Fe 0 NPs) technologies are often challenged by poor dispersibility, chemical instability to oxidation, and mobility during processing, storage and use. This work reports a facile approach to synthesize Fe 0 NPs embedded reduced graphene oxide-alginate beads (Fe@GA beads) via the immobilization of pre-synthesized Fe 0 NPs into graphene oxide modified alginate gel followed by a modelling and in-situ reduction process. The structure/composition characterization of the beads finds that the graphene sheets and the Fe 0 NPs (a shape of ellipsoid and a size of beads. We demonstrate that these Fe@GA beads show a robust performance in aqueous Cr(VI) removal. With a optimized Fe and alginate content, Fe@GA bead can achieve a high Cr(VI) removal efficiency and an excellent mechanical strength. The initial Cr(VI) concentration, ionic strength, temperature and especially solution pH are all critical factors to control the Fe@GA beads performance in Cr(VI) removal. Fitness of the pseudo second-order adsorption model with data suggests adsorption is the rate-controlling step, and both Langmuir and Freundlich adsorption isotherm are suitable to describe the removal behavior. The possible Cr(VI) removal path by Fe@GA beads is put forward, and the synergistic effect in this ternary system implies the potentials of Fe@GA beads in pollutant removal from water body. Copyright © 2017 Elsevier Inc. All rights reserved.

Comparison of Electrocoagulation and Chemical Coagulation Processes in Removing Reactive red 196 from Aqueous Solution

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Ali Assadi

2016-06-01

Full Text Available Background: Conventional chemical coagulation is considered as an old method to dye and COD removal in textile effluent. Electrocoagulation (EC process is a robust method to achieve maximum removal. Methods: This study was designed to compare the result of operational parameters including optimum pH and coagulant concentration for chemical coagulation with ferric chloride and alum also, voltage, electrolysis time, initial pH, and conductivity for EC with iron electrodes to remove reactive red 196 (RR 196. Results: The outcomes show that ferric chloride and alum at optimum concentration were capable of removing dye and COD by 79.63 % and 84.83% and 53% and 55%, respectively. In contrast, EC process removed the dye and COD by 99.98% and 90.4%, respectively. Conclusion: The highest treatment efficiency was obtained by increasing the voltage, electrolysis time, pH and conductivity. Increase initial dye concentration reduces removal efficiency. Ultimately, it could be concluded that EC technology is an efficient procedure for handling of colored industrial wastewaters.

Sludge Recycle of Wastewater Treatment Plant via its Application as Powdered Activated Carbon for Removal of Methyl Tertiary-Butyl Ether (MTBE from Aqueous Solutions

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MR Zare

2016-05-01

Full Text Available Introduction: Nowadays, application of MTBE due to its physical and chemical characteristics including high solubility in water has been increased, resulting in its release into the water resources. On other hand, waste activated sludge derived from municipal wastewater treatment plant (MWTP contains high amount of carbon. Therefore, this study aimed to provide the activated carbon via sludge of MWTP as well as to evaluate its efficiency for MTBE removal. Methods: The effect of some parameters such as kind of activator, pH (2-10, contact time (0-240min, adsorbent dose (2-6g/L and initial concentration of MTBE (20-70mg/L was investigated on MTBE adsorption via activated carbon, after preparation of coal from wastewater sludge and activation of this coal via 3 molar solution of H2PO4,  and KOH as well as 5 molar solution of ZnCl2. MTBE concentration in solution was determined via Gas-Chromatography instrument. The obtained experimental data were modeled by adsorption model of Freundlich and Langmuir. Results: The maximum adsorbed MTBE per gram of activated carbon was obtained when the ZnCL2 was used as an activator; however, there was no statistically significant difference among different activators. In addition, maximum removal efficiency (about 50% was obtained in acidic pH of 4, 6g/L of activated carbon and 20mg/L of MTBE concentration. Results of adsorption isotherm showed that Freundlich adsorption model had a better compliance with the experimental data. Conclusion: Regarding the problems associated with sludge disposal of wastewater treatment plant, recycling of this sludge, as an adsorbent, can eliminate most of these problems. As a result, the economical features with respect to industrial scale application and the efficiency of this substance in removal of other pollutants are recommended to be investigated.

Removal of chromium (VI) ions from aqueous solutions using amine-impregnated TiO2 nanoparticles modified cellulose acetate membranes.

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Gebru, Kibrom Alebel; Das, Chandan

2018-01-01

In this work, TiO 2 nanoparticles (NPs) were modified using tetraethylenepentamine (TEPA), ethylenediamine (EDA), and hexamethylenetetramine (HMTA) amines using impregnation process. The prepared amine modified TiO 2 samples were explored as an additive to fabricate ultrafiltration membranes with enhanced capacity towards the removal of chromium ions from aqueous solution. Modified membranes were prepared from cellulose acetate (CA) polymer blended with polyethylene glycol (PEG) additive, and amine modified TiO 2 by using phase inversion technique. Fourier transform infrared spectroscopy (FTIR), zeta potential (ζ), thermo gravimetric analysis (TGA), field emission scanning electron microscopy (FESEM), water contact angle (WCA), and atomic absorption spectrophotometer (AAS) studies were done to characterize the membranes in terms of chemical structure, electric charge, thermal stability, morphology, hydrophilicity, and removal performance. The pure water permeability and Cr (VI) ion removal efficiency of the unmodified (i.e. CA/U-Ti) and the amine modified (CA/Ti-HMTA, CA/Ti-EDA, and CA/Ti-TEPA) membranes were dependent on pH and metal ion concentration. Incorporation of amine modified TiO 2 composite to the CA polymer was found to improve the fouling and removal characteristics of the membranes during the chromium ultrafiltration process. The maximum removal efficiency result of Cr (VI) ions at pH of 3.5 using CA/Ti-TEPA membrane was 99.8%. The washing/regeneration cycle results in this study described as an essential part for prospect industrial applications of the prepared membranes. The maximum Cr (VI) removal results by using CA/Ti-TEPA membrane for four washing/regeneration cycles are 99.6%, 99.5%, 98.6% and, 96.6%, respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

Phosphate removal from aqueous solutions using polyaniline/ Ni 0.5 Zn 0.5 Fe 2 O 4 magnetic nanocomposite

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Mohammad Hossein Tarmahi

2017-05-01

Full Text Available Background: Phosphorus is an indispensable element for the growth of animals and plants. There are several environmental problems related to phosphate; therefore, the technical and economic methods of removing phosphate are of great importance. This study evaluated the efficiency of polyaniline/ Ni0.5Zn0.5Fe2O4 magnetic nanocomposite in removing phosphate from aqueous environments. Methods: The adsorbent was characterized by several methods, including X-ray diffraction (XRD, scanning electron microscopy (SEM, vibrating sample magnetometer (VSM, and Fourier transform infrared (FT-IR spectroscopy. Then, the potential of the adsorbentto adsorb phosphate was investigated. The effects of the parameters of contact time (5-60 minutes, pH (3-9, adsorbent dosage (0.05-0.6 g, and initial phosphate concentration (2-100 mg/L on the phosphate removal yield were studied. All phosphate ion concentrations were measured using the ammonium molybdate spectrophotometric method. Results: The results showed that a time of 30 minutes, pH of 5, and adsorbent dose of 0.4 g were the optimum conditions for phosphate removal through adsorption. Increasing the initial concentration of phosphate from 2 to 100 mg/L decreased the removal efficiency from 90.3% to 32%. The experimental data was fitted well with the Freundlich isotherm model (R2 = 0.997. Conclusion: Polyaniline/Ni0.5Zn0.5Fe2O4 magnetic nanocomposite removes phosphate from aqueous solutions with a simple and environmentally benign procedure. The maximum adsorption capacity based on Langmuir isotherm (R2 = 0.931 is 85.4 mg/g. This magnetic nanocomposite is applicable in managing water resource pollution caused by phosphate ions.

Cadmium Removal from Aqueous Solutions by Ground Pine Cone

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H Izanloo, S Nasseri

2005-01-01

Full Text Available A study on the removal of cadmium ions from aqueous solutions by pine cone was conducted in batch conditions. Kinetic data and equilibrium removal isotherms were obtained. The influence of different experimental parameters such as contact time, initial concentration of cadmium, pine cone mass and particle size, and temperature on the kinetics of cadmium removal was studied. Results showed that the main parameters that played an important role in removal phenomenon were initial cadmium concentration, particle size and pine cone mass. The necessary time to reach equilibrium was between 4 and 7 hours based on the initial concentration of cadmium. The capacity of cadmium adsorption at equilibrium increased with the decrease of pine cone particle size. The capacity of cadmium adsorption at equilibrium by pine cone increased with the quantity of pine cone introduced (1–4 g/L. Temperature in the range of 20-30°C showed a restricted effect on the removal kinetics (13.56 mg/g at 20°C and a low capacity of adsorption about 11.48 mg/g at 30°C. The process followed pseudo second-order kinetics. The cadmium uptake of pine cone was quantitatively evaluated using adsorption isotherms. Results indicated that the Langmuir model gave a better fit to the experimental data in comparison with the Freundlich equation.

Simultaneous cadmium removal and 2,4-dichlorophenol degradation from aqueous solutions by Phanerochaete chrysosporium

Energy Technology Data Exchange (ETDEWEB)

Chen, Anwei; Zeng, Guangming; Chen, Guiqiu; Fan, Jiaqi; Zou, Zhengjun; Li, Hui; Hu, Xinjiang; Long, Fei [Hunan Univ., Changsha (China). College of Environmental Science and Engineering; Ministry of Education, Changsha (CN). Key Lab. of Environmental Biology and Pollution Control (Hunan Univ.)

2011-08-15

Phanerochaete chrysosporium has been recognised as an effective bioremediation agent due to its unique degradation to xenobiotic and biosorption ability to heavy metals. However, few studies have focused on the simultaneous removal of heavy metals and organic pollutants. The aim of this work was to study the feasibility of simultaneous cadmium removal and 2,4-dichlorophenol (2,4-DCP) degradation in P. chrysosporium liquid cultures. The removal efficiencies were pH dependent and the maximum removal efficiencies were observed at pH 6.5 under an initial cadmium concentration of 5 mg/L and an initial 2,4-DCP concentration of 20 mg/L. The removal efficiencies for cadmium and 2,4-DCP reached 63.62% and 83.90%, respectively, under the optimum conditions. The high production levels of lignin peroxidase (7.35 U/mL) and manganese peroxidase (8.30 U/mL) resulted in an increase in 2,4-DCP degradation. The protein content decreased with increasing cadmium concentration. The surface characteristics and functional groups of the biomass were studied by scanning electron microscopy and a Fourier-transformed infrared spectrometer. The results showed that the use of P. chrysosporium is promising for the simultaneous removal of cadmium and 2,4-DCP from liquid media. (orig.)

High efficiency particulate removal with sintered metal filters

International Nuclear Information System (INIS)

Kirstein, B.E.; Paplawsky, W.J.; Pence, D.T.; Hedahl, T.G.

1981-01-01

Because of their particle removal efficiencies and durability, sintered metal filters have been chosen for high efficiency particulate air (HEPA) filter protection in the off-gas treatment system for the proposed Idaho National Engineering Laboratory Transuranic Waste Treatment Facility. Process evaluation of sintered metal filters indicated a lack of sufficient process design data to ensure trouble-free operation. Subsequence pilot scale testing was performed with flyash as the test particulate. The test results showed that the sintered metal filters can have an efficiency greater than 0.9999999 for the specific test conditions used. Stable pressure drop characteristics were observed in pulsed and reversed flow blowback modes of operation. Over 4900 hours of operation were obtained with operating conditions ranging up to approximately 90 0 C and 24 vol % water vapor in the gas stream

Preparation and Utilization of Kapok Hull Carbon for the Removal of Rhodamine-B from Aqueous Solution

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P. S. Syed Shabudeen

2006-01-01

Full Text Available A carbonaceous sorbent prepared from the indegeneous agricultural waste (which is facing solid waste disposal problem Kapok Hull, by acid treatment was tested for its efficiency in removing basic dyes. Batch kinetic and isotherm experiments were conducted to determine the sorption and desorption of the Rhodamine-B from aqueous solution with activated carbon. The factors affecting the rate processes involved in the removal of dye for initial dye concentration, agitation time, and carbon dose and particle size have been studied at ambient temperature. The adsorption process followed first order rate kinetics. The first-order rate equation by Lagergren was tested on the kinetic data, and isotherm data was analyzed for possible agreement with the Langmuir and Freundlich adsorption isotherm equations. The intraparticle diffusion rate equation from which adsorption rate constants, diffusion rate constants and diffusion coefficients were determined. Intraparticle diffusion was found to be the rate-limiting step. The structural and morphological of activated carbon were characterized by XRD and SEM studies respectively.

Removal of endocrine disruptors PAEs in drinking water by gamma-ray irradiation

International Nuclear Information System (INIS)

Zhao Yongfu; Zheng Zheng; Zheng Binguo; Wang Changbao; Li Lili

2012-01-01

Phthalic acid esters (PAEs) belong to environmental endocrine disruptor. The dimethyl phthalate (DMP), diethyl phthalate (DEP) and di-n-butyl phthalate (DBP) were selected for the radiation study. The removal efficiencies of DMP, DEP and DBP in drinking water by gamma-ray irradiation are discussed. The results show that these PAEs could be efficiently removed by gamma-ray irradiation. The removal efficiencies of DMP, DEP and DBP (12 mg/L) in aqueous solutions by 0.8 kGy gamma-ray treatment were 96.6%, 94.5% and 86.2%. The absorbed dose needed for the removal of total carbon in aqueous solutions was much larger than the doses for PAEs degradation. When 2 kGy was selected, the removal efficiencies of TC for DMP, DEP and DBP were only 23.6%, 14.3% and 12.9%. The study results also show that the radiation degradation reaction of PAEs should be divided into two stages: low dose addition reaction and high dose ring-opening reaction. This study is of significance in the disposal of micro-polluted drinking water. (authors)

Fabrication of Chitosan-complexed Electrode and Evaluation of Its Efficiency in Removal of Copper Ion from Aqueous Solution

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Yoon Young-Chan

2016-01-01

Full Text Available In this study, we fabricated chitosan/PVA/activated carbon complexed electrode to remove copper ion from aqueous solution. The prepared composite electrode was analyzed by BET and SEM to investigate its physicochemical properties. Electrochemical properties of prepared composite electrodes were analyzed via cyclic voltammetry. Adsorption performance of copper ion on chitosan composite complexed electrodes was evaluated. Almost similar pore size distribution results were observed in the series of ACP not included electrodes while observed differences in pore size distribution for the ACP included one. Cyclic voltammetry results exhibited that oxidation-reduction reaction does not occur in a potential range of -1.0 ~ 1.0 V. The amount of copper ion during adsroption reaction is increase according to increase of adsorption potential to 1.0 V.

One-step synthesis of water-dispersible cysteine functionalized magnetic Fe3O4 nanoparticles for mercury(II) removal from aqueous solutions

International Nuclear Information System (INIS)

Shen, Xiaofang; Wang, Qin; Chen, WenLing; Pang, Yuehong

2014-01-01

Graphical abstract: Using Fe 2+ as precursors, air as oxidant and cysteine as protectant, this novel cysteine functionalized Fe 3 O 4 magnetic nanoparticles (Cys-Fe 3 O 4 MNPs) was facilely one-pot synthesized at room temperature by oxidation–precipitation method with the assistance of sonication. Then the Cys-Fe 3 O 4 MNPs were demonstrated as an inexpensive and quite efficient magnetic nano-adsorbent for as high as 95% Hg(II) removal efficiency. These results indicated that Cys-Fe 3 O 4 MNPs is a potentially attractive material for the removal of Hg(II) from water. - Highlights: • A simplified one-step synthesis method of superparamagnetic Cys-Fe 3 O 4 MNPs was developed. • It was synthesized at room temperature by oxidation-precipitation method with the assistance of sonication. • It was demonstrated as an inexpensive and quite efficient magnetic nano-adsorbent for Hg(II) removal. - Abstract: Cysteine functionalized Fe 3 O 4 magnetic nanoparticles (Cys-Fe 3 O 4 MNPs) were prepared facilely for Hg(II) removal from aqueous solutions. Using Fe 2+ as precursors, air as oxidant and Cys as protectant, this novel material was one-pot synthesis at room temperature by oxidation–precipitation method with the assistance of sonication. The MNPs were characterized by TEM, VSM, FTIR, X-ray powder diffraction analysis (XRD) and TGA methods. Under the optimum experimental conditions, the removal efficiency was as high as 95% and the maximum sorption capacity is found to be 380 mg/mol for Hg(II). Study on adsorption kinetics shows that adsorption of Hg(II) onto Cys-Fe 3 O 4 MNPs follows pseudo-first-order kinetic model and the adsorption rate constant was 0.22 min −1 . Additionally, the Hg(II)-loaded Cys-Fe 3 O 4 MNPs could be easily regenerated up to 95% using 1.0 M acetic acid. These results indicated that Cys-Fe 3 O 4 MNPs is a potentially attractive material for the removal of Hg(II) from water

Fractional Factorial Design Study on the Performance of GAC-Enhanced Electrocoagulation Process Involved in Color Removal from Dye Solutions

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Iuliana Gabriela Breaban

2013-07-01

Full Text Available The aim of this study was to determine the effects of main factors and interactions on the color removal performance from dye solutions using the electrocoagulation process enhanced by adsorption on Granular Activated Carbon (GAC. In this study, a mathematical approach was conducted using a two-level fractional factorial design (FFD for a given dye solution. Three textile dyes: Acid Blue 74, Basic Red 1, and Reactive Black 5 were used. Experimental factors used and their respective levels were: current density (2.73 or 27.32 A/m2, initial pH of aqueous dye solution (3 or 9, electrocoagulation time (20 or 180 min, GAC dose (0.1 or 0.5 g/L, support electrolyte (2 or 50 mM, initial dye concentration (0.05 or 0.25 g/L and current type (Direct Current—DC or Alternative Pulsed Current—APC. GAC-enhanced electrocoagulation performance was analyzed statistically in terms of removal efficiency, electrical energy, and electrode material consumptions, using modeling polynomial equations. The statistical significance of GAC dose level on the performance of GAC enhanced electrocoagulation and the experimental conditions that favor the process operation of electrocoagulation in APC regime were determined. The local optimal experimental conditions were established using a multi-objective desirability function method.

Fractional Factorial Design Study on the Performance of GAC-Enhanced Electrocoagulation Process Involved in Color Removal from Dye Solutions.

Science.gov (United States)

Secula, Marius Sebastian; Cretescu, Igor; Cagnon, Benoit; Manea, Liliana Rozemarie; Stan, Corneliu Sergiu; Breaban, Iuliana Gabriela

2013-07-10

The aim of this study was to determine the effects of main factors and interactions on the color removal performance from dye solutions using the electrocoagulation process enhanced by adsorption on Granular Activated Carbon (GAC). In this study, a mathematical approach was conducted using a two-level fractional factorial design ( FFD ) for a given dye solution. Three textile dyes: Acid Blue 74, Basic Red 1, and Reactive Black 5 were used. Experimental factors used and their respective levels were: current density (2.73 or 27.32 A/m²), initial pH of aqueous dye solution (3 or 9), electrocoagulation time (20 or 180 min), GAC dose (0.1 or 0.5 g/L), support electrolyte (2 or 50 mM), initial dye concentration (0.05 or 0.25 g/L) and current type (Direct Current- DC or Alternative Pulsed Current- APC ). GAC-enhanced electrocoagulation performance was analyzed statistically in terms of removal efficiency, electrical energy, and electrode material consumptions, using modeling polynomial equations. The statistical significance of GAC dose level on the performance of GAC enhanced electrocoagulation and the experimental conditions that favor the process operation of electrocoagulation in APC regime were determined. The local optimal experimental conditions were established using a multi-objective desirability function method.

Efficiency Comparison of Modified-Clay and Lime-Marlin the Adsorption of Fluoride from Aqueous Solution

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Mohammad Taghi Samadi

2016-06-01

Full Text Available Background and purpose: Fluoride is one of the common anion in water that its concentration varies in different water supplies. Most of the body's requirement for fluoride is supplied through drinking water. Fluoride in low concentration is essential for human health but in high concentration is very hazardous for human health. The efficiency of modified-clay and lime-marl were investigated in this research as an adsorbent for the elimination of fluoride from aqueou solution.  Methods: In this study, the capability of modified-clay and lime-marl to adsorb fluoride ions was conducted using a series of batch tests in a shaker-incubator instrument. The effect of experimental parameters such as pH (4,7,10,  adsorbent dosage (1,5,10 g/L, initial fluoride concentration  (5,10,15 mg/L andcontact time (15-120 min were evaluated. The morphological and micro-structural character of  modified-clay and lime-marl have performed by using X-ray diffraction (XRD. The formation of the carboxylic functional groups was verified by Fourier transform infrared spectra (FT-IR.  Findings: results well demonstrate higher removal efficiency of fluoride was 95.23% and 28.71 by clay-modified and lime-marl, respectively; at 10 mg/L of fluoride concentration and 60 min contact time. The adsorption kinetics fitted well using the pseudo second-order kinetic model; however, equlibrium data were best fitted onto Langmiur isotherm model. The maximum adsorption capacities of modified-clay and lime-marl for fluoride were found to be 4.43 mg/g and 1.32 mg/g, respectively. Conclusion: According to our finding, it proposed that adsorption process by using modified clay is very efficient and economic process for fluoride removal from aqueous solution.

Comparison between Removal Efficiency of Slag, zeolite, and Conventional media in slow sand Filter for Removal of Lead and Cadmium from Water Resources

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A Ebrahimi

2016-03-01

Full Text Available Introduction: Heavy metals owing to their health hazards and high toxicity in low concentration for human and environment have very concern and attention. Slow sand filter is one of the simple and cost-effective for removal of these pollutants. In this method, media play an important role for removal of pollutant. Therefore, the aim of this study was investigation of different media like slag, zeolite, and conventional media in slow sand filter for removal of lead and cadmium. Methods: In this research there are three beds filter include typical filter bed, slag and zeolite that used in pilot plant for investigation of lead and cadmium removal at three concentration of 0.1T 1 and 10 ppm. Each of filters has an internal diameter of 8 cm and a height of 120 cm with Plexiglas, which have a continuous flow operation. Results: The removal efficiency of turbidity by three typical filter bed, slag, and zeolite with initial turbidity of 13 NTU was 46%, 77%, and 89% respectively. Removal efficiency of lead without turbidity was 70.3%, 79%, and 59.8% respectively for 0.1 ppm lead. For 1 ppm, concentration of lead removal efficiency was 51.8%, 52.7% and 52.6% respectively and for 10 ppm it was 53.4%, 57.8%, and 59.8% respectively. Cadmium removal for these media was 23.4%, 37.5%, and 59.4% respectively at 0.1 ppm cadmium. At 1 ppm of cadmium concentration, it was 37.9%, 45% and 41.3% respectively and at 10 ppm concentration of cadmium it was 68.3%, 68.6% and 67% respectively. Conclusion: Slag and zeolite beds are more efficiently than the conventional sand beds in the slow sand filter, so it can be used instead of the usual sand for removing lead and cadmium from resources water.

Assessment of Pb (II Removal from Aqueous Solutions by Ascorbic Acid-stabilized Zero-valent Iron Nanoparticles Using Response Surface Methodology (RSM

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Mohaddeseh Savasari

2017-07-01

Full Text Available The growing pollution of water resources and the limited availability of water supplies have led to a growing interest by researchers to develop novel methods of water remediation and reuse. One such method is the use of ascorbic acid-stabilized zero-valent iron nanoparticles (AAS-ZVIN for the removal of lead (Pb from aqueous solutions. Using zero-valent iron nanoparticles stabilized with acid ascorbic under aerobic conditions, the present study was conducted to assess the efficiency of Pb removal from aqueous solutions and its optimization by the response surface methodology (RSM. For this purpose, use was made of the central composite design and the response surface methodology with the four input variables of ASS- ZVIN dose (0.5, 1, and 2 g L-1, pH (2, 5, and 7, contact time (5, 20, and 60 min, and initial Pb concentration (5, 10, and 20 mg L-1 to determine the optimal conditions for the process. Numerical optimization revealed that the optimum conditions for Pb removal (97.93% included an ASS-ZVIN dose of 2 g L-1, an initial Pb (II concentration of 25 mg L-1, a contact time of 60 min, and an initial solution pH of 7. The results also imply that not only does ASS-ZVIN offer a good potential for the remediation of water bodies contaminated with Pb, given its high reactivity for Pb removal, but that  the RSM optimization process can be successfully employed for the optimization of the process in question.

Removal of Cr(VI and Toxic Ions from Aqueous Solutions and Tannery Wastewater Using Polymer-Clay Composites

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Abd El-Azeem Sallam

2017-10-01

Full Text Available Polymer-clay composites were prepared by natural zeolite (clinoptilolite or naturally local clay deposits in an N,N-methylene-bis-acrylamide as cross-linked. The resultant composites were used for the removal of Cr(VI from an aqueous solution. Additionally, their effects on soluble ions of tannery wastewater were investigated. The produced composites were characterized using X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FT-IR, and scanning electron microscopy (SEM. The results showed that Cr(VI removal is dependent upon initial concentrations and pH. The adsorption quantity of Cr(VI onto the polymerized clay deposit followed by polymerized zeolite exhibited higher values than their original samples. The polymer-clay composite of clay deposit showed the highest removal of 76.3–100% overall initial concentrations of 10–50 mg L−1 and at initial pH of 2. Kinetics of Cr(VI removal by various sorbents was predicted using a pseudo–second order model. Our findings showed that the levels of salinity and various soluble ions (Cr2+, Na+, Cl− and SO42− in tannery wastewater are very high, and their levels were reduced after treatment, especially by polymerized sorbents. It could be concluded that the polymer-clay composites may be employed as a highly efficient sorbent for the removal of Cr(VI and toxic ions from the wastewater.

The Use of Sonochemical Technology for Cyanide Removal from Aqueous Solutions in the Presence of Hydrogen Peroxide

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Reza Shokoohi

2011-10-01

Full Text Available Cyanide is a highly toxic species that found mostly in industrial effluents such as electroplating, metal mining, metallurgy and metal cleaning processes. Discharge of it into the enviroment causes very health impact. Purpose of this study was, determination of sonochemical technology for cyanide removal from aqueous solutions in the presence of hydrogen peroxide. In this study, a productive set of 500w power ultresoun waves with two frequencies 35 kHz and 130 kHz were used. Experiments were performed using different initial ratio CN-/H2O2 1/1, 1/3 and 1/5 and at initial cyanide concentrations varying from 2.5 to 75 mg/L. The effects of parameters such as pH, time and initial cyanide concentration on the sonochemical degradation have been studied. The results of the study showed that the maximom removal efficiency of cyanide was achieved 85% by sonochemical technology at frequency of 130 kHz, during of 90 min, at pH of 11, at initial cyanide concentration of  2.5 mg/l and with initial ratio of CN-/H2O2 1/5. it was also found the rates of cyanide degradation under different conditions were quite low, and also the rate of cyanide degradation was high at first but later substantially reduced. The efficiency of cyanide removal had direct relationship with pH, frequency, hydrogen peroxide concentration and time ,and it had reverse relationship with cyanide concentration.

Removal of heavy metals from aqueous solutions using Fe{sub 3}O{sub 4}, ZnO, and CuO nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Mahdavi, Shahriar, E-mail: smahdaviha@yahoo.com; Jalali, Mohsen, E-mail: jalali@basu.ac.ir [College of Agriculture, Bu-Ali Sina University, Department of Soil Science (Iran, Islamic Republic of); Afkhami, Abbas, E-mail: afkhami@basu.ac.ir [College of Chemistry, Bu-Ali Sina University, Department of Analytical Chemistry (Iran, Islamic Republic of)

2012-08-15

This study investigated the removal of Cd{sup 2+}, Cu{sup 2+}, Ni{sup 2+}, and Pb{sup 2+} from aqueous solutions with novel nanoparticle sorbents (Fe{sub 3}O{sub 4}, ZnO, and CuO) using a range of experimental approaches, including, pH, competing ions, sorbent masses, contact time, scanning electron microscopy, transmission electron microscopy, and X-ray diffraction. The images showed that Fe{sub 3}O{sub 4}, ZnO, and CuO particles had mean diameters of about 50 nm (spheroid), 25 nm (rod shape), and 75 nm (spheroid), respectively. Tests were performed under batch conditions to determine the adsorption rate and uptake at equilibrium from single and multiple component solutions. The maximum uptake values (sum of four metals) in multiple component solutions were 360.6, 114.5, and 73.0 mg g{sup -1}, for ZnO, CuO, and Fe{sub 3}O{sub 4}, respectively. Based on the average metal removal by the three nanoparticles, the following order was determined for single component solutions: Cd{sup 2+} > Pb{sup 2+} > Cu{sup 2+} > Ni{sup 2+}, while the following order was determined in multiple component solutions: Pb{sup 2+} > Cu{sup 2+} > Cd{sup 2+} > Ni{sup 2+}. Sorption equilibrium isotherms could be described using the Freundlich model in some cases, whereas other isotherms did not follow this model. Furthermore, a pseudo-second order kinetic model was found to correctly describe the experimental data for all nanoparticles. Scanning electron microscopy, energy dispersive X-ray before and after metal sorption, and soil solution saturation indices showed that the main mechanism of sorption for Cd{sup 2+} and Pb{sup 2+} was adsorption, whereas both Cu{sup 2+} and Ni{sup 2+} sorption were due to adsorption and precipitation. These nanoparticles have potential for use as efficient sorbents for the removal of heavy metals from aqueous solutions and ZnO nanoparticles were identified as the most promising sorbent due to their high metal uptake.

Efficiency of WWTP to remove emerging pollutants in wastewater